Variant report

Variant	rs4447144
Chromosome Location	chr11:102050321-102050322
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	chr11:102028899..102031250-chr11:102049975..102051895,2	K562	blood:

Extended variants
information (count: 54 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:45)

rs_ID	r²[population]
rs10750633	0.80[YRI][hapmap]
rs10895272	0.91[CEU][hapmap];0.82[CHB][hapmap];0.83[EUR][1000 genomes]
rs10895273	0.86[EUR][1000 genomes]
rs10895274	0.86[EUR][1000 genomes]
rs10895275	0.86[EUR][1000 genomes]
rs10895276	0.92[CEU][hapmap];0.86[EUR][1000 genomes]
rs10895277	0.91[CEU][hapmap];0.82[CHB][hapmap];0.86[EUR][1000 genomes]
rs10895278	0.92[CEU][hapmap];0.82[CHB][hapmap];0.83[EUR][1000 genomes]
rs11225156	0.96[CEU][hapmap];0.90[CHB][hapmap];1.00[JPT][hapmap];0.95[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs11225160	1.00[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.82[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11225163	1.00[CEU][hapmap];0.92[EUR][1000 genomes]
rs11225165	0.86[EUR][1000 genomes]
rs11225167	0.87[EUR][1000 genomes]
rs11225170	0.86[CEU][hapmap];0.82[CHB][hapmap];0.82[EUR][1000 genomes]
rs11225174	0.92[CEU][hapmap];0.82[CHB][hapmap];0.83[EUR][1000 genomes]
rs11605954	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.80[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11608234	0.81[EUR][1000 genomes]
rs12223991	0.82[EUR][1000 genomes]
rs12226331	1.00[CEU][hapmap];0.91[EUR][1000 genomes]
rs12420287	0.94[EUR][1000 genomes]
rs12421242	0.93[EUR][1000 genomes]
rs12786272	0.86[EUR][1000 genomes]
rs12787996	0.96[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.86[AMR][1000 genomes];0.93[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12790399	0.83[EUR][1000 genomes]
rs12793501	0.83[AMR][1000 genomes];0.93[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12795624	1.00[CEU][hapmap];0.90[EUR][1000 genomes]
rs17097547	0.92[CEU][hapmap];0.82[CHB][hapmap];0.84[EUR][1000 genomes]
rs17097560	0.92[CEU][hapmap];0.82[CHB][hapmap];0.84[EUR][1000 genomes]
rs1820455	0.86[EUR][1000 genomes]
rs1834596	0.81[YRI][hapmap]
rs1893498	1.00[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.86[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2187525	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.99[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2282652	0.91[CEU][hapmap];0.82[CHB][hapmap];0.83[EUR][1000 genomes]
rs3858420	0.91[CEU][hapmap];0.83[EUR][1000 genomes]
rs4475891	0.91[CEU][hapmap];0.83[EUR][1000 genomes]
rs4754041	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs57027482	0.81[EUR][1000 genomes]
rs58751289	0.83[EUR][1000 genomes]
rs7110557	1.00[CEU][hapmap];0.92[EUR][1000 genomes]
rs7120067	0.95[CEU][hapmap];0.88[EUR][1000 genomes]
rs7122907	0.91[CEU][hapmap];0.82[CHB][hapmap];0.87[EUR][1000 genomes]
rs7124247	0.83[EUR][1000 genomes]
rs7931576	0.92[CEU][hapmap];0.84[EUR][1000 genomes]
rs7942061	0.86[EUR][1000 genomes]
rs8504	0.91[CEU][hapmap];0.83[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:9 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3362945	chr11:101736547-102114246	Flanking Active TSS Weak transcription Enhancers Strong transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	13 gene(s)	inside rSNPs	diseases
2	nsv898333	chr11:101832670-102079986	Active TSS Flanking Bivalent TSS/Enh Enhancers Weak transcription Strong transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
3	nsv1052348	chr11:101987090-102255753	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Active TSS Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	11 gene(s)	inside rSNPs	diseases
4	nsv556141	chr11:101988061-102207851	Weak transcription Genic enhancers Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
5	nsv1050961	chr11:101993880-102253717	Weak transcription Strong transcription Enhancers Flanking Active TSS Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	11 gene(s)	inside rSNPs	diseases
6	nsv1051735	chr11:101993880-102255753	Weak transcription Active TSS Strong transcription Flanking Active TSS Enhancers Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	11 gene(s)	inside rSNPs	diseases
7	nsv530646	chr11:102000840-102238992	Enhancers Strong transcription Flanking Active TSS Weak transcription Genic enhancers Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	11 gene(s)	inside rSNPs	diseases
8	nsv832251	chr11:102012295-102181744	Weak transcription Enhancers Strong transcription Active TSS Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
9	nsv1043388	chr11:102017719-102172857	Genic enhancers Enhancers Flanking Active TSS Active TSS Strong transcription Bivalent/Poised TSS Weak transcription Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region miRNA target site	8 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:80 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:102026400-102059400	Weak transcription	Fetal Brain Male	brain
2	chr11:102028000-102062800	Weak transcription	Duodenum Mucosa	Duodenum
3	chr11:102028600-102055200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
4	chr11:102029200-102067600	Weak transcription	HSMMtube	muscle
5	chr11:102033400-102061000	Weak transcription	Right Ventricle	heart
6	chr11:102034400-102055200	Weak transcription	Cortex derived primary cultured neurospheres	brain
7	chr11:102034400-102057200	Weak transcription	H1 Cell Line	embryonic stem cell
8	chr11:102034600-102076800	Weak transcription	Rectal Mucosa Donor 29	rectum
9	chr11:102035400-102055600	Weak transcription	Rectal Mucosa Donor 31	rectum
10	chr11:102036000-102069400	Weak transcription	Sigmoid Colon	Sigmoid Colon
11	chr11:102039600-102056800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
12	chr11:102041600-102062400	Weak transcription	Left Ventricle	heart
13	chr11:102042400-102055400	Weak transcription	Colon Smooth Muscle	Colon
14	chr11:102042800-102057200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
15	chr11:102043800-102051600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
16	chr11:102043800-102077000	Weak transcription	Esophagus	oesophagus
17	chr11:102043800-102100400	Weak transcription	Pancreas	Pancrea
18	chr11:102044000-102055200	Weak transcription	Gastric	stomach
19	chr11:102045800-102050800	Weak transcription	Fetal Muscle Trunk	muscle
20	chr11:102046000-102055400	Weak transcription	Ovary	ovary
21	chr11:102046600-102056800	Weak transcription	HUES6 Cell Line	embryonic stem cell
22	chr11:102046600-102057000	Weak transcription	Fetal Kidney	kidney
23	chr11:102046800-102056800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
24	chr11:102046800-102076600	Weak transcription	Stomach Smooth Muscle	stomach
25	chr11:102047000-102057200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
26	chr11:102047600-102050400	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
27	chr11:102047600-102050600	Enhancers	HMEC	breast
28	chr11:102047800-102050400	Enhancers	HUVEC	blood vessel
29	chr11:102048000-102055200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
30	chr11:102048200-102050400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
31	chr11:102048200-102062400	Weak transcription	Liver	Liver
32	chr11:102048400-102065200	Weak transcription	Aorta	Aorta
33	chr11:102048400-102073600	Weak transcription	Psoas Muscle	Psoas
34	chr11:102048400-102077200	Weak transcription	Lung	lung
35	chr11:102048600-102051800	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
36	chr11:102048800-102051200	ZNF genes & repeats	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
37	chr11:102049000-102051800	Strong transcription	HUES64 Cell Line	embryonic stem cell
38	chr11:102049200-102050400	Genic enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
39	chr11:102049200-102050800	Genic enhancers	A549	lung
40	chr11:102049200-102051000	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
41	chr11:102049200-102051200	Strong transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
42	chr11:102049200-102055200	Weak transcription	Skeletal Muscle Female	skeletal muscle
43	chr11:102049200-102056800	Weak transcription	HUES48 Cell Line	embryonic stem cell
44	chr11:102049200-102056800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
45	chr11:102049400-102050400	Genic enhancers	Placenta	Placenta
46	chr11:102049400-102050600	Genic enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
47	chr11:102049400-102051800	ZNF genes & repeats	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
48	chr11:102049400-102051800	Strong transcription	Breast Myoepithelial Primary Cells	Breast
49	chr11:102049400-102052000	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
50	chr11:102049600-102051000	Genic enhancers	NHEK	skin

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