Variant report

Variant	nsv560495
Chromosome Location	chr12:124012974-124017461
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:144)
CpG islands
(count:122)
Chromatin interactive
region (count:24)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:144 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr12:124017367-124017624	K562	blood:	n/a	n/a
2	BCL11A	chr12:124016656-124016943	GM12878	blood:	n/a	chr12:124016835-124016844
3	BCL3	chr12:124015207-124015490	GM12878	blood:	n/a	n/a
4	BCLAF1	chr12:124016596-124017027	GM12878	blood:	n/a	chr12:124016835-124016844
5	BHLHE40	chr12:124017420-124018105	K562	blood:	n/a	chr12:124017636-124017652
6	BHLHE40	chr12:124016448-124016532	K562	blood:	n/a	n/a
7	BRCA1	chr12:124017418-124017970	Hela-S3	cervix:	n/a	n/a
8	CBX3	chr12:124017259-124018108	K562	blood:	n/a	n/a
9	CEBPB	chr12:124017334-124018091	Hela-S3	cervix:	n/a	n/a
10	CHD2	chr12:124017413-124018001	K562	blood:	n/a	n/a
11	CHD2	chr12:124016787-124016860	K562	blood:	n/a	n/a
12	CUX1	chr12:124017425-124017512	K562	blood:	n/a	n/a
13	E2F6	chr12:124017363-124018308	H1-hESC	embryonic stem cell:	n/a	n/a
14	E2F6	chr12:124017443-124018183	A549	lung:	n/a	n/a
15	EBF1	chr12:124016789-124016903	GM12878	blood:	n/a	n/a
16	EBF1	chr12:124016665-124016903	GM12878	blood:	n/a	n/a
17	ELF1	chr12:124017324-124017932	A549	lung:	n/a	chr12:124017651-124017664
18	ELF1	chr12:124017385-124018213	MCF-7	breast:	n/a	chr12:124017651-124017664
19	ELF1	chr12:124017440-124017865	K562	blood:	n/a	chr12:124017651-124017664
20	ELF1	chr12:124017362-124017936	K562	blood:	n/a	chr12:124017651-124017664
21	ELF1	chr12:124017437-124017831	HepG2	liver:	n/a	chr12:124017651-124017664
22	ELF1	chr12:124017322-124017956	A549	lung:	n/a	chr12:124017651-124017664
23	ELF1	chr12:124017443-124017964	GM12878	blood:	n/a	chr12:124017651-124017664
24	EP300	chr12:124017388-124017540	K562	blood:	n/a	n/a
25	EP300	chr12:124016661-124016963	GM12878	blood:	n/a	chr12:124016839-124016848 chr12:124016835-124016849
26	IRF4	chr12:124016529-124017044	GM12878	blood:	n/a	n/a
27	MAFK	chr12:124017321-124017328	K562	blood:	n/a	n/a
28	MAX	chr12:124017269-124019274	A549	lung:	n/a	chr12:124019137-124019147 chr12:124017624-124017639
29	MAX	chr12:124017255-124019286	HepG2	liver:	n/a	chr12:124019137-124019147 chr12:124017624-124017639
30	MAX	chr12:124017421-124018127	K562	blood:	n/a	chr12:124017624-124017639
31	MAX	chr12:124017425-124018291	H1-hESC	embryonic stem cell:	n/a	chr12:124017624-124017639
32	MAX	chr12:124017326-124019119	K562	blood:	n/a	chr12:124017624-124017639
33	MAX	chr12:124017277-124018148	HCT-116	colon:	n/a	chr12:124017624-124017639
34	MAX	chr12:124017309-124019259	HepG2	liver:	n/a	chr12:124019137-124019147 chr12:124017624-124017639
35	MAX	chr12:124017408-124018178	SK-N-SH	brain:	n/a	chr12:124017624-124017639
36	MAX	chr12:124014390-124014608	K562	blood:	n/a	chr12:124014525-124014535
37	MAX	chr12:124017446-124019193	K562	blood:	n/a	chr12:124019137-124019147 chr12:124017624-124017639
38	MAX	chr12:124017303-124018190	H1-hESC	embryonic stem cell:	n/a	chr12:124017624-124017639
39	MAX	chr12:124017459-124018605	Hela-S3	cervix:	n/a	chr12:124017624-124017639
40	MAX	chr12:124016594-124017026	K562	blood:	n/a	chr12:124016824-124016835
41	MAX	chr12:124017437-124018147	SK-N-SH	brain:	n/a	chr12:124017624-124017639
42	MAX	chr12:124017255-124019402	A549	lung:	n/a	chr12:124019137-124019147 chr12:124017624-124017639
43	MAX	chr12:124017452-124018226	ECC-1	luminal epithelium:	n/a	chr12:124017624-124017639
44	MAX	chr12:124014461-124014648	NB4	blood:	n/a	chr12:124014525-124014535
45	MAX	chr12:124017423-124018547	MCF-7	breast:	n/a	chr12:124017624-124017639
46	MAX	chr12:124016614-124016974	NB4	blood:	n/a	chr12:124016824-124016835
47	MAZ	chr12:124016579-124019401	IMR90	lung:	n/a	chr12:124019137-124019147 chr12:124016824-124016835 chr12:124017249-124017259 chr12:124017624-124017639
48	MAZ	chr12:124017011-124017093	K562	blood:	n/a	n/a
49	MAZ	chr12:124017387-124018114	HepG2	liver:	n/a	chr12:124017624-124017639
50	MTA3	chr12:124016504-124017129	GM12878	blood:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:124016861-124016911	LNCaP	prostate:	n/a
2	chr12:124016861-124016911	RPTEC	kidney:	n/a
3	chr12:124014409-124014459	HL-60	blood:	n/a
4	chr12:124014409-124014459	HepG2	liver:	n/a
5	chr12:124016861-124016911	HCPEpiC	choroid plexus:	n/a
6	chr12:124016861-124016911	Jurkat	blood:	n/a
7	chr12:124016861-124016911	A549	lung:	n/a
8	chr12:124014409-124014459	GM12892	blood:	n/a
9	chr12:124016861-124016911	AG10803	skin:	n/a
10	chr12:124014409-124014459	HEK293	kidney:	embryo
11	chr12:124014409-124014459	K562	blood:	n/a
12	chr12:124014409-124014459	GM19239	blood:	n/a
13	chr12:124014409-124014459	CMK	blood:	n/a
14	chr12:124016861-124016911	IMR90	lung:	fetal
15	chr12:124016861-124016911	HepG2	liver:	n/a
16	chr12:124016861-124016911	AG04449	skin:	fetal
17	chr12:124014409-124014459	LNCaP	prostate:	n/a
18	chr12:124016861-124016911	PrEC	prostate:	n/a
19	chr12:124016861-124016911	Caco-2	colon:	n/a
20	chr12:124016861-124016911	BJ	skin:	n/a
21	chr12:124014409-124014459	HRE	kidney:	n/a
22	chr12:124014409-124014459	HPAEpiC	pulmonary alveolar:	n/a
23	chr12:124016861-124016911	HNPCEpiC	eye:	n/a
24	chr12:124014409-124014459	Caco-2	colon:	n/a
25	chr12:124016861-124016911	HEK293	kidney:	embryo
26	chr12:124016861-124016911	HCM	heart:	n/a
27	chr12:124014409-124014459	HIPEpiC	eye:	n/a
28	chr12:124014409-124014459	ProgFib	skin:	n/a
29	chr12:124016861-124016911	GM06990	blood:	n/a
30	chr12:124014409-124014459	U87	brain:	n/a
31	chr12:124014409-124014459	BJ	skin:	n/a
32	chr12:124016861-124016911	NHBE	bronchial:	n/a
33	chr12:124014409-124014459	AG09309	skin:	n/a
34	chr12:124016861-124016911	HMEC	breast:	n/a
35	chr12:124014409-124014459	SAEC	small airway:	n/a
36	chr12:124016861-124016911	HRCEpiC	kidney:	n/a
37	chr12:124016861-124016911	K562	blood:	n/a
38	chr12:124014409-124014459	HRPEpiC	eye:	n/a
39	chr12:124014409-124014459	NH-A	brain:	n/a
40	chr12:124014409-124014459	Hela-S3	cervix:	n/a
41	chr12:124014409-124014459	BE2_C	brain:	n/a
42	chr12:124016861-124016911	HCT-116	colon:	n/a
43	chr12:124014409-124014459	IMR90	lung:	fetal
44	chr12:124014409-124014459	NHBE	bronchial:	n/a
45	chr12:124014409-124014459	MCF10A-Er-Src	breast:	n/a
46	chr12:124016861-124016911	SAEC	small airway:	n/a
47	chr12:124014409-124014459	GM12891	blood:	n/a
48	chr12:124016861-124016911	T-47D	breast:	n/a
49	chr12:124014409-124014459	AoSMC	blood vessel:	n/a
50	chr12:124016861-124016911	HIPEpiC	eye:	n/a

(count:24 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:124014995..124016623-chr12:124054786..124056310,2	MCF-7	breast:
2	chr12:123988823..123991080-chr12:124013221..124015111,2	K562	blood:
3	chr12:123943032..123944561-chr12:124016969..124018583,2	MCF-7	breast:
4	chr12:124008800..124013373-chr12:124015066..124019267,4	K562	blood:
5	chr12:123955912..123957787-chr12:124014886..124016796,2	K562	blood:
6	chr12:123942564..123944577-chr12:124016063..124019666,4	MCF-7	breast:
7	chr12:123948940..123951509-chr12:124017235..124019368,2	MCF-7	breast:
8	chr12:123872416..123876102-chr12:124017252..124019601,4	MCF-7	breast:
9	chr12:123947470..123950375-chr12:124015636..124018854,3	K562	blood:
10	chr12:124013201..124014769-chr12:124068693..124071334,2	MCF-7	breast:
11	chr12:123998884..124001416-chr12:124016546..124018370,2	K562	blood:
12	chr12:124008463..124013124-chr12:124014349..124019990,8	MCF-7	breast:
13	chr12:124006455..124008310-chr12:124016022..124017705,2	K562	blood:
14	chr12:123873494..123875550-chr12:124015653..124017169,2	MCF-7	breast:
15	chr12:124015709..124018064-chr12:124066858..124069100,3	MCF-7	breast:
16	chr12:124017444..124019100-chr12:124084646..124086674,2	MCF-7	breast:
17	chr12:124015786..124020200-chr12:124020787..124024805,6	K562	blood:
18	chr12:124007811..124010230-chr12:124011879..124014265,2	MCF-7	breast:
19	chr12:124014934..124016748-chr12:124100287..124103243,2	MCF-7	breast:
20	chr12:123997284..124000079-chr12:124017073..124019484,2	MCF-7	breast:
21	chr12:124016749..124018606-chr12:124069216..124071514,2	K562	blood:
22	chr12:124011402..124015187-chr12:124015616..124018872,7	K562	blood:
23	chr12:123871385..123875741-chr12:124017374..124019532,6	MCF-7	breast:
24	chr12:123753293..123757508-chr12:124015727..124020202,5	K562	blood:

No data

Variant related genes	Relation type
MIR3908	TF binding region
MIR3908	CpG island
ENSG00000184209	chromatin interactions
ENSG00000247373	chromatin interactions
ENSG00000206897	chromatin interactions
ENSG00000188026	chromatin interactions
ENSG00000111364	chromatin interactions
ENSG00000266655	chromatin interactions
ENSG00000183955	chromatin interactions
ENSG00000086598	chromatin interactions
ENSG00000111328	chromatin interactions

Extended variants
information (count: 179 )
Associated
traits (count: 71 )

Variant overlapped rSNPs/rCNVs (count:179 , 50 per page) page: 1 2 3 4

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs28375403	chr12:124012974-124012975	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs201808437	chr12:124012976-124012977	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs566728694	chr12:124012980-124012981	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs201546898	chr12:124012981-124012982	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs181961710	chr12:124012998-124012999	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs575996167	chr12:124013061-124013062	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs376550222	chr12:124013067-124013068	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs184771500	chr12:124013075-124013076	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs61953541	chr12:124013099-124013100	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs61953542	chr12:124013113-124013114	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs189025006	chr12:124013119-124013120	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs28450070	chr12:124013120-124013121	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs111547214	chr12:124013123-124013124	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs186162497	chr12:124013165-124013166	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs191609840	chr12:124013176-124013177	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs181691133	chr12:124013196-124013197	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs28580741	chr12:124013216-124013217	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs143928387	chr12:124013220-124013221	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	mRNA abundance
19	rs186225286	chr12:124013223-124013224	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs529540344	chr12:124013239-124013240	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs4930717	chr12:124013249-124013250	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs61953543	chr12:124013252-124013253	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs28741988	chr12:124013264-124013265	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
24	rs4930716	chr12:124013306-124013307	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
25	rs190950951	chr12:124013326-124013327	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs114801958	chr12:124013328-124013329	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs200540666	chr12:124013333-124013334	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs566629093	chr12:124013387-124013388	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs1057879	chr12:124013406-124013407	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
30	rs567650298	chr12:124013414-124013415	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs535067947	chr12:124013416-124013417	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs553691494	chr12:124013417-124013418	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs558389683	chr12:124013440-124013441	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs375436603	chr12:124013445-124013446	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs183287151	chr12:124013479-124013480	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs201610112	chr12:124013582-124013583	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs558061835	chr12:124013593-124013594	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs142606917	chr12:124013674-124013675	Weak transcription ZNF genes & repeats Strong transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs543440652	chr12:124013675-124013676	Weak transcription ZNF genes & repeats Strong transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs561679556	chr12:124013704-124013705	Weak transcription ZNF genes & repeats Strong transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs187956327	chr12:124013809-124013810	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs541086827	chr12:124013871-124013872	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs571703820	chr12:124013929-124013930	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs113246895	chr12:124013942-124013943	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs551693906	chr12:124013968-124013969	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs570006365	chr12:124013969-124013970	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs530857620	chr12:124014008-124014009	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs190625554	chr12:124014025-124014026	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs28535055	chr12:124014073-124014074	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs116263861	chr12:124014116-124014117	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:71)

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
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	16397240	CNVD
Breast cancer	17133270	CNVD
Breast cancer	17603634	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
Medulloblastoma	16783165	CNVD
Breast cancer	21806811	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Prostate cancer	18632612	CNVD
Myelofibrosis	22110671	CNVD
Beckwith-Wiedemann syndrome	20648245	CNVD
Developmental delay	21457577	CNVD
dysmorphic	21457577	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Olfactory neuroblastoma	18408657	CNVD
Chordoma	18071362	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:485 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:123970000-124016400	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
2	chr12:123994400-124016200	Weak transcription	Primary hematopoietic stem cells	blood
3	chr12:123994600-124016200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
4	chr12:123995200-124016400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
5	chr12:123999200-124015800	Weak transcription	Primary T helper cells PMA-I stimulated	--
6	chr12:123999400-124016400	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
7	chr12:124000600-124015000	Strong transcription	Primary neutrophils fromperipheralblood	blood
8	chr12:124001000-124016400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
9	chr12:124001200-124017400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
10	chr12:124001400-124017400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
11	chr12:124002000-124016800	Weak transcription	Rectal Mucosa Donor 29	rectum
12	chr12:124003000-124015400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
13	chr12:124004600-124016800	Weak transcription	Stomach Mucosa	stomach
14	chr12:124004800-124014600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
15	chr12:124004800-124016600	Weak transcription	Rectal Mucosa Donor 31	rectum
16	chr12:124005600-124015200	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
17	chr12:124005600-124016000	Weak transcription	Primary T helper cells fromperipheralblood	blood
18	chr12:124005600-124016400	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
19	chr12:124005600-124016400	Weak transcription	Duodenum Mucosa	Duodenum
20	chr12:124005800-124015800	Weak transcription	NHDF-Ad	bronchial
21	chr12:124005800-124016400	Weak transcription	Sigmoid Colon	Sigmoid Colon
22	chr12:124005800-124016600	Weak transcription	Fetal Kidney	kidney
23	chr12:124006000-124015000	Strong transcription	Fetal Muscle Leg	muscle
24	chr12:124006000-124015400	Weak transcription	Fetal Brain Male	brain
25	chr12:124006200-124017600	Weak transcription	Small Intestine	intestine
26	chr12:124006800-124016800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
27	chr12:124007200-124016600	Weak transcription	Primary T cells from cord blood	blood
28	chr12:124007800-124015200	Weak transcription	HUVEC	blood vessel
29	chr12:124007800-124016400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
30	chr12:124007800-124016600	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
31	chr12:124007800-124017000	Weak transcription	HUES48 Cell Line	embryonic stem cell
32	chr12:124007800-124017400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
33	chr12:124008000-124014400	Weak transcription	HSMM	muscle
34	chr12:124008000-124015400	Weak transcription	Rectal Smooth Muscle	rectum
35	chr12:124008000-124016000	Weak transcription	Hela-S3	cervix
36	chr12:124008000-124016400	Weak transcription	Dnd41	blood
37	chr12:124008000-124017000	Weak transcription	HUES64 Cell Line	embryonic stem cell
38	chr12:124008000-124017400	Weak transcription	H1 Cell Line	embryonic stem cell
39	chr12:124008200-124014200	Weak transcription	NHLF	lung
40	chr12:124008200-124015200	Weak transcription	Pancreas	Pancrea
41	chr12:124008200-124016600	Weak transcription	Primary T cells fromperipheralblood	blood
42	chr12:124008200-124017200	Weak transcription	H9 Cell Line	embryonic stem cell
43	chr12:124008400-124016600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
44	chr12:124008400-124017400	Weak transcription	Gastric	stomach
45	chr12:124008600-124015200	Weak transcription	Muscle Satellite Cultured Cells	--
46	chr12:124008800-124015200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
47	chr12:124009000-124013400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
48	chr12:124009000-124013400	Weak transcription	HUES6 Cell Line	embryonic stem cell
49	chr12:124009000-124015000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
50	chr12:124009000-124015400	Weak transcription	Brain Germinal Matrix	brain

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