| Tag | Content |
|---|
EnhancerAtlas ID | HS050-06137 | Organism | Homo sapiens | Tissue/cell | Fetal_stomach | Coordinate | chr1:227281740-227282760 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| HNF4G | MA0484.1 | chr1:227282478-227282493 | TGGACTTTGGACCCA | - | 7.05 |
| | | 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 |
| GH01I227092 | chr1 | 227280665 | 227282784 |
| Enhancer Sequence | TGTCATTGTC TTCAGGCCTA TGATGACAGT TAAGATCACA GCAGAGACTA GATATAAAAG 60
CAATGAAGGT GTTAAAGCAT TTTGGCAATT TATATTGGAA GGAGTATGGG CAGCATACAG 120
AAATGAATTC TAAGAGCTGA GAAAGAAAAT AAACTTTTTT TATCTGAGGA ATGTGAGACC 180
ATTTAAATTA TCAGGCCCAG AGAGGTATTT AAAATGTGAG AGCAGTCACA TCTCACTCCC 240
ACCTTGAGCT AAATAATCAC CTCTTGAGGC CACTTGCTAT GTGGGCTCTA AACTGATGCC 300
AAGTAGCCAT AAAATGCCAT ACACTGGAGA CCATGACTCA CACGCTATAG TTCAACAATG 360
AATAGCCAGT CACTAATCAA TGTTATTTTG TAAACCAGTG AAAATGCCTG TCAAACAACT 420
TTGTATCAGC CCAGCCCTTG CCTCCTTTTG CTTTTAAAAC CCTACTTGTA ACAAAGACCT 480
AATGGAGCAC TCCTCAAGGT AACCTGGAAG TGTGTTCCTG GCAGCTGTCC TCACTTTGGC 540
TCAAACAAAC TCTTTAAACA TATCCTGTGC CTCAGCTTCT TCCTTCAGGT CAGAAGGGTG 600
TTACCCCAAG GTGGGTAAAT AAAAAATTAA ATACAGCCAA ATTTATCAAA TGCACATACT 660
CATCTAGGAT TTGTGGTTTA ATGTGTTGAC TCAATATTCA GGTGTAGTTT TTCACTGCTA 720
GGCTGAGTAA TTGAAGCCTG GACTTTGGAC CCAATAGTGG CCTACAGTCA ATTAGCTCGA 780
GATATTTGAC TTACTGAGCA TAAAGGGTCT ACTGGCTCAA AGAGATGAGA ATGTCAGAGT 840
GGACCTATTA TGTGCAACCT GGTCAGCCAC CCACAAAGCA CTCCTTTCAC CAAGGCATTA 900
ATAAATACAC CAGTGAGAGG GCACATTAGC ATCCTGGAGA AACACTATGG TAGGTGTCTT 960
CAGATGACAG TCTGCAAATG ACAGCAGAAA ATGCCAGAAT GGAACTGCAT TGCCTGATTT 1020
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