Variant report

Variant	nsv1010207
Chromosome Location	chr4:99291295-99312807
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:99308616-99309381	K562	blood:	n/a	n/a
2	BHLHE40	chr4:99308859-99308960	K562	blood:	n/a	n/a
3	BRCA1	chr4:99306628-99306634	GM12878	blood:	n/a	n/a
4	CCNT2	chr4:99295425-99295560	K562	blood:	n/a	n/a
5	CEBPB	chr4:99308849-99309204	K562	blood:	n/a	n/a
6	CEBPB	chr4:99302540-99302810	IMR90	lung:	n/a	n/a
7	CTCF	chr4:99309289-99309306	GM10266	blood:	n/a	n/a
8	CTCF	chr4:99309293-99309332	Hela-S3	cervix:	n/a	chr4:99309296-99309317 chr4:99309302-99309318 chr4:99309301-99309319
9	CTCF	chr4:99309212-99309462	GM12878	blood:	n/a	chr4:99309296-99309317 chr4:99309302-99309318 chr4:99309301-99309319
10	CTCF	chr4:99309125-99309373	HepG2	liver:	n/a	chr4:99309296-99309317 chr4:99309302-99309318 chr4:99309301-99309319
11	CTCF	chr4:99309305-99309310	Medullo	brain:	n/a	n/a
12	CTCF	chr4:99295859-99295860	Spleen_OC	spleen:	n/a	n/a
13	CUX1	chr4:99308806-99309193	K562	blood:	n/a	n/a
14	E2F4	chr4:99298750-99299030	MCF10A-Er-Src	breast:	n/a	n/a
15	E2F4	chr4:99304606-99304806	MCF10A-Er-Src	breast:	n/a	n/a
16	E2F4	chr4:99297500-99297915	MCF10A-Er-Src	breast:	n/a	n/a
17	ELK1	chr4:99299018-99299126	GM12878	blood:	n/a	n/a
18	EP300	chr4:99308794-99309169	K562	blood:	n/a	n/a
19	EP300	chr4:99304847-99304907	GM12878	blood:	n/a	n/a
20	EP300	chr4:99312227-99312624	SK-N-SH_RA	brain:	n/a	n/a
21	EP300	chr4:99312244-99312601	SK-N-SH_RA	brain:	n/a	n/a
22	FOS	chr4:99298825-99299025	MCF10A-Er-Src	breast:	n/a	chr4:99298949-99298956 chr4:99298947-99298956
23	FOS	chr4:99298795-99299038	MCF10A-Er-Src	breast:	n/a	chr4:99298949-99298956 chr4:99298947-99298956
24	FOS	chr4:99298802-99299073	MCF10A-Er-Src	breast:	n/a	chr4:99298949-99298956 chr4:99298947-99298956
25	FOS	chr4:99298823-99299075	MCF10A-Er-Src	breast:	n/a	chr4:99298949-99298956 chr4:99298947-99298956
26	FOS	chr4:99302616-99302685	MCF10A-Er-Src	breast:	n/a	chr4:99302673-99302683 chr4:99302673-99302683 chr4:99302673-99302683
27	FOS	chr4:99302605-99302674	MCF10A-Er-Src	breast:	n/a	n/a
28	GATA1	chr4:99308546-99309583	PBDE	blood:	n/a	chr4:99308689-99308700 chr4:99309130-99309139 chr4:99309494-99309504
29	GATA3	chr4:99305543-99305743	SH-SY5Y	brain:	n/a	chr4:99305729-99305742
30	GATA3	chr4:99298299-99298927	SK-N-SH	brain:	n/a	n/a
31	GATA3	chr4:99306024-99306130	SH-SY5Y	brain:	n/a	n/a
32	IRF1	chr4:99308842-99309231	K562	blood:	n/a	n/a
33	IRF1	chr4:99308752-99309074	K562	blood:	n/a	n/a
34	IRF1	chr4:99306798-99306995	K562	blood:	n/a	chr4:99306827-99306841 chr4:99306831-99306841
35	IRF3	chr4:99300908-99300946	GM12878	blood:	n/a	n/a
36	JUN	chr4:99302555-99302743	HepG2	liver:	n/a	chr4:99302673-99302683 chr4:99302673-99302683 chr4:99302658-99302671 chr4:99302673-99302683
37	JUND	chr4:99308599-99309199	K562	blood:	n/a	n/a
38	MAFK	chr4:99311629-99311822	HepG2	liver:	n/a	chr4:99311705-99311719 chr4:99311706-99311717
39	MAFK	chr4:99308932-99308971	K562	blood:	n/a	n/a
40	MAFK	chr4:99310793-99311055	HepG2	liver:	n/a	n/a
41	MAFK	chr4:99311635-99311840	HepG2	liver:	n/a	chr4:99311705-99311719 chr4:99311706-99311717
42	MAFK	chr4:99298806-99299158	IMR90	lung:	n/a	chr4:99298958-99298969 chr4:99298957-99298971 chr4:99298845-99298854
43	MAZ	chr4:99308661-99309016	K562	blood:	n/a	n/a
44	MXI1	chr4:99311719-99311814	Hela-S3	cervix:	n/a	n/a
45	MXI1	chr4:99308948-99309012	K562	blood:	n/a	n/a
46	MYC	chr4:99308832-99309027	K562	blood:	n/a	n/a
47	NFYB	chr4:99307340-99307446	GM12878	blood:	n/a	n/a
48	POLR2A	chr4:99308074-99308077	MCF10A-Er-Src	breast:	n/a	n/a
49	POLR2A	chr4:99304873-99304881	MCF10A-Er-Src	breast:	n/a	n/a
50	POLR2A	chr4:99293978-99293994	MCF-7	breast:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:99298930-99298980	T-47D	breast:	n/a
2	chr4:99298930-99298980	HCM	heart:	n/a
3	chr4:99298930-99298980	NT2-D1	testis:	n/a
4	chr4:99298930-99298980	Jurkat	blood:	n/a
5	chr4:99298930-99298980	LNCaP	prostate:	n/a
6	chr4:99298930-99298980	K562	blood:	n/a
7	chr4:99298930-99298980	SAEC	small airway:	n/a
8	chr4:99298930-99298980	GM12891	blood:	n/a
9	chr4:99298930-99298980	PFSK-1	brain:	n/a
10	chr4:99298930-99298980	HRCEpiC	kidney:	n/a
11	chr4:99298930-99298980	NH-A	brain:	n/a
12	chr4:99298930-99298980	SK-N-SH	brain:	n/a
13	chr4:99298930-99298980	HCT-116	colon:	n/a
14	chr4:99298930-99298980	U87	brain:	n/a
15	chr4:99298930-99298980	SK-N-MC	brain:	n/a
16	chr4:99298930-99298980	Hela-S3	cervix:	n/a
17	chr4:99298930-99298980	AoSMC	blood vessel:	n/a
18	chr4:99298930-99298980	ECC-1	luminal epithelium:	n/a
19	chr4:99298930-99298980	Caco-2	colon:	n/a
20	chr4:99298930-99298980	GM19239	blood:	n/a
21	chr4:99298930-99298980	MCF10A-Er-Src	breast:	n/a
22	chr4:99298930-99298980	AG09309	skin:	n/a
23	chr4:99298930-99298980	HEK293	kidney:	embryo
24	chr4:99298930-99298980	HL-60	blood:	n/a
25	chr4:99298930-99298980	SKMC	muscle:	n/a
26	chr4:99298930-99298980	H1-hESC	embryonic stem cell:	embryo
27	chr4:99298930-99298980	IMR90	lung:	fetal
28	chr4:99298930-99298980	BJ	skin:	n/a
29	chr4:99298930-99298980	HRPEpiC	eye:	n/a
30	chr4:99298930-99298980	HRE	kidney:	n/a
31	chr4:99298930-99298980	GM12892	blood:	n/a
32	chr4:99298930-99298980	HIPEpiC	eye:	n/a
33	chr4:99298930-99298980	HUVEC	blood vessel:	n/a
34	chr4:99298930-99298980	HepG2	liver:	n/a
35	chr4:99298930-99298980	RPTEC	kidney:	n/a
36	chr4:99298930-99298980	AG04449	skin:	fetal
37	chr4:99298930-99298980	ovcar-3	ovarian:	n/a
38	chr4:99298930-99298980	GM12878	blood:	n/a
39	chr4:99298930-99298980	NB4	blood:	n/a
40	chr4:99298930-99298980	HCF	heart:	n/a
41	chr4:99298930-99298980	PANC-1	pancreas:	n/a
42	chr4:99298930-99298980	HAEpiC	amniotic membrane:	n/a
43	chr4:99298930-99298980	HCPEpiC	choroid plexus:	n/a
44	chr4:99298930-99298980	ProgFib	skin:	n/a
45	chr4:99298930-99298980	AG04450	lung:	fetal
46	chr4:99298930-99298980	CMK	blood:	n/a
47	chr4:99298930-99298980	Hepatocyte	liver:	n/a
48	chr4:99298930-99298980	PrEC	prostate:	n/a
49	chr4:99298930-99298980	AG09319	gingival:	n/a
50	chr4:99298930-99298980	GM06990	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr4:99183227..99185856-chr4:99306383..99308262,2	K562	blood:
2	chr4:99284843..99287176-chr4:99294618..99297593,2	K562	blood:
3	chr4:99063973..99066325-chr4:99305567..99308333,2	MCF-7	breast:
4	chr4:99279969..99282662-chr4:99292297..99295112,2	K562	blood:
5	chr4:99309632..99312263-chr4:99316349..99318716,2	K562	blood:
6	chr4:99298931..99300535-chr4:99303915..99306046,2	K562	blood:
7	chr4:99034025..99034574-chr4:99308766..99309435,2	MCF-7	breast:
8	chr4:99185202..99187066-chr4:99307470..99310118,2	K562	blood:
9	chr4:99300207..99302055-chr4:99309249..99311340,2	MCF-7	breast:
10	chr4:99297214..99300431-chr4:99303291..99306046,3	K562	blood:
11	chr4:99072160..99072897-chr4:99308436..99309402,2	MCF-7	breast:

Variant related genes	Relation type
RAP1GDS1	TF binding region
RAP1GDS1	CpG island
ENSG00000138698	chromatin interactions
ENSG00000163116	chromatin interactions

Extended variants
information (count: 665 )
Associated
traits (count: 76 )

Variant overlapped rSNPs/rCNVs (count:665 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs565074432	chr4:99291303-99291304	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs186697351	chr4:99291358-99291359	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs562669060	chr4:99291401-99291402	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs544531837	chr4:99291425-99291426	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs190352381	chr4:99291530-99291531	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs374762462	chr4:99291548-99291549	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs547800621	chr4:99291567-99291568	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs149714449	chr4:99291588-99291589	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs182092970	chr4:99291591-99291592	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs552349706	chr4:99291618-99291619	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs115418693	chr4:99291687-99291688	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs538141483	chr4:99291701-99291702	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs199686711	chr4:99291720-99291721	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs187649733	chr4:99291738-99291739	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs568680608	chr4:99291759-99291760	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs144646670	chr4:99291776-99291777	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs148480672	chr4:99291778-99291779	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs190931999	chr4:99291824-99291825	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs539983291	chr4:99291825-99291826	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs144124841	chr4:99291842-99291843	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs370712969	chr4:99291846-99291847	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs375084603	chr4:99291866-99291867	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs544099473	chr4:99291912-99291913	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs562769066	chr4:99291930-99291931	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs182049986	chr4:99291942-99291943	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs543565615	chr4:99291959-99291960	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs28664868	chr4:99292000-99292001	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs568278081	chr4:99292014-99292015	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs543926221	chr4:99292022-99292023	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs558831674	chr4:99292040-99292041	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs573647142	chr4:99292053-99292054	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs551886258	chr4:99292075-99292076	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs542495934	chr4:99292083-99292084	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs577148285	chr4:99292130-99292131	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs35772734	chr4:99292185-99292186	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs72688419	chr4:99292199-99292200	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs531904026	chr4:99292230-99292231	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs185159061	chr4:99292263-99292264	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs189971188	chr4:99292305-99292306	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs536157864	chr4:99292309-99292310	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs28529663	chr4:99292332-99292333	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs566117804	chr4:99292357-99292358	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs183403272	chr4:99292364-99292365	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs139798206	chr4:99292409-99292410	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs542518437	chr4:99292425-99292426	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs558258306	chr4:99292450-99292451	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs576476669	chr4:99292472-99292473	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs368079112	chr4:99292492-99292493	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs371897756	chr4:99292505-99292506	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs538007186	chr4:99292530-99292531	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:76)

Disease	PMID	Source
Acute lymphoblastic leukemia	22237106	CNVD
Glioblastoma multiforme	21080181	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Chordoma	21602918	CNVD
HIV/AIDS	22032296	CNVD
Medulloblastoma	21979893	CNVD
Neuroblastoma	18923191	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Breast cancer	21858162	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Gastric cancer	21586687	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	17603634	CNVD
Hepatocellular carcinoma	16750200	CNVD
Myxofibrosarcoma	16751306	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Breast cancer	16272173	CNVD
Colorectal cancer	19359472	CNVD
Malignant mesothelioma	18160781	CNVD
Medulloblastoma	18056178	CNVD
Multiple myeloma	17077331	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Oral squamous cell carcinoma	17134496	CNVD
4q-syndrome	17576883	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Colorectal cancer	20709793	CNVD
Muscular dystrophy	21149563	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Cervical cancer	21062161	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	16608533	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Lung cancer	19208797	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	21785460	CNVD
Myelodysplastic syndrome	21251322	CNVD
Lung cancer	18438408	CNVD
Cancer	22429812	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Autism	18414403	CNVD
Cancer	21183584	CNVD
primary effusion lymphomas	17116491	CNVD
small cell lung cancer	20016488	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17133270	CNVD
Colorectal cancer	20459617	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Hirschsprung''s Disease	21712996	CNVD
Congenital anomalies of the kidney and urinary tract	20505237	CNVD
Breast cancer	17393978	CNVD
Ovarian cancer	21720365	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Esophageal cancer	21851588	CNVD
Cancer	19907438	CNVD
Prostate cancer	16573809	CNVD
Multiple myeloma	16616336	CNVD
Melanoma	20688739	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Gastric cancer	16891809	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	16397240	CNVD

Chromatin state (count:278 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:99215000-99317000	Weak transcription	Left Ventricle	heart
2	chr4:99262800-99295600	Weak transcription	Brain Hippocampus Middle	brain
3	chr4:99262800-99333400	Weak transcription	Sigmoid Colon	Sigmoid Colon
4	chr4:99263000-99296000	Weak transcription	Brain Angular Gyrus	brain
5	chr4:99264200-99338200	Weak transcription	Skeletal Muscle Female	skeletal muscle
6	chr4:99265200-99297800	Weak transcription	Osteobl	bone
7	chr4:99265400-99298400	Weak transcription	NHDF-Ad	bronchial
8	chr4:99271600-99314800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
9	chr4:99277200-99295400	Weak transcription	Brain Anterior Caudate	brain
10	chr4:99280000-99298600	Weak transcription	NHLF	lung
11	chr4:99285000-99337800	Weak transcription	HUVEC	blood vessel
12	chr4:99285200-99294000	Weak transcription	HMEC	breast
13	chr4:99285200-99306400	Weak transcription	Pancreatic Islets	Pancreatic Islet
14	chr4:99286400-99310200	Weak transcription	Small Intestine	intestine
15	chr4:99288400-99342400	Weak transcription	A549	lung
16	chr4:99288600-99293200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
17	chr4:99288600-99295800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
18	chr4:99288600-99295800	Weak transcription	HSMMtube	muscle
19	chr4:99288600-99298600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
20	chr4:99288600-99313000	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
21	chr4:99288800-99291600	Weak transcription	Fetal Thymus	thymus
22	chr4:99288800-99293000	Weak transcription	Skeletal Muscle Male	skeletal muscle
23	chr4:99288800-99294600	Weak transcription	Primary T cells fromperipheralblood	blood
24	chr4:99288800-99295800	Weak transcription	Cortex derived primary cultured neurospheres	brain
25	chr4:99288800-99319800	Weak transcription	Fetal Muscle Trunk	muscle
26	chr4:99288800-99329200	Weak transcription	Esophagus	oesophagus
27	chr4:99288800-99332000	Weak transcription	Primary T helper cells PMA-I stimulated	--
28	chr4:99288800-99333600	Weak transcription	Rectal Mucosa Donor 29	rectum
29	chr4:99289000-99291800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
30	chr4:99289000-99291800	Weak transcription	Fetal Stomach	stomach
31	chr4:99289000-99292400	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
32	chr4:99289000-99292600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
33	chr4:99289000-99294400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
34	chr4:99289000-99295600	Weak transcription	NHEK	skin
35	chr4:99289000-99298000	Weak transcription	Muscle Satellite Cultured Cells	--
36	chr4:99289000-99298400	Strong transcription	Dnd41	blood
37	chr4:99289000-99301000	Weak transcription	Liver	Liver
38	chr4:99289000-99313600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
39	chr4:99289000-99314600	Weak transcription	Lung	lung
40	chr4:99289000-99318400	Weak transcription	Ovary	ovary
41	chr4:99289000-99333000	Weak transcription	Fetal Intestine Large	intestine
42	chr4:99289000-99333400	Weak transcription	Pancreas	Pancrea
43	chr4:99289000-99333600	Weak transcription	Rectal Mucosa Donor 31	rectum
44	chr4:99289400-99293400	Weak transcription	Aorta	Aorta
45	chr4:99289400-99316800	Weak transcription	Stomach Smooth Muscle	stomach
46	chr4:99289400-99321000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
47	chr4:99289800-99295800	Weak transcription	Fetal Muscle Leg	muscle
48	chr4:99290400-99295000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
49	chr4:99290400-99308200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
50	chr4:99290400-99308600	Weak transcription	Primary monocytes fromperipheralblood	blood

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