Variant report

Variant	rs7950900
Chromosome Location	chr11:68293545-68293546
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr11:68274527..68278088-chr11:68291601..68295051,3	MCF-7	breast:
2	chr11:68247315..68249122-chr11:68293353..68295146,2	K562	blood:
3	chr11:68286980..68288583-chr11:68292044..68293926,2	K562	blood:

Variant related genes	Relation type
ENSG00000110075	Chromatin interaction

Extended variants
information (count: 152 )
Associated
traits (count: 6 )

rSNPs within LD-proxies of this variant (count:138)

rs_ID	r²[population]
rs10047412	0.91[ASN][1000 genomes]
rs10047482	0.89[ASN][1000 genomes]
rs10047483	0.89[ASN][1000 genomes]
rs10501398	0.92[CHB][hapmap];0.97[CHD][hapmap];0.89[JPT][hapmap];0.92[ASN][1000 genomes]
rs10750827	0.87[ASN][1000 genomes]
rs10791981	0.97[ASN][1000 genomes]
rs10791982	0.92[ASN][1000 genomes]
rs10896326	0.88[ASN][1000 genomes]
rs10896327	0.88[ASN][1000 genomes]
rs10896328	0.94[ASN][1000 genomes]
rs10896329	0.93[ASN][1000 genomes]
rs10896330	0.93[ASN][1000 genomes]
rs10896331	0.99[ASN][1000 genomes]
rs10896334	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.87[AFR][1000 genomes];0.99[ASN][1000 genomes]
rs10896337	1.00[CHB][hapmap];0.94[JPT][hapmap];0.81[YRI][hapmap];0.99[ASN][1000 genomes]
rs10896338	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.81[YRI][hapmap];0.97[ASN][1000 genomes]
rs10896339	1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[ASN][1000 genomes]
rs10896340	0.93[ASN][1000 genomes]
rs10896341	1.00[CHB][hapmap];1.00[JPT][hapmap];0.82[YRI][hapmap];0.98[ASN][1000 genomes]
rs10896342	0.98[ASN][1000 genomes]
rs10896343	0.98[ASN][1000 genomes]
rs10896346	0.96[ASN][1000 genomes]
rs10896347	0.92[CHB][hapmap];0.97[CHD][hapmap];1.00[JPT][hapmap];0.85[YRI][hapmap];0.96[ASN][1000 genomes]
rs10896348	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs10896350	0.89[ASN][1000 genomes]
rs10896351	0.89[ASN][1000 genomes]
rs11228251	1.00[CHB][hapmap];1.00[CHD][hapmap];0.83[GIH][hapmap];1.00[JPT][hapmap];0.97[ASN][1000 genomes]
rs11228256	1.00[CHB][hapmap];0.97[CHD][hapmap];0.83[GIH][hapmap];1.00[JPT][hapmap];0.95[YRI][hapmap];0.93[ASN][1000 genomes]
rs11228258	1.00[CHB][hapmap];1.00[CHD][hapmap];0.83[GIH][hapmap];1.00[JPT][hapmap];0.98[MKK][hapmap];0.86[YRI][hapmap];0.95[ASN][1000 genomes]
rs11228262	1.00[CHB][hapmap];1.00[JPT][hapmap];0.81[YRI][hapmap];0.97[ASN][1000 genomes]
rs11228268	0.97[ASN][1000 genomes]
rs11228269	1.00[CHB][hapmap];0.97[CHD][hapmap];0.83[GIH][hapmap];1.00[JPT][hapmap];0.86[YRI][hapmap];0.97[ASN][1000 genomes]
rs11228275	0.92[ASN][1000 genomes]
rs11228276	0.96[ASN][1000 genomes]
rs11228277	1.00[ASN][1000 genomes]
rs11228278	0.99[ASN][1000 genomes]
rs11228279	0.88[CHB][hapmap];1.00[JPT][hapmap];0.93[ASN][1000 genomes]
rs11228284	1.00[CHB][hapmap];1.00[JPT][hapmap];0.81[YRI][hapmap];0.98[ASN][1000 genomes]
rs11228287	1.00[CHB][hapmap];1.00[JPT][hapmap];0.80[YRI][hapmap];0.98[ASN][1000 genomes]
rs11228288	0.91[ASN][1000 genomes]
rs11228291	0.95[ASN][1000 genomes]
rs11228292	1.00[CHB][hapmap];0.97[CHD][hapmap];1.00[JPT][hapmap];0.81[YRI][hapmap];0.96[ASN][1000 genomes]
rs11228293	1.00[CHB][hapmap];1.00[JPT][hapmap];0.81[YRI][hapmap];0.93[ASN][1000 genomes]
rs11822059	0.92[CHB][hapmap];0.94[CHD][hapmap];1.00[JPT][hapmap];0.93[ASN][1000 genomes]
rs1193699	0.92[CHB][hapmap];1.00[JPT][hapmap];0.88[ASN][1000 genomes]
rs12226585	0.92[CHB][hapmap];0.89[JPT][hapmap];0.89[ASN][1000 genomes]
rs12271290	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.97[LWK][hapmap];1.00[MKK][hapmap];1.00[YRI][hapmap];0.89[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs12272917	1.00[CHB][hapmap];1.00[JPT][hapmap];0.80[YRI][hapmap];0.95[ASN][1000 genomes]
rs12274114	0.95[ASN][1000 genomes]
rs12277225	0.89[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs12281742	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs12283755	1.00[CHB][hapmap];0.97[CHD][hapmap];1.00[JPT][hapmap];0.81[YRI][hapmap];0.96[ASN][1000 genomes]
rs12284933	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.81[YRI][hapmap];1.00[ASN][1000 genomes]
rs12285993	0.98[ASN][1000 genomes]
rs12294029	1.00[CHB][hapmap];1.00[JPT][hapmap];0.90[YRI][hapmap];0.97[ASN][1000 genomes]
rs12360903	0.93[ASN][1000 genomes]
rs12363722	0.93[ASN][1000 genomes]
rs12364620	0.93[ASN][1000 genomes]
rs12365160	0.93[ASN][1000 genomes]
rs12941	0.96[ASN][1000 genomes]
rs17603185	0.95[ASN][1000 genomes]
rs2155730	1.00[CHB][hapmap];1.00[JPT][hapmap];0.97[ASN][1000 genomes]
rs2156463	0.89[ASN][1000 genomes]
rs2236708	1.00[CHB][hapmap];0.97[CHD][hapmap];1.00[JPT][hapmap];0.81[YRI][hapmap];0.95[ASN][1000 genomes]
rs2282563	1.00[CHB][hapmap];1.00[JPT][hapmap];0.81[YRI][hapmap];0.98[ASN][1000 genomes]
rs2472420	0.85[ASN][1000 genomes]
rs2510384	0.92[ASN][1000 genomes]
rs2510392	0.85[ASN][1000 genomes]
rs2513277	0.92[CHB][hapmap];0.93[CHD][hapmap];1.00[JPT][hapmap];0.91[ASN][1000 genomes]
rs2840367	0.92[CHB][hapmap];0.94[CHD][hapmap];0.89[JPT][hapmap];0.92[ASN][1000 genomes]
rs3018713	0.87[ASN][1000 genomes]
rs3740628	0.92[CHB][hapmap];0.97[CHD][hapmap];1.00[JPT][hapmap];0.91[ASN][1000 genomes]
rs3740629	1.00[CHB][hapmap];0.97[CHD][hapmap];1.00[JPT][hapmap];0.81[YRI][hapmap];0.98[ASN][1000 genomes]
rs3740631	1.00[CHB][hapmap];0.97[CHD][hapmap];1.00[JPT][hapmap];0.81[YRI][hapmap];0.98[ASN][1000 genomes]
rs3758643	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.97[ASN][1000 genomes]
rs3824850	0.98[ASN][1000 genomes]
rs3867143	1.00[CHB][hapmap];0.83[JPT][hapmap]
rs4084149	0.97[ASN][1000 genomes]
rs4316515	1.00[CHB][hapmap];0.97[CHD][hapmap];1.00[JPT][hapmap];0.81[YRI][hapmap];0.98[ASN][1000 genomes]
rs4340059	0.91[ASN][1000 genomes]
rs488381	0.90[CHB][hapmap];0.89[JPT][hapmap];0.91[ASN][1000 genomes]
rs498782	0.84[ASN][1000 genomes]
rs4988291	1.00[CHB][hapmap];0.97[CHD][hapmap];1.00[JPT][hapmap];0.80[YRI][hapmap];0.96[ASN][1000 genomes]
rs55767696	0.98[ASN][1000 genomes]
rs55816191	0.97[ASN][1000 genomes]
rs55883802	0.97[ASN][1000 genomes]
rs55953412	0.98[ASN][1000 genomes]
rs59056571	0.97[ASN][1000 genomes]
rs596494	0.87[ASN][1000 genomes]
rs60212556	0.98[ASN][1000 genomes]
rs61391279	0.87[ASN][1000 genomes]
rs624003	0.84[CHB][hapmap];0.94[CHD][hapmap];1.00[JPT][hapmap];0.83[ASN][1000 genomes]
rs643609	0.89[ASN][1000 genomes]
rs6591340	1.00[CHB][hapmap];1.00[JPT][hapmap];0.81[YRI][hapmap];0.98[ASN][1000 genomes]
rs6591341	1.00[CHB][hapmap];0.97[CHD][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs6591344	1.00[CHB][hapmap];1.00[JPT][hapmap];0.83[YRI][hapmap];0.96[ASN][1000 genomes]
rs6591346	0.95[ASN][1000 genomes]
rs66752716	0.97[ASN][1000 genomes]
rs67005337	0.98[ASN][1000 genomes]
rs67101048	0.97[ASN][1000 genomes]
rs67605986	0.98[ASN][1000 genomes]
rs67947146	0.98[ASN][1000 genomes]
rs7101691	0.95[ASN][1000 genomes]
rs7102273	1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[YRI][hapmap];0.96[ASN][1000 genomes]
rs7102898	1.00[CHB][hapmap];0.97[CHD][hapmap];1.00[JPT][hapmap];0.81[YRI][hapmap];0.98[ASN][1000 genomes]
rs7104345	1.00[CHB][hapmap];1.00[JPT][hapmap];0.81[YRI][hapmap];0.98[ASN][1000 genomes]
rs7104877	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.97[ASN][1000 genomes]
rs7106010	0.98[ASN][1000 genomes]
rs7106259	1.00[CHB][hapmap];0.97[CHD][hapmap];1.00[JPT][hapmap];0.86[YRI][hapmap];0.97[ASN][1000 genomes]
rs7106339	0.93[ASN][1000 genomes]
rs7107622	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs7108376	0.92[CHB][hapmap];0.97[CHD][hapmap];1.00[JPT][hapmap];0.91[ASN][1000 genomes]
rs7109294	1.00[CHB][hapmap];0.97[CHD][hapmap];1.00[JPT][hapmap];0.81[YRI][hapmap];0.98[ASN][1000 genomes]
rs7113287	1.00[CHB][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs7115374	0.98[ASN][1000 genomes]
rs7116899	0.96[ASN][1000 genomes]
rs7116994	1.00[CHB][hapmap];1.00[JPT][hapmap];0.91[YRI][hapmap];0.95[ASN][1000 genomes]
rs7118897	1.00[CHB][hapmap];0.97[CHD][hapmap];1.00[JPT][hapmap]
rs7119422	0.92[CHB][hapmap];0.97[CHD][hapmap];0.89[JPT][hapmap];0.92[ASN][1000 genomes]
rs7120557	0.97[ASN][1000 genomes]
rs7120635	0.97[ASN][1000 genomes]
rs7120876	0.90[ASN][1000 genomes]
rs7123564	0.84[CHB][hapmap];0.94[CHD][hapmap];1.00[JPT][hapmap];0.96[ASN][1000 genomes]
rs7124078	1.00[CHB][hapmap];0.97[CHD][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];1.00[MKK][hapmap];1.00[YRI][hapmap];0.87[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs7126340	1.00[CHB][hapmap];1.00[JPT][hapmap];0.91[YRI][hapmap];0.97[ASN][1000 genomes]
rs7126451	0.92[CHB][hapmap];0.97[CHD][hapmap];1.00[JPT][hapmap];0.90[ASN][1000 genomes]
rs7127948	1.00[CHB][hapmap];1.00[JPT][hapmap];0.80[YRI][hapmap];0.96[ASN][1000 genomes]
rs7129248	0.90[ASN][1000 genomes]
rs73506204	0.96[ASN][1000 genomes]
rs73516862	0.97[ASN][1000 genomes]
rs73518807	0.96[ASN][1000 genomes]
rs7925275	1.00[CHB][hapmap];0.97[CHD][hapmap];0.83[GIH][hapmap];1.00[JPT][hapmap];0.81[YRI][hapmap];0.97[ASN][1000 genomes]
rs7927592	0.98[ASN][1000 genomes]
rs7936582	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.96[GIH][hapmap];1.00[JPT][hapmap];0.94[MEX][hapmap];0.95[TSI][hapmap];0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7944870	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.95[YRI][hapmap];0.96[ASN][1000 genomes]
rs871212	0.98[ASN][1000 genomes]
rs948315	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.92[LWK][hapmap];1.00[MKK][hapmap];0.86[YRI][hapmap];1.00[ASN][1000 genomes]
rs948316	1.00[CHB][hapmap];1.00[JPT][hapmap];0.80[YRI][hapmap];0.98[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:14 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv897858	chr11:68077238-68293545	Enhancers Weak transcription Flanking Active TSS Strong transcription Genic enhancers ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	25 gene(s)	inside rSNPs	diseases
2	nsv897860	chr11:68102000-68293545	Enhancers Weak transcription Flanking Active TSS Strong transcription Genic enhancers Active TSS 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	20 gene(s)	inside rSNPs	diseases
3	nsv1036561	chr11:68123135-68315685	Weak transcription Strong transcription Genic enhancers Enhancers ZNF genes & repeats Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
4	esv1792339	chr11:68199008-68299226	Enhancers Weak transcription Genic enhancers Strong transcription Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
5	esv1803199	chr11:68199008-68299226	Flanking Active TSS Weak transcription Active TSS Enhancers Strong transcription Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
6	esv1842405	chr11:68199008-68299226	Enhancers Strong transcription Weak transcription Genic enhancers Active TSS Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
7	esv3431317	chr11:68282676-68411867	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
8	esv3478641	chr11:68282679-68411856	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
9	esv3478652	chr11:68282679-68411856	Enhancers Genic enhancers Weak transcription Strong transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
10	esv3425206	chr11:68282708-68411817	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
11	esv3511614	chr11:68282726-68411806	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3' Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
12	esv3511615	chr11:68282726-68411806	Weak transcription Genic enhancers Strong transcription Enhancers Active TSS Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
13	esv3348204	chr11:68282891-68411839	Strong transcription Enhancers Weak transcription Genic enhancers Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
14	nsv832195	chr11:68286383-68474611	Strong transcription Weak transcription Enhancers Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	12 gene(s)	inside rSNPs	diseases

mRNA abundance (count:6)

SNP	Gene	Cis/trans	Tissue	Source
rs7950900	SHANK2	cis	cerebellum	SCAN
rs7950900	OR1K1	trans	parietal	SCAN
rs7950900	TM7SF2	cis	cerebellum	SCAN
rs7950900	CD248	cis	cerebellum	SCAN
rs7950900	C11orf85	cis	parietal	SCAN
rs7950900	CABP2	cis	cerebellum	SCAN

Chromatin state (count:127 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:68265200-68302600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr11:68268600-68303800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
3	chr11:68271000-68294600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr11:68274400-68296000	Weak transcription	Stomach Mucosa	stomach
5	chr11:68276000-68305600	Weak transcription	Fetal Brain Male	brain
6	chr11:68276600-68304000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
7	chr11:68277600-68336000	Strong transcription	Dnd41	blood
8	chr11:68283000-68358200	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
9	chr11:68284200-68297600	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
10	chr11:68285800-68295600	Strong transcription	GM12878-XiMat	blood
11	chr11:68285800-68295800	Strong transcription	Primary B cells from peripheral blood	blood
12	chr11:68286000-68295400	Strong transcription	Primary B cells from cord blood	blood
13	chr11:68286200-68300200	Strong transcription	Hela-S3	cervix
14	chr11:68286400-68296400	Strong transcription	HUES6 Cell Line	embryonic stem cell
15	chr11:68286400-68303200	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
16	chr11:68286600-68295200	Strong transcription	Primary monocytes fromperipheralblood	blood
17	chr11:68286600-68295200	Strong transcription	Monocytes-CD14+_RO01746	blood
18	chr11:68286600-68296400	Strong transcription	HSMM	muscle
19	chr11:68286600-68296600	Strong transcription	HUES48 Cell Line	embryonic stem cell
20	chr11:68286800-68294000	Strong transcription	Primary T cells from cord blood	blood
21	chr11:68286800-68294600	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
22	chr11:68286800-68295200	Strong transcription	K562	blood
23	chr11:68286800-68296000	Strong transcription	Fetal Thymus	thymus
24	chr11:68286800-68296600	Strong transcription	Liver	Liver
25	chr11:68286800-68297400	Strong transcription	iPS-20b Cell Line	embryonic stem cell
26	chr11:68287000-68296800	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
27	chr11:68287000-68297400	Strong transcription	Osteobl	bone
28	chr11:68287000-68299200	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
29	chr11:68287200-68294800	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
30	chr11:68287200-68296600	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
31	chr11:68287200-68297200	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
32	chr11:68287200-68298200	Strong transcription	HUES64 Cell Line	embryonic stem cell
33	chr11:68287200-68301200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
34	chr11:68288000-68296600	Genic enhancers	Primary T helper naive cells fromperipheralblood	blood
35	chr11:68288600-68309000	Weak transcription	Placenta Amnion	Placenta Amnion
36	chr11:68289000-68296600	Genic enhancers	Fetal Intestine Large	intestine
37	chr11:68289200-68294400	Genic enhancers	HUVEC	blood vessel
38	chr11:68290000-68294800	Weak transcription	Brain Germinal Matrix	brain
39	chr11:68290200-68296800	Strong transcription	Thymus	Thymus
40	chr11:68290400-68295600	Weak transcription	Pancreatic Islets	Pancreatic Islet
41	chr11:68290600-68294200	Genic enhancers	Colon Smooth Muscle	Colon
42	chr11:68290800-68295600	Genic enhancers	Breast Myoepithelial Primary Cells	Breast
43	chr11:68291000-68297000	Genic enhancers	Fetal Intestine Small	intestine
44	chr11:68291000-68297800	Strong transcription	iPS-18 Cell Line	embryonic stem cell
45	chr11:68291200-68294400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
46	chr11:68291400-68293600	Genic enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
47	chr11:68291400-68293600	Genic enhancers	Duodenum Mucosa	Duodenum
48	chr11:68291400-68293600	Enhancers	Duodenum Smooth Muscle	Duodenum
49	chr11:68291400-68293600	Enhancers	Skeletal Muscle Male	skeletal muscle
50	chr11:68291600-68294200	Enhancers	Fetal Heart	heart

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