| Tag | Content |
|---|
EnhancerAtlas ID | HS130-19977 |
Organism | Homo sapiens |
Tissue/cell | MDA-MB-231 |
Coordinate | chr4:160281400-160282780 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Esrra | MA0592.2 | chr4:160281667-160281678 | TTCAAGGTCAT | + | 6.62 | | Esrrg | MA0643.1 | chr4:160281668-160281678 | TCAAGGTCAT | + | 6.02 | | JUN(var.2) | MA0489.1 | chr4:160281852-160281866 | GTGACTCATTTCTT | - | 6.15 |
|
| | 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 |
| GH04I159360 | chr4 | 160281321 | 160282571 |
|
Enhancer Sequence | GATTTAGCCT CATGGTTATT GGAAACTGCC CAATAGCCTA TTTATTTTAG GCAGATCTCT 60
GTTGATCCAA AGCAATTAAT ATCATTAACG TTAGCACCAG CCAAACCATG TTCAGAATTC 120
AGTGTTTCTT GAAAATGAAG ATGCTGTCAC AATATATTTG CATAACATTT GTCTCTTCTC 180
AACCGTTTCC AACAATAATC TTTATGGTAC GTAATATTTT GGTTCCCAGT ATACATACTG 240
AGAGACAGGA CCTCAGAGAA ACTGACATTC AAGGTCATGA TTATTAAGTG GAGAGTACAA 300
TTTAGCTAGT GATTCTGGAC TTCTAACTAG TACACAATAT GAGTGCTGAT GTGTGGTAAG 360
TCTGAATAAT ACTTTAGTCT ATCAGAAGGG CACTTAATTT TAAAAGGTAA AAACCAGTAA 420
GTAGCAGCCT GCTTACGCAC ATGTTTAAAT GAGTGACTCA TTTCTTTTCC TCAAGCAAGC 480
ATAACTAAAA GTATTAGCCA TCAGCCACTG AGAAGTCTCA GAAGTCAGAG TGGAAGCAAC 540
TGGAAGCAGA GGCACCAAAC ACTGGAACAT GTGAGGGAGC CTGAAGAGGA GCGGGAGGAA 600
GGTCCCTCCA GAAGCTAACA GGAAAATGGC CAGGGCTAGG CTTCAAGATC TTTCCAAGGT 660
ATTCGTGCCA GCTATTTTGC TGAGAAATTT TGAAAACCTG GACACCAAAA TAGTCGGGAA 720
AATTATTTAT TTATTTATTT ATTTATTTAT TTTTTAACCA TTCTAGTAGC TTCAACCACA 780
CCTTTTAAAA AATGAAGAAC CTGCGTGTTT GTGTATGTTG TTACATGCTC ATCTCTGTTG 840
TCTTTTCACT TTAAAACCCA TTCCTCAGGG ACTTTCCTAG ACTGTCACTC AGCTTAATTT 900
TCTCAAACTT TTTTTGAAAA AATACTAAGA ATCTGATGTT TTGGAGAATA ACCTCTTTAT 960
CATTACTGTG TGTGTTCTGC TAAAAATATG AGACAGTGAC AAATAGGGCA TGGTTCGTTT 1020
TCCTTTTAGG TTTTATTAGA CTTTTATGTT TTAGGATACT TCCTCCGTGT AGCACAAGAC 1080
TGGTCTCCAC TTAAGGGTTT CCAGAAATAA GTATTTGCCA AGTGTAACAG TTTGCAGGGA 1140
CAGAGTTTAT GTTATGTTAA TAATAGAACT TTGCCAAGTT TTAGGGATAT TGTAGAAGGT 1200
TTTGGTGAAG GTCTGATGCT CTCCACCCTA ATCAAAGAGG CCACACAGAC CGGGGTCTGT 1260
GTTTTCATAC ATACAGGTTG AAGTCCTCAG AATGTTTTTC TCAGCCTCAA TCCATTTCTC 1320
TGCTTTTGGG AGGTATAGAT TTTATGCTCA TCTATGATTT AATATGTTTT ACCTTTAGTT 1380
|
