Tag | Content |
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EnhancerAtlas ID | HS145-09828 |
Organism | Homo sapiens |
Tissue/cell | NHBE |
Coordinate | chr17:18917030-18918360 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Klf1 | MA0493.1 | chr17:18917848-18917859 | AGGGTGTGGCC | - | 6.32 | NFYA | MA0060.3 | chr17:18917374-18917385 | AGCCAATCAGA | + | 6.32 | RUNX1 | MA0002.2 | chr17:18917725-18917736 | AAACCACAGAG | - | 6.14 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_26604 | chr17:18916816-18919232 | Esophagus |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr17 | 18917257 | 18917349 | chr17 | 18917640 | 18918133 |
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| Number: 1 | ID | Chromosome | Start | End |
GH17I019013 | chr17 | 18916817 | 18919232 |
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Enhancer Sequence | AACATAATGA CACAGGGAAA ATGCTGGGTG CAGGCTTGGC CATGCTGTAG TTCCCACCTT 60 GGGCCTTCGC TTTTCTCTTC TGTTCTGGGC AAGGGGACTC GCTAAGCCCT CCAGGGCTGA 120 CACCGAGCCA TTGTTGGGCC ACAGTCCCTC TCTAGGTCTT GAGTTCCCTC TCTAAGAAAT 180 GGATGGAATA AGCTCCAAGT TCATCCATCT CCATGAGCAA GACAAGGGAG TGGGTGGAGA 240 AATGTTTTGG GGAAAACTGT GATTTGACTC ACTTTCCTTT GGGCTCCATC CCAACCAGCT 300 TCTGACAAGT GAACAGAGAG CCCAGAGACA CCTGGAAGTC ACACAGCCAA TCAGACACAG 360 AACCGAGGCC AGACAACCCA GCCAGGCAAT AAATGGCTGT GCCTTCCGGG CAGGGGGGCC 420 TATGTCAGGC TTATCCTAGG ACAGACGGGC AAGAGTTTGT AGAGGTAAAG GAGGTGCTTA 480 AAATTGCAGG AGTTCTTGTA GACAGACTTG AACTCATCCC CAGAGAGGGG AGGCGACCAG 540 CCTGAAGCCA CACAGCACAG AGTGGGCAGT TGAGCATCCT TCCACCTTCC TTAGGGCTCC 600 TCACCCTCAG GCCCTCTTGA GCCCACAACT CCCAGAAGGC CTTTCACAGC AATGCTACCC 660 GCACCTCCTA GGGGAGCCCT CACTCCCACT CTGGAAAACC ACAGAGCCAA GGAGAGAGGG 720 GATCCACTAT GCCTGCTGGG TCCTGCCATG CACAGGAAGT GGCGGAAAAT TCCAGAGACT 780 GGGGCACTGC ATGCTGGGGT GAGGTGTGCA TCTTGCCCAG GGTGTGGCCT TCAAGCAGAG 840 GCCCCGCCCA AGCCTTCCTC ACCAACCCCA CCGCACCCCA AAGTCCTGCC GCTGGCCTGC 900 TGTGAATCCC TGGGCAATCT CTTCACTTCT CTGAGCTTCC ATTTCCTCAT CTGTCAAGCG 960 GGTTAATCAT GCTTTCCTCG GACGAAGGCA TGGGTGTGAA AGTGCTTTGT CAACGCCAGG 1020 CTCTGCAGAA AGGACAGGCC TGATCGCAGC CTCAGCATTA TGAGTAATTA TGGTCGGGCC 1080 TAGGGTTGCC AGCAAGCCTA GGGCTCAAGC AGCCAGCTCC GAAGTCCCCA CGGTTTGTCC 1140 TTGGCCTCCC CAGTCTCCTC ATTCTGGGTC TTGCTCACCT CAAACCTCCT CAGCTTCTCT 1200 CCCTCCCCGC CCTCTGCCTT GGAGGAGCAT GCAAATGGCG GGCGGGCCTC AGGCATTAGA 1260 GCCCAGGCGG GAGGGGTTCC CGGGGCTGTC TCAAGGCCGG ACAGGGTCAC ACATCCCCCG 1320 TCCCACCCCA 1330
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