Variant report

Variant	rs6671703
Chromosome Location	chr1:150796970-150796971
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr1:150794318..150797920-chr1:150799391..150802153,4	MCF-7	breast:
2	chr1:150788842..150790398-chr1:150796829..150799047,2	K562	blood:

Extended variants
information (count: 38 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:30)

rs_ID	r²[population]
rs10788795	0.88[EUR][1000 genomes]
rs10888396	0.92[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs11204714	0.85[EUR][1000 genomes]
rs11204715	0.85[EUR][1000 genomes]
rs11204727	0.88[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs11576175	0.88[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs12728254	0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs16840074	0.82[EUR][1000 genomes]
rs1811698	0.83[ASN][1000 genomes]
rs2134688	0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs3738483	0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs3768017	0.93[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3820541	0.93[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs3820543	0.93[AMR][1000 genomes];0.96[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4379678	0.93[AMR][1000 genomes];0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs533928	0.85[EUR][1000 genomes]
rs61817598	0.82[EUR][1000 genomes]
rs61817600	0.88[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs61817649	0.85[EUR][1000 genomes]
rs6661100	0.88[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs6679701	0.88[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs6684611	0.83[ASN][1000 genomes]
rs6688248	0.85[EUR][1000 genomes]
rs6692277	0.88[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs6696167	0.88[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs72704624	0.88[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs7517566	0.93[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7529204	0.93[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7535848	0.85[EUR][1000 genomes]
rs7535975	0.85[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2829859	chr1:150608894-150937329	Flanking Active TSS Weak transcription Enhancers Strong transcription Active TSS Genic enhancers 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	38 gene(s)	inside rSNPs	diseases
2	nsv872418	chr1:150683512-150860471	Enhancers Strong transcription Weak transcription Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	28 gene(s)	inside rSNPs	diseases
3	nsv437169	chr1:150738197-150816886	Enhancers Strong transcription Weak transcription Flanking Active TSS Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
4	nsv1001897	chr1:150743271-151241600	Flanking Active TSS Enhancers Weak transcription Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	156 gene(s)	inside rSNPs	diseases
5	nsv535158	chr1:150743271-151241600	Genic enhancers Weak transcription Strong transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	156 gene(s)	inside rSNPs	diseases
6	nsv2788	chr1:150755334-150800785	Weak transcription Strong transcription Enhancers Active TSS Flanking Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
7	nsv872420	chr1:150786038-150847647	Strong transcription Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats Genic enhancers Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
8	nsv1010875	chr1:150796816-150845827	Weak transcription Strong transcription ZNF genes & repeats Enhancers Flanking Active TSS Genic enhancers Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	11 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:125 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:150782200-150809600	Strong transcription	Fetal Muscle Leg	muscle
2	chr1:150782200-150809800	Strong transcription	Stomach Smooth Muscle	stomach
3	chr1:150782200-150813000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
4	chr1:150782400-150812200	Strong transcription	Primary T cells fromperipheralblood	blood
5	chr1:150782600-150802800	Strong transcription	Primary T helper cells fromperipheralblood	blood
6	chr1:150783000-150797000	Strong transcription	HUES64 Cell Line	embryonic stem cell
7	chr1:150783200-150797000	Strong transcription	HUES6 Cell Line	embryonic stem cell
8	chr1:150783200-150809800	Strong transcription	Fetal Thymus	thymus
9	chr1:150783200-150816600	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
10	chr1:150783200-150816800	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
11	chr1:150784000-150802000	Strong transcription	Fetal Lung	lung
12	chr1:150785800-150806400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
13	chr1:150785800-150812400	Strong transcription	Primary neutrophils fromperipheralblood	blood
14	chr1:150786000-150808600	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
15	chr1:150788400-150808000	Strong transcription	Rectal Mucosa Donor 31	rectum
16	chr1:150788400-150809800	Strong transcription	Fetal Muscle Trunk	muscle
17	chr1:150788400-150812200	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
18	chr1:150788800-150797200	Strong transcription	HUVEC	blood vessel
19	chr1:150789400-150801000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
20	chr1:150789600-150798000	Weak transcription	Stomach Mucosa	stomach
21	chr1:150789600-150801000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
22	chr1:150789800-150798800	Weak transcription	A549	lung
23	chr1:150790000-150799800	Weak transcription	H1 Cell Line	embryonic stem cell
24	chr1:150790000-150801400	Weak transcription	Fetal Brain Male	brain
25	chr1:150790000-150804600	Weak transcription	Pancreas	Pancrea
26	chr1:150790600-150798200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
27	chr1:150790600-150801000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
28	chr1:150790600-150802400	Weak transcription	Esophagus	oesophagus
29	chr1:150790800-150811400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
30	chr1:150791200-150806600	Weak transcription	Small Intestine	intestine
31	chr1:150791800-150809000	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
32	chr1:150792200-150814800	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
33	chr1:150792400-150801800	Strong transcription	Colon Smooth Muscle	Colon
34	chr1:150792600-150803200	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
35	chr1:150792600-150815400	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
36	chr1:150792800-150812400	Strong transcription	Primary B cells from peripheral blood	blood
37	chr1:150793000-150799000	Strong transcription	Primary T helper naive cells from peripheral blood	blood
38	chr1:150793000-150816400	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
39	chr1:150793200-150823200	Strong transcription	Placenta	Placenta
40	chr1:150793600-150815800	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
41	chr1:150793800-150813800	Strong transcription	Primary monocytes fromperipheralblood	blood
42	chr1:150794000-150797400	Weak transcription	HSMM	muscle
43	chr1:150794000-150797800	Weak transcription	HMEC	breast
44	chr1:150794000-150798600	Strong transcription	Liver	Liver
45	chr1:150794000-150800000	Strong transcription	Fetal Stomach	stomach
46	chr1:150794000-150800800	Weak transcription	K562	blood
47	chr1:150794000-150805800	Strong transcription	Osteobl	bone
48	chr1:150794000-150809600	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
49	chr1:150794000-150813600	Strong transcription	Monocytes-CD14+_RO01746	blood
50	chr1:150794200-150798600	Weak transcription	NHEK	skin

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