Variant report

Variant	rs1771482
Chromosome Location	chr1:228412106-228412107
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr1:228412002..228414034-chr1:228460124..228463067,2	K562	blood:
2	chr1:228404999..228407013-chr1:228410390..228412165,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000269890	Chromatin interaction

Extended variants
information (count: 129 )
Associated
traits (count: 6 )

rSNPs within LD-proxies of this variant (count:118)

rs_ID	r²[population]
rs10158357	0.84[CEU][hapmap];0.91[MEX][hapmap];0.86[TSI][hapmap]
rs1059778	1.00[CEU][hapmap];0.81[CHB][hapmap];0.95[GIH][hapmap];0.83[TSI][hapmap];0.83[EUR][1000 genomes]
rs10753445	1.00[CEU][hapmap];0.87[GIH][hapmap];0.83[TSI][hapmap];0.83[EUR][1000 genomes]
rs10799468	0.80[EUR][1000 genomes]
rs10799471	0.93[EUR][1000 genomes]
rs10916265	0.88[CEU][hapmap]
rs10916268	0.83[ASW][hapmap];0.92[CEU][hapmap];0.90[GIH][hapmap];0.81[LWK][hapmap];0.86[TSI][hapmap];0.81[EUR][1000 genomes]
rs10916271	0.83[EUR][1000 genomes]
rs11580411	0.84[EUR][1000 genomes]
rs11584385	1.00[CEU][hapmap];0.93[TSI][hapmap];0.97[EUR][1000 genomes]
rs11799681	0.93[EUR][1000 genomes]
rs11804508	0.94[EUR][1000 genomes]
rs12024649	0.93[EUR][1000 genomes]
rs12084338	0.84[CEU][hapmap]
rs12118872	0.91[CEU][hapmap];0.82[EUR][1000 genomes]
rs12130630	0.84[CEU][hapmap]
rs12564763	0.88[ASW][hapmap];0.88[CEU][hapmap];0.90[GIH][hapmap];0.83[LWK][hapmap];0.86[TSI][hapmap]
rs12726781	0.94[EUR][1000 genomes]
rs12745416	1.00[CEU][hapmap];0.94[EUR][1000 genomes]
rs1331303	0.93[AFR][1000 genomes];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1411910	1.00[CEU][hapmap];0.93[TSI][hapmap];0.97[EUR][1000 genomes]
rs1411911	0.85[EUR][1000 genomes]
rs1411913	0.85[EUR][1000 genomes]
rs1557026	0.84[CEU][hapmap]
rs1620111	1.00[CEU][hapmap];0.90[TSI][hapmap];0.94[EUR][1000 genomes]
rs1629290	0.83[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs1629294	0.94[ASW][hapmap];1.00[CEU][hapmap];0.95[CHB][hapmap];0.89[CHD][hapmap];0.97[GIH][hapmap];0.94[JPT][hapmap];1.00[LWK][hapmap];0.87[MEX][hapmap];1.00[MKK][hapmap];0.97[TSI][hapmap];1.00[YRI][hapmap];0.99[AFR][1000 genomes];0.86[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1757129	0.97[EUR][1000 genomes]
rs1757132	1.00[CEU][hapmap];0.86[CHB][hapmap];0.96[YRI][hapmap];0.98[AFR][1000 genomes];0.83[AMR][1000 genomes];0.98[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs1757133	1.00[CEU][hapmap];0.96[EUR][1000 genomes]
rs1757138	0.81[AMR][1000 genomes];0.97[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs1757139	0.94[ASW][hapmap];1.00[CEU][hapmap];0.87[GIH][hapmap];0.98[LWK][hapmap];0.96[MEX][hapmap];1.00[MKK][hapmap];0.97[TSI][hapmap];0.93[YRI][hapmap];0.93[AFR][1000 genomes];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs1757140	0.96[EUR][1000 genomes]
rs1757141	0.96[EUR][1000 genomes]
rs1757142	0.90[AFR][1000 genomes];0.93[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs1757144	0.99[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1757145	0.97[EUR][1000 genomes]
rs1757147	1.00[CEU][hapmap];0.90[CHB][hapmap];0.94[JPT][hapmap];0.96[YRI][hapmap];0.99[AFR][1000 genomes];0.85[AMR][1000 genomes];0.99[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs1757148	0.94[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1757149	0.94[ASW][hapmap];1.00[CEU][hapmap];0.90[CHB][hapmap];0.85[CHD][hapmap];0.95[GIH][hapmap];0.94[JPT][hapmap];1.00[LWK][hapmap];0.97[TSI][hapmap];1.00[YRI][hapmap];0.98[AFR][1000 genomes];0.87[AMR][1000 genomes];0.99[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs1757150	1.00[CEU][hapmap];0.90[CHB][hapmap];0.94[JPT][hapmap];0.96[YRI][hapmap];0.99[AFR][1000 genomes];0.87[AMR][1000 genomes];0.99[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs1757151	0.98[EUR][1000 genomes]
rs1757152	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];0.97[TSI][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1757155	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1757156	1.00[ASW][hapmap];1.00[CEU][hapmap];0.95[CHB][hapmap];0.89[CHD][hapmap];0.97[GIH][hapmap];0.94[JPT][hapmap];0.98[LWK][hapmap];1.00[MKK][hapmap];0.97[TSI][hapmap];0.89[YRI][hapmap];0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1757158	0.81[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs17640616	0.84[CEU][hapmap];0.88[TSI][hapmap];0.86[EUR][1000 genomes]
rs1771459	1.00[CEU][hapmap];0.86[CHB][hapmap];0.90[GIH][hapmap];0.81[AMR][1000 genomes];0.98[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs1771460	1.00[ASW][hapmap];1.00[CEU][hapmap];0.90[GIH][hapmap];0.98[LWK][hapmap];0.96[MEX][hapmap];0.98[MKK][hapmap];0.97[TSI][hapmap];0.93[YRI][hapmap];0.93[AFR][1000 genomes];0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs1771461	1.00[CEU][hapmap];0.97[EUR][1000 genomes]
rs1771462	1.00[CEU][hapmap];0.90[CHB][hapmap];0.82[JPT][hapmap];0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1771467	1.00[CEU][hapmap];0.86[CHB][hapmap];0.96[YRI][hapmap];0.98[AFR][1000 genomes];0.83[AMR][1000 genomes];0.98[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs1771468	0.95[AFR][1000 genomes];0.96[EUR][1000 genomes]
rs1771469	0.98[AFR][1000 genomes];0.83[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs1771470	0.89[AFR][1000 genomes];0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs1771471	0.96[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1771472	1.00[CEU][hapmap];0.84[YRI][hapmap];0.94[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1771474	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.97[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];0.91[MEX][hapmap];1.00[MKK][hapmap];0.97[TSI][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1771476	1.00[CEU][hapmap];0.90[CHB][hapmap];0.94[JPT][hapmap];0.96[YRI][hapmap];0.99[AFR][1000 genomes];0.85[AMR][1000 genomes];0.99[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs1771477	0.85[AMR][1000 genomes];0.99[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs1771478	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1771479	1.00[CEU][hapmap];0.90[CHB][hapmap];0.94[JPT][hapmap];0.96[YRI][hapmap];0.99[AFR][1000 genomes];0.87[AMR][1000 genomes];0.99[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs1771483	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[YRI][hapmap];1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1771484	0.96[CEU][hapmap];0.97[EUR][1000 genomes]
rs1771485	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.89[YRI][hapmap];0.92[AFR][1000 genomes];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1771487	0.96[CEU][hapmap];0.90[TSI][hapmap];0.92[EUR][1000 genomes]
rs2066237	0.88[ASW][hapmap];1.00[CEU][hapmap];0.81[CHB][hapmap];0.95[GIH][hapmap];0.81[LWK][hapmap];0.83[TSI][hapmap]
rs2185544	0.84[EUR][1000 genomes]
rs2313601	1.00[CEU][hapmap];0.90[TSI][hapmap];0.94[EUR][1000 genomes]
rs2313602	0.88[ASW][hapmap];1.00[CEU][hapmap];0.90[GIH][hapmap];0.83[LWK][hapmap];0.86[TSI][hapmap];0.81[EUR][1000 genomes]
rs2776845	0.99[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2776853	0.94[EUR][1000 genomes]
rs2776855	1.00[CEU][hapmap];0.93[TSI][hapmap];0.96[EUR][1000 genomes]
rs2776856	1.00[ASW][hapmap];1.00[CEU][hapmap];0.90[GIH][hapmap];0.98[LWK][hapmap];0.91[MEX][hapmap];1.00[MKK][hapmap];0.97[TSI][hapmap];0.93[YRI][hapmap];0.91[AFR][1000 genomes];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs2792984	0.95[EUR][1000 genomes]
rs2872538	1.00[CEU][hapmap];0.93[TSI][hapmap];0.97[EUR][1000 genomes]
rs2989563	0.85[EUR][1000 genomes]
rs3121188	0.84[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs3121190	0.86[EUR][1000 genomes]
rs3121191	0.90[EUR][1000 genomes]
rs3121192	0.92[EUR][1000 genomes]
rs3795777	0.97[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs3795782	0.92[CEU][hapmap];0.87[MEX][hapmap];0.85[TSI][hapmap];0.84[EUR][1000 genomes]
rs4653536	0.81[EUR][1000 genomes]
rs4653543	0.95[EUR][1000 genomes]
rs4653545	0.92[EUR][1000 genomes]
rs4653915	0.88[CEU][hapmap]
rs4653917	0.84[CEU][hapmap]
rs4653921	0.84[CEU][hapmap]
rs4653931	0.96[EUR][1000 genomes]
rs4653933	0.94[EUR][1000 genomes]
rs4653934	0.83[EUR][1000 genomes]
rs489926	0.90[EUR][1000 genomes]
rs491293	0.92[EUR][1000 genomes]
rs493945	0.96[CEU][hapmap];0.93[TSI][hapmap];0.82[EUR][1000 genomes]
rs512406	0.86[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs545313	0.91[EUR][1000 genomes]
rs546967	0.91[EUR][1000 genomes]
rs55658545	0.86[EUR][1000 genomes]
rs55971985	0.94[EUR][1000 genomes]
rs56112646	0.98[AFR][1000 genomes];0.83[AMR][1000 genomes];0.98[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs56168609	0.81[EUR][1000 genomes]
rs566640	0.92[EUR][1000 genomes]
rs61825279	0.81[EUR][1000 genomes]
rs61827540	0.96[EUR][1000 genomes]
rs6426492	0.81[CEU][hapmap]
rs6657968	0.84[CEU][hapmap]
rs6661539	0.86[EUR][1000 genomes]
rs6673893	0.84[CEU][hapmap]
rs6682260	0.84[CEU][hapmap]
rs72757829	0.83[EUR][1000 genomes]
rs7512209	0.88[ASW][hapmap];1.00[CEU][hapmap];0.90[GIH][hapmap];0.86[TSI][hapmap]
rs7525075	0.85[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs7532141	0.82[EUR][1000 genomes]
rs7532924	1.00[CEU][hapmap];0.86[CHB][hapmap];0.81[JPT][hapmap];0.80[AMR][1000 genomes];0.87[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs7537636	1.00[CEU][hapmap];0.90[GIH][hapmap];0.86[TSI][hapmap]
rs7539762	0.84[CEU][hapmap]
rs947087	1.00[CEU][hapmap];0.83[MEX][hapmap];0.93[TSI][hapmap];0.81[AMR][1000 genomes];0.97[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:11 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv32853	chr1:227880116-228806209	Enhancers Genic enhancers Bivalent Enhancer Weak transcription Flanking Bivalent TSS/Enh Strong transcription Active TSS Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	187 gene(s)	inside rSNPs	diseases
2	nsv826908	chr1:227895386-228691100	Strong transcription Enhancers Flanking Active TSS Bivalent/Poised TSS Weak transcription Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	157 gene(s)	inside rSNPs	diseases
3	nsv523935	chr1:228038124-228681749	Enhancers Flanking Active TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Strong transcription Weak transcription Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	137 gene(s)	inside rSNPs	diseases
4	nsv873253	chr1:228231601-228537942	Flanking Active TSS Weak transcription Enhancers ZNF genes & repeats Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Strong transcription Transcr. at gene 5' and 3' Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	91 gene(s)	inside rSNPs	diseases
5	nsv873254	chr1:228231601-228543800	Weak transcription Genic enhancers Active TSS Enhancers Flanking Active TSS Strong transcription Bivalent Enhancer ZNF genes & repeats 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	91 gene(s)	inside rSNPs	diseases
6	nsv873255	chr1:228254753-228684779	Genic enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Strong transcription Enhancers Active TSS 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	133 gene(s)	inside rSNPs	diseases
7	nsv827019	chr1:228314167-228651020	Enhancers Weak transcription Genic enhancers Active TSS Flanking Active TSS Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	106 gene(s)	inside rSNPs	diseases
8	nsv873257	chr1:228322826-228412106	Genic enhancers Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Weak transcription Strong transcription Enhancers Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	66 gene(s)	inside rSNPs	diseases
9	nsv1012078	chr1:228340876-228521843	Weak transcription Genic enhancers Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Strong transcription Enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	63 gene(s)	inside rSNPs	diseases
10	nsv535320	chr1:228340876-228521843	Active TSS Enhancers Bivalent Enhancer Weak transcription Strong transcription Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	63 gene(s)	inside rSNPs	diseases
11	nsv873263	chr1:228391808-228494790	Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer Active TSS ZNF genes & repeats Strong transcription Weak transcription Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	22 gene(s)	inside rSNPs	diseases

mRNA abundance (count:6)

SNP	Gene	Cis/trans	Tissue	Source
rs1771482	WDR26	cis	cerebellum	SCAN
rs1771482	MRPL55	cis	parietal	SCAN
rs1771482	OBSCN	cis	Skin Sun Exposed Lower leg	GTEx
rs1771482	MRPL55	cis	cerebellum	SCAN
rs1771482	IBA57	cis	Whole Blood	GTEx
rs1771482	OBSCN	cis	Esophagus Mucosa	GTEx

Chromatin state (count:94 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:228401400-228412200	Weak transcription	HSMMtube	muscle
2	chr1:228401400-228412600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
3	chr1:228401600-228412200	Weak transcription	Right Atrium	heart
4	chr1:228402000-228412200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
5	chr1:228402000-228412200	Weak transcription	Duodenum Mucosa	Duodenum
6	chr1:228402000-228412600	Weak transcription	Fetal Kidney	kidney
7	chr1:228402200-228412200	Weak transcription	A549	lung
8	chr1:228402200-228412200	Weak transcription	Hela-S3	cervix
9	chr1:228402200-228412200	Weak transcription	NHEK	skin
10	chr1:228402200-228412400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
11	chr1:228402200-228412600	Weak transcription	Primary B cells from cord blood	blood
12	chr1:228402200-228415200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
13	chr1:228402200-228425800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
14	chr1:228402200-228428800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
15	chr1:228402400-228412400	Weak transcription	Rectal Mucosa Donor 29	rectum
16	chr1:228402400-228412600	Weak transcription	HMEC	breast
17	chr1:228402600-228418000	Strong transcription	Primary T cells from cord blood	blood
18	chr1:228402800-228412600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
19	chr1:228403000-228412200	Strong transcription	HUES64 Cell Line	embryonic stem cell
20	chr1:228403000-228412200	Weak transcription	Colonic Mucosa	Colon
21	chr1:228403000-228428200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
22	chr1:228403200-228418000	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
23	chr1:228403400-228415000	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
24	chr1:228404200-228412200	Weak transcription	Brain Hippocampus Middle	brain
25	chr1:228404200-228412600	Weak transcription	Fetal Brain Male	brain
26	chr1:228407600-228412200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
27	chr1:228407600-228412200	Weak transcription	Sigmoid Colon	Sigmoid Colon
28	chr1:228408000-228412200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
29	chr1:228408200-228412200	Weak transcription	Primary T helper cells PMA-I stimulated	--
30	chr1:228408200-228412200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
31	chr1:228408200-228412200	Weak transcription	Psoas Muscle	Psoas
32	chr1:228408600-228412200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
33	chr1:228408600-228412400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
34	chr1:228410000-228416600	Strong transcription	H9 Cell Line	embryonic stem cell
35	chr1:228410200-228412200	Strong transcription	HUES6 Cell Line	embryonic stem cell
36	chr1:228410200-228412200	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
37	chr1:228410200-228413600	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
38	chr1:228410200-228414800	Transcr. at gene 5' and 3'	Skeletal Muscle Male	skeletal muscle
39	chr1:228410400-228412400	Strong transcription	Fetal Muscle Trunk	muscle
40	chr1:228410400-228412600	Strong transcription	Fetal Lung	lung
41	chr1:228410400-228412800	ZNF genes & repeats	Aorta	Aorta
42	chr1:228410400-228415600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
43	chr1:228410600-228416400	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
44	chr1:228410800-228413000	ZNF genes & repeats	Primary T helper naive cells fromperipheralblood	blood
45	chr1:228410800-228416800	Strong transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
46	chr1:228411000-228413200	ZNF genes & repeats	Breast Myoepithelial Primary Cells	Breast
47	chr1:228411000-228415000	Weak transcription	Small Intestine	intestine
48	chr1:228411200-228412200	Strong transcription	Right Ventricle	heart
49	chr1:228411400-228413400	ZNF genes & repeats	Fetal Intestine Small	intestine
50	chr1:228411400-228413600	ZNF genes & repeats	IMR90 fetal lung fibroblasts Cell Line	lung

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