| Tag | Content |
|---|
EnhancerAtlas ID | HS052-01212 | Organism | Homo sapiens | Tissue/cell | Fibroblast_foreskin | Coordinate | chr1:45731310-45732500 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| IRF1 | MA0050.2 | chr1:45732031-45732052 | ACTCTCTTTCTCTTTCTCTTG | + | 6.45 |
| | | 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 |
| GH01I045265 | chr1 | 45731121 | 45733448 |
| Enhancer Sequence | AACACTCTGG AATTGAGTCT GGGAGATTTC TGCCTCAGTC TACCTGTCTA TCCTTTTATT 60
TTGGTTTATT TATTTATTTT TGAGATTTGG TCTTGCTCTG TCACCCAGGC TGGAGTGCAG 120
TGGCATGATC ACAGCTCACT GCAGCCTCGA TCCCCTGGGC TCCAGCAATT TTCCCACATC 180
AGCCTCCTGA GTAGCTGGGA CCACAGGTGT ATGCCACCAC GCCCAGCTAA TTTTTGTATT 240
TTTTGTAGAG ACAGGGATCT CACCATGTTG TCCAGGCTGG TCTCTAACTC CTGGGCTCAA 300
GTGATCTGCC TGCCTCAGCC TTCTAAAGTG CTGGGATTAC AGGTGTGAGC CACCACGTCT 360
GGCCTAGAGG CTTTTTTTTT TTTTTAAGCC AGTGGATTAG GATACAGAGA ACACTAGTGT 420
CAAGTTCACA ACTACGCCAA TTGTCATGCT GGGGTATGAG GGGAGTGGGT GGATGAGCAG 480
AAAGAACACC CAGGGGGGCC ATAAGCAGGT GAAAGATGAT TTTATTCAGC AGCAGCTCTC 540
ATCAACAGCT CTCTCACACT GTCCGCCCTG TCTTGGCTGC TTAGTCCGGC GGCTCCCACA 600
CACAGCTGCG TGGCTGGCTC TCCCTTGCCT TCAGGGTCAG CAGCTAAACT CTCTCTGGGC 660
ACAAGCAAGC CAAGCTGTGT CCTGGCTCCC CTCTGTCTGT CTGCAAAGAT GGACAGCTTT 720
GACTCTCTTT CTCTTTCTCT TGGCTCCAGC ATGCCTGTAC AGTGTTATCA GGGCAATTAT 780
ACCTTTTACA GACAATAGTG GCTTAGAGTC AAGGAATGGC CTTCCCATGT TATGGCTACA 840
TGGCTGTGAT AACAAGTGGA GTTATACGCC TGCACTCTAA ACTCGCTGAG TCACTCTGGA 900
TGTTTACCTT GGCCTATTTT TGACCAAAGC ACAGCCGTAT TCCTTACAGT TAGTAATGAG 960
AAAGAATGAA GGAGAGAGAA AGAGTGAGAG CTGGCAAGAG GGCTTCCTAA GTTCTCTTTA 1020
GCACTGCAAT CCTTGGCTCC AGGTTATTCC TGAGGTTCTA CCACTTCCTA GCCCTGGAGT 1080
TTCATGAGAT GACCTGTATC CTTATATAAA TTCATTTTTC TTTTGCTTAA ATCTAGTATA 1140
ATTCTGTTGC ATGCAAACCA CAGTCCTAAT GGCACTAGAA AACAATAAAA 1190
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