Variant report
Variant | rs6414229 |
---|---|
Chromosome Location | chr3:94678116-94678117 |
allele | C/T |
Outlinks | Ensembl   UCSC |
- TF binding region (count:16)
- CpG islands (count:0)
- Chromatin interactive region (count:0)
- LncRNA region (count:0)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
(count:16 , 50 per page) page:
1
No. | Transcrition factor | Chromosome Location | Cell Line | Cell type | Cell Stage | Matched TF binding sites |
---|---|---|---|---|---|---|
1 | TCF7L2 | chr3:94677933-94678236 | MCF-7 | breast: | n/a | n/a |
2 | GATA3 | chr3:94677955-94678451 | MCF-7 | breast: | n/a | n/a |
3 | HDAC2 | chr3:94677991-94678319 | MCF-7 | breast: | n/a | n/a |
4 | GATA3 | chr3:94677891-94678349 | MCF-7 | breast: | n/a | n/a |
5 | GATA3 | chr3:94677742-94678462 | MCF-7 | breast: | n/a | n/a |
6 | CEBPB | chr3:94677923-94678286 | MCF-7 | breast: | n/a | chr3:94678081-94678092 chr3:94678080-94678093 chr3:94678080-94678091 chr3:94678080-94678093 |
7 | NR2F2 | chr3:94677942-94678332 | MCF-7 | breast: | n/a | chr3:94678307-94678322 |
8 | ZNF217 | chr3:94677936-94678380 | MCF-7 | breast: | n/a | n/a |
9 | TCF12 | chr3:94677731-94678486 | MCF-7 | breast: | n/a | n/a |
10 | CEBPB | chr3:94677790-94678168 | HepG2 | liver: | n/a | chr3:94678081-94678092 chr3:94678080-94678093 chr3:94678080-94678091 chr3:94678080-94678093 |
11 | GATA3 | chr3:94677959-94678257 | T-47D | breast: | n/a | n/a |
12 | EP300 | chr3:94677961-94678335 | MCF-7 | breast: | n/a | chr3:94678078-94678092 |
13 | CEBPB | chr3:94677749-94678401 | MCF-7 | breast: | n/a | chr3:94678081-94678092 chr3:94678080-94678093 chr3:94678080-94678091 chr3:94678080-94678093 |
14 | CEBPB | chr3:94677717-94678167 | IMR90 | lung: | n/a | chr3:94678081-94678092 chr3:94678080-94678093 chr3:94678080-94678091 chr3:94678080-94678093 |
15 | SIN3AK20 | chr3:94677858-94678332 | MCF-7 | breast: | n/a | n/a |
16 | GATA3 | chr3:94677828-94678336 | MCF-7 | breast: | n/a | n/a |
No data |
No data |
No data |
No data |
No data |
Variant related genes | Relation type |
---|---|
LINC00879 | TF binding region |
rs_ID | r2[population] |
---|---|
rs1579543 | 1.00[EUR][1000 genomes] |
rs16853923 | 1.00[EUR][1000 genomes] |
rs28682536 | 1.00[EUR][1000 genomes] |
rs4384951 | 1.00[EUR][1000 genomes] |
rs57431896 | 1.00[EUR][1000 genomes] |
rs58014210 | 1.00[EUR][1000 genomes] |
rs58086527 | 1.00[EUR][1000 genomes] |
rs59975236 | 1.00[EUR][1000 genomes] |
rs60472824 | 1.00[EUR][1000 genomes] |
rs73847076 | 1.00[EUR][1000 genomes] |
rs73847085 | 1.00[EUR][1000 genomes] |
rs73847088 | 1.00[EUR][1000 genomes] |
rs73847092 | 1.00[EUR][1000 genomes] |
rs73847093 | 1.00[EUR][1000 genomes] |
rs73848726 | 1.00[EUR][1000 genomes] |
rs73848727 | 1.00[EUR][1000 genomes] |
rs73848734 | 1.00[EUR][1000 genomes] |
rs73850322 | 1.00[EUR][1000 genomes] |
rs7628702 | 1.00[EUR][1000 genomes] |
rs973259 | 1.00[EUR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv877169 | chr3:94675697-94840854 | Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS | TF binding regionChromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | diseases |
No data |