| Tag | Content |
|---|
EnhancerAtlas ID | HS116-18607 |
Organism | Homo sapiens |
Tissue/cell | Left_ventricle |
Coordinate | chr2:66722730-66724040 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CREB1 | MA0018.3 | chr2:66723342-66723354 | TGTGACGTCATC | + | 6.02 | | CREB1 | MA0018.3 | chr2:66723342-66723354 | TGTGACGTCATC | - | 6.02 | | JDP2(var.2) | MA0656.1 | chr2:66723342-66723354 | TGTGACGTCATC | - | 6.32 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_60232 | chr2:66691362-66735606 | Ly4 |
|
| | 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 |
| GH02I066494 | chr2 | 66721174 | 66724343 |
|
Enhancer Sequence | CATAGACCAC CTGGATCTGA ATGGCTGCGA TCTGGGGCCC TTTCCCAGTT TTGCATGGCA 60
GATGAGGAAA ATGCAGGAAA CGCTGAGGCT TTGAAGATGT GCTAGAACCT CAGCAACACA 120
GAGCCACTGA GCAGCAAGAG GAGGCTGAGA CAGGGCAGAA ACACCCCCAC TGTTAAGAGT 180
GATGAGGGTT TGGAGCACCT AATCTGGATC TAGAAATTGG CCGCTGTGCA GGCAGCTGGG 240
TGGTTCAAGA TCTAGCACCC AAAGAGTGTA GCAAGTTCAG GCCTGGGCAT TTCGGCATAA 300
CCAGTCTGGT AGGTGGGGCC AGCAAGAAGG AATTCTAGGC CACAGGCCAA TTCAGAAGTC 360
AGGCAGGCCT ACGATTGGTA TTCGGAGATC TGTTTGGGAA GAGATGATCA TCCCTCCAGC 420
TGGCAGCACA GGAGAGCAGT ATTCAGTTCT GGGGAAAGAA AGGGCTGGGC CAGGGGAGGG 480
GAAGAGAGAT TCCCAGCCAG CTGATGTTGG AGAGAAGACT AGATCCAGAA GAGGACCAAG 540
AGCAGAGAAG GAAGTAATTC CTTGGTTTCT GTGACTTCTT TCTCACCCAA GATAGATTTC 600
AGGTTAGCAC ACTGTGACGT CATCACTGAA AACCTCTCCC CTCCCCTCGG GCGTGGGGGG 660
CAGTGTGTGA CTGTTCTTTA CTCCAGGCTG GTGATTCAGG AGGCAGCCTT GTTTGTGTTT 720
CCGTATGCCT CCTGCAGGGG AGACTTGCTT TTCTTTGATA CATAAATGGT GAGTGAAAAG 780
TAACTCTCCT GTGAGCTTGG TCTCTTTTTT GCTCTTCTCT GGTCGAGCAG CCTGACCAGG 840
CCTGGTCAGT GTGAATTGCC CAATTTCATA GTGTGCACGG GGGTCTCAGG AGAGGGCAAT 900
TGCCTCATAA CTTTTCTATT AGCAGAATTT CAGATTCCTG ACGTGGAGCG ATACTTGAAA 960
ACCATTTGCG TGATGCTGGG AAATGTTTGC TTTGTCCTTC TTTATGTCCT AGGCATGGGC 1020
ATTTTTGTCA TTTCACTGGG GACTACTTGT AGGCTCTGAA AGCAGGAAGG GGCTTCTCTC 1080
AGGCCATGCC CTAGCTAAGC GAGGATTCCC CTCTGTATTT GGATAGCTGG TTGCTCAAGT 1140
TCCAACCCTT ACATGAGGTT TTTCTGTATG ATTTTCTCCT TTATGTTTTG GAGGCACACT 1200
CGGGAACGTT CTCGTTTTTT TTTGTTTGTT TTGCAATGTG GCTATTTTTG ACTTTACAAA 1260
GCATTGGAAC TGGCATCCTC CCATTCTTGT GAACTTTCTC TGGATCTGTA 1310
|
