Tag | Content |
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EnhancerAtlas ID | HS003-21204 |
Organism | Homo sapiens |
Tissue/cell | A549 |
Coordinate | chr17:78169450-78170440 |
Target genes | Number: 14 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
CTCF | MA0139.1 | chr17:78170059-78170078 | TGGCCACCAGGGGGCGCAA | + | 9.31 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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| Number: 2 | ID | Chromosome | Start | End |
GH17I080195 | chr17 | 78169699 | 78170170 | GH17I080196 | chr17 | 78170241 | 78170390 |
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Enhancer Sequence | GGTGAGCACG CCCAACCCTG AACCTCCACA GCAGTCCACC TCCCCTGGGC AGAGCAGGGA 60 GCTGATGAGA AAGCCGGGGC CTCTCTCCAG GGAAAGGGCA GATAGAAGCA GAGCTCAACT 120 TCTGCCCTGG GCCTTGACCT TGGCCTCGAC CTTGCACTTT GGGAAAGTCC CGCCTGCCAG 180 CCAGCGTAAG CCAAAGGCCG GCTGCGCTCT GTCTGCTGGT GTCCTTGTGT TTTTCCCTAG 240 AGCCAGGGGA GTTGTGTCTG ATCCACGCCC TGCTCAGCAC CCAGCCCCCT GCTCTGATCT 300 GTAACGCTTG GGCTTCCCAG TGGTTTCAGA AGGCAGCAGG CAGGGTGGCT TAGTGGTGCC 360 AGGCTGAGGC GAGGCACAGC GTGACATCTA CCTGCGGGGA GCATCTCTCC TCTCAGGCGC 420 TGGCCCTGAG GCCTCGCGCT TCTCCTGTAG CTCATTTCTG TTTGTGATTG GACCGGCCCT 480 CTCTGCTTCC CAAGTCCATG GGCCCGTCAT GGGTGGGTGC CTTAATCCTT TCCACCTCGG 540 CGCGACCGGC TCCCAGCCTT GGGCCTTGCA CACAGTAGGT GCTTTGCTCC CCATTTGGAA 600 TTCACCCCAT GGCCACCAGG GGGCGCAAGT GCCCTGCGCT GCCCCTGTGC CTTCTGTGGG 660 TCGCAGAATC AGAAATCTTC ATCTTTGGGG ACTCATACAC GTTTTTATTT ATAATCGTGA 720 TAAATCGAGA GAGACCACCC AAGGCATATC TAAATTAGAT GTGAGATGAG AAGAGGGGCT 780 TATTCCTCTT TATTTTTCCT CTGTGAGGAT TCTGCGTAAT GCCCTGGTTG CATATACTTT 840 TAGTGGAATT GACCTCAAAT ACATCCAGAG TACACAGCTC ATTTCATTGG CTTTGAATGT 900 GATCCCAATG GGTTTTTGCC TGTGAGCCAG GCCTAGGGAA CTCTCAGGTC TCTGCTGGCC 960 CTGGCTCTGC TGTGTGGTTC ACAGAGTGAG 990
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