Variant report

Variant	nsv875377
Chromosome Location	chr2:168084857-168203116
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:168149471-168149640	HepG2	liver:	n/a	n/a
2	ATF2	chr2:168131268-168131939	H1-hESC	embryonic stem cell:	n/a	n/a
3	ATF2	chr2:168188179-168188799	H1-hESC	embryonic stem cell:	n/a	n/a
4	ATF2	chr2:168128467-168128750	H1-hESC	embryonic stem cell:	n/a	n/a
5	ATF3	chr2:168149455-168149778	HepG2	liver:	n/a	n/a
6	BACH1	chr2:168149948-168150336	H1-hESC	embryonic stem cell:	n/a	n/a
7	BACH1	chr2:168148879-168149186	H1-hESC	embryonic stem cell:	n/a	n/a
8	BACH1	chr2:168150899-168151418	H1-hESC	embryonic stem cell:	n/a	n/a
9	BACH1	chr2:168188139-168188775	H1-hESC	embryonic stem cell:	n/a	n/a
10	BACH1	chr2:168111908-168111943	H1-hESC	embryonic stem cell:	n/a	n/a
11	BCL11A	chr2:168188505-168188763	H1-hESC	embryonic stem cell:	n/a	n/a
12	BCL11A	chr2:168188421-168188765	H1-hESC	embryonic stem cell:	n/a	n/a
13	BRCA1	chr2:168149496-168149582	HepG2	liver:	n/a	n/a
14	BRCA1	chr2:168149381-168149526	H1-hESC	embryonic stem cell:	n/a	n/a
15	CCNT2	chr2:168149524-168149719	K562	blood:	n/a	n/a
16	CEBPB	chr2:168161433-168161634	H1-hESC	embryonic stem cell:	n/a	chr2:168161512-168161523
17	CEBPB	chr2:168174113-168174356	A549	lung:	n/a	chr2:168174210-168174221 chr2:168174286-168174299
18	CEBPB	chr2:168120950-168121196	MCF-7	breast:	n/a	n/a
19	CEBPB	chr2:168088643-168088871	IMR90	lung:	n/a	chr2:168088719-168088728 chr2:168088716-168088733 chr2:168088717-168088728 chr2:168088718-168088729
20	CEBPB	chr2:168105757-168106028	H1-hESC	embryonic stem cell:	n/a	chr2:168105897-168105908
21	CEBPB	chr2:168147705-168148060	IMR90	lung:	n/a	chr2:168147877-168147888 chr2:168147877-168147886 chr2:168147875-168147888 chr2:168147875-168147886 chr2:168147877-168147886 chr2:168147877-168147886 chr2:168147877-168147886
22	CEBPB	chr2:168181901-168182104	HepG2	liver:	n/a	chr2:168181978-168181989
23	CEBPB	chr2:168174066-168174318	IMR90	lung:	n/a	chr2:168174210-168174221 chr2:168174286-168174299
24	CEBPB	chr2:168140879-168141121	H1-hESC	embryonic stem cell:	n/a	n/a
25	CEBPB	chr2:168188214-168188766	H1-hESC	embryonic stem cell:	n/a	n/a
26	CEBPB	chr2:168151083-168151380	H1-hESC	embryonic stem cell:	n/a	n/a
27	CEBPB	chr2:168174048-168174365	HepG2	liver:	n/a	chr2:168174210-168174221 chr2:168174286-168174299
28	CEBPB	chr2:168105746-168106060	IMR90	lung:	n/a	chr2:168105897-168105908
29	CEBPB	chr2:168130867-168131125	H1-hESC	embryonic stem cell:	n/a	chr2:168130925-168130938 chr2:168130925-168130938
30	CEBPB	chr2:168147693-168148254	HepG2	liver:	n/a	chr2:168147877-168147888 chr2:168147877-168147886 chr2:168147875-168147888 chr2:168147875-168147886 chr2:168147877-168147886 chr2:168147877-168147886 chr2:168147877-168147886
31	CEBPB	chr2:168105756-168106072	A549	lung:	n/a	chr2:168105897-168105908
32	CEBPB	chr2:168147788-168148038	A549	lung:	n/a	chr2:168147877-168147888 chr2:168147877-168147886 chr2:168147875-168147888 chr2:168147875-168147886 chr2:168147877-168147886 chr2:168147877-168147886 chr2:168147877-168147886
33	CEBPB	chr2:168149422-168149502	H1-hESC	embryonic stem cell:	n/a	chr2:168149476-168149484
34	CEBPB	chr2:168181934-168182110	A549	lung:	n/a	chr2:168181978-168181989
35	CEBPB	chr2:168161418-168161682	HepG2	liver:	n/a	chr2:168161512-168161523
36	CEBPB	chr2:168201377-168201577	HepG2	liver:	n/a	n/a
37	CEBPB	chr2:168088629-168088894	HepG2	liver:	n/a	chr2:168088719-168088728 chr2:168088716-168088733 chr2:168088717-168088728 chr2:168088718-168088729
38	CEBPB	chr2:168147735-168148005	H1-hESC	embryonic stem cell:	n/a	chr2:168147877-168147888 chr2:168147877-168147886 chr2:168147875-168147888 chr2:168147875-168147886 chr2:168147877-168147886 chr2:168147877-168147886 chr2:168147877-168147886
39	CEBPB	chr2:168105742-168106088	HepG2	liver:	n/a	chr2:168105897-168105908
40	CEBPB	chr2:168147740-168148048	K562	blood:	n/a	chr2:168147877-168147888 chr2:168147877-168147886 chr2:168147875-168147888 chr2:168147875-168147886 chr2:168147877-168147886 chr2:168147877-168147886 chr2:168147877-168147886
41	CHD1	chr2:168149986-168150077	H1-hESC	embryonic stem cell:	n/a	n/a
42	CHD1	chr2:168148674-168148976	H1-hESC	embryonic stem cell:	n/a	n/a
43	CHD1	chr2:168149622-168149752	H1-hESC	embryonic stem cell:	n/a	n/a
44	CHD1	chr2:168148448-168150272	IMR90	lung:	n/a	chr2:168149149-168149159 chr2:168149142-168149152
45	CHD2	chr2:168149998-168150014	H1-hESC	embryonic stem cell:	n/a	n/a
46	CHD2	chr2:168188145-168188173	HepG2	liver:	n/a	n/a
47	CHD2	chr2:168151217-168151373	H1-hESC	embryonic stem cell:	n/a	n/a
48	CHD2	chr2:168149307-168149595	GM12878	blood:	n/a	n/a
49	CHD2	chr2:168149250-168149623	HepG2	liver:	n/a	n/a
50	CHD2	chr2:168188229-168188847	H1-hESC	embryonic stem cell:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:168150968-168151018	NT2-D1	testis:	n/a
2	chr2:168189841-168189891	BJ	skin:	n/a
3	chr2:168150968-168151018	NT2-D1	testis:	n/a
4	chr2:168189841-168189891	BJ	skin:	n/a
5	chr2:168150203-168150253	PFSK-1	brain:	n/a
6	chr2:168150968-168151018	NHDF-neo	bronchial:	n/a
7	chr2:168151051-168151101	ovcar-3	ovarian:	n/a
8	chr2:168188470-168188520	LNCaP	prostate:	n/a
9	chr2:168121101-168121151	NHBE	bronchial:	n/a
10	chr2:168189841-168189891	NHBE	bronchial:	n/a
11	chr2:168103543-168103593	HRCEpiC	kidney:	n/a
12	chr2:168139042-168139092	U87	brain:	n/a
13	chr2:168149519-168149569	HAEpiC	amniotic membrane:	n/a
14	chr2:168151004-168151054	SK-N-MC	brain:	n/a
15	chr2:168193427-168193477	NHDF-neo	bronchial:	n/a
16	chr2:168149519-168149569	PrEC	prostate:	n/a
17	chr2:168121101-168121151	PANC-1	pancreas:	n/a
18	chr2:168115266-168115316	Hepatocyte	liver:	n/a
19	chr2:168149991-168150041	ovcar-3	ovarian:	n/a
20	chr2:168139042-168139092	CMK	blood:	n/a
21	chr2:168148419-168148469	SK-N-SH	brain:	n/a
22	chr2:168104087-168104137	Hela-S3	cervix:	n/a
23	chr2:168150968-168151018	HUVEC	blood vessel:	n/a
24	chr2:168149991-168150041	PFSK-1	brain:	n/a
25	chr2:168193427-168193477	PFSK-1	brain:	n/a
26	chr2:168151004-168151054	MCF10A-Er-Src	breast:	n/a
27	chr2:168150968-168151018	PANC-1	pancreas:	n/a
28	chr2:168104087-168104137	RPTEC	kidney:	n/a
29	chr2:168103543-168103593	HMEC	breast:	n/a
30	chr2:168149519-168149569	AG04449	skin:	fetal
31	chr2:168188470-168188520	HPAEpiC	pulmonary alveolar:	n/a
32	chr2:168139042-168139092	HCF	heart:	n/a
33	chr2:168149991-168150041	HCT-116	colon:	n/a
34	chr2:168151051-168151101	GM12892	blood:	n/a
35	chr2:168145481-168145531	GM12878	blood:	n/a
36	chr2:168103475-168103525	AG04449	skin:	fetal
37	chr2:168139042-168139092	BJ	skin:	n/a
38	chr2:168149991-168150041	K562	blood:	n/a
39	chr2:168103475-168103525	HUVEC	blood vessel:	n/a
40	chr2:168189841-168189891	HCPEpiC	choroid plexus:	n/a
41	chr2:168115266-168115316	U87	brain:	n/a
42	chr2:168193427-168193477	Hela-S3	cervix:	n/a
43	chr2:168104087-168104137	HRCEpiC	kidney:	n/a
44	chr2:168151051-168151101	GM12891	blood:	n/a
45	chr2:168130989-168131039	SAEC	small airway:	n/a
46	chr2:168149519-168149569	Hepatocyte	liver:	n/a
47	chr2:168150203-168150253	AG09309	skin:	n/a
48	chr2:168139042-168139092	HRPEpiC	eye:	n/a
49	chr2:168149401-168149451	Jurkat	blood:	n/a
50	chr2:168103475-168103525	HIPEpiC	eye:	n/a

No.	Distal block	Cell Line	Cell type
1	chr2:168158037..168159768-chr2:168162619..168165474,2	K562	blood:
2	chr2:168144344..168146504-chr2:168147562..168149498,2	MCF-7	breast:
3	chr2:168143145..168144747-chr2:168145915..168147958,2	MCF-7	breast:
4	chr1:144532837..144535320-chr2:168191058..168192558,2	K562	blood:
5	chr13:71965413..71965933-chr2:168183503..168184104,2	MCF-7	breast:
6	chr2:168143145..168144747-chr2:168145915..168147958,2	MCF-7	breast:
7	chr2:168120817..168121511-chr2:168974628..168975875,3	MCF-7	breast:
8	chr2:168114351..168116891-chr2:168133743..168135416,2	K562	blood:
9	chr2:168120652..168121595-chr2:168406649..168407520,3	MCF-7	breast:
10	chr2:168158037..168159768-chr2:168162619..168165474,2	K562	blood:
11	chr1:144532923..144535291-chr2:168191058..168192578,2	K562	blood:
12	chr2:168132951..168134479-chr2:168142978..168144897,2	K562	blood:
13	chr2:168135885..168137977-chr2:168139008..168140759,2	MCF-7	breast:
14	chr2:167395562..167396116-chr2:168120687..168121387,2	MCF-7	breast:
15	chr2:168132951..168134479-chr2:168142978..168144897,2	K562	blood:
16	chr2:168112095..168114422-chr2:168116747..168119257,2	K562	blood:
17	chr2:168144344..168146504-chr2:168147562..168149498,2	MCF-7	breast:
18	chr2:168112095..168114422-chr2:168116747..168119257,2	K562	blood:
19	chr2:168145007..168147502-chr2:168153038..168154565,2	K562	blood:
20	chr2:168145007..168147502-chr2:168153038..168154565,2	K562	blood:
21	chr2:168114351..168116891-chr2:168133743..168135416,2	K562	blood:
22	chr2:168089396..168091403-chr2:168092947..168095096,2	K562	blood:
23	chr2:168089396..168091403-chr2:168092947..168095096,2	K562	blood:
24	chr2:168135885..168137977-chr2:168139008..168140759,2	MCF-7	breast:
25	chr2:168082475..168084083-chr2:168084397..168086061,2	MCF-7	breast:
26	chr2:168120621..168121190-chr2:168975724..168976236,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-XIRP2-1	chr2:168149681-168149844	XLOC_001742
2	lnc-STK39-6	chr2:168153621-168153899	NONHSAT075310
3	lnc-STK39-6	chr2:168153906-168153917	NONHSAT075310

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	XIRP2	hsa-miR-335-5p	chr2:168116170-168116194

Variant related genes	Relation type
ENSG00000228222	TF binding region
ENSG00000228222	CpG island
ENSG00000201699	chromatin interactions

Extended variants
information (count: 4373 )
Associated
traits (count: 49 )

Variant overlapped rSNPs/rCNVs (count:4373 , 50 per page) page: 1 2 3 4 5 6 7 ... 88

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7602119	chr2:168084857-168084858	ZNF genes & repeats Weak transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs573880997	chr2:168084955-168084956	ZNF genes & repeats Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs7575951	chr2:168085076-168085077	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs201254326	chr2:168085085-168085086	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs186919827	chr2:168085168-168085169	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs563265993	chr2:168085253-168085254	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs544287091	chr2:168085265-168085266	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs191392107	chr2:168085281-168085282	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs116355028	chr2:168085369-168085370	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs139817142	chr2:168085430-168085431	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs145292985	chr2:168085484-168085485	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs75829156	chr2:168085555-168085556	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs548672217	chr2:168085573-168085574	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs562480909	chr2:168085591-168085592	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs531242656	chr2:168085676-168085677	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs373622652	chr2:168085677-168085678	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs181463370	chr2:168085682-168085683	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs185908889	chr2:168085683-168085684	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs547109684	chr2:168085691-168085692	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs74740818	chr2:168085697-168085698	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs547630388	chr2:168085709-168085710	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs567421478	chr2:168085718-168085719	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs113516180	chr2:168085767-168085768	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs377595913	chr2:168085799-168085800	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs189760431	chr2:168085907-168085908	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs556219320	chr2:168085934-168085935	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs569229225	chr2:168085958-168085959	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs537897702	chr2:168085980-168085981	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs183132301	chr2:168085991-168085992	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs536059823	chr2:168086038-168086039	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs577727248	chr2:168086118-168086119	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs73029735	chr2:168086185-168086186	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs554364382	chr2:168086282-168086283	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs112747795	chr2:168086312-168086313	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs574177465	chr2:168086339-168086340	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs543287451	chr2:168086352-168086353	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs563078637	chr2:168086353-168086354	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs16853277	chr2:168086376-168086377	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs111426264	chr2:168086451-168086452	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs576418918	chr2:168086453-168086454	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs112201705	chr2:168086473-168086474	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs187650174	chr2:168086501-168086502	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs576866500	chr2:168086506-168086507	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs7580183	chr2:168086515-168086516	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs527405222	chr2:168086607-168086608	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs547205151	chr2:168086612-168086613	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs371383394	chr2:168086618-168086619	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs559942703	chr2:168086652-168086653	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs143641197	chr2:168086669-168086670	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs567440250	chr2:168086686-168086687	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:49)

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
Cancer	20164919	CNVD
Autism	22495311	CNVD
Autism	18522746	CNVD
Neurodevelopmental disorder	22521361	CNVD
Melanoma	18172304	CNVD
Cancer	16751803	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Seminomas	18059402	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
myoclonus epilepsy	18472482	CNVD
Benign familial neonatal-infantile seizures	18472482	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Lung cancer	18438408	CNVD
Mental retardation	22214275	CNVD
Glioblastoma	21080181	CNVD
small cell lung cancer	20016488	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Autism	18414403	CNVD
Developmental delay	21147756	CNVD
Prostate cancer	16573809	CNVD
Myelofibrosis	22110671	CNVD
Neonatal seizures	20384724	CNVD
severe myoclonic epilepsy of infancy	18294202	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Schizophrenia	21346763	CNVD

Chromatin state (count:1092 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:168056800-168114000	Weak transcription	Psoas Muscle	Psoas
2	chr2:168067400-168096000	Weak transcription	Left Ventricle	heart
3	chr2:168083800-168095800	Weak transcription	Skeletal Muscle Male	skeletal muscle
4	chr2:168084800-168085000	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
5	chr2:168084800-168085000	Genic enhancers	Skeletal Muscle Female	skeletal muscle
6	chr2:168085000-168085200	Strong transcription	Skeletal Muscle Female	skeletal muscle
7	chr2:168085000-168098600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
8	chr2:168085200-168097000	Weak transcription	Skeletal Muscle Female	skeletal muscle
9	chr2:168089400-168090000	Enhancers	Pancreatic Islets	Pancreatic Islet
10	chr2:168089800-168090200	Enhancers	iPS-15b Cell Line	embryonic stem cell
11	chr2:168095800-168112200	Strong transcription	Skeletal Muscle Male	skeletal muscle
12	chr2:168096000-168096200	Genic enhancers	Left Ventricle	heart
13	chr2:168096200-168096800	Strong transcription	Left Ventricle	heart
14	chr2:168096400-168098200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
15	chr2:168096800-168098800	Weak transcription	Left Ventricle	heart
16	chr2:168096800-168099000	Weak transcription	Right Ventricle	heart
17	chr2:168097000-168112200	Strong transcription	Skeletal Muscle Female	skeletal muscle
18	chr2:168097200-168099800	Weak transcription	Fetal Muscle Leg	muscle
19	chr2:168097400-168098000	Enhancers	Breast Myoepithelial Primary Cells	Breast
20	chr2:168097800-168109600	Weak transcription	Primary hematopoietic stem cells	blood
21	chr2:168098200-168100400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
22	chr2:168098600-168100400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
23	chr2:168098800-168100400	Strong transcription	Left Ventricle	heart
24	chr2:168099000-168100000	Strong transcription	Right Ventricle	heart
25	chr2:168099800-168100200	Strong transcription	Fetal Muscle Leg	muscle
26	chr2:168100000-168107200	Weak transcription	Right Ventricle	heart
27	chr2:168100200-168115600	Weak transcription	Fetal Muscle Leg	muscle
28	chr2:168100400-168103200	Weak transcription	Left Ventricle	heart
29	chr2:168100400-168103600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
30	chr2:168100400-168109400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
31	chr2:168103200-168104000	Strong transcription	Left Ventricle	heart
32	chr2:168104000-168122200	Weak transcription	Left Ventricle	heart
33	chr2:168109200-168110000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
34	chr2:168109200-168110000	Enhancers	Muscle Satellite Cultured Cells	--
35	chr2:168109200-168110000	Enhancers	Pancreatic Islets	Pancreatic Islet
36	chr2:168109400-168109600	Enhancers	HUES48 Cell Line	embryonic stem cell
37	chr2:168109400-168109600	Flanking Active TSS	NH-A	brain
38	chr2:168109400-168109800	Enhancers	iPS-18 Cell Line	embryonic stem cell
39	chr2:168109400-168110000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
40	chr2:168109400-168111200	Enhancers	Stomach Mucosa	stomach
41	chr2:168109600-168109800	Enhancers	Primary hematopoietic stem cells	blood
42	chr2:168109600-168110000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
43	chr2:168109600-168110000	Enhancers	NH-A	brain
44	chr2:168109800-168110000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
45	chr2:168109800-168110000	Enhancers	HUES6 Cell Line	embryonic stem cell
46	chr2:168109800-168111400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
47	chr2:168109800-168112000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
48	chr2:168110000-168110800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
49	chr2:168110000-168113200	Weak transcription	HUES6 Cell Line	embryonic stem cell
50	chr2:168110000-168113400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links