Tag | Content |
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EnhancerAtlas ID | HS066-00327 |
Organism | Homo sapiens |
Tissue/cell | GM18516 |
Coordinate | chr1:110407140-110408310 |
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) |
Sox6 | MA0515.1 | chr1:110408271-110408281 | CCATTGTTTT | + | 6.02 | TBX2 | MA0688.1 | chr1:110407413-110407424 | TTTCACACCTC | - | 6.14 |
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| Number of super-enhancer constituents: 4 | ID | Coordinate | Tissue/cell |
SE_00603 | chr1:110407003-110408630 | Adipose_Nuclei | SE_04393 | chr1:110407035-110407839 | Brain_Anterior_Caudate | SE_53713 | chr1:110406458-110408779 | Spleen | SE_62091 | chr1:110406355-110450750 | Toledo |
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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 |
GH01I109863 | chr1 | 110406305 | 110408687 |
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Enhancer Sequence | TCTTGGTTTT GGCTGGCTTC TTTACCACAT CCTATTTTAT CAGCAGGGGT CTCTGTGACC 60 AGTATCTTGT AAACCAGTCC TGCCAAAGTC CTATCACACA AATAGTCCAG CTCCTGACGC 120 GAGCTGCATT GAGTCCTCCT GCAGTGTCAT GCTTAGACAA GAGTGTACCA CATGTGGGCT 180 GCTACACACA GACACCCCTC TGGTGAAGCA GCTGGGCTTT CTGGGTGTGT CAGCCTCAGC 240 CATGCACCAT GCCAGAGGAC AATCAAGCCA TCGTTTCACA CCTCCTCTTC CACTTGGGTG 300 GGTGCAGTGG GTGTGAGCGG TGGTTCTTGG TCATTTCAGG TGGAACCCAT CCATGGATTC 360 AGGTACGATC ATTTCAGCCC ATCAGAGTTA CCTTTTGCCT CAAATAAGAA GGGAGTGGTT 420 CAGATCCGTC TTCTCCCAGA AGGCTCCTTG TGCTCCTGTA TACATTTGTC CAAATGCTTC 480 AGCAACCAGC TCTTCATACC AAGAAATATA GAGAACAGCC TTTGTCAAGC CACACAGTAG 540 GGAAAAAATG TCCAGTTATA TCCTCTTCTC AGGATGATGG GTGCCTAGCT GCCCACATTT 600 ACGTAACTGA AGGAGACCAT TCACACGATT GTTCTAAGAA CAAAGACTTC CTCTAAGAAG 660 ATTGGCTGCC TCCTCTTGCT AGCTGGCAAC TTTTAAGTGG CAGTTCATTG AGGCAGAAAG 720 ATGTAAAATT CCACTTTCTA GGCACTCCAT TACAAATCTA GTTCACACTT GTACCATGAA 780 TTAATGTTGT TTGGAAGTCA GAGGTCGTTA AATTTACCCC ATTTAGACAT TCCTCCGTTT 840 TGAAAACTGA CAAACATTTC ACACTTCCCT GGCTGTTGGC TCCTTTCCCA AATTTCTCAG 900 AAATCACGGA CAGTAGTTCT GCAATCACAT CCCCGAGTTC CGAGGAGATT CCTCTAAAAC 960 CAGAACTCGA ATGTGGCCAG ATGCTTCCAC CACCTCCTCA TGGCTGCGCT CCACGTTCTT 1020 CTGGAATTTG CCTTTACACT TTCCGGTTTG AGAATTACTC TTCTTGAGGG AGAAAAACAT 1080 TATGCATGAA AAAATTTGTC CCCTCCACTA AGTGTGGGGC CTGGATCTTC CCCATTGTTT 1140 TTCTTGCTTC AGATACTTTT CTAAAACAGG 1170
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