Tag | Content |
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EnhancerAtlas ID | HS092-09525 |
Organism | Homo sapiens |
Tissue/cell | HFF |
Coordinate | chr11:66368590-66370850 |
Target genes | Number: 46 | 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) |
Nr2f6(var.2) | MA0728.1 | chr11:66368781-66368796 | TGAACTCCTGACCTC | - | 6.22 | ZNF263 | MA0528.1 | chr11:66369022-66369043 | CTTTCTCCCCTCCCCTCCCCT | - | 6.27 | ZNF263 | MA0528.1 | chr11:66369017-66369038 | TTTTCCTTTCTCCCCTCCCCT | - | 6.3 | ZNF263 | MA0528.1 | chr11:66369027-66369048 | TCCCCTCCCCTCCCCTCCCCT | - | 6.91 | ZNF263 | MA0528.1 | chr11:66369034-66369055 | CCCTCCCCTCCCCTCTCCTTT | - | 6.91 |
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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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| Number: 2 | ID | Chromosome | Start | End |
GH11I066600 | chr11 | 66367595 | 66368803 | GH11I066601 | chr11 | 66369061 | 66370282 |
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Enhancer Sequence | TTTGTTCTTA TTGCCCAGGC TAGAGTGCAA TGGCGCAGTC CCAGCTCATT GCAACCTCCG 60 CCTCCCAAGT TCAAACGATT CTCCTGCCTC AGCCTCCCTA ATAGCTGGGA CTACAGGTGC 120 ACACCACCAC ACCCGGGTAA TTTTTGTATT TTTAGTAGAG ATGGGGTTTC ACCAGGTTGG 180 CCAGGCAGTC TTGAACTCCT GACCTCAAGT GATCCACCCA CCTCAGCCTC CCAAAGTGCT 240 GGGATTACAG GCGTGAGCCA CTGTGCCCGG CTCTGACTGG GCTATTTTCT ATCTTGATGG 300 GTTTGCAACC TTGTGCCACA AAACAATTGA AACCATGGTA TGTGTTGCTT AATGCATGTT 360 ACTGATTTTT TGGACTTTTC ACAGCTCTGT TACCTATCAT GCTTTTCTTT TCTTCTGTTT 420 CTTTTCCTTT TCCTTTCTCC CCTCCCCTCC CCTCCCCTCT CCTTTCCGAG ATAGGATCTC 480 ACTCTGTTGC CCATGCTGGA GTGCAGTGCT GTGATCATGG CTCACTACAG CCTTGAACTC 540 ATGGGCTCAA GCAATCCTCC CACCTCACCT GATAGCTGGG ACCACAAGCA TGTACCATTA 600 TGCCCAGCTA ATTTTTTTTT TTTGTTTTTT TGGTGGTAGA AATAGGGTGT CACTATGTTC 660 CTCAGGCTGG TCTCAAACTG CTGGGCTTGA GCAGACCTCC CTCCTCGGCC TCCCAGTGTT 720 AGGATTATGA GCATGAGCCA GCATGCCTGG CCTCTGCCAC ATTTTTTTTT TTTCTTTTTC 780 TTTTTTTTAT TTTTAGTAGA AACGAGGTTT TGCCATGTTG GCCAGGCTGG TCTTGAAGTC 840 CCAACCTCAA GTGATCCGCC TGCCTTGGCC TCCCAAAGTG CTGGGATTAC AGGCATGAGC 900 CACTGTGCCC AACCACCCTG TCACATTTCT AATGATCAAA AGTTTTTACT CCCTGTTCTG 960 GGAAATTGGA GAGGCATTTC TTATAGAGTC CATTGCACAG TGCCATGCTT ATGCTCAGTG 1020 ATTAGTAATC TGCTGCTGCA AATCAAATGA CTCCAAAGTT AGGAGTTTAA AACAACAAAC 1080 ATATACTGTC TCTGGGGCAG GAATTTGTGT GTGACTTAGC TGGGTGCCTG CAGCTCAGGG 1140 TCTCTCTCGG GGCTGCAGTC ATCTCAGGGC CCCACGTGGG GAGAATCTGC TTCCAGGTTT 1200 GCTCATGTTG CTGTTGGCAG GCCCCAGGTC CTCCTTGGCT GTTGGCCAGA GACATCAGTT 1260 CTTTGCCACA TGGGTCTCTC CCTAGGGCAG CTAACAACAC GGCAGTTGGC TTCTCTCAGA 1320 GTGAATGAGC GAGAGAGAGA GAGATTGAGA TTGAGAGAGG GCGTCCAAGA CTCAAGCCAC 1380 ATTCTTTTTG TAACCTAATC TTAGAAGTGA CACTAGGTCC AGCCCACACT CAAGGGAGGC 1440 ACATCATAGA GGCCATTCGC CTCATGCAGC CTTGAAAGAT GATGGGCAGG AAGTAGGCAT 1500 TGAAGAGGGT AAGAGTGGGA TTGGCAAGCC CAGCAAAAGA AACTGCCCGG GCAAAGCCCT 1560 CAAGGCATGG AATGGCAGGG AGTGTTTCTG AAGGGCAGGA GCCTGTCTTG TGACCTGTGT 1620 TTTCTTCCTG GGCCCCAGGT GGGGCAGGGA ATCAGAAGGG GCTGGCATCA GCAGCTGTAC 1680 CTCACCCAAT CCCTTAACTT AGACAAGGAA GAACTGAGCA GGAGCTGACC AGCCAAGGCC 1740 ACGGTGACTG GCAAGTTGCT GTTGGGTTTT AGCATCTGCT TTTCCCAGGT GGAAAAGAAT 1800 TCCATGTGGG AATTTGCATT CAAGCCTGGT TGTCCCTTGC ACATCTCCTA ACTGATCTCT 1860 AAGCTCCCTT CTGTTCTCTC CTCACCCTGC TCCAGTCTTT ACTTTTCATA GACTGCACTA 1920 GAAGGATTGT TCTGAAGCCT GGAGTAACCA GGCCATGCCC CTGCCTGAAA CTTGTCTTGG 1980 CTCCCAGTGC CTGAGAGTAC AAGCTGGGCC TAGCTTCTTG ATGTGGACAT TCAATACCCC 2040 ACTCCCCCTG CCTATTGCCC CTGCCTGTGT GCTGAGGAAA CAGCCTGGAA AGGCTGCCTT 2100 TCCCTGAACT CCTGCTGGGT CATGCCTCCA GCCACACTGT CCAGGCTGCC CCCTGCCTTG 2160 AGGCCGCTCC TCCAGCCGGG CACAGTGGCT CACGCCTGCA ACCCTAGCAC TTTGGGAGGC 2220 CGAGGCAGAC GGATCACTTG AGTTCAGGAG TTCGAGACCA 2260
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