Variant report

Variant	rs41527748
Chromosome Location	chr4:86648745-86648746
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr4:86636846..86639460-chr4:86646994..86650013,3	K562	blood:

Extended variants
information (count: 50 )
Associated
traits (count: 2 )

rSNPs within LD-proxies of this variant (count:45)

rs_ID	r²[population]
rs10012090	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.83[MEX][hapmap];0.95[ASN][1000 genomes]
rs10516755	0.85[CHB][hapmap];1.00[JPT][hapmap];0.95[ASN][1000 genomes]
rs11736641	1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[ASN][1000 genomes]
rs11937419	1.00[ASN][1000 genomes]
rs13102580	1.00[ASN][1000 genomes]
rs13105921	0.82[CHB][hapmap];1.00[JPT][hapmap]
rs13111293	1.00[CHB][hapmap];0.89[CHD][hapmap];1.00[JPT][hapmap];0.84[MEX][hapmap];0.95[ASN][1000 genomes]
rs13111662	1.00[CHB][hapmap];0.88[CHD][hapmap];1.00[JPT][hapmap];0.83[MEX][hapmap];0.95[ASN][1000 genomes]
rs13112030	0.86[ASN][1000 genomes]
rs13113783	0.95[ASN][1000 genomes]
rs13127274	1.00[ASN][1000 genomes]
rs13137008	1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[ASN][1000 genomes]
rs13150566	0.95[ASN][1000 genomes]
rs1482093	1.00[ASN][1000 genomes]
rs1482094	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.84[MEX][hapmap];1.00[ASN][1000 genomes]
rs17010755	1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[ASN][1000 genomes]
rs17010812	0.93[ASN][1000 genomes]
rs17010816	0.93[ASN][1000 genomes]
rs17010847	0.91[ASN][1000 genomes]
rs2062097	1.00[ASN][1000 genomes]
rs2062098	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.84[MEX][hapmap];1.00[ASN][1000 genomes]
rs2198328	1.00[CHB][hapmap];0.89[CHD][hapmap];1.00[JPT][hapmap];0.84[MEX][hapmap];1.00[ASN][1000 genomes]
rs2601855	1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[ASN][1000 genomes]
rs2601860	0.92[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2601861	1.00[ASN][1000 genomes]
rs2624021	1.00[ASN][1000 genomes]
rs28490560	0.91[ASN][1000 genomes]
rs2869377	1.00[ASN][1000 genomes]
rs2869379	1.00[ASN][1000 genomes]
rs2869380	1.00[ASN][1000 genomes]
rs2869384	0.93[ASN][1000 genomes]
rs343849	1.00[CHB][hapmap];0.89[CHD][hapmap];1.00[JPT][hapmap];0.84[MEX][hapmap];1.00[ASN][1000 genomes]
rs343856	1.00[ASN][1000 genomes]
rs343860	0.82[CHB][hapmap];0.88[CHD][hapmap];0.80[MEX][hapmap];0.95[ASN][1000 genomes]
rs34422670	0.93[ASN][1000 genomes]
rs34949750	0.95[ASN][1000 genomes]
rs4302455	0.96[ASN][1000 genomes]
rs4507354	1.00[ASN][1000 genomes]
rs6813799	1.00[ASN][1000 genomes]
rs7658797	0.82[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.84[MEX][hapmap];0.95[ASN][1000 genomes]
rs7660252	0.91[ASN][1000 genomes]
rs7660702	1.00[JPT][hapmap];0.87[MEX][hapmap];1.00[ASN][1000 genomes]
rs7677114	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.84[MEX][hapmap];0.88[MKK][hapmap];1.00[ASN][1000 genomes]
rs7692808	1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[ASN][1000 genomes]
rs994285	1.00[CHB][hapmap];0.89[CHD][hapmap];1.00[JPT][hapmap];0.84[MEX][hapmap];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv461566	chr4:85988032-86725502	Weak transcription Enhancers Flanking Active TSS Strong transcription ZNF genes & repeats Active TSS Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	5 gene(s)	inside rSNPs	diseases
2	nsv594747	chr4:85988032-86725502	Enhancers Active TSS Weak transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	5 gene(s)	inside rSNPs	diseases
3	nsv470048	chr4:85998783-86720838	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Genic enhancers Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	5 gene(s)	inside rSNPs	diseases
4	esv3450999	chr4:86485840-86773745	Enhancers Weak transcription Genic enhancers Active TSS Flanking Active TSS ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region miRNA	2 gene(s)	inside rSNPs	diseases
5	nsv829999	chr4:86500257-86666019	Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats Genic enhancers Strong transcription Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region miRNA	2 gene(s)	inside rSNPs	diseases

mRNA abundance (count:2)

SNP	Gene	Cis/trans	Tissue	Source
rs41527748	C4orf19	trans	cerebellum	SCAN
rs41527748	CDS1	cis	parietal	SCAN

Chromatin state (count:39 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:86644000-86650200	Enhancers	NHDF-Ad	bronchial
2	chr4:86645000-86650200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
3	chr4:86646000-86649000	Enhancers	Primary B cells from peripheral blood	blood
4	chr4:86646400-86649000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
5	chr4:86646800-86649400	Weak transcription	Fetal Kidney	kidney
6	chr4:86647000-86649400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
7	chr4:86647000-86653200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
8	chr4:86647000-86655400	Weak transcription	Brain Angular Gyrus	brain
9	chr4:86647200-86653200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
10	chr4:86647200-86658200	Weak transcription	Brain Inferior Temporal Lobe	brain
11	chr4:86647400-86649000	Enhancers	Primary hematopoietic stem cells short term culture	blood
12	chr4:86647400-86652400	Weak transcription	Stomach Mucosa	stomach
13	chr4:86647400-86653200	Weak transcription	Fetal Heart	heart
14	chr4:86647600-86649200	Weak transcription	Rectal Mucosa Donor 31	rectum
15	chr4:86647600-86649800	Weak transcription	HSMMtube	muscle
16	chr4:86647600-86652000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
17	chr4:86647600-86653400	Weak transcription	Fetal Lung	lung
18	chr4:86647800-86649400	Weak transcription	HSMM	muscle
19	chr4:86647800-86649800	Weak transcription	Muscle Satellite Cultured Cells	--
20	chr4:86647800-86651000	Weak transcription	Brain Hippocampus Middle	brain
21	chr4:86647800-86653200	Weak transcription	Brain Cingulate Gyrus	brain
22	chr4:86647800-86654600	Weak transcription	Colon Smooth Muscle	Colon
23	chr4:86647800-86655600	Weak transcription	Small Intestine	intestine
24	chr4:86647800-86656600	Weak transcription	Brain Anterior Caudate	brain
25	chr4:86647800-86656600	Weak transcription	Sigmoid Colon	Sigmoid Colon
26	chr4:86647800-86662600	Weak transcription	Left Ventricle	heart
27	chr4:86647800-86662600	Weak transcription	Spleen	Spleen
28	chr4:86648000-86649000	Enhancers	K562	blood
29	chr4:86648000-86650000	Weak transcription	Rectal Smooth Muscle	rectum
30	chr4:86648000-86650200	Enhancers	Primary neutrophils fromperipheralblood	blood
31	chr4:86648000-86652800	Weak transcription	GM12878-XiMat	blood
32	chr4:86648000-86654800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
33	chr4:86648000-86655200	Weak transcription	Primary hematopoietic stem cells	blood
34	chr4:86648200-86649600	Weak transcription	Adipose Nuclei	Adipose
35	chr4:86648200-86654600	Weak transcription	Primary B cells from cord blood	blood
36	chr4:86648400-86648800	Weak transcription	Fetal Muscle Leg	muscle
37	chr4:86648400-86648800	Weak transcription	Right Atrium	heart
38	chr4:86648400-86650200	Enhancers	Breast Myoepithelial Primary Cells	Breast
39	chr4:86648400-86662600	Weak transcription	Pancreas	Pancrea

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