| Tag | Content |
|---|
EnhancerAtlas ID | HS158-13157 |
Organism | Homo sapiens |
Tissue/cell | Pancreas |
Coordinate | chr12:53358810-53359580 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ZNF263 | MA0528.1 | chr12:53359211-53359232 | GGAGGAGAGGGGAGGAGGTGG | + | 6.29 | | ZNF263 | MA0528.1 | chr12:53359208-53359229 | CGAGGAGGAGAGGGGAGGAGG | + | 6.41 |
|
| | Number of super-enhancer constituents: 4 | ID | Coordinate | Tissue/cell |
| SE_28333 | chr12:53358492-53359640 | Fetal_Intestine | | SE_28539 | chr12:53358261-53359767 | Fetal_Intestine_Large | | SE_43402 | chr12:53357688-53359860 | MCF-7 | | SE_47355 | chr12:53357831-53359332 | Panc1 |
|
| | 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 |
| GH12I052964 | chr12 | 53358092 | 53359764 |
|
Enhancer Sequence | TCTCTTTAGC CCTATTTTAG GAGCGAGGAA ATGAAGGAGC TGAGAGGTTA AGGGACTTGC 60
CCAGGAACGC CAGTTCGCCA GTGGCTTGCC AGGGATTTGA GCCTGGAGAG TCTCACTCTC 120
TGTCCGCATC TCAGTCGCGC TGATCTCGGC CACACGTAGG TCCATAGGCT GGTCCTCCCT 180
CACGAGTGGC CTCCGCGAGC CCCTGGCCCC TGGAGCGCCC TCCTCCCAGC CACCAGACCC 240
TCTGAGGCCT GACTCCTGGC TAGGCGGGGC TAAGGGGCGA GGAGAGCTGG GGGACAAAGC 300
CCCTTTACGT CGGGGTGGGA TTCCCCTTAA AGCCACTGCC AAGACGGAAC AGGATGGGGG 360
ACAGAGAGGG ACTGGGGGAA GGCGCCAAAG CCCGGGACCG AGGAGGAGAG GGGAGGAGGT 420
GGACTCTACT CGAGGGAGGA TCCGAGGGCG GGCAAGCGGA ACCCTCCTCC TTAAAGATCT 480
CGCAGTGAGG TTAGGGAGCT GCTCCCCGGC TCTGGGAAGC CGCTATCCTG CCCATACCCT 540
CCTTTCTCTC CGCTGCTGCC CCTGCCTCGC TCCCGCGCGC TCCCATTGGG TGGTGCCTGG 600
GTGTCCCCGG CTCGGCAGCT GCGGCTGCTT CCCAGCCCCG GGGTCTCAGG GCCGTCCCGC 660
CGGTCCCAGG GCACCGCTCC TGTGCCCCAC GCCGCCGCTT CCCCAGTTGC CCCCTGACTG 720
CAAGAGTCTC CTGGTTTTCG GCTTGTCCTG GGACTCCTGG GAGAGCCCAC 770
|
