Tag | Content |
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EnhancerAtlas ID | HS098-16241 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr13:80706820-80708230 |
SNPs | Number: 2 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Mafb | MA0117.2 | chr13:80707578-80707590 | AGTCAGCATTAT | - | 6.14 | POU2F2 | MA0507.1 | chr13:80707903-80707916 | CTCATTTGCATTT | + | 6.28 |
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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 |
GH13I080130 | chr13 | 80704537 | 80709218 |
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Enhancer Sequence | TTTTTTTTTC CTACTCTAAA ACAGTGTTTG TACTTTTTTC TGGACTCCAA GTTGGATGCC 60 TTCACCAAAG TGGTTTCAAA GACTGGAACA AAAAAGCCTC CATCGAGGCC CTGGCTAGCA 120 CAGTCCCTGT TACTTTAAGA GTAGCATTCC ACCTCCCCCT CACACCCACA TACTTGTCCT 180 CTCTTTGCAC AGCAAGTGCC AAGCAGTGAC ATCTACTATA GTTTCTAGGA CACGATGGTC 240 TCTGCTCTAC AGGGAAAAAG AGCGAGCGGG ACAGAAAGAA GGCGGGTGGT GAGGGAGAAG 300 GAGCACAAGC CCAGCTATGT TCCCAGAGGA GGAGTCACTT CCTCGCAATA ATCCTGAGAT 360 GCTGTTTATG GCTGTTCTGC TGATATGAAG CCTGGAGCCG CAGGATGCAG CCTCCCCCTG 420 GCTGTCCATT AATCACGAGG GGCTGTTACA GAGTGTACAG AGTGGGAGTT CTGCCTACAA 480 GTGGCCTCTA ACTGTCTCCA GCTCAATGAA ATGAACCTGT GTGAAAACTT GTTTTATGAG 540 AGATTGGTTT ATTTGTAACT AAACTACTTC CTCTGTTATT TGATAAGATC AAATATTTGC 600 TACTGATAAT CTGAGAGTGT CACATTTATT ATCCTGTTTC AGCCGTTGCC TAACTCCTTT 660 GGAACTGACT CCGTTAACTC TTTGAGGGAC AGCAGTAGGT TTTAGAGGAC CGGTTTCTAT 720 TTTCTTTCAG CAAAGCCAAT GCTATCTTTC AGACACTGAG TCAGCATTAT TTTAGAACAG 780 CTATGACATG TGAATCAAAA AGAAGCCTTT CTCTTCCAAA ACAGAAAGCA GACAACCATA 840 GTAACAGGAG GCTCTGATAA ATTCCCTGGA GGTTCTGAAG CCACCATGAA AAGGAAGGAA 900 AGGTATTCTG ACTTACTAAT ATAAAAATGG TTTTGCACGT GCTAGGATTT CTGAAATCAC 960 ACATTTTCAA TATGTTCAGG ATGACTTTCT ATAGTTTGTT AGACCCTCAA ATATCTATGT 1020 GGGGCATGAT CTCTAAATCC GGCAGCATTC TGCATCTTGA CACTTGGCCT TTTGGAGTCT 1080 GAGCTCATTT GCATTTGGCA GGACTTGATT TCCTGCTTTG ACAGAACGGC GGTAAGGTGG 1140 TGGTGAAAGC CTTTACAGTG CTCCCTCGAA GGGCTCAAAG GACTTTCTGG ATATATAAAA 1200 TTATGTTTCC AAGAATTAAA TGGACCAGAA TGAGGCAGAT TTTGTTTGAA ACCAGGCTCT 1260 GTTACATGCA ACACATCTGA AAAACTTACT TACACTGAAG CATCTCTCTT GACAGACTCA 1320 TACTGGGACT GTTTTTCAGT TCTCTCACTC TCCAATCAGC TACACAGAGC TCTCAGTGAA 1380 TGTAGAAGAG GCTAAGGAAA TAACCACTTA 1410
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