Variant report

Variant	rs9446934
Chromosome Location	chr6:74295760-74295761
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:14)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:14 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:74288220..74292842-chr6:74293561..74299022,14	K562	blood:
2	chr6:74222337..74233828-chr6:74292949..74298961,33	K562	blood:
3	chr6:74293866..74296330-chr6:74299032..74301515,2	K562	blood:
4	chr6:74224085..74235157-chr6:74287002..74297560,44	MCF-7	breast:
5	chr6:74274687..74279711-chr6:74293912..74296161,4	K562	blood:
6	chr6:74220978..74235626-chr6:74283533..74299827,68	K562	blood:
7	chr6:74295297..74298408-chr6:74308010..74309896,3	MCF-7	breast:
8	chr6:74294343..74296557-chr6:74348201..74349804,2	MCF-7	breast:
9	chr6:74294601..74296941-chr6:74314591..74316170,2	K562	blood:
10	chr6:74293523..74296291-chr6:74302711..74304704,2	K562	blood:
11	chr6:74293673..74296243-chr6:74316721..74319519,2	MCF-7	breast:
12	chr6:74287590..74292040-chr6:74293648..74296536,4	MCF-7	breast:
13	chr6:74295192..74295831-chr7:5565833..5566704,2	NB4	blood:
14	chr6:74223949..74234010-chr6:74285694..74297775,46	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000156508	Chromatin interaction
ENSG00000229862	Chromatin interaction

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

rSNPs within LD-proxies of this variant (count:22)

rs_ID	r²[population]
rs11964811	1.00[EUR][1000 genomes]
rs41265543	1.00[EUR][1000 genomes]
rs45571640	1.00[EUR][1000 genomes]
rs4708053	1.00[EUR][1000 genomes]
rs571508	1.00[EUR][1000 genomes]
rs59903417	1.00[EUR][1000 genomes]
rs6909346	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6930349	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73450693	1.00[EUR][1000 genomes]
rs73452548	1.00[EUR][1000 genomes]
rs73754635	1.00[AMR][1000 genomes]
rs73754636	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73754640	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9293936	1.00[AMR][1000 genomes]
rs9442927	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9442928	1.00[AMR][1000 genomes]
rs9446936	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9446937	1.00[EUR][1000 genomes]
rs9446956	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9446969	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9446971	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9446974	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:9 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3410973	chr6:73716033-74419545	Active TSS Bivalent Enhancer Flanking Active TSS Weak transcription Enhancers Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	191 gene(s)	inside rSNPs	diseases
2	nsv886158	chr6:74126084-74436825	Weak transcription Active TSS Strong transcription Enhancers Genic enhancers Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	179 gene(s)	inside rSNPs	diseases
3	nsv1027968	chr6:74155378-74521923	Active TSS Flanking Active TSS Strong transcription Bivalent Enhancer Weak transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	178 gene(s)	inside rSNPs	diseases
4	nsv538305	chr6:74155378-74521923	Flanking Active TSS Weak transcription Enhancers Strong transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	178 gene(s)	inside rSNPs	diseases
5	nsv1017716	chr6:74173173-74401162	Weak transcription Strong transcription Enhancers Genic enhancers Active TSS Flanking Active TSS 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 target site	170 gene(s)	inside rSNPs	diseases
6	nsv1023250	chr6:74189642-74605976	Strong transcription Weak transcription Genic enhancers Active TSS Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	172 gene(s)	inside rSNPs	diseases
7	nsv538306	chr6:74189642-74605976	Strong transcription Enhancers Active TSS Bivalent Enhancer Weak transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	172 gene(s)	inside rSNPs	diseases
8	nsv527357	chr6:74253266-74325403	Weak transcription Strong transcription Active TSS Enhancers Flanking Active TSS Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
9	nsv603694	chr6:74275405-74365807	Weak transcription Enhancers Flanking Active TSS Strong transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	17 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:121 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:74288000-74296000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
2	chr6:74289400-74302200	Weak transcription	Spleen	Spleen
3	chr6:74289400-74304000	Weak transcription	Right Ventricle	heart
4	chr6:74289600-74309600	Weak transcription	Lung	lung
5	chr6:74289600-74323800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
6	chr6:74289800-74301400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
7	chr6:74290600-74305800	Weak transcription	Fetal Muscle Trunk	muscle
8	chr6:74290600-74318400	Weak transcription	Small Intestine	intestine
9	chr6:74290600-74338800	Weak transcription	Ovary	ovary
10	chr6:74291000-74295800	Weak transcription	H9 Cell Line	embryonic stem cell
11	chr6:74291000-74307200	Weak transcription	Skeletal Muscle Male	skeletal muscle
12	chr6:74291000-74315800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
13	chr6:74291000-74323600	Weak transcription	H1 Cell Line	embryonic stem cell
14	chr6:74294800-74295800	Enhancers	Stomach Mucosa	stomach
15	chr6:74294800-74296200	Enhancers	Colonic Mucosa	Colon
16	chr6:74294800-74296400	Enhancers	Pancreas	Pancrea
17	chr6:74294800-74296600	Enhancers	Fetal Intestine Small	intestine
18	chr6:74294800-74296600	Flanking Active TSS	GM12878-XiMat	blood
19	chr6:74295000-74296000	Flanking Active TSS	Primary T helper memory cells from peripheral blood 1	blood
20	chr6:74295000-74296000	Flanking Active TSS	Rectal Smooth Muscle	rectum
21	chr6:74295000-74296000	Flanking Active TSS	HMEC	breast
22	chr6:74295000-74296200	Enhancers	Placenta Amnion	Placenta Amnion
23	chr6:74295000-74296200	Flanking Active TSS	Rectal Mucosa Donor 29	rectum
24	chr6:74295000-74296200	Flanking Active TSS	HSMMtube	muscle
25	chr6:74295000-74296400	Enhancers	iPS-15b Cell Line	embryonic stem cell
26	chr6:74295000-74296400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
27	chr6:74295000-74296400	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
28	chr6:74295000-74296400	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
29	chr6:74295000-74296400	Flanking Active TSS	Primary T helper memory cells from peripheral blood 2	blood
30	chr6:74295000-74296400	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
31	chr6:74295000-74296400	Active TSS	Aorta	Aorta
32	chr6:74295000-74296400	Flanking Active TSS	Duodenum Mucosa	Duodenum
33	chr6:74295000-74296400	Flanking Active TSS	Rectal Mucosa Donor 31	rectum
34	chr6:74295000-74296400	Flanking Active TSS	HUVEC	blood vessel
35	chr6:74295000-74296400	Flanking Active TSS	K562	blood
36	chr6:74295000-74296400	Flanking Active TSS	NHEK	skin
37	chr6:74295000-74296600	Flanking Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
38	chr6:74295000-74296600	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
39	chr6:74295000-74296600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
40	chr6:74295000-74296600	Enhancers	HUES48 Cell Line	embryonic stem cell
41	chr6:74295000-74296600	Enhancers	HUES64 Cell Line	embryonic stem cell
42	chr6:74295000-74296600	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
43	chr6:74295000-74296600	Flanking Active TSS	Muscle Satellite Cultured Cells	--
44	chr6:74295000-74296600	Flanking Active TSS	Adipose Nuclei	Adipose
45	chr6:74295000-74296600	Flanking Active TSS	Fetal Lung	lung
46	chr6:74295000-74296600	Flanking Active TSS	Hela-S3	cervix
47	chr6:74295000-74296600	Flanking Active TSS	NH-A	brain
48	chr6:74295000-74296600	Flanking Active TSS	Osteobl	bone
49	chr6:74295000-74296800	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
50	chr6:74295000-74296800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--

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