| Tag | Content |
|---|
EnhancerAtlas ID | HS034-23985 |
Organism | Homo sapiens |
Tissue/cell | ECC-1 |
Coordinate | chr5:513440-514520 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| REST | MA0138.2 | chr5:513673-513694 | GTCAGCCCCATGGACAGTTGG | + | 6.18 | | SPI1 | MA0080.4 | chr5:513878-513892 | AGAATGAGGAAGTA | + | 6.18 | | SPIC | MA0687.1 | chr5:513878-513892 | AGAATGAGGAAGTA | + | 6.87 | | STAT3 | MA0144.2 | chr5:514214-514225 | TTTCTGGGAAG | + | 6.02 | | ZNF263 | MA0528.1 | chr5:513440-513461 | GAAGGAGAAAGGCCGGGAGGA | + | 6 |
|
| | Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
| SE_25092 | chr5:513376-515840 | Colon_Crypt_3 | | SE_27965 | chr5:513852-515901 | Fetal_Intestine | | SE_29117 | chr5:513814-515994 | Fetal_Intestine_Large |
|
| | 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 |
| GH05I000513 | chr5 | 513943 | 515785 |
|
Enhancer Sequence | GAAGGAGAAA GGCCGGGAGG AAGGCTGGCA AATGGCACAG CCGCTGTGCC GGGACGCAGG 60
TGCTAGATGG GCCTTCACAC ATGGGAGCCC CCACCCCCTG CTCTAACAGA GCTCAAGTGC 120
CCCCTAAAAG CACGTGGCCC CTCTGCGGAT GCAGAGTTGG GCGGGAGGAG AGCGCCAGGT 180
GCACGAGTGA TACCCAGGGT CTGTGCCACT GGGGTGTGCA GGGCAGAGAA CGCGTCAGCC 240
CCATGGACAG TTGGGTGGGT CCTGGCCACG GGGTCCCTGA GACACAGTGG ATGCTGAGAC 300
GGCCACGTCT GACTTCACAG CACACACATG CCACCTCCAT GGGACACACG TGCTCCTCAG 360
GGGCCCAGGG ACAGCTCTGG TGGGCAGACA GCAGCCCCGG GCCACCCTCG CCTTCTCCCC 420
CTGTGATGGT ACACAGTAAG AATGAGGAAG TAGTTCCTGA CAGCTCCTTC TCAGGAAGCT 480
TTAACTTCCC ACGGCCAGCC CTTGTGTTGC GGATTTAGGT CGAACGCAGC TCTCCCATTT 540
GTCAGCACCT CTGGCGACAG GGCTGCGCCC CAGGGCTCCT CTCCCTCTGA AGGCAGGCGG 600
GCCACGCACA GCCACTGGAG CTTCTCCTGG GAGCAGCACT CAGCCAACCC GAGCCAGTTC 660
CGCCTGAAGA GATTCCCCCA CTGTGTGCTG GGTGTGGGCG GTGGGCAAAA TCCAGAGAAG 720
CAGAGACAAT GGTGCCTGGC AAGGCCCCAG CCCCGGCTCG GGAGGGCACC CTGCTTTCTG 780
GGAAGAGATT ACTTCCCTAA TCACAGTTGG CTCTAACTAA TCCTAAAATG AACCTTCAGA 840
TCTTGAGAAA ACCAGGATTA AAGACAGAAA CCTGGAAGTG GCGCTCACAT GGGCGAGCCC 900
TCGGGGAGGC GTGCTCAGGC AGTCCCGGTT CCAAGACGCT TCACACACTC CCTCTTCCTC 960
CCTGACCTGA GGTCTCCCAG GCTCTGTGCC GCCAGGGCTG TCCCTCCAGG GGCTCTGTCC 1020
CTCAGGGGGC TCTGAGGCCC AGCCTCCGGC CTGTGCCCTC CCTCCTCACC TCTGCAGAGT 1080
|
