| Tag | Content |
|---|
EnhancerAtlas ID | HS091-12514 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr14:23604580-23607120 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| BCL6 | MA0463.2 | chr14:23606283-23606299 | GTGCTTTCTAAGAACC | + | 6.26 | | HSF1 | MA0486.2 | chr14:23606662-23606675 | TTCCAGAACATTC | + | 6.62 | | ZNF263 | MA0528.1 | chr14:23605776-23605797 | GAAGGAGGGAAGGAGAAGGAA | + | 6.28 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_27342 | chr14:23606678-23608362 | Esophagus |
|
| | 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 |
| GH14I023137 | chr14 | 23606522 | 23608521 |
|
Enhancer Sequence | GAGCCACTGC GCCTGGACAT AAAAGTTATT TTTAAAAAGA AAAGTTTTAG GCCAGGTGCG 60
GTGGCTCACG CCTGTAATTC CAGCACTTTG GGAGGCTGAG GCGGGCGGAT CACGAGGTCA 120
GGAGATCAAG ACCGTCCTGG CTAACATGGT GAAACCCCGT CTCTACTAAA AATACAACAA 180
ATTAGCCAGG CGTGGTGGCA GGCGCCTGTA GTCCCAGCTA CTCGGGAAGC TGAGGCAGGA 240
GAATGGCGTG AACCCGGGAG GCAGAGTGTG CAGTGAGCCA AGATTGCGCC ACTGCACTCC 300
AGCCTGGGCG ACAGAGCGAG ACTCTGCCTT AAAAAAAAAA GAAAAATTTT AAGAGAATAA 360
TTTGAATGTT CCTAGCATAA AGAAAAGACA ATATTGAAGG AGATGGGATA TCTCAATTAC 420
TCTGATTTGA TTTTTACACA TTATATCAAT GTATTGAAAC ATCATCTGTA GCTTGAAAAT 480
ATGTACATCT ATTATATACA TATGAATATG AAACTTGAAC ATAAAAATCA GCCCTCCTTC 540
CCTTTTACTC TCCTAAGAGA AAAGTGAATA TTAGAAGCTG TCAACAGTAA TTTACATGTC 600
AGTGCAAATT GGACCACTTT TTTCTTTTTT CTGGGGAAAG GCCCACCTAA GGGATGACAG 660
GCAGGGTACA GCTTGATAGG AACAAAAAGG CACATATTCA GCACACTGGG AGTTCAGAGG 720
AGAATAGTCA TTTACTTTGT AATTTGTGTA TGGAGTAGAC TGAAGCGAAC AGCAGCAGCT 780
AATCAGAAGT GTGGGAGCTG ACTGTATCCC CAAGTACCCA TAAGCAGTAA CCATCATGAA 840
CTCCCTAGGC CGGTGTCACT AGTTTCATGC AGCCATACAC ATCCCTGTCC CCTCTCCCAT 900
GCTACTGCCC CTCTACAGGG CAGTCTCATG CACCAGGTGC TCTGTGGGGC TCATCGTGCA 960
CATAGCCAGG GTCCTGCACT CACGTCCCCC CTCCACATGC AGACAAGACC AAGTGTAATT 1020
GTCCAGATCC AACAGCATTT GCAAGTGTCA GGTTCACAAG AGACAGTCCT TGCCCAGCTA 1080
GCCGATAACG GAGGAGACGA TGACATTAAG CATAACACAC ATCCACACAC TCTGACTCTT 1140
CAGGAAGGAT CATCCTCTCC CTACCCGAGA ACACAAAGGA GTGACAGAGA GATAAAGAAG 1200
GAGGGAAGGA GAAGGAAGGA AGAAGGAACT GGAAAGATGA GCAGGGGAGG CCTGGGTGGG 1260
TGAGGTCTGG CCTCTGAATC GGAGGTGGAG CACACCATGC GCCACCGTTT CCTGCATGCA 1320
CACACGACTA GACCACATGC ACGCAGACCG CTGCTAGGCC TGCCTGAGGG ACAAACCCCA 1380
CTCTAAAGTG ACTGTAGCCA GTCACTCTCC TCCAATAGAT CTCAGGGAGC CTCACGGGTC 1440
ACTGTTCCTC CACCGCTTGG CCTCGGCGGG GCCTCCGTGT GGCCACTGCT CCTGTGTAAC 1500
ATGCACACGA GGTTGCTGTG GGTGAGCGTC ACAGGGTCCC GGGGTACAGG GGACACCCAC 1560
ACCACCTCTT TCCAGCCCTG GGTCCTAAAA ACATTGCACT CCCTTGTTAT TTCACAGGAA 1620
CTCTTCCTGA TGTGACGGCT TTGGAAGCAG CTGAACTCAC GGACTCATCT TTGGAGCAGG 1680
ACTGTACTTT CTGAGGGCAG GGGGTGCTTT CTAAGAACCT GGGAGGATCC CTTGAACCAC 1740
ACAAATGGAA GTCATTCAAC ATCTGCTAGC CTCAACAGCC CCTTCTGAAG ACAGCAAAAG 1800
AAAGGGCCGG GTCCCTGGAT GCATGGAGGC AGGACCTGGG ACTCGTGGAC CCGCTCGCAC 1860
TTCTGGCTTC TGAGAGTGCT CTGGGGTGGG GGTCACGGAT AAAAGGCTCT TTCTTTGGAC 1920
AAATGTTTGC TTTCCACTTT TCCCCACCCT CTCACTTCAC ATTCTCCACC TGAGTCTCAT 1980
GGGTGGCCTC AAAAAGGCCT CTACAGCCAC CTCTCTGTTG AGCAGGGAGG AGCTCTGCAT 2040
TCTTGGGGCA ATCAGGGTGA AGCCATCCCA CCTGCAGGCT AGTTCCAGAA CATTCATGGG 2100
AGGCCAGACC CAGAGGCCCC AGGCACAAGT CTCCCTCTTG GTCCCTTTCC AAATGGGGTT 2160
CTTTTCTAGC CAGCAGCAGC CTGTTTACAG GTACAGGACT GCAGCCAAGA TACTGCCTTG 2220
CTGCCAACCA CAGCCACTGA CTGGGGGCGG CGTCAGGCAG GCTGGCGGCC TCCTCTGTCT 2280
TCTGCTCCTT TTGAAATGAG ACAGGCCACT ACATGTGAAG CACCTAGGAC CCGTATGCCA 2340
CACACATCGC AGGTGACCAC GTGAGCAGCA CACACTCCTC AGCATCCACA CTGACACACA 2400
CGCCCTCATG TGAGCAGTCA CCCCTCTGCA AGCCCAACAT CCAGATGCCC ACACAGACCC 2460
CTGCTGACAG AGACAAGCCC ACCATATACA AATAGCAAAG TGCACAGCAG AGTGGCCCCT 2520
GGCCGGGGAA GGGCCCAGGC 2540
|
