| Tag | Content |
|---|
EnhancerAtlas ID | HS012-18390 |
Organism | Homo sapiens |
Tissue/cell | Caco-2 |
Coordinate | chr3:122083970-122084970 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| HNF4G | MA0484.1 | chr3:122084555-122084570 | TGAACTTTGCTCTCC | - | 6.3 |
|
| | 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 |
| GH03I122362 | chr3 | 122081592 | 122086178 |
|
Enhancer Sequence | CACTAACATG TGACAGCAGT TATAGAGGTC CAGCAACGAA GGTGCTTTTT TTGAGTTAAA 60
TATTCAGGTA AACTAGTGGG GATTTTTTGA CTGGCATCTG TCTATAAATG AAATATACTC 120
ACTAAAGTAT CTGACTATTA GTCACAACTT AAAGAAACTG ACTGAATGCA GGGTCAGAAG 180
AGATGGGTTA AAGTCCCAGT TCTACCACTT ACTAGCTTGT GGCTTTGGGG GTGTCAGTTA 240
GTATCTCAAG TATCTCTGAG TCTTTTTCCT CAGATAGAAA ATGAAGAGGT AGAGCTGTAC 300
CATCTCCAAG AGCTCTCTCT GATTCCATAA TCTTCATAGC AAACTTGAAA ATTGAAAAAA 360
AAAATTCACA TTTCCTTATT TGCTTATGTA CTACCCCATG GTTACCCCCA ACCCTATATG 420
TTATCAAGCT AGAAAGCAAA CCTCATGCAA CTCACTGATT GGTTTCTAAA CCCTCCTTGC 480
AGTGGTCATC CTGGTGATTC TATCTGGGCC CTAAAGACAC AAGGGCAGAT CTCAAGGCTG 540
AGCAAATTGT GTGTCACAAT CATTCCCAAA CACTCAGTAG AGTTTTGAAC TTTGCTCTCC 600
ACTAATGAGT CACTCTGTTG TTTGACTTGA TCTGCAAACA GTGACTTTTC AGTTTCCAAT 660
TTAACAGCCT TTGCCCTGCA GTTTCCTTTG TCAACACCTT CAAGGGCGTT GAAATACAAA 720
CTCCAAAATT ACTAGACTTT CACCAGTTTT ATATAAATTA TCTATATGCC GGCTGGACAC 780
GGTGGCTCAT GCCTGTAATC CCAGCACTTT GGGAAGCTGA GACGGGCAGA TCACAAGGTC 840
AGGAGTTCGA GACCAGTCTG GCCAACATGG TGAAACCCTG TCTCTACTAA AAATACAAAA 900
AAAAATTAGC TGGACGTGGT GGCAGGCACC TGTAACCCCA GCTACTAGGG AGGCTGAGGC 960
AGGAGAATCT CTTGAACCTG GGAGGCGGAA GTTTCAGTGA 1000
|
