Variant report

Variant	nsv899549
Chromosome Location	chr12:119385260-119431075
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	BACH1	chr12:119418338-119418558	H1-hESC	embryonic stem cell:	n/a	n/a
2	BACH1	chr12:119423914-119424114	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr12:119419234-119419779	H1-hESC	embryonic stem cell:	n/a	n/a
4	BHLHE40	chr12:119417687-119417852	GM12878	blood:	n/a	n/a
5	BRCA1	chr12:119418635-119418640	H1-hESC	embryonic stem cell:	n/a	n/a
6	CEBPB	chr12:119399124-119399442	K562	blood:	n/a	chr12:119399255-119399268 chr12:119399255-119399266
7	CEBPB	chr12:119392210-119392494	HepG2	liver:	n/a	chr12:119392333-119392344
8	CEBPB	chr12:119399103-119399445	HepG2	liver:	n/a	chr12:119399255-119399268 chr12:119399255-119399266
9	CEBPB	chr12:119400797-119401108	A549	lung:	n/a	chr12:119400972-119400983
10	CEBPB	chr12:119399113-119399430	A549	lung:	n/a	chr12:119399255-119399268 chr12:119399255-119399266
11	CEBPB	chr12:119400911-119401106	H1-hESC	embryonic stem cell:	n/a	chr12:119400972-119400983
12	CEBPB	chr12:119400818-119401128	K562	blood:	n/a	chr12:119400972-119400983
13	CEBPB	chr12:119400791-119401141	HepG2	liver:	n/a	chr12:119400972-119400983
14	CEBPB	chr12:119400799-119401160	IMR90	lung:	n/a	chr12:119400972-119400983
15	CHD1	chr12:119418298-119418447	H1-hESC	embryonic stem cell:	n/a	n/a
16	CHD2	chr12:119419032-119419832	H1-hESC	embryonic stem cell:	n/a	n/a
17	CHD2	chr12:119418587-119418685	H1-hESC	embryonic stem cell:	n/a	n/a
18	CREB1	chr12:119418918-119420181	H1-hESC	embryonic stem cell:	n/a	n/a
19	CREB1	chr12:119418927-119420130	H1-hESC	embryonic stem cell:	n/a	n/a
20	CTBP2	chr12:119418218-119419923	H1-hESC	embryonic stem cell:	n/a	n/a
21	CTCF	chr12:119417660-119417810	HepG2	liver:	n/a	chr12:119417751-119417772 chr12:119417749-119417767 chr12:119417750-119417766
22	CTCF	chr12:119417526-119417952	K562	blood:	n/a	chr12:119417751-119417772 chr12:119417749-119417767 chr12:119417750-119417766
23	CTCF	chr12:119417660-119417810	HPF	lung:	n/a	chr12:119417751-119417772 chr12:119417749-119417767 chr12:119417750-119417766
24	CTCF	chr12:119417437-119418017	MCF-7	breast:	n/a	chr12:119417751-119417772 chr12:119417749-119417767 chr12:119417750-119417766
25	CTCF	chr12:119417700-119417850	GM12864	blood:	n/a	chr12:119417751-119417772 chr12:119417749-119417767 chr12:119417750-119417766
26	CTCF	chr12:119419540-119419690	SK-N-SH_RA	brain:	n/a	n/a
27	CTCF	chr12:119417680-119417830	HEEpiC	esophagus:	n/a	chr12:119417751-119417772 chr12:119417749-119417767 chr12:119417750-119417766
28	CTCF	chr12:119417680-119417830	HRE	kidney:	n/a	chr12:119417751-119417772 chr12:119417749-119417767 chr12:119417750-119417766
29	CTCF	chr12:119417644-119417859	Kidney_OC	kidney:	n/a	chr12:119417751-119417772 chr12:119417749-119417767 chr12:119417750-119417766
30	CTCF	chr12:119417660-119417810	HBMEC	blood vessel:	n/a	chr12:119417751-119417772 chr12:119417749-119417767 chr12:119417750-119417766
31	CTCF	chr12:119387960-119388110	BE2_C	brain:	n/a	n/a
32	CTCF	chr12:119417700-119417850	HAc	cerebellar:	n/a	chr12:119417751-119417772 chr12:119417749-119417767 chr12:119417750-119417766
33	CTCF	chr12:119417660-119417810	SAEC	small airway:	n/a	chr12:119417751-119417772 chr12:119417749-119417767 chr12:119417750-119417766
34	CTCF	chr12:119417680-119417830	GM12869	blood:	n/a	chr12:119417751-119417772 chr12:119417749-119417767 chr12:119417750-119417766
35	CTCF	chr12:119417640-119417790	GM12878	blood:	n/a	chr12:119417751-119417772 chr12:119417749-119417767 chr12:119417750-119417766
36	CTCF	chr12:119417720-119417870	HCM	heart:	n/a	chr12:119417751-119417772 chr12:119417749-119417767 chr12:119417750-119417766
37	CTCF	chr12:119417600-119417750	HCM	heart:	n/a	n/a
38	CTCF	chr12:119417700-119417850	GM12873	blood:	n/a	chr12:119417751-119417772 chr12:119417749-119417767 chr12:119417750-119417766
39	CTCF	chr12:119417680-119417830	BE2_C	brain:	n/a	chr12:119417751-119417772 chr12:119417749-119417767 chr12:119417750-119417766
40	CTCF	chr12:119417632-119417887	NHEK	skin:	n/a	chr12:119417751-119417772 chr12:119417749-119417767 chr12:119417750-119417766
41	CTCF	chr12:119417651-119417875	Lung_OC	lung:	n/a	chr12:119417751-119417772 chr12:119417749-119417767 chr12:119417750-119417766
42	CTCF	chr12:119421820-119421970	BE2_C	brain:	n/a	n/a
43	CTCF	chr12:119417680-119417830	GM12878	blood:	n/a	chr12:119417751-119417772 chr12:119417749-119417767 chr12:119417750-119417766
44	CTCF	chr12:119417660-119417810	NB4	blood:	n/a	chr12:119417751-119417772 chr12:119417749-119417767 chr12:119417750-119417766
45	CTCF	chr12:119417660-119417810	HUVEC	blood vessel:	n/a	chr12:119417751-119417772 chr12:119417749-119417767 chr12:119417750-119417766
46	CTCF	chr12:119417580-119417730	WI-38	lung:	n/a	n/a
47	CTCF	chr12:119417644-119417869	HepG2	liver:	n/a	chr12:119417751-119417772 chr12:119417749-119417767 chr12:119417750-119417766
48	CTCF	chr12:119417700-119417850	GM12874	blood:	n/a	chr12:119417751-119417772 chr12:119417749-119417767 chr12:119417750-119417766
49	CTCF	chr12:119417605-119417866	SK-N-SH_RA	brain:	n/a	chr12:119417751-119417772 chr12:119417749-119417767 chr12:119417750-119417766
50	CTCF	chr12:119417660-119417810	NHDF-neo	bronchial:	n/a	chr12:119417751-119417772 chr12:119417749-119417767 chr12:119417750-119417766

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:119416585-119416635	Hela-S3	cervix:	n/a
2	chr12:119420927-119420977	HRE	kidney:	n/a
3	chr12:119416585-119416635	Hela-S3	cervix:	n/a
4	chr12:119420927-119420977	HRE	kidney:	n/a
5	chr12:119418622-119418672	HCF	heart:	n/a
6	chr12:119418676-119418726	AG09309	skin:	n/a
7	chr12:119419143-119419193	MCF10A-Er-Src	breast:	n/a
8	chr12:119419786-119419836	HRCEpiC	kidney:	n/a
9	chr12:119419786-119419836	BE2_C	brain:	n/a
10	chr12:119418676-119418726	HRE	kidney:	n/a
11	chr12:119419696-119419746	HepG2	liver:	n/a
12	chr12:119419786-119419836	BJ	skin:	n/a
13	chr12:119418004-119418054	NHBE	bronchial:	n/a
14	chr12:119418804-119418854	HCPEpiC	choroid plexus:	n/a
15	chr12:119416585-119416635	GM12892	blood:	n/a
16	chr12:119419331-119419381	GM12891	blood:	n/a
17	chr12:119423402-119423452	Jurkat	blood:	n/a
18	chr12:119418622-119418672	Jurkat	blood:	n/a
19	chr12:119418367-119418417	A549	lung:	n/a
20	chr12:119416585-119416635	PANC-1	pancreas:	n/a
21	chr12:119419696-119419746	HRCEpiC	kidney:	n/a
22	chr12:119419329-119419379	PANC-1	pancreas:	n/a
23	chr12:119420927-119420977	GM12878	blood:	n/a
24	chr12:119419331-119419381	HNPCEpiC	eye:	n/a
25	chr12:119418367-119418417	AG04449	skin:	fetal
26	chr12:119418004-119418054	ECC-1	luminal epithelium:	n/a
27	chr12:119420927-119420977	LNCaP	prostate:	n/a
28	chr12:119418367-119418417	U87	brain:	n/a
29	chr12:119419106-119419156	MCF10A-Er-Src	breast:	n/a
30	chr12:119418367-119418417	HCPEpiC	choroid plexus:	n/a
31	chr12:119420927-119420977	HMEC	breast:	n/a
32	chr12:119419143-119419193	HCPEpiC	choroid plexus:	n/a
33	chr12:119419696-119419746	BJ	skin:	n/a
34	chr12:119418804-119418854	HCF	heart:	n/a
35	chr12:119419106-119419156	HCT-116	colon:	n/a
36	chr12:119418804-119418854	Hepatocyte	liver:	n/a
37	chr12:119418004-119418054	NT2-D1	testis:	n/a
38	chr12:119417806-119417856	AG09319	gingival:	n/a
39	chr12:119420927-119420977	GM19239	blood:	n/a
40	chr12:119419106-119419156	Hepatocyte	liver:	n/a
41	chr12:119416585-119416635	ECC-1	luminal epithelium:	n/a
42	chr12:119418676-119418726	BE2_C	brain:	n/a
43	chr12:119419143-119419193	SK-N-SH_RA	brain:	n/a
44	chr12:119418622-119418672	PFSK-1	brain:	n/a
45	chr12:119419143-119419193	AG04450	lung:	fetal
46	chr12:119418367-119418417	SK-N-MC	brain:	n/a
47	chr12:119418622-119418672	PANC-1	pancreas:	n/a
48	chr12:119419331-119419381	GM06990	blood:	n/a
49	chr12:119419329-119419379	BJ	skin:	n/a
50	chr12:119417806-119417856	HIPEpiC	eye:	n/a

No.	Distal block	Cell Line	Cell type
1	chr12:119417235..119417851-chr12:119850790..119851632,2	K562	blood:
2	chr12:119417365..119417869-chr12:120086788..120087682,2	MCF-7	breast:
3	chr12:119411792..119414282-chr12:119618328..119620117,2	MCF-7	breast:
4	chr12:119418300..119419905-chr12:119423300..119425735,2	K562	blood:
5	chr12:119391457..119393836-chr12:119397133..119400298,3	K562	blood:
6	chr12:119391457..119394278-chr12:119398798..119400575,2	K562	blood:
7	chr12:119417707..119418245-chr12:119474754..119475351,2	MCF-7	breast:
8	chr12:119391322..119393259-chr12:119419157..119421683,2	MCF-7	breast:
9	chr12:119427403..119431135-chr12:119431729..119434900,3	K562	blood:
10	chr12:119391457..119393836-chr12:119397133..119400298,3	K562	blood:
11	chr12:119391457..119394278-chr12:119398798..119400575,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TAOK3-7	chr12:119392576-119392919	NONHSAT031060
2	lnc-TAOK3-7	chr12:119393794-119394018	NONHSAT031059
3	lnc-TAOK3-7	chr12:119392577-119392919	XLOC_010216
4	lnc-TAOK3-7	chr12:119393388-119393419	XLOC_010216
5	lnc-TAOK3-12	chr12:119386525-119387370	expReg_chr12_10652_-
6	lnc-TAOK3-13	chr12:119418009-119418111	ucscGeneNc_uc001tyk_1
7	lnc-TAOK3-13	chr12:119413206-119414296	ucscGeneNc_uc001tyk_1
8	lnc-TAOK3-7	chr12:119392576-119392919	NONHSAT031059
9	lnc-TAOK3-7	chr12:119393611-119393699	NONHSAT031059
10	lnc-TAOK3-7	chr12:119393388-119393428	NONHSAT031060

Variant related genes	Relation type
RN7SL508P	TF binding region
SRRM4	TF binding region
RN7SL508P	CpG island
SRRM4	CpG island
ENSG00000139767	chromatin interactions
MCL1	miRNA target sites
FSCN1	miRNA target sites

Extended variants
information (count: 967 )
Associated
traits (count: 72 )

Variant overlapped rSNPs/rCNVs (count:967 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs558353503	chr12:119386591-119386592	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
2	rs141542997	chr12:119386598-119386599	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
3	rs540669272	chr12:119386837-119386838	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
4	rs560503188	chr12:119386845-119386846	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
5	rs574106316	chr12:119386866-119386867	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
6	rs541110539	chr12:119386903-119386904	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
7	rs563269613	chr12:119386930-119386931	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
8	rs182856971	chr12:119386933-119386934	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
9	rs187538106	chr12:119386957-119386958	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
10	rs552387150	chr12:119386993-119386994	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
11	rs565230975	chr12:119386994-119386995	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
12	rs369700044	chr12:119387031-119387032	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
13	rs4492874	chr12:119387053-119387054	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
14	rs557824655	chr12:119387056-119387057	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
15	rs374192275	chr12:119387083-119387084	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
16	rs377705022	chr12:119387119-119387120	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
17	rs372468286	chr12:119387138-119387139	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
18	rs547583072	chr12:119387143-119387144	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
19	rs193160056	chr12:119387190-119387191	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
20	rs11069194	chr12:119387200-119387201	Inactive region	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs550474434	chr12:119387203-119387204	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
22	rs182814726	chr12:119387273-119387274	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
23	rs71451811	chr12:119387283-119387284	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
24	rs536679331	chr12:119387284-119387285	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
25	rs536335029	chr12:119387286-119387287	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
26	rs111227440	chr12:119387290-119387291	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
27	rs142917479	chr12:119387292-119387293	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
28	rs151078516	chr12:119387302-119387303	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
29	rs373649916	chr12:119387307-119387308	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
30	rs371160270	chr12:119387310-119387311	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
31	rs71069482	chr12:119387312-119387313	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
32	rs188330788	chr12:119387339-119387340	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
33	rs544128884	chr12:119387340-119387341	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
34	rs192227634	chr12:119387351-119387352	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
35	rs6490219	chr12:119391328-119391329	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs551269643	chr12:119391335-119391336	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs375534659	chr12:119391407-119391408	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs149397487	chr12:119391415-119391416	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs184004594	chr12:119391438-119391439	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs540910625	chr12:119391499-119391500	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs373123584	chr12:119391501-119391502	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs188000852	chr12:119391575-119391576	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs180912423	chr12:119391655-119391656	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs138427179	chr12:119391672-119391673	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs75132582	chr12:119391730-119391731	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs187086970	chr12:119391732-119391733	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs11069199	chr12:119391760-119391761	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs571556751	chr12:119391799-119391800	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs75539866	chr12:119391804-119391805	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs549014580	chr12:119391819-119391820	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:72)

Disease	PMID	Source
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
Chronic lymphocytic leukemia	21546498	CNVD
Medulloblastoma	21979893	CNVD
Malaria	21533027	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Basal cell lymphoma	17053054	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Autism	22495311	CNVD
T-cell prolymphocytic leukemia	19278963	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
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Glioblastoma multiforme	21390271	CNVD
Cancer	20164919	CNVD
Cancer	16751803	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Wilms tumour	21544195	CNVD
Ovarian cancer	21720365	CNVD
Colorectal cancer	16272173	CNVD
lymphocytic leukemia	21291569	CNVD
Breast cancer	16397240	CNVD
Sudden cardiac death	19188705	CNVD
Breast cancer	17133270	CNVD
Breast cancer	17603634	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Schizophrenia	18923514	CNVD
Schizophrenia	22241247	CNVD
Cryptorchidism	21048976	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Neuroblastoma	18923191	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Medulloblastoma	16783165	CNVD
Breast cancer	21509527	CNVD
Breast cancer	21806811	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Urothelial carcinoma	21177765	CNVD
Prostate cancer	18632612	CNVD
Myelofibrosis	22110671	CNVD
Beckwith-Wiedemann syndrome	20648245	CNVD
Developmental delay	21457577	CNVD
dysmorphic	21457577	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:238 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:119396000-119397200	Enhancers	iPS-18 Cell Line	embryonic stem cell
2	chr12:119396200-119396800	Enhancers	iPS-15b Cell Line	embryonic stem cell
3	chr12:119396200-119397000	Enhancers	ES-I3 Cell Line	embryonic stem cell
4	chr12:119396200-119397000	Enhancers	HUES6 Cell Line	embryonic stem cell
5	chr12:119396200-119397200	Enhancers	HUES48 Cell Line	embryonic stem cell
6	chr12:119396200-119397200	Enhancers	HUES64 Cell Line	embryonic stem cell
7	chr12:119396200-119397200	Enhancers	iPS-20b Cell Line	embryonic stem cell
8	chr12:119396400-119396600	Enhancers	Lung	lung
9	chr12:119396400-119396800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
10	chr12:119396600-119397000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
11	chr12:119397000-119397200	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell
12	chr12:119407800-119409600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
13	chr12:119408200-119409600	Enhancers	H9 Cell Line	embryonic stem cell
14	chr12:119408400-119409600	Enhancers	iPS-18 Cell Line	embryonic stem cell
15	chr12:119408600-119409400	Enhancers	HUES64 Cell Line	embryonic stem cell
16	chr12:119408600-119409600	Enhancers	iPS-15b Cell Line	embryonic stem cell
17	chr12:119408800-119409400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
18	chr12:119408800-119409400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
19	chr12:119409000-119410000	Bivalent Enhancer	Fetal Brain Male	brain
20	chr12:119414000-119417400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
21	chr12:119417400-119417600	Enhancers	H1 Cell Line	embryonic stem cell
22	chr12:119417400-119417600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
23	chr12:119417400-119417600	Enhancers	Fetal Brain Female	brain
24	chr12:119417400-119417800	Enhancers	HUES64 Cell Line	embryonic stem cell
25	chr12:119417400-119417800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
26	chr12:119417600-119417800	Enhancers	iPS-18 Cell Line	embryonic stem cell
27	chr12:119417600-119417800	Flanking Active TSS	Brain Germinal Matrix	brain
28	chr12:119417600-119418000	Flanking Active TSS	Fetal Brain Female	brain
29	chr12:119417600-119418000	Bivalent Enhancer	Skeletal Muscle Female	skeletal muscle
30	chr12:119417600-119418200	Enhancers	Fetal Brain Male	brain
31	chr12:119417600-119419800	Active TSS	H1 Cell Line	embryonic stem cell
32	chr12:119417600-119420200	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
33	chr12:119417800-119418000	Flanking Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
34	chr12:119417800-119418000	Enhancers	Placenta	Placenta
35	chr12:119417800-119418200	Active TSS	ES-I3 Cell Line	embryonic stem cell
36	chr12:119417800-119418200	Active TSS	HUES6 Cell Line	embryonic stem cell
37	chr12:119417800-119418200	Active TSS	Cortex derived primary cultured neurospheres	brain
38	chr12:119417800-119418200	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
39	chr12:119417800-119418400	Bivalent/Poised TSS	Brain Cingulate Gyrus	brain
40	chr12:119417800-119418400	Active TSS	Brain Germinal Matrix	brain
41	chr12:119417800-119418400	Bivalent/Poised TSS	Brain Hippocampus Middle	brain
42	chr12:119417800-119419000	Active TSS	Brain Anterior Caudate	brain
43	chr12:119417800-119419200	Bivalent Enhancer	Fetal Muscle Leg	muscle
44	chr12:119417800-119419600	Active TSS	ES-WA7 Cell Line	embryonic stem cell
45	chr12:119417800-119419600	Active TSS	HUES64 Cell Line	embryonic stem cell
46	chr12:119417800-119419600	Active TSS	iPS-20b Cell Line	embryonic stem cell
47	chr12:119417800-119419800	Active TSS	HUES48 Cell Line	embryonic stem cell
48	chr12:119417800-119419800	Active TSS	iPS-18 Cell Line	embryonic stem cell
49	chr12:119417800-119420000	Active TSS	H9 Cell Line	embryonic stem cell
50	chr12:119417800-119420000	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived

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