Variant report

Variant	nsv4376
Chromosome Location	chr1:210627620-210672326
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:233)
CpG islands
(count:61)
Chromatin interactive
region (count:28)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:233 , 50 per page) page: 1 2 3 4 5

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr1:210637932-210638494	GM12878	blood:	n/a	n/a
2	ATF2	chr1:210638012-210638455	GM12878	blood:	n/a	n/a
3	ATF3	chr1:210640999-210641267	K562	blood:	n/a	n/a
4	BATF	chr1:210639136-210639554	GM12878	blood:	n/a	n/a
5	BATF	chr1:210638021-210638299	GM12878	blood:	n/a	n/a
6	BATF	chr1:210637954-210638366	GM12878	blood:	n/a	n/a
7	BCL11A	chr1:210638025-210638385	GM12878	blood:	n/a	n/a
8	BCL11A	chr1:210638039-210638323	GM12878	blood:	n/a	n/a
9	BCL3	chr1:210639350-210639648	GM12878	blood:	n/a	n/a
10	BHLHE40	chr1:210638064-210638354	GM12878	blood:	n/a	n/a
11	CEBPB	chr1:210628994-210629199	HepG2	liver:	n/a	n/a
12	CEBPB	chr1:210641060-210641328	H1-hESC	embryonic stem cell:	n/a	chr1:210641180-210641191
13	CEBPB	chr1:210641021-210641339	Hela-S3	cervix:	n/a	chr1:210641180-210641191
14	CEBPB	chr1:210638028-210638458	GM12878	blood:	n/a	n/a
15	CEBPB	chr1:210641013-210641346	IMR90	lung:	n/a	chr1:210641180-210641191
16	CEBPB	chr1:210637985-210638262	IMR90	lung:	n/a	n/a
17	CEBPB	chr1:210641001-210641309	K562	blood:	n/a	chr1:210641180-210641191
18	CEBPB	chr1:210641021-210641359	K562	blood:	n/a	chr1:210641180-210641191
19	CEBPB	chr1:210656624-210656964	H1-hESC	embryonic stem cell:	n/a	n/a
20	CEBPB	chr1:210629023-210629209	A549	lung:	n/a	n/a
21	CEBPB	chr1:210637901-210638298	MCF-7	breast:	n/a	n/a
22	CEBPB	chr1:210669463-210669704	IMR90	lung:	n/a	n/a
23	CEBPB	chr1:210641013-210641368	HepG2	liver:	n/a	chr1:210641180-210641191
24	CEBPB	chr1:210641116-210641283	K562	blood:	n/a	chr1:210641180-210641191
25	CEBPB	chr1:210641012-210641352	A549	lung:	n/a	chr1:210641180-210641191
26	CHD2	chr1:210650762-210650764	Hela-S3	cervix:	n/a	n/a
27	CTCF	chr1:210650900-210651050	NHEK	skin:	n/a	n/a
28	CTCF	chr1:210651040-210651190	HMEC	breast:	n/a	chr1:210651053-210651071
29	CTCF	chr1:210651020-210651170	HCT-116	colon:	n/a	chr1:210651053-210651071
30	CTCF	chr1:210651083-210651094	GM19238	blood:	n/a	n/a
31	CTCF	chr1:210651021-210651134	MCF-7	breast:	n/a	chr1:210651053-210651071
32	CTCF	chr1:210650980-210651130	MCF-7	breast:	n/a	chr1:210651053-210651071
33	CTCF	chr1:210651040-210651190	GM12871	blood:	n/a	chr1:210651053-210651071
34	CTCF	chr1:210650981-210651056	LNCaP	prostate:	n/a	n/a
35	CTCF	chr1:210669560-210669710	BJ	skin:	n/a	n/a
36	CTCF	chr1:210662940-210663090	GM06990	blood:	n/a	n/a
37	CTCF	chr1:210651016-210651139	MCF-7	breast:	n/a	chr1:210651053-210651071
38	CTCF	chr1:210650980-210651130	HEK293	kidney:	n/a	chr1:210651053-210651071
39	CTCF	chr1:210662160-210662215	GM10248	blood:	n/a	n/a
40	CTCF	chr1:210651020-210651170	Hela-S3	cervix:	n/a	chr1:210651053-210651071
41	CTCF	chr1:210650960-210651110	HEK293	kidney:	n/a	chr1:210651053-210651071
42	CTCF	chr1:210651063-210651098	Gliobla	brain:	n/a	n/a
43	CTCF	chr1:210629180-210629330	A549	lung:	n/a	n/a
44	CTCF	chr1:210669480-210669630	HA-sp	spinal cord:	n/a	n/a
45	CTCF	chr1:210650960-210651110	WERI-Rb-1	eye:	n/a	chr1:210651053-210651071
46	CTCF	chr1:210650995-210651130	K562	blood:	n/a	chr1:210651053-210651071
47	CTCF	chr1:210650920-210651070	NB4	blood:	n/a	n/a
48	CTCF	chr1:210651000-210651150	HEEpiC	esophagus:	n/a	chr1:210651053-210651071
49	CTCF	chr1:210651020-210651170	NHEK	skin:	n/a	chr1:210651053-210651071
50	CTCF	chr1:210651004-210651120	GM12878	blood:	n/a	chr1:210651053-210651071

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:210655903-210655953	AG04449	skin:	fetal
2	chr1:210655903-210655953	MCF10A-Er-Src	breast:	n/a
3	chr1:210655903-210655953	K562	blood:	n/a
4	chr1:210655903-210655953	HEK293	kidney:	embryo
5	chr1:210655903-210655953	T-47D	breast:	n/a
6	chr1:210655903-210655953	Hela-S3	cervix:	n/a
7	chr1:210655903-210655953	HCF	heart:	n/a
8	chr1:210655903-210655953	HL-60	blood:	n/a
9	chr1:210655903-210655953	H1-hESC	embryonic stem cell:	embryo
10	chr1:210655903-210655953	GM12891	blood:	n/a
11	chr1:210655903-210655953	PFSK-1	brain:	n/a
12	chr1:210655903-210655953	Caco-2	colon:	n/a
13	chr1:210655903-210655953	HCT-116	colon:	n/a
14	chr1:210655903-210655953	NB4	blood:	n/a
15	chr1:210655903-210655953	GM06990	blood:	n/a
16	chr1:210655903-210655953	HNPCEpiC	eye:	n/a
17	chr1:210655903-210655953	PANC-1	pancreas:	n/a
18	chr1:210655903-210655953	GM12878	blood:	n/a
19	chr1:210655903-210655953	AG09309	skin:	n/a
20	chr1:210655903-210655953	SAEC	small airway:	n/a
21	chr1:210655903-210655953	ProgFib	skin:	n/a
22	chr1:210655903-210655953	NHDF-neo	bronchial:	n/a
23	chr1:210655903-210655953	SKMC	muscle:	n/a
24	chr1:210655903-210655953	MCF-7	breast:	n/a
25	chr1:210655903-210655953	SK-N-SH	brain:	n/a
26	chr1:210655903-210655953	NH-A	brain:	n/a
27	chr1:210655903-210655953	PrEC	prostate:	n/a
28	chr1:210655903-210655953	SK-N-SH_RA	brain:	n/a
29	chr1:210655903-210655953	HPAEpiC	pulmonary alveolar:	n/a
30	chr1:210655903-210655953	NT2-D1	testis:	n/a
31	chr1:210655903-210655953	HRE	kidney:	n/a
32	chr1:210655903-210655953	HUVEC	blood vessel:	n/a
33	chr1:210655903-210655953	SK-N-MC	brain:	n/a
34	chr1:210655903-210655953	HepG2	liver:	n/a
35	chr1:210655903-210655953	HMEC	breast:	n/a
36	chr1:210655903-210655953	HCM	heart:	n/a
37	chr1:210655903-210655953	AoSMC	blood vessel:	n/a
38	chr1:210655903-210655953	HAEpiC	amniotic membrane:	n/a
39	chr1:210655903-210655953	CMK	blood:	n/a
40	chr1:210655903-210655953	HIPEpiC	eye:	n/a
41	chr1:210655903-210655953	RPTEC	kidney:	n/a
42	chr1:210655903-210655953	NHBE	bronchial:	n/a
43	chr1:210655903-210655953	GM19239	blood:	n/a
44	chr1:210655903-210655953	HRPEpiC	eye:	n/a
45	chr1:210655903-210655953	ECC-1	luminal epithelium:	n/a
46	chr1:210655903-210655953	U87	brain:	n/a
47	chr1:210655903-210655953	AG04450	lung:	fetal
48	chr1:210655903-210655953	HCPEpiC	choroid plexus:	n/a
49	chr1:210655903-210655953	BJ	skin:	n/a
50	chr1:210655903-210655953	ovcar-3	ovarian:	n/a

(count:28 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:210636990..210639038-chr1:210644516..210646058,2	MCF-7	breast:
2	chr1:210636990..210639038-chr1:210644516..210646058,2	MCF-7	breast:
3	chr1:210628672..210630917-chr1:211075753..211078223,2	K562	blood:
4	chr1:210546287..210548272-chr1:210649141..210652071,2	MCF-7	breast:
5	chr1:210636675..210638249-chr1:210647138..210649420,2	MCF-7	breast:
6	chr1:210641852..210643783-chr1:210644276..210647020,2	K562	blood:
7	chr1:210636675..210638249-chr1:210647138..210649420,2	MCF-7	breast:
8	chr1:210650763..210653527-chr1:210655583..210657654,2	MCF-7	breast:
9	chr1:210544529..210547501-chr1:210632539..210635313,2	MCF-7	breast:
10	chr1:210632543..210634143-chr1:210644001..210646285,2	K562	blood:
11	chr1:210546346..210549456-chr1:210628612..210630784,3	MCF-7	breast:
12	chr1:210545486..210548370-chr1:210655740..210658368,2	MCF-7	breast:
13	chr1:210650763..210653527-chr1:210655583..210657654,2	MCF-7	breast:
14	chr1:210545901..210548297-chr1:210651689..210655690,4	MCF-7	breast:
15	chr1:210627969..210629666-chr1:211431904..211433827,2	MCF-7	breast:
16	chr1:210645853..210648773-chr1:210649044..210650840,2	MCF-7	breast:
17	chr1:210546164..210547909-chr1:210636773..210638412,2	MCF-7	breast:
18	chr1:210628178..210631075-chr1:210639085..210641802,2	K562	blood:
19	chr1:210544521..210546591-chr1:210638749..210641083,2	MCF-7	breast:
20	chr1:210627850..210630784-chr1:210637225..210638957,2	K562	blood:
21	chr1:210632543..210634143-chr1:210644001..210646285,2	K562	blood:
22	chr1:210641852..210643783-chr1:210644276..210647020,2	K562	blood:
23	chr1:210628178..210631075-chr1:210639085..210641802,2	K562	blood:
24	chr1:210638414..210639957-chr1:210641526..210644422,2	K562	blood:
25	chr1:210645853..210648773-chr1:210649044..210650840,2	MCF-7	breast:
26	chr1:210545478..210547549-chr1:210653820..210655995,2	MCF-7	breast:
27	chr1:210638414..210639957-chr1:210641526..210644422,2	K562	blood:
28	chr1:210627850..210630784-chr1:210637225..210638957,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-KCNH1-6	chr1:210635689-210636356	NONHSAT009267

No data

Variant related genes	Relation type
ENSG00000270936	TF binding region
ENSG00000270936	CpG island
ENSG00000200972	chromatin interactions
ENSG00000117625	chromatin interactions

Extended variants
information (count: 1737 )
Associated
traits (count: 90 )

Variant overlapped rSNPs/rCNVs (count:1737 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs574166423	chr1:210627620-210627621	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs111732010	chr1:210627624-210627625	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs144964459	chr1:210627625-210627626	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs571712590	chr1:210627630-210627631	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs12075789	chr1:210627635-210627636	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs564665693	chr1:210627636-210627637	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs576560979	chr1:210627650-210627651	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs192838881	chr1:210627661-210627662	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs370694418	chr1:210627664-210627665	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs184946067	chr1:210627683-210627684	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs543670755	chr1:210627722-210627723	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs547921587	chr1:210627749-210627750	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs190218191	chr1:210627766-210627767	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs533411447	chr1:210627788-210627789	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs552432040	chr1:210627850-210627851	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs367623822	chr1:210627874-210627875	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs370534894	chr1:210627895-210627896	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs563558361	chr1:210627900-210627901	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs570684657	chr1:210627932-210627933	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs742561	chr1:210628092-210628093	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs58296572	chr1:210628111-210628112	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs181818034	chr1:210628190-210628191	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs60480365	chr1:210628204-210628205	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs138840924	chr1:210628236-210628237	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs553499381	chr1:210628237-210628238	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs186188663	chr1:210628259-210628260	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs571700196	chr1:210628327-210628328	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs189183293	chr1:210628357-210628358	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs558407254	chr1:210628359-210628360	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs61826932	chr1:210628373-210628374	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs148946289	chr1:210628418-210628419	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs3765837	chr1:210628449-210628450	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs181949180	chr1:210628455-210628456	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs541534525	chr1:210628469-210628470	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs533340172	chr1:210628470-210628471	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs184886600	chr1:210628473-210628474	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs547418813	chr1:210628488-210628489	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs567230816	chr1:210628503-210628504	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs563718169	chr1:210628544-210628545	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs116518829	chr1:210628558-210628559	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs143563316	chr1:210628559-210628560	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs368840428	chr1:210628577-210628578	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs189750108	chr1:210628580-210628581	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs529096411	chr1:210628584-210628585	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs148022097	chr1:210628588-210628589	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs141793229	chr1:210628606-210628607	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs539537964	chr1:210628633-210628634	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs368455160	chr1:210628684-210628685	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs557431546	chr1:210628688-210628689	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs183235933	chr1:210628721-210628722	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:90)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Autism	22495311	CNVD
Liposarcoma	21253554	CNVD
Burkitt''s lymphoma	18698080	CNVD
Melanoma	18172304	CNVD
Rett syndrome	21593744	CNVD
Medulloblastoma	21979893	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	17443227	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
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
Acute lymphoblastic leukemia	21098271	CNVD
Neuroblastoma	21899760	CNVD
Glioblastoma multiforme	17002787	CNVD
Breast cancer	21858162	CNVD
Non-small cell lung cancer	21385341	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	16608533	CNVD
Ewing''s sarcoma	22429812	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17001317	CNVD
Acute myeloid leukemia	21251322	CNVD
Multiple myeloma	17550852	CNVD
Prostate cancer	18632612	CNVD
Acute myeloid leukemia	20729466	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Testicular germ cell tumor	18059402	CNVD
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
Neuroblastoma	18923191	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Breast cancer	21509527	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	17393978	CNVD
Hepatocellular carcinoma	16750200	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Trisomy 5 syndrome	21098271	CNVD
Urothelial carcinoma	21177765	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Chordoma	18071362	CNVD
Macular degeneration	22558131	CNVD
Alzheimer''s disease	21403675	CNVD
Multiple myeloma	16461302	CNVD
van der Woude syndrome	22470819	CNVD
van der Woude syndrome	20818247	CNVD
T-cell lymphomas	19863542	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Cancer	17060936	CNVD
Atypical hemolytic uremic syndrome	19861685	CNVD
Hepatocellular carcinoma	18803288	CNVD
Urothelial tumor	18831757	CNVD
Lung cancer	18438408	CNVD
Ovarian cancer	21720365	CNVD
Breast cancer	21364760	CNVD
small cell lung cancer	20016488	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Breast cancer	22522925	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD

Chromatin state (count:210 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:210571400-210641000	Weak transcription	Duodenum Smooth Muscle	Duodenum
2	chr1:210611600-210639600	Weak transcription	Aorta	Aorta
3	chr1:210614600-210641200	Weak transcription	Gastric	stomach
4	chr1:210620200-210637800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
5	chr1:210622000-210630800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
6	chr1:210622400-210631600	Weak transcription	HSMM	muscle
7	chr1:210625800-210638800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
8	chr1:210626200-210650000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
9	chr1:210626400-210628400	Strong transcription	HSMMtube	muscle
10	chr1:210627400-210630800	Weak transcription	Fetal Kidney	kidney
11	chr1:210628000-210629200	Enhancers	Dnd41	blood
12	chr1:210628400-210630600	Genic enhancers	HSMMtube	muscle
13	chr1:210628400-210640800	Weak transcription	Stomach Smooth Muscle	stomach
14	chr1:210629200-210629400	Flanking Active TSS	Dnd41	blood
15	chr1:210629200-210630200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
16	chr1:210629200-210630400	Enhancers	Fetal Thymus	thymus
17	chr1:210629200-210631000	Enhancers	Fetal Muscle Leg	muscle
18	chr1:210629400-210629600	Enhancers	Dnd41	blood
19	chr1:210629400-210630200	Enhancers	Fetal Stomach	stomach
20	chr1:210629600-210629800	Flanking Active TSS	Dnd41	blood
21	chr1:210629800-210630600	Enhancers	Dnd41	blood
22	chr1:210630000-210641200	Weak transcription	Primary hematopoietic stem cells	blood
23	chr1:210630200-210630600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
24	chr1:210630200-210641400	Weak transcription	Liver	Liver
25	chr1:210630600-210631200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
26	chr1:210630600-210634200	Strong transcription	HSMMtube	muscle
27	chr1:210630600-210637800	Weak transcription	Left Ventricle	heart
28	chr1:210630800-210631200	Enhancers	Fetal Kidney	kidney
29	chr1:210630800-210631400	Enhancers	ES-I3 Cell Line	embryonic stem cell
30	chr1:210630800-210631400	Enhancers	ES-WA7 Cell Line	embryonic stem cell
31	chr1:210630800-210631400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
32	chr1:210630800-210631400	Enhancers	iPS-15b Cell Line	embryonic stem cell
33	chr1:210631000-210644200	Weak transcription	Fetal Muscle Leg	muscle
34	chr1:210631000-210653800	Weak transcription	Colon Smooth Muscle	Colon
35	chr1:210631200-210640200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
36	chr1:210631600-210633000	Strong transcription	HSMM	muscle
37	chr1:210632000-210639000	Weak transcription	Lung	lung
38	chr1:210633000-210633200	Enhancers	Brain Inferior Temporal Lobe	brain
39	chr1:210633000-210633400	Enhancers	Brain Substantia Nigra	brain
40	chr1:210633000-210633600	Enhancers	Brain Cingulate Gyrus	brain
41	chr1:210633000-210633800	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
42	chr1:210633000-210638000	Weak transcription	HSMM	muscle
43	chr1:210634200-210637800	Weak transcription	HSMMtube	muscle
44	chr1:210634800-210635000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
45	chr1:210635000-210637800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
46	chr1:210635600-210635800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
47	chr1:210635600-210636400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
48	chr1:210635800-210639800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
49	chr1:210636000-210639400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
50	chr1:210636000-210641000	Weak transcription	Ovary	ovary

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