Variant report

Variant	rs7434721
Chromosome Location	chr4:48516970-48516971
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr4:48510100..48513571-chr4:48516214..48518861,3	K562	blood:

Extended variants
information (count: 76 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:71)

rs_ID	r²[population]
rs10034207	1.00[AMR][1000 genomes]
rs10049760	1.00[YRI][hapmap];1.00[AMR][1000 genomes]
rs10755182	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10805171	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10805172	0.82[YRI][hapmap];1.00[AMR][1000 genomes]
rs10938535	1.00[AMR][1000 genomes]
rs10938538	1.00[AMR][1000 genomes]
rs10938539	1.00[AMR][1000 genomes]
rs10938541	1.00[AMR][1000 genomes]
rs12500224	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12500244	1.00[AMR][1000 genomes]
rs12507546	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs13125379	1.00[AMR][1000 genomes]
rs1474072	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs1517673	1.00[AMR][1000 genomes]
rs1517676	1.00[AMR][1000 genomes]
rs1517677	1.00[AMR][1000 genomes]
rs1533511	1.00[AMR][1000 genomes]
rs1554257	1.00[AMR][1000 genomes]
rs1616561	1.00[AMR][1000 genomes]
rs1702796	1.00[AMR][1000 genomes]
rs1702799	1.00[YRI][hapmap];0.82[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs1712762	1.00[YRI][hapmap]
rs1712771	1.00[AMR][1000 genomes]
rs1949422	1.00[AMR][1000 genomes]
rs2138866	1.00[YRI][hapmap];1.00[AMR][1000 genomes]
rs2138867	1.00[AMR][1000 genomes]
rs28371079	1.00[AMR][1000 genomes]
rs2883410	1.00[AMR][1000 genomes]
rs2940319	1.00[YRI][hapmap];1.00[AMR][1000 genomes]
rs4235155	0.82[YRI][hapmap];1.00[AMR][1000 genomes]
rs4235157	1.00[AMR][1000 genomes]
rs4235159	0.82[AFR][1000 genomes]
rs4330326	1.00[AMR][1000 genomes]
rs4558842	1.00[AMR][1000 genomes]
rs4694896	1.00[AMR][1000 genomes]
rs4694898	1.00[YRI][hapmap];0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs4694903	1.00[AMR][1000 genomes]
rs4695385	1.00[AMR][1000 genomes]
rs4695386	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs4695390	1.00[YRI][hapmap];0.86[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs4998005	1.00[AMR][1000 genomes]
rs6447642	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6447643	1.00[YRI][hapmap]
rs6447654	1.00[AMR][1000 genomes]
rs6447656	1.00[AMR][1000 genomes]
rs6447657	1.00[AMR][1000 genomes]
rs6821456	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6823351	1.00[AMR][1000 genomes]
rs6827481	1.00[AMR][1000 genomes]
rs6828500	1.00[AMR][1000 genomes]
rs6835757	1.00[YRI][hapmap];0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6846797	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6848222	1.00[AMR][1000 genomes]
rs6848417	1.00[AMR][1000 genomes]
rs6849798	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6853876	0.83[YRI][hapmap];1.00[AMR][1000 genomes]
rs707720	1.00[AMR][1000 genomes]
rs7664507	1.00[AMR][1000 genomes]
rs7689293	0.82[YRI][hapmap];1.00[AMR][1000 genomes]
rs7689662	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7692480	1.00[AMR][1000 genomes]
rs776581	1.00[YRI][hapmap];1.00[AMR][1000 genomes]
rs776583	1.00[YRI][hapmap];0.82[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs776587	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs776589	1.00[AMR][1000 genomes]
rs776595	0.82[YRI][hapmap];0.82[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs776603	1.00[AMR][1000 genomes]
rs938791	1.00[AMR][1000 genomes]
rs9997932	1.00[AMR][1000 genomes]
rs9998178	1.00[AMR][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	nsv470034	chr4:48427773-48605628	Strong transcription Weak transcription Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS Flanking Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	7 gene(s)	inside rSNPs	diseases
2	nsv594121	chr4:48427773-48605628	Bivalent/Poised TSS Weak transcription Strong transcription Flanking Active TSS Enhancers Genic enhancers Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	7 gene(s)	inside rSNPs	diseases
3	nsv829925	chr4:48467693-48639342	Weak transcription Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Active TSS Bivalent Enhancer Enhancers Bivalent/Poised TSS ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
4	nsv1002674	chr4:48507608-49032909	Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Strong transcription Enhancers ZNF genes & repeats Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
5	nsv537087	chr4:48507608-49032909	Flanking Active TSS Weak transcription Strong transcription Active TSS Enhancers Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:125 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:48493600-48523000	Weak transcription	Right Ventricle	heart
2	chr4:48495400-48523000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr4:48496200-48540600	Weak transcription	Pancreatic Islets	Pancreatic Islet
4	chr4:48497000-48521600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
5	chr4:48498200-48539600	Strong transcription	Rectal Mucosa Donor 29	rectum
6	chr4:48498200-48540000	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr4:48498600-48593000	Strong transcription	Rectal Mucosa Donor 31	rectum
8	chr4:48499000-48578800	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
9	chr4:48499000-48589400	Strong transcription	Primary monocytes fromperipheralblood	blood
10	chr4:48499200-48540000	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
11	chr4:48499400-48527400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
12	chr4:48499600-48581400	Strong transcription	Dnd41	blood
13	chr4:48499800-48540000	Strong transcription	Primary T cells fromperipheralblood	blood
14	chr4:48500200-48517400	Strong transcription	Primary B cells from peripheral blood	blood
15	chr4:48500200-48588800	Strong transcription	Monocytes-CD14+_RO01746	blood
16	chr4:48500400-48540000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
17	chr4:48501000-48538800	Strong transcription	Primary neutrophils fromperipheralblood	blood
18	chr4:48501400-48578600	Strong transcription	Primary T helper cells fromperipheralblood	blood
19	chr4:48501600-48523000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
20	chr4:48503400-48520400	Weak transcription	NHLF	lung
21	chr4:48504400-48575400	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
22	chr4:48504600-48534400	Strong transcription	Liver	Liver
23	chr4:48505200-48575400	Strong transcription	Primary T helper cells PMA-I stimulated	--
24	chr4:48505400-48538600	Strong transcription	HUES64 Cell Line	embryonic stem cell
25	chr4:48505400-48540000	Strong transcription	HSMM	muscle
26	chr4:48505600-48517200	Strong transcription	Breast Myoepithelial Primary Cells	Breast
27	chr4:48506000-48538800	Strong transcription	Duodenum Mucosa	Duodenum
28	chr4:48506400-48517200	Strong transcription	iPS-20b Cell Line	embryonic stem cell
29	chr4:48506400-48518400	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
30	chr4:48506800-48517600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
31	chr4:48507000-48517200	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
32	chr4:48507200-48517400	Strong transcription	HUES48 Cell Line	embryonic stem cell
33	chr4:48507200-48517400	Strong transcription	Fetal Intestine Large	intestine
34	chr4:48507200-48564000	Strong transcription	Fetal Thymus	thymus
35	chr4:48507400-48517200	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
36	chr4:48507400-48517400	Strong transcription	GM12878-XiMat	blood
37	chr4:48507400-48536200	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
38	chr4:48507600-48517200	Strong transcription	Primary hematopoietic stem cells short term culture	blood
39	chr4:48507600-48517200	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
40	chr4:48507600-48517200	Strong transcription	NHEK	skin
41	chr4:48507600-48517400	Strong transcription	HUVEC	blood vessel
42	chr4:48507600-48517600	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
43	chr4:48507600-48517600	Strong transcription	Duodenum Smooth Muscle	Duodenum
44	chr4:48507600-48517600	Strong transcription	Skeletal Muscle Female	skeletal muscle
45	chr4:48507600-48519200	Strong transcription	Stomach Smooth Muscle	stomach
46	chr4:48507600-48568600	Strong transcription	Primary T cells from cord blood	blood
47	chr4:48507800-48517200	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--
48	chr4:48507800-48539400	Strong transcription	Primary B cells from cord blood	blood
49	chr4:48508800-48517200	Strong transcription	Muscle Satellite Cultured Cells	--
50	chr4:48508800-48538800	Strong transcription	Primary hematopoietic stem cells	blood

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