Variant report

Variant	nsv1043314
Chromosome Location	chr12:341084-387718
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:284)
CpG islands
(count:793)
Chromatin interactive
region (count:12)
LncRNA
region (count:7)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:284 , 50 per page) page: 1 2 3 4 5 6

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr12:346692-346907	HepG2	liver:	n/a	n/a
2	ARID3A	chr12:345774-345842	HepG2	liver:	n/a	n/a
3	ATF1	chr12:373538-373815	K562	blood:	n/a	n/a
4	BATF	chr12:382502-382775	GM12878	blood:	n/a	n/a
5	BCL11A	chr12:368058-368307	GM12878	blood:	n/a	n/a
6	BCL3	chr12:377133-378098	A549	lung:	n/a	n/a
7	BHLHE40	chr12:344171-344359	K562	blood:	n/a	chr12:344223-344232 chr12:344217-344238 chr12:344223-344232 chr12:344222-344231 chr12:344221-344234
8	BHLHE40	chr12:346383-346899	HepG2	liver:	n/a	n/a
9	BHLHE40	chr12:366144-366293	K562	blood:	n/a	n/a
10	CBX3	chr12:344865-345227	K562	blood:	n/a	n/a
11	CEBPB	chr12:346655-346961	HepG2	liver:	n/a	n/a
12	CEBPB	chr12:362727-362918	HepG2	liver:	n/a	n/a
13	CEBPB	chr12:362659-363007	HepG2	liver:	n/a	n/a
14	CEBPB	chr12:373496-373744	K562	blood:	n/a	n/a
15	CHD2	chr12:346253-346254	HepG2	liver:	n/a	n/a
16	CHD2	chr12:346626-346894	HepG2	liver:	n/a	chr12:346769-346779
17	CTCF	chr12:348235-348288	Kidney_OC	kidney:	n/a	n/a
18	CTCF	chr12:363300-363450	HRPEpiC	eye:	n/a	n/a
19	CTCF	chr12:363373-363500	K562	blood:	n/a	n/a
20	CTCF	chr12:341540-341690	GM12864	blood:	n/a	n/a
21	CTCF	chr12:346145-346158	Kidney_OC	kidney:	n/a	n/a
22	CTCF	chr12:363372-363472	H1-hESC	embryonic stem cell:	n/a	n/a
23	CTCF	chr12:363380-363530	BE2_C	brain:	n/a	n/a
24	CTCF	chr12:363160-363310	GM12869	blood:	n/a	n/a
25	CTCF	chr12:345164-345259	Kidney_OC	kidney:	n/a	n/a
26	CTCF	chr12:363360-363510	HRPEpiC	eye:	n/a	n/a
27	CTCF	chr12:346355-346397	HepG2	liver:	n/a	n/a
28	CTCF	chr12:350333-350422	GM13976	blood:	n/a	n/a
29	CTCF	chr12:363438-363472	Kidney_OC	kidney:	n/a	n/a
30	CTCF	chr12:363426-363463	Hela-S3	cervix:	n/a	n/a
31	CTCF	chr12:361029-361079	GM10266	blood:	n/a	n/a
32	CTCF	chr12:363283-363609	K562	blood:	n/a	n/a
33	CTCF	chr12:376720-376870	SAEC	small airway:	n/a	n/a
34	CTCF	chr12:346700-346850	HepG2	liver:	n/a	chr12:346806-346819
35	CTCF	chr12:363360-363510	HepG2	liver:	n/a	n/a
36	CTCF	chr12:382320-382470	HCPEpiC	choroid plexus:	n/a	n/a
37	CTCF	chr12:363280-363430	Hela-S3	cervix:	n/a	n/a
38	CTCF	chr12:346320-346470	HepG2	liver:	n/a	n/a
39	CUX1	chr12:366305-366323	K562	blood:	n/a	n/a
40	CUX1	chr12:373538-373615	K562	blood:	n/a	n/a
41	EGR1	chr12:366155-366451	K562	blood:	n/a	chr12:366303-366314 chr12:366302-366315 chr12:366303-366314 chr12:366301-366316 chr12:366304-366314 chr12:366298-366320 chr12:366302-366316 chr12:366304-366314
42	EGR1	chr12:366140-366512	K562	blood:	n/a	chr12:366303-366314 chr12:366302-366315 chr12:366303-366314 chr12:366301-366316 chr12:366304-366314 chr12:366298-366320 chr12:366302-366316 chr12:366304-366314
43	ELF1	chr12:346647-346991	HepG2	liver:	n/a	chr12:346812-346823
44	ELF1	chr12:346651-347037	HepG2	liver:	n/a	chr12:346812-346823
45	EP300	chr12:346630-346941	HepG2	liver:	n/a	chr12:346814-346823
46	EP300	chr12:366111-366414	K562	blood:	n/a	chr12:366365-366379
47	EP300	chr12:346035-347065	HepG2	liver:	n/a	chr12:346814-346823
48	EP300	chr12:373428-374103	K562	blood:	n/a	n/a
49	EP300	chr12:346163-346872	HepG2	liver:	n/a	chr12:346814-346823
50	ESR1	chr12:372002-372346	ECC-1	luminal epithelium:	n/a	n/a

(count:793 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:371950-372000	HRCEpiC	kidney:	n/a
2	chr12:372049-372099	Caco-2	colon:	n/a
3	chr12:351361-351411	NHBE	bronchial:	n/a
4	chr12:351299-351349	SK-N-SH_RA	brain:	n/a
5	chr12:372246-372296	SK-N-MC	brain:	n/a
6	chr12:372049-372099	ovcar-3	ovarian:	n/a
7	chr12:372246-372296	HUVEC	blood vessel:	n/a
8	chr12:351299-351349	Jurkat	blood:	n/a
9	chr12:371916-371966	PANC-1	pancreas:	n/a
10	chr12:372049-372099	H1-hESC	embryonic stem cell:	embryo
11	chr12:341431-341481	ProgFib	skin:	n/a
12	chr12:372049-372099	LNCaP	prostate:	n/a
13	chr12:371916-371966	AG10803	skin:	n/a
14	chr12:378771-378821	SAEC	small airway:	n/a
15	chr12:371950-372000	PrEC	prostate:	n/a
16	chr12:372139-372189	Hepatocyte	liver:	n/a
17	chr12:378771-378821	NHBE	bronchial:	n/a
18	chr12:371950-372000	IMR90	lung:	fetal
19	chr12:371916-371966	NH-A	brain:	n/a
20	chr12:341431-341481	HCF	heart:	n/a
21	chr12:378771-378821	Jurkat	blood:	n/a
22	chr12:341431-341481	IMR90	lung:	fetal
23	chr12:371916-371966	PFSK-1	brain:	n/a
24	chr12:372191-372241	RPTEC	kidney:	n/a
25	chr12:372139-372189	HepG2	liver:	n/a
26	chr12:371916-371966	CMK	blood:	n/a
27	chr12:372139-372189	Hela-S3	cervix:	n/a
28	chr12:351361-351411	H1-hESC	embryonic stem cell:	embryo
29	chr12:371950-372000	AoSMC	blood vessel:	n/a
30	chr12:351262-351312	AoSMC	blood vessel:	n/a
31	chr12:372139-372189	HL-60	blood:	n/a
32	chr12:372246-372296	NHDF-neo	bronchial:	n/a
33	chr12:372049-372099	AG04450	lung:	fetal
34	chr12:372049-372099	NHBE	bronchial:	n/a
35	chr12:372246-372296	RPTEC	kidney:	n/a
36	chr12:372246-372296	HMEC	breast:	n/a
37	chr12:351299-351349	SK-N-MC	brain:	n/a
38	chr12:372246-372296	PrEC	prostate:	n/a
39	chr12:378771-378821	HIPEpiC	eye:	n/a
40	chr12:371916-371966	NT2-D1	testis:	n/a
41	chr12:372790-372840	HUVEC	blood vessel:	n/a
42	chr12:372191-372241	NHBE	bronchial:	n/a
43	chr12:351299-351349	HUVEC	blood vessel:	n/a
44	chr12:351262-351312	HMEC	breast:	n/a
45	chr12:371950-372000	HCM	heart:	n/a
46	chr12:372191-372241	K562	blood:	n/a
47	chr12:372049-372099	SK-N-MC	brain:	n/a
48	chr12:372049-372099	CMK	blood:	n/a
49	chr12:378771-378821	PFSK-1	brain:	n/a
50	chr12:371950-372000	HEK293	kidney:	embryo

(count:12 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:381899..385111-chr12:386819..388918,3	K562	blood:
2	chr12:371815..374343-chr12:375834..377592,4	K562	blood:
3	chr12:371815..373339-chr12:375834..377443,2	K562	blood:
4	chr12:335174..337021-chr12:347324..348997,2	MCF-7	breast:
5	chr12:381899..384416-chr12:386819..388918,2	K562	blood:
6	chr12:343024..345718-chr12:346456..348624,2	MCF-7	breast:
7	chr12:381899..385111-chr12:386819..388918,3	K562	blood:
8	chr12:378409..380462-chr12:383368..386178,2	MCF-7	breast:
9	chr12:371632..373367-chr12:383696..385601,2	MCF-7	breast:
10	chr12:381899..384416-chr12:386819..388918,2	K562	blood:
11	chr12:360330..361839-chr12:364810..367065,2	K562	blood:
12	chr12:378409..380462-chr12:383368..386178,2	MCF-7	breast:

(count:7 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-KDM5A-2	chr12:366437-366602	NONHSAT025324
2	lnc-KDM5A-2	chr12:365683-365806	NONHSAT025324
3	lnc-KDM5A-1	chr12:383120-386289	ENSG00000261799.1
4	lnc-KDM5A-2	chr12:362608-362913	ENSG00000255746.1
5	lnc-KDM5A-2	chr12:367087-367167	NONHSAT025324
6	lnc-KDM5A-2	chr12:366437-366465	ENSG00000255746.1
7	lnc-KDM5A-2	chr12:365639-365806	ENSG00000255746.1

No data

Variant related genes	Relation type
ENSG00000255746	TF binding region
SLC6A13	TF binding region
ENSG00000261799	TF binding region
ENSG00000255746	CpG island
SLC6A13	CpG island
ENSG00000261799	CpG island
ENSG00000010379	chromatin interactions
ENSG00000255746	chromatin interactions

Extended variants
information (count: 2041 )
Associated
traits (count: 84 )

Variant overlapped rSNPs/rCNVs (count:2041 , 50 per page) page: 1 2 3 4 5 6 7 ... 41

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs541476769	chr12:341088-341089	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs141531568	chr12:341123-341124	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs147018295	chr12:341127-341128	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs488192	chr12:341156-341157	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	mRNA abundance
5	rs147641026	chr12:341157-341158	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs528275486	chr12:341223-341224	Weak transcription Enhancers Bivalent Enhancer Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs186521196	chr12:341228-341229	Weak transcription Enhancers Bivalent Enhancer Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs546363636	chr12:341237-341238	Weak transcription Enhancers Bivalent Enhancer Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs565855248	chr12:341241-341242	Weak transcription Enhancers Bivalent Enhancer Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs142212024	chr12:341258-341259	Weak transcription Enhancers Bivalent Enhancer Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs537891055	chr12:341266-341267	Weak transcription Enhancers Bivalent Enhancer Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs548371956	chr12:341296-341297	Weak transcription Enhancers Bivalent Enhancer Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs190979024	chr12:341298-341299	Weak transcription Enhancers Bivalent Enhancer Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs570078889	chr12:341343-341344	Weak transcription Enhancers Bivalent Enhancer Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs143110859	chr12:341348-341349	Weak transcription Enhancers Bivalent Enhancer Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs511230	chr12:341376-341377	Weak transcription Enhancers Bivalent Enhancer Genic enhancers	n/a	n/a	Overlapped CNVs	mRNA abundance
17	rs3782862	chr12:341392-341393	Weak transcription Enhancers Bivalent Enhancer Genic enhancers	n/a	n/a	Overlapped CNVs	mRNA abundance
18	rs148221459	chr12:341431-341432	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs553569455	chr12:341432-341433	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs574918840	chr12:341438-341439	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs541933544	chr12:341441-341442	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs183827994	chr12:341547-341548	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs556774024	chr12:341548-341549	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs141188585	chr12:341596-341597	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs3782861	chr12:341686-341687	Weak transcription Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs564063742	chr12:341695-341696	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs186757224	chr12:341699-341700	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs191434487	chr12:341705-341706	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs35788657	chr12:341706-341707	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs561574901	chr12:341742-341743	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs182809340	chr12:341769-341770	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs186712986	chr12:341804-341805	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs531260895	chr12:341813-341814	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs189610166	chr12:341821-341822	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs573129232	chr12:341822-341823	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs371698356	chr12:341873-341874	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs150301423	chr12:341911-341912	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs371569348	chr12:341932-341933	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs137935803	chr12:341997-341998	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs11615492	chr12:342004-342005	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs565276415	chr12:342073-342074	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs182144937	chr12:342106-342107	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs34077284	chr12:342130-342131	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs187913733	chr12:342148-342149	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs146923788	chr12:342151-342152	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs568681524	chr12:342183-342184	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs544605191	chr12:342209-342210	Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs193092843	chr12:342232-342233	Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs185297251	chr12:342251-342252	Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs562705731	chr12:342284-342285	Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:84)

Disease	PMID	Source
Cancer	20164920	CNVD
Myelofibrosis	22110671	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Glaucoma	21310917	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Malignant peripheral nerve sheath tumor	19844265	CNVD
Squamous cell cancer	19607727	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Hepatocellular carcinoma	16750200	CNVD
Breast cancer	17133270	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Mental retardation	17847001	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
abnormal development	18461090	CNVD
Ovarian cancer	20844748	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Medulloblastoma	16968546	CNVD
Ovine squamous-cell carcinoma	17599052	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
small cell lung cancer	20016488	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Breast cancer	21364760	CNVD
Developmental delay	21147756	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Ewing''s sarcoma	17952124	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Acute myeloid leukemia	20729466	CNVD
Breast cancer	21858162	CNVD
Breast cancer	21509527	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21785460	CNVD
Autism	22495309	CNVD
Ovarian cancer	21720365	CNVD
Myelodysplastic syndrome	21251322	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:431 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:337400-343000	Enhancers	Brain Hippocampus Middle	brain
2	chr12:337800-341400	Enhancers	Brain Anterior Caudate	brain
3	chr12:338200-341200	Enhancers	Cortex derived primary cultured neurospheres	brain
4	chr12:338600-343000	Enhancers	Fetal Brain Male	brain
5	chr12:339000-343400	Enhancers	Fetal Muscle Leg	muscle
6	chr12:339000-343400	Enhancers	HSMMtube	muscle
7	chr12:339400-341800	Enhancers	Skeletal Muscle Male	skeletal muscle
8	chr12:339800-341600	Enhancers	Brain Cingulate Gyrus	brain
9	chr12:339800-343200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
10	chr12:340000-342800	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
11	chr12:340200-341200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
12	chr12:340200-341600	Enhancers	Brain Angular Gyrus	brain
13	chr12:340200-342000	Enhancers	Skeletal Muscle Female	skeletal muscle
14	chr12:340400-341200	Enhancers	Fetal Brain Female	brain
15	chr12:340400-342600	Enhancers	Breast Myoepithelial Primary Cells	Breast
16	chr12:340400-343400	Enhancers	Brain Germinal Matrix	brain
17	chr12:340600-342600	Enhancers	HepG2	liver
18	chr12:340600-343600	Enhancers	Fetal Muscle Trunk	muscle
19	chr12:340800-341400	Enhancers	Brain Inferior Temporal Lobe	brain
20	chr12:340800-341800	Genic enhancers	Liver	Liver
21	chr12:340800-341800	Enhancers	Brain Substantia Nigra	brain
22	chr12:340800-342200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
23	chr12:340800-342400	Weak transcription	H1 Cell Line	embryonic stem cell
24	chr12:341000-342000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
25	chr12:341000-342000	Weak transcription	Psoas Muscle	Psoas
26	chr12:341200-341400	Bivalent Enhancer	Cortex derived primary cultured neurospheres	brain
27	chr12:341200-341800	Weak transcription	Fetal Brain Female	brain
28	chr12:341600-342600	Weak transcription	Brain Angular Gyrus	brain
29	chr12:341800-342800	Enhancers	Fetal Brain Female	brain
30	chr12:341800-343000	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
31	chr12:341800-344200	Enhancers	Liver	Liver
32	chr12:342000-342600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
33	chr12:342000-343200	Enhancers	Psoas Muscle	Psoas
34	chr12:342000-343200	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
35	chr12:342200-342800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
36	chr12:342200-343200	Bivalent Enhancer	H9 Derived Neuron Cultured Cells	ES cell derived
37	chr12:342400-342600	Bivalent Enhancer	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
38	chr12:342400-342800	Bivalent Enhancer	Fetal Stomach	stomach
39	chr12:342400-343000	Enhancers	H1 Cell Line	embryonic stem cell
40	chr12:342400-343000	Enhancers	Placenta	Placenta
41	chr12:342600-342800	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
42	chr12:342600-342800	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin01	Skin
43	chr12:342600-342800	Enhancers	Brain Angular Gyrus	brain
44	chr12:342600-343000	Bivalent Enhancer	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
45	chr12:342800-343000	Weak transcription	Brain Angular Gyrus	brain
46	chr12:342800-354600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
47	chr12:343000-343400	Enhancers	Skeletal Muscle Male	skeletal muscle
48	chr12:343000-344200	Weak transcription	Brain Hippocampus Middle	brain
49	chr12:343200-343400	Enhancers	Brain Inferior Temporal Lobe	brain
50	chr12:343200-343600	Enhancers	Skeletal Muscle Female	skeletal muscle

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