Tag | Content |
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EnhancerAtlas ID | HS170-01175 |
Organism | Homo sapiens |
Tissue/cell | RS4-11 |
Coordinate | chr14:105721100-105722520 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
MEF2B | MA0660.1 | chr14:105721649-105721661 | ACTATTTTTAGC | - | 6.11 | MEF2C | MA0497.1 | chr14:105721648-105721663 | GACTATTTTTAGCTT | - | 6.06 | Nr2f6(var.2) | MA0728.1 | chr14:105721117-105721132 | TGAACTCCTGACCTC | - | 6.22 | TFAP2C | MA0524.2 | chr14:105721426-105721438 | TGCCCTAAGGCA | - | 6.04 | TFAP2C | MA0524.2 | chr14:105721426-105721438 | TGCCCTAAGGCA | + | 6.32 | ZNF740 | MA0753.2 | chr14:105721320-105721333 | CTGCCCCCCCCAT | + | 6.36 |
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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 |
GH14I105254 | chr14 | 105721182 | 105722094 |
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Enhancer Sequence | GTTGGCCAGG CTGGTCTTGA ACTCCTGACC TCAGGTGATC TGCCTGCCTC AGCCTCCCAA 60 AGTGCGGGGA TTACAGGTGT GAGCCACCGC GCCCGGCCTA AATACATGCA GTTCTTTACA 120 GAGTTGCTAC CATGTATGAG GACCATTTAT TGGAAATTCT CTTGCTAACA GTCTAACTGT 180 GGCTGCTCCT TGAGGGCAGG TCAGGGTGGG GCACAGCCAG CTGCCCCCCC CATCTCTCTT 240 CCTGGGCAGC AGGTGGATTC TGCCTGCAGA CTGCCCTCGT GGGTGTCTGA TGAGCTGTGT 300 GCCCAGGCCA GTGAACAACC TGGGTCTGCC CTAAGGCAGG GATCAAGAGG GAGACTCCAT 360 GAGCTCGCCA TGGGACCATC TGAGTCCCCA GGAGCCTGAC CACTTCCGGA GCAGCTGCCC 420 TGGCCCTGGC CCTCATACTC ATCTTCCCTG GGAAGTCGTG GGGTTGGAAC CAGGGTCATG 480 TGGTTTTGCC CTGCACTGAG CAGAGAGCAT CTGAAATGTG GACTTGCTGG ATTATCACAA 540 TTCCAGCAGA CTATTTTTAG CTTGACCACA AAATGTTTCA GCAGTAGCTT CTGAGTTGCC 600 ATTTATAAAG ACAGCTGGGA GGACAAGGAC CCCAGATGCC ACCTGACACG GGCAGAAGCC 660 TAACTGTGGG CTGCTGCCAA AGGCGGAAAG CCCTTGAGGA CCAGAGGTGG CAGCACAGCC 720 TGTGGGTGCC CAGAACCCCT GTGGGCACCT GGATCTGGAC AGAGCTCCCT TTGAGGAGTG 780 AAATCTACAT GAATTCTGCA CTGTGGTCAC AACTGTTTTC AATATTTCTG AGTCCTCAGC 840 AGCATGGTCA CCAAGGACCT GTGGTGCAGC CCCCAGCACC GTCCCTGCAG AGCCTCGGTG 900 CCCCCACCCT GTATCCTGTC TGCACAGGGG TCCCTGGGGT TGGTCTTTCC ACTCTGTCAC 960 TTTGTTCAGT CATGTGGAAA GAGAGATGTA ACTGAAAGTG CTTTCTGTGG TACCCAGAAA 1020 GTGAGTGTCT CCAAACAGAC TGTAATATAA GATTTTTCTA CAATTTAAAA TGCATGCAAG 1080 AGGCCAGGTA TGGTTGTTCA TGCCTGTGAC CCCAGTACTT AGGGAGGCCT TGGTGGGAGG 1140 GTTGCTTGAG CTCAGGAGTT CAAGAGCAGC CTGGGCAACA TAGCAAGACC CCGTCTCTAC 1200 TAAAAATACA AAATAGCCGA GCATGGTGGT GGGCACCTGT GGTCCCAGCT ACTTGGGAGG 1260 CTGAGGTGGG AGGATTGCTT GAGCCCAGGA GGCAGAGGTT GCAGTAAGCT GAGATCACGC 1320 CACTGCACTC CAGCCTGGGT GACAGAGCGA GACTCCATCT CATAAATAAA TAAATAAATA 1380 AAATGCAAGG TCAAAAGAAA TAATCTCCTA TACCAAACTA 1420
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