| Tag | Content |
|---|
EnhancerAtlas ID | HS098-48141 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr6:31004470-31006200 |
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 | ATGTGACATT AACCTGTTGT AATAAAGGTC AGAGTTGAGG ATGCCTTGGG GGAAAAGGCT 60
GACCGGGAGA AGGCATGAGA AAGCCTTCTT GCAGGGGCAG ACAGGGGAAG CTGAGAATGT 120
TCTGTGTATG ATCTGGGTGG TGATTACAAG GGTGTATAGA TATGTAAAAC TTCATTAAAA 180
TGTGCACATG AGATCTGTGC ACTTTATGGT ATGTAAGTTA TGTCTCAATT TGAAAAATGA 240
AAAAGATATT CTGAGGCTAT TTTCTCAGCA TATTATGATT TCCTTGGTCA GAGAATGTGG 300
TTGGAGACAC ATGACGATAA ATGAGGCATT TGGTAAGCCC AAAGACAGTG GTGCTGCAGG 360
AAGCATTGTG TGCAAGGGAG GCAAGCAGCT ATTTTCAATG AGGACAAATC ACCTCTCTCT 420
TTAGGTTGAA ATAGGTCTGA TATAATTAAT CTGCCATTCT CTCTGGAGAA TGGTGCCACA 480
TAACGGGGCC AACACTGATC TCTGCTGTTA GCAGTTGAGG CACTCAGCCA TGGATTATCT 540
GTCCAGCTTG GCCTTGGTGA GGGGAAGGCC AGCTCACTGA GCCTTGCATA CGCTTCATCC 600
CTGCCAGCCT GTCTGCTTTG TCCATGTCCC TGCTGAGCGA GCACTAGAGC AGCTGGAAAA 660
AGAGATTGGC TGACGTCTGC AGAATGGATC GCTTGGTCAA CCTCATCATG GAAGATTTCC 720
TCTGTAGTGA ACGCCCATTG GTGAACAGTC ACATGGGATG CACATACTCT CACCATCTGT 780
GCCCTTCCCA AGAGACTCGT CCACCTTCCT CTTTCCCAGA CTTCCTTGTC ATCAATTCAC 840
CATGTCTTTC CTCACCCTGA GTTATCTAGC CAAACTGTTA GCCACTGCCT ATTGATCAGG 900
GTTAACTGTA ACTGGTCATC TCTTTGCCCA GGCAAAGTAA ACAAAGCAGA TGCATTCTTT 960
ACAATTCGGA TCACTGGGAG AATTTTCCTT CCCCACTGTC CTGCAGGGCT GCCGTGAGTG 1020
GGGTGGTAAT GCTGCAGCAG CCTGCTCTCT GTGGTGTTAG AATAGCATGC AGAACCACCC 1080
ACACACCAGA GGAAACCAAA TCTTTCCTTT CTCAGTCAAC TAGACATAGG AAACCCTTCA 1140
TGTGACTGTG ATTATGGAGA GAGAGGTTAG GAATGTAGCT GGAGATGCCA CTGGAGTTAC 1200
AGCTGCCTAC TCATGCCTCT TACTTGTGCC TTGAGGAACT AACTCAGCCA AATTCGCAGG 1260
CACCACTTCC ATTCAAGGAG GTGAGCACTG CTAAGTATGC CCAGTCTAGT GTGGTGGTGC 1320
AGACAACACC CAGTTCATAA AGGGCAGCTC ATGTTTCATG AACCCTCGCA TGCTGAGGAC 1380
CCAAGATTAA GTCAGATGCT AGGATGTGGA AGAGGGCTTG CTTTTGCTCC AAAACTCTGG 1440
GGACCTGTGC CGTGGCTCTT CTACTAGCTA CCCAGTGTCT CCACACAGCT TTCTGATGTA 1500
CCACAGACAT TTTAGGCAAC ATTGGATCTA GTCAGCAATG TCTCAAGCAG CCTTATGGCC 1560
TTGCTTTGGT TCCCACTTGA AAGTGGGGAA ATATGCGCAG ACGGAGCCTA GAGATGAACT 1620
TTGAGTAAGA TGTTATTTAT GTTCTTTTTT TTTTGAGATG GAGTCTTGCT CTGTCGCCCA 1680
GGCTGGAATA GTGGCACGAT CTTGGCTCAC TGCAACCTCC GCCTCCCGCC 1730
|
