Variant report

Variant	nsv537364
Chromosome Location	chr4:175656538-176055348
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1589)
CpG islands
(count:1770)
Chromatin interactive
region (count:81)
LncRNA
region (count:35)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1589 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr4:175976247-175976507	H1-hESC	embryonic stem cell:	n/a	n/a
2	ATF3	chr4:175696587-175696880	K562	blood:	n/a	n/a
3	BACH1	chr4:175750632-175750818	K562	blood:	n/a	n/a
4	BACH1	chr4:175750407-175750888	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr4:175706685-175706779	K562	blood:	n/a	n/a
6	BATF	chr4:175850087-175850349	GM12878	blood:	n/a	n/a
7	BATF	chr4:175957127-175957462	GM12878	blood:	n/a	n/a
8	BATF	chr4:175803802-175804005	GM12878	blood:	n/a	n/a
9	BCL11A	chr4:175955152-175955423	H1-hESC	embryonic stem cell:	n/a	n/a
10	BCL11A	chr4:175849333-175849694	GM12878	blood:	n/a	n/a
11	BCL11A	chr4:175850093-175850258	GM12878	blood:	n/a	n/a
12	BHLHE40	chr4:175828637-175828923	GM12878	blood:	n/a	n/a
13	BHLHE40	chr4:175854210-175854594	GM12878	blood:	n/a	n/a
14	BHLHE40	chr4:175849226-175850369	GM12878	blood:	n/a	n/a
15	BHLHE40	chr4:175684701-175685226	GM12878	blood:	n/a	chr4:175684860-175684869 chr4:175684860-175684869 chr4:175684854-175684875
16	CBX3	chr4:175749887-175750279	K562	blood:	n/a	n/a
17	CBX3	chr4:175828740-175829078	HCT-116	colon:	n/a	n/a
18	CBX3	chr4:175828717-175829001	K562	blood:	n/a	n/a
19	CBX3	chr4:175666036-175666270	K562	blood:	n/a	n/a
20	CBX3	chr4:175828689-175828929	K562	blood:	n/a	n/a
21	CEBPB	chr4:175742727-175742984	A549	lung:	n/a	chr4:175742821-175742832
22	CEBPB	chr4:175917243-175917514	Hela-S3	cervix:	n/a	chr4:175917377-175917388
23	CEBPB	chr4:176048543-176048916	IMR90	lung:	n/a	n/a
24	CEBPB	chr4:176048551-176049015	A549	lung:	n/a	n/a
25	CEBPB	chr4:175709863-175710099	HepG2	liver:	n/a	chr4:175709985-175709996
26	CEBPB	chr4:175742714-175742960	IMR90	lung:	n/a	chr4:175742821-175742832
27	CEBPB	chr4:175917202-175917530	A549	lung:	n/a	chr4:175917377-175917388
28	CEBPB	chr4:176048506-176048915	Hela-S3	cervix:	n/a	n/a
29	CEBPB	chr4:175917251-175917563	IMR90	lung:	n/a	chr4:175917377-175917388
30	CEBPB	chr4:175777349-175777510	HepG2	liver:	n/a	n/a
31	CEBPB	chr4:175922483-175922749	HepG2	liver:	n/a	chr4:175922582-175922593
32	CEBPB	chr4:175834673-175835085	Hela-S3	cervix:	n/a	n/a
33	CEBPB	chr4:175897464-175897664	HepG2	liver:	n/a	chr4:175897610-175897621
34	CEBPB	chr4:175902548-175902769	HepG2	liver:	n/a	chr4:175902691-175902702
35	CEBPB	chr4:175710957-175711166	K562	blood:	n/a	chr4:175711046-175711057
36	CEBPB	chr4:175742736-175742981	HepG2	liver:	n/a	chr4:175742821-175742832
37	CEBPB	chr4:176008342-176008497	A549	lung:	n/a	n/a
38	CEBPB	chr4:176048476-176048980	MCF-7	breast:	n/a	n/a
39	CEBPB	chr4:176008290-176008888	Hela-S3	cervix:	n/a	n/a
40	CEBPB	chr4:175683010-175683286	HepG2	liver:	n/a	n/a
41	CEBPB	chr4:175848165-175848483	MCF-7	breast:	n/a	n/a
42	CEBPB	chr4:175722200-175722428	HepG2	liver:	n/a	chr4:175722305-175722316
43	CEBPB	chr4:175922456-175922766	A549	lung:	n/a	chr4:175922582-175922593
44	CEBPB	chr4:175791814-175792305	MCF-7	breast:	n/a	n/a
45	CEBPB	chr4:175917168-175917537	HepG2	liver:	n/a	chr4:175917377-175917388
46	CEBPB	chr4:176050007-176050304	MCF-7	breast:	n/a	n/a
47	CEBPB	chr4:175715749-175716194	A549	lung:	n/a	n/a
48	CEBPB	chr4:175805720-175805999	A549	lung:	n/a	chr4:175805838-175805849
49	CEBPB	chr4:175683068-175683260	K562	blood:	n/a	n/a
50	CEBPB	chr4:175805695-175805993	IMR90	lung:	n/a	chr4:175805838-175805849

(count:1770 , 50 per page) page: 1 2 3 4 5 6 7 ... 36

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:175750583-175750633	Jurkat	blood:	n/a
2	chr4:175750583-175750633	Jurkat	blood:	n/a
3	chr4:175750510-175750560	HEEpiC	esophagus:	n/a
4	chr4:175851061-175851111	PrEC	prostate:	n/a
5	chr4:175895177-175895227	AG09309	skin:	n/a
6	chr4:175750583-175750633	A549	lung:	n/a
7	chr4:175841091-175841141	A549	lung:	n/a
8	chr4:175751001-175751051	BE2_C	brain:	n/a
9	chr4:175839610-175839660	NH-A	brain:	n/a
10	chr4:175752781-175752831	NB4	blood:	n/a
11	chr4:175838768-175838818	AG04450	lung:	fetal
12	chr4:175750373-175750423	A549	lung:	n/a
13	chr4:175750510-175750560	Hepatocyte	liver:	n/a
14	chr4:175839468-175839518	Hepatocyte	liver:	n/a
15	chr4:175899203-175899253	HCM	heart:	n/a
16	chr4:175789139-175789189	NHBE	bronchial:	n/a
17	chr4:175752781-175752831	AG04450	lung:	fetal
18	chr4:175752696-175752746	HAEpiC	amniotic membrane:	n/a
19	chr4:175838768-175838818	HRE	kidney:	n/a
20	chr4:175750280-175750330	AG09319	gingival:	n/a
21	chr4:175750792-175750842	PANC-1	pancreas:	n/a
22	chr4:175899203-175899253	BE2_C	brain:	n/a
23	chr4:175750109-175750159	AG10803	skin:	n/a
24	chr4:175751001-175751051	HRE	kidney:	n/a
25	chr4:175897327-175897377	ProgFib	skin:	n/a
26	chr4:175750373-175750423	HIPEpiC	eye:	n/a
27	chr4:175750637-175750687	H1-hESC	embryonic stem cell:	embryo
28	chr4:175751001-175751051	HUVEC	blood vessel:	n/a
29	chr4:175750583-175750633	Hela-S3	cervix:	n/a
30	chr4:175750109-175750159	Hela-S3	cervix:	n/a
31	chr4:175750527-175750577	U87	brain:	n/a
32	chr4:175750373-175750423	NHDF-neo	bronchial:	n/a
33	chr4:175838768-175838818	CMK	blood:	n/a
34	chr4:175887842-175887892	BE2_C	brain:	n/a
35	chr4:175887842-175887892	T-47D	breast:	n/a
36	chr4:175839610-175839660	GM12892	blood:	n/a
37	chr4:175887842-175887892	HEEpiC	esophagus:	n/a
38	chr4:175839468-175839518	NHBE	bronchial:	n/a
39	chr4:175839610-175839660	AG09309	skin:	n/a
40	chr4:175750373-175750423	PANC-1	pancreas:	n/a
41	chr4:175750637-175750687	T-47D	breast:	n/a
42	chr4:175752696-175752746	IMR90	lung:	fetal
43	chr4:175750510-175750560	ECC-1	luminal epithelium:	n/a
44	chr4:175851052-175851102	HCF	heart:	n/a
45	chr4:175751001-175751051	SK-N-SH	brain:	n/a
46	chr4:175841091-175841141	SAEC	small airway:	n/a
47	chr4:175897327-175897377	HAEpiC	amniotic membrane:	n/a
48	chr4:175750373-175750423	AG04449	skin:	fetal
49	chr4:175750373-175750423	ovcar-3	ovarian:	n/a
50	chr4:175750373-175750423	GM12891	blood:	n/a

(count:81 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr4:175741383..175744501-chr4:175747246..175749375,3	MCF-7	breast:
2	chr4:175285862..175286838-chr4:175684965..175685904,3	K562	blood:
3	chr4:175748915..175752438-chr4:176045642..176049781,3	MCF-7	breast:
4	chr4:175696425..175698669-chr4:177241063..177242670,2	K562	blood:
5	chr4:175752218..175753789-chr4:175757146..175759391,2	K562	blood:
6	chr4:175958409..175960663-chr4:175963407..175965862,2	MCF-7	breast:
7	chr4:175670375..175673032-chr4:175674464..175676449,2	K562	blood:
8	chr4:175679569..175681556-chr4:175684065..175686816,2	K562	blood:
9	chr4:175995420..175997562-chr4:176011322..176014056,2	MCF-7	breast:
10	chr4:175660189..175662051-chr4:175663383..175664911,2	MCF-7	breast:
11	chr4:175270741..175272762-chr4:175708411..175710972,2	K562	blood:
12	chr4:175953540..175955188-chr4:175958523..175960278,3	MCF-7	breast:
13	chr4:175795214..175795815-chr4:176031046..176031911,2	MCF-7	breast:
14	chr4:175683417..175685346-chr4:175685840..175688189,2	K562	blood:
15	chr4:175842803..175844474-chr4:175850265..175852682,2	MCF-7	breast:
16	chr4:175659609..175661689-chr4:175672380..175674735,2	MCF-7	breast:
17	chr4:175732826..175734634-chr4:175741566..175744026,2	K562	blood:
18	chr4:175958409..175960663-chr4:175963407..175965862,2	MCF-7	breast:
19	chr4:175654877..175657458-chr4:175659006..175661544,3	K562	blood:
20	chr4:175704753..175706331-chr4:176045956..176047741,2	MCF-7	breast:
21	chr4:175674454..175676539-chr4:175676789..175679624,2	MCF-7	breast:
22	chr4:175654313..175656793-chr4:175658655..175661550,2	MCF-7	breast:
23	chr4:175674454..175676539-chr4:175676789..175679624,2	MCF-7	breast:
24	chr4:175795214..175795815-chr4:176031046..176031911,2	MCF-7	breast:
25	chr4:175953540..175955188-chr4:175958523..175960278,3	MCF-7	breast:
26	chr4:176048578..176050591-chr4:176267899..176270064,2	MCF-7	breast:
27	chr4:175654313..175656793-chr4:175658655..175661550,2	MCF-7	breast:
28	chr4:176020592..176022154-chr4:176025242..176028049,2	MCF-7	breast:
29	chr4:176048708..176050759-chr4:176089315..176091997,2	MCF-7	breast:
30	chr4:175863834..175867164-chr4:175868876..175871904,3	MCF-7	breast:
31	chr4:175889489..175891812-chr4:175895689..175898573,2	MCF-7	breast:
32	chr4:175704753..175706331-chr4:176045956..176047741,2	MCF-7	breast:
33	chr4:175748981..175750610-chr4:176045571..176047946,2	MCF-7	breast:
34	chr4:175750658..175752347-chr4:175791168..175793959,2	MCF-7	breast:
35	chr4:175749505..175752528-chr4:175753322..175755968,3	K562	blood:
36	chr4:176026573..176028520-chr4:176029264..176030958,2	K562	blood:
37	chr4:175794804..175795498-chr4:176173944..176174819,2	MCF-7	breast:
38	chr4:175659609..175661689-chr4:175672380..175674735,2	MCF-7	breast:
39	chr4:175654877..175657458-chr4:175659006..175661544,3	K562	blood:
40	chr4:175863834..175867164-chr4:175868876..175871904,3	MCF-7	breast:
41	chr4:175715901..175718406-chr4:175720738..175723252,2	K562	blood:
42	chr4:175752218..175753789-chr4:175757146..175759391,2	K562	blood:
43	chr4:176045992..176048237-chr4:176117695..176119275,2	MCF-7	breast:
44	chr4:176048440..176050830-chr4:176052961..176055108,2	MCF-7	breast:
45	chr4:175730873..175733814-chr4:175736376..175738792,2	MCF-7	breast:
46	chr4:175999154..176001772-chr4:176134842..176136803,2	MCF-7	breast:
47	chr4:175889489..175891812-chr4:175895689..175898573,2	MCF-7	breast:
48	chr4:176025932..176027653-chr4:176048074..176049904,2	MCF-7	breast:
49	chr4:176025932..176027653-chr4:176048074..176049904,2	MCF-7	breast:
50	chr4:175684995..175685845-chr4:176457861..176458680,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GLRA3-1	chr4:175900489-175900532	ENSG00000250431.1
2	lnc-CEP44-5	chr4:175789966-175790300	XLOC_003789
3	lnc-ADAM29-3	chr4:175681175-175682289	l_2788_chr4:175681174-175687959_placenta
4	lnc-CEP44-5	chr4:175852137-175852549	NONHSAT099331
5	lnc-CEP44-5	chr4:175852137-175852325	NONHSAT099327
6	lnc-CEP44-5	chr4:175756000-175756088	XLOC_003789
7	lnc-CEP44-5	chr4:175777682-175777758	NONHSAT099327
8	lnc-ADAM29-4	chr4:175987394-175987592	ucscGeneNc_uc003iua_1
9	lnc-CEP44-5	chr4:175839509-175839622	NONHSAT099331
10	lnc-CEP44-5	chr4:175796946-175797115	XLOC_003789
11	lnc-CEP44-5	chr4:175802504-175802532	XLOC_003789
12	lnc-GLRA3-1	chr4:175899439-175899532	ENSG00000250431.1
13	lnc-CEP44-5	chr4:175756000-175756088	XLOC_003789
14	lnc-CEP44-5	chr4:175777682-175777760	XLOC_003789
15	lnc-CEP44-5	chr4:175756000-175756088	XLOC_003789
16	lnc-CEP44-5	chr4:175756000-175756088	NONHSAT099327
17	lnc-CEP44-5	chr4:175841838-175841943	NONHSAT099331
18	lnc-ADAM29-3	chr4:175687820-175687959	l_2788_chr4:175681174-175687959_placenta
19	lnc-GLRA3-1	chr4:175898722-175898816	ENSG00000250431.1
20	lnc-CEP44-5	chr4:175752879-175753037	XLOC_003789
21	lnc-CEP44-5	chr4:175789957-175791938	XLOC_003789
22	lnc-ADAM29-4	chr4:175992575-175992663	ucscGeneNc_uc003iua_1
23	lnc-CEP44-5	chr4:175750840-175751017	NONHSAT099327
24	lnc-CEP44-5	chr4:175777682-175777758	XLOC_003789
25	lnc-CEP44-5	chr4:175858084-175858128	NONHSAT099332
26	lnc-CEP44-5	chr4:175750819-175751017	XLOC_003789
27	lnc-CEP44-5	chr4:175789957-175791186	XLOC_003789
28	lnc-ADAM29-4	chr4:176026532-176028513	ucscGeneNc_uc003iua_1
29	lnc-CEP44-5	chr4:175852137-175852454	NONHSAT099332
30	lnc-CEP44-5	chr4:175839526-175839622	NONHSAT099332
31	lnc-ADAM29-2	chr4:175938167-175940365	NONHSAT099336
32	lnc-CEP44-5	chr4:175841838-175841943	NONHSAT099332
33	lnc-ADAM29-3	chr4:175684545-175684634	l_2788_chr4:175681174-175687959_placenta
34	lnc-CEP44-5	chr4:175750876-175751017	XLOC_003789
35	lnc-GLRA3-2	chr4:175844964-175845189	NONHSAT099333

No data

Variant related genes	Relation type
GLRA3	TF binding region
ENSG00000249411	TF binding region
ENSG00000250431	TF binding region
ADAM29	TF binding region
ENSG00000265493	TF binding region
ENSG00000250200	TF binding region
GLRA3	CpG island
ENSG00000249411	CpG island
ENSG00000250431	CpG island
ADAM29	CpG island
ENSG00000265493	CpG island
ENSG00000250200	CpG island
ENSG00000145451	chromatin interactions
ENSG00000168594	chromatin interactions
ENSG00000248980	chromatin interactions
ENSG00000129128	chromatin interactions
ALDH1B1	miRNA target sites
RBM15	miRNA target sites

Extended variants
information (count: 3830 )
Associated
traits (count: 76 )

Variant overlapped rSNPs/rCNVs (count:3830 , 50 per page) page: 1 2 3 4 5 6 7 ... 77

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs183833047	chr4:175663636-175663637	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs542055221	chr4:175663714-175663715	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs555921328	chr4:175663725-175663726	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs7654132	chr4:175663821-175663822	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs528980797	chr4:175663832-175663833	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs370028616	chr4:175663854-175663855	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs111872389	chr4:175663855-175663856	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs544120081	chr4:175663856-175663857	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs76151588	chr4:175663871-175663872	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs540349203	chr4:175663891-175663892	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs529769520	chr4:175663975-175663976	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs556513396	chr4:175665005-175665006	Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs575497883	chr4:175665027-175665028	Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs535590555	chr4:175665044-175665045	Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs369079647	chr4:175665055-175665056	Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs144163276	chr4:175665078-175665079	Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs112341191	chr4:175665090-175665091	Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs28575210	chr4:175665105-175665106	Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs569370521	chr4:175665135-175665136	Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs142387520	chr4:175665140-175665141	Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs149053958	chr4:175665150-175665151	Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs558366152	chr4:175665203-175665204	Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs578259806	chr4:175665217-175665218	Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs6818269	chr4:175665254-175665255	Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs143859916	chr4:175665338-175665339	Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs13110718	chr4:175665339-175665340	Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs386682273	chr4:175665369-175665370	Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs76014598	chr4:175665370-175665371	Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs576042878	chr4:175665404-175665405	Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs545231602	chr4:175665423-175665424	Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs6840689	chr4:175665424-175665425	Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs370723270	chr4:175665491-175665492	Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs373863841	chr4:175665515-175665516	Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs77292740	chr4:175665529-175665530	Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs542360148	chr4:175665530-175665531	Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs148643065	chr4:175665532-175665533	Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs529257278	chr4:175665537-175665538	Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs549083753	chr4:175665550-175665551	Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs569365599	chr4:175665574-175665575	Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs531704193	chr4:175665577-175665578	Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs557797920	chr4:175669807-175669808	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs180907722	chr4:175669818-175669819	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs114122543	chr4:175669837-175669838	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs186010258	chr4:175669868-175669869	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs191159470	chr4:175669892-175669893	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs116850776	chr4:175669908-175669909	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs375073690	chr4:175669974-175669975	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs58011888	chr4:175670015-175670016	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs57501830	chr4:175670016-175670017	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs181921756	chr4:175670042-175670043	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:76)

Disease	PMID	Source
Acute lymphoblastic leukemia	22237106	CNVD
Glioblastoma multiforme	21080181	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Chordoma	21602918	CNVD
HIV/AIDS	22032296	CNVD
Medulloblastoma	21979893	CNVD
Neuroblastoma	18923191	CNVD
Breast cancer	21858162	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Gastric cancer	21586687	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Colorectal cancer	19359472	CNVD
Malignant mesothelioma	18160781	CNVD
Medulloblastoma	18056178	CNVD
Multiple myeloma	17077331	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Oral squamous cell carcinoma	17134496	CNVD
4q-syndrome	17576883	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Colorectal cancer	20709793	CNVD
Muscular dystrophy	21149563	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Cervical cancer	21062161	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	16608533	CNVD
Wilms tumour	21544195	CNVD
Lung cancer	18438408	CNVD
Cancer	22429812	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Breast cancer	16272173	CNVD
Breast cancer	17133270	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Congenital anomalies of the kidney and urinary tract	20505237	CNVD
Testicular germ cell tumor	18059402	CNVD
Ovarian cancer	22174824	CNVD
Olfactory neuroblastoma	18408657	CNVD
Breast cancer	21785460	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Hodgkin''s lymphoma	17606441	CNVD
small cell lung cancer	20016488	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Ewing''s sarcoma	17952124	CNVD
Breast cancer	21633010	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Cancer	20581869	CNVD
Hepatocellular carcinoma	16750200	CNVD
abnormal development	18461090	CNVD
Esophageal squamous carcinoma	17470683	CNVD
Neuroblastoma	16790693	CNVD
Lung cancer	16773561	CNVD
Colorectal cancer	16774939	CNVD
Myelofibrosis	22110671	CNVD
Developmental delay	22127048	CNVD
Glioblastoma multiforme	22286061	CNVD
Neuroblastoma	21899760	CNVD
Gastric adenocarcinoma	19115996	CNVD
Cancer	20164919	CNVD
Prostate cancer	22341455	CNVD
Intellectual disability	21811512	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Glioma	20126413	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:355 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:175663600-175664000	Enhancers	Pancreatic Islets	Pancreatic Islet
2	chr4:175665000-175665600	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr4:175669800-175670800	Enhancers	Breast Myoepithelial Primary Cells	Breast
4	chr4:175670000-175670600	Enhancers	Stomach Smooth Muscle	stomach
5	chr4:175672000-175672200	Enhancers	Pancreatic Islets	Pancreatic Islet
6	chr4:175672200-175673200	Weak transcription	Pancreatic Islets	Pancreatic Islet
7	chr4:175672800-175674400	Enhancers	Fetal Brain Male	brain
8	chr4:175673200-175673400	Enhancers	Pancreatic Islets	Pancreatic Islet
9	chr4:175673400-175674000	Weak transcription	Pancreatic Islets	Pancreatic Islet
10	chr4:175674000-175674200	Active TSS	Pancreatic Islets	Pancreatic Islet
11	chr4:175674200-175674600	Flanking Active TSS	Pancreatic Islets	Pancreatic Islet
12	chr4:175674400-175674800	Weak transcription	Fetal Brain Male	brain
13	chr4:175674600-175675200	Enhancers	Pancreatic Islets	Pancreatic Islet
14	chr4:175674800-175675400	Enhancers	Fetal Brain Male	brain
15	chr4:175675400-175682600	Weak transcription	Fetal Brain Male	brain
16	chr4:175678800-175679200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
17	chr4:175678800-175679600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
18	chr4:175679000-175679200	Enhancers	ES-I3 Cell Line	embryonic stem cell
19	chr4:175679000-175679200	Enhancers	Gastric	stomach
20	chr4:175679000-175679200	Enhancers	K562	blood
21	chr4:175679000-175679400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
22	chr4:175679000-175679400	Enhancers	HUES6 Cell Line	embryonic stem cell
23	chr4:175679000-175679400	Enhancers	Cortex derived primary cultured neurospheres	brain
24	chr4:175679000-175679600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
25	chr4:175679400-175681200	Weak transcription	HUES6 Cell Line	embryonic stem cell
26	chr4:175682600-175683600	Enhancers	Fetal Brain Male	brain
27	chr4:175683000-175684800	Weak transcription	HUES6 Cell Line	embryonic stem cell
28	chr4:175684800-175685400	Enhancers	HUES6 Cell Line	embryonic stem cell
29	chr4:175685200-175685400	Enhancers	Muscle Satellite Cultured Cells	--
30	chr4:175688800-175689400	Enhancers	Breast Myoepithelial Primary Cells	Breast
31	chr4:175696400-175697800	Enhancers	K562	blood
32	chr4:175697800-175698600	Weak transcription	K562	blood
33	chr4:175698600-175698800	Enhancers	K562	blood
34	chr4:175698800-175699200	Weak transcription	K562	blood
35	chr4:175699200-175700000	Active TSS	K562	blood
36	chr4:175699200-175700600	Active TSS	ES-I3 Cell Line	embryonic stem cell
37	chr4:175699400-175699600	Enhancers	HUES64 Cell Line	embryonic stem cell
38	chr4:175699400-175699600	Enhancers	iPS-15b Cell Line	embryonic stem cell
39	chr4:175699400-175700000	Active TSS	ES-WA7 Cell Line	embryonic stem cell
40	chr4:175699400-175700600	Active TSS	HUES6 Cell Line	embryonic stem cell
41	chr4:175699600-175700000	Enhancers	H1 Cell Line	embryonic stem cell
42	chr4:175699600-175700000	Active TSS	iPS-15b Cell Line	embryonic stem cell
43	chr4:175699600-175700200	Active TSS	H9 Cell Line	embryonic stem cell
44	chr4:175699600-175700200	Active TSS	HUES64 Cell Line	embryonic stem cell
45	chr4:175715400-175715800	Enhancers	Pancreatic Islets	Pancreatic Islet
46	chr4:175715400-175715800	Enhancers	A549	lung
47	chr4:175715400-175715800	Enhancers	Hela-S3	cervix
48	chr4:175731200-175731400	Enhancers	iPS-15b Cell Line	embryonic stem cell
49	chr4:175731200-175732200	Enhancers	HUES48 Cell Line	embryonic stem cell
50	chr4:175731400-175732000	Weak transcription	iPS-15b Cell Line	embryonic stem cell

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