Tag | Content |
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EnhancerAtlas ID | HS031-13865 |
Organism | Homo sapiens |
Tissue/cell | Denditric_cell |
Coordinate | chr20:23136400-23137890 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ESR2 | MA0258.2 | chr20:23137558-23137573 | TGGTCAGGGTGACCC | - | 6.33 | EWSR1-FLI1 | MA0149.1 | chr20:23136564-23136582 | GGAAGGAAGGAAGGAAGG | + | 10.83 | EWSR1-FLI1 | MA0149.1 | chr20:23136418-23136436 | AGAAGGAGAGAAGGAAAG | + | 6.16 | EWSR1-FLI1 | MA0149.1 | chr20:23136568-23136586 | GGAAGGAAGGAAGGTCTT | + | 6.26 | EWSR1-FLI1 | MA0149.1 | chr20:23136560-23136578 | GAAAGGAAGGAAGGAAGG | + | 9.6 | HNF4G | MA0484.1 | chr20:23136615-23136630 | TGGACTTTGGACTTT | - | 8.18 | IRF1 | MA0050.2 | chr20:23136543-23136564 | AGAAAGAAAAAGAAAGAGAAA | - | 6.27 | IRF1 | MA0050.2 | chr20:23136431-23136452 | GAAAGGAAAAAGAAAGAAAGA | - | 6.33 | IRF1 | MA0050.2 | chr20:23136549-23136570 | AAAAAGAAAGAGAAAGGAAGG | - | 7.14 | RARA(var.2) | MA0730.1 | chr20:23136857-23136874 | GGGTCACAGTAGGGTCA | + | 6.43 | SOX10 | MA0442.2 | chr20:23136400-23136411 | AAAACAAAGAA | + | 6.62 | ZNF263 | MA0528.1 | chr20:23136561-23136582 | AAAGGAAGGAAGGAAGGAAGG | + | 6.16 |
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| Number of super-enhancer constituents: 14 | ID | Coordinate | Tissue/cell |
SE_01996 | chr20:23136451-23137946 | Aorta | SE_09143 | chr20:23120940-23144036 | CD14 | SE_14768 | chr20:23127360-23138054 | CD4_Memory_Primary_7pool | SE_21001 | chr20:23136140-23138192 | CD8_Memory_7pool | SE_27325 | chr20:23136546-23137698 | Esophagus | SE_38349 | chr20:23136371-23137955 | HUVEC | SE_39918 | chr20:23135572-23137999 | K562 | SE_42509 | chr20:23136513-23137825 | Lung | SE_44389 | chr20:23136215-23138199 | NHDF-Ad | SE_46289 | chr20:23136168-23138340 | Osteoblasts | SE_51161 | chr20:23136223-23138019 | Skeletal_Muscle | SE_53897 | chr20:23136567-23137505 | Spleen | SE_56314 | chr20:23122847-23138372 | u87 | SE_67715 | chr20:23122847-23138372 | u87 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr20 | 23137375 | 23137725 | chr20 | 23136585 | 23137102 |
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| Number: 1 | ID | Chromosome | Start | End |
GH20I023141 | chr20 | 23121642 | 23143650 |
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Enhancer Sequence | AAAACAAAGA AAGAGAAAAG AAGGAGAGAA GGAAAGGAAA AAGAAAGAAA GAAGGAAAGA 60 AAGAAAAAAG AAGGAAAGAA AGAAGAAAGA AAGAAAGAAA GAAAGAAAGA AAGAAAGAAA 120 GAAAGAAAGA AAGAAAGAAA GAAAGAAAGA AAAAGAAAGA GAAAGGAAGG AAGGAAGGAA 180 GGTCTTAACA CCTTGGTAAT TTTTGTGCTC TTCCCTGGAC TTTGGACTTT GCAGCCTTAG 240 GGAGACAGAG CTCTTTAATG TACACTTTCC CATCAGGCAC TGCATGGCCA AGAACCTGCC 300 TGCAAAGCCC CCACTGAAGG GAGGGTTTCT CCAAGGAGCT CTCCCCTTTA AAGGCCCAGG 360 ATTGCTCCTG AGAGTGTCTA CTCTGCCATC AATACCATAA AGATTTCATC AGACGGCATG 420 GAGAGTGTTC AGTTGGGCAC TCTGGGTTGA GGGGTGAGGG TCACAGTAGG GTCATCTGGA 480 TCATTTCCCT GTCCCCCGGC CCCAGCTTGC TCCCTGATTG CATGTCATTT GACTCAGGCT 540 GAGCCTTGCA GAAGTCATAG CGGGGTGGAG ATGACTCACA CTATGTGGTT TTCCAACTGT 600 TGGGAGCAGC CAGGCAGGGT CCTTTTGTCA TGAGCAAGGC CATCGCCAAA TACACATTGG 660 CCAGGGTTCG ATGAAAATGT GAAAGTCTCA GCCCCATCAC TGGACTATGA CAGAAGCCTG 720 ACCAAGTATC CTTATCGAAA TGAAAACCTT TCATAGAGGT GGTTCTCCAC CTGTCAGGAG 780 TCACTGATCC TAACAGGGGC ATGAGAGCTG AAAGGAAACT TTCACAGTCA TTTAATATGA 840 CATCTTTGTT TTTCCCTTTC TTAGCATTTG TCCCGGGTCA CCTGGCTGGG GGTCAGGGGG 900 TACATAGGCC AGGATCCCAG CTATGACTTT AGGAATGCCT GAAGCTGGGG GGTGCTCGGG 960 CAGCAGGGAG GTGCTGAGGG TGACATGAGG GTGTACAGCA TGGCAGGGCA GCAGAATCAT 1020 CCCAGAAAGA GAGGATAGCC AAAGACATCG AGGCACAGGC GAGGTTGAGG AGCTTCGACA 1080 GTGGCCCTGA AAGGTGTATG GAGACCACGT TTCAGGACTT TGGCCACAGT GGAATCCCCC 1140 GACTGTTTTT GGGGACTGTG GTCAGGGTGA CCCGGCTGTG GCACATAGTG CCCAAAAACA 1200 GTTTCTCCAC ATCCCTGCAG GGCCTATCAG CCAAAATTTT AGCAGGCCTC AAGCCCAGAA 1260 ATCACTGGAA TTCAAGGCTC TTAAAAATAA TACTTGGCTA GGATACATGA CCACATGACA 1320 TTATTTCTAG TTAAATCAAA AGCTATTGAG GACCATGTCT ATTTTCATTT CATTTATACA 1380 GGGGAGGACA CCTCCCAGCA TCTGGGACAG AGGGAAGTAC ACGTCTTTAC AACCTTGGAT 1440 AAAAGTCATG TAACTCATGG CGCTTCACCT TTTCCCATGG CTGCCAGGGG 1490
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