Tag | Content |
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EnhancerAtlas ID | HS105-00258 |
Organism | Homo sapiens |
Tissue/cell | IMR90 |
Coordinate | chr1:6660240-6661850 |
Target genes | Number: 16 | 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 | GACAACAGGC ACATGCCGCC ACACCCAGCT AATTTTTGTA TTTTTTGTAC AGACGGGGTT 60 TCGCCATGTT GTCCAGGCTG GTCTCGAACT CCTGAGCTGA AGTGATCCAC CCACCTTGAT 120 ATCCCAAAGT GCTGGGATTA CAAAGAGCCA CTGCACCCGG CCCGTATTTT CAATTTCAAT 180 AAAAAGCTAA GAATAAAAAG TGGTACTGGC TGTAATCGTA AATTACACCA GGTCTATTAG 240 AAACCCCAGG ACATGAAGGG ACCCCAAGCA TCCTGGGGGC TGTACCCCTT GGCCTCCCAG 300 GCTGGCGCCA CAGGACAGAG CGGACAAGAC ATTCTGTTTC ACAGCCCTGA GCTCTAAAGG 360 GAGAAAAGCA AGTTCTTGTT CTTAGGAAGT GAGCTCTGCC GGCCTCCTCC CTTCCATGGA 420 GCTGTGTGAA AGGCAGCTGA AAGGAATGAA CCAGCCACCT GCCTAAACCC AAGGGATTAA 480 CTGCTCTGCT GGGACATTTA TGGAAGGGTG TGCAGAAAGC TGGGGCCAGT GTGGCCAGTT 540 CTGGGAAGAA ATTATCTGCT CAAAGCCACT GGTCAGACTT TCAGAAGAGG GGAGGGACAC 600 GGTCCCCAAT CAACTTGGGG ACAACCTTGG ATTGGAAAGA GGCACAGATT CTGGCAGAAC 660 CCAGCAGAGG CTGGACTCAG AGCAGCAGGC TAAGGAAGCT GTGGCAACAG AATCCAGCAA 720 CTGTCCCACC TGACACCTCA GAGCCCCACT GGAACTCGGA GCACGTCCCA GAGTGGGCTC 780 TCTCGCGAAC ATGCAAGGCT GGGCACAGCA GCTGTGACAT CCCAGTCCCC ACCTCCTTGC 840 CTGATAACCG CCTCACACGC CTGCCTGGTG GGTTCTTTCC TTATATAGCA GTCACAGAGA 900 CCGCCCTTCC TCACCCCGAC AAAGGAGGTA GCCTCGTGTT TGAACTGGGA TTTATCTTTA 960 ATAAAAACCG TAGAAGCCCA AACTCAGGCG GACTGGGACC CGCCTACCAT GACTCGGCAG 1020 TGTTTTGGGG TTTGGGCCAA GTAACTGGAA GAAAACCTCT TAACATGTGA CCATGTTTAC 1080 AGGCTCCGGG GAGTTCAGCC TAAACACCAT GTGACCAGAG CACAGAGCCT AGGTGCAAGC 1140 CCAAGGGAAC CTTGTCACCG GGTGACAAAG AGTGAGTCAG GGGGCCCGGT GTGGCTCAGC 1200 AGGGAGGGAG AAATTCCCCG GCTTGTGGGG AACAGATGCC TCACCGGGCG TCGGCCTCCT 1260 GCCCGTCCCT GGATTCCTTA AGGAGAAAAA GAAAGCACCC ATTGTGCGGG GTGAATGCCC 1320 CAGTATCTTC CAACCAAGTG GGGAGGCACC TCCTGGGCAC GGAGTTGGCT CAGCCTGGCA 1380 GCCCCGGCCG CACGGGGCAC AGAGACCCAC AAGCAGCTAC TTGTCCCGGC TCACACAAGG 1440 GGCCCTTCTT CAAGGTTAAA AGTATCGCCC AGAGACATGT AGTCACCAGA GCCCCAGCTT 1500 GGACTCAGGT GCGCCCCTAG GATTCCAGGC TCTGTGCGCT TCCCCCGCGA ATAGCTGGGC 1560 TCCCGTACCG GCGAGGTTCA ACCCCAGAGA GCCTGCCCAG CCCCTGGCCC 1610
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