Tag | Content |
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EnhancerAtlas ID | HS129-03090 |
Organism | Homo sapiens |
Tissue/cell | MCF10A |
Coordinate | chr1:205262580-205265280 |
Target genes | Number: 15 | Name | Ensembl ID |
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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) |
FOSL2 | MA0478.1 | chr1:205263880-205263891 | GGATGACTCAT | + | 6.62 | IRF2 | MA0051.1 | chr1:205263976-205263994 | GGAAAGAGAAAGGAAAAG | + | 6.03 | JUN(var.2) | MA0489.1 | chr1:205263882-205263896 | ATGACTCATCCCCC | - | 6.22 | JUNB | MA0490.1 | chr1:205263880-205263891 | GGATGACTCAT | + | 6.62 | PRDM1 | MA0508.2 | chr1:205262631-205262641 | GTGAAAGTGA | - | 6.02 |
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| Number of super-enhancer constituents: 23 | ID | Coordinate | Tissue/cell |
SE_02431 | chr1:205262567-205264599 | Astrocytes | SE_05801 | chr1:205262462-205264469 | Brain_Hippocampus_Middle | SE_11085 | chr1:205262547-205264187 | CD20 | SE_26974 | chr1:205262635-205264492 | Esophagus | SE_29391 | chr1:205262567-205264765 | Fetal_Intestine_Large | SE_32765 | chr1:205262511-205264574 | H1 | SE_38936 | chr1:205262243-205265794 | IMR90 | SE_46173 | chr1:205262329-205265260 | Osteoblasts | SE_50327 | chr1:205262518-205264578 | Sigmoid_Colon | SE_52983 | chr1:205262582-205264598 | Small_Intestine | SE_54130 | chr1:205262477-205264677 | Spleen | SE_55645 | chr1:205263252-205263684 | Thymus | SE_56704 | chr1:205262588-205264656 | u87 | SE_56704 | chr1:205264714-205265918 | u87 | SE_58462 | chr1:205242169-205295027 | Ly1 | SE_58967 | chr1:205242236-205295022 | Ly3 | SE_60263 | chr1:205242326-205284722 | Ly4 | SE_60576 | chr1:205242267-205294889 | DHL6 | SE_61365 | chr1:205242037-205294994 | HBL1 | SE_61423 | chr1:205183427-205322469 | Toledo | SE_62465 | chr1:205242393-205294944 | Tonsil | SE_65493 | chr1:205262566-205265065 | Pancreatic_islets | SE_68815 | chr1:205262515-205265189 | H9 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr1 | 205262860 | 205263030 | chr1 | 205262798 | 205264485 |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I205293 | chr1 | 205262232 | 205274585 |
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Enhancer Sequence | ATGTGTTGTC TCATTTAATC CTTGCAGTAA TGTGATGGGT GTGAGCTGAC TGTGAAAGTG 60 ACTCTCTAAG TCATTGCAAT GCACTCTGTG GGAAGAATGT GCTAGCCCAG CAAGGCTGTC 120 TTTGTGATGT CCGATGTGTA CGTGCGTGGG GAGGCGCTCC CAAAAGCTGC GCTGGGGCAG 180 GGTGTCCTGA ACGGCGTTAC CAGATGTATC TTGACAAAGA GGTTGGCACC ACCATGAAGA 240 CCAATTCAAC CAGCTCTCCT AGCCCAGCTT CCATGCTCTT CAAGGAGACT TCCCACTGAA 300 CTTCCGAATA CCCTTGTGTG AAACTGCCAC AGGCAGTGAA TGTGCTCATC AGCAAACCCA 360 AGTATCTGGT TGGTTTGACA GGGGTTTTGT TATTCATTAG AAATGAATGA ATTGGCATGT 420 TGGCTGAATC CATTCCTCTC CTAGAGCTCA GTGAGTCTGC TCCTGAGCCT CCTAGCCTGT 480 TGATAAGCAA GGTTTCTGAG CAGCAAAGTG AGGCTGCTCA CTTTGGCAAA CAGGTCTTCA 540 GGTGAGCCCG GCCACCATGT GAGGCCCTGT TGGCAGGCCA GGCTCTCCCC AGGCCCCACC 600 TGGCCTCACC AATGGCTCTT GGATTCACAG AGGACTGCAC ATTGGACTGG GAGACAGGGC 660 AAGCCAGGGG TCCCTTAGCA GAGAAGGGAT CCCTGCCAGT AACTAGCCTG CTGTGAGTAT 720 GAAGTTGCCA CTTACCAAGG ACCCTCCTGA TGGACACAAC AAAGGCGATG GGTGATTGCT 780 GCCAGGGCTC ATAAAGAGGT GATTCAGAAT CTAGCTGGGG GAACTTTGAA AGGTCATTGC 840 ACCTTGACCC TAGCTTCCAG GCGGGACATG TGGTGAGTTC TGCTGCAATG GCTGGGTGCC 900 CTCACAGGCC AGAGCTCAGG TTAATGCAGC TCAGAGCTCG AATTCTGATC ACAGGAAGAG 960 AATGGTGAGG AGGATGGAGG CAGGGGTGCT GGCTGGGCCC AGAACACCAA AGGCAGAGCT 1020 GAACACTTCC ACTGGGAAGT GGGGGTTTTG GCCTCTTGGG CTGGGAAATT CCTGGCCGGC 1080 ACTGTCTGTT TATCAGGGAA GCTGAGTCAG ACTGAAACGT ATCTCCTAAA AAGCTCTGCT 1140 ATTTCTAGGA TTCCATCCGG TCAAAGCCAG CCTCCTCTTC CCTGGGGAAT TCCTTTGAGG 1200 GTGGAGAGAT AGAGGGGACA GACTGGCCTT TTCCTAGACA TGGAAACCTG AAATCTGAGT 1260 TTTTGCCCAT TTATGGACCT GAAATCCCCT CCCCCACCTA GGATGACTCA TCCCCCAGCT 1320 TGACCCAACT GCCCCTAGAG AGGGGAAAGG GTGAAACTGA GATGGTGGGA TTAGCTCAGG 1380 GAGGGGGTTG GAGGCTGGAA AGAGAAAGGA AAAGACAACT GAAAAGGATG GGGAATTCCT 1440 TTGCAAAGAG ATGGTGAGGA GAGGATTTCA GAGCCAAAAA GAGGCAGAAT GAGAAAGAGA 1500 GAAAGATTTT CATCCCAGAG GGAAGCTGCA TGCCTGGCAG AGTAAAAATC TTCCAGGTTA 1560 AGGTAGGTTC AGGCCCTCAC CTTGAGTAAA TTCTGGAACT TTAGTGTGAT CAGAGCCACT 1620 TGCCGTGCTT GTGAAAATGC AGAGATTCCC GTGCCCTCCC TGGGCTGTGA TCCGCTTCCA 1680 GGCTCCTTCA GGGATCTGAA GTAGGAAGTT CTGAAACACA GAAAGAGGAT TGACTGGGAA 1740 TCCTTCTCCC AACCTGGGGC CTCTGCTGTA TAAAGCGACT CACAACCCCT CTGCAGGTGC 1800 CAATGTCAGA GGCAGAGCCC TGGTCCAAGG GTGACGTTTC TAACATTCTT ATAAAAATCT 1860 GTGAAAGACT TTGGCCAGGC CCAGTGGCTC AAGCCTGTGA TCCCAGCACT TTAGGAGGCT 1920 GAGGCAGGTG GATCTCTTGA GGTGAGGAGT TCGAGACCAG CCTGGCCAAC ATGGCAAAAC 1980 CCGTCTCTAC TAAAAATACA AAAAAATTAG CTGGGTGTGG TGGCATGCAC CTGTAGTCCC 2040 AGCTACTGGA GGAGCAGGGG GGCGCTGAGG TGGAGGATCG CTTGTGCTCA GGAGGTCGAG 2100 GCTGCAGTAA GCTGAGATTG CACCATTGTA CTCCAGCCTG GGCCACAGAG TGAGATCCTG 2160 TGTCAAAAAA AAAAAAGACT TTTTATCGGA TGGAGAAAGC CAGTCCCCAC CAGGCCAAAT 2220 ATGCCTCCTC ATTGCAGCAC TGCCCACCTC CCCACATAAT CATATCAGAG AAGCTTTGGA 2280 AAGAACTGCT TTCCTAGTCA ATACAATCCT AGGATCTTTA CAGCCAGAAG GGACTTCTTC 2340 AGGTATCATC TGGCGGGATT TTTCACCTGA AGCAGAAATT CCTTCTAGCA ACAACCCCCA 2400 CATCTCTATC TCCAACCCAA ATCTCTCAAA CTCCAGGCTC CTCATACCAC TTATCTTTGC 2460 CTGGAGGCCT AAGTGCCTCT GACTTCACCT CACACCTCCT CCATCTGCAA GTCTTCCCCG 2520 ACCCAGCTAA TGGACACTCT ACCCTCCAAG TTTCTCAGGC CAGAGACCAT GGAGTGATTC 2580 TTGGTTTCTC TCTTTCTTTC ATACCCTACA TCTAATCCAT CAGGAAAGCC TGTTGGCTCT 2640 AGCTTCAGAA TATGTCAGAA ATCTGACAAC TTGTCATTTC TTTACTACTG ACTCCAGTCC 2700
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