Variant report

Variant	rs12281293
Chromosome Location	chr11:3963814-3963815
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	RUNX3	chr11:3963349-3964266	GM12878	blood:	n/a	n/a
2	CTCF	chr11:3963720-3963870	HepG2	liver:	n/a	chr11:3963810-3963828 chr11:3963811-3963827
3	TCF12	chr11:3963697-3964070	HepG2	liver:	n/a	chr11:3963933-3963940
4	HDAC2	chr11:3963687-3964166	HepG2	liver:	n/a	chr11:3963878-3963887
5	FOXA1	chr11:3963743-3964017	T-47D	breast:	n/a	chr11:3963873-3963888 chr11:3963889-3963904 chr11:3963875-3963887
6	CTCF	chr11:3963745-3963859	Pancreas_OC	pancreas:	n/a	chr11:3963810-3963828 chr11:3963811-3963827
7	RAD21	chr11:3963607-3964227	HepG2	liver:	n/a	n/a
8	MAZ	chr11:3963467-3963997	HepG2	liver:	n/a	n/a
9	CTCF	chr11:3963768-3963833	GM12892	blood:	n/a	chr11:3963810-3963828 chr11:3963811-3963827
10	FOXA1	chr11:3963727-3964024	T-47D	breast:	n/a	chr11:3963873-3963888 chr11:3963889-3963904 chr11:3963875-3963887
11	CTCF	chr11:3963752-3963857	GM19238	blood:	n/a	chr11:3963810-3963828 chr11:3963811-3963827
12	MYC	chr11:3963734-3963883	K562	blood:	n/a	n/a
13	RCOR1	chr11:3963662-3964032	K562	blood:	n/a	n/a
14	GATA3	chr11:3963722-3964080	T-47D	breast:	n/a	n/a
15	CUX1	chr11:3963773-3964020	K562	blood:	n/a	n/a
16	CTCF	chr11:3963740-3963890	HCPEpiC	choroid plexus:	n/a	chr11:3963810-3963828 chr11:3963811-3963827
17	RAD21	chr11:3963730-3963904	K562	blood:	n/a	n/a
18	STAT5A	chr11:3963404-3963853	GM12878	blood:	n/a	n/a
19	CTCF	chr11:3963740-3963890	K562	blood:	n/a	chr11:3963810-3963828 chr11:3963811-3963827
20	UBTF	chr11:3963783-3964024	K562	blood:	n/a	n/a
21	SMC3	chr11:3963648-3964328	HepG2	liver:	n/a	chr11:3963812-3963826
22	MYBL2	chr11:3963574-3964247	HepG2	liver:	n/a	n/a
23	TCF7L2	chr11:3963692-3964397	HepG2	liver:	n/a	n/a
24	HNF4G	chr11:3963709-3964211	HepG2	liver:	n/a	chr11:3964197-3964209
25	GATA3	chr11:3963753-3964086	T-47D	breast:	n/a	n/a
26	CTCF	chr11:3963737-3963875	Spleen_OC	spleen:	n/a	chr11:3963810-3963828 chr11:3963811-3963827
27	CTCF	chr11:3963684-3963955	HepG2	liver:	n/a	chr11:3963810-3963828 chr11:3963811-3963827
28	CTCF	chr11:3963752-3963872	Lung_OC	lung:	n/a	chr11:3963810-3963828 chr11:3963811-3963827
29	CTCF	chr11:3963680-3963830	HA-sp	spinal cord:	n/a	chr11:3963810-3963828 chr11:3963811-3963827
30	RAD21	chr11:3963595-3964060	HepG2	liver:	n/a	n/a
31	RUNX3	chr11:3963319-3964234	GM12878	blood:	n/a	n/a
32	FOXA1	chr11:3963621-3964116	HepG2	liver:	n/a	chr11:3963873-3963888 chr11:3963889-3963904 chr11:3963875-3963887
33	CTCF	chr11:3963702-3963931	HepG2	liver:	n/a	chr11:3963810-3963828 chr11:3963811-3963827
34	SMC3	chr11:3963714-3963874	K562	blood:	n/a	chr11:3963812-3963826
35	CTCF	chr11:3963644-3963999	K562	blood:	n/a	chr11:3963810-3963828 chr11:3963811-3963827
36	CTCF	chr11:3963720-3963870	GM12874	blood:	n/a	chr11:3963810-3963828 chr11:3963811-3963827
37	ZNF384	chr11:3963797-3963824	K562	blood:	n/a	n/a
38	HCFC1	chr11:3963806-3963883	K562	blood:	n/a	n/a
39	RAD21	chr11:3963727-3963887	K562	blood:	n/a	n/a
40	SP1	chr11:3963688-3964154	HepG2	liver:	n/a	n/a
41	ZNF143	chr11:3963768-3963900	K562	blood:	n/a	n/a
42	FOXA1	chr11:3963558-3964239	HepG2	liver:	n/a	chr11:3963873-3963888 chr11:3963889-3963904 chr11:3963875-3963887
43	TCF7L2	chr11:3963760-3964129	PANC-1	pancreas:	n/a	n/a
44	NFIC	chr11:3963419-3964144	GM12878	blood:	n/a	n/a
45	HNF4A	chr11:3963704-3964378	HepG2	liver:	n/a	chr11:3964197-3964209
46	CHD2	chr11:3963662-3963835	HepG2	liver:	n/a	n/a
47	TEAD4	chr11:3963621-3964235	HepG2	liver:	n/a	n/a
48	FOXA2	chr11:3963632-3964271	HepG2	liver:	n/a	chr11:3963875-3963887
49	HNF4A	chr11:3963714-3964083	HepG2	liver:	n/a	n/a
50	CTCF	chr11:3963700-3963941	K562	blood:	n/a	chr11:3963810-3963828 chr11:3963811-3963827

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr11:3963150..3965730-chr11:3971154..3972718,2	K562	blood:
2	chr11:3959785..3962625-chr11:3963394..3965455,2	K562	blood:

Variant related genes	Relation type
STIM1	TF binding region

Extended variants
information (count: 98 )
Associated
traits (count: 3 )

rSNPs within LD-proxies of this variant (count:90)

rs_ID	r²[population]
rs1013351	1.00[CHB][hapmap];0.88[JPT][hapmap];1.00[YRI][hapmap];0.84[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs10500590	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs10742200	0.86[EUR][1000 genomes]
rs10767702	1.00[CHB][hapmap];0.86[JPT][hapmap];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs10767713	0.83[AMR][1000 genomes];0.94[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs10767715	1.00[CHB][hapmap];0.87[JPT][hapmap];1.00[YRI][hapmap];0.84[AFR][1000 genomes];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs10767723	0.81[EUR][1000 genomes]
rs10767767	1.00[CHB][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];0.93[AMR][1000 genomes];0.89[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs10767811	0.90[CHB][hapmap];0.87[JPT][hapmap]
rs10835311	1.00[CHB][hapmap];0.88[JPT][hapmap];1.00[YRI][hapmap];0.84[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs10835312	0.84[AFR][1000 genomes];0.95[AMR][1000 genomes];0.96[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs10835324	0.81[EUR][1000 genomes]
rs10835331	1.00[CHB][hapmap];0.88[JPT][hapmap];0.88[AMR][1000 genomes];0.96[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs10835333	0.81[EUR][1000 genomes]
rs10835337	0.87[EUR][1000 genomes]
rs10835340	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs10835359	0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10835390	0.87[EUR][1000 genomes]
rs10835399	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10835402	1.00[CHB][hapmap];0.88[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10835403	1.00[CHB][hapmap];0.87[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10835406	1.00[CHB][hapmap];0.88[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10835407	1.00[CHB][hapmap];0.87[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10835454	0.87[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs10835474	0.88[AMR][1000 genomes];0.90[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs10835508	0.90[CHB][hapmap];0.88[JPT][hapmap];0.86[EUR][1000 genomes]
rs10835521	0.90[CHB][hapmap];0.88[JPT][hapmap];1.00[YRI][hapmap]
rs10835540	0.90[CHB][hapmap];0.86[JPT][hapmap]
rs10835556	0.90[CHB][hapmap];0.86[JPT][hapmap];1.00[YRI][hapmap];0.84[AFR][1000 genomes];0.85[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs10835557	0.84[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs10835561	0.90[CHB][hapmap];0.88[JPT][hapmap];1.00[YRI][hapmap];0.84[AFR][1000 genomes]
rs10835596	0.90[CHB][hapmap];0.87[JPT][hapmap];1.00[YRI][hapmap];0.83[EUR][1000 genomes]
rs10835597	0.81[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs10835601	0.90[CHB][hapmap];0.88[JPT][hapmap];1.00[YRI][hapmap];0.87[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs10835604	0.90[CHB][hapmap];0.88[JPT][hapmap];0.80[AMR][1000 genomes]
rs11030276	1.00[CHB][hapmap];0.86[JPT][hapmap];1.00[YRI][hapmap];0.84[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs11030404	0.87[EUR][1000 genomes]
rs11030579	0.88[AMR][1000 genomes];0.88[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs11030599	0.84[AMR][1000 genomes];0.91[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs11030627	0.84[AMR][1000 genomes];0.87[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs11030631	0.84[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs11030639	0.90[CHB][hapmap];0.87[JPT][hapmap];0.86[EUR][1000 genomes]
rs11030660	0.86[JPT][hapmap];0.87[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs11030781	0.90[CHB][hapmap];0.87[JPT][hapmap]
rs11493482	0.88[AMR][1000 genomes];0.91[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs11828337	0.85[EUR][1000 genomes]
rs12223176	1.00[CHB][hapmap];0.87[JPT][hapmap];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12283447	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12286710	1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs12290747	0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs12295138	0.87[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs1349583	1.00[CHB][hapmap];0.87[JPT][hapmap];0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1442726	0.90[CHB][hapmap];0.88[JPT][hapmap];0.81[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs1452047	1.00[CHB][hapmap];0.87[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1452048	0.88[EUR][1000 genomes]
rs17081	1.00[CHB][hapmap];0.87[JPT][hapmap];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs17279635	1.00[CHB][hapmap];0.87[JPT][hapmap];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1839910	0.88[EUR][1000 genomes]
rs2119987	0.80[EUR][1000 genomes]
rs2412338	0.87[EUR][1000 genomes]
rs28419002	1.00[AFR][1000 genomes]
rs2898947	1.00[CHB][hapmap];0.88[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4910590	0.88[AMR][1000 genomes];0.88[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs4910596	0.84[AFR][1000 genomes];0.85[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs4910597	0.84[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs4910598	0.83[EUR][1000 genomes]
rs4910866	1.00[CHB][hapmap];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs4910868	1.00[CHB][hapmap];0.88[JPT][hapmap];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4910869	1.00[CHB][hapmap];0.86[JPT][hapmap];0.94[AMR][1000 genomes];0.92[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs4910875	0.88[JPT][hapmap];1.00[YRI][hapmap];0.85[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs4910877	0.90[CHB][hapmap];0.88[JPT][hapmap]
rs4910880	0.90[CHB][hapmap];0.88[JPT][hapmap];1.00[YRI][hapmap];0.84[AFR][1000 genomes]
rs6578424	0.87[EUR][1000 genomes]
rs66503725	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs66596383	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs67065286	0.85[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs67300156	0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7102215	1.00[CHB][hapmap];0.88[JPT][hapmap];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs7113845	0.86[EUR][1000 genomes]
rs7128762	1.00[CHB][hapmap];0.88[JPT][hapmap];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs714380	0.83[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs71466139	0.81[AMR][1000 genomes];0.81[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs718937	1.00[YRI][hapmap]
rs720571	1.00[CHB][hapmap];0.87[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];0.96[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7924984	0.87[EUR][1000 genomes]
rs7925954	0.83[EUR][1000 genomes]
rs7935824	0.88[JPT][hapmap];0.88[EUR][1000 genomes]
rs7950153	1.00[CHB][hapmap];0.87[JPT][hapmap];0.83[AMR][1000 genomes];0.95[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs963998	0.90[CHB][hapmap];0.87[JPT][hapmap]
rs995498	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1049560	chr11:3678259-3980746	Weak transcription Genic enhancers Enhancers Flanking Active TSS Strong transcription Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	32 gene(s)	inside rSNPs	diseases
2	nsv540907	chr11:3678259-3980746	Weak transcription Active TSS Enhancers Genic enhancers Strong transcription Flanking 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	32 gene(s)	inside rSNPs	diseases
3	nsv1052744	chr11:3739162-4017601	Weak transcription Enhancers Active TSS Flanking Active TSS Strong transcription 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	29 gene(s)	inside rSNPs	diseases
4	nsv1047025	chr11:3750969-4017601	Strong transcription Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	28 gene(s)	inside rSNPs	diseases
5	nsv1046065	chr11:3808818-4049150	Active TSS Weak transcription Enhancers Genic enhancers Flanking Active TSS Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	29 gene(s)	inside rSNPs	diseases
6	nsv540909	chr11:3808818-4049150	Flanking Active TSS Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	29 gene(s)	inside rSNPs	diseases
7	nsv869701	chr11:3879297-3973762	Enhancers Genic enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Strong transcription ZNF genes & repeats Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	8 gene(s)	inside rSNPs	diseases
8	nsv896895	chr11:3942001-3972236	Enhancers Strong transcription Weak transcription Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases

mRNA abundance (count:3)

SNP	Gene	Cis/trans	Tissue	Source
rs12281293	RRM1	cis	Thyroid	GTEx
rs12281293	RRM1	cis	Artery Tibial	GTEx
rs12281293	STIM1	cis	lung	GTEx

Chromatin state (count:95 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:3950400-3972200	Weak transcription	Fetal Muscle Trunk	muscle
2	chr11:3951200-3965400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
3	chr11:3951200-3967600	Weak transcription	Brain Inferior Temporal Lobe	brain
4	chr11:3956200-3964000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
5	chr11:3958800-3968000	Enhancers	Primary T killer naive cells fromperipheralblood	blood
6	chr11:3960000-3967600	Enhancers	Skeletal Muscle Male	skeletal muscle
7	chr11:3960200-3967600	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
8	chr11:3961000-3964200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
9	chr11:3961200-3964600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
10	chr11:3961200-4002000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
11	chr11:3961400-3964400	Enhancers	Right Atrium	heart
12	chr11:3961400-3964800	Weak transcription	Cortex derived primary cultured neurospheres	brain
13	chr11:3961400-3965200	Enhancers	Sigmoid Colon	Sigmoid Colon
14	chr11:3961400-3968600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
15	chr11:3961400-3968600	Enhancers	Skeletal Muscle Female	skeletal muscle
16	chr11:3961400-3969200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
17	chr11:3961600-3966400	Enhancers	NHDF-Ad	bronchial
18	chr11:3961600-3967600	Weak transcription	Brain Angular Gyrus	brain
19	chr11:3961600-3967800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
20	chr11:3961600-3968000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
21	chr11:3961600-3968400	Weak transcription	NHEK	skin
22	chr11:3961600-3975200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
23	chr11:3961800-3964000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
24	chr11:3961800-3965600	Weak transcription	NHLF	lung
25	chr11:3961800-3968000	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
26	chr11:3962000-3965200	Weak transcription	Placenta Amnion	Placenta Amnion
27	chr11:3962000-3971800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
28	chr11:3962000-3973400	Weak transcription	Ovary	ovary
29	chr11:3962400-3964000	Enhancers	Thymus	Thymus
30	chr11:3962400-3968000	Enhancers	Primary T helper naive cells fromperipheralblood	blood
31	chr11:3962400-3968400	Enhancers	Primary T regulatory cells fromperipheralblood	blood
32	chr11:3962600-3968200	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
33	chr11:3963000-3964000	Enhancers	Primary T cells fromperipheralblood	blood
34	chr11:3963000-3964800	Enhancers	Right Ventricle	heart
35	chr11:3963000-3966400	Enhancers	Psoas Muscle	Psoas
36	chr11:3963000-3967000	Enhancers	Fetal Thymus	thymus
37	chr11:3963000-3968600	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
38	chr11:3963000-3973200	Enhancers	Primary B cells from peripheral blood	blood
39	chr11:3963200-3964400	Flanking Active TSS	GM12878-XiMat	blood
40	chr11:3963200-3964800	Enhancers	Rectal Mucosa Donor 31	rectum
41	chr11:3963200-3965400	Enhancers	Liver	Liver
42	chr11:3963200-3967800	Enhancers	Primary hematopoietic stem cells short term culture	blood
43	chr11:3963200-3968400	Enhancers	Primary hematopoietic stem cells	blood
44	chr11:3963400-3964000	Genic enhancers	Esophagus	oesophagus
45	chr11:3963400-3964200	Enhancers	Placenta	Placenta
46	chr11:3963400-3964200	Enhancers	Pancreas	Pancrea
47	chr11:3963400-3964400	Flanking Active TSS	Primary T helper 17 cells PMA-I stimulated	--
48	chr11:3963400-3964400	Enhancers	Aorta	Aorta
49	chr11:3963400-3964400	Enhancers	Lung	lung
50	chr11:3963400-3964400	Enhancers	A549	lung

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