Tag | Content |
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EnhancerAtlas ID | HS147-08204 |
Organism | Homo sapiens |
Tissue/cell | NHEK |
Coordinate | chr11:18033060-18034490 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
TFAP2C | MA0524.2 | chr11:18034225-18034237 | TGCCCCGAGGCA | + | 6.14 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_35602 | chr11:18032257-18034670 | HepG2 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr11 | 18033400 | 18033779 | chr11 | 18033800 | 18034338 |
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Enhancer Sequence | CTGTGAGAAA ATAAATTTCT GTTGTTTAAG CCTCTGTTGT GTGGTATTTT GTTATGGTAG 60 CCCTAGCCGA CCAACACACC CCCACAGTTT CAGATTATAC AGCAGGAAAA ACACACTACC 120 AGTCCTCCAA ACACAGCAGA AGGGTGTCAA CAACCTATTA AACATATTTT ACAACCTTTA 180 ATATTCGGCT TTGTCTGTAC TGAAACAATA TTTCTGTTTC CTCTGTCCAC ACAGACGCCA 240 GTCTCCTGCC TGGAAAAAGC CAGAGACAGC ACACATTCAA TCCCCAACTC CACCCCCAGC 300 TCCCGGGCCA CCTCAAAGAC GCCCAGCCAG CCAGACTACC GCAGGTCACG CCATGCTCTC 360 CCTCCTGCCA AATTGCAGCC CCACATTCAA CAATTGCCGC CTTGTACTGA TCATTACTTC 420 TTTAAAAATT GGACAACTAA TACTGATTTT AACAGCAATA CAGGTTATAA TTTTGCTCTC 480 CCCCAACACA AGAGCTGGAA GTCCTTCACT CGTGTATTTC ACTCATGTGT ATTTCCCCAA 540 CACCAGCACA TGGGTAGGCA CACAGATGCT CGTTCATTCA TTCGTCAACG AGTATTTACT 600 GGGGACCTAC AATGTGCCAG ACACCAAGAG AGGCACCGTG AACAAGACAG GCACAGCACC 660 CACTCTTACC ACACTTACTT TCCAGCCAGA GAGACTGACG TTAATAATAA ATTATACACA 720 TCATTACAAT TGTGATACGT GCTATGAAGA AGCACAAGAC GCAGCGACTG CTTGTTCCCG 780 TGCATGCTGG TCGGCCACCT GCCACGCTCC TGTGCATGAA CCCTCCTCTC TCCCAGACAC 840 ACATCAAGAT GACCCTGTCT CTCCCAATGC TCCCGTCAAA CCAACAGCAG CCCAACTCCC 900 CCAACACATG CAAGAACCGG TCACAGCAGA GTGTCAGCAA ATAGGCAGGG TCTGTGCCTT 960 GTGCGCGGCC AAACACCGCA GGCCTCACAT CTAAAGGATG CTTTCGCCAG GCTGGGACAG 1020 GGTCTCCCTC CTCCAGGCAT CAGGAGTGTG GGGGGCACAG GTGGCCCCAC GGAGCTCTGG 1080 GACCGGGCGA TCCTCTCCAC CGAGCCCTCC GCGCTGTCTT CCAGGCGCTA TTCGGGCTGG 1140 AGGGCTCTCG CGGAACCAGA CGCTCTGCCC CGAGGCAGGT TCTTCCCGCG GCGCCACAGC 1200 CCCTCCGGCC CTGACCCCGC CAGCCGGCAG GCCCCTAAGT CGACCGCGAA GACCCTTCCT 1260 TCCCCGCCCG CCCGCTCCTC CTCCGCTCCC CCTCCGCTCC CAGCCCAGGA TCCTTCAACC 1320 CAGAGCCCGG CTCGGACCTC AGCCGCCCAG CCCCTGAACT GCCCACGCCG CGGCCAGCAG 1380 CTCCCACATC TCGGCGCCCC TCAGGGCCTG CACCGGCCCG GGGGCGGAGT 1430
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