| Tag | Content |
|---|
EnhancerAtlas ID | HS118-14655 |
Organism | Homo sapiens |
Tissue/cell | Liver |
Coordinate | chr4:185587320-185588610 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| IRF1 | MA0050.2 | chr4:185587978-185587999 | AGTCTGAAAGTGAAACCAGAT | - | 6.71 | | IRF2 | MA0051.1 | chr4:185587982-185588000 | TGAAAGTGAAACCAGATT | + | 6.66 | | LHX6 | MA0658.1 | chr4:185587462-185587472 | ACTAATTAGC | + | 6.02 | | PRDM1 | MA0508.2 | chr4:185588460-185588470 | GTGAAAGTGA | - | 6.02 | | STAT1 | MA0137.3 | chr4:185587802-185587813 | TTTCCTGGAAA | - | 6.62 | | Stat4 | MA0518.1 | chr4:185587799-185587813 | CAGTTTCCTGGAAA | - | 6.5 | | Zfx | MA0146.2 | chr4:185588008-185588022 | CAGGCCTGGGCCCA | - | 6.06 |
|
| | 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 |
| GH04I184666 | chr4 | 185587456 | 185588699 |
|
Enhancer Sequence | AACTTATCCT AAAAAATGCG ATGTAGGCTG AGTGCAGTGG CTCACACCTG CAATTCTAGC 60
ACTTGGGGAG GCCATGGTGG GCGGCTCACT TGAGGCTAGG AGTTTGAGAC CAGCCTGGCC 120
AAGCTGGCAA AACCCTGTCT CTACTAATTA GCCGGGCATG GTGGTGCATG CCTGTAGTCC 180
CAGCTACTCG GGATGCTGAG GCACAAGGAT TGCTTGAACC CAGGAGGCAG AGGTTGCAGT 240
AAGCCAGGAT CACACCACTG CACTCCAGCC TAGGCAACAG AGTGAGACCC TGTCTCAAAA 300
AAAATAATGG CAATGTGTTT CTTCATGTTT TCAAGATGTT CCCTTAGCTT TGGACCTGTC 360
TTTCTGTTCT AGACACATCA ACCTATTCAG GACATCTTTG GCATTTGCAT CTCTAATCCT 420
AGATACTGGG ATGGCCATCC ATGTCCAGAT AGTGGTTTCT GCTCCAACAT GATTTATTTC 480
AGTTTCCTGG AAAGTGCATG AGAGGCCTTT CCATTTCAAG CCTTATCTGC AATCTCATTT 540
CTGGATTTCT GACCTTTGCT TCGGCCTTGC TTTGGGGCTT CGGTCCCAGG TCGTATCAAA 600
GATGGCTTGT TTATTGTTCC AGGCAGAGCT TCAGGGTTGG GATAATTCTA GATGTACGAG 660
TCTGAAAGTG AAACCAGATT ATTTATCTCA GGCCTGGGCC CAGGTGTAAA ACAAAGTCAG 720
TCCAAAGGAG AAACACATAG TTAGAATGGG AACACCATAT GAAGGTCTGA ATAAAAGCCA 780
AATCCTGAGT GCTTATCAAA GCAGGGGTGG GACAAGAGTC CAAACAGCAG ATGATTGACT 840
GAAGCTCAGG TAACAGGTAA TTCAGTTCAG AGCTGCTAGC GTCTTAGAGT TTCACGGCCA 900
CCTAGAGTAA AAGGCGTGGA CATGGTCACT AAAGCACTGG CATGAAAGCC AGGAACCTGA 960
TTTCTGGATT AGGGGAAGGT GGCCACAGAG ACCCAGCATG CTGTTTTCAC AAGGCTCTCG 1020
TCACCTGCCT GTTTCCTGGT AGCTCAGCTG GACGTTCCTT CTCAGTCTCT CTCCCTCATC 1080
CTGTGAGAAA CACAGTCACC CATCCAAACC CAAAGAATGG ACTTAGAGGC ATGGAGAACA 1140
GTGAAAGTGA GACTTTTTTT TTGAGACAGA GTCTCGCTCT GTCGCCCAGG CTGGAGTGCA 1200
GTGGCACGTT CTTGGCTCAC TGCAACCTCC GCCTCCCGGG TTCAAGCGAT TCTCCTGCCT 1260
CAGCCTCCCG AGTAGCTGAG ACTACAGGCG 1290
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