Tag | Content |
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EnhancerAtlas ID | HS108-42435 |
Organism | Homo sapiens |
Tissue/cell | K562 |
Coordinate | chrX:49138880-49139830 |
Target genes | Number: 29 | 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) |
RREB1 | MA0073.1 | chrX:49138940-49138960 | TGTGTGTGTGTGTGTTGTGG | - | 6.71 |
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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: 1 | ID | Chromosome | Start | End |
GH0XI049282 | chrX | 49139061 | 49139619 |
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Enhancer Sequence | AGGAATAGGG AGTGGGTGAG AGACTCTGTG TGTGTGTGTG TGTGTGTGTG TGTGTGTGTG 60 TGTGTGTGTG TGTGTTGTGG GCGGGGGTCG GTTGCAACTT TAGATTGGGT GGCCTGGGAA 120 GGCTTTAGTG ATTAGTGAGA TCTGAGCGAA GATCTGAGGA AGGTGAGAGA GTGAGCCACG 180 TGGATAACTA AGGGAAGAAC ATCCCAGGCG AGTGTGAAGT TCCTGAGGTG AGGCCATGAC 240 TAACGTGTGT GAGGGACAGT GTAGAAGCCA GCGCAGCAGG GGCAGAACGA GGGAGGGGGA 300 GAGTGGTGCG GGGTGAGGGA GAGAGGTGGC TGAGGACAGA TTGGGTGGTG CCTCACAGGC 360 CATGGTGAAG ACTTTGGCTT TTACTCCGAG TGAGGGGGAG CCGCAAGAGC ATTGTGGACG 420 GAGGAGGGAT GTAATCTGAT TTAGGATTTA ACAGGCTCCC TCTGGCTGCT GCTTGGAAAA 480 TAGACGTCAG AGTAAGGGTG GAAACAGGCG ACTCGTGAAG GGGAGGCCAC TGCAGTGGTC 540 CAGGCGAGAG TGATGGTAGG TAGGGGAGGT AGAGACATTT TGGAGGGTGT GTGTGTGTGT 600 GTGTGTGTGT GTGTGAACTT TTTAATTACA AAAAGTTTCA AACATACAAA AGTAAAATAG 660 TATAATGAAC CTACGTACAC CATCCCCCAG CTTCAGTAAA TATCAACACG TGCTCATTCT 720 TATTTTATCT GTACCCCGTC TCCTCCCTCC CATTCCCTCT GGAATTATTT TGGAAGACAT 780 CCAGACATCA TCCCATCCAT AAATACTTCT GTTTGTATCT CAGAAAATTA AGAACTCTTT 840 TTTGTTTTTT TTTTTGAGAC AGAGTCTCAC TCTGTCACCT AGGCTGGAGT GCAGTGGTGT 900 GATCTCAGCT TACTGCAACC TCTGCCTCCT GGGTTCAAGC AAGTACATCC 950
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