| Tag | Content |
|---|
EnhancerAtlas ID | HS101-11510 |
Organism | Homo sapiens |
Tissue/cell | HT29 |
Coordinate | chr12:120831750-120833120 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EN2 | MA0642.1 | chr12:120832754-120832764 | GCTAATTGGG | - | 6.02 | | ZEB1 | MA0103.3 | chr12:120832654-120832665 | CCCACCTGCCC | + | 6.14 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_65438 | chr12:120831662-120833343 | Pancreatic_islets |
|
| | 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 |
| GH12I120394 | chr12 | 120831965 | 120833250 |
|
Enhancer Sequence | ATCTTCCCAC CTCAACCTCC CAAGTAGCTG GGACCACAGG CACGCACCAC CACACCTGGA 60
TAATTTATTT TATTTTATTT TTATGTTTTG AGACAGAGTC TTGCTCTGTT GCCCGGGATG 120
GAATGCGGTG GGGCAATCTT GGCTCACTGC AACCTCCACC TCCCGAGTTC AAGCGATTCT 180
CATGCCTCAG CCTCCTGAGT TGCTGGGATT ACAGGCGTGT GCCACCACGC CCAGCTCATT 240
TTTGTATTGT TAGTAGAGAC AAGGTTTTGC CATGTTGGCC AGGCTGGTCT GAAACTCAAG 300
TGATCCTCCT GCCTTGGCCT CCCAAAGTGC TAGGATTACA GGCATGAGCC ACTGCGCCTG 360
GCCCAGTTAC TTATTTTAGA AGTTATATTT GAGCACCTAT TCTGTGCCGA GCCCTGGCAT 420
GAGCTGTGAA CAGGCCATAT CTATCCTAGA TGTGCACTAA TGGGGCTTTG GAGGGTGGCA 480
ACAGGAGGCC CGGTGAAATC CCCGGTGAGA GCAGCCTTTT CGCCGTGGCC TGCCGTGAAG 540
CACTATGGCA GCACCCACAC CTGCCAGGAC TGAAGGTATT GTCGGGCCCT CTCCTGCTCC 600
CAGCTGCAGC CAAGGCCGTG TGTACAGGGC CCTTTAAGTA GTCTGTGCCC TCCCTAATTA 660
ACCAGCTAAA GAAAGAGCTG GCTTGAAATG GGATTGTGCA GACCCAGCTT TGGGACCCGA 720
GGACGCCGGA TCGGGGATTG TTATGCTAAT CGCCTGAGAT CAGCAGTTCC CGTGCCCTTC 780
AGATGGCAGG TAGCGAGGCC GGGCTCTGCC CAGCGGCTGT GGCTACAGGA GGCCAGGCTT 840
TTCCTCCAGC TTCCGGCTTC CTCTGTTCCC CTCCTTACCC CGTCAGACTT GCCCTGCCTG 900
TCCTCCCACC TGCCCGTTGG CTGGAAGGCT TGGCGTCTCC TAGAAATGTC CAGGCCAGCT 960
CCTCCCACCC TCCAAAGAGA AACCTGCTTG CCTTCAAGCT GGGCGCTAAT TGGGGATGCA 1020
GAGGCAGGAA GGAGAAGGTA CCCAGCTCCT CCTCCTGTAT AACCCATTCT CATCTCCAGG 1080
CATGAGAGCC TCATTGGTCC CTCCTGCCCC CTTGGGCTCT GGAAAACACA CTAGGTGGTG 1140
CCTTTGCCGC TTACTAACTA TACCATTTTG GGCAAGTGAC TGCCTCTCAG AGCCTCAGTT 1200
TCCTAATCTG TAAAATAGGT TGATAATAAC AGTAGCTACC TCAAAGGGTT GAAATGAGAA 1260
TAGAATGAGA ACAGGCATCT AACATAGCCA GTTCAATTGC TACTGCCCAT CCAGCACTGG 1320
ATAATAGCTC CCTGTGTAGA GCACCCACTA TGTGTCAGCC CTATGCTGTA 1370
|
