| Tag | Content |
|---|
EnhancerAtlas ID | HS091-14286 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr14:105836950-105838100 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chr14:105837316-105837335 | CTGCCTGTAGATGGCGCTG | + | 6.36 |
|
| | 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 |
| GH14I105370 | chr14 | 105837241 | 105837418 |
|
Enhancer Sequence | AACCTAGTAG GCCAAGGCTG CAGTGAGTGG AGATTGAGCC ACTGCACTTC AGCCTGGGCA 60
ACAGAGCGAG ACCCTGTCTC AAAAGAAAAA ACTTCAAATC TCGGCTCACT GCAACCTCTG 120
CCTCCCAGGT TCAACAGGGT TTCACCCTGT TGGCCAGGCT GGTCTTGAAC TCCTGGCCTC 180
AAGTGATCTG CCTGCCTCTG CCTCCCAAAG TGGTGGGATT ACAGGCGTGA GCCACCGCGC 240
CCAGCCTTTG TTGTTTCTTT AACGTCAGAA GAAAAACGTG CCTGGGTTCA GGACCTGAAG 300
TGGAGAGGTG GCGTTTAAGC GTCTCAGCCT TGAAGCAGGG TTGTCACCCG TCGGCCTGAG 360
AGCACACTGC CTGTAGATGG CGCTGTGTCC TAACATACTC GGGATGCATC CAGCTCAGCC 420
CCTGGGGCAC ACACTCAGCG AGGCTGTCAG GTCCATGTGC CGAAACAGGT GCTTTGTGGC 480
CCGGTGGGGC AGGCAGCATT TCTGGGAACA GCGTAACATC ACCAACTGGC CGCAGAGGAA 540
GGGCAGCTCC GCCACTGGGA TGGTCATCGG GCCCCTGTGT CTTTTGGTTT GCATCTTGGA 600
TTGGAACATT CCCAAGTGCA GCTGAAGATG GGACTTAGCC AAGTCGGCTC CCTGGCCTGG 660
GGCTTCCTTG AGCCCTGCTG AGCGCCTGTG GGTTCAGGGG TGGGTGTTCT TGGTTGAATC 720
TTGACCGTGG GGTTCTGCAC TCACCTGGGC AACTGAACTG AGTCCCAGAA TGCATTTCAC 780
TTACACAGAT TATGGTTCTG AGACTCACAA CCCAAACTGT GAAAAGATGG GCCAACGTCA 840
CAGACGCTGT TCAGGGAGAG GACATCGTTT TCATAGGGAT AATTGCACAG CGTTGTGTGA 900
AATTCATGCA GGTCAACACA GTACTTTAAT GGAGTGATGG GATCTCTTTC CGTATTTTCC 960
ACCCATCACT CCCTTTCCTG AAAAGACCAG ACCATCTCCG CCACAGCTCT GAACCTGTGT 1020
CTTGGCCACT AGGAGTGCCA CACCTGGCAC TGCCCCCTGC CCAGGACTTC ACAGCAACCC 1080
TCAGGGGGCA GGAGATGCAC AGTGAGACGA GGTCACCGCC TGGATTACAG CCATCTGAGA 1140
TTGTTCATGC 1150
|
