Tag | Content |
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EnhancerAtlas ID | HS113-05477 |
Organism | Homo sapiens |
Tissue/cell | Keratinocyte |
Coordinate | chr10:115547870-115549290 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
NFE2L1 | MA0089.2 | chr10:115548596-115548611 | GAATGACTCAGCGTT | + | 6.21 | Nr2f6(var.2) | MA0728.1 | chr10:115548074-115548089 | GAGGTCAGGAGTTCA | + | 6.22 |
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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 |
GH10I113788 | chr10 | 115548188 | 115549279 |
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Enhancer Sequence | CTACATGGTG ATAGCAGGGT TCAGAAAGGA AGGAGATCGT GATGGAACAG AATGCCAACC 60 ATGACTAACA TGCAGAGAGT GCCTTCTATC TGCCGGGCAA TATTCAAACA CTCTACTGAC 120 TCCTATAAAA GCCCTGTGGG CCAGGTGCAG TGGCTCACAT CTGTAATCCC AGCACTTTGG 180 GAGGCCGAGG CAGGTGGATC ACTTGAGGTC AGGAGTTCAA GACCAGCTTG GCCAATATGG 240 AGAAACCCTG TCTCTACAAA AATACAAAAA TAAGCTGGGC GTCGTGGCGG GCATCTGTAA 300 TCCCACCTGC TCGGGAGTCT GAGGCAGGAG AATCGCTTGA GCTTGAACTC GGGAGGTGGA 360 GGTTGCGGTG AGCTGAGATA CTGCCACTAC GCTCCAGCCT GGGTGAGAGA GCGAGACCCT 420 CTCTCAAAAC AAAAACAAAA CAAAAAACAG CCCTGCGAGA CCAGGACTCT TATTGTCCCC 480 GGGTTTCGGA TGGGGAGACA AAGCACAGAG AAGATACATC GCTTGCTCAG GGCTATGGCT 540 AGTACCAGAC AGAGCCAGAA CTCAGACCAG AAAGACTGGC TTTGGAGACC ACAGGCGTCC 600 TGAAAGAGGA GCTGAAACTG AGCTCTGGAA GAGAATAATC CAGCAAGGGA CGGCGGTGCA 660 GACAGGATCA GACATGGAGC TCACTTTCCA AAAGTAAAAA CAGGGAACAT GTTGGAATGA 720 CTCATAGAAT GACTCAGCGT TTTTATACAT CTCTCATTTC AGTAACACGC ATTCATCTTT 780 GGGCCTATTG CCCAGAAGAA TCACAAAAGT GGTTCCTTTT GTGGTTCCGG GAGCCAGGGG 840 AATTCTGTGG CAGCTTCTGT TATGACTAGT AAACGCGTTT CATAACCCTC CTTTGAGTTG 900 GCCATCTGGC TCTATATTAT ACTCAAGTTA ATACAAAACT AATGCATACT TCTAGTGACA 960 AAGGCATTAG GCTAGTCCTC TGGACAGGAG ATAATAAAGA ATCCTTGGCT TTGTAGACCT 1020 CGTCATCAAG TGAAGGTAAT AAAAACATAC ACATAGATAC CTACAAGGCA AATATGATTA 1080 TCCTAAATCC TTTGTTAAAG TCACAACTCA ATGTTACAAA CACAAAAGGC TTAAAGACTA 1140 ATTCTATCTA GTTGGTTTGG AAAAAGCTTC AAGGGAGGGA TATATTTGGG GTGCAGAGAT 1200 GTAGTGGGAG GGATTTCATG TCTTGAAGAA TGAATAGGAT TCACTTAATA TTCTAGAACA 1260 GGTCAAACCC CCAGTGCACA GCCACCAGAA TGTAACTGGA GGGCCAAAGA AGTTCTCAAG 1320 CGTCCTGTAG AACTCCCTAA TCCCTGTCGG CTGTCACTGT CATCACTTTT CCAGCATCTT 1380 CTGGGTTCAG GGGACTGTCA GGCACTGGTG ATATTAACAG 1420
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