Tag | Content |
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EnhancerAtlas ID | HS145-07815 |
Organism | Homo sapiens |
Tissue/cell | NHBE |
Coordinate | chr14:101213210-101214120 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOS | MA0476.1 | chr14:101213605-101213616 | TCTGACTCATT | + | 6.32 | Zfx | MA0146.2 | chr14:101213254-101213268 | CCCGCCTCGGCCTC | + | 6.01 |
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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 |
GH14I100746 | chr14 | 101213029 | 101214382 |
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Enhancer Sequence | AAGTTGGCCA GGCTGGTCTC AAACTTCTGA CGTCAGGTGA TCCACCCGCC TCGGCCTCCC 60 AAAGTGCTGG GATTACAGGC ATAAGCCACC CCGCCTGGCC AGTTTTTATT TTTTTATACT 120 GTATTTTTAC TGTACCTTTT CTATGTTTAG ATACACAGAT ACTTACATTT TGTTACAATT 180 GCCTGTAGTG GTCAGTACAG TCACATGCAG TACAGGTCTG TAGCCTAGGA GCAATAGACC 240 ATACCACCTC GCTCCGGTGT GCAGTAGGCT GTACCATTTA AGTGTCTGTG AGTACACTCT 300 ATGATGTTTG CACAACAACG CAATTGCCTA ATGATGCGTT TCTCAGAACA TACCTCTTTG 360 ATTAAGTGAG GTATGACTGT GCTTGGGCGT GCTATTCTGA CTCATTTACT GAGTGATGTG 420 AAAATCTGCC AATTTTGAGA GAGACCCAGA ACAAGAGAAG GCTGCACAGC AGATCCAGGC 480 TGCCGTGCCA GTGGCTCTGC CTCTTGGGCC ATATGAACCA GCAGATCCAG TGGTGTCTGC 540 AGTGTCAGAG GCACTTCCCT GGGGAGTTGT TCCGAGCTTT TGGCACCCCC TCCCAGGTGA 600 ATCACAGCAC AGACCATTCA CATTTTGGAG TGAGGTGCTG CCCTCCTTTG TGGAGAACCA 660 CTCTCCGCTC GGGTGTCATT GAGAAACCAC TTTTGACTTG CTCCTGGGCT TCCACAGAGA 720 TTGAACTCTT TTTTTTTTTT TTTTTTTTTA AGACAAAGTC TTGCTCTGTT TCCCAGGCTG 780 GAGTGCGGTA GCGTGATCAC AGCTCACTGC AACCAACTCC CCGGTTCAAG CAATTCTCCT 840 ACCTCAGCCT TCCAAGTAGC TGGGATTACA GGTTCCCAAC ACCACGCCTG GCTAATTTTT 900 GTATTTTTAG 910
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