| Tag | Content |
|---|
EnhancerAtlas ID | HS118-13748 | Organism | Homo sapiens | Tissue/cell | Liver | Coordinate | chr3:195448750-195449990 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| IRF9 | MA0653.1 | chr3:195448876-195448891 | AACAAAAGTGAAACT | + | 6.15 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | AGCCGGGGGT GGTAGCAGGT GCCTGTAATC CCAGCTACTC GGGAGGCTGA GGCAGGAGAA 60
TTGCTTGAAC CTGGGAGGTG GAGTTTGCAG TGAGCTGAGA TCGCACCCTT GCGCTCTGGC 120
CTGGGCAACA AAAGTGAAAC TATGTTTCAA AAAAAAAAAA GCTGCAGTGG AGAGTCTGGA 180
GTTCCCATCC CCACCACTCA CAGCCTCCCC CATCATCAGC GTCCCCCACC AGAGTGGCAC 240
ATTTGATAGG ACTGAGGAAC CTACTTTGAT GCATCATTAT CATACATTGT ATTTTTAATC 300
CTCACAACGG CCCTGCAAGA TCGGCCCTGT TTTTACCACC CCCCACCTCC ACTGCTTTAA 360
GGGTGAGGCC ACTGTGCTTC TGGGCATCCA GTAACAACTC CTCGGAGCCA GAATCTGACT 420
CCTCACAGGC CTGAGCACTG CACCCCGTGG CCTCCTGCCT GTGCTCACCG TGGCCTGGTC 480
TGCGCTGCAC GTGTCCCGTT AGCTCCACCT TACAGGTGCG GAAATGCAGG CTTGGAGCTG 540
AGAGACTTGG CCAGGGTCAC AGGGCAGAGA GCAGATTCTC CAACTCAGGG TCCCAAGTCC 600
ACACGCTTTC CTCTCCACCA GATTTGAAGA TTGTACCAGG AGAGCCGCAG TGTTCCAGAG 660
CTACTGAGGG GCTGGGCTGG GATTTGCTGT ATTCGAGAAG ACCCCCTTGG ACCCGAGAGG 720
CTGTGGGCTT GGGGAGCATG AGGAGGTTTC ACAGCAGAAA GGACACCCCG GGGCTCCTGG 780
ATAAGCCAGA AAATGTGCCA GGGGAAGTCG GGCTCCAAGG GCACCACTCT GGGCTTCCAG 840
CTGTGTGGGC TGGACCAAGA AGGCTCAAAG AAATGATCTC AGGCTTGAAG TGGGGAGAAG 900
AAACTGTATT ATGAAGGCAG ACGAACAGTT CCTGCAAAAG TGAGATTTGT GTGTGCAGCT 960
GGGCCGCACT GGACCAGGGA TGAGAGTGGG TGCCCGGGAC TCGCCTATAC TGCCTGGGGG 1020
TGCAGCCCGC ACTCCTCACT ATAGTCAGAT CAACTATGCG TGCTTTCCAG TGGCCTGGGA 1080
GAGGACTCCA TAGGGAGGGA TGCTTACCTT GTGGGCTTTG GAATATAAGC CCTTTCACCT 1140
TCTCCGCTGG TCCTCATCAC GTTGGCAAGG CAGGTATTGT GACCCTGTTT TCTCAGGTGA 1200
GGACATGGAG GCTGGGAGGG GTCTAGAGAC TGGCCTGGCT 1240
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