| Tag | Content |
|---|
EnhancerAtlas ID | HS184-05631 |
Organism | Homo sapiens |
Tissue/cell | T47D |
Coordinate | chr11:61467110-61468300 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Klf1 | MA0493.1 | chr11:61467960-61467971 | AGGGTGTGGCC | - | 6.32 | | ZNF263 | MA0528.1 | chr11:61467387-61467408 | GAAGGAGGGTGGGGCTGGGGA | + | 6.54 |
|
| | Number of super-enhancer constituents: 12 | ID | Coordinate | Tissue/cell |
| SE_23644 | chr11:61462269-61469316 | Colon_Crypt_1 | | SE_23957 | chr11:61465178-61468528 | Colon_Crypt_2 | | SE_25088 | chr11:61465275-61469220 | Colon_Crypt_3 | | SE_27201 | chr11:61461011-61469578 | Esophagus | | SE_29301 | chr11:61465002-61469417 | Fetal_Intestine_Large | | SE_41676 | chr11:61465207-61469249 | LNCaP | | SE_47728 | chr11:61465812-61468584 | Pancreas | | SE_51045 | chr11:61461234-61469434 | Sigmoid_Colon | | SE_57966 | chr11:61466379-61467907 | VACO_9m | | SE_57966 | chr11:61468067-61468448 | VACO_9m | | SE_63420 | chr11:61457154-61498627 | NCI-H69 | | SE_65661 | chr11:61460755-61471450 | Pancreatic_islets |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | CCTGTTCTTC CCTGCGCTGC TTCTGTCACC TCACAGTCAG GCCCCTCCGG GGAGTACAGT 60
GGAGGGAAGG CCAAAGCATT CATCCTGGAA GACCCTCCAA ATACTGTAGG CAGAGTGCTG 120
GGGACACCAA TGGCAGCTGT GGGCAGGGCC ACCCGAATGC CACCCCATAG GGCAGCGGGC 180
CCACAGCATG GAGGCCCTCC GTGTTTGCTT TTCCCAGCCC TGCATTAGCT GTGCTGCTCA 240
CACCTGGCTG ACTGTTTGCC CAAGGATTTC TCCCCTGGAA GGAGGGTGGG GCTGGGGAGG 300
GTGGCAGGCA GGTGGCCGGC TGCCTCTGGG CACTCCGTTT TTCTGCAGAC CCACACTGCC 360
TGCGAATGCC ACACCACCCT GCATCCCCAA GGCTGCCCCA GCAGTGCCCG GCCTCGCCCG 420
CGCAGAGCAT GTGACTTGGC AGTGCCTGGG CCTGGCATGC CTGGCGTGCC AGGGCAGCGG 480
CAGCAGCAGC CGGACTGTCA GTAAGGAGCT GGAGAGGCCC CCAGAGCCCT CCTGTTGGGG 540
CACTGGTCCT GGGTTGTGGG GGTGACGGGA TGCATCAGTG AGACTTTTGT ATGGCAGGAG 600
GCAGAGGAGC ACATAACTGA ATCTGGGAGT ATTTATGGAC ACGTCTGCGC CTTCCTTTTC 660
TGCAGCAGCC TGTCTGCAGG CCCTCCTGCA AGGAGAGCCT GTCTTGATTC AACCAGTCCC 720
TGCCCTGACC TTCTCTTCAC CCTCTTTCTG ATGAGTCAGC CCCAGGAACT TGAACTTGGA 780
CTTCTCCAGC CTCTGGGCCA GCCCTGGAGG CGGAAGCCCT GGACCTGCCT CCCCAACACC 840
TGCCCTCCTG AGGGTGTGGC CTGCAAGCGT CCTTTTCTGT CAGATTCAGC TCATGGCCAG 900
TGACTCCTTG AGCCTGTGAT CGTGGTCCTC AGGCCAAGGG GAACAGATTA GATAATTAGC 960
TGCTGATGGA TCTGGCATCC TAGGGAAGAG GGAGCCCTTT CTCTCCCACA GCTGGGACCC 1020
CAAAGAGAGG CTTGCATTAG CCAGGCAAGG AGCCGGGTGC CTCCCTCCCT GCAGTCCTGC 1080
ACAGCCCCTT CCTTCTCTTG CTGCTGTGGG TATCTGCCTA AGGAGAGCTG GCCCAGCATA 1140
CCCACCTGGG ACACACCCAG AGAGTGCCAG CCTGAACGGC ACTGCCAATA 1190
|
