| Tag | Content |
|---|
EnhancerAtlas ID | HS091-24439 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr19:48293380-48294800 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chr19:48293807-48293826 | TTGCCACCAGGGGGCAGCA | + | 8.67 | | Foxd3 | MA0041.1 | chr19:48294282-48294294 | AAACAAACAAAC | - | 6.32 | | MEF2B | MA0660.1 | chr19:48294673-48294685 | GCTATTATTAGC | - | 6.07 | | Nr2f6(var.2) | MA0728.1 | chr19:48294402-48294417 | GAGGTCAGGAGTTCA | + | 6.22 |
|
| | 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 |
| GH19I047789 | chr19 | 48293254 | 48294310 |
|
Enhancer Sequence | TTTTTTTCTC TCTTTTTTGA GGACCATTGT GAACCAATGG ACTTTCATGC ATCTGACGTC 60
TTTCAATTCA TTGCAGCTCT TCTTTGTAAG CTCAAGTTGT TCAGCCTTTG GTTTCTTTTC 120
TTTTCTTTTA AAAAATATTA TTATAGAAAC GGGGTCTTGC TATGTTGCCT GGCTGGTCTC 180
GAATTCCTGG GCTCCGGCGA TTTGCCCGCT TCGACCTCCC AAAGCAGGAG GGGCTTTTGT 240
TTTATCCAAG CTCTCTGTCC CCGCCCCCTC CCCCAGTAGC CTGTCGGGTG TCTCCTGCCT 300
CCAAATCGGA TCTAATTCTC TCTCTGCTCT GCTGAGACTG GCCCTGGCTT AAGAGGACTG 360
GAACACTTGC TACATGGGAC CAGGACAGGG TCAGAGAACC AGCGCCGGGG AGACCCAAGG 420
GCCAGGATTG CCACCAGGGG GCAGCAGAGA GGCAGAGTAG CAGAAGGAAG AGGTGGGGGT 480
GCTTCCATCT GACGGCGGGC AGTGGGAGGG CGGGGTGGTG GATGAGGAGG GGATGGTATA 540
GAGGGAACAG TCCTCCCACC CCCACCAGAG TGGGTTAACA GTACTTACAT GGTCACTGGA 600
TGCGTATTGA AGAATGAGCC CGGGCTCAGT GATTCACGCC TGTAATCTCA ACACTGGGAG 660
GTTGAAATGG GAGGGTCTCT GGAGGTCAGG AGTTCGAGAC CAGCCTGGGC AATGTGAAAA 720
AACCCCGTTC CTACCAAAAA TACAAAAGAT TAGCCAGGCG TGGTGGCACG CGCCTGTGGT 780
CCCAGCCACT CGGGAGGCTG AGGTGGGAGG ATCCCTTGAG CCCAGGAGGT GGAGGTTACA 840
GTGAGCTGAG ATCACACCCA TTGCACTCCA GCCTGGGCGA CAGAGTGAGA CCCTGACTCA 900
AAAAACAAAC AAACAGACGA AAAAACAACA ACAACAAGAT AATTGAAGAA GATGTGGGCC 960
AGGCGAGGTG GCTCACGCCT GTAATCCCAG CACTTTGGGA GGCCAAAGTG GTTGGATCAC 1020
TGGAGGTCAG GAGTTCAAGA CCAGCCTAGC CAACATGGTG AAACCCCGAC TCTACTAAAA 1080
ACACAAAAAT GGCATGGTGG TACGTGCCTG TATTCCCAGC TACTTGGGAG GCTGAGGCAG 1140
GAGAATTGCT TGAAACTGGG AGGCAGAGGT TGCACTGAGC TGAGATCGCA TCACTGCACT 1200
CTAGCCCCTG GGTGACAGAG AGACTTCATC CCAAAAAAAA AAAAAAAAAG AGAGAGACTG 1260
ACAGAAAAAG ACCAAGAACA TTCTGTATGT GATGCTATTA TTAGCTATAA TAATGGCAGA 1320
TATGGTTTGT TGATCACTGA CCATAATCAG TGTTAAGATT TACATGATTT GACTCATCTA 1380
ACCCTTCTCC AAACCCTCCC TTTCACCAAA AAATCTTTCA 1420
|
