| Tag | Content |
|---|
EnhancerAtlas ID | HS050-45178 | Organism | Homo sapiens | Tissue/cell | Fetal_stomach | Coordinate | chr22:41444380-41446050 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| GLI2 | MA0734.2 | chr22:41445376-41445391 | AGCCCACCCACCATG | + | 6.51 |
| | | 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 |
| GH22I041047 | chr22 | 41443577 | 41446071 |
| Enhancer Sequence | CCGAGACAGG CAGATCGCTT GAGCTCAGGA GTTCGAGACC ATCCTGGCCA ACATGGTGAA 60
ACCGCGTGTC TACTAAAAGT AAAAAATTAG CCGGATGTGG TGGCGCACTC CTATAATCCC 120
AGCTACTCGG GAGGCTGAGG CAAGATAATT GCTTGAACCT GGGAGGCGGA GGCTGCATGG 180
AGCCGAGATT GCGCCACTGC ACTCCAGCCT GGGCAACAGA GTGAGACTCT GTCTCAAAAA 240
AAAAAAAAAG ATGTAAACAG GTGCTGACAG TTGTAACTAG TTGACATGCA CTTTTGTTTT 300
CACACCCACA CACTCCCATC AGTTTTTTTA CCTTTATGTA CCTAAGACAA CATAATCATT 360
AATGCTATTC TCCTTTCTGG TGCCTATTAC GATATTAAAG GGAAAATGCC ATTATAGACA 420
TTTCTAGGCG AATCGCACTG GAGCAGTAAA CACGTGGATG AACAGCCCGG AATCCACTCT 480
CATCAGATAA GAGAAGAATC CAGCTGCCTC TTGCTGCACC ACAGCTCCCT TTCCCTGGGG 540
CTGTGTTTCC GATTCCTCTT GGCTCTACTT TCCCGGCCTC TGCCTGGTGG CCTGAGAGCT 600
GCGGGCTATG GCTGGCCAGG GGGCGGGCCC AGGCGCGGAG CATGTGTTTT GAGCATTAGT 660
GGAATCTGTC GGATTAGTGC TTCCTGCTCA TGCTGGTTTC ACAGAGAGAG CAGAGGCAAG 720
ATGGATGCGG GAGGCACAGG CGTGTCCCCG CGGTCCTGTA GTGTGGGTAC AATGGCTTTA 780
TTTCAGACTT TGTCTGCCGG TTTCCAACTT GGCTTATCCA TGTGTCCGTC CCCTGCAAGT 840
CCACGCTGCT TCCGCTGTGG AGTCTACAGA CATCTGGTTA TCGAGGGAAG CATTTGTCCA 900
GCGAGGATTC AAAGCCAGAC ACAAAGCCAC CACTGGCTTG AGTACCATGG ATGGGGTTTA 960
TAGGGGAGTG AGTTCTGAGT CCCTGCCTGC TCCCGCAGCC CACCCACCAT GGCGAGGAGC 1020
AGCCGCTGAC TATGCCGACC TGTTTAGTGT CGCCAGTGAT TTATGGCCCA GTGGGGCCCA 1080
GCTGTTGGCC GTGGACACAG CAGCTGCTCA AGGTTAAGCA GGCCCTGTGT GAGGGATGCA 1140
AGTCACAGGA TGGACCCAGT GCAGTTGTTC CCTCTTGGGG TCAAGGGGGC GATCATGTTG 1200
CCAGTCTGAA AACCAACGCA AGCTAAGGAG GGCTGTTCCC TGCAACACAC ATGCACTTGC 1260
CCCCTCCAGC TAAGGCCCAA AGCTCTGCTC TAAGTCTGAA TCCGCTGCGT GGCTGTTGGT 1320
GCCAGGCTGA GCTGAGAGGC TGTTCAGGAG GCCTTGTGCA GCCCTGCAGG AACATGTGGG 1380
TTGTCAGAGC TGCTGCCCTG TTGTCCCATG GCATTACCTG ATTGTCACCC AAGAAGGAAC 1440
GTGCCTTGGA GTAAGGGCTG AGAGAGGAAG GGAACAGCCA GCTCTTTATG GAACCCTCAC 1500
CATGGGCCAG GCCCTGTCCA AATGCTTTCC TTGGGTTTTC ACATCTAACC CTTGCAACAA 1560
GTCAGTGGGG TAGACTTTAC TAATATTTCC CTAAACCTCC TGAAAATGGG AGTTCAGAGA 1620
GGGTGAGGAA ACTGACCAAG GTCACACAGC TAGGCTAGTG CCTGTCTCTG 1670
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