Tag | Content |
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EnhancerAtlas ID | HS187-21618 |
Organism | Homo sapiens |
Tissue/cell | Th1 |
Coordinate | chr6:111265410-111266600 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Nfe2l2 | MA0150.2 | chr6:111266047-111266062 | TGCTTAGTCATAATG | - | 6 | Nkx3-2 | MA0122.3 | chr6:111266088-111266101 | ATAACCACTTATA | + | 6.33 |
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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 |
GH06I110944 | chr6 | 111265441 | 111266802 |
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Enhancer Sequence | ATACTCCCAG CTACTTGGTA GGCTGAAGCA GAAGAATCAC TTGAACCAGG GAGGCAGAGG 60 TTGCAGTGAG CCGAGATCAC GCCATTGCAC TCCAGCTTGG GCAACAAGAG CGAATCTCCA 120 CCTCAAAAAA AAAAAAAAAA AAAAGCTTTG GATTTTGGAG AATTCTGGAT TTTAGATTTT 180 TGGATTAGGG TTGCTTAACC TGTATCAACT TTTCAAGTTT TAGGAACGCA GATTTACTCC 240 TGCCATCTCA AGTAGTAGGA AGTCTCTCTA TACACATATT TTATAAAGAG ATGGGGGTCT 300 TGCTATCTTG CCCAGGCTGG TCTCAAACTC CTGAGCTCAA GTGATCCTCC CGTCTCAGCC 360 TTCTGAGTAG CTGGGAGGAA GTCTATTTTG AGGATACACA TGACAAGAAA GATGAGAATA 420 TCATAGGAAC TTAAGAACAG TCAAGTGGTT AGACTGCAGT TGGGAACTAA AATGAACATG 480 GAAGTGGACA ACAAATTCTA TGCACACCTA CAGATGGAGT TAAGTGTCAC TCTCAGTGGC 540 AGGAGTCATG CAGTACTCCC CAAACCTGAG GGTGTGTATC ACCATTTCTC TCTGTCTCTA 600 TGACTACCAG CCAACTACCT CATTTAGTCA TAGCTTCTGC TTAGTCATAA TGCCAGTTTA 660 CTCATATCAT GTCTCTCTAT AACCACTTAT AACCACTTTT AGCTTCTCTC CCCACATTCA 720 ACAGACTGAT TCTCTGTATA ATCAACTTCA AATTCTTTTT CTCTTTTTTT CTTTTTTTTT 780 TTTTGACAGA GTCTCACTCT GTCACCCAGG CTGGAGTACA GTGGCGTGAT CACAGCTCAC 840 TGCATCCTTG GCACCCCAGG CTTAAGCAGT CCTCCCACTT CAGCCTACTG AGTAGCTGGG 900 ACTATAGCTG TGCCACCATG CCTGGCTAAT TTTTTTTTTT TTCTTTGAGA TGGAGTTTCA 960 CTCTTGTTAC CCAGGCTGGA GTGCAACGGC ATGATCTTGG CTCACCGCAA CTTCTGCATC 1020 CCGGGTTCAA GTGATTCTCC TGCCTCAGCC TCCCAAGTAG CTGGGATTAC AGGCATGCGC 1080 CACCACGCCC AGCTAATTTT GTATTTTTAG TAGAGACAGG GTTTCTCCAT GTTGGTCAGG 1140 CTGGTCTTGA ACTCTCGATC TCAGGTGATC TGCCCACCTT GGCCTCCCAA 1190
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