| Tag | Content |
|---|
EnhancerAtlas ID | HS154-18456 |
Organism | Homo sapiens |
Tissue/cell | Osteoblast |
Coordinate | chr5:178980560-178981650 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NR2F1 | MA0017.2 | chr5:178980916-178980929 | CAAAGGTCACCGG | + | 6.37 |
|
| | 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 |
| GH05I179553 | chr5 | 178980603 | 178981704 |
|
Enhancer Sequence | GATCACCTGA GGTCAGGAGT TCGAGACCAA CCTGGCCAAC ATGGTGAAAC CCTATCTCTA 60
CTAAAAAAAA AAGTACAAAA ATTAGCCGGG CTTGGTGGTA CGCACCTGTA ATCCCAGCTA 120
CTCAGGAGGC TGAGGCAGGA GAATTGCTTG AACATAAGAG GCGGAGTTTG CAGTGAGCCG 180
AGACCATTCC ACTGCAGTCC AGCCTGGGCA ACAGAACGAG ACTATCTCAA AAAATAATAA 240
TTAACTCAAT TTAAGGAAAG TATTAATAAC TACCACTCAA TCTAGCAAAA TGGTGACCAT 300
GGCTTACAAA GAGATGAAAT TTGGGGAACT GCTGGGTAGA GCCATGAGGC TGGTCCCAAA 360
GGTCACCGGG ATTTGAAGCC ATCAGGTAGG ACAGGAGCAG AGGTGGGAAA GGAAATGGGC 420
CAAGGGCGGC TCGCTCTGCA GCGACACAAG AAAAACAGGA TGGGAGAAAG ACAGTGACAC 480
CACTTCAGCC AGGGCCAGGC CCAAGGCTGA CTCATTCTCT TTCCCCACTG ATCTGCCTAC 540
ACAAGCAATG AGGACAGGCA GGACTTTCAG AGGGAGCAGT TTAGGAGCAG AGATTGAATG 600
TGAGCAGCAC TCTTGCTGGA TGATATTTTT TCAATGGTAG AAGCTAAAGG AAATGCTGCG 660
GAATATTTTG AATACTTGTT TTAAAATGTT GTCCCGGTCG GGTGCAGTGG CTCATGCCTG 720
TAATCCCAGC ACTTTGGAAG ACCGAGGTGG GTGAATCACC TGATGTTGGG AGTTTGAGAC 780
CAGCCTGACC AACATGGAGA AACCCCGTCT CTACTAAAAA TACAAAATTA GCCAGGCATG 840
GTGGCGTAGG CGTGTAATCC CAGCTATTCA GGAGGCTGAG GCAGGAGAAT CTCTTGAACC 900
TGGGGGGTGG AGGTTGCTGT GAGCCAAGAT CGCCGCATTG CACTTCAGCT AGGGCAACAA 960
GAGCAAAACT TTGTCTCAAA AAAAAAAAGA AAAGAAAAGT TTTCCCATGT GGGGTCTGGT 1020
ATGTGATTGT ATTGTCCATA GGTGTCCTGT TTGGTTTTGG GGGATTTTTT TTTAAGGTAA 1080
TAAGCGAACA 1090
|
