Tag | Content |
---|
EnhancerAtlas ID | HS181-01807 | Organism | Homo sapiens | Tissue/cell | Sperm | Coordinate | chr10:51557800-51559530 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
SOX10 | MA0442.2 | chr10:51559469-51559480 | TCCTTTGTTTT | - | 6.32 | Sox3 | MA0514.1 | chr10:51559470-51559480 | CCTTTGTTTT | + | 6.02 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | TTTGAGACTG GCTCATTTCA CTTAGCATAA TATCCTCATG GTTCATCTGT GTTGACGCTT 60 GCATCAACAT TGCCTTCTTG TTCGAGGCTG AATCATGTTC TGTAATATGG AGAGACCACA 120 TTTTGCATCT CCATTCATCT GTTGATGAAC ACTTGGGTTG TTTTCCACCT CAATCTCATT 180 TCTTTTCTGT TGTTTTTGAA ACTTGATAAG TAGCTTTATT CCAGATGGGC TCCTGAAGAC 240 AGGAAAGAGT ATCTAATTGT CTGACACTAT TCCAGAGATT GGCCCGGTCA TCACCTCAGT 300 CTGGGCCTTG TAGATTTGTA GAAATAGCAG TGGCTCTGAG CATAGGCAGA GGGATCAGAT 360 GTGAGGGGTA AGGGAGGATC TGTAGTGTGC CTTGCACCAT AAAACTTATG CTGCTTCACT 420 GCTCAAGTTT AACTCACGTC AGCCCAAAGG CTATGCAGAT GTTTTCTGCT GGGTTGCTAT 480 GGACACCAGA AGTCTAGAAC TTGAGCAGGC GGAACACAGA GTACCCGCAG TGCCGTCCTA 540 ATTTACCTGT TTCCTCAGCA GCTATGTCCA TAACAGCTAC CTAACTCCCA ACCCCCCAAA 600 TCCATCTAAC CTCTTCATGT AGCCTTGGCT TGTAGTGTTC TGCAGGAACA GGAATGGATC 660 TGATGGCAGA GCATTGGTGT CAAGGGGCAT TTCGCAAACT TGTCTGATCA CAGACTCACC 720 TGGGAAGCTT GATGAAATAC AGATTCCTGG GCTCCATCCC AGAACTGATT GATCAGAATC 780 TGTAGGGGAG GGGCCAAGGA ATCTGAATTT TAACAGGTGC CTCGAGAGTC TTATGAGGAC 840 ACTGCGAGTA AAGAAGCAAG CACTTGACTT AGAGCAGAAC ACCTGAGTCC TACTGAACTT 900 GAAGTGCCTG GAGAGTTCCA GCCACATTTA TCGAGCAGGC CTCATGCTAG GTGCCTAATG 960 GAACAGAGGA ATATTGGACT GGGAGATGGC TGGCTGCTCA GAGCAGGCTC CTGGGCATCG 1020 CATTGGCCAG ATCACTGGGT ATTACAGCTG AACCTTGATT TTGTGGCTCC AGAAATTTGA 1080 CATTGTCTTT ATATCAAGTG TTGATGTCAC TCTGGTGGAG TGTGATTGTA TCCCAGCCAG 1140 GTGAAGGACT GGTGACTGGT CCCTCCCTCA CATAGGAGCG TGGCTCCCTG GTGGCTAAAA 1200 TGTCCATGTC ACCCAGATTT GGCATCCCTG CCCTCTTCTA AGATTCTCCA CTGTAGGCTG 1260 GGATTCTCGT GGTCCTGGTG TGGAAACGAG CCAGGCTGCT CCTTGCAGTG AAGAGGGAAG 1320 AACCTCACTG TTGGAGTCAG AGTAACTTGA GTCTGAATCT CCATTCCCTT GTATACTAGC 1380 TGTGTGACCC TGAGTCAGTT TCTGAATGTC TCTGAGCCTC TGTTTCCTCA CATTATAATT 1440 ATGTGGCTAT GATAATTAAA TGAGATTCTG TGTATATATT CTTTAACCCA ACAAACACTT 1500 AATGCCTTCT CTGTGCCAAT TCTGTGTCCT GTGATCCTGG GACAGTAACT GACACCTGGT 1560 CAGGTTTCAA GGTTTCAAGG TTTCTACTGC CATGTTGCCT GTTCCATTTG GCACACTGCT 1620 CCATGCAGGG GAAATGAATC AACACCTTCT TCCCTGGAAT TGCCTCACCT CCTTTGTTTT 1680 TCTCATGAAC TTTTTTCTCC TCCATGGAAA AATACAGACT TTGATTAAGC 1730
|
| |
|
|
|