Variant report

Variant	esv1803957
Chromosome Location	chr4:3339038-3343475
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	CTCF	chr4:3342642-3342781	MCF-7	breast:	n/a	chr4:3342705-3342723 chr4:3342707-3342720
2	CTCF	chr4:3342577-3342854	LNCaP	prostate:	n/a	chr4:3342705-3342723 chr4:3342707-3342720
3	CTCF	chr4:3342620-3342770	GM12878	blood:	n/a	chr4:3342705-3342723 chr4:3342707-3342720
4	CTCF	chr4:3342620-3342770	HBMEC	blood vessel:	n/a	chr4:3342705-3342723 chr4:3342707-3342720
5	CTCF	chr4:3342640-3342790	WERI-Rb-1	eye:	n/a	chr4:3342705-3342723 chr4:3342707-3342720
6	CTCF	chr4:3342608-3342823	MCF-7	breast:	n/a	chr4:3342705-3342723 chr4:3342707-3342720
7	CTCF	chr4:3342640-3342790	HRE	kidney:	n/a	chr4:3342705-3342723 chr4:3342707-3342720
8	CTCF	chr4:3342566-3342873	GM12878	blood:	n/a	chr4:3342705-3342723 chr4:3342707-3342720
9	CTCF	chr4:3342640-3342790	SAEC	small airway:	n/a	chr4:3342705-3342723 chr4:3342707-3342720
10	CTCF	chr4:3342623-3342813	Pancreas_OC	pancreas:	n/a	chr4:3342705-3342723 chr4:3342707-3342720
11	CTCF	chr4:3342557-3342849	LNCaP	prostate:	n/a	chr4:3342705-3342723 chr4:3342707-3342720
12	CTCF	chr4:3342620-3342770	MCF-7	breast:	n/a	chr4:3342705-3342723 chr4:3342707-3342720
13	CTCF	chr4:3342610-3342834	NHEK	skin:	n/a	chr4:3342705-3342723 chr4:3342707-3342720
14	CTCF	chr4:3342673-3342789	GM12891	blood:	n/a	chr4:3342705-3342723 chr4:3342707-3342720
15	CTCF	chr4:3342680-3342830	AG04449	skin:	n/a	chr4:3342705-3342723 chr4:3342707-3342720
16	CTCF	chr4:3342693-3342759	GM19240	blood:	n/a	chr4:3342705-3342723 chr4:3342707-3342720
17	CTCF	chr4:3342683-3342712	GM12878	blood:	n/a	n/a
18	CTCF	chr4:3342645-3342751	Fibrobl	skin:	n/a	chr4:3342705-3342723 chr4:3342707-3342720
19	CTCF	chr4:3342614-3342803	A549	lung:	n/a	chr4:3342705-3342723 chr4:3342707-3342720
20	CTCF	chr4:3342620-3342770	HMEC	breast:	n/a	chr4:3342705-3342723 chr4:3342707-3342720
21	CTCF	chr4:3342640-3342790	AG04449	skin:	n/a	chr4:3342705-3342723 chr4:3342707-3342720
22	CTCF	chr4:3342660-3342810	GM12874	blood:	n/a	chr4:3342705-3342723 chr4:3342707-3342720
23	CTCF	chr4:3342580-3342730	NHEK	skin:	n/a	chr4:3342705-3342723 chr4:3342707-3342720
24	CTCF	chr4:3342588-3342875	MCF-7	breast:	n/a	chr4:3342705-3342723 chr4:3342707-3342720
25	CTCF	chr4:3342640-3342790	RPTEC	kidney:	n/a	chr4:3342705-3342723 chr4:3342707-3342720
26	CTCF	chr4:3342476-3342837	K562	blood:	n/a	chr4:3342705-3342723 chr4:3342707-3342720
27	CTCF	chr4:3342640-3342790	HUVEC	blood vessel:	n/a	chr4:3342705-3342723 chr4:3342707-3342720
28	CTCF	chr4:3342596-3342793	HepG2	liver:	n/a	chr4:3342705-3342723 chr4:3342707-3342720
29	CTCF	chr4:3342632-3342797	GM12892	blood:	n/a	chr4:3342705-3342723 chr4:3342707-3342720
30	CTCF	chr4:3342617-3342799	MCF-7	breast:	n/a	chr4:3342705-3342723 chr4:3342707-3342720
31	CTCF	chr4:3342660-3342810	HBMEC	blood vessel:	n/a	chr4:3342705-3342723 chr4:3342707-3342720
32	CTCF	chr4:3342542-3342802	K562	blood:	n/a	chr4:3342705-3342723 chr4:3342707-3342720
33	CTCF	chr4:3342660-3342810	MCF-7	breast:	n/a	chr4:3342705-3342723 chr4:3342707-3342720
34	CTCF	chr4:3342600-3342750	Hela-S3	cervix:	n/a	chr4:3342705-3342723 chr4:3342707-3342720
35	CTCF	chr4:3342658-3342752	HepG2	liver:	n/a	chr4:3342705-3342723 chr4:3342707-3342720
36	CTCF	chr4:3342625-3342798	H1-hESC	embryonic stem cell:	n/a	chr4:3342705-3342723 chr4:3342707-3342720
37	CTCF	chr4:3342640-3342790	GM12870	blood:	n/a	chr4:3342705-3342723 chr4:3342707-3342720
38	CTCF	chr4:3342628-3342781	Kidney_OC	kidney:	n/a	chr4:3342705-3342723 chr4:3342707-3342720
39	CTCF	chr4:3342840-3342990	HRE	kidney:	n/a	n/a
40	CTCF	chr4:3342600-3342750	HRE	kidney:	n/a	chr4:3342705-3342723 chr4:3342707-3342720
41	CTCF	chr4:3342714-3342730	Gliobla	brain:	n/a	n/a
42	CTCF	chr4:3342600-3342750	GM06990	blood:	n/a	chr4:3342705-3342723 chr4:3342707-3342720
43	CTCF	chr4:3342672-3342746	K562	blood:	n/a	chr4:3342705-3342723 chr4:3342707-3342720
44	CTCF	chr4:3342613-3342832	MCF-7	breast:	n/a	chr4:3342705-3342723 chr4:3342707-3342720
45	CTCF	chr4:3342520-3342670	HFF-Myc	foreskin:	n/a	n/a
46	CTCF	chr4:3342680-3342830	NHEK	skin:	n/a	chr4:3342705-3342723 chr4:3342707-3342720
47	CTCF	chr4:3342491-3342790	T-47D	breast:	n/a	chr4:3342705-3342723 chr4:3342707-3342720
48	CTCF	chr4:3342611-3342800	MCF-7	breast:	n/a	chr4:3342705-3342723 chr4:3342707-3342720
49	CTCF	chr4:3342580-3342730	HepG2	liver:	n/a	chr4:3342705-3342723 chr4:3342707-3342720
50	CTCF	chr4:3342605-3342747	K562	blood:	n/a	chr4:3342705-3342723 chr4:3342707-3342720

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:3342725-3342775	ovcar-3	ovarian:	n/a
2	chr4:3341177-3341227	MCF10A-Er-Src	breast:	n/a
3	chr4:3341799-3341849	T-47D	breast:	n/a
4	chr4:3341799-3341849	HNPCEpiC	eye:	n/a
5	chr4:3342111-3342161	LNCaP	prostate:	n/a
6	chr4:3341177-3341227	T-47D	breast:	n/a
7	chr4:3341799-3341849	AoSMC	blood vessel:	n/a
8	chr4:3341799-3341849	BE2_C	brain:	n/a
9	chr4:3341799-3341849	Hela-S3	cervix:	n/a
10	chr4:3342111-3342161	Jurkat	blood:	n/a
11	chr4:3341177-3341227	HEEpiC	esophagus:	n/a
12	chr4:3341937-3341987	IMR90	lung:	fetal
13	chr4:3341177-3341227	HepG2	liver:	n/a
14	chr4:3342725-3342775	NB4	blood:	n/a
15	chr4:3341799-3341849	SK-N-SH	brain:	n/a
16	chr4:3342725-3342775	Hela-S3	cervix:	n/a
17	chr4:3341177-3341227	ECC-1	luminal epithelium:	n/a
18	chr4:3341799-3341849	SKMC	muscle:	n/a
19	chr4:3342725-3342775	SK-N-SH_RA	brain:	n/a
20	chr4:3342725-3342775	Caco-2	colon:	n/a
21	chr4:3341937-3341987	GM12891	blood:	n/a
22	chr4:3342725-3342775	AG04450	lung:	fetal
23	chr4:3342725-3342775	HAEpiC	amniotic membrane:	n/a
24	chr4:3342111-3342161	PrEC	prostate:	n/a
25	chr4:3342725-3342775	HPAEpiC	pulmonary alveolar:	n/a
26	chr4:3341177-3341227	NH-A	brain:	n/a
27	chr4:3342111-3342161	NH-A	brain:	n/a
28	chr4:3341177-3341227	BJ	skin:	n/a
29	chr4:3342111-3342161	SK-N-MC	brain:	n/a
30	chr4:3341937-3341987	HCF	heart:	n/a
31	chr4:3341937-3341987	SKMC	muscle:	n/a
32	chr4:3342725-3342775	GM12878	blood:	n/a
33	chr4:3342111-3342161	SAEC	small airway:	n/a
34	chr4:3341937-3341987	HRCEpiC	kidney:	n/a
35	chr4:3342725-3342775	HepG2	liver:	n/a
36	chr4:3341799-3341849	HCF	heart:	n/a
37	chr4:3341937-3341987	PrEC	prostate:	n/a
38	chr4:3342725-3342775	NT2-D1	testis:	n/a
39	chr4:3341937-3341987	BJ	skin:	n/a
40	chr4:3341799-3341849	ovcar-3	ovarian:	n/a
41	chr4:3341177-3341227	GM06990	blood:	n/a
42	chr4:3341799-3341849	PFSK-1	brain:	n/a
43	chr4:3341799-3341849	Jurkat	blood:	n/a
44	chr4:3341799-3341849	PrEC	prostate:	n/a
45	chr4:3341177-3341227	SK-N-SH	brain:	n/a
46	chr4:3341177-3341227	AG04449	skin:	fetal
47	chr4:3342111-3342161	HCPEpiC	choroid plexus:	n/a
48	chr4:3342111-3342161	PANC-1	pancreas:	n/a
49	chr4:3341799-3341849	ProgFib	skin:	n/a
50	chr4:3342111-3342161	HIPEpiC	eye:	n/a

No.	Distal block	Cell Line	Cell type
1	chr4:3327302..3329528-chr4:3337997..3340171,2	MCF-7	breast:
2	chr4:3339088..3341066-chr4:3344153..3346803,2	MCF-7	breast:
3	chr4:3341846..3343634-chr4:3447069..3448712,2	MCF-7	breast:
4	chr4:3330743..3332280-chr4:3339908..3342252,2	MCF-7	breast:
5	chr4:3338889..3343165-chr4:3463099..3467145,4	MCF-7	breast:
6	chr4:3338818..3342772-chr4:3461368..3467187,7	MCF-7	breast:
7	chr4:3292758..3295748-chr4:3341243..3344299,3	MCF-7	breast:
8	chr4:3330077..3332907-chr4:3336771..3339582,2	K562	blood:
9	chr4:3340754..3343218-chr4:3436055..3438880,2	MCF-7	breast:
10	chr4:3339354..3341969-chr4:3342389..3344050,2	MCF-7	breast:
11	chr4:3339354..3341969-chr4:3342389..3344050,2	MCF-7	breast:
12	chr4:3321816..3324737-chr4:3338680..3341161,2	MCF-7	breast:
13	chr4:3343221..3349626-chr4:3462156..3471133,16	MCF-7	breast:
14	chr4:3292225..3296816-chr4:3337883..3341063,5	MCF-7	breast:

Variant related genes	Relation type
RGS12	TF binding region
RGS12	CpG island
ENSG00000159788	chromatin interactions
ENSG00000109758	chromatin interactions
ENSG00000175920	chromatin interactions

Extended variants
information (count: 177 )
Associated
traits (count: 56 )

Variant overlapped rSNPs/rCNVs (count:177 , 50 per page) page: 1 2 3 4

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7668784	chr4:3339038-3339039	Weak transcription ZNF genes & repeats Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs183725396	chr4:3339079-3339080	Weak transcription ZNF genes & repeats Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs116785879	chr4:3339091-3339092	Weak transcription ZNF genes & repeats Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs139820838	chr4:3339093-3339094	Weak transcription ZNF genes & repeats Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs528343242	chr4:3339120-3339121	Weak transcription ZNF genes & repeats Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs576316426	chr4:3339214-3339215	Weak transcription ZNF genes & repeats Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs551398491	chr4:3339239-3339240	Weak transcription ZNF genes & repeats Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs571231389	chr4:3339246-3339247	Weak transcription ZNF genes & repeats Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs530545631	chr4:3339268-3339269	Weak transcription ZNF genes & repeats Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs550623888	chr4:3339292-3339293	Weak transcription ZNF genes & repeats Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs567355041	chr4:3339338-3339339	Weak transcription ZNF genes & repeats Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs188161307	chr4:3339340-3339341	Weak transcription ZNF genes & repeats Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs145366416	chr4:3339341-3339342	Weak transcription ZNF genes & repeats Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs533176266	chr4:3339375-3339376	Weak transcription ZNF genes & repeats Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs370872738	chr4:3339400-3339401	Weak transcription ZNF genes & repeats Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs566959805	chr4:3339435-3339436	Weak transcription ZNF genes & repeats Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs539283982	chr4:3339437-3339438	Weak transcription ZNF genes & repeats Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs559009686	chr4:3339444-3339445	Weak transcription ZNF genes & repeats Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs114792218	chr4:3339515-3339516	Weak transcription ZNF genes & repeats Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs544182669	chr4:3339550-3339551	Weak transcription ZNF genes & repeats Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs371997489	chr4:3339584-3339585	Weak transcription ZNF genes & repeats Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs28728173	chr4:3339642-3339643	Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs140793662	chr4:3339649-3339650	Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs75326463	chr4:3339652-3339653	Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs3129335	chr4:3339664-3339665	Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs572971069	chr4:3339683-3339684	Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs149811122	chr4:3339684-3339685	Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs565155347	chr4:3339705-3339706	Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs12640526	chr4:3339728-3339729	Weak transcription Enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs182217980	chr4:3339745-3339746	Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs2749782	chr4:3339761-3339762	Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
32	rs565296055	chr4:3339809-3339810	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs529752693	chr4:3339814-3339815	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs546393236	chr4:3339894-3339895	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs377402263	chr4:3339918-3339919	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs556557035	chr4:3339931-3339932	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs116085193	chr4:3339935-3339936	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs187207208	chr4:3339981-3339982	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs190032250	chr4:3339985-3339986	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs374375726	chr4:3340007-3340008	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs368425156	chr4:3340008-3340009	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs578063331	chr4:3340033-3340034	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs538191833	chr4:3340039-3340040	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs554494647	chr4:3340062-3340063	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs369237639	chr4:3340066-3340067	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs574503130	chr4:3340067-3340068	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs13126960	chr4:3340138-3340139	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs181787761	chr4:3340222-3340223	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs185647957	chr4:3340230-3340231	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs190011814	chr4:3340231-3340232	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:56)

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
Developmental delay	21147756	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
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:153 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:3301200-3350000	Weak transcription	H9 Cell Line	embryonic stem cell
2	chr4:3314400-3348200	Weak transcription	Rectal Mucosa Donor 31	rectum
3	chr4:3320000-3344000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
4	chr4:3320400-3351800	Weak transcription	Aorta	Aorta
5	chr4:3321000-3347000	Weak transcription	Placenta Amnion	Placenta Amnion
6	chr4:3323600-3344000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
7	chr4:3323600-3344800	Weak transcription	Fetal Intestine Large	intestine
8	chr4:3324000-3341400	Weak transcription	Esophagus	oesophagus
9	chr4:3324000-3343600	Weak transcription	HSMM	muscle
10	chr4:3324200-3340200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
11	chr4:3324200-3342600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
12	chr4:3324200-3343600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
13	chr4:3325200-3342800	Weak transcription	Stomach Smooth Muscle	stomach
14	chr4:3325600-3348000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
15	chr4:3326200-3341800	Weak transcription	Brain Hippocampus Middle	brain
16	chr4:3326200-3342800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
17	chr4:3326400-3341200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
18	chr4:3326400-3341400	Weak transcription	Brain Angular Gyrus	brain
19	chr4:3326400-3343600	Weak transcription	Brain Inferior Temporal Lobe	brain
20	chr4:3326400-3343600	Weak transcription	NHLF	lung
21	chr4:3326400-3343800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
22	chr4:3326400-3344800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
23	chr4:3326400-3348000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
24	chr4:3328400-3343600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
25	chr4:3330200-3343600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
26	chr4:3331000-3343600	Weak transcription	Primary hematopoietic stem cells	blood
27	chr4:3331400-3339600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
28	chr4:3331400-3342400	Weak transcription	Psoas Muscle	Psoas
29	chr4:3332400-3343800	Weak transcription	Fetal Intestine Small	intestine
30	chr4:3332600-3342600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
31	chr4:3332800-3342000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
32	chr4:3332800-3342000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
33	chr4:3332800-3343600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
34	chr4:3332800-3343600	Weak transcription	Primary T cells from cord blood	blood
35	chr4:3332800-3343600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
36	chr4:3333600-3341800	Weak transcription	Gastric	stomach
37	chr4:3334000-3341800	Weak transcription	Skeletal Muscle Male	skeletal muscle
38	chr4:3334000-3342200	Weak transcription	Pancreas	Pancrea
39	chr4:3334000-3342400	Weak transcription	Left Ventricle	heart
40	chr4:3334000-3345800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
41	chr4:3334000-3370600	Weak transcription	Right Atrium	heart
42	chr4:3334400-3339600	Weak transcription	Spleen	Spleen
43	chr4:3334400-3341800	Weak transcription	Skeletal Muscle Female	skeletal muscle
44	chr4:3334400-3343600	Weak transcription	Adipose Nuclei	Adipose
45	chr4:3334600-3343600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
46	chr4:3336000-3341000	Enhancers	HUVEC	blood vessel
47	chr4:3336800-3340200	Weak transcription	Brain Germinal Matrix	brain
48	chr4:3337000-3344000	Weak transcription	Fetal Kidney	kidney
49	chr4:3337400-3340200	Weak transcription	Lung	lung
50	chr4:3337400-3343600	Weak transcription	Ovary	ovary

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