Tag | Content |
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EnhancerAtlas ID | HS179-13137 |
Organism | Homo sapiens |
Tissue/cell | SkMC |
Coordinate | chr15:49188790-49190310 |
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) |
Klf1 | MA0493.1 | chr15:49189132-49189143 | AGCCACACCCT | + | 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 |
GH15I048896 | chr15 | 49188712 | 49190898 |
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Enhancer Sequence | ACAGACATGA GCCACCGCGC CCAGCCTGTA CAAACTTTTC TATTCCATTT AAGAAGGTCC 60 ACTCCTCACC CCAAAGCTCC CCAAAACATT CTGTGGACCT CTTAGAAATT ACAGATCCCA 120 GGTTAAGAAA TACTGCTTTA AATTAACCTC TCAAATTCTG CTGGCCTTGC TGATAGCAGC 180 GTTAACAAAT CTCCTGAAAT CCCAGCAAGG ACAGGCAGAT AGATGCCTAC ATTTTGTTGC 240 TTTTGTTCAC AAAGATCTTT TCTTCCCCTG CTACTGGGAC CAAGACATTA ACTGTAACAT 300 TTTCAAGAAC AAATAGTACT TTCAGTGCTT TTCTGGAGTC TCAGCCACAC CCTTGGGCCA 360 ACTTTACAAA TGCCGAGGAG AAAGAAAAAG AAAACAGAGT TGAGAGCGAT TTCTCCTGGG 420 GCTCAGGGGG TCCCCGCCAT TCTTGCAGCC CAAGCAGCTG CGCTCCTGCA GAACCTTTTT 480 GGAGCTGAGT GGCGGTGAGA CTTTCTCCAG CTAGCAAACA TTCAGCAAGT GTCTGCTCTT 540 AGAGGAGCAG AAATTTTGGG GTTTCAGTGG CTAAAGATTT CCATCCTGGG AGCCTGTATT 600 AGAAAGAAAG AGAAACGCCC CAGAGCACCA ACAGTGGCCA CTTTGTTTAT TGTTTCGCCA 660 CATGAGAGAG AAGGGGAGAA GTGGGCTGAT GTAAGAGAAT GAGAATGCCG TGGAAGATTT 720 GCTTTTAAGC ATATAAAACC CTGCCTACGC CATAAGACCA AAAAAAGATA TTTTGTCTGT 780 CTTAACAGAG TCCAAACTAA TCATCCAAAC AAAGCCACCT TTCTTCATCA ACTCCTGGCC 840 ACTACAACAC TTAAGTTATA ATTCTTCTGT GTTTTTAACC CTTAAACAGT TAAGCTCCTC 900 TGGAAGCAAT GTCGCCACAC ACACACACAC ACACACACAC GCACACACTT TTTTTTTTTT 960 TAAGTTTGGA AGGCAATATC ACAATCCAAG ACAAAGGGGA GCATTTAATG GGAGGAGAGG 1020 CTGCGCGGCA GATTTTTTCT GGTGAATGTC AAGATGCAGT TCTTCAGTAA ATAGGAAAGC 1080 CAGAAAATGT GCAACATGAA ACCAGGCAAA GGGGCCCAGC TGGAATGATT AAAGGCAATG 1140 ATCCCCACAT CCCCCACCTT CTGACACACA CACACACACA CACACACACA CATCTATAGT 1200 CACATATGCA GTGAAGGAGT AGTTCCAGTT TTGTCCCTGC AAATAGGAAT GAGAATAAAA 1260 TTTTAATCAC AGCAAGAGCC TTTCCAAAAT AAAAAGTCAA CGATACTCAG CCAAAACAAA 1320 TTCACCTGCG TTTCCCAAAG GTCTTTCTTT CACTTTGCAT CTCCAACGTA AGTCCTTAAA 1380 GAAATCAGTT AACAAAGTCT AAGGGACATG TTGCACCCTA AATGTCTTGG ATTGCCTTCT 1440 TATTATGAAT GAAGAGACTG AGTAATTCAG ACTGCACATC CATGTGGTAT CATGCTGTTC 1500 TCATTGTTCT AGGGAAACCA 1520
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