Variant report

Variant	rs775096
Chromosome Location	chr20:16004607-16004608
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 21 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:15)

rs_ID	r²[population]
rs1339255	1.00[CEU][hapmap]
rs175780	1.00[CEU][hapmap]
rs4814418	1.00[CEU][hapmap]
rs4814421	1.00[CEU][hapmap]
rs6034337	1.00[CEU][hapmap]
rs6043602	1.00[CEU][hapmap]
rs6043624	1.00[CEU][hapmap]
rs6043627	1.00[CEU][hapmap]
rs6043632	1.00[CEU][hapmap]
rs6043638	1.00[CEU][hapmap]
rs6080022	1.00[CEU][hapmap]
rs717146	1.00[CEU][hapmap]
rs7352227	1.00[CEU][hapmap]
rs775094	1.00[CEU][hapmap]
rs811343	1.00[CEU][hapmap]

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	nsv869328	chr20:15325423-16213898	Flanking Active TSS Enhancers ZNF genes & repeats Weak transcription Bivalent Enhancer Active TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
2	esv3447866	chr20:15799286-16115291	Enhancers Genic enhancers Bivalent Enhancer Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS Strong transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
3	nsv1065548	chr20:15971797-16023086	Enhancers Weak transcription Bivalent Enhancer Strong transcription Genic enhancers ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
4	nsv1059778	chr20:15999519-16165895	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Active TSS	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
5	nsv544207	chr20:15999519-16165895	Weak transcription Bivalent Enhancer Enhancers ZNF genes & repeats Active TSS Flanking Active TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
6	nsv585649	chr20:16004320-16066764	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Strong transcription Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr20:15998400-16012000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
2	chr20:16002200-16005800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr20:16002400-16005000	Weak transcription	HSMM	muscle
4	chr20:16003600-16007800	Weak transcription	Fetal Brain Female	brain
5	chr20:16004200-16006000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
6	chr20:16004200-16006200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
7	chr20:16004200-16008800	Enhancers	Primary B cells from peripheral blood	blood
8	chr20:16004400-16004800	Enhancers	H1 Cell Line	embryonic stem cell
9	chr20:16004400-16005000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
10	chr20:16004400-16005000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
11	chr20:16004400-16006200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
12	chr20:16004400-16006200	Enhancers	Primary B cells from cord blood	blood
13	chr20:16004400-16006400	Enhancers	HSMMtube	muscle
14	chr20:16004600-16005200	Enhancers	Primary hematopoietic stem cells	blood
15	chr20:16004600-16005400	Enhancers	HUES64 Cell Line	embryonic stem cell
16	chr20:16004600-16006400	Enhancers	Muscle Satellite Cultured Cells	--
17	chr20:16004600-16006400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
18	chr20:16004600-16007200	Weak transcription	Brain Germinal Matrix	brain

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dbSNP/dbVar ID: rs12345 /nsv7879
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chromosomal regions: chr1:12345-34567

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