| Tag | Content |
|---|
EnhancerAtlas ID | HS093-11959 | Organism | Homo sapiens | Tissue/cell | HL-60 | Coordinate | chr16:68743620-68744580 | SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
| TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| E2F6 | MA0471.1 | chr16:68744013-68744024 | GGGCGGGAAGG | + | 6.62 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | TACAGGCGTG AGCCACCGCG CCTGGCCTCC TTTTTCTGTC TCCTTCATTT CTAAAGACGG 60
CACCATCATC AGCCCAGCTG CCCAAACCAG AAACCTAAAC ACCTTGTCCT CAACTCCTTC 120
CTTTTATTGA CTGCCCATGC TGATCATCCA TGGAGTCCTC CCAGATATCC TGGAATTCAA 180
CCACTTCTGT CCATTCTCCA CCACCACCTT TGTCCCAGCC ACCAGCACCC CAACTGGGAT 240
GGCCACAATG GCCTCTGCGC TGGTTAATTC CCCGTTTCCC CCAGATCCAC TCTCTTCCCT 300
TCTTCCCGCT GCTCTGCAAC CAGGAGGCAG CCCTAGCTGC CCTGTGTTCT GGATTAGGTT 360
GGTTACATTG GGGGAAGGAA CCCACAGGAG ATGGGGCGGG AAGGAGGGGA AGTGGCAGTA 420
TCCCTCCGCC TGCTCCCTCC CTGCCGGGCT GGGTTTGGCA CTGGCTGCGC TCTGCACCCT 480
CTATGGCCAC AGCTCCTGTC ATGTGGACCC TCTTCCATGG CTCCAACACT CCCTGGGGTC 540
TGAAAGGCAG TTTCTGCACT TGCCCTGTTA GGACTAAGGG CTGCCCTGGC TTCCCATTTG 600
CTAGTCTGAG GATGCCTCGC CATCCCAGCT GGTCACCCTA ACCGAGTGGT TCTCAACCAG 660
GGGTAGTTAT GCCATCTCAG GGGATATTTG GCAATGTCTG GAGTCATTTG TGGTTGTTAC 720
CACTGGAGTG GGGGTGCTAC TGGCATCTAA TGAGTAGAGG CCAGAGATGT TGCTAAACCC 780
CCTACAATGC ACAGGACAGC CCCCACAGCA CATGATCCTC CCTCTGAAAA GTCAATAGAG 840
CTTAGATTGA AAAACTATGG CTGGGCGCGG TGGCTCACGC CTGTAATCCC AGCACTTTGG 900
AAGGCCGAGG CAGGCGGATC GCTTGAGACC AGCCTGGCCA ACATGGCAAA ACCCCGTCTC 960
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