Variant report

Variant	rs334702
Chromosome Location	chr1:61618693-61618694
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr1:61599982..61604281-chr1:61617367..61621050,4	K562	blood:
2	chr1:61585280..61588265-chr1:61616173..61618887,3	K562	blood:
3	chr1:61605231..61608148-chr1:61617822..61620797,4	K562	blood:
4	chr1:61585280..61587671-chr1:61616173..61618887,2	K562	blood:
5	chr1:61519932..61522801-chr1:61616864..61618742,2	K562	blood:

Extended variants
information (count: 25 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:24)

rs_ID	r²[population]
rs168022	0.88[EUR][1000 genomes]
rs334698	0.98[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs334699	1.00[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs334700	1.00[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs334701	0.97[AFR][1000 genomes];0.88[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs334703	1.00[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs334704	1.00[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs334705	1.00[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs334706	0.98[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs334709	0.93[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs334712	0.90[EUR][1000 genomes]
rs334713	0.85[ASN][1000 genomes]
rs334724	0.90[EUR][1000 genomes]
rs334725	1.00[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs334726	1.00[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs334727	0.98[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs334728	0.97[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs334729	0.90[AFR][1000 genomes]
rs334732	0.87[EUR][1000 genomes]
rs382704	0.87[EUR][1000 genomes]
rs395936	0.82[ASN][1000 genomes]
rs4915728	0.87[EUR][1000 genomes]
rs694151	0.82[ASN][1000 genomes]
rs694161	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:72 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:61606000-61649000	Weak transcription	Spleen	Spleen
2	chr1:61607600-61622200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
3	chr1:61607800-61622600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
4	chr1:61609600-61622800	Weak transcription	Muscle Satellite Cultured Cells	--
5	chr1:61610000-61621800	Weak transcription	Fetal Brain Male	brain
6	chr1:61610000-61623400	Weak transcription	Fetal Brain Female	brain
7	chr1:61610200-61622200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
8	chr1:61610200-61623200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
9	chr1:61612000-61635800	Weak transcription	Lung	lung
10	chr1:61612800-61626200	Weak transcription	Fetal Muscle Trunk	muscle
11	chr1:61613400-61619800	Enhancers	Colon Smooth Muscle	Colon
12	chr1:61613800-61620600	Enhancers	Brain Hippocampus Middle	brain
13	chr1:61614800-61622000	Weak transcription	Ovary	ovary
14	chr1:61615000-61619000	Enhancers	Skeletal Muscle Male	skeletal muscle
15	chr1:61615200-61619600	Enhancers	Brain Anterior Caudate	brain
16	chr1:61615200-61620600	Enhancers	Brain Inferior Temporal Lobe	brain
17	chr1:61615200-61621000	Enhancers	Cortex derived primary cultured neurospheres	brain
18	chr1:61615400-61619600	Enhancers	Fetal Heart	heart
19	chr1:61615400-61620000	Enhancers	Brain Substantia Nigra	brain
20	chr1:61615400-61635000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
21	chr1:61615400-61635600	Weak transcription	Hela-S3	cervix
22	chr1:61615600-61620600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
23	chr1:61615600-61622600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
24	chr1:61615600-61622600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
25	chr1:61615800-61618800	Enhancers	Psoas Muscle	Psoas
26	chr1:61615800-61621600	Weak transcription	Right Ventricle	heart
27	chr1:61615800-61621800	Weak transcription	K562	blood
28	chr1:61615800-61622400	Weak transcription	NHEK	skin
29	chr1:61616000-61622000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
30	chr1:61616000-61628000	Weak transcription	Gastric	stomach
31	chr1:61616400-61619000	Enhancers	HepG2	liver
32	chr1:61616600-61618800	Enhancers	ES-I3 Cell Line	embryonic stem cell
33	chr1:61616600-61619600	Enhancers	Liver	Liver
34	chr1:61616800-61619400	Enhancers	Brain Cingulate Gyrus	brain
35	chr1:61616800-61622200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
36	chr1:61616800-61623200	Weak transcription	HUES6 Cell Line	embryonic stem cell
37	chr1:61617000-61619800	Enhancers	Rectal Smooth Muscle	rectum
38	chr1:61617000-61627800	Weak transcription	Esophagus	oesophagus
39	chr1:61617200-61618800	Enhancers	H9 Cell Line	embryonic stem cell
40	chr1:61617200-61618800	Enhancers	Right Atrium	heart
41	chr1:61617200-61618800	Enhancers	Skeletal Muscle Female	skeletal muscle
42	chr1:61617200-61619000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
43	chr1:61617200-61619200	Enhancers	Fetal Kidney	kidney
44	chr1:61617200-61619200	Enhancers	Sigmoid Colon	Sigmoid Colon
45	chr1:61617200-61619400	Enhancers	Brain Angular Gyrus	brain
46	chr1:61617200-61619600	Enhancers	Fetal Lung	lung
47	chr1:61617200-61619600	Enhancers	Small Intestine	intestine
48	chr1:61617200-61619800	Enhancers	Duodenum Smooth Muscle	Duodenum
49	chr1:61617200-61620000	Enhancers	Fetal Intestine Small	intestine
50	chr1:61617200-61620600	Enhancers	Fetal Stomach	stomach

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