Tag | Content |
---|
EnhancerAtlas ID | HS193-28900 |
Organism | Homo sapiens |
Tissue/cell | U87 |
Coordinate | chr5:150455080-150456920 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
SP2 | MA0516.2 | chr5:150456429-150456446 | CAAAGCCCCACCCACAT | + | 6.07 |
|
| Number of super-enhancer constituents: 35 | ID | Coordinate | Tissue/cell |
SE_01392 | chr5:150455183-150456483 | Adrenal_Gland | SE_02605 | chr5:150454842-150456793 | Astrocytes | SE_09226 | chr5:150454881-150456345 | CD14 | SE_15204 | chr5:150455351-150456738 | CD4_Memory_Primary_7pool | SE_17941 | chr5:150455174-150468518 | CD4p_CD25-_CD45ROp_Memory | SE_18317 | chr5:150453499-150468432 | CD4p_CD25-_Il17-_PMAstim_Th | SE_19111 | chr5:150454771-150468362 | CD4p_CD25-_Il17p_PMAstim_Th17 | SE_23141 | chr5:150454841-150456487 | Colon_Crypt_1 | SE_23836 | chr5:150455200-150456402 | Colon_Crypt_2 | SE_25002 | chr5:150455220-150456142 | Colon_Crypt_3 | SE_27123 | chr5:150453721-150456784 | Esophagus | SE_28253 | chr5:150455196-150456191 | Fetal_Intestine | SE_31853 | chr5:150454852-150456622 | Gastric | SE_32472 | chr5:150455256-150456379 | GM12878 | SE_35096 | chr5:150455032-150456331 | HeLa | SE_36009 | chr5:150453747-150457034 | HMEC | SE_37013 | chr5:150454502-150457000 | HSMMtube | SE_40909 | chr5:150454783-150457437 | Left_Ventricle | SE_42116 | chr5:150454765-150456478 | Lung | SE_47695 | chr5:150455440-150456016 | Pancreas | SE_48796 | chr5:150455153-150456074 | Right_Atrium | SE_50074 | chr5:150454947-150456817 | Sigmoid_Colon | SE_51316 | chr5:150455114-150456779 | Skeletal_Muscle | SE_51803 | chr5:150454642-150456818 | Skeletal_Muscle_Myoblast | SE_52353 | chr5:150454959-150456784 | Small_Intestine | SE_53309 | chr5:150455146-150456609 | Spleen | SE_56023 | chr5:150454657-150457156 | u87 | 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_63588 | chr5:150454628-150456818 | HSMM | SE_64498 | chr5:150454519-150456918 | NHEK | SE_67545 | chr5:150454657-150457156 | u87 |
|
| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr5 | 150455274 | 150456118 | chr5 | 150455260 | 150455927 |
|
Enhancer Sequence | CTACTGTTGC CATCTTTATG TCCATGAGGA CCTGATATTT AGCTCCACTT ATAAGTGAGA 60 AAATGCAGCA TTTGGTTTTC TGTTCCTGTG TTAATGTGCT TAGGACAATA TTTTCTAAAA 120 GTCTATGTTG CCAGTTTCCT GAGGACCAGA TCACGCAGGA GTTGCACCTG CAGAGACAGA 180 AGTGGGCTGG AGAGGGACCA GGGCTCCTAA GTCTGCTGCT GAAGCTGACT ATAGCGAAGG 240 CAAAGGACAA GTGGCCTGAA GGCCAACAGA GAGCCTGGCC AATGCTCTGC CCAGTGGGTG 300 GAGACTGAGC CAAAGGCCCT TGACTCATAG GGCAGTCCCA TACCTGCCCT GGCCTCTCAG 360 CATGACTCCT TGGTGACACA ACTCCCACAG CACCCACACA CCTACACCCA CCTACCCCAC 420 ACACACACCC CTGCCTGGGC TGCCCGGTTT GTCCACTGTG TAGGTGCTCA AGGACGCAGA 480 GCTCCTGCCT CTCAAGGAAC AGCCTCAGGG TGAGGTCCCT GGGAGAGAAG AGTTCAGCTC 540 TGCCCAGAGC AGCCCTCAGA CAAACAGCCA GCTGCTGCTC ACCAGTCATC CATTCCAATC 600 TGAAGAGTGA CTGTCCTGGG CCAGTCATGG GAAAATCATC AAGAACTTCC CACAATGGTC 660 ATGGTGGCCG CCAAGGTCTT TCTCTGGGGG TTGGGAGCTG TGCTCCCCCA CAAAACAAGG 720 GGACCCAGCT GCCCTGTGCC TTCCTGTGGC AACTCTCTGG AGGATGCCTG GATACCCTCC 780 CTACAGACGG CCAGGGATAG GAGGGGCAGG CACTGCAGGC ATGTGGGGGC ATAGCAGCAA 840 GAATCTAGGA GGGCAGGCAC AGCAAGGCCT GGCCCAGAGG GAAACCAGGA GCTGCCAGAG 900 CCAAAGAGAG GGTGACCCAA TCATTGGTTG TTATAGAGTT TTTAAGACTT GGAAGAGAAT 960 GCCCTGAGAT GCCAGAGAGT GAAACATTTT CATTCTAAAG CTGGGAAACC AAAGTCGGCA 1020 AAGGCGAACA GACGTGCCCA CAGCCACATG GGACAGCAGT GGCACAGAAG AAATGCACAC 1080 CTCGTCCTCT GGTGGCCACT GTGCACTCTC TTACCACACC ATGCTACTGC TCAACCTCTC 1140 CCCCTCCCTC ACAGTGGTCA GGTAAGCAAT GAGGGAAAAT GATGGAGGTG AGAAAGGAAG 1200 AACCCGGGCT GATGTGGGCC CACAAAAGAA AGAAGTCTGG AATAACACTG GAAGGGGCTG 1260 CCTACGAGGT GGAAAGCGCC CTGATCCCAG GGGTCGGGGT CACGCAGAGG GGCACTGGGG 1320 CTGTTGAGGG AATGCAAGCC AGGTGTCTTC AAAGCCCCAC CCACATCTGA GTTTCCGCCA 1380 CTCCAAACAG GGACAGATGT TTGAGACAAA GCAAAGGACA ACTCATCCAG AGGGGACACA 1440 GCATGGACCA CAAGTGGCAG AGGGTTGAAG GCAAGTGTCT TAGTCTGCTT TCTGCAACTA 1500 TTCTGTTGAA TATCACAGAC TGGGTAATTT ATAAAGAACA AGTTTATTTG GCTCATGGTT 1560 CTGGATGATG AGAAATCCAA GTGCATGACA CCACCATCTG ACAAGGGTCA TGCCAAGGTG 1620 GAAGACAGAA GGAGAAAATG AGTGATTGAA ATAGAGAGTG TATTAGCCAA ACTGGCCCCT 1680 TTTATAACTA ACCTCCCGTC CCCCTACCCC GTGATAGTGA CATTAATCTA TTTATGAGGG 1740 CAGAGCTGAC AATCCATTCA TGAAGCAGAG GGATTACGTT TCCAAGATAT GAACTTTTGG 1800 GGGACACATT CAAACCTTAG CAGCAAGTTA TCCAGAGCAC 1840
|