| Tag | Content |
|---|
EnhancerAtlas ID | HS145-22288 |
Organism | Homo sapiens |
Tissue/cell | NHBE |
Coordinate | chr6:36650050-36650860 |
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 | TATTTTTAAA CTGCTTAGAA CAGCCCCCAA ACATAAAAAT ATATAAATAA ATCCCAACTC 60
ATGCCTAGCA GAGGGTGGAT AGAGGTTATT TGAGGGCTCT GTCCACTGTA CTGGGTGACC 120
CCTTTATGGG GCAGTGGCCT TTGGCCTTTT TAGCTGTATG ACTCAGGGGC AAGTCTCATA 180
TCTCTTCCAT CTCCTGCCCT TTAAACTTGG TGTGAAGTTA CCAAGAGCCT CCTCTCCCAA 240
CCAGCTGGGA CGTGAAACTG TGGGCTCCAC TGATCACAAG CAGTGGGGTG AGGTGGGGTG 300
GAGCAGATGT GGCATGTGTC CCGGGCTTCC TGCCTCATGA GGACTCAGCA GAGCTTTCAC 360
CCCCAGAAAC TGCAAGTTGG GACTTGTCCC TAGGAAAATC CAGTTGCTGC CAAGGTCGTG 420
CAGTCACTCA GCCCTGGAGT CAAGCCAGAG CAGGCAGGTA GGTGCCAGGG CTCCCTCATG 480
GGCAAACTCA CTCTCCGTTT TCCCTCTCCT GAAGGGGGAG GAGAGGAGCC AGGTAGACCA 540
GCCACCTTTA ATTTTCTTTT TGCCTGCAAA ACGGTTTCCT TGGACACAGG CAACACGAGG 600
CAGGGGCTGC CAGGTGTCTA GACTTCAGAT CACCTGATGT GCCTGGCAGG ATGTGGCTCA 660
GCCTGGGAGA AATCATCCCT TGCGCTGCCC CGCCCGGCCC CTCCTTACCC CTAGGCCACC 720
CGCCTGACGA CATCCTTGGG AAAGGCCCTC AGCCTACAGC ACCTGTCAGC TGCTGTCTGA 780
AGGAGGTAGT TGGCAGGGGG AAGTGATAGG 810
|
