| Tag | Content |
|---|
EnhancerAtlas ID | HS091-45074 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr7:140143000-140144350 |
Target genes | |
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 | chr7:140143998-140144017 | CAGCGCCCCCTGCAGGTGG | - | 6.6 | | ZNF263 | MA0528.1 | chr7:140143712-140143733 | GGAGGAGGAGGTGGGGTGGAG | + | 6.83 | | Zfx | MA0146.2 | chr7:140144133-140144147 | GAGGCCGAGGCGGG | - | 6.01 |
|
| | 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 |
| GH07I140444 | chr7 | 140143841 | 140144070 |
|
Enhancer Sequence | TACTTAATTT ATCAACTATA TTTTGGAGTG TGTACTGTTT ATCATTCCTA TTTTTTAAAA 60
TGAAGCTATG AGACACAGAG ACATTAAGGT CACACAGCTA GTGAATGGCA CAGCCAGGAC 120
TCAAACCCCA CCAATCTGAT TCCAGAGTCC ACTTTTAACA ATTATGCTAG ACTGGAGGTG 180
GTGGCTCACA CCTGTAATCC CAGCACTTTG GGAGGCTAAG ACGAGAAGAT CACTTGAGGA 240
CAGGAGTTTG AAACTAGCCT GGCCAACGTG GTGAAACCCC GCCTCTACTA AAAATACAAA 300
AATTAGCCAG GCATGGTGGT GCCTGCCTGC AACTTCAGCT GCTGGGTAGG CTGAGGCAGG 360
AGAATCACTT GAATCCAGGA GGCGGAGGTT GCAGTGAGCC GAGATCGCAC TACTGCACTC 420
CAGCCTGGGT GAAAAAGCCA GACTCTGTCT CAAAACAAAA CAAGCAAATA AAGAAACAAA 480
AACAATTATG CTAAACTCCC TCTCAGATAA TGGCCAGCAC CAGATTTGGG CTCCATCATA 540
TTAACCCCTC ATCATTCTCA ACACACACAC ACACACACAC ACACACACAC ACACACACAC 600
ACACACACGA CAGAGAGAGA AATGTATCCA TTCCAAGATA TACCTCTCAT ACATGTATTT 660
CAGTGTCTTC CAAAGTAAAA TTGTGCAGCT GTCTGTAAAA GAAGCTAAAT AGGGAGGAGG 720
AGGTGGGGTG GAGAAGGGCT AGATGGCTGG GTGGAGTAGC CCAAACCCAT CTAACTGCAG 780
GAAAATCAGG GGGAAGCTGT GCTTGAAATG TGCTAGGCCC GGCCTGTGTA CACTTTCTCT 840
TAGATCATGA GGAAACTCCA GTTCACTCAG TGCAAGGTTA TTTGGGTGAG CCAGGGCAAA 900
TCAGGTTGAG CTCCACCCTA TCATCCGAGT CCAGGGGTTG GAATAGACAC TGGAAGGGAA 960
CGAGAGGTGG GGAAGGATGC AGCAAGGCAA GCACAGATCA GCGCCCCCTG CAGGTGGTTA 1020
GCAAAACTCC GGGTCATTGA GACGAGTTTC TGAGGATTCA TTATCGTCAA AGGCAATAAT 1080
AGAATTGGTT TGGCTGGGCT CCGTGGCTCA CACCTGTAAT CCCAGCACTC TGGGAGGCCG 1140
AGGCGGGCGG ATCACGAGGT CAGGAATTCG AGACCAGCCT GGCCAAGATG GTGAAACCCC 1200
CTCTCTACTA AAAATACAAA ACTTAGCCAG GCGCGGTGGC CAGCGCCTGT AATCCCAGCT 1260
ACTCGGGAGG CTGAGGCAGG AGAATCGCTT GGACCCGGGA GGCAGAGGTT GTAGTGGGTC 1320
AAGATCGCGC CACTGCACTC TAGCCTGGGC 1350
|
