Tag | Content |
---|
EnhancerAtlas ID | HS091-09307 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr12:7274450-7276270 |
Target genes | Number: 32 | Name | Ensembl ID |
|
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
NFAT5 | MA0606.1 | chr12:7275432-7275442 | ATTTTCCATT | + | 6.02 | NFATC1 | MA0624.1 | chr12:7275432-7275442 | ATTTTCCATT | + | 6.02 | NFATC3 | MA0625.1 | chr12:7275432-7275442 | ATTTTCCATT | + | 6.02 | Nr5a2 | MA0505.1 | chr12:7275760-7275775 | GCTGGCCTTGACCCT | - | 6.55 | RREB1 | MA0073.1 | chr12:7274698-7274718 | TGTGTGTGTGTGTGTGGTGG | - | 6.41 | ZNF263 | MA0528.1 | chr12:7274733-7274754 | GAAGGTGGTGGAGGAGGGAGG | + | 6.3 |
|
| 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 |
GH12I007121 | chr12 | 7274481 | 7278367 |
|
Enhancer Sequence | CTGGAGTTTA AGACTCTGGC CAACCAAGTC AACTCCACAA CTTTGTGTGT CCCTGGGAGG 60 GTCTGGTGTG GGACCCACCT GTCTGTGGCC CTCGTCCCCT CCCCTGCCCT TTCTCCACTC 120 ACATCTTGGT CCCTCTGGTG ATTATCTCTT CCCTCTGAGG ACAGATGGAA CCTGATTTGA 180 ATGAGGGGTA ATGGTCTTGT GAGGACCAGG ACATGGATTG GGTGTGTGTT TATATGTGTG 240 TGTGTGTATG TGTGTGTGTG TGTGGTGGGA ATGGAATATC AGAGAAGGTG GTGGAGGAGG 300 GAGGATTGAA TTTGGAGAAT CCCTGGCTTC TAGTGTCCGC AGGGGAAACA GCAGCTCCAG 360 CTTCCCACAG CGGTCCCCTC CCCTCTGCAG GTCGAGCTCC CACCCTCTTG GAAATGCCTC 420 TGAAGCTGCA TAGTCCTCCC CTGATGCTTG TGCTCCCTTA GGGGATCTCC AGGCCTTTGG 480 GTGTGGTCTG GCCCCTGGAG AAGTGTGGTC GAGTGGAGGA TGGGGTCCTG CAGTGGCCAT 540 GTTCTGGACG CCCACATCAC GGGGAGTTTT GAGGGATTGA GCCCACTTTA GCTTGGGTCT 600 TAAAACCACC ATGGTAAGAA GTGTCAACCT TTGGGGGAAA AATAAAAATA TATAGAAATA 660 TTTAGAAAAA CCCACCATGG GGGCCTACAA GTTCCTGAGT CAAGGCCTCT GCCGAGACTC 720 CACTGACCAG CATGGTCACT GAAGGGCATG GAGGACCGTC CTGTGGGAAG AGGCTTGGAC 780 ATGCACTGTG AACTCAAGAG CAAGGACACT GTGTTGATCT GGAGATGTGG GCAATGGGCG 840 AGTACACACG GAGCATCCTC CTGTGCCTTG GAATGGGACA AGGTGGATTC CAGCAGCCCT 900 CAGAGCTTCT GCTGGGTGGC TTTGCAAAGA AGGGGCTTTC CACTCTACTG TGGACATCTG 960 CAGAGATTGG GCAGGGAATA AGATTTTCCA TTCAACCCTG AGTTCCTTTT TTTTTTCTAT 1020 TCCAAATTCA TTCCAGAGCA TGTGGTAGGA TCAGTATCAC AAGCCCCTAG TTCTTGGCCA 1080 GAGCCCTAGT GACTGTCTTG TGTGCATGGG GGGGCCAGCC GTTGCAGGAA GATGGGTCAA 1140 GAGTCTTCAT CTGATGAGGG CCAGGGACTT TCCAACTCCC TCAACCCTTC CCCCAGGCTC 1200 TTTTCCCACC CTCACATTGA GCCCTCTTCA CTCTGATAGT TGGGCCCCCT AGGACTTTTA 1260 TTCTGAAAGA GCCAAGGCCC CTGGAGGTGG AGAGGAGGCC AGAGGCTGGA GCTGGCCTTG 1320 ACCCTGAGCC AGCTCCACCC TTCTGGGCTG TTTTCCAAGG CAGCAACTCT GGGACCCTTG 1380 CTGTCCTCAG CTCTCCTCTT TATCTCTGGT CTCCAGCCTT GCTGGCCTTT GAGCAGAGGG 1440 TCCCTATAGC CAGGACTGCT GGGCTTCTCC CTCCTATGCC TTCACACCCC TGTATTACTG 1500 TCTTTTATTC CTTGACCTCA CATCCTCCGT CTACTTCCTT TTTCAGCTTT TTCTGGCTTT 1560 CTTGCTGCTT GCCCTTCCCA AAGCAGACAC GGAGGACAGG TCACCATTTA GAAGCTCCCC 1620 GCCTCCCCAA GCACTGGACA AAGGTCTTAC CCCATTCCAT CCCTCATTCC CAACACATAG 1680 GATGGAAGTA TCAAATGGCC AGATGCCTTC AGATGTCAGA ACCGTGGAGT CCGTTGAACC 1740 CTGTGTGTGG GGGGCTGTGT CTTGGGCCTG GTTTTGTTGA GCACATGAGA CTTTCTCAAG 1800 GATAAGGACA AAGAAATGGA 1820
|