| Tag | Content |
|---|
EnhancerAtlas ID | HS118-13463 | Organism | Homo sapiens | Tissue/cell | Liver | Coordinate | chr3:160340070-160341170 | 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 | chr3:160340326-160340347 | TCTTTCTTTCTTTTTTTTTTT | + | 6.25 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | CATTATCAGT ATCATGAGAA TTAAATGAGA TAATATATAT GGAAAAGCAC AGCACACCCA 60
GGTGTCCTAA ATACCTTCAT TTTAAAAATT CCAAGCCTAC TAAAGAAAGC TGTAAGCCAG 120
ACACATAGCA AGTTTAAAAA GATGTTTGTT TTACCTTCCT AGGGCAGGGG ATGGTGTGAG 180
TTCCCAGACA GAACATGACA GCAGAGCCCA GGTTGAGCAA GAGAGGGTGG GAAACAGAAA 240
TGTTTCCAGC AATTTTTCTT TCTTTCTTTT TTTTTTTTTT TTTTAATCAT GAAGATTCAG 300
TGTGTCCTAC AAGTGAATGT TTGAGTCATT CTGAATTAAA CTGGGAGAAT ATGATGATTA 360
TCTCTAGTTT GGTGTGCCTA ATCTATCTTT TCTTTTGGGG AACTCCTACT GCATTCCCTT 420
GGCTCTTGAC GGTTGTCAGT TACAGCACTC CATTTCACTC CTCTCTTTCC CCTCAGAGAA 480
CAGAGATGAC CACATGACCA GGAATGTTAG TAAACATTTT CTCCTCTACG TGGATGAAAA 540
CCTGCCTTCA GTAGAAGAGA TTGAGACAGG CAGCTGTGAG AGAGAGCATG AGGACATTGC 600
CTGAGTTCCT GGATTCATCT GTCCCTGAAG CTGGACTATG CCCCAGACTT CCAAGCTGAA 660
AAAACCAGTA TAGTCCTGAG CTTTCATTGC TTATACTTAT TCAAGTTGGG TTTCTGTAGC 720
TCAAAGTGTC CTGGCTAATA TAGGAACTTC TGCAAAATGC ACAAACTTGG CCTCCAAGTC 780
TGGAGTTTCT GATGTGGTAG GTATGAAATG TAGCTGAAGC ATGTGCATTC TTTTTAAGCT 840
TCTCTAAGCT CTATATCCTG GCTCAAATTG AGAACCATTG CTTTTTTTTT TTTTTTTTTT 900
TTTCTTTTTG GATTTCAAAT TCACAGGACA AATTTGGTCA TATTCAGTTC ATGGTATGTT 960
ATCATTATTG GTTCATGCAA TGTCAACATT CCTCTCTTAT TTTGCTAACT ATATTTTATT 1020
GCCATACTCC ACCTCCCTGA AGACCACAAT TCTAGTATAT TTAATGAATA ACTTTTTTAT 1080
GTGTTTTTGT AAAATATGTT 1100
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