Tag | Content |
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EnhancerAtlas ID | HS148-00361 |
Organism | Homo sapiens |
Tissue/cell | NHLF |
Coordinate | chr1:40605690-40606700 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Myog | MA0500.1 | chr1:40605788-40605799 | AACAGCTGCAG | + | 6.02 | Tcf12 | MA0521.1 | chr1:40605788-40605799 | AACAGCTGCAG | + | 6.62 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr1 | 40605800 | 40606000 | chr1 | 40606000 | 40606476 |
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| Number: 2 | ID | Chromosome | Start | End |
GH01I040140 | chr1 | 40605873 | 40606190 | GH01I040141 | chr1 | 40606256 | 40606595 |
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Enhancer Sequence | AGCCTCTTTA CACTGGCTCC TGTGTTCTTT TGACATTTCT CATCTGTATT AGTTTGCTAT 60 GCCTGCTGTA ACAGTGTACC ACAAACTCGG TGGCTTAAAA CAGCTGCAGT TCTCATGGTT 120 CTGAAGTCCA GACATTCAAA ATCAACTTCA CTGGGCCCAA ATCAGGAATA TTAACACGGC 180 CATGCTTCCT CTGGGCTCTA GGGGAGAATT CGTTCCTTGC CTCTCCCAGC TTCCAGCTGG 240 CACTTGGCTT GTGGCTGCAC CACTCCAGTC TCTGCCTCCT GCCTTCTCCT TTTGCGTAAT 300 CTCTCTCTGC CTCTCTCTTA CAAGGATACT TGTGTTTGCA TTTAAAGTCC ACTTGAATAA 360 TCCAAGACAA TCTCCCCATC TCAAGTTCCT TGATCATATC TCTAAAGATC CTTTTTCTGT 420 ATATGATAAT ATTTACAGAT TCCAGAGATT AGAGCTTCAG GGGCCATTAC TTAGCTTACT 480 ACATCCTCAT TCTTTGAATA CTTCCTTTCT TCCTGAACCA GTAAGATTTT TCACTGCCCT 540 AGTCATGAAA TCAGCCATTT CTCTAAGAAC TTTTGGTTTC TTTTTAGTGA AGAATGATAC 600 TTGGAAGTCA AGATGTAGAT GCTAGGTGCA CTCATTGCTA TGGGTGTGTC GGTCTTGCAA 660 GTCCTTTCAG TAGGACAAGG AAACAAGATA TCAACTAGGA AAAATATGTC TGGACACACA 720 CACACACAAT CATACGTATG ATGTACATTC CGAAGTACTG TAGTGGAGTT GGCTCATATG 780 GACTTGCAAA AGCTGCTTGT TAAATATTCA GGAACTTTGC GGGTGGCTGT GAAACTAGTA 840 TTATTTCATG CTGGGAGTAT TTACACCGTG GAAATCAGCA AATGCTACAA ATTAGTGTGT 900 TTTGAAAAAC CAAAAAGCCA CTATACATAT CATAAACACA CACATCTACT CTTCTGTCTC 960 TCTTTGTATA TCATATATAA TATTCACACA CACACACACC CTATAGGCTC 1010
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