Variant report

Variant	nsv818208
Chromosome Location	chr4:3434336-3444503
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:371)
CpG islands
(count:1038)
Chromatin interactive
region (count:29)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:371 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:3443453-3443675	HepG2	liver:	n/a	n/a
2	BHLHE40	chr4:3434585-3434667	K562	blood:	n/a	n/a
3	CEBPB	chr4:3438739-3439132	Hela-S3	cervix:	n/a	n/a
4	CEBPD	chr4:3443344-3444000	HepG2	liver:	n/a	n/a
5	CHD2	chr4:3438705-3439109	Hela-S3	cervix:	n/a	n/a
6	CHD2	chr4:3444229-3444230	HepG2	liver:	n/a	n/a
7	CHD2	chr4:3442759-3442777	HepG2	liver:	n/a	n/a
8	CHD2	chr4:3443379-3443859	HepG2	liver:	n/a	chr4:3443687-3443697
9	CHD2	chr4:3438403-3438499	Hela-S3	cervix:	n/a	n/a
10	CTCF	chr4:3442660-3442810	HEEpiC	esophagus:	n/a	n/a
11	CTCF	chr4:3436560-3436710	HepG2	liver:	n/a	n/a
12	CTCF	chr4:3436640-3436790	AoAF	blood vessel:	n/a	n/a
13	CTCF	chr4:3436626-3436806	GM12878	blood:	n/a	n/a
14	CTCF	chr4:3436617-3436823	GM19239	blood:	n/a	n/a
15	CTCF	chr4:3436652-3436757	HepG2	liver:	n/a	n/a
16	CTCF	chr4:3436600-3436750	BE2_C	brain:	n/a	n/a
17	CTCF	chr4:3436640-3436790	GM12873	blood:	n/a	n/a
18	CTCF	chr4:3436570-3436853	K562	blood:	n/a	n/a
19	CTCF	chr4:3436640-3436790	SAEC	small airway:	n/a	n/a
20	CTCF	chr4:3436600-3436750	GM12867	blood:	n/a	n/a
21	CTCF	chr4:3436640-3436790	HAc	cerebellar:	n/a	n/a
22	CTCF	chr4:3436740-3436890	HPAF	blood vessel:	n/a	n/a
23	CTCF	chr4:3436600-3436750	A549	lung:	n/a	n/a
24	CTCF	chr4:3436616-3436840	H1-hESC	embryonic stem cell:	n/a	n/a
25	CTCF	chr4:3436640-3436790	MCF-7	breast:	n/a	n/a
26	CTCF	chr4:3436640-3436790	GM12864	blood:	n/a	n/a
27	CTCF	chr4:3436563-3436982	K562	blood:	n/a	n/a
28	CTCF	chr4:3436600-3436750	HFF	foreskin:	n/a	n/a
29	CTCF	chr4:3436600-3436750	SAEC	small airway:	n/a	n/a
30	CTCF	chr4:3436700-3436850	GM12869	blood:	n/a	n/a
31	CTCF	chr4:3436620-3436770	K562	blood:	n/a	n/a
32	CTCF	chr4:3436640-3436790	GM12875	blood:	n/a	n/a
33	CTCF	chr4:3436700-3436850	GM06990	blood:	n/a	n/a
34	CTCF	chr4:3436640-3436790	HRE	kidney:	n/a	n/a
35	CTCF	chr4:3436482-3436894	H1-hESC	embryonic stem cell:	n/a	n/a
36	CTCF	chr4:3436700-3436850	HCFaa	heart:	n/a	n/a
37	CTCF	chr4:3436632-3436766	IMR90	lung:	n/a	n/a
38	CTCF	chr4:3436651-3436759	GM19238	blood:	n/a	n/a
39	CTCF	chr4:3436620-3436770	HBMEC	blood vessel:	n/a	n/a
40	CTCF	chr4:3436660-3436810	GM12872	blood:	n/a	n/a
41	CTCF	chr4:3436655-3436762	GM13977	blood:	n/a	n/a
42	CTCF	chr4:3436640-3436790	GM12878	blood:	n/a	n/a
43	CTCF	chr4:3436680-3436830	HEEpiC	esophagus:	n/a	n/a
44	CTCF	chr4:3436800-3436950	BE2_C	brain:	n/a	n/a
45	CTCF	chr4:3436680-3436830	GM12866	blood:	n/a	n/a
46	CTCF	chr4:3442727-3442795	NHEK	skin:	n/a	n/a
47	CTCF	chr4:3436620-3436770	HFF-Myc	foreskin:	n/a	n/a
48	CTCF	chr4:3436600-3436750	NB4	blood:	n/a	n/a
49	CTCF	chr4:3436640-3436790	WI-38	lung:	n/a	n/a
50	CTCF	chr4:3436600-3436750	AG04449	skin:	n/a	n/a

(count:1038 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:3443735-3443785	HepG2	liver:	n/a
2	chr4:3443735-3443785	HepG2	liver:	n/a
3	chr4:3436168-3436218	Jurkat	blood:	n/a
4	chr4:3443694-3443744	HUVEC	blood vessel:	n/a
5	chr4:3443656-3443706	AG10803	skin:	n/a
6	chr4:3443656-3443706	HCM	heart:	n/a
7	chr4:3443608-3443658	LNCaP	prostate:	n/a
8	chr4:3443025-3443075	RPTEC	kidney:	n/a
9	chr4:3442962-3443012	AG04449	skin:	fetal
10	chr4:3442311-3442361	K562	blood:	n/a
11	chr4:3442311-3442361	NH-A	brain:	n/a
12	chr4:3444147-3444197	NHDF-neo	bronchial:	n/a
13	chr4:3444147-3444197	HepG2	liver:	n/a
14	chr4:3442962-3443012	ECC-1	luminal epithelium:	n/a
15	chr4:3443735-3443785	AG04450	lung:	fetal
16	chr4:3443694-3443744	Hela-S3	cervix:	n/a
17	chr4:3444147-3444197	ECC-1	luminal epithelium:	n/a
18	chr4:3443625-3443675	SK-N-MC	brain:	n/a
19	chr4:3443683-3443733	HEK293	kidney:	embryo
20	chr4:3444147-3444197	HAEpiC	amniotic membrane:	n/a
21	chr4:3435449-3435499	HEK293	kidney:	embryo
22	chr4:3435449-3435499	HMEC	breast:	n/a
23	chr4:3442311-3442361	GM06990	blood:	n/a
24	chr4:3443625-3443675	HepG2	liver:	n/a
25	chr4:3435449-3435499	AoSMC	blood vessel:	n/a
26	chr4:3443683-3443733	NHBE	bronchial:	n/a
27	chr4:3438579-3438629	NH-A	brain:	n/a
28	chr4:3444147-3444197	AG04450	lung:	fetal
29	chr4:3436404-3436454	HUVEC	blood vessel:	n/a
30	chr4:3435525-3435575	K562	blood:	n/a
31	chr4:3435449-3435499	HPAEpiC	pulmonary alveolar:	n/a
32	chr4:3444147-3444197	HRE	kidney:	n/a
33	chr4:3436404-3436454	T-47D	breast:	n/a
34	chr4:3435449-3435499	HUVEC	blood vessel:	n/a
35	chr4:3435498-3435548	H1-hESC	embryonic stem cell:	embryo
36	chr4:3443656-3443706	ECC-1	luminal epithelium:	n/a
37	chr4:3443694-3443744	AG09319	gingival:	n/a
38	chr4:3439095-3439145	HUVEC	blood vessel:	n/a
39	chr4:3443625-3443675	SK-N-SH	brain:	n/a
40	chr4:3436404-3436454	NHBE	bronchial:	n/a
41	chr4:3443735-3443785	Caco-2	colon:	n/a
42	chr4:3443656-3443706	HNPCEpiC	eye:	n/a
43	chr4:3443683-3443733	ECC-1	luminal epithelium:	n/a
44	chr4:3438579-3438629	IMR90	lung:	fetal
45	chr4:3435525-3435575	H1-hESC	embryonic stem cell:	embryo
46	chr4:3435498-3435548	PANC-1	pancreas:	n/a
47	chr4:3442962-3443012	HCM	heart:	n/a
48	chr4:3443735-3443785	HCT-116	colon:	n/a
49	chr4:3443025-3443075	AG10803	skin:	n/a
50	chr4:3439095-3439145	Hepatocyte	liver:	n/a

(count:29 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:3439130..3442230-chr4:3483136..3486025,3	MCF-7	breast:
2	chr4:3438642..3440686-chr4:3450024..3452220,2	MCF-7	breast:
3	chr4:3433662..3435560-chr4:3437260..3439057,2	MCF-7	breast:
4	chr4:3438822..3441284-chr4:3443467..3446994,3	K562	blood:
5	chr4:3293054..3295146-chr4:3436472..3438232,3	MCF-7	breast:
6	chr4:3347550..3348452-chr4:3441019..3441869,2	K562	blood:
7	chr4:3437523..3439091-chr4:3448156..3450987,2	MCF-7	breast:
8	chr4:3417191..3419894-chr4:3434904..3438347,3	MCF-7	breast:
9	chr4:3340754..3343218-chr4:3436055..3438880,2	MCF-7	breast:
10	chr4:3355212..3358066-chr4:3437874..3440532,4	MCF-7	breast:
11	chr4:3351060..3353090-chr4:3436592..3439411,2	MCF-7	breast:
12	chr12:52607035..52609334-chr4:3440706..3442862,2	MCF-7	breast:
13	chr4:3438758..3441335-chr4:3441966..3444505,4	MCF-7	breast:
14	chr4:3437849..3440325-chr4:3440402..3441941,2	MCF-7	breast:
15	chr4:3387900..3390200-chr4:3439176..3442077,2	MCF-7	breast:
16	chr4:3428890..3430804-chr4:3441748..3443973,2	MCF-7	breast:
17	chr4:3293753..3295526-chr4:3439987..3441578,2	MCF-7	breast:
18	chr4:3433662..3435560-chr4:3437260..3439057,2	MCF-7	breast:
19	chr4:3437849..3440325-chr4:3440402..3441941,2	MCF-7	breast:
20	chr4:3416652..3419915-chr4:3441173..3444245,3	MCF-7	breast:
21	chr4:3428384..3430154-chr4:3434283..3437033,2	K562	blood:
22	chr4:3430343..3432771-chr4:3437903..3441095,3	K562	blood:
23	chr4:3297878..3299647-chr4:3439847..3442316,2	MCF-7	breast:
24	chr4:3439707..3441284-chr4:3443467..3445284,2	K562	blood:
25	chr4:3438186..3441523-chr4:3461903..3464658,4	MCF-7	breast:
26	chr4:3438145..3440558-chr4:3486054..3488354,2	MCF-7	breast:
27	chr4:3432116..3434989-chr4:3463177..3465142,2	MCF-7	breast:
28	chr4:3432863..3436671-chr4:3438111..3441622,5	K562	blood:
29	chr4:3432863..3436671-chr4:3438111..3441622,5	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RGS12-1	chr4:3441182-3441640	NONHSAT094871

No data

Variant related genes	Relation type
HGFAC	TF binding region
HGFAC	CpG island
ENSG00000109758	chromatin interactions
ENSG00000175920	chromatin interactions
ENSG00000159788	chromatin interactions

Extended variants
information (count: 525 )
Associated
traits (count: 60 )

Variant overlapped rSNPs/rCNVs (count:525 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4690096	chr4:3434336-3434337	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs552654480	chr4:3434337-3434338	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs34652982	chr4:3434339-3434340	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs116389749	chr4:3434351-3434352	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs150254534	chr4:3434352-3434353	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs556933464	chr4:3434356-3434357	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs574024565	chr4:3434403-3434404	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs373648297	chr4:3434494-3434495	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs553032423	chr4:3434538-3434539	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs187748908	chr4:3434548-3434549	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs193097529	chr4:3434562-3434563	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs111940909	chr4:3434572-3434573	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs185535591	chr4:3434589-3434590	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs575704704	chr4:3434595-3434596	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs559292716	chr4:3434600-3434601	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs544801196	chr4:3434617-3434618	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs149443834	chr4:3434629-3434630	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs147350327	chr4:3434630-3434631	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs112220249	chr4:3434642-3434643	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs190162463	chr4:3434654-3434655	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs375015551	chr4:3434691-3434692	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs560079066	chr4:3434772-3434773	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs532390859	chr4:3434785-3434786	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs547035494	chr4:3434811-3434812	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs569342617	chr4:3434848-3434849	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs536844670	chr4:3434850-3434851	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs111971959	chr4:3434854-3434855	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs6818397	chr4:3434885-3434886	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
29	rs143475051	chr4:3434915-3434916	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs577642050	chr4:3434922-3434923	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs147170498	chr4:3434926-3434927	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs538633469	chr4:3434928-3434929	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs16844345	chr4:3434931-3434932	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs374510502	chr4:3434932-3434933	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs575341415	chr4:3434943-3434944	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs544478321	chr4:3434956-3434957	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs554774718	chr4:3434968-3434969	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs574705279	chr4:3434999-3435000	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs76122010	chr4:3435007-3435008	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs74628447	chr4:3435029-3435030	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs532331930	chr4:3435051-3435052	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs546217962	chr4:3435063-3435064	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs562838724	chr4:3435075-3435076	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs531860799	chr4:3435076-3435077	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs374732544	chr4:3435213-3435214	Weak transcription Active TSS Genic enhancers Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs550487744	chr4:3435232-3435233	Weak transcription Active TSS Genic enhancers Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs374536054	chr4:3435260-3435261	Weak transcription Active TSS Genic enhancers Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs567434691	chr4:3435266-3435267	Weak transcription Active TSS Genic enhancers Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs59468921	chr4:3435269-3435270	Weak transcription Active TSS Genic enhancers Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs546870614	chr4:3435285-3435286	Weak transcription Active TSS Genic enhancers Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:60)

Disease	PMID	Source
Retinitis pigmentosa	18421352	CNVD
Wolf-Hirschhorn syndrome	19259404	CNVD
Bladder cancer	19242612	CNVD
Breast cancer	19242612	CNVD
Congenital anomalies of the kidney and urinary tract	19242612	CNVD
abnormal development	18461090	CNVD
Olfactory neuroblastoma	18408657	CNVD
Wilms tumour	21544195	CNVD
Melanoma	20688739	CNVD
Colorectal cancer	16272173	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17603634	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Colorectal cancer	19359472	CNVD
Neuroblastoma	17533364	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Cancer	21637783	CNVD
Melanoma	21693616	CNVD
Squamous cell cancer	21044232	CNVD
Colorectal cancer	20709793	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Non-small cell lung cancer	21044232	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	17387387	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Cervical cancer	21062161	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Glioblastoma multiforme	21080181	CNVD
Chordoma	21602918	CNVD
HIV/AIDS	22032296	CNVD
Neuroblastoma	18923191	CNVD
small cell lung cancer	20016488	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Urothelial carcinoma	21177765	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Lung cancer	18438408	CNVD
Prostate cancer	18632612	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Breast cancer	21785460	CNVD
Myelofibrosis	22110671	CNVD
Schizophrenia	21399695	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	21509527	CNVD
Ependymoma	20639864	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Breast cancer	22522925	CNVD
Schizophrenia	23813976	CNVD

Chromatin state (count:319 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:3408800-3436600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
2	chr4:3411000-3436400	Strong transcription	Fetal Intestine Small	intestine
3	chr4:3411200-3436400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
4	chr4:3411200-3436600	Weak transcription	HUES6 Cell Line	embryonic stem cell
5	chr4:3413600-3437000	Strong transcription	Esophagus	oesophagus
6	chr4:3415000-3435600	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
7	chr4:3415000-3436400	Strong transcription	Cortex derived primary cultured neurospheres	brain
8	chr4:3415400-3437000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
9	chr4:3415800-3436400	Strong transcription	Lung	lung
10	chr4:3416400-3436200	Weak transcription	HUES48 Cell Line	embryonic stem cell
11	chr4:3416400-3436800	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
12	chr4:3416600-3435600	Strong transcription	Skeletal Muscle Male	skeletal muscle
13	chr4:3416600-3437800	Weak transcription	Stomach Mucosa	stomach
14	chr4:3416800-3436600	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
15	chr4:3416800-3438400	Weak transcription	NHDF-Ad	bronchial
16	chr4:3417200-3435600	Strong transcription	Fetal Intestine Large	intestine
17	chr4:3417200-3444800	Weak transcription	Primary hematopoietic stem cells	blood
18	chr4:3417800-3435200	Strong transcription	Adipose Nuclei	Adipose
19	chr4:3417800-3435200	Strong transcription	Fetal Brain Female	brain
20	chr4:3418200-3436600	Strong transcription	Breast Myoepithelial Primary Cells	Breast
21	chr4:3418200-3438000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
22	chr4:3418200-3438000	Weak transcription	A549	lung
23	chr4:3419000-3434600	Weak transcription	Primary T helper cells fromperipheralblood	blood
24	chr4:3419200-3444600	Weak transcription	Primary monocytes fromperipheralblood	blood
25	chr4:3419400-3438400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
26	chr4:3419600-3435600	Weak transcription	Primary T helper cells PMA-I stimulated	--
27	chr4:3419600-3438400	Weak transcription	NH-A	brain
28	chr4:3419800-3435200	Weak transcription	Rectal Mucosa Donor 29	rectum
29	chr4:3419800-3438800	Weak transcription	NHLF	lung
30	chr4:3420000-3437000	Strong transcription	Brain Germinal Matrix	brain
31	chr4:3420200-3438400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
32	chr4:3420400-3435200	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
33	chr4:3420400-3436000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
34	chr4:3420400-3436600	Weak transcription	Fetal Brain Male	brain
35	chr4:3420400-3438200	Weak transcription	Muscle Satellite Cultured Cells	--
36	chr4:3420400-3438600	Weak transcription	Monocytes-CD14+_RO01746	blood
37	chr4:3420600-3435600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
38	chr4:3420600-3436400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
39	chr4:3422200-3435200	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
40	chr4:3423600-3437400	Strong transcription	Fetal Stomach	stomach
41	chr4:3424400-3435400	Strong transcription	Foreskin Melanocyte Primary Cells skin01	Skin
42	chr4:3425600-3438400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
43	chr4:3425800-3438600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
44	chr4:3426000-3436400	Weak transcription	H1 Cell Line	embryonic stem cell
45	chr4:3427000-3437800	Weak transcription	HMEC	breast
46	chr4:3427000-3442000	Weak transcription	Colon Smooth Muscle	Colon
47	chr4:3427000-3443200	Weak transcription	Brain Substantia Nigra	brain
48	chr4:3427200-3437800	Weak transcription	Brain Angular Gyrus	brain
49	chr4:3427200-3438400	Weak transcription	HUVEC	blood vessel
50	chr4:3427600-3436200	Strong transcription	Fetal Muscle Leg	muscle

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