Tag | Content |
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EnhancerAtlas ID | HS053-00129 |
Organism | Homo sapiens |
Tissue/cell | Foreskin_keratinocyte |
Coordinate | chr1:6660380-6661850 |
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 | CAAAGAGCCA CTGCACCCGG CCCGTATTTT CAATTTCAAT AAAAAGCTAA GAATAAAAAG 60 TGGTACTGGC TGTAATCGTA AATTACACCA GGTCTATTAG AAACCCCAGG ACATGAAGGG 120 ACCCCAAGCA TCCTGGGGGC TGTACCCCTT GGCCTCCCAG GCTGGCGCCA CAGGACAGAG 180 CGGACAAGAC ATTCTGTTTC ACAGCCCTGA GCTCTAAAGG GAGAAAAGCA AGTTCTTGTT 240 CTTAGGAAGT GAGCTCTGCC GGCCTCCTCC CTTCCATGGA GCTGTGTGAA AGGCAGCTGA 300 AAGGAATGAA CCAGCCACCT GCCTAAACCC AAGGGATTAA CTGCTCTGCT GGGACATTTA 360 TGGAAGGGTG TGCAGAAAGC TGGGGCCAGT GTGGCCAGTT CTGGGAAGAA ATTATCTGCT 420 CAAAGCCACT GGTCAGACTT TCAGAAGAGG GGAGGGACAC GGTCCCCAAT CAACTTGGGG 480 ACAACCTTGG ATTGGAAAGA GGCACAGATT CTGGCAGAAC CCAGCAGAGG CTGGACTCAG 540 AGCAGCAGGC TAAGGAAGCT GTGGCAACAG AATCCAGCAA CTGTCCCACC TGACACCTCA 600 GAGCCCCACT GGAACTCGGA GCACGTCCCA GAGTGGGCTC TCTCGCGAAC ATGCAAGGCT 660 GGGCACAGCA GCTGTGACAT CCCAGTCCCC ACCTCCTTGC CTGATAACCG CCTCACACGC 720 CTGCCTGGTG GGTTCTTTCC TTATATAGCA GTCACAGAGA CCGCCCTTCC TCACCCCGAC 780 AAAGGAGGTA GCCTCGTGTT TGAACTGGGA TTTATCTTTA ATAAAAACCG TAGAAGCCCA 840 AACTCAGGCG GACTGGGACC CGCCTACCAT GACTCGGCAG TGTTTTGGGG TTTGGGCCAA 900 GTAACTGGAA GAAAACCTCT TAACATGTGA CCATGTTTAC AGGCTCCGGG GAGTTCAGCC 960 TAAACACCAT GTGACCAGAG CACAGAGCCT AGGTGCAAGC CCAAGGGAAC CTTGTCACCG 1020 GGTGACAAAG AGTGAGTCAG GGGGCCCGGT GTGGCTCAGC AGGGAGGGAG AAATTCCCCG 1080 GCTTGTGGGG AACAGATGCC TCACCGGGCG TCGGCCTCCT GCCCGTCCCT GGATTCCTTA 1140 AGGAGAAAAA GAAAGCACCC ATTGTGCGGG GTGAATGCCC CAGTATCTTC CAACCAAGTG 1200 GGGAGGCACC TCCTGGGCAC GGAGTTGGCT CAGCCTGGCA GCCCCGGCCG CACGGGGCAC 1260 AGAGACCCAC AAGCAGCTAC TTGTCCCGGC TCACACAAGG GGCCCTTCTT CAAGGTTAAA 1320 AGTATCGCCC AGAGACATGT AGTCACCAGA GCCCCAGCTT GGACTCAGGT GCGCCCCTAG 1380 GATTCCAGGC TCTGTGCGCT TCCCCCGCGA ATAGCTGGGC TCCCGTACCG GCGAGGTTCA 1440 ACCCCAGAGA GCCTGCCCAG CCCCTGGCCC 1470
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