Variant report

Variant	esv3436858
Chromosome Location	chr7:105017550-105044209
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1128)
CpG islands
(count:794)
Chromatin interactive
region (count:51)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1128 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:105028117-105028318	K562	blood:	n/a	n/a
2	ARID3A	chr7:105039651-105040180	K562	blood:	n/a	n/a
3	ARID3A	chr7:105042910-105043317	K562	blood:	n/a	n/a
4	ARID3A	chr7:105039898-105040131	HepG2	liver:	n/a	n/a
5	ARID3A	chr7:105042035-105042531	K562	blood:	n/a	n/a
6	ARID3A	chr7:105029792-105030248	HepG2	liver:	n/a	n/a
7	ARID3A	chr7:105017364-105017690	K562	blood:	n/a	n/a
8	ARID3A	chr7:105019839-105020013	K562	blood:	n/a	n/a
9	ARID3A	chr7:105042094-105042482	HepG2	liver:	n/a	n/a
10	BACH1	chr7:105042903-105043365	K562	blood:	n/a	n/a
11	BACH1	chr7:105028171-105028753	H1-hESC	embryonic stem cell:	n/a	n/a
12	BACH1	chr7:105027844-105028042	K562	blood:	n/a	n/a
13	BACH1	chr7:105029014-105029308	H1-hESC	embryonic stem cell:	n/a	n/a
14	BACH1	chr7:105029716-105030051	H1-hESC	embryonic stem cell:	n/a	n/a
15	BATF	chr7:105041762-105041974	GM12878	blood:	n/a	n/a
16	BHLHE40	chr7:105029678-105029984	GM12878	blood:	n/a	n/a
17	BHLHE40	chr7:105029661-105030115	K562	blood:	n/a	chr7:105029666-105029682
18	BHLHE40	chr7:105028352-105028581	GM12878	blood:	n/a	chr7:105028425-105028441
19	BHLHE40	chr7:105028285-105028701	K562	blood:	n/a	chr7:105028425-105028441
20	BHLHE40	chr7:105029124-105029187	K562	blood:	n/a	n/a
21	BHLHE40	chr7:105039812-105040017	K562	blood:	n/a	n/a
22	BHLHE40	chr7:105042095-105042394	K562	blood:	n/a	n/a
23	BRCA1	chr7:105029695-105029834	HepG2	liver:	n/a	n/a
24	BRCA1	chr7:105029780-105029800	GM12878	blood:	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	chr7:105039451-105039665	IMR90	lung:	n/a	n/a
32	CEBPB	chr7:105036900-105037090	K562	blood:	n/a	chr7:105037028-105037039
33	CEBPB	chr7:105030782-105031053	K562	blood:	n/a	n/a
34	CEBPB	chr7:105038862-105038911	A549	lung:	n/a	n/a
35	CEBPB	chr7:105038853-105038916	H1-hESC	embryonic stem cell:	n/a	n/a
36	CEBPB	chr7:105025282-105025464	K562	blood:	n/a	n/a
37	CEBPB	chr7:105030888-105030982	A549	lung:	n/a	n/a
38	CEBPB	chr7:105038777-105038927	K562	blood:	n/a	n/a
39	CEBPB	chr7:105036912-105037085	HepG2	liver:	n/a	chr7:105037028-105037039
40	CHD1	chr7:105029068-105029333	GM12878	blood:	n/a	n/a
41	CHD2	chr7:105029672-105030039	H1-hESC	embryonic stem cell:	n/a	n/a
42	CHD2	chr7:105028747-105029206	GM12878	blood:	n/a	chr7:105028809-105028816
43	CHD2	chr7:105028470-105029337	K562	blood:	n/a	chr7:105028809-105028816
44	CHD2	chr7:105029054-105029301	HepG2	liver:	n/a	n/a
45	CHD2	chr7:105028349-105028549	HepG2	liver:	n/a	n/a
46	CHD2	chr7:105029647-105029883	GM12878	blood:	n/a	n/a
47	CHD2	chr7:105028537-105029884	Hela-S3	cervix:	n/a	chr7:105028809-105028816
48	CHD2	chr7:105028531-105028711	H1-hESC	embryonic stem cell:	n/a	n/a
49	CHD2	chr7:105029562-105029963	K562	blood:	n/a	n/a
50	CHD2	chr7:105029588-105030003	HepG2	liver:	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	chr7:105029485-105029535	HRPEpiC	eye:	n/a
2	chr7:105029485-105029535	HRPEpiC	eye:	n/a
3	chr7:105018109-105018159	T-47D	breast:	n/a
4	chr7:105029492-105029542	HUVEC	blood vessel:	n/a
5	chr7:105029385-105029435	AG04450	lung:	fetal
6	chr7:105028539-105028589	ECC-1	luminal epithelium:	n/a
7	chr7:105029385-105029435	HEEpiC	esophagus:	n/a
8	chr7:105030752-105030802	HEK293	kidney:	embryo
9	chr7:105028539-105028589	GM19239	blood:	n/a
10	chr7:105029895-105029945	PrEC	prostate:	n/a
11	chr7:105018109-105018159	BJ	skin:	n/a
12	chr7:105029895-105029945	AG04450	lung:	fetal
13	chr7:105027541-105027591	Caco-2	colon:	n/a
14	chr7:105029499-105029549	Hepatocyte	liver:	n/a
15	chr7:105029895-105029945	Jurkat	blood:	n/a
16	chr7:105029497-105029547	HL-60	blood:	n/a
17	chr7:105029895-105029945	SK-N-SH_RA	brain:	n/a
18	chr7:105029499-105029549	MCF-7	breast:	n/a
19	chr7:105030168-105030218	HNPCEpiC	eye:	n/a
20	chr7:105029492-105029542	HEEpiC	esophagus:	n/a
21	chr7:105029499-105029549	Caco-2	colon:	n/a
22	chr7:105029385-105029435	NHDF-neo	bronchial:	n/a
23	chr7:105029385-105029435	CMK	blood:	n/a
24	chr7:105026171-105026221	HNPCEpiC	eye:	n/a
25	chr7:105029485-105029535	GM12891	blood:	n/a
26	chr7:105029895-105029945	AG09309	skin:	n/a
27	chr7:105029499-105029549	MCF10A-Er-Src	breast:	n/a
28	chr7:105029485-105029535	HRCEpiC	kidney:	n/a
29	chr7:105018109-105018159	ECC-1	luminal epithelium:	n/a
30	chr7:105028539-105028589	HCF	heart:	n/a
31	chr7:105029492-105029542	NB4	blood:	n/a
32	chr7:105029499-105029549	SK-N-SH	brain:	n/a
33	chr7:105029499-105029549	NHBE	bronchial:	n/a
34	chr7:105029125-105029175	HCF	heart:	n/a
35	chr7:105029385-105029435	NH-A	brain:	n/a
36	chr7:105018109-105018159	AG10803	skin:	n/a
37	chr7:105029125-105029175	RPTEC	kidney:	n/a
38	chr7:105029497-105029547	HCF	heart:	n/a
39	chr7:105029497-105029547	BJ	skin:	n/a
40	chr7:105029497-105029547	SKMC	muscle:	n/a
41	chr7:105026171-105026221	K562	blood:	n/a
42	chr7:105018109-105018159	NHBE	bronchial:	n/a
43	chr7:105029499-105029549	AG04449	skin:	fetal
44	chr7:105029895-105029945	BJ	skin:	n/a
45	chr7:105029125-105029175	AG04449	skin:	fetal
46	chr7:105030168-105030218	HRCEpiC	kidney:	n/a
47	chr7:105029125-105029175	MCF-7	breast:	n/a
48	chr7:105029385-105029435	SK-N-SH_RA	brain:	n/a
49	chr7:105029895-105029945	GM12878	blood:	n/a
50	chr7:105030168-105030218	NB4	blood:	n/a

(count:51 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr7:105027206..105036314-chr7:105036751..105044757,13	K562	blood:
2	chr7:105009330..105013041-chr7:105014599..105017566,3	K562	blood:
3	chr7:105038088..105039818-chr7:105043302..105044810,2	K562	blood:
4	chr7:105029590..105031238-chr7:105038445..105041248,2	MCF-7	breast:
5	chr7:104649601..104653676-chr7:105029497..105032094,4	K562	blood:
6	chr7:105027746..105030082-chr7:105160759..105163665,5	MCF-7	breast:
7	chr7:105039956..105042512-chr7:105104408..105106506,2	K562	blood:
8	chr7:105028493..105030859-chr7:105041112..105043880,2	MCF-7	breast:
9	chr7:104937663..104939344-chr7:105026759..105029557,2	MCF-7	breast:
10	chr7:105024723..105026503-chr7:105037837..105040106,2	K562	blood:
11	chr7:104652893..104655901-chr7:105027705..105031319,8	MCF-7	breast:
12	chr7:105027932..105031943-chr7:105036648..105042469,7	K562	blood:
13	chr7:105041648..105042543-chr7:105069609..105070839,7	MCF-7	breast:
14	chr7:105012234..105014245-chr7:105022510..105026066,3	K562	blood:
15	chr7:105012623..105015003-chr7:105017126..105018970,2	MCF-7	breast:
16	chr7:105041786..105042328-chr7:105128303..105129103,3	MCF-7	breast:
17	chr7:104650837..104656019-chr7:105026206..105030997,7	K562	blood:
18	chr7:104652744..104654842-chr7:105028526..105031470,2	MCF-7	breast:
19	chr7:105041915..105043798-chr7:105045520..105047244,3	K562	blood:
20	chr7:105027873..105030289-chr7:105032532..105034391,3	MCF-7	breast:
21	chr7:105019571..105021474-chr7:105027326..105029018,2	MCF-7	breast:
22	chr7:105029590..105031238-chr7:105038445..105041248,2	MCF-7	breast:
23	chr7:105027141..105031088-chr7:105032244..105036688,5	MCF-7	breast:
24	chr7:105009408..105012962-chr7:105018316..105021525,4	K562	blood:
25	chr7:104757007..104759673-chr7:105027481..105029991,2	MCF-7	breast:
26	chr7:104651368..104653205-chr7:105026206..105027848,2	K562	blood:
27	chr7:105029252..105029910-chr9:3525726..3526715,2	NB4	blood:
28	chr7:104971088..104973665-chr7:105027778..105030280,2	K562	blood:
29	chr7:104653578..104656991-chr7:105040264..105042441,3	MCF-7	breast:
30	chr5:43514739..43515249-chr7:105041985..105042577,2	Hela-S3	cervix:
31	chr7:105030763..105032789-chr7:105035167..105036681,2	K562	blood:
32	chr7:105027174..105029032-chr7:105171146..105173908,2	K562	blood:
33	chr7:105026975..105030937-chr7:105032940..105036440,7	K562	blood:
34	chr7:105019911..105021910-chr7:105024677..105026313,2	K562	blood:
35	chr7:104715799..104718256-chr7:105026783..105029016,2	K562	blood:
36	chr7:105019911..105021910-chr7:105024677..105026313,2	K562	blood:
37	chr7:104652684..104654686-chr7:105018290..105019897,2	K562	blood:
38	chr7:105039769..105040575-chr7:105229933..105230493,2	MCF-7	breast:
39	chr7:105033753..105035269-chr7:105037769..105040166,2	K562	blood:
40	chr7:105038088..105039818-chr7:105043302..105044828,3	K562	blood:
41	chr7:105027206..105036314-chr7:105036751..105044757,13	K562	blood:
42	chr7:105016302..105018652-chr7:105027482..105029964,4	K562	blood:
43	chr7:105027932..105031943-chr7:105036648..105042469,7	K562	blood:
44	chr7:105028215..105030486-chr7:105171271..105172847,2	K562	blood:
45	chr7:105026529..105029377-chr7:105162488..105165118,2	MCF-7	breast:
46	chr7:104653211..104654776-chr7:105027099..105029228,2	K562	blood:
47	chr5:144628686..144629379-chr7:105027367..105028166,2	MCF-7	breast:
48	chr7:105030763..105032789-chr7:105035167..105036681,2	K562	blood:
49	chr7:104998364..105000069-chr7:105014709..105017668,2	K562	blood:
50	chr7:105019571..105021474-chr7:105027326..105029018,2	MCF-7	breast:

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

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

No data

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

Extended variants
information (count: 1077 )
Associated
traits (count: 78 )

Variant overlapped rSNPs/rCNVs (count:1077 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs76849218	chr7:105017567-105017568	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs536562138	chr7:105017569-105017570	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs201814258	chr7:105017583-105017584	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs143527620	chr7:105017586-105017587	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs574899135	chr7:105017614-105017615	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs76740650	chr7:105017639-105017640	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs557467910	chr7:105017698-105017699	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs577590285	chr7:105017709-105017710	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs577312100	chr7:105017834-105017835	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs544633350	chr7:105017854-105017855	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs566285308	chr7:105017862-105017863	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs570057649	chr7:105017864-105017865	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs560071448	chr7:105017899-105017900	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs575444358	chr7:105017905-105017906	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs113474944	chr7:105017977-105017978	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs577025613	chr7:105017978-105017979	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs377287043	chr7:105017979-105017980	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs542577439	chr7:105018034-105018035	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs560732726	chr7:105018049-105018050	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs377063634	chr7:105018103-105018104	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs369627061	chr7:105018122-105018123	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs566533667	chr7:105018147-105018148	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs562724650	chr7:105018202-105018203	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs77563845	chr7:105018231-105018232	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs551797950	chr7:105018240-105018241	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs117685567	chr7:105018244-105018245	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs528233615	chr7:105018265-105018266	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs562036498	chr7:105018270-105018271	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs547837185	chr7:105018272-105018273	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs117151986	chr7:105018273-105018274	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs536808160	chr7:105018439-105018440	Enhancers Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
32	rs541147074	chr7:105018444-105018445	Enhancers Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
33	rs560940204	chr7:105018462-105018463	Enhancers Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
34	rs570008041	chr7:105018476-105018477	Enhancers Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
35	rs537490952	chr7:105018592-105018593	Enhancers Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
36	rs185628487	chr7:105018609-105018610	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
37	rs571041978	chr7:105018616-105018617	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
38	rs67678290	chr7:105018663-105018664	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs372749025	chr7:105018664-105018665	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs76975839	chr7:105018679-105018680	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs79863941	chr7:105018680-105018681	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs533374486	chr7:105018714-105018715	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs533665290	chr7:105018737-105018738	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs188892429	chr7:105018801-105018802	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs144635854	chr7:105018811-105018812	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs531518399	chr7:105018830-105018831	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs193153038	chr7:105018835-105018836	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs551478063	chr7:105018853-105018854	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs576383582	chr7:105018870-105018871	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs545454178	chr7:105018960-105018961	Weak transcription	Chromatin interactive region	3 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:717 , 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	chr7:104997400-105026800	Weak transcription	Primary B cells from cord blood	blood
6	chr7:105000000-105018000	Weak transcription	Lung	lung
7	chr7:105000000-105021800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
8	chr7:105000000-105028200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
9	chr7:105000200-105025800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
10	chr7:105003200-105027600	Weak transcription	Fetal Intestine Small	intestine
11	chr7:105003600-105025200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
12	chr7:105005000-105021200	Weak transcription	Fetal Stomach	stomach
13	chr7:105006200-105027600	Weak transcription	Hela-S3	cervix
14	chr7:105006400-105021400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
15	chr7:105006400-105027400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
16	chr7:105008000-105017600	Weak transcription	Gastric	stomach
17	chr7:105008200-105028200	Weak transcription	Pancreas	Pancrea
18	chr7:105009200-105018600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
19	chr7:105009200-105027200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
20	chr7:105009200-105028000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
21	chr7:105009200-105028000	Weak transcription	Psoas Muscle	Psoas
22	chr7:105009600-105018000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
23	chr7:105010000-105027400	Weak transcription	Muscle Satellite Cultured Cells	--
24	chr7:105010800-105017600	Weak transcription	Sigmoid Colon	Sigmoid Colon
25	chr7:105011400-105017800	Weak transcription	Primary T cells fromperipheralblood	blood
26	chr7:105015800-105018800	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
27	chr7:105016000-105017600	Weak transcription	Ovary	ovary
28	chr7:105016200-105018000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
29	chr7:105016200-105025800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
30	chr7:105016200-105026200	Weak transcription	Dnd41	blood
31	chr7:105016400-105017800	Weak transcription	Primary T helper cells fromperipheralblood	blood
32	chr7:105016400-105027000	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
33	chr7:105016400-105027200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
34	chr7:105017000-105017600	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
35	chr7:105017000-105017600	Weak transcription	Primary T helper cells PMA-I stimulated	--
36	chr7:105017000-105017800	Enhancers	Fetal Muscle Leg	muscle
37	chr7:105017400-105017600	Enhancers	iPS-15b Cell Line	embryonic stem cell
38	chr7:105017400-105017600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
39	chr7:105017400-105017800	Enhancers	Primary B cells from peripheral blood	blood
40	chr7:105017400-105017800	Enhancers	A549	lung
41	chr7:105017400-105017800	Enhancers	HepG2	liver
42	chr7:105017400-105017800	Flanking Active TSS	K562	blood
43	chr7:105017400-105018400	Enhancers	HUES64 Cell Line	embryonic stem cell
44	chr7:105017400-105018400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
45	chr7:105017400-105018600	Enhancers	ES-I3 Cell Line	embryonic stem cell
46	chr7:105017400-105018600	Enhancers	H1 Cell Line	embryonic stem cell
47	chr7:105017400-105018600	Enhancers	H9 Cell Line	embryonic stem cell
48	chr7:105017400-105018600	Enhancers	HUES48 Cell Line	embryonic stem cell
49	chr7:105017400-105018600	Enhancers	HUES6 Cell Line	embryonic stem cell
50	chr7:105017400-105018600	Enhancers	iPS-20b Cell Line	embryonic stem cell

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