Tag | Content |
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EnhancerAtlas ID | HS173-01337 |
Organism | Homo sapiens |
Tissue/cell | SH-SY5Y |
Coordinate | chr1:223900580-223902290 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
PRDM1 | MA0508.2 | chr1:223902182-223902192 | GTGAAAGTGA | - | 6.02 | ZNF263 | MA0528.1 | chr1:223900924-223900945 | GGAGCTGGAAGGGAAGGGGAA | + | 6.37 |
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| Number of super-enhancer constituents: 38 | ID | Coordinate | Tissue/cell |
SE_00224 | chr1:223891886-223912166 | Adipose_Nuclei | SE_01908 | chr1:223899434-223901751 | Aorta | SE_02306 | chr1:223899487-223903687 | Astrocytes | SE_04026 | chr1:223899460-223901964 | Brain_Anterior_Caudate | SE_05036 | chr1:223899387-223902276 | Brain_Cingulate_Gyrus | SE_05972 | chr1:223899184-223905867 | Brain_Hippocampus_Middle | SE_07996 | chr1:223899335-223902248 | Brain_Inferior_Temporal_Lobe | SE_09681 | chr1:223899395-223907924 | CD14 | SE_19702 | chr1:223899422-223907008 | CD4p_CD25-_Il17p_PMAstim_Th17 | SE_23408 | chr1:223899450-223902270 | Colon_Crypt_1 | SE_24051 | chr1:223899535-223901916 | Colon_Crypt_2 | SE_25230 | chr1:223899578-223902311 | Colon_Crypt_3 | SE_26209 | chr1:223899230-223905388 | Duodenum_Smooth_Muscle | SE_26925 | chr1:223899336-223904834 | Esophagus | SE_31491 | chr1:223898405-223906097 | Gastric | SE_33950 | chr1:223900271-223904290 | HCC1954 | SE_34545 | chr1:223899419-223904575 | HCT-116 | SE_34979 | chr1:223899218-223904777 | HeLa | SE_36294 | chr1:223899426-223904613 | HMEC | SE_37129 | chr1:223899390-223911201 | HSMMtube | SE_38254 | chr1:223899363-223904539 | HUVEC | SE_38957 | chr1:223899577-223902313 | IMR90 | SE_41495 | chr1:223899335-223902135 | Left_Ventricle | SE_42269 | chr1:223899365-223902112 | Lung | SE_44530 | chr1:223900206-223905349 | NHDF-Ad | SE_44904 | chr1:223899464-223902190 | NHLF | SE_45872 | chr1:223899383-223910101 | Osteoblasts | SE_49408 | chr1:223899479-223901876 | Right_Atrium | SE_50365 | chr1:223899342-223907084 | Sigmoid_Colon | SE_51879 | chr1:223899648-223902193 | Skeletal_Muscle_Myoblast | SE_53249 | chr1:223899545-223902028 | Small_Intestine | SE_55958 | chr1:223898795-223906601 | u87 | SE_58098 | chr1:223900170-223900759 | VACO_9m | SE_63671 | chr1:223899648-223902254 | HSMM | SE_64794 | chr1:223900231-223904926 | NHEK | SE_65644 | chr1:223899375-223901874 | Pancreatic_islets | SE_67677 | chr1:223898795-223906601 | u87 | SE_68376 | chr1:223892363-223922876 | TC32 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr1 | 223902180 | 223902241 | chr1 | 223901276 | 223901546 |
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Enhancer Sequence | TAGGAAGCGC GCGGCAGGAC GCGGGCAGGG CGGGGTGCCG GGCAGGGCGG GGTGCAGGCC 60 GGCCCGCGGC GCGCTGGGGC GGGGGGCAGC CCGGGTGCTG CAGTGGGGAA GCCGCAAGCC 120 AGGACCTCGC AGTCCTGCGA CACCTCCGCG CCGCCAGAGC CCGGGACTCT GTTCGAGCGT 180 GGGGGGACTC CCGGGGCCTT CCCTCTCTTC CACCCACCAC GCTTTCCTGG GCGGGTCGAG 240 GCGAATCACT GCCCTCAGAT CCCACTAGCA GGCCACTTTA GGACTTCACA AAAACTCAGG 300 GTGATGCAGG AGGCCGGGGT GAAACTTTGA TTGGACTCTA GCGGGGAGCT GGAAGGGAAG 360 GGGAATCGGG TCTGCAGGGA AGGGACGGTG AGAGGCAGCA TCTACCAGAC AAAGTCCGTC 420 TCCAACTGGG GTTCTGTCTG TTCATGGAGG GGGACAGGCC ATAGCCTGGT CATTTTGTGA 480 CTAAGGATAG TCTCCTGCAG CCCTGGGGTT AGATTTATTT TTCCAAAGGG GAGCCAGCGA 540 TACCTCCTCA TAACATTGAC ACTGGTAATT AACCCAGGAC ACGGAGGTGT CTCATGGTTT 600 CCCTGGCGGG AATCACCCGG GAAACCTCCG GGAGCCCTCC AGACCCCCTT ATCCCGTCCC 660 CCAGGGTCTC TGACCTCCCG GCCCTGGGAC AACTTGTGCT CCCCAATCTA CTTGTCCATT 720 CTGTTTCTTG GGGAACCCCT GAGGCTCCTC CTCCTTTGGG ACACTTCCCC AGGCTTCCCC 780 TACCACGCCT AGGAAAGCCT GCCCTGAAGT CCAACTTCTA GATTCCTGTT GTGAGAACAA 840 GGCTTCCAGC TCTGCTTCCA CACCCAGCAG CCTCCCAGGT CACCTTCTGT TACCCTAAAT 900 CCAGCCCATA GGTAGCAAGG GCTGCAGGAA GCGCCCTAGC CCAGACTCAG AGCACTTGGG 960 TTCTTCTTCT TGCTAACCTG CTGGTGACCT TGAACGAGCC ATTTAACCTC TCTGTGCCTC 1020 CATGTCTTCA TCTAAAAGAA AACATGCTGC CTAAATATTT TCTCTCTTTT GTGGCCCACT 1080 AGGCCCTGCC GTCATGGCCT CCTTTCAGTC TCTCAAAGAG CCGGTTCTTT CCTGCATGAG 1140 GCCTTCTCAC CAGCAAGGCA CGCTGTTACC TGGAGTGTGG CTCACTCTCA TTCTTCCCAA 1200 CTTAGTCACA TGTTCCCTTC CTAAAGAGGT CTTTTCTGAC CCTTCTTAGC AGCCACCTCC 1260 CCACCTTGTT TTTCTCTGTC ACCCCACTCA TTTCCTTCAT AGCATTGTCA CAGTTTAGAA 1320 TATAATCACA TGTATTTGTT CTTCCTACTG AACTGCAGGA ATCATGTGTA TATTATTTAC 1380 CAGTATATCC CCAGTGCCTG ACACATAACC ATGCCTTTCA CAGTATTCAT TCATTCATTC 1440 ATTCATTCAT TTACTCACTC ATTTGACAAC ACTGATTGAG CACCTGTTAC ATGCCAGGCA 1500 CTGTCCTGAG AGCTCAGGAG ATACACCAGT GAACACAAAA GAAGTGACTG TTTGTAGAAT 1560 ATGGATGCAG GATTGTAATG TGCCTCAAAT GAAATTATGG TTGTGAAAGT GATACGCTGA 1620 CCTGACTCAG TGCCTCACAC CTGTAATCCC AGCACTATGG GAGGCCAAGG TGGGAGGATC 1680 GCTTGAGCCA GGAGTTCAAG ACCAGCCTGG 1710
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