Variant report

Variant	rs6902195
Chromosome Location	chr6:149408455-149408456
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr6:149406617..149408839-chr6:149409602..149411999,2	K562	blood:
2	chr6:149408079..149409641-chr6:149527096..149529581,2	K562	blood:
3	chr6:149402943..149406251-chr6:149407231..149409997,4	K562	blood:
4	chr6:149400900..149408936-chr6:149636750..149640736,16	MCF-7	breast:
5	chr6:149406954..149409794-chr6:149636560..149638477,3	MCF-7	breast:
6	chr6:149407215..149409434-chr6:149542169..149544216,2	K562	blood:
7	chr6:149407753..149410844-chr6:149747576..149751159,3	MCF-7	breast:

Variant related genes	Relation type
ENSG00000055208	Chromatin interaction

Extended variants
information (count: 70 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:64)

rs_ID	r²[population]
rs10457075	0.80[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs10457839	0.86[EUR][1000 genomes]
rs10457842	0.85[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs10499251	0.94[AMR][1000 genomes];0.89[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs12153925	0.80[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs12197040	0.86[EUR][1000 genomes]
rs12200909	0.80[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs12202158	0.85[EUR][1000 genomes]
rs12206419	0.83[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs12216011	0.83[EUR][1000 genomes]
rs1316376	0.91[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1316534	0.84[EUR][1000 genomes]
rs1316536	0.83[EUR][1000 genomes]
rs13190879	0.82[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs13217006	0.84[EUR][1000 genomes]
rs17669546	0.83[EUR][1000 genomes]
rs1890610	0.91[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1890612	0.91[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1934221	0.86[EUR][1000 genomes]
rs1934222	0.85[EUR][1000 genomes]
rs1934223	0.85[EUR][1000 genomes]
rs2153251	0.91[AFR][1000 genomes];0.94[AMR][1000 genomes];0.90[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2153252	0.80[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs2185250	0.91[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2340800	0.83[EUR][1000 genomes]
rs34118116	0.80[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs34599887	0.84[EUR][1000 genomes]
rs3949414	0.84[EUR][1000 genomes]
rs4313020	0.80[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs4332004	0.80[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs4336467	0.83[EUR][1000 genomes]
rs4441968	0.86[EUR][1000 genomes]
rs4454159	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6570923	0.80[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs6570924	0.85[EUR][1000 genomes]
rs6570926	0.84[EUR][1000 genomes]
rs6570927	0.84[EUR][1000 genomes]
rs6570932	0.91[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6570939	0.83[EUR][1000 genomes]
rs6901626	0.92[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6902487	0.92[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6909624	0.88[AFR][1000 genomes];0.94[AMR][1000 genomes];0.88[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs6914281	0.82[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs6914318	0.89[AMR][1000 genomes];0.87[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs6914925	0.83[EUR][1000 genomes]
rs6917010	0.89[AMR][1000 genomes];0.87[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs6924503	0.89[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs6930713	0.80[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs6932773	0.84[EUR][1000 genomes]
rs6940664	0.89[AMR][1000 genomes];0.87[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs6940915	0.89[AMR][1000 genomes];0.87[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs7762928	0.89[AMR][1000 genomes];0.87[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs7773409	0.91[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7775412	0.82[EUR][1000 genomes]
rs9322165	0.84[EUR][1000 genomes]
rs9485353	0.80[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs9498197	0.85[EUR][1000 genomes]
rs9498199	0.85[EUR][1000 genomes]
rs9498201	0.82[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs9498202	0.82[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs9498204	0.90[AFR][1000 genomes];0.94[AMR][1000 genomes];0.89[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs9498205	0.91[AFR][1000 genomes];0.94[AMR][1000 genomes];0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9498207	0.92[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9498214	0.84[EUR][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	nsv1032319	chr6:149271433-149550525	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Strong transcription Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	15 gene(s)	inside rSNPs	diseases
2	nsv538470	chr6:149271433-149550525	Enhancers Weak transcription Active TSS Strong transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	15 gene(s)	inside rSNPs	diseases
3	nsv830842	chr6:149272321-149427340	Enhancers Bivalent Enhancer ZNF genes & repeats Weak transcription Flanking Active TSS Strong transcription Genic enhancers Active TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	11 gene(s)	inside rSNPs	diseases
4	nsv1024776	chr6:149398652-149654593	Weak transcription Active TSS Bivalent Enhancer Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
5	nsv528588	chr6:149403469-149409860	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
6	esv3336182	chr6:149408141-149408698	Weak transcription	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:25 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:149395000-149415000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
2	chr6:149399200-149415000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
3	chr6:149402200-149409000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
4	chr6:149402200-149410600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
5	chr6:149402200-149414400	Weak transcription	Fetal Kidney	kidney
6	chr6:149402200-149414600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
7	chr6:149402200-149415000	Weak transcription	Esophagus	oesophagus
8	chr6:149402400-149409000	Weak transcription	Placenta Amnion	Placenta Amnion
9	chr6:149402400-149416200	Weak transcription	Fetal Heart	heart
10	chr6:149405600-149411200	Weak transcription	Primary hematopoietic stem cells	blood
11	chr6:149405600-149413000	Weak transcription	Primary T cells fromperipheralblood	blood
12	chr6:149405600-149413600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
13	chr6:149405800-149414000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
14	chr6:149406000-149409000	Weak transcription	Dnd41	blood
15	chr6:149406200-149413400	Weak transcription	Primary T helper cells fromperipheralblood	blood
16	chr6:149406200-149413600	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
17	chr6:149406800-149410600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
18	chr6:149407000-149413200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
19	chr6:149407200-149412000	Weak transcription	Primary T helper cells PMA-I stimulated	--
20	chr6:149407200-149412200	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
21	chr6:149407200-149413200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
22	chr6:149407600-149411800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
23	chr6:149407800-149409000	Weak transcription	Cortex derived primary cultured neurospheres	brain
24	chr6:149407800-149410800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
25	chr6:149407800-149411600	Weak transcription	Breast Myoepithelial Primary Cells	Breast

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