| Tag | Content |
|---|
EnhancerAtlas ID | HS050-06978 |
Organism | Homo sapiens |
Tissue/cell | Fetal_stomach |
Coordinate | chr10:6389260-6390630 |
SNPs | | Number: 2 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EWSR1-FLI1 | MA0149.1 | chr10:6390220-6390238 | GGAAGAAAGAAAGGAAAA | + | 6.41 | | NFIA | MA0670.1 | chr10:6390106-6390116 | GGTGCCAAGT | + | 6.02 |
|
| | 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 |
| GH10I006347 | chr10 | 6389067 | 6390962 |
|
Enhancer Sequence | GTGATCCTCC CCCGTCAGCC TCCCAAGGCA TAAGTTACTG GTGTGAGCCG CTGCGCTGGC 60
CTATATTATA TGTTTTTGCT GCTTCTGTTG GGGAAGAATT TGGTGTTTTA TCTGAGAGAG 120
ATGACAGGAA CCTTGGCCAG ATGCCACCCC CAGAAACTCA GTGTCCTTCT GTTGGTAGCT 180
GCTTGCCTCT TTGCTGCCCC TATCAGAGCA GAGTTGTTCA TTTGCTTCTC TGAGCACATC 240
TTGTGTGGAG TCTCGGGCCC CAGACAGCAG GGCTGCAAAT GACACACTCA GCTGCAAGGC 300
AGCAGTGATC TGTGGACGAG ATTCAAATCC AGAGAAAAAA ACGGAAGCCT CGAACTGCAT 360
CTGAAAACCA GCGAGAAAGA AGCAAATTCC TGTGAAATGG CACAGGCATC ATTTCAGCGT 420
TGACTCATTC TGCTCAAACC TGTCACCGCT CACACGGGAG TGGTCGTTGG AATAAGGGAC 480
TTCTCCTCAG GTGAATGACA AAGAAACACA GATTTGGATT TGCCCAGGTG TCTGGAGAGG 540
AGGCTGCCCC TGGATGCCGT GCCCCACTGT GCAGAAAGGG GATGCCCGGG GCATTGTCAC 600
CGCAGCGAGT CTGCACCTAC CATCCTCTGG CCCCTTTCTG CCACCTCTGC AGCATCTCCA 660
ATTAAATTTT AAAAAAGTAA AAGTGGGGAC AAGAATCATC TGCCTGCCTG TGTTTGGCCC 720
TCCTTCCAAG TTTTTGTGTT CTGTTTGAAA TCAAACTTAT GCTTTCTTCC AAAATGAATG 780
ACAGAGAAAA AAGAAAAAGC CACCCAGGCT TGAAAAGTGG TAGCTTCTTG CCGCCGACTT 840
CCTGCCGGTG CCAAGTCAGA GGGAGCTCTG CGTGTCCTCA GTTCACCCTC GCCAGGCCAC 900
ACCGCATGCA AATAAGAAGC TGTTTCAGTG TGTGCCCATC TGAGACGCTG ACATAAAAAA 960
GGAAGAAAGA AAGGAAAAAA ACCACCGTCA CCACCAACAA AAAAACCCAA AACTGATTAA 1020
TTCTCGTAGA TTGCAGCAGA GCAGGGGGCC TGGTGGTGAC ACATCCTGTT TTGCTGTTCA 1080
AGTTGTCATC CCCCAAGCCA ATAAGCTCCC TCATGAACGG CACCAGTTAT GAAGGGTGAC 1140
AAAGAATTCA AAACACTCAC AGGACAATTT TCCTAACCCT TGGTCTCTCG GAATGCTATT 1200
TTTTAGGCTA ATTTGTTTTG ATGAGAAAAC TATGCCTGCT AGGCCTATTT TTAAGCCAGA 1260
TTTGAAGTCA ACGCAGTTGG TATTTGATCT TGCAAGAACG ACAGAGGTGT CAGCAGCAGC 1320
TCTGCCATTT AAGAGCTGTA GCCTGGTGGG ACACCGTCCT GCAACCAGGG 1370
|
