Variant report

Variant	rs10739098
Chromosome Location	chr9:6417677-6417678
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:15)
CpG islands
(count:0)
Chromatin interactive
region (count:6)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:15 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	SPI1	chr9:6417079-6417748	HL-60	blood:	n/a	chr9:6417215-6417224
2	SPI1	chr9:6417013-6417771	GM12878	blood:	n/a	chr9:6417215-6417224
3	CUX1	chr9:6417366-6417683	GM12878	blood:	n/a	n/a
4	TBP	chr9:6417260-6417856	GM12878	blood:	n/a	n/a
5	EP300	chr9:6417330-6417909	GM12878	blood:	n/a	n/a
6	MAX	chr9:6417204-6417798	NB4	blood:	n/a	n/a
7	MXI1	chr9:6417303-6417887	GM12878	blood:	n/a	n/a
8	CEBPB	chr9:6417110-6417921	IMR90	lung:	n/a	n/a
9	EP300	chr9:6417329-6418130	GM12878	blood:	n/a	n/a
10	POLR2A	chr9:6417582-6417879	GM12878	blood:	n/a	n/a
11	NFIC	chr9:6417142-6418147	GM12878	blood:	n/a	n/a
12	TBL1XR1	chr9:6417284-6417890	GM12878	blood:	n/a	n/a
13	STAT3	chr9:6417587-6417917	GM12878	blood:	n/a	n/a
14	CHD1	chr9:6417108-6417866	GM12878	blood:	n/a	n/a
15	IKZF1	chr9:6417629-6418318	GM12878	blood:	n/a	n/a

No data

(count:6 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr9:6412902..6414944-chr9:6415944..6418989,4	MCF-7	breast:
2	chr9:6417024..6418829-chr9:6426585..6429333,3	K562	blood:
3	chr9:6417292..6420636-chr9:6422611..6425827,4	K562	blood:
4	chr9:6417367..6418926-chr9:6465280..6467264,2	MCF-7	breast:
5	chr9:6413244..6414955-chr9:6415894..6417896,3	MCF-7	breast:
6	chr9:6412634..6415362-chr9:6415861..6419998,11	K562	blood:

No data

Variant related genes	Relation type
UHRF2	TF binding region
ENSG00000147854	Chromatin interaction

Extended variants
information (count: 111 )
Associated
traits (count: 3 )

rSNPs within LD-proxies of this variant (count:100)

rs_ID	r²[population]
rs10115362	0.88[ASN][1000 genomes]
rs10115883	0.94[CHD][hapmap];0.82[GIH][hapmap];0.89[JPT][hapmap]
rs10122116	0.94[JPT][hapmap]
rs10124572	0.87[ASN][1000 genomes]
rs10733529	0.81[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10739099	0.94[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.81[YRI][hapmap];0.85[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10739100	0.95[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10739102	0.93[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs10758783	0.87[ASN][1000 genomes]
rs10758784	0.89[ASW][hapmap];0.94[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.97[GIH][hapmap];0.94[JPT][hapmap];0.90[MKK][hapmap];0.90[TSI][hapmap];0.89[YRI][hapmap];0.82[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs10758785	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];0.94[JPT][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10758786	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10758787	0.98[AFR][1000 genomes];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10758788	0.94[CEU][hapmap];1.00[CHB][hapmap];0.94[JPT][hapmap];0.80[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs10758789	0.94[CEU][hapmap];1.00[CHB][hapmap];0.94[CHD][hapmap];1.00[GIH][hapmap];0.94[JPT][hapmap];0.93[MEX][hapmap];1.00[TSI][hapmap];0.87[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10758790	0.89[ASW][hapmap];0.94[CEU][hapmap];1.00[CHB][hapmap];0.94[CHD][hapmap];1.00[GIH][hapmap];0.94[JPT][hapmap];0.81[LWK][hapmap];0.85[MEX][hapmap];0.84[MKK][hapmap];0.96[TSI][hapmap];0.85[YRI][hapmap];0.85[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10758791	0.92[AMR][1000 genomes];0.92[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs10758792	0.92[AMR][1000 genomes];0.96[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs10815428	0.94[CHB][hapmap];1.00[JPT][hapmap];0.87[ASN][1000 genomes]
rs10815432	0.81[ASN][1000 genomes]
rs10815435	0.90[AMR][1000 genomes];0.96[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs10975579	0.89[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs10975582	0.90[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs10975583	0.89[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.90[MKK][hapmap];1.00[TSI][hapmap];0.89[YRI][hapmap];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs10975585	0.93[ASN][1000 genomes]
rs10975595	0.82[CEU][hapmap];0.88[CHD][hapmap];0.91[GIH][hapmap];1.00[JPT][hapmap];0.83[TSI][hapmap];0.87[ASN][1000 genomes]
rs10975605	0.94[CHD][hapmap];0.82[GIH][hapmap];0.89[JPT][hapmap]
rs1156747	1.00[CHB][hapmap];0.88[CHD][hapmap];0.85[GIH][hapmap];0.94[JPT][hapmap];0.81[LWK][hapmap];0.87[MKK][hapmap];0.85[YRI][hapmap];0.94[ASN][1000 genomes]
rs11790625	0.89[ASN][1000 genomes]
rs11791651	0.88[JPT][hapmap];0.84[ASN][1000 genomes]
rs11795355	0.89[JPT][hapmap]
rs12346455	0.89[CEU][hapmap];0.82[CHB][hapmap];0.86[CHD][hapmap];0.82[GIH][hapmap];0.89[JPT][hapmap];0.82[MKK][hapmap];0.84[TSI][hapmap];0.85[ASN][1000 genomes]
rs12347573	0.82[CEU][hapmap];0.88[JPT][hapmap]
rs12351293	0.87[ASN][1000 genomes]
rs12376117	0.87[ASN][1000 genomes]
rs1322171	0.80[ASN][1000 genomes]
rs13283381	0.82[CEU][hapmap];0.82[CHB][hapmap];0.94[CHD][hapmap];0.84[JPT][hapmap];0.84[TSI][hapmap]
rs13291472	0.87[CEU][hapmap];0.82[CHB][hapmap];0.89[JPT][hapmap]
rs13292799	0.89[ASN][1000 genomes]
rs13298500	0.80[CHB][hapmap];0.94[CHD][hapmap];0.82[JPT][hapmap]
rs13440427	0.83[ASN][1000 genomes]
rs1381035	0.91[CEU][hapmap];1.00[CHB][hapmap];0.94[JPT][hapmap];0.80[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1381036	0.87[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1381037	0.84[AMR][1000 genomes];0.95[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1575263	0.80[ASN][1000 genomes]
rs1575264	0.80[ASN][1000 genomes]
rs16924328	0.83[CHB][hapmap];0.95[JPT][hapmap]
rs16924562	0.94[JPT][hapmap];0.86[ASN][1000 genomes]
rs16924591	0.86[ASN][1000 genomes]
rs16924624	0.82[CHB][hapmap];0.89[JPT][hapmap]
rs16924626	0.94[JPT][hapmap]
rs16924631	0.82[CHB][hapmap];0.83[CHD][hapmap];0.94[JPT][hapmap]
rs16924634	0.88[CHD][hapmap];0.84[JPT][hapmap]
rs1824537	0.99[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1870696	0.82[CHD][hapmap];0.94[JPT][hapmap];0.85[ASN][1000 genomes]
rs1903419	0.89[ASW][hapmap];0.94[CEU][hapmap];0.88[CHB][hapmap];0.88[CHD][hapmap];0.94[GIH][hapmap];1.00[JPT][hapmap];0.93[MEX][hapmap];0.87[MKK][hapmap];1.00[TSI][hapmap];0.81[YRI][hapmap];0.92[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2065074	0.87[AMR][1000 genomes];0.89[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2065075	0.81[AFR][1000 genomes];0.89[AMR][1000 genomes];0.95[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2169283	0.94[CHB][hapmap];0.88[CHD][hapmap];1.00[GIH][hapmap];0.84[JPT][hapmap];0.81[MKK][hapmap];0.86[TSI][hapmap];0.92[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs2169286	1.00[CHB][hapmap];0.84[JPT][hapmap];0.93[ASN][1000 genomes]
rs2381444	0.93[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs33962342	0.82[CHD][hapmap]
rs3739654	0.89[CEU][hapmap];0.86[CHD][hapmap];0.85[GIH][hapmap];0.89[JPT][hapmap];0.84[MKK][hapmap];0.84[TSI][hapmap];0.84[ASN][1000 genomes]
rs380674	0.92[AMR][1000 genomes];0.96[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs394137	0.88[AMR][1000 genomes];0.96[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs414107	0.80[AMR][1000 genomes];0.95[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs4380997	0.82[ASN][1000 genomes]
rs4384035	0.88[ASN][1000 genomes]
rs452135	0.96[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs4556138	0.83[ASN][1000 genomes]
rs4740844	0.94[CEU][hapmap];1.00[CHB][hapmap];0.94[JPT][hapmap];0.80[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4740845	0.80[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4742199	0.97[ASN][1000 genomes]
rs4742201	0.94[CEU][hapmap];1.00[CHB][hapmap];0.94[CHD][hapmap];1.00[GIH][hapmap];0.94[JPT][hapmap];0.85[MEX][hapmap];0.87[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4742202	0.94[CEU][hapmap];1.00[CHB][hapmap];0.94[CHD][hapmap];1.00[GIH][hapmap];0.94[JPT][hapmap];0.93[MEX][hapmap];1.00[TSI][hapmap];0.87[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4742204	0.87[AMR][1000 genomes];0.92[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs504698	0.86[ASN][1000 genomes]
rs530722	0.84[ASN][1000 genomes]
rs55960819	0.87[ASN][1000 genomes]
rs56218473	0.92[ASN][1000 genomes]
rs56396114	0.87[ASN][1000 genomes]
rs56939673	0.90[ASN][1000 genomes]
rs569866	0.86[ASN][1000 genomes]
rs6477086	0.82[ASN][1000 genomes]
rs6477087	0.82[CEU][hapmap];0.94[CHD][hapmap];0.85[GIH][hapmap];0.89[JPT][hapmap];0.82[MKK][hapmap];0.87[TSI][hapmap]
rs67852216	0.88[ASN][1000 genomes]
rs7027302	0.87[ASN][1000 genomes]
rs7029772	0.82[CHB][hapmap];0.83[JPT][hapmap]
rs7033940	0.86[ASN][1000 genomes]
rs73401679	0.86[ASN][1000 genomes]
rs7852539	0.94[CEU][hapmap];0.89[JPT][hapmap]
rs7853059	0.86[ASN][1000 genomes]
rs7853834	0.86[ASN][1000 genomes]
rs7857628	1.00[CHB][hapmap];0.88[CHD][hapmap];0.94[JPT][hapmap];0.86[ASN][1000 genomes]
rs7860427	0.88[ASN][1000 genomes]
rs7860966	0.91[ASN][1000 genomes]
rs7861073	0.91[ASN][1000 genomes]
rs7861559	0.91[ASN][1000 genomes]
rs7865955	1.00[CHB][hapmap];0.88[CHD][hapmap];0.94[JPT][hapmap];0.87[ASN][1000 genomes]
rs7871134	0.92[AMR][1000 genomes];0.96[EUR][1000 genomes];0.88[ASN][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	nsv948847	chr9:5712626-6417677	Strong transcription Enhancers Weak transcription Flanking Active TSS Active TSS 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 miRNA target site	39 gene(s)	inside rSNPs	diseases
2	nsv1031086	chr9:5806949-6630686	Strong transcription Enhancers Weak transcription Active TSS Flanking Active TSS Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	42 gene(s)	inside rSNPs	diseases
3	nsv539967	chr9:5806949-6630686	Flanking Active TSS Enhancers Strong transcription Weak transcription Genic enhancers Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	42 gene(s)	inside rSNPs	diseases
4	nsv933124	chr9:6099101-6644738	Weak transcription Genic enhancers Bivalent Enhancer Flanking Active TSS Strong transcription Enhancers Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	28 gene(s)	inside rSNPs	diseases
5	nsv1029000	chr9:6188652-6687205	Enhancers Strong transcription Weak transcription Active TSS Transcr. at gene 5' and 3' Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	68 gene(s)	inside rSNPs	diseases
6	nsv1031459	chr9:6216913-6657192	Active TSS Weak transcription Enhancers ZNF genes & repeats Strong transcription Flanking Active TSS Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	29 gene(s)	inside rSNPs	diseases
7	nsv948562	chr9:6222553-6684955	Bivalent/Poised TSS Flanking Active TSS Weak transcription Strong transcription Genic enhancers Enhancers Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	67 gene(s)	inside rSNPs	diseases
8	nsv1032350	chr9:6328167-6630686	Strong transcription Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	22 gene(s)	inside rSNPs	diseases
9	nsv892160	chr9:6364449-6506038	Weak transcription Genic enhancers Strong transcription Enhancers Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	19 gene(s)	inside rSNPs	diseases
10	nsv892161	chr9:6364449-6523056	Enhancers Bivalent/Poised TSS Strong transcription Weak transcription Genic enhancers Flanking Active TSS ZNF genes & repeats Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	19 gene(s)	inside rSNPs	diseases
11	nsv831497	chr9:6377501-6612402	Weak transcription Flanking Active TSS Genic enhancers Enhancers Strong transcription Active TSS 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	21 gene(s)	inside rSNPs	diseases

mRNA abundance (count:3)

SNP	Gene	Cis/trans	Tissue	Source
rs10739098	PDCD1LG2	cis	parietal	SCAN
rs10739098	C9orf38	Cis_1M	lymphoblastoid	RTeQTL
rs10739098	IL33	cis	parietal	SCAN

Chromatin state (count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:6414400-6427400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr9:6414600-6439400	Weak transcription	Colonic Mucosa	Colon
3	chr9:6414600-6449000	Weak transcription	Gastric	stomach
4	chr9:6414600-6449200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
5	chr9:6414600-6451800	Weak transcription	Esophagus	oesophagus
6	chr9:6414600-6477800	Weak transcription	Placenta	Placenta
7	chr9:6414800-6422000	Weak transcription	Fetal Muscle Trunk	muscle
8	chr9:6415400-6418800	Weak transcription	H9 Cell Line	embryonic stem cell
9	chr9:6415400-6418800	Weak transcription	Rectal Mucosa Donor 31	rectum
10	chr9:6415400-6419400	Enhancers	Primary T killer memory cells from peripheral blood	blood
11	chr9:6415400-6419600	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
12	chr9:6415400-6419600	Enhancers	Primary T killer naive cells fromperipheralblood	blood
13	chr9:6415400-6425400	Weak transcription	Psoas Muscle	Psoas
14	chr9:6415400-6434000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
15	chr9:6415600-6417800	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
16	chr9:6415600-6418000	Weak transcription	HUES64 Cell Line	embryonic stem cell
17	chr9:6415600-6418600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
18	chr9:6415600-6418600	Weak transcription	Adipose Nuclei	Adipose
19	chr9:6415600-6419200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
20	chr9:6415600-6419400	Enhancers	Breast Myoepithelial Primary Cells	Breast
21	chr9:6415600-6419400	Enhancers	Primary B cells from cord blood	blood
22	chr9:6415600-6420800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
23	chr9:6415600-6421000	Weak transcription	Fetal Intestine Large	intestine
24	chr9:6415600-6422000	Weak transcription	Fetal Kidney	kidney
25	chr9:6415600-6422200	Weak transcription	Lung	lung
26	chr9:6415600-6423200	Weak transcription	Stomach Mucosa	stomach
27	chr9:6415600-6430000	Weak transcription	Rectal Mucosa Donor 29	rectum
28	chr9:6415600-6431000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
29	chr9:6415600-6441200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
30	chr9:6415600-6471400	Weak transcription	Aorta	Aorta
31	chr9:6415800-6419400	Enhancers	Primary T helper naive cells fromperipheralblood	blood
32	chr9:6415800-6442800	Weak transcription	Stomach Smooth Muscle	stomach
33	chr9:6416000-6418000	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
34	chr9:6416000-6420000	Weak transcription	Fetal Intestine Small	intestine
35	chr9:6416000-6438400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
36	chr9:6416200-6418800	Weak transcription	Right Atrium	heart
37	chr9:6416200-6418800	Active TSS	GM12878-XiMat	blood
38	chr9:6416200-6419200	Enhancers	Brain Cingulate Gyrus	brain
39	chr9:6416200-6419800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
40	chr9:6416400-6417800	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
41	chr9:6416400-6417800	Genic enhancers	Hela-S3	cervix
42	chr9:6416400-6418600	Enhancers	Primary hematopoietic stem cells short term culture	blood
43	chr9:6416400-6419000	Enhancers	Fetal Brain Male	brain
44	chr9:6416400-6420600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
45	chr9:6416400-6421400	Weak transcription	Left Ventricle	heart
46	chr9:6416400-6421400	Weak transcription	Pancreas	Pancrea
47	chr9:6416400-6429800	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
48	chr9:6416400-6430000	Weak transcription	Spleen	Spleen
49	chr9:6416400-6430600	Weak transcription	Right Ventricle	heart
50	chr9:6416400-6449200	Weak transcription	H1 Cell Line	embryonic stem cell

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links