Variant report

Variant	rs9969533
Chromosome Location	chr8:90868798-90868799
allele	C/T
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:9)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:9 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr8:90867270..90880457-chr8:90913050..90918593,18	MCF-7	breast:
2	chr8:90864006..90868898-chr8:90869518..90873896,4	K562	blood:
3	chr8:90868769..90874649-chr8:90891359..90894975,5	MCF-7	breast:
4	chr8:90864006..90868898-chr8:90869518..90873802,5	K562	blood:
5	chr8:90866711..90872793-chr8:90887380..90891820,9	MCF-7	breast:
6	chr8:90737773..90739680-chr8:90867503..90870182,2	MCF-7	breast:
7	chr8:90858582..90866507-chr8:90866541..90873248,10	MCF-7	breast:
8	chr8:90855177..90868995-chr8:90994125..91001070,26	MCF-7	breast:
9	chr8:90866902..90871267-chr8:90912071..90916231,7	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000104320	Chromatin interaction
ENSG00000207359	Chromatin interaction
ENSG00000164823	Chromatin interaction

Extended variants
information (count: 40 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:37)

rs_ID	r²[population]
rs13312854	1.00[MEX][hapmap]
rs13312862	1.00[MEX][hapmap]
rs13312891	1.00[MEX][hapmap]
rs16900442	0.83[AMR][1000 genomes]
rs16900593	1.00[MEX][hapmap]
rs16900617	1.00[MEX][hapmap]
rs16900823	1.00[AMR][1000 genomes]
rs16900885	0.81[YRI][hapmap];1.00[AMR][1000 genomes]
rs16900910	0.81[YRI][hapmap];1.00[AMR][1000 genomes]
rs16900915	1.00[AMR][1000 genomes]
rs16900927	0.81[YRI][hapmap];1.00[AMR][1000 genomes]
rs16900928	0.81[YRI][hapmap];1.00[AMR][1000 genomes]
rs16900996	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs1805884	1.00[MEX][hapmap]
rs2308961	1.00[MEX][hapmap]
rs56180983	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs56729468	1.00[AMR][1000 genomes]
rs59398315	1.00[AMR][1000 genomes]
rs59483185	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs61138709	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs61327386	1.00[AMR][1000 genomes]
rs73694500	0.83[AMR][1000 genomes]
rs73696804	1.00[AMR][1000 genomes]
rs73696806	1.00[AMR][1000 genomes]
rs73696812	1.00[AMR][1000 genomes]
rs73696816	1.00[AMR][1000 genomes]
rs73696819	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73696820	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73696821	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs769417	1.00[MEX][hapmap]
rs7813347	1.00[MEX][hapmap]
rs7819919	0.80[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7822697	0.81[YRI][hapmap];0.80[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7823648	1.00[MEX][hapmap]
rs7835597	0.83[AMR][1000 genomes]
rs966597	0.81[YRI][hapmap];1.00[AMR][1000 genomes]
rs9785090	1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv933502	chr8:90702392-91049100	Weak transcription Enhancers Active TSS Strong transcription Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	62 gene(s)	inside rSNPs	diseases
2	nsv934114	chr8:90720182-90999106	Active TSS Weak transcription Enhancers Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	58 gene(s)	inside rSNPs	diseases
3	nsv891182	chr8:90785685-90888786	Flanking Active TSS Genic enhancers Weak transcription Enhancers Strong transcription ZNF genes & repeats Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:31 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:90861000-90870200	Weak transcription	HMEC	breast
2	chr8:90861000-90871000	Weak transcription	Right Atrium	heart
3	chr8:90861200-90869600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
4	chr8:90861200-90869800	Weak transcription	Rectal Smooth Muscle	rectum
5	chr8:90861400-90869000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
6	chr8:90861800-90869200	Weak transcription	Cortex derived primary cultured neurospheres	brain
7	chr8:90861800-90869200	Weak transcription	Brain Anterior Caudate	brain
8	chr8:90861800-90870200	Weak transcription	Brain Hippocampus Middle	brain
9	chr8:90864800-90870400	Weak transcription	Aorta	Aorta
10	chr8:90866600-90873400	Enhancers	HSMMtube	muscle
11	chr8:90867000-90870400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
12	chr8:90867400-90869000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
13	chr8:90867400-90869200	Enhancers	Primary B cells from cord blood	blood
14	chr8:90867400-90869200	Enhancers	Primary hematopoietic stem cells	blood
15	chr8:90867400-90869400	Enhancers	Primary B cells from peripheral blood	blood
16	chr8:90867600-90871200	Enhancers	Fetal Muscle Leg	muscle
17	chr8:90867800-90869000	Enhancers	Primary neutrophils fromperipheralblood	blood
18	chr8:90867800-90869000	Weak transcription	Fetal Muscle Trunk	muscle
19	chr8:90867800-90870200	Enhancers	A549	lung
20	chr8:90868000-90869200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
21	chr8:90868200-90869200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
22	chr8:90868200-90871200	Enhancers	Muscle Satellite Cultured Cells	--
23	chr8:90868200-90872000	Enhancers	HSMM	muscle
24	chr8:90868400-90868800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
25	chr8:90868400-90869000	Enhancers	Primary hematopoietic stem cells short term culture	blood
26	chr8:90868400-90869200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
27	chr8:90868400-90869200	Enhancers	GM12878-XiMat	blood
28	chr8:90868400-90869600	Enhancers	Ovary	ovary
29	chr8:90868400-90870200	Weak transcription	Skeletal Muscle Female	skeletal muscle
30	chr8:90868600-90868800	Enhancers	Brain Substantia Nigra	brain
31	chr8:90868600-90870200	Weak transcription	Colon Smooth Muscle	Colon

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