| Tag | Content |
|---|
EnhancerAtlas ID | HS051-28072 |
Organism | Homo sapiens |
Tissue/cell | Fetal_thymus |
Coordinate | chr9:139589890-139591280 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ZNF263 | MA0528.1 | chr9:139590031-139590052 | CCTTCCTCCTCCCCAGCCTCC | - | 6.86 |
|
| | Number of super-enhancer constituents: 9 | ID | Coordinate | Tissue/cell |
| SE_23641 | chr9:139589863-139590906 | Colon_Crypt_1 | | SE_23982 | chr9:139589880-139590638 | Colon_Crypt_2 | | SE_28198 | chr9:139587153-139591319 | Fetal_Intestine | | SE_29345 | chr9:139587045-139591372 | Fetal_Intestine_Large | | SE_41849 | chr9:139589832-139591298 | LNCaP | | SE_47596 | chr9:139587156-139591259 | Pancreas | | SE_62052 | chr9:139584688-139617720 | Toledo | | SE_65840 | chr9:139578814-139593075 | Pancreatic_islets | | SE_67135 | chr9:139579934-139591391 | H2171 |
|
| | 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 |
| GH09I136690 | chr9 | 139584563 | 139591452 |
|
Enhancer Sequence | AACACTTTCT TTAAATGACA TTAACCTCGC CCTGTTGTTG CTCAGTCACC TGTATAAATA 60
AAGGCAGACA CATTCTCTTG CCAGCACACT GCACTGCCCA GCACTGTGGG GCCTGGCTGG 120
GCACAGTGCC CGGGCCCTGG GCCTTCCTCC TCCCCAGCCT CCCAGAGAAC CCTGCTGAGA 180
GCACCTGGCT GCGGCCCTGG GGCGACGTCA GGTGGCTCTG TTTTCACGCC ACCTTCTTAA 240
TAAGCAGGCA GAAGCCAGGC GGGCCAGGAG AATGTGTCCT AGCCCGCAAG ACAGATGGTC 300
AAGAGGCCTG GCAGGAGCCC AGTGTCTGCC TGGTGAGACC ACAGCTGGTC AGGAGCCCAT 360
CCCCACAGGC CCAGGGTCAT GGTAGGCTGC ACCCCCTGGG GAAAGCCTGC CTTCAGGGAG 420
CTCGGCCTTG TGGGGGAGCC CCACACGTCC CCCCAGGCAG GCACCCGGGT CCTGATCCGT 480
CTGAGCTTTA GGTGAAACCC CCCTTCCCTC TGTGCATCCT GCTCCATCTC CTAGGCTCAC 540
CTTCTGTCGA GGAGGGCTGA GCGTCCCCCG CGGAGTCGAG CACAGCAGGG CCAGGATCTT 600
CTCAGGGACC CCCCGTGCCA GCTGCACGCA CGGCTCTCCG CAGGGCTGGT GAACCTGTTC 660
CCTGGAGGAA TTTACACACC ACGGGCTCAC ACGGCCAGTG CCGATGTGCA CTGCTCCCCT 720
TACGTGACAT GGGACGGTGA CAGGTGTTCG GCCGCCTGCT GTCTTTGCAC GTCCATGTGC 780
CCTGAGTGTC TCCGGCCAGG GCCACCTGGC ACCAGCTGCT GTCTGTGCCA CAGCACCGGT 840
TCTAACCAGC CCCGCCGAGG GGCCCCGGGC GCCCAGGAAG CCACACACCA ACACTCCCAC 900
CAAGGGCTGT GGGTTGCACA GACCAAGCCC AGAAGCCCAC GGGAGGGCAG GAGGTGACAG 960
ATGCTGGGAG GTGAGGGTCC CTGGGGCCCC CTGGGGCCTG GCCACCGCAC ACCCTGTAGG 1020
ACACACTAGG TCTAGACAGG TAGACTGTGA TTAAAACACA ATAGGAGGCC TGGAGATTCG 1080
ACCTGGTGCA GAACTTCCCT GGGCGACACC AGACCCTGCA ACACAGGCCC TCAGCAGATT 1140
CTCACCGCAG CCCCGACAGC AGGGTGGGCT CCAGGCTGTG CGGGTGAACA GCTGGGGTGT 1200
CAAGAGGAGG AGCTGCCCCT CCAAGTCACG TGGTTGAGGC CGTGCAGCCA GGACTGGGGT 1260
CTCCTAGGCC AGTCCAGGAC TCAGCTCTCC ACCACTGCCT GCACCTCCAC CCCCCAGCCT 1320
GGCGGAGCCT GGGGGGCCTG GGGCGCAAAT GAGGCCCAAA GATGTTTTTA TTCAGATTGC 1380
AAGATTCCTC 1390
|
