| Tag | Content |
|---|
EnhancerAtlas ID | HS184-26197 |
Organism | Homo sapiens |
Tissue/cell | T47D |
Coordinate | chr6:36650130-36650900 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| HNF4G | MA0484.1 | chr6:36650184-36650199 | TGGCCTTTGGCCTTT | - | 7.21 | | REST | MA0138.2 | chr6:36650144-36650165 | GGCTCTGTCCACTGTACTGGG | - | 6.23 | | TP63 | MA0525.2 | chr6:36650420-36650438 | TGCAAGTTGGGACTTGTC | + | 6.5 |
|
| | Number of super-enhancer constituents: 15 | ID | Coordinate | Tissue/cell |
| SE_09785 | chr6:36649543-36655272 | CD14 | | SE_10510 | chr6:36645365-36652556 | CD19_Primary | | SE_11108 | chr6:36644576-36654928 | CD20 | | SE_25216 | chr6:36650066-36651389 | Colon_Crypt_3 | | SE_27338 | chr6:36649190-36651696 | Esophagus | | SE_29503 | chr6:36649488-36651835 | Fetal_Intestine_Large | | SE_32367 | chr6:36649551-36652319 | Gastric | | SE_36489 | chr6:36643467-36652175 | HMEC | | SE_37550 | chr6:36642176-36651633 | HSMMtube | | SE_45438 | chr6:36650042-36650751 | NHLF | | SE_47969 | chr6:36650039-36650989 | Pancreas | | SE_53210 | chr6:36649506-36651969 | Small_Intestine | | SE_59249 | chr6:36634013-36660855 | Ly3 | | SE_64792 | chr6:36649495-36652124 | NHEK | | SE_65645 | chr6:36644736-36652645 | Pancreatic_islets |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | AGAGGTTATT TGAGGGCTCT GTCCACTGTA CTGGGTGACC CCTTTATGGG GCAGTGGCCT 60
TTGGCCTTTT TAGCTGTATG ACTCAGGGGC AAGTCTCATA TCTCTTCCAT CTCCTGCCCT 120
TTAAACTTGG TGTGAAGTTA CCAAGAGCCT CCTCTCCCAA CCAGCTGGGA CGTGAAACTG 180
TGGGCTCCAC TGATCACAAG CAGTGGGGTG AGGTGGGGTG GAGCAGATGT GGCATGTGTC 240
CCGGGCTTCC TGCCTCATGA GGACTCAGCA GAGCTTTCAC CCCCAGAAAC TGCAAGTTGG 300
GACTTGTCCC TAGGAAAATC CAGTTGCTGC CAAGGTCGTG CAGTCACTCA GCCCTGGAGT 360
CAAGCCAGAG CAGGCAGGTA GGTGCCAGGG CTCCCTCATG GGCAAACTCA CTCTCCGTTT 420
TCCCTCTCCT GAAGGGGGAG GAGAGGAGCC AGGTAGACCA GCCACCTTTA ATTTTCTTTT 480
TGCCTGCAAA ACGGTTTCCT TGGACACAGG CAACACGAGG CAGGGGCTGC CAGGTGTCTA 540
GACTTCAGAT CACCTGATGT GCCTGGCAGG ATGTGGCTCA GCCTGGGAGA AATCATCCCT 600
TGCGCTGCCC CGCCCGGCCC CTCCTTACCC CTAGGCCACC CGCCTGACGA CATCCTTGGG 660
AAAGGCCCTC AGCCTACAGC ACCTGTCAGC TGCTGTCTGA AGGAGGTAGT TGGCAGGGGG 720
AAGTGATAGG GGGGAGGCTC AGTAAAACTG AAGGCAGAGA GGAATAATCA 770
|
