Variant report

Variant	nsv898756
Chromosome Location	chr12:10142538-10174314
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	BACH1	chr12:10169475-10169842	H1-hESC	embryonic stem cell:	n/a	n/a
2	CEBPB	chr12:10169328-10169471	HepG2	liver:	n/a	chr12:10169399-10169410
3	CEBPB	chr12:10153919-10154049	H1-hESC	embryonic stem cell:	n/a	n/a
4	CHD1	chr12:10163016-10163077	GM12878	blood:	n/a	n/a
5	CTCF	chr12:10162580-10162730	AoAF	blood vessel:	n/a	chr12:10162666-10162687 chr12:10162667-10162680 chr12:10162665-10162681 chr12:10162664-10162682
6	CTCF	chr12:10162580-10162730	HCPEpiC	choroid plexus:	n/a	chr12:10162666-10162687 chr12:10162667-10162680 chr12:10162665-10162681 chr12:10162664-10162682
7	CTCF	chr12:10162600-10162750	AG10803	skin:	n/a	chr12:10162666-10162687 chr12:10162667-10162680 chr12:10162665-10162681 chr12:10162664-10162682
8	CTCF	chr12:10162600-10162750	HCPEpiC	choroid plexus:	n/a	chr12:10162666-10162687 chr12:10162667-10162680 chr12:10162665-10162681 chr12:10162664-10162682
9	CTCF	chr12:10162580-10162730	GM12875	blood:	n/a	chr12:10162666-10162687 chr12:10162667-10162680 chr12:10162665-10162681 chr12:10162664-10162682
10	CTCF	chr12:10150957-10151045	Kidney_OC	kidney:	n/a	n/a
11	CTCF	chr12:10162580-10162730	SK-N-SH_RA	brain:	n/a	chr12:10162666-10162687 chr12:10162667-10162680 chr12:10162665-10162681 chr12:10162664-10162682
12	CTCF	chr12:10162240-10162390	AoAF	blood vessel:	n/a	n/a
13	CTCF	chr12:10162520-10162670	GM12869	blood:	n/a	n/a
14	CTCF	chr12:10162576-10162767	Lung_OC	lung:	n/a	chr12:10162666-10162687 chr12:10162667-10162680 chr12:10162665-10162681 chr12:10162664-10162682
15	CTCF	chr12:10162544-10162786	GM12878	blood:	n/a	chr12:10162666-10162687 chr12:10162667-10162680 chr12:10162665-10162681 chr12:10162664-10162682
16	CTCF	chr12:10158333-10158370	GM12878	blood:	n/a	n/a
17	CTCF	chr12:10162600-10162750	RPTEC	kidney:	n/a	chr12:10162666-10162687 chr12:10162667-10162680 chr12:10162665-10162681 chr12:10162664-10162682
18	CTCF	chr12:10150917-10151039	GM12892	blood:	n/a	n/a
19	CTCF	chr12:10162565-10162792	MCF-7	breast:	n/a	chr12:10162666-10162687 chr12:10162667-10162680 chr12:10162665-10162681 chr12:10162664-10162682
20	CTCF	chr12:10162960-10163110	HRE	kidney:	n/a	n/a
21	CTCF	chr12:10162580-10162730	SAEC	small airway:	n/a	chr12:10162666-10162687 chr12:10162667-10162680 chr12:10162665-10162681 chr12:10162664-10162682
22	CTCF	chr12:10156980-10157130	HEK293	kidney:	n/a	n/a
23	CTCF	chr12:10162280-10162430	HAc	cerebellar:	n/a	n/a
24	CTCF	chr12:10162600-10162750	GM12872	blood:	n/a	chr12:10162666-10162687 chr12:10162667-10162680 chr12:10162665-10162681 chr12:10162664-10162682
25	CTCF	chr12:10162600-10162750	GM12864	blood:	n/a	chr12:10162666-10162687 chr12:10162667-10162680 chr12:10162665-10162681 chr12:10162664-10162682
26	CTCF	chr12:10162235-10162373	Hela-S3	cervix:	n/a	n/a
27	CTCF	chr12:10162140-10162290	GM12873	blood:	n/a	n/a
28	CTCF	chr12:10150935-10151031	MCF-7	breast:	n/a	n/a
29	CTCF	chr12:10162564-10162787	NHEK	skin:	n/a	chr12:10162666-10162687 chr12:10162667-10162680 chr12:10162665-10162681 chr12:10162664-10162682
30	CTCF	chr12:10150912-10151036	MCF-7	breast:	n/a	n/a
31	CTCF	chr12:10162260-10162410	GM12872	blood:	n/a	n/a
32	CTCF	chr12:10162580-10162730	HRE	kidney:	n/a	chr12:10162666-10162687 chr12:10162667-10162680 chr12:10162665-10162681 chr12:10162664-10162682
33	CTCF	chr12:10162200-10162350	GM12865	blood:	n/a	n/a
34	CTCF	chr12:10162537-10162821	Hela-S3	cervix:	n/a	chr12:10162666-10162687 chr12:10162667-10162680 chr12:10162665-10162681 chr12:10162664-10162682
35	CTCF	chr12:10162600-10162750	HEEpiC	esophagus:	n/a	chr12:10162666-10162687 chr12:10162667-10162680 chr12:10162665-10162681 chr12:10162664-10162682
36	CTCF	chr12:10162527-10162801	HUVEC	blood vessel:	n/a	chr12:10162666-10162687 chr12:10162667-10162680 chr12:10162665-10162681 chr12:10162664-10162682
37	CTCF	chr12:10162140-10162290	GM12866	blood:	n/a	n/a
38	CTCF	chr12:10162584-10162753	Pancreas_OC	pancreas:	n/a	chr12:10162666-10162687 chr12:10162667-10162680 chr12:10162665-10162681 chr12:10162664-10162682
39	CTCF	chr12:10162632-10162714	GM12892	blood:	n/a	chr12:10162666-10162687 chr12:10162667-10162680 chr12:10162665-10162681 chr12:10162664-10162682
40	CTCF	chr12:10162820-10162970	HFF-Myc	foreskin:	n/a	n/a
41	CTCF	chr12:10162580-10162725	Kidney_OC	kidney:	n/a	chr12:10162666-10162687 chr12:10162667-10162680 chr12:10162665-10162681 chr12:10162664-10162682
42	CTCF	chr12:10150942-10151028	GM12878	blood:	n/a	n/a
43	CTCF	chr12:10162550-10162779	ProgFib	skin:	n/a	chr12:10162666-10162687 chr12:10162667-10162680 chr12:10162665-10162681 chr12:10162664-10162682
44	CTCF	chr12:10162376-10162894	HCT-116	colon:	n/a	chr12:10162666-10162687 chr12:10162667-10162680 chr12:10162665-10162681 chr12:10162664-10162682
45	CTCF	chr12:10162440-10162590	NHEK	skin:	n/a	n/a
46	CTCF	chr12:10162582-10162726	SK-N-SH_RA	brain:	n/a	chr12:10162666-10162687 chr12:10162667-10162680 chr12:10162665-10162681 chr12:10162664-10162682
47	CTCF	chr12:10150938-10151046	GM19238	blood:	n/a	n/a
48	CTCF	chr12:10163040-10163190	HepG2	liver:	n/a	n/a
49	CTCF	chr12:10150931-10150933	A549	lung:	n/a	n/a
50	CTCF	chr12:10162600-10162750	HRE	kidney:	n/a	chr12:10162666-10162687 chr12:10162667-10162680 chr12:10162665-10162681 chr12:10162664-10162682

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:10153316-10153366	HRCEpiC	kidney:	n/a
2	chr12:10163030-10163080	GM06990	blood:	n/a
3	chr12:10153316-10153366	HRCEpiC	kidney:	n/a
4	chr12:10163030-10163080	GM06990	blood:	n/a
5	chr12:10171151-10171201	A549	lung:	n/a
6	chr12:10162301-10162351	A549	lung:	n/a
7	chr12:10163345-10163395	GM06990	blood:	n/a
8	chr12:10161687-10161737	HCF	heart:	n/a
9	chr12:10150905-10150955	HCM	heart:	n/a
10	chr12:10162301-10162351	SKMC	muscle:	n/a
11	chr12:10163030-10163080	SKMC	muscle:	n/a
12	chr12:10151707-10151757	GM19239	blood:	n/a
13	chr12:10163030-10163080	GM19239	blood:	n/a
14	chr12:10150905-10150955	SKMC	muscle:	n/a
15	chr12:10163345-10163395	HEEpiC	esophagus:	n/a
16	chr12:10151707-10151757	HCPEpiC	choroid plexus:	n/a
17	chr12:10162301-10162351	Jurkat	blood:	n/a
18	chr12:10161687-10161737	Jurkat	blood:	n/a
19	chr12:10163345-10163395	CMK	blood:	n/a
20	chr12:10161757-10161807	NT2-D1	testis:	n/a
21	chr12:10171151-10171201	Hela-S3	cervix:	n/a
22	chr12:10161757-10161807	LNCaP	prostate:	n/a
23	chr12:10151707-10151757	AG04449	skin:	fetal
24	chr12:10150905-10150955	PANC-1	pancreas:	n/a
25	chr12:10161757-10161807	PrEC	prostate:	n/a
26	chr12:10151707-10151757	SAEC	small airway:	n/a
27	chr12:10163345-10163395	NHBE	bronchial:	n/a
28	chr12:10153316-10153366	ECC-1	luminal epithelium:	n/a
29	chr12:10151707-10151757	HL-60	blood:	n/a
30	chr12:10163030-10163080	HCM	heart:	n/a
31	chr12:10171151-10171201	RPTEC	kidney:	n/a
32	chr12:10163532-10163582	NH-A	brain:	n/a
33	chr12:10163030-10163080	NB4	blood:	n/a
34	chr12:10150905-10150955	HCT-116	colon:	n/a
35	chr12:10161687-10161737	IMR90	lung:	fetal
36	chr12:10150905-10150955	PFSK-1	brain:	n/a
37	chr12:10163532-10163582	NHDF-neo	bronchial:	n/a
38	chr12:10150905-10150955	NH-A	brain:	n/a
39	chr12:10163030-10163080	ECC-1	luminal epithelium:	n/a
40	chr12:10151707-10151757	Hela-S3	cervix:	n/a
41	chr12:10153316-10153366	CMK	blood:	n/a
42	chr12:10171151-10171201	Jurkat	blood:	n/a
43	chr12:10150905-10150955	Jurkat	blood:	n/a
44	chr12:10163030-10163080	ovcar-3	ovarian:	n/a
45	chr12:10163030-10163080	NHDF-neo	bronchial:	n/a
46	chr12:10171151-10171201	ovcar-3	ovarian:	n/a
47	chr12:10161757-10161807	SK-N-SH	brain:	n/a
48	chr12:10171151-10171201	HCT-116	colon:	n/a
49	chr12:10171151-10171201	PrEC	prostate:	n/a
50	chr12:10151707-10151757	HCF	heart:	n/a

No.	Distal block	Cell Line	Cell type
1	chr12:9910779..9913756-chr12:10153448..10156029,2	K562	blood:
2	chr12:10166772..10168888-chr12:10170728..10172958,2	K562	blood:
3	chr12:10166772..10168888-chr12:10170728..10172958,2	K562	blood:
4	chr12:9966874..9967473-chr12:10162556..10163093,2	MCF-7	breast:
5	chr12:10171288..10174631-chr12:10176467..10178782,3	K562	blood:
6	chr12:10162252..10163209-chr12:10292996..10293711,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CLEC1B-1	chr12:10167839-10168372	ENSG00000256803.1
2	lnc-CLEC9A-2	chr12:10163358-10163449	NONHSAT026859
3	lnc-CLEC9A-2	chr12:10165384-10165822	NONHSAT026859
4	lnc-CLEC12B-1	chr12:10147617-10148293	NONHSAT026857

Variant related genes	Relation type
CLEC1B	TF binding region
CLEC12B	TF binding region
CLEC1B	CpG island
CLEC12B	CpG island
ENSG00000110848	chromatin interactions

Extended variants
information (count: 1370 )
Associated
traits (count: 87 )

Variant overlapped rSNPs/rCNVs (count:1370 , 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	rs678208	chr12:10142538-10142539	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs568376701	chr12:10142560-10142561	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs549952443	chr12:10142672-10142673	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs147052400	chr12:10142681-10142682	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs118132954	chr12:10142715-10142716	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs577106020	chr12:10142737-10142738	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs117030474	chr12:10142784-10142785	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs77402784	chr12:10142826-10142827	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs74766295	chr12:10142837-10142838	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs538651877	chr12:10142859-10142860	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs61917157	chr12:10142892-10142893	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs679982	chr12:10142897-10142898	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
13	rs147668713	chr12:10142920-10142921	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs76024376	chr12:10142942-10142943	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs374770211	chr12:10142950-10142951	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs74061448	chr12:10142956-10142957	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs563886685	chr12:10142957-10142958	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs532558893	chr12:10142979-10142980	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs552380477	chr12:10143000-10143001	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs368360602	chr12:10143022-10143023	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs191361944	chr12:10143097-10143098	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs367604601	chr12:10143101-10143102	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs559209129	chr12:10143122-10143123	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs528725269	chr12:10143126-10143127	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs548610419	chr12:10143131-10143132	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs568393885	chr12:10143138-10143139	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs537095252	chr12:10143236-10143237	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs551042230	chr12:10143296-10143297	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs142328869	chr12:10143321-10143322	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs146908009	chr12:10143333-10143334	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs553177377	chr12:10143349-10143350	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs573092513	chr12:10143350-10143351	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs535701203	chr12:10143388-10143389	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs555378308	chr12:10143403-10143404	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs575173544	chr12:10143412-10143413	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs1359081	chr12:10143498-10143499	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
37	rs563815522	chr12:10143514-10143515	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs115616284	chr12:10143517-10143518	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs369906217	chr12:10143537-10143538	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs35985272	chr12:10143545-10143546	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs568414935	chr12:10143563-10143564	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs117684071	chr12:10143581-10143582	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs74688084	chr12:10143600-10143601	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs528679814	chr12:10143618-10143619	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs577411172	chr12:10143651-10143652	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs148372181	chr12:10143652-10143653	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs373760092	chr12:10143672-10143673	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs562282445	chr12:10143707-10143708	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs530916183	chr12:10143742-10143743	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs184119455	chr12:10143788-10143789	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:87)

Disease	PMID	Source
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
Acute lymphoblastic leukemia	22237106	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Breast cancer	21364760	CNVD
Breast cancer	21509527	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	21611746	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Myelofibrosis	22110671	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Squamous cell cancer	19607727	CNVD
Prostate cancer	16573809	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Glioblastoma multiforme	22286061	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Acute myeloid leukemia	17268525	CNVD
Acute monocytic leukemia	16498392	CNVD
Prostate cancer	16461572	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Breast cancer	17133270	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Ovarian cancer	21781307	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:179 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:10129200-10144400	Weak transcription	Primary hematopoietic stem cells	blood
2	chr12:10135800-10144600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
3	chr12:10138800-10142600	Weak transcription	HUES48 Cell Line	embryonic stem cell
4	chr12:10139400-10143400	Weak transcription	Monocytes-CD14+_RO01746	blood
5	chr12:10140200-10143400	Weak transcription	Primary monocytes fromperipheralblood	blood
6	chr12:10140800-10144400	Weak transcription	Primary neutrophils fromperipheralblood	blood
7	chr12:10142600-10143200	Enhancers	HUES48 Cell Line	embryonic stem cell
8	chr12:10143400-10143600	Enhancers	Primary monocytes fromperipheralblood	blood
9	chr12:10143400-10144200	Enhancers	Monocytes-CD14+_RO01746	blood
10	chr12:10143600-10144000	Weak transcription	Primary monocytes fromperipheralblood	blood
11	chr12:10144000-10145200	Enhancers	Primary monocytes fromperipheralblood	blood
12	chr12:10144200-10144400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
13	chr12:10144200-10144600	Enhancers	Brain Anterior Caudate	brain
14	chr12:10144200-10144800	Bivalent Enhancer	Primary B cells from cord blood	blood
15	chr12:10144200-10145000	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
16	chr12:10144400-10144600	Enhancers	Brain Hippocampus Middle	brain
17	chr12:10144400-10144600	Enhancers	Brain Inferior Temporal Lobe	brain
18	chr12:10144400-10144800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
19	chr12:10144400-10145000	Enhancers	Primary hematopoietic stem cells short term culture	blood
20	chr12:10144400-10145600	Enhancers	Primary hematopoietic stem cells	blood
21	chr12:10144400-10145800	Enhancers	Primary neutrophils fromperipheralblood	blood
22	chr12:10144400-10145800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
23	chr12:10144600-10144800	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
24	chr12:10144600-10144800	Flanking Active TSS	Brain Hippocampus Middle	brain
25	chr12:10144600-10145000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
26	chr12:10144600-10145000	Enhancers	Brain Angular Gyrus	brain
27	chr12:10144600-10145000	Active TSS	Brain Inferior Temporal Lobe	brain
28	chr12:10144800-10145200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
29	chr12:10144800-10145200	Active TSS	Brain Anterior Caudate	brain
30	chr12:10144800-10145200	Active TSS	Brain Hippocampus Middle	brain
31	chr12:10144800-10146000	Enhancers	Primary B cells from cord blood	blood
32	chr12:10145000-10145200	Bivalent Enhancer	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
33	chr12:10145000-10145200	Active TSS	Monocytes-CD14+_RO01746	blood
34	chr12:10145000-10146000	Weak transcription	Brain Angular Gyrus	brain
35	chr12:10145200-10146200	Enhancers	Brain Hippocampus Middle	brain
36	chr12:10145200-10155400	Weak transcription	Monocytes-CD14+_RO01746	blood
37	chr12:10145200-10155800	Weak transcription	Primary monocytes fromperipheralblood	blood
38	chr12:10145800-10153400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
39	chr12:10146000-10146400	Enhancers	Brain Angular Gyrus	brain
40	chr12:10146000-10146400	Enhancers	Brain Substantia Nigra	brain
41	chr12:10149400-10149800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
42	chr12:10149400-10150000	Enhancers	Placenta Amnion	Placenta Amnion
43	chr12:10149800-10153400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
44	chr12:10150000-10153200	Weak transcription	Placenta Amnion	Placenta Amnion
45	chr12:10150800-10151800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
46	chr12:10151800-10152000	Enhancers	Primary hematopoietic stem cells short term culture	blood
47	chr12:10152000-10153800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
48	chr12:10153200-10154400	Enhancers	Placenta Amnion	Placenta Amnion
49	chr12:10153400-10154000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
50	chr12:10153400-10154000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin

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