Variant report

Variant	rs34761930
Chromosome Location	chr1:151089523-151089524
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr1:151040835..151043433-chr1:151088012..151090522,2	K562	blood:
2	chr1:151089435..151091250-chr1:151117616..151120097,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000143434	Chromatin interaction
ENSG00000143458	Chromatin interaction
ENSG00000197622	Chromatin interaction

Extended variants
information (count: 19 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:14)

rs_ID	r²[population]
rs11204774	0.89[AFR][1000 genomes];0.89[EUR][1000 genomes]
rs11204775	0.85[EUR][1000 genomes]
rs11204783	0.83[AFR][1000 genomes]
rs12058128	1.00[AFR][1000 genomes];0.83[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs12060682	0.89[EUR][1000 genomes]
rs12070256	0.89[EUR][1000 genomes]
rs12074309	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12088941	0.89[EUR][1000 genomes]
rs12090246	1.00[AFR][1000 genomes];0.83[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs16832976	0.81[AFR][1000 genomes]
rs3892218	0.85[AFR][1000 genomes];0.89[EUR][1000 genomes]
rs59603391	0.87[EUR][1000 genomes]
rs6587556	0.89[AFR][1000 genomes]
rs7537292	0.82[AFR][1000 genomes];0.89[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1001897	chr1:150743271-151241600	Flanking Active TSS Enhancers Weak transcription Active TSS Strong transcription Genic 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	156 gene(s)	inside rSNPs	diseases
2	nsv535158	chr1:150743271-151241600	Genic enhancers Weak transcription Strong transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	156 gene(s)	inside rSNPs	diseases
3	nsv522840	chr1:150933723-151347746	Weak transcription Strong transcription Genic enhancers Flanking Active TSS Enhancers Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	169 gene(s)	inside rSNPs	diseases
4	nsv916272	chr1:150961809-151557253	Weak transcription Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Active TSS Genic enhancers Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	219 gene(s)	inside rSNPs	diseases
5	nsv872421	chr1:151055670-151098077	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:96 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:151044400-151090200	Weak transcription	Gastric	stomach
2	chr1:151044400-151090400	Weak transcription	Right Ventricle	heart
3	chr1:151044400-151103600	Weak transcription	Small Intestine	intestine
4	chr1:151044800-151098800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
5	chr1:151047200-151090400	Weak transcription	Dnd41	blood
6	chr1:151047400-151090400	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
7	chr1:151052200-151103000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
8	chr1:151060600-151090200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
9	chr1:151061800-151090400	Weak transcription	Fetal Kidney	kidney
10	chr1:151061800-151105600	Weak transcription	Cortex derived primary cultured neurospheres	brain
11	chr1:151064200-151103400	Weak transcription	Colonic Mucosa	Colon
12	chr1:151067000-151103400	Weak transcription	Fetal Brain Male	brain
13	chr1:151068400-151090400	Weak transcription	Pancreas	Pancrea
14	chr1:151071400-151090400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
15	chr1:151072400-151091400	Weak transcription	Fetal Lung	lung
16	chr1:151074000-151101000	Weak transcription	Fetal Heart	heart
17	chr1:151077800-151090400	Weak transcription	Rectal Smooth Muscle	rectum
18	chr1:151078000-151096400	Strong transcription	Fetal Intestine Small	intestine
19	chr1:151079200-151093800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
20	chr1:151079600-151090400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
21	chr1:151079600-151091400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
22	chr1:151079600-151096400	Weak transcription	Hela-S3	cervix
23	chr1:151079800-151089800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
24	chr1:151079800-151091600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
25	chr1:151079800-151097000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
26	chr1:151079800-151102000	Weak transcription	NHDF-Ad	bronchial
27	chr1:151079800-151103400	Weak transcription	NH-A	brain
28	chr1:151079800-151103400	Weak transcription	NHEK	skin
29	chr1:151079800-151103400	Weak transcription	NHLF	lung
30	chr1:151079800-151106200	Weak transcription	HSMMtube	muscle
31	chr1:151079800-151114800	Weak transcription	HSMM	muscle
32	chr1:151080000-151090600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
33	chr1:151080600-151090400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
34	chr1:151081000-151100800	Weak transcription	Rectal Mucosa Donor 31	rectum
35	chr1:151081200-151089800	Weak transcription	Brain Cingulate Gyrus	brain
36	chr1:151081200-151089800	Weak transcription	Placenta Amnion	Placenta Amnion
37	chr1:151081200-151090200	Weak transcription	Esophagus	oesophagus
38	chr1:151081200-151090400	Weak transcription	Primary neutrophils fromperipheralblood	blood
39	chr1:151081200-151090400	Weak transcription	Brain Substantia Nigra	brain
40	chr1:151081200-151090400	Weak transcription	Lung	lung
41	chr1:151081200-151095000	Weak transcription	Aorta	Aorta
42	chr1:151081200-151102000	Weak transcription	Brain Germinal Matrix	brain
43	chr1:151081200-151103400	Weak transcription	GM12878-XiMat	blood
44	chr1:151081400-151089800	Weak transcription	Primary T helper cells PMA-I stimulated	--
45	chr1:151081400-151089800	Weak transcription	Fetal Brain Female	brain
46	chr1:151081400-151089800	Weak transcription	Rectal Mucosa Donor 29	rectum
47	chr1:151081400-151090000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
48	chr1:151081400-151103000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
49	chr1:151081600-151089800	Weak transcription	Stomach Smooth Muscle	stomach
50	chr1:151081600-151090200	Weak transcription	Brain Hippocampus Middle	brain

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