| Tag | Content |
|---|
EnhancerAtlas ID | HS059-47262 | Organism | Homo sapiens | Tissue/cell | GM12878 | Coordinate | chr9:79370160-79371560 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| IRF1 | MA0050.2 | chr9:79371005-79371026 | ACTAAGAAAGTGAAAGTAGAT | - | 6.92 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr9 | 79370404 | 79370500 | | chr9 | 79370861 | 79371400 |
| | | Number: 1 | ID | Chromosome | Start | End |
| GH09I076755 | chr9 | 79370194 | 79371495 |
| Enhancer Sequence | ACGTTCACAC CATATCTTTG ATACCTAAAG CACTGGCTCA TTCACGGTAG ATGGATACTT 60
ACTGAATGAG TGAAGAAATA AACAAATGAG TAAACGAATG AAAAAAAGAT AAACCGATGG 120
AGAGAGAGAA TGAGGGAGGG AGGAATGGAT GGCTGGATGG GTGGTTAAGT GAACACCATG 180
TGCCACTCTG GGGATATAAA AAAAAATACT CAGCTTCCTG CCCTAAAGAA TTTGTGGCTA 240
AGCATTCAAG AAGCTACACT GTCTAGTGGG GGTGTGGACA AAGAACGCTG GGAGGAGAGG 300
GCAGGAATCT AGAAGCCTGC CTTGAGGAGT CAGGGAAGGC ATTCAAGGGG CAAGAAGGGG 360
TCTTATTAAA ATGCAGATTC TGATTCAGAT ACCTCGGGGA GAATCTGGAT TTCTCACAAG 420
CTTCCAGGTA ACGCTCAATC TGCTGCTGAC CATACTTTGT TTTTGTTTCT GTTTTGAGTC 480
AGGGTCTCAC TTTGTCACCC CAGGCTGGAG TGCAGTGACG CAATCTCGGC TCACTGCAGG 540
TCGACTTCCC TAGTTCAAAC GATTGTCTCG CTTCAGCCCG CCAAGTAGCT GAGACCACAG 600
GTGCACGCCA CCACGCCCCG GTAAATTTTT GCATTTTTAG TAGAGACAAG GTTTTGCCAT 660
GTTGTCCAGG CTGATCTTGA ACTCCTGAGC TTAAGTGATC CACCTGCCTC GGCCTCCCAA 720
AGTGCTGGGA CTATAGGCGT GAGCCACCGC GCCTGGCCAG GGGATCATAC TTTGAGGAGC 780
GAAACTTTCA AATAATTTCC TGGTGGTCCT TCCCTTTCAC CTCCTACCAA CCACCAGCTT 840
TGGCTACTAA GAAAGTGAAA GTAGATGAAA AATATTTAAA ATTAACAAAC CTCAGCTCTT 900
CACAGAGCCA TTTTGATGAA TATCTGAAAA TCCCCCAACT AATGAGAGGT CATGTAAGTG 960
CATATGTCAA AAGGAACTGC TTTTTTAAGA TAAAAAATTA CTCTTGATTT AATGTATTCC 1020
ACATTTATCA GTGACTTACC CTAACGTCTC TTCTAATCTG CATGAAAACG TCTCTGTATA 1080
TCCTGGATCA CTTACGGCAC CCAGGAACTG TGAAGCTGGC CTAAACCAGT CCCTGGCAGC 1140
TCTCCTCTTT GAATTGGTAA ACCCCTGGGA GCTGCCTGTA TGGCTCACTG GCCAGATGGC 1200
GCTGCTTCCC CATTCTTTCC AGAGTTGCAT GGCTGTCGCA ACTAGGAACC AGGCGCTGGC 1260
TTTCCATCCT AACATTTGAA TGCTTCCTCC ATCAGAACAG CTGCATTCTC TTTGCCAACA 1320
CATGTGTTTT TCAAAATCTC ATTAGACATC TAACATTTTC AGCCAGATTG TGTCCTGAAG 1380
GCACTGTGGC CTCCCAGGAG 1400
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