Variant report

Variant	nsv1012672
Chromosome Location	chr2:184363204-184571778
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:496)
CpG islands
(count:305)
Chromatin interactive
region (count:13)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:496 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr2:184397205-184397664	H1-hESC	embryonic stem cell:	n/a	n/a
2	BATF	chr2:184395190-184395495	GM12878	blood:	n/a	n/a
3	BATF	chr2:184395172-184395470	GM12878	blood:	n/a	n/a
4	BCL11A	chr2:184543626-184543951	H1-hESC	embryonic stem cell:	n/a	n/a
5	BCL11A	chr2:184397325-184397593	H1-hESC	embryonic stem cell:	n/a	n/a
6	BCL11A	chr2:184543663-184543896	H1-hESC	embryonic stem cell:	n/a	n/a
7	BHLHE40	chr2:184406481-184406835	HepG2	liver:	n/a	n/a
8	BHLHE40	chr2:184395173-184395644	GM12878	blood:	n/a	n/a
9	CEBPB	chr2:184398647-184398825	HepG2	liver:	n/a	chr2:184398671-184398682
10	CEBPB	chr2:184507062-184507394	HepG2	liver:	n/a	chr2:184507200-184507211
11	CEBPB	chr2:184526429-184526718	HepG2	liver:	n/a	n/a
12	CEBPB	chr2:184431962-184432233	A549	lung:	n/a	chr2:184432078-184432089
13	CEBPB	chr2:184495870-184496106	IMR90	lung:	n/a	chr2:184495965-184495976 chr2:184495888-184495901
14	CEBPB	chr2:184431871-184432245	IMR90	lung:	n/a	chr2:184432078-184432089
15	CEBPB	chr2:184387339-184387348	HepG2	liver:	n/a	n/a
16	CEBPB	chr2:184495787-184496126	HepG2	liver:	n/a	chr2:184495965-184495976 chr2:184495888-184495901
17	CEBPB	chr2:184431962-184432138	K562	blood:	n/a	chr2:184432078-184432089
18	CEBPB	chr2:184406790-184407126	IMR90	lung:	n/a	n/a
19	CEBPB	chr2:184507144-184507344	IMR90	lung:	n/a	chr2:184507200-184507211
20	CEBPB	chr2:184406466-184407109	HepG2	liver:	n/a	n/a
21	CEBPB	chr2:184507110-184507516	A549	lung:	n/a	chr2:184507200-184507211
22	CEBPB	chr2:184431896-184432225	HepG2	liver:	n/a	chr2:184432078-184432089
23	CEBPB	chr2:184406844-184407126	A549	lung:	n/a	n/a
24	CEBPB	chr2:184533456-184533671	HepG2	liver:	n/a	n/a
25	CEBPB	chr2:184507035-184507391	H1-hESC	embryonic stem cell:	n/a	chr2:184507200-184507211
26	CEBPB	chr2:184495812-184496080	A549	lung:	n/a	chr2:184495965-184495976 chr2:184495888-184495901
27	CHD2	chr2:184543632-184543942	H1-hESC	embryonic stem cell:	n/a	n/a
28	CHD2	chr2:184375942-184375997	H1-hESC	embryonic stem cell:	n/a	n/a
29	CHD2	chr2:184470101-184470122	H1-hESC	embryonic stem cell:	n/a	n/a
30	CREB1	chr2:184397195-184397670	H1-hESC	embryonic stem cell:	n/a	n/a
31	CTCF	chr2:184473608-184473778	MCF-7	breast:	n/a	chr2:184473684-184473702 chr2:184473679-184473700
32	CTCF	chr2:184473647-184473762	HepG2	liver:	n/a	chr2:184473684-184473702 chr2:184473679-184473700
33	CTCF	chr2:184475614-184475691	H1-hESC	embryonic stem cell:	n/a	n/a
34	CTCF	chr2:184475600-184475750	HRPEpiC	eye:	n/a	n/a
35	CTCF	chr2:184473708-184473734	MCF-7	breast:	n/a	n/a
36	CTCF	chr2:184475580-184475730	HBMEC	blood vessel:	n/a	n/a
37	CTCF	chr2:184473670-184473703	GM19238	blood:	n/a	chr2:184473684-184473702 chr2:184473679-184473700
38	CTCF	chr2:184473542-184473882	GM12878	blood:	n/a	chr2:184473684-184473702 chr2:184473679-184473700
39	CTCF	chr2:184473660-184473810	GM06990	blood:	n/a	chr2:184473684-184473702 chr2:184473679-184473700
40	CTCF	chr2:184475600-184475750	HMEC	breast:	n/a	n/a
41	CTCF	chr2:184560954-184561033	MCF-7	breast:	n/a	n/a
42	CTCF	chr2:184560840-184560990	HMEC	breast:	n/a	n/a
43	CTCF	chr2:184475580-184475730	A549	lung:	n/a	n/a
44	CTCF	chr2:184423940-184424090	GM12875	blood:	n/a	n/a
45	CTCF	chr2:184475620-184475770	HRE	kidney:	n/a	n/a
46	CTCF	chr2:184475580-184475730	HepG2	liver:	n/a	n/a
47	CTCF	chr2:184475580-184475730	BE2_C	brain:	n/a	n/a
48	CTCF	chr2:184475520-184475670	HEK293	kidney:	n/a	n/a
49	CTCF	chr2:184376317-184376357	Kidney_OC	kidney:	n/a	n/a
50	CTCF	chr2:184372920-184373070	HepG2	liver:	n/a	n/a

(count:305 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:184531153-184531203	HEK293	kidney:	embryo
2	chr2:184472883-184472933	HEK293	kidney:	embryo
3	chr2:184475542-184475592	Hela-S3	cervix:	n/a
4	chr2:184472883-184472933	SKMC	muscle:	n/a
5	chr2:184531153-184531203	HRE	kidney:	n/a
6	chr2:184395412-184395462	MCF-7	breast:	n/a
7	chr2:184402122-184402172	A549	lung:	n/a
8	chr2:184475542-184475592	HMEC	breast:	n/a
9	chr2:184531153-184531203	PANC-1	pancreas:	n/a
10	chr2:184402122-184402172	BE2_C	brain:	n/a
11	chr2:184472883-184472933	HRCEpiC	kidney:	n/a
12	chr2:184472883-184472933	LNCaP	prostate:	n/a
13	chr2:184531153-184531203	AG09319	gingival:	n/a
14	chr2:184475542-184475592	SK-N-MC	brain:	n/a
15	chr2:184531153-184531203	H1-hESC	embryonic stem cell:	embryo
16	chr2:184395412-184395462	AG09319	gingival:	n/a
17	chr2:184475542-184475592	AG04449	skin:	fetal
18	chr2:184472883-184472933	HCT-116	colon:	n/a
19	chr2:184472883-184472933	GM12891	blood:	n/a
20	chr2:184472883-184472933	Jurkat	blood:	n/a
21	chr2:184472883-184472933	HAEpiC	amniotic membrane:	n/a
22	chr2:184402122-184402172	Hepatocyte	liver:	n/a
23	chr2:184531153-184531203	GM12878	blood:	n/a
24	chr2:184395412-184395462	HCF	heart:	n/a
25	chr2:184402122-184402172	K562	blood:	n/a
26	chr2:184402122-184402172	GM19239	blood:	n/a
27	chr2:184475542-184475592	GM12878	blood:	n/a
28	chr2:184472883-184472933	GM06990	blood:	n/a
29	chr2:184475542-184475592	GM06990	blood:	n/a
30	chr2:184531153-184531203	GM06990	blood:	n/a
31	chr2:184402122-184402172	PANC-1	pancreas:	n/a
32	chr2:184395412-184395462	Jurkat	blood:	n/a
33	chr2:184475542-184475592	PFSK-1	brain:	n/a
34	chr2:184395412-184395462	RPTEC	kidney:	n/a
35	chr2:184395412-184395462	HL-60	blood:	n/a
36	chr2:184531153-184531203	BJ	skin:	n/a
37	chr2:184395412-184395462	H1-hESC	embryonic stem cell:	embryo
38	chr2:184402122-184402172	T-47D	breast:	n/a
39	chr2:184395412-184395462	ProgFib	skin:	n/a
40	chr2:184402122-184402172	HCPEpiC	choroid plexus:	n/a
41	chr2:184395412-184395462	HepG2	liver:	n/a
42	chr2:184475542-184475592	SK-N-SH_RA	brain:	n/a
43	chr2:184395412-184395462	HRPEpiC	eye:	n/a
44	chr2:184472883-184472933	K562	blood:	n/a
45	chr2:184402122-184402172	HepG2	liver:	n/a
46	chr2:184472883-184472933	SAEC	small airway:	n/a
47	chr2:184395412-184395462	GM12891	blood:	n/a
48	chr2:184531153-184531203	BE2_C	brain:	n/a
49	chr2:184402122-184402172	Caco-2	colon:	n/a
50	chr2:184531153-184531203	SK-N-MC	brain:	n/a

(count:13 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:184441021..184443496-chr2:184443583..184445745,2	MCF-7	breast:
2	chr2:184416367..184418824-chr2:184421256..184423003,2	K562	blood:
3	chr2:184420912..184422678-chr2:184425750..184427792,2	K562	blood:
4	chr2:184441021..184443496-chr2:184443583..184445745,2	MCF-7	breast:
5	chr2:184357852..184360567-chr2:184368359..184370734,2	K562	blood:
6	chr2:184533926..184535731-chr2:184543881..184546242,2	MCF-7	breast:
7	chr2:184387652..184388652-chr5:19684075..19684575,2	MCF-7	breast:
8	chr2:184476716..184479514-chr2:184486721..184488223,2	K562	blood:
9	chr2:184416367..184418824-chr2:184421256..184423003,2	K562	blood:
10	chr2:184420912..184422678-chr2:184425750..184427792,2	K562	blood:
11	chr18:21061627..21062127-chr2:184416573..184417102,2	MCF-7	breast:
12	chr2:184533926..184535731-chr2:184543881..184546242,2	MCF-7	breast:
13	chr2:184476716..184479514-chr2:184486721..184488223,2	K562	blood:

No data

Variant related genes	Relation type
CACYBPP2	TF binding region
CACYBPP2	CpG island

Extended variants
information (count: 3862 )
Associated
traits (count: 54 )

Variant overlapped rSNPs/rCNVs (count:3862 , 50 per page) page: 1 2 3 4 5 6 7 ... 78

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs550892579	chr2:184367036-184367037	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs533952388	chr2:184367046-184367047	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs13400364	chr2:184367088-184367089	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs180853613	chr2:184367151-184367152	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs2118477	chr2:184367212-184367213	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs113117295	chr2:184367243-184367244	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs540006297	chr2:184367254-184367255	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs536293261	chr2:184367273-184367274	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs533146181	chr2:184367298-184367299	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs560409255	chr2:184367308-184367309	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs11676026	chr2:184367502-184367503	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs552284514	chr2:184367524-184367525	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs566586474	chr2:184367599-184367600	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs562597959	chr2:184367602-184367603	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs535171063	chr2:184367620-184367621	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs531202853	chr2:184367649-184367650	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs548206307	chr2:184367660-184367661	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs114875936	chr2:184367696-184367697	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs67951091	chr2:184367707-184367708	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs66879817	chr2:184367722-184367723	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs566741131	chr2:184367746-184367747	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs146210379	chr2:184367750-184367751	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs142047188	chr2:184367820-184367821	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs185253046	chr2:184367839-184367840	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs139339966	chr2:184367859-184367860	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs12613514	chr2:184367912-184367913	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs554951858	chr2:184367946-184367947	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs564926106	chr2:184367957-184367958	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs189720408	chr2:184367975-184367976	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs554140296	chr2:184367995-184367996	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs34017793	chr2:184372037-184372038	ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs10931084	chr2:184372041-184372042	ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs578024994	chr2:184372053-184372054	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
34	rs368649044	chr2:184372061-184372062	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
35	rs529862192	chr2:184372069-184372070	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
36	rs563833248	chr2:184372076-184372077	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
37	rs137946707	chr2:184372096-184372097	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
38	rs188005396	chr2:184372098-184372099	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
39	rs559179179	chr2:184372142-184372143	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
40	rs180917250	chr2:184372157-184372158	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
41	rs185368580	chr2:184372158-184372159	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
42	rs142417609	chr2:184372159-184372160	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
43	rs530770908	chr2:184372164-184372165	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
44	rs550385728	chr2:184372183-184372184	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
45	rs546969657	chr2:184372251-184372252	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
46	rs567403580	chr2:184372271-184372272	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
47	rs536246628	chr2:184372293-184372294	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
48	rs546629739	chr2:184372310-184372311	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
49	rs189768479	chr2:184372326-184372327	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
50	rs374770322	chr2:184372351-184372352	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:54)

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
Autism	18522746	CNVD
Melanoma	18172304	CNVD
Cancer	16751803	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21980252	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
Hodgkin''s lymphoma	17606441	CNVD
Lung cancer	18438408	CNVD
Glioblastoma	21080181	CNVD
Prostate cancer	18632612	CNVD
Acute myeloid leukemia	20729466	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
small cell lung cancer	20016488	CNVD
Facial dysmorphism	20548289	CNVD
Mental retardation	20548289	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Breast cancer	21364760	CNVD
Myelofibrosis	22110671	CNVD
Hirschsprung''s Disease	21712996	CNVD
Cancer	21183584	CNVD
Sudden cardiac death	19188705	CNVD
Autism	19329560	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Obesity	21131291	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:334 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:184367000-184367800	Enhancers	HMEC	breast
2	chr2:184367200-184368000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr2:184372000-184372400	ZNF genes & repeats	ES-I3 Cell Line	embryonic stem cell
4	chr2:184372400-184374800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
5	chr2:184373400-184374400	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
6	chr2:184374200-184375400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
7	chr2:184374400-184376800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
8	chr2:184375000-184375400	Enhancers	HUES48 Cell Line	embryonic stem cell
9	chr2:184376400-184377000	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
10	chr2:184376800-184378200	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
11	chr2:184378200-184385000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
12	chr2:184381200-184381400	Enhancers	Rectal Mucosa Donor 31	rectum
13	chr2:184382800-184383200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
14	chr2:184383200-184383600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
15	chr2:184383400-184383800	Enhancers	Pancreas	Pancrea
16	chr2:184383400-184385200	Enhancers	Fetal Intestine Small	intestine
17	chr2:184383600-184383800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
18	chr2:184383800-184385000	Weak transcription	Pancreas	Pancrea
19	chr2:184383800-184393800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
20	chr2:184384000-184384600	Enhancers	Psoas Muscle	Psoas
21	chr2:184384000-184385200	Enhancers	Fetal Intestine Large	intestine
22	chr2:184385000-184385200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
23	chr2:184385000-184385800	Enhancers	Pancreas	Pancrea
24	chr2:184385200-184385600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
25	chr2:184385600-184386000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
26	chr2:184386400-184387800	Enhancers	Pancreatic Islets	Pancreatic Islet
27	chr2:184387400-184387800	Enhancers	Fetal Heart	heart
28	chr2:184392600-184392800	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
29	chr2:184392800-184393600	Weak transcription	HUES6 Cell Line	embryonic stem cell
30	chr2:184393200-184394200	Enhancers	ES-I3 Cell Line	embryonic stem cell
31	chr2:184393600-184394400	Enhancers	H9 Cell Line	embryonic stem cell
32	chr2:184393600-184395000	Enhancers	HUES48 Cell Line	embryonic stem cell
33	chr2:184393600-184397600	Enhancers	HUES6 Cell Line	embryonic stem cell
34	chr2:184393600-184398200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
35	chr2:184393800-184394400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
36	chr2:184393800-184394800	Enhancers	H1 Cell Line	embryonic stem cell
37	chr2:184393800-184395600	Enhancers	HUES64 Cell Line	embryonic stem cell
38	chr2:184393800-184395600	Enhancers	iPS-18 Cell Line	embryonic stem cell
39	chr2:184393800-184397200	Enhancers	iPS-20b Cell Line	embryonic stem cell
40	chr2:184393800-184397600	Enhancers	iPS-15b Cell Line	embryonic stem cell
41	chr2:184394200-184394600	Flanking Active TSS	ES-I3 Cell Line	embryonic stem cell
42	chr2:184394400-184395000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
43	chr2:184394400-184397800	Weak transcription	H9 Cell Line	embryonic stem cell
44	chr2:184394600-184397200	Enhancers	ES-I3 Cell Line	embryonic stem cell
45	chr2:184394800-184397600	Weak transcription	H1 Cell Line	embryonic stem cell
46	chr2:184395000-184395200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
47	chr2:184395000-184395200	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
48	chr2:184395200-184395400	Enhancers	HUES48 Cell Line	embryonic stem cell
49	chr2:184395200-184397400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
50	chr2:184395400-184397000	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links