| Tag | Content |
|---|
EnhancerAtlas ID | HS101-10036 |
Organism | Homo sapiens |
Tissue/cell | HT29 |
Coordinate | chr12:31370130-31371160 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NR2F1 | MA0017.2 | chr12:31370976-31370989 | CCCTTGACCTCTG | - | 7.34 | | RARA(var.2) | MA0730.1 | chr12:31370440-31370457 | AGGTCACTAACAGGTCA | + | 6.57 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_63350 | chr12:31368050-31392738 | NCI-H69 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | AAAAATACTT CACAAGAAGA TCATCCCTAA GACACATGGT CGTCGACTCT CCAAGGTCAA 60
AATAATCTGT ACAATGCGTC CTTCACTTTC TTCCTTTCCT CCCCACCCCT CACTGTTCAA 120
CAGATAACCT GAGTGCATTC AGTTTGTAAA GCACAGTGCT GGGGCCGTGA AAGCCAGAGA 180
CGAATCAGAC AACACACAAC CACTCTCAAA GAGATTCAGG GATCCCAGGA GGGAAGAAAG 240
GAACATCAGT AAGCACAACG CCCCGCAAGC CTGGGTTTCA CATCTGTTTA GCAGCAGCAT 300
GACCTTAAGG AGGTCACTAA CAGGTCAACG CCTCAGCTTC TTCCACTGAA AAACAGGAAT 360
GGTCACTTCT GCGTCACTGA ATTACCTCTC ACTGAATTAC CTCGAAGGTG AAAAGGAGCT 420
GGTGATGTCT GGTGCTCCTG TCCTGGCTGA CACAGCTAGG TCCTCAGCAT TGGCTATTAT 480
TGCCTGCAAG ACGGGGAGTA GTGAGGGGCT TCAGGCACTC AGGAAACCCA GAACTCCCAC 540
AAGTGGGCAG GGCAAAGTAG GCAAAATTTC AGGGAGGAGG CGGTCTAGAG CAGATCACGG 600
AGAGGGAAGC TCCAGGCTTA GGAGACAGAC ACTCTGCAAG AGAACACCGC GGAGGACGAA 660
ACAGCAGAGC AACAGCAAGC AGCGCCTCTG GCTGGAGCTG TGCCTTTCAA GGAGCCGCAG 720
TAGGAACCAC GCTCCTCTTG GGGTGGCAGA GGGATGGGCA GGACCATGCT TGGGCTCCCT 780
GTTCCACCGC CTCCAAAGAC GACATCCCCA TTCCCCATGA GAATGTTTCC TATGAAGCCA 840
GGCTGGCCCT TGACCTCTGC AGGGCTGCCA CTGGCCCTGG CCCATCATCA TGCCAGTCCC 900
TAGAGGCTGA TGGTGAGAAG GGAGCAGAAA GCGCCCACTC CTGACCCAGA TTCGCTGCTT 960
CTCCTCCCCT GCCTCTGTCA TGACCCCAGG GAAGCAAACC CTGAACCGGG GCTCTCGCCT 1020
TCACCTTTAC 1030
|
