Variant report

Variant	nsv1018865
Chromosome Location	chr5:74246293-74494552
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2064)
CpG islands
(count:1708)
Chromatin interactive
region (count:53)
LncRNA
region (count:20)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2064 , 50 per page) page: 1 2 3 4 5 6 7 ... 42

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr5:74250044-74251228	HepG2	liver:	n/a	n/a
2	ARID3A	chr5:74391290-74391528	HepG2	liver:	n/a	n/a
3	ARID3A	chr5:74306723-74307157	HepG2	liver:	n/a	n/a
4	ARID3A	chr5:74485211-74485511	HepG2	liver:	n/a	n/a
5	ARID3A	chr5:74293577-74293804	HepG2	liver:	n/a	n/a
6	ARID3A	chr5:74333093-74333098	HepG2	liver:	n/a	n/a
7	ARID3A	chr5:74463323-74463328	HepG2	liver:	n/a	n/a
8	ATF2	chr5:74349551-74350155	H1-hESC	embryonic stem cell:	n/a	n/a
9	ATF2	chr5:74344241-74344923	GM12878	blood:	n/a	n/a
10	ATF2	chr5:74351364-74352195	H1-hESC	embryonic stem cell:	n/a	n/a
11	ATF2	chr5:74345596-74346055	H1-hESC	embryonic stem cell:	n/a	n/a
12	ATF2	chr5:74382845-74383273	GM12878	blood:	n/a	n/a
13	ATF3	chr5:74391161-74391637	HCT-116	colon:	n/a	n/a
14	BACH1	chr5:74493585-74493943	K562	blood:	n/a	n/a
15	BACH1	chr5:74493604-74493975	H1-hESC	embryonic stem cell:	n/a	n/a
16	BACH1	chr5:74346230-74346497	H1-hESC	embryonic stem cell:	n/a	n/a
17	BACH1	chr5:74348686-74350492	H1-hESC	embryonic stem cell:	n/a	n/a
18	BATF	chr5:74344236-74344915	GM12878	blood:	n/a	n/a
19	BATF	chr5:74340153-74340494	GM12878	blood:	n/a	chr5:74340315-74340326
20	BATF	chr5:74344363-74344864	GM12878	blood:	n/a	n/a
21	BATF	chr5:74382934-74383265	GM12878	blood:	n/a	chr5:74383066-74383077
22	BATF	chr5:74382894-74383194	GM12878	blood:	n/a	chr5:74383066-74383077
23	BATF	chr5:74340186-74340495	GM12878	blood:	n/a	chr5:74340315-74340326
24	BCL11A	chr5:74382987-74383167	GM12878	blood:	n/a	n/a
25	BCL11A	chr5:74330662-74330978	GM12878	blood:	n/a	n/a
26	BCL11A	chr5:74382912-74383310	GM12878	blood:	n/a	n/a
27	BCL3	chr5:74382922-74383260	GM12878	blood:	n/a	n/a
28	BCL3	chr5:74312708-74313047	GM12878	blood:	n/a	n/a
29	BCL3	chr5:74442051-74442314	GM12878	blood:	n/a	n/a
30	BCL3	chr5:74312620-74313128	GM12878	blood:	n/a	n/a
31	BCL3	chr5:74382964-74383215	GM12878	blood:	n/a	n/a
32	BHLHE40	chr5:74344153-74344917	GM12878	blood:	n/a	n/a
33	BHLHE40	chr5:74349196-74349715	HepG2	liver:	n/a	chr5:74349390-74349406 chr5:74349377-74349393 chr5:74349389-74349405
34	BHLHE40	chr5:74361423-74361553	HepG2	liver:	n/a	n/a
35	BHLHE40	chr5:74317260-74317368	K562	blood:	n/a	n/a
36	BHLHE40	chr5:74250138-74250843	HepG2	liver:	n/a	n/a
37	BRCA1	chr5:74248648-74248659	GM12878	blood:	n/a	n/a
38	BRCA1	chr5:74391238-74391645	Hela-S3	cervix:	n/a	n/a
39	BRCA1	chr5:74407638-74408236	Hela-S3	cervix:	n/a	n/a
40	BRCA1	chr5:74349979-74350422	H1-hESC	embryonic stem cell:	n/a	n/a
41	BRCA1	chr5:74348656-74348704	HepG2	liver:	n/a	n/a
42	BRCA1	chr5:74349319-74349422	HepG2	liver:	n/a	n/a
43	BRCA1	chr5:74409126-74409996	Hela-S3	cervix:	n/a	n/a
44	BRCA1	chr5:74387620-74387635	GM12878	blood:	n/a	n/a
45	CBX3	chr5:74332829-74333508	HCT-116	colon:	n/a	n/a
46	CBX3	chr5:74463153-74463586	HCT-116	colon:	n/a	n/a
47	CBX3	chr5:74457355-74457583	K562	blood:	n/a	n/a
48	CBX3	chr5:74340035-74340699	HCT-116	colon:	n/a	n/a
49	CBX3	chr5:74332824-74333456	HCT-116	colon:	n/a	n/a
50	CCNT2	chr5:74493718-74493858	K562	blood:	n/a	n/a

(count:1708 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:74347539-74347589	AoSMC	blood vessel:	n/a
2	chr5:74346260-74346310	NH-A	brain:	n/a
3	chr5:74303397-74303447	ProgFib	skin:	n/a
4	chr5:74347539-74347589	PFSK-1	brain:	n/a
5	chr5:74326281-74326331	HRPEpiC	eye:	n/a
6	chr5:74353010-74353060	HUVEC	blood vessel:	n/a
7	chr5:74438852-74438902	GM12892	blood:	n/a
8	chr5:74330737-74330787	NHDF-neo	bronchial:	n/a
9	chr5:74348187-74348237	GM12892	blood:	n/a
10	chr5:74348187-74348237	HL-60	blood:	n/a
11	chr5:74347539-74347589	Jurkat	blood:	n/a
12	chr5:74349804-74349854	GM06990	blood:	n/a
13	chr5:74438852-74438902	SK-N-SH	brain:	n/a
14	chr5:74344416-74344466	NB4	blood:	n/a
15	chr5:74350815-74350865	Caco-2	colon:	n/a
16	chr5:74303397-74303447	AG04450	lung:	fetal
17	chr5:74344416-74344466	HCT-116	colon:	n/a
18	chr5:74330425-74330475	AG09309	skin:	n/a
19	chr5:74346260-74346310	GM12892	blood:	n/a
20	chr5:74328211-74328261	LNCaP	prostate:	n/a
21	chr5:74350214-74350264	Jurkat	blood:	n/a
22	chr5:74348373-74348423	HNPCEpiC	eye:	n/a
23	chr5:74328211-74328261	HCPEpiC	choroid plexus:	n/a
24	chr5:74330737-74330787	AG10803	skin:	n/a
25	chr5:74327277-74327327	A549	lung:	n/a
26	chr5:74348373-74348423	IMR90	lung:	fetal
27	chr5:74330425-74330475	NHDF-neo	bronchial:	n/a
28	chr5:74327277-74327327	IMR90	lung:	fetal
29	chr5:74348903-74348953	ProgFib	skin:	n/a
30	chr5:74348373-74348423	K562	blood:	n/a
31	chr5:74349644-74349694	HCPEpiC	choroid plexus:	n/a
32	chr5:74330737-74330787	GM12891	blood:	n/a
33	chr5:74346260-74346310	HRE	kidney:	n/a
34	chr5:74354835-74354885	Hepatocyte	liver:	n/a
35	chr5:74327281-74327331	NB4	blood:	n/a
36	chr5:74327277-74327327	NB4	blood:	n/a
37	chr5:74346260-74346310	HMEC	breast:	n/a
38	chr5:74350132-74350182	AG09309	skin:	n/a
39	chr5:74346260-74346310	AoSMC	blood vessel:	n/a
40	chr5:74327277-74327327	HIPEpiC	eye:	n/a
41	chr5:74350214-74350264	NH-A	brain:	n/a
42	chr5:74349993-74350043	HUVEC	blood vessel:	n/a
43	chr5:74333288-74333338	BJ	skin:	n/a
44	chr5:74349804-74349854	SK-N-SH_RA	brain:	n/a
45	chr5:74348373-74348423	AG09309	skin:	n/a
46	chr5:74327281-74327331	PFSK-1	brain:	n/a
47	chr5:74349993-74350043	NH-A	brain:	n/a
48	chr5:74350214-74350264	A549	lung:	n/a
49	chr5:74326281-74326331	GM12878	blood:	n/a
50	chr5:74344779-74344829	A549	lung:	n/a

(count:53 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr5:74245711..74248702-chr5:74259908..74262070,2	MCF-7	breast:
2	chr5:74318809..74320982-chr5:74323765..74325406,2	MCF-7	breast:
3	chr5:74334981..74336782-chr5:74342190..74344248,2	MCF-7	breast:
4	chr5:74245978..74248569-chr5:74531357..74534080,2	MCF-7	breast:
5	chr5:74315848..74318238-chr5:74328353..74330042,2	MCF-7	breast:
6	chr5:74265415..74267966-chr5:74268550..74270837,2	K562	blood:
7	chr5:74331704..74333232-chr5:74343101..74344687,2	MCF-7	breast:
8	chr5:74398898..74401626-chr5:74404084..74405845,2	K562	blood:
9	chr5:74481183..74484880-chr5:74486837..74490307,3	K562	blood:
10	chr5:74245711..74248702-chr5:74259908..74262070,2	MCF-7	breast:
11	chr5:74398898..74401626-chr5:74404084..74405845,2	K562	blood:
12	chr5:74459995..74462741-chr5:74463456..74465776,2	K562	blood:
13	chr5:74265415..74267966-chr5:74268550..74270837,2	K562	blood:
14	chr5:74346800..74348616-chr5:74350730..74353345,2	MCF-7	breast:
15	chr5:74338841..74341157-chr5:74343981..74347541,4	MCF-7	breast:
16	chr5:74331704..74333232-chr5:74343101..74344687,2	MCF-7	breast:
17	chr5:74341045..74343910-chr5:74344011..74347485,4	MCF-7	breast:
18	chr5:74266271..74268697-chr5:74331711..74333363,2	MCF-7	breast:
19	chr5:74379971..74382375-chr5:74387089..74390026,2	K562	blood:
20	chr5:74349068..74351249-chr5:74356524..74358401,2	MCF-7	breast:
21	chr5:74315578..74317119-chr5:74341476..74343130,2	MCF-7	breast:
22	chr5:74330454..74335475-chr5:74336350..74340630,5	MCF-7	breast:
23	chr5:74343721..74346711-chr5:74348510..74350046,2	MCF-7	breast:
24	chr5:74315848..74318238-chr5:74328353..74330042,2	MCF-7	breast:
25	chr5:74341045..74343910-chr5:74344011..74347485,4	MCF-7	breast:
26	chr5:74379971..74382375-chr5:74387089..74390026,2	K562	blood:
27	chr5:73980015..73981765-chr5:74329525..74332329,2	MCF-7	breast:
28	chr5:74251721..74254234-chr5:74259787..74261989,3	MCF-7	breast:
29	chr5:74490335..74492474-chr5:74495385..74497140,2	K562	blood:
30	chr5:74332922..74335648-chr5:74338677..74341293,2	MCF-7	breast:
31	chr5:74409705..74412287-chr5:74414282..74416485,2	K562	blood:
32	chr5:74348653..74349615-chr5:74462874..74463564,2	MCF-7	breast:
33	chr5:74315578..74317119-chr5:74341476..74343130,2	MCF-7	breast:
34	chr5:74332922..74335648-chr5:74338677..74341293,2	MCF-7	breast:
35	chr5:74230526..74231383-chr5:74345361..74346008,2	MCF-7	breast:
36	chr11:57561542..57564393-chr5:74329604..74332106,2	MCF-7	breast:
37	chr5:74334981..74336782-chr5:74342190..74344248,2	MCF-7	breast:
38	chr5:74343645..74345260-chr5:74345382..74347449,2	K562	blood:
39	chr5:74349473..74351177-chr5:74531614..74533984,2	MCF-7	breast:
40	chr5:74481183..74484880-chr5:74486837..74490307,3	K562	blood:
41	chr5:74345728..74346291-chr5:74523458..74524224,2	MCF-7	breast:
42	chr5:74338841..74341157-chr5:74343981..74347541,4	MCF-7	breast:
43	chr5:74409705..74412287-chr5:74414282..74416485,2	K562	blood:
44	chr5:74251721..74254234-chr5:74259787..74261989,3	MCF-7	breast:
45	chr5:74345325..74346339-chr5:74561197..74562160,5	MCF-7	breast:
46	chr5:74491047..74493376-chr5:74495534..74497598,2	K562	blood:
47	chr15:87299754..87300537-chr5:74333585..74334466,2	MCF-7	breast:
48	chr5:74220860..74221763-chr5:74345733..74346235,2	MCF-7	breast:
49	chr5:74349068..74351249-chr5:74356524..74358401,2	MCF-7	breast:
50	chr5:74266271..74268697-chr5:74331711..74333363,2	MCF-7	breast:

(count:20 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ANKRD31-1	chr5:74343858-74343862	ENSG00000250889
2	lnc-GCNT4-1	chr5:74313254-74313367	ENSG00000249856.1
3	lnc-ANKRD31-1	chr5:74347994-74348052	ENSG00000250889
4	lnc-GCNT4-2	chr5:74339379-74339914	NONHSAT102193
5	lnc-NSA2-1	chr5:74271426-74271554	NONHSAT102189
6	lnc-NSA2-1	chr5:74271427-74271554	XLOC_004430
7	lnc-ANKRD31-1	chr5:74343858-74343862	XLOC_004890
8	lnc-ANKRD31-1	chr5:74343722-74343862	NONHSAT102195
9	lnc-ANKRD31-1	chr5:74349340-74349594	NONHSAT102195
10	lnc-GCNT4-2	chr5:74340718-74341142	NONHSAT102193
11	lnc-NSA2-8	chr5:74279794-74279971	l_2947_chr5:74279793-74307259_76bGuttman_hLF
12	lnc-GCNT4-2	chr5:74337995-74338722	NONHSAT102193
13	lnc-ANKRD31-1	chr5:74348254-74348668	ENSG00000250889
14	lnc-ANKRD31-1	chr5:74347993-74348052	XLOC_004890
15	lnc-NSA2-8	chr5:74307183-74307310	l_2947_chr5:74279793-74307259_76bGuttman_hLF
16	lnc-GCNT4-1	chr5:74283326-74283448	ENSG00000249856.1
17	lnc-GCNT4-3	chr5:74302538-74302837	NONHSAT102192
18	lnc-GCNT4-1	chr5:74319656-74319753	ENSG00000249856.1
19	lnc-ANKRD31-1	chr5:74348254-74348668	XLOC_004890
20	lnc-GCNT4-2	chr5:74337140-74337513	NONHSAT102193

No data

Variant related genes	Relation type
GCNT4	TF binding region
ENSG00000249157	TF binding region
RPL27AP5	TF binding region
ENSG00000250889	TF binding region
ANKRD31	TF binding region
ENSG00000249856	TF binding region
GCNT4	CpG island
ENSG00000249157	CpG island
RPL27AP5	CpG island
ENSG00000250889	CpG island
ANKRD31	CpG island
ENSG00000249856	CpG island
ENSG00000049860	chromatin interactions
ENSG00000249856	chromatin interactions
ENSG00000145700	chromatin interactions
ENSG00000250889	chromatin interactions
BCL2	miRNA target sites

Extended variants
information (count: 8034 )
Associated
traits (count: 92 )

Variant overlapped rSNPs/rCNVs (count:8034 , 50 per page) page: 1 2 3 4 5 6 7 ... 161

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs564601341	chr5:74246355-74246356	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs565811271	chr5:74246356-74246357	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs35595761	chr5:74246490-74246491	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs180695061	chr5:74246498-74246499	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs569930434	chr5:74246549-74246550	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs185949378	chr5:74246569-74246570	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs549251020	chr5:74246570-74246571	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs191155999	chr5:74246577-74246578	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs375295923	chr5:74246624-74246625	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs570100063	chr5:74246633-74246634	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs35036644	chr5:74246727-74246728	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs563951682	chr5:74246827-74246828	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs138393610	chr5:74246828-74246829	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs531254109	chr5:74246832-74246833	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs553494212	chr5:74246854-74246855	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs534894329	chr5:74246918-74246919	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs78404689	chr5:74246931-74246932	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs557892402	chr5:74246947-74246948	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs539177303	chr5:74246951-74246952	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs577959992	chr5:74246957-74246958	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs73124661	chr5:74247020-74247021	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs542078780	chr5:74247058-74247059	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs182874353	chr5:74247075-74247076	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs117099080	chr5:74247115-74247116	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs147646455	chr5:74247137-74247138	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs564332866	chr5:74247161-74247162	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs533431088	chr5:74247185-74247186	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs556152993	chr5:74247187-74247188	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs116205664	chr5:74247188-74247189	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs563477075	chr5:74247196-74247197	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs116737524	chr5:74247198-74247199	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs190363930	chr5:74247222-74247223	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs559574206	chr5:74247240-74247241	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs541775701	chr5:74247260-74247261	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs6875541	chr5:74247278-74247279	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs547337146	chr5:74247288-74247289	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs570378423	chr5:74247348-74247349	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs34668391	chr5:74247363-74247364	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs539444902	chr5:74247412-74247413	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs549885792	chr5:74247431-74247432	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs561770154	chr5:74247438-74247439	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs149118588	chr5:74247452-74247453	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs73124662	chr5:74247646-74247647	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs555604043	chr5:74247685-74247686	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs572263407	chr5:74247771-74247772	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs73124663	chr5:74247823-74247824	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs558104208	chr5:74247832-74247833	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs182913690	chr5:74247833-74247834	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs543452764	chr5:74247837-74247838	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs563438827	chr5:74247838-74247839	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:92)

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
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Breast cancer	22522925	CNVD
Melanoma	20877625	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:2347 , 50 per page) page: 1 2 3 4 5 6 7 ... 47

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:74241600-74248000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
2	chr5:74243600-74247400	Enhancers	Osteobl	bone
3	chr5:74244000-74246400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
4	chr5:74244200-74253400	Weak transcription	Aorta	Aorta
5	chr5:74244400-74247400	Weak transcription	Small Intestine	intestine
6	chr5:74244400-74249400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
7	chr5:74244400-74249800	Weak transcription	Ovary	ovary
8	chr5:74244400-74249800	Weak transcription	HSMM	muscle
9	chr5:74244600-74247800	Weak transcription	Pancreas	Pancrea
10	chr5:74244600-74248400	Weak transcription	Placenta	Placenta
11	chr5:74244600-74249800	Weak transcription	Gastric	stomach
12	chr5:74244600-74249800	Weak transcription	Spleen	Spleen
13	chr5:74244600-74250000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
14	chr5:74244600-74251600	Enhancers	NHLF	lung
15	chr5:74244800-74247800	Weak transcription	Fetal Stomach	stomach
16	chr5:74245000-74246400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
17	chr5:74245200-74248400	Weak transcription	Fetal Lung	lung
18	chr5:74245400-74247000	Enhancers	NH-A	brain
19	chr5:74245400-74256000	Enhancers	Fetal Intestine Large	intestine
20	chr5:74245600-74246400	Flanking Active TSS	NHDF-Ad	bronchial
21	chr5:74245600-74249600	Weak transcription	Liver	Liver
22	chr5:74245800-74246400	Enhancers	Primary hematopoietic stem cells short term culture	blood
23	chr5:74245800-74249000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
24	chr5:74245800-74249400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
25	chr5:74245800-74255800	Enhancers	Stomach Mucosa	stomach
26	chr5:74246000-74247000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
27	chr5:74246000-74247600	Weak transcription	Fetal Kidney	kidney
28	chr5:74246000-74249600	Weak transcription	Duodenum Mucosa	Duodenum
29	chr5:74246000-74249800	Weak transcription	Muscle Satellite Cultured Cells	--
30	chr5:74246200-74246400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
31	chr5:74246200-74246600	Weak transcription	Fetal Intestine Small	intestine
32	chr5:74246200-74246600	Weak transcription	HepG2	liver
33	chr5:74246200-74247000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
34	chr5:74246200-74248600	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
35	chr5:74246200-74249800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
36	chr5:74246200-74251600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
37	chr5:74246200-74259200	Weak transcription	Pancreatic Islets	Pancreatic Islet
38	chr5:74246400-74249600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
39	chr5:74246400-74249800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
40	chr5:74246400-74252000	Enhancers	NHDF-Ad	bronchial
41	chr5:74246600-74255000	Enhancers	HepG2	liver
42	chr5:74246600-74256600	Enhancers	Fetal Intestine Small	intestine
43	chr5:74247000-74247800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
44	chr5:74247000-74249400	Weak transcription	NH-A	brain
45	chr5:74247000-74253000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
46	chr5:74247400-74247600	Enhancers	Small Intestine	intestine
47	chr5:74247400-74249600	Weak transcription	Osteobl	bone
48	chr5:74247600-74248000	Weak transcription	Small Intestine	intestine
49	chr5:74247600-74250800	Enhancers	Fetal Kidney	kidney
50	chr5:74247800-74248600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived

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