Tag | Content |
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EnhancerAtlas ID | HS110-04125 |
Organism | Homo sapiens |
Tissue/cell | KATO3 |
Coordinate | chr6:36650120-36651040 |
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 |
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| 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 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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Enhancer Sequence | GAGGGTGGAT AGAGGTTATT TGAGGGCTCT GTCCACTGTA CTGGGTGACC CCTTTATGGG 60 GCAGTGGCCT TTGGCCTTTT TAGCTGTATG ACTCAGGGGC AAGTCTCATA TCTCTTCCAT 120 CTCCTGCCCT TTAAACTTGG TGTGAAGTTA CCAAGAGCCT CCTCTCCCAA CCAGCTGGGA 180 CGTGAAACTG TGGGCTCCAC TGATCACAAG CAGTGGGGTG AGGTGGGGTG GAGCAGATGT 240 GGCATGTGTC CCGGGCTTCC TGCCTCATGA GGACTCAGCA GAGCTTTCAC CCCCAGAAAC 300 TGCAAGTTGG GACTTGTCCC TAGGAAAATC CAGTTGCTGC CAAGGTCGTG CAGTCACTCA 360 GCCCTGGAGT CAAGCCAGAG CAGGCAGGTA GGTGCCAGGG CTCCCTCATG GGCAAACTCA 420 CTCTCCGTTT TCCCTCTCCT GAAGGGGGAG GAGAGGAGCC AGGTAGACCA GCCACCTTTA 480 ATTTTCTTTT TGCCTGCAAA ACGGTTTCCT TGGACACAGG CAACACGAGG CAGGGGCTGC 540 CAGGTGTCTA GACTTCAGAT CACCTGATGT GCCTGGCAGG ATGTGGCTCA GCCTGGGAGA 600 AATCATCCCT TGCGCTGCCC CGCCCGGCCC CTCCTTACCC CTAGGCCACC CGCCTGACGA 660 CATCCTTGGG AAAGGCCCTC AGCCTACAGC ACCTGTCAGC TGCTGTCTGA AGGAGGTAGT 720 TGGCAGGGGG AAGTGATAGG GGGGAGGCTC AGTAAAACTG AAGGCAGAGA GGAATAATCA 780 TACTTCTGTT TTCAATGCAC TTCTCTATAC GAAGTGCTGC TGGCACGTTA CCTACATTAA 840 CTCAGTTAAT TCTCATGTCT ATCCTCTGAG ACAGTCACTA TTACTATCCC CATTTTATAG 900 ATGAGGAAAC TAGAGCTCAG 920
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