Tag | Content |
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EnhancerAtlas ID | HS092-22504 |
Organism | Homo sapiens |
Tissue/cell | HFF |
Coordinate | chr19:14473870-14475170 |
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 | GGGCGCCTGT AGCCCCAGCT ACTCGGGAGG CTGAGGCAGG AGAATGGCGT GAACCTGGGA 60 GGCAGAGCTT GCAGTGAGCC GAGATCGCGC CACTGCACTC CAGCCTGGGT GACAGAGCAA 120 GACTCCGTCT CAAAAAAAAA AGAAAAAAGA AAAAAAAGGA AGGAACAAGG CTCAGAGAGG 180 TCCAAGGAGT TGCCCTGGCG GTCCGGGGCC ACAGTGGCCT TCATCCCCAG CTGAGATGTG 240 TCCCCAGTCT AAGGCCACTC AGAGCCAGGC ACCTTCTCCG GCTGCCTCCC AATCCCCGCC 300 CCCCGCTTCC GTCCCAGCAC CCTCACCCCG CCCCCGGGCC CCTTTGTCCT CCTCTTCGTC 360 TTATTTCCAG AATTTCTCCT CCCTAGGGAA TCCAGTCCAT GTGCTTTTGA TTCCTTTGTC 420 CTGAACTCAT GCGGCATGAG CACCCCTGAA GCCTTATGTG GAAAAATTTG GAGGCTGGGG 480 GTGGGGAGGG GGTCACATTC CTCCCGGGGG TACAGAGCTA CGTCGGCATC TCCAGGGCCC 540 CCCAGCAGCA AGCAGGCATC CTCCCAGGCC AGGCCAGACC GGACGCTGCC CAACACAGGC 600 TTTCTTTGGG GCTTGGCCGG CGCCCGACTA CAGCCCCGGC TCCAGCTGCC CTGCCTGTCC 660 CCCGCCCCCA CGCCTCCCGT CCCAACCTCC CACACGTTTC CTCCTAGAAG CCCAGACCCG 720 TGGGACTTGG CCTCCCCCGC GCCTTCCCTC TCTACTCAGC TCTGCAGCTC CTGTAGGCCT 780 CCTCCCCGGG TGATCACAGA AGGACCAGCT CACCTTAGCG GGACAGGCAG GGCATGGGCG 840 TGGCCAGAGC CTCGGGCAGG CATCCCAGGC TCCCTGGTGT CTCTCTCATC CGCTGGCCTC 900 TGTGCCCTCT TCTCTTCCCC ACCCCCGCTC GTGGCCCCTC CTGCCTCTCC ATCGCAAAGT 960 CCCCAGAGGA GTCTCCTTAA TCACTTGCTT TTGACTGAAT CCTGACCACC TGGACCCTGA 1020 TCTAGCTACT GAGGAGATAA AGTAACCAAC ACTTAAAAGC TAACCTTCAG GCATTCTGGG 1080 AGGCTGAGAC TGACGGATCA CTTGAGGTCA GGAGTTCAAG ACCAGCCTGG CCAACAAGAT 1140 GAAACCTCGT CTCTACTAAA AATACAAAAA AATTAGCTGG CGTAGTGGCG GATGCCTGTA 1200 ATCCCAGCTA CTGCGGAGGC TGAGGCAGGA GAATCGCTTG AACTTGGGAG GTGGAGATTG 1260 CAGTGAGCTG AGATCGTGCC ACTGCACTCC AGCCTGGGCA 1300
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