Tag | Content |
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EnhancerAtlas ID | HS116-03479 |
Organism | Homo sapiens |
Tissue/cell | Left_ventricle |
Coordinate | chr1:237450990-237452530 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
NFE2L1 | MA0089.2 | chr1:237451857-237451872 | TCTGCTGAGTCATGC | - | 7.23 | Nfe2l2 | MA0150.2 | chr1:237451859-237451874 | TGCTGAGTCATGCAG | - | 7.41 |
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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 |
GH01I237288 | chr1 | 237451321 | 237451450 |
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Enhancer Sequence | CTTGAATATT TCTCCCTTCA CTTCTTGTAT CATTTTTTGT ATTTCCTTGC ACGGGGCTTT 60 GCCTTTCTCT GGTCCCTCCT TGATTAGCTT AATAACTAAC CTCCTGAATT CGTTGTCAGG 120 TAAATCAGGG ATTTCTTCTT GGTTTGGAGC CATTGGTGGT GAACTAATGT GATTTTTGTG 180 GAGTGGTGAA GAGCCTTGTT TTGTCATATT ACCAGGTTTG GTTTTCTGGT TCCGTCTCAT 240 TTGGGTAGGC TCTGTCAGAG GGAGGGTCTA GGGCTGAAGG CTGTTGTTCA GATTCTTTTG 300 TCCCACGAGG TGTTCCCTTG ATGTAGTACT TTCCCCCTTT TCTTATGGAT GTGGCTTCCT 360 GTCAGCTGAA TCACAGTGAT TGTTGTCTGT CTGCTGGATC TAGCCACCTG GTGAGTCTAC 420 CCAGATCCAG GCTGGTACTG GGGGTTGTCT GCACAGAGTC CCATGATGTG AACCTTCTAT 480 GAGTCTCTCA GCTGTGGATA CAAGTGTCTG TCCTGGTGCA GGTGGTGCGA GTGTGCAATG 540 GACTCCATAA GGGTTCTTTG CTTTGGTGGC TGAATGCTCT ACTTTTGTGC TAGTTGGCTG 600 CCTGCCAGGA AATGGCACTT TCCAGAGAGC ATCAGCTCTG GTAGTATTGG GAGGAACTGG 660 CGGTGGGCAG GGCCCTAGAG CTCCCAAGAT TATATGTCCT TTGTCTTCTG CTACCAGGGT 720 GGATAGGGGA GGACCATCAG GTAGGGGAGG GCTAGGCACG TTTGAGCTCA GACTGTCCTT 780 GGGTGGGTCC TGCTGCAGCT GCTCTCGGGG GTGGGGGTGA GATACCTAGG TTACTGGAGT 840 TGTGTACCTA GGAGGATTAT GGCTGCCTCT GCTGAGTCAT GCAGGTTGTC AGGGAAGTGG 900 GGGAAAGCCA GTAGTCACAG GCCTCACCCA GCTCCCACGC AAACAGAAGG GCCAGTCGTA 960 CTCCCACTGT GCCCCCCAAC AACAGCCCTG AGTCTGTTTC CAGGCGGAGG GTGTGATGGG 1020 TTTGAACACT TACCCCAGGG TACCTGCCTT CCAGCTGCAA AATAAAAGGG CTTGGTTCCT 1080 CCCCTGCCTA TGGAGTCTGG ACACTAGATT TGCACCCTCC CCTGAGTTCT GGCCAGGAGG 1140 CCTCTCACCC CATTCAAATT GTTACAAAGG CCAGCTAGAG ATTTCCTTCT GCCTGTGGAG 1200 TTTTACCCCG TGCTCCTCTC CCATTGGATC CCTGTGGTGC CAGGCAGGTA TGGGGTGCTT 1260 GGGGACCCAG CGAGCTCCCA GGGCCTTTCT GCTGCTTCCT TTACCCCCTG TATGTTGCTC 1320 AGCTCTCCAA ATTGACTCAG CTCCAGGTAA AGTTGTAAAC TTTTCACGCA AACAGACCTT 1380 CGGCTTCTCC AGTGGGGGTG TATATTTGGG AGAGGAGGGC CGCCCTTTCC TACTTCCATG 1440 GTTGGGGCAC TCACAGTTTT AGGGGGGTCT CCCGGGTCCT GCAGGAGCAG TCCGCTTCCT 1500 TCAGAGGCTC TGTGGATCCT CTCGGGATTG CTGGTTTGTT 1540
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