| Tag | Content |
|---|
EnhancerAtlas ID | HS050-35134 | Organism | Homo sapiens | Tissue/cell | Fetal_stomach | Coordinate | chr2:9242830-9244310 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| KLF5 | MA0599.1 | chr2:9244213-9244223 | 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 |
| GH02I009102 | chr2 | 9242319 | 9244743 |
| Enhancer Sequence | AGCAACAACT GCAGTTCGGG GGATAGACAC AGAACGGTGG CCTCTCGTAT GTCCAAAGAA 60
CAGAGAAGTT TGGAGGTTTT ATGAAGAGGA GAAATGCTGT GTATTGTTTT GAAATAAAGT 120
TCCTTGGCAC TAGTAAGGTT TTGGGGATGC TGGCGAACAC TGATTTGTGG GTGATGGTGT 180
TAGATTTCAG CAGGTTGTTC CAGTGGCTGT TAGATAAAAC TGGTTTCAGG TTACACCTGG 240
CAGTTCCAGC AGCCAGGTCT GCAGAGAATC GTATGCTTGA AGGAACGTCT TGTGCCTCAA 300
GCGCTTTACC CGCAACCTCT GGACTCTGTT TTAGTTGAGT GTGACAAGAA AGACCCAAGG 360
CGTATGAAGC TTTGACCCTG TTTTGTAAAC TCCCTTTGAT GCGGTCAGAG TTCATTTGGG 420
GAAACTTCTG GGAATAGTCA ACACGGCCGG TTGGAAACGG AGGTGGAATT CAGTGGTTAC 480
AGCAGAAGCC TGCACTCTAT CGTCCAGTGA GAGCAGCCCA GGGATGGGCA CTCATGAAGG 540
AGAGTGATGC TGCCCACAGG AAGCAGGCCA GTGCTGAGCA GAGAGAACCA CAAGAAAAGC 600
AGACAGGTCT GCCCGCGTTT GAGCTGGTAT CACTTGCCCA GCAGGCAGGC ATGGGGTGAC 660
ACATGACTGG GCGAGCCACT CGCTGGGTGG GGCATTCACA CAGGTCAGCT CAAACCAGAT 720
GGAGCCTGGG ACTGTGACCA AGGAGCGAGT GAAGGTCAAA GCCACACATG GGGCTGAGGG 780
GCCAGGTGGC CGCCTTATGA GATCGAAGGC GGGAAGCTTT GGAACAGGGC AAAAAGGGGA 840
GCCCAGGGTG AGGGGAGAGG GCCGAGCAGC TCGGATCTCT GATGGTGAGC TGTGCAGAGA 900
TGGGGAAGCG CCTCTTTTCC TCTTTCATGT GGGTGTCAGG GGGGGTCCAG GCCTGAGGGA 960
GCCAAGCTGG AGGGTGCAGG GTTTCGCGTC TGCCTCGGAA CTGGATGTTT GAAAGCAAAG 1020
GTGAACGGCC CAGCAGGCCC GCTGGGGCAC TGGGAGAACT GGTTTTTGCC ATTTTAGGAA 1080
TTGTTTGGCT TTGGCTTTTT TTCTCACTAA GAAATTGGAA TCTGAAAGAG CCTTTCAGCT 1140
TATTGTTGAA AATCCATCAG GACCTGAAAA TTAGAGACCG GGCCTGAGCT TTCAGCACAT 1200
TTAAACTCAC GGGAGCGAGG TGGAAAAGCC ACAGGAAGTG GATGCACTAA TTTAGAAAAT 1260
AGGGAGAGGG AAGACAGCGC CTGTCCCCTC CCTGATTGAC CACAGGTAAC CCCTGGTCTC 1320
TCTGTCTACT GAGGCTGAGT GGCCTGTTCT GGGTCTGACT ACCCTACCCT GGGGCCTGAC 1380
TCTGCCCCGC CCCTCGCAAC ACTCAACAAA CGCTTGTGGA AGGAGTGAAC AAATGACAAG 1440
TCACGAAACC TAAATACAGG TATGTCACAA GAAGCCCTCC 1480
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