Tag | Content |
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EnhancerAtlas ID | HS095-09569 |
Organism | Homo sapiens |
Tissue/cell | HMEC |
Coordinate | chr14:102896390-102897550 |
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 | chr14:102897355-102897376 | TTTTACTTTTTTTTTTTTTTT | + | 6.16 | KLF4 | MA0039.3 | chr14:102897513-102897524 | CCACACCCTGC | + | 6.62 | NFAT5 | MA0606.1 | chr14:102897152-102897162 | AATGGAAAAT | - | 6.02 | NFATC1 | MA0624.1 | chr14:102897152-102897162 | AATGGAAAAT | - | 6.02 | NFATC3 | MA0625.1 | chr14:102897152-102897162 | AATGGAAAAT | - | 6.02 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr14 | 102896630 | 102896684 | chr14 | 102896752 | 102897202 |
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Enhancer Sequence | CCTCCTGGGT TCAAACGATT CTCCTGCCTT AGCCTCCCGA ATAGCTGGGA TTACAGGTGT 60 GCACCACCAC ACCAGGCTAA TATTTTGTAT TTTAGTAGAA AGGGGGTTTC ACCATGCACC 120 ATGTTACCCA GGCTGGTCTC GAACTCCTGA GCTCAGGCAG TCCTCCCACC TTAGCCTCCC 180 AAAGTGATGG GATTACAGGC ATGAGCCACC GCGCCCAGCC TAAATTTTGT TCAATTTTGA 240 TCAATTTGAA TTTCAATACT TACAAGTAGC TGGTGGCTGC CTATTGGACA GGGAGCTCTA 300 GGCAAGATCT GCCATTAAGT TATGTAATCT TCAGCAAGTC GCTTCACAGC AGAGTCCTCC 360 CCTCCAGTCT CCAGTGTACA CTTCATTGCC TGCAGTCTGC CCCTAACACA TGCCCTCAAT 420 AGAATGTGGG TGCTTCAAGG GCAGGAATTC CTGTGTCTTA TGGACTGCCA TGTCCCAGCA 480 GCTAGCCCTG TGTCTGGCAC ACGGAGGATC CCCGATAAAG AGAGGATGGC GAATGGATCA 540 AAGTGGGCTG TGGTCTTGTG TTGAGGGTAC TGTAGCTGGA ACTGCTCTGG CCTTGTGCCC 600 TGTGGTGTCG TGTTGCAGAA AAGATGAGTC CACTGCAGTG GGAAGCTCAC TGGCCCTTGG 660 GCTTGGGGAC AGGAGACAGG TACTCACATG CCTGTTCTCA CTCTGCGGTC TACTGGCCTT 720 GATGCTGTGT GGTAATGGAC TTCTCTGTCT TGAGTTTGTT CTAATGGAAA ATTACCTTTC 780 CCTCTTCCAG GAAACTTAAT TACAGGTACA CATGTATTTT TCAAATGCCC TTTGAGTAAT 840 CTTAAAGTAT ATTCAAGGCA GAGTCTTAGT ATGAAGTATA ACTAAGCTGT TTTGTTATAC 900 ACAGGCATCT CTCATTTGTA AATAATTTGT AAATTGAAGC GAGAAATGCT GTATTCTTAG 960 TATTTTTTTA CTTTTTTTTT TTTTTTTTTG AGACAGGTTT CACTCTGTCG TGCAGGCTGG 1020 AGTGCAGTGG CATGATCTCA GCTCACTGCA ACCTCCACCT CCCAGGCTCA AATGATTCTC 1080 CCACCTCAGC CTCCCAAGTA GCTGGGACTA TGGGCGTGCA CCACCACACC CTGCTAAATT 1140 TTGAGACTCC GTCTCAAAAA 1160
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