| Tag | Content |
|---|
EnhancerAtlas ID | HS050-50350 | Organism | Homo sapiens | Tissue/cell | Fetal_stomach | Coordinate | chr4:4792760-4794000 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Six3 | MA0631.1 | chr4:4793574-4793591 | ATAAATGATACCCATTA | - | 6.25 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | TGTATTCATT CTTTCCTCAA ATGCATTTAA TGCATGGAAA GACTTAAGAC TAGTGCCAGG 60
CATGGAAAAT ACTCCCTAAG CGTTAGCCAC TATTCTTATG ATTATCATGG CATTGTTGTG 120
ATTGTCATCA TTCATTCATT CAACAAACAT CTATTGCACC CCCATGTGTG CCAGGCACAG 180
CCTTGGCACT GTGGAGTCGG CAATAAAAAA GGCAGAGTCT CTGCCCTGCT GGGAGCCCAG 240
CCCCTAAATG ATTCATCCCA CACTTAATGA GCTTGAGTTG TGATTCATGC CGGGGGTCCT 300
GAAAGCATGA AGCAGGGCCA CTGAGCTTAC CCGGGGCTTC CCTGGGGAGC AGCTGTCATG 360
AGTTGAGTCC TCAGGAACCA GCTGGAGTCA GCCCAGCTAA GAGTGGAGAA GAGCTCACGG 420
GGCTCCAGAG GCTCATCCAG GGCTGCTCAG CAAACCAGGC ATGAAGGCCA AGGCCCCTCC 480
GTGCTGGCTG CATTAACCAG CTTGTCGGGC CTCAGCTCCC AGGCCCAGAG TTTGGGACCG 540
GGCCAGGCAG GCTCAGAGCA GGCCAGGCAT TGGCAGATGC CTGTGTGCTG AAGGCAGGGT 600
AGCGCTGCCT GGCTGCCTCC CTGACCTCCC AGGGCATCTC CTTTGTGTGG CAGCACTGTC 660
CCCCATGCCG AGCCCCTTGG GATCCAGTTT CTGTGGAGGC CGACTTGCAA AACCCGGGGT 720
ATTGTCTTGT AACAGCAGGC TCTGGGGTGG GTTCAATGAA AATCCAGCCC TGCATGTCTC 780
TGTATTCTAA CCTGAAAAGA ATTATGTTAC ATCAATAAAT GATACCCATT ATGTGCCAGC 840
ATCCAGGGCT CTTAATTGAC TCGGGCTTAG TTAATGATTG GGAGAACATC CACGGAGAGC 900
CTGAGGCTCC AAAGGGAGGG GCTGGGGATA GATTAATAAC ATAAAGGACT GGATGGAGAC 960
ACTCCGTTCA ACTGCTGCTG GGCCCTGTGT GGAGCTGGCT TTGGCGTGTG ACAGTACAAA 1020
GTGGGATGGG AAGATATTTG ATGACAAAAT CCCTCATCTT ATGCTGAGAG GACCTGCTCC 1080
TTCCCTGCTG CTCAAATCAG AAGTTACAGC TTGAGACACA TCTGCTGCCT GCCTTCTCAC 1140
CACATTTAGT GAAGACACCC ACTCTAAGAA TCCTTGGACA AAGTGACCCC AAGGACTGGA 1200
CCCGTCTTAT CCTCGATAGT TTGGAGACTC ATTAGTTTTT 1240
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