| Tag | Content |
|---|
EnhancerAtlas ID | HS091-24688 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr19:54310920-54312480 |
Target genes | |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Nr2f6(var.2) | MA0728.1 | chr19:54312263-54312278 | GAGGTCAGGAGTTCA | + | 6.22 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH19I053808 | chr19 | 54312081 | 54312230 |
|
Enhancer Sequence | TGCTTGAAGG AAAGACAGGC CACTCTCTGG TGTTACTGGT GCTTGACAAC TATGGCCTTT 60
GCATGTCATT TCACCGTTTA TGAAGCATGC TATCCTTTTT TGAGACGGAG TTTCGCTCTT 120
GTTGCCCAGG CTGGAGTGCA ATGGCGCAAT CTCAGCTCAC CACAACCTCC GCCTCCTGGG 180
TTCAAGCGAT TCTCCTGCCT CAGCCTCCAG AGTAGCTGGG ATTACAGGCA TGAGCCACCA 240
CGCCCAGTTA ATTTTGTATT TTTAGTAGAG ATGGGGTTTC ACCGTGTTGG CCAGGCTGAT 300
CTCGTACTCC TGACCTCAGG TGATCTGCCC GCCTCAACCT CCTGAAGTGC TGGGATTACA 360
GGCGTGAGCC ACCACATCCG GCCAAAGCAT GCTATCTTTT CATTTTTTTT TTTAGAGGGC 420
CTTGCCCTGT TGTCTAGGCT GGAGTGCATG GTGAGATCAT GGCTCACTGT AGGCTTGACC 480
TCCCAGGCTT AAGCAATCCT CCCACCTCAG CCTACTGAGA AGCTGGGGCT ACAGGTGTGC 540
ACCATCATGA CCAGCTAATT TATTTTATAT TTTTAGAGAT GGGGATCTCA TCATGTTGTC 600
CAGGCTGCAC CTGGCTCTAT CTGACGCTCC TAATCATTGA TAGTTGGTTT ACTTGTTTCC 660
CTCTTTATTA TCTGTCTCCG TTCTCATTAG GATGCGTGCT CTCTTGGGAC CATTGGCTTA 720
TTCACACAGT CTTCTGTCTA CAGAAGATTG TTGGGTCCAC CGATAAAAGG GATATAGAGG 780
CTGGGTGTGG TGGCTCACAC CTATAATCCC AGCACTTTGG GAGGCTGAGG CCGAGAGTTT 840
GAGACCAGCC TGGCCAACAT GGTGACACCC CATCTCTACT AAAAAAATAC AAAAATTAGC 900
TGGGTGTGGT GGCACACTCC TGTGGTCCCA GCTGCTCAGG AGGCTGAGAC ACGCAAGGTG 960
GAGGTTGCAG TGAGCTGAGA TTGTGCCCCT GCACTCCAGC CTTGGTGACA GAGCCACACT 1020
CTCTCAAGAA AAAGGGACTT AGTAATATTT GTTGATTGAA TAAATTCTCC CAGACATCGA 1080
CCTCAATTTA GTCCCAATGG GTGTTGTTTA GTCTTTGTGG CACTATTGAC ACTTTGGGGC 1140
CAGAGGGACT GTCCTGTGTA CTGTAGGATG TTTGCAGCAT TCCCGGCCTT TATCCACTAG 1200
ATGTCAGTAG TATTATTTGC TTCCCAGTTG TGACCACCAA AAACGTGTCT CCAAACATCG 1260
CCAAATGTCA GAGCAAAATC ACCCCCAGCT GAGAGGCACT GGTTAAGAGC ATGAACCTCA 1320
AGGCCAAGGT GGGTGGATCA CTTGAGGTCA GGAGTTCAAG ACCAGCCTGG CTAACACAGC 1380
GAAACCCCAT CTCCACTAAA AATACAAAAA TTATCCTGGC ATGGTGATGG GCACCTGTAA 1440
TCCCAGCTAC TCAGGAGGCT GAGGCAGGAG AATCGCTTGA ACCCGGGAGG CAGAGGCTGC 1500
AGTGAGCCAA GATTGCGCCA CTGCACACCA GCCTAGGAGA CCAAGAGAGA CTTAGTTTAA 1560
|
