| Tag | Content |
|---|
EnhancerAtlas ID | HS050-40865 | Organism | Homo sapiens | Tissue/cell | Fetal_stomach | Coordinate | chr2:242446230-242447420 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Zfx | MA0146.2 | chr2:242447038-242447052 | CAGGCCGAGGCCGC | - | 6.99 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | AGCACCTTAG TCATGTAAGT TACCAGATAC AGAATGCCAA AAGCAAACCA AAAATCTGTT 60
AGCTTAATTC AGCAACAGTC AGCAAGCCCC AGTCTCATCT GTGACCACGC AGGTCCAGGT 120
TGCCTGGCCC AACAGCTGCA CATGGTGTTC CGGGTCTCTA GGCTGGTCCG GTTTCCTCCA 180
AAGCAGCCCT GACTCCAGTT CCTGCCCCTA CGCGAACAGA CGCCCTTCCT GTTCCACTGC 240
AGGCCCAACT CTCCATTCAG CACATAGGAG TGAACAAGGA GGGCCACACA TTTTAGCGGC 300
GATTCCAACG CCTTAGGTAG AGCCAAGGCA TCAAGGAGAA TAAAACCGAA CAGCTAAGAT 360
GTAAGAAAAC CCAGCGGCCA GAGTCAAAAA AGTGGGGAGG GGTAGAGAAT GCAAGTCCCC 420
AGGCCCCAGG TTGGCTGACC CCACCCTCCT TCCCCGGCAA GCCCTTTGGC ACCAGCAGCT 480
GGTCCTCATT CCAGGCTAAG GGCTCGCCGT AGTGGCTCCC TCCGAGGCTG TCCCACCAGA 540
CGCTTAAAGG TGGCTCCATA GTGGAAACGA CTTCTTTAAA GAAGAAAGAT GAGTCTCATG 600
TTCGGGCAAC CGCCCGTCGC AGGGGTTAAA CGGTCCTGAC AGAGCAGCCT TTTCACCCTC 660
CCCTGGGCCA AAGCACACAC GTGTTCTCTG CTTTCCCTGC ACACCGGCCA CTCAGATCTG 720
CTTCTCCACA ATCTCAGCCC CTCAGCGCCC GCCAGGGTCT CCCCTACAGC CCCTGCCCAG 780
CCCAACACGG CCAGAATGAC CCGCGGCCCA GGCCGAGGCC GCAGGGTGGC CCCCGACCTT 840
CCACTGCCTT CGGATGCTGA CATGAGGTTC CCGCCCCGCG CTGGGGGCAG CGCCCCGTCC 900
CTGCGCCGGT GTCTCTTCAC GCACCTCCAC CGCCCTCGCA CAGGCGGAGC CACCAGGGGC 960
TCGGTTTCTA GAGGCCTGCG AGCTTCTGCC ACGCAAAACG CCACAGGCAC ACGGCAGAGC 1020
CCCGGGGCCG CCCTGCGCCC ACCTCAGGAC GGCTCCGCTG GTCGCACGAC GCGCGCTCCT 1080
TCCCTCACCC CACTGCCCGC TCCGGCGTGG CGCTCCCCTC TGAACCCCCA GGAGACTCTG 1140
GAGCCCCTCG GTGAGAGGCC GCTAGTCTTC CTGACCTGCA CCCTTCTCAC 1190
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