| Tag | Content |
|---|
EnhancerAtlas ID | HS091-13779 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr14:78282480-78284780 |
Target genes | |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ESR2 | MA0258.2 | chr14:78283920-78283935 | AGGTCACATTGACCA | + | 6.3 | | HES2 | MA0616.2 | chr14:78284766-78284776 | GGCACGTGCC | + | 6.02 | | HES2 | MA0616.2 | chr14:78284766-78284776 | GGCACGTGCC | - | 6.02 | | TFAP2C | MA0524.2 | chr14:78282727-78282739 | TGCCCCAAGGCA | + | 6.62 | | YY1 | MA0095.2 | chr14:78284462-78284474 | GCCGCCATTTTG | - | 6.92 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH14I077817 | chr14 | 78283761 | 78283910 |
|
Enhancer Sequence | GCTAATATTT TTTCAGGTGT TCCTCTGATT ATACTTTAGA AATACTAGAT TAGGAAATGA 60
AGGTTCCAAA GGGAAGAGCA ATGGAATTAT AAAAAAGGAC TATTGTGGTG TTATTATATA 120
TATTGGTTTT TGTCTGCTGT TCTTGGTTCA TAACTCCCAC AGCCCTTGTT ACGGTTTTTT 180
TTGGTGTGTG TTAGGCCTCA GGGCCAGGCC TTAGGAATCA GAATCTCTTT CCTGCCCTCC 240
TCTCACCTGC CCCAAGGCAG GATCGTGGTC TTTCCCCACC TTTCTGATTG TGGATCTTAA 300
CCCTCCCTAG AGTAGGTTCT GCCCTATACA CTGAGGGAAG GAATGCTGAT ATCATGAAGC 360
TTCCATAAAA ACCCAAGAAC CCAAGAGGGC TGATAGCTGA GCACTTGGAG ATTTGCGGAG 420
TGTGGTGCGC CTAGGGAAGT CCTGGAAGCT TCACGCCCTT TCGCTGTTAA CTGACCCTGC 480
ACATCTGTTA ATCAGTATTT TTTGCAGTCT CCTTTATAAT AAGCCAGCAA ACGTAAGTGT 540
GTACCTGAGT TCTGTGAGTT GCTGCAGCAG CTTGATCGAA CCCAAAGAAG GGGTTGTGGG 600
AACCCCAGCT TGAAGCTGGT TGGTCAGAAG TTCCAGAGAC CTGGACTTGT GACTGATGTT 660
GTGGGGGGAA GTGGGGGATG CAGTCTTGGG GACTGGGCCC TCAACCCATG GGATCTGACA 720
CCATCTCCAG GTAGTAGATG GTAAATATAT ATATATATAT ATATATTTAA AAAATGTGGC 780
TATATTATAA GGCATAAGTC AAAGTAGACT TTAAAGAAAA TGAGTAGGGC GTGGTGGCTC 840
ACACCTGTAA TCCCAGCACT TTGGGAGGCT GAGGCAGGCG GATCGCCTGA GGTCAGGAGT 900
TTGAGACCAG GCTAGGCAAC ATGGCAAAAC CCTGTCTTTA CTAAAAATAC AAAAATTAGC 960
TGGGCATGGT GGTGGCCACC TGTAATCCCA GCTACTCGGG AGGCTGAGGC AGGAGAAACG 1020
CTCCAACCTG GCAGGCGGAG GTTGCAGTGA GCCGAGATCG CGGCACTGCA CTCCCGCCTG 1080
GGCGACAGAG CAAGACCCTG TTTCAGAGAC AAATAAAATG AAGATAAGCT TGTTTGTAAT 1140
AATAGTTTCC ATACAAAGGG GAAACAGGCA CAGAGCAGGG AGGTGACAGG CACAGACTCA 1200
TTCCAGAGCA GAGGGATGAG GGTACAAGGC GTGCAAGGCT GGTGCCTGCA AGTGGCTTGG 1260
TGGCGTGCTG CTGCTCTCGT GTGGCACTTC TCTCCTGGCA GCTGCAGCTG TGGTCATGGA 1320
CTTTAGTCTG ACATAAATTG CTCAGGAATT GAAGGGGAAG CACTCTGTTG GGTGCACTGG 1380
CCGCAAAGAG TGACTGTGCA GCCACCTGGT GGACTGAGCA GGTACAAGTA GGGTGGGGAA 1440
AGGTCACATT GACCAGGAGT ATGAATTTGA ACAGATCAAA TCAGCAGGTA GGCATTAAGC 1500
CTCTAACTGT AAAAAACTCC ACAGGACTGT GAGTGGGCAG AGTAGTGACA GTCATAGTGT 1560
CTGCCCTCAA GGAGCCTCCA TTCAAGACAA GGGGTAGTCT TCTTTTTTTT TTTTTTGAGA 1620
CGGAGTCTCG CTCTGTCACC CAGGCTGGAG TGCAGTGGCG CAATCTCGGC TTACTGCAAG 1680
CTCCGCCTTC CGGGTTCACG CCATTCTCCT GCCTTAGCCT CCCGAGTAGC TGGGACTACA 1740
GGCGCCCGCC ACCACGCCTG GCTAATTTTT TGTTTTTTTT TTAGTAGAGA CGGGGTTTCA 1800
TCGTGTTAGC CAGGATGGTC TTGATCTCCT GACCTTGTGA TCTGCCCGCC TTGGCCTCCC 1860
AAAGTGCTGG GATTACAGGC GTGAGCCACC ACGCTGGGCC TCAAGGGGTA GTCTTCTCTA 1920
ACCAAAGTAA ATGTTTTGAA AATCAACCAT ACACAGAGGG CTCACCTGGC TGCTCCTGAG 1980
TAGCCGCCAT TTTGGCTGTG GCCTGACCAC TTTTGACCTG AGTGTAGTGG GCTAGTGATG 2040
CCTGTATGTG CATTGTGGTA TCATGATAGA CACAGTAGCA ATGGTTAACC TGCTCTTCTG 2100
CTTTGCTTCT AAAATAACAT TCTTCCTCTC TCCTGATCCC TTAGCCCTCT CTGCTTTTTT 2160
TTGAGACAGG GTCTGGCTCT GTCACCCAGG CTGGAGTGTG GTGGCACGAT CTCAGCTCAC 2220
TGCAGTCTCC TCCTCCCGGG CTCAAACCAT CCTCCCACCT CAGCCTCCTG AGTAGCTGGG 2280
ACCACAGGCA CGTGCCATGA 2300
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