Variant report

Variant	rs2633608
Chromosome Location	chr3:112114155-112114156
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 50 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:31)

rs_ID	r²[population]
rs1386897	0.85[AFR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1586508	1.00[ASN][1000 genomes]
rs1872986	0.84[EUR][1000 genomes]
rs1872987	0.87[CEU][hapmap];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1996724	1.00[ASN][1000 genomes]
rs2029318	0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2087259	0.85[AFR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2129856	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2244035	1.00[ASN][1000 genomes]
rs2263365	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2633541	0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2633554	1.00[ASN][1000 genomes]
rs2633567	1.00[ASN][1000 genomes]
rs2633570	1.00[ASN][1000 genomes]
rs2633591	0.85[AFR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2633595	1.00[ASN][1000 genomes]
rs2633601	0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2633606	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2633607	1.00[AFR][1000 genomes];0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2683890	0.87[CEU][hapmap];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2683896	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2683897	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2683898	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2683901	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2683902	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2683903	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2683904	1.00[AFR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2931761	1.00[ASN][1000 genomes]
rs2971206	1.00[ASN][1000 genomes]
rs6799765	1.00[ASN][1000 genomes]
rs72952469	1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:19 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv877341	chr3:112079277-112125521	Strong transcription Flanking Active TSS Weak transcription Enhancers Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
2	nsv1002567	chr3:112088498-112144063	Weak transcription Enhancers Active TSS ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
3	esv2830128	chr3:112090292-112144026	Enhancers Active TSS Flanking Active TSS Weak transcription ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
4	nsv591294	chr3:112091220-112208750	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription Genic enhancers Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
5	nsv999904	chr3:112098217-112114816	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Strong transcription	Chromatin interactive region lncRNA	n/a	inside rSNPs	n/a
6	nsv1010208	chr3:112098542-112227212	Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Active TSS Genic enhancers Transcr. at gene 5' and 3' Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
7	nsv997659	chr3:112099148-112135687	Flanking Active TSS Enhancers Weak transcription Strong transcription ZNF genes & repeats Active TSS Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
8	nsv1006537	chr3:112099647-112114816	Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS Strong transcription Active TSS	Chromatin interactive region lncRNA	n/a	inside rSNPs	n/a
9	esv3494206	chr3:112101762-112115260	Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Active TSS Strong transcription	n/a	n/a	inside rSNPs	n/a
10	esv3494204	chr3:112102212-112115110	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS	n/a	n/a	inside rSNPs	n/a
11	nsv1003368	chr3:112102565-112114816	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS	n/a	n/a	inside rSNPs	n/a
12	nsv1008191	chr3:112102565-112114993	Enhancers Flanking Active TSS ZNF genes & repeats Weak transcription Active TSS	n/a	n/a	inside rSNPs	n/a
13	nsv998316	chr3:112102565-112116643	Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Active TSS	lncRNA	n/a	inside rSNPs	n/a
14	esv3463477	chr3:112102780-112114174	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS	n/a	n/a	inside rSNPs	n/a
15	esv3463478	chr3:112102780-112114174	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats	n/a	n/a	inside rSNPs	n/a
16	nsv516790	chr3:112103140-112114816	Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats Active TSS	n/a	n/a	inside rSNPs	n/a
17	nsv591299	chr3:112103140-112114816	Enhancers Flanking Active TSS ZNF genes & repeats Weak transcription Active TSS	n/a	n/a	inside rSNPs	n/a
18	nsv997722	chr3:112103509-112114816	Flanking Active TSS Weak transcription Enhancers Active TSS ZNF genes & repeats	n/a	n/a	inside rSNPs	n/a
19	nsv1011145	chr3:112103509-112114993	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats	n/a	n/a	inside rSNPs	n/a

No data

Chromatin state (count:49 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:112107200-112117000	Enhancers	Primary hematopoietic stem cells short term culture	blood
2	chr3:112107400-112117000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
3	chr3:112110400-112115200	Enhancers	Breast Myoepithelial Primary Cells	Breast
4	chr3:112110600-112114200	Weak transcription	Primary T helper cells PMA-I stimulated	--
5	chr3:112110600-112116600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
6	chr3:112110800-112114200	Weak transcription	Monocytes-CD14+_RO01746	blood
7	chr3:112110800-112118400	Weak transcription	Sigmoid Colon	Sigmoid Colon
8	chr3:112111000-112114400	Weak transcription	Rectal Mucosa Donor 29	rectum
9	chr3:112111400-112120400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
10	chr3:112111600-112114400	Weak transcription	Brain Angular Gyrus	brain
11	chr3:112111600-112114400	Weak transcription	Fetal Kidney	kidney
12	chr3:112111800-112125400	Weak transcription	Brain Inferior Temporal Lobe	brain
13	chr3:112112200-112114200	Weak transcription	Primary B cells from cord blood	blood
14	chr3:112112200-112116400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
15	chr3:112112400-112116600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
16	chr3:112112400-112118000	Weak transcription	H1 Cell Line	embryonic stem cell
17	chr3:112112600-112116400	Weak transcription	HUES64 Cell Line	embryonic stem cell
18	chr3:112112800-112116800	Enhancers	Fetal Lung	lung
19	chr3:112112800-112117000	Enhancers	Primary neutrophils fromperipheralblood	blood
20	chr3:112113000-112114600	Enhancers	iPS-18 Cell Line	embryonic stem cell
21	chr3:112113000-112114800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
22	chr3:112113000-112114800	Enhancers	Primary monocytes fromperipheralblood	blood
23	chr3:112113000-112115400	Enhancers	HUVEC	blood vessel
24	chr3:112113000-112115600	Enhancers	Fetal Muscle Leg	muscle
25	chr3:112113000-112116600	Weak transcription	HUES48 Cell Line	embryonic stem cell
26	chr3:112113200-112114600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
27	chr3:112113200-112114800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
28	chr3:112113200-112116400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
29	chr3:112113200-112117000	Enhancers	Placenta	Placenta
30	chr3:112113400-112114400	Weak transcription	Brain Cingulate Gyrus	brain
31	chr3:112113400-112115200	Enhancers	Adipose Nuclei	Adipose
32	chr3:112113400-112116400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
33	chr3:112113400-112116400	Weak transcription	HUES6 Cell Line	embryonic stem cell
34	chr3:112113400-112116600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
35	chr3:112113400-112117800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
36	chr3:112113400-112124600	Weak transcription	HMEC	breast
37	chr3:112113600-112114200	Weak transcription	Colon Smooth Muscle	Colon
38	chr3:112113600-112114400	Weak transcription	Fetal Stomach	stomach
39	chr3:112113600-112114600	Enhancers	Aorta	Aorta
40	chr3:112113600-112115200	Enhancers	Rectal Smooth Muscle	rectum
41	chr3:112113600-112116400	Weak transcription	Ovary	ovary
42	chr3:112113600-112116600	Weak transcription	H9 Cell Line	embryonic stem cell
43	chr3:112113600-112120600	Weak transcription	Rectal Mucosa Donor 31	rectum
44	chr3:112113800-112114800	Enhancers	Fetal Thymus	thymus
45	chr3:112114000-112114400	Flanking Active TSS	Primary hematopoietic stem cells	blood
46	chr3:112114000-112115000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
47	chr3:112114000-112115000	Enhancers	Primary T cells from cord blood	blood
48	chr3:112114000-112115400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
49	chr3:112114000-112116600	Weak transcription	Lung	lung

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