Tag | Content |
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EnhancerAtlas ID | HS147-09347 |
Organism | Homo sapiens |
Tissue/cell | NHEK |
Coordinate | chr11:77312770-77314190 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
MAFK | MA0496.2 | chr11:77313564-77313583 | AATTGCTGAGTCATGAATG | + | 6.35 | NFE2L1 | MA0089.2 | chr11:77313565-77313580 | ATTGCTGAGTCATGA | - | 7.6 | Nfe2l2 | MA0150.2 | chr11:77313567-77313582 | TGCTGAGTCATGAAT | - | 6.3 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr11 | 77312851 | 77312937 | chr11 | 77312988 | 77314161 |
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| Number: 1 | ID | Chromosome | Start | End |
GH11I077601 | chr11 | 77312492 | 77315150 |
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Enhancer Sequence | CTGCATTCAG CTGACCAGTG GTGAGGCTGG AAAGCCCAAG GTAGCCTCAC TCATATGTCT 60 GGCAGTTGTC AGCTGTCATC TAAGATGCCT CAGTTCTCTT CCGTGTGGCC TTTCATCCTC 120 CAGCAACCTA GACCAGCAAA CTTACATGGT CAGGGCATTC TTCCAAGAGA GCAAAAAGTG 180 GAAGCTGATG GGTTTATTGA GATGTGAACC TAGAATTCAC ACAGCATCAC TCCTGTTACA 240 TTCAGAATTC CCATAGCCCT ACTCTGCTGC ATTCTATCAA CACAAGTTGC AAAGCCAGCT 300 CATTTTTAAG AGAGGGAAAG TAGACAACGT CTTGCTGGGA GAAGCAGCTA CCACTAAGTC 360 ACACTGATCA GAACTGCTGT GTGAGGATGA GAAGATTAGG AAGTGAAGTC GTTTGAGTTT 420 TAGGATGGCA TAAGACTGAT CAGTGGTGTT CATCTTAGAT CTAGTGGAAA ATCTTCAGTA 480 TACCATGGCC TTGAATACTG AAGTAAACTA AGTGAGGGTA ATGATTCAGT CCATTTTTAT 540 CAATACATGC CTAAAAGTCA CAGGTCATTT ATATCATCAT AGGTCATATT ACATTATATT 600 GTAAATGTCT GTGTGAGTCT TTATCTTTCT GCCCATGGTA TCTAGTACAC AGGAACTCAA 660 TAAGTTTTTG TGTAATCAAA CTGAAATGAC TAGCTGCCAA CCAGACAATT CTGTTCACCC 720 TTAGCAGTGG CAGGTTTAAC ATTCCAGGAT TTGACTGTTC AAGAATGATT CCAAAGGTCT 780 ATGATATCAT TTATAATTGC TGAGTCATGA ATGTGAATCA TGCTGTGAGG CTGGTACACT 840 AGAAAAAACT CTTAGCTATT GAGTGAGCTT AGTTCATTGC TAAATATCTT CATCTCAACA 900 CAGCTTCATT GTTCTCGGCC TATTCAAGTG TGAAATCTCA GTAGTGAAAT CTTATGAAAG 960 GGCCACTTAA TTTCCATGAA AACAGGCTAC AATGGTGCAT GTCAATAATA AAACTTCTGA 1020 AGATCTCAGG ATCTATCTCT GTGGCTAAGT AAAAGAGGCA GAGTTGTGTG CCTAAGCTTC 1080 CACTTGGAAA AACTGCTGAA AATGTCACTG TCTGAGGGAT GCTCTTAGGC TGGACTTTGA 1140 AAAGCGAAGA CACAGCTCTG TGGAGTACTG CTGGACAGGC ATCCAGCCTC CTCTTCCATT 1200 CCGCACTTGT GTGGCCAGAC TATAGACTCC TAGCCCCATG CCAGAGAAAT ACCCTGGGTG 1260 CAGAGCTGGA ACACAAATCC TAAAAAGTAG CCAACAGTTA TAATTTGTGC TTATCTCTCA 1320 TGACTACTCA CAGTCCCTTC TTAAGGGCTC TGTTGACAAG TAAAAATAGA ACCAATGATA 1380 AAGCTTTGGT CTATTGGTCC ATTTTACCTT TTCAATACAA 1420
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