Tag | Content |
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EnhancerAtlas ID | HS181-15417 |
Organism | Homo sapiens |
Tissue/cell | Sperm |
Coordinate | chr8:785820-787360 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
NR2C2 | MA0504.1 | chr8:786671-786686 | TGCCCTTTGACCCTG | - | 6.81 | Nr2f6 | MA0677.1 | chr8:786671-786685 | TGCCCTTTGACCCT | - | 6.43 | Rxra | MA0512.2 | chr8:786671-786685 | TGCCCTTTGACCCT | - | 6.41 |
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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 |
GH08I000836 | chr8 | 786605 | 786748 |
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Enhancer Sequence | AGCCGGTCTG TGGCACGTTC TTTCGTGTGG GTCCAGGCTC ACCGTCGCTG TCTCAGAACT 60 GCTTTCCTGT TACGCTGCCG TAACTGTGAT GTTTGTGTAT CCATCCCTTC ATGTATCAAA 120 CGCAGACCTT TTCTCACAGG TTTGGTCATT TTTGGGTGTA AGACACGTTC CTTCCTTGGA 180 AGACTTTTTG TCCATGAGTG TGAATGGATC CGCACTTAAC TCAGAATAAA TGCCGAGATG 240 TAAAGGACAC CCGCAGCCAT GGAGCACAGC GGCGGCGCAA CAGCTGTGTT GTTCCTGAAC 300 GCTTTTTCTC TGGTCTTAAA TTTAGACACC GAATCCTGCA GTGTCAGGAA AAGCTGGAGA 360 ATGCAGCTGC GGGCCGGGGA CTCGGCCGGA AAGCCCCGGC CGCCTCCTGC TTCCAGTGCC 420 CCGCAAGGCT CGGGCGGGAG ATGACTGTCC CCGTCCATGT TCTTTCCTGT GGAGTAGACG 480 CTGTGCAGCC ATCGGGTGAG AAGATATCGG CTTGGTCCTG GGCCCTGCCT TGCGGGCGTC 540 CGTGGGATAG CAGGTCTTGG GGCGCTGGGC CTTGTCCGGG AAGAGGCACT GGATGGGGCG 600 ATGCTCTGTA GGTCCTGCAG GCGCCCTGGC AGGGATGGGG TCCGAGGGCT CCTGTGTGCC 660 AGGCTCCTGA GATCTCCTGG CAAGCGTTCG AGGCCTGGCA GGTGCGGGGG CACACAAGGC 720 TGAGGTTCTG CCGGGGTGAC CCTCTGCAGG CCAGCGTCTT GTGGGAATAA AGCCCGAGCT 780 GGAGAACGCG GCCTGTGGGC AGGGGGTGGG GTTGGGGTGC TCCTACTTCC GTTTCCCCGG 840 CCTACAGGCG CTGCCCTTTG ACCCTGGAAG GGCTTTGGAG AGAGGGCCCT GCTGGGGCCA 900 GGGCCGCGTT GCTAAGGAGA CGAGGGCGTT TCATGTGAAC ACCACGTTAA CAAGCTGCTT 960 ATTTAAAGAT GGCATCTAAC GGAGATCTTT TGTTTCCCTC ATCACTTTAC CGAAGGACCA 1020 TACCAGACTC TGCGCTCGTC TCCTTTCATG TTTTGCTTCC GTTCTGCCTC TCCTCGCGTG 1080 TCTCTGCCAG CGCACATGCA CACACCTGCT GCTGTTCTCC TTAGCAGATC CCACCCTAAC 1140 ATTCTGTGGT AGGAAAACAA TGTTCTTCTC TTACTTGGCT AGATAATGTC ATGGTTAGAA 1200 ACACAGATTC TGGAGCCAGA TTCCCGGGGT TCGAGTCCTA TCTCGACCAC GTCCCATCTC 1260 CTGGTCAGGG TTAGGGCGCT ACCCCCAGCA TCTCCATGTT CCCATCTGTG ACACGTGGGT 1320 GGCAGCGCCT TCCTCCTGGC GGGGATCCCG GGAGCGGATG CGCTCAGGCC TCGGGATCTC 1380 GCGGGCCGTG TGCCCAGTGC TGCTGGCATG AGCTCGGCCT GGTGTTCGAG GCAGCCTGGC 1440 CAGTCCTCGG ACCTGTGCAG CCTGCAGAAG AAGGGGCCGC ACCTTGTGGA TAAGGAGTGT 1500 GTCATTCATC TTTGTGTTCC AGCCACTTTT CGTGGTTCCT 1540
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