Variant report

Variant	rs7868374
Chromosome Location	chr9:21931609-21931610
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C9orf53-5	chr9:21930389-21932738	NONHSAT130406

Extended variants
information (count: 23 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:20)

rs_ID	r²[population]
rs10811639	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10965184	1.00[ASN][1000 genomes]
rs10965187	1.00[MEX][hapmap];0.81[AMR][1000 genomes]
rs11998828	1.00[ASN][1000 genomes]
rs12002708	1.00[ASN][1000 genomes]
rs12003027	0.93[GIH][hapmap];1.00[ASN][1000 genomes]
rs12003714	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2188126	0.86[GIH][hapmap]
rs2518714	1.00[YRI][hapmap];0.86[AFR][1000 genomes]
rs58869398	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73440481	1.00[ASN][1000 genomes]
rs73440484	1.00[ASN][1000 genomes]
rs73442446	1.00[ASN][1000 genomes]
rs73442448	0.89[AFR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73442453	1.00[ASN][1000 genomes]
rs73442470	1.00[ASN][1000 genomes]
rs73442472	1.00[ASN][1000 genomes]
rs73442474	1.00[ASN][1000 genomes]
rs7869195	0.81[AMR][1000 genomes]
rs7875199	0.86[GIH][hapmap]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv529609	chr9:21708371-22537069	Flanking Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription Bivalent/Poised TSS Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	35 gene(s)	inside rSNPs	diseases
2	nsv8426	chr9:21763810-22176200	Weak transcription Strong transcription Active TSS Enhancers ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	32 gene(s)	inside rSNPs	diseases
3	nsv892745	chr9:21857244-22006273	Bivalent Enhancer Enhancers Strong transcription ZNF genes & repeats Weak transcription Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	18 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:60 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:21911000-21935800	Weak transcription	HSMM	muscle
2	chr9:21919800-21932800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
3	chr9:21920600-21935000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
4	chr9:21920600-21942600	Weak transcription	Sigmoid Colon	Sigmoid Colon
5	chr9:21920800-21932000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
6	chr9:21921200-21934000	Weak transcription	H9 Cell Line	embryonic stem cell
7	chr9:21921200-21935600	Weak transcription	Primary T cells from cord blood	blood
8	chr9:21922200-21932400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
9	chr9:21922200-21933000	Weak transcription	H1 Cell Line	embryonic stem cell
10	chr9:21923800-21934000	Weak transcription	Thymus	Thymus
11	chr9:21923800-21934800	Weak transcription	Dnd41	blood
12	chr9:21924000-21934600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
13	chr9:21924800-21933000	Weak transcription	Lung	lung
14	chr9:21927000-21933400	Weak transcription	HSMMtube	muscle
15	chr9:21928000-21934800	Weak transcription	Psoas Muscle	Psoas
16	chr9:21928600-21931800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
17	chr9:21928600-21933200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
18	chr9:21928800-21933000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
19	chr9:21929200-21932600	Weak transcription	Duodenum Smooth Muscle	Duodenum
20	chr9:21929600-21932800	Weak transcription	Gastric	stomach
21	chr9:21929600-21933800	Weak transcription	Liver	Liver
22	chr9:21929800-21935600	Weak transcription	Stomach Smooth Muscle	stomach
23	chr9:21930000-21932000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
24	chr9:21930000-21932200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
25	chr9:21930000-21932600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
26	chr9:21930000-21932600	Weak transcription	Brain Cingulate Gyrus	brain
27	chr9:21930200-21932200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
28	chr9:21930200-21932600	Weak transcription	Spleen	Spleen
29	chr9:21930400-21932600	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
30	chr9:21930800-21932000	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
31	chr9:21930800-21932000	Strong transcription	Ovary	ovary
32	chr9:21930800-21933800	Weak transcription	Brain Inferior Temporal Lobe	brain
33	chr9:21931000-21931800	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
34	chr9:21931000-21931800	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Female	--
35	chr9:21931000-21931800	Genic enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
36	chr9:21931000-21931800	Enhancers	HMEC	breast
37	chr9:21931000-21932000	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
38	chr9:21931000-21932000	Enhancers	Muscle Satellite Cultured Cells	--
39	chr9:21931000-21932000	Strong transcription	Cortex derived primary cultured neurospheres	brain
40	chr9:21931000-21932000	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
41	chr9:21931000-21932000	Strong transcription	Aorta	Aorta
42	chr9:21931000-21932000	Strong transcription	Fetal Muscle Trunk	muscle
43	chr9:21931000-21932000	Strong transcription	Fetal Stomach	stomach
44	chr9:21931000-21932000	Strong transcription	Left Ventricle	heart
45	chr9:21931000-21932400	Strong transcription	Adipose Nuclei	Adipose
46	chr9:21931000-21933400	Weak transcription	Placenta	Placenta
47	chr9:21931200-21931800	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
48	chr9:21931200-21931800	ZNF genes & repeats	Breast Myoepithelial Primary Cells	Breast
49	chr9:21931200-21931800	Strong transcription	Primary hematopoietic stem cells	blood
50	chr9:21931200-21931800	Genic enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links