Variant report

Variant	nsv432462
Chromosome Location	chr3:97918267-98001710
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:310)
CpG islands
(count:366)
Chromatin interactive
region (count:3)
LncRNA
region (count:13)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:310 , 50 per page) page: 1 2 3 4 5 6 7

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	chr3:97962720-97963131	HepG2	liver:	n/a	n/a
7	BHLHE40	chr3:97943474-97943485	GM12878	blood:	n/a	n/a
8	BHLHE40	chr3:97951405-97952685	GM12878	blood:	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	CEBPB	chr3:97922385-97922736	HepG2	liver:	n/a	chr3:97922556-97922567
13	CEBPB	chr3:97922385-97922691	A549	lung:	n/a	chr3:97922556-97922567
14	CHD1	chr3:97959991-97960022	H1-hESC	embryonic stem cell:	n/a	n/a
15	CHD1	chr3:97952484-97952829	GM12878	blood:	n/a	n/a
16	CHD1	chr3:97942962-97942975	GM12878	blood:	n/a	n/a
17	CHD2	chr3:97952077-97952654	GM12878	blood:	n/a	n/a
18	CTCF	chr3:97978668-97978886	H1-hESC	embryonic stem cell:	n/a	n/a
19	CTCF	chr3:97978720-97978870	GM12869	blood:	n/a	n/a
20	CTCF	chr3:97978683-97978863	GM12891	blood:	n/a	n/a
21	CTCF	chr3:97978640-97978899	GM19238	blood:	n/a	n/a
22	CTCF	chr3:97978700-97978850	GM12868	blood:	n/a	n/a
23	CTCF	chr3:97978740-97978890	GM12875	blood:	n/a	n/a
24	CTCF	chr3:97978670-97978895	Gliobla	brain:	n/a	n/a
25	CTCF	chr3:97978572-97978895	H1-hESC	embryonic stem cell:	n/a	n/a
26	CTCF	chr3:97978760-97978910	GM06990	blood:	n/a	n/a
27	CTCF	chr3:97978594-97978885	H1-hESC	embryonic stem cell:	n/a	n/a
28	CTCF	chr3:97978680-97978830	GM12872	blood:	n/a	n/a
29	CTCF	chr3:97978660-97978810	NHEK	skin:	n/a	n/a
30	CTCF	chr3:97978726-97978848	GM10266	blood:	n/a	n/a
31	CTCF	chr3:97978620-97978770	RPTEC	kidney:	n/a	n/a
32	CTCF	chr3:97978700-97978850	HVMF	connective:	n/a	n/a
33	CTCF	chr3:97978700-97978850	HEK293	kidney:	n/a	n/a
34	CTCF	chr3:97978653-97978881	GM12892	blood:	n/a	n/a
35	CTCF	chr3:97978710-97978873	HUVEC	blood vessel:	n/a	n/a
36	CTCF	chr3:97978699-97978840	MCF-7	breast:	n/a	n/a
37	CTCF	chr3:97978680-97978830	K562	blood:	n/a	n/a
38	CTCF	chr3:97978690-97978822	LNCaP	prostate:	n/a	n/a
39	CTCF	chr3:97978440-97978509	GM19240	blood:	n/a	n/a
40	CTCF	chr3:97978686-97978852	MCF-7	breast:	n/a	n/a
41	CTCF	chr3:97978640-97978790	HPAF	blood vessel:	n/a	n/a
42	CTCF	chr3:97978690-97978878	GM13977	blood:	n/a	n/a
43	CTCF	chr3:97978747-97978818	K562	blood:	n/a	n/a
44	CTCF	chr3:97978660-97978810	BE2_C	brain:	n/a	n/a
45	CTCF	chr3:97978684-97978865	HepG2	liver:	n/a	n/a
46	CTCF	chr3:97978740-97978890	HL-60	blood:	n/a	n/a
47	CTCF	chr3:97978700-97978850	HEEpiC	esophagus:	n/a	n/a
48	CTCF	chr3:97978740-97978890	SAEC	small airway:	n/a	n/a
49	CTCF	chr3:97978440-97978590	GM12872	blood:	n/a	n/a
50	CTCF	chr3:97924040-97924190	GM12869	blood:	n/a	n/a

(count:366 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:98001269-98001319	CMK	blood:	n/a
2	chr3:98000733-98000783	A549	lung:	n/a
3	chr3:97982397-97982447	A549	lung:	n/a
4	chr3:98001269-98001319	MCF10A-Er-Src	breast:	n/a
5	chr3:97983253-97983303	PFSK-1	brain:	n/a
6	chr3:98000733-98000783	T-47D	breast:	n/a
7	chr3:98000733-98000783	NT2-D1	testis:	n/a
8	chr3:97983540-97983590	GM06990	blood:	n/a
9	chr3:97983540-97983590	LNCaP	prostate:	n/a
10	chr3:97983253-97983303	HAEpiC	amniotic membrane:	n/a
11	chr3:97982830-97982880	AG09319	gingival:	n/a
12	chr3:97982830-97982880	NB4	blood:	n/a
13	chr3:98000733-98000783	ECC-1	luminal epithelium:	n/a
14	chr3:97982830-97982880	PFSK-1	brain:	n/a
15	chr3:97982830-97982880	RPTEC	kidney:	n/a
16	chr3:97983253-97983303	SK-N-SH	brain:	n/a
17	chr3:98000733-98000783	HEEpiC	esophagus:	n/a
18	chr3:97982397-97982447	HRE	kidney:	n/a
19	chr3:97983253-97983303	HPAEpiC	pulmonary alveolar:	n/a
20	chr3:98001269-98001319	NHDF-neo	bronchial:	n/a
21	chr3:97982830-97982880	LNCaP	prostate:	n/a
22	chr3:97982830-97982880	AG04450	lung:	fetal
23	chr3:97982397-97982447	HEK293	kidney:	embryo
24	chr3:97982830-97982880	U87	brain:	n/a
25	chr3:97983540-97983590	A549	lung:	n/a
26	chr3:97983540-97983590	AG09309	skin:	n/a
27	chr3:98000733-98000783	HIPEpiC	eye:	n/a
28	chr3:97982397-97982447	ECC-1	luminal epithelium:	n/a
29	chr3:97983253-97983303	LNCaP	prostate:	n/a
30	chr3:97982397-97982447	HNPCEpiC	eye:	n/a
31	chr3:97983253-97983303	U87	brain:	n/a
32	chr3:97982830-97982880	HMEC	breast:	n/a
33	chr3:98001269-98001319	ovcar-3	ovarian:	n/a
34	chr3:97983253-97983303	HUVEC	blood vessel:	n/a
35	chr3:97983253-97983303	HepG2	liver:	n/a
36	chr3:98001269-98001319	PFSK-1	brain:	n/a
37	chr3:97982830-97982880	AG09309	skin:	n/a
38	chr3:97982397-97982447	MCF10A-Er-Src	breast:	n/a
39	chr3:97983540-97983590	HL-60	blood:	n/a
40	chr3:98000733-98000783	SAEC	small airway:	n/a
41	chr3:97982830-97982880	GM12892	blood:	n/a
42	chr3:97982397-97982447	NHDF-neo	bronchial:	n/a
43	chr3:97983540-97983590	H1-hESC	embryonic stem cell:	embryo
44	chr3:97982830-97982880	GM12878	blood:	n/a
45	chr3:98000733-98000783	MCF10A-Er-Src	breast:	n/a
46	chr3:97982830-97982880	AG10803	skin:	n/a
47	chr3:98001269-98001319	HEEpiC	esophagus:	n/a
48	chr3:97982397-97982447	AG09309	skin:	n/a
49	chr3:98001269-98001319	Hepatocyte	liver:	n/a
50	chr3:98001269-98001319	IMR90	lung:	fetal

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

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

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-MINA-6	chr3:97923366-97923509	NONHSAT090787
2	lnc-MINA-2	chr3:97954530-97954692	XLOC_003187
3	lnc-MINA-2	chr3:97956121-97956211	XLOC_003187
4	lnc-MINA-2	chr3:97956121-97956219	XLOC_003187
5	lnc-MINA-2	chr3:97949910-97950089	XLOC_003187
6	lnc-OR5H6-1	chr3:97952495-97952520	ENSG00000251088.1
7	lnc-MINA-6	chr3:97925331-97925450	NONHSAT090787
8	lnc-MINA-2	chr3:97949910-97950089	XLOC_003187
9	lnc-MINA-2	chr3:97955718-97955882	XLOC_003187
10	lnc-MINA-2	chr3:97955718-97955882	XLOC_003187
11	lnc-MINA-2	chr3:97954345-97954692	XLOC_003187
12	lnc-MINA-2	chr3:97956121-97956217	XLOC_003187
13	lnc-MINA-2	chr3:97955718-97955882	XLOC_003187

No data

Variant related genes	Relation type
OR5H6	TF binding region
OR5H7P	TF binding region
OR5H4P	TF binding region
OR5H3P	TF binding region
ENSG00000251088	TF binding region
OR5H2	TF binding region
OR5H6	CpG island
OR5H7P	CpG island
OR5H4P	CpG island
OR5H3P	CpG island
ENSG00000251088	CpG island
OR5H2	CpG island
POU2F1	miRNA target sites

Extended variants
information (count: 2714 )
Associated
traits (count: 54 )

Variant overlapped rSNPs/rCNVs (count:2714 , 50 per page) page: 1 2 3 4 5 6 7 ... 55

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2291810	chr3:97918267-97918268	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs549347373	chr3:97918287-97918288	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs547802395	chr3:97918298-97918299	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs569510959	chr3:97918300-97918301	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs377002246	chr3:97918313-97918314	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs539917620	chr3:97918314-97918315	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs556728146	chr3:97918337-97918338	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs78537156	chr3:97918355-97918356	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs370165632	chr3:97918370-97918371	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs539663298	chr3:97918392-97918393	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs191725448	chr3:97918404-97918405	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs572265054	chr3:97918448-97918449	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs141879449	chr3:97918467-97918468	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs557330467	chr3:97918486-97918487	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs181506681	chr3:97918489-97918490	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs72927072	chr3:97918535-97918536	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs566565237	chr3:97918547-97918548	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs563015155	chr3:97918559-97918560	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs9840421	chr3:97918560-97918561	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs542365844	chr3:97918572-97918573	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs377520899	chr3:97918603-97918604	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs562181852	chr3:97918606-97918607	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs9879316	chr3:97918614-97918615	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs186441131	chr3:97918638-97918639	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs564457175	chr3:97918701-97918702	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs533330052	chr3:97918706-97918707	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs190713301	chr3:97918734-97918735	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs554233661	chr3:97918742-97918743	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs570086826	chr3:97918752-97918753	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs535586900	chr3:97918781-97918782	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs549153983	chr3:97918782-97918783	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs565785766	chr3:97918825-97918826	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs150227664	chr3:97918852-97918853	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs12490755	chr3:97918853-97918854	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs62267814	chr3:97918860-97918861	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs536599867	chr3:97918870-97918871	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs182233686	chr3:97918879-97918880	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs12498051	chr3:97918883-97918884	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs542404946	chr3:97918910-97918911	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs562286741	chr3:97918914-97918915	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs187487701	chr3:97918924-97918925	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs541658862	chr3:97918931-97918932	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs564742505	chr3:97918940-97918941	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs12489167	chr3:97918947-97918948	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs191521251	chr3:97918954-97918955	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs367758671	chr3:97918973-97918974	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs529388786	chr3:97918978-97918979	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs371240730	chr3:97918994-97918995	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs549241134	chr3:97919007-97919008	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs565853914	chr3:97919014-97919015	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:54)

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
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:95 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:97917800-97918600	Enhancers	ES-WA7 Cell Line	embryonic stem cell
2	chr3:97917800-97927600	Weak transcription	HUES6 Cell Line	embryonic stem cell
3	chr3:97923600-97927600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
4	chr3:97926400-97926600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
5	chr3:97926600-97927600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
6	chr3:97927600-97927800	Enhancers	HUES6 Cell Line	embryonic stem cell
7	chr3:97927600-97928200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
8	chr3:97927600-97928400	Enhancers	HUES64 Cell Line	embryonic stem cell
9	chr3:97927600-97928800	Enhancers	ES-I3 Cell Line	embryonic stem cell
10	chr3:97927600-97928800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
11	chr3:97927800-97928200	Enhancers	iPS-18 Cell Line	embryonic stem cell
12	chr3:97928200-97928400	Enhancers	HUES48 Cell Line	embryonic stem cell
13	chr3:97928200-97932200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
14	chr3:97928200-97936800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
15	chr3:97928400-97932200	Weak transcription	HUES64 Cell Line	embryonic stem cell
16	chr3:97928800-97931000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
17	chr3:97928800-97934000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
18	chr3:97930000-97932000	Weak transcription	HUES48 Cell Line	embryonic stem cell
19	chr3:97931000-97932800	Enhancers	ES-I3 Cell Line	embryonic stem cell
20	chr3:97931800-97932000	Enhancers	iPS-20b Cell Line	embryonic stem cell
21	chr3:97932000-97932200	Active TSS	H1 Cell Line	embryonic stem cell
22	chr3:97932000-97932200	Enhancers	HUES48 Cell Line	embryonic stem cell
23	chr3:97932000-97932800	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
24	chr3:97932200-97932600	Flanking Active TSS	H1 Cell Line	embryonic stem cell
25	chr3:97932200-97932600	Active TSS	H9 Cell Line	embryonic stem cell
26	chr3:97932200-97932600	Flanking Active TSS	HUES64 Cell Line	embryonic stem cell
27	chr3:97932200-97932600	Enhancers	iPS-18 Cell Line	embryonic stem cell
28	chr3:97932200-97932800	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
29	chr3:97932600-97932800	Enhancers	H1 Cell Line	embryonic stem cell
30	chr3:97932600-97932800	Enhancers	HUES6 Cell Line	embryonic stem cell
31	chr3:97932600-97933800	Enhancers	HUES64 Cell Line	embryonic stem cell
32	chr3:97932800-97933600	Enhancers	HUES48 Cell Line	embryonic stem cell
33	chr3:97932800-97933800	Weak transcription	H1 Cell Line	embryonic stem cell
34	chr3:97932800-97936200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
35	chr3:97933800-97934000	Enhancers	H1 Cell Line	embryonic stem cell
36	chr3:97933800-97934200	Enhancers	Primary hematopoietic stem cells short term culture	blood
37	chr3:97933800-97938000	Weak transcription	HUES64 Cell Line	embryonic stem cell
38	chr3:97934000-97934400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
39	chr3:97936200-97936800	Enhancers	ES-I3 Cell Line	embryonic stem cell
40	chr3:97936800-97937600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
41	chr3:97936800-97937800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
42	chr3:97937600-97938000	Enhancers	ES-I3 Cell Line	embryonic stem cell
43	chr3:97937800-97942400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
44	chr3:97938000-97938200	Enhancers	HUES64 Cell Line	embryonic stem cell
45	chr3:97942400-97943400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
46	chr3:97943400-97944000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
47	chr3:97944000-97944200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
48	chr3:97945200-97945600	Active TSS	Esophagus	oesophagus
49	chr3:97951200-97952800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
50	chr3:97951400-97952200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--

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