| Tag | Content |
|---|
EnhancerAtlas ID | HS007-06754 |
Organism | Homo sapiens |
Tissue/cell | BE2C |
Coordinate | chr17:2863090-2864320 |
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 | chr17:2863253-2863265 | ACTAAAAATAGA | + | 6.27 | | MEF2B | MA0660.1 | chr17:2863253-2863265 | ACTAAAAATAGA | + | 6.32 | | MEF2C | MA0497.1 | chr17:2863251-2863266 | CTACTAAAAATAGAA | + | 6.57 |
|
| | Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
| SE_31401 | chr17:2861487-2864472 | Gastric | | SE_65245 | chr17:2859093-2864439 | Pancreatic_islets |
|
| | 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 |
| GH17I002958 | chr17 | 2862229 | 2865246 |
|
Enhancer Sequence | ATTTCTTCAC TGAGGGGAGA AGGGGAAATA AAGATAATAC CCATTGTGGC CAGTTGCGGT 60
GTCTCACACC TGTCATCCCA GCACTTGGGA GGTCGAGGCA GGTGGATCGC CTGAGGTCAG 120
GAGTTCGAGA CCAGCCTGGC CAACCTGGTG AAACCCTGTC TCTACTAAAA ATAGAAAAAT 180
TAGCTGGGTG TGGTGGCACA CGCCTGTAAT CCCAGCTACT TGGGAGGCTG AGGCAGGGGA 240
ATCTCTTGAA CCCGGGAGGT GGAGGCTGCA GTGAGCCGAG ATTGCGCCAC TGCATTCAGC 300
CTGGATGGCA GAGCAAGACT CCATCTCAAA AAAAAAAAAA AAAAACAACA AAAAAAGACA 360
ATACCTCTAG CAAAATAGCA CATGGAGGAG AGAGGGCCCC GTGCTGGGCA GTGGCTCTGC 420
GGTAGGTTAT TAGGGGAGGG AGTGGCGTGG GGAGGGGATG GGAGGAAGTT TGCTCTCCTG 480
CCCTCGGGGC TGTTCCCAGA CAGGGATGAC TAATGCAGGC CAAACAAAAC AGACTCCTGC 540
CCTCACTGCC CCCACCCGCC ATCTGCCCAG TTTGCCAGCT GGGACAGGGT CTGTAGGGCC 600
ACCCAGGTGG CTTTGTGTGT GTGTGAGGGG AGCGCCTGTT CAGTGGGAAC GGCCCTCCCA 660
CGCCCTCCTG AACAATGCTG CAAGGCGACT CAGCCCAGGG AAGTCCGCAG AGGCTGCATG 720
TCAATCCACC CAGTTAACAG GAGCCCTGCT GTCCACAGAG TGTGGGGTAC GTCACGCGCT 780
TGGTGAGCCG GTGACCCGGC TTCAAATCTA GGCCCTGCCA CTCACTGGCT GTGTGACCTT 840
AGGCAAGCAG CCTCCTTCTG GGGCCCCAGT GTCCTCGCTG GTGGAAAGTG CTGTGAGTTT 900
CAAAGGAGGC CACAGAGAGA GCTAGCTTGG GAAGGTCAAA ATCCCTGTGC ATTAGTGTTG 960
TGACCAGGCA GACGCTGCTT CTGGACTCCT TCTGCTTCAG AGGGGACCTG TTTCTTCTAG 1020
TTTGTGTACC GTCTCATACT GTCACCCGAT TTTCTCAGAT AGTCTTGGAA ACACCACGTG 1080
TTCCCCTCCT GCACAACACG GTTAAGTCAG AACTCAGTGA TAGAACTGCT GGACCAGGGC 1140
CAGGCGCAGT GGCTCACGCC TGTAATCCCA GCACTTTGGG AGGCTGAGGC GGGTGGATCA 1200
CCTGAGGTTG GGAGTTCAAG ACCAGCCTGG 1230
|
