| Tag | Content |
|---|
EnhancerAtlas ID | HS012-06662 |
Organism | Homo sapiens |
Tissue/cell | Caco-2 |
Coordinate | chr11:118996330-118996990 |
Target genes | | Number: 20 | Name | Ensembl ID |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| MEF2C | MA0497.1 | chr11:118996759-118996774 | AGGTTAAAAATAGCA | + | 6.28 | | NR2F1 | MA0017.2 | chr11:118996720-118996733 | CAGTTGACCTCTG | - | 6.15 | | Nr2f6(var.2) | MA0728.1 | chr11:118996724-118996739 | TGACCTCTGGAACTT | - | 6.04 | | TP53 | MA0106.3 | chr11:118996405-118996423 | TACATGCCTAAGCATGCC | - | 6.3 | | TP53 | MA0106.3 | chr11:118996405-118996423 | TACATGCCTAAGCATGCC | + | 6.61 |
|
| | 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 |
| GH11I119125 | chr11 | 118995918 | 118997893 |
|
Enhancer Sequence | TGAGCTGTGA TTGTGCCACT GTACTCCAGC CTGGGTGACA GGGTGAGACT CTGTCTCAAG 60
AAAAAAAATA TTTATTACAT GCCTAAGCAT GCCTAGCAGT GTATAGACAC CCAAGGTGCA 120
GTATAAACTA CACAGATACG GCTTTTTATG TTCAAATGGA ATCTACATTT TAACAGAAGG 180
TATTAGCAGA GTGGTGGAGT AAACCGTTGG ATAGGTTAGG TAAAGGCAGA TTGTATGGCA 240
CTGTGAAAGT CTGGCAGGGG ACTTATGATT CAATAAGAAA TAAGGAGCTT CTAGGCTCAT 300
CTGTAGGCTC TATGGAGTAG AACCGTATAT GGACTAGAGT CAGCCCAACA TGACCCTACC 360
ATTACCACTA GTGTGTGGCC GTGAGCAAGT CAGTTGACCT CTGGAACTTC AGGTGTTTAT 420
CTATAAATGA GGTTAAAAAT AGCACCTACC AGCTGGGCGT GGTGGCTCAC ACCTATGATC 480
CCAGCACTTT GGGAAGCCAA GGTGGGTGGA TCACCTGAGG GCAGGAGTTT GAGACCAGCC 540
TGACCAACAT GGGGAAGAAA CCCTGTCTCT ACGAAAAATA TAAAAATTAG CCAGGCGTGG 600
TGGCGGGCGC CTGTAATCCC AGCTACTCAA GAGGCTGAGG CAGGAGAATC GCTTGAACCC 660
|
