| Tag | Content |
|---|
EnhancerAtlas ID | HS051-11565 |
Organism | Homo sapiens |
Tissue/cell | Fetal_thymus |
Coordinate | chr17:29760000-29761050 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Myog | MA0500.1 | chr17:29760604-29760615 | CTGCAGCTGTC | - | 6.62 | | Tcf12 | MA0521.1 | chr17:29760604-29760615 | CTGCAGCTGTC | - | 6.14 |
|
| | 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 |
| GH17I031433 | chr17 | 29760221 | 29760350 |
|
Enhancer Sequence | AAAAATACAA AAAATTAGCC GGGCATTCTG GTGTGTGCCT GTGGTCCCAG CTACCTGGGA 60
GGCTAAGGTG GGAGGATCAC CTGAGCCCAG GAAGTTGAGG CTGCAGTGAG CTGAGGTCAC 120
GCCACTGCAC TCCAGCCTGG GTAACAGAGT AAGAACCTGT CTCAAGAAAG AAAAAAATCT 180
GAGACAGTGG CATAGGTCAC CAGCCAGGTG GACTTGCTAA GGCCTCCCCA CTAGCTGCAG 240
AGAGAATGCA GTCACTTCTG GAGTCCCAGG GTGTCTGCTT ATCTGTGAAG GAAGCCATGG 300
TTTCCTGTCT GCGGCTCAGA TCAAGTTTAG CCCTTTTCTG TGGGGTGCCT ATGAGTCCTG 360
GGAGGGTGGA ACGATGCAGG GTGAGGGATG AAGGGAACCA AATACACGGT GCAGGGGGCA 420
CAGAACACAG AAGGTGCCCA GGGAAGGTTT TCTGCGTGGA TTTGACAATG GGCCACTGCA 480
GGCTGCACCT GCCATGTGCC TGTGCCAGGC ATTTTGTCAG GTCCCCCTCC CAGTTCAGTA 540
CAACCTTGGG GCGTTTGGTT GGGATCTCAG GAGCGAGGCC AGCCGTGTAC AGAGTCAGCA 600
GGAACTGCAG CTGTCCTGCG GGCAGCCCTG TCCTGGACGT CCCAGGGTCT GCAGGACACG 660
GGGGGCGCCC AGCCTCGGAG GAATGGGTGT GTTTGCTTTC TCCAGAGGCT GGCACAGTCG 720
TTTGGAGTCC CTGCAAGCCA GGTGGGCAGC ACTGCCTTAG GTCCCCTCCC CCAGGAAGGC 780
CTCCTTCCTT CCTGTTGCCC CAGCCTGCCC TCTGTGTGTG GGAATTAGTC CCAGAGGACA 840
AGGGCCTCTT GCAGCTCCCT CCACAGTGCC TTGAGCTGAG TTCCCCACCG CCTGGGCTCC 900
ATCCCTGCCT TCCAGTGCTC AGCTGGCCTC CTGGAGCCTC GGGCCCCCAC CTCAGCCCTT 960
CCCACCCTAT GCCCATTAGT CAGAAGCAGA GCAGCCGTCC CAGGCTGAGG CTCAACCCCT 1020
CACTGTCCCG TGTGTCTGCC TGTCTGCGCA 1050
|
