Variant report

Variant	rs16936137
Chromosome Location	chr11:19115786-19115787
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 14 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:12)

rs_ID	r²[population]
rs10500838	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10500840	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10833055	0.94[YRI][hapmap]
rs16924998	1.00[AMR][1000 genomes]
rs16936120	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs16936124	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs16936126	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs16936127	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs16936146	0.86[YRI][hapmap];0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs41420346	0.87[AFR][1000 genomes]
rs59309964	1.00[AMR][1000 genomes]
rs60139631	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	nsv1040805	chr11:19037871-19892803	Enhancers Bivalent Enhancer Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	25 gene(s)	inside rSNPs	diseases
2	nsv540957	chr11:19037871-19892803	Active TSS Weak transcription Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS Genic enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	25 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:17 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:19115000-19116200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
2	chr11:19115000-19116200	Enhancers	Muscle Satellite Cultured Cells	--
3	chr11:19115000-19116200	Enhancers	Rectal Mucosa Donor 31	rectum
4	chr11:19115200-19116000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
5	chr11:19115200-19116000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
6	chr11:19115200-19116000	Enhancers	Fetal Intestine Large	intestine
7	chr11:19115200-19116000	Enhancers	HMEC	breast
8	chr11:19115200-19116000	Enhancers	NH-A	brain
9	chr11:19115200-19116000	Enhancers	Osteobl	bone
10	chr11:19115200-19116800	Enhancers	Fetal Intestine Small	intestine
11	chr11:19115400-19116200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
12	chr11:19115600-19115800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
13	chr11:19115600-19115800	Enhancers	Pancreas	Pancrea
14	chr11:19115600-19115800	Enhancers	HUVEC	blood vessel
15	chr11:19115600-19116000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
16	chr11:19115600-19116000	Enhancers	HSMM	muscle
17	chr11:19115600-19116000	Enhancers	HSMMtube	muscle

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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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