| Tag | Content |
|---|
EnhancerAtlas ID | HS130-00315 |
Organism | Homo sapiens |
Tissue/cell | MDA-MB-231 |
Coordinate | chr1:17613630-17614620 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NR2F1 | MA0017.2 | chr1:17614474-17614487 | CACGTGACCTCTG | - | 6.04 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH01I017286 | chr1 | 17613436 | 17614463 |
|
Enhancer Sequence | CTGAGCACAT AACTTGGGTG AGCCTCAGTT TCCCCCTCCA TAAAATGGGC AAAATAACTG 60
CCGCTTCATA GAGCTTGCAT GGGGATGAAG TAGGGTAACT CACAAGATAT ACTTAGTGTC 120
AATAGCACAG TGCATGGTGC ATAGTAAGTG CTCAGTAAAT GATGACTGCT GTTACATAAC 180
ATCCCCCAGC CCTTCCTCAA GCATCTGCTG TGTAGAACAC TCCTAATCTC CGCGCTTTAA 240
TAGATGACAA AGACCCTTTG AGACCCAGAG GTGAAATGAG GGAGGTAGGG ACAGGACAGC 300
TGTCTTGGCT ACTCTCAGAT CATACCCTGC TTGTCTCAGC TGTGTAGGAC TGGCCCAGGT 360
GGAGGCTCCT GCCTGGACAA GAAGCTGACA AGAAAGCCTG TCTTTTTTGT GGGGATTTGC 420
AGCTCTGGGT GGCCCTGACT CATGCTTTAT TCAGAATTTG GAATAAGTAG CTGCAGGGCT 480
TCCGCAGGCA TTGCCCAACT CTGTGGCCTC CTGCGGCTTC CAGCAGCCCA GGAAGGAGGG 540
CCCTGGGTGA GGATGGCTGG AAAGGAATTC TGGATGGCTG GACAGAGTCC ATGGGACCTA 600
TCACTTCCTA CAAAGTCACT GTCATCCCAA GTCCCCTCCA GCATAATGAC GGCAAGTGCA 660
AGCATTGTGC CAGCAGGTAC TGAATGCTTC CTGAGCACCA TCTGATATAG CCCTCACAGC 720
ATGCCAGCAG GCAGCTATTA CTATTGTTCT CACTTTATAG ACAGGGAAAC TGAGGCACAG 780
CCACATGAAA GCGCTTGCCC TGGTCACAGA GCTATTAAGT GGGGGAAACA AATTTGAGCC 840
TAGACACGTG ACCTCTGTAC CCAGTCACAC CAGTGGTTCT CAACCCATCT ACACATTAGA 900
ATCACCTGGA AGGCTCTCAT GAAAACCTAG CAGGGCCAGG CCCCCACCAT CAGAGATTCT 960
GTCTGGACAT TGGGATGTTA CACAAAGCAA 990
|
