Variant report

Variant	nsv582260
Chromosome Location	chr2:77936295-78027298
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:163)
CpG islands
(count:184)
Chromatin interactive
region (count:0)
LncRNA
region (count:12)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:163 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CEBPB	chr2:78018338-78018524	HepG2	liver:	n/a	chr2:78018470-78018483 chr2:78018453-78018464
2	CEBPB	chr2:77946096-77946340	A549	lung:	n/a	chr2:77946226-77946239 chr2:77946226-77946237 chr2:77946226-77946239
3	CEBPB	chr2:77955576-77955730	HepG2	liver:	n/a	chr2:77955582-77955593
4	CEBPB	chr2:77995750-77995921	HepG2	liver:	n/a	chr2:77995852-77995863
5	CEBPB	chr2:77946087-77946386	HepG2	liver:	n/a	chr2:77946226-77946239 chr2:77946226-77946237 chr2:77946226-77946239
6	CEBPB	chr2:77995692-77996037	HepG2	liver:	n/a	chr2:77995852-77995863
7	CEBPB	chr2:77950062-77950237	HepG2	liver:	n/a	chr2:77950092-77950103
8	CHD2	chr2:77981206-77981340	H1-hESC	embryonic stem cell:	n/a	n/a
9	CTCF	chr2:78023560-78023710	BE2_C	brain:	n/a	n/a
10	CTCF	chr2:77962940-77963090	RPTEC	kidney:	n/a	n/a
11	CTCF	chr2:77962880-77963030	HepG2	liver:	n/a	n/a
12	CTCF	chr2:77962920-77963070	RPTEC	kidney:	n/a	n/a
13	CTCF	chr2:77962900-77963050	Caco-2	colon:	n/a	n/a
14	CTCF	chr2:78023640-78023790	Caco-2	colon:	n/a	n/a
15	CTCF	chr2:78023640-78023790	BE2_C	brain:	n/a	n/a
16	CTCF	chr2:77963643-77963782	LNCaP	prostate:	n/a	chr2:77963682-77963703
17	CTCF	chr2:77962937-77962995	LNCaP	prostate:	n/a	n/a
18	CTCF	chr2:77962935-77963023	MCF-7	breast:	n/a	n/a
19	CTCF	chr2:77999629-77999640	GM10248	blood:	n/a	n/a
20	CTCF	chr2:77962981-77963000	Hela-S3	cervix:	n/a	n/a
21	CTCF	chr2:78007686-78007720	Lung_OC	lung:	n/a	n/a
22	CTCF	chr2:77962940-77963090	HepG2	liver:	n/a	n/a
23	CTCF	chr2:77962972-77963030	LNCaP	prostate:	n/a	n/a
24	CTCF	chr2:77996793-77996806	GM13976	blood:	n/a	n/a
25	CTCF	chr2:77996242-77996290	GM19239	blood:	n/a	n/a
26	E2F4	chr2:77992385-77992727	MCF10A-Er-Src	breast:	n/a	n/a
27	E2F4	chr2:78024715-78025098	MCF10A-Er-Src	breast:	n/a	n/a
28	E2F4	chr2:77963026-77963152	MCF10A-Er-Src	breast:	n/a	n/a
29	EP300	chr2:78027202-78027929	SK-N-SH	brain:	n/a	n/a
30	EP300	chr2:78017913-78017915	HepG2	liver:	n/a	n/a
31	EP300	chr2:78016788-78017750	SK-N-SH	brain:	n/a	n/a
32	EP300	chr2:77973860-77974387	HepG2	liver:	n/a	n/a
33	EP300	chr2:77973960-77974183	SK-N-SH_RA	brain:	n/a	n/a
34	EP300	chr2:77973914-77974265	SK-N-SH_RA	brain:	n/a	n/a
35	FOSL2	chr2:77973960-77974261	HepG2	liver:	n/a	n/a
36	FOXA1	chr2:77948649-77949099	HepG2	liver:	n/a	n/a
37	FOXA1	chr2:77981184-77981422	HepG2	liver:	n/a	n/a
38	FOXA1	chr2:77981195-77981403	HepG2	liver:	n/a	n/a
39	FOXA1	chr2:77973887-77974238	HepG2	liver:	n/a	n/a
40	FOXA1	chr2:77981178-77981433	HepG2	liver:	n/a	n/a
41	FOXA1	chr2:78005800-78006091	HepG2	liver:	n/a	n/a
42	FOXA1	chr2:77973890-77974198	HepG2	liver:	n/a	n/a
43	FOXA1	chr2:77973855-77974283	HepG2	liver:	n/a	n/a
44	FOXA1	chr2:77948667-77948988	HepG2	liver:	n/a	n/a
45	FOXA1	chr2:77981177-77981433	HepG2	liver:	n/a	n/a
46	FOXA1	chr2:77949256-77949458	HepG2	liver:	n/a	n/a
47	FOXA1	chr2:77973907-77974369	HepG2	liver:	n/a	n/a
48	FOXA1	chr2:77948617-77948997	HepG2	liver:	n/a	n/a
49	FOXA2	chr2:77981219-77981525	A549	lung:	n/a	n/a
50	FOXA2	chr2:77973872-77974468	HepG2	liver:	n/a	n/a

(count:184 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:77981162-77981212	Hepatocyte	liver:	n/a
2	chr2:77981162-77981212	Hepatocyte	liver:	n/a
3	chr2:77962212-77962262	Hela-S3	cervix:	n/a
4	chr2:77962212-77962262	LNCaP	prostate:	n/a
5	chr2:77981162-77981212	IMR90	lung:	fetal
6	chr2:77981162-77981212	SK-N-SH	brain:	n/a
7	chr2:77962212-77962262	HRE	kidney:	n/a
8	chr2:77981162-77981212	GM12891	blood:	n/a
9	chr2:77981162-77981212	H1-hESC	embryonic stem cell:	embryo
10	chr2:77981162-77981212	HEK293	kidney:	embryo
11	chr2:77961984-77962034	Jurkat	blood:	n/a
12	chr2:77981162-77981212	PrEC	prostate:	n/a
13	chr2:77961984-77962034	SK-N-SH	brain:	n/a
14	chr2:77962212-77962262	AG10803	skin:	n/a
15	chr2:77981162-77981212	GM12892	blood:	n/a
16	chr2:77962212-77962262	ECC-1	luminal epithelium:	n/a
17	chr2:77962212-77962262	HepG2	liver:	n/a
18	chr2:77962212-77962262	NB4	blood:	n/a
19	chr2:77962212-77962262	T-47D	breast:	n/a
20	chr2:77962212-77962262	GM12892	blood:	n/a
21	chr2:77961984-77962034	GM12892	blood:	n/a
22	chr2:77961984-77962034	HEK293	kidney:	embryo
23	chr2:77962212-77962262	NH-A	brain:	n/a
24	chr2:77961984-77962034	MCF-7	breast:	n/a
25	chr2:77981162-77981212	HL-60	blood:	n/a
26	chr2:77981162-77981212	HIPEpiC	eye:	n/a
27	chr2:77962212-77962262	AG09309	skin:	n/a
28	chr2:77981162-77981212	MCF-7	breast:	n/a
29	chr2:77962212-77962262	IMR90	lung:	fetal
30	chr2:77962212-77962262	SK-N-SH_RA	brain:	n/a
31	chr2:77962212-77962262	SK-N-SH	brain:	n/a
32	chr2:77961984-77962034	HL-60	blood:	n/a
33	chr2:77962212-77962262	PrEC	prostate:	n/a
34	chr2:77962212-77962262	SKMC	muscle:	n/a
35	chr2:77981162-77981212	NT2-D1	testis:	n/a
36	chr2:77961984-77962034	PrEC	prostate:	n/a
37	chr2:77961984-77962034	HMEC	breast:	n/a
38	chr2:77962212-77962262	K562	blood:	n/a
39	chr2:77962212-77962262	HAEpiC	amniotic membrane:	n/a
40	chr2:77962212-77962262	HCT-116	colon:	n/a
41	chr2:77961984-77962034	HCM	heart:	n/a
42	chr2:77981162-77981212	HMEC	breast:	n/a
43	chr2:77961984-77962034	HCPEpiC	choroid plexus:	n/a
44	chr2:77961984-77962034	NT2-D1	testis:	n/a
45	chr2:77961984-77962034	Hepatocyte	liver:	n/a
46	chr2:77961984-77962034	SKMC	muscle:	n/a
47	chr2:77962212-77962262	HUVEC	blood vessel:	n/a
48	chr2:77961984-77962034	GM06990	blood:	n/a
49	chr2:77961984-77962034	NHBE	bronchial:	n/a
50	chr2:77961984-77962034	HRCEpiC	kidney:	n/a

No data

(count:12 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-REG3G-10	chr2:77996568-77996727	NONHSAT071832
2	lnc-REG3G-10	chr2:77996541-77996727	l_1869_chr2:77996540-77998625_testes
3	lnc-REG3G-10	chr2:77997871-77998038	l_1869_chr2:77996540-77998625_testes
4	lnc-REG3G-9	chr2:78019858-78020279	NONHSAT071833
5	lnc-LRRTM4-3	chr2:77970822-77970948	NR_110288
6	lnc-REG3G-9	chr2:78013230-78013238	NONHSAT071833
7	lnc-REG3G-10	chr2:77998337-77998643	NONHSAT071832
8	lnc-REG3G-9	chr2:78015508-78015637	NONHSAT071833
9	lnc-REG3G-10	chr2:77998337-77998625	l_1869_chr2:77996540-77998625_testes
10	lnc-REG3G-10	chr2:77997871-77998038	NONHSAT071832
11	lnc-REG3G-9	chr2:78019947-78020151	NONHSAT071834
12	lnc-REG3G-9	chr2:78014667-78014729	NONHSAT071833

No data

Variant related genes	Relation type
ENSG00000237077	TF binding region
ENSG00000237077	CpG island

Extended variants
information (count: 1593 )
Associated
traits (count: 58 )

Variant overlapped rSNPs/rCNVs (count:1593 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs111968174	chr2:77940202-77940203	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs116665888	chr2:77940209-77940210	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs578158189	chr2:77940211-77940212	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs729756	chr2:77940273-77940274	Enhancers	n/a	n/a	Overlapped CNVs	mRNA abundance
5	rs75877485	chr2:77940423-77940424	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs555375492	chr2:77940431-77940432	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs141216303	chr2:77940535-77940536	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs570375707	chr2:77940567-77940568	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs541439354	chr2:77940601-77940602	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs190240293	chr2:77940604-77940605	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs12624137	chr2:77940612-77940613	Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs182470383	chr2:77940633-77940634	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs564013875	chr2:77940655-77940656	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs542445468	chr2:77940663-77940664	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs6720640	chr2:77940668-77940669	Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs566797561	chr2:77940699-77940700	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs142479138	chr2:77940715-77940716	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs185855799	chr2:77940716-77940717	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs370547981	chr2:77940729-77940730	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs151322426	chr2:77940731-77940732	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs191153760	chr2:77940735-77940736	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs532597238	chr2:77940747-77940748	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs181227932	chr2:77940751-77940752	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs556761374	chr2:77940771-77940772	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs75812473	chr2:77940788-77940789	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs574003642	chr2:77940797-77940798	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs575347500	chr2:77940803-77940804	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs542864319	chr2:77940817-77940818	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs562837086	chr2:77940866-77940867	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs575234613	chr2:77940891-77940892	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs4420728	chr2:77940992-77940993	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs543844156	chr2:77941009-77941010	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs568225631	chr2:77941041-77941042	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs564236692	chr2:77941080-77941081	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs537830720	chr2:77941110-77941111	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs535611157	chr2:77941151-77941152	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs140566025	chr2:77941180-77941181	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs554204942	chr2:77941215-77941216	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs560351762	chr2:77941246-77941247	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs17014427	chr2:77941275-77941276	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs185883535	chr2:77941298-77941299	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs374664926	chr2:77941307-77941308	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs150462570	chr2:77941389-77941390	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs72928055	chr2:77941391-77941392	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs551457799	chr2:77941437-77941438	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs571727802	chr2:77941503-77941504	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs533997285	chr2:77941514-77941515	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs553945557	chr2:77941538-77941539	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs142691555	chr2:77941561-77941562	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs142079097	chr2:77941597-77941598	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:58)

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
Lung cancer	18438408	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
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
Non-syndromic sensorineural hearing loss	18451855	CNVD
Schizophrenia	23813976	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:59 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:77940200-77941600	Enhancers	HUES64 Cell Line	embryonic stem cell
2	chr2:77940400-77940600	Enhancers	HUES48 Cell Line	embryonic stem cell
3	chr2:77940400-77941000	Enhancers	HUES6 Cell Line	embryonic stem cell
4	chr2:77940400-77941400	Enhancers	ES-I3 Cell Line	embryonic stem cell
5	chr2:77940400-77941400	Enhancers	iPS-15b Cell Line	embryonic stem cell
6	chr2:77940600-77941000	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
7	chr2:77940600-77941000	Enhancers	iPS-20b Cell Line	embryonic stem cell
8	chr2:77940800-77941400	Enhancers	ES-WA7 Cell Line	embryonic stem cell
9	chr2:77940800-77941400	Enhancers	iPS-18 Cell Line	embryonic stem cell
10	chr2:77941000-77941400	Enhancers	HUES48 Cell Line	embryonic stem cell
11	chr2:77948600-77949400	Enhancers	HepG2	liver
12	chr2:77954200-77961800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
13	chr2:77961800-77962400	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
14	chr2:77974000-77975200	Enhancers	HepG2	liver
15	chr2:77975000-77975200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
16	chr2:77975200-77975600	Weak transcription	HepG2	liver
17	chr2:77975200-77980800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
18	chr2:77975600-77976000	Enhancers	HepG2	liver
19	chr2:77977200-77977600	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
20	chr2:77979400-77980000	Enhancers	H9 Cell Line	embryonic stem cell
21	chr2:77980000-77980800	Weak transcription	H9 Cell Line	embryonic stem cell
22	chr2:77980400-77980600	Enhancers	HUES64 Cell Line	embryonic stem cell
23	chr2:77980600-77980800	Flanking Active TSS	HUES64 Cell Line	embryonic stem cell
24	chr2:77980600-77981400	Active TSS	ES-I3 Cell Line	embryonic stem cell
25	chr2:77980600-77981400	Active TSS	HUES48 Cell Line	embryonic stem cell
26	chr2:77980600-77981400	Active TSS	iPS-15b Cell Line	embryonic stem cell
27	chr2:77980600-77981400	Active TSS	iPS-18 Cell Line	embryonic stem cell
28	chr2:77980600-77981400	Active TSS	iPS-20b Cell Line	embryonic stem cell
29	chr2:77980600-77981600	Active TSS	H1 Cell Line	embryonic stem cell
30	chr2:77980600-77981600	Active TSS	HUES6 Cell Line	embryonic stem cell
31	chr2:77980800-77981200	Active TSS	ES-WA7 Cell Line	embryonic stem cell
32	chr2:77980800-77981400	Active TSS	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
33	chr2:77980800-77981400	Active TSS	H9 Cell Line	embryonic stem cell
34	chr2:77980800-77981400	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
35	chr2:77980800-77981400	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
36	chr2:77980800-77981600	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
37	chr2:77980800-77981600	Active TSS	HUES64 Cell Line	embryonic stem cell
38	chr2:77980800-77981600	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
39	chr2:77994400-77994800	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
40	chr2:77994600-77995000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
41	chr2:77994600-77996200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
42	chr2:77995000-77995200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
43	chr2:77995000-77997400	Weak transcription	Right Atrium	heart
44	chr2:77995200-77996200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
45	chr2:77996200-77996400	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
46	chr2:77996200-77996400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
47	chr2:77996400-77999800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
48	chr2:77999800-78000400	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
49	chr2:78013600-78014200	Enhancers	HUES48 Cell Line	embryonic stem cell
50	chr2:78013800-78014600	Enhancers	HUES64 Cell Line	embryonic stem cell

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