| Tag | Content |
|---|
EnhancerAtlas ID | HS130-06138 |
Organism | Homo sapiens |
Tissue/cell | MDA-MB-231 |
Coordinate | chr11:129705520-129707330 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Gata4 | MA0482.1 | chr11:129706417-129706428 | TCTTATCTCCC | + | 6.62 | | PHOX2A | MA0713.1 | chr11:129706473-129706484 | TAATTAAATTA | - | 6.62 | | PROP1 | MA0715.1 | chr11:129706473-129706484 | TAATTAAATTA | + | 6.32 | | PROP1 | MA0715.1 | chr11:129706473-129706484 | TAATTAAATTA | - | 6.62 | | Phox2b | MA0681.1 | chr11:129706473-129706484 | TAATTAAATTA | - | 6.62 |
|
| | Number of super-enhancer constituents: 5 | ID | Coordinate | Tissue/cell |
| SE_27353 | chr11:129705074-129706482 | Esophagus | | SE_27353 | chr11:129706483-129707258 | Esophagus | | SE_35121 | chr11:129704672-129707645 | HeLa | | SE_36539 | chr11:129705094-129707307 | HMEC | | SE_64293 | chr11:129705014-129707335 | NHEK |
|
| | 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 |
| GH11I129835 | chr11 | 129705254 | 129707310 |
|
Enhancer Sequence | ACCTTGGGCC CAGGCACACA GATTCAGGGG CAGGTCTGGT GCCACTTCCT TGGTTTCAGC 60
AGGCCAGGAT GCCCCAGCCC AGGACCAAGG GGTGGGGCCA GCATTTAGGG TAGAGGAATC 120
AGGGTGATGG CCCTGGAAGG CAGGGCCACC CTGTGGACCC AGACAACAGA ACACTGAGCC 180
AAAGAGGATT ATTCTCAAGC CTTGGCATTG GGCTGGGCGC AGTGGCTCAC GCCTGTAATC 240
CCAACACTTT GGGAAGCTGA GGCAGGTGGA TGACCTGAGA TCAGGAGTTG GAGACCAGCC 300
TGGGCAACAT GGTGAAATCC CGTCTCTACT AAAAATACAA AAAATAGCCT TGCATGGTGG 360
CTCATGCCTG TAATCCTAGC TACTTGGGAG ACTGAGGCAG GAGAATCACT TGAAGCCAGG 420
AGGCAGAGGG TGGAGTGAGC CAAAACCGCG CCATTGCACT CCAGCCTGGG CGACAAGGGT 480
GAAACTCCAT TTCAAATTAA AAAAAAAAAA ATTGAACGGA ATTTGCCCTA CCAGGTTCCA 540
GGACAGGAGA TCCATGACCA CTTTCTTCTT TCCAATGTCC CACTTTTAAA CTAGAAATGT 600
CTATGCTCTG CCTGTCCTGT TTGGGAAGCA GATAATTTCT TGTCTGGTCG TAAAGGTTCA 660
CAGCTGGAGA ATTTTGCCTC AGGATGAACC ATACCTCAAA TCTCACCCAT ACCTGGTTTA 720
GACGATACTT ACATGAGATT TGGGACTTAA CAGTTGATGC TGATCTGGGT TAAGACTTTT 780
GGCACTGTAG GGATGGGGAT AAGTGTATTT TGCATATGAG AAGGATATGG ATTTTCAGGG 840
AGCAGAGGAC AGGGTGTTAT GGGCTGAGTG TGCTCTCTCC AAATTCAAAT GTTGAAGTCT 900
TATCTCCCAG TACCTCAGGA TGTGACTCTT TTGAGATAAG ATCTTTAAAG AAGTAATTAA 960
ATTAAAATGA GATCATTAGG GTGGGGCCCA AATGCAGTAT GAGTAATGTC CTTATAAGAA 1020
CACAGACACA CACAAGAGGA CGACCATGTG AGGACACTGA GAGAAGATGG CCATCTCCAA 1080
GCCAAGGAGA GAGGCCTCCA GAACTGAGAA TATAAATGGT TGTTTAATCT GCCCAGTGTG 1140
TGGTACTGTG TTACCAGCCC TAGCAACCAG TGTATGTGGT CTACCCACAC AATGAAATAC 1200
CATTCAGCCA TCAAAAGGAC TCAGTGGTGA TTCATGCTTA CAACATGGAG AAACCTGGGA 1260
AACATCGTGC CAACAGAAAG GGCCAGTCAC AAAAGGCCAC ATATTATATA ATTCAATTTA 1320
TGAATTGAAA GGCAAACCTG TAGAAATATA AAATCGACTG GTGGCTGCCT GCTGGACACC 1380
CCGCAATGTG CAGGACGGCC CCACAACCAA GACCCCTGTG GCCCAGAGTC TCAGCAATGC 1440
CGAGGCTGTG AGATCCTGCT CTCGCCCAGG CCTGCTTCCC AAAGCCCTTT AGTCCTGAAG 1500
GGAGAAGAGA ACAGGCTGCC TTCTTTCTTT GTTATTGAAA TCCCACTTAC TCCCTCTTAC 1560
AGCATGCTCT TCTCCCTTTA AGACCAGCCC GGGCTGGTCT CTACCACGTG TAGATAGGGC 1620
TGGGGAAGGA GAAGACTGGT GAGAGTGAGG GGTTTCTTTT TTTTCTTTTT TTTGTTTTGA 1680
GACGGAGTCT TGCTCTGTCT CTCAGGCTGA AGTGCAGTGG CGCCATCTCA GCTCACTGCA 1740
ACCTCTGCCT CCCGGGTTCA AGAGATTCTC CTGCCTCAGC CTCCTGAGTA GCTGGGATTA 1800
CAGGTGCCCA 1810
|
