| Tag | Content |
|---|
EnhancerAtlas ID | HS047-00225 |
Organism | Homo sapiens |
Tissue/cell | Fetal_placenta |
Coordinate | chr1:10555370-10556610 |
SNPs | | Number: 2 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| BCL6B | MA0731.1 | chr1:10555402-10555419 | CACTTTCTAGTAATTAA | + | 6.36 |
|
| | Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
| SE_20679 | chr1:10554552-10560342 | CD56 | | SE_36701 | chr1:10554348-10557363 | HMEC | | SE_47404 | chr1:10554801-10555893 | Panc1 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr1 | 10555407 | 10555592 | | chr1 | 10556180 | 10556393 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH01I010494 | chr1 | 10554671 | 10559336 |
|
Enhancer Sequence | AGCCGCTGGT AAGTACCCAA GATATGTGGT ATCACTTTCT AGTAATTAAA ATGCCACGCG 60
AGTGAAAAGA AACCTTCTGT TCCTATGGTT CTGCGTCAGT AGTGTCCCTT TAAAAGTAGC 120
TGTTACCTAG AGACTGCCTC TGTCAGTGAC CTCTGACTTC TCTTCTCGCG TGTGGGGACG 180
AGTGAGATCT CTCCTTAGTA AAGGCTGGTC CTTTCTAGGA CTAAAAGCAT CCACCCCAGA 240
TGGTCCTGCA CCACTTTGTT TGTGGCTGAT CAATAGTAAT TAGTGAGATT CCTGCGCCCG 300
TGGGAGGCTG AGGTGGAGTG AGGTGGCTGG GCTTCTAGAT TGTTTGAAGT AGCCGCCCTC 360
TGCTCTGCCC CTCAGGGTGC GAGCGCCTCA GTGGTCTTTA AAGAACAGGT AAGCGATGGA 420
ATTCTGGTTT TGCCTGGTCA GTAATTGTGT GATTGTCATT CCCAACGCTG TCTTCTTAGA 480
CTATGGATAG GGAAGAGGCC TATTAAGCAC TGCAGGTAAT TTTCTCTCCC AAGTGCTTTT 540
CATTTGGTGG CCAGAGTCCC AGGCTGCCCA CCCCATTTTC ATTCTTTTTT GCTTTTCAGG 600
GCCTGCTGTA AGTCCTCTTG GCTGGGTAGT AAGACTGGCT CTGTATAAAC CAGATAAGTT 660
TGATGGGAGA GCCAGCTCTA GGTTTAACTT TTCAGAGCTT TTTCTTCCTG CGTAGCGATA 720
GCAGGCGTAG GGCTGTACTG CCAAGGCTTT GTTTCAGCAG GGCCTGTGGT TTCACCTGTT 780
CTGCTTCACT CCCCTTCTGG CAGTCGCGGG AGGAGATGAC GTGAGGGACT TAGCGGGTAT 840
GAACACGTCT GAATTCCAGT GTGTACGAAG GCTTTCCCAG GCTGAGGGCG AGTTGGATCC 900
AGTTGAGCTG TCTGTAGAAA GGCCGAGGTG ATACAAGCAC TGCTGGGACT GTTTCAGGGG 960
AGCAGTGTTG TCATTCATGT CACCTGCTGT TACGTCACCA GTTACGGGCT TATATCCCAG 1020
CACTCCCACG GTGGCCTCGT TTCACTCTTT TGGTATTGCC CAGTTCCTTC CTTGAGGTCA 1080
TGGTGGTGGG AAAGCCCAGG AGGCCCCACC TTGCTAGTCT CTCCGGACGT CTGCCTGCTT 1140
CCCTGGGGCC TGCCTCAGTG CCCCTCAGGC CGAAGTTGTG GTTGTTTTAG ACTGAAGTGC 1200
AGATTGAACA CCATAGGCCG CTGCAGTCCT TTCCTTCCTC 1240
|
