Variant report

Variant	nsv973995
Chromosome Location	chr12:10754447-10758396
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:25)
CpG islands
(count:61)
Chromatin interactive
region (count:9)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

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

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	EP300	chr12:10755381-10755572	GM12878	blood:	n/a	n/a
2	POLR2A	chr12:10753120-10754858	K562	blood:	n/a	n/a
3	POLR2A	chr12:10755518-10755714	Hela-S3	cervix:	n/a	n/a
4	POLR2A	chr12:10755379-10755392	MCF10A-Er-Src	breast:	n/a	n/a
5	POLR2A	chr12:10754435-10754466	MCF10A-Er-Src	breast:	n/a	n/a
6	POLR2A	chr12:10758271-10758442	MCF10A-Er-Src	breast:	n/a	n/a
7	POLR2A	chr12:10757847-10757855	K562	blood:	n/a	n/a
8	POLR2A	chr12:10755951-10758931	K562	blood:	n/a	n/a
9	POLR2A	chr12:10754821-10754892	Hela-S3	cervix:	n/a	n/a
10	POLR2A	chr12:10756506-10756995	MCF10A-Er-Src	breast:	n/a	n/a
11	POLR2A	chr12:10757026-10757359	HepG2	liver:	n/a	n/a
12	POLR2A	chr12:10757337-10757470	MCF10A-Er-Src	breast:	n/a	n/a
13	POLR2A	chr12:10758166-10758239	MCF10A-Er-Src	breast:	n/a	n/a
14	POLR2A	chr12:10755539-10755574	MCF-7	breast:	n/a	n/a
15	POLR2A	chr12:10755474-10755544	H1-hESC	embryonic stem cell:	n/a	n/a
16	POLR2A	chr12:10757770-10758056	MCF10A-Er-Src	breast:	n/a	n/a
17	POLR2A	chr12:10757546-10757859	MCF10A-Er-Src	breast:	n/a	n/a
18	POLR2A	chr12:10757475-10757671	K562	blood:	n/a	n/a
19	POLR2A	chr12:10754778-10754861	MCF10A-Er-Src	breast:	n/a	n/a
20	POLR2A	chr12:10757058-10758446	Hela-S3	cervix:	n/a	n/a
21	RFX5	chr12:10756433-10756590	K562	blood:	n/a	n/a
22	RUNX3	chr12:10757950-10758256	GM12878	blood:	n/a	n/a
23	SPI1	chr12:10757779-10758378	GM12878	blood:	n/a	n/a
24	SPI1	chr12:10757915-10758201	GM12891	blood:	n/a	n/a
25	SPI1	chr12:10757916-10758196	GM12878	blood:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:10757054-10757104	AG04450	lung:	fetal
2	chr12:10757054-10757104	HNPCEpiC	eye:	n/a
3	chr12:10757054-10757104	HRPEpiC	eye:	n/a
4	chr12:10757054-10757104	RPTEC	kidney:	n/a
5	chr12:10757054-10757104	NHDF-neo	bronchial:	n/a
6	chr12:10757054-10757104	HPAEpiC	pulmonary alveolar:	n/a
7	chr12:10757054-10757104	HL-60	blood:	n/a
8	chr12:10757054-10757104	HRCEpiC	kidney:	n/a
9	chr12:10757054-10757104	U87	brain:	n/a
10	chr12:10757054-10757104	GM06990	blood:	n/a
11	chr12:10757054-10757104	GM12878	blood:	n/a
12	chr12:10757054-10757104	CMK	blood:	n/a
13	chr12:10757054-10757104	HEK293	kidney:	embryo
14	chr12:10757054-10757104	LNCaP	prostate:	n/a
15	chr12:10757054-10757104	NHBE	bronchial:	n/a
16	chr12:10757054-10757104	PrEC	prostate:	n/a
17	chr12:10757054-10757104	HepG2	liver:	n/a
18	chr12:10757054-10757104	MCF-7	breast:	n/a
19	chr12:10757054-10757104	AoSMC	blood vessel:	n/a
20	chr12:10757054-10757104	HRE	kidney:	n/a
21	chr12:10757054-10757104	HCF	heart:	n/a
22	chr12:10757054-10757104	HUVEC	blood vessel:	n/a
23	chr12:10757054-10757104	T-47D	breast:	n/a
24	chr12:10757054-10757104	HAEpiC	amniotic membrane:	n/a
25	chr12:10757054-10757104	A549	lung:	n/a
26	chr12:10757054-10757104	H1-hESC	embryonic stem cell:	embryo
27	chr12:10757054-10757104	HCPEpiC	choroid plexus:	n/a
28	chr12:10757054-10757104	ECC-1	luminal epithelium:	n/a
29	chr12:10757054-10757104	GM12892	blood:	n/a
30	chr12:10757054-10757104	SK-N-SH	brain:	n/a
31	chr12:10757054-10757104	IMR90	lung:	fetal
32	chr12:10757054-10757104	NT2-D1	testis:	n/a
33	chr12:10757054-10757104	SK-N-MC	brain:	n/a
34	chr12:10757054-10757104	SK-N-SH_RA	brain:	n/a
35	chr12:10757054-10757104	SKMC	muscle:	n/a
36	chr12:10757054-10757104	ProgFib	skin:	n/a
37	chr12:10757054-10757104	HCM	heart:	n/a
38	chr12:10757054-10757104	HEEpiC	esophagus:	n/a
39	chr12:10757054-10757104	BJ	skin:	n/a
40	chr12:10757054-10757104	BE2_C	brain:	n/a
41	chr12:10757054-10757104	AG10803	skin:	n/a
42	chr12:10757054-10757104	HMEC	breast:	n/a
43	chr12:10757054-10757104	AG04449	skin:	fetal
44	chr12:10757054-10757104	Jurkat	blood:	n/a
45	chr12:10757054-10757104	AG09319	gingival:	n/a
46	chr12:10757054-10757104	NB4	blood:	n/a
47	chr12:10757054-10757104	PFSK-1	brain:	n/a
48	chr12:10757054-10757104	MCF10A-Er-Src	breast:	n/a
49	chr12:10757054-10757104	HCT-116	colon:	n/a
50	chr12:10757054-10757104	PANC-1	pancreas:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr12:10756231..10758139-chr12:10758556..10760735,3	MCF-7	breast:
2	chr12:10757768..10761323-chr12:10763648..10767654,5	MCF-7	breast:
3	chr12:10743385..10746001-chr12:10752818..10754982,2	K562	blood:
4	chr12:10752498..10759716-chr12:10759735..10767266,16	K562	blood:
5	chr12:10753486..10755683-chr12:10758710..10760560,2	MCF-7	breast:
6	chr12:10750720..10754463-chr12:10754546..10757493,4	K562	blood:
7	chr12:10754715..10757719-chr12:10762132..10766161,5	MCF-7	breast:
8	chr12:10753471..10755289-chr12:10762745..10764723,2	MCF-7	breast:
9	chr12:10751953..10754714-chr12:10755292..10756829,2	MCF-7	breast:

No data

Variant related genes	Relation type
KLRAP1	TF binding region
KLRAP1	CpG island
ENSG00000111196	chromatin interactions
ENSG00000256667	chromatin interactions

Extended variants
information (count: 183 )
Associated
traits (count: 87 )

Variant overlapped rSNPs/rCNVs (count:183 , 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	rs531964704	chr12:10754449-10754450	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs113285303	chr12:10754468-10754469	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs142220401	chr12:10754514-10754515	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs564291932	chr12:10754544-10754545	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs372065556	chr12:10754548-10754549	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs78568450	chr12:10754558-10754559	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs540675840	chr12:10754582-10754583	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs147860414	chr12:10754599-10754600	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs377361498	chr12:10754604-10754605	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs529235695	chr12:10754628-10754629	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs139435526	chr12:10754636-10754637	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs562724893	chr12:10754638-10754639	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs11053877	chr12:10754656-10754657	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs375691682	chr12:10754662-10754663	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs368625870	chr12:10754678-10754679	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs145055014	chr12:10754702-10754703	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs571108444	chr12:10754707-10754708	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs533542209	chr12:10754739-10754740	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs547031929	chr12:10754760-10754761	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs61473048	chr12:10754761-10754762	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs3759266	chr12:10754772-10754773	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs192804543	chr12:10754794-10754795	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs115385932	chr12:10754809-10754810	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs575812762	chr12:10754824-10754825	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs537914384	chr12:10754843-10754844	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs140784648	chr12:10754864-10754865	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs4763208	chr12:10754888-10754889	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
28	rs150234700	chr12:10754918-10754919	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs145814820	chr12:10754948-10754949	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs74617225	chr12:10754967-10754968	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs148991756	chr12:10754971-10754972	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs562502759	chr12:10754972-10754973	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs531535577	chr12:10754993-10754994	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs112886059	chr12:10755057-10755058	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs59613394	chr12:10755156-10755157	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs527419386	chr12:10755191-10755192	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs546968130	chr12:10755194-10755195	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs557599748	chr12:10755197-10755198	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs138493598	chr12:10755215-10755216	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs567912773	chr12:10755216-10755217	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs549662677	chr12:10755235-10755236	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs576704715	chr12:10755270-10755271	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs569308038	chr12:10755280-10755281	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs73256090	chr12:10755281-10755282	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs73256092	chr12:10755298-10755299	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs553395836	chr12:10755300-10755301	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs142736676	chr12:10755348-10755349	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs550366780	chr12:10755376-10755377	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs368548535	chr12:10755377-10755378	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs554174624	chr12:10755383-10755384	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:87)

Disease	PMID	Source
Acute lymphoblastic leukemia	17690704	CNVD
Medulloblastoma	16968546	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Hepatocellular carcinoma	16750200	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
Acute lymphoblastic leukemia	21248843	CNVD
Ewing''s sarcoma	17952124	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Breast cancer	21858162	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21785460	CNVD
Myelodysplastic syndrome	21251322	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Breast cancer	21364760	CNVD
Breast cancer	21509527	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	21611746	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Myelofibrosis	22110671	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Squamous cell cancer	19607727	CNVD
Prostate cancer	16573809	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Glioblastoma multiforme	22286061	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Acute myeloid leukemia	17268525	CNVD
Acute monocytic leukemia	16498392	CNVD
Prostate cancer	16461572	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Breast cancer	17133270	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Lung adenocarcinoma	21935476	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:184 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:10725600-10765000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
2	chr12:10725800-10761400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
3	chr12:10726400-10759800	Weak transcription	NHLF	lung
4	chr12:10726800-10756600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
5	chr12:10730000-10762000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
6	chr12:10730600-10764800	Weak transcription	Lung	lung
7	chr12:10730800-10758400	Weak transcription	NHEK	skin
8	chr12:10731200-10756400	Weak transcription	Primary B cells from peripheral blood	blood
9	chr12:10731600-10760800	Weak transcription	Fetal Brain Female	brain
10	chr12:10732000-10759600	Weak transcription	Fetal Intestine Large	intestine
11	chr12:10732000-10759800	Weak transcription	Placenta Amnion	Placenta Amnion
12	chr12:10732200-10759600	Weak transcription	Left Ventricle	heart
13	chr12:10732200-10761400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
14	chr12:10732200-10764800	Weak transcription	Skeletal Muscle Male	skeletal muscle
15	chr12:10732400-10759600	Weak transcription	Colon Smooth Muscle	Colon
16	chr12:10732400-10764200	Weak transcription	Pancreas	Pancrea
17	chr12:10732600-10759600	Weak transcription	HMEC	breast
18	chr12:10732800-10759600	Weak transcription	Brain Hippocampus Middle	brain
19	chr12:10733400-10759600	Weak transcription	HUVEC	blood vessel
20	chr12:10733600-10759800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
21	chr12:10733800-10760000	Weak transcription	Fetal Brain Male	brain
22	chr12:10734000-10759400	Weak transcription	Fetal Lung	lung
23	chr12:10734000-10764000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
24	chr12:10734000-10764600	Weak transcription	Thymus	Thymus
25	chr12:10734200-10755200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
26	chr12:10734200-10757400	Weak transcription	Fetal Muscle Trunk	muscle
27	chr12:10734200-10759400	Weak transcription	H1 Cell Line	embryonic stem cell
28	chr12:10734200-10759400	Weak transcription	Duodenum Mucosa	Duodenum
29	chr12:10734200-10759400	Weak transcription	Rectal Mucosa Donor 31	rectum
30	chr12:10734200-10759600	Weak transcription	H9 Cell Line	embryonic stem cell
31	chr12:10734200-10762200	Weak transcription	Fetal Muscle Leg	muscle
32	chr12:10734200-10764000	Weak transcription	Fetal Stomach	stomach
33	chr12:10734400-10754600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
34	chr12:10734400-10756600	Weak transcription	Skeletal Muscle Female	skeletal muscle
35	chr12:10734400-10764600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
36	chr12:10735200-10759600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
37	chr12:10735200-10764600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
38	chr12:10735400-10764000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
39	chr12:10736400-10758600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
40	chr12:10736600-10756600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
41	chr12:10738800-10764000	Weak transcription	Fetal Intestine Small	intestine
42	chr12:10739400-10761400	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
43	chr12:10741600-10756600	Weak transcription	Brain Substantia Nigra	brain
44	chr12:10742000-10761200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
45	chr12:10742200-10755400	Weak transcription	Primary monocytes fromperipheralblood	blood
46	chr12:10742600-10757200	Weak transcription	NH-A	brain
47	chr12:10742600-10764600	Weak transcription	Small Intestine	intestine
48	chr12:10742800-10764800	Weak transcription	Psoas Muscle	Psoas
49	chr12:10743400-10759600	Weak transcription	Brain Angular Gyrus	brain
50	chr12:10743400-10759600	Weak transcription	Brain Anterior Caudate	brain

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