Variant report

Variant	rs4544710
Chromosome Location	chr4:6999570-6999571
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	chr4:6997053..6999861-chr4:7067007..7069346,2	K562	blood:

Variant related genes	Relation type
ENSG00000109519	Chromatin interaction

Extended variants
information (count: 88 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:83)

rs_ID	r²[population]
rs10012590	0.87[CEU][hapmap];1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs10025310	0.83[CEU][hapmap];1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs10516181	0.81[ASN][1000 genomes]
rs10937774	1.00[CHB][hapmap]
rs10937776	0.81[ASN][1000 genomes]
rs11732898	1.00[CHB][hapmap];0.81[ASN][1000 genomes]
rs11938701	1.00[ASN][1000 genomes]
rs11944897	1.00[ASN][1000 genomes]
rs12502513	1.00[CHB][hapmap];0.81[ASN][1000 genomes]
rs12503027	1.00[ASN][1000 genomes]
rs12510715	0.81[ASN][1000 genomes]
rs12512484	0.84[EUR][1000 genomes]
rs13107989	1.00[ASN][1000 genomes]
rs13108082	0.86[ASN][1000 genomes]
rs13111887	0.86[ASN][1000 genomes]
rs13122119	1.00[CHB][hapmap];0.93[ASN][1000 genomes]
rs13148395	0.81[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13149411	0.87[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs13149923	0.87[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs2301817	1.00[CHB][hapmap];0.83[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs2301818	0.94[CEU][hapmap];0.81[AMR][1000 genomes];0.97[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2301819	0.85[AMR][1000 genomes];0.83[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2359194	0.81[ASN][1000 genomes]
rs3188939	0.87[CEU][hapmap];1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs34219101	0.86[ASN][1000 genomes]
rs34221933	0.86[AFR][1000 genomes];0.95[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34335938	0.81[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs34379427	0.84[EUR][1000 genomes]
rs34463709	0.93[ASN][1000 genomes]
rs34481892	0.93[ASN][1000 genomes]
rs34953654	0.81[ASN][1000 genomes]
rs34959511	0.93[ASN][1000 genomes]
rs34990775	0.87[EUR][1000 genomes]
rs35170004	0.93[ASN][1000 genomes]
rs35680216	0.84[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs3857171	0.81[ASN][1000 genomes]
rs3892490	1.00[CHB][hapmap];0.86[ASN][1000 genomes]
rs3894945	1.00[ASN][1000 genomes]
rs4234788	0.86[ASN][1000 genomes]
rs4234791	1.00[CHB][hapmap];0.93[ASN][1000 genomes]
rs4234793	1.00[ASN][1000 genomes]
rs4376137	0.81[YRI][hapmap]
rs4423873	0.93[YRI][hapmap]
rs4689056	0.87[EUR][1000 genomes]
rs4689560	0.83[CEU][hapmap];1.00[CHB][hapmap];0.84[EUR][1000 genomes]
rs4689563	0.93[ASN][1000 genomes]
rs4689564	0.93[ASN][1000 genomes]
rs4689565	0.83[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs4689566	0.81[ASN][1000 genomes]
rs4689567	0.81[ASN][1000 genomes]
rs4689568	1.00[CHB][hapmap];0.81[ASN][1000 genomes]
rs4689573	0.81[ASN][1000 genomes]
rs4689575	0.86[CEU][hapmap];1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs4689577	0.81[ASN][1000 genomes]
rs4689579	0.93[ASN][1000 genomes]
rs55822670	0.86[ASN][1000 genomes]
rs62289166	1.00[ASN][1000 genomes]
rs6446559	0.86[ASN][1000 genomes]
rs66530709	0.93[ASN][1000 genomes]
rs66640699	0.93[ASN][1000 genomes]
rs66841627	0.87[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs66931928	0.93[ASN][1000 genomes]
rs66992702	0.93[ASN][1000 genomes]
rs6811496	1.00[ASN][1000 genomes]
rs6816660	0.86[ASN][1000 genomes]
rs6816882	0.86[ASN][1000 genomes]
rs6818744	0.87[CEU][hapmap];1.00[CHB][hapmap];0.93[ASN][1000 genomes]
rs6831129	0.86[ASN][1000 genomes]
rs6834102	1.00[ASN][1000 genomes]
rs6835187	0.87[YRI][hapmap]
rs6840780	0.86[AFR][1000 genomes];0.95[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6854776	0.87[CEU][hapmap];1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs7655563	1.00[CHB][hapmap];0.81[ASN][1000 genomes]
rs7655773	0.93[CEU][hapmap];1.00[CHB][hapmap];0.85[YRI][hapmap];0.86[AFR][1000 genomes];0.95[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7658198	1.00[CHB][hapmap];0.86[ASN][1000 genomes]
rs7661462	1.00[CHB][hapmap];0.86[ASN][1000 genomes]
rs7661952	1.00[CEU][hapmap];1.00[CHB][hapmap];0.87[YRI][hapmap];0.86[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7673901	1.00[ASN][1000 genomes]
rs7675524	1.00[CHB][hapmap];0.81[YRI][hapmap];0.81[ASN][1000 genomes]
rs7685667	1.00[ASN][1000 genomes]
rs7689324	0.81[YRI][hapmap]
rs7693321	0.81[ASN][1000 genomes]
rs9291126	0.93[YRI][hapmap];0.84[AFR][1000 genomes];0.86[ASN][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	nsv878530	chr4:6888932-7058473	Strong transcription Enhancers Weak transcription Genic enhancers Bivalent Enhancer Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	39 gene(s)	inside rSNPs	diseases
2	esv34033	chr4:6973270-7390621	Weak transcription Enhancers Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	40 gene(s)	inside rSNPs	diseases
3	esv2757919	chr4:6988148-7269901	Genic enhancers Strong transcription Flanking Active TSS Bivalent Enhancer Weak transcription Enhancers Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	38 gene(s)	inside rSNPs	diseases
4	esv2759221	chr4:6988148-7269901	Active TSS Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	38 gene(s)	inside rSNPs	diseases
5	nsv428436	chr4:6988148-7269901	Bivalent Enhancer Weak transcription Bivalent/Poised TSS Active TSS Enhancers Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	38 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:126 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:6990400-7008800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr4:6991000-7021800	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr4:6991400-7000800	Weak transcription	Colonic Mucosa	Colon
4	chr4:6991600-7000000	Weak transcription	Hela-S3	cervix
5	chr4:6993200-7006800	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
6	chr4:6993800-7008400	Strong transcription	iPS-20b Cell Line	embryonic stem cell
7	chr4:6994000-7000200	Weak transcription	Primary hematopoietic stem cells	blood
8	chr4:6994000-7005200	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
9	chr4:6994000-7008600	Strong transcription	HUES6 Cell Line	embryonic stem cell
10	chr4:6994000-7035600	Strong transcription	Fetal Stomach	stomach
11	chr4:6994000-7043200	Weak transcription	Right Atrium	heart
12	chr4:6994200-7000400	Weak transcription	Fetal Heart	heart
13	chr4:6994200-7000600	Strong transcription	Fetal Muscle Leg	muscle
14	chr4:6994200-7035400	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
15	chr4:6994400-6999600	Strong transcription	Primary neutrophils fromperipheralblood	blood
16	chr4:6994400-7000800	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
17	chr4:6994400-7000800	Weak transcription	Pancreas	Pancrea
18	chr4:6994400-7001000	Strong transcription	Fetal Muscle Trunk	muscle
19	chr4:6994400-7013400	Strong transcription	Primary hematopoietic stem cells short term culture	blood
20	chr4:6994600-6999600	Strong transcription	Primary T cells from cord blood	blood
21	chr4:6994600-6999600	Strong transcription	Monocytes-CD14+_RO01746	blood
22	chr4:6994600-7000200	Strong transcription	Primary T cells fromperipheralblood	blood
23	chr4:6994600-7006800	Strong transcription	Stomach Smooth Muscle	stomach
24	chr4:6994600-7021400	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
25	chr4:6994800-6999800	Strong transcription	Primary T helper cells PMA-I stimulated	--
26	chr4:6994800-7000600	Strong transcription	Primary T helper cells fromperipheralblood	blood
27	chr4:6994800-7007600	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
28	chr4:6995000-7009200	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
29	chr4:6995000-7020800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
30	chr4:6995200-6999800	Strong transcription	Placenta	Placenta
31	chr4:6995200-7000200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
32	chr4:6995200-7000600	Weak transcription	Brain Substantia Nigra	brain
33	chr4:6995200-7000600	Weak transcription	Pancreatic Islets	Pancreatic Islet
34	chr4:6995200-7000800	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
35	chr4:6995200-7008400	Strong transcription	HUES48 Cell Line	embryonic stem cell
36	chr4:6995200-7008600	Strong transcription	Fetal Intestine Small	intestine
37	chr4:6995400-6999800	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
38	chr4:6995400-6999800	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
39	chr4:6995400-7000800	Weak transcription	Brain Angular Gyrus	brain
40	chr4:6995400-7005000	Strong transcription	GM12878-XiMat	blood
41	chr4:6995400-7006600	Strong transcription	Duodenum Mucosa	Duodenum
42	chr4:6995400-7007800	Strong transcription	iPS-18 Cell Line	embryonic stem cell
43	chr4:6995400-7008600	Strong transcription	Fetal Intestine Large	intestine
44	chr4:6995400-7013600	Strong transcription	Fetal Thymus	thymus
45	chr4:6995600-7006800	Strong transcription	Rectal Mucosa Donor 29	rectum
46	chr4:6995800-7000600	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
47	chr4:6995800-7001600	Strong transcription	Liver	Liver
48	chr4:6995800-7003400	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
49	chr4:6995800-7004200	Strong transcription	Breast Myoepithelial Primary Cells	Breast
50	chr4:6995800-7006800	Strong transcription	H1 Cell Line	embryonic stem cell

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