Tag | Content |
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EnhancerAtlas ID | HS184-15651 |
Organism | Homo sapiens |
Tissue/cell | T47D |
Coordinate | chr19:47234190-47235620 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
NFE2L1 | MA0089.2 | chr19:47234457-47234472 | CACTGACTCAGCAGT | + | 6.16 | ZNF263 | MA0528.1 | chr19:47235013-47235034 | GCTTCCTCCTCCTGTTCCTCC | - | 6.66 | ZNF263 | MA0528.1 | chr19:47235004-47235025 | TCTTTCTCAGCTTCCTCCTCC | - | 6.86 | ZNF263 | MA0528.1 | chr19:47235016-47235037 | TCCTCCTCCTGTTCCTCCCTC | - | 7.77 |
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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 |
GH19I046727 | chr19 | 47231173 | 47238057 |
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Enhancer Sequence | GAAGGTGCCC TCCCAGGCTT GGTGGCCAGA GCCCAGACCC AGCTAACCCC CTAACCCCTG 60 AGCAGCCTTG ACTCTGGTCA CACACAGAGC CCCAACCCCA GCCTCTGCCC AACAAATGCT 120 CATTCCAACT GGAAGCCTCA CTCAGACCGC AAACGGGGCC CAGCTCCTCA ATGACCGCCG 180 ACCTGAGTTT CAGAGGGCCA GCCCCCAACC CTGGTCACAA ATCTCCATCC TGTGCTGAGT 240 CAGAAGGAAA GCTGGATGAG AAAGTGCCAC TGACTCAGCA GTCCCCATTC CCACAGCCCA 300 GTCAGACCAC AAGGGCAGGT CAGGCAGGAG GCAAACACGC CCTGCAGGAA AGAGGAACCG 360 GCCATTCTAC AAATGCTCTG GGAGGCGCCG AAAGCCAGCC AGCCTCGCGC AAGCAGGGGC 420 GCCGGCGATC CCTGCTACCC AGGAGCCTGC ACTATCCCCA GCAACAGATG GCACTCCTCC 480 TTCCACCTCC TGGCTTCCAA CTTCATGACA AGTTATAGCA GAGGAGGTAC TGACCCAGCC 540 TGACTGCGGG AGAAGGCAGG GTGCAATTCC AAGTGCAGAT CGACGAAAAC GTCCCCCCTT 600 TCTGCCATCA GGTTGATGCC CTGGAGGTCT TGTCAACTGC CAGTTACCAA CGGGTGCAGA 660 GGTCACTGCA GATGTACCCT CTCGCCTCAC GGCTGCCATC ACCAGAGCTC CACTCCATCC 720 TCAGAACACT CGCTGCACTT GCAGCGGGAC ACAGGACTCC ATTCTCACCG GCCTTCCTCC 780 CACAACGACA CTGACACGCC GCACAGGCTC AGCCTCTTTC TCAGCTTCCT CCTCCTGTTC 840 CTCCCTCCAG CCTCTAAGTG GGAGAGCACC CGGGCAGTCC CCAGATCTCT TCTCTGCGTC 900 ATCTACACTC ACTCCTGCAG GCACTGCAGA CGGCCATGGC TTTCCAAAGA ATGCCCATGT 960 GCTTGTTCAA CTAGACCTAT GTTTAGGGGC CAAATGCCCC GCAGCTCCAG ACGAGCTCTG 1020 CTTCTCCACA TGGGGGTAAA CAGGCCCCTC ACACTTCACA CAACCTCGGC GGCCCCCAGA 1080 ACTTCCACTC CCAGGCTTCC CCGTCTCAGG GGATGCTGCT CCAATGGCTC ACACCAAACC 1140 CTGGAGTCGC TCGTTTCTTT TCCTCTCCCC TTAGCTGCAG TCCTTCAGTG TCGACTGCCT 1200 GAAAGCCTCT GGGGAAGCTG ACACCTCTCG CCTCACCACC GCTAAAGTCC ATCAGCTCTG 1260 TCCCAGACAT CGAGCCATCT CCTAACTGGT CCGCCTGCCT CCTCTGTGAC CCTCCCACAC 1320 CTCTCCTTCT CAGAGTGGAT CAGGTACGTC AGATTATGTC ACCCCGCTGC TCGAAAGCAC 1380 TGGCTTCCCA CAACCCTGAG TCAAACTCAG ACTCTATCCC AGCCCAAGGC 1430
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