Variant report

Variant	rs2514144
Chromosome Location	chr11:83691250-83691251
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 36 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:32)

rs_ID	r²[population]
rs1160817	1.00[CEU][hapmap]
rs1160818	1.00[CEU][hapmap]
rs1304480	1.00[CEU][hapmap]
rs1384748	1.00[CEU][hapmap]
rs1471687	1.00[CEU][hapmap]
rs1483387	1.00[CEU][hapmap]
rs1483388	1.00[CEU][hapmap]
rs1584853	1.00[CEU][hapmap]
rs1584854	1.00[CEU][hapmap]
rs1586143	1.00[CEU][hapmap]
rs1598073	1.00[CEU][hapmap]
rs1599914	1.00[CEU][hapmap]
rs1601094	1.00[CEU][hapmap]
rs1601096	1.00[CEU][hapmap]
rs1817515	1.00[CEU][hapmap]
rs2086741	1.00[CEU][hapmap]
rs2170707	1.00[CEU][hapmap]
rs2220085	1.00[CEU][hapmap]
rs2449575	1.00[CEU][hapmap]
rs2449592	1.00[CEU][hapmap]
rs2449594	1.00[CEU][hapmap]
rs2514146	1.00[CEU][hapmap]
rs2514165	1.00[CEU][hapmap]
rs2514166	1.00[CEU][hapmap]
rs2514167	1.00[CEU][hapmap]
rs2514171	1.00[CEU][hapmap]
rs2853026	1.00[CEU][hapmap]
rs790348	1.00[CEU][hapmap]
rs790351	1.00[CEU][hapmap]
rs790367	1.00[CEU][hapmap]
rs790372	1.00[CEU][hapmap]
rs7933909	1.00[CEU][hapmap]

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	nsv898025	chr11:83658909-83796678	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Genic enhancers	Chromatin interactive region	n/a	inside rSNPs	n/a
2	nsv1039924	chr11:83662904-83993497	Enhancers Active TSS Weak transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
3	nsv541102	chr11:83662904-83993497	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
4	nsv898026	chr11:83685801-83789540	Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	n/a	inside rSNPs	n/a

No data

Chromatin state (count:10 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:83683800-83692000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
2	chr11:83687600-83693000	Weak transcription	Brain Angular Gyrus	brain
3	chr11:83688400-83692000	Weak transcription	Brain Anterior Caudate	brain
4	chr11:83689800-83692200	Enhancers	Fetal Heart	heart
5	chr11:83690400-83691400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr11:83690400-83691600	Enhancers	Brain Hippocampus Middle	brain
7	chr11:83690600-83691400	Enhancers	HUES6 Cell Line	embryonic stem cell
8	chr11:83690600-83691600	Enhancers	Brain Cingulate Gyrus	brain
9	chr11:83690600-83692200	Enhancers	Brain Inferior Temporal Lobe	brain
10	chr11:83690600-83692200	Enhancers	Brain Substantia Nigra	brain

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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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