Variant report

Variant	rs10874941
Chromosome Location	chr1:92242760-92242761
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	chr1:92237802..92240400-chr1:92241191..92243565,2	K562	blood:

Extended variants
information (count: 51 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs10874940	0.89[CHB][hapmap]
rs10874976	0.89[CHB][hapmap]
rs11165489	0.89[CHB][hapmap]
rs11165496	0.80[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs11165532	0.94[CHB][hapmap]
rs11466573	0.87[ASN][1000 genomes]
rs1192530	0.92[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs12090296	0.89[CHB][hapmap]
rs12756024	0.96[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1411276	0.89[CHB][hapmap]
rs1473486	0.92[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.91[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1473488	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.92[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1473767	0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2171584	0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2297142	0.93[CHB][hapmap]
rs2391068	0.89[CHB][hapmap]
rs2391069	0.89[CHB][hapmap]
rs4658113	0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4658268	0.82[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs5019497	1.00[CHB][hapmap];0.86[JPT][hapmap];0.86[ASN][1000 genomes]
rs6604054	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6604055	0.96[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6604056	1.00[CHB][hapmap];0.86[JPT][hapmap];0.87[ASN][1000 genomes]
rs6669044	0.89[CHB][hapmap]
rs6678564	0.93[CHB][hapmap]
rs6683840	0.96[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs6691098	0.89[CHB][hapmap]
rs7521065	0.82[CHB][hapmap]
rs7530883	0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7534318	0.89[CHB][hapmap]
rs7536947	0.89[CHB][hapmap]

Variant overlapped rSNPs/rCNVs (count:20 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1009560	chr1:91897078-92270781	Enhancers Strong transcription Bivalent Enhancer Weak transcription Flanking Active TSS Genic enhancers Active TSS ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	14 gene(s)	inside rSNPs	diseases
2	nsv1012864	chr1:92067100-92827761	Flanking Active TSS Strong transcription Enhancers Active TSS Weak transcription Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	33 gene(s)	inside rSNPs	diseases
3	nsv535029	chr1:92067100-92827761	Strong transcription Weak transcription Enhancers Active TSS Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	33 gene(s)	inside rSNPs	diseases
4	nsv530438	chr1:92091957-92827760	Weak transcription Active TSS Strong transcription Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	33 gene(s)	inside rSNPs	diseases
5	nsv1010179	chr1:92140209-92655952	Weak transcription Genic enhancers Flanking Active TSS Enhancers Strong transcription Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	19 gene(s)	inside rSNPs	diseases
6	nsv535030	chr1:92140209-92655952	Enhancers Weak transcription Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Strong transcription ZNF genes & repeats Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	19 gene(s)	inside rSNPs	diseases
7	nsv1005917	chr1:92189945-92378683	Flanking Active TSS Enhancers Weak transcription Genic enhancers Strong transcription Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
8	nsv949449	chr1:92211020-92585831	Strong transcription Enhancers Genic enhancers Weak transcription Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
9	nsv524845	chr1:92215725-92598705	Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
10	nsv462517	chr1:92215725-92598705	Weak transcription Bivalent Enhancer Enhancers Active TSS Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
11	nsv546810	chr1:92215725-92598705	Flanking Active TSS Enhancers Weak transcription Active TSS Genic enhancers Strong transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
12	nsv1006318	chr1:92216408-92608324	Flanking Active TSS Enhancers Active TSS Transcr. at gene 5' and 3' Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Strong transcription ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
13	nsv432498	chr1:92218245-92618323	Weak transcription Strong transcription Genic enhancers Flanking Active TSS Enhancers Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
14	nsv1004570	chr1:92220544-92622129	Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
15	nsv1007661	chr1:92220544-92655952	Weak transcription Enhancers Active TSS Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases
16	nsv1014837	chr1:92233905-92618839	Enhancers Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
17	nsv535031	chr1:92233905-92618839	Bivalent/Poised TSS Enhancers Weak transcription Bivalent Enhancer Genic enhancers Strong transcription Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
18	nsv1012134	chr1:92235485-92598800	Weak transcription Genic enhancers Flanking Active TSS Active TSS Enhancers Strong transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
19	nsv546818	chr1:92236048-92579206	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
20	nsv519291	chr1:92240685-92248695	Weak transcription Enhancers Genic enhancers Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:69 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:92204800-92247000	Weak transcription	Primary T helper cells fromperipheralblood	blood
2	chr1:92217800-92247800	Weak transcription	Small Intestine	intestine
3	chr1:92220600-92255800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
4	chr1:92221000-92248000	Weak transcription	Primary T helper cells PMA-I stimulated	--
5	chr1:92224400-92242800	Weak transcription	Pancreatic Islets	Pancreatic Islet
6	chr1:92227000-92257200	Weak transcription	Fetal Intestine Small	intestine
7	chr1:92230600-92247800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
8	chr1:92231000-92246800	Weak transcription	Hela-S3	cervix
9	chr1:92232600-92243200	Weak transcription	H1 Cell Line	embryonic stem cell
10	chr1:92233200-92257000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
11	chr1:92233400-92246800	Weak transcription	A549	lung
12	chr1:92235600-92243200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
13	chr1:92235600-92243600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
14	chr1:92235600-92244600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
15	chr1:92235600-92247800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
16	chr1:92235800-92244600	Weak transcription	Right Ventricle	heart
17	chr1:92235800-92246600	Weak transcription	K562	blood
18	chr1:92236000-92243400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
19	chr1:92236400-92246000	Weak transcription	NHLF	lung
20	chr1:92236600-92243000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
21	chr1:92236800-92242800	Weak transcription	Duodenum Smooth Muscle	Duodenum
22	chr1:92236800-92243400	Weak transcription	Fetal Kidney	kidney
23	chr1:92237400-92243800	Enhancers	Breast Myoepithelial Primary Cells	Breast
24	chr1:92238600-92249400	Genic enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
25	chr1:92238800-92245000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
26	chr1:92239200-92246600	Weak transcription	Primary T cells fromperipheralblood	blood
27	chr1:92240000-92243800	Enhancers	Liver	Liver
28	chr1:92240200-92243400	Enhancers	Pancreas	Pancrea
29	chr1:92240200-92243600	Enhancers	Ovary	ovary
30	chr1:92240200-92243600	Enhancers	Stomach Smooth Muscle	stomach
31	chr1:92240600-92243200	Genic enhancers	NHDF-Ad	bronchial
32	chr1:92240800-92242800	Genic enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
33	chr1:92240800-92243200	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
34	chr1:92240800-92246400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
35	chr1:92241000-92246400	Weak transcription	Osteobl	bone
36	chr1:92241200-92244400	Weak transcription	Placenta	Placenta
37	chr1:92241200-92244600	Weak transcription	Brain Cingulate Gyrus	brain
38	chr1:92241200-92249000	Strong transcription	HepG2	liver
39	chr1:92241400-92243400	Enhancers	Right Atrium	heart
40	chr1:92241400-92246400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
41	chr1:92241400-92255800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
42	chr1:92241600-92242800	Enhancers	Skeletal Muscle Male	skeletal muscle
43	chr1:92241600-92243400	Enhancers	Esophagus	oesophagus
44	chr1:92241600-92243800	Enhancers	Fetal Muscle Leg	muscle
45	chr1:92241800-92243400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
46	chr1:92241800-92243400	Enhancers	Skeletal Muscle Female	skeletal muscle
47	chr1:92241800-92248000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
48	chr1:92241800-92255800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
49	chr1:92242000-92244400	Weak transcription	HUES48 Cell Line	embryonic stem cell
50	chr1:92242000-92244400	Weak transcription	Fetal Muscle Trunk	muscle

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links