| Tag | Content |
|---|
EnhancerAtlas ID | HS116-25497 |
Organism | Homo sapiens |
Tissue/cell | Left_ventricle |
Coordinate | chr4:6697240-6698610 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Nr5a2 | MA0505.1 | chr4:6698591-6698606 | GCTGACCTTGAGCCT | - | 6.9 | | Stat6 | MA0520.1 | chr4:6698282-6698297 | CATTTCCTGAGAACA | + | 7.08 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_32360 | chr4:6693831-6699251 | Gastric |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | CCCAGCCCCA TCCTGGGAAC TTGGGCTTGG GGCTCGGGGT GTTCTGATAA TGATCAAAGT 60
ATGAGAATTG AACCCATGAG GACTTTGATC CAAGATACTG GGGTGTGGGG AGGGGCAGGC 120
ACAGGTGTCC TGGGAACACA CTTTGAGAAG CAATGGCAAA GCTGGGGGTC CAGCTAATGT 180
GTTACATTAG AATCACCTCG GGGAGGCCCT GGGTGCCCTT CTCAGCCCTC CCTCCGGAGG 240
CTGCTGAAGC CCAGCAAAGC CGGAGTCAGA GAACAATGTC CGCCTGAGGG CAGGGCTGGG 300
CTGGGCTGGC CTTCTGGCCC TATCTGCTCC GTGCCCAACC CAGCGCCCCG CACAGTCGGA 360
GCTTTGTAAA TACGAGGTGA CTGTCTGCCT ACAAACTTTG TAAACATCAC TTGAAATGGC 420
CGCAGGGTAT TGTGACATGG CCATACCACT ATTTGTTTGC TATTGAATTT GTACTTCCCT 480
GCCTTACTTT TGCTATTGCA AACCATGCTG TCACTAAGGT CTTCATGCAC ACAGTTGTGT 540
CTTGGTCAGA TGATATGTTT CTACCAATTT TAATTGTGTT TCTTTCCACC TGGACACACA 600
GCTCTCTGGC CCAGGGCTGG GTCATCAGCA CACCCTGCTG CTGCTGTTCA GATCTGCATC 660
CTGGTCCCGC TTGGTCCCAC AGTGAGAACG CTTTGCTATC ACATGGGCAG GCTCTGAGAG 720
CCCTGCCGGC CTGGCCTTCT CAAAGAAGAC CTGAGAGCTT GGGACCCAAG CAGAGAGGAA 780
GAACAGGGCT CAGGGTGCTT GCTCCATGCT CGCTCCACAC CTGGGGCTCA ACCCTGGCTT 840
TCCCCGGCTC CCTGTGTGAC TTCAGGGCAG GTCCCTTGGG CCCTCTGGGC CTTATCATCT 900
TCATCTGTAA CAGGGCGATG CCTCTGCCGT GTCTGGTGGT GTTGAGGAGT TCCTGTTTGT 960
GTAAGCAGCT AGTTCAGTGC CAGCACGAGA TGGGAGGCCC ATGAAGTTAG CAGTGCACAA 1020
AAAATAGAGC AAAGACTGGA TGCATTTCCT GAGAACAACC ATCACTGTAA AGCACTTTAC 1080
AAATCCAAAG ACAACCCCCG GCAAAAACTC AAAATGAAAC TCCCTCTCGC AGAGCACAAT 1140
TCCAATTCGC TCTAAAAACA TTACAAGTTA GTTCATGTCA TGCCAGATAG CTGAAGGCAG 1200
CTCACAAGTT CTTAAGGCCA GGAATGCCAT GTGTCTGCTA TGCACAGCTG GCCCTGGCCC 1260
TGACAGCAAA GGTGACGCAG ATGTGGGTGC CCTGCTCCTG CCCAGCAGCA GTGCTTGGTG 1320
GAGGCTGAGG CCCTGCACAG GCACCCTCAC TGCTGACCTT GAGCCTCTCT 1370
|
