| Tag | Content |
|---|
EnhancerAtlas ID | HS051-18034 | Organism | Homo sapiens | Tissue/cell | Fetal_thymus | Coordinate | chr21:44036190-44037410 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| TFAP2A | MA0003.3 | chr21:44036724-44036735 | AGCCTCAGGCA | + | 6.32 |
| | | 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 |
| GH21I042616 | chr21 | 44036511 | 44036910 |
| Enhancer Sequence | CACACACATC ACACCATACA CATACCACAC ACACATACAT ACTCATACAC ACCACACACC 60
CATATACACA GACACCATAC ACACACCACA CACACATATT CACACAGACA CATACACACC 120
ACATATACAT ACACACAAAC AGTTGCACAT ACATACACAC AGACACACAC AAGTACACAC 180
ACTACACAGA CAAGCACACA CATCACACAC ACACACAGAC ATGACCCCTA GCCATGCCCA 240
ACTTTGCACT GGTCACTAAT AATTTTTCTG GTTCTACCAA TATTTACCGC TCTGATCAGG 300
GAAGTGTCTG CATTTTTCTA TTTCAAAGCT GTTCTGTAGG TATCACGTCG GGGGTGGTAA 360
TATTGGCCAC CCTACGTCCT GTGTGCAGAG AAGGAATGAA GAGCGATTTG TGAACGCGAA 420
GCAGCAAAGC TACTAACGGG TGCAGTTAAG AAACAGAACA ATCAAGAAGA AACAAGAAAA 480
CGCCCTCCAG GAAACAGAAA CCGGGTGCAG AGGCACTGTC TGCAGACCTA CTGGAGCCTC 540
AGGCAACCTG CGGAGGAAAA GCCCCAAAGT TCTTTTCAAT CTTTGCTCCT GATAGAGAAA 600
GACGGTGTTG CACCGTTCTT TTCATTTGCA TGCGTGGAAT TTCCAGTGAG GTCCACGCTC 660
GCTGGCTCGC TGGCAGCTCC GTGGAATCCG CCCCACCCTT GCAGAGCTCT TTCATTGATT 720
TGAAAGAGCC TCTGTGTGCA CATAGTGCGA CTGTTCCGAA GTCTTTATCA CAGTTACTGG 780
TGATGCTTTT TTCCAGATGT CCTCGACGTG CACCCATGAA GGGCTCCACC TGAGAGTGCC 840
AGGGTCCTCC GTGGGATGGG GCTGGAGGGG GTGCTCTTGC CGTCCTGGGC TCCCAAGCAG 900
CCATAGGAAC AATAGGGTGA TGGGGTCCCA GAGATAGAGG CCAGTGACAG CAGCGCTTTG 960
AACCCCTCAC ACGGGCACGG GCCCTCTGGC AGGGATGGGC GTCCCGGTCA CACGGAGATG 1020
GGGGCTGCTG CTGCCTGCAG GTAGAGGAAG GGACGTGTTT GGCAGTCCTG TGACCCCTGG 1080
GCACCTCGCC TCCCCCACGG CCGGCTCTGC TTGTAAACAG ACAAGTGCAC AAGCGCAGCC 1140
CGGTGAAGGC ACAGCGGTCC CAGGAGGCAT CTGGGCTGCA CCCCAGCGAG CCGCCCATAC 1200
ACGTGGAGAT GCCGGCCAAG 1220
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