| Tag | Content |
|---|
EnhancerAtlas ID | HS187-10273 |
Organism | Homo sapiens |
Tissue/cell | Th1 |
Coordinate | chr17:29759920-29761050 |
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 | ATTGCTTGAT CTCAGGTGGA TCACTTGAGT CCAGGAGTTT GAGACCAGCC TGGCCAACAT 60
GGCGAAACCT CATCTCTACA AAAAATACAA AAAATTAGCC GGGCATTCTG GTGTGTGCCT 120
GTGGTCCCAG CTACCTGGGA GGCTAAGGTG GGAGGATCAC CTGAGCCCAG GAAGTTGAGG 180
CTGCAGTGAG CTGAGGTCAC GCCACTGCAC TCCAGCCTGG GTAACAGAGT AAGAACCTGT 240
CTCAAGAAAG AAAAAAATCT GAGACAGTGG CATAGGTCAC CAGCCAGGTG GACTTGCTAA 300
GGCCTCCCCA CTAGCTGCAG AGAGAATGCA GTCACTTCTG GAGTCCCAGG GTGTCTGCTT 360
ATCTGTGAAG GAAGCCATGG TTTCCTGTCT GCGGCTCAGA TCAAGTTTAG CCCTTTTCTG 420
TGGGGTGCCT ATGAGTCCTG GGAGGGTGGA ACGATGCAGG GTGAGGGATG AAGGGAACCA 480
AATACACGGT GCAGGGGGCA CAGAACACAG AAGGTGCCCA GGGAAGGTTT TCTGCGTGGA 540
TTTGACAATG GGCCACTGCA GGCTGCACCT GCCATGTGCC TGTGCCAGGC ATTTTGTCAG 600
GTCCCCCTCC CAGTTCAGTA CAACCTTGGG GCGTTTGGTT GGGATCTCAG GAGCGAGGCC 660
AGCCGTGTAC AGAGTCAGCA GGAACTGCAG CTGTCCTGCG GGCAGCCCTG TCCTGGACGT 720
CCCAGGGTCT GCAGGACACG GGGGGCGCCC AGCCTCGGAG GAATGGGTGT GTTTGCTTTC 780
TCCAGAGGCT GGCACAGTCG TTTGGAGTCC CTGCAAGCCA GGTGGGCAGC ACTGCCTTAG 840
GTCCCCTCCC CCAGGAAGGC CTCCTTCCTT CCTGTTGCCC CAGCCTGCCC TCTGTGTGTG 900
GGAATTAGTC CCAGAGGACA AGGGCCTCTT GCAGCTCCCT CCACAGTGCC TTGAGCTGAG 960
TTCCCCACCG CCTGGGCTCC ATCCCTGCCT TCCAGTGCTC AGCTGGCCTC CTGGAGCCTC 1020
GGGCCCCCAC CTCAGCCCTT CCCACCCTAT GCCCATTAGT CAGAAGCAGA GCAGCCGTCC 1080
CAGGCTGAGG CTCAACCCCT CACTGTCCCG TGTGTCTGCC TGTCTGCGCA 1130
|
