| Tag | Content |
|---|
EnhancerAtlas ID | HS098-20952 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr16:1979150-1980260 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chr16:1979861-1979880 | GCGTGCCCCCTGCTGGTCA | - | 7.27 | | Myod1 | MA0499.1 | chr16:1979651-1979664 | TGCAGCTGCCCCT | + | 6.22 | | NRF1 | MA0506.1 | chr16:1979818-1979829 | GCGCCTGCGCA | + | 6.62 | | ZIC1 | MA0696.1 | chr16:1979807-1979821 | GGCCCCCCGCCGCG | + | 6.1 | | ZIC3 | MA0697.1 | chr16:1979807-1979822 | GGCCCCCCGCCGCGC | + | 6.63 | | ZIC4 | MA0751.1 | chr16:1979807-1979822 | GGCCCCCCGCCGCGC | + | 6.47 | | Zfx | MA0146.2 | chr16:1980188-1980202 | CAGGCCTGGGCCCC | - | 7.19 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_47923 | chr16:1979194-1979831 | Pancreas |
|
| | 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 |
| GH16I001928 | chr16 | 1978802 | 1980647 |
|
Enhancer Sequence | AAAAAAAAAA AAAAAAGAAA CAACCCCAAA CTGTAATTAT GATAAACAAC ACCGATCTCA 60
TTTATGGAGT AGGAAATCAA GCTGGAGAGG TGGGGTCAGC CTAGGTCAGA GCAGGCAAGG 120
ACTGTGGGAA CCTCTGAGGG AGGGACCTGG TCTGGTTATT ATTTTGCAGA GAGGACTCTG 180
GTTGGGGGAA GGCAGCCAGG AGCTGCCTGG GTTGTAGCGG GGAGAGGTGG GCGGAGGAAA 240
GAGGCCTGGG ATGTGGAACC CTAGGATCTA GCCCTGAGGG CGGGCCAGGT CCGGGCAGCC 300
TGGGTCCCAC GCAGCTGCCC TGAAGAAGGG GCTGGGGGCG TCCTGCCTCC ACCCGCGCCC 360
CCAACCACGC CTGCCGTTCC CACCGGCCGC GCCACCCCCG CCCCCGCCCC TGGCTCTGTC 420
CTCCGGTGAC CCTGGAAGGG GCACCCGTGG CTGCGACTGC ACTCCCTGTA GCGGTCACTT 480
CGTGAAGCCC GGCAAACCCC CTGCAGCTGC CCCTGGCACC CTCAGACGAC CAGAGGCCTC 540
GGCCTGGGTC CCCAGCACCG GCCCAAGGGC GGGCGTGGCC GAGGCGGTTT CTCTGCGCGG 600
ACGCTCGCTG CCTCCGCCGC AACCCCCGCG GCCACCCGGG GAACTGCAGC GCCGTCAGGC 660
CCCCCGCCGC GCCTGCGCAC GCAGACCACC CGGCCTGGCA GCACCGAGCG AGCGTGCCCC 720
CTGCTGGTCA GTCCTGCGCA CGGTCCCGCG CCCGGGCCCG GGAGGCCGCC TCGAGGGCCG 780
GGGCTTGCAC GTGGCCTCGG CGCCTTCGCC GACCCTACCG GACGCCCCCT CCTCCCACCT 840
GCCGACCCGT CCGCGGGTAG GAGCCTCCCG GGAGCTGCCC ACGGCCCCCA CCCCCACCAG 900
GGGCCACAGC CCCACCAGGG CCAGGCTCTG CGCGGCACCT GCCACTGAGA GAGCGGAAAG 960
CGGTGGTTGA GCAAGGGTCT GAAGTATGGT CTGTTCCCCC ATACGGGCCG CAGACGCTTC 1020
CTGGTGGCTG CTCTGAGCCA GGCCTGGGCC CCGGCGAGGG ATCACGGTGT CTCAGACAGA 1080
GTTCCTTTTT ATTCCCCATC CCTCGCCCGA 1110
|
