Tag | Content |
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EnhancerAtlas ID | HS095-06449 |
Organism | Homo sapiens |
Tissue/cell | HMEC |
Coordinate | chr11:130816280-130818830 |
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) |
NFYA | MA0060.3 | chr11:130817471-130817482 | TCTGATTGGTT | - | 6.62 | NFYB | MA0502.1 | chr11:130817472-130817487 | CTGATTGGTTGAGGC | - | 6.38 | POU2F2 | MA0507.1 | chr11:130817112-130817125 | TTAATTTGCATTT | + | 6.25 | ZNF263 | MA0528.1 | chr11:130818533-130818554 | CCTTCCTTCCCTTTCTGCCTC | - | 6.01 |
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| Number: 2 | ID | Chromosome | Start | End |
GH11I130945 | chr11 | 130815478 | 130816610 | GH11I130947 | chr11 | 130817286 | 130818511 |
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Enhancer Sequence | CATAGGAATT TAACTCTTGT TTATATCAAT TACCAATATA AAGTTGGTTT AATTGTACAG 60 AATTTTGCTT AAAATTGCAA TTTCCAAGAA CCTATCGATG ACACTAAGTG AGGACTTACT 120 GTAGTTGGAA TCACACAGTA CGTAGCCTTT CCAGATTGAA TTATTTCACC TGGTAATATG 180 CATTTAAGGT TTCTTCATGT CTTTTCATGG CTTGATAGCT TATTTCTTCT CAATATTGAA 240 TAATATTCTA TTGTCTAGAT ATACTACAGT TTATTTATCC ATTCACCTAC TGAAGGACAA 300 CTCGGTTGCT TCCAACTTTT CGCAGTTATG AATAAGGCTT AAATAAACAT TTGTGTGCTG 360 GGGTTTTTTC TTGTGGACAT GCTTTCAGCC CCTTTGAGTA AATACAAAGA AGCATGATTG 420 CTGAATTGTG CAGTAAGAAT ATGTCTAGTT TTGTAAGAAA CTGCCAAACT CTTTCAAAGT 480 GGCTGTACCA TTTTGCATAT TTACCAGCAA TGGATGAAAG TTCCTGTTGC TTCACATCCT 540 TGCCTGCATT TGGTGTTTCA AGTGAGCTGT GTGAAAGTGC TCTGTATTTG CACCTCGGGC 600 TCCCTGGAAG GTGAGAGGAG ACCCACTGAT GTAAATTCTC ACATAGGTGG ATGGGAGTCT 660 TAGATGACAG ATAGGCAAGA GGCTGTGGAC GTGGGCACTG GTTTGTTTTT GTACTCCGGC 720 TGAGCCCAGG CAACTCCTTA ATGAGCTCCT CTCAGTAAGA GGGGAGCCTG GGGTGTGGTG 780 TATTTTCTGG ATTTTGGTTA TTCTAACAGG TACATAGTCT CTCCCTGTGG CTTTAATTTG 840 CATTTCCCTG ATGACATGTG ATATGAAGCA TCTGTCCACG TGCTTACTGG CCATCTGCAT 900 ATCTTCTTTG GTAAGGTGTT GGTTCAGGTT TCCATTTTTT AATTGGGTTG TTAGTTTCTC 960 TTAATTGTTG ACTTTTTAAG GGTTATTTTT GTATATTTTT GAATAATAGT CTTTTATTAA 1020 ATTTGTTTTT TGCACATATT TTCTTTCAGT CTATGGCTTC CCTTCTCATT CTCTTGACAT 1080 AGTTTTAAAA AGTCTTGGCT ATAAATCTGA AATCTGATTA TTTGCCTCTT CATGCCAAAA 1140 GGGAAGAAAA GAAAAAAAAT CTAGTTAGTT GAGGATTTAG GTTACTATTG CTCTGATTGG 1200 TTGAGGCTTT CTCATCTCTG GCTTTGGCAG GCAGCGACAT GCCCATTATT TCCCCACCCC 1260 TTAAGTGTGG GTAGAGAAAA AGATGGTCAT GCGCTCACTC TCGCCCCATC TCTGTGCCAG 1320 GTCCCACCCT ATCTGTCCTT ATCCGGCCAA ATCACCGATA TCCAAACACC TGGGTGAGTA 1380 AGAGTGACAA TGAGGCCCTC TGCTCTCTCC CAACATCCCC CAGGCTCTCT GAACAACTGA 1440 TAACCACCAA AAGGTGATTT CTACGTGTAC AACTACATAG AGACAGAGCT TGAATCACCA 1500 GAGACAAGAG GCACCGTATA TTCCTCCTTG GCAGTCTCTT AGGTAATTAT TTGGTGGAAC 1560 GGTGGAAACA ATACTTCTTT GGAGTGGAGA GAGAGAGAGA CAGAGACAGA GAGAGACAGA 1620 CAGAGAGAGA GAAAGAGGGA TTGAGAGAGA GAGAGAGAGA AAGATATTGC GAGAGCCTGT 1680 GAGTCTGTGA GCCAGTGAGT CATGTGAAAG TGCCTAGCAT TTTCACTCGG GGCTCCCTCA 1740 AATGTGAGAG GAGAACCACT GAAGTAAATT CTTCCTGTAG GGGCACAGGA AACTTAGGTG 1800 GCAGACAGGT AAGAGGCTGT GGACCTTGGC TCTGTTTGGG TCTGTACACT GACTGAGCCC 1860 AGGCAAACAG TTACGGGGAA TTTTCCTTAA TGAGCTGCCC GAGCTTGTAA GAGGGGAGCC 1920 CTGAGCCTTG AGGCATGTCT TCTGGGTTAC TTTGGGAAGT GGAAGAAATG AAAAGGCCAC 1980 TTAATTGAGC AAAGAGAAAG GGCCTTGGGA GGACAGTTTC AAAGCATCAG GGAGGGAGGA 2040 CTGAACATAG CTCTTGTGTG ATTCCTGTCC GTTCTTCCTG CCCACTCCAC TGGTTCTGCA 2100 AATAAACCTT GCCTTTTAAG TCTTTATTCT GAAGTCCAAG ACTCTAGCTA TCTTGTTCTA 2160 GTAATCTTTC CACCTAGCTA CATCTCCTTC TATTTCCCTG CATGCATCCT GTCCTGCAGA 2220 GACTTCCATT CTGTCTTCCT GACATGCATG ATGCCTTCCT TCCCTTTCTG CCTCTTTCTT 2280 CTGCATCGGC CTTTAGCCCT CTTGGTCCCG CTTGTTCCTC CCTAATTTTA CCTGAAGGGA 2340 ATTAAAGAAC ACAAGCATAC TAGAAAAAAA GATGATTCTT TTATTCCTTT GTAGTATTTG 2400 GAAAACAGCT TTAAACATGT ATAGGTATAC TAAAGCTGGA AGAGGTCTTG TGAATTTATT 2460 ATTTCCTAAC TTTAGGCAGA AACTCACTGA AACCATTGCC AGGAACACCC AGTTCTCAGA 2520 AAATATTCTT TAGAAATTTC AGTAATATGC 2550
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