| Tag | Content |
|---|
EnhancerAtlas ID | HS184-05617 | Organism | Homo sapiens | Tissue/cell | T47D | Coordinate | chr11:61269790-61271060 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| SPIB | MA0081.2 | chr11:61270791-61270803 | AAAGGGGAAGTG | + | 6.07 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | CAAGCAGAGG GACTGGCATG TCCAAAGGTC CTGGGGTGAA AAGAAGCTCT TCAGGTTAGC 60
TCATCTCCAA GTGGTGACTC TGGGATCCAG GATCCTTTCC ATCTTTAACA TCACAGTAGA 120
TAAATGGAGC ATGGAGGATT GTGCATTCAT GTGGTATGTT TCACTTCTGC CCACATCCAT 180
TAGCCCAGCA GTCATCCCAG GGTCTTACCC TCTCAGCTAG GAAAAGTAGT TTTACTGAGG 240
GCTCAGGAAG AAGAGGGGGA AAAAACAGAA GTTGGTCACT CTCAGTAGCC TCTGCCCCAG 300
GGGGACCAGG CCAGACAAGT CCTTGGTAGT CTTGGTTGGG ACCTGGATCT GTATTCTTGG 360
AGCAGATGAT CTGATTTGCA TTTGGCCACA GATCCAAGAA GGTATTAACA TAAAGAGCGA 420
CTGCCAGCCA TGACCCCAGC ATTCCTCCCA GGAGGAAGGA GTCATCAAGT CCACTTTGTA 480
GCTTGATGGC CTAACAGAAC CCACTGGGGT GGTCAGAGTT CCATCCACAA CATTCTGGAA 540
TGTGGCCTTG GGAACCAGTC AGCTTCTCCC CCTCCTCACA CTCCTGTGGC CTCTGTTGCT 600
CCAGCTCTGG TGTCTCTGAG GGGGACCTGG GAGGACTCTC AGCTTTCAAC AGATCAGGCA 660
GGTAACTCAC AGAGCTAGGG TTCCAGGTAA ACATGATCCC CAGGCCACGC CTGGGCTCTG 720
GTTTCTTAGG CAGGATGGGA GGAGTAGGTT GGCAGTGGCT GAGCCAGCCT GGTGAGTTTG 780
GCTATCACTG ATGGGCTCTA GTCTAACGGT GGGCCAGAGA CTGCCTGGAA TTTGGTATCA 840
TATAAGCCCT GAGCCCAGAT CACAGGCCTA GGATGACCCA GGACCTGGGG ACCTCTTTGT 900
TCTGTCTTGT GGGACCTGAT TTGGGGTTCC TAGGCTTGCC CTGTGGATTT CAGGATACCC 960
CCTAGTTAGG CAAACATATG AGCCCTGGGG CCTGGGATGG GAAAGGGGAA GTGGTGTGGC 1020
TCATAGCCAC TCTTGTCCTC TCTGACAACA TCAAAACCTC CAAGCAGGGC ACCCCTAGAA 1080
ATATTTTTGC TGTTTGCAGG ATGGAGGTGA GCGTTTGAGC ACCCAGGGTG GTTTCTCTAA 1140
TTTCTCCTAG ACCACAGAGT CAATGAGACA TCGTCGACAA AGCCCGGGCT TTGCAATAAG 1200
ATGGACTGGG TTTGAATCCT GGCTCCGCCC CTTACCGGCT GTGTGACCTT GTAGCTTGGC 1260
AGTGGCTGTT 1270
|
| |
|
|
|
