Variant report

Variant	nsv898623
Chromosome Location	chr12:4751798-4771456
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:479)
CpG islands
(count:794)
Chromatin interactive
region (count:21)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:479 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr12:4757430-4758315	K562	blood:	n/a	n/a
2	ATF2	chr12:4757999-4758491	H1-hESC	embryonic stem cell:	n/a	n/a
3	ATF2	chr12:4757972-4758620	GM12878	blood:	n/a	n/a
4	ATF2	chr12:4758070-4758634	GM12878	blood:	n/a	n/a
5	BCLAF1	chr12:4757941-4758505	GM12878	blood:	n/a	chr12:4758114-4758123
6	BCLAF1	chr12:4757913-4758630	GM12878	blood:	n/a	chr12:4758114-4758123
7	BHLHE40	chr12:4758013-4758504	GM12878	blood:	n/a	n/a
8	BHLHE40	chr12:4757761-4758471	K562	blood:	n/a	n/a
9	BHLHE40	chr12:4757362-4757603	GM12878	blood:	n/a	n/a
10	BRCA1	chr12:4757522-4758889	Hela-S3	cervix:	n/a	n/a
11	CCNT2	chr12:4757956-4758363	K562	blood:	n/a	n/a
12	CEBPB	chr12:4758026-4758412	H1-hESC	embryonic stem cell:	n/a	n/a
13	CEBPB	chr12:4759955-4760222	HepG2	liver:	n/a	chr12:4760126-4760137 chr12:4760126-4760139 chr12:4760127-4760138
14	CEBPB	chr12:4759436-4759663	HepG2	liver:	n/a	n/a
15	CEBPB	chr12:4757830-4757894	K562	blood:	n/a	n/a
16	CEBPB	chr12:4760017-4760288	K562	blood:	n/a	chr12:4760126-4760137 chr12:4760126-4760139 chr12:4760127-4760138
17	CEBPD	chr12:4758143-4758473	HepG2	liver:	n/a	n/a
18	CHD1	chr12:4757476-4758871	H1-hESC	embryonic stem cell:	n/a	n/a
19	CHD2	chr12:4758078-4758446	GM12878	blood:	n/a	n/a
20	CHD2	chr12:4758193-4758446	HepG2	liver:	n/a	n/a
21	CHD2	chr12:4757737-4757887	K562	blood:	n/a	n/a
22	CHD2	chr12:4758021-4758466	H1-hESC	embryonic stem cell:	n/a	n/a
23	CHD2	chr12:4757626-4758623	Hela-S3	cervix:	n/a	n/a
24	CREB1	chr12:4757960-4758541	H1-hESC	embryonic stem cell:	n/a	n/a
25	CREB1	chr12:4758112-4758477	A549	lung:	n/a	n/a
26	CREB1	chr12:4758078-4758323	A549	lung:	n/a	n/a
27	CREB1	chr12:4754210-4754564	H1-hESC	embryonic stem cell:	n/a	n/a
28	CTCF	chr12:4762420-4762570	HVMF	connective:	n/a	n/a
29	CTCF	chr12:4757436-4757457	GM10266	blood:	n/a	n/a
30	CTCF	chr12:4757980-4758130	NHLF	lung:	n/a	n/a
31	CTCF	chr12:4762440-4762590	AG04449	skin:	n/a	n/a
32	CTCF	chr12:4762380-4762530	HMEC	breast:	n/a	n/a
33	CTCF	chr12:4764900-4765050	NHEK	skin:	n/a	n/a
34	CTCF	chr12:4762360-4762510	AG04450	lung:	n/a	n/a
35	CTCF	chr12:4757660-4757810	A549	lung:	n/a	n/a
36	CTCF	chr12:4762420-4762570	HRPEpiC	eye:	n/a	n/a
37	CTCF	chr12:4758740-4758890	Caco-2	colon:	n/a	n/a
38	CTCF	chr12:4758079-4758321	K562	blood:	n/a	n/a
39	CTCF	chr12:4757748-4757758	K562	blood:	n/a	n/a
40	CTCF	chr12:4758195-4758285	Kidney_OC	kidney:	n/a	n/a
41	CTCF	chr12:4762460-4762610	HA-sp	spinal cord:	n/a	n/a
42	CTCF	chr12:4762400-4762550	HRPEpiC	eye:	n/a	n/a
43	CTCF	chr12:4762500-4762650	HEK293	kidney:	n/a	n/a
44	CTCF	chr12:4758165-4758206	Spleen_OC	spleen:	n/a	n/a
45	CTCF	chr12:4762460-4762610	HCPEpiC	choroid plexus:	n/a	n/a
46	CTCF	chr12:4758162-4758291	GM12878	blood:	n/a	n/a
47	CTCF	chr12:4762380-4762530	HPAF	blood vessel:	n/a	n/a
48	CTCF	chr12:4762460-4762610	RPTEC	kidney:	n/a	n/a
49	CTCF	chr12:4762380-4762530	Caco-2	colon:	n/a	n/a
50	CTCF	chr12:4762500-4762650	AG10803	skin:	n/a	n/a

(count:794 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:4757728-4757778	U87	brain:	n/a
2	chr12:4757728-4757778	U87	brain:	n/a
3	chr12:4754247-4754297	NHDF-neo	bronchial:	n/a
4	chr12:4758201-4758251	NHDF-neo	bronchial:	n/a
5	chr12:4758272-4758322	CMK	blood:	n/a
6	chr12:4762206-4762256	PrEC	prostate:	n/a
7	chr12:4754247-4754297	AG10803	skin:	n/a
8	chr12:4757717-4757767	HCPEpiC	choroid plexus:	n/a
9	chr12:4758272-4758322	H1-hESC	embryonic stem cell:	embryo
10	chr12:4762206-4762256	RPTEC	kidney:	n/a
11	chr12:4754247-4754297	AG04449	skin:	fetal
12	chr12:4755479-4755529	ECC-1	luminal epithelium:	n/a
13	chr12:4758496-4758546	HIPEpiC	eye:	n/a
14	chr12:4758424-4758474	GM06990	blood:	n/a
15	chr12:4758201-4758251	HEEpiC	esophagus:	n/a
16	chr12:4758272-4758322	HEEpiC	esophagus:	n/a
17	chr12:4758217-4758267	HIPEpiC	eye:	n/a
18	chr12:4755555-4755605	NB4	blood:	n/a
19	chr12:4757728-4757778	RPTEC	kidney:	n/a
20	chr12:4754247-4754297	GM12891	blood:	n/a
21	chr12:4755479-4755529	IMR90	lung:	fetal
22	chr12:4755479-4755529	Caco-2	colon:	n/a
23	chr12:4757728-4757778	BE2_C	brain:	n/a
24	chr12:4758496-4758546	NH-A	brain:	n/a
25	chr12:4757717-4757767	HUVEC	blood vessel:	n/a
26	chr12:4755555-4755605	MCF-7	breast:	n/a
27	chr12:4758496-4758546	SK-N-MC	brain:	n/a
28	chr12:4758496-4758546	GM06990	blood:	n/a
29	chr12:4758217-4758267	CMK	blood:	n/a
30	chr12:4762206-4762256	A549	lung:	n/a
31	chr12:4754247-4754297	A549	lung:	n/a
32	chr12:4755555-4755605	AoSMC	blood vessel:	n/a
33	chr12:4757759-4757809	HAEpiC	amniotic membrane:	n/a
34	chr12:4757717-4757767	ovcar-3	ovarian:	n/a
35	chr12:4757728-4757778	MCF-7	breast:	n/a
36	chr12:4758250-4758300	NHBE	bronchial:	n/a
37	chr12:4755479-4755529	SAEC	small airway:	n/a
38	chr12:4757728-4757778	HRPEpiC	eye:	n/a
39	chr12:4755479-4755529	AG04449	skin:	fetal
40	chr12:4757728-4757778	MCF10A-Er-Src	breast:	n/a
41	chr12:4757759-4757809	NH-A	brain:	n/a
42	chr12:4758272-4758322	HL-60	blood:	n/a
43	chr12:4755555-4755605	GM19239	blood:	n/a
44	chr12:4758496-4758546	PrEC	prostate:	n/a
45	chr12:4758250-4758300	GM06990	blood:	n/a
46	chr12:4758250-4758300	PFSK-1	brain:	n/a
47	chr12:4758250-4758300	IMR90	lung:	fetal
48	chr12:4757759-4757809	HRCEpiC	kidney:	n/a
49	chr12:4758201-4758251	BJ	skin:	n/a
50	chr12:4758272-4758322	MCF-7	breast:	n/a

(count:21 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:4754845..4760714-chr12:4761830..4765057,7	MCF-7	breast:
2	chr12:4762857..4765662-chr12:4767685..4769794,2	K562	blood:
3	chr12:4758381..4761405-chr12:4778974..4782071,3	K562	blood:
4	chr12:4757537..4758351-chr2:9983167..9983703,2	Hela-S3	cervix:
5	chr12:4757063..4759938-chr12:4760465..4764038,5	K562	blood:
6	chr12:4762857..4765662-chr12:4767685..4769794,2	K562	blood:
7	chr12:4762342..4764303-chr12:4764418..4767058,2	K562	blood:
8	chr12:4757018..4762059-chr12:4764285..4767290,6	K562	blood:
9	chr12:4751073..4755821-chr12:4757118..4761577,5	MCF-7	breast:
10	chr12:4756861..4759668-chr12:4760395..4765208,7	MCF-7	breast:
11	chr12:4757063..4759938-chr12:4760465..4764038,5	K562	blood:
12	chr12:4751073..4755821-chr12:4757118..4761577,5	MCF-7	breast:
13	chr12:4757989..4759732-chr12:4759874..4761785,2	MCF-7	breast:
14	chr12:4757018..4762059-chr12:4764285..4767290,6	K562	blood:
15	chr12:4762342..4764303-chr12:4764418..4767058,2	K562	blood:
16	chr12:4756861..4759668-chr12:4760395..4765208,7	MCF-7	breast:
17	chr12:4758240..4760595-chr12:4768074..4769785,2	K562	blood:
18	chr12:4757573..4759938-chr12:4760465..4764276,3	K562	blood:
19	chr12:4743724..4745923-chr12:4752293..4755038,2	K562	blood:
20	chr12:4754845..4760714-chr12:4761830..4765057,7	MCF-7	breast:
21	chr12:4757573..4759938-chr12:4760465..4764276,3	K562	blood:

(count:6 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RP11-234B24.6.1-1	chr12:4757002-4757193	ENSG00000256381
2	lnc-AKAP3-3	chr12:4757911-4758213	NONHSAT025967
3	lnc-AKAP3-3	chr12:4754221-4754358	NONHSAT025967
4	lnc-AKAP3-3	chr12:4757620-4758174	NONHSAT025968
5	lnc-AKAP3-3	chr12:4756240-4758165	NONHSAT025970
6	lnc-RP11-234B24.6.1-1	chr12:4754662-4755041	ENSG00000256381

No data

Variant related genes	Relation type
ENSG00000256381	TF binding region
NDUFA9	TF binding region
AKAP3	TF binding region
ENSG00000255639	TF binding region
ENSG00000256381	CpG island
NDUFA9	CpG island
AKAP3	CpG island
ENSG00000255639	CpG island
ENSG00000139180	chromatin interactions
ENSG00000256799	chromatin interactions
ENSG00000256381	chromatin interactions
ENSG00000255639	chromatin interactions
ENSG00000115750	chromatin interactions
ENSG00000111254	chromatin interactions

Extended variants
information (count: 734 )
Associated
traits (count: 77 )

Variant overlapped rSNPs/rCNVs (count:734 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10774255	chr12:4751798-4751799	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs186731927	chr12:4751810-4751811	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs536470325	chr12:4751821-4751822	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs7314381	chr12:4751841-4751842	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs569774074	chr12:4751854-4751855	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs7132398	chr12:4751858-4751859	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs558553311	chr12:4751867-4751868	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs139507579	chr12:4751881-4751882	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs541677057	chr12:4751886-4751887	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs554987789	chr12:4751902-4751903	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs149726447	chr12:4751917-4751918	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs111774401	chr12:4752093-4752094	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs563432855	chr12:4752095-4752096	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs191129906	chr12:4752129-4752130	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs183141176	chr12:4752149-4752150	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs559730795	chr12:4752161-4752162	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs71293105	chr12:4752279-4752280	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs7298334	chr12:4752377-4752378	Weak transcription	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs547640158	chr12:4752391-4752392	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs537951741	chr12:4752474-4752475	Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
21	rs376178904	chr12:4752557-4752558	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs529871726	chr12:4752590-4752591	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs539667658	chr12:4752617-4752618	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs112649171	chr12:4752643-4752644	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs550038827	chr12:4752692-4752693	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs111463047	chr12:4752698-4752699	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs117621074	chr12:4752764-4752765	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs74060087	chr12:4752811-4752812	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs558385737	chr12:4752828-4752829	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs565644288	chr12:4752882-4752883	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
31	rs534326684	chr12:4752915-4752916	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
32	rs555205507	chr12:4752916-4752917	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
33	rs574833799	chr12:4752923-4752924	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
34	rs570004282	chr12:4752927-4752928	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
35	rs537244890	chr12:4752940-4752941	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
36	rs557160444	chr12:4752992-4752993	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
37	rs112180716	chr12:4753062-4753063	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
38	rs546242717	chr12:4753088-4753089	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
39	rs559613201	chr12:4753092-4753093	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
40	rs187392693	chr12:4753102-4753103	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
41	rs555941501	chr12:4753165-4753166	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
42	rs12310365	chr12:4753199-4753200	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs535791187	chr12:4753243-4753244	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
44	rs146123845	chr12:4753282-4753283	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
45	rs142647650	chr12:4753313-4753314	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs530060424	chr12:4753317-4753318	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs549987806	chr12:4753348-4753349	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs147673684	chr12:4753368-4753369	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs532230515	chr12:4753373-4753374	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs61909961	chr12:4753501-4753502	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:77)

Disease	PMID	Source
Ovarian cancer	20844748	CNVD
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
low-grade B-cell lymphoma tumor	18367492	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
lymphocytic leukemia	21291569	CNVD
Adenocarcinoma	19607727	CNVD
Squamous cell cancer	19607727	CNVD
Epilepsy	21858020	CNVD
Colorectal cancer	19359472	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Breast cancer	21509527	CNVD
Prostate cancer	18632612	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Breast cancer	21364760	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:912 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:4724200-4756800	Weak transcription	Skeletal Muscle Male	skeletal muscle
2	chr12:4725400-4752200	Weak transcription	Brain Hippocampus Middle	brain
3	chr12:4737600-4757400	Weak transcription	Pancreas	Pancrea
4	chr12:4737800-4757200	Weak transcription	Brain Anterior Caudate	brain
5	chr12:4745400-4757200	Weak transcription	Brain Substantia Nigra	brain
6	chr12:4746600-4757000	Weak transcription	Small Intestine	intestine
7	chr12:4752800-4754000	Enhancers	GM12878-XiMat	blood
8	chr12:4754000-4754800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
9	chr12:4754000-4755000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
10	chr12:4754000-4756600	Weak transcription	GM12878-XiMat	blood
11	chr12:4754200-4754400	Enhancers	HUES6 Cell Line	embryonic stem cell
12	chr12:4754200-4754600	Enhancers	ES-I3 Cell Line	embryonic stem cell
13	chr12:4754200-4754800	Weak transcription	Aorta	Aorta
14	chr12:4754400-4757200	Weak transcription	HUES6 Cell Line	embryonic stem cell
15	chr12:4754600-4754800	Enhancers	iPS-15b Cell Line	embryonic stem cell
16	chr12:4754600-4756800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
17	chr12:4754800-4755000	ZNF genes & repeats	Aorta	Aorta
18	chr12:4754800-4757200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
19	chr12:4755000-4757000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
20	chr12:4755000-4757400	Weak transcription	Aorta	Aorta
21	chr12:4756400-4757000	Enhancers	Dnd41	blood
22	chr12:4756400-4757600	Enhancers	Sigmoid Colon	Sigmoid Colon
23	chr12:4756600-4756800	Enhancers	GM12878-XiMat	blood
24	chr12:4756600-4757200	Enhancers	Breast Myoepithelial Primary Cells	Breast
25	chr12:4756800-4757000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
26	chr12:4756800-4757000	Enhancers	HUES48 Cell Line	embryonic stem cell
27	chr12:4756800-4757000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
28	chr12:4756800-4757000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
29	chr12:4756800-4757000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
30	chr12:4756800-4757000	Enhancers	Brain Angular Gyrus	brain
31	chr12:4756800-4757000	Enhancers	Duodenum Mucosa	Duodenum
32	chr12:4756800-4757000	Enhancers	Fetal Intestine Large	intestine
33	chr12:4756800-4757000	Active TSS	Rectal Mucosa Donor 29	rectum
34	chr12:4756800-4757000	Active TSS	Skeletal Muscle Male	skeletal muscle
35	chr12:4756800-4757000	Enhancers	HMEC	breast
36	chr12:4756800-4757000	Enhancers	NHEK	skin
37	chr12:4756800-4757200	Enhancers	ES-I3 Cell Line	embryonic stem cell
38	chr12:4756800-4757200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
39	chr12:4756800-4757200	Enhancers	Primary B cells from cord blood	blood
40	chr12:4756800-4757200	Enhancers	Primary hematopoietic stem cells short term culture	blood
41	chr12:4756800-4757200	Enhancers	Fetal Intestine Small	intestine
42	chr12:4756800-4757200	Enhancers	Fetal Kidney	kidney
43	chr12:4756800-4757200	Enhancers	Pancreatic Islets	Pancreatic Islet
44	chr12:4756800-4757200	Enhancers	Skeletal Muscle Female	skeletal muscle
45	chr12:4756800-4757200	Enhancers	HepG2	liver
46	chr12:4756800-4757400	Enhancers	iPS-15b Cell Line	embryonic stem cell
47	chr12:4756800-4757400	Enhancers	Liver	Liver
48	chr12:4756800-4757400	Enhancers	Placenta Amnion	Placenta Amnion
49	chr12:4756800-4757400	Enhancers	Stomach Mucosa	stomach
50	chr12:4756800-4757400	Enhancers	Thymus	Thymus

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