| Tag | Content |
|---|
EnhancerAtlas ID | HS183-01308 |
Organism | Homo sapiens |
Tissue/cell | T47D-MTVL |
Coordinate | chr12:110781690-110782690 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| TCF7L2 | MA0523.1 | chr12:110782590-110782604 | TGTCTTTGATCTTC | - | 6.41 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_26768 | chr12:110779806-110784507 | Esophagus |
|
| | 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 |
| GH12I110343 | chr12 | 110781648 | 110784256 |
|
Enhancer Sequence | TCTTCCCCAT TTCATAGATT GGGAAAGTGA GGTGAAATCA CTTCCCTGGG ATCCCATAGG 60
AAGGCATTGT GTTTTCATAA TATATTCACA TGACTTCAAA TTCAAAAAGC ACACAATGGC 120
ATAGAATGGA AAGGGTTTGG GCCAGTCACT TCCCTCTGGC GTTGAGGTGC TCATGTACCC 180
TGTGCCCTTC CGGAGAGATT CCAGCATGCT GTGCACACCT GCATGTTGAC CCTTGTCTTG 240
CCTTCTTCCT GCTTGTCAGA TCCTTCCATA TCCGGACATG CGTAGTGCCT CATCCTTGCA 300
GCCAGCGGCC TTCATGCTCC ACTGTAATTC GTGGGTTAGT GGGTATATGC ACTTGTTGTT 360
TTTGATGCTA CCACATGGGG ATATTTGCCT CGTCTGAACT CTGTGTATTC TCTGCTGCAC 420
CTTGTTGCTT CTTTGCAATA AACTTCCTGA ACTCAAAGCT AATACTGGGG GGAATCCCAG 480
AAGCTGCTGA GGGCAGGGCC ATGCTGCTCA GTGTTCCACC CTAGCTCCTG ACAGCATTTC 540
CCTAGAAAAC TGCTGCTGGG CCTCTAATGG AGCAAATAAA TCTGTGTACA ACTAGGCAGC 600
AATAGTTTGT CCAAAAGTCC TGGTGTAATC TAGTCCCTCA AACTGTGCAG CCTTACATGG 660
AGTACACACA CACTTGCAGC CTTGAAGTAC TACCCACTGA GGGGAGAAGG CACGGCAAGG 720
GGAAAGGTTG GCACAGGATG GAGCAAGTGC TTTTTCTCAC ACATTCTGGA GGAAAAGTTA 780
TCCAGTTCTT CTGTTCTAGA AACACCCCTG TCCTTCAGAA ACCAGGGTCT AGTTGCTCTG 840
GCTACCAGGC GTGAGCAGGT GGTGGTAGCA CCACAGGCCC CGGTTACCAT CACTGTCCCA 900
TGTCTTTGAT CTTCGTCCTT GTGGGGACTG GCCTGCATGG CCTCGGTGGC AGCGAGCCCT 960
GCAGAGGCAA GTGCATCAGC ATCACTGTGT TTGTTCCCAG 1000
|
