Variant report

Variant	rs16926444
Chromosome Location	chr8:61648825-61648826
allele	C/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:8)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:8 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr8:61642321..61644074-chr8:61646813..61649325,2	MCF-7	breast:
2	chr8:61646629..61649455-chr8:61665377..61667682,2	K562	blood:
3	chr8:61647965..61650126-chr8:61662487..61664043,2	K562	blood:
4	chr8:61625249..61627166-chr8:61648012..61650874,2	MCF-7	breast:
5	chr8:61639286..61642173-chr8:61648208..61649850,2	K562	blood:
6	chr8:61646233..61649362-chr8:61650520..61653582,3	K562	blood:
7	chr8:61590474..61593758-chr8:61647007..61650642,4	MCF-7	breast:
8	chr8:61640669..61642679-chr8:61647528..61649316,2	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000171316	Chromatin interaction

Extended variants
information (count: 42 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:36)

rs_ID	r²[population]
rs10098584	1.00[ASN][1000 genomes]
rs10101023	1.00[ASN][1000 genomes]
rs13261519	1.00[ASN][1000 genomes]
rs13269361	1.00[ASN][1000 genomes]
rs13438807	1.00[ASN][1000 genomes]
rs16926379	1.00[ASN][1000 genomes]
rs16926398	1.00[ASN][1000 genomes]
rs16926440	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16926456	1.00[ASN][1000 genomes]
rs16926528	1.00[ASN][1000 genomes]
rs28539174	1.00[ASN][1000 genomes]
rs28539276	1.00[ASN][1000 genomes]
rs28667506	1.00[ASN][1000 genomes]
rs34833917	1.00[ASN][1000 genomes]
rs35777815	1.00[ASN][1000 genomes]
rs41272442	1.00[ASN][1000 genomes]
rs62524908	0.86[EUR][1000 genomes]
rs62524913	0.86[EUR][1000 genomes]
rs62524942	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62524943	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62524944	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62524946	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62524949	0.86[EUR][1000 genomes]
rs62524950	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62524951	1.00[AFR][1000 genomes];0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62524952	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs62524954	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62524956	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs62524957	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs62526484	0.86[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs62526485	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs62526486	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs62526528	1.00[ASN][1000 genomes]
rs6471895	1.00[ASN][1000 genomes]
rs7013969	1.00[ASN][1000 genomes]
rs730084	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:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv917756	chr8:60942299-61862796	Enhancers Weak transcription Active TSS Genic enhancers Bivalent/Poised TSS Strong transcription Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	74 gene(s)	inside rSNPs	diseases
2	nsv831335	chr8:61497540-61688992	Weak transcription Strong transcription Flanking Active TSS Enhancers Bivalent Enhancer Active TSS Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	33 gene(s)	inside rSNPs	diseases
3	nsv890945	chr8:61522008-61707725	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	33 gene(s)	inside rSNPs	diseases
4	nsv526196	chr8:61593569-61877623	Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	11 gene(s)	inside rSNPs	diseases
5	nsv1022801	chr8:61623974-61738067	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
6	nsv539632	chr8:61623974-61738067	Weak transcription Enhancers Strong transcription Active TSS ZNF genes & repeats Genic enhancers Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:91 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:61635000-61654200	Weak transcription	Fetal Intestine Small	intestine
2	chr8:61637000-61651200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr8:61637000-61654600	Weak transcription	Hela-S3	cervix
4	chr8:61638600-61651200	Weak transcription	Right Ventricle	heart
5	chr8:61638600-61654000	Weak transcription	NHEK	skin
6	chr8:61638600-61664200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
7	chr8:61642400-61649400	Enhancers	Primary neutrophils fromperipheralblood	blood
8	chr8:61644200-61659200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
9	chr8:61644800-61650800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
10	chr8:61644800-61659400	Weak transcription	Primary T helper cells fromperipheralblood	blood
11	chr8:61645000-61651200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
12	chr8:61645000-61651600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
13	chr8:61645000-61651800	Weak transcription	Fetal Brain Female	brain
14	chr8:61645000-61654200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
15	chr8:61645000-61654200	Weak transcription	Colonic Mucosa	Colon
16	chr8:61645200-61651200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
17	chr8:61645200-61651200	Weak transcription	Brain Cingulate Gyrus	brain
18	chr8:61645200-61651200	Weak transcription	Fetal Lung	lung
19	chr8:61645200-61651200	Weak transcription	Fetal Muscle Trunk	muscle
20	chr8:61645200-61651200	Weak transcription	Lung	lung
21	chr8:61645200-61651400	Weak transcription	Fetal Kidney	kidney
22	chr8:61645200-61651400	Weak transcription	Pancreas	Pancrea
23	chr8:61645200-61654200	Weak transcription	Fetal Intestine Large	intestine
24	chr8:61645400-61649400	Enhancers	Primary T helper cells PMA-I stimulated	--
25	chr8:61645400-61655000	Weak transcription	A549	lung
26	chr8:61645800-61649200	Enhancers	Brain Hippocampus Middle	brain
27	chr8:61646200-61651400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
28	chr8:61646200-61652200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
29	chr8:61646200-61656400	Weak transcription	Liver	Liver
30	chr8:61646400-61651200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
31	chr8:61646400-61654400	Weak transcription	Stomach Smooth Muscle	stomach
32	chr8:61646600-61649200	Enhancers	Primary B cells from peripheral blood	blood
33	chr8:61646600-61651200	Weak transcription	Brain Germinal Matrix	brain
34	chr8:61647000-61649200	Enhancers	H9 Cell Line	embryonic stem cell
35	chr8:61647000-61653600	Weak transcription	Fetal Brain Male	brain
36	chr8:61647200-61651400	Weak transcription	Right Atrium	heart
37	chr8:61647400-61651400	Weak transcription	Skeletal Muscle Female	skeletal muscle
38	chr8:61647400-61655200	Weak transcription	HepG2	liver
39	chr8:61647600-61649000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
40	chr8:61647600-61649200	Enhancers	Brain Substantia Nigra	brain
41	chr8:61648200-61649000	Enhancers	Sigmoid Colon	Sigmoid Colon
42	chr8:61648200-61649200	Enhancers	Cortex derived primary cultured neurospheres	brain
43	chr8:61648200-61649400	Enhancers	K562	blood
44	chr8:61648400-61649000	Enhancers	Primary hematopoietic stem cells short term culture	blood
45	chr8:61648400-61649000	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
46	chr8:61648400-61649200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
47	chr8:61648400-61649200	Enhancers	HUES64 Cell Line	embryonic stem cell
48	chr8:61648400-61649200	Enhancers	Gastric	stomach
49	chr8:61648400-61649200	Enhancers	Left Ventricle	heart
50	chr8:61648400-61649200	Enhancers	Stomach Mucosa	stomach

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