Tag | Content |
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EnhancerAtlas ID | HS095-09907 |
Organism | Homo sapiens |
Tissue/cell | HMEC |
Coordinate | chr15:43182140-43183540 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Nr2f6(var.2) | MA0728.1 | chr15:43183290-43183305 | TGAACTCCTGACCTC | - | 6.22 | Stat4 | MA0518.1 | chr15:43182987-43183001 | CTTCCAGGAAAAGA | + | 6.38 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr15 | 43182504 | 43183140 | chr15 | 43182414 | 43182477 |
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| Number: 1 | ID | Chromosome | Start | End |
GH15I042889 | chr15 | 43181860 | 43184238 |
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Enhancer Sequence | ATATAAGAAG ACAGGAATGT CAGGCCTCTG AGCCCAAGCT ATGCCACCAT ATCTCCTGTG 60 ACCTGCACGT ATATATCCAG ATGGCCTGAA GCAACTGAAG ATCCACAAAA GAAGTGAAAA 120 TTGCCTTAGA TGATGACATT CCACCATTGT GATTTGTTTC TCCCCCACCC TTAAGAAGGT 180 TCTTTGTAAT TCTCCCCACC CTTGAGAATG TACTTTGTGA GATCCACCCC CTGCCTGCAA 240 AACATTGCTC CTAACTCCAC CACCTATCCC AAAACCTGTA AGAACTAATG ATAATCCCAC 300 AACCCTTGCT GACTCTCTTT TCGGACTCAG CCTACCTGCA CCCAGGTGAA ATAAACAGCC 360 TTGTTGCTCA CACAAACCTG TTTGGTGGCC TCTTCATATG GACATGAGAC AATAAGCATA 420 TCCATATGTT GTGAGGGTAG TGTATCCTAA CTTCATGAGG AAAGAAACTC CTGCTCTGAG 480 GATCCTTCCA GACTTTGCCC TATGTATCTC TTCACCTGTA TCCTCATTTA TATCCTTATT 540 AGATAATAAA CCAGTAAGCA TAAATGAAGT GTTTTCCTGA GTTCTGAGAG CCATTCTAGC 600 AAATTGCACT TCTCTGTCAT TTGCCAGAAG TATTCAGTAT AGTAGTAAGA ACAGTTTATT 660 TTTTCCTATC TTACATTTTT GTGTCAGAGG ATTGGTATTC ATTTCCAAAT TCCTGGCAGT 720 GCTTGGAATT TCCTAAGTGA TATGAATGCC TTTGTTATGC TAATGAAGTG ACTCCAAGCT 780 TCAGGATGGG GGCTGTCACC TGAAAGCATA TGACTACATG ACTAGAACCT TCATCTCCAC 840 CTCCCAACTT CCAGGAAAAG AGTTACTAGT GATTGAGTTC AATCACATGG CCAATGATTT 900 AATCAACCAT GCCTACGTAA TAAGCTCTTT TTGTTTGTTT TTTGAGATGG AGTCTCACTC 960 CTTTTGCCCA GGATGGAGTG CACTGGCGCA ATCTTGGCTC ACTGCAACCT CTGCCTCCAG 1020 GGTTCAAGCG ATTCTCCTGC CTCAGCCTTG TGAGTAGCTG GGATTACAGG TGTGCACCAC 1080 CACGCCCGGC TAATTTTTTT GTATTTCTGG TAGAGACGGG GGGTTTTACC ATGTTTGGCC 1140 AGGCTGGTCT TGAACTCCTG ACCTCAGGTG ATCCACCCAC CTCGGCCTCC CAAAGTGCTG 1200 GGATTACAGG CGTGAGCCAC CATGCCCGAC TTTTTTTTTT TTTTTTTTTT TTAAGAGATG 1260 GGGTCTCACT GTCGCCCCGG CTGGAGTGCA GTGGTGCAAA CATAGCTCAT TGCAGCCTCA 1320 AACTCCTGGG CTCAAGCAGT ACTCCCATCT CAGCTTCCCA AGTAGCTAGA CTACATGCAT 1380 GTGCCACCAC ACCCAGCTCA 1400
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