Tag | Content |
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EnhancerAtlas ID | HS180-27844 | Organism | Homo sapiens | Tissue/cell | Small_intestine | Coordinate | chr2:171590240-171590900 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Tcf12 | MA0521.1 | chr2:171590451-171590462 | AACAGCTGCTG | + | 6.32 |
| | 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 |
GH02I170733 | chr2 | 171589961 | 171591446 |
| Enhancer Sequence | AAAATAGTGG AGTGGAAGAA GCCACAAGGA AGAGAGGGAG AAAGACCAAG GAAGACTGAG 60 AAAAGGAAGA ACCAAGTTGG CCAGCCTAGT AAAGTGAGGG ATGACTCTTT AGATAGACCC 120 CACAGGGAGC TTCAGTTTAA AGGCTTACCC AAAGTCAGGG CTTTCTCCCT CCAGAGAGCT 180 GGAACTTTAG AGAAGAACCT GTCCCTGGCA GAACAGCTGC TGTAGTTCCA GTTCATAGGA 240 GTTTGCAGGG CATGATGAGC ATGTCTGTAT TGTAATGGGA AAGGACTTCA GACTCTTGGT 300 CTGCCAGCTA ATTGCATGAC TTCAGGCAAG TCATGTAACT CTGATTCCTT ATCTGAAAAC 360 TGAGGAAGGA GGACTGGATG ATCTCTTGAG GTCTTTTCCT GCTTGAAAAT GACATGATTC 420 TTATGAACGC TTGTGTATCT AACCAGGTGT TCTGGCTTAC CTATTGCTAA GTAGAACCAC 480 CCCAATACTT AATGGCATAA AATAGTAACC ATTGTACTAT GCTCATGTAC TCTGCAGGAC 540 AGGAATTCAC AAAGGGCACA GTGAGAGTGG GCTGTGTCCT ACAGTGTCTG GAGCCTCCTT 600 TAGGAATGAC TCCATTGGGG GTGACTTGAA TGCCTGGGAG CTAGAATCAT CTGGAGACTG 660
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