Tag | Content |
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EnhancerAtlas ID | HS065-04174 |
Organism | Homo sapiens |
Tissue/cell | GM18508 |
Coordinate | chr5:131796090-131797440 |
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) |
EWSR1-FLI1 | MA0149.1 | chr5:131796318-131796336 | GCTTCCTGCCATCCTGCC | - | 6.14 | EWSR1-FLI1 | MA0149.1 | chr5:131796322-131796340 | CCTGCCATCCTGCCTTCC | - | 6.76 | POU2F2 | MA0507.1 | chr5:131797204-131797217 | AAATGCAAATGAA | - | 6.59 |
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| Number of super-enhancer constituents: 32 | ID | Coordinate | Tissue/cell |
SE_00037 | chr5:131790656-131796338 | Adipose_Nuclei | SE_09163 | chr5:131788117-131797621 | CD14 | SE_10915 | chr5:131787711-131797453 | CD20 | SE_11856 | chr5:131788689-131797117 | CD3 | SE_13479 | chr5:131790641-131796411 | CD34_Primary_RO01536 | SE_14495 | chr5:131789106-131797177 | CD4_Memory_Primary_7pool | SE_17764 | chr5:131787920-131797394 | CD4p_CD25-_CD45ROp_Memory | SE_18258 | chr5:131787905-131797327 | CD4p_CD25-_Il17-_PMAstim_Th | SE_19103 | chr5:131790791-131797009 | CD4p_CD25-_Il17p_PMAstim_Th17 | SE_19972 | chr5:131788439-131797324 | CD56 | SE_20775 | chr5:131790546-131796689 | CD8_Memory_7pool | SE_22284 | chr5:131788012-131797561 | CD8_primiary | SE_23079 | chr5:131794575-131796517 | Colon_Crypt_1 | SE_23750 | chr5:131796561-131796935 | Colon_Crypt_2 | SE_25340 | chr5:131788298-131808279 | DND41 | SE_25784 | chr5:131790957-131797727 | Duodenum_Smooth_Muscle | SE_27629 | chr5:131790763-131801421 | Fetal_Intestine | SE_28559 | chr5:131794264-131804122 | Fetal_Intestine_Large | SE_30917 | chr5:131790670-131796844 | Fetal_Thymus | SE_31393 | chr5:131794548-131796995 | Gastric | SE_37771 | chr5:131791257-131796632 | HSMMtube | SE_39368 | chr5:131791092-131797698 | Jurkat | SE_40726 | chr5:131794433-131796690 | Left_Ventricle | SE_42103 | chr5:131794463-131796999 | Lung | SE_50023 | chr5:131791250-131797789 | RPMI-8402 | SE_50051 | chr5:131790768-131797132 | Sigmoid_Colon | SE_52336 | chr5:131790812-131797015 | Small_Intestine | SE_53285 | chr5:131790524-131796944 | Spleen | SE_55171 | chr5:131794927-131796428 | Thymus | SE_61818 | chr5:131790756-131837647 | Toledo | SE_62219 | chr5:131721125-131837948 | Tonsil | SE_66244 | chr5:131791092-131797698 | Jurkat |
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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 |
GH05I132452 | chr5 | 131788089 | 131817782 |
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Enhancer Sequence | GCTTCCCATT CTTACCAGCA GTTGGTATCT TCTGTCTTTT TCACACTGGC CATCTGAGTC 60 TCATAAGGAG ACTCCTCTCC TTCCACTGAG CCTGCATCCC AGCCTCTCCC CTTTCTTCAG 120 GGACCTCTCC CCAGCAATTA CGCCCTTCCA TTCTCTCAAC CAGGGAATCT TCAAACTCTT 180 CTTCTCCACT GGCTCCTGCT GTGCTCCTGT CTCCATCACC TGTATAATGC TTCCTGCCAT 240 CCTGCCTTCC CCGTGGAGTA CAGCCATGCT GTCTGCTGCT TACAGCCAAG ATTCTGGAAA 300 GAAATGTCTC CTTTTTCCTC GTCATCAACC ACTCATTTAT TCAGCAAGTG TTTCTTTTAC 360 ACTTGCCTGT GCTGGGCATG GCAGCAATGC AGCAGTGAAC AAAACCATCA GCCCTGCTCT 420 CATGCAGCTT ATAATCAAGT AGAGAGACAG ACATAAATGA TTAATAGATG CTCCTGTAAT 480 GGTGGTTGTG AGGTGTGCTG CCACAGCCCA GCCACACACG CCAGTTCCCT TCTCTGCACA 540 TGTACATGTC TGCTCATCCT TCCCACCTGA ACTCATGTGC CACCTCACTT ATGCCCCTTC 600 CCAATGCCGC ACCCACACAA CAGGGTGTCC CTCTGTGCCC ACAGCAGCCC TTGGGTATAA 660 CTGTTCCCCA CAGAGGCTGA ACCCCAAGGG CAGAGTCCAG GCCACACTCA CCACGGAGAC 720 CCCTGCCTGG CACAGAGCCC AGCCCAGCAG AGATGCTCAG AAGATGAATG AAAGTCCCTG 780 CTGAGATTGA TCCAATCTGT TTGTGAACAT CTCTGGGGTC CAAGAATTCA CGGCTTTCTT 840 TTTCTTTAGA GAGCCTTTTG TTTCTTTTTG CCATTATATA CTATATTTGG GTTAGGGCAC 900 AACAATGTGA ATATACTTAA TACTGAACTC TACACTTGAA AATGGTTAAG ATGGTAAAGT 960 TTTAAGTTAT ATGTATTTTG CCACAATTTT TTAAAATGCA GAGCATAGGT ACAAAGAAGG 1020 AAAAAAAGGG GGCAAGGTCC ATTTTATTGA GAAATAAAGA ACAAAGGGTT CAATTCAGAG 1080 AGGATTGGAT TTTAAAACGT AATTTAGATT AGGGAAATGC AAATGAAAAC CATAATAAGT 1140 AAGATACCAC TTCACATCTG TTAGGATGGC TATTTTAAAA CAACAAAAAC AACCTGAAAA 1200 TAAGTGTTGG CAAGGATGTG AAGAAATAGA TACCCTTGTG CATTGCTATT GGGAACGTAA 1260 AATCATGCAG CCTTTGTTGA AAACAATGTG GTGGTTCCTC AAAAACTTAG TTATCATATG 1320 ATCCCGCAGT TCCACTTCTA GGAATATACC 1350
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