Tag | Content |
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EnhancerAtlas ID | HS052-27115 | Organism | Homo sapiens | Tissue/cell | Fibroblast_foreskin | Coordinate | chr3:133259180-133260700 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
REST | MA0138.2 | chr3:133260194-133260215 | AACAGCACCATGGAGAGGCCC | + | 6.59 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| | Number: 1 | ID | Chromosome | Start | End |
GH03I133540 | chr3 | 133259552 | 133260642 |
| Enhancer Sequence | ATATGCTGCT CTTCACTTTA AGAAAGTGTT TATTTCCCCT CTCCTTATAT CTGGACTGGC 60 CTGTGACTGC ATTGGCCATA GAACGCATCA TAAGATGTTC AAGGACATCT GAATCTCAGG 120 CCTCAGGAAG ACTGGTAGCT TCTGTTTCCT TCCTCTTACA GTGCCTGTCC TTGGGGTGTT 180 CTTTTTTTTT TTTTTTCCCT TCAACTCTTT TTTTTGAGAC AGAGTCTTGC TGTGACACCC 240 AGGCTGGAGT GCAATGGCAT GATCTTGGCT CACTGCAACC TCCGCCTCCT GGGTTCAAGG 300 GATTCTCCTG CCCCAGCCTT CCGAGTAGGT GGGATTACAG GCACGCGCCA CCACACCTGG 360 CTAATTTTTG TATTTTAAGT AGAAACGGAG TTTCACCATA TTGGCCAGGC TGGTCTCGAA 420 CTCCTGACCT CAAGTGATCT GCCCACCTCA GCCTCCCAAA TTGCTGGGAT TACAGGCACA 480 AGCCACTGCG CCCAGCCTTC CTTCAACTTT TAAGTTCAGG GGTACATGGG ATGTTCTCTC 540 TCATTACCAG CCTATTCCAT GTGGAAAGAC CACATGGAGG AGAACCAAGA CTCTCCTGCT 600 GACAGCCTCA GCTGAGCTCC AGGCCAATAG CCAGCACCAA CTGCCAGCCT GGCAAGTGAG 660 TCATTTTGGA TTCCAGCCAT GTTGAACCCT AGTTGACTAC AGCTTCAACC AATATCATGG 720 AGAGCAGAAG AACTGCCAAG CTGAGTCCTG TTAACCCACA GATATGAGGG ATACTAAAAT 780 GATTGTTGTT TTAAGCCTAG GTTTGGGGGC AATGTGGCAG CCAGCCTCCA AGATGGCCCC 840 AGTGGTCCCC ACCTCCTGGT ATTCACACCA CTTTATAAGC CCTTTGCACT TTGTACCAGA 900 GCTGGCCTGT GTGACTAATA GAATACAGCA CGGTGTGTTA CTTCCTGGAT TAGGCTATAA 960 AAGACCTTGT GGCTTCTGTC TTGGTCACTC TTTCAGATCC CTCTTCCTGT TGGAAACAGC 1020 ACCATGGAGA GGCCCACATA GTGTGACCAA CTCCTCCCAG GACTTCCCAG GACTTTCCCG 1080 GTTCAGCACT GAAAGTCTCA CATCCTGAGA ACTCCCTCAA TCCTGGACAA ACCAGGATGG 1140 TTGGTCACCA TATGCCCATA TGGTAAGGAA ATGAGACATT TGGACAACAG CCAGCAAGAA 1200 ACTGAGGCCT CCTACACACA GTCATGTGAG GACACCATCT TGGGAGTAAA CCCTCCAGCC 1260 CCAGCCAAGC CCTGAGCTGC CTGCAGTCCC AGCTGAAGCT CAACTGCAAC CTCAGGAGAG 1320 CTTCTGAGCT AGAACTATTT GCCTAAGCTG ATTATGGAAT CCTGTCCCTG TGATGTATTA 1380 TTTTAAGCTG CTAAATTTGG GATAATTTAC TAAACAACAA TAATAGATTT TTTTTTTTCT 1440 CGAGATGGCG CCCTGCTCTC TCGTCCATGC TGGAGTGCAG TGGCACAATC TCAGCTCACT 1500 GAAACTTCCA CCTCCCAGGT 1520
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