Variant report

Variant	nsv1001771
Chromosome Location	chr1:57837089-58068175
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	chr1:57930387-57930889	HepG2	liver:	n/a	n/a
2	ARID3A	chr1:57865805-57866199	HepG2	liver:	n/a	n/a
3	ATF1	chr1:58063178-58063197	K562	blood:	n/a	n/a
4	ATF1	chr1:57864050-57864128	K562	blood:	n/a	n/a
5	ATF1	chr1:57881351-57881392	K562	blood:	n/a	n/a
6	ATF1	chr1:57980434-57980525	K562	blood:	n/a	n/a
7	BACH1	chr1:57889135-57889439	H1-hESC	embryonic stem cell:	n/a	n/a
8	BACH1	chr1:57889947-57890545	H1-hESC	embryonic stem cell:	n/a	n/a
9	BACH1	chr1:57949785-57950007	H1-hESC	embryonic stem cell:	n/a	n/a
10	BACH1	chr1:57867228-57867785	H1-hESC	embryonic stem cell:	n/a	n/a
11	BACH1	chr1:57887740-57888660	H1-hESC	embryonic stem cell:	n/a	n/a
12	BHLHE40	chr1:57890506-57890512	K562	blood:	n/a	n/a
13	BHLHE40	chr1:57890226-57890640	HepG2	liver:	n/a	n/a
14	BRCA1	chr1:57983395-57984654	Hela-S3	cervix:	n/a	n/a
15	BRCA1	chr1:57876157-57876771	Hela-S3	cervix:	n/a	n/a
16	BRCA1	chr1:57888539-57888585	H1-hESC	embryonic stem cell:	n/a	n/a
17	CEBPB	chr1:57894732-57895088	Hela-S3	cervix:	n/a	n/a
18	CEBPB	chr1:57872184-57872409	H1-hESC	embryonic stem cell:	n/a	chr1:57872289-57872300
19	CEBPB	chr1:57939747-57940125	IMR90	lung:	n/a	n/a
20	CEBPB	chr1:57954905-57955722	IMR90	lung:	n/a	chr1:57955366-57955377 chr1:57955368-57955377 chr1:57954911-57954924 chr1:57955368-57955377 chr1:57955368-57955377 chr1:57954913-57954924 chr1:57955368-57955377 chr1:57954913-57954924 chr1:57955366-57955379
21	CEBPB	chr1:57935693-57936180	Hela-S3	cervix:	n/a	n/a
22	CEBPB	chr1:57919061-57919326	IMR90	lung:	n/a	n/a
23	CEBPB	chr1:57890286-57890652	H1-hESC	embryonic stem cell:	n/a	n/a
24	CEBPB	chr1:57930451-57930832	HepG2	liver:	n/a	n/a
25	CEBPB	chr1:57934843-57935000	H1-hESC	embryonic stem cell:	n/a	n/a
26	CEBPB	chr1:57958843-57958944	K562	blood:	n/a	chr1:57958898-57958909
27	CEBPB	chr1:58058567-58058891	IMR90	lung:	n/a	chr1:58058738-58058749
28	CEBPB	chr1:57919135-57919185	Hela-S3	cervix:	n/a	n/a
29	CEBPB	chr1:57958748-57959054	HepG2	liver:	n/a	chr1:57958898-57958909
30	CEBPB	chr1:57872130-57872472	HepG2	liver:	n/a	chr1:57872289-57872300
31	CEBPB	chr1:57939777-57940102	Hela-S3	cervix:	n/a	n/a
32	CEBPB	chr1:58057454-58057785	HepG2	liver:	n/a	n/a
33	CEBPB	chr1:57930429-57930859	Hela-S3	cervix:	n/a	n/a
34	CEBPB	chr1:58012370-58012559	HepG2	liver:	n/a	chr1:58012453-58012464 chr1:58012499-58012510
35	CEBPB	chr1:58057416-58057954	Hela-S3	cervix:	n/a	n/a
36	CEBPB	chr1:57934275-57935040	IMR90	lung:	n/a	n/a
37	CEBPB	chr1:58058628-58058865	K562	blood:	n/a	chr1:58058738-58058749
38	CEBPB	chr1:58012315-58012513	A549	lung:	n/a	chr1:58012453-58012464 chr1:58012499-58012510
39	CEBPB	chr1:57872155-57872425	K562	blood:	n/a	chr1:57872289-57872300
40	CEBPB	chr1:58017302-58017439	H1-hESC	embryonic stem cell:	n/a	n/a
41	CEBPB	chr1:57850364-57850571	HepG2	liver:	n/a	chr1:57850477-57850488
42	CEBPB	chr1:58058603-58058831	A549	lung:	n/a	chr1:58058738-58058749
43	CEBPB	chr1:57954742-57955820	Hela-S3	cervix:	n/a	chr1:57955366-57955377 chr1:57955368-57955377 chr1:57954911-57954924 chr1:57955368-57955377 chr1:57955368-57955377 chr1:57954913-57954924 chr1:57955368-57955377 chr1:57954913-57954924 chr1:57955366-57955379
44	CEBPB	chr1:57983289-57984755	Hela-S3	cervix:	n/a	n/a
45	CEBPB	chr1:58058579-58058899	HepG2	liver:	n/a	chr1:58058738-58058749
46	CEBPB	chr1:57872187-57872410	A549	lung:	n/a	chr1:57872289-57872300
47	CEBPB	chr1:57849385-57849579	HepG2	liver:	n/a	n/a
48	CEBPB	chr1:57872124-57872469	IMR90	lung:	n/a	chr1:57872289-57872300
49	CEBPB	chr1:57880061-57880317	Hela-S3	cervix:	n/a	n/a
50	CEBPB	chr1:57872161-57872422	Hela-S3	cervix:	n/a	chr1:57872289-57872300

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:57888480-57888530	U87	brain:	n/a
2	chr1:57888480-57888530	U87	brain:	n/a
3	chr1:57888480-57888530	K562	blood:	n/a
4	chr1:58018699-58018749	BJ	skin:	n/a
5	chr1:57889035-57889085	HCM	heart:	n/a
6	chr1:57886427-57886477	NB4	blood:	n/a
7	chr1:57889604-57889654	SK-N-SH	brain:	n/a
8	chr1:57998740-57998790	H1-hESC	embryonic stem cell:	embryo
9	chr1:58063953-58064003	HCPEpiC	choroid plexus:	n/a
10	chr1:57890488-57890538	BE2_C	brain:	n/a
11	chr1:58063953-58064003	ProgFib	skin:	n/a
12	chr1:57887655-57887705	AoSMC	blood vessel:	n/a
13	chr1:57884286-57884336	HRE	kidney:	n/a
14	chr1:57889417-57889467	H1-hESC	embryonic stem cell:	embryo
15	chr1:57892830-57892880	HEEpiC	esophagus:	n/a
16	chr1:57955106-57955156	NT2-D1	testis:	n/a
17	chr1:57884286-57884336	NH-A	brain:	n/a
18	chr1:57889035-57889085	GM19239	blood:	n/a
19	chr1:57890488-57890538	HAEpiC	amniotic membrane:	n/a
20	chr1:57873715-57873765	ECC-1	luminal epithelium:	n/a
21	chr1:57889035-57889085	BJ	skin:	n/a
22	chr1:57890610-57890660	AG10803	skin:	n/a
23	chr1:57888796-57888846	LNCaP	prostate:	n/a
24	chr1:57889417-57889467	SK-N-SH_RA	brain:	n/a
25	chr1:57888796-57888846	RPTEC	kidney:	n/a
26	chr1:57890610-57890660	HCPEpiC	choroid plexus:	n/a
27	chr1:57888480-57888530	HCPEpiC	choroid plexus:	n/a
28	chr1:57890488-57890538	SKMC	muscle:	n/a
29	chr1:57889417-57889467	PrEC	prostate:	n/a
30	chr1:57873715-57873765	HEK293	kidney:	embryo
31	chr1:57889604-57889654	HRPEpiC	eye:	n/a
32	chr1:57888707-57888757	HCM	heart:	n/a
33	chr1:57889417-57889467	HUVEC	blood vessel:	n/a
34	chr1:57890317-57890367	HRPEpiC	eye:	n/a
35	chr1:57890488-57890538	HRE	kidney:	n/a
36	chr1:57890317-57890367	HCT-116	colon:	n/a
37	chr1:57983368-57983418	Caco-2	colon:	n/a
38	chr1:57888343-57888393	BE2_C	brain:	n/a
39	chr1:57998740-57998790	HUVEC	blood vessel:	n/a
40	chr1:57890636-57890686	HCM	heart:	n/a
41	chr1:57888480-57888530	RPTEC	kidney:	n/a
42	chr1:57890636-57890686	HRCEpiC	kidney:	n/a
43	chr1:57888480-57888530	HRE	kidney:	n/a
44	chr1:58018699-58018749	GM06990	blood:	n/a
45	chr1:57888343-57888393	GM12878	blood:	n/a
46	chr1:57890317-57890367	HEEpiC	esophagus:	n/a
47	chr1:58063953-58064003	HCF	heart:	n/a
48	chr1:58063953-58064003	HMEC	breast:	n/a
49	chr1:57888480-57888530	NH-A	brain:	n/a
50	chr1:57983368-57983418	BE2_C	brain:	n/a

No.	Distal block	Cell Line	Cell type
1	chr1:57866069..57868024-chr1:57868935..57871351,2	K562	blood:
2	chr1:57957161..57959249-chr1:57964483..57967237,2	K562	blood:
3	chr1:57866069..57868024-chr1:57868935..57871351,2	K562	blood:
4	chr1:57972252..57973978-chr1:58083473..58085053,2	K562	blood:
5	chr1:57957161..57959249-chr1:57964483..57967237,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C8A-3	chr1:57852248-57852394	ENSG00000227935
2	lnc-C8A-3	chr1:57852562-57853122	ENSG00000227935

Variant related genes	Relation type
DAB1	TF binding region
ENSG00000227935	TF binding region
DAB1	CpG island
ENSG00000227935	CpG island

Extended variants
information (count: 8029 )
Associated
traits (count: 95 )

Variant overlapped rSNPs/rCNVs (count:8029 , 50 per page) page: 1 2 3 4 5 6 7 ... 161

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2216808	chr1:57837089-57837090	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs551203134	chr1:57837144-57837145	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs548335219	chr1:57837145-57837146	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs186546248	chr1:57837195-57837196	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs4433421	chr1:57837271-57837272	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs146036184	chr1:57837312-57837313	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs191191138	chr1:57837327-57837328	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs377523472	chr1:57837331-57837332	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs532528267	chr1:57837337-57837338	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs375184867	chr1:57837341-57837342	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs17423736	chr1:57837349-57837350	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs549944246	chr1:57837432-57837433	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs537240742	chr1:57837435-57837436	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs139792842	chr1:57837450-57837451	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs368044861	chr1:57837492-57837493	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs568552999	chr1:57837586-57837587	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs542179454	chr1:57837639-57837640	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs146213071	chr1:57837662-57837663	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs553431862	chr1:57837671-57837672	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs148437303	chr1:57837699-57837700	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs142396257	chr1:57837732-57837733	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs556204845	chr1:57837740-57837741	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs576238701	chr1:57837743-57837744	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs543656182	chr1:57837745-57837746	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs554124709	chr1:57837757-57837758	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs374452449	chr1:57837777-57837778	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs565466183	chr1:57837805-57837806	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs532556325	chr1:57837866-57837867	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs184483055	chr1:57837957-57837958	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs373786263	chr1:57837990-57837991	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs188226772	chr1:57837991-57837992	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs540758914	chr1:57838096-57838097	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs111695327	chr1:57838113-57838114	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs1981891	chr1:57838140-57838141	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs151291719	chr1:57838187-57838188	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs569460610	chr1:57838191-57838192	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs558582116	chr1:57838200-57838201	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs532074501	chr1:57838236-57838237	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs192797293	chr1:57838261-57838262	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs200900273	chr1:57838262-57838263	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs185087310	chr1:57838314-57838315	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs530151447	chr1:57838326-57838327	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs372069867	chr1:57838327-57838328	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs397727709	chr1:57838335-57838336	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs375139915	chr1:57838340-57838341	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs534113216	chr1:57838397-57838398	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs553464333	chr1:57838404-57838405	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs140562828	chr1:57838411-57838412	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs190013523	chr1:57838435-57838436	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs150049303	chr1:57838462-57838463	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:95)

Disease	PMID	Source
Papillary thyroid carcinoma	21436994	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Colorectal cancer	16272173	CNVD
Wilms tumour	21544195	CNVD
Coronary Disease	20032323	CNVD
Prostate cancer	21965145	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Stargardt''s disease	17277736	CNVD
Neuroblastoma	17897457	CNVD
Uveal melanoma	21693616	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	21484798	CNVD
Non-syndromic sensorineural hearing loss	22290220	CNVD
Liposarcoma	21253554	CNVD
Breast cancer	21264507	CNVD
Acute myeloid leukemia	16864856	CNVD
Astrocytoma	17387387	CNVD
Cancer	21499728	CNVD
Glioblastoma multiforme	17387387	CNVD
Oligodendroglial tumors	17285580	CNVD
Neuroblastoma	17535989	CNVD
Pheochromocytoma	17535989	CNVD
Prostate cancer	16705090	CNVD
Astrocytoma	17934521	CNVD
Colorectal cancer	19359472	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Neuroblastoma	17533364	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Autism	22495311	CNVD
Non-small cell lung cancer	21385341	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Chordoma	21602918	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Melanoma	18172304	CNVD
Multiple myeloma	16461302	CNVD
Melanoma	17363583	CNVD
Cancer	21129771	CNVD
Autosomal dominant nocturnal frontal lobe epilepsy	18472482	CNVD
Hirschsprung''s Disease	21712996	CNVD
Non-small cell lung cancer	20864512	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Thrombocytopenia-absent radius syndrome	21933853	CNVD
Psychiatric disorder	22848183	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	20409316	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Lung cancer	18438408	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17393978	CNVD
Cervical cancer	21062161	CNVD
Cancer	21183584	CNVD
Breast cancer	21785460	CNVD
Breast cancer	21364760	CNVD
Rett syndrome	21593744	CNVD
Meckel-Gruber syndrome	21572526	CNVD
Breast cancer	16620391	CNVD
Multiple myeloma	16616336	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Prostate cancer	16573809	CNVD
Breast cancer	16608533	CNVD
Breast cancer	21509527	CNVD
Myelofibrosis	22110671	CNVD
Developmental delay	19490664	CNVD
Glioblastoma multiforme	22286061	CNVD
Ovarian cancer	21720365	CNVD
Breast cancer	22522925	CNVD
small cell lung cancer	20016488	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Developmental delay	21147756	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:1372 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:57829600-57843400	Weak transcription	Fetal Heart	heart
2	chr1:57830200-57841800	Weak transcription	Fetal Brain Male	brain
3	chr1:57834800-57843200	Weak transcription	H1 Cell Line	embryonic stem cell
4	chr1:57835000-57843200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
5	chr1:57835600-57837200	Enhancers	HUES6 Cell Line	embryonic stem cell
6	chr1:57835600-57837200	Enhancers	iPS-20b Cell Line	embryonic stem cell
7	chr1:57835800-57843000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
8	chr1:57836800-57837400	Enhancers	H9 Cell Line	embryonic stem cell
9	chr1:57837000-57837400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
10	chr1:57837000-57839800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
11	chr1:57837000-57843200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
12	chr1:57837400-57837600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
13	chr1:57837400-57847600	Weak transcription	H9 Cell Line	embryonic stem cell
14	chr1:57837600-57843200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
15	chr1:57838000-57838600	Enhancers	Fetal Lung	lung
16	chr1:57841600-57843200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
17	chr1:57841800-57842200	Enhancers	Fetal Stomach	stomach
18	chr1:57841800-57844000	Enhancers	Fetal Brain Male	brain
19	chr1:57843000-57845200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
20	chr1:57843200-57843600	Enhancers	H1 Cell Line	embryonic stem cell
21	chr1:57843200-57843800	Enhancers	HUES48 Cell Line	embryonic stem cell
22	chr1:57843200-57843800	Enhancers	iPS-18 Cell Line	embryonic stem cell
23	chr1:57843200-57844000	Enhancers	ES-I3 Cell Line	embryonic stem cell
24	chr1:57843200-57844000	Enhancers	HUES6 Cell Line	embryonic stem cell
25	chr1:57843200-57844200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
26	chr1:57843200-57844200	Enhancers	HUES64 Cell Line	embryonic stem cell
27	chr1:57843400-57843600	Enhancers	Fetal Brain Female	brain
28	chr1:57843400-57843800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
29	chr1:57843400-57843800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
30	chr1:57843400-57844000	Enhancers	iPS-20b Cell Line	embryonic stem cell
31	chr1:57843400-57844000	Enhancers	Fetal Heart	heart
32	chr1:57843400-57847600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
33	chr1:57843600-57844000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
34	chr1:57843600-57844200	Weak transcription	Fetal Brain Female	brain
35	chr1:57843600-57847400	Weak transcription	H1 Cell Line	embryonic stem cell
36	chr1:57843800-57847000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
37	chr1:57843800-57847200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
38	chr1:57843800-57847400	Weak transcription	HUES48 Cell Line	embryonic stem cell
39	chr1:57844000-57846600	Weak transcription	Fetal Brain Male	brain
40	chr1:57844000-57846800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
41	chr1:57844000-57847400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
42	chr1:57844000-57847600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
43	chr1:57844000-57847600	Weak transcription	HUES6 Cell Line	embryonic stem cell
44	chr1:57844000-57848000	Weak transcription	Fetal Heart	heart
45	chr1:57844200-57844400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
46	chr1:57844200-57844400	Enhancers	Fetal Brain Female	brain
47	chr1:57844200-57847600	Weak transcription	HUES64 Cell Line	embryonic stem cell
48	chr1:57844400-57844800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
49	chr1:57844400-57847200	Weak transcription	Fetal Brain Female	brain
50	chr1:57844800-57847000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived

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