| Tag | Content |
|---|
EnhancerAtlas ID | HS108-16568 |
Organism | Homo sapiens |
Tissue/cell | K562 |
Coordinate | chr17:29055380-29056850 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOSL1 | MA0477.1 | chr17:29055563-29055574 | CATGAGTCACC | - | 6.62 | | JUND | MA0491.1 | chr17:29055563-29055574 | CATGAGTCACC | - | 6.02 | | SPI1 | MA0080.4 | chr17:29055729-29055743 | GAAATGAGGAAGTT | + | 6.43 |
|
| | 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 |
| GH17I030727 | chr17 | 29054749 | 29056964 |
|
Enhancer Sequence | ATCGTGCCAC TGCACTCTAG CCTGGTGACA GAGTGAGACT CCGTCTCAAA AAAAAAAACA 60
AATTTCTAGA GACATGTTGC CCAGGCTGGA GTGCAGTGGC ACGATCATAG CTCACTGCAG 120
CCTTGAACTC CTGGGCTGAA GTGATCCACC CACCTTAGCC TCCCAAAGCA CTGGGATCAC 180
AGGCATGAGT CACCGTACAA ATCCAGCCAT TTTTACTTCC CCTAACCAGT TCCTCTGCTA 240
GGATGCCTGT TGCAGTGTGA AAGAAAGCGC TTGGAGACCC TGGGAGGGGA GTACTCCTCA 300
GCTTGGGGAC ACTGCCTCCA CTGAACCTTT CTGTGGCTGG ACAGTTGGAG AAATGAGGAA 360
GTTGAAATAA GGAAGCCACT CCCCATCCCC AAAGTAACAT GCTGGAAAAT GATCTGAAAG 420
TGACACCAGC CATGTCTAGT CACAGATGTG GGGGGAGATG CGGACGGGGG CTGGTGGCGG 480
CTGGGGGAGT AACACGCTGT AAAATGATCT GAAAGTGACA CCAGCCGTGT CTAGTCAGGG 540
ATGTGGGGGG AGATGCGGAT GGGGGCTGGA GGTGGCTGCG GGGGATTTAG TGAAGAAGCT 600
GGGGCAGTGG AGAGGGAGCT GGTATCAGGA GTGGGCATGA GAGGGGAAGC GGGCAGAGAG 660
CTACAGGGCT GGAGAGGGGG TGTTCAGGGC TGTCTTGCAG ATATTATCCT CCCATTTCCC 720
ATGTGAGGAG ACTGAGGTCT GGACCAGGTG TCCTGCCCTG TGGGGATCTT TATTTATTGA 780
GGGCCTGTGC CTATTTGTTT TATTTTATTT ATTTATTTTT GAGACAGTCT GGCTCTGTTG 840
CCCGGACTGG AGTGCAATGG CACAATCTAG CCTCACTGCA ACCTCTACCT CTCGGGTTCA 900
ACCAATTCTT GTGCCTCAGC CTCCCGAGTA GCTGGGATTA CAGGTATCTG CCACCACGCC 960
CGGCTAATTT TTTGGTATTT TTAGTAGAGA CGGGGTTTCA CCATGTTGGC CAGGGTGGTC 1020
TCGAACTCCT GACCTCTGGT GATCCACCCG CCTCGGCTTC CCAAAGTGCT GGGATTACAG 1080
GCATGAGCCA CTGTGCCCAG CCGTGTGCTG ATTTCTAAGG GCCTCTCTCA AGAAGCTCGT 1140
GTTGATAAAA AGGTAATTTC AGGTGCTCAC TTGAGAGCTG TGAATTAAAA ACAGGGAAAA 1200
GATGGCGGGT GAGGGCAGCA GGCGAGGACT GTTTTGTTTG CAGGGGGCCA GGGTAGGTCA 1260
CTCTGCTGCG GTGACCTTGC GGCTGAGCCC TGAACAATGA GCAGCCGCAG CCAACATGCA 1320
GGGATCCTGC TTGGGGGCTG GAACTGGAAT GTTGAATGTT TCAGGAACAG GAGGGAGGAC 1380
AGAATGGGGC TTGGAGAGCT TGGTGGCACC AGTTCACCCA CAGCCTCTGG GCTCTAGTGA 1440
GGAAATGAGA CCCCAGCAGA GACCAGGGGG 1470
|
