Variant report

Variant	rs2281027
Chromosome Location	chr6:26446705-26446706
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:21)
CpG islands
(count:0)
Chromatin interactive
region (count:2)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:21 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	RELA	chr6:26446264-26446835	GM18505	blood:	n/a	n/a
2	FOXM1	chr6:26446080-26446846	GM12878	blood:	n/a	n/a
3	FOXM1	chr6:26446071-26446768	GM12878	blood:	n/a	n/a
4	EBF1	chr6:26446181-26446813	GM12878	blood:	n/a	n/a
5	IKZF1	chr6:26446135-26446857	GM12878	blood:	n/a	n/a
6	STAT5A	chr6:26446233-26446869	GM12878	blood:	n/a	n/a
7	MTA3	chr6:26446022-26446899	GM12878	blood:	n/a	n/a
8	IRF4	chr6:26445935-26446818	GM12878	blood:	n/a	n/a
9	NFIC	chr6:26445999-26446963	GM12878	blood:	n/a	n/a
10	ATF2	chr6:26446043-26446908	GM12878	blood:	n/a	n/a
11	BATF	chr6:26446083-26446930	GM12878	blood:	n/a	n/a
12	CEBPB	chr6:26446124-26446753	GM12878	blood:	n/a	n/a
13	RUNX3	chr6:26445926-26446894	GM12878	blood:	n/a	n/a
14	EP300	chr6:26446168-26446871	GM12878	blood:	n/a	n/a
15	CREB1	chr6:26446066-26446965	GM12878	blood:	n/a	n/a
16	RUNX3	chr6:26445900-26446936	GM12878	blood:	n/a	n/a
17	BATF	chr6:26446580-26446863	GM12878	blood:	n/a	n/a
18	MXI1	chr6:26446214-26446775	GM12878	blood:	n/a	n/a
19	ATF2	chr6:26446081-26446917	GM12878	blood:	n/a	n/a
20	RELA	chr6:26446273-26446810	GM19099	blood:	n/a	n/a
21	NFIC	chr6:26446070-26446904	GM12878	blood:	n/a	n/a

No data

(count:2 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr6:26445132..26448422-chr6:26449156..26450907,3	MCF-7	breast:
2	chr6:26440449..26443327-chr6:26444566..26448075,3	K562	blood:

No data

Variant related genes	Relation type
BTN3A3	TF binding region
ENSG00000111801	Chromatin interaction

Extended variants
information (count: 99 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:75)

rs_ID	r²[population]
rs1131936	1.00[JPT][hapmap]
rs11963680	1.00[ASN][1000 genomes]
rs11966630	0.89[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs12208788	1.00[JPT][hapmap]
rs13437008	1.00[ASN][1000 genomes]
rs13437012	1.00[ASN][1000 genomes]
rs13437351	1.00[CHB][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs13978	1.00[JPT][hapmap]
rs16891666	1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[YRI][hapmap];0.83[AFR][1000 genomes];0.83[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs1804836	0.83[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs2393650	0.89[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs3734541	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs3757140	0.89[YRI][hapmap]
rs3757141	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.89[ASN][1000 genomes]
rs3757147	1.00[JPT][hapmap]
rs3757149	0.89[MKK][hapmap];0.90[YRI][hapmap]
rs3846841	1.00[CHB][hapmap];1.00[JPT][hapmap];0.83[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs3846842	1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[YRI][hapmap];0.92[AFR][1000 genomes];0.91[AMR][1000 genomes];0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3857549	1.00[JPT][hapmap]
rs3885849	0.83[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs4422619	1.00[ASN][1000 genomes]
rs4476815	1.00[JPT][hapmap]
rs4712986	1.00[JPT][hapmap]
rs4712988	0.89[ASN][1000 genomes]
rs58380352	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs59121933	0.86[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs59621581	0.83[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs6456720	1.00[JPT][hapmap];0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs6456725	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs6456726	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs6456730	1.00[ASN][1000 genomes]
rs6901118	0.83[ASW][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.89[ASN][1000 genomes]
rs6902081	1.00[JPT][hapmap]
rs6907857	1.00[CHB][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs6910849	1.00[JPT][hapmap]
rs6910871	1.00[JPT][hapmap]
rs6910921	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs6910993	1.00[CHB][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs6911470	1.00[JPT][hapmap]
rs6911476	1.00[JPT][hapmap]
rs6929846	1.00[JPT][hapmap]
rs6935678	0.95[AFR][1000 genomes];0.89[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs6941018	1.00[ASN][1000 genomes]
rs72500814	0.89[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs7355	1.00[JPT][hapmap]
rs7356849	1.00[JPT][hapmap]
rs7356980	0.89[ASN][1000 genomes]
rs7356982	1.00[JPT][hapmap]
rs7751645	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.89[MEX][hapmap];1.00[TSI][hapmap];0.94[AFR][1000 genomes];0.91[AMR][1000 genomes];0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7769926	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs7773913	1.00[CHB][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs9104	1.00[JPT][hapmap]
rs9295692	1.00[JPT][hapmap]
rs9295700	1.00[JPT][hapmap]
rs9461247	0.83[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs9461249	0.80[LWK][hapmap];0.90[MKK][hapmap];0.90[YRI][hapmap]
rs9461252	1.00[ASW][hapmap];1.00[CHB][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.98[LWK][hapmap];0.99[MKK][hapmap];1.00[TSI][hapmap];0.96[YRI][hapmap];0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9461253	1.00[JPT][hapmap]
rs9461254	1.00[JPT][hapmap]
rs9461256	1.00[ASN][1000 genomes]
rs9467748	1.00[JPT][hapmap]
rs9467749	0.89[ASN][1000 genomes]
rs9467753	1.00[CHB][hapmap];1.00[JPT][hapmap];0.89[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs9467755	0.89[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs9467756	0.93[AFR][1000 genomes];0.89[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs9467757	1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9467759	1.00[JPT][hapmap]
rs9467760	0.85[JPT][hapmap]
rs9467761	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs9467765	1.00[ASN][1000 genomes]
rs9467768	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs9467769	1.00[ASN][1000 genomes]
rs9467771	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs9467788	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs9467803	1.00[JPT][hapmap]

Variant overlapped rSNPs/rCNVs (count:24 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1029920	chr6:25638507-26585842	Bivalent/Poised TSS Flanking Active TSS ZNF genes & repeats Enhancers Weak transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Active TSS Genic enhancers Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	1215 gene(s)	inside rSNPs	diseases
2	nsv538162	chr6:25638507-26585842	Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Weak transcription Strong transcription Enhancers 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 target site	1215 gene(s)	inside rSNPs	diseases
3	nsv1023453	chr6:25853830-26528250	Weak transcription Flanking Active TSS Enhancers Active TSS Bivalent/Poised TSS Strong transcription Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	1201 gene(s)	inside rSNPs	diseases
4	nsv482729	chr6:26291011-26470898	Weak transcription Active TSS Flanking Active TSS Enhancers Strong transcription Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	45 gene(s)	inside rSNPs	diseases
5	nsv482836	chr6:26352883-26520964	Enhancers Flanking Active TSS Strong transcription Active TSS Genic enhancers Weak transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	49 gene(s)	inside rSNPs	diseases
6	nsv482407	chr6:26369320-26550148	Active TSS Strong transcription Flanking Active TSS Weak transcription Genic enhancers ZNF genes & repeats Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	62 gene(s)	inside rSNPs	diseases
7	nsv883499	chr6:26377591-26454454	Enhancers Flanking Active TSS Genic enhancers Active TSS Weak transcription Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	28 gene(s)	inside rSNPs	diseases
8	esv3427999	chr6:26378373-26453532	Weak transcription Flanking Active TSS Strong transcription Enhancers Active TSS Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	28 gene(s)	inside rSNPs	diseases
9	nsv462664	chr6:26379537-26451553	Active TSS Weak transcription Flanking Active TSS Enhancers Strong transcription Genic enhancers 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 miRNA target site	27 gene(s)	inside rSNPs	diseases
10	nsv601184	chr6:26379537-26451553	Active TSS Genic enhancers Weak transcription Flanking Active TSS Enhancers Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	27 gene(s)	inside rSNPs	diseases
11	esv2763996	chr6:26423901-26465384	Enhancers Genic enhancers Weak transcription Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
12	nsv1017824	chr6:26425410-26465384	Strong transcription Active TSS Weak transcription Flanking Active TSS Enhancers 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 target site	16 gene(s)	inside rSNPs	diseases
13	nsv1030289	chr6:26428314-26464017	Weak transcription Strong transcription Active TSS Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
14	nsv1033003	chr6:26428314-26465384	Transcr. at gene 5' and 3' Strong transcription Enhancers Weak transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
15	nsv1031229	chr6:26428314-26467182	Active TSS Weak transcription Flanking Active TSS Enhancers Strong transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
16	nsv1031238	chr6:26428314-26471596	Strong transcription Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	17 gene(s)	inside rSNPs	diseases
17	nsv1024483	chr6:26429262-26465384	Flanking Active TSS Active TSS Strong transcription Enhancers Transcr. at gene 5' and 3' Weak transcription Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
18	nsv1034561	chr6:26429262-26467182	Enhancers Flanking Active TSS Strong transcription Active TSS Weak transcription Genic enhancers 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 target site	16 gene(s)	inside rSNPs	diseases
19	nsv528172	chr6:26430981-26463660	Genic enhancers Flanking Active TSS Enhancers Active TSS Weak transcription 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 target site	15 gene(s)	inside rSNPs	diseases
20	nsv1029357	chr6:26432815-26464789	Flanking Active TSS Enhancers Weak transcription Transcr. at gene 5' and 3' Active TSS Strong transcription Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	15 gene(s)	inside rSNPs	diseases
21	nsv1023581	chr6:26432815-26465384	Enhancers Weak transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS ZNF genes & repeats Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	15 gene(s)	inside rSNPs	diseases
22	nsv1024222	chr6:26432815-26467182	Strong transcription Enhancers Weak transcription Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	15 gene(s)	inside rSNPs	diseases
23	nsv1022309	chr6:26434914-26464789	Enhancers Strong transcription Active TSS Weak transcription Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	15 gene(s)	inside rSNPs	diseases
24	nsv969359	chr6:26443661-26453241	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	6 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:85 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:26441200-26449600	Weak transcription	Esophagus	oesophagus
2	chr6:26441200-26457000	Weak transcription	Brain Substantia Nigra	brain
3	chr6:26441200-26457600	Weak transcription	Pancreas	Pancrea
4	chr6:26441400-26448200	Weak transcription	Right Ventricle	heart
5	chr6:26441400-26453000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
6	chr6:26441400-26455600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
7	chr6:26441400-26457000	Weak transcription	Brain Anterior Caudate	brain
8	chr6:26441400-26457400	Weak transcription	Psoas Muscle	Psoas
9	chr6:26441600-26448000	Weak transcription	Placenta	Placenta
10	chr6:26441600-26448800	Weak transcription	Fetal Intestine Large	intestine
11	chr6:26441600-26451200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
12	chr6:26441600-26452400	Weak transcription	HSMMtube	muscle
13	chr6:26441600-26452800	Weak transcription	HSMM	muscle
14	chr6:26442200-26447000	Weak transcription	Fetal Intestine Small	intestine
15	chr6:26442200-26449200	Weak transcription	HUVEC	blood vessel
16	chr6:26442200-26455800	Weak transcription	HepG2	liver
17	chr6:26442200-26457400	Weak transcription	Fetal Kidney	kidney
18	chr6:26442400-26448000	Weak transcription	Primary hematopoietic stem cells	blood
19	chr6:26442400-26457400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
20	chr6:26442400-26457400	Weak transcription	Hela-S3	cervix
21	chr6:26442600-26450000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
22	chr6:26442600-26457400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
23	chr6:26442800-26454600	Weak transcription	NHDF-Ad	bronchial
24	chr6:26443000-26448400	Weak transcription	Colonic Mucosa	Colon
25	chr6:26443000-26450000	Weak transcription	Duodenum Smooth Muscle	Duodenum
26	chr6:26443000-26457400	Weak transcription	Stomach Mucosa	stomach
27	chr6:26444200-26448400	Genic enhancers	Primary T cells fromperipheralblood	blood
28	chr6:26444400-26447200	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
29	chr6:26444400-26447200	Genic enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
30	chr6:26444400-26447400	Strong transcription	Liver	Liver
31	chr6:26444400-26447800	Genic enhancers	Primary T helper cells PMA-I stimulated	--
32	chr6:26444400-26448000	Genic enhancers	Primary T helper memory cells from peripheral blood 2	blood
33	chr6:26444400-26448200	Genic enhancers	Primary T helper memory cells from peripheral blood 1	blood
34	chr6:26444400-26451000	Strong transcription	Fetal Muscle Trunk	muscle
35	chr6:26444400-26452000	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
36	chr6:26444400-26452600	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
37	chr6:26444400-26453000	Strong transcription	Fetal Stomach	stomach
38	chr6:26444600-26446800	Strong transcription	Rectal Mucosa Donor 29	rectum
39	chr6:26444600-26447000	Genic enhancers	Primary T cells from cord blood	blood
40	chr6:26444600-26447000	Genic enhancers	Primary mononuclear cells fromperipheralblood	Blood
41	chr6:26444600-26447400	Genic enhancers	Primary T helper cells fromperipheralblood	blood
42	chr6:26444600-26447600	Strong transcription	Fetal Lung	lung
43	chr6:26444600-26452000	Strong transcription	Fetal Muscle Leg	muscle
44	chr6:26444600-26453000	Strong transcription	Primary monocytes fromperipheralblood	blood
45	chr6:26444800-26447000	Strong transcription	Stomach Smooth Muscle	stomach
46	chr6:26444800-26447200	Genic enhancers	Fetal Thymus	thymus
47	chr6:26445000-26446800	Genic enhancers	Primary B cells from peripheral blood	blood
48	chr6:26445000-26449600	Weak transcription	Rectal Mucosa Donor 31	rectum
49	chr6:26445000-26454600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
50	chr6:26445200-26449600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin

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