Variant report

Variant	nsv593623
Chromosome Location	chr4:7991587-8012167
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	chr4:8011936-8012163	HepG2	liver:	n/a	n/a
2	BHLHE40	chr4:7998462-7998679	K562	blood:	n/a	n/a
3	BHLHE40	chr4:8002114-8002127	K562	blood:	n/a	n/a
4	CEBPB	chr4:7993736-7993804	K562	blood:	n/a	chr4:7993775-7993784 chr4:7993775-7993784 chr4:7993775-7993784 chr4:7993775-7993784
5	CEBPB	chr4:7993738-7993925	Hela-S3	cervix:	n/a	chr4:7993775-7993784 chr4:7993775-7993784 chr4:7993775-7993784 chr4:7993775-7993784
6	CEBPB	chr4:7993679-7993935	HepG2	liver:	n/a	chr4:7993775-7993784 chr4:7993775-7993784 chr4:7993775-7993784 chr4:7993775-7993784
7	CEBPB	chr4:7992893-7993178	IMR90	lung:	n/a	n/a
8	CEBPB	chr4:7992877-7993185	HepG2	liver:	n/a	n/a
9	CEBPB	chr4:7992907-7993072	Hela-S3	cervix:	n/a	n/a
10	CEBPB	chr4:7993614-7993933	A549	lung:	n/a	chr4:7993775-7993784 chr4:7993775-7993784 chr4:7993775-7993784 chr4:7993775-7993784
11	CEBPB	chr4:8011740-8011951	HepG2	liver:	n/a	chr4:8011839-8011850
12	CEBPB	chr4:7993645-7993940	IMR90	lung:	n/a	chr4:7993775-7993784 chr4:7993775-7993784 chr4:7993775-7993784 chr4:7993775-7993784
13	CTCF	chr4:7991480-7991630	BE2_C	brain:	n/a	n/a
14	CTCF	chr4:7995534-7995582	MCF-7	breast:	n/a	n/a
15	CTCF	chr4:7991641-7991691	GM12878	blood:	n/a	n/a
16	CTCF	chr4:7993940-7994090	WERI-Rb-1	eye:	n/a	n/a
17	CTCF	chr4:7995480-7995630	HUVEC	blood vessel:	n/a	n/a
18	CTCF	chr4:7995525-7995571	MCF-7	breast:	n/a	n/a
19	CTCF	chr4:7995400-7995550	GM06990	blood:	n/a	n/a
20	CTCF	chr4:7993340-7993490	SAEC	small airway:	n/a	n/a
21	CTCF	chr4:8008360-8008510	GM12866	blood:	n/a	chr4:8008476-8008489
22	E2F6	chr4:8007175-8007504	H1-hESC	embryonic stem cell:	n/a	n/a
23	E2F6	chr4:8007025-8007565	H1-hESC	embryonic stem cell:	n/a	n/a
24	EBF1	chr4:8010855-8011112	GM12878	blood:	n/a	chr4:8010996-8011006 chr4:8010995-8011006 chr4:8010995-8011008 chr4:8010997-8011006 chr4:8010997-8011006
25	EBF1	chr4:8007552-8007648	GM12878	blood:	n/a	chr4:8007614-8007627 chr4:8007616-8007625
26	EBF1	chr4:8010857-8011207	GM12878	blood:	n/a	chr4:8010996-8011006 chr4:8010995-8011006 chr4:8010995-8011008 chr4:8010997-8011006 chr4:8010997-8011006
27	EBF1	chr4:8010836-8011163	GM12878	blood:	n/a	chr4:8010996-8011006 chr4:8010995-8011006 chr4:8010995-8011008 chr4:8010997-8011006 chr4:8010997-8011006
28	ELF1	chr4:7995534-7995813	GM12878	blood:	n/a	n/a
29	EP300	chr4:8011785-8012292	MCF-7	breast:	n/a	n/a
30	EP300	chr4:8008115-8008525	MCF-7	breast:	n/a	n/a
31	EP300	chr4:8011809-8012234	MCF-7	breast:	n/a	n/a
32	ESR1	chr4:8011844-8012081	T-47D	breast:	n/a	chr4:8011979-8011996
33	ESR1	chr4:8011782-8012123	T-47D	breast:	n/a	chr4:8011979-8011996
34	ESR1	chr4:8011807-8012085	T-47D	breast:	n/a	chr4:8011979-8011996
35	ESR1	chr4:8011817-8012094	T-47D	breast:	n/a	chr4:8011979-8011996
36	FOXA1	chr4:8011795-8012195	HepG2	liver:	n/a	n/a
37	FOXA1	chr4:8011895-8012111	ECC-1	luminal epithelium:	n/a	n/a
38	FOXA1	chr4:8011805-8012197	HepG2	liver:	n/a	n/a
39	FOXA1	chr4:8011770-8012190	HepG2	liver:	n/a	n/a
40	FOXA2	chr4:8011861-8012086	HepG2	liver:	n/a	n/a
41	GATA3	chr4:8008005-8008638	MCF-7	breast:	n/a	n/a
42	GATA3	chr4:8011844-8012182	MCF-7	breast:	n/a	n/a
43	GATA3	chr4:8008013-8008581	MCF-7	breast:	n/a	n/a
44	GATA3	chr4:8008085-8008503	MCF-7	breast:	n/a	n/a
45	GATA3	chr4:8007860-8008911	MCF-7	breast:	n/a	n/a
46	HDAC2	chr4:8008095-8008603	MCF-7	breast:	n/a	n/a
47	HNF4A	chr4:8011446-8011737	HepG2	liver:	n/a	chr4:8011669-8011684
48	HNF4A	chr4:8011482-8011785	HepG2	liver:	n/a	chr4:8011669-8011684
49	MAX	chr4:8000243-8000572	MCF-7	breast:	n/a	n/a
50	MAX	chr4:8008135-8008591	MCF-7	breast:	n/a	chr4:8008290-8008299

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:8007014-8007064	BJ	skin:	n/a
2	chr4:8007156-8007206	HCT-116	colon:	n/a
3	chr4:8006893-8006943	GM19239	blood:	n/a
4	chr4:8007014-8007064	NT2-D1	testis:	n/a
5	chr4:8007156-8007206	RPTEC	kidney:	n/a
6	chr4:8007156-8007206	CMK	blood:	n/a
7	chr4:8007138-8007188	AoSMC	blood vessel:	n/a
8	chr4:8007014-8007064	NB4	blood:	n/a
9	chr4:8006893-8006943	HCT-116	colon:	n/a
10	chr4:8007014-8007064	HRPEpiC	eye:	n/a
11	chr4:8007138-8007188	NHBE	bronchial:	n/a
12	chr4:8007138-8007188	BJ	skin:	n/a
13	chr4:8007156-8007206	Hela-S3	cervix:	n/a
14	chr4:8006893-8006943	NHDF-neo	bronchial:	n/a
15	chr4:8007138-8007188	AG09319	gingival:	n/a
16	chr4:8006893-8006943	HAEpiC	amniotic membrane:	n/a
17	chr4:8007138-8007188	Jurkat	blood:	n/a
18	chr4:8007156-8007206	HCPEpiC	choroid plexus:	n/a
19	chr4:8007138-8007188	RPTEC	kidney:	n/a
20	chr4:8007138-8007188	ECC-1	luminal epithelium:	n/a
21	chr4:8007014-8007064	IMR90	lung:	fetal
22	chr4:8007014-8007064	HCPEpiC	choroid plexus:	n/a
23	chr4:8007156-8007206	HEK293	kidney:	embryo
24	chr4:8006893-8006943	ECC-1	luminal epithelium:	n/a
25	chr4:8007138-8007188	MCF-7	breast:	n/a
26	chr4:8009639-8009689	HMEC	breast:	n/a
27	chr4:8009639-8009689	PrEC	prostate:	n/a
28	chr4:8006893-8006943	HUVEC	blood vessel:	n/a
29	chr4:8009639-8009689	HCF	heart:	n/a
30	chr4:8006893-8006943	Hepatocyte	liver:	n/a
31	chr4:8009639-8009689	HRE	kidney:	n/a
32	chr4:8007156-8007206	AG09319	gingival:	n/a
33	chr4:8006893-8006943	HCPEpiC	choroid plexus:	n/a
34	chr4:8007014-8007064	ovcar-3	ovarian:	n/a
35	chr4:8009639-8009689	Jurkat	blood:	n/a
36	chr4:8006893-8006943	IMR90	lung:	fetal
37	chr4:8007014-8007064	GM12892	blood:	n/a
38	chr4:8007156-8007206	HNPCEpiC	eye:	n/a
39	chr4:8009639-8009689	RPTEC	kidney:	n/a
40	chr4:8007014-8007064	AG09309	skin:	n/a
41	chr4:8007156-8007206	T-47D	breast:	n/a
42	chr4:8007156-8007206	BJ	skin:	n/a
43	chr4:8007014-8007064	GM12891	blood:	n/a
44	chr4:8006893-8006943	SKMC	muscle:	n/a
45	chr4:8006893-8006943	AG09319	gingival:	n/a
46	chr4:8007156-8007206	PFSK-1	brain:	n/a
47	chr4:8006893-8006943	BE2_C	brain:	n/a
48	chr4:8007138-8007188	PrEC	prostate:	n/a
49	chr4:8007138-8007188	GM06990	blood:	n/a
50	chr4:8009639-8009689	PFSK-1	brain:	n/a

No.	Distal block	Cell Line	Cell type
1	chr4:7974598..7977296-chr4:7995967..7999387,3	MCF-7	breast:
2	chr4:7804324..7807098-chr4:7992889..7994621,2	MCF-7	breast:
3	chr4:8008264..8010463-chr4:8011198..8013869,4	MCF-7	breast:
4	chr4:7978137..7980891-chr4:8001316..8003240,2	MCF-7	breast:
5	chr4:8005982..8008973-chr4:8021942..8023511,2	MCF-7	breast:
6	chr4:7807434..7808952-chr4:8000439..8002438,2	MCF-7	breast:
7	chr4:8012081..8014539-chr4:8181803..8184689,2	MCF-7	breast:
8	chr4:8000666..8003023-chr4:8003232..8007313,4	MCF-7	breast:
9	chr4:7993971..7996546-chr4:8010581..8013516,2	MCF-7	breast:

miRNA name	Chromosome Location	mirBase accession
hsa-miR-95-3p	chr4:8007039-8007060	MIMAT0000094
hsa-miR-95-5p	chr4:8007074-8007094	MIMAT0026473

Variant related genes	Relation type
MIR95	TF binding region
MIR95	CpG island
ENSG00000125089	chromatin interactions
ENSG00000163995	chromatin interactions
ENSG00000207807	chromatin interactions
SNX1	Mature miRNA region

Extended variants
information (count: 967 )
Associated
traits (count: 53 )

Variant overlapped rSNPs/rCNVs (count:967 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4696662	chr4:7991587-7991588	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs553229775	chr4:7991600-7991601	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs192869403	chr4:7991605-7991606	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs535483983	chr4:7991626-7991627	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs115629752	chr4:7991646-7991647	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs184205051	chr4:7991660-7991661	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs575201157	chr4:7991661-7991662	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs16841536	chr4:7991669-7991670	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs187746029	chr4:7991674-7991675	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs573367296	chr4:7991686-7991687	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs540814833	chr4:7991724-7991725	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs559232278	chr4:7991735-7991736	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs529794923	chr4:7991739-7991740	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs368561057	chr4:7991748-7991749	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs371611911	chr4:7991804-7991805	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs73092305	chr4:7991846-7991847	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs371595352	chr4:7991856-7991857	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs371233013	chr4:7991882-7991883	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs192308336	chr4:7991908-7991909	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs552195513	chr4:7991926-7991927	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs114787265	chr4:7991949-7991950	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs528321791	chr4:7991958-7991959	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs546831627	chr4:7991966-7991967	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs568195752	chr4:7991984-7991985	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs183648777	chr4:7991985-7991986	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs188042577	chr4:7992049-7992050	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs375031317	chr4:7992058-7992059	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs550634570	chr4:7992071-7992072	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs146506382	chr4:7992102-7992103	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs539781282	chr4:7992107-7992108	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs192970182	chr4:7992164-7992165	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs184690745	chr4:7992183-7992184	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs115747998	chr4:7992204-7992205	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs76696765	chr4:7992223-7992224	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs554810474	chr4:7992252-7992253	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs373158024	chr4:7992403-7992404	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs375389542	chr4:7992425-7992426	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs541948031	chr4:7992433-7992434	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs374802548	chr4:7992436-7992437	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs537054722	chr4:7992444-7992445	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs372785311	chr4:7992456-7992457	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs369979647	chr4:7992487-7992488	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs113598830	chr4:7992506-7992507	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs76647925	chr4:7992546-7992547	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs76716504	chr4:7992619-7992620	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs4696726	chr4:7992632-7992633	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
47	rs546542497	chr4:7992663-7992664	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs190405618	chr4:7992709-7992710	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs369462660	chr4:7992734-7992735	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs13129405	chr4:7992749-7992750	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:53)

Disease	PMID	Source
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
Hodgkin''s lymphoma	17606441	CNVD
Prostate cancer	18632612	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Breast cancer	21785460	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Breast cancer	21509527	CNVD
Lung cancer	18438408	CNVD
Urothelial carcinoma	21177765	CNVD
Myelofibrosis	22110671	CNVD
Hirschsprung''s Disease	21712996	CNVD
Schizophrenia	22241247	CNVD
Autosomal-dominant microtia	18179897	CNVD
Glioma	17123091	CNVD
Colorectal cancer	20459617	CNVD
Breast cancer	17133270	CNVD
Breast cancer	22522925	CNVD
Sezary syndrome	18413736	CNVD

Chromatin state (count:237 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:7975800-8004800	Weak transcription	Brain Cingulate Gyrus	brain
2	chr4:7978800-8006000	Weak transcription	Brain Anterior Caudate	brain
3	chr4:7979600-8011400	Weak transcription	Pancreatic Islets	Pancreatic Islet
4	chr4:7981000-7992000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
5	chr4:7985400-8004800	Weak transcription	Brain Angular Gyrus	brain
6	chr4:7986800-7993600	Weak transcription	Brain Inferior Temporal Lobe	brain
7	chr4:7986800-8011400	Weak transcription	Rectal Mucosa Donor 29	rectum
8	chr4:7988000-7994200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
9	chr4:7988200-7993000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
10	chr4:7988200-7993600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
11	chr4:7988400-7992200	Weak transcription	Duodenum Mucosa	Duodenum
12	chr4:7988400-7993800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
13	chr4:7988400-8001200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
14	chr4:7988600-7996800	Weak transcription	Fetal Intestine Small	intestine
15	chr4:7989000-7993400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
16	chr4:7989800-8005800	Weak transcription	Psoas Muscle	Psoas
17	chr4:7990800-7991800	ZNF genes & repeats	Spleen	Spleen
18	chr4:7991400-7991600	ZNF genes & repeats	Brain Hippocampus Middle	brain
19	chr4:7991400-7991800	ZNF genes & repeats	Skeletal Muscle Female	skeletal muscle
20	chr4:7991400-7995200	Strong transcription	Skeletal Muscle Male	skeletal muscle
21	chr4:7991600-7991800	ZNF genes & repeats	Fetal Stomach	stomach
22	chr4:7991600-8006600	Weak transcription	Brain Hippocampus Middle	brain
23	chr4:7991800-7993000	Weak transcription	Spleen	Spleen
24	chr4:7991800-7994200	Weak transcription	Fetal Stomach	stomach
25	chr4:7991800-7995200	Strong transcription	Skeletal Muscle Female	skeletal muscle
26	chr4:7992000-7992200	ZNF genes & repeats	ES-WA7 Cell Line	embryonic stem cell
27	chr4:7992200-7992600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
28	chr4:7992800-7994200	Weak transcription	Brain Germinal Matrix	brain
29	chr4:7992800-8006600	Weak transcription	Aorta	Aorta
30	chr4:7993000-7994200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
31	chr4:7993000-7994600	Strong transcription	Spleen	Spleen
32	chr4:7993400-7995000	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
33	chr4:7993600-7994200	Strong transcription	Brain Inferior Temporal Lobe	brain
34	chr4:7993600-7994400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
35	chr4:7993800-7994400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
36	chr4:7994000-7994400	Enhancers	Cortex derived primary cultured neurospheres	brain
37	chr4:7994000-7995000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
38	chr4:7994200-7994400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
39	chr4:7994200-7994600	Enhancers	Brain Germinal Matrix	brain
40	chr4:7994200-7994600	Enhancers	Fetal Stomach	stomach
41	chr4:7994200-7994800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
42	chr4:7994200-8006000	Weak transcription	Brain Inferior Temporal Lobe	brain
43	chr4:7994400-7994600	Bivalent Enhancer	Fetal Muscle Trunk	muscle
44	chr4:7994400-7997400	Weak transcription	Cortex derived primary cultured neurospheres	brain
45	chr4:7994400-7997600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
46	chr4:7994600-7994800	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
47	chr4:7994600-7994800	Weak transcription	Spleen	Spleen
48	chr4:7994600-7995200	Enhancers	Breast Myoepithelial Primary Cells	Breast
49	chr4:7994600-7997000	Weak transcription	Fetal Stomach	stomach
50	chr4:7994800-7995200	Enhancers	Spleen	Spleen

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