Variant report

Variant	rs7763272
Chromosome Location	chr6:1965568-1965569
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	GATA3	chr6:1965420-1965647	T-47D	breast:	n/a	chr6:1965537-1965545

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr6:1964426..1965970-chr6:1968700..1971465,2	K562	blood:
2	chr6:1964049..1966917-chr6:1973161..1976024,2	MCF-7	breast:

Variant related genes	Relation type
GMDS	TF binding region

Extended variants
information (count: 16 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:8)

rs_ID	r²[population]
rs11965992	1.00[YRI][hapmap];0.85[AFR][1000 genomes]
rs2449970	1.00[AMR][1000 genomes]
rs35974385	0.94[AFR][1000 genomes]
rs6596861	1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6911723	0.85[AFR][1000 genomes]
rs6919560	1.00[YRI][hapmap];0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7743218	1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7769222	1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv530548	chr6:1441421-2351608	Weak transcription Enhancers Bivalent/Poised TSS ZNF genes & repeats Flanking Active TSS Active TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	76 gene(s)	inside rSNPs	diseases
2	nsv869043	chr6:1744238-2006788	Enhancers Weak transcription ZNF genes & repeats Strong transcription Active TSS Genic enhancers Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
3	nsv931941	chr6:1768439-2246781	Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats Strong transcription Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	25 gene(s)	inside rSNPs	diseases
4	nsv531295	chr6:1773436-2724986	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	71 gene(s)	inside rSNPs	diseases
5	nsv1032149	chr6:1848148-2006021	Enhancers Active TSS Weak transcription ZNF genes & repeats Strong transcription Flanking Active TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
6	nsv1032727	chr6:1900622-2064690	Enhancers Flanking Active TSS Weak transcription Strong transcription ZNF genes & repeats Active TSS Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
7	nsv538095	chr6:1900622-2064690	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Strong transcription Genic enhancers Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
8	nsv883386	chr6:1910108-2122454	Enhancers Weak transcription Strong transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:28 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:1905000-1970600	Weak transcription	Spleen	Spleen
2	chr6:1910200-1965800	Weak transcription	Small Intestine	intestine
3	chr6:1915800-1972800	Weak transcription	Colonic Mucosa	Colon
4	chr6:1940800-1967200	Weak transcription	Primary B cells from cord blood	blood
5	chr6:1940800-1969800	Weak transcription	Lung	lung
6	chr6:1943600-1966000	Weak transcription	GM12878-XiMat	blood
7	chr6:1947400-1980000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
8	chr6:1950200-1966400	Weak transcription	Monocytes-CD14+_RO01746	blood
9	chr6:1951400-1972000	Weak transcription	Liver	Liver
10	chr6:1953400-1977800	Weak transcription	Fetal Intestine Small	intestine
11	chr6:1953600-1967200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
12	chr6:1958800-1969800	Weak transcription	Ovary	ovary
13	chr6:1959400-1965800	Weak transcription	Fetal Kidney	kidney
14	chr6:1959400-1966000	Weak transcription	Fetal Lung	lung
15	chr6:1959400-1969800	Weak transcription	Dnd41	blood
16	chr6:1961000-1965600	Weak transcription	Rectal Mucosa Donor 31	rectum
17	chr6:1961200-1970000	Weak transcription	Thymus	Thymus
18	chr6:1961200-1970400	Weak transcription	Primary T cells from cord blood	blood
19	chr6:1961200-1970600	Weak transcription	Duodenum Mucosa	Duodenum
20	chr6:1961600-1965800	Weak transcription	HepG2	liver
21	chr6:1961600-1972200	Weak transcription	Stomach Mucosa	stomach
22	chr6:1962600-1969800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
23	chr6:1962600-1970600	Weak transcription	Gastric	stomach
24	chr6:1964400-1966800	Weak transcription	Sigmoid Colon	Sigmoid Colon
25	chr6:1964600-1969600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
26	chr6:1964600-1969800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
27	chr6:1964800-1969600	Weak transcription	Primary hematopoietic stem cells	blood
28	chr6:1964800-1969800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--

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