Variant report

Variant	nsv583594
Chromosome Location	chr2:168461161-168597986
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	chr2:168590304-168590631	HepG2	liver:	n/a	n/a
2	BHLHE40	chr2:168508086-168508467	HepG2	liver:	n/a	n/a
3	CEBPB	chr2:168497976-168498270	IMR90	lung:	n/a	chr2:168498090-168498101 chr2:168498090-168498099 chr2:168498088-168498099
4	CEBPB	chr2:168497931-168498266	A549	lung:	n/a	chr2:168498090-168498101 chr2:168498090-168498099 chr2:168498088-168498099
5	CEBPB	chr2:168558757-168559051	MCF-7	breast:	n/a	chr2:168558953-168558966 chr2:168558953-168558964 chr2:168558955-168558966 chr2:168558955-168558964 chr2:168558955-168558964 chr2:168558953-168558966 chr2:168558955-168558964 chr2:168558955-168558964
6	CEBPB	chr2:168543496-168543665	HepG2	liver:	n/a	chr2:168543595-168543606
7	CEBPB	chr2:168563333-168563679	IMR90	lung:	n/a	chr2:168563515-168563526 chr2:168563503-168563514
8	CEBPB	chr2:168563346-168563669	H1-hESC	embryonic stem cell:	n/a	chr2:168563515-168563526 chr2:168563503-168563514
9	CEBPB	chr2:168558728-168559141	HepG2	liver:	n/a	chr2:168558953-168558966 chr2:168558953-168558964 chr2:168558955-168558966 chr2:168558955-168558964 chr2:168558741-168558753 chr2:168558955-168558964 chr2:168558953-168558966 chr2:168558955-168558964 chr2:168558955-168558964
10	CEBPB	chr2:168563341-168563663	Hela-S3	cervix:	n/a	chr2:168563515-168563526 chr2:168563503-168563514
11	CEBPB	chr2:168551372-168551587	HepG2	liver:	n/a	n/a
12	CEBPB	chr2:168563421-168563585	HepG2	liver:	n/a	chr2:168563515-168563526 chr2:168563503-168563514
13	CEBPB	chr2:168503829-168504152	HepG2	liver:	n/a	chr2:168503998-168504009 chr2:168503997-168504010 chr2:168503997-168504010
14	CEBPB	chr2:168558718-168559130	IMR90	lung:	n/a	chr2:168558953-168558966 chr2:168558953-168558964 chr2:168558955-168558966 chr2:168558955-168558964 chr2:168558741-168558753 chr2:168558955-168558964 chr2:168558953-168558966 chr2:168558955-168558964 chr2:168558955-168558964
15	CEBPB	chr2:168563334-168563729	HepG2	liver:	n/a	chr2:168563515-168563526 chr2:168563503-168563514
16	CEBPB	chr2:168563312-168563736	ECC-1	luminal epithelium:	n/a	chr2:168563515-168563526 chr2:168563503-168563514
17	CEBPB	chr2:168503865-168504125	A549	lung:	n/a	chr2:168503998-168504009 chr2:168503997-168504010 chr2:168503997-168504010
18	CEBPB	chr2:168580499-168580813	K562	blood:	n/a	chr2:168580651-168580664 chr2:168580652-168580663 chr2:168580653-168580662
19	CEBPB	chr2:168503912-168504129	K562	blood:	n/a	chr2:168503998-168504009 chr2:168503997-168504010 chr2:168503997-168504010
20	CEBPB	chr2:168558769-168559123	K562	blood:	n/a	chr2:168558953-168558966 chr2:168558953-168558964 chr2:168558955-168558966 chr2:168558955-168558964 chr2:168558955-168558964 chr2:168558953-168558966 chr2:168558955-168558964 chr2:168558955-168558964
21	CEBPB	chr2:168548862-168548990	A549	lung:	n/a	chr2:168548926-168548939
22	CEBPB	chr2:168580492-168580794	HepG2	liver:	n/a	chr2:168580651-168580664 chr2:168580652-168580663 chr2:168580653-168580662
23	CEBPB	chr2:168517567-168517613	HepG2	liver:	n/a	chr2:168517582-168517593 chr2:168517583-168517592
24	CEBPB	chr2:168548788-168549051	IMR90	lung:	n/a	chr2:168548926-168548939
25	CEBPB	chr2:168563287-168563620	HepG2	liver:	n/a	chr2:168563515-168563526 chr2:168563503-168563514
26	CEBPB	chr2:168551434-168551561	H1-hESC	embryonic stem cell:	n/a	n/a
27	CEBPB	chr2:168503861-168504147	IMR90	lung:	n/a	chr2:168503998-168504009 chr2:168503997-168504010 chr2:168503997-168504010
28	CEBPB	chr2:168497944-168498269	HepG2	liver:	n/a	chr2:168498090-168498101 chr2:168498090-168498099 chr2:168498088-168498099
29	CEBPB	chr2:168590304-168590531	HepG2	liver:	n/a	n/a
30	CEBPB	chr2:168553749-168554823	H1-hESC	embryonic stem cell:	n/a	chr2:168554662-168554673 chr2:168554440-168554453 chr2:168554440-168554453 chr2:168554442-168554451 chr2:168554440-168554451
31	CEBPB	chr2:168466857-168467122	A549	lung:	n/a	chr2:168466947-168466958 chr2:168466945-168466958
32	CEBPB	chr2:168563338-168563703	HepG2	liver:	n/a	chr2:168563515-168563526 chr2:168563503-168563514
33	CEBPB	chr2:168558779-168559105	H1-hESC	embryonic stem cell:	n/a	chr2:168558953-168558966 chr2:168558953-168558964 chr2:168558955-168558966 chr2:168558955-168558964 chr2:168558955-168558964 chr2:168558953-168558966 chr2:168558955-168558964 chr2:168558955-168558964
34	CEBPB	chr2:168558749-168559115	A549	lung:	n/a	chr2:168558953-168558966 chr2:168558953-168558964 chr2:168558955-168558966 chr2:168558955-168558964 chr2:168558955-168558964 chr2:168558953-168558966 chr2:168558955-168558964 chr2:168558955-168558964
35	CEBPB	chr2:168548747-168549066	HepG2	liver:	n/a	chr2:168548926-168548939
36	CEBPB	chr2:168580518-168580785	A549	lung:	n/a	chr2:168580651-168580664 chr2:168580652-168580663 chr2:168580653-168580662
37	CEBPB	chr2:168563289-168563710	ECC-1	luminal epithelium:	n/a	chr2:168563515-168563526 chr2:168563503-168563514
38	CHD2	chr2:168545954-168546236	H1-hESC	embryonic stem cell:	n/a	n/a
39	CTCF	chr2:168546018-168546170	Medullo	brain:	n/a	n/a
40	CTCF	chr2:168546001-168546199	HepG2	liver:	n/a	n/a
41	CTCF	chr2:168546000-168546150	HBMEC	blood vessel:	n/a	n/a
42	CTCF	chr2:168572530-168572673	K562	blood:	n/a	n/a
43	CTCF	chr2:168540107-168540198	ProgFib	skin:	n/a	n/a
44	CTCF	chr2:168546080-168546230	HVMF	connective:	n/a	n/a
45	CTCF	chr2:168546000-168546150	AG04449	skin:	n/a	n/a
46	CTCF	chr2:168546120-168546270	A549	lung:	n/a	n/a
47	CTCF	chr2:168546040-168546190	MCF-7	breast:	n/a	n/a
48	CTCF	chr2:168546220-168546370	HCFaa	heart:	n/a	n/a
49	CTCF	chr2:168546020-168546170	WERI-Rb-1	eye:	n/a	n/a
50	CTCF	chr2:168546020-168546170	GM12872	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:168525214-168525264	NHBE	bronchial:	n/a
2	chr2:168589499-168589549	NHBE	bronchial:	n/a
3	chr2:168572517-168572567	AG09309	skin:	n/a
4	chr2:168525214-168525264	U87	brain:	n/a
5	chr2:168572814-168572864	AG10803	skin:	n/a
6	chr2:168572517-168572567	HepG2	liver:	n/a
7	chr2:168570439-168570489	CMK	blood:	n/a
8	chr2:168572517-168572567	AG04450	lung:	fetal
9	chr2:168572728-168572778	A549	lung:	n/a
10	chr2:168570439-168570489	HL-60	blood:	n/a
11	chr2:168463973-168464023	MCF-7	breast:	n/a
12	chr2:168572517-168572567	BE2_C	brain:	n/a
13	chr2:168575200-168575250	U87	brain:	n/a
14	chr2:168570439-168570489	HAEpiC	amniotic membrane:	n/a
15	chr2:168463973-168464023	CMK	blood:	n/a
16	chr2:168572563-168572613	HIPEpiC	eye:	n/a
17	chr2:168572563-168572613	K562	blood:	n/a
18	chr2:168572728-168572778	HIPEpiC	eye:	n/a
19	chr2:168463973-168464023	BE2_C	brain:	n/a
20	chr2:168572728-168572778	HRE	kidney:	n/a
21	chr2:168572517-168572567	AG04449	skin:	fetal
22	chr2:168589499-168589549	AoSMC	blood vessel:	n/a
23	chr2:168525214-168525264	NB4	blood:	n/a
24	chr2:168575200-168575250	Hepatocyte	liver:	n/a
25	chr2:168525214-168525264	Hepatocyte	liver:	n/a
26	chr2:168572814-168572864	HAEpiC	amniotic membrane:	n/a
27	chr2:168575200-168575250	HNPCEpiC	eye:	n/a
28	chr2:168554345-168554395	HepG2	liver:	n/a
29	chr2:168589499-168589549	HCM	heart:	n/a
30	chr2:168554345-168554395	MCF-7	breast:	n/a
31	chr2:168554345-168554395	AG10803	skin:	n/a
32	chr2:168554345-168554395	GM19239	blood:	n/a
33	chr2:168589499-168589549	CMK	blood:	n/a
34	chr2:168572728-168572778	HCPEpiC	choroid plexus:	n/a
35	chr2:168572563-168572613	HEK293	kidney:	embryo
36	chr2:168572728-168572778	NHBE	bronchial:	n/a
37	chr2:168572814-168572864	HUVEC	blood vessel:	n/a
38	chr2:168463973-168464023	Hepatocyte	liver:	n/a
39	chr2:168572814-168572864	HepG2	liver:	n/a
40	chr2:168570439-168570489	AG04450	lung:	fetal
41	chr2:168570439-168570489	HCPEpiC	choroid plexus:	n/a
42	chr2:168463973-168464023	U87	brain:	n/a
43	chr2:168572728-168572778	SAEC	small airway:	n/a
44	chr2:168554345-168554395	GM12891	blood:	n/a
45	chr2:168572563-168572613	A549	lung:	n/a
46	chr2:168525214-168525264	A549	lung:	n/a
47	chr2:168575200-168575250	HepG2	liver:	n/a
48	chr2:168589499-168589549	NHDF-neo	bronchial:	n/a
49	chr2:168572563-168572613	MCF-7	breast:	n/a
50	chr2:168572563-168572613	MCF10A-Er-Src	breast:	n/a

No.	Distal block	Cell Line	Cell type
1	chr2:168534742..168537162-chr2:168545457..168548384,2	K562	blood:
2	chr2:168564278..168566007-chr2:168567964..168569747,3	K562	blood:
3	chr2:168584586..168586912-chr2:168590277..168592484,2	K562	blood:
4	chr2:168569700..168571629-chr2:168574567..168576209,2	K562	blood:
5	chr2:168511059..168513910-chr2:168515507..168517847,2	K562	blood:
6	chr2:168569700..168571629-chr2:168574567..168576209,2	K562	blood:
7	chr2:168582986..168586218-chr2:168596539..168599402,3	K562	blood:
8	chr2:168584586..168586912-chr2:168590277..168592484,2	K562	blood:
9	chr2:168553081..168556581-chr2:168557540..168560778,3	MCF-7	breast:
10	chr2:168432443..168434147-chr2:168458240..168461184,2	K562	blood:
11	chr2:168412011..168414014-chr2:168467499..168469834,2	K562	blood:
12	chr2:168597601..168599335-chr2:168787943..168789534,2	K562	blood:
13	chr2:168564278..168566007-chr2:168567964..168569747,3	K562	blood:
14	chr2:168511059..168513910-chr2:168515507..168517847,2	K562	blood:
15	chr2:168579362..168581960-chr2:168584319..168587254,2	K562	blood:
16	chr2:168574983..168577056-chr2:168583842..168586098,2	K562	blood:
17	chr2:168553081..168556581-chr2:168557540..168560778,3	MCF-7	breast:
18	chr2:168582986..168586218-chr2:168596539..168599402,3	K562	blood:
19	chr2:168574983..168577056-chr2:168583842..168586098,2	K562	blood:
20	chr2:168579362..168581960-chr2:168584319..168587254,2	K562	blood:
21	chr2:168534742..168537162-chr2:168545457..168548384,2	K562	blood:
22	chr2:168572299..168574457-chr2:168576966..168579466,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-STK39-5	chr2:168505171-168505388	expReg_chr2_12378_-

Variant related genes	Relation type
CTAGE14P	TF binding region
RNU7-148P	TF binding region
CTAGE14P	CpG island
RNU7-148P	CpG island
ENSG00000214211	chromatin interactions

Extended variants
information (count: 4673 )
Associated
traits (count: 52 )

Variant overlapped rSNPs/rCNVs (count:4673 , 50 per page) page: 1 2 3 4 5 6 7 ... 94

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs734284	chr2:168461161-168461162	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs552282386	chr2:168461257-168461258	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs533380651	chr2:168461283-168461284	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs10210297	chr2:168461305-168461306	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs534858169	chr2:168461382-168461383	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs548397606	chr2:168461383-168461384	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs375322391	chr2:168461399-168461400	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs552172377	chr2:168461410-168461411	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs540223761	chr2:168461446-168461447	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs575380451	chr2:168461461-168461462	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs537297130	chr2:168461465-168461466	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs556619744	chr2:168461477-168461478	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs891741	chr2:168461505-168461506	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs538642517	chr2:168461516-168461517	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs142594331	chr2:168461553-168461554	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs191834939	chr2:168461554-168461555	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs541235616	chr2:168461594-168461595	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs78472584	chr2:168461616-168461617	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs370302428	chr2:168461636-168461637	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs574812859	chr2:168461638-168461639	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs891742	chr2:168461673-168461674	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
22	rs183460929	chr2:168461714-168461715	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs146792131	chr2:168461727-168461728	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs551879110	chr2:168461762-168461763	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs735424	chr2:168461784-168461785	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs528155389	chr2:168461806-168461807	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs548411572	chr2:168461808-168461809	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs111795371	chr2:168461847-168461848	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs372419858	chr2:168461861-168461862	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs76096672	chr2:168461879-168461880	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs550887223	chr2:168461912-168461913	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs570634213	chr2:168461931-168461932	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs368351751	chr2:168461950-168461951	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs138876148	chr2:168461968-168461969	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs565838100	chr2:168461991-168461992	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs550481547	chr2:168461995-168461996	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs5836148	chr2:168461996-168461997	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs534765030	chr2:168462003-168462004	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs554756547	chr2:168462005-168462006	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs574723385	chr2:168462038-168462039	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs543585613	chr2:168462063-168462064	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs149281023	chr2:168462066-168462067	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs143494359	chr2:168462087-168462088	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs78467065	chr2:168462196-168462197	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs113817936	chr2:168462217-168462218	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs115630824	chr2:168462253-168462254	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs185900410	chr2:168462329-168462330	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs561752020	chr2:168462343-168462344	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs147994418	chr2:168462355-168462356	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs111445147	chr2:168462427-168462428	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:52)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	21979893	CNVD
Ependymoma	16718352	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Autism	22495311	CNVD
Autism	18522746	CNVD
Neurodevelopmental disorder	22521361	CNVD
Melanoma	18172304	CNVD
Cancer	16751803	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Seminomas	18059402	CNVD
Testicular germ cell tumor	18059402	CNVD
Breast cancer	16272173	CNVD
Ewing''s sarcoma	17952124	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Autism	16446308	CNVD
Autism	19401682	CNVD
Colorectal cancer	16272173	CNVD
myoclonus epilepsy	18472482	CNVD
Benign familial neonatal-infantile seizures	18472482	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Lung cancer	18438408	CNVD
Mental retardation	22214275	CNVD
Glioblastoma	21080181	CNVD
small cell lung cancer	20016488	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Autism	18414403	CNVD
Developmental delay	21147756	CNVD
Prostate cancer	16573809	CNVD
Myelofibrosis	22110671	CNVD
Neonatal seizures	20384724	CNVD
severe myoclonic epilepsy of infancy	18294202	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Prostate cancer	18632612	CNVD
Pancreatic cancer	17952125	CNVD
Amyotrophic lateral sclerosis	20685689	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:354 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:168452600-168463400	Weak transcription	Cortex derived primary cultured neurospheres	brain
2	chr2:168458400-168463800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
3	chr2:168462400-168464600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
4	chr2:168463200-168464400	Enhancers	iPS-18 Cell Line	embryonic stem cell
5	chr2:168463400-168464200	Enhancers	Breast Myoepithelial Primary Cells	Breast
6	chr2:168463400-168464600	Enhancers	Cortex derived primary cultured neurospheres	brain
7	chr2:168463800-168464200	Enhancers	H1 Cell Line	embryonic stem cell
8	chr2:168463800-168464200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
9	chr2:168463800-168464200	Enhancers	iPS-15b Cell Line	embryonic stem cell
10	chr2:168463800-168464200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
11	chr2:168463800-168464200	Enhancers	Fetal Brain Male	brain
12	chr2:168463800-168464400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
13	chr2:168463800-168464600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
14	chr2:168463800-168464600	Enhancers	HUES6 Cell Line	embryonic stem cell
15	chr2:168463800-168464600	Enhancers	iPS-20b Cell Line	embryonic stem cell
16	chr2:168463800-168464600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
17	chr2:168464000-168464600	Enhancers	Brain Germinal Matrix	brain
18	chr2:168464200-168476600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
19	chr2:168464600-168473600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
20	chr2:168464600-168474200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
21	chr2:168464800-168465400	Enhancers	HepG2	liver
22	chr2:168473600-168474200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
23	chr2:168473600-168474600	Enhancers	HUES48 Cell Line	embryonic stem cell
24	chr2:168474200-168474600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
25	chr2:168474200-168476200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
26	chr2:168476200-168476800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
27	chr2:168476600-168476800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
28	chr2:168476800-168480800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
29	chr2:168482200-168485200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
30	chr2:168490600-168507600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
31	chr2:168493600-168507600	Weak transcription	Cortex derived primary cultured neurospheres	brain
32	chr2:168502200-168504800	Weak transcription	HUES48 Cell Line	embryonic stem cell
33	chr2:168503000-168504400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
34	chr2:168503400-168507600	Weak transcription	HUES64 Cell Line	embryonic stem cell
35	chr2:168503600-168508200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
36	chr2:168503800-168504000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
37	chr2:168504000-168509000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
38	chr2:168504400-168507400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
39	chr2:168504800-168505600	Strong transcription	HUES48 Cell Line	embryonic stem cell
40	chr2:168504800-168508000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
41	chr2:168505600-168508000	Weak transcription	HUES48 Cell Line	embryonic stem cell
42	chr2:168507400-168510400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
43	chr2:168507600-168507800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
44	chr2:168507600-168507800	Enhancers	Cortex derived primary cultured neurospheres	brain
45	chr2:168507600-168508000	Enhancers	Fetal Brain Male	brain
46	chr2:168507600-168508400	Enhancers	HUES64 Cell Line	embryonic stem cell
47	chr2:168507800-168508200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
48	chr2:168507800-168508200	Weak transcription	Cortex derived primary cultured neurospheres	brain
49	chr2:168507800-168509400	Enhancers	HepG2	liver
50	chr2:168508000-168508400	Genic enhancers	HUES48 Cell Line	embryonic stem cell

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