Variant report

Variant	rs17012968
Chromosome Location	chr2:33636833-33636834
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 6 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:2)

rs_ID	r²[population]
rs17012979	0.84[AFR][1000 genomes]
rs17038533	0.97[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1005435	chr2:33136117-33747159	Weak transcription Strong transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	22 gene(s)	inside rSNPs	diseases
2	nsv535624	chr2:33136117-33747159	Weak transcription Enhancers Genic enhancers Flanking Active TSS Bivalent Enhancer Strong transcription ZNF genes & repeats Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	22 gene(s)	inside rSNPs	diseases
3	nsv1012967	chr2:33533340-33638312	Enhancers Weak transcription ZNF genes & repeats Genic enhancers Strong transcription Bivalent Enhancer Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region	5 gene(s)	inside rSNPs	diseases
4	nsv535627	chr2:33533340-33638312	Enhancers Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Active TSS Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	5 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:18 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:33629600-33641800	Weak transcription	Right Atrium	heart
2	chr2:33631200-33640200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
3	chr2:33631400-33637000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
4	chr2:33632600-33637200	Weak transcription	HSMMtube	muscle
5	chr2:33633800-33637000	Weak transcription	Fetal Kidney	kidney
6	chr2:33634000-33645000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
7	chr2:33635200-33637000	Weak transcription	HSMM	muscle
8	chr2:33636400-33638600	Enhancers	Muscle Satellite Cultured Cells	--
9	chr2:33636800-33637000	Enhancers	A549	lung
10	chr2:33636800-33637000	Enhancers	HMEC	breast
11	chr2:33636800-33637400	Enhancers	NH-A	brain
12	chr2:33636800-33637600	Enhancers	NHLF	lung
13	chr2:33636800-33637800	Enhancers	Ovary	ovary
14	chr2:33636800-33638200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
15	chr2:33636800-33638200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
16	chr2:33636800-33638200	Enhancers	NHDF-Ad	bronchial
17	chr2:33636800-33638200	Enhancers	Osteobl	bone
18	chr2:33636800-33638400	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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