| Tag | Content |
|---|
EnhancerAtlas ID | HS034-13639 |
Organism | Homo sapiens |
Tissue/cell | ECC-1 |
Coordinate | chr18:21402340-21403660 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| HNF4G | MA0484.1 | chr18:21403556-21403571 | AGGGAGCAAAGGCCA | + | 6.35 | | JUN | MA0488.1 | chr18:21403073-21403086 | GAAATGATGTCAT | + | 6.59 | | JUND(var.2) | MA0492.1 | chr18:21403072-21403087 | AGAAATGATGTCATT | + | 6.65 | | ONECUT1 | MA0679.1 | chr18:21402556-21402570 | TAAAAATCGATATA | + | 6.35 | | ONECUT2 | MA0756.1 | chr18:21402556-21402570 | TAAAAATCGATATA | + | 6.54 | | ONECUT3 | MA0757.1 | chr18:21402556-21402570 | TAAAAATCGATATA | + | 6.17 |
|
| | 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 |
| GH18I023822 | chr18 | 21402241 | 21403253 |
|
Enhancer Sequence | TAAGGCACGT AGGTAAAATG TCAAGCCTCT TTTCAATTAA GAAATAAATA GTGAAACACT 60
TTCTCTGATT TTCACAAAGT TGATCACCCT TAGAAAATGT CAAGCCTGGC TCATGGTCTG 120
GTTAGACGGT TCTCTAGGAG CCCTGTCGTT TGTTACCTTG CATTCTCTAA ACAATCACTT 180
AAGTTTTGCT ACTGAATTTG TCCTTAACTG TCATTTTAAA AATCGATATA ACAACCTATG 240
TACCTTGGCT GAACCCCATG GGTTATGATG TCTTCACTGA GCAGAGCTCA TTTATAACTC 300
ATTCACAGTG ACGAGGGTGT CACTTTTTTG GTGTTATTTG AGAGATTTTG GCCCGCTGCC 360
CTAAATTCTT CCATTGTTTC AAACCAACCA AATAGTCAGA GGAGAAATGG GTGAGGATGG 420
GAATTTTTCC TATGAATGCT GTAAAGCATG AAGCCCAAAT GAGTTCCAGG AGGGAGCTGC 480
AAACCTGACT CAGGGATGAG GAATTCCTGA GGGCAGAGGG ACAAGAGAAG AGAGCACAGC 540
CTCGCCACAG GCAGAGAGAA GGCCCGCAGG TCTGTTCTTC AAGGTATTAG GGCTTCTACC 600
TGTCCTGGAA ACAGATTCCA AGAAGCATTT GGAATTTTAC AAGGACACAA AATGGCACCA 660
ATGGAAATCT AATTTAGGAT CAAAATGTAC GCCATCTTTG TTAAGCATCC ACGGTTCATT 720
CAGAATGGGG GAAGAAATGA TGTCATTTCC GAGTTGTGTC AACCCAACTT GCGTGGCTGG 780
AGGTTGATTA ACCCATTGAA TGAACTAGCA GGCTTACTTC ATCATTCACA GAGTAATTTA 840
GCACCCATTG CCTCACATCA TAAGAACTTG GCAAACTGAG GAGAGTTGAA GAGAAAACAG 900
AGCTGAGAGG TTTAGTAAAT TGCCAGCCAC AGCTGGATGT TTGTAGACAA AGTCTTCAGA 960
TTCCAAACTC TTAACAGGCC CCTCTGCCTC CTGCGTGACA ATAACAGCAG CAGTTTGTTC 1020
TCTGTTAACT CAAATAGTTG GAATACATTT TGCTTCGTTT CCTTGTCCTC CGGGACACCT 1080
TTCCCCTAAG TCTGAGTTGG GAGCCCTAGT TATGTTATGT CCCATGGTAA CTGGTGCCTC 1140
CTCCCAAATA CCACTGTCCA AACTGTACCA CATTTTCCTG TCTTCTAGTC CTTATTCCTC 1200
TCTGGTCCTC ACCAGCAGGG AGCAAAGGCC ATGCTTACTG TGTTTACTGC CTTGTCACCA 1260
GAACTTAGTT CCAAGCCTGG CACATAGTAG GCCCCCATCA ATGTATGTAG AACAAGAGTG 1320
|
