Tag | Content |
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EnhancerAtlas ID | HS145-09634 |
Organism | Homo sapiens |
Tissue/cell | NHBE |
Coordinate | chr17:4150880-4151850 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOS | MA0476.1 | chr17:4151109-4151120 | GGTGACTCATT | + | 6.02 | Klf1 | MA0493.1 | chr17:4151503-4151514 | GGCCACACCCA | + | 6.62 |
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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 |
GH17I004246 | chr17 | 4149624 | 4152890 |
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Enhancer Sequence | AGTGCTTATG GCTGAGACAT TACCAGCCCG TGGGGAATAC TGTCTGCTTA CAAACAGCAA 60 TGCAAATGTG TCCTTGAAGT GTCACCAAGC TGTACAGTTC TTACAAGAAA AAGTACAACA 120 TTATTCTGAG CAAAATGGAG AGAGAATTTA CAGTGTGCAG GTTCTAGGGC CAGACTGACT 180 GGGATCAAGC CCAGCCCCAC TACTGCCTAG TTTTGATACA CCTTAGGCAG GTGACTCATT 240 CTCTTCACCT GCAAGGATGT TGTAAACACT GAAAGTACTA ATACATGTAA TAACCTTAGA 300 ATACAACCTG CTCTGCAGTA GGTGGTCAAA ATATATTAGC TATTATTACA ATTCTTAGAA 360 AGGCAACCCG GGGTAGTCAG TCCTGTGTTG CAAGATTCTC CCTGCACACT GATAGCCCAG 420 AGCTCGCATT CCAGAGTCTC ACTGACTGGG TTTGACCCCA GCTTACCCAT TTACTAGCTG 480 TGTGACCTTG GGCAAGTTAC TTACTTCCTC TCTGTGCTTC AGTCTTCTCA CATGGAAAAT 540 GAGACTAATG ATACTATCTT AGAGCAGGTG TCCCCGACCT CCAGGCCGTG GACGGGTACT 600 AGTTTGTGGC ATGTTAGGAA CTGGGCCACA CCCAGCAGGA GGTGAGCTGC GGGCGAGTCA 660 GCATGACCAC CTGAGCTCCG CCTCCTGTGA GATCAGCAGC AGCATTAGAT TCTCACAGGA 720 GCGTGAACCC TCCTGTGAAC CGCGCATGCG AGGGATCTAG GTTGCATGCT CCTTATGAGA 780 CTCCAGTGCC TGATGATCTG AGGTGGAACA GTTTCATCCT GAAACTACTC CCTTCCCTAC 840 CCCATCTATG GACAAACTGT CTTCCACGAA ACCAGTCTCT GGTGCCAAAA AGATTGGGGA 900 CCACTGTCAG AGAAGTACGT GTAAAGTCAT TAGGATAGGT TAAATCACTC GGAACAGTGT 960 CTGGTTTAGT 970
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