Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 4682 |
| ensemblid | ENSG00000103274.11 |
| hgncid | 8041 |
| symbol | NUBP1 |
| name | NUBP iron-sulfur cluster assembly factor 1, cytosolic |
| refseq_nuc | NM_002484.4 |
| refseq_prot | NP_002475.2 |
| ensembl_nuc | ENST00000283027.10 |
| ensembl_prot | ENSP00000283027.5 |
| mane_status | MANE Select |
| chr | chr16 |
| start | 10743842 |
| end | 10769351 |
| strand | + |
| ver | v1.2 |
| region | chr16:10743842-10769351 |
| region5000 | chr16:10738842-10774351 |
| regionname0 | NUBP1_chr16_10743842_10769351 |
| regionname5000 | NUBP1_chr16_10738842_10774351 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 320 | 381 | 87 | 63 | 185 | 18 | 26 | 136 | NUBP1_chr16_10738842_10774351 | NUBP1 | MEEVP others(315): Show |
chr16 | 10738842 | 10774351 |
| a0002 | 0/0 | 320 | 38 | 7 | 7 | 12 | 0 | 12 | 11 | NUBP1_chr16_10738842_10774351 | NUBP1 | MEEVP others(315): Show |
chr16 | 10738842 | 10774351 |
| a0003 | 0/0 | 320 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | NUBP1_chr16_10738842_10774351 | NUBP1 | MEEVP others(315): Show |
chr16 | 10738842 | 10774351 |
| a0004 | 0/0 | 320 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NUBP1_chr16_10738842_10774351 | NUBP1 | MEAVP others(315): Show |
chr16 | 10738842 | 10774351 |
| a0005 | 0/0 | 320 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NUBP1_chr16_10738842_10774351 | NUBP1 | MEEVP others(315): Show |
chr16 | 10738842 | 10774351 |
| a0006 | 0/0 | 320 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NUBP1_chr16_10738842_10774351 | NUBP1 | MEEVP others(315): Show |
chr16 | 10738842 | 10774351 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 960 | 376 | 83 | 62 | 185 | 18 | 26 | NUBP1_chr16_10738842_10774351 | NUBP1 | ATGGA others(955): Show |
chr16 | 10738842 | 10774351 | ||
| a0001c0003 | 0/0 | 960 | 4 | 4 | 0 | 0 | 0 | 0 | NUBP1_chr16_10738842_10774351 | NUBP1 | ATGGA others(955): Show |
chr16 | 10738842 | 10774351 | ||
| a0001c0005 | 0/0 | 960 | 1 | 0 | 1 | 0 | 0 | 0 | NUBP1_chr16_10738842_10774351 | NUBP1 | ATGGA others(955): Show |
chr16 | 10738842 | 10774351 | ||
| a0002c0002 | 0/0 | 960 | 38 | 7 | 7 | 12 | 0 | 12 | NUBP1_chr16_10738842_10774351 | NUBP1 | ATGGA others(955): Show |
chr16 | 10738842 | 10774351 | ||
| a0003c0004 | 0/0 | 960 | 2 | 0 | 2 | 0 | 0 | 0 | NUBP1_chr16_10738842_10774351 | NUBP1 | ATGGA others(955): Show |
chr16 | 10738842 | 10774351 | ||
| a0004c0008 | 0/0 | 960 | 1 | 1 | 0 | 0 | 0 | 0 | NUBP1_chr16_10738842_10774351 | NUBP1 | ATGGA others(955): Show |
chr16 | 10738842 | 10774351 | ||
| a0005c0006 | 0/0 | 960 | 1 | 1 | 0 | 0 | 0 | 0 | NUBP1_chr16_10738842_10774351 | NUBP1 | ATGGA others(955): Show |
chr16 | 10738842 | 10774351 | ||
| a0006c0007 | 0/0 | 960 | 1 | 0 | 0 | 1 | 0 | 0 | NUBP1_chr16_10738842_10774351 | NUBP1 | ATGGA others(955): Show |
chr16 | 10738842 | 10774351 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 1231 | 235 | 30 | 48 | 124 | 16 | 15 | NUBP1_chr16_10738842_10774351 | NUBP1 | CGAAG others(1226): Show |
chr16 | 10738842 | 10774351 |
| a0001c0001t0002 | 0/0 | 1231 | 123 | 36 | 13 | 61 | 2 | 11 | NUBP1_chr16_10738842_10774351 | NUBP1 | CGAAG others(1226): Show |
chr16 | 10738842 | 10774351 |
| a0001c0001t0003 | 0/0 | 1231 | 10 | 9 | 1 | 0 | 0 | 0 | NUBP1_chr16_10738842_10774351 | NUBP1 | CGAAG others(1226): Show |
chr16 | 10738842 | 10774351 |
| a0001c0001t0004 | 0/0 | 1231 | 5 | 5 | 0 | 0 | 0 | 0 | NUBP1_chr16_10738842_10774351 | NUBP1 | CGAAG others(1226): Show |
chr16 | 10738842 | 10774351 |
| a0001c0001t0005 | 0/0 | 1231 | 3 | 3 | 0 | 0 | 0 | 0 | NUBP1_chr16_10738842_10774351 | NUBP1 | CGAAG others(1226): Show |
chr16 | 10738842 | 10774351 |
| a0001c0003t0001 | 0/0 | 1231 | 4 | 4 | 0 | 0 | 0 | 0 | NUBP1_chr16_10738842_10774351 | NUBP1 | CGAAG others(1226): Show |
chr16 | 10738842 | 10774351 |
| a0001c0005t0001 | 0/0 | 1231 | 1 | 0 | 1 | 0 | 0 | 0 | NUBP1_chr16_10738842_10774351 | NUBP1 | CGAAG others(1226): Show |
chr16 | 10738842 | 10774351 |
| a0002c0002t0001 | 0/0 | 1231 | 33 | 7 | 7 | 7 | 0 | 12 | NUBP1_chr16_10738842_10774351 | NUBP1 | CGAAG others(1226): Show |
chr16 | 10738842 | 10774351 |
| a0002c0002t0002 | 0/0 | 1231 | 5 | 0 | 0 | 5 | 0 | 0 | NUBP1_chr16_10738842_10774351 | NUBP1 | CGAAG others(1226): Show |
chr16 | 10738842 | 10774351 |
| a0003c0004t0001 | 0/0 | 1231 | 2 | 0 | 2 | 0 | 0 | 0 | NUBP1_chr16_10738842_10774351 | NUBP1 | CGAAG others(1226): Show |
chr16 | 10738842 | 10774351 |
| a0004c0008t0002 | 0/0 | 1231 | 1 | 1 | 0 | 0 | 0 | 0 | NUBP1_chr16_10738842_10774351 | NUBP1 | CGAAG others(1226): Show |
chr16 | 10738842 | 10774351 |
| a0005c0006t0001 | 0/0 | 1231 | 1 | 1 | 0 | 0 | 0 | 0 | NUBP1_chr16_10738842_10774351 | NUBP1 | CGAAG others(1226): Show |
chr16 | 10738842 | 10774351 |
| a0006c0007t0001 | 0/0 | 1231 | 1 | 0 | 0 | 1 | 0 | 0 | NUBP1_chr16_10738842_10774351 | NUBP1 | CGAAG others(1226): Show |
chr16 | 10738842 | 10774351 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 18 | 0 | 4 | 12 | 1 | 1 | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| a0001c0001t0001g0003 | 0/0 | 11 | 0 | 0 | 11 | 0 | 0 | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| a0001c0001t0001g0004 | 0/0 | 7 | 0 | 1 | 5 | 0 | 1 | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| a0001c0001t0001g0005 | 0/0 | 8 | 0 | 7 | 1 | 0 | 0 | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| a0001c0001t0001g0006 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| a0001c0001t0001g0007 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| a0001c0001t0001g0010 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| a0001c0001t0001g0011 | 0/0 | 5 | 0 | 1 | 3 | 1 | 0 | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| a0001c0001t0001g0012 | 0/0 | 5 | 0 | 1 | 4 | 0 | 0 | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| a0001c0001t0001g0013 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| a0001c0001t0001g0015 | 0/0 | 4 | 0 | 1 | 2 | 0 | 1 | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| a0001c0001t0001g0016 | 0/0 | 4 | 1 | 3 | 0 | 0 | 0 | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| a0001c0001t0001g0021 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| a0001c0001t0001g0022 | 0/0 | 3 | 0 | 1 | 1 | 1 | 0 | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| a0001c0001t0001g0023 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| a0001c0001t0001g0024 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| a0001c0001t0001g0025 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| a0001c0001t0001g0030 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| a0001c0001t0001g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| a0001c0001t0001g0037 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| a0001c0001t0001g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| a0001c0001t0001g0039 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| a0001c0001t0001g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| a0001c0001t0001g0041 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| a0001c0001t0001g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| a0001c0001t0001g0044 | 1/0 | 2 | 0 | 0 | 1 | 0 | 0 | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| a0001c0001t0001g0045 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| a0001c0001t0001g0046 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| a0001c0001t0001g0047 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| a0001c0001t0001g0048 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| a0001c0001t0001g0049 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| a0001c0001t0001g0050 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| a0001c0001t0001g0146 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| a0001c0001t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| a0001c0001t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| a0001c0001t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| a0001c0001t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| a0001c0001t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| a0001c0001t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| a0001c0001t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| a0001c0001t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| a0001c0001t0001g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| a0001c0001t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| a0001c0001t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| a0001c0001t0001g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| a0001c0001t0002g0002 | 0/0 | 12 | 0 | 2 | 9 | 0 | 1 | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| a0001c0001t0002g0008 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| a0001c0001t0002g0009 | 0/0 | 5 | 0 | 0 | 4 | 0 | 1 | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| a0001c0001t0002g0014 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| a0001c0001t0002g0017 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| a0001c0001t0002g0018 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| a0001c0001t0002g0019 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| a0001c0001t0002g0020 | 0/0 | 3 | 0 | 0 | 0 | 1 | 2 | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| a0001c0001t0002g0032 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| a0001c0001t0002g0033 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| a0001c0001t0002g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| a0001c0001t0002g0035 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| a0001c0001t0002g0051 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| a0001c0001t0002g0055 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| a0001c0001t0002g0056 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| a0001c0001t0002g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| a0001c0001t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| a0001c0001t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| a0001c0001t0002g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| a0001c0001t0002g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| a0001c0001t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| a0001c0001t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| a0001c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| a0001c0001t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| a0001c0001t0002g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| a0001c0001t0002g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| a0001c0001t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| a0001c0001t0002g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| a0001c0001t0002g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| a0001c0001t0002g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| a0001c0001t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| a0001c0001t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| a0001c0001t0002g0091 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| a0001c0001t0002g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| a0001c0001t0002g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| a0001c0001t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| a0001c0001t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| a0001c0001t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| a0001c0001t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| a0001c0001t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| a0001c0001t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| a0001c0001t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| a0001c0001t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| a0001c0001t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| a0001c0001t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| a0001c0001t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| a0001c0001t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| a0001c0001t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| a0001c0001t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| a0001c0001t0002g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| a0001c0001t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| a0001c0001t0002g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| a0001c0001t0002g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| a0001c0001t0002g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| a0001c0001t0002g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| a0001c0001t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| a0001c0001t0002g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| a0001c0001t0002g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| a0001c0001t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| a0001c0001t0002g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| a0001c0001t0002g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| a0001c0001t0002g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| a0001c0001t0002g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| a0001c0001t0002g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| a0001c0001t0002g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| a0001c0001t0002g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| a0001c0001t0002g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| a0001c0001t0002g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| a0001c0001t0002g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| a0001c0001t0002g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| a0001c0001t0002g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| a0001c0001t0002g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| a0001c0001t0002g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| a0001c0001t0002g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| a0001c0001t0002g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| a0001c0001t0002g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| a0001c0001t0002g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| a0001c0001t0002g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| a0001c0001t0002g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| a0001c0001t0002g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| a0001c0001t0002g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| a0001c0001t0003g0053 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| a0001c0001t0003g0054 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| a0001c0001t0003g0057 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| a0001c0001t0003g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| a0001c0001t0003g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| a0001c0001t0003g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| a0001c0001t0003g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| a0001c0001t0004g0026 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| a0001c0001t0004g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| a0001c0001t0004g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| a0001c0001t0005g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| a0001c0001t0005g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| a0001c0003t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| a0001c0003t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| a0001c0003t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| a0001c0003t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| a0001c0005t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| a0002c0002t0001g0027 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| a0002c0002t0001g0028 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| a0002c0002t0001g0029 | 0/0 | 3 | 0 | 1 | 0 | 0 | 2 | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| a0002c0002t0001g0052 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| a0002c0002t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| a0002c0002t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| a0002c0002t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| a0002c0002t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| a0002c0002t0001g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| a0002c0002t0001g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| a0002c0002t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| a0002c0002t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| a0002c0002t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| a0002c0002t0001g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| a0002c0002t0001g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| a0002c0002t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| a0002c0002t0001g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| a0002c0002t0001g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| a0002c0002t0001g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| a0002c0002t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| a0002c0002t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| a0002c0002t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| a0002c0002t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| a0002c0002t0001g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| a0002c0002t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| a0002c0002t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| a0002c0002t0002g0058 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| a0002c0002t0002g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| a0002c0002t0002g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| a0002c0002t0002g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| a0003c0004t0001g0042 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| a0004c0008t0002g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| a0005c0006t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| a0006c0007t0001g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0050 | EUR | GBR | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0022 | EUR | GBR | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0126 | EUR | GBR | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0155 | EUR | GBR | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0076 | EUR | FIN | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0075 | EUR | FIN | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| HG00323 | hp1 | a0001 | c0001 | t0002 | g0020 | EUR | FIN | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | FIN | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | CHS | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| HG00423 | hp1 | a0001 | c0001 | t0002 | g0034 | EAS | CHS | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | CHS | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| HG00438 | hp1 | a0001 | c0001 | t0002 | g0117 | EAS | CHS | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | CHS | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | CHS | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | CHS | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | CHS | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| HG00558 | hp2 | a0001 | c0001 | t0002 | g0085 | EAS | CHS | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | CHS | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | CHS | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| HG00609 | hp1 | a0001 | c0001 | t0002 | g0034 | EAS | CHS | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | CHS | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | CHS | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | CHS | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| HG00639 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0203 | AMR | PUR | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| HG00642 | hp1 | a0001 | c0001 | t0002 | g0035 | AMR | PUR | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0128 | AMR | PUR | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| HG00673 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | CHS | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| HG00673 | hp2 | a0001 | c0001 | t0002 | g0109 | EAS | CHS | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| HG00738 | hp1 | a0002 | c0002 | t0001 | g0061 | AMR | PUR | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| HG01070 | hp1 | a0002 | c0002 | t0001 | g0052 | AMR | PUR | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| HG01070 | hp2 | a0002 | c0002 | t0001 | g0029 | AMR | PUR | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0194 | AMR | PUR | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| HG01071 | hp2 | a0002 | c0002 | t0001 | g0052 | AMR | PUR | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0157 | AMR | PUR | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| HG01081 | hp1 | a0001 | c0001 | t0002 | g0067 | AMR | PUR | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0136 | AMR | PUR | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0125 | AMR | PUR | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0072 | AMR | PUR | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| HG01106 | hp1 | a0001 | c0001 | t0003 | g0252 | AMR | PUR | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0200 | AMR | PUR | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0049 | AMR | PUR | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| HG01109 | hp2 | a0002 | c0002 | t0001 | g0063 | AMR | PUR | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| HG01167 | hp1 | a0001 | c0001 | t0002 | g0055 | AMR | PUR | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0184 | AMR | PUR | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0021 | AMR | PUR | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0022 | AMR | PUR | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0021 | AMR | PUR | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| HG01169 | hp2 | a0001 | c0001 | t0002 | g0055 | AMR | PUR | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0191 | AMR | PUR | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0133 | AMR | PUR | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| HG01192 | hp2 | a0001 | c0001 | t0002 | g0019 | AMR | PUR | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| HG01243 | hp1 | a0001 | c0001 | t0002 | g0014 | AMR | PUR | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| HG01243 | hp2 | a0001 | c0001 | t0002 | g0035 | AMR | PUR | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | CLM | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0204 | AMR | CLM | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0041 | AMR | CLM | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| HG01257 | hp1 | a0003 | c0004 | t0001 | g0042 | AMR | CLM | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| HG01257 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | CLM | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| HG01258 | hp1 | a0003 | c0004 | t0001 | g0042 | AMR | CLM | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0041 | AMR | CLM | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| HG01261 | hp2 | a0002 | c0002 | t0001 | g0239 | AMR | CLM | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| HG01346 | hp1 | a0001 | c0001 | t0002 | g0018 | AMR | CLM | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0156 | AMR | CLM | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0021 | AMR | CLM | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| HG01358 | hp2 | a0002 | c0002 | t0001 | g0240 | AMR | CLM | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | CLM | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| HG01433 | hp1 | a0001 | c0001 | t0002 | g0120 | AMR | CLM | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | CLM | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| HG01496 | hp1 | a0001 | c0005 | t0001 | g0215 | AMR | CLM | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| HG01496 | hp2 | a0001 | c0001 | t0002 | g0019 | AMR | CLM | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0037 | EUR | IBS | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0132 | EUR | IBS | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0140 | EUR | IBS | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0192 | EUR | IBS | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0037 | EUR | IBS | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0190 | EUR | IBS | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0209 | AFR | ACB | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| HG01891 | hp2 | a0001 | c0001 | t0002 | g0255 | AFR | ACB | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0024 | AMR | PEL | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0166 | AMR | PEL | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0202 | AMR | PEL | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0048 | AMR | PEL | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0177 | AMR | PEL | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0048 | AMR | PEL | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0162 | AMR | PEL | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0183 | AMR | PEL | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| HG01978 | hp2 | a0001 | c0001 | t0002 | g0033 | AMR | PEL | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | PEL | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | PEL | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | KHV | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | KHV | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | KHV | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | KHV | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| HG02040 | hp1 | a0001 | c0001 | t0002 | g0094 | EAS | KHV | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | KHV | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| HG02055 | hp1 | a0001 | c0001 | t0002 | g0017 | AFR | ACB | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0217 | AFR | ACB | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | KHV | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| HG02056 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| HG02071 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| HG02071 | hp2 | a0002 | c0002 | t0001 | g0253 | EAS | KHV | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| HG02074 | hp1 | a0001 | c0001 | t0002 | g0009 | EAS | KHV | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | KHV | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| HG02080 | hp1 | a0001 | c0001 | t0002 | g0081 | EAS | KHV | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| HG02080 | hp2 | a0001 | c0001 | t0002 | g0069 | EAS | KHV | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | KHV | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | KHV | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | KHV | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| HG02132 | hp1 | a0001 | c0001 | t0002 | g0079 | EAS | KHV | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | KHV | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| HG02135 | hp1 | a0001 | c0001 | t0002 | g0018 | EAS | KHV | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| HG02135 | hp2 | a0001 | c0001 | t0002 | g0099 | EAS | KHV | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| HG02145 | hp1 | a0001 | c0001 | t0002 | g0083 | AFR | ACB | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0259 | AFR | ACB | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0179 | AMR | PEL | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| HG02155 | hp1 | a0001 | c0001 | t0002 | g0110 | EAS | CDX | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | CDX | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| HG02165 | hp1 | a0001 | c0001 | t0002 | g0101 | EAS | CDX | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | CDX | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| HG02257 | hp1 | a0001 | c0001 | t0004 | g0026 | AFR | ACB | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| HG02257 | hp2 | a0001 | c0001 | t0002 | g0088 | AFR | ACB | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0138 | AFR | ACB | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| HG02258 | hp2 | a0001 | c0001 | t0002 | g0017 | AFR | ACB | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| HG02280 | hp1 | a0001 | c0001 | t0002 | g0269 | AFR | ACB | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| HG02280 | hp2 | a0001 | c0001 | t0002 | g0254 | AFR | ACB | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0124 | AFR | ACB | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| HG02451 | hp2 | a0001 | c0001 | t0002 | g0264 | AFR | ACB | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| HG02523 | hp1 | a0001 | c0001 | t0002 | g0008 | EAS | KHV | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | KHV | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| HG02572 | hp1 | a0001 | c0001 | t0002 | g0270 | AFR | GWD | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| HG02572 | hp2 | a0001 | c0001 | t0002 | g0077 | AFR | GWD | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| HG02602 | hp1 | a0002 | c0002 | t0001 | g0242 | SAS | PJL | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| HG02602 | hp2 | a0002 | c0002 | t0001 | g0028 | SAS | PJL | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| HG02615 | hp1 | a0001 | c0001 | t0002 | g0261 | AFR | GWD | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| HG02615 | hp2 | a0001 | c0001 | t0003 | g0054 | AFR | GWD | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| HG02622 | hp1 | a0001 | c0001 | t0003 | g0249 | AFR | GWD | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| HG02622 | hp2 | a0001 | c0001 | t0003 | g0251 | AFR | GWD | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0260 | AFR | GWD | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| HG02630 | hp2 | a0001 | c0001 | t0005 | g0031 | AFR | GWD | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0030 | AFR | GWD | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| HG02647 | hp2 | a0001 | c0001 | t0002 | g0014 | AFR | GWD | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0123 | SAS | PJL | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| HG02683 | hp2 | a0002 | c0002 | t0001 | g0029 | SAS | PJL | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0139 | AFR | GWD | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| HG02717 | hp2 | a0001 | c0001 | t0002 | g0056 | AFR | GWD | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| HG02723 | hp1 | a0002 | c0002 | t0001 | g0248 | AFR | GWD | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0207 | AFR | GWD | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| HG02735 | hp1 | a0001 | c0001 | t0002 | g0009 | SAS | PJL | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| HG02735 | hp2 | a0002 | c0002 | t0001 | g0233 | SAS | PJL | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0151 | SAS | PJL | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0206 | SAS | PJL | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| HG02809 | hp1 | a0002 | c0002 | t0001 | g0243 | AFR | GWD | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| HG02809 | hp2 | a0002 | c0002 | t0001 | g0246 | AFR | GWD | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| HG02818 | hp1 | a0001 | c0001 | t0002 | g0256 | AFR | GWD | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| HG02818 | hp2 | a0001 | c0001 | t0002 | g0056 | AFR | GWD | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0258 | AFR | GWD | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| HG02886 | hp2 | a0001 | c0001 | t0005 | g0031 | AFR | GWD | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| HG02895 | hp1 | a0001 | c0001 | t0002 | g0087 | AFR | GWD | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| HG02895 | hp2 | a0001 | c0001 | t0002 | g0111 | AFR | GWD | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| HG02896 | hp1 | a0001 | c0001 | t0003 | g0057 | AFR | GWD | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| HG02896 | hp2 | a0001 | c0001 | t0002 | g0112 | AFR | GWD | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| HG02897 | hp1 | a0001 | c0001 | t0003 | g0057 | AFR | GWD | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| HG02897 | hp2 | a0001 | c0001 | t0002 | g0086 | AFR | GWD | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| HG02922 | hp1 | a0001 | c0003 | t0001 | g0218 | AFR | ESN | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| HG02922 | hp2 | a0001 | c0001 | t0002 | g0017 | AFR | ESN | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0188 | AFR | ESN | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| HG02965 | hp2 | a0001 | c0001 | t0002 | g0051 | AFR | ESN | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| HG02970 | hp1 | a0001 | c0001 | t0002 | g0257 | AFR | ESN | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0137 | AFR | ESN | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| HG02976 | hp1 | a0004 | c0008 | t0002 | g0271 | AFR | ESN | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| HG02976 | hp2 | a0001 | c0001 | t0002 | g0113 | AFR | ESN | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| HG03041 | hp1 | a0002 | c0002 | t0001 | g0066 | AFR | GWD | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| HG03041 | hp2 | a0005 | c0006 | t0001 | g0141 | AFR | GWD | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| HG03098 | hp1 | a0001 | c0001 | t0002 | g0226 | AFR | MSL | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| HG03098 | hp2 | a0001 | c0001 | t0003 | g0250 | AFR | MSL | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| HG03130 | hp1 | a0002 | c0002 | t0001 | g0244 | AFR | ESN | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| HG03130 | hp2 | a0001 | c0001 | t0002 | g0014 | AFR | ESN | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| HG03139 | hp1 | a0001 | c0001 | t0002 | g0229 | AFR | ESN | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| HG03139 | hp2 | a0001 | c0001 | t0003 | g0053 | AFR | ESN | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| HG03195 | hp1 | a0001 | c0003 | t0001 | g0221 | AFR | ESN | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| HG03195 | hp2 | a0001 | c0001 | t0004 | g0026 | AFR | ESN | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0145 | AFR | MSL | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0263 | AFR | MSL | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0144 | AFR | MSL | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| HG03225 | hp2 | a0001 | c0001 | t0002 | g0225 | AFR | MSL | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| HG03239 | hp1 | a0002 | c0002 | t0001 | g0241 | SAS | PJL | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0049 | SAS | PJL | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| HG03453 | hp1 | a0001 | c0001 | t0002 | g0119 | AFR | MSL | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| HG03453 | hp2 | a0001 | c0001 | t0002 | g0092 | AFR | MSL | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| HG03486 | hp1 | a0001 | c0001 | t0004 | g0026 | AFR | MSL | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| HG03486 | hp2 | a0001 | c0001 | t0002 | g0017 | AFR | MSL | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| HG03490 | hp1 | a0001 | c0001 | t0002 | g0019 | SAS | PJL | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0039 | SAS | PJL | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0045 | SAS | PJL | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| HG03491 | hp2 | a0002 | c0002 | t0001 | g0029 | SAS | PJL | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0039 | SAS | PJL | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0045 | SAS | PJL | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| HG03516 | hp1 | a0001 | c0001 | t0004 | g0224 | AFR | ESN | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| HG03516 | hp2 | a0001 | c0001 | t0002 | g0014 | AFR | ESN | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| HG03540 | hp1 | a0001 | c0001 | t0004 | g0223 | AFR | GWD | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | GWD | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| HG03579 | hp1 | a0002 | c0002 | t0001 | g0245 | AFR | MSL | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0265 | AFR | MSL | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| HG03654 | hp1 | a0001 | c0001 | t0002 | g0033 | SAS | PJL | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| HG03654 | hp2 | a0001 | c0001 | t0002 | g0084 | SAS | PJL | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| HG03669 | hp1 | a0001 | c0001 | t0002 | g0093 | SAS | PJL | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| HG03669 | hp2 | a0001 | c0001 | t0002 | g0020 | SAS | PJL | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| HG03704 | hp1 | a0001 | c0001 | t0002 | g0032 | SAS | PJL | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| HG03704 | hp2 | a0002 | c0002 | t0001 | g0028 | SAS | PJL | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0205 | SAS | PJL | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| HG03710 | hp2 | a0002 | c0002 | t0001 | g0237 | SAS | PJL | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| HG03831 | hp1 | a0001 | c0001 | t0002 | g0020 | SAS | BEB | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0015 | SAS | BEB | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| HG03834 | hp2 | a0002 | c0002 | t0001 | g0238 | SAS | BEB | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| HG03927 | hp1 | a0001 | c0001 | t0002 | g0147 | SAS | BEB | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0025 | SAS | BEB | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| HG04115 | hp1 | a0002 | c0002 | t0001 | g0232 | SAS | STU | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0208 | SAS | STU | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0199 | SAS | BEB | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| HG04184 | hp2 | a0001 | c0001 | t0002 | g0074 | SAS | BEB | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| HG04228 | hp1 | a0002 | c0002 | t0001 | g0028 | SAS | STU | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| HG04228 | hp2 | a0001 | c0001 | t0002 | g0002 | SAS | STU | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0036 | AFR | YRI | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| NA18522 | hp2 | a0002 | c0002 | t0001 | g0062 | AFR | YRI | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| NA18612 | hp1 | a0001 | c0001 | t0002 | g0068 | EAS | CHB | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | CHB | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| NA18747 | hp1 | a0001 | c0001 | t0002 | g0107 | EAS | CHB | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | CHB | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| NA18906 | hp1 | a0001 | c0003 | t0001 | g0219 | AFR | YRI | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | YRI | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| NA18939 | hp2 | a0001 | c0001 | t0002 | g0100 | EAS | JPT | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| NA18945 | hp2 | a0001 | c0001 | t0002 | g0070 | EAS | JPT | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| NA18948 | hp2 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| NA18949 | hp2 | a0001 | c0001 | t0002 | g0115 | EAS | JPT | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| NA18952 | hp1 | a0001 | c0001 | t0002 | g0018 | EAS | JPT | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| NA18954 | hp1 | a0001 | c0001 | t0002 | g0082 | EAS | JPT | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| NA18957 | hp2 | a0001 | c0001 | t0002 | g0097 | EAS | JPT | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| NA18959 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| NA18960 | hp1 | a0001 | c0001 | t0002 | g0080 | EAS | JPT | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| NA18960 | hp2 | a0002 | c0002 | t0002 | g0058 | EAS | JPT | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| NA18963 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| NA18964 | hp2 | a0001 | c0001 | t0002 | g0032 | EAS | JPT | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| NA18965 | hp2 | a0001 | c0001 | t0002 | g0108 | EAS | JPT | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| NA18966 | hp1 | a0001 | c0001 | t0002 | g0121 | EAS | JPT | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| NA18967 | hp1 | a0001 | c0001 | t0002 | g0106 | EAS | JPT | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| NA18970 | hp1 | a0002 | c0002 | t0001 | g0027 | EAS | JPT | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| NA18971 | hp1 | a0001 | c0001 | t0002 | g0096 | EAS | JPT | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| NA18977 | hp1 | a0002 | c0002 | t0001 | g0027 | EAS | JPT | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| NA18980 | hp2 | a0001 | c0001 | t0002 | g0102 | EAS | JPT | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| NA18983 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| NA18984 | hp2 | a0001 | c0001 | t0002 | g0098 | EAS | JPT | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| NA18988 | hp2 | a0002 | c0002 | t0001 | g0027 | EAS | JPT | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| NA18993 | hp1 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| NA18994 | hp1 | a0001 | c0001 | t0002 | g0090 | EAS | JPT | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| NA18995 | hp1 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| NA18998 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| NA18999 | hp1 | a0002 | c0002 | t0002 | g0267 | EAS | JPT | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| NA19002 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| NA19004 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| NA19005 | hp1 | a0001 | c0001 | t0002 | g0071 | EAS | JPT | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| NA19005 | hp2 | a0001 | c0001 | t0002 | g0118 | EAS | JPT | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| NA19010 | hp1 | a0002 | c0002 | t0002 | g0058 | EAS | JPT | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| NA19012 | hp1 | a0002 | c0002 | t0002 | g0266 | EAS | JPT | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0231 | AFR | LWK | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| NA19030 | hp2 | a0001 | c0001 | t0002 | g0230 | AFR | LWK | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0134 | AFR | LWK | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0135 | AFR | LWK | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| NA19055 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| NA19057 | hp1 | a0002 | c0002 | t0001 | g0235 | EAS | JPT | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| NA19058 | hp1 | a0002 | c0002 | t0002 | g0268 | EAS | JPT | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| NA19060 | hp1 | a0001 | c0001 | t0002 | g0105 | EAS | JPT | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| NA19063 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| NA19064 | hp1 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| NA19065 | hp2 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| NA19068 | hp2 | a0002 | c0002 | t0001 | g0234 | EAS | JPT | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| NA19074 | hp2 | a0001 | c0001 | t0002 | g0078 | EAS | JPT | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| NA19075 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| NA19075 | hp2 | a0001 | c0001 | t0002 | g0114 | EAS | JPT | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| NA19077 | hp1 | a0001 | c0001 | t0002 | g0122 | EAS | JPT | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| NA19078 | hp2 | a0001 | c0001 | t0002 | g0116 | EAS | JPT | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| NA19080 | hp1 | a0001 | c0001 | t0002 | g0089 | EAS | JPT | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| NA19082 | hp2 | a0001 | c0001 | t0002 | g0103 | EAS | JPT | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| NA19084 | hp1 | a0001 | c0001 | t0002 | g0095 | EAS | JPT | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| NA19085 | hp1 | a0001 | c0001 | t0002 | g0131 | EAS | JPT | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| NA19088 | hp2 | a0002 | c0002 | t0001 | g0236 | EAS | JPT | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| NA19089 | hp1 | a0001 | c0001 | t0002 | g0073 | EAS | JPT | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| NA19090 | hp2 | a0006 | c0007 | t0001 | g0004 | EAS | JPT | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0036 | AFR | YRI | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0142 | AFR | YRI | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | ASW | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| NA20129 | hp2 | a0001 | c0001 | t0005 | g0059 | AFR | ASW | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0011 | EUR | TSI | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| NA20752 | hp2 | a0001 | c0001 | t0002 | g0091 | EUR | TSI | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0227 | EUR | TSI | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0153 | EUR | TSI | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | GIH | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| NA20905 | hp2 | a0002 | c0002 | t0001 | g0247 | SAS | GIH | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0050 | AMR | CLM | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0143 | AFR | ACB | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| HG02109 | hp2 | a0001 | c0001 | t0002 | g0222 | AFR | ACB | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| HG02486 | hp1 | a0001 | c0001 | t0002 | g0051 | AFR | ACB | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| HG02486 | hp2 | a0001 | c0001 | t0002 | g0228 | AFR | ACB | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0216 | AFR | ACB | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| HG02559 | hp2 | a0001 | c0001 | t0003 | g0053 | AFR | ACB | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| HG03471 | hp1 | a0001 | c0001 | t0003 | g0054 | AFR | MSL | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| HG03471 | hp2 | a0001 | c0003 | t0001 | g0220 | AFR | MSL | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| NA18955 | hp1 | a0001 | c0001 | t0002 | g0210 | EAS | JPT | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| NA20300 | hp1 | a0001 | c0001 | t0002 | g0127 | AFR | USA | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0262 | AFR | USA | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0185 | AFR | LWK | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0130 | AFR | LWK | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0146 | REF | REF | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0044 | REF | REF | NUBP1_chr16_10738842_10774351 | NUBP1 | chr16 | 10738842 | 10774351 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:10743871 | A | C | 1 | a0004 | 1 | HG02976.hp1 | missense_variant | MODERATE | c.8A>C | p.Glu3Ala | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 1/11 | 30/1231 | 8/963 | 3/320 | chr16 | 10743871 | |||
| chr16:10744056 | C | G | 1 | a0002 | 38 | HG00738.hp1 HG01070.hp1 HG01070.hp2 others(35): Show |
missense_variant | MODERATE | c.115C>G | p.Pro39Ala | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 2/11 | 137/1231 | 115/963 | 39/320 | chr16 | 10744056 | |||
| chr16:10755751 | G | C | 1 | a0003 | 2 | HG01257.hp1 HG01258.hp1 |
missense_variant&splice_region_variant | MODERATE | c.358G>C | p.Val120Leu | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 5/11 | 380/1231 | 358/963 | 120/320 | chr16 | 10755751 | |||
| chr16:10756693 | G | A | 1 | a0005 | 1 | HG03041.hp2 | missense_variant | MODERATE | c.364G>A | p.Val122Met | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 6/11 | 386/1231 | 364/963 | 122/320 | chr16 | 10756693 | |||
| chr16:10757951 | C | T | 1 | a0006 | 1 | NA19090.hp2 | missense_variant | MODERATE | c.530C>T | p.Ser177Leu | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 7/11 | 552/1231 | 530/963 | 177/320 | chr16 | 10757951 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:10752618 | T | C | 2 | a0001c0003 a0001c0005 |
5 | HG01496.hp1 HG02922.hp1 HG03195.hp1 others(2): Show |
synonymous_variant | LOW | c.267T>C | p.Leu89Leu | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 4/11 | 289/1231 | 267/963 | 89/320 | chr16 | 10752618 | |||
| chr16:10756779 | C | T | 1 | a0001c0005 | 1 | HG01496.hp1 | splice_region_variant&synonymous_variant | LOW | c.450C>T | p.Asn150Asn | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 6/11 | 472/1231 | 450/963 | 150/320 | chr16 | 10756779 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:10769107 | A | G | 6 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(3): Show |
147 | HG00323.hp1 HG00423.hp1 HG00438.hp1 others(144): Show |
3_prime_UTR_variant | MODIFIER | c.*2A>G | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 11/11 | 2 | chr16 | 10769107 | ||||||
| chr16:10769108 | C | T | 1 | a0001c0001t0004 | 5 | HG02257.hp1 HG03195.hp2 HG03486.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*3C>T | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 11/11 | 3 | chr16 | 10769108 | ||||||
| chr16:10769193 | G | C | 1 | a0001c0001t0005 | 3 | HG02630.hp2 HG02886.hp2 NA20129.hp2 |
3_prime_UTR_variant | MODIFIER | c.*88G>C | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 11/11 | 88 | chr16 | 10769193 | ||||||
| chr16:10769263 | T | C | 1 | a0001c0001t0003 | 10 | HG01106.hp1 HG02559.hp2 HG02615.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*158T>C | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 11/11 | 158 | chr16 | 10769263 | ||||||
| chr16:10769323 | G | A | 1 | a0001c0001t0005 | 3 | HG02630.hp2 HG02886.hp2 NA20129.hp2 |
3_prime_UTR_variant | MODIFIER | c.*218G>A | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 11/11 | 218 | chr16 | 10769323 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:10743944 | G | C | 2 | a0001c0001t0005g0031 a0001c0001t0005g0059 |
3 | HG02630.hp2 HG02886.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.20-17G>C | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 1/10 | chr16 | 10743944 | |||||||
| chr16:10744216 | G | C | 1 | a0001c0001t0001g0060 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.124+151G>C | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 2/10 | chr16 | 10744216 | |||||||
| chr16:10744238 | T | A | 1 | a0002c0002t0001g0061 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.124+173T>A | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 2/10 | chr16 | 10744238 | |||||||
| chr16:10744248 | G | T | 3 | a0001c0001t0002g0269 a0001c0001t0002g0270 a0004c0008t0002g0271 |
3 | HG02280.hp1 HG02572.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.124+183G>T | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 2/10 | chr16 | 10744248 | |||||||
| chr16:10744253 | G | A | 2 | a0002c0002t0001g0062 a0002c0002t0001g0063 |
2 | HG01109.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.124+188G>A | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 2/10 | chr16 | 10744253 | |||||||
| chr16:10744275 | C | T | 52 | a0001c0001t0001g0030 a0001c0001t0001g0258 a0001c0001t0001g0259 others(49): Show |
70 | HG00738.hp1 HG01070.hp1 HG01070.hp2 others(67): Show |
intron_variant | MODIFIER | c.124+210C>T | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 2/10 | chr16 | 10744275 | |||||||
| chr16:10744278 | T | C | 2 | a0001c0001t0001g0064 a0001c0001t0001g0065 |
2 | NA18957.hp1 NA18977.hp2 |
intron_variant | MODIFIER | c.124+213T>C | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 2/10 | chr16 | 10744278 | |||||||
| chr16:10744297 | A | C | 4 | a0002c0002t0002g0058 a0002c0002t0002g0266 a0002c0002t0002g0267 others(1): Show |
5 | NA18960.hp2 NA18999.hp1 NA19010.hp1 others(2): Show |
intron_variant | MODIFIER | c.124+232A>C | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 2/10 | chr16 | 10744297 | |||||||
| chr16:10744626 | C | G | 3 | a0001c0001t0002g0228 a0001c0001t0002g0229 a0001c0001t0002g0230 |
3 | HG02486.hp2 HG03139.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.124+561C>G | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 2/10 | chr16 | 10744626 | |||||||
| chr16:10744626 | C | T | 1 | a0001c0001t0001g0231 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.124+561C>T | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 2/10 | chr16 | 10744626 | |||||||
| chr16:10744652 | G | C | 27 | a0002c0002t0001g0027 a0002c0002t0001g0028 a0002c0002t0001g0029 others(24): Show |
35 | HG00738.hp1 HG01070.hp1 HG01070.hp2 others(32): Show |
intron_variant | MODIFIER | c.124+587G>C | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 2/10 | chr16 | 10744652 | |||||||
| chr16:10744762 | T | C | 69 | a0001c0001t0001g0072 a0001c0001t0001g0075 a0001c0001t0001g0076 others(66): Show |
102 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(99): Show |
intron_variant | MODIFIER | c.124+697T>C | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 2/10 | chr16 | 10744762 | |||||||
| chr16:10744790 | CTG | C | 6 | a0001c0001t0003g0053 a0001c0001t0003g0054 a0001c0001t0003g0249 others(3): Show |
8 | HG01106.hp1 HG02559.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.124+729_124+730del others(2): Show |
NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr16 | 10744790 | ||||||
| chr16:10744874 | C | T | 1 | a0001c0001t0001g0265 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.124+809C>T | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 2/10 | chr16 | 10744874 | |||||||
| chr16:10744888 | C | G | 1 | a0001c0001t0001g0227 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.124+823C>G | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 2/10 | chr16 | 10744888 | |||||||
| chr16:10744965 | C | G | 1 | a0002c0002t0001g0248 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.124+900C>G | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 2/10 | chr16 | 10744965 | |||||||
| chr16:10745038 | A | G | 142 | a0001c0001t0001g0030 a0001c0001t0001g0072 a0001c0001t0001g0075 others(139): Show |
196 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(193): Show |
intron_variant | MODIFIER | c.124+973A>G | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 2/10 | chr16 | 10745038 | |||||||
| chr16:10745151 | G | A | 83 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(80): Show |
146 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(143): Show |
intron_variant | MODIFIER | c.124+1086G>A | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 2/10 | chr16 | 10745151 | |||||||
| chr16:10745336 | G | A | 1 | a0002c0002t0001g0232 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.124+1271G>A | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 2/10 | chr16 | 10745336 | |||||||
| chr16:10745446 | C | A | 1 | a0001c0001t0001g0185 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.124+1381C>A | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 2/10 | chr16 | 10745446 | |||||||
| chr16:10745458 | GA | G | 14 | a0001c0001t0001g0005 a0001c0001t0001g0024 a0001c0001t0001g0041 others(11): Show |
25 | HG00544.hp2 HG01123.hp1 HG01167.hp2 others(22): Show |
intron_variant | MODIFIER | c.124+1404delA | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr16 | 10745458 | ||||||
| chr16:10745602 | C | T | 1 | a0002c0002t0001g0247 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.124+1537C>T | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 2/10 | chr16 | 10745602 | |||||||
| chr16:10745684 | C | T | 142 | a0001c0001t0001g0030 a0001c0001t0001g0072 a0001c0001t0001g0075 others(139): Show |
196 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(193): Show |
intron_variant | MODIFIER | c.125-1459C>T | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 2/10 | chr16 | 10745684 | |||||||
| chr16:10745706 | G | T | 1 | a0001c0001t0001g0213 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.125-1437G>T | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 2/10 | chr16 | 10745706 | |||||||
| chr16:10745762 | T | C | 47 | a0001c0001t0001g0030 a0001c0001t0001g0258 a0001c0001t0001g0259 others(44): Show |
63 | HG00738.hp1 HG01070.hp1 HG01070.hp2 others(60): Show |
intron_variant | MODIFIER | c.125-1381T>C | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 2/10 | chr16 | 10745762 | |||||||
| chr16:10745801 | G | T | 9 | a0001c0001t0002g0051 a0001c0001t0002g0225 a0001c0001t0002g0226 others(6): Show |
12 | HG02257.hp1 HG02280.hp1 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.125-1342G>T | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 2/10 | chr16 | 10745801 | |||||||
| chr16:10745905 | G | C | 1 | a0002c0002t0001g0233 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.125-1238G>C | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 2/10 | chr16 | 10745905 | |||||||
| chr16:10746050 | A | G | 1 | a0001c0001t0001g0050 | 2 | HG00099.hp1 HG01123.hp2 |
intron_variant | MODIFIER | c.125-1093A>G | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 2/10 | chr16 | 10746050 | |||||||
| chr16:10746064 | G | A | 22 | a0002c0002t0001g0027 a0002c0002t0001g0028 a0002c0002t0001g0029 others(19): Show |
29 | HG00738.hp1 HG01070.hp2 HG01261.hp2 others(26): Show |
intron_variant | MODIFIER | c.125-1079G>A | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 2/10 | chr16 | 10746064 | |||||||
| chr16:10746114 | G | A | 1 | a0001c0005t0001g0215 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.125-1029G>A | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 2/10 | chr16 | 10746114 | |||||||
| chr16:10746263 | T | C | 1 | a0001c0001t0001g0176 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.125-880T>C | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 2/10 | chr16 | 10746263 | |||||||
| chr16:10746328 | C | T | 142 | a0001c0001t0001g0030 a0001c0001t0001g0072 a0001c0001t0001g0075 others(139): Show |
196 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(193): Show |
intron_variant | MODIFIER | c.125-815C>T | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 2/10 | chr16 | 10746328 | |||||||
| chr16:10746509 | G | A | 2 | a0001c0001t0001g0216 a0001c0001t0001g0217 |
2 | HG02055.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.125-634G>A | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 2/10 | chr16 | 10746509 | |||||||
| chr16:10746596 | C | T | 1 | a0001c0001t0002g0122 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.125-547C>T | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 2/10 | chr16 | 10746596 | |||||||
| chr16:10746808 | A | G | 7 | a0001c0001t0002g0051 a0001c0001t0002g0222 a0001c0001t0002g0225 others(4): Show |
10 | HG02109.hp2 HG02257.hp1 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.125-335A>G | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 2/10 | chr16 | 10746808 | |||||||
| chr16:10746923 | G | A | 1 | a0001c0001t0002g0067 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.125-220G>A | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 2/10 | chr16 | 10746923 | |||||||
| chr16:10746990 | C | G | 86 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(83): Show |
149 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(146): Show |
intron_variant | MODIFIER | c.125-153C>G | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 2/10 | chr16 | 10746990 | |||||||
| chr16:10747117 | C | T | 2 | a0001c0001t0005g0031 a0001c0001t0005g0059 |
3 | HG02630.hp2 HG02886.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.125-26C>T | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 2/10 | chr16 | 10747117 | |||||||
| chr16:10747418 | G | C | 1 | a0001c0001t0001g0123 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.258+142G>C | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 3/10 | chr16 | 10747418 | |||||||
| chr16:10747528 | G | A | 1 | a0001c0001t0002g0068 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.258+252G>A | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 3/10 | chr16 | 10747528 | |||||||
| chr16:10747597 | T | C | 3 | a0001c0001t0002g0228 a0001c0001t0002g0229 a0001c0001t0002g0230 |
3 | HG02486.hp2 HG03139.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.258+321T>C | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 3/10 | chr16 | 10747597 | |||||||
| chr16:10747676 | C | G | 70 | a0001c0001t0001g0072 a0001c0001t0001g0075 a0001c0001t0001g0076 others(67): Show |
103 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(100): Show |
intron_variant | MODIFIER | c.258+400C>G | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 3/10 | chr16 | 10747676 | |||||||
| chr16:10747749 | G | C | 69 | a0001c0001t0001g0072 a0001c0001t0001g0075 a0001c0001t0001g0076 others(66): Show |
101 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(98): Show |
intron_variant | MODIFIER | c.258+473G>C | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 3/10 | chr16 | 10747749 | |||||||
| chr16:10747810 | G | A | 1 | a0001c0001t0002g0069 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.258+534G>A | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 3/10 | chr16 | 10747810 | |||||||
| chr16:10747815 | C | T | 6 | a0001c0001t0003g0053 a0001c0001t0003g0054 a0001c0001t0003g0249 others(3): Show |
8 | HG01106.hp1 HG02559.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.258+539C>T | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 3/10 | chr16 | 10747815 | |||||||
| chr16:10747827 | C | G | 1 | a0001c0001t0002g0264 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.258+551C>G | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 3/10 | chr16 | 10747827 | |||||||
| chr16:10748111 | C | T | 1 | a0001c0001t0001g0175 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.258+835C>T | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 3/10 | chr16 | 10748111 | |||||||
| chr16:10748156 | G | T | 55 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(52): Show |
109 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(106): Show |
intron_variant | MODIFIER | c.258+880G>T | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 3/10 | chr16 | 10748156 | |||||||
| chr16:10748428 | T | A | 3 | a0001c0001t0002g0228 a0001c0001t0002g0229 a0001c0001t0002g0230 |
3 | HG02486.hp2 HG03139.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.258+1152T>A | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 3/10 | chr16 | 10748428 | |||||||
| chr16:10748454 | T | C | 3 | a0001c0001t0002g0228 a0001c0001t0002g0229 a0001c0001t0002g0230 |
3 | HG02486.hp2 HG03139.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.258+1178T>C | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 3/10 | chr16 | 10748454 | |||||||
| chr16:10748865 | G | A | 1 | a0001c0001t0001g0177 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.258+1589G>A | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 3/10 | chr16 | 10748865 | |||||||
| chr16:10748867 | A | G | 1 | a0001c0001t0001g0023 | 3 | NA19002.hp1 NA19085.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.258+1591A>G | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 3/10 | chr16 | 10748867 | |||||||
| chr16:10749028 | T | G | 1 | a0001c0001t0001g0124 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.258+1752T>G | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 3/10 | chr16 | 10749028 | |||||||
| chr16:10749050 | T | C | 144 | a0001c0001t0001g0030 a0001c0001t0001g0072 a0001c0001t0001g0075 others(141): Show |
198 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(195): Show |
intron_variant | MODIFIER | c.258+1774T>C | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 3/10 | chr16 | 10749050 | |||||||
| chr16:10749120 | G | GAC | 15 | a0001c0001t0001g0259 a0001c0001t0002g0032 a0001c0001t0002g0056 others(12): Show |
18 | HG01109.hp2 HG02071.hp2 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.258+1848_258+1849d others(4): Show |
NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr16 | 10749120 | ||||||
| chr16:10749120 | G | GACAC | 11 | a0001c0001t0001g0258 a0001c0001t0002g0067 a0001c0001t0002g0083 others(8): Show |
14 | HG00558.hp2 HG01081.hp1 HG01106.hp1 others(11): Show |
intron_variant | MODIFIER | c.258+1846_258+1849d others(6): Show |
NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr16 | 10749120 | ||||||
| chr16:10749120 | G | GACACAC | 4 | a0001c0001t0002g0055 a0001c0001t0002g0256 a0001c0001t0003g0251 others(1): Show |
5 | HG01167.hp1 HG01169.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.258+1849_258+1850i others(8): Show |
NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr16 | 10749120 | ||||||
| chr16:10749120 | G | GACACACA others(1): Show |
4 | a0001c0003t0001g0221 a0002c0002t0001g0066 a0002c0002t0001g0237 others(1): Show |
4 | HG02723.hp1 HG03041.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.258+1849_258+1850i others(10): Show |
NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr16 | 10749120 | ||||||
| chr16:10749120 | G | GACACACA others(3): Show |
3 | a0001c0001t0003g0249 a0001c0001t0003g0250 a0001c0003t0001g0220 |
3 | HG02622.hp1 HG03098.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.258+1849_258+1850i others(12): Show |
NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr16 | 10749120 | ||||||
| chr16:10749120 | G | GACACACA others(5): Show |
1 | a0001c0003t0001g0219 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.258+1849_258+1850i others(14): Show |
NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr16 | 10749120 | ||||||
| chr16:10749120 | G | GACACACA others(13): Show |
1 | a0001c0001t0001g0265 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.258+1849_258+1850i others(22): Show |
NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr16 | 10749120 | ||||||
| chr16:10749120 | G | GACACACA others(19): Show |
1 | a0001c0003t0001g0218 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.258+1849_258+1850i others(28): Show |
NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr16 | 10749120 | ||||||
| chr16:10749120 | GACACAT | G | 9 | a0001c0001t0002g0008 a0001c0001t0002g0019 a0001c0001t0002g0077 others(6): Show |
15 | HG01192.hp2 HG01496.hp2 HG02132.hp1 others(12): Show |
intron_variant | MODIFIER | c.258+1850_258+1855d others(8): Show |
NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr16 | 10749120 | ||||||
| chr16:10749120 | GACACATA others(3): Show |
G | 7 | a0001c0001t0002g0081 a0001c0001t0002g0082 a0001c0001t0002g0257 others(4): Show |
9 | HG02080.hp1 HG02970.hp1 NA18954.hp1 others(6): Show |
intron_variant | MODIFIER | c.258+1850_258+1859d others(12): Show |
NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr16 | 10749120 | ||||||
| chr16:10749120 | GACACATA others(9): Show |
G | 1 | a0001c0001t0002g0264 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.258+1850_258+1865d others(18): Show |
NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr16 | 10749120 | ||||||
| chr16:10749120 | GACACATA others(13): Show |
G | 2 | a0001c0001t0002g0228 a0001c0001t0002g0229 |
2 | HG02486.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.258+1850_258+1869d others(22): Show |
NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr16 | 10749120 | ||||||
| chr16:10749120 | GACACATA others(15): Show |
G | 1 | a0001c0001t0002g0230 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.258+1850_258+1871d others(24): Show |
NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr16 | 10749120 | ||||||
| chr16:10749122 | CACAT | C | 11 | a0001c0001t0001g0072 a0001c0001t0001g0075 a0001c0001t0001g0076 others(8): Show |
14 | HG00280.hp1 HG00280.hp2 HG01099.hp2 others(11): Show |
intron_variant | MODIFIER | c.258+1850_258+1853d others(6): Show |
NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr16 | 10749122 | ||||||
| chr16:10749124 | C | CACACACA others(3): Show |
3 | a0002c0002t0001g0052 a0002c0002t0001g0244 a0002c0002t0001g0245 |
4 | HG01070.hp1 HG01071.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.258+1849_258+1850i others(12): Show |
NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr16 | 10749124 | ||||||
| chr16:10749124 | CAT | C | 33 | a0001c0001t0001g0030 a0001c0001t0001g0262 a0001c0001t0001g0263 others(30): Show |
46 | HG00323.hp1 HG00609.hp1 HG00673.hp2 others(43): Show |
intron_variant | MODIFIER | c.258+1850_258+1851d others(4): Show |
NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr16 | 10749124 | ||||||
| chr16:10749126 | T | C | 76 | a0001c0001t0001g0030 a0001c0001t0001g0104 a0001c0001t0001g0258 others(73): Show |
101 | HG00423.hp1 HG00558.hp2 HG00639.hp1 others(98): Show |
intron_variant | MODIFIER | c.258+1850T>C | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 3/10 | chr16 | 10749126 | |||||||
| chr16:10749126 | T | G | 4 | a0001c0001t0002g0222 a0002c0002t0001g0066 a0002c0002t0001g0237 others(1): Show |
4 | HG02109.hp2 HG02723.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.258+1850T>G | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 3/10 | chr16 | 10749126 | |||||||
| chr16:10749126 | T | TAC | 10 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0025 others(7): Show |
11 | HG00597.hp2 HG00609.hp2 HG01106.hp2 others(8): Show |
intron_variant | MODIFIER | c.258+1893_258+1894d others(4): Show |
NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr16 | 10749126 | ||||||
| chr16:10749126 | T | TACAC | 3 | a0001c0001t0001g0011 a0001c0001t0001g0050 a0001c0001t0001g0201 |
3 | HG00099.hp1 HG00408.hp1 HG01433.hp2 |
intron_variant | MODIFIER | c.258+1891_258+1894d others(6): Show |
NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr16 | 10749126 | ||||||
| chr16:10749126 | TAC | T | 11 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0013 others(8): Show |
16 | HG00099.hp2 HG01934.hp1 HG02015.hp1 others(13): Show |
intron_variant | MODIFIER | c.258+1893_258+1894d others(4): Show |
NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr16 | 10749126 | ||||||
| chr16:10749126 | TACAC | T | 18 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0022 others(15): Show |
30 | HG00140.hp2 HG00408.hp2 HG01071.hp1 others(27): Show |
intron_variant | MODIFIER | c.258+1891_258+1894d others(6): Show |
NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr16 | 10749126 | ||||||
| chr16:10749126 | TACACAC | T | 67 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(64): Show |
111 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(108): Show |
intron_variant | MODIFIER | c.258+1889_258+1894d others(8): Show |
NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr16 | 10749126 | ||||||
| chr16:10749126 | TACACACA others(1): Show |
T | 4 | a0001c0001t0001g0123 a0001c0001t0001g0143 a0001c0001t0001g0154 others(1): Show |
4 | HG02109.hp1 HG02683.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.258+1887_258+1894d others(10): Show |
NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr16 | 10749126 | ||||||
| chr16:10749126 | TACACACA others(3): Show |
T | 2 | a0001c0001t0001g0142 a0001c0001t0001g0144 |
2 | HG03225.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.258+1885_258+1894d others(12): Show |
NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr16 | 10749126 | ||||||
| chr16:10749126 | TACACACA others(5): Show |
T | 2 | a0001c0001t0001g0153 a0001c0001t0001g0209 |
2 | HG01891.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.258+1883_258+1894d others(14): Show |
NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr16 | 10749126 | ||||||
| chr16:10749126 | TACACACA others(21): Show |
T | 1 | a0001c0001t0001g0016 | 3 | HG01255.hp2 HG01361.hp1 HG01993.hp2 |
intron_variant | MODIFIER | c.258+1867_258+1894d others(30): Show |
NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr16 | 10749126 | ||||||
| chr16:10749128 | C | CACACAG | 3 | a0002c0002t0001g0239 a0002c0002t0002g0266 a0002c0002t0002g0267 |
3 | HG01261.hp2 NA18999.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.258+1857_258+1858i others(8): Show |
NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr16 | 10749128 | ||||||
| chr16:10749130 | C | CACAG | 10 | a0002c0002t0001g0028 a0002c0002t0001g0029 a0002c0002t0001g0061 others(7): Show |
15 | HG00738.hp1 HG01070.hp2 HG01358.hp2 others(12): Show |
intron_variant | MODIFIER | c.258+1857_258+1858i others(6): Show |
NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr16 | 10749130 | ||||||
| chr16:10749130 | C | G | 1 | a0001c0001t0002g0226 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.258+1854C>G | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 3/10 | chr16 | 10749130 | |||||||
| chr16:10749134 | C | G | 4 | a0001c0001t0002g0269 a0001c0001t0002g0270 a0002c0002t0001g0233 others(1): Show |
4 | HG02280.hp1 HG02572.hp1 HG02735.hp2 others(1): Show |
intron_variant | MODIFIER | c.258+1858C>G | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 3/10 | chr16 | 10749134 | |||||||
| chr16:10749137 | A | G | 1 | a0001c0001t0001g0212 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.258+1861A>G | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 3/10 | chr16 | 10749137 | |||||||
| chr16:10749140 | C | G | 1 | a0001c0001t0002g0257 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.258+1864C>G | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 3/10 | chr16 | 10749140 | |||||||
| chr16:10749228 | C | T | 144 | a0001c0001t0001g0030 a0001c0001t0001g0072 a0001c0001t0001g0075 others(141): Show |
198 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(195): Show |
intron_variant | MODIFIER | c.258+1952C>T | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 3/10 | chr16 | 10749228 | |||||||
| chr16:10749311 | G | A | 2 | a0001c0001t0001g0186 a0001c0001t0001g0187 |
2 | HG02083.hp1 NA18982.hp2 |
intron_variant | MODIFIER | c.258+2035G>A | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 3/10 | chr16 | 10749311 | |||||||
| chr16:10749436 | A | G | 2 | a0001c0001t0002g0119 a0001c0001t0002g0120 |
2 | HG01433.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.258+2160A>G | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 3/10 | chr16 | 10749436 | |||||||
| chr16:10749456 | G | A | 44 | a0001c0001t0001g0030 a0001c0001t0001g0258 a0001c0001t0001g0259 others(41): Show |
60 | HG00738.hp1 HG01070.hp1 HG01070.hp2 others(57): Show |
intron_variant | MODIFIER | c.258+2180G>A | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 3/10 | chr16 | 10749456 | |||||||
| chr16:10749463 | GA | G | 1 | a0001c0001t0001g0023 | 3 | NA19002.hp1 NA19085.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.258+2189delA | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr16 | 10749463 | ||||||
| chr16:10749517 | T | A | 44 | a0001c0001t0001g0030 a0001c0001t0001g0258 a0001c0001t0001g0259 others(41): Show |
60 | HG00738.hp1 HG01070.hp1 HG01070.hp2 others(57): Show |
intron_variant | MODIFIER | c.258+2241T>A | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 3/10 | chr16 | 10749517 | |||||||
| chr16:10749637 | G | C | 5 | a0001c0003t0001g0218 a0001c0003t0001g0219 a0001c0003t0001g0220 others(2): Show |
5 | HG01496.hp1 HG02922.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.258+2361G>C | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 3/10 | chr16 | 10749637 | |||||||
| chr16:10749798 | G | A | 1 | a0002c0002t0001g0237 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.258+2522G>A | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 3/10 | chr16 | 10749798 | |||||||
| chr16:10749842 | C | T | 1 | a0001c0001t0002g0118 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.258+2566C>T | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 3/10 | chr16 | 10749842 | |||||||
| chr16:10749888 | G | T | 1 | a0001c0001t0001g0213 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.258+2612G>T | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 3/10 | chr16 | 10749888 | |||||||
| chr16:10750056 | G | A | 7 | a0001c0001t0002g0014 a0001c0001t0002g0077 a0001c0001t0002g0083 others(4): Show |
10 | HG01243.hp1 HG02145.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.259-2554G>A | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 3/10 | chr16 | 10750056 | |||||||
| chr16:10750072 | C | T | 1 | a0001c0001t0001g0209 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.259-2538C>T | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 3/10 | chr16 | 10750072 | |||||||
| chr16:10750348 | A | T | 1 | a0001c0001t0002g0117 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.259-2262A>T | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 3/10 | chr16 | 10750348 | |||||||
| chr16:10750421 | T | C | 1 | a0001c0001t0001g0036 | 2 | NA18522.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.259-2189T>C | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 3/10 | chr16 | 10750421 | |||||||
| chr16:10750459 | C | T | 1 | a0001c0001t0001g0263 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.259-2151C>T | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 3/10 | chr16 | 10750459 | |||||||
| chr16:10750484 | C | T | 15 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0040 others(12): Show |
27 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(24): Show |
intron_variant | MODIFIER | c.259-2126C>T | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 3/10 | chr16 | 10750484 | |||||||
| chr16:10750549 | A | T | 4 | a0001c0001t0002g0222 a0001c0001t0002g0228 a0001c0001t0002g0229 others(1): Show |
4 | HG02109.hp2 HG02486.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.259-2061A>T | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 3/10 | chr16 | 10750549 | |||||||
| chr16:10750791 | C | T | 2 | a0001c0001t0002g0270 a0004c0008t0002g0271 |
2 | HG02572.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.259-1819C>T | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 3/10 | chr16 | 10750791 | |||||||
| chr16:10750844 | G | A | 2 | a0001c0001t0002g0086 a0001c0001t0002g0087 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.259-1766G>A | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 3/10 | chr16 | 10750844 | |||||||
| chr16:10750882 | G | A | 2 | a0001c0001t0001g0259 a0001c0001t0001g0260 |
2 | HG02145.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.259-1728G>A | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 3/10 | chr16 | 10750882 | |||||||
| chr16:10751066 | G | A | 6 | a0001c0001t0003g0053 a0001c0001t0003g0054 a0001c0001t0003g0249 others(3): Show |
8 | HG01106.hp1 HG02559.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.259-1544G>A | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 3/10 | chr16 | 10751066 | |||||||
| chr16:10751166 | C | T | 2 | a0001c0001t0001g0216 a0001c0001t0001g0217 |
2 | HG02055.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.259-1444C>T | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 3/10 | chr16 | 10751166 | |||||||
| chr16:10751262 | G | A | 1 | a0002c0002t0001g0248 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.259-1348G>A | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 3/10 | chr16 | 10751262 | |||||||
| chr16:10751314 | T | C | 1 | a0001c0001t0001g0188 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.259-1296T>C | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 3/10 | chr16 | 10751314 | |||||||
| chr16:10751424 | T | C | 3 | a0001c0001t0002g0019 a0001c0001t0002g0033 a0001c0001t0002g0093 |
6 | HG01192.hp2 HG01496.hp2 HG01978.hp2 others(3): Show |
intron_variant | MODIFIER | c.259-1186T>C | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 3/10 | chr16 | 10751424 | |||||||
| chr16:10751531 | A | G | 23 | a0002c0002t0001g0027 a0002c0002t0001g0028 a0002c0002t0001g0029 others(20): Show |
31 | HG00738.hp1 HG01070.hp1 HG01070.hp2 others(28): Show |
intron_variant | MODIFIER | c.259-1079A>G | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 3/10 | chr16 | 10751531 | |||||||
| chr16:10751571 | C | T | 3 | a0001c0001t0001g0030 a0001c0001t0001g0262 a0001c0001t0003g0057 |
6 | HG02647.hp1 HG02896.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.259-1039C>T | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 3/10 | chr16 | 10751571 | |||||||
| chr16:10751605 | G | A | 1 | a0001c0001t0001g0123 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.259-1005G>A | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 3/10 | chr16 | 10751605 | |||||||
| chr16:10751642 | G | A | 1 | a0001c0001t0001g0209 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.259-968G>A | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 3/10 | chr16 | 10751642 | |||||||
| chr16:10751707 | G | A | 1 | a0001c0001t0001g0060 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.259-903G>A | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 3/10 | chr16 | 10751707 | |||||||
| chr16:10751746 | T | C | 1 | a0001c0001t0001g0209 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.259-864T>C | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 3/10 | chr16 | 10751746 | |||||||
| chr16:10751777 | A | G | 1 | a0002c0002t0001g0242 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.259-833A>G | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 3/10 | chr16 | 10751777 | |||||||
| chr16:10751920 | C | T | 16 | a0001c0001t0001g0030 a0001c0001t0001g0258 a0001c0001t0001g0259 others(13): Show |
24 | HG01167.hp1 HG01169.hp2 HG01891.hp2 others(21): Show |
intron_variant | MODIFIER | c.259-690C>T | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 3/10 | chr16 | 10751920 | |||||||
| chr16:10751973 | G | C | 1 | a0001c0001t0002g0055 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.259-637G>C | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 3/10 | chr16 | 10751973 | |||||||
| chr16:10752020 | A | G | 70 | a0001c0001t0001g0072 a0001c0001t0001g0075 a0001c0001t0001g0076 others(67): Show |
102 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(99): Show |
intron_variant | MODIFIER | c.259-590A>G | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 3/10 | chr16 | 10752020 | |||||||
| chr16:10752034 | T | C | 142 | a0001c0001t0001g0030 a0001c0001t0001g0072 a0001c0001t0001g0075 others(139): Show |
195 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(192): Show |
intron_variant | MODIFIER | c.259-576T>C | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 3/10 | chr16 | 10752034 | |||||||
| chr16:10752134 | C | A | 79 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(76): Show |
142 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(139): Show |
intron_variant | MODIFIER | c.259-476C>A | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 3/10 | chr16 | 10752134 | |||||||
| chr16:10752295 | C | T | 1 | a0001c0001t0001g0208 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.259-315C>T | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 3/10 | chr16 | 10752295 | |||||||
| chr16:10752339 | G | A | 1 | a0001c0001t0002g0257 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.259-271G>A | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 3/10 | chr16 | 10752339 | |||||||
| chr16:10752534 | G | A | 1 | a0001c0001t0001g0265 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.259-76G>A | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 3/10 | chr16 | 10752534 | |||||||
| chr16:10752591 | G | T | 1 | a0001c0001t0001g0174 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.259-19G>T | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 3/10 | chr16 | 10752591 | |||||||
| chr16:10752688 | G | A | 1 | a0001c0001t0001g0125 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.327+10G>A | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 4/10 | chr16 | 10752688 | |||||||
| chr16:10752766 | C | T | 2 | a0001c0001t0001g0161 a0001c0001t0001g0162 |
2 | HG01975.hp2 NA18999.hp2 |
intron_variant | MODIFIER | c.327+88C>T | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 4/10 | chr16 | 10752766 | |||||||
| chr16:10752798 | T | C | 1 | a0002c0002t0002g0266 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.327+120T>C | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 4/10 | chr16 | 10752798 | |||||||
| chr16:10752838 | C | T | 1 | a0001c0001t0001g0160 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.327+160C>T | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 4/10 | chr16 | 10752838 | |||||||
| chr16:10752886 | C | T | 1 | a0001c0001t0001g0188 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.327+208C>T | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 4/10 | chr16 | 10752886 | |||||||
| chr16:10752969 | A | G | 1 | a0001c0001t0001g0185 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.327+291A>G | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 4/10 | chr16 | 10752969 | |||||||
| chr16:10753112 | C | G | 77 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(74): Show |
139 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(136): Show |
intron_variant | MODIFIER | c.327+434C>G | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 4/10 | chr16 | 10753112 | |||||||
| chr16:10753123 | C | CAG | 138 | a0001c0001t0001g0030 a0001c0001t0001g0036 a0001c0001t0001g0072 others(135): Show |
186 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(183): Show |
intron_variant | MODIFIER | c.327+446_327+447ins others(2): Show |
NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr16 | 10753123 | ||||||
| chr16:10753271 | G | A | 1 | a0001c0001t0002g0264 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.327+593G>A | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 4/10 | chr16 | 10753271 | |||||||
| chr16:10753311 | G | C | 1 | a0001c0001t0002g0068 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.327+633G>C | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 4/10 | chr16 | 10753311 | |||||||
| chr16:10753497 | TC | T | 3 | a0001c0001t0001g0021 a0001c0001t0001g0037 a0001c0001t0001g0126 |
6 | HG00140.hp1 HG01168.hp1 HG01169.hp1 others(3): Show |
intron_variant | MODIFIER | c.327+824delC | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr16 | 10753497 | ||||||
| chr16:10753527 | C | T | 7 | a0001c0001t0001g0030 a0001c0001t0001g0262 a0001c0001t0002g0017 others(4): Show |
14 | HG01167.hp1 HG01169.hp2 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.327+849C>T | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 4/10 | chr16 | 10753527 | |||||||
| chr16:10753533 | G | C | 5 | a0001c0003t0001g0218 a0001c0003t0001g0219 a0001c0003t0001g0220 others(2): Show |
5 | HG01496.hp1 HG02922.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.327+855G>C | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 4/10 | chr16 | 10753533 | |||||||
| chr16:10753736 | G | A | 2 | a0001c0001t0001g0216 a0001c0001t0001g0217 |
2 | HG02055.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.327+1058G>A | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 4/10 | chr16 | 10753736 | |||||||
| chr16:10753839 | G | A | 5 | a0001c0001t0002g0222 a0001c0001t0002g0228 a0001c0001t0002g0229 others(2): Show |
5 | HG02109.hp2 HG02486.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.327+1161G>A | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 4/10 | chr16 | 10753839 | |||||||
| chr16:10754008 | A | G | 1 | a0001c0001t0001g0159 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.327+1330A>G | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 4/10 | chr16 | 10754008 | |||||||
| chr16:10754046 | T | C | 10 | a0001c0001t0003g0053 a0001c0001t0003g0054 a0001c0001t0003g0057 others(7): Show |
15 | HG01106.hp1 HG02257.hp1 HG02559.hp2 others(12): Show |
intron_variant | MODIFIER | c.327+1368T>C | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 4/10 | chr16 | 10754046 | |||||||
| chr16:10754151 | C | G | 79 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(76): Show |
141 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(138): Show |
intron_variant | MODIFIER | c.327+1473C>G | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 4/10 | chr16 | 10754151 | |||||||
| chr16:10754214 | G | GTTTAT | 96 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(93): Show |
169 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(166): Show |
intron_variant | MODIFIER | c.328-1474_328-1470d others(7): Show |
NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr16 | 10754214 | ||||||
| chr16:10754214 | G | GTTTATTT others(3): Show |
17 | a0001c0001t0001g0036 a0001c0001t0001g0040 a0001c0001t0001g0124 others(14): Show |
20 | HG01433.hp1 HG01496.hp1 HG02109.hp1 others(17): Show |
intron_variant | MODIFIER | c.328-1479_328-1470d others(12): Show |
NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr16 | 10754214 | ||||||
| chr16:10754248 | A | ATTTTATT others(9): Show |
2 | a0001c0001t0001g0216 a0001c0001t0001g0217 |
2 | HG02055.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.328-1470_328-1469i others(18): Show |
NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr16 | 10754248 | ||||||
| chr16:10754306 | G | A | 1 | a0001c0001t0002g0264 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.328-1415G>A | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 4/10 | chr16 | 10754306 | |||||||
| chr16:10754328 | C | T | 4 | a0001c0001t0002g0090 a0001c0001t0002g0114 a0001c0001t0002g0115 others(1): Show |
4 | NA18949.hp2 NA18994.hp1 NA19075.hp2 others(1): Show |
intron_variant | MODIFIER | c.328-1393C>T | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 4/10 | chr16 | 10754328 | |||||||
| chr16:10754336 | G | A | 1 | a0001c0001t0001g0189 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.328-1385G>A | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 4/10 | chr16 | 10754336 | |||||||
| chr16:10754391 | C | T | 1 | a0001c0001t0002g0264 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.328-1330C>T | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 4/10 | chr16 | 10754391 | |||||||
| chr16:10754496 | G | A | 1 | a0001c0001t0001g0209 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.328-1225G>A | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 4/10 | chr16 | 10754496 | |||||||
| chr16:10754503 | G | A | 2 | a0001c0001t0002g0069 a0001c0001t0002g0070 |
2 | HG02080.hp2 NA18945.hp2 |
intron_variant | MODIFIER | c.328-1218G>A | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 4/10 | chr16 | 10754503 | |||||||
| chr16:10754564 | C | T | 8 | a0001c0001t0001g0021 a0001c0001t0001g0037 a0001c0001t0001g0126 others(5): Show |
11 | HG00140.hp1 HG01168.hp1 HG01169.hp1 others(8): Show |
intron_variant | MODIFIER | c.328-1157C>T | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 4/10 | chr16 | 10754564 | |||||||
| chr16:10754584 | C | T | 1 | a0001c0001t0001g0173 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.328-1137C>T | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 4/10 | chr16 | 10754584 | |||||||
| chr16:10754746 | T | C | 5 | a0001c0003t0001g0218 a0001c0003t0001g0219 a0001c0003t0001g0220 others(2): Show |
5 | HG01496.hp1 HG02922.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.328-975T>C | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 4/10 | chr16 | 10754746 | |||||||
| chr16:10754874 | G | A | 2 | a0001c0001t0001g0030 a0001c0001t0001g0262 |
4 | HG02647.hp1 HG03540.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.328-847G>A | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 4/10 | chr16 | 10754874 | |||||||
| chr16:10754986 | A | G | 50 | a0001c0001t0001g0030 a0001c0001t0001g0036 a0001c0001t0001g0258 others(47): Show |
67 | HG00738.hp1 HG01070.hp1 HG01070.hp2 others(64): Show |
intron_variant | MODIFIER | c.328-735A>G | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 4/10 | chr16 | 10754986 | |||||||
| chr16:10755002 | G | A | 2 | a0001c0001t0001g0128 a0001c0001t0002g0127 |
2 | HG00642.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.328-719G>A | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 4/10 | chr16 | 10755002 | |||||||
| chr16:10755060 | A | C | 1 | a0001c0001t0001g0206 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.328-661A>C | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 4/10 | chr16 | 10755060 | |||||||
| chr16:10755095 | T | C | 77 | a0001c0001t0001g0072 a0001c0001t0001g0075 a0001c0001t0001g0076 others(74): Show |
110 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(107): Show |
intron_variant | MODIFIER | c.328-626T>C | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 4/10 | chr16 | 10755095 | |||||||
| chr16:10755135 | C | G | 7 | a0001c0001t0003g0053 a0001c0001t0003g0054 a0001c0001t0003g0057 others(4): Show |
10 | HG01106.hp1 HG02559.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.328-586C>G | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 4/10 | chr16 | 10755135 | |||||||
| chr16:10755463 | A | G | 12 | a0001c0001t0001g0005 a0001c0001t0001g0041 a0001c0001t0001g0148 others(9): Show |
21 | HG00544.hp2 HG01123.hp1 HG01167.hp2 others(18): Show |
intron_variant | MODIFIER | c.328-258A>G | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 4/10 | chr16 | 10755463 | |||||||
| chr16:10755633 | G | A | 3 | a0001c0001t0002g0071 a0001c0001t0002g0078 a0001c0001t0002g0094 |
3 | HG02040.hp1 NA19005.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.328-88G>A | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 4/10 | chr16 | 10755633 | |||||||
| chr16:10755869 | G | A | 20 | a0002c0002t0001g0027 a0002c0002t0001g0028 a0002c0002t0001g0029 others(17): Show |
27 | HG00738.hp1 HG01070.hp2 HG01261.hp2 others(24): Show |
intron_variant | MODIFIER | c.360+116G>A | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 5/10 | chr16 | 10755869 | |||||||
| chr16:10756010 | TAA | T | 1 | a0001c0001t0001g0013 | 5 | HG00609.hp2 NA18971.hp2 NA18982.hp1 others(2): Show |
intron_variant | MODIFIER | c.360+260_360+261del others(2): Show |
NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr16 | 10756010 | ||||||
| chr16:10756283 | G | A | 1 | a0001c0001t0002g0035 | 2 | HG00642.hp1 HG01243.hp2 |
intron_variant | MODIFIER | c.361-407G>A | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 5/10 | chr16 | 10756283 | |||||||
| chr16:10756305 | G | C | 2 | a0001c0001t0001g0216 a0001c0001t0001g0217 |
2 | HG02055.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.361-385G>C | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 5/10 | chr16 | 10756305 | |||||||
| chr16:10756314 | G | A | 1 | a0001c0001t0001g0209 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.361-376G>A | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 5/10 | chr16 | 10756314 | |||||||
| chr16:10756396 | AAAAT | A | 58 | a0001c0001t0001g0016 a0001c0001t0001g0025 a0001c0001t0001g0030 others(55): Show |
78 | HG00099.hp1 HG00738.hp1 HG01070.hp1 others(75): Show |
intron_variant | MODIFIER | c.361-290_361-287del others(4): Show |
NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr16 | 10756396 | ||||||
| chr16:10756454 | C | T | 3 | a0001c0001t0002g0269 a0001c0001t0002g0270 a0004c0008t0002g0271 |
3 | HG02280.hp1 HG02572.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.361-236C>T | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 5/10 | chr16 | 10756454 | |||||||
| chr16:10756559 | C | T | 1 | a0001c0001t0002g0226 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.361-131C>T | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 5/10 | chr16 | 10756559 | |||||||
| chr16:10756560 | A | T | 1 | a0001c0001t0001g0172 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.361-130A>T | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 5/10 | chr16 | 10756560 | |||||||
| chr16:10756659 | G | A | 2 | a0001c0001t0001g0138 a0001c0001t0001g0139 |
2 | HG02258.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.361-31G>A | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 5/10 | chr16 | 10756659 | |||||||
| chr16:10756789 | C | T | 1 | a0001c0001t0003g0250 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.451+9C>T | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 6/10 | chr16 | 10756789 | |||||||
| chr16:10756919 | C | T | 82 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(79): Show |
145 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(142): Show |
intron_variant | MODIFIER | c.451+139C>T | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 6/10 | chr16 | 10756919 | |||||||
| chr16:10756925 | T | C | 5 | a0001c0003t0001g0218 a0001c0003t0001g0219 a0001c0003t0001g0220 others(2): Show |
5 | HG01496.hp1 HG02922.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.451+145T>C | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 6/10 | chr16 | 10756925 | |||||||
| chr16:10757041 | T | G | 1 | a0001c0001t0002g0095 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.451+261T>G | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 6/10 | chr16 | 10757041 | |||||||
| chr16:10757059 | G | C | 1 | a0001c0001t0001g0265 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.451+279G>C | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 6/10 | chr16 | 10757059 | |||||||
| chr16:10757209 | G | A | 3 | a0001c0001t0001g0003 a0001c0001t0001g0043 a0001c0001t0001g0196 |
14 | NA18940.hp2 NA18944.hp1 NA18945.hp1 others(11): Show |
intron_variant | MODIFIER | c.451+429G>A | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 6/10 | chr16 | 10757209 | |||||||
| chr16:10757223 | C | T | 1 | a0003c0004t0001g0042 | 2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.451+443C>T | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 6/10 | chr16 | 10757223 | |||||||
| chr16:10757302 | C | G | 1 | a0005c0006t0001g0141 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.451+522C>G | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 6/10 | chr16 | 10757302 | |||||||
| chr16:10757427 | G | A | 2 | a0001c0001t0001g0216 a0001c0001t0001g0217 |
2 | HG02055.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.452-446G>A | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 6/10 | chr16 | 10757427 | |||||||
| chr16:10757503 | A | G | 75 | a0001c0001t0001g0075 a0001c0001t0001g0076 a0001c0001t0001g0104 others(72): Show |
108 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(105): Show |
intron_variant | MODIFIER | c.452-370A>G | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 6/10 | chr16 | 10757503 | |||||||
| chr16:10757698 | C | A | 2 | a0001c0001t0001g0259 a0001c0001t0001g0260 |
2 | HG02145.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.452-175C>A | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 6/10 | chr16 | 10757698 | |||||||
| chr16:10757766 | C | T | 2 | a0001c0001t0001g0216 a0001c0001t0001g0217 |
2 | HG02055.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.452-107C>T | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 6/10 | chr16 | 10757766 | |||||||
| chr16:10758176 | G | T | 156 | a0001c0001t0001g0016 a0001c0001t0001g0025 a0001c0001t0001g0030 others(153): Show |
215 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(212): Show |
intron_variant | MODIFIER | c.606+149G>T | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 7/10 | chr16 | 10758176 | |||||||
| chr16:10758240 | A | G | 1 | a0001c0001t0002g0077 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.606+213A>G | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 7/10 | chr16 | 10758240 | |||||||
| chr16:10758268 | C | T | 1 | a0001c0001t0001g0123 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.606+241C>T | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 7/10 | chr16 | 10758268 | |||||||
| chr16:10758317 | T | G | 39 | a0001c0001t0001g0072 a0001c0001t0001g0075 a0001c0001t0001g0076 others(36): Show |
67 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(64): Show |
intron_variant | MODIFIER | c.606+290T>G | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 7/10 | chr16 | 10758317 | |||||||
| chr16:10758456 | G | C | 7 | a0001c0001t0003g0053 a0001c0001t0003g0054 a0001c0001t0003g0057 others(4): Show |
10 | HG01106.hp1 HG02559.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.606+429G>C | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 7/10 | chr16 | 10758456 | |||||||
| chr16:10758490 | A | G | 5 | a0001c0003t0001g0218 a0001c0003t0001g0219 a0001c0003t0001g0220 others(2): Show |
5 | HG01496.hp1 HG02922.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.606+463A>G | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 7/10 | chr16 | 10758490 | |||||||
| chr16:10758544 | T | G | 7 | a0001c0001t0003g0053 a0001c0001t0003g0054 a0001c0001t0003g0057 others(4): Show |
10 | HG01106.hp1 HG02559.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.606+517T>G | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 7/10 | chr16 | 10758544 | |||||||
| chr16:10758658 | C | G | 5 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0047 others(2): Show |
15 | HG00609.hp2 HG01943.hp2 HG01975.hp1 others(12): Show |
intron_variant | MODIFIER | c.606+631C>G | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 7/10 | chr16 | 10758658 | |||||||
| chr16:10758709 | T | C | 1 | a0001c0001t0002g0096 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.606+682T>C | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 7/10 | chr16 | 10758709 | |||||||
| chr16:10758801 | G | A | 1 | a0001c0001t0001g0149 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.606+774G>A | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 7/10 | chr16 | 10758801 | |||||||
| chr16:10758862 | G | A | 7 | a0001c0001t0003g0053 a0001c0001t0003g0054 a0001c0001t0003g0057 others(4): Show |
10 | HG01106.hp1 HG02559.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.606+835G>A | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 7/10 | chr16 | 10758862 | |||||||
| chr16:10758927 | T | C | 1 | a0001c0001t0001g0185 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.606+900T>C | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 7/10 | chr16 | 10758927 | |||||||
| chr16:10758944 | G | T | 1 | a0002c0002t0001g0232 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.606+917G>T | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 7/10 | chr16 | 10758944 | |||||||
| chr16:10759197 | T | C | 74 | a0001c0001t0001g0075 a0001c0001t0001g0104 a0001c0001t0002g0002 others(71): Show |
107 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(104): Show |
intron_variant | MODIFIER | c.606+1170T>C | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 7/10 | chr16 | 10759197 | |||||||
| chr16:10759322 | T | C | 15 | a0001c0001t0002g0051 a0001c0001t0002g0222 a0001c0001t0002g0225 others(12): Show |
18 | HG01496.hp1 HG02109.hp2 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.606+1295T>C | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 7/10 | chr16 | 10759322 | |||||||
| chr16:10759478 | T | A | 1 | a0001c0001t0002g0264 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.606+1451T>A | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 7/10 | chr16 | 10759478 | |||||||
| chr16:10759607 | C | T | 7 | a0001c0001t0003g0053 a0001c0001t0003g0054 a0001c0001t0003g0057 others(4): Show |
10 | HG01106.hp1 HG02559.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.606+1580C>T | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 7/10 | chr16 | 10759607 | |||||||
| chr16:10759636 | C | A | 1 | a0001c0001t0001g0216 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.606+1609C>A | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 7/10 | chr16 | 10759636 | |||||||
| chr16:10759642 | G | A | 6 | a0001c0001t0002g0051 a0001c0001t0002g0225 a0001c0001t0002g0226 others(3): Show |
9 | HG02257.hp1 HG02486.hp1 HG02965.hp2 others(6): Show |
intron_variant | MODIFIER | c.606+1615G>A | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 7/10 | chr16 | 10759642 | |||||||
| chr16:10759751 | G | C | 3 | a0001c0001t0002g0269 a0001c0001t0002g0270 a0004c0008t0002g0271 |
3 | HG02280.hp1 HG02572.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.607-1613G>C | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 7/10 | chr16 | 10759751 | |||||||
| chr16:10759862 | T | C | 2 | a0001c0001t0001g0216 a0001c0001t0001g0217 |
2 | HG02055.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.607-1502T>C | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 7/10 | chr16 | 10759862 | |||||||
| chr16:10759909 | G | A | 7 | a0001c0001t0003g0053 a0001c0001t0003g0054 a0001c0001t0003g0057 others(4): Show |
10 | HG01106.hp1 HG02559.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.607-1455G>A | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 7/10 | chr16 | 10759909 | |||||||
| chr16:10759983 | A | G | 6 | a0001c0001t0002g0051 a0001c0001t0002g0225 a0001c0001t0002g0226 others(3): Show |
9 | HG02257.hp1 HG02486.hp1 HG02965.hp2 others(6): Show |
intron_variant | MODIFIER | c.607-1381A>G | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 7/10 | chr16 | 10759983 | |||||||
| chr16:10760006 | T | A | 2 | a0001c0001t0001g0216 a0001c0001t0001g0217 |
2 | HG02055.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.607-1358T>A | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 7/10 | chr16 | 10760006 | |||||||
| chr16:10760011 | G | A | 3 | a0001c0001t0001g0258 a0002c0002t0001g0244 a0002c0002t0001g0246 |
3 | HG02809.hp2 HG02886.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.607-1353G>A | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 7/10 | chr16 | 10760011 | |||||||
| chr16:10760194 | G | T | 3 | a0001c0001t0002g0071 a0001c0001t0002g0078 a0001c0001t0002g0094 |
3 | HG02040.hp1 NA19005.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.607-1170G>T | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 7/10 | chr16 | 10760194 | |||||||
| chr16:10760205 | G | C | 1 | a0001c0001t0002g0081 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.607-1159G>C | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 7/10 | chr16 | 10760205 | |||||||
| chr16:10760233 | G | A | 1 | a0001c0001t0001g0209 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.607-1131G>A | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 7/10 | chr16 | 10760233 | |||||||
| chr16:10760301 | C | T | 15 | a0001c0001t0001g0030 a0001c0001t0001g0262 a0001c0001t0002g0017 others(12): Show |
24 | HG01891.hp2 HG02055.hp1 HG02257.hp1 others(21): Show |
intron_variant | MODIFIER | c.607-1063C>T | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 7/10 | chr16 | 10760301 | |||||||
| chr16:10760319 | G | A | 1 | a0001c0001t0001g0041 | 2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.607-1045G>A | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 7/10 | chr16 | 10760319 | |||||||
| chr16:10760458 | A | T | 3 | a0001c0001t0002g0269 a0001c0001t0002g0270 a0004c0008t0002g0271 |
3 | HG02280.hp1 HG02572.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.607-906A>T | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 7/10 | chr16 | 10760458 | |||||||
| chr16:10760598 | A | G | 221 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(218): Show |
333 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(330): Show |
intron_variant | MODIFIER | c.607-766A>G | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 7/10 | chr16 | 10760598 | |||||||
| chr16:10760696 | C | T | 1 | a0001c0001t0001g0171 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.607-668C>T | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 7/10 | chr16 | 10760696 | |||||||
| chr16:10760735 | TA | T | 9 | a0001c0001t0002g0051 a0001c0001t0002g0225 a0001c0001t0002g0226 others(6): Show |
12 | HG02257.hp1 HG02280.hp1 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.607-619delA | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr16 | 10760735 | ||||||
| chr16:10760803 | C | A | 1 | a0001c0001t0001g0263 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.607-561C>A | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 7/10 | chr16 | 10760803 | |||||||
| chr16:10761139 | C | T | 1 | a0004c0008t0002g0271 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.607-225C>T | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 7/10 | chr16 | 10761139 | |||||||
| chr16:10761484 | C | T | 65 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(62): Show |
123 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(120): Show |
intron_variant | MODIFIER | c.717+10C>T | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 8/10 | chr16 | 10761484 | |||||||
| chr16:10761500 | G | A | 1 | a0001c0001t0001g0207 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.717+26G>A | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 8/10 | chr16 | 10761500 | |||||||
| chr16:10761664 | CT | C | 16 | a0001c0001t0001g0016 a0001c0001t0001g0050 a0001c0001t0001g0064 others(13): Show |
20 | HG00099.hp1 HG01123.hp2 HG01175.hp1 others(17): Show |
intron_variant | MODIFIER | c.718-79delT | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr16 | 10761664 | ||||||
| chr16:10761877 | G | T | 6 | a0001c0001t0002g0051 a0001c0001t0002g0225 a0001c0001t0002g0226 others(3): Show |
9 | HG02257.hp1 HG02486.hp1 HG02965.hp2 others(6): Show |
intron_variant | MODIFIER | c.820+18G>T | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 9/10 | chr16 | 10761877 | |||||||
| chr16:10761882 | G | A | 65 | a0001c0001t0001g0075 a0001c0001t0001g0104 a0001c0001t0002g0002 others(62): Show |
97 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(94): Show |
intron_variant | MODIFIER | c.820+23G>A | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 9/10 | chr16 | 10761882 | |||||||
| chr16:10761919 | C | T | 1 | a0001c0001t0001g0021 | 3 | HG01168.hp1 HG01169.hp1 HG01358.hp1 |
intron_variant | MODIFIER | c.820+60C>T | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 9/10 | chr16 | 10761919 | |||||||
| chr16:10761936 | G | A | 2 | a0001c0001t0002g0097 a0001c0001t0002g0098 |
2 | NA18957.hp2 NA18984.hp2 |
intron_variant | MODIFIER | c.820+77G>A | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 9/10 | chr16 | 10761936 | |||||||
| chr16:10761948 | G | A | 2 | a0001c0001t0001g0259 a0001c0001t0001g0260 |
2 | HG02145.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.820+89G>A | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 9/10 | chr16 | 10761948 | |||||||
| chr16:10762023 | G | A | 11 | a0001c0001t0001g0259 a0001c0001t0001g0260 a0001c0001t0001g0263 others(8): Show |
14 | HG02145.hp2 HG02257.hp1 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.820+164G>A | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 9/10 | chr16 | 10762023 | |||||||
| chr16:10762034 | C | T | 3 | a0001c0001t0001g0216 a0001c0001t0001g0217 a0001c0001t0002g0264 |
3 | HG02055.hp2 HG02451.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.820+175C>T | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 9/10 | chr16 | 10762034 | |||||||
| chr16:10762055 | G | A | 1 | a0001c0001t0002g0228 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.820+196G>A | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 9/10 | chr16 | 10762055 | |||||||
| chr16:10762114 | G | A | 1 | a0002c0002t0001g0240 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.820+255G>A | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 9/10 | chr16 | 10762114 | |||||||
| chr16:10762143 | A | G | 1 | a0001c0001t0001g0145 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.820+284A>G | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 9/10 | chr16 | 10762143 | |||||||
| chr16:10762163 | G | A | 1 | a0001c0001t0001g0185 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.820+304G>A | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 9/10 | chr16 | 10762163 | |||||||
| chr16:10762242 | C | T | 1 | a0001c0001t0002g0118 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.820+383C>T | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 9/10 | chr16 | 10762242 | |||||||
| chr16:10762254 | G | T | 28 | a0001c0001t0001g0123 a0001c0001t0001g0258 a0001c0001t0002g0089 others(25): Show |
36 | HG00738.hp1 HG01070.hp1 HG01070.hp2 others(33): Show |
intron_variant | MODIFIER | c.820+395G>T | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 9/10 | chr16 | 10762254 | |||||||
| chr16:10762292 | C | A | 1 | a0001c0001t0001g0140 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.820+433C>A | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 9/10 | chr16 | 10762292 | |||||||
| chr16:10762330 | C | A | 53 | a0001c0001t0001g0075 a0001c0001t0001g0104 a0001c0001t0002g0002 others(50): Show |
82 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(79): Show |
intron_variant | MODIFIER | c.820+471C>A | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 9/10 | chr16 | 10762330 | |||||||
| chr16:10762460 | G | A | 1 | a0001c0001t0001g0129 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.820+601G>A | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 9/10 | chr16 | 10762460 | |||||||
| chr16:10762483 | C | T | 52 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0012 others(49): Show |
89 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(86): Show |
intron_variant | MODIFIER | c.820+624C>T | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 9/10 | chr16 | 10762483 | |||||||
| chr16:10762493 | G | A | 56 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0012 others(53): Show |
97 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(94): Show |
intron_variant | MODIFIER | c.820+634G>A | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 9/10 | chr16 | 10762493 | |||||||
| chr16:10762508 | C | T | 40 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0012 others(37): Show |
74 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(71): Show |
intron_variant | MODIFIER | c.820+649C>T | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 9/10 | chr16 | 10762508 | |||||||
| chr16:10762547 | G | A | 1 | a0001c0001t0002g0111 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.820+688G>A | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 9/10 | chr16 | 10762547 | |||||||
| chr16:10762581 | T | A | 1 | a0001c0001t0001g0153 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.820+722T>A | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 9/10 | chr16 | 10762581 | |||||||
| chr16:10762642 | A | G | 2 | a0001c0001t0005g0031 a0001c0001t0005g0059 |
3 | HG02630.hp2 HG02886.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.820+783A>G | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 9/10 | chr16 | 10762642 | |||||||
| chr16:10762678 | G | A | 44 | a0001c0001t0001g0006 a0001c0001t0001g0104 a0001c0001t0001g0154 others(41): Show |
63 | HG00423.hp1 HG00423.hp2 HG00558.hp2 others(60): Show |
intron_variant | MODIFIER | c.820+819G>A | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 9/10 | chr16 | 10762678 | |||||||
| chr16:10762728 | C | T | 21 | a0001c0001t0001g0010 a0001c0001t0001g0045 a0001c0001t0001g0133 others(18): Show |
30 | HG00544.hp1 HG01070.hp1 HG01071.hp2 others(27): Show |
intron_variant | MODIFIER | c.820+869C>T | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 9/10 | chr16 | 10762728 | |||||||
| chr16:10762835 | G | A | 1 | a0001c0001t0002g0085 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.820+976G>A | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 9/10 | chr16 | 10762835 | |||||||
| chr16:10762839 | A | AGAGCCTG others(28): Show |
1 | a0001c0001t0002g0093 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.820+987_820+1021du others(36): Show |
NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr16 | 10762839 | ||||||
| chr16:10762839 | A | AGAGCCTG others(63): Show |
1 | a0001c0001t0001g0155 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.820+1021_820+1022i others(72): Show |
NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr16 | 10762839 | ||||||
| chr16:10762931 | G | C | 1 | a0001c0001t0002g0229 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.820+1072G>C | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 9/10 | chr16 | 10762931 | |||||||
| chr16:10763015 | T | C | 1 | a0001c0001t0002g0068 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.820+1156T>C | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 9/10 | chr16 | 10763015 | |||||||
| chr16:10763111 | G | A | 1 | a0001c0001t0001g0037 | 2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.820+1252G>A | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 9/10 | chr16 | 10763111 | |||||||
| chr16:10763166 | G | A | 1 | a0001c0001t0001g0181 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.820+1307G>A | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 9/10 | chr16 | 10763166 | |||||||
| chr16:10763184 | G | A | 1 | a0001c0001t0001g0165 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.820+1325G>A | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 9/10 | chr16 | 10763184 | |||||||
| chr16:10763394 | C | G | 8 | a0001c0001t0002g0017 a0001c0001t0002g0055 a0001c0001t0002g0056 others(5): Show |
13 | HG01167.hp1 HG01169.hp2 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.820+1535C>G | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 9/10 | chr16 | 10763394 | |||||||
| chr16:10763394 | C | T | 1 | a0001c0001t0001g0201 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.820+1535C>T | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 9/10 | chr16 | 10763394 | |||||||
| chr16:10763466 | C | T | 1 | a0001c0001t0001g0200 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.820+1607C>T | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 9/10 | chr16 | 10763466 | |||||||
| chr16:10763514 | T | C | 8 | a0001c0001t0001g0142 a0001c0001t0003g0053 a0001c0001t0003g0054 others(5): Show |
11 | HG01106.hp1 HG02559.hp2 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.820+1655T>C | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 9/10 | chr16 | 10763514 | |||||||
| chr16:10763521 | G | A | 1 | a0001c0001t0002g0269 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.820+1662G>A | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 9/10 | chr16 | 10763521 | |||||||
| chr16:10763593 | G | C | 15 | a0001c0001t0001g0142 a0001c0001t0002g0051 a0001c0001t0002g0225 others(12): Show |
21 | HG01106.hp1 HG02257.hp1 HG02280.hp1 others(18): Show |
intron_variant | MODIFIER | c.820+1734G>C | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 9/10 | chr16 | 10763593 | |||||||
| chr16:10763622 | T | C | 4 | a0001c0001t0001g0195 a0001c0001t0002g0019 a0001c0001t0002g0033 others(1): Show |
7 | HG01192.hp2 HG01496.hp2 HG01978.hp2 others(4): Show |
intron_variant | MODIFIER | c.820+1763T>C | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 9/10 | chr16 | 10763622 | |||||||
| chr16:10763866 | G | A | 1 | a0002c0002t0001g0028 | 3 | HG02602.hp2 HG03704.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.820+2007G>A | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 9/10 | chr16 | 10763866 | |||||||
| chr16:10763975 | G | C | 1 | a0001c0001t0001g0166 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.820+2116G>C | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 9/10 | chr16 | 10763975 | |||||||
| chr16:10763975 | G | GCCACGGG others(137): Show |
1 | a0001c0001t0002g0261 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.820+2173_820+2174i others(146): Show |
NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr16 | 10763975 | ||||||
| chr16:10764052 | AGGAGCAT others(11): Show |
A | 2 | a0001c0001t0002g0119 a0001c0001t0002g0120 |
2 | HG01433.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.820+2202_820+2219d others(20): Show |
NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr16 | 10764052 | ||||||
| chr16:10764054 | G | A | 1 | a0001c0001t0001g0176 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.820+2195G>A | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 9/10 | chr16 | 10764054 | |||||||
| chr16:10764085 | C | G | 1 | a0001c0001t0001g0132 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.820+2226C>G | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 9/10 | chr16 | 10764085 | |||||||
| chr16:10764119 | C | G | 2 | a0001c0001t0002g0270 a0004c0008t0002g0271 |
2 | HG02572.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.820+2260C>G | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 9/10 | chr16 | 10764119 | |||||||
| chr16:10764177 | C | T | 3 | a0001c0001t0001g0136 a0001c0001t0001g0195 a0001c0001t0002g0071 |
3 | HG01081.hp2 NA18991.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.820+2318C>T | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 9/10 | chr16 | 10764177 | |||||||
| chr16:10764313 | G | A | 1 | a0001c0001t0002g0019 | 3 | HG01192.hp2 HG01496.hp2 HG03490.hp1 |
intron_variant | MODIFIER | c.820+2454G>A | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 9/10 | chr16 | 10764313 | |||||||
| chr16:10764485 | A | G | 2 | a0001c0001t0002g0270 a0004c0008t0002g0271 |
2 | HG02572.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.820+2626A>G | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 9/10 | chr16 | 10764485 | |||||||
| chr16:10764513 | T | G | 2 | a0001c0001t0002g0270 a0004c0008t0002g0271 |
2 | HG02572.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.820+2654T>G | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 9/10 | chr16 | 10764513 | |||||||
| chr16:10764519 | A | G | 2 | a0001c0001t0002g0270 a0004c0008t0002g0271 |
2 | HG02572.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.820+2660A>G | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 9/10 | chr16 | 10764519 | |||||||
| chr16:10764533 | T | G | 2 | a0001c0001t0002g0270 a0004c0008t0002g0271 |
2 | HG02572.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.820+2674T>G | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 9/10 | chr16 | 10764533 | |||||||
| chr16:10764547 | T | G | 2 | a0001c0001t0002g0270 a0004c0008t0002g0271 |
2 | HG02572.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.820+2688T>G | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 9/10 | chr16 | 10764547 | |||||||
| chr16:10764553 | A | G | 2 | a0001c0001t0002g0270 a0004c0008t0002g0271 |
2 | HG02572.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.820+2694A>G | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 9/10 | chr16 | 10764553 | |||||||
| chr16:10764589 | A | G | 2 | a0001c0001t0002g0270 a0004c0008t0002g0271 |
2 | HG02572.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.820+2730A>G | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 9/10 | chr16 | 10764589 | |||||||
| chr16:10764620 | A | AGTCTATT others(25): Show |
1 | a0001c0001t0002g0264 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.820+2792_820+2793i others(34): Show |
NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr16 | 10764620 | ||||||
| chr16:10764625 | A | G | 2 | a0001c0001t0002g0270 a0004c0008t0002g0271 |
2 | HG02572.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.820+2766A>G | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 9/10 | chr16 | 10764625 | |||||||
| chr16:10764659 | C | CTGTTGGA others(61): Show |
2 | a0001c0001t0002g0270 a0004c0008t0002g0271 |
2 | HG02572.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.820+2801_820+2802i others(70): Show |
NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr16 | 10764659 | ||||||
| chr16:10764661 | A | G | 3 | a0001c0001t0002g0264 a0001c0001t0002g0270 a0004c0008t0002g0271 |
3 | HG02451.hp2 HG02572.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.820+2802A>G | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 9/10 | chr16 | 10764661 | |||||||
| chr16:10764687 | A | ATGTC | 3 | a0001c0001t0002g0264 a0001c0001t0002g0270 a0004c0008t0002g0271 |
3 | HG02451.hp2 HG02572.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.820+2828_820+2829i others(6): Show |
NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 9/10 | chr16 | 10764687 | |||||||
| chr16:10764688 | G | A | 3 | a0001c0001t0002g0264 a0001c0001t0002g0270 a0004c0008t0002g0271 |
3 | HG02451.hp2 HG02572.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.820+2829G>A | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 9/10 | chr16 | 10764688 | |||||||
| chr16:10764693 | A | ATTGGAGC others(29): Show |
1 | a0001c0001t0001g0265 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.820+2954_820+2989d others(38): Show |
NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr16 | 10764693 | ||||||
| chr16:10764693 | A | ATTGGAGC others(313): Show |
7 | a0001c0001t0003g0053 a0001c0001t0003g0054 a0001c0001t0003g0057 others(4): Show |
10 | HG01106.hp1 HG02559.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.820+2905_820+2906i others(322): Show |
NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr16 | 10764693 | ||||||
| chr16:10764693 | A | ATTGGAGC others(349): Show |
6 | a0001c0001t0002g0051 a0001c0001t0002g0225 a0001c0001t0002g0226 others(3): Show |
9 | HG02257.hp1 HG02486.hp1 HG02965.hp2 others(6): Show |
intron_variant | MODIFIER | c.820+2905_820+2906i others(358): Show |
NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr16 | 10764693 | ||||||
| chr16:10764693 | A | G | 3 | a0001c0001t0002g0264 a0001c0001t0002g0270 a0004c0008t0002g0271 |
3 | HG02451.hp2 HG02572.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.820+2834A>G | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 9/10 | chr16 | 10764693 | |||||||
| chr16:10764693 | ATTGGAGC others(29): Show |
A | 1 | a0001c0001t0001g0199 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.820+2954_820+2989d others(38): Show |
NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr16 | 10764693 | ||||||
| chr16:10764709 | C | T | 1 | a0002c0002t0001g0244 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.820+2850C>T | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 9/10 | chr16 | 10764709 | |||||||
| chr16:10764729 | G | GTTGGAGC others(133): Show |
1 | a0001c0001t0002g0269 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.820+2905_820+2906i others(142): Show |
NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr16 | 10764729 | ||||||
| chr16:10764742 | AGTCTGCT others(99): Show |
A | 87 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(84): Show |
147 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(144): Show |
intron_variant | MODIFIER | c.820+2954_821-3031d others(2): Show |
NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr16 | 10764742 | ||||||
| chr16:10764778 | AGTCTGCT others(63): Show |
A | 2 | a0001c0001t0001g0138 a0001c0001t0001g0263 |
2 | HG02258.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.820+3002_821-3019d others(72): Show |
NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr16 | 10764778 | ||||||
| chr16:10764848 | T | TCA | 35 | a0001c0001t0001g0136 a0001c0001t0002g0051 a0001c0001t0002g0225 others(32): Show |
48 | HG00738.hp1 HG01070.hp1 HG01070.hp2 others(45): Show |
intron_variant | MODIFIER | c.820+2989_820+2990i others(4): Show |
NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 9/10 | chr16 | 10764848 | |||||||
| chr16:10764848 | T | TCAGTCTG others(99): Show |
1 | a0001c0001t0002g0230 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.820+2989_820+2990i others(108): Show |
NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 9/10 | chr16 | 10764848 | |||||||
| chr16:10764848 | T | TCAGTCTG others(135): Show |
78 | a0001c0001t0001g0072 a0001c0001t0002g0002 a0001c0001t0002g0008 others(75): Show |
112 | HG00323.hp1 HG00423.hp1 HG00438.hp1 others(109): Show |
intron_variant | MODIFIER | c.820+2989_820+2990i others(144): Show |
NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 9/10 | chr16 | 10764848 | |||||||
| chr16:10764945 | C | T | 86 | a0001c0001t0001g0072 a0001c0001t0002g0002 a0001c0001t0002g0008 others(83): Show |
123 | HG00323.hp1 HG00423.hp1 HG00438.hp1 others(120): Show |
intron_variant | MODIFIER | c.821-3004C>T | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 9/10 | chr16 | 10764945 | |||||||
| chr16:10765097 | G | A | 1 | a0001c0001t0001g0182 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.821-2852G>A | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 9/10 | chr16 | 10765097 | |||||||
| chr16:10765168 | T | C | 1 | a0001c0001t0002g0269 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.821-2781T>C | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 9/10 | chr16 | 10765168 | |||||||
| chr16:10765262 | T | TAC | 16 | a0001c0001t0001g0016 a0001c0001t0001g0123 a0001c0001t0001g0185 others(13): Show |
22 | HG00673.hp2 HG01106.hp1 HG01255.hp2 others(19): Show |
intron_variant | MODIFIER | c.821-2667_821-2666d others(4): Show |
NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr16 | 10765262 | ||||||
| chr16:10765272 | C | G | 2 | a0001c0001t0002g0270 a0004c0008t0002g0271 |
2 | HG02572.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.821-2677C>G | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 9/10 | chr16 | 10765272 | |||||||
| chr16:10765327 | T | TA | 88 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(85): Show |
147 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(144): Show |
intron_variant | MODIFIER | c.821-2600dupA | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr16 | 10765327 | ||||||
| chr16:10765327 | TA | T | 17 | a0001c0001t0001g0048 a0001c0001t0001g0132 a0001c0001t0001g0188 others(14): Show |
18 | HG01071.hp1 HG01515.hp2 HG01516.hp2 others(15): Show |
intron_variant | MODIFIER | c.821-2600delA | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr16 | 10765327 | ||||||
| chr16:10765327 | TAA | T | 18 | a0001c0001t0002g0051 a0001c0001t0002g0098 a0001c0001t0002g0225 others(15): Show |
24 | HG01106.hp1 HG02257.hp1 HG02486.hp1 others(21): Show |
intron_variant | MODIFIER | c.821-2601_821-2600d others(4): Show |
NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr16 | 10765327 | ||||||
| chr16:10765327 | TAAA | T | 12 | a0001c0001t0001g0136 a0002c0002t0001g0027 a0002c0002t0001g0028 others(9): Show |
18 | HG00738.hp1 HG01070.hp2 HG01081.hp2 others(15): Show |
intron_variant | MODIFIER | c.821-2602_821-2600d others(5): Show |
NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr16 | 10765327 | ||||||
| chr16:10765466 | C | G | 2 | a0001c0001t0002g0254 a0001c0001t0002g0256 |
2 | HG02280.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.821-2483C>G | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 9/10 | chr16 | 10765466 | |||||||
| chr16:10765508 | A | C | 190 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(187): Show |
292 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(289): Show |
intron_variant | MODIFIER | c.821-2441A>C | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 9/10 | chr16 | 10765508 | |||||||
| chr16:10765520 | A | T | 5 | a0001c0001t0002g0222 a0001c0001t0002g0228 a0001c0001t0002g0229 others(2): Show |
5 | HG02109.hp2 HG02486.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.821-2429A>T | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 9/10 | chr16 | 10765520 | |||||||
| chr16:10765524 | A | G | 7 | a0001c0001t0003g0053 a0001c0001t0003g0054 a0001c0001t0003g0057 others(4): Show |
10 | HG01106.hp1 HG02559.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.821-2425A>G | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 9/10 | chr16 | 10765524 | |||||||
| chr16:10765635 | G | A | 1 | a0002c0002t0001g0248 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.821-2314G>A | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 9/10 | chr16 | 10765635 | |||||||
| chr16:10765755 | G | C | 80 | a0001c0001t0001g0072 a0001c0001t0001g0130 a0001c0001t0002g0002 others(77): Show |
114 | HG00323.hp1 HG00423.hp1 HG00438.hp1 others(111): Show |
intron_variant | MODIFIER | c.821-2194G>C | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 9/10 | chr16 | 10765755 | |||||||
| chr16:10765843 | G | A | 13 | a0001c0001t0002g0051 a0001c0001t0002g0225 a0001c0001t0002g0226 others(10): Show |
19 | HG01106.hp1 HG02257.hp1 HG02486.hp1 others(16): Show |
intron_variant | MODIFIER | c.821-2106G>A | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 9/10 | chr16 | 10765843 | |||||||
| chr16:10765951 | C | G | 1 | a0001c0001t0001g0157 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.821-1998C>G | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 9/10 | chr16 | 10765951 | |||||||
| chr16:10766063 | T | A | 2 | a0001c0001t0001g0190 a0001c0001t0001g0192 |
2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.821-1886T>A | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 9/10 | chr16 | 10766063 | |||||||
| chr16:10766091 | G | T | 71 | a0001c0001t0002g0002 a0001c0001t0002g0008 a0001c0001t0002g0009 others(68): Show |
104 | HG00323.hp1 HG00423.hp1 HG00438.hp1 others(101): Show |
intron_variant | MODIFIER | c.821-1858G>T | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 9/10 | chr16 | 10766091 | |||||||
| chr16:10766449 | G | C | 3 | a0001c0001t0001g0075 a0001c0001t0001g0076 a0001c0001t0001g0128 |
3 | HG00280.hp1 HG00280.hp2 HG00642.hp2 |
intron_variant | MODIFIER | c.821-1500G>C | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 9/10 | chr16 | 10766449 | |||||||
| chr16:10766554 | G | T | 2 | a0001c0001t0002g0095 a0001c0001t0002g0107 |
2 | NA18747.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.821-1395G>T | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 9/10 | chr16 | 10766554 | |||||||
| chr16:10766578 | C | T | 1 | a0001c0001t0001g0183 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.821-1371C>T | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 9/10 | chr16 | 10766578 | |||||||
| chr16:10766689 | A | G | 2 | a0001c0001t0002g0270 a0004c0008t0002g0271 |
2 | HG02572.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.821-1260A>G | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 9/10 | chr16 | 10766689 | |||||||
| chr16:10766722 | G | C | 79 | a0001c0001t0001g0130 a0001c0001t0002g0002 a0001c0001t0002g0008 others(76): Show |
113 | HG00323.hp1 HG00423.hp1 HG00438.hp1 others(110): Show |
intron_variant | MODIFIER | c.821-1227G>C | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 9/10 | chr16 | 10766722 | |||||||
| chr16:10766762 | G | T | 1 | a0001c0001t0001g0203 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.821-1187G>T | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 9/10 | chr16 | 10766762 | |||||||
| chr16:10766788 | A | G | 6 | a0001c0001t0002g0051 a0001c0001t0002g0225 a0001c0001t0002g0226 others(3): Show |
9 | HG02257.hp1 HG02486.hp1 HG02965.hp2 others(6): Show |
intron_variant | MODIFIER | c.821-1161A>G | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 9/10 | chr16 | 10766788 | |||||||
| chr16:10766808 | C | T | 21 | a0001c0001t0001g0001 a0001c0001t0001g0021 a0001c0001t0001g0022 others(18): Show |
45 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(42): Show |
intron_variant | MODIFIER | c.821-1141C>T | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 9/10 | chr16 | 10766808 | |||||||
| chr16:10766902 | G | A | 1 | a0001c0001t0001g0134 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.821-1047G>A | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 9/10 | chr16 | 10766902 | |||||||
| chr16:10766927 | T | G | 1 | a0001c0001t0001g0167 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.821-1022T>G | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 9/10 | chr16 | 10766927 | |||||||
| chr16:10767196 | G | A | 1 | a0001c0001t0002g0269 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.821-753G>A | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 9/10 | chr16 | 10767196 | |||||||
| chr16:10767253 | C | T | 49 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(46): Show |
99 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(96): Show |
intron_variant | MODIFIER | c.821-696C>T | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 9/10 | chr16 | 10767253 | |||||||
| chr16:10767401 | A | G | 80 | a0001c0001t0001g0072 a0001c0001t0002g0002 a0001c0001t0002g0008 others(77): Show |
114 | HG00323.hp1 HG00423.hp1 HG00438.hp1 others(111): Show |
intron_variant | MODIFIER | c.821-548A>G | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 9/10 | chr16 | 10767401 | |||||||
| chr16:10767452 | T | C | 1 | a0001c0001t0001g0185 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.821-497T>C | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 9/10 | chr16 | 10767452 | |||||||
| chr16:10767483 | TGC | T | 72 | a0001c0001t0001g0072 a0001c0001t0002g0002 a0001c0001t0002g0008 others(69): Show |
105 | HG00323.hp1 HG00423.hp1 HG00438.hp1 others(102): Show |
intron_variant | MODIFIER | c.821-463_821-462del others(2): Show |
NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr16 | 10767483 | ||||||
| chr16:10767485 | C | T | 31 | a0001c0001t0002g0017 a0001c0001t0002g0051 a0001c0001t0002g0055 others(28): Show |
43 | HG01106.hp1 HG01167.hp1 HG01169.hp2 others(40): Show |
intron_variant | MODIFIER | c.821-464C>T | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 9/10 | chr16 | 10767485 | |||||||
| chr16:10767626 | A | T | 6 | a0001c0001t0002g0051 a0001c0001t0002g0225 a0001c0001t0002g0226 others(3): Show |
9 | HG02257.hp1 HG02486.hp1 HG02965.hp2 others(6): Show |
intron_variant | MODIFIER | c.821-323A>T | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 9/10 | chr16 | 10767626 | |||||||
| chr16:10767842 | G | A | 1 | a0002c0002t0001g0245 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.821-107G>A | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 9/10 | chr16 | 10767842 | |||||||
| chr16:10767859 | T | C | 18 | a0001c0001t0002g0017 a0001c0001t0002g0055 a0001c0001t0002g0056 others(15): Show |
26 | HG01106.hp1 HG01167.hp1 HG01169.hp2 others(23): Show |
intron_variant | MODIFIER | c.821-90T>C | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 9/10 | chr16 | 10767859 | |||||||
| chr16:10768057 | T | C | 104 | a0001c0001t0001g0072 a0001c0001t0001g0133 a0001c0001t0002g0002 others(101): Show |
149 | HG00323.hp1 HG00423.hp1 HG00438.hp1 others(146): Show |
intron_variant | MODIFIER | c.904+25T>C | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 10/10 | chr16 | 10768057 | |||||||
| chr16:10768098 | G | A | 1 | a0001c0001t0001g0143 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.904+66G>A | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 10/10 | chr16 | 10768098 | |||||||
| chr16:10768206 | G | C | 1 | a0001c0001t0001g0178 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.904+174G>C | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 10/10 | chr16 | 10768206 | |||||||
| chr16:10768308 | T | TA | 19 | a0001c0001t0001g0136 a0001c0001t0001g0156 a0001c0001t0001g0203 others(16): Show |
26 | HG00639.hp2 HG00738.hp1 HG01070.hp1 others(23): Show |
intron_variant | MODIFIER | c.904+288dupA | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr16 | 10768308 | ||||||
| chr16:10768308 | TA | T | 101 | a0001c0001t0002g0002 a0001c0001t0002g0008 a0001c0001t0002g0009 others(98): Show |
146 | HG00323.hp1 HG00423.hp1 HG00438.hp1 others(143): Show |
intron_variant | MODIFIER | c.904+288delA | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr16 | 10768308 | ||||||
| chr16:10768362 | G | A | 1 | a0001c0001t0001g0168 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.904+330G>A | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 10/10 | chr16 | 10768362 | |||||||
| chr16:10768374 | A | C | 80 | a0001c0001t0001g0072 a0001c0001t0002g0002 a0001c0001t0002g0008 others(77): Show |
114 | HG00323.hp1 HG00423.hp1 HG00438.hp1 others(111): Show |
intron_variant | MODIFIER | c.904+342A>C | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 10/10 | chr16 | 10768374 | |||||||
| chr16:10768399 | G | C | 1 | a0001c0001t0002g0055 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.904+367G>C | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 10/10 | chr16 | 10768399 | |||||||
| chr16:10768496 | A | G | 89 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(86): Show |
149 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(146): Show |
intron_variant | MODIFIER | c.904+464A>G | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 10/10 | chr16 | 10768496 | |||||||
| chr16:10768538 | C | T | 1 | a0001c0001t0001g0169 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.904+506C>T | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 10/10 | chr16 | 10768538 | |||||||
| chr16:10768600 | G | A | 1 | a0001c0001t0002g0264 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.905-447G>A | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 10/10 | chr16 | 10768600 | |||||||
| chr16:10768745 | A | G | 7 | a0001c0001t0001g0021 a0001c0001t0001g0037 a0001c0001t0001g0126 others(4): Show |
10 | HG00140.hp1 HG01168.hp1 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.905-302A>G | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 10/10 | chr16 | 10768745 | |||||||
| chr16:10768840 | G | T | 2 | a0001c0001t0001g0038 a0001c0001t0001g0129 |
3 | HG00438.hp2 NA18962.hp2 NA18964.hp1 |
intron_variant | MODIFIER | c.905-207G>T | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 10/10 | chr16 | 10768840 | |||||||
| chr16:10768850 | C | T | 103 | a0001c0001t0001g0188 a0001c0001t0002g0002 a0001c0001t0002g0008 others(100): Show |
148 | HG00323.hp1 HG00423.hp1 HG00438.hp1 others(145): Show |
intron_variant | MODIFIER | c.905-197C>T | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 10/10 | chr16 | 10768850 | |||||||
| chr16:10769022 | C | G | 4 | a0001c0001t0003g0053 a0001c0001t0003g0054 a0001c0001t0003g0057 others(1): Show |
7 | HG02559.hp2 HG02615.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.905-25C>G | NUBP1 | ENSG00000103274.11 | transcript | ENST00000283027.10 | protein_coding | 10/10 | chr16 | 10769022 |