Variant report

Variant	nsv459940
Chromosome Location	chr2:168552363-168628177
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	BACH1	chr2:168618942-168619019	K562	blood:	n/a	n/a
3	BACH1	chr2:168606202-168606504	H1-hESC	embryonic stem cell:	n/a	chr2:168606365-168606379
4	CEBPB	chr2:168616042-168616311	HepG2	liver:	n/a	n/a
5	CEBPB	chr2:168590304-168590531	HepG2	liver:	n/a	n/a
6	CEBPB	chr2:168580492-168580794	HepG2	liver:	n/a	chr2:168580651-168580664 chr2:168580652-168580663 chr2:168580653-168580662
7	CEBPB	chr2:168602588-168602776	HepG2	liver:	n/a	chr2:168602687-168602698 chr2:168602686-168602699
8	CEBPB	chr2:168563287-168563620	HepG2	liver:	n/a	chr2:168563515-168563526 chr2:168563503-168563514
9	CEBPB	chr2:168605536-168605855	A549	lung:	n/a	n/a
10	CEBPB	chr2:168563346-168563669	H1-hESC	embryonic stem cell:	n/a	chr2:168563515-168563526 chr2:168563503-168563514
11	CEBPB	chr2:168563341-168563663	Hela-S3	cervix:	n/a	chr2:168563515-168563526 chr2:168563503-168563514
12	CEBPB	chr2:168563338-168563703	HepG2	liver:	n/a	chr2:168563515-168563526 chr2:168563503-168563514
13	CEBPB	chr2:168563312-168563736	ECC-1	luminal epithelium:	n/a	chr2:168563515-168563526 chr2:168563503-168563514
14	CEBPB	chr2:168580499-168580813	K562	blood:	n/a	chr2:168580651-168580664 chr2:168580652-168580663 chr2:168580653-168580662
15	CEBPB	chr2:168615989-168616315	H1-hESC	embryonic stem cell:	n/a	n/a
16	CEBPB	chr2:168605540-168605841	IMR90	lung:	n/a	n/a
17	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
18	CEBPB	chr2:168616126-168616241	K562	blood:	n/a	n/a
19	CEBPB	chr2:168617930-168618150	HepG2	liver:	n/a	chr2:168618002-168618013 chr2:168618085-168618098
20	CEBPB	chr2:168580518-168580785	A549	lung:	n/a	chr2:168580651-168580664 chr2:168580652-168580663 chr2:168580653-168580662
21	CEBPB	chr2:168563289-168563710	ECC-1	luminal epithelium:	n/a	chr2:168563515-168563526 chr2:168563503-168563514
22	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
23	CEBPB	chr2:168605536-168605830	Hela-S3	cervix:	n/a	n/a
24	CEBPB	chr2:168625390-168625604	HepG2	liver:	n/a	n/a
25	CEBPB	chr2:168605527-168605885	HepG2	liver:	n/a	n/a
26	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
27	CEBPB	chr2:168563333-168563679	IMR90	lung:	n/a	chr2:168563515-168563526 chr2:168563503-168563514
28	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
29	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
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	chr2:168563334-168563729	HepG2	liver:	n/a	chr2:168563515-168563526 chr2:168563503-168563514
32	CEBPB	chr2:168563421-168563585	HepG2	liver:	n/a	chr2:168563515-168563526 chr2:168563503-168563514
33	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
34	CHD2	chr2:168613031-168613230	H1-hESC	embryonic stem cell:	n/a	n/a
35	CTCF	chr2:168616080-168616230	SK-N-SH_RA	brain:	n/a	n/a
36	CTCF	chr2:168616080-168616230	GM12873	blood:	n/a	n/a
37	CTCF	chr2:168572530-168572673	K562	blood:	n/a	n/a
38	CTCF	chr2:168616140-168616290	HepG2	liver:	n/a	n/a
39	CTCF	chr2:168616100-168616250	SK-N-SH_RA	brain:	n/a	n/a
40	CTCF	chr2:168616173-168616315	MCF-7	breast:	n/a	n/a
41	CTCF	chr2:168616114-168616411	K562	blood:	n/a	n/a
42	CTCF	chr2:168616200-168616350	HRPEpiC	eye:	n/a	n/a
43	CTCF	chr2:168616120-168616270	K562	blood:	n/a	n/a
44	CTCF	chr2:168616200-168616350	Caco-2	colon:	n/a	n/a
45	CTCF	chr2:168616202-168616276	MCF-7	breast:	n/a	n/a
46	CTCF	chr2:168613780-168613801	ProgFib	skin:	n/a	n/a
47	CTCF	chr2:168616120-168616270	MCF-7	breast:	n/a	n/a
48	CTCF	chr2:168616140-168616290	GM12873	blood:	n/a	n/a
49	CTCF	chr2:168616206-168616288	Gliobla	brain:	n/a	n/a
50	CTCF	chr2:168625700-168625850	HepG2	liver:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:168572563-168572613	GM12878	blood:	n/a
2	chr2:168572563-168572613	IMR90	lung:	fetal
3	chr2:168609834-168609884	HCM	heart:	n/a
4	chr2:168554345-168554395	A549	lung:	n/a
5	chr2:168614674-168614724	BE2_C	brain:	n/a
6	chr2:168575200-168575250	NHBE	bronchial:	n/a
7	chr2:168572728-168572778	SAEC	small airway:	n/a
8	chr2:168570439-168570489	AG09309	skin:	n/a
9	chr2:168575200-168575250	HRE	kidney:	n/a
10	chr2:168572728-168572778	SK-N-SH	brain:	n/a
11	chr2:168609834-168609884	CMK	blood:	n/a
12	chr2:168572517-168572567	GM12878	blood:	n/a
13	chr2:168572728-168572778	HIPEpiC	eye:	n/a
14	chr2:168572728-168572778	SKMC	muscle:	n/a
15	chr2:168609834-168609884	SKMC	muscle:	n/a
16	chr2:168572517-168572567	AoSMC	blood vessel:	n/a
17	chr2:168572814-168572864	HPAEpiC	pulmonary alveolar:	n/a
18	chr2:168572728-168572778	HMEC	breast:	n/a
19	chr2:168572728-168572778	A549	lung:	n/a
20	chr2:168572563-168572613	U87	brain:	n/a
21	chr2:168572728-168572778	T-47D	breast:	n/a
22	chr2:168572728-168572778	BE2_C	brain:	n/a
23	chr2:168572814-168572864	HRPEpiC	eye:	n/a
24	chr2:168575200-168575250	GM19239	blood:	n/a
25	chr2:168575200-168575250	SK-N-SH	brain:	n/a
26	chr2:168572517-168572567	SK-N-SH_RA	brain:	n/a
27	chr2:168572728-168572778	HCPEpiC	choroid plexus:	n/a
28	chr2:168614674-168614724	CMK	blood:	n/a
29	chr2:168570439-168570489	ovcar-3	ovarian:	n/a
30	chr2:168570439-168570489	HEEpiC	esophagus:	n/a
31	chr2:168572814-168572864	RPTEC	kidney:	n/a
32	chr2:168614674-168614724	AG04450	lung:	fetal
33	chr2:168572563-168572613	Caco-2	colon:	n/a
34	chr2:168572728-168572778	HRE	kidney:	n/a
35	chr2:168575200-168575250	H1-hESC	embryonic stem cell:	embryo
36	chr2:168570439-168570489	HCM	heart:	n/a
37	chr2:168570439-168570489	LNCaP	prostate:	n/a
38	chr2:168609834-168609884	PFSK-1	brain:	n/a
39	chr2:168589499-168589549	PFSK-1	brain:	n/a
40	chr2:168575200-168575250	Hela-S3	cervix:	n/a
41	chr2:168614674-168614724	IMR90	lung:	fetal
42	chr2:168609834-168609884	NHBE	bronchial:	n/a
43	chr2:168575200-168575250	ProgFib	skin:	n/a
44	chr2:168554345-168554395	AG09319	gingival:	n/a
45	chr2:168589499-168589549	Caco-2	colon:	n/a
46	chr2:168572728-168572778	NB4	blood:	n/a
47	chr2:168572814-168572864	HCT-116	colon:	n/a
48	chr2:168572563-168572613	HCF	heart:	n/a
49	chr2:168609834-168609884	HEK293	kidney:	embryo
50	chr2:168572563-168572613	Hela-S3	cervix:	n/a

No.	Distal block	Cell Line	Cell type
1	chr2:168572299..168574457-chr2:168576966..168579466,2	K562	blood:
2	chr2:168608803..168611110-chr2:168612210..168614300,2	K562	blood:
3	chr2:168574983..168577056-chr2:168583842..168586098,2	K562	blood:
4	chr2:168564278..168566007-chr2:168567964..168569747,3	K562	blood:
5	chr2:168582986..168586218-chr2:168596539..168599402,3	K562	blood:
6	chr2:168574983..168577056-chr2:168583842..168586098,2	K562	blood:
7	chr2:168579362..168581960-chr2:168584319..168587254,2	K562	blood:
8	chr2:168569700..168571629-chr2:168574567..168576209,2	K562	blood:
9	chr2:168569700..168571629-chr2:168574567..168576209,2	K562	blood:
10	chr2:168584586..168586912-chr2:168590277..168592484,2	K562	blood:
11	chr2:168553081..168556581-chr2:168557540..168560778,3	MCF-7	breast:
12	chr2:168617105..168619899-chr2:168623577..168626394,2	K562	blood:
13	chr2:168597601..168599335-chr2:168787943..168789534,2	K562	blood:
14	chr2:168582986..168586218-chr2:168596539..168599402,3	K562	blood:
15	chr2:168584586..168586912-chr2:168590277..168592484,2	K562	blood:
16	chr2:168553081..168556581-chr2:168557540..168560778,3	MCF-7	breast:
17	chr2:168617105..168619899-chr2:168623577..168626394,2	K562	blood:
18	chr2:168564278..168566007-chr2:168567964..168569747,3	K562	blood:
19	chr2:168579362..168581960-chr2:168584319..168587254,2	K562	blood:
20	chr2:168608803..168611110-chr2:168612210..168614300,2	K562	blood:

Variant related genes	Relation type
CTAGE14P	TF binding region
CTAGE14P	CpG island
ENSG00000214211	chromatin interactions

Extended variants
information (count: 2358 )
Associated
traits (count: 53 )

Variant overlapped rSNPs/rCNVs (count:2358 , 50 per page) page: 1 2 3 4 5 6 7 ... 48

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1900834	chr2:168552363-168552364	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs182713077	chr2:168552374-168552375	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs528472233	chr2:168552385-168552386	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs140369833	chr2:168552386-168552387	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs561885089	chr2:168552400-168552401	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs530894997	chr2:168552480-168552481	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs75862326	chr2:168552490-168552491	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs187398374	chr2:168552501-168552502	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs111666045	chr2:168552505-168552506	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs146990532	chr2:168552576-168552577	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs191634139	chr2:168552641-168552642	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs184954278	chr2:168552668-168552669	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs535484812	chr2:168552681-168552682	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs77829413	chr2:168552706-168552707	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs571113795	chr2:168552735-168552736	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs35642042	chr2:168552753-168552754	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs35575073	chr2:168552807-168552808	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs397797830	chr2:168552828-168552829	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs575439849	chr2:168552868-168552869	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs112390631	chr2:168552882-168552883	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs537962080	chr2:168552891-168552892	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs557535807	chr2:168552907-168552908	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs529723252	chr2:168552919-168552920	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs150081953	chr2:168552920-168552921	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs138096439	chr2:168553024-168553025	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs553308591	chr2:168553079-168553080	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs540010270	chr2:168553087-168553088	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs11690497	chr2:168553125-168553126	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs573587038	chr2:168553172-168553173	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs189363153	chr2:168553179-168553180	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs561722943	chr2:168553192-168553193	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs530784685	chr2:168553230-168553231	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs568480669	chr2:168553231-168553232	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs564383134	chr2:168553255-168553256	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs533574523	chr2:168553264-168553265	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs141687975	chr2:168553321-168553322	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs4667541	chr2:168553341-168553342	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs529591003	chr2:168553370-168553371	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs147061200	chr2:168553380-168553381	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs568887194	chr2:168553417-168553418	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs537803213	chr2:168553430-168553431	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs369683401	chr2:168553482-168553483	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs58502451	chr2:168553496-168553497	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs534037272	chr2:168553523-168553524	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs553666950	chr2:168553564-168553565	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs573624009	chr2:168553582-168553583	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs541938815	chr2:168553618-168553619	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs542532716	chr2:168553736-168553737	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs192452185	chr2:168553745-168553746	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs112911902	chr2:168553761-168553762	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:53)

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
Prostate cancer	18632612	CNVD
Pancreatic cancer	17952125	CNVD
Amyotrophic lateral sclerosis	20685689	CNVD
Breast cancer	22522925	CNVD
Glioma	20126413	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:400 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:168542400-168563600	Weak transcription	Cortex derived primary cultured neurospheres	brain
2	chr2:168547400-168553000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
3	chr2:168547400-168553200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
4	chr2:168549600-168553800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
5	chr2:168552200-168552400	Enhancers	Duodenum Mucosa	Duodenum
6	chr2:168552800-168553600	Enhancers	HUES48 Cell Line	embryonic stem cell
7	chr2:168552800-168554000	Enhancers	HUES64 Cell Line	embryonic stem cell
8	chr2:168553000-168553800	Enhancers	iPS-15b Cell Line	embryonic stem cell
9	chr2:168553200-168553800	Enhancers	HUES6 Cell Line	embryonic stem cell
10	chr2:168553200-168554000	Enhancers	iPS-20b Cell Line	embryonic stem cell
11	chr2:168553200-168555200	Enhancers	iPS-18 Cell Line	embryonic stem cell
12	chr2:168553400-168554200	Enhancers	H9 Cell Line	embryonic stem cell
13	chr2:168553400-168555200	Enhancers	ES-WA7 Cell Line	embryonic stem cell
14	chr2:168553600-168554400	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
15	chr2:168553600-168554400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
16	chr2:168553800-168554000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
17	chr2:168553800-168554000	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
18	chr2:168553800-168554000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
19	chr2:168553800-168554200	Flanking Active TSS	iPS-15b Cell Line	embryonic stem cell
20	chr2:168553800-168554800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
21	chr2:168553800-168555000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
22	chr2:168553800-168555400	Enhancers	ES-I3 Cell Line	embryonic stem cell
23	chr2:168553800-168555400	Enhancers	H1 Cell Line	embryonic stem cell
24	chr2:168554000-168554200	Enhancers	HUES6 Cell Line	embryonic stem cell
25	chr2:168554000-168554600	Flanking Active TSS	HUES64 Cell Line	embryonic stem cell
26	chr2:168554000-168554800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
27	chr2:168554000-168554800	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
28	chr2:168554000-168563400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
29	chr2:168554200-168554400	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
30	chr2:168554200-168555200	Weak transcription	H9 Cell Line	embryonic stem cell
31	chr2:168554200-168555400	Enhancers	iPS-15b Cell Line	embryonic stem cell
32	chr2:168554400-168555400	Enhancers	HUES48 Cell Line	embryonic stem cell
33	chr2:168554400-168555600	Enhancers	HUES6 Cell Line	embryonic stem cell
34	chr2:168554600-168555400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
35	chr2:168554600-168555800	Enhancers	HUES64 Cell Line	embryonic stem cell
36	chr2:168554800-168555400	Enhancers	iPS-20b Cell Line	embryonic stem cell
37	chr2:168554800-168557600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
38	chr2:168555000-168555200	Flanking Bivalent TSS/Enh	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
39	chr2:168555200-168555400	Enhancers	H9 Cell Line	embryonic stem cell
40	chr2:168555200-168555400	Bivalent Enhancer	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
41	chr2:168555400-168559800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
42	chr2:168555400-168572400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
43	chr2:168557600-168557800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
44	chr2:168559600-168560000	Enhancers	Breast Myoepithelial Primary Cells	Breast
45	chr2:168560000-168563400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
46	chr2:168562000-168563600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
47	chr2:168562200-168563800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
48	chr2:168562800-168565600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
49	chr2:168563400-168563600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
50	chr2:168563400-168564600	Enhancers	Breast Myoepithelial Primary Cells	Breast

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