| Tag | Content |
|---|
EnhancerAtlas ID | HS091-09097 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr11:133796990-133799560 |
SNPs | | Number: 2 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CREB3 | MA0638.1 | chr11:133797663-133797677 | CTGCCACGTCACCA | + | 7.42 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr11 | 133797860 | 133798306 | | chr11 | 133798392 | 133798947 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH11I133927 | chr11 | 133797236 | 133799251 |
|
Enhancer Sequence | CCAAAAGAGA GAGACAGGAT AGGGGACGAG GGGCGGGGTG GGTCACACTG GAGAGAAGAG 60
GGTGCATGCA GGGTGCTCAG GGAGAAGGCA CTGGTGGGCC TGGCGTTCCT AGGTTCAAGG 120
GCAAGAAGAG GGCATGGCCC AGAGTGGATG CCCTGCCCAG CTTTGGCTGT GCCAATCCTC 180
CTGATGCTGG GTCACCAACC ACAGCTGGCA TCTTTTCTAC CAAAGGGGCC TTTAGGTGCA 240
AGTCGTGCTC AGGACACTGG TCAGATGGAT TACCAGCTGC ATTGTGGGAG AATCCCACCC 300
TGGTCACAAC CCTAAGAACA AGCTCTGCCT TGGGAGAGTA AGGCTCTGGG GTATGGGGAT 360
AAGCGGCTCA ACAGTGGCAG GATGAGGGAA GGAGCCCAGG ACCTGGCTGC ACACACCCCC 420
AGGGACAGCT GAAGTAGGGC CTCGGGTAAC CCACAGGGCT CATTCATCCA ATCAGACTGG 480
AGTCACCTGA GATGTCCAGG GTATAAGACC ATAATGACCA GGGGTTTCCC CACAGTGGGG 540
CCAGGATCCC TAAGGCCGTA AGGGTTGGAA GAAGGTCACG CTATGCATGG AGAGTAGGAA 600
GACGGGCCGA GGGTGTTCCC TTGTTCCACA GGCTCCCAAC TCCCAGCAAA GCCGGAGGGC 660
TATGGGTGCA GTGCTGCCAC GTCACCACAG GGAGGAGACA TGGTCCTGTG GGACTGGCCC 720
TCTCCTTGCA GCCCTGAGCT GTAACCTGGT GGGTGCCCTC CAGGATCCAC TCCCGGGTCC 780
CGGCTCACTA CCGTGCACGC CCAGGAGGGT GAGATGAGGC AGCGGAAAGC AGTACAAAAA 840
GAAGCCGGCG CCAAACGTCG GAGTCAGTGC ACAGAGTTAG AGGCAGGCAG AAAGAAAGGA 900
GACCTCCCCA ACCTCGGCCC CGCCCTTCCC TGGCCCAGGC AACAAAGCAG CGAGGAGCCA 960
CGTGTGGAAA AGCAGTGCAG ATGAGCAGCA GCGTGGAGCA GCAGCGTGAA GCAGCACCGC 1020
AAGCAGCAGG GGAGCCCCAA TCTACACCTG AGCCCCCCAT CGTATGCCCA GACCTCCCAC 1080
CCAGGCATCT CCAAAGACAG CTTGACCACA CCAAATGTCC CACCCTGGAC ACCTAGGCGC 1140
TGAGCAGCAC CGGTCTCCCA GCAGCCACCG GGCAGGCTGG TTAGGGCCCC CACGCTGCTG 1200
CGGGAGGAAC AGAGTAAGGG GACGGGAGGT GAGCTGCGGC AACTCCCATC ATCCAGGTGC 1260
AGTTCTCCAA TCAGAATCAA GACACCCAGG ACACTCCGCC CGGGAAGCAG CCACCGAACC 1320
ACCATGATGG GAGACAGAGC GGGTGCCCCT CTCAACTTCC CTCGCTGCTG AGAAGTGGAT 1380
AAAGGGGTCT CCCTGAACCC CCTGAGCTGC CCCAGGTGCC TGCCTTTTCC CCCTCCCCTC 1440
GAGCTCCCCC TCCTCGAGTT GAGCCTGGCT AGAGAGACAC CTGCAGGTGA GACAGGTCTA 1500
AAAGAAGGCA CTGAGGGGCT CGCCCTCCCA GCTCAAGGTT GTCACCCCCG GGGCAGGGCA 1560
GGTGGCTGCC ACTCTTACTC AAACAGGAGT GTAGGGAGGG GCAGCCCTTG GGGGTGGGAG 1620
GAGTCAGCTA GGCTTCCTTC TCCTCCCTTC CTGTGCCTCC TGCCCTCACC CCGCTTGGCA 1680
CATTTTTGAG ATCTGTATCT ACCCTAAGGT TTGCGCAAAG ACCTCATATG ACTGCATCTG 1740
GCTAAACTGA CAACAGAGGA ATGAAAACAA TCGAGAAACA CATGGTCCTA GAGAGAAAAT 1800
GCAGGGGCTG ACCCCAAGGC TGGGAAGTGA GCATCACCTC TCCACACCAG TTTCTGTGGC 1860
CTCTGGGGAA AAGACAGAAT AAAAACTAGA CTACAGGAGG TGGGGAGGGT GAACACGTAC 1920
AAATCATAGT GAGAAAGAAC CAGTAAGACC TGGTGTTTGC CAGCACAACA GGATTACAAG 1980
CAACAATAAT GTATCATACA TTCTTAAACC ACTATGAGTA TAATTGGATT GTTGGAACAC 2040
AAAGGACAAA TGTTTGAGGG GTGGATACCC CTTTACCCTG ATGCGATTAT TACACACTGC 2100
ATGCCTATAT CAAAATATCT CACGTACCCC ATACCTACAA ACGTATGTAC CATGTACCCA 2160
CAAAAATTAC AAATACAAAA ATACAAAAAA AATTAGTCTA AAAACTAGAC TCTACACTTA 2220
AGGCTGGGCA ATTTCACAAA GCCCTTGAAG GGCAGGAGTC TCTTCCAGGC TCCAGAGGAA 2280
TCCAGAGGAT GAAGCAGGAC GCAAAACGAG GCAGCACGTG AGCAGGGAGA GGGCACAGAG 2340
AGGCCCAGAC CCCTCAGGCC ACAGGGACAC AGCCATGCCC AGAGTCCCTT CAGACCCCTC 2400
CCGTCACCCA CAAGGACCTC ATCACTGTCT CAACCCACCT CAGTCTGTGC AGGGCTGGCA 2460
GGCCAGGAAC TGCAGCCTCC TCCTACCTCC CCCCACCCGG GGTAGCCTGC AGGAAGACCG 2520
GGGAGGGGAG AAGCAGAGAG CAAAGCATGC CGGGGTGACT CACAGAGGTC 2570
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