Tag | Content |
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EnhancerAtlas ID | HS048-02470 |
Organism | Homo sapiens |
Tissue/cell | Fetal_small_intestine |
Coordinate | chr1:156349230-156350330 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
IRF1 | MA0050.2 | chr1:156349887-156349908 | CTTTCCTTTCTTTTTCTTTTT | + | 6.8 | Klf1 | MA0493.1 | chr1:156349538-156349549 | AGCCACACCCA | + | 6.14 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr1 | 156349251 | 156349348 | chr1 | 156349409 | 156349576 |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I156378 | chr1 | 156348182 | 156349873 |
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Enhancer Sequence | AAACAGAGAG GCTGGCTTAG GATTGCTCAG CACTGCTGGG TCAGAGTACA AAGAACCCCA 60 GGCCAGCTGA GGCCTCCTTG CCCTTTGAGA CCCAGATAAG TTTGCCTTGA ATTCCAAAGG 120 CTTCCCCAAG TTTTCCAGGC ATTCCCAGGA GACTTACATT CTCAGCTGTC TGCCTCCCAG 180 CTCCTGGATT TTAGTGTCAC CCAGACAGGA ATGAGGCCCC TTCCTGGATT CTCCCACAAA 240 CGCTCCACCT ACAGGATGCA AATGTGAGTG TGGGAGATTT TACTCCAGAT TGCCGGGCTG 300 CTGGGAGAAG CCACACCCAA CAGACTACTC AGGACACGGT GGTCCCTAAG CCTCCCACCT 360 TGCTGGCTTA CACCACAGGG TCCCCAGCCT TCTCCTTCAC CTTGTTGTTT GGGTCCTTCT 420 GTCTCTCCCT CCAGGATGGA CCTGGGAACC TCATGCAGGA AGGCAGGGTA AATGGGCTTC 480 CAGTTCTTTC CCAAAATGCA CAGGCCCAGC CCATTCAGTA CTCAGCAAAC AGAGGCCTCT 540 CCCAAACACT GAAGGGTCCA CCCTCTCTAG GAGAGATTGA GGTTATCATT GTTTTCCTGA 600 TATGTGTATC AAGTACCCAG CATAGTCCCT GACATGCAGT GGCCTTTGCC TTTTTTCCTT 660 TCCTTTCTTT TTCTTTTTTT TTTTTTTTTG AGATGGAGTC TTGCTCTGTC TCCCAGGCTG 720 GAGTGCAGTG GCATGATCTT GGCTCACTGC AACCTCCACC TCCCAGGTTC AAGCAATTCT 780 CCTGCCTCAG CCTCCTGAGG AGCTGGGATT ACAGGAGTGT GCCACCATGC CTGGCTAATT 840 TTAGTAGAGA CAGGTTTTCA CCATGTTGGT TAGGCTGGTC TCGAACCCCG AACCTTGTGA 900 TCCGCCTGCC TCGAGCCTCC CAAAGTGCTG GGATTATAGG CATGACCCAC TGTGCCCGGC 960 CTTCTTTACC TTTTTTGATA CTTAAAAAAT GCCAGTGTTC TGGCCGGATG CAGTGGCTCA 1020 CACCTGTAAT CTCAGCACTT TGGGAGGCTG AGGTGGGCGG ATCACCTAAG GTCAGGAGTT 1080 CGAGACCAAA CTGGCCAACA 1100
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