Tag | Content |
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EnhancerAtlas ID | HS092-17050 |
Organism | Homo sapiens |
Tissue/cell | HFF |
Coordinate | chr14:103827370-103829600 |
Target genes | Number: 18 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
HSF1 | MA0486.2 | chr14:103828409-103828422 | TTCTGGAATTTTC | + | 6.17 | NFAT5 | MA0606.1 | chr14:103828416-103828426 | ATTTTCCATT | + | 6.02 | NFATC1 | MA0624.1 | chr14:103828416-103828426 | ATTTTCCATT | + | 6.02 | NFATC3 | MA0625.1 | chr14:103828416-103828426 | ATTTTCCATT | + | 6.02 | Nr2f6(var.2) | MA0728.1 | chr14:103829197-103829212 | TGAACTCCTGACCTC | - | 6.22 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr14 | 103828242 | 103828602 | chr14 | 103828081 | 103828691 |
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| Number: 2 | ID | Chromosome | Start | End |
GH14I103360 | chr14 | 103826966 | 103827408 | GH14I103361 | chr14 | 103827555 | 103829319 |
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Enhancer Sequence | CATGGTGAAA CCCCGTCTCT ACTAAAAATA CAAAAATTAG CCGGGCATGG TGGCAGGCAC 60 CTGTAATCCC AGCTACTCGG GAGGCTGAGG CAGGAGAATC ACTTGAACCC AGGAGGCAGA 120 GGTTGCAGTG AGCTGAGATC ACACCATTGC ACGCCAGCCT GGGCAACAGA GCGAGACTCC 180 ATCTCAAAAA AAAAAACAAG TTTTTATTCT GCCCTAACAT TTTGTTGGTA AATTAGCTAG 240 GTATAGAATT TCAAGTTTCA GATTATTTTT ATTGAGAACA TTGAAGGCAT TGCTCCAGGG 300 TCCTCAAGCA TCCAATGAGG CTGATAAATT TGATGTGATT GGATTTTCAT TCCTTAGTAG 360 GTTAATTTCT CTCTCTCTGA GAGCTTTTAG AATTGTCCTG CTTTTTACAT TTTTCTTTGC 420 TTTCTTTCTC AAAGTACTGT TTTATGTATG TTAAAGAATA TATACAGTCG GGCTGGGCAA 480 GGTGGCTCAT GCCTGTAATC CCAGCACTTT GGGAGGCTGA GGCAGGCAGA TCACCTGAGG 540 TCAGGAAAAA AAGAAAAAAA GACTTGATTA CTATGTATAT AGTATTTTTT TGTATACCTA 600 CATACCCATG ATAAAGTTTA ATTTATAAAT TAGGCACAGT AAGAGATTAA CAACAATAAC 660 TAACAATGAA ATAGAACAAT TATAATAACC TACTGTAATA AAAGTTAAGT GAATGTGGTC 720 TATCTCTCTC TCAAAATATC TTATTATACT TTATTCACCC TTCGTATGAT CATGTGAGAT 780 GATAAAATGC CAGCATCACT ACTCGTGCCC TTTGGGGCCA TTATCAATGA AAACAGGAGT 840 ACTTGAACAC AAGCACTGTG ACACCGTGAG AGCCGATCAG AGATGGCTGC TGAGTGACTA 900 ATGGGGCAGG TAGCATAGAA AATGTGGATA CGCTGGACAA AGGGATGATT CACATCCTAA 960 GCAGGATGGA GCAAGCTAGC AAGAGATTGC ATCATGCTCC TCAGAATGGT GCACAGTTTA 1020 AAACTTATGA ATTGTTTACT TCTGGAATTT TCCATTTCAT ATTTTTGGGC CACAGTTGAC 1080 CATGAGTAAC TGCAACCACA GAAAATAAAG CCTTGGGTAA GGAGGGGCTG CCGTATCATA 1140 CTCTGCCCCT ATACGGCTCT GCCACCACCC TCTCAGCTAA TGATGTCAGA AGTTATACCT 1200 TTATACATTG GGTGCCAAAA AACATAGACT TATTACTGGC TTTTTACTAT TAGTCTTTTA 1260 AATCATGTAT AAAAGGAAAA GTGGTGTTAC AACCCAAAAT GACAATAATA CTAGCTTTTG 1320 TAATTGTCCA TGTATTTACC TTTATAGAAG ATCTTTATTT CTTCATAGGA CTTTGAGTTA 1380 TTGTCTAGTG TTCTTTAGTT TATTTTTTTT TAATTTTTGC TTTCTTCCTT CTGCCTATAT 1440 AATGGCAAAT ATCCTTTAAT TTCAATCTGC AGAAGTCCCT TTAGCATTTT CTGTAAGACA 1500 GATCTAGTGG TAATAAACTC TTTCTGCTTT TGTTTATCTG GGAATACCTT CATTTCTTCT 1560 TTTCTGAGGG CAGTTTTGCC AGGTATAGGA TTACTTTTGT TTTGTTTTGT CTTCTTTTTT 1620 AAGAGACAGA GTCTCACTCT GTCAGCCAGG ATGGAGTGTA GTGGTGTGAC CATAGCTCAC 1680 TGCATCCTCA AACTCCTTAG CTCAAGTGAT CATCCCTGCC TCAGCCTCCT AAGAAGCTGC 1740 AACTACAGTT GTGCACCAAC ATGCCTGGCT AATTAAAAAA AAATTTTGGG GGGGGATGAG 1800 GTCTTGTTAT GTTGCCCAGG CTGGTCTTGA ACTCCTGACC TCAAGTGATT CTCCCACCTC 1860 AAGCCTCCTA AGTAGCTAGA ATTACAGGAA GGAGCTAACT TGTCCAGCAG GATTCTTGAT 1920 TGACAGTTTT TTCTTTTATC TCTTCAAATG TACCAACACA TTGCCTTCTT GCTGCCAACG 1980 TTTCTGCTGA GAAATCTGCT GTTAATCTTA CTGGAGATCC CTTATATGTA ACAATTTGTT 2040 TCTCTCTCCC TGCTTTCAAG ATTCTCTCTT GGCTCACACC TGTGGCTGGG TGCAGTGGCT 2100 CACACCTGCA ATCCCCATAC TTTGGGAGGC CAAGGCAGGA GGATTGCTTG AGTCCAGGAG 2160 TTTGGGACCA GCCTGGGCAA CATAACAAGA TCCTATCTCT ATAAGATTAA TTAGTTAGTT 2220 AATTAATCTA 2230
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