Tag | Content |
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EnhancerAtlas ID | HS170-02565 |
Organism | Homo sapiens |
Tissue/cell | RS4-11 |
Coordinate | chr22:31682010-31683280 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOXP1 | MA0481.2 | chr22:31682254-31682266 | TTCTGTTTACAT | - | 6.92 | FOXP2 | MA0593.1 | chr22:31682255-31682266 | TCTGTTTACAT | - | 6.02 |
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| Number of super-enhancer constituents: 29 | ID | Coordinate | Tissue/cell |
SE_03824 | chr22:31682525-31683008 | Brain_Angular_Gyrus | SE_04681 | chr22:31680198-31683330 | Brain_Anterior_Caudate | SE_08687 | chr22:31679936-31683212 | Brain_Inferior_Temporal_Lobe | SE_10797 | chr22:31680149-31688920 | CD19_Primary | SE_11287 | chr22:31677460-31690340 | CD20 | SE_12107 | chr22:31680117-31689115 | CD3 | SE_14631 | chr22:31680015-31690177 | CD4_Memory_Primary_7pool | SE_15464 | chr22:31681154-31683339 | CD4_Memory_Primary_8pool | SE_15871 | chr22:31680696-31683337 | CD4_Naive_Primary_7pool | SE_16377 | chr22:31681343-31683359 | CD4_Naive_Primary_8pool | SE_17035 | chr22:31682070-31683323 | CD4p_CD225int_CD127p_Tmem | SE_17430 | chr22:31672956-31691036 | CD4p_CD25-_CD45RAp_Naive | SE_17977 | chr22:31679828-31690556 | CD4p_CD25-_CD45ROp_Memory | SE_18592 | chr22:31673282-31693670 | CD4p_CD25-_Il17-_PMAstim_Th | SE_19595 | chr22:31680056-31683311 | CD4p_CD25-_Il17p_PMAstim_Th17 | SE_20431 | chr22:31680155-31689069 | CD56 | SE_20993 | chr22:31680049-31683336 | CD8_Memory_7pool | SE_21528 | chr22:31680472-31690255 | CD8_Naive_7pool | SE_21928 | chr22:31679942-31690434 | CD8_Naive_8pool | SE_22539 | chr22:31680014-31690130 | CD8_primiary | SE_24209 | chr22:31682622-31683000 | Colon_Crypt_2 | SE_27355 | chr22:31682408-31683224 | Esophagus | SE_31999 | chr22:31682012-31683335 | Gastric | SE_42312 | chr22:31682296-31683229 | Lung | SE_50393 | chr22:31680023-31683217 | Sigmoid_Colon | SE_52405 | chr22:31680170-31683201 | Small_Intestine | SE_53858 | chr22:31680049-31689083 | Spleen | SE_55166 | chr22:31680339-31683389 | Thymus | SE_62272 | chr22:31668337-31710103 | Tonsil |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 3 | Chromosome | Start | End |
chr22 | 31682273 | 31682394 | chr22 | 31682154 | 31683004 | chr22 | 31682400 | 31683104 |
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Enhancer Sequence | TAGCAGGACA TGGTGGCGGG TGCCTCTAAT CCCAGCTACT CGGGAGGCTG AGGCAGGAGA 60 ATCACTTGAA CCCAGGAGGC GGCGGTTGCA GTGAGCCGAC ACAGCGAGAC TCTGTCTCAA 120 AAAAAAAAAA ATTAAGAAAA AAAGATAATC AGGGAAGAGC ATACAGTAGG GCCTTACTTA 180 TTAAGAAAGC ATGAAATAAA TGTTGGCTGC TATTGTGATT ATTACCTGAT TGGTGTGCTA 240 TTGTTTCTGT TTACATTTAA TACTTATAAT CTTAGATGGG TAGATGTGGA GGGAGGATAT 300 ATCCCCATTT AACAGACAAG ATACCAAGGC TCAGAGGGCA CCTGAACCCA CACTCAACCT 360 ACAGCTCTTT TCAGGACACT CTGCTCTCTG ACTTTAGGAA GAGATGAAGG CTGCAAGCTT 420 GTTTTTAAGC CCACATGCGG TTTCCTGTTG TACAGTCTGT TCTCAGAGCA GTTCTGCTGA 480 AGAAAGGGGT GATCTGGTCG TTAGTGACGG GGAGTCTGAT GACTGGGTGC CTTGCCCTGA 540 GTTTACAGGA AAATAAATTT TAGGCCTCAG GGCAGTCTCG TGACAGCCTA GAGGAACAAA 600 TCTAGAAGAA AAAAGACTTC CACTGGACAC CAGAACTGAG CTCAGAATTA AGAATGTTTA 660 GTCAGTTCAA GCACCTGGAA GGCCTGGAAA CTGTCACAGG ATTGCAGGAC AGCCAAATGC 720 TGTTGGGTGG CTGAGGAAAA AGGAGATAGT TCAAGGACTA AACTCAGCCA ATGTGGCTTA 780 GGTCTGCTTA TGAATTGTAA GGCCAGGGCC ACTATGTCAT TAACTCTGAA ATGAACAAGC 840 AGGTGTCCCT GGACCTGCAT GTCAAGCATC CCATTGTGGG AAACAACCTC AGACTGGGCG 900 TCAGGATGTC CTCTCAAGTC AATACTTTCC CTCTCTGGAC CTCTGCTTCC TGCATCATAA 960 GAAATCAGAG AGTACTAGTC CATTACCCAC TTTTTTTTTT TTTTTTTTTT TTTTGAGACA 1020 GCATCTCACT CTGTCACCCA GGCTGGAGTG CAGTGGCACA ATCATGGCTC ACCATAGCGA 1080 CTTCCCAGGC TCAGGTGATC CTCCCATCTC AGCCTCCTTA GTAACTAGGA CTACAGGCGC 1140 CCACCACCAT GCCTGGCTAA TTTTTGTATT TTTTTGTAGA GACAGGGTTT TGCCATGTTG 1200 CCCATGCTGG TCTCGAACTC TTGGGCTCAA GCGATCCACC CACCTCTGCC TCCCAAAGTG 1260 CTAGGATTAC 1270
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