Variant report

Variant	nsv2693
Chromosome Location	chr2:39468641-39513800
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:254)
CpG islands
(count:549)
Chromatin interactive
region (count:20)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:254 , 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	chr2:39475252-39475385	HepG2	liver:	n/a	n/a
2	BATF	chr2:39493258-39493611	GM12878	blood:	n/a	chr2:39493418-39493429
3	BHLHE40	chr2:39492072-39492073	GM12878	blood:	n/a	n/a
4	CEBPB	chr2:39493515-39493518	A549	lung:	n/a	n/a
5	CHD1	chr2:39504205-39504287	H1-hESC	embryonic stem cell:	n/a	n/a
6	CHD1	chr2:39492022-39492064	GM12878	blood:	n/a	n/a
7	CTCF	chr2:39504320-39504470	HMF	breast:	n/a	n/a
8	CTCF	chr2:39475180-39475330	HUVEC	blood vessel:	n/a	n/a
9	CTCF	chr2:39472300-39472450	GM12873	blood:	n/a	n/a
10	CTCF	chr2:39495936-39495942	GM10266	blood:	n/a	n/a
11	CTCF	chr2:39475160-39475310	GM12872	blood:	n/a	n/a
12	CTCF	chr2:39470920-39471070	GM12869	blood:	n/a	n/a
13	CTCF	chr2:39475227-39475320	Hela-S3	cervix:	n/a	n/a
14	CTCF	chr2:39498782-39498847	A549	lung:	n/a	n/a
15	CTCF	chr2:39472280-39472430	NB4	blood:	n/a	n/a
16	CTCF	chr2:39469283-39469287	A549	lung:	n/a	n/a
17	CTCF	chr2:39504320-39504470	A549	lung:	n/a	n/a
18	CTCF	chr2:39472260-39472410	BJ	skin:	n/a	n/a
19	CTCF	chr2:39513386-39513486	ProgFib	skin:	n/a	n/a
20	CTCF	chr2:39513395-39513490	MCF-7	breast:	n/a	n/a
21	CTCF	chr2:39472338-39472487	GM12892	blood:	n/a	n/a
22	CTCF	chr2:39472356-39472477	GM13976	blood:	n/a	n/a
23	CTCF	chr2:39471020-39471170	SK-N-SH_RA	brain:	n/a	n/a
24	CTCF	chr2:39499960-39500110	HepG2	liver:	n/a	n/a
25	CTCF	chr2:39513376-39513504	MCF-7	breast:	n/a	n/a
26	CTCF	chr2:39509144-39509225	Medullo	brain:	n/a	n/a
27	CTCF	chr2:39472300-39472450	GM12871	blood:	n/a	n/a
28	CTCF	chr2:39475180-39475330	HPAF	blood vessel:	n/a	n/a
29	CTCF	chr2:39513342-39513483	MCF-7	breast:	n/a	n/a
30	CTCF	chr2:39495001-39495050	K562	blood:	n/a	n/a
31	CTCF	chr2:39471720-39471870	SK-N-SH_RA	brain:	n/a	n/a
32	CTCF	chr2:39513404-39513466	H1-hESC	embryonic stem cell:	n/a	n/a
33	CTCF	chr2:39472280-39472430	HL-60	blood:	n/a	n/a
34	CTCF	chr2:39513396-39513468	A549	lung:	n/a	n/a
35	CTCF	chr2:39472386-39472475	GM19239	blood:	n/a	n/a
36	CTCF	chr2:39493280-39493430	GM12873	blood:	n/a	n/a
37	CTCF	chr2:39470940-39471090	SK-N-SH_RA	brain:	n/a	n/a
38	CUX1	chr2:39493289-39493480	GM12878	blood:	n/a	n/a
39	E2F4	chr2:39489319-39489603	MCF10A-Er-Src	breast:	n/a	n/a
40	EBF1	chr2:39493298-39493504	GM12878	blood:	n/a	n/a
41	EBF1	chr2:39510813-39511037	GM12878	blood:	n/a	chr2:39510906-39510917 chr2:39510921-39510932
42	EBF1	chr2:39470974-39471218	GM12878	blood:	n/a	n/a
43	EBF1	chr2:39493194-39493552	GM12878	blood:	n/a	n/a
44	EBF1	chr2:39493164-39493524	GM12878	blood:	n/a	n/a
45	EBF1	chr2:39491382-39491410	GM12878	blood:	n/a	n/a
46	EP300	chr2:39491289-39491435	GM12878	blood:	n/a	chr2:39491334-39491348
47	EP300	chr2:39493273-39493470	GM12878	blood:	n/a	n/a
48	EP300	chr2:39491401-39491446	GM12878	blood:	n/a	n/a
49	FOS	chr2:39493630-39493827	MCF10A-Er-Src	breast:	n/a	chr2:39493800-39493807 chr2:39493799-39493808 chr2:39493801-39493812 chr2:39493800-39493808
50	FOS	chr2:39502191-39502509	MCF10A-Er-Src	breast:	n/a	n/a

(count:549 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:39472197-39472247	Hela-S3	cervix:	n/a
2	chr2:39471182-39471232	AG10803	skin:	n/a
3	chr2:39475086-39475136	AG04449	skin:	fetal
4	chr2:39471028-39471078	HRPEpiC	eye:	n/a
5	chr2:39471028-39471078	CMK	blood:	n/a
6	chr2:39475086-39475136	NT2-D1	testis:	n/a
7	chr2:39493603-39493653	GM06990	blood:	n/a
8	chr2:39472197-39472247	GM19239	blood:	n/a
9	chr2:39472684-39472734	AG04449	skin:	fetal
10	chr2:39472197-39472247	AG09319	gingival:	n/a
11	chr2:39471182-39471232	AG09319	gingival:	n/a
12	chr2:39470725-39470775	HCM	heart:	n/a
13	chr2:39470743-39470793	SKMC	muscle:	n/a
14	chr2:39493603-39493653	HRPEpiC	eye:	n/a
15	chr2:39470743-39470793	HNPCEpiC	eye:	n/a
16	chr2:39471182-39471232	HRPEpiC	eye:	n/a
17	chr2:39471182-39471232	Caco-2	colon:	n/a
18	chr2:39471182-39471232	HIPEpiC	eye:	n/a
19	chr2:39472197-39472247	SK-N-SH	brain:	n/a
20	chr2:39475086-39475136	HPAEpiC	pulmonary alveolar:	n/a
21	chr2:39471182-39471232	HEK293	kidney:	embryo
22	chr2:39472197-39472247	ProgFib	skin:	n/a
23	chr2:39470743-39470793	U87	brain:	n/a
24	chr2:39475086-39475136	BJ	skin:	n/a
25	chr2:39470743-39470793	HMEC	breast:	n/a
26	chr2:39471182-39471232	AG04450	lung:	fetal
27	chr2:39493603-39493653	HIPEpiC	eye:	n/a
28	chr2:39470725-39470775	ECC-1	luminal epithelium:	n/a
29	chr2:39475086-39475136	NB4	blood:	n/a
30	chr2:39475086-39475136	A549	lung:	n/a
31	chr2:39470743-39470793	HCT-116	colon:	n/a
32	chr2:39470750-39470800	MCF-7	breast:	n/a
33	chr2:39471028-39471078	RPTEC	kidney:	n/a
34	chr2:39470725-39470775	HL-60	blood:	n/a
35	chr2:39470725-39470775	HIPEpiC	eye:	n/a
36	chr2:39471028-39471078	Hepatocyte	liver:	n/a
37	chr2:39470725-39470775	HAEpiC	amniotic membrane:	n/a
38	chr2:39472684-39472734	Hela-S3	cervix:	n/a
39	chr2:39470725-39470775	PrEC	prostate:	n/a
40	chr2:39470750-39470800	IMR90	lung:	fetal
41	chr2:39475086-39475136	ECC-1	luminal epithelium:	n/a
42	chr2:39470743-39470793	GM12891	blood:	n/a
43	chr2:39472684-39472734	PANC-1	pancreas:	n/a
44	chr2:39470725-39470775	RPTEC	kidney:	n/a
45	chr2:39470743-39470793	AG10803	skin:	n/a
46	chr2:39470743-39470793	MCF-7	breast:	n/a
47	chr2:39493603-39493653	AG09319	gingival:	n/a
48	chr2:39470750-39470800	BE2_C	brain:	n/a
49	chr2:39472684-39472734	AG10803	skin:	n/a
50	chr2:39471182-39471232	HNPCEpiC	eye:	n/a

(count:20 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:39490995..39493794-chr2:39495082..39499421,5	K562	blood:
2	chr2:39460764..39463142-chr2:39468024..39469641,2	K562	blood:
3	chr2:39468106..39472763-chr2:39473661..39477001,5	MCF-7	breast:
4	chr2:39476438..39480963-chr2:39481034..39484561,4	K562	blood:
5	chr2:39489136..39490655-chr2:39494210..39497075,2	K562	blood:
6	chr2:39476438..39480963-chr2:39481034..39484561,4	K562	blood:
7	chr2:39468106..39472763-chr2:39473661..39477001,5	MCF-7	breast:
8	chr2:39499119..39502094-chr2:39503052..39505530,2	K562	blood:
9	chr2:39498139..39500783-chr2:39514401..39516226,2	K562	blood:
10	chr2:39476355..39478295-chr2:39480403..39482715,2	MCF-7	breast:
11	chr2:39483897..39486099-chr2:39504200..39506352,2	K562	blood:
12	chr2:39496358..39498173-chr2:39503458..39507219,3	K562	blood:
13	chr2:39506271..39508619-chr2:39510238..39511844,2	K562	blood:
14	chr2:39476355..39478295-chr2:39480403..39482715,2	MCF-7	breast:
15	chr2:39484279..39485806-chr2:39491363..39493420,2	MCF-7	breast:
16	chr2:39499119..39502094-chr2:39503052..39505530,2	K562	blood:
17	chr2:39490995..39493794-chr2:39495082..39499421,5	K562	blood:
18	chr17:73408437..73408956-chr2:39475634..39476134,2	MCF-7	breast:
19	chr2:39484279..39485806-chr2:39491363..39493420,2	MCF-7	breast:
20	chr2:39508670..39510493-chr2:39518099..39520672,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-MAP4K3-1	chr2:39472055-39472707	NONHSAT070223
2	lnc-CDKL4-3	chr2:39511169-39511421	expReg_chr2_3022_-
3	lnc-MAP4K3-1	chr2:39473220-39473335	NONHSAT070223

No data

Variant related genes	Relation type
MAP4K3	TF binding region
ENSG00000252473	TF binding region
MAP4K3	CpG island
ENSG00000252473	CpG island
ENSG00000252473	chromatin interactions
ENSG00000011566	chromatin interactions

Extended variants
information (count: 1908 )
Associated
traits (count: 61 )

Variant overlapped rSNPs/rCNVs (count:1908 , 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	rs557901755	chr2:39468647-39468648	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs569889220	chr2:39468673-39468674	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs4516411	chr2:39468676-39468677	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs374475724	chr2:39468705-39468706	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs191860689	chr2:39468710-39468711	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs542268719	chr2:39468713-39468714	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs554154731	chr2:39468721-39468722	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs184412759	chr2:39468728-39468729	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs11900474	chr2:39468760-39468761	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs142862664	chr2:39468791-39468792	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs531798358	chr2:39468836-39468837	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs188422056	chr2:39468839-39468840	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs193205187	chr2:39468840-39468841	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs528837702	chr2:39468865-39468866	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs547406346	chr2:39468888-39468889	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs565558677	chr2:39468908-39468909	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs145078116	chr2:39468962-39468963	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs537362300	chr2:39468981-39468982	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs539917660	chr2:39469072-39469073	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs111760328	chr2:39469102-39469103	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs185536552	chr2:39469128-39469129	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs537286987	chr2:39469147-39469148	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs550273601	chr2:39469149-39469150	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs370246608	chr2:39469160-39469161	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs373750797	chr2:39469167-39469168	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs74579526	chr2:39469199-39469200	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs554106981	chr2:39469200-39469201	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs558317629	chr2:39469206-39469207	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs138666548	chr2:39469218-39469219	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs540086502	chr2:39469255-39469256	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs558208252	chr2:39469283-39469284	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs576227321	chr2:39469314-39469315	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs78333931	chr2:39469398-39469399	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs116154416	chr2:39469447-39469448	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs190786014	chr2:39469473-39469474	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs566867347	chr2:39469519-39469520	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs573370426	chr2:39469520-39469521	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs540792807	chr2:39469599-39469600	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs180797523	chr2:39469679-39469680	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs115212443	chr2:39469698-39469699	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs551648486	chr2:39469715-39469716	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs116749806	chr2:39469727-39469728	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs114058533	chr2:39469732-39469733	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs373665626	chr2:39469745-39469746	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs567490559	chr2:39469767-39469768	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs141777478	chr2:39469782-39469783	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs150788912	chr2:39469814-39469815	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs13412798	chr2:39469819-39469820	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs566056305	chr2:39469847-39469848	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs113266533	chr2:39469884-39469885	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:61)

Disease	PMID	Source
Breast cancer	17393978	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Breast cancer	17603634	CNVD
Medulloblastoma	21979893	CNVD
Lynch syndrome	18415027	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Diffuse large b-cell lymphoma	18287131	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
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Ependymoma	16718352	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
lymphocytic leukemia	21291569	CNVD
Prostate cancer	18632612	CNVD
Bladder cancer	21909424	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Follicular lymphoma	20505157	CNVD
Autism	17483303	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Medulloblastoma	20607354	CNVD
Leukemia	18628472	CNVD
Autism	22495311	CNVD
Autism	19521722	CNVD
Autism	18522746	CNVD
Non-small cell lung cancer	18927303	CNVD
Breast cancer	21785460	CNVD
Lung cancer	18438408	CNVD
Prostate cancer	21965145	CNVD
Breast cancer	16397240	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	21508638	CNVD
Neurodevelopmental disorder	22521361	CNVD
Neurocytoma	17123091	CNVD
small cell lung cancer	20016488	CNVD
Melanoma	18172304	CNVD
Cancer	16751803	CNVD
Breast cancer	21364760	CNVD
Colorectal cancer	16272173	CNVD
Breast cancer	22522925	CNVD
T-cell lymphomas	22341440	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:1397 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:39423400-39470800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr2:39449200-39477600	Weak transcription	HSMMtube	muscle
3	chr2:39455400-39470600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr2:39455800-39472200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
5	chr2:39456000-39472000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
6	chr2:39456200-39475600	Weak transcription	NHDF-Ad	bronchial
7	chr2:39460800-39468800	Weak transcription	H1 Cell Line	embryonic stem cell
8	chr2:39464400-39474600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
9	chr2:39466800-39470800	Weak transcription	Osteobl	bone
10	chr2:39468000-39469200	Enhancers	ES-I3 Cell Line	embryonic stem cell
11	chr2:39468000-39469200	Enhancers	Primary T regulatory cells fromperipheralblood	blood
12	chr2:39468200-39469200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr2:39468200-39469200	Enhancers	iPS-20b Cell Line	embryonic stem cell
14	chr2:39468200-39470200	Enhancers	HepG2	liver
15	chr2:39468400-39469200	Enhancers	HUES48 Cell Line	embryonic stem cell
16	chr2:39468400-39469200	Enhancers	HUES64 Cell Line	embryonic stem cell
17	chr2:39468400-39469200	Enhancers	iPS-15b Cell Line	embryonic stem cell
18	chr2:39468400-39469600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
19	chr2:39468400-39470600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
20	chr2:39468600-39469200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
21	chr2:39468600-39469600	Enhancers	HUES6 Cell Line	embryonic stem cell
22	chr2:39468600-39469600	Enhancers	iPS-18 Cell Line	embryonic stem cell
23	chr2:39468600-39469600	Enhancers	HUVEC	blood vessel
24	chr2:39468800-39469000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
25	chr2:39468800-39469000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
26	chr2:39468800-39469000	Enhancers	Fetal Heart	heart
27	chr2:39468800-39469400	Enhancers	H1 Cell Line	embryonic stem cell
28	chr2:39468800-39469400	Enhancers	H9 Cell Line	embryonic stem cell
29	chr2:39469000-39474000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
30	chr2:39469000-39475800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
31	chr2:39469200-39469400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
32	chr2:39469200-39469400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
33	chr2:39469200-39469400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
34	chr2:39469200-39469400	Enhancers	Esophagus	oesophagus
35	chr2:39469200-39469400	Enhancers	Lung	lung
36	chr2:39469200-39469600	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
37	chr2:39469200-39469600	Enhancers	Left Ventricle	heart
38	chr2:39469200-39470600	Weak transcription	HUES64 Cell Line	embryonic stem cell
39	chr2:39469200-39473600	Weak transcription	Fetal Heart	heart
40	chr2:39469200-39474800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
41	chr2:39469200-39475800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
42	chr2:39469200-39476400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
43	chr2:39469200-39477400	Weak transcription	HUES48 Cell Line	embryonic stem cell
44	chr2:39469200-39478000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
45	chr2:39469200-39503800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
46	chr2:39469400-39470000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
47	chr2:39469400-39470600	Weak transcription	H1 Cell Line	embryonic stem cell
48	chr2:39469400-39470600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
49	chr2:39469400-39470800	Weak transcription	Esophagus	oesophagus
50	chr2:39469400-39471000	Weak transcription	Lung	lung

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