Tag | Content |
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EnhancerAtlas ID | HS187-00072 |
Organism | Homo sapiens |
Tissue/cell | Th1 |
Coordinate | chr1:6660150-6661850 |
Target genes | Number: 15 | 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 | ACTGGAGTGC AGCGGCATGA TCTCAGCTTA CTGCAACCTC CACCTCCTGG GCTCAAGCAA 60 TCCTCCCACC TCAGCCTCCT GAGTGGCTGG GACAACAGGC ACATGCCGCC ACACCCAGCT 120 AATTTTTGTA TTTTTTGTAC AGACGGGGTT TCGCCATGTT GTCCAGGCTG GTCTCGAACT 180 CCTGAGCTGA AGTGATCCAC CCACCTTGAT ATCCCAAAGT GCTGGGATTA CAAAGAGCCA 240 CTGCACCCGG CCCGTATTTT CAATTTCAAT AAAAAGCTAA GAATAAAAAG TGGTACTGGC 300 TGTAATCGTA AATTACACCA GGTCTATTAG AAACCCCAGG ACATGAAGGG ACCCCAAGCA 360 TCCTGGGGGC TGTACCCCTT GGCCTCCCAG GCTGGCGCCA CAGGACAGAG CGGACAAGAC 420 ATTCTGTTTC ACAGCCCTGA GCTCTAAAGG GAGAAAAGCA AGTTCTTGTT CTTAGGAAGT 480 GAGCTCTGCC GGCCTCCTCC CTTCCATGGA GCTGTGTGAA AGGCAGCTGA AAGGAATGAA 540 CCAGCCACCT GCCTAAACCC AAGGGATTAA CTGCTCTGCT GGGACATTTA TGGAAGGGTG 600 TGCAGAAAGC TGGGGCCAGT GTGGCCAGTT CTGGGAAGAA ATTATCTGCT CAAAGCCACT 660 GGTCAGACTT TCAGAAGAGG GGAGGGACAC GGTCCCCAAT CAACTTGGGG ACAACCTTGG 720 ATTGGAAAGA GGCACAGATT CTGGCAGAAC CCAGCAGAGG CTGGACTCAG AGCAGCAGGC 780 TAAGGAAGCT GTGGCAACAG AATCCAGCAA CTGTCCCACC TGACACCTCA GAGCCCCACT 840 GGAACTCGGA GCACGTCCCA GAGTGGGCTC TCTCGCGAAC ATGCAAGGCT GGGCACAGCA 900 GCTGTGACAT CCCAGTCCCC ACCTCCTTGC CTGATAACCG CCTCACACGC CTGCCTGGTG 960 GGTTCTTTCC TTATATAGCA GTCACAGAGA CCGCCCTTCC TCACCCCGAC AAAGGAGGTA 1020 GCCTCGTGTT TGAACTGGGA TTTATCTTTA ATAAAAACCG TAGAAGCCCA AACTCAGGCG 1080 GACTGGGACC CGCCTACCAT GACTCGGCAG TGTTTTGGGG TTTGGGCCAA GTAACTGGAA 1140 GAAAACCTCT TAACATGTGA CCATGTTTAC AGGCTCCGGG GAGTTCAGCC TAAACACCAT 1200 GTGACCAGAG CACAGAGCCT AGGTGCAAGC CCAAGGGAAC CTTGTCACCG GGTGACAAAG 1260 AGTGAGTCAG GGGGCCCGGT GTGGCTCAGC AGGGAGGGAG AAATTCCCCG GCTTGTGGGG 1320 AACAGATGCC TCACCGGGCG TCGGCCTCCT GCCCGTCCCT GGATTCCTTA AGGAGAAAAA 1380 GAAAGCACCC ATTGTGCGGG GTGAATGCCC CAGTATCTTC CAACCAAGTG GGGAGGCACC 1440 TCCTGGGCAC GGAGTTGGCT CAGCCTGGCA GCCCCGGCCG CACGGGGCAC AGAGACCCAC 1500 AAGCAGCTAC TTGTCCCGGC TCACACAAGG GGCCCTTCTT CAAGGTTAAA AGTATCGCCC 1560 AGAGACATGT AGTCACCAGA GCCCCAGCTT GGACTCAGGT GCGCCCCTAG GATTCCAGGC 1620 TCTGTGCGCT TCCCCCGCGA ATAGCTGGGC TCCCGTACCG GCGAGGTTCA ACCCCAGAGA 1680 GCCTGCCCAG CCCCTGGCCC 1700
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