Variant report

Variant	rs2073818
Chromosome Location	chr9:136918662-136918663
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr9:136904281..136909955-chr9:136916883..136922324,6	MCF-7	breast:
2	chr9:136917576..136919094-chr9:136919756..136922437,2	K562	blood:
3	chr9:136913228..136917389-chr9:136917645..136921079,5	K562	blood:

Variant related genes	Relation type
ENSG00000169925	Chromatin interaction

Extended variants
information (count: 90 )
Associated
traits (count: 5 )

rSNPs within LD-proxies of this variant (count:64)

rs_ID	r²[population]
rs1079524	0.91[JPT][hapmap];0.82[ASN][1000 genomes]
rs109536	0.93[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs10993894	0.84[EUR][1000 genomes]
rs10993895	0.91[CEU][hapmap];0.84[CHB][hapmap];0.95[CHD][hapmap];0.86[GIH][hapmap];1.00[JPT][hapmap];0.97[TSI][hapmap];0.93[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs1124317	0.94[CHB][hapmap];0.88[CHD][hapmap];1.00[JPT][hapmap];0.89[ASN][1000 genomes]
rs2106223	1.00[JPT][hapmap]
rs2157770	0.94[CHB][hapmap];1.00[JPT][hapmap];0.92[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2427946	0.85[ASN][1000 genomes]
rs2427949	0.86[ASN][1000 genomes]
rs2427951	0.86[ASN][1000 genomes]
rs2427977	0.81[ASN][1000 genomes]
rs2506699	0.85[ASN][1000 genomes]
rs2506700	0.85[ASN][1000 genomes]
rs2506713	0.82[ASN][1000 genomes]
rs2506714	0.82[ASN][1000 genomes]
rs2519078	0.94[CHB][hapmap];1.00[JPT][hapmap];0.85[ASN][1000 genomes]
rs2519080	0.95[JPT][hapmap]
rs2519081	0.94[CHB][hapmap];1.00[JPT][hapmap];0.89[ASN][1000 genomes]
rs2519831	0.93[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2520094	1.00[ASW][hapmap];0.91[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.98[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];0.89[MEX][hapmap];1.00[MKK][hapmap];0.97[TSI][hapmap];0.87[YRI][hapmap];0.97[AFR][1000 genomes];0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2520095	0.95[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2520096	0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2520099	0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2810480	0.87[ASN][1000 genomes]
rs2810489	1.00[CEU][hapmap];0.89[CHB][hapmap];0.93[CHD][hapmap];0.89[GIH][hapmap];0.91[JPT][hapmap];1.00[TSI][hapmap];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2810490	0.83[CEU][hapmap];0.84[AMR][1000 genomes]
rs2810491	1.00[CEU][hapmap];1.00[CHB][hapmap];0.95[CHD][hapmap];0.89[GIH][hapmap];0.91[JPT][hapmap];0.85[MEX][hapmap];0.91[TSI][hapmap];0.89[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs3004622	0.82[ASN][1000 genomes]
rs3094339	0.84[EUR][1000 genomes]
rs378740	0.92[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs379417	0.95[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs379471	0.83[EUR][1000 genomes]
rs386770	0.93[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs392134	0.90[AMR][1000 genomes];0.99[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs401826	0.81[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs408307	1.00[CEU][hapmap];0.84[CHB][hapmap];0.97[CHD][hapmap];0.89[GIH][hapmap];1.00[JPT][hapmap];0.97[TSI][hapmap];0.93[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs410876	1.00[CEU][hapmap];0.84[CHB][hapmap];0.97[CHD][hapmap];0.89[GIH][hapmap];0.95[JPT][hapmap];0.94[TSI][hapmap];0.93[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs416390	1.00[CEU][hapmap];0.84[CHB][hapmap];0.97[CHD][hapmap];0.93[GIH][hapmap];1.00[JPT][hapmap];0.84[MEX][hapmap];0.82[MKK][hapmap];1.00[TSI][hapmap];0.90[AMR][1000 genomes];0.99[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs433402	0.95[CEU][hapmap];0.84[CHB][hapmap];1.00[JPT][hapmap];0.94[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs437182	0.89[ASN][1000 genomes]
rs443876	0.84[CHB][hapmap];0.90[CHD][hapmap];1.00[JPT][hapmap];0.82[ASN][1000 genomes]
rs448918	0.92[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs455073	0.90[AMR][1000 genomes];0.99[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs455381	1.00[CEU][hapmap];0.84[CHB][hapmap];1.00[JPT][hapmap];0.95[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs456205	0.90[AMR][1000 genomes];0.99[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs456207	0.97[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs456793	0.87[ASN][1000 genomes]
rs457420	0.94[CHB][hapmap];0.93[CHD][hapmap];0.89[GIH][hapmap];1.00[JPT][hapmap];0.84[ASN][1000 genomes]
rs459571	0.95[CEU][hapmap];0.94[CHB][hapmap];1.00[JPT][hapmap];0.87[AMR][1000 genomes];0.99[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs460154	1.00[CEU][hapmap];0.94[CHB][hapmap];0.95[CHD][hapmap];0.98[GIH][hapmap];1.00[JPT][hapmap];0.97[TSI][hapmap];0.98[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs460888	0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs461462	0.98[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs464024	0.80[ASN][1000 genomes]
rs464826	0.94[CHB][hapmap];0.92[CHD][hapmap];0.95[JPT][hapmap];0.80[ASN][1000 genomes]
rs465535	0.95[CEU][hapmap];0.89[CHB][hapmap];1.00[JPT][hapmap];0.98[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs465724	1.00[CEU][hapmap];0.94[CHB][hapmap];1.00[CHD][hapmap];0.98[GIH][hapmap];1.00[JPT][hapmap];0.97[TSI][hapmap];0.97[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs466681	0.91[EUR][1000 genomes]
rs467303	0.95[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs467379	0.84[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs467387	0.87[AMR][1000 genomes];0.94[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs482481	0.82[EUR][1000 genomes]
rs55923934	0.93[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs736902	0.80[CHD][hapmap];0.91[JPT][hapmap];0.82[ASN][1000 genomes]
rs756679	0.91[JPT][hapmap]

Variant overlapped rSNPs/rCNVs (count:26 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv894125	chr9:136723520-136931957	Enhancers Strong transcription Weak transcription Flanking Active TSS Active TSS Genic enhancers 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 target site	31 gene(s)	inside rSNPs	diseases
2	nsv831748	chr9:136788484-136944326	Genic enhancers Weak transcription Enhancers Strong transcription Flanking Active TSS Bivalent Enhancer Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	30 gene(s)	inside rSNPs	diseases
3	nsv894132	chr9:136813341-136950691	Active TSS Genic enhancers Weak transcription Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	28 gene(s)	inside rSNPs	diseases
4	nsv428226	chr9:136825035-136994606	Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Weak transcription Strong transcription Active TSS Genic enhancers Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	28 gene(s)	inside rSNPs	diseases
5	nsv894135	chr9:136839840-136927657	Strong transcription Enhancers Genic enhancers Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats 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	23 gene(s)	inside rSNPs	diseases
6	nsv894136	chr9:136839840-136938961	Flanking Active TSS Active TSS Enhancers Bivalent Enhancer Strong transcription Weak transcription ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	27 gene(s)	inside rSNPs	diseases
7	nsv894137	chr9:136839840-136950691	Weak transcription Enhancers Active TSS Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	28 gene(s)	inside rSNPs	diseases
8	nsv894138	chr9:136839840-137093168	Strong transcription Genic enhancers Enhancers Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	34 gene(s)	inside rSNPs	diseases
9	nsv825148	chr9:136848471-137025632	Flanking Bivalent TSS/Enh Active TSS Strong transcription Weak transcription Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	31 gene(s)	inside rSNPs	diseases
10	nsv894139	chr9:136863932-136950691	Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Weak transcription ZNF genes & repeats Enhancers Active TSS Strong transcription 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
11	nsv894140	chr9:136865879-136927657	Enhancers ZNF genes & repeats Weak transcription Strong transcription Active TSS Genic enhancers Bivalent Enhancer Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	12 gene(s)	inside rSNPs	diseases
12	nsv894141	chr9:136865879-136938961	Active TSS Weak transcription Flanking Active TSS Strong transcription Enhancers Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
13	nsv466627	chr9:136870787-136938961	Enhancers Flanking Active TSS Genic enhancers Weak transcription Strong transcription 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 target site	16 gene(s)	inside rSNPs	diseases
14	nsv615774	chr9:136870787-136938961	Flanking Active TSS Enhancers Bivalent Enhancer Weak transcription Genic enhancers Flanking Bivalent TSS/Enh Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
15	nsv1048571	chr9:136872166-137265444	Weak transcription Strong transcription Enhancers Active TSS Flanking Active TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	50 gene(s)	inside rSNPs	diseases
16	nsv894145	chr9:136874066-136925451	Flanking Active TSS Enhancers ZNF genes & repeats Weak transcription Genic enhancers Active TSS Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	12 gene(s)	inside rSNPs	diseases
17	nsv894146	chr9:136874066-136938961	Strong transcription Enhancers Active TSS Flanking Active TSS Weak transcription Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
18	nsv894147	chr9:136874066-136950691	Enhancers Genic enhancers Strong transcription Active TSS Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	17 gene(s)	inside rSNPs	diseases
19	nsv894148	chr9:136874066-137093168	Enhancers Strong transcription Weak transcription Bivalent/Poised TSS ZNF genes & repeats Active TSS Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
20	nsv894149	chr9:136874158-136950691	Enhancers Flanking Active TSS Strong transcription Active TSS Genic enhancers Weak 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 target site	17 gene(s)	inside rSNPs	diseases
21	nsv894150	chr9:136887757-136944827	ZNF genes & repeats Flanking Active TSS Active TSS Weak transcription Strong transcription Genic enhancers Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	17 gene(s)	inside rSNPs	diseases
22	nsv894151	chr9:136887757-137397609	Weak transcription Active TSS Flanking Active TSS Strong transcription Enhancers ZNF genes & repeats Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	57 gene(s)	inside rSNPs	diseases
23	nsv466629	chr9:136893867-136938961	Genic enhancers Weak transcription Strong transcription Active TSS Flanking Active TSS Enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	12 gene(s)	inside rSNPs	diseases
24	nsv615779	chr9:136893867-136938961	Active TSS Weak transcription Strong transcription Flanking Active TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	12 gene(s)	inside rSNPs	diseases
25	esv1806029	chr9:136906752-136933825	Weak transcription Strong transcription Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Genic enhancers Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
26	nsv430110	chr9:136909280-136964450	Weak transcription Genic enhancers Flanking Active TSS Strong transcription Enhancers Bivalent Enhancer Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases

mRNA abundance (count:5)

SNP	Gene	Cis/trans	Tissue	Source
rs2073818	QRFP	cis	cerebellum	SCAN
rs2073818	BRD3	cis	parietal	SCAN
rs2073818	BRD3	cis	lymphoblastoid	seeQTL
rs2073818	CARD9	cis	parietal	SCAN
rs2073818	GTF3C4	cis	parietal	SCAN

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:136891800-136919400	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
2	chr9:136892000-136919400	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
3	chr9:136892000-136919600	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
4	chr9:136892000-136920200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr9:136892000-136921200	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr9:136892000-136922800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
7	chr9:136892400-136920400	Strong transcription	Primary hematopoietic stem cells short term culture	blood
8	chr9:136892600-136919400	Strong transcription	Fetal Thymus	thymus
9	chr9:136893800-136920000	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
10	chr9:136894400-136918800	Strong transcription	HUES48 Cell Line	embryonic stem cell
11	chr9:136894400-136919200	Strong transcription	Primary neutrophils fromperipheralblood	blood
12	chr9:136894400-136920200	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
13	chr9:136895000-136919000	Strong transcription	iPS-20b Cell Line	embryonic stem cell
14	chr9:136895400-136919000	Strong transcription	Primary T helper cells fromperipheralblood	blood
15	chr9:136895800-136920000	Strong transcription	HUES6 Cell Line	embryonic stem cell
16	chr9:136895800-136920000	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
17	chr9:136896200-136920600	Strong transcription	Dnd41	blood
18	chr9:136899200-136924600	Weak transcription	GM12878-XiMat	blood
19	chr9:136901600-136923600	Weak transcription	HUVEC	blood vessel
20	chr9:136903000-136919400	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
21	chr9:136903000-136919600	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
22	chr9:136903200-136918800	Strong transcription	H1 Cell Line	embryonic stem cell
23	chr9:136903200-136918800	Strong transcription	Ovary	ovary
24	chr9:136903200-136919200	Strong transcription	Primary T cells from cord blood	blood
25	chr9:136903600-136918800	Strong transcription	H9 Cell Line	embryonic stem cell
26	chr9:136903600-136919000	Strong transcription	Lung	lung
27	chr9:136903600-136919600	Strong transcription	Primary monocytes fromperipheralblood	blood
28	chr9:136903600-136920000	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
29	chr9:136903600-136927000	Strong transcription	Thymus	Thymus
30	chr9:136903800-136919400	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
31	chr9:136904200-136919000	Strong transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
32	chr9:136904200-136919800	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
33	chr9:136904400-136919800	Strong transcription	iPS-15b Cell Line	embryonic stem cell
34	chr9:136904600-136920800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
35	chr9:136904800-136920600	Strong transcription	Fetal Brain Female	brain
36	chr9:136904800-136920800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
37	chr9:136905200-136919200	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
38	chr9:136905200-136919800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
39	chr9:136905200-136919800	Strong transcription	Cortex derived primary cultured neurospheres	brain
40	chr9:136905200-136920400	Weak transcription	Small Intestine	intestine
41	chr9:136906600-136918800	Strong transcription	Duodenum Smooth Muscle	Duodenum
42	chr9:136906600-136920600	Strong transcription	Fetal Stomach	stomach
43	chr9:136906800-136919000	Strong transcription	Placenta Amnion	Placenta Amnion
44	chr9:136906800-136920400	Strong transcription	Brain Germinal Matrix	brain
45	chr9:136907000-136920000	Strong transcription	Monocytes-CD14+_RO01746	blood
46	chr9:136907200-136920000	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
47	chr9:136907600-136920400	Weak transcription	Fetal Heart	heart
48	chr9:136908600-136919000	Strong transcription	Primary T helper cells PMA-I stimulated	--
49	chr9:136908600-136919000	Strong transcription	Colonic Mucosa	Colon
50	chr9:136908600-136919200	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links