Variant report

Variant	nsv437523
Chromosome Location	chr6:119251971-119260280
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:531)
CpG islands
(count:551)
Chromatin interactive
region (count:35)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:531 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:119255836-119256036	HepG2	liver:	n/a	n/a
2	ATF2	chr6:119255596-119256233	GM12878	blood:	n/a	n/a
3	BCLAF1	chr6:119255934-119256470	GM12878	blood:	n/a	chr6:119256194-119256207
4	BHLHE40	chr6:119255476-119256552	GM12878	blood:	n/a	n/a
5	BHLHE40	chr6:119255367-119256535	HepG2	liver:	n/a	n/a
6	BHLHE40	chr6:119255711-119256619	K562	blood:	n/a	n/a
7	BRCA1	chr6:119256054-119256142	GM12878	blood:	n/a	n/a
8	BRCA1	chr6:119255930-119256141	H1-hESC	embryonic stem cell:	n/a	n/a
9	CBX3	chr6:119257336-119257795	K562	blood:	n/a	n/a
10	CBX3	chr6:119255605-119256632	K562	blood:	n/a	n/a
11	CBX3	chr6:119257135-119257978	K562	blood:	n/a	n/a
12	CCNT2	chr6:119255564-119256544	K562	blood:	n/a	n/a
13	CEBPB	chr6:119254904-119254907	H1-hESC	embryonic stem cell:	n/a	n/a
14	CEBPB	chr6:119254752-119255061	Hela-S3	cervix:	n/a	chr6:119255048-119255061
15	CEBPB	chr6:119254797-119255085	HepG2	liver:	n/a	chr6:119255048-119255061
16	CEBPB	chr6:119255994-119256184	HepG2	liver:	n/a	n/a
17	CEBPB	chr6:119254836-119255047	A549	lung:	n/a	n/a
18	CEBPB	chr6:119255911-119256551	Hela-S3	cervix:	n/a	n/a
19	CEBPD	chr6:119255608-119256631	K562	blood:	n/a	n/a
20	CEBPD	chr6:119255588-119256470	HepG2	liver:	n/a	n/a
21	CHD1	chr6:119255863-119256021	H1-hESC	embryonic stem cell:	n/a	n/a
22	CHD1	chr6:119255821-119256107	GM12878	blood:	n/a	n/a
23	CHD1	chr6:119256534-119256568	H1-hESC	embryonic stem cell:	n/a	n/a
24	CHD2	chr6:119255757-119256202	K562	blood:	n/a	n/a
25	CHD2	chr6:119255663-119256583	Hela-S3	cervix:	n/a	chr6:119256389-119256399
26	CHD2	chr6:119256364-119256559	H1-hESC	embryonic stem cell:	n/a	chr6:119256389-119256399
27	CHD2	chr6:119255503-119256138	H1-hESC	embryonic stem cell:	n/a	n/a
28	CHD2	chr6:119255778-119256487	HepG2	liver:	n/a	chr6:119256389-119256399
29	CHD2	chr6:119255512-119256455	GM12878	blood:	n/a	chr6:119256389-119256399
30	CREB1	chr6:119255995-119256467	A549	lung:	n/a	n/a
31	CREB1	chr6:119255445-119256645	HepG2	liver:	n/a	n/a
32	CREB1	chr6:119255500-119256594	K562	blood:	n/a	n/a
33	CTCF	chr6:119251840-119251990	AG04450	lung:	n/a	n/a
34	CTCF	chr6:119252000-119252150	AoAF	blood vessel:	n/a	n/a
35	CTCF	chr6:119251900-119252050	AG10803	skin:	n/a	n/a
36	CTCF	chr6:119251880-119252030	HFF-Myc	foreskin:	n/a	n/a
37	CTCF	chr6:119251980-119252130	HPAF	blood vessel:	n/a	n/a
38	CTCF	chr6:119251940-119252090	HCT-116	colon:	n/a	n/a
39	CTCF	chr6:119251940-119252090	RPTEC	kidney:	n/a	n/a
40	CTCF	chr6:119251960-119252110	HBMEC	blood vessel:	n/a	n/a
41	CTCF	chr6:119251880-119252030	HCM	heart:	n/a	n/a
42	CTCF	chr6:119256172-119256416	Spleen_OC	spleen:	n/a	n/a
43	CTCF	chr6:119251980-119252130	RPTEC	kidney:	n/a	n/a
44	CTCF	chr6:119251880-119252030	HMEC	breast:	n/a	n/a
45	CTCF	chr6:119251960-119252110	HPAF	blood vessel:	n/a	n/a
46	CTCF	chr6:119256120-119256270	GM12871	blood:	n/a	n/a
47	CTCF	chr6:119255949-119256124	K562	blood:	n/a	n/a
48	CTCF	chr6:119251980-119252130	HCPEpiC	choroid plexus:	n/a	n/a
49	CTCF	chr6:119251960-119252110	HCPEpiC	choroid plexus:	n/a	n/a
50	CTCF	chr6:119252013-119252076	HepG2	liver:	n/a	n/a

(count:551 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:119255801-119255851	HRE	kidney:	n/a
2	chr6:119256092-119256142	Caco-2	colon:	n/a
3	chr6:119255801-119255851	HRE	kidney:	n/a
4	chr6:119256092-119256142	Caco-2	colon:	n/a
5	chr6:119256453-119256503	HepG2	liver:	n/a
6	chr6:119256162-119256212	GM12878	blood:	n/a
7	chr6:119256466-119256516	A549	lung:	n/a
8	chr6:119256284-119256334	NHDF-neo	bronchial:	n/a
9	chr6:119255801-119255851	Jurkat	blood:	n/a
10	chr6:119255874-119255924	AG09319	gingival:	n/a
11	chr6:119255801-119255851	HCT-116	colon:	n/a
12	chr6:119255801-119255851	AG04449	skin:	fetal
13	chr6:119256453-119256503	PFSK-1	brain:	n/a
14	chr6:119256092-119256142	IMR90	lung:	fetal
15	chr6:119256162-119256212	AG04449	skin:	fetal
16	chr6:119255801-119255851	HIPEpiC	eye:	n/a
17	chr6:119255801-119255851	HUVEC	blood vessel:	n/a
18	chr6:119252835-119252885	HRPEpiC	eye:	n/a
19	chr6:119256162-119256212	HRE	kidney:	n/a
20	chr6:119256466-119256516	GM12892	blood:	n/a
21	chr6:119256162-119256212	RPTEC	kidney:	n/a
22	chr6:119255801-119255851	PrEC	prostate:	n/a
23	chr6:119256162-119256212	Caco-2	colon:	n/a
24	chr6:119256284-119256334	HCT-116	colon:	n/a
25	chr6:119252835-119252885	AG09319	gingival:	n/a
26	chr6:119255812-119255862	U87	brain:	n/a
27	chr6:119256453-119256503	NHBE	bronchial:	n/a
28	chr6:119252835-119252885	BE2_C	brain:	n/a
29	chr6:119256453-119256503	IMR90	lung:	fetal
30	chr6:119252835-119252885	HMEC	breast:	n/a
31	chr6:119255801-119255851	ovcar-3	ovarian:	n/a
32	chr6:119255874-119255924	BJ	skin:	n/a
33	chr6:119252835-119252885	AG04449	skin:	fetal
34	chr6:119256284-119256334	GM12878	blood:	n/a
35	chr6:119256162-119256212	CMK	blood:	n/a
36	chr6:119252835-119252885	LNCaP	prostate:	n/a
37	chr6:119256092-119256142	AG09309	skin:	n/a
38	chr6:119256162-119256212	Hela-S3	cervix:	n/a
39	chr6:119256092-119256142	RPTEC	kidney:	n/a
40	chr6:119256284-119256334	HCPEpiC	choroid plexus:	n/a
41	chr6:119256092-119256142	SK-N-SH_RA	brain:	n/a
42	chr6:119256162-119256212	HIPEpiC	eye:	n/a
43	chr6:119256453-119256503	GM12892	blood:	n/a
44	chr6:119255812-119255862	AG09309	skin:	n/a
45	chr6:119255874-119255924	HRE	kidney:	n/a
46	chr6:119256466-119256516	GM19239	blood:	n/a
47	chr6:119255874-119255924	CMK	blood:	n/a
48	chr6:119256466-119256516	HNPCEpiC	eye:	n/a
49	chr6:119255812-119255862	PFSK-1	brain:	n/a
50	chr6:119255874-119255924	AoSMC	blood vessel:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr6:119257082..119259694-chr6:119259960..119261722,2	K562	blood:
2	chr6:119253238..119258280-chr6:119398045..119402661,8	K562	blood:
3	chr6:119256349..119258481-chr6:119264695..119266812,2	K562	blood:
4	chr6:119256205..119257932-chr6:119293855..119296677,2	K562	blood:
5	chr3:155571664..155572210-chr6:119255210..119256056,2	Hela-S3	cervix:
6	chr15:90708735..90709594-chr6:119255785..119256642,2	HCT-116	colon:
7	chr6:119213036..119217484-chr6:119254311..119257675,9	MCF-7	breast:
8	chr6:119255727..119258203-chr6:119400226..119402388,2	K562	blood:
9	chr6:119251278..119254603-chr6:119254723..119256647,5	MCF-7	breast:
10	chr1:28907889..28908475-chr6:119255713..119256233,2	Hela-S3	cervix:
11	chr6:119230403..119232175-chr6:119251881..119254660,2	K562	blood:
12	chr6:119250858..119252631-chr6:119254027..119256960,4	MCF-7	breast:
13	chr6:119256106..119257947-chr6:119468580..119471034,2	K562	blood:
14	chr6:119246982..119248806-chr6:119249429..119252283,2	K562	blood:
15	chr6:119216722..119218492-chr6:119251658..119253168,2	K562	blood:
16	chr6:119213694..119219544-chr6:119251621..119258172,21	K562	blood:
17	chr6:119257082..119259694-chr6:119259960..119261722,2	K562	blood:
18	chr6:119235128..119240237-chr6:119246100..119252076,6	K562	blood:
19	chr6:119255269..119257410-chr6:119258085..119262508,5	MCF-7	breast:
20	chr6:119230305..119231903-chr6:119251881..119253560,2	K562	blood:
21	chr6:119235730..119238725-chr6:119250576..119253329,2	K562	blood:
22	chr5:56205869..56206380-chr6:119255621..119256581,2	Hela-S3	cervix:
23	chr6:119252974..119255408-chr6:119376994..119379902,2	K562	blood:
24	chr4:79472622..79473237-chr6:119256049..119256758,2	HCT-116	colon:
25	chr6:119214552..119219906-chr6:119253918..119257622,8	MCF-7	breast:
26	chr6:119253156..119256806-chr6:119394976..119399977,7	K562	blood:
27	chr6:119213105..119220728-chr6:119253299..119257962,22	K562	blood:
28	chr1:149223435..149224292-chr6:119255876..119256729,2	HCT-116	colon:
29	chr6:119225449..119227305-chr6:119252060..119254076,2	K562	blood:
30	chr6:119256460..119259122-chr6:119259921..119263121,4	K562	blood:
31	chr6:119148024..119150788-chr6:119254470..119256543,2	MCF-7	breast:
32	chr10:74927354..74928318-chr6:119255751..119256642,2	NB4	blood:
33	chr6:119220702..119224795-chr6:119249246..119252141,5	K562	blood:
34	chr6:119242613..119249110-chr6:119251513..119257145,6	MCF-7	breast:
35	chr6:119256460..119259122-chr6:119259921..119263121,4	K562	blood:

No data

Variant related genes	Relation type
ENSG00000253194	TF binding region
MCM9	TF binding region
ENSG00000253194	CpG island
MCM9	CpG island
ENSG00000111877	chromatin interactions
ENSG00000122882	chromatin interactions
ENSG00000138772	chromatin interactions
ENSG00000206737	chromatin interactions
ENSG00000253194	chromatin interactions
ENSG00000197989	chromatin interactions
ENSG00000169359	chromatin interactions
ENSG00000240470	chromatin interactions
ENSG00000138286	chromatin interactions
ENSG00000111879	chromatin interactions
ENSG00000222649	chromatin interactions
ENSG00000111875	chromatin interactions
ENSG00000155542	chromatin interactions

Extended variants
information (count: 344 )
Associated
traits (count: 113 )

Variant overlapped rSNPs/rCNVs (count:344 , 50 per page) page: 1 2 3 4 5 6 7

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1022707	chr6:119251971-119251972	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs570964843	chr6:119251976-119251977	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs1022706	chr6:119252006-119252007	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
4	rs6918844	chr6:119252028-119252029	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
5	rs115854365	chr6:119252040-119252041	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs540678807	chr6:119252056-119252057	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs112684721	chr6:119252106-119252107	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs6918569	chr6:119252111-119252112	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
9	rs116531433	chr6:119252238-119252239	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs569243580	chr6:119252271-119252272	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs531872959	chr6:119252301-119252302	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs150390174	chr6:119252328-119252329	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs570067315	chr6:119252335-119252336	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs116103059	chr6:119252365-119252366	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs6919100	chr6:119252400-119252401	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
16	rs549156457	chr6:119252410-119252411	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs368920933	chr6:119252515-119252516	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs77276008	chr6:119252564-119252565	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs369432216	chr6:119252570-119252571	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs372076068	chr6:119252593-119252594	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs376739285	chr6:119252646-119252647	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs150149318	chr6:119252663-119252664	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs369648810	chr6:119252664-119252665	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs531682044	chr6:119252668-119252669	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs73521381	chr6:119252676-119252677	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs116063933	chr6:119252705-119252706	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs141489965	chr6:119252711-119252712	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs146928835	chr6:119252716-119252717	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs55738219	chr6:119252721-119252722	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs549795259	chr6:119252726-119252727	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs571254679	chr6:119252737-119252738	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs374030416	chr6:119252750-119252751	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs188323243	chr6:119252767-119252768	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs377754318	chr6:119252795-119252796	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs370026912	chr6:119252827-119252828	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs114642748	chr6:119252836-119252837	Weak transcription Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs370073393	chr6:119252839-119252840	Weak transcription Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs149471755	chr6:119252874-119252875	Weak transcription Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs115231232	chr6:119252883-119252884	Weak transcription Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs374755975	chr6:119252896-119252897	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs202154584	chr6:119252905-119252906	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs138548191	chr6:119252931-119252932	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs374206337	chr6:119252933-119252934	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs531928658	chr6:119252967-119252968	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs551649371	chr6:119252976-119252977	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
46	rs563773047	chr6:119252993-119252994	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
47	rs144065765	chr6:119253006-119253007	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
48	rs546250102	chr6:119253095-119253096	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
49	rs368183247	chr6:119253116-119253117	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
50	rs9401100	chr6:119253143-119253144	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:113)

Disease	PMID	Source
Uveal melanoma	21693616	CNVD
Glioblastoma multiforme	21080181	CNVD
Biliary cancer	19435499	CNVD
Medulloblastoma	21979893	CNVD
Malaria	21533027	CNVD
T-cell prolymphocytic leukemia	19278963	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
Autism	22495311	CNVD
Gastric cancer	17908304	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
Acute lymphoblastic leukemia	22237106	CNVD
Neuroblastoma	18923191	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Melanoma	18172304	CNVD
Cancer	21637783	CNVD
Colorectal cancer	16272173	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
T-cell lymphomas	19863542	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Follicular lymphoma	19010834	CNVD
Non-small cell lung cancer	21044232	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	16608533	CNVD
Non-small cell lung cancer	21385341	CNVD
Prostate cancer	16705090	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Ependymoma	16718352	CNVD
High-proliferative meningiomas	17937814	CNVD
Intracranial tumor	16823260	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	16272173	CNVD
Prostate cancer	18632612	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Urothelial carcinoma	18382360	CNVD
Ovarian neoplasms	16753589	CNVD
Hepatocellular carcinoma	16750200	CNVD
Wilms tumour	21544195	CNVD
Prostate cancer	19242612	CNVD
Glioma	21046410	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Zellweger syndrome	21572526	CNVD
Follicular lymphoma	20505157	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Malignant melanoma	18718029	CNVD
Lung adenocarcinoma	21935476	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21858162	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	17603634	CNVD
Chondromyxoid Fibroma	20696777	CNVD
Cancer	21183584	CNVD
Developmental delay	19490664	CNVD
Non-muscle invasive bladder neoplasm	19445696	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Burkitt''s lymphoma	18698080	CNVD
Ovarian cancer	21720365	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Breast cancer	21785460	CNVD
Prostate cancer	16461572	CNVD
Neurocytoma	17123091	CNVD
Cancer	20164920	CNVD
Breast cancer	21364760	CNVD
Chordoma	21602918	CNVD
Kartagener syndrome	16639409	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	17133270	CNVD
Follicular lymphoma	18703704	CNVD
Mental retardation	17621639	CNVD
Hypoplastic	20877625	CNVD
Hypotonia	20877625	CNVD
Mental retardation	20877625	CNVD
Microcephaly	20877625	CNVD
brachycephaly	20877625	CNVD
epicanthic folds	20877625	CNVD
micrognathia	20877625	CNVD
Neurodevelopmental disorder	22521361	CNVD
small cell lung cancer	20016488	CNVD
Metastatic melanoma	18483359	CNVD
Adenoid cystic carcinoma	18698036	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Breast cancer	18698023	CNVD
Mental retardation	18854857	CNVD
Leukemia	18688285	CNVD
Myelofibrosis	22110671	CNVD
Intellectual disability	22045946	CNVD
Liver carcinoma	19366792	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:661 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:119219200-119254000	Strong transcription	Monocytes-CD14+_RO01746	blood
2	chr6:119219200-119254400	Strong transcription	Placenta	Placenta
3	chr6:119219600-119253000	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
4	chr6:119219600-119253800	Strong transcription	Primary hematopoietic stem cells short term culture	blood
5	chr6:119221200-119255800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr6:119222000-119254000	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
7	chr6:119222000-119254400	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr6:119222000-119255200	Weak transcription	Fetal Heart	heart
9	chr6:119222200-119253400	Strong transcription	Fetal Intestine Large	intestine
10	chr6:119222600-119253800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
11	chr6:119222600-119253800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
12	chr6:119224000-119254000	Strong transcription	HUES64 Cell Line	embryonic stem cell
13	chr6:119224200-119252800	Strong transcription	Primary neutrophils fromperipheralblood	blood
14	chr6:119224600-119254000	Strong transcription	Breast Myoepithelial Primary Cells	Breast
15	chr6:119224800-119254800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
16	chr6:119226000-119255200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
17	chr6:119227000-119254800	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
18	chr6:119227400-119252000	Weak transcription	Small Intestine	intestine
19	chr6:119227400-119253800	Strong transcription	Primary T helper cells fromperipheralblood	blood
20	chr6:119227800-119254800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
21	chr6:119228000-119253000	Strong transcription	Primary T helper cells PMA-I stimulated	--
22	chr6:119228200-119253400	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
23	chr6:119235600-119255200	Weak transcription	Fetal Brain Male	brain
24	chr6:119235600-119255400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
25	chr6:119236000-119253400	Strong transcription	Liver	Liver
26	chr6:119236600-119254000	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
27	chr6:119236600-119255200	Weak transcription	Right Ventricle	heart
28	chr6:119237000-119255200	Weak transcription	Brain Germinal Matrix	brain
29	chr6:119237000-119255200	Weak transcription	Gastric	stomach
30	chr6:119237200-119255200	Weak transcription	Brain Angular Gyrus	brain
31	chr6:119239600-119253800	Strong transcription	Primary B cells from cord blood	blood
32	chr6:119239800-119255200	Weak transcription	NHLF	lung
33	chr6:119240000-119255200	Weak transcription	Fetal Brain Female	brain
34	chr6:119240400-119252800	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
35	chr6:119241000-119254800	Weak transcription	Pancreatic Islets	Pancreatic Islet
36	chr6:119242600-119255200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
37	chr6:119242600-119255200	Weak transcription	Colonic Mucosa	Colon
38	chr6:119242800-119252600	Weak transcription	NHDF-Ad	bronchial
39	chr6:119242800-119255800	Weak transcription	Spleen	Spleen
40	chr6:119243000-119255200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
41	chr6:119243400-119253600	Weak transcription	Stomach Mucosa	stomach
42	chr6:119243400-119255200	Weak transcription	H9 Cell Line	embryonic stem cell
43	chr6:119243600-119254000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
44	chr6:119243800-119254800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
45	chr6:119243800-119254800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
46	chr6:119244000-119252000	Weak transcription	Brain Inferior Temporal Lobe	brain
47	chr6:119244000-119255200	Weak transcription	Brain Cingulate Gyrus	brain
48	chr6:119244000-119255400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
49	chr6:119244600-119255200	Weak transcription	Aorta	Aorta
50	chr6:119244800-119254800	Weak transcription	Rectal Smooth Muscle	rectum

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