Variant report

Variant	rs986295
Chromosome Location	chr9:6069435-6069436
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr9:6068346..6070215-chr9:6077181..6078766,2	K562	blood:
2	chr9:6067676..6070179-chr9:6077963..6079813,2	MCF-7	breast:

Extended variants
information (count: 30 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:24)

rs_ID	r²[population]
rs10739083	0.88[AFR][1000 genomes]
rs10758741	0.89[YRI][hapmap];0.83[AFR][1000 genomes]
rs10758743	0.90[AFR][1000 genomes]
rs10975422	1.00[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs10975429	0.93[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs10975431	0.91[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs10975432	0.93[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs10975444	0.85[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs10975445	0.85[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs10975450	0.82[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs10975452	0.82[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs12377511	0.93[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs12378311	0.91[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs13287430	0.85[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs13289987	0.85[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs13290080	0.85[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs13294420	0.93[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs13299104	0.93[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs13302455	0.93[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs1576463	0.93[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs34133170	0.91[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs34916503	0.81[AFR][1000 genomes];0.93[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs35829914	0.83[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs7852365	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];0.83[ASN][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	nsv948847	chr9:5712626-6417677	Strong transcription Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	39 gene(s)	inside rSNPs	diseases
2	nsv1031086	chr9:5806949-6630686	Strong transcription Enhancers Weak transcription Active TSS Flanking Active TSS Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	42 gene(s)	inside rSNPs	diseases
3	nsv539967	chr9:5806949-6630686	Flanking Active TSS Enhancers Strong transcription Weak transcription Genic enhancers Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	42 gene(s)	inside rSNPs	diseases
4	nsv1015450	chr9:5915640-6114652	Enhancers Strong transcription Active TSS Weak transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	11 gene(s)	inside rSNPs	diseases
5	nsv613205	chr9:6032924-6332901	Flanking Active TSS Active TSS Enhancers Weak transcription ZNF genes & repeats Strong transcription Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
6	nsv916394	chr9:6055497-6322471	Enhancers Strong transcription Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:26 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:6068200-6070000	Enhancers	Primary T cells fromperipheralblood	blood
2	chr9:6068200-6070000	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
3	chr9:6068400-6070000	Enhancers	Primary monocytes fromperipheralblood	blood
4	chr9:6068400-6070000	Enhancers	Primary B cells from peripheral blood	blood
5	chr9:6068400-6070000	Enhancers	Primary T helper cells fromperipheralblood	blood
6	chr9:6068400-6070000	Enhancers	Primary T killer naive cells fromperipheralblood	blood
7	chr9:6068600-6069600	Enhancers	Primary T cells from cord blood	blood
8	chr9:6068600-6069600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
9	chr9:6068600-6069600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
10	chr9:6068600-6069600	Enhancers	Rectal Mucosa Donor 31	rectum
11	chr9:6068600-6069800	Enhancers	Primary B cells from cord blood	blood
12	chr9:6068600-6069800	Enhancers	Primary hematopoietic stem cells	blood
13	chr9:6068600-6069800	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
14	chr9:6068600-6070000	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
15	chr9:6068600-6070200	Enhancers	Rectal Mucosa Donor 29	rectum
16	chr9:6068800-6069600	Enhancers	Primary T regulatory cells fromperipheralblood	blood
17	chr9:6068800-6073000	Weak transcription	Spleen	Spleen
18	chr9:6068800-6079400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
19	chr9:6069000-6070200	Enhancers	Primary T helper naive cells from peripheral blood	blood
20	chr9:6069200-6070000	Enhancers	Primary T killer memory cells from peripheral blood	blood
21	chr9:6069400-6069600	Enhancers	Primary T helper naive cells fromperipheralblood	blood
22	chr9:6069400-6069600	Flanking Active TSS	GM12878-XiMat	blood
23	chr9:6069400-6069800	Enhancers	Monocytes-CD14+_RO01746	blood
24	chr9:6069400-6070000	Enhancers	Primary T helper cells PMA-I stimulated	--
25	chr9:6069400-6070200	Enhancers	Dnd41	blood
26	chr9:6069400-6072200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland

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