Tag | Content |
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EnhancerAtlas ID | HS050-40213 | Organism | Homo sapiens | Tissue/cell | Fetal_stomach | Coordinate | chr2:225349510-225351090 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
TCF7L2 | MA0523.1 | chr2:225350836-225350850 | AAAGATCAAAGGTA | + | 6.46 |
| | 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 |
GH02I224483 | chr2 | 225348493 | 225351270 |
| Enhancer Sequence | AAAAACAATT AAATTCAGTT TTTAGAAACG ACAAATTTGA GATCTGGCAA GATGGCCGAA 60 TAGGAACAGC TCCGATCTGC AGCTCCCAGC GAGACTAATG CAGAAGGTGG GTGATTTCTG 120 CATTTCCAAC TGAGGTACCT GGTTCATCTC AATGGGACTG GTTAGACAGT GGGTGCAGCC 180 CACAGAGGGT GAGCAGAAGC AGGGTGGGGC GTCACCTCAC CTGGGAAGCA CAAGGGGTCA 240 GGGAACTCCC TCCCCTAGCC AAGGGAAGCC CTGAGGGACT GTGCTATCTG GCCCAAATAC 300 TACGCTTTGC CCACAGTTTT TGCAACCCGC AGACCAGGAG ATTCCCTTGT GTGCCTACAC 360 CACCAGGACC CTGGGTTTCT AGCACAAAAC TGGTCGGCTG TTTGGGCAGA TACCAACTTA 420 GCTGTAGGAG TTTTTTTTCA TATCCCAGTG GCAGCCGGAA CCCCAGCGAG AGAGAACCGT 480 CCACTCCCCT GGAAAGGGGG CTGAAGCCAG GGAGCCAAGT GGTCTTACTC AGTGGGTCCC 540 ACCCCGACAG ATCCCAGCAA GCAAGCTAAG ATCCACTGGG TTGAAATTCT CACTGCCAGC 600 ACAGCAGTCT GAAGTCAACC TGGGACACTC AAGCTTGGTG GGGGGAGGGG CGTCCACCAT 660 TCCTGAGGCT TGAGTAGGCG GTTTTCCCCT CACAGTGTAA ACAAGGCCTC CAGGAAGTTC 720 GAACTGGGCG GGTGGCAAAG CTGCTGTGGC CAAACTGCCT CTCTAGATTC CTCTTGACTG 780 GGCAGGGCAT CTCGGAAAGA AAGGCAGCAG CCTGAGTCAC GGGCTTGTAA ATAAAACTCC 840 CATCTCCCTG GGACAGAGCA CCTGGGAAGA AGGCAGCTAT GGGCCCAGCT TCAGCAGAAT 900 TAAATGTTCT TGCCTGCTGG CTCTGAAGAG AGCAGTGGAT CCCACAGCGC AGCACTCCAG 960 CTCTGCGAAG GGACAGACTG CCTCCTCAAG TGGGTCCGTG TCCCCCATGC CTCCCTGACA 1020 GGAGACACCT CCCAGCAGGG GTCAACAGAC ACCTCATACA GGAGAGCTCC GGCTGGCATC 1080 TGGCAGGTGC CCCTCTGGGA CAAAGCTTCC AGAGGAAGGA GCAGGCAGCA ATCTTTGCTG 1140 TTCTGCAGCC TCCACTGGTG ATACGTAGGT GAACAGGGTC TGGAGTGGAC CTCCAGCAAA 1200 CTGCAGCAGA CCTGCAGAAG AGAGGCCTGA TTGTTAGAAG GAAAACTAAC AAACAGAAAG 1260 CAATAACATT CAACATCAAC GAAAAGAATG CCCATGCAAA AACCCCATCC AGAGGTCATC 1320 AGCATCAAAG ATCAAAGGTA GATAAATCCA TGAAGATGAG GAAAACCCAG TGCAAAAAAG 1380 ATGAAAATTC CAAAAACTAG AATGCCTCTT CTCCTCCAAA GGATCAGAAC TCCTCGCCAG 1440 CAAGGGCACA AAACTGGATG GAGAATGAGT TTGACAAACT GACAGAAGTA GGCTTCAGAA 1500 GGTGGGGAAC AACAAACTCC TCTGAGCTAA AGGAGCATGT TCTAACCCTA AGAAGCTAAG 1560 AAGCTAAGAA CCTGGATAAA 1580
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