Tag | Content |
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EnhancerAtlas ID | HS105-04668 |
Organism | Homo sapiens |
Tissue/cell | IMR90 |
Coordinate | chr1:145712990-145714830 |
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 | Gfi1b | MA0483.1 | chr1:145713053-145713064 | AAATCACAGCT | + | 6.14 | 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: 2 | Chromosome | Start | End |
chr1 | 145713047 | 145713169 | chr1 | 145713773 | 145714400 |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I145720 | chr1 | 145713284 | 145714909 |
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Enhancer Sequence | TTTCTAAAAT TTATTATTTG TACGAAGCAT ATAGAGGCTT GGAGGGGACT TGTGACTTGC 60 TTAAAATCAC AGCTCCTAAG TTGGGGAGCA GGACTCTAAC CCAAGTTATG AGAGTCTTTC 120 TCTTGGAGTC CCCTTTGTCC CTCTCCTCAC AGCCGCTCAT CCATTCACGA ACAGCTGTTA 180 ACACAAGAAC GACTGTACTA AGTAATAAGG TCATAAAGTG TCAAGGGGCA GCACAGGAGA 240 AATTCTGGAT GAGGGATGTG GAAAGGCTGC AAGATGGCAA TGAAGTTAGG CCTTCATAGT 300 TGTTTGTGGG CTCTGGGGAG CTGGTGACTA AAGAATACGG TGGGTGAATT AAGGTGGGGA 360 ATGGGCTGAG GAGATCTGGC TTCCAGTCCT GGCTCCGCAC TAGGTAGCTG TGGAATGTTG 420 ACAAGGTCGT GTCCCTTCTC TAGGCGTGTT TCCTAAGGGA CTGGTGCAGC GGGATGGGAG 480 GGGCGCAGGG TAGGGACCGC TTCCAAGGAG AGAGAGGACA GGCGGGAGGG GCTGATGCAG 540 CTGGTCACTC CGCTGGAGTG GCCAGACTTC GCGGTGCCTA GGGCCGAGTT GAAGAAGAGC 600 ATGTAAGTCT GTTGTGGGCC CCTCACCAGC GCTGGGGGGC AGCGAGGTCA CTGGGCAAGG 660 ATGCTCTGGG AAGTGACCTT GGTGCCCGGG AGGGGAGCAC CCTGTTGTGA TGCAGGCGGG 720 GCAGCGCGGA GCCGGCGGCG CTGATTTCGC ACTCTGGCCG CTAGAGGGCG CTGCCTTTCA 780 GCCAAAGCCG AGTGACCCCC TACCTGCCCC GCGTTGGCCC GCGTCACTCC AGCCATGGGC 840 CATCCAGCGA GCATGGGGGC TAGCCAGGGA AAGTCTAAAC TAGGAGGGGA GATGAGGGGG 900 TGCAAAGTTG GGCCTGGTGG GTCCTGGGGA CGCAGCATGT ACTAGAGCGG CACCTGGCCC 960 TCAACAGAGG GGAGAGCGGG TGGTCGTGAG AAGTCTGGGA ATTTTCCGGG CCCACTACAC 1020 GCCAGGGGCG GGTCTCCCCT CTTAAAACGT TGTGAGCCCC AGCGCGGGCA GGGGGGAGGG 1080 TGCCCGTGGA GTTGGCATCC TCATCTTTGA TGGTCCCCGG GGCTCCTGAG CTGCGCTGGT 1140 GGCCCCAGGG CTCGGTGCCT CTCTCAGGCG ACAGCTCACA GACGGCGGGA AACTCTTCCC 1200 TCCCGCACCT TCGGAGGCGG TCCTGGAGTC TTGTGGACTC CTGGGTTCAA ATCCAAGCTT 1260 TGTGTGACCA GCACATTGCT GGACCTCACT CAGCCTCACA TTCCTCTTGT GTTTAAAACT 1320 ACCTCATAGG AATGTGGTGA CGGTTAGATG ACACATAAAG CTTTGCCAGA GGTTTTCTGG 1380 GGAGGGTGGG GACAAGAGGG CAAGGAAGAG TCTCCATTTC CTCTGCCACC GGAGCCCGGA 1440 TCTAACCTCT CAGAGGAGCT GGAAGGTCAG CTCTGAGCTC CACAAATACC TCTGTATACA 1500 GATCTCCCAC GACACTGAAA AAGATGCCCA GAAAGATCTC ATTTGCAGCT GTGAAGGGGC 1560 TTCTTTTTCA ATCTCCACAA CCCCAACTGC CTTAAAGTAG AACCAGACTT GTTAGTAGAC 1620 AGAGGTTTGG GCTGGGGGGC CCTTGAAGCT CTTGTCTGAG ATCTCAGGCT TCCTGCTCAA 1680 CACACCAAAG CAGGTGCCTG ACATAAAGGC GCCATGGACC TCTTTGGTGG TCTGGGAAGG 1740 CATATGGAGT CCCTTCTCAG AACAACATTT AAAAATTAAT AAGATACATG GGATAATAAA 1800 GGGAACAAAT TATGACAAGA CAGTTGTCAA AACATTAGAA 1840
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