Tag | Content |
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EnhancerAtlas ID | HS116-03799 |
Organism | Homo sapiens |
Tissue/cell | Left_ventricle |
Coordinate | chr10:17067330-17068530 |
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 | GTAGAATGTA CTTGACTAAT GTCAATGTGG CCAGAGCCAG GCTCTGTGTT CATAGCCCAG 60 CTCTAAAATT TAGAGAACAC AATTTTGTGA AAATTATTGA ACTTCTTCAA GCTAAAATGT 120 CTTTATCTAT AAATCTGGCA CCATAATGGT ACTTATCTCA TAATATTGTT GCCAACAGCA 180 AATGAGATAA ACCACGTAAA AGGTTTGCTA TGAGGCCTGG CATGTGGAAT GTGCTCAAAT 240 TGTTACTCTA ACTCTTTGTC AGAGGCAAAG GGAATCAACA TTTTTTTCCA GAGAAACCAC 300 CCAAAATAGC TATGAGAAAA GAAAGATGTT GGGGATTAGA GAACAGGAGC TGACTCACAT 360 AAAAGAGTTC ACAGAAATCG TCACTGGTAG GGCAGATGGG GAAGTGATGA ATTCAGTGAG 420 GAGGTGGAGG CCAATCCTCG CAGTGTGTTG CTATGACAAC TTGGGCATTG TGGAGACTGA 480 GGCATCCCGG ACAGCCATGC AGAAACCAAG GCGAATCATC CTGTGTGGGG TGGAGATAAG 540 CATGCTGTGT GTGTGGAAGG GATTGCGGGA GGACAGATCA TGCAGGGGAC AGCAGCAAAG 600 AGAGTTAGGA AACCAGAGGC TGTTAAGGCT GCCACGGTGA GGTGGATAGA GTCCACTGGC 660 AAGCAAAGTG GCTCTCATGC TAAAAGTGAG CAGCATCTCT TCCTGTTGCA GCCTCCCTTC 720 CCCTTTGGGT CCTACCCAGC CCTGTAGTTC CTGCTGCTGA ATCACTGGAG ATCCAGAAGG 780 ATGGGACCTA GGGAATTCTC AGGGCATCTG CTCAGATGTT CCCCACCCCA AACAACCACC 840 ACAGCAGGAT CTGTGGAGAG GCCTCATTAG GGTGATTGTT AAAAATGTTG TTGCTGAGGT 900 TTGCACTCAC ATCTCCTGGA AAAACTTGGA ACTTTATCCA AGTTCAGGTT ACTTTAAATT 960 TGAAGGGCTT TGAAATGTTC CTGTAACAAC AGTAGAAATT GCAAAGCAAG AATCACAGAG 1020 GCTGGTTGTG GTGGCTCACG CCTGTAATCC CAGCCCTTAG GGAAGCCGAA GCGGGTGATC 1080 ACTTGAGGCC AGGAGTTCAA GACCAGCCTG GGCAACATGG CAAAACCCTG TCTCTACTAA 1140 AAATATAAAA AATTAGCCGG GTGTGGTGGC GTACGCCTGT AGTCCCAGCT ACTTGGAAGA 1200
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