| Tag | Content |
|---|
EnhancerAtlas ID | HS091-09815 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr12:49457080-49458460 |
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 | chr12:49457878-49457897 | TGGCCACTAGAGGGTGGTG | + | 7.07 |
|
| | 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 |
| GH12I049063 | chr12 | 49457584 | 49458183 |
|
Enhancer Sequence | CCAGAAGAAC CTCCTAAGCC AGTGAGATTG TTGTTTGGAG TATGTTTCTT CTAGCAGCCC 60
TTATTTCTTT TTAGATTCTG GATCAGAAAA GCAAAAGCAG CTGTCAGGAC TTTTGAAAAT 120
CAGCATGACA AGCCATATCC CCAACTGTAA GCCTGGAGCC AGGCACTGAC AAAGTCACAG 180
CTAAAAATCA CATCTAGGTT TTGTCAATCC TTCCCAAGTA AGTACATTGA TAGGGTACCT 240
CGGGCTCCCC CAGTTGTCAG AAGAGGTCTG TACCTTCTCT GTGAAGATCT ACCATTCAAA 300
TAACCCTTAC ACATCCTTGG AGGAGGTATT AGACTAGTTA GGCAATCAGG CTGGTGGGAG 360
GGTGGGGATC AAGAAAAGCA GAGGCAAACA GGACCAAACT TTCCTAGCTG AAATATCAAT 420
TCATTGAGGC GGTAGGCCCA TAAAAGCAGA ACCAATAGCC TTTGACACCT AAAAAAAAGT 480
AGCACACCAC CAAAGGTGTA AAAAGTACAA AAAGATTAAA GGTATGAAAA CAGCAAAGAA 540
CGGCCATTTT AATGGAAGAC ACTGGGGACA TGGAGGGCCA GGGGACTGAT ATGCACCGGA 600
GGCATTATTT CTTACTTTAC TCAACACTCT TGGGAAGTCA AAGTCTTCAC AACACTTTAG 660
TCTCTGCCTC TACACTCCTT CTCAATTCTT ACATCATTAG GAATGAGGGG CTTCCTTTCT 720
TCTCCTGAAA CCCCATCATC TTTGAATCCA AGCAAATGCC GAGGCCCCAG GAAGACAGCT 780
AGGTCAGCAT GTTGCAGTTG GCCACTAGAG GGTGGTGTTT CTGTAATTAA GGGGATCTTG 840
AAAGGCTACA AAACTTGGAT GGGAGTGGCA GCCAACTGGA CTTAGTATAT GAGGAACCCA 900
GCAGAATAGA AAGGTGGGAA AGGCAAGTAG TAAATCTTAG GATAATGGTC CTTAATAAGT 960
GAGGAATAAG GAATAGGAAC AAGGTAGGAG GAAAGATATC CCACCAAAGA CCACAGCCAT 1020
CACTCCTTGG AAAAAGAGAT CTTGGCTCTG AGCTCTCACT AGATACATAG AAGTCAACAA 1080
TAAAATAAGG CCGGGGGCAG TGGCTCACGC CTGTAATCCC AGCACTTTGG GAGGCTGAGG 1140
TGGGTGGATC ACTTAAGGTC AGGAGTTCGA GACCATCCTG GCCTAGGTGA AACCTCATCT 1200
CTACTAAAAA TAAAAAAGTT AGCTAGGCAT GGTGGCGGGT GCCTGCAGAA GACTGAGGCA 1260
GGAGAACTGC TTGAACCTGG GAGGCGGAGG TTGCAGCGAG CCAAGATTGC AGCACTGCAC 1320
CACTCCAGCC TGGGCAACAG AGTGAAACTC CGTCTCACAC ACACACACGA AAAAGAAGTC 1380
|
