Variant report

Variant	nsv548076
Chromosome Location	chr1:161693003-161702792
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:912)
CpG islands
(count:917)
Chromatin interactive
region (count:23)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:912 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:161697652-161697745	K562	blood:	n/a	n/a
2	ARID3A	chr1:161699977-161700240	K562	blood:	n/a	n/a
3	ATF2	chr1:161699874-161700460	GM12878	blood:	n/a	n/a
4	ATF2	chr1:161697416-161697766	GM12878	blood:	n/a	n/a
5	ATF2	chr1:161697348-161697828	GM12878	blood:	n/a	n/a
6	ATF2	chr1:161696508-161697180	GM12878	blood:	n/a	n/a
7	BACH1	chr1:161697132-161697292	K562	blood:	n/a	n/a
8	BACH1	chr1:161697016-161697610	H1-hESC	embryonic stem cell:	n/a	n/a
9	BACH1	chr1:161695615-161696769	H1-hESC	embryonic stem cell:	n/a	n/a
10	BACH1	chr1:161696097-161696123	K562	blood:	n/a	n/a
11	BATF	chr1:161697444-161697722	GM12878	blood:	n/a	n/a
12	BATF	chr1:161700037-161700334	GM12878	blood:	n/a	chr1:161700245-161700256
13	BATF	chr1:161700015-161700435	GM12878	blood:	n/a	chr1:161700245-161700256
14	BCL11A	chr1:161700027-161700391	GM12878	blood:	n/a	n/a
15	BCL3	chr1:161696620-161697171	GM12878	blood:	n/a	n/a
16	BCLAF1	chr1:161697335-161697827	GM12878	blood:	n/a	n/a
17	BCLAF1	chr1:161695565-161696820	K562	blood:	n/a	n/a
18	BCLAF1	chr1:161695962-161697186	GM12878	blood:	n/a	n/a
19	BCLAF1	chr1:161696353-161696875	GM12878	blood:	n/a	n/a
20	BCLAF1	chr1:161695548-161696333	GM12878	blood:	n/a	n/a
21	BHLHE40	chr1:161696702-161697167	A549	lung:	n/a	n/a
22	BHLHE40	chr1:161695665-161697806	GM12878	blood:	n/a	n/a
23	BHLHE40	chr1:161696883-161697216	HepG2	liver:	n/a	n/a
24	BHLHE40	chr1:161700751-161700770	K562	blood:	n/a	n/a
25	BHLHE40	chr1:161696037-161697726	K562	blood:	n/a	n/a
26	BRCA1	chr1:161696585-161696626	HepG2	liver:	n/a	n/a
27	BRCA1	chr1:161696978-161697508	H1-hESC	embryonic stem cell:	n/a	n/a
28	CBX3	chr1:161695717-161697392	K562	blood:	n/a	n/a
29	CCNT2	chr1:161695674-161697487	K562	blood:	n/a	n/a
30	CEBPB	chr1:161698673-161698968	Hela-S3	cervix:	n/a	n/a
31	CEBPB	chr1:161700053-161700340	IMR90	lung:	n/a	n/a
32	CEBPB	chr1:161695770-161696076	IMR90	lung:	n/a	n/a
33	CEBPB	chr1:161701973-161702147	A549	lung:	n/a	n/a
34	CEBPB	chr1:161700903-161701098	K562	blood:	n/a	n/a
35	CEBPB	chr1:161698621-161698990	K562	blood:	n/a	n/a
36	CEBPB	chr1:161698644-161698967	IMR90	lung:	n/a	n/a
37	CEBPB	chr1:161698657-161698967	A549	lung:	n/a	n/a
38	CEBPB	chr1:161695863-161695924	K562	blood:	n/a	n/a
39	CEBPB	chr1:161698748-161698935	HepG2	liver:	n/a	n/a
40	CEBPB	chr1:161698773-161698833	H1-hESC	embryonic stem cell:	n/a	n/a
41	CEBPB	chr1:161701880-161702176	K562	blood:	n/a	n/a
42	CEBPB	chr1:161701940-161702155	K562	blood:	n/a	n/a
43	CEBPD	chr1:161696537-161696906	K562	blood:	n/a	n/a
44	CHD1	chr1:161696551-161696695	H1-hESC	embryonic stem cell:	n/a	n/a
45	CHD1	chr1:161696188-161697665	GM12878	blood:	n/a	n/a
46	CHD2	chr1:161700176-161700238	Hela-S3	cervix:	n/a	n/a
47	CHD2	chr1:161696820-161697209	HepG2	liver:	n/a	n/a
48	CHD2	chr1:161695909-161697219	K562	blood:	n/a	n/a
49	CHD2	chr1:161696323-161697166	Hela-S3	cervix:	n/a	n/a
50	CHD2	chr1:161695732-161695932	H1-hESC	embryonic stem cell:	n/a	n/a

(count:917 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:161693987-161694037	RPTEC	kidney:	n/a
2	chr1:161695961-161696011	HEK293	kidney:	embryo
3	chr1:161693987-161694037	RPTEC	kidney:	n/a
4	chr1:161695961-161696011	HEK293	kidney:	embryo
5	chr1:161697574-161697624	NB4	blood:	n/a
6	chr1:161695961-161696011	HIPEpiC	eye:	n/a
7	chr1:161696082-161696132	NHBE	bronchial:	n/a
8	chr1:161697052-161697102	HIPEpiC	eye:	n/a
9	chr1:161700167-161700217	ProgFib	skin:	n/a
10	chr1:161696175-161696225	Jurkat	blood:	n/a
11	chr1:161696302-161696352	NHBE	bronchial:	n/a
12	chr1:161693987-161694037	SAEC	small airway:	n/a
13	chr1:161695961-161696011	HNPCEpiC	eye:	n/a
14	chr1:161693088-161693138	NHBE	bronchial:	n/a
15	chr1:161697083-161697133	NH-A	brain:	n/a
16	chr1:161695659-161695709	HRCEpiC	kidney:	n/a
17	chr1:161700167-161700217	LNCaP	prostate:	n/a
18	chr1:161697052-161697102	SKMC	muscle:	n/a
19	chr1:161697241-161697291	SAEC	small airway:	n/a
20	chr1:161696175-161696225	AoSMC	blood vessel:	n/a
21	chr1:161697281-161697331	RPTEC	kidney:	n/a
22	chr1:161696175-161696225	GM19239	blood:	n/a
23	chr1:161693088-161693138	PFSK-1	brain:	n/a
24	chr1:161695961-161696011	RPTEC	kidney:	n/a
25	chr1:161696082-161696132	CMK	blood:	n/a
26	chr1:161695659-161695709	MCF-7	breast:	n/a
27	chr1:161696082-161696132	K562	blood:	n/a
28	chr1:161697574-161697624	AG04450	lung:	fetal
29	chr1:161696302-161696352	HCT-116	colon:	n/a
30	chr1:161697241-161697291	AoSMC	blood vessel:	n/a
31	chr1:161695961-161696011	GM12878	blood:	n/a
32	chr1:161695678-161695728	HCT-116	colon:	n/a
33	chr1:161695659-161695709	GM12892	blood:	n/a
34	chr1:161697241-161697291	NT2-D1	testis:	n/a
35	chr1:161693088-161693138	HUVEC	blood vessel:	n/a
36	chr1:161693987-161694037	SK-N-SH_RA	brain:	n/a
37	chr1:161696302-161696352	ovcar-3	ovarian:	n/a
38	chr1:161697241-161697291	SKMC	muscle:	n/a
39	chr1:161695659-161695709	HUVEC	blood vessel:	n/a
40	chr1:161696302-161696352	A549	lung:	n/a
41	chr1:161697052-161697102	K562	blood:	n/a
42	chr1:161697574-161697624	U87	brain:	n/a
43	chr1:161695678-161695728	HEEpiC	esophagus:	n/a
44	chr1:161693088-161693138	GM12878	blood:	n/a
45	chr1:161700167-161700217	HCM	heart:	n/a
46	chr1:161697052-161697102	PANC-1	pancreas:	n/a
47	chr1:161695839-161695889	HCF	heart:	n/a
48	chr1:161693088-161693138	AG04449	skin:	fetal
49	chr1:161697083-161697133	GM12891	blood:	n/a
50	chr1:161697281-161697331	HIPEpiC	eye:	n/a

(count:23 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:161591405..161593904-chr1:161697560..161699954,2	K562	blood:
2	chr1:161683127..161685809-chr1:161696033..161698160,3	MCF-7	breast:
3	chr1:161694367..161698874-chr1:161718174..161721030,6	MCF-7	breast:
4	chr1:161696482..161699035-chr1:161718061..161722028,6	K562	blood:
5	chr1:161696672..161698764-chr1:161719597..161721628,3	K562	blood:
6	chr1:161474965..161477021-chr1:161694558..161697249,2	K562	blood:
7	chr1:161702286..161705058-chr1:161705873..161710501,6	K562	blood:
8	chr1:161474965..161476524-chr1:161694397..161697249,2	K562	blood:
9	chr1:161696512..161697495-chr11:66610830..66611790,2	NB4	blood:
10	chr1:161696651..161697360-chr16:2961887..2962457,2	NB4	blood:
11	chr1:161695790..161697784-chr8:91655626..91657821,2	MCF-7	breast:
12	chr1:161651291..161653505-chr1:161696476..161699114,3	K562	blood:
13	chr1:161696233..161698594-chr1:161718488..161721013,2	MCF-7	breast:
14	chr1:161640986..161643411-chr1:161696404..161699095,2	MCF-7	breast:
15	chr1:161697451..161700405-chr1:161734526..161737492,2	K562	blood:
16	chr1:161695918..161698329-chr1:161735226..161737077,2	MCF-7	breast:
17	chr1:161696821..161698460-chr1:161718041..161719561,2	K562	blood:
18	chr1:161535342..161537175-chr1:161695826..161698506,2	MCF-7	breast:
19	chr1:161648385..161650314-chr1:161696093..161698220,2	K562	blood:
20	chr1:161645664..161648632-chr1:161696817..161700044,3	K562	blood:
21	chr1:161696699..161697640-chr1:161719530..161720155,2	MCF-7	breast:
22	chr1:161654373..161658306-chr1:161696464..161699587,3	MCF-7	breast:
23	chr1:161657417..161659539-chr1:161696325..161698709,3	K562	blood:

No data

Variant related genes	Relation type
FCRLB	TF binding region
RN7SL466P	TF binding region
FCRLB	CpG island
RN7SL466P	CpG island
ENSG00000143226	chromatin interactions
ENSG00000226889	chromatin interactions
ENSG00000173653	chromatin interactions
ENSG00000081721	chromatin interactions
ENSG00000213075	chromatin interactions
ENSG00000118217	chromatin interactions
ENSG00000180694	chromatin interactions
ENSG00000059122	chromatin interactions

Extended variants
information (count: 420 )
Associated
traits (count: 108 )

Variant overlapped rSNPs/rCNVs (count:420 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4657093	chr1:161693003-161693004	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs565158426	chr1:161693019-161693020	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs573752662	chr1:161693027-161693028	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs183579115	chr1:161693029-161693030	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs544349150	chr1:161693051-161693052	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs561094070	chr1:161693085-161693086	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs530126963	chr1:161693140-161693141	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs546625220	chr1:161693165-161693166	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs375713081	chr1:161693183-161693184	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs267598139	chr1:161693190-161693191	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs200559498	chr1:161693191-161693192	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs35002732	chr1:161693199-161693200	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs141950344	chr1:161693220-161693221	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs571029267	chr1:161693234-161693235	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs188912871	chr1:161693238-161693239	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs541451917	chr1:161693262-161693263	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs139092332	chr1:161693270-161693271	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs139828673	chr1:161693280-161693281	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs367719903	chr1:161693287-161693288	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs146761628	chr1:161693307-161693308	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs371595857	chr1:161693315-161693316	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs376950725	chr1:161693318-161693319	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs139259107	chr1:161693326-161693327	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs538056349	chr1:161693328-161693329	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs150995653	chr1:161693340-161693341	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs201479109	chr1:161693366-161693367	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs567408157	chr1:161693370-161693371	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs544994907	chr1:161693377-161693378	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs147870526	chr1:161693378-161693379	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs553032070	chr1:161693381-161693382	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs369117765	chr1:161693424-161693425	Enhancers Weak transcription Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs572771679	chr1:161693428-161693429	Enhancers Weak transcription Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs538594471	chr1:161693429-161693430	Enhancers Weak transcription Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs373232160	chr1:161693434-161693435	Enhancers Weak transcription Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs558577824	chr1:161693438-161693439	Enhancers Weak transcription Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs575492581	chr1:161693443-161693444	Enhancers Weak transcription Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs544043340	chr1:161693446-161693447	Enhancers Weak transcription Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs368349211	chr1:161693459-161693460	Enhancers Weak transcription Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs560734720	chr1:161693472-161693473	Enhancers Weak transcription Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs574621706	chr1:161693534-161693535	Enhancers Weak transcription Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs564979880	chr1:161693563-161693564	Enhancers Weak transcription Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs530570871	chr1:161693565-161693566	Enhancers Weak transcription Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs111835451	chr1:161693577-161693578	Enhancers Weak transcription Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs552495473	chr1:161693593-161693594	Enhancers Weak transcription Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs67476681	chr1:161693679-161693680	Enhancers Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs532020504	chr1:161693709-161693710	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs530215579	chr1:161693728-161693729	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs548832074	chr1:161693797-161693798	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs12729592	chr1:161693810-161693811	Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs534360562	chr1:161693839-161693840	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:108)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Liposarcoma	21253554	CNVD
Non-small cell lung cancer	21385341	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	18698080	CNVD
Melanoma	18172304	CNVD
Cervical cancer	21062161	CNVD
Glioblastoma multiforme	21080181	CNVD
Cancer	21183584	CNVD
Multiple myeloma	16461302	CNVD
Lung cancer	18438408	CNVD
Rett syndrome	21593744	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Medulloblastoma	21979893	CNVD
Systemic lupus erythematosus	21956041	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	CNVD
Non-small cell lung cancer	21829676	CNVD
Carcinoma ex pleomorphic adenoma	18828159	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
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
Breast cancer	17899364	CNVD
Bladder cancer	19088036	CNVD
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17002787	CNVD
Breast cancer	21858162	CNVD
Retinoblastoma	19183342	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	16608533	CNVD
Ewing''s sarcoma	22429812	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Type 2 diabetes	19141583	CNVD
Chordoma	18071362	CNVD
Hepatocellular carcinoma	18803288	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17001317	CNVD
Urothelial carcinoma	21177765	CNVD
Burkitt''s lymphoma	19759907	CNVD
Acute myeloid leukemia	21251322	CNVD
Multiple myeloma	17550852	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21509527	CNVD
Bladder cancer	21909424	CNVD
Acute myeloid leukemia	20729466	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Testicular germ cell tumor	18059402	CNVD
Trisomy 5 syndrome	21098271	CNVD
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
Breast cancer	21611746	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Neuroblastoma	18923191	CNVD
Systemic lupus erythematosus	19220326	CNVD
Systemic lupus erythematosus	19287148	CNVD
Glomerulonephritis	19341492	CNVD
Systemic lupus erythematosus	18559452	CNVD
Systemic autoimmune disease	17597778	CNVD
Glomerulonephritis	17008540	CNVD
Glomerulonephritis	16482158	CNVD
Soft tissue tumor	16732325	CNVD
Cancer	17060936	CNVD
Lung cancer	16740712	CNVD
Breast cancer	21045282	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Ewing''s sarcoma	17952124	CNVD
Follicular lymphoma	18703704	CNVD
Myelofibrosis	22110671	CNVD
Intracranial ependymoma	16609018	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	20409316	CNVD
Mental retardation	17847001	CNVD
Idiopathic thrombocytopenic purpura	17827395	CNVD
Acute lymphoblastic leukemia	19100363	CNVD

Chromatin state (count:637 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:161689000-161695400	Weak transcription	Primary T helper cells fromperipheralblood	blood
2	chr1:161689000-161695600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
3	chr1:161692200-161693400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
4	chr1:161692200-161694800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
5	chr1:161692200-161695400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
6	chr1:161692200-161695400	Weak transcription	A549	lung
7	chr1:161692200-161695600	Enhancers	K562	blood
8	chr1:161692400-161693400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
9	chr1:161692400-161693600	Weak transcription	NHEK	skin
10	chr1:161692400-161695000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
11	chr1:161692400-161695400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
12	chr1:161692400-161695400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
13	chr1:161692400-161695400	Weak transcription	HUVEC	blood vessel
14	chr1:161692400-161695400	Weak transcription	NH-A	brain
15	chr1:161692400-161695600	Weak transcription	Gastric	stomach
16	chr1:161692600-161693600	Weak transcription	HMEC	breast
17	chr1:161692600-161693800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
18	chr1:161692600-161694600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
19	chr1:161692600-161694600	Weak transcription	Osteobl	bone
20	chr1:161692600-161694800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
21	chr1:161692600-161694800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
22	chr1:161692600-161694800	Weak transcription	GM12878-XiMat	blood
23	chr1:161692600-161695000	Weak transcription	Spleen	Spleen
24	chr1:161692600-161695400	Weak transcription	Muscle Satellite Cultured Cells	--
25	chr1:161692600-161695400	Weak transcription	NHLF	lung
26	chr1:161692600-161695600	Weak transcription	HSMMtube	muscle
27	chr1:161692800-161693200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
28	chr1:161692800-161693800	Weak transcription	NHDF-Ad	bronchial
29	chr1:161692800-161695200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
30	chr1:161693200-161694600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
31	chr1:161693400-161693600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
32	chr1:161693400-161693600	Bivalent Enhancer	Fetal Muscle Trunk	muscle
33	chr1:161693400-161693600	Enhancers	Placenta Amnion	Placenta Amnion
34	chr1:161693400-161693800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
35	chr1:161693400-161693800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
36	chr1:161693400-161693800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
37	chr1:161693600-161694000	Enhancers	HMEC	breast
38	chr1:161693600-161694000	Enhancers	NHEK	skin
39	chr1:161693800-161694000	Enhancers	Fetal Kidney	kidney
40	chr1:161693800-161694600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
41	chr1:161693800-161694800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
42	chr1:161693800-161695000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
43	chr1:161693800-161695400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
44	chr1:161693800-161695400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
45	chr1:161693800-161695400	Weak transcription	Placenta Amnion	Placenta Amnion
46	chr1:161693800-161695600	Enhancers	NHDF-Ad	bronchial
47	chr1:161694000-161695400	Weak transcription	HMEC	breast
48	chr1:161694000-161695400	Weak transcription	NHEK	skin
49	chr1:161694600-161694800	Enhancers	Osteobl	bone
50	chr1:161694600-161695400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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