Variant report

Variant	nsv877619
Chromosome Location	chr3:146106142-146172109
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:233)
CpG islands
(count:244)
Chromatin interactive
region (count:21)
LncRNA
region (count:9)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:233 , 50 per page) page: 1 2 3 4 5

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CBX3	chr3:146130211-146130634	K562	blood:	n/a	n/a
2	CBX3	chr3:146130261-146130561	K562	blood:	n/a	n/a
3	CBX3	chr3:146121518-146121906	HCT-116	colon:	n/a	n/a
4	CBX3	chr3:146163490-146163843	HCT-116	colon:	n/a	n/a
5	CEBPB	chr3:146139507-146139992	MCF-7	breast:	n/a	n/a
6	CEBPB	chr3:146108873-146109145	IMR90	lung:	n/a	n/a
7	CEBPB	chr3:146113046-146113339	A549	lung:	n/a	chr3:146113140-146113151
8	CEBPB	chr3:146139531-146140133	A549	lung:	n/a	n/a
9	CEBPB	chr3:146112954-146113374	K562	blood:	n/a	chr3:146113140-146113151
10	CEBPB	chr3:146112976-146113336	Hela-S3	cervix:	n/a	chr3:146113140-146113151
11	CEBPB	chr3:146112962-146113334	HepG2	liver:	n/a	chr3:146113140-146113151
12	CEBPB	chr3:146140168-146140455	Hela-S3	cervix:	n/a	n/a
13	CEBPB	chr3:146112894-146113347	A549	lung:	n/a	chr3:146113140-146113151
14	CEBPB	chr3:146140161-146140507	MCF-7	breast:	n/a	n/a
15	CEBPB	chr3:146113007-146113331	A549	lung:	n/a	chr3:146113140-146113151
16	CEBPB	chr3:146112957-146113329	IMR90	lung:	n/a	chr3:146113140-146113151
17	CEBPB	chr3:146112955-146113338	H1-hESC	embryonic stem cell:	n/a	chr3:146113140-146113151
18	CEBPB	chr3:146120425-146120469	A549	lung:	n/a	n/a
19	CEBPB	chr3:146113057-146113226	ECC-1	luminal epithelium:	n/a	chr3:146113140-146113151
20	CHD2	chr3:146145207-146145271	Hela-S3	cervix:	n/a	n/a
21	CTCF	chr3:146121080-146121230	GM12874	blood:	n/a	n/a
22	CTCF	chr3:146140260-146140410	AoAF	blood vessel:	n/a	n/a
23	CTCF	chr3:146140300-146140450	HPF	lung:	n/a	n/a
24	CTCF	chr3:146140359-146140445	LNCaP	prostate:	n/a	n/a
25	CTCF	chr3:146140293-146140462	Hela-S3	cervix:	n/a	n/a
26	CTCF	chr3:146140261-146140470	MCF-7	breast:	n/a	n/a
27	CTCF	chr3:146140340-146140490	HA-sp	spinal cord:	n/a	n/a
28	CTCF	chr3:146128646-146128786	K562	blood:	n/a	n/a
29	CTCF	chr3:146136520-146136670	MCF-7	breast:	n/a	n/a
30	CTCF	chr3:146140340-146140490	A549	lung:	n/a	n/a
31	CTCF	chr3:146140300-146140450	A549	lung:	n/a	n/a
32	CTCF	chr3:146140280-146140430	HCPEpiC	choroid plexus:	n/a	n/a
33	CTCF	chr3:146140340-146140490	HMF	breast:	n/a	n/a
34	CTCF	chr3:146130691-146130720	Kidney_OC	kidney:	n/a	n/a
35	CTCF	chr3:146167520-146167670	MCF-7	breast:	n/a	n/a
36	CTCF	chr3:146140280-146140430	MCF-7	breast:	n/a	n/a
37	CTCF	chr3:146140905-146141193	IMR90	lung:	n/a	n/a
38	CTCF	chr3:146114180-146114330	HCM	heart:	n/a	n/a
39	CTCF	chr3:146158363-146158401	Fibrobl	skin:	n/a	n/a
40	CTCF	chr3:146140300-146140450	MCF-7	breast:	n/a	n/a
41	CTCF	chr3:146140216-146140572	MCF-7	breast:	n/a	n/a
42	CTCF	chr3:146167520-146167670	HCPEpiC	choroid plexus:	n/a	n/a
43	CTCF	chr3:146140240-146140390	HMF	breast:	n/a	n/a
44	CTCF	chr3:146140256-146140481	MCF-7	breast:	n/a	n/a
45	CTCF	chr3:146140289-146140439	LNCaP	prostate:	n/a	n/a
46	CTCF	chr3:146126503-146126564	K562	blood:	n/a	n/a
47	CTCF	chr3:146140920-146141070	BJ	skin:	n/a	n/a
48	CTCF	chr3:146128660-146128810	HepG2	liver:	n/a	n/a
49	CTCF	chr3:146128722-146128814	K562	blood:	n/a	n/a
50	CTCF	chr3:146140300-146140450	NHEK	skin:	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	chr3:146157056-146157106	H1-hESC	embryonic stem cell:	embryo
2	chr3:146129420-146129470	PANC-1	pancreas:	n/a
3	chr3:146129420-146129470	HEK293	kidney:	embryo
4	chr3:146129420-146129470	HCT-116	colon:	n/a
5	chr3:146129264-146129314	HCM	heart:	n/a
6	chr3:146129420-146129470	BJ	skin:	n/a
7	chr3:146129264-146129314	GM06990	blood:	n/a
8	chr3:146129420-146129470	K562	blood:	n/a
9	chr3:146129420-146129470	HL-60	blood:	n/a
10	chr3:146129360-146129410	HNPCEpiC	eye:	n/a
11	chr3:146129264-146129314	ProgFib	skin:	n/a
12	chr3:146129360-146129410	ECC-1	luminal epithelium:	n/a
13	chr3:146157056-146157106	Caco-2	colon:	n/a
14	chr3:146129420-146129470	AG04449	skin:	fetal
15	chr3:146157056-146157106	HCT-116	colon:	n/a
16	chr3:146129420-146129470	HCM	heart:	n/a
17	chr3:146129360-146129410	GM12891	blood:	n/a
18	chr3:146157056-146157106	MCF10A-Er-Src	breast:	n/a
19	chr3:146129264-146129314	SKMC	muscle:	n/a
20	chr3:146157056-146157106	IMR90	lung:	fetal
21	chr3:146129420-146129470	Jurkat	blood:	n/a
22	chr3:146157056-146157106	NHBE	bronchial:	n/a
23	chr3:146129360-146129410	CMK	blood:	n/a
24	chr3:146129420-146129470	PFSK-1	brain:	n/a
25	chr3:146157056-146157106	RPTEC	kidney:	n/a
26	chr3:146157056-146157106	Hepatocyte	liver:	n/a
27	chr3:146129264-146129314	U87	brain:	n/a
28	chr3:146129420-146129470	AG10803	skin:	n/a
29	chr3:146129420-146129470	NHBE	bronchial:	n/a
30	chr3:146129360-146129410	SAEC	small airway:	n/a
31	chr3:146129420-146129470	AG04450	lung:	fetal
32	chr3:146157056-146157106	A549	lung:	n/a
33	chr3:146129264-146129314	H1-hESC	embryonic stem cell:	embryo
34	chr3:146157056-146157106	HepG2	liver:	n/a
35	chr3:146129264-146129314	AG04449	skin:	fetal
36	chr3:146129420-146129470	HRPEpiC	eye:	n/a
37	chr3:146129420-146129470	AG09319	gingival:	n/a
38	chr3:146129360-146129410	AoSMC	blood vessel:	n/a
39	chr3:146129264-146129314	AG09309	skin:	n/a
40	chr3:146129420-146129470	SK-N-SH	brain:	n/a
41	chr3:146129420-146129470	HPAEpiC	pulmonary alveolar:	n/a
42	chr3:146129360-146129410	BE2_C	brain:	n/a
43	chr3:146129420-146129470	Hela-S3	cervix:	n/a
44	chr3:146129360-146129410	AG10803	skin:	n/a
45	chr3:146157056-146157106	PFSK-1	brain:	n/a
46	chr3:146129360-146129410	SK-N-SH_RA	brain:	n/a
47	chr3:146157056-146157106	T-47D	breast:	n/a
48	chr3:146129360-146129410	AG04450	lung:	fetal
49	chr3:146157056-146157106	GM12891	blood:	n/a
50	chr3:146129420-146129470	AoSMC	blood vessel:	n/a

(count:21 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr3:146158561..146161277-chr3:146161473..146163225,2	K562	blood:
2	chr3:146139609..146141816-chr3:146146728..146148840,3	MCF-7	breast:
3	chr3:146155934..146158732-chr3:146162320..146163882,2	MCF-7	breast:
4	chr3:146137722..146139477-chr3:146142959..146145248,2	MCF-7	breast:
5	chr3:146139398..146141443-chr3:146220518..146223634,3	MCF-7	breast:
6	chr3:146137952..146139503-chr3:146261134..146263708,2	MCF-7	breast:
7	chr3:146158889..146161569-chr3:146161974..146164517,2	MCF-7	breast:
8	chr3:146133340..146136821-chr3:146137357..146140210,3	MCF-7	breast:
9	chr3:146137722..146139477-chr3:146142959..146145248,2	MCF-7	breast:
10	chr3:146139609..146141816-chr3:146146728..146148840,3	MCF-7	breast:
11	chr3:146158561..146161277-chr3:146161473..146163225,2	K562	blood:
12	chr3:146169890..146171748-chr3:146177366..146178910,2	K562	blood:
13	chr3:146168876..146171592-chr3:146171883..146173684,2	K562	blood:
14	chr3:146168876..146171592-chr3:146171883..146173684,2	K562	blood:
15	chr3:146051931..146052494-chr3:146139879..146140654,2	MCF-7	breast:
16	chr3:146155934..146158732-chr3:146162320..146163882,2	MCF-7	breast:
17	chr3:146142625..146144505-chr3:146147964..146150004,2	K562	blood:
18	chr3:146158889..146161569-chr3:146161974..146164517,2	MCF-7	breast:
19	chr3:146139318..146141303-chr3:146183434..146185764,2	MCF-7	breast:
20	chr3:145879440..145881243-chr3:146138706..146140785,2	MCF-7	breast:
21	chr3:146142625..146144505-chr3:146147964..146150004,2	K562	blood:

(count:9 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PLSCR2-1	chr3:146116444-146116610	NONHSAT092557
2	lnc-PLSCR2-1	chr3:146109150-146109349	NONHSAT092556
3	lnc-PLSCR2-1	chr3:146113547-146113708	NONHSAT092556
4	lnc-PLSCR2-1	chr3:146132912-146132954	NONHSAT092556
5	lnc-PLSCR2-1	chr3:146113527-146113702	NONHSAT092557
6	lnc-PLSCR2-1	chr3:146134291-146134390	NONHSAT092556
7	lnc-PLSCR2-1	chr3:146119147-146119346	NONHSAT092556
8	lnc-PLSCR2-1	chr3:146119142-146119363	NONHSAT092557
9	lnc-PLSCR2-1	chr3:146134293-146134364	NONHSAT092557

No data

Variant related genes	Relation type
ENSG00000241358	TF binding region
ENSG00000241358	CpG island
ENSG00000188313	chromatin interactions
ENSG00000241358	chromatin interactions
ENSG00000163746	chromatin interactions

Extended variants
information (count: 2180 )
Associated
traits (count: 54 )

Variant overlapped rSNPs/rCNVs (count:2180 , 50 per page) page: 1 2 3 4 5 6 7 ... 44

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2867865	chr3:146106142-146106143	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs79814442	chr3:146106177-146106178	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs183915975	chr3:146106186-146106187	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs546361065	chr3:146106187-146106188	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs572564572	chr3:146106210-146106211	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs564453616	chr3:146106211-146106212	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs531831483	chr3:146106231-146106232	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs142962998	chr3:146106285-146106286	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs112586515	chr3:146106295-146106296	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs540316018	chr3:146106298-146106299	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs144683281	chr3:146106312-146106313	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs547261490	chr3:146106391-146106392	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs58038409	chr3:146106404-146106405	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs539291265	chr3:146106414-146106415	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs551550151	chr3:146106435-146106436	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs148573917	chr3:146106438-146106439	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs142974062	chr3:146106449-146106450	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs113397096	chr3:146106476-146106477	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs188252963	chr3:146106557-146106558	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs564879671	chr3:146106562-146106563	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs536999370	chr3:146106589-146106590	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs536170172	chr3:146106615-146106616	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs554200032	chr3:146106640-146106641	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs180753720	chr3:146106654-146106655	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs150703627	chr3:146106662-146106663	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs368821640	chr3:146106698-146106699	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs564696300	chr3:146106731-146106732	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs576141027	chr3:146106754-146106755	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs80095434	chr3:146106769-146106770	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs140122908	chr3:146106833-146106834	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs143831262	chr3:146106876-146106877	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs371076436	chr3:146106878-146106879	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs537217542	chr3:146106919-146106920	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs146446241	chr3:146106983-146106984	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs551296271	chr3:146107005-146107006	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs187437819	chr3:146107027-146107028	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs190211757	chr3:146107064-146107065	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs549062295	chr3:146107078-146107079	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs374176738	chr3:146107112-146107113	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs567352819	chr3:146107149-146107150	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs534628287	chr3:146107198-146107199	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs552932652	chr3:146107213-146107214	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
43	rs566286249	chr3:146107309-146107310	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
44	rs540088469	chr3:146107320-146107321	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
45	rs557532091	chr3:146107367-146107368	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
46	rs182392837	chr3:146107423-146107424	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs576203351	chr3:146107428-146107429	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs543525703	chr3:146107511-146107512	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs143114197	chr3:146107557-146107558	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs372112288	chr3:146107579-146107580	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:54)

Disease	PMID	Source
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Glioblastoma multiforme	21080181	CNVD
Retinoblastoma	21504564	CNVD
Medulloblastoma	21979893	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
Squamous cell cancer	20885788	CNVD
Melanoma	18172304	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Bipolar disorder	18458673	CNVD
Breast cancer	22032731	CNVD
Breast cancer	16461572	CNVD
Neuroblastoma	17533364	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
Chronic lymphocytic leukemia	21546498	CNVD
Basal cell lymphoma	21115979	CNVD
Colorectal cancer	18645599	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Hepatocellular carcinoma	16750200	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Myelodysplastic syndrome	21251322	CNVD
Blepharophimosis-ptosis-epicanthus inversus syndrome	22067867	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
abnormal development	18461090	CNVD
Breast cancer	21364760	CNVD
Mental retardation	17847001	CNVD
Basal cell lymphoma	17170743	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Autism	18923514	CNVD
Autism	22241247	CNVD
Myelofibrosis	22110671	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Autism	21956041	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Breast cancer	16608533	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Breast cancer	21509527	CNVD

Chromatin state (count:146 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:146100800-146112600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr3:146101600-146111800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
3	chr3:146104800-146106800	Enhancers	A549	lung
4	chr3:146105400-146106200	Enhancers	Fetal Lung	lung
5	chr3:146106000-146106200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
6	chr3:146106000-146106200	Enhancers	Ovary	ovary
7	chr3:146106200-146107200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
8	chr3:146106200-146107200	Weak transcription	Fetal Lung	lung
9	chr3:146106200-146107200	Weak transcription	Ovary	ovary
10	chr3:146106800-146107200	Weak transcription	A549	lung
11	chr3:146107200-146107400	Enhancers	Ovary	ovary
12	chr3:146107200-146107400	Bivalent Enhancer	Sigmoid Colon	Sigmoid Colon
13	chr3:146107200-146108800	Enhancers	Fetal Stomach	stomach
14	chr3:146107200-146109600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
15	chr3:146107200-146110000	Enhancers	Fetal Lung	lung
16	chr3:146107600-146108600	Weak transcription	Sigmoid Colon	Sigmoid Colon
17	chr3:146107800-146108400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
18	chr3:146108000-146109400	Enhancers	Muscle Satellite Cultured Cells	--
19	chr3:146108000-146109600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
20	chr3:146108000-146109600	Enhancers	Osteobl	bone
21	chr3:146108200-146108400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
22	chr3:146108200-146108600	Enhancers	Colon Smooth Muscle	Colon
23	chr3:146108400-146108800	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
24	chr3:146108400-146108800	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
25	chr3:146108400-146108800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
26	chr3:146108400-146109000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
27	chr3:146108400-146109000	Enhancers	NHLF	lung
28	chr3:146108400-146109200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
29	chr3:146108400-146109200	Enhancers	NH-A	brain
30	chr3:146108600-146109000	Enhancers	Brain Germinal Matrix	brain
31	chr3:146108600-146109000	Enhancers	Sigmoid Colon	Sigmoid Colon
32	chr3:146108600-146109200	Enhancers	Adipose Nuclei	Adipose
33	chr3:146108600-146109200	Enhancers	Small Intestine	intestine
34	chr3:146108600-146109200	Enhancers	NHDF-Ad	bronchial
35	chr3:146108800-146109000	Enhancers	A549	lung
36	chr3:146108800-146109600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
37	chr3:146108800-146109600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
38	chr3:146109600-146113200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
39	chr3:146110000-146114600	Weak transcription	Fetal Lung	lung
40	chr3:146111800-146119400	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
41	chr3:146112600-146112800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
42	chr3:146113200-146113600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
43	chr3:146114000-146115600	Enhancers	HUVEC	blood vessel
44	chr3:146114200-146115400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
45	chr3:146114400-146115400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
46	chr3:146114600-146115000	Enhancers	Primary hematopoietic stem cells short term culture	blood
47	chr3:146114600-146115400	Enhancers	Fetal Lung	lung
48	chr3:146118800-146119200	Enhancers	iPS-15b Cell Line	embryonic stem cell
49	chr3:146119200-146119400	Enhancers	iPS-20b Cell Line	embryonic stem cell
50	chr3:146119200-146121200	Weak transcription	iPS-15b Cell Line	embryonic stem cell

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