Variant report

Variant	rs334705
Chromosome Location	chr1:61617072-61617073
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr1:61585280..61588265-chr1:61616173..61618887,3	K562	blood:
2	chr1:61585280..61587671-chr1:61616173..61618887,2	K562	blood:
3	chr1:61519932..61522801-chr1:61616864..61618742,2	K562	blood:

Extended variants
information (count: 41 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:40)

rs_ID	r²[population]
rs12064543	0.93[EUR][1000 genomes]
rs12070080	0.93[EUR][1000 genomes]
rs17121598	0.93[EUR][1000 genomes]
rs2807991	0.93[EUR][1000 genomes]
rs334698	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[YRI][hapmap];0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs334699	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs334700	1.00[CEU][hapmap];1.00[CHB][hapmap];0.89[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs334701	1.00[CHB][hapmap];0.97[AFR][1000 genomes]
rs334702	1.00[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs334703	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs334704	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs334706	1.00[CEU][hapmap];1.00[CHB][hapmap];0.89[YRI][hapmap];0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs334709	1.00[CEU][hapmap];1.00[CHB][hapmap];0.89[YRI][hapmap];0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs334710	1.00[CEU][hapmap];0.91[EUR][1000 genomes]
rs334713	1.00[CEU][hapmap];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs334716	1.00[CEU][hapmap];0.88[YRI][hapmap];0.82[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs334718	0.84[EUR][1000 genomes]
rs334719	0.86[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs334721	1.00[CEU][hapmap];0.90[EUR][1000 genomes]
rs334723	1.00[CEU][hapmap];0.88[YRI][hapmap];0.86[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs334725	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs334726	1.00[CEU][hapmap];1.00[CHB][hapmap];0.89[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs334727	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs334728	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[YRI][hapmap];0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs334729	1.00[CEU][hapmap];0.80[YRI][hapmap];0.90[AFR][1000 genomes];0.97[EUR][1000 genomes]
rs334730	1.00[CEU][hapmap];0.93[EUR][1000 genomes]
rs334731	1.00[CEU][hapmap];0.93[EUR][1000 genomes]
rs334733	1.00[CEU][hapmap];0.93[EUR][1000 genomes]
rs334734	1.00[CEU][hapmap];0.93[EUR][1000 genomes]
rs334737	0.93[EUR][1000 genomes]
rs334739	1.00[CEU][hapmap];0.93[EUR][1000 genomes]
rs3748543	1.00[CEU][hapmap];0.93[EUR][1000 genomes]
rs395936	1.00[CEU][hapmap];0.80[YRI][hapmap];0.93[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs406412	1.00[CEU][hapmap];0.80[YRI][hapmap];0.93[EUR][1000 genomes]
rs440611	0.93[EUR][1000 genomes]
rs4546954	0.93[EUR][1000 genomes]
rs4915586	0.93[EUR][1000 genomes]
rs6587912	1.00[CEU][hapmap];0.93[EUR][1000 genomes]
rs694151	1.00[CEU][hapmap];0.93[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs694161	1.00[CEU][hapmap];0.90[EUR][1000 genomes];0.82[ASN][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1008634	chr1:61613785-61671468	Enhancers Flanking Active TSS Weak transcription Active TSS Strong transcription Genic enhancers Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:71 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:61600000-61617200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
2	chr1:61605400-61617200	Weak transcription	H9 Cell Line	embryonic stem cell
3	chr1:61606000-61649000	Weak transcription	Spleen	Spleen
4	chr1:61607600-61617800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
5	chr1:61607600-61622200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
6	chr1:61607800-61617200	Weak transcription	Duodenum Smooth Muscle	Duodenum
7	chr1:61607800-61617800	Weak transcription	Rectal Mucosa Donor 29	rectum
8	chr1:61607800-61618000	Weak transcription	HUES64 Cell Line	embryonic stem cell
9	chr1:61607800-61622600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
10	chr1:61608400-61617200	Weak transcription	Fetal Stomach	stomach
11	chr1:61608600-61617800	Weak transcription	Adipose Nuclei	Adipose
12	chr1:61609200-61617200	Weak transcription	Sigmoid Colon	Sigmoid Colon
13	chr1:61609200-61617400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
14	chr1:61609600-61622800	Weak transcription	Muscle Satellite Cultured Cells	--
15	chr1:61610000-61621800	Weak transcription	Fetal Brain Male	brain
16	chr1:61610000-61623400	Weak transcription	Fetal Brain Female	brain
17	chr1:61610200-61617200	Weak transcription	Pancreas	Pancrea
18	chr1:61610200-61622200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
19	chr1:61610200-61623200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
20	chr1:61612000-61635800	Weak transcription	Lung	lung
21	chr1:61612400-61617200	Weak transcription	Fetal Muscle Leg	muscle
22	chr1:61612800-61626200	Weak transcription	Fetal Muscle Trunk	muscle
23	chr1:61613400-61619800	Enhancers	Colon Smooth Muscle	Colon
24	chr1:61613600-61617400	Enhancers	A549	lung
25	chr1:61613800-61620600	Enhancers	Brain Hippocampus Middle	brain
26	chr1:61614200-61617200	Weak transcription	Duodenum Mucosa	Duodenum
27	chr1:61614200-61617400	Weak transcription	Colonic Mucosa	Colon
28	chr1:61614400-61617400	Weak transcription	Rectal Mucosa Donor 31	rectum
29	chr1:61614600-61617200	Weak transcription	Fetal Intestine Small	intestine
30	chr1:61614800-61617200	Weak transcription	Left Ventricle	heart
31	chr1:61614800-61622000	Weak transcription	Ovary	ovary
32	chr1:61615000-61619000	Enhancers	Skeletal Muscle Male	skeletal muscle
33	chr1:61615200-61617400	Weak transcription	Stomach Smooth Muscle	stomach
34	chr1:61615200-61619600	Enhancers	Brain Anterior Caudate	brain
35	chr1:61615200-61620600	Enhancers	Brain Inferior Temporal Lobe	brain
36	chr1:61615200-61621000	Enhancers	Cortex derived primary cultured neurospheres	brain
37	chr1:61615400-61617200	Weak transcription	Fetal Intestine Large	intestine
38	chr1:61615400-61619600	Enhancers	Fetal Heart	heart
39	chr1:61615400-61620000	Enhancers	Brain Substantia Nigra	brain
40	chr1:61615400-61635000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
41	chr1:61615400-61635600	Weak transcription	Hela-S3	cervix
42	chr1:61615600-61617200	Weak transcription	Brain Angular Gyrus	brain
43	chr1:61615600-61617600	Weak transcription	Stomach Mucosa	stomach
44	chr1:61615600-61620600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
45	chr1:61615600-61622600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
46	chr1:61615600-61622600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
47	chr1:61615800-61618800	Enhancers	Psoas Muscle	Psoas
48	chr1:61615800-61621600	Weak transcription	Right Ventricle	heart
49	chr1:61615800-61621800	Weak transcription	K562	blood
50	chr1:61615800-61622400	Weak transcription	NHEK	skin

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