Tag | Content |
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EnhancerAtlas ID | HS051-13832 |
Organism | Homo sapiens |
Tissue/cell | Fetal_thymus |
Coordinate | chr19:14473950-14475120 |
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 | GAGATCGCGC CACTGCACTC CAGCCTGGGT GACAGAGCAA GACTCCGTCT CAAAAAAAAA 60 AGAAAAAAGA AAAAAAAGGA AGGAACAAGG CTCAGAGAGG TCCAAGGAGT TGCCCTGGCG 120 GTCCGGGGCC ACAGTGGCCT TCATCCCCAG CTGAGATGTG TCCCCAGTCT AAGGCCACTC 180 AGAGCCAGGC ACCTTCTCCG GCTGCCTCCC AATCCCCGCC CCCCGCTTCC GTCCCAGCAC 240 CCTCACCCCG CCCCCGGGCC CCTTTGTCCT CCTCTTCGTC TTATTTCCAG AATTTCTCCT 300 CCCTAGGGAA TCCAGTCCAT GTGCTTTTGA TTCCTTTGTC CTGAACTCAT GCGGCATGAG 360 CACCCCTGAA GCCTTATGTG GAAAAATTTG GAGGCTGGGG GTGGGGAGGG GGTCACATTC 420 CTCCCGGGGG TACAGAGCTA CGTCGGCATC TCCAGGGCCC CCCAGCAGCA AGCAGGCATC 480 CTCCCAGGCC AGGCCAGACC GGACGCTGCC CAACACAGGC TTTCTTTGGG GCTTGGCCGG 540 CGCCCGACTA CAGCCCCGGC TCCAGCTGCC CTGCCTGTCC CCCGCCCCCA CGCCTCCCGT 600 CCCAACCTCC CACACGTTTC CTCCTAGAAG CCCAGACCCG TGGGACTTGG CCTCCCCCGC 660 GCCTTCCCTC TCTACTCAGC TCTGCAGCTC CTGTAGGCCT CCTCCCCGGG TGATCACAGA 720 AGGACCAGCT CACCTTAGCG GGACAGGCAG GGCATGGGCG TGGCCAGAGC CTCGGGCAGG 780 CATCCCAGGC TCCCTGGTGT CTCTCTCATC CGCTGGCCTC TGTGCCCTCT TCTCTTCCCC 840 ACCCCCGCTC GTGGCCCCTC CTGCCTCTCC ATCGCAAAGT CCCCAGAGGA GTCTCCTTAA 900 TCACTTGCTT TTGACTGAAT CCTGACCACC TGGACCCTGA TCTAGCTACT GAGGAGATAA 960 AGTAACCAAC ACTTAAAAGC TAACCTTCAG GCATTCTGGG AGGCTGAGAC TGACGGATCA 1020 CTTGAGGTCA GGAGTTCAAG ACCAGCCTGG CCAACAAGAT GAAACCTCGT CTCTACTAAA 1080 AATACAAAAA AATTAGCTGG CGTAGTGGCG GATGCCTGTA ATCCCAGCTA CTGCGGAGGC 1140 TGAGGCAGGA GAATCGCTTG AACTTGGGAG 1170
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