Variant report

Variant	rs13437191
Chromosome Location	chr6:27205435-27205436
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:0)
CpG islands
(count:0)
Chromatin interactive
region (count:15)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:15 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:27202802..27205636-chr6:27246312..27248576,2	K562	blood:
2	chr6:27202945..27207226-chr6:27207417..27209319,3	MCF-7	breast:
3	chr6:27203220..27205939-chr6:27245296..27248944,5	K562	blood:
4	chr6:27201132..27202809-chr6:27205095..27206707,2	MCF-7	breast:
5	chr6:27112894..27116381-chr6:27203739..27206608,3	K562	blood:
6	chr6:27197426..27201736-chr6:27203200..27207154,7	K562	blood:
7	chr6:27192628..27195388-chr6:27203355..27206168,2	K562	blood:
8	chr6:27128785..27131349-chr6:27205137..27206978,2	K562	blood:
9	chr6:27202839..27205784-chr6:27218502..27221340,2	MCF-7	breast:
10	chr6:27195411..27200167-chr6:27200252..27206108,10	K562	blood:
11	chr6:27202793..27205755-chr6:27355430..27357171,2	K562	blood:
12	chr6:27196971..27199808-chr6:27204338..27205850,2	MCF-7	breast:
13	chr6:27203048..27205771-chr6:27439622..27441138,2	K562	blood:
14	chr6:27201796..27205755-chr6:27355401..27357171,3	K562	blood:
15	chr6:27203954..27208601-chr6:27209090..27212437,6	K562	blood:

No data

Variant related genes	Relation type
ENSG00000096654	Chromatin interaction
ENSG00000265565	Chromatin interaction
ENSG00000184825	Chromatin interaction
ENSG00000112812	Chromatin interaction
ENSG00000197903	Chromatin interaction
ENSG00000124613	Chromatin interaction

Extended variants
information (count: 31 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:29)

rs_ID	r²[population]
rs11964003	0.82[CHB][hapmap];1.00[JPT][hapmap];0.81[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs11964043	0.81[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs13437532	0.86[JPT][hapmap]
rs3800308	0.94[ASN][1000 genomes]
rs3800311	1.00[JPT][hapmap]
rs3800312	0.92[CHB][hapmap];1.00[JPT][hapmap];0.81[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs3800313	0.92[CHB][hapmap];1.00[JPT][hapmap];0.81[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs4438952	0.85[CEU][hapmap]
rs4711143	0.86[JPT][hapmap]
rs4711144	0.81[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs4713077	0.81[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs5030957	0.81[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs5030960	0.82[CHB][hapmap];1.00[JPT][hapmap]
rs58336089	0.82[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs6901448	0.82[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs6902483	0.81[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs6906761	1.00[CHB][hapmap];0.93[JPT][hapmap];0.87[YRI][hapmap];0.84[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs6912503	0.92[CHB][hapmap];1.00[JPT][hapmap];0.82[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs6918423	0.82[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs6932243	1.00[CHB][hapmap];0.93[JPT][hapmap];0.84[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs6932861	0.90[CEU][hapmap];0.87[YRI][hapmap]
rs73388532	0.84[ASN][1000 genomes]
rs7755577	0.90[CEU][hapmap];1.00[CHB][hapmap];0.93[JPT][hapmap];0.86[YRI][hapmap];0.84[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs9393794	0.82[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs9461340	0.92[CHB][hapmap];1.00[JPT][hapmap];0.87[ASN][1000 genomes]
rs9468006	0.84[CHB][hapmap];0.91[JPT][hapmap]
rs9468011	0.81[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs9468014	0.92[CHB][hapmap];1.00[JPT][hapmap];0.82[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs9468016	0.81[EUR][1000 genomes];0.94[ASN][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	nsv948921	chr6:26556890-27443957	Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Flanking Active TSS Weak transcription Active TSS Enhancers Bivalent Enhancer Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	472 gene(s)	inside rSNPs	diseases
2	nsv1017328	chr6:27177147-27369588	Bivalent Enhancer Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	29 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:51 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:27199000-27205600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr6:27202800-27205600	Active TSS	HUES6 Cell Line	embryonic stem cell
3	chr6:27203400-27205600	Weak transcription	NHDF-Ad	bronchial
4	chr6:27203400-27205800	Weak transcription	HSMMtube	muscle
5	chr6:27203600-27205600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr6:27203600-27205600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
7	chr6:27203600-27205600	Weak transcription	HMEC	breast
8	chr6:27203600-27205600	Weak transcription	NHEK	skin
9	chr6:27203800-27205600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
10	chr6:27203800-27205600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
11	chr6:27204600-27205800	Active TSS	ES-I3 Cell Line	embryonic stem cell
12	chr6:27204800-27207000	Active TSS	A549	lung
13	chr6:27205000-27205600	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin03	Skin
14	chr6:27205000-27205600	Active TSS	GM12878-XiMat	blood
15	chr6:27205000-27205600	Bivalent Enhancer	HepG2	liver
16	chr6:27205000-27205800	Active TSS	H1 Cell Line	embryonic stem cell
17	chr6:27205000-27206600	Bivalent/Poised TSS	Right Ventricle	heart
18	chr6:27205000-27206800	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
19	chr6:27205000-27206800	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
20	chr6:27205000-27206800	Active TSS	HSMM	muscle
21	chr6:27205200-27205600	Active TSS	HUES48 Cell Line	embryonic stem cell
22	chr6:27205200-27205800	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
23	chr6:27205200-27205800	Active TSS	K562	blood
24	chr6:27205200-27206200	Active TSS	ES-WA7 Cell Line	embryonic stem cell
25	chr6:27205200-27206800	Bivalent Enhancer	Primary T helper 17 cells PMA-I stimulated	--
26	chr6:27205200-27207000	Bivalent/Poised TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
27	chr6:27205200-27207000	Bivalent/Poised TSS	iPS-20b Cell Line	embryonic stem cell
28	chr6:27205400-27205600	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
29	chr6:27205400-27205600	Bivalent Enhancer	Primary hematopoietic stem cells	blood
30	chr6:27205400-27205600	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
31	chr6:27205400-27205600	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Female	--
32	chr6:27205400-27205600	Bivalent/Poised TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
33	chr6:27205400-27205600	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
34	chr6:27205400-27205600	Active TSS	Osteobl	bone
35	chr6:27205400-27205800	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
36	chr6:27205400-27205800	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
37	chr6:27205400-27205800	Bivalent Enhancer	Fetal Stomach	stomach
38	chr6:27205400-27206000	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
39	chr6:27205400-27206000	Bivalent Enhancer	Primary T helper naive cells from peripheral blood	blood
40	chr6:27205400-27206000	Bivalent/Poised TSS	Brain Anterior Caudate	brain
41	chr6:27205400-27206400	Flanking Active TSS	HUVEC	blood vessel
42	chr6:27205400-27206600	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
43	chr6:27205400-27206600	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
44	chr6:27205400-27206800	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
45	chr6:27205400-27207000	Active TSS	H9 Cell Line	embryonic stem cell
46	chr6:27205400-27207000	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
47	chr6:27205400-27207000	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
48	chr6:27205400-27207000	Active TSS	NHLF	lung
49	chr6:27205400-27207200	Bivalent/Poised TSS	HUES64 Cell Line	embryonic stem cell
50	chr6:27205400-27207200	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell

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