Tag | Content |
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EnhancerAtlas ID | HS165-12571 |
Organism | Homo sapiens |
Tissue/cell | Ramos |
Coordinate | chr5:150438190-150439870 |
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 | chr5:150439147-150439165 | GGAAGGAAGGGAGAATGG | + | 6.91 | TFAP2A | MA0003.3 | chr5:150438916-150438927 | TGCCTGAGGCA | - | 6.02 |
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| Number of super-enhancer constituents: 27 | ID | Coordinate | Tissue/cell |
SE_01392 | chr5:150439301-150440166 | Adrenal_Gland | SE_09226 | chr5:150430453-150448684 | CD14 | SE_13196 | chr5:150439481-150440266 | CD34_Primary_RO01480 | SE_13605 | chr5:150438251-150440561 | CD34_Primary_RO01536 | SE_17941 | chr5:150438094-150440560 | CD4p_CD25-_CD45ROp_Memory | SE_18317 | chr5:150437917-150440808 | CD4p_CD25-_Il17-_PMAstim_Th | SE_19111 | chr5:150438350-150440669 | CD4p_CD25-_Il17p_PMAstim_Th17 | SE_23836 | chr5:150439436-150440004 | Colon_Crypt_2 | SE_25989 | chr5:150437969-150440640 | Duodenum_Smooth_Muscle | SE_31853 | chr5:150439365-150440264 | Gastric | SE_32472 | chr5:150438135-150440857 | GM12878 | SE_37013 | chr5:150437792-150444781 | HSMMtube | SE_40909 | chr5:150437833-150445066 | Left_Ventricle | SE_42116 | chr5:150437801-150445050 | Lung | SE_47695 | chr5:150439446-150440015 | Pancreas | SE_48252 | chr5:150438156-150445152 | Psoas_Muscle | SE_48796 | chr5:150437870-150441468 | Right_Atrium | SE_50074 | chr5:150439258-150441029 | Sigmoid_Colon | SE_51316 | chr5:150437890-150450702 | Skeletal_Muscle | SE_52353 | chr5:150437881-150441035 | Small_Intestine | SE_53309 | chr5:150437704-150445004 | Spleen | SE_58791 | chr5:150431451-150475486 | Ly1 | SE_59083 | chr5:150437761-150478457 | Ly3 | SE_60748 | chr5:150431201-150478526 | DHL6 | SE_61344 | chr5:150438255-150475360 | HBL1 | SE_62297 | chr5:150437930-150538770 | Tonsil | SE_67545 | chr5:150439566-150440596 | u87 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 3 | Chromosome | Start | End |
chr5 | 150438663 | 150438839 | chr5 | 150438616 | 150439117 | chr5 | 150438255 | 150439122 |
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| Number: 1 | ID | Chromosome | Start | End |
GH05I151058 | chr5 | 150437946 | 150440970 |
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Enhancer Sequence | CTGCCTCTGC AAGTTCTGCT CATCCTTCCC ACCCTGTCCA CGGCTCAGCT CCTCCAGCAG 60 CCTCCCGGAA ACAGTTATGG GAATCACAGG ACAGCAGAGC TACAGGGAGC CTCAGAGATC 120 AGGCCGGGAA ACCAAGCTAT GGGGAGGAGG AACTTGCCCA AAGTTGCCCT GTAAGTCAGT 180 GGCAGAGGTA TAACGAGAAC TGAGGTTTCC TGACTCGCCA TCCAGTGCTC TGCTGCACTG 240 ACCTCCCACT TCTCTGAACT CTGGAGGAAT GGCAATGACT ATAACCCCAA CTTGGCATTC 300 CCTGAACACC TGTGTAATGG CGTCAGTGTG CCGCATTCTA ACAAGAGGAA ATGCTGCTGT 360 TTCAACTCTG CATCCATTCC CCCACTGCCT CTTTCCACAA AGGAGCTGAG GTGGCAGATG 420 CTGCTCTATT TAAGGCTCAT GCGATGCTTC CCATGCCTGC GACTTCTCCA GACTACAAGC 480 TTCAGAGCAC AGGGAGGCTG TGTTGTCTTG GCTCAAGTGG CTCAGCAGAG ACAGGCACAC 540 TGTAGAGCTA ATGAGGAACT TACTACGTCA GTTAAAGTTA TCGGTCCAAA GTCAGAGTGA 600 AACACTTTCT GAGCAGGGGA TCTTGCCTCC ATGGCCAGCA TCTCAGAGCC CTCAGGGACA 660 GAACAGGACA AGGGGACAGA AGGTTCCAGG CGACAGAACA TAAAGAGCCT TTCCAATACT 720 CAGAGCTGCC TGAGGCAGTG GTGAGCCTCT CAACACTGAA GGCATGCTAG TTAGCCAGAC 780 AGCCACCTGA GGGGGCCCTG CACTGGGCAC TGACAGGTAC ATGGGGCAAC CAGTGAACAC 840 AAGCATATTT GTCAGCCAAA CCTTTGTGAA GGGAGGCAGC AGGGATCAAT ATATCAGTGA 900 AGGGCTAGAG CACCTATTGC TCGCATAACA ACAATTAAAG AAAAAAACTT AAAAGTGGGA 960 AGGAAGGGAG AATGGAGAAG GTAGAAATTT AAGTCGTTTA AAGAATCTTC CAGACTTTTC 1020 ACAATGGTTC TTCAATAAGT CTGCCATTTT AAGAAAGAAC AGAAGGAGAT ATAGTTAGGA 1080 AAAAGGCAGC CAGTGTTGTA AGGTGTGGAA TGAGGATGCT GGGCAGACGC TCCAGAGCTG 1140 TACGAGAGAC AGAGAGAGAG AGAGAGAGAG AGAGAGAGAG AGAGAGAGAG AGAGAGAGAG 1200 TGTGTGTGTG TGTGTGTGTG TGTGTGTGTG TGTGTGTGCG CGCGCGCGCG CGCATGCGTG 1260 TAAGTGGAAA GTTGAACCTC CTTCCTGTGT GCTCCAAGAG TCTGCACAAA GAGCAAATCA 1320 CCTGTCTTAC AGGGCCCTGG GCCTTCCTGA CCCTTCTTTC TCCCCCGGGG TTGGAAGCCC 1380 ACAGACCCAA AGGGCTGAGT CATAGTGTGC GGAGGTGCCT GGCCCCTGGC AGAAGGCAAC 1440 AGGGCTGGCA AAGAGCCCAG GCTTTCACAA CGGTCGGGTG CCCGTGTGCT CCAAGTCGGG 1500 GAAGTCACTA GCCCAGGAAT TTGCATATGT GAGCGAGAAG CACCCTTTGC TCCTGCCCCT 1560 CGTGTATCCC CAAGTGACTC CAGGGTACCT AAGGGATCTG AACAGGTTCT GTGCCTCTCA 1620 CATGGTAGCA AGTGACAGGA CACAAAGAGG GCAGCAGGTC AAGCCCGGGG TCCTGCCCGT 1680
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