Variant report

Variant	rs34965128
Chromosome Location	chr11:5704899-5704900
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	SP1	chr11:5704741-5705257	GM12878	blood:	n/a	n/a
2	POLR2A	chr11:5703536-5706824	IMR90	lung:	n/a	n/a
3	NFYB	chr11:5704740-5705165	Hela-S3	cervix:	n/a	chr11:5705025-5705040
4	POLR2A	chr11:5704569-5705462	GM12892	blood:	n/a	n/a
5	POLR2A	chr11:5704860-5705346	GM12891	blood:	n/a	n/a
6	POLR2A	chr11:5704791-5706700	GM12878	blood:	n/a	n/a
7	NFYB	chr11:5704605-5705595	GM12878	blood:	n/a	chr11:5705025-5705040
8	POLR2A	chr11:5704892-5705298	HUVEC	blood vessel:	n/a	n/a
9	SP1	chr11:5704591-5705025	HepG2	liver:	n/a	n/a
10	POU2F2	chr11:5704872-5706595	GM12878	blood:	n/a	n/a
11	SP1	chr11:5704588-5705249	GM12878	blood:	n/a	n/a
12	POLR2A	chr11:5704753-5706635	GM12878	blood:	n/a	n/a
13	NFYB	chr11:5704616-5705210	K562	blood:	n/a	chr11:5705025-5705040
14	POLR2A	chr11:5704793-5705403	GM12892	blood:	n/a	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr11:5523660..5528079-chr11:5704615..5707879,4	K562	blood:
2	chr11:5700658..5702927-chr11:5704276..5706133,2	K562	blood:
3	11:5033143-5038367..11:5700314-5707362	K562	blood:
4	11:4801044-4820112..11:5700314-5707362	H1-hESC	embryonic stem cell:	embryo
5	11:4988858-5002113..11:5700314-5707362	Hela-S3	cervix:
6	chr11:5524818..5527723-chr11:5704615..5707499,2	K562	blood:

Variant related genes	Relation type
TRIM5	TF binding region
ENSG00000213931	Chromatin interaction
ENSG00000196565	Chromatin interaction
ENSG00000231070	Chromatin interaction
ENSG00000167355	Chromatin interaction
ENSG00000132256	Chromatin interaction
ENSG00000225003	Chromatin interaction
ENSG00000176951	Chromatin interaction
ENSG00000224300	Chromatin interaction

Extended variants
information (count: 45 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:35)

rs_ID	r²[population]
rs10461515	0.87[AFR][1000 genomes];0.88[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs10512892	0.91[ASN][1000 genomes]
rs13159894	0.80[AFR][1000 genomes];0.83[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs13167360	0.93[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs13180931	0.97[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs13182174	0.82[AFR][1000 genomes];0.84[AMR][1000 genomes];0.80[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs13187179	0.80[AFR][1000 genomes];0.83[EUR][1000 genomes]
rs13188257	0.87[AFR][1000 genomes];0.88[AMR][1000 genomes];0.92[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs13189219	0.81[EUR][1000 genomes]
rs16879113	0.93[AFR][1000 genomes];0.93[AMR][1000 genomes];0.94[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2137133	0.97[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs34229766	0.93[AFR][1000 genomes];0.93[AMR][1000 genomes];0.95[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs34243952	0.81[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs34293593	0.81[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs34596323	0.87[AFR][1000 genomes];0.93[AMR][1000 genomes];0.94[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs34629161	0.82[EUR][1000 genomes]
rs34730675	0.93[AFR][1000 genomes];0.88[AMR][1000 genomes];0.89[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs34832270	0.93[AMR][1000 genomes];0.94[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs34902459	0.80[AFR][1000 genomes];0.83[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs34906853	0.87[AFR][1000 genomes];0.88[AMR][1000 genomes];0.89[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs34992228	0.83[EUR][1000 genomes]
rs35066865	0.97[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs35174411	1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];0.95[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs35371759	0.83[EUR][1000 genomes]
rs35700380	0.93[AMR][1000 genomes];0.94[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs36047540	0.93[AFR][1000 genomes];0.93[AMR][1000 genomes];0.96[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs36184257	0.84[AFR][1000 genomes];0.80[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs4030575	1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62365933	0.81[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs62386168	0.97[AFR][1000 genomes];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs62386223	0.93[AFR][1000 genomes];0.98[AMR][1000 genomes];0.94[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs62387343	0.87[AFR][1000 genomes];0.84[AMR][1000 genomes];0.94[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs62387346	0.81[AFR][1000 genomes];0.93[AMR][1000 genomes];0.94[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs62387347	0.87[AFR][1000 genomes];0.93[AMR][1000 genomes];0.94[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs71631462	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:10 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1046068	chr11:5335943-6063742	Strong transcription Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS Enhancers Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	89 gene(s)	inside rSNPs	diseases
2	nsv896939	chr11:5497799-5809548	Enhancers Active TSS Weak transcription Strong transcription Flanking Active TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	48 gene(s)	inside rSNPs	diseases
3	nsv553241	chr11:5506034-6203685	Genic enhancers Strong transcription Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	74 gene(s)	inside rSNPs	diseases
4	nsv1041568	chr11:5585716-5765688	Strong transcription Enhancers Weak transcription Active TSS Genic enhancers Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh 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
5	nsv1053414	chr11:5612989-6030212	Flanking Active TSS Active TSS Enhancers Bivalent/Poised TSS Strong transcription Weak transcription Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	50 gene(s)	inside rSNPs	diseases
6	nsv530216	chr11:5614439-6468232	Transcr. at gene 5' and 3' Flanking Active TSS Active TSS Enhancers Bivalent Enhancer Weak transcription Strong transcription Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	90 gene(s)	inside rSNPs	diseases
7	nsv553273	chr11:5639873-5871831	Strong transcription Weak transcription Active TSS Flanking Active TSS Enhancers Genic enhancers Bivalent Enhancer ZNF genes & repeats 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	37 gene(s)	inside rSNPs	diseases
8	nsv1036389	chr11:5695451-6177680	Weak transcription Bivalent Enhancer Genic enhancers Flanking Active TSS Active TSS Enhancers Bivalent/Poised TSS Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	55 gene(s)	inside rSNPs	diseases
9	nsv540943	chr11:5695451-6177680	Strong transcription Flanking Active TSS Enhancers Weak transcription Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	55 gene(s)	inside rSNPs	diseases
10	nsv896948	chr11:5701281-5719667	Weak transcription Enhancers Active TSS Flanking Active TSS Strong transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:5674800-5705400	Weak transcription	Psoas Muscle	Psoas
2	chr11:5684000-5705400	Weak transcription	Brain Substantia Nigra	brain
3	chr11:5684200-5705400	Weak transcription	Skeletal Muscle Male	skeletal muscle
4	chr11:5685400-5705400	Weak transcription	Stomach Mucosa	stomach
5	chr11:5688000-5705600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
6	chr11:5691000-5705000	Weak transcription	Hela-S3	cervix
7	chr11:5691000-5705400	Weak transcription	Fetal Brain Male	brain
8	chr11:5694200-5705400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
9	chr11:5696000-5705200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
10	chr11:5697000-5705600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
11	chr11:5698200-5705400	Weak transcription	Brain Cingulate Gyrus	brain
12	chr11:5700000-5705200	Weak transcription	Skeletal Muscle Female	skeletal muscle
13	chr11:5700200-5705400	Weak transcription	Brain Anterior Caudate	brain
14	chr11:5700200-5705400	Weak transcription	HepG2	liver
15	chr11:5700400-5705200	Weak transcription	Fetal Kidney	kidney
16	chr11:5700400-5705200	Weak transcription	K562	blood
17	chr11:5700400-5705400	Weak transcription	Brain Hippocampus Middle	brain
18	chr11:5700600-5705400	Weak transcription	HUES48 Cell Line	embryonic stem cell
19	chr11:5700600-5705400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
20	chr11:5700600-5705600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
21	chr11:5700800-5705200	Weak transcription	Small Intestine	intestine
22	chr11:5701000-5705400	Weak transcription	NHDF-Ad	bronchial
23	chr11:5701200-5705200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
24	chr11:5701200-5705200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
25	chr11:5701200-5705400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
26	chr11:5701400-5705000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
27	chr11:5701400-5705000	Weak transcription	Primary neutrophils fromperipheralblood	blood
28	chr11:5701400-5705000	Weak transcription	Cortex derived primary cultured neurospheres	brain
29	chr11:5701400-5705000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
30	chr11:5701400-5705000	Weak transcription	Rectal Smooth Muscle	rectum
31	chr11:5701400-5705000	Weak transcription	Thymus	Thymus
32	chr11:5701400-5705200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
33	chr11:5701400-5705200	Weak transcription	Muscle Satellite Cultured Cells	--
34	chr11:5701400-5705200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
35	chr11:5701400-5705200	Weak transcription	Adipose Nuclei	Adipose
36	chr11:5701400-5705200	Weak transcription	Fetal Muscle Trunk	muscle
37	chr11:5701400-5705200	Weak transcription	Right Ventricle	heart
38	chr11:5701400-5705200	Weak transcription	A549	lung
39	chr11:5701400-5705200	Weak transcription	NHEK	skin
40	chr11:5701400-5705200	Weak transcription	Osteobl	bone
41	chr11:5701400-5705400	Weak transcription	H9 Cell Line	embryonic stem cell
42	chr11:5701400-5705400	Weak transcription	HUES6 Cell Line	embryonic stem cell
43	chr11:5701400-5705400	Weak transcription	HUES64 Cell Line	embryonic stem cell
44	chr11:5701400-5705400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
45	chr11:5701400-5705400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
46	chr11:5701400-5705400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
47	chr11:5701400-5705400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
48	chr11:5701400-5705400	Weak transcription	Ovary	ovary
49	chr11:5701400-5705400	Weak transcription	Sigmoid Colon	Sigmoid Colon
50	chr11:5701400-5705400	Weak transcription	HMEC	breast

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