| Tag | Content |
|---|
EnhancerAtlas ID | HS091-24160 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr19:42538620-42540000 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chr19:42539055-42539074 | TGCTGCCCCCTAGTGGCCA | - | 9.21 | | E2F6 | MA0471.1 | chr19:42539013-42539024 | GGGCGGGAAGG | + | 6.62 |
|
| | 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 |
| GH19I042034 | chr19 | 42538481 | 42539552 |
|
Enhancer Sequence | CCCTCACTTT TTCCCCTCAA CCACACTTTT CCCCTCAAGT CTTTATACAT ATGGGCTCTC 60
TACTTGGAAA ACACTCTTCC CCAGATCCAT CCTTTCACTT GGCAATTATT TGCTGCGCAC 120
CAGCTGGGTG TCAGATGGTT CTAGGCGCTG GGGATGCAGA AGTAAGGAAA ATAGTCAAAC 180
TTCTGCCCTC ATAAAACCCT CCCTGGTGGC TCTTCTCAGG ACTGTATTCC CCACCCCTTT 240
TAGGTCTCTT CTCAAACGTT ATCCAACCAC CTTGTCTAAA ACAGCATCCA CGCACCAGAC 300
ACTTTTATCT CCTTACCTTG CTTCACCTAA CACGATATTA ATATATCATA CGCTGTCAGT 360
TTCCCCCACT AGAACATCAG CAGTTGGGGC GGGGGGCGGG AAGGAGGGGA CAAGGAGCAC 420
CTCTGCTCAT TACATTGCTG CCCCCTAGTG GCCAGGATGC AGTGGGTGCA GAATAGTTGC 480
TCAGTAGTTA TTCAGTAAGT GAATGACTAA ATGTAGCTGG TTTGTTTTTG TTTTCGTTTC 540
GCTCTTGTTG CCCAGGCTGG AGTGCAATGG CACCATCTCG GCTCACCACA ACCTCTGCCT 600
CCCAGGTTCA AGCAATTCTC CTGCCTCAGC CCCCTGAGTA GCTGGGATTA CAGGCATGCG 660
CCACCACATC CAGCTAATTT TTTTGTATTT TCAGTAGAGA TGGGGTTTCT CCATGTTGGT 720
CAGGCTGGTC TCGAATTCCC AACCTCAGGT GATCCGCCCA CCTCGGCCTC CCAAAGTGCT 780
GGGATTATAG GCGTGAGTCA CTGCGCCTGG CCTAAACGTA GCTGTTTTTA AAGATGAGGC 840
AGATCTATGT GTACTAACGT GGGAAGATGG CCAAGTTACA AGTAAAAAAA GCAAACTACA 900
CAGCAGTAAG TATAGTAAGA TATCATTTTT GCAAAAATAA AAATTTAAGA AATTTAGGCT 960
GGGCATGGTG GCTTACGCCT TTAATCCCAG CACCTTGGGA GGCCGAGGTG AGCAGATCAC 1020
CTGAGGTCAG GAGTCGAGAC CAGCCTGGCC TACATGGTGA AATCCCCATC TCTACTAAAC 1080
AATACAAAAA AATTAGCCTG GCATGGTGGT GGGCGCCTGT AATCCCAGCT ACTTGGGAGG 1140
CTGAGGCAGA AGAATTGCTT GAACCTGGGA GGTGGAGGTT GCAGTGAGCC AAGATCGTGC 1200
CACTGCACGC CAGCCTGGGG AACAGAGCCA GACTCTGTCT CAAAAAAATT AAGAAATTTA 1260
AAGATGTACC TGTATTAATG AATTTGTAGA AAATGAGTTG GAGGAATATG GTCTCTGAGG 1320
TGTAAGAACA TCATGTATAT CCAGTGTTTC TGCTATTTGT ACCATTTGGT ATTTTATCAT 1380
|
