Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 4924 |
| ensemblid | ENSG00000104805.17 |
| hgncid | 8043 |
| symbol | NUCB1 |
| name | nucleobindin 1 |
| refseq_nuc | NM_006184.6 |
| refseq_prot | NP_006175.2 |
| ensembl_nuc | ENST00000405315.9 |
| ensembl_prot | ENSP00000385923.3 |
| mane_status | MANE Select |
| chr | chr19 |
| start | 48900312 |
| end | 48923372 |
| strand | + |
| ver | v1.2 |
| region | chr19:48900312-48923372 |
| region5000 | chr19:48895312-48928372 |
| regionname0 | NUCB1_chr19_48900312_48923372 |
| regionname5000 | NUCB1_chr19_48895312_48928372 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 461 | 387 | 91 | 73 | 168 | 15 | 38 | 120 | NUCB1_chr19_48895312_48928372 | NUCB1 | MPPSG others(456): Show |
chr19 | 48895312 | 48928372 |
| a0002 | 0/0 | 461 | 7 | 7 | 0 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | MPPSG others(456): Show |
chr19 | 48895312 | 48928372 |
| a0003 | 0/0 | 461 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | MPPSG others(456): Show |
chr19 | 48895312 | 48928372 |
| a0004 | 0/0 | 461 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | MPPSG others(456): Show |
chr19 | 48895312 | 48928372 |
| a0005 | 0/0 | 457 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NUCB1_chr19_48895312_48928372 | NUCB1 | MPPSG others(452): Show |
chr19 | 48895312 | 48928372 |
| a0006 | 0/0 | 461 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NUCB1_chr19_48895312_48928372 | NUCB1 | MPPSG others(456): Show |
chr19 | 48895312 | 48928372 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1383 | 352 | 76 | 62 | 166 | 12 | 34 | NUCB1_chr19_48895312_48928372 | NUCB1 | ATGCC others(1378): Show |
chr19 | 48895312 | 48928372 | ||
| a0001c0002 | 0/0 | 1383 | 15 | 1 | 9 | 0 | 3 | 2 | NUCB1_chr19_48895312_48928372 | NUCB1 | ATGCC others(1378): Show |
chr19 | 48895312 | 48928372 | ||
| a0001c0003 | 0/0 | 1383 | 15 | 13 | 2 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | ATGCC others(1378): Show |
chr19 | 48895312 | 48928372 | ||
| a0001c0005 | 0/0 | 1383 | 2 | 0 | 0 | 2 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | ATGCC others(1378): Show |
chr19 | 48895312 | 48928372 | ||
| a0001c0007 | 0/0 | 1383 | 1 | 0 | 0 | 0 | 0 | 1 | NUCB1_chr19_48895312_48928372 | NUCB1 | ATGCC others(1378): Show |
chr19 | 48895312 | 48928372 | ||
| a0001c0008 | 0/0 | 1383 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | ATGCC others(1378): Show |
chr19 | 48895312 | 48928372 | ||
| a0001c0011 | 0/0 | 1383 | 1 | 0 | 0 | 0 | 0 | 1 | NUCB1_chr19_48895312_48928372 | NUCB1 | ATGCC others(1378): Show |
chr19 | 48895312 | 48928372 | ||
| a0002c0004 | 0/0 | 1383 | 7 | 7 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | ATGCC others(1378): Show |
chr19 | 48895312 | 48928372 | ||
| a0003c0006 | 0/0 | 1383 | 1 | 0 | 0 | 0 | 1 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | ATGCC others(1378): Show |
chr19 | 48895312 | 48928372 | ||
| a0004c0012 | 0/0 | 1383 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | ATGCC others(1378): Show |
chr19 | 48895312 | 48928372 | ||
| a0005c0009 | 0/0 | 1371 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | ATGCC others(1366): Show |
chr19 | 48895312 | 48928372 | ||
| a0006c0010 | 0/0 | 1383 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | ATGCC others(1378): Show |
chr19 | 48895312 | 48928372 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 2406 | 170 | 47 | 15 | 93 | 2 | 13 | NUCB1_chr19_48895312_48928372 | NUCB1 | ACCAA others(2401): Show |
chr19 | 48895312 | 48928372 |
| a0001c0001t0002 | 0/1 | 2406 | 140 | 7 | 40 | 64 | 10 | 18 | NUCB1_chr19_48895312_48928372 | NUCB1 | ACCAA others(2401): Show |
chr19 | 48895312 | 48928372 |
| a0001c0001t0003 | 1/0 | 2406 | 15 | 3 | 2 | 7 | 0 | 2 | NUCB1_chr19_48895312_48928372 | NUCB1 | ACCAA others(2401): Show |
chr19 | 48895312 | 48928372 |
| a0001c0001t0004 | 0/0 | 2406 | 6 | 6 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | ACCAA others(2401): Show |
chr19 | 48895312 | 48928372 |
| a0001c0001t0005 | 0/0 | 2406 | 5 | 0 | 3 | 2 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | ACCAA others(2401): Show |
chr19 | 48895312 | 48928372 |
| a0001c0001t0006 | 0/0 | 2406 | 4 | 4 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | ACCAA others(2401): Show |
chr19 | 48895312 | 48928372 |
| a0001c0001t0007 | 0/0 | 2406 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | ACCAA others(2401): Show |
chr19 | 48895312 | 48928372 |
| a0001c0001t0008 | 0/0 | 2406 | 2 | 2 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | ACCAA others(2401): Show |
chr19 | 48895312 | 48928372 |
| a0001c0001t0009 | 0/0 | 2406 | 2 | 1 | 1 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | ACCAA others(2401): Show |
chr19 | 48895312 | 48928372 |
| a0001c0001t0010 | 0/0 | 2406 | 2 | 2 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | ACCAA others(2401): Show |
chr19 | 48895312 | 48928372 |
| a0001c0001t0011 | 0/0 | 2406 | 1 | 0 | 0 | 0 | 0 | 1 | NUCB1_chr19_48895312_48928372 | NUCB1 | ACCAA others(2401): Show |
chr19 | 48895312 | 48928372 |
| a0001c0001t0013 | 0/0 | 2406 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | ACCAA others(2401): Show |
chr19 | 48895312 | 48928372 |
| a0001c0001t0014 | 0/0 | 2406 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | ACCAA others(2401): Show |
chr19 | 48895312 | 48928372 |
| a0001c0001t0015 | 0/0 | 2406 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | ACCAA others(2401): Show |
chr19 | 48895312 | 48928372 |
| a0001c0001t0016 | 0/0 | 2406 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | ACCAA others(2401): Show |
chr19 | 48895312 | 48928372 |
| a0001c0002t0001 | 0/0 | 2406 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | ACCAA others(2401): Show |
chr19 | 48895312 | 48928372 |
| a0001c0002t0002 | 0/0 | 2406 | 12 | 1 | 6 | 0 | 3 | 2 | NUCB1_chr19_48895312_48928372 | NUCB1 | ACCAA others(2401): Show |
chr19 | 48895312 | 48928372 |
| a0001c0002t0007 | 0/0 | 2406 | 2 | 0 | 2 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | ACCAA others(2401): Show |
chr19 | 48895312 | 48928372 |
| a0001c0003t0001 | 0/0 | 2406 | 15 | 13 | 2 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | ACCAA others(2401): Show |
chr19 | 48895312 | 48928372 |
| a0001c0005t0001 | 0/0 | 2406 | 2 | 0 | 0 | 2 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | ACCAA others(2401): Show |
chr19 | 48895312 | 48928372 |
| a0001c0007t0001 | 0/0 | 2406 | 1 | 0 | 0 | 0 | 0 | 1 | NUCB1_chr19_48895312_48928372 | NUCB1 | ACCAA others(2401): Show |
chr19 | 48895312 | 48928372 |
| a0001c0008t0012 | 0/0 | 2406 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | ACCAA others(2401): Show |
chr19 | 48895312 | 48928372 |
| a0001c0011t0002 | 0/0 | 2406 | 1 | 0 | 0 | 0 | 0 | 1 | NUCB1_chr19_48895312_48928372 | NUCB1 | ACCAA others(2401): Show |
chr19 | 48895312 | 48928372 |
| a0002c0004t0001 | 0/0 | 2406 | 7 | 7 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | ACCAA others(2401): Show |
chr19 | 48895312 | 48928372 |
| a0003c0006t0007 | 0/0 | 2406 | 1 | 0 | 0 | 0 | 1 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | ACCAA others(2401): Show |
chr19 | 48895312 | 48928372 |
| a0004c0012t0001 | 0/0 | 2406 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | ACCAA others(2401): Show |
chr19 | 48895312 | 48928372 |
| a0005c0009t0001 | 0/0 | 2394 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | ACCAA others(2389): Show |
chr19 | 48895312 | 48928372 |
| a0006c0010t0001 | 0/0 | 2406 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | ACCAA others(2401): Show |
chr19 | 48895312 | 48928372 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0001g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0001g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0001g0005 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0001g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0001g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0001g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0001g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0001g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0001g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0001g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0001g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0001g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0001g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0001g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0001g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0001g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0001g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0001g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0001g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0001g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0001g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0001g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0001g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0001g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0001g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0001g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0001g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0001g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0001g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0001g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0001g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0001g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0001g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0001g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0001g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0001g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0001g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0001g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0001g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0001g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0001g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0001g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0001g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0001g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0001g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0001g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0001g0360 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0001g0364 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0001g0366 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0001g0367 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0001g0368 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0001g0369 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0001g0375 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0001g0377 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0001g0379 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0001g0380 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0001g0381 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0001g0383 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0001g0384 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0001g0385 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0001g0386 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0001g0387 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0001g0389 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0002g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0002g0023 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0002g0025 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0002g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0002g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0002g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0002g0047 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0002g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0002g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0002g0061 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0002g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0002g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0002g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0002g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0002g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0002g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0002g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0002g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0002g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0002g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0002g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0002g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0002g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0002g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0002g0137 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0002g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0002g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0002g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0002g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0002g0147 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0002g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0002g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0002g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0002g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0002g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0002g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0002g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0002g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0002g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0002g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0002g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0002g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0002g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0002g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0002g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0002g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0002g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0002g0193 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0002g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0002g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0002g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0002g0202 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0002g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0002g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0002g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0002g0217 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0002g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0002g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0002g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0002g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0002g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0002g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0002g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0002g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0002g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0002g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0002g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0002g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0002g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0002g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0002g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0002g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0002g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0002g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0002g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0002g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0002g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0002g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0002g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0002g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0002g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0002g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0002g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0002g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0002g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0002g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0002g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0002g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0002g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0002g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0002g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0002g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0002g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0002g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0002g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0002g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0002g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0002g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0002g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0002g0349 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0002g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0002g0351 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0002g0352 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0002g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0002g0356 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0002g0361 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0002g0363 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0002g0365 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0002g0371 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0002g0372 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0002g0373 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0002g0374 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0002g0376 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0002g0388 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0003g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0003g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0003g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0003g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0003g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0003g0125 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0003g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0003g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0003g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0003g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0003g0359 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0003g0362 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0003g0370 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0003g0378 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0003g0382 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0004g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0004g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0004g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0004g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0004g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0004g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0005g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0005g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0005g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0005g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0005g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0006g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0006g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0006g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0006g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0007g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0008g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0008g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0009g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0009g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0010g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0010g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0011g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0013g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0014g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0015g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0001t0016g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0002t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0002t0002g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0002t0002g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0002t0002g0093 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0002t0002g0094 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0002t0002g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0002t0002g0097 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0002t0002g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0002t0002g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0002t0002g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0002t0002g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0002t0002g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0002t0002g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0002t0007g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0002t0007g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0003t0001g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0003t0001g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0003t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0003t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0003t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0003t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0003t0001g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0003t0001g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0003t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0003t0001g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0003t0001g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0003t0001g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0003t0001g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0003t0001g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0005t0001g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0007t0001g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0008t0012g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0001c0011t0002g0334 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0002c0004t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0002c0004t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0002c0004t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0002c0004t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0002c0004t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0002c0004t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0002c0004t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0003c0006t0007g0191 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0004c0012t0001g0337 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0005c0009t0001g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| a0006c0010t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0003 | c0006 | t0007 | g0191 | EUR | GBR | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| HG00099 | hp2 | a0001 | c0001 | t0002 | g0047 | EUR | GBR | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0200 | EUR | GBR | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| HG00140 | hp2 | a0001 | c0002 | t0002 | g0094 | EUR | GBR | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| HG00280 | hp1 | a0001 | c0001 | t0002 | g0061 | EUR | FIN | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| HG00280 | hp2 | a0001 | c0001 | t0002 | g0202 | EUR | FIN | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| HG00408 | hp1 | a0001 | c0001 | t0002 | g0069 | EAS | CHS | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0291 | EAS | CHS | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0279 | EAS | CHS | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| HG00438 | hp1 | a0001 | c0001 | t0002 | g0150 | EAS | CHS | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| HG00438 | hp2 | a0001 | c0001 | t0002 | g0170 | EAS | CHS | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0273 | EAS | CHS | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| HG00544 | hp2 | a0001 | c0001 | t0002 | g0142 | EAS | CHS | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| HG00558 | hp1 | a0001 | c0001 | t0002 | g0188 | EAS | CHS | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | CHS | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| HG00597 | hp2 | a0001 | c0001 | t0002 | g0303 | EAS | CHS | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | CHS | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0238 | EAS | CHS | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| HG00621 | hp1 | a0001 | c0001 | t0003 | g0161 | EAS | CHS | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0354 | EAS | CHS | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| HG00639 | hp1 | a0001 | c0001 | t0002 | g0216 | AMR | PUR | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0165 | AMR | PUR | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| HG00642 | hp1 | a0001 | c0001 | t0002 | g0135 | AMR | PUR | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| HG00642 | hp2 | a0001 | c0001 | t0002 | g0232 | AMR | PUR | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| HG00673 | hp1 | a0001 | c0001 | t0003 | g0204 | EAS | CHS | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| HG00673 | hp2 | a0001 | c0001 | t0002 | g0208 | EAS | CHS | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| HG00733 | hp1 | a0001 | c0001 | t0002 | g0262 | AMR | PUR | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| HG00733 | hp2 | a0001 | c0003 | t0001 | g0029 | AMR | PUR | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| HG00735 | hp1 | a0001 | c0001 | t0003 | g0030 | AMR | PUR | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| HG00735 | hp2 | a0001 | c0001 | t0002 | g0226 | AMR | PUR | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| HG00741 | hp1 | a0001 | c0001 | t0002 | g0282 | AMR | PUR | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| HG00741 | hp2 | a0001 | c0002 | t0007 | g0095 | AMR | PUR | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| HG01070 | hp1 | a0001 | c0001 | t0003 | g0063 | AMR | PUR | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0311 | AMR | PUR | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| HG01071 | hp1 | a0001 | c0001 | t0002 | g0185 | AMR | PUR | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0310 | AMR | PUR | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| HG01074 | hp1 | a0001 | c0002 | t0002 | g0099 | AMR | PUR | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0120 | AMR | PUR | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| HG01081 | hp1 | a0001 | c0001 | t0002 | g0155 | AMR | PUR | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| HG01081 | hp2 | a0001 | c0001 | t0002 | g0156 | AMR | PUR | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| HG01099 | hp1 | a0001 | c0001 | t0007 | g0285 | AMR | PUR | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| HG01099 | hp2 | a0001 | c0002 | t0001 | g0100 | AMR | PUR | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0024 | AMR | PUR | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| HG01106 | hp2 | a0001 | c0001 | t0002 | g0044 | AMR | PUR | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| HG01109 | hp1 | a0001 | c0002 | t0002 | g0101 | AMR | PUR | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| HG01109 | hp2 | a0001 | c0001 | t0002 | g0082 | AMR | PUR | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| HG01169 | hp1 | a0001 | c0002 | t0002 | g0096 | AMR | PUR | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0190 | AMR | PUR | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| HG01175 | hp1 | a0001 | c0001 | t0002 | g0199 | AMR | PUR | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| HG01175 | hp2 | a0001 | c0002 | t0002 | g0104 | AMR | PUR | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| HG01192 | hp1 | a0001 | c0002 | t0002 | g0103 | AMR | PUR | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0213 | AMR | PUR | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| HG01243 | hp1 | a0001 | c0001 | t0002 | g0115 | AMR | PUR | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| HG01243 | hp2 | a0001 | c0001 | t0009 | g0041 | AMR | PUR | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| HG01255 | hp1 | a0001 | c0001 | t0002 | g0271 | AMR | CLM | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0316 | AMR | CLM | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| HG01256 | hp1 | a0001 | c0001 | t0002 | g0278 | AMR | CLM | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| HG01256 | hp2 | a0001 | c0001 | t0002 | g0143 | AMR | CLM | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| HG01257 | hp1 | a0001 | c0001 | t0005 | g0076 | AMR | CLM | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| HG01257 | hp2 | a0001 | c0001 | t0002 | g0130 | AMR | CLM | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| HG01258 | hp1 | a0001 | c0001 | t0002 | g0276 | AMR | CLM | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| HG01258 | hp2 | a0001 | c0001 | t0002 | g0129 | AMR | CLM | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| HG01261 | hp1 | a0004 | c0012 | t0001 | g0337 | AMR | CLM | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| HG01261 | hp2 | a0001 | c0001 | t0002 | g0225 | AMR | CLM | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0263 | AMR | CLM | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0300 | AMR | CLM | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| HG01358 | hp1 | a0001 | c0002 | t0007 | g0098 | AMR | CLM | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| HG01358 | hp2 | a0001 | c0002 | t0002 | g0091 | AMR | CLM | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| HG01433 | hp1 | a0001 | c0003 | t0001 | g0296 | AMR | CLM | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| HG01433 | hp2 | a0001 | c0001 | t0002 | g0283 | AMR | CLM | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| HG01496 | hp1 | a0001 | c0001 | t0002 | g0136 | AMR | CLM | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| HG01496 | hp2 | a0001 | c0001 | t0002 | g0194 | AMR | CLM | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| HG01515 | hp1 | a0001 | c0002 | t0002 | g0093 | EUR | IBS | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0032 | EUR | IBS | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| HG01516 | hp1 | a0001 | c0001 | t0002 | g0137 | EUR | IBS | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| HG01516 | hp2 | a0001 | c0001 | t0002 | g0217 | EUR | IBS | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| HG01517 | hp1 | a0001 | c0002 | t0002 | g0097 | EUR | IBS | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| HG01517 | hp2 | a0001 | c0001 | t0002 | g0193 | EUR | IBS | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0299 | AFR | ACB | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0332 | AFR | ACB | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0046 | AFR | ACB | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| HG01891 | hp2 | a0001 | c0003 | t0001 | g0020 | AFR | ACB | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0181 | AMR | PEL | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| HG01934 | hp2 | a0001 | c0001 | t0002 | g0240 | AMR | PEL | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| HG01943 | hp1 | a0001 | c0001 | t0002 | g0052 | AMR | PEL | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| HG01943 | hp2 | a0001 | c0001 | t0002 | g0220 | AMR | PEL | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0221 | AMR | PEL | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| HG01975 | hp2 | a0001 | c0001 | t0002 | g0242 | AMR | PEL | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| HG01978 | hp2 | a0001 | c0001 | t0002 | g0222 | AMR | PEL | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0289 | AMR | PEL | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| HG01981 | hp2 | a0001 | c0001 | t0002 | g0073 | AMR | PEL | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| HG01993 | hp1 | a0001 | c0001 | t0002 | g0224 | AMR | PEL | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0381 | AMR | PEL | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| HG02004 | hp1 | a0001 | c0001 | t0002 | g0196 | AMR | PEL | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| HG02004 | hp2 | a0001 | c0001 | t0002 | g0248 | AMR | PEL | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | KHV | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | KHV | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| HG02027 | hp1 | a0001 | c0001 | t0002 | g0157 | EAS | KHV | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| HG02027 | hp2 | a0001 | c0001 | t0002 | g0237 | EAS | KHV | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| HG02040 | hp1 | a0001 | c0001 | t0003 | g0074 | EAS | KHV | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| HG02040 | hp2 | a0001 | c0001 | t0002 | g0211 | EAS | KHV | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0317 | AFR | ACB | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| HG02055 | hp2 | a0001 | c0001 | t0006 | g0304 | AFR | ACB | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| HG02056 | hp2 | a0001 | c0001 | t0002 | g0127 | EAS | KHV | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0348 | EAS | KHV | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0250 | EAS | KHV | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| HG02074 | hp2 | a0001 | c0001 | t0002 | g0132 | EAS | KHV | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | KHV | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0257 | EAS | KHV | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| HG02083 | hp1 | a0001 | c0001 | t0002 | g0126 | EAS | KHV | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| HG02083 | hp2 | a0001 | c0001 | t0002 | g0065 | EAS | KHV | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0293 | EAS | KHV | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| HG02129 | hp2 | a0001 | c0001 | t0002 | g0145 | EAS | KHV | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | KHV | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0345 | EAS | KHV | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0327 | AFR | ACB | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| HG02145 | hp2 | a0001 | c0003 | t0001 | g0295 | AFR | ACB | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| HG02148 | hp1 | a0001 | c0001 | t0005 | g0268 | AMR | PEL | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| HG02148 | hp2 | a0001 | c0001 | t0005 | g0260 | AMR | PEL | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| HG02155 | hp1 | a0001 | c0001 | t0002 | g0057 | EAS | CDX | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0341 | EAS | CDX | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0219 | EAS | CDX | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| HG02165 | hp2 | a0001 | c0001 | t0002 | g0160 | EAS | CDX | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0339 | AFR | ACB | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| HG02257 | hp2 | a0001 | c0003 | t0001 | g0001 | AFR | ACB | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0034 | AFR | ACB | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0284 | AFR | ACB | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| HG02273 | hp1 | a0001 | c0001 | t0002 | g0241 | AMR | PEL | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| HG02273 | hp2 | a0001 | c0001 | t0002 | g0261 | AMR | PEL | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0336 | AFR | ACB | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| HG02280 | hp2 | a0001 | c0001 | t0002 | g0294 | AFR | ACB | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| HG02293 | hp1 | a0001 | c0001 | t0002 | g0269 | AMR | PEL | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| HG02293 | hp2 | a0001 | c0001 | t0002 | g0265 | AMR | PEL | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| HG02300 | hp1 | a0001 | c0001 | t0002 | g0252 | AMR | PEL | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| HG02300 | hp2 | a0001 | c0001 | t0002 | g0365 | AMR | PEL | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| HG02451 | hp1 | a0001 | c0002 | t0002 | g0092 | AFR | ACB | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| HG02451 | hp2 | a0001 | c0003 | t0001 | g0001 | AFR | ACB | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0239 | EAS | KHV | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0230 | EAS | KHV | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0312 | AFR | GWD | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| HG02572 | hp2 | a0001 | c0001 | t0006 | g0080 | AFR | GWD | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0134 | SAS | PJL | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| HG02602 | hp2 | a0001 | c0002 | t0002 | g0105 | SAS | PJL | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0309 | AFR | GWD | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| HG02615 | hp2 | a0001 | c0001 | t0016 | g0338 | AFR | GWD | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0037 | AFR | GWD | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| HG02622 | hp2 | a0001 | c0001 | t0002 | g0374 | AFR | GWD | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| HG02630 | hp1 | a0001 | c0001 | t0004 | g0319 | AFR | GWD | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0306 | AFR | GWD | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| HG02647 | hp1 | a0001 | c0001 | t0010 | g0173 | AFR | GWD | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0321 | AFR | GWD | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| HG02683 | hp1 | a0001 | c0001 | t0002 | g0152 | SAS | PJL | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0206 | SAS | PJL | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| HG02698 | hp1 | a0001 | c0001 | t0002 | g0189 | SAS | PJL | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| HG02698 | hp2 | a0001 | c0001 | t0002 | g0153 | SAS | PJL | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| HG02717 | hp1 | a0002 | c0004 | t0001 | g0043 | AFR | GWD | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0048 | AFR | GWD | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| HG02723 | hp1 | a0001 | c0003 | t0001 | g0320 | AFR | GWD | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| HG02723 | hp2 | a0001 | c0001 | t0006 | g0187 | AFR | GWD | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0272 | SAS | PJL | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| HG02735 | hp2 | a0001 | c0001 | t0002 | g0124 | SAS | PJL | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| HG02738 | hp1 | a0001 | c0001 | t0002 | g0371 | SAS | PJL | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| HG02738 | hp2 | a0001 | c0011 | t0002 | g0334 | SAS | PJL | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| HG02809 | hp1 | a0001 | c0001 | t0015 | g0313 | AFR | GWD | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| HG02809 | hp2 | a0001 | c0001 | t0004 | g0331 | AFR | GWD | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| HG02818 | hp1 | a0001 | c0001 | t0003 | g0053 | AFR | GWD | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0054 | AFR | GWD | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0328 | AFR | GWD | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0167 | AFR | GWD | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0315 | AFR | GWD | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0028 | AFR | GWD | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0079 | AFR | GWD | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0308 | AFR | GWD | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0305 | AFR | GWD | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0314 | AFR | GWD | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0038 | AFR | ESN | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| HG02922 | hp2 | a0002 | c0004 | t0001 | g0026 | AFR | ESN | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| HG02965 | hp1 | a0001 | c0001 | t0013 | g0297 | AFR | ESN | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0301 | AFR | ESN | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0075 | AFR | ESN | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0027 | AFR | ESN | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| HG02976 | hp1 | a0001 | c0001 | t0009 | g0329 | AFR | ESN | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| HG02976 | hp2 | a0002 | c0004 | t0001 | g0055 | AFR | ESN | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0118 | SAS | PJL | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0183 | SAS | PJL | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| HG03041 | hp1 | a0001 | c0001 | t0014 | g0322 | AFR | GWD | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0307 | AFR | GWD | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0059 | AFR | MSL | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0383 | AFR | MSL | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0045 | AFR | ESN | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| HG03130 | hp2 | a0001 | c0003 | t0001 | g0019 | AFR | ESN | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0033 | AFR | ESN | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| HG03139 | hp2 | a0001 | c0001 | t0003 | g0323 | AFR | ESN | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0113 | AFR | ESN | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| HG03195 | hp2 | a0001 | c0003 | t0001 | g0016 | AFR | ESN | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| HG03209 | hp1 | a0001 | c0001 | t0003 | g0114 | AFR | MSL | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| HG03209 | hp2 | a0001 | c0008 | t0012 | g0014 | AFR | MSL | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0302 | AFR | MSL | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| HG03225 | hp2 | a0001 | c0003 | t0001 | g0012 | AFR | MSL | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0149 | SAS | PJL | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| HG03239 | hp2 | a0001 | c0001 | t0002 | g0148 | SAS | PJL | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| HG03453 | hp1 | a0001 | c0003 | t0001 | g0335 | AFR | MSL | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | MSL | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| HG03492 | hp1 | a0001 | c0001 | t0002 | g0259 | SAS | PJL | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| HG03492 | hp2 | a0001 | c0001 | t0002 | g0253 | SAS | PJL | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| HG03516 | hp1 | a0001 | c0003 | t0001 | g0018 | AFR | ESN | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0324 | AFR | ESN | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0042 | AFR | GWD | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| HG03540 | hp2 | a0001 | c0001 | t0004 | g0022 | AFR | GWD | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0298 | AFR | MSL | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | MSL | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| HG03669 | hp1 | a0001 | c0002 | t0002 | g0102 | SAS | PJL | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| HG03669 | hp2 | a0001 | c0007 | t0001 | g0227 | SAS | PJL | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| HG03704 | hp1 | a0001 | c0001 | t0002 | g0056 | SAS | PJL | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| HG03704 | hp2 | a0001 | c0001 | t0002 | g0243 | SAS | PJL | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| HG03710 | hp1 | a0001 | c0001 | t0002 | g0376 | SAS | PJL | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0377 | SAS | PJL | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| HG03831 | hp1 | a0001 | c0001 | t0011 | g0286 | SAS | BEB | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| HG03831 | hp2 | a0001 | c0001 | t0002 | g0349 | SAS | BEB | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0375 | SAS | BEB | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| HG03834 | hp2 | a0001 | c0001 | t0002 | g0228 | SAS | BEB | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0064 | SAS | BEB | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| HG03927 | hp2 | a0001 | c0001 | t0002 | g0116 | SAS | BEB | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0366 | SAS | BEB | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| HG03942 | hp2 | a0001 | c0001 | t0003 | g0370 | SAS | BEB | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0005 | SAS | BEB | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| HG04184 | hp2 | a0001 | c0001 | t0002 | g0372 | SAS | BEB | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0163 | SAS | STU | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| HG04199 | hp2 | a0001 | c0001 | t0002 | g0267 | SAS | STU | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| HG04204 | hp1 | a0001 | c0001 | t0003 | g0378 | SAS | STU | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| HG04204 | hp2 | a0001 | c0001 | t0002 | g0117 | SAS | STU | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| HG04228 | hp1 | a0001 | c0001 | t0002 | g0249 | SAS | STU | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0139 | SAS | STU | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0325 | AFR | YRI | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| NA18522 | hp2 | a0002 | c0004 | t0001 | g0049 | AFR | YRI | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| NA18612 | hp1 | a0001 | c0001 | t0003 | g0236 | EAS | CHB | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| NA18612 | hp2 | a0001 | c0001 | t0002 | g0123 | EAS | CHB | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0340 | EAS | CHB | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | CHB | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0106 | AFR | YRI | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| NA18906 | hp2 | a0001 | c0003 | t0001 | g0318 | AFR | YRI | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| NA18939 | hp2 | a0001 | c0001 | t0002 | g0084 | EAS | JPT | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| NA18942 | hp1 | a0001 | c0001 | t0002 | g0180 | EAS | JPT | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| NA18942 | hp2 | a0001 | c0001 | t0002 | g0254 | EAS | JPT | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0258 | EAS | JPT | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| NA18943 | hp2 | a0001 | c0001 | t0002 | g0154 | EAS | JPT | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| NA18944 | hp1 | a0001 | c0001 | t0002 | g0333 | EAS | JPT | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| NA18945 | hp1 | a0001 | c0001 | t0002 | g0373 | EAS | JPT | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0369 | EAS | JPT | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0384 | EAS | JPT | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| NA18953 | hp1 | a0001 | c0001 | t0003 | g0362 | EAS | JPT | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| NA18953 | hp2 | a0001 | c0001 | t0002 | g0179 | EAS | JPT | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| NA18956 | hp2 | a0001 | c0001 | t0003 | g0382 | EAS | JPT | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| NA18959 | hp1 | a0001 | c0001 | t0002 | g0121 | EAS | JPT | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| NA18959 | hp2 | a0001 | c0001 | t0002 | g0361 | EAS | JPT | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| NA18962 | hp1 | a0001 | c0001 | t0002 | g0388 | EAS | JPT | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0367 | EAS | JPT | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| NA18963 | hp1 | a0001 | c0005 | t0001 | g0008 | EAS | JPT | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| NA18963 | hp2 | a0001 | c0001 | t0002 | g0177 | EAS | JPT | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| NA18966 | hp2 | a0001 | c0001 | t0002 | g0068 | EAS | JPT | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| NA18968 | hp1 | a0001 | c0001 | t0002 | g0089 | EAS | JPT | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| NA18969 | hp1 | a0001 | c0001 | t0002 | g0231 | EAS | JPT | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| NA18969 | hp2 | a0001 | c0001 | t0002 | g0086 | EAS | JPT | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| NA18970 | hp1 | a0001 | c0001 | t0002 | g0070 | EAS | JPT | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| NA18971 | hp1 | a0001 | c0001 | t0002 | g0062 | EAS | JPT | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| NA18971 | hp2 | a0001 | c0001 | t0002 | g0198 | EAS | JPT | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0368 | EAS | JPT | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| NA18972 | hp2 | a0001 | c0001 | t0002 | g0288 | EAS | JPT | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0353 | EAS | JPT | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0281 | EAS | JPT | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0385 | EAS | JPT | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0379 | EAS | JPT | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0380 | EAS | JPT | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| NA18981 | hp2 | a0001 | c0001 | t0005 | g0144 | EAS | JPT | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| NA18982 | hp1 | a0001 | c0001 | t0002 | g0128 | EAS | JPT | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0342 | EAS | JPT | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| NA18983 | hp1 | a0001 | c0001 | t0002 | g0207 | EAS | JPT | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0360 | EAS | JPT | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| NA18990 | hp2 | a0001 | c0001 | t0002 | g0229 | EAS | JPT | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0364 | EAS | JPT | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| NA18992 | hp2 | a0005 | c0009 | t0001 | g0347 | EAS | JPT | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| NA18994 | hp1 | a0001 | c0001 | t0002 | g0171 | EAS | JPT | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| NA18994 | hp2 | a0001 | c0001 | t0002 | g0058 | EAS | JPT | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| NA19000 | hp1 | a0001 | c0001 | t0002 | g0209 | EAS | JPT | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0358 | EAS | JPT | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0280 | EAS | JPT | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| NA19007 | hp1 | a0001 | c0001 | t0002 | g0214 | EAS | JPT | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| NA19007 | hp2 | a0001 | c0001 | t0002 | g0233 | EAS | JPT | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0357 | EAS | JPT | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| NA19011 | hp1 | a0001 | c0001 | t0002 | g0140 | EAS | JPT | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0343 | EAS | JPT | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0277 | EAS | JPT | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0389 | EAS | JPT | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| NA19030 | hp1 | a0001 | c0001 | t0004 | g0146 | AFR | LWK | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| NA19030 | hp2 | a0001 | c0001 | t0008 | g0081 | AFR | LWK | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0050 | AFR | LWK | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0083 | AFR | LWK | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0386 | EAS | JPT | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| NA19056 | hp2 | a0001 | c0001 | t0003 | g0359 | EAS | JPT | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| NA19057 | hp1 | a0001 | c0001 | t0002 | g0110 | EAS | JPT | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| NA19060 | hp1 | a0001 | c0001 | t0002 | g0107 | EAS | JPT | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0344 | EAS | JPT | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| NA19063 | hp2 | a0001 | c0001 | t0002 | g0363 | EAS | JPT | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| NA19064 | hp1 | a0001 | c0001 | t0002 | g0244 | EAS | JPT | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| NA19065 | hp1 | a0001 | c0001 | t0002 | g0040 | EAS | JPT | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| NA19066 | hp1 | a0001 | c0001 | t0002 | g0215 | EAS | JPT | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| NA19068 | hp1 | a0001 | c0001 | t0002 | g0178 | EAS | JPT | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0387 | EAS | JPT | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| NA19070 | hp1 | a0001 | c0001 | t0002 | g0264 | EAS | JPT | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| NA19074 | hp1 | a0001 | c0001 | t0002 | g0039 | EAS | JPT | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| NA19074 | hp2 | a0001 | c0001 | t0002 | g0287 | EAS | JPT | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| NA19079 | hp1 | a0001 | c0001 | t0005 | g0182 | EAS | JPT | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| NA19081 | hp1 | a0001 | c0001 | t0002 | g0087 | EAS | JPT | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| NA19081 | hp2 | a0001 | c0001 | t0002 | g0275 | EAS | JPT | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| NA19083 | hp1 | a0001 | c0001 | t0002 | g0355 | EAS | JPT | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| NA19083 | hp2 | a0001 | c0001 | t0002 | g0175 | EAS | JPT | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| NA19084 | hp1 | a0001 | c0001 | t0002 | g0266 | EAS | JPT | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| NA19088 | hp1 | a0001 | c0005 | t0001 | g0008 | EAS | JPT | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| NA19088 | hp2 | a0001 | c0001 | t0002 | g0292 | EAS | JPT | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0346 | EAS | JPT | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| NA19091 | hp1 | a0006 | c0010 | t0001 | g0251 | EAS | JPT | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| NA19091 | hp2 | a0001 | c0001 | t0002 | g0085 | EAS | JPT | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0274 | AFR | YRI | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| NA19240 | hp2 | a0002 | c0004 | t0001 | g0235 | AFR | YRI | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| NA20129 | hp1 | a0002 | c0004 | t0001 | g0036 | AFR | ASW | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| NA20129 | hp2 | a0001 | c0001 | t0002 | g0356 | AFR | ASW | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| NA20752 | hp1 | a0001 | c0001 | t0002 | g0352 | EUR | TSI | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| NA20752 | hp2 | a0001 | c0001 | t0002 | g0351 | EUR | TSI | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| NA20805 | hp1 | a0001 | c0001 | t0002 | g0023 | EUR | TSI | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| NA20805 | hp2 | a0001 | c0001 | t0002 | g0025 | EUR | TSI | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| HG01123 | hp1 | a0001 | c0001 | t0002 | g0072 | AMR | CLM | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| HG01123 | hp2 | a0001 | c0001 | t0002 | g0172 | AMR | CLM | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0060 | AFR | ACB | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| HG02109 | hp2 | a0001 | c0001 | t0004 | g0330 | AFR | ACB | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| HG02486 | hp1 | a0002 | c0004 | t0001 | g0035 | AFR | ACB | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| HG02486 | hp2 | a0001 | c0001 | t0006 | g0078 | AFR | ACB | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| HG02559 | hp1 | a0001 | c0001 | t0002 | g0290 | AFR | ACB | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| HG02559 | hp2 | a0001 | c0001 | t0008 | g0166 | AFR | ACB | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| HG03471 | hp1 | a0001 | c0001 | t0004 | g0326 | AFR | MSL | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| HG03471 | hp2 | a0001 | c0001 | t0010 | g0021 | AFR | MSL | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | USA | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| HG06807 | hp2 | a0001 | c0001 | t0002 | g0256 | AFR | USA | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| NA18955 | hp1 | a0001 | c0001 | t0002 | g0350 | EAS | JPT | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| NA20300 | hp1 | a0001 | c0003 | t0001 | g0051 | AFR | USA | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| NA20300 | hp2 | a0001 | c0001 | t0002 | g0017 | AFR | USA | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| NA21309 | hp1 | a0001 | c0001 | t0002 | g0077 | AFR | LWK | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| NA21309 | hp2 | a0001 | c0003 | t0001 | g0013 | AFR | LWK | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0002 | g0147 | REF | REF | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0003 | g0125 | REF | REF | NUCB1_chr19_48895312_48928372 | NUCB1 | chr19 | 48895312 | 48928372 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:48904438 | A | G | 1 | a0004 | 1 | HG01261.hp1 | missense_variant | MODERATE | c.227A>G | p.Asn76Ser | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 3/13 | 299/2406 | 227/1386 | 76/461 | chr19 | 48904438 | |||
| chr19:48905769 | G | A | 1 | a0003 | 1 | HG00099.hp1 | missense_variant | MODERATE | c.260G>A | p.Arg87Gln | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 4/13 | 332/2406 | 260/1386 | 87/461 | chr19 | 48905769 | |||
| chr19:48913164 | C | T | 1 | a0006 | 1 | NA19091.hp1 | missense_variant | MODERATE | c.634C>T | p.Arg212Trp | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 6/13 | 706/2406 | 634/1386 | 212/461 | chr19 | 48913164 | |||
| chr19:48918759 | A | C | 1 | a0005 | 1 | NA18992.hp2 | missense_variant | MODERATE | c.791A>C | p.Glu264Ala | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 8/13 | 863/2406 | 791/1386 | 264/461 | chr19 | 48918759 | |||
| chr19:48919268 | C | A | 1 | a0005 | 1 | NA18992.hp2 | missense_variant | MODERATE | c.984C>A | p.Asp328Glu | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 10/13 | 1056/2406 | 984/1386 | 328/461 | chr19 | 48919268 | |||
| chr19:48919269 | A | C | 1 | a0005 | 1 | NA18992.hp2 | missense_variant | MODERATE | c.985A>C | p.Thr329Pro | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 10/13 | 1057/2406 | 985/1386 | 329/461 | chr19 | 48919269 | |||
| chr19:48919270 | C | A | 1 | a0005 | 1 | NA18992.hp2 | missense_variant | MODERATE | c.986C>A | p.Thr329Asn | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 10/13 | 1058/2406 | 986/1386 | 329/461 | chr19 | 48919270 | |||
| chr19:48921163 | A | G | 1 | a0002 | 7 | HG02486.hp1 HG02717.hp1 HG02922.hp2 others(4): Show |
missense_variant | MODERATE | c.1012A>G | p.Met338Val | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 11/13 | 1084/2406 | 1012/1386 | 338/461 | chr19 | 48921163 | |||
| chr19:48921290 | GCCGCCTG others(5): Show |
G | 1 | a0005 | 1 | NA18992.hp2 | disruptive_inframe_deletion | MODERATE | c.1142_1153delGCCTGG others(6): Show |
p.Arg381_Ala384del | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 11/13 | 1214/2406 | 1142/1386 | 381/461 | INFO_REALIGN_3_PRIME | chr19 | 48921290 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:48904403 | G | A | 1 | a0001c0002 | 15 | HG00140.hp2 HG00741.hp2 HG01074.hp1 others(12): Show |
synonymous_variant | LOW | c.192G>A | p.Thr64Thr | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 3/13 | 264/2406 | 192/1386 | 64/461 | chr19 | 48904403 | |||
| chr19:48913085 | C | T | 1 | a0001c0011 | 1 | HG02738.hp2 | synonymous_variant | LOW | c.555C>T | p.His185His | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 6/13 | 627/2406 | 555/1386 | 185/461 | chr19 | 48913085 | |||
| chr19:48913136 | G | A | 1 | a0001c0007 | 1 | HG03669.hp2 | synonymous_variant | LOW | c.606G>A | p.Ala202Ala | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 6/13 | 678/2406 | 606/1386 | 202/461 | chr19 | 48913136 | |||
| chr19:48921177 | C | T | 1 | a0001c0005 | 2 | NA18963.hp1 NA19088.hp1 |
synonymous_variant | LOW | c.1026C>T | p.Tyr342Tyr | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 11/13 | 1098/2406 | 1026/1386 | 342/461 | chr19 | 48921177 | |||
| chr19:48922319 | C | T | 1 | a0001c0003 | 15 | HG00733.hp2 HG01433.hp1 HG01891.hp2 others(12): Show |
splice_region_variant&synonymous_variant | LOW | c.1281C>T | p.Asp427Asp | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 13/13 | 1353/2406 | 1281/1386 | 427/461 | chr19 | 48922319 | |||
| chr19:48922394 | C | G | 1 | a0001c0008 | 1 | HG03209.hp2 | synonymous_variant | LOW | c.1356C>G | p.Leu452Leu | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 13/13 | 1428/2406 | 1356/1386 | 452/461 | chr19 | 48922394 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:48922515 | T | C | 26 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(23): Show |
380 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(377): Show |
3_prime_UTR_variant | MODIFIER | c.*91T>C | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 13/13 | 91 | chr19 | 48922515 | ||||||
| chr19:48922563 | G | A | 1 | a0001c0001t0008 | 2 | HG02559.hp2 NA19030.hp2 |
3_prime_UTR_variant | MODIFIER | c.*139G>A | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 13/13 | 139 | chr19 | 48922563 | ||||||
| chr19:48922581 | G | A | 4 | a0001c0001t0002 a0001c0001t0011 a0001c0002t0002 others(1): Show |
153 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(150): Show |
3_prime_UTR_variant | MODIFIER | c.*157G>A | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 13/13 | 157 | chr19 | 48922581 | ||||||
| chr19:48922703 | G | A | 1 | a0001c0001t0011 | 1 | HG03831.hp1 | 3_prime_UTR_variant | MODIFIER | c.*279G>A | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 13/13 | 279 | chr19 | 48922703 | ||||||
| chr19:48922708 | C | T | 1 | a0001c0001t0016 | 1 | HG02615.hp2 | 3_prime_UTR_variant | MODIFIER | c.*284C>T | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 13/13 | 284 | chr19 | 48922708 | ||||||
| chr19:48922765 | T | C | 4 | a0001c0001t0004 a0001c0001t0006 a0001c0001t0010 others(1): Show |
13 | HG02055.hp2 HG02109.hp2 HG02486.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*341T>C | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 13/13 | 341 | chr19 | 48922765 | ||||||
| chr19:48922808 | T | G | 1 | a0001c0001t0008 | 2 | HG02559.hp2 NA19030.hp2 |
3_prime_UTR_variant | MODIFIER | c.*384T>G | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 13/13 | 384 | chr19 | 48922808 | ||||||
| chr19:48922823 | G | T | 1 | a0001c0001t0009 | 2 | HG01243.hp2 HG02976.hp1 |
3_prime_UTR_variant | MODIFIER | c.*399G>T | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 13/13 | 399 | chr19 | 48922823 | ||||||
| chr19:48922842 | G | A | 4 | a0001c0001t0002 a0001c0001t0011 a0001c0002t0002 others(1): Show |
153 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(150): Show |
3_prime_UTR_variant | MODIFIER | c.*418G>A | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 13/13 | 418 | chr19 | 48922842 | ||||||
| chr19:48923092 | C | G | 1 | a0001c0001t0015 | 1 | HG02809.hp1 | 3_prime_UTR_variant | MODIFIER | c.*668C>G | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 13/13 | 668 | chr19 | 48923092 | ||||||
| chr19:48923139 | C | G | 1 | a0001c0001t0005 | 5 | HG01257.hp1 HG02148.hp1 HG02148.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*715C>G | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 13/13 | 715 | chr19 | 48923139 | ||||||
| chr19:48923209 | C | T | 1 | a0001c0001t0014 | 1 | HG03041.hp1 | 3_prime_UTR_variant | MODIFIER | c.*785C>T | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 13/13 | 785 | chr19 | 48923209 | ||||||
| chr19:48923210 | G | A | 1 | a0001c0001t0006 | 4 | HG02055.hp2 HG02486.hp2 HG02572.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*786G>A | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 13/13 | 786 | chr19 | 48923210 | ||||||
| chr19:48923230 | T | C | 1 | a0001c0008t0012 | 1 | HG03209.hp2 | 3_prime_UTR_variant | MODIFIER | c.*806T>C | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 13/13 | 806 | chr19 | 48923230 | ||||||
| chr19:48923231 | T | C | 3 | a0001c0001t0007 a0001c0002t0007 a0003c0006t0007 |
4 | HG00099.hp1 HG00741.hp2 HG01099.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*807T>C | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 13/13 | 807 | chr19 | 48923231 | ||||||
| chr19:48923241 | G | A | 1 | a0001c0008t0012 | 1 | HG03209.hp2 | 3_prime_UTR_variant | MODIFIER | c.*817G>A | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 13/13 | 817 | chr19 | 48923241 | ||||||
| chr19:48923289 | G | A | 1 | a0001c0001t0013 | 1 | HG02965.hp1 | 3_prime_UTR_variant | MODIFIER | c.*865G>A | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 13/13 | 865 | chr19 | 48923289 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:48900420 | G | C | 82 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(79): Show |
84 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(81): Show |
intron_variant | MODIFIER | c.-12+48G>C | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 1/12 | chr19 | 48900420 | |||||||
| chr19:48900617 | C | T | 3 | a0001c0001t0001g0387 a0001c0001t0001g0389 a0001c0001t0002g0388 |
3 | NA18962.hp1 NA19012.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.-11-169C>T | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 1/12 | chr19 | 48900617 | |||||||
| chr19:48900731 | G | A | 1 | a0001c0001t0001g0090 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.-11-55G>A | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 1/12 | chr19 | 48900731 | |||||||
| chr19:48900765 | C | G | 3 | a0001c0001t0001g0384 a0001c0001t0001g0385 a0001c0001t0001g0386 |
3 | NA18950.hp2 NA18977.hp1 NA19054.hp2 |
intron_variant | MODIFIER | c.-11-21C>G | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 1/12 | chr19 | 48900765 | |||||||
| chr19:48900956 | A | G | 1 | a0001c0001t0001g0383 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.135+25A>G | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 2/12 | chr19 | 48900956 | |||||||
| chr19:48901011 | G | T | 1 | a0001c0001t0003g0382 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.135+80G>T | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 2/12 | chr19 | 48901011 | |||||||
| chr19:48901110 | CCTGACT | C | 45 | a0001c0001t0001g0009 a0001c0001t0001g0090 a0001c0001t0001g0340 others(42): Show |
47 | HG00621.hp2 HG01993.hp2 HG02071.hp1 others(44): Show |
intron_variant | MODIFIER | c.135+184_135+189del others(6): Show |
NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr19 | 48901110 | ||||||
| chr19:48901136 | C | T | 82 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(79): Show |
84 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(81): Show |
intron_variant | MODIFIER | c.135+205C>T | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 2/12 | chr19 | 48901136 | |||||||
| chr19:48901191 | A | T | 3 | a0001c0001t0001g0339 a0001c0001t0016g0338 a0004c0012t0001g0337 |
3 | HG01261.hp1 HG02257.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.135+260A>T | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 2/12 | chr19 | 48901191 | |||||||
| chr19:48901278 | T | G | 16 | a0001c0001t0001g0106 a0001c0002t0001g0100 a0001c0002t0002g0091 others(13): Show |
16 | HG00140.hp2 HG00741.hp2 HG01074.hp1 others(13): Show |
intron_variant | MODIFIER | c.135+347T>G | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 2/12 | chr19 | 48901278 | |||||||
| chr19:48901327 | C | T | 3 | a0001c0001t0001g0336 a0001c0003t0001g0335 a0001c0011t0002g0334 |
3 | HG02280.hp1 HG02738.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.135+396C>T | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 2/12 | chr19 | 48901327 | |||||||
| chr19:48901958 | C | T | 1 | a0001c0001t0001g0106 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.135+1027C>T | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 2/12 | chr19 | 48901958 | |||||||
| chr19:48902255 | C | T | 1 | a0001c0001t0002g0333 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.135+1324C>T | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 2/12 | chr19 | 48902255 | |||||||
| chr19:48902311 | A | G | 25 | a0001c0001t0001g0309 a0001c0001t0001g0310 a0001c0001t0001g0311 others(22): Show |
25 | HG01070.hp2 HG01071.hp2 HG01255.hp2 others(22): Show |
intron_variant | MODIFIER | c.135+1380A>G | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 2/12 | chr19 | 48902311 | |||||||
| chr19:48902412 | TCCTTTTT others(1): Show |
T | 24 | a0001c0001t0001g0309 a0001c0001t0001g0310 a0001c0001t0001g0311 others(21): Show |
24 | HG01070.hp2 HG01071.hp2 HG01255.hp2 others(21): Show |
intron_variant | MODIFIER | c.135+1482_135+1489d others(10): Show |
NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 2/12 | chr19 | 48902412 | |||||||
| chr19:48902413 | C | T | 95 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(92): Show |
97 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(94): Show |
intron_variant | MODIFIER | c.135+1482C>T | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 2/12 | chr19 | 48902413 | |||||||
| chr19:48902420 | CT | C | 95 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(92): Show |
97 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(94): Show |
intron_variant | MODIFIER | c.135+1507delT | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr19 | 48902420 | ||||||
| chr19:48902420 | CTT | C | 19 | a0001c0001t0001g0028 a0001c0001t0001g0106 a0001c0001t0002g0052 others(16): Show |
19 | HG00140.hp2 HG00741.hp2 HG01074.hp1 others(16): Show |
intron_variant | MODIFIER | c.135+1506_135+1507d others(4): Show |
NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr19 | 48902420 | ||||||
| chr19:48902422 | T | C | 24 | a0001c0001t0001g0309 a0001c0001t0001g0310 a0001c0001t0001g0311 others(21): Show |
24 | HG01070.hp2 HG01071.hp2 HG01255.hp2 others(21): Show |
intron_variant | MODIFIER | c.135+1491T>C | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 2/12 | chr19 | 48902422 | |||||||
| chr19:48902423 | T | C | 1 | a0001c0001t0001g0332 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.135+1492T>C | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 2/12 | chr19 | 48902423 | |||||||
| chr19:48902425 | T | C | 6 | a0001c0001t0001g0108 a0001c0001t0001g0109 a0001c0001t0001g0111 others(3): Show |
6 | NA18955.hp2 NA18960.hp2 NA18980.hp1 others(3): Show |
intron_variant | MODIFIER | c.135+1494T>C | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 2/12 | chr19 | 48902425 | |||||||
| chr19:48902438 | T | G | 120 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(117): Show |
122 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(119): Show |
intron_variant | MODIFIER | c.135+1507T>G | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 2/12 | chr19 | 48902438 | |||||||
| chr19:48902478 | A | G | 1 | a0001c0001t0004g0331 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.135+1547A>G | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 2/12 | chr19 | 48902478 | |||||||
| chr19:48902768 | C | T | 1 | a0001c0001t0004g0330 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.136-1579C>T | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 2/12 | chr19 | 48902768 | |||||||
| chr19:48902879 | G | C | 25 | a0001c0001t0001g0309 a0001c0001t0001g0310 a0001c0001t0001g0311 others(22): Show |
25 | HG01070.hp2 HG01071.hp2 HG01255.hp2 others(22): Show |
intron_variant | MODIFIER | c.136-1468G>C | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 2/12 | chr19 | 48902879 | |||||||
| chr19:48902918 | A | T | 120 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(117): Show |
122 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(119): Show |
intron_variant | MODIFIER | c.136-1429A>T | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 2/12 | chr19 | 48902918 | |||||||
| chr19:48902937 | G | GTA | 26 | a0001c0001t0001g0083 a0001c0001t0001g0106 a0001c0001t0001g0312 others(23): Show |
26 | HG01243.hp1 HG01255.hp2 HG01884.hp2 others(23): Show |
intron_variant | MODIFIER | c.136-1394_136-1393d others(4): Show |
NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr19 | 48902937 | ||||||
| chr19:48902937 | G | GTATA | 97 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0024 others(94): Show |
99 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(96): Show |
intron_variant | MODIFIER | c.136-1396_136-1393d others(6): Show |
NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr19 | 48902937 | ||||||
| chr19:48902937 | G | GTATATA | 33 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0015 others(30): Show |
35 | HG00621.hp2 HG01891.hp2 HG02257.hp2 others(32): Show |
intron_variant | MODIFIER | c.136-1398_136-1393d others(8): Show |
NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr19 | 48902937 | ||||||
| chr19:48902937 | G | GTATATAT others(1): Show |
12 | a0001c0001t0001g0090 a0001c0001t0001g0340 a0001c0001t0001g0341 others(9): Show |
12 | HG02071.hp1 HG02132.hp2 HG02155.hp2 others(9): Show |
intron_variant | MODIFIER | c.136-1400_136-1393d others(10): Show |
NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr19 | 48902937 | ||||||
| chr19:48902956 | T | C | 50 | a0001c0001t0001g0009 a0001c0001t0001g0090 a0001c0001t0001g0113 others(47): Show |
52 | HG00621.hp2 HG01993.hp2 HG02071.hp1 others(49): Show |
intron_variant | MODIFIER | c.136-1391T>C | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 2/12 | chr19 | 48902956 | |||||||
| chr19:48903376 | G | GGTGTAGA others(10): Show |
1 | a0001c0002t0002g0105 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.136-970_136-969ins others(17): Show |
NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr19 | 48903376 | ||||||
| chr19:48903380 | A | AGATGGAT others(9): Show |
15 | a0001c0001t0001g0106 a0001c0002t0001g0100 a0001c0002t0002g0091 others(12): Show |
15 | HG00140.hp2 HG00741.hp2 HG01074.hp1 others(12): Show |
intron_variant | MODIFIER | c.136-954_136-953ins others(16): Show |
NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr19 | 48903380 | ||||||
| chr19:48903380 | A | G | 1 | a0001c0002t0002g0105 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.136-967A>G | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 2/12 | chr19 | 48903380 | |||||||
| chr19:48903392 | A | AGGTGGAT others(9): Show |
104 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(101): Show |
106 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(103): Show |
intron_variant | MODIFIER | c.136-954_136-953ins others(16): Show |
NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr19 | 48903392 | ||||||
| chr19:48903394 | T | G | 120 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(117): Show |
122 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(119): Show |
intron_variant | MODIFIER | c.136-953T>G | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 2/12 | chr19 | 48903394 | |||||||
| chr19:48903408 | G | A | 1 | a0001c0001t0003g0370 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.136-939G>A | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 2/12 | chr19 | 48903408 | |||||||
| chr19:48903450 | A | G | 75 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(72): Show |
77 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(74): Show |
intron_variant | MODIFIER | c.136-897A>G | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 2/12 | chr19 | 48903450 | |||||||
| chr19:48903454 | G | A | 16 | a0001c0001t0001g0106 a0001c0002t0001g0100 a0001c0002t0002g0091 others(13): Show |
16 | HG00140.hp2 HG00741.hp2 HG01074.hp1 others(13): Show |
intron_variant | MODIFIER | c.136-893G>A | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 2/12 | chr19 | 48903454 | |||||||
| chr19:48903458 | T | TTGGATGG others(9): Show |
1 | a0001c0001t0002g0107 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.136-860_136-845dup others(16): Show |
NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr19 | 48903458 | ||||||
| chr19:48903471 | C | T | 16 | a0001c0001t0001g0106 a0001c0002t0001g0100 a0001c0002t0002g0091 others(13): Show |
16 | HG00140.hp2 HG00741.hp2 HG01074.hp1 others(13): Show |
intron_variant | MODIFIER | c.136-876C>T | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 2/12 | chr19 | 48903471 | |||||||
| chr19:48903474 | G | T | 16 | a0001c0001t0001g0106 a0001c0002t0001g0100 a0001c0002t0002g0091 others(13): Show |
16 | HG00140.hp2 HG00741.hp2 HG01074.hp1 others(13): Show |
intron_variant | MODIFIER | c.136-873G>T | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 2/12 | chr19 | 48903474 | |||||||
| chr19:48903524 | G | GGATGGGT others(13): Show |
1 | a0001c0001t0002g0117 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.136-803_136-784dup others(20): Show |
NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr19 | 48903524 | ||||||
| chr19:48903533 | G | T | 1 | a0001c0001t0002g0082 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.136-814G>T | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 2/12 | chr19 | 48903533 | |||||||
| chr19:48903544 | C | G | 16 | a0001c0001t0001g0106 a0001c0002t0001g0100 a0001c0002t0002g0091 others(13): Show |
16 | HG00140.hp2 HG00741.hp2 HG01074.hp1 others(13): Show |
intron_variant | MODIFIER | c.136-803C>G | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 2/12 | chr19 | 48903544 | |||||||
| chr19:48903569 | A | G | 3 | a0001c0001t0001g0309 a0001c0001t0001g0310 a0001c0001t0001g0311 |
3 | HG01070.hp2 HG01071.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.136-778A>G | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 2/12 | chr19 | 48903569 | |||||||
| chr19:48903590 | A | G | 1 | a0001c0001t0001g0369 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.136-757A>G | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 2/12 | chr19 | 48903590 | |||||||
| chr19:48903647 | C | A | 76 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(73): Show |
78 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(75): Show |
intron_variant | MODIFIER | c.136-700C>A | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 2/12 | chr19 | 48903647 | |||||||
| chr19:48903673 | AGTGGATG others(13): Show |
A | 76 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(73): Show |
78 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(75): Show |
intron_variant | MODIFIER | c.136-638_136-619del others(20): Show |
NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr19 | 48903673 | ||||||
| chr19:48903718 | A | G | 52 | a0001c0001t0001g0009 a0001c0001t0001g0090 a0001c0001t0001g0113 others(49): Show |
54 | HG00621.hp2 HG01993.hp2 HG02055.hp2 others(51): Show |
intron_variant | MODIFIER | c.136-629A>G | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 2/12 | chr19 | 48903718 | |||||||
| chr19:48903828 | A | G | 1 | a0001c0001t0002g0303 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.136-519A>G | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 2/12 | chr19 | 48903828 | |||||||
| chr19:48903858 | GTGGA | G | 175 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(172): Show |
179 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(176): Show |
intron_variant | MODIFIER | c.136-465_136-462del others(4): Show |
NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr19 | 48903858 | ||||||
| chr19:48903858 | GTGGATGG others(1): Show |
G | 78 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(75): Show |
80 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(77): Show |
intron_variant | MODIFIER | c.136-469_136-462del others(8): Show |
NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr19 | 48903858 | ||||||
| chr19:48903882 | A | ATGGG | 75 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(72): Show |
77 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(74): Show |
intron_variant | MODIFIER | c.136-457_136-454dup others(4): Show |
NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr19 | 48903882 | ||||||
| chr19:48903882 | A | G | 105 | a0001c0001t0001g0009 a0001c0001t0001g0054 a0001c0001t0001g0090 others(102): Show |
107 | HG00140.hp2 HG00621.hp2 HG00741.hp2 others(104): Show |
intron_variant | MODIFIER | c.136-465A>G | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 2/12 | chr19 | 48903882 | |||||||
| chr19:48903894 | A | G | 3 | a0001c0001t0001g0300 a0001c0001t0001g0301 a0001c0001t0001g0302 |
3 | HG01346.hp2 HG02965.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.136-453A>G | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 2/12 | chr19 | 48903894 | |||||||
| chr19:48903956 | GGATGGGT others(16): Show |
G | 3 | a0001c0001t0001g0300 a0001c0001t0001g0301 a0001c0001t0001g0302 |
3 | HG01346.hp2 HG02965.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.136-379_136-357del others(23): Show |
NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr19 | 48903956 | ||||||
| chr19:48903966 | A | G | 1 | a0001c0001t0002g0199 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.136-381A>G | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 2/12 | chr19 | 48903966 | |||||||
| chr19:48903982 | T | C | 55 | a0001c0001t0001g0009 a0001c0001t0001g0090 a0001c0001t0001g0113 others(52): Show |
57 | HG00621.hp2 HG01993.hp2 HG02055.hp2 others(54): Show |
intron_variant | MODIFIER | c.136-365T>C | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 2/12 | chr19 | 48903982 | |||||||
| chr19:48903987 | G | GGATA | 4 | a0001c0001t0001g0312 a0001c0001t0001g0314 a0001c0001t0001g0315 others(1): Show |
4 | HG02572.hp1 HG02809.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.136-356_136-353dup others(4): Show |
NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr19 | 48903987 | ||||||
| chr19:48904102 | G | A | 1 | a0001c0001t0002g0143 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.136-245G>A | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 2/12 | chr19 | 48904102 | |||||||
| chr19:48904111 | A | C | 1 | a0001c0001t0002g0294 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.136-236A>C | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 2/12 | chr19 | 48904111 | |||||||
| chr19:48904148 | T | C | 1 | a0001c0001t0004g0022 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.136-199T>C | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 2/12 | chr19 | 48904148 | |||||||
| chr19:48904458 | C | T | 15 | a0001c0002t0001g0100 a0001c0002t0002g0091 a0001c0002t0002g0092 others(12): Show |
15 | HG00140.hp2 HG00741.hp2 HG01074.hp1 others(12): Show |
splice_region_variant&intron_variant | LOW | c.243+4C>T | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 3/12 | chr19 | 48904458 | |||||||
| chr19:48904476 | C | T | 16 | a0001c0001t0001g0106 a0001c0002t0001g0100 a0001c0002t0002g0091 others(13): Show |
16 | HG00140.hp2 HG00741.hp2 HG01074.hp1 others(13): Show |
intron_variant | MODIFIER | c.243+22C>T | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 3/12 | chr19 | 48904476 | |||||||
| chr19:48904490 | C | T | 1 | a0001c0001t0001g0293 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.243+36C>T | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 3/12 | chr19 | 48904490 | |||||||
| chr19:48904522 | G | A | 1 | a0001c0001t0001g0316 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.243+68G>A | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 3/12 | chr19 | 48904522 | |||||||
| chr19:48904527 | C | CT | 36 | a0001c0001t0001g0079 a0001c0001t0001g0300 a0001c0001t0001g0301 others(33): Show |
36 | HG01070.hp2 HG01071.hp2 HG01255.hp2 others(33): Show |
intron_variant | MODIFIER | c.243+88dupT | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr19 | 48904527 | ||||||
| chr19:48904587 | C | T | 2 | a0001c0001t0001g0314 a0001c0001t0001g0315 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.243+133C>T | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 3/12 | chr19 | 48904587 | |||||||
| chr19:48904669 | G | A | 1 | a0001c0001t0005g0144 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.243+215G>A | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 3/12 | chr19 | 48904669 | |||||||
| chr19:48904690 | A | G | 16 | a0001c0001t0001g0106 a0001c0002t0001g0100 a0001c0002t0002g0091 others(13): Show |
16 | HG00140.hp2 HG00741.hp2 HG01074.hp1 others(13): Show |
intron_variant | MODIFIER | c.243+236A>G | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 3/12 | chr19 | 48904690 | |||||||
| chr19:48904758 | G | A | 76 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(73): Show |
78 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(75): Show |
intron_variant | MODIFIER | c.243+304G>A | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 3/12 | chr19 | 48904758 | |||||||
| chr19:48904765 | T | G | 183 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(180): Show |
187 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(184): Show |
intron_variant | MODIFIER | c.243+311T>G | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 3/12 | chr19 | 48904765 | |||||||
| chr19:48904972 | TG | T | 76 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(73): Show |
78 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(75): Show |
intron_variant | MODIFIER | c.243+521delG | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr19 | 48904972 | ||||||
| chr19:48904988 | C | T | 5 | a0001c0001t0001g0298 a0001c0001t0001g0299 a0001c0001t0013g0297 others(2): Show |
5 | HG01433.hp1 HG01884.hp1 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.243+534C>T | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 3/12 | chr19 | 48904988 | |||||||
| chr19:48905046 | C | T | 357 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(354): Show |
365 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(362): Show |
intron_variant | MODIFIER | c.243+592C>T | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 3/12 | chr19 | 48905046 | |||||||
| chr19:48905101 | C | G | 16 | a0001c0001t0001g0106 a0001c0002t0001g0100 a0001c0002t0002g0091 others(13): Show |
16 | HG00140.hp2 HG00741.hp2 HG01074.hp1 others(13): Show |
intron_variant | MODIFIER | c.243+647C>G | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 3/12 | chr19 | 48905101 | |||||||
| chr19:48905144 | G | C | 2 | a0001c0001t0001g0024 a0001c0001t0002g0023 |
2 | HG01106.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.244-609G>C | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 3/12 | chr19 | 48905144 | |||||||
| chr19:48905410 | G | A | 1 | a0001c0001t0001g0118 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.244-343G>A | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 3/12 | chr19 | 48905410 | |||||||
| chr19:48905642 | A | G | 1 | a0001c0001t0005g0076 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.244-111A>G | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 3/12 | chr19 | 48905642 | |||||||
| chr19:48905686 | T | C | 15 | a0001c0002t0001g0100 a0001c0002t0002g0091 a0001c0002t0002g0092 others(12): Show |
15 | HG00140.hp2 HG00741.hp2 HG01074.hp1 others(12): Show |
intron_variant | MODIFIER | c.244-67T>C | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 3/12 | chr19 | 48905686 | |||||||
| chr19:48905747 | T | C | 16 | a0001c0001t0001g0106 a0001c0002t0001g0100 a0001c0002t0002g0091 others(13): Show |
16 | HG00140.hp2 HG00741.hp2 HG01074.hp1 others(13): Show |
splice_region_variant&intron_variant | LOW | c.244-6T>C | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 3/12 | chr19 | 48905747 | |||||||
| chr19:48905940 | TCACTC | T | 79 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(76): Show |
81 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(78): Show |
intron_variant | MODIFIER | c.376+57_376+61delAC others(3): Show |
NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr19 | 48905940 | ||||||
| chr19:48905964 | TGTGCTAG others(4): Show |
T | 79 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(76): Show |
81 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(78): Show |
intron_variant | MODIFIER | c.376+83_376+93delCT others(9): Show |
NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr19 | 48905964 | ||||||
| chr19:48905994 | C | T | 1 | a0001c0001t0001g0291 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.376+109C>T | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 4/12 | chr19 | 48905994 | |||||||
| chr19:48906017 | G | A | 3 | a0001c0001t0001g0339 a0001c0001t0016g0338 a0004c0012t0001g0337 |
3 | HG01261.hp1 HG02257.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.376+132G>A | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 4/12 | chr19 | 48906017 | |||||||
| chr19:48906175 | G | T | 1 | a0001c0001t0002g0290 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.376+290G>T | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 4/12 | chr19 | 48906175 | |||||||
| chr19:48906196 | G | A | 3 | a0001c0001t0001g0300 a0001c0001t0001g0301 a0001c0001t0001g0302 |
3 | HG01346.hp2 HG02965.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.376+311G>A | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 4/12 | chr19 | 48906196 | |||||||
| chr19:48906211 | T | C | 160 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(157): Show |
164 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(161): Show |
intron_variant | MODIFIER | c.376+326T>C | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 4/12 | chr19 | 48906211 | |||||||
| chr19:48906368 | C | T | 1 | a0001c0001t0001g0075 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.376+483C>T | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 4/12 | chr19 | 48906368 | |||||||
| chr19:48906390 | T | G | 1 | a0001c0001t0002g0145 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.376+505T>G | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 4/12 | chr19 | 48906390 | |||||||
| chr19:48906403 | C | CA | 12 | a0001c0001t0001g0119 a0001c0001t0001g0120 a0001c0001t0001g0149 others(9): Show |
12 | HG00438.hp1 HG01074.hp2 HG02040.hp1 others(9): Show |
intron_variant | MODIFIER | c.376+536dupA | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr19 | 48906403 | ||||||
| chr19:48906403 | C | CAA | 148 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(145): Show |
152 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(149): Show |
intron_variant | MODIFIER | c.376+535_376+536dup others(2): Show |
NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr19 | 48906403 | ||||||
| chr19:48906403 | C | CAAA | 9 | a0001c0001t0001g0090 a0001c0001t0001g0113 a0001c0001t0001g0339 others(6): Show |
9 | HG01261.hp1 HG02055.hp2 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.376+534_376+536dup others(3): Show |
NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr19 | 48906403 | ||||||
| chr19:48906535 | A | G | 1 | a0001c0001t0002g0142 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.376+650A>G | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 4/12 | chr19 | 48906535 | |||||||
| chr19:48906929 | C | T | 1 | a0001c0001t0001g0106 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.376+1044C>T | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 4/12 | chr19 | 48906929 | |||||||
| chr19:48906934 | G | T | 121 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(118): Show |
123 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(120): Show |
intron_variant | MODIFIER | c.376+1049G>T | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 4/12 | chr19 | 48906934 | |||||||
| chr19:48906950 | C | G | 4 | a0001c0001t0001g0366 a0001c0001t0001g0381 a0001c0001t0002g0349 others(1): Show |
4 | HG01993.hp2 HG02300.hp2 HG03831.hp2 others(1): Show |
intron_variant | MODIFIER | c.376+1065C>G | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 4/12 | chr19 | 48906950 | |||||||
| chr19:48906979 | C | CT | 157 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(154): Show |
161 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(158): Show |
intron_variant | MODIFIER | c.376+1107dupT | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr19 | 48906979 | ||||||
| chr19:48906998 | A | G | 2 | a0001c0001t0001g0310 a0001c0001t0001g0311 |
2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.376+1113A>G | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 4/12 | chr19 | 48906998 | |||||||
| chr19:48907005 | C | T | 2 | a0001c0001t0002g0072 a0001c0001t0002g0073 |
2 | HG01123.hp1 HG01981.hp2 |
intron_variant | MODIFIER | c.376+1120C>T | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 4/12 | chr19 | 48907005 | |||||||
| chr19:48907040 | T | C | 55 | a0001c0001t0001g0009 a0001c0001t0001g0090 a0001c0001t0001g0113 others(52): Show |
57 | HG00621.hp2 HG01993.hp2 HG02055.hp2 others(54): Show |
intron_variant | MODIFIER | c.376+1155T>C | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 4/12 | chr19 | 48907040 | |||||||
| chr19:48907216 | G | T | 39 | a0001c0001t0001g0106 a0001c0001t0001g0309 a0001c0001t0001g0310 others(36): Show |
39 | HG00140.hp2 HG00741.hp2 HG01070.hp2 others(36): Show |
intron_variant | MODIFIER | c.376+1331G>T | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 4/12 | chr19 | 48907216 | |||||||
| chr19:48907272 | C | CT | 30 | a0001c0001t0001g0007 a0001c0001t0001g0071 a0001c0001t0001g0112 others(27): Show |
31 | HG00741.hp1 HG01099.hp1 HG01175.hp2 others(28): Show |
intron_variant | MODIFIER | c.376+1405dupT | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr19 | 48907272 | ||||||
| chr19:48907289 | T | C | 1 | a0001c0001t0002g0025 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.376+1404T>C | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 4/12 | chr19 | 48907289 | |||||||
| chr19:48907338 | C | T | 55 | a0001c0001t0001g0009 a0001c0001t0001g0090 a0001c0001t0001g0113 others(52): Show |
57 | HG00621.hp2 HG01993.hp2 HG02055.hp2 others(54): Show |
intron_variant | MODIFIER | c.376+1453C>T | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 4/12 | chr19 | 48907338 | |||||||
| chr19:48907417 | A | G | 1 | a0001c0003t0001g0020 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.376+1532A>G | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 4/12 | chr19 | 48907417 | |||||||
| chr19:48907615 | C | T | 1 | a0001c0001t0001g0280 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.376+1730C>T | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 4/12 | chr19 | 48907615 | |||||||
| chr19:48907663 | G | A | 76 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(73): Show |
78 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(75): Show |
intron_variant | MODIFIER | c.376+1778G>A | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 4/12 | chr19 | 48907663 | |||||||
| chr19:48907713 | T | C | 181 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(178): Show |
185 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(182): Show |
intron_variant | MODIFIER | c.376+1828T>C | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 4/12 | chr19 | 48907713 | |||||||
| chr19:48907743 | C | A | 1 | a0001c0001t0002g0121 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.376+1858C>A | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 4/12 | chr19 | 48907743 | |||||||
| chr19:48907769 | G | A | 3 | a0001c0001t0001g0384 a0001c0001t0001g0385 a0001c0001t0001g0386 |
3 | NA18950.hp2 NA18977.hp1 NA19054.hp2 |
intron_variant | MODIFIER | c.376+1884G>A | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 4/12 | chr19 | 48907769 | |||||||
| chr19:48907775 | A | G | 55 | a0001c0001t0001g0009 a0001c0001t0001g0090 a0001c0001t0001g0113 others(52): Show |
57 | HG00621.hp2 HG01993.hp2 HG02055.hp2 others(54): Show |
intron_variant | MODIFIER | c.376+1890A>G | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 4/12 | chr19 | 48907775 | |||||||
| chr19:48907822 | G | A | 1 | a0001c0001t0002g0290 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.376+1937G>A | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 4/12 | chr19 | 48907822 | |||||||
| chr19:48907841 | G | C | 176 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(173): Show |
180 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(177): Show |
intron_variant | MODIFIER | c.376+1956G>C | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 4/12 | chr19 | 48907841 | |||||||
| chr19:48907914 | C | G | 1 | a0001c0001t0001g0279 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.376+2029C>G | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 4/12 | chr19 | 48907914 | |||||||
| chr19:48907941 | T | G | 26 | a0001c0001t0001g0004 a0001c0001t0001g0088 a0001c0001t0001g0119 others(23): Show |
27 | HG00408.hp2 HG00621.hp1 HG01081.hp1 others(24): Show |
intron_variant | MODIFIER | c.376+2056T>G | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 4/12 | chr19 | 48907941 | |||||||
| chr19:48908033 | G | T | 3 | a0001c0001t0001g0300 a0001c0001t0001g0301 a0001c0001t0001g0302 |
3 | HG01346.hp2 HG02965.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.376+2148G>T | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 4/12 | chr19 | 48908033 | |||||||
| chr19:48908303 | T | C | 15 | a0001c0002t0001g0100 a0001c0002t0002g0091 a0001c0002t0002g0092 others(12): Show |
15 | HG00140.hp2 HG00741.hp2 HG01074.hp1 others(12): Show |
intron_variant | MODIFIER | c.376+2418T>C | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 4/12 | chr19 | 48908303 | |||||||
| chr19:48908311 | G | A | 1 | a0001c0001t0001g0165 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.376+2426G>A | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 4/12 | chr19 | 48908311 | |||||||
| chr19:48908329 | C | T | 1 | a0001c0001t0001g0299 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.376+2444C>T | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 4/12 | chr19 | 48908329 | |||||||
| chr19:48908604 | G | A | 2 | a0001c0001t0001g0167 a0001c0001t0008g0166 |
2 | HG02559.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.377-2545G>A | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 4/12 | chr19 | 48908604 | |||||||
| chr19:48908648 | C | CGT | 38 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0033 others(35): Show |
39 | HG00099.hp1 HG00558.hp1 HG00597.hp1 others(36): Show |
intron_variant | MODIFIER | c.377-2452_377-2451d others(4): Show |
NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr19 | 48908648 | ||||||
| chr19:48908648 | C | CGTGT | 56 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0042 others(53): Show |
57 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(54): Show |
intron_variant | MODIFIER | c.377-2454_377-2451d others(6): Show |
NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr19 | 48908648 | ||||||
| chr19:48908648 | C | CGTGTGT | 52 | a0001c0001t0001g0007 a0001c0001t0001g0024 a0001c0001t0001g0048 others(49): Show |
53 | HG00609.hp2 HG00642.hp2 HG00735.hp2 others(50): Show |
intron_variant | MODIFIER | c.377-2456_377-2451d others(8): Show |
NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr19 | 48908648 | ||||||
| chr19:48908648 | C | CGTGTGTG others(1): Show |
35 | a0001c0001t0001g0054 a0001c0001t0001g0122 a0001c0001t0001g0133 others(32): Show |
35 | HG00423.hp2 HG00642.hp1 HG01346.hp2 others(32): Show |
intron_variant | MODIFIER | c.377-2458_377-2451d others(10): Show |
NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr19 | 48908648 | ||||||
| chr19:48908648 | C | CGTGTGTG others(3): Show |
36 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0015 others(33): Show |
38 | HG00280.hp1 HG00544.hp2 HG00621.hp1 others(35): Show |
intron_variant | MODIFIER | c.377-2460_377-2451d others(12): Show |
NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr19 | 48908648 | ||||||
| chr19:48908648 | C | CGTGTGTG others(5): Show |
27 | a0001c0001t0001g0064 a0001c0001t0001g0112 a0001c0001t0001g0163 others(24): Show |
27 | HG00438.hp1 HG00597.hp2 HG00733.hp1 others(24): Show |
intron_variant | MODIFIER | c.377-2462_377-2451d others(14): Show |
NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr19 | 48908648 | ||||||
| chr19:48908648 | C | CGTGTGTG others(7): Show |
17 | a0001c0001t0001g0066 a0001c0001t0001g0067 a0001c0001t0001g0106 others(14): Show |
18 | HG00408.hp1 HG01255.hp1 HG02129.hp1 others(15): Show |
intron_variant | MODIFIER | c.377-2464_377-2451d others(16): Show |
NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr19 | 48908648 | ||||||
| chr19:48908648 | C | CGTGTGTG others(9): Show |
13 | a0001c0001t0001g0004 a0001c0001t0001g0119 a0001c0001t0001g0138 others(10): Show |
14 | HG00408.hp2 HG00544.hp1 HG01981.hp1 others(11): Show |
intron_variant | MODIFIER | c.377-2466_377-2451d others(18): Show |
NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr19 | 48908648 | ||||||
| chr19:48908648 | C | CGTGTGTG others(11): Show |
4 | a0001c0001t0001g0071 a0001c0001t0001g0277 a0001c0001t0001g0389 others(1): Show |
4 | HG01258.hp1 NA18999.hp1 NA19012.hp1 others(1): Show |
intron_variant | MODIFIER | c.377-2468_377-2451d others(20): Show |
NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr19 | 48908648 | ||||||
| chr19:48908648 | C | CGTGTGTG others(13): Show |
1 | a0001c0001t0002g0278 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.377-2470_377-2451d others(22): Show |
NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr19 | 48908648 | ||||||
| chr19:48908648 | C | CTGTGTGT others(10): Show |
1 | a0001c0001t0001g0139 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.377-2501_377-2500i others(19): Show |
NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 4/12 | chr19 | 48908648 | |||||||
| chr19:48908648 | CGT | C | 25 | a0001c0001t0001g0027 a0001c0001t0001g0083 a0001c0001t0001g0174 others(22): Show |
25 | HG00621.hp2 HG01123.hp2 HG01257.hp1 others(22): Show |
intron_variant | MODIFIER | c.377-2452_377-2451d others(4): Show |
NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr19 | 48908648 | ||||||
| chr19:48908648 | CGTGT | C | 11 | a0001c0001t0001g0305 a0001c0001t0001g0306 a0001c0001t0001g0307 others(8): Show |
11 | HG02055.hp2 HG02155.hp2 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.377-2454_377-2451d others(6): Show |
NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr19 | 48908648 | ||||||
| chr19:48908648 | CGTGTGT | C | 6 | a0001c0001t0001g0169 a0001c0001t0001g0381 a0001c0001t0002g0170 others(3): Show |
6 | HG00438.hp2 HG00609.hp1 HG01993.hp2 others(3): Show |
intron_variant | MODIFIER | c.377-2456_377-2451d others(8): Show |
NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr19 | 48908648 | ||||||
| chr19:48908648 | CGTGTGTG others(3): Show |
C | 2 | a0001c0002t0001g0100 a0001c0002t0002g0101 |
2 | HG01099.hp2 HG01109.hp1 |
intron_variant | MODIFIER | c.377-2460_377-2451d others(12): Show |
NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr19 | 48908648 | ||||||
| chr19:48908648 | CGTGTGTG others(5): Show |
C | 13 | a0001c0001t0001g0168 a0001c0002t0002g0091 a0001c0002t0002g0092 others(10): Show |
13 | HG00140.hp2 HG00741.hp2 HG01074.hp1 others(10): Show |
intron_variant | MODIFIER | c.377-2462_377-2451d others(14): Show |
NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr19 | 48908648 | ||||||
| chr19:48908648 | CGTGTGTG others(7): Show |
C | 2 | a0001c0001t0002g0140 a0002c0004t0001g0026 |
2 | HG02922.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.377-2464_377-2451d others(16): Show |
NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr19 | 48908648 | ||||||
| chr19:48908648 | CGTGTGTG others(23): Show |
C | 1 | a0001c0001t0002g0373 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.377-2480_377-2451d others(32): Show |
NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr19 | 48908648 | ||||||
| chr19:48908718 | A | AGG | 34 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0027 others(31): Show |
35 | HG01109.hp2 HG01243.hp2 HG01891.hp2 others(32): Show |
intron_variant | MODIFIER | c.377-2428_377-2427d others(4): Show |
NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr19 | 48908718 | ||||||
| chr19:48908719 | G | GGGGT | 23 | a0001c0001t0001g0009 a0001c0001t0001g0113 a0001c0001t0001g0306 others(20): Show |
25 | HG00621.hp2 HG02055.hp2 HG02622.hp2 others(22): Show |
intron_variant | MODIFIER | c.377-2428_377-2425d others(6): Show |
NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr19 | 48908719 | ||||||
| chr19:48908721 | G | GGGGT | 18 | a0001c0001t0001g0038 a0001c0001t0001g0181 a0001c0001t0002g0056 others(15): Show |
18 | HG00733.hp2 HG00735.hp1 HG01070.hp1 others(15): Show |
intron_variant | MODIFIER | c.377-2427_377-2426i others(6): Show |
NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr19 | 48908721 | ||||||
| chr19:48908721 | G | GGGGTGTG others(3): Show |
1 | a0001c0002t0002g0104 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.377-2427_377-2426i others(12): Show |
NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr19 | 48908721 | ||||||
| chr19:48908721 | G | GGT | 61 | a0001c0001t0001g0011 a0001c0001t0001g0031 a0001c0001t0001g0050 others(58): Show |
61 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(58): Show |
intron_variant | MODIFIER | c.377-2387_377-2386d others(4): Show |
NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr19 | 48908721 | ||||||
| chr19:48908721 | G | GGTGGGT | 4 | a0001c0001t0001g0377 a0001c0001t0002g0351 a0001c0001t0002g0352 others(1): Show |
4 | HG03710.hp2 NA19083.hp1 NA20752.hp1 others(1): Show |
intron_variant | MODIFIER | c.377-2425_377-2424i others(8): Show |
NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr19 | 48908721 | ||||||
| chr19:48908721 | G | GGTGGGTG others(1): Show |
9 | a0001c0001t0001g0307 a0001c0001t0001g0345 a0001c0001t0001g0381 others(6): Show |
9 | HG01993.hp2 HG02132.hp2 HG02300.hp2 others(6): Show |
intron_variant | MODIFIER | c.377-2425_377-2424i others(10): Show |
NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr19 | 48908721 | ||||||
| chr19:48908721 | G | GGTGGGTG others(3): Show |
4 | a0001c0001t0001g0090 a0001c0001t0001g0346 a0001c0001t0001g0366 others(1): Show |
4 | HG03831.hp2 HG03942.hp1 NA19079.hp2 others(1): Show |
intron_variant | MODIFIER | c.377-2425_377-2424i others(12): Show |
NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr19 | 48908721 | ||||||
| chr19:48908721 | G | GGTGGGTG others(5): Show |
3 | a0001c0001t0001g0340 a0001c0001t0001g0343 a0001c0001t0002g0350 |
3 | NA18747.hp1 NA18955.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.377-2425_377-2424i others(14): Show |
NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr19 | 48908721 | ||||||
| chr19:48908721 | G | GGTGGGTG others(7): Show |
2 | a0001c0001t0001g0341 a0001c0001t0002g0356 |
2 | HG02155.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.377-2425_377-2424i others(16): Show |
NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr19 | 48908721 | ||||||
| chr19:48908721 | G | GGTGGGTG others(9): Show |
1 | a0001c0001t0001g0348 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.377-2425_377-2424i others(18): Show |
NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr19 | 48908721 | ||||||
| chr19:48908721 | G | GGTGGGTG others(11): Show |
1 | a0001c0001t0001g0342 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.377-2425_377-2424i others(20): Show |
NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr19 | 48908721 | ||||||
| chr19:48908721 | G | GGTGGTGT others(4): Show |
1 | a0001c0001t0001g0344 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.377-2425_377-2424i others(13): Show |
NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr19 | 48908721 | ||||||
| chr19:48908721 | G | GGTGT | 18 | a0001c0001t0001g0002 a0001c0001t0001g0032 a0001c0001t0001g0075 others(15): Show |
19 | HG00423.hp1 HG01255.hp1 HG01515.hp2 others(16): Show |
intron_variant | MODIFIER | c.377-2389_377-2386d others(6): Show |
NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr19 | 48908721 | ||||||
| chr19:48908721 | G | GGTGTGT | 9 | a0001c0001t0001g0006 a0001c0001t0001g0221 a0001c0001t0002g0152 others(6): Show |
10 | HG00597.hp2 HG01358.hp2 HG01975.hp1 others(7): Show |
intron_variant | MODIFIER | c.377-2391_377-2386d others(8): Show |
NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr19 | 48908721 | ||||||
| chr19:48908721 | G | GGTGTGTG others(1): Show |
7 | a0001c0002t0001g0100 a0001c0002t0002g0093 a0001c0002t0002g0094 others(4): Show |
7 | HG00140.hp2 HG00741.hp2 HG01099.hp2 others(4): Show |
intron_variant | MODIFIER | c.377-2393_377-2386d others(10): Show |
NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr19 | 48908721 | ||||||
| chr19:48908721 | G | GGTGTGTG others(3): Show |
3 | a0001c0002t0002g0101 a0001c0002t0002g0103 a0001c0002t0007g0098 |
3 | HG01109.hp1 HG01192.hp1 HG01358.hp1 |
intron_variant | MODIFIER | c.377-2395_377-2386d others(12): Show |
NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr19 | 48908721 | ||||||
| chr19:48908721 | G | GGTGTGTG others(5): Show |
1 | a0001c0002t0002g0099 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.377-2397_377-2386d others(14): Show |
NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr19 | 48908721 | ||||||
| chr19:48908721 | G | GT | 4 | a0001c0001t0001g0119 a0001c0001t0001g0239 a0001c0001t0001g0316 others(1): Show |
4 | HG01255.hp2 HG02523.hp1 NA18995.hp1 others(1): Show |
intron_variant | MODIFIER | c.377-2428_377-2427i others(3): Show |
NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 4/12 | chr19 | 48908721 | |||||||
| chr19:48908721 | G | GTGTGT | 3 | a0001c0001t0002g0252 a0001c0001t0005g0260 a0001c0001t0005g0268 |
3 | HG02148.hp1 HG02148.hp2 HG02300.hp1 |
intron_variant | MODIFIER | c.377-2428_377-2427i others(7): Show |
NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 4/12 | chr19 | 48908721 | |||||||
| chr19:48908721 | GGT | G | 12 | a0001c0001t0001g0045 a0001c0001t0001g0169 a0001c0001t0001g0272 others(9): Show |
12 | HG00609.hp1 HG01256.hp2 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.377-2387_377-2386d others(4): Show |
NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr19 | 48908721 | ||||||
| chr19:48908721 | GGTGT | G | 21 | a0001c0001t0001g0120 a0001c0001t0001g0158 a0001c0001t0001g0159 others(18): Show |
21 | HG00140.hp1 HG00733.hp1 HG00735.hp2 others(18): Show |
intron_variant | MODIFIER | c.377-2389_377-2386d others(6): Show |
NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr19 | 48908721 | ||||||
| chr19:48908721 | GGTGTGT | G | 6 | a0001c0001t0001g0083 a0001c0001t0001g0151 a0001c0001t0001g0300 others(3): Show |
6 | HG00438.hp1 HG01106.hp2 HG01346.hp2 others(3): Show |
intron_variant | MODIFIER | c.377-2391_377-2386d others(8): Show |
NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr19 | 48908721 | ||||||
| chr19:48908721 | GGTGTGTG others(5): Show |
G | 3 | a0001c0001t0001g0339 a0001c0001t0016g0338 a0004c0012t0001g0337 |
3 | HG01261.hp1 HG02257.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.377-2397_377-2386d others(14): Show |
NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr19 | 48908721 | ||||||
| chr19:48908723 | T | G | 12 | a0001c0001t0001g0197 a0001c0001t0001g0223 a0001c0001t0001g0312 others(9): Show |
12 | HG00558.hp1 HG01978.hp2 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.377-2426T>G | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 4/12 | chr19 | 48908723 | |||||||
| chr19:48908723 | T | TGG | 4 | a0001c0001t0001g0305 a0001c0001t0001g0308 a0001c0001t0001g0367 others(1): Show |
4 | HG02896.hp2 HG02897.hp1 NA18962.hp2 others(1): Show |
intron_variant | MODIFIER | c.377-2425_377-2424i others(4): Show |
NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr19 | 48908723 | ||||||
| chr19:48908725 | T | G | 2 | a0001c0001t0001g0336 a0001c0011t0002g0334 |
2 | HG02280.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.377-2424T>G | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 4/12 | chr19 | 48908725 | |||||||
| chr19:48908844 | C | A | 15 | a0001c0002t0001g0100 a0001c0002t0002g0091 a0001c0002t0002g0092 others(12): Show |
15 | HG00140.hp2 HG00741.hp2 HG01074.hp1 others(12): Show |
intron_variant | MODIFIER | c.377-2305C>A | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 4/12 | chr19 | 48908844 | |||||||
| chr19:48909142 | T | G | 1 | a0001c0001t0001g0317 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.377-2007T>G | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 4/12 | chr19 | 48909142 | |||||||
| chr19:48909248 | TA | T | 23 | a0001c0001t0001g0064 a0001c0001t0001g0075 a0001c0001t0001g0309 others(20): Show |
23 | HG01070.hp2 HG01071.hp2 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.377-1900delA | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 4/12 | chr19 | 48909248 | |||||||
| chr19:48909249 | A | T | 7 | a0001c0001t0001g0007 a0001c0001t0001g0230 a0001c0001t0001g0274 others(4): Show |
7 | HG01081.hp2 HG01255.hp2 HG02015.hp1 others(4): Show |
intron_variant | MODIFIER | c.377-1900A>T | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 4/12 | chr19 | 48909249 | |||||||
| chr19:48909249 | AT | A | 79 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(76): Show |
81 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(78): Show |
intron_variant | MODIFIER | c.377-1887delT | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr19 | 48909249 | ||||||
| chr19:48909252 | T | A | 23 | a0001c0001t0001g0158 a0001c0001t0001g0190 a0001c0001t0002g0135 others(20): Show |
23 | HG00099.hp1 HG00140.hp2 HG00642.hp1 others(20): Show |
intron_variant | MODIFIER | c.377-1897T>A | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 4/12 | chr19 | 48909252 | |||||||
| chr19:48909253 | T | A | 9 | a0001c0001t0001g0027 a0001c0001t0001g0033 a0001c0001t0001g0038 others(6): Show |
9 | HG00733.hp2 HG00735.hp1 HG01109.hp2 others(6): Show |
intron_variant | MODIFIER | c.377-1896T>A | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 4/12 | chr19 | 48909253 | |||||||
| chr19:48909255 | T | A | 15 | a0001c0002t0001g0100 a0001c0002t0002g0091 a0001c0002t0002g0092 others(12): Show |
15 | HG00140.hp2 HG00741.hp2 HG01074.hp1 others(12): Show |
intron_variant | MODIFIER | c.377-1894T>A | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 4/12 | chr19 | 48909255 | |||||||
| chr19:48909261 | T | C | 4 | a0001c0001t0001g0325 a0001c0001t0001g0327 a0001c0001t0001g0383 others(1): Show |
4 | HG02145.hp1 HG02630.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.377-1888T>C | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 4/12 | chr19 | 48909261 | |||||||
| chr19:48909262 | T | C | 26 | a0001c0001t0001g0106 a0001c0001t0001g0300 a0001c0001t0001g0301 others(23): Show |
26 | HG01070.hp2 HG01071.hp2 HG01255.hp2 others(23): Show |
intron_variant | MODIFIER | c.377-1887T>C | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 4/12 | chr19 | 48909262 | |||||||
| chr19:48909283 | C | T | 11 | a0001c0001t0001g0015 a0001c0001t0002g0017 a0001c0001t0010g0021 others(8): Show |
12 | HG01891.hp2 HG02257.hp2 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.377-1866C>T | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 4/12 | chr19 | 48909283 | |||||||
| chr19:48909396 | C | T | 1 | a0001c0001t0001g0375 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.377-1753C>T | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 4/12 | chr19 | 48909396 | |||||||
| chr19:48909447 | A | G | 2 | a0001c0001t0002g0371 a0001c0001t0002g0376 |
2 | HG02738.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.377-1702A>G | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 4/12 | chr19 | 48909447 | |||||||
| chr19:48909568 | T | G | 1 | a0001c0001t0001g0201 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.377-1581T>G | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 4/12 | chr19 | 48909568 | |||||||
| chr19:48909580 | C | T | 1 | a0001c0001t0001g0300 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.377-1569C>T | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 4/12 | chr19 | 48909580 | |||||||
| chr19:48909752 | C | T | 1 | a0001c0001t0002g0216 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.377-1397C>T | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 4/12 | chr19 | 48909752 | |||||||
| chr19:48909931 | A | T | 2 | a0001c0001t0001g0010 a0001c0001t0001g0037 |
2 | HG02622.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.377-1218A>T | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 4/12 | chr19 | 48909931 | |||||||
| chr19:48909979 | T | C | 23 | a0001c0001t0001g0309 a0001c0001t0001g0310 a0001c0001t0001g0311 others(20): Show |
23 | HG01070.hp2 HG01071.hp2 HG01255.hp2 others(20): Show |
intron_variant | MODIFIER | c.377-1170T>C | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 4/12 | chr19 | 48909979 | |||||||
| chr19:48910002 | T | C | 162 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(159): Show |
166 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(163): Show |
intron_variant | MODIFIER | c.377-1147T>C | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 4/12 | chr19 | 48910002 | |||||||
| chr19:48910073 | G | A | 3 | a0001c0001t0002g0116 a0001c0001t0002g0143 a0001c0001t0002g0262 |
3 | HG00733.hp1 HG01256.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.377-1076G>A | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 4/12 | chr19 | 48910073 | |||||||
| chr19:48910102 | C | T | 1 | a0001c0001t0002g0156 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.377-1047C>T | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 4/12 | chr19 | 48910102 | |||||||
| chr19:48910242 | A | G | 1 | a0001c0003t0001g0335 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.377-907A>G | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 4/12 | chr19 | 48910242 | |||||||
| chr19:48910368 | A | G | 6 | a0002c0004t0001g0026 a0002c0004t0001g0035 a0002c0004t0001g0036 others(3): Show |
6 | HG02486.hp1 HG02717.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.377-781A>G | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 4/12 | chr19 | 48910368 | |||||||
| chr19:48910405 | G | A | 19 | a0001c0001t0001g0298 a0001c0001t0001g0299 a0001c0001t0002g0202 others(16): Show |
19 | HG00140.hp2 HG00280.hp2 HG00741.hp2 others(16): Show |
intron_variant | MODIFIER | c.377-744G>A | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 4/12 | chr19 | 48910405 | |||||||
| chr19:48910562 | T | C | 19 | a0001c0001t0001g0298 a0001c0001t0001g0299 a0001c0001t0002g0202 others(16): Show |
19 | HG00140.hp2 HG00280.hp2 HG00741.hp2 others(16): Show |
intron_variant | MODIFIER | c.377-587T>C | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 4/12 | chr19 | 48910562 | |||||||
| chr19:48910634 | G | A | 9 | a0001c0001t0001g0300 a0001c0001t0001g0301 a0001c0001t0001g0302 others(6): Show |
9 | HG01346.hp2 HG02486.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.377-515G>A | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 4/12 | chr19 | 48910634 | |||||||
| chr19:48910665 | C | G | 5 | a0001c0001t0001g0298 a0001c0001t0001g0299 a0001c0001t0013g0297 others(2): Show |
5 | HG01433.hp1 HG01884.hp1 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.377-484C>G | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 4/12 | chr19 | 48910665 | |||||||
| chr19:48910672 | CA | C | 9 | a0001c0001t0001g0277 a0001c0001t0001g0311 a0001c0001t0001g0342 others(6): Show |
9 | HG01070.hp2 HG01257.hp2 HG01517.hp1 others(6): Show |
intron_variant | MODIFIER | c.377-462delA | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr19 | 48910672 | ||||||
| chr19:48911328 | G | A | 5 | a0001c0001t0001g0298 a0001c0001t0001g0299 a0001c0001t0013g0297 others(2): Show |
5 | HG01433.hp1 HG01884.hp1 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.480+76G>A | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 5/12 | chr19 | 48911328 | |||||||
| chr19:48911385 | T | C | 1 | a0001c0001t0001g0083 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.480+133T>C | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 5/12 | chr19 | 48911385 | |||||||
| chr19:48911391 | GTTTCT | G | 69 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0015 others(66): Show |
71 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(68): Show |
intron_variant | MODIFIER | c.480+153_480+157del others(5): Show |
NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr19 | 48911391 | ||||||
| chr19:48911405 | C | CT | 13 | a0001c0001t0001g0060 a0001c0001t0001g0300 a0001c0001t0001g0301 others(10): Show |
13 | HG01255.hp1 HG01346.hp2 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.480+170dupT | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr19 | 48911405 | ||||||
| chr19:48911405 | CT | C | 57 | a0001c0001t0001g0009 a0001c0001t0001g0090 a0001c0001t0001g0106 others(54): Show |
59 | HG00621.hp2 HG00642.hp1 HG01261.hp2 others(56): Show |
intron_variant | MODIFIER | c.480+170delT | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr19 | 48911405 | ||||||
| chr19:48911475 | G | A | 56 | a0001c0001t0001g0009 a0001c0001t0001g0090 a0001c0001t0001g0336 others(53): Show |
58 | HG00621.hp2 HG00642.hp1 HG01261.hp2 others(55): Show |
intron_variant | MODIFIER | c.480+223G>A | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 5/12 | chr19 | 48911475 | |||||||
| chr19:48911562 | C | T | 10 | a0001c0001t0001g0060 a0001c0001t0001g0300 a0001c0001t0001g0301 others(7): Show |
10 | HG01346.hp2 HG02109.hp1 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.480+310C>T | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 5/12 | chr19 | 48911562 | |||||||
| chr19:48911639 | C | T | 2 | a0001c0001t0001g0299 a0001c0001t0013g0297 |
2 | HG01884.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.480+387C>T | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 5/12 | chr19 | 48911639 | |||||||
| chr19:48911874 | C | T | 19 | a0001c0001t0001g0298 a0001c0001t0001g0299 a0001c0001t0002g0202 others(16): Show |
19 | HG00140.hp2 HG00280.hp2 HG00741.hp2 others(16): Show |
intron_variant | MODIFIER | c.480+622C>T | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 5/12 | chr19 | 48911874 | |||||||
| chr19:48911993 | C | A | 1 | a0001c0001t0001g0190 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.480+741C>A | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 5/12 | chr19 | 48911993 | |||||||
| chr19:48912019 | C | CT | 19 | a0001c0001t0001g0088 a0001c0001t0001g0201 a0001c0001t0001g0383 others(16): Show |
19 | HG00140.hp2 HG00280.hp2 HG00741.hp2 others(16): Show |
intron_variant | MODIFIER | c.480+786dupT | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr19 | 48912019 | ||||||
| chr19:48912019 | CT | C | 151 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(148): Show |
155 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(152): Show |
intron_variant | MODIFIER | c.480+786delT | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr19 | 48912019 | ||||||
| chr19:48912104 | A | T | 1 | a0001c0001t0001g0186 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.480+852A>T | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 5/12 | chr19 | 48912104 | |||||||
| chr19:48912129 | A | G | 1 | a0001c0001t0009g0329 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.480+877A>G | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 5/12 | chr19 | 48912129 | |||||||
| chr19:48912179 | C | T | 16 | a0001c0001t0001g0298 a0001c0001t0001g0299 a0001c0001t0002g0202 others(13): Show |
16 | HG00140.hp2 HG00280.hp2 HG00741.hp2 others(13): Show |
intron_variant | MODIFIER | c.481-832C>T | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 5/12 | chr19 | 48912179 | |||||||
| chr19:48912225 | T | C | 20 | a0001c0001t0001g0113 a0001c0001t0001g0274 a0001c0001t0001g0305 others(17): Show |
20 | HG00140.hp2 HG00280.hp2 HG00741.hp2 others(17): Show |
intron_variant | MODIFIER | c.481-786T>C | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 5/12 | chr19 | 48912225 | |||||||
| chr19:48912311 | C | T | 1 | a0001c0001t0003g0114 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.481-700C>T | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 5/12 | chr19 | 48912311 | |||||||
| chr19:48912377 | G | T | 73 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(70): Show |
75 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(72): Show |
intron_variant | MODIFIER | c.481-634G>T | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 5/12 | chr19 | 48912377 | |||||||
| chr19:48912561 | C | T | 2 | a0001c0001t0002g0214 a0001c0001t0002g0215 |
2 | NA19007.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.481-450C>T | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 5/12 | chr19 | 48912561 | |||||||
| chr19:48912604 | C | G | 103 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(100): Show |
106 | HG00280.hp1 HG00408.hp1 HG00544.hp1 others(103): Show |
intron_variant | MODIFIER | c.481-407C>G | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 5/12 | chr19 | 48912604 | |||||||
| chr19:48912627 | G | A | 1 | a0001c0001t0001g0203 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.481-384G>A | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 5/12 | chr19 | 48912627 | |||||||
| chr19:48912665 | G | A | 2 | a0001c0001t0002g0214 a0001c0001t0002g0215 |
2 | NA19007.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.481-346G>A | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 5/12 | chr19 | 48912665 | |||||||
| chr19:48912704 | C | T | 1 | a0001c0001t0001g0389 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.481-307C>T | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 5/12 | chr19 | 48912704 | |||||||
| chr19:48912711 | C | T | 1 | a0001c0001t0002g0365 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.481-300C>T | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 5/12 | chr19 | 48912711 | |||||||
| chr19:48912714 | T | TA | 27 | a0001c0001t0001g0034 a0001c0001t0001g0060 a0001c0001t0001g0300 others(24): Show |
27 | HG00140.hp2 HG00280.hp2 HG01074.hp1 others(24): Show |
intron_variant | MODIFIER | c.481-295dupA | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr19 | 48912714 | ||||||
| chr19:48912760 | C | T | 1 | a0001c0001t0005g0182 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.481-251C>T | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 5/12 | chr19 | 48912760 | |||||||
| chr19:48912843 | C | CA | 49 | a0001c0001t0001g0009 a0001c0001t0001g0079 a0001c0001t0001g0158 others(46): Show |
51 | HG00140.hp2 HG00438.hp1 HG00609.hp2 others(48): Show |
intron_variant | MODIFIER | c.481-149dupA | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr19 | 48912843 | ||||||
| chr19:48912843 | C | CAA | 14 | a0001c0001t0001g0015 a0001c0001t0001g0083 a0001c0001t0001g0106 others(11): Show |
14 | HG01433.hp1 HG01884.hp1 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.481-150_481-149dup others(2): Show |
NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr19 | 48912843 | ||||||
| chr19:48912843 | C | CAAA | 28 | a0001c0001t0001g0011 a0001c0001t0001g0034 a0001c0001t0001g0037 others(25): Show |
28 | HG00733.hp2 HG01070.hp1 HG01243.hp2 others(25): Show |
intron_variant | MODIFIER | c.481-151_481-149dup others(3): Show |
NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr19 | 48912843 | ||||||
| chr19:48912843 | C | CAAAA | 13 | a0001c0001t0001g0010 a0001c0001t0001g0060 a0001c0001t0001g0300 others(10): Show |
13 | HG01346.hp2 HG02055.hp1 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.481-152_481-149dup others(4): Show |
NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr19 | 48912843 | ||||||
| chr19:48912843 | CA | C | 89 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0031 others(86): Show |
92 | HG00408.hp1 HG00544.hp1 HG00544.hp2 others(89): Show |
intron_variant | MODIFIER | c.481-149delA | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr19 | 48912843 | ||||||
| chr19:48912914 | C | T | 2 | a0001c0002t0002g0091 a0001c0002t0002g0105 |
2 | HG01358.hp2 HG02602.hp2 |
intron_variant | MODIFIER | c.481-97C>T | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 5/12 | chr19 | 48912914 | |||||||
| chr19:48913199 | G | A | 205 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(202): Show |
213 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(210): Show |
splice_region_variant&intron_variant | LOW | c.666+3G>A | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 6/12 | chr19 | 48913199 | |||||||
| chr19:48913208 | A | G | 1 | a0001c0001t0002g0373 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.666+12A>G | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 6/12 | chr19 | 48913208 | |||||||
| chr19:48913246 | C | T | 1 | a0001c0001t0001g0106 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.666+50C>T | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 6/12 | chr19 | 48913246 | |||||||
| chr19:48913247 | G | C | 13 | a0001c0001t0001g0010 a0001c0001t0001g0079 a0001c0001t0001g0300 others(10): Show |
13 | HG01255.hp2 HG01346.hp2 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.666+51G>C | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 6/12 | chr19 | 48913247 | |||||||
| chr19:48913297 | C | CA | 7 | a0001c0001t0001g0027 a0001c0001t0001g0033 a0001c0001t0001g0034 others(4): Show |
7 | HG01891.hp1 HG02109.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.666+108dupA | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr19 | 48913297 | ||||||
| chr19:48913297 | CA | C | 232 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(229): Show |
238 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(235): Show |
intron_variant | MODIFIER | c.666+108delA | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr19 | 48913297 | ||||||
| chr19:48913679 | C | T | 89 | a0001c0001t0001g0037 a0001c0001t0001g0149 a0001c0001t0001g0165 others(86): Show |
89 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(86): Show |
intron_variant | MODIFIER | c.757+115C>T | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 7/12 | chr19 | 48913679 | |||||||
| chr19:48913723 | G | A | 6 | a0001c0001t0001g0037 a0001c0001t0001g0305 a0001c0001t0001g0306 others(3): Show |
6 | HG01070.hp2 HG01071.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.757+159G>A | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 7/12 | chr19 | 48913723 | |||||||
| chr19:48913731 | G | A | 2 | a0001c0001t0002g0062 a0001c0001t0002g0068 |
2 | NA18966.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.757+167G>A | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 7/12 | chr19 | 48913731 | |||||||
| chr19:48913817 | G | A | 35 | a0001c0001t0001g0002 a0001c0001t0001g0027 a0001c0001t0001g0028 others(32): Show |
36 | HG00544.hp1 HG00642.hp2 HG01175.hp1 others(33): Show |
intron_variant | MODIFIER | c.757+253G>A | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 7/12 | chr19 | 48913817 | |||||||
| chr19:48913941 | G | C | 3 | a0001c0001t0004g0146 a0001c0001t0004g0331 a0001c0008t0012g0014 |
3 | HG02809.hp2 HG03209.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.757+377G>C | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 7/12 | chr19 | 48913941 | |||||||
| chr19:48913968 | C | CT | 30 | a0001c0001t0001g0088 a0001c0001t0001g0122 a0001c0001t0001g0131 others(27): Show |
30 | HG00621.hp1 HG00673.hp1 HG00741.hp2 others(27): Show |
intron_variant | MODIFIER | c.757+421dupT | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 48913968 | ||||||
| chr19:48913971 | T | C | 1 | a0001c0001t0004g0326 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.757+407T>C | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 7/12 | chr19 | 48913971 | |||||||
| chr19:48913989 | A | G | 170 | a0001c0001t0001g0011 a0001c0001t0001g0037 a0001c0001t0001g0088 others(167): Show |
170 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(167): Show |
intron_variant | MODIFIER | c.757+425A>G | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 7/12 | chr19 | 48913989 | |||||||
| chr19:48914068 | C | T | 13 | a0001c0001t0001g0054 a0001c0001t0001g0059 a0001c0001t0001g0075 others(10): Show |
13 | HG01261.hp1 HG01433.hp1 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.757+504C>T | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 7/12 | chr19 | 48914068 | |||||||
| chr19:48914173 | A | T | 1 | a0001c0001t0002g0283 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.757+609A>T | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 7/12 | chr19 | 48914173 | |||||||
| chr19:48914230 | A | C | 216 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0027 others(213): Show |
217 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(214): Show |
intron_variant | MODIFIER | c.757+666A>C | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 7/12 | chr19 | 48914230 | |||||||
| chr19:48914267 | G | A | 2 | a0001c0001t0001g0324 a0001c0001t0001g0332 |
2 | HG01884.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.757+703G>A | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 7/12 | chr19 | 48914267 | |||||||
| chr19:48914401 | T | C | 366 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(363): Show |
375 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(372): Show |
intron_variant | MODIFIER | c.757+837T>C | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 7/12 | chr19 | 48914401 | |||||||
| chr19:48914432 | C | G | 6 | a0001c0001t0001g0059 a0001c0001t0001g0075 a0001c0001t0003g0114 others(3): Show |
6 | HG02109.hp2 HG02970.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.757+868C>G | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 7/12 | chr19 | 48914432 | |||||||
| chr19:48914528 | C | A | 4 | a0001c0001t0001g0299 a0001c0001t0001g0339 a0001c0001t0010g0173 others(1): Show |
4 | HG01884.hp1 HG02257.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.757+964C>A | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 7/12 | chr19 | 48914528 | |||||||
| chr19:48914616 | G | A | 7 | a0001c0001t0001g0059 a0001c0001t0001g0075 a0001c0001t0003g0114 others(4): Show |
7 | HG01433.hp1 HG02109.hp2 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.757+1052G>A | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 7/12 | chr19 | 48914616 | |||||||
| chr19:48914684 | T | C | 236 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0027 others(233): Show |
238 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(235): Show |
intron_variant | MODIFIER | c.757+1120T>C | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 7/12 | chr19 | 48914684 | |||||||
| chr19:48914784 | T | TA | 9 | a0001c0001t0001g0059 a0001c0001t0001g0075 a0001c0001t0002g0363 others(6): Show |
9 | HG01109.hp1 HG01433.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.757+1232dupA | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 48914784 | ||||||
| chr19:48914796 | AT | A | 5 | a0001c0001t0002g0073 a0001c0001t0002g0124 a0001c0001t0002g0172 others(2): Show |
5 | HG01123.hp2 HG01981.hp2 HG02735.hp2 others(2): Show |
intron_variant | MODIFIER | c.757+1233delT | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 7/12 | chr19 | 48914796 | |||||||
| chr19:48914797 | T | A | 181 | a0001c0001t0001g0011 a0001c0001t0001g0037 a0001c0001t0001g0038 others(178): Show |
182 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(179): Show |
intron_variant | MODIFIER | c.757+1233T>A | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 7/12 | chr19 | 48914797 | |||||||
| chr19:48914876 | T | G | 2 | a0001c0001t0002g0276 a0001c0001t0002g0278 |
2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.757+1312T>G | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 7/12 | chr19 | 48914876 | |||||||
| chr19:48914886 | G | C | 2 | a0001c0001t0001g0195 a0001c0001t0001g0384 |
2 | NA18747.hp2 NA18950.hp2 |
intron_variant | MODIFIER | c.757+1322G>C | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 7/12 | chr19 | 48914886 | |||||||
| chr19:48914934 | G | T | 2 | a0001c0003t0001g0295 a0001c0003t0001g0318 |
2 | HG02145.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.757+1370G>T | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 7/12 | chr19 | 48914934 | |||||||
| chr19:48914981 | G | T | 14 | a0001c0001t0001g0011 a0001c0001t0001g0300 a0001c0001t0001g0301 others(11): Show |
14 | HG01346.hp2 HG02055.hp2 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.757+1417G>T | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 7/12 | chr19 | 48914981 | |||||||
| chr19:48915007 | G | A | 7 | a0001c0001t0002g0017 a0001c0001t0002g0148 a0001c0001t0002g0155 others(4): Show |
7 | HG00735.hp2 HG01081.hp1 HG01261.hp2 others(4): Show |
intron_variant | MODIFIER | c.757+1443G>A | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 7/12 | chr19 | 48915007 | |||||||
| chr19:48915111 | G | A | 7 | a0001c0001t0001g0059 a0001c0001t0001g0075 a0001c0001t0003g0114 others(4): Show |
7 | HG01433.hp1 HG02109.hp2 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.757+1547G>A | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 7/12 | chr19 | 48915111 | |||||||
| chr19:48915333 | A | AAAAAC | 248 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(245): Show |
250 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(247): Show |
intron_variant | MODIFIER | c.757+1779_757+1783d others(7): Show |
NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 48915333 | ||||||
| chr19:48915340 | A | AAAC | 129 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(126): Show |
136 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(133): Show |
intron_variant | MODIFIER | c.757+1779_757+1781d others(5): Show |
NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 48915340 | ||||||
| chr19:48915403 | T | C | 234 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0027 others(231): Show |
236 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(233): Show |
intron_variant | MODIFIER | c.757+1839T>C | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 7/12 | chr19 | 48915403 | |||||||
| chr19:48915429 | C | T | 3 | a0001c0001t0001g0339 a0001c0001t0010g0173 a0001c0001t0016g0338 |
3 | HG02257.hp1 HG02615.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.757+1865C>T | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 7/12 | chr19 | 48915429 | |||||||
| chr19:48915451 | G | C | 37 | a0001c0001t0001g0002 a0001c0001t0001g0027 a0001c0001t0001g0028 others(34): Show |
38 | HG00140.hp2 HG00544.hp1 HG01243.hp2 others(35): Show |
intron_variant | MODIFIER | c.757+1887G>C | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 7/12 | chr19 | 48915451 | |||||||
| chr19:48915728 | T | C | 6 | a0001c0001t0001g0037 a0001c0001t0001g0305 a0001c0001t0001g0306 others(3): Show |
6 | HG01070.hp2 HG01071.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.757+2164T>C | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 7/12 | chr19 | 48915728 | |||||||
| chr19:48915761 | G | A | 194 | a0001c0001t0001g0011 a0001c0001t0001g0037 a0001c0001t0001g0038 others(191): Show |
195 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(192): Show |
intron_variant | MODIFIER | c.757+2197G>A | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 7/12 | chr19 | 48915761 | |||||||
| chr19:48915804 | C | T | 1 | a0001c0001t0001g0164 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.757+2240C>T | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 7/12 | chr19 | 48915804 | |||||||
| chr19:48915807 | C | T | 1 | a0001c0001t0001g0139 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.757+2243C>T | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 7/12 | chr19 | 48915807 | |||||||
| chr19:48915810 | G | A | 3 | a0001c0001t0001g0339 a0001c0001t0010g0173 a0001c0001t0016g0338 |
3 | HG02257.hp1 HG02615.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.757+2246G>A | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 7/12 | chr19 | 48915810 | |||||||
| chr19:48916010 | A | G | 164 | a0001c0001t0001g0037 a0001c0001t0001g0088 a0001c0001t0001g0111 others(161): Show |
164 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(161): Show |
intron_variant | MODIFIER | c.757+2446A>G | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 7/12 | chr19 | 48916010 | |||||||
| chr19:48916051 | A | G | 1 | a0001c0001t0008g0166 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.757+2487A>G | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 7/12 | chr19 | 48916051 | |||||||
| chr19:48916171 | C | CGT | 40 | a0001c0001t0001g0002 a0001c0001t0001g0027 a0001c0001t0001g0028 others(37): Show |
41 | HG00140.hp2 HG00544.hp1 HG00609.hp1 others(38): Show |
intron_variant | MODIFIER | c.758-2528_758-2527d others(4): Show |
NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 48916171 | ||||||
| chr19:48916171 | C | CGTGT | 13 | a0001c0001t0001g0302 a0001c0001t0001g0307 a0001c0001t0001g0377 others(10): Show |
13 | HG01261.hp1 HG02145.hp2 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.758-2530_758-2527d others(6): Show |
NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 48916171 | ||||||
| chr19:48916171 | C | CGTGTGTG others(3): Show |
1 | a0001c0001t0004g0319 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.758-2536_758-2527d others(12): Show |
NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 48916171 | ||||||
| chr19:48916171 | C | CGTGTGTG others(5): Show |
2 | a0001c0001t0001g0010 a0001c0001t0004g0326 |
2 | HG03453.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.758-2538_758-2527d others(14): Show |
NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 48916171 | ||||||
| chr19:48916171 | C | CGTGTGTG others(7): Show |
3 | a0001c0001t0001g0011 a0001c0001t0001g0300 a0001c0001t0001g0301 |
3 | HG01346.hp2 HG02965.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.758-2540_758-2527d others(16): Show |
NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 48916171 | ||||||
| chr19:48916171 | C | CGTGTGTG others(9): Show |
5 | a0001c0001t0001g0106 a0001c0001t0006g0078 a0001c0001t0006g0080 others(2): Show |
5 | HG02055.hp2 HG02486.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.758-2542_758-2527d others(18): Show |
NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 48916171 | ||||||
| chr19:48916171 | C | CGTGTGTG others(11): Show |
7 | a0002c0004t0001g0026 a0002c0004t0001g0035 a0002c0004t0001g0036 others(4): Show |
7 | HG02486.hp1 HG02717.hp1 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.758-2544_758-2527d others(20): Show |
NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 48916171 | ||||||
| chr19:48916171 | C | CGTGTGTG others(13): Show |
1 | a0001c0001t0013g0297 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.758-2546_758-2527d others(22): Show |
NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 48916171 | ||||||
| chr19:48916171 | C | T | 10 | a0001c0001t0003g0074 a0001c0001t0003g0161 a0001c0001t0003g0204 others(7): Show |
10 | HG00099.hp1 HG00621.hp1 HG00673.hp1 others(7): Show |
intron_variant | MODIFIER | c.758-2555C>T | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 7/12 | chr19 | 48916171 | |||||||
| chr19:48916171 | CGT | C | 12 | a0001c0001t0001g0325 a0001c0001t0001g0327 a0001c0001t0001g0383 others(9): Show |
13 | HG01516.hp2 HG01517.hp2 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.758-2528_758-2527d others(4): Show |
NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 48916171 | ||||||
| chr19:48916356 | G | A | 1 | a0001c0001t0001g0083 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.758-2370G>A | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 7/12 | chr19 | 48916356 | |||||||
| chr19:48916383 | C | T | 1 | a0001c0001t0002g0188 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.758-2343C>T | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 7/12 | chr19 | 48916383 | |||||||
| chr19:48916393 | G | A | 7 | a0001c0001t0001g0059 a0001c0001t0001g0075 a0001c0001t0003g0114 others(4): Show |
7 | HG01433.hp1 HG02109.hp2 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.758-2333G>A | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 7/12 | chr19 | 48916393 | |||||||
| chr19:48916439 | A | G | 1 | a0001c0001t0002g0294 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.758-2287A>G | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 7/12 | chr19 | 48916439 | |||||||
| chr19:48916583 | GC | G | 32 | a0001c0001t0001g0002 a0001c0001t0001g0027 a0001c0001t0001g0028 others(29): Show |
33 | HG00140.hp2 HG00544.hp1 HG01257.hp1 others(30): Show |
intron_variant | MODIFIER | c.758-2140delC | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 48916583 | ||||||
| chr19:48916646 | A | G | 129 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(126): Show |
136 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(133): Show |
intron_variant | MODIFIER | c.758-2080A>G | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 7/12 | chr19 | 48916646 | |||||||
| chr19:48916654 | A | C | 189 | a0001c0001t0001g0011 a0001c0001t0001g0037 a0001c0001t0001g0038 others(186): Show |
190 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.758-2072A>C | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 7/12 | chr19 | 48916654 | |||||||
| chr19:48916658 | C | T | 1 | a0001c0001t0001g0112 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.758-2068C>T | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 7/12 | chr19 | 48916658 | |||||||
| chr19:48916676 | C | T | 142 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(139): Show |
149 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(146): Show |
intron_variant | MODIFIER | c.758-2050C>T | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 7/12 | chr19 | 48916676 | |||||||
| chr19:48916848 | G | A | 2 | a0001c0001t0002g0152 a0001c0001t0002g0153 |
2 | HG02683.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.758-1878G>A | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 7/12 | chr19 | 48916848 | |||||||
| chr19:48916977 | T | G | 224 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0027 others(221): Show |
226 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(223): Show |
intron_variant | MODIFIER | c.758-1749T>G | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 7/12 | chr19 | 48916977 | |||||||
| chr19:48917056 | T | C | 373 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(370): Show |
382 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(379): Show |
intron_variant | MODIFIER | c.758-1670T>C | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 7/12 | chr19 | 48917056 | |||||||
| chr19:48917407 | C | T | 2 | a0001c0001t0001g0195 a0001c0001t0001g0384 |
2 | NA18747.hp2 NA18950.hp2 |
intron_variant | MODIFIER | c.758-1319C>T | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 7/12 | chr19 | 48917407 | |||||||
| chr19:48917498 | A | T | 13 | a0001c0001t0001g0010 a0001c0001t0001g0106 a0001c0001t0001g0302 others(10): Show |
13 | HG01261.hp1 HG02145.hp2 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.758-1228A>T | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 7/12 | chr19 | 48917498 | |||||||
| chr19:48917498 | AT | A | 175 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0088 others(172): Show |
176 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(173): Show |
intron_variant | MODIFIER | c.758-1218delT | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 48917498 | ||||||
| chr19:48917684 | C | T | 7 | a0001c0001t0001g0059 a0001c0001t0001g0075 a0001c0001t0003g0114 others(4): Show |
7 | HG01433.hp1 HG02109.hp2 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.758-1042C>T | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 7/12 | chr19 | 48917684 | |||||||
| chr19:48917696 | A | G | 2 | a0001c0001t0001g0299 a0001c0001t0008g0166 |
2 | HG01884.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.758-1030A>G | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 7/12 | chr19 | 48917696 | |||||||
| chr19:48917748 | G | A | 1 | a0001c0001t0002g0216 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.758-978G>A | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 7/12 | chr19 | 48917748 | |||||||
| chr19:48917786 | G | A | 1 | a0001c0001t0001g0011 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.758-940G>A | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 7/12 | chr19 | 48917786 | |||||||
| chr19:48917797 | A | G | 222 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0027 others(219): Show |
224 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(221): Show |
intron_variant | MODIFIER | c.758-929A>G | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 7/12 | chr19 | 48917797 | |||||||
| chr19:48917798 | A | T | 1 | a0001c0001t0001g0088 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.758-928A>T | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 7/12 | chr19 | 48917798 | |||||||
| chr19:48917806 | C | CT | 23 | a0001c0001t0001g0281 a0001c0001t0001g0299 a0001c0001t0001g0339 others(20): Show |
23 | HG00438.hp2 HG00597.hp2 HG00741.hp2 others(20): Show |
intron_variant | MODIFIER | c.758-904dupT | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 48917806 | ||||||
| chr19:48917806 | C | CTT | 10 | a0001c0001t0001g0010 a0001c0001t0001g0106 a0001c0001t0001g0302 others(7): Show |
10 | HG01261.hp1 HG02145.hp2 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.758-905_758-904dup others(2): Show |
NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 48917806 | ||||||
| chr19:48917825 | A | G | 7 | a0001c0001t0001g0059 a0001c0001t0001g0075 a0001c0001t0003g0114 others(4): Show |
7 | HG01433.hp1 HG02109.hp2 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.758-901A>G | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 7/12 | chr19 | 48917825 | |||||||
| chr19:48917834 | G | T | 7 | a0001c0001t0001g0059 a0001c0001t0001g0075 a0001c0001t0003g0114 others(4): Show |
7 | HG01433.hp1 HG02109.hp2 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.758-892G>T | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 7/12 | chr19 | 48917834 | |||||||
| chr19:48917879 | A | ATGATC | 141 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(138): Show |
148 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(145): Show |
intron_variant | MODIFIER | c.758-845_758-841dup others(5): Show |
NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 48917879 | ||||||
| chr19:48917894 | C | T | 1 | a0001c0001t0009g0041 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.758-832C>T | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 7/12 | chr19 | 48917894 | |||||||
| chr19:48917935 | T | A | 1 | a0005c0009t0001g0347 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.758-791T>A | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 7/12 | chr19 | 48917935 | |||||||
| chr19:48917995 | G | C | 2 | a0001c0001t0001g0324 a0001c0001t0001g0332 |
2 | HG01884.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.758-731G>C | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 7/12 | chr19 | 48917995 | |||||||
| chr19:48918101 | C | T | 1 | a0001c0001t0001g0120 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.758-625C>T | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 7/12 | chr19 | 48918101 | |||||||
| chr19:48918379 | G | A | 1 | a0001c0001t0001g0375 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.758-347G>A | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 7/12 | chr19 | 48918379 | |||||||
| chr19:48918471 | A | T | 175 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0088 others(172): Show |
176 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(173): Show |
intron_variant | MODIFIER | c.758-255A>T | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 7/12 | chr19 | 48918471 | |||||||
| chr19:48918495 | G | C | 1 | a0001c0001t0002g0244 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.758-231G>C | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 7/12 | chr19 | 48918495 | |||||||
| chr19:48918572 | A | G | 234 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0027 others(231): Show |
236 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(233): Show |
intron_variant | MODIFIER | c.758-154A>G | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 7/12 | chr19 | 48918572 | |||||||
| chr19:48918646 | A | G | 129 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(126): Show |
136 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(133): Show |
intron_variant | MODIFIER | c.758-80A>G | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 7/12 | chr19 | 48918646 | |||||||
| chr19:48918709 | T | C | 221 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0027 others(218): Show |
223 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(220): Show |
intron_variant | MODIFIER | c.758-17T>C | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 7/12 | chr19 | 48918709 | |||||||
| chr19:48918814 | G | A | 1 | a0005c0009t0001g0347 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.816+30G>A | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 8/12 | chr19 | 48918814 | |||||||
| chr19:48918815 | A | G | 1 | a0005c0009t0001g0347 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.816+31A>G | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 8/12 | chr19 | 48918815 | |||||||
| chr19:48918914 | CA | C | 47 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0027 others(44): Show |
48 | HG00140.hp2 HG00544.hp1 HG01257.hp1 others(45): Show |
intron_variant | MODIFIER | c.817-111delA | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr19 | 48918914 | ||||||
| chr19:48918961 | G | C | 12 | a0001c0001t0001g0059 a0001c0001t0001g0075 a0001c0001t0001g0299 others(9): Show |
12 | HG01243.hp2 HG01433.hp1 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.817-69G>C | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 8/12 | chr19 | 48918961 | |||||||
| chr19:48919180 | A | T | 32 | a0001c0001t0001g0002 a0001c0001t0001g0027 a0001c0001t0001g0028 others(29): Show |
33 | HG00140.hp2 HG00544.hp1 HG01257.hp1 others(30): Show |
intron_variant | MODIFIER | c.910-14A>T | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 9/12 | chr19 | 48919180 | |||||||
| chr19:48919305 | C | T | 1 | a0001c0001t0002g0351 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1002+19C>T | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 10/12 | chr19 | 48919305 | |||||||
| chr19:48919395 | C | T | 31 | a0001c0001t0001g0002 a0001c0001t0001g0027 a0001c0001t0001g0028 others(28): Show |
32 | HG00140.hp2 HG00544.hp1 HG01257.hp1 others(29): Show |
intron_variant | MODIFIER | c.1002+109C>T | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 10/12 | chr19 | 48919395 | |||||||
| chr19:48919452 | C | CTTAT | 145 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(142): Show |
152 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(149): Show |
intron_variant | MODIFIER | c.1002+204_1002+207d others(6): Show |
NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr19 | 48919452 | ||||||
| chr19:48919452 | C | CTTATTTA others(1): Show |
5 | a0001c0001t0001g0138 a0001c0001t0001g0307 a0001c0001t0001g0358 others(2): Show |
5 | HG02809.hp1 HG02818.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.1002+200_1002+207d others(10): Show |
NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr19 | 48919452 | ||||||
| chr19:48919452 | C | CTTATTTA others(5): Show |
1 | a0001c0001t0002g0140 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.1002+196_1002+207d others(14): Show |
NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr19 | 48919452 | ||||||
| chr19:48919452 | CTTATTTA others(5): Show |
C | 1 | a0001c0001t0002g0057 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1002+196_1002+207d others(14): Show |
NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr19 | 48919452 | ||||||
| chr19:48919514 | A | G | 362 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(359): Show |
371 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(368): Show |
intron_variant | MODIFIER | c.1002+228A>G | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 10/12 | chr19 | 48919514 | |||||||
| chr19:48919607 | A | G | 3 | a0001c0001t0004g0146 a0001c0001t0004g0331 a0001c0008t0012g0014 |
3 | HG02809.hp2 HG03209.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1002+321A>G | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 10/12 | chr19 | 48919607 | |||||||
| chr19:48919608 | G | T | 3 | a0001c0001t0004g0146 a0001c0001t0004g0331 a0001c0008t0012g0014 |
3 | HG02809.hp2 HG03209.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1002+322G>T | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 10/12 | chr19 | 48919608 | |||||||
| chr19:48919761 | A | AT | 17 | a0001c0001t0001g0300 a0001c0001t0004g0319 a0001c0001t0004g0326 others(14): Show |
17 | HG00099.hp1 HG00741.hp2 HG01099.hp1 others(14): Show |
intron_variant | MODIFIER | c.1002+498dupT | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr19 | 48919761 | ||||||
| chr19:48919781 | TTTTC | T | 12 | a0001c0001t0001g0108 a0001c0001t0001g0218 a0001c0001t0001g0221 others(9): Show |
12 | HG01070.hp1 HG01070.hp2 HG01257.hp1 others(9): Show |
intron_variant | MODIFIER | c.1002+497_1002+500d others(6): Show |
NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr19 | 48919781 | ||||||
| chr19:48919782 | TTTC | T | 161 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(158): Show |
169 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(166): Show |
intron_variant | MODIFIER | c.1002+498_1002+500d others(5): Show |
NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr19 | 48919782 | ||||||
| chr19:48919783 | TTC | T | 154 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0024 others(151): Show |
154 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(151): Show |
intron_variant | MODIFIER | c.1002+499_1002+500d others(4): Show |
NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr19 | 48919783 | ||||||
| chr19:48919784 | TC | T | 22 | a0001c0001t0001g0059 a0001c0001t0001g0106 a0001c0001t0001g0302 others(19): Show |
22 | HG00280.hp1 HG00280.hp2 HG00741.hp1 others(19): Show |
intron_variant | MODIFIER | c.1002+499delC | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 10/12 | chr19 | 48919784 | |||||||
| chr19:48919785 | C | T | 5 | a0001c0001t0001g0075 a0001c0001t0001g0113 a0001c0001t0001g0317 others(2): Show |
5 | HG01261.hp1 HG02055.hp1 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.1002+499C>T | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 10/12 | chr19 | 48919785 | |||||||
| chr19:48919810 | G | A | 1 | a0001c0001t0001g0299 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1002+524G>A | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 10/12 | chr19 | 48919810 | |||||||
| chr19:48919814 | G | T | 37 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0054 others(34): Show |
37 | HG00733.hp2 HG00735.hp1 HG01070.hp1 others(34): Show |
intron_variant | MODIFIER | c.1002+528G>T | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 10/12 | chr19 | 48919814 | |||||||
| chr19:48919838 | G | A | 9 | a0001c0001t0001g0038 a0001c0003t0001g0001 a0001c0003t0001g0012 others(6): Show |
10 | HG01891.hp2 HG02257.hp2 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.1002+552G>A | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 10/12 | chr19 | 48919838 | |||||||
| chr19:48919871 | C | T | 3 | a0001c0001t0001g0010 a0001c0001t0001g0106 a0001c0001t0013g0297 |
3 | HG02965.hp1 HG03453.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1002+585C>T | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 10/12 | chr19 | 48919871 | |||||||
| chr19:48919875 | C | T | 36 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0054 others(33): Show |
36 | HG00733.hp2 HG00735.hp1 HG01070.hp1 others(33): Show |
intron_variant | MODIFIER | c.1002+589C>T | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 10/12 | chr19 | 48919875 | |||||||
| chr19:48919900 | C | T | 1 | a0001c0001t0001g0219 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1002+614C>T | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 10/12 | chr19 | 48919900 | |||||||
| chr19:48920058 | C | T | 26 | a0001c0001t0001g0015 a0001c0001t0001g0054 a0001c0001t0001g0113 others(23): Show |
26 | HG00733.hp2 HG00735.hp1 HG01070.hp1 others(23): Show |
intron_variant | MODIFIER | c.1002+772C>T | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 10/12 | chr19 | 48920058 | |||||||
| chr19:48920107 | G | GC | 375 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(372): Show |
384 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(381): Show |
intron_variant | MODIFIER | c.1002+822dupC | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr19 | 48920107 | ||||||
| chr19:48920119 | G | A | 2 | a0001c0001t0001g0345 a0005c0009t0001g0347 |
2 | HG02132.hp2 NA18992.hp2 |
intron_variant | MODIFIER | c.1002+833G>A | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 10/12 | chr19 | 48920119 | |||||||
| chr19:48920168 | C | T | 1 | a0001c0001t0004g0326 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1002+882C>T | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 10/12 | chr19 | 48920168 | |||||||
| chr19:48920270 | A | G | 5 | a0001c0001t0001g0011 a0001c0001t0001g0301 a0001c0003t0001g0295 others(2): Show |
5 | HG02145.hp2 HG02965.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.1003-884A>G | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 10/12 | chr19 | 48920270 | |||||||
| chr19:48920378 | G | C | 3 | a0001c0001t0006g0078 a0001c0001t0006g0080 a0001c0001t0006g0304 |
3 | HG02055.hp2 HG02486.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.1003-776G>C | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 10/12 | chr19 | 48920378 | |||||||
| chr19:48920448 | T | G | 19 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0042 others(16): Show |
19 | HG00733.hp2 HG01261.hp1 HG01346.hp2 others(16): Show |
intron_variant | MODIFIER | c.1003-706T>G | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 10/12 | chr19 | 48920448 | |||||||
| chr19:48920506 | TTTTA | T | 3 | a0001c0001t0001g0010 a0001c0001t0001g0106 a0001c0001t0013g0297 |
3 | HG02965.hp1 HG03453.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1003-632_1003-629d others(6): Show |
NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr19 | 48920506 | ||||||
| chr19:48920526 | G | A | 142 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(139): Show |
150 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(147): Show |
intron_variant | MODIFIER | c.1003-628G>A | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 10/12 | chr19 | 48920526 | |||||||
| chr19:48920529 | T | G | 1 | a0005c0009t0001g0347 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.1003-625T>G | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 10/12 | chr19 | 48920529 | |||||||
| chr19:48920530 | G | T | 1 | a0005c0009t0001g0347 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.1003-624G>T | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 10/12 | chr19 | 48920530 | |||||||
| chr19:48920599 | T | C | 374 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(371): Show |
383 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(380): Show |
intron_variant | MODIFIER | c.1003-555T>C | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 10/12 | chr19 | 48920599 | |||||||
| chr19:48920704 | G | T | 2 | a0001c0001t0001g0028 a0001c0001t0001g0048 |
2 | HG02717.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.1003-450G>T | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 10/12 | chr19 | 48920704 | |||||||
| chr19:48920782 | G | A | 358 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(355): Show |
367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.1003-372G>A | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 10/12 | chr19 | 48920782 | |||||||
| chr19:48920877 | C | T | 358 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(355): Show |
367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.1003-277C>T | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 10/12 | chr19 | 48920877 | |||||||
| chr19:48920960 | G | A | 356 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(353): Show |
365 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(362): Show |
intron_variant | MODIFIER | c.1003-194G>A | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 10/12 | chr19 | 48920960 | |||||||
| chr19:48920978 | G | A | 10 | a0001c0001t0004g0319 a0001c0001t0004g0326 a0001c0001t0016g0338 others(7): Show |
10 | HG02486.hp1 HG02615.hp2 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.1003-176G>A | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 10/12 | chr19 | 48920978 | |||||||
| chr19:48920990 | C | T | 321 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(318): Show |
329 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(326): Show |
intron_variant | MODIFIER | c.1003-164C>T | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 10/12 | chr19 | 48920990 | |||||||
| chr19:48921009 | A | C | 1 | a0001c0001t0003g0063 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.1003-145A>C | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 10/12 | chr19 | 48921009 | |||||||
| chr19:48921054 | C | A | 10 | a0001c0001t0004g0319 a0001c0001t0004g0326 a0001c0001t0016g0338 others(7): Show |
10 | HG02486.hp1 HG02615.hp2 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.1003-100C>A | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 10/12 | chr19 | 48921054 | |||||||
| chr19:48921097 | C | T | 153 | a0001c0001t0002g0017 a0001c0001t0002g0023 a0001c0001t0002g0025 others(150): Show |
153 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(150): Show |
intron_variant | MODIFIER | c.1003-57C>T | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 10/12 | chr19 | 48921097 | |||||||
| chr19:48921124 | C | A | 153 | a0001c0001t0002g0017 a0001c0001t0002g0023 a0001c0001t0002g0025 others(150): Show |
153 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(150): Show |
intron_variant | MODIFIER | c.1003-30C>A | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 10/12 | chr19 | 48921124 | |||||||
| chr19:48921382 | C | T | 11 | a0001c0003t0001g0001 a0001c0003t0001g0012 a0001c0003t0001g0013 others(8): Show |
12 | HG00733.hp2 HG01433.hp1 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.1173+58C>T | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 11/12 | chr19 | 48921382 | |||||||
| chr19:48921455 | C | T | 1 | a0001c0001t0004g0319 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1173+131C>T | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 11/12 | chr19 | 48921455 | |||||||
| chr19:48921668 | C | T | 153 | a0001c0001t0002g0017 a0001c0001t0002g0023 a0001c0001t0002g0025 others(150): Show |
153 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(150): Show |
intron_variant | MODIFIER | c.1174-159C>T | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 11/12 | chr19 | 48921668 | |||||||
| chr19:48922001 | G | A | 3 | a0001c0001t0001g0042 a0001c0001t0001g0302 a0004c0012t0001g0337 |
3 | HG01261.hp1 HG03225.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1279+69G>A | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 12/12 | chr19 | 48922001 | |||||||
| chr19:48922007 | G | C | 3 | a0001c0001t0001g0042 a0001c0001t0001g0302 a0004c0012t0001g0337 |
3 | HG01261.hp1 HG03225.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1279+75G>C | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 12/12 | chr19 | 48922007 | |||||||
| chr19:48922080 | G | A | 1 | a0001c0001t0002g0072 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1279+148G>A | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 12/12 | chr19 | 48922080 | |||||||
| chr19:48922084 | T | C | 179 | a0001c0001t0001g0015 a0001c0001t0001g0038 a0001c0001t0001g0054 others(176): Show |
179 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(176): Show |
intron_variant | MODIFIER | c.1279+152T>C | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 12/12 | chr19 | 48922084 | |||||||
| chr19:48922085 | C | T | 3 | a0001c0001t0004g0319 a0001c0001t0004g0326 a0001c0001t0016g0338 |
3 | HG02615.hp2 HG02630.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1279+153C>T | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 12/12 | chr19 | 48922085 | |||||||
| chr19:48922134 | G | A | 2 | a0001c0001t0009g0041 a0001c0001t0009g0329 |
2 | HG01243.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.1280-184G>A | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 12/12 | chr19 | 48922134 | |||||||
| chr19:48922134 | GGAGGAGG others(23): Show |
G | 3 | a0001c0001t0004g0319 a0001c0001t0004g0326 a0001c0001t0016g0338 |
3 | HG02615.hp2 HG02630.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1280-169_1280-140d others(32): Show |
NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr19 | 48922134 | ||||||
| chr19:48922146 | GGGACCCC others(29): Show |
G | 10 | a0001c0001t0004g0022 a0001c0001t0004g0146 a0001c0001t0004g0330 others(7): Show |
10 | HG02055.hp2 HG02109.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.1280-154_1280-119d others(38): Show |
NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr19 | 48922146 | ||||||
| chr19:48922280 | G | A | 3 | a0001c0001t0004g0319 a0001c0001t0004g0326 a0001c0001t0016g0338 |
3 | HG02615.hp2 HG02630.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1280-38G>A | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 12/12 | chr19 | 48922280 | |||||||
| chr19:48922289 | G | A | 3 | a0001c0001t0004g0319 a0001c0001t0004g0326 a0001c0001t0016g0338 |
3 | HG02615.hp2 HG02630.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1280-29G>A | NUCB1 | ENSG00000104805.17 | transcript | ENST00000405315.9 | protein_coding | 12/12 | chr19 | 48922289 |