Tag | Content |
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EnhancerAtlas ID | HS134-18981 |
Organism | Homo sapiens |
Tissue/cell | Mesendoderm |
Coordinate | chr14:70161550-70162990 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
NFKB1 | MA0105.4 | chr14:70162686-70162699 | AGGGGAATCACCT | - | 6.22 | NFKB1 | MA0105.4 | chr14:70162686-70162699 | AGGGGAATCACCT | + | 6.5 |
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| Number of super-enhancer constituents: 29 | ID | Coordinate | Tissue/cell |
SE_00199 | chr14:70158325-70164274 | Adipose_Nuclei | SE_01046 | chr14:70160912-70162525 | Adrenal_Gland | SE_04035 | chr14:70159394-70163897 | Brain_Anterior_Caudate | SE_05532 | chr14:70158602-70163658 | Brain_Cingulate_Gyrus | SE_06072 | chr14:70159146-70163348 | Brain_Hippocampus_Middle | SE_09201 | chr14:70157798-70165068 | CD14 | SE_10939 | chr14:70153837-70165926 | CD20 | SE_13365 | chr14:70159382-70164696 | CD34_Primary_RO01536 | SE_14528 | chr14:70158830-70164923 | CD4_Memory_Primary_7pool | SE_18280 | chr14:70159056-70164904 | CD4p_CD25-_Il17-_PMAstim_Th | SE_19687 | chr14:70162210-70163935 | CD4p_CD25-_Il17p_PMAstim_Th17 | SE_25838 | chr14:70158748-70164406 | Duodenum_Smooth_Muscle | SE_26683 | chr14:70159355-70163073 | Esophagus | SE_31172 | chr14:70159291-70164212 | Fetal_Thymus | SE_31600 | chr14:70160337-70163118 | Gastric | SE_32500 | chr14:70158866-70163889 | GM12878 | SE_40492 | chr14:70159434-70165073 | K562 | SE_40959 | chr14:70159293-70163152 | Left_Ventricle | SE_41881 | chr14:70161064-70162669 | LNCaP | SE_41881 | chr14:70162692-70163072 | LNCaP | SE_42217 | chr14:70159262-70164763 | Lung | SE_50082 | chr14:70158656-70164860 | Sigmoid_Colon | SE_51685 | chr14:70161064-70164004 | Skeletal_Muscle | SE_52366 | chr14:70158705-70164858 | Small_Intestine | SE_53796 | chr14:70158680-70163100 | Spleen | SE_55602 | chr14:70161377-70162212 | Thymus | SE_58413 | chr14:70076448-70170966 | Ly1 | SE_60579 | chr14:70076514-70162614 | DHL6 | SE_62292 | chr14:70076365-70194637 | 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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| Number: 1 | ID | Chromosome | Start | End |
GH14I069692 | chr14 | 70158719 | 70170964 |
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Enhancer Sequence | TCCGAGGCCT GTCCCACCTG TCAGTTGCTG ATCTTCCGAG GAGGGCTTAG GTTGAGCCTC 60 TCTTAGGAAG GCAGTGGTGG GGGCCCGAGA AGAGCCACAG GAGGTATCCT GAGCCATGGG 120 TGGTTTCTCC CTGTGTTCTC CCACCCCAGC TCTGGTGCCA CACCCTGAAA AAGGCTTGAG 180 CTACTGCAGG CTGGCTCTCC CCCAGTGAGT GGGAAGTTCT CATGAGAAAA GGGATCCTGA 240 CTGGACAATA GGCTTCCTGT CTGACTGCTA GGAAGATTTG TCTCATAGGA GAGGAAGGTT 300 GCAAATGGCA TGAGAAACCA TCTCACTTCC CTCTCACTGC AGCCTGTTTT AGACTTGACT 360 ATTTGGCGGG ATCGGGAAGC CAGAAGGCTG GGCAGAGCCA TGGACCAGAG CAGCCCCAGG 420 TATCTCTTAA GTAGTGGGAC TCCTGCCTGT TTTCCGGCTC TCACCACAAG TCCACAGCAG 480 GAATCTGTCC CAATGCAGGA ATTTCTGCAT GGACAGGATG ATCTCTAGCC CCTCACACCT 540 TGTGCTGTAT CCAAAACCAC AATGGTTGCA GGACTTTTGC GAAGGAACCT TGGAGAGGTA 600 GTGAGGCCCG CCAACTTTAG ACAAATTTGC AAATGTCAGA AGAGATCTCA GAGGTGATCT 660 GGTTCATTGC CTTCATGTAT TGAAACTGAG GCCCAGAGTC TACGGGCAGT ACCCAGTTTG 720 TCCTTGTCAC TGGACTCTGC CATCTGTGGC TCCCTTGACA GATTATGGGT GTGAGAGAAG 780 CCTGACTCCG AGACCCTCTG ATACTGCCCA GTGCTGTGGA ATGGGAATAC AGCCTTCTGG 840 GGTTCAAATC CTAACTGTGC CACCCACCTG CTGGGTGAAA TTGAGCAAGT ATCTCAACCC 900 CTGGCTCATC TGTGTAATGC ATTGTTATGT TTCTAGAGGG TTTTTTGTGA AACTTAAATG 960 AGTTACATAT GTAAAGTGCT CAGATAGTGC CTGGCCTGTA GTCAGTGAAC ACAAGCTGTT 1020 GTTATTAGGA GGCTTCAGAA GAAACCTTTT GACCATATCA GATGTCATCA CTTGTTTTTT 1080 CTTCTTTGTA TTTGTCTGGA ATGCTCTAAT TCCAACTTGC CTGGGAGGCT TTCTTTAGGG 1140 GAATCACCTC CCCTTTGAAA AAGGCTGTTC ATACTGGGTA TAACTCTTTC TTTTATATGC 1200 TGTACGAAGT AGCTGGATGT CTCCAAAGCC ATAGGCTGAG CACATCAAAT GGGGAAATGA 1260 GCCACAAAAC AGAACCTGGC AGGTTTCCTG ATGCCCTGCC CCCCTCAGCA GGCCCCGGCT 1320 TAACTGAGTG GTCAGGCTTG CAGCTTAGAA GCCAGAGTTC CTGGTGAATC CAGCCCTGCC 1380 AATTACAAAT GTGTGGCTTG AGGCAGATCA CTCAACTCAG TTAAGCCTTA TTGTCCTTAT 1440
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