Variant report

Variant	nsv832380
Chromosome Location	chr12:41132306-41323961
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr12:41300798-41301289	GM12878	blood:	n/a	n/a
2	ATF2	chr12:41213368-41213748	H1-hESC	embryonic stem cell:	n/a	n/a
3	ATF3	chr12:41300763-41301489	HCT-116	colon:	n/a	n/a
4	ATF3	chr12:41300812-41301420	HCT-116	colon:	n/a	n/a
5	BACH1	chr12:41223460-41223758	H1-hESC	embryonic stem cell:	n/a	chr12:41223582-41223596
6	BATF	chr12:41300829-41301349	GM12878	blood:	n/a	n/a
7	BATF	chr12:41300851-41301164	GM12878	blood:	n/a	n/a
8	BCL3	chr12:41300832-41301111	GM12878	blood:	n/a	n/a
9	BHLHE40	chr12:41145933-41146140	HepG2	liver:	n/a	n/a
10	CBX3	chr12:41300743-41301398	HCT-116	colon:	n/a	n/a
11	CBX3	chr12:41300680-41301419	HCT-116	colon:	n/a	n/a
12	CEBPB	chr12:41164436-41164698	K562	blood:	n/a	chr12:41164561-41164572 chr12:41164561-41164574 chr12:41164562-41164573
13	CEBPB	chr12:41300659-41301721	HCT-116	colon:	n/a	n/a
14	CEBPB	chr12:41300709-41301627	HCT-116	colon:	n/a	n/a
15	CEBPB	chr12:41183809-41184090	A549	lung:	n/a	chr12:41183962-41183975 chr12:41183963-41183974 chr12:41183962-41183973 chr12:41183961-41183978
16	CEBPB	chr12:41316813-41317030	HepG2	liver:	n/a	chr12:41316885-41316896
17	CEBPB	chr12:41164468-41164721	HepG2	liver:	n/a	chr12:41164561-41164572 chr12:41164561-41164574 chr12:41164562-41164573
18	CEBPB	chr12:41292125-41292356	K562	blood:	n/a	chr12:41292263-41292272 chr12:41292263-41292272 chr12:41292263-41292272 chr12:41292261-41292272 chr12:41292261-41292274 chr12:41292263-41292274 chr12:41292263-41292272
19	CEBPB	chr12:41223442-41223879	A549	lung:	n/a	n/a
20	CEBPB	chr12:41136111-41136121	H1-hESC	embryonic stem cell:	n/a	n/a
21	CEBPB	chr12:41316735-41316975	A549	lung:	n/a	chr12:41316885-41316896
22	CEBPB	chr12:41300760-41301507	Hela-S3	cervix:	n/a	n/a
23	CEBPB	chr12:41292102-41292510	IMR90	lung:	n/a	chr12:41292263-41292272 chr12:41292263-41292272 chr12:41292263-41292272 chr12:41292261-41292272 chr12:41292261-41292274 chr12:41292263-41292274 chr12:41292263-41292272
24	CEBPB	chr12:41164478-41164649	H1-hESC	embryonic stem cell:	n/a	chr12:41164561-41164572 chr12:41164561-41164574 chr12:41164562-41164573
25	CEBPB	chr12:41135344-41135544	HepG2	liver:	n/a	chr12:41135458-41135471
26	CEBPB	chr12:41164425-41164735	IMR90	lung:	n/a	chr12:41164561-41164572 chr12:41164561-41164574 chr12:41164562-41164573
27	CEBPB	chr12:41300754-41301591	A549	lung:	n/a	n/a
28	CEBPB	chr12:41300876-41301443	A549	lung:	n/a	n/a
29	CEBPB	chr12:41301195-41301363	HepG2	liver:	n/a	n/a
30	CEBPB	chr12:41292120-41292628	A549	lung:	n/a	chr12:41292263-41292272 chr12:41292263-41292272 chr12:41292263-41292272 chr12:41292261-41292272 chr12:41292261-41292274 chr12:41292263-41292274 chr12:41292263-41292272
31	CEBPB	chr12:41276729-41276868	H1-hESC	embryonic stem cell:	n/a	chr12:41276831-41276848 chr12:41276836-41276847 chr12:41276834-41276845
32	CEBPB	chr12:41316831-41316986	K562	blood:	n/a	chr12:41316885-41316896
33	CEBPB	chr12:41258061-41258367	IMR90	lung:	n/a	chr12:41258213-41258224
34	CEBPB	chr12:41164416-41164736	A549	lung:	n/a	chr12:41164561-41164572 chr12:41164561-41164574 chr12:41164562-41164573
35	CEBPB	chr12:41276690-41276993	IMR90	lung:	n/a	chr12:41276831-41276848 chr12:41276836-41276847 chr12:41276834-41276845
36	CEBPB	chr12:41276707-41277012	HepG2	liver:	n/a	chr12:41276831-41276848 chr12:41276836-41276847 chr12:41276834-41276845
37	CEBPB	chr12:41249636-41249878	A549	lung:	n/a	n/a
38	CEBPB	chr12:41223797-41223799	H1-hESC	embryonic stem cell:	n/a	n/a
39	CEBPB	chr12:41258094-41258328	HepG2	liver:	n/a	chr12:41258213-41258224
40	CEBPB	chr12:41276720-41276961	A549	lung:	n/a	chr12:41276831-41276848 chr12:41276836-41276847 chr12:41276834-41276845
41	CEBPB	chr12:41240244-41240257	K562	blood:	n/a	n/a
42	CEBPB	chr12:41183147-41183186	A549	lung:	n/a	n/a
43	CEBPB	chr12:41183832-41184117	HepG2	liver:	n/a	chr12:41183962-41183975 chr12:41183963-41183974 chr12:41183962-41183973 chr12:41183961-41183978
44	CEBPB	chr12:41292092-41292612	HepG2	liver:	n/a	chr12:41292263-41292272 chr12:41292263-41292272 chr12:41292263-41292272 chr12:41292261-41292272 chr12:41292261-41292274 chr12:41292263-41292274 chr12:41292263-41292272
45	CHD2	chr12:41213311-41213590	H1-hESC	embryonic stem cell:	n/a	n/a
46	CHD2	chr12:41301029-41301222	GM12878	blood:	n/a	n/a
47	CTBP2	chr12:41212956-41213785	H1-hESC	embryonic stem cell:	n/a	n/a
48	CTCF	chr12:41155980-41156130	HCT-116	colon:	n/a	n/a
49	CTCF	chr12:41156000-41156150	SK-N-SH_RA	brain:	n/a	n/a
50	CTCF	chr12:41139302-41139483	LNCaP	prostate:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:41221855-41221905	HPAEpiC	pulmonary alveolar:	n/a
2	chr12:41221689-41221739	HPAEpiC	pulmonary alveolar:	n/a
3	chr12:41289297-41289347	HIPEpiC	eye:	n/a
4	chr12:41323612-41323662	Jurkat	blood:	n/a
5	chr12:41221855-41221905	SKMC	muscle:	n/a
6	chr12:41289297-41289347	HEEpiC	esophagus:	n/a
7	chr12:41221639-41221689	HL-60	blood:	n/a
8	chr12:41323612-41323662	NHDF-neo	bronchial:	n/a
9	chr12:41221689-41221739	SK-N-SH_RA	brain:	n/a
10	chr12:41323612-41323662	HPAEpiC	pulmonary alveolar:	n/a
11	chr12:41221855-41221905	HCT-116	colon:	n/a
12	chr12:41221855-41221905	T-47D	breast:	n/a
13	chr12:41221639-41221689	AG10803	skin:	n/a
14	chr12:41221855-41221905	BE2_C	brain:	n/a
15	chr12:41289297-41289347	Jurkat	blood:	n/a
16	chr12:41289297-41289347	HPAEpiC	pulmonary alveolar:	n/a
17	chr12:41221689-41221739	HRE	kidney:	n/a
18	chr12:41289297-41289347	HCPEpiC	choroid plexus:	n/a
19	chr12:41289297-41289347	RPTEC	kidney:	n/a
20	chr12:41221855-41221905	PFSK-1	brain:	n/a
21	chr12:41323612-41323662	H1-hESC	embryonic stem cell:	embryo
22	chr12:41221689-41221739	GM12891	blood:	n/a
23	chr12:41221639-41221689	HNPCEpiC	eye:	n/a
24	chr12:41221689-41221739	HCM	heart:	n/a
25	chr12:41221639-41221689	SKMC	muscle:	n/a
26	chr12:41221639-41221689	HEEpiC	esophagus:	n/a
27	chr12:41221639-41221689	HRE	kidney:	n/a
28	chr12:41323612-41323662	PrEC	prostate:	n/a
29	chr12:41289297-41289347	GM19239	blood:	n/a
30	chr12:41221639-41221689	AG09319	gingival:	n/a
31	chr12:41289297-41289347	NH-A	brain:	n/a
32	chr12:41221639-41221689	PFSK-1	brain:	n/a
33	chr12:41289297-41289347	Hela-S3	cervix:	n/a
34	chr12:41221855-41221905	GM19239	blood:	n/a
35	chr12:41221689-41221739	T-47D	breast:	n/a
36	chr12:41221855-41221905	AG09319	gingival:	n/a
37	chr12:41221639-41221689	MCF10A-Er-Src	breast:	n/a
38	chr12:41221639-41221689	HRCEpiC	kidney:	n/a
39	chr12:41221689-41221739	Caco-2	colon:	n/a
40	chr12:41221855-41221905	HIPEpiC	eye:	n/a
41	chr12:41289297-41289347	SAEC	small airway:	n/a
42	chr12:41289297-41289347	SK-N-SH	brain:	n/a
43	chr12:41221689-41221739	K562	blood:	n/a
44	chr12:41221855-41221905	A549	lung:	n/a
45	chr12:41289297-41289347	SK-N-MC	brain:	n/a
46	chr12:41221639-41221689	BJ	skin:	n/a
47	chr12:41221855-41221905	HAEpiC	amniotic membrane:	n/a
48	chr12:41221855-41221905	HMEC	breast:	n/a
49	chr12:41323612-41323662	T-47D	breast:	n/a
50	chr12:41323612-41323662	AG04449	skin:	fetal

No.	Distal block	Cell Line	Cell type
1	chr12:41015843..41016729-chr12:41315089..41315598,2	K562	blood:
2	chr12:41154089..41156351-chr12:41156663..41158742,2	K562	blood:
3	chr12:41249860..41251480-chr12:41252962..41255382,2	K562	blood:
4	chr12:41266646..41269338-chr13:42807949..42810576,2	MCF-7	breast:
5	chr12:41249860..41251480-chr12:41252962..41255382,2	K562	blood:
6	chr12:41311476..41312055-chr19:35811147..35811765,2	MCF-7	breast:
7	chr12:41222882..41225557-chr7:143112465..143114503,2	MCF-7	breast:
8	chr12:41298926..41301018-chr12:41302618..41305586,2	K562	blood:
9	chr12:41154089..41156351-chr12:41156663..41158742,2	K562	blood:
10	chr12:41162174..41163889-chr12:41167656..41170084,3	K562	blood:
11	chr12:40719199..40719744-chr12:41315365..41315912,2	MCF-7	breast:
12	chr12:41151197..41153698-chr12:41160986..41163331,2	K562	blood:
13	chr12:41015832..41017042-chr12:41315031..41316480,11	MCF-7	breast:
14	chr12:41015662..41016670-chr12:41314832..41315906,5	MCF-7	breast:
15	chr12:41162174..41163889-chr12:41167656..41170084,3	K562	blood:
16	chr12:41298926..41301018-chr12:41302618..41305586,2	K562	blood:
17	chr12:41151197..41153698-chr12:41160986..41163331,2	K562	blood:
18	chr12:41227812..41228332-chr8:90860181..90861388,5	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-MUC19-5	chr12:41221897-41222103	NONHSAT027744

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

Extended variants
information (count: 6540 )
Associated
traits (count: 62 )

Variant overlapped rSNPs/rCNVs (count:6540 , 50 per page) page: 1 2 3 4 5 6 7 ... 131

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs201993013	chr12:41132349-41132350	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs543055897	chr12:41132379-41132380	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs561258969	chr12:41132447-41132448	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs528830039	chr12:41132454-41132455	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs370188096	chr12:41132469-41132470	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs546957467	chr12:41132508-41132509	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs373080773	chr12:41132512-41132513	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs548113304	chr12:41132622-41132623	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs565510629	chr12:41132674-41132675	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs12314733	chr12:41132728-41132729	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs550734649	chr12:41132797-41132798	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs569415738	chr12:41132810-41132811	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs536706449	chr12:41132853-41132854	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs548608493	chr12:41132861-41132862	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs370419120	chr12:41132871-41132872	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs559053465	chr12:41132898-41132899	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs534943971	chr12:41132934-41132935	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs1596540	chr12:41133023-41133024	Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs562169266	chr12:41133104-41133105	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs11836043	chr12:41133114-41133115	Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs140012726	chr12:41133127-41133128	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs145528316	chr12:41133133-41133134	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs575850563	chr12:41133176-41133177	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs147731098	chr12:41133204-41133205	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs113527600	chr12:41133205-41133206	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs559746860	chr12:41133234-41133235	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs540588150	chr12:41133347-41133348	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs77657502	chr12:41133365-41133366	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs532793209	chr12:41133366-41133367	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs186740667	chr12:41133389-41133390	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs192048182	chr12:41133408-41133409	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs182524757	chr12:41133451-41133452	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs548644729	chr12:41133456-41133457	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs139973869	chr12:41133488-41133489	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs528087421	chr12:41133494-41133495	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs187183126	chr12:41133576-41133577	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs56135334	chr12:41133577-41133578	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs542970382	chr12:41133587-41133588	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs546544915	chr12:41133632-41133633	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs571464300	chr12:41133639-41133640	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs149854885	chr12:41133681-41133682	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs557242695	chr12:41133696-41133697	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs569053077	chr12:41133699-41133700	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs536778931	chr12:41133712-41133713	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs555117985	chr12:41133750-41133751	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs573260699	chr12:41133755-41133756	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs561150470	chr12:41133772-41133773	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs73269741	chr12:41133865-41133866	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs143694066	chr12:41133960-41133961	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs376738415	chr12:41133962-41133963	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:62)

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
low-grade B-cell lymphoma tumor	18367492	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Glioma	20126413	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD

Chromatin state (count:608 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:41128400-41132600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
2	chr12:41128400-41141400	Weak transcription	Pancreatic Islets	Pancreatic Islet
3	chr12:41129800-41140600	Weak transcription	Ovary	ovary
4	chr12:41130000-41139200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
5	chr12:41131600-41135200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
6	chr12:41132600-41133200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
7	chr12:41133000-41133800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
8	chr12:41133000-41133800	Enhancers	NHEK	skin
9	chr12:41133400-41133600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
10	chr12:41133600-41145200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
11	chr12:41133800-41162400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
12	chr12:41139200-41139600	Enhancers	HUES6 Cell Line	embryonic stem cell
13	chr12:41139200-41140000	Enhancers	iPS-18 Cell Line	embryonic stem cell
14	chr12:41139400-41139600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
15	chr12:41139400-41139600	Enhancers	iPS-15b Cell Line	embryonic stem cell
16	chr12:41139400-41140600	Enhancers	HUES48 Cell Line	embryonic stem cell
17	chr12:41139600-41140000	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
18	chr12:41139600-41141400	Weak transcription	HUES6 Cell Line	embryonic stem cell
19	chr12:41139600-41141600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
20	chr12:41140000-41141600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
21	chr12:41140000-41143000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
22	chr12:41140400-41140600	Enhancers	Gastric	stomach
23	chr12:41140400-41141400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
24	chr12:41140600-41140800	Enhancers	Ovary	ovary
25	chr12:41140600-41141400	Weak transcription	HUES48 Cell Line	embryonic stem cell
26	chr12:41141200-41141400	Enhancers	A549	lung
27	chr12:41141400-41141600	Enhancers	Pancreatic Islets	Pancreatic Islet
28	chr12:41141400-41142000	Enhancers	HUES6 Cell Line	embryonic stem cell
29	chr12:41141400-41142400	Enhancers	HUES48 Cell Line	embryonic stem cell
30	chr12:41141400-41142400	Flanking Active TSS	A549	lung
31	chr12:41141400-41143600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
32	chr12:41141600-41142200	Enhancers	iPS-20b Cell Line	embryonic stem cell
33	chr12:41141600-41142200	Weak transcription	Pancreatic Islets	Pancreatic Islet
34	chr12:41141600-41142400	Enhancers	HUES64 Cell Line	embryonic stem cell
35	chr12:41141600-41142600	Enhancers	iPS-15b Cell Line	embryonic stem cell
36	chr12:41141600-41142600	Enhancers	iPS-18 Cell Line	embryonic stem cell
37	chr12:41141800-41142400	Enhancers	Brain Cingulate Gyrus	brain
38	chr12:41142000-41143600	Weak transcription	HUES6 Cell Line	embryonic stem cell
39	chr12:41142200-41142400	Enhancers	Pancreatic Islets	Pancreatic Islet
40	chr12:41142400-41143000	Enhancers	A549	lung
41	chr12:41142400-41145400	Weak transcription	HUES64 Cell Line	embryonic stem cell
42	chr12:41142400-41145600	Weak transcription	Brain Cingulate Gyrus	brain
43	chr12:41142600-41143600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
44	chr12:41143000-41143400	Weak transcription	A549	lung
45	chr12:41143000-41145400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
46	chr12:41143400-41144000	Enhancers	A549	lung
47	chr12:41143600-41144000	Enhancers	HUES6 Cell Line	embryonic stem cell
48	chr12:41143600-41144000	Enhancers	iPS-15b Cell Line	embryonic stem cell
49	chr12:41143600-41144000	Enhancers	Sigmoid Colon	Sigmoid Colon
50	chr12:41143600-41144200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived

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