Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 4086 |
| ensemblid | ENSG00000170365.10 |
| hgncid | 6767 |
| symbol | SMAD1 |
| name | SMAD family member 1 |
| refseq_nuc | NM_005900.3 |
| refseq_prot | NP_005891.1 |
| ensembl_nuc | ENST00000302085.9 |
| ensembl_prot | ENSP00000305769.4 |
| mane_status | MANE Select |
| chr | chr4 |
| start | 145481853 |
| end | 145559176 |
| strand | + |
| ver | v1.2 |
| region | chr4:145481853-145559176 |
| region5000 | chr4:145476853-145564176 |
| regionname0 | SMAD1_chr4_145481853_145559176 |
| regionname5000 | SMAD1_chr4_145476853_145564176 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 465 | 307 | 90 | 56 | 111 | 12 | 36 | 77 | SMAD1_chr4_145476853_145564176 | SMAD1 | MNVTS others(460): Show |
chr4 | 145476853 | 145564176 |
| a0002 | 0/0 | 465 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SMAD1_chr4_145476853_145564176 | SMAD1 | MNVTS others(460): Show |
chr4 | 145476853 | 145564176 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1395 | 301 | 84 | 56 | 111 | 12 | 36 | SMAD1_chr4_145476853_145564176 | SMAD1 | ATGAA others(1390): Show |
chr4 | 145476853 | 145564176 | ||
| a0001c0002 | 0/0 | 1395 | 4 | 4 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | ATGAA others(1390): Show |
chr4 | 145476853 | 145564176 | ||
| a0001c0003 | 0/0 | 1395 | 2 | 2 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | ATGAA others(1390): Show |
chr4 | 145476853 | 145564176 | ||
| a0002c0004 | 0/0 | 1395 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | ATGAA others(1390): Show |
chr4 | 145476853 | 145564176 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 3002 | 72 | 29 | 12 | 17 | 5 | 9 | SMAD1_chr4_145476853_145564176 | SMAD1 | AGATC others(2997): Show |
chr4 | 145476853 | 145564176 |
| a0001c0001t0002 | 1/0 | 3002 | 64 | 0 | 14 | 43 | 3 | 3 | SMAD1_chr4_145476853_145564176 | SMAD1 | AGATC others(2997): Show |
chr4 | 145476853 | 145564176 |
| a0001c0001t0003 | 0/0 | 3005 | 38 | 1 | 13 | 16 | 3 | 5 | SMAD1_chr4_145476853_145564176 | SMAD1 | AGATC others(3000): Show |
chr4 | 145476853 | 145564176 |
| a0001c0001t0004 | 0/0 | 3003 | 34 | 12 | 2 | 13 | 0 | 7 | SMAD1_chr4_145476853_145564176 | SMAD1 | AGATC others(2998): Show |
chr4 | 145476853 | 145564176 |
| a0001c0001t0005 | 0/0 | 3004 | 17 | 7 | 1 | 9 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | AGATC others(2999): Show |
chr4 | 145476853 | 145564176 |
| a0001c0001t0006 | 0/0 | 3004 | 10 | 0 | 2 | 5 | 1 | 2 | SMAD1_chr4_145476853_145564176 | SMAD1 | AGATC others(2999): Show |
chr4 | 145476853 | 145564176 |
| a0001c0001t0007 | 0/0 | 3004 | 9 | 2 | 1 | 6 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | AGATC others(2999): Show |
chr4 | 145476853 | 145564176 |
| a0001c0001t0008 | 0/0 | 3004 | 8 | 6 | 2 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | AGATC others(2999): Show |
chr4 | 145476853 | 145564176 |
| a0001c0001t0009 | 0/0 | 3004 | 7 | 6 | 1 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | AGATC others(2999): Show |
chr4 | 145476853 | 145564176 |
| a0001c0001t0010 | 0/0 | 3003 | 6 | 3 | 3 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | AGATC others(2998): Show |
chr4 | 145476853 | 145564176 |
| a0001c0001t0011 | 0/0 | 3004 | 5 | 5 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | AGATC others(2999): Show |
chr4 | 145476853 | 145564176 |
| a0001c0001t0013 | 0/0 | 3004 | 4 | 0 | 0 | 0 | 0 | 4 | SMAD1_chr4_145476853_145564176 | SMAD1 | AGATC others(2999): Show |
chr4 | 145476853 | 145564176 |
| a0001c0001t0014 | 0/0 | 3005 | 3 | 3 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | AGATC others(3000): Show |
chr4 | 145476853 | 145564176 |
| a0001c0001t0015 | 0/0 | 3005 | 3 | 3 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | AGATC others(3000): Show |
chr4 | 145476853 | 145564176 |
| a0001c0001t0016 | 0/0 | 3003 | 2 | 1 | 1 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | AGATC others(2998): Show |
chr4 | 145476853 | 145564176 |
| a0001c0001t0017 | 0/0 | 3005 | 2 | 0 | 0 | 1 | 0 | 1 | SMAD1_chr4_145476853_145564176 | SMAD1 | AGATC others(3000): Show |
chr4 | 145476853 | 145564176 |
| a0001c0001t0018 | 0/0 | 3004 | 2 | 2 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | AGATC others(2999): Show |
chr4 | 145476853 | 145564176 |
| a0001c0001t0019 | 0/0 | 3004 | 2 | 2 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | AGATC others(2999): Show |
chr4 | 145476853 | 145564176 |
| a0001c0001t0020 | 0/0 | 3005 | 2 | 0 | 2 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | AGATC others(3000): Show |
chr4 | 145476853 | 145564176 |
| a0001c0001t0021 | 0/0 | 3005 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | AGATC others(3000): Show |
chr4 | 145476853 | 145564176 |
| a0001c0001t0022 | 0/0 | 3002 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | AGATC others(2997): Show |
chr4 | 145476853 | 145564176 |
| a0001c0001t0023 | 0/0 | 3003 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD1_chr4_145476853_145564176 | SMAD1 | AGATC others(2998): Show |
chr4 | 145476853 | 145564176 |
| a0001c0001t0024 | 0/1 | 3005 | 1 | 0 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | AGATC others(3000): Show |
chr4 | 145476853 | 145564176 |
| a0001c0001t0025 | 0/0 | 3005 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD1_chr4_145476853_145564176 | SMAD1 | AGATC others(3000): Show |
chr4 | 145476853 | 145564176 |
| a0001c0001t0026 | 0/0 | 3003 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | AGATC others(2998): Show |
chr4 | 145476853 | 145564176 |
| a0001c0001t0027 | 0/0 | 3005 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | AGATC others(3000): Show |
chr4 | 145476853 | 145564176 |
| a0001c0001t0028 | 0/0 | 3005 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD1_chr4_145476853_145564176 | SMAD1 | AGATC others(3000): Show |
chr4 | 145476853 | 145564176 |
| a0001c0001t0029 | 0/0 | 3004 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD1_chr4_145476853_145564176 | SMAD1 | AGATC others(2999): Show |
chr4 | 145476853 | 145564176 |
| a0001c0001t0031 | 0/0 | 3002 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | AGATC others(2997): Show |
chr4 | 145476853 | 145564176 |
| a0001c0001t0032 | 0/0 | 3005 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD1_chr4_145476853_145564176 | SMAD1 | AGATC others(3000): Show |
chr4 | 145476853 | 145564176 |
| a0001c0002t0012 | 0/0 | 3004 | 3 | 3 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | AGATC others(2999): Show |
chr4 | 145476853 | 145564176 |
| a0001c0002t0030 | 0/0 | 3002 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | AGATC others(2997): Show |
chr4 | 145476853 | 145564176 |
| a0001c0003t0012 | 0/0 | 3004 | 2 | 2 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | AGATC others(2999): Show |
chr4 | 145476853 | 145564176 |
| a0002c0004t0002 | 0/0 | 3002 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | AGATC others(2997): Show |
chr4 | 145476853 | 145564176 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0003 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| a0001c0001t0001g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| a0001c0001t0001g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| a0001c0001t0001g0021 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| a0001c0001t0001g0022 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| a0001c0001t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| a0001c0001t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| a0001c0001t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| a0001c0001t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| a0001c0001t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| a0001c0001t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| a0001c0001t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| a0001c0001t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| a0001c0001t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| a0001c0001t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| a0001c0001t0002g0001 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| a0001c0001t0002g0002 | 0/0 | 4 | 0 | 3 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| a0001c0001t0002g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| a0001c0001t0002g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| a0001c0001t0002g0015 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| a0001c0001t0002g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| a0001c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| a0001c0001t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| a0001c0001t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| a0001c0001t0002g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| a0001c0001t0002g0086 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| a0001c0001t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| a0001c0001t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| a0001c0001t0002g0089 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| a0001c0001t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| a0001c0001t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| a0001c0001t0002g0096 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| a0001c0001t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| a0001c0001t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| a0001c0001t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| a0001c0001t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| a0001c0001t0002g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| a0001c0001t0002g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| a0001c0001t0002g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| a0001c0001t0002g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| a0001c0001t0002g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| a0001c0001t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| a0001c0001t0002g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| a0001c0001t0002g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| a0001c0001t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| a0001c0001t0002g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| a0001c0001t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| a0001c0001t0002g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| a0001c0001t0002g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| a0001c0001t0002g0180 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| a0001c0001t0002g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| a0001c0001t0002g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| a0001c0001t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| a0001c0001t0002g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| a0001c0001t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| a0001c0001t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| a0001c0001t0002g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| a0001c0001t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| a0001c0001t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| a0001c0001t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| a0001c0001t0002g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| a0001c0001t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| a0001c0001t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| a0001c0001t0002g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| a0001c0001t0002g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| a0001c0001t0002g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| a0001c0001t0002g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| a0001c0001t0002g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| a0001c0001t0002g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| a0001c0001t0003g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| a0001c0001t0003g0016 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| a0001c0001t0003g0018 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| a0001c0001t0003g0019 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| a0001c0001t0003g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| a0001c0001t0003g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| a0001c0001t0003g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| a0001c0001t0003g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| a0001c0001t0003g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| a0001c0001t0003g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| a0001c0001t0003g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| a0001c0001t0003g0134 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| a0001c0001t0003g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| a0001c0001t0003g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| a0001c0001t0003g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| a0001c0001t0003g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| a0001c0001t0003g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| a0001c0001t0003g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| a0001c0001t0003g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| a0001c0001t0003g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| a0001c0001t0003g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| a0001c0001t0003g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| a0001c0001t0003g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| a0001c0001t0003g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| a0001c0001t0003g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| a0001c0001t0003g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| a0001c0001t0003g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| a0001c0001t0003g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| a0001c0001t0003g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| a0001c0001t0003g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| a0001c0001t0003g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| a0001c0001t0003g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| a0001c0001t0003g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| a0001c0001t0003g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| a0001c0001t0004g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| a0001c0001t0004g0008 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| a0001c0001t0004g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| a0001c0001t0004g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| a0001c0001t0004g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| a0001c0001t0004g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| a0001c0001t0004g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| a0001c0001t0004g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| a0001c0001t0004g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| a0001c0001t0004g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| a0001c0001t0004g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| a0001c0001t0004g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| a0001c0001t0004g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| a0001c0001t0004g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| a0001c0001t0004g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| a0001c0001t0004g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| a0001c0001t0004g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| a0001c0001t0004g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| a0001c0001t0004g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| a0001c0001t0004g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| a0001c0001t0004g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| a0001c0001t0004g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| a0001c0001t0004g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| a0001c0001t0004g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| a0001c0001t0004g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| a0001c0001t0004g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| a0001c0001t0004g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| a0001c0001t0004g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| a0001c0001t0004g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| a0001c0001t0004g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| a0001c0001t0004g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| a0001c0001t0005g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| a0001c0001t0005g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| a0001c0001t0005g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| a0001c0001t0005g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| a0001c0001t0005g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| a0001c0001t0005g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| a0001c0001t0005g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| a0001c0001t0005g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| a0001c0001t0005g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| a0001c0001t0005g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| a0001c0001t0005g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| a0001c0001t0005g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| a0001c0001t0005g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| a0001c0001t0005g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| a0001c0001t0005g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| a0001c0001t0005g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| a0001c0001t0005g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| a0001c0001t0006g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| a0001c0001t0006g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| a0001c0001t0006g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| a0001c0001t0006g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| a0001c0001t0006g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| a0001c0001t0006g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| a0001c0001t0006g0217 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| a0001c0001t0006g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| a0001c0001t0006g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| a0001c0001t0006g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| a0001c0001t0007g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| a0001c0001t0007g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| a0001c0001t0007g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| a0001c0001t0007g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| a0001c0001t0007g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| a0001c0001t0007g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| a0001c0001t0007g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| a0001c0001t0007g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| a0001c0001t0007g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| a0001c0001t0008g0020 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| a0001c0001t0008g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| a0001c0001t0008g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| a0001c0001t0008g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| a0001c0001t0008g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| a0001c0001t0008g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| a0001c0001t0008g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| a0001c0001t0009g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| a0001c0001t0009g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| a0001c0001t0009g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| a0001c0001t0009g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| a0001c0001t0009g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| a0001c0001t0009g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| a0001c0001t0010g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| a0001c0001t0010g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| a0001c0001t0010g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| a0001c0001t0010g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| a0001c0001t0010g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| a0001c0001t0011g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| a0001c0001t0011g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| a0001c0001t0011g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| a0001c0001t0011g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| a0001c0001t0013g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| a0001c0001t0013g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| a0001c0001t0013g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| a0001c0001t0013g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| a0001c0001t0014g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| a0001c0001t0014g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| a0001c0001t0014g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| a0001c0001t0015g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| a0001c0001t0015g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| a0001c0001t0016g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| a0001c0001t0016g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| a0001c0001t0017g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| a0001c0001t0017g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| a0001c0001t0018g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| a0001c0001t0018g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| a0001c0001t0019g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| a0001c0001t0019g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| a0001c0001t0020g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| a0001c0001t0020g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| a0001c0001t0021g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| a0001c0001t0022g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| a0001c0001t0023g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| a0001c0001t0024g0226 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| a0001c0001t0025g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| a0001c0001t0026g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| a0001c0001t0027g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| a0001c0001t0028g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| a0001c0001t0029g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| a0001c0001t0031g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| a0001c0001t0032g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| a0001c0002t0012g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| a0001c0002t0012g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| a0001c0002t0012g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| a0001c0002t0030g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| a0001c0003t0012g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| a0001c0003t0012g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| a0002c0004t0002g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0003 | g0019 | EUR | GBR | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| HG00099 | hp2 | a0001 | c0001 | t0002 | g0096 | EUR | GBR | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0259 | EUR | GBR | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| HG00140 | hp2 | a0001 | c0001 | t0002 | g0086 | EUR | GBR | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| HG00408 | hp1 | a0001 | c0001 | t0003 | g0004 | EAS | CHS | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| HG00408 | hp2 | a0001 | c0001 | t0002 | g0169 | EAS | CHS | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| HG00423 | hp1 | a0001 | c0001 | t0002 | g0196 | EAS | CHS | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| HG00423 | hp2 | a0001 | c0001 | t0004 | g0110 | EAS | CHS | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| HG00438 | hp1 | a0001 | c0001 | t0005 | g0046 | EAS | CHS | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| HG00438 | hp2 | a0001 | c0001 | t0021 | g0207 | EAS | CHS | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | CHS | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| HG00544 | hp2 | a0001 | c0001 | t0002 | g0191 | EAS | CHS | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| HG00558 | hp1 | a0001 | c0001 | t0002 | g0088 | EAS | CHS | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| HG00558 | hp2 | a0001 | c0001 | t0002 | g0195 | EAS | CHS | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| HG00597 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | CHS | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| HG00597 | hp2 | a0001 | c0001 | t0003 | g0004 | EAS | CHS | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| HG00609 | hp1 | a0001 | c0001 | t0003 | g0234 | EAS | CHS | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| HG00609 | hp2 | a0001 | c0001 | t0003 | g0093 | EAS | CHS | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| HG00621 | hp1 | a0001 | c0001 | t0004 | g0114 | EAS | CHS | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| HG00621 | hp2 | a0001 | c0001 | t0003 | g0255 | EAS | CHS | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| HG00639 | hp1 | a0001 | c0001 | t0002 | g0085 | AMR | PUR | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| HG00639 | hp2 | a0001 | c0001 | t0003 | g0131 | AMR | PUR | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| HG00642 | hp1 | a0001 | c0001 | t0003 | g0018 | AMR | PUR | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| HG00642 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| HG00673 | hp1 | a0001 | c0001 | t0002 | g0274 | EAS | CHS | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| HG00673 | hp2 | a0001 | c0001 | t0002 | g0087 | EAS | CHS | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0258 | AMR | PUR | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| HG00735 | hp2 | a0001 | c0001 | t0003 | g0019 | AMR | PUR | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| HG00738 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| HG00738 | hp2 | a0001 | c0001 | t0006 | g0213 | AMR | PUR | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| HG01069 | hp1 | a0001 | c0001 | t0003 | g0129 | AMR | PUR | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| HG01069 | hp2 | a0001 | c0001 | t0002 | g0164 | AMR | PUR | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0211 | AMR | PUR | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| HG01070 | hp2 | a0001 | c0001 | t0020 | g0128 | AMR | PUR | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0108 | AMR | PUR | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| HG01071 | hp2 | a0001 | c0001 | t0003 | g0238 | AMR | PUR | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0141 | AMR | PUR | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| HG01081 | hp2 | a0001 | c0001 | t0006 | g0218 | AMR | PUR | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| HG01099 | hp1 | a0001 | c0001 | t0003 | g0016 | AMR | PUR | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| HG01099 | hp2 | a0001 | c0001 | t0002 | g0189 | AMR | PUR | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| HG01106 | hp1 | a0001 | c0001 | t0003 | g0235 | AMR | PUR | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0210 | AMR | PUR | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| HG01167 | hp1 | a0001 | c0001 | t0002 | g0065 | AMR | PUR | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| HG01167 | hp2 | a0001 | c0001 | t0010 | g0132 | AMR | PUR | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| HG01169 | hp1 | a0001 | c0001 | t0016 | g0275 | AMR | PUR | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| HG01169 | hp2 | a0001 | c0001 | t0010 | g0245 | AMR | PUR | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| HG01175 | hp1 | a0001 | c0001 | t0004 | g0109 | AMR | PUR | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| HG01175 | hp2 | a0001 | c0001 | t0003 | g0252 | AMR | PUR | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| HG01192 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| HG01192 | hp2 | a0001 | c0001 | t0008 | g0256 | AMR | PUR | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| HG01243 | hp1 | a0001 | c0001 | t0004 | g0152 | AMR | PUR | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| HG01243 | hp2 | a0001 | c0001 | t0005 | g0026 | AMR | PUR | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0268 | AMR | CLM | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| HG01255 | hp2 | a0001 | c0001 | t0003 | g0016 | AMR | CLM | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| HG01257 | hp1 | a0001 | c0001 | t0003 | g0135 | AMR | CLM | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0094 | AMR | CLM | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| HG01261 | hp1 | a0001 | c0001 | t0009 | g0154 | AMR | CLM | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| HG01261 | hp2 | a0001 | c0001 | t0002 | g0179 | AMR | CLM | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| HG01358 | hp1 | a0001 | c0001 | t0002 | g0178 | AMR | CLM | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| HG01358 | hp2 | a0001 | c0001 | t0003 | g0137 | AMR | CLM | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| HG01433 | hp1 | a0001 | c0001 | t0020 | g0236 | AMR | CLM | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0156 | AMR | CLM | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| HG01496 | hp1 | a0001 | c0001 | t0031 | g0186 | AMR | CLM | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| HG01496 | hp2 | a0001 | c0001 | t0008 | g0020 | AMR | CLM | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0264 | EUR | IBS | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| HG01516 | hp2 | a0001 | c0001 | t0003 | g0134 | EUR | IBS | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| HG01517 | hp1 | a0001 | c0001 | t0003 | g0018 | EUR | IBS | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0266 | EUR | IBS | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| HG01884 | hp1 | a0001 | c0003 | t0012 | g0144 | AFR | ACB | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| HG01884 | hp2 | a0001 | c0001 | t0005 | g0047 | AFR | ACB | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0122 | AFR | ACB | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| HG01891 | hp2 | a0001 | c0001 | t0008 | g0020 | AFR | ACB | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0022 | AMR | PEL | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0139 | AMR | PEL | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| HG01934 | hp1 | a0001 | c0001 | t0010 | g0140 | AMR | PEL | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| HG01934 | hp2 | a0001 | c0001 | t0002 | g0222 | AMR | PEL | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0138 | AMR | PEL | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| HG01952 | hp2 | a0001 | c0001 | t0002 | g0172 | AMR | PEL | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| HG01981 | hp1 | a0001 | c0001 | t0003 | g0250 | AMR | PEL | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| HG01981 | hp2 | a0001 | c0001 | t0002 | g0015 | AMR | PEL | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| HG01993 | hp1 | a0001 | c0001 | t0002 | g0167 | AMR | PEL | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| HG01993 | hp2 | a0001 | c0001 | t0003 | g0276 | AMR | PEL | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | KHV | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| HG02027 | hp2 | a0001 | c0001 | t0002 | g0209 | EAS | KHV | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| HG02040 | hp1 | a0001 | c0001 | t0005 | g0030 | EAS | KHV | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | KHV | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| HG02055 | hp1 | a0001 | c0001 | t0008 | g0257 | AFR | ACB | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| HG02055 | hp2 | a0001 | c0001 | t0015 | g0161 | AFR | ACB | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| HG02056 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | KHV | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| HG02071 | hp1 | a0001 | c0001 | t0007 | g0092 | EAS | KHV | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| HG02071 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| HG02132 | hp1 | a0001 | c0001 | t0005 | g0048 | EAS | KHV | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| HG02132 | hp2 | a0001 | c0001 | t0004 | g0116 | EAS | KHV | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | KHV | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| HG02135 | hp2 | a0001 | c0001 | t0005 | g0107 | EAS | KHV | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| HG02145 | hp1 | a0001 | c0002 | t0012 | g0052 | AFR | ACB | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0071 | AFR | ACB | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| HG02148 | hp1 | a0001 | c0001 | t0002 | g0015 | AMR | PEL | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| HG02148 | hp2 | a0001 | c0001 | t0007 | g0251 | AMR | PEL | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0267 | EAS | CDX | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| HG02155 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | CDX | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| HG02257 | hp1 | a0001 | c0001 | t0007 | g0130 | AFR | ACB | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| HG02257 | hp2 | a0001 | c0002 | t0012 | g0143 | AFR | ACB | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0162 | AFR | ACB | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| HG02258 | hp2 | a0001 | c0001 | t0004 | g0150 | AFR | ACB | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| HG02280 | hp1 | a0001 | c0001 | t0015 | g0011 | AFR | ACB | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| HG02280 | hp2 | a0001 | c0001 | t0004 | g0149 | AFR | ACB | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| HG02293 | hp1 | a0001 | c0001 | t0022 | g0163 | AMR | PEL | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0022 | AMR | PEL | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0067 | AFR | ACB | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0102 | AFR | ACB | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0070 | AFR | GWD | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| HG02572 | hp2 | a0001 | c0001 | t0004 | g0079 | AFR | GWD | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| HG02602 | hp1 | a0001 | c0001 | t0003 | g0241 | SAS | PJL | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| HG02602 | hp2 | a0001 | c0001 | t0004 | g0118 | SAS | PJL | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| HG02615 | hp1 | a0001 | c0001 | t0004 | g0151 | AFR | GWD | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| HG02615 | hp2 | a0001 | c0001 | t0004 | g0115 | AFR | GWD | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | GWD | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| HG02630 | hp1 | a0001 | c0001 | t0009 | g0034 | AFR | GWD | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| HG02630 | hp2 | a0001 | c0001 | t0004 | g0105 | AFR | GWD | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| HG02647 | hp1 | a0001 | c0001 | t0009 | g0006 | AFR | GWD | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| HG02647 | hp2 | a0001 | c0001 | t0011 | g0073 | AFR | GWD | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| HG02717 | hp1 | a0001 | c0001 | t0004 | g0201 | AFR | GWD | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| HG02717 | hp2 | a0001 | c0002 | t0012 | g0069 | AFR | GWD | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0104 | AFR | GWD | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| HG02723 | hp2 | a0001 | c0001 | t0019 | g0059 | AFR | GWD | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| HG02735 | hp1 | a0001 | c0001 | t0013 | g0041 | SAS | PJL | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| HG02809 | hp1 | a0001 | c0001 | t0016 | g0246 | AFR | GWD | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0101 | AFR | GWD | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| HG02886 | hp1 | a0001 | c0001 | t0015 | g0011 | AFR | GWD | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| HG02886 | hp2 | a0001 | c0001 | t0004 | g0202 | AFR | GWD | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| HG02895 | hp1 | a0001 | c0001 | t0018 | g0153 | AFR | GWD | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| HG02895 | hp2 | a0001 | c0001 | t0004 | g0014 | AFR | GWD | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| HG02896 | hp1 | a0001 | c0001 | t0009 | g0006 | AFR | GWD | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| HG02896 | hp2 | a0001 | c0001 | t0019 | g0212 | AFR | GWD | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| HG02897 | hp1 | a0001 | c0001 | t0004 | g0014 | AFR | GWD | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| HG02897 | hp2 | a0001 | c0001 | t0009 | g0036 | AFR | GWD | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0078 | AFR | ESN | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| HG02965 | hp2 | a0001 | c0001 | t0010 | g0017 | AFR | ESN | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| HG02976 | hp1 | a0001 | c0001 | t0008 | g0031 | AFR | ESN | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| HG02976 | hp2 | a0001 | c0001 | t0010 | g0125 | AFR | ESN | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| HG03017 | hp1 | a0001 | c0001 | t0004 | g0008 | SAS | PJL | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| HG03017 | hp2 | a0001 | c0001 | t0013 | g0040 | SAS | PJL | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| HG03041 | hp1 | a0001 | c0001 | t0008 | g0155 | AFR | GWD | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0224 | AFR | GWD | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| HG03098 | hp1 | a0001 | c0001 | t0008 | g0053 | AFR | MSL | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0146 | AFR | MSL | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| HG03130 | hp1 | a0001 | c0001 | t0011 | g0005 | AFR | ESN | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| HG03130 | hp2 | a0001 | c0001 | t0005 | g0027 | AFR | ESN | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | ESN | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| HG03139 | hp2 | a0001 | c0002 | t0030 | g0075 | AFR | ESN | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| HG03195 | hp1 | a0001 | c0001 | t0004 | g0055 | AFR | ESN | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0223 | AFR | ESN | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | MSL | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| HG03209 | hp2 | a0001 | c0001 | t0011 | g0145 | AFR | MSL | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0033 | AFR | MSL | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0043 | AFR | MSL | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| HG03239 | hp1 | a0001 | c0001 | t0002 | g0199 | SAS | PJL | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0021 | SAS | PJL | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| HG03453 | hp1 | a0001 | c0001 | t0014 | g0147 | AFR | MSL | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| HG03453 | hp2 | a0001 | c0001 | t0004 | g0080 | AFR | MSL | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| HG03486 | hp1 | a0001 | c0001 | t0009 | g0023 | AFR | MSL | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| HG03486 | hp2 | a0001 | c0001 | t0026 | g0037 | AFR | MSL | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| HG03490 | hp1 | a0001 | c0001 | t0003 | g0237 | SAS | PJL | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| HG03490 | hp2 | a0001 | c0001 | t0013 | g0042 | SAS | PJL | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| HG03491 | hp1 | a0001 | c0001 | t0003 | g0231 | SAS | PJL | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| HG03492 | hp1 | a0001 | c0001 | t0003 | g0239 | SAS | PJL | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| HG03516 | hp1 | a0001 | c0001 | t0005 | g0029 | AFR | ESN | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0066 | AFR | ESN | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| HG03540 | hp1 | a0001 | c0001 | t0009 | g0035 | AFR | GWD | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| HG03540 | hp2 | a0001 | c0001 | t0018 | g0077 | AFR | GWD | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0204 | AFR | MSL | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0225 | AFR | MSL | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| HG03654 | hp1 | a0001 | c0001 | t0006 | g0215 | SAS | PJL | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| HG03654 | hp2 | a0001 | c0001 | t0004 | g0221 | SAS | PJL | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| HG03669 | hp1 | a0001 | c0001 | t0032 | g0277 | SAS | PJL | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0269 | SAS | PJL | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| HG03688 | hp1 | a0001 | c0001 | t0013 | g0068 | SAS | STU | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| HG03688 | hp2 | a0001 | c0001 | t0002 | g0181 | SAS | STU | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0265 | SAS | PJL | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| HG03704 | hp2 | a0001 | c0001 | t0004 | g0008 | SAS | PJL | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| HG03831 | hp1 | a0001 | c0001 | t0004 | g0117 | SAS | BEB | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0270 | SAS | BEB | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| HG03834 | hp1 | a0001 | c0001 | t0023 | g0208 | SAS | BEB | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| HG03834 | hp2 | a0001 | c0001 | t0004 | g0106 | SAS | BEB | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| HG03927 | hp1 | a0001 | c0001 | t0025 | g0273 | SAS | BEB | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| HG03927 | hp2 | a0001 | c0001 | t0002 | g0176 | SAS | BEB | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| HG03942 | hp1 | a0001 | c0001 | t0006 | g0219 | SAS | BEB | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| HG03942 | hp2 | a0001 | c0001 | t0029 | g0113 | SAS | BEB | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| HG04199 | hp1 | a0001 | c0001 | t0004 | g0112 | SAS | STU | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0272 | SAS | STU | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| HG04204 | hp1 | a0001 | c0001 | t0017 | g0214 | SAS | STU | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| HG04204 | hp2 | a0001 | c0001 | t0003 | g0242 | SAS | STU | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0160 | SAS | STU | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| HG04228 | hp2 | a0001 | c0001 | t0028 | g0278 | SAS | STU | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| NA18522 | hp1 | a0001 | c0001 | t0008 | g0032 | AFR | YRI | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| NA18522 | hp2 | a0001 | c0001 | t0010 | g0017 | AFR | YRI | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| NA18747 | hp1 | a0001 | c0001 | t0002 | g0090 | EAS | CHB | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| NA18747 | hp2 | a0001 | c0001 | t0002 | g0171 | EAS | CHB | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0203 | AFR | YRI | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| NA18906 | hp2 | a0001 | c0001 | t0011 | g0074 | AFR | YRI | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| NA18941 | hp1 | a0001 | c0001 | t0002 | g0165 | EAS | JPT | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| NA18942 | hp1 | a0001 | c0001 | t0003 | g0248 | EAS | JPT | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| NA18944 | hp1 | a0001 | c0001 | t0004 | g0136 | EAS | JPT | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| NA18944 | hp2 | a0001 | c0001 | t0002 | g0197 | EAS | JPT | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| NA18945 | hp2 | a0001 | c0001 | t0004 | g0007 | EAS | JPT | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| NA18952 | hp1 | a0001 | c0001 | t0017 | g0216 | EAS | JPT | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| NA18956 | hp1 | a0001 | c0001 | t0007 | g0230 | EAS | JPT | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| NA18956 | hp2 | a0001 | c0001 | t0002 | g0099 | EAS | JPT | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| NA18957 | hp1 | a0001 | c0001 | t0002 | g0192 | EAS | JPT | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| NA18957 | hp2 | a0001 | c0001 | t0004 | g0007 | EAS | JPT | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| NA18960 | hp1 | a0001 | c0001 | t0002 | g0175 | EAS | JPT | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| NA18960 | hp2 | a0001 | c0001 | t0002 | g0194 | EAS | JPT | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| NA18964 | hp1 | a0001 | c0001 | t0004 | g0063 | EAS | JPT | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| NA18964 | hp2 | a0001 | c0001 | t0005 | g0025 | EAS | JPT | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| NA18965 | hp1 | a0001 | c0001 | t0002 | g0082 | EAS | JPT | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| NA18965 | hp2 | a0001 | c0001 | t0004 | g0111 | EAS | JPT | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| NA18967 | hp1 | a0001 | c0001 | t0003 | g0249 | EAS | JPT | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| NA18967 | hp2 | a0001 | c0001 | t0002 | g0168 | EAS | JPT | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| NA18970 | hp2 | a0001 | c0001 | t0004 | g0062 | EAS | JPT | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| NA18972 | hp1 | a0001 | c0001 | t0007 | g0228 | EAS | JPT | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| NA18972 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| NA18973 | hp1 | a0001 | c0001 | t0006 | g0121 | EAS | JPT | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| NA18974 | hp1 | a0001 | c0001 | t0006 | g0220 | EAS | JPT | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| NA18974 | hp2 | a0001 | c0001 | t0002 | g0206 | EAS | JPT | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| NA18975 | hp1 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| NA18975 | hp2 | a0001 | c0001 | t0006 | g0119 | EAS | JPT | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| NA18979 | hp1 | a0001 | c0001 | t0002 | g0261 | EAS | JPT | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| NA18979 | hp2 | a0001 | c0001 | t0005 | g0039 | EAS | JPT | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| NA18982 | hp2 | a0001 | c0001 | t0002 | g0198 | EAS | JPT | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| NA18984 | hp1 | a0001 | c0001 | t0002 | g0271 | EAS | JPT | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| NA18984 | hp2 | a0001 | c0001 | t0003 | g0133 | EAS | JPT | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| NA18985 | hp1 | a0001 | c0001 | t0004 | g0279 | EAS | JPT | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| NA18985 | hp2 | a0001 | c0001 | t0002 | g0098 | EAS | JPT | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| NA18988 | hp1 | a0001 | c0001 | t0005 | g0024 | EAS | JPT | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| NA18988 | hp2 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| NA18990 | hp1 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| NA18990 | hp2 | a0001 | c0001 | t0003 | g0254 | EAS | JPT | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| NA18991 | hp1 | a0001 | c0001 | t0003 | g0247 | EAS | JPT | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| NA18991 | hp2 | a0001 | c0001 | t0002 | g0084 | EAS | JPT | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| NA18994 | hp1 | a0001 | c0001 | t0002 | g0262 | EAS | JPT | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| NA18994 | hp2 | a0001 | c0001 | t0003 | g0240 | EAS | JPT | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| NA18995 | hp1 | a0001 | c0001 | t0007 | g0227 | EAS | JPT | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| NA18998 | hp1 | a0001 | c0001 | t0007 | g0004 | EAS | JPT | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| NA18998 | hp2 | a0001 | c0001 | t0002 | g0083 | EAS | JPT | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| NA19001 | hp1 | a0001 | c0001 | t0003 | g0123 | EAS | JPT | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| NA19001 | hp2 | a0001 | c0001 | t0002 | g0081 | EAS | JPT | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| NA19002 | hp1 | a0001 | c0001 | t0002 | g0097 | EAS | JPT | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| NA19002 | hp2 | a0001 | c0001 | t0002 | g0091 | EAS | JPT | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| NA19007 | hp2 | a0001 | c0001 | t0006 | g0120 | EAS | JPT | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| NA19010 | hp1 | a0001 | c0001 | t0007 | g0229 | EAS | JPT | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| NA19010 | hp2 | a0001 | c0001 | t0005 | g0051 | EAS | JPT | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| NA19011 | hp1 | a0001 | c0001 | t0002 | g0193 | EAS | JPT | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| NA19011 | hp2 | a0001 | c0001 | t0004 | g0061 | EAS | JPT | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0200 | AFR | LWK | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| NA19030 | hp2 | a0001 | c0001 | t0007 | g0280 | AFR | LWK | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0060 | AFR | LWK | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| NA19043 | hp2 | a0001 | c0001 | t0027 | g0142 | AFR | LWK | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| NA19057 | hp1 | a0001 | c0001 | t0003 | g0127 | EAS | JPT | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| NA19057 | hp2 | a0001 | c0001 | t0002 | g0166 | EAS | JPT | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| NA19063 | hp2 | a0001 | c0001 | t0003 | g0124 | EAS | JPT | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| NA19065 | hp1 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| NA19065 | hp2 | a0001 | c0001 | t0006 | g0126 | EAS | JPT | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| NA19068 | hp1 | a0001 | c0001 | t0003 | g0233 | EAS | JPT | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| NA19068 | hp2 | a0001 | c0001 | t0004 | g0064 | EAS | JPT | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| NA19079 | hp2 | a0001 | c0001 | t0002 | g0100 | EAS | JPT | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| NA19085 | hp1 | a0001 | c0001 | t0004 | g0253 | EAS | JPT | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| NA19085 | hp2 | a0002 | c0004 | t0002 | g0170 | EAS | JPT | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| NA19090 | hp1 | a0001 | c0001 | t0005 | g0045 | EAS | JPT | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| NA19090 | hp2 | a0001 | c0001 | t0002 | g0263 | EAS | JPT | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| NA19091 | hp1 | a0001 | c0001 | t0002 | g0177 | EAS | JPT | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| NA19091 | hp2 | a0001 | c0001 | t0003 | g0232 | EAS | JPT | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0021 | EUR | TSI | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| NA20752 | hp2 | a0001 | c0001 | t0006 | g0217 | EUR | TSI | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| NA20805 | hp1 | a0001 | c0001 | t0002 | g0180 | EUR | TSI | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0260 | EUR | TSI | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0054 | AFR | ACB | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| HG02109 | hp2 | a0001 | c0003 | t0012 | g0072 | AFR | ACB | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0205 | AFR | ACB | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| HG02486 | hp2 | a0001 | c0001 | t0005 | g0050 | AFR | ACB | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| HG02559 | hp1 | a0001 | c0001 | t0011 | g0005 | AFR | ACB | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0243 | AFR | ACB | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| HG03471 | hp1 | a0001 | c0001 | t0014 | g0148 | AFR | MSL | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| HG03471 | hp2 | a0001 | c0001 | t0005 | g0049 | AFR | MSL | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0103 | AFR | USA | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| HG06807 | hp2 | a0001 | c0001 | t0005 | g0044 | AFR | USA | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| NA20300 | hp1 | a0001 | c0001 | t0014 | g0076 | AFR | USA | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| NA20300 | hp2 | a0001 | c0001 | t0003 | g0244 | AFR | USA | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0038 | AFR | LWK | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| NA21309 | hp2 | a0001 | c0001 | t0005 | g0028 | AFR | LWK | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0024 | g0226 | REF | REF | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0002 | g0089 | REF | REF | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:145482037 | C | T | 1 | a0001 | 2 | HG01070.hp2 HG01433.hp1 |
splice_region_variant | LOW | c.-178C>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/7 | chr4 | 145482037 | |||||||
| chr4:145514438 | G | A | 1 | a0001 | 7 | HG01261.hp1 HG02630.hp1 HG02647.hp1 others(4): Show |
splice_region_variant | LOW | c.-176G>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/7 | chr4 | 145514438 | |||||||
| chr4:145553894 | A | G | 1 | a0002 | 1 | NA19085.hp2 | missense_variant | MODERATE | c.1108A>G | p.Thr370Ala | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 6/7 | 1470/3002 | 1108/1398 | 370/465 | chr4 | 145553894 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:145514998 | A | C | 2 | a0001c0002 a0001c0003 |
6 | HG01884.hp1 HG02109.hp2 HG02145.hp1 others(3): Show |
synonymous_variant | LOW | c.385A>C | p.Arg129Arg | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/7 | 747/3002 | 385/1398 | 129/465 | chr4 | 145514998 | |||
| chr4:145542670 | T | C | 1 | a0001c0003 | 2 | HG01884.hp1 HG02109.hp2 |
synonymous_variant | LOW | c.747T>C | p.Pro249Pro | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 4/7 | 1109/3002 | 747/1398 | 249/465 | chr4 | 145542670 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:145481985 | C | G | 1 | a0001c0001t0032 | 1 | HG03669.hp1 | 5_prime_UTR_variant | MODIFIER | c.-230C>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/7 | 32629 | chr4 | 145481985 | ||||||
| chr4:145481988 | C | T | 1 | a0001c0001t0031 | 1 | HG01496.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-227C>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/7 | chr4 | 145481988 | |||||||
| chr4:145482013 | A | G | 28 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(25): Show |
239 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(236): Show |
5_prime_UTR_variant | MODIFIER | c.-202A>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/7 | 32601 | chr4 | 145482013 | ||||||
| chr4:145514452 | A | G | 3 | a0001c0002t0012 a0001c0002t0030 a0001c0003t0012 |
6 | HG01884.hp1 HG02109.hp2 HG02145.hp1 others(3): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-162A>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/7 | chr4 | 145514452 | |||||||
| chr4:145558079 | C | CA | 10 | a0001c0001t0003 a0001c0001t0010 a0001c0001t0013 others(7): Show |
60 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(57): Show |
3_prime_UTR_variant | MODIFIER | c.*160dupA | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 7/7 | 161 | INFO_REALIGN_3_PRIME | chr4 | 145558079 | |||||
| chr4:145558082 | A | AC | 4 | a0001c0001t0015 a0001c0001t0027 a0001c0001t0028 others(1): Show |
6 | HG02055.hp2 HG02280.hp1 HG02886.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*148_*149insC | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 7/7 | 149 | chr4 | 145558082 | ||||||
| chr4:145558083 | A | C | 6 | a0001c0001t0004 a0001c0001t0005 a0001c0001t0009 others(3): Show |
64 | HG00423.hp2 HG00438.hp1 HG00621.hp1 others(61): Show |
3_prime_UTR_variant | MODIFIER | c.*149A>C | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 7/7 | 149 | chr4 | 145558083 | ||||||
| chr4:145558094 | AC | A | 3 | a0001c0001t0001 a0001c0001t0007 a0001c0001t0018 |
12 | HG02145.hp2 HG02451.hp1 HG02895.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*161delC | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 7/7 | 161 | chr4 | 145558094 | ||||||
| chr4:145558095 | C | A | 14 | a0001c0001t0003 a0001c0001t0006 a0001c0001t0007 others(11): Show |
79 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(76): Show |
3_prime_UTR_variant | MODIFIER | c.*161C>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 7/7 | 161 | chr4 | 145558095 | ||||||
| chr4:145558136 | T | C | 1 | a0001c0001t0026 | 1 | HG03486.hp2 | 3_prime_UTR_variant | MODIFIER | c.*202T>C | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 7/7 | 202 | chr4 | 145558136 | ||||||
| chr4:145558245 | A | G | 3 | a0001c0001t0006 a0001c0001t0017 a0001c0001t0025 |
13 | HG00738.hp2 HG01081.hp2 HG03654.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*311A>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 7/7 | 311 | chr4 | 145558245 | ||||||
| chr4:145558326 | T | A | 1 | a0001c0001t0018 | 2 | HG02895.hp1 HG03540.hp2 |
3_prime_UTR_variant | MODIFIER | c.*392T>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 7/7 | 392 | chr4 | 145558326 | ||||||
| chr4:145558335 | G | A | 1 | a0001c0001t0022 | 1 | HG02293.hp1 | 3_prime_UTR_variant | MODIFIER | c.*401G>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 7/7 | 401 | chr4 | 145558335 | ||||||
| chr4:145558515 | A | G | 1 | a0001c0001t0019 | 2 | HG02723.hp2 HG02896.hp2 |
3_prime_UTR_variant | MODIFIER | c.*581A>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 7/7 | 581 | chr4 | 145558515 | ||||||
| chr4:145558549 | T | G | 1 | a0001c0001t0015 | 3 | HG02055.hp2 HG02280.hp1 HG02886.hp1 |
3_prime_UTR_variant | MODIFIER | c.*615T>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 7/7 | 615 | chr4 | 145558549 | ||||||
| chr4:145558681 | G | T | 1 | a0001c0001t0011 | 5 | HG02559.hp1 HG02647.hp2 HG03130.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*747G>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 7/7 | 747 | chr4 | 145558681 | ||||||
| chr4:145558684 | AC | A | 5 | a0001c0001t0004 a0001c0001t0013 a0001c0001t0023 others(2): Show |
41 | HG00423.hp2 HG00621.hp1 HG01175.hp1 others(38): Show |
3_prime_UTR_variant | MODIFIER | c.*752delC | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 7/7 | 752 | INFO_REALIGN_3_PRIME | chr4 | 145558684 | |||||
| chr4:145558697 | T | C | 1 | a0001c0001t0015 | 3 | HG02055.hp2 HG02280.hp1 HG02886.hp1 |
3_prime_UTR_variant | MODIFIER | c.*763T>C | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 7/7 | 763 | chr4 | 145558697 | ||||||
| chr4:145558740 | C | CTT | 25 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0005 others(22): Show |
159 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(156): Show |
3_prime_UTR_variant | MODIFIER | c.*806_*807insTT | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 7/7 | 807 | chr4 | 145558740 | ||||||
| chr4:145558740 | C | T | 1 | a0001c0001t0016 | 2 | HG01169.hp1 HG02809.hp1 |
3_prime_UTR_variant | MODIFIER | c.*806C>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 7/7 | 806 | chr4 | 145558740 | ||||||
| chr4:145558787 | T | C | 1 | a0001c0001t0025 | 1 | HG03927.hp1 | 3_prime_UTR_variant | MODIFIER | c.*853T>C | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 7/7 | 853 | chr4 | 145558787 | ||||||
| chr4:145558959 | T | C | 3 | a0001c0001t0008 a0001c0001t0014 a0001c0001t0018 |
13 | HG01192.hp2 HG01496.hp2 HG01891.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*1025T>C | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 7/7 | 1025 | chr4 | 145558959 | ||||||
| chr4:145559078 | A | T | 1 | a0001c0001t0028 | 1 | HG04228.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1144A>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 7/7 | 1144 | chr4 | 145559078 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:145482223 | A | AC | 127 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0146 others(124): Show |
145 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(142): Show |
intron_variant | MODIFIER | c.-177+197dupC | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr4 | 145482223 | ||||||
| chr4:145482223 | A | ACC | 26 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0258 others(23): Show |
29 | HG00140.hp1 HG00673.hp1 HG00735.hp1 others(26): Show |
intron_variant | MODIFIER | c.-177+196_-177+197d others(4): Show |
SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr4 | 145482223 | ||||||
| chr4:145482223 | AC | A | 32 | a0001c0001t0001g0009 a0001c0001t0001g0043 a0001c0001t0001g0054 others(29): Show |
37 | HG00438.hp1 HG01167.hp1 HG01884.hp2 others(34): Show |
intron_variant | MODIFIER | c.-177+197delC | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr4 | 145482223 | ||||||
| chr4:145482223 | ACC | A | 20 | a0001c0001t0001g0033 a0001c0001t0001g0038 a0001c0001t0005g0024 others(17): Show |
20 | HG01243.hp2 HG02040.hp1 HG02630.hp1 others(17): Show |
intron_variant | MODIFIER | c.-177+196_-177+197d others(4): Show |
SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr4 | 145482223 | ||||||
| chr4:145482227 | C | G | 1 | a0001c0001t0007g0280 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-177+189C>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145482227 | |||||||
| chr4:145482231 | C | G | 1 | a0001c0001t0004g0279 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.-177+193C>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145482231 | |||||||
| chr4:145482377 | G | T | 6 | a0001c0001t0001g0066 a0001c0001t0001g0067 a0001c0001t0013g0040 others(3): Show |
6 | HG02451.hp1 HG02735.hp1 HG03017.hp2 others(3): Show |
intron_variant | MODIFIER | c.-177+339G>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145482377 | |||||||
| chr4:145482389 | G | T | 1 | a0001c0001t0013g0042 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.-177+351G>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145482389 | |||||||
| chr4:145482397 | C | T | 1 | a0001c0001t0028g0278 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.-177+359C>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145482397 | |||||||
| chr4:145482420 | G | A | 2 | a0001c0001t0001g0066 a0001c0001t0001g0067 |
2 | HG02451.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.-177+382G>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145482420 | |||||||
| chr4:145482495 | C | T | 4 | a0001c0001t0001g0138 a0001c0001t0001g0139 a0001c0001t0001g0141 others(1): Show |
4 | HG01081.hp1 HG01928.hp2 HG01934.hp1 others(1): Show |
intron_variant | MODIFIER | c.-177+457C>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145482495 | |||||||
| chr4:145482496 | C | T | 54 | a0001c0001t0001g0243 a0001c0001t0003g0004 a0001c0001t0003g0016 others(51): Show |
59 | HG00099.hp1 HG00408.hp1 HG00597.hp2 others(56): Show |
intron_variant | MODIFIER | c.-177+458C>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145482496 | |||||||
| chr4:145482618 | C | T | 1 | a0001c0001t0002g0015 | 2 | HG01981.hp2 HG02148.hp1 |
intron_variant | MODIFIER | c.-177+580C>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145482618 | |||||||
| chr4:145482693 | C | G | 1 | a0001c0001t0003g0255 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.-177+655C>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145482693 | |||||||
| chr4:145482787 | T | C | 1 | a0001c0001t0027g0142 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-177+749T>C | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145482787 | |||||||
| chr4:145482791 | G | A | 2 | a0001c0002t0012g0069 a0001c0002t0012g0143 |
2 | HG02257.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.-177+753G>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145482791 | |||||||
| chr4:145482857 | C | T | 1 | a0001c0001t0002g0015 | 2 | HG01981.hp2 HG02148.hp1 |
intron_variant | MODIFIER | c.-177+819C>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145482857 | |||||||
| chr4:145483109 | G | C | 1 | a0001c0001t0001g0070 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-177+1071G>C | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145483109 | |||||||
| chr4:145483116 | C | T | 1 | a0001c0001t0003g0254 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.-177+1078C>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145483116 | |||||||
| chr4:145483206 | C | T | 1 | a0001c0001t0005g0039 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.-177+1168C>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145483206 | |||||||
| chr4:145483290 | T | G | 66 | a0001c0001t0001g0003 a0001c0001t0001g0033 a0001c0001t0001g0043 others(63): Show |
72 | HG00438.hp1 HG01192.hp2 HG01243.hp1 others(69): Show |
intron_variant | MODIFIER | c.-177+1252T>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145483290 | |||||||
| chr4:145483390 | C | G | 7 | a0001c0001t0001g0054 a0001c0001t0001g0078 a0001c0001t0001g0162 others(4): Show |
8 | HG02055.hp2 HG02109.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.-177+1352C>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145483390 | |||||||
| chr4:145483500 | A | G | 5 | a0001c0001t0001g0122 a0001c0001t0001g0223 a0001c0001t0001g0224 others(2): Show |
6 | HG01891.hp1 HG02895.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.-177+1462A>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145483500 | |||||||
| chr4:145483704 | G | A | 60 | a0001c0001t0001g0033 a0001c0001t0001g0043 a0001c0001t0001g0054 others(57): Show |
64 | HG00438.hp1 HG01192.hp2 HG01243.hp1 others(61): Show |
intron_variant | MODIFIER | c.-177+1666G>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145483704 | |||||||
| chr4:145483991 | C | T | 1 | a0001c0001t0003g0137 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.-177+1953C>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145483991 | |||||||
| chr4:145484001 | T | G | 35 | a0001c0001t0001g0043 a0001c0001t0001g0071 a0001c0001t0001g0146 others(32): Show |
36 | HG00438.hp1 HG01243.hp1 HG01243.hp2 others(33): Show |
intron_variant | MODIFIER | c.-177+1963T>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145484001 | |||||||
| chr4:145484017 | AGTT | A | 2 | a0001c0001t0001g0021 a0001c0001t0001g0258 |
3 | HG00735.hp1 HG03239.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.-177+1982_-177+198 others(7): Show |
SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr4 | 145484017 | ||||||
| chr4:145484559 | G | A | 1 | a0001c0001t0016g0275 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.-177+2521G>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145484559 | |||||||
| chr4:145484641 | A | G | 1 | a0001c0001t0027g0142 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-177+2603A>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145484641 | |||||||
| chr4:145484660 | A | C | 11 | a0001c0001t0001g0054 a0001c0001t0001g0078 a0001c0001t0001g0157 others(8): Show |
12 | HG02055.hp2 HG02109.hp1 HG02135.hp1 others(9): Show |
intron_variant | MODIFIER | c.-177+2622A>C | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145484660 | |||||||
| chr4:145484869 | T | A | 11 | a0001c0001t0001g0054 a0001c0001t0001g0078 a0001c0001t0001g0157 others(8): Show |
12 | HG02055.hp2 HG02109.hp1 HG02135.hp1 others(9): Show |
intron_variant | MODIFIER | c.-177+2831T>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145484869 | |||||||
| chr4:145484998 | C | T | 1 | a0001c0001t0002g0274 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.-177+2960C>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145484998 | |||||||
| chr4:145485040 | C | T | 1 | a0001c0001t0002g0222 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.-177+3002C>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145485040 | |||||||
| chr4:145485278 | G | A | 4 | a0001c0001t0001g0043 a0001c0001t0001g0071 a0001c0003t0012g0072 others(1): Show |
4 | HG01884.hp1 HG02109.hp2 HG02145.hp2 others(1): Show |
intron_variant | MODIFIER | c.-177+3240G>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145485278 | |||||||
| chr4:145485327 | C | T | 5 | a0001c0001t0008g0020 a0001c0001t0008g0053 a0001c0001t0008g0155 others(2): Show |
6 | HG01192.hp2 HG01496.hp2 HG01891.hp2 others(3): Show |
intron_variant | MODIFIER | c.-177+3289C>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145485327 | |||||||
| chr4:145485419 | G | A | 1 | a0001c0002t0012g0143 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-177+3381G>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145485419 | |||||||
| chr4:145485536 | T | G | 64 | a0001c0001t0001g0033 a0001c0001t0001g0043 a0001c0001t0001g0054 others(61): Show |
68 | HG00438.hp1 HG01192.hp2 HG01243.hp1 others(65): Show |
intron_variant | MODIFIER | c.-177+3498T>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145485536 | |||||||
| chr4:145485741 | C | G | 16 | a0001c0001t0001g0122 a0001c0001t0001g0223 a0001c0001t0001g0224 others(13): Show |
17 | HG00738.hp2 HG01081.hp2 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.-177+3703C>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145485741 | |||||||
| chr4:145485793 | C | CT | 16 | a0001c0001t0005g0024 a0001c0001t0005g0025 a0001c0001t0005g0026 others(13): Show |
16 | HG00438.hp1 HG01243.hp2 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.-177+3761dupT | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr4 | 145485793 | ||||||
| chr4:145486246 | G | A | 4 | a0001c0001t0001g0043 a0001c0001t0001g0071 a0001c0003t0012g0072 others(1): Show |
4 | HG01884.hp1 HG02109.hp2 HG02145.hp2 others(1): Show |
intron_variant | MODIFIER | c.-177+4208G>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145486246 | |||||||
| chr4:145486372 | A | G | 64 | a0001c0001t0001g0033 a0001c0001t0001g0043 a0001c0001t0001g0054 others(61): Show |
68 | HG00438.hp1 HG01192.hp2 HG01243.hp1 others(65): Show |
intron_variant | MODIFIER | c.-177+4334A>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145486372 | |||||||
| chr4:145486528 | C | CT | 64 | a0001c0001t0001g0033 a0001c0001t0001g0043 a0001c0001t0001g0054 others(61): Show |
68 | HG00438.hp1 HG01192.hp2 HG01243.hp1 others(65): Show |
intron_variant | MODIFIER | c.-177+4490_-177+449 others(5): Show |
SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145486528 | |||||||
| chr4:145486720 | C | T | 64 | a0001c0001t0001g0033 a0001c0001t0001g0043 a0001c0001t0001g0054 others(61): Show |
68 | HG00438.hp1 HG01192.hp2 HG01243.hp1 others(65): Show |
intron_variant | MODIFIER | c.-177+4682C>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145486720 | |||||||
| chr4:145486912 | G | A | 2 | a0001c0001t0008g0031 a0001c0001t0008g0032 |
2 | HG02976.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-177+4874G>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145486912 | |||||||
| chr4:145486978 | T | G | 4 | a0001c0001t0011g0005 a0001c0001t0011g0073 a0001c0001t0011g0074 others(1): Show |
5 | HG02559.hp1 HG02647.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.-177+4940T>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145486978 | |||||||
| chr4:145487140 | G | A | 1 | a0001c0001t0001g0259 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-177+5102G>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145487140 | |||||||
| chr4:145487183 | A | G | 4 | a0001c0001t0001g0043 a0001c0001t0001g0071 a0001c0003t0012g0072 others(1): Show |
4 | HG01884.hp1 HG02109.hp2 HG02145.hp2 others(1): Show |
intron_variant | MODIFIER | c.-177+5145A>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145487183 | |||||||
| chr4:145487294 | A | G | 35 | a0001c0001t0001g0033 a0001c0001t0001g0146 a0001c0001t0004g0149 others(32): Show |
36 | HG00438.hp1 HG01243.hp1 HG01243.hp2 others(33): Show |
intron_variant | MODIFIER | c.-177+5256A>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145487294 | |||||||
| chr4:145487358 | G | T | 2 | a0001c0001t0008g0031 a0001c0001t0008g0032 |
2 | HG02976.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-177+5320G>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145487358 | |||||||
| chr4:145487372 | T | C | 7 | a0001c0001t0001g0033 a0001c0001t0009g0006 a0001c0001t0009g0034 others(4): Show |
8 | HG01261.hp1 HG02630.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.-177+5334T>C | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145487372 | |||||||
| chr4:145487786 | G | A | 4 | a0001c0001t0005g0024 a0001c0001t0005g0025 a0001c0001t0005g0045 others(1): Show |
4 | HG00438.hp1 NA18964.hp2 NA18988.hp1 others(1): Show |
intron_variant | MODIFIER | c.-177+5748G>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145487786 | |||||||
| chr4:145487805 | C | T | 4 | a0001c0001t0001g0043 a0001c0001t0001g0071 a0001c0003t0012g0072 others(1): Show |
4 | HG01884.hp1 HG02109.hp2 HG02145.hp2 others(1): Show |
intron_variant | MODIFIER | c.-177+5767C>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145487805 | |||||||
| chr4:145487828 | G | A | 1 | a0001c0001t0003g0254 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.-177+5790G>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145487828 | |||||||
| chr4:145487881 | AG | A | 60 | a0001c0001t0001g0033 a0001c0001t0001g0043 a0001c0001t0001g0054 others(57): Show |
64 | HG00438.hp1 HG01192.hp2 HG01243.hp1 others(61): Show |
intron_variant | MODIFIER | c.-177+5844delG | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145487881 | |||||||
| chr4:145488079 | T | C | 60 | a0001c0001t0001g0033 a0001c0001t0001g0043 a0001c0001t0001g0054 others(57): Show |
64 | HG00438.hp1 HG01192.hp2 HG01243.hp1 others(61): Show |
intron_variant | MODIFIER | c.-177+6041T>C | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145488079 | |||||||
| chr4:145488120 | CT | C | 14 | a0001c0001t0004g0055 a0001c0001t0004g0079 a0001c0001t0004g0080 others(11): Show |
14 | HG00738.hp2 HG01081.hp2 HG02572.hp2 others(11): Show |
intron_variant | MODIFIER | c.-177+6094delT | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr4 | 145488120 | ||||||
| chr4:145488313 | C | G | 9 | a0001c0001t0001g0043 a0001c0001t0001g0071 a0001c0001t0011g0005 others(6): Show |
10 | HG01884.hp1 HG02109.hp2 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.-177+6275C>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145488313 | |||||||
| chr4:145488400 | A | T | 51 | a0001c0001t0001g0033 a0001c0001t0001g0054 a0001c0001t0001g0078 others(48): Show |
54 | HG00438.hp1 HG01192.hp2 HG01243.hp1 others(51): Show |
intron_variant | MODIFIER | c.-177+6362A>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145488400 | |||||||
| chr4:145488476 | T | TTG | 69 | a0001c0001t0001g0038 a0001c0001t0001g0066 a0001c0001t0001g0067 others(66): Show |
73 | HG00099.hp1 HG00423.hp2 HG00621.hp1 others(70): Show |
intron_variant | MODIFIER | c.-177+6465_-177+646 others(6): Show |
SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr4 | 145488476 | ||||||
| chr4:145488476 | T | TTGTG | 23 | a0001c0001t0001g0009 a0001c0001t0001g0122 a0001c0001t0001g0223 others(20): Show |
25 | HG01081.hp2 HG01167.hp1 HG01175.hp2 others(22): Show |
intron_variant | MODIFIER | c.-177+6463_-177+646 others(8): Show |
SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr4 | 145488476 | ||||||
| chr4:145488476 | TTGTGTGT others(3): Show |
T | 1 | a0001c0002t0012g0052 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-177+6457_-177+646 others(14): Show |
SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr4 | 145488476 | ||||||
| chr4:145488476 | TTGTGTGT others(5): Show |
T | 59 | a0001c0001t0001g0033 a0001c0001t0001g0043 a0001c0001t0001g0054 others(56): Show |
63 | HG00438.hp1 HG01192.hp2 HG01243.hp1 others(60): Show |
intron_variant | MODIFIER | c.-177+6455_-177+646 others(16): Show |
SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr4 | 145488476 | ||||||
| chr4:145488556 | CT | C | 60 | a0001c0001t0001g0033 a0001c0001t0001g0043 a0001c0001t0001g0054 others(57): Show |
64 | HG00438.hp1 HG01192.hp2 HG01243.hp1 others(61): Show |
intron_variant | MODIFIER | c.-177+6526delT | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr4 | 145488556 | ||||||
| chr4:145488629 | G | A | 9 | a0001c0001t0001g0043 a0001c0001t0001g0071 a0001c0001t0011g0005 others(6): Show |
10 | HG01884.hp1 HG02109.hp2 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.-177+6591G>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145488629 | |||||||
| chr4:145488697 | G | A | 7 | a0001c0001t0001g0054 a0001c0001t0001g0078 a0001c0001t0001g0162 others(4): Show |
8 | HG02055.hp2 HG02109.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.-177+6659G>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145488697 | |||||||
| chr4:145488812 | T | C | 60 | a0001c0001t0001g0033 a0001c0001t0001g0043 a0001c0001t0001g0054 others(57): Show |
64 | HG00438.hp1 HG01192.hp2 HG01243.hp1 others(61): Show |
intron_variant | MODIFIER | c.-177+6774T>C | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145488812 | |||||||
| chr4:145488830 | C | T | 17 | a0001c0001t0003g0134 a0001c0001t0003g0250 a0001c0001t0005g0024 others(14): Show |
17 | HG00438.hp1 HG01243.hp2 HG01516.hp2 others(14): Show |
intron_variant | MODIFIER | c.-177+6792C>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145488830 | |||||||
| chr4:145489227 | T | C | 1 | a0001c0001t0020g0128 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.-177+7189T>C | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145489227 | |||||||
| chr4:145489295 | G | T | 1 | a0001c0001t0003g0234 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.-177+7257G>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145489295 | |||||||
| chr4:145489364 | G | C | 1 | a0001c0001t0004g0106 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.-177+7326G>C | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145489364 | |||||||
| chr4:145489393 | G | A | 56 | a0001c0001t0001g0033 a0001c0001t0001g0043 a0001c0001t0001g0071 others(53): Show |
60 | HG00438.hp1 HG01192.hp2 HG01243.hp1 others(57): Show |
intron_variant | MODIFIER | c.-177+7355G>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145489393 | |||||||
| chr4:145489478 | TAAATA | T | 55 | a0001c0001t0001g0033 a0001c0001t0001g0043 a0001c0001t0001g0071 others(52): Show |
59 | HG00438.hp1 HG01192.hp2 HG01243.hp2 others(56): Show |
intron_variant | MODIFIER | c.-177+7449_-177+745 others(9): Show |
SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr4 | 145489478 | ||||||
| chr4:145489525 | T | C | 3 | a0001c0001t0001g0157 a0001c0001t0001g0158 a0001c0001t0003g0234 |
3 | HG00609.hp1 HG02135.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.-177+7487T>C | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145489525 | |||||||
| chr4:145489848 | G | A | 57 | a0001c0001t0001g0033 a0001c0001t0001g0043 a0001c0001t0001g0071 others(54): Show |
61 | HG00438.hp1 HG01192.hp2 HG01243.hp1 others(58): Show |
intron_variant | MODIFIER | c.-177+7810G>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145489848 | |||||||
| chr4:145490038 | A | T | 97 | a0001c0001t0001g0054 a0001c0001t0001g0066 a0001c0001t0001g0067 others(94): Show |
105 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(102): Show |
intron_variant | MODIFIER | c.-177+8000A>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145490038 | |||||||
| chr4:145490039 | A | C | 97 | a0001c0001t0001g0054 a0001c0001t0001g0066 a0001c0001t0001g0067 others(94): Show |
105 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(102): Show |
intron_variant | MODIFIER | c.-177+8001A>C | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145490039 | |||||||
| chr4:145490056 | A | C | 2 | a0001c0003t0012g0072 a0001c0003t0012g0144 |
2 | HG01884.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.-177+8018A>C | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145490056 | |||||||
| chr4:145490068 | G | A | 3 | a0001c0001t0002g0164 a0001c0001t0002g0222 a0001c0001t0022g0163 |
3 | HG01069.hp2 HG01934.hp2 HG02293.hp1 |
intron_variant | MODIFIER | c.-177+8030G>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145490068 | |||||||
| chr4:145490231 | CA | C | 42 | a0001c0001t0001g0054 a0001c0001t0001g0066 a0001c0001t0001g0067 others(39): Show |
45 | HG00423.hp2 HG00621.hp1 HG01081.hp1 others(42): Show |
intron_variant | MODIFIER | c.-177+8196delA | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr4 | 145490231 | ||||||
| chr4:145490377 | G | A | 32 | a0001c0001t0001g0033 a0001c0001t0001g0146 a0001c0001t0004g0149 others(29): Show |
33 | HG00438.hp1 HG01243.hp1 HG01243.hp2 others(30): Show |
intron_variant | MODIFIER | c.-177+8339G>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145490377 | |||||||
| chr4:145490418 | G | A | 58 | a0001c0001t0001g0033 a0001c0001t0001g0043 a0001c0001t0001g0071 others(55): Show |
62 | HG00438.hp1 HG01192.hp2 HG01243.hp1 others(59): Show |
intron_variant | MODIFIER | c.-177+8380G>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145490418 | |||||||
| chr4:145490584 | A | G | 1 | a0001c0001t0001g0141 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.-177+8546A>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145490584 | |||||||
| chr4:145490630 | C | G | 1 | a0001c0001t0001g0070 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-177+8592C>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145490630 | |||||||
| chr4:145490686 | A | T | 1 | a0001c0001t0002g0206 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.-177+8648A>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145490686 | |||||||
| chr4:145491046 | G | T | 2 | a0001c0003t0012g0072 a0001c0003t0012g0144 |
2 | HG01884.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.-177+9008G>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145491046 | |||||||
| chr4:145491130 | A | T | 2 | a0001c0001t0011g0074 a0001c0001t0011g0145 |
2 | HG03209.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.-177+9092A>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145491130 | |||||||
| chr4:145491228 | T | C | 1 | a0001c0001t0005g0026 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-177+9190T>C | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145491228 | |||||||
| chr4:145491258 | A | C | 3 | a0001c0002t0012g0052 a0001c0002t0012g0069 a0001c0002t0012g0143 |
3 | HG02145.hp1 HG02257.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.-177+9220A>C | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145491258 | |||||||
| chr4:145491531 | C | T | 1 | a0001c0001t0004g0080 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-177+9493C>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145491531 | |||||||
| chr4:145491629 | A | G | 5 | a0001c0001t0008g0020 a0001c0001t0008g0053 a0001c0001t0008g0155 others(2): Show |
6 | HG01192.hp2 HG01496.hp2 HG01891.hp2 others(3): Show |
intron_variant | MODIFIER | c.-177+9591A>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145491629 | |||||||
| chr4:145491716 | T | C | 1 | a0001c0001t0007g0280 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-177+9678T>C | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145491716 | |||||||
| chr4:145491786 | C | T | 2 | a0001c0001t0001g0043 a0001c0001t0001g0071 |
2 | HG02145.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.-177+9748C>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145491786 | |||||||
| chr4:145491810 | C | T | 1 | a0001c0002t0030g0075 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-177+9772C>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145491810 | |||||||
| chr4:145491829 | A | G | 1 | a0001c0001t0002g0271 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.-177+9791A>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145491829 | |||||||
| chr4:145491938 | A | G | 3 | a0001c0002t0012g0052 a0001c0002t0012g0069 a0001c0002t0012g0143 |
3 | HG02145.hp1 HG02257.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.-177+9900A>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145491938 | |||||||
| chr4:145491950 | G | A | 1 | a0001c0001t0004g0109 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.-177+9912G>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145491950 | |||||||
| chr4:145492012 | TA | T | 9 | a0001c0001t0001g0043 a0001c0001t0001g0071 a0001c0001t0011g0005 others(6): Show |
10 | HG01884.hp1 HG02109.hp2 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.-177+9982delA | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr4 | 145492012 | ||||||
| chr4:145492192 | C | T | 4 | a0001c0001t0003g0133 a0001c0001t0003g0247 a0001c0001t0003g0248 others(1): Show |
4 | NA18942.hp1 NA18967.hp1 NA18984.hp2 others(1): Show |
intron_variant | MODIFIER | c.-177+10154C>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145492192 | |||||||
| chr4:145492399 | C | T | 9 | a0001c0001t0001g0043 a0001c0001t0001g0071 a0001c0001t0011g0005 others(6): Show |
10 | HG01884.hp1 HG02109.hp2 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.-177+10361C>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145492399 | |||||||
| chr4:145492516 | G | T | 5 | a0001c0001t0008g0020 a0001c0001t0008g0053 a0001c0001t0008g0155 others(2): Show |
6 | HG01192.hp2 HG01496.hp2 HG01891.hp2 others(3): Show |
intron_variant | MODIFIER | c.-177+10478G>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145492516 | |||||||
| chr4:145492523 | G | A | 1 | a0001c0001t0009g0023 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-177+10485G>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145492523 | |||||||
| chr4:145492666 | C | G | 1 | a0001c0001t0027g0142 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-177+10628C>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145492666 | |||||||
| chr4:145492763 | T | A | 53 | a0001c0001t0001g0033 a0001c0001t0001g0043 a0001c0001t0001g0071 others(50): Show |
57 | HG00438.hp1 HG01192.hp2 HG01243.hp2 others(54): Show |
intron_variant | MODIFIER | c.-177+10725T>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145492763 | |||||||
| chr4:145493101 | C | G | 1 | a0001c0001t0015g0161 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-177+11063C>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145493101 | |||||||
| chr4:145493115 | A | G | 190 | a0001c0001t0001g0009 a0001c0001t0001g0013 a0001c0001t0001g0033 others(187): Show |
204 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(201): Show |
intron_variant | MODIFIER | c.-177+11077A>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145493115 | |||||||
| chr4:145493288 | G | A | 57 | a0001c0001t0001g0033 a0001c0001t0001g0043 a0001c0001t0001g0071 others(54): Show |
61 | HG00438.hp1 HG01192.hp2 HG01243.hp1 others(58): Show |
intron_variant | MODIFIER | c.-177+11250G>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145493288 | |||||||
| chr4:145493321 | T | C | 1 | a0001c0001t0013g0042 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.-177+11283T>C | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145493321 | |||||||
| chr4:145493355 | A | G | 1 | a0001c0002t0030g0075 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-177+11317A>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145493355 | |||||||
| chr4:145493448 | G | T | 1 | a0001c0002t0030g0075 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-177+11410G>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145493448 | |||||||
| chr4:145493639 | G | A | 1 | a0001c0001t0004g0105 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-177+11601G>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145493639 | |||||||
| chr4:145493648 | T | C | 2 | a0001c0001t0001g0043 a0001c0001t0001g0071 |
2 | HG02145.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.-177+11610T>C | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145493648 | |||||||
| chr4:145493736 | C | G | 2 | a0001c0001t0015g0011 a0001c0001t0015g0161 |
3 | HG02055.hp2 HG02280.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.-177+11698C>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145493736 | |||||||
| chr4:145493911 | C | G | 4 | a0001c0001t0007g0280 a0001c0001t0015g0011 a0001c0001t0015g0161 others(1): Show |
5 | HG02055.hp2 HG02280.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.-177+11873C>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145493911 | |||||||
| chr4:145493971 | A | AT | 4 | a0001c0001t0004g0008 a0001c0001t0004g0117 a0001c0001t0004g0118 others(1): Show |
5 | HG02602.hp2 HG03017.hp1 HG03654.hp2 others(2): Show |
intron_variant | MODIFIER | c.-177+11941dupT | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr4 | 145493971 | ||||||
| chr4:145494013 | G | A | 1 | a0001c0001t0004g0105 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-177+11975G>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145494013 | |||||||
| chr4:145494082 | A | G | 1 | a0001c0002t0012g0052 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-177+12044A>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145494082 | |||||||
| chr4:145494128 | GT | G | 32 | a0001c0001t0001g0033 a0001c0001t0001g0146 a0001c0001t0004g0149 others(29): Show |
33 | HG00438.hp1 HG01243.hp1 HG01243.hp2 others(30): Show |
intron_variant | MODIFIER | c.-177+12095delT | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr4 | 145494128 | ||||||
| chr4:145494199 | A | T | 57 | a0001c0001t0001g0033 a0001c0001t0001g0043 a0001c0001t0001g0071 others(54): Show |
61 | HG00438.hp1 HG01192.hp2 HG01243.hp1 others(58): Show |
intron_variant | MODIFIER | c.-177+12161A>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145494199 | |||||||
| chr4:145494252 | G | A | 1 | a0001c0002t0030g0075 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-177+12214G>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145494252 | |||||||
| chr4:145494255 | C | T | 1 | a0001c0001t0002g0199 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-177+12217C>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145494255 | |||||||
| chr4:145494281 | G | A | 4 | a0001c0001t0001g0157 a0001c0001t0001g0158 a0001c0001t0001g0159 others(1): Show |
4 | HG02135.hp1 HG04228.hp1 NA18945.hp1 others(1): Show |
intron_variant | MODIFIER | c.-177+12243G>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145494281 | |||||||
| chr4:145494486 | G | T | 12 | a0001c0001t0002g0097 a0001c0001t0002g0098 a0001c0001t0002g0099 others(9): Show |
12 | HG00423.hp1 HG00558.hp2 HG00673.hp1 others(9): Show |
intron_variant | MODIFIER | c.-177+12448G>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145494486 | |||||||
| chr4:145494493 | G | A | 1 | a0001c0001t0002g0209 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.-177+12455G>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145494493 | |||||||
| chr4:145494660 | A | G | 1 | a0001c0001t0002g0191 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.-177+12622A>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145494660 | |||||||
| chr4:145494679 | G | A | 2 | a0001c0001t0001g0066 a0001c0001t0001g0067 |
2 | HG02451.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.-177+12641G>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145494679 | |||||||
| chr4:145494783 | T | C | 7 | a0001c0001t0001g0033 a0001c0001t0009g0006 a0001c0001t0009g0023 others(4): Show |
8 | HG01261.hp1 HG02630.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.-177+12745T>C | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145494783 | |||||||
| chr4:145494936 | A | G | 1 | a0001c0001t0004g0014 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-177+12898A>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145494936 | |||||||
| chr4:145494983 | C | T | 2 | a0001c0001t0001g0043 a0001c0001t0001g0071 |
2 | HG02145.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.-177+12945C>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145494983 | |||||||
| chr4:145494990 | T | A | 1 | a0001c0001t0002g0165 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.-177+12952T>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145494990 | |||||||
| chr4:145495078 | G | A | 2 | a0001c0001t0001g0043 a0001c0001t0001g0071 |
2 | HG02145.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.-177+13040G>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145495078 | |||||||
| chr4:145495116 | G | A | 9 | a0001c0001t0007g0280 a0001c0001t0008g0020 a0001c0001t0008g0053 others(6): Show |
11 | HG01192.hp2 HG01496.hp2 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.-177+13078G>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145495116 | |||||||
| chr4:145495134 | G | A | 48 | a0001c0001t0001g0033 a0001c0001t0001g0146 a0001c0001t0004g0149 others(45): Show |
51 | HG00438.hp1 HG01192.hp2 HG01243.hp1 others(48): Show |
intron_variant | MODIFIER | c.-177+13096G>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145495134 | |||||||
| chr4:145495206 | G | A | 1 | a0001c0001t0001g0260 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.-177+13168G>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145495206 | |||||||
| chr4:145495253 | G | A | 166 | a0001c0001t0001g0033 a0001c0001t0001g0043 a0001c0001t0001g0054 others(163): Show |
178 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(175): Show |
intron_variant | MODIFIER | c.-177+13215G>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145495253 | |||||||
| chr4:145495257 | C | G | 2 | a0001c0001t0001g0043 a0001c0001t0001g0071 |
2 | HG02145.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.-177+13219C>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145495257 | |||||||
| chr4:145495279 | G | A | 4 | a0001c0001t0011g0005 a0001c0001t0011g0073 a0001c0001t0011g0074 others(1): Show |
5 | HG02559.hp1 HG02647.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.-177+13241G>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145495279 | |||||||
| chr4:145495298 | A | G | 3 | a0001c0002t0012g0052 a0001c0002t0012g0069 a0001c0002t0012g0143 |
3 | HG02145.hp1 HG02257.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.-177+13260A>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145495298 | |||||||
| chr4:145495341 | A | G | 4 | a0001c0001t0004g0149 a0001c0001t0004g0150 a0001c0001t0004g0151 others(1): Show |
4 | HG01243.hp1 HG02258.hp2 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.-177+13303A>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145495341 | |||||||
| chr4:145495383 | A | G | 24 | a0001c0001t0001g0138 a0001c0001t0001g0139 a0001c0001t0001g0141 others(21): Show |
26 | HG00423.hp2 HG00621.hp1 HG01081.hp1 others(23): Show |
intron_variant | MODIFIER | c.-177+13345A>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145495383 | |||||||
| chr4:145495450 | G | C | 1 | a0001c0002t0012g0143 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-177+13412G>C | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145495450 | |||||||
| chr4:145495459 | T | C | 15 | a0001c0001t0002g0001 a0001c0001t0002g0065 a0001c0001t0002g0081 others(12): Show |
18 | HG00408.hp2 HG00544.hp2 HG01167.hp1 others(15): Show |
intron_variant | MODIFIER | c.-177+13421T>C | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145495459 | |||||||
| chr4:145495492 | C | T | 2 | a0001c0001t0001g0043 a0001c0001t0001g0071 |
2 | HG02145.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.-177+13454C>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145495492 | |||||||
| chr4:145495537 | G | A | 9 | a0001c0001t0007g0280 a0001c0001t0008g0020 a0001c0001t0008g0053 others(6): Show |
11 | HG01192.hp2 HG01496.hp2 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.-177+13499G>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145495537 | |||||||
| chr4:145495616 | C | CT | 16 | a0001c0001t0001g0043 a0001c0001t0004g0106 a0001c0001t0006g0220 others(13): Show |
18 | HG01192.hp2 HG01496.hp2 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.-177+13597dupT | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr4 | 145495616 | ||||||
| chr4:145495616 | C | CTT | 31 | a0001c0001t0001g0033 a0001c0001t0001g0146 a0001c0001t0004g0149 others(28): Show |
32 | HG00438.hp1 HG01243.hp1 HG01243.hp2 others(29): Show |
intron_variant | MODIFIER | c.-177+13596_-177+13 others(8): Show |
SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr4 | 145495616 | ||||||
| chr4:145495701 | G | A | 8 | a0001c0001t0001g0146 a0001c0001t0004g0149 a0001c0001t0004g0150 others(5): Show |
8 | HG01243.hp1 HG02258.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.-177+13663G>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145495701 | |||||||
| chr4:145495779 | C | CT | 12 | a0001c0001t0002g0084 a0001c0001t0006g0119 a0001c0001t0006g0120 others(9): Show |
12 | HG00738.hp2 HG01081.hp2 HG03654.hp1 others(9): Show |
intron_variant | MODIFIER | c.-177+13760dupT | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr4 | 145495779 | ||||||
| chr4:145495779 | C | CTTTTT | 44 | a0001c0001t0001g0033 a0001c0001t0001g0043 a0001c0001t0001g0071 others(41): Show |
47 | HG00438.hp1 HG01192.hp2 HG01243.hp1 others(44): Show |
intron_variant | MODIFIER | c.-177+13756_-177+13 others(11): Show |
SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr4 | 145495779 | ||||||
| chr4:145495779 | C | CTTTTTT | 9 | a0001c0001t0005g0030 a0001c0001t0005g0051 a0001c0001t0005g0107 others(6): Show |
9 | HG02040.hp1 HG02135.hp2 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.-177+13755_-177+13 others(12): Show |
SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr4 | 145495779 | ||||||
| chr4:145495881 | A | G | 2 | a0001c0001t0018g0077 a0001c0001t0018g0153 |
2 | HG02895.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-177+13843A>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145495881 | |||||||
| chr4:145495984 | A | G | 1 | a0001c0001t0001g0190 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.-177+13946A>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145495984 | |||||||
| chr4:145495998 | A | G | 2 | a0001c0001t0001g0043 a0001c0001t0001g0071 |
2 | HG02145.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.-177+13960A>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145495998 | |||||||
| chr4:145496085 | A | T | 57 | a0001c0001t0001g0033 a0001c0001t0001g0043 a0001c0001t0001g0071 others(54): Show |
61 | HG00438.hp1 HG01192.hp2 HG01243.hp1 others(58): Show |
intron_variant | MODIFIER | c.-177+14047A>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145496085 | |||||||
| chr4:145496164 | A | G | 1 | a0001c0001t0004g0152 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-177+14126A>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145496164 | |||||||
| chr4:145496276 | G | C | 1 | a0001c0001t0001g0173 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.-177+14238G>C | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145496276 | |||||||
| chr4:145496357 | A | G | 2 | a0001c0001t0001g0043 a0001c0001t0001g0071 |
2 | HG02145.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.-177+14319A>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145496357 | |||||||
| chr4:145496481 | T | A | 3 | a0001c0001t0005g0027 a0001c0001t0005g0028 a0001c0001t0005g0047 |
3 | HG01884.hp2 HG03130.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.-177+14443T>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145496481 | |||||||
| chr4:145496545 | G | T | 56 | a0001c0001t0001g0043 a0001c0001t0001g0071 a0001c0001t0001g0146 others(53): Show |
60 | HG00438.hp1 HG01192.hp2 HG01243.hp1 others(57): Show |
intron_variant | MODIFIER | c.-177+14507G>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145496545 | |||||||
| chr4:145496620 | T | C | 56 | a0001c0001t0001g0043 a0001c0001t0001g0071 a0001c0001t0001g0146 others(53): Show |
60 | HG00438.hp1 HG01192.hp2 HG01243.hp1 others(57): Show |
intron_variant | MODIFIER | c.-177+14582T>C | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145496620 | |||||||
| chr4:145496954 | A | G | 1 | a0001c0001t0001g0141 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.-177+14916A>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145496954 | |||||||
| chr4:145497015 | A | G | 56 | a0001c0001t0001g0043 a0001c0001t0001g0071 a0001c0001t0001g0146 others(53): Show |
60 | HG00438.hp1 HG01192.hp2 HG01243.hp1 others(57): Show |
intron_variant | MODIFIER | c.-177+14977A>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145497015 | |||||||
| chr4:145497036 | A | G | 1 | a0001c0001t0004g0116 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.-177+14998A>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145497036 | |||||||
| chr4:145497242 | A | T | 1 | a0001c0001t0027g0142 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-177+15204A>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145497242 | |||||||
| chr4:145497274 | T | G | 2 | a0001c0001t0018g0077 a0001c0001t0018g0153 |
2 | HG02895.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-177+15236T>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145497274 | |||||||
| chr4:145497295 | T | C | 1 | a0001c0001t0003g0235 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.-177+15257T>C | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145497295 | |||||||
| chr4:145497368 | G | A | 5 | a0001c0001t0008g0020 a0001c0001t0008g0053 a0001c0001t0008g0155 others(2): Show |
6 | HG01192.hp2 HG01496.hp2 HG01891.hp2 others(3): Show |
intron_variant | MODIFIER | c.-177+15330G>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145497368 | |||||||
| chr4:145497379 | C | T | 1 | a0001c0001t0002g0274 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.-177+15341C>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145497379 | |||||||
| chr4:145497403 | G | C | 56 | a0001c0001t0001g0043 a0001c0001t0001g0071 a0001c0001t0001g0146 others(53): Show |
60 | HG00438.hp1 HG01192.hp2 HG01243.hp1 others(57): Show |
intron_variant | MODIFIER | c.-177+15365G>C | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145497403 | |||||||
| chr4:145497635 | C | T | 3 | a0001c0002t0012g0052 a0001c0002t0012g0069 a0001c0002t0012g0143 |
3 | HG02145.hp1 HG02257.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.-177+15597C>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145497635 | |||||||
| chr4:145497649 | T | C | 1 | a0001c0001t0001g0259 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-177+15611T>C | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145497649 | |||||||
| chr4:145497695 | T | C | 168 | a0001c0001t0001g0009 a0001c0001t0001g0038 a0001c0001t0001g0043 others(165): Show |
181 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(178): Show |
intron_variant | MODIFIER | c.-177+15657T>C | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145497695 | |||||||
| chr4:145497747 | C | G | 2 | a0001c0001t0001g0043 a0001c0001t0001g0071 |
2 | HG02145.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.-177+15709C>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145497747 | |||||||
| chr4:145497771 | T | G | 2 | a0001c0001t0008g0031 a0001c0001t0008g0032 |
2 | HG02976.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-177+15733T>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145497771 | |||||||
| chr4:145497870 | G | A | 4 | a0001c0001t0011g0005 a0001c0001t0011g0073 a0001c0001t0011g0074 others(1): Show |
5 | HG02559.hp1 HG02647.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.-177+15832G>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145497870 | |||||||
| chr4:145497883 | A | G | 5 | a0001c0001t0008g0020 a0001c0001t0008g0053 a0001c0001t0008g0155 others(2): Show |
6 | HG01192.hp2 HG01496.hp2 HG01891.hp2 others(3): Show |
intron_variant | MODIFIER | c.-177+15845A>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145497883 | |||||||
| chr4:145498035 | T | A | 2 | a0001c0001t0001g0043 a0001c0001t0001g0071 |
2 | HG02145.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.-177+15997T>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145498035 | |||||||
| chr4:145498245 | C | T | 1 | a0001c0001t0001g0270 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-176-16193C>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145498245 | |||||||
| chr4:145498928 | C | A | 9 | a0001c0001t0001g0043 a0001c0001t0001g0071 a0001c0001t0011g0005 others(6): Show |
10 | HG01884.hp1 HG02109.hp2 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.-176-15510C>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145498928 | |||||||
| chr4:145499093 | T | C | 47 | a0001c0001t0001g0146 a0001c0001t0004g0149 a0001c0001t0004g0150 others(44): Show |
50 | HG00438.hp1 HG01192.hp2 HG01243.hp1 others(47): Show |
intron_variant | MODIFIER | c.-176-15345T>C | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145499093 | |||||||
| chr4:145499186 | G | A | 4 | a0001c0001t0007g0280 a0001c0001t0015g0011 a0001c0001t0015g0161 others(1): Show |
5 | HG02055.hp2 HG02280.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.-176-15252G>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145499186 | |||||||
| chr4:145499348 | C | G | 9 | a0001c0001t0007g0280 a0001c0001t0008g0020 a0001c0001t0008g0053 others(6): Show |
11 | HG01192.hp2 HG01496.hp2 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.-176-15090C>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145499348 | |||||||
| chr4:145499355 | G | A | 4 | a0001c0001t0011g0005 a0001c0001t0011g0073 a0001c0001t0011g0074 others(1): Show |
5 | HG02559.hp1 HG02647.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.-176-15083G>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145499355 | |||||||
| chr4:145499424 | C | G | 2 | a0001c0003t0012g0072 a0001c0003t0012g0144 |
2 | HG01884.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.-176-15014C>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145499424 | |||||||
| chr4:145499436 | T | A | 2 | a0001c0003t0012g0072 a0001c0003t0012g0144 |
2 | HG01884.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.-176-15002T>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145499436 | |||||||
| chr4:145499715 | T | G | 3 | a0001c0002t0012g0052 a0001c0002t0012g0069 a0001c0002t0012g0143 |
3 | HG02145.hp1 HG02257.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.-176-14723T>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145499715 | |||||||
| chr4:145499843 | A | G | 3 | a0001c0001t0015g0011 a0001c0001t0015g0161 a0001c0001t0027g0142 |
4 | HG02055.hp2 HG02280.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.-176-14595A>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145499843 | |||||||
| chr4:145499933 | G | A | 56 | a0001c0001t0001g0043 a0001c0001t0001g0071 a0001c0001t0001g0146 others(53): Show |
60 | HG00438.hp1 HG01192.hp2 HG01243.hp1 others(57): Show |
intron_variant | MODIFIER | c.-176-14505G>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145499933 | |||||||
| chr4:145499995 | A | C | 3 | a0001c0001t0007g0280 a0001c0001t0018g0077 a0001c0001t0018g0153 |
3 | HG02895.hp1 HG03540.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-176-14443A>C | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145499995 | |||||||
| chr4:145500335 | C | T | 2 | a0001c0001t0018g0077 a0001c0001t0018g0153 |
2 | HG02895.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-176-14103C>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145500335 | |||||||
| chr4:145500380 | C | A | 1 | a0001c0001t0003g0018 | 2 | HG00642.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.-176-14058C>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145500380 | |||||||
| chr4:145500412 | G | A | 1 | a0001c0002t0030g0075 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-176-14026G>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145500412 | |||||||
| chr4:145500531 | C | T | 1 | a0001c0002t0030g0075 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-176-13907C>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145500531 | |||||||
| chr4:145500550 | A | G | 96 | a0001c0001t0001g0043 a0001c0001t0001g0054 a0001c0001t0001g0066 others(93): Show |
101 | HG00423.hp2 HG00438.hp1 HG00621.hp1 others(98): Show |
intron_variant | MODIFIER | c.-176-13888A>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145500550 | |||||||
| chr4:145500552 | G | A | 5 | a0001c0001t0001g0101 a0001c0001t0001g0200 a0001c0001t0004g0201 others(2): Show |
5 | HG02717.hp1 HG02809.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.-176-13886G>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145500552 | |||||||
| chr4:145500555 | G | A | 2 | a0001c0001t0008g0031 a0001c0001t0008g0032 |
2 | HG02976.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-176-13883G>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145500555 | |||||||
| chr4:145500716 | T | G | 1 | a0001c0001t0004g0055 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-176-13722T>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145500716 | |||||||
| chr4:145500984 | G | A | 4 | a0001c0001t0011g0005 a0001c0001t0011g0073 a0001c0001t0011g0074 others(1): Show |
5 | HG02559.hp1 HG02647.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.-176-13454G>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145500984 | |||||||
| chr4:145501021 | G | A | 3 | a0001c0002t0012g0052 a0001c0002t0012g0069 a0001c0002t0012g0143 |
3 | HG02145.hp1 HG02257.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.-176-13417G>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145501021 | |||||||
| chr4:145501514 | G | A | 2 | a0001c0001t0008g0031 a0001c0001t0008g0032 |
2 | HG02976.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-176-12924G>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145501514 | |||||||
| chr4:145501533 | A | G | 77 | a0001c0001t0001g0054 a0001c0001t0001g0066 a0001c0001t0001g0067 others(74): Show |
81 | HG00423.hp2 HG00438.hp1 HG00621.hp1 others(78): Show |
intron_variant | MODIFIER | c.-176-12905A>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145501533 | |||||||
| chr4:145501552 | G | A | 2 | a0001c0003t0012g0072 a0001c0003t0012g0144 |
2 | HG01884.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.-176-12886G>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145501552 | |||||||
| chr4:145501641 | CT | C | 88 | a0001c0001t0001g0054 a0001c0001t0001g0066 a0001c0001t0001g0067 others(85): Show |
95 | HG00423.hp2 HG00438.hp1 HG00621.hp1 others(92): Show |
intron_variant | MODIFIER | c.-176-12784delT | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr4 | 145501641 | ||||||
| chr4:145501721 | CT | C | 53 | a0001c0001t0001g0243 a0001c0001t0003g0004 a0001c0001t0003g0016 others(50): Show |
58 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(55): Show |
intron_variant | MODIFIER | c.-176-12705delT | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr4 | 145501721 | ||||||
| chr4:145501881 | C | G | 165 | a0001c0001t0001g0043 a0001c0001t0001g0054 a0001c0001t0001g0066 others(162): Show |
177 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(174): Show |
intron_variant | MODIFIER | c.-176-12557C>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145501881 | |||||||
| chr4:145501989 | C | T | 2 | a0001c0001t0001g0043 a0001c0001t0001g0071 |
2 | HG02145.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.-176-12449C>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145501989 | |||||||
| chr4:145502065 | C | T | 2 | a0001c0001t0001g0043 a0001c0001t0001g0071 |
2 | HG02145.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.-176-12373C>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145502065 | |||||||
| chr4:145502123 | A | G | 1 | a0001c0001t0027g0142 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-176-12315A>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145502123 | |||||||
| chr4:145502229 | G | C | 3 | a0001c0001t0003g0135 a0001c0001t0003g0252 a0001c0001t0007g0251 |
3 | HG01175.hp2 HG01257.hp1 HG02148.hp2 |
intron_variant | MODIFIER | c.-176-12209G>C | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145502229 | |||||||
| chr4:145502246 | A | G | 100 | a0001c0001t0001g0043 a0001c0001t0001g0054 a0001c0001t0001g0066 others(97): Show |
107 | HG00423.hp2 HG00438.hp1 HG00621.hp1 others(104): Show |
intron_variant | MODIFIER | c.-176-12192A>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145502246 | |||||||
| chr4:145502267 | C | T | 15 | a0001c0001t0001g0043 a0001c0001t0001g0071 a0001c0001t0007g0280 others(12): Show |
18 | HG01192.hp2 HG01496.hp2 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.-176-12171C>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145502267 | |||||||
| chr4:145502363 | T | G | 100 | a0001c0001t0001g0043 a0001c0001t0001g0054 a0001c0001t0001g0066 others(97): Show |
107 | HG00423.hp2 HG00438.hp1 HG00621.hp1 others(104): Show |
intron_variant | MODIFIER | c.-176-12075T>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145502363 | |||||||
| chr4:145502399 | A | T | 2 | a0001c0001t0001g0043 a0001c0001t0001g0071 |
2 | HG02145.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.-176-12039A>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145502399 | |||||||
| chr4:145502427 | A | G | 4 | a0001c0001t0011g0005 a0001c0001t0011g0073 a0001c0001t0011g0074 others(1): Show |
5 | HG02559.hp1 HG02647.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.-176-12011A>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145502427 | |||||||
| chr4:145502534 | A | G | 1 | a0001c0001t0004g0105 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-176-11904A>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145502534 | |||||||
| chr4:145502628 | A | G | 1 | a0001c0001t0007g0280 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-176-11810A>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145502628 | |||||||
| chr4:145502649 | C | T | 1 | a0001c0001t0001g0071 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-176-11789C>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145502649 | |||||||
| chr4:145502775 | A | T | 2 | a0001c0001t0002g0096 a0001c0001t0002g0189 |
2 | HG00099.hp2 HG01099.hp2 |
intron_variant | MODIFIER | c.-176-11663A>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145502775 | |||||||
| chr4:145502823 | A | G | 27 | a0001c0001t0004g0149 a0001c0001t0004g0150 a0001c0001t0004g0151 others(24): Show |
28 | HG00438.hp1 HG01243.hp1 HG01243.hp2 others(25): Show |
intron_variant | MODIFIER | c.-176-11615A>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145502823 | |||||||
| chr4:145502837 | G | A | 1 | a0001c0001t0001g0174 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.-176-11601G>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145502837 | |||||||
| chr4:145502912 | G | A | 1 | a0001c0002t0030g0075 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-176-11526G>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145502912 | |||||||
| chr4:145502956 | TCAGTGTC others(15): Show |
T | 1 | a0001c0001t0002g0172 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.-176-11463_-176-11 others(28): Show |
SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr4 | 145502956 | ||||||
| chr4:145502989 | G | A | 2 | a0001c0001t0018g0077 a0001c0001t0018g0153 |
2 | HG02895.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-176-11449G>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145502989 | |||||||
| chr4:145503403 | C | T | 2 | a0001c0001t0018g0077 a0001c0001t0018g0153 |
2 | HG02895.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-176-11035C>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145503403 | |||||||
| chr4:145503422 | C | T | 12 | a0001c0001t0006g0119 a0001c0001t0006g0120 a0001c0001t0006g0121 others(9): Show |
12 | HG00738.hp2 HG01081.hp2 HG03654.hp1 others(9): Show |
intron_variant | MODIFIER | c.-176-11016C>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145503422 | |||||||
| chr4:145503677 | A | G | 3 | a0001c0001t0006g0217 a0001c0001t0006g0218 a0001c0001t0006g0219 |
3 | HG01081.hp2 HG03942.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.-176-10761A>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145503677 | |||||||
| chr4:145504071 | C | T | 8 | a0001c0001t0018g0077 a0001c0001t0018g0153 a0001c0002t0012g0052 others(5): Show |
8 | HG01884.hp1 HG02109.hp2 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.-176-10367C>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145504071 | |||||||
| chr4:145504238 | T | C | 1 | a0001c0001t0023g0208 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.-176-10200T>C | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145504238 | |||||||
| chr4:145504303 | A | G | 1 | a0001c0001t0001g0156 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.-176-10135A>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145504303 | |||||||
| chr4:145504391 | C | A | 2 | a0001c0001t0003g0016 a0001c0001t0003g0137 |
3 | HG01099.hp1 HG01255.hp2 HG01358.hp2 |
intron_variant | MODIFIER | c.-176-10047C>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145504391 | |||||||
| chr4:145504453 | C | T | 4 | a0001c0001t0011g0005 a0001c0001t0011g0073 a0001c0001t0011g0074 others(1): Show |
5 | HG02559.hp1 HG02647.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.-176-9985C>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145504453 | |||||||
| chr4:145504464 | G | A | 1 | a0001c0001t0003g0276 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.-176-9974G>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145504464 | |||||||
| chr4:145504467 | C | T | 16 | a0001c0001t0005g0024 a0001c0001t0005g0025 a0001c0001t0005g0026 others(13): Show |
16 | HG00438.hp1 HG01243.hp2 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.-176-9971C>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145504467 | |||||||
| chr4:145504528 | G | A | 3 | a0001c0002t0012g0052 a0001c0002t0012g0069 a0001c0002t0012g0143 |
3 | HG02145.hp1 HG02257.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.-176-9910G>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145504528 | |||||||
| chr4:145504671 | T | A | 4 | a0001c0001t0001g0043 a0001c0001t0001g0066 a0001c0001t0001g0067 others(1): Show |
4 | HG02145.hp2 HG02451.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.-176-9767T>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145504671 | |||||||
| chr4:145504748 | T | G | 1 | a0001c0001t0028g0278 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.-176-9690T>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145504748 | |||||||
| chr4:145504841 | C | T | 6 | a0001c0002t0012g0052 a0001c0002t0012g0069 a0001c0002t0012g0143 others(3): Show |
6 | HG01884.hp1 HG02109.hp2 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.-176-9597C>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145504841 | |||||||
| chr4:145504862 | C | G | 1 | a0001c0001t0001g0022 | 2 | HG01928.hp1 HG02293.hp2 |
intron_variant | MODIFIER | c.-176-9576C>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145504862 | |||||||
| chr4:145504949 | G | A | 1 | a0001c0001t0004g0117 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-176-9489G>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145504949 | |||||||
| chr4:145504955 | C | G | 85 | a0001c0001t0001g0009 a0001c0001t0001g0038 a0001c0001t0001g0054 others(82): Show |
90 | HG00423.hp2 HG00438.hp1 HG00621.hp1 others(87): Show |
intron_variant | MODIFIER | c.-176-9483C>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145504955 | |||||||
| chr4:145504990 | G | A | 6 | a0001c0002t0012g0052 a0001c0002t0012g0069 a0001c0002t0012g0143 others(3): Show |
6 | HG01884.hp1 HG02109.hp2 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.-176-9448G>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145504990 | |||||||
| chr4:145505048 | A | G | 1 | a0001c0001t0004g0115 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-176-9390A>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145505048 | |||||||
| chr4:145505056 | T | C | 1 | a0001c0001t0001g0210 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.-176-9382T>C | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145505056 | |||||||
| chr4:145505162 | T | C | 53 | a0001c0001t0001g0243 a0001c0001t0003g0004 a0001c0001t0003g0016 others(50): Show |
58 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(55): Show |
intron_variant | MODIFIER | c.-176-9276T>C | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145505162 | |||||||
| chr4:145505174 | T | C | 1 | a0001c0001t0007g0227 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.-176-9264T>C | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145505174 | |||||||
| chr4:145505198 | C | T | 3 | a0001c0002t0012g0052 a0001c0002t0012g0069 a0001c0002t0012g0143 |
3 | HG02145.hp1 HG02257.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.-176-9240C>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145505198 | |||||||
| chr4:145505367 | T | C | 1 | a0001c0001t0001g0258 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.-176-9071T>C | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145505367 | |||||||
| chr4:145505575 | C | T | 1 | a0001c0001t0001g0188 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.-176-8863C>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145505575 | |||||||
| chr4:145505610 | C | G | 1 | a0001c0001t0001g0190 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.-176-8828C>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145505610 | |||||||
| chr4:145505616 | C | CA | 14 | a0001c0001t0001g0043 a0001c0001t0001g0066 a0001c0001t0001g0067 others(11): Show |
14 | HG01433.hp1 HG01934.hp2 HG01981.hp1 others(11): Show |
intron_variant | MODIFIER | c.-176-8805dupA | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr4 | 145505616 | ||||||
| chr4:145505616 | CA | C | 38 | a0001c0001t0001g0205 a0001c0001t0004g0007 a0001c0001t0004g0110 others(35): Show |
41 | HG00423.hp2 HG00438.hp1 HG01243.hp1 others(38): Show |
intron_variant | MODIFIER | c.-176-8805delA | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr4 | 145505616 | ||||||
| chr4:145505616 | CAA | C | 46 | a0001c0001t0001g0054 a0001c0001t0001g0078 a0001c0001t0001g0122 others(43): Show |
48 | HG00621.hp1 HG01081.hp1 HG01175.hp1 others(45): Show |
intron_variant | MODIFIER | c.-176-8806_-176-880 others(6): Show |
SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr4 | 145505616 | ||||||
| chr4:145505626 | A | G | 2 | a0001c0001t0017g0214 a0001c0001t0025g0273 |
2 | HG03927.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.-176-8812A>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145505626 | |||||||
| chr4:145505675 | T | G | 1 | a0001c0001t0001g0159 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.-176-8763T>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145505675 | |||||||
| chr4:145505767 | G | A | 2 | a0001c0001t0002g0012 a0001c0001t0002g0175 |
3 | NA18960.hp1 NA18975.hp1 NA18990.hp1 |
intron_variant | MODIFIER | c.-176-8671G>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145505767 | |||||||
| chr4:145505792 | A | G | 2 | a0001c0003t0012g0072 a0001c0003t0012g0144 |
2 | HG01884.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.-176-8646A>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145505792 | |||||||
| chr4:145505796 | G | A | 3 | a0001c0002t0012g0052 a0001c0002t0012g0069 a0001c0002t0012g0143 |
3 | HG02145.hp1 HG02257.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.-176-8642G>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145505796 | |||||||
| chr4:145505879 | C | T | 1 | a0001c0002t0030g0075 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-176-8559C>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145505879 | |||||||
| chr4:145505932 | C | T | 2 | a0001c0003t0012g0072 a0001c0003t0012g0144 |
2 | HG01884.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.-176-8506C>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145505932 | |||||||
| chr4:145506259 | T | C | 1 | a0001c0002t0030g0075 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-176-8179T>C | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145506259 | |||||||
| chr4:145506399 | C | T | 75 | a0001c0001t0001g0054 a0001c0001t0001g0078 a0001c0001t0001g0122 others(72): Show |
79 | HG00423.hp2 HG00438.hp1 HG00621.hp1 others(76): Show |
intron_variant | MODIFIER | c.-176-8039C>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145506399 | |||||||
| chr4:145506689 | T | TA | 5 | a0001c0001t0002g0084 a0001c0001t0009g0034 a0001c0001t0009g0154 others(2): Show |
5 | HG01261.hp1 HG02630.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.-176-7740dupA | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr4 | 145506689 | ||||||
| chr4:145506730 | T | C | 3 | a0001c0002t0012g0052 a0001c0002t0012g0069 a0001c0002t0012g0143 |
3 | HG02145.hp1 HG02257.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.-176-7708T>C | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145506730 | |||||||
| chr4:145506957 | C | T | 3 | a0001c0002t0012g0052 a0001c0002t0012g0069 a0001c0002t0012g0143 |
3 | HG02145.hp1 HG02257.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.-176-7481C>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145506957 | |||||||
| chr4:145506965 | A | G | 1 | a0001c0001t0004g0105 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-176-7473A>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145506965 | |||||||
| chr4:145506965 | A | T | 4 | a0001c0001t0005g0025 a0001c0001t0005g0045 a0001c0001t0005g0046 others(1): Show |
4 | HG00438.hp1 HG02135.hp2 NA18964.hp2 others(1): Show |
intron_variant | MODIFIER | c.-176-7473A>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145506965 | |||||||
| chr4:145507068 | A | G | 5 | a0001c0001t0003g0127 a0001c0001t0003g0232 a0001c0001t0003g0233 others(2): Show |
5 | HG00438.hp2 NA19057.hp1 NA19065.hp2 others(2): Show |
intron_variant | MODIFIER | c.-176-7370A>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145507068 | |||||||
| chr4:145507134 | G | C | 1 | a0001c0001t0007g0229 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.-176-7304G>C | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145507134 | |||||||
| chr4:145507175 | G | GT | 18 | a0001c0001t0002g0084 a0001c0001t0004g0112 a0001c0001t0006g0119 others(15): Show |
19 | HG00738.hp2 HG01081.hp2 HG02895.hp1 others(16): Show |
intron_variant | MODIFIER | c.-176-7251dupT | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr4 | 145507175 | ||||||
| chr4:145507175 | G | T | 1 | a0001c0001t0004g0109 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.-176-7263G>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145507175 | |||||||
| chr4:145507176 | T | G | 2 | a0001c0001t0001g0066 a0001c0001t0001g0067 |
2 | HG02451.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.-176-7262T>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145507176 | |||||||
| chr4:145507232 | A | G | 221 | a0001c0001t0001g0009 a0001c0001t0001g0013 a0001c0001t0001g0021 others(218): Show |
237 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(234): Show |
intron_variant | MODIFIER | c.-176-7206A>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145507232 | |||||||
| chr4:145507369 | C | T | 1 | a0001c0001t0001g0058 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.-176-7069C>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145507369 | |||||||
| chr4:145507681 | T | C | 1 | a0001c0001t0003g0018 | 2 | HG00642.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.-176-6757T>C | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145507681 | |||||||
| chr4:145507979 | A | C | 2 | a0001c0001t0001g0009 a0001c0001t0001g0038 |
3 | HG02622.hp1 HG03209.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.-176-6459A>C | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145507979 | |||||||
| chr4:145508013 | TCG | T | 16 | a0001c0001t0005g0024 a0001c0001t0005g0025 a0001c0001t0005g0026 others(13): Show |
16 | HG00438.hp1 HG01243.hp2 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.-176-6424_-176-642 others(6): Show |
SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145508013 | |||||||
| chr4:145508065 | A | C | 1 | a0001c0001t0005g0044 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-176-6373A>C | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145508065 | |||||||
| chr4:145508080 | A | AT | 17 | a0001c0001t0001g0187 a0001c0001t0002g0084 a0001c0001t0002g0181 others(14): Show |
17 | HG00438.hp1 HG00738.hp2 HG01081.hp2 others(14): Show |
intron_variant | MODIFIER | c.-176-6341dupT | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr4 | 145508080 | ||||||
| chr4:145508080 | AT | A | 54 | a0001c0001t0001g0243 a0001c0001t0001g0264 a0001c0001t0003g0004 others(51): Show |
58 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(55): Show |
intron_variant | MODIFIER | c.-176-6341delT | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr4 | 145508080 | ||||||
| chr4:145508616 | G | C | 2 | a0001c0001t0018g0077 a0001c0001t0018g0153 |
2 | HG02895.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-176-5822G>C | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145508616 | |||||||
| chr4:145508640 | T | A | 11 | a0001c0001t0004g0149 a0001c0001t0004g0150 a0001c0001t0004g0151 others(8): Show |
12 | HG01243.hp1 HG01261.hp1 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.-176-5798T>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145508640 | |||||||
| chr4:145508804 | G | A | 1 | a0001c0001t0002g0176 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.-176-5634G>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145508804 | |||||||
| chr4:145508889 | T | C | 6 | a0001c0002t0012g0052 a0001c0002t0012g0069 a0001c0002t0012g0143 others(3): Show |
6 | HG01884.hp1 HG02109.hp2 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.-176-5549T>C | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145508889 | |||||||
| chr4:145508951 | C | G | 1 | a0001c0002t0030g0075 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-176-5487C>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145508951 | |||||||
| chr4:145509103 | C | T | 2 | a0001c0003t0012g0072 a0001c0003t0012g0144 |
2 | HG01884.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.-176-5335C>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145509103 | |||||||
| chr4:145509133 | T | G | 3 | a0001c0002t0012g0052 a0001c0002t0012g0069 a0001c0002t0012g0143 |
3 | HG02145.hp1 HG02257.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.-176-5305T>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145509133 | |||||||
| chr4:145509141 | T | G | 100 | a0001c0001t0001g0043 a0001c0001t0001g0054 a0001c0001t0001g0066 others(97): Show |
107 | HG00423.hp2 HG00438.hp1 HG00621.hp1 others(104): Show |
intron_variant | MODIFIER | c.-176-5297T>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145509141 | |||||||
| chr4:145509143 | A | G | 1 | a0001c0002t0030g0075 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-176-5295A>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145509143 | |||||||
| chr4:145509381 | C | T | 4 | a0001c0001t0007g0280 a0001c0001t0015g0011 a0001c0001t0015g0161 others(1): Show |
5 | HG02055.hp2 HG02280.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.-176-5057C>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145509381 | |||||||
| chr4:145509382 | G | A | 3 | a0001c0001t0004g0149 a0001c0001t0004g0150 a0001c0001t0004g0151 |
3 | HG02258.hp2 HG02280.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.-176-5056G>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145509382 | |||||||
| chr4:145509518 | C | T | 6 | a0001c0001t0009g0006 a0001c0001t0009g0023 a0001c0001t0009g0034 others(3): Show |
7 | HG01261.hp1 HG02630.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.-176-4920C>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145509518 | |||||||
| chr4:145509654 | G | A | 1 | a0001c0001t0001g0203 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-176-4784G>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145509654 | |||||||
| chr4:145509887 | C | T | 1 | a0001c0001t0013g0041 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-176-4551C>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145509887 | |||||||
| chr4:145509888 | G | A | 2 | a0001c0001t0005g0025 a0001c0001t0005g0046 |
2 | HG00438.hp1 NA18964.hp2 |
intron_variant | MODIFIER | c.-176-4550G>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145509888 | |||||||
| chr4:145509949 | G | T | 2 | a0001c0001t0002g0179 a0001c0001t0002g0180 |
2 | HG01261.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.-176-4489G>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145509949 | |||||||
| chr4:145510002 | A | G | 29 | a0001c0001t0001g0054 a0001c0001t0001g0078 a0001c0001t0001g0138 others(26): Show |
31 | HG00423.hp2 HG00621.hp1 HG01081.hp1 others(28): Show |
intron_variant | MODIFIER | c.-176-4436A>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145510002 | |||||||
| chr4:145510396 | A | G | 6 | a0001c0002t0012g0052 a0001c0002t0012g0069 a0001c0002t0012g0143 others(3): Show |
6 | HG01884.hp1 HG02109.hp2 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.-176-4042A>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145510396 | |||||||
| chr4:145510477 | T | C | 26 | a0001c0001t0001g0138 a0001c0001t0001g0139 a0001c0001t0001g0141 others(23): Show |
28 | HG00423.hp2 HG00621.hp1 HG01081.hp1 others(25): Show |
intron_variant | MODIFIER | c.-176-3961T>C | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145510477 | |||||||
| chr4:145510706 | T | G | 1 | a0001c0002t0030g0075 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-176-3732T>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145510706 | |||||||
| chr4:145510729 | G | C | 3 | a0001c0001t0002g0097 a0001c0001t0002g0192 a0001c0001t0002g0193 |
3 | NA18957.hp1 NA19002.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.-176-3709G>C | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145510729 | |||||||
| chr4:145511015 | C | T | 5 | a0001c0002t0012g0052 a0001c0002t0012g0069 a0001c0002t0012g0143 others(2): Show |
5 | HG01884.hp1 HG02109.hp2 HG02145.hp1 others(2): Show |
intron_variant | MODIFIER | c.-176-3423C>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145511015 | |||||||
| chr4:145511096 | T | C | 4 | a0001c0001t0004g0008 a0001c0001t0004g0117 a0001c0001t0004g0118 others(1): Show |
5 | HG02602.hp2 HG03017.hp1 HG03654.hp2 others(2): Show |
intron_variant | MODIFIER | c.-176-3342T>C | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145511096 | |||||||
| chr4:145511194 | T | C | 4 | a0001c0001t0011g0005 a0001c0001t0011g0073 a0001c0001t0011g0074 others(1): Show |
5 | HG02559.hp1 HG02647.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.-176-3244T>C | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145511194 | |||||||
| chr4:145511302 | C | CA | 102 | a0001c0001t0001g0009 a0001c0001t0001g0038 a0001c0001t0001g0043 others(99): Show |
110 | HG00423.hp2 HG00438.hp1 HG00621.hp1 others(107): Show |
intron_variant | MODIFIER | c.-176-3136_-176-313 others(5): Show |
SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145511302 | |||||||
| chr4:145511303 | G | T | 1 | a0001c0001t0003g0234 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.-176-3135G>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145511303 | |||||||
| chr4:145511342 | A | G | 4 | a0001c0001t0011g0005 a0001c0001t0011g0073 a0001c0001t0011g0074 others(1): Show |
5 | HG02559.hp1 HG02647.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.-176-3096A>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145511342 | |||||||
| chr4:145511692 | C | T | 1 | a0001c0001t0002g0100 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.-176-2746C>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145511692 | |||||||
| chr4:145511884 | T | C | 4 | a0001c0001t0001g0043 a0001c0001t0001g0066 a0001c0001t0001g0067 others(1): Show |
4 | HG02145.hp2 HG02451.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.-176-2554T>C | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145511884 | |||||||
| chr4:145511928 | T | C | 1 | a0001c0001t0003g0234 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.-176-2510T>C | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145511928 | |||||||
| chr4:145511935 | T | C | 4 | a0001c0001t0001g0043 a0001c0001t0001g0066 a0001c0001t0001g0067 others(1): Show |
4 | HG02145.hp2 HG02451.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.-176-2503T>C | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145511935 | |||||||
| chr4:145512059 | C | T | 4 | a0001c0001t0001g0043 a0001c0001t0001g0066 a0001c0001t0001g0067 others(1): Show |
4 | HG02145.hp2 HG02451.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.-176-2379C>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145512059 | |||||||
| chr4:145512081 | T | C | 1 | a0001c0001t0007g0280 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-176-2357T>C | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145512081 | |||||||
| chr4:145512263 | C | T | 1 | a0001c0001t0004g0055 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-176-2175C>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145512263 | |||||||
| chr4:145512364 | C | T | 77 | a0001c0001t0001g0009 a0001c0001t0001g0038 a0001c0001t0001g0054 others(74): Show |
82 | HG00423.hp2 HG00438.hp1 HG00621.hp1 others(79): Show |
intron_variant | MODIFIER | c.-176-2074C>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145512364 | |||||||
| chr4:145512634 | C | T | 4 | a0001c0001t0001g0122 a0001c0001t0001g0223 a0001c0001t0001g0224 others(1): Show |
4 | HG01891.hp1 HG03041.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.-176-1804C>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145512634 | |||||||
| chr4:145512665 | T | G | 2 | a0001c0001t0018g0077 a0001c0001t0018g0153 |
2 | HG02895.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-176-1773T>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145512665 | |||||||
| chr4:145512928 | G | T | 4 | a0001c0001t0011g0005 a0001c0001t0011g0073 a0001c0001t0011g0074 others(1): Show |
5 | HG02559.hp1 HG02647.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.-176-1510G>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145512928 | |||||||
| chr4:145512940 | C | A | 1 | a0001c0001t0007g0092 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.-176-1498C>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145512940 | |||||||
| chr4:145513046 | G | A | 46 | a0001c0001t0001g0054 a0001c0001t0001g0078 a0001c0001t0001g0122 others(43): Show |
49 | HG00423.hp2 HG00621.hp1 HG01081.hp1 others(46): Show |
intron_variant | MODIFIER | c.-176-1392G>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145513046 | |||||||
| chr4:145513077 | C | T | 16 | a0001c0001t0005g0024 a0001c0001t0005g0025 a0001c0001t0005g0026 others(13): Show |
16 | HG00438.hp1 HG01243.hp2 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.-176-1361C>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145513077 | |||||||
| chr4:145513200 | C | T | 1 | a0001c0001t0014g0148 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-176-1238C>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145513200 | |||||||
| chr4:145513528 | C | T | 46 | a0001c0001t0001g0054 a0001c0001t0001g0078 a0001c0001t0001g0122 others(43): Show |
49 | HG00423.hp2 HG00621.hp1 HG01081.hp1 others(46): Show |
intron_variant | MODIFIER | c.-176-910C>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145513528 | |||||||
| chr4:145513550 | T | A | 2 | a0001c0001t0008g0031 a0001c0001t0008g0032 |
2 | HG02976.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-176-888T>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145513550 | |||||||
| chr4:145513634 | G | T | 8 | a0001c0001t0018g0077 a0001c0001t0018g0153 a0001c0002t0012g0052 others(5): Show |
8 | HG01884.hp1 HG02109.hp2 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.-176-804G>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145513634 | |||||||
| chr4:145513911 | T | C | 2 | a0001c0003t0012g0072 a0001c0003t0012g0144 |
2 | HG01884.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.-176-527T>C | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145513911 | |||||||
| chr4:145513914 | T | A | 2 | a0001c0003t0012g0072 a0001c0003t0012g0144 |
2 | HG01884.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.-176-524T>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145513914 | |||||||
| chr4:145514222 | TACTTA | T | 75 | a0001c0001t0001g0054 a0001c0001t0001g0078 a0001c0001t0001g0122 others(72): Show |
79 | HG00423.hp2 HG00438.hp1 HG00621.hp1 others(76): Show |
intron_variant | MODIFIER | c.-176-211_-176-207d others(7): Show |
SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr4 | 145514222 | ||||||
| chr4:145515090 | C | A | 6 | a0001c0002t0012g0052 a0001c0002t0012g0069 a0001c0002t0012g0143 others(3): Show |
6 | HG01884.hp1 HG02109.hp2 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.400+77C>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145515090 | |||||||
| chr4:145515134 | C | CTG | 62 | a0001c0001t0001g0009 a0001c0001t0001g0056 a0001c0001t0001g0122 others(59): Show |
69 | HG00099.hp1 HG00408.hp1 HG00438.hp1 others(66): Show |
intron_variant | MODIFIER | c.400+163_400+164dup others(2): Show |
SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr4 | 145515134 | ||||||
| chr4:145515134 | C | CTGTG | 36 | a0001c0001t0001g0057 a0001c0001t0001g0060 a0001c0001t0001g0070 others(33): Show |
37 | HG00423.hp2 HG00438.hp2 HG00609.hp1 others(34): Show |
intron_variant | MODIFIER | c.400+161_400+164dup others(4): Show |
SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr4 | 145515134 | ||||||
| chr4:145515134 | C | CTGTGTG | 23 | a0001c0001t0001g0038 a0001c0001t0001g0101 a0001c0001t0001g0104 others(20): Show |
24 | HG01167.hp2 HG01169.hp1 HG01169.hp2 others(21): Show |
intron_variant | MODIFIER | c.400+159_400+164dup others(6): Show |
SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr4 | 145515134 | ||||||
| chr4:145515134 | C | CTGTGTGT others(1): Show |
6 | a0001c0001t0001g0225 a0001c0001t0003g0254 a0001c0001t0004g0061 others(3): Show |
6 | HG02735.hp1 HG02809.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.400+157_400+164dup others(8): Show |
SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr4 | 145515134 | ||||||
| chr4:145515134 | C | CTGTGTGT others(5): Show |
1 | a0001c0001t0020g0128 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.400+153_400+164dup others(12): Show |
SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr4 | 145515134 | ||||||
| chr4:145515134 | CTG | C | 52 | a0001c0001t0001g0003 a0001c0001t0001g0066 a0001c0001t0001g0067 others(49): Show |
62 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(59): Show |
intron_variant | MODIFIER | c.400+163_400+164del others(2): Show |
SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr4 | 145515134 | ||||||
| chr4:145515134 | CTGTG | C | 9 | a0001c0001t0001g0054 a0001c0001t0001g0078 a0001c0001t0001g0162 others(6): Show |
9 | HG01106.hp2 HG02109.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.400+161_400+164del others(4): Show |
SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr4 | 145515134 | ||||||
| chr4:145515134 | CTGTGTG | C | 4 | a0001c0001t0001g0203 a0001c0001t0002g0015 a0001c0001t0005g0044 others(1): Show |
5 | HG01981.hp2 HG02148.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.400+159_400+164del others(6): Show |
SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr4 | 145515134 | ||||||
| chr4:145515134 | CTGTGTGT others(1): Show |
C | 3 | a0001c0001t0007g0280 a0001c0001t0018g0077 a0001c0001t0018g0153 |
3 | HG02895.hp1 HG03540.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.400+157_400+164del others(8): Show |
SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr4 | 145515134 | ||||||
| chr4:145515134 | CTGTGTGT others(3): Show |
C | 4 | a0001c0001t0005g0048 a0001c0002t0012g0052 a0001c0002t0012g0069 others(1): Show |
4 | HG02132.hp1 HG02145.hp1 HG02257.hp2 others(1): Show |
intron_variant | MODIFIER | c.400+155_400+164del others(10): Show |
SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr4 | 145515134 | ||||||
| chr4:145515134 | CTGTGTGT others(5): Show |
C | 2 | a0001c0003t0012g0072 a0001c0003t0012g0144 |
2 | HG01884.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.400+153_400+164del others(12): Show |
SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr4 | 145515134 | ||||||
| chr4:145515134 | CTGTGTGT others(9): Show |
C | 1 | a0001c0001t0013g0042 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.400+149_400+164del others(16): Show |
SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr4 | 145515134 | ||||||
| chr4:145515147 | T | C | 3 | a0001c0001t0001g0157 a0001c0001t0001g0158 a0001c0001t0001g0159 |
3 | HG02135.hp1 NA18945.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.400+134T>C | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145515147 | |||||||
| chr4:145515170 | G | GTGTGTC | 3 | a0001c0001t0006g0215 a0001c0001t0006g0220 a0001c0001t0017g0216 |
3 | HG03654.hp1 NA18952.hp1 NA18974.hp1 |
intron_variant | MODIFIER | c.400+162_400+163ins others(6): Show |
SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr4 | 145515170 | ||||||
| chr4:145515170 | G | GTGTGTGT others(1): Show |
5 | a0001c0001t0006g0121 a0001c0001t0006g0217 a0001c0001t0006g0218 others(2): Show |
5 | HG01081.hp2 HG03927.hp1 HG03942.hp1 others(2): Show |
intron_variant | MODIFIER | c.400+164_400+171dup others(8): Show |
SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr4 | 145515170 | ||||||
| chr4:145515170 | G | GTGTGTGT others(3): Show |
2 | a0001c0001t0006g0213 a0001c0001t0017g0214 |
2 | HG00738.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.400+164_400+165ins others(10): Show |
SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr4 | 145515170 | ||||||
| chr4:145515174 | G | GTGTGTC | 3 | a0001c0001t0011g0073 a0001c0001t0011g0074 a0001c0001t0011g0145 |
3 | HG02647.hp2 HG03209.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.400+164_400+165ins others(6): Show |
SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr4 | 145515174 | ||||||
| chr4:145515199 | A | G | 94 | a0001c0001t0001g0009 a0001c0001t0001g0038 a0001c0001t0001g0054 others(91): Show |
101 | HG00423.hp2 HG00438.hp1 HG00621.hp1 others(98): Show |
intron_variant | MODIFIER | c.400+186A>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145515199 | |||||||
| chr4:145515208 | G | A | 1 | a0001c0001t0004g0079 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.400+195G>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145515208 | |||||||
| chr4:145515259 | G | A | 2 | a0001c0003t0012g0072 a0001c0003t0012g0144 |
2 | HG01884.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.400+246G>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145515259 | |||||||
| chr4:145515324 | T | G | 77 | a0001c0001t0001g0009 a0001c0001t0001g0038 a0001c0001t0001g0054 others(74): Show |
82 | HG00423.hp2 HG00438.hp1 HG00621.hp1 others(79): Show |
intron_variant | MODIFIER | c.400+311T>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145515324 | |||||||
| chr4:145515342 | T | C | 2 | a0001c0001t0001g0054 a0001c0001t0001g0078 |
2 | HG02109.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.400+329T>C | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145515342 | |||||||
| chr4:145515384 | A | C | 2 | a0001c0001t0001g0009 a0001c0001t0001g0038 |
3 | HG02622.hp1 HG03209.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.400+371A>C | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145515384 | |||||||
| chr4:145515446 | A | G | 6 | a0001c0002t0012g0052 a0001c0002t0012g0069 a0001c0002t0012g0143 others(3): Show |
6 | HG01884.hp1 HG02109.hp2 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.400+433A>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145515446 | |||||||
| chr4:145515457 | A | G | 1 | a0001c0001t0004g0105 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.400+444A>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145515457 | |||||||
| chr4:145515526 | C | T | 6 | a0001c0002t0012g0052 a0001c0002t0012g0069 a0001c0002t0012g0143 others(3): Show |
6 | HG01884.hp1 HG02109.hp2 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.400+513C>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145515526 | |||||||
| chr4:145515540 | G | A | 1 | a0001c0001t0027g0142 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.400+527G>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145515540 | |||||||
| chr4:145515561 | A | G | 2 | a0001c0003t0012g0072 a0001c0003t0012g0144 |
2 | HG01884.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.400+548A>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145515561 | |||||||
| chr4:145515664 | A | G | 6 | a0001c0002t0012g0052 a0001c0002t0012g0069 a0001c0002t0012g0143 others(3): Show |
6 | HG01884.hp1 HG02109.hp2 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.400+651A>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145515664 | |||||||
| chr4:145515782 | A | G | 3 | a0001c0002t0012g0052 a0001c0002t0012g0069 a0001c0002t0012g0143 |
3 | HG02145.hp1 HG02257.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.400+769A>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145515782 | |||||||
| chr4:145515867 | G | A | 3 | a0001c0002t0012g0052 a0001c0002t0012g0069 a0001c0002t0012g0143 |
3 | HG02145.hp1 HG02257.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.400+854G>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145515867 | |||||||
| chr4:145515967 | G | T | 1 | a0001c0001t0001g0269 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.400+954G>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145515967 | |||||||
| chr4:145516070 | C | G | 1 | a0001c0001t0004g0109 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.400+1057C>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145516070 | |||||||
| chr4:145516239 | T | C | 94 | a0001c0001t0001g0009 a0001c0001t0001g0038 a0001c0001t0001g0054 others(91): Show |
101 | HG00423.hp2 HG00438.hp1 HG00621.hp1 others(98): Show |
intron_variant | MODIFIER | c.400+1226T>C | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145516239 | |||||||
| chr4:145516315 | G | A | 1 | a0001c0001t0020g0236 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.400+1302G>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145516315 | |||||||
| chr4:145516346 | G | T | 9 | a0001c0001t0007g0280 a0001c0001t0008g0020 a0001c0001t0008g0053 others(6): Show |
11 | HG01192.hp2 HG01496.hp2 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.400+1333G>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145516346 | |||||||
| chr4:145516354 | T | C | 3 | a0001c0002t0012g0052 a0001c0002t0012g0069 a0001c0002t0012g0143 |
3 | HG02145.hp1 HG02257.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.400+1341T>C | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145516354 | |||||||
| chr4:145516487 | A | G | 1 | a0001c0001t0017g0216 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.400+1474A>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145516487 | |||||||
| chr4:145516489 | T | A | 94 | a0001c0001t0001g0009 a0001c0001t0001g0038 a0001c0001t0001g0054 others(91): Show |
101 | HG00423.hp2 HG00438.hp1 HG00621.hp1 others(98): Show |
intron_variant | MODIFIER | c.400+1476T>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145516489 | |||||||
| chr4:145516560 | C | T | 12 | a0001c0001t0006g0119 a0001c0001t0006g0120 a0001c0001t0006g0121 others(9): Show |
12 | HG00738.hp2 HG01081.hp2 HG03654.hp1 others(9): Show |
intron_variant | MODIFIER | c.400+1547C>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145516560 | |||||||
| chr4:145516629 | C | T | 5 | a0001c0001t0004g0055 a0001c0001t0004g0079 a0001c0001t0004g0080 others(2): Show |
5 | HG02572.hp2 HG02895.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.400+1616C>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145516629 | |||||||
| chr4:145516643 | T | C | 3 | a0001c0001t0002g0261 a0001c0001t0002g0263 a0001c0001t0002g0271 |
3 | NA18979.hp1 NA18984.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.400+1630T>C | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145516643 | |||||||
| chr4:145516664 | G | A | 4 | a0001c0001t0007g0280 a0001c0001t0015g0011 a0001c0001t0015g0161 others(1): Show |
5 | HG02055.hp2 HG02280.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.400+1651G>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145516664 | |||||||
| chr4:145516773 | A | C | 1 | a0002c0004t0002g0170 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.400+1760A>C | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145516773 | |||||||
| chr4:145516831 | A | G | 1 | a0001c0001t0001g0158 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.400+1818A>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145516831 | |||||||
| chr4:145517065 | C | G | 1 | a0001c0001t0002g0198 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.400+2052C>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145517065 | |||||||
| chr4:145517116 | C | T | 3 | a0001c0001t0002g0261 a0001c0001t0002g0263 a0001c0001t0002g0271 |
3 | NA18979.hp1 NA18984.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.400+2103C>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145517116 | |||||||
| chr4:145517129 | A | G | 8 | a0001c0001t0018g0077 a0001c0001t0018g0153 a0001c0002t0012g0052 others(5): Show |
8 | HG01884.hp1 HG02109.hp2 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.400+2116A>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145517129 | |||||||
| chr4:145517495 | T | A | 1 | a0001c0001t0002g0175 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.400+2482T>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145517495 | |||||||
| chr4:145517512 | G | A | 1 | a0001c0001t0004g0062 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.400+2499G>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145517512 | |||||||
| chr4:145517654 | TTTGGCCA others(1637): Show |
T | 54 | a0001c0001t0001g0243 a0001c0001t0003g0004 a0001c0001t0003g0016 others(51): Show |
59 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(56): Show |
intron_variant | MODIFIER | c.400+2649_400+4292d others(2): Show |
SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr4 | 145517654 | ||||||
| chr4:145517731 | A | G | 17 | a0001c0001t0004g0007 a0001c0001t0004g0061 a0001c0001t0004g0062 others(14): Show |
18 | HG00423.hp2 HG00621.hp1 HG01175.hp1 others(15): Show |
intron_variant | MODIFIER | c.400+2718A>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145517731 | |||||||
| chr4:145518222 | A | G | 6 | a0001c0002t0012g0052 a0001c0002t0012g0069 a0001c0002t0012g0143 others(3): Show |
6 | HG01884.hp1 HG02109.hp2 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.400+3209A>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145518222 | |||||||
| chr4:145518234 | A | G | 2 | a0001c0001t0018g0077 a0001c0001t0018g0153 |
2 | HG02895.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.400+3221A>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145518234 | |||||||
| chr4:145518243 | G | A | 1 | a0001c0001t0002g0209 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.400+3230G>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145518243 | |||||||
| chr4:145518279 | G | A | 4 | a0001c0001t0013g0040 a0001c0001t0013g0041 a0001c0001t0013g0042 others(1): Show |
4 | HG02735.hp1 HG03017.hp2 HG03490.hp2 others(1): Show |
intron_variant | MODIFIER | c.400+3266G>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145518279 | |||||||
| chr4:145518310 | A | G | 1 | a0001c0002t0030g0075 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.400+3297A>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145518310 | |||||||
| chr4:145518350 | G | A | 1 | a0001c0001t0001g0156 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.400+3337G>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145518350 | |||||||
| chr4:145518452 | G | T | 3 | a0001c0001t0001g0013 a0001c0001t0001g0103 a0001c0001t0001g0205 |
4 | HG02486.hp1 HG02622.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.400+3439G>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145518452 | |||||||
| chr4:145518500 | AAT | A | 6 | a0001c0001t0009g0035 a0001c0002t0012g0052 a0001c0002t0012g0069 others(3): Show |
6 | HG01884.hp1 HG02145.hp1 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.400+3489_400+3490d others(4): Show |
SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr4 | 145518500 | ||||||
| chr4:145518501 | AT | A | 81 | a0001c0001t0001g0054 a0001c0001t0001g0078 a0001c0001t0001g0094 others(78): Show |
86 | HG00423.hp2 HG00438.hp1 HG00621.hp1 others(83): Show |
intron_variant | MODIFIER | c.400+3489delT | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145518501 | |||||||
| chr4:145518502 | T | A | 26 | a0001c0001t0001g0043 a0001c0001t0001g0066 a0001c0001t0001g0067 others(23): Show |
28 | HG00738.hp2 HG01081.hp2 HG01192.hp2 others(25): Show |
intron_variant | MODIFIER | c.400+3489T>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145518502 | |||||||
| chr4:145518517 | T | G | 8 | a0001c0001t0018g0077 a0001c0001t0018g0153 a0001c0002t0012g0052 others(5): Show |
8 | HG01884.hp1 HG02109.hp2 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.400+3504T>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145518517 | |||||||
| chr4:145518555 | A | G | 1 | a0001c0001t0002g0199 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.400+3542A>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145518555 | |||||||
| chr4:145518567 | A | G | 76 | a0001c0001t0001g0054 a0001c0001t0001g0078 a0001c0001t0001g0094 others(73): Show |
80 | HG00423.hp2 HG00438.hp1 HG00621.hp1 others(77): Show |
intron_variant | MODIFIER | c.400+3554A>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145518567 | |||||||
| chr4:145518652 | A | C | 47 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0010 others(44): Show |
52 | HG00408.hp2 HG00423.hp1 HG00544.hp2 others(49): Show |
intron_variant | MODIFIER | c.400+3639A>C | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145518652 | |||||||
| chr4:145518748 | TCTG | T | 6 | a0001c0002t0012g0052 a0001c0002t0012g0069 a0001c0002t0012g0143 others(3): Show |
6 | HG01884.hp1 HG02109.hp2 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.400+3739_400+3741d others(5): Show |
SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr4 | 145518748 | ||||||
| chr4:145518829 | G | A | 2 | a0001c0003t0012g0072 a0001c0003t0012g0144 |
2 | HG01884.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.400+3816G>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145518829 | |||||||
| chr4:145518923 | A | G | 97 | a0001c0001t0001g0043 a0001c0001t0001g0054 a0001c0001t0001g0066 others(94): Show |
103 | HG00423.hp2 HG00438.hp1 HG00621.hp1 others(100): Show |
intron_variant | MODIFIER | c.400+3910A>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145518923 | |||||||
| chr4:145519088 | C | CT | 38 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0122 others(35): Show |
38 | HG00408.hp2 HG00423.hp2 HG00558.hp1 others(35): Show |
intron_variant | MODIFIER | c.400+4100dupT | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr4 | 145519088 | ||||||
| chr4:145519088 | C | CTT | 21 | a0001c0001t0001g0043 a0001c0001t0001g0067 a0001c0001t0002g0100 others(18): Show |
21 | HG00738.hp2 HG01081.hp2 HG02145.hp1 others(18): Show |
intron_variant | MODIFIER | c.400+4099_400+4100d others(4): Show |
SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr4 | 145519088 | ||||||
| chr4:145519088 | C | CTTT | 9 | a0001c0001t0001g0066 a0001c0001t0001g0071 a0001c0001t0002g0087 others(6): Show |
9 | HG00673.hp1 HG00673.hp2 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.400+4098_400+4100d others(5): Show |
SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr4 | 145519088 | ||||||
| chr4:145519088 | CT | C | 9 | a0001c0001t0001g0211 a0001c0001t0001g0268 a0001c0001t0002g0065 others(6): Show |
9 | HG01070.hp1 HG01167.hp1 HG01255.hp1 others(6): Show |
intron_variant | MODIFIER | c.400+4100delT | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr4 | 145519088 | ||||||
| chr4:145519127 | G | A | 3 | a0001c0001t0007g0280 a0001c0003t0012g0072 a0001c0003t0012g0144 |
3 | HG01884.hp1 HG02109.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.400+4114G>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145519127 | |||||||
| chr4:145519145 | G | A | 2 | a0001c0001t0001g0265 a0001c0001t0001g0272 |
2 | HG03704.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.400+4132G>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145519145 | |||||||
| chr4:145519240 | C | T | 1 | a0001c0001t0002g0091 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.400+4227C>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145519240 | |||||||
| chr4:145519305 | A | G | 3 | a0001c0002t0012g0052 a0001c0002t0012g0069 a0001c0002t0012g0143 |
3 | HG02145.hp1 HG02257.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.400+4292A>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145519305 | |||||||
| chr4:145519337 | C | G | 4 | a0001c0001t0001g0157 a0001c0001t0001g0158 a0001c0001t0001g0159 others(1): Show |
4 | HG02135.hp1 HG04228.hp1 NA18945.hp1 others(1): Show |
intron_variant | MODIFIER | c.400+4324C>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145519337 | |||||||
| chr4:145519396 | G | C | 54 | a0001c0001t0001g0243 a0001c0001t0003g0004 a0001c0001t0003g0016 others(51): Show |
59 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(56): Show |
intron_variant | MODIFIER | c.400+4383G>C | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145519396 | |||||||
| chr4:145519397 | AAC | A | 54 | a0001c0001t0001g0243 a0001c0001t0003g0004 a0001c0001t0003g0016 others(51): Show |
59 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(56): Show |
intron_variant | MODIFIER | c.400+4385_400+4386d others(4): Show |
SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145519397 | |||||||
| chr4:145519400 | C | G | 54 | a0001c0001t0001g0243 a0001c0001t0003g0004 a0001c0001t0003g0016 others(51): Show |
59 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(56): Show |
intron_variant | MODIFIER | c.400+4387C>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145519400 | |||||||
| chr4:145519402 | T | A | 54 | a0001c0001t0001g0243 a0001c0001t0003g0004 a0001c0001t0003g0016 others(51): Show |
59 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(56): Show |
intron_variant | MODIFIER | c.400+4389T>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145519402 | |||||||
| chr4:145519404 | T | G | 54 | a0001c0001t0001g0243 a0001c0001t0003g0004 a0001c0001t0003g0016 others(51): Show |
59 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(56): Show |
intron_variant | MODIFIER | c.400+4391T>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145519404 | |||||||
| chr4:145519405 | T | G | 54 | a0001c0001t0001g0243 a0001c0001t0003g0004 a0001c0001t0003g0016 others(51): Show |
59 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(56): Show |
intron_variant | MODIFIER | c.400+4392T>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145519405 | |||||||
| chr4:145519465 | G | A | 2 | a0001c0001t0018g0077 a0001c0001t0018g0153 |
2 | HG02895.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.400+4452G>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145519465 | |||||||
| chr4:145519489 | AT | A | 10 | a0001c0001t0001g0108 a0001c0001t0001g0203 a0001c0001t0001g0210 others(7): Show |
10 | HG01070.hp1 HG01071.hp1 HG01106.hp2 others(7): Show |
intron_variant | MODIFIER | c.400+4490delT | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr4 | 145519489 | ||||||
| chr4:145519644 | T | C | 99 | a0001c0001t0001g0009 a0001c0001t0001g0038 a0001c0001t0001g0043 others(96): Show |
106 | HG00423.hp2 HG00438.hp1 HG00621.hp1 others(103): Show |
intron_variant | MODIFIER | c.400+4631T>C | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145519644 | |||||||
| chr4:145519664 | A | AAAG | 10 | a0001c0001t0013g0040 a0001c0001t0013g0042 a0001c0001t0018g0077 others(7): Show |
10 | HG01884.hp1 HG02109.hp2 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.400+4653_400+4654i others(5): Show |
SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr4 | 145519664 | ||||||
| chr4:145519664 | A | AAG | 155 | a0001c0001t0001g0043 a0001c0001t0001g0054 a0001c0001t0001g0066 others(152): Show |
167 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(164): Show |
intron_variant | MODIFIER | c.400+4652_400+4653i others(4): Show |
SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr4 | 145519664 | ||||||
| chr4:145519846 | C | T | 78 | a0001c0001t0001g0054 a0001c0001t0001g0078 a0001c0001t0001g0094 others(75): Show |
82 | HG00423.hp2 HG00438.hp1 HG00621.hp1 others(79): Show |
intron_variant | MODIFIER | c.400+4833C>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145519846 | |||||||
| chr4:145519943 | G | T | 1 | a0001c0001t0011g0005 | 2 | HG02559.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.400+4930G>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145519943 | |||||||
| chr4:145520156 | A | C | 2 | a0001c0001t0003g0093 a0001c0001t0007g0092 |
2 | HG00609.hp2 HG02071.hp1 |
intron_variant | MODIFIER | c.400+5143A>C | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145520156 | |||||||
| chr4:145520288 | A | C | 1 | a0001c0001t0032g0277 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.400+5275A>C | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145520288 | |||||||
| chr4:145520578 | A | G | 1 | a0001c0001t0027g0142 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.400+5565A>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145520578 | |||||||
| chr4:145520727 | T | C | 2 | a0001c0001t0004g0136 a0001c0001t0004g0253 |
2 | NA18944.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.400+5714T>C | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145520727 | |||||||
| chr4:145520729 | A | C | 1 | a0001c0001t0001g0159 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.400+5716A>C | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145520729 | |||||||
| chr4:145520798 | C | T | 1 | a0001c0001t0004g0055 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.400+5785C>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145520798 | |||||||
| chr4:145520932 | A | G | 1 | a0001c0001t0001g0095 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.400+5919A>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145520932 | |||||||
| chr4:145521049 | G | A | 1 | a0001c0001t0003g0240 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.400+6036G>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145521049 | |||||||
| chr4:145521061 | A | G | 2 | a0001c0001t0018g0077 a0001c0001t0018g0153 |
2 | HG02895.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.400+6048A>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145521061 | |||||||
| chr4:145521101 | C | G | 1 | a0001c0001t0004g0151 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.400+6088C>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145521101 | |||||||
| chr4:145521193 | G | C | 3 | a0001c0001t0001g0101 a0001c0001t0004g0201 a0001c0001t0004g0202 |
3 | HG02717.hp1 HG02809.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.400+6180G>C | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145521193 | |||||||
| chr4:145521194 | G | A | 12 | a0001c0001t0006g0119 a0001c0001t0006g0120 a0001c0001t0006g0121 others(9): Show |
12 | HG00738.hp2 HG01081.hp2 HG03654.hp1 others(9): Show |
intron_variant | MODIFIER | c.400+6181G>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145521194 | |||||||
| chr4:145521238 | A | G | 1 | a0001c0001t0002g0176 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.400+6225A>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145521238 | |||||||
| chr4:145521510 | C | T | 1 | a0001c0001t0001g0259 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.400+6497C>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145521510 | |||||||
| chr4:145521731 | C | T | 2 | a0001c0001t0018g0077 a0001c0001t0018g0153 |
2 | HG02895.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.400+6718C>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145521731 | |||||||
| chr4:145521828 | G | A | 4 | a0001c0001t0001g0043 a0001c0001t0001g0066 a0001c0001t0001g0067 others(1): Show |
4 | HG02145.hp2 HG02451.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.400+6815G>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145521828 | |||||||
| chr4:145521900 | T | TA | 15 | a0001c0001t0001g0003 a0001c0001t0001g0095 a0001c0001t0001g0156 others(12): Show |
18 | HG01175.hp2 HG01433.hp2 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.400+6905dupA | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr4 | 145521900 | ||||||
| chr4:145521900 | TA | T | 69 | a0001c0001t0001g0043 a0001c0001t0001g0054 a0001c0001t0001g0078 others(66): Show |
72 | HG00423.hp2 HG00621.hp1 HG01081.hp1 others(69): Show |
intron_variant | MODIFIER | c.400+6905delA | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr4 | 145521900 | ||||||
| chr4:145521900 | TAA | T | 7 | a0001c0001t0004g0014 a0001c0001t0005g0025 a0001c0001t0005g0045 others(4): Show |
8 | HG00438.hp1 HG02135.hp2 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.400+6904_400+6905d others(4): Show |
SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr4 | 145521900 | ||||||
| chr4:145521946 | C | G | 1 | a0001c0001t0001g0043 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.400+6933C>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145521946 | |||||||
| chr4:145522094 | T | TGAGGAGA others(4): Show |
8 | a0001c0001t0018g0077 a0001c0001t0018g0153 a0001c0002t0012g0052 others(5): Show |
8 | HG01884.hp1 HG02109.hp2 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.400+7083_400+7084i others(13): Show |
SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr4 | 145522094 | ||||||
| chr4:145522117 | A | G | 4 | a0001c0001t0001g0043 a0001c0001t0001g0066 a0001c0001t0001g0067 others(1): Show |
4 | HG02145.hp2 HG02451.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.400+7104A>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145522117 | |||||||
| chr4:145522248 | G | A | 2 | a0001c0003t0012g0072 a0001c0003t0012g0144 |
2 | HG01884.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.400+7235G>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145522248 | |||||||
| chr4:145522253 | C | T | 2 | a0001c0001t0006g0121 a0001c0001t0006g0220 |
2 | NA18973.hp1 NA18974.hp1 |
intron_variant | MODIFIER | c.400+7240C>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145522253 | |||||||
| chr4:145522298 | C | CA | 12 | a0001c0001t0006g0119 a0001c0001t0006g0120 a0001c0001t0006g0121 others(9): Show |
12 | HG00738.hp2 HG01081.hp2 HG03654.hp1 others(9): Show |
intron_variant | MODIFIER | c.400+7292dupA | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr4 | 145522298 | ||||||
| chr4:145522319 | G | C | 3 | a0001c0002t0012g0052 a0001c0002t0012g0069 a0001c0002t0012g0143 |
3 | HG02145.hp1 HG02257.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.400+7306G>C | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145522319 | |||||||
| chr4:145522361 | G | A | 4 | a0001c0001t0007g0280 a0001c0001t0015g0011 a0001c0001t0015g0161 others(1): Show |
5 | HG02055.hp2 HG02280.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.400+7348G>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145522361 | |||||||
| chr4:145522366 | C | T | 2 | a0001c0001t0018g0077 a0001c0001t0018g0153 |
2 | HG02895.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.400+7353C>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145522366 | |||||||
| chr4:145522374 | G | A | 4 | a0001c0001t0011g0005 a0001c0001t0011g0073 a0001c0001t0011g0074 others(1): Show |
5 | HG02559.hp1 HG02647.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.400+7361G>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145522374 | |||||||
| chr4:145522464 | G | A | 1 | a0001c0001t0002g0166 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.400+7451G>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145522464 | |||||||
| chr4:145522573 | T | C | 1 | a0001c0001t0004g0117 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.400+7560T>C | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145522573 | |||||||
| chr4:145522654 | GTGTTT | G | 5 | a0001c0001t0008g0020 a0001c0001t0008g0053 a0001c0001t0008g0155 others(2): Show |
6 | HG01192.hp2 HG01496.hp2 HG01891.hp2 others(3): Show |
intron_variant | MODIFIER | c.400+7663_400+7667d others(7): Show |
SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr4 | 145522654 | ||||||
| chr4:145522684 | G | GT | 6 | a0001c0001t0003g0252 a0001c0001t0009g0006 a0001c0001t0009g0023 others(3): Show |
7 | HG01175.hp2 HG01261.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.400+7679dupT | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr4 | 145522684 | ||||||
| chr4:145522886 | C | T | 3 | a0001c0002t0012g0052 a0001c0002t0012g0069 a0001c0002t0012g0143 |
3 | HG02145.hp1 HG02257.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.400+7873C>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145522886 | |||||||
| chr4:145522924 | G | A | 3 | a0001c0001t0001g0060 a0001c0001t0001g0102 a0001c0001t0001g0204 |
3 | HG02451.hp2 HG03579.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.400+7911G>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145522924 | |||||||
| chr4:145522957 | G | A | 3 | a0001c0002t0012g0052 a0001c0002t0012g0069 a0001c0002t0012g0143 |
3 | HG02145.hp1 HG02257.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.400+7944G>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145522957 | |||||||
| chr4:145523214 | T | C | 6 | a0001c0002t0012g0052 a0001c0002t0012g0069 a0001c0002t0012g0143 others(3): Show |
6 | HG01884.hp1 HG02109.hp2 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.400+8201T>C | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145523214 | |||||||
| chr4:145523279 | G | A | 1 | a0001c0002t0030g0075 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.400+8266G>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145523279 | |||||||
| chr4:145523285 | A | G | 4 | a0001c0001t0001g0157 a0001c0001t0001g0158 a0001c0001t0001g0159 others(1): Show |
4 | HG02135.hp1 HG04228.hp1 NA18945.hp1 others(1): Show |
intron_variant | MODIFIER | c.400+8272A>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145523285 | |||||||
| chr4:145523440 | A | G | 1 | a0001c0001t0004g0080 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.400+8427A>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145523440 | |||||||
| chr4:145523483 | A | G | 2 | a0001c0001t0010g0132 a0001c0001t0010g0245 |
2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.400+8470A>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145523483 | |||||||
| chr4:145523492 | T | G | 5 | a0001c0001t0008g0020 a0001c0001t0008g0053 a0001c0001t0008g0155 others(2): Show |
6 | HG01192.hp2 HG01496.hp2 HG01891.hp2 others(3): Show |
intron_variant | MODIFIER | c.400+8479T>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145523492 | |||||||
| chr4:145523636 | G | A | 2 | a0001c0001t0001g0265 a0001c0001t0001g0272 |
2 | HG03704.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.400+8623G>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145523636 | |||||||
| chr4:145523732 | G | A | 2 | a0001c0001t0001g0264 a0001c0001t0001g0266 |
2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.400+8719G>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145523732 | |||||||
| chr4:145523863 | T | C | 1 | a0001c0001t0003g0249 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.400+8850T>C | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145523863 | |||||||
| chr4:145524067 | GA | G | 3 | a0001c0002t0012g0052 a0001c0002t0012g0069 a0001c0002t0012g0143 |
3 | HG02145.hp1 HG02257.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.400+9056delA | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr4 | 145524067 | ||||||
| chr4:145524131 | A | G | 1 | a0001c0002t0030g0075 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.400+9118A>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145524131 | |||||||
| chr4:145524143 | C | G | 3 | a0001c0002t0012g0052 a0001c0002t0012g0069 a0001c0002t0012g0143 |
3 | HG02145.hp1 HG02257.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.400+9130C>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145524143 | |||||||
| chr4:145524372 | T | C | 3 | a0001c0002t0012g0052 a0001c0002t0012g0069 a0001c0002t0012g0143 |
3 | HG02145.hp1 HG02257.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.400+9359T>C | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145524372 | |||||||
| chr4:145524405 | T | A | 3 | a0001c0001t0001g0054 a0001c0001t0001g0078 a0001c0001t0001g0162 |
3 | HG02109.hp1 HG02258.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.400+9392T>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145524405 | |||||||
| chr4:145524528 | T | C | 168 | a0001c0001t0001g0009 a0001c0001t0001g0038 a0001c0001t0001g0043 others(165): Show |
181 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(178): Show |
intron_variant | MODIFIER | c.400+9515T>C | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145524528 | |||||||
| chr4:145524718 | T | A | 4 | a0001c0001t0001g0043 a0001c0001t0001g0066 a0001c0001t0001g0067 others(1): Show |
4 | HG02145.hp2 HG02451.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.400+9705T>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145524718 | |||||||
| chr4:145524738 | G | A | 1 | a0001c0001t0026g0037 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.400+9725G>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145524738 | |||||||
| chr4:145524790 | GA | G | 278 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0013 others(275): Show |
305 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(302): Show |
intron_variant | MODIFIER | c.400+9790delA | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr4 | 145524790 | ||||||
| chr4:145525236 | A | G | 3 | a0001c0002t0012g0052 a0001c0002t0012g0069 a0001c0002t0012g0143 |
3 | HG02145.hp1 HG02257.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.400+10223A>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145525236 | |||||||
| chr4:145525269 | G | A | 8 | a0001c0001t0018g0077 a0001c0001t0018g0153 a0001c0002t0012g0052 others(5): Show |
8 | HG01884.hp1 HG02109.hp2 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.400+10256G>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145525269 | |||||||
| chr4:145525289 | A | G | 2 | a0001c0001t0001g0009 a0001c0001t0001g0038 |
3 | HG02622.hp1 HG03209.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.400+10276A>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145525289 | |||||||
| chr4:145525820 | G | A | 1 | a0001c0002t0030g0075 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.400+10807G>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145525820 | |||||||
| chr4:145525952 | T | C | 1 | a0001c0002t0030g0075 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.400+10939T>C | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145525952 | |||||||
| chr4:145526041 | T | C | 103 | a0001c0001t0001g0009 a0001c0001t0001g0038 a0001c0001t0001g0043 others(100): Show |
111 | HG00423.hp2 HG00438.hp1 HG00621.hp1 others(108): Show |
intron_variant | MODIFIER | c.400+11028T>C | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145526041 | |||||||
| chr4:145526077 | A | T | 1 | a0001c0001t0001g0205 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.400+11064A>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145526077 | |||||||
| chr4:145526450 | A | G | 1 | a0001c0001t0001g0043 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.400+11437A>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145526450 | |||||||
| chr4:145526563 | AGGACCCA others(1344): Show |
A | 5 | a0001c0001t0005g0024 a0001c0001t0005g0025 a0001c0001t0005g0045 others(2): Show |
5 | HG00438.hp1 HG02135.hp2 NA18964.hp2 others(2): Show |
intron_variant | MODIFIER | c.400+11551_401-1189 others(4): Show |
SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145526563 | |||||||
| chr4:145526608 | A | G | 3 | a0001c0001t0002g0261 a0001c0001t0002g0263 a0001c0001t0002g0271 |
3 | NA18979.hp1 NA18984.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.400+11595A>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145526608 | |||||||
| chr4:145526637 | T | C | 84 | a0001c0001t0001g0054 a0001c0001t0001g0078 a0001c0001t0001g0094 others(81): Show |
90 | HG00423.hp2 HG00621.hp1 HG01081.hp1 others(87): Show |
intron_variant | MODIFIER | c.400+11624T>C | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145526637 | |||||||
| chr4:145526856 | A | C | 2 | a0001c0001t0002g0002 a0001c0001t0002g0088 |
2 | HG00558.hp1 HG00597.hp1 |
intron_variant | MODIFIER | c.400+11843A>C | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145526856 | |||||||
| chr4:145526872 | C | T | 84 | a0001c0001t0001g0054 a0001c0001t0001g0078 a0001c0001t0001g0094 others(81): Show |
90 | HG00423.hp2 HG00621.hp1 HG01081.hp1 others(87): Show |
intron_variant | MODIFIER | c.400+11859C>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145526872 | |||||||
| chr4:145527227 | CT | C | 83 | a0001c0001t0001g0054 a0001c0001t0001g0078 a0001c0001t0001g0094 others(80): Show |
89 | HG00423.hp2 HG00621.hp1 HG01081.hp1 others(86): Show |
intron_variant | MODIFIER | c.400+12228delT | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr4 | 145527227 | ||||||
| chr4:145527254 | T | C | 90 | a0001c0001t0001g0009 a0001c0001t0001g0038 a0001c0001t0001g0043 others(87): Show |
97 | HG00423.hp2 HG00621.hp1 HG01081.hp1 others(94): Show |
intron_variant | MODIFIER | c.400+12241T>C | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145527254 | |||||||
| chr4:145527283 | G | A | 2 | a0001c0001t0003g0135 a0001c0001t0003g0252 |
2 | HG01175.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.400+12270G>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145527283 | |||||||
| chr4:145527292 | C | T | 4 | a0001c0001t0001g0043 a0001c0001t0001g0066 a0001c0001t0001g0067 others(1): Show |
4 | HG02145.hp2 HG02451.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.400+12279C>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145527292 | |||||||
| chr4:145527368 | C | T | 2 | a0001c0001t0002g0097 a0001c0001t0002g0193 |
2 | NA19002.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.400+12355C>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145527368 | |||||||
| chr4:145527425 | G | A | 9 | a0001c0001t0001g0094 a0001c0001t0001g0138 a0001c0001t0001g0139 others(6): Show |
10 | HG01081.hp1 HG01257.hp2 HG01928.hp2 others(7): Show |
intron_variant | MODIFIER | c.401-12379G>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145527425 | |||||||
| chr4:145527671 | C | T | 4 | a0001c0001t0007g0280 a0001c0001t0015g0011 a0001c0001t0015g0161 others(1): Show |
5 | HG02055.hp2 HG02280.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.401-12133C>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145527671 | |||||||
| chr4:145527767 | T | A | 11 | a0001c0001t0005g0026 a0001c0001t0005g0027 a0001c0001t0005g0028 others(8): Show |
11 | HG01243.hp2 HG01884.hp2 HG02040.hp1 others(8): Show |
intron_variant | MODIFIER | c.401-12037T>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145527767 | |||||||
| chr4:145527863 | AT | A | 50 | a0001c0001t0001g0043 a0001c0001t0001g0054 a0001c0001t0001g0078 others(47): Show |
53 | HG00423.hp2 HG00621.hp1 HG01081.hp1 others(50): Show |
intron_variant | MODIFIER | c.401-11927delT | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr4 | 145527863 | ||||||
| chr4:145527916 | A | T | 5 | a0001c0001t0005g0024 a0001c0001t0005g0025 a0001c0001t0005g0045 others(2): Show |
5 | HG00438.hp1 HG02135.hp2 NA18964.hp2 others(2): Show |
intron_variant | MODIFIER | c.401-11888A>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145527916 | |||||||
| chr4:145527917 | G | GA | 5 | a0001c0001t0005g0024 a0001c0001t0005g0025 a0001c0001t0005g0045 others(2): Show |
5 | HG00438.hp1 HG02135.hp2 NA18964.hp2 others(2): Show |
intron_variant | MODIFIER | c.401-11887_401-1188 others(5): Show |
SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145527917 | |||||||
| chr4:145527962 | G | A | 1 | a0001c0001t0001g0225 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.401-11842G>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145527962 | |||||||
| chr4:145528060 | T | TAC | 22 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0187 others(19): Show |
24 | HG00735.hp1 HG00738.hp2 HG01081.hp2 others(21): Show |
intron_variant | MODIFIER | c.401-11712_401-1171 others(6): Show |
SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr4 | 145528060 | ||||||
| chr4:145528060 | T | TACAC | 4 | a0001c0001t0002g0086 a0001c0001t0006g0217 a0001c0001t0017g0214 others(1): Show |
4 | HG00140.hp2 HG04204.hp1 NA18952.hp1 others(1): Show |
intron_variant | MODIFIER | c.401-11714_401-1171 others(8): Show |
SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr4 | 145528060 | ||||||
| chr4:145528060 | TAC | T | 6 | a0001c0001t0018g0077 a0001c0001t0018g0153 a0001c0002t0012g0052 others(3): Show |
6 | HG02145.hp1 HG02257.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.401-11712_401-1171 others(6): Show |
SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr4 | 145528060 | ||||||
| chr4:145528060 | TACAC | T | 9 | a0001c0001t0001g0033 a0001c0001t0001g0146 a0001c0001t0004g0079 others(6): Show |
10 | HG02572.hp2 HG02965.hp2 HG02976.hp2 others(7): Show |
intron_variant | MODIFIER | c.401-11714_401-1171 others(8): Show |
SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr4 | 145528060 | ||||||
| chr4:145528060 | TACACAC | T | 49 | a0001c0001t0001g0054 a0001c0001t0001g0078 a0001c0001t0001g0094 others(46): Show |
53 | HG00423.hp2 HG00621.hp1 HG01081.hp1 others(50): Show |
intron_variant | MODIFIER | c.401-11716_401-1171 others(10): Show |
SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr4 | 145528060 | ||||||
| chr4:145528060 | TACACACA others(1): Show |
T | 24 | a0001c0001t0004g0149 a0001c0001t0004g0150 a0001c0001t0004g0151 others(21): Show |
26 | HG00438.hp2 HG01243.hp1 HG01243.hp2 others(23): Show |
intron_variant | MODIFIER | c.401-11718_401-1171 others(12): Show |
SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr4 | 145528060 | ||||||
| chr4:145528060 | TACACACA others(5): Show |
T | 1 | a0001c0001t0009g0023 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.401-11722_401-1171 others(16): Show |
SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr4 | 145528060 | ||||||
| chr4:145528084 | CACACACA others(3): Show |
C | 7 | a0001c0001t0005g0024 a0001c0001t0005g0025 a0001c0001t0005g0039 others(4): Show |
7 | HG00438.hp1 HG02135.hp2 NA18964.hp2 others(4): Show |
intron_variant | MODIFIER | c.401-11708_401-1169 others(14): Show |
SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr4 | 145528084 | ||||||
| chr4:145528094 | T | C | 1 | a0001c0001t0005g0048 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.401-11710T>C | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145528094 | |||||||
| chr4:145528107 | AT | A | 6 | a0001c0001t0001g0211 a0001c0001t0002g0164 a0001c0001t0004g0014 others(3): Show |
6 | HG01069.hp2 HG01070.hp1 HG01884.hp1 others(3): Show |
intron_variant | MODIFIER | c.401-11683delT | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr4 | 145528107 | ||||||
| chr4:145528122 | G | T | 29 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0056 others(26): Show |
31 | HG00140.hp1 HG00544.hp1 HG00609.hp2 others(28): Show |
intron_variant | MODIFIER | c.401-11682G>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145528122 | |||||||
| chr4:145528249 | G | A | 3 | a0001c0001t0002g0090 a0001c0001t0002g0171 a0001c0001t0002g0191 |
3 | HG00544.hp2 NA18747.hp1 NA18747.hp2 |
intron_variant | MODIFIER | c.401-11555G>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145528249 | |||||||
| chr4:145528304 | T | C | 1 | a0001c0001t0008g0155 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.401-11500T>C | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145528304 | |||||||
| chr4:145528394 | C | T | 4 | a0001c0001t0011g0005 a0001c0001t0011g0073 a0001c0001t0011g0074 others(1): Show |
5 | HG02559.hp1 HG02647.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.401-11410C>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145528394 | |||||||
| chr4:145528428 | C | CG | 27 | a0001c0001t0004g0149 a0001c0001t0004g0150 a0001c0001t0004g0151 others(24): Show |
28 | HG00438.hp1 HG01243.hp1 HG01243.hp2 others(25): Show |
intron_variant | MODIFIER | c.401-11370dupG | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr4 | 145528428 | ||||||
| chr4:145528949 | G | A | 2 | a0001c0001t0018g0077 a0001c0001t0018g0153 |
2 | HG02895.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.401-10855G>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145528949 | |||||||
| chr4:145529305 | G | A | 1 | a0001c0001t0001g0162 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.401-10499G>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145529305 | |||||||
| chr4:145529753 | T | C | 3 | a0001c0001t0001g0022 a0001c0001t0001g0264 a0001c0001t0001g0266 |
4 | HG01516.hp1 HG01517.hp2 HG01928.hp1 others(1): Show |
intron_variant | MODIFIER | c.401-10051T>C | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145529753 | |||||||
| chr4:145529818 | G | A | 51 | a0001c0001t0003g0004 a0001c0001t0003g0016 a0001c0001t0003g0018 others(48): Show |
56 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(53): Show |
intron_variant | MODIFIER | c.401-9986G>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145529818 | |||||||
| chr4:145529829 | A | G | 2 | a0001c0003t0012g0072 a0001c0003t0012g0144 |
2 | HG01884.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.401-9975A>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145529829 | |||||||
| chr4:145529875 | G | A | 2 | a0001c0001t0010g0132 a0001c0001t0010g0245 |
2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.401-9929G>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145529875 | |||||||
| chr4:145529895 | T | A | 1 | a0001c0001t0001g0183 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.401-9909T>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145529895 | |||||||
| chr4:145529907 | T | C | 1 | a0001c0001t0011g0005 | 2 | HG02559.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.401-9897T>C | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145529907 | |||||||
| chr4:145529979 | A | C | 2 | a0001c0001t0008g0031 a0001c0001t0008g0032 |
2 | HG02976.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.401-9825A>C | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145529979 | |||||||
| chr4:145530075 | G | A | 4 | a0001c0001t0004g0007 a0001c0001t0004g0110 a0001c0001t0004g0111 others(1): Show |
5 | HG00423.hp2 HG02132.hp2 NA18945.hp2 others(2): Show |
intron_variant | MODIFIER | c.401-9729G>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145530075 | |||||||
| chr4:145530604 | A | C | 95 | a0001c0001t0001g0009 a0001c0001t0001g0038 a0001c0001t0001g0043 others(92): Show |
102 | HG00423.hp2 HG00438.hp1 HG00621.hp1 others(99): Show |
intron_variant | MODIFIER | c.401-9200A>C | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145530604 | |||||||
| chr4:145530628 | C | A | 91 | a0001c0001t0001g0009 a0001c0001t0001g0038 a0001c0001t0001g0054 others(88): Show |
98 | HG00423.hp2 HG00438.hp1 HG00621.hp1 others(95): Show |
intron_variant | MODIFIER | c.401-9176C>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145530628 | |||||||
| chr4:145530705 | A | AAAACTAT others(315): Show |
2 | a0001c0003t0012g0072 a0001c0003t0012g0144 |
2 | HG01884.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.401-9082_401-9081i others(324): Show |
SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr4 | 145530705 | ||||||
| chr4:145531056 | C | T | 1 | a0001c0001t0007g0280 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.401-8748C>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145531056 | |||||||
| chr4:145531245 | G | A | 1 | a0001c0002t0012g0052 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.401-8559G>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145531245 | |||||||
| chr4:145531364 | C | T | 1 | a0001c0001t0002g0176 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.401-8440C>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145531364 | |||||||
| chr4:145531399 | C | G | 1 | a0001c0001t0009g0023 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.401-8405C>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145531399 | |||||||
| chr4:145531621 | T | C | 87 | a0001c0001t0001g0009 a0001c0001t0001g0038 a0001c0001t0001g0054 others(84): Show |
94 | HG00423.hp2 HG00438.hp1 HG00621.hp1 others(91): Show |
intron_variant | MODIFIER | c.401-8183T>C | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145531621 | |||||||
| chr4:145531715 | A | C | 1 | a0001c0002t0012g0069 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.401-8089A>C | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145531715 | |||||||
| chr4:145531958 | G | A | 27 | a0001c0001t0004g0149 a0001c0001t0004g0150 a0001c0001t0004g0151 others(24): Show |
28 | HG00438.hp1 HG01243.hp1 HG01243.hp2 others(25): Show |
intron_variant | MODIFIER | c.401-7846G>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145531958 | |||||||
| chr4:145532147 | A | G | 3 | a0001c0001t0002g0096 a0001c0001t0002g0178 a0001c0001t0002g0189 |
3 | HG00099.hp2 HG01099.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.401-7657A>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145532147 | |||||||
| chr4:145532274 | C | T | 27 | a0001c0001t0004g0149 a0001c0001t0004g0150 a0001c0001t0004g0151 others(24): Show |
28 | HG00438.hp1 HG01243.hp1 HG01243.hp2 others(25): Show |
intron_variant | MODIFIER | c.401-7530C>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145532274 | |||||||
| chr4:145532428 | G | A | 1 | a0001c0001t0026g0037 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.401-7376G>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145532428 | |||||||
| chr4:145532428 | G | GT | 4 | a0001c0001t0001g0108 a0001c0001t0001g0210 a0001c0001t0001g0211 others(1): Show |
4 | HG01070.hp1 HG01071.hp1 HG01106.hp2 others(1): Show |
intron_variant | MODIFIER | c.401-7370dupT | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr4 | 145532428 | ||||||
| chr4:145532503 | A | T | 1 | a0001c0001t0001g0157 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.401-7301A>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145532503 | |||||||
| chr4:145532521 | T | C | 1 | a0001c0001t0001g0182 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.401-7283T>C | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145532521 | |||||||
| chr4:145532731 | C | T | 16 | a0001c0001t0005g0024 a0001c0001t0005g0025 a0001c0001t0005g0026 others(13): Show |
16 | HG00438.hp1 HG01243.hp2 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.401-7073C>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145532731 | |||||||
| chr4:145532769 | G | A | 44 | a0001c0001t0001g0054 a0001c0001t0001g0078 a0001c0001t0001g0094 others(41): Show |
47 | HG00423.hp2 HG00621.hp1 HG01081.hp1 others(44): Show |
intron_variant | MODIFIER | c.401-7035G>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145532769 | |||||||
| chr4:145532775 | T | C | 1 | a0001c0002t0030g0075 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.401-7029T>C | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145532775 | |||||||
| chr4:145532777 | G | C | 4 | a0001c0001t0001g0043 a0001c0001t0001g0066 a0001c0001t0001g0067 others(1): Show |
4 | HG02145.hp2 HG02451.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.401-7027G>C | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145532777 | |||||||
| chr4:145532963 | T | A | 1 | a0001c0001t0001g0188 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.401-6841T>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145532963 | |||||||
| chr4:145533196 | AG | A | 13 | a0001c0001t0006g0119 a0001c0001t0006g0120 a0001c0001t0006g0121 others(10): Show |
13 | HG00738.hp2 HG01081.hp2 HG03654.hp1 others(10): Show |
intron_variant | MODIFIER | c.401-6605delG | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr4 | 145533196 | ||||||
| chr4:145533253 | G | A | 1 | a0001c0001t0006g0213 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.401-6551G>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145533253 | |||||||
| chr4:145533293 | G | C | 2 | a0001c0001t0019g0059 a0001c0001t0019g0212 |
2 | HG02723.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.401-6511G>C | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145533293 | |||||||
| chr4:145533477 | G | C | 2 | a0001c0001t0018g0077 a0001c0001t0018g0153 |
2 | HG02895.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.401-6327G>C | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145533477 | |||||||
| chr4:145533535 | T | C | 49 | a0001c0001t0003g0004 a0001c0001t0003g0016 a0001c0001t0003g0018 others(46): Show |
53 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(50): Show |
intron_variant | MODIFIER | c.401-6269T>C | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145533535 | |||||||
| chr4:145533598 | C | T | 4 | a0001c0001t0011g0005 a0001c0001t0011g0073 a0001c0001t0011g0074 others(1): Show |
5 | HG02559.hp1 HG02647.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.401-6206C>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145533598 | |||||||
| chr4:145533928 | C | T | 2 | a0001c0001t0018g0077 a0001c0001t0018g0153 |
2 | HG02895.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.401-5876C>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145533928 | |||||||
| chr4:145534377 | G | A | 1 | a0001c0001t0002g0086 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.401-5427G>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145534377 | |||||||
| chr4:145534505 | C | G | 3 | a0001c0001t0015g0011 a0001c0001t0015g0161 a0001c0001t0027g0142 |
4 | HG02055.hp2 HG02280.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.401-5299C>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145534505 | |||||||
| chr4:145534513 | T | A | 1 | a0001c0001t0001g0104 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.401-5291T>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145534513 | |||||||
| chr4:145534660 | C | T | 2 | a0001c0003t0012g0072 a0001c0003t0012g0144 |
2 | HG01884.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.401-5144C>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145534660 | |||||||
| chr4:145534684 | T | C | 5 | a0001c0001t0001g0122 a0001c0001t0001g0223 a0001c0001t0001g0224 others(2): Show |
6 | HG01891.hp1 HG02895.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.401-5120T>C | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145534684 | |||||||
| chr4:145534866 | G | A | 1 | a0001c0001t0007g0092 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.401-4938G>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145534866 | |||||||
| chr4:145535037 | A | G | 169 | a0001c0001t0001g0009 a0001c0001t0001g0038 a0001c0001t0001g0043 others(166): Show |
182 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(179): Show |
intron_variant | MODIFIER | c.401-4767A>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145535037 | |||||||
| chr4:145535392 | C | T | 1 | a0001c0001t0002g0209 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.401-4412C>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145535392 | |||||||
| chr4:145535536 | G | C | 1 | a0001c0001t0027g0142 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.401-4268G>C | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145535536 | |||||||
| chr4:145535600 | G | A | 1 | a0001c0003t0012g0072 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.401-4204G>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145535600 | |||||||
| chr4:145535832 | C | T | 3 | a0001c0001t0001g0058 a0001c0001t0003g0093 a0001c0001t0007g0092 |
3 | HG00609.hp2 HG02040.hp2 HG02071.hp1 |
intron_variant | MODIFIER | c.401-3972C>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145535832 | |||||||
| chr4:145535967 | C | G | 2 | a0001c0001t0006g0119 a0001c0001t0006g0120 |
2 | NA18975.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.401-3837C>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145535967 | |||||||
| chr4:145535984 | C | CA | 11 | a0001c0001t0003g0135 a0001c0001t0003g0244 a0001c0001t0003g0252 others(8): Show |
12 | HG01167.hp2 HG01169.hp2 HG01175.hp2 others(9): Show |
intron_variant | MODIFIER | c.401-3804dupA | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr4 | 145535984 | ||||||
| chr4:145536149 | G | A | 1 | a0001c0001t0023g0208 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.401-3655G>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145536149 | |||||||
| chr4:145536226 | T | C | 5 | a0001c0001t0008g0020 a0001c0001t0008g0053 a0001c0001t0008g0155 others(2): Show |
6 | HG01192.hp2 HG01496.hp2 HG01891.hp2 others(3): Show |
intron_variant | MODIFIER | c.401-3578T>C | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145536226 | |||||||
| chr4:145536234 | C | T | 4 | a0001c0001t0007g0280 a0001c0001t0015g0011 a0001c0001t0015g0161 others(1): Show |
5 | HG02055.hp2 HG02280.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.401-3570C>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145536234 | |||||||
| chr4:145536246 | G | C | 2 | a0001c0001t0003g0129 a0001c0001t0003g0238 |
2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.401-3558G>C | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145536246 | |||||||
| chr4:145536259 | A | G | 1 | a0001c0001t0002g0100 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.401-3545A>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145536259 | |||||||
| chr4:145536530 | C | A | 1 | a0001c0001t0001g0173 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.401-3274C>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145536530 | |||||||
| chr4:145537032 | G | A | 1 | a0001c0001t0002g0099 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.401-2772G>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145537032 | |||||||
| chr4:145537393 | G | C | 1 | a0001c0001t0004g0116 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.401-2411G>C | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145537393 | |||||||
| chr4:145537570 | G | T | 2 | a0001c0001t0018g0077 a0001c0001t0018g0153 |
2 | HG02895.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.401-2234G>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145537570 | |||||||
| chr4:145537643 | T | C | 1 | a0001c0001t0004g0055 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.401-2161T>C | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145537643 | |||||||
| chr4:145537962 | G | A | 1 | a0001c0001t0001g0043 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.401-1842G>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145537962 | |||||||
| chr4:145537962 | G | T | 13 | a0001c0001t0005g0027 a0001c0001t0005g0028 a0001c0001t0005g0029 others(10): Show |
14 | HG01192.hp2 HG01496.hp2 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.401-1842G>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145537962 | |||||||
| chr4:145538023 | G | A | 2 | a0001c0001t0001g0057 a0001c0001t0001g0095 |
2 | NA18941.hp2 NA18995.hp2 |
intron_variant | MODIFIER | c.401-1781G>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145538023 | |||||||
| chr4:145538072 | A | G | 2 | a0001c0001t0018g0077 a0001c0001t0018g0153 |
2 | HG02895.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.401-1732A>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145538072 | |||||||
| chr4:145538107 | C | T | 1 | a0001c0001t0002g0194 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.401-1697C>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145538107 | |||||||
| chr4:145538136 | T | C | 51 | a0001c0001t0001g0043 a0001c0001t0001g0066 a0001c0001t0001g0067 others(48): Show |
55 | HG00438.hp1 HG01192.hp2 HG01243.hp1 others(52): Show |
intron_variant | MODIFIER | c.401-1668T>C | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145538136 | |||||||
| chr4:145538747 | G | T | 23 | a0001c0001t0005g0024 a0001c0001t0005g0025 a0001c0001t0005g0026 others(20): Show |
24 | HG00438.hp1 HG01243.hp2 HG01261.hp1 others(21): Show |
intron_variant | MODIFIER | c.401-1057G>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145538747 | |||||||
| chr4:145538901 | C | T | 38 | a0001c0001t0005g0024 a0001c0001t0005g0025 a0001c0001t0005g0026 others(35): Show |
41 | HG00438.hp1 HG01192.hp2 HG01243.hp2 others(38): Show |
intron_variant | MODIFIER | c.401-903C>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145538901 | |||||||
| chr4:145539057 | C | T | 7 | a0001c0001t0008g0020 a0001c0001t0008g0053 a0001c0001t0008g0155 others(4): Show |
8 | HG01070.hp2 HG01192.hp2 HG01433.hp1 others(5): Show |
intron_variant | MODIFIER | c.401-747C>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145539057 | |||||||
| chr4:145539188 | G | A | 2 | a0001c0001t0018g0077 a0001c0001t0018g0153 |
2 | HG02895.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.401-616G>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145539188 | |||||||
| chr4:145539403 | C | T | 28 | a0001c0001t0001g0094 a0001c0001t0001g0138 a0001c0001t0001g0139 others(25): Show |
30 | HG00423.hp2 HG00621.hp1 HG01081.hp1 others(27): Show |
intron_variant | MODIFIER | c.401-401C>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145539403 | |||||||
| chr4:145539488 | T | G | 1 | a0001c0001t0001g0173 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.401-316T>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145539488 | |||||||
| chr4:145540197 | G | A | 1 | a0001c0001t0023g0208 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.658+136G>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 3/6 | chr4 | 145540197 | |||||||
| chr4:145540284 | A | G | 2 | a0001c0001t0003g0134 a0001c0001t0003g0250 |
2 | HG01516.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.658+223A>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 3/6 | chr4 | 145540284 | |||||||
| chr4:145540382 | C | T | 88 | a0001c0001t0001g0094 a0001c0001t0001g0122 a0001c0001t0001g0138 others(85): Show |
94 | HG00423.hp2 HG00438.hp1 HG00621.hp1 others(91): Show |
intron_variant | MODIFIER | c.658+321C>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 3/6 | chr4 | 145540382 | |||||||
| chr4:145540462 | G | A | 1 | a0001c0001t0004g0105 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.658+401G>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 3/6 | chr4 | 145540462 | |||||||
| chr4:145540538 | C | T | 1 | a0001c0001t0001g0146 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.658+477C>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 3/6 | chr4 | 145540538 | |||||||
| chr4:145540548 | G | A | 2 | a0001c0001t0018g0077 a0001c0001t0018g0153 |
2 | HG02895.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.658+487G>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 3/6 | chr4 | 145540548 | |||||||
| chr4:145540627 | A | G | 1 | a0001c0001t0007g0280 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.658+566A>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 3/6 | chr4 | 145540627 | |||||||
| chr4:145540900 | A | T | 1 | a0001c0001t0001g0033 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.658+839A>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 3/6 | chr4 | 145540900 | |||||||
| chr4:145541339 | T | TAGTATCA others(184): Show |
1 | a0001c0001t0008g0256 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.659-1180_659-1179i others(193): Show |
SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr4 | 145541339 | ||||||
| chr4:145541403 | C | T | 5 | a0001c0001t0008g0020 a0001c0001t0008g0053 a0001c0001t0008g0155 others(2): Show |
6 | HG01192.hp2 HG01496.hp2 HG01891.hp2 others(3): Show |
intron_variant | MODIFIER | c.659-1179C>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 3/6 | chr4 | 145541403 | |||||||
| chr4:145541481 | C | A | 1 | a0001c0001t0001g0183 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.659-1101C>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 3/6 | chr4 | 145541481 | |||||||
| chr4:145541481 | C | T | 1 | a0001c0001t0001g0160 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.659-1101C>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 3/6 | chr4 | 145541481 | |||||||
| chr4:145541482 | G | A | 1 | a0001c0001t0004g0149 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.659-1100G>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 3/6 | chr4 | 145541482 | |||||||
| chr4:145541728 | T | G | 3 | a0001c0001t0015g0011 a0001c0001t0015g0161 a0001c0001t0027g0142 |
4 | HG02055.hp2 HG02280.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.659-854T>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 3/6 | chr4 | 145541728 | |||||||
| chr4:145541787 | T | C | 2 | a0001c0001t0003g0131 a0001c0001t0003g0276 |
2 | HG00639.hp2 HG01993.hp2 |
intron_variant | MODIFIER | c.659-795T>C | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 3/6 | chr4 | 145541787 | |||||||
| chr4:145541993 | T | C | 122 | a0001c0001t0001g0009 a0001c0001t0001g0038 a0001c0001t0001g0094 others(119): Show |
132 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(129): Show |
intron_variant | MODIFIER | c.659-589T>C | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 3/6 | chr4 | 145541993 | |||||||
| chr4:145542118 | T | C | 2 | a0001c0001t0009g0034 a0001c0001t0009g0154 |
2 | HG01261.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.659-464T>C | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 3/6 | chr4 | 145542118 | |||||||
| chr4:145542285 | A | G | 1 | a0001c0001t0001g0043 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.659-297A>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 3/6 | chr4 | 145542285 | |||||||
| chr4:145542293 | G | T | 1 | a0001c0001t0004g0202 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.659-289G>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 3/6 | chr4 | 145542293 | |||||||
| chr4:145542374 | A | C | 4 | a0001c0001t0001g0043 a0001c0001t0001g0066 a0001c0001t0001g0067 others(1): Show |
4 | HG02145.hp2 HG02451.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.659-208A>C | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 3/6 | chr4 | 145542374 | |||||||
| chr4:145542398 | T | C | 16 | a0001c0001t0005g0024 a0001c0001t0005g0025 a0001c0001t0005g0026 others(13): Show |
16 | HG00438.hp1 HG01243.hp2 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.659-184T>C | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 3/6 | chr4 | 145542398 | |||||||
| chr4:145542552 | T | C | 1 | a0001c0001t0023g0208 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.659-30T>C | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 3/6 | chr4 | 145542552 | |||||||
| chr4:145542814 | T | C | 167 | a0001c0001t0001g0009 a0001c0001t0001g0038 a0001c0001t0001g0043 others(164): Show |
180 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(177): Show |
intron_variant | MODIFIER | c.775+116T>C | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 4/6 | chr4 | 145542814 | |||||||
| chr4:145542851 | A | G | 2 | a0001c0001t0018g0077 a0001c0001t0018g0153 |
2 | HG02895.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.775+153A>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 4/6 | chr4 | 145542851 | |||||||
| chr4:145543127 | C | T | 2 | a0001c0003t0012g0072 a0001c0003t0012g0144 |
2 | HG01884.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.775+429C>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 4/6 | chr4 | 145543127 | |||||||
| chr4:145543274 | G | T | 1 | a0001c0001t0007g0280 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.775+576G>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 4/6 | chr4 | 145543274 | |||||||
| chr4:145543321 | G | A | 1 | a0001c0001t0005g0049 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.775+623G>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 4/6 | chr4 | 145543321 | |||||||
| chr4:145543353 | A | G | 4 | a0001c0001t0001g0043 a0001c0001t0001g0066 a0001c0001t0001g0067 others(1): Show |
4 | HG02145.hp2 HG02451.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.775+655A>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 4/6 | chr4 | 145543353 | |||||||
| chr4:145543545 | C | CAGCCTGA others(8): Show |
1 | a0001c0001t0002g0167 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.775+848_775+862dup others(15): Show |
SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr4 | 145543545 | ||||||
| chr4:145543576 | A | C | 3 | a0001c0001t0005g0027 a0001c0001t0005g0028 a0001c0001t0005g0047 |
3 | HG01884.hp2 HG03130.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.775+878A>C | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 4/6 | chr4 | 145543576 | |||||||
| chr4:145543621 | C | T | 73 | a0001c0001t0003g0004 a0001c0001t0003g0016 a0001c0001t0003g0018 others(70): Show |
79 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(76): Show |
intron_variant | MODIFIER | c.775+923C>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 4/6 | chr4 | 145543621 | |||||||
| chr4:145543928 | C | T | 2 | a0001c0001t0019g0059 a0001c0001t0019g0212 |
2 | HG02723.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.775+1230C>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 4/6 | chr4 | 145543928 | |||||||
| chr4:145543942 | T | C | 83 | a0001c0001t0001g0009 a0001c0001t0001g0038 a0001c0001t0001g0094 others(80): Show |
90 | HG00423.hp2 HG00438.hp1 HG00621.hp1 others(87): Show |
intron_variant | MODIFIER | c.775+1244T>C | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 4/6 | chr4 | 145543942 | |||||||
| chr4:145544191 | AG | A | 3 | a0001c0002t0012g0052 a0001c0002t0012g0069 a0001c0002t0012g0143 |
3 | HG02145.hp1 HG02257.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.775+1495delG | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr4 | 145544191 | ||||||
| chr4:145544195 | A | G | 1 | a0001c0001t0002g0167 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.775+1497A>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 4/6 | chr4 | 145544195 | |||||||
| chr4:145544197 | G | C | 1 | a0001c0001t0002g0167 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.775+1499G>C | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 4/6 | chr4 | 145544197 | |||||||
| chr4:145544213 | C | T | 2 | a0001c0001t0010g0132 a0001c0001t0010g0245 |
2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.775+1515C>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 4/6 | chr4 | 145544213 | |||||||
| chr4:145544227 | CTCTG | C | 4 | a0001c0001t0001g0043 a0001c0001t0001g0066 a0001c0001t0001g0067 others(1): Show |
4 | HG02145.hp2 HG02451.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.775+1533_775+1536d others(6): Show |
SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr4 | 145544227 | ||||||
| chr4:145544253 | G | A | 2 | a0001c0001t0018g0077 a0001c0001t0018g0153 |
2 | HG02895.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.775+1555G>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 4/6 | chr4 | 145544253 | |||||||
| chr4:145544287 | C | T | 88 | a0001c0001t0001g0094 a0001c0001t0001g0122 a0001c0001t0001g0138 others(85): Show |
94 | HG00423.hp2 HG00438.hp1 HG00621.hp1 others(91): Show |
intron_variant | MODIFIER | c.775+1589C>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 4/6 | chr4 | 145544287 | |||||||
| chr4:145544458 | G | T | 1 | a0001c0001t0002g0167 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.775+1760G>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 4/6 | chr4 | 145544458 | |||||||
| chr4:145544581 | C | CA | 5 | a0001c0001t0009g0006 a0001c0001t0009g0034 a0001c0001t0009g0035 others(2): Show |
6 | HG01261.hp1 HG02630.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.775+1895dupA | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr4 | 145544581 | ||||||
| chr4:145544661 | A | G | 1 | a0001c0001t0004g0106 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.775+1963A>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 4/6 | chr4 | 145544661 | |||||||
| chr4:145544924 | G | A | 1 | a0001c0001t0002g0167 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.776-1779G>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 4/6 | chr4 | 145544924 | |||||||
| chr4:145544925 | A | G | 1 | a0001c0001t0002g0167 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.776-1778A>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 4/6 | chr4 | 145544925 | |||||||
| chr4:145545082 | G | A | 3 | a0001c0001t0015g0011 a0001c0001t0015g0161 a0001c0001t0027g0142 |
4 | HG02055.hp2 HG02280.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.776-1621G>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 4/6 | chr4 | 145545082 | |||||||
| chr4:145545217 | G | A | 4 | a0001c0001t0001g0108 a0001c0001t0001g0203 a0001c0001t0001g0210 others(1): Show |
4 | HG01070.hp1 HG01071.hp1 HG01106.hp2 others(1): Show |
intron_variant | MODIFIER | c.776-1486G>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 4/6 | chr4 | 145545217 | |||||||
| chr4:145545220 | A | C | 1 | a0001c0001t0001g0070 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.776-1483A>C | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 4/6 | chr4 | 145545220 | |||||||
| chr4:145545274 | C | G | 1 | a0001c0001t0004g0062 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.776-1429C>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 4/6 | chr4 | 145545274 | |||||||
| chr4:145545311 | T | C | 1 | a0001c0001t0002g0195 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.776-1392T>C | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 4/6 | chr4 | 145545311 | |||||||
| chr4:145545313 | G | A | 1 | a0001c0001t0002g0195 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.776-1390G>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 4/6 | chr4 | 145545313 | |||||||
| chr4:145545453 | T | A | 2 | a0001c0003t0012g0072 a0001c0003t0012g0144 |
2 | HG01884.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.776-1250T>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 4/6 | chr4 | 145545453 | |||||||
| chr4:145545521 | T | C | 5 | a0001c0001t0009g0006 a0001c0001t0009g0034 a0001c0001t0009g0035 others(2): Show |
6 | HG01261.hp1 HG02630.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.776-1182T>C | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 4/6 | chr4 | 145545521 | |||||||
| chr4:145545537 | A | G | 1 | a0001c0001t0002g0171 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.776-1166A>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 4/6 | chr4 | 145545537 | |||||||
| chr4:145545549 | G | GT | 154 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0021 others(151): Show |
171 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(168): Show |
intron_variant | MODIFIER | c.776-1144dupT | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr4 | 145545549 | ||||||
| chr4:145545549 | G | GTT | 7 | a0001c0001t0001g0009 a0001c0001t0001g0038 a0001c0001t0004g0105 others(4): Show |
9 | HG02055.hp2 HG02280.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.776-1145_776-1144d others(4): Show |
SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr4 | 145545549 | ||||||
| chr4:145545556 | T | G | 4 | a0001c0001t0003g0241 a0001c0001t0018g0077 a0001c0001t0018g0153 others(1): Show |
4 | HG01070.hp2 HG02602.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.776-1147T>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 4/6 | chr4 | 145545556 | |||||||
| chr4:145545556 | T | TG | 8 | a0001c0001t0005g0026 a0001c0001t0005g0027 a0001c0001t0007g0280 others(5): Show |
9 | HG01192.hp2 HG01243.hp2 HG01496.hp2 others(6): Show |
intron_variant | MODIFIER | c.776-1147_776-1146i others(3): Show |
SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 4/6 | chr4 | 145545556 | |||||||
| chr4:145545556 | T | TGTG | 13 | a0001c0001t0005g0024 a0001c0001t0005g0025 a0001c0001t0005g0029 others(10): Show |
13 | HG00438.hp1 HG02040.hp1 HG02132.hp1 others(10): Show |
intron_variant | MODIFIER | c.776-1147_776-1146i others(5): Show |
SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 4/6 | chr4 | 145545556 | |||||||
| chr4:145545556 | T | TTG | 45 | a0001c0001t0003g0004 a0001c0001t0003g0016 a0001c0001t0003g0018 others(42): Show |
50 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(47): Show |
intron_variant | MODIFIER | c.776-1146_776-1145i others(4): Show |
SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr4 | 145545556 | ||||||
| chr4:145545556 | T | TTGTG | 12 | a0001c0001t0006g0119 a0001c0001t0006g0120 a0001c0001t0006g0121 others(9): Show |
12 | HG00738.hp2 HG01081.hp2 HG03927.hp1 others(9): Show |
intron_variant | MODIFIER | c.776-1146_776-1145i others(6): Show |
SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr4 | 145545556 | ||||||
| chr4:145545558 | T | G | 84 | a0001c0001t0003g0004 a0001c0001t0003g0016 a0001c0001t0003g0018 others(81): Show |
90 | HG00099.hp1 HG00408.hp1 HG00438.hp1 others(87): Show |
intron_variant | MODIFIER | c.776-1145T>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 4/6 | chr4 | 145545558 | |||||||
| chr4:145545558 | T | TG | 11 | a0001c0001t0001g0043 a0001c0001t0001g0066 a0001c0001t0001g0067 others(8): Show |
11 | HG00140.hp1 HG01884.hp2 HG01993.hp1 others(8): Show |
intron_variant | MODIFIER | c.776-1145_776-1144i others(3): Show |
SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 4/6 | chr4 | 145545558 | |||||||
| chr4:145545558 | T | TGTG | 10 | a0001c0001t0008g0031 a0001c0001t0008g0032 a0001c0001t0009g0006 others(7): Show |
11 | HG01261.hp1 HG01884.hp1 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.776-1145_776-1144i others(5): Show |
SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 4/6 | chr4 | 145545558 | |||||||
| chr4:145545558 | T | TTG | 10 | a0001c0001t0003g0234 a0001c0001t0003g0248 a0001c0001t0007g0251 others(7): Show |
11 | HG00609.hp1 HG02145.hp1 HG02148.hp2 others(8): Show |
intron_variant | MODIFIER | c.776-1125_776-1124d others(4): Show |
SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr4 | 145545558 | ||||||
| chr4:145545560 | G | T | 52 | a0001c0001t0001g0094 a0001c0001t0001g0104 a0001c0001t0001g0122 others(49): Show |
55 | HG00423.hp2 HG00621.hp1 HG01081.hp1 others(52): Show |
intron_variant | MODIFIER | c.776-1143G>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 4/6 | chr4 | 145545560 | |||||||
| chr4:145545625 | A | C | 13 | a0001c0001t0006g0119 a0001c0001t0006g0120 a0001c0001t0006g0121 others(10): Show |
13 | HG00738.hp2 HG01081.hp2 HG03654.hp1 others(10): Show |
intron_variant | MODIFIER | c.776-1078A>C | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 4/6 | chr4 | 145545625 | |||||||
| chr4:145545723 | C | T | 88 | a0001c0001t0001g0094 a0001c0001t0001g0122 a0001c0001t0001g0138 others(85): Show |
94 | HG00423.hp2 HG00438.hp1 HG00621.hp1 others(91): Show |
intron_variant | MODIFIER | c.776-980C>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 4/6 | chr4 | 145545723 | |||||||
| chr4:145545976 | G | T | 1 | a0001c0001t0002g0167 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.776-727G>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 4/6 | chr4 | 145545976 | |||||||
| chr4:145546046 | G | A | 2 | a0001c0001t0001g0101 a0001c0001t0001g0200 |
2 | HG02809.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.776-657G>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 4/6 | chr4 | 145546046 | |||||||
| chr4:145546274 | A | G | 88 | a0001c0001t0001g0094 a0001c0001t0001g0122 a0001c0001t0001g0138 others(85): Show |
94 | HG00423.hp2 HG00438.hp1 HG00621.hp1 others(91): Show |
intron_variant | MODIFIER | c.776-429A>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 4/6 | chr4 | 145546274 | |||||||
| chr4:145547179 | G | C | 4 | a0001c0001t0008g0031 a0001c0001t0008g0032 a0001c0001t0018g0077 others(1): Show |
4 | HG02895.hp1 HG02976.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.997+255G>C | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 5/6 | chr4 | 145547179 | |||||||
| chr4:145547291 | CAGTAAAT | C | 83 | a0001c0001t0001g0094 a0001c0001t0001g0122 a0001c0001t0001g0138 others(80): Show |
89 | HG00423.hp2 HG00438.hp1 HG00621.hp1 others(86): Show |
intron_variant | MODIFIER | c.997+370_997+376del others(7): Show |
SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr4 | 145547291 | ||||||
| chr4:145547469 | A | G | 1 | a0001c0001t0011g0074 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.997+545A>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 5/6 | chr4 | 145547469 | |||||||
| chr4:145547741 | G | C | 7 | a0001c0001t0005g0044 a0001c0001t0009g0006 a0001c0001t0009g0023 others(4): Show |
8 | HG01261.hp1 HG02630.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.997+817G>C | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 5/6 | chr4 | 145547741 | |||||||
| chr4:145547783 | T | C | 1 | a0001c0001t0020g0128 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.997+859T>C | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 5/6 | chr4 | 145547783 | |||||||
| chr4:145547888 | G | A | 3 | a0001c0001t0015g0011 a0001c0001t0015g0161 a0001c0001t0027g0142 |
4 | HG02055.hp2 HG02280.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.997+964G>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 5/6 | chr4 | 145547888 | |||||||
| chr4:145547896 | T | G | 1 | a0001c0001t0005g0047 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.997+972T>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 5/6 | chr4 | 145547896 | |||||||
| chr4:145547901 | C | CT | 73 | a0001c0001t0003g0004 a0001c0001t0003g0016 a0001c0001t0003g0018 others(70): Show |
79 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(76): Show |
intron_variant | MODIFIER | c.997+978dupT | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr4 | 145547901 | ||||||
| chr4:145547940 | T | A | 1 | a0001c0002t0030g0075 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.997+1016T>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 5/6 | chr4 | 145547940 | |||||||
| chr4:145548129 | T | A | 3 | a0001c0001t0001g0183 a0001c0001t0001g0184 a0001c0001t0001g0267 |
3 | HG02027.hp1 HG02155.hp1 NA18982.hp1 |
intron_variant | MODIFIER | c.997+1205T>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 5/6 | chr4 | 145548129 | |||||||
| chr4:145548202 | TTTTA | T | 4 | a0001c0001t0008g0031 a0001c0001t0008g0032 a0001c0001t0018g0077 others(1): Show |
4 | HG02895.hp1 HG02976.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.997+1304_997+1307d others(6): Show |
SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr4 | 145548202 | ||||||
| chr4:145548705 | A | G | 8 | a0001c0001t0013g0040 a0001c0001t0013g0041 a0001c0001t0013g0042 others(5): Show |
8 | HG02735.hp1 HG03017.hp2 HG03453.hp1 others(5): Show |
intron_variant | MODIFIER | c.997+1781A>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 5/6 | chr4 | 145548705 | |||||||
| chr4:145548786 | G | A | 165 | a0001c0001t0001g0043 a0001c0001t0001g0066 a0001c0001t0001g0067 others(162): Show |
177 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(174): Show |
intron_variant | MODIFIER | c.997+1862G>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 5/6 | chr4 | 145548786 | |||||||
| chr4:145548834 | G | A | 2 | a0001c0001t0018g0077 a0001c0001t0018g0153 |
2 | HG02895.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.997+1910G>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 5/6 | chr4 | 145548834 | |||||||
| chr4:145548890 | A | T | 1 | a0001c0001t0002g0169 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.997+1966A>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 5/6 | chr4 | 145548890 | |||||||
| chr4:145548907 | C | G | 1 | a0001c0001t0002g0181 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.997+1983C>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 5/6 | chr4 | 145548907 | |||||||
| chr4:145549047 | AC | A | 5 | a0001c0001t0008g0020 a0001c0001t0008g0053 a0001c0001t0008g0155 others(2): Show |
6 | HG01192.hp2 HG01496.hp2 HG01891.hp2 others(3): Show |
intron_variant | MODIFIER | c.997+2124delC | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 5/6 | chr4 | 145549047 | |||||||
| chr4:145549150 | A | G | 1 | a0001c0001t0001g0204 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.997+2226A>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 5/6 | chr4 | 145549150 | |||||||
| chr4:145549312 | T | C | 4 | a0001c0001t0001g0043 a0001c0001t0001g0066 a0001c0001t0001g0067 others(1): Show |
4 | HG02145.hp2 HG02451.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.997+2388T>C | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 5/6 | chr4 | 145549312 | |||||||
| chr4:145549433 | G | A | 4 | a0001c0001t0001g0122 a0001c0001t0001g0223 a0001c0001t0001g0224 others(1): Show |
4 | HG01891.hp1 HG03041.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.997+2509G>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 5/6 | chr4 | 145549433 | |||||||
| chr4:145549458 | GAC | G | 3 | a0001c0001t0001g0013 a0001c0001t0001g0103 a0001c0001t0001g0205 |
4 | HG02486.hp1 HG02622.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.997+2542_997+2543d others(4): Show |
SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr4 | 145549458 | ||||||
| chr4:145549867 | A | G | 1 | a0001c0001t0002g0180 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.997+2943A>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 5/6 | chr4 | 145549867 | |||||||
| chr4:145550089 | CTTAGT | C | 4 | a0001c0001t0014g0076 a0001c0001t0014g0147 a0001c0001t0014g0148 others(1): Show |
4 | HG03453.hp1 HG03471.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.997+3166_997+3170d others(7): Show |
SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 5/6 | chr4 | 145550089 | |||||||
| chr4:145550159 | A | G | 2 | a0001c0001t0008g0031 a0001c0001t0008g0032 |
2 | HG02976.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.997+3235A>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 5/6 | chr4 | 145550159 | |||||||
| chr4:145550283 | C | T | 2 | a0001c0001t0008g0031 a0001c0001t0008g0032 |
2 | HG02976.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.997+3359C>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 5/6 | chr4 | 145550283 | |||||||
| chr4:145550597 | A | G | 1 | a0001c0001t0001g0225 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.998-3187A>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 5/6 | chr4 | 145550597 | |||||||
| chr4:145550785 | T | C | 13 | a0001c0001t0006g0119 a0001c0001t0006g0120 a0001c0001t0006g0121 others(10): Show |
13 | HG00738.hp2 HG01081.hp2 HG03654.hp1 others(10): Show |
intron_variant | MODIFIER | c.998-2999T>C | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 5/6 | chr4 | 145550785 | |||||||
| chr4:145550889 | T | C | 23 | a0001c0001t0005g0024 a0001c0001t0005g0025 a0001c0001t0005g0026 others(20): Show |
24 | HG00438.hp1 HG01243.hp2 HG01261.hp1 others(21): Show |
intron_variant | MODIFIER | c.998-2895T>C | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 5/6 | chr4 | 145550889 | |||||||
| chr4:145550967 | T | G | 1 | a0001c0001t0001g0174 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.998-2817T>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 5/6 | chr4 | 145550967 | |||||||
| chr4:145551240 | C | T | 1 | a0001c0001t0005g0030 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.998-2544C>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 5/6 | chr4 | 145551240 | |||||||
| chr4:145551330 | A | G | 1 | a0001c0001t0001g0269 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.998-2454A>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 5/6 | chr4 | 145551330 | |||||||
| chr4:145551526 | G | C | 1 | a0001c0001t0002g0015 | 2 | HG01981.hp2 HG02148.hp1 |
intron_variant | MODIFIER | c.998-2258G>C | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 5/6 | chr4 | 145551526 | |||||||
| chr4:145551684 | A | G | 6 | a0001c0001t0009g0006 a0001c0001t0009g0023 a0001c0001t0009g0034 others(3): Show |
7 | HG01261.hp1 HG02630.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.998-2100A>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 5/6 | chr4 | 145551684 | |||||||
| chr4:145551738 | T | C | 1 | a0001c0001t0002g0086 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.998-2046T>C | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 5/6 | chr4 | 145551738 | |||||||
| chr4:145551997 | A | G | 1 | a0001c0001t0016g0246 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.998-1787A>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 5/6 | chr4 | 145551997 | |||||||
| chr4:145552184 | T | C | 1 | a0001c0001t0002g0177 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.998-1600T>C | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 5/6 | chr4 | 145552184 | |||||||
| chr4:145552189 | T | G | 1 | a0001c0001t0002g0177 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.998-1595T>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 5/6 | chr4 | 145552189 | |||||||
| chr4:145552297 | G | A | 26 | a0001c0001t0005g0024 a0001c0001t0005g0025 a0001c0001t0005g0026 others(23): Show |
28 | HG00438.hp1 HG01243.hp2 HG01261.hp1 others(25): Show |
intron_variant | MODIFIER | c.998-1487G>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 5/6 | chr4 | 145552297 | |||||||
| chr4:145552302 | G | A | 1 | a0001c0001t0001g0104 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.998-1482G>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 5/6 | chr4 | 145552302 | |||||||
| chr4:145552502 | T | C | 23 | a0001c0001t0005g0024 a0001c0001t0005g0025 a0001c0001t0005g0026 others(20): Show |
24 | HG00438.hp1 HG01243.hp2 HG01261.hp1 others(21): Show |
intron_variant | MODIFIER | c.998-1282T>C | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 5/6 | chr4 | 145552502 | |||||||
| chr4:145552512 | G | T | 1 | a0001c0001t0009g0154 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.998-1272G>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 5/6 | chr4 | 145552512 | |||||||
| chr4:145552583 | G | A | 1 | a0001c0001t0004g0279 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.998-1201G>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 5/6 | chr4 | 145552583 | |||||||
| chr4:145552605 | C | A | 1 | a0001c0001t0003g0231 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.998-1179C>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 5/6 | chr4 | 145552605 | |||||||
| chr4:145552669 | G | A | 1 | a0001c0001t0003g0134 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.998-1115G>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 5/6 | chr4 | 145552669 | |||||||
| chr4:145552798 | C | A | 1 | a0001c0001t0029g0113 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.998-986C>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 5/6 | chr4 | 145552798 | |||||||
| chr4:145552843 | A | G | 90 | a0001c0001t0001g0094 a0001c0001t0001g0122 a0001c0001t0001g0138 others(87): Show |
96 | HG00423.hp2 HG00438.hp1 HG00621.hp1 others(93): Show |
intron_variant | MODIFIER | c.998-941A>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 5/6 | chr4 | 145552843 | |||||||
| chr4:145552866 | A | G | 2 | a0001c0001t0002g0099 a0001c0001t0002g0197 |
2 | NA18944.hp2 NA18956.hp2 |
intron_variant | MODIFIER | c.998-918A>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 5/6 | chr4 | 145552866 | |||||||
| chr4:145552890 | A | G | 57 | a0001c0001t0003g0004 a0001c0001t0003g0016 a0001c0001t0003g0018 others(54): Show |
63 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(60): Show |
intron_variant | MODIFIER | c.998-894A>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 5/6 | chr4 | 145552890 | |||||||
| chr4:145552892 | ATGT | A | 84 | a0001c0001t0001g0094 a0001c0001t0001g0122 a0001c0001t0001g0138 others(81): Show |
90 | HG00423.hp2 HG00438.hp1 HG00621.hp1 others(87): Show |
intron_variant | MODIFIER | c.998-866_998-864del others(3): Show |
SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr4 | 145552892 | ||||||
| chr4:145553079 | A | AT | 144 | a0001c0001t0001g0043 a0001c0001t0001g0066 a0001c0001t0001g0067 others(141): Show |
156 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(153): Show |
intron_variant | MODIFIER | c.998-690dupT | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr4 | 145553079 | ||||||
| chr4:145553079 | A | ATT | 19 | a0001c0001t0005g0024 a0001c0001t0005g0025 a0001c0001t0005g0026 others(16): Show |
19 | HG00438.hp1 HG01243.hp2 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.998-691_998-690dup others(2): Show |
SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr4 | 145553079 | ||||||
| chr4:145553093 | T | G | 2 | a0001c0001t0007g0280 a0001c0001t0016g0275 |
2 | HG01169.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.998-691T>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 5/6 | chr4 | 145553093 | |||||||
| chr4:145553093 | T | TG | 3 | a0001c0001t0010g0132 a0001c0001t0010g0245 a0001c0001t0014g0147 |
3 | HG01167.hp2 HG01169.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.998-691_998-690ins others(1): Show |
SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 5/6 | chr4 | 145553093 | |||||||
| chr4:145553097 | G | A | 2 | a0001c0001t0008g0031 a0001c0001t0008g0032 |
2 | HG02976.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.998-687G>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 5/6 | chr4 | 145553097 | |||||||
| chr4:145553114 | G | A | 13 | a0001c0001t0006g0119 a0001c0001t0006g0120 a0001c0001t0006g0121 others(10): Show |
13 | HG00738.hp2 HG01081.hp2 HG03654.hp1 others(10): Show |
intron_variant | MODIFIER | c.998-670G>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 5/6 | chr4 | 145553114 | |||||||
| chr4:145553150 | A | G | 5 | a0001c0001t0008g0020 a0001c0001t0008g0053 a0001c0001t0008g0155 others(2): Show |
6 | HG01192.hp2 HG01496.hp2 HG01891.hp2 others(3): Show |
intron_variant | MODIFIER | c.998-634A>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 5/6 | chr4 | 145553150 | |||||||
| chr4:145553281 | G | A | 1 | a0001c0001t0003g0231 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.998-503G>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 5/6 | chr4 | 145553281 | |||||||
| chr4:145553292 | AT | A | 165 | a0001c0001t0001g0043 a0001c0001t0001g0066 a0001c0001t0001g0067 others(162): Show |
177 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(174): Show |
intron_variant | MODIFIER | c.998-487delT | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr4 | 145553292 | ||||||
| chr4:145553449 | G | A | 1 | a0001c0001t0008g0031 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.998-335G>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 5/6 | chr4 | 145553449 | |||||||
| chr4:145553452 | A | G | 1 | a0001c0001t0001g0022 | 2 | HG01928.hp1 HG02293.hp2 |
intron_variant | MODIFIER | c.998-332A>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 5/6 | chr4 | 145553452 | |||||||
| chr4:145553652 | C | T | 1 | a0001c0001t0013g0041 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.998-132C>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 5/6 | chr4 | 145553652 | |||||||
| chr4:145553690 | C | A | 2 | a0001c0001t0015g0011 a0001c0001t0015g0161 |
3 | HG02055.hp2 HG02280.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.998-94C>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 5/6 | chr4 | 145553690 | |||||||
| chr4:145553690 | C | T | 23 | a0001c0001t0005g0024 a0001c0001t0005g0025 a0001c0001t0005g0026 others(20): Show |
24 | HG00438.hp1 HG01243.hp2 HG01261.hp1 others(21): Show |
intron_variant | MODIFIER | c.998-94C>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 5/6 | chr4 | 145553690 | |||||||
| chr4:145554091 | C | CT | 7 | a0001c0001t0001g0146 a0001c0001t0002g0084 a0001c0001t0002g0088 others(4): Show |
7 | HG00558.hp1 HG01934.hp2 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.1254+68dupT | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr4 | 145554091 | ||||||
| chr4:145554091 | CT | C | 87 | a0001c0001t0001g0021 a0001c0001t0001g0043 a0001c0001t0001g0066 others(84): Show |
94 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(91): Show |
intron_variant | MODIFIER | c.1254+68delT | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr4 | 145554091 | ||||||
| chr4:145554335 | T | G | 1 | a0001c0001t0002g0177 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.1254+295T>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 6/6 | chr4 | 145554335 | |||||||
| chr4:145554423 | A | T | 1 | a0001c0001t0002g0015 | 2 | HG01981.hp2 HG02148.hp1 |
intron_variant | MODIFIER | c.1254+383A>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 6/6 | chr4 | 145554423 | |||||||
| chr4:145554652 | A | T | 1 | a0001c0001t0002g0177 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.1254+612A>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 6/6 | chr4 | 145554652 | |||||||
| chr4:145554825 | T | C | 90 | a0001c0001t0001g0009 a0001c0001t0001g0038 a0001c0001t0001g0094 others(87): Show |
97 | HG00423.hp2 HG00438.hp1 HG00621.hp1 others(94): Show |
intron_variant | MODIFIER | c.1254+785T>C | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 6/6 | chr4 | 145554825 | |||||||
| chr4:145555086 | T | G | 1 | a0001c0001t0002g0177 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.1254+1046T>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 6/6 | chr4 | 145555086 | |||||||
| chr4:145555089 | G | T | 1 | a0001c0001t0002g0177 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.1254+1049G>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 6/6 | chr4 | 145555089 | |||||||
| chr4:145555090 | T | G | 1 | a0001c0001t0002g0177 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.1254+1050T>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 6/6 | chr4 | 145555090 | |||||||
| chr4:145555469 | G | A | 84 | a0001c0001t0001g0094 a0001c0001t0001g0122 a0001c0001t0001g0138 others(81): Show |
90 | HG00423.hp2 HG00438.hp1 HG00621.hp1 others(87): Show |
intron_variant | MODIFIER | c.1254+1429G>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 6/6 | chr4 | 145555469 | |||||||
| chr4:145555494 | G | T | 1 | a0001c0001t0006g0219 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1254+1454G>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 6/6 | chr4 | 145555494 | |||||||
| chr4:145555552 | T | G | 1 | a0001c0002t0012g0052 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1254+1512T>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 6/6 | chr4 | 145555552 | |||||||
| chr4:145555559 | T | C | 1 | a0001c0001t0002g0169 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.1254+1519T>C | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 6/6 | chr4 | 145555559 | |||||||
| chr4:145555678 | TTACACTA others(22): Show |
T | 2 | a0001c0001t0003g0129 a0001c0001t0003g0238 |
2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.1254+1639_1254+166 others(33): Show |
SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 6/6 | chr4 | 145555678 | |||||||
| chr4:145555760 | A | C | 4 | a0001c0001t0001g0043 a0001c0001t0001g0066 a0001c0001t0001g0067 others(1): Show |
4 | HG02145.hp2 HG02451.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1254+1720A>C | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 6/6 | chr4 | 145555760 | |||||||
| chr4:145555761 | C | T | 4 | a0001c0001t0001g0043 a0001c0001t0001g0066 a0001c0001t0001g0067 others(1): Show |
4 | HG02145.hp2 HG02451.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1254+1721C>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 6/6 | chr4 | 145555761 | |||||||
| chr4:145555906 | T | C | 85 | a0001c0001t0001g0009 a0001c0001t0001g0038 a0001c0001t0001g0094 others(82): Show |
92 | HG00423.hp2 HG00438.hp1 HG00621.hp1 others(89): Show |
intron_variant | MODIFIER | c.1254+1866T>C | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 6/6 | chr4 | 145555906 | |||||||
| chr4:145556112 | G | A | 1 | a0001c0001t0002g0087 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1255-1679G>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 6/6 | chr4 | 145556112 | |||||||
| chr4:145556267 | A | G | 1 | a0001c0001t0002g0164 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.1255-1524A>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 6/6 | chr4 | 145556267 | |||||||
| chr4:145556278 | T | A | 85 | a0001c0001t0001g0009 a0001c0001t0001g0038 a0001c0001t0001g0094 others(82): Show |
92 | HG00423.hp2 HG00438.hp1 HG00621.hp1 others(89): Show |
intron_variant | MODIFIER | c.1255-1513T>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 6/6 | chr4 | 145556278 | |||||||
| chr4:145556307 | G | C | 4 | a0001c0001t0014g0076 a0001c0001t0014g0147 a0001c0001t0014g0148 others(1): Show |
4 | HG03453.hp1 HG03471.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1255-1484G>C | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 6/6 | chr4 | 145556307 | |||||||
| chr4:145556372 | G | T | 3 | a0001c0001t0006g0217 a0001c0001t0006g0218 a0001c0001t0006g0219 |
3 | HG01081.hp2 HG03942.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.1255-1419G>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 6/6 | chr4 | 145556372 | |||||||
| chr4:145556515 | G | A | 2 | a0001c0001t0001g0260 a0001c0001t0002g0179 |
2 | HG01261.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.1255-1276G>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 6/6 | chr4 | 145556515 | |||||||
| chr4:145556582 | A | G | 166 | a0001c0001t0001g0043 a0001c0001t0001g0066 a0001c0001t0001g0067 others(163): Show |
178 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(175): Show |
intron_variant | MODIFIER | c.1255-1209A>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 6/6 | chr4 | 145556582 | |||||||
| chr4:145556768 | A | G | 165 | a0001c0001t0001g0043 a0001c0001t0001g0066 a0001c0001t0001g0067 others(162): Show |
177 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(174): Show |
intron_variant | MODIFIER | c.1255-1023A>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 6/6 | chr4 | 145556768 | |||||||
| chr4:145556878 | A | G | 4 | a0001c0001t0006g0121 a0001c0001t0006g0126 a0001c0001t0006g0220 others(1): Show |
4 | NA18952.hp1 NA18973.hp1 NA18974.hp1 others(1): Show |
intron_variant | MODIFIER | c.1255-913A>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 6/6 | chr4 | 145556878 | |||||||
| chr4:145556905 | C | T | 13 | a0001c0001t0006g0119 a0001c0001t0006g0120 a0001c0001t0006g0121 others(10): Show |
13 | HG00738.hp2 HG01081.hp2 HG03654.hp1 others(10): Show |
intron_variant | MODIFIER | c.1255-886C>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 6/6 | chr4 | 145556905 | |||||||
| chr4:145557037 | CCTT | C | 84 | a0001c0001t0001g0094 a0001c0001t0001g0122 a0001c0001t0001g0138 others(81): Show |
90 | HG00423.hp2 HG00438.hp1 HG00621.hp1 others(87): Show |
intron_variant | MODIFIER | c.1255-751_1255-749d others(5): Show |
SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr4 | 145557037 | ||||||
| chr4:145557051 | C | A | 84 | a0001c0001t0001g0094 a0001c0001t0001g0122 a0001c0001t0001g0138 others(81): Show |
90 | HG00423.hp2 HG00438.hp1 HG00621.hp1 others(87): Show |
intron_variant | MODIFIER | c.1255-740C>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 6/6 | chr4 | 145557051 | |||||||
| chr4:145557068 | T | C | 1 | a0001c0001t0001g0066 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1255-723T>C | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 6/6 | chr4 | 145557068 | |||||||
| chr4:145557180 | G | A | 2 | a0001c0001t0018g0077 a0001c0001t0018g0153 |
2 | HG02895.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1255-611G>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 6/6 | chr4 | 145557180 | |||||||
| chr4:145557230 | A | G | 2 | a0001c0003t0012g0072 a0001c0003t0012g0144 |
2 | HG01884.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.1255-561A>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 6/6 | chr4 | 145557230 | |||||||
| chr4:145557315 | C | T | 87 | a0001c0001t0001g0094 a0001c0001t0001g0122 a0001c0001t0001g0138 others(84): Show |
93 | HG00423.hp2 HG00438.hp1 HG00621.hp1 others(90): Show |
intron_variant | MODIFIER | c.1255-476C>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 6/6 | chr4 | 145557315 | |||||||
| chr4:145557391 | T | G | 88 | a0001c0001t0001g0094 a0001c0001t0001g0122 a0001c0001t0001g0138 others(85): Show |
94 | HG00423.hp2 HG00438.hp1 HG00621.hp1 others(91): Show |
intron_variant | MODIFIER | c.1255-400T>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 6/6 | chr4 | 145557391 | |||||||
| chr4:145557513 | C | G | 13 | a0001c0001t0006g0119 a0001c0001t0006g0120 a0001c0001t0006g0121 others(10): Show |
13 | HG00738.hp2 HG01081.hp2 HG03654.hp1 others(10): Show |
intron_variant | MODIFIER | c.1255-278C>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 6/6 | chr4 | 145557513 | |||||||
| chr4:145557522 | G | T | 1 | a0001c0001t0001g0139 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1255-269G>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 6/6 | chr4 | 145557522 | |||||||
| chr4:145557627 | C | T | 225 | a0001c0001t0001g0009 a0001c0001t0001g0013 a0001c0001t0001g0021 others(222): Show |
242 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(239): Show |
intron_variant | MODIFIER | c.1255-164C>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 6/6 | chr4 | 145557627 |