Tag | Content |
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EnhancerAtlas ID | HS108-16015 |
Organism | Homo sapiens |
Tissue/cell | K562 |
Coordinate | chr17:1453930-1455360 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Mafb | MA0117.2 | chr17:1454100-1454112 | CGTCAGCAGTTT | - | 6.02 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_27390 | chr17:1453195-1454949 | Esophagus |
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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 |
GH17I001550 | chr17 | 1454241 | 1454450 |
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Enhancer Sequence | TCCCACCTCA GCCTCCCAAG TAGCTGGGAC TACAGGTGCA CACCACTATG CCTGGCTCAT 60 TTTTGTATTT TCTGGTAGAG ACAGGGTCTT GCTATGTTGC CCAGGCTGGC TAAAAGGTCC 120 TATAAGTTAT GTCAGACAGC ACGGACTTCG TCCTGAAGGC AAAGGGAAGC CGTCAGCAGT 180 TTTGGCGCTG GGAGTGACAG ACCATCCAGA CTGAACACTT GAAGCGGTGC GGAGAACTGA 240 AAGGCAGGGA GACTCGTTAG AAGCTGCTGT AGTAATCCAG GCAAGAGGTG GCAAGGAAGG 300 GACATGTTGG AGACGCTGAG GAGATGGAGT CAGCAGGACC TGATGGGACA CGAAGGGCAA 360 GTGAGAGTGT TGCGGGGCGG AGTCAGCGGG ACCTGATGGG ACACGAAGGG CGAGTGAGAG 420 TATTGCGGGG CGGAGTCAGC GGGACCTGAT GGGACACGAA GGGCGAGTGA GAGTGTTGCG 480 GGGCGGAGTC AGCGGGGCCT GATGCGATAA GAAGGGCGAG TGAGAGTACT GCAGGGGAGC 540 TCTGCTTTCT GCTTTGGGCA GCCAGATGGC TGACACAGTA AAGCTTCTCT TGTCACCATG 600 GGGAGAGGTA GTGGTGGCAG TCACTGCTGG CCTTTTCTTT TTCTTTTTTT TCTTTTTTTT 660 TTTTTGTAAG AGACAGGCGG GATCTCATTC TGTGGCCCAG GCTGGAGTGC AGTGGCGTGA 720 CCATGGCTTA CTGCAGCCCT GACCTCTTGG GCTCGGGTGA TCCTTCCACC TCAGCCTCCT 780 GAGTAGACAG GACTACAGAC ACTCGCCACC ACACCAGCCT AATTTTGTTT ATTTTTTGTA 840 GAGATGGAGT CTCGCTATGT TGCCCAGGCT GGTCTCAAAC TCCTGACCTC AAGTGATCCA 900 TCCGTCTCGG CCTCCCAAAG TGCTGGGATT ACAGGCGTGA GCCCCCGAAG CACCCGGCCA 960 GGTTCCATCT TTCATATGTA GAGACCTCGT CTCTGTCAGT TTGGTTGGAC CAACTTAGTC 1020 TTGAGGAAAC AATTGGTCCC TTCTACCTAA AATACCAACT TCACCATCTC TTTTCAAAAT 1080 CCTCTTTAAG AAATACAAAT ACCAGAGGAG GAGCAAAACG AGACATGGAG AAAAAGTGTG 1140 CTGGTGAGGA GACTGAGTGA TGGTGAGGTT CCTCCCCGCT GGACAGCACT GCTCTCCTCG 1200 CACCCCGGCA CTGAGGTCCT GGACCCTCTG GCGAGGAGAC TGGGTGACGG TGAGGAGACT 1260 GGGTGATGGT GAGACTCCTC CCCGCTGGAC AGCGCTGCTC TCCTCGCACC CCGGTACTGA 1320 GGTCCTGGAC CCTCTGGCGA GGAGACTGGG TGATGGTGAG GTTCCTCCCC ACTGCACAGC 1380 ACTGCTCTCC TCGCACCCTG GCACTGAGGT CCTGGACCCT CTGACACCAT 1430
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