Tag | Content |
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EnhancerAtlas ID | HS069-00485 |
Organism | Homo sapiens |
Tissue/cell | GM18951 |
Coordinate | chr1:145713070-145714860 |
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) |
CTCF | MA0139.1 | chr1:145713744-145713763 | TGGCCGCTAGAGGGCGCTG | + | 7.3 | MSC | MA0665.1 | chr1:145713159-145713169 | AACAGCTGTT | + | 6.02 | MSC | MA0665.1 | chr1:145713159-145713169 | AACAGCTGTT | - | 6.02 | MYF6 | MA0667.1 | chr1:145713159-145713169 | AACAGCTGTT | + | 6.02 | MYF6 | MA0667.1 | chr1:145713159-145713169 | AACAGCTGTT | - | 6.02 |
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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 |
GH01I145720 | chr1 | 145713284 | 145714909 |
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Enhancer Sequence | TTGGGGAGCA GGACTCTAAC CCAAGTTATG AGAGTCTTTC TCTTGGAGTC CCCTTTGTCC 60 CTCTCCTCAC AGCCGCTCAT CCATTCACGA ACAGCTGTTA ACACAAGAAC GACTGTACTA 120 AGTAATAAGG TCATAAAGTG TCAAGGGGCA GCACAGGAGA AATTCTGGAT GAGGGATGTG 180 GAAAGGCTGC AAGATGGCAA TGAAGTTAGG CCTTCATAGT TGTTTGTGGG CTCTGGGGAG 240 CTGGTGACTA AAGAATACGG TGGGTGAATT AAGGTGGGGA ATGGGCTGAG GAGATCTGGC 300 TTCCAGTCCT GGCTCCGCAC TAGGTAGCTG TGGAATGTTG ACAAGGTCGT GTCCCTTCTC 360 TAGGCGTGTT TCCTAAGGGA CTGGTGCAGC GGGATGGGAG GGGCGCAGGG TAGGGACCGC 420 TTCCAAGGAG AGAGAGGACA GGCGGGAGGG GCTGATGCAG CTGGTCACTC CGCTGGAGTG 480 GCCAGACTTC GCGGTGCCTA GGGCCGAGTT GAAGAAGAGC ATGTAAGTCT GTTGTGGGCC 540 CCTCACCAGC GCTGGGGGGC AGCGAGGTCA CTGGGCAAGG ATGCTCTGGG AAGTGACCTT 600 GGTGCCCGGG AGGGGAGCAC CCTGTTGTGA TGCAGGCGGG GCAGCGCGGA GCCGGCGGCG 660 CTGATTTCGC ACTCTGGCCG CTAGAGGGCG CTGCCTTTCA GCCAAAGCCG AGTGACCCCC 720 TACCTGCCCC GCGTTGGCCC GCGTCACTCC AGCCATGGGC CATCCAGCGA GCATGGGGGC 780 TAGCCAGGGA AAGTCTAAAC TAGGAGGGGA GATGAGGGGG TGCAAAGTTG GGCCTGGTGG 840 GTCCTGGGGA CGCAGCATGT ACTAGAGCGG CACCTGGCCC TCAACAGAGG GGAGAGCGGG 900 TGGTCGTGAG AAGTCTGGGA ATTTTCCGGG CCCACTACAC GCCAGGGGCG GGTCTCCCCT 960 CTTAAAACGT TGTGAGCCCC AGCGCGGGCA GGGGGGAGGG TGCCCGTGGA GTTGGCATCC 1020 TCATCTTTGA TGGTCCCCGG GGCTCCTGAG CTGCGCTGGT GGCCCCAGGG CTCGGTGCCT 1080 CTCTCAGGCG ACAGCTCACA GACGGCGGGA AACTCTTCCC TCCCGCACCT TCGGAGGCGG 1140 TCCTGGAGTC TTGTGGACTC CTGGGTTCAA ATCCAAGCTT TGTGTGACCA GCACATTGCT 1200 GGACCTCACT CAGCCTCACA TTCCTCTTGT GTTTAAAACT ACCTCATAGG AATGTGGTGA 1260 CGGTTAGATG ACACATAAAG CTTTGCCAGA GGTTTTCTGG GGAGGGTGGG GACAAGAGGG 1320 CAAGGAAGAG TCTCCATTTC CTCTGCCACC GGAGCCCGGA TCTAACCTCT CAGAGGAGCT 1380 GGAAGGTCAG CTCTGAGCTC CACAAATACC TCTGTATACA GATCTCCCAC GACACTGAAA 1440 AAGATGCCCA GAAAGATCTC ATTTGCAGCT GTGAAGGGGC TTCTTTTTCA ATCTCCACAA 1500 CCCCAACTGC CTTAAAGTAG AACCAGACTT GTTAGTAGAC AGAGGTTTGG GCTGGGGGGC 1560 CCTTGAAGCT CTTGTCTGAG ATCTCAGGCT TCCTGCTCAA CACACCAAAG CAGGTGCCTG 1620 ACATAAAGGC GCCATGGACC TCTTTGGTGG TCTGGGAAGG CATATGGAGT CCCTTCTCAG 1680 AACAACATTT AAAAATTAAT AAGATACATG GGATAATAAA GGGAACAAAT TATGACAAGA 1740 CAGTTGTCAA AACATTAGAA GAATGTGTGG TAGAGCAGTA CACATGCTTC 1790
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