Variant report

Variant	esv1817813
Chromosome Location	chr12:8346318-8379082
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:100)
CpG islands
(count:916)
Chromatin interactive
region (count:1)
LncRNA
region (count:23)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:100 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr12:8371647-8371788	H1-hESC	embryonic stem cell:	n/a	n/a
2	CEBPB	chr12:8350455-8350821	HCT-116	colon:	n/a	n/a
3	CEBPB	chr12:8350546-8350745	K562	blood:	n/a	n/a
4	CEBPB	chr12:8350554-8350655	A549	lung:	n/a	n/a
5	CEBPB	chr12:8350634-8350826	K562	blood:	n/a	n/a
6	CEBPB	chr12:8350339-8350909	IMR90	lung:	n/a	n/a
7	CEBPB	chr12:8350414-8350907	Hela-S3	cervix:	n/a	n/a
8	CTCF	chr12:8352660-8352810	GM12873	blood:	n/a	chr12:8352744-8352762 chr12:8352739-8352760
9	CTCF	chr12:8352746-8352782	MCF-7	breast:	n/a	n/a
10	CTCF	chr12:8348320-8348470	HBMEC	blood vessel:	n/a	n/a
11	CTCF	chr12:8352700-8352850	GM12866	blood:	n/a	chr12:8352744-8352762 chr12:8352739-8352760
12	CTCF	chr12:8348300-8348450	GM06990	blood:	n/a	n/a
13	CTCF	chr12:8352700-8352850	HCPEpiC	choroid plexus:	n/a	chr12:8352744-8352762 chr12:8352739-8352760
14	CTCF	chr12:8352700-8352850	HEK293	kidney:	n/a	chr12:8352744-8352762 chr12:8352739-8352760
15	CTCF	chr12:8348460-8348610	GM12873	blood:	n/a	n/a
16	CTCF	chr12:8352620-8352770	GM12871	blood:	n/a	chr12:8352744-8352762 chr12:8352739-8352760
17	CTCF	chr12:8352580-8352730	HMF	breast:	n/a	n/a
18	CTCF	chr12:8371821-8372126	K562	blood:	n/a	n/a
19	CTCF	chr12:8371828-8372079	K562	blood:	n/a	n/a
20	CTCF	chr12:8348280-8348430	HMF	breast:	n/a	n/a
21	CTCF	chr12:8348300-8348450	GM12873	blood:	n/a	n/a
22	CTCF	chr12:8352700-8352850	AG04449	skin:	n/a	chr12:8352744-8352762 chr12:8352739-8352760
23	CTCF	chr12:8348240-8348390	HRE	kidney:	n/a	n/a
24	CTCF	chr12:8352741-8352782	GM10266	blood:	n/a	chr12:8352744-8352762
25	CTCF	chr12:8348280-8348430	AG04449	skin:	n/a	n/a
26	CTCF	chr12:8372082-8372178	GM10266	blood:	n/a	n/a
27	CTCF	chr12:8352640-8352790	HPAF	blood vessel:	n/a	chr12:8352744-8352762 chr12:8352739-8352760
28	CTCF	chr12:8352665-8352829	K562	blood:	n/a	chr12:8352744-8352762 chr12:8352739-8352760
29	CTCF	chr12:8352680-8352830	AG04450	lung:	n/a	chr12:8352744-8352762 chr12:8352739-8352760
30	CTCF	chr12:8352600-8352750	BJ	skin:	n/a	n/a
31	CTCF	chr12:8348220-8348370	HCT-116	colon:	n/a	n/a
32	CTCF	chr12:8348220-8348370	HL-60	blood:	n/a	n/a
33	CTCF	chr12:8352740-8352890	GM12873	blood:	n/a	chr12:8352744-8352762
34	CTCF	chr12:8347493-8347518	GM10248	blood:	n/a	n/a
35	CTCF	chr12:8350760-8350934	K562	blood:	n/a	n/a
36	CTCF	chr12:8352640-8352790	HepG2	liver:	n/a	chr12:8352744-8352762 chr12:8352739-8352760
37	CTCF	chr12:8352640-8352790	GM12867	blood:	n/a	chr12:8352744-8352762 chr12:8352739-8352760
38	CTCF	chr12:8348220-8348370	AoAF	blood vessel:	n/a	n/a
39	CTCF	chr12:8366831-8366895	Lung_OC	lung:	n/a	n/a
40	CTCF	chr12:8348260-8348410	A549	lung:	n/a	n/a
41	CTCF	chr12:8352548-8352857	A549	lung:	n/a	chr12:8352744-8352762 chr12:8352739-8352760
42	CTCF	chr12:8352680-8352830	HA-sp	spinal cord:	n/a	chr12:8352744-8352762 chr12:8352739-8352760
43	CTCF	chr12:8348340-8348490	AoAF	blood vessel:	n/a	n/a
44	CTCF	chr12:8352680-8352830	GM12872	blood:	n/a	chr12:8352744-8352762 chr12:8352739-8352760
45	CTCF	chr12:8350760-8350979	K562	blood:	n/a	n/a
46	CTCF	chr12:8350759-8351025	K562	blood:	n/a	n/a
47	CTCF	chr12:8348240-8348390	AG04450	lung:	n/a	n/a
48	CTCF	chr12:8352680-8352830	GM12875	blood:	n/a	chr12:8352744-8352762 chr12:8352739-8352760
49	CTCF	chr12:8348300-8348450	HPAF	blood vessel:	n/a	n/a
50	CTCF	chr12:8348280-8348430	AG09309	skin:	n/a	n/a

(count:916 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:8377808-8377858	MCF-7	breast:	n/a
2	chr12:8377808-8377858	MCF-7	breast:	n/a
3	chr12:8371626-8371676	GM06990	blood:	n/a
4	chr12:8377512-8377562	PFSK-1	brain:	n/a
5	chr12:8372478-8372528	HL-60	blood:	n/a
6	chr12:8375310-8375360	ovcar-3	ovarian:	n/a
7	chr12:8374206-8374256	HNPCEpiC	eye:	n/a
8	chr12:8378308-8378358	GM06990	blood:	n/a
9	chr12:8372478-8372528	HAEpiC	amniotic membrane:	n/a
10	chr12:8372182-8372232	AG04449	skin:	fetal
11	chr12:8375674-8375724	MCF-7	breast:	n/a
12	chr12:8377808-8377858	AG09319	gingival:	n/a
13	chr12:8371812-8371862	HNPCEpiC	eye:	n/a
14	chr12:8376943-8376993	HRCEpiC	kidney:	n/a
15	chr12:8374133-8374183	AG04450	lung:	fetal
16	chr12:8377808-8377858	HAEpiC	amniotic membrane:	n/a
17	chr12:8374133-8374183	T-47D	breast:	n/a
18	chr12:8371812-8371862	AG10803	skin:	n/a
19	chr12:8374206-8374256	NT2-D1	testis:	n/a
20	chr12:8374206-8374256	RPTEC	kidney:	n/a
21	chr12:8376090-8376140	HAEpiC	amniotic membrane:	n/a
22	chr12:8375310-8375360	T-47D	breast:	n/a
23	chr12:8375674-8375724	MCF10A-Er-Src	breast:	n/a
24	chr12:8375310-8375360	U87	brain:	n/a
25	chr12:8376090-8376140	AoSMC	blood vessel:	n/a
26	chr12:8372182-8372232	NHBE	bronchial:	n/a
27	chr12:8371924-8371974	SKMC	muscle:	n/a
28	chr12:8376090-8376140	HEEpiC	esophagus:	n/a
29	chr12:8371924-8371974	K562	blood:	n/a
30	chr12:8371812-8371862	NHDF-neo	bronchial:	n/a
31	chr12:8376090-8376140	Caco-2	colon:	n/a
32	chr12:8371812-8371862	Hela-S3	cervix:	n/a
33	chr12:8374206-8374256	ECC-1	luminal epithelium:	n/a
34	chr12:8375310-8375360	HNPCEpiC	eye:	n/a
35	chr12:8377808-8377858	SK-N-MC	brain:	n/a
36	chr12:8375674-8375724	T-47D	breast:	n/a
37	chr12:8377512-8377562	NT2-D1	testis:	n/a
38	chr12:8376090-8376140	ProgFib	skin:	n/a
39	chr12:8376943-8376993	NHBE	bronchial:	n/a
40	chr12:8375674-8375724	HUVEC	blood vessel:	n/a
41	chr12:8371924-8371974	PrEC	prostate:	n/a
42	chr12:8373953-8374003	Hela-S3	cervix:	n/a
43	chr12:8372182-8372232	Jurkat	blood:	n/a
44	chr12:8377808-8377858	GM12891	blood:	n/a
45	chr12:8378308-8378358	U87	brain:	n/a
46	chr12:8374133-8374183	HRE	kidney:	n/a
47	chr12:8372478-8372528	SK-N-MC	brain:	n/a
48	chr12:8372478-8372528	ECC-1	luminal epithelium:	n/a
49	chr12:8371812-8371862	NT2-D1	testis:	n/a
50	chr12:8377808-8377858	PANC-1	pancreas:	n/a

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr12:8377558..8379489-chr12:8392400..8395227,2	K562	blood:

(count:23 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZNF705A-1	chr12:8347325-8347392	ENSG00000226711.2
2	lnc-ZNF705A-1	chr12:8347016-8347077	ENSG00000226711.2
3	lnc-ZNF705A-1	chr12:8347026-8347077	ENSG00000226711.2
4	lnc-ZNF705A-1	chr12:8347016-8347077	ENSG00000226711.2
5	lnc-ZNF705A-1	chr12:8378905-8379047	NONHSAT026297
6	lnc-ZNF705A-1	chr12:8347325-8347392	ENSG00000226711.2
7	lnc-FAM90A1-2	chr12:8359252-8359306	NONHSAT026302
8	lnc-ZNF705A-1	chr12:8356654-8356724	ENSG00000226711.2
9	lnc-ZNF705A-1	chr12:8347873-8348008	ENSG00000226711.2
10	lnc-FAM90A1-2	chr12:8352195-8352416	NONHSAT026302
11	lnc-ZNF705A-1	chr12:8348853-8349114	ENSG00000226711.2
12	lnc-ZNF705A-1	chr12:8368402-8368631	ENSG00000226711.2
13	lnc-ZNF705A-1	chr12:8378474-8378624	NONHSAT026297
14	lnc-ZNF705A-1	chr12:8356654-8356771	ENSG00000226711.2
15	lnc-ZNF705A-1	chr12:8346800-8347077	ENSG00000226711.2
16	lnc-ZNF705A-1	chr12:8346799-8347077	NONHSAT026297
17	lnc-ZNF705A-1	chr12:8347325-8347392	ENSG00000226711.2
18	lnc-ZNF705A-1	chr12:8346799-8347077	ENSG00000226711.2
19	lnc-ZNF705A-1	chr12:8346895-8346923	ENSG00000226711.2
20	lnc-ZNF705A-1	chr12:8348853-8349114	ENSG00000226711.2
21	lnc-ZNF705A-1	chr12:8347873-8348248	ENSG00000226711.2
22	lnc-ZNF705A-1	chr12:8347529-8347872	ENSG00000226711.2
23	lnc-ZNF705A-1	chr12:8347325-8347392	ENSG00000226711.2

No data

Variant related genes	Relation type
ENSG00000244050	TF binding region
FAM66C	TF binding region
ALG1L10P	TF binding region
ENSG00000266026	TF binding region
ENSG00000244050	CpG island
FAM66C	CpG island
ALG1L10P	CpG island
ENSG00000266026	CpG island

Extended variants
information (count: 1387 )
Associated
traits (count: 79 )

Variant overlapped rSNPs/rCNVs (count:1387 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs57889102	chr12:8346340-8346341	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs10840961	chr12:8346347-8346348	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs188130138	chr12:8346439-8346440	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs192751469	chr12:8346508-8346509	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs200363220	chr12:8346569-8346570	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs201361480	chr12:8346572-8346573	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs10840962	chr12:8346608-8346609	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
8	rs200823772	chr12:8346633-8346634	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs115067723	chr12:8346697-8346698	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs563366147	chr12:8346703-8346704	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs12300783	chr12:8346795-8346796	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs114481540	chr12:8346812-8346813	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
13	rs4291750	chr12:8346866-8346867	Weak transcription Enhancers	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
14	rs4463910	chr12:8346867-8346868	Weak transcription Enhancers	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
15	rs559361083	chr12:8346891-8346892	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
16	rs184997225	chr12:8346941-8346942	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
17	rs186735076	chr12:8346960-8346961	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
18	rs4309226	chr12:8346978-8346979	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
19	rs12302282	chr12:8347013-8347014	Weak transcription	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs4293194	chr12:8347025-8347026	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
21	rs141180940	chr12:8347034-8347035	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
22	rs146962884	chr12:8347064-8347065	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
23	rs528102700	chr12:8347086-8347087	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs191604131	chr12:8347109-8347110	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs76711065	chr12:8347121-8347122	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs4565979	chr12:8347124-8347125	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs75932809	chr12:8347147-8347148	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs112171088	chr12:8347162-8347163	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs78481554	chr12:8347164-8347165	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs77826260	chr12:8347166-8347167	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs368069935	chr12:8347204-8347205	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs184733532	chr12:8347230-8347231	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs75843697	chr12:8347244-8347245	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs565212318	chr12:8347291-8347292	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs10770308	chr12:8347358-8347359	Strong transcription Weak transcription	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
36	rs143454960	chr12:8347429-8347430	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs77636294	chr12:8347495-8347496	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs80112877	chr12:8347496-8347497	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs189498680	chr12:8347528-8347529	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs181650959	chr12:8347547-8347548	Strong transcription Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
41	rs567126848	chr12:8347551-8347552	Strong transcription Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
42	rs144121911	chr12:8347583-8347584	Strong transcription Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
43	rs148285401	chr12:8347621-8347622	Strong transcription Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
44	rs7979238	chr12:8347795-8347796	Strong transcription Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
45	rs185246542	chr12:8347841-8347842	Strong transcription Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
46	rs12302649	chr12:8347870-8347871	Strong transcription Weak transcription	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs139311378	chr12:8347878-8347879	Strong transcription Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
48	rs12372760	chr12:8347953-8347954	Strong transcription Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
49	rs10770309	chr12:8347958-8347959	Strong transcription Weak transcription	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
50	rs1051570	chr12:8348133-8348134	Strong transcription Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a

Variant related diseases (count:79)

Disease	PMID	Source
Acute lymphoblastic leukemia	22237106	CNVD
Breast cancer	17133270	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Medulloblastoma	16968546	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Hepatocellular carcinoma	16750200	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
Breast cancer	22032731	CNVD
Cancer	21183584	CNVD
Myxofibrosarcoma	16751306	CNVD
Non-small cell lung cancer	21829676	CNVD
Ovarian neoplasms	16753589	CNVD
Prostate cancer	21965145	CNVD
Acute myeloid leukemia	16864856	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Disorders of sex development	21048976	CNVD
Glioblastoma multiforme	21080181	CNVD
Liposarcoma	21253554	CNVD
Prostate cancer	19156837	CNVD
Emphysema	19352772	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Malignant germ cell tumour	17285132	CNVD
Melanoma	18172304	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Wilms tumour	21544195	CNVD
Squamous cell cancer	21044232	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	19960244	CNVD
Endometrial cancer	22040021	CNVD
Colorectal cancer	20709793	CNVD
Breast cancer	21264507	CNVD
Cancer	16751803	CNVD
Testicular cancer	18059402	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Seminomas	18059402	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
Testicular germ cell tumor	18059402	CNVD
Malaria	21533027	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Ewing''s sarcoma	17952124	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Breast cancer	21858162	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21785460	CNVD
Myelodysplastic syndrome	21251322	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Cancer	20164919	CNVD
Epilepsy	21858020	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Myelofibrosis	22110671	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
craniofacial dysmorphism	21918468	CNVD
Malignant peripheral nerve sheath tumor	19844265	CNVD
Chronic lymphocytic leukemia	21049055	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Alzheimer''s disease	17160897	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Breast cancer	21364760	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	17289997	CNVD
early-passage human iPS cells	21368824	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Schizophrenia	20967226	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:97 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:8333400-8379800	Weak transcription	Brain Substantia Nigra	brain
2	chr12:8333800-8352200	Weak transcription	Brain Hippocampus Middle	brain
3	chr12:8334200-8347600	Weak transcription	Brain Inferior Temporal Lobe	brain
4	chr12:8334200-8352400	Weak transcription	Fetal Stomach	stomach
5	chr12:8334600-8349000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
6	chr12:8335000-8350000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
7	chr12:8335200-8379800	Weak transcription	Brain Angular Gyrus	brain
8	chr12:8338800-8351200	Weak transcription	Brain Germinal Matrix	brain
9	chr12:8341600-8346800	Weak transcription	Brain Anterior Caudate	brain
10	chr12:8344000-8347200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
11	chr12:8345000-8352000	Weak transcription	Adipose Nuclei	Adipose
12	chr12:8345200-8347600	Weak transcription	Stomach Smooth Muscle	stomach
13	chr12:8345400-8349400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
14	chr12:8345600-8350000	Weak transcription	Primary B cells from peripheral blood	blood
15	chr12:8346600-8347000	Enhancers	Brain Cingulate Gyrus	brain
16	chr12:8346600-8349800	Weak transcription	Left Ventricle	heart
17	chr12:8346800-8347000	Enhancers	Brain Anterior Caudate	brain
18	chr12:8347000-8347600	Weak transcription	Brain Cingulate Gyrus	brain
19	chr12:8347000-8350800	Weak transcription	Cortex derived primary cultured neurospheres	brain
20	chr12:8347000-8379800	Weak transcription	Brain Anterior Caudate	brain
21	chr12:8347200-8348600	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
22	chr12:8347400-8350600	Weak transcription	Ovary	ovary
23	chr12:8347600-8348000	Strong transcription	Brain Cingulate Gyrus	brain
24	chr12:8347600-8348000	Strong transcription	Stomach Smooth Muscle	stomach
25	chr12:8347600-8349400	Strong transcription	Brain Inferior Temporal Lobe	brain
26	chr12:8347600-8350000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
27	chr12:8347600-8350800	Weak transcription	Colon Smooth Muscle	Colon
28	chr12:8348000-8349000	Weak transcription	Brain Cingulate Gyrus	brain
29	chr12:8348000-8349000	Weak transcription	Stomach Smooth Muscle	stomach
30	chr12:8348200-8359000	Weak transcription	Fetal Brain Female	brain
31	chr12:8348600-8351800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
32	chr12:8348800-8351800	Weak transcription	Aorta	Aorta
33	chr12:8349000-8349600	Strong transcription	Brain Dorsolateral Prefrontal Cortex	brain
34	chr12:8349000-8350600	Strong transcription	Brain Cingulate Gyrus	brain
35	chr12:8349000-8350600	Strong transcription	Stomach Smooth Muscle	stomach
36	chr12:8349400-8390000	Weak transcription	Brain Inferior Temporal Lobe	brain
37	chr12:8349600-8379600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
38	chr12:8350000-8350400	Enhancers	HSMM	muscle
39	chr12:8350000-8350400	Enhancers	HSMMtube	muscle
40	chr12:8350000-8350400	Enhancers	NHLF	lung
41	chr12:8350000-8350600	Strong transcription	Breast Myoepithelial Primary Cells	Breast
42	chr12:8350000-8351000	Enhancers	NHDF-Ad	bronchial
43	chr12:8350000-8351000	Enhancers	Osteobl	bone
44	chr12:8350000-8351200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
45	chr12:8350000-8351200	Enhancers	Skeletal Muscle Female	skeletal muscle
46	chr12:8350000-8351600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
47	chr12:8350200-8350600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
48	chr12:8350200-8350600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
49	chr12:8350200-8350600	Enhancers	Muscle Satellite Cultured Cells	--
50	chr12:8350200-8350600	Enhancers	NH-A	brain

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