Tag | Content |
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EnhancerAtlas ID | HS184-15820 | Organism | Homo sapiens | Tissue/cell | T47D | Coordinate | chr19:58883700-58884660 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Nr2f6(var.2) | MA0728.1 | chr19:58883816-58883831 | GAGGTCAAGAGATCG | + | 6 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | TAGGCGTGAG TCACCGCACC CAGCCGATAT CCATTTATTA AATGTCTCAG AGGGCCGGGT 60 GTGGTGGCTC ATGCCTGTAA TCCCAACACT TGGGGAGTCC GGGGGGGGCG GATCACGAGG 120 TCAAGAGATC GAGACCATCC TTGCCAACAT GGTGAGACGT CCTTGACCTG ATGTCACTTT 180 TTCTGTCTGT TTTGCAGATT TCTAACAGGC AGTTGCCCTG GGCCACCTGG TGGCCTGAAA 240 TAACTTGACC GGGAACTAAA AGGACTCACG AAGCATTTAA CCAAGACTCT ACATGTTGAC 300 TTTTCAGCCA AGGACACTTC AGAGCGACTG GCTGCAGTTC TCCAAAGGAA GCTGCTGCCA 360 GTTGCCCCTG GGGGGTTATT TCCTTCTTGG ACATCATGAC CACAATGGCA GAAATGCATT 420 GATGGCCAGC ACTCTGGGGA TGAATGTTTT TGAGTGGAAA TGAAACATAC CAAACTGGTT 480 AAAGACAAAA ATGCAGAGTT GGACAAGTTC TGCAGGTCAC GAAAGGCCTT TGAAGCAGCC 540 AGGCCCGGTT CCTGCTCTGC TGTATGGGAG GCTGCTGGCC TGAGCTGGAG AGCAGAAAGG 600 CCCAGTGCCA AGGGTTCAGC AAGTACCAGT CCCAGGCCAG GCATTTGCTA ATAAGCCAGG 660 GTGACAGTAA GGACAAGGGG ACTCTGGTGT GATGTGAGGT TTCTCAGCCT CACTTGTCAC 720 ACGTGATAAC TGCACAACCC TCCTGTCCCC TCCAGGCCTG TGTGAGACAG GAAAGGTGAG 780 GCTGCCTCTC CCTCTGCACC TTAAAGCCAC TCGGGGTCTG GGTTTTCCTG AGACTTCCCG 840 GAGCCAGATG CAGACTCCCA AAGGCGCCGA TCCTTCCTCG ATCTCCCTCC CTCAAGAGTG 900 GCACTAATCA GGTCTAATTT AGAGAAAATC CATCACCTCC CCCCACTGTG GGCTCTGCCA 960
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