Tag | Content |
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EnhancerAtlas ID | HS197-00499 |
Organism | Homo sapiens |
Tissue/cell | ZR75-30 |
Coordinate | chr1:31228130-31230500 |
Target genes | Number: 10 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chr1:31229402-31229420 | GGAAGCAGGGAAGCCAGG | + | 6.29 | FOSL2 | MA0478.1 | chr1:31229640-31229651 | CTGAGTCACCC | - | 6.02 | JUNB | MA0490.1 | chr1:31229640-31229651 | CTGAGTCACCC | - | 6.02 | Myog | MA0500.1 | chr1:31228744-31228755 | AACAGCTGCAG | + | 6.02 | Tcf12 | MA0521.1 | chr1:31228744-31228755 | AACAGCTGCAG | + | 6.62 |
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| Number of super-enhancer constituents: 32 | ID | Coordinate | Tissue/cell |
SE_09454 | chr1:31213287-31232169 | CD14 | SE_10168 | chr1:31213284-31236569 | CD19_Primary | SE_10991 | chr1:31200236-31237145 | CD20 | SE_12025 | chr1:31215434-31231414 | CD3 | SE_13126 | chr1:31225755-31231455 | CD34_Primary_RO01480 | SE_13496 | chr1:31227251-31231821 | CD34_Primary_RO01536 | SE_14586 | chr1:31213183-31237364 | CD4_Memory_Primary_7pool | SE_15642 | chr1:31225772-31231357 | CD4_Memory_Primary_8pool | SE_16057 | chr1:31225561-31231446 | CD4_Naive_Primary_7pool | SE_16511 | chr1:31225655-31231488 | CD4_Naive_Primary_8pool | SE_17022 | chr1:31225965-31231414 | CD4p_CD225int_CD127p_Tmem | SE_17372 | chr1:31209247-31236610 | CD4p_CD25-_CD45RAp_Naive | SE_17902 | chr1:31209743-31235259 | CD4p_CD25-_CD45ROp_Memory | SE_18435 | chr1:31206875-31235130 | CD4p_CD25-_Il17-_PMAstim_Th | SE_19221 | chr1:31225835-31231719 | CD4p_CD25-_Il17p_PMAstim_Th17 | SE_20090 | chr1:31213732-31235754 | CD56 | SE_20783 | chr1:31215526-31235927 | CD8_Memory_7pool | SE_21654 | chr1:31224788-31233416 | CD8_Naive_7pool | SE_22073 | chr1:31215463-31231671 | CD8_Naive_8pool | SE_22484 | chr1:31213283-31234726 | CD8_primiary | SE_31319 | chr1:31227389-31235046 | Fetal_Thymus | SE_32510 | chr1:31215436-31239752 | GM12878 | SE_43662 | chr1:31214270-31233570 | MM1S | SE_50449 | chr1:31215714-31235694 | Sigmoid_Colon | SE_53612 | chr1:31215423-31231885 | Spleen | SE_55204 | chr1:31226107-31231617 | Thymus | SE_59019 | chr1:31215557-31239184 | Ly3 | SE_60258 | chr1:31215621-31235310 | Ly4 | SE_60651 | chr1:31202709-31239413 | DHL6 | SE_61144 | chr1:31205054-31253025 | HBL1 | SE_62248 | chr1:31201545-31253778 | Tonsil | SE_67247 | chr1:31214270-31233570 | MM1S |
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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 | GAGACCATGG ATGCTGCTGA ACTTCCTCTA ACGCACAATT CACTCCCCCA AGATGAAGAA 60 TTATCCAGCC CAAAATATCA ATGGTGCACT GCAGAGAAGA TCCAACTTCT TAGCTTGTCA 120 CTCAAAACCT TTATCACCTC CTCCCCAAAC TCCAGGTTTG TCTCTATTGT GTCCCTGTAG 180 AAGCCGAACA CATACGCCAT TGCTCACCTG TTTCTCCTCA CCTTCCATAC TGCCCACAAC 240 CAAACTCTCC CTCCTGCCAA TGGCACCACC TCCAAGAAGT CTTCCATGAT TGCTAGGGCC 300 CACACATTCT TCAGCTCTGT GAGCAGGGAC CGTATATCAC ACCACCATTT ACAGGTGAGG 360 ACATCGGATG GCACGATCAA CAAGAAACCT TAACAGCCCC ACAGTCCCGG GTTTGCAGGG 420 CAGCCTCTGG GCCCACACAA CCTGCAAATG GATTTGACTT GGCCTGCACT GAGATTTTTT 480 TCTACCATGC ATCAATCACT AGCATTGAAA CATCAGAAGA TGTGACACAA AAGCCTGCTC 540 CCTATTCTCT AAACATCAGA AGAGCGGCCA CCAGGGCCCA CAATCCTTCG TGGCAACAAC 600 AAGCAAAAAC AGAGAACAGC TGCAGGGTGG GCCAAGCAAG GGCTCCCGGG GTCACCGCAG 660 GCCCCATCTG CCCCCTGCTG TCACTCACAT GGCCTGCCCA GACCCTAGAG GCATCAGAGT 720 TGGAGACCTC TGAGCCAGTC AACATCACCT TACCCCTGAC TTTATAAAAG GGAAACTGAG 780 GCCCAGAGAG AGGCTTGTCT GAGCCCATAC AGCCAGTTAG TGGCAGGGCT GGGGTGAGGA 840 CCCAGGGACT TGCTACCTGT GAGGCGCCCC TGCATGCCAC ACTGTCCTTC TAAGAATGTG 900 CATAGTCTCA GAGCTTGAAG GCCTAAAATA CAGGGTACAG GGACACTCAA AGAGTGATTT 960 GCTTCTCTCA GCTCTTGCAT TGGCAGGAGC TCGGAAGGAC AACCTCTGAG TTCCTCCTCC 1020 CAAAACTAGA GTCCTTGAAT CTGACAACTT GACTCCAAGG ATGCTGACAG CAGGTGCCAT 1080 GTCTGATGCA CAACGAATAA TAAAGCACTC ACCTGTGCGT CAGGCGTGGT TCTGCATGCT 1140 TTGTATGTAT CAACTCCCTG AGCCTCACAA CAAACCCTAT CAGATGGGTA TGATAATTCA 1200 CATCCCCATT TTTTTAAATG AGAAAACTGA GGCTCAGAGA GGTTAAGTAA ATTGCCCAAG 1260 GCTGCAGAGC TGGGAAGCAG GGAAGCCAGG ATTTGCATGC AGGAGTCTGC ATCCAGAGGC 1320 CGTGGGCTAA CCACTGAACA GCATCGCCCC CCTGAAGGCT GGGCTCTTGC CACAGCTCTG 1380 CCTGCCCTGC CTGTGACAGG AAGCAGACGC AGGCAGGTCT GAGTTTGCAG CAACCCACCG 1440 CAGCATGTGG ATCTAGGCTA ATTTTGAGGA AGCCCTTCCA GACTCATGAG AAAACTGTTA 1500 ACCACAGGCC CTGAGTCACC CCAGGAGGAA GTCGCTTGGG TCTAGGGGAG ATGAGTGTGG 1560 CCAGGAGTTT GGGAGTAGGG TGGGTCTAGG CAGGACAGTA CAAGGACACT GACCCTCAGC 1620 CACCCCAGGC AGAGGGGCAG CCTTGGCCCC CGGGCACTGT GACTTGCCCA AGACCACACT 1680 GTGAGTCACC AGGAAAGGAG GAACCAGTGA CAGCCGTGAC TTCACAAGTT GCCCAACAAG 1740 AGCTTGGGCC GGACAAGTTA CCCTAATGAT TAGCACAGGT CTCAAGTTCT CTTTGGTGGG 1800 CAGAAGGCCG TGGTTTGACT GAGCTGGAAG CTGAGAGGAC ACGGCCCCTG CCTCCCCACT 1860 GGAGGCACAA AGGGGAGATC CCCACTTCTC ATCCCCTCGA GTGGCCCAGG CTCCCTCCAG 1920 GCCCCAGGGG AAGAATCGGG GCTGTGTCTG CGGCCGACCT CACATCCCGG TCAAACAATC 1980 CCAGCCCACG TTCCTCCCAA GATCCCTGCC TTCCAAAGCA CTTTCACATC TGCTGTTGGC 2040 TTTGCACACA AATAACCTTC CGGCTGCTGC TGTGCCCCAT CTCACAGAGG CAGAAACGGA 2100 GCCAGCCTCG GAGTGAACGT CAGTTACATT TGCCTGGAAA GTGGATTCCA GCTCCCTTAC 2160 TCCTCACTCT TGCGGCATCT CCCCAGGGTA CCCCCAGCCA TTTGACAGAG AAGGAAACTG 2220 AGGCCCAGAG CAGGACAGGG ATTTGCCCAG GGTCCCCCAG AGAGGTGGAG AGCAGGAGTT 2280 CTTTCATTTG TGGGGCTCCG TAGATGACGG GTCACCGCAG ACATTCACAC TCACACAAGC 2340 ACGCACGCAC ACACACCCGG GGCCCGCACA 2370
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