Tag | Content |
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EnhancerAtlas ID | HS059-00142 |
Organism | Homo sapiens |
Tissue/cell | GM12878 |
Coordinate | chr1:6660340-6661850 |
Target genes | Number: 13 | Name | Ensembl ID |
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SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Nfe2l2 | MA0150.2 | chr1:6661244-6661259 | TACCATGACTCGGCA | + | 6.41 |
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| Number of super-enhancer constituents: 32 | ID | Coordinate | Tissue/cell |
SE_01053 | chr1:6660448-6664624 | Adrenal_Gland | SE_01890 | chr1:6660238-6664639 | Aorta | SE_03093 | chr1:6660589-6664743 | Bladder | SE_04553 | chr1:6658786-6663024 | Brain_Anterior_Caudate | SE_07317 | chr1:6659027-6665174 | Brain_Hippocampus_Middle_150 | SE_09798 | chr1:6658598-6665201 | CD14 | SE_15124 | chr1:6659045-6665168 | CD4_Memory_Primary_7pool | SE_19050 | chr1:6658603-6665131 | CD4p_CD25-_Il17-_PMAstim_Th | SE_19297 | chr1:6658880-6664820 | CD4p_CD25-_Il17p_PMAstim_Th17 | SE_21108 | chr1:6659182-6665098 | CD8_Memory_7pool | SE_24407 | chr1:6660609-6664237 | Colon_Crypt_2 | SE_26672 | chr1:6658859-6665356 | Esophagus | SE_30037 | chr1:6660076-6665829 | Fetal_Muscle | SE_31935 | chr1:6660216-6665326 | Gastric | SE_36216 | chr1:6658652-6665086 | HMEC | SE_40051 | chr1:6659129-6664881 | K562 | SE_40857 | chr1:6658849-6665628 | Left_Ventricle | SE_42593 | chr1:6658924-6665759 | Lung | SE_45247 | chr1:6660268-6665287 | NHLF | SE_46994 | chr1:6660425-6661222 | Ovary | SE_46994 | chr1:6661281-6662966 | Ovary | SE_47873 | chr1:6660460-6664607 | Pancreas | SE_48309 | chr1:6658831-6665412 | Psoas_Muscle | SE_48826 | chr1:6660234-6665814 | Right_Atrium | SE_49618 | chr1:6660361-6662986 | Right_Ventricle | SE_50723 | chr1:6660229-6665339 | Sigmoid_Colon | SE_51326 | chr1:6656436-6665828 | Skeletal_Muscle | SE_53119 | chr1:6660211-6665398 | Small_Intestine | SE_53559 | chr1:6658837-6665348 | Spleen | SE_54804 | chr1:6659286-6665727 | Stomach_Smooth_Muscle | SE_58743 | chr1:6616886-6664806 | Ly1 | SE_64785 | chr1:6658809-6662937 | NHEK |
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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 | AGTGATCCAC CCACCTTGAT ATCCCAAAGT GCTGGGATTA CAAAGAGCCA CTGCACCCGG 60 CCCGTATTTT CAATTTCAAT AAAAAGCTAA GAATAAAAAG TGGTACTGGC TGTAATCGTA 120 AATTACACCA GGTCTATTAG AAACCCCAGG ACATGAAGGG ACCCCAAGCA TCCTGGGGGC 180 TGTACCCCTT GGCCTCCCAG GCTGGCGCCA CAGGACAGAG CGGACAAGAC ATTCTGTTTC 240 ACAGCCCTGA GCTCTAAAGG GAGAAAAGCA AGTTCTTGTT CTTAGGAAGT GAGCTCTGCC 300 GGCCTCCTCC CTTCCATGGA GCTGTGTGAA AGGCAGCTGA AAGGAATGAA CCAGCCACCT 360 GCCTAAACCC AAGGGATTAA CTGCTCTGCT GGGACATTTA TGGAAGGGTG TGCAGAAAGC 420 TGGGGCCAGT GTGGCCAGTT CTGGGAAGAA ATTATCTGCT CAAAGCCACT GGTCAGACTT 480 TCAGAAGAGG GGAGGGACAC GGTCCCCAAT CAACTTGGGG ACAACCTTGG ATTGGAAAGA 540 GGCACAGATT CTGGCAGAAC CCAGCAGAGG CTGGACTCAG AGCAGCAGGC TAAGGAAGCT 600 GTGGCAACAG AATCCAGCAA CTGTCCCACC TGACACCTCA GAGCCCCACT GGAACTCGGA 660 GCACGTCCCA GAGTGGGCTC TCTCGCGAAC ATGCAAGGCT GGGCACAGCA GCTGTGACAT 720 CCCAGTCCCC ACCTCCTTGC CTGATAACCG CCTCACACGC CTGCCTGGTG GGTTCTTTCC 780 TTATATAGCA GTCACAGAGA CCGCCCTTCC TCACCCCGAC AAAGGAGGTA GCCTCGTGTT 840 TGAACTGGGA TTTATCTTTA ATAAAAACCG TAGAAGCCCA AACTCAGGCG GACTGGGACC 900 CGCCTACCAT GACTCGGCAG TGTTTTGGGG TTTGGGCCAA GTAACTGGAA GAAAACCTCT 960 TAACATGTGA CCATGTTTAC AGGCTCCGGG GAGTTCAGCC TAAACACCAT GTGACCAGAG 1020 CACAGAGCCT AGGTGCAAGC CCAAGGGAAC CTTGTCACCG GGTGACAAAG AGTGAGTCAG 1080 GGGGCCCGGT GTGGCTCAGC AGGGAGGGAG AAATTCCCCG GCTTGTGGGG AACAGATGCC 1140 TCACCGGGCG TCGGCCTCCT GCCCGTCCCT GGATTCCTTA AGGAGAAAAA GAAAGCACCC 1200 ATTGTGCGGG GTGAATGCCC CAGTATCTTC CAACCAAGTG GGGAGGCACC TCCTGGGCAC 1260 GGAGTTGGCT CAGCCTGGCA GCCCCGGCCG CACGGGGCAC AGAGACCCAC AAGCAGCTAC 1320 TTGTCCCGGC TCACACAAGG GGCCCTTCTT CAAGGTTAAA AGTATCGCCC AGAGACATGT 1380 AGTCACCAGA GCCCCAGCTT GGACTCAGGT GCGCCCCTAG GATTCCAGGC TCTGTGCGCT 1440 TCCCCCGCGA ATAGCTGGGC TCCCGTACCG GCGAGGTTCA ACCCCAGAGA GCCTGCCCAG 1500 CCCCTGGCCC 1510
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