Tag | Content |
---|
EnhancerAtlas ID | HS017-32941 |
Organism | Homo sapiens |
Tissue/cell | CD14+_monocyte |
Coordinate | chr9:33135420-33138340 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ESR2 | MA0258.2 | chr9:33137832-33137847 | AGGTCAGCCAGGCCT | + | 6.25 | Zfx | MA0146.2 | chr9:33137840-33137854 | CAGGCCTGGGCTGC | - | 6.2 |
|
| Number of super-enhancer constituents: 30 | ID | Coordinate | Tissue/cell |
SE_00330 | chr9:33134396-33136684 | Adipose_Nuclei | SE_00992 | chr9:33134966-33138299 | Adrenal_Gland | SE_09459 | chr9:33134458-33139068 | CD14 | SE_10229 | chr9:33134720-33146706 | CD19_Primary | SE_10912 | chr9:33119344-33169982 | CD20 | SE_12090 | chr9:33136393-33139356 | CD3 | SE_14891 | chr9:33136466-33138896 | CD4_Memory_Primary_7pool | SE_18665 | chr9:33135758-33139718 | CD4p_CD25-_Il17-_PMAstim_Th | SE_19329 | chr9:33136605-33138149 | CD4p_CD25-_Il17p_PMAstim_Th17 | SE_20045 | chr9:33134255-33146063 | CD56 | SE_22416 | chr9:33135220-33146719 | CD8_primiary | SE_26859 | chr9:33135768-33137338 | Esophagus | SE_27770 | chr9:33133434-33136209 | Fetal_Intestine | SE_28724 | chr9:33133427-33136185 | Fetal_Intestine_Large | SE_29800 | chr9:33134401-33137058 | Fetal_Muscle | SE_31534 | chr9:33135301-33136542 | Gastric | SE_32659 | chr9:33135226-33145795 | GM12878 | SE_40894 | chr9:33134620-33138311 | Left_Ventricle | SE_42236 | chr9:33134930-33137913 | Lung | SE_42236 | chr9:33137933-33140413 | Lung | SE_46917 | chr9:33134890-33136451 | Ovary | SE_46917 | chr9:33136917-33137295 | Ovary | SE_48738 | chr9:33135011-33135823 | Right_Atrium | SE_48738 | chr9:33136686-33140472 | Right_Atrium | SE_50176 | chr9:33134918-33140478 | Sigmoid_Colon | SE_51651 | chr9:33134813-33136290 | Skeletal_Muscle | SE_53402 | chr9:33134893-33138878 | Spleen | SE_58985 | chr9:33124740-33168862 | Ly3 | SE_62118 | chr9:33106994-33169093 | Toledo | SE_62346 | chr9:33106942-33169226 | Tonsil |
|
| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 3 | Chromosome | Start | End |
chr9 | 33135712 | 33136351 | chr9 | 33136531 | 33137040 | chr9 | 33137041 | 33137549 |
|
| Number: 1 | ID | Chromosome | Start | End |
GH09I033133 | chr9 | 33133697 | 33146567 |
|
Enhancer Sequence | CACTAGAGAG GTGGAGGGAG GGAGAAGTTA GCAGGCCACA GGACTCGCCA CCGCTCCACA 60 GGCTGCATCA GATGGCCAGG CTGCAGCTGC AGCTGCAGAG GAAATGTCTC CTCCTGGGAG 120 GCAACGTGGC CACGGAGAGG GCCCTCCTGC CCAGCATCAG GCACCACATC CAGCATTAGG 180 GTGACCAACC ATCCCCAGAA ACCCCCTTCA GTGTGGGGCA AACCTAGATG GTTGGTCACT 240 CTGTGAAGCA CTCGCCTGCC CAGGACCCTC CCCGCTCTGA CTCCACTGTA AAATGGAAGT 300 AATTTCTACC CAGACTTCCT GACAGGCTGT TGTAGAAATC AGTGATCACG GATGAGAAGG 360 CAATTTCTCA AAACCCCTGA GGTTGAGACT TAGCTCTGTG ACCTCCCAGC TGCGTGGCCT 420 TGGACAAATG GCTGACATCA TCTCTCTGAT TCTAGCCTAA CTGGGGAAGT GTGTGTGTGT 480 GTGTGTGTAT GTGTGTGTGT GTGTGTGTGT GTGTATGCAT GCATGTTGGG GACGTCAGTG 540 TGGAGGGAGT TAGCTTCGAA GTGGAAGGTA GCAGGAGTGG CATGAGTGCC CATGTCCCAG 600 GAAGGGACTC GATGGAAGGT GAACCAAGGT CTGGGAGAGA TGGAGGCAAA GAAACCCCAA 660 AGGAGACCGA GGGAAAATAA AAGAAATAGC TGGAAACACA GAAGAATGTT TAGTAACAGA 720 GGGGATAAAG TAACAAAGAG GAAGAAGAAG TAACAAAGAG GGAGGGATGA CTCCCAAGTT 780 TCTGGCCTAG AAGAACATGG ATGCAGATGA GATAAGTAAG TTAGTAAGAG AGTGCTTGCC 840 TCAGAAGAAA AATGGATGAG GTGCAGATTG TGGATTGTGA GGTAACGGCA GGTGGGAAGA 900 GGGATGAGGA AAACGTCACA TACCGGGTAT GTGGTACACG TGGTGCAGTC CAGGCAACAC 960 AGGGAATCAA GGCTCTGCTG AGAGTCAAGA GCCAAGGCTT GAACCCAGGC TCCCCATACT 1020 CTCTGCAGAC CAGACCGCCT CAAAATGGGT TCCAGAAAAC ATCAGACCCA GCAAGATGCT 1080 TAATGGAAAA ACATGTCTCG TGGTCAAATA AGAACGGGAA TGCTGCGTAT TAAATCCTGC 1140 TTCTGCAAAG TCACGACACA CACCAAAGGC TCTGAGAAGT TGTGCAGTCG AAAAACCCCC 1200 TTCGTTATAT TTAACCCACC ATTTCCCAAG CTTATTTGGC TACAGAACCA TTTTTCCAGG 1260 GAACACACTT TGGGAACTGT TACTCTAGTG TAACCAGCTT CACCTGTGAA GCAAATGAGC 1320 CACAAGAACA AAGGAAGGAA CCTAGAGAAC AGGTAGGAAC ACCAACCACA AGCACAGATC 1380 AAAACCTGAA ACATGCTGGT GAGAACCCGC CCAGGGCCAG TGAGCAGGCT TCAGCCTGCC 1440 CTGTTTATCA ATAACGCGTG GCTCTCCAAG CACCCCCTAC TCCCGGAATC ACTCGCCCTT 1500 CTGAATTCAA CAGCTTGAGA AAAAAAGCTG TGGGCCTGCT TCCTCTCACC AGATAGCTGC 1560 CACTTCCACC CCCTTCCCCA GTACACATCT CACATCTTCC CTCCCTCCGT AGCTGACCCA 1620 GGTCCACCAT CACAGGACCT GTTCCCATTA GTTTGTTTTC TTCTGAGATA CAGCCCCGAC 1680 CATATTACTT TCCCACTAAA ACCTCCAGTG GCTCTAAGGC TGTGTGTCCC TGCACAAGGG 1740 AAGGCCAAGG CCCACAGCTG AGCAAAAGGC CCTTCACCCT CAGCTCTGTC TGTCTCCCTC 1800 CCCATCCCTT AAGCCATGCC TGTCCACACT TTTCTCTTTG CCAGAAATGC CCTTCCCACT 1860 CTCCTCTTAA CTAGCAAACT TTCGCATTGA GAGATAGGCC TCAATCAAGC TTGATCCTTT 1920 TACTCTCTGC GCTATCACAG AGCTCAGGCA GCAGACCCTC TGGGGCAGGG AAGAAGATCC 1980 TCAGGCCTCC CTCTCTGGTC ATGCACCTCC CTCCTGGAGG GACAGAGGCC TTGAAGCTCA 2040 GTCCCTTATA AGACTGCCTG CTGAGCCAGC TCCCACCTCC CAGGGTGCCC TAAAGTGAGC 2100 AGGCACTGTG CTCTTCAGAG AAGACCAGGA CTCAGTCAGT GGTCACCCTG GACAAGTTTT 2160 TCCCAAACCT ATCACAAGAA TTGCTTGAGG AAGTTAGTAC AAGTACAGCA TCTCGGGCCC 2220 TTCCCTTAGA GAGTCTGTGG ATTTTGGGAA GGACCTAAAT GGCTACCTAA CAAGGAGCCC 2280 AGATGATTCT CACTGGGCAA GCTGGGTAGT AGGGCTCCGA TGGACCATCT GATGGGCATC 2340 TGATGTCAAG GCTTAGGGCT TTCGGGCAAA GAGGGCCCTC GGGGATTCCC ACCATTCACA 2400 CCCTTCCCCA CAAGGTCAGC CAGGCCTGGG CTGCCCAACA CCCAACCCTG GGCAAAGGCT 2460 ACTGGGGGGG CCCTGCTGCA CAGTGAACTT GTGAAAAACA TGAAGAAAAG ATCTGTCACA 2520 GGGCTCTTTT CACTTCAGAG GGCCCCCACA ACATCTGCAG CCCCCACCCC ACCTTTGGTT 2580 CTGAGGATGC TGCTAAACAT AACCGCGTTT TGGGGAACCC AAGAAGCACC TGGGCTGTCA 2640 CCCTGCCGAC TTGCTCGTAC CTTCTGAAAC CCACCCAGAA AACAGGAATT CACATGTGGC 2700 CTGGCTCGCT TCCGCGGGAC AGACACCTGC AGGCTGGAAA GTGTCCTGGT GTTGCCCCAT 2760 CATGGGTTTC AGAAAGGTGG TCCTGAAGTC AAGAGCCCCG GACAGGAGAA GAGATGCCTG 2820 GGCCCCGGTC CAGCTCCACC AGTGACTTTC CAGATGATCT TTGGTATCCT GAGAGTGGAT 2880 AGTACAGCCA CTCTCAGGGT ACTGGTTTCC TCATTTGTAA 2920
|