Variant report

Variant	esv1841396
Chromosome Location	chr12:82768717-82881082
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	chr12:82777813-82777956	K562	blood:	n/a	n/a
2	ATF2	chr12:82832100-82832603	GM12878	blood:	n/a	n/a
3	ATF2	chr12:82832115-82832546	GM12878	blood:	n/a	n/a
4	BATF	chr12:82832252-82832436	GM12878	blood:	n/a	n/a
5	BATF	chr12:82832164-82832441	GM12878	blood:	n/a	n/a
6	BATF	chr12:82834677-82835020	GM12878	blood:	n/a	n/a
7	BATF	chr12:82875848-82876058	GM12878	blood:	n/a	chr12:82875962-82875973
8	BATF	chr12:82875809-82876048	GM12878	blood:	n/a	chr12:82875962-82875973
9	BCL11A	chr12:82832196-82832545	GM12878	blood:	n/a	n/a
10	BHLHE40	chr12:82831707-82831734	GM12878	blood:	n/a	n/a
11	BRCA1	chr12:82801795-82801840	Hela-S3	cervix:	n/a	n/a
12	CEBPB	chr12:82873507-82873707	H1-hESC	embryonic stem cell:	n/a	n/a
13	CEBPB	chr12:82874400-82874679	A549	lung:	n/a	chr12:82874489-82874500
14	CEBPB	chr12:82820994-82821120	A549	lung:	n/a	n/a
15	CEBPB	chr12:82873334-82873694	IMR90	lung:	n/a	n/a
16	CEBPB	chr12:82781567-82781769	A549	lung:	n/a	chr12:82781661-82781672
17	CEBPB	chr12:82874485-82874521	K562	blood:	n/a	chr12:82874489-82874500
18	CEBPB	chr12:82856636-82856920	HepG2	liver:	n/a	chr12:82856766-82856777
19	CEBPB	chr12:82848538-82848873	HepG2	liver:	n/a	n/a
20	CEBPB	chr12:82856754-82856805	K562	blood:	n/a	chr12:82856766-82856777
21	CEBPB	chr12:82874327-82874641	HepG2	liver:	n/a	chr12:82874489-82874500
22	CEBPB	chr12:82801187-82801811	Hela-S3	cervix:	n/a	chr12:82801447-82801460
23	CEBPB	chr12:82879296-82879550	MCF-7	breast:	n/a	n/a
24	CEBPB	chr12:82781498-82781821	HepG2	liver:	n/a	chr12:82781661-82781672
25	CEBPB	chr12:82873364-82873752	MCF-7	breast:	n/a	n/a
26	CEBPB	chr12:82862631-82862998	HepG2	liver:	n/a	n/a
27	CEBPB	chr12:82873331-82873689	MCF-7	breast:	n/a	n/a
28	CEBPB	chr12:82781509-82781761	IMR90	lung:	n/a	chr12:82781661-82781672
29	CHD1	chr12:82781859-82781861	GM12878	blood:	n/a	n/a
30	CHD1	chr12:82831872-82831963	GM12878	blood:	n/a	n/a
31	CREB1	chr12:82832269-82832541	GM12878	blood:	n/a	n/a
32	CREB1	chr12:82832106-82832606	GM12878	blood:	n/a	n/a
33	CTCF	chr12:82777840-82777990	HEEpiC	esophagus:	n/a	chr12:82777870-82777891 chr12:82777868-82777886
34	CTCF	chr12:82777828-82777967	HepG2	liver:	n/a	chr12:82777870-82777891 chr12:82777868-82777886
35	CTCF	chr12:82864953-82865182	H1-hESC	embryonic stem cell:	n/a	chr12:82865069-82865082 chr12:82865068-82865089 chr12:82865071-82865079
36	CTCF	chr12:82777760-82777910	K562	blood:	n/a	chr12:82777870-82777891 chr12:82777868-82777886
37	CTCF	chr12:82777760-82777910	GM12870	blood:	n/a	chr12:82777870-82777891 chr12:82777868-82777886
38	CTCF	chr12:82777760-82777910	HL-60	blood:	n/a	chr12:82777870-82777891 chr12:82777868-82777886
39	CTCF	chr12:82777800-82777950	SK-N-SH_RA	brain:	n/a	chr12:82777870-82777891 chr12:82777868-82777886
40	CTCF	chr12:82777820-82777970	HMEC	breast:	n/a	chr12:82777870-82777891 chr12:82777868-82777886
41	CTCF	chr12:82777774-82777958	GM10248	blood:	n/a	chr12:82777870-82777891 chr12:82777868-82777886
42	CTCF	chr12:82777780-82777930	HPAF	blood vessel:	n/a	chr12:82777870-82777891 chr12:82777868-82777886
43	CTCF	chr12:82777791-82777941	K562	blood:	n/a	chr12:82777870-82777891 chr12:82777868-82777886
44	CTCF	chr12:82777785-82777949	GM10266	blood:	n/a	chr12:82777870-82777891 chr12:82777868-82777886
45	CTCF	chr12:82777820-82777970	GM12864	blood:	n/a	chr12:82777870-82777891 chr12:82777868-82777886
46	CTCF	chr12:82777760-82777910	GM12872	blood:	n/a	chr12:82777870-82777891 chr12:82777868-82777886
47	CTCF	chr12:82777780-82777930	GM12878	blood:	n/a	chr12:82777870-82777891 chr12:82777868-82777886
48	CTCF	chr12:82777960-82778110	GM12868	blood:	n/a	n/a
49	CTCF	chr12:82777840-82777990	AG09309	skin:	n/a	chr12:82777870-82777891 chr12:82777868-82777886
50	CTCF	chr12:82865040-82865190	MCF-7	breast:	n/a	chr12:82865069-82865082 chr12:82865068-82865089 chr12:82865071-82865079

No.	Distal block	Cell Line	Cell type
1	chr12:82752158..82753744-chr12:82806629..82809216,2	K562	blood:
2	chr12:82864287..82866811-chr3:130394292..130397010,2	MCF-7	breast:
3	chr12:82855086..82857984-chr12:82863232..82865138,2	MCF-7	breast:
4	chr12:82751683..82753749-chr12:82770404..82772509,2	MCF-7	breast:
5	chr12:82805259..82807721-chr12:82854362..82856467,2	MCF-7	breast:
6	chr12:82801364..82803127-chr12:82805728..82808157,3	MCF-7	breast:
7	chr12:82750803..82753680-chr12:82768474..82770672,2	MCF-7	breast:
8	chr12:80083780..80085880-chr12:82769825..82772060,2	MCF-7	breast:
9	chr12:82853805..82855324-chr12:82862383..82864290,2	MCF-7	breast:
10	chr12:82795159..82796748-chr12:82799968..82802561,2	MCF-7	breast:
11	chr12:82853805..82855324-chr12:82862383..82864290,2	MCF-7	breast:
12	chr12:82855086..82857984-chr12:82863232..82865138,2	MCF-7	breast:
13	chr12:82801364..82803127-chr12:82805728..82808157,3	MCF-7	breast:
14	chr12:82819815..82822098-chr12:82840091..82842622,2	MCF-7	breast:
15	chr12:82818588..82822446-chr12:82827845..82830873,3	MCF-7	breast:
16	chr12:82795159..82796748-chr12:82799968..82802561,2	MCF-7	breast:
17	chr12:82805259..82807721-chr12:82854362..82856467,2	MCF-7	breast:
18	chr12:82749238..82752209-chr12:82805910..82807639,2	MCF-7	breast:
19	chr12:82777410..82778076-chr12:83021381..83021922,3	MCF-7	breast:
20	chr12:82818588..82822446-chr12:82827845..82830873,3	MCF-7	breast:
21	chr12:82819815..82822098-chr12:82840091..82842622,2	MCF-7	breast:
22	chr12:82753358..82755104-chr12:82772991..82774509,2	K562	blood:
23	chr12:82777578..82778449-chr12:82911138..82912044,4	MCF-7	breast:
24	chr12:82750490..82752640-chr12:82799108..82801602,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CCDC59-2	chr12:82875739-82875807	ENSG00000258170.1
2	lnc-CCDC59-2	chr12:82874897-82875259	ENSG00000258170.1
3	lnc-TMTC2-4	chr12:82862235-82862727	NONHSAT029720

Variant related genes	Relation type
ENSG00000257875	TF binding region
METTL25	TF binding region
ENSG00000258048	chromatin interactions
ENSG00000133773	chromatin interactions
ENSG00000127720	chromatin interactions
ENSG00000177425	chromatin interactions

Extended variants
information (count: 4156 )
Associated
traits (count: 67 )

Variant overlapped rSNPs/rCNVs (count:4156 , 50 per page) page: 1 2 3 4 5 6 7 ... 84

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2895912	chr12:82768717-82768718	Strong transcription Weak transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs534303827	chr12:82768720-82768721	Strong transcription Weak transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs370325340	chr12:82768726-82768727	Strong transcription Weak transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs373982038	chr12:82768741-82768742	Strong transcription Weak transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs546316510	chr12:82768784-82768785	Strong transcription Weak transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs543584753	chr12:82768830-82768831	Strong transcription Weak transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs568058739	chr12:82768888-82768889	Strong transcription Weak transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs536086765	chr12:82768901-82768902	Strong transcription Weak transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs180868811	chr12:82768965-82768966	Strong transcription Weak transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs575894509	chr12:82768974-82768975	Strong transcription Weak transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs540107895	chr12:82768986-82768987	Strong transcription Weak transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs558196978	chr12:82769019-82769020	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs573308027	chr12:82769044-82769045	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs2895911	chr12:82769045-82769046	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs371871326	chr12:82769067-82769068	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs574012826	chr12:82769092-82769093	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs376865975	chr12:82769148-82769149	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs542013304	chr12:82769150-82769151	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs35134877	chr12:82769182-82769183	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs371735882	chr12:82769211-82769212	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs201760921	chr12:82769221-82769222	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs144093930	chr12:82769222-82769223	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs563311856	chr12:82769229-82769230	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs79124987	chr12:82769231-82769232	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs67299552	chr12:82769232-82769233	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs11334363	chr12:82769233-82769234	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs530849885	chr12:82769235-82769236	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs2401033	chr12:82769238-82769239	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs386764712	chr12:82769244-82769245	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs564018865	chr12:82769270-82769271	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs528120633	chr12:82769279-82769280	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs546178615	chr12:82769323-82769324	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs568157226	chr12:82769335-82769336	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs186506444	chr12:82769583-82769584	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs2401032	chr12:82769630-82769631	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs147111981	chr12:82769641-82769642	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs373460258	chr12:82769671-82769672	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs377710215	chr12:82769682-82769683	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs4417379	chr12:82769700-82769701	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs4257045	chr12:82769711-82769712	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs56721382	chr12:82769713-82769714	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs555431404	chr12:82769734-82769735	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs191368678	chr12:82769852-82769853	Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
44	rs544345469	chr12:82769858-82769859	Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
45	rs556605410	chr12:82769864-82769865	Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
46	rs117185507	chr12:82769901-82769902	Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
47	rs545588624	chr12:82769909-82769910	Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
48	rs181635645	chr12:82769931-82769932	Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
49	rs528326573	chr12:82769942-82769943	Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
50	rs530907336	chr12:82769979-82769980	Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:67)

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
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
abnormal development	18461090	CNVD
Prostate cancer	18632612	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	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
Malignant peripheral nerve sheath tumor	18522746	CNVD
Ovarian cancer	21720365	CNVD
Breast cancer	21364760	CNVD
Acute myeloid leukemia	20729466	CNVD
Myelofibrosis	22110671	CNVD
Colorectal cancer	16272173	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Renal cell carcinoma	18194544	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:914 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:82753400-82786200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
2	chr12:82753600-82777800	Weak transcription	Rectal Smooth Muscle	rectum
3	chr12:82753600-82782400	Weak transcription	Monocytes-CD14+_RO01746	blood
4	chr12:82753600-82799800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
5	chr12:82753600-82805200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
6	chr12:82753800-82770800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
7	chr12:82753800-82804800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
8	chr12:82754000-82794800	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
9	chr12:82754000-82804600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
10	chr12:82754200-82769000	Weak transcription	Cortex derived primary cultured neurospheres	brain
11	chr12:82754200-82779600	Weak transcription	Brain Inferior Temporal Lobe	brain
12	chr12:82754200-82803600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
13	chr12:82754400-82782200	Weak transcription	Primary T helper cells PMA-I stimulated	--
14	chr12:82754400-82804000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
15	chr12:82754600-82782200	Weak transcription	Duodenum Smooth Muscle	Duodenum
16	chr12:82754600-82794600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
17	chr12:82755600-82802200	Weak transcription	Pancreas	Pancrea
18	chr12:82755800-82782400	Weak transcription	Gastric	stomach
19	chr12:82758200-82782400	Weak transcription	Ovary	ovary
20	chr12:82758400-82795800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
21	chr12:82758400-82835600	Weak transcription	Psoas Muscle	Psoas
22	chr12:82758600-82777000	Weak transcription	Fetal Heart	heart
23	chr12:82758600-82799600	Weak transcription	Skeletal Muscle Male	skeletal muscle
24	chr12:82761600-82790600	Weak transcription	Brain Anterior Caudate	brain
25	chr12:82761800-82792000	Weak transcription	Stomach Mucosa	stomach
26	chr12:82764000-82782400	Weak transcription	Brain Cingulate Gyrus	brain
27	chr12:82764000-82801400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
28	chr12:82764200-82794000	Weak transcription	Placenta	Placenta
29	chr12:82764400-82769600	Weak transcription	Fetal Thymus	thymus
30	chr12:82765200-82779600	Weak transcription	Right Ventricle	heart
31	chr12:82765600-82769600	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
32	chr12:82767200-82768800	Strong transcription	Adipose Nuclei	Adipose
33	chr12:82767200-82769200	ZNF genes & repeats	Aorta	Aorta
34	chr12:82767400-82769200	ZNF genes & repeats	Primary Natural Killer cells fromperipheralblood	blood
35	chr12:82767400-82769800	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
36	chr12:82767600-82768800	ZNF genes & repeats	Primary T helper cells fromperipheralblood	blood
37	chr12:82767600-82769200	ZNF genes & repeats	Primary B cells from peripheral blood	blood
38	chr12:82767800-82769200	ZNF genes & repeats	Fetal Muscle Leg	muscle
39	chr12:82767800-82769200	Strong transcription	Skeletal Muscle Female	skeletal muscle
40	chr12:82768000-82769600	Strong transcription	Primary B cells from cord blood	blood
41	chr12:82768000-82782200	Weak transcription	Left Ventricle	heart
42	chr12:82768000-82791000	Weak transcription	Brain Angular Gyrus	brain
43	chr12:82768200-82769000	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
44	chr12:82768200-82769000	Strong transcription	Breast Myoepithelial Primary Cells	Breast
45	chr12:82768200-82769000	Weak transcription	Liver	Liver
46	chr12:82768200-82769000	Weak transcription	Rectal Mucosa Donor 29	rectum
47	chr12:82768200-82769400	ZNF genes & repeats	Primary T cells from cord blood	blood
48	chr12:82768200-82782200	Weak transcription	Fetal Lung	lung
49	chr12:82768200-82782200	Weak transcription	Sigmoid Colon	Sigmoid Colon
50	chr12:82768200-82786200	Weak transcription	Fetal Intestine Large	intestine

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