Variant report

Variant	esv2751098
Chromosome Location	chr12:41082399-41180235
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:534)
CpG islands
(count:1283)
Chromatin interactive
region (count:8)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:534 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr12:41091506-41091600	K562	blood:	n/a	n/a
2	ATF2	chr12:41095495-41095972	GM12878	blood:	n/a	n/a
3	ATF2	chr12:41095553-41095922	GM12878	blood:	n/a	n/a
4	ATF3	chr12:41112137-41112996	A549	lung:	n/a	n/a
5	ATF3	chr12:41112133-41113026	A549	lung:	n/a	n/a
6	BACH1	chr12:41112882-41112949	H1-hESC	embryonic stem cell:	n/a	n/a
7	BATF	chr12:41095547-41095917	GM12878	blood:	n/a	n/a
8	BATF	chr12:41095607-41095850	GM12878	blood:	n/a	n/a
9	BCL11A	chr12:41095533-41095952	GM12878	blood:	n/a	n/a
10	BCL3	chr12:41112152-41113088	A549	lung:	n/a	n/a
11	BCL3	chr12:41112128-41113731	A549	lung:	n/a	n/a
12	BHLHE40	chr12:41145933-41146140	HepG2	liver:	n/a	n/a
13	BHLHE40	chr12:41112220-41112589	A549	lung:	n/a	n/a
14	CEBPB	chr12:41112226-41113067	A549	lung:	n/a	chr12:41112729-41112741
15	CEBPB	chr12:41084209-41084583	Hela-S3	cervix:	n/a	n/a
16	CEBPB	chr12:41112135-41113710	A549	lung:	n/a	chr12:41112729-41112741
17	CEBPB	chr12:41091537-41091915	A549	lung:	n/a	chr12:41091719-41091732 chr12:41091721-41091732 chr12:41091721-41091732
18	CEBPB	chr12:41164425-41164735	IMR90	lung:	n/a	chr12:41164561-41164572 chr12:41164561-41164574 chr12:41164562-41164573
19	CEBPB	chr12:41113250-41113604	A549	lung:	n/a	n/a
20	CEBPB	chr12:41084268-41084524	HepG2	liver:	n/a	n/a
21	CEBPB	chr12:41084151-41084563	ECC-1	luminal epithelium:	n/a	n/a
22	CEBPB	chr12:41084232-41084531	ECC-1	luminal epithelium:	n/a	n/a
23	CEBPB	chr12:41084252-41084501	MCF-7	breast:	n/a	n/a
24	CEBPB	chr12:41098485-41098906	A549	lung:	n/a	n/a
25	CEBPB	chr12:41084041-41084590	HCT-116	colon:	n/a	n/a
26	CEBPB	chr12:41091457-41091956	A549	lung:	n/a	chr12:41091719-41091732 chr12:41091721-41091732 chr12:41091721-41091732
27	CEBPB	chr12:41084203-41084776	A549	lung:	n/a	n/a
28	CEBPB	chr12:41111882-41113025	A549	lung:	n/a	chr12:41112729-41112741
29	CEBPB	chr12:41098585-41098918	Hela-S3	cervix:	n/a	n/a
30	CEBPB	chr12:41084053-41084569	A549	lung:	n/a	n/a
31	CEBPB	chr12:41116651-41116831	HepG2	liver:	n/a	chr12:41116736-41116747 chr12:41116736-41116749 chr12:41116737-41116748
32	CEBPB	chr12:41084425-41084448	K562	blood:	n/a	n/a
33	CEBPB	chr12:41084168-41084583	A549	lung:	n/a	n/a
34	CEBPB	chr12:41084159-41084588	HCT-116	colon:	n/a	n/a
35	CEBPB	chr12:41098590-41098896	A549	lung:	n/a	n/a
36	CEBPB	chr12:41164416-41164736	A549	lung:	n/a	chr12:41164561-41164572 chr12:41164561-41164574 chr12:41164562-41164573
37	CEBPB	chr12:41136111-41136121	H1-hESC	embryonic stem cell:	n/a	n/a
38	CEBPB	chr12:41135344-41135544	HepG2	liver:	n/a	chr12:41135458-41135471
39	CEBPB	chr12:41091532-41091950	A549	lung:	n/a	chr12:41091719-41091732 chr12:41091721-41091732 chr12:41091721-41091732
40	CEBPB	chr12:41164478-41164649	H1-hESC	embryonic stem cell:	n/a	chr12:41164561-41164572 chr12:41164561-41164574 chr12:41164562-41164573
41	CEBPB	chr12:41164468-41164721	HepG2	liver:	n/a	chr12:41164561-41164572 chr12:41164561-41164574 chr12:41164562-41164573
42	CEBPB	chr12:41164436-41164698	K562	blood:	n/a	chr12:41164561-41164572 chr12:41164561-41164574 chr12:41164562-41164573
43	CHD2	chr12:41086968-41087110	H1-hESC	embryonic stem cell:	n/a	n/a
44	CHD2	chr12:41085895-41086529	H1-hESC	embryonic stem cell:	n/a	n/a
45	CREB1	chr12:41112181-41112729	A549	lung:	n/a	n/a
46	CREB1	chr12:41112121-41112501	A549	lung:	n/a	n/a
47	CREB1	chr12:41085950-41086677	A549	lung:	n/a	n/a
48	CTBP2	chr12:41085963-41087461	H1-hESC	embryonic stem cell:	n/a	n/a
49	CTCF	chr12:41139260-41139410	BE2_C	brain:	n/a	n/a
50	CTCF	chr12:41139300-41139450	WERI-Rb-1	eye:	n/a	n/a

(count:1283 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:41086274-41086324	K562	blood:	n/a
2	chr12:41087252-41087302	SK-N-SH	brain:	n/a
3	chr12:41086274-41086324	K562	blood:	n/a
4	chr12:41087252-41087302	SK-N-SH	brain:	n/a
5	chr12:41086308-41086358	NHDF-neo	bronchial:	n/a
6	chr12:41086198-41086248	U87	brain:	n/a
7	chr12:41086879-41086929	ProgFib	skin:	n/a
8	chr12:41086879-41086929	PANC-1	pancreas:	n/a
9	chr12:41086365-41086415	HRE	kidney:	n/a
10	chr12:41085901-41085951	HL-60	blood:	n/a
11	chr12:41086274-41086324	AG10803	skin:	n/a
12	chr12:41086277-41086327	Hela-S3	cervix:	n/a
13	chr12:41086800-41086850	GM06990	blood:	n/a
14	chr12:41087101-41087151	Hepatocyte	liver:	n/a
15	chr12:41085901-41085951	HCPEpiC	choroid plexus:	n/a
16	chr12:41087520-41087570	AG04450	lung:	fetal
17	chr12:41086274-41086324	BE2_C	brain:	n/a
18	chr12:41086680-41086730	HCM	heart:	n/a
19	chr12:41087092-41087142	IMR90	lung:	fetal
20	chr12:41086879-41086929	HAEpiC	amniotic membrane:	n/a
21	chr12:41086365-41086415	PFSK-1	brain:	n/a
22	chr12:41086680-41086730	HMEC	breast:	n/a
23	chr12:41086274-41086324	GM19239	blood:	n/a
24	chr12:41086365-41086415	IMR90	lung:	fetal
25	chr12:41087252-41087302	AG04449	skin:	fetal
26	chr12:41086274-41086324	HRPEpiC	eye:	n/a
27	chr12:41087101-41087151	NH-A	brain:	n/a
28	chr12:41087252-41087302	PrEC	prostate:	n/a
29	chr12:41087520-41087570	HEK293	kidney:	embryo
30	chr12:41085901-41085951	NHDF-neo	bronchial:	n/a
31	chr12:41086680-41086730	AG04450	lung:	fetal
32	chr12:41086879-41086929	CMK	blood:	n/a
33	chr12:41085286-41085336	LNCaP	prostate:	n/a
34	chr12:41086680-41086730	Hepatocyte	liver:	n/a
35	chr12:41087584-41087634	AG04449	skin:	fetal
36	chr12:41086282-41086332	GM12878	blood:	n/a
37	chr12:41086365-41086415	HRPEpiC	eye:	n/a
38	chr12:41087520-41087570	HNPCEpiC	eye:	n/a
39	chr12:41087101-41087151	SK-N-SH	brain:	n/a
40	chr12:41086308-41086358	ECC-1	luminal epithelium:	n/a
41	chr12:41086050-41086100	HRCEpiC	kidney:	n/a
42	chr12:41087092-41087142	U87	brain:	n/a
43	chr12:41086277-41086327	HAEpiC	amniotic membrane:	n/a
44	chr12:41085286-41085336	ProgFib	skin:	n/a
45	chr12:41087520-41087570	H1-hESC	embryonic stem cell:	embryo
46	chr12:41087584-41087634	SK-N-SH_RA	brain:	n/a
47	chr12:41086198-41086248	T-47D	breast:	n/a
48	chr12:41086274-41086324	HRCEpiC	kidney:	n/a
49	chr12:41087520-41087570	HRPEpiC	eye:	n/a
50	chr12:41087520-41087570	NHBE	bronchial:	n/a

(count:8 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:41154089..41156351-chr12:41156663..41158742,2	K562	blood:
2	chr12:41106289..41108607-chr12:41111961..41113819,2	K562	blood:
3	chr12:41151197..41153698-chr12:41160986..41163331,2	K562	blood:
4	chr12:41162174..41163889-chr12:41167656..41170084,3	K562	blood:
5	chr12:41106289..41108607-chr12:41111961..41113819,2	K562	blood:
6	chr12:41154089..41156351-chr12:41156663..41158742,2	K562	blood:
7	chr12:41162174..41163889-chr12:41167656..41170084,3	K562	blood:
8	chr12:41151197..41153698-chr12:41160986..41163331,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-MUC19-3	chr12:41122613-41123699	NONHSAT027743

No data

Variant related genes	Relation type
ENSG00000257680	TF binding region
CNTN1	TF binding region
ENSG00000257680	CpG island
CNTN1	CpG island

Extended variants
information (count: 3452 )
Associated
traits (count: 61 )

Variant overlapped rSNPs/rCNVs (count:3452 , 50 per page) page: 1 2 3 4 5 6 7 ... 70

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs935224	chr12:41082399-41082400	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs546561326	chr12:41082407-41082408	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs563657386	chr12:41082416-41082417	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs377136513	chr12:41082449-41082450	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs35159781	chr12:41082461-41082462	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs369123876	chr12:41082484-41082485	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs547918057	chr12:41082529-41082530	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs556802912	chr12:41082553-41082554	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs112990254	chr12:41082559-41082560	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs568720741	chr12:41082575-41082576	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs531651045	chr12:41082618-41082619	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs535993265	chr12:41082632-41082633	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs550130320	chr12:41082710-41082711	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs73108972	chr12:41082741-41082742	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs372214919	chr12:41082768-41082769	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs142577681	chr12:41082782-41082783	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs540298774	chr12:41082788-41082789	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs369043712	chr12:41082796-41082797	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs558933506	chr12:41082802-41082803	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs199793275	chr12:41082840-41082841	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs577277922	chr12:41082860-41082861	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs1444204	chr12:41082882-41082883	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs186298663	chr12:41082920-41082921	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs36065915	chr12:41082986-41082987	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs190134322	chr12:41082995-41082996	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs369366466	chr12:41083003-41083004	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs377161040	chr12:41083083-41083084	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs111456266	chr12:41083122-41083123	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs537276553	chr12:41083123-41083124	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs542400644	chr12:41083127-41083128	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs560854340	chr12:41083195-41083196	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs369178605	chr12:41083202-41083203	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs547612899	chr12:41083203-41083204	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs546348552	chr12:41083211-41083212	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs570926797	chr12:41083215-41083216	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs146010119	chr12:41083230-41083231	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs550462764	chr12:41083255-41083256	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs207472861	chr12:41083263-41083264	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs568804941	chr12:41083275-41083276	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs11177809	chr12:41083277-41083278	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
41	rs74936034	chr12:41083291-41083292	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs181320832	chr12:41083312-41083313	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs534318273	chr12:41083363-41083364	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs149336074	chr12:41083366-41083367	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs144672907	chr12:41083380-41083381	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs185061927	chr12:41083439-41083440	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs554283816	chr12:41083456-41083457	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs556936894	chr12:41083461-41083462	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs148509927	chr12:41083472-41083473	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs145397941	chr12:41083476-41083477	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:61)

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
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Ewing''s sarcoma	19144156	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:581 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:41081000-41085800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
2	chr12:41082000-41082400	Enhancers	Ovary	ovary
3	chr12:41082000-41082600	Enhancers	Brain Anterior Caudate	brain
4	chr12:41082000-41082600	Flanking Active TSS	A549	lung
5	chr12:41082200-41083200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
6	chr12:41082200-41085600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
7	chr12:41082400-41082600	Enhancers	HUES6 Cell Line	embryonic stem cell
8	chr12:41082400-41082600	Enhancers	Fetal Kidney	kidney
9	chr12:41082400-41084000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
10	chr12:41082400-41085800	Weak transcription	Ovary	ovary
11	chr12:41082600-41084000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
12	chr12:41082600-41084000	Enhancers	A549	lung
13	chr12:41083000-41085600	Enhancers	NHEK	skin
14	chr12:41083200-41084400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
15	chr12:41083200-41085600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
16	chr12:41083800-41086000	Enhancers	HMEC	breast
17	chr12:41084000-41084400	Flanking Active TSS	A549	lung
18	chr12:41084000-41085000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
19	chr12:41084000-41085000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
20	chr12:41084200-41084400	Enhancers	iPS-18 Cell Line	embryonic stem cell
21	chr12:41084400-41084800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
22	chr12:41084400-41085000	Active TSS	A549	lung
23	chr12:41084800-41085800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
24	chr12:41085000-41085400	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
25	chr12:41085000-41085400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
26	chr12:41085000-41085400	Enhancers	Brain Inferior Temporal Lobe	brain
27	chr12:41085000-41085800	Flanking Active TSS	A549	lung
28	chr12:41085000-41086000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
29	chr12:41085200-41085400	Flanking Bivalent TSS/Enh	Brain Hippocampus Middle	brain
30	chr12:41085200-41085600	Enhancers	Pancreatic Islets	Pancreatic Islet
31	chr12:41085200-41085800	Bivalent Enhancer	Fetal Heart	heart
32	chr12:41085400-41085600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
33	chr12:41085400-41085600	Bivalent Enhancer	Brain Hippocampus Middle	brain
34	chr12:41085400-41085800	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Female	--
35	chr12:41085400-41085800	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
36	chr12:41085400-41085800	Flanking Active TSS	Brain Anterior Caudate	brain
37	chr12:41085400-41086800	Active TSS	iPS-15b Cell Line	embryonic stem cell
38	chr12:41085400-41086800	Active TSS	Brain Inferior Temporal Lobe	brain
39	chr12:41085400-41087200	Active TSS	Brain Angular Gyrus	brain
40	chr12:41085600-41085800	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
41	chr12:41085600-41085800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
42	chr12:41085600-41085800	Flanking Active TSS	Duodenum Smooth Muscle	Duodenum
43	chr12:41085600-41085800	Bivalent Enhancer	Fetal Stomach	stomach
44	chr12:41085600-41085800	Active TSS	Rectal Smooth Muscle	rectum
45	chr12:41085600-41085800	Flanking Bivalent TSS/Enh	Stomach Smooth Muscle	stomach
46	chr12:41085600-41086000	Flanking Bivalent TSS/Enh	HUES64 Cell Line	embryonic stem cell
47	chr12:41085600-41086000	Flanking Bivalent TSS/Enh	Brain Hippocampus Middle	brain
48	chr12:41085600-41086200	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
49	chr12:41085600-41086200	Flanking Active TSS	Breast Myoepithelial Primary Cells	Breast
50	chr12:41085600-41086200	Active TSS	Brain Germinal Matrix	brain

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