Variant report

Variant	rs884136
Chromosome Location	chr8:58979293-58979294
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:0)
CpG islands
(count:61)
Chromatin interactive
region (count:4)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:58979272-58979322	HPAEpiC	pulmonary alveolar:	n/a
2	chr8:58979272-58979322	AG09309	skin:	n/a
3	chr8:58979272-58979322	NHDF-neo	bronchial:	n/a
4	chr8:58979272-58979322	T-47D	breast:	n/a
5	chr8:58979272-58979322	HCPEpiC	choroid plexus:	n/a
6	chr8:58979272-58979322	Jurkat	blood:	n/a
7	chr8:58979272-58979322	RPTEC	kidney:	n/a
8	chr8:58979272-58979322	SKMC	muscle:	n/a
9	chr8:58979272-58979322	GM19239	blood:	n/a
10	chr8:58979272-58979322	SK-N-SH	brain:	n/a
11	chr8:58979272-58979322	U87	brain:	n/a
12	chr8:58979272-58979322	AG10803	skin:	n/a
13	chr8:58979272-58979322	Hepatocyte	liver:	n/a
14	chr8:58979272-58979322	HAEpiC	amniotic membrane:	n/a
15	chr8:58979272-58979322	A549	lung:	n/a
16	chr8:58979272-58979322	SK-N-SH_RA	brain:	n/a
17	chr8:58979272-58979322	HNPCEpiC	eye:	n/a
18	chr8:58979272-58979322	ovcar-3	ovarian:	n/a
19	chr8:58979272-58979322	GM06990	blood:	n/a
20	chr8:58979272-58979322	PFSK-1	brain:	n/a
21	chr8:58979272-58979322	HCF	heart:	n/a
22	chr8:58979272-58979322	Hela-S3	cervix:	n/a
23	chr8:58979272-58979322	IMR90	lung:	fetal
24	chr8:58979272-58979322	AG04449	skin:	fetal
25	chr8:58979272-58979322	NB4	blood:	n/a
26	chr8:58979272-58979322	NT2-D1	testis:	n/a
27	chr8:58979272-58979322	HRCEpiC	kidney:	n/a
28	chr8:58979272-58979322	GM12892	blood:	n/a
29	chr8:58979272-58979322	MCF-7	breast:	n/a
30	chr8:58979272-58979322	AG09319	gingival:	n/a
31	chr8:58979272-58979322	AoSMC	blood vessel:	n/a
32	chr8:58979272-58979322	HL-60	blood:	n/a
33	chr8:58979272-58979322	HCM	heart:	n/a
34	chr8:58979272-58979322	HRPEpiC	eye:	n/a
35	chr8:58979272-58979322	BJ	skin:	n/a
36	chr8:58979272-58979322	SAEC	small airway:	n/a
37	chr8:58979272-58979322	PANC-1	pancreas:	n/a
38	chr8:58979272-58979322	SK-N-MC	brain:	n/a
39	chr8:58979272-58979322	NHBE	bronchial:	n/a
40	chr8:58979272-58979322	PrEC	prostate:	n/a
41	chr8:58979272-58979322	H1-hESC	embryonic stem cell:	embryo
42	chr8:58979272-58979322	AG04450	lung:	fetal
43	chr8:58979272-58979322	CMK	blood:	n/a
44	chr8:58979272-58979322	Caco-2	colon:	n/a
45	chr8:58979272-58979322	BE2_C	brain:	n/a
46	chr8:58979272-58979322	MCF10A-Er-Src	breast:	n/a
47	chr8:58979272-58979322	HMEC	breast:	n/a
48	chr8:58979272-58979322	HIPEpiC	eye:	n/a
49	chr8:58979272-58979322	GM12891	blood:	n/a
50	chr8:58979272-58979322	HepG2	liver:	n/a

(count:4 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr8:58972227..58973828-chr8:58977965..58980354,2	MCF-7	breast:
2	chr8:58973927..58975481-chr8:58979211..58981021,2	K562	blood:
3	chr8:58964702..58966209-chr8:58978856..58981572,2	K562	blood:
4	chr8:58979230..58980915-chr8:59145278..59146797,2	MCF-7	breast:

No data

Variant related genes	Relation type
FAM110B	CpG island

Extended variants
information (count: 58 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:56)

rs_ID	r²[population]
rs10089259	0.85[CEU][hapmap]
rs10110195	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs10957030	1.00[CEU][hapmap];1.00[CHB][hapmap];0.80[YRI][hapmap];1.00[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1108188	0.85[CEU][hapmap]
rs11774174	1.00[CEU][hapmap];1.00[CHB][hapmap];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11781102	1.00[CEU][hapmap];1.00[CHB][hapmap];0.85[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11781204	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[YRI][hapmap];0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11997733	0.85[CEU][hapmap]
rs11998721	1.00[CEU][hapmap];1.00[CHB][hapmap];0.92[YRI][hapmap];1.00[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12114432	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]
rs16922937	1.00[CEU][hapmap];1.00[CHB][hapmap];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16922943	1.00[CEU][hapmap];1.00[CHB][hapmap];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16922946	1.00[CEU][hapmap];1.00[CHB][hapmap];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16923114	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs28508605	1.00[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56288562	1.00[ASN][1000 genomes]
rs57550641	1.00[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs58595014	0.83[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs59166085	1.00[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs60139253	1.00[ASN][1000 genomes]
rs61521318	1.00[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6471679	1.00[CEU][hapmap];1.00[CHB][hapmap];0.97[EUR][1000 genomes]
rs6989882	1.00[CEU][hapmap];1.00[CHB][hapmap];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7000941	1.00[CEU][hapmap];1.00[CHB][hapmap];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7007800	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]
rs7015049	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73236447	1.00[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73236448	1.00[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73236451	0.92[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73236452	0.92[AMR][1000 genomes];0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73236455	0.92[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73236458	0.92[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73236461	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73236476	1.00[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73236481	1.00[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73236484	0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73236488	0.83[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs73236490	0.83[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs73241723	0.83[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs73682130	1.00[ASN][1000 genomes]
rs73682133	1.00[ASN][1000 genomes]
rs73682134	1.00[ASN][1000 genomes]
rs73682136	1.00[ASN][1000 genomes]
rs73682137	1.00[ASN][1000 genomes]
rs73682138	1.00[ASN][1000 genomes]
rs73682140	1.00[ASN][1000 genomes]
rs73682141	1.00[ASN][1000 genomes]
rs73682142	1.00[ASN][1000 genomes]
rs7812600	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7813490	0.85[CEU][hapmap]
rs7816440	1.00[CHB][hapmap];0.83[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs7828423	0.85[CEU][hapmap]
rs7832353	0.85[CEU][hapmap]
rs884135	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]
rs9694113	1.00[CEU][hapmap];1.00[CHB][hapmap];0.92[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9694139	1.00[CEU][hapmap];1.00[CHB][hapmap];0.92[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv831324	chr8:58844151-59045309	Flanking Active TSS Weak transcription Enhancers Genic enhancers Strong transcription Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
2	esv1803360	chr8:58976889-58986166	Weak transcription Enhancers Active TSS Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	n/a

No data

Chromatin state (count:63 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:58935600-58988800	Weak transcription	Aorta	Aorta
2	chr8:58952200-58986400	Weak transcription	Adipose Nuclei	Adipose
3	chr8:58952800-58979600	Weak transcription	HSMMtube	muscle
4	chr8:58966600-58980000	Weak transcription	Ovary	ovary
5	chr8:58968800-58981000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
6	chr8:58969800-58979800	Weak transcription	HSMM	muscle
7	chr8:58971200-58982800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
8	chr8:58973200-58979800	Weak transcription	Pancreatic Islets	Pancreatic Islet
9	chr8:58973600-58982600	Weak transcription	Spleen	Spleen
10	chr8:58974000-58979800	Weak transcription	NHLF	lung
11	chr8:58974400-58979600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
12	chr8:58974400-58979600	Weak transcription	NHDF-Ad	bronchial
13	chr8:58974600-58979400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
14	chr8:58975800-58982600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
15	chr8:58977200-58980400	Enhancers	Fetal Heart	heart
16	chr8:58977400-58981200	Enhancers	Cortex derived primary cultured neurospheres	brain
17	chr8:58977600-58980200	Enhancers	Fetal Kidney	kidney
18	chr8:58977600-58981400	Enhancers	Fetal Lung	lung
19	chr8:58978200-58981400	Enhancers	Liver	Liver
20	chr8:58978400-58979600	Genic enhancers	Fetal Stomach	stomach
21	chr8:58978400-58980600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
22	chr8:58978400-58980800	Enhancers	HUES6 Cell Line	embryonic stem cell
23	chr8:58978400-58980800	Enhancers	Brain Germinal Matrix	brain
24	chr8:58978600-58979600	Enhancers	Lung	lung
25	chr8:58978600-58980000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
26	chr8:58978600-58980200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
27	chr8:58978600-58980400	Weak transcription	Placenta Amnion	Placenta Amnion
28	chr8:58978600-58980400	Enhancers	Right Atrium	heart
29	chr8:58978600-58980600	Enhancers	ES-I3 Cell Line	embryonic stem cell
30	chr8:58978600-58981200	Enhancers	Colon Smooth Muscle	Colon
31	chr8:58978600-58982200	Enhancers	HepG2	liver
32	chr8:58978800-58979400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
33	chr8:58978800-58979600	Genic enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
34	chr8:58978800-58979600	Enhancers	Placenta	Placenta
35	chr8:58978800-58980200	Enhancers	Fetal Muscle Trunk	muscle
36	chr8:58978800-58980200	Enhancers	Gastric	stomach
37	chr8:58978800-58980200	Enhancers	Left Ventricle	heart
38	chr8:58978800-58980200	Enhancers	Right Ventricle	heart
39	chr8:58978800-58980800	Enhancers	Brain Anterior Caudate	brain
40	chr8:58978800-58981000	Enhancers	Brain Hippocampus Middle	brain
41	chr8:58978800-58981200	Enhancers	Duodenum Smooth Muscle	Duodenum
42	chr8:58978800-58982600	Enhancers	Fetal Brain Male	brain
43	chr8:58978800-58982600	Enhancers	Skeletal Muscle Female	skeletal muscle
44	chr8:58979000-58979400	Genic enhancers	Fetal Muscle Leg	muscle
45	chr8:58979000-58979800	Weak transcription	Brain Substantia Nigra	brain
46	chr8:58979000-58979800	Weak transcription	Pancreas	Pancrea
47	chr8:58979000-58980000	Weak transcription	H1 Cell Line	embryonic stem cell
48	chr8:58979000-58980000	Weak transcription	Psoas Muscle	Psoas
49	chr8:58979000-58980200	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
50	chr8:58979000-58980200	Enhancers	GM12878-XiMat	blood

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