| Tag | Content |
|---|
EnhancerAtlas ID | HS047-19116 |
Organism | Homo sapiens |
Tissue/cell | Fetal_placenta |
Coordinate | chr2:66722580-66723970 |
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 | TGCCCCAAAT ATAACAGAGA TGCCTGACTT ATGGAGAGTT ACTTCAGAGA TGTTTCTGGA 60
AGAAAGAGTT CTTTGGGTAT AAATGAGAAA CAAGGGGACA GTTGTGTTTC CCACACCATA 120
TTTTGGTATC TAGCATGTAA ATTATACTCT CATAGACCAC CTGGATCTGA ATGGCTGCGA 180
TCTGGGGCCC TTTCCCAGTT TTGCATGGCA GATGAGGAAA ATGCAGGAAA CGCTGAGGCT 240
TTGAAGATGT GCTAGAACCT CAGCAACACA GAGCCACTGA GCAGCAAGAG GAGGCTGAGA 300
CAGGGCAGAA ACACCCCCAC TGTTAAGAGT GATGAGGGTT TGGAGCACCT AATCTGGATC 360
TAGAAATTGG CCGCTGTGCA GGCAGCTGGG TGGTTCAAGA TCTAGCACCC AAAGAGTGTA 420
GCAAGTTCAG GCCTGGGCAT TTCGGCATAA CCAGTCTGGT AGGTGGGGCC AGCAAGAAGG 480
AATTCTAGGC CACAGGCCAA TTCAGAAGTC AGGCAGGCCT ACGATTGGTA TTCGGAGATC 540
TGTTTGGGAA GAGATGATCA TCCCTCCAGC TGGCAGCACA GGAGAGCAGT ATTCAGTTCT 600
GGGGAAAGAA AGGGCTGGGC CAGGGGAGGG GAAGAGAGAT TCCCAGCCAG CTGATGTTGG 660
AGAGAAGACT AGATCCAGAA GAGGACCAAG AGCAGAGAAG GAAGTAATTC CTTGGTTTCT 720
GTGACTTCTT TCTCACCCAA GATAGATTTC AGGTTAGCAC ACTGTGACGT CATCACTGAA 780
AACCTCTCCC CTCCCCTCGG GCGTGGGGGG CAGTGTGTGA CTGTTCTTTA CTCCAGGCTG 840
GTGATTCAGG AGGCAGCCTT GTTTGTGTTT CCGTATGCCT CCTGCAGGGG AGACTTGCTT 900
TTCTTTGATA CATAAATGGT GAGTGAAAAG TAACTCTCCT GTGAGCTTGG TCTCTTTTTT 960
GCTCTTCTCT GGTCGAGCAG CCTGACCAGG CCTGGTCAGT GTGAATTGCC CAATTTCATA 1020
GTGTGCACGG GGGTCTCAGG AGAGGGCAAT TGCCTCATAA CTTTTCTATT AGCAGAATTT 1080
CAGATTCCTG ACGTGGAGCG ATACTTGAAA ACCATTTGCG TGATGCTGGG AAATGTTTGC 1140
TTTGTCCTTC TTTATGTCCT AGGCATGGGC ATTTTTGTCA TTTCACTGGG GACTACTTGT 1200
AGGCTCTGAA AGCAGGAAGG GGCTTCTCTC AGGCCATGCC CTAGCTAAGC GAGGATTCCC 1260
CTCTGTATTT GGATAGCTGG TTGCTCAAGT TCCAACCCTT ACATGAGGTT TTTCTGTATG 1320
ATTTTCTCCT TTATGTTTTG GAGGCACACT CGGGAACGTT CTCGTTTTTT TTTGTTTGTT 1380
TTGCAATGTG 1390
|
