| Tag | Content |
|---|
EnhancerAtlas ID | HS092-17110 |
Organism | Homo sapiens |
Tissue/cell | HFF |
Coordinate | chr14:105720940-105722340 |
Target genes | | Number: 18 | 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 | CAGGCTGGAG TGCAATGGCG CAATCGTGAC TCACTGCAAC CTCCACCTCA AGGGTTCAAG 60
CGATTCTCCT GTCTCACCCT CCTAAGTAGC TGGGATTATA GGCATCCGCC ACAACGCTCA 120
GCTAATTTTT GTATTTTTAG TAGAGACGGG GTTTCACCAT GTTGGCCAGG CTGGTCTTGA 180
ACTCCTGACC TCAGGTGATC TGCCTGCCTC AGCCTCCCAA AGTGCGGGGA TTACAGGTGT 240
GAGCCACCGC GCCCGGCCTA AATACATGCA GTTCTTTACA GAGTTGCTAC CATGTATGAG 300
GACCATTTAT TGGAAATTCT CTTGCTAACA GTCTAACTGT GGCTGCTCCT TGAGGGCAGG 360
TCAGGGTGGG GCACAGCCAG CTGCCCCCCC CATCTCTCTT CCTGGGCAGC AGGTGGATTC 420
TGCCTGCAGA CTGCCCTCGT GGGTGTCTGA TGAGCTGTGT GCCCAGGCCA GTGAACAACC 480
TGGGTCTGCC CTAAGGCAGG GATCAAGAGG GAGACTCCAT GAGCTCGCCA TGGGACCATC 540
TGAGTCCCCA GGAGCCTGAC CACTTCCGGA GCAGCTGCCC TGGCCCTGGC CCTCATACTC 600
ATCTTCCCTG GGAAGTCGTG GGGTTGGAAC CAGGGTCATG TGGTTTTGCC CTGCACTGAG 660
CAGAGAGCAT CTGAAATGTG GACTTGCTGG ATTATCACAA TTCCAGCAGA CTATTTTTAG 720
CTTGACCACA AAATGTTTCA GCAGTAGCTT CTGAGTTGCC ATTTATAAAG ACAGCTGGGA 780
GGACAAGGAC CCCAGATGCC ACCTGACACG GGCAGAAGCC TAACTGTGGG CTGCTGCCAA 840
AGGCGGAAAG CCCTTGAGGA CCAGAGGTGG CAGCACAGCC TGTGGGTGCC CAGAACCCCT 900
GTGGGCACCT GGATCTGGAC AGAGCTCCCT TTGAGGAGTG AAATCTACAT GAATTCTGCA 960
CTGTGGTCAC AACTGTTTTC AATATTTCTG AGTCCTCAGC AGCATGGTCA CCAAGGACCT 1020
GTGGTGCAGC CCCCAGCACC GTCCCTGCAG AGCCTCGGTG CCCCCACCCT GTATCCTGTC 1080
TGCACAGGGG TCCCTGGGGT TGGTCTTTCC ACTCTGTCAC TTTGTTCAGT CATGTGGAAA 1140
GAGAGATGTA ACTGAAAGTG CTTTCTGTGG TACCCAGAAA GTGAGTGTCT CCAAACAGAC 1200
TGTAATATAA GATTTTTCTA CAATTTAAAA TGCATGCAAG AGGCCAGGTA TGGTTGTTCA 1260
TGCCTGTGAC CCCAGTACTT AGGGAGGCCT TGGTGGGAGG GTTGCTTGAG CTCAGGAGTT 1320
CAAGAGCAGC CTGGGCAACA TAGCAAGACC CCGTCTCTAC TAAAAATACA AAATAGCCGA 1380
GCATGGTGGT GGGCACCTGT 1400
|
