Variant report

Variant	nsv557275
Chromosome Location	chr12:7953089-8057923
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1614)
CpG islands
(count:1100)
Chromatin interactive
region (count:15)
LncRNA
region (count:7)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1614 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr12:7959548-7959804	HepG2	liver:	n/a	n/a
2	ARID3A	chr12:8057729-8058351	HepG2	liver:	n/a	n/a
3	ARID3A	chr12:7959526-7959828	K562	blood:	n/a	n/a
4	ARID3A	chr12:7984728-7985022	K562	blood:	n/a	n/a
5	ARID3A	chr12:8003917-8004749	HepG2	liver:	n/a	n/a
6	ARID3A	chr12:8043247-8043927	HepG2	liver:	n/a	n/a
7	ARID3A	chr12:7984707-7984990	HepG2	liver:	n/a	n/a
8	ATF1	chr12:8043615-8043923	K562	blood:	n/a	n/a
9	ATF1	chr12:7996816-7996880	K562	blood:	n/a	n/a
10	ATF1	chr12:8017264-8017507	K562	blood:	n/a	n/a
11	ATF1	chr12:8021845-8022067	K562	blood:	n/a	n/a
12	ATF2	chr12:8012535-8013325	H1-hESC	embryonic stem cell:	n/a	n/a
13	ATF2	chr12:8012580-8013428	H1-hESC	embryonic stem cell:	n/a	n/a
14	ATF2	chr12:8042996-8043524	H1-hESC	embryonic stem cell:	n/a	n/a
15	ATF3	chr12:8043693-8043923	K562	blood:	n/a	n/a
16	BACH1	chr12:8009353-8009400	H1-hESC	embryonic stem cell:	n/a	n/a
17	BATF	chr12:8012531-8012835	GM12878	blood:	n/a	n/a
18	BCL11A	chr12:8012546-8012846	GM12878	blood:	n/a	chr12:8012761-8012770
19	BHLHE40	chr12:8053551-8053638	K562	blood:	n/a	n/a
20	BHLHE40	chr12:8012724-8012773	GM12878	blood:	n/a	n/a
21	BHLHE40	chr12:8040472-8040534	K562	blood:	n/a	n/a
22	BHLHE40	chr12:8017224-8017578	K562	blood:	n/a	n/a
23	BHLHE40	chr12:8004230-8004592	HepG2	liver:	n/a	n/a
24	BHLHE40	chr12:8004272-8004591	HepG2	liver:	n/a	n/a
25	BHLHE40	chr12:7959591-7959830	K562	blood:	n/a	n/a
26	BRCA1	chr12:8013131-8013375	Hela-S3	cervix:	n/a	n/a
27	BRCA1	chr12:8043651-8043833	Hela-S3	cervix:	n/a	n/a
28	CCNT2	chr12:8021795-8022050	K562	blood:	n/a	n/a
29	CEBPB	chr12:8043650-8043983	A549	lung:	n/a	n/a
30	CEBPB	chr12:8038703-8038938	MCF-7	breast:	n/a	chr12:8038813-8038824
31	CEBPB	chr12:7987335-7987623	HepG2	liver:	n/a	n/a
32	CEBPB	chr12:8021766-8022066	A549	lung:	n/a	n/a
33	CEBPB	chr12:7987387-7987701	MCF-7	breast:	n/a	n/a
34	CEBPB	chr12:8013133-8013534	A549	lung:	n/a	n/a
35	CEBPB	chr12:8013026-8013621	IMR90	lung:	n/a	n/a
36	CEBPB	chr12:8021808-8022088	Hela-S3	cervix:	n/a	n/a
37	CEBPB	chr12:8043613-8043918	K562	blood:	n/a	n/a
38	CEBPB	chr12:8043503-8044096	A549	lung:	n/a	n/a
39	CEBPB	chr12:8012161-8012797	IMR90	lung:	n/a	n/a
40	CEBPB	chr12:7987300-7987985	HepG2	liver:	n/a	n/a
41	CEBPB	chr12:8043667-8043953	H1-hESC	embryonic stem cell:	n/a	n/a
42	CEBPB	chr12:8043615-8044065	A549	lung:	n/a	n/a
43	CEBPB	chr12:8038710-8038905	HepG2	liver:	n/a	chr12:8038813-8038824
44	CEBPB	chr12:8043613-8044051	MCF-7	breast:	n/a	n/a
45	CEBPB	chr12:7987790-7988017	H1-hESC	embryonic stem cell:	n/a	n/a
46	CEBPB	chr12:8038660-8038991	HepG2	liver:	n/a	chr12:8038813-8038824
47	CEBPB	chr12:8043717-8043936	K562	blood:	n/a	n/a
48	CEBPB	chr12:8013012-8013531	A549	lung:	n/a	n/a
49	CEBPB	chr12:7987334-7987689	MCF-7	breast:	n/a	n/a
50	CEBPB	chr12:7996233-7996412	IMR90	lung:	n/a	n/a

(count:1100 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:8022108-8022158	HRCEpiC	kidney:	n/a
2	chr12:8025640-8025690	GM19239	blood:	n/a
3	chr12:8022108-8022158	HRCEpiC	kidney:	n/a
4	chr12:8025640-8025690	GM19239	blood:	n/a
5	chr12:8028945-8028995	NB4	blood:	n/a
6	chr12:8025640-8025690	AG10803	skin:	n/a
7	chr12:8043600-8043650	AG09309	skin:	n/a
8	chr12:8025567-8025617	H1-hESC	embryonic stem cell:	embryo
9	chr12:8025593-8025643	PrEC	prostate:	n/a
10	chr12:8026515-8026565	AG04449	skin:	fetal
11	chr12:8022108-8022158	GM06990	blood:	n/a
12	chr12:8015103-8015153	HL-60	blood:	n/a
13	chr12:8025394-8025444	HEEpiC	esophagus:	n/a
14	chr12:8015103-8015153	Jurkat	blood:	n/a
15	chr12:8015791-8015841	RPTEC	kidney:	n/a
16	chr12:8025567-8025617	A549	lung:	n/a
17	chr12:8023676-8023726	ovcar-3	ovarian:	n/a
18	chr12:8025582-8025632	GM19239	blood:	n/a
19	chr12:8025394-8025444	HRE	kidney:	n/a
20	chr12:8026515-8026565	PrEC	prostate:	n/a
21	chr12:8043600-8043650	IMR90	lung:	fetal
22	chr12:8015791-8015841	HNPCEpiC	eye:	n/a
23	chr12:7966784-7966834	NH-A	brain:	n/a
24	chr12:8023676-8023726	HMEC	breast:	n/a
25	chr12:8015903-8015953	HCT-116	colon:	n/a
26	chr12:8025394-8025444	SKMC	muscle:	n/a
27	chr12:8015903-8015953	SKMC	muscle:	n/a
28	chr12:7966784-7966834	SK-N-SH	brain:	n/a
29	chr12:8023676-8023726	GM19239	blood:	n/a
30	chr12:8028945-8028995	SK-N-SH	brain:	n/a
31	chr12:8025861-8025911	PFSK-1	brain:	n/a
32	chr12:8025517-8025567	HCPEpiC	choroid plexus:	n/a
33	chr12:8015791-8015841	U87	brain:	n/a
34	chr12:8025582-8025632	SKMC	muscle:	n/a
35	chr12:8025582-8025632	HepG2	liver:	n/a
36	chr12:7966784-7966834	HEEpiC	esophagus:	n/a
37	chr12:8025582-8025632	SK-N-MC	brain:	n/a
38	chr12:8015903-8015953	IMR90	lung:	fetal
39	chr12:8023676-8023726	HAEpiC	amniotic membrane:	n/a
40	chr12:8043600-8043650	NHBE	bronchial:	n/a
41	chr12:8025517-8025567	HMEC	breast:	n/a
42	chr12:8022108-8022158	MCF10A-Er-Src	breast:	n/a
43	chr12:8015903-8015953	HCF	heart:	n/a
44	chr12:8026515-8026565	NB4	blood:	n/a
45	chr12:8015791-8015841	K562	blood:	n/a
46	chr12:8023676-8023726	HRPEpiC	eye:	n/a
47	chr12:8025861-8025911	BE2_C	brain:	n/a
48	chr12:7966784-7966834	T-47D	breast:	n/a
49	chr12:8022108-8022158	AG10803	skin:	n/a
50	chr12:8025593-8025643	AG04450	lung:	fetal

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

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

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

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

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
ENSG00000059804	chromatin interactions
ENSG00000240739	chromatin interactions
ENSG00000255885	chromatin interactions
ENSG00000176654	chromatin interactions

Extended variants
information (count: 3215 )
Associated
traits (count: 89 )

Variant overlapped rSNPs/rCNVs (count:3215 , 50 per page) page: 1 2 3 4 5 6 7 ... 65

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7300262	chr12:7953089-7953090	Genic enhancers Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs7306487	chr12:7953128-7953129	Genic enhancers Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs7310214	chr12:7953135-7953136	Genic enhancers Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs182636113	chr12:7953140-7953141	Genic enhancers Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs7310227	chr12:7953169-7953170	Genic enhancers Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs7310234	chr12:7953177-7953178	Genic enhancers Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs148927750	chr12:7953229-7953230	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs186226130	chr12:7953269-7953270	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs143310683	chr12:7953290-7953291	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs71038765	chr12:7953295-7953296	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs386760033	chr12:7953315-7953316	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs7310369	chr12:7953316-7953317	Weak transcription Strong transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs6488655	chr12:7953360-7953361	Weak transcription Strong transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs147072652	chr12:7953433-7953434	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs144802076	chr12:7953436-7953437	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs71038766	chr12:7953451-7953452	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs11055848	chr12:7953452-7953453	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs371122752	chr12:7953456-7953457	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs367966290	chr12:7953501-7953502	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs571735765	chr12:7953636-7953637	Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs7310857	chr12:7953653-7953654	Weak transcription Genic enhancers Strong transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs11055851	chr12:7953696-7953697	Weak transcription Genic enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs145657743	chr12:7953725-7953726	Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs138233264	chr12:7953730-7953731	Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs200975116	chr12:7953765-7953766	Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs374161955	chr12:7953766-7953767	Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs377179316	chr12:7953792-7953793	Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs190806948	chr12:7953869-7953870	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs116582917	chr12:7953872-7953873	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs371930440	chr12:7953912-7953913	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs183446571	chr12:7953949-7953950	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs552871905	chr12:7953962-7953963	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs566298768	chr12:7953990-7953991	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs7301419	chr12:7953997-7953998	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs2110088	chr12:7954035-7954036	Strong transcription Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs74058873	chr12:7954039-7954040	Strong transcription Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs111636037	chr12:7954043-7954044	Strong transcription Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs1990482	chr12:7954051-7954052	Strong transcription Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
39	rs187345477	chr12:7954170-7954171	Strong transcription Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs386760034	chr12:7954220-7954221	Strong transcription Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs192144629	chr12:7954222-7954223	Strong transcription Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs5796289	chr12:7954330-7954331	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs34951409	chr12:7954357-7954358	Strong transcription Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs1990481	chr12:7954360-7954361	Strong transcription Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs183080964	chr12:7954376-7954377	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs5796290	chr12:7954459-7954460	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs3040870	chr12:7954460-7954461	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs566748517	chr12:7954461-7954462	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs139787435	chr12:7954462-7954463	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs375425920	chr12:7954472-7954473	Weak transcription 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:1089 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

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	chr12:7950200-7953200	Enhancers	iPS-15b Cell Line	embryonic stem cell
5	chr12:7950400-7960800	Weak transcription	Stomach Mucosa	stomach
6	chr12:7951000-7957600	Weak transcription	H9 Cell Line	embryonic stem cell
7	chr12:7951000-7959800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
8	chr12:7951200-7969200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
9	chr12:7951400-7953200	Enhancers	HepG2	liver
10	chr12:7951800-7953200	Genic enhancers	ES-I3 Cell Line	embryonic stem cell
11	chr12:7951800-7957800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
12	chr12:7952000-7953200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
13	chr12:7952200-7954000	Genic enhancers	iPS-18 Cell Line	embryonic stem cell
14	chr12:7952400-7955600	Strong transcription	HUES48 Cell Line	embryonic stem cell
15	chr12:7952400-7955800	Strong transcription	iPS-20b Cell Line	embryonic stem cell
16	chr12:7952600-7954000	Strong transcription	HUES64 Cell Line	embryonic stem cell
17	chr12:7952800-7953200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
18	chr12:7952800-7953600	Weak transcription	H1 Cell Line	embryonic stem cell
19	chr12:7953200-7953600	Strong transcription	iPS DF 19.11 Cell Line	embryonic stem cell
20	chr12:7953200-7954000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
21	chr12:7953200-7954200	Weak transcription	HepG2	liver
22	chr12:7953200-7954800	Strong transcription	HUES6 Cell Line	embryonic stem cell
23	chr12:7953200-7957600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
24	chr12:7953200-7957600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
25	chr12:7953600-7953800	Genic enhancers	H1 Cell Line	embryonic stem cell
26	chr12:7953600-7987400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
27	chr12:7953800-7954200	Strong transcription	H1 Cell Line	embryonic stem cell
28	chr12:7954000-7954400	Strong transcription	ES-I3 Cell Line	embryonic stem cell
29	chr12:7954000-7959200	Weak transcription	HUES64 Cell Line	embryonic stem cell
30	chr12:7954000-7959800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
31	chr12:7954200-7954400	Enhancers	HepG2	liver
32	chr12:7954200-7957600	Weak transcription	H1 Cell Line	embryonic stem cell
33	chr12:7954400-7957600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
34	chr12:7954800-7957600	Weak transcription	HUES6 Cell Line	embryonic stem cell
35	chr12:7955600-7957600	Weak transcription	HUES48 Cell Line	embryonic stem cell
36	chr12:7955800-7956400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
37	chr12:7956400-7956600	Strong transcription	iPS-20b Cell Line	embryonic stem cell
38	chr12:7956600-7958000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
39	chr12:7957600-7957800	Enhancers	ES-I3 Cell Line	embryonic stem cell
40	chr12:7957600-7957800	Enhancers	H1 Cell Line	embryonic stem cell
41	chr12:7957600-7957800	Enhancers	H9 Cell Line	embryonic stem cell
42	chr12:7957600-7957800	Enhancers	HUES48 Cell Line	embryonic stem cell
43	chr12:7957600-7958000	Enhancers	HUES6 Cell Line	embryonic stem cell
44	chr12:7957600-7958000	Enhancers	iPS-15b Cell Line	embryonic stem cell
45	chr12:7957600-7958200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
46	chr12:7957600-7958400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
47	chr12:7957600-7958400	Enhancers	NH-A	brain
48	chr12:7957600-7959200	Enhancers	NHDF-Ad	bronchial
49	chr12:7957600-7959400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
50	chr12:7957600-7959600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

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