| Tag | Content |
|---|
EnhancerAtlas ID | HS050-06020 | Organism | Homo sapiens | Tissue/cell | Fetal_stomach | Coordinate | chr1:224390700-224391810 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| RREB1 | MA0073.1 | chr1:224391013-224391033 | GGTGAGTGTGTGGGTTGGGG | - | 7.16 |
| | | 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 |
| GH01I224202 | chr1 | 224390586 | 224394441 |
| Enhancer Sequence | TACAGGTGCA TGCCACCACG CCTGTCTAGT TTTTGTATTT TTAGTAGAGA TGGGGTTTCA 60
TGACGTTGGC CTCGAACTCC TGATCTCAGG TGATCTGCCC ACCTCAACCT CCCAAAGTGC 120
TGGGATTACA GGCGTGAACC ACTATGCCCG GCCCAAAGTT TGTATTTCTT AAAAAGGATT 180
TTACAATGAT AATTTTCCTC AAATTCAGAG CCCGCTTTCT ACTTAGTATA ACTGATGGGG 240
TTTTCTAATG ATAATATGAA CCGTCCCACT CCCAGGAACA CAGGCAGCAG GCCAAGCAGT 300
GGCTCTCAGT GAGGGTGAGT GTGTGGGTTG GGGGAGGGGC AGCCCATGAA CACCCCAAGC 360
TACTTCCACA CTCCAATGGT CAGGAGAATG CAGAATTGAA AGCAGGAACA GGAGTCTGTG 420
GCCTGGAGCT CACATTTAAC CAAATAGTTT TCAGAGCTGG CTCAGAAACA GTTCTCCAAA 480
CCACAGCACT CTGCAAAGCC CAGCTGAGAT CATCAGATGG CCATCCCAGG ACAAGCAAGC 540
AGAACTCCTC GGCCTGGGGT CCTGTTTGCC AAAAGGAATC TGGATGTTGT GAGTGCCTCA 600
AGTCACTGAC TCCCCCTCCT CATGACCAGG GGATGATGAG CAGCTGTTTA ATAAGCCACC 660
GGTGTCAAAC CCGGTGGCCG GGGGCCCAGG AAGAACCCCG ACTTGGGAGT GCAGCCCCTT 720
AGGCATCTCA GAGCCAGGGA CAGGAAAGAA AGACAGGTTG TGTTGCCAGT GTGACTGAAG 780
CAAATTACCT TCCCTGGGCT GGTTTCCTTT ATCTATCTTG TCTATCTTTT CTTACCTCCC 840
TCCCGGGACC TTGAGATGCC TTGGAAATCA GATGGGAAAA GCACTGTCAC TCACTGCAGG 900
GGTTGTGGTA ATGCTGGTTA CTGATGCCAC TGGGAACACC AAGCTACAGG AGTCAGTCAT 960
TTGGGACAGT GCCAGCAGTC AGAGCACAGG TCACACTTGT TCCAAACCAT GGCAGTCGGT 1020
GCTTGCTGCC CAAACTATTG TCTGAGTTTA TTTTTTAAGA AATAAAAAAA AAAATTATCA 1080
TAGAATACAA AGAACATAAA ATACACCATT 1110
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