Variant report

Variant	rs61519866
Chromosome Location	chr12:60466315-60466316
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 13 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:7)

rs_ID	r²[population]
rs74095924	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74095928	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74095929	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74095931	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74095932	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74095934	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74098525	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv869425	chr12:59746898-60479741	Weak transcription Enhancers ZNF genes & repeats Active TSS Strong transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	22 gene(s)	inside rSNPs	diseases
2	nsv899136	chr12:60373244-60483607	Enhancers Strong transcription Weak transcription ZNF genes & repeats Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
3	nsv559103	chr12:60383069-60483607	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
4	nsv1048137	chr12:60432594-60515455	Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Strong transcription	TF binding region Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
5	nsv428591	chr12:60446360-60631044	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
6	nsv427913	chr12:60462443-60569344	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Strong transcription Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:12 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:60464000-60467400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
2	chr12:60464000-60467400	Enhancers	NHEK	skin
3	chr12:60464200-60466800	Enhancers	HUVEC	blood vessel
4	chr12:60465000-60467400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
5	chr12:60465200-60467000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
6	chr12:60465200-60467000	Enhancers	HMEC	breast
7	chr12:60465600-60467000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
8	chr12:60465800-60467600	Enhancers	ES-I3 Cell Line	embryonic stem cell
9	chr12:60466000-60466400	Enhancers	Aorta	Aorta
10	chr12:60466000-60467400	Enhancers	NH-A	brain
11	chr12:60466200-60467400	Enhancers	HUES48 Cell Line	embryonic stem cell
12	chr12:60466200-60467400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow

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Input of quick search could be:

dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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