Tag | Content |
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EnhancerAtlas ID | HS003-02162 |
Organism | Homo sapiens |
Tissue/cell | A549 |
Coordinate | chr1:145712940-145715260 |
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 | CTACCTGCAA GACTGTGTTT AGTCCTTATA AAACACTAAG CCATTATTAT TTTCTAAAAT 60 TTATTATTTG TACGAAGCAT ATAGAGGCTT GGAGGGGACT TGTGACTTGC TTAAAATCAC 120 AGCTCCTAAG TTGGGGAGCA GGACTCTAAC CCAAGTTATG AGAGTCTTTC TCTTGGAGTC 180 CCCTTTGTCC CTCTCCTCAC AGCCGCTCAT CCATTCACGA ACAGCTGTTA ACACAAGAAC 240 GACTGTACTA AGTAATAAGG TCATAAAGTG TCAAGGGGCA GCACAGGAGA AATTCTGGAT 300 GAGGGATGTG GAAAGGCTGC AAGATGGCAA TGAAGTTAGG CCTTCATAGT TGTTTGTGGG 360 CTCTGGGGAG CTGGTGACTA AAGAATACGG TGGGTGAATT AAGGTGGGGA ATGGGCTGAG 420 GAGATCTGGC TTCCAGTCCT GGCTCCGCAC TAGGTAGCTG TGGAATGTTG ACAAGGTCGT 480 GTCCCTTCTC TAGGCGTGTT TCCTAAGGGA CTGGTGCAGC GGGATGGGAG GGGCGCAGGG 540 TAGGGACCGC TTCCAAGGAG AGAGAGGACA GGCGGGAGGG GCTGATGCAG CTGGTCACTC 600 CGCTGGAGTG GCCAGACTTC GCGGTGCCTA GGGCCGAGTT GAAGAAGAGC ATGTAAGTCT 660 GTTGTGGGCC CCTCACCAGC GCTGGGGGGC AGCGAGGTCA CTGGGCAAGG ATGCTCTGGG 720 AAGTGACCTT GGTGCCCGGG AGGGGAGCAC CCTGTTGTGA TGCAGGCGGG GCAGCGCGGA 780 GCCGGCGGCG CTGATTTCGC ACTCTGGCCG CTAGAGGGCG CTGCCTTTCA GCCAAAGCCG 840 AGTGACCCCC TACCTGCCCC GCGTTGGCCC GCGTCACTCC AGCCATGGGC CATCCAGCGA 900 GCATGGGGGC TAGCCAGGGA AAGTCTAAAC TAGGAGGGGA GATGAGGGGG TGCAAAGTTG 960 GGCCTGGTGG GTCCTGGGGA CGCAGCATGT ACTAGAGCGG CACCTGGCCC TCAACAGAGG 1020 GGAGAGCGGG TGGTCGTGAG AAGTCTGGGA ATTTTCCGGG CCCACTACAC GCCAGGGGCG 1080 GGTCTCCCCT CTTAAAACGT TGTGAGCCCC AGCGCGGGCA GGGGGGAGGG TGCCCGTGGA 1140 GTTGGCATCC TCATCTTTGA TGGTCCCCGG GGCTCCTGAG CTGCGCTGGT GGCCCCAGGG 1200 CTCGGTGCCT CTCTCAGGCG ACAGCTCACA GACGGCGGGA AACTCTTCCC TCCCGCACCT 1260 TCGGAGGCGG TCCTGGAGTC TTGTGGACTC CTGGGTTCAA ATCCAAGCTT TGTGTGACCA 1320 GCACATTGCT GGACCTCACT CAGCCTCACA TTCCTCTTGT GTTTAAAACT ACCTCATAGG 1380 AATGTGGTGA CGGTTAGATG ACACATAAAG CTTTGCCAGA GGTTTTCTGG GGAGGGTGGG 1440 GACAAGAGGG CAAGGAAGAG TCTCCATTTC CTCTGCCACC GGAGCCCGGA TCTAACCTCT 1500 CAGAGGAGCT GGAAGGTCAG CTCTGAGCTC CACAAATACC TCTGTATACA GATCTCCCAC 1560 GACACTGAAA AAGATGCCCA GAAAGATCTC ATTTGCAGCT GTGAAGGGGC TTCTTTTTCA 1620 ATCTCCACAA CCCCAACTGC CTTAAAGTAG AACCAGACTT GTTAGTAGAC AGAGGTTTGG 1680 GCTGGGGGGC CCTTGAAGCT CTTGTCTGAG ATCTCAGGCT TCCTGCTCAA CACACCAAAG 1740 CAGGTGCCTG ACATAAAGGC GCCATGGACC TCTTTGGTGG TCTGGGAAGG CATATGGAGT 1800 CCCTTCTCAG AACAACATTT AAAAATTAAT AAGATACATG GGATAATAAA GGGAACAAAT 1860 TATGACAAGA CAGTTGTCAA AACATTAGAA GAATGTGTGG TAGAGCAGTA CACATGCTTC 1920 TTTAGATTTG ACATCAGCCT AATAACTGTT GTAATTCTGT AGTAGTGCTG AGCGTTAAGG 1980 ACATTTGGAG AAATCTATAA AAACTGTAAT GAGATTTGAA AATATTTGTG TTTTCTATTG 2040 ATGGCAAATT CTATTGTGGT TCATTGTCTA CATTCATAAC TGAAGCAAGT GCTGACTTTC 2100 AATTAAAGAT TAGTGAAAAT AAAGATGTAT TTTTCCCCCC AATTCACAAA TCCCATGAAT 2160 AAATCTATTC ACGGACCTCC AAGAGGTCCA TGACGTGAAC CACCTAGGAC ATGAACTTCC 2220 CCCGGAGGTG CCTCACAGGG CCAGCTCCAA GCCCCGTGGC ACCTCCCGGC TTGTCTCAGG 2280 CCAATCCTTG AAGAGCTCCA GCAGATCTAA ACTTTGGTAA 2320
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