Variant report

Variant	rs981460
Chromosome Location	chr1:171191583-171191584
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 14 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:8)

rs_ID	r²[population]
rs10798271	0.83[CEU][hapmap];1.00[CHB][hapmap];0.93[CHD][hapmap];0.95[JPT][hapmap];0.96[ASN][1000 genomes]
rs10912593	0.83[CEU][hapmap];1.00[CHB][hapmap];0.95[CHD][hapmap];0.95[JPT][hapmap];0.96[ASN][1000 genomes]
rs12061191	0.95[ASN][1000 genomes]
rs12078610	0.84[ASN][1000 genomes]
rs16864216	0.82[YRI][hapmap]
rs28369847	0.89[EUR][1000 genomes]
rs7535566	0.96[ASN][1000 genomes]
rs7535771	0.96[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1001228	chr1:170885787-171452579	Enhancers Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	23 gene(s)	inside rSNPs	diseases
2	esv14617	chr1:171016086-171726961	Enhancers Weak transcription Flanking Active TSS Strong transcription Genic enhancers Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	52 gene(s)	inside rSNPs	diseases
3	nsv1005902	chr1:171036690-171254916	Enhancers Active TSS Weak transcription Flanking Active TSS Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	14 gene(s)	inside rSNPs	diseases
4	nsv535203	chr1:171036690-171254916	Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	14 gene(s)	inside rSNPs	diseases
5	esv10193	chr1:171128845-171414611	Weak transcription Active TSS Enhancers Bivalent Enhancer Flanking Active TSS Strong transcription ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
6	nsv831882	chr1:171166224-171326083	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:59 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:171188000-171192200	Weak transcription	Pancreas	Pancrea
2	chr1:171189000-171191600	Weak transcription	Small Intestine	intestine
3	chr1:171189200-171192600	Enhancers	Muscle Satellite Cultured Cells	--
4	chr1:171189800-171193400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
5	chr1:171190000-171192400	Enhancers	Osteobl	bone
6	chr1:171190000-171192600	Enhancers	HMEC	breast
7	chr1:171190200-171192000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
8	chr1:171190200-171192200	Weak transcription	Brain Cingulate Gyrus	brain
9	chr1:171190200-171192200	Weak transcription	Rectal Smooth Muscle	rectum
10	chr1:171190200-171192400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
11	chr1:171190200-171192400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
12	chr1:171190200-171192600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
13	chr1:171190200-171192600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
14	chr1:171190200-171192600	Enhancers	Fetal Muscle Leg	muscle
15	chr1:171190200-171192600	Enhancers	NHLF	lung
16	chr1:171190200-171192800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
17	chr1:171190200-171193200	Enhancers	Cortex derived primary cultured neurospheres	brain
18	chr1:171190200-171193400	Enhancers	NHEK	skin
19	chr1:171190200-171193800	Enhancers	Fetal Lung	lung
20	chr1:171190400-171193800	Enhancers	HUES64 Cell Line	embryonic stem cell
21	chr1:171190600-171191600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
22	chr1:171190600-171191600	Enhancers	NH-A	brain
23	chr1:171190600-171191800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
24	chr1:171190600-171191800	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
25	chr1:171190600-171191800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
26	chr1:171190600-171192200	Enhancers	Stomach Smooth Muscle	stomach
27	chr1:171190600-171192400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
28	chr1:171190600-171192400	Enhancers	Placenta	Placenta
29	chr1:171190600-171192400	Enhancers	NHDF-Ad	bronchial
30	chr1:171190600-171192600	Enhancers	ES-I3 Cell Line	embryonic stem cell
31	chr1:171190600-171192600	Enhancers	H1 Cell Line	embryonic stem cell
32	chr1:171190600-171192800	Enhancers	iPS-20b Cell Line	embryonic stem cell
33	chr1:171190600-171193000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
34	chr1:171190600-171193400	Enhancers	HUES48 Cell Line	embryonic stem cell
35	chr1:171190600-171194000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
36	chr1:171190600-171194200	Enhancers	Breast Myoepithelial Primary Cells	Breast
37	chr1:171190800-171192000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
38	chr1:171190800-171192600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
39	chr1:171190800-171192600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
40	chr1:171190800-171192600	Enhancers	Adipose Nuclei	Adipose
41	chr1:171190800-171192600	Enhancers	Fetal Stomach	stomach
42	chr1:171190800-171192800	Enhancers	iPS-15b Cell Line	embryonic stem cell
43	chr1:171190800-171193000	Enhancers	H9 Cell Line	embryonic stem cell
44	chr1:171190800-171193000	Enhancers	Stomach Mucosa	stomach
45	chr1:171191000-171191600	Enhancers	Duodenum Smooth Muscle	Duodenum
46	chr1:171191000-171191800	Enhancers	Fetal Intestine Small	intestine
47	chr1:171191000-171191800	Enhancers	Skeletal Muscle Male	skeletal muscle
48	chr1:171191000-171192000	Weak transcription	HSMMtube	muscle
49	chr1:171191000-171192200	Enhancers	iPS-18 Cell Line	embryonic stem cell
50	chr1:171191000-171192400	Enhancers	Aorta	Aorta

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links