Tag | Content |
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EnhancerAtlas ID | HS048-00613 | Organism | Homo sapiens | Tissue/cell | Fetal_small_intestine | Coordinate | chr1:24338000-24338950 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
IRF1 | MA0050.2 | chr1:24338820-24338841 | TTCTTCTTTCTTTTTTTTTTT | + | 6.26 |
| | 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 |
GH01I024011 | chr1 | 24337999 | 24339230 |
| Enhancer Sequence | TGATCTGCCT GCCTTAGCCT CCCAAAATGC TGGGATTACA AGCATGAGCC ATCACGTCCA 60 GCCGATAATA ATTACATTTC AAAGGGTGGC AGCATTAAAC CCATCTATCA TCTTGAATTG 120 TCTCAAGACA AAGACTTTTA AATTATGTGA GAAGAGGACT GGTAGAATAC AGAGGTAAAA 180 GTAAGGTCTT CAGACTTAAA AGCTCTATCT AAATAAGATC TTTTGATGTG GGTCATTCAT 240 GAAACTAAAG CAAACAGATG AAGCCTACTA AGATCTTGAA GGTTTGGATT GTCAAAGAGC 300 CTGCCCCATT CAGCCGTGTC ATTCAGCACA GCCCGTGACT GTTCGGCCCC AAGGCAGTTG 360 ATGGTGCCTG ATCTACATGG GCAGGAGAGG TCTGCTAAAG CTCTTCAGCC TCTAGGAATG 420 GCCTTCCCCA CAGTGCCCTC CCCAGATGCA GCCATGGGGA ATAGCAAGCA AGGAGAATCC 480 TTCCAGAGAA CAAAACTAAG GGCTGTAGAT TGACCAGCCA AGGAACTCTA CTGCAGGGAT 540 AGCGAGTCCC CACTACTCCT GCCCTGCAGG ACTGTACAAG TGCGATGGAC CAGAGACAGC 600 TGAGTGTTTG CCATGTTCTT TTTTTCCCAA AGGGAGTTTT TATTGCACTT ATCCTGTTGG 660 GGAGAGATAA ATTGTCTTTA AGCTTACAGA TCTCTAGTCA TGAGAAGCCA CATCCTGACC 720 CTAATCCTCT AGAGATCCTG GACTTTGAGC TGGATTTAGT AACTGGATGT AACTTTATTG 780 CTGTATCCCT TGGGGAGGGC CAAATGCATT TCCTTTTTCT TTCTTCTTTC TTTTTTTTTT 840 TTTTTTTGAG ACGGAGTCTT GCTCTGTCTC CCAGGATGGA GTGCAGTGGT GCGATCTCAG 900 GTCACTACAA CCTCCACCTC CCGGTTCAAG TGATTCTCCT GCCTCAGCCT 950
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