Variant report

Variant	nsv983461
Chromosome Location	chr12:42851064-42854179
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:45)
CpG islands
(count:427)
Chromatin interactive
region (count:2)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:45 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CTCF	chr12:42852420-42852570	GM12872	blood:	n/a	n/a
2	CTCF	chr12:42851240-42851390	SK-N-SH_RA	brain:	n/a	n/a
3	CTCF	chr12:42852420-42852645	K562	blood:	n/a	n/a
4	CTCF	chr12:42851080-42851230	HMF	breast:	n/a	n/a
5	CTCF	chr12:42852440-42852590	HMF	breast:	n/a	n/a
6	CTCF	chr12:42851080-42851230	RPTEC	kidney:	n/a	n/a
7	CTCF	chr12:42851080-42851230	HFF	foreskin:	n/a	n/a
8	CTCF	chr12:42852480-42852630	HCPEpiC	choroid plexus:	n/a	n/a
9	CTCF	chr12:42851120-42851270	HCPEpiC	choroid plexus:	n/a	n/a
10	CTCF	chr12:42851120-42851270	HCFaa	heart:	n/a	n/a
11	CTCF	chr12:42851160-42851310	HMF	breast:	n/a	n/a
12	CTCF	chr12:42852560-42852710	NB4	blood:	n/a	n/a
13	CTCF	chr12:42851200-42851350	HPAF	blood vessel:	n/a	n/a
14	CTCF	chr12:42852500-42852650	HRE	kidney:	n/a	n/a
15	CTCF	chr12:42851080-42851230	MCF-7	breast:	n/a	n/a
16	CTCF	chr12:42852540-42852690	AG04450	lung:	n/a	n/a
17	CTCF	chr12:42851205-42851251	HUVEC	blood vessel:	n/a	n/a
18	CTCF	chr12:42851120-42851270	HPF	lung:	n/a	n/a
19	CTCF	chr12:42852527-42852594	Medullo	brain:	n/a	n/a
20	CTCF	chr12:42852500-42852650	HEK293	kidney:	n/a	n/a
21	CTCF	chr12:42851160-42851310	BJ	skin:	n/a	n/a
22	GATA2	chr12:42852400-42852697	HUVEC	blood vessel:	n/a	n/a
23	GATA3	chr12:42851169-42851285	SH-SY5Y	brain:	n/a	n/a
24	GATA3	chr12:42852911-42853061	SH-SY5Y	brain:	n/a	n/a
25	JUN	chr12:42852466-42852722	K562	blood:	n/a	n/a
26	JUND	chr12:42854040-42854349	HepG2	liver:	n/a	n/a
27	POLR2A	chr12:42851304-42851526	H1-hESC	embryonic stem cell:	n/a	n/a
28	POLR2A	chr12:42853177-42853194	H1-hESC	embryonic stem cell:	n/a	n/a
29	POLR2A	chr12:42851864-42852200	H1-neurons	neurons:	n/a	n/a
30	POLR2A	chr12:42853149-42853168	H1-hESC	embryonic stem cell:	n/a	n/a
31	POLR2A	chr12:42853073-42853249	H1-hESC	embryonic stem cell:	n/a	n/a
32	POLR2A	chr12:42853053-42853542	H1-hESC	embryonic stem cell:	n/a	n/a
33	POLR2A	chr12:42854008-42854088	HUVEC	blood vessel:	n/a	n/a
34	POLR2A	chr12:42853829-42853929	ProgFib	skin:	n/a	n/a
35	POLR2A	chr12:42851143-42851979	H1-hESC	embryonic stem cell:	n/a	n/a
36	POLR2A	chr12:42853854-42853888	HUVEC	blood vessel:	n/a	n/a
37	POLR2A	chr12:42851340-42851435	H1-hESC	embryonic stem cell:	n/a	n/a
38	POLR2A	chr12:42851481-42851582	MCF10A-Er-Src	breast:	n/a	n/a
39	POLR2A	chr12:42851457-42851459	H1-hESC	embryonic stem cell:	n/a	n/a
40	POLR2A	chr12:42852638-42852762	HUVEC	blood vessel:	n/a	n/a
41	POLR2A	chr12:42851022-42851276	HUVEC	blood vessel:	n/a	n/a
42	POLR2A	chr12:42851854-42851875	HUVEC	blood vessel:	n/a	n/a
43	RAD21	chr12:42851124-42851246	Hela-S3	cervix:	n/a	n/a
44	RAD21	chr12:42851136-42851283	SK-N-SH_RA	brain:	n/a	n/a
45	SMC3	chr12:42851153-42851257	Hela-S3	cervix:	n/a	n/a

(count:427 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:42854129-42854179	AG04450	lung:	fetal
2	chr12:42853904-42853954	IMR90	lung:	fetal
3	chr12:42853791-42853841	K562	blood:	n/a
4	chr12:42852913-42852963	HepG2	liver:	n/a
5	chr12:42854129-42854179	HEEpiC	esophagus:	n/a
6	chr12:42854080-42854130	A549	lung:	n/a
7	chr12:42853791-42853841	PANC-1	pancreas:	n/a
8	chr12:42853838-42853888	AoSMC	blood vessel:	n/a
9	chr12:42852913-42852963	HMEC	breast:	n/a
10	chr12:42853904-42853954	NHBE	bronchial:	n/a
11	chr12:42853904-42853954	ovcar-3	ovarian:	n/a
12	chr12:42853904-42853954	NH-A	brain:	n/a
13	chr12:42853838-42853888	BE2_C	brain:	n/a
14	chr12:42853791-42853841	ProgFib	skin:	n/a
15	chr12:42854080-42854130	IMR90	lung:	fetal
16	chr12:42854129-42854179	HepG2	liver:	n/a
17	chr12:42853791-42853841	SKMC	muscle:	n/a
18	chr12:42853904-42853954	H1-hESC	embryonic stem cell:	embryo
19	chr12:42853904-42853954	HMEC	breast:	n/a
20	chr12:42853904-42853954	AG04450	lung:	fetal
21	chr12:42852913-42852963	CMK	blood:	n/a
22	chr12:42854129-42854179	ovcar-3	ovarian:	n/a
23	chr12:42853838-42853888	HCT-116	colon:	n/a
24	chr12:42854080-42854130	Hela-S3	cervix:	n/a
25	chr12:42853838-42853888	SK-N-SH	brain:	n/a
26	chr12:42853791-42853841	NT2-D1	testis:	n/a
27	chr12:42853791-42853841	T-47D	breast:	n/a
28	chr12:42853838-42853888	GM12892	blood:	n/a
29	chr12:42853904-42853954	GM12878	blood:	n/a
30	chr12:42854080-42854130	GM12878	blood:	n/a
31	chr12:42854129-42854179	Hepatocyte	liver:	n/a
32	chr12:42853791-42853841	NHBE	bronchial:	n/a
33	chr12:42853838-42853888	NT2-D1	testis:	n/a
34	chr12:42853904-42853954	T-47D	breast:	n/a
35	chr12:42852913-42852963	HAEpiC	amniotic membrane:	n/a
36	chr12:42854129-42854179	T-47D	breast:	n/a
37	chr12:42853791-42853841	PrEC	prostate:	n/a
38	chr12:42854080-42854130	HCF	heart:	n/a
39	chr12:42854129-42854179	BJ	skin:	n/a
40	chr12:42854080-42854130	GM06990	blood:	n/a
41	chr12:42853838-42853888	MCF10A-Er-Src	breast:	n/a
42	chr12:42853904-42853954	SAEC	small airway:	n/a
43	chr12:42853988-42854038	NHBE	bronchial:	n/a
44	chr12:42854080-42854130	MCF10A-Er-Src	breast:	n/a
45	chr12:42853904-42853954	GM12891	blood:	n/a
46	chr12:42853838-42853888	IMR90	lung:	fetal
47	chr12:42852913-42852963	IMR90	lung:	fetal
48	chr12:42853904-42853954	GM06990	blood:	n/a
49	chr12:42853791-42853841	HRCEpiC	kidney:	n/a
50	chr12:42854080-42854130	K562	blood:	n/a

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr12:42853924..42855484-chr12:42857637..42859373,2	MCF-7	breast:
2	chr12:42851425..42853056-chr12:42860476..42863154,2	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000257225	TF binding region
ENSG00000257225	CpG island

Extended variants
information (count: 144 )
Associated
traits (count: 58 )

Variant overlapped rSNPs/rCNVs (count:144 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs556303664	chr12:42851094-42851095	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs574625750	chr12:42851110-42851111	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs191123770	chr12:42851218-42851219	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs560160405	chr12:42851247-42851248	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs117114511	chr12:42851256-42851257	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs546139033	chr12:42851271-42851272	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs142622811	chr12:42851272-42851273	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs145126550	chr12:42851280-42851281	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs564142136	chr12:42851304-42851305	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs370263993	chr12:42851308-42851309	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs73126453	chr12:42851318-42851319	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs117254564	chr12:42851330-42851331	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs150550386	chr12:42851334-42851335	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs77272764	chr12:42851354-42851355	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs146444442	chr12:42851364-42851365	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs139917735	chr12:42851374-42851375	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs566530237	chr12:42851375-42851376	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs182962207	chr12:42851401-42851402	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs143526581	chr12:42851403-42851404	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs61924366	chr12:42851409-42851410	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs146751664	chr12:42851422-42851423	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs2053943	chr12:42851438-42851439	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
23	rs369379331	chr12:42851499-42851500	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs574688977	chr12:42851511-42851512	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs139544221	chr12:42851520-42851521	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs144959796	chr12:42851546-42851547	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs111928412	chr12:42851562-42851563	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs553859437	chr12:42851565-42851566	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs572457462	chr12:42851646-42851647	Enhancers Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs149975921	chr12:42851678-42851679	Enhancers Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs540407499	chr12:42851708-42851709	Enhancers Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs564473531	chr12:42851713-42851714	Enhancers Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs190217366	chr12:42851719-42851720	Enhancers Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs145255245	chr12:42851737-42851738	Enhancers Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs532325264	chr12:42851747-42851748	Enhancers Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs530346632	chr12:42851750-42851751	Enhancers Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs548727706	chr12:42851786-42851787	Enhancers Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs566987905	chr12:42851797-42851798	Enhancers Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs562710168	chr12:42851802-42851803	Enhancers Weak transcription Genic enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs529920987	chr12:42851815-42851816	Enhancers Weak transcription Genic enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs548356397	chr12:42851819-42851820	Enhancers Weak transcription Genic enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs566464447	chr12:42851825-42851826	Enhancers Weak transcription Genic enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs527344391	chr12:42851878-42851879	Enhancers Weak transcription Genic enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs75928604	chr12:42851888-42851889	Enhancers Weak transcription Genic enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs559867316	chr12:42851917-42851918	Enhancers Weak transcription Genic enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs183227145	chr12:42852030-42852031	Enhancers Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs372755792	chr12:42852128-42852129	Enhancers Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs3168685	chr12:42852161-42852162	Enhancers Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs1051453	chr12:42852217-42852218	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
50	rs568374912	chr12:42852243-42852244	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:58)

Disease	PMID	Source
Chronic lymphocytic leukemia	21546498	CNVD
Seminomas	18059402	CNVD
Wilms tumour	21544195	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
Ewing''s sarcoma	21437220	CNVD
Testicular germ cell tumor	18059402	CNVD
Medulloblastoma	21979893	CNVD
Malaria	21533027	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Basal cell lymphoma	17053054	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Ewing''s sarcoma	17952124	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Neurodevelopmental disorder	22521361	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Renal cell carcinoma	18194544	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
Myelofibrosis	22110671	CNVD
Breast cancer	17603634	CNVD
Cancer	21183584	CNVD
Hirschsprung''s Disease	21712996	CNVD
Lissencephaly	21572526	CNVD
Lung cancer	18438408	CNVD
Acute myeloid leukemia	21251322	CNVD
small cell lung cancer	20016488	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Breast cancer	19602461	CNVD
Breast cancer	17899364	CNVD
Colorectal cancer	16272173	CNVD
Breast cancer	21364760	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Bipolar disorder	19114987	CNVD

Chromatin state (count:185 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:42816200-42858200	Weak transcription	Brain Inferior Temporal Lobe	brain
2	chr12:42816800-42862400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
3	chr12:42820000-42858200	Weak transcription	Gastric	stomach
4	chr12:42820200-42853000	Weak transcription	Fetal Heart	heart
5	chr12:42826400-42859000	Weak transcription	Fetal Brain Male	brain
6	chr12:42826600-42858200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr12:42831800-42876400	Weak transcription	Psoas Muscle	Psoas
8	chr12:42834200-42859600	Weak transcription	Brain Substantia Nigra	brain
9	chr12:42836000-42875800	Weak transcription	Stomach Mucosa	stomach
10	chr12:42836600-42853000	Weak transcription	H1 Cell Line	embryonic stem cell
11	chr12:42836800-42853000	Weak transcription	Right Ventricle	heart
12	chr12:42836800-42858800	Weak transcription	Brain Angular Gyrus	brain
13	chr12:42837000-42853200	Weak transcription	NHEK	skin
14	chr12:42837000-42853800	Weak transcription	Lung	lung
15	chr12:42837000-42858000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
16	chr12:42837000-42858000	Weak transcription	Aorta	Aorta
17	chr12:42837000-42858200	Weak transcription	Rectal Smooth Muscle	rectum
18	chr12:42837000-42868800	Weak transcription	Esophagus	oesophagus
19	chr12:42837200-42863200	Weak transcription	Rectal Mucosa Donor 31	rectum
20	chr12:42838400-42858000	Weak transcription	Placenta Amnion	Placenta Amnion
21	chr12:42838600-42853200	Weak transcription	Brain Anterior Caudate	brain
22	chr12:42839800-42853000	Weak transcription	Skeletal Muscle Female	skeletal muscle
23	chr12:42840000-42856400	Weak transcription	Fetal Intestine Small	intestine
24	chr12:42840400-42860800	Weak transcription	Colonic Mucosa	Colon
25	chr12:42840600-42852800	Weak transcription	Adipose Nuclei	Adipose
26	chr12:42840600-42858000	Weak transcription	Placenta	Placenta
27	chr12:42840600-42860000	Weak transcription	Brain Cingulate Gyrus	brain
28	chr12:42840800-42853200	Weak transcription	Duodenum Smooth Muscle	Duodenum
29	chr12:42840800-42853200	Weak transcription	Fetal Kidney	kidney
30	chr12:42840800-42858200	Weak transcription	Sigmoid Colon	Sigmoid Colon
31	chr12:42841000-42853000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
32	chr12:42841000-42853000	Weak transcription	Spleen	Spleen
33	chr12:42841000-42853600	Weak transcription	Colon Smooth Muscle	Colon
34	chr12:42841000-42858600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
35	chr12:42841200-42851800	Weak transcription	HMEC	breast
36	chr12:42841400-42856400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
37	chr12:42841400-42862000	Weak transcription	Cortex derived primary cultured neurospheres	brain
38	chr12:42841600-42858400	Weak transcription	Fetal Brain Female	brain
39	chr12:42841600-42862400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
40	chr12:42843000-42851400	Weak transcription	HSMM	muscle
41	chr12:42843000-42853000	Weak transcription	Rectal Mucosa Donor 29	rectum
42	chr12:42843000-42853200	Weak transcription	Duodenum Mucosa	Duodenum
43	chr12:42843000-42862400	Weak transcription	Fetal Thymus	thymus
44	chr12:42843200-42853200	Weak transcription	Ovary	ovary
45	chr12:42843200-42858200	Weak transcription	Primary monocytes fromperipheralblood	blood
46	chr12:42843200-42858200	Weak transcription	Pancreas	Pancrea
47	chr12:42843200-42862000	Weak transcription	Brain Hippocampus Middle	brain
48	chr12:42843600-42853000	Weak transcription	Stomach Smooth Muscle	stomach
49	chr12:42843600-42862400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
50	chr12:42844000-42853000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin

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