Tag | Content |
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EnhancerAtlas ID | HS052-18237 | Organism | Homo sapiens | Tissue/cell | Fibroblast_foreskin | Coordinate | chr19:5614730-5616140 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Foxd3 | MA0041.1 | chr19:5615367-5615379 | AAACAAACAAAC | - | 6.32 | Foxd3 | MA0041.1 | chr19:5615371-5615383 | AAACAAACAAAC | - | 6.32 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | CTTGTGATAT TTGAACAGCC TCACCAGAGA GCTCTACGCC AAAACACTAG AAGTGAAAAG 60 CTGGGAAAGC CCTAACAGAG CAAAGTTCCT CCTTTACATA CAAGGATGCT CACAGTCAGT 120 CCTTTTGGGG AGCAGGGTTG ATACTTGTCT TCACTGTACT TTACATCTTT TAATGTAACT 180 GCTTAACCTT GCTTAAAACA ACATTAACAG GCTAGGCGTG GTGACTCACC ACTATAATCC 240 CAGCACTTTG GGAGGCCGAG GCAGGCAGAT CACTTGAGGT CAGGAGTTCG AGACCAGCTC 300 AGCCAACATG ATGAAACCCT ATCTCTACCA AAAATATAAA AAATTAGTCA AGTGGCTGGG 360 CGCAGTGGCT CAAGCCTGTA ATCCCAGCAC TTTGGGAGGC CAAGGCGGGC AGATCACGAC 420 GTCAGGAGAT GGAGACCATC ATGGCCAACA TGGTGAAACC CCATCTCTAC TAAAAATATA 480 AAAAAATCAG CTGGGCGTGG TGGCGCATGC CTCTGGTCCC AGCTCCTCAG GAGGCTGAGG 540 CAGGAGAATT GCTTGAATCA GGGAGGCGGA GGTTGCAGTG AGCCATAATC TTGCCACTGC 600 ACTCCAGCCT GGGTGACTGA GAGAGACTCT GTCTCAAAAA CAAACAAACA AACAAAACAC 660 AACATTAGGA GGAATATCTA CATGATGAGA TTAGAAACCA TTTTTGAGCT GGGCACGGTG 720 GACCACACCT ATAATCCCAG CACTCTGGGA GGCTGAGGCG GGAGGATTGC TTGAGCTCAG 780 GGGTTCAAGA TCAACCTGGG TAACCTAGTG AGATCCCGCC TCTAAAAAAA AAAAAATTTT 840 TTTTTAATTA GCTGGGCGTG GTGGTTCACT GTGTAGTCTC AGTTATGCAG GGGGATTGCT 900 TGAACCTGGG AGGCTGAGGC TGCAGTGAAT TATGATGACC CCACTGCACT CCAGCCTGCA 960 CAACAGAGCA AGACCCTGTC TCTAAATAAA TAAACCATCT TTGCTTCTTA AAACTGTATT 1020 TTAAAAGGAA AAAACTAAAT GGGCACTGTG GCCTGTGCCA ATAAGCCCAG GTAGTCAGGA 1080 GGATCGCTGG AGCCCAAGAG TTCAAGACCG GCCTGGGTAA CAGTTGAGAC CTCATCTCAG 1140 AAAAGAAAAA TCTTTTATGT CAGAGCTTTC TATTTTATGA CTCACCACAT GCTTCGAATT 1200 ATAAAAACAC TCCCCAGTGC TACAGAAAAG CTATCTATGA GTAAATCCCT GAGCTACACA 1260 GCGTTTAAAT GGACATGGTT TAACACCAGG GTGTAGAAGC AGAACTGTGT GTTCATGGCG 1320 GTTTAGCTGT GTTCTCCCTC ACACGAGCAG CACGCGAGCA CCAGGTGCCT CGGGGCTATG 1380 GGCACATCCT GCCGTGTCTC CAAGTTACCT 1410
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