Variant report

Variant	nsv888934
Chromosome Location	chr7:105016900-105056010
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1199)
CpG islands
(count:795)
Chromatin interactive
region (count:53)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1199 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:105017364-105017690	K562	blood:	n/a	n/a
2	ARID3A	chr7:105019839-105020013	K562	blood:	n/a	n/a
3	ARID3A	chr7:105039898-105040131	HepG2	liver:	n/a	n/a
4	ARID3A	chr7:105039651-105040180	K562	blood:	n/a	n/a
5	ARID3A	chr7:105028117-105028318	K562	blood:	n/a	n/a
6	ARID3A	chr7:105042910-105043317	K562	blood:	n/a	n/a
7	ARID3A	chr7:105042035-105042531	K562	blood:	n/a	n/a
8	ARID3A	chr7:105042094-105042482	HepG2	liver:	n/a	n/a
9	ARID3A	chr7:105029792-105030248	HepG2	liver:	n/a	n/a
10	BACH1	chr7:105027844-105028042	K562	blood:	n/a	n/a
11	BACH1	chr7:105028171-105028753	H1-hESC	embryonic stem cell:	n/a	n/a
12	BACH1	chr7:105029716-105030051	H1-hESC	embryonic stem cell:	n/a	n/a
13	BACH1	chr7:105029014-105029308	H1-hESC	embryonic stem cell:	n/a	n/a
14	BACH1	chr7:105042903-105043365	K562	blood:	n/a	n/a
15	BATF	chr7:105041762-105041974	GM12878	blood:	n/a	n/a
16	BHLHE40	chr7:105042095-105042394	K562	blood:	n/a	n/a
17	BHLHE40	chr7:105029124-105029187	K562	blood:	n/a	n/a
18	BHLHE40	chr7:105028285-105028701	K562	blood:	n/a	chr7:105028425-105028441
19	BHLHE40	chr7:105028352-105028581	GM12878	blood:	n/a	chr7:105028425-105028441
20	BHLHE40	chr7:105039812-105040017	K562	blood:	n/a	n/a
21	BHLHE40	chr7:105029661-105030115	K562	blood:	n/a	chr7:105029666-105029682
22	BHLHE40	chr7:105029678-105029984	GM12878	blood:	n/a	n/a
23	BRCA1	chr7:105029780-105029800	GM12878	blood:	n/a	n/a
24	BRCA1	chr7:105029695-105029834	HepG2	liver:	n/a	n/a
25	CBX3	chr7:105034985-105035371	K562	blood:	n/a	n/a
26	CBX3	chr7:105042025-105042557	HCT-116	colon:	n/a	n/a
27	CBX3	chr7:105041976-105042503	K562	blood:	n/a	n/a
28	CCNT2	chr7:105042201-105042473	K562	blood:	n/a	n/a
29	CCNT2	chr7:105028142-105029984	K562	blood:	n/a	chr7:105028594-105028603 chr7:105029564-105029573
30	CCNT2	chr7:105017418-105017671	K562	blood:	n/a	n/a
31	CEBPB	chr7:105044964-105045256	K562	blood:	n/a	n/a
32	CEBPB	chr7:105036900-105037090	K562	blood:	n/a	chr7:105037028-105037039
33	CEBPB	chr7:105038862-105038911	A549	lung:	n/a	n/a
34	CEBPB	chr7:105044883-105045254	K562	blood:	n/a	n/a
35	CEBPB	chr7:105025282-105025464	K562	blood:	n/a	n/a
36	CEBPB	chr7:105030782-105031053	K562	blood:	n/a	n/a
37	CEBPB	chr7:105053175-105053408	K562	blood:	n/a	chr7:105053313-105053324 chr7:105053313-105053326 chr7:105053315-105053324 chr7:105053313-105053326
38	CEBPB	chr7:105030888-105030982	A549	lung:	n/a	n/a
39	CEBPB	chr7:105038777-105038927	K562	blood:	n/a	n/a
40	CEBPB	chr7:105039451-105039665	IMR90	lung:	n/a	n/a
41	CEBPB	chr7:105038853-105038916	H1-hESC	embryonic stem cell:	n/a	n/a
42	CEBPB	chr7:105036912-105037085	HepG2	liver:	n/a	chr7:105037028-105037039
43	CHD1	chr7:105029068-105029333	GM12878	blood:	n/a	n/a
44	CHD2	chr7:105028470-105029337	K562	blood:	n/a	chr7:105028809-105028816
45	CHD2	chr7:105028747-105029206	GM12878	blood:	n/a	chr7:105028809-105028816
46	CHD2	chr7:105029588-105030003	HepG2	liver:	n/a	n/a
47	CHD2	chr7:105028349-105028549	HepG2	liver:	n/a	n/a
48	CHD2	chr7:105028300-105028500	GM12878	blood:	n/a	n/a
49	CHD2	chr7:105029562-105029963	K562	blood:	n/a	n/a
50	CHD2	chr7:105029672-105030039	H1-hESC	embryonic stem cell:	n/a	n/a

(count:795 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:105018109-105018159	ECC-1	luminal epithelium:	n/a
2	chr7:105030168-105030218	GM06990	blood:	n/a
3	chr7:105018109-105018159	ECC-1	luminal epithelium:	n/a
4	chr7:105030168-105030218	GM06990	blood:	n/a
5	chr7:105018109-105018159	HIPEpiC	eye:	n/a
6	chr7:105028539-105028589	HEK293	kidney:	embryo
7	chr7:105029492-105029542	Jurkat	blood:	n/a
8	chr7:105029497-105029547	GM12891	blood:	n/a
9	chr7:105026171-105026221	NH-A	brain:	n/a
10	chr7:105029895-105029945	GM19239	blood:	n/a
11	chr7:105026171-105026221	PrEC	prostate:	n/a
12	chr7:105029485-105029535	HEEpiC	esophagus:	n/a
13	chr7:105029385-105029435	Hepatocyte	liver:	n/a
14	chr7:105027541-105027591	Jurkat	blood:	n/a
15	chr7:105027541-105027591	SKMC	muscle:	n/a
16	chr7:105029485-105029535	HCF	heart:	n/a
17	chr7:105027541-105027591	HL-60	blood:	n/a
18	chr7:105030752-105030802	NT2-D1	testis:	n/a
19	chr7:105029499-105029549	NHBE	bronchial:	n/a
20	chr7:105027541-105027591	SK-N-SH	brain:	n/a
21	chr7:105029485-105029535	CMK	blood:	n/a
22	chr7:105029895-105029945	GM12878	blood:	n/a
23	chr7:105018109-105018159	PrEC	prostate:	n/a
24	chr7:105029125-105029175	NH-A	brain:	n/a
25	chr7:105018109-105018159	PANC-1	pancreas:	n/a
26	chr7:105026171-105026221	HRPEpiC	eye:	n/a
27	chr7:105030752-105030802	HepG2	liver:	n/a
28	chr7:105029499-105029549	GM12891	blood:	n/a
29	chr7:105028539-105028589	HL-60	blood:	n/a
30	chr7:105029125-105029175	NHBE	bronchial:	n/a
31	chr7:105029385-105029435	GM12891	blood:	n/a
32	chr7:105030168-105030218	K562	blood:	n/a
33	chr7:105029125-105029175	GM12891	blood:	n/a
34	chr7:105030168-105030218	HEK293	kidney:	embryo
35	chr7:105029125-105029175	HL-60	blood:	n/a
36	chr7:105029492-105029542	AG04449	skin:	fetal
37	chr7:105028539-105028589	HRCEpiC	kidney:	n/a
38	chr7:105018109-105018159	Caco-2	colon:	n/a
39	chr7:105030168-105030218	T-47D	breast:	n/a
40	chr7:105028539-105028589	GM06990	blood:	n/a
41	chr7:105030752-105030802	SK-N-SH_RA	brain:	n/a
42	chr7:105028539-105028589	NH-A	brain:	n/a
43	chr7:105027541-105027591	HMEC	breast:	n/a
44	chr7:105030168-105030218	HEEpiC	esophagus:	n/a
45	chr7:105027541-105027591	HEK293	kidney:	embryo
46	chr7:105027541-105027591	HRCEpiC	kidney:	n/a
47	chr7:105018109-105018159	SK-N-MC	brain:	n/a
48	chr7:105029499-105029549	Jurkat	blood:	n/a
49	chr7:105030752-105030802	ProgFib	skin:	n/a
50	chr7:105030168-105030218	HMEC	breast:	n/a

(count:53 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr7:105016302..105018652-chr7:105027482..105029964,4	K562	blood:
2	chr7:104652893..104655901-chr7:105027705..105031319,8	MCF-7	breast:
3	chr7:105039769..105040575-chr7:105229933..105230493,2	MCF-7	breast:
4	chr7:105029590..105031238-chr7:105038445..105041248,2	MCF-7	breast:
5	chr7:105009408..105012962-chr7:105018316..105021525,4	K562	blood:
6	chr7:105039077..105041810-chr7:105045428..105047601,2	K562	blood:
7	chr7:105033753..105035269-chr7:105037769..105040166,2	K562	blood:
8	chr7:105030763..105032789-chr7:105035167..105036681,2	K562	blood:
9	chr7:104998364..105000069-chr7:105014709..105017668,2	K562	blood:
10	chr7:104715799..104718256-chr7:105026783..105029016,2	K562	blood:
11	chr7:104652744..104654842-chr7:105028526..105031470,2	MCF-7	breast:
12	chr7:104650837..104656019-chr7:105026206..105030997,7	K562	blood:
13	chr7:105026975..105030937-chr7:105032940..105036440,7	K562	blood:
14	chr7:105027746..105030082-chr7:105160759..105163665,5	MCF-7	breast:
15	chr7:105027932..105031943-chr7:105036648..105042469,7	K562	blood:
16	chr7:104971088..104973665-chr7:105027778..105030280,2	K562	blood:
17	chr7:105012234..105014245-chr7:105022510..105026066,3	K562	blood:
18	chr7:105029590..105031238-chr7:105038445..105041248,2	MCF-7	breast:
19	chr7:105019911..105021910-chr7:105024677..105026313,2	K562	blood:
20	chr7:105039956..105042512-chr7:105104408..105106506,2	K562	blood:
21	chr7:105030763..105032789-chr7:105035167..105036681,2	K562	blood:
22	chr7:105041786..105042328-chr7:105128303..105129103,3	MCF-7	breast:
23	chr7:105026529..105029377-chr7:105162488..105165118,2	MCF-7	breast:
24	chr5:43514739..43515249-chr7:105041985..105042577,2	Hela-S3	cervix:
25	chr7:105027873..105030289-chr7:105032532..105034391,3	MCF-7	breast:
26	chr7:104937663..104939344-chr7:105026759..105029557,2	MCF-7	breast:
27	chr7:105029252..105029910-chr9:3525726..3526715,2	NB4	blood:
28	chr5:144628686..144629379-chr7:105027367..105028166,2	MCF-7	breast:
29	chr7:104652684..104654686-chr7:105018290..105019897,2	K562	blood:
30	chr7:105012623..105015003-chr7:105017126..105018970,2	MCF-7	breast:
31	chr7:105041915..105043798-chr7:105045520..105047244,3	K562	blood:
32	chr7:104653211..104654776-chr7:105027099..105029228,2	K562	blood:
33	chr7:105027206..105036314-chr7:105036751..105044757,13	K562	blood:
34	chr7:105027206..105036314-chr7:105036751..105044757,13	K562	blood:
35	chr7:105009330..105013041-chr7:105014599..105017566,3	K562	blood:
36	chr7:105041915..105043798-chr7:105045520..105047244,3	K562	blood:
37	chr7:104651368..104653205-chr7:105026206..105027848,2	K562	blood:
38	chr7:105019571..105021474-chr7:105027326..105029018,2	MCF-7	breast:
39	chr7:105038088..105039818-chr7:105043302..105044810,2	K562	blood:
40	chr7:105019571..105021474-chr7:105027326..105029018,2	MCF-7	breast:
41	chr7:105007315..105010553-chr7:105026431..105029268,4	MCF-7	breast:
42	chr7:105041648..105042543-chr7:105069609..105070839,7	MCF-7	breast:
43	chr7:104757007..104759673-chr7:105027481..105029991,2	MCF-7	breast:
44	chr7:105027141..105031088-chr7:105032244..105036688,5	MCF-7	breast:
45	chr7:104649601..104653676-chr7:105029497..105032094,4	K562	blood:
46	chr7:105028493..105030859-chr7:105041112..105043880,2	MCF-7	breast:
47	chr7:105019911..105021910-chr7:105024677..105026313,2	K562	blood:
48	chr7:105027174..105029032-chr7:105171146..105173908,2	K562	blood:
49	chr7:105038088..105039818-chr7:105043302..105044828,3	K562	blood:
50	chr7:105028215..105030486-chr7:105171271..105172847,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SRPK2-5	chr7:105029095-105029149	NONHSAT122614
2	lnc-SRPK2-5	chr7:105029691-105029837	NONHSAT122614

No data

Variant related genes	Relation type
SRPK2	TF binding region
SRPK2	CpG island
ENSG00000201179	chromatin interactions
ENSG00000005483	chromatin interactions
ENSG00000091127	chromatin interactions
ENSG00000172244	chromatin interactions
ENSG00000135249	chromatin interactions
ENSG00000239569	chromatin interactions
ENSG00000228393	chromatin interactions
ENSG00000080298	chromatin interactions
ENSG00000135250	chromatin interactions

Extended variants
information (count: 1349 )
Associated
traits (count: 78 )

Variant overlapped rSNPs/rCNVs (count:1349 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10249417	chr7:105016900-105016901	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs148159547	chr7:105016903-105016904	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs554491052	chr7:105016911-105016912	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs144022900	chr7:105016971-105016972	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs376600508	chr7:105016982-105016983	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs535462244	chr7:105017035-105017036	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs371379731	chr7:105017049-105017050	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs183541111	chr7:105017050-105017051	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs188245483	chr7:105017091-105017092	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs543925917	chr7:105017122-105017123	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs563794932	chr7:105017129-105017130	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs577427463	chr7:105017133-105017134	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs190262253	chr7:105017134-105017135	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs560440931	chr7:105017161-105017162	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs182558387	chr7:105017230-105017231	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs186469899	chr7:105017242-105017243	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs367616245	chr7:105017263-105017264	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs549391062	chr7:105017274-105017275	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs6959826	chr7:105017276-105017277	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs191343155	chr7:105017277-105017278	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs531709323	chr7:105017279-105017280	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs28427071	chr7:105017288-105017289	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs28432056	chr7:105017289-105017290	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs553070871	chr7:105017290-105017291	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs28508115	chr7:105017295-105017296	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs35855824	chr7:105017296-105017297	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs34080086	chr7:105017329-105017330	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs374460062	chr7:105017330-105017331	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs71152967	chr7:105017349-105017350	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs551907111	chr7:105017354-105017355	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs397935916	chr7:105017357-105017358	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs76799177	chr7:105017492-105017493	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs138060361	chr7:105017523-105017524	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs547654939	chr7:105017530-105017531	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs376674537	chr7:105017544-105017545	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs76849218	chr7:105017567-105017568	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs536562138	chr7:105017569-105017570	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs201814258	chr7:105017583-105017584	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs143527620	chr7:105017586-105017587	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs574899135	chr7:105017614-105017615	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs76740650	chr7:105017639-105017640	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs557467910	chr7:105017698-105017699	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs577590285	chr7:105017709-105017710	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs577312100	chr7:105017834-105017835	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs544633350	chr7:105017854-105017855	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs566285308	chr7:105017862-105017863	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs570057649	chr7:105017864-105017865	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs560071448	chr7:105017899-105017900	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs575444358	chr7:105017905-105017906	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs113474944	chr7:105017977-105017978	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:78)

Disease	PMID	Source
Basal cell lymphoma	17170743	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Thyroid cancer	19087340	CNVD
Seminomas	18059402	CNVD
Testicular cancer	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	19415332	CNVD
Medulloblastoma	21979893	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
T-cell lymphomas	19863542	CNVD
Malaria	21533027	CNVD
Melanoma	18172304	CNVD
Renal cell carcinoma	19461508	CNVD
head and neck squamous cell carcinoma	19289630	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
Non-small cell lung cancer	21829676	CNVD
Glioblastoma multiforme	17002787	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Lissencephaly	21572526	CNVD
Breast cancer	17603634	CNVD
Liposarcoma	21253554	CNVD
Breast cancer	16397240	CNVD
Acute myeloid leukemia	16864856	CNVD
Squamous cell cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Astrocytoma	17387387	CNVD
Glioblastoma multiforme	17387387	CNVD
Low-grade fibromyxoid sarcoma	0	CNVD
Oligodendroglial tumors	17285580	CNVD
Endometrial cancer	22040021	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	21264507	CNVD
Shwachman-Diamond syndrome	22934832	CNVD
Colorectal cancer	19359472	CNVD
Cutaneous malignant melanoma	17690212	CNVD
Leukemia	17361228	CNVD
Breast cancer	16461572	CNVD
Peripheral t-cell lymphoma	19118030	CNVD
Malignant melanoma	17690212	CNVD
Renal cell carcinoma	18592004	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Multiple myeloma	17550852	CNVD
small cell lung cancer	20016488	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Neurodevelopmental disorder	22521361	CNVD
abortions and stillbirths	19751515	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Acute myeloid leukemia	20729466	CNVD
Lung cancer	18438408	CNVD
Metanephric adenoma	20802469	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Burkitt''s lymphoma	19759907	CNVD
Malignant melanoma	17260012	CNVD
Myelodysplastic syndrome	21251322	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	21785460	CNVD
Chronic myeloid leukemia	21384125	CNVD
Breast cancer	21858162	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Autism	19401682	CNVD
Neuroticism	17667963	CNVD
Prostate cancer	18632612	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Breast cancer	21364760	CNVD
lymphocytic leukemia	21291569	CNVD
Basal cell lymphoma	17053054	CNVD
Myelofibrosis	22110671	CNVD
Prostate cancer	16573809	CNVD
Myxofibrosarcoma	20639860	CNVD
Pancreatic cancer	17952125	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:733 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:104995200-105028200	Weak transcription	Esophagus	oesophagus
2	chr7:104995400-105028000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
3	chr7:104995600-105027200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
4	chr7:104995800-105027200	Weak transcription	Primary T cells from cord blood	blood
5	chr7:104996400-105017000	Weak transcription	Fetal Muscle Leg	muscle
6	chr7:104997400-105026800	Weak transcription	Primary B cells from cord blood	blood
7	chr7:105000000-105018000	Weak transcription	Lung	lung
8	chr7:105000000-105021800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
9	chr7:105000000-105028200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
10	chr7:105000200-105025800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
11	chr7:105003200-105027600	Weak transcription	Fetal Intestine Small	intestine
12	chr7:105003600-105025200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
13	chr7:105005000-105021200	Weak transcription	Fetal Stomach	stomach
14	chr7:105006200-105017400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
15	chr7:105006200-105027600	Weak transcription	Hela-S3	cervix
16	chr7:105006400-105021400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
17	chr7:105006400-105027400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
18	chr7:105008000-105017600	Weak transcription	Gastric	stomach
19	chr7:105008200-105028200	Weak transcription	Pancreas	Pancrea
20	chr7:105009200-105018600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
21	chr7:105009200-105027200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
22	chr7:105009200-105028000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
23	chr7:105009200-105028000	Weak transcription	Psoas Muscle	Psoas
24	chr7:105009600-105018000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
25	chr7:105010000-105017400	Weak transcription	Primary B cells from peripheral blood	blood
26	chr7:105010000-105027400	Weak transcription	Muscle Satellite Cultured Cells	--
27	chr7:105010800-105017600	Weak transcription	Sigmoid Colon	Sigmoid Colon
28	chr7:105011400-105017800	Weak transcription	Primary T cells fromperipheralblood	blood
29	chr7:105012200-105017400	Weak transcription	HepG2	liver
30	chr7:105015200-105017000	Enhancers	Primary T helper cells PMA-I stimulated	--
31	chr7:105015400-105017400	Weak transcription	HUES48 Cell Line	embryonic stem cell
32	chr7:105015800-105017000	Enhancers	Primary T helper naive cells fromperipheralblood	blood
33	chr7:105015800-105017400	Enhancers	K562	blood
34	chr7:105015800-105018800	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
35	chr7:105016000-105017400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
36	chr7:105016000-105017600	Weak transcription	Ovary	ovary
37	chr7:105016200-105017400	Weak transcription	A549	lung
38	chr7:105016200-105018000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
39	chr7:105016200-105025800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
40	chr7:105016200-105026200	Weak transcription	Dnd41	blood
41	chr7:105016400-105017800	Weak transcription	Primary T helper cells fromperipheralblood	blood
42	chr7:105016400-105027000	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
43	chr7:105016400-105027200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
44	chr7:105017000-105017600	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
45	chr7:105017000-105017600	Weak transcription	Primary T helper cells PMA-I stimulated	--
46	chr7:105017000-105017800	Enhancers	Fetal Muscle Leg	muscle
47	chr7:105017400-105017600	Enhancers	iPS-15b Cell Line	embryonic stem cell
48	chr7:105017400-105017600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
49	chr7:105017400-105017800	Enhancers	Primary B cells from peripheral blood	blood
50	chr7:105017400-105017800	Enhancers	A549	lung

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