Variant report

Variant	nsv899132
Chromosome Location	chr12:60087572-60211476
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	ARID3A	chr12:60117978-60118448	HepG2	liver:	n/a	n/a
2	BATF	chr12:60174486-60174690	GM12878	blood:	n/a	n/a
3	CEBPB	chr12:60190587-60190853	MCF-7	breast:	n/a	chr12:60190769-60190780
4	CEBPB	chr12:60137739-60137957	IMR90	lung:	n/a	n/a
5	CEBPB	chr12:60089199-60089549	IMR90	lung:	n/a	n/a
6	CEBPB	chr12:60103775-60104229	HepG2	liver:	n/a	chr12:60104182-60104193
7	CEBPB	chr12:60093432-60093776	MCF-7	breast:	n/a	chr12:60093595-60093606
8	CEBPB	chr12:60202229-60202494	MCF-7	breast:	n/a	n/a
9	CEBPB	chr12:60092223-60092841	IMR90	lung:	n/a	n/a
10	CEBPB	chr12:60092476-60092745	HepG2	liver:	n/a	n/a
11	CEBPB	chr12:60092384-60092795	A549	lung:	n/a	n/a
12	CEBPB	chr12:60093373-60093796	Hela-S3	cervix:	n/a	chr12:60093595-60093606
13	CEBPB	chr12:60093364-60093972	IMR90	lung:	n/a	chr12:60093595-60093606
14	CEBPB	chr12:60117309-60117679	IMR90	lung:	n/a	chr12:60117487-60117496 chr12:60117487-60117496 chr12:60117485-60117498 chr12:60117579-60117590 chr12:60117487-60117498 chr12:60117487-60117496 chr12:60117485-60117496 chr12:60117487-60117496
15	CEBPB	chr12:60117375-60117579	HepG2	liver:	n/a	chr12:60117487-60117496 chr12:60117487-60117496 chr12:60117485-60117498 chr12:60117487-60117498 chr12:60117487-60117496 chr12:60117485-60117496 chr12:60117487-60117496
16	CEBPB	chr12:60117357-60117581	MCF-7	breast:	n/a	chr12:60117487-60117496 chr12:60117487-60117496 chr12:60117485-60117498 chr12:60117487-60117498 chr12:60117487-60117496 chr12:60117485-60117496 chr12:60117487-60117496
17	CEBPB	chr12:60130596-60131067	Hela-S3	cervix:	n/a	n/a
18	CEBPB	chr12:60107367-60107613	HepG2	liver:	n/a	chr12:60107500-60107511 chr12:60107498-60107509
19	CEBPB	chr12:60130568-60131091	IMR90	lung:	n/a	n/a
20	CEBPB	chr12:60190709-60190882	A549	lung:	n/a	chr12:60190769-60190780
21	CEBPB	chr12:60190635-60190912	HepG2	liver:	n/a	chr12:60190769-60190780
22	CEBPB	chr12:60167068-60167230	HepG2	liver:	n/a	chr12:60167176-60167187
23	CEBPB	chr12:60093475-60093729	ECC-1	luminal epithelium:	n/a	chr12:60093595-60093606
24	CEBPB	chr12:60118176-60118377	A549	lung:	n/a	chr12:60118258-60118269
25	CEBPB	chr12:60093441-60093770	HepG2	liver:	n/a	chr12:60093595-60093606
26	CEBPB	chr12:60131971-60132334	IMR90	lung:	n/a	chr12:60132140-60132151 chr12:60132141-60132152
27	CEBPB	chr12:60118090-60118454	HepG2	liver:	n/a	chr12:60118258-60118269
28	CEBPB	chr12:60117231-60117709	MCF-7	breast:	n/a	chr12:60117487-60117496 chr12:60117487-60117496 chr12:60117485-60117498 chr12:60117579-60117590 chr12:60117487-60117498 chr12:60117487-60117496 chr12:60117485-60117496 chr12:60117487-60117496
29	CEBPB	chr12:60092466-60092741	A549	lung:	n/a	n/a
30	CEBPB	chr12:60107344-60107645	H1-hESC	embryonic stem cell:	n/a	chr12:60107500-60107511 chr12:60107498-60107509
31	CEBPB	chr12:60190660-60190908	IMR90	lung:	n/a	chr12:60190769-60190780
32	CEBPB	chr12:60117317-60117666	HepG2	liver:	n/a	chr12:60117487-60117496 chr12:60117487-60117496 chr12:60117485-60117498 chr12:60117579-60117590 chr12:60117487-60117498 chr12:60117487-60117496 chr12:60117485-60117496 chr12:60117487-60117496
33	CEBPB	chr12:60193571-60193636	A549	lung:	n/a	n/a
34	CEBPB	chr12:60093380-60093773	MCF-7	breast:	n/a	chr12:60093595-60093606
35	CEBPB	chr12:60131991-60132319	HepG2	liver:	n/a	chr12:60132140-60132151 chr12:60132141-60132152
36	CEBPB	chr12:60130573-60131013	MCF-7	breast:	n/a	n/a
37	CEBPB	chr12:60089194-60089528	Hela-S3	cervix:	n/a	n/a
38	CEBPB	chr12:60107358-60107634	MCF-7	breast:	n/a	chr12:60107500-60107511 chr12:60107498-60107509
39	CEBPB	chr12:60092391-60092810	Hela-S3	cervix:	n/a	n/a
40	CHD1	chr12:60093128-60093960	IMR90	lung:	n/a	n/a
41	CHD2	chr12:60190427-60190459	GM12878	blood:	n/a	n/a
42	CTCF	chr12:60202237-60202401	Fibrobl	skin:	n/a	chr12:60202281-60202302 chr12:60202286-60202304 chr12:60202291-60202299
43	CTCF	chr12:60202240-60202390	HL-60	blood:	n/a	chr12:60202281-60202302 chr12:60202286-60202304 chr12:60202291-60202299
44	CTCF	chr12:60174660-60174810	Caco-2	colon:	n/a	n/a
45	CTCF	chr12:60202160-60202310	GM12864	blood:	n/a	chr12:60202281-60202302 chr12:60202286-60202304 chr12:60202291-60202299
46	CTCF	chr12:60202148-60202462	HUVEC	blood vessel:	n/a	chr12:60202281-60202302 chr12:60202286-60202304 chr12:60202291-60202299
47	CTCF	chr12:60174600-60174750	GM12872	blood:	n/a	n/a
48	CTCF	chr12:60202223-60202408	ProgFib	skin:	n/a	chr12:60202281-60202302 chr12:60202286-60202304 chr12:60202291-60202299
49	CTCF	chr12:60174620-60174770	AG10803	skin:	n/a	n/a
50	CTCF	chr12:60174640-60174790	NHEK	skin:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:60174815-60174865	NT2-D1	testis:	n/a
2	chr12:60091171-60091221	ECC-1	luminal epithelium:	n/a
3	chr12:60174815-60174865	HCF	heart:	n/a
4	chr12:60174815-60174865	HUVEC	blood vessel:	n/a
5	chr12:60174815-60174865	BE2_C	brain:	n/a
6	chr12:60145067-60145117	GM06990	blood:	n/a
7	chr12:60130454-60130504	NHDF-neo	bronchial:	n/a
8	chr12:60091171-60091221	SKMC	muscle:	n/a
9	chr12:60130454-60130504	ECC-1	luminal epithelium:	n/a
10	chr12:60174815-60174865	HL-60	blood:	n/a
11	chr12:60130454-60130504	BE2_C	brain:	n/a
12	chr12:60145067-60145117	ovcar-3	ovarian:	n/a
13	chr12:60145067-60145117	HIPEpiC	eye:	n/a
14	chr12:60145067-60145117	NB4	blood:	n/a
15	chr12:60091171-60091221	RPTEC	kidney:	n/a
16	chr12:60174815-60174865	BJ	skin:	n/a
17	chr12:60174815-60174865	HCPEpiC	choroid plexus:	n/a
18	chr12:60130454-60130504	HEEpiC	esophagus:	n/a
19	chr12:60130454-60130504	AG09309	skin:	n/a
20	chr12:60130454-60130504	AG10803	skin:	n/a
21	chr12:60091171-60091221	HRCEpiC	kidney:	n/a
22	chr12:60174815-60174865	HRCEpiC	kidney:	n/a
23	chr12:60145067-60145117	ProgFib	skin:	n/a
24	chr12:60130454-60130504	Caco-2	colon:	n/a
25	chr12:60174815-60174865	ECC-1	luminal epithelium:	n/a
26	chr12:60145067-60145117	Hela-S3	cervix:	n/a
27	chr12:60174815-60174865	HCM	heart:	n/a
28	chr12:60174815-60174865	PANC-1	pancreas:	n/a
29	chr12:60091171-60091221	GM19239	blood:	n/a
30	chr12:60174815-60174865	H1-hESC	embryonic stem cell:	embryo
31	chr12:60130454-60130504	HCM	heart:	n/a
32	chr12:60091171-60091221	Caco-2	colon:	n/a
33	chr12:60091171-60091221	MCF-7	breast:	n/a
34	chr12:60130454-60130504	CMK	blood:	n/a
35	chr12:60091171-60091221	HCF	heart:	n/a
36	chr12:60130454-60130504	HIPEpiC	eye:	n/a
37	chr12:60130454-60130504	NT2-D1	testis:	n/a
38	chr12:60145067-60145117	HNPCEpiC	eye:	n/a
39	chr12:60130454-60130504	LNCaP	prostate:	n/a
40	chr12:60145067-60145117	HEK293	kidney:	embryo
41	chr12:60130454-60130504	AG04449	skin:	fetal
42	chr12:60130454-60130504	HMEC	breast:	n/a
43	chr12:60130454-60130504	ovcar-3	ovarian:	n/a
44	chr12:60091171-60091221	HCPEpiC	choroid plexus:	n/a
45	chr12:60145067-60145117	NT2-D1	testis:	n/a
46	chr12:60145067-60145117	Caco-2	colon:	n/a
47	chr12:60130454-60130504	U87	brain:	n/a
48	chr12:60091171-60091221	MCF10A-Er-Src	breast:	n/a
49	chr12:60174815-60174865	HPAEpiC	pulmonary alveolar:	n/a
50	chr12:60145067-60145117	Hepatocyte	liver:	n/a

No.	Distal block	Cell Line	Cell type
1	chr12:60111151..60114974-chr12:60115302..60118048,3	MCF-7	breast:
2	chr12:60118954..60121545-chr2:160471632..160473698,2	MCF-7	breast:
3	chr12:60118809..60120952-chr12:60126355..60129129,2	MCF-7	breast:
4	chr12:59838603..59839620-chr12:60174016..60175145,3	MCF-7	breast:
5	chr12:59825209..59825865-chr12:60201866..60202550,2	MCF-7	breast:
6	chr12:60017381..60019392-chr12:60100051..60102873,2	MCF-7	breast:
7	chr12:60163187..60165402-chr12:60167180..60169412,2	K562	blood:
8	chr12:49657827..49660167-chr12:60098296..60100510,2	MCF-7	breast:
9	chr12:60163187..60165402-chr12:60167180..60169412,2	K562	blood:
10	chr12:60097757..60100206-chr12:60101491..60103766,2	MCF-7	breast:
11	chr12:34098184..34100062-chr12:60091369..60093533,4	MCF-7	breast:
12	chr12:49658095..49659753-chr12:60101910..60104297,2	MCF-7	breast:
13	chr12:60097757..60100206-chr12:60101491..60103766,2	MCF-7	breast:
14	chr12:34097991..34100054-chr12:60091596..60093323,2	MCF-7	breast:
15	chr12:60118809..60120952-chr12:60126355..60129129,2	MCF-7	breast:
16	chr12:59824786..59825486-chr12:60174654..60175192,2	MCF-7	breast:
17	chr12:60175752..60177961-chr12:60179247..60181650,2	K562	blood:
18	chr12:60113980..60116792-chr12:60129160..60132180,3	MCF-7	breast:
19	chr12:60201872..60202711-chr12:60228771..60229623,3	MCF-7	breast:
20	chr12:60113980..60116792-chr12:60129160..60132180,3	MCF-7	breast:
21	chr12:60175752..60177961-chr12:60179247..60181650,2	K562	blood:
22	chr12:49657670..49659344-chr12:60094234..60097237,3	MCF-7	breast:
23	chr12:49658530..49660065-chr12:60117351..60120020,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RP11-272B17.2.1-2	chr12:60113479-60113725	NONHSAT029055

Variant related genes	Relation type
ENSG00000257146	TF binding region
ENSG00000237176	TF binding region
SLC16A7	TF binding region
ENSG00000257146	CpG island
ENSG00000237176	CpG island
SLC16A7	CpG island
ENSG00000167553	chromatin interactions
ENSG00000258101	chromatin interactions
ENSG00000123636	chromatin interactions
ENSG00000224152	chromatin interactions
ENSG00000257146	chromatin interactions

Extended variants
information (count: 4674 )
Associated
traits (count: 84 )

Variant overlapped rSNPs/rCNVs (count:4674 , 50 per page) page: 1 2 3 4 5 6 7 ... 94

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1795886	chr12:60087572-60087573	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs138896000	chr12:60087635-60087636	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs550487209	chr12:60087646-60087647	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs556608240	chr12:60087664-60087665	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs576552888	chr12:60087696-60087697	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs545547645	chr12:60087740-60087741	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs149401892	chr12:60087747-60087748	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs143736217	chr12:60087777-60087778	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs544313618	chr12:60087787-60087788	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs138375404	chr12:60087855-60087856	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs530774365	chr12:60087857-60087858	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs544636502	chr12:60087863-60087864	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs564525087	chr12:60087868-60087869	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs570149748	chr12:60087887-60087888	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs539252471	chr12:60087925-60087926	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs377309964	chr12:60087938-60087939	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs76428362	chr12:60087947-60087948	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs547154902	chr12:60087960-60087961	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs371399702	chr12:60087965-60087966	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs376268162	chr12:60087989-60087990	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs549396668	chr12:60088132-60088133	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs143872100	chr12:60088196-60088197	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs188458650	chr12:60088230-60088231	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs10459250	chr12:60088247-60088248	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs147249860	chr12:60088254-60088255	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs140685145	chr12:60088255-60088256	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs552677445	chr12:60088258-60088259	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs141789453	chr12:60088263-60088264	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs36007991	chr12:60088272-60088273	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs550699575	chr12:60088299-60088300	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs34345196	chr12:60088317-60088318	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs547250782	chr12:60088330-60088331	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs150578511	chr12:60088336-60088337	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs113916152	chr12:60088351-60088352	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs139593766	chr12:60088381-60088382	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs181605670	chr12:60088405-60088406	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs534104139	chr12:60088424-60088425	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs35936695	chr12:60088427-60088428	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs186579715	chr12:60088576-60088577	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs538580539	chr12:60088601-60088602	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs543855505	chr12:60088615-60088616	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs540710534	chr12:60088628-60088629	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs560671589	chr12:60088637-60088638	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs529433085	chr12:60088797-60088798	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs190650573	chr12:60088840-60088841	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs182331604	chr12:60088867-60088868	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs532043487	chr12:60088871-60088872	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs546024761	chr12:60088880-60088881	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs551700091	chr12:60088892-60088893	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs374172712	chr12:60088895-60088896	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:84)

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
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Neurodevelopmental disorder	22521361	CNVD
T-cell prolymphocytic leukemia	19278963	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
Lissencephaly	21572526	CNVD
Lung cancer	18438408	CNVD
Breast cancer	19602461	CNVD
Breast cancer	17899364	CNVD
Colorectal cancer	16272173	CNVD
Prostate cancer	18632612	CNVD
Metanephric adenoma	20802469	CNVD
Glioblastoma multiforme	17387387	CNVD
liposarcomas	17372913	CNVD
Non-small cell lung cancer	24170126	CNVD
Cancer	16751803	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	21785460	CNVD
small cell lung cancer	20016488	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Hodgkin''s lymphoma	18179710	CNVD
Urothelial cell carcinoma	18451213	CNVD
Melanoma	18172304	CNVD
Glioblastoma multiforme	21390271	CNVD
Cancer	20164919	CNVD
Leukemia	18628472	CNVD
Glioblastoma multiforme	22291905	CNVD
Glioblastoma multiforme	19435819	CNVD
Myelofibrosis	22110671	CNVD
Phyllodes tumor	17334353	CNVD
Glaucoma	21310917	CNVD
Breast cancer	16272173	CNVD
Mental retardation	19951919	CNVD
Glaucoma	21447600	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Developmental delay	21267005	CNVD
12q14 microdeletion syndrome	21267005	CNVD
Developmental delay	19277063	CNVD
Dwarfism	19277063	CNVD
Fibroblasts	20926602	CNVD
Follicular lymphoma	18703704	CNVD
Acute myeloid leukemia	21251322	CNVD
Glioblastoma multiforme	20080666	CNVD
Medulloblastoma	19270706	CNVD
Breast cancer	17133270	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Glioblastoma	17090523	CNVD
Multiple myeloma	16616336	CNVD
Lung cancer	16773561	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Breast cancer	21364760	CNVD
Schizophrenia	23813976	CNVD
Osteosarcoma	21215367	CNVD

Chromatin state (count:729 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:60026600-60089200	Weak transcription	Gastric	stomach
2	chr12:60045800-60099800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
3	chr12:60050800-60098600	Weak transcription	Primary T cells fromperipheralblood	blood
4	chr12:60069600-60131400	Weak transcription	Primary T helper cells fromperipheralblood	blood
5	chr12:60071600-60098600	Weak transcription	Primary T helper cells PMA-I stimulated	--
6	chr12:60072200-60098600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
7	chr12:60072800-60098000	Weak transcription	Primary B cells from peripheral blood	blood
8	chr12:60073000-60089000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
9	chr12:60084400-60090800	Weak transcription	Fetal Heart	heart
10	chr12:60085200-60098600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
11	chr12:60086000-60088200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
12	chr12:60086000-60102400	Weak transcription	Primary T cells from cord blood	blood
13	chr12:60086200-60087800	Weak transcription	NHDF-Ad	bronchial
14	chr12:60086200-60088800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
15	chr12:60086200-60089000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
16	chr12:60086200-60089000	Weak transcription	Left Ventricle	heart
17	chr12:60086200-60098400	Weak transcription	Primary B cells from cord blood	blood
18	chr12:60086200-60105200	Weak transcription	Aorta	Aorta
19	chr12:60086200-60106400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
20	chr12:60087400-60087600	Enhancers	Primary T killer naive cells fromperipheralblood	blood
21	chr12:60087600-60108000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
22	chr12:60087800-60088000	Enhancers	NHDF-Ad	bronchial
23	chr12:60088000-60088400	Weak transcription	NHDF-Ad	bronchial
24	chr12:60088200-60093600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
25	chr12:60088400-60093400	Enhancers	NHDF-Ad	bronchial
26	chr12:60088800-60089800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
27	chr12:60089000-60089400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
28	chr12:60089000-60089400	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
29	chr12:60089000-60089400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
30	chr12:60089000-60089400	Enhancers	Left Ventricle	heart
31	chr12:60089000-60089400	Enhancers	HSMM	muscle
32	chr12:60089000-60089400	Enhancers	NHLF	lung
33	chr12:60089000-60089600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
34	chr12:60089000-60089600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
35	chr12:60089000-60089600	Enhancers	Muscle Satellite Cultured Cells	--
36	chr12:60089000-60089600	Enhancers	Right Atrium	heart
37	chr12:60089000-60089600	Enhancers	NHEK	skin
38	chr12:60089000-60089600	Enhancers	Osteobl	bone
39	chr12:60089200-60089600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
40	chr12:60089200-60089600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
41	chr12:60089200-60089600	Enhancers	HMEC	breast
42	chr12:60089400-60089600	Enhancers	Gastric	stomach
43	chr12:60089400-60092200	Weak transcription	NHLF	lung
44	chr12:60089400-60093200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
45	chr12:60089400-60093600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
46	chr12:60089400-60093800	Weak transcription	HSMM	muscle
47	chr12:60089400-60126000	Weak transcription	Left Ventricle	heart
48	chr12:60089600-60092000	Weak transcription	Osteobl	bone
49	chr12:60089600-60092200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
50	chr12:60089600-60092200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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