Tag | Content |
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EnhancerAtlas ID | HS195-00403 |
Organism | Homo sapiens |
Tissue/cell | VCaP |
Coordinate | chr1:154390120-154391670 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chr1:154390884-154390902 | GGATGGGAGGAAGGCAAG | + | 6.39 | ZNF263 | MA0528.1 | chr1:154390963-154390984 | GGGGGAGGAGGGAGCAGGGGC | + | 6.21 | ZNF263 | MA0528.1 | chr1:154391457-154391478 | GGGAGAGGGGGAGAGAGAGGG | + | 6.21 | ZNF263 | MA0528.1 | chr1:154391432-154391453 | AGAGCAGGGAAGAGGAGAGGA | + | 6.23 |
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| Number of super-enhancer constituents: 33 | ID | Coordinate | Tissue/cell |
SE_00437 | chr1:154390273-154397370 | Adipose_Nuclei | SE_01040 | chr1:154390266-154394476 | Adrenal_Gland | SE_06653 | chr1:154390374-154394420 | Brain_Hippocampus_Middle | SE_09189 | chr1:154388527-154398657 | CD14 | SE_14719 | chr1:154390449-154393846 | CD4_Memory_Primary_7pool | SE_16173 | chr1:154390869-154392998 | CD4_Naive_Primary_7pool | SE_17632 | chr1:154390245-154394418 | CD4p_CD25-_CD45RAp_Naive | SE_18405 | chr1:154389059-154394421 | CD4p_CD25-_Il17-_PMAstim_Th | SE_19165 | chr1:154390146-154394423 | CD4p_CD25-_Il17p_PMAstim_Th17 | SE_24531 | chr1:154390928-154392675 | Colon_Crypt_2 | SE_26130 | chr1:154390648-154394176 | Duodenum_Smooth_Muscle | SE_26877 | chr1:154390381-154397107 | Esophagus | SE_32086 | chr1:154390256-154393099 | Gastric | SE_36673 | chr1:154390756-154393680 | HMEC | SE_41139 | chr1:154390423-154394426 | Left_Ventricle | SE_41647 | chr1:154390541-154393000 | LNCaP | SE_42431 | chr1:154390433-154394432 | Lung | SE_43544 | chr1:154384840-154394484 | MM1S | SE_44716 | chr1:154390741-154394024 | NHDF-Ad | SE_47983 | chr1:154390623-154393036 | Pancreas | SE_48261 | chr1:154388323-154397557 | Psoas_Muscle | SE_48934 | chr1:154390514-154394206 | Right_Atrium | SE_50453 | chr1:154390541-154394239 | Sigmoid_Colon | SE_51380 | chr1:154389216-154394408 | Skeletal_Muscle | SE_52880 | chr1:154390698-154393024 | Small_Intestine | SE_54278 | chr1:154390562-154394244 | Spleen | SE_54618 | chr1:154390203-154397361 | Stomach_Smooth_Muscle | SE_59139 | chr1:154375857-154394038 | Ly3 | SE_62668 | chr1:154357227-154415486 | Tonsil | SE_64458 | chr1:154390429-154393143 | NHEK | SE_65390 | chr1:154388596-154390466 | Pancreatic_islets | SE_65390 | chr1:154390491-154396964 | Pancreatic_islets | SE_67236 | chr1:154384840-154394484 | MM1S |
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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: 2 | ID | Chromosome | Start | End |
GH01I154416 | chr1 | 154388767 | 154390150 | GH01I154417 | chr1 | 154390221 | 154396888 |
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Enhancer Sequence | CTGCAAACTC CATCTCCGGG GTTCAAGTGA TTCTCCTACC TCAGCCTCCC GAGTAGCTGG 60 GATTACAGGC ATGCACCACT ATGCCCAGCT AATTTTTTTT TTTTTTTTTT TTTGAGATGG 120 AGTTTCACTC TTGTTGCCCA GGCTGGAGTG CAGTGGCATG ATCTCAGCTC ACTGCAACCT 180 TCCGGTTTCA AGCGATTCTC CTGCCTCAGC CTCCCAAGTA GCTGGGATTA CAGGCACCCG 240 CCACCATACC CGGCTAATTT TTGTATTTTT AGTAGAGACA GGATTTCACC ATGTTGGCCA 300 AGCTGATCTC AAACTCCTGA CCTTGTGATC CGACCTTCTC TGTCTCCCAA AGTGCTGGGA 360 TTACAGGCGT GAGCCACTTC ACCCGGCCTA ATTTTTGTAT TTTTTGGTAT GGATGGGGTT 420 TCACCATTTT GGCTAGGCTG GTCTTGAACT CCTGATCTCA GGTGATCCGC CAGCCTCAGC 480 CTCCCAAAGT GCTGAGATTA CAGGCGTGAG CTGCCGCACA TGGCCTTAGA TATCTTTTCC 540 TCTAATTAGT TTATAATCTC TGAGAGTTGA CCCAGGTTGT ACCTTCTTGG ACTGGAGCCA 600 GGTGGTTATC TCTGATGCTG CCAGAGGAGG ATTAGATGTT TTATCTCCTG AGTTGGTCAC 660 ACGCGCACGT GGGTCTCTGA GTCAGCATTG AGCATTACCT GTTTATGGGT CCAAAGGAGC 720 CTCCCTCCCA GACCCTCTCT CCAGCAGTGT ACAGTCCATC GTGTGGATGG GAGGAAGGCA 780 AGGCCAAGGT AAATACTGAC TCAGACAAAT ACAAGCAGGT ACAAGAAGTA CAAATACATA 840 TGTGGGGGAG GAGGGAGCAG GGGCCTGCCA GCCAAAGCTA GTCATCTGAG AAGAGGGGGT 900 TGCGGACAGG TGGGGCTGGG AGCTGAGTCA GAGAAGGTTG CTGGGCCTCC CATTAGAGCC 960 TGGGAGCCTT GACTTGCCGT AGCCTGCGGC CTTGCCTCTT CCTGGACAGT GGCCGAGGGT 1020 GCCCTCTGAA ATGTTAAGGA GAAATGAATG GGCCCAGATG GTGGGGTGAC TTGGGGAGGA 1080 CGCGAGATTT GGAGTCCAAG GGGAGGCAGT TTTAGGCTCT AACTCATCCT ATACACGCTG 1140 CGGCTGTGGG GGAAGGGAGA GAAAGGCCAA GGGCACGACT CCTGGCTCCT GAGAGTCCCC 1200 AGTGCCCCAT TAGGTTGGCA GCTGCAGTGA TGGCGCTGAC CCCCCCTTGT GCACACCCCT 1260 CAAGCCTCAG CATTCCCTTC CCTGGGCCTC TGAAGGGTGG AAAGATGTGA GAAGAGCAGG 1320 GAAGAGGAGA GGAAATTGGG AGAGGGGGAG AGAGAGGGTG GTGGGGAGCC CAGAGAAGGG 1380 AGCTGGGGGT GGAGCATGGA GAGGTACCTG GGCCAAGTAG AGAGAGGCTT TGGCCAGGCT 1440 CATCTGGGTC CAGCGTGGAT TCCCTCATGC ATGAGCTGTG TGAATTTGGG CAAGTTCCCT 1500 AACTTCTCTG ATCTCTTGTT GCCTCAACAA TGAAATGGGG ACAAGACTTC 1550
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