Variant report

Variant	nsv899552
Chromosome Location	chr12:119733874-119814623
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:444)
CpG islands
(count:915)
Chromatin interactive
region (count:11)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:444 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr12:119803212-119803732	HepG2	liver:	n/a	n/a
2	ATF1	chr12:119778457-119778752	K562	blood:	n/a	n/a
3	ATF3	chr12:119741129-119741350	K562	blood:	n/a	n/a
4	ATF3	chr12:119741124-119741413	H1-hESC	embryonic stem cell:	n/a	n/a
5	ATF3	chr12:119778421-119778778	K562	blood:	n/a	chr12:119778607-119778618 chr12:119778607-119778620 chr12:119778608-119778619 chr12:119778606-119778616 chr12:119778606-119778619 chr12:119778609-119778619 chr12:119778606-119778619 chr12:119778609-119778619 chr12:119778609-119778616 chr12:119778608-119778616 chr12:119778605-119778620 chr12:119778607-119778618 chr12:119778605-119778618
6	ATF3	chr12:119741184-119741308	GM12878	blood:	n/a	n/a
7	BACH1	chr12:119765991-119766222	H1-hESC	embryonic stem cell:	n/a	n/a
8	BATF	chr12:119813500-119813772	GM12878	blood:	n/a	chr12:119813647-119813658
9	BATF	chr12:119813452-119813791	GM12878	blood:	n/a	chr12:119813647-119813658
10	BCL11A	chr12:119776785-119777103	H1-hESC	embryonic stem cell:	n/a	n/a
11	BHLHE40	chr12:119741114-119741379	K562	blood:	n/a	n/a
12	BHLHE40	chr12:119757656-119757836	K562	blood:	n/a	n/a
13	BRCA1	chr12:119772882-119772889	GM12878	blood:	n/a	n/a
14	CEBPB	chr12:119810432-119810654	A549	lung:	n/a	chr12:119810539-119810552 chr12:119810539-119810550
15	CEBPB	chr12:119739407-119739537	HepG2	liver:	n/a	n/a
16	CEBPB	chr12:119739316-119739526	Hela-S3	cervix:	n/a	n/a
17	CEBPB	chr12:119794415-119794663	K562	blood:	n/a	n/a
18	CEBPB	chr12:119794425-119794742	Hela-S3	cervix:	n/a	n/a
19	CEBPB	chr12:119739274-119739559	A549	lung:	n/a	n/a
20	CEBPB	chr12:119810370-119810723	HepG2	liver:	n/a	chr12:119810539-119810552 chr12:119810539-119810550
21	CEBPB	chr12:119739252-119739625	MCF-7	breast:	n/a	n/a
22	CEBPB	chr12:119803466-119803681	HepG2	liver:	n/a	n/a
23	CEBPB	chr12:119739293-119739581	K562	blood:	n/a	n/a
24	CEBPB	chr12:119736371-119736694	Hela-S3	cervix:	n/a	n/a
25	CEBPB	chr12:119736449-119736550	A549	lung:	n/a	n/a
26	CHD2	chr12:119772289-119772588	K562	blood:	n/a	n/a
27	CHD2	chr12:119741125-119741297	H1-hESC	embryonic stem cell:	n/a	n/a
28	CHD2	chr12:119772278-119772627	H1-hESC	embryonic stem cell:	n/a	n/a
29	CREB1	chr12:119766001-119766213	H1-hESC	embryonic stem cell:	n/a	n/a
30	CTCF	chr12:119739366-119739527	GM12878	blood:	n/a	n/a
31	CTCF	chr12:119766060-119766210	GM12865	blood:	n/a	n/a
32	CTCF	chr12:119766024-119766213	GM12891	blood:	n/a	n/a
33	CTCF	chr12:119779580-119779730	GM12864	blood:	n/a	n/a
34	CTCF	chr12:119740780-119740930	BE2_C	brain:	n/a	n/a
35	CTCF	chr12:119766040-119766262	SK-N-SH_RA	brain:	n/a	n/a
36	CTCF	chr12:119766004-119766257	GM12878	blood:	n/a	n/a
37	CTCF	chr12:119766010-119766248	GM12892	blood:	n/a	n/a
38	CTCF	chr12:119779620-119779730	Medullo	brain:	n/a	n/a
39	CTCF	chr12:119739337-119739429	MCF-7	breast:	n/a	n/a
40	CTCF	chr12:119779600-119779750	WERI-Rb-1	eye:	n/a	n/a
41	CTCF	chr12:119766060-119766210	GM12869	blood:	n/a	n/a
42	CTCF	chr12:119766020-119766170	GM12864	blood:	n/a	n/a
43	CTCF	chr12:119766040-119766190	MCF-7	breast:	n/a	n/a
44	CTCF	chr12:119782100-119782250	GM12871	blood:	n/a	n/a
45	CTCF	chr12:119766002-119766241	MCF-7	breast:	n/a	n/a
46	CTCF	chr12:119765984-119766264	Medullo	brain:	n/a	n/a
47	CTCF	chr12:119766080-119766230	A549	lung:	n/a	n/a
48	CTCF	chr12:119757552-119757579	LNCaP	prostate:	n/a	n/a
49	CTCF	chr12:119739360-119739510	GM12875	blood:	n/a	n/a
50	CTCF	chr12:119766040-119766190	GM12871	blood:	n/a	n/a

(count:915 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:119741507-119741557	HEEpiC	esophagus:	n/a
2	chr12:119772354-119772404	U87	brain:	n/a
3	chr12:119771596-119771646	HCT-116	colon:	n/a
4	chr12:119742417-119742467	Jurkat	blood:	n/a
5	chr12:119772577-119772627	ovcar-3	ovarian:	n/a
6	chr12:119772577-119772627	RPTEC	kidney:	n/a
7	chr12:119771257-119771307	AG04449	skin:	fetal
8	chr12:119772381-119772431	HUVEC	blood vessel:	n/a
9	chr12:119772421-119772471	HUVEC	blood vessel:	n/a
10	chr12:119769357-119769407	SKMC	muscle:	n/a
11	chr12:119772421-119772471	PFSK-1	brain:	n/a
12	chr12:119740840-119740890	AG04449	skin:	fetal
13	chr12:119798505-119798555	A549	lung:	n/a
14	chr12:119798505-119798555	HAEpiC	amniotic membrane:	n/a
15	chr12:119742417-119742467	NB4	blood:	n/a
16	chr12:119776178-119776228	GM19239	blood:	n/a
17	chr12:119741507-119741557	ProgFib	skin:	n/a
18	chr12:119772577-119772627	AG09309	skin:	n/a
19	chr12:119740840-119740890	NT2-D1	testis:	n/a
20	chr12:119772421-119772471	MCF-7	breast:	n/a
21	chr12:119769357-119769407	RPTEC	kidney:	n/a
22	chr12:119771596-119771646	HRPEpiC	eye:	n/a
23	chr12:119772364-119772414	T-47D	breast:	n/a
24	chr12:119772364-119772414	SAEC	small airway:	n/a
25	chr12:119772381-119772431	H1-hESC	embryonic stem cell:	embryo
26	chr12:119772364-119772414	HEK293	kidney:	embryo
27	chr12:119742417-119742467	NHBE	bronchial:	n/a
28	chr12:119776178-119776228	Caco-2	colon:	n/a
29	chr12:119772381-119772431	LNCaP	prostate:	n/a
30	chr12:119772421-119772471	ovcar-3	ovarian:	n/a
31	chr12:119772364-119772414	LNCaP	prostate:	n/a
32	chr12:119741254-119741304	SAEC	small airway:	n/a
33	chr12:119769357-119769407	HepG2	liver:	n/a
34	chr12:119771596-119771646	HAEpiC	amniotic membrane:	n/a
35	chr12:119776178-119776228	HEK293	kidney:	embryo
36	chr12:119771596-119771646	Caco-2	colon:	n/a
37	chr12:119776178-119776228	ECC-1	luminal epithelium:	n/a
38	chr12:119772354-119772404	HEK293	kidney:	embryo
39	chr12:119742417-119742467	PrEC	prostate:	n/a
40	chr12:119741254-119741304	NT2-D1	testis:	n/a
41	chr12:119772421-119772471	PANC-1	pancreas:	n/a
42	chr12:119742417-119742467	HEK293	kidney:	embryo
43	chr12:119772421-119772471	GM12892	blood:	n/a
44	chr12:119798505-119798555	GM19239	blood:	n/a
45	chr12:119772364-119772414	HCT-116	colon:	n/a
46	chr12:119772421-119772471	Caco-2	colon:	n/a
47	chr12:119772354-119772404	RPTEC	kidney:	n/a
48	chr12:119771596-119771646	NHBE	bronchial:	n/a
49	chr12:119772577-119772627	HL-60	blood:	n/a
50	chr12:119772364-119772414	HNPCEpiC	eye:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr12:119774496..119776327-chr12:119777022..119779114,2	K562	blood:
2	chr12:119806583..119808984-chr12:119813219..119815539,2	K562	blood:
3	chr12:119739534..119741521-chr12:119743131..119745914,2	MCF-7	breast:
4	chr12:119777510..119778281-chr3:182539096..182539983,2	MCF-7	breast:
5	chr12:119765655..119766458-chr12:119850699..119851560,2	MCF-7	breast:
6	chr12:119774496..119776327-chr12:119777022..119779114,2	K562	blood:
7	chr12:119764864..119767176-chr12:119782140..119784942,2	MCF-7	breast:
8	chr12:119806583..119808984-chr12:119813219..119815539,2	K562	blood:
9	chr12:119765671..119766355-chr12:119850911..119851698,3	K562	blood:
10	chr12:119739534..119741521-chr12:119743131..119745914,2	MCF-7	breast:
11	chr12:119764864..119767176-chr12:119782140..119784942,2	MCF-7	breast:

(count:3 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CIT-2	chr12:119741140-119741185	XLOC_010217
2	lnc-CIT-2	chr12:119739414-119739836	XLOC_010217
3	lnc-HSPB8-7	chr12:119773016-119773071	NONHSAT031079

No data

Variant related genes	Relation type
CCDC60	TF binding region
CCDC60	CpG island

Extended variants
information (count: 2344 )
Associated
traits (count: 73 )

Variant overlapped rSNPs/rCNVs (count:2344 , 50 per page) page: 1 2 3 4 5 6 7 ... 47

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2727733	chr12:119733874-119733875	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs372501396	chr12:119733906-119733907	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs568704835	chr12:119733907-119733908	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs537188036	chr12:119733939-119733940	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs370322621	chr12:119733954-119733955	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs532560056	chr12:119733961-119733962	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs182269288	chr12:119733976-119733977	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs534736373	chr12:119733980-119733981	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs148867144	chr12:119733983-119733984	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs186810662	chr12:119733984-119733985	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs7305439	chr12:119733999-119734000	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs146992273	chr12:119734012-119734013	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs558568641	chr12:119734033-119734034	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs190084578	chr12:119734045-119734046	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs181292915	chr12:119734070-119734071	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs116149759	chr12:119734094-119734095	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs185658689	chr12:119734117-119734118	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs79265436	chr12:119734193-119734194	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs147583576	chr12:119734216-119734217	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs539865512	chr12:119734217-119734218	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs556739321	chr12:119734247-119734248	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs560069734	chr12:119734260-119734261	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs529193797	chr12:119734287-119734288	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs548853998	chr12:119734313-119734314	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs61939513	chr12:119734380-119734381	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs142116759	chr12:119734381-119734382	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs562400768	chr12:119734386-119734387	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs115299916	chr12:119734391-119734392	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs76493621	chr12:119734396-119734397	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs531404386	chr12:119734406-119734407	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs551523904	chr12:119734448-119734449	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs570872203	chr12:119734453-119734454	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs539906112	chr12:119734470-119734471	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs2555301	chr12:119734472-119734473	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs543729539	chr12:119734498-119734499	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs143872151	chr12:119734534-119734535	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs145761313	chr12:119734548-119734549	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs556106387	chr12:119734549-119734550	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs374180196	chr12:119734559-119734560	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs538079122	chr12:119734694-119734695	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs117538163	chr12:119734698-119734699	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs190071336	chr12:119734706-119734707	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs56754520	chr12:119734753-119734754	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs553389057	chr12:119734769-119734770	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs148183647	chr12:119734799-119734800	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs11608825	chr12:119734895-119734896	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs545275752	chr12:119734899-119734900	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs562464154	chr12:119734924-119734925	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs531466972	chr12:119734961-119734962	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs2555300	chr12:119734962-119734963	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance

Variant related diseases (count:73)

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
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:356 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:119729800-119746600	Weak transcription	Right Atrium	heart
2	chr12:119732800-119734400	Weak transcription	Fetal Lung	lung
3	chr12:119733400-119736400	Enhancers	Fetal Heart	heart
4	chr12:119733400-119739000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
5	chr12:119734200-119734400	Enhancers	Spleen	Spleen
6	chr12:119734400-119734800	Enhancers	Fetal Lung	lung
7	chr12:119736000-119736800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
8	chr12:119736400-119736600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
9	chr12:119737000-119740000	Weak transcription	Lung	lung
10	chr12:119738800-119739000	Enhancers	iPS-20b Cell Line	embryonic stem cell
11	chr12:119738800-119739000	Bivalent Enhancer	Fetal Brain Female	brain
12	chr12:119739000-119740200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
13	chr12:119739000-119741800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
14	chr12:119739200-119739400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
15	chr12:119739400-119740800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
16	chr12:119740000-119741200	Enhancers	Brain Germinal Matrix	brain
17	chr12:119740200-119740400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
18	chr12:119740200-119740400	Enhancers	Fetal Stomach	stomach
19	chr12:119740200-119740400	Enhancers	Lung	lung
20	chr12:119740200-119740600	Enhancers	HUES6 Cell Line	embryonic stem cell
21	chr12:119740200-119740600	Enhancers	iPS-20b Cell Line	embryonic stem cell
22	chr12:119740200-119740600	Enhancers	Brain Cingulate Gyrus	brain
23	chr12:119740200-119740600	Enhancers	Brain Substantia Nigra	brain
24	chr12:119740200-119740800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
25	chr12:119740200-119741000	Enhancers	Fetal Muscle Leg	muscle
26	chr12:119740200-119741200	Enhancers	HUES64 Cell Line	embryonic stem cell
27	chr12:119740200-119741200	Enhancers	iPS-18 Cell Line	embryonic stem cell
28	chr12:119740200-119741200	Enhancers	Brain Anterior Caudate	brain
29	chr12:119740200-119741200	Enhancers	Brain Hippocampus Middle	brain
30	chr12:119740200-119741200	Enhancers	Brain Inferior Temporal Lobe	brain
31	chr12:119740400-119740600	Enhancers	Fetal Muscle Trunk	muscle
32	chr12:119740400-119741000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
33	chr12:119740400-119741200	Enhancers	ES-I3 Cell Line	embryonic stem cell
34	chr12:119740600-119741000	Enhancers	Cortex derived primary cultured neurospheres	brain
35	chr12:119740800-119741400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
36	chr12:119741000-119741200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
37	chr12:119741200-119746600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
38	chr12:119741200-119746600	Weak transcription	Brain Hippocampus Middle	brain
39	chr12:119741400-119741600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
40	chr12:119741800-119745600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
41	chr12:119744200-119744600	Enhancers	Esophagus	oesophagus
42	chr12:119744400-119744600	Enhancers	HUES48 Cell Line	embryonic stem cell
43	chr12:119744400-119744600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
44	chr12:119744400-119744600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
45	chr12:119744600-119746600	Weak transcription	Esophagus	oesophagus
46	chr12:119744600-119746800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
47	chr12:119744800-119746600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
48	chr12:119745600-119745800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
49	chr12:119745800-119746000	Bivalent Enhancer	Fetal Muscle Leg	muscle
50	chr12:119745800-119746200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived

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