| Tag | Content |
|---|
EnhancerAtlas ID | HS003-19437 |
Organism | Homo sapiens |
Tissue/cell | A549 |
Coordinate | chr17:34985460-34986590 |
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 | GCAGGCTTCA TGCACACGGT GGGGCCTCTT CTGGGTCTGA CAATGCCTTA GCCCCTGTTC 60
TTTGAGGCTC TTGTTTAAGA TTTGCCAAAA AGAGGTCACC CAAATTATGG CCGATTTAGA 120
AAGTTTACTT TTCACCAGTG CACACAAAAT AGTGCAAAGA GATTAGGCTC TTCGAAAGGT 180
CATTTTAAGC CTTTCAAATA GTGACAGGGC CCTCCAGGCA GTGTCATCCT ACATTCTCAC 240
ACTGCAAGGG GACTGCCCTC GCTGGATTCT AGGGTCTCTC CCATGACTGG AGGAAAAGTG 300
TCATCTGGAC ACTATGTCAG AAGTCTAGAT TTGGCGCCCT CTGTGAGTCT GAGGGCGTCT 360
CCCCTTCTGC ACCCGGCCAC CCCCATGAGA GGTCCTGCCA AGTGGGTGAG CTGCGGCGGC 420
AGGCAGGGGT GCAGTGCCCA TCATTCACAC TAGATGGCGC TCTGACATTG GACAATCCTC 480
TGAGCATGTG GCTGCCTAGT GGCCAGAGGG CAGGGCTGGA TGGCTTTGAG GGGAGGCTGG 540
TCTCACTGGA CCTGACACCC CGACCTAGGG TAGGCCAAGG GGCGCCGGAG ATGTCAGAAG 600
CCAGGCTGGG GACCAGGAAC TCTGCTCCTC CACCCGTGAC TCCTGGTCAT TCTTGGGTCG 660
GGGCTGAAAG CGGGGCAGTG GGAGGAGCAG AGGGACCAGA GGGCAGCTGG AGGGGAGGGA 720
TGGGGTGGGG GGGGGCACAT CAGCAGGCCC TGGTGGGGCA GCCCGGCACC CCTCAGCCAG 780
TTAAGGGCCT GGGGAAGGTT GTCCTCTCAT TGACCACTAA AGCCTAGGGC TGTAGACCTG 840
GGGTCTCCCA GGAGTGGTTT GGCCATCTGC CTTGCCCTTG GACAAGGGGG CTGGGTAAGA 900
GGCATGGGGG CTTGTTTACA ATGCCTGCAG CTGGTAGGAA AGGAAGCCTT GGCAGATGTG 960
ACTGAAGGAT CAGCTTTGCT TGGAGAGCAA GACCCAGGCA CAGGACCTAA AGGCCTCAGG 1020
TTTGTGTCCC TGTTTAGGCA TGTGACCTTG GGCAAGCCAC TAAGACCTCT GCTTCCTAAT 1080
CGTTTCTGCT TTCAGAGTTG GGAACCTTGA ATGAGATCAT GCACACAAAG 1130
|
