Variant report

Variant	nsv877221
Chromosome Location	chr3:100546974-100592709
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:135)
CpG islands
(count:122)
Chromatin interactive
region (count:9)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:135 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr3:100549675-100549830	HepG2	liver:	n/a	n/a
2	ARID3A	chr3:100552318-100552684	HepG2	liver:	n/a	n/a
3	ATF1	chr3:100558200-100558457	K562	blood:	n/a	n/a
4	BATF	chr3:100562888-100563108	GM12878	blood:	n/a	chr3:100563023-100563034 chr3:100562983-100562994
5	BATF	chr3:100562933-100563097	GM12878	blood:	n/a	chr3:100563023-100563034 chr3:100562983-100562994
6	CEBPB	chr3:100576751-100577082	Hela-S3	cervix:	n/a	chr3:100576901-100576912
7	CEBPB	chr3:100576745-100577084	HepG2	liver:	n/a	chr3:100576901-100576912
8	CEBPB	chr3:100576769-100577008	A549	lung:	n/a	chr3:100576901-100576912
9	CEBPB	chr3:100579754-100579849	H1-hESC	embryonic stem cell:	n/a	chr3:100579783-100579794
10	CEBPB	chr3:100576787-100576939	H1-hESC	embryonic stem cell:	n/a	chr3:100576901-100576912
11	CEBPB	chr3:100579621-100579953	HepG2	liver:	n/a	chr3:100579783-100579794
12	CEBPB	chr3:100579666-100579935	K562	blood:	n/a	chr3:100579783-100579794
13	CEBPB	chr3:100576764-100577040	IMR90	lung:	n/a	chr3:100576901-100576912
14	CEBPB	chr3:100579710-100579958	A549	lung:	n/a	chr3:100579783-100579794
15	CEBPB	chr3:100579621-100579958	IMR90	lung:	n/a	chr3:100579783-100579794
16	CEBPB	chr3:100576786-100577007	K562	blood:	n/a	chr3:100576901-100576912
17	CHD2	chr3:100546937-100547089	K562	blood:	n/a	chr3:100546973-100546982
18	CTCF	chr3:100565460-100565610	HRE	kidney:	n/a	n/a
19	CTCF	chr3:100575829-100575923	Hela-S3	cervix:	n/a	n/a
20	CTCF	chr3:100589540-100589690	Caco-2	colon:	n/a	n/a
21	CTCF	chr3:100592280-100592430	GM12867	blood:	n/a	n/a
22	CTCF	chr3:100575520-100575670	HRPEpiC	eye:	n/a	n/a
23	E2F4	chr3:100585238-100585299	MCF10A-Er-Src	breast:	n/a	n/a
24	E2F4	chr3:100583009-100583138	MCF10A-Er-Src	breast:	n/a	n/a
25	E2F6	chr3:100549889-100550209	H1-hESC	embryonic stem cell:	n/a	n/a
26	ELF1	chr3:100558021-100558287	K562	blood:	n/a	chr3:100558183-100558196 chr3:100558185-100558196
27	EP300	chr3:100588555-100589044	T-47D	breast:	n/a	chr3:100588680-100588694 chr3:100588678-100588687
28	EP300	chr3:100552303-100552709	HepG2	liver:	n/a	n/a
29	EP300	chr3:100583633-100584767	T-47D	breast:	n/a	chr3:100584396-100584410 chr3:100584472-100584482
30	EP300	chr3:100552283-100552760	SK-N-SH_RA	brain:	n/a	n/a
31	EP300	chr3:100584175-100584646	T-47D	breast:	n/a	chr3:100584396-100584410 chr3:100584472-100584482
32	EP300	chr3:100552275-100552825	SK-N-SH_RA	brain:	n/a	n/a
33	EP300	chr3:100550384-100550854	T-47D	breast:	n/a	n/a
34	EP300	chr3:100588468-100589107	T-47D	breast:	n/a	chr3:100588680-100588694 chr3:100588678-100588687
35	EP300	chr3:100552428-100552824	HepG2	liver:	n/a	n/a
36	EP300	chr3:100553970-100554312	SK-N-SH_RA	brain:	n/a	n/a
37	EP300	chr3:100550343-100551031	T-47D	breast:	n/a	n/a
38	ESR1	chr3:100584248-100584695	T-47D	breast:	n/a	n/a
39	ESR1	chr3:100583661-100584591	T-47D	breast:	n/a	chr3:100583965-100583982
40	ESR1	chr3:100588619-100589055	T-47D	breast:	n/a	n/a
41	ESR1	chr3:100583631-100584206	T-47D	breast:	n/a	chr3:100583965-100583982
42	ESR1	chr3:100584191-100584716	T-47D	breast:	n/a	n/a
43	ESR1	chr3:100583816-100584125	T-47D	breast:	n/a	chr3:100583965-100583982
44	ESR1	chr3:100583725-100584574	T-47D	breast:	n/a	chr3:100583965-100583982
45	ESR1	chr3:100588637-100589069	T-47D	breast:	n/a	n/a
46	ESR1	chr3:100583685-100584154	T-47D	breast:	n/a	chr3:100583965-100583982
47	ESR1	chr3:100588584-100588969	T-47D	breast:	n/a	n/a
48	ESR1	chr3:100583784-100584680	T-47D	breast:	n/a	chr3:100583965-100583982
49	FAM48A	chr3:100573621-100573687	GM12878	blood:	n/a	n/a
50	FOS	chr3:100588700-100588916	MCF10A-Er-Src	breast:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:100560402-100560452	T-47D	breast:	n/a
2	chr3:100560402-100560452	K562	blood:	n/a
3	chr3:100559884-100559934	SK-N-SH	brain:	n/a
4	chr3:100560402-100560452	HRPEpiC	eye:	n/a
5	chr3:100560402-100560452	MCF10A-Er-Src	breast:	n/a
6	chr3:100560402-100560452	NH-A	brain:	n/a
7	chr3:100559884-100559934	HRE	kidney:	n/a
8	chr3:100560402-100560452	AG09319	gingival:	n/a
9	chr3:100559884-100559934	PFSK-1	brain:	n/a
10	chr3:100560402-100560452	HCF	heart:	n/a
11	chr3:100559884-100559934	HCT-116	colon:	n/a
12	chr3:100560402-100560452	HRE	kidney:	n/a
13	chr3:100560402-100560452	GM19239	blood:	n/a
14	chr3:100559884-100559934	SKMC	muscle:	n/a
15	chr3:100560402-100560452	Jurkat	blood:	n/a
16	chr3:100559884-100559934	HNPCEpiC	eye:	n/a
17	chr3:100560402-100560452	NHDF-neo	bronchial:	n/a
18	chr3:100560402-100560452	PANC-1	pancreas:	n/a
19	chr3:100559884-100559934	GM12878	blood:	n/a
20	chr3:100560402-100560452	HL-60	blood:	n/a
21	chr3:100560402-100560452	AG10803	skin:	n/a
22	chr3:100559884-100559934	K562	blood:	n/a
23	chr3:100560402-100560452	ProgFib	skin:	n/a
24	chr3:100560402-100560452	HPAEpiC	pulmonary alveolar:	n/a
25	chr3:100559884-100559934	GM12891	blood:	n/a
26	chr3:100560402-100560452	AG04450	lung:	fetal
27	chr3:100559884-100559934	HCF	heart:	n/a
28	chr3:100560402-100560452	Hepatocyte	liver:	n/a
29	chr3:100560402-100560452	Caco-2	colon:	n/a
30	chr3:100559884-100559934	PANC-1	pancreas:	n/a
31	chr3:100559884-100559934	A549	lung:	n/a
32	chr3:100560402-100560452	HCM	heart:	n/a
33	chr3:100559884-100559934	AG09309	skin:	n/a
34	chr3:100559884-100559934	T-47D	breast:	n/a
35	chr3:100560402-100560452	HUVEC	blood vessel:	n/a
36	chr3:100560402-100560452	HCPEpiC	choroid plexus:	n/a
37	chr3:100559884-100559934	SK-N-SH_RA	brain:	n/a
38	chr3:100559884-100559934	BJ	skin:	n/a
39	chr3:100559884-100559934	PrEC	prostate:	n/a
40	chr3:100560402-100560452	MCF-7	breast:	n/a
41	chr3:100559884-100559934	AG10803	skin:	n/a
42	chr3:100560402-100560452	AoSMC	blood vessel:	n/a
43	chr3:100560402-100560452	HRCEpiC	kidney:	n/a
44	chr3:100559884-100559934	HRPEpiC	eye:	n/a
45	chr3:100559884-100559934	NT2-D1	testis:	n/a
46	chr3:100559884-100559934	NHDF-neo	bronchial:	n/a
47	chr3:100559884-100559934	HAEpiC	amniotic membrane:	n/a
48	chr3:100560402-100560452	HepG2	liver:	n/a
49	chr3:100559884-100559934	NB4	blood:	n/a
50	chr3:100560402-100560452	SAEC	small airway:	n/a

(count:9 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr3:100562189..100564095-chr3:100566373..100568279,2	K562	blood:
2	chr3:100583637..100584415-chr3:100593364..100593885,2	MCF-7	breast:
3	chr3:100548174..100550868-chr3:100558389..100562132,3	K562	blood:
4	chr3:100570294..100571899-chr3:100575158..100577343,2	MCF-7	breast:
5	chr3:100566339..100567938-chr3:100570084..100572693,2	K562	blood:
6	chr3:100570294..100571899-chr3:100575158..100577343,2	MCF-7	breast:
7	chr3:100583616..100584474-chr3:100593349..100593875,2	MCF-7	breast:
8	chr3:100552627..100555196-chr3:100557683..100559579,2	K562	blood:
9	chr3:100579928..100582601-chr3:100582834..100585317,2	K562	blood:

(count:6 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-IMPG2-3	chr3:100553528-100553617	NONHSAT090880
2	lnc-IMPG2-3	chr3:100551969-100552001	NONHSAT090880
3	lnc-IMPG2-3	chr3:100551108-100551194	NONHSAT090880
4	lnc-IMPG2-3	chr3:100549422-100549478	NONHSAT090880
5	lnc-IMPG2-3	chr3:100555968-100556167	NONHSAT090880
6	lnc-IMPG2-3	chr3:100554445-100554504	NONHSAT090880

No data

Variant related genes	Relation type
ABI3BP	TF binding region
ABI3BP	CpG island
ENSG00000154175	chromatin interactions

Extended variants
information (count: 1686 )
Associated
traits (count: 56 )

Variant overlapped rSNPs/rCNVs (count:1686 , 50 per page) page: 1 2 3 4 5 6 7 ... 34

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs13076717	chr3:100546974-100546975	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	mRNA abundance
2	rs150411282	chr3:100546977-100546978	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs9862495	chr3:100546978-100546979	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs574382222	chr3:100546979-100546980	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs550013654	chr3:100546996-100546997	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs541669508	chr3:100547023-100547024	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs556717132	chr3:100547042-100547043	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs575368304	chr3:100547080-100547081	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs12107754	chr3:100547137-100547138	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs564528343	chr3:100547138-100547139	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs75247355	chr3:100547149-100547150	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs549102198	chr3:100547221-100547222	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs143322195	chr3:100547238-100547239	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs527415180	chr3:100547291-100547292	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs561346759	chr3:100547363-100547364	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs182550645	chr3:100547377-100547378	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs73135573	chr3:100547378-100547379	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs550485481	chr3:100547405-100547406	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs551222291	chr3:100547486-100547487	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs188062053	chr3:100547497-100547498	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs530644766	chr3:100547504-100547505	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs370944922	chr3:100547522-100547523	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs551570634	chr3:100547528-100547529	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs570429789	chr3:100547600-100547601	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs534361572	chr3:100547651-100547652	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs546185053	chr3:100547667-100547668	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs568042970	chr3:100547691-100547692	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs535348998	chr3:100547769-100547770	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs568842114	chr3:100547773-100547774	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs556755868	chr3:100547795-100547796	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs191813956	chr3:100547824-100547825	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs376973416	chr3:100547837-100547838	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs117453175	chr3:100547850-100547851	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs573275218	chr3:100547937-100547938	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs201153906	chr3:100547983-100547984	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs56338787	chr3:100547984-100547985	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	mRNA abundance
37	rs58672723	chr3:100547985-100547986	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs562039464	chr3:100547995-100547996	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs80288315	chr3:100547996-100547997	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs77211546	chr3:100547997-100547998	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs56140308	chr3:100547998-100547999	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	mRNA abundance
42	rs72932521	chr3:100548018-100548019	Strong transcription Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs563096678	chr3:100548041-100548042	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs533824407	chr3:100548090-100548091	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs138966607	chr3:100548104-100548105	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs552258119	chr3:100548120-100548121	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs551594239	chr3:100548142-100548143	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs564074745	chr3:100548198-100548199	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs184101559	chr3:100548214-100548215	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs546224858	chr3:100548225-100548226	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:56)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Glioblastoma multiforme	21080181	CNVD
Retinoblastoma	21504564	CNVD
Renal cell carcinoma	21668985	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	17603634	CNVD
Uveal melanoma	20484589	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
Hirschsprung''s Disease	21712996	CNVD
Hepatocellular carcinoma	16750200	CNVD
Cancer	21183584	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Bipolar disorder	20877625	CNVD
Bipolar disorder	21956041	CNVD
Bipolar disorder	22241247	CNVD
Biliary cancer	18923514	CNVD
Prostate cancer	21965145	CNVD
Cancer	21129771	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Cervical cancer	21062161	CNVD
Squamous cell cancer	20885788	CNVD
Melanoma	18172304	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Bipolar disorder	18458673	CNVD
Breast cancer	22032731	CNVD
Neurodevelopmental disorder	22521361	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Breast cancer	16461572	CNVD
Neuroblastoma	17533364	CNVD
microdeletion syndrome	22180640	CNVD
Cervical Cancer	21857958	CNVD
Melanoma	21693616	CNVD
Lung cancer	21426551	CNVD
Cancer	21637783	CNVD
Cervical cancer	21063398	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Oral cancer	21386901	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	22065749	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
small cell lung cancer	20016488	CNVD
Ductal carcinoma	22052326	CNVD
Myelofibrosis	22110671	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Breast cancer	16608533	CNVD
Breast cancer	21785460	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD

Chromatin state (count:288 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:100505200-100558200	Weak transcription	Ovary	ovary
2	chr3:100505200-100582800	Weak transcription	Fetal Muscle Trunk	muscle
3	chr3:100506000-100548400	Weak transcription	Stomach Smooth Muscle	stomach
4	chr3:100514200-100547600	Weak transcription	Fetal Muscle Leg	muscle
5	chr3:100516000-100572200	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
6	chr3:100517400-100594400	Weak transcription	Duodenum Smooth Muscle	Duodenum
7	chr3:100530000-100594400	Weak transcription	HSMM	muscle
8	chr3:100530400-100547000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
9	chr3:100530800-100555400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
10	chr3:100531600-100555400	Weak transcription	NHDF-Ad	bronchial
11	chr3:100533800-100573000	Weak transcription	Aorta	Aorta
12	chr3:100538000-100547800	Weak transcription	Muscle Satellite Cultured Cells	--
13	chr3:100539000-100558200	Weak transcription	Rectal Smooth Muscle	rectum
14	chr3:100541600-100547000	Weak transcription	HSMMtube	muscle
15	chr3:100543800-100547800	Weak transcription	Fetal Stomach	stomach
16	chr3:100544800-100547600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
17	chr3:100545600-100554400	Strong transcription	Osteobl	bone
18	chr3:100547000-100548800	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
19	chr3:100547000-100553800	Strong transcription	HSMMtube	muscle
20	chr3:100547000-100555600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
21	chr3:100547600-100547800	Enhancers	Lung	lung
22	chr3:100547600-100550600	Strong transcription	Fetal Muscle Leg	muscle
23	chr3:100547600-100553800	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
24	chr3:100547800-100548600	Strong transcription	Muscle Satellite Cultured Cells	--
25	chr3:100547800-100548600	Strong transcription	Fetal Stomach	stomach
26	chr3:100548400-100552400	Strong transcription	Stomach Smooth Muscle	stomach
27	chr3:100548600-100555400	Weak transcription	Muscle Satellite Cultured Cells	--
28	chr3:100548600-100558200	Weak transcription	Fetal Stomach	stomach
29	chr3:100548800-100549400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
30	chr3:100549400-100549600	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
31	chr3:100549400-100563000	Weak transcription	Fetal Lung	lung
32	chr3:100549600-100550000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
33	chr3:100549800-100562200	Weak transcription	Fetal Intestine Large	intestine
34	chr3:100550000-100550200	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
35	chr3:100550200-100555200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
36	chr3:100550600-100558000	Weak transcription	Fetal Muscle Leg	muscle
37	chr3:100551800-100553200	Enhancers	HepG2	liver
38	chr3:100551800-100553400	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin03	Skin
39	chr3:100552000-100552800	Enhancers	Brain Substantia Nigra	brain
40	chr3:100552000-100553400	Enhancers	Brain Hippocampus Middle	brain
41	chr3:100552000-100553600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
42	chr3:100552400-100553000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
43	chr3:100552400-100553000	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
44	chr3:100552400-100557800	Weak transcription	Stomach Smooth Muscle	stomach
45	chr3:100552600-100553000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
46	chr3:100552600-100553000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
47	chr3:100552600-100553000	Enhancers	Brain Inferior Temporal Lobe	brain
48	chr3:100552600-100553600	Enhancers	Brain Angular Gyrus	brain
49	chr3:100552800-100553000	Enhancers	Brain Anterior Caudate	brain
50	chr3:100552800-100553000	Flanking Active TSS	Brain Substantia Nigra	brain

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