Variant report

Variant	rs6854895
Chromosome Location	chr4:78851940-78851941
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr4:78849261..78852545-chr4:78852890..78855940,3	K562	blood:

Extended variants
information (count: 62 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:51)

rs_ID	r²[population]
rs10033527	0.95[CEU][hapmap];0.91[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.87[AMR][1000 genomes];0.86[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs10033613	0.87[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs1021824	0.90[AMR][1000 genomes];0.90[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs1021826	0.88[AMR][1000 genomes];0.90[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs11097938	0.82[CHB][hapmap];1.00[JPT][hapmap]
rs11729215	0.86[CHB][hapmap];1.00[JPT][hapmap]
rs12641050	0.82[ASN][1000 genomes]
rs12645742	0.82[CHB][hapmap];1.00[JPT][hapmap]
rs13101418	1.00[CEU][hapmap];0.95[CHB][hapmap];0.97[GIH][hapmap];0.94[JPT][hapmap];0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs13101987	0.82[CHB][hapmap];1.00[JPT][hapmap]
rs13103035	0.81[CHB][hapmap];1.00[JPT][hapmap]
rs13103523	1.00[JPT][hapmap]
rs13106067	1.00[CEU][hapmap];0.91[CHB][hapmap];1.00[JPT][hapmap];0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs13114091	0.82[ASN][1000 genomes]
rs13120272	1.00[JPT][hapmap]
rs16996915	0.86[CHB][hapmap];1.00[JPT][hapmap]
rs17002849	0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2088992	0.84[CEU][hapmap];0.82[CHB][hapmap];0.89[JPT][hapmap]
rs28404443	0.87[AMR][1000 genomes];0.86[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs34459497	0.82[EUR][1000 genomes]
rs34751953	0.85[AMR][1000 genomes];0.82[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs34850103	0.82[ASN][1000 genomes]
rs35648590	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs35979107	0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs4453957	0.87[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs4571357	0.88[AMR][1000 genomes];0.93[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs4577601	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];0.94[GIH][hapmap];1.00[JPT][hapmap];0.96[MKK][hapmap];1.00[YRI][hapmap];0.88[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4859509	0.95[CEU][hapmap];0.91[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.87[AMR][1000 genomes];0.86[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs4859511	0.95[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.87[AMR][1000 genomes];0.86[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs4859877	0.86[CHB][hapmap];1.00[JPT][hapmap]
rs4859879	0.82[CHB][hapmap];1.00[JPT][hapmap]
rs4859888	0.87[AMR][1000 genomes];0.86[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs4859889	0.84[ASW][hapmap];1.00[CEU][hapmap];0.95[CHB][hapmap];0.94[GIH][hapmap];1.00[JPT][hapmap];0.81[MKK][hapmap];1.00[YRI][hapmap];0.92[AMR][1000 genomes];0.97[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs62302728	0.99[AMR][1000 genomes];0.96[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs62302732	0.93[AMR][1000 genomes];0.96[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs6533282	0.95[CEU][hapmap];0.85[CHB][hapmap];0.93[JPT][hapmap];0.87[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs6533291	0.87[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs6533344	1.00[CEU][hapmap];0.91[CHB][hapmap];0.94[GIH][hapmap];1.00[JPT][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6533345	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs66825464	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6811736	0.86[CEU][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6814912	1.00[CEU][hapmap];0.91[CHB][hapmap];0.93[JPT][hapmap];0.99[AMR][1000 genomes];0.96[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs6845998	0.82[ASN][1000 genomes]
rs6848029	0.95[CEU][hapmap];0.91[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.87[AMR][1000 genomes];0.86[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs7670157	0.91[CHB][hapmap];0.89[JPT][hapmap];0.87[AMR][1000 genomes];0.86[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs7675009	0.84[ASW][hapmap];0.81[CEU][hapmap];0.86[CHB][hapmap];0.91[GIH][hapmap];1.00[JPT][hapmap]
rs7676660	0.84[AMR][1000 genomes];0.86[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs7695874	0.81[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs7698627	0.95[CEU][hapmap];0.86[CHB][hapmap];0.91[GIH][hapmap];1.00[JPT][hapmap];0.87[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs7698629	0.83[AMR][1000 genomes];0.86[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs905376	0.95[CEU][hapmap];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.94[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:11 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv879501	chr4:78647634-78866007	Active TSS Flanking Active TSS Strong transcription Weak transcription Enhancers ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	12 gene(s)	inside rSNPs	diseases
2	esv2752050	chr4:78693311-78975321	Enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS Strong transcription Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
3	nsv1010714	chr4:78742505-78991030	Weak transcription Genic enhancers Bivalent/Poised TSS Enhancers Strong transcription Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
4	nsv516836	chr4:78748977-78981919	Strong transcription Flanking Active TSS Weak transcription Active TSS Enhancers Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
5	nsv594704	chr4:78748977-78981919	Strong transcription Enhancers Weak transcription Bivalent/Poised TSS Genic enhancers Active TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
6	nsv461562	chr4:78757015-78981919	Enhancers Weak transcription Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
7	nsv461563	chr4:78757015-78981919	Strong transcription Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Enhancers Weak transcription Active TSS Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
8	nsv594705	chr4:78757015-78981919	Enhancers Genic enhancers Strong transcription Weak transcription Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
9	nsv1008217	chr4:78777531-78957311	Strong transcription Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
10	nsv537145	chr4:78777531-78957311	Active TSS Enhancers Strong transcription Weak transcription Genic enhancers ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
11	nsv534024	chr4:78785189-79437403	ZNF genes & repeats Flanking Active TSS Enhancers Active TSS Weak transcription Strong transcription Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	18 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs6854895	MRPL1	cis	multi-tissue	Pritchard

Chromatin state (count:103 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:78784800-78859800	Weak transcription	Esophagus	oesophagus
2	chr4:78785000-78874400	Weak transcription	Right Ventricle	heart
3	chr4:78802400-78858400	Weak transcription	Aorta	Aorta
4	chr4:78806000-78881000	Weak transcription	Brain Hippocampus Middle	brain
5	chr4:78806600-78875600	Weak transcription	Colonic Mucosa	Colon
6	chr4:78808800-78852400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
7	chr4:78809600-78865400	Weak transcription	HUES6 Cell Line	embryonic stem cell
8	chr4:78809600-78881200	Weak transcription	Rectal Smooth Muscle	rectum
9	chr4:78814600-78874400	Weak transcription	Pancreas	Pancrea
10	chr4:78816400-78866400	Weak transcription	Fetal Thymus	thymus
11	chr4:78816400-78876000	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
12	chr4:78816600-78875800	Weak transcription	Rectal Mucosa Donor 31	rectum
13	chr4:78818800-78872800	Weak transcription	Sigmoid Colon	Sigmoid Colon
14	chr4:78819200-78852000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
15	chr4:78821000-78866000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
16	chr4:78821400-78873200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
17	chr4:78830000-78866600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
18	chr4:78830200-78852000	Weak transcription	Stomach Smooth Muscle	stomach
19	chr4:78830400-78877000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
20	chr4:78831800-78865800	Weak transcription	Duodenum Mucosa	Duodenum
21	chr4:78832000-78858000	Weak transcription	Fetal Stomach	stomach
22	chr4:78833600-78865400	Weak transcription	Fetal Kidney	kidney
23	chr4:78834000-78852800	Weak transcription	HUES64 Cell Line	embryonic stem cell
24	chr4:78835400-78852600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
25	chr4:78842200-78865600	Weak transcription	H1 Cell Line	embryonic stem cell
26	chr4:78842400-78865400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
27	chr4:78843800-78852800	Weak transcription	Placenta	Placenta
28	chr4:78843800-78854200	Weak transcription	Gastric	stomach
29	chr4:78843800-78858000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
30	chr4:78843800-78858000	Weak transcription	Left Ventricle	heart
31	chr4:78843800-78865200	Weak transcription	Psoas Muscle	Psoas
32	chr4:78844000-78852400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
33	chr4:78844200-78871400	Weak transcription	NHDF-Ad	bronchial
34	chr4:78845200-78856000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
35	chr4:78847000-78852400	Weak transcription	Primary monocytes fromperipheralblood	blood
36	chr4:78847400-78852400	Weak transcription	Primary hematopoietic stem cells	blood
37	chr4:78847400-78853000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
38	chr4:78847400-78860200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
39	chr4:78847600-78852200	Weak transcription	Primary B cells from cord blood	blood
40	chr4:78847600-78852200	Weak transcription	Fetal Muscle Trunk	muscle
41	chr4:78847600-78852600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
42	chr4:78847600-78852800	Weak transcription	K562	blood
43	chr4:78847600-78865200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
44	chr4:78848000-78856400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
45	chr4:78848800-78869000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
46	chr4:78849400-78852000	Weak transcription	NHLF	lung
47	chr4:78849400-78853400	Enhancers	HUVEC	blood vessel
48	chr4:78849400-78876600	Weak transcription	Colon Smooth Muscle	Colon
49	chr4:78849600-78852000	Weak transcription	NH-A	brain
50	chr4:78849600-78871400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow

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