Variant report

Variant	nsv885795
Chromosome Location	chr6:34704613-34823187
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2298)
CpG islands
(count:1712)
Chromatin interactive
region (count:159)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:3)

(count:2298 , 50 per page) page: 1 2 3 4 5 6 7 ... 46

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:34724272-34725451	HepG2	liver:	n/a	n/a
2	ARID3A	chr6:34759163-34759895	HepG2	liver:	n/a	n/a
3	ARID3A	chr6:34744211-34744366	K562	blood:	n/a	n/a
4	ARID3A	chr6:34759766-34759905	K562	blood:	n/a	n/a
5	ARID3A	chr6:34763588-34764041	HepG2	liver:	n/a	n/a
6	ARID3A	chr6:34778815-34779244	HepG2	liver:	n/a	n/a
7	ARID3A	chr6:34760664-34761063	HepG2	liver:	n/a	n/a
8	ARID3A	chr6:34724840-34725300	K562	blood:	n/a	n/a
9	ARID3A	chr6:34709883-34710222	HepG2	liver:	n/a	n/a
10	ARID3A	chr6:34707133-34707243	HepG2	liver:	n/a	n/a
11	ARID3A	chr6:34708045-34708073	K562	blood:	n/a	n/a
12	ARID3A	chr6:34802936-34803203	K562	blood:	n/a	n/a
13	ARID3A	chr6:34807829-34807953	K562	blood:	n/a	n/a
14	ARID3A	chr6:34713147-34714396	HepG2	liver:	n/a	n/a
15	ARID3A	chr6:34712925-34713484	K562	blood:	n/a	n/a
16	ARID3A	chr6:34724265-34724568	K562	blood:	n/a	n/a
17	ARID3A	chr6:34708281-34708419	HepG2	liver:	n/a	n/a
18	ATF1	chr6:34803008-34803279	K562	blood:	n/a	n/a
19	ATF1	chr6:34724842-34725509	K562	blood:	n/a	n/a
20	ATF1	chr6:34784452-34784735	K562	blood:	n/a	n/a
21	ATF1	chr6:34744205-34744329	K562	blood:	n/a	n/a
22	ATF1	chr6:34712995-34713537	K562	blood:	n/a	n/a
23	ATF2	chr6:34778788-34779343	GM12878	blood:	n/a	n/a
24	ATF2	chr6:34724744-34725530	H1-hESC	embryonic stem cell:	n/a	n/a
25	ATF2	chr6:34778634-34779486	GM12878	blood:	n/a	n/a
26	ATF2	chr6:34725075-34725581	H1-hESC	embryonic stem cell:	n/a	n/a
27	ATF2	chr6:34724776-34725771	GM12878	blood:	n/a	n/a
28	ATF2	chr6:34724812-34725445	GM12878	blood:	n/a	n/a
29	ATF3	chr6:34760499-34760914	H1-hESC	embryonic stem cell:	n/a	n/a
30	ATF3	chr6:34724532-34725607	HepG2	liver:	n/a	chr6:34725266-34725286
31	ATF3	chr6:34724990-34725522	A549	lung:	n/a	chr6:34725266-34725286
32	ATF3	chr6:34725040-34725451	HepG2	liver:	n/a	chr6:34725266-34725286
33	ATF3	chr6:34725064-34725443	H1-hESC	embryonic stem cell:	n/a	chr6:34725266-34725286
34	ATF3	chr6:34724989-34725509	H1-hESC	embryonic stem cell:	n/a	chr6:34725266-34725286
35	ATF3	chr6:34725065-34725498	K562	blood:	n/a	chr6:34725266-34725286
36	ATF3	chr6:34724639-34725541	GM12878	blood:	n/a	chr6:34725266-34725286
37	ATF3	chr6:34760514-34760932	K562	blood:	n/a	n/a
38	ATF3	chr6:34713058-34713580	K562	blood:	n/a	n/a
39	ATF3	chr6:34759578-34760020	K562	blood:	n/a	n/a
40	ATF3	chr6:34725126-34725399	GM12878	blood:	n/a	chr6:34725266-34725286
41	ATF3	chr6:34724667-34724975	K562	blood:	n/a	n/a
42	ATF3	chr6:34724772-34725493	K562	blood:	n/a	chr6:34725266-34725286
43	ATF3	chr6:34760493-34760861	H1-hESC	embryonic stem cell:	n/a	n/a
44	BACH1	chr6:34807714-34807998	H1-hESC	embryonic stem cell:	n/a	n/a
45	BACH1	chr6:34760955-34761004	K562	blood:	n/a	n/a
46	BACH1	chr6:34787485-34787796	K562	blood:	n/a	n/a
47	BACH1	chr6:34724717-34724862	K562	blood:	n/a	n/a
48	BACH1	chr6:34807689-34808041	K562	blood:	n/a	n/a
49	BACH1	chr6:34759646-34760379	H1-hESC	embryonic stem cell:	n/a	n/a
50	BATF	chr6:34778725-34779423	GM12878	blood:	n/a	n/a

(count:1712 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:34725144-34725194	NB4	blood:	n/a
2	chr6:34759622-34759672	HEEpiC	esophagus:	n/a
3	chr6:34724756-34724806	T-47D	breast:	n/a
4	chr6:34725359-34725409	AG09309	skin:	n/a
5	chr6:34725144-34725194	NB4	blood:	n/a
6	chr6:34759622-34759672	HEEpiC	esophagus:	n/a
7	chr6:34724756-34724806	T-47D	breast:	n/a
8	chr6:34725359-34725409	AG09309	skin:	n/a
9	chr6:34728146-34728196	HNPCEpiC	eye:	n/a
10	chr6:34722032-34722082	ProgFib	skin:	n/a
11	chr6:34760070-34760120	AG09319	gingival:	n/a
12	chr6:34760070-34760120	HAEpiC	amniotic membrane:	n/a
13	chr6:34724739-34724789	A549	lung:	n/a
14	chr6:34724741-34724791	Caco-2	colon:	n/a
15	chr6:34762855-34762905	RPTEC	kidney:	n/a
16	chr6:34725573-34725623	ECC-1	luminal epithelium:	n/a
17	chr6:34722032-34722082	U87	brain:	n/a
18	chr6:34725116-34725166	U87	brain:	n/a
19	chr6:34759629-34759679	MCF-7	breast:	n/a
20	chr6:34760872-34760922	SKMC	muscle:	n/a
21	chr6:34760070-34760120	ovcar-3	ovarian:	n/a
22	chr6:34759890-34759940	CMK	blood:	n/a
23	chr6:34759018-34759068	Jurkat	blood:	n/a
24	chr6:34759622-34759672	Hela-S3	cervix:	n/a
25	chr6:34760070-34760120	K562	blood:	n/a
26	chr6:34724739-34724789	HCT-116	colon:	n/a
27	chr6:34722032-34722082	HIPEpiC	eye:	n/a
28	chr6:34759549-34759599	ProgFib	skin:	n/a
29	chr6:34725116-34725166	RPTEC	kidney:	n/a
30	chr6:34723499-34723549	HRE	kidney:	n/a
31	chr6:34759890-34759940	HPAEpiC	pulmonary alveolar:	n/a
32	chr6:34725288-34725338	GM19239	blood:	n/a
33	chr6:34722032-34722082	SAEC	small airway:	n/a
34	chr6:34759645-34759695	HRE	kidney:	n/a
35	chr6:34760183-34760233	HCT-116	colon:	n/a
36	chr6:34762855-34762905	MCF-7	breast:	n/a
37	chr6:34724751-34724801	AG04449	skin:	fetal
38	chr6:34728146-34728196	A549	lung:	n/a
39	chr6:34725116-34725166	HAEpiC	amniotic membrane:	n/a
40	chr6:34753792-34753842	HEEpiC	esophagus:	n/a
41	chr6:34725144-34725194	HCT-116	colon:	n/a
42	chr6:34759158-34759208	SK-N-SH	brain:	n/a
43	chr6:34760872-34760922	ovcar-3	ovarian:	n/a
44	chr6:34759629-34759679	NHDF-neo	bronchial:	n/a
45	chr6:34725288-34725338	HIPEpiC	eye:	n/a
46	chr6:34760872-34760922	HEEpiC	esophagus:	n/a
47	chr6:34724751-34724801	RPTEC	kidney:	n/a
48	chr6:34759549-34759599	T-47D	breast:	n/a
49	chr6:34723390-34723440	HRE	kidney:	n/a
50	chr6:34759018-34759068	T-47D	breast:	n/a

(count:159 , 50 per page) page: 1 2 3 4

No.	Distal block	Cell Line	Cell type
1	chr6:34711350..34714841-chr6:34715861..34719730,5	K562	blood:
2	chr6:34723587..34727193-chr6:34757798..34760917,6	K562	blood:
3	chr6:34747403..34749848-chr6:34763943..34765604,2	K562	blood:
4	chr6:34715331..34716988-chr6:34717011..34719994,2	MCF-7	breast:
5	chr6:34786614..34789043-chr6:34809197..34812183,2	K562	blood:
6	chr6:34723785..34726777-chr6:34759451..34763099,4	MCF-7	breast:
7	chr3:42622951..42623830-chr6:34759784..34760772,2	Hela-S3	cervix:
8	chr6:34604156..34606988-chr6:34735347..34736986,2	K562	blood:
9	chr3:87039890..87040592-chr6:34759297..34760271,2	Hela-S3	cervix:
10	chr6:34713112..34714744-chr6:34728866..34731406,2	K562	blood:
11	chr6:34706864..34709056-chr6:34722827..34726268,3	K562	blood:
12	chr6:34663247..34666234-chr6:34723415..34727175,3	K562	blood:
13	chr6:34759093..34761380-chr6:34773456..34776260,3	MCF-7	breast:
14	chr6:34759044..34761297-chr6:34854138..34856970,2	K562	blood:
15	chr6:34723587..34727193-chr6:34757798..34760917,6	K562	blood:
16	chr6:34759998..34762126-chr6:34777640..34780581,3	MCF-7	breast:
17	chr6:34723754..34729214-chr6:34758122..34762652,9	MCF-7	breast:
18	chr6:34773906..34776367-chr6:34780573..34782825,3	MCF-7	breast:
19	chr6:34782930..34784591-chr6:34786044..34787965,3	K562	blood:
20	chr6:34822875..34823681-chr6:34855389..34856282,2	MCF-7	breast:
21	chr6:34766487..34768017-chr6:34768544..34771127,2	MCF-7	breast:
22	chr6:34203757..34206607-chr6:34730565..34733013,2	K562	blood:
23	chr6:34759673..34761787-chr6:34787706..34790146,2	MCF-7	breast:
24	chr6:34726193..34732287-chr6:34732320..34736678,10	K562	blood:
25	chr6:34759673..34761787-chr6:34787706..34790146,2	MCF-7	breast:
26	chr6:34735510..34738429-chr6:34758057..34759743,2	MCF-7	breast:
27	chr6:34727618..34732287-chr6:34732833..34737608,8	K562	blood:
28	chr6:34723520..34726444-chr6:34854512..34857469,3	MCF-7	breast:
29	chr6:34759495..34761419-chr6:34776701..34778831,2	K562	blood:
30	chr6:34769066..34771587-chr6:34778054..34780112,2	K562	blood:
31	chr6:34780723..34782615-chr6:34786684..34789139,2	K562	blood:
32	chr6:34758609..34760887-chr6:34760994..34763673,2	MCF-7	breast:
33	chr6:34638321..34641038-chr6:34757399..34759050,2	K562	blood:
34	chr6:34723826..34725518-chr6:34739318..34741861,2	MCF-7	breast:
35	chr6:34772137..34774417-chr6:34775291..34779142,3	K562	blood:
36	chr6:34723754..34729214-chr6:34758122..34762652,9	MCF-7	breast:
37	chr6:34763567..34765463-chr6:34776356..34778910,2	MCF-7	breast:
38	chr6:34738626..34740977-chr6:34741967..34744356,2	K562	blood:
39	chr6:34763985..34766508-chr6:34780371..34782291,2	MCF-7	breast:
40	chr6:34736115..34738612-chr6:34739380..34741719,2	MCF-7	breast:
41	chr6:34711953..34714210-chr6:34722946..34726652,3	K562	blood:
42	chr6:34713112..34714744-chr6:34728866..34731406,2	K562	blood:
43	chr6:34765154..34767029-chr6:34793754..34796653,2	K562	blood:
44	chr6:34712098..34715933-chr6:34757940..34761251,5	MCF-7	breast:
45	chr6:34765154..34767029-chr6:34793754..34796653,2	K562	blood:
46	chr6:34755849..34757627-chr6:34758021..34759694,2	MCF-7	breast:
47	chr6:34664585..34666258-chr6:34723626..34725241,2	MCF-7	breast:
48	chr6:34707078..34708583-chr6:34711882..34714603,2	MCF-7	breast:
49	chr6:34786614..34789043-chr6:34809197..34812183,2	K562	blood:
50	chr6:34760038..34762450-chr6:35204039..35206411,2	K562	blood:

No data

(count:3 , 50 per page) page: 1

No.	miRNA target gene	miRNA name	Chromosome Location
1	SNRPC	hsa-miR-16-5p	chr6:34741398-34741418
2	SNRPC	hsa-miR-23b-3p	chr6:34741522-34741542
3	SNRPC	hsa-miR-23b-3p	chr6:34741535-34741542

Variant related genes	Relation type
ENSG00000217130	TF binding region
ENSG00000206717	TF binding region
UHRF1BP1	TF binding region
SNRPC	TF binding region
ENSG00000217130	CpG island
ENSG00000206717	CpG island
UHRF1BP1	CpG island
SNRPC	CpG island
ENSG00000196821	chromatin interactions
ENSG00000270800	chromatin interactions
ENSG00000064995	chromatin interactions
ENSG00000256690	chromatin interactions
ENSG00000162236	chromatin interactions
ENSG00000105662	chromatin interactions
ENSG00000206717	chromatin interactions
ENSG00000206538	chromatin interactions
ENSG00000217130	chromatin interactions
ENSG00000238484	chromatin interactions
ENSG00000272288	chromatin interactions
ENSG00000124562	chromatin interactions
ENSG00000065060	chromatin interactions
ENSG00000165280	chromatin interactions
ENSG00000064999	chromatin interactions
ENSG00000008324	chromatin interactions
ENSG00000124614	chromatin interactions
ENSG00000137309	chromatin interactions
ENSG00000093183	chromatin interactions
ENSG00000239059	chromatin interactions
ENSG00000170949	chromatin interactions
ENSG00000159216	chromatin interactions
ENSG00000265123	chromatin interactions
ENSG00000220643	chromatin interactions

Extended variants
information (count: 4551 )
Associated
traits (count: 106 )

Variant overlapped rSNPs/rCNVs (count:4551 , 50 per page) page: 1 2 3 4 5 6 7 ... 92

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2764211	chr6:34704613-34704614	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs552584201	chr6:34704646-34704647	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs118045171	chr6:34704672-34704673	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs535290447	chr6:34704740-34704741	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs547339801	chr6:34704775-34704776	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs368420041	chr6:34704783-34704784	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs568636335	chr6:34704788-34704789	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs536080826	chr6:34704835-34704836	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs112768741	chr6:34704840-34704841	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs141080856	chr6:34704866-34704867	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs117803861	chr6:34704877-34704878	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs76447420	chr6:34704883-34704884	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs191034883	chr6:34704902-34704903	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs149830961	chr6:34704923-34704924	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs367782663	chr6:34704997-34704998	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs115722764	chr6:34705015-34705016	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs147917737	chr6:34705016-34705017	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs561679950	chr6:34705037-34705038	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs35744142	chr6:34705042-34705043	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
20	rs2764197	chr6:34705055-34705056	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
21	rs142078885	chr6:34705095-34705096	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs561372712	chr6:34705135-34705136	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs377060973	chr6:34705138-34705139	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs6913207	chr6:34705232-34705233	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs35186650	chr6:34705239-34705240	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
26	rs182406246	chr6:34705301-34705302	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs528512892	chr6:34705310-34705311	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs375255423	chr6:34705311-34705312	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs568799086	chr6:34705397-34705398	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs535661488	chr6:34705449-34705450	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs551113787	chr6:34705451-34705452	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs369833198	chr6:34705452-34705453	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs374008338	chr6:34705483-34705484	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs187813228	chr6:34705502-34705503	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs569352283	chr6:34705524-34705525	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs2492860	chr6:34705530-34705531	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
37	rs369032024	chr6:34705544-34705545	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs557445060	chr6:34705549-34705550	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs372671503	chr6:34705572-34705573	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs566114635	chr6:34705614-34705615	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs563941812	chr6:34705638-34705639	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs532818735	chr6:34705724-34705725	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs138719656	chr6:34705736-34705737	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs555237118	chr6:34705761-34705762	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs191249286	chr6:34705780-34705781	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs544191868	chr6:34705787-34705788	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs556279964	chr6:34705788-34705789	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs577785295	chr6:34705801-34705802	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs112834650	chr6:34705830-34705831	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs570608402	chr6:34705839-34705840	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:106)

Disease	PMID	Source
Follicular lymphoma	20505157	CNVD
Glioblastoma multiforme	21080181	CNVD
Ewing''s sarcoma	21437220	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Leukemia	21518781	CNVD
Cancer	21637783	CNVD
Facial dysmorphism	22105932	CNVD
Medulloblastoma	21979893	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Endometrial cancer	22040021	CNVD
Acute myeloid leukemia	16864856	CNVD
Breast cancer	21264507	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	16751803	CNVD
Bladder cancer	19088036	CNVD
Wilms tumour	21544195	CNVD
Uveal melanoma	21693616	CNVD
Biliary cancer	19435499	CNVD
Malaria	21533027	CNVD
Retinoblastoma	19183342	CNVD
Acute myeloid leukemia	20729466	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21858162	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	21448237	CNVD
Melanoma	18172304	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Hepatocellular carcinoma	16750200	CNVD
Autism	22495311	CNVD
Cancer	16790693	CNVD
Cervical cancer	21062161	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Systemic lupus erythematosus	17503323	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Urothelial carcinoma	18382360	CNVD
Cancer	21183584	CNVD
Hodgkin''s lymphoma	17606441	CNVD
small cell lung cancer	20016488	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Gastric cancer	17908304	CNVD
Metanephric adenoma	20802469	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Schizophrenia	19571808	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Neuroblastoma	16790693	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Breast cancer	16397240	CNVD
Retinoblastoma	22278416	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Systemic lupus erythematosus	20877625	CNVD
Cleidocranial dysplasia	18696259	CNVD
Holoprosencephaly	21359414	CNVD
Liposarcoma	21253554	CNVD
Uveal melanoma	20484589	CNVD
Fibroblasts	20926602	CNVD
Systemic lupus erythematosus	19279649	CNVD
Retinoblastoma	16790693	CNVD
Acute myocardial infarction	18032375	CNVD
Renal cell carcinoma	19150565	CNVD
Systemic lupus erythematosus	19591781	CNVD
Attention deficit hyperactivity disorder	19287146	CNVD
Autism	19287146	CNVD
Erythema nodosum in leprosy	19287146	CNVD
Henoch-schoenlein purpura	19287146	CNVD
Liver cirrhosis	19287146	CNVD
Systemic lupus erythematosus	19287146	CNVD
Autoimmune disease	19135723	CNVD
Congenital adrenal hyperplasia	18478071	CNVD
Systemic lupus erythematosus	19287147	CNVD
Osteosarcoma	16790693	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Cancer	22183965	CNVD
Melanoma	22183965	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Lung cancer	18438408	CNVD
Glioblastoma multiforme	21138945	CNVD
Breast cancer	21364760	CNVD
Basal cell lymphoma	19029149	CNVD
Diffuse large b-cell lymphoma	19029149	CNVD
Myelofibrosis	22110671	CNVD
Liver carcinoma	19366792	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:3196 , 50 per page) page: 1 2 3 4 5 6 7 ... 64

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:34698000-34714000	Weak transcription	Esophagus	oesophagus
2	chr6:34699400-34707000	Weak transcription	K562	blood
3	chr6:34699800-34712200	Weak transcription	Stomach Mucosa	stomach
4	chr6:34703600-34705800	Weak transcription	HepG2	liver
5	chr6:34704400-34705000	Enhancers	ES-I3 Cell Line	embryonic stem cell
6	chr6:34704400-34705000	Enhancers	H1 Cell Line	embryonic stem cell
7	chr6:34704400-34705000	Enhancers	HUES6 Cell Line	embryonic stem cell
8	chr6:34705800-34706000	Flanking Active TSS	HepG2	liver
9	chr6:34706000-34706200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
10	chr6:34706000-34706200	Enhancers	HepG2	liver
11	chr6:34706200-34706400	Flanking Active TSS	HepG2	liver
12	chr6:34706400-34707600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
13	chr6:34706400-34712800	Enhancers	HepG2	liver
14	chr6:34707000-34708600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
15	chr6:34707000-34709000	Enhancers	Fetal Intestine Large	intestine
16	chr6:34707000-34709000	Enhancers	K562	blood
17	chr6:34707400-34708400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
18	chr6:34707400-34708400	Enhancers	Cortex derived primary cultured neurospheres	brain
19	chr6:34707400-34708600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
20	chr6:34707400-34709000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
21	chr6:34707600-34707800	Enhancers	Small Intestine	intestine
22	chr6:34707600-34708600	Enhancers	Fetal Intestine Small	intestine
23	chr6:34707600-34709000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
24	chr6:34707600-34709000	Enhancers	NHEK	skin
25	chr6:34707800-34708800	Weak transcription	Small Intestine	intestine
26	chr6:34708000-34708200	Enhancers	Hela-S3	cervix
27	chr6:34708000-34708400	Enhancers	A549	lung
28	chr6:34708200-34708400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
29	chr6:34708200-34708600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
30	chr6:34708200-34708600	Enhancers	Liver	Liver
31	chr6:34708200-34708600	Enhancers	Duodenum Mucosa	Duodenum
32	chr6:34708200-34708600	Flanking Active TSS	Hela-S3	cervix
33	chr6:34708400-34708600	Enhancers	Rectal Mucosa Donor 29	rectum
34	chr6:34708400-34712800	Weak transcription	A549	lung
35	chr6:34708600-34711200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
36	chr6:34708600-34712200	Weak transcription	Duodenum Mucosa	Duodenum
37	chr6:34708600-34712200	Weak transcription	Fetal Intestine Small	intestine
38	chr6:34708600-34712600	Weak transcription	Hela-S3	cervix
39	chr6:34708600-34713000	Weak transcription	Rectal Mucosa Donor 29	rectum
40	chr6:34708600-34713200	Weak transcription	Liver	Liver
41	chr6:34708800-34709400	Enhancers	Small Intestine	intestine
42	chr6:34708800-34711400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
43	chr6:34709000-34711200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
44	chr6:34709000-34711200	Weak transcription	NHEK	skin
45	chr6:34709000-34711600	Weak transcription	Fetal Intestine Large	intestine
46	chr6:34709000-34712800	Weak transcription	K562	blood
47	chr6:34709400-34712200	Weak transcription	Small Intestine	intestine
48	chr6:34711200-34712800	Enhancers	NHEK	skin
49	chr6:34711200-34713200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
50	chr6:34711200-34713200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin

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