Variant report

Variant	nsv873419
Chromosome Location	chr1:246641827-246664479
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	chr1:246660581-246660971	HepG2	liver:	n/a	n/a
2	ARID3A	chr1:246660564-246660991	K562	blood:	n/a	n/a
3	BATF	chr1:246647202-246648395	GM12878	blood:	n/a	n/a
4	BATF	chr1:246648136-246648477	GM12878	blood:	n/a	n/a
5	BCL11A	chr1:246647613-246648442	GM12878	blood:	n/a	n/a
6	BCLAF1	chr1:246660540-246660998	GM12878	blood:	n/a	n/a
7	BHLHE40	chr1:246660694-246660769	K562	blood:	n/a	n/a
8	CTCF	chr1:246660655-246660916	A549	lung:	n/a	chr1:246660793-246660809 chr1:246660792-246660810 chr1:246660795-246660808 chr1:246660795-246660804
9	CTCF	chr1:246656060-246656210	GM12874	blood:	n/a	chr1:246656117-246656135 chr1:246656119-246656132 chr1:246656112-246656133
10	CTCF	chr1:246656013-246656269	Spleen_OC	spleen:	n/a	chr1:246656117-246656135 chr1:246656119-246656132 chr1:246656112-246656133
11	CTCF	chr1:246660690-246660885	GM13976	blood:	n/a	chr1:246660793-246660809 chr1:246660792-246660810 chr1:246660795-246660808 chr1:246660795-246660804
12	CTCF	chr1:246655857-246656293	T-47D	breast:	n/a	chr1:246656117-246656135 chr1:246656119-246656132 chr1:246656112-246656133
13	CTCF	chr1:246660360-246660510	AG04450	lung:	n/a	n/a
14	CTCF	chr1:246660720-246660870	HBMEC	blood vessel:	n/a	chr1:246660793-246660809 chr1:246660792-246660810 chr1:246660795-246660808 chr1:246660795-246660804
15	CTCF	chr1:246656060-246656210	GM12866	blood:	n/a	chr1:246656117-246656135 chr1:246656119-246656132 chr1:246656112-246656133
16	CTCF	chr1:246656380-246656530	HUVEC	blood vessel:	n/a	n/a
17	CTCF	chr1:246660720-246660870	AG04449	skin:	n/a	chr1:246660793-246660809 chr1:246660792-246660810 chr1:246660795-246660808 chr1:246660795-246660804
18	CTCF	chr1:246656080-246656230	GM12865	blood:	n/a	chr1:246656117-246656135 chr1:246656119-246656132 chr1:246656112-246656133
19	CTCF	chr1:246655933-246656226	H1-hESC	embryonic stem cell:	n/a	chr1:246656117-246656135 chr1:246656119-246656132 chr1:246656112-246656133
20	CTCF	chr1:246656008-246656257	NHEK	skin:	n/a	chr1:246656117-246656135 chr1:246656119-246656132 chr1:246656112-246656133
21	CTCF	chr1:246660685-246660912	Hela-S3	cervix:	n/a	chr1:246660793-246660809 chr1:246660792-246660810 chr1:246660795-246660808 chr1:246660795-246660804
22	CTCF	chr1:246655994-246656237	GM12878	blood:	n/a	chr1:246656117-246656135 chr1:246656119-246656132 chr1:246656112-246656133
23	CTCF	chr1:246660655-246660930	K562	blood:	n/a	chr1:246660793-246660809 chr1:246660792-246660810 chr1:246660795-246660808 chr1:246660795-246660804
24	CTCF	chr1:246656100-246656250	GM12869	blood:	n/a	chr1:246656117-246656135 chr1:246656119-246656132 chr1:246656112-246656133
25	CTCF	chr1:246660740-246660890	HRPEpiC	eye:	n/a	chr1:246660793-246660809 chr1:246660792-246660810 chr1:246660795-246660808 chr1:246660795-246660804
26	CTCF	chr1:246660740-246660890	HPF	lung:	n/a	chr1:246660793-246660809 chr1:246660792-246660810 chr1:246660795-246660808 chr1:246660795-246660804
27	CTCF	chr1:246645540-246645690	HCFaa	heart:	n/a	n/a
28	CTCF	chr1:246656080-246656230	HVMF	connective:	n/a	chr1:246656117-246656135 chr1:246656119-246656132 chr1:246656112-246656133
29	CTCF	chr1:246656080-246656230	WERI-Rb-1	eye:	n/a	chr1:246656117-246656135 chr1:246656119-246656132 chr1:246656112-246656133
30	CTCF	chr1:246656720-246656870	HPAF	blood vessel:	n/a	n/a
31	CTCF	chr1:246660680-246660830	A549	lung:	n/a	chr1:246660793-246660809 chr1:246660792-246660810 chr1:246660795-246660808 chr1:246660795-246660804
32	CTCF	chr1:246645480-246645630	GM12873	blood:	n/a	n/a
33	CTCF	chr1:246655920-246656244	ECC-1	luminal epithelium:	n/a	chr1:246656117-246656135 chr1:246656119-246656132 chr1:246656112-246656133
34	CTCF	chr1:246656100-246656250	BE2_C	brain:	n/a	chr1:246656117-246656135 chr1:246656119-246656132 chr1:246656112-246656133
35	CTCF	chr1:246655808-246656455	HCT-116	colon:	n/a	chr1:246656117-246656135 chr1:246656119-246656132 chr1:246656112-246656133
36	CTCF	chr1:246656060-246656210	HMF	breast:	n/a	chr1:246656117-246656135 chr1:246656119-246656132 chr1:246656112-246656133
37	CTCF	chr1:246661000-246661150	HBMEC	blood vessel:	n/a	n/a
38	CTCF	chr1:246656060-246656210	HRPEpiC	eye:	n/a	chr1:246656117-246656135 chr1:246656119-246656132 chr1:246656112-246656133
39	CTCF	chr1:246660760-246660910	HCM	heart:	n/a	chr1:246660793-246660809 chr1:246660792-246660810 chr1:246660795-246660808 chr1:246660795-246660804
40	CTCF	chr1:246660720-246660870	WERI-Rb-1	eye:	n/a	chr1:246660793-246660809 chr1:246660792-246660810 chr1:246660795-246660808 chr1:246660795-246660804
41	CTCF	chr1:246645780-246645930	GM12864	blood:	n/a	n/a
42	CTCF	chr1:246655977-246656278	K562	blood:	n/a	chr1:246656117-246656135 chr1:246656119-246656132 chr1:246656112-246656133
43	CTCF	chr1:246656040-246656190	HPF	lung:	n/a	chr1:246656117-246656135 chr1:246656119-246656132 chr1:246656112-246656133
44	CTCF	chr1:246656008-246656255	ProgFib	skin:	n/a	chr1:246656117-246656135 chr1:246656119-246656132 chr1:246656112-246656133
45	CTCF	chr1:246656080-246656230	GM12871	blood:	n/a	chr1:246656117-246656135 chr1:246656119-246656132 chr1:246656112-246656133
46	CTCF	chr1:246660740-246660890	GM12871	blood:	n/a	chr1:246660793-246660809 chr1:246660792-246660810 chr1:246660795-246660808 chr1:246660795-246660804
47	CTCF	chr1:246656040-246656190	AG04450	lung:	n/a	chr1:246656117-246656135 chr1:246656119-246656132 chr1:246656112-246656133
48	CTCF	chr1:246645700-246645850	GM12870	blood:	n/a	n/a
49	CTCF	chr1:246660720-246660870	HMF	breast:	n/a	chr1:246660793-246660809 chr1:246660792-246660810 chr1:246660795-246660808 chr1:246660795-246660804
50	CTCF	chr1:246656002-246656247	LNCaP	prostate:	n/a	chr1:246656117-246656135 chr1:246656119-246656132 chr1:246656112-246656133

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:246646424-246646474	AG10803	skin:	n/a
2	chr1:246664003-246664053	AG09319	gingival:	n/a
3	chr1:246646424-246646474	BJ	skin:	n/a
4	chr1:246664003-246664053	MCF-7	breast:	n/a
5	chr1:246646424-246646474	GM12878	blood:	n/a
6	chr1:246646424-246646474	AG04450	lung:	fetal
7	chr1:246664003-246664053	AG09309	skin:	n/a
8	chr1:246664003-246664053	NT2-D1	testis:	n/a
9	chr1:246646424-246646474	SK-N-SH	brain:	n/a
10	chr1:246664003-246664053	HRE	kidney:	n/a
11	chr1:246664003-246664053	HCM	heart:	n/a
12	chr1:246664003-246664053	ECC-1	luminal epithelium:	n/a
13	chr1:246664003-246664053	NH-A	brain:	n/a
14	chr1:246664003-246664053	IMR90	lung:	fetal
15	chr1:246664003-246664053	SK-N-SH_RA	brain:	n/a
16	chr1:246646424-246646474	NHDF-neo	bronchial:	n/a
17	chr1:246646424-246646474	SK-N-MC	brain:	n/a
18	chr1:246664003-246664053	HL-60	blood:	n/a
19	chr1:246646424-246646474	AG04449	skin:	fetal
20	chr1:246646424-246646474	HIPEpiC	eye:	n/a
21	chr1:246646424-246646474	Hela-S3	cervix:	n/a
22	chr1:246646424-246646474	HCF	heart:	n/a
23	chr1:246664003-246664053	A549	lung:	n/a
24	chr1:246646424-246646474	GM12892	blood:	n/a
25	chr1:246646424-246646474	NB4	blood:	n/a
26	chr1:246646424-246646474	AoSMC	blood vessel:	n/a
27	chr1:246646424-246646474	ovcar-3	ovarian:	n/a
28	chr1:246664003-246664053	Caco-2	colon:	n/a
29	chr1:246664003-246664053	HIPEpiC	eye:	n/a
30	chr1:246664003-246664053	Jurkat	blood:	n/a
31	chr1:246646424-246646474	NH-A	brain:	n/a
32	chr1:246664003-246664053	GM19239	blood:	n/a
33	chr1:246646424-246646474	Jurkat	blood:	n/a
34	chr1:246646424-246646474	HepG2	liver:	n/a
35	chr1:246664003-246664053	HUVEC	blood vessel:	n/a
36	chr1:246664003-246664053	ovcar-3	ovarian:	n/a
37	chr1:246646424-246646474	SAEC	small airway:	n/a
38	chr1:246646424-246646474	AG09319	gingival:	n/a
39	chr1:246646424-246646474	PrEC	prostate:	n/a
40	chr1:246664003-246664053	HRPEpiC	eye:	n/a
41	chr1:246646424-246646474	H1-hESC	embryonic stem cell:	embryo
42	chr1:246646424-246646474	ECC-1	luminal epithelium:	n/a
43	chr1:246646424-246646474	HCPEpiC	choroid plexus:	n/a
44	chr1:246646424-246646474	AG09309	skin:	n/a
45	chr1:246646424-246646474	U87	brain:	n/a
46	chr1:246664003-246664053	BE2_C	brain:	n/a
47	chr1:246646424-246646474	NT2-D1	testis:	n/a
48	chr1:246664003-246664053	GM06990	blood:	n/a
49	chr1:246646424-246646474	PANC-1	pancreas:	n/a
50	chr1:246664003-246664053	K562	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr1:246660320..246661257-chr1:246916886..246917830,4	K562	blood:
2	chr1:246658777..246661380-chr1:246664894..246666631,2	K562	blood:
3	chr1:246643346..246644875-chr1:246651223..246652948,2	K562	blood:
4	chr1:246660548..246661305-chr1:246859828..246860357,2	K562	blood:
5	chr1:246664090..246667600-chr1:246667950..246670801,5	K562	blood:
6	chr1:246660152..246661220-chr1:246692463..246693268,3	MCF-7	breast:
7	chr1:246660387..246663593-chr1:246664027..246666681,4	MCF-7	breast:
8	chr1:246660387..246663593-chr1:246664027..246666681,4	MCF-7	breast:
9	chr1:246660382..246660965-chr1:246695565..246696089,2	MCF-7	breast:
10	chr1:246175654..246176170-chr1:246655570..246656125,2	K562	blood:
11	chr1:246635326..246636965-chr1:246661670..246663284,2	K562	blood:
12	chr1:245319905..245320442-chr1:246655652..246656156,2	K562	blood:
13	chr1:246660290..246661312-chr1:246861799..246863185,8	K562	blood:
14	chr1:246662131..246665867-chr1:246667354..246670519,3	K562	blood:
15	chr1:246661655..246664160-chr1:246664640..246667505,3	K562	blood:
16	chr1:246643346..246644875-chr1:246651223..246652948,2	K562	blood:
17	chr1:246660669..246662784-chr1:246700415..246702206,2	MCF-7	breast:

Variant related genes	Relation type
SMYD3	TF binding region
SMYD3	CpG island
ENSG00000185420	chromatin interactions

Extended variants
information (count: 1072 )
Associated
traits (count: 85 )

Variant overlapped rSNPs/rCNVs (count:1072 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs34993482	chr1:246641827-246641828	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs12732613	chr1:246641830-246641831	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs71533480	chr1:246641857-246641858	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs56013798	chr1:246641860-246641861	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs12037546	chr1:246641874-246641875	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs113593839	chr1:246641877-246641878	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs12732937	chr1:246641891-246641892	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs12732938	chr1:246641895-246641896	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs4654265	chr1:246641904-246641905	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs55789719	chr1:246641921-246641922	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs4654267	chr1:246641938-246641939	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs4654268	chr1:246641942-246641943	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs56280002	chr1:246641951-246641952	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs66746206	chr1:246641954-246641955	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs74155517	chr1:246641963-246641964	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs55798324	chr1:246641968-246641969	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs112502695	chr1:246641971-246641972	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs374228850	chr1:246641982-246641983	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs12090818	chr1:246641985-246641986	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs56168934	chr1:246641989-246641990	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs557166483	chr1:246641993-246641994	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs113285829	chr1:246642001-246642002	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs573769879	chr1:246642014-246642015	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs368912888	chr1:246642015-246642016	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs113097940	chr1:246642025-246642026	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs199795801	chr1:246642045-246642046	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs55678047	chr1:246642046-246642047	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs371046092	chr1:246642048-246642049	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs113942001	chr1:246642060-246642061	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs12070644	chr1:246642061-246642062	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs78758484	chr1:246642071-246642072	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs4654269	chr1:246642078-246642079	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs12070648	chr1:246642092-246642093	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs12733258	chr1:246642094-246642095	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs56359709	chr1:246642108-246642109	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs28440833	chr1:246642118-246642119	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs542777918	chr1:246642122-246642123	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs12090857	chr1:246642125-246642126	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs559369019	chr1:246642134-246642135	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs55798322	chr1:246642141-246642142	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs4654266	chr1:246642155-246642156	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs12733274	chr1:246642165-246642166	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs572893336	chr1:246642174-246642175	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs541670772	chr1:246642179-246642180	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs113118634	chr1:246642188-246642189	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs564629255	chr1:246642192-246642193	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs60387604	chr1:246642202-246642203	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs12070678	chr1:246642212-246642213	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs12075932	chr1:246642219-246642220	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs34012138	chr1:246642232-246642233	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:85)

Disease	PMID	Source
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Melanoma	18172304	CNVD
Rett syndrome	21593744	CNVD
Medulloblastoma	21979893	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	CNVD
Non-small cell lung cancer	21044232	CNVD
Cervical cancer	21063398	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	20632083	CNVD
Endometrial cancer	22040021	CNVD
Ewing''s sarcoma	21437220	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	21080181	CNVD
Hepatocellular carcinoma	22174799	CNVD
Medulloblastoma	21292688	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	21264507	CNVD
Liposarcoma	21253554	CNVD
Multiple myeloma	21628407	CNVD
Cancer	16751803	CNVD
Prostate cancer	16705090	CNVD
Neuroblastoma	19435921	CNVD
Breast cancer	17850661	CNVD
Breast cancer	16461572	CNVD
Intracranial tumor	16823260	CNVD
Medulloblastoma	18056178	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Colorectal cancer	16272173	CNVD
Neuroblastoma	21899760	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	16608533	CNVD
Ewing''s sarcoma	22429812	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17001317	CNVD
Acute myeloid leukemia	20729466	CNVD
Testicular germ cell tumor	18059402	CNVD
Neuroblastoma	18923191	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Breast cancer	21509527	CNVD
Urothelial carcinoma	21177765	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Hepatocellular carcinoma	18803288	CNVD
Urothelial tumor	18831757	CNVD
Lung cancer	18438408	CNVD
Medulloblastoma	16783165	CNVD
Basal cell lymphoma	17170743	CNVD
Basal cell lymphoma	17053054	CNVD
Congenital abnormalities	21549014	CNVD
Developmental delay	21549014	CNVD
Mental retardation	21549014	CNVD
small cell lung cancer	20016488	CNVD
Cancer	20164920	CNVD
Cancer	17060936	CNVD
abnormal development	18461090	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Non-small cell lung cancer	21829676	CNVD
Multiple myeloma	16616336	CNVD
Ovarian cancer	21720365	CNVD
Glioblastoma multiforme	22291905	CNVD
Myelofibrosis	22110671	CNVD
Disease	21936942	CNVD
laryngomalacia	21936942	CNVD
GLUT3 deficiency syndrome	20509907	CNVD
Developmental delay	21373258	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Developmental delay	19490664	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Cutaneous malignant melanoma	18794153	CNVD
Astrocytoma	17934521	CNVD
Neurocytoma	17123091	CNVD
Central neurocytomas	17123091	CNVD
Breast cancer	20409316	CNVD
Fibroblasts	17951408	CNVD
Lung cancer	17951408	CNVD
Schizophrenia	20967226	CNVD
Bipolar disorder	19114987	CNVD
Schizophrenia	19805367	CNVD

Chromatin state (count:239 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:246621600-246646400	Weak transcription	Primary B cells from cord blood	blood
2	chr1:246623200-246646600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
3	chr1:246623600-246663200	Weak transcription	Primary T cells from cord blood	blood
4	chr1:246632400-246647000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
5	chr1:246638600-246644200	Weak transcription	Psoas Muscle	Psoas
6	chr1:246640000-246642200	Weak transcription	Skeletal Muscle Male	skeletal muscle
7	chr1:246640400-246646200	Weak transcription	Primary T helper cells PMA-I stimulated	--
8	chr1:246640800-246646200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
9	chr1:246641000-246645800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
10	chr1:246641000-246646000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
11	chr1:246641200-246646200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
12	chr1:246641400-246645600	Weak transcription	GM12878-XiMat	blood
13	chr1:246641400-246646000	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
14	chr1:246641400-246646800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
15	chr1:246641600-246642600	Enhancers	Skeletal Muscle Female	skeletal muscle
16	chr1:246642200-246642600	Enhancers	Skeletal Muscle Male	skeletal muscle
17	chr1:246642400-246642800	Enhancers	Fetal Heart	heart
18	chr1:246642400-246645400	Weak transcription	Small Intestine	intestine
19	chr1:246643400-246643600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
20	chr1:246643600-246644200	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
21	chr1:246644200-246644400	Enhancers	Psoas Muscle	Psoas
22	chr1:246644200-246646200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
23	chr1:246644600-246644800	Enhancers	Primary T helper cells fromperipheralblood	blood
24	chr1:246644800-246648400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
25	chr1:246645400-246646200	Enhancers	Small Intestine	intestine
26	chr1:246645600-246646000	Enhancers	GM12878-XiMat	blood
27	chr1:246645600-246646400	Enhancers	Esophagus	oesophagus
28	chr1:246645600-246647200	Enhancers	Primary B cells from peripheral blood	blood
29	chr1:246645800-246646200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
30	chr1:246645800-246646200	Enhancers	Ovary	ovary
31	chr1:246645800-246646400	Enhancers	Colon Smooth Muscle	Colon
32	chr1:246645800-246646400	Enhancers	Pancreas	Pancrea
33	chr1:246645800-246646400	Enhancers	NHLF	lung
34	chr1:246645800-246646800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
35	chr1:246645800-246647200	Enhancers	Fetal Stomach	stomach
36	chr1:246646000-246646200	Enhancers	NHDF-Ad	bronchial
37	chr1:246646000-246646400	Enhancers	Primary T regulatory cells fromperipheralblood	blood
38	chr1:246646000-246646600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
39	chr1:246646000-246646600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
40	chr1:246646000-246646600	Enhancers	Muscle Satellite Cultured Cells	--
41	chr1:246646000-246647000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
42	chr1:246646000-246647200	Flanking Active TSS	GM12878-XiMat	blood
43	chr1:246646200-246646400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
44	chr1:246646200-246646400	Weak transcription	Primary T helper cells fromperipheralblood	blood
45	chr1:246646200-246646400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
46	chr1:246646200-246646400	Flanking Active TSS	Ovary	ovary
47	chr1:246646200-246646400	Flanking Active TSS	Rectal Smooth Muscle	rectum
48	chr1:246646200-246646400	Enhancers	HSMM	muscle
49	chr1:246646200-246646400	Enhancers	Osteobl	bone
50	chr1:246646200-246646600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--

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