| Tag | Content |
|---|
EnhancerAtlas ID | HS118-17525 |
Organism | Homo sapiens |
Tissue/cell | Liver |
Coordinate | chr7:99618930-99621040 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| MEF2A | MA0052.3 | chr7:99619848-99619860 | TCTATTTTTAGT | - | 6.27 | | MEF2B | MA0660.1 | chr7:99619848-99619860 | TCTATTTTTAGT | - | 6.32 | | MEF2C | MA0497.1 | chr7:99619847-99619862 | TTCTATTTTTAGTAG | - | 6.57 |
|
| | Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
| SE_31872 | chr7:99619276-99622159 | Gastric | | SE_65863 | chr7:99619049-99622620 | Pancreatic_islets |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr7 | 99620111 | 99620161 | | chr7 | 99620306 | 99620683 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH07I100022 | chr7 | 99619941 | 99622370 |
|
Enhancer Sequence | GACGGGGTTT CACGATGATG GCCAAGCTGG TCTTGAACTC CTGACCGCAG GTGGCCCCCT 60
GCTCCCTGCC TCAGCCTCCC AAAGTGCTGG TATTACAGGC ATGAGCCACC TCACCCAGCC 120
CCAAGTTTCT AAAATGTGAA CATAGATGGG TTTTTCCTGG ATACTTGACA TCATTTTTGG 180
CAGTTAAATT ACATAACAAT GGAACCATTT CATACAGCTG TTCCTGTAAT TGCCCTTTCT 240
TCACACTTTC TTTAAAGAAG CTGATTACTC ATTGGTGACT TTTTCTTTGA TTTAGACTGA 300
CATTGGTTTT TACCTCCTAA TGTGGCTAAA ACCTTACTCT AGATAGAAGC TTCATCTGTG 360
CCATTTTCTT CTTGTTCACA TCTGTTTATA TTATTAGTGT GTCCTGTAAT TGCAGTTTCT 420
CTATAAGAAT CTTTTTTTTT TTTTTTTTCC TTTTCCTGAT AGGGCTTTGC TCTGTCACCC 480
AGGCTGGAAT GCAGTGGCGT GATCGTAGCT GACTGCAGCC TCAAACTTCT GGTTTCATGC 540
AATCCTCCCA CCTTAGCCTC CTGAGTAGCT GTGACTGCAG ACACAGTCCC CATGCCCAGC 600
TAATTTTTTT CTTTTTCATA GGGACAGGGT CTTGCTATGT TGCCCAGGCT GGTCTCAAAC 660
TTCTGGCTTC AAGCATCCTC CTGCCTCATC CTCCCAAAGG GCTGGAATTA TAGGCATGAG 720
CTACCATATC TGGCCACAAG AATCTTTAAA GCTGCTTGTC TCTTTTATGA CAGAGTCTCG 780
CTCTGTGGCC AGGATGGAGT GCAGTGGCGC GATCTCGGCT CACTGCAACC TCCGCCTCCT 840
GGGTTCAAGT GATTCTCCTT CCTCAGCCTC CCAAGTAGCT GGGACTACAG GTGCCCGCCA 900
CCGCGCCCAG CTAATTTTTC TATTTTTAGT AGAGACAGGG TTTCACCATG TTGACCAGGA 960
TGGTCCCGAT CTCCTGACCT CGTGATCCGC ACGCCTTGGC CTCCCAAAGT TTTGGGATTA 1020
TAGGCATGAG CCACTGCGCC CAGCCAAAGC TAGATTTAGA AATCCATTAT TTCACATAAC 1080
TGGTCTCAGA TAAACCAGTC TACATCACAA TGTCTAAAAT GAACAACACC TGTGACAGGT 1140
CAGCACAGAC TAAGTAAGTG TATTAGTGTC AATTTATAGC TTAATTTCTC TCTCTTTTAA 1200
GATACAGACA TTCCAATTAT TTTCTTTCTG TATCCTTTGC GGATCATCTT GTACTTTGGA 1260
AACCACAATT TAACTGCCCA AGTCACTCAT AAAAATAGCA AAAGTAGCTG GATGGTACAA 1320
AAGTAGGTCC CAGGGCTTCA AATTTGGTTG AATATTGACT CCAGTAGGCA GCCACCTACT 1380
ACTGAGCAAA CCTAACCCTC AGTTATGTCA TTTGTAAAAC AGCACTTAAC AGTTTGGCCG 1440
ACCTGCTAGG GCTGTTGTAG GGACAAAAGA AGATGGTGCG TGTACTGCTT TAAGCCTGGC 1500
ACCTGGCACT CTGCTAACAT TCAGCTCTCT GGGCTGGGCA CTGTTAATGC TCCATTTCGT 1560
AACCTGCTGT CAACCTGCAG GTAAATCACT CTGACTCCAA GCAAACACCC TGAGGGTGGA 1620
GTCGGCCTGT TTGAGGTTTC TGTTTGCAAA TCTTGATATA TGAAGTGACA GTGGAGATTG 1680
TACAGTTTTT TCCTCGATTT GTCAGGATTT TTTTTTTTTT GACGGAGTTT AACTTCTTGT 1740
CTCCCAGGTA GGAAGTGCAG TGGCGTAATC TCGGCTCACT ACAACCTCCA CCTCCTGGGT 1800
TCAAGCGTTT CTCCTGCCTC AGCTTTCCGA GTAGCTGGGA TTACAGGCGC CTGCCACCAT 1860
GCCCTGCTGA CTTTTGTATT TTTAGTAGAG ACGGGGTTTC ACCATGTTGG CCAGGCTGGT 1920
CTTGAACTCC TGACCGCAGG CGATTGGCCT GCCTCGGCCT CCCAAAGTGC TGAGATTACA 1980
GGCGTGAGCC ACCACCCCCG GCCTCAGGAG CGTTCTGATA GTGCCTCGAT GTGCTGCCTC 2040
CTATAAAGTG TTAGCAGCAC AGATCACTTT TTGTAAAGGT ACGTACTAAT GACTTTTTTT 2100
TTATACTTCA 2110
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