| Tag | Content |
|---|
EnhancerAtlas ID | HS108-16694 |
Organism | Homo sapiens |
Tissue/cell | K562 |
Coordinate | chr17:34985580-34986480 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| RREB1 | MA0073.1 | chr17:34986175-34986195 | AGGGATGGGGTGGGGGGGGG | - | 6.22 | | ZNF263 | MA0528.1 | chr17:34986174-34986195 | GAGGGATGGGGTGGGGGGGGG | + | 6.38 |
|
| | 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 |
| GH17I036629 | chr17 | 34985821 | 34986010 |
|
Enhancer Sequence | AAGTTTACTT TTCACCAGTG CACACAAAAT AGTGCAAAGA GATTAGGCTC TTCGAAAGGT 60
CATTTTAAGC CTTTCAAATA GTGACAGGGC CCTCCAGGCA GTGTCATCCT ACATTCTCAC 120
ACTGCAAGGG GACTGCCCTC GCTGGATTCT AGGGTCTCTC CCATGACTGG AGGAAAAGTG 180
TCATCTGGAC ACTATGTCAG AAGTCTAGAT TTGGCGCCCT CTGTGAGTCT GAGGGCGTCT 240
CCCCTTCTGC ACCCGGCCAC CCCCATGAGA GGTCCTGCCA AGTGGGTGAG CTGCGGCGGC 300
AGGCAGGGGT GCAGTGCCCA TCATTCACAC TAGATGGCGC TCTGACATTG GACAATCCTC 360
TGAGCATGTG GCTGCCTAGT GGCCAGAGGG CAGGGCTGGA TGGCTTTGAG GGGAGGCTGG 420
TCTCACTGGA CCTGACACCC CGACCTAGGG TAGGCCAAGG GGCGCCGGAG ATGTCAGAAG 480
CCAGGCTGGG GACCAGGAAC TCTGCTCCTC CACCCGTGAC TCCTGGTCAT TCTTGGGTCG 540
GGGCTGAAAG CGGGGCAGTG GGAGGAGCAG AGGGACCAGA GGGCAGCTGG AGGGGAGGGA 600
TGGGGTGGGG GGGGGCACAT CAGCAGGCCC TGGTGGGGCA GCCCGGCACC CCTCAGCCAG 660
TTAAGGGCCT GGGGAAGGTT GTCCTCTCAT TGACCACTAA AGCCTAGGGC TGTAGACCTG 720
GGGTCTCCCA GGAGTGGTTT GGCCATCTGC CTTGCCCTTG GACAAGGGGG CTGGGTAAGA 780
GGCATGGGGG CTTGTTTACA ATGCCTGCAG CTGGTAGGAA AGGAAGCCTT GGCAGATGTG 840
ACTGAAGGAT CAGCTTTGCT TGGAGAGCAA GACCCAGGCA CAGGACCTAA AGGCCTCAGG 900
|
