Variant report

Variant	nsv1000696
Chromosome Location	chr2:12162843-12241022
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1436)
CpG islands
(count:306)
Chromatin interactive
region (count:27)
LncRNA
region (count:9)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1436 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:12214078-12214735	K562	blood:	n/a	n/a
2	ARID3A	chr2:12190510-12190853	K562	blood:	n/a	n/a
3	ARID3A	chr2:12215220-12215309	K562	blood:	n/a	n/a
4	ARID3A	chr2:12199810-12200006	K562	blood:	n/a	n/a
5	ARID3A	chr2:12224320-12224487	K562	blood:	n/a	n/a
6	ARID3A	chr2:12200260-12200798	K562	blood:	n/a	n/a
7	ATF1	chr2:12190507-12190860	K562	blood:	n/a	n/a
8	ATF1	chr2:12214190-12214878	K562	blood:	n/a	n/a
9	ATF1	chr2:12224211-12224502	K562	blood:	n/a	n/a
10	ATF2	chr2:12197329-12198127	GM12878	blood:	n/a	n/a
11	ATF2	chr2:12172549-12173049	GM12878	blood:	n/a	n/a
12	ATF2	chr2:12184828-12185404	GM12878	blood:	n/a	n/a
13	ATF2	chr2:12211397-12211889	GM12878	blood:	n/a	n/a
14	ATF2	chr2:12211462-12211854	GM12878	blood:	n/a	n/a
15	ATF2	chr2:12172424-12173014	GM12878	blood:	n/a	n/a
16	ATF2	chr2:12174320-12175009	GM12878	blood:	n/a	n/a
17	ATF2	chr2:12216889-12217266	GM12878	blood:	n/a	n/a
18	ATF2	chr2:12185775-12186473	GM12878	blood:	n/a	n/a
19	ATF2	chr2:12185827-12186453	GM12878	blood:	n/a	n/a
20	ATF2	chr2:12214201-12214689	GM12878	blood:	n/a	n/a
21	ATF3	chr2:12214161-12214796	K562	blood:	n/a	chr2:12214471-12214491
22	ATF3	chr2:12200022-12200450	K562	blood:	n/a	n/a
23	BACH1	chr2:12197730-12197944	H1-hESC	embryonic stem cell:	n/a	n/a
24	BATF	chr2:12190537-12190844	GM12878	blood:	n/a	n/a
25	BATF	chr2:12197554-12197870	GM12878	blood:	n/a	n/a
26	BATF	chr2:12185846-12186367	GM12878	blood:	n/a	n/a
27	BATF	chr2:12215793-12215994	GM12878	blood:	n/a	n/a
28	BATF	chr2:12185988-12186297	GM12878	blood:	n/a	n/a
29	BATF	chr2:12216963-12217290	GM12878	blood:	n/a	n/a
30	BATF	chr2:12172595-12172856	GM12878	blood:	n/a	n/a
31	BATF	chr2:12215757-12216021	GM12878	blood:	n/a	n/a
32	BATF	chr2:12214284-12214640	GM12878	blood:	n/a	chr2:12214480-12214493
33	BCL11A	chr2:12197592-12197896	GM12878	blood:	n/a	n/a
34	BCL11A	chr2:12185952-12186265	GM12878	blood:	n/a	n/a
35	BCL11A	chr2:12223232-12223426	H1-hESC	embryonic stem cell:	n/a	n/a
36	BCL11A	chr2:12197485-12197956	GM12878	blood:	n/a	chr2:12197932-12197941
37	BCL11A	chr2:12214363-12214649	GM12878	blood:	n/a	n/a
38	BCL11A	chr2:12214269-12214720	GM12878	blood:	n/a	chr2:12214307-12214314
39	BCL11A	chr2:12211508-12211807	GM12878	blood:	n/a	chr2:12211643-12211652
40	BCL11A	chr2:12211422-12211829	GM12878	blood:	n/a	chr2:12211643-12211652
41	BCL3	chr2:12237953-12238250	GM12878	blood:	n/a	n/a
42	BCL3	chr2:12228185-12228478	GM12878	blood:	n/a	n/a
43	BCL3	chr2:12197564-12197985	GM12878	blood:	n/a	chr2:12197932-12197941
44	BCLAF1	chr2:12184910-12185348	GM12878	blood:	n/a	n/a
45	BCLAF1	chr2:12214128-12214778	K562	blood:	n/a	chr2:12214307-12214314
46	BCLAF1	chr2:12172416-12173028	GM12878	blood:	n/a	n/a
47	BCLAF1	chr2:12190397-12190921	GM12878	blood:	n/a	n/a
48	BCLAF1	chr2:12197493-12198087	GM12878	blood:	n/a	chr2:12197932-12197941
49	BCLAF1	chr2:12185792-12186643	GM12878	blood:	n/a	n/a
50	BHLHE40	chr2:12214180-12214847	K562	blood:	n/a	n/a

(count:306 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:12237012-12237062	SKMC	muscle:	n/a
2	chr2:12237012-12237062	SKMC	muscle:	n/a
3	chr2:12163619-12163669	PrEC	prostate:	n/a
4	chr2:12237012-12237062	HUVEC	blood vessel:	n/a
5	chr2:12237012-12237062	CMK	blood:	n/a
6	chr2:12223636-12223686	HL-60	blood:	n/a
7	chr2:12163118-12163168	HRE	kidney:	n/a
8	chr2:12237012-12237062	SAEC	small airway:	n/a
9	chr2:12173618-12173668	SK-N-SH_RA	brain:	n/a
10	chr2:12223636-12223686	AG04450	lung:	fetal
11	chr2:12163118-12163168	PFSK-1	brain:	n/a
12	chr2:12163619-12163669	LNCaP	prostate:	n/a
13	chr2:12163619-12163669	GM12878	blood:	n/a
14	chr2:12163619-12163669	GM06990	blood:	n/a
15	chr2:12163118-12163168	AG10803	skin:	n/a
16	chr2:12163118-12163168	SK-N-SH	brain:	n/a
17	chr2:12237012-12237062	GM19239	blood:	n/a
18	chr2:12163619-12163669	MCF-7	breast:	n/a
19	chr2:12173618-12173668	ovcar-3	ovarian:	n/a
20	chr2:12173618-12173668	HMEC	breast:	n/a
21	chr2:12163118-12163168	CMK	blood:	n/a
22	chr2:12173618-12173668	HRPEpiC	eye:	n/a
23	chr2:12163118-12163168	U87	brain:	n/a
24	chr2:12173618-12173668	Hela-S3	cervix:	n/a
25	chr2:12163619-12163669	HEK293	kidney:	embryo
26	chr2:12163118-12163168	HCM	heart:	n/a
27	chr2:12237012-12237062	HCT-116	colon:	n/a
28	chr2:12163619-12163669	HUVEC	blood vessel:	n/a
29	chr2:12237012-12237062	PFSK-1	brain:	n/a
30	chr2:12223636-12223686	A549	lung:	n/a
31	chr2:12223636-12223686	Jurkat	blood:	n/a
32	chr2:12223636-12223686	PrEC	prostate:	n/a
33	chr2:12173618-12173668	U87	brain:	n/a
34	chr2:12173618-12173668	BJ	skin:	n/a
35	chr2:12173618-12173668	AG04449	skin:	fetal
36	chr2:12163619-12163669	SKMC	muscle:	n/a
37	chr2:12163619-12163669	SK-N-SH_RA	brain:	n/a
38	chr2:12223636-12223686	AG10803	skin:	n/a
39	chr2:12163619-12163669	ovcar-3	ovarian:	n/a
40	chr2:12173618-12173668	HCT-116	colon:	n/a
41	chr2:12223636-12223686	HPAEpiC	pulmonary alveolar:	n/a
42	chr2:12223636-12223686	AG04449	skin:	fetal
43	chr2:12173618-12173668	CMK	blood:	n/a
44	chr2:12237012-12237062	HNPCEpiC	eye:	n/a
45	chr2:12163619-12163669	U87	brain:	n/a
46	chr2:12237012-12237062	GM06990	blood:	n/a
47	chr2:12237012-12237062	HAEpiC	amniotic membrane:	n/a
48	chr2:12223636-12223686	GM12878	blood:	n/a
49	chr2:12237012-12237062	HRE	kidney:	n/a
50	chr2:12163619-12163669	T-47D	breast:	n/a

(count:27 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:12003510..12004337-chr2:12188494..12189188,2	MCF-7	breast:
2	chr2:12176844..12179370-chr2:12184810..12186635,2	MCF-7	breast:
3	chr2:12180693..12182626-chr2:12190865..12193405,2	K562	blood:
4	chr2:12225032..12227788-chr2:12236883..12238625,2	K562	blood:
5	chr2:12240589..12242524-chr2:12244995..12247436,2	K562	blood:
6	chr2:12222114..12225189-chr2:12227458..12230399,3	K562	blood:
7	chr2:12222114..12225189-chr2:12227458..12230399,3	K562	blood:
8	chr2:12228495..12230173-chr2:12235680..12237558,2	K562	blood:
9	chr2:12202416..12205140-chr2:12205945..12209401,3	K562	blood:
10	chr2:12219592..12223181-chr2:12244088..12246187,3	K562	blood:
11	chr2:12233977..12235737-chr2:12241751..12243264,2	K562	blood:
12	chr2:12200110..12202419-chr2:12206699..12209506,2	K562	blood:
13	chr2:12155340..12157815-chr2:12177536..12179462,2	MCF-7	breast:
14	chr2:12226565..12229995-chr2:12235703..12237819,3	K562	blood:
15	chr2:12142937..12145403-chr2:12173680..12175523,2	K562	blood:
16	chr2:12200110..12202419-chr2:12206699..12209506,2	K562	blood:
17	chr2:12180693..12182626-chr2:12190865..12193405,2	K562	blood:
18	chr2:12225032..12227788-chr2:12236883..12238625,2	K562	blood:
19	chr2:12222240..12225810-chr2:12227711..12231664,3	K562	blood:
20	chr2:12176844..12179370-chr2:12184810..12186635,2	MCF-7	breast:
21	chr2:12194778..12196811-chr2:12221641..12223390,2	K562	blood:
22	chr2:12228495..12230173-chr2:12235680..12237558,2	K562	blood:
23	chr2:12194778..12196811-chr2:12221641..12223390,2	K562	blood:
24	chr2:12202416..12205140-chr2:12205945..12209401,3	K562	blood:
25	chr2:12222240..12225810-chr2:12227711..12231664,3	K562	blood:
26	chr2:12226565..12229995-chr2:12235703..12237819,3	K562	blood:
27	chr2:12003714..12004353-chr2:12188666..12189311,2	MCF-7	breast:

(count:9 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GREB1-10	chr2:12188883-12189162	NONHSAT069209
2	lnc-LPIN1-1	chr2:12223575-12223744	ENSG00000224184
3	lnc-GREB1-10	chr2:12164161-12164261	NONHSAT069216
4	lnc-GREB1-10	chr2:12224315-12224432	NONHSAT069210
5	lnc-LPIN1-1	chr2:12223575-12223743	NR_110198
6	lnc-GREB1-10	chr2:12188883-12189125	NONHSAT069216
7	lnc-GREB1-10	chr2:12164395-12164528	NONHSAT069216
8	lnc-GREB1-10	chr2:12164395-12164528	NONHSAT069209
9	lnc-GREB1-10	chr2:12224315-12224432	NONHSAT069196

No data

Variant related genes	Relation type
ENSG00000238503	TF binding region
ENSG00000238503	CpG island
ENSG00000224184	chromatin interactions

Extended variants
information (count: 3079 )
Associated
traits (count: 69 )

Variant overlapped rSNPs/rCNVs (count:3079 , 50 per page) page: 1 2 3 4 5 6 7 ... 62

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs561108864	chr2:12162952-12162953	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
2	rs62113769	chr2:12162965-12162966	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs540503414	chr2:12162974-12162975	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
4	rs142922113	chr2:12162986-12162987	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
5	rs532400392	chr2:12162998-12162999	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
6	rs200666821	chr2:12163132-12163133	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs373604616	chr2:12163133-12163134	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs71394784	chr2:12163134-12163135	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs55701341	chr2:12163147-12163148	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs199535568	chr2:12163178-12163179	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs550905518	chr2:12163200-12163201	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs189099878	chr2:12163221-12163222	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs12692452	chr2:12163225-12163226	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
14	rs146160210	chr2:12163243-12163244	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs555638655	chr2:12163317-12163318	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs567448936	chr2:12163337-12163338	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs572151550	chr2:12163371-12163372	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs534851841	chr2:12163386-12163387	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs181766799	chr2:12163390-12163391	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs186583964	chr2:12163414-12163415	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs140196651	chr2:12163501-12163502	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs556873076	chr2:12163503-12163504	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs536359255	chr2:12163506-12163507	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs13026386	chr2:12163521-12163522	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs372802983	chr2:12163533-12163534	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs535914636	chr2:12163567-12163568	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs554270147	chr2:12163596-12163597	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs573085134	chr2:12163613-12163614	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs190989792	chr2:12163614-12163615	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs181010704	chr2:12163619-12163620	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs577426000	chr2:12163620-12163621	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs149848028	chr2:12163630-12163631	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs370418075	chr2:12163695-12163696	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs562872841	chr2:12163696-12163697	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs186424052	chr2:12163760-12163761	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs144915286	chr2:12163786-12163787	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs191067656	chr2:12163788-12163789	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs4669796	chr2:12163800-12163801	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs182561884	chr2:12163900-12163901	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs571360334	chr2:12163950-12163951	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs187215987	chr2:12163961-12163962	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs550620829	chr2:12164004-12164005	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs190688605	chr2:12164005-12164006	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs535877010	chr2:12164008-12164009	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs554233265	chr2:12164065-12164066	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs183209182	chr2:12164077-12164078	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs200690085	chr2:12164085-12164086	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs13027180	chr2:12164105-12164106	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs116810853	chr2:12164120-12164121	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs188921371	chr2:12164126-12164127	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:69)

Disease	PMID	Source
Breast cancer	17133270	CNVD
Mental retardation	17847001	CNVD
Glioblastoma multiforme	21080181	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Cancer	20164920	CNVD
Neuroblastoma	21508638	CNVD
Breast cancer	17603634	CNVD
Cancer	16751803	CNVD
Neuroblastoma	16790693	CNVD
Colorectal cancer	16272173	CNVD
Breast cancer	17393978	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Medulloblastoma	21979893	CNVD
Lynch syndrome	18415027	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17387387	CNVD
Neuroblastoma	17533364	CNVD
Neuroblastoma	18923191	CNVD
Endometrial cancer	22040021	CNVD
Adrenal tumor	17535989	CNVD
Breast cancer	21264507	CNVD
Basal cell lymphoma	17053054	CNVD
Medulloblastoma	17522785	CNVD
Cancer	23418310	CNVD
Ewing''s sarcoma	21437220	CNVD
Ependymoma	16718352	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
lymphocytic leukemia	21291569	CNVD
Prostate cancer	18632612	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Bladder cancer	21909424	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Cancer	20164919	CNVD
Hodgkin''s lymphoma	18641027	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Breast cancer	21364760	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Follicular lymphoma	20505157	CNVD
Autism	17483303	CNVD
Breast cancer	21804112	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	22286061	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Glioma	17123091	CNVD
Breast cancer	20409316	CNVD
Multiple myeloma	16616336	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	21785460	CNVD
Medulloblastoma	20607354	CNVD
Acute myeloid leukemia	20729466	CNVD
Medulloblastoma	19270706	CNVD
Prostate cancer	19258504	CNVD
Neuroblastoma	19638189	CNVD
Neuroblastoma	19435921	CNVD
Neuroblastoma	18574593	CNVD
Acute myeloid leukemia	18000384	CNVD
Medulloblastoma	16968546	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:974 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:12155000-12164000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
2	chr2:12157800-12163000	ZNF genes & repeats	GM12878-XiMat	blood
3	chr2:12162600-12164000	Enhancers	Breast Myoepithelial Primary Cells	Breast
4	chr2:12162800-12163600	Weak transcription	HUES64 Cell Line	embryonic stem cell
5	chr2:12163400-12164600	Enhancers	NHDF-Ad	bronchial
6	chr2:12163600-12164400	Enhancers	Fetal Heart	heart
7	chr2:12163600-12164600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
8	chr2:12163600-12165000	Enhancers	HSMM	muscle
9	chr2:12163600-12165000	Enhancers	HSMMtube	muscle
10	chr2:12163800-12164600	Enhancers	HMEC	breast
11	chr2:12163800-12165000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
12	chr2:12163800-12165000	Enhancers	Osteobl	bone
13	chr2:12164000-12165000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
14	chr2:12164000-12165000	Enhancers	Muscle Satellite Cultured Cells	--
15	chr2:12164000-12165000	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
16	chr2:12164200-12164600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
17	chr2:12164200-12164600	Enhancers	Colon Smooth Muscle	Colon
18	chr2:12164200-12165000	Enhancers	NH-A	brain
19	chr2:12165800-12166400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
20	chr2:12166200-12166600	Enhancers	HUES64 Cell Line	embryonic stem cell
21	chr2:12167400-12167600	Enhancers	K562	blood
22	chr2:12167600-12171800	Weak transcription	K562	blood
23	chr2:12167600-12172400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
24	chr2:12171200-12171400	Enhancers	Stomach Mucosa	stomach
25	chr2:12171200-12172400	Enhancers	Primary B cells from cord blood	blood
26	chr2:12171200-12178000	Enhancers	Primary B cells from peripheral blood	blood
27	chr2:12171400-12171600	Enhancers	GM12878-XiMat	blood
28	chr2:12171400-12171800	Flanking Active TSS	Stomach Mucosa	stomach
29	chr2:12171400-12173600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
30	chr2:12171600-12172400	Enhancers	Gastric	stomach
31	chr2:12171600-12172800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
32	chr2:12171600-12173400	Flanking Active TSS	GM12878-XiMat	blood
33	chr2:12171800-12172400	Enhancers	Fetal Heart	heart
34	chr2:12171800-12172400	Enhancers	Stomach Mucosa	stomach
35	chr2:12171800-12172400	Enhancers	K562	blood
36	chr2:12172000-12172400	Enhancers	Brain Cingulate Gyrus	brain
37	chr2:12172000-12172400	Bivalent Enhancer	Fetal Brain Male	brain
38	chr2:12172000-12172400	Enhancers	Left Ventricle	heart
39	chr2:12172000-12173400	Enhancers	Cortex derived primary cultured neurospheres	brain
40	chr2:12172200-12172400	Enhancers	Fetal Muscle Trunk	muscle
41	chr2:12172200-12172800	Enhancers	Ovary	ovary
42	chr2:12172200-12174000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
43	chr2:12172200-12174000	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
44	chr2:12172200-12174200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
45	chr2:12172200-12176000	Enhancers	Breast Myoepithelial Primary Cells	Breast
46	chr2:12172400-12172600	Flanking Active TSS	Primary B cells from cord blood	blood
47	chr2:12172400-12173000	Enhancers	ES-I3 Cell Line	embryonic stem cell
48	chr2:12172400-12173800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
49	chr2:12172400-12174400	Weak transcription	Fetal Muscle Trunk	muscle
50	chr2:12172400-12175800	Weak transcription	K562	blood

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