Variant report

Variant	rs2276014
Chromosome Location	chr11:64081445-64081446
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:13)
CpG islands
(count:61)
Chromatin interactive
region (count:11)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:13 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	POLR2A	chr11:64080095-64085877	K562	blood:	n/a	n/a
2	POLR2A	chr11:64081138-64081469	U87	brain:	n/a	n/a
3	POLR2A	chr11:64081391-64086324	GM12892	blood:	n/a	n/a
4	POLR2A	chr11:64081037-64082394	HL-60	blood:	n/a	n/a
5	POLR2A	chr11:64081371-64081768	GM12878	blood:	n/a	n/a
6	POLR2A	chr11:64081348-64081785	GM12878	blood:	n/a	n/a
7	POLR2A	chr11:64081122-64086449	HepG2	liver:	n/a	n/a
8	POLR2A	chr11:64080947-64081633	U87	brain:	n/a	n/a
9	POLR2A	chr11:64081029-64084143	K562	blood:	n/a	n/a
10	CTCF	chr11:64081360-64081510	AoAF	blood vessel:	n/a	n/a
11	POLR2A	chr11:64081143-64086133	SK-N-MC	brain:	n/a	n/a
12	POLR2A	chr11:64081441-64081445	Hela-S3	cervix:	n/a	n/a
13	POLR2A	chr11:64081027-64081627	U87	brain:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:64081430-64081480	HCPEpiC	choroid plexus:	n/a
2	chr11:64081430-64081480	NT2-D1	testis:	n/a
3	chr11:64081430-64081480	Caco-2	colon:	n/a
4	chr11:64081430-64081480	NB4	blood:	n/a
5	chr11:64081430-64081480	GM12892	blood:	n/a
6	chr11:64081430-64081480	HL-60	blood:	n/a
7	chr11:64081430-64081480	HEEpiC	esophagus:	n/a
8	chr11:64081430-64081480	GM12891	blood:	n/a
9	chr11:64081430-64081480	NHDF-neo	bronchial:	n/a
10	chr11:64081430-64081480	GM06990	blood:	n/a
11	chr11:64081430-64081480	HCT-116	colon:	n/a
12	chr11:64081430-64081480	HCM	heart:	n/a
13	chr11:64081430-64081480	AG09309	skin:	n/a
14	chr11:64081430-64081480	LNCaP	prostate:	n/a
15	chr11:64081430-64081480	U87	brain:	n/a
16	chr11:64081430-64081480	HPAEpiC	pulmonary alveolar:	n/a
17	chr11:64081430-64081480	MCF10A-Er-Src	breast:	n/a
18	chr11:64081430-64081480	AG10803	skin:	n/a
19	chr11:64081430-64081480	GM19239	blood:	n/a
20	chr11:64081430-64081480	NHBE	bronchial:	n/a
21	chr11:64081430-64081480	HMEC	breast:	n/a
22	chr11:64081430-64081480	AG04450	lung:	fetal
23	chr11:64081430-64081480	Hela-S3	cervix:	n/a
24	chr11:64081430-64081480	ECC-1	luminal epithelium:	n/a
25	chr11:64081430-64081480	HRPEpiC	eye:	n/a
26	chr11:64081430-64081480	PFSK-1	brain:	n/a
27	chr11:64081430-64081480	T-47D	breast:	n/a
28	chr11:64081430-64081480	AG09319	gingival:	n/a
29	chr11:64081430-64081480	SK-N-SH	brain:	n/a
30	chr11:64081430-64081480	HRCEpiC	kidney:	n/a
31	chr11:64081430-64081480	SKMC	muscle:	n/a
32	chr11:64081430-64081480	AoSMC	blood vessel:	n/a
33	chr11:64081430-64081480	NH-A	brain:	n/a
34	chr11:64081430-64081480	Jurkat	blood:	n/a
35	chr11:64081430-64081480	ProgFib	skin:	n/a
36	chr11:64081430-64081480	GM12878	blood:	n/a
37	chr11:64081430-64081480	HAEpiC	amniotic membrane:	n/a
38	chr11:64081430-64081480	HUVEC	blood vessel:	n/a
39	chr11:64081430-64081480	BJ	skin:	n/a
40	chr11:64081430-64081480	HIPEpiC	eye:	n/a
41	chr11:64081430-64081480	Hepatocyte	liver:	n/a
42	chr11:64081430-64081480	SK-N-SH_RA	brain:	n/a
43	chr11:64081430-64081480	HCF	heart:	n/a
44	chr11:64081430-64081480	MCF-7	breast:	n/a
45	chr11:64081430-64081480	RPTEC	kidney:	n/a
46	chr11:64081430-64081480	HEK293	kidney:	embryo
47	chr11:64081430-64081480	HRE	kidney:	n/a
48	chr11:64081430-64081480	H1-hESC	embryonic stem cell:	embryo
49	chr11:64081430-64081480	ovcar-3	ovarian:	n/a
50	chr11:64081430-64081480	PrEC	prostate:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr11:64078839..64083408-chr11:64108257..64111409,4	MCF-7	breast:
2	chr11:63969363..63977705-chr11:64080619..64088284,16	K562	blood:
3	chr11:64050229..64053074-chr11:64081177..64083173,2	MCF-7	breast:
4	chr11:64058435..64061008-chr11:64080225..64081908,2	K562	blood:
5	chr11:64081246..64082787-chr11:64121396..64124105,2	K562	blood:
6	chr11:64080620..64083894-chr11:64124180..64128334,3	MCF-7	breast:
7	chr11:63998837..64000808-chr11:64079142..64081596,2	MCF-7	breast:
8	chr11:63991810..63993878-chr11:64081220..64083594,2	K562	blood:
9	chr11:64033536..64040775-chr11:64080684..64088458,16	K562	blood:
10	chr11:63952189..63953757-chr11:64081280..64082901,2	K562	blood:
11	chr11:64050061..64052819-chr11:64080707..64082589,2	MCF-7	breast:

No data

Variant related genes	Relation type
ESRRA	TF binding region
PRDX5	TF binding region
PRDX5	CpG island
ESRRA	CpG island
ENSG00000173264	Chromatin interaction
ENSG00000182450	Chromatin interaction
ENSG00000149743	Chromatin interaction
ENSG00000257069	Chromatin interaction
ENSG00000002330	Chromatin interaction
ENSG00000168071	Chromatin interaction
ENSG00000149781	Chromatin interaction
ENSG00000162302	Chromatin interaction
ENSG00000168439	Chromatin interaction
ENSG00000149761	Chromatin interaction
ENSG00000110011	Chromatin interaction

Extended variants
information (count: 48 )
Associated
traits (count: 3 )

rSNPs within LD-proxies of this variant (count:24)

rs_ID	r²[population]
rs1047206	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11600990	0.92[CEU][hapmap];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];1.00[ASN][1000 genomes]
rs11606014	0.88[AMR][1000 genomes];0.85[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs12785488	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12788266	1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12793347	0.82[AFR][1000 genomes];0.83[AMR][1000 genomes];0.86[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs12798408	0.83[AMR][1000 genomes];0.82[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs12808002	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2286614	1.00[CHB][hapmap];1.00[YRI][hapmap];0.82[AFR][1000 genomes];0.93[AMR][1000 genomes];0.95[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2289573	0.81[AMR][1000 genomes]
rs28395875	0.81[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs28395876	0.86[ASN][1000 genomes]
rs34292685	0.92[CEU][hapmap];0.82[CHB][hapmap];0.93[AMR][1000 genomes];0.94[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs34906890	0.83[AMR][1000 genomes]
rs35692796	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs41294396	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs477895	0.92[CEU][hapmap];0.92[EUR][1000 genomes]
rs66968227	0.82[AFR][1000 genomes];0.93[AMR][1000 genomes];0.95[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs71456304	1.00[AMR][1000 genomes];0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs71456309	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs71456310	0.81[AMR][1000 genomes]
rs7938380	0.88[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs7939107	0.88[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs7947143	0.92[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]

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	nsv897631	chr11:63664882-64129722	Flanking Active TSS Strong transcription Enhancers Weak transcription Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	254 gene(s)	inside rSNPs	diseases
2	esv1802079	chr11:63746066-64151373	Bivalent Enhancer Flanking Active TSS Weak transcription Enhancers Genic enhancers Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	247 gene(s)	inside rSNPs	diseases
3	nsv897646	chr11:63754986-64150370	Strong transcription Weak transcription Bivalent Enhancer Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Active TSS Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	245 gene(s)	inside rSNPs	diseases
4	nsv1035875	chr11:63800238-64132030	Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Active TSS Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	234 gene(s)	inside rSNPs	diseases
5	nsv469961	chr11:63822940-64085967	Weak transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Enhancers Active TSS Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	224 gene(s)	inside rSNPs	diseases
6	nsv897660	chr11:63860826-64125142	Weak transcription Active TSS Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	231 gene(s)	inside rSNPs	diseases
7	nsv897661	chr11:63863405-64129722	Flanking Active TSS Enhancers Weak transcription Active TSS Bivalent/Poised TSS Strong transcription Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	233 gene(s)	inside rSNPs	diseases
8	nsv897662	chr11:63889749-64150370	Flanking Active TSS Enhancers Weak transcription Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Active TSS Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	237 gene(s)	inside rSNPs	diseases
9	nsv897664	chr11:63919742-64150370	Weak transcription Strong transcription Flanking Active TSS Enhancers Genic enhancers Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	237 gene(s)	inside rSNPs	diseases
10	nsv869944	chr11:63932152-64123062	Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers Active TSS 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 miRNA target site	227 gene(s)	inside rSNPs	diseases
11	nsv468593	chr11:63941734-64089874	Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Enhancers Genic enhancers Strong transcription Weak transcription Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	212 gene(s)	inside rSNPs	diseases
12	nsv555185	chr11:63941734-64089874	Weak transcription Enhancers Active TSS Flanking Active TSS Genic enhancers Bivalent Enhancer Strong transcription 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	212 gene(s)	inside rSNPs	diseases
13	nsv555186	chr11:63949095-64097233	Weak transcription Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Strong transcription Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	212 gene(s)	inside rSNPs	diseases
14	nsv897668	chr11:63964657-64085298	Weak transcription Genic enhancers Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Enhancers Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	163 gene(s)	inside rSNPs	diseases
15	nsv897669	chr11:63964657-64089874	Genic enhancers Weak transcription Strong transcription Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	164 gene(s)	inside rSNPs	diseases
16	nsv897670	chr11:63964657-64097233	Flanking Active TSS Weak transcription Active TSS Enhancers Strong transcription Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	164 gene(s)	inside rSNPs	diseases
17	nsv897671	chr11:63964657-64150370	Active TSS Flanking Active TSS Genic enhancers Weak transcription Enhancers Strong transcription Bivalent Enhancer 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 miRNA target site	179 gene(s)	inside rSNPs	diseases
18	nsv832186	chr11:63972260-64170059	Active TSS Genic enhancers Weak transcription Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	180 gene(s)	inside rSNPs	diseases
19	nsv897672	chr11:63979643-64082807	Enhancers Flanking Active TSS Genic enhancers Bivalent Enhancer Weak transcription Strong transcription Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	140 gene(s)	inside rSNPs	diseases
20	esv1802320	chr11:63987425-64154633	Active TSS Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Weak transcription Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	178 gene(s)	inside rSNPs	diseases
21	nsv897679	chr11:63994692-64150370	Enhancers Weak transcription Active TSS Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	169 gene(s)	inside rSNPs	diseases
22	nsv897682	chr11:63999529-64170500	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS Genic enhancers Transcr. at gene 5' and 3' Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	164 gene(s)	inside rSNPs	diseases
23	nsv1043277	chr11:64002997-64132030	Bivalent/Poised TSS Enhancers Active TSS Flanking Active TSS Weak transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	157 gene(s)	inside rSNPs	diseases
24	nsv897685	chr11:64048912-64150370	Strong transcription Bivalent Enhancer Weak transcription Flanking Active TSS Enhancers Genic enhancers Transcr. at gene 5' and 3' Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	102 gene(s)	inside rSNPs	diseases

mRNA abundance (count:3)

SNP	Gene	Cis/trans	Tissue	Source
rs2276014	TEX40	cis	Thyroid	GTEx
rs2276014	TRPT1	cis	Muscle Skeletal	GTEx
rs2276014	PPP1R14B	Cis_1M	lymphoblastoid	RTeQTL

Chromatin state (count:125 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:64074000-64084400	Weak transcription	Aorta	Aorta
2	chr11:64074200-64084400	Weak transcription	Ovary	ovary
3	chr11:64074400-64084200	Weak transcription	Pancreatic Islets	Pancreatic Islet
4	chr11:64074600-64081800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
5	chr11:64074600-64081800	Weak transcription	Colon Smooth Muscle	Colon
6	chr11:64074600-64081800	Weak transcription	Fetal Lung	lung
7	chr11:64074600-64081800	Weak transcription	NH-A	brain
8	chr11:64074600-64082000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
9	chr11:64074600-64083800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
10	chr11:64074600-64083800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
11	chr11:64074600-64083800	Weak transcription	HUVEC	blood vessel
12	chr11:64074600-64084000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
13	chr11:64074600-64084200	Weak transcription	Fetal Kidney	kidney
14	chr11:64074800-64081800	Weak transcription	HUES64 Cell Line	embryonic stem cell
15	chr11:64074800-64081800	Weak transcription	Primary hematopoietic stem cells	blood
16	chr11:64074800-64081800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
17	chr11:64074800-64081800	Weak transcription	Duodenum Smooth Muscle	Duodenum
18	chr11:64074800-64082000	Weak transcription	Brain Hippocampus Middle	brain
19	chr11:64074800-64082200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
20	chr11:64074800-64083600	Weak transcription	Osteobl	bone
21	chr11:64074800-64084000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
22	chr11:64074800-64084600	Weak transcription	Small Intestine	intestine
23	chr11:64075000-64081600	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
24	chr11:64075000-64081800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
25	chr11:64075000-64081800	Weak transcription	Primary B cells from cord blood	blood
26	chr11:64075000-64083600	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
27	chr11:64075000-64084000	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
28	chr11:64075000-64084200	Weak transcription	Fetal Brain Male	brain
29	chr11:64075200-64081600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
30	chr11:64075200-64081800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
31	chr11:64075200-64081800	Weak transcription	Placenta Amnion	Placenta Amnion
32	chr11:64075200-64082000	Weak transcription	Brain Cingulate Gyrus	brain
33	chr11:64075200-64082200	Weak transcription	Brain Angular Gyrus	brain
34	chr11:64075200-64082600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
35	chr11:64075200-64083600	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
36	chr11:64075200-64083800	Weak transcription	Fetal Heart	heart
37	chr11:64075200-64084200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
38	chr11:64075200-64084200	Weak transcription	Psoas Muscle	Psoas
39	chr11:64075600-64081800	Weak transcription	Brain Anterior Caudate	brain
40	chr11:64075600-64084000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
41	chr11:64075800-64081600	Weak transcription	Primary T cells from cord blood	blood
42	chr11:64075800-64081800	Weak transcription	HUES48 Cell Line	embryonic stem cell
43	chr11:64078200-64082000	Enhancers	Breast Myoepithelial Primary Cells	Breast
44	chr11:64078400-64083200	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
45	chr11:64078400-64083400	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
46	chr11:64078400-64083600	Strong transcription	Primary neutrophils fromperipheralblood	blood
47	chr11:64078400-64084000	Strong transcription	Fetal Stomach	stomach
48	chr11:64078400-64084000	Strong transcription	Sigmoid Colon	Sigmoid Colon
49	chr11:64078800-64081600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
50	chr11:64078800-64082600	Strong transcription	Fetal Intestine Small	intestine

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