Variant report

Variant	rs11809441
Chromosome Location	chr1:212305750-212305751
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr1:212305625..212307836-chr1:212314959..212318281,3	K562	blood:
2	chr1:212280661..212282639-chr1:212303880..212306262,2	K562	blood:

Extended variants
information (count: 14 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:12)

rs_ID	r²[population]
rs11579154	0.88[YRI][hapmap]
rs11802189	0.87[AFR][1000 genomes]
rs56810476	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs57901353	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs58525076	0.97[AFR][1000 genomes]
rs73091223	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73091229	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73091246	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73091249	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73091261	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73091264	0.87[AFR][1000 genomes]
rs7528369	0.82[YRI][hapmap]

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	nsv999738	chr1:212218618-212513690	Enhancers Weak transcription Strong transcription Active TSS ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	36 gene(s)	inside rSNPs	diseases
2	nsv1009376	chr1:212292357-212680320	Weak transcription Strong transcription Enhancers Transcr. at gene 5' and 3' Active TSS ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	48 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:32 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:212274400-212308200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr1:212281200-212308400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
3	chr1:212285600-212311200	Weak transcription	Hela-S3	cervix
4	chr1:212287400-212320600	Weak transcription	A549	lung
5	chr1:212292600-212314600	Weak transcription	Thymus	Thymus
6	chr1:212293200-212313200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
7	chr1:212298200-212307200	Strong transcription	Dnd41	blood
8	chr1:212298600-212306200	Weak transcription	H9 Cell Line	embryonic stem cell
9	chr1:212298600-212312200	Weak transcription	Gastric	stomach
10	chr1:212298800-212308200	Weak transcription	Fetal Muscle Trunk	muscle
11	chr1:212299000-212308000	Weak transcription	Primary hematopoietic stem cells	blood
12	chr1:212299000-212313000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
13	chr1:212299200-212307800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
14	chr1:212299200-212314200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
15	chr1:212299800-212308600	Weak transcription	Monocytes-CD14+_RO01746	blood
16	chr1:212300000-212308400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
17	chr1:212300000-212320800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
18	chr1:212300800-212306200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
19	chr1:212300800-212314800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
20	chr1:212301000-212308000	Weak transcription	Cortex derived primary cultured neurospheres	brain
21	chr1:212301000-212321000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
22	chr1:212302800-212307400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
23	chr1:212303600-212306600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
24	chr1:212303800-212305800	Strong transcription	K562	blood
25	chr1:212304000-212316400	Weak transcription	Fetal Stomach	stomach
26	chr1:212305000-212305800	Strong transcription	Primary hematopoietic stem cells short term culture	blood
27	chr1:212305000-212305800	Enhancers	HepG2	liver
28	chr1:212305000-212306000	Enhancers	Fetal Intestine Small	intestine
29	chr1:212305200-212305800	Enhancers	NHDF-Ad	bronchial
30	chr1:212305200-212306200	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
31	chr1:212305600-212305800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
32	chr1:212305600-212306000	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin

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