| Tag | Content |
|---|
EnhancerAtlas ID | HS176-34202 |
Organism | Homo sapiens |
Tissue/cell | SK-N-SH |
Coordinate | chr6:31004900-31005940 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOXA1 | MA0148.4 | chr6:31005400-31005416 | GGCAAAGTAAACAAAG | + | 6.59 | | FOXP2 | MA0593.1 | chr6:31005404-31005415 | AAGTAAACAAA | + | 6.62 | | Foxa2 | MA0047.2 | chr6:31005401-31005413 | GCAAAGTAAACA | - | 6.27 |
|
| | 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 |
| GH06I031036 | chr6 | 31004710 | 31006155 |
|
Enhancer Sequence | ATAGGTCTGA TATAATTAAT CTGCCATTCT CTCTGGAGAA TGGTGCCACA TAACGGGGCC 60
AACACTGATC TCTGCTGTTA GCAGTTGAGG CACTCAGCCA TGGATTATCT GTCCAGCTTG 120
GCCTTGGTGA GGGGAAGGCC AGCTCACTGA GCCTTGCATA CGCTTCATCC CTGCCAGCCT 180
GTCTGCTTTG TCCATGTCCC TGCTGAGCGA GCACTAGAGC AGCTGGAAAA AGAGATTGGC 240
TGACGTCTGC AGAATGGATC GCTTGGTCAA CCTCATCATG GAAGATTTCC TCTGTAGTGA 300
ACGCCCATTG GTGAACAGTC ACATGGGATG CACATACTCT CACCATCTGT GCCCTTCCCA 360
AGAGACTCGT CCACCTTCCT CTTTCCCAGA CTTCCTTGTC ATCAATTCAC CATGTCTTTC 420
CTCACCCTGA GTTATCTAGC CAAACTGTTA GCCACTGCCT ATTGATCAGG GTTAACTGTA 480
ACTGGTCATC TCTTTGCCCA GGCAAAGTAA ACAAAGCAGA TGCATTCTTT ACAATTCGGA 540
TCACTGGGAG AATTTTCCTT CCCCACTGTC CTGCAGGGCT GCCGTGAGTG GGGTGGTAAT 600
GCTGCAGCAG CCTGCTCTCT GTGGTGTTAG AATAGCATGC AGAACCACCC ACACACCAGA 660
GGAAACCAAA TCTTTCCTTT CTCAGTCAAC TAGACATAGG AAACCCTTCA TGTGACTGTG 720
ATTATGGAGA GAGAGGTTAG GAATGTAGCT GGAGATGCCA CTGGAGTTAC AGCTGCCTAC 780
TCATGCCTCT TACTTGTGCC TTGAGGAACT AACTCAGCCA AATTCGCAGG CACCACTTCC 840
ATTCAAGGAG GTGAGCACTG CTAAGTATGC CCAGTCTAGT GTGGTGGTGC AGACAACACC 900
CAGTTCATAA AGGGCAGCTC ATGTTTCATG AACCCTCGCA TGCTGAGGAC CCAAGATTAA 960
GTCAGATGCT AGGATGTGGA AGAGGGCTTG CTTTTGCTCC AAAACTCTGG GGACCTGTGC 1020
CGTGGCTCTT CTACTAGCTA 1040
|
