Tag | Content |
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EnhancerAtlas ID | HS139-17787 |
Organism | Homo sapiens |
Tissue/cell | Myotube |
Coordinate | chr14:105720740-105722520 |
Target genes | Number: 18 | Name | Ensembl ID |
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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 | Zfx | MA0146.2 | chr14:105720837-105720851 | CCCGCCTCGGCCTC | + | 6.01 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr14 | 105720866 | 105721019 | chr14 | 105721279 | 105722125 |
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| Number: 1 | ID | Chromosome | Start | End |
GH14I105254 | chr14 | 105721182 | 105722094 |
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Enhancer Sequence | CCACCACCAC GCCCAGCTAA TTTTTTTGTG TTTTTAGTAG AGATGGAGTT TCACCGCGTT 60 AGACAGGATG GTCTCGATCT CCAGACCTCC TGATCTGCCC GCCTCGGCCT CCCAAAGTGC 120 TGGGATTACA GGAGTGAGCC ACCGCACCTG GCCGCAGTTT TTTGTTTGTT TTCTTGAGAC 180 AGAGTTTCAC TCTTGTTGCC CAGGCTGGAG TGCAATGGCG CAATCGTGAC TCACTGCAAC 240 CTCCACCTCA AGGGTTCAAG CGATTCTCCT GTCTCACCCT CCTAAGTAGC TGGGATTATA 300 GGCATCCGCC ACAACGCTCA GCTAATTTTT GTATTTTTAG TAGAGACGGG GTTTCACCAT 360 GTTGGCCAGG CTGGTCTTGA ACTCCTGACC TCAGGTGATC TGCCTGCCTC AGCCTCCCAA 420 AGTGCGGGGA TTACAGGTGT GAGCCACCGC GCCCGGCCTA AATACATGCA GTTCTTTACA 480 GAGTTGCTAC CATGTATGAG GACCATTTAT TGGAAATTCT CTTGCTAACA GTCTAACTGT 540 GGCTGCTCCT TGAGGGCAGG TCAGGGTGGG GCACAGCCAG CTGCCCCCCC CATCTCTCTT 600 CCTGGGCAGC AGGTGGATTC TGCCTGCAGA CTGCCCTCGT GGGTGTCTGA TGAGCTGTGT 660 GCCCAGGCCA GTGAACAACC TGGGTCTGCC CTAAGGCAGG GATCAAGAGG GAGACTCCAT 720 GAGCTCGCCA TGGGACCATC TGAGTCCCCA GGAGCCTGAC CACTTCCGGA GCAGCTGCCC 780 TGGCCCTGGC CCTCATACTC ATCTTCCCTG GGAAGTCGTG GGGTTGGAAC CAGGGTCATG 840 TGGTTTTGCC CTGCACTGAG CAGAGAGCAT CTGAAATGTG GACTTGCTGG ATTATCACAA 900 TTCCAGCAGA CTATTTTTAG CTTGACCACA AAATGTTTCA GCAGTAGCTT CTGAGTTGCC 960 ATTTATAAAG ACAGCTGGGA GGACAAGGAC CCCAGATGCC ACCTGACACG GGCAGAAGCC 1020 TAACTGTGGG CTGCTGCCAA AGGCGGAAAG CCCTTGAGGA CCAGAGGTGG CAGCACAGCC 1080 TGTGGGTGCC CAGAACCCCT GTGGGCACCT GGATCTGGAC AGAGCTCCCT TTGAGGAGTG 1140 AAATCTACAT GAATTCTGCA CTGTGGTCAC AACTGTTTTC AATATTTCTG AGTCCTCAGC 1200 AGCATGGTCA CCAAGGACCT GTGGTGCAGC CCCCAGCACC GTCCCTGCAG AGCCTCGGTG 1260 CCCCCACCCT GTATCCTGTC TGCACAGGGG TCCCTGGGGT TGGTCTTTCC ACTCTGTCAC 1320 TTTGTTCAGT CATGTGGAAA GAGAGATGTA ACTGAAAGTG CTTTCTGTGG TACCCAGAAA 1380 GTGAGTGTCT CCAAACAGAC TGTAATATAA GATTTTTCTA CAATTTAAAA TGCATGCAAG 1440 AGGCCAGGTA TGGTTGTTCA TGCCTGTGAC CCCAGTACTT AGGGAGGCCT TGGTGGGAGG 1500 GTTGCTTGAG CTCAGGAGTT CAAGAGCAGC CTGGGCAACA TAGCAAGACC CCGTCTCTAC 1560 TAAAAATACA AAATAGCCGA GCATGGTGGT GGGCACCTGT GGTCCCAGCT ACTTGGGAGG 1620 CTGAGGTGGG AGGATTGCTT GAGCCCAGGA GGCAGAGGTT GCAGTAAGCT GAGATCACGC 1680 CACTGCACTC CAGCCTGGGT GACAGAGCGA GACTCCATCT CATAAATAAA TAAATAAATA 1740 AAATGCAAGG TCAAAAGAAA TAATCTCCTA TACCAAACTA 1780
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