Variant report

Variant	nsv527641
Chromosome Location	chr12:1748834-1750047
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:11)
CpG islands
(count:184)
Chromatin interactive
region (count:4)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:11 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CTCF	chr12:1749823-1749863	H1-hESC	embryonic stem cell:	n/a	n/a
2	CTCF	chr12:1749780-1749930	HepG2	liver:	n/a	n/a
3	CTCF	chr12:1749855-1749869	MCF-7	breast:	n/a	n/a
4	CTCF	chr12:1749802-1749902	HepG2	liver:	n/a	n/a
5	CTCF	chr12:1749700-1749850	WERI-Rb-1	eye:	n/a	n/a
6	E2F6	chr12:1748572-1749248	H1-hESC	embryonic stem cell:	n/a	n/a
7	E2F6	chr12:1748675-1749158	H1-hESC	embryonic stem cell:	n/a	n/a
8	GABPA	chr12:1748671-1749019	H1-hESC	embryonic stem cell:	n/a	n/a
9	MAX	chr12:1748680-1749125	H1-hESC	embryonic stem cell:	n/a	n/a
10	MAX	chr12:1748692-1749124	H1-hESC	embryonic stem cell:	n/a	n/a
11	POLR2A	chr12:1749300-1749357	MCF10A-Er-Src	breast:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:1749013-1749063	HL-60	blood:	n/a
2	chr12:1749013-1749063	HL-60	blood:	n/a
3	chr12:1748816-1748866	HRPEpiC	eye:	n/a
4	chr12:1749159-1749209	ProgFib	skin:	n/a
5	chr12:1749013-1749063	ovcar-3	ovarian:	n/a
6	chr12:1748816-1748866	LNCaP	prostate:	n/a
7	chr12:1749013-1749063	Hela-S3	cervix:	n/a
8	chr12:1749013-1749063	Hepatocyte	liver:	n/a
9	chr12:1748816-1748866	SKMC	muscle:	n/a
10	chr12:1749159-1749209	NHBE	bronchial:	n/a
11	chr12:1748816-1748866	HCM	heart:	n/a
12	chr12:1749159-1749209	HIPEpiC	eye:	n/a
13	chr12:1749159-1749209	HRPEpiC	eye:	n/a
14	chr12:1748816-1748866	AG10803	skin:	n/a
15	chr12:1749013-1749063	AoSMC	blood vessel:	n/a
16	chr12:1749013-1749063	GM12878	blood:	n/a
17	chr12:1749159-1749209	U87	brain:	n/a
18	chr12:1748816-1748866	SK-N-SH_RA	brain:	n/a
19	chr12:1748816-1748866	Hela-S3	cervix:	n/a
20	chr12:1749013-1749063	SK-N-SH_RA	brain:	n/a
21	chr12:1749159-1749209	MCF-7	breast:	n/a
22	chr12:1749159-1749209	SK-N-SH	brain:	n/a
23	chr12:1749159-1749209	HUVEC	blood vessel:	n/a
24	chr12:1749159-1749209	HCPEpiC	choroid plexus:	n/a
25	chr12:1749013-1749063	H1-hESC	embryonic stem cell:	embryo
26	chr12:1748816-1748866	H1-hESC	embryonic stem cell:	embryo
27	chr12:1749159-1749209	AG09309	skin:	n/a
28	chr12:1748816-1748866	SAEC	small airway:	n/a
29	chr12:1749013-1749063	HRPEpiC	eye:	n/a
30	chr12:1748816-1748866	T-47D	breast:	n/a
31	chr12:1748816-1748866	HMEC	breast:	n/a
32	chr12:1749159-1749209	Caco-2	colon:	n/a
33	chr12:1749013-1749063	HCM	heart:	n/a
34	chr12:1749013-1749063	SKMC	muscle:	n/a
35	chr12:1749013-1749063	AG10803	skin:	n/a
36	chr12:1749159-1749209	GM12892	blood:	n/a
37	chr12:1749159-1749209	LNCaP	prostate:	n/a
38	chr12:1749013-1749063	SK-N-SH	brain:	n/a
39	chr12:1749159-1749209	GM12891	blood:	n/a
40	chr12:1749013-1749063	PANC-1	pancreas:	n/a
41	chr12:1749013-1749063	NHBE	bronchial:	n/a
42	chr12:1748816-1748866	AG09319	gingival:	n/a
43	chr12:1749159-1749209	HMEC	breast:	n/a
44	chr12:1749013-1749063	AG09319	gingival:	n/a
45	chr12:1748816-1748866	SK-N-SH	brain:	n/a
46	chr12:1748816-1748866	NHBE	bronchial:	n/a
47	chr12:1748816-1748866	HAEpiC	amniotic membrane:	n/a
48	chr12:1749013-1749063	PrEC	prostate:	n/a
49	chr12:1749013-1749063	NH-A	brain:	n/a
50	chr12:1749159-1749209	NH-A	brain:	n/a

(count:4 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:1739520..1741562-chr12:1747330..1749766,2	MCF-7	breast:
2	chr12:1746984..1749673-chr12:1753092..1755153,3	K562	blood:
3	chr12:1748743..1751681-chr12:1751691..1754305,2	MCF-7	breast:
4	chr12:1745580..1751053-chr12:1752530..1755627,4	K562	blood:

No data

Variant related genes	Relation type
WNT5B	TF binding region
WNT5B	CpG island
ENSG00000111186	chromatin interactions

Extended variants
information (count: 66 )
Associated
traits (count: 82 )

Variant overlapped rSNPs/rCNVs (count:66 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2270036	chr12:1748834-1748835	Weak transcription Strong transcription Bivalent/Poised TSS Enhancers Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs565275077	chr12:1748885-1748886	Weak transcription Strong transcription Bivalent/Poised TSS Enhancers Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs532334050	chr12:1748902-1748903	Weak transcription Strong transcription Bivalent/Poised TSS Enhancers Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs369974809	chr12:1748911-1748912	Weak transcription Strong transcription Bivalent/Poised TSS Enhancers Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs547393204	chr12:1748917-1748918	Weak transcription Strong transcription Bivalent/Poised TSS Enhancers Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs112329239	chr12:1748921-1748922	Weak transcription Strong transcription Bivalent/Poised TSS Enhancers Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs375562905	chr12:1748941-1748942	Weak transcription Strong transcription Bivalent/Poised TSS Enhancers Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs369464409	chr12:1748945-1748946	Weak transcription Strong transcription Bivalent/Poised TSS Enhancers Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs373230963	chr12:1748955-1748956	Weak transcription Strong transcription Bivalent/Poised TSS Enhancers Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs375865925	chr12:1748958-1748959	Weak transcription Strong transcription Bivalent/Poised TSS Enhancers Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs372237487	chr12:1748986-1748987	Weak transcription Strong transcription Bivalent/Poised TSS Enhancers Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs367954247	chr12:1748991-1748992	Weak transcription Strong transcription Bivalent/Poised TSS Enhancers Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs200664150	chr12:1749000-1749001	Weak transcription Strong transcription Bivalent/Poised TSS Enhancers Flanking Active TSS Genic enhancers Bivalent Enhancer Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs148300725	chr12:1749013-1749014	Weak transcription Strong transcription Enhancers Genic enhancers Bivalent Enhancer Active TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs551944178	chr12:1749031-1749032	Weak transcription Strong transcription Enhancers Genic enhancers Bivalent Enhancer Active TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs190705769	chr12:1749057-1749058	Weak transcription Strong transcription Enhancers Genic enhancers Bivalent Enhancer Active TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs141810959	chr12:1749078-1749079	Weak transcription Strong transcription Enhancers Genic enhancers Bivalent Enhancer Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs146279211	chr12:1749079-1749080	Weak transcription Strong transcription Enhancers Genic enhancers Bivalent Enhancer Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs376347332	chr12:1749101-1749102	Weak transcription Strong transcription Enhancers Genic enhancers Bivalent Enhancer Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs370999926	chr12:1749120-1749121	Weak transcription Strong transcription Enhancers Genic enhancers Bivalent Enhancer Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs267603398	chr12:1749128-1749129	Weak transcription Strong transcription Enhancers Genic enhancers Bivalent Enhancer Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs200126436	chr12:1749133-1749134	Weak transcription Strong transcription Enhancers Genic enhancers Bivalent Enhancer Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs374571917	chr12:1749182-1749183	Weak transcription Strong transcription Enhancers Genic enhancers Bivalent Enhancer Active TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs182947740	chr12:1749186-1749187	Weak transcription Strong transcription Enhancers Genic enhancers Bivalent Enhancer Active TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs187847828	chr12:1749211-1749212	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs576601161	chr12:1749249-1749250	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs544005506	chr12:1749256-1749257	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs565188672	chr12:1749325-1749326	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs576948333	chr12:1749339-1749340	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs572572572	chr12:1749346-1749347	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs190288220	chr12:1749351-1749352	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs75050430	chr12:1749353-1749354	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs182867219	chr12:1749361-1749362	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs10773974	chr12:1749372-1749373	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs558923471	chr12:1749379-1749380	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs113825664	chr12:1749391-1749392	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs7134091	chr12:1749461-1749462	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs28384807	chr12:1749473-1749474	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs142911236	chr12:1749502-1749503	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs572993040	chr12:1749554-1749555	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs530571650	chr12:1749564-1749565	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs147003268	chr12:1749566-1749567	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs570526548	chr12:1749570-1749571	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs374032066	chr12:1749589-1749590	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs546597293	chr12:1749610-1749611	Enhancers Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs568109383	chr12:1749645-1749646	Enhancers Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs536943697	chr12:1749680-1749681	Enhancers Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs7958302	chr12:1749765-1749766	Enhancers Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs148042051	chr12:1749827-1749828	Enhancers Strong transcription Weak transcription Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs2270037	chr12:1749841-1749842	Enhancers Strong transcription Weak transcription Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:82)

Disease	PMID	Source
Myelofibrosis	22110671	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Glaucoma	21310917	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Malignant peripheral nerve sheath tumor	19844265	CNVD
Squamous cell cancer	19607727	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Hepatocellular carcinoma	16750200	CNVD
Breast cancer	17133270	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Mental retardation	17847001	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
abnormal development	18461090	CNVD
Ovarian cancer	20844748	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Medulloblastoma	16968546	CNVD
Ovine squamous-cell carcinoma	17599052	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
Breast cancer	21364760	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Ewing''s sarcoma	17952124	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Breast cancer	21858162	CNVD
Breast cancer	21509527	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21785460	CNVD
Ovarian cancer	21720365	CNVD
Myelodysplastic syndrome	21251322	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Cancer	20164919	CNVD
Pancreatic cancer	17952125	CNVD
Lung adenocarcinoma	21935476	CNVD
Ovarian cancer	21781307	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:106 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:1739800-1753800	Weak transcription	Esophagus	oesophagus
2	chr12:1740000-1749000	Weak transcription	Ovary	ovary
3	chr12:1740600-1753400	Strong transcription	Osteobl	bone
4	chr12:1740600-1755000	Weak transcription	Spleen	Spleen
5	chr12:1740800-1751000	Weak transcription	Cortex derived primary cultured neurospheres	brain
6	chr12:1740800-1753200	Weak transcription	NH-A	brain
7	chr12:1740800-1753600	Weak transcription	Placenta	Placenta
8	chr12:1740800-1757400	Weak transcription	GM12878-XiMat	blood
9	chr12:1741000-1749200	Weak transcription	HSMMtube	muscle
10	chr12:1741400-1752800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
11	chr12:1742000-1753400	Weak transcription	NHEK	skin
12	chr12:1742200-1749400	Weak transcription	Stomach Smooth Muscle	stomach
13	chr12:1743000-1749400	Weak transcription	Fetal Lung	lung
14	chr12:1743600-1759000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
15	chr12:1743800-1749400	Weak transcription	Stomach Mucosa	stomach
16	chr12:1744000-1749200	Weak transcription	Muscle Satellite Cultured Cells	--
17	chr12:1744000-1753000	Weak transcription	Colon Smooth Muscle	Colon
18	chr12:1744000-1753200	Weak transcription	Colonic Mucosa	Colon
19	chr12:1744200-1749000	Weak transcription	Fetal Intestine Small	intestine
20	chr12:1744200-1751600	Weak transcription	Duodenum Mucosa	Duodenum
21	chr12:1744200-1753400	Weak transcription	Adipose Nuclei	Adipose
22	chr12:1744400-1752000	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
23	chr12:1744400-1753000	Weak transcription	Brain Inferior Temporal Lobe	brain
24	chr12:1744400-1753200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
25	chr12:1744400-1753200	Weak transcription	Duodenum Smooth Muscle	Duodenum
26	chr12:1744400-1759000	Weak transcription	Right Ventricle	heart
27	chr12:1744600-1753000	Weak transcription	Brain Cingulate Gyrus	brain
28	chr12:1744600-1753000	Weak transcription	Brain Substantia Nigra	brain
29	chr12:1744600-1758000	Weak transcription	HUES6 Cell Line	embryonic stem cell
30	chr12:1745000-1749000	Strong transcription	Foreskin Fibroblast Primary Cells skin02	Skin
31	chr12:1745000-1749200	Weak transcription	Fetal Brain Female	brain
32	chr12:1745000-1749600	Weak transcription	Brain Anterior Caudate	brain
33	chr12:1745000-1749800	Strong transcription	Fetal Muscle Trunk	muscle
34	chr12:1745000-1751400	Weak transcription	Rectal Mucosa Donor 29	rectum
35	chr12:1745000-1753200	Weak transcription	Brain Hippocampus Middle	brain
36	chr12:1745200-1750800	Strong transcription	Breast Myoepithelial Primary Cells	Breast
37	chr12:1745200-1751400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
38	chr12:1745600-1749200	Weak transcription	NHDF-Ad	bronchial
39	chr12:1745600-1753600	Weak transcription	Liver	Liver
40	chr12:1746200-1752000	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
41	chr12:1746400-1749600	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
42	chr12:1746600-1758000	Weak transcription	Placenta Amnion	Placenta Amnion
43	chr12:1747000-1749000	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
44	chr12:1747000-1750200	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
45	chr12:1747200-1749400	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
46	chr12:1747400-1750400	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
47	chr12:1747600-1752000	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
48	chr12:1747800-1754600	Weak transcription	Monocytes-CD14+_RO01746	blood
49	chr12:1747800-1755800	Strong transcription	Primary neutrophils fromperipheralblood	blood
50	chr12:1747800-1756000	Weak transcription	K562	blood

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links