Variant report

Variant	nsv997261
Chromosome Location	chr3:47054766-47133680
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:666)
CpG islands
(count:122)
Chromatin interactive
region (count:43)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:1)

(count:666 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr3:47106469-47106658	K562	blood:	n/a	n/a
2	ARID3A	chr3:47058567-47059013	K562	blood:	n/a	n/a
3	ARID3A	chr3:47107096-47107637	HepG2	liver:	n/a	n/a
4	ATF1	chr3:47067066-47067074	K562	blood:	n/a	n/a
5	ATF1	chr3:47066643-47066842	K562	blood:	n/a	n/a
6	ATF1	chr3:47058405-47059340	K562	blood:	n/a	n/a
7	ATF2	chr3:47098859-47099214	GM12878	blood:	n/a	n/a
8	ATF2	chr3:47098768-47099254	GM12878	blood:	n/a	n/a
9	BACH1	chr3:47058771-47058869	K562	blood:	n/a	n/a
10	BATF	chr3:47096004-47096213	GM12878	blood:	n/a	chr3:47096184-47096193
11	BATF	chr3:47066489-47066773	GM12878	blood:	n/a	chr3:47066583-47066594
12	BATF	chr3:47098727-47099201	GM12878	blood:	n/a	n/a
13	BATF	chr3:47060655-47061006	GM12878	blood:	n/a	chr3:47060841-47060852
14	BATF	chr3:47124036-47124433	GM12878	blood:	n/a	n/a
15	BATF	chr3:47060691-47061028	GM12878	blood:	n/a	chr3:47060841-47060852
16	BATF	chr3:47124091-47124363	GM12878	blood:	n/a	n/a
17	BCL3	chr3:47115268-47115582	GM12878	blood:	n/a	n/a
18	BCL3	chr3:47098830-47099222	GM12878	blood:	n/a	n/a
19	BHLHE40	chr3:47059601-47059747	K562	blood:	n/a	n/a
20	BHLHE40	chr3:47079453-47079711	GM12878	blood:	n/a	n/a
21	BHLHE40	chr3:47058450-47058931	K562	blood:	n/a	n/a
22	BHLHE40	chr3:47084005-47084234	K562	blood:	n/a	n/a
23	CBX3	chr3:47058208-47059036	K562	blood:	n/a	n/a
24	CCNT2	chr3:47058590-47058955	K562	blood:	n/a	n/a
25	CCNT2	chr3:47057703-47058125	K562	blood:	n/a	n/a
26	CEBPB	chr3:47092191-47092322	K562	blood:	n/a	n/a
27	CEBPB	chr3:47099603-47099881	A549	lung:	n/a	chr3:47099748-47099759
28	CEBPB	chr3:47059095-47059318	HepG2	liver:	n/a	n/a
29	CEBPB	chr3:47081975-47082280	IMR90	lung:	n/a	chr3:47082120-47082131
30	CEBPB	chr3:47128361-47128554	H1-hESC	embryonic stem cell:	n/a	chr3:47128481-47128492
31	CEBPB	chr3:47128359-47128629	K562	blood:	n/a	chr3:47128481-47128492
32	CEBPB	chr3:47123964-47124541	IMR90	lung:	n/a	n/a
33	CEBPB	chr3:47088626-47088856	K562	blood:	n/a	chr3:47088714-47088725
34	CEBPB	chr3:47133607-47133954	HepG2	liver:	n/a	chr3:47133782-47133791 chr3:47133780-47133793 chr3:47133782-47133791 chr3:47133782-47133791 chr3:47133639-47133650 chr3:47133780-47133793 chr3:47133781-47133792 chr3:47133782-47133791 chr3:47133780-47133791
35	CEBPB	chr3:47058703-47058707	K562	blood:	n/a	n/a
36	CEBPB	chr3:47081966-47082212	K562	blood:	n/a	chr3:47082120-47082131
37	CEBPB	chr3:47106017-47106262	HepG2	liver:	n/a	chr3:47106168-47106179
38	CEBPB	chr3:47107185-47107570	HepG2	liver:	n/a	n/a
39	CEBPB	chr3:47099578-47099862	Hela-S3	cervix:	n/a	chr3:47099748-47099759
40	CEBPB	chr3:47058421-47058898	IMR90	lung:	n/a	n/a
41	CEBPB	chr3:47128322-47128640	IMR90	lung:	n/a	chr3:47128481-47128492
42	CEBPB	chr3:47133607-47133967	IMR90	lung:	n/a	chr3:47133782-47133791 chr3:47133780-47133793 chr3:47133782-47133791 chr3:47133782-47133791 chr3:47133639-47133650 chr3:47133780-47133793 chr3:47133781-47133792 chr3:47133782-47133791 chr3:47133780-47133791
43	CEBPB	chr3:47104278-47104431	HepG2	liver:	n/a	chr3:47104383-47104394
44	CEBPB	chr3:47133624-47133897	A549	lung:	n/a	chr3:47133782-47133791 chr3:47133780-47133793 chr3:47133782-47133791 chr3:47133782-47133791 chr3:47133639-47133650 chr3:47133780-47133793 chr3:47133781-47133792 chr3:47133782-47133791 chr3:47133780-47133791
45	CEBPB	chr3:47128336-47128584	HepG2	liver:	n/a	chr3:47128481-47128492
46	CEBPB	chr3:47133659-47133865	H1-hESC	embryonic stem cell:	n/a	chr3:47133782-47133791 chr3:47133780-47133793 chr3:47133782-47133791 chr3:47133782-47133791 chr3:47133780-47133793 chr3:47133781-47133792 chr3:47133782-47133791 chr3:47133780-47133791
47	CEBPB	chr3:47059745-47060093	HepG2	liver:	n/a	n/a
48	CEBPB	chr3:47099588-47099878	HepG2	liver:	n/a	chr3:47099748-47099759
49	CEBPB	chr3:47128364-47128687	ECC-1	luminal epithelium:	n/a	chr3:47128481-47128492
50	CEBPB	chr3:47089171-47089443	K562	blood:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:47066821-47066871	AG09309	skin:	n/a
2	chr3:47066821-47066871	SAEC	small airway:	n/a
3	chr3:47058276-47058326	Hepatocyte	liver:	n/a
4	chr3:47066821-47066871	GM06990	blood:	n/a
5	chr3:47058276-47058326	HAEpiC	amniotic membrane:	n/a
6	chr3:47066821-47066871	HCT-116	colon:	n/a
7	chr3:47066821-47066871	ProgFib	skin:	n/a
8	chr3:47058276-47058326	GM19239	blood:	n/a
9	chr3:47058276-47058326	PANC-1	pancreas:	n/a
10	chr3:47058276-47058326	AG04449	skin:	fetal
11	chr3:47058276-47058326	GM06990	blood:	n/a
12	chr3:47066821-47066871	ECC-1	luminal epithelium:	n/a
13	chr3:47058276-47058326	HRE	kidney:	n/a
14	chr3:47058276-47058326	PrEC	prostate:	n/a
15	chr3:47058276-47058326	BJ	skin:	n/a
16	chr3:47066821-47066871	BJ	skin:	n/a
17	chr3:47066821-47066871	HAEpiC	amniotic membrane:	n/a
18	chr3:47066821-47066871	HCM	heart:	n/a
19	chr3:47066821-47066871	AG10803	skin:	n/a
20	chr3:47066821-47066871	HRE	kidney:	n/a
21	chr3:47066821-47066871	GM12891	blood:	n/a
22	chr3:47066821-47066871	MCF-7	breast:	n/a
23	chr3:47058276-47058326	HIPEpiC	eye:	n/a
24	chr3:47058276-47058326	ovcar-3	ovarian:	n/a
25	chr3:47066821-47066871	Hepatocyte	liver:	n/a
26	chr3:47058276-47058326	GM12891	blood:	n/a
27	chr3:47058276-47058326	HEK293	kidney:	embryo
28	chr3:47058276-47058326	Hela-S3	cervix:	n/a
29	chr3:47058276-47058326	SAEC	small airway:	n/a
30	chr3:47066821-47066871	BE2_C	brain:	n/a
31	chr3:47058276-47058326	SK-N-MC	brain:	n/a
32	chr3:47058276-47058326	AG09309	skin:	n/a
33	chr3:47066821-47066871	H1-hESC	embryonic stem cell:	embryo
34	chr3:47066821-47066871	GM19239	blood:	n/a
35	chr3:47058276-47058326	SK-N-SH	brain:	n/a
36	chr3:47058276-47058326	RPTEC	kidney:	n/a
37	chr3:47058276-47058326	SK-N-SH_RA	brain:	n/a
38	chr3:47058276-47058326	NHDF-neo	bronchial:	n/a
39	chr3:47066821-47066871	PANC-1	pancreas:	n/a
40	chr3:47066821-47066871	AG09319	gingival:	n/a
41	chr3:47066821-47066871	AoSMC	blood vessel:	n/a
42	chr3:47058276-47058326	HNPCEpiC	eye:	n/a
43	chr3:47066821-47066871	NB4	blood:	n/a
44	chr3:47066821-47066871	HL-60	blood:	n/a
45	chr3:47066821-47066871	HNPCEpiC	eye:	n/a
46	chr3:47058276-47058326	MCF10A-Er-Src	breast:	n/a
47	chr3:47066821-47066871	RPTEC	kidney:	n/a
48	chr3:47058276-47058326	NT2-D1	testis:	n/a
49	chr3:47058276-47058326	T-47D	breast:	n/a
50	chr3:47066821-47066871	SK-N-SH_RA	brain:	n/a

(count:43 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr3:47098199..47100265-chr3:47118377..47121357,2	MCF-7	breast:
2	chr3:47117444..47119975-chr3:47141387..47143617,2	K562	blood:
3	chr3:47082604..47084164-chr3:47087207..47088724,2	K562	blood:
4	chr3:47108569..47110745-chr3:47111424..47113909,2	MCF-7	breast:
5	chr3:47115603..47117354-chr3:47121967..47124210,2	K562	blood:
6	chr3:47122254..47124275-chr3:47192922..47194900,2	K562	blood:
7	chr3:47098565..47100526-chr3:47102851..47105767,2	K562	blood:
8	chr3:47097362..47099843-chr3:47113301..47116271,2	K562	blood:
9	chr3:47122352..47125407-chr3:47126462..47130249,3	K562	blood:
10	chr3:47081998..47084579-chr3:47088555..47090930,2	K562	blood:
11	chr3:47056274..47058537-chr3:47060198..47062486,2	K562	blood:
12	chr3:47098199..47100265-chr3:47118377..47121357,2	MCF-7	breast:
13	chr3:47068198..47069925-chr3:47079015..47080516,2	K562	blood:
14	chr3:47099343..47101567-chr3:47110019..47111796,2	K562	blood:
15	chr3:47068198..47069925-chr3:47079015..47080516,2	K562	blood:
16	chr3:47072469..47075207-chr3:47077387..47079210,2	K562	blood:
17	chr3:47069157..47071799-chr3:47073550..47075911,2	K562	blood:
18	chr3:47066773..47068763-chr3:47068912..47071428,2	K562	blood:
19	chr3:47114506..47116285-chr3:47366485..47368143,2	K562	blood:
20	chr3:47072469..47075207-chr3:47077387..47079210,2	K562	blood:
21	chr3:47113958..47116821-chr3:47117778..47119607,2	K562	blood:
22	chr3:47108569..47110745-chr3:47111424..47113909,2	MCF-7	breast:
23	chr3:47125477..47129323-chr3:47137612..47139651,3	K562	blood:
24	chr3:47099343..47101567-chr3:47110019..47111796,2	K562	blood:
25	chr3:47104888..47106552-chr3:47109440..47111532,2	K562	blood:
26	chr3:47074366..47076191-chr3:47079494..47081958,2	K562	blood:
27	chr3:47132552..47135430-chr4:99181740..99183260,2	MCF-7	breast:
28	chr3:47069157..47071799-chr3:47073550..47075911,2	K562	blood:
29	chr3:47113958..47116821-chr3:47117778..47119607,2	K562	blood:
30	chr3:47115603..47117354-chr3:47121967..47124210,2	K562	blood:
31	chr3:46985961..46989571-chr3:47058662..47060411,3	K562	blood:
32	chr3:47047312..47050228-chr3:47050509..47055807,4	MCF-7	breast:
33	chr3:47097362..47099843-chr3:47113301..47116271,2	K562	blood:
34	chr3:47081998..47084579-chr3:47088555..47090930,2	K562	blood:
35	chr3:47051592..47055905-chr3:47059567..47061970,4	K562	blood:
36	chr3:47110983..47113551-chr3:47421604..47424088,2	MCF-7	breast:
37	chr3:47056274..47058537-chr3:47060198..47062486,2	K562	blood:
38	chr3:47121965..47124709-chr3:47429013..47430772,2	K562	blood:
39	chr3:47074366..47076191-chr3:47079494..47081958,2	K562	blood:
40	chr3:47066773..47068763-chr3:47068912..47071428,2	K562	blood:
41	chr3:47118002..47122103-chr3:47123133..47127114,5	K562	blood:
42	chr3:47104888..47106552-chr3:47109440..47111532,2	K562	blood:
43	chr3:47098565..47100526-chr3:47102851..47105767,2	K562	blood:

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	SETD2	hsa-miR-106b-5p	chr3:47057981-47058000

Variant related genes	Relation type
ENSG00000251938	TF binding region
SETD2	TF binding region
ENSG00000251938	CpG island
SETD2	CpG island
ENSG00000160796	chromatin interactions
ENSG00000076201	chromatin interactions
ENSG00000236409	chromatin interactions
ENSG00000260236	chromatin interactions
ENSG00000181555	chromatin interactions
ENSG00000214559	chromatin interactions
ENSG00000251938	chromatin interactions
ENSG00000138698	chromatin interactions

Extended variants
information (count: 2635 )
Associated
traits (count: 100 )

Variant overlapped rSNPs/rCNVs (count:2635 , 50 per page) page: 1 2 3 4 5 6 7 ... 53

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1013448	chr3:47054766-47054767	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs530925901	chr3:47054772-47054773	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs552644563	chr3:47054786-47054787	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs570818936	chr3:47054860-47054861	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs2278963	chr3:47054869-47054870	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
6	rs547250207	chr3:47054899-47054900	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs573540936	chr3:47055001-47055002	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs182208225	chr3:47055026-47055027	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs35600346	chr3:47055027-47055028	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs541990228	chr3:47055096-47055097	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs553926311	chr3:47055128-47055129	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs150815844	chr3:47055177-47055178	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs36204073	chr3:47055187-47055188	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs543821098	chr3:47055197-47055198	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs569311607	chr3:47055234-47055235	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs546465273	chr3:47055280-47055281	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs564368940	chr3:47055301-47055302	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs187633579	chr3:47055328-47055329	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs531683238	chr3:47055333-47055334	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs543570027	chr3:47055340-47055341	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs192558863	chr3:47055418-47055419	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs576835547	chr3:47055469-47055470	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs372202401	chr3:47055473-47055474	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs184278169	chr3:47055485-47055486	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs553637739	chr3:47055538-47055539	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs575076934	chr3:47055562-47055563	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs188487535	chr3:47055630-47055631	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs150056180	chr3:47055656-47055657	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs530945366	chr3:47055662-47055663	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs545845625	chr3:47055680-47055681	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs543369374	chr3:47055683-47055684	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs145426085	chr3:47055704-47055705	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs71328911	chr3:47055711-47055712	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs9847829	chr3:47055755-47055756	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs184587503	chr3:47055798-47055799	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs189857792	chr3:47055825-47055826	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs75164761	chr3:47055828-47055829	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs11922323	chr3:47055860-47055861	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs548087137	chr3:47055871-47055872	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs180765109	chr3:47055897-47055898	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs183857038	chr3:47055911-47055912	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs149189829	chr3:47055954-47055955	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs115224465	chr3:47055972-47055973	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs143851020	chr3:47055996-47055997	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs534460451	chr3:47055997-47055998	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs78415191	chr3:47056034-47056035	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs368674568	chr3:47056134-47056135	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs575090956	chr3:47056157-47056158	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs189410698	chr3:47056167-47056168	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs182015940	chr3:47056172-47056173	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:100)

Disease	PMID	Source
Lynch syndrome	18415027	CNVD
Renal cell carcinoma	18592004	CNVD
Acute myeloid leukemia	20729466	CNVD
Urothelial carcinoma	18382360	CNVD
Melanoma	18172304	CNVD
Cervical cancer	21062161	CNVD
Hirschsprung''s Disease	21712996	CNVD
Glioblastoma multiforme	21080181	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Insulin resistance	16721378	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	21484798	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Oral cancer	19627613	CNVD
Renal cell carcinoma	19461508	CNVD
Epithelial cancer	22065749	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Acute myeloid leukemia	16864856	CNVD
Liposarcoma	21253554	CNVD
Basal cell lymphoma	21115979	CNVD
Endometrial cancer	22040021	CNVD
Pancreatic endocrine tumor	20981439	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	17387387	CNVD
Oral cancer	21386901	CNVD
Cutaneous squamous cell carcinomas	19131950	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Retinoblastoma	21504564	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Renal cell carcinoma	21668985	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Thoracic aortic aneurysm	21092924	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	17603634	CNVD
Esophageal cancer	20955586	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Breast cancer	17133270	CNVD
Uveal melanoma	20484589	CNVD
Autism	22495311	CNVD
Melanoma	20688739	CNVD
Acute myeloid leukemia	21251322	CNVD
Hepatocellular carcinoma	16750200	CNVD
Cancer	21183584	CNVD
Kartagener syndrome	16639409	CNVD
Biliary cancer	19435499	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Bipolar disorder	20877625	CNVD
Bipolar disorder	21956041	CNVD
Bipolar disorder	22241247	CNVD
Biliary cancer	18923514	CNVD
Breast cancer	21509527	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	16397240	CNVD
Breast cancer	22032731	CNVD
Non-small cell lung cancer	20864512	CNVD
Colorectal cancer	16912164	CNVD
Non-small cell lung cancer	19010865	CNVD
Colorectal cancer	16272173	CNVD
Non-muscle invasive bladder neoplasm	19445696	CNVD
Acute myeloid leukemia	17268525	CNVD
Salivary gland tumor	18059337	CNVD
Gastric cancer	16891809	CNVD
Night blindness	17160897	CNVD
Cancer	17160897	CNVD
Breast cancer	20409316	CNVD
Lung cancer	17297452	CNVD
Multiple myeloma	16616336	CNVD
Effusion lymphoma	18079361	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Neuroblastoma	20406844	CNVD
Breast cancer	21785460	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	21045282	CNVD
Urothelial cell carcinoma	18451213	CNVD
Neuroblastoma	17327916	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Melanoma	17363583	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Adrenocortical carcinoma	18281524	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
Medullary thyroid carcinoma	18765511	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:2857 , 50 per page) page: 1 2 3 4 5 6 7 ... 58

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:47039800-47058000	Strong transcription	Primary neutrophils fromperipheralblood	blood
2	chr3:47043800-47057800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
3	chr3:47045000-47057600	Weak transcription	HepG2	liver
4	chr3:47048600-47055800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr3:47049000-47055000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
6	chr3:47049000-47055400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr3:47049800-47058200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
8	chr3:47050200-47058200	Weak transcription	Hela-S3	cervix
9	chr3:47050200-47059000	Weak transcription	A549	lung
10	chr3:47050200-47063800	Weak transcription	Stomach Mucosa	stomach
11	chr3:47050400-47057600	Weak transcription	K562	blood
12	chr3:47051200-47058400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
13	chr3:47051400-47055200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
14	chr3:47051400-47056800	Weak transcription	HMEC	breast
15	chr3:47051400-47056800	Weak transcription	NHEK	skin
16	chr3:47051400-47058200	Weak transcription	Pancreatic Islets	Pancreatic Islet
17	chr3:47051400-47064000	Weak transcription	Small Intestine	intestine
18	chr3:47051600-47055000	Weak transcription	Sigmoid Colon	Sigmoid Colon
19	chr3:47051600-47055200	Weak transcription	Liver	Liver
20	chr3:47051600-47055400	Weak transcription	Fetal Kidney	kidney
21	chr3:47051600-47055600	Weak transcription	Rectal Mucosa Donor 31	rectum
22	chr3:47051600-47057600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
23	chr3:47051600-47058200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
24	chr3:47051600-47058400	Strong transcription	Primary monocytes fromperipheralblood	blood
25	chr3:47051600-47058400	Strong transcription	Monocytes-CD14+_RO01746	blood
26	chr3:47051800-47054800	Weak transcription	Rectal Mucosa Donor 29	rectum
27	chr3:47051800-47055200	Weak transcription	Primary T helper cells fromperipheralblood	blood
28	chr3:47051800-47055200	Enhancers	Fetal Thymus	thymus
29	chr3:47051800-47055400	Weak transcription	Primary T cells from cord blood	blood
30	chr3:47051800-47055600	Weak transcription	Brain Angular Gyrus	brain
31	chr3:47051800-47056800	Weak transcription	Aorta	Aorta
32	chr3:47051800-47056800	Weak transcription	Ovary	ovary
33	chr3:47051800-47057000	Weak transcription	Primary T helper cells PMA-I stimulated	--
34	chr3:47051800-47060400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
35	chr3:47051800-47061600	Weak transcription	Right Atrium	heart
36	chr3:47051800-47062000	Weak transcription	Psoas Muscle	Psoas
37	chr3:47052000-47054800	Weak transcription	Brain Cingulate Gyrus	brain
38	chr3:47052000-47055000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
39	chr3:47052000-47055000	Weak transcription	Brain Hippocampus Middle	brain
40	chr3:47052000-47055200	Weak transcription	Primary T cells fromperipheralblood	blood
41	chr3:47052000-47055200	Weak transcription	Muscle Satellite Cultured Cells	--
42	chr3:47052000-47055200	Weak transcription	NH-A	brain
43	chr3:47052000-47055400	Weak transcription	GM12878-XiMat	blood
44	chr3:47052000-47055400	Weak transcription	NHLF	lung
45	chr3:47052000-47055600	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
46	chr3:47052000-47055600	Weak transcription	Brain Substantia Nigra	brain
47	chr3:47052000-47055800	Strong transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
48	chr3:47052000-47056400	Weak transcription	Cortex derived primary cultured neurospheres	brain
49	chr3:47052000-47056600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
50	chr3:47052000-47056800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain

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