| Tag | Content |
|---|
EnhancerAtlas ID | HS098-18647 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr14:105721050-105722310 |
Target genes | | Number: 11 | Name | Ensembl ID |
|
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 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH14I105254 | chr14 | 105721182 | 105722094 |
|
Enhancer Sequence | ACAACGCTCA GCTAATTTTT GTATTTTTAG TAGAGACGGG GTTTCACCAT GTTGGCCAGG 60
CTGGTCTTGA ACTCCTGACC TCAGGTGATC TGCCTGCCTC AGCCTCCCAA AGTGCGGGGA 120
TTACAGGTGT GAGCCACCGC GCCCGGCCTA AATACATGCA GTTCTTTACA GAGTTGCTAC 180
CATGTATGAG GACCATTTAT TGGAAATTCT CTTGCTAACA GTCTAACTGT GGCTGCTCCT 240
TGAGGGCAGG TCAGGGTGGG GCACAGCCAG CTGCCCCCCC CATCTCTCTT CCTGGGCAGC 300
AGGTGGATTC TGCCTGCAGA CTGCCCTCGT GGGTGTCTGA TGAGCTGTGT GCCCAGGCCA 360
GTGAACAACC TGGGTCTGCC CTAAGGCAGG GATCAAGAGG GAGACTCCAT GAGCTCGCCA 420
TGGGACCATC TGAGTCCCCA GGAGCCTGAC CACTTCCGGA GCAGCTGCCC TGGCCCTGGC 480
CCTCATACTC ATCTTCCCTG GGAAGTCGTG GGGTTGGAAC CAGGGTCATG TGGTTTTGCC 540
CTGCACTGAG CAGAGAGCAT CTGAAATGTG GACTTGCTGG ATTATCACAA TTCCAGCAGA 600
CTATTTTTAG CTTGACCACA AAATGTTTCA GCAGTAGCTT CTGAGTTGCC ATTTATAAAG 660
ACAGCTGGGA GGACAAGGAC CCCAGATGCC ACCTGACACG GGCAGAAGCC TAACTGTGGG 720
CTGCTGCCAA AGGCGGAAAG CCCTTGAGGA CCAGAGGTGG CAGCACAGCC TGTGGGTGCC 780
CAGAACCCCT GTGGGCACCT GGATCTGGAC AGAGCTCCCT TTGAGGAGTG AAATCTACAT 840
GAATTCTGCA CTGTGGTCAC AACTGTTTTC AATATTTCTG AGTCCTCAGC AGCATGGTCA 900
CCAAGGACCT GTGGTGCAGC CCCCAGCACC GTCCCTGCAG AGCCTCGGTG CCCCCACCCT 960
GTATCCTGTC TGCACAGGGG TCCCTGGGGT TGGTCTTTCC ACTCTGTCAC TTTGTTCAGT 1020
CATGTGGAAA GAGAGATGTA ACTGAAAGTG CTTTCTGTGG TACCCAGAAA GTGAGTGTCT 1080
CCAAACAGAC TGTAATATAA GATTTTTCTA CAATTTAAAA TGCATGCAAG AGGCCAGGTA 1140
TGGTTGTTCA TGCCTGTGAC CCCAGTACTT AGGGAGGCCT TGGTGGGAGG GTTGCTTGAG 1200
CTCAGGAGTT CAAGAGCAGC CTGGGCAACA TAGCAAGACC CCGTCTCTAC TAAAAATACA 1260
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