Tag | Content |
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EnhancerAtlas ID | HS116-28330 |
Organism | Homo sapiens |
Tissue/cell | Left_ventricle |
Coordinate | chr5:150438020-150439870 |
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: 4 | Chromosome | Start | End |
chr5 | 150438663 | 150438839 | chr5 | 150438616 | 150439117 | chr5 | 150438023 | 150438180 | chr5 | 150438255 | 150439122 |
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| Number: 1 | ID | Chromosome | Start | End |
GH05I151058 | chr5 | 150437946 | 150440970 |
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Enhancer Sequence | TGTTACCCTA CTGCAGACGG CACTGGGCCC AGCTCCCCTG CTGGGCATCT AAGGCCCTAC 60 AGCCGCAGGT CCCATCCACA GCAGCATCCA GTTGGGCTCC CCACTTTACC CTGCCTGAAC 120 CCACACACAC CAGGTCTGGT GTCTCTGCAT GTGTCCTCTC TGTGTCCTCT CTGCCTCTGC 180 AAGTTCTGCT CATCCTTCCC ACCCTGTCCA CGGCTCAGCT CCTCCAGCAG CCTCCCGGAA 240 ACAGTTATGG GAATCACAGG ACAGCAGAGC TACAGGGAGC CTCAGAGATC AGGCCGGGAA 300 ACCAAGCTAT GGGGAGGAGG AACTTGCCCA AAGTTGCCCT GTAAGTCAGT GGCAGAGGTA 360 TAACGAGAAC TGAGGTTTCC TGACTCGCCA TCCAGTGCTC TGCTGCACTG ACCTCCCACT 420 TCTCTGAACT CTGGAGGAAT GGCAATGACT ATAACCCCAA CTTGGCATTC CCTGAACACC 480 TGTGTAATGG CGTCAGTGTG CCGCATTCTA ACAAGAGGAA ATGCTGCTGT TTCAACTCTG 540 CATCCATTCC CCCACTGCCT CTTTCCACAA AGGAGCTGAG GTGGCAGATG CTGCTCTATT 600 TAAGGCTCAT GCGATGCTTC CCATGCCTGC GACTTCTCCA GACTACAAGC TTCAGAGCAC 660 AGGGAGGCTG TGTTGTCTTG GCTCAAGTGG CTCAGCAGAG ACAGGCACAC TGTAGAGCTA 720 ATGAGGAACT TACTACGTCA GTTAAAGTTA TCGGTCCAAA GTCAGAGTGA AACACTTTCT 780 GAGCAGGGGA TCTTGCCTCC ATGGCCAGCA TCTCAGAGCC CTCAGGGACA GAACAGGACA 840 AGGGGACAGA AGGTTCCAGG CGACAGAACA TAAAGAGCCT TTCCAATACT CAGAGCTGCC 900 TGAGGCAGTG GTGAGCCTCT CAACACTGAA GGCATGCTAG TTAGCCAGAC AGCCACCTGA 960 GGGGGCCCTG CACTGGGCAC TGACAGGTAC ATGGGGCAAC CAGTGAACAC AAGCATATTT 1020 GTCAGCCAAA CCTTTGTGAA GGGAGGCAGC AGGGATCAAT ATATCAGTGA AGGGCTAGAG 1080 CACCTATTGC TCGCATAACA ACAATTAAAG AAAAAAACTT AAAAGTGGGA AGGAAGGGAG 1140 AATGGAGAAG GTAGAAATTT AAGTCGTTTA AAGAATCTTC CAGACTTTTC ACAATGGTTC 1200 TTCAATAAGT CTGCCATTTT AAGAAAGAAC AGAAGGAGAT ATAGTTAGGA AAAAGGCAGC 1260 CAGTGTTGTA AGGTGTGGAA TGAGGATGCT GGGCAGACGC TCCAGAGCTG TACGAGAGAC 1320 AGAGAGAGAG AGAGAGAGAG AGAGAGAGAG AGAGAGAGAG AGAGAGAGAG TGTGTGTGTG 1380 TGTGTGTGTG TGTGTGTGTG TGTGTGTGCG CGCGCGCGCG CGCATGCGTG TAAGTGGAAA 1440 GTTGAACCTC CTTCCTGTGT GCTCCAAGAG TCTGCACAAA GAGCAAATCA CCTGTCTTAC 1500 AGGGCCCTGG GCCTTCCTGA CCCTTCTTTC TCCCCCGGGG TTGGAAGCCC ACAGACCCAA 1560 AGGGCTGAGT CATAGTGTGC GGAGGTGCCT GGCCCCTGGC AGAAGGCAAC AGGGCTGGCA 1620 AAGAGCCCAG GCTTTCACAA CGGTCGGGTG CCCGTGTGCT CCAAGTCGGG GAAGTCACTA 1680 GCCCAGGAAT TTGCATATGT GAGCGAGAAG CACCCTTTGC TCCTGCCCCT CGTGTATCCC 1740 CAAGTGACTC CAGGGTACCT AAGGGATCTG AACAGGTTCT GTGCCTCTCA CATGGTAGCA 1800 AGTGACAGGA CACAAAGAGG GCAGCAGGTC AAGCCCGGGG TCCTGCCCGT 1850
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