Tag | Content |
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EnhancerAtlas ID | HS191-32594 |
Organism | Homo sapiens |
Tissue/cell | Trophoblast |
Coordinate | chr6:36650090-36650940 |
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 | ATATAAATAA ATCCCAACTC ATGCCTAGCA GAGGGTGGAT AGAGGTTATT TGAGGGCTCT 60 GTCCACTGTA CTGGGTGACC CCTTTATGGG GCAGTGGCCT TTGGCCTTTT TAGCTGTATG 120 ACTCAGGGGC AAGTCTCATA TCTCTTCCAT CTCCTGCCCT TTAAACTTGG TGTGAAGTTA 180 CCAAGAGCCT CCTCTCCCAA CCAGCTGGGA CGTGAAACTG TGGGCTCCAC TGATCACAAG 240 CAGTGGGGTG AGGTGGGGTG GAGCAGATGT GGCATGTGTC CCGGGCTTCC TGCCTCATGA 300 GGACTCAGCA GAGCTTTCAC CCCCAGAAAC TGCAAGTTGG GACTTGTCCC TAGGAAAATC 360 CAGTTGCTGC CAAGGTCGTG CAGTCACTCA GCCCTGGAGT CAAGCCAGAG CAGGCAGGTA 420 GGTGCCAGGG CTCCCTCATG GGCAAACTCA CTCTCCGTTT TCCCTCTCCT GAAGGGGGAG 480 GAGAGGAGCC AGGTAGACCA GCCACCTTTA ATTTTCTTTT TGCCTGCAAA ACGGTTTCCT 540 TGGACACAGG CAACACGAGG CAGGGGCTGC CAGGTGTCTA GACTTCAGAT CACCTGATGT 600 GCCTGGCAGG ATGTGGCTCA GCCTGGGAGA AATCATCCCT TGCGCTGCCC CGCCCGGCCC 660 CTCCTTACCC CTAGGCCACC CGCCTGACGA CATCCTTGGG AAAGGCCCTC AGCCTACAGC 720 ACCTGTCAGC TGCTGTCTGA AGGAGGTAGT TGGCAGGGGG AAGTGATAGG GGGGAGGCTC 780 AGTAAAACTG AAGGCAGAGA GGAATAATCA TACTTCTGTT TTCAATGCAC TTCTCTATAC 840 GAAGTGCTGC 850
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