Variant report

Variant	nsv594117
Chromosome Location	chr4:46635167-46846042
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:511)
CpG islands
(count:427)
Chromatin interactive
region (count:7)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:511 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:46839805-46840062	HepG2	liver:	n/a	n/a
2	BRCA1	chr4:46813754-46813779	GM12878	blood:	n/a	n/a
3	BRCA1	chr4:46757106-46757116	GM12878	blood:	n/a	n/a
4	CCNT2	chr4:46711119-46711313	K562	blood:	n/a	n/a
5	CEBPB	chr4:46837117-46837445	HepG2	liver:	n/a	chr4:46837309-46837320
6	CEBPB	chr4:46770005-46770242	K562	blood:	n/a	n/a
7	CEBPB	chr4:46769999-46770252	H1-hESC	embryonic stem cell:	n/a	n/a
8	CEBPB	chr4:46670599-46670937	HepG2	liver:	n/a	chr4:46670759-46670772 chr4:46670759-46670772 chr4:46670760-46670771
9	CEBPB	chr4:46670638-46670838	Hela-S3	cervix:	n/a	chr4:46670759-46670772 chr4:46670759-46670772 chr4:46670760-46670771
10	CEBPB	chr4:46839806-46839908	HepG2	liver:	n/a	n/a
11	CEBPB	chr4:46670606-46670927	A549	lung:	n/a	chr4:46670759-46670772 chr4:46670759-46670772 chr4:46670760-46670771
12	CEBPB	chr4:46650166-46650506	H1-hESC	embryonic stem cell:	n/a	n/a
13	CEBPB	chr4:46837106-46837429	A549	lung:	n/a	chr4:46837309-46837320
14	CEBPB	chr4:46769948-46770292	HepG2	liver:	n/a	n/a
15	CEBPB	chr4:46770004-46770192	A549	lung:	n/a	n/a
16	CEBPB	chr4:46787591-46787693	HepG2	liver:	n/a	chr4:46787614-46787627
17	CEBPB	chr4:46670619-46670896	H1-hESC	embryonic stem cell:	n/a	chr4:46670759-46670772 chr4:46670759-46670772 chr4:46670760-46670771
18	CEBPB	chr4:46769957-46770292	IMR90	lung:	n/a	n/a
19	CHD2	chr4:46678461-46678551	H1-hESC	embryonic stem cell:	n/a	n/a
20	CTCF	chr4:46698861-46698902	GM20000	blood:	n/a	n/a
21	CTCF	chr4:46650300-46650450	GM12864	blood:	n/a	n/a
22	CTCF	chr4:46650251-46650465	K562	blood:	n/a	n/a
23	CTCF	chr4:46650197-46650496	GM19238	blood:	n/a	n/a
24	CTCF	chr4:46650145-46650554	IMR90	lung:	n/a	n/a
25	CTCF	chr4:46650280-46650430	K562	blood:	n/a	n/a
26	CTCF	chr4:46650344-46650393	Spleen_OC	spleen:	n/a	n/a
27	CTCF	chr4:46650149-46650557	GM12878	blood:	n/a	n/a
28	CTCF	chr4:46650108-46650461	MCF-7	breast:	n/a	n/a
29	CTCF	chr4:46650220-46650370	A549	lung:	n/a	n/a
30	CTCF	chr4:46717540-46717690	HEK293	kidney:	n/a	n/a
31	CTCF	chr4:46778260-46778410	Caco-2	colon:	n/a	chr4:46778362-46778380 chr4:46778364-46778385
32	CTCF	chr4:46650260-46650410	HCPEpiC	choroid plexus:	n/a	n/a
33	CTCF	chr4:46650300-46650450	GM12865	blood:	n/a	n/a
34	CTCF	chr4:46650300-46650450	GM06990	blood:	n/a	n/a
35	CTCF	chr4:46650280-46650430	AG04450	lung:	n/a	n/a
36	CTCF	chr4:46650280-46650430	GM12869	blood:	n/a	n/a
37	CTCF	chr4:46650280-46650430	HFF	foreskin:	n/a	n/a
38	CTCF	chr4:46650240-46650390	HCM	heart:	n/a	n/a
39	CTCF	chr4:46650320-46650470	SAEC	small airway:	n/a	n/a
40	CTCF	chr4:46650280-46650430	GM12872	blood:	n/a	n/a
41	CTCF	chr4:46717600-46717750	HepG2	liver:	n/a	n/a
42	CTCF	chr4:46650280-46650430	HMEC	breast:	n/a	n/a
43	CTCF	chr4:46650219-46650496	LNCaP	prostate:	n/a	n/a
44	CTCF	chr4:46650260-46650410	GM06990	blood:	n/a	n/a
45	CTCF	chr4:46650240-46650390	RPTEC	kidney:	n/a	n/a
46	CTCF	chr4:46650206-46650494	NHEK	skin:	n/a	n/a
47	CTCF	chr4:46778323-46778436	LNCaP	prostate:	n/a	chr4:46778362-46778380 chr4:46778364-46778385
48	CTCF	chr4:46650280-46650430	HA-sp	spinal cord:	n/a	n/a
49	CTCF	chr4:46650300-46650450	HAc	cerebellar:	n/a	n/a
50	CTCF	chr4:46650280-46650430	GM12864	blood:	n/a	n/a

(count:427 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:46783754-46783804	GM06990	blood:	n/a
2	chr4:46806296-46806346	AG09319	gingival:	n/a
3	chr4:46738197-46738247	HRPEpiC	eye:	n/a
4	chr4:46726121-46726171	BE2_C	brain:	n/a
5	chr4:46806296-46806346	LNCaP	prostate:	n/a
6	chr4:46806296-46806346	GM12891	blood:	n/a
7	chr4:46738197-46738247	PrEC	prostate:	n/a
8	chr4:46737408-46737458	HEK293	kidney:	embryo
9	chr4:46725938-46725988	HCF	heart:	n/a
10	chr4:46783754-46783804	HCM	heart:	n/a
11	chr4:46726121-46726171	NHBE	bronchial:	n/a
12	chr4:46725938-46725988	A549	lung:	n/a
13	chr4:46738197-46738247	ECC-1	luminal epithelium:	n/a
14	chr4:46738197-46738247	GM12878	blood:	n/a
15	chr4:46806296-46806346	K562	blood:	n/a
16	chr4:46806296-46806346	HAEpiC	amniotic membrane:	n/a
17	chr4:46738197-46738247	HEK293	kidney:	embryo
18	chr4:46726121-46726171	Jurkat	blood:	n/a
19	chr4:46726121-46726171	AG10803	skin:	n/a
20	chr4:46738197-46738247	GM12892	blood:	n/a
21	chr4:46737312-46737362	NH-A	brain:	n/a
22	chr4:46737408-46737458	PANC-1	pancreas:	n/a
23	chr4:46737408-46737458	U87	brain:	n/a
24	chr4:46738197-46738247	GM06990	blood:	n/a
25	chr4:46806296-46806346	AoSMC	blood vessel:	n/a
26	chr4:46738197-46738247	Hela-S3	cervix:	n/a
27	chr4:46738197-46738247	HL-60	blood:	n/a
28	chr4:46725938-46725988	AoSMC	blood vessel:	n/a
29	chr4:46737408-46737458	HRPEpiC	eye:	n/a
30	chr4:46783754-46783804	GM12891	blood:	n/a
31	chr4:46725938-46725988	U87	brain:	n/a
32	chr4:46806296-46806346	Jurkat	blood:	n/a
33	chr4:46737312-46737362	HPAEpiC	pulmonary alveolar:	n/a
34	chr4:46806296-46806346	HEK293	kidney:	embryo
35	chr4:46726121-46726171	PrEC	prostate:	n/a
36	chr4:46806296-46806346	Hepatocyte	liver:	n/a
37	chr4:46738197-46738247	AG09319	gingival:	n/a
38	chr4:46783754-46783804	HEK293	kidney:	embryo
39	chr4:46806296-46806346	HNPCEpiC	eye:	n/a
40	chr4:46783754-46783804	HepG2	liver:	n/a
41	chr4:46725938-46725988	H1-hESC	embryonic stem cell:	embryo
42	chr4:46726121-46726171	HIPEpiC	eye:	n/a
43	chr4:46726121-46726171	GM12878	blood:	n/a
44	chr4:46738197-46738247	Caco-2	colon:	n/a
45	chr4:46726121-46726171	MCF-7	breast:	n/a
46	chr4:46737312-46737362	HRE	kidney:	n/a
47	chr4:46737408-46737458	LNCaP	prostate:	n/a
48	chr4:46783754-46783804	Jurkat	blood:	n/a
49	chr4:46726121-46726171	NT2-D1	testis:	n/a
50	chr4:46726121-46726171	HRE	kidney:	n/a

(count:7 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:46745874..46747839-chr4:46749414..46751916,2	MCF-7	breast:
2	chr4:46745874..46747839-chr4:46749414..46751916,2	MCF-7	breast:
3	chr4:46733082..46735429-chr4:46735919..46738940,3	K562	blood:
4	chr4:46733082..46735429-chr4:46735919..46738940,3	K562	blood:
5	chr4:46809130..46811667-chr4:46812436..46814342,2	K562	blood:
6	chr4:46845685..46846601-chr4:47385587..47386221,2	MCF-7	breast:
7	chr4:46809130..46811667-chr4:46812436..46814342,2	K562	blood:

No data

Variant related genes	Relation type
RAC1P2	TF binding region
RAC1P2	CpG island

Extended variants
information (count: 1918 )
Associated
traits (count: 66 )

Variant overlapped rSNPs/rCNVs (count:1918 , 50 per page) page: 1 2 3 4 5 6 7 ... 39

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs541099830	chr4:46649602-46649603	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs76874559	chr4:46649624-46649625	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs559537540	chr4:46649688-46649689	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs114965614	chr4:46649702-46649703	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs551539335	chr4:46649752-46649753	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs115741010	chr4:46649826-46649827	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs377341342	chr4:46649904-46649905	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs548969450	chr4:46649916-46649917	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs77149533	chr4:46649925-46649926	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs189492630	chr4:46649959-46649960	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs139841420	chr4:46649961-46649962	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs182240404	chr4:46649993-46649994	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs28444653	chr4:46650040-46650041	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs530649453	chr4:46650087-46650088	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs185248212	chr4:46650115-46650116	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs190342838	chr4:46650161-46650162	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs542511134	chr4:46650166-46650167	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs555755285	chr4:46650198-46650199	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs531837379	chr4:46655600-46655601	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
20	rs543525203	chr4:46655627-46655628	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
21	rs62302753	chr4:46655631-46655632	ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs557302062	chr4:46655632-46655633	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
23	rs73244162	chr4:46655667-46655668	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
24	rs547581880	chr4:46655675-46655676	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
25	rs566071748	chr4:46655714-46655715	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
26	rs4695166	chr4:46655734-46655735	ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs575563198	chr4:46655751-46655752	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
28	rs369793312	chr4:46655872-46655873	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
29	rs536274769	chr4:46655880-46655881	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
30	rs554515756	chr4:46655889-46655890	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
31	rs572886810	chr4:46655890-46655891	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
32	rs555532675	chr4:46655903-46655904	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
33	rs139345610	chr4:46655925-46655926	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
34	rs534864651	chr4:46655941-46655942	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
35	rs553195976	chr4:46655969-46655970	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
36	rs540301962	chr4:46655970-46655971	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
37	rs544929630	chr4:46655974-46655975	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
38	rs111271977	chr4:46657415-46657416	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs538839588	chr4:46657437-46657438	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs569005131	chr4:46657459-46657460	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs372952647	chr4:46657505-46657506	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs570736222	chr4:46657543-46657544	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs540092919	chr4:46657570-46657571	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs529950645	chr4:46657610-46657611	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs547014589	chr4:46657614-46657615	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs548109955	chr4:46657663-46657664	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs550766684	chr4:46657703-46657704	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs566406527	chr4:46657736-46657737	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs145966056	chr4:46657755-46657756	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs386674219	chr4:46657829-46657830	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:66)

Disease	PMID	Source
Colorectal cancer	19359472	CNVD
Neuroblastoma	17533364	CNVD
Oral squamous cell carcinoma	17134496	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Cancer	21637783	CNVD
Melanoma	21693616	CNVD
Squamous cell cancer	21044232	CNVD
Colorectal cancer	20709793	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Non-small cell lung cancer	21044232	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	17387387	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Cervical cancer	21062161	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Glioblastoma multiforme	21080181	CNVD
Chordoma	21602918	CNVD
HIV/AIDS	22032296	CNVD
Medulloblastoma	21979893	CNVD
Neuroblastoma	18923191	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	21858162	CNVD
small cell lung cancer	20016488	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Gastric cancer	21586687	CNVD
lymphocytic leukemia	21291569	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	16608533	CNVD
Non-small cell lung cancer	21829676	CNVD
Melanoma	22183965	CNVD
Olfactory neuroblastoma	18408657	CNVD
Cancer	22183965	CNVD
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Renal cell carcinoma	18194544	CNVD
Breast cancer	17603634	CNVD
Glioblastoma multiforme	21922591	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Multiple myeloma	16616336	CNVD
Parkinson disease	21956041	CNVD
Mental retardation	20522426	CNVD
delayed speech	20522426	CNVD
growth disorder	20522426	CNVD
Hepatocellular carcinoma	16750200	CNVD
Myxofibrosarcoma	16751306	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Acute myeloid leukemia	20729466	CNVD
Cancer	20164919	CNVD
Renal cell carcinoma	18765545	CNVD
Gastric cancer	16891809	CNVD
Myelofibrosis	22110671	CNVD
Hirschsprung''s Disease	21712996	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:86 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:46649600-46649800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr4:46649600-46650200	Enhancers	ES-WA7 Cell Line	embryonic stem cell
3	chr4:46649800-46650200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
4	chr4:46649800-46650200	Enhancers	HUES6 Cell Line	embryonic stem cell
5	chr4:46649800-46650200	Enhancers	iPS-15b Cell Line	embryonic stem cell
6	chr4:46650000-46650200	Enhancers	ES-I3 Cell Line	embryonic stem cell
7	chr4:46650000-46650200	Enhancers	HUES48 Cell Line	embryonic stem cell
8	chr4:46655600-46656000	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
9	chr4:46657400-46659800	Enhancers	Fetal Intestine Large	intestine
10	chr4:46657800-46659600	Enhancers	Fetal Intestine Small	intestine
11	chr4:46658000-46658800	Enhancers	Fetal Kidney	kidney
12	chr4:46658200-46658800	Enhancers	Rectal Mucosa Donor 31	rectum
13	chr4:46659600-46660600	Weak transcription	Fetal Intestine Small	intestine
14	chr4:46660600-46661400	Enhancers	Fetal Intestine Small	intestine
15	chr4:46670600-46671200	Enhancers	Dnd41	blood
16	chr4:46676000-46677200	Enhancers	Fetal Brain Male	brain
17	chr4:46678200-46678800	Enhancers	iPS-20b Cell Line	embryonic stem cell
18	chr4:46678800-46679000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
19	chr4:46679000-46679400	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
20	chr4:46691200-46691600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
21	chr4:46691600-46692000	Enhancers	Cortex derived primary cultured neurospheres	brain
22	chr4:46700600-46701000	ZNF genes & repeats	iPS DF 6.9 Cell Line	embryonic stem cell
23	chr4:46700600-46701200	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
24	chr4:46700800-46701400	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
25	chr4:46701400-46701600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
26	chr4:46707400-46708600	Enhancers	Cortex derived primary cultured neurospheres	brain
27	chr4:46708600-46711200	Weak transcription	Cortex derived primary cultured neurospheres	brain
28	chr4:46711200-46712000	Enhancers	Cortex derived primary cultured neurospheres	brain
29	chr4:46720200-46720600	Enhancers	iPS-20b Cell Line	embryonic stem cell
30	chr4:46720200-46720800	Enhancers	ES-I3 Cell Line	embryonic stem cell
31	chr4:46720200-46720800	Enhancers	HUES48 Cell Line	embryonic stem cell
32	chr4:46720400-46720800	Enhancers	Fetal Brain Male	brain
33	chr4:46720400-46721200	Enhancers	iPS-15b Cell Line	embryonic stem cell
34	chr4:46720800-46722600	Weak transcription	Fetal Brain Male	brain
35	chr4:46722600-46723200	Enhancers	Fetal Brain Male	brain
36	chr4:46744600-46745400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
37	chr4:46748200-46749000	Enhancers	Brain Hippocampus Middle	brain
38	chr4:46766400-46770000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
39	chr4:46767400-46768200	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
40	chr4:46770000-46770200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
41	chr4:46783600-46784200	Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
42	chr4:46783600-46784200	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
43	chr4:46789600-46790000	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
44	chr4:46790000-46791400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
45	chr4:46793800-46794400	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
46	chr4:46794400-46794800	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
47	chr4:46794800-46795200	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
48	chr4:46795200-46795800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
49	chr4:46795800-46796400	Enhancers	iPS-18 Cell Line	embryonic stem cell
50	chr4:46795800-46797000	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links