Tag | Content |
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EnhancerAtlas ID | HS091-49443 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chrX:48398310-48399720 |
Target genes | Number: 25 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
REL | MA0101.1 | chrX:48398810-48398820 | GGAAATCCCC | - | 6.02 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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Enhancer Sequence | GAGGCTGGCG GTGAGTCGGC CCAGCCGCCG AGGCATCCCA GGGGAGGGGG AGGCGGTGGC 60 TGTCATAGGA TGGAGGGCGG GACCTGAGAT TTCGGACATA ACCTGAGCGG CGAAGCTTGA 120 GGGCCAAGTG ATGATGGCGA GGGGTAGGGA GGGCCTGAGA GCCTGAGAGC GTTAGCGACG 180 TACCTTGGGG CGTGGGACTG AAAATAGAGG GACGAGGCGG GGGTCTATGG GATGAATGGG 240 TGGAGCTTAT AGACAAAGGG GAGGGGCTAT GGGGCTGGAG GAGGGGCCGC AGTAGTTGAG 300 GGTGGGGCTC TGAGGAATGA GAAGGTGCTG GCTCTGGAGT CAGTCAACCC ATGTGTTGAG 360 AGTGCACTTA TGTGCAAGTT CCCACTTTGA TGAGCTGACA GGCTCGTGGG TGGAGACAAC 420 TAAAGAAATG AGATGCTTCG GACACTAAAA TAATGAAAAA GGTTATGAAA TAGGGAGTCA 480 CGTTAGCCAA GGTTGTACAG GGAAATCCCC AGAGGAGGTA TTGAAGGAGC AGAGACCCGA 540 ATAAAAGGAG TCAGCCATGT GCATATTAGA AGGGAAGAGT ATTCTAGGCA GAAGGAATAG 600 CAAGGGCAAA GACTAGAGGA TGGGAATGAG CCTGGCATGT TCCCGTAGGT TCCTGATTGC 660 TGGAGTGGAG AGAATGAGGG GAAGAGTGGT AGGAGGTGAA TCAGAGCGCT AAGACAGAGA 720 CAGATCGCCA AGGGCCTTTG GTGTGTATGC TGAGGAAGAA CGCTGTTGCC ATAGTTCCAG 780 TAAACAATGA TGGTGGCTCC GACCAACCAG TGGCACTGGC AGTGATAAGA GGGTCCACAC 840 ATCACTTCAG TGTAATAGAG CTCTAAGGTA GAAGTTTGAC ATTCAGAAAA AAGATGATGC 900 CTGAGCTGGG CGTGAACCAC GTGAAGAAAG TGGGAGGGAT GTTCCAGACA GGGGATCAGC 960 ACAATCAATG GCCTGGAGTC AGGATGGTTT CAAGGTAACT TCTAACAGTT TGGTACTACT 1020 AGAGTGTAAA GTTCAAAAAA CCTGGTGAGA GGCTGGCTGG GGCCCCATAG GCCCGCTTGC 1080 TGGGACTCTA GGGTTGCCAT TGAAGAGATT GAAGCAGGGG AGTGTTGTAG GTAGATGTGT 1140 TAGATTGGTT ACAGCACCAT AGAGGACTGA TTTAACAGGA GCCAGACTGG ACACGGTGAT 1200 TCTGGCAACC ATAGTTGAAG GGATATAGAA GAAGGATTGG GGGCCTGAAC TCTTGCAGTA 1260 GCCTCCTCCT CACTGGACCC TGTGGTCCAG AACACCTGCC TTGATCTGGC CCCTGGCACC 1320 TCTCTGACTT TGCCTTCTAC CACTCTGCAC CTCACTCTTC AGCATGGTGA TGGGGCCCCT 1380 GGTGGCCTAC CCCATGTCTT CTCTCCCCAG 1410
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