Variant report

Variant	nsv539472
Chromosome Location	chr8:10618928-10652924
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:592)
CpG islands
(count:794)
Chromatin interactive
region (count:29)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:592 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:10618425-10619055	K562	blood:	n/a	n/a
2	ARID3A	chr8:10629194-10629470	K562	blood:	n/a	n/a
3	ARID3A	chr8:10631175-10631647	K562	blood:	n/a	n/a
4	ARID3A	chr8:10638845-10638952	K562	blood:	n/a	n/a
5	ARID3A	chr8:10634540-10635222	K562	blood:	n/a	n/a
6	ARID3A	chr8:10632964-10633416	K562	blood:	n/a	n/a
7	ATF1	chr8:10629162-10629538	K562	blood:	n/a	n/a
8	ATF1	chr8:10634783-10635469	K562	blood:	n/a	n/a
9	ATF2	chr8:10646076-10646653	GM12878	blood:	n/a	n/a
10	ATF2	chr8:10641139-10641593	GM12878	blood:	n/a	n/a
11	ATF2	chr8:10641097-10641653	GM12878	blood:	n/a	n/a
12	ATF2	chr8:10646115-10646583	GM12878	blood:	n/a	n/a
13	ATF3	chr8:10634812-10635209	K562	blood:	n/a	n/a
14	BACH1	chr8:10634535-10634552	K562	blood:	n/a	n/a
15	BATF	chr8:10641195-10641508	GM12878	blood:	n/a	chr8:10641369-10641380
16	BATF	chr8:10646148-10646551	GM12878	blood:	n/a	chr8:10646312-10646323
17	BATF	chr8:10641154-10641577	GM12878	blood:	n/a	chr8:10641369-10641380
18	BCL11A	chr8:10646180-10646518	GM12878	blood:	n/a	n/a
19	BCL11A	chr8:10641274-10641544	GM12878	blood:	n/a	n/a
20	BCL3	chr8:10646199-10646599	GM12878	blood:	n/a	n/a
21	BHLHE40	chr8:10629130-10629563	K562	blood:	n/a	n/a
22	BHLHE40	chr8:10633148-10633444	K562	blood:	n/a	n/a
23	BHLHE40	chr8:10618383-10618969	K562	blood:	n/a	n/a
24	BHLHE40	chr8:10646418-10646431	K562	blood:	n/a	n/a
25	BHLHE40	chr8:10648112-10648199	K562	blood:	n/a	n/a
26	BHLHE40	chr8:10634083-10635624	K562	blood:	n/a	n/a
27	BRCA1	chr8:10645582-10645644	Hela-S3	cervix:	n/a	n/a
28	BRCA1	chr8:10647677-10647797	H1-hESC	embryonic stem cell:	n/a	n/a
29	CBX3	chr8:10634548-10635220	K562	blood:	n/a	n/a
30	CBX3	chr8:10634712-10635188	K562	blood:	n/a	n/a
31	CCNT2	chr8:10633114-10633530	K562	blood:	n/a	n/a
32	CCNT2	chr8:10634549-10635416	K562	blood:	n/a	chr8:10634941-10634961
33	CEBPB	chr8:10633143-10633386	K562	blood:	n/a	n/a
34	CEBPB	chr8:10634441-10635158	K562	blood:	n/a	n/a
35	CEBPB	chr8:10634708-10635140	K562	blood:	n/a	n/a
36	CEBPB	chr8:10646189-10646640	IMR90	lung:	n/a	n/a
37	CEBPB	chr8:10646288-10646647	H1-hESC	embryonic stem cell:	n/a	n/a
38	CEBPB	chr8:10646341-10646362	HepG2	liver:	n/a	n/a
39	CEBPB	chr8:10646913-10647240	IMR90	lung:	n/a	n/a
40	CEBPB	chr8:10651229-10651497	MCF-7	breast:	n/a	n/a
41	CEBPB	chr8:10651152-10651628	Hela-S3	cervix:	n/a	n/a
42	CEBPB	chr8:10646017-10646745	GM12878	blood:	n/a	n/a
43	CEBPB	chr8:10633137-10633489	K562	blood:	n/a	n/a
44	CEBPB	chr8:10618410-10618990	K562	blood:	n/a	n/a
45	CEBPB	chr8:10628458-10628576	HepG2	liver:	n/a	n/a
46	CEBPB	chr8:10624393-10624563	K562	blood:	n/a	chr8:10624528-10624541
47	CEBPD	chr8:10634708-10635711	K562	blood:	n/a	n/a
48	CEBPD	chr8:10634773-10635305	K562	blood:	n/a	n/a
49	CHD2	chr8:10646434-10646564	H1-hESC	embryonic stem cell:	n/a	n/a
50	CHD2	chr8:10634134-10635160	K562	blood:	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	chr8:10643634-10643684	NH-A	brain:	n/a
2	chr8:10643634-10643684	NH-A	brain:	n/a
3	chr8:10621801-10621851	HPAEpiC	pulmonary alveolar:	n/a
4	chr8:10622805-10622855	ECC-1	luminal epithelium:	n/a
5	chr8:10622887-10622937	K562	blood:	n/a
6	chr8:10621874-10621924	A549	lung:	n/a
7	chr8:10623534-10623584	AG04450	lung:	fetal
8	chr8:10650046-10650096	GM19239	blood:	n/a
9	chr8:10621935-10621985	AG04449	skin:	fetal
10	chr8:10650046-10650096	SAEC	small airway:	n/a
11	chr8:10622887-10622937	Caco-2	colon:	n/a
12	chr8:10635419-10635469	U87	brain:	n/a
13	chr8:10622887-10622937	AG04449	skin:	fetal
14	chr8:10623038-10623088	PrEC	prostate:	n/a
15	chr8:10650046-10650096	AG04449	skin:	fetal
16	chr8:10621801-10621851	ECC-1	luminal epithelium:	n/a
17	chr8:10635419-10635469	Jurkat	blood:	n/a
18	chr8:10622887-10622937	SK-N-SH	brain:	n/a
19	chr8:10650046-10650096	NHDF-neo	bronchial:	n/a
20	chr8:10621935-10621985	AG09309	skin:	n/a
21	chr8:10623534-10623584	SKMC	muscle:	n/a
22	chr8:10646690-10646740	BE2_C	brain:	n/a
23	chr8:10622805-10622855	A549	lung:	n/a
24	chr8:10623344-10623394	AG04450	lung:	fetal
25	chr8:10621874-10621924	BJ	skin:	n/a
26	chr8:10623534-10623584	PFSK-1	brain:	n/a
27	chr8:10623038-10623088	AG04450	lung:	fetal
28	chr8:10643634-10643684	HepG2	liver:	n/a
29	chr8:10622805-10622855	Jurkat	blood:	n/a
30	chr8:10623038-10623088	HNPCEpiC	eye:	n/a
31	chr8:10623534-10623584	A549	lung:	n/a
32	chr8:10635419-10635469	PrEC	prostate:	n/a
33	chr8:10622887-10622937	MCF-7	breast:	n/a
34	chr8:10650046-10650096	HEK293	kidney:	embryo
35	chr8:10621874-10621924	AG10803	skin:	n/a
36	chr8:10623038-10623088	AG04449	skin:	fetal
37	chr8:10622887-10622937	GM12892	blood:	n/a
38	chr8:10635419-10635469	GM06990	blood:	n/a
39	chr8:10650046-10650096	HRCEpiC	kidney:	n/a
40	chr8:10643634-10643684	HL-60	blood:	n/a
41	chr8:10623344-10623394	GM12891	blood:	n/a
42	chr8:10623534-10623584	HCT-116	colon:	n/a
43	chr8:10622805-10622855	HRPEpiC	eye:	n/a
44	chr8:10621874-10621924	GM19239	blood:	n/a
45	chr8:10621874-10621924	HUVEC	blood vessel:	n/a
46	chr8:10621801-10621851	PANC-1	pancreas:	n/a
47	chr8:10621801-10621851	NB4	blood:	n/a
48	chr8:10650046-10650096	IMR90	lung:	fetal
49	chr8:10622887-10622937	SK-N-SH_RA	brain:	n/a
50	chr8:10623038-10623088	HCF	heart:	n/a

(count:29 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr8:10620237..10621942-chr8:10624836..10626716,2	K562	blood:
2	chr8:10616130..10621063-chr8:10631004..10634975,5	K562	blood:
3	chr8:10647998..10650941-chr8:10651803..10654879,3	K562	blood:
4	chr8:10634439..10636776-chr8:10637920..10639941,2	K562	blood:
5	chr8:10620237..10621942-chr8:10624836..10626716,2	K562	blood:
6	chr8:10633410..10636281-chr8:10695946..10698229,2	K562	blood:
7	chr8:10648353..10650941-chr8:10651549..10653303,2	K562	blood:
8	chr8:10637227..10639658-chr8:10641198..10643629,3	K562	blood:
9	chr8:10616130..10621063-chr8:10631004..10634975,5	K562	blood:
10	chr8:10621941..10624619-chr8:10627842..10631333,3	K562	blood:
11	chr8:10644063..10645864-chr8:10646300..10647918,2	K562	blood:
12	chr8:10615706..10617702-chr8:10620374..10622044,2	K562	blood:
13	chr8:10611693..10613429-chr8:10616715..10619425,2	K562	blood:
14	chr8:10515210..10517092-chr8:10648053..10650432,2	K562	blood:
15	chr8:10628530..10631997-chr8:10633640..10636320,4	K562	blood:
16	chr8:10621941..10624619-chr8:10627842..10631333,3	K562	blood:
17	chr8:10628530..10631997-chr8:10633640..10636320,4	K562	blood:
18	chr8:10648269..10650512-chr8:10653379..10655643,2	K562	blood:
19	chr8:10647998..10650941-chr8:10651803..10654879,3	K562	blood:
20	chr8:10644063..10645864-chr8:10646300..10647918,2	K562	blood:
21	chr8:10622933..10625831-chr8:10627358..10629898,3	K562	blood:
22	chr8:10631743..10634256-chr8:10658449..10660185,2	K562	blood:
23	chr8:10640744..10643813-chr8:10646247..10648006,3	K562	blood:
24	chr8:10622933..10625831-chr8:10627358..10629898,3	K562	blood:
25	chr8:10635373..10637028-chr8:10639267..10640869,2	MCF-7	breast:
26	chr8:10634439..10636776-chr8:10637920..10639941,2	K562	blood:
27	chr8:10651485..10654382-chr8:10658663..10661335,2	K562	blood:
28	chr8:10635373..10637028-chr8:10639267..10640869,2	MCF-7	breast:
29	chr8:10648353..10650941-chr8:10651549..10653303,2	K562	blood:

(count:6 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C8orf74-1	chr8:10622680-10622686	NONHSAT125014
2	lnc-C8orf74-1	chr8:10621847-10622233	ENSG00000248896
3	lnc-C8orf74-4	chr8:10649122-10649238	ucscGeneNc_uc003wtg_1
4	lnc-C8orf74-1	chr8:10628705-10628902	ENSG00000248896
5	lnc-C8orf74-4	chr8:10624234-10624550	ucscGeneNc_uc003wtg_1
6	lnc-C8orf74-1	chr8:10621847-10622667	NONHSAT125014

No data

Variant related genes	Relation type
ENSG00000252565	TF binding region
ENSG00000252565	CpG island
ENSG00000253695	chromatin interactions
ENSG00000258724	chromatin interactions
ENSG00000252565	chromatin interactions
ENSG00000254093	chromatin interactions
HSPA1B	miRNA target sites

Extended variants
information (count: 1930 )
Associated
traits (count: 148 )

Variant overlapped rSNPs/rCNVs (count:1930 , 50 per page) page: 1 2 3 4 5 6 7 ... 39

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs567197027	chr8:10618934-10618935	Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
2	rs555775277	chr8:10618935-10618936	Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
3	rs74627156	chr8:10618936-10618937	Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
4	rs575840304	chr8:10618953-10618954	Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
5	rs566342139	chr8:10618954-10618955	Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
6	rs544708012	chr8:10618969-10618970	Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
7	rs535315262	chr8:10618983-10618984	Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
8	rs116689595	chr8:10619029-10619030	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs554606640	chr8:10619039-10619040	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs73662619	chr8:10619050-10619051	Weak transcription Enhancers Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs373256900	chr8:10619120-10619121	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs557382265	chr8:10619122-10619123	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs187645715	chr8:10619138-10619139	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs564715622	chr8:10619145-10619146	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs17152293	chr8:10619165-10619166	Weak transcription Enhancers Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs533364059	chr8:10619192-10619193	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs540780039	chr8:10619193-10619194	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs17152296	chr8:10619230-10619231	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs572828181	chr8:10619256-10619257	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs188224342	chr8:10619267-10619268	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs11250069	chr8:10619272-10619273	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs145137369	chr8:10619296-10619297	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs564345373	chr8:10619308-10619309	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs550406341	chr8:10619332-10619333	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs372514069	chr8:10619346-10619347	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs111577490	chr8:10619350-10619351	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs370047197	chr8:10619382-10619383	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs184200157	chr8:10619385-10619386	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs566460909	chr8:10619460-10619461	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs149455334	chr8:10619509-10619510	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs34436305	chr8:10619544-10619545	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs552100991	chr8:10619593-10619594	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs571873810	chr8:10619618-10619619	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs188342101	chr8:10619621-10619622	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs557192256	chr8:10619628-10619629	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs4392861	chr8:10619649-10619650	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs548738918	chr8:10619737-10619738	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs574054130	chr8:10619757-10619758	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs180745520	chr8:10619776-10619777	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs184665367	chr8:10619778-10619779	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs189513742	chr8:10619785-10619786	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs143895261	chr8:10619834-10619835	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs114728478	chr8:10619844-10619845	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs575358269	chr8:10619859-10619860	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs544359919	chr8:10619873-10619874	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs78108706	chr8:10619874-10619875	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs148214815	chr8:10619901-10619902	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs114347407	chr8:10619908-10619909	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs372722352	chr8:10619910-10619911	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs17152300	chr8:10619919-10619920	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:148)

Disease	PMID	Source
Crohn''s disease	19220326	CNVD
Psoriasis	19220326	CNVD
Prostate cancer	21965145	CNVD
Prostate cancer	18515986	CNVD
Chronic obstructive pulmonary disease	20378733	CNVD
Autism	18414403	CNVD
Cancer	21183584	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Breast cancer	17603634	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Ovarian cancer	20844748	CNVD
Cervical cancer	17311676	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Schizophrenia	20877625	CNVD
Disorders of sex development	21048976	CNVD
Colorectal cancer	16272173	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Breast cancer	17001317	CNVD
Thyroid cancer	19087340	CNVD
Multiple myeloma	16616336	CNVD
Hepatocellular carcinoma	22174799	CNVD
Heart disease	21282601	CNVD
Prostate cancer	16573809	CNVD
T-cell lymphomas	19863542	CNVD
Ovarian cancer	22174824	CNVD
Colorectal cancer	21297112	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Salivary gland tumor	18059337	CNVD
Breast cancer	17133270	CNVD
Melanoma	18172304	CNVD
Medulloblastoma	21979893	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Breast cancer	17393978	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Cancer	21637783	CNVD
Breast cancer	20837533	CNVD
Squamous cell cancer	21044232	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	22429812	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Colorectal cancer	20709793	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Basal cell lymphoma	21115979	CNVD
Breast cancer	21264507	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Oral cancer	21386901	CNVD
Prostate cancer	21088497	CNVD
Breast cancer	20940404	CNVD
Colorectal cancer	19359472	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Gastric cancer	17167181	CNVD
Prostate cancer	16705090	CNVD
8p-syndrome	17576883	CNVD
Human rectal carcinomas	16397240	CNVD
Medulloblastoma	16968546	CNVD
Lung adenocarcinoma	19525976	CNVD
Lung cancer	19525976	CNVD
Prostate cancer	17245344	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Cancer	16751803	CNVD
Wilms tumour	21544195	CNVD
Gastric cancer	17908304	CNVD
Autism	19415332	CNVD
Malaria	21533027	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Esophageal cancer	21851588	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Breast cancer	21245420	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Breast cancer	21785460	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Acute myeloid leukemia	20729466	CNVD
Breast cancer	21509527	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Acute myeloid leukemia	21251322	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21858162	CNVD
lymphocytic leukemia	21291569	CNVD
Liver carcinoma	19366792	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Congenital diaphragmatic hernia	21064195	CNVD
Autism	22495311	CNVD
Myelofibrosis	22110671	CNVD
Intellectual disability	22045946	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	16608533	CNVD
Seminomas	18059402	CNVD
Lung cancer	18438408	CNVD
Lung squamous cell carcinoma	22363434	CNVD
Medulloblastoma	16783165	CNVD
Gastric cancer	18160780	CNVD
Breast cancer	21990379	CNVD
Psoriasis	20403174	CNVD
Psoriasis	20663923	CNVD
Crohn''s disease	16909382	CNVD
Cancer	21129771	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Crohn''s disease	20877625	CNVD
Inflammatory disorder	20877625	CNVD
Cardiac defect	21933911	CNVD
Psoriasis	18059266	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Psoriasis	20877625	CNVD
Mental retardation	17847001	CNVD
Prostate cancer	17217626	CNVD
Schizophrenia	21399695	CNVD
Colorectal cancer	21128281	CNVD
Colorectal cancer	19455253	CNVD
Psoriasis	18848619	CNVD
Squamous cell cancer	19047905	CNVD
Colorectal cancer	17229543	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Myxofibrosarcoma	16751306	CNVD
Immune disease	21572526	CNVD
Non-small cell lung cancer	21829676	CNVD
Ovarian neoplasms	16753589	CNVD
Kallmann Syndrome 2	22470819	CNVD
Developmental disorder	20461109	CNVD
abnormal development	18461090	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Glioblastoma multiforme	21138945	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21364760	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Gastric cancer	21811585	CNVD
Colorectal cancer	16774939	CNVD
Lung adenocarcinoma	21935476	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Renal cell carcinoma	21215367	CNVD
Osteosarcoma	21215367	CNVD
Schizophrenia	23813976	CNVD

Chromatin state (count:1034 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:10610000-10621400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
2	chr8:10610600-10620400	Weak transcription	HepG2	liver
3	chr8:10610800-10622200	Weak transcription	Primary B cells from cord blood	blood
4	chr8:10610800-10662000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
5	chr8:10611200-10624400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
6	chr8:10612600-10621600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
7	chr8:10612800-10621600	Weak transcription	Spleen	Spleen
8	chr8:10613200-10622600	Weak transcription	Duodenum Smooth Muscle	Duodenum
9	chr8:10613400-10621600	Weak transcription	Aorta	Aorta
10	chr8:10614200-10621400	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
11	chr8:10614400-10634200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
12	chr8:10614800-10621400	Weak transcription	Left Ventricle	heart
13	chr8:10614800-10621400	Weak transcription	Lung	lung
14	chr8:10614800-10621800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
15	chr8:10614800-10622000	Weak transcription	Hela-S3	cervix
16	chr8:10615000-10621400	Weak transcription	Adipose Nuclei	Adipose
17	chr8:10615400-10620800	Weak transcription	Primary T helper cells fromperipheralblood	blood
18	chr8:10615400-10621400	Weak transcription	HUES64 Cell Line	embryonic stem cell
19	chr8:10615600-10621600	Weak transcription	Dnd41	blood
20	chr8:10615800-10621400	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
21	chr8:10615800-10621600	Weak transcription	Gastric	stomach
22	chr8:10616600-10621600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
23	chr8:10616800-10621200	Weak transcription	H9 Cell Line	embryonic stem cell
24	chr8:10617200-10620800	Weak transcription	Primary T helper cells PMA-I stimulated	--
25	chr8:10617200-10621200	Weak transcription	Stomach Smooth Muscle	stomach
26	chr8:10617400-10621600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
27	chr8:10617600-10619200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
28	chr8:10617600-10619200	Enhancers	NHEK	skin
29	chr8:10617600-10621400	Weak transcription	Primary T cells fromperipheralblood	blood
30	chr8:10617800-10619000	Enhancers	Duodenum Mucosa	Duodenum
31	chr8:10617800-10619200	Active TSS	Brain Substantia Nigra	brain
32	chr8:10617800-10620000	Weak transcription	Primary T cells from cord blood	blood
33	chr8:10618000-10621400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
34	chr8:10618000-10621600	Weak transcription	Esophagus	oesophagus
35	chr8:10618000-10622000	Weak transcription	Fetal Thymus	thymus
36	chr8:10618000-10634400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
37	chr8:10618200-10619000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
38	chr8:10618200-10619000	Enhancers	Placenta Amnion	Placenta Amnion
39	chr8:10618200-10621400	Weak transcription	Thymus	Thymus
40	chr8:10618400-10619000	Flanking Active TSS	Brain Hippocampus Middle	brain
41	chr8:10618400-10619000	Bivalent Enhancer	Fetal Heart	heart
42	chr8:10618400-10619200	Enhancers	Placenta	Placenta
43	chr8:10618400-10619200	Enhancers	Stomach Mucosa	stomach
44	chr8:10618400-10621200	Weak transcription	A549	lung
45	chr8:10618600-10619000	Flanking Active TSS	K562	blood
46	chr8:10618600-10619200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
47	chr8:10618600-10619200	Enhancers	Fetal Muscle Trunk	muscle
48	chr8:10618600-10619200	Enhancers	Ovary	ovary
49	chr8:10618600-10621000	Weak transcription	HMEC	breast
50	chr8:10618600-10621600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived

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