Tag | Content |
---|
EnhancerAtlas ID | HS091-17367 | Organism | Homo sapiens | Tissue/cell | HepG2 | Coordinate | chr16:53556520-53559020 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Mafb | MA0117.2 | chr16:53556544-53556556 | AGTCAGCAATTT | - | 6.92 | ZNF263 | MA0528.1 | chr16:53557364-53557385 | TCCTCCCCACTCCCTTCCCTC | - | 6.03 | Zfx | MA0146.2 | chr16:53556805-53556819 | CCCGCCTCGGCCTC | + | 6.01 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr16 | 53557634 | 53557753 | chr16 | 53558138 | 53558316 |
| Enhancer Sequence | TATTTTGGTT TAGTTATATA AATAAGTCAG CAATTTTTTT TTTTTTTTTT TTTTTTTGAG 60 ACAGGGTCTC ACTCTGTCAC CCAGGCTGGA GTGCAGTGGC GTGATCTCTC AGCTCACTGC 120 AACCTCTGCC TCCCGGGTTC AAGCGATCCT TCCACCTCAG CCTCCCGAGT AGCTGGAATT 180 ATGGGTGCAA GCCACCATGC CTGGCAAATT TTTCTATTTC TTATAGAGAC AGGGTTTTGT 240 CATGTTGCCC AGGCTGGTCT CGAACTTCTG GGCTCAAGCA ATCCTCCCGC CTCGGCCTCC 300 CAAAGTGTTG GGATCACAGG CATGAGCCAC CGCGCCCAGC CCCTGGCAAA ACTTTTTTAC 360 CCACTTTCTT CCCTATGGAA GATAAACTCG AGAGGAACAA CTTCTAACTG ACCTGCTGCT 420 CTCCTCACTG ACCTGCTGCT GGTGTCTCCA ACTGTCGCTG CCTTCTTAAT GCTGGCAAGC 480 TCAGGGCTCA GCCTGAGACC TCACCTATGG TCACCTGCTT GGTGACACAC CCTGGGCTCC 540 AGCCTCTCTC CTGATCTTCT GACTCCTGAA CTCCAGGCTC CTGTAACCAG CTGCTCCTTC 600 CTCATCTTCA CTCGAATTTG ATCATCTCAA AGCCAACACA TCTCCGTGCC ACAGCGTACC 660 TCATCCCTGA GGGCCTCCCG TTTTGTAAAT GGCAATGCTA CGCTTCCAGC TGTTCGGGTC 720 CATAACCCTA CGGTCATCCT CTCATCTCAT GCCCCACGCG TCACTCGTCA GCAGATGCAG 780 GAGCCCCATT TTCGTCTGTA TCCAGAATCC AGTCATTTCT TGCTGCCTTG CCTGCGGCCA 840 TCCCTCCTCC CCACTCCCTT CCCTCACCTG GGTGACTGTT AGAGCCTGTG GATTGACTTC 900 TCCACATTCT TCCCACAAGC CCGGCCACCG TGATCCGGTT AAAGCCTAAC TCAGGCCACT 960 CTTCTGTTAA GCTCCCAGAG CTTTCCCATC TCAGAGTAAA GTCCAGAGTG CTTGTGCCAT 1020 ACCATCAGGC CCTGTCCGAG TTTCCTCCTC CCTTGCCCTA GTCTCCTGCC ACTCTCCTCC 1080 CGGGCTCCTG CAGTGGCGGC CACAGTCCCA GTACCCTCTG GCTCTGCCTC CGGTGCACCG 1140 AGCACAGGGC ATTTGCACTT GCCGTTTCCC TCTGCCTGAA ATTCTTCCAG ACAACTACAT 1200 CACTTGCCTC CCCACTTCCT TCAGGCCTTT ACTCAAACAG CACCTTCTCT GAGAGGTGTT 1260 CCTCGCCCCT CTATCTACAG CGGCAAGCCT CCCGCCCTCG GCCTCCTTCT CTCTGCCTAC 1320 CTCATGCCAA CACTCCCTCT CCCGCTGGTT CCCTAGCCCT TCTTGCCATG CAGCAAACAG 1380 TGTGCTTTAC TTATTGTGTA TATTATCTGG AAAGGGCACT CCACGAGGGC AGGAATGCTC 1440 ACAGCTGTCC TAGCATCTGG AGCAATGCAC CTAGCGGGTG CTGAATGAAT ATCTGTGGAA 1500 TGAGTGAGTC CTCTGCTCGG CTCCTGGTCG GTGGCTGCTG GCCTGCCTGT GTCCGTGCTC 1560 CACAGTGGAC CGGCCCCTCC TCGGGGGCTT CTCTGACAGG CGCACACTGC AGGCCTGGGA 1620 ATCACACCTG GCATGGGCTA CCGCCCTGAC TGCACTCCCC AGGCAGAGTC CTAATGTCTG 1680 CTCTGCCTTT GGAGCTGCTC TGAAGTTACC CTGGAGCACG GACCAGATGT CCAGATACCC 1740 ACGGAGGCCA GACAGGGCAC AGAAATGAGG GACTCGGGCC AGGCCAGGGA AGGTACAGGC 1800 CCAGCCCGAG GGACGGCCAC TGCTCAGCTC TGGTCAGTGG GTACCAGGCA TGGATGTGTT 1860 TTACAGTCAT TAAAAGTCTT TGGTTTTTCC AGGGAAAGTG GAAATCTGGA TTTTTTAAAA 1920 AATGGCATGG CTGGGCGCCA TGGCTCATGC CTGTAATCCC AATGCTTCCG GAGGCTAAGA 1980 CGAGAGAACT GCTTGAGCCA GGAGTCTGAG GCTAGCCTGG GCGGTATACT GAGACCCTGT 2040 CTCTACATAT CATTTTTTAA AAGTTAGTTG CATGTGGCGG CGCATGCCAG TGGTACCAGC 2100 TACTCAGGAG GCTGAGGTGG GAGGAATACT TGAGCCCAGG CAGTTGAGAC TGCAGTGAGC 2160 TGTGATTGTG CCACTGCACT CTAGCCTGGG TGACAGAGCT AGACTCCATC TTATAAATAA 2220 ATAGATAAAT AAGCCAGGCA TGGTGGCTGA CACCTATAAT CCCAGCACTT TGGGAGGCTG 2280 AGGCAGGCAG ATCACTTGAG GTCAGGAGTT TGAGACCAGC CTAGCCAACG CAGCAAAACC 2340 CCATCTCTAC TGAAAATGCA AAAATTAGCT GGGTGTGGTG GTACATGCCT GTAATCCCAG 2400 CTACTAAAGA GACTAAAGCA TGAGAATCAC TTGAACCCGG GAGGCGGAGG TTGCAGTGAA 2460 CTGAGATCGT GCCACTGCAT TTCAGCCTGG CGGACACAGT 2500
|
| |
|
|
|