Tag | Content |
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EnhancerAtlas ID | HS156-04121 |
Organism | Homo sapiens |
Tissue/cell | P493-6 |
Coordinate | chr15:56244670-56246480 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Nr2f6(var.2) | MA0728.1 | chr15:56245406-56245421 | TGAACTCCTGACCTC | - | 6.22 | Nr2f6(var.2) | MA0728.1 | chr15:56246146-56246161 | TGACCTCGTGACCCT | - | 6.36 |
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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 |
GH15I055952 | chr15 | 56244218 | 56245622 |
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Enhancer Sequence | TTCTCCTGTT TTCCTCGGGT ATCCAAAGTA CTCACCATTC TCCACGAAGT ACCCTCCAAA 60 CTAATCCAAA CTATCCTTCC CCCAACTCCA TTTCCTCATA CCACGTTACC TCTTAATTGG 120 CCAAACTCGA AGGCACCAGA ACACTCGCAA CATACTGGTA TTTATCAGAA TCCATCCTTA 180 CCCCTAACCT AGTGAGTCAG GAGTCCTCTT GTTTTGAGTC TCATCCCCCT TGTTCAGTTC 240 TCTGAACTTT GGAGCCTTGC GTCATCTGTT CTCACTGCTC TCTTTTAGAC CTTTGGCTTT 300 TTCTTTGATC TAGGTTTCTC TAGGCATATA AATGTTTTTA AACTCCTCCT CCCCTTGACT 360 TTCCCTCCCT TCTCCAGCAA AGCAAAATAC ATCCTTTTCT TCCATTCCCA GTCAAACCTT 420 TTCAGAGGCA GTTTTTAATA ATAAAAACAA GAACACTTAT ATAGCAATTA CTCAGTGCCA 480 GACACCACTG TAATCACGTT TCGTGTATTA ATTCTTTTTT TTTTTCTTTT TTTTTGAGAC 540 AGAGTCTTGC TCTGTTGCCC AGGCTGGAGT GCAGTGGTGC AGTCTTGGCT CACTGCAACC 600 TCTGCCTCCT GGGTTCATGC CATTCTCCTG CCTAAGCCTC CCGAGTAGCT GGGACTGCAG 660 GCGCACACCA CCACGCCCGG CTAATTTTTG TATTTTTAGT ACAGACAGGG CTTCACCATG 720 TTGGCCAGGA TGGTCTTGAA CTCCTGACCT CAGGTGATCC GCCCGCCTTG GCTCCCAAAG 780 TGCTGGGATT ACCCACGTGA GCCATAGCGC TGAGCCCGTA TATTAATTCT TTGAATCTCT 840 ATAACCACCT GTGAGGTAGG TACTATTCCT TTCTTTATTT CATACAGATC ACACAGCTAG 900 AAAGCGGACA GCCAGGATTG AAACTCCAGC ACCTGGCTCC AGAGGCCATA CTCTTCTTTT 960 TTTATCTTCT TTTTTGTTTT TTTTTTTGAG ATGAAGTCTC ACTCTGTAAT CCAGGCTGGA 1020 GTGCAGTGGC GCGATCTTGG CTCACTGCAG CTTCTGCCTC CTGGGTTCAA GCTATTCTCC 1080 TGCCACAGCC TCTCAAGTAG CTGGGATTAT AGGCACACGC CACCGCACCC AGCTAATTTT 1140 TGTATTTTTA GTAGAGACGC GGTTTTGCCA TCTTGGCCAG GCTGGTCTCA AACTCTTGAC 1200 CTCAGGTGAT CTGCCCGCCT TGGCCTCACA AAGTGCTGGG ATTACAGGCA TGAGCCAACA 1260 TGCCCGGCTT AAACTCTCTT GCTCTGTCGC CAGGCTGGAG TGCAATGGCA CGATCTCGGC 1320 TCACTGCAAC CTCCTCCTCC TGGGTTCAAG CAATTCTCCT GCCTCAGCCT CCTGAGTAGC 1380 TGGGACTACA GGCGCCTGCC ACCACGCTTG GCTAATGTTT TGTATTTTAA GTAGAGATTG 1440 GATTTCACCA AGTTGGCCAG GATGGTCTCA ATCTCTTGAC CTCGTGACCC TCCTGCCTCG 1500 GCCTCCCAGC CTATACTCTT AACGACTATA GCATACCACC TCCTTTTCTT CATTTCCTTA 1560 ATTCATGTTA CACTTCAAAA CCCTACAGTC TGGTTTCTGT CTCTTCCCTT TAGATCCACT 1620 CCTATGAAAA GGCTGTTGTA AAGTCATCAG TCTTGTTAAA GTAATCAACA TTTTCCAGAT 1680 ACTTCTTTTT TTGGCCCTCT TTATGTTTTT AGATACTACT GACCATTTTC TCTTTGAAAC 1740 ACTCATCTCA TTTTGCTTCT ACGACACATC TCTTCTAGTG CTCCTCATAC CACTCGAACT 1800 GTTCCTTCGG 1810
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