Variant report

Variant	esv3395022
Chromosome Location	chr2:11316915-11426380
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1046)
CpG islands
(count:366)
Chromatin interactive
region (count:96)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:8)

(count:1046 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:11401273-11401437	K562	blood:	n/a	n/a
2	ARID3A	chr2:11376454-11376678	K562	blood:	n/a	n/a
3	ARID3A	chr2:11414239-11414545	K562	blood:	n/a	n/a
4	ARID3A	chr2:11380218-11380597	HepG2	liver:	n/a	n/a
5	ARID3A	chr2:11368718-11369237	K562	blood:	n/a	n/a
6	ARID3A	chr2:11394130-11394529	HepG2	liver:	n/a	n/a
7	ARID3A	chr2:11413824-11413997	K562	blood:	n/a	n/a
8	ARID3A	chr2:11327326-11327740	K562	blood:	n/a	n/a
9	ARID3A	chr2:11374530-11374884	HepG2	liver:	n/a	n/a
10	ARID3A	chr2:11419261-11420073	K562	blood:	n/a	n/a
11	ARID3A	chr2:11374439-11374962	K562	blood:	n/a	n/a
12	ATF1	chr2:11380354-11380556	K562	blood:	n/a	n/a
13	ATF1	chr2:11376445-11376763	K562	blood:	n/a	n/a
14	ATF1	chr2:11419498-11419968	K562	blood:	n/a	n/a
15	ATF1	chr2:11327292-11327633	K562	blood:	n/a	n/a
16	ATF3	chr2:11327245-11327650	K562	blood:	n/a	n/a
17	ATF3	chr2:11376358-11376767	K562	blood:	n/a	n/a
18	BACH1	chr2:11419436-11419654	K562	blood:	n/a	n/a
19	BACH1	chr2:11376758-11376850	K562	blood:	n/a	n/a
20	BATF	chr2:11343619-11343969	GM12878	blood:	n/a	chr2:11343822-11343833 chr2:11343823-11343833
21	BATF	chr2:11343649-11343964	GM12878	blood:	n/a	chr2:11343822-11343833 chr2:11343823-11343833
22	BATF	chr2:11377213-11377527	GM12878	blood:	n/a	chr2:11377395-11377406
23	BCL3	chr2:11343442-11344220	A549	lung:	n/a	n/a
24	BHLHE40	chr2:11327328-11327597	K562	blood:	n/a	n/a
25	BHLHE40	chr2:11343610-11343841	GM12878	blood:	n/a	chr2:11343696-11343705 chr2:11343690-11343711 chr2:11343696-11343705
26	BHLHE40	chr2:11419680-11419901	K562	blood:	n/a	n/a
27	BHLHE40	chr2:11415460-11415682	GM12878	blood:	n/a	n/a
28	BHLHE40	chr2:11343527-11343943	K562	blood:	n/a	chr2:11343696-11343705 chr2:11343690-11343711 chr2:11343696-11343705
29	BHLHE40	chr2:11380223-11380553	K562	blood:	n/a	n/a
30	CBX3	chr2:11402557-11402864	K562	blood:	n/a	n/a
31	CBX3	chr2:11343491-11344130	HCT-116	colon:	n/a	n/a
32	CBX3	chr2:11380066-11380766	HCT-116	colon:	n/a	n/a
33	CBX3	chr2:11376387-11376770	K562	blood:	n/a	n/a
34	CCNT2	chr2:11413906-11414098	K562	blood:	n/a	n/a
35	CCNT2	chr2:11327318-11327558	K562	blood:	n/a	n/a
36	CCNT2	chr2:11419541-11419881	K562	blood:	n/a	n/a
37	CEBPB	chr2:11356272-11356665	A549	lung:	n/a	chr2:11356480-11356491 chr2:11356406-11356417
38	CEBPB	chr2:11350396-11350647	K562	blood:	n/a	chr2:11350501-11350512
39	CEBPB	chr2:11327313-11327708	A549	lung:	n/a	n/a
40	CEBPB	chr2:11318431-11318787	HepG2	liver:	n/a	n/a
41	CEBPB	chr2:11350386-11350667	IMR90	lung:	n/a	chr2:11350501-11350512
42	CEBPB	chr2:11419378-11419937	K562	blood:	n/a	n/a
43	CEBPB	chr2:11356385-11356537	K562	blood:	n/a	chr2:11356480-11356491 chr2:11356406-11356417
44	CEBPB	chr2:11356227-11356806	ECC-1	luminal epithelium:	n/a	chr2:11356480-11356491 chr2:11356406-11356417
45	CEBPB	chr2:11356400-11356561	HepG2	liver:	n/a	chr2:11356480-11356491 chr2:11356406-11356417
46	CEBPB	chr2:11394124-11394568	HepG2	liver:	n/a	n/a
47	CEBPB	chr2:11318349-11318572	A549	lung:	n/a	n/a
48	CEBPB	chr2:11332886-11333266	IMR90	lung:	n/a	chr2:11333201-11333212
49	CEBPB	chr2:11332859-11333247	HepG2	liver:	n/a	chr2:11333201-11333212
50	CEBPB	chr2:11327233-11327768	K562	blood:	n/a	chr2:11327721-11327734

(count:366 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:11397475-11397525	NT2-D1	testis:	n/a
2	chr2:11318465-11318515	A549	lung:	n/a
3	chr2:11318465-11318515	HL-60	blood:	n/a
4	chr2:11397475-11397525	SKMC	muscle:	n/a
5	chr2:11318465-11318515	PFSK-1	brain:	n/a
6	chr2:11364202-11364252	H1-hESC	embryonic stem cell:	embryo
7	chr2:11397475-11397525	BE2_C	brain:	n/a
8	chr2:11364202-11364252	MCF10A-Er-Src	breast:	n/a
9	chr2:11364202-11364252	HCT-116	colon:	n/a
10	chr2:11318465-11318515	AG04449	skin:	fetal
11	chr2:11364202-11364252	NHDF-neo	bronchial:	n/a
12	chr2:11321920-11321970	HepG2	liver:	n/a
13	chr2:11344248-11344298	PANC-1	pancreas:	n/a
14	chr2:11397475-11397525	HEK293	kidney:	embryo
15	chr2:11344248-11344298	T-47D	breast:	n/a
16	chr2:11321920-11321970	AG04449	skin:	fetal
17	chr2:11364202-11364252	AG10803	skin:	n/a
18	chr2:11364202-11364252	NH-A	brain:	n/a
19	chr2:11364202-11364252	MCF-7	breast:	n/a
20	chr2:11397475-11397525	AG10803	skin:	n/a
21	chr2:11397475-11397525	AG04449	skin:	fetal
22	chr2:11318465-11318515	AG04450	lung:	fetal
23	chr2:11344248-11344298	ProgFib	skin:	n/a
24	chr2:11364202-11364252	GM12891	blood:	n/a
25	chr2:11397351-11397401	HPAEpiC	pulmonary alveolar:	n/a
26	chr2:11397351-11397401	K562	blood:	n/a
27	chr2:11397475-11397525	HCF	heart:	n/a
28	chr2:11397475-11397525	AG04450	lung:	fetal
29	chr2:11318465-11318515	GM19239	blood:	n/a
30	chr2:11397351-11397401	Caco-2	colon:	n/a
31	chr2:11397475-11397525	BJ	skin:	n/a
32	chr2:11397475-11397525	AoSMC	blood vessel:	n/a
33	chr2:11397351-11397401	HRE	kidney:	n/a
34	chr2:11321920-11321970	SKMC	muscle:	n/a
35	chr2:11364202-11364252	HL-60	blood:	n/a
36	chr2:11364202-11364252	HCPEpiC	choroid plexus:	n/a
37	chr2:11397351-11397401	T-47D	breast:	n/a
38	chr2:11344248-11344298	Jurkat	blood:	n/a
39	chr2:11318465-11318515	PrEC	prostate:	n/a
40	chr2:11344248-11344298	H1-hESC	embryonic stem cell:	embryo
41	chr2:11318465-11318515	AG09319	gingival:	n/a
42	chr2:11344248-11344298	MCF-7	breast:	n/a
43	chr2:11321920-11321970	A549	lung:	n/a
44	chr2:11364202-11364252	SK-N-MC	brain:	n/a
45	chr2:11321920-11321970	HRPEpiC	eye:	n/a
46	chr2:11321920-11321970	HRE	kidney:	n/a
47	chr2:11318465-11318515	Caco-2	colon:	n/a
48	chr2:11397351-11397401	SK-N-SH	brain:	n/a
49	chr2:11321920-11321970	HRCEpiC	kidney:	n/a
50	chr2:11318465-11318515	HCPEpiC	choroid plexus:	n/a

(count:96 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr2:11325707..11330168-chr2:11330968..11335398,4	MCF-7	breast:
2	chr2:11329062..11332354-chr2:11333253..11335976,4	K562	blood:
3	chr2:11315684..11318531-chr2:11354814..11356618,2	K562	blood:
4	chr2:11354402..11356074-chr2:11357553..11360468,2	K562	blood:
5	chr2:11358381..11360784-chr2:11365018..11367149,2	K562	blood:
6	chr2:11365381..11369172-chr2:11380510..11384403,4	K562	blood:
7	chr2:11410844..11413119-chr2:11416854..11418715,2	K562	blood:
8	chr2:11332757..11334427-chr2:11336977..11338604,2	MCF-7	breast:
9	chr2:11370326..11372790-chr2:11376306..11379258,2	MCF-7	breast:
10	chr2:11405281..11407608-chr2:11412695..11415283,2	K562	blood:
11	chr2:11327523..11329314-chr2:11335510..11337829,2	K562	blood:
12	chr2:11344031..11345866-chr2:11345894..11347764,2	K562	blood:
13	chr2:11422735..11425372-chr2:11448792..11450664,2	MCF-7	breast:
14	chr2:11352617..11354469-chr2:11357510..11359510,2	MCF-7	breast:
15	chr2:11327523..11329314-chr2:11335510..11337829,2	K562	blood:
16	chr2:11317175..11318147-chr2:11325991..11326847,2	K562	blood:
17	chr2:11425026..11427134-chr2:11483302..11485357,2	K562	blood:
18	chr2:11317175..11318147-chr2:11325991..11326847,2	K562	blood:
19	chr2:11378197..11380031-chr2:11396489..11398532,2	K562	blood:
20	chr2:11382499..11384208-chr2:11387400..11389311,2	K562	blood:
21	chr2:11420998..11422528-chr2:11427283..11429692,2	K562	blood:
22	chr2:11349075..11351765-chr2:11482312..11484696,2	K562	blood:
23	chr2:11332757..11334427-chr2:11336977..11338604,2	MCF-7	breast:
24	chr2:11394169..11396145-chr2:11484229..11486145,2	MCF-7	breast:
25	chr2:11376107..11377665-chr2:11385146..11388088,2	K562	blood:
26	chr2:11371027..11372788-chr2:11373923..11376160,2	K562	blood:
27	chr2:11343484..11345478-chr2:11346697..11348958,2	MCF-7	breast:
28	chr2:11318764..11322835-chr2:11322965..11327075,5	MCF-7	breast:
29	chr2:11337630..11339492-chr2:11341637..11343755,2	MCF-7	breast:
30	chr2:11297321..11299192-chr2:11354600..11357317,2	MCF-7	breast:
31	chr2:11336489..11338486-chr2:11405089..11406642,2	K562	blood:
32	chr2:11358381..11364018-chr2:11364236..11368158,7	K562	blood:
33	chr2:11374624..11376647-chr2:11381201..11383592,2	MCF-7	breast:
34	chr2:11352244..11354287-chr2:11354655..11356392,2	K562	blood:
35	chr2:11361664..11363865-chr2:11483951..11486534,2	K562	blood:
36	chr2:11335792..11337450-chr2:11368534..11370356,2	MCF-7	breast:
37	chr2:11315684..11318531-chr2:11354814..11356618,2	K562	blood:
38	chr2:11314637..11317626-chr2:11321207..11322858,2	K562	blood:
39	chr2:11324301..11325954-chr2:11330444..11332305,2	K562	blood:
40	chr2:11367713..11369217-chr2:11376432..11379239,2	K562	blood:
41	chr2:11334066..11335931-chr2:11342091..11344268,2	MCF-7	breast:
42	chr2:11365433..11366937-chr2:11373686..11375238,2	MCF-7	breast:
43	chr2:11380163..11381910-chr2:11382008..11384131,2	MCF-7	breast:
44	chr2:11420942..11423564-chr2:11424238..11426360,2	K562	blood:
45	chr2:11407368..11409021-chr2:11484083..11485849,2	K562	blood:
46	chr2:11410844..11413119-chr2:11416854..11418715,2	K562	blood:
47	chr2:11375000..11377998-chr2:11380925..11383500,2	MCF-7	breast:
48	chr2:11376107..11377665-chr2:11385146..11388088,2	K562	blood:
49	chr2:11411018..11413119-chr2:11416854..11418915,2	K562	blood:
50	chr2:11352244..11354287-chr2:11354655..11356392,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PQLC3-2	chr2:11402605-11403266	l_1777_chr2:11402604-11406864_testes
2	lnc-PQLC3-2	chr2:11406634-11406864	l_1777_chr2:11402604-11406864_testes

No data

(count:8 , 50 per page) page: 1

No.	miRNA target gene	miRNA name	Chromosome Location
1	ROCK2	hsa-miR-124-3p	chr2:11322823-11322817
2	PQLC3	hsa-miR-9-5p	chr2:11318057-11318078
3	PQLC3	hsa-miR-124-3p	chr2:11318562-11318569
4	ROCK2	hsa-miR-138-5p	chr2:11323200-11323222
5	ROCK2	hsa-miR-124-3p	chr2:11322818-11322837
6	PQLC3	hsa-miR-124-3p	chr2:11318550-11318569
7	PQLC3	hsa-miR-9-5p	chr2:11317982-11318004
8	ROCK2	hsa-miR-138-5p	chr2:11323206-11323199

Variant related genes	Relation type
RNU6-1081P	TF binding region
ROCK2	TF binding region
RNU6-1081P	CpG island
ROCK2	CpG island
ENSG00000230952	chromatin interactions
ENSG00000162976	chromatin interactions
ENSG00000134318	chromatin interactions
ENSG00000207267	chromatin interactions

Extended variants
information (count: 3953 )
Associated
traits (count: 65 )

Variant overlapped rSNPs/rCNVs (count:3953 , 50 per page) page: 1 2 3 4 5 6 7 ... 80

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs564638185	chr2:11316945-11316946	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs201456513	chr2:11316999-11317000	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs140966776	chr2:11317016-11317017	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs375359578	chr2:11317017-11317018	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs78891434	chr2:11317018-11317019	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs77557860	chr2:11317019-11317020	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs189303969	chr2:11317057-11317058	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs72785460	chr2:11317075-11317076	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs538159485	chr2:11317077-11317078	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs180837740	chr2:11317097-11317098	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs574974149	chr2:11317101-11317102	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs562880123	chr2:11317122-11317123	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs554735393	chr2:11317128-11317129	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs72785462	chr2:11317159-11317160	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs76633763	chr2:11317193-11317194	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs13013289	chr2:11317197-11317198	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs13013296	chr2:11317209-11317210	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs562532387	chr2:11317220-11317221	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs13018466	chr2:11317226-11317227	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
20	rs548101745	chr2:11317227-11317228	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs564897852	chr2:11317311-11317312	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs145057466	chr2:11317333-11317334	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs544217609	chr2:11317361-11317362	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs138914097	chr2:11317402-11317403	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs13013760	chr2:11317437-11317438	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs548261340	chr2:11317456-11317457	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs560178484	chr2:11317459-11317460	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs114895121	chr2:11317465-11317466	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs13013938	chr2:11317483-11317484	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
30	rs535568742	chr2:11317492-11317493	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs570767838	chr2:11317495-11317496	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs538520498	chr2:11317534-11317535	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs143783217	chr2:11317554-11317555	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs371498449	chr2:11317582-11317583	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs386389533	chr2:11317599-11317600	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs200083995	chr2:11317600-11317601	Weak transcription ZNF genes & repeats Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs369587453	chr2:11317666-11317667	Weak transcription ZNF genes & repeats Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs111696482	chr2:11317750-11317751	Weak transcription ZNF genes & repeats Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs34947693	chr2:11317756-11317757	Weak transcription ZNF genes & repeats Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs79760617	chr2:11317758-11317759	Weak transcription ZNF genes & repeats Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs572950051	chr2:11317764-11317765	Weak transcription ZNF genes & repeats Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs148134570	chr2:11317786-11317787	Weak transcription ZNF genes & repeats Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs113709251	chr2:11317809-11317810	Weak transcription ZNF genes & repeats Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs186189711	chr2:11317812-11317813	Weak transcription ZNF genes & repeats Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs376704717	chr2:11317821-11317822	Weak transcription ZNF genes & repeats Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs200895464	chr2:11317822-11317823	Weak transcription ZNF genes & repeats Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs200178209	chr2:11317826-11317827	Weak transcription ZNF genes & repeats Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs549499330	chr2:11317843-11317844	Weak transcription ZNF genes & repeats Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs142021259	chr2:11317845-11317846	Weak transcription ZNF genes & repeats Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs138558048	chr2:11317922-11317923	Weak transcription ZNF genes & repeats Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:65)

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
Esophageal adenocarcinoma	18519675	CNVD
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:2616 , 50 per page) page: 1 2 3 4 5 6 7 ... 53

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:11296200-11329400	Weak transcription	Gastric	stomach
2	chr2:11296200-11412600	Weak transcription	Aorta	Aorta
3	chr2:11296400-11318800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr2:11296600-11319200	Weak transcription	Fetal Lung	lung
5	chr2:11296800-11318200	Weak transcription	A549	lung
6	chr2:11296800-11379800	Weak transcription	Small Intestine	intestine
7	chr2:11297600-11394400	Weak transcription	Right Ventricle	heart
8	chr2:11298200-11317600	Weak transcription	Fetal Brain Male	brain
9	chr2:11299200-11357000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
10	chr2:11301400-11330400	Weak transcription	Skeletal Muscle Male	skeletal muscle
11	chr2:11301800-11324600	Weak transcription	Primary B cells from cord blood	blood
12	chr2:11302400-11321400	Weak transcription	Fetal Intestine Small	intestine
13	chr2:11302400-11326200	Weak transcription	Fetal Muscle Trunk	muscle
14	chr2:11302400-11335600	Weak transcription	Lung	lung
15	chr2:11304200-11317800	Weak transcription	Fetal Muscle Leg	muscle
16	chr2:11304400-11317800	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
17	chr2:11304400-11321400	Weak transcription	Esophagus	oesophagus
18	chr2:11304400-11321400	Weak transcription	Fetal Stomach	stomach
19	chr2:11304400-11325200	Weak transcription	Stomach Smooth Muscle	stomach
20	chr2:11304400-11326400	Weak transcription	Colon Smooth Muscle	Colon
21	chr2:11304400-11329200	Weak transcription	Duodenum Smooth Muscle	Duodenum
22	chr2:11309800-11318200	Weak transcription	Placenta	Placenta
23	chr2:11309800-11327200	Weak transcription	K562	blood
24	chr2:11309800-11335600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
25	chr2:11310000-11319200	Weak transcription	Adipose Nuclei	Adipose
26	chr2:11310000-11337200	Weak transcription	Ovary	ovary
27	chr2:11310600-11317800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
28	chr2:11310600-11433000	Weak transcription	Pancreas	Pancrea
29	chr2:11312800-11319400	Weak transcription	Fetal Intestine Large	intestine
30	chr2:11313800-11319000	Weak transcription	Rectal Mucosa Donor 29	rectum
31	chr2:11314000-11318000	Weak transcription	Fetal Kidney	kidney
32	chr2:11314000-11318400	Enhancers	Primary monocytes fromperipheralblood	blood
33	chr2:11314000-11318400	Weak transcription	HepG2	liver
34	chr2:11314600-11329600	Weak transcription	Placenta Amnion	Placenta Amnion
35	chr2:11314600-11332200	Weak transcription	Colonic Mucosa	Colon
36	chr2:11314600-11364200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
37	chr2:11314800-11321400	Weak transcription	Sigmoid Colon	Sigmoid Colon
38	chr2:11315000-11317400	Enhancers	Dnd41	blood
39	chr2:11315600-11317600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
40	chr2:11315600-11319200	Weak transcription	Rectal Mucosa Donor 31	rectum
41	chr2:11315600-11319400	Weak transcription	Skeletal Muscle Female	skeletal muscle
42	chr2:11315600-11321600	Weak transcription	Duodenum Mucosa	Duodenum
43	chr2:11315800-11317800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
44	chr2:11315800-11318200	Weak transcription	Brain Angular Gyrus	brain
45	chr2:11315800-11318200	Weak transcription	Brain Inferior Temporal Lobe	brain
46	chr2:11315800-11320000	Weak transcription	Left Ventricle	heart
47	chr2:11315800-11321800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
48	chr2:11315800-11322000	Weak transcription	Brain Hippocampus Middle	brain
49	chr2:11315800-11322800	Weak transcription	Fetal Thymus	thymus
50	chr2:11315800-11326400	Weak transcription	Primary T cells fromperipheralblood	blood

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