| Tag | Content |
|---|
EnhancerAtlas ID | HS052-32211 |
Organism | Homo sapiens |
Tissue/cell | Fibroblast_foreskin |
Coordinate | chr6:18362050-18363230 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| MEF2C | MA0497.1 | chr6:18362758-18362773 | TGTTTAAAAATAGAA | + | 6.11 |
|
| | Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
| SE_36128 | chr6:18361885-18362914 | HMEC | | SE_38461 | chr6:18361792-18363372 | HUVEC | | SE_59493 | chr6:18324545-18366590 | Ly3 |
|
| | 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 |
| GH06I018361 | chr6 | 18361906 | 18363293 |
|
Enhancer Sequence | AACAACAGAT GCATGTCTCC ACACCCAGCT AATATTTTGA TTATTTGTAA AAACGAGGTC 60
TCCCTATATT GGCCAGGTTG GTCTTGAACT TCTGGGCTCA AGTGATTCTG CCACCTTGGC 120
CTCCCAAAGT GCTGGGATTA CAGGTGTGAG CCACTGCGCT GTGCCTATCT TTCTTCTCCA 180
TTAACCTGCA GTAAATAGAG AATAAATTTT ACAGCATTCA TCATTTGTTT AGCTGGGTCC 240
CTGAACTTGC CTCCCTGGGA TAAGGCACCA TGACTGCACA GATCCAGCCA GATAATAGAA 300
GGTGTGCACT GGCTTCTCAC TGCATGGCTA TGTAGTGTAA TCACAGCGTG CCTTTGTGGG 360
GCTCCTGTTT ATGTGGCTTT AGTAGATGAT TTCATCCTCT TTTCTGACTT GGAACCAGAC 420
AACTTTACAT TCTCAGCAAA CAGATGGACA ACAGGGTTGA AATAAGATCT TGTACTGAAA 480
TAGTCCTTGA GTCATACTCC TTGACTGTTC TCTCATACGG GAAACTTGCC TCTTCCTTCT 540
TGCAGAAGGC CAAGGCTGAG AATTCAGTGT ACTCAGAGTT GCTGGACTCT TTTCTCAATA 600
TATATTATGT TGGATATTTT TCTTCTTGGT CAAGATTGAG AGTCTGCCAG TATAAGAATA 660
TTATCTAATT TGTTTTGGCA GAACACCTGG CCTTTTGCCC CAAGCAGATG TTTAAAAATA 720
GAACTAAAAG TTTTGCATTA ACTTGTTTTT GTCCTCTTTC CAAAAAAGAT CCTGACATGA 780
GAAAAAAGGG GAGCTTGATT TTACCTATGG TTTTATTTGG GAAGCAAGGG TGCTCTAGTT 840
CAGGGGTGTC CAATCTTTTG GCTTCCCTGG GCCACATTGG AAGAAGAAGA ATTTTCTTGG 900
GCCACACATA AAATACACTA ACATTAATGA CAGCCAATGA GCTAAAAAAA ATTGCAAAAA 960
AAATTGTATA ATGTTTTAAG AAAGTTTACA AATTTGTGTT AGGCTGCATT CAAAACCATC 1020
TTGGGTCACA GGGCTGCAGG CTGTACAAGC TTGCTCTAGC TGAAACTCAC CTGACTTGGT 1080
CATTGGCTTC TAGTGTACAT TGTGCCAGTA ACTGTGTGAC CTTGGGAAAG TCAGTTCGTC 1140
TTTCAATGCT GTTTCCCCAT CTGTAAAATG GGAGTGATAA 1180
|
