Variant report

Variant	rs35777901
Chromosome Location	chr1:155437711-155437712
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 20 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:11)

rs_ID	r²[population]
rs10158907	1.00[ASW][hapmap];1.00[YRI][hapmap]
rs10752610	1.00[CHD][hapmap]
rs12064598	1.00[CHD][hapmap]
rs12752133	1.00[AMR][1000 genomes]
rs13373934	1.00[ASW][hapmap];0.89[MKK][hapmap];1.00[YRI][hapmap]
rs2230288	1.00[AMR][1000 genomes]
rs4971051	1.00[CHD][hapmap]
rs6664370	1.00[YRI][hapmap]
rs6673172	1.00[ASW][hapmap];0.89[MKK][hapmap];1.00[YRI][hapmap]
rs71628662	1.00[AMR][1000 genomes]
rs7519697	1.00[ASW][hapmap];1.00[MKK][hapmap];1.00[YRI][hapmap]

Variant overlapped rSNPs/rCNVs (count:9 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv529709	chr1:155154933-155757219	Strong transcription Weak transcription Flanking Active TSS Enhancers Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	450 gene(s)	inside rSNPs	diseases
2	nsv831636	chr1:155219223-155444864	Strong transcription Weak transcription Active TSS Flanking Active TSS Enhancers Genic enhancers ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	67 gene(s)	inside rSNPs	diseases
3	esv33869	chr1:155223283-155917961	Flanking Active TSS Strong transcription Weak transcription Active TSS Bivalent/Poised TSS Enhancers Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	187 gene(s)	inside rSNPs	diseases
4	esv1799856	chr1:155305059-155534616	Enhancers Weak transcription Genic enhancers Strong transcription Active TSS ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	41 gene(s)	inside rSNPs	diseases
5	esv1795662	chr1:155305059-155540660	Weak transcription ZNF genes & repeats Enhancers Strong transcription Flanking Active TSS Genic enhancers Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	41 gene(s)	inside rSNPs	diseases
6	esv1795478	chr1:155334933-155510824	Genic enhancers ZNF genes & repeats Flanking Active TSS Strong transcription Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
7	esv1803551	chr1:155334933-155522572	Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
8	esv1800974	chr1:155367680-155510824	Weak transcription Enhancers Genic enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
9	nsv872468	chr1:155413304-155549562	Active TSS Weak transcription Strong transcription Flanking Active TSS Enhancers Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	33 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:118 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:155362800-155442400	Weak transcription	Right Ventricle	heart
2	chr1:155364400-155450800	Weak transcription	HUVEC	blood vessel
3	chr1:155404600-155441400	Weak transcription	Esophagus	oesophagus
4	chr1:155408600-155444200	Weak transcription	Fetal Brain Male	brain
5	chr1:155408600-155448400	Weak transcription	Fetal Brain Female	brain
6	chr1:155408800-155441000	Weak transcription	H1 Cell Line	embryonic stem cell
7	chr1:155408800-155441000	Weak transcription	Stomach Smooth Muscle	stomach
8	chr1:155408800-155441200	Weak transcription	H9 Cell Line	embryonic stem cell
9	chr1:155408800-155447600	Weak transcription	Aorta	Aorta
10	chr1:155420600-155441000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
11	chr1:155420800-155439400	Weak transcription	Fetal Kidney	kidney
12	chr1:155421600-155441000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
13	chr1:155421600-155441600	Weak transcription	Brain Germinal Matrix	brain
14	chr1:155421800-155441200	Weak transcription	Ovary	ovary
15	chr1:155421800-155447800	Weak transcription	Lung	lung
16	chr1:155423000-155441200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
17	chr1:155423400-155441200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
18	chr1:155424400-155441000	Weak transcription	Fetal Muscle Leg	muscle
19	chr1:155424600-155462600	Weak transcription	Pancreas	Pancrea
20	chr1:155426200-155441000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
21	chr1:155426400-155448000	Weak transcription	Rectal Smooth Muscle	rectum
22	chr1:155426400-155455800	Weak transcription	Stomach Mucosa	stomach
23	chr1:155427000-155441000	Weak transcription	Small Intestine	intestine
24	chr1:155427400-155440600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
25	chr1:155427600-155441000	Weak transcription	HUES48 Cell Line	embryonic stem cell
26	chr1:155428200-155440600	Weak transcription	Brain Cingulate Gyrus	brain
27	chr1:155428200-155441000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
28	chr1:155428600-155441200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
29	chr1:155428600-155441200	Weak transcription	HepG2	liver
30	chr1:155428600-155451600	Weak transcription	Gastric	stomach
31	chr1:155429400-155441000	Weak transcription	HUES6 Cell Line	embryonic stem cell
32	chr1:155429800-155441000	Weak transcription	HUES64 Cell Line	embryonic stem cell
33	chr1:155429800-155441000	Weak transcription	Thymus	Thymus
34	chr1:155429800-155441200	Weak transcription	Fetal Stomach	stomach
35	chr1:155429800-155441200	Weak transcription	Rectal Mucosa Donor 31	rectum
36	chr1:155430400-155448200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
37	chr1:155432400-155438000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
38	chr1:155432400-155441000	Weak transcription	Primary neutrophils fromperipheralblood	blood
39	chr1:155432400-155441000	Weak transcription	Cortex derived primary cultured neurospheres	brain
40	chr1:155432400-155441200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
41	chr1:155432400-155441200	Weak transcription	Duodenum Mucosa	Duodenum
42	chr1:155432400-155441200	Weak transcription	Fetal Lung	lung
43	chr1:155432400-155441200	Weak transcription	Fetal Muscle Trunk	muscle
44	chr1:155432400-155441200	Weak transcription	Rectal Mucosa Donor 29	rectum
45	chr1:155432600-155441000	Weak transcription	Placenta	Placenta
46	chr1:155432600-155441200	Weak transcription	K562	blood
47	chr1:155433000-155441000	Weak transcription	Dnd41	blood
48	chr1:155433400-155437800	Enhancers	Osteobl	bone
49	chr1:155433400-155438000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
50	chr1:155433600-155439600	Weak transcription	Fetal Intestine Small	intestine

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