Tag | Content |
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EnhancerAtlas ID | HS049-05280 |
Organism | Homo sapiens |
Tissue/cell | Fetal_spinal_cord |
Coordinate | chr22:31685800-31686950 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
NFKB1 | MA0105.4 | chr22:31685985-31685998 | AGGGGATTCCCCC | - | 6.78 | NFKB1 | MA0105.4 | chr22:31685985-31685998 | AGGGGATTCCCCC | + | 6.92 |
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| Number of super-enhancer constituents: 31 | ID | Coordinate | Tissue/cell |
SE_03824 | chr22:31684429-31686158 | Brain_Angular_Gyrus | SE_03824 | chr22:31686355-31687461 | Brain_Angular_Gyrus | SE_04681 | chr22:31683441-31690147 | Brain_Anterior_Caudate | SE_08687 | chr22:31683359-31689556 | 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 | chr22:31684275-31689775 | CD4_Memory_Primary_8pool | SE_15871 | chr22:31684575-31690000 | CD4_Naive_Primary_7pool | SE_16377 | chr22:31684249-31689428 | CD4_Naive_Primary_8pool | SE_17035 | chr22:31684266-31689513 | 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 | chr22:31684436-31690100 | CD4p_CD25-_Il17p_PMAstim_Th17 | SE_20431 | chr22:31680155-31689069 | CD56 | SE_20993 | chr22:31683379-31689484 | 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 | chr22:31685157-31688537 | Colon_Crypt_2 | SE_27355 | chr22:31683510-31689363 | Esophagus | SE_27790 | chr22:31685362-31688949 | Fetal_Intestine | SE_31999 | chr22:31684405-31688794 | Gastric | SE_42312 | chr22:31683483-31689400 | Lung | SE_50393 | chr22:31683277-31690070 | Sigmoid_Colon | SE_52405 | chr22:31683508-31689277 | Small_Intestine | SE_53858 | chr22:31680049-31689083 | Spleen | SE_55166 | chr22:31683560-31689260 | 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: 1 | Chromosome | Start | End |
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Enhancer Sequence | ACACACAACC CAAAGTCAAA TTCTGCCCCA GAGGTAAGAT CAGGCCTGAG AGGGCTGAAC 60 CATCTCAGGG ACAAGGCAAA TGAGAGAGGA AGGCCGTAGG GAAGGGCTTC TCTCCTACCT 120 CCCACGTCTT TATCTGTCCA AATCCTTGCT ATTTCCCAAG GCCCCTCTCG GTTGCGTTCT 180 TCTGCAGGGG ATTCCCCCCA CTTCTACTTC AGGAAACAAC CCATGCTTCC TTTGAGCAGC 240 TCACATCTAA GCGTACGCTC TGTGCCAGTC CTTAGGTAAA ATGTTTTACT TTGTGCCGGG 300 AGCGGTGGCT CACGCCTGTA ATCCCAGCAC TTTGGGAGGC CAGACGGTCG GATCACCTGA 360 GGTCAGGAGT TAGAGAGCAG CCCGGCCAAC ATGGTGAAAC CCCGTCTCTA CTAAAAATAC 420 AAAAATTAGC TGGGCGTGGT GGTGCACGCC TGTTATCCCA GCTACTCAAG CGGCTGAGGC 480 AGGAGAATCA CTGTAACGCG GAAGGCGGAA GTTGCAGTGA GCCGAAATTG CGCCACTGCA 540 CTCCAGCCTG GGTGACAGAA CGAGACTCCG TCTCAAAAAA TAAAAAATAA AAAATAAATG 600 CTTTATTTTG ATTATCCCAT TTAAACCTAG AAAACTCTCT TGCTGCTTTG GGAGCAAAAA 660 GCCTGCGCTC TGGAATCTAA GAAACGTGAA TTCAAATCTG TCCCCTGCCA TTGCCTTTGG 720 TAAATCGCTT AACTTCTCTG AAGCTCAGAT GCCTCAAACG ACTTCTTCCC GCGGTGTGTG 780 TCAGGGGAGG TTGGGGAGCT GGGGTTGTGA GCAGTGTGGG TCTAGCACAC TGCAGACGCT 840 CCGCAAACGG TCAATAAACG CTGAGGGGCC AAAAGCCACT CCTCAGGACG CGCGGCGGAG 900 AGACCTAGCC TCACCCCAGC CTCGCCCCGC GCAGTTGTTT ACAAGCGCTC GCGGCGGATG 960 AGCTCATACG AGTGGCGGCG GCGGCCAATA GGCTTTGAGC CCCGCGGCCT GGAGACAGCC 1020 CTGGCCAATC GGACGGCGCG GAGGCGGAGC GGGGCCGGCC GGCATCGCGC GGCCGCACGT 1080 GCGCCACGAG TGTCTCAGCC GCTTCCTGTC AGCGCCAGGA GCGGGGATTC CCGGGGTCCC 1140 GGGCAGGTAC 1150
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