| Tag | Content |
|---|
EnhancerAtlas ID | HS108-28153 |
Organism | Homo sapiens |
Tissue/cell | K562 |
Coordinate | chr3:52532100-52533010 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| RREB1 | MA0073.1 | chr3:52532274-52532294 | GGGGGGTGTGGGGTTGGGGG | - | 6.36 | | RREB1 | MA0073.1 | chr3:52532273-52532293 | CGGGGGGTGTGGGGTTGGGG | - | 6.3 |
|
| | 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 |
| GH03I052497 | chr3 | 52531761 | 52533425 |
|
Enhancer Sequence | CCTCTCTGAC AGGGTTTAGA TTCTGGGCTC TCAGCCTTAA AAAGTCCCCA TGAACCAGGT 60
CCCAGCTTGG GAGAATTTCA TCCACCTTCT CACCAAAGAC TTCACACTTC GTGTCTCCTC 120
AACTTCCCCC AGCAGCAGCT CTGTGGGAAG CAGACATTGC AAAATCAGGT CTGCGGGGGG 180
TGTGGGGTTG GGGGGGAGAC AGCACCCGCT CTGGCTCAGT CCCGAGGTGC CCCCAGGAAG 240
GAGGGAATCT GACTCAGCAC TCAGGCCGTG ATCCAGCCTC ACTCCACCCA GCTGGACCAA 300
CGGCAAGATG TGGGCTCAGA CCGCCGATGC TCCTTCCAGG CCATGGGGCG GAGGCAGGGC 360
CCCTCGGCTG TGGTCTCGGA GAAGCACTGA TGTGGCAGCA GGCTTACCAT TCATCAGCAT 420
TTCACACACG TTTACAAACA CCCAGGTCCT GTGAGTGAGT GTCCACACCA GGCCCCAAAG 480
CTCCCGCTTC CTTCTGGGCC CTAACTCACC CATCGCTCCA TCTAGCCCTG ACTGTCTCAG 540
AGTGCGACCA GCACAGTCTT ACTCAGCCTG AGCCCTTATC CAGAGCTGAC CACCATTCCT 600
CCAAGAGCTG GTCCACAGCC AGAATGGTGA CCGCGCTGGC AGCTTTGCCC AGCTGGCCAG 660
GTGGCTTTGA GGGGAGCCCA CCTCCTGCCA AGCCTCTACC CTGAGCCAGC AGCTGCTCAG 720
CCCTCAAGTT ACCCAATTTC CTAGTCTCTC CCTGGCTCAG CAAAGGCGAG CCTCAGGATG 780
GGGAACGAGA CCACAACATC CCAGCTCCGC CGTTCAACAC AGGCTGCTCT GAGCAACTTC 840
CCTGTTTGCA GACCGCAGAG GCATGAGCGG AAAAGGCCAA ATCACGGTAG CACAGAGGCT 900
CTGGGGCCCT 910
|
