Variant report

Variant	rs4329313
Chromosome Location	chr8:131012991-131012992
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr8:131008248..131015000-chr8:131026148..131029127,9	K562	blood:
2	chr8:131011363..131013823-chr8:131017566..131020563,3	MCF-7	breast:
3	chr8:131010470..131015100-chr8:131019285..131023448,5	K562	blood:
4	chr8:131007021..131009238-chr8:131011453..131013766,3	MCF-7	breast:

Variant related genes	Relation type
ENSG00000153310	Chromatin interaction
ENSG00000264653	Chromatin interaction

Extended variants
information (count: 28 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:19)

rs_ID	r²[population]
rs10110808	0.98[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12541347	0.98[ASN][1000 genomes]
rs12547810	0.95[ASN][1000 genomes]
rs12548639	0.98[ASN][1000 genomes]
rs12548670	0.81[AFR][1000 genomes];0.85[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs12550248	0.90[ASN][1000 genomes]
rs1563167	0.80[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1971905	0.87[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1976582	0.97[ASN][1000 genomes]
rs35830950	0.88[ASN][1000 genomes]
rs4733757	0.97[ASN][1000 genomes]
rs6470789	0.97[ASN][1000 genomes]
rs7003672	0.92[ASN][1000 genomes]
rs7016267	0.87[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7016345	0.98[ASN][1000 genomes]
rs7388128	0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs749029	0.81[ASN][1000 genomes]
rs874579	0.81[ASN][1000 genomes]
rs882446	0.81[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	nsv1018045	chr8:130863644-131122644	Flanking Active TSS Enhancers Weak transcription Strong transcription Genic enhancers Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	13 gene(s)	inside rSNPs	diseases
2	nsv612231	chr8:130868212-131132592	Enhancers Weak transcription Strong transcription Flanking Active TSS Genic enhancers Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	13 gene(s)	inside rSNPs	diseases
3	nsv524349	chr8:130868363-131132592	Enhancers Weak transcription Bivalent Enhancer Genic enhancers Flanking Active TSS Strong transcription Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	13 gene(s)	inside rSNPs	diseases
4	nsv1021229	chr8:130887132-131057897	Weak transcription Enhancers Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Strong transcription Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	9 gene(s)	inside rSNPs	diseases
5	nsv1017292	chr8:130887132-131107258	Strong transcription Enhancers Flanking Active TSS Weak transcription Genic enhancers Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	12 gene(s)	inside rSNPs	diseases
6	nsv465808	chr8:130963259-131118658	Strong transcription Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
7	nsv612232	chr8:130963259-131118658	Genic enhancers Enhancers Strong transcription Weak transcription Flanking Active TSS Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
8	nsv465809	chr8:131005345-131031827	ZNF genes & repeats Weak transcription Flanking Bivalent TSS/Enh Strong transcription Enhancers Genic enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	5 gene(s)	inside rSNPs	diseases
9	nsv612233	chr8:131005345-131031827	Enhancers Weak transcription Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	5 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:99 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:130996600-131017400	Weak transcription	Fetal Intestine Small	intestine
2	chr8:130998400-131017400	Weak transcription	Fetal Intestine Large	intestine
3	chr8:131004600-131013400	Enhancers	Primary T helper cells fromperipheralblood	blood
4	chr8:131005800-131013600	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
5	chr8:131006000-131016200	Genic enhancers	Primary B cells from peripheral blood	blood
6	chr8:131006200-131013800	Enhancers	HMEC	breast
7	chr8:131006400-131013000	Enhancers	Primary hematopoietic stem cells short term culture	blood
8	chr8:131006400-131013600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
9	chr8:131007200-131013000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
10	chr8:131007800-131014800	Enhancers	Primary T helper naive cells from peripheral blood	blood
11	chr8:131008200-131015600	Weak transcription	Sigmoid Colon	Sigmoid Colon
12	chr8:131008400-131013600	Enhancers	Primary T killer memory cells from peripheral blood	blood
13	chr8:131008400-131020600	Weak transcription	Psoas Muscle	Psoas
14	chr8:131008800-131015600	Weak transcription	Pancreas	Pancrea
15	chr8:131009000-131013200	Weak transcription	Thymus	Thymus
16	chr8:131009000-131013400	Enhancers	NHEK	skin
17	chr8:131009000-131021800	Weak transcription	Colonic Mucosa	Colon
18	chr8:131009400-131026200	Genic enhancers	Primary Natural Killer cells fromperipheralblood	blood
19	chr8:131010000-131017400	Weak transcription	Rectal Mucosa Donor 29	rectum
20	chr8:131010000-131020200	Weak transcription	Skeletal Muscle Male	skeletal muscle
21	chr8:131010000-131026800	Weak transcription	Duodenum Smooth Muscle	Duodenum
22	chr8:131010000-131027000	Weak transcription	Rectal Smooth Muscle	rectum
23	chr8:131010000-131027000	Weak transcription	Small Intestine	intestine
24	chr8:131010200-131022600	Weak transcription	Duodenum Mucosa	Duodenum
25	chr8:131010400-131020000	Weak transcription	Rectal Mucosa Donor 31	rectum
26	chr8:131010600-131015200	Weak transcription	Fetal Stomach	stomach
27	chr8:131010600-131020600	Weak transcription	Stomach Smooth Muscle	stomach
28	chr8:131010800-131014200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
29	chr8:131010800-131016400	Weak transcription	H9 Cell Line	embryonic stem cell
30	chr8:131010800-131020400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
31	chr8:131011000-131027600	Weak transcription	Stomach Mucosa	stomach
32	chr8:131011400-131013600	Weak transcription	Primary T cells from cord blood	blood
33	chr8:131011400-131015200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
34	chr8:131011400-131016000	Genic enhancers	Monocytes-CD14+_RO01746	blood
35	chr8:131011400-131018400	Genic enhancers	Primary T cells fromperipheralblood	blood
36	chr8:131011600-131013200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
37	chr8:131011600-131013800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
38	chr8:131011600-131015800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
39	chr8:131011600-131026800	Weak transcription	Brain Germinal Matrix	brain
40	chr8:131011800-131019800	Weak transcription	Fetal Muscle Leg	muscle
41	chr8:131011800-131020800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
42	chr8:131012000-131013600	Enhancers	GM12878-XiMat	blood
43	chr8:131012000-131017400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
44	chr8:131012000-131017600	Weak transcription	Right Ventricle	heart
45	chr8:131012000-131017800	Weak transcription	Fetal Muscle Trunk	muscle
46	chr8:131012000-131019400	Weak transcription	Brain Hippocampus Middle	brain
47	chr8:131012200-131013400	Strong transcription	Primary B cells from cord blood	blood
48	chr8:131012200-131013800	Genic enhancers	Primary T helper 17 cells PMA-I stimulated	--
49	chr8:131012200-131014400	Weak transcription	Fetal Thymus	thymus
50	chr8:131012200-131017400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived

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