Tag | Content |
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EnhancerAtlas ID | HS026-00222 |
Organism | Homo sapiens |
Tissue/cell | CNCC |
Coordinate | chr1:10563460-10565460 |
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) |
EWSR1-FLI1 | MA0149.1 | chr1:10564253-10564271 | CCTTCCTTCTTCCCTCCC | - | 6.84 | EWSR1-FLI1 | MA0149.1 | chr1:10564827-10564845 | TCTTCTTTCCTTCCCTCC | - | 6.96 | IRF1 | MA0050.2 | chr1:10564805-10564826 | TCTTTCTTTCCTTTTCCTTTT | + | 6.06 | ZNF263 | MA0528.1 | chr1:10564832-10564853 | TTTCCTTCCCTCCCCTCCCCT | - | 6.44 | ZNF263 | MA0528.1 | chr1:10564837-10564858 | TTCCCTCCCCTCCCCTCCCCT | - | 6.45 | ZNF263 | MA0528.1 | chr1:10564827-10564848 | TCTTCTTTCCTTCCCTCCCCT | - | 6.49 | ZNF263 | MA0528.1 | chr1:10564844-10564865 | CCCTCCCCTCCCCTCTCCTCT | - | 7.39 | Zfx | MA0146.2 | chr1:10564034-10564048 | CCCGCCTCGGCCTC | + | 6.01 |
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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 | TGGGGGCTTT TAGATTTATC CTGAGTTTGC TAATCTTAGA GCTCCTTTAC ATGCCCTACC 60 ATTGCTGAAG ACGTGATCTA CAAAACTTTT ATTTGGGCAG AGGAAATAAA ATTTCCTCTG 120 TTAAAATGTT TTTCTTTTGA TTAAAATCAG TCATCAGTTT CAAAGAATTT TCATGTAAAA 180 GTGTTTTTTT AAGTGTGATC TAAAGCATAG GTATTCCATG CGGCAAACTC AGGATAAATC 240 TAAAAGCCCC CAGTGTGAAA ACTGTTGACT GTTGTGTTGG TTAAGATAAC CAAGTGCCCT 300 ACATGTTCCA GGATAACCTT TTTTCTTTTT TCTTTTCTTT TCTTTTTTTT GAGACAGTCT 360 TGCTCTGTTG CCCAGGCTGG AGTACAGTGG CACAATCTCA GCTCACTGCA ACCTCTGCCT 420 TGGGGGTTCA AGTGATTCTC ATGCCTAAGC CTCTTGAGTA GCTGGGATTA CAGGCGCCCA 480 CCACCATGCC TGGCTAATTT TTTAATTTTT AGTAGAGATG GGGTTTTGCC ATGTTGGCCA 540 GGCTGGTCTC AAACTCTTGG CCTCAAATGA TCCACCCGCC TCGGCCTCCC AAAGTGCTGG 600 GATTACAGGT GTGAGCCACT GTGCCCGGCC CATTTTCCAG GATAATTGTA ATTTAAAATA 660 TTTTAGCTCA TTGTCAAACC ACGCAGAATG ATTTTTGGCT CAAAAAATAT GATCTTGTAG 720 TTAGTCCCAC TTCTGAGCTG TGAGAAACCG CAGGAAGATA AAGTGGTGCT TTGGAGAAGG 780 ACGTATTCAC CGCCCTTCCT TCTTCCCTCC CAGCTCTCCT TTCTTTTATG GTTTGTAGTT 840 ATAACCGAGA TTTATGCTTG TTGCTCCACA AATCTTCTCT CTGCCATTAT GAGTTTGTCT 900 GAACAGTCTA GAGATGGGGC CGACACTGAG TGATTCTTGA AGTAAATCTA TCCAGGGGCA 960 CTCCTTGACA GTCAGAGGCA GAGAGGAACT AACTCATAGC CCCCAGTGGA GCAGGAGTCT 1020 GGATAAATTA CCCCTGTCAG GAAGAAGACA TGCTGCCACT TTTGTGACCT CTTGCCTTCA 1080 CAGTGACCCT GGGGGCACAG CTCTCCTGTT TGTGTGCAGA GTGTGTGGGG CGGTGCTCTG 1140 GGTCAGCGAT CATTCCCTTT ACCCAGCTGT GTCTGCCAAG AGGCCTTTCT CTCTGTGTTG 1200 GCCCAGCCAG GCCCGTGGCA AGTGGGTCTT TAGGACCAGG GCCACTTTTT GCAGCCGTAT 1260 GGTAGCAAGG AGTTGCTGAC AATCAAGCAC ACAAGTTGAT TGATTCCTTT TCCTTTTCCT 1320 TTCCTTTCCT TTCCTTTCTT TATTTTCTTT CTTTCCTTTT CCTTTTCTCT TCTTTCCTTC 1380 CCTCCCCTCC CCTCCCCTCT CCTCTTTTTG TTTCACTCTG TCAACCAGGC TGGAGTGCAG 1440 TGGTGCCATC TTGGCTCACT GCAACCTCCG CCTCCCAGGG TCAAGCTGTT CTCCTGCCTC 1500 CTCCTCAGTA GCTGAGATTA CAGGTGTGCG CCACCACACC CAGCTAAGTT TTTGTATTTT 1560 TAGTAGAGAC GGAGTTTCAA CATGTTGGCC AGGCTGGTCT CAAAACTCCT GACCTCAAGT 1620 GATTTGCCCA CCTTGGCCTC CCTCCCAAAG TGTTGGAATT ACAGGCATGA GCCACCATAC 1680 CTGGCCAATG ATTATTTCTA TAAATGGTTT CATTTAACTA GCATTTACCG ACAGTGGATT 1740 TTGATGGAGA AGGAGAATAA AGAACAGGTA TTAAACATCT TTTAGGCTAG GTATGGTGGC 1800 TCACACCTGT AATCCCAGCA CCTTGCGAGG CTGAGGCAAG AGAATTGCTT GAGCCCAGGA 1860 GTTTTGAGAT CAGCCTGGGC AACGTGACGA GGTGCCATCT CTATAAAAAA TGCAAAAATT 1920 AGTGGGACAT GTGGCTCGAG CCTGTAGTCC CAGCTACTCT GGAGGCTGAG GCAGGAGGAT 1980 TGCATCAACC CAGGAGATTG 2000
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