Tag | Content |
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EnhancerAtlas ID | HS037-17217 |
Organism | Homo sapiens |
Tissue/cell | ESC |
Coordinate | chr19:1856800-1858200 |
SNPs | Number: 2 | ID | Chromosome | Position | Genome Version |
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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 |
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| Number of super-enhancer constituents: 28 | ID | Coordinate | Tissue/cell |
SE_05653 | chr19:1854545-1857986 | Brain_Cingulate_Gyrus | SE_12493 | chr19:1857265-1857408 | CD34_adult | SE_12794 | chr19:1857805-1857967 | CD34_fetal | 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 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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Enhancer Sequence | GCACAGGCGG GGAGGCGGCA GGAGGGAAGG GGGAACATCC CACGGCTGGG TGCCGGACAG 60 TCAGTTGGTT CACTTCCCCT TTCAGGGCGG CGGGGCTGGT CTCCACTCCC TCTCCCCCAG 120 TTCCACTTTG CAAGGAGGAG CAGGTTGCCG GGGTGGGGGG GGCGACCGGG GCAGGGGCGC 180 GCAGCCGCTG GGAACACAGC TGCCGCACGT AGCTCGGCGG CGGCGGCGGG GACATCCGCA 240 GCCCCAGCCG GCCCCGCTCA CGTGGTCCCA CTCCCGCCGG GGCCAGGGGG CCCGGGCCAG 300 GGTCGCCTCT CCGGCCTGGG TGCCTGCCAG CCCCGCCCCG CGCTTGGAGA CTGAGGCGCG 360 CACATGCGCA CGTGGGTGGC GGGGCAGGGG GTGCACGGGC TACCCACCCA CGCTGCGCTG 420 GGCGAAGCGC CTCTGCGAAA TGCCAGGCCC TGCCTCGCAC ACAATCCACT CGCAGGGAGG 480 AGGGTGGGGT GAACTTGTGG GGGCCCAGAG CGCGCTGCTC CTAGCCAGCC GGGCCCCCAG 540 GTGCACAGCC ACCCAGCTGC TCCGCGCTAC CTGGCCGAGA CGCAGCGCCC TGAGGATGCG 600 GTGGGTGGGG ACAACGCGGG AGGGCAGTGT GGGCGGGGCC GCGGTGGACT TGACCCTCTG 660 ACTCAGGCTG GGCCCGGGTG AGCTCAGGAC AGCCTCGGAA ACAGGCAGGC TCAGAAAAAT 720 GGAGTCCAGG AAGTCCTGGA AACCTGGCCC GGCCCCGTCT GAGCCGGCAC AGGAGGGGCC 780 TGGAGACAGG ACTGCGGGAC TGTGCCAAGG GCCCTGGTTC CGACAGGGAA GCCTCACCTC 840 CTGAGCTTGT CTGGGGGGCC TTGGGGTGGG GAGGGGGGCT GTGGCCGGCT GCCTGCCGGG 900 GCACTCACGT CCACCTAACA GGTGGGGTCG GGTCTGTAGG GGAGGGCACA GGTGGGGAAG 960 ACCAGCCCCA GCCGCAAAGC AAGCATCCCA GGAGAGCCAG GAAAGGCTGG GGCTGGGGAG 1020 GCCTCTTACC CACCCAGGGA AGGGAGGAGC TCCTGAAGGT GATCCTTGAG CAGGTTCTAT 1080 AGAACCTATA GGCAGCTGCT TCTGGGAGCC GCTGCAGAAA AGGGGGAACA CTGGTGGTGA 1140 GGCCCTGCCA GCCTGGGGGT GGGGTCTCGA ATACTACTGG GCCATAGCAA CCCCCACACC 1200 CACTCTGCCC CTAGCTCCCC TGACTTCCCA AAGCCAAAGC TTCCTTCCTC CCCCATCCCC 1260 ACTCCTCCAG TAGACTTCCC CTTTCCAAAC CCCCTGCTGT TCCCGCCAAA CACGCAGGCA 1320 GGCATACCCA CCCTTGTGTC AATCCCGTAC CTCCCCACGT GCCACCTGCC AGCCAAATCC 1380 CATCACCTTC GGGATCCGTC 1400
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