Variant report

Variant	rs73822610
Chromosome Location	chr4:62383723-62383724
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 27 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:21)

rs_ID	r²[population]
rs2088113	0.84[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs55636236	0.84[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs55773246	0.95[AFR][1000 genomes];0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs55939610	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs56338474	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs59130415	0.84[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs60655392	0.83[EUR][1000 genomes]
rs73822609	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs73822617	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs73822619	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs73822621	0.95[AFR][1000 genomes];0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs73822622	0.95[AFR][1000 genomes];0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs73822651	0.84[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs73822652	0.84[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs73822688	0.84[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs73822690	0.83[EUR][1000 genomes]
rs73822691	0.83[EUR][1000 genomes]
rs73822692	0.83[EUR][1000 genomes]
rs7660587	0.83[EUR][1000 genomes]
rs9917973	1.00[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs9918049	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.89[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	nsv868844	chr4:62241702-62497248	Weak transcription Enhancers Bivalent/Poised TSS Strong transcription Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
2	esv2753138	chr4:62271444-62442507	Enhancers Weak transcription Bivalent Enhancer ZNF genes & repeats Active TSS Flanking Active TSS Bivalent/Poised TSS Strong transcription	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
3	nsv1005770	chr4:62344379-62398798	Weak transcription Enhancers Active TSS ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Strong transcription	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
4	nsv537109	chr4:62344379-62398798	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Strong transcription Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
5	nsv461377	chr4:62368762-62883431	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Genic enhancers Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
6	nsv594328	chr4:62368762-62883431	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Bivalent/Poised TSS Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:24 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:62373600-62385600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr4:62378000-62386400	Weak transcription	Stomach Mucosa	stomach
3	chr4:62380000-62385800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
4	chr4:62380800-62384200	Weak transcription	Brain Angular Gyrus	brain
5	chr4:62381000-62384200	Weak transcription	Brain Inferior Temporal Lobe	brain
6	chr4:62381000-62386400	Weak transcription	Brain Anterior Caudate	brain
7	chr4:62381400-62386600	Weak transcription	HMEC	breast
8	chr4:62381800-62386200	Weak transcription	NHEK	skin
9	chr4:62382600-62385200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
10	chr4:62382600-62385600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
11	chr4:62383200-62384400	Enhancers	Fetal Heart	heart
12	chr4:62383200-62397800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr4:62383400-62384400	Weak transcription	H1 Cell Line	embryonic stem cell
14	chr4:62383400-62384400	Enhancers	iPS-15b Cell Line	embryonic stem cell
15	chr4:62383400-62385200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
16	chr4:62383400-62385600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
17	chr4:62383400-62385800	Weak transcription	HUES6 Cell Line	embryonic stem cell
18	chr4:62383400-62386800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
19	chr4:62383400-62387200	Enhancers	HUES48 Cell Line	embryonic stem cell
20	chr4:62383400-62387400	Enhancers	HUES64 Cell Line	embryonic stem cell
21	chr4:62383400-62388600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
22	chr4:62383400-62388600	Weak transcription	Placenta Amnion	Placenta Amnion
23	chr4:62383600-62384200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
24	chr4:62383600-62384200	Weak transcription	Gastric	stomach

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links