Variant report

Variant	nsv888940
Chromosome Location	chr7:107210383-107229618
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:761)
CpG islands
(count:1039)
Chromatin interactive
region (count:33)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:761 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:107214069-107214179	K562	blood:	n/a	n/a
2	ARID3A	chr7:107220972-107222372	K562	blood:	n/a	n/a
3	ARID3A	chr7:107220275-107220630	K562	blood:	n/a	n/a
4	ARID3A	chr7:107220484-107220694	HepG2	liver:	n/a	n/a
5	ATF1	chr7:107220165-107221087	K562	blood:	n/a	n/a
6	ATF2	chr7:107220309-107220851	GM12878	blood:	n/a	n/a
7	ATF3	chr7:107220283-107221108	K562	blood:	n/a	n/a
8	BACH1	chr7:107220155-107220366	K562	blood:	n/a	n/a
9	BACH1	chr7:107220484-107221181	H1-hESC	embryonic stem cell:	n/a	n/a
10	BCL3	chr7:107220236-107220948	GM12878	blood:	n/a	chr7:107220398-107220411 chr7:107220785-107220794 chr7:107220622-107220635 chr7:107220671-107220684
11	BCL3	chr7:107219957-107220571	A549	lung:	n/a	chr7:107220398-107220411
12	BCL3	chr7:107220018-107220803	A549	lung:	n/a	chr7:107220398-107220411 chr7:107220785-107220794 chr7:107220622-107220635 chr7:107220671-107220684
13	BCLAF1	chr7:107220355-107220916	GM12878	blood:	n/a	chr7:107220398-107220411 chr7:107220785-107220794 chr7:107220622-107220635 chr7:107220671-107220684
14	BCLAF1	chr7:107219873-107221326	K562	blood:	n/a	chr7:107220398-107220411 chr7:107220785-107220794 chr7:107220622-107220635 chr7:107220671-107220684
15	BHLHE40	chr7:107220120-107221211	K562	blood:	n/a	chr7:107220399-107220415 chr7:107220666-107220682
16	BHLHE40	chr7:107220430-107221177	GM12878	blood:	n/a	chr7:107220666-107220682
17	BHLHE40	chr7:107221584-107221652	K562	blood:	n/a	n/a
18	BRCA1	chr7:107212028-107212047	GM12878	blood:	n/a	n/a
19	BRCA1	chr7:107221839-107222295	Hela-S3	cervix:	n/a	n/a
20	BRCA1	chr7:107220078-107220219	H1-hESC	embryonic stem cell:	n/a	n/a
21	BRCA1	chr7:107220080-107221406	Hela-S3	cervix:	n/a	n/a
22	BRCA1	chr7:107220255-107220601	HepG2	liver:	n/a	n/a
23	CBX3	chr7:107220865-107221351	K562	blood:	n/a	n/a
24	CBX3	chr7:107220030-107220838	K562	blood:	n/a	n/a
25	CCNT2	chr7:107218123-107218194	K562	blood:	n/a	n/a
26	CCNT2	chr7:107220127-107221193	K562	blood:	n/a	chr7:107220661-107220670
27	CCNT2	chr7:107221683-107221760	K562	blood:	n/a	n/a
28	CEBPB	chr7:107221765-107222475	MCF-7	breast:	n/a	chr7:107222019-107222036
29	CEBPB	chr7:107221952-107222357	A549	lung:	n/a	chr7:107222019-107222036
30	CEBPB	chr7:107219347-107219541	K562	blood:	n/a	n/a
31	CEBPB	chr7:107220049-107220454	HepG2	liver:	n/a	n/a
32	CEBPB	chr7:107220047-107221214	Hela-S3	cervix:	n/a	n/a
33	CEBPB	chr7:107221960-107222389	MCF-7	breast:	n/a	chr7:107222019-107222036
34	CEBPB	chr7:107221805-107222371	Hela-S3	cervix:	n/a	chr7:107222019-107222036
35	CEBPB	chr7:107222072-107222290	HepG2	liver:	n/a	n/a
36	CEBPB	chr7:107220071-107220394	IMR90	lung:	n/a	n/a
37	CEBPB	chr7:107221948-107222345	K562	blood:	n/a	chr7:107222019-107222036
38	CEBPB	chr7:107220055-107220575	A549	lung:	n/a	n/a
39	CEBPB	chr7:107219973-107220744	MCF-7	breast:	n/a	n/a
40	CEBPB	chr7:107220037-107221275	K562	blood:	n/a	n/a
41	CEBPB	chr7:107220182-107220344	H1-hESC	embryonic stem cell:	n/a	n/a
42	CEBPB	chr7:107220037-107220748	K562	blood:	n/a	n/a
43	CEBPB	chr7:107220919-107221188	HepG2	liver:	n/a	n/a
44	CEBPD	chr7:107220048-107221310	K562	blood:	n/a	n/a
45	CEBPD	chr7:107220441-107221132	HepG2	liver:	n/a	n/a
46	CEBPD	chr7:107220292-107221258	K562	blood:	n/a	n/a
47	CHD1	chr7:107220329-107220566	H1-hESC	embryonic stem cell:	n/a	n/a
48	CHD2	chr7:107220099-107221180	K562	blood:	n/a	n/a
49	CHD2	chr7:107222085-107222257	Hela-S3	cervix:	n/a	n/a
50	CHD2	chr7:107220493-107221126	H1-hESC	embryonic stem cell:	n/a	n/a

(count:1039 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:107221074-107221124	Jurkat	blood:	n/a
2	chr7:107220040-107220090	SK-N-SH_RA	brain:	n/a
3	chr7:107221074-107221124	Jurkat	blood:	n/a
4	chr7:107220040-107220090	SK-N-SH_RA	brain:	n/a
5	chr7:107220368-107220418	GM12878	blood:	n/a
6	chr7:107221074-107221124	SK-N-SH_RA	brain:	n/a
7	chr7:107220968-107221018	SK-N-MC	brain:	n/a
8	chr7:107223076-107223126	U87	brain:	n/a
9	chr7:107220372-107220422	A549	lung:	n/a
10	chr7:107220368-107220418	GM06990	blood:	n/a
11	chr7:107221074-107221124	HNPCEpiC	eye:	n/a
12	chr7:107220368-107220418	PFSK-1	brain:	n/a
13	chr7:107221136-107221186	BJ	skin:	n/a
14	chr7:107220262-107220312	PFSK-1	brain:	n/a
15	chr7:107220588-107220638	HUVEC	blood vessel:	n/a
16	chr7:107220368-107220418	HIPEpiC	eye:	n/a
17	chr7:107220080-107220130	SK-N-MC	brain:	n/a
18	chr7:107221327-107221377	NB4	blood:	n/a
19	chr7:107221141-107221191	HCT-116	colon:	n/a
20	chr7:107220040-107220090	NH-A	brain:	n/a
21	chr7:107223076-107223126	HRCEpiC	kidney:	n/a
22	chr7:107220968-107221018	RPTEC	kidney:	n/a
23	chr7:107220262-107220312	HMEC	breast:	n/a
24	chr7:107221141-107221191	GM06990	blood:	n/a
25	chr7:107223076-107223126	HEK293	kidney:	embryo
26	chr7:107220583-107220633	AG09309	skin:	n/a
27	chr7:107220080-107220130	RPTEC	kidney:	n/a
28	chr7:107219178-107219228	GM12892	blood:	n/a
29	chr7:107221327-107221377	HCPEpiC	choroid plexus:	n/a
30	chr7:107220345-107220395	NHDF-neo	bronchial:	n/a
31	chr7:107221136-107221186	CMK	blood:	n/a
32	chr7:107221136-107221186	HRE	kidney:	n/a
33	chr7:107220372-107220422	HRCEpiC	kidney:	n/a
34	chr7:107221327-107221377	HNPCEpiC	eye:	n/a
35	chr7:107220040-107220090	HUVEC	blood vessel:	n/a
36	chr7:107221074-107221124	K562	blood:	n/a
37	chr7:107220080-107220130	HPAEpiC	pulmonary alveolar:	n/a
38	chr7:107220262-107220312	NHDF-neo	bronchial:	n/a
39	chr7:107220040-107220090	HRE	kidney:	n/a
40	chr7:107220968-107221018	CMK	blood:	n/a
41	chr7:107220588-107220638	Hela-S3	cervix:	n/a
42	chr7:107218933-107218983	HAEpiC	amniotic membrane:	n/a
43	chr7:107221327-107221377	MCF-7	breast:	n/a
44	chr7:107221074-107221124	HepG2	liver:	n/a
45	chr7:107220345-107220395	LNCaP	prostate:	n/a
46	chr7:107220040-107220090	PrEC	prostate:	n/a
47	chr7:107220968-107221018	U87	brain:	n/a
48	chr7:107220968-107221018	H1-hESC	embryonic stem cell:	embryo
49	chr7:107221327-107221377	AoSMC	blood vessel:	n/a
50	chr7:107220968-107221018	HRCEpiC	kidney:	n/a

(count:33 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:107209715..107211538-chr7:107214457..107216684,2	MCF-7	breast:
2	chr2:95830717..95831431-chr7:107220273..107221008,2	HCT-116	colon:
3	chr7:107202021..107207492-chr7:107217594..107222531,11	MCF-7	breast:
4	chr7:107214115..107215685-chr7:107530990..107532752,2	K562	blood:
5	chr7:107210647..107213147-chr7:107219031..107221159,5	MCF-7	breast:
6	chr15:67546176..67547027-chr7:107220695..107221206,2	Hela-S3	cervix:
7	chr7:107207110..107210037-chr7:107211935..107213568,2	MCF-7	breast:
8	chr7:106861292..106863138-chr7:107221411..107223026,2	MCF-7	breast:
9	chr7:107210479..107213238-chr7:107221392..107223679,2	MCF-7	breast:
10	chr7:107217896..107220327-chr7:107230749..107233024,2	MCF-7	breast:
11	chr7:107219444..107222929-chr7:107242777..107244829,3	MCF-7	breast:
12	chr7:107219336..107222149-chr7:107234347..107238081,3	MCF-7	breast:
13	chr7:107220536..107223126-chr7:107229561..107233468,4	MCF-7	breast:
14	chr7:107222229..107223878-chr7:107235246..107236796,2	MCF-7	breast:
15	chr7:107213784..107216037-chr7:107241685..107244437,2	K562	blood:
16	chr7:107215856..107218620-chr7:107219373..107220933,2	MCF-7	breast:
17	chr11:62608095..62610646-chr7:107220140..107222919,2	K562	blood:
18	chr7:107209715..107211538-chr7:107214457..107216684,2	MCF-7	breast:
19	chr7:107202798..107206022-chr7:107208738..107213225,6	MCF-7	breast:
20	chr7:107227083..107228609-chr7:107243065..107245394,2	K562	blood:
21	chr12:124196655..124197422-chr7:107220206..107220978,2	Hela-S3	cervix:
22	chr7:107213853..107217373-chr7:107218524..107221215,3	MCF-7	breast:
23	chr7:107190837..107193195-chr7:107215687..107218303,2	K562	blood:
24	chr7:107202748..107209925-chr7:107217558..107222659,11	MCF-7	breast:
25	chr7:107220726..107224521-chr7:107383760..107385958,4	K562	blood:
26	chr7:107188089..107190681-chr7:107220054..107222160,2	MCF-7	breast:
27	chr7:107213853..107217373-chr7:107218524..107221215,3	MCF-7	breast:
28	chr7:107222080..107224411-chr7:107383065..107385260,2	K562	blood:
29	chr1:92763878..92764562-chr7:107220034..107220754,2	Hela-S3	cervix:
30	chr7:107228897..107231407-chr7:107235994..107238690,2	MCF-7	breast:
31	chr7:107221736..107223246-chr7:107253261..107254862,2	K562	blood:
32	chr7:107218928..107223365-chr7:107225949..107230360,6	MCF-7	breast:
33	chr20:25371188..25372153-chr7:107220709..107221225,2	NB4	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-COG5-4	chr7:107220002-107220502	ENSG00000272854.1

No data

Variant related genes	Relation type
BCAP29	TF binding region
ENSG00000272854	TF binding region
DUS4L	TF binding region
BCAP29	CpG island
ENSG00000272854	CpG island
DUS4L	CpG island
ENSG00000103591	chromatin interactions
ENSG00000122484	chromatin interactions
ENSG00000144026	chromatin interactions
ENSG00000133316	chromatin interactions
ENSG00000185344	chromatin interactions
ENSG00000100997	chromatin interactions
ENSG00000164597	chromatin interactions
ENSG00000091140	chromatin interactions
ENSG00000163067	chromatin interactions
ENSG00000272854	chromatin interactions
ENSG00000105865	chromatin interactions
ENSG00000105879	chromatin interactions
ENSG00000174842	chromatin interactions
ENSG00000075790	chromatin interactions
ENSG00000241764	chromatin interactions
ENSG00000238832	chromatin interactions

Extended variants
information (count: 699 )
Associated
traits (count: 81 )

Variant overlapped rSNPs/rCNVs (count:699 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11977187	chr7:107210383-107210384	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs551952050	chr7:107210396-107210397	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs144605001	chr7:107210449-107210450	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs184763463	chr7:107210482-107210483	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs73724536	chr7:107210507-107210508	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs200902355	chr7:107210517-107210518	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs566733616	chr7:107210660-107210661	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
8	rs146686117	chr7:107210679-107210680	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
9	rs34611940	chr7:107210696-107210697	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
10	rs73724537	chr7:107210721-107210722	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs568999649	chr7:107210787-107210788	Weak transcription Strong transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
12	rs570799424	chr7:107210789-107210790	Weak transcription Strong transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
13	rs189222412	chr7:107210791-107210792	Weak transcription Strong transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
14	rs181565997	chr7:107210804-107210805	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
15	rs577326232	chr7:107210816-107210817	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
16	rs186820296	chr7:107210820-107210821	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
17	rs73419470	chr7:107210852-107210853	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs148860103	chr7:107210863-107210864	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
19	rs35598969	chr7:107210906-107210907	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
20	rs35495251	chr7:107210927-107210928	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
21	rs191356156	chr7:107210930-107210931	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
22	rs143753503	chr7:107210938-107210939	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
23	rs576515118	chr7:107210959-107210960	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
24	rs574897518	chr7:107210997-107210998	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
25	rs545627783	chr7:107211083-107211084	Weak transcription Strong transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
26	rs148153218	chr7:107211125-107211126	Weak transcription Strong transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
27	rs386716615	chr7:107211169-107211170	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
28	rs75194040	chr7:107211170-107211171	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
29	rs181370516	chr7:107211185-107211186	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
30	rs541924342	chr7:107211199-107211200	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
31	rs529181849	chr7:107211298-107211299	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
32	rs60691712	chr7:107211326-107211327	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs569133917	chr7:107211337-107211338	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
34	rs373241660	chr7:107211344-107211345	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
35	rs146893470	chr7:107211412-107211413	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
36	rs551176616	chr7:107211423-107211424	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
37	rs139353007	chr7:107211466-107211467	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
38	rs377539510	chr7:107211550-107211551	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
39	rs533668907	chr7:107211589-107211590	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
40	rs117079685	chr7:107211632-107211633	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
41	rs145775949	chr7:107211638-107211639	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
42	rs141539487	chr7:107211657-107211658	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
43	rs371069795	chr7:107211693-107211694	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
44	rs201110775	chr7:107211703-107211704	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
45	rs368237773	chr7:107211713-107211714	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
46	rs200673623	chr7:107211727-107211728	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
47	rs376756210	chr7:107211732-107211733	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
48	rs376839581	chr7:107211893-107211894	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
49	rs186056160	chr7:107211922-107211923	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
50	rs572225058	chr7:107211936-107211937	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:81)

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
T-cell prolymphocytic leukemia	19278963	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
Acute lymphoblastic leukemia	22237106	CNVD
Breast cancer	21364760	CNVD
lymphocytic leukemia	21291569	CNVD
Basal cell lymphoma	17053054	CNVD
Prostate cancer	16573809	CNVD
Medulloblastoma	16783165	CNVD
Melanoma	17363583	CNVD
Pancreatic cancer	17952125	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Myelofibrosis	22110671	CNVD
Squamous cell cancer	20885788	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Breast cancer	16397240	CNVD
Biliary cancer	19435499	CNVD
Non-small cell lung cancer	21829676	CNVD
Ovarian neoplasms	16753589	CNVD
Prostate cancer	23792589	CNVD
Adenocarcinoma	21044232	CNVD
Splenic marginal zone lymphoma	21957467	CNVD

Chromatin state (count:1004 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:107204800-107210600	Weak transcription	Spleen	Spleen
2	chr7:107205000-107210600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
3	chr7:107205000-107219600	Weak transcription	Pancreas	Pancrea
4	chr7:107205000-107220000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
5	chr7:107205000-107220000	Weak transcription	Gastric	stomach
6	chr7:107205000-107220200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
7	chr7:107205000-107220200	Weak transcription	Sigmoid Colon	Sigmoid Colon
8	chr7:107205200-107210400	Weak transcription	Fetal Thymus	thymus
9	chr7:107205200-107210600	Weak transcription	Primary T cells fromperipheralblood	blood
10	chr7:107205200-107210600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
11	chr7:107205200-107210600	Weak transcription	Fetal Muscle Trunk	muscle
12	chr7:107205200-107210600	Weak transcription	Fetal Muscle Leg	muscle
13	chr7:107205200-107210600	Weak transcription	Placenta	Placenta
14	chr7:107205200-107210600	Weak transcription	Left Ventricle	heart
15	chr7:107205200-107210800	Weak transcription	Ovary	ovary
16	chr7:107205200-107219600	Weak transcription	Esophagus	oesophagus
17	chr7:107205200-107219600	Weak transcription	Right Ventricle	heart
18	chr7:107205200-107220000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
19	chr7:107205200-107220000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
20	chr7:107205200-107220000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
21	chr7:107205200-107220000	Weak transcription	Lung	lung
22	chr7:107205200-107220000	Weak transcription	Psoas Muscle	Psoas
23	chr7:107205400-107210600	Weak transcription	Primary monocytes fromperipheralblood	blood
24	chr7:107205400-107210800	Weak transcription	Primary B cells from peripheral blood	blood
25	chr7:107205400-107211800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
26	chr7:107205400-107219800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
27	chr7:107205400-107220000	Weak transcription	Primary neutrophils fromperipheralblood	blood
28	chr7:107205400-107220000	Weak transcription	Colonic Mucosa	Colon
29	chr7:107205400-107220000	Weak transcription	Placenta Amnion	Placenta Amnion
30	chr7:107205600-107210400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
31	chr7:107205600-107210400	Weak transcription	Monocytes-CD14+_RO01746	blood
32	chr7:107205600-107210600	Weak transcription	Duodenum Mucosa	Duodenum
33	chr7:107205600-107210600	Weak transcription	Fetal Brain Female	brain
34	chr7:107205600-107210800	Weak transcription	Adipose Nuclei	Adipose
35	chr7:107205600-107210800	Weak transcription	Liver	Liver
36	chr7:107205600-107210800	Weak transcription	Fetal Intestine Large	intestine
37	chr7:107205600-107211600	Weak transcription	H1 Cell Line	embryonic stem cell
38	chr7:107205600-107211600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
39	chr7:107205600-107211800	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
40	chr7:107205600-107211800	Weak transcription	Stomach Smooth Muscle	stomach
41	chr7:107205600-107214000	Weak transcription	Small Intestine	intestine
42	chr7:107205600-107215200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
43	chr7:107205600-107215400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
44	chr7:107205600-107215400	Weak transcription	Rectal Mucosa Donor 31	rectum
45	chr7:107205600-107219600	Weak transcription	Aorta	Aorta
46	chr7:107205600-107219600	Weak transcription	Fetal Stomach	stomach
47	chr7:107205600-107219600	Weak transcription	Rectal Smooth Muscle	rectum
48	chr7:107205600-107219800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
49	chr7:107205600-107220000	Weak transcription	H9 Cell Line	embryonic stem cell
50	chr7:107205600-107220000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived

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