Variant report

Variant	rs57349601
Chromosome Location	chr6:27334677-27334678
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr6:27329089..27331071-chr6:27332328..27335168,2	MCF-7	breast:
2	chr6:27334491..27337310-chr6:27338396..27341247,3	K562	blood:

Variant related genes	Relation type
ENSG00000204789	Chromatin interaction

Extended variants
information (count: 53 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:51)

rs_ID	r²[population]
rs16895205	1.00[EUR][1000 genomes]
rs16899633	1.00[EUR][1000 genomes]
rs16899664	1.00[EUR][1000 genomes]
rs16899778	1.00[EUR][1000 genomes]
rs16899794	1.00[EUR][1000 genomes]
rs16899861	1.00[EUR][1000 genomes]
rs4616979	1.00[EUR][1000 genomes]
rs5030966	1.00[EUR][1000 genomes]
rs56141585	1.00[EUR][1000 genomes]
rs56773753	1.00[EUR][1000 genomes]
rs56980568	1.00[EUR][1000 genomes]
rs56982870	1.00[EUR][1000 genomes]
rs57123722	1.00[EUR][1000 genomes]
rs57509377	1.00[EUR][1000 genomes]
rs58458505	1.00[EUR][1000 genomes]
rs58669069	1.00[EUR][1000 genomes]
rs58685987	1.00[EUR][1000 genomes]
rs58942357	1.00[EUR][1000 genomes]
rs59659183	1.00[EUR][1000 genomes]
rs59813908	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs59886985	1.00[EUR][1000 genomes]
rs61137579	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs61206558	1.00[EUR][1000 genomes]
rs61482673	1.00[EUR][1000 genomes]
rs61483696	1.00[EUR][1000 genomes]
rs61740349	1.00[EUR][1000 genomes]
rs73738714	1.00[EUR][1000 genomes]
rs73738743	1.00[EUR][1000 genomes]
rs73738764	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73738772	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73738775	1.00[EUR][1000 genomes]
rs73738795	1.00[EUR][1000 genomes]
rs73738796	1.00[EUR][1000 genomes]
rs73738798	1.00[EUR][1000 genomes]
rs73738799	1.00[EUR][1000 genomes]
rs73738802	1.00[EUR][1000 genomes]
rs73739106	1.00[EUR][1000 genomes]
rs73740430	1.00[EUR][1000 genomes]
rs73741704	1.00[EUR][1000 genomes]
rs73741705	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73741706	1.00[EUR][1000 genomes]
rs73741716	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs766093	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7744655	1.00[EUR][1000 genomes]
rs7750919	1.00[EUR][1000 genomes]
rs7751102	1.00[EUR][1000 genomes]
rs7758568	1.00[EUR][1000 genomes]
rs7765353	1.00[EUR][1000 genomes]
rs7768826	1.00[EUR][1000 genomes]
rs7773166	1.00[EUR][1000 genomes]
rs7775305	1.00[EUR][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:50 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:27316800-27335400	Weak transcription	Pancreas	Pancrea
2	chr6:27325800-27336200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
3	chr6:27326000-27335600	Weak transcription	Brain Germinal Matrix	brain
4	chr6:27326800-27342000	Weak transcription	Colonic Mucosa	Colon
5	chr6:27327000-27342000	Weak transcription	Brain Cingulate Gyrus	brain
6	chr6:27327400-27335600	Weak transcription	Gastric	stomach
7	chr6:27327400-27335800	Weak transcription	H9 Cell Line	embryonic stem cell
8	chr6:27327400-27336600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
9	chr6:27327400-27341800	Weak transcription	Fetal Brain Male	brain
10	chr6:27327400-27341800	Weak transcription	Fetal Kidney	kidney
11	chr6:27327600-27335800	Weak transcription	Brain Angular Gyrus	brain
12	chr6:27327600-27342200	Weak transcription	Brain Substantia Nigra	brain
13	chr6:27328000-27335600	Weak transcription	Rectal Smooth Muscle	rectum
14	chr6:27328000-27342400	Weak transcription	Sigmoid Colon	Sigmoid Colon
15	chr6:27328200-27335800	Weak transcription	Right Ventricle	heart
16	chr6:27328200-27341800	Weak transcription	Adipose Nuclei	Adipose
17	chr6:27328200-27341800	Weak transcription	Brain Hippocampus Middle	brain
18	chr6:27328200-27341800	Weak transcription	Skeletal Muscle Female	skeletal muscle
19	chr6:27328200-27342200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
20	chr6:27328400-27335200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
21	chr6:27328400-27341800	Weak transcription	Rectal Mucosa Donor 31	rectum
22	chr6:27329200-27335600	Weak transcription	Skeletal Muscle Male	skeletal muscle
23	chr6:27329400-27335400	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
24	chr6:27329400-27337000	Strong transcription	Breast Myoepithelial Primary Cells	Breast
25	chr6:27329400-27341800	Weak transcription	Placenta Amnion	Placenta Amnion
26	chr6:27329600-27335600	Weak transcription	Lung	lung
27	chr6:27329800-27335000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
28	chr6:27329800-27335600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
29	chr6:27329800-27335600	Weak transcription	Brain Inferior Temporal Lobe	brain
30	chr6:27329800-27342000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
31	chr6:27330200-27335600	Weak transcription	Fetal Stomach	stomach
32	chr6:27330200-27341400	Weak transcription	Pancreatic Islets	Pancreatic Islet
33	chr6:27330600-27335600	Weak transcription	HUES64 Cell Line	embryonic stem cell
34	chr6:27330600-27341800	Weak transcription	H1 Cell Line	embryonic stem cell
35	chr6:27330600-27341800	Weak transcription	Brain Anterior Caudate	brain
36	chr6:27331200-27335600	Weak transcription	Colon Smooth Muscle	Colon
37	chr6:27331200-27335600	Weak transcription	Duodenum Smooth Muscle	Duodenum
38	chr6:27331200-27335600	Weak transcription	Fetal Lung	lung
39	chr6:27331200-27335800	Weak transcription	Primary T helper cells fromperipheralblood	blood
40	chr6:27331200-27341600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
41	chr6:27331200-27341800	Weak transcription	Rectal Mucosa Donor 29	rectum
42	chr6:27331400-27335400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
43	chr6:27331600-27335200	Weak transcription	Ovary	ovary
44	chr6:27331600-27342000	Weak transcription	Left Ventricle	heart
45	chr6:27333600-27336800	Strong transcription	Stomach Smooth Muscle	stomach
46	chr6:27334000-27335000	Weak transcription	HUES6 Cell Line	embryonic stem cell
47	chr6:27334000-27341400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
48	chr6:27334000-27342200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
49	chr6:27334400-27336000	Weak transcription	Fetal Brain Female	brain
50	chr6:27334600-27335600	Weak transcription	Aorta	Aorta

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