| Tag | Content |
|---|
EnhancerAtlas ID | HS050-02153 | Organism | Homo sapiens | Tissue/cell | Fetal_stomach | Coordinate | chr1:46931540-46933290 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| KLF5 | MA0599.1 | chr1:46932182-46932192 | GCCCCGCCCC | + | 6.02 |
| | | 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 |
| GH01I046466 | chr1 | 46931725 | 46933408 |
| Enhancer Sequence | GGGCTTTGGA GTCAGGCAGC CCTGAGTTTC AGTCTCTGCA TTACTATTTG CTAATAGTGT 60
GCCCTTGGCT GAGGGCTCCC CCCAAAATGC TTTACCCTCT GCCCCAATGC TTGTCCTCTA 120
GACATTCCCA GAGCAGGTTC CTTCATGCCA TGCAGATTTC AGCCAAAACG CACCTCCTTA 180
AGAAGCCATC TTTGACCACT CAGTCTCATT TACCTCCCCT TCCCCTACAG TCACTGCCAC 240
ATCACCTTGC TTTATTTTCC GTTCATTTAT TTCTTGTTTC CTGTGTGTCG CCTGCCTCCT 300
TCACTAGAGT CAAATTCCAC GGAGGCAGAG ACGGGGTCGG TGTGGCTCAC AGGGGTATCT 360
GCCGAACCCC AAACAGCGCT GGACACACAG AAGGCGCTGG GAGAAGGAAG AGGCCTCTCT 420
GAACCTGTTC CCTCACCTGG AAAGTGGGGC TAATCACATA ACCCTGCAGT CTCTGAGGTG 480
GTTGTGAGGG GGATTCAGAG AGGGGACCCG GGGAGCTCTG AGCGCAGTGC CAGGCCCGGA 540
CGTGGTCACC GCCTTGTCAC TTGCGCATTT CATGCTCTGG CCTCCCAGGC CGGGCGATGC 600
GGCCGCGGGG CTGCAGCTCC CGGCGAGGCC CGCCAGGCCC CCGCCCCGCC CCGCCCTCCT 660
CGGGCCCCGC TCCTTCCCAG GCGCCCCCGC GCCGCCGGCG CTTTGAAGTC CCAATCCGGC 720
AAATAGAGTC AATCAATTAT GAAGGGAACA ATCTGGCGGC CCCTCGGGGA GCGGCGGCCG 780
AGCGATCCCG GGGGATTAGG CCGCAAATCG CGCTGAGCCT CCCTAAGTGA CAGCGAGAGA 840
ATCGCGCGCG GCGGCGACGG CGGCGGCGGG AGCGGGAGGG AGCGCGGCCG CTAACCCGAT 900
TATGCAGATC CGCGGGGGGC GCGGATTAGG CCTCGGGGGC GGCTTCGCCC TAAGCGGCTC 960
TCGGATTTGG GAAAAGTTTA CTCGGGCGGA GGGGGCGGAG ACTCCCCCGG GCGGGCGGCC 1020
GGGACTTCTC CCAGCCGGGT GAATGGAGGA CCCGCCTGCA GGAGCAGCCG CGAAAGAGTG 1080
GAGCGGGCGC GCCTGCTGAG CCACAGCCAC AGCAACACTT TGCAGGCGTG CACACTCACA 1140
CGCACACCCA GGCCACAACA GCCGTGTCTG CACCAGCCCA CGGGCGCACG CGCGCTGCCC 1200
ACGATCACCC TCCCAAGCCA CAAAACACTC GCGAACGTGC GAGGCCGCAC CAGCCCACAT 1260
AGCCAGACCC ACGCCGGCTC ACACGCGCAC GCAGCACTGC CTCGTGCTCA CACAAGCATG 1320
CACGTACTCA CAGACACGCA ATTTGATGTT CGGATACCTG CCTCCTGTGG TTCCAGCAGA 1380
ATCCCTCAGT GACACAAGGT GTCCCTGCCA GCCTATGTAG ACGTAGGACT GGTGCACGGC 1440
CCTGCACCTG TGCTCTCCCA CGGACCTCCC TGCAGCTCCT CTCCTCTGAA GGACCTTGAG 1500
GACAAGTGTG TGTTAGTGTC TGTGAGTGTG TGTGTGTGTT TGAGCGTGGC CTGTCTCTGG 1560
AGTCTGGGCC CAGTTTTGGC TTCTGCAACT GGGGCCTTCT CAGGGTAGGT GGAAAAGACT 1620
GAGGCAGGAC GCTGGGATGG AAACAGGCCG AGTCCTCTTG GTGACTCTGG CTAAGGGGTC 1680
CTCTCCGCAG GGCTGGGGAT CCAAGACATT CCTCACCAGG CCCCTCTGGG CCAGCCCCTT 1740
CCCTGAGGTG 1750
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