Variant report

Variant	nsv593453
Chromosome Location	chr4:3419840-3427972
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:171)
CpG islands
(count:674)
Chromatin interactive
region (count:10)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:171 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CEBPB	chr4:3423122-3423211	K562	blood:	n/a	n/a
2	CEBPB	chr4:3422746-3422943	Hela-S3	cervix:	n/a	n/a
3	CEBPB	chr4:3422619-3422819	HepG2	liver:	n/a	n/a
4	CEBPB	chr4:3422748-3422907	A549	lung:	n/a	n/a
5	CHD2	chr4:3420214-3420227	H1-hESC	embryonic stem cell:	n/a	n/a
6	CTCF	chr4:3420189-3420389	IMR90	lung:	n/a	n/a
7	CTCF	chr4:3420198-3420437	K562	blood:	n/a	n/a
8	CTCF	chr4:3420340-3420490	HepG2	liver:	n/a	n/a
9	CTCF	chr4:3420180-3420330	GM12878	blood:	n/a	n/a
10	CTCF	chr4:3420300-3420450	HCT-116	colon:	n/a	n/a
11	CTCF	chr4:3420200-3420350	GM12878	blood:	n/a	n/a
12	CTCF	chr4:3420214-3420436	Gliobla	brain:	n/a	n/a
13	CTCF	chr4:3420420-3420570	HFF-Myc	foreskin:	n/a	n/a
14	CTCF	chr4:3420300-3420450	AG04450	lung:	n/a	n/a
15	CTCF	chr4:3420171-3420444	K562	blood:	n/a	n/a
16	CTCF	chr4:3420400-3420550	HRE	kidney:	n/a	n/a
17	CTCF	chr4:3420300-3420450	RPTEC	kidney:	n/a	n/a
18	CTCF	chr4:3420240-3420390	GM12868	blood:	n/a	n/a
19	CTCF	chr4:3420280-3420430	HCT-116	colon:	n/a	n/a
20	CTCF	chr4:3420280-3420430	K562	blood:	n/a	n/a
21	CTCF	chr4:3420199-3420453	MCF-7	breast:	n/a	n/a
22	CTCF	chr4:3420280-3420430	HRE	kidney:	n/a	n/a
23	CTCF	chr4:3420320-3420470	AG10803	skin:	n/a	n/a
24	CTCF	chr4:3420260-3420410	GM12869	blood:	n/a	n/a
25	CTCF	chr4:3420320-3420470	SAEC	small airway:	n/a	n/a
26	CTCF	chr4:3420280-3420430	MCF-7	breast:	n/a	n/a
27	CTCF	chr4:3420240-3420390	SK-N-SH_RA	brain:	n/a	n/a
28	CTCF	chr4:3420260-3420410	HFF-Myc	foreskin:	n/a	n/a
29	CTCF	chr4:3420280-3420430	AG09319	gingival:	n/a	n/a
30	CTCF	chr4:3420309-3420359	Medullo	brain:	n/a	n/a
31	CTCF	chr4:3420201-3420461	NHEK	skin:	n/a	n/a
32	CTCF	chr4:3420300-3420450	HRPEpiC	eye:	n/a	n/a
33	CTCF	chr4:3420220-3420370	GM12864	blood:	n/a	n/a
34	CTCF	chr4:3420200-3420350	AG09319	gingival:	n/a	n/a
35	CTCF	chr4:3420260-3420410	WERI-Rb-1	eye:	n/a	n/a
36	CTCF	chr4:3420153-3420626	HCT-116	colon:	n/a	n/a
37	CTCF	chr4:3420240-3420390	GM12873	blood:	n/a	n/a
38	CTCF	chr4:3420220-3420370	NB4	blood:	n/a	n/a
39	CTCF	chr4:3420240-3420390	HBMEC	blood vessel:	n/a	n/a
40	CTCF	chr4:3420260-3420410	Caco-2	colon:	n/a	n/a
41	CTCF	chr4:3420260-3420410	HPAF	blood vessel:	n/a	n/a
42	CTCF	chr4:3420240-3420390	GM12874	blood:	n/a	n/a
43	CTCF	chr4:3420280-3420430	GM06990	blood:	n/a	n/a
44	CTCF	chr4:3420220-3420370	HCPEpiC	choroid plexus:	n/a	n/a
45	CTCF	chr4:3420237-3420403	Fibrobl	skin:	n/a	n/a
46	CTCF	chr4:3420158-3420492	H1-hESC	embryonic stem cell:	n/a	n/a
47	CTCF	chr4:3420220-3420370	HFF-Myc	foreskin:	n/a	n/a
48	CTCF	chr4:3420240-3420390	HMEC	breast:	n/a	n/a
49	CTCF	chr4:3420200-3420350	GM06990	blood:	n/a	n/a
50	CTCF	chr4:3420260-3420410	NHDF-neo	bronchial:	n/a	n/a

(count:674 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:3426363-3426413	NT2-D1	testis:	n/a
2	chr4:3424692-3424742	SAEC	small airway:	n/a
3	chr4:3425381-3425431	HNPCEpiC	eye:	n/a
4	chr4:3426363-3426413	NT2-D1	testis:	n/a
5	chr4:3424692-3424742	SAEC	small airway:	n/a
6	chr4:3425381-3425431	HNPCEpiC	eye:	n/a
7	chr4:3425962-3426012	NH-A	brain:	n/a
8	chr4:3424692-3424742	ovcar-3	ovarian:	n/a
9	chr4:3424470-3424520	LNCaP	prostate:	n/a
10	chr4:3425381-3425431	ProgFib	skin:	n/a
11	chr4:3424203-3424253	HL-60	blood:	n/a
12	chr4:3424692-3424742	BJ	skin:	n/a
13	chr4:3426363-3426413	AG10803	skin:	n/a
14	chr4:3425910-3425960	AG10803	skin:	n/a
15	chr4:3424470-3424520	MCF-7	breast:	n/a
16	chr4:3424470-3424520	NT2-D1	testis:	n/a
17	chr4:3425381-3425431	LNCaP	prostate:	n/a
18	chr4:3426534-3426584	ProgFib	skin:	n/a
19	chr4:3424470-3424520	SK-N-SH	brain:	n/a
20	chr4:3424692-3424742	HEEpiC	esophagus:	n/a
21	chr4:3426363-3426413	HL-60	blood:	n/a
22	chr4:3425381-3425431	PANC-1	pancreas:	n/a
23	chr4:3425910-3425960	Caco-2	colon:	n/a
24	chr4:3424470-3424520	AG09319	gingival:	n/a
25	chr4:3424203-3424253	PFSK-1	brain:	n/a
26	chr4:3425381-3425431	Hela-S3	cervix:	n/a
27	chr4:3426363-3426413	HCT-116	colon:	n/a
28	chr4:3426150-3426200	ProgFib	skin:	n/a
29	chr4:3424470-3424520	PANC-1	pancreas:	n/a
30	chr4:3425381-3425431	ECC-1	luminal epithelium:	n/a
31	chr4:3425910-3425960	ProgFib	skin:	n/a
32	chr4:3425910-3425960	GM12892	blood:	n/a
33	chr4:3425910-3425960	HEK293	kidney:	embryo
34	chr4:3426363-3426413	PANC-1	pancreas:	n/a
35	chr4:3425315-3425365	AG09319	gingival:	n/a
36	chr4:3424203-3424253	HPAEpiC	pulmonary alveolar:	n/a
37	chr4:3426534-3426584	Hela-S3	cervix:	n/a
38	chr4:3425962-3426012	NT2-D1	testis:	n/a
39	chr4:3424203-3424253	AG09319	gingival:	n/a
40	chr4:3424470-3424520	BE2_C	brain:	n/a
41	chr4:3425962-3426012	AG10803	skin:	n/a
42	chr4:3426534-3426584	AG10803	skin:	n/a
43	chr4:3425962-3426012	Caco-2	colon:	n/a
44	chr4:3425315-3425365	HepG2	liver:	n/a
45	chr4:3425910-3425960	NHBE	bronchial:	n/a
46	chr4:3426150-3426200	AG10803	skin:	n/a
47	chr4:3425910-3425960	NB4	blood:	n/a
48	chr4:3424692-3424742	PrEC	prostate:	n/a
49	chr4:3425381-3425431	HCF	heart:	n/a
50	chr4:3426150-3426200	K562	blood:	n/a

(count:10 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:3407565..3409961-chr4:3422127..3423905,2	K562	blood:
2	chr4:3416652..3419915-chr4:3441173..3444245,3	MCF-7	breast:
3	chr4:3419493..3422453-chr4:3423042..3425871,3	K562	blood:
4	chr4:3419493..3422453-chr4:3423042..3425871,3	K562	blood:
5	chr4:3422645..3425998-chr4:3426569..3431321,4	K562	blood:
6	chr4:3418487..3420284-chr4:3426920..3428463,2	K562	blood:
7	chr4:3422645..3425998-chr4:3426569..3431321,4	K562	blood:
8	chr4:3422937..3425880-chr4:3426569..3429789,3	K562	blood:
9	chr17:62399380..62400330-chr4:3422309..3422930,2	MCF-7	breast:
10	chr4:3418569..3420412-chr4:3484561..3487471,2	MCF-7	breast:

No data

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

Extended variants
information (count: 446 )
Associated
traits (count: 58 )

Variant overlapped rSNPs/rCNVs (count:446 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs12641989	chr4:3419840-3419841	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs144023392	chr4:3419845-3419846	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs537188974	chr4:3419859-3419860	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs150953012	chr4:3419860-3419861	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs140790905	chr4:3419866-3419867	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs554877996	chr4:3419913-3419914	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs185398542	chr4:3419954-3419955	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs553668395	chr4:3419955-3419956	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs16844316	chr4:3419970-3419971	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs190393786	chr4:3419973-3419974	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs743714	chr4:3419986-3419987	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
12	rs71608280	chr4:3420008-3420009	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs575647558	chr4:3420015-3420016	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs573546526	chr4:3420024-3420025	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs563896036	chr4:3420025-3420026	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs563129467	chr4:3420032-3420033	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs112081534	chr4:3420036-3420037	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs79348356	chr4:3420112-3420113	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs73792070	chr4:3420123-3420124	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs528394147	chr4:3420212-3420213	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs551166244	chr4:3420220-3420221	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs551077868	chr4:3420222-3420223	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs192074358	chr4:3420232-3420233	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs571266537	chr4:3420238-3420239	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs3748037	chr4:3420271-3420272	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs528437584	chr4:3420316-3420317	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs184085135	chr4:3420320-3420321	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs567383766	chr4:3420346-3420347	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs536812762	chr4:3420360-3420361	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs3748036	chr4:3420371-3420372	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs567043542	chr4:3420388-3420389	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs539367385	chr4:3420413-3420414	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs558660169	chr4:3420414-3420415	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs188473680	chr4:3420452-3420453	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs537862729	chr4:3420473-3420474	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs554613262	chr4:3420500-3420501	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs574592880	chr4:3420512-3420513	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs540928583	chr4:3420572-3420573	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs73193394	chr4:3420573-3420574	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs542375558	chr4:3420627-3420628	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs559165022	chr4:3420633-3420634	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs112173312	chr4:3420641-3420642	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs555486960	chr4:3420673-3420674	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs573053302	chr4:3420706-3420707	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs545316241	chr4:3420745-3420746	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs34799306	chr4:3420746-3420747	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs530493367	chr4:3420747-3420748	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs141399363	chr4:3420812-3420813	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs560918182	chr4:3420851-3420852	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs545533509	chr4:3420907-3420908	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:58)

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
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:285 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:3391800-3424200	Weak transcription	Colonic Mucosa	Colon
2	chr4:3399200-3432200	Weak transcription	Right Atrium	heart
3	chr4:3408800-3436600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
4	chr4:3411000-3436400	Strong transcription	Fetal Intestine Small	intestine
5	chr4:3411200-3436400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
6	chr4:3411200-3436600	Weak transcription	HUES6 Cell Line	embryonic stem cell
7	chr4:3411400-3425600	Weak transcription	H1 Cell Line	embryonic stem cell
8	chr4:3411800-3420000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
9	chr4:3413200-3420000	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
10	chr4:3413600-3437000	Strong transcription	Esophagus	oesophagus
11	chr4:3415000-3435600	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
12	chr4:3415000-3436400	Strong transcription	Cortex derived primary cultured neurospheres	brain
13	chr4:3415400-3437000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
14	chr4:3415600-3426000	Strong transcription	HepG2	liver
15	chr4:3415600-3433600	Weak transcription	Fetal Kidney	kidney
16	chr4:3415800-3421800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
17	chr4:3415800-3436400	Strong transcription	Lung	lung
18	chr4:3416000-3420600	Strong transcription	Right Ventricle	heart
19	chr4:3416200-3423000	Strong transcription	Fetal Stomach	stomach
20	chr4:3416400-3436200	Weak transcription	HUES48 Cell Line	embryonic stem cell
21	chr4:3416400-3436800	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
22	chr4:3416600-3423400	Weak transcription	Primary B cells from cord blood	blood
23	chr4:3416600-3423600	Weak transcription	Brain Angular Gyrus	brain
24	chr4:3416600-3428200	Weak transcription	Primary B cells from peripheral blood	blood
25	chr4:3416600-3435600	Strong transcription	Skeletal Muscle Male	skeletal muscle
26	chr4:3416600-3437800	Weak transcription	Stomach Mucosa	stomach
27	chr4:3416800-3420600	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
28	chr4:3416800-3420800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
29	chr4:3416800-3432000	Weak transcription	H9 Cell Line	embryonic stem cell
30	chr4:3416800-3436600	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
31	chr4:3416800-3438400	Weak transcription	NHDF-Ad	bronchial
32	chr4:3417000-3420600	Strong transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
33	chr4:3417000-3420600	Genic enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
34	chr4:3417000-3422800	Weak transcription	Fetal Thymus	thymus
35	chr4:3417200-3420000	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
36	chr4:3417200-3420400	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
37	chr4:3417200-3420600	Strong transcription	Fetal Lung	lung
38	chr4:3417200-3420600	Strong transcription	Gastric	stomach
39	chr4:3417200-3420600	Strong transcription	HSMMtube	muscle
40	chr4:3417200-3420800	Strong transcription	Pancreas	Pancrea
41	chr4:3417200-3420800	Strong transcription	HMEC	breast
42	chr4:3417200-3422600	Strong transcription	Sigmoid Colon	Sigmoid Colon
43	chr4:3417200-3427200	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
44	chr4:3417200-3433400	Strong transcription	Stomach Smooth Muscle	stomach
45	chr4:3417200-3435600	Strong transcription	Fetal Intestine Large	intestine
46	chr4:3417200-3444800	Weak transcription	Primary hematopoietic stem cells	blood
47	chr4:3417400-3420400	Strong transcription	Aorta	Aorta
48	chr4:3417400-3420800	Strong transcription	Brain Inferior Temporal Lobe	brain
49	chr4:3417400-3421400	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
50	chr4:3417400-3422400	Strong transcription	Duodenum Mucosa	Duodenum

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