Variant report

Variant	nsv527083
Chromosome Location	chr2:9797994-9810648
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:178)
CpG islands
(count:183)
Chromatin interactive
region (count:13)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:178 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CEBPB	chr2:9797952-9798224	A549	lung:	n/a	n/a
2	CEBPB	chr2:9797971-9798237	HepG2	liver:	n/a	n/a
3	CEBPB	chr2:9798079-9798200	H1-hESC	embryonic stem cell:	n/a	n/a
4	CREB1	chr2:9806000-9806410	A549	lung:	n/a	n/a
5	CTCF	chr2:9797960-9798110	RPTEC	kidney:	n/a	chr2:9798088-9798097
6	CTCF	chr2:9798045-9798130	MCF-7	breast:	n/a	chr2:9798088-9798097
7	CTCF	chr2:9798020-9798170	GM12864	blood:	n/a	chr2:9798088-9798097
8	CTCF	chr2:9805920-9806070	HCPEpiC	choroid plexus:	n/a	n/a
9	CTCF	chr2:9798000-9798150	HBMEC	blood vessel:	n/a	chr2:9798088-9798097
10	CTCF	chr2:9798000-9798150	HAc	cerebellar:	n/a	chr2:9798088-9798097
11	CTCF	chr2:9798060-9798210	HCPEpiC	choroid plexus:	n/a	chr2:9798088-9798097
12	CTCF	chr2:9799160-9799310	HEEpiC	esophagus:	n/a	n/a
13	CTCF	chr2:9806020-9806170	A549	lung:	n/a	n/a
14	CTCF	chr2:9806160-9806310	AG04449	skin:	n/a	n/a
15	CTCF	chr2:9797958-9798215	K562	blood:	n/a	chr2:9798088-9798097
16	CTCF	chr2:9806040-9806190	BJ	skin:	n/a	n/a
17	CTCF	chr2:9798120-9798270	AoAF	blood vessel:	n/a	n/a
18	CTCF	chr2:9798006-9798172	Hela-S3	cervix:	n/a	chr2:9798088-9798097
19	CTCF	chr2:9798000-9798150	HRPEpiC	eye:	n/a	chr2:9798088-9798097
20	CTCF	chr2:9797980-9798130	HCT-116	colon:	n/a	chr2:9798088-9798097
21	CTCF	chr2:9798060-9798210	HepG2	liver:	n/a	chr2:9798088-9798097
22	CTCF	chr2:9797995-9798176	K562	blood:	n/a	chr2:9798088-9798097
23	CTCF	chr2:9797933-9798170	A549	lung:	n/a	chr2:9798088-9798097
24	CTCF	chr2:9798000-9798150	HEK293	kidney:	n/a	chr2:9798088-9798097
25	CTCF	chr2:9798000-9798150	HPAF	blood vessel:	n/a	chr2:9798088-9798097
26	CTCF	chr2:9798003-9798187	GM12878	blood:	n/a	chr2:9798088-9798097
27	CTCF	chr2:9798040-9798190	Caco-2	colon:	n/a	chr2:9798088-9798097
28	CTCF	chr2:9798100-9798250	A549	lung:	n/a	n/a
29	CTCF	chr2:9798020-9798170	MCF-7	breast:	n/a	chr2:9798088-9798097
30	CTCF	chr2:9798100-9798250	HEEpiC	esophagus:	n/a	n/a
31	CTCF	chr2:9798060-9798210	AG10803	skin:	n/a	chr2:9798088-9798097
32	CTCF	chr2:9798080-9798230	MCF-7	breast:	n/a	chr2:9798088-9798097
33	CTCF	chr2:9798020-9798170	HepG2	liver:	n/a	chr2:9798088-9798097
34	CTCF	chr2:9798020-9798170	SAEC	small airway:	n/a	chr2:9798088-9798097
35	CTCF	chr2:9798020-9798170	Hela-S3	cervix:	n/a	chr2:9798088-9798097
36	CTCF	chr2:9798040-9798190	HL-60	blood:	n/a	chr2:9798088-9798097
37	CTCF	chr2:9806100-9806250	AG10803	skin:	n/a	n/a
38	CTCF	chr2:9798040-9798190	GM12873	blood:	n/a	chr2:9798088-9798097
39	CTCF	chr2:9798000-9798150	BJ	skin:	n/a	chr2:9798088-9798097
40	CTCF	chr2:9797979-9798149	Medullo	brain:	n/a	chr2:9798088-9798097
41	CTCF	chr2:9806040-9806190	HBMEC	blood vessel:	n/a	n/a
42	CTCF	chr2:9797980-9798130	WERI-Rb-1	eye:	n/a	chr2:9798088-9798097
43	CTCF	chr2:9798020-9798170	K562	blood:	n/a	chr2:9798088-9798097
44	CTCF	chr2:9797951-9798275	K562	blood:	n/a	chr2:9798088-9798097
45	CTCF	chr2:9798040-9798190	HBMEC	blood vessel:	n/a	chr2:9798088-9798097
46	CTCF	chr2:9798020-9798170	WERI-Rb-1	eye:	n/a	chr2:9798088-9798097
47	CTCF	chr2:9798020-9798170	AG10803	skin:	n/a	chr2:9798088-9798097
48	CTCF	chr2:9798020-9798170	HRE	kidney:	n/a	chr2:9798088-9798097
49	CTCF	chr2:9798020-9798170	AG09309	skin:	n/a	chr2:9798088-9798097
50	CTCF	chr2:9806180-9806330	HMF	breast:	n/a	n/a

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:9800511-9800561	PANC-1	pancreas:	n/a
2	chr2:9800511-9800561	GM12892	blood:	n/a
3	chr2:9800556-9800606	T-47D	breast:	n/a
4	chr2:9800556-9800606	SKMC	muscle:	n/a
5	chr2:9800511-9800561	H1-hESC	embryonic stem cell:	embryo
6	chr2:9800511-9800561	GM06990	blood:	n/a
7	chr2:9800451-9800501	H1-hESC	embryonic stem cell:	embryo
8	chr2:9800556-9800606	Jurkat	blood:	n/a
9	chr2:9800556-9800606	PrEC	prostate:	n/a
10	chr2:9800451-9800501	T-47D	breast:	n/a
11	chr2:9800556-9800606	A549	lung:	n/a
12	chr2:9800511-9800561	AG10803	skin:	n/a
13	chr2:9800451-9800501	HIPEpiC	eye:	n/a
14	chr2:9800451-9800501	HRCEpiC	kidney:	n/a
15	chr2:9800451-9800501	HCF	heart:	n/a
16	chr2:9800556-9800606	Hela-S3	cervix:	n/a
17	chr2:9800451-9800501	BE2_C	brain:	n/a
18	chr2:9800511-9800561	SAEC	small airway:	n/a
19	chr2:9800556-9800606	HEEpiC	esophagus:	n/a
20	chr2:9800511-9800561	HCPEpiC	choroid plexus:	n/a
21	chr2:9800511-9800561	Hepatocyte	liver:	n/a
22	chr2:9800556-9800606	NT2-D1	testis:	n/a
23	chr2:9800451-9800501	NHDF-neo	bronchial:	n/a
24	chr2:9800511-9800561	IMR90	lung:	fetal
25	chr2:9800556-9800606	NHBE	bronchial:	n/a
26	chr2:9800451-9800501	HEK293	kidney:	embryo
27	chr2:9800511-9800561	HUVEC	blood vessel:	n/a
28	chr2:9800556-9800606	NHDF-neo	bronchial:	n/a
29	chr2:9800556-9800606	MCF-7	breast:	n/a
30	chr2:9800556-9800606	HCPEpiC	choroid plexus:	n/a
31	chr2:9800556-9800606	GM12891	blood:	n/a
32	chr2:9800556-9800606	HEK293	kidney:	embryo
33	chr2:9800556-9800606	AoSMC	blood vessel:	n/a
34	chr2:9800451-9800501	NH-A	brain:	n/a
35	chr2:9800511-9800561	NT2-D1	testis:	n/a
36	chr2:9800511-9800561	ovcar-3	ovarian:	n/a
37	chr2:9800556-9800606	HRPEpiC	eye:	n/a
38	chr2:9800556-9800606	HUVEC	blood vessel:	n/a
39	chr2:9800511-9800561	Caco-2	colon:	n/a
40	chr2:9800556-9800606	SK-N-MC	brain:	n/a
41	chr2:9800511-9800561	BJ	skin:	n/a
42	chr2:9800556-9800606	ECC-1	luminal epithelium:	n/a
43	chr2:9800511-9800561	GM12878	blood:	n/a
44	chr2:9800451-9800501	K562	blood:	n/a
45	chr2:9800556-9800606	BE2_C	brain:	n/a
46	chr2:9800556-9800606	HPAEpiC	pulmonary alveolar:	n/a
47	chr2:9800451-9800501	HAEpiC	amniotic membrane:	n/a
48	chr2:9800511-9800561	SK-N-SH_RA	brain:	n/a
49	chr2:9800511-9800561	MCF10A-Er-Src	breast:	n/a
50	chr2:9800511-9800561	HRCEpiC	kidney:	n/a

(count:13 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:9803885..9806660-chr2:9808908..9811665,2	K562	blood:
2	chr2:9770939..9772938-chr2:9810123..9813246,3	MCF-7	breast:
3	chr2:9797605..9799669-chr2:9803320..9804886,2	MCF-7	breast:
4	chr2:9803309..9805079-chr2:9808643..9811328,2	MCF-7	breast:
5	chr2:9803309..9805079-chr2:9808643..9811328,2	MCF-7	breast:
6	chr2:9797495..9799232-chr2:9803127..9805069,2	K562	blood:
7	chr2:9771970..9774412-chr2:9797666..9799794,2	K562	blood:
8	chr2:9796534..9798886-chr2:9908745..9911045,3	K562	blood:
9	chr2:9792147..9794483-chr2:9799893..9802301,3	K562	blood:
10	chr2:9797605..9799669-chr2:9803320..9804886,2	MCF-7	breast:
11	chr2:9782654..9789334-chr2:9794560..9799702,7	MCF-7	breast:
12	chr2:9797495..9799232-chr2:9803127..9805069,2	K562	blood:
13	chr2:9803885..9806660-chr2:9808908..9811665,2	K562	blood:

No data

Variant related genes	Relation type
ENSG00000244260	TF binding region
ENSG00000244260	CpG island
ENSG00000134308	chromatin interactions
ENSG00000243491	chromatin interactions

Extended variants
information (count: 550 )
Associated
traits (count: 56 )

Variant overlapped rSNPs/rCNVs (count:550 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4669407	chr2:9797994-9797995	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs574042336	chr2:9797998-9797999	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs140007326	chr2:9798076-9798077	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs377205648	chr2:9798080-9798081	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs74624110	chr2:9798097-9798098	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs576297812	chr2:9798100-9798101	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs6712680	chr2:9798106-9798107	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs190803175	chr2:9798124-9798125	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs4668627	chr2:9798142-9798143	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs73157516	chr2:9798156-9798157	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs560661056	chr2:9798208-9798209	Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs182033225	chr2:9798215-9798216	Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs565520679	chr2:9798230-9798231	Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs75571238	chr2:9798244-9798245	Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs186205838	chr2:9798264-9798265	Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs142986298	chr2:9798275-9798276	Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs563189949	chr2:9798283-9798284	Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs113468590	chr2:9798338-9798339	Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs7576067	chr2:9798396-9798397	Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs375101542	chr2:9798397-9798398	Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs571843151	chr2:9798402-9798403	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs557196297	chr2:9798409-9798410	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs369573779	chr2:9798419-9798420	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs534409966	chr2:9798507-9798508	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs547864371	chr2:9798539-9798540	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs567806583	chr2:9798555-9798556	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs576139789	chr2:9798582-9798583	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs6432028	chr2:9798592-9798593	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs6432029	chr2:9798599-9798600	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs149437909	chr2:9798603-9798604	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs538526042	chr2:9798611-9798612	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs113035146	chr2:9798616-9798617	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs571867080	chr2:9798619-9798620	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs57786001	chr2:9798641-9798642	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs111727587	chr2:9798642-9798643	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs181502738	chr2:9798643-9798644	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs543390360	chr2:9798651-9798652	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs563165935	chr2:9798654-9798655	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs139835037	chr2:9798725-9798726	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs11900302	chr2:9798760-9798761	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs565579009	chr2:9798804-9798805	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs527883984	chr2:9798805-9798806	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs572053683	chr2:9798814-9798815	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs567746609	chr2:9798861-9798862	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs185745711	chr2:9798864-9798865	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs72777070	chr2:9798877-9798878	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs373104844	chr2:9798910-9798911	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs539030565	chr2:9798915-9798916	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs73162688	chr2:9798943-9798944	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs143268697	chr2:9798963-9798964	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:56)

Disease	PMID	Source
Breast cancer	17133270	CNVD
Mental retardation	17847001	CNVD
Glioblastoma multiforme	21080181	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Cancer	20164920	CNVD
Neuroblastoma	21508638	CNVD
Breast cancer	17603634	CNVD
Cancer	16751803	CNVD
Neuroblastoma	16790693	CNVD
Colorectal cancer	16272173	CNVD
Breast cancer	17393978	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Medulloblastoma	21979893	CNVD
Lynch syndrome	18415027	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17387387	CNVD
Neuroblastoma	17533364	CNVD
Neuroblastoma	18923191	CNVD
Endometrial cancer	22040021	CNVD
Adrenal tumor	17535989	CNVD
Breast cancer	21264507	CNVD
Basal cell lymphoma	17053054	CNVD
Medulloblastoma	17522785	CNVD
Cancer	23418310	CNVD
Ewing''s sarcoma	21437220	CNVD
Ependymoma	16718352	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
lymphocytic leukemia	21291569	CNVD
Prostate cancer	18632612	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Bladder cancer	21909424	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Cancer	20164919	CNVD
Hodgkin''s lymphoma	18641027	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Breast cancer	21364760	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Follicular lymphoma	20505157	CNVD
Autism	17483303	CNVD
Breast cancer	21804112	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	22286061	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Glioma	17123091	CNVD
Breast cancer	20409316	CNVD
Multiple myeloma	16616336	CNVD
Myofibroblastic sarcoma	19369631	CNVD

Chromatin state (count:236 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:9790800-9799200	Weak transcription	H1 Cell Line	embryonic stem cell
2	chr2:9790800-9801000	Weak transcription	HUES6 Cell Line	embryonic stem cell
3	chr2:9792800-9801600	Weak transcription	Spleen	Spleen
4	chr2:9794200-9799400	Enhancers	HMEC	breast
5	chr2:9794400-9798000	Enhancers	NHLF	lung
6	chr2:9794400-9799600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
7	chr2:9794400-9800400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
8	chr2:9794600-9798400	Enhancers	NHDF-Ad	bronchial
9	chr2:9794600-9799600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
10	chr2:9794800-9799000	Weak transcription	Placenta	Placenta
11	chr2:9794800-9800400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
12	chr2:9795000-9798000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr2:9795000-9798600	Weak transcription	Fetal Muscle Trunk	muscle
14	chr2:9795000-9799200	Enhancers	Osteobl	bone
15	chr2:9795200-9798000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
16	chr2:9795400-9798000	Flanking Active TSS	A549	lung
17	chr2:9795400-9798200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
18	chr2:9795400-9798200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
19	chr2:9795400-9799200	Enhancers	HSMM	muscle
20	chr2:9795600-9799200	Enhancers	HSMMtube	muscle
21	chr2:9796200-9798200	Enhancers	Hela-S3	cervix
22	chr2:9796200-9798400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
23	chr2:9796600-9798000	Enhancers	NH-A	brain
24	chr2:9796600-9799600	Enhancers	Muscle Satellite Cultured Cells	--
25	chr2:9796800-9798200	Enhancers	ES-WA7 Cell Line	embryonic stem cell
26	chr2:9796800-9799600	Enhancers	Fetal Muscle Leg	muscle
27	chr2:9797000-9798200	Enhancers	Ovary	ovary
28	chr2:9797000-9799400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
29	chr2:9797000-9799400	Enhancers	GM12878-XiMat	blood
30	chr2:9797000-9802400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
31	chr2:9797200-9798000	Weak transcription	HUES64 Cell Line	embryonic stem cell
32	chr2:9797200-9798000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
33	chr2:9797400-9798400	Enhancers	ES-I3 Cell Line	embryonic stem cell
34	chr2:9797400-9798400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
35	chr2:9797600-9798200	Bivalent Enhancer	HepG2	liver
36	chr2:9797600-9798800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
37	chr2:9797600-9798800	Weak transcription	NHEK	skin
38	chr2:9797600-9802200	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
39	chr2:9797800-9798000	Enhancers	iPS-18 Cell Line	embryonic stem cell
40	chr2:9797800-9808800	Weak transcription	Pancreas	Pancrea
41	chr2:9798000-9798200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
42	chr2:9798000-9798200	Enhancers	H9 Cell Line	embryonic stem cell
43	chr2:9798000-9798200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
44	chr2:9798000-9798400	Enhancers	HUES64 Cell Line	embryonic stem cell
45	chr2:9798000-9798400	Weak transcription	NH-A	brain
46	chr2:9798000-9799200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
47	chr2:9798000-9799400	Enhancers	A549	lung
48	chr2:9798000-9799600	Enhancers	Skeletal Muscle Female	skeletal muscle
49	chr2:9798000-9803200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
50	chr2:9798200-9798400	Bivalent Enhancer	ES-WA7 Cell Line	embryonic stem cell

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