| Tag | Content |
|---|
EnhancerAtlas ID | HS184-13214 |
Organism | Homo sapiens |
Tissue/cell | T47D |
Coordinate | chr17:26819260-26820580 |
Target genes | | Number: 23 | Name | Ensembl ID |
|
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| HSF1 | MA0486.2 | chr17:26819400-26819413 | GAAGATTCCAGAA | - | 6.2 | | HSF1 | MA0486.2 | chr17:26819624-26819637 | GAAGGTTCTGGAA | - | 6.3 | | PLAG1 | MA0163.1 | chr17:26820367-26820381 | GGGGCTCAATGGGG | + | 6.22 | | RARA(var.2) | MA0730.1 | chr17:26820476-26820493 | TGACCCTGAGATGCCCT | - | 6.08 |
|
| | 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 |
| GH17I028493 | chr17 | 26820109 | 26821001 |
|
Enhancer Sequence | AGAATACTAG AAGGCACTGG GCACAGTCCC TGTCCTTGTA GCCCATCAGG TGGATGATGA 60
TATGGTGGGG TCACGACAGA GGGAAGCCCA GATGCTGCAA GAGCACAGAG AACACAGTGT 120
CTAGTTCAGC CCAGGTGAGT GAAGATTCCA GAACACCATG GAGGAGATCA TGCCTGGGCT 180
GAATCTTGCA GGACTAGAAG TCAGCCAGGT AGAGAATGGG TGAAGAAATT CCAGGCAGCA 240
GGAGCAGATT GCACAAAGCA CAGAGGCAAG ACAAGACGTG TTCGAGGGAA CTCTAGTTCT 300
GCAGGACTAA AACACAAACA GCAAAAAGGA GCATCAGGTC ATGAAGCTGG AGAAGTAGGC 360
AGGGGAAGGT TCTGGAAGCT CTTGTGTGCC ACCTAATGAA GCCAAGAGTA ATAAATAGAT 420
TTCATTCCTA CTTCCACCAG GTTCCTGGTA GTCACTGTTT GGAGCTCTGA GTTGGAAAAT 480
CATAGGAGAC CCTGCTAAGG CTCAGTTAGT ATCAAGTCTG TGATTGATTA GTGATGTCTG 540
CCATGAATAC GGGATAAGAG TGGTGGTATG AGTGTTACTG TGGTATTAAT TATAATTTGC 600
CCTTCCTGCC CAGGCAGTGG AGAGCCCTTG AAAGTTTTTA AGCATTGCTG CTGCACTTTG 660
GAAAAATCAC TTGGGCAAAT GTAAGGAAGC TGGATTAAGG TTGGGAGCTG GTACAAGGCA 720
AGGTGGTAGT AGAAGAGGTC AGCACAGTGC CAGGCACCAC AGGGGAGTCA AAGATGTGTG 780
AAGTGTGGTC TTTGCCCTTG AGGAACTCAC AGTCCAGCAG GGAGGTTGAG ATTTACCCAA 840
GTGGAAAGTT AAATGTCAAC ACAAGTTAAG TCAGCAGCAG AAGGAAGTGG GCTGCAGCCT 900
ACTGTGCCTC TGAGGACAAT GCAGGTGGGG CTCAGGCTGG CAGGGGATAA GCAGAGAAGG 960
CAGAGGAGGG AAGGGAGGAC TTCCCGAAGG CTGTTGGAGG AGAAGAGCTG TGAGCCAGGG 1020
CAGGAAGAAG TCCCAGGGTC TGAGCTGCTA GGTCCTCCTC ACCCTGGGCA AGGGAGGGTT 1080
CAGCACCATA GAACCCCTGG AGGAAAAGGG GCTCAATGGG GCAGGGCCAA GCATGGAGAA 1140
TAAGCAAGAA CTATGGCCTC TAAAAGTCTT CTGCTCCTCC TCCAGAACCT CAGGCGGAGC 1200
TGGGGCCTGA GTGTAGTGAC CCTGAGATGC CCTCTGTGGG CCTCAGCCTT TAGATGGTAG 1260
GCACTCAGAG CCCCTTGCTC CCTGCTGGAG CAGGCCCCCC ACGAGCTGCC CCGTCCCTCT 1320
|
