Tag | Content |
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EnhancerAtlas ID | HS105-65564 |
Organism | Homo sapiens |
Tissue/cell | IMR90 |
Coordinate | chr5:131796240-131797810 |
SNPs | Number: 2 | 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 | ZNF263 | MA0528.1 | chr5:131797778-131797799 | GAAGGAGGAAGAACAGGGAGA | + | 7.89 |
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| Number of super-enhancer constituents: 31 | ID | Coordinate | Tissue/cell |
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: 2 | Chromosome | Start | End |
chr5 | 131796798 | 131796851 | chr5 | 131797501 | 131797604 |
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| Number: 1 | ID | Chromosome | Start | End |
GH05I132452 | chr5 | 131788089 | 131817782 |
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Enhancer Sequence | TTCTCTCAAC CAGGGAATCT TCAAACTCTT CTTCTCCACT GGCTCCTGCT GTGCTCCTGT 60 CTCCATCACC TGTATAATGC TTCCTGCCAT CCTGCCTTCC CCGTGGAGTA CAGCCATGCT 120 GTCTGCTGCT TACAGCCAAG ATTCTGGAAA GAAATGTCTC CTTTTTCCTC GTCATCAACC 180 ACTCATTTAT TCAGCAAGTG TTTCTTTTAC ACTTGCCTGT GCTGGGCATG GCAGCAATGC 240 AGCAGTGAAC AAAACCATCA GCCCTGCTCT CATGCAGCTT ATAATCAAGT AGAGAGACAG 300 ACATAAATGA TTAATAGATG CTCCTGTAAT GGTGGTTGTG AGGTGTGCTG CCACAGCCCA 360 GCCACACACG CCAGTTCCCT TCTCTGCACA TGTACATGTC TGCTCATCCT TCCCACCTGA 420 ACTCATGTGC CACCTCACTT ATGCCCCTTC CCAATGCCGC ACCCACACAA CAGGGTGTCC 480 CTCTGTGCCC ACAGCAGCCC TTGGGTATAA CTGTTCCCCA CAGAGGCTGA ACCCCAAGGG 540 CAGAGTCCAG GCCACACTCA CCACGGAGAC CCCTGCCTGG CACAGAGCCC AGCCCAGCAG 600 AGATGCTCAG AAGATGAATG AAAGTCCCTG CTGAGATTGA TCCAATCTGT TTGTGAACAT 660 CTCTGGGGTC CAAGAATTCA CGGCTTTCTT TTTCTTTAGA GAGCCTTTTG TTTCTTTTTG 720 CCATTATATA CTATATTTGG GTTAGGGCAC AACAATGTGA ATATACTTAA TACTGAACTC 780 TACACTTGAA AATGGTTAAG ATGGTAAAGT TTTAAGTTAT ATGTATTTTG CCACAATTTT 840 TTAAAATGCA GAGCATAGGT ACAAAGAAGG AAAAAAAGGG GGCAAGGTCC ATTTTATTGA 900 GAAATAAAGA ACAAAGGGTT CAATTCAGAG AGGATTGGAT TTTAAAACGT AATTTAGATT 960 AGGGAAATGC AAATGAAAAC CATAATAAGT AAGATACCAC TTCACATCTG TTAGGATGGC 1020 TATTTTAAAA CAACAAAAAC AACCTGAAAA TAAGTGTTGG CAAGGATGTG AAGAAATAGA 1080 TACCCTTGTG CATTGCTATT GGGAACGTAA AATCATGCAG CCTTTGTTGA AAACAATGTG 1140 GTGGTTCCTC AAAAACTTAG TTATCATATG ATCCCGCAGT TCCACTTCTA GGAATATACC 1200 CAAAAGAATT GAAAGCAGGG ACTCAAAGTG ATATTTGTAC ACCAGTGTTT GTAGCAGTAT 1260 TATTCACAAT AGCCAAAAGG TGGAAACAAC CCAGATGTCC ATGACAAGAG GAGTGGATAA 1320 ACAAAATATG GTGAATATGT ACAATGGAAC ATAATTCAGC TTTAAAAAGG AATGAAATTC 1380 TGGTACATGT TATAACATAG ATGAACCTTA AAAACATTAT GCTAAGTGAA ATAAGCCAGA 1440 CACAGAAGGA AAAATACCAG ATGATCCCAC TTATATGAGG TACCTAGAAT AGTGAAATTC 1500 ATAGAGACAG AAAGTAGAAG GATGGTTGCC AGGGGCTGGA AGGAGGAAGA ACAGGGAGAT 1560 ACTGCTTAGT 1570
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