| Tag | Content |
|---|
EnhancerAtlas ID | HS091-22844 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr19:2790630-2792350 |
Target genes | | Number: 12 | Name | Ensembl ID |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| MYCN | MA0104.4 | chr19:2791624-2791636 | GGCCACGTGGTG | + | 6.07 | | MYCN | MA0104.4 | chr19:2791624-2791636 | GGCCACGTGGTG | - | 6.07 | | NR2C2 | MA0504.1 | chr19:2791002-2791017 | TGAACCCTGACCCCG | - | 6.13 | | ZNF263 | MA0528.1 | chr19:2791146-2791167 | CCCTCAGCCCGATCCTCCTCC | - | 6.16 | | ZNF263 | MA0528.1 | chr19:2792043-2792064 | CCTTCCTCCTCCTCCTGTCCC | - | 6.27 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr19 | 2791617 | 2791719 | | chr19 | 2791953 | 2792056 |
|
| | Number: 2 | ID | Chromosome | Start | End |
| GH19I002788 | chr19 | 2788466 | 2790719 | | GH19I002790 | chr19 | 2790901 | 2791050 |
|
Enhancer Sequence | GGTAAGTCCC AGGCAGGGTC TGTGCGTGGG CCGCAGGTGC CGAGGGAGGT GGCACCGCAG 60
GCGGGAGTAG CCCAGCCCGT GGAGCCGGTT CAGAACCTGG CTTGAAGTGT CACCAGCACC 120
CTGCCCCTGA GCACAGGGCA GCGCCACCTG CTCCCAGGCT GGTCGTGGTG GCTAAATCAG 180
ATGGCTGGGC GGAAGCGTCT GGCAGGTGCT GGTCACTAGA GGTGTAGGAG AGAGGCAGTT 240
CCTCCCGTGC TCCGCTCTGC TTCACAGCCT CGTCCATTCA AAGGACTCCC TGGTTGTGTG 300
ATCTGAGAGC CGGAGATGAG AAAATATGTC TAAACAGCAC GCCTCTCCAG CCTCTCCCAG 360
AGCCAGCAGC CTTGAACCCT GACCCCGTCT GGCCTCTTTC CCTGGCCCGG GAAGGCGGGT 420
ATTTGTTTCT CTCTGAATGA CTGAACTTGG CCCCCTTGGC TTCTGCCTCT GCGCCCTCCG 480
GCGGGGGTGA CCTCATGTCC TCGGGCGTCC TCCTCACCCT CAGCCCGATC CTCCTCCTCT 540
CCTTGGGGTC CCTGTGCTCA CGGTGAGGAG TGAGGTGCCT AGTGACAGGG GTTAGGGACA 600
CTGCTTCCCG AGCTCTGCCT AAGGCTGACA GTGTACCTGC CTGACCAAGA GACCCAGAGA 660
GTCTCCGCAG AGAGCTCTGA GTGAGGCAAC TCCCCACCCT TCCATCTAGC GGAAGGCCTT 720
TTTGCTGGGA ACCATCGAGA ATCCTTGAGT TCAAGCCCAG GGCTTCTCTC GTGTTCCAAG 780
GCATCCCCTG AAAGGGTTGG CCTCCGTGGC CCATGCCATG AGGCCTCCAG AGGGTTTGTT 840
GTCTGGGCCA GGGGCTGGAG GGAGGGCTGA AGCTCCGCAA GCACCCCAAG CCTGCAGGTC 900
CCGCAGCCCC TGATTGGAAT CCTGACCCTC TTCCCACTCC CTCTGGCTTC CGACAAGTGG 960
CTTAGAGCCC GTATGACCTC GGTTTCCCCT CCTCGGCCAC GTGGTGGCCC CTTGTCCCTC 1020
CCGTAGGAGT CTCATGAGGC TCAGGTGATA CCAGTTCCCT CTTATGGCGC CCAGCGGTGC 1080
CAGGCATCAT TTCCCCCGCC CGTGCCCCAC CTTCCCCTCC TGCGGCCTTT CCTCTCCTCC 1140
TTCACATGGT GGCGAGACTA GCATTAAAGG AAACTGAATT CGGCCCCAGT GCTCCCCTCG 1200
GGGCCTTTCC GCTTCCCTCA GGGTGACGCC CAGCATCCTC GGTGTGGTCT TCAGCGCCCT 1260
GCACCGTCTG TGCCTGGACA CCCAGTCTCC TCGTGCCTGG CACCCTCCCC CAGCCAGGGC 1320
CTCTCCAGCC GGCCCCTCGC GCCCCTCGCC CTGTGCTCTG CTGAATGCCT GGCTTCTCTC 1380
TGATCACAGA TTAAGTCCAC TTCGCCCAGG AGCCCTTCCT CCTCCTCCTG TCCCCATGCC 1440
AGCTGCCTGG ATTAGTCCCT GCACGGTACT GACACTGTCG TCCCTGCGGT CACTTGTCTA 1500
ATCGGTCGCC CGTAAATCCC GAGAGGACAG AGCTGATTTT CTTTCTGTCT TCAGCCCTAG 1560
CGTCAGGCCT GGCCCAGAGC CCCCACTACA GGCTTTTTTG TTGTTTTTTT GAGACAGGGT 1620
CTTGCTCTGT CACCCAGGCT GCTGTAGTGC AGTAGTGTGA TCATGGCTCA CTGCAGCCTC 1680
CATCTCCCAG GCTCAAGCCA TCTTTAATTT TTGGTAGAGA 1720
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