Tag | Content |
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EnhancerAtlas ID | HS176-05692 |
Organism | Homo sapiens |
Tissue/cell | SK-N-SH |
Coordinate | chr10:86070150-86071320 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
NFE2L1 | MA0089.2 | chr10:86070366-86070381 | CCTGCTGAGTCACAG | - | 6.03 | Nfe2l2 | MA0150.2 | chr10:86070368-86070383 | TGCTGAGTCACAGTA | - | 6.57 |
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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 |
GH10I084307 | chr10 | 86067538 | 86070589 |
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Enhancer Sequence | ATTTCCTGCC TTTCCAACCT GTAGGAAATA CTTCAGCTTG AAACTTCCAC CCTGCTCGGT 60 GCATGAGCCA GAGAGGTGCA TGGAGTGTGC AGGTAGAATG GAGCAGAGAG ATACAGAGGA 120 TTTTGGAACT GTTCTTTCAA GAGGTTTGAT TCTAATATGC CCAGGTTACC CAGCTGACTC 180 CATGGGAACC TACATGCGCA TAGAGCCTCA GCCTAACCTG CTGAGTCACA GTAGCAGGAA 240 CAGACTTCCA GCTTCTCCCC ACATGAGCAG GCCACTCACT CCTCAGAGGC ATTCATCCTT 300 TTCTGATCTC TGTTGGAAGA ACTGGCTACT GGCCAGAGGC CTGGGATGAG GATCCTCTCC 360 ACAGCTGACC CCAAGTACCA AGGAAATTGG AGGCAGAACT GGCATAGGAG CCAGTTGGGA 420 AGAAGTGAGG GAGGTGGCAC TGGGTCACTA TACTGATGGT TCCCCATCGC TAGCACCACC 480 ACTGGGCAGC GGGGCATGGG CATGTTTACC CAACTTAAAG ATCCAGGGCA ATTTTCGTAG 540 TTTTTGAGAG AAGCCTTTCT GGGTTGCTGG TTCCTGGTCC CCAGCCCAGC TCTAAGCCCA 600 ATGGGTCAGG AAGTGCTCAG GGGCTGCCAA CTGACTTAGG GTATCCACAC TGCTTGGAGA 660 AGCTGCTTCT GAGCCCTATC CACTATGTCA GGCTGAGCCA GATGCCAGCT CACATAAGTT 720 ATATTTGCTA TAACCTCTGC ATGGCAACTG GGAATCCTGA GTCCTCTTCA CAATGTCCTC 780 AGTTCTCCTA GACTGGGGAT CATCCATCAT CCCTTTCCTA CCTGGCCCGT TACTGGGCCA 840 ACTTCCCAGA TGGGACGGAG TTGGCTGGCA GGCAGACCTC AGAAGGGTCC ACTGTCTGAG 900 AATGAGGTTG AGCATCAGGG AGAGCTACTG AGCTTTGAAC AAGCCAAGAG AAATGTTTCT 960 TGTAACTGTG GCTGGAGTCT TCTGCCTGGA AAGATAGGCA GGAGATACTG CTTCAACAAC 1020 CAAAGGAAGC AGGAGACATC CCACTTGATG ACCCCAATAT TTCCCTGCTG CCATAAATGT 1080 GTTTTTTCTT TTTTAAATAT TACCTGGTCC CATTGTTCCT TCCGGTGGGT TCGTGGTCTC 1140 GCTGACTTCA AGAATGGAGC TGTGGACCTT 1170
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