Variant report

Variant	nsv519344
Chromosome Location	chr12:124171903-124194438
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:116)
CpG islands
(count:61)
Chromatin interactive
region (count:25)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:116 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr12:124172426-124172866	GM12878	blood:	n/a	n/a
2	ATF2	chr12:124172381-124172960	GM12878	blood:	n/a	n/a
3	ATF3	chr12:124190540-124190739	K562	blood:	n/a	n/a
4	ATF3	chr12:124190442-124190745	K562	blood:	n/a	n/a
5	BATF	chr12:124172484-124172812	GM12878	blood:	n/a	n/a
6	BATF	chr12:124172432-124172890	GM12878	blood:	n/a	n/a
7	BCL11A	chr12:124172540-124172846	GM12878	blood:	n/a	n/a
8	BCL11A	chr12:124172504-124172853	GM12878	blood:	n/a	n/a
9	BCLAF1	chr12:124172411-124172914	GM12878	blood:	n/a	n/a
10	BHLHE40	chr12:124172483-124172783	GM12878	blood:	n/a	n/a
11	CEBPB	chr12:124188889-124189157	HepG2	liver:	n/a	n/a
12	CEBPB	chr12:124172369-124173000	GM12878	blood:	n/a	n/a
13	CEBPB	chr12:124188933-124189113	A549	lung:	n/a	n/a
14	CREB1	chr12:124172425-124172956	GM12878	blood:	n/a	n/a
15	CTCF	chr12:124181352-124181448	LNCaP	prostate:	n/a	n/a
16	CTCF	chr12:124181357-124181387	GM13976	blood:	n/a	n/a
17	CTCF	chr12:124181280-124181430	HEEpiC	esophagus:	n/a	n/a
18	CTCF	chr12:124181240-124181390	MCF-7	breast:	n/a	n/a
19	CTCF	chr12:124190880-124191030	A549	lung:	n/a	n/a
20	CTCF	chr12:124181373-124181452	LNCaP	prostate:	n/a	n/a
21	CTCF	chr12:124175496-124175550	Medullo	brain:	n/a	n/a
22	CTCF	chr12:124184800-124184950	GM12868	blood:	n/a	n/a
23	CUX1	chr12:124172514-124172772	GM12878	blood:	n/a	n/a
24	EBF1	chr12:124172593-124172777	GM12878	blood:	n/a	n/a
25	EP300	chr12:124172494-124172817	GM12878	blood:	n/a	n/a
26	EP300	chr12:124172448-124172831	GM12878	blood:	n/a	n/a
27	EP300	chr12:124180733-124181134	T-47D	breast:	n/a	n/a
28	EP300	chr12:124172513-124172817	GM12878	blood:	n/a	n/a
29	EP300	chr12:124172504-124172723	GM12878	blood:	n/a	n/a
30	ESR1	chr12:124176810-124177153	T-47D	breast:	n/a	chr12:124176957-124176974 chr12:124176956-124176973
31	ESR1	chr12:124176812-124177151	T-47D	breast:	n/a	chr12:124176957-124176974 chr12:124176956-124176973
32	ESR1	chr12:124176826-124177173	T-47D	breast:	n/a	chr12:124176957-124176974 chr12:124176956-124176973
33	ESR1	chr12:124180758-124181223	T-47D	breast:	n/a	n/a
34	ESR1	chr12:124176781-124177235	T-47D	breast:	n/a	chr12:124176957-124176974 chr12:124176956-124176973
35	FOS	chr12:124175068-124175378	MCF10A-Er-Src	breast:	n/a	n/a
36	FOS	chr12:124190575-124190667	MCF10A-Er-Src	breast:	n/a	n/a
37	FOS	chr12:124175216-124175388	MCF10A-Er-Src	breast:	n/a	n/a
38	FOS	chr12:124175152-124175403	MCF10A-Er-Src	breast:	n/a	n/a
39	FOXA1	chr12:124180757-124181463	T-47D	breast:	n/a	chr12:124181144-124181156
40	FOXA1	chr12:124180742-124181468	T-47D	breast:	n/a	chr12:124181144-124181156
41	FOXM1	chr12:124172373-124172979	GM12878	blood:	n/a	n/a
42	FOXM1	chr12:124172390-124172904	GM12878	blood:	n/a	n/a
43	GATA3	chr12:124180708-124181589	T-47D	breast:	n/a	n/a
44	GATA3	chr12:124180761-124181526	T-47D	breast:	n/a	n/a
45	IKZF1	chr12:124172394-124172815	GM12878	blood:	n/a	n/a
46	IRF1	chr12:124177359-124177430	K562	blood:	n/a	n/a
47	IRF4	chr12:124172367-124172902	GM12878	blood:	n/a	n/a
48	IRF4	chr12:124172401-124172883	GM12878	blood:	n/a	n/a
49	JUND	chr12:124180687-124181532	T-47D	breast:	n/a	n/a
50	JUND	chr12:124190429-124190726	K562	blood:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:124192819-124192869	PANC-1	pancreas:	n/a
2	chr12:124192819-124192869	NH-A	brain:	n/a
3	chr12:124192819-124192869	T-47D	breast:	n/a
4	chr12:124192819-124192869	CMK	blood:	n/a
5	chr12:124192819-124192869	HRPEpiC	eye:	n/a
6	chr12:124192819-124192869	HRCEpiC	kidney:	n/a
7	chr12:124192819-124192869	ProgFib	skin:	n/a
8	chr12:124192819-124192869	NHDF-neo	bronchial:	n/a
9	chr12:124192819-124192869	HEK293	kidney:	embryo
10	chr12:124192819-124192869	HEEpiC	esophagus:	n/a
11	chr12:124192819-124192869	GM12892	blood:	n/a
12	chr12:124192819-124192869	SK-N-MC	brain:	n/a
13	chr12:124192819-124192869	GM12878	blood:	n/a
14	chr12:124192819-124192869	AG04450	lung:	fetal
15	chr12:124192819-124192869	HCF	heart:	n/a
16	chr12:124192819-124192869	AoSMC	blood vessel:	n/a
17	chr12:124192819-124192869	HNPCEpiC	eye:	n/a
18	chr12:124192819-124192869	HCM	heart:	n/a
19	chr12:124192819-124192869	PFSK-1	brain:	n/a
20	chr12:124192819-124192869	Hela-S3	cervix:	n/a
21	chr12:124192819-124192869	SK-N-SH	brain:	n/a
22	chr12:124192819-124192869	Hepatocyte	liver:	n/a
23	chr12:124192819-124192869	GM06990	blood:	n/a
24	chr12:124192819-124192869	HPAEpiC	pulmonary alveolar:	n/a
25	chr12:124192819-124192869	AG04449	skin:	fetal
26	chr12:124192819-124192869	MCF-7	breast:	n/a
27	chr12:124192819-124192869	HIPEpiC	eye:	n/a
28	chr12:124192819-124192869	NB4	blood:	n/a
29	chr12:124192819-124192869	HL-60	blood:	n/a
30	chr12:124192819-124192869	BJ	skin:	n/a
31	chr12:124192819-124192869	SKMC	muscle:	n/a
32	chr12:124192819-124192869	HMEC	breast:	n/a
33	chr12:124192819-124192869	Jurkat	blood:	n/a
34	chr12:124192819-124192869	HAEpiC	amniotic membrane:	n/a
35	chr12:124192819-124192869	H1-hESC	embryonic stem cell:	embryo
36	chr12:124192819-124192869	A549	lung:	n/a
37	chr12:124192819-124192869	U87	brain:	n/a
38	chr12:124192819-124192869	LNCaP	prostate:	n/a
39	chr12:124192819-124192869	ECC-1	luminal epithelium:	n/a
40	chr12:124192819-124192869	NT2-D1	testis:	n/a
41	chr12:124192819-124192869	HCT-116	colon:	n/a
42	chr12:124192819-124192869	IMR90	lung:	fetal
43	chr12:124192819-124192869	GM19239	blood:	n/a
44	chr12:124192819-124192869	GM12891	blood:	n/a
45	chr12:124192819-124192869	Caco-2	colon:	n/a
46	chr12:124192819-124192869	NHBE	bronchial:	n/a
47	chr12:124192819-124192869	HUVEC	blood vessel:	n/a
48	chr12:124192819-124192869	BE2_C	brain:	n/a
49	chr12:124192819-124192869	AG10803	skin:	n/a
50	chr12:124192819-124192869	K562	blood:	n/a

(count:25 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:124176790..124178829-chr12:124179921..124182332,2	K562	blood:
2	chr12:124176790..124178829-chr12:124179921..124182332,2	K562	blood:
3	chr12:124180128..124181646-chr12:124198369..124200192,2	MCF-7	breast:
4	chr12:124188235..124191139-chr12:124193941..124195953,3	MCF-7	breast:
5	chr12:124190696..124192494-chr12:124194252..124196865,2	K562	blood:
6	chr12:124185982..124187602-chr12:124193943..124196577,2	K562	blood:
7	chr12:124157024..124160371-chr12:124188986..124191737,3	MCF-7	breast:
8	chr12:124116424..124121252-chr12:124194298..124198817,7	K562	blood:
9	chr12:124171218..124172882-chr12:124173161..124174693,2	K562	blood:
10	chr12:124173898..124176239-chr12:124177848..124179680,2	MCF-7	breast:
11	chr12:124190696..124192494-chr12:124194252..124196865,2	K562	blood:
12	chr12:124171218..124172882-chr12:124173161..124174693,2	K562	blood:
13	chr12:124187896..124189887-chr12:124195478..124197199,2	K562	blood:
14	chr12:124185897..124191093-chr12:124195290..124198994,7	MCF-7	breast:
15	chr12:124186888..124189233-chr12:124196275..124198488,2	MCF-7	breast:
16	chr12:124191295..124193347-chr12:124194777..124198625,4	MCF-7	breast:
17	chr12:124185982..124187602-chr12:124193943..124196577,2	K562	blood:
18	chr12:124181824..124184450-chr12:124186002..124188364,2	K562	blood:
19	chr12:124189784..124191716-chr12:124194882..124197193,2	K562	blood:
20	chr12:123716636..123719388-chr12:124194108..124196844,2	K562	blood:
21	chr12:123716636..123719469-chr12:124192807..124195608,2	K562	blood:
22	chr12:124177268..124179844-chr12:124184486..124185994,2	K562	blood:
23	chr12:124188235..124191139-chr12:124193941..124195953,3	MCF-7	breast:
24	chr12:124172137..124174302-chr12:124194954..124197751,2	MCF-7	breast:
25	chr12:124181824..124184450-chr12:124186002..124188364,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-EIF2B1-3	chr12:124192149-124192324	ENSG00000255839
2	lnc-EIF2B1-3	chr12:124192789-124192933	ENSG00000255839

No data

Variant related genes	Relation type
TCTN2	TF binding region
ENSG00000255839	TF binding region
ATP6V0A2	TF binding region
TCTN2	CpG island
ENSG00000255839	CpG island
ATP6V0A2	CpG island
ENSG00000185344	chromatin interactions
ENSG00000111358	chromatin interactions
ENSG00000168778	chromatin interactions
ENSG00000130921	chromatin interactions
ENSG00000051825	chromatin interactions
ENSG00000111361	chromatin interactions

Extended variants
information (count: 906 )
Associated
traits (count: 70 )

Variant overlapped rSNPs/rCNVs (count:906 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6488893	chr12:124171903-124171904	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs572445904	chr12:124171927-124171928	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs187388942	chr12:124171975-124171976	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs564530076	chr12:124172032-124172033	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs531805135	chr12:124172046-124172047	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs543570077	chr12:124172047-124172048	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs562246423	chr12:124172075-124172076	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs552715422	chr12:124172086-124172087	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs529286124	chr12:124172106-124172107	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs144861830	chr12:124172127-124172128	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs566760791	chr12:124172128-124172129	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs527591610	chr12:124172129-124172130	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs541497412	chr12:124172132-124172133	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs545559680	chr12:124172135-124172136	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs561985159	chr12:124172154-124172155	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs10600469	chr12:124172218-124172219	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs375989669	chr12:124172222-124172223	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs541174469	chr12:124172280-124172281	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs564282610	chr12:124172298-124172299	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs12829984	chr12:124172307-124172308	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
21	rs570575000	chr12:124172325-124172326	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs7301907	chr12:124172342-124172343	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
23	rs555970024	chr12:124172371-124172372	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs567842273	chr12:124172376-124172377	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs535073828	chr12:124172377-124172378	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs563004427	chr12:124172403-124172404	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs553362148	chr12:124172406-124172407	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs572359130	chr12:124172415-124172416	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs371216376	chr12:124172422-124172423	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs189828374	chr12:124172426-124172427	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs576547267	chr12:124172447-124172448	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs544025450	chr12:124172457-124172458	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs562162888	chr12:124172458-124172459	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs111776710	chr12:124172499-124172500	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs7298831	chr12:124172555-124172556	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
36	rs201395894	chr12:124172559-124172560	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs372823085	chr12:124172575-124172576	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs199903945	chr12:124172587-124172588	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs151318349	chr12:124172609-124172610	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs140814969	chr12:124172614-124172615	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs144567556	chr12:124172643-124172644	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs368789244	chr12:124172675-124172676	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs562351608	chr12:124172689-124172690	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs371804063	chr12:124172691-124172692	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs73418153	chr12:124172706-124172707	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs201322440	chr12:124172710-124172711	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs531383211	chr12:124172713-124172714	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs116845100	chr12:124172721-124172722	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs7313032	chr12:124172731-124172732	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
50	rs374056297	chr12:124172738-124172739	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:70)

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

Chromatin state (count:502 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:124156200-124182000	Weak transcription	Small Intestine	intestine
2	chr12:124156400-124196000	Weak transcription	HUES48 Cell Line	embryonic stem cell
3	chr12:124156400-124196000	Weak transcription	Thymus	Thymus
4	chr12:124156600-124173000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
5	chr12:124156600-124175800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr12:124156600-124176000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
7	chr12:124156600-124180600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
8	chr12:124156600-124189800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
9	chr12:124156600-124195600	Weak transcription	Esophagus	oesophagus
10	chr12:124156600-124195800	Weak transcription	H1 Cell Line	embryonic stem cell
11	chr12:124156600-124195800	Weak transcription	HUES6 Cell Line	embryonic stem cell
12	chr12:124156600-124196000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
13	chr12:124156600-124196000	Weak transcription	Primary T helper cells PMA-I stimulated	--
14	chr12:124156600-124196000	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
15	chr12:124156600-124196000	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
16	chr12:124156800-124174200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
17	chr12:124156800-124175200	Weak transcription	HMEC	breast
18	chr12:124156800-124175800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
19	chr12:124156800-124177000	Weak transcription	Muscle Satellite Cultured Cells	--
20	chr12:124156800-124177000	Weak transcription	Hela-S3	cervix
21	chr12:124156800-124180200	Weak transcription	Stomach Mucosa	stomach
22	chr12:124156800-124181000	Weak transcription	Primary B cells from peripheral blood	blood
23	chr12:124156800-124181000	Weak transcription	Pancreatic Islets	Pancreatic Islet
24	chr12:124156800-124184000	Weak transcription	HepG2	liver
25	chr12:124156800-124186600	Weak transcription	Rectal Mucosa Donor 31	rectum
26	chr12:124156800-124196000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
27	chr12:124156800-124196000	Weak transcription	HUVEC	blood vessel
28	chr12:124156800-124196200	Weak transcription	HSMM	muscle
29	chr12:124157000-124193000	Strong transcription	Fetal Stomach	stomach
30	chr12:124157000-124196000	Weak transcription	Fetal Heart	heart
31	chr12:124157000-124196000	Weak transcription	NH-A	brain
32	chr12:124158200-124176400	Strong transcription	Fetal Muscle Trunk	muscle
33	chr12:124158400-124193800	Strong transcription	Breast Myoepithelial Primary Cells	Breast
34	chr12:124159800-124183800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
35	chr12:124160000-124181400	Weak transcription	HUES64 Cell Line	embryonic stem cell
36	chr12:124160000-124184400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
37	chr12:124160000-124195600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
38	chr12:124160200-124175400	Weak transcription	Brain Angular Gyrus	brain
39	chr12:124160200-124180600	Weak transcription	Fetal Kidney	kidney
40	chr12:124160200-124191000	Weak transcription	Colonic Mucosa	Colon
41	chr12:124160200-124195800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
42	chr12:124160200-124196000	Weak transcription	Right Ventricle	heart
43	chr12:124160400-124181000	Weak transcription	NHDF-Ad	bronchial
44	chr12:124160800-124174800	Weak transcription	Skeletal Muscle Male	skeletal muscle
45	chr12:124160800-124181000	Weak transcription	Primary T cells from cord blood	blood
46	chr12:124160800-124182800	Weak transcription	Dnd41	blood
47	chr12:124161600-124196000	Weak transcription	Duodenum Mucosa	Duodenum
48	chr12:124161800-124175600	Weak transcription	Gastric	stomach
49	chr12:124161800-124180800	Weak transcription	Fetal Brain Male	brain
50	chr12:124161800-124183000	Weak transcription	Placenta	Placenta

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