Tag | Content |
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EnhancerAtlas ID | HS182-18730 |
Organism | Homo sapiens |
Tissue/cell | Spleen |
Coordinate | chr6:34925730-34927290 |
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) |
SOX10 | MA0442.2 | chr6:34925997-34926008 | AAAACAAAGCA | + | 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 |
GH06I034958 | chr6 | 34926178 | 34926977 |
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Enhancer Sequence | GCTTGTAAGA GTCAAGTATG GGTACCATGC ATGCAAATGC ATGTAAACAT TTAGACATTG 60 TCATTTCAAG TTATTTGGTG TGTAACCATG GTACAAACAA GGATGGGCTT TATATAACAT 120 AGGATTATGG GTTCCAGACC CTCATATCGA CCTACTGACC AGACATCTAC ATATGGGAGT 180 CAAAATTCAT TTCAGCCTCA ACAAATTCAA AATAAAACTC CCTCCCGCTC CCTTCTCTTC 240 TCCCCTACCT CACGTCACCA CAGTCACAAA ACAAAGCAAC CCTGGTTTTC CCCCAGAATT 300 CTCACTACTC ACTGAGTAGC CTGATTCAAA CAGCCGCCAG TGCACCCCAA CCTGCATTTG 360 ACAAGGTCCT GTCTTTTCTA TTGAATCTAT CCTTTTTTCT CTGTCCTCTT TACACTGCAT 420 GAAGGTGTTT ACTTCATGCC TGAATTACTA ACTTCACCTG GGCTCCCTGG ATCTAGTCAC 480 ACACTTCTCT TAGTGTATCA TTTACACACC TGCTCAGCAT AATGATGAAA AAAAATTCTG 540 AAATATGTCA GGCCATCACA ACAGTATAGT GAATAACAAA TGGACCATCT GAGTACCCGC 600 CTCCCAGCTG TCAACAGAAG GATTTTTCTA AAACACCCAT CTGATTATTC CCCGCTTGAA 660 TCTCTTCAGC GGCATACAGG ACCCTTTCTG ATTTGACTCT GCCGGCCTGT TCAACCTTGC 720 ATTCACCATC CTTCCACTTG TATGCTCCAG CCACTCGTAG TTACTTGCAG GTGTCCCACT 780 TTGCTGAGAC TACTCAGGGG ACAGTGAATT TGGATGTTGC CTCTTCGTTT CTGCCTGGCT 840 GCTTCCTTCT AAACTTTAAG GCTCAACTTA AGTATCTCCT CTTCTGTAAA ACCTCTCTGT 900 TCCTATTTCC CTTAAGCCAG TTTGTGTACT TCCTTCCCAG AATGTCACAC ACTGTACAGT 960 ATTGTCATTT GTTTACTGGT CTGACTTCCT CACTGAACTC AAGGGTGGGG ACTGTCCAGC 1020 GCTGTGGCAT CAACATTGAT TGGATTCAAC TGGATTGGAC ACTTCTGGCC CATTGAGATG 1080 CCATTACTTG TCTGTGTAAA GTAAGCAATA AAGTAGCTGG GCTACCACAT GAATCATGTT 1140 TACTGCCAGC TAAGGCCACT TAGGGTATCA TTCAGTCCAG AAATCTGACC TCACGCACAT 1200 GAAAGTGGCC TGAGCACTTT GGTTCTAACT TATGGTTCTT CTGTCGCTGT GTTTTATGTA 1260 CAGACATCTC AGATGCAGTG TTCTTGTATG TCCCATCAAG AGATTGTTGC CATTCTTAAT 1320 GGATATAAAT GTAGTAGGTT TGTTATACTG CATAGAGACC ATGTCATACT GGGGTAATGT 1380 TGGTTCAGGG TTGGCAAGAA TCTGATCTGG TAAGAGGGAA TGAGCAGATT GCTGAAAACT 1440 GAATGTTAGA AGTTGCACCC TGGTGGCCCT GGGCCAATTC CTTACATAGT GCTCTGTTCT 1500 TGGAAACATG AGGGATTTCC CTAAAGGACT TATAATATAT GGTATGAATA AGCAGGATAA 1560
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