Tag | Content |
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EnhancerAtlas ID | HS165-12972 |
Organism | Homo sapiens |
Tissue/cell | Ramos |
Coordinate | chr6:30483590-30484910 |
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) |
FOXP1 | MA0481.2 | chr6:30484034-30484046 | AGGTAAACAGAA | + | 6.14 | POU4F2 | MA0683.1 | chr6:30484255-30484271 | GAGAATATTTAATGAA | + | 6.09 | TEAD1 | MA0090.2 | chr6:30484184-30484194 | CACATTCCAT | + | 6.02 |
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| Number of super-enhancer constituents: 6 | ID | Coordinate | Tissue/cell |
SE_20955 | chr6:30483089-30484988 | CD8_Memory_7pool | SE_51043 | chr6:30482661-30484841 | Sigmoid_Colon | SE_53014 | chr6:30482775-30484845 | Small_Intestine | SE_53611 | chr6:30482485-30485328 | Spleen | SE_62602 | chr6:30456364-30512797 | Tonsil | SE_65627 | chr6:30483105-30485215 | Pancreatic_islets |
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Enhancer Sequence | TCACCGCAAC TTCCGCCTCC CAGGTTCAAG CGATTCTCCT GCCTCAGCCT CCCGAGTAGC 60 TTGTATTACA GGCATGCGCC ACCACACCCG GCTAATTTTG TATTTTTAGT AGAGAGGGGG 120 TTTCTCCATG TTGTTCAGGC TGGTCTCGAA CTCCCAACCT CAGGTGATCC GCCTGTCTTG 180 GCCTCTCAAG TGCTGGGATT ACAGGGGTGA GCCACCGCGC CCAGCCGGGA GCCCCTATTT 240 TAAGGACGCT ATTGCTGTGG AGGAGTAACC CCACTTTTAG GAATCCTTTT CCGTGCGAAA 300 GGCTGTTTGA GATCAGGCGC AACAACTTCT CCCGCTCAGG TTACCCTCAG AAAGGCTATG 360 GACCCCGGAC TCCGCCCCAG ATTGCATAAC AACTGAGGGG TGGGTCCCTA TTTCCTCTCT 420 GGGATCTGTA GCCAATCATT CACGAGGTAA ACAGAACGAC CGAGTTTCTC TCAGCCGAGA 480 ACTGTGGCTG CCCCTCCGGT GAAAACAGAG GAAGTGGGAG CGGCAGGAAG CGCTTTGGGA 540 CCAGGGCGAC CCCTGAAGCG TAGAGGAACC AGGTCACAAG CATACGTGAA TGCTCACATT 600 CCATAGTTAT CAAATGTATT CAGGTTTAAA TTTTACTTTT CTAGAAAAAA TGTAAATAAT 660 CCGTTGAGAA TATTTAATGA AAAATGTTGG TCGTATCTTT ATCTGGTCTG CGGCTCTGTC 720 CCTGTTTCCT GGATAGGAGA CTACGTCTGT ATCTTGTATC ACAGGAGGCA CCTTCTTCCT 780 GTTTCCTGGC ACAGACTTGT AAGTGAATTT CCTGCCCGCC TCCGCCCACA GCGTAAGCCG 840 CGCTGGAACA GCTCACTTAT TGCCCCAGAT GTATGTGGAG TAACCGCCTT CAGTTTCCTG 900 GTTCTGAGTT TCCGTGTTAC TCAAGCAATG CTTCTGCTGA ATTTGTCTTT TTTTTTTTTT 960 TGAGACAGAG TCTTGCTTTG TCGCCCAGAC TGGAGTGAAA TGGCGTGGTC TCGGCTCACT 1020 GCAGCCTCCA CCTCCTGGGT TCAAGCGAGT CTCCTGCCTC AGCCTCCTGA GTGTGCAACT 1080 TATCTTTTTA TTTTATTTAT TTATAATTTT TTGGCTAATT TTGGCTATTT TGTGTCTGTG 1140 TGTGTATTTT TAGTAGACAT GGGGTTTCAC CATGTTGGGC AGGCTGGTCT CGAACTCCTG 1200 ACCTCAGGTG ATCCGCCCAC CTCGGCCTCC CAAAGTGCTG GAATTACAGG CGTGAGCCAC 1260 CGCACCTGGC CTATTTATTT ATTTATTTAT TTGTGACTGA GTCTCGCTCT GTCACCCAAG 1320
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