Variant report

Variant	rs7563742
Chromosome Location	chr2:86428218-86428219
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr2:86420213..86424453-chr2:86424933..86430971,16	MCF-7	breast:

Variant related genes	Relation type
ENSG00000132305	Chromatin interaction
ENSG00000265420	Chromatin interaction
ENSG00000273080	Chromatin interaction

Extended variants
information (count: 143 )
Associated
traits (count: 7 )

rSNPs within LD-proxies of this variant (count:122)

rs_ID	r²[population]
rs10170676	0.90[AFR][1000 genomes];0.96[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10175330	0.92[CEU][hapmap];0.82[CHB][hapmap];0.91[EUR][1000 genomes]
rs10184246	0.84[EUR][1000 genomes]
rs10184462	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.96[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10187150	0.89[CEU][hapmap];0.82[CHB][hapmap];0.81[EUR][1000 genomes]
rs10188059	0.91[EUR][1000 genomes]
rs10195199	0.93[CEU][hapmap];0.89[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs10200018	0.87[EUR][1000 genomes]
rs10202995	0.87[EUR][1000 genomes]
rs10208602	0.93[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs10496318	0.93[CEU][hapmap];0.82[CHB][hapmap];0.88[EUR][1000 genomes]
rs1057893	0.92[CEU][hapmap];0.82[CHB][hapmap];0.87[EUR][1000 genomes]
rs10901	0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11395	0.89[CEU][hapmap];0.82[EUR][1000 genomes]
rs11884038	0.91[EUR][1000 genomes]
rs11885380	0.93[CEU][hapmap];0.82[CHB][hapmap];0.92[EUR][1000 genomes]
rs11897696	0.91[EUR][1000 genomes]
rs11899254	0.93[CEU][hapmap];0.82[CHB][hapmap];0.92[EUR][1000 genomes]
rs11900161	0.85[CEU][hapmap]
rs12151585	0.88[EUR][1000 genomes]
rs12465983	0.87[EUR][1000 genomes]
rs12469363	0.88[EUR][1000 genomes]
rs12469762	0.93[CEU][hapmap];0.82[CHB][hapmap];0.91[EUR][1000 genomes]
rs12475079	0.93[CEU][hapmap];0.82[CHB][hapmap];0.91[EUR][1000 genomes]
rs12475126	0.93[CEU][hapmap];0.82[CHB][hapmap];0.91[EUR][1000 genomes]
rs12477274	0.92[CEU][hapmap];0.82[CHB][hapmap];0.88[EUR][1000 genomes]
rs12478097	0.93[CEU][hapmap];0.82[CHB][hapmap];0.88[EUR][1000 genomes]
rs12478369	0.87[EUR][1000 genomes]
rs12714170	0.87[EUR][1000 genomes]
rs12714171	0.93[CEU][hapmap];0.82[CHB][hapmap];0.88[EUR][1000 genomes]
rs12714172	0.93[CEU][hapmap];0.82[CHB][hapmap];0.92[EUR][1000 genomes]
rs12714173	0.96[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12714174	0.96[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12714175	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12714177	1.00[CEU][hapmap];1.00[CHB][hapmap];0.92[JPT][hapmap];1.00[YRI][hapmap];0.96[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12714178	0.88[EUR][1000 genomes]
rs12994382	0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12996308	0.92[CEU][hapmap];0.82[CHB][hapmap];0.92[EUR][1000 genomes]
rs12998025	0.81[EUR][1000 genomes]
rs12998164	0.88[EUR][1000 genomes]
rs13001470	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13007807	0.90[EUR][1000 genomes]
rs13010906	0.91[EUR][1000 genomes]
rs13011498	0.90[EUR][1000 genomes]
rs13013916	0.84[EUR][1000 genomes]
rs13019073	0.83[EUR][1000 genomes]
rs13024123	0.82[CHB][hapmap];1.00[JPT][hapmap]
rs13024884	0.87[EUR][1000 genomes]
rs13027248	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13028023	0.83[JPT][hapmap]
rs13032876	0.95[ASN][1000 genomes]
rs13035593	0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1424522	0.89[CEU][hapmap];0.82[CHB][hapmap];0.80[EUR][1000 genomes]
rs1540391	0.92[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[AMR][1000 genomes];0.95[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs17027013	0.92[CEU][hapmap];0.82[CHB][hapmap];0.91[EUR][1000 genomes]
rs17551815	0.91[EUR][1000 genomes]
rs2002250	0.81[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs2241438	0.89[CEU][hapmap];0.82[CHB][hapmap];0.82[EUR][1000 genomes]
rs2278083	0.93[CEU][hapmap];0.82[CHB][hapmap];0.88[EUR][1000 genomes]
rs2278536	0.82[CHB][hapmap];1.00[JPT][hapmap]
rs2288113	0.92[CEU][hapmap];0.82[CHB][hapmap];0.88[EUR][1000 genomes]
rs2288114	0.87[EUR][1000 genomes]
rs2288115	0.93[CEU][hapmap];0.82[CHB][hapmap];0.87[EUR][1000 genomes]
rs2367203	0.92[CEU][hapmap];0.82[CHB][hapmap];0.88[EUR][1000 genomes]
rs2367204	0.93[CEU][hapmap];0.82[CHB][hapmap];0.88[EUR][1000 genomes]
rs34263823	0.83[EUR][1000 genomes]
rs35615768	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3770059	0.82[CEU][hapmap];0.92[JPT][hapmap];0.83[ASN][1000 genomes]
rs3770060	0.88[EUR][1000 genomes]
rs3770061	0.88[EUR][1000 genomes]
rs3770062	0.93[CEU][hapmap];0.82[CHB][hapmap];0.88[EUR][1000 genomes]
rs3770065	0.93[CEU][hapmap];0.82[CHB][hapmap];0.88[EUR][1000 genomes]
rs3770067	0.93[CEU][hapmap];0.82[CHB][hapmap];0.88[EUR][1000 genomes]
rs4374375	0.92[CEU][hapmap];0.82[CHB][hapmap];0.92[EUR][1000 genomes]
rs4402761	0.92[CEU][hapmap];0.82[CHB][hapmap];0.92[EUR][1000 genomes]
rs4422155	0.92[CEU][hapmap];0.82[CHB][hapmap];0.92[EUR][1000 genomes]
rs4450596	0.92[CEU][hapmap];0.82[CHB][hapmap];0.92[EUR][1000 genomes]
rs4544439	0.92[CEU][hapmap];0.82[CHB][hapmap];0.92[EUR][1000 genomes]
rs62150072	0.87[EUR][1000 genomes]
rs62150074	0.88[EUR][1000 genomes]
rs6547660	0.86[EUR][1000 genomes]
rs6547661	0.93[CEU][hapmap];0.82[CHB][hapmap];0.87[EUR][1000 genomes]
rs6547662	0.87[EUR][1000 genomes]
rs6547663	0.87[EUR][1000 genomes]
rs6547665	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.93[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6707029	0.88[CEU][hapmap];0.87[EUR][1000 genomes]
rs6719136	0.92[EUR][1000 genomes]
rs6725046	0.85[CEU][hapmap]
rs6725372	0.93[CEU][hapmap];0.82[CHB][hapmap];0.87[EUR][1000 genomes]
rs6729732	0.92[CEU][hapmap];0.82[CHB][hapmap];0.88[EUR][1000 genomes]
rs6730226	0.91[EUR][1000 genomes]
rs6731535	0.86[EUR][1000 genomes]
rs6731995	0.92[CEU][hapmap];0.82[CHB][hapmap];0.88[EUR][1000 genomes]
rs6735014	0.82[CHB][hapmap];1.00[JPT][hapmap]
rs6737950	0.92[CEU][hapmap];0.82[CHB][hapmap]
rs6740287	0.88[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6747474	0.92[EUR][1000 genomes]
rs6749090	0.82[CEU][hapmap]
rs6757387	0.93[CEU][hapmap];0.82[CHB][hapmap];0.88[EUR][1000 genomes]
rs715334	0.89[CEU][hapmap];0.82[CHB][hapmap];0.82[EUR][1000 genomes]
rs7422930	0.92[CEU][hapmap];0.89[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs7560376	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.90[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7561589	0.87[EUR][1000 genomes]
rs7566721	0.93[CEU][hapmap];0.82[CHB][hapmap];0.88[EUR][1000 genomes]
rs7566961	0.91[EUR][1000 genomes]
rs7569853	0.86[EUR][1000 genomes]
rs7572386	0.82[CHB][hapmap];1.00[JPT][hapmap]
rs7588325	0.93[CEU][hapmap];0.91[EUR][1000 genomes]
rs7590445	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.93[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7608547	0.85[EUR][1000 genomes]
rs7609008	0.92[CEU][hapmap];0.82[CHB][hapmap];0.87[EUR][1000 genomes]
rs8244	0.89[CEU][hapmap];0.82[CHB][hapmap];0.84[EUR][1000 genomes]
rs876242	0.89[CEU][hapmap];0.82[CHB][hapmap];0.83[EUR][1000 genomes]
rs9309632	0.93[CEU][hapmap];0.82[CHB][hapmap];0.91[EUR][1000 genomes]
rs9309633	0.96[CEU][hapmap];0.82[CHB][hapmap];0.91[EUR][1000 genomes]
rs9646999	0.91[EUR][1000 genomes]
rs9653508	0.82[CEU][hapmap];0.80[EUR][1000 genomes]
rs9653569	0.89[CEU][hapmap];0.82[CHB][hapmap];0.92[EUR][1000 genomes]
rs9789526	0.92[AFR][1000 genomes];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs9808316	0.87[AFR][1000 genomes];0.98[AMR][1000 genomes];0.94[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs9917140	0.88[EUR][1000 genomes]
rs9973320	0.85[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:21 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2751903	chr2:86253542-86505453	Active TSS Genic enhancers Weak transcription Strong transcription Enhancers ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	47 gene(s)	inside rSNPs	diseases
2	nsv531380	chr2:86253552-86469217	Enhancers Active TSS Weak transcription Flanking Active TSS Strong transcription Genic enhancers ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	47 gene(s)	inside rSNPs	diseases
3	nsv1007474	chr2:86281967-86505453	Enhancers Flanking Active TSS Strong transcription Weak transcription Transcr. at gene 5' and 3' Genic enhancers Active TSS Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	47 gene(s)	inside rSNPs	diseases
4	nsv997563	chr2:86281967-86506132	Genic enhancers Weak transcription Strong transcription Flanking Active TSS Enhancers Active TSS 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	47 gene(s)	inside rSNPs	diseases
5	nsv1008924	chr2:86282722-86499402	Genic enhancers Strong transcription Weak transcription ZNF genes & repeats Enhancers Active TSS Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	47 gene(s)	inside rSNPs	diseases
6	nsv999956	chr2:86285944-86505453	Active TSS Weak transcription Enhancers Flanking Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	47 gene(s)	inside rSNPs	diseases
7	nsv1012768	chr2:86285944-86506132	Strong transcription Weak transcription Genic enhancers Flanking Active TSS Enhancers ZNF genes & repeats Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	47 gene(s)	inside rSNPs	diseases
8	nsv1003207	chr2:86286314-86496732	Genic enhancers Strong transcription Weak transcription Flanking Active TSS Active TSS Enhancers ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	47 gene(s)	inside rSNPs	diseases
9	nsv1000441	chr2:86286314-86508168	Enhancers Weak transcription Strong transcription Genic enhancers Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	47 gene(s)	inside rSNPs	diseases
10	nsv535808	chr2:86286314-86508168	Genic enhancers Weak transcription Flanking Active TSS Strong transcription Enhancers Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	47 gene(s)	inside rSNPs	diseases
11	nsv1004442	chr2:86286480-86506132	Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Active TSS Genic enhancers Strong transcription Enhancers ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	47 gene(s)	inside rSNPs	diseases
12	nsv916616	chr2:86289130-86509326	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	47 gene(s)	inside rSNPs	diseases
13	nsv458563	chr2:86292341-86507688	Weak transcription Enhancers Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	47 gene(s)	inside rSNPs	diseases
14	nsv582370	chr2:86292341-86507688	Flanking Active TSS Active TSS Strong transcription Weak transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	47 gene(s)	inside rSNPs	diseases
15	nsv1009140	chr2:86294939-86506132	Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	47 gene(s)	inside rSNPs	diseases
16	nsv582371	chr2:86296566-86507688	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers Bivalent Enhancer Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	47 gene(s)	inside rSNPs	diseases
17	nsv531381	chr2:86301091-86478346	Active TSS Strong transcription Enhancers Weak transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	47 gene(s)	inside rSNPs	diseases
18	nsv1001157	chr2:86301440-86508168	Strong transcription Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	47 gene(s)	inside rSNPs	diseases
19	esv3412938	chr2:86370969-86867936	Strong transcription Enhancers Genic enhancers Weak transcription Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	77 gene(s)	inside rSNPs	diseases
20	nsv458574	chr2:86385728-86507688	Enhancers Flanking Active TSS Genic enhancers Weak transcription ZNF genes & repeats Strong transcription Active TSS 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	36 gene(s)	inside rSNPs	diseases
21	nsv582372	chr2:86385728-86507688	Enhancers Genic enhancers Weak transcription Strong transcription Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	36 gene(s)	inside rSNPs	diseases

mRNA abundance (count:7)

SNP	Gene	Cis/trans	Tissue	Source
rs7563742	IMMT	cis	Whole Blood	GTEx
rs7563742	IMMT	cis	multi-tissue	Pritchard
rs7563742	MRPL35	cis	uninvolved skin	skin_eQTL
rs7563742	MRPL35	Cis_1M	lymphoblastoid	RTeQTL
rs7563742	IMMT	cis	Esophagus Muscularis	GTEx
rs7563742	IMMT	Cis_1M	lymphoblastoid	RTeQTL
rs7563742	IMMT	cis	Artery Aorta	GTEx

Chromatin state (count:126 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:86425800-86429800	Active TSS	GM12878-XiMat	blood
2	chr2:86426000-86428400	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
3	chr2:86426200-86428800	Active TSS	K562	blood
4	chr2:86427000-86433800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
5	chr2:86427200-86428400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
6	chr2:86427200-86431200	Weak transcription	Sigmoid Colon	Sigmoid Colon
7	chr2:86427200-86432600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
8	chr2:86427200-86433400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
9	chr2:86427200-86433400	Weak transcription	Gastric	stomach
10	chr2:86427200-86433600	Weak transcription	Esophagus	oesophagus
11	chr2:86427200-86433600	Weak transcription	Lung	lung
12	chr2:86427200-86433600	Weak transcription	Pancreas	Pancrea
13	chr2:86427200-86433600	Weak transcription	Stomach Mucosa	stomach
14	chr2:86427200-86434600	Weak transcription	Small Intestine	intestine
15	chr2:86427200-86444200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
16	chr2:86427200-86450200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
17	chr2:86427400-86428400	Enhancers	Primary T helper naive cells fromperipheralblood	blood
18	chr2:86427400-86428400	Enhancers	Primary T regulatory cells fromperipheralblood	blood
19	chr2:86427400-86428400	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
20	chr2:86427400-86428400	Enhancers	Brain Hippocampus Middle	brain
21	chr2:86427400-86428400	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
22	chr2:86427400-86428400	Enhancers	Colonic Mucosa	Colon
23	chr2:86427400-86428400	Enhancers	Osteobl	bone
24	chr2:86427400-86428800	Enhancers	Brain Substantia Nigra	brain
25	chr2:86427400-86429000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
26	chr2:86427400-86429000	Weak transcription	H9 Cell Line	embryonic stem cell
27	chr2:86427400-86429200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
28	chr2:86427400-86429200	Enhancers	Primary T helper cells fromperipheralblood	blood
29	chr2:86427400-86429200	Enhancers	Colon Smooth Muscle	Colon
30	chr2:86427400-86429400	Enhancers	Primary T killer naive cells fromperipheralblood	blood
31	chr2:86427400-86431200	Weak transcription	Fetal Intestine Small	intestine
32	chr2:86427400-86432400	Weak transcription	Fetal Muscle Leg	muscle
33	chr2:86427400-86432600	Weak transcription	Primary T cells fromperipheralblood	blood
34	chr2:86427400-86432600	Weak transcription	Aorta	Aorta
35	chr2:86427400-86432800	Weak transcription	Placenta	Placenta
36	chr2:86427400-86433600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
37	chr2:86427400-86433600	Weak transcription	Ovary	ovary
38	chr2:86427400-86433800	Weak transcription	HSMMtube	muscle
39	chr2:86427400-86448200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
40	chr2:86427600-86428400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
41	chr2:86427600-86428400	Enhancers	Primary T helper cells PMA-I stimulated	--
42	chr2:86427600-86428400	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
43	chr2:86427600-86428400	Enhancers	Fetal Brain Female	brain
44	chr2:86427600-86428400	Enhancers	Fetal Intestine Large	intestine
45	chr2:86427600-86428400	Enhancers	Skeletal Muscle Female	skeletal muscle
46	chr2:86427600-86428400	Enhancers	HSMM	muscle
47	chr2:86427600-86429200	Enhancers	Muscle Satellite Cultured Cells	--
48	chr2:86427600-86429200	Enhancers	Brain Cingulate Gyrus	brain
49	chr2:86427600-86429200	Enhancers	Pancreatic Islets	Pancreatic Islet
50	chr2:86427600-86429400	Enhancers	Liver	Liver

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