Tag | Content |
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EnhancerAtlas ID | HS101-12748 |
Organism | Homo sapiens |
Tissue/cell | HT29 |
Coordinate | chr13:77511290-77512200 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOXC1 | MA0032.2 | chr13:77511659-77511670 | ATGTTTACATA | - | 6.32 |
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| 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 |
GH13I076936 | chr13 | 77511001 | 77512428 |
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Enhancer Sequence | GGATGCCCAG ATAGCTGGTA AAACATTATT TCTGAGTGTG TTTGTGGGGG TGTTTCTAGA 60 AGAGATGAGC ATTTGAATCA GTAGACTGAG CAAAGAAGAT CCGCCCTCAC CAATGTGGGA 120 GGGCATCATC CAAGCCATTG AGGGCCTAAA TAGAACAAAA TGTCAAAGGA AGAGCAAATT 180 TGCTCTCTTC CTTCTTGAGC TGGCACTTGC ATCTTCTCCT GCCCTAGGAT GTTGGAGCTT 240 CTGCTTTTCA GGCCTTCAGA CTTGGACTGA ATTACACCAT CTTTTAGTTC TCCAACTTAC 300 ATATGGCAGA TTGTGGGACT TCTTGGCCTC CATAATCATG TGAGCCAATC CCCATAATAA 360 ATCTCTTATA TGTTTACATA TATCCTATTA GTTCTATTTC TCTGGAGAAC CATGACTAAT 420 ACACCCTCCC ACTGCTTCAT TCCAGTTCCA CATTTGGCAA GCAACATTCC ATGACTCATC 480 TGGCTTCCCA GCCATGTTGC TATAGGGAAG GACCCCAGAT AATGAAAGAA ACTAGCCTTG 540 CAATATAAAG GAACTAAAAT GATACGTTGG CATTCTGATC TATGCATCAG ACTCTCACCA 600 GTTTGTTAGT GAGACTGTCA TTTCCCCGGT GGCAGATTGC CTGTAAATCC TCAGTACTAA 660 AGCTGGATCC AGCCATGGAC ATGCAGCTGA CGACATGAAG GCATTTTCCC AAGAAGGCCA 720 CCTGGCCTCT CTAAACTCCC CCTCATTACT CCCTGATAGC AACTGGTCCC ACCCCAGGTT 780 TCATCCTATC CTAAGGTGAG TGCCTGAGCT GAAACTGGTC CCTAAAATTC CAGAAGTCTT 840 TGGAGACAGG GCAATTCTAA ACCCTTCAGG GAAGTCCCTG TTGTCCAATT TAGGACATGC 900 AAGCAGAATG 910
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