Tag | Content |
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EnhancerAtlas ID | HS105-34752 |
Organism | Homo sapiens |
Tissue/cell | IMR90 |
Coordinate | chr17:48597150-48598470 |
Target genes | Number: 23 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Foxd3 | MA0041.1 | chr17:48597891-48597903 | AAACAAACAAAC | - | 6.32 | Foxd3 | MA0041.1 | chr17:48597895-48597907 | AAACAAACAAAC | - | 6.32 | Nr2f6(var.2) | MA0728.1 | chr17:48597649-48597664 | GAGGTCAGAAGTTCA | + | 6.38 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr17 | 48598016 | 48598222 | chr17 | 48598288 | 48598354 |
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| Number: 1 | ID | Chromosome | Start | End |
GH17I050517 | chr17 | 48594653 | 48597496 |
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Enhancer Sequence | GAGGCGCAGG GCTGTAAGCC AGCTAGCATC TTGTGCCTGG CCCGGAGGCA GGGTAGTGTG 60 GAAGTGGCCA GCATAGCTCT ACAGTGAAAC AGGCCCAGGG CCTGTTTCTC TGTGGTTCTC 120 TGGGGTCTTA GGCAAGTCCC AGAGTCTTCC TGAAGTCCGG CTCCCTCTTC TTTTTCTTCA 180 GTAAAACGGT GAGAGAGCTA GGAAACTGGA GTGCAGCCAT AGAGCTGCCG TCCAGTGTGG 240 AGCCTTGAGC CACATGCCGC TGGTGAGCGC CTGGATCGTG GCTGCCCTGC CTTGAGAAGT 300 GCTGTCACTG TCAACTGGAC ACTGGCTTTA GTGTGAAAAC AATATATTTT ATTAATCATT 360 TTTATATTGA TTACATGTCA AAATGACAAT ATTTTTGATA TACTGAATTA AATAAACTAT 420 ATTACTAAAA TGAGGGCGGG CACAGTGGCT CATGCCTATA ATCCCAGCAC TTTGGGAGGC 480 TACGGCGGAT AGATCACTTG AGGTCAGAAG TTCAAAACCA GCCTGGCCAA CATGGTGAAA 540 CCCTGTCTCT ACTAAAAATG CAAAAATTAG CTGGGCATGG TGGTGCGCGC CTAGAATCCC 600 AGCTACTTGG GAGGCTGAGG CAGGAGAATT GCTTGAATCT GGGAGGTGGA GGTTGCAGTG 660 AGCCAAGATC ATGCCATTGC ACTCCAGCCT GGGCAACAAG AGCAAAACTC TGTCTTAAAA 720 TAAATAAATA AATAAATAAA TAAACAAACA AACAAACTAT ATTACTAAAA TGAATCCCAC 780 CTGTTTCTTT TTTCCTTTTT CAGTGTGGCA TCTAGAAAAC TTTCAGTGAC ACGTGTGGCT 840 TGTGCTTGTG GTTTGCATTC TGTTTCTCTT AAGCAGCACT GCTTTAGAGC CTGCCAGGCT 900 GCCTGGGTTC AGGTCCCAGC TGTGTCGTGT TAGTGAACCC CAGAGTGGTT GAACCCCTCT 960 GGCCTGTAGT TTCCTCATCT GTAAAATATG CACAGGGTTG TGATAGGGCT AAATGAGATA 1020 TGAAATGTAT TAAGAGGTTC TGGCTCATTG TTAAGCACTC AATAAAAGGT AGCTGCTGTT 1080 ATTATTTTTA TTATAATCCA AAGATTTGGC TATTTGGAAG CTAATTTTTC AGGAGTCTTG 1140 TGTAGGGCTG CTGAGGAGGT ATAGGACAGG AGAACGGGAG TCTAGCTGCC ACAGGGAAGC 1200 TGTATTTTTA GTCCTTCCTA GAAATGGTGT TGGGATAGGC ACTCTCAGAG CCCTTGAGAA 1260 GTGGGTGAGC AAGGGGACAT GGCAGCAGCC TGTGCTGAGG GTCCTTGGAC CTCATGCTAG 1320
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