Tag | Content |
---|
EnhancerAtlas ID | HS086-00139 |
Organism | Homo sapiens |
Tissue/cell | HEK293 |
Coordinate | chr1:6660060-6661850 |
Target genes | Number: 17 | Name | Ensembl ID |
|
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Nfe2l2 | MA0150.2 | chr1:6661244-6661259 | TACCATGACTCGGCA | + | 6.41 |
|
| 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 |
|
| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | GAAGCTGTGT AAGTATAATA TATATATATA TATTCTTCTG CCTGTATTAT TATTATTATT 60 TTTGAGACAG AGTCTTGCTC TGTCACCCAG ACTGGAGTGC AGCGGCATGA TCTCAGCTTA 120 CTGCAACCTC CACCTCCTGG GCTCAAGCAA TCCTCCCACC TCAGCCTCCT GAGTGGCTGG 180 GACAACAGGC ACATGCCGCC ACACCCAGCT AATTTTTGTA TTTTTTGTAC AGACGGGGTT 240 TCGCCATGTT GTCCAGGCTG GTCTCGAACT CCTGAGCTGA AGTGATCCAC CCACCTTGAT 300 ATCCCAAAGT GCTGGGATTA CAAAGAGCCA CTGCACCCGG CCCGTATTTT CAATTTCAAT 360 AAAAAGCTAA GAATAAAAAG TGGTACTGGC TGTAATCGTA AATTACACCA GGTCTATTAG 420 AAACCCCAGG ACATGAAGGG ACCCCAAGCA TCCTGGGGGC TGTACCCCTT GGCCTCCCAG 480 GCTGGCGCCA CAGGACAGAG CGGACAAGAC ATTCTGTTTC ACAGCCCTGA GCTCTAAAGG 540 GAGAAAAGCA AGTTCTTGTT CTTAGGAAGT GAGCTCTGCC GGCCTCCTCC CTTCCATGGA 600 GCTGTGTGAA AGGCAGCTGA AAGGAATGAA CCAGCCACCT GCCTAAACCC AAGGGATTAA 660 CTGCTCTGCT GGGACATTTA TGGAAGGGTG TGCAGAAAGC TGGGGCCAGT GTGGCCAGTT 720 CTGGGAAGAA ATTATCTGCT CAAAGCCACT GGTCAGACTT TCAGAAGAGG GGAGGGACAC 780 GGTCCCCAAT CAACTTGGGG ACAACCTTGG ATTGGAAAGA GGCACAGATT CTGGCAGAAC 840 CCAGCAGAGG CTGGACTCAG AGCAGCAGGC TAAGGAAGCT GTGGCAACAG AATCCAGCAA 900 CTGTCCCACC TGACACCTCA GAGCCCCACT GGAACTCGGA GCACGTCCCA GAGTGGGCTC 960 TCTCGCGAAC ATGCAAGGCT GGGCACAGCA GCTGTGACAT CCCAGTCCCC ACCTCCTTGC 1020 CTGATAACCG CCTCACACGC CTGCCTGGTG GGTTCTTTCC TTATATAGCA GTCACAGAGA 1080 CCGCCCTTCC TCACCCCGAC AAAGGAGGTA GCCTCGTGTT TGAACTGGGA TTTATCTTTA 1140 ATAAAAACCG TAGAAGCCCA AACTCAGGCG GACTGGGACC CGCCTACCAT GACTCGGCAG 1200 TGTTTTGGGG TTTGGGCCAA GTAACTGGAA GAAAACCTCT TAACATGTGA CCATGTTTAC 1260 AGGCTCCGGG GAGTTCAGCC TAAACACCAT GTGACCAGAG CACAGAGCCT AGGTGCAAGC 1320 CCAAGGGAAC CTTGTCACCG GGTGACAAAG AGTGAGTCAG GGGGCCCGGT GTGGCTCAGC 1380 AGGGAGGGAG AAATTCCCCG GCTTGTGGGG AACAGATGCC TCACCGGGCG TCGGCCTCCT 1440 GCCCGTCCCT GGATTCCTTA AGGAGAAAAA GAAAGCACCC ATTGTGCGGG GTGAATGCCC 1500 CAGTATCTTC CAACCAAGTG GGGAGGCACC TCCTGGGCAC GGAGTTGGCT CAGCCTGGCA 1560 GCCCCGGCCG CACGGGGCAC AGAGACCCAC AAGCAGCTAC TTGTCCCGGC TCACACAAGG 1620 GGCCCTTCTT CAAGGTTAAA AGTATCGCCC AGAGACATGT AGTCACCAGA GCCCCAGCTT 1680 GGACTCAGGT GCGCCCCTAG GATTCCAGGC TCTGTGCGCT TCCCCCGCGA ATAGCTGGGC 1740 TCCCGTACCG GCGAGGTTCA ACCCCAGAGA GCCTGCCCAG CCCCTGGCCC 1790
|