Variant report

Variant	nsv456429
Chromosome Location	chr2:40823026-40896385
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	CEBPB	chr2:40895614-40895998	Hela-S3	cervix:	n/a	chr2:40895802-40895811 chr2:40895788-40895799 chr2:40895802-40895811 chr2:40895789-40895800 chr2:40895801-40895812 chr2:40895788-40895801 chr2:40895800-40895813 chr2:40895802-40895811
2	CEBPB	chr2:40892639-40893007	Hela-S3	cervix:	n/a	chr2:40892716-40892727 chr2:40892714-40892727 chr2:40892811-40892822 chr2:40892811-40892824
3	CEBPB	chr2:40895669-40895896	HepG2	liver:	n/a	chr2:40895802-40895811 chr2:40895788-40895799 chr2:40895802-40895811 chr2:40895789-40895800 chr2:40895801-40895812 chr2:40895788-40895801 chr2:40895800-40895813 chr2:40895802-40895811
4	CEBPB	chr2:40892756-40892843	K562	blood:	n/a	chr2:40892811-40892822 chr2:40892811-40892824
5	CEBPB	chr2:40864914-40865021	A549	lung:	n/a	chr2:40864924-40864935
6	CEBPB	chr2:40892626-40892989	A549	lung:	n/a	chr2:40892716-40892727 chr2:40892714-40892727 chr2:40892811-40892822 chr2:40892811-40892824
7	CEBPB	chr2:40892679-40892920	IMR90	lung:	n/a	chr2:40892716-40892727 chr2:40892714-40892727 chr2:40892811-40892822 chr2:40892811-40892824
8	CEBPB	chr2:40895618-40895991	IMR90	lung:	n/a	chr2:40895802-40895811 chr2:40895788-40895799 chr2:40895802-40895811 chr2:40895789-40895800 chr2:40895801-40895812 chr2:40895788-40895801 chr2:40895800-40895813 chr2:40895802-40895811
9	CEBPB	chr2:40895622-40895968	K562	blood:	n/a	chr2:40895802-40895811 chr2:40895788-40895799 chr2:40895802-40895811 chr2:40895789-40895800 chr2:40895801-40895812 chr2:40895788-40895801 chr2:40895800-40895813 chr2:40895802-40895811
10	CEBPB	chr2:40895660-40895875	HepG2	liver:	n/a	chr2:40895802-40895811 chr2:40895788-40895799 chr2:40895802-40895811 chr2:40895789-40895800 chr2:40895801-40895812 chr2:40895788-40895801 chr2:40895800-40895813 chr2:40895802-40895811
11	CEBPB	chr2:40895715-40895966	ECC-1	luminal epithelium:	n/a	chr2:40895802-40895811 chr2:40895788-40895799 chr2:40895802-40895811 chr2:40895789-40895800 chr2:40895801-40895812 chr2:40895788-40895801 chr2:40895800-40895813 chr2:40895802-40895811
12	CEBPB	chr2:40895578-40895961	MCF-7	breast:	n/a	chr2:40895802-40895811 chr2:40895788-40895799 chr2:40895802-40895811 chr2:40895789-40895800 chr2:40895801-40895812 chr2:40895788-40895801 chr2:40895800-40895813 chr2:40895802-40895811
13	CEBPB	chr2:40895529-40896063	A549	lung:	n/a	chr2:40895802-40895811 chr2:40895788-40895799 chr2:40895802-40895811 chr2:40895789-40895800 chr2:40895801-40895812 chr2:40895788-40895801 chr2:40895800-40895813 chr2:40895802-40895811
14	CEBPB	chr2:40895610-40895987	A549	lung:	n/a	chr2:40895802-40895811 chr2:40895788-40895799 chr2:40895802-40895811 chr2:40895789-40895800 chr2:40895801-40895812 chr2:40895788-40895801 chr2:40895800-40895813 chr2:40895802-40895811
15	CEBPB	chr2:40853015-40853457	IMR90	lung:	n/a	n/a
16	CEBPB	chr2:40895579-40896016	A549	lung:	n/a	chr2:40895802-40895811 chr2:40895788-40895799 chr2:40895802-40895811 chr2:40895789-40895800 chr2:40895801-40895812 chr2:40895788-40895801 chr2:40895800-40895813 chr2:40895802-40895811
17	CEBPB	chr2:40892690-40892967	MCF-7	breast:	n/a	chr2:40892716-40892727 chr2:40892714-40892727 chr2:40892811-40892822 chr2:40892811-40892824
18	CEBPB	chr2:40892684-40892992	H1-hESC	embryonic stem cell:	n/a	chr2:40892716-40892727 chr2:40892714-40892727 chr2:40892811-40892822 chr2:40892811-40892824
19	CEBPB	chr2:40892625-40893004	HepG2	liver:	n/a	chr2:40892716-40892727 chr2:40892714-40892727 chr2:40892811-40892822 chr2:40892811-40892824
20	CEBPB	chr2:40864774-40865035	IMR90	lung:	n/a	chr2:40864924-40864935
21	CEBPB	chr2:40895615-40895975	H1-hESC	embryonic stem cell:	n/a	chr2:40895802-40895811 chr2:40895788-40895799 chr2:40895802-40895811 chr2:40895789-40895800 chr2:40895801-40895812 chr2:40895788-40895801 chr2:40895800-40895813 chr2:40895802-40895811
22	CEBPB	chr2:40895607-40895988	HepG2	liver:	n/a	chr2:40895802-40895811 chr2:40895788-40895799 chr2:40895802-40895811 chr2:40895789-40895800 chr2:40895801-40895812 chr2:40895788-40895801 chr2:40895800-40895813 chr2:40895802-40895811
23	CEBPB	chr2:40893720-40893812	A549	lung:	n/a	n/a
24	CTCF	chr2:40891217-40891349	MCF-7	breast:	n/a	chr2:40891264-40891282 chr2:40891296-40891304
25	CTCF	chr2:40891240-40891390	BE2_C	brain:	n/a	chr2:40891264-40891282 chr2:40891296-40891304
26	CTCF	chr2:40843055-40843124	Kidney_OC	kidney:	n/a	n/a
27	CTCF	chr2:40869880-40870030	SK-N-SH_RA	brain:	n/a	chr2:40870000-40870021 chr2:40870001-40870010
28	CTCF	chr2:40869840-40869990	BE2_C	brain:	n/a	n/a
29	CTCF	chr2:40891190-40891349	MCF-7	breast:	n/a	chr2:40891264-40891282 chr2:40891296-40891304
30	CTCF	chr2:40835900-40836050	NHEK	skin:	n/a	n/a
31	CTCF	chr2:40869900-40870050	HMF	breast:	n/a	chr2:40870000-40870021 chr2:40870001-40870010
32	CTCF	chr2:40869900-40870050	BE2_C	brain:	n/a	chr2:40870000-40870021 chr2:40870001-40870010
33	CTCF	chr2:40891180-40891330	WERI-Rb-1	eye:	n/a	chr2:40891264-40891282 chr2:40891296-40891304
34	E2F4	chr2:40835780-40835952	MCF10A-Er-Src	breast:	n/a	n/a
35	E2F4	chr2:40881190-40881398	MCF10A-Er-Src	breast:	n/a	n/a
36	EP300	chr2:40894428-40894440	K562	blood:	n/a	n/a
37	EP300	chr2:40888133-40888264	GM12878	blood:	n/a	n/a
38	EP300	chr2:40869459-40869676	SK-N-SH_RA	brain:	n/a	n/a
39	EP300	chr2:40895789-40895858	HepG2	liver:	n/a	n/a
40	EP300	chr2:40853241-40853243	GM12878	blood:	n/a	n/a
41	EP300	chr2:40869404-40869688	SK-N-SH_RA	brain:	n/a	n/a
42	EP300	chr2:40843652-40844316	SK-N-SH	brain:	n/a	n/a
43	FOS	chr2:40852992-40853412	MCF10A-Er-Src	breast:	n/a	chr2:40853169-40853180 chr2:40853215-40853227 chr2:40853217-40853225
44	FOS	chr2:40853013-40853377	MCF10A-Er-Src	breast:	n/a	chr2:40853169-40853180 chr2:40853215-40853227 chr2:40853217-40853225
45	FOS	chr2:40880931-40881442	MCF10A-Er-Src	breast:	n/a	chr2:40881290-40881299
46	FOS	chr2:40895673-40895915	MCF10A-Er-Src	breast:	n/a	chr2:40895786-40895798
47	FOS	chr2:40880970-40881348	MCF10A-Er-Src	breast:	n/a	chr2:40881290-40881299
48	FOS	chr2:40852959-40853404	MCF10A-Er-Src	breast:	n/a	chr2:40853169-40853180 chr2:40853215-40853227 chr2:40853217-40853225
49	FOS	chr2:40853018-40853306	HUVEC	blood vessel:	n/a	chr2:40853169-40853180 chr2:40853215-40853227 chr2:40853217-40853225
50	FOS	chr2:40880941-40881695	MCF10A-Er-Src	breast:	n/a	chr2:40881290-40881299

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:40845989-40846039	AG04449	skin:	fetal
2	chr2:40845989-40846039	SK-N-MC	brain:	n/a
3	chr2:40845989-40846039	Hela-S3	cervix:	n/a
4	chr2:40845989-40846039	ovcar-3	ovarian:	n/a
5	chr2:40845989-40846039	PFSK-1	brain:	n/a
6	chr2:40845989-40846039	AG10803	skin:	n/a
7	chr2:40845989-40846039	CMK	blood:	n/a
8	chr2:40845989-40846039	SKMC	muscle:	n/a
9	chr2:40845989-40846039	AoSMC	blood vessel:	n/a
10	chr2:40845989-40846039	A549	lung:	n/a
11	chr2:40845989-40846039	ProgFib	skin:	n/a
12	chr2:40845989-40846039	PrEC	prostate:	n/a
13	chr2:40845989-40846039	HAEpiC	amniotic membrane:	n/a
14	chr2:40845989-40846039	GM06990	blood:	n/a
15	chr2:40845989-40846039	BE2_C	brain:	n/a
16	chr2:40845989-40846039	AG04450	lung:	fetal
17	chr2:40845989-40846039	U87	brain:	n/a
18	chr2:40845989-40846039	NHDF-neo	bronchial:	n/a
19	chr2:40845989-40846039	HEK293	kidney:	embryo
20	chr2:40845989-40846039	HNPCEpiC	eye:	n/a
21	chr2:40845989-40846039	GM12878	blood:	n/a
22	chr2:40845989-40846039	K562	blood:	n/a
23	chr2:40845989-40846039	HCM	heart:	n/a
24	chr2:40845989-40846039	HCPEpiC	choroid plexus:	n/a
25	chr2:40845989-40846039	IMR90	lung:	fetal
26	chr2:40845989-40846039	BJ	skin:	n/a
27	chr2:40845989-40846039	NB4	blood:	n/a
28	chr2:40845989-40846039	NHBE	bronchial:	n/a
29	chr2:40845989-40846039	HIPEpiC	eye:	n/a
30	chr2:40845989-40846039	NH-A	brain:	n/a
31	chr2:40845989-40846039	AG09309	skin:	n/a
32	chr2:40845989-40846039	PANC-1	pancreas:	n/a
33	chr2:40845989-40846039	Hepatocyte	liver:	n/a
34	chr2:40845989-40846039	LNCaP	prostate:	n/a
35	chr2:40845989-40846039	T-47D	breast:	n/a
36	chr2:40845989-40846039	HCF	heart:	n/a
37	chr2:40845989-40846039	HPAEpiC	pulmonary alveolar:	n/a
38	chr2:40845989-40846039	AG09319	gingival:	n/a
39	chr2:40845989-40846039	SK-N-SH_RA	brain:	n/a
40	chr2:40845989-40846039	HL-60	blood:	n/a
41	chr2:40845989-40846039	GM12892	blood:	n/a
42	chr2:40845989-40846039	Jurkat	blood:	n/a
43	chr2:40845989-40846039	MCF10A-Er-Src	breast:	n/a
44	chr2:40845989-40846039	MCF-7	breast:	n/a
45	chr2:40845989-40846039	HUVEC	blood vessel:	n/a
46	chr2:40845989-40846039	HRCEpiC	kidney:	n/a
47	chr2:40845989-40846039	HRPEpiC	eye:	n/a
48	chr2:40845989-40846039	NT2-D1	testis:	n/a
49	chr2:40845989-40846039	SAEC	small airway:	n/a
50	chr2:40845989-40846039	RPTEC	kidney:	n/a

No.	Distal block	Cell Line	Cell type
1	chr2:40863344..40866000-chr2:40868912..40871639,2	K562	blood:
2	chr2:40868683..40869510-chr2:58548247..58548778,2	MCF-7	breast:
3	chr2:40869635..40872329-chr2:40880298..40882464,2	K562	blood:
4	chr2:40863344..40866000-chr2:40868912..40871639,2	K562	blood:
5	chr2:40869635..40872329-chr2:40880298..40882464,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TMEM178-7	chr2:40835265-40835273	l_1815_chr2:40835264-40838463_testes
2	lnc-TMEM178-7	chr2:40827131-40827296	NONHSAT070282
3	lnc-TMEM178-7	chr2:40835782-40835863	NONHSAT070282
4	lnc-TMEM178-7	chr2:40835210-40835273	NONHSAT070282
5	lnc-TMEM178-7	chr2:40847860-40848096	NONHSAT070282
6	lnc-TMEM178-7	chr2:40838265-40838463	l_1815_chr2:40835264-40838463_testes
7	lnc-TMEM178-7	chr2:40835782-40835863	l_1815_chr2:40835264-40838463_testes

Variant related genes	Relation type
SLC8A1	TF binding region
SLC8A1	CpG island

Extended variants
information (count: 1941 )
Associated
traits (count: 59 )

Variant overlapped rSNPs/rCNVs (count:1941 , 50 per page) page: 1 2 3 4 5 6 7 ... 39

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs42822	chr2:40823026-40823027	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs534536437	chr2:40823034-40823035	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs529851962	chr2:40823044-40823045	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs183840997	chr2:40823051-40823052	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs566553861	chr2:40823062-40823063	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs188683574	chr2:40823082-40823083	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs374206253	chr2:40823115-40823116	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs10182242	chr2:40823148-40823149	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs533360413	chr2:40823151-40823152	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs570079647	chr2:40823157-40823158	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs537468734	chr2:40823189-40823190	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs537413933	chr2:40823197-40823198	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs377194112	chr2:40823215-40823216	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs557185240	chr2:40823320-40823321	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs574236136	chr2:40823331-40823332	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs148546929	chr2:40823332-40823333	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs570959829	chr2:40823335-40823336	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs536841218	chr2:40823355-40823356	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs554908636	chr2:40823356-40823357	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs142613581	chr2:40823362-40823363	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs193286786	chr2:40823385-40823386	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs556199708	chr2:40823391-40823392	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs559112606	chr2:40823403-40823404	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs150973791	chr2:40823405-40823406	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs78565034	chr2:40823420-40823421	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs140511876	chr2:40823433-40823434	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs144485734	chr2:40823444-40823445	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs147854017	chr2:40823470-40823471	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs544975458	chr2:40823478-40823479	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs184972500	chr2:40823499-40823500	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs527370092	chr2:40823507-40823508	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs551827088	chr2:40823528-40823529	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs141104584	chr2:40823566-40823567	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs531168537	chr2:40823572-40823573	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs549551358	chr2:40823598-40823599	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs42821	chr2:40823602-40823603	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs42820	chr2:40823633-40823634	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs555127715	chr2:40823641-40823642	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs150303851	chr2:40823643-40823644	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs572349767	chr2:40823661-40823662	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs536142963	chr2:40823688-40823689	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs542467386	chr2:40823692-40823693	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs560859559	chr2:40823704-40823705	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs534418895	chr2:40823735-40823736	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs554816265	chr2:40823740-40823741	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs77279437	chr2:40823762-40823763	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs371466550	chr2:40823783-40823784	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs186612834	chr2:40823798-40823799	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs544608150	chr2:40823800-40823801	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs556329816	chr2:40823841-40823842	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:59)

Disease	PMID	Source
Breast cancer	17393978	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Breast cancer	17603634	CNVD
Medulloblastoma	21979893	CNVD
Lynch syndrome	18415027	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17387387	CNVD
Neuroblastoma	17533364	CNVD
Neuroblastoma	18923191	CNVD
Endometrial cancer	22040021	CNVD
Adrenal tumor	17535989	CNVD
Breast cancer	21264507	CNVD
Basal cell lymphoma	17053054	CNVD
Medulloblastoma	17522785	CNVD
Cancer	23418310	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Ependymoma	16718352	CNVD
lymphocytic leukemia	21291569	CNVD
Prostate cancer	18632612	CNVD
Bladder cancer	21909424	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Follicular lymphoma	20505157	CNVD
Autism	17483303	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Medulloblastoma	20607354	CNVD
Leukemia	18628472	CNVD
Autism	22495311	CNVD
Autism	19521722	CNVD
Autism	18522746	CNVD
Non-small cell lung cancer	18927303	CNVD
Breast cancer	21785460	CNVD
Lung cancer	18438408	CNVD
Prostate cancer	21965145	CNVD
Breast cancer	16397240	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	21508638	CNVD
Neurodevelopmental disorder	22521361	CNVD
Neurocytoma	17123091	CNVD
small cell lung cancer	20016488	CNVD
Melanoma	18172304	CNVD
Cancer	16751803	CNVD
Breast cancer	21364760	CNVD
Colorectal cancer	16272173	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Williams Syndrome	20824207	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:106 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:40820200-40832600	Weak transcription	Right Atrium	heart
2	chr2:40820400-40823200	Weak transcription	Fetal Heart	heart
3	chr2:40823200-40823800	Enhancers	Fetal Heart	heart
4	chr2:40832600-40832800	Enhancers	Right Atrium	heart
5	chr2:40833600-40834000	Active TSS	Primary T helper memory cells from peripheral blood 1	blood
6	chr2:40833600-40834800	Enhancers	HMEC	breast
7	chr2:40833800-40834200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
8	chr2:40833800-40834200	Enhancers	NH-A	brain
9	chr2:40833800-40834600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
10	chr2:40833800-40834600	Enhancers	Osteobl	bone
11	chr2:40836200-40836600	Enhancers	ES-I3 Cell Line	embryonic stem cell
12	chr2:40843800-40844400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
13	chr2:40844400-40853000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
14	chr2:40852200-40853800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
15	chr2:40852400-40853200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
16	chr2:40852400-40853200	Enhancers	NHDF-Ad	bronchial
17	chr2:40852400-40854000	Enhancers	NHEK	skin
18	chr2:40852600-40853400	Enhancers	Muscle Satellite Cultured Cells	--
19	chr2:40852600-40853400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
20	chr2:40852800-40853600	Enhancers	Osteobl	bone
21	chr2:40853000-40854200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
22	chr2:40856800-40857200	Enhancers	Colon Smooth Muscle	Colon
23	chr2:40864200-40864400	Enhancers	Colon Smooth Muscle	Colon
24	chr2:40864400-40869200	Weak transcription	Colon Smooth Muscle	Colon
25	chr2:40866200-40867000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
26	chr2:40866200-40867400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
27	chr2:40866400-40867000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
28	chr2:40866600-40866800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
29	chr2:40866800-40867000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
30	chr2:40866800-40869000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
31	chr2:40867800-40869400	Enhancers	Primary neutrophils fromperipheralblood	blood
32	chr2:40868600-40869200	Enhancers	HUVEC	blood vessel
33	chr2:40869000-40871400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
34	chr2:40869200-40869600	Enhancers	Rectal Smooth Muscle	rectum
35	chr2:40869200-40870400	Enhancers	Colon Smooth Muscle	Colon
36	chr2:40871400-40875200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
37	chr2:40875200-40877000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
38	chr2:40876000-40876200	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
39	chr2:40876400-40878200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
40	chr2:40877000-40878000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
41	chr2:40878000-40878200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
42	chr2:40878000-40878600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
43	chr2:40878200-40878600	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
44	chr2:40878200-40878600	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
45	chr2:40878600-40879600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
46	chr2:40878600-40879800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
47	chr2:40879800-40880000	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
48	chr2:40879800-40880400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
49	chr2:40880000-40882200	Enhancers	NHEK	skin
50	chr2:40880400-40880800	Enhancers	HMEC	breast

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links