Tag | Content |
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EnhancerAtlas ID | HS145-27153 |
Organism | Homo sapiens |
Tissue/cell | NHBE |
Coordinate | chr9:140163060-140164430 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
NFE2L1 | MA0089.2 | chr9:140163124-140163139 | TTTGCTGTGTCATCC | - | 6.33 |
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| Number of super-enhancer constituents: 4 | ID | Coordinate | Tissue/cell |
SE_32084 | chr9:140162284-140164794 | Gastric | SE_41683 | chr9:140162158-140164915 | LNCaP | SE_43354 | chr9:140162160-140164795 | Lung | SE_60158 | chr9:140160788-140173695 | Ly4 |
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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 |
GH09I137267 | chr9 | 140162144 | 140164480 |
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Enhancer Sequence | CTCCCAGTTC TGCGGGCTGG GATGGGAAGT CCGAGGTCAA GGGGCCTGCA TCTGGCTGGG 60 GCTTTTTGCT GTGTCATCCC ATGGTGGAAG GCAGAGGGCA AGAGAGCACG GGCAGGGGAG 120 ACAGACAGAC ACAGACAGAG ATGAGAGACA GAGACACACA GACCAAGATG AGAGACAAAG 180 ATGAGAGACA CAGAGACAGA GATGAGACAC AGAGAGATGA GAGACAGGTA AGAGAGACAG 240 AGACAGGAGA GACATGGAGA CAGACAGATG AGAGACACAG GACAGAGACA GATGAGAGAC 300 AGAGCTAGAG ATGAGACACA GACAGACGGA GACAGAGAAG GGGCCACACT TACCCTTTTA 360 TCAGGAGCCA CTCCTGTGCT AACAGCGAGA ACGCTTTGGT GAGGACGGAG CCCTCACGAC 420 CTCAGCAGTG TTGCGTTGGG GATCAGGTTT CCGATGGTGA ACTTGGGGAC ACGTCCACAC 480 CACAGCACGT GCCTATTGTG TTTCTCGGTG GCTGGTGTGT TTGAGGATGG CGCGTGCATG 540 CGTTTTCCAG CTTTCTTTGT GGAGGAAGTT ACCTGTGGGT ATTAACCTGT CCCCAGCCAT 600 CCTCTCACTG AGCTTGGGTT GCCTGGGCCT GGGTTTCCTG TTGTTGCTGG AACGAATGAC 660 CACAGACAGT GGCATTAGAC AGCGCAGGCA GACATGACCT CCTGGGCTTC TGCGGGTGCC 720 AACACTGCCG CTCCTTCTGG AGGCTCAGGG AGGCTCTTGA GGGCATTGGG ACATCGTGCT 780 GCCGGCCGCC GGGCAGAGCC GGTTTGTTTA TTTTTTGAGA CTTCCGGGAA CATAGTTATA 840 AATAACTTTA ATTTGCCTTG GCCTGCCCAC TGCAGTACAG TCACGTGTCA CATAACATTC 900 TGTCTACCGT GGACCACATA TACGACCACG CGGTCACATA AGCTGACAAT ACTGTATTTT 960 TACTCCACTT TCTCTATTTA GATACACAGT TGCCATTGTG TCCCAGCAGC CTTCAGTACT 1020 CAGTACAGCC ATGTGCTGTG CAGGTGTCTA GCTCAGGGGC ATGAGGCCAT GGCCCAGCCC 1080 AGTGTGCAGT GGGTGGCACC TTCTGGATTT GTGTCAGTCA CTGTGGAGTT CGCACAATGA 1140 CAGACTCACC TGGGAGGCCT TCCGTGCGCT TCTGTTTCTT TCTCTCATTT GATTGTGGCT 1200 AGAAACAGGC TGGGAACCAG GAGTGCAGCT TCTCGGAGTA CGTGGCTGCC CCACGGGGTG 1260 GGATGTGCAT TTTCAGTCAC ATTTGGGGAG AGCACGCGTG TTCTTAAGTT TTTAGCGGGT 1320 TCTAGTAAGA ATGGATGTTG ATTTTTAGAA TTCTCTCCTG TTTATTTTTT 1370
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