| Tag | Content |
|---|
EnhancerAtlas ID | HS051-19572 |
Organism | Homo sapiens |
Tissue/cell | Fetal_thymus |
Coordinate | chr3:50471860-50473940 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chr3:50473673-50473692 | GCACCAGCAGGGGGCACTG | + | 6.85 | | ESRRB | MA0141.3 | chr3:50473740-50473751 | TCAAGGTCATT | + | 6.32 | | Esrra | MA0592.2 | chr3:50473739-50473750 | GTCAAGGTCAT | + | 6.32 | | Esrrg | MA0643.1 | chr3:50473740-50473750 | TCAAGGTCAT | + | 6.02 | | Gata4 | MA0482.1 | chr3:50473042-50473053 | GGGAGATAAGA | - | 6.62 | | Nr5a2 | MA0505.1 | chr3:50473531-50473546 | AAGGTCAAGGCCAGG | + | 7.06 | | TFAP2C | MA0524.2 | chr3:50472374-50472386 | TGCCCCAGGGCA | - | 6.44 | | TFAP2C | MA0524.2 | chr3:50472374-50472386 | TGCCCCAGGGCA | + | 7.22 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr3 | 50472646 | 50473258 | | chr3 | 50473332 | 50473392 |
|
| | Number: 2 | ID | Chromosome | Start | End |
| GH03I050435 | chr3 | 50472754 | 50473413 | | GH03I050436 | chr3 | 50473601 | 50473790 |
|
Enhancer Sequence | CTGGAAGGAA GCAGAAGCCA GGGGTGAGAC CAGGTGGTCC CACGTCCTCA TGCCATGGGC 60
CCTGCATACC CCTCTGCACA GCTCACCTCA GCACAGTATT CACCCGCACC CAGACCCTGT 120
CTTTGGCCTC TGAGAGAGGG CATGGAAGGC CAGCGCCCCC ACAGACTTGA AGGCAGGGCA 180
AGGCCAGGGG CTCCGTAGCT TGCATCTGGG ATGAGGGCCC AGTTTAGGCT GGTCATTGTG 240
GTTGGTGGGA TGGGGTTGTC ACTGCCTTCT CTGGGCCTCA GGGCCCCCCA TTTCAGGGTC 300
ATGAGCAGCC CTGCCCCCGA CTAGCTCAAG GTAACTGTGA ATAGCAGAGG GGAAGAGTGG 360
GCTGGAGAGG AGGCAGGAGG TTGAGGCGAG ATGGAGTCAA TAAGCACACA CCACATACCC 420
CATCCCAAAA AGAAGATGCT CACGCCCATG CATGGGCACA CACACAGCCA TGCCTCCACG 480
CTGCTCAGGC ATCTGGACCC TTTTTTGTGG GTGCTGCCCC AGGGCACTTG CAGGAACTAG 540
CAGGAGCTCT GGGCAATCCC ACGGGCTCCT CTGTCATTCA GGGCACAGAA TATGGGGAAT 600
GGGCACCAGG GAGGAAGGGG CAGGTTGGGG AGAATGAATC TGCCCAGCCT TCCTCCAAGG 660
GGGGTGGGTC TGTGGGCAGG TGCATGTGGC AGTGTAAATC TGAGGGTGTG TGTGTGTGTG 720
TGTGTGAGGG CTCAACATAT CCGTTTGTGT GCACGTGCCT GCGTGTTGGG GCTGGGGTGG 780
GGTGAGGGTC TCTAACCCCC CAGGGGCTTG TGAGTCTTAG GAGCAGATTT CTGCAAGTGT 840
CTTTGTTCAC AGCTGGGTCT TGGGTGTGTG CGTGTGCGTG TGCGTGTGTG TGTGCATTTG 900
TATGCATCAC ATACTGCTGC ATGTGTCTCC AAGCCTGACT GGGTCCATGT GTTCATTCAG 960
GTGACCCAAG GAGGTCTGTG CCCCAAGTAC AGGCTCCTTC ACCACCAGAG GTCACAGAAT 1020
AGGCTGCCAC GACTGAGCCG TGCCACCAGG CTGAGCAGAA GTGGAGGGAT GTGGAGAGAC 1080
AGAGAGGAGG TGATGAGGGG AGATAAGGAG GGGGGAGAGG CAGCCGATGA AAGACAGACA 1140
AGCAGAGAGA GATAAGGTCG GTAGAGTGAC AGCGAGAAGG CAGGGAGATA AGACCCTGTC 1200
ATCTGACAGG GGGATGGGGT GGGGGGGTTG GGTGCTGCTG GAGCCCCTGC TCTGCTGCTA 1260
CCCAGTGCCT GGCAGTCCAG GGGTTAAAGC ACCACACAAA GCCAGCTCAG GCAATCTTCT 1320
CCTCCTCCCG CCACCCCCAT CCCTCCCGGC TTCTCTTTTC TTTTTGTCCT TCTTTTAGAA 1380
CAAAATAATT TGTGGTGAAG TCGCTCCTTC CCGCAGAGTA GTGGCAATAA GGGGGCGAGA 1440
CTTGAGGCCT GGCCACATGG CCAGGGAGAA GAGAGGCCCC GAGTGAGTGC CAGGCCAGGA 1500
TGTTCCCTGG GCCCCTGGGC CCTGCCTCAG GACAGACGTT CACAGAGGGA GACAGTGTTA 1560
GAGACACAGG GTGAGGAGGG GTCAGACCCT GAGGATCACT GAGGAAAGGC AGGGAACCTA 1620
GAGCCTAGCA CCTTACTATT GGGGAAACTG AGGCACAGAA ACAGGAGAGG GAAGGTCAAG 1680
GCCAGGCGAT TGAGTGGCAA AGCCAGATCC CCCATCAGCT TTCACCCATC CTTGACAGAT 1740
CATTCTGGGG TGTGTGGCCA TGGTCTCAGC CACATCCACC GATGCCTCTG GAGAGTGGTG 1800
CCCCGACCCA TTTGCACCAG CAGGGGGCAC TGCTGCCCGG CTTCTCCTGG CCTGGGATGA 1860
AGTTCATACC TCAGACTCTG TCAAGGTCAT TACCAGGTGC AGCCACAGTC TGGGCTGTCC 1920
ATGGCTGTGT ACAGCCCCAG GACCTGAGGC AGGACCATGT GGTTCTCCTG GGAAAGTCCA 1980
GGAGTCCCTC CTCTTGGGCT CCAGGGTGCC CCTTGCAGCC TGGCATGGTA ACTGTGCTGG 2040
GGATCAGGGG GCTGCAGAGT GAGTGGGTCT CTAGGTGGCA 2080
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