Tag | Content |
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EnhancerAtlas ID | HS037-17582 |
Organism | Homo sapiens |
Tissue/cell | ESC |
Coordinate | chr19:14473840-14475100 |
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 | AAATACAAAA AATTAGCCGG GCGTGGTGGG GGGCGCCTGT AGCCCCAGCT ACTCGGGAGG 60 CTGAGGCAGG AGAATGGCGT GAACCTGGGA GGCAGAGCTT GCAGTGAGCC GAGATCGCGC 120 CACTGCACTC CAGCCTGGGT GACAGAGCAA GACTCCGTCT CAAAAAAAAA AGAAAAAAGA 180 AAAAAAAGGA AGGAACAAGG CTCAGAGAGG TCCAAGGAGT TGCCCTGGCG GTCCGGGGCC 240 ACAGTGGCCT TCATCCCCAG CTGAGATGTG TCCCCAGTCT AAGGCCACTC AGAGCCAGGC 300 ACCTTCTCCG GCTGCCTCCC AATCCCCGCC CCCCGCTTCC GTCCCAGCAC CCTCACCCCG 360 CCCCCGGGCC CCTTTGTCCT CCTCTTCGTC TTATTTCCAG AATTTCTCCT CCCTAGGGAA 420 TCCAGTCCAT GTGCTTTTGA TTCCTTTGTC CTGAACTCAT GCGGCATGAG CACCCCTGAA 480 GCCTTATGTG GAAAAATTTG GAGGCTGGGG GTGGGGAGGG GGTCACATTC CTCCCGGGGG 540 TACAGAGCTA CGTCGGCATC TCCAGGGCCC CCCAGCAGCA AGCAGGCATC CTCCCAGGCC 600 AGGCCAGACC GGACGCTGCC CAACACAGGC TTTCTTTGGG GCTTGGCCGG CGCCCGACTA 660 CAGCCCCGGC TCCAGCTGCC CTGCCTGTCC CCCGCCCCCA CGCCTCCCGT CCCAACCTCC 720 CACACGTTTC CTCCTAGAAG CCCAGACCCG TGGGACTTGG CCTCCCCCGC GCCTTCCCTC 780 TCTACTCAGC TCTGCAGCTC CTGTAGGCCT CCTCCCCGGG TGATCACAGA AGGACCAGCT 840 CACCTTAGCG GGACAGGCAG GGCATGGGCG TGGCCAGAGC CTCGGGCAGG CATCCCAGGC 900 TCCCTGGTGT CTCTCTCATC CGCTGGCCTC TGTGCCCTCT TCTCTTCCCC ACCCCCGCTC 960 GTGGCCCCTC CTGCCTCTCC ATCGCAAAGT CCCCAGAGGA GTCTCCTTAA TCACTTGCTT 1020 TTGACTGAAT CCTGACCACC TGGACCCTGA TCTAGCTACT GAGGAGATAA AGTAACCAAC 1080 ACTTAAAAGC TAACCTTCAG GCATTCTGGG AGGCTGAGAC TGACGGATCA CTTGAGGTCA 1140 GGAGTTCAAG ACCAGCCTGG CCAACAAGAT GAAACCTCGT CTCTACTAAA AATACAAAAA 1200 AATTAGCTGG CGTAGTGGCG GATGCCTGTA ATCCCAGCTA CTGCGGAGGC TGAGGCAGGA 1260
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