Tag | Content |
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EnhancerAtlas ID | HS007-08095 |
Organism | Homo sapiens |
Tissue/cell | BE2C |
Coordinate | chr19:14473940-14475150 |
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 | GCAGTGAGCC GAGATCGCGC CACTGCACTC CAGCCTGGGT GACAGAGCAA GACTCCGTCT 60 CAAAAAAAAA AGAAAAAAGA AAAAAAAGGA AGGAACAAGG CTCAGAGAGG TCCAAGGAGT 120 TGCCCTGGCG GTCCGGGGCC ACAGTGGCCT TCATCCCCAG CTGAGATGTG TCCCCAGTCT 180 AAGGCCACTC AGAGCCAGGC ACCTTCTCCG GCTGCCTCCC AATCCCCGCC CCCCGCTTCC 240 GTCCCAGCAC CCTCACCCCG CCCCCGGGCC CCTTTGTCCT CCTCTTCGTC TTATTTCCAG 300 AATTTCTCCT CCCTAGGGAA TCCAGTCCAT GTGCTTTTGA TTCCTTTGTC CTGAACTCAT 360 GCGGCATGAG CACCCCTGAA GCCTTATGTG GAAAAATTTG GAGGCTGGGG GTGGGGAGGG 420 GGTCACATTC CTCCCGGGGG TACAGAGCTA CGTCGGCATC TCCAGGGCCC CCCAGCAGCA 480 AGCAGGCATC CTCCCAGGCC AGGCCAGACC GGACGCTGCC CAACACAGGC TTTCTTTGGG 540 GCTTGGCCGG CGCCCGACTA CAGCCCCGGC TCCAGCTGCC CTGCCTGTCC CCCGCCCCCA 600 CGCCTCCCGT CCCAACCTCC CACACGTTTC CTCCTAGAAG CCCAGACCCG TGGGACTTGG 660 CCTCCCCCGC GCCTTCCCTC TCTACTCAGC TCTGCAGCTC CTGTAGGCCT CCTCCCCGGG 720 TGATCACAGA AGGACCAGCT CACCTTAGCG GGACAGGCAG GGCATGGGCG TGGCCAGAGC 780 CTCGGGCAGG CATCCCAGGC TCCCTGGTGT CTCTCTCATC CGCTGGCCTC TGTGCCCTCT 840 TCTCTTCCCC ACCCCCGCTC GTGGCCCCTC CTGCCTCTCC ATCGCAAAGT CCCCAGAGGA 900 GTCTCCTTAA TCACTTGCTT TTGACTGAAT CCTGACCACC TGGACCCTGA TCTAGCTACT 960 GAGGAGATAA AGTAACCAAC ACTTAAAAGC TAACCTTCAG GCATTCTGGG AGGCTGAGAC 1020 TGACGGATCA CTTGAGGTCA GGAGTTCAAG ACCAGCCTGG CCAACAAGAT GAAACCTCGT 1080 CTCTACTAAA AATACAAAAA AATTAGCTGG CGTAGTGGCG GATGCCTGTA ATCCCAGCTA 1140 CTGCGGAGGC TGAGGCAGGA GAATCGCTTG AACTTGGGAG GTGGAGATTG CAGTGAGCTG 1200 AGATCGTGCC 1210
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