Tag | Content |
---|
EnhancerAtlas ID | HS101-32187 |
Organism | Homo sapiens |
Tissue/cell | HT29 |
Coordinate | chr4:24644050-24645380 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
IRF1 | MA0050.2 | chr4:24645342-24645363 | AAAGTAAAAATAAAAGTCAGA | - | 6.2 | JUND(var.2) | MA0492.1 | chr4:24644628-24644643 | TGAGGTGATGTCATA | + | 6.11 | NFE2L1 | MA0089.2 | chr4:24644777-24644792 | TAATGACTCATCAGT | + | 6 | ZNF263 | MA0528.1 | chr4:24644434-24644455 | TTCTCTCCTCTTGCCTCCCCC | - | 6.01 |
|
| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr4 | 24644599 | 24645216 | chr4 | 24644640 | 24645193 |
|
| Number: 1 | ID | Chromosome | Start | End |
GH04I024642 | chr4 | 24644141 | 24646013 |
|
Enhancer Sequence | ACTCTGCCTC AAAAAAAAAA GATTCCAATG GGTGCACAGC TAGCTCCAAG AGTGTGGAGG 60 GACTCTTCTC AGTTGTGAGA TCATGAACCC AAATTTCAAG GTCCCAAAGT TTTGTTGTAG 120 TGTGGATGGC CTGCCTTCTA CTTTACACAG GGTTCTCGTA AGCCTTTCTC TGAATTGTAT 180 TTTTTACCAA AAACTTCCCT ACAAACAACT CTCAGGACAG CCAATTGTTA AATTGTCAGG 240 AAGTTTGCAA GCTGGTTGAC TTCATGAGGA TAGCTTGAAC TTGGTCATAG CAGACTATTT 300 ATGGTATAAA TTAGCACCCC TGTCCCAGAG CTGGATGTTA GGCACTTACC AGCACACCAC 360 TGTTCATGTC TTTATGATTT TATTTTCTCT CCTCTTGCCT CCCCCACCAC CTGTCTAAAT 420 TTAATTCAGA ATCACTATTT CCACTTGTGG TAGAAACATA GAACATTTGC ATTTGAAAAT 480 ATAAAATGGT CAAGAGCAAG TGGTCTCATC TTTCTAAGTT TTCGTCTCCT GTCCGTAAAG 540 TGGTGATAGC AACATCTTCC TCATAGGTTG TGGTGGGATG AGGTGATGTC ATATACATCT 600 GGTCTCAGCA AATACTCAAT ACTCTCTGGC CATATCACTG GTCTCATTCT CTGCATGCAC 660 CCAGCCTTGG GTTACTTATT TATCAACCGA CACGTTTTGG AGCTCGCATT CTTTGAATAG 720 CTGACACTAA TGACTCATCA GTGAAGTGTG TTTTCAGTAG GAAAATGCTC ACAACAATCA 780 GTGCACACTC TTCTACATCT GTGATGAACT ATGAAAACCA GGTCTCTTTC TGCAAAGCTA 840 TACCCTGAGA AGTCAGAGAG TATTCTGAAT TAAATTCTTA CACTGTTATC CATGCTGGAC 900 TTATTTTACT TGGCCAAAGT TATTCTTCTG AGAGCACCCA CCTGGCATTT ATCTCTATTC 960 AACTTTGCCT TAGTTATGTA GGACCAGCTT TCCTATGTGT TGAGGTCATT GTGCATTGAG 1020 GTCAGTCATG AATAGGCTGG GCAACAGCCC TTATCTCCCC TTCTCCAGAG TCTGAAACAG 1080 TGCATTCCCT CCTATGCATC ATCTGACATG GATAAAGGCT GTTAATGTGT TTTGCCCAAT 1140 GGAATTCATA TCTGATTCTC TCTGCAACAG TGATTTTACT TGGAAAAAGA AATATTTTCC 1200 TATACTAGTG CTACTATATT TGATGAGATT AATTGCCCTC TACTTTAAAA TATGCATATT 1260 TTAATGGCTA ACAAAGATCT CAAGAAATAC ATAAAGTAAA AATAAAAGTC AGAAAAAAAT 1320 AGAGGTTATT 1330
|