| Tag | Content |
|---|
EnhancerAtlas ID | HS099-08283 |
Organism | Homo sapiens |
Tissue/cell | HSMMtube |
Coordinate | chr16:377050-378320 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOS | MA0476.1 | chr16:377379-377390 | AATGAGTCACC | - | 6.02 | | SOX10 | MA0442.2 | chr16:377473-377484 | TTCTTTGTTTT | - | 6.62 |
|
| | Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
| SE_24104 | chr16:377039-378284 | Colon_Crypt_2 | | SE_25025 | chr16:377037-378435 | Colon_Crypt_3 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 3 | Chromosome | Start | End |
| chr16 | 377235 | 377950 | | chr16 | 377061 | 378314 | | chr16 | 377106 | 378041 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH16I000323 | chr16 | 373759 | 379105 |
|
Enhancer Sequence | AGACTGGCAT GAACCTGGGA GGTGGAGCTT GCAGTGAGCC GAGATCGCAC CATTGCACTC 60
CAACCTGGGC GACAGAGCGA GGCTCCGTCT CAAAAAAAAA AAGATTGCCA GCACCCCCAT 120
CAGGTCCCAG AATACTCCAC CTACGTATCT CGTGGGTGTT CTGCATGGCG GCAGACACTT 180
GGTGTCACCC TCAGGGGCAG GAACAGGTGA TGGGCTGACC AGACAGCATT GAATGACCAT 240
GGGGCAGGGC ACTCTCACCC CTTCTGCTCA CACTGAATGA GCAGGTGATT TCTCGGTCAC 300
TCAGGGTGGC AGACACAAAA GGGCAAGAGA ATGAGTCACC AGGCACCAGG CAGGAGCTTC 360
CGGCTCAGCC CTGCGGCCTG TGCCTAGGAG GCCTCGCTGT GGTTCCACGC TGCGGCCAGC 420
CTTTTCTTTG TTTTATAACA CCGCTGGTGC CCCCACCCAC TCACTGTGAA CCGCACAACA 480
CACCAAAGGC CCTTTATGAT CAAAATCAAA CAGTGACGAT AGGGAGGGTG TGTGTTTCTG 540
CAGACTGTCC ACAGGCGCAG CACAGGCGGG GCAGCCCTGG CAGCCACCCA CACCTGCCAT 600
CCCGGGAGTC CAACAGCTCA AACTGTGGCC AAATGCCCCT CACCAGCACT TACTGGCTAC 660
TGACCACAGG CAGTCTGCCA ATTCCTAGCT TACAAAGCGG AAATGACAGT GGCCACTTCT 720
TTATAAAGTT TCTGAGCATT TCAGCAAACA GTGCTTGGGT GAGGCCAGGC ACATGATGCA 780
GAAAGCCCTC ACTACAGCCT AGCAACCAAA GTGTCCTGCA CATTAGTTAG GGGACTGGGT 840
GGGAAAGGCT GCAGGTCACA GTTAAACCCA CAATTCCAAC TAACTGTCTG TGAGACTCTA 900
AACAAATGCT TCACCAGGCT GGGGACAGTG GCTCAAGCCT GTAATCCGAG CACTGTAGGA 960
GGCTGAGGCA GAATGCCTTA AAGCCAAGAG TTCAAGACCC ACCTGAGTGA AAAGGCCAGA 1020
CCTTGTCTCT ACAAAAAAAT GTTGCAAAAA TTAGCCAAGG GCTGGGCGGG GTAGCTCACA 1080
CCTGTAATCC CAGCATTTTG GGAGGCTGAG GTAGATGGAT CACTTGAGTC CTGGAGTTCA 1140
AGACCAGCCT GGACAACAAG GTGAGACCTC GTCTCTGCAA AATATTTAAA AAATTAGCCA 1200
GGTGTGGTGG CATGCACCTG TGGTCCCAGC TACTCAGGAG GCTGAGGCAG GAGGATCGCC 1260
TGAGCCCAGG 1270
|
