Variant report

Variant	esv3363784
Chromosome Location	chr12:7951537-8058518
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1700)
CpG islands
(count:1099)
Chromatin interactive
region (count:15)
LncRNA
region (count:7)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1700 , 50 per page) page: 1 2 3 4 5 6 7 ... 34

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr12:7984728-7985022	K562	blood:	n/a	n/a
2	ARID3A	chr12:7984707-7984990	HepG2	liver:	n/a	n/a
3	ARID3A	chr12:7959548-7959804	HepG2	liver:	n/a	n/a
4	ARID3A	chr12:8043247-8043927	HepG2	liver:	n/a	n/a
5	ARID3A	chr12:7959526-7959828	K562	blood:	n/a	n/a
6	ARID3A	chr12:8057729-8058351	HepG2	liver:	n/a	n/a
7	ARID3A	chr12:8003917-8004749	HepG2	liver:	n/a	n/a
8	ATF1	chr12:8017264-8017507	K562	blood:	n/a	n/a
9	ATF1	chr12:7996816-7996880	K562	blood:	n/a	n/a
10	ATF1	chr12:8021845-8022067	K562	blood:	n/a	n/a
11	ATF1	chr12:8043615-8043923	K562	blood:	n/a	n/a
12	ATF2	chr12:8058108-8058451	H1-hESC	embryonic stem cell:	n/a	n/a
13	ATF2	chr12:8058161-8058458	H1-hESC	embryonic stem cell:	n/a	n/a
14	ATF2	chr12:8042996-8043524	H1-hESC	embryonic stem cell:	n/a	n/a
15	ATF2	chr12:8012580-8013428	H1-hESC	embryonic stem cell:	n/a	n/a
16	ATF2	chr12:8012535-8013325	H1-hESC	embryonic stem cell:	n/a	n/a
17	ATF3	chr12:8043693-8043923	K562	blood:	n/a	n/a
18	BACH1	chr12:8009353-8009400	H1-hESC	embryonic stem cell:	n/a	n/a
19	BATF	chr12:8012531-8012835	GM12878	blood:	n/a	n/a
20	BCL11A	chr12:8012546-8012846	GM12878	blood:	n/a	chr12:8012761-8012770
21	BHLHE40	chr12:7959591-7959830	K562	blood:	n/a	n/a
22	BHLHE40	chr12:8004230-8004592	HepG2	liver:	n/a	n/a
23	BHLHE40	chr12:8004272-8004591	HepG2	liver:	n/a	n/a
24	BHLHE40	chr12:8040472-8040534	K562	blood:	n/a	n/a
25	BHLHE40	chr12:8017224-8017578	K562	blood:	n/a	n/a
26	BHLHE40	chr12:8012724-8012773	GM12878	blood:	n/a	n/a
27	BHLHE40	chr12:8053551-8053638	K562	blood:	n/a	n/a
28	BRCA1	chr12:8013131-8013375	Hela-S3	cervix:	n/a	n/a
29	BRCA1	chr12:8043651-8043833	Hela-S3	cervix:	n/a	n/a
30	CCNT2	chr12:8021795-8022050	K562	blood:	n/a	n/a
31	CEBPB	chr12:8043613-8044051	MCF-7	breast:	n/a	n/a
32	CEBPB	chr12:7987335-7987623	HepG2	liver:	n/a	n/a
33	CEBPB	chr12:8038727-8038973	IMR90	lung:	n/a	chr12:8038813-8038824
34	CEBPB	chr12:8043613-8043918	K562	blood:	n/a	n/a
35	CEBPB	chr12:8013012-8013531	A549	lung:	n/a	n/a
36	CEBPB	chr12:7987300-7987985	HepG2	liver:	n/a	n/a
37	CEBPB	chr12:8038793-8038861	A549	lung:	n/a	chr12:8038813-8038824
38	CEBPB	chr12:8013133-8013534	A549	lung:	n/a	n/a
39	CEBPB	chr12:8012586-8013610	H1-hESC	embryonic stem cell:	n/a	n/a
40	CEBPB	chr12:8038737-8038981	Hela-S3	cervix:	n/a	chr12:8038813-8038824
41	CEBPB	chr12:8038614-8038897	K562	blood:	n/a	chr12:8038813-8038824
42	CEBPB	chr12:8013026-8013621	IMR90	lung:	n/a	n/a
43	CEBPB	chr12:8038718-8038987	HepG2	liver:	n/a	chr12:8038813-8038824
44	CEBPB	chr12:7987334-7987689	MCF-7	breast:	n/a	n/a
45	CEBPB	chr12:8021811-8022031	H1-hESC	embryonic stem cell:	n/a	n/a
46	CEBPB	chr12:8038710-8038905	HepG2	liver:	n/a	chr12:8038813-8038824
47	CEBPB	chr12:8013033-8013601	Hela-S3	cervix:	n/a	n/a
48	CEBPB	chr12:8043717-8043936	K562	blood:	n/a	n/a
49	CEBPB	chr12:8043667-8043953	H1-hESC	embryonic stem cell:	n/a	n/a
50	CEBPB	chr12:8043194-8044014	HepG2	liver:	n/a	n/a

(count:1099 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:8025582-8025632	NB4	blood:	n/a
2	chr12:8025582-8025632	NB4	blood:	n/a
3	chr12:8025861-8025911	HCM	heart:	n/a
4	chr12:8028945-8028995	ECC-1	luminal epithelium:	n/a
5	chr12:8022108-8022158	NB4	blood:	n/a
6	chr12:8025861-8025911	IMR90	lung:	fetal
7	chr12:8023676-8023726	U87	brain:	n/a
8	chr12:7966784-7966834	K562	blood:	n/a
9	chr12:8025646-8025696	NHDF-neo	bronchial:	n/a
10	chr12:8043600-8043650	HNPCEpiC	eye:	n/a
11	chr12:8025567-8025617	SKMC	muscle:	n/a
12	chr12:8026515-8026565	SK-N-SH_RA	brain:	n/a
13	chr12:8025567-8025617	HNPCEpiC	eye:	n/a
14	chr12:8025517-8025567	SAEC	small airway:	n/a
15	chr12:8025593-8025643	NT2-D1	testis:	n/a
16	chr12:8022108-8022158	AG04449	skin:	fetal
17	chr12:7966784-7966834	NHBE	bronchial:	n/a
18	chr12:8015791-8015841	HRPEpiC	eye:	n/a
19	chr12:8015903-8015953	AG10803	skin:	n/a
20	chr12:8025394-8025444	BE2_C	brain:	n/a
21	chr12:8025567-8025617	CMK	blood:	n/a
22	chr12:8026515-8026565	ovcar-3	ovarian:	n/a
23	chr12:8025640-8025690	NH-A	brain:	n/a
24	chr12:8015903-8015953	HCF	heart:	n/a
25	chr12:8025394-8025444	GM12878	blood:	n/a
26	chr12:8025394-8025444	AG09319	gingival:	n/a
27	chr12:8022108-8022158	HEK293	kidney:	embryo
28	chr12:8012926-8012976	HRCEpiC	kidney:	n/a
29	chr12:8023676-8023726	GM06990	blood:	n/a
30	chr12:8025861-8025911	Jurkat	blood:	n/a
31	chr12:8025861-8025911	HEEpiC	esophagus:	n/a
32	chr12:8015903-8015953	HCT-116	colon:	n/a
33	chr12:8043600-8043650	SKMC	muscle:	n/a
34	chr12:8023676-8023726	NT2-D1	testis:	n/a
35	chr12:8043600-8043650	SAEC	small airway:	n/a
36	chr12:8015103-8015153	NB4	blood:	n/a
37	chr12:8025861-8025911	AG10803	skin:	n/a
38	chr12:8025567-8025617	MCF10A-Er-Src	breast:	n/a
39	chr12:8025861-8025911	H1-hESC	embryonic stem cell:	embryo
40	chr12:7966784-7966834	ECC-1	luminal epithelium:	n/a
41	chr12:8012926-8012976	SK-N-MC	brain:	n/a
42	chr12:8023676-8023726	HAEpiC	amniotic membrane:	n/a
43	chr12:8026515-8026565	PFSK-1	brain:	n/a
44	chr12:8025517-8025567	HAEpiC	amniotic membrane:	n/a
45	chr12:8043600-8043650	BJ	skin:	n/a
46	chr12:8012926-8012976	Caco-2	colon:	n/a
47	chr12:8025567-8025617	PrEC	prostate:	n/a
48	chr12:8028945-8028995	HEK293	kidney:	embryo
49	chr12:8025646-8025696	HCPEpiC	choroid plexus:	n/a
50	chr12:8025593-8025643	SK-N-SH	brain:	n/a

(count:15 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:8036991..8037615-chr12:8067883..8068385,2	MCF-7	breast:
2	chr12:8021089..8023625-chr12:8037749..8040054,2	MCF-7	breast:
3	chr12:7868671..7869617-chr12:7959225..7960025,4	MCF-7	breast:
4	chr12:8012297..8013140-chr12:8147611..8148236,3	K562	blood:
5	chr12:8053022..8053940-chr12:8067825..8068746,2	MCF-7	breast:
6	chr12:7797730..7798285-chr12:7959327..7960129,2	MCF-7	breast:
7	chr12:7830039..7830628-chr12:7959515..7960112,3	K562	blood:
8	chr12:8010803..8012757-chr12:8088381..8089897,2	K562	blood:
9	chr12:7985856..7986361-chr12:8086765..8087460,2	Hela-S3	cervix:
10	chr12:8012482..8013075-chr12:8147622..8148284,2	MCF-7	breast:
11	chr12:7869134..7869702-chr12:7959145..7959716,2	MCF-7	breast:
12	chr12:8037350..8037880-chr12:8072256..8073016,2	MCF-7	breast:
13	chr12:7785661..7787296-chr12:7958245..7961143,2	K562	blood:
14	chr12:7829622..7830601-chr12:7959144..7960112,6	MCF-7	breast:
15	chr12:8043777..8046059-chr12:8052507..8054935,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SLC2A3-2	chr12:8024469-8024544	NONHSAT026272
2	lnc-SLC2A3-2	chr12:8023446-8023658	NONHSAT026272
3	lnc-SLC2A3-2	chr12:8023775-8023879	NONHSAT026272
4	lnc-SLC2A14-1	chr12:8049210-8049554	NONHSAT026273
5	lnc-SLC2A3-2	chr12:8025403-8025460	NONHSAT026272
6	lnc-NANOGP1-1	chr12:8052070-8052674	NONHSAT026274
7	lnc-NANOGP1-2	chr12:8013033-8013360	NONHSAT026271

No data

Variant related genes	Relation type
ENSG00000201663	TF binding region
ENSG00000241828	TF binding region
SLC2A14	TF binding region
NANOGP1	TF binding region
ENSG00000222978	TF binding region
ENSG00000255885	TF binding region
ENSG00000255356	TF binding region
ENSG00000199912	TF binding region
ENSG00000201663	CpG island
ENSG00000241828	CpG island
SLC2A14	CpG island
NANOGP1	CpG island
ENSG00000222978	CpG island
ENSG00000255885	CpG island
ENSG00000255356	CpG island
ENSG00000199912	CpG island
ENSG00000176654	chromatin interactions
ENSG00000059804	chromatin interactions
ENSG00000255885	chromatin interactions
ENSG00000240739	chromatin interactions

Extended variants
information (count: 3315 )
Associated
traits (count: 89 )

Variant overlapped rSNPs/rCNVs (count:3315 , 50 per page) page: 1 2 3 4 5 6 7 ... 67

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs147861447	chr12:7951707-7951708	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs189306478	chr12:7951711-7951712	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs141329818	chr12:7951725-7951726	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs7311015	chr12:7951729-7951730	Weak transcription Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs7302398	chr12:7951738-7951739	Weak transcription Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs374155832	chr12:7951750-7951751	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs35740633	chr12:7951783-7951784	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs35050917	chr12:7951784-7951785	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs72518424	chr12:7951785-7951786	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs397764510	chr12:7951786-7951787	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs11833213	chr12:7951835-7951836	Genic enhancers Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs146990722	chr12:7951861-7951862	Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs576333634	chr12:7951906-7951907	Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs35140537	chr12:7951978-7951979	Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs376525970	chr12:7951979-7951980	Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs74058871	chr12:7951986-7951987	Genic enhancers Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs11055839	chr12:7951987-7951988	Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs7137943	chr12:7952013-7952014	Genic enhancers Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs11830990	chr12:7952080-7952081	Genic enhancers Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs192340821	chr12:7952091-7952092	Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs574415891	chr12:7952131-7952132	Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs11055840	chr12:7952133-7952134	Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs185565269	chr12:7952151-7952152	Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs369469125	chr12:7952160-7952161	Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs114404567	chr12:7952171-7952172	Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs190442396	chr12:7952182-7952183	Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs201329729	chr12:7952214-7952215	Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs371595007	chr12:7952215-7952216	Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs11055842	chr12:7952219-7952220	Genic enhancers Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs112265869	chr12:7952224-7952225	Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs145887668	chr12:7952228-7952229	Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs376272101	chr12:7952240-7952241	Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs138494334	chr12:7952319-7952320	Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs73270973	chr12:7952321-7952322	Genic enhancers Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs116430960	chr12:7952331-7952332	Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs111412087	chr12:7952355-7952356	Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs76628183	chr12:7952356-7952357	Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs201917982	chr12:7952357-7952358	Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs376547137	chr12:7952358-7952359	Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs58792327	chr12:7952359-7952360	Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs146112600	chr12:7952397-7952398	Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs140142409	chr12:7952408-7952409	Genic enhancers Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs185997959	chr12:7952420-7952421	Genic enhancers Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs34718019	chr12:7952431-7952432	Genic enhancers Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs34126011	chr12:7952449-7952450	Genic enhancers Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs189253777	chr12:7952455-7952456	Genic enhancers Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs60847050	chr12:7952460-7952461	Genic enhancers Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs200285147	chr12:7952470-7952471	Genic enhancers Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs58296602	chr12:7952471-7952472	Genic enhancers Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs534742433	chr12:7952474-7952475	Genic enhancers Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:89)

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
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Cancer	20164919	CNVD
Epilepsy	21858020	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Breast cancer	21364760	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
Medullary thyroid carcinoma	18765511	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	17289997	CNVD
Nasopharyngeal cancer	20548289	CNVD
Type 2 diabetes	21526130	CNVD
Autism	22495309	CNVD
Bipolar disorder	19214233	CNVD
Schizophrenia	20967226	CNVD
early-passage human iPS cells	21368824	CNVD
Williams Syndrome	20824207	CNVD
Ependymoma	20639864	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Glioma	20126413	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:1117 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:7944000-7953200	Weak transcription	Right Atrium	heart
2	chr12:7947400-7956800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
3	chr12:7949200-7953200	Genic enhancers	HUES6 Cell Line	embryonic stem cell
4	chr12:7950000-7951800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
5	chr12:7950200-7952400	Genic enhancers	HUES48 Cell Line	embryonic stem cell
6	chr12:7950200-7953200	Enhancers	iPS-15b Cell Line	embryonic stem cell
7	chr12:7950400-7951800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
8	chr12:7950400-7960800	Weak transcription	Stomach Mucosa	stomach
9	chr12:7950600-7951800	Enhancers	HUES64 Cell Line	embryonic stem cell
10	chr12:7950600-7952000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
11	chr12:7950800-7952200	Enhancers	iPS-18 Cell Line	embryonic stem cell
12	chr12:7950800-7952200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
13	chr12:7951000-7951800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
14	chr12:7951000-7957600	Weak transcription	H9 Cell Line	embryonic stem cell
15	chr12:7951000-7959800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
16	chr12:7951200-7951800	Weak transcription	H1 Cell Line	embryonic stem cell
17	chr12:7951200-7952000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
18	chr12:7951200-7952200	Enhancers	iPS-20b Cell Line	embryonic stem cell
19	chr12:7951200-7969200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
20	chr12:7951400-7953200	Enhancers	HepG2	liver
21	chr12:7951800-7952600	Genic enhancers	HUES64 Cell Line	embryonic stem cell
22	chr12:7951800-7952800	Enhancers	H1 Cell Line	embryonic stem cell
23	chr12:7951800-7953200	Genic enhancers	ES-I3 Cell Line	embryonic stem cell
24	chr12:7951800-7957800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
25	chr12:7952000-7953200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
26	chr12:7952200-7952400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
27	chr12:7952200-7952400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
28	chr12:7952200-7952800	Genic enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
29	chr12:7952200-7954000	Genic enhancers	iPS-18 Cell Line	embryonic stem cell
30	chr12:7952400-7955600	Strong transcription	HUES48 Cell Line	embryonic stem cell
31	chr12:7952400-7955800	Strong transcription	iPS-20b Cell Line	embryonic stem cell
32	chr12:7952600-7954000	Strong transcription	HUES64 Cell Line	embryonic stem cell
33	chr12:7952800-7953200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
34	chr12:7952800-7953600	Weak transcription	H1 Cell Line	embryonic stem cell
35	chr12:7953200-7953600	Strong transcription	iPS DF 19.11 Cell Line	embryonic stem cell
36	chr12:7953200-7954000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
37	chr12:7953200-7954200	Weak transcription	HepG2	liver
38	chr12:7953200-7954800	Strong transcription	HUES6 Cell Line	embryonic stem cell
39	chr12:7953200-7957600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
40	chr12:7953200-7957600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
41	chr12:7953600-7953800	Genic enhancers	H1 Cell Line	embryonic stem cell
42	chr12:7953600-7987400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
43	chr12:7953800-7954200	Strong transcription	H1 Cell Line	embryonic stem cell
44	chr12:7954000-7954400	Strong transcription	ES-I3 Cell Line	embryonic stem cell
45	chr12:7954000-7959200	Weak transcription	HUES64 Cell Line	embryonic stem cell
46	chr12:7954000-7959800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
47	chr12:7954200-7954400	Enhancers	HepG2	liver
48	chr12:7954200-7957600	Weak transcription	H1 Cell Line	embryonic stem cell
49	chr12:7954400-7957600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
50	chr12:7954800-7957600	Weak transcription	HUES6 Cell Line	embryonic stem cell

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