Tag | Content |
---|
EnhancerAtlas ID | HS098-22782 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr16:88803280-88803960 |
Target genes | Number: 13 | Name | Ensembl ID |
|
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
CTCF | MA0139.1 | chr16:88803891-88803910 | CGGCCACCAGGGGGCAGCA | + | 9.03 | KLF16 | MA0741.1 | chr16:88803919-88803930 | GCCCCGCCCCC | + | 6.02 | KLF5 | MA0599.1 | chr16:88803919-88803929 | GCCCCGCCCC | + | 6.02 | NFAT5 | MA0606.1 | chr16:88803485-88803495 | AATGGAAAAT | - | 6.02 | NFATC1 | MA0624.1 | chr16:88803485-88803495 | AATGGAAAAT | - | 6.02 | NFATC3 | MA0625.1 | chr16:88803485-88803495 | AATGGAAAAT | - | 6.02 | SP3 | MA0746.2 | chr16:88803918-88803931 | CGCCCCGCCCCCC | + | 6.11 |
|
| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_41570 | chr16:88803719-88807361 | LNCaP |
|
| 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 |
GH16I088737 | chr16 | 88803581 | 88804583 |
|
Enhancer Sequence | ACGAGGGCTC CGGCAATTGG GCTGACACCG TCCCTGAGCG TCAGGGATGG CCCTGCCAGC 60 ACCTGCCGTT CTCTGGGCCT CACTTTCCTT GAAAGGGTGG GAAAGGTGGC CCTGACCCCC 120 TTTCCAGCTC TGCGCACCTG AAGACTCTCA GGACCCCCAC CCCAGGGCCG TGGCTTCATT 180 TGCTTCATTC AGAAACACAT TGCAAAATGG AAAATCAAGG GTTAGGGTAA AGAAAGAAAG 240 TAGCCAGAAA GAGCCCCCAG GCCCTCCCAA GGCGACGTGG CCAACACAGA GTTCCCAGGC 300 CAGCCCCTGC CCTGGACGAG CGGCCTCCTG GGGCCACTGG GCCACCTGGA GCAGCTCCCA 360 GAGCTAACAG CACAAGACAG CATAGCCACA TTCTCTGGGG AGGGGTTGGG GGACCTGGAG 420 GCCCCCCATG GGGTCTTGGG GATCAACGAC GCGGCCACTC AGCTGCCCTG GGGGTCTTGG 480 GGGTTGGTCA GTGACATGGC CACTCGGCTG CCCTGGGGGT CTCGGGGGTC ACTGACACCG 540 ACCCGTGGAT GTCCTGGGCC CCCGAGGGGG CGGCAGGCAG AGGTGCGGCG CGAGCATGCG 600 AGAGCGCCAG GCGGCCACCA GGGGGCAGCA CCGGCCTCCG CCCCGCCCCC CGCACCCAGC 660 CATACCTTGC AGTGTGCGGT 680
|