Variant report

Variant	rs368611940
Chromosome Location	chr1:92211205-92211206
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr1:92076490..92078813-chr1:92209944..92211883,2	K562	blood:
2	chr1:92207551..92212491-chr1:92212891..92216237,4	K562	blood:

Extended variants
information (count: 8 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1009560	chr1:91897078-92270781	Enhancers Strong transcription Bivalent Enhancer Weak transcription Flanking Active TSS Genic enhancers Active TSS ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	14 gene(s)	inside rSNPs	diseases
2	nsv1012864	chr1:92067100-92827761	Flanking Active TSS Strong transcription Enhancers Active TSS Weak transcription Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	33 gene(s)	inside rSNPs	diseases
3	nsv535029	chr1:92067100-92827761	Strong transcription Weak transcription Enhancers Active TSS Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	33 gene(s)	inside rSNPs	diseases
4	nsv530438	chr1:92091957-92827760	Weak transcription Active TSS Strong transcription Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	33 gene(s)	inside rSNPs	diseases
5	nsv1010179	chr1:92140209-92655952	Weak transcription Genic enhancers Flanking Active TSS Enhancers Strong transcription Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	19 gene(s)	inside rSNPs	diseases
6	nsv535030	chr1:92140209-92655952	Enhancers Weak transcription Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Strong transcription ZNF genes & repeats Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	19 gene(s)	inside rSNPs	diseases
7	nsv1005917	chr1:92189945-92378683	Flanking Active TSS Enhancers Weak transcription Genic enhancers Strong transcription Active TSS Bivalent Enhancer 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	4 gene(s)	inside rSNPs	diseases
8	nsv949449	chr1:92211020-92585831	Strong transcription Enhancers Genic enhancers Weak transcription Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	14 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	chr1:92197000-92215200	Weak transcription	Brain Inferior Temporal Lobe	brain
2	chr1:92197200-92215400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
3	chr1:92197600-92230000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
4	chr1:92198200-92224400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
5	chr1:92199200-92218600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
6	chr1:92199400-92219000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
7	chr1:92201200-92219000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
8	chr1:92201400-92217600	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
9	chr1:92203200-92212800	Weak transcription	Spleen	Spleen
10	chr1:92204800-92247000	Weak transcription	Primary T helper cells fromperipheralblood	blood
11	chr1:92205000-92212400	Weak transcription	Pancreatic Islets	Pancreatic Islet
12	chr1:92206200-92212000	Enhancers	Colon Smooth Muscle	Colon
13	chr1:92206200-92212400	Weak transcription	H1 Cell Line	embryonic stem cell
14	chr1:92206200-92213600	Genic enhancers	Breast Myoepithelial Primary Cells	Breast
15	chr1:92207600-92211400	Enhancers	Skeletal Muscle Male	skeletal muscle
16	chr1:92208400-92235800	Weak transcription	Rectal Mucosa Donor 29	rectum
17	chr1:92208800-92212600	Weak transcription	Lung	lung
18	chr1:92208800-92214800	Weak transcription	Brain Substantia Nigra	brain
19	chr1:92209000-92212400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
20	chr1:92209000-92212400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
21	chr1:92209000-92212400	Weak transcription	Fetal Muscle Trunk	muscle
22	chr1:92209200-92212400	Weak transcription	Muscle Satellite Cultured Cells	--
23	chr1:92209200-92212600	Weak transcription	NHLF	lung
24	chr1:92209200-92215600	Weak transcription	Osteobl	bone
25	chr1:92209200-92217000	Weak transcription	Primary T cells fromperipheralblood	blood
26	chr1:92209400-92212600	Weak transcription	Left Ventricle	heart
27	chr1:92209400-92213400	Weak transcription	Psoas Muscle	Psoas
28	chr1:92209600-92212200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
29	chr1:92209600-92212400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
30	chr1:92209800-92211800	Enhancers	Fetal Muscle Leg	muscle
31	chr1:92210000-92211400	Enhancers	Skeletal Muscle Female	skeletal muscle
32	chr1:92210000-92211800	Enhancers	Fetal Kidney	kidney
33	chr1:92210000-92212000	Enhancers	Adipose Nuclei	Adipose
34	chr1:92210200-92211600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
35	chr1:92210200-92211800	Enhancers	Brain Anterior Caudate	brain
36	chr1:92210200-92212200	Enhancers	NHEK	skin
37	chr1:92210400-92211400	Flanking Active TSS	Liver	Liver
38	chr1:92210400-92211400	Enhancers	Brain Angular Gyrus	brain
39	chr1:92210400-92211400	Enhancers	Fetal Heart	heart
40	chr1:92210400-92211800	Enhancers	Pancreas	Pancrea
41	chr1:92210400-92212000	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
42	chr1:92210400-92212000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
43	chr1:92210400-92212000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
44	chr1:92210400-92212000	Enhancers	Right Atrium	heart
45	chr1:92210400-92212200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
46	chr1:92210400-92213400	Enhancers	Fetal Lung	lung
47	chr1:92210600-92211600	Enhancers	Brain Germinal Matrix	brain
48	chr1:92210600-92213600	Weak transcription	Right Ventricle	heart
49	chr1:92210800-92211400	Enhancers	Small Intestine	intestine
50	chr1:92210800-92212600	Weak transcription	Placenta	Placenta

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