| Tag | Content |
|---|
EnhancerAtlas ID | HS193-15861 |
Organism | Homo sapiens |
Tissue/cell | U87 |
Coordinate | chr19:1856700-1857800 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| KLF5 | MA0599.1 | chr19:1857129-1857139 | GCCCCGCCCC | + | 6.02 | | SPIB | MA0081.2 | chr19:1856870-1856882 | CACTTCCCCTTT | - | 6.07 | | ZNF740 | MA0753.2 | chr19:1856952-1856965 | GTGGGGGGGGCGA | - | 7.04 |
|
| | Number of super-enhancer constituents: 29 | ID | Coordinate | Tissue/cell |
| SE_05653 | chr19:1854545-1857986 | Brain_Cingulate_Gyrus | | SE_12493 | chr19:1856733-1856887 | CD34_adult | | SE_12493 | chr19:1857265-1857408 | CD34_adult | | SE_12493 | chr19:1857439-1857553 | CD34_adult | | SE_15325 | chr19:1851179-1863643 | CD4_Memory_Primary_7pool | | SE_17066 | chr19:1855162-1858408 | CD4p_CD225int_CD127p_Tmem | | SE_18006 | chr19:1854567-1858438 | CD4p_CD25-_CD45ROp_Memory | | SE_20207 | chr19:1854775-1857036 | CD56 | | SE_20207 | chr19:1857073-1858104 | CD56 | | SE_20804 | chr19:1851994-1859364 | CD8_Memory_7pool | | SE_22514 | chr19:1854652-1858255 | CD8_primiary | | SE_23274 | chr19:1855536-1863748 | Colon_Crypt_1 | | SE_23831 | chr19:1855456-1863700 | Colon_Crypt_2 | | SE_24756 | chr19:1851482-1865735 | Colon_Crypt_3 | | SE_27152 | chr19:1853176-1865991 | Esophagus | | SE_34338 | chr19:1852133-1866086 | HCT-116 | | SE_41602 | chr19:1854125-1856964 | LNCaP | | SE_41602 | chr19:1857007-1862712 | LNCaP | | SE_45211 | chr19:1855501-1858228 | NHLF | | SE_50407 | chr19:1852750-1865843 | Sigmoid_Colon | | SE_52963 | chr19:1854521-1862878 | Small_Intestine | | SE_53592 | chr19:1853107-1866012 | Spleen | | SE_57652 | chr19:1857385-1857987 | VACO_503 | | SE_61842 | chr19:1851542-1865663 | Toledo | | SE_68584 | chr19:1847293-1885536 | TC71 | | SE_68585 | chr19:1847293-1885536 | TC71 | | SE_68586 | chr19:1847293-1885536 | TC71 | | SE_68587 | chr19:1847293-1885536 | TC71 | | SE_69023 | chr19:1852746-1858528 | H9 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | TGGGGACGGG GTCTGGCTGT GGGAGCGCGG CTGGAGCAGA CCACGGGATT GGGGCTCGCG 60
CCCCTCCAGG GAACATGCCG CCGTGTCGCC ATCTTGCAAG GCACAGGCGG GGAGGCGGCA 120
GGAGGGAAGG GGGAACATCC CACGGCTGGG TGCCGGACAG TCAGTTGGTT CACTTCCCCT 180
TTCAGGGCGG CGGGGCTGGT CTCCACTCCC TCTCCCCCAG TTCCACTTTG CAAGGAGGAG 240
CAGGTTGCCG GGGTGGGGGG GGCGACCGGG GCAGGGGCGC GCAGCCGCTG GGAACACAGC 300
TGCCGCACGT AGCTCGGCGG CGGCGGCGGG GACATCCGCA GCCCCAGCCG GCCCCGCTCA 360
CGTGGTCCCA CTCCCGCCGG GGCCAGGGGG CCCGGGCCAG GGTCGCCTCT CCGGCCTGGG 420
TGCCTGCCAG CCCCGCCCCG CGCTTGGAGA CTGAGGCGCG CACATGCGCA CGTGGGTGGC 480
GGGGCAGGGG GTGCACGGGC TACCCACCCA CGCTGCGCTG GGCGAAGCGC CTCTGCGAAA 540
TGCCAGGCCC TGCCTCGCAC ACAATCCACT CGCAGGGAGG AGGGTGGGGT GAACTTGTGG 600
GGGCCCAGAG CGCGCTGCTC CTAGCCAGCC GGGCCCCCAG GTGCACAGCC ACCCAGCTGC 660
TCCGCGCTAC CTGGCCGAGA CGCAGCGCCC TGAGGATGCG GTGGGTGGGG ACAACGCGGG 720
AGGGCAGTGT GGGCGGGGCC GCGGTGGACT TGACCCTCTG ACTCAGGCTG GGCCCGGGTG 780
AGCTCAGGAC AGCCTCGGAA ACAGGCAGGC TCAGAAAAAT GGAGTCCAGG AAGTCCTGGA 840
AACCTGGCCC GGCCCCGTCT GAGCCGGCAC AGGAGGGGCC TGGAGACAGG ACTGCGGGAC 900
TGTGCCAAGG GCCCTGGTTC CGACAGGGAA GCCTCACCTC CTGAGCTTGT CTGGGGGGCC 960
TTGGGGTGGG GAGGGGGGCT GTGGCCGGCT GCCTGCCGGG GCACTCACGT CCACCTAACA 1020
GGTGGGGTCG GGTCTGTAGG GGAGGGCACA GGTGGGGAAG ACCAGCCCCA GCCGCAAAGC 1080
AAGCATCCCA GGAGAGCCAG 1100
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