Variant report

Variant	rs10873941
Chromosome Location	chr1:77902981-77902982
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 10 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:1)

rs_ID	r²[population]
rs55924989	1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:9 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1005183	chr1:77728990-77949309	Weak transcription Flanking Active TSS Enhancers Strong transcription Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
2	nsv535010	chr1:77728990-77949309	Bivalent Enhancer Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
3	nsv932557	chr1:77730247-77958687	Flanking Active TSS Enhancers Strong transcription Weak transcription ZNF genes & repeats Bivalent Enhancer Genic enhancers Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
4	nsv1003714	chr1:77756861-77949309	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers Bivalent Enhancer Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
5	nsv470719	chr1:77774413-78269207	Weak transcription Enhancers Flanking Active TSS Strong transcription Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	34 gene(s)	inside rSNPs	diseases
6	nsv546591	chr1:77774413-78269207	Active TSS Weak transcription Flanking Active TSS Enhancers Genic enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	34 gene(s)	inside rSNPs	diseases
7	esv1848735	chr1:77885282-77918347	Weak transcription ZNF genes & repeats Strong transcription Enhancers Flanking Active TSS Active TSS Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
8	nsv871605	chr1:77889505-77918347	Weak transcription Enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Active TSS Bivalent Enhancer	Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
9	nsv521371	chr1:77899640-77912969	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription Genic enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs10873941	DNAJB4	cis	parietal	SCAN

Chromatin state (count:32 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:77872200-77913800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
2	chr1:77893800-77903600	Weak transcription	Brain Hippocampus Middle	brain
3	chr1:77894200-77905200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
4	chr1:77894200-77912400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
5	chr1:77894200-77912600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
6	chr1:77897000-77903400	Weak transcription	HSMMtube	muscle
7	chr1:77897400-77903000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
8	chr1:77897800-77903400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
9	chr1:77899200-77903400	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
10	chr1:77900200-77913600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
11	chr1:77900800-77904800	Enhancers	Primary T helper naive cells fromperipheralblood	blood
12	chr1:77901200-77903400	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
13	chr1:77901200-77904200	Enhancers	Primary T cells from cord blood	blood
14	chr1:77901400-77903800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
15	chr1:77901400-77904200	Weak transcription	Primary T cells fromperipheralblood	blood
16	chr1:77901400-77904200	Weak transcription	Primary hematopoietic stem cells	blood
17	chr1:77901800-77903200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
18	chr1:77902000-77903000	Weak transcription	Primary T helper cells PMA-I stimulated	--
19	chr1:77902200-77904000	Enhancers	NHDF-Ad	bronchial
20	chr1:77902400-77903800	Enhancers	Primary T killer naive cells fromperipheralblood	blood
21	chr1:77902400-77904000	Enhancers	Muscle Satellite Cultured Cells	--
22	chr1:77902400-77904200	Enhancers	Primary T helper naive cells from peripheral blood	blood
23	chr1:77902600-77903400	Active TSS	A549	lung
24	chr1:77902600-77903800	Enhancers	Brain Angular Gyrus	brain
25	chr1:77902600-77903800	Enhancers	Osteobl	bone
26	chr1:77902600-77904000	Enhancers	Rectal Smooth Muscle	rectum
27	chr1:77902600-77904200	Enhancers	Primary T killer memory cells from peripheral blood	blood
28	chr1:77902600-77904400	Active TSS	NHLF	lung
29	chr1:77902800-77903000	Active TSS	Primary T helper cells fromperipheralblood	blood
30	chr1:77902800-77903200	Weak transcription	HSMM	muscle
31	chr1:77902800-77904200	Enhancers	Brain Cingulate Gyrus	brain
32	chr1:77902800-77904400	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow

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