Variant report

Variant	nsv874352
Chromosome Location	chr2:77980106-78048214
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:106)
CpG islands
(count:61)
Chromatin interactive
region (count:1)
LncRNA
region (count:11)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:106 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr2:78043808-78043996	H1-hESC	embryonic stem cell:	n/a	n/a
2	CEBPB	chr2:77995750-77995921	HepG2	liver:	n/a	chr2:77995852-77995863
3	CEBPB	chr2:78018338-78018524	HepG2	liver:	n/a	chr2:78018470-78018483 chr2:78018453-78018464
4	CEBPB	chr2:77995692-77996037	HepG2	liver:	n/a	chr2:77995852-77995863
5	CEBPB	chr2:78029044-78029185	HepG2	liver:	n/a	chr2:78029126-78029139 chr2:78029127-78029138
6	CHD2	chr2:77981206-77981340	H1-hESC	embryonic stem cell:	n/a	n/a
7	CTCF	chr2:78023560-78023710	BE2_C	brain:	n/a	n/a
8	CTCF	chr2:78035672-78035707	Pancreas_OC	pancreas:	n/a	n/a
9	CTCF	chr2:78023640-78023790	BE2_C	brain:	n/a	n/a
10	CTCF	chr2:78023640-78023790	Caco-2	colon:	n/a	n/a
11	CTCF	chr2:78046932-78046967	GM20000	blood:	n/a	n/a
12	CTCF	chr2:77996793-77996806	GM13976	blood:	n/a	n/a
13	CTCF	chr2:78033617-78033669	Lung_OC	lung:	n/a	n/a
14	CTCF	chr2:77996242-77996290	GM19239	blood:	n/a	n/a
15	CTCF	chr2:77999629-77999640	GM10248	blood:	n/a	n/a
16	CTCF	chr2:78037650-78037693	GM10248	blood:	n/a	n/a
17	CTCF	chr2:78007686-78007720	Lung_OC	lung:	n/a	n/a
18	E2F4	chr2:77992385-77992727	MCF10A-Er-Src	breast:	n/a	n/a
19	E2F4	chr2:78024715-78025098	MCF10A-Er-Src	breast:	n/a	n/a
20	EP300	chr2:78017913-78017915	HepG2	liver:	n/a	n/a
21	EP300	chr2:78027585-78027826	SK-N-SH_RA	brain:	n/a	n/a
22	EP300	chr2:78027202-78027929	SK-N-SH	brain:	n/a	n/a
23	EP300	chr2:78027511-78027934	SK-N-SH_RA	brain:	n/a	n/a
24	EP300	chr2:78016788-78017750	SK-N-SH	brain:	n/a	n/a
25	FOS	chr2:78034937-78035262	MCF10A-Er-Src	breast:	n/a	n/a
26	FOS	chr2:78035048-78035255	MCF10A-Er-Src	breast:	n/a	n/a
27	FOS	chr2:78034997-78035233	MCF10A-Er-Src	breast:	n/a	n/a
28	FOXA1	chr2:77981195-77981403	HepG2	liver:	n/a	n/a
29	FOXA1	chr2:77981177-77981433	HepG2	liver:	n/a	n/a
30	FOXA1	chr2:78005800-78006091	HepG2	liver:	n/a	n/a
31	FOXA1	chr2:77981178-77981433	HepG2	liver:	n/a	n/a
32	FOXA1	chr2:77981184-77981422	HepG2	liver:	n/a	n/a
33	FOXA2	chr2:77980995-77981492	A549	lung:	n/a	n/a
34	FOXA2	chr2:78005851-78006049	HepG2	liver:	n/a	n/a
35	FOXA2	chr2:77981207-77981387	HepG2	liver:	n/a	n/a
36	FOXA2	chr2:77981219-77981525	A549	lung:	n/a	n/a
37	GATA3	chr2:78031867-78032220	T-47D	breast:	n/a	n/a
38	GATA3	chr2:78047726-78047838	SH-SY5Y	brain:	n/a	n/a
39	GATA3	chr2:78027554-78027828	SH-SY5Y	brain:	n/a	n/a
40	GATA3	chr2:78018670-78018890	SH-SY5Y	brain:	n/a	n/a
41	GATA3	chr2:78031017-78031193	SH-SY5Y	brain:	n/a	n/a
42	GATA3	chr2:78031841-78032277	T-47D	breast:	n/a	n/a
43	GATA3	chr2:78046144-78046344	SH-SY5Y	brain:	n/a	n/a
44	IRF1	chr2:77993093-77993169	K562	blood:	n/a	n/a
45	JUND	chr2:78024257-78024495	H1-hESC	embryonic stem cell:	n/a	chr2:78024399-78024407 chr2:78024399-78024406
46	MAFF	chr2:78018707-78018937	HepG2	liver:	n/a	chr2:78018769-78018787
47	MAFK	chr2:78018629-78018930	HepG2	liver:	n/a	chr2:78018770-78018784 chr2:78018771-78018787 chr2:78018772-78018783 chr2:78018771-78018786
48	MAFK	chr2:78043840-78044081	HepG2	liver:	n/a	chr2:78043921-78043930 chr2:78043921-78043931
49	MAFK	chr2:78014326-78014517	H1-hESC	embryonic stem cell:	n/a	n/a
50	MAFK	chr2:78018627-78018907	HepG2	liver:	n/a	chr2:78018770-78018784 chr2:78018771-78018787 chr2:78018772-78018783 chr2:78018771-78018786

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:77981162-77981212	MCF-7	breast:	n/a
2	chr2:77981162-77981212	AG10803	skin:	n/a
3	chr2:77981162-77981212	HCPEpiC	choroid plexus:	n/a
4	chr2:77981162-77981212	GM19239	blood:	n/a
5	chr2:77981162-77981212	GM12878	blood:	n/a
6	chr2:77981162-77981212	Jurkat	blood:	n/a
7	chr2:77981162-77981212	HEEpiC	esophagus:	n/a
8	chr2:77981162-77981212	HAEpiC	amniotic membrane:	n/a
9	chr2:77981162-77981212	HMEC	breast:	n/a
10	chr2:77981162-77981212	NHBE	bronchial:	n/a
11	chr2:77981162-77981212	CMK	blood:	n/a
12	chr2:77981162-77981212	SK-N-MC	brain:	n/a
13	chr2:77981162-77981212	ProgFib	skin:	n/a
14	chr2:77981162-77981212	NT2-D1	testis:	n/a
15	chr2:77981162-77981212	LNCaP	prostate:	n/a
16	chr2:77981162-77981212	H1-hESC	embryonic stem cell:	embryo
17	chr2:77981162-77981212	HepG2	liver:	n/a
18	chr2:77981162-77981212	T-47D	breast:	n/a
19	chr2:77981162-77981212	AG04449	skin:	fetal
20	chr2:77981162-77981212	GM06990	blood:	n/a
21	chr2:77981162-77981212	AG09309	skin:	n/a
22	chr2:77981162-77981212	AoSMC	blood vessel:	n/a
23	chr2:77981162-77981212	HIPEpiC	eye:	n/a
24	chr2:77981162-77981212	SK-N-SH	brain:	n/a
25	chr2:77981162-77981212	NHDF-neo	bronchial:	n/a
26	chr2:77981162-77981212	HCM	heart:	n/a
27	chr2:77981162-77981212	ECC-1	luminal epithelium:	n/a
28	chr2:77981162-77981212	SAEC	small airway:	n/a
29	chr2:77981162-77981212	Caco-2	colon:	n/a
30	chr2:77981162-77981212	NB4	blood:	n/a
31	chr2:77981162-77981212	Hela-S3	cervix:	n/a
32	chr2:77981162-77981212	U87	brain:	n/a
33	chr2:77981162-77981212	HPAEpiC	pulmonary alveolar:	n/a
34	chr2:77981162-77981212	HRPEpiC	eye:	n/a
35	chr2:77981162-77981212	HEK293	kidney:	embryo
36	chr2:77981162-77981212	AG09319	gingival:	n/a
37	chr2:77981162-77981212	HUVEC	blood vessel:	n/a
38	chr2:77981162-77981212	K562	blood:	n/a
39	chr2:77981162-77981212	PANC-1	pancreas:	n/a
40	chr2:77981162-77981212	HCT-116	colon:	n/a
41	chr2:77981162-77981212	ovcar-3	ovarian:	n/a
42	chr2:77981162-77981212	MCF10A-Er-Src	breast:	n/a
43	chr2:77981162-77981212	BJ	skin:	n/a
44	chr2:77981162-77981212	IMR90	lung:	fetal
45	chr2:77981162-77981212	A549	lung:	n/a
46	chr2:77981162-77981212	AG04450	lung:	fetal
47	chr2:77981162-77981212	HL-60	blood:	n/a
48	chr2:77981162-77981212	GM12891	blood:	n/a
49	chr2:77981162-77981212	RPTEC	kidney:	n/a
50	chr2:77981162-77981212	NH-A	brain:	n/a

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr17:56735169..56737848-chr2:78047828..78049670,2	MCF-7	breast:

(count:11 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-REG3G-10	chr2:77998337-77998643	NONHSAT071832
2	lnc-REG3G-10	chr2:77996541-77996727	l_1869_chr2:77996540-77998625_testes
3	lnc-REG3G-10	chr2:77996568-77996727	NONHSAT071832
4	lnc-REG3G-10	chr2:77998337-77998625	l_1869_chr2:77996540-77998625_testes
5	lnc-REG3G-10	chr2:77997871-77998038	NONHSAT071832
6	lnc-REG3G-9	chr2:78019947-78020151	NONHSAT071834
7	lnc-REG3G-10	chr2:77997871-77998038	l_1869_chr2:77996540-77998625_testes
8	lnc-REG3G-9	chr2:78013230-78013238	NONHSAT071833
9	lnc-REG3G-9	chr2:78019858-78020279	NONHSAT071833
10	lnc-REG3G-9	chr2:78014667-78014729	NONHSAT071833
11	lnc-REG3G-9	chr2:78015508-78015637	NONHSAT071833

No data

Variant related genes	Relation type
ENSG00000237077	TF binding region
ENSG00000237077	CpG island
ENSG00000202077	chromatin interactions

Extended variants
information (count: 1530 )
Associated
traits (count: 57 )

Variant overlapped rSNPs/rCNVs (count:1530 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7588183	chr2:77980106-77980107	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs540114151	chr2:77980112-77980113	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs557768189	chr2:77980124-77980125	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs181386291	chr2:77980157-77980158	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs540342763	chr2:77980171-77980172	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs7562077	chr2:77980209-77980210	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs573508827	chr2:77980217-77980218	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs7575968	chr2:77980226-77980227	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs145167613	chr2:77980232-77980233	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs186528538	chr2:77980265-77980266	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs7562185	chr2:77980299-77980300	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs7562190	chr2:77980321-77980322	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs148798007	chr2:77980353-77980354	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs547915561	chr2:77980396-77980397	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs567800675	chr2:77980414-77980415	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs113804440	chr2:77980423-77980424	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs572845270	chr2:77980439-77980440	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs550424093	chr2:77980440-77980441	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs183152813	chr2:77980451-77980452	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs539332740	chr2:77980460-77980461	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs10179533	chr2:77980470-77980471	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs571221867	chr2:77980483-77980484	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs533511092	chr2:77980507-77980508	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs553345821	chr2:77980525-77980526	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs187444174	chr2:77980534-77980535	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs191115995	chr2:77980540-77980541	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs555977037	chr2:77980544-77980545	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs576122525	chr2:77980588-77980589	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs142435312	chr2:77980627-77980628	Active TSS Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs113540204	chr2:77980630-77980631	Active TSS Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs183697845	chr2:77980659-77980660	Active TSS Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs13398413	chr2:77980691-77980692	Active TSS Weak transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs113331515	chr2:77980694-77980695	Active TSS Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs373988358	chr2:77980698-77980699	Active TSS Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs541483732	chr2:77980729-77980730	Active TSS Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs561244577	chr2:77980768-77980769	Active TSS Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs114463202	chr2:77980799-77980800	Active TSS Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs550263220	chr2:77980821-77980822	Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs187895760	chr2:77980831-77980832	Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs572043647	chr2:77980847-77980848	Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs200326374	chr2:77980882-77980883	Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs532548478	chr2:77980885-77980886	Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs192140028	chr2:77980891-77980892	Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs115564527	chr2:77980897-77980898	Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs13398656	chr2:77980913-77980914	Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs184451554	chr2:77980916-77980917	Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs566909587	chr2:77980921-77980922	Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs564328297	chr2:77980931-77980932	Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs187159320	chr2:77980937-77980938	Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs375439279	chr2:77980941-77980942	Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:57)

Disease	PMID	Source
Chronic lymphocytic leukemia	21546498	CNVD
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17387387	CNVD
Neuroblastoma	17533364	CNVD
Neuroblastoma	18923191	CNVD
Endometrial cancer	22040021	CNVD
Adrenal tumor	17535989	CNVD
Breast cancer	21264507	CNVD
Basal cell lymphoma	17053054	CNVD
Medulloblastoma	17522785	CNVD
Cancer	23418310	CNVD
Medulloblastoma	21979893	CNVD
Breast cancer	17603634	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Ependymoma	16718352	CNVD
Prostate cancer	18632612	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Follicular lymphoma	20505157	CNVD
Autism	17483303	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Medulloblastoma	20607354	CNVD
Autism	22495311	CNVD
Autism	18522746	CNVD
Neurodevelopmental disorder	22521361	CNVD
Lung cancer	18438408	CNVD
Melanoma	18172304	CNVD
Cancer	16751803	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Seminomas	18059402	CNVD
Testicular germ cell tumor	18059402	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Renal cell carcinoma	18765545	CNVD
Myxofibrosarcoma	16751306	CNVD
small cell lung cancer	20016488	CNVD
Acute myeloid leukemia	21251322	CNVD
Mental retardation	17124404	CNVD
Basal cell lymphoma	19029149	CNVD
Diffuse large b-cell lymphoma	19029149	CNVD
Cancer	17440070	CNVD
Myelofibrosis	22110671	CNVD
Attention deficit hyperactivity disorder	21324949	CNVD
Breast cancer	16272173	CNVD
Epilepsy	22083797	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Schizophrenia	23813976	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:73 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:77975200-77980800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr2:77980000-77980800	Weak transcription	H9 Cell Line	embryonic stem cell
3	chr2:77980400-77980600	Enhancers	HUES64 Cell Line	embryonic stem cell
4	chr2:77980600-77980800	Flanking Active TSS	HUES64 Cell Line	embryonic stem cell
5	chr2:77980600-77981400	Active TSS	ES-I3 Cell Line	embryonic stem cell
6	chr2:77980600-77981400	Active TSS	HUES48 Cell Line	embryonic stem cell
7	chr2:77980600-77981400	Active TSS	iPS-15b Cell Line	embryonic stem cell
8	chr2:77980600-77981400	Active TSS	iPS-18 Cell Line	embryonic stem cell
9	chr2:77980600-77981400	Active TSS	iPS-20b Cell Line	embryonic stem cell
10	chr2:77980600-77981600	Active TSS	H1 Cell Line	embryonic stem cell
11	chr2:77980600-77981600	Active TSS	HUES6 Cell Line	embryonic stem cell
12	chr2:77980800-77981200	Active TSS	ES-WA7 Cell Line	embryonic stem cell
13	chr2:77980800-77981400	Active TSS	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
14	chr2:77980800-77981400	Active TSS	H9 Cell Line	embryonic stem cell
15	chr2:77980800-77981400	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
16	chr2:77980800-77981400	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
17	chr2:77980800-77981600	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
18	chr2:77980800-77981600	Active TSS	HUES64 Cell Line	embryonic stem cell
19	chr2:77980800-77981600	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
20	chr2:77994400-77994800	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
21	chr2:77994600-77995000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
22	chr2:77994600-77996200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
23	chr2:77995000-77995200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
24	chr2:77995000-77997400	Weak transcription	Right Atrium	heart
25	chr2:77995200-77996200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
26	chr2:77996200-77996400	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
27	chr2:77996200-77996400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
28	chr2:77996400-77999800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
29	chr2:77999800-78000400	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
30	chr2:78013600-78014200	Enhancers	HUES48 Cell Line	embryonic stem cell
31	chr2:78013800-78014600	Enhancers	HUES64 Cell Line	embryonic stem cell
32	chr2:78014000-78014400	Enhancers	iPS-15b Cell Line	embryonic stem cell
33	chr2:78017800-78018000	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
34	chr2:78018000-78021200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
35	chr2:78023800-78024600	Enhancers	iPS-15b Cell Line	embryonic stem cell
36	chr2:78023800-78025000	Enhancers	HUES48 Cell Line	embryonic stem cell
37	chr2:78023800-78025200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
38	chr2:78024200-78024600	Enhancers	HUES64 Cell Line	embryonic stem cell
39	chr2:78024200-78024800	Enhancers	iPS-18 Cell Line	embryonic stem cell
40	chr2:78024400-78025200	Enhancers	H9 Cell Line	embryonic stem cell
41	chr2:78031000-78031200	Enhancers	Breast Myoepithelial Primary Cells	Breast
42	chr2:78031400-78032000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
43	chr2:78031600-78031800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
44	chr2:78031800-78033000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
45	chr2:78032000-78033000	Enhancers	Breast Myoepithelial Primary Cells	Breast
46	chr2:78032800-78033000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
47	chr2:78033000-78033400	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
48	chr2:78033000-78036000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
49	chr2:78033800-78036000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
50	chr2:78034800-78035000	Enhancers	H9 Cell Line	embryonic stem cell

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links