Variant report

Variant	esv3357908
Chromosome Location	chr12:117097394-117099942
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CHD2	chr12:117097942-117097963	HepG2	liver:	n/a	n/a
2	EP300	chr12:117097490-117098091	SK-N-SH	brain:	n/a	n/a
3	FOS	chr12:117097576-117097890	MCF10A-Er-Src	breast:	n/a	chr12:117097687-117097699
4	FOS	chr12:117097671-117097916	MCF10A-Er-Src	breast:	n/a	chr12:117097687-117097699
5	FOS	chr12:117097582-117097904	MCF10A-Er-Src	breast:	n/a	chr12:117097687-117097699
6	FOSL1	chr12:117097385-117098098	HCT-116	colon:	n/a	chr12:117097687-117097699
7	FOSL1	chr12:117097410-117098142	HCT-116	colon:	n/a	chr12:117097687-117097699
8	FOSL2	chr12:117097497-117098068	SK-N-SH	brain:	n/a	chr12:117097687-117097699
9	FOSL2	chr12:117097546-117097940	SK-N-SH	brain:	n/a	chr12:117097687-117097699
10	GATA2	chr12:117097580-117098320	SH-SY5Y	brain:	n/a	chr12:117097749-117097756 chr12:117097747-117097757 chr12:117097749-117097756 chr12:117097749-117097756 chr12:117097744-117097760 chr12:117097747-117097756 chr12:117097742-117097763
11	GATA3	chr12:117097651-117097951	SH-SY5Y	brain:	n/a	chr12:117097749-117097756 chr12:117097747-117097757 chr12:117097749-117097756 chr12:117097749-117097756 chr12:117097744-117097760 chr12:117097747-117097756 chr12:117097742-117097763
12	GATA3	chr12:117097343-117098178	A549	lung:	n/a	chr12:117097749-117097756 chr12:117097747-117097757 chr12:117097749-117097756 chr12:117097749-117097756 chr12:117097744-117097760 chr12:117097747-117097756 chr12:117097742-117097763
13	GATA3	chr12:117097564-117098070	MCF-7	breast:	n/a	chr12:117097749-117097756 chr12:117097747-117097757 chr12:117097749-117097756 chr12:117097749-117097756 chr12:117097744-117097760 chr12:117097747-117097756 chr12:117097742-117097763
14	GATA3	chr12:117097418-117098218	MCF-7	breast:	n/a	chr12:117097749-117097756 chr12:117097747-117097757 chr12:117097749-117097756 chr12:117097749-117097756 chr12:117097744-117097760 chr12:117097747-117097756 chr12:117097742-117097763
15	GATA3	chr12:117097450-117098234	SK-N-SH	brain:	n/a	chr12:117097749-117097756 chr12:117097747-117097757 chr12:117097749-117097756 chr12:117097749-117097756 chr12:117097744-117097760 chr12:117097747-117097756 chr12:117097742-117097763
16	GATA3	chr12:117097408-117098192	MCF-7	breast:	n/a	chr12:117097749-117097756 chr12:117097747-117097757 chr12:117097749-117097756 chr12:117097749-117097756 chr12:117097744-117097760 chr12:117097747-117097756 chr12:117097742-117097763
17	GATA3	chr12:117097339-117098349	SK-N-SH	brain:	n/a	chr12:117097749-117097756 chr12:117097747-117097757 chr12:117097749-117097756 chr12:117097749-117097756 chr12:117097744-117097760 chr12:117097747-117097756 chr12:117097742-117097763
18	GATA3	chr12:117097638-117097958	T-47D	breast:	n/a	chr12:117097749-117097756 chr12:117097747-117097757 chr12:117097749-117097756 chr12:117097749-117097756 chr12:117097744-117097760 chr12:117097747-117097756 chr12:117097742-117097763
19	JUND	chr12:117097371-117097973	HCT-116	colon:	n/a	chr12:117097687-117097699
20	JUND	chr12:117097408-117098133	HCT-116	colon:	n/a	chr12:117097687-117097699
21	JUND	chr12:117097432-117098086	SK-N-SH	brain:	n/a	chr12:117097687-117097699
22	JUND	chr12:117097423-117098133	SK-N-SH	brain:	n/a	chr12:117097687-117097699
23	MAFF	chr12:117099176-117099373	HepG2	liver:	n/a	chr12:117099282-117099300
24	MAFK	chr12:117099021-117099222	HepG2	liver:	n/a	n/a
25	MAFK	chr12:117099036-117099236	HepG2	liver:	n/a	chr12:117099210-117099225
26	MAX	chr12:117099176-117099602	NB4	blood:	n/a	n/a
27	MAX	chr12:117099815-117101060	NB4	blood:	n/a	chr12:117100557-117100567 chr12:117100316-117100325 chr12:117100317-117100327
28	MYC	chr12:117099207-117100966	NB4	blood:	n/a	chr12:117100557-117100567 chr12:117100316-117100325 chr12:117100317-117100327
29	NFIC	chr12:117097348-117098166	SK-N-SH	brain:	n/a	n/a
30	NFIC	chr12:117097484-117098062	SK-N-SH	brain:	n/a	n/a
31	NFYB	chr12:117097671-117097920	Hela-S3	cervix:	n/a	n/a
32	NFYB	chr12:117099290-117099490	GM12878	blood:	n/a	n/a
33	NFYB	chr12:117099120-117099428	K562	blood:	n/a	n/a
34	NR2F2	chr12:117097462-117098071	MCF-7	breast:	n/a	n/a
35	NR2F2	chr12:117097513-117097973	MCF-7	breast:	n/a	n/a
36	PAX5	chr12:117097561-117097854	GM12878	blood:	n/a	chr12:117097704-117097722 chr12:117097706-117097723
37	PAX5	chr12:117097576-117097857	GM12878	blood:	n/a	chr12:117097704-117097722 chr12:117097706-117097723
38	PAX5	chr12:117097545-117097884	GM12878	blood:	n/a	chr12:117097704-117097722 chr12:117097706-117097723
39	PBX3	chr12:117097393-117098143	SK-N-SH	brain:	n/a	n/a
40	PBX3	chr12:117097495-117098122	SK-N-SH	brain:	n/a	n/a
41	POLR2A	chr12:117097516-117097950	PANC-1	pancreas:	n/a	n/a
42	POLR2A	chr12:117099162-117100993	HL-60	blood:	n/a	n/a
43	POLR2A	chr12:117097601-117097875	HCT-116	colon:	n/a	n/a
44	POLR2A	chr12:117099255-117099478	K562	blood:	n/a	n/a
45	POLR2A	chr12:117097599-117097947	SK-N-SH	brain:	n/a	n/a
46	POLR2A	chr12:117099086-117100951	HL-60	blood:	n/a	n/a
47	POLR2A	chr12:117099150-117100945	NB4	blood:	n/a	n/a
48	REST	chr12:117099268-117099686	HL-60	blood:	n/a	n/a
49	SIN3AK20	chr12:117097387-117098097	MCF-7	breast:	n/a	n/a
50	SP1	chr12:117097380-117098168	HCT-116	colon:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:117099435-117099485	NHDF-neo	bronchial:	n/a
2	chr12:117099435-117099485	HRE	kidney:	n/a
3	chr12:117098395-117098445	AG04449	skin:	fetal
4	chr12:117098395-117098445	SK-N-MC	brain:	n/a
5	chr12:117099208-117099258	Jurkat	blood:	n/a
6	chr12:117098877-117098927	HRE	kidney:	n/a
7	chr12:117098877-117098927	HNPCEpiC	eye:	n/a
8	chr12:117099208-117099258	HCPEpiC	choroid plexus:	n/a
9	chr12:117098395-117098445	NHDF-neo	bronchial:	n/a
10	chr12:117099208-117099258	K562	blood:	n/a
11	chr12:117098877-117098927	RPTEC	kidney:	n/a
12	chr12:117098877-117098927	AG04449	skin:	fetal
13	chr12:117098877-117098927	AG10803	skin:	n/a
14	chr12:117099435-117099485	AG04449	skin:	fetal
15	chr12:117099435-117099485	PANC-1	pancreas:	n/a
16	chr12:117098395-117098445	ovcar-3	ovarian:	n/a
17	chr12:117098877-117098927	GM19239	blood:	n/a
18	chr12:117099435-117099485	HAEpiC	amniotic membrane:	n/a
19	chr12:117098395-117098445	HL-60	blood:	n/a
20	chr12:117099435-117099485	MCF10A-Er-Src	breast:	n/a
21	chr12:117098395-117098445	Hepatocyte	liver:	n/a
22	chr12:117098395-117098445	K562	blood:	n/a
23	chr12:117098877-117098927	AG04450	lung:	fetal
24	chr12:117098877-117098927	SKMC	muscle:	n/a
25	chr12:117098877-117098927	SK-N-SH	brain:	n/a
26	chr12:117098395-117098445	SK-N-SH	brain:	n/a
27	chr12:117099208-117099258	ovcar-3	ovarian:	n/a
28	chr12:117098877-117098927	Hepatocyte	liver:	n/a
29	chr12:117099208-117099258	GM12891	blood:	n/a
30	chr12:117099208-117099258	HCF	heart:	n/a
31	chr12:117098877-117098927	HEEpiC	esophagus:	n/a
32	chr12:117098877-117098927	NHDF-neo	bronchial:	n/a
33	chr12:117099208-117099258	CMK	blood:	n/a
34	chr12:117099208-117099258	ProgFib	skin:	n/a
35	chr12:117099208-117099258	LNCaP	prostate:	n/a
36	chr12:117099208-117099258	PrEC	prostate:	n/a
37	chr12:117098877-117098927	IMR90	lung:	fetal
38	chr12:117099435-117099485	Caco-2	colon:	n/a
39	chr12:117099435-117099485	Hepatocyte	liver:	n/a
40	chr12:117098877-117098927	HL-60	blood:	n/a
41	chr12:117099208-117099258	BJ	skin:	n/a
42	chr12:117099435-117099485	AG09309	skin:	n/a
43	chr12:117099435-117099485	SKMC	muscle:	n/a
44	chr12:117099208-117099258	AG09309	skin:	n/a
45	chr12:117098877-117098927	HUVEC	blood vessel:	n/a
46	chr12:117098395-117098445	A549	lung:	n/a
47	chr12:117099435-117099485	SAEC	small airway:	n/a
48	chr12:117098395-117098445	T-47D	breast:	n/a
49	chr12:117098395-117098445	HepG2	liver:	n/a
50	chr12:117099435-117099485	HRCEpiC	kidney:	n/a

No.	Distal block	Cell Line	Cell type
1	chr12:117095945..117098090-chr12:117099384..117101804,2	K562	blood:
2	chr12:117099623..117100620-chr2:42587817..42588707,2	NB4	blood:
3	chr12:117094883..117097893-chr12:117100651..117103499,3	MCF-7	breast:

Variant related genes	Relation type
ENSG00000257883	TF binding region
ENSG00000257883	CpG island
ENSG00000257883	chromatin interactions
ENSG00000115944	chromatin interactions

Extended variants
information (count: 117 )
Associated
traits (count: 71 )

Variant overlapped rSNPs/rCNVs (count:117 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs34597623	chr12:117097416-117097417	Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs139452887	chr12:117097419-117097420	Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs542647261	chr12:117097453-117097454	Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs556155307	chr12:117097478-117097479	Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs576218911	chr12:117097480-117097481	Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs545060414	chr12:117097520-117097521	Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs117298581	chr12:117097534-117097535	Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs146775072	chr12:117097552-117097553	Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs368988056	chr12:117097588-117097589	Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs547847793	chr12:117097601-117097602	Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs373484912	chr12:117097605-117097606	Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs561250213	chr12:117097622-117097623	Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs183592941	chr12:117097624-117097625	Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs530291663	chr12:117097636-117097637	Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs558977439	chr12:117097638-117097639	Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs144146891	chr12:117097651-117097652	Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs113729101	chr12:117097731-117097732	Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs114705181	chr12:117097741-117097742	Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs11832667	chr12:117097748-117097749	Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs146430580	chr12:117097751-117097752	Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs11832684	chr12:117097805-117097806	Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs558627712	chr12:117097843-117097844	Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs148607216	chr12:117097849-117097850	Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs567575646	chr12:117097909-117097910	Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs188470852	chr12:117097959-117097960	Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs192825441	chr12:117097999-117098000	Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs76195175	chr12:117098016-117098017	Weak transcription Enhancers Bivalent Enhancer ZNF genes & repeats	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs544670058	chr12:117098028-117098029	Weak transcription Enhancers Bivalent Enhancer ZNF genes & repeats	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs558667904	chr12:117098107-117098108	Weak transcription Enhancers Bivalent Enhancer ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs571999794	chr12:117098140-117098141	Weak transcription Enhancers Bivalent Enhancer ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs142041883	chr12:117098147-117098148	Weak transcription Enhancers Bivalent Enhancer ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs78159832	chr12:117098157-117098158	Weak transcription Enhancers Bivalent Enhancer ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs530351100	chr12:117098191-117098192	Weak transcription Enhancers Bivalent Enhancer ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs151175611	chr12:117098222-117098223	Weak transcription Enhancers ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs532576132	chr12:117098228-117098229	Weak transcription Enhancers ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs10850696	chr12:117098365-117098366	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs11068131	chr12:117098376-117098377	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs35712592	chr12:117098398-117098399	Weak transcription Enhancers ZNF genes & repeats	CpG island	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs111901654	chr12:117098399-117098400	Weak transcription Enhancers ZNF genes & repeats	CpG island	1 gene(s)	Overlapped CNVs	n/a
40	rs111390875	chr12:117098403-117098404	Weak transcription ZNF genes & repeats Enhancers	CpG island	1 gene(s)	Overlapped CNVs	n/a
41	rs567440850	chr12:117098428-117098429	Weak transcription ZNF genes & repeats Enhancers	CpG island	1 gene(s)	Overlapped CNVs	n/a
42	rs536429000	chr12:117098484-117098485	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs141907864	chr12:117098493-117098494	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs569962376	chr12:117098499-117098500	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs538633179	chr12:117098546-117098547	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs58382373	chr12:117098551-117098552	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs572123341	chr12:117098558-117098559	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs138169429	chr12:117098559-117098560	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs61938476	chr12:117098560-117098561	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs543597724	chr12:117098563-117098564	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	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
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
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:145 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:117093800-117100600	Weak transcription	H9 Cell Line	embryonic stem cell
2	chr12:117094200-117098000	Weak transcription	Lung	lung
3	chr12:117095600-117098600	Enhancers	Fetal Thymus	thymus
4	chr12:117095800-117098200	Enhancers	Primary hematopoietic stem cells short term culture	blood
5	chr12:117095800-117098200	Enhancers	Placenta	Placenta
6	chr12:117095800-117098400	Enhancers	Fetal Brain Male	brain
7	chr12:117096200-117097800	Enhancers	Aorta	Aorta
8	chr12:117096200-117098200	Enhancers	Primary monocytes fromperipheralblood	blood
9	chr12:117096400-117100200	Weak transcription	Left Ventricle	heart
10	chr12:117096400-117100200	Weak transcription	Sigmoid Colon	Sigmoid Colon
11	chr12:117096600-117097400	Weak transcription	Gastric	stomach
12	chr12:117096600-117098000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
13	chr12:117096600-117098000	Enhancers	Fetal Muscle Leg	muscle
14	chr12:117096600-117099800	Weak transcription	Rectal Mucosa Donor 29	rectum
15	chr12:117096600-117100200	Weak transcription	HUES48 Cell Line	embryonic stem cell
16	chr12:117096600-117100200	Weak transcription	Brain Germinal Matrix	brain
17	chr12:117096600-117103200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
18	chr12:117096800-117097800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
19	chr12:117096800-117097800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
20	chr12:117096800-117097800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
21	chr12:117096800-117098000	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin03	Skin
22	chr12:117096800-117098000	Enhancers	Stomach Mucosa	stomach
23	chr12:117096800-117098000	Enhancers	Thymus	Thymus
24	chr12:117096800-117098200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
25	chr12:117096800-117098200	Enhancers	Ovary	ovary
26	chr12:117096800-117098200	Enhancers	Monocytes-CD14+_RO01746	blood
27	chr12:117096800-117098400	Enhancers	A549	lung
28	chr12:117096800-117098400	Enhancers	HepG2	liver
29	chr12:117096800-117099200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
30	chr12:117096800-117099800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
31	chr12:117096800-117099800	Weak transcription	Fetal Intestine Large	intestine
32	chr12:117096800-117099800	Weak transcription	Fetal Intestine Small	intestine
33	chr12:117096800-117100000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
34	chr12:117096800-117100000	Weak transcription	Brain Substantia Nigra	brain
35	chr12:117096800-117100200	Weak transcription	HUES64 Cell Line	embryonic stem cell
36	chr12:117096800-117100200	Weak transcription	Brain Cingulate Gyrus	brain
37	chr12:117096800-117100200	Weak transcription	Right Ventricle	heart
38	chr12:117096800-117100400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
39	chr12:117096800-117100400	Weak transcription	HUES6 Cell Line	embryonic stem cell
40	chr12:117096800-117100400	Weak transcription	Brain Anterior Caudate	brain
41	chr12:117096800-117100400	Weak transcription	HSMM	muscle
42	chr12:117096800-117100600	Weak transcription	H1 Cell Line	embryonic stem cell
43	chr12:117097000-117097400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
44	chr12:117097000-117097400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
45	chr12:117097000-117097400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
46	chr12:117097000-117097400	Weak transcription	Duodenum Mucosa	Duodenum
47	chr12:117097000-117097600	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
48	chr12:117097000-117098000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
49	chr12:117097000-117098000	Enhancers	Muscle Satellite Cultured Cells	--
50	chr12:117097000-117098000	Weak transcription	Brain Hippocampus Middle	brain

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