Variant report

Variant	nsv1004762
Chromosome Location	chr3:97935701-98000227
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:295)
CpG islands
(count:244)
Chromatin interactive
region (count:3)
LncRNA
region (count:11)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:295 , 50 per page) page: 1 2 3 4 5 6

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr3:97962650-97963075	HepG2	liver:	n/a	n/a
2	BATF	chr3:97959089-97959288	GM12878	blood:	n/a	chr3:97959202-97959213
3	BATF	chr3:97952380-97952574	GM12878	blood:	n/a	n/a
4	BCL11A	chr3:97952351-97952515	GM12878	blood:	n/a	n/a
5	BCL11A	chr3:97951400-97951563	GM12878	blood:	n/a	n/a
6	BHLHE40	chr3:97943474-97943485	GM12878	blood:	n/a	n/a
7	BHLHE40	chr3:97951405-97952685	GM12878	blood:	n/a	n/a
8	BHLHE40	chr3:97962720-97963131	HepG2	liver:	n/a	n/a
9	BRCA1	chr3:97939937-97940001	GM12878	blood:	n/a	n/a
10	CEBPB	chr3:97962794-97963080	HepG2	liver:	n/a	n/a
11	CEBPB	chr3:97984146-97984209	HepG2	liver:	n/a	chr3:97984150-97984161
12	CHD1	chr3:97959991-97960022	H1-hESC	embryonic stem cell:	n/a	n/a
13	CHD1	chr3:97952484-97952829	GM12878	blood:	n/a	n/a
14	CHD1	chr3:97942962-97942975	GM12878	blood:	n/a	n/a
15	CHD2	chr3:97952077-97952654	GM12878	blood:	n/a	n/a
16	CTCF	chr3:97978720-97978870	HUVEC	blood vessel:	n/a	n/a
17	CTCF	chr3:97978700-97978850	GM12868	blood:	n/a	n/a
18	CTCF	chr3:97978900-97979050	Caco-2	colon:	n/a	n/a
19	CTCF	chr3:97978720-97978870	HMF	breast:	n/a	n/a
20	CTCF	chr3:97978740-97978890	HEEpiC	esophagus:	n/a	n/a
21	CTCF	chr3:97978708-97978833	MCF-7	breast:	n/a	n/a
22	CTCF	chr3:97978572-97978895	H1-hESC	embryonic stem cell:	n/a	n/a
23	CTCF	chr3:97978660-97978810	GM12865	blood:	n/a	n/a
24	CTCF	chr3:97978747-97978818	K562	blood:	n/a	n/a
25	CTCF	chr3:97978720-97978870	GM12864	blood:	n/a	n/a
26	CTCF	chr3:97978760-97978910	GM06990	blood:	n/a	n/a
27	CTCF	chr3:97978700-97978850	RPTEC	kidney:	n/a	n/a
28	CTCF	chr3:97978710-97978873	HUVEC	blood vessel:	n/a	n/a
29	CTCF	chr3:97978719-97978887	Medullo	brain:	n/a	n/a
30	CTCF	chr3:97978753-97978801	GM10248	blood:	n/a	n/a
31	CTCF	chr3:97978720-97978870	HepG2	liver:	n/a	n/a
32	CTCF	chr3:97978720-97978870	GM12870	blood:	n/a	n/a
33	CTCF	chr3:97978740-97978890	GM12865	blood:	n/a	n/a
34	CTCF	chr3:97978720-97978870	GM12867	blood:	n/a	n/a
35	CTCF	chr3:97978740-97978890	BE2_C	brain:	n/a	n/a
36	CTCF	chr3:97978594-97978885	H1-hESC	embryonic stem cell:	n/a	n/a
37	CTCF	chr3:97978680-97978830	K562	blood:	n/a	n/a
38	CTCF	chr3:97978700-97978850	AG04450	lung:	n/a	n/a
39	CTCF	chr3:97978640-97978790	HRE	kidney:	n/a	n/a
40	CTCF	chr3:97978751-97978794	ProgFib	skin:	n/a	n/a
41	CTCF	chr3:97978740-97978890	GM12866	blood:	n/a	n/a
42	CTCF	chr3:97978686-97978852	MCF-7	breast:	n/a	n/a
43	CTCF	chr3:97978720-97978870	GM12868	blood:	n/a	n/a
44	CTCF	chr3:97978713-97978847	GM20000	blood:	n/a	n/a
45	CTCF	chr3:97952360-97952510	GM12873	blood:	n/a	n/a
46	CTCF	chr3:97978720-97978870	SAEC	small airway:	n/a	n/a
47	CTCF	chr3:97978640-97978790	GM12878	blood:	n/a	n/a
48	CTCF	chr3:97978680-97978830	GM12869	blood:	n/a	n/a
49	CTCF	chr3:97978680-97978830	GM12871	blood:	n/a	n/a
50	CTCF	chr3:97978660-97978810	GM12874	blood:	n/a	n/a

(count:244 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:97983253-97983303	GM19239	blood:	n/a
2	chr3:97982830-97982880	SAEC	small airway:	n/a
3	chr3:97982830-97982880	Hela-S3	cervix:	n/a
4	chr3:97982397-97982447	GM12891	blood:	n/a
5	chr3:97983253-97983303	IMR90	lung:	fetal
6	chr3:97983253-97983303	HRCEpiC	kidney:	n/a
7	chr3:97983253-97983303	HIPEpiC	eye:	n/a
8	chr3:97982397-97982447	HRCEpiC	kidney:	n/a
9	chr3:97982397-97982447	SK-N-MC	brain:	n/a
10	chr3:97982397-97982447	AG09319	gingival:	n/a
11	chr3:97982830-97982880	HRE	kidney:	n/a
12	chr3:97982397-97982447	IMR90	lung:	fetal
13	chr3:97983253-97983303	NT2-D1	testis:	n/a
14	chr3:97983253-97983303	NHBE	bronchial:	n/a
15	chr3:97982397-97982447	HNPCEpiC	eye:	n/a
16	chr3:97982830-97982880	NT2-D1	testis:	n/a
17	chr3:97983253-97983303	NB4	blood:	n/a
18	chr3:97982830-97982880	AG10803	skin:	n/a
19	chr3:97982397-97982447	BE2_C	brain:	n/a
20	chr3:97983253-97983303	MCF-7	breast:	n/a
21	chr3:97982830-97982880	PFSK-1	brain:	n/a
22	chr3:97983253-97983303	GM12878	blood:	n/a
23	chr3:97983253-97983303	HNPCEpiC	eye:	n/a
24	chr3:97982397-97982447	BJ	skin:	n/a
25	chr3:97983253-97983303	HCT-116	colon:	n/a
26	chr3:97983253-97983303	ECC-1	luminal epithelium:	n/a
27	chr3:97983253-97983303	HAEpiC	amniotic membrane:	n/a
28	chr3:97982397-97982447	HPAEpiC	pulmonary alveolar:	n/a
29	chr3:97983253-97983303	BE2_C	brain:	n/a
30	chr3:97983253-97983303	NH-A	brain:	n/a
31	chr3:97983253-97983303	H1-hESC	embryonic stem cell:	embryo
32	chr3:97982830-97982880	MCF-7	breast:	n/a
33	chr3:97983253-97983303	HL-60	blood:	n/a
34	chr3:97982397-97982447	SAEC	small airway:	n/a
35	chr3:97983253-97983303	SK-N-MC	brain:	n/a
36	chr3:97983253-97983303	AG04450	lung:	fetal
37	chr3:97983253-97983303	GM06990	blood:	n/a
38	chr3:97983540-97983590	H1-hESC	embryonic stem cell:	embryo
39	chr3:97982397-97982447	HMEC	breast:	n/a
40	chr3:97983540-97983590	GM06990	blood:	n/a
41	chr3:97982830-97982880	HAEpiC	amniotic membrane:	n/a
42	chr3:97982397-97982447	Jurkat	blood:	n/a
43	chr3:97982397-97982447	LNCaP	prostate:	n/a
44	chr3:97983540-97983590	Hela-S3	cervix:	n/a
45	chr3:97983540-97983590	CMK	blood:	n/a
46	chr3:97983540-97983590	AG09309	skin:	n/a
47	chr3:97982397-97982447	CMK	blood:	n/a
48	chr3:97983540-97983590	AG04449	skin:	fetal
49	chr3:97983540-97983590	U87	brain:	n/a
50	chr3:97983253-97983303	PANC-1	pancreas:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr3:97977847..97980147-chr3:97980537..97982058,2	MCF-7	breast:
2	chr3:97978738..97980851-chr3:98012803..98015207,2	MCF-7	breast:
3	chr3:97977847..97980147-chr3:97980537..97982058,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-MINA-2	chr3:97955718-97955882	XLOC_003187
2	lnc-MINA-2	chr3:97956121-97956211	XLOC_003187
3	lnc-MINA-2	chr3:97956121-97956219	XLOC_003187
4	lnc-MINA-2	chr3:97949910-97950089	XLOC_003187
5	lnc-OR5H6-1	chr3:97952495-97952520	ENSG00000251088.1
6	lnc-MINA-2	chr3:97956121-97956217	XLOC_003187
7	lnc-MINA-2	chr3:97954530-97954692	XLOC_003187
8	lnc-MINA-2	chr3:97949910-97950089	XLOC_003187
9	lnc-MINA-2	chr3:97955718-97955882	XLOC_003187
10	lnc-MINA-2	chr3:97954345-97954692	XLOC_003187
11	lnc-MINA-2	chr3:97955718-97955882	XLOC_003187

No data

Variant related genes	Relation type
OR5H6	TF binding region
ENSG00000251088	TF binding region
OR5H7P	TF binding region
OR5H4P	TF binding region
OR5H2	TF binding region
OR5H6	CpG island
ENSG00000251088	CpG island
OR5H7P	CpG island
OR5H4P	CpG island
OR5H2	CpG island
POU2F1	miRNA target sites

Extended variants
information (count: 1654 )
Associated
traits (count: 53 )

Variant overlapped rSNPs/rCNVs (count:1654 , 50 per page) page: 1 2 3 4 5 6 7 ... 34

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs551387119	chr3:97935720-97935721	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs543587391	chr3:97935748-97935749	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs571402020	chr3:97935753-97935754	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs79483703	chr3:97935769-97935770	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs189892900	chr3:97935782-97935783	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs191549154	chr3:97935822-97935823	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs115035909	chr3:97935833-97935834	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs553289733	chr3:97935848-97935849	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs139304472	chr3:97935852-97935853	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs4463010	chr3:97935901-97935902	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs386663711	chr3:97935921-97935922	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs4463011	chr3:97935927-97935928	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs72929022	chr3:97935939-97935940	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs561063393	chr3:97935962-97935963	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs530122791	chr3:97935975-97935976	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs4624601	chr3:97936004-97936005	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs149434703	chr3:97936015-97936016	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs183891398	chr3:97936038-97936039	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs62267183	chr3:97936045-97936046	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs4452364	chr3:97936050-97936051	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs189060194	chr3:97936110-97936111	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs529211022	chr3:97936124-97936125	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs138350867	chr3:97936127-97936128	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs538839160	chr3:97936141-97936142	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs4452365	chr3:97936149-97936150	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs530936393	chr3:97936167-97936168	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs56957104	chr3:97936176-97936177	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs550768869	chr3:97936191-97936192	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs4464499	chr3:97936249-97936250	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs4286458	chr3:97936264-97936265	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs553251018	chr3:97936266-97936267	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs566764628	chr3:97936291-97936292	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs375608025	chr3:97936296-97936297	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs79798500	chr3:97936297-97936298	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs181503717	chr3:97936311-97936312	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs66498739	chr3:97936333-97936334	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs566875756	chr3:97936336-97936337	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs544213755	chr3:97936339-97936340	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs554351001	chr3:97936350-97936351	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs4482695	chr3:97936358-97936359	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs144775211	chr3:97936385-97936386	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs13081420	chr3:97936386-97936387	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs148149596	chr3:97936419-97936420	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs367557498	chr3:97936432-97936433	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs115534646	chr3:97936474-97936475	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs35327048	chr3:97936490-97936491	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs550981343	chr3:97936491-97936492	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs34573833	chr3:97936500-97936501	Enhancers Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs530258168	chr3:97936517-97936518	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs76626237	chr3:97936531-97936532	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:53)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Glioblastoma multiforme	21080181	CNVD
Retinoblastoma	21504564	CNVD
Renal cell carcinoma	21668985	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	17603634	CNVD
Uveal melanoma	20484589	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
Hirschsprung''s Disease	21712996	CNVD
Hepatocellular carcinoma	16750200	CNVD
Cancer	21183584	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Bipolar disorder	20877625	CNVD
Bipolar disorder	21956041	CNVD
Bipolar disorder	22241247	CNVD
Biliary cancer	18923514	CNVD
Prostate cancer	21965145	CNVD
Cancer	21129771	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Cervical cancer	21062161	CNVD
Squamous cell cancer	20885788	CNVD
Melanoma	18172304	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Bipolar disorder	18458673	CNVD
Breast cancer	22032731	CNVD
Neurodevelopmental disorder	22521361	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Breast cancer	16461572	CNVD
Neuroblastoma	17533364	CNVD
microdeletion syndrome	22180640	CNVD
Cervical Cancer	21857958	CNVD
Melanoma	21693616	CNVD
Lung cancer	21426551	CNVD
Cancer	21637783	CNVD
Cervical cancer	21063398	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Oral cancer	21386901	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	22065749	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Myelofibrosis	22110671	CNVD
Epilepsy	21858020	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	22522925	CNVD

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:97928200-97936800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
2	chr3:97932800-97936200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
3	chr3:97933800-97938000	Weak transcription	HUES64 Cell Line	embryonic stem cell
4	chr3:97936200-97936800	Enhancers	ES-I3 Cell Line	embryonic stem cell
5	chr3:97936800-97937600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
6	chr3:97936800-97937800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
7	chr3:97937600-97938000	Enhancers	ES-I3 Cell Line	embryonic stem cell
8	chr3:97937800-97942400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
9	chr3:97938000-97938200	Enhancers	HUES64 Cell Line	embryonic stem cell
10	chr3:97942400-97943400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
11	chr3:97943400-97944000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
12	chr3:97944000-97944200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
13	chr3:97945200-97945600	Active TSS	Esophagus	oesophagus
14	chr3:97951200-97952800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
15	chr3:97951400-97952200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
16	chr3:97951600-97952800	Enhancers	Primary hematopoietic stem cells short term culture	blood
17	chr3:97951800-97952200	Enhancers	Primary hematopoietic stem cells	blood
18	chr3:97952200-97952600	Flanking Active TSS	Primary hematopoietic stem cells	blood
19	chr3:97952200-97952600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
20	chr3:97952600-97953400	Enhancers	Primary hematopoietic stem cells	blood
21	chr3:97952600-97953600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
22	chr3:97958600-97959400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
23	chr3:97959000-97959600	Enhancers	iPS-18 Cell Line	embryonic stem cell
24	chr3:97959000-97961600	Enhancers	HUES48 Cell Line	embryonic stem cell
25	chr3:97959200-97960600	Enhancers	H9 Cell Line	embryonic stem cell
26	chr3:97959200-97961400	Enhancers	HUES6 Cell Line	embryonic stem cell
27	chr3:97959200-97961400	Enhancers	iPS-20b Cell Line	embryonic stem cell
28	chr3:97959200-97961800	Enhancers	HUES64 Cell Line	embryonic stem cell
29	chr3:97959400-97961400	Enhancers	iPS-15b Cell Line	embryonic stem cell
30	chr3:97959600-97960000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
31	chr3:97959800-97960400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
32	chr3:97959800-97960600	Enhancers	H1 Cell Line	embryonic stem cell
33	chr3:97959800-97962000	Enhancers	ES-I3 Cell Line	embryonic stem cell
34	chr3:97960000-97961800	Enhancers	iPS-18 Cell Line	embryonic stem cell
35	chr3:97962600-97964000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
36	chr3:97970200-97973400	Weak transcription	Fetal Heart	heart
37	chr3:97974200-97974400	Enhancers	iPS-20b Cell Line	embryonic stem cell
38	chr3:97974400-97975000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
39	chr3:97974600-97975400	Enhancers	ES-I3 Cell Line	embryonic stem cell
40	chr3:97974600-97975800	Enhancers	HUES48 Cell Line	embryonic stem cell
41	chr3:97974600-97975800	Enhancers	iPS-18 Cell Line	embryonic stem cell
42	chr3:97974800-97975400	Enhancers	H1 Cell Line	embryonic stem cell
43	chr3:97974800-97975400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
44	chr3:97975000-97975600	Enhancers	iPS-20b Cell Line	embryonic stem cell
45	chr3:97975200-97975600	Enhancers	HUES64 Cell Line	embryonic stem cell
46	chr3:97989600-97990000	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
47	chr3:97990000-97991000	Weak transcription	HUES6 Cell Line	embryonic stem cell
48	chr3:97990400-97991600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
49	chr3:97991000-97991200	Enhancers	HUES6 Cell Line	embryonic stem cell
50	chr3:97993000-97993400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell

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