Variant report

Variant	esv3445327
Chromosome Location	chr3:121260311-121288302
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	chr3:121264757-121265250	HepG2	liver:	n/a	n/a
2	ARID3A	chr3:121264632-121265235	K562	blood:	n/a	n/a
3	ARID3A	chr3:121265453-121265941	HepG2	liver:	n/a	n/a
4	ARID3A	chr3:121265480-121265882	K562	blood:	n/a	n/a
5	ATF2	chr3:121264561-121265245	GM12878	blood:	n/a	n/a
6	ATF2	chr3:121267420-121267944	GM12878	blood:	n/a	n/a
7	ATF2	chr3:121267479-121267985	GM12878	blood:	n/a	n/a
8	ATF2	chr3:121264597-121265169	GM12878	blood:	n/a	n/a
9	ATF2	chr3:121265572-121266011	H1-hESC	embryonic stem cell:	n/a	n/a
10	ATF3	chr3:121264594-121265142	A549	lung:	n/a	chr3:121264846-121264855
11	BATF	chr3:121267535-121267976	GM12878	blood:	n/a	n/a
12	BATF	chr3:121267576-121267909	GM12878	blood:	n/a	n/a
13	BCL3	chr3:121271688-121271931	GM12878	blood:	n/a	n/a
14	BCLAF1	chr3:121264518-121265140	GM12878	blood:	n/a	n/a
15	BCLAF1	chr3:121264580-121265251	GM12878	blood:	n/a	n/a
16	BCLAF1	chr3:121267517-121268093	GM12878	blood:	n/a	n/a
17	BHLHE40	chr3:121267547-121267919	GM12878	blood:	n/a	n/a
18	BHLHE40	chr3:121264738-121264916	K562	blood:	n/a	n/a
19	BHLHE40	chr3:121264707-121265217	GM12878	blood:	n/a	n/a
20	BRCA1	chr3:121264554-121265265	Hela-S3	cervix:	n/a	n/a
21	CBX3	chr3:121264666-121265161	K562	blood:	n/a	chr3:121265149-121265160
22	CCNT2	chr3:121264449-121264875	K562	blood:	n/a	n/a
23	CEBPB	chr3:121261830-121262092	A549	lung:	n/a	chr3:121261903-121261914
24	CEBPB	chr3:121261870-121262080	H1-hESC	embryonic stem cell:	n/a	chr3:121261903-121261914
25	CEBPB	chr3:121264706-121265963	IMR90	lung:	n/a	chr3:121265493-121265506 chr3:121265176-121265189 chr3:121265495-121265506
26	CEBPB	chr3:121264666-121266054	MCF-7	breast:	n/a	chr3:121265493-121265506 chr3:121265176-121265189 chr3:121265495-121265506
27	CEBPB	chr3:121264766-121266044	ECC-1	luminal epithelium:	n/a	chr3:121265493-121265506 chr3:121265176-121265189 chr3:121265495-121265506
28	CEBPB	chr3:121265311-121265997	ECC-1	luminal epithelium:	n/a	chr3:121265493-121265506 chr3:121265495-121265506
29	CEBPB	chr3:121261808-121262108	A549	lung:	n/a	chr3:121261903-121261914
30	CEBPB	chr3:121261830-121262067	K562	blood:	n/a	chr3:121261903-121261914
31	CEBPB	chr3:121264701-121265053	K562	blood:	n/a	n/a
32	CEBPB	chr3:121284914-121285076	HepG2	liver:	n/a	chr3:121284967-121284978
33	CEBPB	chr3:121264670-121266056	A549	lung:	n/a	chr3:121265493-121265506 chr3:121265176-121265189 chr3:121265495-121265506
34	CEBPB	chr3:121264621-121266051	GM12878	blood:	n/a	chr3:121265493-121265506 chr3:121265176-121265189 chr3:121265495-121265506
35	CEBPB	chr3:121265317-121265984	HCT-116	colon:	n/a	chr3:121265493-121265506 chr3:121265495-121265506
36	CEBPB	chr3:121261827-121262080	HepG2	liver:	n/a	chr3:121261903-121261914
37	CEBPB	chr3:121264581-121266055	HCT-116	colon:	n/a	chr3:121265493-121265506 chr3:121265176-121265189 chr3:121265495-121265506
38	CEBPB	chr3:121265383-121265914	K562	blood:	n/a	chr3:121265493-121265506 chr3:121265495-121265506
39	CEBPB	chr3:121264701-121265949	A549	lung:	n/a	chr3:121265493-121265506 chr3:121265176-121265189 chr3:121265495-121265506
40	CEBPB	chr3:121264724-121265949	HepG2	liver:	n/a	chr3:121265493-121265506 chr3:121265176-121265189 chr3:121265495-121265506
41	CEBPB	chr3:121265292-121265994	K562	blood:	n/a	chr3:121265493-121265506 chr3:121265495-121265506
42	CEBPB	chr3:121264638-121265967	Hela-S3	cervix:	n/a	chr3:121265493-121265506 chr3:121265176-121265189 chr3:121265495-121265506
43	CEBPB	chr3:121265347-121265933	HepG2	liver:	n/a	chr3:121265493-121265506 chr3:121265495-121265506
44	CEBPB	chr3:121264767-121265991	A549	lung:	n/a	chr3:121265493-121265506 chr3:121265176-121265189 chr3:121265495-121265506
45	CEBPB	chr3:121264671-121265977	MCF-7	breast:	n/a	chr3:121265493-121265506 chr3:121265176-121265189 chr3:121265495-121265506
46	CEBPB	chr3:121261734-121262093	IMR90	lung:	n/a	chr3:121261903-121261914
47	CEBPB	chr3:121265619-121265862	HepG2	liver:	n/a	n/a
48	CEBPB	chr3:121279914-121280356	Hela-S3	cervix:	n/a	n/a
49	CEBPB	chr3:121265352-121265933	HepG2	liver:	n/a	chr3:121265493-121265506 chr3:121265495-121265506
50	CEBPB	chr3:121265309-121265961	H1-hESC	embryonic stem cell:	n/a	chr3:121265493-121265506 chr3:121265495-121265506

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:121287348-121287398	HEK293	kidney:	embryo
2	chr3:121264903-121264953	LNCaP	prostate:	n/a
3	chr3:121285706-121285756	HPAEpiC	pulmonary alveolar:	n/a
4	chr3:121286354-121286404	AoSMC	blood vessel:	n/a
5	chr3:121264693-121264743	AG09319	gingival:	n/a
6	chr3:121286563-121286613	AoSMC	blood vessel:	n/a
7	chr3:121264278-121264328	SK-N-SH	brain:	n/a
8	chr3:121264903-121264953	HCM	heart:	n/a
9	chr3:121264942-121264992	MCF10A-Er-Src	breast:	n/a
10	chr3:121265395-121265445	HMEC	breast:	n/a
11	chr3:121285779-121285829	SKMC	muscle:	n/a
12	chr3:121286563-121286613	HEK293	kidney:	embryo
13	chr3:121286354-121286404	U87	brain:	n/a
14	chr3:121286820-121286870	PFSK-1	brain:	n/a
15	chr3:121264903-121264953	AG10803	skin:	n/a
16	chr3:121262243-121262293	SAEC	small airway:	n/a
17	chr3:121286820-121286870	T-47D	breast:	n/a
18	chr3:121265726-121265776	CMK	blood:	n/a
19	chr3:121264929-121264979	HEK293	kidney:	embryo
20	chr3:121264819-121264869	PFSK-1	brain:	n/a
21	chr3:121286563-121286613	NB4	blood:	n/a
22	chr3:121264819-121264869	ovcar-3	ovarian:	n/a
23	chr3:121264201-121264251	HEEpiC	esophagus:	n/a
24	chr3:121264929-121264979	AG09319	gingival:	n/a
25	chr3:121262243-121262293	HL-60	blood:	n/a
26	chr3:121264903-121264953	BJ	skin:	n/a
27	chr3:121262243-121262293	GM12878	blood:	n/a
28	chr3:121264923-121264973	IMR90	lung:	fetal
29	chr3:121267733-121267783	HEK293	kidney:	embryo
30	chr3:121264849-121264899	AoSMC	blood vessel:	n/a
31	chr3:121286354-121286404	HIPEpiC	eye:	n/a
32	chr3:121286563-121286613	PFSK-1	brain:	n/a
33	chr3:121264942-121264992	GM12892	blood:	n/a
34	chr3:121280760-121280810	HUVEC	blood vessel:	n/a
35	chr3:121264844-121264894	NHDF-neo	bronchial:	n/a
36	chr3:121286563-121286613	HRPEpiC	eye:	n/a
37	chr3:121262503-121262553	AG09309	skin:	n/a
38	chr3:121286820-121286870	HMEC	breast:	n/a
39	chr3:121264942-121264992	HNPCEpiC	eye:	n/a
40	chr3:121287348-121287398	HEEpiC	esophagus:	n/a
41	chr3:121280760-121280810	SK-N-SH	brain:	n/a
42	chr3:121264844-121264894	NH-A	brain:	n/a
43	chr3:121264903-121264953	HCT-116	colon:	n/a
44	chr3:121286563-121286613	GM19239	blood:	n/a
45	chr3:121286354-121286404	K562	blood:	n/a
46	chr3:121264844-121264894	AG10803	skin:	n/a
47	chr3:121264903-121264953	AG09309	skin:	n/a
48	chr3:121286820-121286870	Hepatocyte	liver:	n/a
49	chr3:121287348-121287398	HIPEpiC	eye:	n/a
50	chr3:121285779-121285829	U87	brain:	n/a

No.	Distal block	Cell Line	Cell type
1	chr3:121259538..121263018-chr3:121263022..121266683,5	K562	blood:
2	chr3:121264864..121267091-chr3:122101354..122103102,2	MCF-7	breast:
3	chr3:121257218..121258726-chr3:121258912..121261843,2	K562	blood:
4	chr3:121264895..121265445-chr3:121468081..121468931,2	HCT-116	colon:
5	chr3:121264432..121265085-chr8:141467270..141468232,2	Hela-S3	cervix:
6	chr3:121265150..121267222-chr3:121267374..121269393,2	K562	blood:
7	chr3:121263813..121266298-chr3:122398939..122401596,2	K562	blood:
8	chr3:121256811..121260221-chr3:121262363..121264764,4	MCF-7	breast:
9	chr3:121261975..121264944-chr3:121467360..121470216,3	K562	blood:
10	chr3:121265303..121265930-chr3:121811130..121811872,2	MCF-7	breast:
11	chr3:121271397..121273219-chr3:122101468..122103033,2	K562	blood:
12	chr3:121264525..121266753-chr3:121273647..121275998,2	K562	blood:
13	chr3:121262548..121264431-chr3:121401420..121403788,2	K562	blood:
14	chr3:121264839..121267237-chr3:122281910..122284575,2	MCF-7	breast:
15	chr1:145382746..145383629-chr3:121264432..121265003,2	Hela-S3	cervix:
16	chr3:121262393..121265271-chr3:121277271..121279560,2	MCF-7	breast:
17	chr3:121265150..121267222-chr3:121267374..121269393,2	K562	blood:
18	chr3:121264298..121266034-chr3:122100794..122102974,2	MCF-7	breast:
19	chr3:121257674..121260535-chr3:121261894..121265462,3	MCF-7	breast:
20	chr3:121249276..121252211-chr3:121260575..121262874,2	MCF-7	breast:
21	chr3:121265697..121266207-chr3:122977401..122978341,2	K562	blood:
22	chr3:121263260..121265570-chr3:121468289..121470216,2	K562	blood:
23	chr3:121263491..121265604-chr3:121269317..121270972,2	K562	blood:

Variant related genes	Relation type
POLQ	TF binding region
ARGFX	TF binding region
POLQ	CpG island
ARGFX	CpG island
ENSG00000160124	chromatin interactions
ENSG00000138496	chromatin interactions
ENSG00000051341	chromatin interactions
ENSG00000173193	chromatin interactions
ENSG00000114023	chromatin interactions
ENSG00000173230	chromatin interactions
ENSG00000167632	chromatin interactions
ENSG00000163840	chromatin interactions
ENSG00000201558	chromatin interactions

Extended variants
information (count: 1142 )
Associated
traits (count: 64 )

Variant overlapped rSNPs/rCNVs (count:1142 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs370074954	chr3:121260315-121260316	Strong transcription Weak transcription Genic enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs141638362	chr3:121260325-121260326	Strong transcription Weak transcription Genic enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs75509410	chr3:121260372-121260373	Strong transcription Weak transcription Genic enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs183249693	chr3:121260373-121260374	Strong transcription Weak transcription Genic enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs543929187	chr3:121260404-121260405	Strong transcription Weak transcription Genic enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs187858444	chr3:121260450-121260451	Strong transcription Weak transcription Genic enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs554562720	chr3:121260456-121260457	Strong transcription Weak transcription Genic enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs538097550	chr3:121260491-121260492	Strong transcription Weak transcription Genic enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs55769719	chr3:121260496-121260497	Strong transcription Weak transcription Genic enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs559998201	chr3:121260537-121260538	Strong transcription Weak transcription Genic enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs566958258	chr3:121260580-121260581	Strong transcription Weak transcription Genic enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs532214501	chr3:121260584-121260585	Strong transcription Weak transcription Genic enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs192692864	chr3:121260649-121260650	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs545590805	chr3:121260690-121260691	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs552299911	chr3:121260703-121260704	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs562498576	chr3:121260709-121260710	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs138727117	chr3:121260714-121260715	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs184454086	chr3:121260717-121260718	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs557688675	chr3:121260729-121260730	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs529632382	chr3:121260736-121260737	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs142778003	chr3:121260784-121260785	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs147401964	chr3:121260798-121260799	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs577729928	chr3:121260804-121260805	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs549712214	chr3:121260814-121260815	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs74714617	chr3:121260824-121260825	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs548145105	chr3:121260851-121260852	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs571152430	chr3:121260852-121260853	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs13095550	chr3:121260897-121260898	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs556803788	chr3:121260906-121260907	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs187638702	chr3:121260907-121260908	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs200039715	chr3:121260911-121260912	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs554345273	chr3:121260916-121260917	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs538835400	chr3:121260926-121260927	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs34442880	chr3:121260960-121260961	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs367776728	chr3:121260977-121260978	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs558432305	chr3:121260978-121260979	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs149951572	chr3:121261082-121261083	Strong transcription Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs144166929	chr3:121261087-121261088	Strong transcription Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs116860706	chr3:121261091-121261092	Strong transcription Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs148498353	chr3:121261114-121261115	Strong transcription Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs566185076	chr3:121261156-121261157	Strong transcription Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs144206333	chr3:121261183-121261184	Strong transcription Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs540034965	chr3:121261203-121261204	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs542340877	chr3:121261221-121261222	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs562028584	chr3:121261228-121261229	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs527729531	chr3:121261242-121261243	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs76253777	chr3:121261295-121261296	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs574749860	chr3:121261327-121261328	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs564430210	chr3:121261361-121261362	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs73857910	chr3:121261414-121261415	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:64)

Disease	PMID	Source
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Glioblastoma multiforme	21080181	CNVD
Retinoblastoma	21504564	CNVD
Medulloblastoma	21979893	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	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
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
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	16608533	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Developmental delay	22180640	CNVD
Multiple myeloma	17550852	CNVD
Basal cell lymphoma	21115979	CNVD
Ovarian cancer	22174824	CNVD
lymphocytic leukemia	21291569	CNVD
small cell lung cancer	20016488	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Autism	22241247	CNVD
Pancreatic cancer	17952125	CNVD
Bipolar disorder	17953491	CNVD
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:633 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:121151200-121263800	Weak transcription	Duodenum Mucosa	Duodenum
2	chr3:121178200-121263800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
3	chr3:121200600-121264000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
4	chr3:121202400-121263200	Weak transcription	NHLF	lung
5	chr3:121202400-121263800	Weak transcription	HSMM	muscle
6	chr3:121209400-121263600	Weak transcription	NHDF-Ad	bronchial
7	chr3:121229600-121263000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
8	chr3:121232200-121263800	Weak transcription	Fetal Heart	heart
9	chr3:121233400-121263000	Strong transcription	Primary hematopoietic stem cells short term culture	blood
10	chr3:121234000-121264000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
11	chr3:121234200-121263600	Weak transcription	Osteobl	bone
12	chr3:121234200-121264000	Weak transcription	Fetal Intestine Large	intestine
13	chr3:121234400-121263200	Strong transcription	HUES64 Cell Line	embryonic stem cell
14	chr3:121234600-121263600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
15	chr3:121235000-121263800	Weak transcription	Primary B cells from cord blood	blood
16	chr3:121235000-121264000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
17	chr3:121235400-121263600	Weak transcription	Brain Germinal Matrix	brain
18	chr3:121235600-121262600	Strong transcription	HUES48 Cell Line	embryonic stem cell
19	chr3:121235600-121263600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
20	chr3:121235600-121263600	Weak transcription	NH-A	brain
21	chr3:121235800-121263400	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
22	chr3:121236000-121262600	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
23	chr3:121236600-121263400	Weak transcription	Fetal Intestine Small	intestine
24	chr3:121236600-121264000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
25	chr3:121236600-121264200	Weak transcription	Sigmoid Colon	Sigmoid Colon
26	chr3:121237400-121264000	Weak transcription	Fetal Muscle Trunk	muscle
27	chr3:121237600-121263600	Weak transcription	Muscle Satellite Cultured Cells	--
28	chr3:121237600-121264000	Weak transcription	Fetal Lung	lung
29	chr3:121239200-121263200	Weak transcription	NHEK	skin
30	chr3:121239600-121264000	Weak transcription	Fetal Stomach	stomach
31	chr3:121241800-121263600	Weak transcription	Fetal Muscle Leg	muscle
32	chr3:121243000-121262800	Strong transcription	iPS-18 Cell Line	embryonic stem cell
33	chr3:121243000-121263000	Strong transcription	HUES6 Cell Line	embryonic stem cell
34	chr3:121244200-121262800	Strong transcription	Fetal Thymus	thymus
35	chr3:121244200-121263400	Strong transcription	iPS-20b Cell Line	embryonic stem cell
36	chr3:121246400-121261000	Weak transcription	Rectal Mucosa Donor 31	rectum
37	chr3:121247800-121261800	Strong transcription	Monocytes-CD14+_RO01746	blood
38	chr3:121250000-121264000	Weak transcription	Thymus	Thymus
39	chr3:121251600-121263800	Weak transcription	Fetal Kidney	kidney
40	chr3:121252000-121264000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
41	chr3:121253800-121262600	Strong transcription	A549	lung
42	chr3:121254600-121264200	Weak transcription	Fetal Brain Male	brain
43	chr3:121254800-121263600	Weak transcription	HepG2	liver
44	chr3:121255400-121263200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
45	chr3:121256400-121263600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
46	chr3:121257400-121263600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
47	chr3:121258000-121263000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
48	chr3:121258200-121263600	Weak transcription	HUVEC	blood vessel
49	chr3:121258200-121263800	Weak transcription	H9 Cell Line	embryonic stem cell
50	chr3:121258400-121261000	Weak transcription	Primary neutrophils fromperipheralblood	blood

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