Variant report

Variant	nsv1049391
Chromosome Location	chr12:1589463-1622803
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:233)
CpG islands
(count:1160)
Chromatin interactive
region (count:20)
LncRNA
region (count:16)
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	ARID3A	chr12:1609241-1609640	K562	blood:	n/a	n/a
2	ATF1	chr12:1601112-1601913	K562	blood:	n/a	n/a
3	BACH1	chr12:1609449-1609649	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr12:1609474-1609653	K562	blood:	n/a	n/a
5	BHLHE40	chr12:1601355-1601799	K562	blood:	n/a	n/a
6	BHLHE40	chr12:1609129-1609807	K562	blood:	n/a	chr12:1609375-1609391
7	BHLHE40	chr12:1598063-1598396	GM12878	blood:	n/a	n/a
8	CBX3	chr12:1609251-1609834	K562	blood:	n/a	n/a
9	CCNT2	chr12:1601047-1601641	K562	blood:	n/a	n/a
10	CCNT2	chr12:1609272-1609981	K562	blood:	n/a	n/a
11	CEBPB	chr12:1598285-1598477	K562	blood:	n/a	n/a
12	CEBPB	chr12:1618373-1618530	A549	lung:	n/a	n/a
13	CEBPD	chr12:1601111-1601604	K562	blood:	n/a	n/a
14	CTCF	chr12:1612040-1612190	GM12864	blood:	n/a	n/a
15	CTCF	chr12:1612082-1612233	H1-hESC	embryonic stem cell:	n/a	n/a
16	CTCF	chr12:1605720-1605870	AG04449	skin:	n/a	n/a
17	CTCF	chr12:1612060-1612210	HRPEpiC	eye:	n/a	n/a
18	CTCF	chr12:1605660-1605810	NHDF-neo	bronchial:	n/a	n/a
19	CTCF	chr12:1612040-1612190	SAEC	small airway:	n/a	n/a
20	CTCF	chr12:1605800-1605950	BJ	skin:	n/a	n/a
21	CTCF	chr12:1612080-1612230	AG10803	skin:	n/a	n/a
22	CTCF	chr12:1612107-1612222	MCF-7	breast:	n/a	n/a
23	CTCF	chr12:1612100-1612250	WERI-Rb-1	eye:	n/a	n/a
24	CTCF	chr12:1612160-1612310	AG09319	gingival:	n/a	n/a
25	CTCF	chr12:1614879-1615117	H1-hESC	embryonic stem cell:	n/a	n/a
26	CTCF	chr12:1612120-1612270	HRPEpiC	eye:	n/a	n/a
27	CTCF	chr12:1614982-1615003	HepG2	liver:	n/a	n/a
28	CTCF	chr12:1613238-1613339	GM10248	blood:	n/a	n/a
29	CTCF	chr12:1614800-1615044	H1-hESC	embryonic stem cell:	n/a	n/a
30	CTCF	chr12:1612140-1612290	NHDF-neo	bronchial:	n/a	n/a
31	CTCF	chr12:1612100-1612250	BJ	skin:	n/a	n/a
32	CTCF	chr12:1611980-1612130	WERI-Rb-1	eye:	n/a	n/a
33	CTCF	chr12:1605752-1605849	NHEK	skin:	n/a	n/a
34	CTCF	chr12:1612120-1612270	AG10803	skin:	n/a	n/a
35	CTCF	chr12:1614900-1615050	HepG2	liver:	n/a	n/a
36	CTCF	chr12:1612380-1612530	SK-N-SH_RA	brain:	n/a	n/a
37	CTCF	chr12:1611840-1611990	HRPEpiC	eye:	n/a	n/a
38	CTCF	chr12:1612080-1612230	AG09319	gingival:	n/a	n/a
39	CTCF	chr12:1598220-1598370	AG04449	skin:	n/a	n/a
40	CTCF	chr12:1612080-1612230	A549	lung:	n/a	n/a
41	CTCF	chr12:1612060-1612210	GM12872	blood:	n/a	n/a
42	CTCF	chr12:1612060-1612210	AoAF	blood vessel:	n/a	n/a
43	CTCF	chr12:1605740-1605890	AG04449	skin:	n/a	n/a
44	CTCF	chr12:1609680-1609820	K562	blood:	n/a	n/a
45	CTCF	chr12:1612080-1612230	AG09309	skin:	n/a	n/a
46	CTCF	chr12:1605740-1605890	HMEC	breast:	n/a	n/a
47	CTCF	chr12:1614881-1615014	H1-hESC	embryonic stem cell:	n/a	n/a
48	CTCF	chr12:1597161-1597218	Pancreas_OC	pancreas:	n/a	n/a
49	CTCF	chr12:1612100-1612250	GM12872	blood:	n/a	n/a
50	CTCF	chr12:1612448-1612608	H1-hESC	embryonic stem cell:	n/a	n/a

(count:1160 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:1609463-1609513	SKMC	muscle:	n/a
2	chr12:1609463-1609513	SKMC	muscle:	n/a
3	chr12:1598243-1598293	GM06990	blood:	n/a
4	chr12:1609034-1609084	RPTEC	kidney:	n/a
5	chr12:1614380-1614430	HRE	kidney:	n/a
6	chr12:1605950-1606000	AoSMC	blood vessel:	n/a
7	chr12:1609463-1609513	GM06990	blood:	n/a
8	chr12:1609549-1609599	HCT-116	colon:	n/a
9	chr12:1608961-1609011	GM06990	blood:	n/a
10	chr12:1609470-1609520	NHDF-neo	bronchial:	n/a
11	chr12:1609741-1609791	NT2-D1	testis:	n/a
12	chr12:1608961-1609011	HRE	kidney:	n/a
13	chr12:1608961-1609011	HAEpiC	amniotic membrane:	n/a
14	chr12:1609369-1609419	RPTEC	kidney:	n/a
15	chr12:1614380-1614430	AoSMC	blood vessel:	n/a
16	chr12:1609741-1609791	NHDF-neo	bronchial:	n/a
17	chr12:1602312-1602362	SKMC	muscle:	n/a
18	chr12:1598243-1598293	RPTEC	kidney:	n/a
19	chr12:1598243-1598293	Hela-S3	cervix:	n/a
20	chr12:1609549-1609599	HL-60	blood:	n/a
21	chr12:1608961-1609011	MCF-7	breast:	n/a
22	chr12:1609369-1609419	GM12878	blood:	n/a
23	chr12:1609346-1609396	HCM	heart:	n/a
24	chr12:1598243-1598293	HEK293	kidney:	embryo
25	chr12:1612664-1612714	HAEpiC	amniotic membrane:	n/a
26	chr12:1609537-1609587	HL-60	blood:	n/a
27	chr12:1612664-1612714	SK-N-SH_RA	brain:	n/a
28	chr12:1609537-1609587	CMK	blood:	n/a
29	chr12:1609245-1609295	HPAEpiC	pulmonary alveolar:	n/a
30	chr12:1609741-1609791	MCF10A-Er-Src	breast:	n/a
31	chr12:1614439-1614489	HEK293	kidney:	embryo
32	chr12:1608961-1609011	NT2-D1	testis:	n/a
33	chr12:1609470-1609520	SK-N-MC	brain:	n/a
34	chr12:1609490-1609540	PANC-1	pancreas:	n/a
35	chr12:1609537-1609587	IMR90	lung:	fetal
36	chr12:1609034-1609084	AG09309	skin:	n/a
37	chr12:1609245-1609295	HEK293	kidney:	embryo
38	chr12:1614380-1614430	GM06990	blood:	n/a
39	chr12:1612770-1612820	SKMC	muscle:	n/a
40	chr12:1602312-1602362	PANC-1	pancreas:	n/a
41	chr12:1614439-1614489	Hela-S3	cervix:	n/a
42	chr12:1608961-1609011	HRCEpiC	kidney:	n/a
43	chr12:1614380-1614430	ovcar-3	ovarian:	n/a
44	chr12:1598243-1598293	SK-N-SH_RA	brain:	n/a
45	chr12:1612672-1612722	NB4	blood:	n/a
46	chr12:1609490-1609540	HUVEC	blood vessel:	n/a
47	chr12:1609245-1609295	NHBE	bronchial:	n/a
48	chr12:1609549-1609599	Caco-2	colon:	n/a
49	chr12:1609537-1609587	H1-hESC	embryonic stem cell:	embryo
50	chr12:1609034-1609084	CMK	blood:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr12:1585013..1587408-chr12:1589984..1592160,3	K562	blood:
2	chr12:1598160..1599823-chr12:1609239..1611026,2	K562	blood:
3	chr12:1603741..1607368-chr12:1607408..1611728,5	K562	blood:
4	chr12:1603741..1607368-chr12:1607408..1611728,5	K562	blood:
5	chr12:1598160..1599823-chr12:1609239..1611026,2	K562	blood:
6	chr12:1609960..1612455-chr12:1612690..1615017,2	K562	blood:
7	chr12:1590718..1593050-chr12:1598985..1600530,2	MCF-7	breast:
8	chr12:1607941..1609659-chr12:1618774..1621179,2	K562	blood:
9	chr12:1592609..1594282-chr12:1599555..1601526,2	K562	blood:
10	chr12:1607941..1609659-chr12:1618774..1621179,2	K562	blood:
11	chr12:1588629..1590747-chr12:1599822..1601479,2	K562	blood:
12	chr12:1588629..1590747-chr12:1599822..1601479,2	K562	blood:
13	chr12:1603741..1607368-chr12:1607408..1611542,6	K562	blood:
14	chr12:1609960..1612455-chr12:1612690..1615017,2	K562	blood:
15	chr12:1611483..1613501-chr12:1625253..1627123,2	K562	blood:
16	chr12:1592609..1594282-chr12:1599555..1601526,2	K562	blood:
17	chr12:1590718..1593050-chr12:1598985..1600530,2	MCF-7	breast:
18	chr12:1608089..1610158-chr12:1624609..1627312,2	K562	blood:
19	chr12:1571885..1573568-chr12:1607878..1609868,2	K562	blood:
20	chr12:1603741..1607368-chr12:1607408..1611542,6	K562	blood:

(count:16 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FBXL14-1	chr12:1611627-1612636	ENSG00000249628
2	lnc-ERC1-1	chr12:1611633-1612648	XLOC_009615
3	lnc-ERC1-1	chr12:1609691-1609942	XLOC_009615
4	lnc-ERC1-1	chr12:1611633-1613590	XLOC_009615
5	lnc-ERC1-1	chr12:1615325-1616484	ENSG00000249628
6	lnc-FBXL14-1	chr12:1609691-1609937	ENSG00000249628
7	lnc-ERC1-1	chr12:1615339-1616484	ENSG00000249628
8	lnc-ERC1-1	chr12:1611627-1612636	ENSG00000249628
9	lnc-ERC1-1	chr12:1609691-1609937	ENSG00000249628
10	lnc-FBXL14-1	chr12:1615325-1616484	ENSG00000249628
11	lnc-ERC1-1	chr12:1609657-1609942	XLOC_009615
12	lnc-ERC1-1	chr12:1615336-1616484	NONHSAT025400
13	lnc-ERC1-1	chr12:1615339-1616484	XLOC_009615
14	lnc-WNK1-3	chr12:1603215-1605096	NONHSAT025395
15	lnc-ERC1-1	chr12:1611633-1612648	ENSG00000249628
16	lnc-ERC1-1	chr12:1612440-1613590	NONHSAT025399

No data

Variant related genes	Relation type
LINC00942	TF binding region
LINC00942	CpG island
ATP8A2	miRNA target sites
PTPRK	miRNA target sites
PDCD10	miRNA target sites
RNMT	miRNA target sites
PRPF4B	miRNA target sites
ACP2	miRNA target sites

Extended variants
information (count: 1657 )
Associated
traits (count: 83 )

Variant overlapped rSNPs/rCNVs (count:1657 , 50 per page) page: 1 2 3 4 5 6 7 ... 34

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs16928481	chr12:1589463-1589464	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs557313978	chr12:1589529-1589530	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs572551994	chr12:1589566-1589567	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs192050523	chr12:1589711-1589712	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs553400283	chr12:1589733-1589734	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs184277574	chr12:1589787-1589788	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs7315267	chr12:1589821-1589822	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs563937150	chr12:1589828-1589829	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs575795285	chr12:1589865-1589866	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs201000621	chr12:1589867-1589868	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs111377772	chr12:1589868-1589869	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs202175301	chr12:1589869-1589870	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs34611964	chr12:1589870-1589871	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs200558930	chr12:1589871-1589872	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs7295516	chr12:1589904-1589905	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs7315390	chr12:1589914-1589915	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs113253674	chr12:1589932-1589933	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs569862848	chr12:1589955-1589956	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs11613546	chr12:1590013-1590014	Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs546830210	chr12:1590014-1590015	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs34724477	chr12:1590024-1590025	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs141237756	chr12:1590042-1590043	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs112807806	chr12:1590058-1590059	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs11609462	chr12:1590069-1590070	Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
25	rs568745420	chr12:1590077-1590078	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs188619330	chr12:1590080-1590081	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs534941348	chr12:1590110-1590111	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs73601936	chr12:1590148-1590149	Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs566092218	chr12:1590172-1590173	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs533569198	chr12:1590189-1590190	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs529899660	chr12:1590215-1590216	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs553605224	chr12:1590268-1590269	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs181074386	chr12:1590269-1590270	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs577894470	chr12:1590407-1590408	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs386759447	chr12:1590419-1590420	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs184362475	chr12:1590424-1590425	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs557265697	chr12:1590429-1590430	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs73601938	chr12:1590436-1590437	Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs546270391	chr12:1590442-1590443	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs73601940	chr12:1590444-1590445	Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs573236899	chr12:1590471-1590472	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs189290122	chr12:1590503-1590504	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs545249307	chr12:1590504-1590505	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs563354190	chr12:1590517-1590518	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs557087427	chr12:1590545-1590546	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs529159317	chr12:1590549-1590550	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs10848482	chr12:1590609-1590610	Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs182179007	chr12:1590627-1590628	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs7296411	chr12:1590628-1590629	Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs551028896	chr12:1590657-1590658	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:83)

Disease	PMID	Source
Myelofibrosis	22110671	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Glaucoma	21310917	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Malignant peripheral nerve sheath tumor	19844265	CNVD
Squamous cell cancer	19607727	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Hepatocellular carcinoma	16750200	CNVD
Breast cancer	17133270	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Mental retardation	17847001	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
abnormal development	18461090	CNVD
Ovarian cancer	20844748	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Medulloblastoma	16968546	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
Breast cancer	22032731	CNVD
Cancer	21183584	CNVD
Myxofibrosarcoma	16751306	CNVD
Non-small cell lung cancer	21829676	CNVD
Ovarian neoplasms	16753589	CNVD
Prostate cancer	21965145	CNVD
Acute myeloid leukemia	16864856	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Disorders of sex development	21048976	CNVD
Glioblastoma multiforme	21080181	CNVD
Liposarcoma	21253554	CNVD
Prostate cancer	19156837	CNVD
Emphysema	19352772	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Malignant germ cell tumour	17285132	CNVD
Melanoma	18172304	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Wilms tumour	21544195	CNVD
Squamous cell cancer	21044232	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	19960244	CNVD
Endometrial cancer	22040021	CNVD
Colorectal cancer	20709793	CNVD
Breast cancer	21264507	CNVD
Cancer	16751803	CNVD
Testicular cancer	18059402	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Seminomas	18059402	CNVD
Esophageal cancer	21851588	CNVD
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Testicular germ cell tumor	18059402	CNVD
Malaria	21533027	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Breast cancer	21364760	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Ewing''s sarcoma	17952124	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Breast cancer	21858162	CNVD
Breast cancer	21509527	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21785460	CNVD
Ovarian cancer	21720365	CNVD
Myelodysplastic syndrome	21251322	CNVD
Pleomorphic liposarcoma	18784837	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Schizophrenia	23813976	CNVD
Cancer	20164919	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Melanoma	20877625	CNVD

Chromatin state (count:888 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:1552800-1598000	Weak transcription	Esophagus	oesophagus
2	chr12:1558400-1599400	Weak transcription	Pancreas	Pancrea
3	chr12:1567400-1599600	Weak transcription	Gastric	stomach
4	chr12:1575200-1590000	Weak transcription	Liver	Liver
5	chr12:1579200-1598200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
6	chr12:1579600-1600200	Weak transcription	K562	blood
7	chr12:1583200-1597400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
8	chr12:1583200-1599000	Weak transcription	Primary B cells from peripheral blood	blood
9	chr12:1583400-1596000	Weak transcription	Primary T helper cells PMA-I stimulated	--
10	chr12:1583400-1596200	Weak transcription	Primary T cells from cord blood	blood
11	chr12:1583400-1599400	Weak transcription	HepG2	liver
12	chr12:1583400-1602800	Weak transcription	Primary neutrophils fromperipheralblood	blood
13	chr12:1583600-1591800	Weak transcription	Fetal Intestine Small	intestine
14	chr12:1583600-1596200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
15	chr12:1583600-1597200	Weak transcription	Thymus	Thymus
16	chr12:1583800-1596800	Weak transcription	Primary T helper cells fromperipheralblood	blood
17	chr12:1584000-1598000	Weak transcription	Aorta	Aorta
18	chr12:1584000-1599200	Weak transcription	Fetal Muscle Trunk	muscle
19	chr12:1584000-1599200	Weak transcription	Lung	lung
20	chr12:1584000-1599400	Weak transcription	Brain Cingulate Gyrus	brain
21	chr12:1584200-1597800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
22	chr12:1584200-1597800	Weak transcription	Brain Anterior Caudate	brain
23	chr12:1584200-1598000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
24	chr12:1584200-1598400	Weak transcription	Fetal Muscle Leg	muscle
25	chr12:1584200-1598800	Weak transcription	Left Ventricle	heart
26	chr12:1584200-1598800	Weak transcription	Rectal Smooth Muscle	rectum
27	chr12:1584200-1599000	Weak transcription	Brain Angular Gyrus	brain
28	chr12:1584200-1599400	Weak transcription	Right Ventricle	heart
29	chr12:1584400-1591000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
30	chr12:1584400-1598000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
31	chr12:1584400-1599000	Weak transcription	Primary hematopoietic stem cells	blood
32	chr12:1584400-1599600	Weak transcription	Ovary	ovary
33	chr12:1584600-1591200	Weak transcription	Fetal Stomach	stomach
34	chr12:1584600-1599200	Weak transcription	Brain Hippocampus Middle	brain
35	chr12:1584800-1590000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
36	chr12:1584800-1597600	Weak transcription	Sigmoid Colon	Sigmoid Colon
37	chr12:1584800-1598200	Weak transcription	Fetal Brain Female	brain
38	chr12:1584800-1599000	Weak transcription	Duodenum Smooth Muscle	Duodenum
39	chr12:1584800-1599200	Weak transcription	Colon Smooth Muscle	Colon
40	chr12:1584800-1599400	Weak transcription	HUES48 Cell Line	embryonic stem cell
41	chr12:1584800-1601400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
42	chr12:1584800-1604600	Weak transcription	Fetal Kidney	kidney
43	chr12:1585000-1590200	Weak transcription	Fetal Lung	lung
44	chr12:1585000-1590600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
45	chr12:1585000-1590600	Weak transcription	HSMMtube	muscle
46	chr12:1585000-1597400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
47	chr12:1585000-1597800	Weak transcription	NH-A	brain
48	chr12:1585000-1598600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
49	chr12:1585000-1599400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
50	chr12:1585000-1599400	Weak transcription	Fetal Brain Male	brain

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