Variant report

Variant	rs6910667
Chromosome Location	chr6:11325078-11325079
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr6:11319797..11323396-chr6:11323814..11327323,3	K562	blood:
2	chr6:11324284..11325919-chr6:11331511..11333419,2	K562	blood:
3	chr6:11321749..11324194-chr6:11324346..11326664,2	MCF-7	breast:
4	chr6:11230728..11233770-chr6:11322053..11325957,3	MCF-7	breast:
5	chr6:11323888..11326664-chr6:11327158..11331364,4	MCF-7	breast:

Variant related genes	Relation type
ENSG00000111859	Chromatin interaction

Extended variants
information (count: 4 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:2)

rs_ID	r²[population]
rs16871252	1.00[MEX][hapmap]
rs16871254	1.00[LWK][hapmap];1.00[MEX][hapmap];0.83[MKK][hapmap];1.00[YRI][hapmap];0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 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

No data

Chromatin state (count:67 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:11306400-11326800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
2	chr6:11316200-11329800	Weak transcription	Right Atrium	heart
3	chr6:11319400-11330600	Weak transcription	Duodenum Smooth Muscle	Duodenum
4	chr6:11319600-11328000	Weak transcription	Small Intestine	intestine
5	chr6:11319600-11328200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
6	chr6:11319600-11330000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
7	chr6:11319600-11330400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
8	chr6:11319800-11328800	Weak transcription	Rectal Mucosa Donor 31	rectum
9	chr6:11319800-11330600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
10	chr6:11319800-11330800	Weak transcription	Fetal Stomach	stomach
11	chr6:11320000-11328400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
12	chr6:11320000-11329800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
13	chr6:11320000-11330200	Weak transcription	Gastric	stomach
14	chr6:11320000-11330600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
15	chr6:11320200-11327400	Weak transcription	Primary T helper cells fromperipheralblood	blood
16	chr6:11320200-11328000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
17	chr6:11320200-11329600	Weak transcription	Duodenum Mucosa	Duodenum
18	chr6:11320200-11329800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
19	chr6:11320200-11330600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
20	chr6:11320400-11329000	Weak transcription	Fetal Muscle Leg	muscle
21	chr6:11320400-11329400	Weak transcription	Pancreas	Pancrea
22	chr6:11321400-11325200	Enhancers	Breast Myoepithelial Primary Cells	Breast
23	chr6:11321600-11325200	Enhancers	A549	lung
24	chr6:11322400-11325600	Enhancers	Primary monocytes fromperipheralblood	blood
25	chr6:11322600-11325600	Enhancers	Fetal Intestine Large	intestine
26	chr6:11322600-11327200	Enhancers	HepG2	liver
27	chr6:11322600-11331200	Enhancers	Placenta	Placenta
28	chr6:11322800-11325400	Genic enhancers	Primary B cells from cord blood	blood
29	chr6:11323000-11325200	Enhancers	Primary hematopoietic stem cells	blood
30	chr6:11323000-11328600	Weak transcription	NH-A	brain
31	chr6:11323600-11325400	Enhancers	Fetal Intestine Small	intestine
32	chr6:11323800-11325600	Enhancers	Fetal Thymus	thymus
33	chr6:11324400-11325200	Enhancers	H1 Cell Line	embryonic stem cell
34	chr6:11324400-11325400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
35	chr6:11324400-11325400	Genic enhancers	Primary T cells from cord blood	blood
36	chr6:11324400-11326000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
37	chr6:11324400-11326000	Enhancers	Primary T helper cells PMA-I stimulated	--
38	chr6:11324400-11329200	Weak transcription	Colonic Mucosa	Colon
39	chr6:11324400-11329400	Weak transcription	Stomach Mucosa	stomach
40	chr6:11324600-11325400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
41	chr6:11324600-11325400	Enhancers	Thymus	Thymus
42	chr6:11324600-11326200	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
43	chr6:11324600-11328200	Weak transcription	Placenta Amnion	Placenta Amnion
44	chr6:11324600-11329200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
45	chr6:11324600-11329200	Weak transcription	Adipose Nuclei	Adipose
46	chr6:11324800-11325200	Enhancers	ES-I3 Cell Line	embryonic stem cell
47	chr6:11324800-11325200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
48	chr6:11324800-11325200	Enhancers	iPS-18 Cell Line	embryonic stem cell
49	chr6:11324800-11325200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
50	chr6:11324800-11325400	Enhancers	Primary T cells fromperipheralblood	blood

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