Tag | Content |
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EnhancerAtlas ID | HS042-04866 |
Organism | Homo sapiens |
Tissue/cell | Fetal_brain |
Coordinate | chr10:17067200-17068300 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
RFX1 | MA0509.2 | chr10:17067775-17067791 | TGTTGCTATGACAACT | + | 6.38 | RFX1 | MA0509.2 | chr10:17067775-17067791 | TGTTGCTATGACAACT | - | 6.38 | RFX2 | MA0600.2 | chr10:17067775-17067791 | TGTTGCTATGACAACT | - | 6.26 | RFX2 | MA0600.2 | chr10:17067775-17067791 | TGTTGCTATGACAACT | + | 6.4 | RFX5 | MA0510.2 | chr10:17067775-17067791 | TGTTGCTATGACAACT | + | 6.21 | RREB1 | MA0073.1 | chr10:17068155-17068175 | CCCCAAACAACCACCACAGC | + | 6.67 | RREB1 | MA0073.1 | chr10:17068154-17068174 | ACCCCAAACAACCACCACAG | + | 6.73 | Stat6 | MA0520.1 | chr10:17067612-17067627 | TTTTTCCAGAGAAAC | + | 6.35 |
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| Number of super-enhancer constituents: 20 | ID | Coordinate | Tissue/cell |
SE_00693 | chr10:17064124-17068088 | Adipose_Nuclei | SE_02279 | chr10:17063748-17069478 | Astrocytes | SE_09959 | chr10:17063329-17070260 | CD14 | SE_12360 | chr10:17064454-17070140 | CD3 | SE_16659 | chr10:17064314-17070250 | CD4_Naive_Primary_8pool | SE_17226 | chr10:17064697-17070025 | CD4p_CD225int_CD127p_Tmem | SE_18814 | chr10:17064341-17074249 | CD4p_CD25-_Il17-_PMAstim_Th | SE_19922 | chr10:17064493-17072796 | CD4p_CD25-_Il17p_PMAstim_Th17 | SE_21442 | chr10:17066882-17070160 | CD8_Memory_7pool | SE_26240 | chr10:17064115-17068562 | Duodenum_Smooth_Muscle | SE_29863 | chr10:17067617-17068400 | Fetal_Muscle | SE_37595 | chr10:17064302-17069938 | HSMMtube | SE_38004 | chr10:17064380-17073255 | HUVEC | SE_44159 | chr10:17063596-17072780 | NHDF-Ad | SE_44819 | chr10:17063898-17069691 | NHLF | SE_45725 | chr10:17063483-17070392 | Osteoblasts | SE_47324 | chr10:17062926-17069482 | Panc1 | SE_55749 | chr10:17063010-17072777 | u87 | SE_63635 | chr10:17064588-17069776 | HSMM | SE_67629 | chr10:17063010-17072777 | u87 |
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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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| Number: 1 | ID | Chromosome | Start | End |
GH10I017021 | chr10 | 17063281 | 17072895 |
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Enhancer Sequence | TCTACTCAAT GAAAAGATGA TCGTTCAATT TTTGAGAACT ATACTCAATC AGTTTATAGA 60 GTGGCATTTT GAAGTGAGTG TCACTAATAG AAGATTATAT TTCAATCACA AGCAGGAAAG 120 CAATTTTATT GTAGAATGTA CTTGACTAAT GTCAATGTGG CCAGAGCCAG GCTCTGTGTT 180 CATAGCCCAG CTCTAAAATT TAGAGAACAC AATTTTGTGA AAATTATTGA ACTTCTTCAA 240 GCTAAAATGT CTTTATCTAT AAATCTGGCA CCATAATGGT ACTTATCTCA TAATATTGTT 300 GCCAACAGCA AATGAGATAA ACCACGTAAA AGGTTTGCTA TGAGGCCTGG CATGTGGAAT 360 GTGCTCAAAT TGTTACTCTA ACTCTTTGTC AGAGGCAAAG GGAATCAACA TTTTTTTCCA 420 GAGAAACCAC CCAAAATAGC TATGAGAAAA GAAAGATGTT GGGGATTAGA GAACAGGAGC 480 TGACTCACAT AAAAGAGTTC ACAGAAATCG TCACTGGTAG GGCAGATGGG GAAGTGATGA 540 ATTCAGTGAG GAGGTGGAGG CCAATCCTCG CAGTGTGTTG CTATGACAAC TTGGGCATTG 600 TGGAGACTGA GGCATCCCGG ACAGCCATGC AGAAACCAAG GCGAATCATC CTGTGTGGGG 660 TGGAGATAAG CATGCTGTGT GTGTGGAAGG GATTGCGGGA GGACAGATCA TGCAGGGGAC 720 AGCAGCAAAG AGAGTTAGGA AACCAGAGGC TGTTAAGGCT GCCACGGTGA GGTGGATAGA 780 GTCCACTGGC AAGCAAAGTG GCTCTCATGC TAAAAGTGAG CAGCATCTCT TCCTGTTGCA 840 GCCTCCCTTC CCCTTTGGGT CCTACCCAGC CCTGTAGTTC CTGCTGCTGA ATCACTGGAG 900 ATCCAGAAGG ATGGGACCTA GGGAATTCTC AGGGCATCTG CTCAGATGTT CCCCACCCCA 960 AACAACCACC ACAGCAGGAT CTGTGGAGAG GCCTCATTAG GGTGATTGTT AAAAATGTTG 1020 TTGCTGAGGT TTGCACTCAC ATCTCCTGGA AAAACTTGGA ACTTTATCCA AGTTCAGGTT 1080 ACTTTAAATT TGAAGGGCTT 1100
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