Tag | Content |
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EnhancerAtlas ID | HS145-21763 |
Organism | Homo sapiens |
Tissue/cell | NHBE |
Coordinate | chr5:178069320-178070020 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
GSC | MA0648.1 | chr5:178069575-178069585 | GCTAATCCCC | + | 6.02 | Stat6 | MA0520.1 | chr5:178069835-178069850 | TTTTTCCTGAGAACT | + | 7.26 | TFAP2C | MA0524.2 | chr5:178069693-178069705 | TGCCCCAGGGCA | - | 6.44 | TFAP2C | MA0524.2 | chr5:178069693-178069705 | TGCCCCAGGGCA | + | 7.22 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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| Number: 1 | ID | Chromosome | Start | End |
GH05I178641 | chr5 | 178068881 | 178070273 |
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Enhancer Sequence | ACAGCAGAGG GCTCCCGTAT CAATAAACTC GCCCTCCCAG GCTTCTGTTG CACAGCTCTC 60 AATGAGCACC TTTGGGATCC AGCCCATGTT TCCTCTTTCA GCTCCTGCCA GTGCTGTGAA 120 GCAAGTTCAC TGTGCTCTAG TTACCACACT GTCTGAATCT GGTAAGACAG AACACCCACA 180 TATAAATTAC ATGAAGAGGG TTTGTTACTT ACTCATAGGA AGCAAGGGAC AACGGAAGCC 240 CAGGATTCAT TGGAAGCTAA TCCCCAGGGC TCAGGAAAGC CCCCTGAGGT TGGATTGGAG 300 TCTTGCTGTG GTGTGTATGC TCCACTTGGA CTGCAGCCAA AGGGCCATGG AAGAAAGTGC 360 AACCTGGGTT TTATGCCCCA GGGCAACATG ACTCACTGGA ATAAGGCATT GAAGGACATC 420 CTGTTTCTGG GGTAGGGGGG ACTGGAACAG AGCCCAGGCC TTTCCAGCCA GCTTCTCCTT 480 ATCTCACATT GTTGTGTTCC CAGCACATTC TATGGTTTTT CCTGAGAACT GCAAGTAAGA 540 AAGAGGAGAG AACTGGGTTG GTCCAAGGCC ATCTGCAGAA CTGTCCTGCA AGTACTTGTT 600 GGCAAGGTCC TGCAGTTCCT TTGCCTACGG TTCTTTCCTT CCCTTAAGAG GCCCAGCACT 660 TGCCTGGCCA GATTATGTTG TAGCTTGACC CTAGTTACTG 700
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