Variant report

Variant	nsv885786
Chromosome Location	chr6:34426884-34542662
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2484)
CpG islands
(count:3665)
Chromatin interactive
region (count:225)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2484 , 50 per page) page: 1 2 3 4 5 6 7 ... 50

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:34485472-34485719	K562	blood:	n/a	n/a
2	ARID3A	chr6:34494652-34494762	K562	blood:	n/a	n/a
3	ARID3A	chr6:34537168-34537342	K562	blood:	n/a	n/a
4	ARID3A	chr6:34494959-34495288	HepG2	liver:	n/a	n/a
5	ARID3A	chr6:34452906-34453066	K562	blood:	n/a	n/a
6	ARID3A	chr6:34427137-34427322	HepG2	liver:	n/a	n/a
7	ARID3A	chr6:34495041-34495171	K562	blood:	n/a	n/a
8	ARID3A	chr6:34528420-34528567	HepG2	liver:	n/a	n/a
9	ARID3A	chr6:34528321-34529035	K562	blood:	n/a	n/a
10	ARID3A	chr6:34530717-34531006	K562	blood:	n/a	n/a
11	ARID3A	chr6:34535143-34535361	HepG2	liver:	n/a	n/a
12	ATF1	chr6:34530640-34531020	K562	blood:	n/a	n/a
13	ATF1	chr6:34498693-34498808	K562	blood:	n/a	n/a
14	ATF1	chr6:34528256-34528770	K562	blood:	n/a	n/a
15	ATF2	chr6:34494984-34495307	H1-hESC	embryonic stem cell:	n/a	n/a
16	ATF2	chr6:34427622-34428047	H1-hESC	embryonic stem cell:	n/a	n/a
17	ATF3	chr6:34485205-34485489	K562	blood:	n/a	n/a
18	ATF3	chr6:34458829-34459117	K562	blood:	n/a	n/a
19	ATF3	chr6:34452733-34453033	K562	blood:	n/a	n/a
20	ATF3	chr6:34433631-34433864	K562	blood:	n/a	n/a
21	BACH1	chr6:34458837-34459209	H1-hESC	embryonic stem cell:	n/a	n/a
22	BACH1	chr6:34494673-34494811	K562	blood:	n/a	n/a
23	BACH1	chr6:34458877-34459076	K562	blood:	n/a	n/a
24	BACH1	chr6:34525098-34525122	K562	blood:	n/a	n/a
25	BACH1	chr6:34528081-34528565	K562	blood:	n/a	n/a
26	BATF	chr6:34452746-34452975	GM12878	blood:	n/a	chr6:34452867-34452878
27	BCL3	chr6:34463889-34464156	GM12878	blood:	n/a	n/a
28	BCL3	chr6:34541372-34541610	GM12878	blood:	n/a	n/a
29	BCL3	chr6:34522693-34523062	GM12878	blood:	n/a	n/a
30	BCL3	chr6:34522720-34523036	GM12878	blood:	n/a	n/a
31	BCLAF1	chr6:34494974-34495328	GM12878	blood:	n/a	n/a
32	BHLHE40	chr6:34526077-34526348	K562	blood:	n/a	n/a
33	BHLHE40	chr6:34512632-34512964	K562	blood:	n/a	n/a
34	BHLHE40	chr6:34531305-34531454	K562	blood:	n/a	n/a
35	BHLHE40	chr6:34452753-34452980	GM12878	blood:	n/a	n/a
36	BHLHE40	chr6:34433443-34433930	K562	blood:	n/a	chr6:34433735-34433751
37	BHLHE40	chr6:34525097-34525230	K562	blood:	n/a	n/a
38	BHLHE40	chr6:34458903-34459141	K562	blood:	n/a	n/a
39	BHLHE40	chr6:34527683-34529135	K562	blood:	n/a	n/a
40	BHLHE40	chr6:34535812-34536294	K562	blood:	n/a	n/a
41	BHLHE40	chr6:34494998-34495331	K562	blood:	n/a	n/a
42	BHLHE40	chr6:34498559-34498914	K562	blood:	n/a	n/a
43	BHLHE40	chr6:34436208-34436550	GM12878	blood:	n/a	n/a
44	BHLHE40	chr6:34427751-34427973	GM12878	blood:	n/a	n/a
45	BHLHE40	chr6:34452706-34452850	K562	blood:	n/a	n/a
46	BHLHE40	chr6:34481627-34482576	K562	blood:	n/a	n/a
47	BHLHE40	chr6:34440239-34440572	K562	blood:	n/a	n/a
48	BHLHE40	chr6:34530292-34531071	K562	blood:	n/a	n/a
49	BHLHE40	chr6:34535821-34536274	HepG2	liver:	n/a	n/a
50	BHLHE40	chr6:34528358-34529016	HepG2	liver:	n/a	n/a

(count:3665 , 50 per page) page: 1 2 3 4 5 6 7 ... 74

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:34434017-34434067	SK-N-MC	brain:	n/a
2	chr6:34504890-34504940	GM19239	blood:	n/a
3	chr6:34434017-34434067	T-47D	breast:	n/a
4	chr6:34498714-34498764	BJ	skin:	n/a
5	chr6:34495124-34495174	AG04450	lung:	fetal
6	chr6:34434017-34434067	SK-N-MC	brain:	n/a
7	chr6:34504890-34504940	GM19239	blood:	n/a
8	chr6:34434017-34434067	T-47D	breast:	n/a
9	chr6:34498714-34498764	BJ	skin:	n/a
10	chr6:34495124-34495174	AG04450	lung:	fetal
11	chr6:34528827-34528877	HUVEC	blood vessel:	n/a
12	chr6:34498714-34498764	HCPEpiC	choroid plexus:	n/a
13	chr6:34524597-34524647	HRCEpiC	kidney:	n/a
14	chr6:34504890-34504940	ECC-1	luminal epithelium:	n/a
15	chr6:34523925-34523975	LNCaP	prostate:	n/a
16	chr6:34523925-34523975	HRCEpiC	kidney:	n/a
17	chr6:34495054-34495104	ECC-1	luminal epithelium:	n/a
18	chr6:34433320-34433370	H1-hESC	embryonic stem cell:	embryo
19	chr6:34495292-34495342	NH-A	brain:	n/a
20	chr6:34502119-34502169	IMR90	lung:	fetal
21	chr6:34499389-34499439	PrEC	prostate:	n/a
22	chr6:34498714-34498764	HRCEpiC	kidney:	n/a
23	chr6:34508820-34508870	PFSK-1	brain:	n/a
24	chr6:34434842-34434892	K562	blood:	n/a
25	chr6:34433320-34433370	NH-A	brain:	n/a
26	chr6:34458902-34458952	AG09309	skin:	n/a
27	chr6:34512215-34512265	MCF-7	breast:	n/a
28	chr6:34511514-34511564	NH-A	brain:	n/a
29	chr6:34512215-34512265	PrEC	prostate:	n/a
30	chr6:34458902-34458952	Hela-S3	cervix:	n/a
31	chr6:34434017-34434067	ovcar-3	ovarian:	n/a
32	chr6:34524597-34524647	HCM	heart:	n/a
33	chr6:34502119-34502169	AG10803	skin:	n/a
34	chr6:34437227-34437277	HPAEpiC	pulmonary alveolar:	n/a
35	chr6:34499488-34499538	SK-N-SH_RA	brain:	n/a
36	chr6:34524095-34524145	AG10803	skin:	n/a
37	chr6:34433713-34433763	NB4	blood:	n/a
38	chr6:34486129-34486179	ProgFib	skin:	n/a
39	chr6:34482479-34482529	SAEC	small airway:	n/a
40	chr6:34499488-34499538	HRE	kidney:	n/a
41	chr6:34524097-34524147	T-47D	breast:	n/a
42	chr6:34499504-34499554	HepG2	liver:	n/a
43	chr6:34495292-34495342	AG04450	lung:	fetal
44	chr6:34512215-34512265	HEK293	kidney:	embryo
45	chr6:34495393-34495443	HRPEpiC	eye:	n/a
46	chr6:34434076-34434126	RPTEC	kidney:	n/a
47	chr6:34524597-34524647	AG10803	skin:	n/a
48	chr6:34524766-34524816	SK-N-SH	brain:	n/a
49	chr6:34486129-34486179	HMEC	breast:	n/a
50	chr6:34495292-34495342	HNPCEpiC	eye:	n/a

(count:225 , 50 per page) page: 1 2 3 4 5

No.	Distal block	Cell Line	Cell type
1	chr6:34486477..34488245-chr6:34492452..34495163,2	MCF-7	breast:
2	chr6:34426702..34428652-chr6:34520960..34523550,2	MCF-7	breast:
3	chr6:34495305..34497309-chr6:34500179..34501973,2	K562	blood:
4	chr6:34484087..34487534-chr6:34488647..34495126,10	K562	blood:
5	chr6:34439648..34441569-chr6:34446146..34448661,2	K562	blood:
6	chr6:34441851..34443719-chr6:34445470..34448449,2	K562	blood:
7	chr6:34427418..34428084-chr6:34497140..34498209,3	MCF-7	breast:
8	chr6:34522370..34525112-chr6:34541822..34544372,2	MCF-7	breast:
9	chr6:34496034..34498791-chr6:34510835..34512433,2	K562	blood:
10	chr6:34478801..34480566-chr6:34489552..34491373,2	K562	blood:
11	chr6:34440406..34442215-chr6:34442731..34445360,2	MCF-7	breast:
12	chr6:34514736..34516500-chr6:34519380..34521095,2	K562	blood:
13	chr6:34494469..34496151-chr6:34577655..34579267,2	K562	blood:
14	chr6:34467900..34469881-chr6:34479800..34481611,2	K562	blood:
15	chr6:34528409..34535112-chr6:34539790..34543716,10	K562	blood:
16	chr6:34509583..34511363-chr6:34518250..34520010,2	K562	blood:
17	chr6:34480102..34483166-chr6:34493351..34495807,3	MCF-7	breast:
18	chr6:34494545..34497462-chr6:34498275..34503019,6	MCF-7	breast:
19	chr6:34426702..34428652-chr6:34520960..34523550,2	MCF-7	breast:
20	chr6:34193853..34195785-chr6:34492922..34495154,2	K562	blood:
21	chr6:34503128..34505845-chr6:34536309..34539232,2	K562	blood:
22	chr6:34216270..34217861-chr6:34527614..34529829,2	MCF-7	breast:
23	chr6:34440695..34443428-chr6:34457495..34459339,2	MCF-7	breast:
24	chr6:34536153..34538160-chr6:34545936..34548526,2	MCF-7	breast:
25	chr6:34207322..34209425-chr6:34465568..34467978,2	K562	blood:
26	chr6:34501585..34503222-chr6:34504276..34506644,2	K562	blood:
27	chr6:34462336..34465080-chr6:34471229..34474153,4	K562	blood:
28	chr6:34502047..34504010-chr6:34512836..34514494,2	K562	blood:
29	chr6:34467900..34469881-chr6:34479800..34481611,2	K562	blood:
30	chr6:34494680..34495634-chr6:34577124..34578035,2	MCF-7	breast:
31	chr6:34497199..34497799-chr6:34557125..34558123,2	MCF-7	breast:
32	chr6:34427383..34427978-chr6:34528004..34528902,2	MCF-7	breast:
33	chr6:34439690..34441668-chr6:34462680..34464330,2	K562	blood:
34	chr6:34494038..34495878-chr6:34511727..34514586,2	K562	blood:
35	chr6:34503783..34506203-chr6:34577530..34580135,3	MCF-7	breast:
36	chr6:34532465..34535112-chr6:34540040..34542974,2	K562	blood:
37	chr6:34522438..34524089-chr6:34549801..34552822,3	MCF-7	breast:
38	chr6:34496932..34498060-chr6:34528153..34529212,4	MCF-7	breast:
39	chr6:34535124..34537027-chr6:34540257..34543237,2	K562	blood:
40	chr6:34440406..34442215-chr6:34442731..34445360,2	MCF-7	breast:
41	chr6:34508152..34511012-chr6:34535080..34537020,2	K562	blood:
42	chr6:34528409..34535112-chr6:34539790..34543716,10	K562	blood:
43	chr6:34462776..34465080-chr6:34471229..34474153,3	K562	blood:
44	chr18:50300436..50303454-chr6:34521553..34523812,3	MCF-7	breast:
45	chr6:34427418..34428084-chr6:34497140..34498209,3	MCF-7	breast:
46	chr6:34494831..34497738-chr6:34508657..34510396,2	MCF-7	breast:
47	chr6:34495679..34498360-chr6:34503054..34505628,3	MCF-7	breast:
48	chr6:34478801..34480566-chr6:34489552..34491373,2	K562	blood:
49	chr6:34506980..34511719-chr6:34518115..34520438,4	K562	blood:
50	chr6:34514809..34519137-chr6:34522826..34525341,4	K562	blood:

No data

Variant related genes	Relation type
SPDEF	TF binding region
ENSG00000221635	TF binding region
PACSIN1	TF binding region
SPDEF	CpG island
ENSG00000221635	CpG island
PACSIN1	CpG island
ENSG00000221635	chromatin interactions
ENSG00000204257	chromatin interactions
ENSG00000124664	chromatin interactions
ENSG00000177885	chromatin interactions
ENSG00000223837	chromatin interactions
ENSG00000270800	chromatin interactions
ENSG00000272288	chromatin interactions
ENSG00000137309	chromatin interactions
ENSG00000196821	chromatin interactions
ENSG00000265342	chromatin interactions
ENSG00000196114	chromatin interactions
ENSG00000124614	chromatin interactions
ENSG00000186577	chromatin interactions
ENSG00000204256	chromatin interactions
ENSG00000065060	chromatin interactions
ENSG00000124507	chromatin interactions

Extended variants
information (count: 4752 )
Associated
traits (count: 107 )

Variant overlapped rSNPs/rCNVs (count:4752 , 50 per page) page: 1 2 3 4 5 6 7 ... 96

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs9394223	chr6:34426884-34426885	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs144752079	chr6:34426914-34426915	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs577722001	chr6:34426915-34426916	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs183140390	chr6:34427006-34427007	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs4713793	chr6:34427026-34427027	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs527616012	chr6:34427038-34427039	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs375278930	chr6:34427041-34427042	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs549129366	chr6:34427084-34427085	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs560950274	chr6:34427088-34427089	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs529343720	chr6:34427170-34427171	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs145337113	chr6:34427224-34427225	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs549524665	chr6:34427225-34427226	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs550671568	chr6:34427233-34427234	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs539455920	chr6:34427235-34427236	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs55853693	chr6:34427236-34427237	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs188188321	chr6:34427266-34427267	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs539446240	chr6:34427276-34427277	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs551389497	chr6:34427305-34427306	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs147476638	chr6:34427337-34427338	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs4713794	chr6:34427347-34427348	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs9394224	chr6:34427354-34427355	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs546928748	chr6:34427372-34427373	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs537898624	chr6:34427384-34427385	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs368967046	chr6:34427401-34427402	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs192258757	chr6:34427440-34427441	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs577857703	chr6:34427484-34427485	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs118174856	chr6:34427542-34427543	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs559925462	chr6:34427543-34427544	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs572279461	chr6:34427571-34427572	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs542562818	chr6:34427603-34427604	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs561099534	chr6:34427606-34427607	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs184408428	chr6:34427693-34427694	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs148511570	chr6:34427725-34427726	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs562621078	chr6:34427777-34427778	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs73405660	chr6:34427793-34427794	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs551719323	chr6:34427805-34427806	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs566773446	chr6:34427879-34427880	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs187937833	chr6:34427938-34427939	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs192351876	chr6:34427949-34427950	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs567989211	chr6:34427959-34427960	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs185667176	chr6:34427971-34427972	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs576078217	chr6:34427990-34427991	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs556820490	chr6:34427992-34427993	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs577794524	chr6:34428066-34428067	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs538763385	chr6:34428108-34428109	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs553684186	chr6:34428120-34428121	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs571958703	chr6:34428141-34428142	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs542650432	chr6:34428150-34428151	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs554565673	chr6:34428285-34428286	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs142751636	chr6:34428348-34428349	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:107)

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
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Amyotrophic lateral sclerosis	20685689	CNVD

Chromatin state (count:2154 , 50 per page) page: 1 2 3 4 5 6 7 ... 44

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:34394400-34433200	Weak transcription	Right Atrium	heart
2	chr6:34417600-34428000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
3	chr6:34425000-34429000	Weak transcription	HUES48 Cell Line	embryonic stem cell
4	chr6:34425600-34428000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
5	chr6:34425600-34429000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
6	chr6:34426000-34428000	Weak transcription	H1 Cell Line	embryonic stem cell
7	chr6:34426000-34430400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
8	chr6:34426000-34430400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
9	chr6:34426400-34430000	Weak transcription	HUES6 Cell Line	embryonic stem cell
10	chr6:34426600-34428600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
11	chr6:34426600-34429400	Weak transcription	K562	blood
12	chr6:34426600-34430200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
13	chr6:34426800-34428200	Enhancers	HepG2	liver
14	chr6:34427400-34428000	Enhancers	Liver	Liver
15	chr6:34427800-34428200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
16	chr6:34427800-34428200	Enhancers	Stomach Mucosa	stomach
17	chr6:34428000-34428200	Enhancers	ES-I3 Cell Line	embryonic stem cell
18	chr6:34428000-34428800	Enhancers	A549	lung
19	chr6:34428000-34429000	Enhancers	iPS-15b Cell Line	embryonic stem cell
20	chr6:34428000-34429200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
21	chr6:34428000-34429200	Enhancers	NHEK	skin
22	chr6:34428000-34430200	Weak transcription	Liver	Liver
23	chr6:34428000-34432200	Enhancers	H1 Cell Line	embryonic stem cell
24	chr6:34428200-34428600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
25	chr6:34428200-34428600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
26	chr6:34428200-34430000	Weak transcription	HepG2	liver
27	chr6:34428200-34430400	Weak transcription	Stomach Mucosa	stomach
28	chr6:34428600-34428800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
29	chr6:34428600-34429200	Enhancers	ES-I3 Cell Line	embryonic stem cell
30	chr6:34428600-34429200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
31	chr6:34428600-34429200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
32	chr6:34428600-34429200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
33	chr6:34428600-34429200	Enhancers	HMEC	breast
34	chr6:34428600-34429400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
35	chr6:34428800-34429000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
36	chr6:34428800-34429000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
37	chr6:34428800-34429000	Enhancers	iPS-18 Cell Line	embryonic stem cell
38	chr6:34428800-34429000	Enhancers	iPS-20b Cell Line	embryonic stem cell
39	chr6:34428800-34429200	Enhancers	H9 Cell Line	embryonic stem cell
40	chr6:34428800-34429400	Enhancers	HUVEC	blood vessel
41	chr6:34428800-34429800	Weak transcription	A549	lung
42	chr6:34428800-34433200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
43	chr6:34429000-34429200	Enhancers	HUES48 Cell Line	embryonic stem cell
44	chr6:34429000-34430000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
45	chr6:34429000-34430000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
46	chr6:34429000-34430400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
47	chr6:34429000-34430800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
48	chr6:34429200-34430000	Weak transcription	HUES48 Cell Line	embryonic stem cell
49	chr6:34429200-34430200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
50	chr6:34429200-34430200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin

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