Variant report

Variant	nsv830352
Chromosome Location	chr5:74189495-74337944
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1771)
CpG islands
(count:732)
Chromatin interactive
region (count:39)
LncRNA
region (count:19)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1771 , 50 per page) page: 1 2 3 4 5 6 7 ... 36

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr5:74333093-74333098	HepG2	liver:	n/a	n/a
2	ARID3A	chr5:74199250-74199532	HepG2	liver:	n/a	n/a
3	ARID3A	chr5:74250044-74251228	HepG2	liver:	n/a	n/a
4	ARID3A	chr5:74234202-74234415	HepG2	liver:	n/a	n/a
5	ARID3A	chr5:74215018-74215648	HepG2	liver:	n/a	n/a
6	ARID3A	chr5:74306723-74307157	HepG2	liver:	n/a	n/a
7	ARID3A	chr5:74221773-74221800	HepG2	liver:	n/a	n/a
8	ARID3A	chr5:74230706-74231126	HepG2	liver:	n/a	n/a
9	ARID3A	chr5:74293577-74293804	HepG2	liver:	n/a	n/a
10	ARID3A	chr5:74213940-74214467	HepG2	liver:	n/a	n/a
11	ARID3A	chr5:74215365-74215608	K562	blood:	n/a	n/a
12	ARID3A	chr5:74244984-74245309	HepG2	liver:	n/a	n/a
13	ARID3A	chr5:74212565-74213265	HepG2	liver:	n/a	n/a
14	ARID3A	chr5:74242220-74242714	HepG2	liver:	n/a	n/a
15	BACH1	chr5:74230915-74231125	H1-hESC	embryonic stem cell:	n/a	n/a
16	BATF	chr5:74241372-74241684	GM12878	blood:	n/a	n/a
17	BCL11A	chr5:74330662-74330978	GM12878	blood:	n/a	n/a
18	BCL3	chr5:74312708-74313047	GM12878	blood:	n/a	n/a
19	BCL3	chr5:74312620-74313128	GM12878	blood:	n/a	n/a
20	BCLAF1	chr5:74241342-74241682	GM12878	blood:	n/a	n/a
21	BHLHE40	chr5:74199321-74199400	GM12878	blood:	n/a	n/a
22	BHLHE40	chr5:74317260-74317368	K562	blood:	n/a	n/a
23	BHLHE40	chr5:74212289-74213217	HepG2	liver:	n/a	n/a
24	BHLHE40	chr5:74214018-74214392	HepG2	liver:	n/a	n/a
25	BHLHE40	chr5:74250138-74250843	HepG2	liver:	n/a	n/a
26	BRCA1	chr5:74248648-74248659	GM12878	blood:	n/a	n/a
27	CBX3	chr5:74332829-74333508	HCT-116	colon:	n/a	n/a
28	CBX3	chr5:74332824-74333456	HCT-116	colon:	n/a	n/a
29	CEBPB	chr5:74234222-74234272	HepG2	liver:	n/a	n/a
30	CEBPB	chr5:74336811-74337100	Hela-S3	cervix:	n/a	chr5:74336869-74336877 chr5:74336994-74337006
31	CEBPB	chr5:74289427-74289535	K562	blood:	n/a	chr5:74289499-74289512 chr5:74289500-74289511 chr5:74289499-74289510
32	CEBPB	chr5:74285584-74285763	H1-hESC	embryonic stem cell:	n/a	chr5:74285658-74285669
33	CEBPB	chr5:74332997-74333419	ECC-1	luminal epithelium:	n/a	n/a
34	CEBPB	chr5:74212575-74213077	HepG2	liver:	n/a	n/a
35	CEBPB	chr5:74247830-74248008	HepG2	liver:	n/a	n/a
36	CEBPB	chr5:74191824-74192241	ECC-1	luminal epithelium:	n/a	n/a
37	CEBPB	chr5:74330260-74330713	MCF-7	breast:	n/a	n/a
38	CEBPB	chr5:74303202-74303580	IMR90	lung:	n/a	n/a
39	CEBPB	chr5:74212559-74213070	HepG2	liver:	n/a	n/a
40	CEBPB	chr5:74333015-74333324	Hela-S3	cervix:	n/a	n/a
41	CEBPB	chr5:74270726-74270766	HepG2	liver:	n/a	n/a
42	CEBPB	chr5:74211376-74211658	HepG2	liver:	n/a	n/a
43	CEBPB	chr5:74332973-74333392	ECC-1	luminal epithelium:	n/a	n/a
44	CEBPB	chr5:74250128-74250585	Hela-S3	cervix:	n/a	chr5:74250434-74250447 chr5:74250436-74250445
45	CEBPB	chr5:74306875-74307347	HepG2	liver:	n/a	chr5:74307193-74307204
46	CEBPB	chr5:74289343-74289673	IMR90	lung:	n/a	chr5:74289499-74289512 chr5:74289500-74289511 chr5:74289499-74289510
47	CEBPB	chr5:74336777-74337168	IMR90	lung:	n/a	chr5:74336869-74336877 chr5:74336994-74337006
48	CEBPB	chr5:74249780-74251059	IMR90	lung:	n/a	chr5:74250434-74250447 chr5:74250436-74250445
49	CEBPB	chr5:74211479-74211616	A549	lung:	n/a	n/a
50	CEBPB	chr5:74212619-74212989	HepG2	liver:	n/a	n/a

(count:732 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:74303397-74303447	PANC-1	pancreas:	n/a
2	chr5:74330425-74330475	HRCEpiC	kidney:	n/a
3	chr5:74199422-74199472	HMEC	breast:	n/a
4	chr5:74231171-74231221	HUVEC	blood vessel:	n/a
5	chr5:74244655-74244705	HCM	heart:	n/a
6	chr5:74327281-74327331	PANC-1	pancreas:	n/a
7	chr5:74244655-74244705	LNCaP	prostate:	n/a
8	chr5:74330737-74330787	ProgFib	skin:	n/a
9	chr5:74199422-74199472	T-47D	breast:	n/a
10	chr5:74327277-74327327	LNCaP	prostate:	n/a
11	chr5:74331325-74331375	HL-60	blood:	n/a
12	chr5:74327277-74327327	AoSMC	blood vessel:	n/a
13	chr5:74303397-74303447	AG04449	skin:	fetal
14	chr5:74330737-74330787	Caco-2	colon:	n/a
15	chr5:74231171-74231221	U87	brain:	n/a
16	chr5:74328211-74328261	Hepatocyte	liver:	n/a
17	chr5:74199422-74199472	HPAEpiC	pulmonary alveolar:	n/a
18	chr5:74328211-74328261	PrEC	prostate:	n/a
19	chr5:74244655-74244705	H1-hESC	embryonic stem cell:	embryo
20	chr5:74330425-74330475	PrEC	prostate:	n/a
21	chr5:74331325-74331375	SKMC	muscle:	n/a
22	chr5:74330737-74330787	RPTEC	kidney:	n/a
23	chr5:74333288-74333338	AG10803	skin:	n/a
24	chr5:74328211-74328261	LNCaP	prostate:	n/a
25	chr5:74326281-74326331	HCM	heart:	n/a
26	chr5:74333288-74333338	HCPEpiC	choroid plexus:	n/a
27	chr5:74330737-74330787	SK-N-MC	brain:	n/a
28	chr5:74326281-74326331	HAEpiC	amniotic membrane:	n/a
29	chr5:74199422-74199472	AG09319	gingival:	n/a
30	chr5:74231171-74231221	LNCaP	prostate:	n/a
31	chr5:74231171-74231221	GM06990	blood:	n/a
32	chr5:74328211-74328261	HEEpiC	esophagus:	n/a
33	chr5:74244655-74244705	HEEpiC	esophagus:	n/a
34	chr5:74244655-74244705	HRPEpiC	eye:	n/a
35	chr5:74333288-74333338	HL-60	blood:	n/a
36	chr5:74244655-74244705	NH-A	brain:	n/a
37	chr5:74244655-74244705	PrEC	prostate:	n/a
38	chr5:74303397-74303447	K562	blood:	n/a
39	chr5:74199422-74199472	HCM	heart:	n/a
40	chr5:74330425-74330475	K562	blood:	n/a
41	chr5:74231171-74231221	ProgFib	skin:	n/a
42	chr5:74333288-74333338	Hela-S3	cervix:	n/a
43	chr5:74331325-74331375	GM12892	blood:	n/a
44	chr5:74327281-74327331	Caco-2	colon:	n/a
45	chr5:74330425-74330475	BE2_C	brain:	n/a
46	chr5:74328211-74328261	AG09319	gingival:	n/a
47	chr5:74303397-74303447	NT2-D1	testis:	n/a
48	chr5:74244655-74244705	MCF10A-Er-Src	breast:	n/a
49	chr5:74231171-74231221	T-47D	breast:	n/a
50	chr5:74327277-74327327	HNPCEpiC	eye:	n/a

(count:39 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr5:74251721..74254234-chr5:74259787..74261989,3	MCF-7	breast:
2	chr5:74239354..74241176-chr5:74242869..74245249,2	MCF-7	breast:
3	chr5:73979354..73981671-chr5:74212696..74216316,3	MCF-7	breast:
4	chr5:74213877..74216591-chr7:112090452..112092226,2	MCF-7	breast:
5	chr5:74230526..74231383-chr5:74345361..74346008,2	MCF-7	breast:
6	chr5:74245711..74248702-chr5:74259908..74262070,2	MCF-7	breast:
7	chr5:74265415..74267966-chr5:74268550..74270837,2	K562	blood:
8	chr5:74235381..74238008-chr5:74240552..74242250,2	K562	blood:
9	chr5:74315578..74317119-chr5:74341476..74343130,2	MCF-7	breast:
10	chr5:74251721..74254234-chr5:74259787..74261989,3	MCF-7	breast:
11	chr5:73980015..73981765-chr5:74329525..74332329,2	MCF-7	breast:
12	chr5:74331704..74333232-chr5:74343101..74344687,2	MCF-7	breast:
13	chr5:74221093..74221795-chr5:74230378..74230940,2	MCF-7	breast:
14	chr5:74220830..74221511-chr5:74561645..74562178,2	MCF-7	breast:
15	chr5:74315848..74318238-chr5:74328353..74330042,2	MCF-7	breast:
16	chr5:74239354..74241176-chr5:74242869..74245249,2	MCF-7	breast:
17	chr5:73968444..73969362-chr5:74215054..74216242,3	MCF-7	breast:
18	chr5:74332922..74335648-chr5:74338677..74341293,2	MCF-7	breast:
19	chr5:73980895..73982599-chr5:74214365..74217155,2	MCF-7	breast:
20	chr5:74318809..74320982-chr5:74323765..74325406,2	MCF-7	breast:
21	chr5:74266271..74268697-chr5:74331711..74333363,2	MCF-7	breast:
22	chr5:74235381..74238008-chr5:74240552..74242250,2	K562	blood:
23	chr5:74230538..74231300-chr5:74561168..74561757,3	MCF-7	breast:
24	chr11:57561542..57564393-chr5:74329604..74332106,2	MCF-7	breast:
25	chr5:74330454..74335475-chr5:74336350..74340630,5	MCF-7	breast:
26	chr5:74062152..74062829-chr5:74198970..74199641,2	K562	blood:
27	chr5:74220860..74221763-chr5:74345733..74346235,2	MCF-7	breast:
28	chr5:74221093..74221795-chr5:74230378..74230940,2	MCF-7	breast:
29	chr5:74245711..74248702-chr5:74259908..74262070,2	MCF-7	breast:
30	chr5:74334981..74336782-chr5:74342190..74344248,2	MCF-7	breast:
31	chr5:73944427..73945323-chr5:74215021..74215775,2	MCF-7	breast:
32	chr5:74315848..74318238-chr5:74328353..74330042,2	MCF-7	breast:
33	chr5:74330454..74335475-chr5:74336350..74340630,5	MCF-7	breast:
34	chr5:74266271..74268697-chr5:74331711..74333363,2	MCF-7	breast:
35	chr5:74082489..74083391-chr5:74199247..74199809,4	MCF-7	breast:
36	chr5:74265415..74267966-chr5:74268550..74270837,2	K562	blood:
37	chr5:74245978..74248569-chr5:74531357..74534080,2	MCF-7	breast:
38	chr15:87299754..87300537-chr5:74333585..74334466,2	MCF-7	breast:
39	chr5:74230558..74231547-chr5:74561170..74561749,2	MCF-7	breast:

(count:19 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-NSA2-1	chr5:74271427-74271554	XLOC_004430
2	lnc-FAM169A-1	chr5:74195136-74195344	XLOC_004889
3	lnc-GCNT4-2	chr5:74337140-74337513	NONHSAT102193
4	lnc-FAM169A-1	chr5:74199354-74199389	XLOC_004889
5	lnc-GCNT4-3	chr5:74302538-74302837	NONHSAT102192
6	lnc-NSA2-7	chr5:74225705-74226391	NONHSAT102186
7	lnc-NSA2-1	chr5:74244126-74244215	NONHSAT102189
8	lnc-GCNT4-1	chr5:74283326-74283448	ENSG00000249856.1
9	lnc-NSA2-1	chr5:74244126-74244215	FPKM1_group_25626_transcript_1
10	lnc-NSA2-1	chr5:74271426-74271554	NONHSAT102189
11	lnc-GCNT4-1	chr5:74313254-74313367	ENSG00000249856.1
12	lnc-GCNT4-1	chr5:74213551-74213803	ENSG00000249856.1
13	lnc-NSA2-1	chr5:74243952-74244685	NONHSAT102188
14	lnc-NSA2-8	chr5:74279794-74279971	l_2947_chr5:74279793-74307259_76bGuttman_hLF
15	lnc-NSA2-1	chr5:74244399-74244527	FPKM1_group_25626_transcript_1
16	lnc-GCNT4-1	chr5:74214854-74215111	ENSG00000249856.1
17	lnc-GCNT4-1	chr5:74319656-74319753	ENSG00000249856.1
18	lnc-NSA2-8	chr5:74307183-74307310	l_2947_chr5:74279793-74307259_76bGuttman_hLF
19	lnc-NSA2-1	chr5:74244127-74244215	XLOC_004430

No data

Variant related genes	Relation type
GCNT4	TF binding region
ENSG00000249157	TF binding region
RPL27AP5	TF binding region
ENSG00000239517	TF binding region
ENSG00000249856	TF binding region
ENSG00000196390	TF binding region
GCNT4	CpG island
ENSG00000249157	CpG island
RPL27AP5	CpG island
ENSG00000239517	CpG island
ENSG00000249856	CpG island
ENSG00000196390	CpG island
ENSG00000145700	chromatin interactions
ENSG00000049860	chromatin interactions
ENSG00000006652	chromatin interactions
ENSG00000164346	chromatin interactions
ENSG00000249856	chromatin interactions
BCL2	miRNA target sites
USP22	miRNA target sites

Extended variants
information (count: 5057 )
Associated
traits (count: 89 )

Variant overlapped rSNPs/rCNVs (count:5057 , 50 per page) page: 1 2 3 4 5 6 7 ... 102

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs567375346	chr5:74190402-74190403	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
2	rs190719959	chr5:74190443-74190444	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
3	rs142370398	chr5:74190450-74190451	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
4	rs566707697	chr5:74190563-74190564	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
5	rs372982530	chr5:74190680-74190681	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
6	rs377160042	chr5:74190709-74190710	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
7	rs538913529	chr5:74190770-74190771	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
8	rs558859901	chr5:74190771-74190772	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
9	rs575539101	chr5:74190841-74190842	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
10	rs538246182	chr5:74190864-74190865	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
11	rs554718487	chr5:74190875-74190876	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
12	rs574613579	chr5:74190888-74190889	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
13	rs533887008	chr5:74190904-74190905	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
14	rs192184933	chr5:74190926-74190927	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
15	rs577048480	chr5:74190938-74190939	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
16	rs184506302	chr5:74190943-74190944	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
17	rs563208204	chr5:74190951-74190952	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
18	rs539478254	chr5:74190987-74190988	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
19	rs554111113	chr5:74191068-74191069	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs570790672	chr5:74191094-74191095	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs143859024	chr5:74191114-74191115	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs76338690	chr5:74191150-74191151	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs148606715	chr5:74191250-74191251	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs142238894	chr5:74191261-74191262	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs111853460	chr5:74191273-74191274	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs566670450	chr5:74191399-74191400	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs150795649	chr5:74191417-74191418	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs376925009	chr5:74191418-74191419	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs13340369	chr5:74191427-74191428	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs139712808	chr5:74191460-74191461	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs200894495	chr5:74191510-74191511	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs145188435	chr5:74191523-74191524	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs573875483	chr5:74191608-74191609	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs147905684	chr5:74191642-74191643	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs568150541	chr5:74191645-74191646	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs79452729	chr5:74191692-74191693	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs141612846	chr5:74191695-74191696	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs113321865	chr5:74191737-74191738	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs181260314	chr5:74191743-74191744	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs184324158	chr5:74191761-74191762	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs556836846	chr5:74191794-74191795	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs1455786	chr5:74191807-74191808	Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs189016696	chr5:74191810-74191811	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs370974181	chr5:74191893-74191894	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs13340354	chr5:74191976-74191977	Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs539886519	chr5:74191981-74191982	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs149989106	chr5:74192004-74192005	Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
48	rs560848540	chr5:74192009-74192010	Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
49	rs529764333	chr5:74192023-74192024	Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
50	rs540323542	chr5:74192027-74192028	Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:89)

Disease	PMID	Source
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Metanephric adenoma	20802469	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Medulloblastoma	21979893	CNVD
Phyllodes tumor	17334353	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Cancer	16751803	CNVD
Intellectual disability	22102821	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Breast cancer	17603634	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Melanoma	18172304	CNVD
Glioma	20126413	CNVD
Breast cancer	22032731	CNVD
Prostate cancer	21965145	CNVD
Spinal muscular atrophy	21762474	CNVD
Esophageal cancer	20955586	CNVD
Congenital anomalies of the kidney and urinary tract	18694510	CNVD
Ovarian cancer	20844748	CNVD
Breast cancer	17393978	CNVD
Cancer	21359685	CNVD
Non-small cell lung cancer	21829676	CNVD
adenomatous polyposis	22470819	CNVD
Cancer	22429812	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Liposarcoma	21253554	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Breast cancer	21858162	CNVD
Hepatocellular carcinoma	16750200	CNVD
Leukemia	17361228	CNVD
Myelodysplastic syndrome	18508791	CNVD
5q-syndrome	17576883	CNVD
Gastric cancer	17908304	CNVD
Lung cancer	16740712	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Urothelial carcinoma	21177765	CNVD
Oral cancer	21386901	CNVD
Bladder cancer	21909424	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Barrett''s syndrome	19417022	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Breast cancer	19602461	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Retinoblastoma	22278416	CNVD
Bipolar disorder	18458673	CNVD
Thyroid cancer	19087340	CNVD
Breast cancer	21785460	CNVD
Merkel cell carcinoma	19020549	CNVD
Squamous cell cancer	20885788	CNVD
Neurodevelopmental disorder	22521361	CNVD
Prostate cancer	18632612	CNVD
Ovarian cancer	21720365	CNVD
Spinal muscular atrophy	15981080	CNVD
Spinal muscular atrophy	18839960	CNVD
Spinal muscular atrophy	19716110	CNVD
Glioblastoma multiforme	22286061	CNVD
craniofacial dysmorphism	21918468	CNVD
Multiple myeloma	16616336	CNVD
Prostate cancer	16461572	CNVD
Breast cancer	17133270	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Acute myeloid leukemia	20729466	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Ovarian cancer	22355333	CNVD
Acute myeloid leukemia	21251322	CNVD
Myelofibrosis	22110671	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Amyotrophic lateral sclerosis	20685689	CNVD
Melanoma	20877625	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:1235 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:74190400-74191000	ZNF genes & repeats	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr5:74191000-74191800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr5:74191200-74193000	Enhancers	Fetal Brain Female	brain
4	chr5:74191400-74191800	Enhancers	Brain Substantia Nigra	brain
5	chr5:74191400-74192200	Enhancers	Fetal Lung	lung
6	chr5:74191400-74192400	Enhancers	Brain Cingulate Gyrus	brain
7	chr5:74191400-74192400	Enhancers	Fetal Heart	heart
8	chr5:74191600-74191800	Enhancers	Brain Anterior Caudate	brain
9	chr5:74191600-74191800	Enhancers	Brain Hippocampus Middle	brain
10	chr5:74191600-74192200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
11	chr5:74191600-74192200	Enhancers	Stomach Smooth Muscle	stomach
12	chr5:74191600-74192400	Enhancers	Liver	Liver
13	chr5:74191600-74192400	Enhancers	Brain Angular Gyrus	brain
14	chr5:74191600-74192400	Enhancers	Brain Inferior Temporal Lobe	brain
15	chr5:74191600-74192400	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
16	chr5:74191600-74192400	Enhancers	Fetal Brain Male	brain
17	chr5:74191800-74192000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
18	chr5:74191800-74192000	Enhancers	H9 Cell Line	embryonic stem cell
19	chr5:74191800-74192200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
20	chr5:74191800-74192200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
21	chr5:74191800-74192200	Enhancers	Aorta	Aorta
22	chr5:74191800-74192200	Flanking Active TSS	Brain Substantia Nigra	brain
23	chr5:74191800-74192200	Enhancers	Duodenum Smooth Muscle	Duodenum
24	chr5:74191800-74192200	Enhancers	Ovary	ovary
25	chr5:74191800-74192200	Enhancers	Pancreas	Pancrea
26	chr5:74191800-74192200	Enhancers	NHEK	skin
27	chr5:74191800-74192400	Enhancers	Breast Myoepithelial Primary Cells	Breast
28	chr5:74191800-74192400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
29	chr5:74191800-74192400	Flanking Active TSS	Brain Anterior Caudate	brain
30	chr5:74191800-74192400	Flanking Active TSS	Brain Hippocampus Middle	brain
31	chr5:74191800-74192400	Enhancers	Osteobl	bone
32	chr5:74191800-74193000	Enhancers	Cortex derived primary cultured neurospheres	brain
33	chr5:74192000-74192200	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
34	chr5:74192000-74192200	Bivalent Enhancer	Duodenum Mucosa	Duodenum
35	chr5:74192000-74192400	Enhancers	Right Atrium	heart
36	chr5:74192000-74192400	Enhancers	Right Ventricle	heart
37	chr5:74192000-74193200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
38	chr5:74192000-74199000	Weak transcription	H9 Cell Line	embryonic stem cell
39	chr5:74192200-74192400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
40	chr5:74192400-74192800	Weak transcription	Osteobl	bone
41	chr5:74192800-74193200	Enhancers	Osteobl	bone
42	chr5:74193000-74193200	Enhancers	HUES6 Cell Line	embryonic stem cell
43	chr5:74193000-74193400	Flanking Active TSS	K562	blood
44	chr5:74193200-74197000	Weak transcription	HUES6 Cell Line	embryonic stem cell
45	chr5:74193400-74193800	Active TSS	K562	blood
46	chr5:74197000-74197200	Enhancers	HUES64 Cell Line	embryonic stem cell
47	chr5:74197000-74197400	Enhancers	ES-WA7 Cell Line	embryonic stem cell
48	chr5:74197000-74197600	Enhancers	HUES6 Cell Line	embryonic stem cell
49	chr5:74197200-74197400	Enhancers	ES-I3 Cell Line	embryonic stem cell
50	chr5:74197400-74199000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell

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