| Tag | Content |
|---|
EnhancerAtlas ID | HS112-03979 |
Organism | Homo sapiens |
Tissue/cell | KELLY |
Coordinate | chr12:120800940-120802130 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EWSR1-FLI1 | MA0149.1 | chr12:120801151-120801169 | GCCTCCTTCCTGCCTCCC | - | 6.08 | | EWSR1-FLI1 | MA0149.1 | chr12:120801155-120801173 | CCTTCCTGCCTCCCTCCC | - | 7.49 | | ZNF263 | MA0528.1 | chr12:120801330-120801351 | TTTTCCTCATCAGCCTCCTCC | - | 6.58 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_65438 | chr12:120798724-120802171 | Pancreatic_islets |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr12 | 120801471 | 120801881 | | chr12 | 120801931 | 120802027 |
|
Enhancer Sequence | GTTAGGGGAG GGAATGAGAA AGTGGGCATC TGAGTCCTGT GGCCTACCGC CACCAGCAGG 60
GGCTCGAGCC CCCCTGCCAG GATGCCAGCT GACAAGCTCT CTGTGGCCCC AGCCTCTTTA 120
AAGGCCCCCC CCCCGCAAGC TCCCTCTTGG ACCCCCGCCT CTAGGCCTGT CATGGGCAGC 180
TGTGCACCCA CACCCTGGCT GGCTCGAGTG TGCCTCCTTC CTGCCTCCCT CCCTAGGGAC 240
TATGTCCAGA AAATGCCTTC CCTAAGGACT AACACAGGGA AGGGGGCGGG CCAGTGACCC 300
AGACCCACAG CCTAACACTA AGACCTCACT GGCCCTCCTG GGAGACCCCC CAAGGTCCAT 360
CACAGAGTCT CCCTGAACTC AGTGCCGACA TTTTCCTCAT CAGCCTCCTC CCAACACAAC 420
CTCTGGCAGC CCTGTGGCCC CAGCCCTGTT TTAGGAAGAA CACATGGTCC TAATTACCCC 480
AGGAGCGCAT GGCTAATCCG CGGCAATTCC CAGCCCCATC CTAACACTAA AGCACCTTCT 540
GTCACCAAAC TGCTTAATGG AATTAACCCA GTTCCAACCA TGTGCTCCCT GGTGCGGCTT 600
CCTTCGAATA CCTGCTCCAT AATTGCTTTC AGGCCCTCTA CTGGACCCTT CCAGAGATGC 660
CCCTTTCCTG TCTCCCAAAA CTCTTCCTCT CCTTCAGCCC TGGCAGGAGT TGGGGGACTT 720
GATGGAATTC ACTGGCCCGG AATCTTAAAG AGCTCTAGTT CCACCTGGCA AAGGAGGAAA 780
CCGAACTCTC CTAGAGAGGG ACCTCGTCCT AGGACCCATG ATAAGTCAGT AAACTCAGGG 840
GTCCTGACCC CATGTTCCGC AATCAGTCTC TCCTTCTGTC CTCTATATTC AATTGCTTCA 900
AAAGGAAGAC CTGGCTAGTT GCCCTGAGGC CTAGAATAGA CTCTTAGGCC CCTGCCCTGC 960
ACCAAAAGTT TTTTGAGTGT TGTATCACTC AACTGCTCAG AAATCCATTT TCTGCGCACC 1020
TTGACCCTCT CACTGGGAGA ACTCGCCAGA GCAGCAGGGT AAGAGAGCAT TGAGAAAGCA 1080
GCCACAGACA TCTAAACTGA AAGACAACAG GTGACAGAGT CTGTGGTCCC CTCTGCCTCT 1140
GCAAAGGGTG ACTGGGGGGA TCCAAGGGTA GCTCCCTAGC CTGCCTGTAG 1190
|
