| Tag | Content |
|---|
EnhancerAtlas ID | HS094-42070 |
Organism | Homo sapiens |
Tissue/cell | hMADS-3 |
Coordinate | chr8:144300630-144301400 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Nr2f6(var.2) | MA0728.1 | chr8:144301184-144301199 | GAGGTCAGAAGTTCA | + | 6.38 | | Nr5a2 | MA0505.1 | chr8:144300732-144300747 | GAGCTCAAGGTCACA | + | 6.38 | | RARA | MA0729.1 | chr8:144301184-144301202 | GAGGTCAGAAGTTCACGT | + | 7.2 |
|
| | 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 |
| GH08I143217 | chr8 | 144299859 | 144303931 |
|
Enhancer Sequence | CAGGCTCTGA GCAGGAAGAG AGGGTATCGT GCTTAGCTGT CTACGGTGGG CCCTGTCACA 60
GCCCCCCGAG GTACGAAAGC CTGCAGCTGC GACATGAGGC TCGAGCTCAA GGTCACACAG 120
CTGGGCGGTG CAGATCCAGG ATCCAGTCCC CGGGCTTCCT GCCAACCGCA CCCAGCTTCC 180
CAGAGGTGTC CCAGGCTCCA GGACGCCTCA GCTGGGGAGG AGCTGGATGT CAGCCAAGAG 240
CCAGCCAGAT TCCCAGGCCA AGTCGAGTCT GAGCCAGGCA AGTCAGCGGT GCCAACGGGC 300
GGATGGTCAC AGCCAAGACA CCCTGGGCCC CGTCTCAGAG CCCAACGCAT GCTGTCAGTC 360
TCAAGAGTGA ACATAGAGGG ACCTCCCTTT CTCATCCAGC CCAGCAGCAG GGAGACTGGG 420
GGCTGGGGGG CTGGGCAGGG AGGGGGCAGG GCCCTGGCCC AAGAACCCAT GTCCCTCTGT 480
ACCAGTTTCC CAGGGCTGCC ATAACAAATC ACCACGAACC TAGTGACTTA ACACAAGTTC 540
ATGCTGTGGC TCTGGAGGTC AGAAGTTCAC GTCAGGGCTC TGGCTGGGCT GCGTTTTCTT 600
GGGAGAGAAT CCACCCCCGC CCTCTCAGCT TCAAGAGGCC ACCTGCTCTC CTTGGCTCAT 660
GGCCCTTCCT CCACCTTCGA AGCCGCTCCA ACCACTGCTC CCTCACCAGC TTCCCGAGTC 720
AGCTCTCCCT CGGCCTCCTT CTTACAGGGA TCCTGTGACC ACAGTTAGGA 770
|
