Tag | Content |
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EnhancerAtlas ID | HS187-26057 |
Organism | Homo sapiens |
Tissue/cell | Th1 |
Coordinate | chrX:153541220-153542250 |
Target genes | Number: 14 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
MEF2C | MA0497.1 | chrX:153541468-153541483 | TTTTATTTTTGGCTT | - | 6.38 | NFYA | MA0060.3 | chrX:153541503-153541514 | TCTGATTGGTC | - | 6.14 | NFYB | MA0502.1 | chrX:153541504-153541519 | CTGATTGGTCAATTG | - | 6.91 | NKX2-5 | MA0063.2 | chrX:153542063-153542073 | ACCACTTGAG | + | 6.02 | Nr2f6(var.2) | MA0728.1 | chrX:153541631-153541646 | TGACCTTTTGAACTT | - | 7.16 | RARA | MA0729.1 | chrX:153541628-153541646 | GGCTGACCTTTTGAACTT | - | 6.03 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chrX | 153541562 | 153541846 | chrX | 153541697 | 153541855 |
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| Number: 1 | ID | Chromosome | Start | End |
GH0XI154312 | chrX | 153540808 | 153542233 |
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Enhancer Sequence | GTCTCCATGG ACGAACCAAT TACTAGAGTG ACATGTAACT AACAGTTCGT AGGCAATAAA 60 GAGAGGTTTG CCATTTTTAA AAAATACATT TAGGGGTCCA AAGTGCAGCT GTGTCACGTG 120 GATAGATACT GTGTAGTGGT GAGGTCTGGG CTTTCAGTGC ACCCAGCATC GGAGTAGTGG 180 ACATTGCACC CAGTAGGTAC TTGATCTTTC ACCACTCCTG GCTCCCCTTC TCTTTTATTA 240 GGTCTGATTT TTATTTTTGG CTTTCACATG TGTGTCTGAA TTTTCTGATT GGTCAATTGC 300 TATTTATTAG CTCCTGGTGT GGTGTGCCTT TTTCTAGCTT CCTAACTTTG GTTTGTGCAT 360 GAAACTGCCA CGACTCTGTG TCTCCGCTAA GAAGACTGGC CCCAGGCGGG CTGACCTTTT 420 GAACTTACTC TCTGAATTAC ACAGAGGAGC AGGCCAATTC ATCAGAAACC TCAAAAAGGA 480 ATCAAATGAT GCACAAAACT CTTGAGTATC AAGTCCTTTT GGTTTTTAGC ACCTTTACAT 540 CCTGCCTTCT GGTATATCAT AGCAGACCTG ACATAGGCAA GTTCTTTATG GCCTAGAGGA 600 AGTAAGGCGG CGAGCCTAGG GAGGAAGGAC ACACTTTCTG ATCCTTCTTT ATTTGGAGAA 660 ATTTTGAGTG TTGCTCATGT TTTCTTAGCC TGGTAATGAG GGTTAAAAAT AAATGAATTT 720 TGAATACTTG AGAAATCAAA AGACAAAAAC CAGAAGAAAG GAGACGGTAT ATCAACAAAG 780 GGTGGGCAGG CACAGTGGCT CACTCCTGTA ATCCCAGCAC TATCAGGAGG CCAAGACAGG 840 AAGACCACTT GAGCCCAGGA GTTCAACACT AGCCTGGGCA AAGTAGTGAG ACCCCATCTC 900 TACATAGAAT TTAAAAATTA TCCAGGCATG GTGCCATAAT ATGGTTCCAG GTACTCTGGA 960 GGCTGAGGCA GGAGAATCAC CTGAGTCCAG GAGTTTGAGG GGATAGTGAG CTATGATTGG 1020 GCCACTGCAC 1030
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