Tag | Content |
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EnhancerAtlas ID | HS154-11011 |
Organism | Homo sapiens |
Tissue/cell | Osteoblast |
Coordinate | chr19:14474060-14475090 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Nr2f6(var.2) | MA0728.1 | chr19:14474973-14474988 | GAGGTCAGGAGTTCA | + | 6.22 | SP4 | MA0685.1 | chr19:14474700-14474717 | GGCATGGGCGTGGCCAG | - | 6.02 | ZNF263 | MA0528.1 | chr19:14474339-14474360 | GGAGGCTGGGGGTGGGGAGGG | + | 6.01 |
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| Number of super-enhancer constituents: 26 | ID | Coordinate | Tissue/cell |
SE_09406 | chr19:14473828-14474954 | CD14 | SE_10220 | chr19:14473866-14475110 | CD19_Primary | SE_10950 | chr19:14472405-14476345 | CD20 | SE_11837 | chr19:14473931-14475221 | CD3 | SE_13526 | chr19:14473863-14474894 | CD34_Primary_RO01536 | SE_14416 | chr19:14473373-14475234 | CD4_Memory_Primary_7pool | SE_15810 | chr19:14473799-14474984 | CD4_Naive_Primary_7pool | SE_16317 | chr19:14474075-14475239 | CD4_Naive_Primary_8pool | SE_16867 | chr19:14473866-14475099 | CD4p_CD225int_CD127p_Tmem | SE_17824 | chr19:14473345-14475249 | CD4p_CD25-_CD45ROp_Memory | SE_18377 | chr19:14472467-14476404 | CD4p_CD25-_Il17-_PMAstim_Th | SE_19159 | chr19:14473633-14475114 | CD4p_CD25-_Il17p_PMAstim_Th17 | SE_19988 | chr19:14472673-14475105 | CD56 | SE_20741 | chr19:14473788-14475063 | CD8_Memory_7pool | SE_21447 | chr19:14473803-14475032 | CD8_Naive_7pool | SE_21965 | chr19:14473801-14474965 | CD8_Naive_8pool | SE_22295 | chr19:14473360-14475242 | CD8_primiary | SE_23938 | chr19:14474196-14474847 | Colon_Crypt_2 | SE_30750 | chr19:14474014-14475011 | Fetal_Muscle | SE_40289 | chr19:14473871-14475217 | K562 | SE_42847 | chr19:14473903-14475159 | Lung | SE_50325 | chr19:14473906-14475074 | Sigmoid_Colon | SE_52719 | chr19:14473913-14475083 | Small_Intestine | SE_53468 | chr19:14472613-14475254 | Spleen | SE_55331 | chr19:14474221-14475011 | Thymus | SE_62560 | chr19:14458771-14497116 | Tonsil |
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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 | TGCCCTGGCG GTCCGGGGCC ACAGTGGCCT TCATCCCCAG CTGAGATGTG TCCCCAGTCT 60 AAGGCCACTC AGAGCCAGGC ACCTTCTCCG GCTGCCTCCC AATCCCCGCC CCCCGCTTCC 120 GTCCCAGCAC CCTCACCCCG CCCCCGGGCC CCTTTGTCCT CCTCTTCGTC TTATTTCCAG 180 AATTTCTCCT CCCTAGGGAA TCCAGTCCAT GTGCTTTTGA TTCCTTTGTC CTGAACTCAT 240 GCGGCATGAG CACCCCTGAA GCCTTATGTG GAAAAATTTG GAGGCTGGGG GTGGGGAGGG 300 GGTCACATTC CTCCCGGGGG TACAGAGCTA CGTCGGCATC TCCAGGGCCC CCCAGCAGCA 360 AGCAGGCATC CTCCCAGGCC AGGCCAGACC GGACGCTGCC CAACACAGGC TTTCTTTGGG 420 GCTTGGCCGG CGCCCGACTA CAGCCCCGGC TCCAGCTGCC CTGCCTGTCC CCCGCCCCCA 480 CGCCTCCCGT CCCAACCTCC CACACGTTTC CTCCTAGAAG CCCAGACCCG TGGGACTTGG 540 CCTCCCCCGC GCCTTCCCTC TCTACTCAGC TCTGCAGCTC CTGTAGGCCT CCTCCCCGGG 600 TGATCACAGA AGGACCAGCT CACCTTAGCG GGACAGGCAG GGCATGGGCG TGGCCAGAGC 660 CTCGGGCAGG CATCCCAGGC TCCCTGGTGT CTCTCTCATC CGCTGGCCTC TGTGCCCTCT 720 TCTCTTCCCC ACCCCCGCTC GTGGCCCCTC CTGCCTCTCC ATCGCAAAGT CCCCAGAGGA 780 GTCTCCTTAA TCACTTGCTT TTGACTGAAT CCTGACCACC TGGACCCTGA TCTAGCTACT 840 GAGGAGATAA AGTAACCAAC ACTTAAAAGC TAACCTTCAG GCATTCTGGG AGGCTGAGAC 900 TGACGGATCA CTTGAGGTCA GGAGTTCAAG ACCAGCCTGG CCAACAAGAT GAAACCTCGT 960 CTCTACTAAA AATACAAAAA AATTAGCTGG CGTAGTGGCG GATGCCTGTA ATCCCAGCTA 1020 CTGCGGAGGC 1030
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