Tag | Content |
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EnhancerAtlas ID | HS047-33875 |
Organism | Homo sapiens |
Tissue/cell | Fetal_placenta |
Coordinate | chr9:33138850-33140310 |
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) |
BCL6B | MA0731.1 | chr9:33139223-33139240 | TGCCTTCCAGGAGTTCC | + | 6.02 | NFYB | MA0502.1 | chr9:33140242-33140257 | CTGATTGGCCAGTGG | - | 6 | RREB1 | MA0073.1 | chr9:33138936-33138956 | CCCCAACACACACACTAACG | + | 6.46 | ZNF263 | MA0528.1 | chr9:33139345-33139366 | CTCTTCTCACTCTCCTGCTCC | - | 6.41 |
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| Number of super-enhancer constituents: 34 | ID | Coordinate | Tissue/cell |
SE_00330 | chr9:33138866-33141700 | Adipose_Nuclei | SE_00992 | chr9:33138818-33140399 | 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_18081 | chr9:33140148-33141844 | CD4p_CD25-_CD45ROp_Memory | SE_18665 | chr9:33135758-33139718 | CD4p_CD25-_Il17-_PMAstim_Th | SE_18665 | chr9:33140056-33142210 | CD4p_CD25-_Il17-_PMAstim_Th | SE_20045 | chr9:33134255-33146063 | CD56 | SE_22416 | chr9:33135220-33146719 | CD8_primiary | SE_26031 | chr9:33139672-33141321 | Duodenum_Smooth_Muscle | SE_26859 | chr9:33139260-33140484 | Esophagus | SE_27770 | chr9:33139911-33141110 | Fetal_Intestine | SE_29800 | chr9:33139312-33141840 | Fetal_Muscle | SE_31534 | chr9:33139337-33140430 | Gastric | SE_32659 | chr9:33135226-33145795 | GM12878 | SE_40894 | chr9:33138811-33142004 | Left_Ventricle | SE_41831 | chr9:33139282-33140314 | LNCaP | SE_42236 | chr9:33137933-33140413 | Lung | SE_44340 | chr9:33139198-33141245 | NHDF-Ad | SE_45447 | chr9:33139306-33141157 | NHLF | SE_45731 | chr9:33138938-33141879 | Osteoblasts | SE_46917 | chr9:33138775-33140378 | Ovary | SE_47814 | chr9:33139478-33140178 | Pancreas | SE_48426 | chr9:33138706-33140393 | Psoas_Muscle | SE_48738 | chr9:33136686-33140472 | Right_Atrium | SE_50176 | chr9:33134918-33140478 | Sigmoid_Colon | SE_51651 | chr9:33138989-33141643 | Skeletal_Muscle | SE_52621 | chr9:33139293-33140398 | Small_Intestine | SE_53402 | chr9:33139080-33142103 | Spleen | SE_58985 | chr9:33124740-33168862 | Ly3 | SE_62118 | chr9:33106994-33169093 | Toledo | SE_62346 | chr9:33106942-33169226 | Tonsil |
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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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| Number: 1 | ID | Chromosome | Start | End |
GH09I033133 | chr9 | 33133697 | 33146567 |
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Enhancer Sequence | CCCTCAGCAA CTGACACCAC CATCTCCCCA GGGCAGAAGC TGATACCCGG GTGGTCCATC 60 TTCTATTCCC CCTCCTCTCT CCCCAACCCC AACACACACA CTAACGCTCT CTCACCCTCA 120 CATACACACA CACACACGCC CACTCGCTCC CATGCCGGGG CTGTCCACAG CATGCTGACA 180 ACCCACAGAA GCCGATCGAG CACCAAGCCA GAGAGTCTTT ACTCTGAAAT GTCTGTTAAC 240 TGCAAACTTG CCCTGTGATA TGTATCAAGA CCACTTTCAA TTTGTTTCAA TTGATACTTT 300 CTGGGTACCT ACTGTGTGCC AGCCCAAGGA GGAGTGGGTT GAGGTAGGGA GGGAGGATGG 360 ACAAGACAAA TCCTGCCTTC CAGGAGTTCC CTGCTGAGCG TGTGGCAGAA CCTAAATGAA 420 AATTACCCTG GTTTAAGGAT GGTCAAGGAG CTTGCTCCTC CAATGGCTCT GTGCAGAGCT 480 TTATCACTGA ACAGCCTCTT CTCACTCTCC TGCTCCCTTC TGAACTCGCT GTGCCCCTTG 540 CACAACCCCC ATCATGCTTC CAACACACTG AGACACCTTG ACCCCCAATC CTGCCCTTCT 600 TGCCAATCTG GCAATTTTTT CTCCACAACT CTAAGGATCT TGCAGCTCAC ACCTTTGAGA 660 CAACAGACAG CAGCCCCAGA CCTGGCGTTG AATGACTAAT TGGGTCGAGT GCCAGCCAGG 720 AGGCCTCCTG AATGCCCTGC ACACCTCCTG CCATACTGCA GGGACCATGC TCTGCTACAC 780 ACCTGGCTCT GTCCCAGTGA GAAACTCCAG AGAGCTCAGA CTCCAGGAAG GCAACGACTA 840 CCTCTGTTCA GAATCATGCA GACCTGCGAC CAGGTTTCAG AGCCACTGCC TGGGGTGGTG 900 GGGAGAAGCT CTGGGAGGAG GCAGAGGGCT GAGGGCTTCA TGACAGGCCT CAAGCCGAGC 960 CAAGGCGCCC TTGCTGTGCG GCGCATGGCG TGTGCTACCA CAGGCTCTCG GCCCCGCTGG 1020 GCTGGCTTGT GTGTTTTCTT GGCTCTGGAA GCTGGGAGGC AGGGTTACGT AAGCAGATGA 1080 GCAGATGTAA GCTGTCCTCG GCTCCCCCAG CTCAAGCCCC GCCACGTGGG CCTCTCGGCT 1140 GGGAGTCCAG GTCATGGCCT TGCATGTAAG TCGCTCAATA ACTTCAATGT GTGAGCTCAA 1200 TTCAGACAAA TTCCACTGCT CCCCTGCCTG GCACAGCAAA CCCAAACACA TACATGCCCC 1260 TCCATCAAAG GCCCTGCTAA TCTAAGCCAA CACCAGCACG GACTCCTGAC TGGTTTTCAT 1320 GCTGGCTGAA GCACTAGTTC AATCCTTTAG CCTCAGCAAA ATAGGCTGAA ACATCTAGTC 1380 ACTGTTTGTC AACTGATTGG CCAGTGGGTC GAAAGAAGCG TTGGCCTGAT GCTTTATTGT 1440 GACAATGTTT CACTAGCCCA 1460
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