Tag | Content |
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EnhancerAtlas ID | HS092-01358 |
Organism | Homo sapiens |
Tissue/cell | HFF |
Coordinate | chr1:43397480-43399200 |
Target genes | Number: 17 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
MYB | MA0100.3 | chr1:43398565-43398575 | GACAGTTGGT | - | 6.02 | RREB1 | MA0073.1 | chr1:43398223-43398243 | ACCCAACCCATCCCAACACC | + | 6.09 | SREBF1 | MA0595.1 | chr1:43398835-43398845 | ATCACCCCAC | + | 6.02 |
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| Number of super-enhancer constituents: 41 | ID | Coordinate | Tissue/cell |
SE_01795 | chr1:43397398-43398157 | Aorta | SE_05390 | chr1:43397289-43399585 | Brain_Cingulate_Gyrus | SE_06192 | chr1:43395065-43405505 | Brain_Hippocampus_Middle | SE_07319 | chr1:43396705-43398566 | Brain_Hippocampus_Middle_150 | SE_08269 | chr1:43397488-43399602 | Brain_Inferior_Temporal_Lobe | SE_10377 | chr1:43396392-43405534 | CD19_Primary | SE_11009 | chr1:43387831-43425728 | CD20 | SE_12470 | chr1:43397348-43399808 | CD3 | SE_13825 | chr1:43396778-43399313 | CD34_Primary_RO01536 | SE_14471 | chr1:43395753-43414527 | CD4_Memory_Primary_7pool | SE_19657 | chr1:43396427-43405202 | CD4p_CD25-_Il17p_PMAstim_Th17 | SE_20345 | chr1:43395492-43405550 | CD56 | SE_20799 | chr1:43396312-43405729 | CD8_Memory_7pool | SE_22754 | chr1:43395674-43405513 | CD8_primiary | SE_23189 | chr1:43397346-43399720 | Colon_Crypt_1 | SE_23904 | chr1:43397399-43399265 | Colon_Crypt_2 | SE_25177 | chr1:43396926-43398787 | Colon_Crypt_3 | SE_26580 | chr1:43395721-43413249 | Esophagus | SE_29267 | chr1:43397108-43398616 | Fetal_Intestine_Large | SE_31882 | chr1:43396701-43399114 | Gastric | SE_33837 | chr1:43396695-43400408 | HCC1954 | SE_34353 | chr1:43395339-43412997 | HCT-116 | SE_36013 | chr1:43398145-43399517 | HMEC | SE_37191 | chr1:43393285-43398371 | HSMMtube | SE_39883 | chr1:43397369-43405479 | K562 | SE_41620 | chr1:43397520-43399349 | LNCaP | SE_42796 | chr1:43396336-43399368 | Lung | SE_50202 | chr1:43396219-43406255 | Sigmoid_Colon | SE_54088 | chr1:43396020-43399837 | Spleen | SE_55340 | chr1:43396132-43399459 | Thymus | SE_55821 | chr1:43396763-43399673 | u87 | SE_57045 | chr1:43396858-43405413 | VACO_400 | SE_57417 | chr1:43397518-43398729 | VACO_503 | SE_58269 | chr1:43397518-43398137 | VACO_9m | SE_58561 | chr1:43388242-43430420 | Ly1 | SE_60624 | chr1:43388552-43428820 | DHL6 | SE_62392 | chr1:43388423-43425814 | Tonsil | SE_64094 | chr1:43397486-43398043 | HSMM | SE_64340 | chr1:43397259-43405516 | NHEK | SE_67781 | chr1:43396763-43399673 | u87 | SE_68708 | chr1:43393050-43401454 | H9 |
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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 |
GH01I042929 | chr1 | 43395541 | 43414526 |
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Enhancer Sequence | AGTGAGACTC TATGTCTCAA AAAAAAAAAA AAAAAAAGAG AAATACAGAA GGAAAAGGGT 60 CTTCCCACTT GCCCCTTTTC TCCTCACCAT GTCTCAAAGC CCCAGGGGCC CATCTCCTGC 120 CATCAGGCCC TCCCCCCAAC CCCTTGCTGG GGAGGAAGCA GGGCTTGACA GACAGGTTCC 180 GCCATCCAGG AAGTACAGAC TCCCTGACCG CACTGAGGGC CTGGTGTGAC AAACTCACAC 240 ATGTCACCCT TCAGAAGTGC TTGAAAGACT CACGCTGTGG CTTTCTGTTC CCCAGGCCTA 300 GCTCCCTTGT GTCTGGCCTG CGAGCACCCC CTTGAAGGAC CCACGGCCTC CTCCCCTCTC 360 CCAAGGGCCC AGCTAGGAGG TATGGGGAAA GGTTCCACAC AAGGAAGCAG TTCCAGGAAC 420 TGGAAACGCC CGTCCTAGGG CAGCCCTGCC CACCAGCCCT GCCCCCACCC TGGCCAGCTC 480 CCACGGATGT GGTAGGCAGG CAGCACCCGT TCTGCCTGAG CACACTCACC ACACTCTCAG 540 TGCCATGGGA CTGGCCAGAC CCACCCAGCC ACACGTATAG CAGAGTGCAG GCCCTAGTTA 600 CCCAGAAACG GCTTCTTATG CACGTATACC ATCACACACA CATACCCGTG CTCATAGAAT 660 CTAAATATTC CTGCTTTAGC CAGTCACAAA CTCACATGCC CCTCATCCCC TACCACTTAC 720 AGCTCAAACT CAATTCCATG TGAACCCAAC CCATCCCAAC ACCCCTCCGT GTGTGTGCAT 780 GCCACAGGTT CATGCACACA CAGCGGTATG CAGCCTCTGC AGCCTCCATC ACTGCTGTTG 840 GTCCTCCCTA TCCCTTCCAA CCCACTGAGG TCTAGCAGAA GAAGAAGGTG TGGGCAGGCA 900 CACTTGCCAA ACCAAAGCCT GCAGTCCCAG AAATGCCCAC CTATTCAAAT ATGCTGGGCC 960 TGCCTCCTGG TGCCTTCCTT CCCATTGCTG TGGGTGCTCA GCCTCTAGCC ATCTTTTCCC 1020 CTGCCCTGTC ACAACCTGTC CCAAGTCAGC AGGCATCTGA TGGAGGCCAG GCTCCAAGGG 1080 GCGAGGACAG TTGGTAGGGC AGAGGCAAGC CCTAAGGATC TGCTTGTCCG TTCCAAGGAC 1140 GCCATGCAGG GCAGTGAATA GAAACCTGAA CTCTGATTCT GGACACAACT AAATTCAGGT 1200 CCTAGCTCCA CCCCTTATTT CCAGTGTGAC CATGAGCAAG TTATTTCATC TGTGAGTTTC 1260 CATGGCCCCA TTTCTAAAGT GCAGACATTA GCAGGAGCTG CTTCACAGTG CTGCAGGGAA 1320 TCAGTGAAAC AGTGCTTGGT GTCATCATCC CTAAAATCAC CCCACTGCAC ACTGGTGGCC 1380 TGAAGGCTGT GCAGACCACT AACAGAGTCT CCCCAAGCCT TCAACCCGTA ACTCAAAATC 1440 GGGGCTCCTG CCAGGTATCA ATCCAATCTC CCTACCTACC ACACCTTTGC ACTCACTACA 1500 CACCATCTCC CACCCCTCTA CGCCTTTGAG ATGCTACTAC TCCTGCCTGG AAGGTACCCC 1560 TGGCCTTATT GCTGAAACCT TTCGAGATCC AGGTTTCCCT GACTCCAGGA GTTTGTCTTC 1620 CCTGAGGAAG ACAGTTGATT CACACCATGG TCTGTCCCAG AGCCAGTGCC AGGGATACCT 1680 GGTGAGGAAA TGGAGGAATC GAACCAAAGG TGTTAGGCTC 1720
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