| Tag | Content |
|---|
EnhancerAtlas ID | HS150-07834 |
Organism | Homo sapiens |
Tissue/cell | NT2-D1 |
Coordinate | chr3:141094140-141095250 |
SNPs | | Number: 2 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| MYC | MA0147.3 | chr3:141094328-141094340 | GCCCACGTGCCC | + | 6.44 |
|
| | Number of super-enhancer constituents: 6 | ID | Coordinate | Tissue/cell |
| SE_32498 | chr3:141094055-141096588 | GM12878 | | SE_43497 | chr3:141090170-141112703 | MM1S | | SE_52489 | chr3:141094170-141095457 | Small_Intestine | | SE_61127 | chr3:141079164-141144945 | HBL1 | | SE_62287 | chr3:141079553-141134828 | Tonsil | | SE_67139 | chr3:141090170-141112703 | MM1S |
|
| | 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 |
| GH03I141375 | chr3 | 141094056 | 141096588 |
|
Enhancer Sequence | TTAATGGCAA AGGTTGAACT AGACAAAGGG CCCAGAGTCA CCCAACCTTT AGGTAAGAGA 60
CAAAAGGCGC CAATGAGAAG ATTCACTCCT GAGGCAACGC CCTGCCTCAG CCAAGGAGCT 120
CTTACCTGCC CTCAGATAGG CATGCCCGTA CTTCAAGACA CTCTTGGGCA GCCTAGACCT 180
AGCAAGGGGC CCACGTGCCC ATCTTGGTCA CCTAATGGGG CCAGACTGTG GTGTGCCCTG 240
ATCCCTGAGG TGGTAGCACT GAAGAAGCTG GACCCAGGAG GACAGAGGGC AGCCGTGCAG 300
GCAGCATCCA TGTGATCAGC ATCACAAGAG CAGAGTAGGA GGTGGGATCT GGGGTCAGAA 360
ACCAAGACAG CGGAGCAGGG TCAGGGCAAG TGCCAGACTA AAATATGTGG GCAAATTTGA 420
GGTCAAGGCA GGGATGAGTT GAAAGGAAGA CAAGCAAGAG CTAGAGGGGA ACTGCTGAGG 480
ATTTGGCCTC AAGGATGGAG TCCCACTGTG TGACCTCACA GTCAGGGGAG GTACCTGCCC 540
CAAGCCGTGC CTGCCTTTTT AAATCTGAAA GGTGCTGTGT GCTGGGCTGC CTTCTGACAG 600
CAGGAGAGTA GGAGCACAGC CTGAGAGGCG GCAGGCCAGA GCAGGAGGAA CCTGAAAATG 660
GAAATTTAGG AAACAATGGA AAAAACAATT ATAGCAACAA AAAACCATTT TCTTTAAACT 720
CTCACCATCC TCTAAGAGGA AGTCTGACTA TTCATCCTGC CTGCATAACC CTGCTGAAAC 780
CCATCAACCC ACACCCACTG ATCACCTGAC AGTGTCTGAC TGCCCGGCTT CCTCTCATCC 840
CACCACCTCA ATTTCCAGAG CCCACCAAGG CATCACTTGA CTTTCAAGTT CTGCCTGGAC 900
AGACTGCTCA GCTCCCTACC CGCCCCAGTT CACGTTCAGG TTCTTGAAAT CAACTTTAGT 960
TTCCTCCATG CCTACATCTA TGCTGATCCC CTGCAAAGGC ACCTGGTGAC ACACAAGAGC 1020
CAGAACCCAA AGGAGCTCCT CCACAGGATC CTCCCAGGGC TTAGCCACCA GGGAATTTTG 1080
TTGATGATCC CCAAGCTTCA CTGCCCCATG 1110
|
