Variant report

Variant	nsv518363
Chromosome Location	chr2:9777229-9788315
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:325)
CpG islands
(count:61)
Chromatin interactive
region (count:36)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:325 , 50 per page) page: 1 2 3 4 5 6 7

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:9782841-9783136	K562	blood:	n/a	n/a
2	ARID3A	chr2:9778752-9778986	K562	blood:	n/a	n/a
3	ARID3A	chr2:9777460-9777529	HepG2	liver:	n/a	n/a
4	ARID3A	chr2:9788302-9788324	HepG2	liver:	n/a	n/a
5	ATF3	chr2:9778698-9778919	K562	blood:	n/a	n/a
6	BACH1	chr2:9778912-9779031	K562	blood:	n/a	n/a
7	BATF	chr2:9781709-9782039	GM12878	blood:	n/a	n/a
8	BATF	chr2:9781424-9781656	GM12878	blood:	n/a	n/a
9	BATF	chr2:9777365-9777778	GM12878	blood:	n/a	chr2:9777537-9777547 chr2:9777536-9777547
10	BATF	chr2:9781700-9782092	GM12878	blood:	n/a	n/a
11	BHLHE40	chr2:9787987-9788389	HepG2	liver:	n/a	n/a
12	BHLHE40	chr2:9777509-9777817	GM12878	blood:	n/a	n/a
13	BHLHE40	chr2:9782832-9783198	K562	blood:	n/a	n/a
14	BHLHE40	chr2:9785550-9785862	K562	blood:	n/a	chr2:9785685-9785698 chr2:9785681-9785702 chr2:9785686-9785695 chr2:9785687-9785696 chr2:9785687-9785696
15	BHLHE40	chr2:9778575-9779051	K562	blood:	n/a	n/a
16	BHLHE40	chr2:9778643-9778972	HepG2	liver:	n/a	n/a
17	BHLHE40	chr2:9779917-9780465	K562	blood:	n/a	n/a
18	BHLHE40	chr2:9780055-9780511	HepG2	liver:	n/a	n/a
19	BHLHE40	chr2:9778655-9778966	A549	lung:	n/a	n/a
20	CBX3	chr2:9778593-9779038	K562	blood:	n/a	n/a
21	CBX3	chr2:9782781-9783205	K562	blood:	n/a	n/a
22	CCNT2	chr2:9782846-9783180	K562	blood:	n/a	n/a
23	CCNT2	chr2:9780102-9780360	K562	blood:	n/a	n/a
24	CCNT2	chr2:9778683-9778952	K562	blood:	n/a	n/a
25	CEBPB	chr2:9782377-9782378	A549	lung:	n/a	n/a
26	CEBPB	chr2:9780495-9780825	A549	lung:	n/a	chr2:9780664-9780675 chr2:9780664-9780677
27	CEBPB	chr2:9778803-9779007	K562	blood:	n/a	n/a
28	CEBPB	chr2:9780507-9780840	IMR90	lung:	n/a	chr2:9780664-9780675 chr2:9780664-9780677
29	CEBPB	chr2:9788075-9788276	HepG2	liver:	n/a	n/a
30	CEBPB	chr2:9780510-9780825	Hela-S3	cervix:	n/a	chr2:9780664-9780675 chr2:9780664-9780677
31	CEBPB	chr2:9780486-9780817	HepG2	liver:	n/a	chr2:9780664-9780675 chr2:9780664-9780677
32	CEBPB	chr2:9780537-9780814	HepG2	liver:	n/a	chr2:9780664-9780675 chr2:9780664-9780677
33	CEBPB	chr2:9780486-9780860	K562	blood:	n/a	chr2:9780664-9780675 chr2:9780664-9780677
34	CEBPB	chr2:9780482-9780867	K562	blood:	n/a	chr2:9780664-9780675 chr2:9780664-9780677
35	CEBPB	chr2:9788002-9788398	HepG2	liver:	n/a	n/a
36	CEBPB	chr2:9788128-9788237	H1-hESC	embryonic stem cell:	n/a	n/a
37	CEBPB	chr2:9788147-9788229	IMR90	lung:	n/a	n/a
38	CEBPB	chr2:9782743-9783161	K562	blood:	n/a	n/a
39	CEBPD	chr2:9782787-9783179	K562	blood:	n/a	n/a
40	CEBPD	chr2:9782813-9783200	K562	blood:	n/a	n/a
41	CHD2	chr2:9778686-9778935	Hela-S3	cervix:	n/a	n/a
42	CREB1	chr2:9780803-9781163	A549	lung:	n/a	n/a
43	CTCF	chr2:9784704-9784877	NHEK	skin:	n/a	n/a
44	CTCF	chr2:9784700-9784850	SAEC	small airway:	n/a	n/a
45	CTCF	chr2:9784680-9784830	HMEC	breast:	n/a	n/a
46	CTCF	chr2:9784660-9784810	HEEpiC	esophagus:	n/a	n/a
47	CTCF	chr2:9784740-9784890	SAEC	small airway:	n/a	n/a
48	CUX1	chr2:9782636-9783142	K562	blood:	n/a	chr2:9783061-9783075
49	CUX1	chr2:9778756-9779165	K562	blood:	n/a	n/a
50	CUX1	chr2:9777722-9777732	GM12878	blood:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:9778686-9778736	MCF10A-Er-Src	breast:	n/a
2	chr2:9778686-9778736	NHDF-neo	bronchial:	n/a
3	chr2:9778686-9778736	Caco-2	colon:	n/a
4	chr2:9778686-9778736	GM19239	blood:	n/a
5	chr2:9778686-9778736	T-47D	breast:	n/a
6	chr2:9778686-9778736	SK-N-MC	brain:	n/a
7	chr2:9778686-9778736	HCT-116	colon:	n/a
8	chr2:9778686-9778736	PrEC	prostate:	n/a
9	chr2:9778686-9778736	ECC-1	luminal epithelium:	n/a
10	chr2:9778686-9778736	SKMC	muscle:	n/a
11	chr2:9778686-9778736	HPAEpiC	pulmonary alveolar:	n/a
12	chr2:9778686-9778736	BJ	skin:	n/a
13	chr2:9778686-9778736	GM06990	blood:	n/a
14	chr2:9778686-9778736	MCF-7	breast:	n/a
15	chr2:9778686-9778736	HUVEC	blood vessel:	n/a
16	chr2:9778686-9778736	AG10803	skin:	n/a
17	chr2:9778686-9778736	AG09319	gingival:	n/a
18	chr2:9778686-9778736	NH-A	brain:	n/a
19	chr2:9778686-9778736	HCF	heart:	n/a
20	chr2:9778686-9778736	BE2_C	brain:	n/a
21	chr2:9778686-9778736	ProgFib	skin:	n/a
22	chr2:9778686-9778736	GM12892	blood:	n/a
23	chr2:9778686-9778736	SAEC	small airway:	n/a
24	chr2:9778686-9778736	AG04450	lung:	fetal
25	chr2:9778686-9778736	IMR90	lung:	fetal
26	chr2:9778686-9778736	CMK	blood:	n/a
27	chr2:9778686-9778736	HIPEpiC	eye:	n/a
28	chr2:9778686-9778736	HRCEpiC	kidney:	n/a
29	chr2:9778686-9778736	GM12891	blood:	n/a
30	chr2:9778686-9778736	K562	blood:	n/a
31	chr2:9778686-9778736	H1-hESC	embryonic stem cell:	embryo
32	chr2:9778686-9778736	SK-N-SH	brain:	n/a
33	chr2:9778686-9778736	NT2-D1	testis:	n/a
34	chr2:9778686-9778736	Hepatocyte	liver:	n/a
35	chr2:9778686-9778736	HEK293	kidney:	embryo
36	chr2:9778686-9778736	HRE	kidney:	n/a
37	chr2:9778686-9778736	HCM	heart:	n/a
38	chr2:9778686-9778736	NB4	blood:	n/a
39	chr2:9778686-9778736	NHBE	bronchial:	n/a
40	chr2:9778686-9778736	HCPEpiC	choroid plexus:	n/a
41	chr2:9778686-9778736	AG09309	skin:	n/a
42	chr2:9778686-9778736	Hela-S3	cervix:	n/a
43	chr2:9778686-9778736	HEEpiC	esophagus:	n/a
44	chr2:9778686-9778736	HRPEpiC	eye:	n/a
45	chr2:9778686-9778736	U87	brain:	n/a
46	chr2:9778686-9778736	HMEC	breast:	n/a
47	chr2:9778686-9778736	AoSMC	blood vessel:	n/a
48	chr2:9778686-9778736	GM12878	blood:	n/a
49	chr2:9778686-9778736	SK-N-SH_RA	brain:	n/a
50	chr2:9778686-9778736	A549	lung:	n/a

(count:36 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:9779400..9780949-chr2:9782818..9785036,2	K562	blood:
2	chr2:9776400..9778601-chr2:9910278..9912270,2	K562	blood:
3	chr2:9776669..9780406-chr2:9782873..9785983,5	MCF-7	breast:
4	chr2:9775999..9777968-chr2:9781245..9783504,2	K562	blood:
5	chr2:9786319..9790295-chr2:9795169..9796873,3	K562	blood:
6	chr2:9779400..9780949-chr2:9782818..9785036,2	K562	blood:
7	chr2:9769023..9772880-chr2:9783334..9787114,8	MCF-7	breast:
8	chr2:9786319..9789288-chr2:9795169..9797264,3	K562	blood:
9	chr2:9774726..9777001-chr2:9783752..9786208,2	MCF-7	breast:
10	chr2:9777094..9779295-chr2:10091033..10093180,2	MCF-7	breast:
11	chr2:9695463..9697852-chr2:9776763..9778612,2	K562	blood:
12	chr2:9695463..9697852-chr2:9775968..9778612,3	K562	blood:
13	chr2:9770340..9772882-chr2:9783880..9785966,3	MCF-7	breast:
14	chr2:9767218..9769003-chr2:9785866..9787851,2	K562	blood:
15	chr2:9780247..9783706-chr2:9899815..9903353,3	K562	blood:
16	chr2:9777475..9780124-chr2:9787300..9789724,2	K562	blood:
17	chr2:9787484..9789200-chr2:9888207..9889729,2	K562	blood:
18	chr2:9730159..9735372-chr2:9781969..9785269,4	K562	blood:
19	chr2:9781325..9786143-chr2:9786474..9789625,5	K562	blood:
20	chr2:9768781..9770412-chr2:9782843..9784568,2	K562	blood:
21	chr2:9782904..9785147-chr2:9789937..9793084,3	K562	blood:
22	chr2:9767473..9774138-chr2:9774735..9780659,16	MCF-7	breast:
23	chr2:9782654..9789334-chr2:9794560..9799702,7	MCF-7	breast:
24	chr2:9787645..9790270-chr2:9840801..9843386,2	K562	blood:
25	chr2:9774003..9777519-chr2:9779253..9781345,3	MCF-7	breast:
26	chr2:9772257..9774601-chr2:9785690..9787486,2	K562	blood:
27	chr2:9613408..9615593-chr2:9784692..9787153,2	MCF-7	breast:
28	chr2:9775999..9777968-chr2:9781245..9783504,2	K562	blood:
29	chr2:9784748..9786815-chr2:9788863..9790895,3	MCF-7	breast:
30	chr2:9770641..9773022-chr2:9781293..9783585,3	MCF-7	breast:
31	chr2:9774003..9777519-chr2:9779253..9781345,3	MCF-7	breast:
32	chr2:9769155..9773590-chr2:9774278..9779571,11	MCF-7	breast:
33	chr2:9782754..9784911-chr2:9790958..9792910,2	K562	blood:
34	chr2:9769623..9772219-chr2:9787562..9790407,4	MCF-7	breast:
35	chr2:9696523..9698235-chr2:9781544..9783668,2	K562	blood:
36	chr2:9781325..9786143-chr2:9786474..9789625,5	K562	blood:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-IAH1-3	chr2:9778900-9779050	NONHSAT069062
2	lnc-IAH1-3	chr2:9778901-9779050	XLOC_001339
3	lnc-IAH1-3	chr2:9781492-9781586	NONHSAT069062
4	lnc-IAH1-3	chr2:9781493-9781586	XLOC_001339

No data

Variant related genes	Relation type
ENSG00000240687	TF binding region
ENSG00000240687	CpG island
ENSG00000134330	chromatin interactions
ENSG00000134308	chromatin interactions
ENSG00000134317	chromatin interactions
ENSG00000271855	chromatin interactions
ENSG00000240687	chromatin interactions
ENSG00000151694	chromatin interactions
ENSG00000243491	chromatin interactions

Extended variants
information (count: 451 )
Associated
traits (count: 56 )

Variant overlapped rSNPs/rCNVs (count:451 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4668626	chr2:9777229-9777230	Weak transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs374275660	chr2:9777268-9777269	Weak transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
3	rs71437672	chr2:9777326-9777327	Weak transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
4	rs532911401	chr2:9777344-9777345	Weak transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
5	rs7564270	chr2:9777378-9777379	Weak transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs147460570	chr2:9777400-9777401	Weak transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
7	rs538258576	chr2:9777401-9777402	Weak transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
8	rs193250719	chr2:9777403-9777404	Weak transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
9	rs528694166	chr2:9777465-9777466	Weak transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
10	rs138379059	chr2:9777514-9777515	Weak transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
11	rs548792967	chr2:9777557-9777558	Weak transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
12	rs568674132	chr2:9777573-9777574	Weak transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
13	rs75981534	chr2:9777602-9777603	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
14	rs377690436	chr2:9777676-9777677	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
15	rs111314529	chr2:9777698-9777699	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
16	rs372533395	chr2:9777704-9777705	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
17	rs371534579	chr2:9777734-9777735	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
18	rs577282396	chr2:9777740-9777741	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
19	rs142989995	chr2:9777746-9777747	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
20	rs370956432	chr2:9777749-9777750	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
21	rs573480712	chr2:9777757-9777758	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
22	rs571973469	chr2:9777775-9777776	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
23	rs79727134	chr2:9777783-9777784	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
24	rs57272676	chr2:9777877-9777878	Weak transcription Enhancers Genic enhancers Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs541761304	chr2:9778006-9778007	Weak transcription Enhancers Genic enhancers Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
26	rs555255999	chr2:9778016-9778017	Weak transcription Enhancers Genic enhancers Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
27	rs185342372	chr2:9778096-9778097	Weak transcription Enhancers Genic enhancers Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
28	rs544095211	chr2:9778103-9778104	Weak transcription Enhancers Genic enhancers Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
29	rs34619301	chr2:9778110-9778111	Weak transcription Enhancers Genic enhancers Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
30	rs370906496	chr2:9778134-9778135	Weak transcription Enhancers Genic enhancers Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
31	rs540310745	chr2:9778169-9778170	Weak transcription Enhancers Genic enhancers Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
32	rs537439631	chr2:9778218-9778219	Weak transcription Enhancers Genic enhancers Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
33	rs557432553	chr2:9778247-9778248	Weak transcription Enhancers Genic enhancers Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
34	rs533067065	chr2:9778273-9778274	Weak transcription Enhancers Genic enhancers Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
35	rs201450135	chr2:9778277-9778278	Weak transcription Enhancers Genic enhancers Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
36	rs117915441	chr2:9778298-9778299	Weak transcription Enhancers Genic enhancers Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
37	rs560232438	chr2:9778299-9778300	Weak transcription Enhancers Genic enhancers Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
38	rs528781705	chr2:9778424-9778425	Enhancers Weak transcription Genic enhancers Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
39	rs187322348	chr2:9778471-9778472	Enhancers Weak transcription Genic enhancers Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
40	rs568684715	chr2:9778503-9778504	Enhancers Weak transcription Genic enhancers Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
41	rs531099250	chr2:9778506-9778507	Enhancers Weak transcription Genic enhancers Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
42	rs550904008	chr2:9778558-9778559	Enhancers Weak transcription Genic enhancers Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
43	rs115617776	chr2:9778591-9778592	Enhancers Weak transcription Genic enhancers Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
44	rs149245428	chr2:9778592-9778593	Enhancers Weak transcription Genic enhancers Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
45	rs567748512	chr2:9778598-9778599	Enhancers Weak transcription Genic enhancers Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
46	rs552939123	chr2:9778599-9778600	Enhancers Weak transcription Genic enhancers Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
47	rs371525310	chr2:9778642-9778643	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs191808213	chr2:9778653-9778654	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs184076095	chr2:9778674-9778675	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs555607754	chr2:9778675-9778676	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:56)

Disease	PMID	Source
Breast cancer	17133270	CNVD
Mental retardation	17847001	CNVD
Glioblastoma multiforme	21080181	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Cancer	20164920	CNVD
Neuroblastoma	21508638	CNVD
Breast cancer	17603634	CNVD
Cancer	16751803	CNVD
Neuroblastoma	16790693	CNVD
Colorectal cancer	16272173	CNVD
Breast cancer	17393978	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Medulloblastoma	21979893	CNVD
Lynch syndrome	18415027	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17387387	CNVD
Neuroblastoma	17533364	CNVD
Neuroblastoma	18923191	CNVD
Endometrial cancer	22040021	CNVD
Adrenal tumor	17535989	CNVD
Breast cancer	21264507	CNVD
Basal cell lymphoma	17053054	CNVD
Medulloblastoma	17522785	CNVD
Cancer	23418310	CNVD
Ewing''s sarcoma	21437220	CNVD
Ependymoma	16718352	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
lymphocytic leukemia	21291569	CNVD
Prostate cancer	18632612	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Bladder cancer	21909424	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Cancer	20164919	CNVD
Hodgkin''s lymphoma	18641027	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Breast cancer	21364760	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Follicular lymphoma	20505157	CNVD
Autism	17483303	CNVD
Breast cancer	21804112	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	22286061	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Glioma	17123091	CNVD
Breast cancer	20409316	CNVD
Multiple myeloma	16616336	CNVD
Myofibroblastic sarcoma	19369631	CNVD

Chromatin state (count:381 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:9771600-9777800	Weak transcription	Lung	lung
2	chr2:9772000-9777800	Weak transcription	Stomach Smooth Muscle	stomach
3	chr2:9772000-9778400	Weak transcription	Rectal Mucosa Donor 29	rectum
4	chr2:9772200-9781800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
5	chr2:9772400-9777600	Weak transcription	Hela-S3	cervix
6	chr2:9772400-9778000	Weak transcription	Right Atrium	heart
7	chr2:9772600-9777600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr2:9772600-9777800	Weak transcription	Left Ventricle	heart
9	chr2:9772800-9777600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
10	chr2:9772800-9780200	Weak transcription	Placenta Amnion	Placenta Amnion
11	chr2:9773000-9777600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
12	chr2:9773000-9777600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
13	chr2:9773000-9778200	Weak transcription	Right Ventricle	heart
14	chr2:9773000-9778400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
15	chr2:9773000-9778400	Weak transcription	Fetal Intestine Small	intestine
16	chr2:9773400-9777600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
17	chr2:9773600-9777400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
18	chr2:9773600-9777600	Weak transcription	Fetal Muscle Trunk	muscle
19	chr2:9773600-9777800	Weak transcription	Placenta	Placenta
20	chr2:9773600-9778000	Weak transcription	Psoas Muscle	Psoas
21	chr2:9773800-9777400	Weak transcription	Fetal Heart	heart
22	chr2:9774200-9777600	Weak transcription	Skeletal Muscle Female	skeletal muscle
23	chr2:9774400-9777800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
24	chr2:9774800-9777400	Weak transcription	A549	lung
25	chr2:9774800-9778200	Weak transcription	Fetal Intestine Large	intestine
26	chr2:9775000-9782800	Weak transcription	H9 Cell Line	embryonic stem cell
27	chr2:9775200-9777600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
28	chr2:9776200-9777800	Enhancers	Brain Hippocampus Middle	brain
29	chr2:9776200-9778000	Enhancers	Brain Anterior Caudate	brain
30	chr2:9776200-9778200	Enhancers	Brain Inferior Temporal Lobe	brain
31	chr2:9776400-9777600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
32	chr2:9776400-9778400	Enhancers	Brain Cingulate Gyrus	brain
33	chr2:9776400-9779600	Enhancers	Brain Substantia Nigra	brain
34	chr2:9776400-9782000	Enhancers	HMEC	breast
35	chr2:9776600-9779400	Enhancers	Brain Angular Gyrus	brain
36	chr2:9776600-9780200	Enhancers	HSMM	muscle
37	chr2:9776600-9781200	Enhancers	NHDF-Ad	bronchial
38	chr2:9776800-9778000	Weak transcription	Gastric	stomach
39	chr2:9776800-9779000	Enhancers	Muscle Satellite Cultured Cells	--
40	chr2:9776800-9779000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
41	chr2:9776800-9779000	Enhancers	NHLF	lung
42	chr2:9776800-9779800	Enhancers	Osteobl	bone
43	chr2:9776800-9780000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
44	chr2:9776800-9780600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
45	chr2:9776800-9780600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
46	chr2:9776800-9781000	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
47	chr2:9777000-9778400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
48	chr2:9777000-9778800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
49	chr2:9777000-9779400	Enhancers	NHEK	skin
50	chr2:9777000-9779600	Enhancers	Skeletal Muscle Male	skeletal muscle

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