Variant report

Variant	rs11901995
Chromosome Location	chr2:12129918-12129919
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 15 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:13)

rs_ID	r²[population]
rs16858066	1.00[AMR][1000 genomes]
rs60406176	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6723216	1.00[AMR][1000 genomes]
rs6732821	1.00[AMR][1000 genomes]
rs6736659	1.00[AMR][1000 genomes]
rs6748351	1.00[AMR][1000 genomes]
rs6748733	1.00[AMR][1000 genomes]
rs73175452	1.00[AMR][1000 genomes]
rs73175470	1.00[AMR][1000 genomes]
rs73177640	1.00[AMR][1000 genomes]
rs73179831	1.00[AMR][1000 genomes]
rs7568754	1.00[AMR][1000 genomes]
rs7606301	1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1003899	chr2:11789374-12248081	Strong transcription Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	26 gene(s)	inside rSNPs	diseases
2	nsv580999	chr2:12119686-12134346	Flanking Active TSS Weak transcription Enhancers Bivalent/Poised TSS Bivalent Enhancer Active TSS ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:12125400-12134200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr2:12127000-12135600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr2:12129600-12130000	Bivalent Enhancer	Adipose Nuclei	Adipose
4	chr2:12129600-12130000	Enhancers	NHDF-Ad	bronchial
5	chr2:12129600-12130200	Enhancers	Fetal Muscle Leg	muscle
6	chr2:12129800-12130000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
7	chr2:12129800-12130000	Enhancers	Skeletal Muscle Male	skeletal muscle
8	chr2:12129800-12135200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin

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

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