Tag | Content |
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EnhancerAtlas ID | HS086-08744 |
Organism | Homo sapiens |
Tissue/cell | HEK293 |
Coordinate | chr21:37431620-37432570 |
Target genes | Number: 11 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Nr2f6(var.2) | MA0728.1 | chr21:37431769-37431784 | 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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Enhancer Sequence | GATCGCGCTA CTGCACTCCA GCCTGGGCGA CAGAGCGAGG CTCCGTCTCA AAAAAATAAA 60 AAAATAAATA CATAAATAAA AATAAAATAA TGGCTGGGTA CAGTGGCTCA CGCCTGTAAA 120 ACCAGCACTT TGGGAGCCCG AGGCGGGCTG AGGTCAGGAG TTCAAGACCA GCCTGGCCAA 180 CATGGTGAAA CCCCGTCTCT ACTAAAAATA CAAAAATCAG CCGGGCGTGG TGGCAGGCAC 240 CTGTAATACC AGCTACTGGG GAGGCTGAGG CAGGAGAATC GCTTGATCTC AGGAGGCGGA 300 AGCTGCAGCT AGACGAGATC ACGCCACTGC ACTCCAACCT GGGCGACAGA GCGAGACTCT 360 GTCACAAAAA ATAAATTAAA AAAATAAAAA TAAAAAATAA ATCTACTTCT AAAACATACG 420 AGGGCAGAAA TGAGCAAGAG ACAAGAACTC CAGGCAATAT TAATACCGCA CTTCCGCAGT 480 ATAAGGTTCA TTATTTGACC TAACGAAAGT CGGCATGTCC AGCTCCAGAG GCGAACGGCG 540 GCTGGTTCGG TGCGGGTCCC AGCGCTCAGT CCACAGACCG CGCCGGGAAG TGTCCCCAAG 600 ACTCCCGGGC CCTCGCGCGA GCTGTCCACC ATCACCCTGC TGAGGACCAC GTGAAGCCCG 660 GTGACCGCCA CAGACACAGG CACCGTCCCC GCCCCCATAG TCCTCAAACT CTAGCCGTGA 720 GGCCGTCCTA CGGTCCGACA CACACCGCTC CCGCAGCCAT AGGCCAGCCA GGCGAGCATC 780 GGACCTCGGG CCTCAGGCTC CTCAGCTTTA CGCAGCGCGC CGGAGCAACA TGCGCTAAGT 840 GTAGGACTCC ACAAGATGAG AGGTTACTGC AGCGCACACG ATAATGCCTG CCCTGGAGGG 900 GACCTGCGAC CTAAACTCAG TTCTTTTTAC GCTGATGAAT GAAAGACTAA 950
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