Tag | Content |
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EnhancerAtlas ID | HS129-06202 |
Organism | Homo sapiens |
Tissue/cell | MCF10A |
Coordinate | chr11:18288530-18290740 |
Target genes | Number: 16 | 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) |
IRF1 | MA0050.2 | chr11:18289604-18289625 | TGGGACTTTCAGTTTCTCTCT | + | 6.65 | IRF1 | MA0050.2 | chr11:18289921-18289942 | AAAATGAAAAAGAAAGTGCAG | - | 7.26 | ZNF263 | MA0528.1 | chr11:18289103-18289124 | CTTCTTTCTCCTTCCTCCTTC | - | 6.98 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr11 | 18289837 | 18290122 | chr11 | 18289126 | 18290255 |
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| Number: 1 | ID | Chromosome | Start | End |
GH11I018267 | chr11 | 18289241 | 18290590 |
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Enhancer Sequence | GCTTCAGAAG GTTTGCAGGA TTTCTGAAGA GAAACATCAC CCTGGACCTG ATAAACTGGG 60 GAAAATGATG CTTTCGGAAG GCTGCTTTTG AACCACAGAG TTGCTAGTGT CTGCGTTGCT 120 GAGGCCTGCC AGGAACTAGG GTTTGCTGGG TTGCCTGTCT CGAGTCTTTC AGAGCTGCTG 180 GGAATATCCC CTTTCCCCGT AGTGCAGCTT CTCAGGATGT GTTAAGTGGA TGGATCACAT 240 TTCAGAAGCC GCTGCAAGGT GTATCAAAAA CACATCTCCT GAGCCGTAAG GGACGGGGCA 300 TCCAGTAACA ACGCACACGG GGTATTTTTG GGCTTCCTTA AGATTTGAGC CGCTGCCTTA 360 GGTTGTGCTG CCCAATGTGC CTGGGGAGCT GCTAAACAGA TTAGAGAGTC GAGGATTGTT 420 GTCAGTTACT CAGAGAAAGA ACAATCATCC TTTCCAGGAG CACCTGAGCT GTTTGTTTTG 480 CGTAGAAGAT GCAAAATAAG GCCTGCAATG GGTATAAAAT GTCCCTCAGC ATAAATCGCA 540 TAGGAGTATG ACTAAGGCTG TTGACTCTTC TGTCTTCTTT CTCCTTCCTC CTTCGATTTC 600 CTAGTTGGAT AATGTACAGG GCTCTTTAGC CTCGCTCTGT CAGGGGCTCC CTTCCTGGTT 660 TGTTCTGTTT CCATTCTTCC TTCTCCAGCC TTCTTGACAA GAGCTGGGAA CTAACGTGCC 720 TCAAGCCCCC ACAAGGACCA CAGCATTTTC TCATTTAGTT TCAGAATGAC TCTGTGACGC 780 AATCTTCCTC TCTTGGAAGG TGAGAAAGCT GATCTTGGAA GGTGAGAAAG CTGAGACTTA 840 GAGCAGCTGA AGCCAATGCC CAGGGACTTA CTGCCAGTCA GCAGGTGGCA GGGCAGAGGT 900 TTGAGCCCGG CTGTGCTTGA GGTCAGGGCT CTTGCCAGGT AGACGCATCA CTGACCACCT 960 CCTAGAGGTT GATGGTTATG AATCTCAGGC ACACCTTGGC ATCACCTGAA ATACCCATGC 1020 CTTCAACTCC CCAGCAGAGT CTGCAGAAAC TGGCCTGGGG TGTGGCCTGG GCACTGGGAC 1080 TTTCAGTTTC TCTCTGGGTG ATTAGAAAGT GCAGCCAAGG CTCACGCCTG TAATTCCAGC 1140 ACTTTGGGAG GCCAAGGTGG ATGAATCACT TGAGGTCATG AGTTCCGGAG CAGCCTGGCC 1200 AACATGGTGA AACCCCGTCT CTACTAAAAA TACTAAAATG TAGCCAGGCG TGGTGGCAGG 1260 CACCTGTAAT CCCAGCTACT CAGGAGGCTG AAGCACGAGA ATCACTTGAA CCCGAGAAGC 1320 AGAGGTTGCA GTGACTAGAG ATCGCACCAG TGTCCTCCAA CCTGGGTGAC AGAGCGAGAC 1380 TCCATCTAAA AAAAATGAAA AAGAAAGTGC AGCCAAGGCA GAGCACCACT GCCCTATTGC 1440 TTCCTCAAGC AACCCACAGC ATCAGTACAG CCTACTAAGA AAGTATTTAG GGACTTTTAT 1500 GCTCCTAACA GTCACTGGAA CTCACGTCAC AATGACGTGT ATTCCATTTG CAAGAATATA 1560 TACTTTAGGT CGGGGTGCGG TGGCTCACGC CTGTAATCCC AGCACTTTGG GAGGCCAAGG 1620 CAGGGGGATC ACGAGGTCAG GAGTTCGAGA CCAGCCTGAC CAACATGGTG AAATCCCCGT 1680 CTCTACTAAA AATACAAAAA TTAGCCAGGC GTGATGGCGC ATGCCTGTAA TCTCAGCTAC 1740 TCAGGAGGCT GAGGCAGAAG AATCTCTTGA ACCTGGGAGG TGGAGGTTGC GATGAGCTGA 1800 GATAGCACCA CTGCACTCCA GCCTGGGCGA CAGAGCAAGA CTCTGTCTAA AAAAAAAAAA 1860 AAAAAAAAAA AAAAAAAAAA GAATATAAAC TTTAGTAGTC AGGGCAGAAG TACTCTGTGT 1920 CTGCCACCTT TCTCAGCATC AGTATTCCAT GTCACTACCT CATTCATACA CACTCCTGGA 1980 TCTTATCATA GGCAGCTTCA TTCTATAGCA GTGGCTCTTC ACCAGGGCAC TTGAAGAAGC 2040 CAACTAGGAT AAAGGAATGT GCTTCTCAAC CCATGGTATC CAAGGCTGCT ATGATCACAG 2100 GCTGAAAGCT TGAAGTCAGT GGAAGATTTG TCCTTCCTCA TTCCCCTCTA AGGTGTTGTT 2160 GGAGTCTTTA TGTTCTCCTG ATGTCCCTTC TGCCTTTCCT TTCCTTTCCA 2210
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