Variant report

Variant	rs613973
Chromosome Location	chr11:85460909-85460910
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:0)
CpG islands
(count:0)
Chromatin interactive
region (count:11)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:11 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:85457148..85461266-chr11:85520193..85525185,6	MCF-7	breast:
2	chr11:85434439..85436977-chr11:85459317..85462236,2	MCF-7	breast:
3	chr11:85459647..85464805-chr11:85466382..85469125,4	K562	blood:
4	chr11:85459647..85463395-chr11:85466382..85468116,3	K562	blood:
5	chr11:85456348..85458453-chr11:85459854..85462602,2	K562	blood:
6	chr11:85456923..85462918-chr11:85517727..85523482,9	MCF-7	breast:
7	chr11:85456897..85461654-chr11:85539528..85543738,6	MCF-7	breast:
8	chr11:85459682..85462503-chr11:85466829..85468700,3	MCF-7	breast:
9	chr11:85460295..85462125-chr11:85496572..85498601,2	MCF-7	breast:
10	chr11:85456354..85459698-chr11:85460209..85463531,4	MCF-7	breast:
11	chr11:85457955..85460944-chr11:85541331..85543778,2	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000137501	Chromatin interaction

Extended variants
information (count: 114 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:81)

rs_ID	r²[population]
rs10501595	0.86[CHB][hapmap];1.00[JPT][hapmap]
rs11234410	0.81[ASN][1000 genomes]
rs1151152	0.92[AMR][1000 genomes];0.92[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs11604141	0.80[CHB][hapmap];0.81[ASN][1000 genomes]
rs11604178	0.81[ASN][1000 genomes]
rs1192	0.86[CHB][hapmap];0.92[JPT][hapmap]
rs1214001	0.87[CHB][hapmap];0.92[JPT][hapmap]
rs12419172	1.00[JPT][hapmap]
rs12792050	0.91[AMR][1000 genomes];0.86[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs1445513	0.81[CHB][hapmap];0.81[ASN][1000 genomes]
rs17208492	0.87[CHB][hapmap];1.00[JPT][hapmap]
rs17208519	0.87[CHB][hapmap];1.00[JPT][hapmap]
rs17810659	0.87[CHB][hapmap];1.00[JPT][hapmap]
rs188311	0.87[CEU][hapmap];0.93[CHB][hapmap];1.00[JPT][hapmap]
rs1892872	1.00[JPT][hapmap]
rs1991923	1.00[JPT][hapmap]
rs2290823	0.87[CHB][hapmap];1.00[JPT][hapmap]
rs2467059	0.87[CHB][hapmap];1.00[JPT][hapmap]
rs290175	0.88[CEU][hapmap];0.93[CHB][hapmap];1.00[JPT][hapmap]
rs290177	0.87[CHB][hapmap];1.00[JPT][hapmap]
rs290182	0.87[CHB][hapmap];1.00[JPT][hapmap]
rs290186	0.87[CHB][hapmap];1.00[JPT][hapmap]
rs290190	0.84[CEU][hapmap]
rs290194	0.92[CEU][hapmap];0.93[CHB][hapmap];1.00[JPT][hapmap]
rs290195	0.92[CEU][hapmap]
rs290196	0.88[CEU][hapmap];0.93[CHB][hapmap];1.00[JPT][hapmap]
rs290199	0.91[CEU][hapmap];0.87[CHB][hapmap];1.00[JPT][hapmap]
rs290200	0.83[CEU][hapmap]
rs290202	0.84[CEU][hapmap]
rs487964	0.84[ASN][1000 genomes]
rs489896	0.81[AFR][1000 genomes];0.84[ASN][1000 genomes]
rs491867	0.87[CEU][hapmap]
rs493673	0.89[ASN][1000 genomes]
rs4943925	0.82[CHB][hapmap];1.00[JPT][hapmap]
rs4944529	0.87[CHB][hapmap];1.00[JPT][hapmap]
rs4944531	0.87[CHB][hapmap];1.00[JPT][hapmap]
rs496187	0.87[CEU][hapmap]
rs510948	0.87[CEU][hapmap];0.87[CHB][hapmap];0.92[JPT][hapmap];0.89[ASN][1000 genomes]
rs520629	0.91[CEU][hapmap];0.82[ASN][1000 genomes]
rs521764	0.82[ASN][1000 genomes]
rs537266	0.91[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.85[ASN][1000 genomes]
rs537604	0.87[CEU][hapmap];0.87[CHB][hapmap];0.92[JPT][hapmap];0.89[ASN][1000 genomes]
rs540063	0.91[CEU][hapmap]
rs543995	0.82[ASN][1000 genomes]
rs550404	0.83[CEU][hapmap];1.00[YRI][hapmap];0.90[AFR][1000 genomes]
rs556669	0.84[CEU][hapmap]
rs558377	0.84[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs565494	0.91[AMR][1000 genomes];0.82[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs56579	0.87[CHB][hapmap];1.00[JPT][hapmap]
rs573766	0.88[CEU][hapmap];0.93[CHB][hapmap];1.00[JPT][hapmap];0.84[YRI][hapmap]
rs578324	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.84[YRI][hapmap];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs580459	0.83[CEU][hapmap]
rs583122	0.95[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs589327	0.92[CEU][hapmap]
rs592380	0.84[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs592712	0.96[CEU][hapmap];0.87[CHB][hapmap];0.92[JPT][hapmap];0.87[YRI][hapmap];0.92[AMR][1000 genomes];0.90[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs597480	0.88[CEU][hapmap]
rs609012	1.00[CEU][hapmap];0.86[CHB][hapmap];0.92[JPT][hapmap];0.87[YRI][hapmap];0.97[AMR][1000 genomes];0.93[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs631104	0.89[ASN][1000 genomes]
rs631410	0.96[CEU][hapmap]
rs639688	0.95[CEU][hapmap];0.80[CHB][hapmap];0.92[JPT][hapmap];0.83[ASN][1000 genomes]
rs640620	0.82[ASN][1000 genomes]
rs641393	0.88[CEU][hapmap]
rs644558	0.91[AMR][1000 genomes];0.85[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs644972	0.96[CEU][hapmap]
rs647912	0.96[CEU][hapmap]
rs650036	1.00[CEU][hapmap];0.93[CHB][hapmap];1.00[JPT][hapmap];0.87[YRI][hapmap];0.95[AMR][1000 genomes];0.88[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs650970	0.90[ASN][1000 genomes]
rs653559	0.96[CEU][hapmap];0.93[CHB][hapmap];1.00[JPT][hapmap];0.85[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs666176	0.94[AMR][1000 genomes];0.93[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs679204	0.92[CEU][hapmap]
rs680498	0.87[CEU][hapmap]
rs681044	1.00[CEU][hapmap];0.93[CHB][hapmap];0.93[JPT][hapmap];0.89[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs683903	0.80[ASN][1000 genomes]
rs688741	1.00[CEU][hapmap];0.93[CHB][hapmap];1.00[JPT][hapmap];0.84[YRI][hapmap];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7119617	0.87[CHB][hapmap];0.92[JPT][hapmap]
rs7943586	0.87[CHB][hapmap];1.00[JPT][hapmap]
rs7948778	0.80[CHB][hapmap]
rs881121	0.86[CHB][hapmap];1.00[JPT][hapmap]
rs947861	0.87[CHB][hapmap];1.00[JPT][hapmap]
rs947863	0.87[CHB][hapmap];1.00[JPT][hapmap]

Variant overlapped rSNPs/rCNVs (count:33 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1051155	chr11:85006564-85721261	Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	64 gene(s)	inside rSNPs	diseases
2	nsv541110	chr11:85006564-85721261	Enhancers Strong transcription Weak transcription Bivalent Enhancer ZNF genes & repeats Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	64 gene(s)	inside rSNPs	diseases
3	esv2758279	chr11:85180480-85603988	Flanking Active TSS Active TSS Weak transcription Enhancers Genic enhancers Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	56 gene(s)	inside rSNPs	diseases
4	esv2759845	chr11:85180480-85603988	Flanking Active TSS Weak transcription Enhancers Genic enhancers Active TSS ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	56 gene(s)	inside rSNPs	diseases
5	nsv832222	chr11:85405712-85603981	Enhancers Active TSS Bivalent Enhancer Weak transcription Strong transcription ZNF genes & repeats Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
6	nsv898050	chr11:85406915-85499290	Enhancers Weak transcription Flanking Active TSS Strong transcription Genic enhancers Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
7	nsv1052123	chr11:85425856-85471132	Enhancers Genic enhancers Weak transcription Active TSS Strong transcription Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
8	nsv555633	chr11:85426330-85473883	Weak transcription Enhancers Active TSS Genic enhancers Flanking Active TSS Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
9	nsv1036110	chr11:85429074-85471132	Enhancers Active TSS Weak transcription Strong transcription Flanking Active TSS Bivalent Enhancer Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
10	nsv1054027	chr11:85429074-85477283	Weak transcription Enhancers Transcr. at gene 5' and 3' Genic enhancers Flanking Active TSS Bivalent Enhancer Active TSS Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
11	esv3471508	chr11:85429687-85472395	Active TSS Enhancers Strong transcription Flanking Active TSS Weak transcription Genic enhancers Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
12	esv3471519	chr11:85429687-85472395	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Active TSS Strong transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
13	nsv555634	chr11:85430397-85464922	Enhancers Strong transcription Weak transcription Flanking Active TSS Genic enhancers Active TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
14	nsv555635	chr11:85430397-85470893	Weak transcription Genic enhancers Enhancers Flanking Active TSS Strong transcription Active TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
15	nsv555636	chr11:85431886-85465179	Strong transcription Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Genic enhancers ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
16	nsv1042192	chr11:85433687-85464922	Enhancers Flanking Active TSS Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Bivalent Enhancer Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
17	nsv1039118	chr11:85433687-85468605	Flanking Active TSS Weak transcription Strong transcription Enhancers Genic enhancers Bivalent Enhancer Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
18	nsv1039830	chr11:85433687-85470589	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
19	nsv1047001	chr11:85433687-85470941	Enhancers Weak transcription Genic enhancers Flanking Active TSS Bivalent Enhancer Strong transcription Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
20	nsv1042942	chr11:85433687-85471132	Enhancers Weak transcription Flanking Active TSS Strong transcription Bivalent Enhancer Genic enhancers ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
21	nsv1052732	chr11:85434057-85468605	Weak transcription Strong transcription Enhancers Flanking Active TSS Active TSS Bivalent Enhancer Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
22	nsv1048844	chr11:85434057-85470941	Enhancers Weak transcription Flanking Active TSS Strong transcription Genic enhancers ZNF genes & repeats Bivalent Enhancer Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
23	nsv1051644	chr11:85434057-85471132	Genic enhancers Weak transcription Flanking Active TSS Enhancers Strong transcription Bivalent Enhancer ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
24	nsv555637	chr11:85435730-85470893	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
25	nsv555639	chr11:85436352-85495269	Enhancers Flanking Active TSS Weak transcription Genic enhancers ZNF genes & repeats Active TSS Bivalent Enhancer Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
26	nsv1048750	chr11:85436840-85471132	Enhancers Genic enhancers Active TSS Strong transcription Weak transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
27	esv2754674	chr11:85436852-85470852	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS Bivalent Enhancer Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
28	esv2757459	chr11:85436868-85473347	Weak transcription Enhancers Flanking Active TSS Strong transcription Genic enhancers Bivalent Enhancer Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
29	nsv541112	chr11:85436956-85468985	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
30	nsv541113	chr11:85437155-85468845	Genic enhancers Enhancers Flanking Active TSS Weak transcription Strong transcription Bivalent Enhancer Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
31	nsv555640	chr11:85456703-85464922	Enhancers Strong transcription Bivalent Enhancer Weak transcription Flanking Active TSS Genic enhancers Active TSS	Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
32	nsv1047147	chr11:85459235-85594800	Flanking Active TSS Active TSS Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
33	nsv541114	chr11:85459235-85594800	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs613973	SYTL2	cis	Muscle Skeletal	GTEx

Chromatin state (count:78 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:85430400-85480400	Weak transcription	Aorta	Aorta
2	chr11:85431800-85466600	Weak transcription	Brain Substantia Nigra	brain
3	chr11:85442200-85461000	Weak transcription	Brain Cingulate Gyrus	brain
4	chr11:85444400-85461600	Weak transcription	Lung	lung
5	chr11:85448000-85463600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
6	chr11:85448000-85480600	Weak transcription	Fetal Stomach	stomach
7	chr11:85449200-85478400	Weak transcription	Right Ventricle	heart
8	chr11:85452000-85462600	Weak transcription	HSMMtube	muscle
9	chr11:85452400-85461800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
10	chr11:85452800-85463000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
11	chr11:85453000-85471000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
12	chr11:85454200-85461000	Weak transcription	Fetal Lung	lung
13	chr11:85454200-85462600	Weak transcription	Left Ventricle	heart
14	chr11:85455000-85470800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
15	chr11:85455800-85461800	Enhancers	Stomach Mucosa	stomach
16	chr11:85456800-85468600	Weak transcription	Psoas Muscle	Psoas
17	chr11:85457000-85461400	Weak transcription	Spleen	Spleen
18	chr11:85457000-85462600	Weak transcription	Pancreas	Pancrea
19	chr11:85457000-85469000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
20	chr11:85457000-85469000	Weak transcription	Gastric	stomach
21	chr11:85457400-85466400	Weak transcription	Colonic Mucosa	Colon
22	chr11:85457600-85466400	Weak transcription	Fetal Intestine Small	intestine
23	chr11:85457800-85461400	Weak transcription	Sigmoid Colon	Sigmoid Colon
24	chr11:85457800-85466400	Weak transcription	Fetal Intestine Large	intestine
25	chr11:85458600-85461600	Enhancers	H1 Cell Line	embryonic stem cell
26	chr11:85458800-85461400	Strong transcription	Rectal Mucosa Donor 31	rectum
27	chr11:85459000-85461600	Enhancers	A549	lung
28	chr11:85459000-85462000	Enhancers	H9 Cell Line	embryonic stem cell
29	chr11:85459200-85461600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
30	chr11:85459200-85462000	Enhancers	ES-I3 Cell Line	embryonic stem cell
31	chr11:85459200-85462000	Enhancers	iPS-15b Cell Line	embryonic stem cell
32	chr11:85459200-85462000	Enhancers	Osteobl	bone
33	chr11:85459200-85462200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
34	chr11:85459200-85463400	Weak transcription	Rectal Mucosa Donor 29	rectum
35	chr11:85459400-85461000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
36	chr11:85459400-85461200	Enhancers	HUES64 Cell Line	embryonic stem cell
37	chr11:85459400-85461200	Enhancers	iPS-18 Cell Line	embryonic stem cell
38	chr11:85459400-85461600	Enhancers	HUES6 Cell Line	embryonic stem cell
39	chr11:85459400-85470600	Weak transcription	HSMM	muscle
40	chr11:85459800-85461000	Enhancers	Primary T helper cells PMA-I stimulated	--
41	chr11:85459800-85470600	Weak transcription	NHEK	skin
42	chr11:85460000-85461800	Enhancers	iPS-20b Cell Line	embryonic stem cell
43	chr11:85460000-85465200	Enhancers	Primary hematopoietic stem cells	blood
44	chr11:85460200-85461000	Weak transcription	NH-A	brain
45	chr11:85460200-85462000	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
46	chr11:85460200-85463000	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
47	chr11:85460200-85463000	Enhancers	Primary T helper cells fromperipheralblood	blood
48	chr11:85460200-85463400	Enhancers	Primary T killer naive cells fromperipheralblood	blood
49	chr11:85460400-85461000	Enhancers	ES-WA7 Cell Line	embryonic stem cell
50	chr11:85460400-85461000	Enhancers	Small Intestine	intestine

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links