Tag | Content |
---|
EnhancerAtlas ID | HS091-06948 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr11:6459740-6461390 |
Target genes | Number: 12 | Name | Ensembl ID |
|
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
CTCF | MA0139.1 | chr11:6460393-6460412 | TTACCAGCAGAGGGAGCAG | + | 6.18 |
|
| 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 |
GH11I006439 | chr11 | 6460301 | 6460490 |
|
Enhancer Sequence | TGCATTCAAA AGTACTCTCT TTTTGACTGT GCATCCCCAG ATACTGCCAC TCTGCATTTA 60 CACACATTTT TTATCTACTG TGCTTATACG ATATCCTCCT GTGGCCCTAC ACATTCTCAG 120 TCCATCTGTG GACAACAATG TGCTGTCCTT TTGCACATTA CACACTCTCA GTTTGTGCAA 180 ATCCAGTCAC TATTACTATA ACACACATGC CTCTAGCTCT GTACCCAGAC ACTCCTGTGG 240 CACATTTATC TGCAACACTA TCAGTGTTGA CAAACATATC CACAACTGTT CATCCTGCAA 300 TCACCCATAC GTTATTTCTT CATTCATTTC TTCATTTATT TATTCATTCA TTCATTCATC 360 CAAGAAACAG TCACTGAATA ACTACTATAT GCCAGGCATT GTGAGAGGCA CTGAGGATAA 420 CAAGACTCTG TCTTTCACTT CAGGAAGTTC ACTGTACAAA AGCAGAAAGG ACTCCTGCAA 480 TCCTAGCCAT GCAACTACCA AGGTGTAGTG TAAAGAGTGC ACTGAGAATA TAGACAGAGT 540 GCCTAAGTCT GCCTAGAGAA GTTGTGGAAG GTTTCACACC AAAGAGGAAG CATTGGGCCC 600 AAGAGCTGAA AAATCAGCAG GAATTTTCCA GGTTGACAAG TGAGGAAAGG GTGTTACCAG 660 CAGAGGGAGC AGCATGCAGA GCCCAAACAT GAGGAAGCAG TGTGCTCCAA CCTCATGTAG 720 ATTCGTATGG CTGGCACACA GTGAATGTGG CAGGGGAGGA GATAAACCTG AGAAGATAAC 780 CAAGGCCCAG ATCATGAGAC CCTGTGTGCA CTTGGTTTGT AGTAATCAGG CACATTTTGG 840 GGTCATTTAC TGAAACAGGA AACACAGGAG GAAAGGTTGG TTTGTAAAGA AGATGCAAAG 900 CTTAGTTTGG GGGATGCTGA ATTTTAGGTG CCTGTAGAAC ATACAATTGG AAAGAGATGT 960 CTGGAGCTCA GAAAGTAGAT CTAGATCCAG TGTCCACAGC ATAGATATTC CTCAGAGCCA 1020 AGGTGATGGT TGAGATCACT GAGGGAAGGT ATATGGAAAG GCTAGGATGG ATCCCCAAGG 1080 AACATTAGGG AACTGGTTGA GATAGAATGA GACATTTGAG AAGAGAGAGA AAAGAGGCAG 1140 GAGGGAAAAC AAAGCCGACA GTCAGGACTT CCCCAACCAC ACAGCACCTT TGGCAAGGTA 1200 GGAAAAGGCA CCCCTTCCTC TGAGCAGACA CAGCCTGGGT CACATGGGAC TTGGTGAGCA 1260 CAGCAGACTG GATTTCATGC TCCACATGCT CTTCTAGCCA GGTGCCATTG TGTTGGGAAC 1320 AACTTGCCTT GCCCTATGAA GAGGACTTGA TACAGGGTCA TGGAAGGCAA GGGAAGCAAT 1380 TGCCAGAGAA AAAAAGGATG GCCAGCAGTG TGAGGTACAG CAGAGCGGTG TAGAACTAAG 1440 ACTAGGACTG AAGAACAGCC ACTGGATGGT GCACCTGCCA GGCCCACACG CATGCACACT 1500 CCCTTAGCCC AAGCTTTTAC AGGAAAGGAG GGCACATGGG AAAGAAATCT GCTACCTATT 1560 GCTATGGGCT CCATGCCAAG GCCATTTGGG GGAAGGGTCC CCAGTGTCGA TTCCAGCCCT 1620 TTCCAGCCTG GCCCTGATTT TGGCCCAGCA 1650
|