Variant report

Variant	rs17163347
Chromosome Location	chr1:222806668-222806669
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:0)
CpG islands
(count:0)
Chromatin interactive
region (count:10)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:10 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:222800786..222803486-chr1:222805322..222806827,2	K562	blood:
2	chr1:222637935..222640112-chr1:222806335..222808096,3	MCF-7	breast:
3	chr1:222788507..222790055-chr1:222805799..222808069,2	K562	blood:
4	chr1:222637300..222641837-chr1:222805384..222811783,8	MCF-7	breast:
5	chr1:222797326..222799070-chr1:222805165..222807968,2	K562	blood:
6	chr1:222790899..222794415-chr1:222804722..222806870,4	MCF-7	breast:
7	chr1:222791343..222795260-chr1:222806268..222810918,6	K562	blood:
8	chr1:222806292..222810839-chr1:222815256..222818233,6	MCF-7	breast:
9	chr1:222803771..222808064-chr1:222812270..222818354,12	K562	blood:
10	chr1:222637338..222639462-chr1:222805621..222807759,2	K562	blood:

No data

Variant related genes	Relation type
ENSG00000154305	Chromatin interaction
ENSG00000229399	Chromatin interaction
ENSG00000234419	Chromatin interaction

Extended variants
information (count: 20 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:16)

rs_ID	r²[population]
rs17011702	1.00[AMR][1000 genomes]
rs17163458	1.00[AMR][1000 genomes]
rs17163479	1.00[AMR][1000 genomes]
rs17163502	1.00[AMR][1000 genomes]
rs74145517	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74145518	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74145541	1.00[AMR][1000 genomes]
rs74145543	1.00[AMR][1000 genomes]
rs74145544	1.00[AMR][1000 genomes]
rs74145547	1.00[AMR][1000 genomes]
rs74145550	1.00[AMR][1000 genomes]
rs74145551	1.00[AMR][1000 genomes]
rs74145552	1.00[AMR][1000 genomes]
rs74145553	1.00[AMR][1000 genomes]
rs74145556	1.00[AMR][1000 genomes]
rs74145562	1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv999185	chr1:222500725-223278032	Strong transcription Enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	45 gene(s)	inside rSNPs	diseases
2	nsv535304	chr1:222500725-223278032	Enhancers Flanking Active TSS Weak transcription Active TSS Genic enhancers Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	45 gene(s)	inside rSNPs	diseases
3	nsv873205	chr1:222718718-222923351	Weak transcription Strong transcription Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Enhancers Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	34 gene(s)	inside rSNPs	diseases
4	nsv1012537	chr1:222755091-223512243	Weak transcription Strong transcription Enhancers Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	48 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:126 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:222792400-222816600	Weak transcription	Small Intestine	intestine
2	chr1:222792600-222816600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
3	chr1:222792600-222817000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr1:222793200-222816600	Weak transcription	Primary neutrophils fromperipheralblood	blood
5	chr1:222793200-222816600	Weak transcription	Hela-S3	cervix
6	chr1:222793600-222816600	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
7	chr1:222794000-222806800	Strong transcription	Primary T cells from cord blood	blood
8	chr1:222794600-222807200	Strong transcription	Fetal Thymus	thymus
9	chr1:222794600-222809800	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
10	chr1:222794600-222810400	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
11	chr1:222794600-222810400	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
12	chr1:222794600-222813400	Strong transcription	iPS-20b Cell Line	embryonic stem cell
13	chr1:222794600-222813600	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
14	chr1:222794600-222814000	Strong transcription	HUES64 Cell Line	embryonic stem cell
15	chr1:222794600-222815000	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
16	chr1:222794800-222813200	Strong transcription	HUES48 Cell Line	embryonic stem cell
17	chr1:222794800-222813600	Strong transcription	Monocytes-CD14+_RO01746	blood
18	chr1:222795200-222807000	Strong transcription	HepG2	liver
19	chr1:222795200-222807600	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
20	chr1:222795200-222807600	Strong transcription	Fetal Muscle Trunk	muscle
21	chr1:222795200-222807800	Strong transcription	Sigmoid Colon	Sigmoid Colon
22	chr1:222795400-222806800	Strong transcription	Stomach Smooth Muscle	stomach
23	chr1:222795400-222807200	Strong transcription	Primary T cells fromperipheralblood	blood
24	chr1:222795400-222807600	Strong transcription	Primary T helper cells PMA-I stimulated	--
25	chr1:222795400-222810400	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
26	chr1:222795400-222810600	Strong transcription	iPS-18 Cell Line	embryonic stem cell
27	chr1:222795400-222810600	Strong transcription	Fetal Muscle Leg	muscle
28	chr1:222795400-222812000	Strong transcription	Rectal Mucosa Donor 29	rectum
29	chr1:222795400-222813400	Strong transcription	HUES6 Cell Line	embryonic stem cell
30	chr1:222795600-222807200	Strong transcription	H1 Cell Line	embryonic stem cell
31	chr1:222795600-222807200	Strong transcription	Primary T helper cells fromperipheralblood	blood
32	chr1:222795600-222810600	Strong transcription	Cortex derived primary cultured neurospheres	brain
33	chr1:222795800-222810600	Strong transcription	Adipose Nuclei	Adipose
34	chr1:222796000-222807600	Strong transcription	Skeletal Muscle Female	skeletal muscle
35	chr1:222796200-222807800	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
36	chr1:222797000-222809200	Strong transcription	Fetal Intestine Large	intestine
37	chr1:222797000-222812400	Strong transcription	Rectal Mucosa Donor 31	rectum
38	chr1:222797400-222807000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
39	chr1:222797400-222807000	Strong transcription	Skeletal Muscle Male	skeletal muscle
40	chr1:222797400-222810600	Strong transcription	Duodenum Mucosa	Duodenum
41	chr1:222797600-222810600	Strong transcription	Placenta	Placenta
42	chr1:222797800-222807000	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
43	chr1:222798200-222807600	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
44	chr1:222798400-222807200	Strong transcription	Ovary	ovary
45	chr1:222798400-222812000	Strong transcription	Fetal Stomach	stomach
46	chr1:222798800-222808200	Strong transcription	Brain Hippocampus Middle	brain
47	chr1:222799000-222807200	Strong transcription	Fetal Brain Female	brain
48	chr1:222799000-222807600	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
49	chr1:222799000-222807600	Strong transcription	Left Ventricle	heart
50	chr1:222799200-222807000	Strong transcription	Dnd41	blood

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