| Tag | Content |
|---|
EnhancerAtlas ID | HS050-12922 | Organism | Homo sapiens | Tissue/cell | Fetal_stomach | Coordinate | chr11:72016910-72017900 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| HNF1A | MA0046.2 | chr11:72016931-72016946 | AATTAAATATTAACC | + | 6.11 |
| | | 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 |
| GH11I072306 | chr11 | 72017296 | 72020486 |
| Enhancer Sequence | GATAAGGAGA TTATAATTTG TAATTAAATA TTAACCTTTC TGACAGTATT AAAATTAAAC 60
CACTCAGAAT TCTTCATCCC TAATCAGGTG GTTCCTGCCC ATAACTACAT CTTCCCTAAT 120
AGTCCTGCTA GTTTATGGCC CTTTCCAGAG TGCTAATTGT TTCAATCGCT GCCAACCTGA 180
TGAATTGACT TAAAAATGCT ATCTCGGTCG GAGCGCATTA GCATGCTATG CGCTGCTTCT 240
TGCTTGCCTG CTTGTCAAGT GGGTCTGCTC CAGGTTTGGT GGAGGCAGAG CACAGCTACT 300
GGCAGAGCTA GGGGGAGTTT AAGAGCCTTC AGCCATTTAT GAAGCAGAAG GGGGCTCAGG 360
AGGACACAAT CTGAGCTACC TTGTTTCTGT GGCTGCCAGT GGGGCAGGCA AGCCAGAAAG 420
AGAACAGGAG TCCAAGACTC TGTGCTGCTG GGGCCACTTG GCTGGCAGAG GCCCAAGAAA 480
CTCCTCATTG CCTTGGCCAG GGAGGCTTTC CTTAGAAAGG CAAGAGCATC TGGGGTCTCG 540
GGCGACCTCC TGCCCTGGAT GCTGGGAAGG CTGGTAGGAG AATGTTTGGC TTTCAGTGAA 600
ATGTTTTTGC ACTCTCTCCG AGGACTGCTG TCTCTGCACA AAAGCATTTC CTTTCTCCCT 660
AAAAAGTTAA ACTGAGCAGG CCTTGGAAAG CCTGAGTGTG AACAAACAGG GGATGGGGAT 720
GGCCCTCTCC TGTGGAGAAT CCAGGGCTCT GAGCCATGGA GGAAGGGGGA CTATAAGTAT 780
CCCAGGCTCA AGACATAAGA AACCATGTTT AAAAGCTCAT GCAGGATAGT GAGAGGCAAC 840
AAGGCATCCT CTTATTCCCA CTTGTTTTCT CCTACAGCCC CCAAGACTCC CATTAGCACA 900
GCCATGACTG CACTGAACAG TAATGTTGTC TTTCTGAAGC TGTTTCCCCC TCCAACCTGA 960
GCTCCTTGGA GCAGGGGGAG TGTCTTAATA 990
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