Tag | Content |
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EnhancerAtlas ID | HS184-09358 | Organism | Homo sapiens | Tissue/cell | T47D | Coordinate | chr13:99302480-99303310 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Hnf4a | MA0114.3 | chr13:99302823-99302839 | GTTGGACTTTGTCCCA | - | 6.37 |
| | 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 |
GH13I098647 | chr13 | 99299411 | 99304639 |
| Enhancer Sequence | AGCGTCTAGT GTCAAGGCCA GGGGTGCTAC TAAACAGCCT CCAATGCACA GGGTAGCCCA 60 CATAGCCAAG AATTATGCAG CCCCAAGTGT CAATAGTGCC AAGGTTGAGA AACCATACTT 120 CAGAGATAAG AGAAGCAAAG ACAGGGTGGA GGCTTCTACC CTGGTCCCCT GGGGCAGGCC 180 ATTGTTTGCA AAGGGCACAG AGAGTGAGCA GGGGCAGGGG CTGGTCCTGC AGCTCTGCCC 240 CAGTGATGTC ATCGAGCCCT GGAACTCGGT GCCCTTCCTG GAAGGGCTTC GCCTAGATGG 300 AGACTGACCT GACAGGAATC GGCTCCACCT GTGGACGTAC GGAGTTGGAC TTTGTCCCAA 360 AACTGTGCCT GTGACATACA TTCCTACCTT CACAAGGCTC CTTCATGCCA ATCGCCCTGT 420 CTATAAAGCC TGTTTCTCAC TGCAGCAAGC TTCCTGCAAA GCCAGTTTCT CAAGCTTGCC 480 ATCCCGAGGG GTGTGGTGGC ATAGCTCGGA TGCTTCCGAG CCTCCTCTTC CTTGATTACA 540 TGAATTCCAA GACATGCAAG GATGTTCTAG ACAAGGAGGC CAAGCACTTG GTGAAGGGGA 600 AACTGACAGC AGCAAGGACT GAGAAGAGAA GCTTTGAGAA ATGATCATAA AATAGTCAGG 660 TTCTGATGAG GAAGTGCAAC TAGGATTGGC ACGAACTCCA TGCAAAGGAT GATGATGGTG 720 CAATGTTTTT GTGAGTTGAG TTCTGAGAGT TGGCTTGGAG CATTGAGAAG GGAAAGGTGA 780 AGAGAAAGGA ATTGGTCAGA AACACAGAAA TCAGAAAGGA AAGGGGTTCA 830
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