Variant report

Variant	rs320075
Chromosome Location	chr13:93868944-93868945
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 74 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:69)

rs_ID	r²[population]
rs16948474	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs1810933	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs1855274	0.91[ASW][hapmap];0.89[LWK][hapmap];0.95[YRI][hapmap];0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs1855275	0.95[YRI][hapmap];0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs223307	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2388917	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2780374	0.95[AFR][1000 genomes]
rs2780381	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2780382	0.91[ASW][hapmap];0.96[LWK][hapmap];0.91[MKK][hapmap];0.95[YRI][hapmap];0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2781051	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2781052	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs319517	0.85[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs319518	0.95[YRI][hapmap];0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs319520	0.91[ASW][hapmap];0.86[LWK][hapmap];0.89[MKK][hapmap];0.95[YRI][hapmap];0.89[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs319521	0.95[YRI][hapmap];0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs320070	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs320071	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs320072	0.93[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs320076	0.91[ASW][hapmap];0.90[LWK][hapmap];0.85[MKK][hapmap];0.95[YRI][hapmap];0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs320078	0.95[YRI][hapmap];0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs320079	0.95[YRI][hapmap];0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs320080	0.95[YRI][hapmap];0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs320081	0.95[YRI][hapmap];0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs364631	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs366378	0.94[AFR][1000 genomes]
rs367924	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs368555	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs371381	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs374389	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs376830	0.82[ASW][hapmap];0.97[LWK][hapmap];0.93[MKK][hapmap];0.95[YRI][hapmap];0.88[AFR][1000 genomes]
rs376851	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs381662	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs385054	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs387992	0.95[YRI][hapmap];0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs389587	0.95[YRI][hapmap];0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs397442	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs415326	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs417537	0.86[LWK][hapmap];0.87[MKK][hapmap]
rs417815	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs418948	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs420913	0.95[YRI][hapmap];0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs425955	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs426342	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs426397	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs426787	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs427399	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs431476	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs432632	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs432800	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs433129	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs433135	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs437435	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs437703	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs437913	0.93[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs438139	0.95[YRI][hapmap];0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs439216	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs443603	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs444365	1.00[AMR][1000 genomes]
rs448518	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs450509	0.95[YRI][hapmap];0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs450732	0.95[YRI][hapmap];0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs451048	0.95[YRI][hapmap];0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs454092	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs475566	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs489911	0.80[YRI][hapmap]
rs521884	0.95[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs549385	0.95[YRI][hapmap];0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs914865	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs914866	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv869070	chr13:93347616-94286933	Enhancers Weak transcription Genic enhancers Bivalent Enhancer Flanking Active TSS Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
2	nsv832682	chr13:93700861-93874801	Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Bivalent/Poised TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
3	nsv900916	chr13:93814026-93869041	Active TSS Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
4	nsv1053035	chr13:93842576-94229732	Enhancers Flanking Active TSS Active TSS Weak transcription ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
5	nsv541880	chr13:93842576-94229732	Active TSS Flanking Active TSS Weak transcription Enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Strong transcription Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:22 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:93866600-93869000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr13:93867800-93869400	Enhancers	H1 Cell Line	embryonic stem cell
3	chr13:93868200-93869000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
4	chr13:93868200-93870800	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
5	chr13:93868200-93872400	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
6	chr13:93868400-93869000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr13:93868400-93869200	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
8	chr13:93868400-93870600	Enhancers	HepG2	liver
9	chr13:93868600-93869000	Flanking Active TSS	H9 Cell Line	embryonic stem cell
10	chr13:93868600-93869000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
11	chr13:93868600-93870600	Flanking Active TSS	HUES64 Cell Line	embryonic stem cell
12	chr13:93868800-93869000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr13:93868800-93869000	Flanking Active TSS	iPS-15b Cell Line	embryonic stem cell
14	chr13:93868800-93869200	Flanking Active TSS	ES-I3 Cell Line	embryonic stem cell
15	chr13:93868800-93869200	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell
16	chr13:93868800-93869200	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
17	chr13:93868800-93869800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
18	chr13:93868800-93869800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
19	chr13:93868800-93869800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
20	chr13:93868800-93870000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
21	chr13:93868800-93871200	Enhancers	HMEC	breast
22	chr13:93868800-93876800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links