Tag | Content |
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EnhancerAtlas ID | HS046-00100 |
Organism | Homo sapiens |
Tissue/cell | Fetal_muscle_leg |
Coordinate | chr1:6660290-6661850 |
Target genes | Number: 18 | 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 | AGACGGGGTT TCGCCATGTT GTCCAGGCTG GTCTCGAACT CCTGAGCTGA AGTGATCCAC 60 CCACCTTGAT ATCCCAAAGT GCTGGGATTA CAAAGAGCCA CTGCACCCGG CCCGTATTTT 120 CAATTTCAAT AAAAAGCTAA GAATAAAAAG TGGTACTGGC TGTAATCGTA AATTACACCA 180 GGTCTATTAG AAACCCCAGG ACATGAAGGG ACCCCAAGCA TCCTGGGGGC TGTACCCCTT 240 GGCCTCCCAG GCTGGCGCCA CAGGACAGAG CGGACAAGAC ATTCTGTTTC ACAGCCCTGA 300 GCTCTAAAGG GAGAAAAGCA AGTTCTTGTT CTTAGGAAGT GAGCTCTGCC GGCCTCCTCC 360 CTTCCATGGA GCTGTGTGAA AGGCAGCTGA AAGGAATGAA CCAGCCACCT GCCTAAACCC 420 AAGGGATTAA CTGCTCTGCT GGGACATTTA TGGAAGGGTG TGCAGAAAGC TGGGGCCAGT 480 GTGGCCAGTT CTGGGAAGAA ATTATCTGCT CAAAGCCACT GGTCAGACTT TCAGAAGAGG 540 GGAGGGACAC GGTCCCCAAT CAACTTGGGG ACAACCTTGG ATTGGAAAGA GGCACAGATT 600 CTGGCAGAAC CCAGCAGAGG CTGGACTCAG AGCAGCAGGC TAAGGAAGCT GTGGCAACAG 660 AATCCAGCAA CTGTCCCACC TGACACCTCA GAGCCCCACT GGAACTCGGA GCACGTCCCA 720 GAGTGGGCTC TCTCGCGAAC ATGCAAGGCT GGGCACAGCA GCTGTGACAT CCCAGTCCCC 780 ACCTCCTTGC CTGATAACCG CCTCACACGC CTGCCTGGTG GGTTCTTTCC TTATATAGCA 840 GTCACAGAGA CCGCCCTTCC TCACCCCGAC AAAGGAGGTA GCCTCGTGTT TGAACTGGGA 900 TTTATCTTTA ATAAAAACCG TAGAAGCCCA AACTCAGGCG GACTGGGACC CGCCTACCAT 960 GACTCGGCAG TGTTTTGGGG TTTGGGCCAA GTAACTGGAA GAAAACCTCT TAACATGTGA 1020 CCATGTTTAC AGGCTCCGGG GAGTTCAGCC TAAACACCAT GTGACCAGAG CACAGAGCCT 1080 AGGTGCAAGC CCAAGGGAAC CTTGTCACCG GGTGACAAAG AGTGAGTCAG GGGGCCCGGT 1140 GTGGCTCAGC AGGGAGGGAG AAATTCCCCG GCTTGTGGGG AACAGATGCC TCACCGGGCG 1200 TCGGCCTCCT GCCCGTCCCT GGATTCCTTA AGGAGAAAAA GAAAGCACCC ATTGTGCGGG 1260 GTGAATGCCC CAGTATCTTC CAACCAAGTG GGGAGGCACC TCCTGGGCAC GGAGTTGGCT 1320 CAGCCTGGCA GCCCCGGCCG CACGGGGCAC AGAGACCCAC AAGCAGCTAC TTGTCCCGGC 1380 TCACACAAGG GGCCCTTCTT CAAGGTTAAA AGTATCGCCC AGAGACATGT AGTCACCAGA 1440 GCCCCAGCTT GGACTCAGGT GCGCCCCTAG GATTCCAGGC TCTGTGCGCT TCCCCCGCGA 1500 ATAGCTGGGC TCCCGTACCG GCGAGGTTCA ACCCCAGAGA GCCTGCCCAG CCCCTGGCCC 1560
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