| Tag | Content |
|---|
EnhancerAtlas ID | HS043-05065 |
Organism | Homo sapiens |
Tissue/cell | Fetal_heart |
Coordinate | chr10:28768250-28768960 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| MAX | MA0058.3 | chr10:28768740-28768750 | ACCACGTGCT | + | 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 |
| GH10I028478 | chr10 | 28767723 | 28768969 |
|
Enhancer Sequence | GCCTCCCAAA GTGCTGGGAT TACAGGTGTG AGCCGCCATG CCTGGCCTAT TTTTCCATTC 60
ATCTTATTTC TGATTTTGAT GAAACCCTTG ACTAGGGTCC CCAGTCCCTA AGGGACAGAC 120
CCTGTCCCAT AGCTGGGCAG TGGGTCTGGA GGGTTGGGTT TGTCTCCCCA CTCTGGCGGA 180
TCAGATATGA AGCTGGATCC CAGCCCAGCA GCGTGTGAAC GCCTTGTCTG TTGTGGCCAC 240
AAGTAATTTT CTCCAGCCAG CTTGCTATGT CACAGCTGCC TGGCCCTCAG GGACAATTGC 300
TGCTAGAAGC CTATTTCTGT ACTCTCTCCC ACCACTGTGG CCTTGGATTG ATGTTTAGCT 360
GTACAGCAGG GGAAAAGGGC CCCCAAGCAG AACATTCCAG ATCTTTTCTC TTGCCAGCTC 420
AGGCCCCTAT TTCCTGTTCC TCCGAAGTGA GAAGTACTAG TGGGATTTTT TAGAAATGCA 480
GCCTTCTCTC ACCACGTGCT GCAGCTCACT CCAAAAAGGG AGTTGTGGGT TGGTTCCCAG 540
AATTTTATTT CAATTCAGAC CTAATTGTTT TTTATTTGGA TGCATTGGGT GTCTTGTATT 600
TGGATTTAGA TGTCTTGAAG TCTGTGGTAT GAGGTTGGAA AAATTTCCTA GATTCAGTGT 660
TGGAGGATGT TTCTTTTGGT ATATCTTGTT TTCTTCATTC CAGTCAGTGT 710
|
