| Tag | Content |
|---|
EnhancerAtlas ID | HS050-59110 | Organism | Homo sapiens | Tissue/cell | Fetal_stomach | Coordinate | chr6:80373080-80374060 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| REL | MA0101.1 | chr6:80373812-80373822 | GGAAATCCCC | - | 6.02 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | CTTCTTTCTG TTTGTTGGTT TTCCTTCTGA CAGTCAGTTT CCTCAGCTGC AGGTCTGTTG 60
GAGTTTGCTG GAGGTCCACT CCAGACCTGT TTGCCTGGGT ATCACCAGCA GAGGCTGCAG 120
AACAGCAAAT ATTGCAGAAC AGCAAATGTT ACTCCCTGAT CCTTCCTCTG GAAGCGTCGT 180
CCCAGAGGGG CACCCGCCTG TATGAGGTGT CAGTCGGCCC CTACTGGGAG GTGTCTCCCA 240
GTTAGGCTAC ACAGGGATCA GGGACCCACT TGAGGAGGCA GTCTGTCCGT TCTCAGAGCT 300
CAAACATCGT GCTTAGAGAA CCACTGCTCT CTTCAGAGCT GTCAGACAGG GACGTTTAAG 360
TCTGCAGAAG TTTCTGCTGC CTTTTGTTCA GCTATGCCCT GCTCACAGAG GTGGAGTCTA 420
TAGAGGCTGT AGGCCCTGCT GAGCTGTGGT GGGCTCCACC CAGTTTGAGC TTCCTGGTGG 480
CTTTGTTTAC CTACTCAAGC CTCCCCAGTG GCGGCCGCCC CTCCCCCAGC CAGGCTGCTG 540
CCTCGCAGGT TGATGTCAGA CTGCTGGGCT AGCAGGGAGC AAGACTACCA GGGCGTGGGG 600
CCTGCCAAGC CAGGCATGGG AGAGAATCTC CTAGTCTGTC AGTTGCTAAG ACCTAGGAAG 660
AGCACAGTAT TTGAGTGGGA GTGTCCTGTT TTTCCAGGTA CAGTCTGTCA TGTCTTCCCT 720
TGGATAGGAA AGGGAAATCC CCCAACCCCT GTCCTTCCCA GGTGAGGTGA CGTCCCACCC 780
TGCTTCAGCT CGCCCTCCGT GGGCTGCACC CACTGTCCAA CCAGTCCGAA TGAGATGAAC 840
CAGGTACCTC AGTTGGAAAT GCAGAAATCA CCTGTCTTCT GCATCGATCA CGCTGGGATC 900
TGCAGACTGG AGCTGTTCCT ATTCACCCAC CTTGGAACGG ACTTGTGATT GGATTTAATG 960
TTTAGCTCTT TTTGCATGCC 980
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