Variant report

Variant	nsv899032
Chromosome Location	chr12:40735939-40827479
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:283)
CpG islands
(count:61)
Chromatin interactive
region (count:11)
LncRNA
region (count:28)
Mature miRNA
region (count: 0)
miRNA target
sites (count:2)

(count:283 , 50 per page) page: 1 2 3 4 5 6

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CEBPB	chr12:40748360-40748390	A549	lung:	n/a	n/a
2	CEBPB	chr12:40818598-40818846	IMR90	lung:	n/a	chr12:40818717-40818728
3	CEBPB	chr12:40818440-40818807	HepG2	liver:	n/a	chr12:40818529-40818540 chr12:40818717-40818728
4	CEBPB	chr12:40765714-40765997	A549	lung:	n/a	chr12:40765812-40765823
5	CEBPB	chr12:40791302-40791514	A549	lung:	n/a	n/a
6	CEBPB	chr12:40767587-40767770	HepG2	liver:	n/a	chr12:40767650-40767661
7	CEBPB	chr12:40818440-40818848	A549	lung:	n/a	chr12:40818529-40818540 chr12:40818717-40818728
8	CEBPB	chr12:40791310-40791585	HepG2	liver:	n/a	n/a
9	CEBPB	chr12:40765667-40765959	HepG2	liver:	n/a	chr12:40765812-40765823
10	CEBPB	chr12:40826439-40826590	A549	lung:	n/a	n/a
11	CEBPB	chr12:40755590-40755779	HepG2	liver:	n/a	n/a
12	CTCF	chr12:40768997-40769190	LNCaP	prostate:	n/a	n/a
13	CTCF	chr12:40768958-40769209	Gliobla	brain:	n/a	n/a
14	CTCF	chr12:40785540-40785690	AG04450	lung:	n/a	n/a
15	CTCF	chr12:40769040-40769190	BE2_C	brain:	n/a	n/a
16	CTCF	chr12:40769020-40769170	GM12870	blood:	n/a	n/a
17	CTCF	chr12:40769000-40769150	GM12874	blood:	n/a	n/a
18	CTCF	chr12:40769000-40769150	GM12865	blood:	n/a	n/a
19	CTCF	chr12:40768961-40769208	GM12878	blood:	n/a	n/a
20	CTCF	chr12:40769020-40769170	Hela-S3	cervix:	n/a	n/a
21	CTCF	chr12:40768980-40769130	HL-60	blood:	n/a	n/a
22	CTCF	chr12:40768680-40768830	HepG2	liver:	n/a	n/a
23	CTCF	chr12:40768940-40769090	HCM	heart:	n/a	n/a
24	CTCF	chr12:40769086-40769118	MCF-7	breast:	n/a	n/a
25	CTCF	chr12:40768865-40769225	MCF-7	breast:	n/a	n/a
26	CTCF	chr12:40769080-40769230	GM12878	blood:	n/a	n/a
27	CTCF	chr12:40769020-40769170	AG10803	skin:	n/a	n/a
28	CTCF	chr12:40768980-40769130	AG09319	gingival:	n/a	n/a
29	CTCF	chr12:40768980-40769130	HepG2	liver:	n/a	n/a
30	CTCF	chr12:40743500-40743650	GM12872	blood:	n/a	n/a
31	CTCF	chr12:40769006-40769212	GM13977	blood:	n/a	n/a
32	CTCF	chr12:40768980-40769130	WERI-Rb-1	eye:	n/a	n/a
33	CTCF	chr12:40768980-40769130	GM12878	blood:	n/a	n/a
34	CTCF	chr12:40768960-40769110	Caco-2	colon:	n/a	n/a
35	CTCF	chr12:40768980-40769130	GM12864	blood:	n/a	n/a
36	CTCF	chr12:40769120-40769270	HEEpiC	esophagus:	n/a	n/a
37	CTCF	chr12:40768940-40769090	HRPEpiC	eye:	n/a	n/a
38	CTCF	chr12:40769040-40769190	AG10803	skin:	n/a	n/a
39	CTCF	chr12:40768980-40769130	HRE	kidney:	n/a	n/a
40	CTCF	chr12:40768980-40769130	Caco-2	colon:	n/a	n/a
41	CTCF	chr12:40769040-40769190	HUVEC	blood vessel:	n/a	n/a
42	CTCF	chr12:40768963-40769213	MCF-7	breast:	n/a	n/a
43	CTCF	chr12:40823200-40823350	HPAF	blood vessel:	n/a	n/a
44	CTCF	chr12:40768940-40769090	HAc	cerebellar:	n/a	n/a
45	CTCF	chr12:40769020-40769170	HMF	breast:	n/a	n/a
46	CTCF	chr12:40769040-40769190	GM12874	blood:	n/a	n/a
47	CTCF	chr12:40769040-40769190	HVMF	connective:	n/a	n/a
48	CTCF	chr12:40768980-40769130	GM06990	blood:	n/a	n/a
49	CTCF	chr12:40768980-40769130	NHLF	lung:	n/a	n/a
50	CTCF	chr12:40769040-40769190	MCF-7	breast:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:40747204-40747254	GM12892	blood:	n/a
2	chr12:40747204-40747254	SAEC	small airway:	n/a
3	chr12:40747204-40747254	AoSMC	blood vessel:	n/a
4	chr12:40747204-40747254	AG10803	skin:	n/a
5	chr12:40747204-40747254	Jurkat	blood:	n/a
6	chr12:40747204-40747254	U87	brain:	n/a
7	chr12:40747204-40747254	AG04449	skin:	fetal
8	chr12:40747204-40747254	ovcar-3	ovarian:	n/a
9	chr12:40747204-40747254	HRE	kidney:	n/a
10	chr12:40747204-40747254	HCT-116	colon:	n/a
11	chr12:40747204-40747254	ProgFib	skin:	n/a
12	chr12:40747204-40747254	NHDF-neo	bronchial:	n/a
13	chr12:40747204-40747254	PFSK-1	brain:	n/a
14	chr12:40747204-40747254	H1-hESC	embryonic stem cell:	embryo
15	chr12:40747204-40747254	BE2_C	brain:	n/a
16	chr12:40747204-40747254	HAEpiC	amniotic membrane:	n/a
17	chr12:40747204-40747254	MCF-7	breast:	n/a
18	chr12:40747204-40747254	RPTEC	kidney:	n/a
19	chr12:40747204-40747254	HL-60	blood:	n/a
20	chr12:40747204-40747254	ECC-1	luminal epithelium:	n/a
21	chr12:40747204-40747254	MCF10A-Er-Src	breast:	n/a
22	chr12:40747204-40747254	AG09319	gingival:	n/a
23	chr12:40747204-40747254	Hepatocyte	liver:	n/a
24	chr12:40747204-40747254	NB4	blood:	n/a
25	chr12:40747204-40747254	K562	blood:	n/a
26	chr12:40747204-40747254	IMR90	lung:	fetal
27	chr12:40747204-40747254	BJ	skin:	n/a
28	chr12:40747204-40747254	A549	lung:	n/a
29	chr12:40747204-40747254	AG09309	skin:	n/a
30	chr12:40747204-40747254	GM12878	blood:	n/a
31	chr12:40747204-40747254	T-47D	breast:	n/a
32	chr12:40747204-40747254	LNCaP	prostate:	n/a
33	chr12:40747204-40747254	Caco-2	colon:	n/a
34	chr12:40747204-40747254	GM12891	blood:	n/a
35	chr12:40747204-40747254	PANC-1	pancreas:	n/a
36	chr12:40747204-40747254	NT2-D1	testis:	n/a
37	chr12:40747204-40747254	HCM	heart:	n/a
38	chr12:40747204-40747254	HUVEC	blood vessel:	n/a
39	chr12:40747204-40747254	CMK	blood:	n/a
40	chr12:40747204-40747254	Hela-S3	cervix:	n/a
41	chr12:40747204-40747254	SK-N-MC	brain:	n/a
42	chr12:40747204-40747254	SK-N-SH_RA	brain:	n/a
43	chr12:40747204-40747254	HCPEpiC	choroid plexus:	n/a
44	chr12:40747204-40747254	GM06990	blood:	n/a
45	chr12:40747204-40747254	HepG2	liver:	n/a
46	chr12:40747204-40747254	HEEpiC	esophagus:	n/a
47	chr12:40747204-40747254	HRCEpiC	kidney:	n/a
48	chr12:40747204-40747254	NH-A	brain:	n/a
49	chr12:40747204-40747254	AG04450	lung:	fetal
50	chr12:40747204-40747254	PrEC	prostate:	n/a

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr12:40802843..40805068-chr12:40806902..40808859,2	K562	blood:
2	chr12:40718929..40719819-chr12:40768166..40769419,3	MCF-7	breast:
3	chr12:40802843..40805068-chr12:40806902..40808859,2	K562	blood:
4	chr12:40802735..40804254-chr12:40811941..40814562,2	K562	blood:
5	12:40793507-40812339..12:40836437-40839614	H1-hESC	embryonic stem cell:	embryo
6	chr12:40803393..40806032-chr12:40844478..40846629,2	K562	blood:
7	chr12:40768243..40769926-chr12:40782774..40784277,2	K562	blood:
8	chr12:40768243..40769926-chr12:40782774..40784277,2	K562	blood:
9	chr12:40730058..40730795-chr12:40768301..40769589,4	MCF-7	breast:
10	12:40703633-40711447..12:40765226-40767074	GM12878	blood:
11	chr12:40730810..40731494-chr12:40768592..40769125,2	MCF-7	breast:

(count:28 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SLC2A13-3	chr12:40792362-40792466	ENSG00000258167.1
2	lnc-MUC19-1	chr12:40826429-40826566	NONHSAT027728
3	lnc-MUC19-1	chr12:40826180-40826264	NONHSAT027728
4	lnc-MUC19-1	chr12:40821772-40821895	NONHSAT027728
5	lnc-MUC19-1	chr12:40821176-40821298	NONHSAT027728
6	lnc-MUC19-1	chr12:40815015-40815125	NONHSAT027728
7	lnc-MUC19-1	chr12:40812976-40813035	NONHSAT027728
8	lnc-MUC19-1	chr12:40820209-40820419	NONHSAT027728
9	lnc-SLC2A13-3	chr12:40814022-40814113	ENSG00000258167.1
10	lnc-MUC19-1	chr12:40811932-40811982	NONHSAT027728
11	lnc-SLC2A13-3	chr12:40814022-40814118	XLOC_010054
12	lnc-SLC2A13-3	chr12:40814022-40814118	XLOC_010054
13	lnc-MUC19-1	chr12:40791681-40791713	NONHSAT027728
14	lnc-MUC19-1	chr12:40787197-40787301	NONHSAT027728
15	lnc-SLC2A13-3	chr12:40807837-40807921	XLOC_010054
16	lnc-SLC2A13-3	chr12:40814022-40814113	XLOC_010054
17	lnc-MUC19-1	chr12:40814009-40814237	NONHSAT027728
18	lnc-SLC2A13-3	chr12:40810103-40810240	XLOC_010054
19	lnc-MUC19-1	chr12:40805409-40805429	NONHSAT027728
20	lnc-MUC19-1	chr12:40815906-40816003	NONHSAT027728
21	lnc-SLC2A13-3	chr12:40810105-40810240	XLOC_010054
22	lnc-MUC19-1	chr12:40825428-40825520	NONHSAT027728
23	lnc-MUC19-1	chr12:40823344-40823479	NONHSAT027728
24	lnc-SLC2A13-3	chr12:40810105-40810240	XLOC_010054
25	lnc-SLC2A13-3	chr12:40789655-40789788	ENSG00000258167.1
26	lnc-MUC19-1	chr12:40815642-40815702	NONHSAT027728
27	lnc-SLC2A13-3	chr12:40789712-40789790	XLOC_010054
28	lnc-MUC19-1	chr12:40805835-40805984	NONHSAT027728

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	LRRK2	hsa-miR-205-5p	chr12:40761670-40761690
2	LRRK2	hsa-miR-205-5p	chr12:40761683-40761690

Variant related genes	Relation type
MUC19	TF binding region
MUC19	CpG island
ENSG00000188906	chromatin interactions
ENSG00000258167	chromatin interactions
ENSG00000205592	chromatin interactions
SEC23IP	miRNA target sites
STXBP3	miRNA target sites
MORF4L1	miRNA target sites
BLOC1S3	miRNA target sites
SLC25A37	miRNA target sites

Extended variants
information (count: 3161 )
Associated
traits (count: 58 )

Variant overlapped rSNPs/rCNVs (count:3161 , 50 per page) page: 1 2 3 4 5 6 7 ... 64

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10506155	chr12:40735939-40735940	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs574789922	chr12:40735953-40735954	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs184257931	chr12:40735973-40735974	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs7954061	chr12:40736010-40736011	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs554904148	chr12:40736012-40736013	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs538171494	chr12:40736027-40736028	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs7957151	chr12:40736043-40736044	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs574943489	chr12:40736077-40736078	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs11564174	chr12:40736111-40736112	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs367595415	chr12:40736181-40736182	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs369369244	chr12:40736237-40736238	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs919174	chr12:40736249-40736250	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs370623976	chr12:40736258-40736259	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs3065921	chr12:40736281-40736282	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs386376253	chr12:40736282-40736283	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs397837938	chr12:40736294-40736295	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs201293216	chr12:40736295-40736296	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs11176105	chr12:40736309-40736310	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs572295480	chr12:40736318-40736319	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs540258723	chr12:40736370-40736371	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs186902440	chr12:40736385-40736386	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs919175	chr12:40736405-40736406	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs192421526	chr12:40736432-40736433	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs562653427	chr12:40736449-40736450	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs142542728	chr12:40736527-40736528	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs548652034	chr12:40736590-40736591	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs566657073	chr12:40736591-40736592	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs527658698	chr12:40736612-40736613	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
29	rs552126894	chr12:40736644-40736645	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
30	rs184970662	chr12:40736645-40736646	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
31	rs532188704	chr12:40736673-40736674	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
32	rs538494167	chr12:40736692-40736693	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
33	rs556582337	chr12:40736768-40736769	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
34	rs541143678	chr12:40736770-40736771	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
35	rs1035812	chr12:40736782-40736783	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs376968935	chr12:40736832-40736833	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
37	rs150954733	chr12:40736885-40736886	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
38	rs554682181	chr12:40736905-40736906	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
39	rs188913936	chr12:40736943-40736944	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
40	rs1365764	chr12:40737002-40737003	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs58392855	chr12:40737059-40737060	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs67245647	chr12:40737060-40737061	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs397724721	chr12:40737067-40737068	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs17461964	chr12:40737075-40737076	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs192912223	chr12:40737080-40737081	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs544489024	chr12:40737096-40737097	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs10784518	chr12:40737115-40737116	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
48	rs4768231	chr12:40737183-40737184	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs114599803	chr12:40737202-40737203	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs559939527	chr12:40737216-40737217	Weak transcription Strong transcription	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
Cancer	20164919	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
Autism	20858243	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Breast cancer	19602461	CNVD
Breast cancer	17899364	CNVD
Cancer	20164920	CNVD
Colorectal cancer	16272173	CNVD
Breast cancer	21364760	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:40640600-40768200	Weak transcription	Pancreas	Pancrea
2	chr12:40656800-40746400	Strong transcription	Primary monocytes fromperipheralblood	blood
3	chr12:40674400-40760400	Weak transcription	Lung	lung
4	chr12:40681200-40763000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
5	chr12:40687200-40765000	Strong transcription	Primary neutrophils fromperipheralblood	blood
6	chr12:40712000-40736600	Weak transcription	Left Ventricle	heart
7	chr12:40712000-40743400	Weak transcription	Aorta	Aorta
8	chr12:40714200-40759200	Weak transcription	Duodenum Mucosa	Duodenum
9	chr12:40716800-40761600	Weak transcription	Fetal Kidney	kidney
10	chr12:40722400-40736200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
11	chr12:40722800-40755800	Weak transcription	Sigmoid Colon	Sigmoid Colon
12	chr12:40724600-40745400	Strong transcription	Monocytes-CD14+_RO01746	blood
13	chr12:40724800-40751000	Weak transcription	Brain Anterior Caudate	brain
14	chr12:40725000-40736200	Weak transcription	Brain Hippocampus Middle	brain
15	chr12:40725000-40739200	Strong transcription	Primary B cells from peripheral blood	blood
16	chr12:40725200-40761200	Weak transcription	Psoas Muscle	Psoas
17	chr12:40726200-40766600	Weak transcription	A549	lung
18	chr12:40726200-40767800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
19	chr12:40729800-40756000	Weak transcription	Skeletal Muscle Male	skeletal muscle
20	chr12:40730000-40745800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
21	chr12:40730000-40747000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
22	chr12:40730000-40760000	Weak transcription	Spleen	Spleen
23	chr12:40730400-40745400	Weak transcription	Skeletal Muscle Female	skeletal muscle
24	chr12:40732000-40745800	Weak transcription	Rectal Smooth Muscle	rectum
25	chr12:40732000-40757200	Weak transcription	Right Ventricle	heart
26	chr12:40732200-40743000	Weak transcription	Duodenum Smooth Muscle	Duodenum
27	chr12:40732800-40764000	Weak transcription	Colon Smooth Muscle	Colon
28	chr12:40733200-40757000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
29	chr12:40733400-40745600	Weak transcription	Adipose Nuclei	Adipose
30	chr12:40733600-40738400	Strong transcription	Primary B cells from cord blood	blood
31	chr12:40733600-40761400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
32	chr12:40733800-40737600	Strong transcription	Liver	Liver
33	chr12:40734000-40737000	Strong transcription	Ovary	ovary
34	chr12:40734600-40737000	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
35	chr12:40734600-40754200	Weak transcription	Esophagus	oesophagus
36	chr12:40735400-40745400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
37	chr12:40735600-40747000	Weak transcription	Brain Angular Gyrus	brain
38	chr12:40735800-40736200	Weak transcription	Stomach Smooth Muscle	stomach
39	chr12:40735800-40736200	Enhancers	GM12878-XiMat	blood
40	chr12:40736200-40737200	Strong transcription	Stomach Smooth Muscle	stomach
41	chr12:40736600-40737000	ZNF genes & repeats	Left Ventricle	heart
42	chr12:40737000-40742800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
43	chr12:40737000-40743600	Weak transcription	Ovary	ovary
44	chr12:40737000-40751600	Weak transcription	Left Ventricle	heart
45	chr12:40737200-40754000	Weak transcription	Stomach Smooth Muscle	stomach
46	chr12:40737600-40740400	Weak transcription	Liver	Liver
47	chr12:40738400-40740400	Weak transcription	Primary B cells from cord blood	blood
48	chr12:40739200-40740000	Weak transcription	Primary B cells from peripheral blood	blood
49	chr12:40740000-40741000	Strong transcription	Primary B cells from peripheral blood	blood
50	chr12:40740400-40744000	Strong transcription	Liver	Liver

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