Variant report

Variant	rs7754647
Chromosome Location	chr6:11371915-11371916
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	chr6:11371466..11375840-chr6:11379276..11384937,6	MCF-7	breast:

Variant related genes	Relation type
ENSG00000111859	Chromatin interaction

Extended variants
information (count: 19 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs10947217	0.86[YRI][hapmap]
rs11756278	0.91[YRI][hapmap]
rs17507230	0.83[YRI][hapmap]
rs4711275	0.86[EUR][1000 genomes]
rs4711276	0.85[EUR][1000 genomes]
rs4713483	0.86[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs4713486	0.86[EUR][1000 genomes]
rs4713487	0.85[EUR][1000 genomes]
rs6916980	0.85[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs738271	0.83[CHB][hapmap]
rs7740502	0.87[YRI][hapmap]
rs7741863	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7750329	0.83[CHB][hapmap]
rs7775262	0.83[CHB][hapmap]
rs9469022	0.96[CEU][hapmap];1.00[CHB][hapmap];0.92[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs9469044	0.86[EUR][1000 genomes];0.85[ASN][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	nsv1021078	chr6:10819083-11558560	Enhancers Strong transcription Active TSS Flanking Active TSS Weak transcription Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	47 gene(s)	inside rSNPs	diseases
2	nsv538135	chr6:10819083-11558560	Weak transcription Enhancers Strong transcription Flanking Active TSS Bivalent Enhancer Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	47 gene(s)	inside rSNPs	diseases
3	nsv432848	chr6:11371614-11560114	Enhancers Active TSS Weak transcription ZNF genes & repeats Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:41 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:11364600-11381200	Enhancers	Primary monocytes fromperipheralblood	blood
2	chr6:11365600-11374400	Weak transcription	Stomach Mucosa	stomach
3	chr6:11365600-11374800	Weak transcription	Primary hematopoietic stem cells	blood
4	chr6:11367600-11372000	Weak transcription	Rectal Smooth Muscle	rectum
5	chr6:11368400-11373800	Weak transcription	Rectal Mucosa Donor 29	rectum
6	chr6:11368400-11374400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
7	chr6:11368400-11374400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
8	chr6:11368400-11374600	Weak transcription	Rectal Mucosa Donor 31	rectum
9	chr6:11368800-11376800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
10	chr6:11369000-11380200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
11	chr6:11369200-11374400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
12	chr6:11369200-11374600	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
13	chr6:11369400-11373600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
14	chr6:11370000-11372000	Genic enhancers	Primary T helper cells PMA-I stimulated	--
15	chr6:11370200-11374000	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
16	chr6:11370200-11374400	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
17	chr6:11370800-11372000	ZNF genes & repeats	GM12878-XiMat	blood
18	chr6:11371200-11372800	Enhancers	Monocytes-CD14+_RO01746	blood
19	chr6:11371200-11373600	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
20	chr6:11371200-11374000	Weak transcription	Sigmoid Colon	Sigmoid Colon
21	chr6:11371200-11374400	Weak transcription	Colonic Mucosa	Colon
22	chr6:11371200-11374400	Weak transcription	Left Ventricle	heart
23	chr6:11371200-11374400	Weak transcription	Thymus	Thymus
24	chr6:11371200-11374600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
25	chr6:11371200-11374600	Weak transcription	Gastric	stomach
26	chr6:11371200-11375800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
27	chr6:11371200-11376600	Weak transcription	Adipose Nuclei	Adipose
28	chr6:11371200-11377000	Weak transcription	Lung	lung
29	chr6:11371200-11378400	Weak transcription	Fetal Thymus	thymus
30	chr6:11371200-11380200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
31	chr6:11371400-11373800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
32	chr6:11371400-11374000	Weak transcription	Primary T cells fromperipheralblood	blood
33	chr6:11371400-11374000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
34	chr6:11371400-11376800	Weak transcription	Placenta	Placenta
35	chr6:11371400-11377000	Weak transcription	Spleen	Spleen
36	chr6:11371600-11372600	Weak transcription	Primary B cells from peripheral blood	blood
37	chr6:11371600-11373800	Weak transcription	Primary T cells from cord blood	blood
38	chr6:11371600-11374000	Weak transcription	Primary T helper cells fromperipheralblood	blood
39	chr6:11371800-11372000	Genic enhancers	Primary B cells from cord blood	blood
40	chr6:11371800-11372200	Weak transcription	Primary neutrophils fromperipheralblood	blood
41	chr6:11371800-11373600	Weak transcription	HepG2	liver

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