| Tag | Content |
|---|
EnhancerAtlas ID | HS184-05531 |
Organism | Homo sapiens |
Tissue/cell | T47D |
Coordinate | chr11:57060340-57061410 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NR2F1 | MA0017.2 | chr11:57060541-57060554 | CAGAGGTCAAAGG | + | 6.74 | | RREB1 | MA0073.1 | chr11:57061048-57061068 | ACACCAACCACCACCACCCC | + | 7.77 |
|
| | Number of super-enhancer constituents: 9 | ID | Coordinate | Tissue/cell |
| SE_26710 | chr11:57060169-57063674 | Esophagus | | SE_31504 | chr11:57060367-57061489 | Gastric | | SE_36201 | chr11:57060237-57063633 | HMEC | | SE_37251 | chr11:57058985-57064256 | HSMMtube | | SE_42553 | chr11:57060659-57061600 | Lung | | SE_46610 | chr11:57060093-57063560 | Osteoblasts | | SE_55925 | chr11:57060225-57063451 | u87 | | SE_64652 | chr11:57060105-57061540 | NHEK | | SE_67692 | chr11:57060225-57063451 | u87 |
|
| | 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 |
| GH11I057291 | chr11 | 57059473 | 57064353 |
|
Enhancer Sequence | AGGCGGAGCT TGCAGTGAGC AGAGAGCACG CCACTGCACT CCAGCCTGCG CAACAGAGCC 60
AGACTCCGTC TTAAAACAAA ACAAACAAAA AACAAAAAAA CACCTTATCG CTCTGCACCC 120
AGGGCCTGGC ACTCTCCCCG GGGGAGGGCG GTGTGCTTCT GAACCTGCCA GCATTTTTTC 180
TATCTATGAT ACACTTGCTG ACAGAGGTCA AAGGGCTATC CTGGGTAAGC CCACACTGCT 240
GGCTCAAGAG GCCCCAGGCA AATCAGCCCC AGGAAAATCT CGTCCATCAG CTTCTAGGCC 300
AAGCCTCAGC CTGCTCTGTG TCATCAGTCT GGGAGGCAGG AAGACTGCAA AGGGTTCTCA 360
GTTCACCATA CGAACAAAAG ACAAGACGAG ACTCGCCAGG AATGTGTGGT TTGTCCCAGG 420
CACTTTGTCC TGCATCCAGA CCTCAAGCAG TCAGATAAAG CTGATTCTTT ATTTTTGCAC 480
TTCTTTTAAA GCTCAGGCTC AGAGAGAGAG TCCCCAGCTC ACAAGAGTCA GAAGCAGGAT 540
ATAAACTCTG ATCTACTCAC TCCAGAGCTG CCCGCAAGAA GGACACCTGT CTCTACCCAT 600
CTCGGGAATG TGCCATGACC ACAGCAGATG GCTGGACTAC GTTTAGGAGA CAGGATGCTG 660
GAGAAAGGAA GTGTCAAGCA GTGGGCAGCA CCCTTCAGAC CTCCCCTGAC ACCAACCACC 720
ACCACCCCAA TACTGAGGGC TCCATGGACA AAGGCCAGCT CGTTCTTGGG CCCAAACACC 780
AGTTGCAGCT CCTGGATCCT GGGAAACGTG GGAGAGCACC AGTGACTGCT CCCTGGGCTC 840
CACTGCTGTT CCATTCCCAA GGGCATCCTC CATCATCCTG GTGTCCAATT CCTAGGCAGA 900
CAGGCCCTCC CCTTGCTGAG GACCTCCAAA GCAGGGGCCA GGAGAGAGAC GGTGCTGAGA 960
CATTTCTCAC TGTAATTGCA TTGGGACCAG ATCCTTTCTC TCTCTGAGAG TTGGCAACAA 1020
GAACCCCCTG GGAGGAACAA CAACTCAGCT TTCTAACAGG TAGCCTTCTT 1070
|
