| Tag | Content |
|---|
EnhancerAtlas ID | HS034-05244 |
Organism | Homo sapiens |
Tissue/cell | ECC-1 |
Coordinate | chr11:61467310-61468200 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Klf1 | MA0493.1 | chr11:61467960-61467971 | AGGGTGTGGCC | - | 6.32 | | ZNF263 | MA0528.1 | chr11:61467387-61467408 | GAAGGAGGGTGGGGCTGGGGA | + | 6.54 |
|
| | Number of super-enhancer constituents: 12 | ID | Coordinate | Tissue/cell |
| SE_23644 | chr11:61462269-61469316 | Colon_Crypt_1 | | SE_23957 | chr11:61465178-61468528 | Colon_Crypt_2 | | SE_25088 | chr11:61465275-61469220 | Colon_Crypt_3 | | SE_27201 | chr11:61461011-61469578 | Esophagus | | SE_29301 | chr11:61465002-61469417 | Fetal_Intestine_Large | | SE_41676 | chr11:61465207-61469249 | LNCaP | | SE_47728 | chr11:61465812-61468584 | Pancreas | | SE_51045 | chr11:61461234-61469434 | Sigmoid_Colon | | SE_57966 | chr11:61466379-61467907 | VACO_9m | | SE_57966 | chr11:61468067-61468448 | VACO_9m | | SE_63420 | chr11:61457154-61498627 | NCI-H69 | | SE_65661 | chr11:61460755-61471450 | Pancreatic_islets |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | GTGTTTGCTT TTCCCAGCCC TGCATTAGCT GTGCTGCTCA CACCTGGCTG ACTGTTTGCC 60
CAAGGATTTC TCCCCTGGAA GGAGGGTGGG GCTGGGGAGG GTGGCAGGCA GGTGGCCGGC 120
TGCCTCTGGG CACTCCGTTT TTCTGCAGAC CCACACTGCC TGCGAATGCC ACACCACCCT 180
GCATCCCCAA GGCTGCCCCA GCAGTGCCCG GCCTCGCCCG CGCAGAGCAT GTGACTTGGC 240
AGTGCCTGGG CCTGGCATGC CTGGCGTGCC AGGGCAGCGG CAGCAGCAGC CGGACTGTCA 300
GTAAGGAGCT GGAGAGGCCC CCAGAGCCCT CCTGTTGGGG CACTGGTCCT GGGTTGTGGG 360
GGTGACGGGA TGCATCAGTG AGACTTTTGT ATGGCAGGAG GCAGAGGAGC ACATAACTGA 420
ATCTGGGAGT ATTTATGGAC ACGTCTGCGC CTTCCTTTTC TGCAGCAGCC TGTCTGCAGG 480
CCCTCCTGCA AGGAGAGCCT GTCTTGATTC AACCAGTCCC TGCCCTGACC TTCTCTTCAC 540
CCTCTTTCTG ATGAGTCAGC CCCAGGAACT TGAACTTGGA CTTCTCCAGC CTCTGGGCCA 600
GCCCTGGAGG CGGAAGCCCT GGACCTGCCT CCCCAACACC TGCCCTCCTG AGGGTGTGGC 660
CTGCAAGCGT CCTTTTCTGT CAGATTCAGC TCATGGCCAG TGACTCCTTG AGCCTGTGAT 720
CGTGGTCCTC AGGCCAAGGG GAACAGATTA GATAATTAGC TGCTGATGGA TCTGGCATCC 780
TAGGGAAGAG GGAGCCCTTT CTCTCCCACA GCTGGGACCC CAAAGAGAGG CTTGCATTAG 840
CCAGGCAAGG AGCCGGGTGC CTCCCTCCCT GCAGTCCTGC ACAGCCCCTT 890
|
