| Tag | Content |
|---|
EnhancerAtlas ID | HS034-10690 |
Organism | Homo sapiens |
Tissue/cell | ECC-1 |
Coordinate | chr16:376740-378200 |
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 | | Zfx | MA0146.2 | chr16:376900-376914 | GAGGCCGAGGCGGG | - | 6.01 |
|
| | Number of super-enhancer constituents: 4 | ID | Coordinate | Tissue/cell |
| SE_24104 | chr16:376670-376916 | Colon_Crypt_2 | | SE_24104 | chr16:377039-378284 | Colon_Crypt_2 | | SE_25025 | chr16:376637-376950 | Colon_Crypt_3 | | 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 | 376763 | 376865 | | chr16 | 377106 | 378041 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH16I000323 | chr16 | 373759 | 379105 |
|
Enhancer Sequence | AAAAAAAAAA AGTGATCAAA ATCAGGCCAC CGTCAGCTAT GAAAATCTCT ATTTTACTTC 60
CTCCATAAAA TCAGGGATGT GGCCTCTGCC TGAAGCGTCA GCCAAGATTG CCAGCACTGG 120
CCGGGTGTGG TGGCTCACAC CTGTAATCCC AACAGTTTGG GAGGCCGAGG CGGGGGGATC 180
ACGAGGTCAG GAGATGGAGA CCATCCTGGC TAACACGGTG AAACCCCATC TCTACTAAAA 240
ATATAAAAAA AATTAGCCGG GTGCGGTGGC GGGTGCCTGT AGTCCCAGCT ACTCGGGAGC 300
CTGAGGCAGA AGACTGGCAT GAACCTGGGA GGTGGAGCTT GCAGTGAGCC GAGATCGCAC 360
CATTGCACTC CAACCTGGGC GACAGAGCGA GGCTCCGTCT CAAAAAAAAA AAGATTGCCA 420
GCACCCCCAT CAGGTCCCAG AATACTCCAC CTACGTATCT CGTGGGTGTT CTGCATGGCG 480
GCAGACACTT GGTGTCACCC TCAGGGGCAG GAACAGGTGA TGGGCTGACC AGACAGCATT 540
GAATGACCAT GGGGCAGGGC ACTCTCACCC CTTCTGCTCA CACTGAATGA GCAGGTGATT 600
TCTCGGTCAC TCAGGGTGGC AGACACAAAA GGGCAAGAGA ATGAGTCACC AGGCACCAGG 660
CAGGAGCTTC CGGCTCAGCC CTGCGGCCTG TGCCTAGGAG GCCTCGCTGT GGTTCCACGC 720
TGCGGCCAGC CTTTTCTTTG TTTTATAACA CCGCTGGTGC CCCCACCCAC TCACTGTGAA 780
CCGCACAACA CACCAAAGGC CCTTTATGAT CAAAATCAAA CAGTGACGAT AGGGAGGGTG 840
TGTGTTTCTG CAGACTGTCC ACAGGCGCAG CACAGGCGGG GCAGCCCTGG CAGCCACCCA 900
CACCTGCCAT CCCGGGAGTC CAACAGCTCA AACTGTGGCC AAATGCCCCT CACCAGCACT 960
TACTGGCTAC TGACCACAGG CAGTCTGCCA ATTCCTAGCT TACAAAGCGG AAATGACAGT 1020
GGCCACTTCT TTATAAAGTT TCTGAGCATT TCAGCAAACA GTGCTTGGGT GAGGCCAGGC 1080
ACATGATGCA GAAAGCCCTC ACTACAGCCT AGCAACCAAA GTGTCCTGCA CATTAGTTAG 1140
GGGACTGGGT GGGAAAGGCT GCAGGTCACA GTTAAACCCA CAATTCCAAC TAACTGTCTG 1200
TGAGACTCTA AACAAATGCT TCACCAGGCT GGGGACAGTG GCTCAAGCCT GTAATCCGAG 1260
CACTGTAGGA GGCTGAGGCA GAATGCCTTA AAGCCAAGAG TTCAAGACCC ACCTGAGTGA 1320
AAAGGCCAGA CCTTGTCTCT ACAAAAAAAT GTTGCAAAAA TTAGCCAAGG GCTGGGCGGG 1380
GTAGCTCACA CCTGTAATCC CAGCATTTTG GGAGGCTGAG GTAGATGGAT CACTTGAGTC 1440
CTGGAGTTCA AGACCAGCCT 1460
|
