Tag | Content |
---|
EnhancerAtlas ID | HS046-00350 |
Organism | Homo sapiens |
Tissue/cell | Fetal_muscle_leg |
Coordinate | chr1:17239400-17242400 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Hnf4a | MA0114.3 | chr1:17239982-17239998 | GAGGTCCAAGTCCAGT | + | 6.07 | KLF5 | MA0599.1 | chr1:17240495-17240505 | GCCCCGCCCC | + | 6.02 |
|
| Number of super-enhancer constituents: 67 | ID | Coordinate | Tissue/cell |
SE_01476 | chr1:17239966-17242069 | Adrenal_Gland | SE_02875 | chr1:17240618-17241434 | Astrocytes | SE_03430 | chr1:17238100-17239778 | Brain_Angular_Gyrus | SE_03430 | chr1:17239783-17240499 | Brain_Angular_Gyrus | SE_03430 | chr1:17240731-17242488 | Brain_Angular_Gyrus | SE_04111 | chr1:17237927-17240527 | Brain_Anterior_Caudate | SE_04111 | chr1:17240628-17242448 | Brain_Anterior_Caudate | SE_05172 | chr1:17237770-17246094 | Brain_Cingulate_Gyrus | SE_06210 | chr1:17237645-17245771 | Brain_Hippocampus_Middle | SE_07232 | chr1:17238080-17242647 | Brain_Hippocampus_Middle_150 | SE_08076 | chr1:17237896-17246252 | Brain_Inferior_Temporal_Lobe | SE_08889 | chr1:17239947-17240454 | Brain_Mid_Frontal_Lobe | SE_08889 | chr1:17240789-17242026 | Brain_Mid_Frontal_Lobe | SE_10448 | chr1:17239853-17240476 | CD19_Primary | SE_11024 | chr1:17237883-17245307 | CD20 | SE_12131 | chr1:17240859-17241779 | CD3 | SE_13570 | chr1:17240617-17241484 | CD34_Primary_RO01536 | SE_14531 | chr1:17239563-17241985 | CD4_Memory_Primary_7pool | SE_15440 | chr1:17239829-17241939 | CD4_Memory_Primary_8pool | SE_15839 | chr1:17240568-17241687 | CD4_Naive_Primary_7pool | SE_16401 | chr1:17239578-17241745 | CD4_Naive_Primary_8pool | SE_17223 | chr1:17239936-17240632 | CD4p_CD225int_CD127p_Tmem | SE_17223 | chr1:17240641-17241519 | CD4p_CD225int_CD127p_Tmem | SE_17702 | chr1:17238954-17242280 | CD4p_CD25-_CD45RAp_Naive | SE_18224 | chr1:17239283-17242338 | CD4p_CD25-_CD45ROp_Memory | SE_19865 | chr1:17239824-17242024 | CD4p_CD25-_Il17p_PMAstim_Th17 | SE_20182 | chr1:17239788-17241910 | CD56 | SE_20877 | chr1:17239477-17241855 | CD8_Memory_7pool | SE_21501 | chr1:17239632-17241900 | CD8_Naive_7pool | SE_22012 | chr1:17239593-17241877 | CD8_Naive_8pool | SE_22656 | chr1:17239909-17240454 | CD8_primiary | SE_22656 | chr1:17240604-17241913 | CD8_primiary | SE_23911 | chr1:17239885-17240478 | Colon_Crypt_2 | SE_23911 | chr1:17240479-17241564 | Colon_Crypt_2 | SE_25305 | chr1:17239947-17241454 | Colon_Crypt_3 | SE_27153 | chr1:17239835-17242028 | Esophagus | SE_28353 | chr1:17239867-17240494 | Fetal_Intestine | SE_28353 | chr1:17240610-17241704 | Fetal_Intestine | SE_29508 | chr1:17239703-17240542 | Fetal_Intestine_Large | SE_29649 | chr1:17238840-17240515 | Fetal_Muscle | SE_29649 | chr1:17240656-17242112 | Fetal_Muscle | SE_31118 | chr1:17238627-17240491 | Fetal_Thymus | SE_31118 | chr1:17240712-17241947 | Fetal_Thymus | SE_31881 | chr1:17239819-17242135 | Gastric | SE_33013 | chr1:17239950-17240437 | H1 | SE_33013 | chr1:17240620-17241403 | H1 | SE_33540 | chr1:17239257-17245174 | H2171 | SE_35172 | chr1:17239807-17241711 | HeLa | SE_42843 | chr1:17239864-17243201 | Lung | SE_45444 | chr1:17239949-17240367 | NHLF | SE_47744 | chr1:17239961-17240545 | Pancreas | SE_47744 | chr1:17240549-17242006 | Pancreas | SE_51608 | chr1:17238813-17242145 | Skeletal_Muscle | SE_53155 | chr1:17238762-17240528 | Small_Intestine | SE_53155 | chr1:17240572-17241791 | Small_Intestine | SE_53544 | chr1:17238838-17241941 | Spleen | SE_54964 | chr1:17238808-17242458 | Stomach_Smooth_Muscle | SE_55554 | chr1:17240073-17240473 | Thymus | SE_55554 | chr1:17240575-17241458 | Thymus | SE_61917 | chr1:17221528-17256732 | Toledo | SE_63124 | chr1:17215209-17241689 | Tonsil | SE_63250 | chr1:17222916-17254487 | GLC16 | SE_63321 | chr1:17222804-17249569 | NCI-H82 | SE_65449 | chr1:17237943-17242529 | Pancreatic_islets | SE_67642 | chr1:17239816-17240437 | u87 | SE_67642 | chr1:17240556-17241577 | u87 | SE_68996 | chr1:17239943-17241712 | H9 |
|
| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr1 | 17239897 | 17240265 | chr1 | 17239430 | 17239585 |
|
| Number: 1 | ID | Chromosome | Start | End |
GH01I016912 | chr1 | 17238896 | 17241927 |
|
Enhancer Sequence | TTTCAGAGCC CGAAGGGCAC ACTGGCAGCC TTTAGTGCAG TGTTTCAGAT GTCACAGACA 60 GGTTCCTCTT TGACGAAGAT GGAACTTCCA CTGCTTCCCT CCTACCACGC AGGAAACACA 120 GAAGCAACCA TCAGCCGAGG GCCTGCTGGC CGTTCTCTCT GGGTACTGTG TTTGGAAAAA 180 GCACAAAATC ATTAACTTAA ACATGCTTTT TCAAACCAAA CACATCCCTC TCTTAGCCCT 240 GGAGATTCAG AGCTGCCTCT CCCTTTGAAA ATGAATGATC TCGCCCGGGT GCAGTGGCTC 300 ACGCCTGTAC TCCCAGTACT TTGGGAAGCT GAGGCGGGTG GATCGCGAGG TCAGCAGTTT 360 GAGACCAGCC TGGCCAATAT GGTGAAACCC CGTCTCTACT GAAAATACAA AAATTAGCCG 420 AGCGTGGCGG CGGGCGCCTG TAGTCCAAGC TACTCAGGAG GCTGGGGCAG AGGTTGCGTT 480 TAGCCAAGAT CATGCCACTG CACTCCAGCC TGGGCAATAG AGCAAGACTC CCTCAAAAAA 540 AAAAAAAAGC ATGATTTCAT CCAATGCCTT CAATAACAGA AGGAGGTCCA AGTCCAGTGA 600 GAGGGTGGAA CGAACATACT GTCACAGTGG AAAGGACACG AGACAGGCGC GCCACCGGGT 660 TGAGTCTCGC GAACAAACTG AGGCCAGAGT GCCTTCCCCA GGGCTGCACG TCAGTCAGGA 720 AAAAAAAAAG CATTCTCTCC GACAGGTCAA ATCACCGAAG CCTCGGGATC GTCGCTGGGG 780 GCTGTGACGG GGCTGGCATG AAACGTCCCT CTGTCTGGCT GGGCGATGGG TCAGTGCTCA 840 GGAGTTTCAG GCCTTTAAGG CCCGGCCAGA CCGCAGGGGG ACTCTGCAGC CGGGTCGGGG 900 TTTCGATCCT GCGCTGCGGC CTTGCAACTG CGAGGACTTG GGGGTCGTGC TTCGTTCGCC 960 TGGTATCCTC GTTCGTGCGT GTAGGAGGCG CCTGGCTTGC CGGGCGGTGC CAGGCGGCAA 1020 GAGGGAGGGC GCACGGAGCG TGTCCGCCCA GGGCGGCCCC TGTAAGCGCT GCAGAAGCGC 1080 TGCTCCCGGC GCCCGGCCCC GCCCCAGCCT CCGCCCCACT ACCGCGCAGC GCAGGCTCCG 1140 CCCCCAGTTT TCCCCGCCCC GTGGCGGGGA CGCCCCGCCC GGTCCGGCCC GCTCGGCCTC 1200 GGCAGCAGCG GCTGCGGCGA AGGCGCGCGA AGGTAGGTGG CCGGGGGCGC GCGCGTGCGC 1260 GGGGGCGGGA CGGACGCGCT CCCGGCGGAG GAGGCCGCGC GCCTGGGGGC GGGCTGGAGC 1320 CACGTACCGG GGCTGGGGGC GCTGTGTGTT CCGCGACTGC CGCGGCCCGG CACCGGAGGC 1380 CAGGAGAGCG TTCCCAACAG GCTCCGCGGA TGCCCCGCCG CGTCCTGCCG CCCATCCTGC 1440 CCGGATTGTC GCGGGCCGGG GGCACGACAG GAGACTGGGG CCTGCAGGGC GCAGCCGTCC 1500 CTCCGCCGGC CGGGGTCCCC TCGCTCCGCG GGCGGCCGTG GGAGGCCCTC GCGACGGCCT 1560 CTGCCCCCCG CAGATGCCCT CTGCAGCTCC TGCGTGCGGG CCCCGCCCTG CACTGCCCTC 1620 CTCGTGTGGG ATCCGGTTTC GTCTTCATTG CAGCCCTGCC GAGTCGGAAG CATCTCCATT 1680 GTGCGGATGG GGAAACTGAG GCCCAGAGCG CATAGTTGGG CTGGCCACGG AGGCAGGGCC 1740 GCCGGATGCT GTGCGGGGAT GGGGCCCTGC ACCCCTTGCG CCTCTCACCA TGCGGCCTCA 1800 GGCCTCTGTG CCCGGCAGCG TCTCTGGAGT GGGCATTTTG AACGAGCTCC CTCCTGATTT 1860 TCACACAGAC TTAAGCCTGA CGACCATGCT GGGGCGGATG TCTGCCCCTC TGGTGACCAG 1920 GTCACAGCTC CCTTGGGAAG ACGATTGACT GGGGAATGGG GACCCTGGGG AGGAGGACTT 1980 CAGGGTGCCA TCTGTCTGTT TACGCCAGAA AACAGAGATT TCTGTTTTCT TTCGCTGGGC 2040 TCACAGCAGG TGCTTAATAA ACAGATCTTG TGGCGGGAGC AGACGACAGC GAGGTTCAGG 2100 CAAGACTCCA GGAGTCAACC CCTGGATCTC GGAGGCTCCC CACCCGCGCA CATTTCCCTG 2160 ACTTAACCCT CCCCTCCCCA AGTCTTTCAG CCCTTTCCAC CCAAGTGGCC CCTGTGGGGG 2220 TCACTGCCTG GTTTTCACCC TGATCTTCTG GGATGCGGCA GATGCTGGCT GGATATGTGT 2280 TCGCTGGTGT CCTTCCGTGA TCCCCGTCTG TGGCTGACAC CATCTGTGGC CCAACATGAC 2340 CCCAGCCAGA GCCAAGGGGA ATCATTTCTT TTTCCATTTA ACATCCTATG TTATTACTTG 2400 GCTCTTAGCA TTCATTAATT CATTCAGCAG CTCTTCATGG AGCTTTGGCC TTAGCCCATG 2460 CACTGTGGAA GTGACAGTGA GCTAAGCCAA CCTGGCACTT TGGGAGGCTG AGGTGGGAGG 2520 ACCGCTTGAG CCCAGGAGTT GGAGACTAGC CTGGGCAACA TCTCATCTCT ACAACAAGTA 2580 AAAAATTAGC CAGACGTGGT GGCACGCACC TGTGGTCCCA GCTACTCAGG AGGCTGAGGT 2640 GGGAGGATCC CTTAAGCCCA GGAGGTCAAC GCTGCAGTGA GCCATGATTT TGCCACTGCA 2700 CTCCAGCCTG GAAAACAGAG CAAGACCTTG TCTCAAAGAA AAAAAAAAAA AAGGAGGAGA 2760 CAGACAACAT ACATGTTGGA GAAAATGGAA CAGCCACTGG AGGGACCTCT TTAGCTGAGA 2820 GTCGGGGTAG CTCCCTCAGA AAGTGATATT TTTGAGCCAA AATCTGGCCG ACAAGCGGGA 2880 GTCAGCTGTG CAAAAGAAGG GGGAAGTGCG TCCCAGGCAG AGAAAGTGGC AGTGCAAAGG 2940 CCCAGAGGTG GGTGCCTGCC TGGTGTTTGA GGAATCAAGA AGGCCATGAG CAGCCAGGTG 3000
|