Variant report

Variant	nsv832454
Chromosome Location	chr12:72940798-73081180
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:449)
CpG islands
(count:244)
Chromatin interactive
region (count:6)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:449 , 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	chr12:72996821-72996840	K562	blood:	n/a	n/a
2	ATF1	chr12:73071729-73071865	K562	blood:	n/a	n/a
3	ATF1	chr12:72972257-72972407	K562	blood:	n/a	n/a
4	ATF2	chr12:73067526-73068137	GM12878	blood:	n/a	n/a
5	ATF2	chr12:73040903-73041319	GM12878	blood:	n/a	n/a
6	BACH1	chr12:73074983-73075111	H1-hESC	embryonic stem cell:	n/a	n/a
7	BATF	chr12:73040940-73041214	GM12878	blood:	n/a	n/a
8	BCLAF1	chr12:73067501-73068061	GM12878	blood:	n/a	n/a
9	BHLHE40	chr12:73067799-73068001	GM12878	blood:	n/a	n/a
10	BHLHE40	chr12:73066581-73066626	GM12878	blood:	n/a	n/a
11	BHLHE40	chr12:73069299-73069320	GM12878	blood:	n/a	n/a
12	BRCA1	chr12:73036607-73036730	Hela-S3	cervix:	n/a	n/a
13	CEBPB	chr12:73074666-73074866	A549	lung:	n/a	chr12:73074782-73074795 chr12:73074779-73074796
14	CEBPB	chr12:72964395-72964834	MCF-7	breast:	n/a	chr12:72964771-72964782 chr12:72964707-72964720 chr12:72964709-72964720
15	CEBPB	chr12:72977738-72977827	K562	blood:	n/a	n/a
16	CEBPB	chr12:72972166-72972437	K562	blood:	n/a	chr12:72972341-72972354
17	CEBPB	chr12:72941360-72941768	IMR90	lung:	n/a	n/a
18	CEBPB	chr12:72945788-72945988	HepG2	liver:	n/a	chr12:72945852-72945863
19	CEBPB	chr12:73020979-73021186	HepG2	liver:	n/a	chr12:73021076-73021087
20	CEBPB	chr12:72972164-72972518	K562	blood:	n/a	chr12:72972341-72972354
21	CEBPB	chr12:73026095-73026405	IMR90	lung:	n/a	chr12:73026256-73026269
22	CEBPB	chr12:73063480-73063680	HepG2	liver:	n/a	chr12:73063547-73063560 chr12:73063601-73063618
23	CEBPB	chr12:73058184-73058384	H1-hESC	embryonic stem cell:	n/a	n/a
24	CEBPB	chr12:72964447-72964799	H1-hESC	embryonic stem cell:	n/a	chr12:72964771-72964782 chr12:72964707-72964720 chr12:72964709-72964720
25	CEBPB	chr12:73017088-73017288	HepG2	liver:	n/a	chr12:73017175-73017186
26	CEBPB	chr12:73005979-73006406	H1-hESC	embryonic stem cell:	n/a	n/a
27	CHD2	chr12:73067777-73067994	GM12878	blood:	n/a	n/a
28	CTCF	chr12:72964520-72964670	BJ	skin:	n/a	n/a
29	CTCF	chr12:72964500-72964650	GM12801	blood:	n/a	n/a
30	CTCF	chr12:72964453-72964738	H1-hESC	embryonic stem cell:	n/a	n/a
31	CTCF	chr12:72950840-72950990	MCF-7	breast:	n/a	n/a
32	CTCF	chr12:73004941-73004984	Kidney_OC	kidney:	n/a	n/a
33	CTCF	chr12:72964480-72964630	GM12874	blood:	n/a	n/a
34	CTCF	chr12:72964500-72964650	HepG2	liver:	n/a	n/a
35	CTCF	chr12:72964420-72964570	HAc	cerebellar:	n/a	n/a
36	CTCF	chr12:72954220-72954370	GM12873	blood:	n/a	n/a
37	CTCF	chr12:72964520-72964670	HPAF	blood vessel:	n/a	n/a
38	CTCF	chr12:73031470-73031506	Spleen_OC	spleen:	n/a	n/a
39	CTCF	chr12:72964359-72964684	H1-hESC	embryonic stem cell:	n/a	n/a
40	CTCF	chr12:72954280-72954430	HRPEpiC	eye:	n/a	n/a
41	CTCF	chr12:72964497-72964609	GM10248	blood:	n/a	n/a
42	CTCF	chr12:72964480-72964630	GM12871	blood:	n/a	n/a
43	CTCF	chr12:72964491-72964701	MCF-7	breast:	n/a	n/a
44	CTCF	chr12:72964468-72964677	Medullo	brain:	n/a	n/a
45	CTCF	chr12:72964501-72964689	H1-hESC	embryonic stem cell:	n/a	n/a
46	CTCF	chr12:72964500-72964650	GM06990	blood:	n/a	n/a
47	CTCF	chr12:72954140-72954290	HRPEpiC	eye:	n/a	n/a
48	CTCF	chr12:72964449-72964874	MCF-7	breast:	n/a	n/a
49	CTCF	chr12:72964380-72964530	A549	lung:	n/a	n/a
50	CTCF	chr12:72954260-72954410	HBMEC	blood vessel:	n/a	n/a

(count:244 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:72941283-72941333	SAEC	small airway:	n/a
2	chr12:73034008-73034058	HMEC	breast:	n/a
3	chr12:73057369-73057419	SAEC	small airway:	n/a
4	chr12:73057369-73057419	HEEpiC	esophagus:	n/a
5	chr12:72941283-72941333	HepG2	liver:	n/a
6	chr12:73005050-73005100	Hela-S3	cervix:	n/a
7	chr12:73057369-73057419	NB4	blood:	n/a
8	chr12:73057369-73057419	HRE	kidney:	n/a
9	chr12:73057369-73057419	Hela-S3	cervix:	n/a
10	chr12:72941283-72941333	PrEC	prostate:	n/a
11	chr12:73057369-73057419	NT2-D1	testis:	n/a
12	chr12:73005050-73005100	AoSMC	blood vessel:	n/a
13	chr12:73057369-73057419	A549	lung:	n/a
14	chr12:73057369-73057419	CMK	blood:	n/a
15	chr12:73034008-73034058	PrEC	prostate:	n/a
16	chr12:73005050-73005100	LNCaP	prostate:	n/a
17	chr12:73057369-73057419	Caco-2	colon:	n/a
18	chr12:73057369-73057419	K562	blood:	n/a
19	chr12:73034008-73034058	HRPEpiC	eye:	n/a
20	chr12:72941283-72941333	NHBE	bronchial:	n/a
21	chr12:73005050-73005100	NHBE	bronchial:	n/a
22	chr12:73005050-73005100	H1-hESC	embryonic stem cell:	embryo
23	chr12:72941283-72941333	T-47D	breast:	n/a
24	chr12:73034008-73034058	HEK293	kidney:	embryo
25	chr12:73005050-73005100	A549	lung:	n/a
26	chr12:73057369-73057419	HL-60	blood:	n/a
27	chr12:73057369-73057419	Hepatocyte	liver:	n/a
28	chr12:73005050-73005100	HL-60	blood:	n/a
29	chr12:73057369-73057419	GM06990	blood:	n/a
30	chr12:72941283-72941333	HRE	kidney:	n/a
31	chr12:72941283-72941333	BE2_C	brain:	n/a
32	chr12:73057369-73057419	HMEC	breast:	n/a
33	chr12:73057369-73057419	SK-N-SH_RA	brain:	n/a
34	chr12:73057369-73057419	NHDF-neo	bronchial:	n/a
35	chr12:72941283-72941333	RPTEC	kidney:	n/a
36	chr12:72941283-72941333	HUVEC	blood vessel:	n/a
37	chr12:73057369-73057419	Jurkat	blood:	n/a
38	chr12:73034008-73034058	IMR90	lung:	fetal
39	chr12:72941283-72941333	HEK293	kidney:	embryo
40	chr12:73057369-73057419	HepG2	liver:	n/a
41	chr12:72941283-72941333	NHDF-neo	bronchial:	n/a
42	chr12:73057369-73057419	HCM	heart:	n/a
43	chr12:73005050-73005100	AG09309	skin:	n/a
44	chr12:73057369-73057419	HUVEC	blood vessel:	n/a
45	chr12:73057369-73057419	HCF	heart:	n/a
46	chr12:73057369-73057419	ProgFib	skin:	n/a
47	chr12:72941283-72941333	MCF10A-Er-Src	breast:	n/a
48	chr12:72941283-72941333	GM12878	blood:	n/a
49	chr12:73057369-73057419	PANC-1	pancreas:	n/a
50	chr12:73057369-73057419	BJ	skin:	n/a

(count:6 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:72945974..72947859-chr12:72949789..72952679,2	MCF-7	breast:
2	chr12:73050089..73050693-chr4:90478139..90478639,2	MCF-7	breast:
3	chr12:73066407..73068991-chr12:73070185..73072919,2	K562	blood:
4	chr12:73066407..73068991-chr12:73070185..73072919,2	K562	blood:
5	chr12:72945974..72947859-chr12:72949789..72952679,2	MCF-7	breast:
6	chr12:73003659..73006224-chr12:73008245..73010751,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TPH2-5	chr12:73004458-73005096	NONHSAT029473
2	lnc-ZFC3H1-14	chr12:73061098-73061371	NONHSAT029474
3	lnc-ZFC3H1-15	chr12:73065223-73065430	NONHSAT029475

No data

Variant related genes	Relation type
CHCHD3P2	TF binding region
TRHDE	TF binding region
CHCHD3P2	CpG island
TRHDE	CpG island
ENSG00000257723	chromatin interactions

Extended variants
information (count: 4248 )
Associated
traits (count: 73 )

Variant overlapped rSNPs/rCNVs (count:4248 , 50 per page) page: 1 2 3 4 5 6 7 ... 85

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs541989587	chr12:72940808-72940809	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs1214898	chr12:72940822-72940823	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs562887223	chr12:72940830-72940831	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs539410790	chr12:72940848-72940849	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs574755470	chr12:72940914-72940915	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs573284434	chr12:72940932-72940933	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs542278835	chr12:72940935-72940936	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs575677605	chr12:72941006-72941007	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs150110275	chr12:72941008-72941009	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs527608138	chr12:72941013-72941014	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs193030420	chr12:72941021-72941022	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs182987043	chr12:72941048-72941049	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs544640698	chr12:72941054-72941055	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs116739075	chr12:72941139-72941140	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs549824245	chr12:72941146-72941147	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs187527826	chr12:72941235-72941236	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs535393361	chr12:72941302-72941303	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs564724025	chr12:72941315-72941316	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs193000009	chr12:72941367-72941368	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs138424672	chr12:72941398-72941399	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs184698324	chr12:72941404-72941405	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs571020045	chr12:72941470-72941471	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs11179244	chr12:72941510-72941511	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs538085148	chr12:72941531-72941532	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs188379497	chr12:72941544-72941545	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs533677258	chr12:72941559-72941560	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs192116461	chr12:72941560-72941561	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs149277929	chr12:72941572-72941573	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs554215529	chr12:72941613-72941614	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs184244484	chr12:72941639-72941640	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs528967662	chr12:72941656-72941657	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs74103382	chr12:72941724-72941725	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs548769357	chr12:72941811-72941812	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs568954177	chr12:72941827-72941828	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs564271887	chr12:72941840-72941841	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs146108676	chr12:72941841-72941842	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs543265981	chr12:72941965-72941966	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs561791849	chr12:72941970-72941971	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs536993278	chr12:72942001-72942002	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs559089011	chr12:72942002-72942003	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs528956411	chr12:72942050-72942051	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs546947935	chr12:72942071-72942072	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs565327333	chr12:72942122-72942123	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs189397258	chr12:72942133-72942134	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs182045752	chr12:72942151-72942152	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs372928271	chr12:72942191-72942192	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs531160588	chr12:72942211-72942212	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs184595193	chr12:72942258-72942259	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs556502558	chr12:72942290-72942291	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs568494776	chr12:72942322-72942323	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:73)

Disease	PMID	Source
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
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
Neurodevelopmental disorder	22521361	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
Breast cancer	17899364	CNVD
Colorectal cancer	16272173	CNVD
Cancer	16751803	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
small cell lung cancer	20016488	CNVD
Melanoma	18172304	CNVD
Glioblastoma multiforme	21390271	CNVD
Cancer	20164919	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	21785460	CNVD
Acute myeloid leukemia	21251322	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Burkitt''s lymphoma	20823134	CNVD
abnormal development	18461090	CNVD
Prostate cancer	18632612	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Breast cancer	16620391	CNVD
Disease	21505450	CNVD
craniofacial dysmorphism	21918468	CNVD
Breast cancer	21364760	CNVD
Breast cancer	17133270	CNVD
Autism	20685689	CNVD
Urothelial cell carcinoma	18451213	CNVD
Myelofibrosis	22110671	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Breast cancer	22032731	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
Hodgkin''s lymphoma	18641027	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Cancer	20164920	CNVD
Acute myeloid leukemia	20729466	CNVD

Chromatin state (count:223 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:72935000-72941000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr12:72939600-72941600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
3	chr12:72940000-72940800	Enhancers	Adipose Nuclei	Adipose
4	chr12:72940200-72940800	Enhancers	Fetal Heart	heart
5	chr12:72940400-72941600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
6	chr12:72940400-72942000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
7	chr12:72940600-72940800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
8	chr12:72940600-72941600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
9	chr12:72940600-72941800	Enhancers	HUES48 Cell Line	embryonic stem cell
10	chr12:72940600-72942000	Enhancers	iPS-15b Cell Line	embryonic stem cell
11	chr12:72940600-72942600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
12	chr12:72940800-72941400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
13	chr12:72940800-72941600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
14	chr12:72941000-72942000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
15	chr12:72941200-72941600	Enhancers	iPS-18 Cell Line	embryonic stem cell
16	chr12:72941400-72941600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
17	chr12:72941400-72941800	Enhancers	iPS-20b Cell Line	embryonic stem cell
18	chr12:72941400-72942000	Enhancers	HUES64 Cell Line	embryonic stem cell
19	chr12:72941600-72942600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
20	chr12:72941600-72959800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
21	chr12:72942000-72948400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
22	chr12:72942600-72943000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
23	chr12:72942800-72943000	Enhancers	iPS-18 Cell Line	embryonic stem cell
24	chr12:72947600-72973600	Weak transcription	Fetal Intestine Small	intestine
25	chr12:72948400-72948600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
26	chr12:72953600-72954200	Enhancers	Fetal Heart	heart
27	chr12:72956400-72959400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
28	chr12:72956400-72973800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
29	chr12:72957600-72958000	Weak transcription	Pancreas	Pancrea
30	chr12:72957800-72958000	Bivalent Enhancer	Breast Myoepithelial Primary Cells	Breast
31	chr12:72958000-72958200	ZNF genes & repeats	Pancreas	Pancrea
32	chr12:72958200-72984400	Weak transcription	Pancreas	Pancrea
33	chr12:72964400-72986800	Weak transcription	Fetal Intestine Large	intestine
34	chr12:72964600-72965200	Enhancers	iPS-18 Cell Line	embryonic stem cell
35	chr12:72964800-72965400	Enhancers	iPS-20b Cell Line	embryonic stem cell
36	chr12:72965000-72965800	Enhancers	HUES48 Cell Line	embryonic stem cell
37	chr12:72970600-72982800	Weak transcription	Ovary	ovary
38	chr12:72971200-72978600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
39	chr12:72977400-72978000	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
40	chr12:72978600-72978800	Genic enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
41	chr12:72978600-72978800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
42	chr12:72978800-72982000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
43	chr12:72979200-72980800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
44	chr12:72979200-72981000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
45	chr12:72979200-72981200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
46	chr12:72979800-72980800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
47	chr12:72980000-72980400	Enhancers	HUES64 Cell Line	embryonic stem cell
48	chr12:72980000-72980600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
49	chr12:72980000-72980600	Enhancers	HUES6 Cell Line	embryonic stem cell
50	chr12:72980200-72980600	Enhancers	iPS-18 Cell Line	embryonic stem cell

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