Tag | Content |
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EnhancerAtlas ID | HS030-02127 |
Organism | Homo sapiens |
Tissue/cell | CyT49 |
Coordinate | chr1:205262530-205265780 |
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: 24 | 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_26974 | chr1:205265274-205265884 | 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: 3 | Chromosome | Start | End |
chr1 | 205262860 | 205263030 | chr1 | 205265393 | 205265497 | chr1 | 205262798 | 205264485 |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I205293 | chr1 | 205262232 | 205274585 |
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Enhancer Sequence | TCTCACTCCT TAGGTTTTCT CCAGTGATGT ATTGCTTAAA AAGCATGTTC ATGTGTTGTC 60 TCATTTAATC CTTGCAGTAA TGTGATGGGT GTGAGCTGAC TGTGAAAGTG ACTCTCTAAG 120 TCATTGCAAT GCACTCTGTG GGAAGAATGT GCTAGCCCAG CAAGGCTGTC TTTGTGATGT 180 CCGATGTGTA CGTGCGTGGG GAGGCGCTCC CAAAAGCTGC GCTGGGGCAG GGTGTCCTGA 240 ACGGCGTTAC CAGATGTATC TTGACAAAGA GGTTGGCACC ACCATGAAGA CCAATTCAAC 300 CAGCTCTCCT AGCCCAGCTT CCATGCTCTT CAAGGAGACT TCCCACTGAA CTTCCGAATA 360 CCCTTGTGTG AAACTGCCAC AGGCAGTGAA TGTGCTCATC AGCAAACCCA AGTATCTGGT 420 TGGTTTGACA GGGGTTTTGT TATTCATTAG AAATGAATGA ATTGGCATGT TGGCTGAATC 480 CATTCCTCTC CTAGAGCTCA GTGAGTCTGC TCCTGAGCCT CCTAGCCTGT TGATAAGCAA 540 GGTTTCTGAG CAGCAAAGTG AGGCTGCTCA CTTTGGCAAA CAGGTCTTCA GGTGAGCCCG 600 GCCACCATGT GAGGCCCTGT TGGCAGGCCA GGCTCTCCCC AGGCCCCACC TGGCCTCACC 660 AATGGCTCTT GGATTCACAG AGGACTGCAC ATTGGACTGG GAGACAGGGC AAGCCAGGGG 720 TCCCTTAGCA GAGAAGGGAT CCCTGCCAGT AACTAGCCTG CTGTGAGTAT GAAGTTGCCA 780 CTTACCAAGG ACCCTCCTGA TGGACACAAC AAAGGCGATG GGTGATTGCT GCCAGGGCTC 840 ATAAAGAGGT GATTCAGAAT CTAGCTGGGG GAACTTTGAA AGGTCATTGC ACCTTGACCC 900 TAGCTTCCAG GCGGGACATG TGGTGAGTTC TGCTGCAATG GCTGGGTGCC CTCACAGGCC 960 AGAGCTCAGG TTAATGCAGC TCAGAGCTCG AATTCTGATC ACAGGAAGAG AATGGTGAGG 1020 AGGATGGAGG CAGGGGTGCT GGCTGGGCCC AGAACACCAA AGGCAGAGCT GAACACTTCC 1080 ACTGGGAAGT GGGGGTTTTG GCCTCTTGGG CTGGGAAATT CCTGGCCGGC ACTGTCTGTT 1140 TATCAGGGAA GCTGAGTCAG ACTGAAACGT ATCTCCTAAA AAGCTCTGCT ATTTCTAGGA 1200 TTCCATCCGG TCAAAGCCAG CCTCCTCTTC CCTGGGGAAT TCCTTTGAGG GTGGAGAGAT 1260 AGAGGGGACA GACTGGCCTT TTCCTAGACA TGGAAACCTG AAATCTGAGT TTTTGCCCAT 1320 TTATGGACCT GAAATCCCCT CCCCCACCTA GGATGACTCA TCCCCCAGCT TGACCCAACT 1380 GCCCCTAGAG AGGGGAAAGG GTGAAACTGA GATGGTGGGA TTAGCTCAGG GAGGGGGTTG 1440 GAGGCTGGAA AGAGAAAGGA AAAGACAACT GAAAAGGATG GGGAATTCCT TTGCAAAGAG 1500 ATGGTGAGGA GAGGATTTCA GAGCCAAAAA GAGGCAGAAT GAGAAAGAGA GAAAGATTTT 1560 CATCCCAGAG GGAAGCTGCA TGCCTGGCAG AGTAAAAATC TTCCAGGTTA AGGTAGGTTC 1620 AGGCCCTCAC CTTGAGTAAA TTCTGGAACT TTAGTGTGAT CAGAGCCACT TGCCGTGCTT 1680 GTGAAAATGC AGAGATTCCC GTGCCCTCCC TGGGCTGTGA TCCGCTTCCA GGCTCCTTCA 1740 GGGATCTGAA GTAGGAAGTT CTGAAACACA GAAAGAGGAT TGACTGGGAA TCCTTCTCCC 1800 AACCTGGGGC CTCTGCTGTA TAAAGCGACT CACAACCCCT CTGCAGGTGC CAATGTCAGA 1860 GGCAGAGCCC TGGTCCAAGG GTGACGTTTC TAACATTCTT ATAAAAATCT GTGAAAGACT 1920 TTGGCCAGGC CCAGTGGCTC AAGCCTGTGA TCCCAGCACT TTAGGAGGCT GAGGCAGGTG 1980 GATCTCTTGA GGTGAGGAGT TCGAGACCAG CCTGGCCAAC ATGGCAAAAC CCGTCTCTAC 2040 TAAAAATACA AAAAAATTAG CTGGGTGTGG TGGCATGCAC CTGTAGTCCC AGCTACTGGA 2100 GGAGCAGGGG GGCGCTGAGG TGGAGGATCG CTTGTGCTCA GGAGGTCGAG GCTGCAGTAA 2160 GCTGAGATTG CACCATTGTA CTCCAGCCTG GGCCACAGAG TGAGATCCTG TGTCAAAAAA 2220 AAAAAAGACT TTTTATCGGA TGGAGAAAGC CAGTCCCCAC CAGGCCAAAT ATGCCTCCTC 2280 ATTGCAGCAC TGCCCACCTC CCCACATAAT CATATCAGAG AAGCTTTGGA AAGAACTGCT 2340 TTCCTAGTCA ATACAATCCT AGGATCTTTA CAGCCAGAAG GGACTTCTTC AGGTATCATC 2400 TGGCGGGATT TTTCACCTGA AGCAGAAATT CCTTCTAGCA ACAACCCCCA CATCTCTATC 2460 TCCAACCCAA ATCTCTCAAA CTCCAGGCTC CTCATACCAC TTATCTTTGC CTGGAGGCCT 2520 AAGTGCCTCT GACTTCACCT CACACCTCCT CCATCTGCAA GTCTTCCCCG ACCCAGCTAA 2580 TGGACACTCT ACCCTCCAAG TTTCTCAGGC CAGAGACCAT GGAGTGATTC TTGGTTTCTC 2640 TCTTTCTTTC ATACCCTACA TCTAATCCAT CAGGAAAGCC TGTTGGCTCT AGCTTCAGAA 2700 TATGTCAGAA ATCTGACAAC TTGTCATTTC TTTACTACTG ACTCCAGTCC AAGCCCCATT 2760 ACCTCTTTCC AGAATTGGAC AATGTCGACC CTCCCATGGC TAGTCTCAAC AAGCAGAAGA 2820 ATTTTTTTTA ATTCTATCTC AAAAAAAAAA AATGTCATTC CTTTGCTCAG AACTTCCTGG 2880 TGGTTGGCAA TTTCATTCTG AATAAAAGCC ACAGCCCATG TAATGGTTCA CAAGGCCCTG 2940 TGTAATCTAC CTTCCCCACC CTTGTTACCT CTCCTGACAC GTCTTCTGCT ACTCTCTCAT 3000 GCACTCTGCT CCAGCATCAA TGGCTGTTCT AGAACTTGCA ACCTGCTCTT GCCTTGAGGC 3060 CTTTGCAATG GTTGTTCCCT CCACCCTGAA CACTGTTCCC CCAGATAGCC ACATAGCTAG 3120 CTCCACCCCC AACCCCTGCC ACCAGGTTTT TATTCAAATG CCACCTTCTC AGGAAGGCCT 3180 TCTCTGATCA CCCTTATTTA AAATTTCAAT CCTGTCTCCT CTCCATCCCC ATACCCCATC 3240 CTTATTATTA 3250
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