Variant report

Variant	nsv1004364
Chromosome Location	chr4:48961611-49083089
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:846)
CpG islands
(count:858)
Chromatin interactive
region (count:37)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:846 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:48965071-48965451	K562	blood:	n/a	n/a
2	ARID3A	chr4:48965068-48965466	HepG2	liver:	n/a	n/a
3	ATF1	chr4:48965057-48965395	K562	blood:	n/a	n/a
4	ATF2	chr4:48965089-48965501	GM12878	blood:	n/a	n/a
5	ATF3	chr4:48965187-48965378	H1-hESC	embryonic stem cell:	n/a	n/a
6	BATF	chr4:48965160-48965364	GM12878	blood:	n/a	n/a
7	BCLAF1	chr4:48965055-48965492	GM12878	blood:	n/a	n/a
8	BHLHE40	chr4:48965087-48965437	GM12878	blood:	n/a	chr4:48965224-48965240
9	BHLHE40	chr4:48965128-48965371	K562	blood:	n/a	chr4:48965224-48965240
10	BRCA1	chr4:48965068-48965359	Hela-S3	cervix:	n/a	n/a
11	CEBPB	chr4:49034404-49034777	K562	blood:	n/a	chr4:49034607-49034618
12	CEBPB	chr4:48970879-48971148	H1-hESC	embryonic stem cell:	n/a	n/a
13	CEBPB	chr4:49020904-49021000	A549	lung:	n/a	chr4:49020962-49020973
14	CEBPB	chr4:48965176-48965380	A549	lung:	n/a	n/a
15	CEBPB	chr4:48970709-48971357	HCT-116	colon:	n/a	n/a
16	CEBPB	chr4:48975524-48975806	K562	blood:	n/a	chr4:48975788-48975799
17	CEBPB	chr4:49034479-49034768	ECC-1	luminal epithelium:	n/a	chr4:49034607-49034618
18	CEBPB	chr4:48975652-48975931	HepG2	liver:	n/a	chr4:48975788-48975799
19	CEBPB	chr4:48970945-48971119	K562	blood:	n/a	n/a
20	CEBPB	chr4:49034427-49034820	MCF-7	breast:	n/a	chr4:49034607-49034618
21	CEBPB	chr4:48984066-48984268	K562	blood:	n/a	chr4:48984158-48984169
22	CEBPB	chr4:49034477-49034777	IMR90	lung:	n/a	chr4:49034607-49034618
23	CEBPB	chr4:49034389-49034885	A549	lung:	n/a	chr4:49034607-49034618
24	CEBPB	chr4:49045200-49045225	HepG2	liver:	n/a	chr4:49045204-49045215
25	CEBPB	chr4:48970834-48971287	ECC-1	luminal epithelium:	n/a	n/a
26	CEBPB	chr4:49020953-49021002	K562	blood:	n/a	chr4:49020962-49020973
27	CEBPB	chr4:48965132-48965440	Hela-S3	cervix:	n/a	n/a
28	CEBPB	chr4:48969703-48969903	A549	lung:	n/a	chr4:48969795-48969806
29	CEBPB	chr4:49034505-49034753	HepG2	liver:	n/a	chr4:49034607-49034618
30	CEBPB	chr4:49082855-49083049	IMR90	lung:	n/a	chr4:49082942-49082951 chr4:49082940-49082951 chr4:49082942-49082953
31	CEBPB	chr4:48970838-48971337	HCT-116	colon:	n/a	n/a
32	CEBPB	chr4:48969699-48969938	Hela-S3	cervix:	n/a	chr4:48969795-48969806
33	CEBPB	chr4:49034462-49034774	HepG2	liver:	n/a	chr4:49034607-49034618
34	CEBPB	chr4:49082949-49082960	A549	lung:	n/a	n/a
35	CEBPB	chr4:48970730-48971280	IMR90	lung:	n/a	n/a
36	CEBPB	chr4:48970882-48971196	Hela-S3	cervix:	n/a	n/a
37	CEBPB	chr4:48969702-48969900	K562	blood:	n/a	chr4:48969795-48969806
38	CEBPB	chr4:49034435-49034795	K562	blood:	n/a	chr4:49034607-49034618
39	CEBPB	chr4:48970879-48971121	A549	lung:	n/a	n/a
40	CEBPB	chr4:49034451-49034802	A549	lung:	n/a	chr4:49034607-49034618
41	CEBPB	chr4:48984018-48984328	HepG2	liver:	n/a	chr4:48984158-48984169
42	CEBPB	chr4:48970762-48971277	MCF-7	breast:	n/a	n/a
43	CEBPB	chr4:48969546-48970070	ECC-1	luminal epithelium:	n/a	chr4:48969795-48969806
44	CEBPB	chr4:49034476-49034725	K562	blood:	n/a	chr4:49034607-49034618
45	CEBPB	chr4:49034546-49034709	HepG2	liver:	n/a	chr4:49034607-49034618
46	CEBPB	chr4:48969639-48969924	HepG2	liver:	n/a	chr4:48969795-48969806
47	CEBPB	chr4:49034494-49034836	ECC-1	luminal epithelium:	n/a	chr4:49034607-49034618
48	CEBPB	chr4:48977072-48977179	Hela-S3	cervix:	n/a	n/a
49	CEBPB	chr4:48970901-48971258	MCF-7	breast:	n/a	n/a
50	CEBPB	chr4:49034470-49034787	HepG2	liver:	n/a	chr4:49034607-49034618

(count:858 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:48987024-48987074	PANC-1	pancreas:	n/a
2	chr4:48988015-48988065	HAEpiC	amniotic membrane:	n/a
3	chr4:48984176-48984226	MCF-7	breast:	n/a
4	chr4:48988321-48988371	T-47D	breast:	n/a
5	chr4:48987024-48987074	PANC-1	pancreas:	n/a
6	chr4:48988015-48988065	HAEpiC	amniotic membrane:	n/a
7	chr4:48984176-48984226	MCF-7	breast:	n/a
8	chr4:48988321-48988371	T-47D	breast:	n/a
9	chr4:48988801-48988851	NB4	blood:	n/a
10	chr4:48987024-48987074	HRPEpiC	eye:	n/a
11	chr4:48988090-48988140	NB4	blood:	n/a
12	chr4:48990530-48990580	PANC-1	pancreas:	n/a
13	chr4:48988015-48988065	HUVEC	blood vessel:	n/a
14	chr4:48988090-48988140	AoSMC	blood vessel:	n/a
15	chr4:48988801-48988851	HMEC	breast:	n/a
16	chr4:48991973-48992023	HCPEpiC	choroid plexus:	n/a
17	chr4:48987791-48987841	HCM	heart:	n/a
18	chr4:48984176-48984226	NH-A	brain:	n/a
19	chr4:48988038-48988088	AG10803	skin:	n/a
20	chr4:48984176-48984226	SK-N-SH	brain:	n/a
21	chr4:48988321-48988371	IMR90	lung:	fetal
22	chr4:48988038-48988088	HMEC	breast:	n/a
23	chr4:48987791-48987841	HMEC	breast:	n/a
24	chr4:48988801-48988851	SKMC	muscle:	n/a
25	chr4:48988090-48988140	HCF	heart:	n/a
26	chr4:48990530-48990580	PFSK-1	brain:	n/a
27	chr4:48970898-48970948	K562	blood:	n/a
28	chr4:48988090-48988140	GM12891	blood:	n/a
29	chr4:48988038-48988088	ProgFib	skin:	n/a
30	chr4:48988066-48988116	PFSK-1	brain:	n/a
31	chr4:48991973-48992023	HCF	heart:	n/a
32	chr4:48984176-48984226	ECC-1	luminal epithelium:	n/a
33	chr4:48988090-48988140	Hela-S3	cervix:	n/a
34	chr4:48984176-48984226	GM12892	blood:	n/a
35	chr4:48988015-48988065	HCM	heart:	n/a
36	chr4:48990530-48990580	SK-N-MC	brain:	n/a
37	chr4:48988253-48988303	HAEpiC	amniotic membrane:	n/a
38	chr4:48990530-48990580	NB4	blood:	n/a
39	chr4:48988124-48988174	SK-N-SH	brain:	n/a
40	chr4:48988253-48988303	HepG2	liver:	n/a
41	chr4:48988066-48988116	LNCaP	prostate:	n/a
42	chr4:48988090-48988140	A549	lung:	n/a
43	chr4:48988321-48988371	NHDF-neo	bronchial:	n/a
44	chr4:48987024-48987074	Hepatocyte	liver:	n/a
45	chr4:48991973-48992023	AG10803	skin:	n/a
46	chr4:48988038-48988088	T-47D	breast:	n/a
47	chr4:48991973-48992023	U87	brain:	n/a
48	chr4:48970898-48970948	HPAEpiC	pulmonary alveolar:	n/a
49	chr4:48988090-48988140	SK-N-SH	brain:	n/a
50	chr4:48988015-48988065	H1-hESC	embryonic stem cell:	embryo

(count:37 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:48965209..48965738-chr4:49030225..49031079,2	MCF-7	breast:
2	chr4:48998219..48999902-chr4:49007449..49009207,2	K562	blood:
3	chr4:48946670..48947329-chr4:48964846..48965527,2	MCF-7	breast:
4	chr4:48965278..48967505-chr4:48968176..48969778,2	K562	blood:
5	chr4:48973617..48975284-chr4:48977428..48979706,2	K562	blood:
6	chr4:48993956..48996256-chr4:49000276..49001827,2	K562	blood:
7	chr4:49061609..49064062-chr4:49065907..49068777,2	K562	blood:
8	chr4:48908204..48910120-chr4:48962390..48964503,2	MCF-7	breast:
9	chr4:48945137..48946034-chr4:48964617..48965701,8	MCF-7	breast:
10	chr4:48965278..48967505-chr4:48968176..48969778,2	K562	blood:
11	chr4:48580097..48581053-chr4:48964810..48965685,4	K562	blood:
12	chr1:55352442..55353197-chr4:49034365..49034935,2	MCF-7	breast:
13	chr4:48964805..48966894-chr4:48969035..48971406,2	K562	blood:
14	chr4:48998219..48999902-chr4:49007449..49009207,2	K562	blood:
15	chr4:48964805..48966894-chr4:48969035..48971406,2	K562	blood:
16	chr4:48854871..48855704-chr4:48963569..48964287,2	MCF-7	breast:
17	chr4:49061609..49064062-chr4:49065907..49068777,2	K562	blood:
18	chr4:48987005..48989182-chr4:48992277..48994580,2	K562	blood:
19	chr4:48579844..48581461-chr4:48964715..48966249,12	MCF-7	breast:
20	chr4:48580146..48580771-chr4:48964761..48965396,2	MCF-7	breast:
21	chr4:48977539..48979962-chr4:48981392..48983640,2	MCF-7	breast:
22	chr4:48977539..48979962-chr4:48981392..48983640,2	MCF-7	breast:
23	chr4:48946653..48948896-chr4:48958919..48961929,3	MCF-7	breast:
24	chr4:48949886..48950504-chr4:48964760..48965282,2	K562	blood:
25	chr4:48908075..48909818-chr4:48968023..48970004,2	MCF-7	breast:
26	chr4:48965085..48965843-chr4:49034216..49034787,2	MCF-7	breast:
27	chr4:48906931..48910301-chr4:48958614..48962383,3	MCF-7	breast:
28	chr4:48973617..48975284-chr4:48977428..48979706,2	K562	blood:
29	chr4:48965085..48965843-chr4:49034216..49034787,2	MCF-7	breast:
30	chr4:48993956..48996256-chr4:49000276..49001827,2	K562	blood:
31	chr4:48949781..48950345-chr4:48964835..48965506,2	MCF-7	breast:
32	chr4:48956823..48958903-chr4:48968215..48971051,2	K562	blood:
33	chr4:48954659..48957086-chr4:48963559..48965076,2	MCF-7	breast:
34	chr4:48949903..48950438-chr4:48964755..48965374,2	MCF-7	breast:
35	chr4:48942645..48943396-chr4:48965081..48965603,2	MCF-7	breast:
36	chr4:48950948..48952452-chr4:48963700..48966587,2	MCF-7	breast:
37	chr4:48559190..48559914-chr4:48964738..48965291,2	MCF-7	breast:

No data

Variant related genes	Relation type
TPI1P4	TF binding region
CWH43	TF binding region
TPI1P4	CpG island
CWH43	CpG island
ENSG00000075539	chromatin interactions
ENSG00000145247	chromatin interactions
ENSG00000109182	chromatin interactions
ENSG00000242396	chromatin interactions
ENSG00000116133	chromatin interactions

Extended variants
information (count: 4006 )
Associated
traits (count: 65 )

Variant overlapped rSNPs/rCNVs (count:4006 , 50 per page) page: 1 2 3 4 5 6 7 ... 81

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs191409851	chr4:48961625-48961626	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs537275407	chr4:48961635-48961636	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs555948095	chr4:48961648-48961649	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs566790907	chr4:48961697-48961698	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs116457876	chr4:48961698-48961699	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs183730176	chr4:48961731-48961732	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs34745493	chr4:48961748-48961749	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs371922751	chr4:48961786-48961787	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs551419032	chr4:48961811-48961812	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs115825178	chr4:48961831-48961832	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs116217477	chr4:48961839-48961840	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs188659801	chr4:48961898-48961899	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs563472459	chr4:48961914-48961915	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs192447312	chr4:48961942-48961943	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs534145340	chr4:48961958-48961959	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs151163988	chr4:48961965-48961966	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs36000385	chr4:48961970-48961971	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs115253384	chr4:48961980-48961981	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs183520284	chr4:48962096-48962097	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs551194141	chr4:48962111-48962112	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs369775359	chr4:48962113-48962114	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs76159413	chr4:48962129-48962130	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs186756818	chr4:48962176-48962177	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs375006742	chr4:48962182-48962183	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs112261500	chr4:48962257-48962258	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs140129616	chr4:48962263-48962264	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs570224281	chr4:48962270-48962271	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs138167941	chr4:48962275-48962276	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs141065414	chr4:48962276-48962277	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs369835895	chr4:48962302-48962303	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs207464684	chr4:48962313-48962314	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs567520871	chr4:48962320-48962321	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs184588966	chr4:48962323-48962324	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs144787700	chr4:48962350-48962351	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs77605193	chr4:48962355-48962356	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs559072339	chr4:48962357-48962358	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs138641694	chr4:48962384-48962385	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs115874314	chr4:48962414-48962415	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs538382880	chr4:48962433-48962434	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs189912216	chr4:48962499-48962500	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs542918144	chr4:48962502-48962503	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs149594076	chr4:48962504-48962505	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs573122211	chr4:48962511-48962512	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs540321758	chr4:48962522-48962523	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs114485256	chr4:48962611-48962612	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs375139342	chr4:48962639-48962640	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs556358572	chr4:48962643-48962644	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs377337384	chr4:48962673-48962674	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs192850322	chr4:48962685-48962686	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs574809503	chr4:48962731-48962732	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:65)

Disease	PMID	Source
Colorectal cancer	19359472	CNVD
Neuroblastoma	17533364	CNVD
Oral squamous cell carcinoma	17134496	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Cancer	21637783	CNVD
Melanoma	21693616	CNVD
Squamous cell cancer	21044232	CNVD
Colorectal cancer	20709793	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Non-small cell lung cancer	21044232	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	17387387	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Cervical cancer	21062161	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Glioblastoma multiforme	21080181	CNVD
Chordoma	21602918	CNVD
HIV/AIDS	22032296	CNVD
Medulloblastoma	21979893	CNVD
Neuroblastoma	18923191	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	21858162	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Gastric cancer	21586687	CNVD
lymphocytic leukemia	21291569	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Non-small cell lung cancer	21829676	CNVD
Melanoma	22183965	CNVD
Cancer	22183965	CNVD
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Lung cancer	18438408	CNVD
Renal cell carcinoma	18194544	CNVD
Breast cancer	17603634	CNVD
Glioblastoma multiforme	21922591	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Parkinson disease	21956041	CNVD
Mental retardation	20522426	CNVD
delayed speech	20522426	CNVD
growth disorder	20522426	CNVD
Hepatocellular carcinoma	16750200	CNVD
Myxofibrosarcoma	16751306	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Acute myeloid leukemia	20729466	CNVD
Parkinson disease	18923514	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Cancer	21183584	CNVD
small cell lung cancer	20016488	CNVD
Myelofibrosis	22110671	CNVD
Schizophrenia	21399695	CNVD
Breast cancer	16272173	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	21509527	CNVD

Chromatin state (count:401 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:48956600-48967600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr4:48957400-48964000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
3	chr4:48958400-48962400	Weak transcription	HMEC	breast
4	chr4:48959800-48972400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
5	chr4:48960000-48964400	Weak transcription	Placenta Amnion	Placenta Amnion
6	chr4:48960600-48964200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
7	chr4:48960800-48963600	Enhancers	NHEK	skin
8	chr4:48961200-48961800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
9	chr4:48961400-48961800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
10	chr4:48961400-48964600	Weak transcription	Placenta	Placenta
11	chr4:48961600-48965000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
12	chr4:48961800-48963400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
13	chr4:48962400-48964000	Enhancers	HMEC	breast
14	chr4:48962800-48969000	Weak transcription	Esophagus	oesophagus
15	chr4:48963200-48963600	Enhancers	iPS-20b Cell Line	embryonic stem cell
16	chr4:48963400-48963800	Enhancers	H1 Cell Line	embryonic stem cell
17	chr4:48963400-48963800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
18	chr4:48963400-48964000	Enhancers	iPS-18 Cell Line	embryonic stem cell
19	chr4:48963600-48969000	Weak transcription	NHEK	skin
20	chr4:48963800-48964200	Enhancers	iPS-20b Cell Line	embryonic stem cell
21	chr4:48963800-48964600	Weak transcription	H1 Cell Line	embryonic stem cell
22	chr4:48963800-48969000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
23	chr4:48964000-48964200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
24	chr4:48964000-48969000	Weak transcription	HMEC	breast
25	chr4:48964200-48964600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
26	chr4:48964400-48964800	Enhancers	Placenta Amnion	Placenta Amnion
27	chr4:48964600-48964800	Enhancers	H1 Cell Line	embryonic stem cell
28	chr4:48964600-48964800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
29	chr4:48964600-48965000	Enhancers	Placenta	Placenta
30	chr4:48964600-48965200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
31	chr4:48964600-48965200	Enhancers	Fetal Kidney	kidney
32	chr4:48964800-48966600	Weak transcription	Placenta Amnion	Placenta Amnion
33	chr4:48964800-48967600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
34	chr4:48965000-48969000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
35	chr4:48965200-48969600	Weak transcription	Fetal Kidney	kidney
36	chr4:48966600-48968200	Enhancers	Placenta Amnion	Placenta Amnion
37	chr4:48967600-48967800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
38	chr4:48967600-48968200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
39	chr4:48968200-48968600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
40	chr4:48968200-48969400	Weak transcription	Placenta Amnion	Placenta Amnion
41	chr4:48968400-48970200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
42	chr4:48968400-48970400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
43	chr4:48968600-48970800	Enhancers	Cortex derived primary cultured neurospheres	brain
44	chr4:48968600-48973200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
45	chr4:48968800-48970200	Enhancers	Brain Anterior Caudate	brain
46	chr4:48968800-48970400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
47	chr4:48969000-48969400	Enhancers	Esophagus	oesophagus
48	chr4:48969000-48969400	Enhancers	NH-A	brain
49	chr4:48969000-48972200	Enhancers	NHEK	skin
50	chr4:48969000-48972800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

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