| Tag | Content |
|---|
EnhancerAtlas ID | HS108-18103 |
Organism | Homo sapiens |
Tissue/cell | K562 |
Coordinate | chr17:80111370-80112630 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| BHLHE40 | MA0464.2 | chr17:80111414-80111424 | GTCACGTGAT | - | 6.02 | | Myog | MA0500.1 | chr17:80111628-80111639 | CAGCAGCTGTC | - | 6.14 | | TFEB | MA0692.1 | chr17:80111414-80111424 | GTCACGTGAT | - | 6.02 | | Tcf12 | MA0521.1 | chr17:80111628-80111639 | CAGCAGCTGTC | - | 6.02 |
|
| | 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 |
| GH17I082151 | chr17 | 80109495 | 80112030 |
|
Enhancer Sequence | ACAGGCAAAG GAAGGAGGGC ATGGATCACA GGGCCCATGT CCTAGTCACG TGATTCTGCA 60
CACAGTGACC TGGGGGGCAG GGAGTGAACG ATTCTACTTC TCTCGGATTC AGTTTCTGGT 120
AAAATGTTAT TTGGTAAAAG TTTATTTTGA TGATTCTCTA AAATCTTTCC ACAAAATAAG 180
ATTTCTACAG CCTGAGACAT ATTCAGGAAT GTCTTCACCA CTGTGTGCTC CAAGGGCTGC 240
CCACCCCCAG CAGGGCAGCA GCAGCTGTCC ACCCATCTGC CCCCACGCCT AGGACTGCCC 300
CAGCACCCCA CAGGTGAGGA GGAGATGTCT CCAAGTATCT GGACGATTCG AAGAAAATTC 360
GAAGGAAACT TTGGTCTGCT GAAATGTCTT CACGTCCTGA GGACATGTAT GAGTGAGTGA 420
CACAGGGAAG TCCTTCTCAG AGGCTGAGGC CTGGGCCTGG TACAGTGGGT TCCATCAGGC 480
TGGGCCGGCG CTCACCGCCC CACACAGCCA CTCCAACGCC TCTCGGCAGA GCCAGCACCA 540
ACACCATGGC CAACACTGCC CCCCAGTGGA CCCAGGGATG TAACACATCC CCCAACTCAG 600
CCCTGGCGGC CAGTGACTGG GGGAAGTTTT GTATTTTAAG GGCTAGAGGC AGCTGATGTG 660
GGTGGTGCAG TCAGGGAAGC CCAAAGCCAG GCTGTGCGGC TCAGCCCAGT GGGACCTGCC 720
TGGGAGCAGA GTGCCCCACT GTTGTCCACA GGCTCTCCCT CTGCCATGGG AGAAGTGGGA 780
ACACGTGCCT CCGCACACAC CTGGTCCCAG CTTTGCAGAC CTGGCTCCTT GGCTAGGGCC 840
GTGGAAGGGG ACCAGCTTTC GTCAGGAGTG CTGTGGGACA GTCCCTGGAC CCCTGTGCAC 900
TTCCTCACCC ACCCTGCACT GGCTTCCTGC ACTACAGGAG GTAGGCTGGA GACGCAGTGC 960
CGCGTCACAC CTCAGTACTT GGGTGGGTGT ACACAATACG TGACCTGGTC CGTGGCCCGT 1020
GTGCAAATGT CACCAACCGT CCAGATAACG CCCTGACGCC ATCTCTCCTG TGCAGGGTCC 1080
AGGGTCCCAC GTGGCATTTC TACACTGTCT CTCCTGTGCA GGGTCCATGG TCCCACATGG 1140
TGTTTCTACA GATGATGCCC TGACACCGTC TCTCCTGTGC AGGGTCCAGG GTCCCACGTG 1200
GTGTTTCTAC GGATGATGCC CTGACGCCGT CTCTCCTGTG CAGGGTCCAG GGTCCCACGT 1260
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