| Tag | Content |
|---|
EnhancerAtlas ID | HS176-04706 |
Organism | Homo sapiens |
Tissue/cell | SK-N-SH |
Coordinate | chr10:28768130-28769130 |
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 | GAATTACAGG CGTGTTCCAC CACACCCAGT TAATTTTTGT ATTTTTTGGT AGAGATGAGG 60
TTTCATCATG TTGGCCAGGC TGGTCTCAAA CTCCTGACAT CTAGTGATCC GCCCACCTCG 120
GCCTCCCAAA GTGCTGGGAT TACAGGTGTG AGCCGCCATG CCTGGCCTAT TTTTCCATTC 180
ATCTTATTTC TGATTTTGAT GAAACCCTTG ACTAGGGTCC CCAGTCCCTA AGGGACAGAC 240
CCTGTCCCAT AGCTGGGCAG TGGGTCTGGA GGGTTGGGTT TGTCTCCCCA CTCTGGCGGA 300
TCAGATATGA AGCTGGATCC CAGCCCAGCA GCGTGTGAAC GCCTTGTCTG TTGTGGCCAC 360
AAGTAATTTT CTCCAGCCAG CTTGCTATGT CACAGCTGCC TGGCCCTCAG GGACAATTGC 420
TGCTAGAAGC CTATTTCTGT ACTCTCTCCC ACCACTGTGG CCTTGGATTG ATGTTTAGCT 480
GTACAGCAGG GGAAAAGGGC CCCCAAGCAG AACATTCCAG ATCTTTTCTC TTGCCAGCTC 540
AGGCCCCTAT TTCCTGTTCC TCCGAAGTGA GAAGTACTAG TGGGATTTTT TAGAAATGCA 600
GCCTTCTCTC ACCACGTGCT GCAGCTCACT CCAAAAAGGG AGTTGTGGGT TGGTTCCCAG 660
AATTTTATTT CAATTCAGAC CTAATTGTTT TTTATTTGGA TGCATTGGGT GTCTTGTATT 720
TGGATTTAGA TGTCTTGAAG TCTGTGGTAT GAGGTTGGAA AAATTTCCTA GATTCAGTGT 780
TGGAGGATGT TTCTTTTGGT ATATCTTGTT TTCTTCATTC CAGTCAGTGT TAGAAGGAAA 840
TTTTGTAAAT CTGTTAATTT TACTGCCTTT ACTGGATGTT CCAATACCAC TTGTTGTTTT 900
TTTGTTTTGT TTATTTATTT ATTTATTTAT TTATTTATTT ATTTTTTTGA GACATGTTCT 960
TGCTCTGTCA CACAGGCTGG AGTGCAGTGG CATGATCATA 1000
|
