Variant report

Variant	nsv884104
Chromosome Location	chr6:30740680-30753146
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:593)
CpG islands
(count:61)
Chromatin interactive
region (count:35)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:593 , 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	chr6:30749425-30750806	HepG2	liver:	n/a	n/a
2	ARID3A	chr6:30749571-30750337	K562	blood:	n/a	n/a
3	ATF1	chr6:30749451-30750290	K562	blood:	n/a	chr6:30749808-30749822
4	ATF2	chr6:30749467-30750091	GM12878	blood:	n/a	chr6:30749808-30749822
5	ATF2	chr6:30749323-30750278	GM12878	blood:	n/a	chr6:30749808-30749822
6	ATF3	chr6:30749499-30749934	K562	blood:	n/a	n/a
7	ATF3	chr6:30749273-30750308	K562	blood:	n/a	n/a
8	ATF3	chr6:30749384-30750697	A549	lung:	n/a	n/a
9	ATF3	chr6:30749244-30750106	A549	lung:	n/a	n/a
10	BATF	chr6:30749650-30749929	GM12878	blood:	n/a	n/a
11	BCL3	chr6:30749287-30750863	A549	lung:	n/a	chr6:30749933-30749942
12	BCL3	chr6:30749469-30750912	A549	lung:	n/a	chr6:30749933-30749942
13	BCLAF1	chr6:30749604-30750150	GM12878	blood:	n/a	chr6:30749933-30749942
14	BHLHE40	chr6:30749429-30750051	K562	blood:	n/a	n/a
15	BHLHE40	chr6:30749446-30749960	HepG2	liver:	n/a	n/a
16	BRCA1	chr6:30749567-30750003	HepG2	liver:	n/a	n/a
17	BRCA1	chr6:30749278-30750153	Hela-S3	cervix:	n/a	n/a
18	CBX3	chr6:30748316-30748730	K562	blood:	n/a	n/a
19	CBX3	chr6:30749027-30750524	K562	blood:	n/a	n/a
20	CCNT2	chr6:30749660-30750078	K562	blood:	n/a	n/a
21	CEBPB	chr6:30749460-30750092	ECC-1	luminal epithelium:	n/a	chr6:30749779-30749790
22	CEBPB	chr6:30750508-30750777	K562	blood:	n/a	chr6:30750630-30750641
23	CEBPB	chr6:30746919-30747099	H1-hESC	embryonic stem cell:	n/a	n/a
24	CEBPB	chr6:30742856-30743187	HepG2	liver:	n/a	chr6:30743008-30743019
25	CEBPB	chr6:30750250-30750904	A549	lung:	n/a	chr6:30750630-30750641
26	CEBPB	chr6:30746877-30747199	K562	blood:	n/a	n/a
27	CEBPB	chr6:30746779-30747233	K562	blood:	n/a	n/a
28	CEBPB	chr6:30749251-30750822	IMR90	lung:	n/a	chr6:30750630-30750641 chr6:30749779-30749790
29	CEBPB	chr6:30750435-30750826	HepG2	liver:	n/a	chr6:30750630-30750641
30	CEBPB	chr6:30751315-30751516	K562	blood:	n/a	n/a
31	CEBPB	chr6:30749160-30750886	A549	lung:	n/a	chr6:30750630-30750641 chr6:30749779-30749790
32	CEBPB	chr6:30749265-30750087	HepG2	liver:	n/a	chr6:30749779-30749790
33	CEBPB	chr6:30750233-30750925	ECC-1	luminal epithelium:	n/a	chr6:30750630-30750641
34	CEBPB	chr6:30742888-30743171	HepG2	liver:	n/a	chr6:30743008-30743019
35	CEBPB	chr6:30742964-30743080	A549	lung:	n/a	chr6:30743008-30743019
36	CEBPB	chr6:30749511-30750085	MCF-7	breast:	n/a	chr6:30749779-30749790
37	CEBPB	chr6:30751303-30751488	H1-hESC	embryonic stem cell:	n/a	n/a
38	CEBPB	chr6:30749210-30750909	HCT-116	colon:	n/a	chr6:30750630-30750641 chr6:30749779-30749790
39	CEBPB	chr6:30746856-30747396	ECC-1	luminal epithelium:	n/a	n/a
40	CEBPB	chr6:30749485-30750808	HepG2	liver:	n/a	chr6:30750630-30750641 chr6:30749779-30749790
41	CEBPB	chr6:30749210-30750894	Hela-S3	cervix:	n/a	chr6:30750630-30750641 chr6:30749779-30749790
42	CEBPB	chr6:30746878-30747145	IMR90	lung:	n/a	n/a
43	CEBPB	chr6:30750251-30750835	ECC-1	luminal epithelium:	n/a	chr6:30750630-30750641
44	CEBPB	chr6:30745665-30745822	A549	lung:	n/a	n/a
45	CEBPB	chr6:30751221-30751509	HepG2	liver:	n/a	n/a
46	CEBPB	chr6:30748723-30748842	HepG2	liver:	n/a	n/a
47	CEBPB	chr6:30745656-30745870	HepG2	liver:	n/a	n/a
48	CEBPB	chr6:30751303-30751500	HepG2	liver:	n/a	n/a
49	CEBPB	chr6:30749070-30750972	HCT-116	colon:	n/a	chr6:30750630-30750641 chr6:30749779-30749790
50	CEBPB	chr6:30750467-30750729	H1-hESC	embryonic stem cell:	n/a	chr6:30750630-30750641

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:30749279-30749329	PFSK-1	brain:	n/a
2	chr6:30749279-30749329	HMEC	breast:	n/a
3	chr6:30749279-30749329	HIPEpiC	eye:	n/a
4	chr6:30749279-30749329	SK-N-SH	brain:	n/a
5	chr6:30749279-30749329	BE2_C	brain:	n/a
6	chr6:30749279-30749329	HAEpiC	amniotic membrane:	n/a
7	chr6:30749279-30749329	NH-A	brain:	n/a
8	chr6:30749279-30749329	HCT-116	colon:	n/a
9	chr6:30749279-30749329	HRE	kidney:	n/a
10	chr6:30749279-30749329	GM19239	blood:	n/a
11	chr6:30749279-30749329	GM12892	blood:	n/a
12	chr6:30749279-30749329	BJ	skin:	n/a
13	chr6:30749279-30749329	HRPEpiC	eye:	n/a
14	chr6:30749279-30749329	SK-N-MC	brain:	n/a
15	chr6:30749279-30749329	HPAEpiC	pulmonary alveolar:	n/a
16	chr6:30749279-30749329	GM12891	blood:	n/a
17	chr6:30749279-30749329	NT2-D1	testis:	n/a
18	chr6:30749279-30749329	IMR90	lung:	fetal
19	chr6:30749279-30749329	RPTEC	kidney:	n/a
20	chr6:30749279-30749329	T-47D	breast:	n/a
21	chr6:30749279-30749329	HEK293	kidney:	embryo
22	chr6:30749279-30749329	SK-N-SH_RA	brain:	n/a
23	chr6:30749279-30749329	H1-hESC	embryonic stem cell:	embryo
24	chr6:30749279-30749329	NHDF-neo	bronchial:	n/a
25	chr6:30749279-30749329	NB4	blood:	n/a
26	chr6:30749279-30749329	HCF	heart:	n/a
27	chr6:30749279-30749329	MCF-7	breast:	n/a
28	chr6:30749279-30749329	AG04450	lung:	fetal
29	chr6:30749279-30749329	GM06990	blood:	n/a
30	chr6:30749279-30749329	SKMC	muscle:	n/a
31	chr6:30749279-30749329	U87	brain:	n/a
32	chr6:30749279-30749329	AG09319	gingival:	n/a
33	chr6:30749279-30749329	Hepatocyte	liver:	n/a
34	chr6:30749279-30749329	CMK	blood:	n/a
35	chr6:30749279-30749329	ovcar-3	ovarian:	n/a
36	chr6:30749279-30749329	AoSMC	blood vessel:	n/a
37	chr6:30749279-30749329	HEEpiC	esophagus:	n/a
38	chr6:30749279-30749329	Hela-S3	cervix:	n/a
39	chr6:30749279-30749329	SAEC	small airway:	n/a
40	chr6:30749279-30749329	ECC-1	luminal epithelium:	n/a
41	chr6:30749279-30749329	PrEC	prostate:	n/a
42	chr6:30749279-30749329	Caco-2	colon:	n/a
43	chr6:30749279-30749329	LNCaP	prostate:	n/a
44	chr6:30749279-30749329	HepG2	liver:	n/a
45	chr6:30749279-30749329	GM12878	blood:	n/a
46	chr6:30749279-30749329	AG09309	skin:	n/a
47	chr6:30749279-30749329	HRCEpiC	kidney:	n/a
48	chr6:30749279-30749329	HCPEpiC	choroid plexus:	n/a
49	chr6:30749279-30749329	A549	lung:	n/a
50	chr6:30749279-30749329	HNPCEpiC	eye:	n/a

(count:35 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:30746239..30748056-chr6:30850531..30852565,3	MCF-7	breast:
2	chr6:30705811..30713504-chr6:30753060..30768565,33	MCF-7	breast:
3	chr15:64994923..64995558-chr6:30748917..30749642,2	Hela-S3	cervix:
4	chr6:30709062..30712759-chr6:30740539..30742608,4	K562	blood:
5	chr6:30694210..30695985-chr6:30745346..30747310,2	K562	blood:
6	chr6:30648927..30651629-chr6:30742930..30745365,2	K562	blood:
7	chr6:30739130..30742242-chr6:30780166..30782431,3	K562	blood:
8	chr6:30719384..30720067-chr6:30747678..30748455,3	MCF-7	breast:
9	chr6:30753093..30755671-chr6:30782246..30783854,2	K562	blood:
10	chr6:30742016..30748001-chr6:30748066..30750476,5	MCF-7	breast:
11	chr6:30713953..30715513-chr6:30740306..30742825,2	K562	blood:
12	chr6:30738970..30741977-chr6:30793706..30796488,3	MCF-7	breast:
13	chr6:30687429..30690376-chr6:30739230..30741789,3	K562	blood:
14	chr6:30649121..30651445-chr6:30738828..30742388,3	K562	blood:
15	chr6:30739945..30741810-chr6:30780568..30783125,2	K562	blood:
16	chr6:30750359..30753448-chr6:30757734..30761171,4	MCF-7	breast:
17	chr6:30613838..30616795-chr6:30748344..30751338,2	K562	blood:
18	chr6:30747932..30749847-chr6:30861062..30862984,2	K562	blood:
19	chr6:30583226..30586077-chr6:30737832..30742122,4	K562	blood:
20	chr6:30742999..30744721-chr6:30782116..30783840,2	MCF-7	breast:
21	chr6:30750458..30752219-chr6:30756523..30759247,2	MCF-7	breast:
22	chr6:30583409..30587215-chr6:30748473..30750740,4	K562	blood:
23	chr6:30710424..30713995-chr6:30746295..30752430,9	K562	blood:
24	chr6:30748758..30751430-chr6:30850690..30852588,5	MCF-7	breast:
25	chr6:30652005..30653974-chr6:30752044..30754384,2	K562	blood:
26	chr6:30744501..30746062-chr6:30781081..30782628,2	K562	blood:
27	chr6:30685130..30687169-chr6:30748703..30751412,3	K562	blood:
28	chr6:30745917..30748118-chr6:30776110..30778177,2	K562	blood:
29	chr6:30748393..30749996-chr6:30841265..30843895,2	K562	blood:
30	chr6:30657201..30658778-chr6:30748296..30750541,2	K562	blood:
31	chr6:30749778..30751326-chr6:30778307..30780023,3	MCF-7	breast:
32	chr6:30725912..30728357-chr6:30744418..30747133,2	K562	blood:
33	chr6:30735125..30737471-chr6:30740402..30742755,2	MCF-7	breast:
34	chr6:30752526..30755713-chr6:30784163..30787914,3	MCF-7	breast:
35	chr6:27100755..27102737-chr6:30749085..30751315,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TUBB-13	chr6:30749735-30749903	ENSG00000228022

No data

Variant related genes	Relation type
HCG20	TF binding region
HCG20	CpG island
ENSG00000196787	chromatin interactions
ENSG00000196230	chromatin interactions
ENSG00000180304	chromatin interactions
ENSG00000204580	chromatin interactions
ENSG00000228022	chromatin interactions
ENSG00000137404	chromatin interactions
ENSG00000204569	chromatin interactions
ENSG00000137331	chromatin interactions
ENSG00000237775	chromatin interactions
ENSG00000222894	chromatin interactions
ENSG00000204568	chromatin interactions
ENSG00000266183	chromatin interactions
ENSG00000137312	chromatin interactions
ENSG00000137337	chromatin interactions
ENSG00000272273	chromatin interactions
ENSG00000204564	chromatin interactions

Extended variants
information (count: 399 )
Associated
traits (count: 122 )

Variant overlapped rSNPs/rCNVs (count:399 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs16897889	chr6:30740680-30740681	Weak transcription Enhancers	Chromatin interactive region	7 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs556584342	chr6:30740743-30740744	Weak transcription Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
3	rs568537084	chr6:30740785-30740786	Weak transcription Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
4	rs61155723	chr6:30740830-30740831	Weak transcription Enhancers	Chromatin interactive region	7 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs529788892	chr6:30740834-30740835	Weak transcription Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
6	rs141056165	chr6:30740846-30740847	Weak transcription Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
7	rs567903811	chr6:30740901-30740902	Weak transcription Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
8	rs144904672	chr6:30740916-30740917	Weak transcription Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
9	rs73425709	chr6:30740919-30740920	Weak transcription Enhancers	Chromatin interactive region	7 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs566997479	chr6:30741103-30741104	Weak transcription Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
11	rs199728742	chr6:30741131-30741132	Weak transcription Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
12	rs3132604	chr6:30741226-30741227	Weak transcription Enhancers	Chromatin interactive region	7 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
13	rs559058137	chr6:30741235-30741236	Weak transcription Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
14	rs575555791	chr6:30741247-30741248	Weak transcription Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
15	rs368038260	chr6:30741259-30741260	Weak transcription Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
16	rs544545837	chr6:30741276-30741277	Weak transcription Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
17	rs372293429	chr6:30741280-30741281	Weak transcription Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
18	rs3095335	chr6:30741305-30741306	Weak transcription Enhancers	Chromatin interactive region	7 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
19	rs540072883	chr6:30741335-30741336	Weak transcription Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
20	rs569316333	chr6:30741366-30741367	Weak transcription Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
21	rs5875272	chr6:30741374-30741375	Weak transcription Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
22	rs368485463	chr6:30741377-30741378	Weak transcription Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
23	rs559896270	chr6:30741415-30741416	Weak transcription Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
24	rs182513928	chr6:30741431-30741432	Weak transcription Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
25	rs545512654	chr6:30741450-30741451	Weak transcription Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
26	rs187914867	chr6:30741492-30741493	Weak transcription Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
27	rs75433398	chr6:30741528-30741529	Weak transcription Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
28	rs531210735	chr6:30741570-30741571	Weak transcription Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
29	rs548167288	chr6:30741577-30741578	Weak transcription Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
30	rs573150002	chr6:30741584-30741585	Weak transcription Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
31	rs190755699	chr6:30741645-30741646	Enhancers Weak transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
32	rs534494219	chr6:30741669-30741670	Enhancers Weak transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
33	rs142119719	chr6:30741740-30741741	Enhancers Weak transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
34	rs372843100	chr6:30741794-30741795	Enhancers Weak transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
35	rs184239022	chr6:30741978-30741979	Enhancers Weak transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
36	rs188689284	chr6:30742013-30742014	Enhancers Weak transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
37	rs552705070	chr6:30742104-30742105	Enhancers Weak transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
38	rs151157703	chr6:30742126-30742127	Enhancers Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
39	rs571351388	chr6:30742131-30742132	Enhancers Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
40	rs4248148	chr6:30742134-30742135	Enhancers Weak transcription	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs116763020	chr6:30742141-30742142	Enhancers Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
42	rs574673572	chr6:30742143-30742144	Enhancers Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
43	rs533859237	chr6:30742174-30742175	Enhancers Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
44	rs553617953	chr6:30742192-30742193	Enhancers Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
45	rs192240469	chr6:30742197-30742198	Enhancers Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
46	rs545547476	chr6:30742219-30742220	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
47	rs140288776	chr6:30742285-30742286	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
48	rs576078558	chr6:30742286-30742287	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
49	rs541487424	chr6:30742287-30742288	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
50	rs184393552	chr6:30742335-30742336	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:122)

Disease	PMID	Source
Acute lymphoblastic leukemia	22237106	CNVD
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
Lung cancer	18438408	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	21448237	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Cancer	20164919	CNVD
Melanoma	18172304	CNVD
Breast cancer	22844521	CNVD
HIV/AIDS	22844521	CNVD
Ovarian cancer	22844521	CNVD
Prostate cancer	22844521	CNVD
Psoriasis	22844521	CNVD
Rheumatoid arthritis	22844521	CNVD
Sclerosis systemic	22844521	CNVD
Systemic lupus erythematosus	22844521	CNVD
Breast cancer	22522925	CNVD
Ovarian cancer	21781307	CNVD
Breast cancer	21552322	CNVD
Immune disease	21076436	CNVD
Autoimmune disease	19135723	CNVD
Systemic lupus erythematosus	17953491	CNVD
Recurrent Infections	22737222	CNVD
Systemic lupus erythematosus	21904924	CNVD
Ependymoma	19289631	CNVD
Gestational infection	22844521	CNVD
Head circumference	22844521	CNVD
Infertility	22844521	CNVD
Recurrent birth weight diabetes	22844521	CNVD
Obesity	22844521	CNVD
Recurrent pregnancy loss	22844521	CNVD
Intellectual disability	21811512	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Congenital anomalies of the kidney and urinary tract	18694510	CNVD
Nasopharyngeal cancer	22815911	CNVD
Hepatocellular carcinoma	16750200	CNVD
Basal cell lymphoma	21115979	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Autism	22495311	CNVD
Cancer	16790693	CNVD
Cervical cancer	21062161	CNVD
Breast cancer	21785460	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
Renal cell carcinoma	18765545	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
abnormal development	18461090	CNVD
Melanoma	17363583	CNVD
Myelofibrosis	22110671	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
Breast cancer	21364760	CNVD
Lung cancer	21569311	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
Congenital adrenal hyperplasia	18478071	CNVD
Systemic lupus erythematosus	19287147	CNVD
Osteosarcoma	16790693	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD

Chromatin state (count:628 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:30734800-30747400	Weak transcription	Liver	Liver
2	chr6:30737600-30742400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr6:30737600-30742400	Weak transcription	Fetal Muscle Trunk	muscle
4	chr6:30737600-30742400	Weak transcription	Left Ventricle	heart
5	chr6:30737600-30744200	Weak transcription	Sigmoid Colon	Sigmoid Colon
6	chr6:30737600-30746000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
7	chr6:30737600-30746000	Weak transcription	Fetal Lung	lung
8	chr6:30737600-30746000	Weak transcription	Gastric	stomach
9	chr6:30737600-30746000	Weak transcription	Lung	lung
10	chr6:30737600-30746000	Weak transcription	Pancreas	Pancrea
11	chr6:30737600-30746000	Weak transcription	Right Atrium	heart
12	chr6:30737600-30746000	Weak transcription	Right Ventricle	heart
13	chr6:30737600-30746000	Weak transcription	Spleen	Spleen
14	chr6:30737600-30746200	Weak transcription	Psoas Muscle	Psoas
15	chr6:30737600-30746600	Weak transcription	Aorta	Aorta
16	chr6:30737600-30749200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
17	chr6:30738000-30741600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
18	chr6:30738000-30741800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
19	chr6:30738000-30742400	Weak transcription	Fetal Muscle Leg	muscle
20	chr6:30738000-30742400	Weak transcription	Skeletal Muscle Female	skeletal muscle
21	chr6:30738000-30746000	Weak transcription	Colon Smooth Muscle	Colon
22	chr6:30738000-30746400	Weak transcription	Esophagus	oesophagus
23	chr6:30738200-30741600	Weak transcription	H9 Cell Line	embryonic stem cell
24	chr6:30738200-30741800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
25	chr6:30738200-30742000	Weak transcription	Fetal Heart	heart
26	chr6:30738200-30742000	Weak transcription	Skeletal Muscle Male	skeletal muscle
27	chr6:30738200-30742400	Weak transcription	Placenta	Placenta
28	chr6:30738200-30742600	Weak transcription	HSMM	muscle
29	chr6:30738200-30745200	Weak transcription	Primary T cells fromperipheralblood	blood
30	chr6:30738400-30747000	Weak transcription	HUES64 Cell Line	embryonic stem cell
31	chr6:30738600-30741600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
32	chr6:30738600-30741800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
33	chr6:30738600-30742400	Weak transcription	Stomach Smooth Muscle	stomach
34	chr6:30738600-30743000	Weak transcription	NHLF	lung
35	chr6:30738600-30745800	Weak transcription	NH-A	brain
36	chr6:30738600-30746000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
37	chr6:30738600-30746000	Weak transcription	Muscle Satellite Cultured Cells	--
38	chr6:30738600-30747000	Weak transcription	HUES6 Cell Line	embryonic stem cell
39	chr6:30738600-30749200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
40	chr6:30738800-30742400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
41	chr6:30738800-30742600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
42	chr6:30738800-30742600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
43	chr6:30738800-30744600	Weak transcription	Fetal Thymus	thymus
44	chr6:30738800-30746200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
45	chr6:30738800-30746800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
46	chr6:30739000-30741800	Weak transcription	HSMMtube	muscle
47	chr6:30739000-30742400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
48	chr6:30739000-30742400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
49	chr6:30739000-30742400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
50	chr6:30739000-30742400	Weak transcription	NHDF-Ad	bronchial

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