| Tag | Content |
|---|
EnhancerAtlas ID | HS187-10281 |
Organism | Homo sapiens |
Tissue/cell | Th1 |
Coordinate | chr17:30406370-30407820 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| RFX1 | MA0509.2 | chr17:30406933-30406949 | CGTTGCCATAACAACT | + | 6.71 | | RFX1 | MA0509.2 | chr17:30406933-30406949 | CGTTGCCATAACAACT | - | 6.71 | | RFX2 | MA0600.2 | chr17:30406933-30406949 | CGTTGCCATAACAACT | - | 6.57 | | RFX2 | MA0600.2 | chr17:30406933-30406949 | CGTTGCCATAACAACT | + | 6.71 | | RFX5 | MA0510.2 | chr17:30406933-30406949 | CGTTGCCATAACAACT | - | 6.22 | | RFX5 | MA0510.2 | chr17:30406933-30406949 | CGTTGCCATAACAACT | + | 6.51 |
|
| | 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 |
| GH17I032079 | chr17 | 30406421 | 30407485 |
|
Enhancer Sequence | TGGATTGGTT GAGAGATCAC CGTATGCCAG AAGTTGCTTT AAGCATTTTG CATGTATTAA 60
TCCATTTTAC ACCTCACAAT ATCGCTACCA AGTAGAAACG ATTATCTCGA TTTTGTAAAA 120
GGTGAAACAG GAAAAAACCA CTAGAGCAGA GCTGGCAGAC CCTCAACCTT CTTTTCCTTC 180
TGACTCCAAA TGACAGACAG CATTCTTTCC ATCTCTCACC TCCTCATGCC TCCTGTGGAA 240
AAAATGAATG AACAGATGAG AAAAGTTGGA GCTGGAGAAA GACCGTGTTC CTCGTGTTCT 300
GTGAGACCTG GGAAGGCTGC TAAAACCCAG GGAGCAGGAG TTCTCCTCCC TCCATCCTTA 360
TCCACAGTCT GGGTCCCATC CAGACCCTCC TCTCCAAACC GGGGGTTTGC GACAAAGCAG 420
GTGAGGGAGG CATTTCATTC CAGAGCAGAA GAAGGGGGTT CCTCCCCCAT CCCACTCCCG 480
TTTCATTTTT AAGGGGAAAA GCAGCTCCCC ATACGGTGAG GCAATGAGGC GGACCAGCAG 540
GTTCCTGGGG ATCTCCGCAG CCCCGTTGCC ATAACAACTG AACTCACTCG CAGCCTCTGA 600
TAGGGGAGTC AGCTGGAACC ACAGCTTGGG CAGGAAACGG ATGAGGGAGT AGGAAAGAAA 660
CTTCAAGATC AACCACTGGC CCTCACACCG AGCTGCGCAC ACCCCAAGGC CAAGTGAGGC 720
TGGAAACCCT TGTTGTCCTT GGGAAATGGG GGAGGGCACT GGTACCCCTG GGACCTCCCT 780
CCTGAATCTG GGCAGGTTTA AACATTTTTT TTCCAACTTT GGAAGACAGT TGTACAACCT 840
CGAAGGAGAG GAGGTGTCAG GATTCACAAA GCGTATGGAT CACACATGGC TCTAGGGGAC 900
ATTCTCTTTG CTCTGTTTTA TTTTTATTGT ATATTTTATT CTTTTATTTT GCGATAGGGT 960
CTTGCTCTAT TGCCCAGGCT GGAGTCCAGT GGCATGACCA CACCTTACTG CAGCCTCAAA 1020
TTACTGGACT GAGGTGATCC TCCTGCCTCA GCCATGCGAG TAGCTGGGAC TACAGACATG 1080
CACCACCACA CCTGGCTAAT TTTTAAAATA TATATGTTTT TGTAGAGATA GGGTCCTGCT 1140
ACATTGCCCA GGCTGGTCTC AAACTCCTGG CTTCAAGTGA TCCTCCTGCT TTGGCCTCCC 1200
AAAGTGTTGG GATTATAGGC ATGAGCCACT GCATCCAGCA TCATTTCTTT TCATTATTAT 1260
TATGATTATT ATTTTGAGAT GGAGTCTCGC TCTGTCACCC AGGCTGTAGT GGAGTGGTGT 1320
GACCTCGGCT CACTGCAACC TCCACCTCCC AGGTTCAAGT GATTCTCCTG CCTCAGCCTC 1380
CTGAGGAGTT GCGATTACAG GTACCCTCCA CAATGCCTGG CTAATTTTTT TTTCTTTTTG 1440
AGACGGAGTT 1450
|
