| Tag | Content |
|---|
EnhancerAtlas ID | HS091-10901 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr12:112817550-112819750 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| RUNX3 | MA0684.1 | chr12:112818702-112818712 | AAACCGCAAA | + | 6.02 | | ZEB1 | MA0103.3 | chr12:112819608-112819619 | CCCACCTGCCC | + | 6.14 | | ZNF263 | MA0528.1 | chr12:112819553-112819574 | CGAGGAGGGAGGGAGGGAGAG | + | 6.68 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | CCACACAAAC ACAAATCTAA TAGCCACAAA AACATTCTTA GCTATCTATT TCTCCTGATA 60
CCATGGAGCC TGTATAACAT GGAAAGAATG AAACAAGTTA TTCACTACTA CCAGTCATAA 120
ATGTTTATCA CCCATACACA TACTAGTTGC TGAGAAATCA GACCATAAAT TTAAAAAGCA 180
ATTAAAAAAA AAAATCTAGC AGGCCAGAGA GGTTCTTTCC TTTGAAAACC ATTCTTCTGT 240
GGAAATAGCT GACAAATTCA CGCAATACAT TTATAAACAT TTTAGGAAAA CCAACATCAC 300
AGATATTTTA ACTAATCCTA CTCTTTCTAA TCCTAAAAAT AAACTACATA AATGACATAT 360
ATGTATAAAT TTTGGTTCTG TGAACTTGGA TTAGTCTTTA AGAAACAAAG AGCATAGGCA 420
CGGCATAGTG GCTCACGCCT GTAATCTCAG CACTTTGGGA AGCCAAGGCA GGCAGATCAC 480
TTGAGGTCAG GAGTTCGAGA CCAGCCTGGC CAACATGGTG AAACCCTGTC TCTACTAAAA 540
ATACAAAAAT TAGCCAGGCA TGGTGGCGCG TGCCTGTAAT CCCAGCAACT CGGGAGGCAG 600
AGGCAGGAGA ATCGTTTGAA TCCGGGAGGC AGAGGCTGCA GTGGGCTGAG ATCGCGCCAC 660
TGCACTCCAG CCTGGGCGAC AGAGCAAGAC TCGGTCTCGG GGGAAAAAAA AGAAAAGAAA 720
GAAACAAAGA GCATCCACTT TCCACCTTTC ACACACAACA CAGCCAATTA AATCAAAAGA 780
TTCCACTATC ATAGCATAAT ACCCCTTGAG TTTTCAGGCA GATAAGACAC TCAGACACAC 840
CTTGCTTGTT ATAGAACAGG CCCAAATGAG ACACAATAAA ACGATGATTC CATGTTAGGA 900
ATTCCCTACC AACCATATCC TCCTCTTTTT GGTGACTAGA TTGTAAAATA AGTCAATTAA 960
GAGTTCATAA CGGAAGTGCT GAAGCAACCG CAAATCCAGA CACAAAAATA CAGTGGAACG 1020
TATTCGCATC TCAAGCACGT CCAAATGTCT CGGCCAATGT GATCCGATCA CTGCCGTTTC 1080
CAGAAACACA CAGTAATGGC TTTTAATTCA TTTCTATAAA TGTTCGTTGT GCGTAAAGCC 1140
AAACTGCACG CAAAACCGCA AAACACAAAA GATCCCTCGC ATGCCGTTTA TAGCCAGAAG 1200
ATAGGCCATC CTCTCTGCGC CCTACCCCAG AAAGCTCTCC TTACGGCAGT AAAAATTTGA 1260
TGACACCCCA TGCTACCTAC ACATCAAAAT GTCATCCCAC AAAGTGGAAG GGGAGCAGTG 1320
TCAGCATCCG TTGGCCTCCA TGAAACGACA CTGCCAGTAT TCCCACCTCT AGGCAAACAC 1380
GAACCCAAGT GAAGTCGATG GAAAGTTCCC ACCAACCAGG CATATTTGGT TCCCTTCTGC 1440
CCCCAAGGCC AAGCAGCTCA ACTGATGAGA TCTGCTGTTG CACCTGCCAC GGCTCTGAAC 1500
CCGGGATGCT TGGCGACCCC CGGGGCACAC AAAAAGGCCC TGCGGCCTAA CGCGCCAGTG 1560
ACCCTTCCCC GAGAGTGCAT GGAGGGCCGC TGGAGCATCC CTCTCGCTGT CCACAGCGCC 1620
CGCTTCCCTG ACAAAGGCCC CGTGTCAATC CATCCGAGAC ACAACACAGA GAAGTTGCTG 1680
GATTGCCCAT CGCGGACCCG CAGCTGCCAC TACCCTCTCC CGGAAAAAAA CCAAACCAAA 1740
CCAAACAAAA AAAACAGAAC TAGGGAAGAA AAGGATGGGA GGGTACACAG CGTGAAAATC 1800
AAAATGTTCC CAAAGCTAAG CAACCTGGGT GTGCCCTGGA AGTGGGTCCT GGGGGCCCGT 1860
GGGGGAGGGG AGGGAGGGCC CGGGTGGTGG CGGTGGCTCC TCTGGGGCAT GAAGGCCGAG 1920
CCAGGCGCTA GCCTAATAAA ATGCCGGGTG TCGGAACGCT CAAAAGAAAA CCACAAATGA 1980
AATCCCCTGC GGGCGCCAGG CCCCGAGGAG GGAGGGAGGG AGAGCGGGGC GGGCGGTCCG 2040
CAGACCTGCG GCCGCGGCCC CACCTGCCCG CCCCGCGCCC ACACACACCT GCCCCGGCAG 2100
CCGCCGGGAG GCGAGGCCGC GGCTGAGGCG AGGAGGGGGC CCGACCCGGG GGTGCCGGGC 2160
GAGTGGGTCA GTCCGATGGC GGGGGCCGGG GGCCGCCTCG 2200
|
