| Tag | Content |
|---|
EnhancerAtlas ID | HS116-25844 |
Organism | Homo sapiens |
Tissue/cell | Left_ventricle |
Coordinate | chr4:57623280-57624850 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| SCRT2 | MA0744.1 | chr4:57624777-57624790 | ACGCAACAGGTGA | + | 6.22 |
|
| | 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 |
| GH04I056757 | chr4 | 57622837 | 57625432 |
|
Enhancer Sequence | TAAGATGAGA AGCAGAGAGG GCTAGAATCC TGCATTATTA GCAAGAGGGG ACAAGGAATA 60
CCCTTCGACC TTACTATTTG ACAGCTTTGT ACATGAAAAA ACTAATACAC AAAGCCCGTG 120
GTTGGCTTGA AGGAGGTAAG GAAGAGACTC TCTGTATCCT CTGGTTGTGA CTGTTCAACC 180
CATCCCAAGG GATGTAACTC CCAGTGCAGT GTGCTCTGAC TCACAGGGAA CAGCCAGCTT 240
AGTGCCTGTC AAGGCCTTCC CTCCCAAACC CCAGGCAGCT GGATTCTGCA GGCTGGTTCT 300
GGATCTGGGT GGTACTTTCC AGGCCCAGCC TGACACCAGT TTTAAAGGCC ACCCCGGGTA 360
TCTATGGGCT CTGGGAGACG TAGGATGGAA ATGACCCAAG GCCTGGGATA TACACCAGGC 420
CACAGCCAGA ATGCAGGCAG TTCAGGCAGC ATGTGTAGTA AATACACACT AAGATGTAAT 480
CCAGCAGGCC CCCCTGTACC ACGCCCCACA GGTGGCACCA GCGTATAAAA CAACCTGACA 540
GCTACGGGCT GGAGAAGAGA CACAGGCTGG CCTGGACAGG GTGTAGACAT TGTTAAACAC 600
TTAGTTGAGT ATCTGTGGGC AAGTCTTGAG ATCGCTAAGT AGAATCTGAG CTTTGTTTCT 660
TTGGTTTTTG GTCTTTTTTT TTTTTAAAGA AAGTACAAAT ACAAATTATG TGATTCCCTT 720
TTCTCCTCTT AGACTGCCTT GCTCATCTGC TGCTTGGTCG AAGCCATTTG CTCCTCCCCC 780
ACACGCTTTG CTCATCAAGC AACCAGAGCG TTCCTGCCAC CTGAGTCATT CTGTCCTGTG 840
CTGCTCTGTC ACCCTGTGAG TGTGAAGCCC CTGCTCCGGC CCTCCAGGAG GAAGGAGGCA 900
GAGTGAAGCC AGGCATCTCT GGAGCCATGC GTTTGGCTTC AAAGTAGGAG GGACTGGGAC 960
TCTTAGGATG GAAAGTCTAG GGTAGGAGGG CAGGAGCTTG ACTTTCAGCA ATAAGGTAGG 1020
GAGGGAGGTG GTTTTACTGC AGAGGACTGG GTTTTACTTG CTATGAGCCT GTTTAGCTCT 1080
TTAAGAGCTG AACCTAAGTG TTTTTTTTTA AATATAGTTA TTTATTTTGG GCTCCAGCTT 1140
CCTGCAGTTG CGGTTTCTGT CAGACTAGTT TGTTAAAAAA AGCACTTAGA ACACATACCA 1200
GAGGACAGGA AGAAAGCAAA ATACTGGCAC TTTTGAAAAG TGTTGTTTTT ACATGACTTG 1260
AATTTTAGTT CCTACTCAGG GTTAAAGGAA GTTCTCTTCC GAATAAAGAG TGCCTGTTGG 1320
GTGAGAGAGG ATTTGCAACT GGAGTTGGAG ATTCTGTGTC ATTGGAGACA TTTGTTCGTA 1380
TGCATGGGCT TTAAAACACC AAGAAAAAAT ATACAGGAGA GTCCTTCCTT TTGTTATATA 1440
CTAGCTGTGT TCCTGAAAAC GTATATGAAA ACATTAAAAA ACTGATCCCT ATTCAGAACG 1500
CAACAGGTGA GCTCACTAAA GGGCTCTTAC CAGAAAGTCT TATAAATTGA GGCACTTGAA 1560
GGGCTGGGAC 1570
|
