| Tag | Content |
|---|
EnhancerAtlas ID | HS050-53677 | Organism | Homo sapiens | Tissue/cell | Fetal_stomach | Coordinate | chr5:33726530-33727600 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ZNF263 | MA0528.1 | chr5:33727433-33727454 | CCTCCTTGTTTCTTCTCCTCC | - | 6.21 |
| | | 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 |
| GH05I033725 | chr5 | 33725460 | 33726784 |
| Enhancer Sequence | TTAGACAAAT TAAACTTAGA AGAGTTTAAC TGAGGGGGAG AAAAAAAGAT TTGCAAATGG 60
GTCAGCCCTC ACCCAGAACA GATTCAGAGA GACTCTGGAC CTGTCTCATG GTCAGAGGAC 120
ATTTATGGAC AGAAAAGGAA AGCAAGTACA GAAACTGCTG GATTGGTTAC AGCTGGCATT 180
TGCCTTATTG GAGCACGGTT TGAACAGTTG GCCATCTGTG ATTGGTTGAA GTGTGGCCAC 240
TGTAATAGGC CGAGATTCAG CTATTGTTAC TGAAGCTTAC TCCTAAGTTA ACTTTTGAGT 300
TAACATATTA GATTGCAGTT CAGACTTAAG AATTCAAATA TGCAAGTGCA GAGGCTTTCT 360
TGGGCCAAAT TCAGCTTGAT GTAACAGTAC TATCAGAATC ATCCTTACAT GTGTGTGGTG 420
CCCCGCAGTT TATAAAGTGC CCTCACTCTG AAGCCATGTG AATGCATCCT TTTGGACGGC 480
CAGATCCAGG AATCCGCCTG GGCAGATGAG GCATCTCCTG GGCTTGGATC TAAGCCAGCT 540
GCAGTTTGCC TCCTTCCAGC TCCAGAGGAA ACTCCTGGGT GAATCAAATC TCTAGTCGAG 600
TCAGCTCACC GCCTCCAGCA GGCTCTCACA AAGCTTCCTC TCTCTCTCCT CTCACCTCTC 660
CTGGAGGCGC AAGGCAGTTG CCACCTGCCC TATGCTGCTG GACACTGCAG AGACAGGATC 720
ACCAAGCGCA AAAGCAAGGC AGGGTTGGCC CAAGCACAAT GAACTGTGGC TGCCGCTGGA 780
CCTGTGTGTC TGGGTCGAGG TCAAGCCTCA CCACCGAGAT CTGGCCTGGG TGACGACGCG 840
TGTGTGTCCT CGCATTTCTG AGTGAATTCT CAGTTATTCA AGAGAGGGTC CATTGGGCTC 900
TCGCCTCCTT GTTTCTTCTC CTCCATGGAG GCATTTCATC GCTTTGCAGC TGCCTCTCCG 960
ATAGGAGGAA GTTAACATAG CTGTTTTCTG TGAGCAACTC TGCTTTGAAG TTAGAGCAAA 1020
CCCAAAGCAA ATGAAGCATT AGCTTTACAG ACTGTCCTGA GGTATCCCTT 1070
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