| Tag | Content |
|---|
EnhancerAtlas ID | HS052-11744 |
Organism | Homo sapiens |
Tissue/cell | Fibroblast_foreskin |
Coordinate | chr14:70353970-70355380 |
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 | chr14:70354923-70354934 | CATGAGTCACT | - | 6.14 | | OLIG2 | MA0678.1 | chr14:70354090-70354100 | ACCATATGGT | + | 6.02 | | OLIG2 | MA0678.1 | chr14:70354090-70354100 | ACCATATGGT | - | 6.02 |
|
| | 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 |
| GH14I069888 | chr14 | 70353970 | 70355470 |
|
Enhancer Sequence | AAAAAAAGTT TTTAGGACTA CATACAGCTA CAACAAAATG CTATGAAAAG CATAGTAAAG 60
TAATGATGGA TACAGATTCA GGGTGAAGTT AGGGTGAGGC AGGGGGATAG GATGGGTAAA 120
ACCATATGGT TGGTGTGGGT TGGTGTTGAT ACTCTACCTT TTTGGGGGAG AGGGAGGATG 180
GGCTAAAGGC ATTTGTCCAT TATTCAAGAT CTAATAGCTG ATAAAAAAGT GAGCCCTGCA 240
TAAACCAATG CTGAGTGTAT CATGAGCCAA AGATTAAAAT TAATTCAATT CTTTGCATGT 300
GAGGTCAAAC AAAAAGTCCC AGAGTAAGGG ACTCCTTTCT TGCCACCTTC TGCTTCCTCC 360
CCACCTTTCA AGATGTGCAT GTGGCTCTAT CTAAAATAAC CCCACTGGGG AGTGATTTTG 420
GCTTCTAGAC CCAGAGCAGA CCCAGGCCCT GGCATAAACG TCTGCATCAG GTGGCCTAAG 480
GGCTCATTTG TAAAGCTAAG CTGGCAGTGG GCAGTCTTCC CTTTTCCTTG CTCAGGGTGA 540
TTCACCCTGC AGAGTGGAAG TGTTCATGAG CTGATGCATG GGTCAGAAAC TTTATTTGCC 600
AGTGGGGCCT GTGGGTGGAG GTAGTGTCTG GACTAGGGGA AGGCCTGTTT CTAGTTTGAT 660
GCCTGTCTTT ATTCCAACCT CCCCTCACCG CCTTTTGCAG GAGCTGGGGG TGGGATGCAT 720
GGTCCTGCTT AGCAGGTACA GGGCACCCTT TCTCTCTGGG CCACATAGAG ATTTATTGTT 780
TAGGCAGCCA AGTCCTGGTA TTGCTGCTAG TGGTAGAGGA TGTCAGTGTG GAGGGCCCCC 840
TCCTTCCATG TTTGGGGAGG ACAAAGGTTG AGTTGCGGAT GAGAAATAAA TCGGAGCTGC 900
TTGTGAGGCC GCCAAACAGG GTTAGATTTG TACAGTATGT GCTCTGCATG GGTCATGAGT 960
CACTGAGAGG TTCAGAGATT GGATTGCCAT GAATCACTTC CAACTGTCCC CATGAAGACC 1020
CCAAAGCAAC ATAGGTGACT ATAGGGTTTT CTTTTGCATC CAACATCATT CGGAATTCAG 1080
TTGCTAGATC ACAAAATAAT CTTACCTTTG GCCACATCTA AGCTTGTTAG GTATGGAGCT 1140
CTGCATACTT CCTGGACGTC ACCTTGGTTG ATTTCAGCAT CCTTTTTTTG AGTCAGAATG 1200
GGGCAGCCTC TCTAAGACAG GAAAGGTAGC TCTCATCTCA GTAGAGCCTT TCCCACCACC 1260
AGGGAGCACT GGGACTGAGC AAAGTTCCAT GAGGTCAGGC ATAATGTGTT TTGAAACCTG 1320
ACAAATTATC TAGAGGTTTG AACAACTACG CCTCGCCTCC TTAAAATCTA TTTTACACTA 1380
CGGTGTTGAT TGGATTCTAT AAGATAAGGG 1410
|
