Variant report

Variant	rs9390631
Chromosome Location	chr6:149237371-149237372
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr6:149233576..149235247-chr6:149235248..149237823,2	MCF-7	breast:
2	chr6:149236497..149238060-chr6:149238123..149240349,2	K562	blood:

Extended variants
information (count: 22 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs4333438	0.98[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9377174	1.00[CHB][hapmap];1.00[JPT][hapmap];0.84[AFR][1000 genomes];0.93[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs9377175	0.95[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9377176	1.00[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs9377177	1.00[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9390628	0.95[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.98[AFR][1000 genomes];0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs9390629	0.96[AFR][1000 genomes];0.91[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs9390630	0.83[AFR][1000 genomes];0.93[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs9390633	0.95[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];1.00[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9399670	0.95[CHB][hapmap];1.00[JPT][hapmap];0.90[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs9399671	0.96[AFR][1000 genomes];0.91[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs9399674	1.00[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs9403999	0.80[CHB][hapmap]
rs9404002	0.96[AFR][1000 genomes];0.91[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs9404003	1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[AFR][1000 genomes];0.91[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs9404005	0.81[CHB][hapmap]

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	nsv1032690	chr6:149206106-149398712	Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	11 gene(s)	inside rSNPs	diseases
2	nsv464074	chr6:149211090-149242095	Enhancers Weak transcription Strong transcription ZNF genes & repeats Flanking Active TSS Genic enhancers Bivalent Enhancer	Chromatin interactive region	n/a	inside rSNPs	diseases
3	nsv604844	chr6:149211090-149242095	Enhancers Weak transcription Strong transcription Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Genic enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases
4	nsv464075	chr6:149221294-149242095	Enhancers Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
5	nsv470865	chr6:149221294-149242095	Weak transcription Enhancers ZNF genes & repeats Strong transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
6	nsv604845	chr6:149221294-149242095	Enhancers Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:32 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:149207800-149237400	Weak transcription	H1 Cell Line	embryonic stem cell
2	chr6:149209000-149247600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr6:149210200-149240200	Weak transcription	Primary B cells from cord blood	blood
4	chr6:149211600-149255400	Weak transcription	Stomach Smooth Muscle	stomach
5	chr6:149226600-149252800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
6	chr6:149226600-149255600	Weak transcription	Ovary	ovary
7	chr6:149227400-149240400	Weak transcription	Pancreas	Pancrea
8	chr6:149230800-149238000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
9	chr6:149230800-149244600	Weak transcription	HUES48 Cell Line	embryonic stem cell
10	chr6:149231000-149244200	Weak transcription	HUES6 Cell Line	embryonic stem cell
11	chr6:149231000-149245400	Weak transcription	H9 Cell Line	embryonic stem cell
12	chr6:149234200-149244600	Weak transcription	Fetal Heart	heart
13	chr6:149234200-149245800	Weak transcription	Rectal Smooth Muscle	rectum
14	chr6:149234400-149245000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
15	chr6:149235000-149244000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
16	chr6:149235400-149253000	Weak transcription	Primary B cells from peripheral blood	blood
17	chr6:149235800-149245400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
18	chr6:149236400-149237600	Enhancers	iPS-18 Cell Line	embryonic stem cell
19	chr6:149236400-149237600	Enhancers	Liver	Liver
20	chr6:149236400-149237600	Enhancers	Fetal Lung	lung
21	chr6:149236400-149238200	Enhancers	Fetal Stomach	stomach
22	chr6:149236400-149239400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
23	chr6:149236600-149237400	Enhancers	iPS-20b Cell Line	embryonic stem cell
24	chr6:149236600-149237600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
25	chr6:149236600-149238200	Enhancers	iPS-15b Cell Line	embryonic stem cell
26	chr6:149236800-149237400	Enhancers	Cortex derived primary cultured neurospheres	brain
27	chr6:149236800-149237400	Enhancers	Fetal Kidney	kidney
28	chr6:149236800-149238200	Enhancers	ES-I3 Cell Line	embryonic stem cell
29	chr6:149237000-149237400	Enhancers	Stomach Mucosa	stomach
30	chr6:149237000-149238200	Enhancers	Fetal Brain Male	brain
31	chr6:149237000-149238600	Enhancers	HUES64 Cell Line	embryonic stem cell
32	chr6:149237000-149244600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived

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