Tag | Content |
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EnhancerAtlas ID | HS095-04494 |
Organism | Homo sapiens |
Tissue/cell | HMEC |
Coordinate | chr10:115547850-115549260 |
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 | GAGGACAATG AACTATCAAA CTACATGGTG ATAGCAGGGT TCAGAAAGGA AGGAGATCGT 60 GATGGAACAG AATGCCAACC ATGACTAACA TGCAGAGAGT GCCTTCTATC TGCCGGGCAA 120 TATTCAAACA CTCTACTGAC TCCTATAAAA GCCCTGTGGG CCAGGTGCAG TGGCTCACAT 180 CTGTAATCCC AGCACTTTGG GAGGCCGAGG CAGGTGGATC ACTTGAGGTC AGGAGTTCAA 240 GACCAGCTTG GCCAATATGG AGAAACCCTG TCTCTACAAA AATACAAAAA TAAGCTGGGC 300 GTCGTGGCGG GCATCTGTAA TCCCACCTGC TCGGGAGTCT GAGGCAGGAG AATCGCTTGA 360 GCTTGAACTC GGGAGGTGGA GGTTGCGGTG AGCTGAGATA CTGCCACTAC GCTCCAGCCT 420 GGGTGAGAGA GCGAGACCCT CTCTCAAAAC AAAAACAAAA CAAAAAACAG CCCTGCGAGA 480 CCAGGACTCT TATTGTCCCC GGGTTTCGGA TGGGGAGACA AAGCACAGAG AAGATACATC 540 GCTTGCTCAG GGCTATGGCT AGTACCAGAC AGAGCCAGAA CTCAGACCAG AAAGACTGGC 600 TTTGGAGACC ACAGGCGTCC TGAAAGAGGA GCTGAAACTG AGCTCTGGAA GAGAATAATC 660 CAGCAAGGGA CGGCGGTGCA GACAGGATCA GACATGGAGC TCACTTTCCA AAAGTAAAAA 720 CAGGGAACAT GTTGGAATGA CTCATAGAAT GACTCAGCGT TTTTATACAT CTCTCATTTC 780 AGTAACACGC ATTCATCTTT GGGCCTATTG CCCAGAAGAA TCACAAAAGT GGTTCCTTTT 840 GTGGTTCCGG GAGCCAGGGG AATTCTGTGG CAGCTTCTGT TATGACTAGT AAACGCGTTT 900 CATAACCCTC CTTTGAGTTG GCCATCTGGC TCTATATTAT ACTCAAGTTA ATACAAAACT 960 AATGCATACT TCTAGTGACA AAGGCATTAG GCTAGTCCTC TGGACAGGAG ATAATAAAGA 1020 ATCCTTGGCT TTGTAGACCT CGTCATCAAG TGAAGGTAAT AAAAACATAC ACATAGATAC 1080 CTACAAGGCA AATATGATTA TCCTAAATCC TTTGTTAAAG TCACAACTCA ATGTTACAAA 1140 CACAAAAGGC TTAAAGACTA ATTCTATCTA GTTGGTTTGG AAAAAGCTTC AAGGGAGGGA 1200 TATATTTGGG GTGCAGAGAT GTAGTGGGAG GGATTTCATG TCTTGAAGAA TGAATAGGAT 1260 TCACTTAATA TTCTAGAACA GGTCAAACCC CCAGTGCACA GCCACCAGAA TGTAACTGGA 1320 GGGCCAAAGA AGTTCTCAAG CGTCCTGTAG AACTCCCTAA TCCCTGTCGG CTGTCACTGT 1380 CATCACTTTT CCAGCATCTT CTGGGTTCAG 1410
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