Variant report

Variant	nsv834449
Chromosome Location	chr2:168340043-168511856
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	chr2:168407019-168407240	HepG2	liver:	n/a	n/a
2	ARID3A	chr2:168366053-168367307	HepG2	liver:	n/a	n/a
3	ATF1	chr2:168410922-168410993	K562	blood:	n/a	n/a
4	ATF2	chr2:168366134-168366559	H1-hESC	embryonic stem cell:	n/a	n/a
5	ATF2	chr2:168366027-168366508	H1-hESC	embryonic stem cell:	n/a	n/a
6	BATF	chr2:168401887-168402153	GM12878	blood:	n/a	n/a
7	BATF	chr2:168452681-168452904	GM12878	blood:	n/a	n/a
8	BATF	chr2:168452654-168452907	GM12878	blood:	n/a	n/a
9	BATF	chr2:168401891-168402098	GM12878	blood:	n/a	n/a
10	BHLHE40	chr2:168401260-168401415	K562	blood:	n/a	n/a
11	BHLHE40	chr2:168508086-168508467	HepG2	liver:	n/a	n/a
12	CCNT2	chr2:168431048-168431146	K562	blood:	n/a	n/a
13	CEBPB	chr2:168503865-168504125	A549	lung:	n/a	chr2:168503998-168504009 chr2:168503997-168504010 chr2:168503997-168504010
14	CEBPB	chr2:168436478-168436681	K562	blood:	n/a	chr2:168436537-168436548
15	CEBPB	chr2:168436375-168436672	H1-hESC	embryonic stem cell:	n/a	chr2:168436537-168436548
16	CEBPB	chr2:168497976-168498270	IMR90	lung:	n/a	chr2:168498090-168498101 chr2:168498090-168498099 chr2:168498088-168498099
17	CEBPB	chr2:168410242-168410566	HCT-116	colon:	n/a	chr2:168410359-168410372 chr2:168410359-168410372 chr2:168410359-168410370 chr2:168410359-168410370
18	CEBPB	chr2:168436387-168436704	A549	lung:	n/a	chr2:168436537-168436548
19	CEBPB	chr2:168412076-168412330	A549	lung:	n/a	chr2:168412165-168412178 chr2:168412167-168412178 chr2:168412224-168412237 chr2:168412225-168412236 chr2:168412167-168412178
20	CEBPB	chr2:168366936-168367258	HepG2	liver:	n/a	n/a
21	CEBPB	chr2:168503861-168504147	IMR90	lung:	n/a	chr2:168503998-168504009 chr2:168503997-168504010 chr2:168503997-168504010
22	CEBPB	chr2:168436372-168436724	HepG2	liver:	n/a	chr2:168436537-168436548
23	CEBPB	chr2:168497931-168498266	A549	lung:	n/a	chr2:168498090-168498101 chr2:168498090-168498099 chr2:168498088-168498099
24	CEBPB	chr2:168431974-168432260	HepG2	liver:	n/a	chr2:168432151-168432164 chr2:168432152-168432163
25	CEBPB	chr2:168503829-168504152	HepG2	liver:	n/a	chr2:168503998-168504009 chr2:168503997-168504010 chr2:168503997-168504010
26	CEBPB	chr2:168412081-168412369	HepG2	liver:	n/a	chr2:168412165-168412178 chr2:168412167-168412178 chr2:168412224-168412237 chr2:168412225-168412236 chr2:168412167-168412178
27	CEBPB	chr2:168460153-168460348	HepG2	liver:	n/a	n/a
28	CEBPB	chr2:168436390-168436698	IMR90	lung:	n/a	chr2:168436537-168436548
29	CEBPB	chr2:168436410-168436690	Hela-S3	cervix:	n/a	chr2:168436537-168436548
30	CEBPB	chr2:168384440-168384653	HepG2	liver:	n/a	chr2:168384548-168384559 chr2:168384546-168384563
31	CEBPB	chr2:168466857-168467122	A549	lung:	n/a	chr2:168466947-168466958 chr2:168466945-168466958
32	CEBPB	chr2:168460161-168460445	IMR90	lung:	n/a	n/a
33	CEBPB	chr2:168497944-168498269	HepG2	liver:	n/a	chr2:168498090-168498101 chr2:168498090-168498099 chr2:168498088-168498099
34	CEBPB	chr2:168503912-168504129	K562	blood:	n/a	chr2:168503998-168504009 chr2:168503997-168504010 chr2:168503997-168504010
35	CTCF	chr2:168451740-168451890	HepG2	liver:	n/a	n/a
36	CTCF	chr2:168362660-168362810	HBMEC	blood vessel:	n/a	chr2:168362726-168362735 chr2:168362725-168362738
37	CTCF	chr2:168447740-168447890	NHLF	lung:	n/a	n/a
38	CTCF	chr2:168407460-168407610	WERI-Rb-1	eye:	n/a	n/a
39	CTCF	chr2:168406893-168407400	MCF-7	breast:	n/a	chr2:168407129-168407147 chr2:168407124-168407145
40	CTCF	chr2:168406950-168407324	IMR90	lung:	n/a	chr2:168407129-168407147 chr2:168407124-168407145
41	CTCF	chr2:168407060-168407210	HCM	heart:	n/a	chr2:168407129-168407147 chr2:168407124-168407145
42	CTCF	chr2:168407046-168407263	LNCaP	prostate:	n/a	chr2:168407129-168407147 chr2:168407124-168407145
43	CTCF	chr2:168362600-168362750	HUVEC	blood vessel:	n/a	chr2:168362726-168362735 chr2:168362725-168362738
44	CTCF	chr2:168407422-168407508	GM19238	blood:	n/a	n/a
45	CTCF	chr2:168407100-168407250	MCF-7	breast:	n/a	chr2:168407129-168407147 chr2:168407124-168407145
46	CTCF	chr2:168407024-168407245	HUVEC	blood vessel:	n/a	chr2:168407129-168407147 chr2:168407124-168407145
47	CTCF	chr2:168407020-168407170	GM12866	blood:	n/a	chr2:168407129-168407147 chr2:168407124-168407145
48	CTCF	chr2:168402852-168402888	HUVEC	blood vessel:	n/a	n/a
49	CTCF	chr2:168407031-168407268	GM12878	blood:	n/a	chr2:168407129-168407147 chr2:168407124-168407145
50	CTCF	chr2:168407071-168407229	GM13977	blood:	n/a	chr2:168407129-168407147 chr2:168407124-168407145

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:168407472-168407522	AoSMC	blood vessel:	n/a
2	chr2:168407472-168407522	AoSMC	blood vessel:	n/a
3	chr2:168401402-168401452	Hepatocyte	liver:	n/a
4	chr2:168401402-168401452	PANC-1	pancreas:	n/a
5	chr2:168420831-168420881	NT2-D1	testis:	n/a
6	chr2:168407472-168407522	HRE	kidney:	n/a
7	chr2:168401353-168401403	AoSMC	blood vessel:	n/a
8	chr2:168401402-168401452	HRPEpiC	eye:	n/a
9	chr2:168420831-168420881	NB4	blood:	n/a
10	chr2:168401330-168401380	MCF10A-Er-Src	breast:	n/a
11	chr2:168401402-168401452	Caco-2	colon:	n/a
12	chr2:168401330-168401380	AG09319	gingival:	n/a
13	chr2:168401330-168401380	MCF-7	breast:	n/a
14	chr2:168401353-168401403	SK-N-SH	brain:	n/a
15	chr2:168401330-168401380	CMK	blood:	n/a
16	chr2:168463973-168464023	BE2_C	brain:	n/a
17	chr2:168441181-168441231	ECC-1	luminal epithelium:	n/a
18	chr2:168401402-168401452	GM12878	blood:	n/a
19	chr2:168420831-168420881	H1-hESC	embryonic stem cell:	embryo
20	chr2:168401402-168401452	NH-A	brain:	n/a
21	chr2:168401402-168401452	GM19239	blood:	n/a
22	chr2:168420831-168420881	HCT-116	colon:	n/a
23	chr2:168401330-168401380	HNPCEpiC	eye:	n/a
24	chr2:168401353-168401403	NH-A	brain:	n/a
25	chr2:168441181-168441231	AG09319	gingival:	n/a
26	chr2:168401353-168401403	AG04449	skin:	fetal
27	chr2:168401402-168401452	NHBE	bronchial:	n/a
28	chr2:168401402-168401452	HNPCEpiC	eye:	n/a
29	chr2:168401353-168401403	Caco-2	colon:	n/a
30	chr2:168463973-168464023	HPAEpiC	pulmonary alveolar:	n/a
31	chr2:168463973-168464023	Caco-2	colon:	n/a
32	chr2:168463973-168464023	HMEC	breast:	n/a
33	chr2:168441181-168441231	SK-N-SH_RA	brain:	n/a
34	chr2:168441181-168441231	IMR90	lung:	fetal
35	chr2:168407472-168407522	Hepatocyte	liver:	n/a
36	chr2:168401330-168401380	HL-60	blood:	n/a
37	chr2:168401402-168401452	IMR90	lung:	fetal
38	chr2:168401330-168401380	HAEpiC	amniotic membrane:	n/a
39	chr2:168420831-168420881	HCPEpiC	choroid plexus:	n/a
40	chr2:168401330-168401380	LNCaP	prostate:	n/a
41	chr2:168407472-168407522	H1-hESC	embryonic stem cell:	embryo
42	chr2:168441181-168441231	HL-60	blood:	n/a
43	chr2:168407472-168407522	GM19239	blood:	n/a
44	chr2:168401353-168401403	HepG2	liver:	n/a
45	chr2:168463973-168464023	NHBE	bronchial:	n/a
46	chr2:168441181-168441231	Jurkat	blood:	n/a
47	chr2:168441181-168441231	HAEpiC	amniotic membrane:	n/a
48	chr2:168401402-168401452	BE2_C	brain:	n/a
49	chr2:168401353-168401403	LNCaP	prostate:	n/a
50	chr2:168401353-168401403	Hela-S3	cervix:	n/a

No.	Distal block	Cell Line	Cell type
1	chr2:168412011..168414014-chr2:168467499..168469834,2	K562	blood:
2	chr2:167395944..167396563-chr2:168406690..168407659,4	MCF-7	breast:
3	chr2:168407166..168410060-chr2:168411860..168414676,3	K562	blood:
4	chr2:168432443..168434147-chr2:168458240..168461184,2	K562	blood:
5	chr2:168427437..168429430-chr2:168431335..168434015,2	K562	blood:
6	chr2:168436976..168439202-chr2:168443810..168446763,2	K562	blood:
7	chr2:168407166..168410060-chr2:168411860..168414676,3	K562	blood:
8	chr2:168342324..168343828-chr2:168369519..168372114,2	K562	blood:
9	chr2:168350817..168353056-chr2:168354971..168356552,2	K562	blood:
10	chr2:168408100..168409906-chr2:168410906..168413122,2	K562	blood:
11	chr2:168412011..168414014-chr2:168467499..168469834,2	K562	blood:
12	chr2:168427437..168429430-chr2:168431335..168434015,2	K562	blood:
13	chr2:168120652..168121595-chr2:168406649..168407520,3	MCF-7	breast:
14	chr2:168511059..168513910-chr2:168515507..168517847,2	K562	blood:
15	chr2:168385896..168387785-chr2:168389352..168392165,2	K562	blood:
16	chr2:168406722..168407375-chr2:168975138..168975697,2	MCF-7	breast:
17	chr2:168432443..168434147-chr2:168458240..168461184,2	K562	blood:
18	chr2:168436976..168439202-chr2:168443810..168446763,2	K562	blood:
19	chr2:168350817..168353056-chr2:168354971..168356552,2	K562	blood:
20	chr2:168342324..168343828-chr2:168369519..168372114,2	K562	blood:
21	chr2:168385896..168387785-chr2:168389352..168392165,2	K562	blood:
22	chr2:168408100..168409906-chr2:168410906..168413122,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-XIRP2-2	chr2:168393862-168393995	NONHSAT075311
2	lnc-XIRP2-2	chr2:168351651-168352135	NONHSAT075311
3	lnc-XIRP2-1	chr2:168414647-168414843	XLOC_001742
4	lnc-XIRP2-2	chr2:168394047-168394068	NONHSAT075311
5	lnc-STK39-5	chr2:168505171-168505388	expReg_chr2_12378_-
6	lnc-XIRP2-2	chr2:168393469-168395482	NONHSAT075312
7	lnc-XIRP2-2	chr2:168357672-168358076	NONHSAT075311
8	lnc-XIRP2-1	chr2:168346687-168346787	XLOC_001742

Variant related genes	Relation type
RNU7-148P	TF binding region
RNU7-148P	CpG island

Extended variants
information (count: 6471 )
Associated
traits (count: 52 )

Variant overlapped rSNPs/rCNVs (count:6471 , 50 per page) page: 1 2 3 4 5 6 7 ... 130

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs188548799	chr2:168340056-168340057	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs537847444	chr2:168340148-168340149	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs191645844	chr2:168340213-168340214	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs183088257	chr2:168340225-168340226	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs375787787	chr2:168340330-168340331	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs574818868	chr2:168340409-168340410	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs1919854	chr2:168340426-168340427	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
8	rs573779008	chr2:168340450-168340451	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs536007815	chr2:168340464-168340465	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs187018212	chr2:168340485-168340486	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs191260014	chr2:168340491-168340492	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs552261368	chr2:168340517-168340518	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs150209812	chr2:168340591-168340592	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs564180391	chr2:168340593-168340594	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs138738673	chr2:168340610-168340611	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs183757922	chr2:168340645-168340646	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs560604499	chr2:168340669-168340670	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs529478246	chr2:168340674-168340675	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs571943005	chr2:168340798-168340799	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs149344076	chr2:168340826-168340827	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs563177048	chr2:168340852-168340853	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs187709789	chr2:168340902-168340903	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs147125596	chr2:168340952-168340953	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs377239313	chr2:168340973-168340974	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs571185264	chr2:168340997-168340998	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs1983514	chr2:168341005-168341006	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
27	rs372725695	chr2:168341055-168341056	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs75763355	chr2:168341074-168341075	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs115441187	chr2:168341080-168341081	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs536042403	chr2:168341094-168341095	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs555987364	chr2:168341104-168341105	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs138534194	chr2:168341114-168341115	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs538583169	chr2:168341131-168341132	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs536753875	chr2:168341138-168341139	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs377158041	chr2:168341171-168341172	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs193283547	chr2:168341172-168341173	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs367569972	chr2:168341173-168341174	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs59702146	chr2:168341202-168341203	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs144054923	chr2:168341225-168341226	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs147299720	chr2:168341252-168341253	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs185651493	chr2:168341291-168341292	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs560391305	chr2:168341316-168341317	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs574133823	chr2:168341320-168341321	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs190117350	chr2:168341334-168341335	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs563113511	chr2:168341341-168341342	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs112713796	chr2:168341354-168341355	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs540721632	chr2:168341393-168341394	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs575111268	chr2:168341427-168341428	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs148763221	chr2:168341434-168341435	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs370152567	chr2:168341437-168341438	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:52)

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	17122850	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Breast cancer	22522925	CNVD
Prostate cancer	18632612	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:536 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:168337000-168340400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
2	chr2:168337000-168355400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
3	chr2:168337200-168348200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
4	chr2:168338200-168343600	Weak transcription	Cortex derived primary cultured neurospheres	brain
5	chr2:168338200-168348200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
6	chr2:168338200-168366000	Weak transcription	H1 Cell Line	embryonic stem cell
7	chr2:168338400-168340400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
8	chr2:168338400-168341000	Weak transcription	HUES64 Cell Line	embryonic stem cell
9	chr2:168338400-168349400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
10	chr2:168338400-168352400	Weak transcription	HUES6 Cell Line	embryonic stem cell
11	chr2:168338800-168340400	Weak transcription	HUES48 Cell Line	embryonic stem cell
12	chr2:168338800-168340600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
13	chr2:168340000-168342200	Enhancers	iPS-15b Cell Line	embryonic stem cell
14	chr2:168340200-168345600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
15	chr2:168340400-168341600	Enhancers	iPS-20b Cell Line	embryonic stem cell
16	chr2:168340400-168341600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
17	chr2:168340400-168342000	Enhancers	HUES48 Cell Line	embryonic stem cell
18	chr2:168340600-168341600	Enhancers	iPS-18 Cell Line	embryonic stem cell
19	chr2:168341000-168342200	Enhancers	HUES64 Cell Line	embryonic stem cell
20	chr2:168341600-168352600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
21	chr2:168341600-168352800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
22	chr2:168341600-168365200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
23	chr2:168342000-168345600	Weak transcription	HUES48 Cell Line	embryonic stem cell
24	chr2:168342200-168343800	Weak transcription	HUES64 Cell Line	embryonic stem cell
25	chr2:168342200-168352400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
26	chr2:168343600-168343800	Enhancers	Fetal Muscle Leg	muscle
27	chr2:168343600-168345200	Enhancers	Skeletal Muscle Female	skeletal muscle
28	chr2:168343600-168347600	Enhancers	Cortex derived primary cultured neurospheres	brain
29	chr2:168343600-168352400	Weak transcription	H9 Cell Line	embryonic stem cell
30	chr2:168343800-168344400	Enhancers	HUES64 Cell Line	embryonic stem cell
31	chr2:168344200-168344600	Enhancers	Brain Germinal Matrix	brain
32	chr2:168344200-168345000	Enhancers	Skeletal Muscle Male	skeletal muscle
33	chr2:168344400-168345600	Weak transcription	HUES64 Cell Line	embryonic stem cell
34	chr2:168344600-168345600	Weak transcription	Brain Germinal Matrix	brain
35	chr2:168344800-168345000	Enhancers	Brain Substantia Nigra	brain
36	chr2:168345000-168345800	Weak transcription	Skeletal Muscle Male	skeletal muscle
37	chr2:168345200-168345600	Weak transcription	Skeletal Muscle Female	skeletal muscle
38	chr2:168345600-168345800	Enhancers	Brain Germinal Matrix	brain
39	chr2:168345600-168346000	Enhancers	Skeletal Muscle Female	skeletal muscle
40	chr2:168345600-168346200	Enhancers	HUES48 Cell Line	embryonic stem cell
41	chr2:168345600-168346200	Enhancers	HUES64 Cell Line	embryonic stem cell
42	chr2:168345600-168346200	Enhancers	Fetal Lung	lung
43	chr2:168345600-168346800	Enhancers	Fetal Brain Male	brain
44	chr2:168345600-168347000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
45	chr2:168345600-168347200	Enhancers	Brain Inferior Temporal Lobe	brain
46	chr2:168345600-168347400	Enhancers	Breast Myoepithelial Primary Cells	Breast
47	chr2:168345800-168346000	Enhancers	Skeletal Muscle Male	skeletal muscle
48	chr2:168345800-168346400	Weak transcription	Brain Germinal Matrix	brain
49	chr2:168345800-168347200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
50	chr2:168345800-168347400	Enhancers	Colon Smooth Muscle	Colon

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