| Tag | Content |
|---|
EnhancerAtlas ID | HS116-25428 |
Organism | Homo sapiens |
Tissue/cell | Left_ventricle |
Coordinate | chr4:714490-716030 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ESR2 | MA0258.2 | chr4:715358-715373 | GGGTCACCCTGCCCC | + | 6.83 | | RREB1 | MA0073.1 | chr4:715548-715568 | GGGAGGTGGATGGGTTGGGT | - | 6.26 | | RREB1 | MA0073.1 | chr4:715753-715773 | GGGAGGTGGATGGGTTGGGT | - | 6.26 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_01023 | chr4:713657-716138 | Adrenal_Gland |
|
| | 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 |
| GH04I000720 | chr4 | 714327 | 715859 |
|
Enhancer Sequence | TGGACCCGGC GTGGACGGGC GGTGACGTGC GTGTGGACCC GGCGTGGACG CAGCCCCGAC 60
GTGAATGGAT GTGGTTCCGA CGTGACTGCG CTGGCATGGG AAGCAGAGGG TGAGGCTCGG 120
CTCTGCTGTC AGGAGGACAT GTCAGACTTC TGTCTCTAAG ATACTGCTCA GACTTGTGTG 180
GAGGGTGAAT TAGTGCGAGG GCGGCTTGGA GAAGCCTGTC CTGGGCGGGT TTCACCACTT 240
GGACGGGAGC TCTGGCATGG TCCAGGGAGT GGCCGAGGAC AGCAAGGAGG AGATGACCCC 300
ATGGGCAAGC AGGAGCTCAG ATGGGAGGCA TGGAGCAGAC GGGACTCCAC GTGGCACCAC 360
CCCTCCCACC TGGGCTGGGC ACCCATGAGG CTGAGGACCC TGGGGAGGGA ACGCTGCTTG 420
TCGGGCGGTG GTGACGATTT CATGGATGTT TGTGAAACCA ACCTCACTGC CCCATTACAA 480
CAGTGCGGGC CCTGATTCTC ATGGTTCCCC AGTGAGGCTG TTCCACGGTG GCACAGGACA 540
CGCCTGCAGC TTTGTGCCTG TGAATCTCAG GAGCTGTTTT CTGGAAAGTT CCATAACTCA 600
GCAAAACTGA CTCACAAACA ACAGAAACTT CAAGGCTGTC CTAAGATATG GGTGGCAGAA 660
GAAAATGTGC CCCAGGCATG GGCTTGTGAT GCCGGCTCTT CCTCCTGGCA GAGCTCCCCA 720
GAGGAAGGCT GGGCTGGGCA GTCAGCCAGA CGGGAAAGGG GGCTGAGGCG TCCAGGCTGC 780
AGAGGGTGCC GGGGTGGAGA GCGGAAGAGA GAGGGAGTCG GTGCCTTAGG AGGCTGCGGG 840
CGAGGCGAGG GCAGAGTGCA CTCGCTGGGG GTCACCCTGC CCCCCAGGAC TCCTTTCACA 900
GGACAGAGAA GCTCCTGGTG AGCGGGGCTG CTGAACGCAG GCCCCAGGGC CTGTAGGACC 960
CTTAGGGAGA CGGGTGGCTC TGCGTGTGGG TGTGGAGAGA GGCCTGTGGG AGACGGATGG 1020
ATGGGTGTCT CTGTGTATGG GCATGGGGAG GGGCCTGTGG GAGGTGGATG GGTTGGGTGG 1080
CTCTGTGTAT GGGCATGGGG AGGGGCCTGT GGGAGGTGGG TGGATGGGTG TCTCTGCATG 1140
TGGGTGTGGA AAGAGGCCTG TGGGAGACTG GTGGATGGGT GGCTCTGCGT GTGGGCGTGG 1200
AGAGAGGCCT GTGGGAGGTG GGTGGACATG TGTCGCTGCA TGTGGGTGTG GGGAGAGGCC 1260
TGTGGGAGGT GGATGGGTTG GGTGGCTCTG TGTGTGGGCG TGGAGAGGCC CGTGGCAGCT 1320
CCTTCGTTGC AGAAACCGCA TCGGAGCACA TCGCGTAGTG CAGGACACAC GGGGCGTGGG 1380
ACGGTGTCTG TGTGAGAGCA GCATCTGTGT GTATGCAGTG TTATCTAAGG ACACACCCAC 1440
AGACACGGAC ACGTCCTTAC GCAGAGAACA GCCGCTGCCT CTTAGTGTTC AGGATGATAC 1500
GTTTTTCCTT AATATCATCC TTCGCTTTGC ACATCATACT 1540
|
