| Tag | Content |
|---|
EnhancerAtlas ID | HS184-24661 |
Organism | Homo sapiens |
Tissue/cell | T47D |
Coordinate | chr5:125689580-125690730 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chr5:125689775-125689794 | TATCCACTAGATGGTGCCA | + | 6.14 | | Foxd3 | MA0041.1 | chr5:125690459-125690471 | GAATGTTTATTT | + | 6.74 | | Klf1 | MA0493.1 | chr5:125690677-125690688 | GGCCACACCCT | + | 6.32 | | RUNX1 | MA0002.2 | chr5:125690163-125690174 | GTTTGTGGTTT | + | 6.02 | | STAT1 | MA0137.3 | chr5:125690186-125690197 | TTTCCCGGAAA | - | 6.32 | | Stat4 | MA0518.1 | chr5:125690183-125690197 | TCCTTTCCCGGAAA | - | 6.78 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_37246 | chr5:125686573-125692694 | HSMMtube |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr5 | 125689584 | 125690527 | | chr5 | 125690030 | 125690185 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH05I126352 | chr5 | 125688050 | 125692088 |
|
Enhancer Sequence | CACAATCAAT TAAAACAGAA TCACCTGGGA AGCTTGTTAA AAAAAACTCT GATGCCCAAG 60
TCTCACACCA AACCTATAAA ATCAGAATGT ATAGGTGTGG GGTATTTGTA CAAGTTCTGT 120
GCAATTGTGA GGCATACTAA GAAAGTTTGA GAACCACCAT TTAAGAAAAT AACTGGTCTC 180
TAAATTAGGA CTCATTATCC ACTAGATGGT GCCAAGAATT CAAAGATGGA ACTTTGTGGT 240
ACAATGTCTA TTTTCCTTTG AGTATACAGT GTGTTCATTT TCCTTCTTAT CCACTTTCTC 300
TTCGACCTCT CCCCAACTTG TAGGAAAGGG TTACATCACA CCAAAATAGA TATTTTGTTC 360
AGTATCAGTC TAGCAGCTTC TCCTTGGATT TTGGTTATAA CAGACAGGCT CGTTCTGAAG 420
GGATATTGAG AGGAAGTTGT GTGAGTACTC TTCCCTTAGC CTTTTACTTT CTCAGTGCAG 480
ATATTTAGAA GAGGAAAATC CACTGTAAGA GGTGGCCTCA TTGGCAATGA GTGATTGGAT 540
AAGAAAGAAT GGTCTGACCA GTTCCTAAAA GCCATATTTA GCCGTTTGTG GTTTTGATCC 600
CTGTCCTTTC CCGGAAACAA TGACTTCAAG AATGTACCAC AACTATTTGG TATGTTATAT 660
CAGTTAAATA ATAAGTCATA TTATTAAATA TCAGATTACT CTTAAGCTAC CACTGCCTCA 720
ATGGAAAAGC ATTTGACAAT TTCTTAAACT GTTTTATCCT TTCTTTATCC TCAGGATTTT 780
TGCAATTAAA AAATCCTGTG CAGATGATAA TCTCATTTCA GTTTTTCTGA TGAGTTTATG 840
TGTTTGGAAT CTGCTCCAAG GCATTGTGTT TATCCTCATG AATGTTTATT TTTAAATGTG 900
TATCGAATAG AAATGGCTAG AAAGCCGAGC AAGACAAATA ACATTTTATT AATCCTTGTC 960
TTAGTCTCTT TGTGCTGCTA TAACAAAGTA CCTGAGACTG GGTAATTCAT GAAAAAAAAA 1020
AAAAAAAAAA AATGTATTTT CTTACCATTC TCGAGGCTGG GAAAGATCGG GGCACTGGCT 1080
TCTGATGTGG GTTTTTTGGC CACACCCTCA CACGGAAGGA GGAACAGGGG CAAACTAACT 1140
AAACAGTTCA 1150
|
