Tag | Content |
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EnhancerAtlas ID | HS065-01932 |
Organism | Homo sapiens |
Tissue/cell | GM18508 |
Coordinate | chr16:29961550-29962930 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Nr2f6(var.2) | MA0728.1 | chr16:29961551-29961566 | TGAACTTCTGACCTC | - | 6.38 | SREBF1 | MA0595.1 | chr16:29962191-29962201 | GTGGGGTGAT | - | 6.02 |
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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 |
GH16I029950 | chr16 | 29962140 | 29963681 |
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Enhancer Sequence | GTGAACTTCT GACCTCAGGT GATCCACCCA CCTCAGCTTC CCAAAGTGCT GGGATTACAG 60 GCGTGAGCCA CCACGCCTTC TAATGCATTC TTTAGTATGT CAATTGCATT TTCCAACTCT 120 AGAATTTCTG CTTATTTTTA GTTATTTCAA TCTCTTTGTT AAATTTATTG ATAGAATTCT 180 GAATTCCTTC TCTGTGTTAT TGTGAATTTC TTTGAGTTTC CTCAAAACGT CTTTTTTGAA 240 TTCTCTGTCT GAAAAGTCCC ATCTGTGTTT CTCCAGGATT AGTCCCTGGT GGCTTCTTTG 300 GTTCATTTGG TGAGGTCATG TTTTCCTGGA TGGTCTTGAT GCTTGTCAAT GTTCATCAGT 360 GTCTGCACAT TGAAGAGTTA GGTATTTATT GTAGCCTTTG CAGTCTGGGC TTGTTTGTGC 420 CCATCTTTTT TGGGAAGGCT TTCCAGGTAT CCAAAAAGAC TTGAGCTCCA AGCCCAATAA 480 CACTGTGGTT CTTGTGGACT CATATAAGTA CCACCTTGGT GGTCCTAGAT AAGATCCAGA 540 TGAATTCTCT GATTACTAGG CAGAGACTCT TGTTCTCTTT CCTTACTGTC TCCCAAATAA 600 ATGGAGTCTC TGTCTCTTTG CTGAGCTTCC TGGAGCTAGG GGTGGGGTGA TGCAAGCCTT 660 CTTATGACCA CCACCATTAG GACTGTGCTG GGTCATACCT GAAGCCAGCA CAGCAGTGGG 720 TCTCACCCAA GGCCCACTGT AACCACTACC CGAATACCAT CTATGTTCAC TCAAGGCCCT 780 AGGGCTCTAC AATCAGCAGC TAGGGCCACC AGTCTGATTT CTATCTTTCC CTTCAGGGCA 840 GCGAGTTCCT CCAGGTCCTG GGAGGGTCCA GAGATAATGT CTGGGAGCCA CGGATTAGAG 900 TCAAAAACCT TAGAAATCTA CCTGGTGTTC TATTCTACTG CAGCTAAGCT GGGACTCAAA 960 CCACAAGACA AAGTGCCTCC CACTCTACCT TCCCCTTTCC ATGGACAGAG GACAGAGGAG 1020 CCTCTCCCAG TGGCCACTAC CACCACTGGC CTGCAGAGAG TTCTGAACAC TCACTTAAAG 1080 CCCAAGGCCT CTTCAAGTCA ACTTGTGGTG AATGCTCTCA GGCCTGGGAC TCACCCTTTA 1140 GGACAGTGGG TCCCCCTCTG GCCCACAGCA GGTCCAAAAA TGTTGTCCAA GAGCTTAGGT 1200 CTGGACTCGG GGACCCCAAA AATCTGCTTG GTACCCTACC CCACTGTGTC CGAGCTGGTA 1260 TCTAAGGGGC AAGACAAAGT TCCCTTTACT CTTCTCTCCA CTTTTCTCAA GCAGTAGTCT 1320 TTCACCAGGG CCACCACAGC TGGTAATGTG CTGGGCCCTA CCTGAAGCCA GCACAACTCA 1380
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