Variant report

Variant	nsv975866
Chromosome Location	chr11:104994182-105034480
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:256)
CpG islands
(count:428)
Chromatin interactive
region (count:1)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:256 , 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	chr11:105015639-105015977	HepG2	liver:	n/a	n/a
2	BRCA1	chr11:105003141-105004166	Hela-S3	cervix:	n/a	chr11:105003219-105003226
3	CEBPB	chr11:104996917-104997136	Hela-S3	cervix:	n/a	n/a
4	CEBPB	chr11:105003406-105004606	Hela-S3	cervix:	n/a	n/a
5	CEBPB	chr11:105026850-105027169	HepG2	liver:	n/a	n/a
6	CEBPB	chr11:105021042-105021282	A549	lung:	n/a	chr11:105021130-105021141
7	CEBPB	chr11:105003565-105003848	IMR90	lung:	n/a	n/a
8	CEBPB	chr11:104996913-104997165	A549	lung:	n/a	n/a
9	CEBPB	chr11:105026867-105027253	Hela-S3	cervix:	n/a	chr11:105027229-105027240
10	CEBPB	chr11:105029570-105029888	HepG2	liver:	n/a	chr11:105029701-105029712
11	CEBPB	chr11:105022935-105023276	HepG2	liver:	n/a	chr11:105023107-105023118 chr11:105023123-105023134
12	CEBPB	chr11:105021083-105021294	HepG2	liver:	n/a	chr11:105021130-105021141
13	CEBPB	chr11:105022487-105023313	IMR90	lung:	n/a	chr11:105023107-105023118 chr11:105023123-105023134
14	CEBPB	chr11:105029635-105029866	IMR90	lung:	n/a	chr11:105029701-105029712
15	CEBPB	chr11:104996949-104997149	HepG2	liver:	n/a	n/a
16	CEBPB	chr11:105022378-105023742	Hela-S3	cervix:	n/a	chr11:105023107-105023118 chr11:105023123-105023134
17	CEBPB	chr11:105015646-105016016	IMR90	lung:	n/a	n/a
18	CEBPB	chr11:105015618-105016048	Hela-S3	cervix:	n/a	n/a
19	CHD2	chr11:105003412-105003784	Hela-S3	cervix:	n/a	n/a
20	CHD2	chr11:105022850-105023619	Hela-S3	cervix:	n/a	n/a
21	CTCF	chr11:105001000-105001150	HEEpiC	esophagus:	n/a	n/a
22	CTCF	chr11:105026560-105026710	SAEC	small airway:	n/a	n/a
23	CTCF	chr11:105001005-105001184	GM19238	blood:	n/a	n/a
24	CTCF	chr11:105000960-105001110	GM06990	blood:	n/a	n/a
25	CTCF	chr11:105000940-105001090	GM12872	blood:	n/a	n/a
26	CTCF	chr11:105001020-105001170	GM12864	blood:	n/a	n/a
27	CTCF	chr11:105001020-105001170	GM06990	blood:	n/a	n/a
28	CTCF	chr11:105001051-105001186	GM13977	blood:	n/a	n/a
29	CTCF	chr11:105000980-105001130	GM12874	blood:	n/a	n/a
30	CTCF	chr11:105000980-105001130	NB4	blood:	n/a	n/a
31	CTCF	chr11:105001000-105001150	GM12875	blood:	n/a	n/a
32	CTCF	chr11:105001020-105001170	GM12873	blood:	n/a	n/a
33	CTCF	chr11:105017276-105017336	GM13976	blood:	n/a	n/a
34	CTCF	chr11:105000940-105001090	GM12873	blood:	n/a	n/a
35	CTCF	chr11:105001040-105001190	GM12868	blood:	n/a	n/a
36	CTCF	chr11:105001120-105001270	SAEC	small airway:	n/a	n/a
37	CTCF	chr11:105001020-105001170	GM12871	blood:	n/a	n/a
38	CTCF	chr11:105001080-105001230	NHEK	skin:	n/a	n/a
39	CTCF	chr11:105001080-105001106	ProgFib	skin:	n/a	n/a
40	CTCF	chr11:105001020-105001170	BE2_C	brain:	n/a	n/a
41	CTCF	chr11:105000940-105001090	GM12870	blood:	n/a	n/a
42	CTCF	chr11:105000940-105001090	GM12864	blood:	n/a	n/a
43	CTCF	chr11:105001023-105001173	GM19239	blood:	n/a	n/a
44	CTCF	chr11:105001000-105001150	GM12867	blood:	n/a	n/a
45	CTCF	chr11:105000960-105001110	GM12871	blood:	n/a	n/a
46	CTCF	chr11:105000960-105001110	HEK293	kidney:	n/a	n/a
47	CTCF	chr11:105000880-105001030	A549	lung:	n/a	n/a
48	CTCF	chr11:105001040-105001190	GM12866	blood:	n/a	n/a
49	CTCF	chr11:105001000-105001150	GM12873	blood:	n/a	n/a
50	CTCF	chr11:105001020-105001170	GM12865	blood:	n/a	n/a

(count:428 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:105011637-105011687	Hela-S3	cervix:	n/a
2	chr11:105011637-105011687	Hela-S3	cervix:	n/a
3	chr11:105011637-105011687	GM12891	blood:	n/a
4	chr11:105011637-105011687	AG10803	skin:	n/a
5	chr11:105009375-105009425	NHDF-neo	bronchial:	n/a
6	chr11:105011637-105011687	HNPCEpiC	eye:	n/a
7	chr11:105015202-105015252	AG04449	skin:	fetal
8	chr11:105022900-105022950	Jurkat	blood:	n/a
9	chr11:105010531-105010581	AG04449	skin:	fetal
10	chr11:105022900-105022950	PANC-1	pancreas:	n/a
11	chr11:105011637-105011687	HRPEpiC	eye:	n/a
12	chr11:105010531-105010581	IMR90	lung:	fetal
13	chr11:105010463-105010513	Caco-2	colon:	n/a
14	chr11:105022900-105022950	GM12878	blood:	n/a
15	chr11:105015202-105015252	MCF-7	breast:	n/a
16	chr11:105015202-105015252	HL-60	blood:	n/a
17	chr11:105011637-105011687	SK-N-SH	brain:	n/a
18	chr11:105015202-105015252	Jurkat	blood:	n/a
19	chr11:105010284-105010334	HPAEpiC	pulmonary alveolar:	n/a
20	chr11:105022900-105022950	U87	brain:	n/a
21	chr11:105015202-105015252	GM19239	blood:	n/a
22	chr11:105010531-105010581	AoSMC	blood vessel:	n/a
23	chr11:105009375-105009425	ProgFib	skin:	n/a
24	chr11:105010531-105010581	AG09309	skin:	n/a
25	chr11:105009375-105009425	HepG2	liver:	n/a
26	chr11:105010463-105010513	Jurkat	blood:	n/a
27	chr11:105010531-105010581	K562	blood:	n/a
28	chr11:105010463-105010513	MCF-7	breast:	n/a
29	chr11:105010531-105010581	GM06990	blood:	n/a
30	chr11:105010284-105010334	GM12892	blood:	n/a
31	chr11:105011637-105011687	Hepatocyte	liver:	n/a
32	chr11:105022900-105022950	NB4	blood:	n/a
33	chr11:105022900-105022950	PFSK-1	brain:	n/a
34	chr11:105010284-105010334	SAEC	small airway:	n/a
35	chr11:105010284-105010334	PFSK-1	brain:	n/a
36	chr11:105009375-105009425	H1-hESC	embryonic stem cell:	embryo
37	chr11:105010531-105010581	GM12892	blood:	n/a
38	chr11:105010284-105010334	PANC-1	pancreas:	n/a
39	chr11:105010463-105010513	AoSMC	blood vessel:	n/a
40	chr11:105010284-105010334	GM12878	blood:	n/a
41	chr11:105015202-105015252	HMEC	breast:	n/a
42	chr11:105015202-105015252	HUVEC	blood vessel:	n/a
43	chr11:105009375-105009425	HNPCEpiC	eye:	n/a
44	chr11:105010284-105010334	NH-A	brain:	n/a
45	chr11:105015202-105015252	SK-N-MC	brain:	n/a
46	chr11:105022900-105022950	HMEC	breast:	n/a
47	chr11:105009375-105009425	HUVEC	blood vessel:	n/a
48	chr11:105022900-105022950	AG09319	gingival:	n/a
49	chr11:105010284-105010334	HMEC	breast:	n/a
50	chr11:105010463-105010513	HRE	kidney:	n/a

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr11:105000203..105002774-chr11:105190534..105192628,2	K562	blood:

(count:2 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CARD18-2	chr11:105028654-105028817	ENSG00000254998.1
2	lnc-CARD18-2	chr11:105030992-105031083	ENSG00000254998.1

No data

Variant related genes	Relation type
CASP1P1	TF binding region
CARD18	TF binding region
CASP1P1	CpG island
CARD18	CpG island

Extended variants
information (count: 1444 )
Associated
traits (count: 95 )

Variant overlapped rSNPs/rCNVs (count:1444 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs552956229	chr11:104995008-104995009	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs566351221	chr11:104995027-104995028	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs113629945	chr11:104995044-104995045	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs558264964	chr11:104995121-104995122	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs138621838	chr11:104995192-104995193	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs565830527	chr11:104995209-104995210	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs371861193	chr11:104995211-104995212	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs543916469	chr11:104995255-104995256	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs544237482	chr11:104995261-104995262	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs113295492	chr11:104995295-104995296	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs534235982	chr11:104995302-104995303	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs543322462	chr11:104995371-104995372	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs142905059	chr11:104995404-104995405	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs147008454	chr11:104995414-104995415	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs77700782	chr11:104995446-104995447	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs565420269	chr11:104995465-104995466	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs71484396	chr11:104995480-104995481	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs531031796	chr11:104995528-104995529	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs189010371	chr11:104995531-104995532	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs372908731	chr11:104995587-104995588	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs530013801	chr11:104995637-104995638	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs191927001	chr11:104995670-104995671	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs79628999	chr11:104995672-104995673	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs111740764	chr11:104995675-104995676	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs184881606	chr11:104995680-104995681	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs369637825	chr11:104995683-104995684	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs138054654	chr11:104995687-104995688	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs537954041	chr11:104995749-104995750	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs554334953	chr11:104995782-104995783	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs574397343	chr11:104995787-104995788	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs149505496	chr11:104995789-104995790	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs553740007	chr11:104995815-104995816	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs117984560	chr11:104995884-104995885	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs545664722	chr11:104995924-104995925	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs542070919	chr11:104995928-104995929	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs144299755	chr11:104995949-104995950	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs189194240	chr11:104995978-104995979	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs561202333	chr11:104996000-104996001	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs34692504	chr11:104996020-104996021	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs386757125	chr11:104996022-104996023	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs373311360	chr11:104996023-104996024	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs560060403	chr11:104996024-104996025	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs1503390	chr11:104996037-104996038	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs180719340	chr11:104996063-104996064	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs569047891	chr11:104996064-104996065	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs538848771	chr11:104996142-104996143	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs187235587	chr11:104996165-104996166	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs148749174	chr11:104996196-104996197	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs142004510	chr11:104996202-104996203	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs552195812	chr11:104996214-104996215	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:95)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Gastric cancer	17908304	CNVD
Multiple myeloma	20724749	CNVD
Wilms tumour	21544195	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Acute myeloid leukemia	20729466	CNVD
Cancer	21637783	CNVD
Acute myeloid leukemia	16864856	CNVD
Chronic lymphocytic leukemia	21795749	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	21484798	CNVD
Ewing''s sarcoma	21437220	CNVD
Oral cancer	21386901	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	20837533	CNVD
Breast cancer	21264507	CNVD
Cervical cancer	21063398	CNVD
Glioblastoma multiforme	19960244	CNVD
Liposarcoma	21253554	CNVD
Neuroblastoma	18923524	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Neuroblastoma	17533364	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Glioblastoma multiforme	21080181	CNVD
Cancer	16751803	CNVD
Seminomas	18059402	CNVD
Cervical cancer	21062161	CNVD
Esophageal squamous carcinoma	18350619	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Neuroblastoma	18923191	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	22429812	CNVD
Breast cancer	16608533	CNVD
T-cell lymphomas	19863542	CNVD
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Basal cell lymphoma	17053054	CNVD
Hepatocellular carcinoma	16785998	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	21858162	CNVD
Breast cancer	21785460	CNVD
Breast cancer	21958427	CNVD
Lung cancer	18438408	CNVD
Ewing''s sarcoma	17952124	CNVD
Renal cell carcinoma	18194544	CNVD
Breast cancer	17133270	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	17603634	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Basal cell lymphoma	16790693	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Breast cancer	21364760	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Mental retardation	19966786	CNVD
Non-small cell lung cancer	21829676	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Intracranial aneurysm	16715129	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Urothelial carcinoma	21177765	CNVD
Myelofibrosis	22110671	CNVD
Ovarian cancer	21720365	CNVD
Chronic lymphocytic leukemia	17805327	CNVD
Glioblastoma multiforme	22286061	CNVD
Breast cancer	16397240	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Neuroblastoma	17327916	CNVD
Melanoma	17363583	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Esophageal squamous carcinoma	17470683	CNVD
Mantle cell lymphoma	19029149	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Malignant melanoma	17260012	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Prostate cancer	16573809	CNVD
Obesity	19966786	CNVD
Prostate cancer	18632612	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Schizophrenia	23813976	CNVD

Chromatin state (count:105 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:104995000-104995400	Enhancers	Fetal Heart	heart
2	chr11:104995200-104997000	Enhancers	Placenta	Placenta
3	chr11:104997000-105000800	Weak transcription	Placenta	Placenta
4	chr11:104997400-105000800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr11:105000800-105001600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
6	chr11:105000800-105001600	Enhancers	NHEK	skin
7	chr11:105000800-105001800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
8	chr11:105000800-105001800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
9	chr11:105000800-105002000	Enhancers	HMEC	breast
10	chr11:105000800-105002200	Enhancers	Placenta	Placenta
11	chr11:105001000-105001600	Enhancers	Esophagus	oesophagus
12	chr11:105001200-105001600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
13	chr11:105001400-105001600	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
14	chr11:105001400-105001600	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
15	chr11:105001600-105001800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
16	chr11:105001800-105002400	ZNF genes & repeats	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
17	chr11:105002000-105002200	ZNF genes & repeats	HMEC	breast
18	chr11:105002200-105003600	Weak transcription	HMEC	breast
19	chr11:105002400-105002800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
20	chr11:105002400-105008000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
21	chr11:105003200-105003400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
22	chr11:105003400-105004200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
23	chr11:105003600-105004400	Enhancers	HMEC	breast
24	chr11:105003600-105004600	Enhancers	HUVEC	blood vessel
25	chr11:105003800-105004600	Enhancers	NHEK	skin
26	chr11:105004200-105004800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
27	chr11:105004200-105005200	Enhancers	Hela-S3	cervix
28	chr11:105004400-105007600	Weak transcription	HMEC	breast
29	chr11:105004600-105007600	Weak transcription	HUVEC	blood vessel
30	chr11:105004800-105007800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
31	chr11:105007200-105008800	Enhancers	Fetal Heart	heart
32	chr11:105007600-105008400	Enhancers	HUVEC	blood vessel
33	chr11:105007600-105008600	Enhancers	HMEC	breast
34	chr11:105007600-105009000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
35	chr11:105007600-105010600	Enhancers	NHEK	skin
36	chr11:105007800-105010600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
37	chr11:105008000-105008400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
38	chr11:105008000-105010600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
39	chr11:105008000-105011200	Enhancers	Breast Myoepithelial Primary Cells	Breast
40	chr11:105008200-105008600	Enhancers	Placenta Amnion	Placenta Amnion
41	chr11:105008400-105012000	Weak transcription	HUVEC	blood vessel
42	chr11:105008600-105009600	Weak transcription	HMEC	breast
43	chr11:105009000-105010000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
44	chr11:105009600-105010800	Enhancers	HMEC	breast
45	chr11:105010000-105010600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
46	chr11:105010600-105015600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
47	chr11:105010600-105015600	Weak transcription	NHEK	skin
48	chr11:105010600-105026400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
49	chr11:105010800-105015200	Weak transcription	HMEC	breast
50	chr11:105011200-105012600	Weak transcription	Breast Myoepithelial Primary Cells	Breast

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