| Tag | Content |
|---|
EnhancerAtlas ID | HS050-41836 | Organism | Homo sapiens | Tissue/cell | Fetal_stomach | Coordinate | chr20:34767220-34768350 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| PLAG1 | MA0163.1 | chr20:34768325-34768339 | CCCCTCTGGGCCCC | - | 6.36 |
| | | 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 |
| GH20I036179 | chr20 | 34767601 | 34767750 |
| Enhancer Sequence | CAAGCAGATG GGCTGGAAAC AGCCACCCTT CTGTCCAGGA ATGGTGTAGT CTTCAGTAAA 60
CAATGACCCT TTCCTCAGAG GCCCAGAGAG AGGCAGTTAT TACCTAAGGT CACAGAGCCA 120
AATGTTGGCT GAGCCAGGTC TTGAGGCCTG GTCTTCCAAC ACCATCCTGT GCTCTTTTCA 180
AGGCCTGGGG TGAAGGCAGA TGAGCAGGCC AACAACCTGT CCTTTCTGGC CCAGAGAGAG 240
AAAGCATGTC GGGAAGGGAT GGGGCAGCTC CCAAATGGCA GAAGGGGGTG GTAGGTGGCC 300
TCAGCAAGGC AGCCTGAGTA GTTGGAGACC TGGCGCCTCG AGGCAGAGAT GCCTCCACCC 360
AGGGCCCCTC CCCCTTGGCT GTGGTTGGTC TCTCCTGAAC TCCCTGGTCC CCTGGCTGGA 420
AAGCTGTAGC TGAGCCTGTT ACCATGACAG CGGGCAGCTG GGCCCAGGGA TGCCAGCTGA 480
CTCTGCAGGA GGGGGCTCGA GGAATTCTTC CTGAAGGTTC TGTCAGTTGG AGACAAAGAG 540
GCAGGCACAC AGACAGAGTG CACTCCTCGG GGGGCTGACA GATCCTCCGC CTGGGCTTCA 600
GGCTGTCCCC CAGGAGCCCC AGCCTGGCTG GGAGGCCTGT CTCTCATGAC TAAAGGGATC 660
GGAAAACATA TAGGCAGCCG AGTGTGTGGT GTTTGGTCAG GACCAGGAGC TTGGGAAAGA 720
CAGGTGGCTG GACCAAATGG TCAGGTCTCA GCATCCCTCC CAGAGGTGGC CTGCAGCCCC 780
TGCCAGCACA GCCCAGGCCT GGTGGATGTC ACTCCTTGTA GCCATCCCAA GTCATCGAGT 840
AAGTCTTGAT CGCTAGCAAG TACCTTATCC AGGAGAGCCA CAGTCTCTGC CTCTACCCCT 900
GTAACTTCCA GCCATTTATC CTCATCCTAC CTTCTGGTGC CCCAGTGGAG CAATTTTTTG 960
CCCTCTGTGA CAGCACCTCA GCCTTCTGAA GGTGGTCCCA TTGGTCCTTG TGGCCTGAGC 1020
TTCAGAGTTG GGTGTATCTC CTCCCAAACC TCAGTGCACC TGGGGCAAGG TAGGGCAAAG 1080
TAGGGCACCT GGGACAAGCT TTCCACCCCT CTGGGCCCCT GCTTCTCCTT 1130
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