Variant report

Variant	nsv560347
Chromosome Location	chr12:117623651-117643067
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:562)
CpG islands
(count:1159)
Chromatin interactive
region (count:9)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:562 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr12:117630143-117630332	HepG2	liver:	n/a	n/a
2	ARID3A	chr12:117628068-117628388	HepG2	liver:	n/a	n/a
3	ATF2	chr12:117628317-117628658	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr12:117628211-117628505	H1-hESC	embryonic stem cell:	n/a	n/a
5	BCL3	chr12:117627961-117628653	A549	lung:	n/a	chr12:117628275-117628288
6	BCLAF1	chr12:117628016-117628465	GM12878	blood:	n/a	chr12:117628275-117628288
7	BHLHE40	chr12:117628030-117628472	GM12878	blood:	n/a	chr12:117628396-117628412
8	BHLHE40	chr12:117628020-117628510	HepG2	liver:	n/a	chr12:117628396-117628412
9	BHLHE40	chr12:117627458-117627779	K562	blood:	n/a	n/a
10	BHLHE40	chr12:117628039-117628578	K562	blood:	n/a	chr12:117628396-117628412
11	BRCA1	chr12:117627274-117627501	H1-hESC	embryonic stem cell:	n/a	n/a
12	BRCA1	chr12:117628223-117628451	Hela-S3	cervix:	n/a	n/a
13	CBX3	chr12:117631749-117632109	K562	blood:	n/a	n/a
14	CBX3	chr12:117639932-117640186	K562	blood:	n/a	n/a
15	CCNT2	chr12:117627544-117628483	K562	blood:	n/a	n/a
16	CEBPB	chr12:117626218-117626460	K562	blood:	n/a	chr12:117626300-117626311
17	CEBPB	chr12:117626221-117626425	K562	blood:	n/a	chr12:117626300-117626311
18	CEBPB	chr12:117626152-117626350	A549	lung:	n/a	chr12:117626300-117626311
19	CEBPB	chr12:117626133-117626459	IMR90	lung:	n/a	chr12:117626300-117626311
20	CEBPB	chr12:117626207-117626466	H1-hESC	embryonic stem cell:	n/a	chr12:117626300-117626311
21	CEBPB	chr12:117626186-117626448	HepG2	liver:	n/a	chr12:117626300-117626311
22	CEBPB	chr12:117629135-117629224	HepG2	liver:	n/a	chr12:117629166-117629177
23	CEBPB	chr12:117626229-117626351	HepG2	liver:	n/a	chr12:117626300-117626311
24	CEBPD	chr12:117628174-117628386	HepG2	liver:	n/a	n/a
25	CEBPD	chr12:117628136-117628495	HepG2	liver:	n/a	n/a
26	CHD1	chr12:117627356-117627699	H1-hESC	embryonic stem cell:	n/a	n/a
27	CHD1	chr12:117628014-117628223	H1-hESC	embryonic stem cell:	n/a	n/a
28	CHD2	chr12:117628027-117628237	K562	blood:	n/a	n/a
29	CHD2	chr12:117628045-117628427	H1-hESC	embryonic stem cell:	n/a	n/a
30	CHD2	chr12:117629767-117630160	H1-hESC	embryonic stem cell:	n/a	n/a
31	CHD2	chr12:117628034-117628487	Hela-S3	cervix:	n/a	n/a
32	CHD2	chr12:117628013-117628206	HepG2	liver:	n/a	n/a
33	CHD2	chr12:117627690-117627800	HepG2	liver:	n/a	n/a
34	CHD2	chr12:117627685-117627721	Hela-S3	cervix:	n/a	n/a
35	CREB1	chr12:117627539-117628532	GM12878	blood:	n/a	n/a
36	CREB1	chr12:117627976-117628492	H1-hESC	embryonic stem cell:	n/a	n/a
37	CREB1	chr12:117627413-117628637	HepG2	liver:	n/a	n/a
38	CREB1	chr12:117627970-117628529	A549	lung:	n/a	n/a
39	CTCF	chr12:117628160-117628310	GM12869	blood:	n/a	n/a
40	CTCF	chr12:117627411-117627460	Medullo	brain:	n/a	n/a
41	CTCF	chr12:117627374-117627379	GM12891	blood:	n/a	n/a
42	CTCF	chr12:117627393-117627505	MCF-7	breast:	n/a	n/a
43	CTCF	chr12:117627397-117627495	GM12878	blood:	n/a	n/a
44	CTCF	chr12:117628261-117628351	Kidney_OC	kidney:	n/a	n/a
45	CTCF	chr12:117627412-117627499	MCF-7	breast:	n/a	n/a
46	CTCF	chr12:117627378-117627524	Gliobla	brain:	n/a	n/a
47	CTCF	chr12:117627320-117627470	HMEC	breast:	n/a	n/a
48	CTCF	chr12:117627390-117627471	HepG2	liver:	n/a	n/a
49	CTCF	chr12:117627480-117627630	GM12865	blood:	n/a	n/a
50	CTCF	chr12:117627380-117627544	GM12891	blood:	n/a	n/a

(count:1159 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:117627651-117627701	NHBE	bronchial:	n/a
2	chr12:117627286-117627336	HCT-116	colon:	n/a
3	chr12:117628578-117628628	HPAEpiC	pulmonary alveolar:	n/a
4	chr12:117626777-117626827	BE2_C	brain:	n/a
5	chr12:117627223-117627273	NT2-D1	testis:	n/a
6	chr12:117628589-117628639	MCF-7	breast:	n/a
7	chr12:117628347-117628397	HAEpiC	amniotic membrane:	n/a
8	chr12:117627478-117627528	Jurkat	blood:	n/a
9	chr12:117627478-117627528	SAEC	small airway:	n/a
10	chr12:117627651-117627701	SK-N-SH_RA	brain:	n/a
11	chr12:117627897-117627947	T-47D	breast:	n/a
12	chr12:117627478-117627528	NHDF-neo	bronchial:	n/a
13	chr12:117628589-117628639	GM12892	blood:	n/a
14	chr12:117630719-117630769	AG09309	skin:	n/a
15	chr12:117628469-117628519	HRE	kidney:	n/a
16	chr12:117624653-117624703	GM12891	blood:	n/a
17	chr12:117627897-117627947	HEEpiC	esophagus:	n/a
18	chr12:117626777-117626827	U87	brain:	n/a
19	chr12:117628469-117628519	PANC-1	pancreas:	n/a
20	chr12:117627286-117627336	GM19239	blood:	n/a
21	chr12:117627651-117627701	GM06990	blood:	n/a
22	chr12:117627651-117627701	HMEC	breast:	n/a
23	chr12:117630719-117630769	Jurkat	blood:	n/a
24	chr12:117627651-117627701	HepG2	liver:	n/a
25	chr12:117628469-117628519	HRPEpiC	eye:	n/a
26	chr12:117630719-117630769	CMK	blood:	n/a
27	chr12:117627223-117627273	AoSMC	blood vessel:	n/a
28	chr12:117627478-117627528	HCT-116	colon:	n/a
29	chr12:117628487-117628537	GM19239	blood:	n/a
30	chr12:117627897-117627947	HUVEC	blood vessel:	n/a
31	chr12:117628469-117628519	IMR90	lung:	fetal
32	chr12:117627478-117627528	SK-N-MC	brain:	n/a
33	chr12:117628347-117628397	PrEC	prostate:	n/a
34	chr12:117627478-117627528	HepG2	liver:	n/a
35	chr12:117627464-117627514	HUVEC	blood vessel:	n/a
36	chr12:117628463-117628513	HMEC	breast:	n/a
37	chr12:117627450-117627500	IMR90	lung:	fetal
38	chr12:117627478-117627528	HCPEpiC	choroid plexus:	n/a
39	chr12:117628463-117628513	NT2-D1	testis:	n/a
40	chr12:117628589-117628639	HCM	heart:	n/a
41	chr12:117628463-117628513	AG09309	skin:	n/a
42	chr12:117628469-117628519	PrEC	prostate:	n/a
43	chr12:117627464-117627514	ECC-1	luminal epithelium:	n/a
44	chr12:117628463-117628513	HEK293	kidney:	embryo
45	chr12:117628589-117628639	GM06990	blood:	n/a
46	chr12:117626777-117626827	HNPCEpiC	eye:	n/a
47	chr12:117630719-117630769	RPTEC	kidney:	n/a
48	chr12:117628487-117628537	SK-N-SH	brain:	n/a
49	chr12:117628578-117628628	HCPEpiC	choroid plexus:	n/a
50	chr12:117626777-117626827	H1-hESC	embryonic stem cell:	embryo

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

No.	Distal block	Cell Line	Cell type
1	chr12:117638881..117640489-chr12:117642610..117644525,2	K562	blood:
2	chr12:117624519..117626038-chr12:117626822..117628477,2	MCF-7	breast:
3	chr12:117621580..117624392-chr12:117625961..117628023,2	K562	blood:
4	chr12:117592833..117593531-chr12:117627067..117627588,2	MCF-7	breast:
5	chr12:117619225..117621566-chr12:117623434..117626120,2	MCF-7	breast:
6	chr12:117638881..117640489-chr12:117642610..117644525,2	K562	blood:
7	chr12:117616960..117620689-chr12:117621446..117624982,5	K562	blood:
8	chr1:40723245..40724204-chr12:117627875..117628424,2	HCT-116	colon:
9	chr12:117627165..117629540-chr12:118540302..118543294,2	MCF-7	breast:

No data

Variant related genes	Relation type
FBXO21	TF binding region
FBXO21	CpG island
ENSG00000084073	chromatin interactions
ENSG00000176834	chromatin interactions
ENSG00000259943	chromatin interactions
ENSG00000135108	chromatin interactions

Extended variants
information (count: 841 )
Associated
traits (count: 69 )

Variant overlapped rSNPs/rCNVs (count:841 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7314778	chr12:117623651-117623652	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs184096039	chr12:117623660-117623661	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs574127210	chr12:117623684-117623685	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs144813697	chr12:117623692-117623693	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs141047469	chr12:117623714-117623715	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs188775508	chr12:117623747-117623748	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs544039310	chr12:117623770-117623771	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs577329286	chr12:117623812-117623813	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs386766741	chr12:117623824-117623825	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs12231821	chr12:117623825-117623826	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs141834206	chr12:117623840-117623841	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs369588989	chr12:117623860-117623861	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs559862595	chr12:117623872-117623873	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs180868601	chr12:117623873-117623874	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs370659967	chr12:117623899-117623900	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs147045149	chr12:117623925-117623926	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs563185255	chr12:117623961-117623962	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs138286010	chr12:117623972-117623973	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs552052041	chr12:117623974-117623975	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs143787632	chr12:117624059-117624060	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs534001565	chr12:117624094-117624095	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs184511048	chr12:117624099-117624100	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs538791391	chr12:117624102-117624103	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs555318384	chr12:117624123-117624124	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs190469773	chr12:117624159-117624160	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs143294914	chr12:117624175-117624176	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs555230863	chr12:117624180-117624181	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs182134207	chr12:117624189-117624190	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs12309102	chr12:117624234-117624235	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs376217557	chr12:117624245-117624246	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs185750462	chr12:117624249-117624250	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs201875226	chr12:117624255-117624256	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs577785552	chr12:117624294-117624295	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs576781247	chr12:117624311-117624312	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs373966599	chr12:117624387-117624388	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs4767516	chr12:117624418-117624419	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs190566350	chr12:117624424-117624425	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
38	rs113571728	chr12:117624429-117624430	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
39	rs372744220	chr12:117624432-117624433	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
40	rs542685942	chr12:117624435-117624436	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
41	rs563173061	chr12:117624527-117624528	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs141388879	chr12:117624537-117624538	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs372473729	chr12:117624539-117624540	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs375683106	chr12:117624540-117624541	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs11068394	chr12:117624557-117624558	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs377015086	chr12:117624620-117624621	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs7134622	chr12:117624631-117624632	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs113855995	chr12:117624669-117624670	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs181654270	chr12:117624685-117624686	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs527889313	chr12:117624746-117624747	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:69)

Disease	PMID	Source
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
Ewing''s sarcoma	21437220	CNVD
Testicular germ cell tumor	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Medulloblastoma	21979893	CNVD
Malaria	21533027	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Basal cell lymphoma	17053054	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Autism	22495311	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	21949216	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Acute myeloid leukemia	16864856	CNVD
Cancer	21637783	CNVD
Glioblastoma multiforme	21080181	CNVD
Renal cell carcinoma	19461508	CNVD
Burkitt''s lymphoma	18698080	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Glioblastoma multiforme	21390271	CNVD
Cancer	20164919	CNVD
Cancer	16751803	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Wilms tumour	21544195	CNVD
Ovarian cancer	21720365	CNVD
Colorectal cancer	16272173	CNVD
lymphocytic leukemia	21291569	CNVD
Breast cancer	17603634	CNVD
Breast cancer	16397240	CNVD
Sudden cardiac death	19188705	CNVD
Breast cancer	17133270	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Schizophrenia	18923514	CNVD
Schizophrenia	22241247	CNVD
Cryptorchidism	21048976	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Neuroblastoma	18923191	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Neuroblastoma	20406844	CNVD
Medulloblastoma	16783165	CNVD
mental retardation	16760730	CNVD
Breast cancer	21509527	CNVD
Breast cancer	21364760	CNVD
Lung adenocarcinoma	21045234	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	21806811	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD

Chromatin state (count:736 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:117580000-117625000	Strong transcription	Primary T cells fromperipheralblood	blood
2	chr12:117580000-117626800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
3	chr12:117580600-117625600	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
4	chr12:117581200-117624600	Strong transcription	Duodenum Mucosa	Duodenum
5	chr12:117581400-117624200	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
6	chr12:117581400-117625800	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
7	chr12:117582200-117625800	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
8	chr12:117582400-117624400	Strong transcription	Breast Myoepithelial Primary Cells	Breast
9	chr12:117585800-117625600	Strong transcription	Primary T helper cells PMA-I stimulated	--
10	chr12:117590000-117626200	Strong transcription	HUES48 Cell Line	embryonic stem cell
11	chr12:117590200-117626800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
12	chr12:117590600-117625400	Strong transcription	Sigmoid Colon	Sigmoid Colon
13	chr12:117590600-117625600	Strong transcription	iPS-20b Cell Line	embryonic stem cell
14	chr12:117590600-117625600	Strong transcription	Monocytes-CD14+_RO01746	blood
15	chr12:117590600-117625800	Strong transcription	HUES64 Cell Line	embryonic stem cell
16	chr12:117590800-117625200	Strong transcription	Brain Anterior Caudate	brain
17	chr12:117591000-117624600	Strong transcription	Primary T helper cells fromperipheralblood	blood
18	chr12:117593800-117625000	Strong transcription	H1 Cell Line	embryonic stem cell
19	chr12:117593800-117625600	Strong transcription	HUES6 Cell Line	embryonic stem cell
20	chr12:117593800-117625600	Strong transcription	Placenta	Placenta
21	chr12:117593800-117625800	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
22	chr12:117594000-117625800	Strong transcription	iPS-18 Cell Line	embryonic stem cell
23	chr12:117597600-117624400	Strong transcription	Fetal Intestine Large	intestine
24	chr12:117598600-117624600	Strong transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
25	chr12:117602200-117624600	Strong transcription	Primary B cells from cord blood	blood
26	chr12:117603400-117624600	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
27	chr12:117607800-117624600	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
28	chr12:117607800-117624600	Strong transcription	Brain Inferior Temporal Lobe	brain
29	chr12:117608400-117624600	Strong transcription	Brain Cingulate Gyrus	brain
30	chr12:117609800-117624800	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--
31	chr12:117610800-117624400	Strong transcription	Liver	Liver
32	chr12:117613400-117627400	Weak transcription	Small Intestine	intestine
33	chr12:117613600-117626400	Weak transcription	NHLF	lung
34	chr12:117613600-117626800	Weak transcription	Right Ventricle	heart
35	chr12:117614000-117626800	Weak transcription	Colonic Mucosa	Colon
36	chr12:117614200-117626600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
37	chr12:117615000-117626800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
38	chr12:117615400-117624000	Weak transcription	HSMMtube	muscle
39	chr12:117616400-117626000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
40	chr12:117616400-117626800	Weak transcription	Psoas Muscle	Psoas
41	chr12:117616400-117627000	Weak transcription	Right Atrium	heart
42	chr12:117616600-117626000	Strong transcription	NH-A	brain
43	chr12:117616800-117626000	Weak transcription	Lung	lung
44	chr12:117617200-117624400	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
45	chr12:117617600-117625400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
46	chr12:117618800-117624600	Strong transcription	Fetal Kidney	kidney
47	chr12:117619200-117623800	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
48	chr12:117619400-117624000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
49	chr12:117619400-117624600	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
50	chr12:117619400-117624800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--

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