Variant report

Variant	nsv1004431
Chromosome Location	chr2:148859099-149054114
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:938)
CpG islands
(count:183)
Chromatin interactive
region (count:43)
LncRNA
region (count:10)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:938 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:149002017-149002569	HepG2	liver:	n/a	chr2:149002050-149002066
2	ARID3A	chr2:149009605-149009760	HepG2	liver:	n/a	n/a
3	ARID3A	chr2:148959061-148959356	HepG2	liver:	n/a	n/a
4	ARID3A	chr2:148888294-148888308	HepG2	liver:	n/a	n/a
5	ARID3A	chr2:148920439-148920729	K562	blood:	n/a	n/a
6	ARID3A	chr2:148968850-148969044	HepG2	liver:	n/a	chr2:148969017-148969033
7	ATF1	chr2:149017285-149017419	K562	blood:	n/a	n/a
8	ATF1	chr2:148967322-148967474	K562	blood:	n/a	n/a
9	BACH1	chr2:149017369-149017502	H1-hESC	embryonic stem cell:	n/a	n/a
10	BACH1	chr2:148936476-148936481	H1-hESC	embryonic stem cell:	n/a	n/a
11	BACH1	chr2:149030956-149031246	H1-hESC	embryonic stem cell:	n/a	n/a
12	BACH1	chr2:149017398-149017543	K562	blood:	n/a	n/a
13	BATF	chr2:148880380-148880646	GM12878	blood:	n/a	chr2:148880539-148880550
14	BHLHE40	chr2:149011302-149011613	K562	blood:	n/a	n/a
15	BHLHE40	chr2:149017230-149017473	K562	blood:	n/a	n/a
16	BHLHE40	chr2:149002150-149002345	HepG2	liver:	n/a	n/a
17	CBX3	chr2:149011244-149011646	K562	blood:	n/a	n/a
18	CBX3	chr2:149011246-149011697	HCT-116	colon:	n/a	n/a
19	CBX3	chr2:148958977-148959378	K562	blood:	n/a	n/a
20	CBX3	chr2:149017230-149017609	K562	blood:	n/a	n/a
21	CEBPB	chr2:148993741-148993935	HepG2	liver:	n/a	n/a
22	CEBPB	chr2:149013459-149013924	MCF-7	breast:	n/a	chr2:149013700-149013711
23	CEBPB	chr2:149013595-149013834	H1-hESC	embryonic stem cell:	n/a	chr2:149013700-149013711
24	CEBPB	chr2:149036854-149037024	HepG2	liver:	n/a	chr2:149036949-149036960
25	CEBPB	chr2:149017197-149017491	A549	lung:	n/a	n/a
26	CEBPB	chr2:148890556-148890855	K562	blood:	n/a	chr2:148890713-148890724 chr2:148890713-148890726 chr2:148890713-148890726 chr2:148890713-148890726 chr2:148890714-148890725
27	CEBPB	chr2:148977144-148977344	HepG2	liver:	n/a	chr2:148977256-148977267
28	CEBPB	chr2:148890590-148890863	IMR90	lung:	n/a	chr2:148890713-148890724 chr2:148890713-148890726 chr2:148890713-148890726 chr2:148890713-148890726 chr2:148890714-148890725
29	CEBPB	chr2:149013365-149013868	Hela-S3	cervix:	n/a	chr2:149013700-149013711
30	CEBPB	chr2:149036906-149037097	H1-hESC	embryonic stem cell:	n/a	chr2:149036949-149036960
31	CEBPB	chr2:148958865-148959261	H1-hESC	embryonic stem cell:	n/a	n/a
32	CEBPB	chr2:149013272-149013893	IMR90	lung:	n/a	chr2:149013700-149013711
33	CEBPB	chr2:148896755-148896970	H1-hESC	embryonic stem cell:	n/a	chr2:148896831-148896842
34	CEBPB	chr2:149036772-149037160	MCF-7	breast:	n/a	chr2:149036949-149036960
35	CEBPB	chr2:148889960-148890414	A549	lung:	n/a	chr2:148890137-148890150 chr2:148890137-148890150
36	CEBPB	chr2:148890640-148890848	H1-hESC	embryonic stem cell:	n/a	chr2:148890713-148890724 chr2:148890713-148890726 chr2:148890713-148890726 chr2:148890713-148890726 chr2:148890714-148890725
37	CEBPB	chr2:149013483-149013811	A549	lung:	n/a	chr2:149013700-149013711
38	CEBPB	chr2:149017219-149017602	ECC-1	luminal epithelium:	n/a	n/a
39	CEBPB	chr2:149045883-149046183	IMR90	lung:	n/a	n/a
40	CEBPB	chr2:149036788-149037114	HepG2	liver:	n/a	chr2:149036949-149036960
41	CEBPB	chr2:148987418-148987618	HepG2	liver:	n/a	n/a
42	CEBPB	chr2:149036882-149037075	K562	blood:	n/a	chr2:149036949-149036960
43	CEBPB	chr2:148890651-148890853	A549	lung:	n/a	chr2:148890713-148890724 chr2:148890713-148890726 chr2:148890713-148890726 chr2:148890713-148890726 chr2:148890714-148890725
44	CEBPB	chr2:149013189-149013898	HepG2	liver:	n/a	chr2:149013700-149013711
45	CEBPB	chr2:149038716-149038999	IMR90	lung:	n/a	chr2:149038862-149038873
46	CEBPB	chr2:148915403-148915653	K562	blood:	n/a	n/a
47	CEBPB	chr2:148889991-148890325	Hela-S3	cervix:	n/a	chr2:148890137-148890150 chr2:148890137-148890150
48	CEBPB	chr2:149013233-149013884	A549	lung:	n/a	chr2:149013700-149013711
49	CEBPB	chr2:149036791-149037095	IMR90	lung:	n/a	chr2:149036949-149036960
50	CEBPB	chr2:149036773-149037143	HepG2	liver:	n/a	chr2:149036949-149036960

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:149041060-149041110	BJ	skin:	n/a
2	chr2:149041060-149041110	HCT-116	colon:	n/a
3	chr2:148893152-148893202	HIPEpiC	eye:	n/a
4	chr2:149041060-149041110	SK-N-MC	brain:	n/a
5	chr2:148893152-148893202	NH-A	brain:	n/a
6	chr2:148893152-148893202	A549	lung:	n/a
7	chr2:149041060-149041110	HEK293	kidney:	embryo
8	chr2:148976109-148976159	HIPEpiC	eye:	n/a
9	chr2:148976109-148976159	HUVEC	blood vessel:	n/a
10	chr2:148976109-148976159	HCF	heart:	n/a
11	chr2:148893152-148893202	SK-N-MC	brain:	n/a
12	chr2:148893152-148893202	HL-60	blood:	n/a
13	chr2:148893152-148893202	AG04450	lung:	fetal
14	chr2:148893152-148893202	AoSMC	blood vessel:	n/a
15	chr2:148976109-148976159	Hela-S3	cervix:	n/a
16	chr2:148976109-148976159	PrEC	prostate:	n/a
17	chr2:148893152-148893202	ECC-1	luminal epithelium:	n/a
18	chr2:149041060-149041110	SKMC	muscle:	n/a
19	chr2:148893152-148893202	HRCEpiC	kidney:	n/a
20	chr2:148976109-148976159	A549	lung:	n/a
21	chr2:149041060-149041110	HCM	heart:	n/a
22	chr2:148893152-148893202	HNPCEpiC	eye:	n/a
23	chr2:148976109-148976159	Caco-2	colon:	n/a
24	chr2:149041060-149041110	AG09319	gingival:	n/a
25	chr2:149041060-149041110	HUVEC	blood vessel:	n/a
26	chr2:149041060-149041110	GM06990	blood:	n/a
27	chr2:148893152-148893202	NT2-D1	testis:	n/a
28	chr2:149041060-149041110	HCF	heart:	n/a
29	chr2:148976109-148976159	HRPEpiC	eye:	n/a
30	chr2:148893152-148893202	GM12892	blood:	n/a
31	chr2:148976109-148976159	HEEpiC	esophagus:	n/a
32	chr2:149041060-149041110	MCF-7	breast:	n/a
33	chr2:149041060-149041110	GM12891	blood:	n/a
34	chr2:149041060-149041110	HepG2	liver:	n/a
35	chr2:148976109-148976159	SK-N-SH	brain:	n/a
36	chr2:148976109-148976159	BE2_C	brain:	n/a
37	chr2:149041060-149041110	SK-N-SH_RA	brain:	n/a
38	chr2:148893152-148893202	HepG2	liver:	n/a
39	chr2:149041060-149041110	RPTEC	kidney:	n/a
40	chr2:149041060-149041110	HEEpiC	esophagus:	n/a
41	chr2:149041060-149041110	Hela-S3	cervix:	n/a
42	chr2:148976109-148976159	GM12878	blood:	n/a
43	chr2:149041060-149041110	NHDF-neo	bronchial:	n/a
44	chr2:148893152-148893202	Jurkat	blood:	n/a
45	chr2:149041060-149041110	AG10803	skin:	n/a
46	chr2:148893152-148893202	AG09309	skin:	n/a
47	chr2:149041060-149041110	HRCEpiC	kidney:	n/a
48	chr2:148976109-148976159	NB4	blood:	n/a
49	chr2:149041060-149041110	T-47D	breast:	n/a
50	chr2:148976109-148976159	GM12891	blood:	n/a

(count:43 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:148884069..148886701-chr2:148890123..148892046,2	MCF-7	breast:
2	chr2:148931889..148933794-chr2:148936353..148939104,2	K562	blood:
3	chr2:148924504..148926944-chr2:148937289..148939887,2	MCF-7	breast:
4	chr2:148857706..148860074-chr2:148877712..148879777,2	K562	blood:
5	chr2:148960078..148961760-chr2:148963590..148966098,2	MCF-7	breast:
6	chr2:148994771..148998300-chr2:149002088..149006299,3	K562	blood:
7	chr2:148892318..148894319-chr2:148896559..148898244,2	MCF-7	breast:
8	chr2:148892318..148894319-chr2:148896559..148898244,2	MCF-7	breast:
9	chr2:148859675..148863197-chr2:148868107..148869963,3	MCF-7	breast:
10	chr2:148888593..148891096-chr2:148894086..148896797,2	K562	blood:
11	chr2:148869849..148872323-chr2:148885274..148887437,2	MCF-7	breast:
12	chr2:148994771..148998300-chr2:149002088..149006299,3	K562	blood:
13	chr2:148964117..148966027-chr2:148967186..148969154,2	MCF-7	breast:
14	chr2:148746466..148747928-chr2:148959011..148960040,7	MCF-7	breast:
15	chr2:148869849..148872323-chr2:148885274..148887437,2	MCF-7	breast:
16	chr2:148925257..148925927-chr2:149266799..149267551,3	MCF-7	breast:
17	chr2:148857706..148860074-chr2:148877712..148879777,2	K562	blood:
18	chr17:56708470..56709572-chr2:149008937..149009960,15	MCF-7	breast:
19	chr2:148967081..148967666-chr2:149266757..149267493,2	MCF-7	breast:
20	chr2:148960078..148961760-chr2:148963590..148966098,2	MCF-7	breast:
21	chr2:148888593..148891096-chr2:148894086..148896797,2	K562	blood:
22	chr17:56707733..56709409-chr2:149007940..149009460,7	MCF-7	breast:
23	chr17:56708724..56710145-chr2:149008940..149009960,20	MCF-7	breast:
24	chr2:148976677..148978352-chr2:149006227..149008013,2	MCF-7	breast:
25	chr2:148964117..148966027-chr2:148967186..148969154,2	MCF-7	breast:
26	chr2:148976677..148978352-chr2:149006227..149008013,2	MCF-7	breast:
27	chr2:148695045..148696010-chr2:148958677..148959570,5	K562	blood:
28	chr2:148924504..148926944-chr2:148937289..148939887,2	MCF-7	breast:
29	chr2:148951330..148953430-chr2:148956133..148959129,2	K562	blood:
30	chr2:148852527..148854088-chr2:148860647..148862456,2	MCF-7	breast:
31	chr2:148996066..148998300-chr2:149002088..149004966,2	K562	blood:
32	chr2:148862754..148865628-chr2:148893706..148895344,2	K562	blood:
33	chr2:148862754..148865628-chr2:148893706..148895344,2	K562	blood:
34	chr2:148777816..148780257-chr2:148961269..148962957,2	MCF-7	breast:
35	chr17:56707881..56710421-chr2:149007960..149010940,2	K562	blood:
36	chr2:148859675..148863197-chr2:148868107..148869963,3	MCF-7	breast:
37	chr17:56707748..56709669-chr2:149007960..149010940,5	MCF-7	breast:
38	chr2:148884069..148886701-chr2:148890123..148892046,2	MCF-7	breast:
39	chr2:148995742..148998637-chr2:149000873..149004003,3	MCF-7	breast:
40	chr2:148995742..148998637-chr2:149000873..149004003,3	MCF-7	breast:
41	chr2:148931889..148933794-chr2:148936353..148939104,2	K562	blood:
42	chr2:148996066..148998300-chr2:149002088..149004966,2	K562	blood:
43	chr2:148951330..148953430-chr2:148956133..148959129,2	K562	blood:

(count:10 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-MBD5-1	chr2:148936269-148936362	NONHSAT074875
2	lnc-MBD5-1	chr2:148936269-148936362	NONHSAT074878
3	lnc-ORC4-3	chr2:149053225-149054248	NONHSAT074880
4	lnc-MBD5-1	chr2:148977516-148977602	NONHSAT074878
5	lnc-MBD5-1	chr2:148990814-148990964	NONHSAT074872
6	lnc-MBD5-1	chr2:148936269-148936362	NONHSAT074874
7	lnc-MBD5-1	chr2:148990814-148990896	NONHSAT074874
8	lnc-MBD5-1	chr2:148936269-148936362	NONHSAT074871
9	lnc-MBD5-1	chr2:148936269-148936362	NONHSAT074872
10	lnc-MBD5-1	chr2:148990814-148990964	NONHSAT074878

No data

Variant related genes	Relation type
ENSG00000212181	TF binding region
ENSG00000212181	CpG island
ENSG00000115947	chromatin interactions
ENSG00000212195	chromatin interactions
ENSG00000204406	chromatin interactions

Extended variants
information (count: 6706 )
Associated
traits (count: 56 )

Variant overlapped rSNPs/rCNVs (count:6706 , 50 per page) page: 1 2 3 4 5 6 7 ... 135

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs73007179	chr2:148859145-148859146	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs545377374	chr2:148859194-148859195	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs564052967	chr2:148859221-148859222	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs1227484	chr2:148859296-148859297	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs549329480	chr2:148859349-148859350	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs568725052	chr2:148859354-148859355	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs567336960	chr2:148859355-148859356	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs537623744	chr2:148859420-148859421	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs528546667	chr2:148859427-148859428	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs546717293	chr2:148859500-148859501	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs73007180	chr2:148859640-148859641	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs182752672	chr2:148859721-148859722	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs113418197	chr2:148859857-148859858	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs556885992	chr2:148859858-148859859	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs200625046	chr2:148859871-148859872	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs569088655	chr2:148859938-148859939	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs77236600	chr2:148859966-148859967	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs546025333	chr2:148859984-148859985	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs187732201	chr2:148859987-148859988	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs572909868	chr2:148860015-148860016	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs73007183	chr2:148860029-148860030	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs143752488	chr2:148860051-148860052	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs189741719	chr2:148860065-148860066	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs528534134	chr2:148860070-148860071	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs183063320	chr2:148860124-148860125	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs563749626	chr2:148860135-148860136	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs543307065	chr2:148860166-148860167	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs542983778	chr2:148860190-148860191	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs1237097	chr2:148860200-148860201	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs560921307	chr2:148860204-148860205	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs187830393	chr2:148860206-148860207	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs113654978	chr2:148860233-148860234	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs71835352	chr2:148860234-148860235	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs546678669	chr2:148860253-148860254	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs33982033	chr2:148860254-148860255	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs72868772	chr2:148860255-148860256	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs532501395	chr2:148860257-148860258	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs72105542	chr2:148860270-148860271	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs559174208	chr2:148860291-148860292	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs11687411	chr2:148860298-148860299	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs368741045	chr2:148860299-148860300	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs2442764	chr2:148860300-148860301	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs70992193	chr2:148860301-148860302	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs58945611	chr2:148860302-148860303	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs200339163	chr2:148860308-148860309	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs201472297	chr2:148860310-148860311	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs540940902	chr2:148860323-148860324	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs371487044	chr2:148860331-148860332	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs139755486	chr2:148860332-148860333	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs201431367	chr2:148860335-148860336	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:56)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Breast cancer	17603634	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	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
epilepsy	18472482	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
lymphocytic leukemia	21291569	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	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
Prostate cancer	18632612	CNVD
Lung cancer	18438408	CNVD
Mental retardation	22214275	CNVD
Glioblastoma	21080181	CNVD
small cell lung cancer	20016488	CNVD
Epilepsy	19904302	CNVD
Intellectual disability	19904302	CNVD
Microcephaly	19904302	CNVD
severe speech impairment	19904302	CNVD
Mental retardation	20152051	CNVD
2q23.1 microdeletion syndrome	18812405	CNVD
Mental retardation	19809484	CNVD
Autism	21981781	CNVD
Breast cancer	22522925	CNVD
Mental retardation	17847001	CNVD
Hodgkin''s lymphoma	18179710	CNVD
Autism	20531469	CNVD

Chromatin state (count:1604 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:148826000-148861000	Weak transcription	Left Ventricle	heart
2	chr2:148837600-148866800	Weak transcription	Ovary	ovary
3	chr2:148843600-148860600	Weak transcription	Brain Hippocampus Middle	brain
4	chr2:148845400-148866000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr2:148845400-148868000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
6	chr2:148851800-148867600	Weak transcription	Primary T cells from cord blood	blood
7	chr2:148854800-148874000	Weak transcription	Primary B cells from cord blood	blood
8	chr2:148855800-148901000	Weak transcription	Fetal Intestine Small	intestine
9	chr2:148857000-148861000	Weak transcription	Brain Angular Gyrus	brain
10	chr2:148857800-148859800	Weak transcription	Pancreatic Islets	Pancreatic Islet
11	chr2:148858400-148861000	Weak transcription	Aorta	Aorta
12	chr2:148859400-148859600	Enhancers	Fetal Brain Male	brain
13	chr2:148859400-148859600	Enhancers	Rectal Smooth Muscle	rectum
14	chr2:148859600-148860200	Weak transcription	Rectal Smooth Muscle	rectum
15	chr2:148859600-148860400	Enhancers	Colon Smooth Muscle	Colon
16	chr2:148859600-148867000	Weak transcription	Fetal Brain Male	brain
17	chr2:148859800-148860000	Enhancers	Pancreatic Islets	Pancreatic Islet
18	chr2:148859800-148860200	Enhancers	Stomach Smooth Muscle	stomach
19	chr2:148859800-148861200	Enhancers	Brain Cingulate Gyrus	brain
20	chr2:148860000-148861200	Enhancers	Brain Inferior Temporal Lobe	brain
21	chr2:148860000-148861600	Weak transcription	Pancreatic Islets	Pancreatic Islet
22	chr2:148860200-148860400	Enhancers	Rectal Smooth Muscle	rectum
23	chr2:148860200-148860400	Enhancers	Right Atrium	heart
24	chr2:148860400-148861600	Weak transcription	Colon Smooth Muscle	Colon
25	chr2:148860400-148861600	Weak transcription	Rectal Smooth Muscle	rectum
26	chr2:148860600-148861000	Enhancers	Brain Hippocampus Middle	brain
27	chr2:148860600-148861200	Enhancers	Primary neutrophils fromperipheralblood	blood
28	chr2:148860600-148861200	Enhancers	Brain Substantia Nigra	brain
29	chr2:148861000-148861200	Enhancers	Aorta	Aorta
30	chr2:148861000-148861200	Enhancers	Brain Angular Gyrus	brain
31	chr2:148861000-148861200	Enhancers	Left Ventricle	heart
32	chr2:148861000-148861200	Enhancers	Right Atrium	heart
33	chr2:148861000-148862000	Enhancers	ES-I3 Cell Line	embryonic stem cell
34	chr2:148861200-148889000	Weak transcription	Aorta	Aorta
35	chr2:148861400-148862400	Enhancers	HUES48 Cell Line	embryonic stem cell
36	chr2:148861600-148861800	Enhancers	Rectal Smooth Muscle	rectum
37	chr2:148861600-148862000	Enhancers	HUES6 Cell Line	embryonic stem cell
38	chr2:148861600-148862000	Enhancers	HUES64 Cell Line	embryonic stem cell
39	chr2:148861600-148862000	Enhancers	iPS-15b Cell Line	embryonic stem cell
40	chr2:148861600-148862000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
41	chr2:148861600-148862000	Enhancers	Colon Smooth Muscle	Colon
42	chr2:148861600-148862000	Enhancers	Pancreatic Islets	Pancreatic Islet
43	chr2:148861800-148862400	Enhancers	iPS-18 Cell Line	embryonic stem cell
44	chr2:148861800-148862400	Enhancers	iPS-20b Cell Line	embryonic stem cell
45	chr2:148862000-148869800	Weak transcription	Pancreatic Islets	Pancreatic Islet
46	chr2:148862800-148863000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
47	chr2:148863000-148881600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
48	chr2:148863800-148864800	Enhancers	Osteobl	bone
49	chr2:148864000-148865200	Enhancers	Muscle Satellite Cultured Cells	--
50	chr2:148864000-148881200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood

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