Tag | Content |
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EnhancerAtlas ID | HS089-06685 |
Organism | Homo sapiens |
Tissue/cell | Hela |
Coordinate | chr19:18588670-18590110 |
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) |
KLF4 | MA0039.3 | chr19:18588962-18588973 | CCACACCCTCT | + | 6.02 |
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| Number of super-enhancer constituents: 29 | ID | Coordinate | Tissue/cell |
SE_01013 | chr19:18588643-18590394 | Adrenal_Gland | SE_04099 | chr19:18588738-18590106 | Brain_Anterior_Caudate | SE_06012 | chr19:18587569-18592062 | Brain_Hippocampus_Middle | SE_09318 | chr19:18587289-18593113 | CD14 | SE_12155 | chr19:18588799-18590417 | CD3 | SE_15037 | chr19:18584199-18588821 | CD4_Memory_Primary_7pool | SE_15037 | chr19:18589123-18590617 | CD4_Memory_Primary_7pool | SE_17983 | chr19:18583928-18591813 | CD4p_CD25-_CD45ROp_Memory | SE_19379 | chr19:18587487-18590403 | CD4p_CD25-_Il17p_PMAstim_Th17 | SE_20439 | chr19:18584612-18591598 | CD56 | SE_21047 | chr19:18588603-18591663 | CD8_Memory_7pool | SE_22689 | chr19:18583973-18591671 | CD8_primiary | SE_23893 | chr19:18589312-18590189 | Colon_Crypt_2 | SE_26168 | chr19:18588425-18592741 | Duodenum_Smooth_Muscle | SE_26932 | chr19:18588122-18592042 | Esophagus | SE_31681 | chr19:18588601-18590332 | Gastric | SE_41123 | chr19:18587807-18590387 | Left_Ventricle | SE_41560 | chr19:18589244-18590155 | LNCaP | SE_42344 | chr19:18587292-18590373 | Lung | SE_44495 | chr19:18587274-18592340 | NHDF-Ad | SE_46271 | chr19:18587413-18593123 | Osteoblasts | SE_47511 | chr19:18588888-18589813 | Pancreas | SE_47511 | chr19:18589872-18590274 | Pancreas | SE_48120 | chr19:18587362-18592202 | Psoas_Muscle | SE_48694 | chr19:18588545-18590349 | Right_Atrium | SE_50125 | chr19:18585873-18593035 | Sigmoid_Colon | SE_51145 | chr19:18587336-18592595 | Skeletal_Muscle | SE_52434 | chr19:18585882-18592848 | Small_Intestine | SE_53541 | chr19:18587934-18592552 | Spleen |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr19 | 18589714 | 18590055 | chr19 | 18589200 | 18589384 |
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| Number: 1 | ID | Chromosome | Start | End |
GH19I018472 | chr19 | 18583787 | 18592442 |
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Enhancer Sequence | GATGTTTCTG CAAAAGATCA TTCAAGGCAT AAATTACGGT AGTGAGGCTG GGGTTTTGAA 60 TGTGGGGTGC TAAATAGATG GTGATGAGAA CACAAGGACT GGGTGGGGGG GATGAGAAAA 120 AACACAGAAA GCAGCTGGGG TGCAGTGCCC TGACAAGCCA ATCAAGGGCC CAGGAGGTGA 180 GTGTCGGCTG CAGACAGGCA GAGCCAGCTA GGTCCCTTCA CGGTGGGACC AGCTGTCACC 240 CTCTGTGCTC ACCAGCCTGG CCTGGTGGGG ACGCCTGACA GCATGTGGCC CACCACACCC 300 TCTTCTGGCT GCTCCCTCCA GAGCCAACAT GCGTGGTGTC ATGGCCGAAC CCTTGTCAGG 360 GGGGCCAAGC GCCTCGTTAC CTCATCTATG AAGCAGGACA GAGGGTCAGG AACAGACTGT 420 AGCACAGGTG ATTTCCCTGC TGCCTTAGAA GCTTTGGGGT TGGCCTCAGG CTGCATTAAT 480 TAAATAACGG GGTAACTCAG TAGCACATGA CACCTGCAGG GTACTGCCCA TCTCACACCC 540 AAGAACACCC AGCAGGGGAG AGCCATGCCT CAGGCCACCG CCTGCCCAGT CTCTGTAGAC 600 CCTCTGAGGG GTCATCACCC CCACAAGTCC TCTCAGGCCC TCGAGTGGCA AAAATCCAAC 660 TTTCATTACC CAGCATGAGG TATGGAACTG GGAGCTCCTG AGATACAAAG TCACCCCCGC 720 TGCTGTACTT CAGGCCAGGG CCCCAGGTGG GAGCTGGGGA GCCTGGTAGG GCCGCCACAG 780 CTGGCCTGAC ACAGTCAGCA GGTCAGCTGG GTCTTCAAGG CCGGACAGGC AGGCACTGAG 840 CTGTGCCGAG GCTGGTGCTC CCCAGACCCA ACTGGACTTC AGACCCTGAC TCGGAGAACA 900 GACCTCAACA CAGCAGGGCA GTGATGCCTG CGCCCTGCGG TCACTTGGCC TGGGCGCCCA 960 CTGGGGCTAC TGAACACAGA CTGGGAGACT CCTGTAGGCA GCTCCCCCTC AATGAGGACA 1020 CTCCTGTAAA GACAGCAATG CCTTTGGGAA AAGGGTCGAG GGTGCAGAGC CTGGGAGGCA 1080 GTGAGAGTCC TCAATGCTGA GACAGAGGAA AGGGTGAGGA GGAACCTCTC CAGGGCCAGA 1140 ATCCCCTGAT CCTCTCCCCT CCGGCAAAGA GCACTTCCGG GGATGAAGCA ACAGGAAGTG 1200 GCTTACGAAA TCCACCTCCA GGCCGAGTGA CCAGTTTACA GGAAGTGTGG TGGGTGAATC 1260 TTCCCCAGGG CACGAGGCAA TGTCTGGAGC CATTTCTGGT CCTCACCACT GAGGGCGGGG 1320 ACAGTCCCCA CCATCTGGCT CGGGGGAGGC CAGGGATGCT GCTCAGCACA CTGCAGGCAA 1380 CACAGAACCT CCTGCCCCAA ATGTCAAGCA GTGCAGGGGC TGAGAAGCCC TGGGCTGACC 1440
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