| Tag | Content |
|---|
EnhancerAtlas ID | HS073-07422 |
Organism | Homo sapiens |
Tissue/cell | GM19238 |
Coordinate | chr19:16944210-16945310 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Nr2f6(var.2) | MA0728.1 | chr19:16944226-16944241 | AAGGTCAGGAGTTCA | + | 6.04 |
|
| | 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 |
| GH19I016833 | chr19 | 16944341 | 16945767 |
|
Enhancer Sequence | GAGATGGGTA GATTACAAGG TCAGGAGTTC AAGACCAGCC TGGCCATCAT GGTGAAACCC 60
TGTCTCTACT AAAAGTACAA AAATCAGCCA GGCGCAGTGG AGCATGCCTG TAATCCCAGC 120
TACTTGGGAG GCTGAGGCAT GAGAATTGCT TGAACCTGGG AGGCGGAGGT TGCAGTGAGC 180
AGAGATTGTG CCACTGCACT GTAGCCTGGG TGACAGAGCA AGACTCCGTC TCAAAAAAAA 240
AAAAAATTCT GCTGCTTCTC TGTGCAAGAC CCTCTCTGCC ATCAGCCTGT TGTCTCCTGA 300
AAGCCAAGGA GCGAGTCTCA GGGTTTTTTT TTTGCCTTTT TTGAGAAGGA GTCTCGCTCT 360
GTCACCCAGG CTGGAGTTCA GTGGCGCAAT CTCGGCTCCC TGCAACCTCC ACCTCCTGGG 420
TTCAAGAGAT TCTCCTGCCT CAGCGTGCTG AGTAGCTGGG ATTACAGGCA CGCTTCATCA 480
TGCCCGGCTA ATTTTTTTGT ATTTTTAGTG GAGATGGGGG TTTCGCCATG TTGGTCAGGC 540
TGGTCTCGAA CTCCTGACCC CGTGATTCGC CCACCTCTGC CTCCCAAAGT GCTGGGATTA 600
CAGGTGTGAG CCACCGCACC CAGCTGAATC TCAGCTTTAA AGGGGAACTT GGAAGCGTGT 660
GGCCACTGAA CTCTGAAGAG CCTTCCATTT CCTGTTTGCA AATGAAGCCC CAGGATCCAG 720
ATGTACTGCT TGTGTCTTAG ACCATGAAAG CCTTAGCAAG ACTGATCTCC AGAACAGTCA 780
CGACTGCGGG AGAAAGCCAA GCTCATTTGC AATAGCAGCG TCCACCAGAG CACTTTGCAG 840
AGCCTGAATG CTGTGGAAAC TCTGGGTCTC GTTCCTGTCA CTCACTCAGA AAGAGCCAGA 900
GTGAAAAGAT GTGAACTGTG CGTCCTGCAT GTGGAAATTG CCTTTCAGCA GAGTCCCTGC 960
CCGTGGAGTA ACTCGGCTTT CAGGGCTAGA TCTTGACAGG CGCCACACTG GTTGTATTTG 1020
GAGTTGGCTC TTCCTTTAAG TAGCTGCGGG TCCCCAACCG TGGAGGGCTG GCAGTCTTGT 1080
CTCCCCGTAG GTGGCTTAGG 1100
|
