Variant report

Variant	nsv869260
Chromosome Location	chr7:140404835-140542905
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:140510896-140511233	HepG2	liver:	n/a	n/a
2	ARID3A	chr7:140441286-140441486	K562	blood:	n/a	n/a
3	ARID3A	chr7:140529728-140530047	HepG2	liver:	n/a	n/a
4	ARID3A	chr7:140510883-140511230	K562	blood:	n/a	n/a
5	ARID3A	chr7:140443757-140444069	HepG2	liver:	n/a	n/a
6	ARID3A	chr7:140424401-140424425	K562	blood:	n/a	n/a
7	ATF1	chr7:140510925-140511232	K562	blood:	n/a	n/a
8	BACH1	chr7:140508278-140508341	H1-hESC	embryonic stem cell:	n/a	n/a
9	BHLHE40	chr7:140510798-140511306	K562	blood:	n/a	n/a
10	BHLHE40	chr7:140541129-140541295	K562	blood:	n/a	n/a
11	BRCA1	chr7:140407525-140407543	Hela-S3	cervix:	n/a	n/a
12	CCNT2	chr7:140513572-140513613	K562	blood:	n/a	n/a
13	CEBPB	chr7:140452352-140452824	MCF-7	breast:	n/a	chr7:140452566-140452579 chr7:140452566-140452577
14	CEBPB	chr7:140407071-140407271	HepG2	liver:	n/a	chr7:140407200-140407211 chr7:140407201-140407210
15	CEBPB	chr7:140540050-140540115	K562	blood:	n/a	n/a
16	CEBPB	chr7:140469738-140469947	K562	blood:	n/a	n/a
17	CEBPB	chr7:140452370-140452718	A549	lung:	n/a	chr7:140452566-140452579 chr7:140452566-140452577
18	CEBPB	chr7:140449761-140450074	K562	blood:	n/a	chr7:140449899-140449912 chr7:140449899-140449912 chr7:140449901-140449910 chr7:140449901-140449912 chr7:140449901-140449910 chr7:140449899-140449910 chr7:140449901-140449910 chr7:140449901-140449910
19	CEBPB	chr7:140422119-140422389	HepG2	liver:	n/a	chr7:140422214-140422225
20	CEBPB	chr7:140541231-140541467	HepG2	liver:	n/a	chr7:140541336-140541347
21	CEBPB	chr7:140452069-140452762	HepG2	liver:	n/a	chr7:140452566-140452579 chr7:140452566-140452577
22	CEBPB	chr7:140452417-140452668	K562	blood:	n/a	chr7:140452566-140452579 chr7:140452566-140452577
23	CEBPB	chr7:140452362-140452751	ECC-1	luminal epithelium:	n/a	chr7:140452566-140452579 chr7:140452566-140452577
24	CEBPB	chr7:140469678-140469958	Hela-S3	cervix:	n/a	n/a
25	CEBPB	chr7:140541246-140541461	K562	blood:	n/a	chr7:140541336-140541347
26	CEBPB	chr7:140452373-140452748	MCF-7	breast:	n/a	chr7:140452566-140452579 chr7:140452566-140452577
27	CEBPB	chr7:140452473-140452652	HepG2	liver:	n/a	chr7:140452566-140452579 chr7:140452566-140452577
28	CEBPB	chr7:140422034-140422410	ECC-1	luminal epithelium:	n/a	chr7:140422214-140422225
29	CEBPB	chr7:140407166-140407288	Hela-S3	cervix:	n/a	chr7:140407200-140407211 chr7:140407201-140407210
30	CEBPB	chr7:140449718-140450079	HepG2	liver:	n/a	chr7:140449899-140449912 chr7:140449899-140449912 chr7:140449901-140449910 chr7:140449901-140449912 chr7:140449901-140449910 chr7:140449899-140449910 chr7:140449901-140449910 chr7:140449901-140449910
31	CEBPB	chr7:140472541-140472764	K562	blood:	n/a	chr7:140472602-140472615
32	CEBPB	chr7:140541229-140541416	A549	lung:	n/a	chr7:140541336-140541347
33	CEBPB	chr7:140428147-140428649	IMR90	lung:	n/a	chr7:140428533-140428550
34	CEBPB	chr7:140452286-140452756	A549	lung:	n/a	chr7:140452566-140452579 chr7:140452566-140452577
35	CEBPB	chr7:140541160-140541513	Hela-S3	cervix:	n/a	chr7:140541336-140541347
36	CEBPB	chr7:140452355-140452759	K562	blood:	n/a	chr7:140452566-140452579 chr7:140452566-140452577
37	CEBPB	chr7:140452392-140452752	Hela-S3	cervix:	n/a	chr7:140452566-140452579 chr7:140452566-140452577
38	CEBPB	chr7:140452379-140452752	IMR90	lung:	n/a	chr7:140452566-140452579 chr7:140452566-140452577
39	CEBPB	chr7:140449735-140450037	A549	lung:	n/a	chr7:140449899-140449912 chr7:140449899-140449912 chr7:140449901-140449910 chr7:140449901-140449912 chr7:140449901-140449910 chr7:140449899-140449910 chr7:140449901-140449910 chr7:140449901-140449910
40	CEBPB	chr7:140407043-140407355	K562	blood:	n/a	chr7:140407200-140407211 chr7:140407201-140407210
41	CEBPB	chr7:140422165-140422344	Hela-S3	cervix:	n/a	chr7:140422214-140422225
42	CEBPB	chr7:140452194-140452743	A549	lung:	n/a	chr7:140452566-140452579 chr7:140452566-140452577
43	CEBPB	chr7:140452370-140452755	ECC-1	luminal epithelium:	n/a	chr7:140452566-140452579 chr7:140452566-140452577
44	CEBPB	chr7:140522901-140523170	IMR90	lung:	n/a	n/a
45	CEBPB	chr7:140452434-140452680	HepG2	liver:	n/a	chr7:140452566-140452579 chr7:140452566-140452577
46	CEBPB	chr7:140469721-140469996	MCF-7	breast:	n/a	n/a
47	CEBPB	chr7:140406992-140407275	K562	blood:	n/a	chr7:140407200-140407211 chr7:140407201-140407210
48	CEBPB	chr7:140541174-140541505	IMR90	lung:	n/a	chr7:140541336-140541347
49	CEBPB	chr7:140483969-140484138	K562	blood:	n/a	n/a
50	CEBPB	chr7:140422048-140422367	IMR90	lung:	n/a	chr7:140422214-140422225

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:140452281-140452331	CMK	blood:	n/a
2	chr7:140454740-140454790	NHBE	bronchial:	n/a
3	chr7:140452281-140452331	HNPCEpiC	eye:	n/a
4	chr7:140452281-140452331	SK-N-SH_RA	brain:	n/a
5	chr7:140405191-140405241	GM12891	blood:	n/a
6	chr7:140405191-140405241	AG10803	skin:	n/a
7	chr7:140452281-140452331	HRPEpiC	eye:	n/a
8	chr7:140452281-140452331	SAEC	small airway:	n/a
9	chr7:140452281-140452331	Hela-S3	cervix:	n/a
10	chr7:140405191-140405241	AG09319	gingival:	n/a
11	chr7:140454740-140454790	AG09319	gingival:	n/a
12	chr7:140454740-140454790	NB4	blood:	n/a
13	chr7:140454740-140454790	AoSMC	blood vessel:	n/a
14	chr7:140405191-140405241	GM12878	blood:	n/a
15	chr7:140452281-140452331	AG09319	gingival:	n/a
16	chr7:140452281-140452331	HCT-116	colon:	n/a
17	chr7:140405191-140405241	H1-hESC	embryonic stem cell:	embryo
18	chr7:140452281-140452331	U87	brain:	n/a
19	chr7:140454740-140454790	HRCEpiC	kidney:	n/a
20	chr7:140405191-140405241	K562	blood:	n/a
21	chr7:140454740-140454790	GM12878	blood:	n/a
22	chr7:140405191-140405241	BJ	skin:	n/a
23	chr7:140454740-140454790	GM12891	blood:	n/a
24	chr7:140454740-140454790	HCM	heart:	n/a
25	chr7:140405191-140405241	PrEC	prostate:	n/a
26	chr7:140405191-140405241	AG04450	lung:	fetal
27	chr7:140405191-140405241	HCPEpiC	choroid plexus:	n/a
28	chr7:140454740-140454790	SK-N-MC	brain:	n/a
29	chr7:140405191-140405241	T-47D	breast:	n/a
30	chr7:140405191-140405241	NHDF-neo	bronchial:	n/a
31	chr7:140452281-140452331	HIPEpiC	eye:	n/a
32	chr7:140454740-140454790	ProgFib	skin:	n/a
33	chr7:140454740-140454790	IMR90	lung:	fetal
34	chr7:140454740-140454790	SK-N-SH	brain:	n/a
35	chr7:140452281-140452331	SKMC	muscle:	n/a
36	chr7:140405191-140405241	HL-60	blood:	n/a
37	chr7:140454740-140454790	MCF-7	breast:	n/a
38	chr7:140452281-140452331	HCF	heart:	n/a
39	chr7:140452281-140452331	NHDF-neo	bronchial:	n/a
40	chr7:140454740-140454790	GM12892	blood:	n/a
41	chr7:140452281-140452331	RPTEC	kidney:	n/a
42	chr7:140405191-140405241	HUVEC	blood vessel:	n/a
43	chr7:140454740-140454790	BJ	skin:	n/a
44	chr7:140452281-140452331	Hepatocyte	liver:	n/a
45	chr7:140452281-140452331	MCF-7	breast:	n/a
46	chr7:140405191-140405241	AoSMC	blood vessel:	n/a
47	chr7:140405191-140405241	Hela-S3	cervix:	n/a
48	chr7:140405191-140405241	PANC-1	pancreas:	n/a
49	chr7:140454740-140454790	HUVEC	blood vessel:	n/a
50	chr7:140454740-140454790	PrEC	prostate:	n/a

No.	Distal block	Cell Line	Cell type
1	chr7:140504577..140509209-chr7:140711163..140714577,4	MCF-7	breast:
2	chr7:140448573..140452334-chr7:140454838..140458113,4	K562	blood:
3	chr7:140397557..140400522-chr7:140416030..140418868,2	K562	blood:
4	chr7:140400483..140403338-chr7:140425369..140427117,2	K562	blood:
5	chr7:140396427..140399298-chr7:140424412..140427398,2	K562	blood:
6	chr7:140510400..140511598-chr7:140711292..140712616,8	MCF-7	breast:
7	chr7:140466871..140469366-chr7:140475800..140478111,2	K562	blood:
8	chr7:140509634..140513018-chr7:140622875..140626289,4	MCF-7	breast:
9	chr7:140402875..140405225-chr7:140478339..140480475,2	K562	blood:
10	chr7:140371233..140372859-chr7:140417535..140420248,2	MCF-7	breast:
11	chr7:140416340..140419154-chr7:140424735..140426861,2	MCF-7	breast:
12	chr7:140416340..140419154-chr7:140424735..140426861,2	MCF-7	breast:
13	chr7:140429621..140431191-chr7:140448921..140450687,2	K562	blood:
14	chr7:140458046..140459583-chr7:140475705..140477212,2	K562	blood:
15	chr7:140510589..140511483-chr7:141349656..141350638,2	K562	blood:
16	chr7:140477323..140479945-chr7:140493783..140496200,2	K562	blood:
17	chr7:140478118..140480859-chr7:140482682..140485290,2	MCF-7	breast:
18	chr7:140500393..140502235-chr7:140644520..140646531,2	K562	blood:
19	chr7:140443740..140445240-chr7:140449142..140451877,2	MCF-7	breast:
20	chr7:140423472..140425930-chr7:140432737..140435210,2	K562	blood:
21	chr7:140540956..140543931-chr7:140548791..140552881,3	MCF-7	breast:
22	chr7:140425976..140426774-chr7:140510803..140511321,2	MCF-7	breast:
23	chr7:140414826..140417394-chr7:140419160..140421169,2	K562	blood:
24	chr7:140478967..140482699-chr7:140484406..140488257,5	K562	blood:
25	chr7:140434733..140440913-chr7:140443989..140447709,5	K562	blood:
26	chr7:140485728..140487377-chr7:140491340..140494187,2	K562	blood:
27	chr7:140486692..140490040-chr7:140490086..140493321,3	K562	blood:
28	chr7:140471384..140473215-chr7:140476051..140478327,3	K562	blood:
29	chr7:140530086..140533058-chr7:140712020..140715730,3	K562	blood:
30	chr7:140372677..140375381-chr7:140516838..140518522,2	MCF-7	breast:
31	chr7:140510609..140511544-chr7:140920071..140920742,2	MCF-7	breast:
32	chr7:140505697..140508092-chr7:140511618..140514170,3	K562	blood:
33	chr7:140448573..140452334-chr7:140454838..140458113,4	K562	blood:
34	chr7:140536159..140538632-chr7:140712528..140714752,3	MCF-7	breast:
35	chr7:140447067..140448647-chr7:140714489..140716015,2	MCF-7	breast:
36	chr7:140486692..140490040-chr7:140490086..140493321,3	K562	blood:
37	chr7:140421606..140424129-chr7:140426224..140428173,2	MCF-7	breast:
38	chr7:140508977..140512218-chr7:140712062..140714684,5	MCF-7	breast:
39	chr7:140402003..140403554-chr7:140431273..140432954,2	MCF-7	breast:
40	chr7:140425846..140426811-chr7:140711662..140712678,3	MCF-7	breast:
41	chr7:140424087..140425930-chr7:140432654..140434237,2	K562	blood:
42	chr7:140541066..140543688-chr7:140623190..140625877,3	K562	blood:
43	chr7:140425976..140426774-chr7:140510803..140511321,2	MCF-7	breast:
44	chr7:140509026..140511710-chr7:140712128..140713632,2	K562	blood:
45	chr7:140414826..140417259-chr7:140419669..140421264,2	K562	blood:
46	chr7:140508535..140511322-chr7:140704600..140707127,2	MCF-7	breast:
47	chr7:140443946..140445790-chr7:140457847..140460570,2	K562	blood:
48	chr7:140485728..140487377-chr7:140491340..140494187,2	K562	blood:
49	chr7:140371637..140374196-chr7:140414800..140417349,2	MCF-7	breast:
50	chr7:140429621..140431191-chr7:140448921..140450687,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-BRAF-1	chr7:140425329-140426316	NONHSAT123693
2	lnc-BRAF-1	chr7:140419593-140421126	NONHSAT123693
3	lnc-BRAF-1	chr7:140422072-140423908	NONHSAT123693
4	lnc-BRAF-1	chr7:140419138-140421887	NONHSAT123692
5	lnc-BRAF-1	chr7:140419138-140421228	NONHSAT123691

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	NDUFB2	hsa-miR-19b-3p	chr7:140406384-140406406

Variant related genes	Relation type
BRAF	TF binding region
BRAF	CpG island
ENSG00000240889	chromatin interactions
ENSG00000090266	chromatin interactions
ENSG00000090263	chromatin interactions
ENSG00000146966	chromatin interactions
ENSG00000273081	chromatin interactions
ENSG00000157764	chromatin interactions
ENSG00000133597	chromatin interactions

Extended variants
information (count: 4894 )
Associated
traits (count: 98 )

Variant overlapped rSNPs/rCNVs (count:4894 , 50 per page) page: 1 2 3 4 5 6 7 ... 98

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs59579457	chr7:140404850-140404851	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs551065668	chr7:140404924-140404925	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs563265311	chr7:140404938-140404939	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs186561084	chr7:140404942-140404943	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs549256255	chr7:140404953-140404954	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs567517091	chr7:140404960-140404961	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs563436225	chr7:140404961-140404962	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs534803485	chr7:140404967-140404968	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs377660766	chr7:140405040-140405041	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs547152650	chr7:140405062-140405063	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs530846476	chr7:140405102-140405103	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs368987534	chr7:140405120-140405121	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs537407079	chr7:140405221-140405222	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs190539051	chr7:140405222-140405223	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs117865960	chr7:140405234-140405235	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs536548380	chr7:140405356-140405357	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs116590115	chr7:140405430-140405431	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs573141398	chr7:140405431-140405432	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs181848344	chr7:140405438-140405439	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs559000797	chr7:140405517-140405518	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs577685327	chr7:140405534-140405535	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs2364396	chr7:140405560-140405561	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
23	rs563145244	chr7:140405655-140405656	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs186447748	chr7:140405674-140405675	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs2364397	chr7:140405706-140405707	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
26	rs561152662	chr7:140405720-140405721	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs528325377	chr7:140405754-140405755	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs546839906	chr7:140405798-140405799	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs572869632	chr7:140405802-140405803	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs568551749	chr7:140405824-140405825	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs374708869	chr7:140405829-140405830	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs202028313	chr7:140405831-140405832	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs4020754	chr7:140405856-140405857	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs4020755	chr7:140405858-140405859	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs371154203	chr7:140405859-140405860	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs4020756	chr7:140405860-140405861	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs71522109	chr7:140405862-140405863	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs571387026	chr7:140405863-140405864	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs538766242	chr7:140405865-140405866	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs111930895	chr7:140405878-140405879	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs74407883	chr7:140405909-140405910	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs72356654	chr7:140405910-140405911	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs370976890	chr7:140405938-140405939	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs373737360	chr7:140405952-140405953	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs146143972	chr7:140405988-140405989	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs569201508	chr7:140406055-140406056	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs9691722	chr7:140406139-140406140	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs554875131	chr7:140406173-140406174	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs367611495	chr7:140406267-140406268	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs77681991	chr7:140406288-140406289	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:98)

Disease	PMID	Source
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Thyroid cancer	19087340	CNVD
Seminomas	18059402	CNVD
Testicular cancer	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	19415332	CNVD
Medulloblastoma	21979893	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
T-cell lymphomas	19863542	CNVD
Malaria	21533027	CNVD
Melanoma	18172304	CNVD
Renal cell carcinoma	19461508	CNVD
head and neck squamous cell carcinoma	19289630	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Wilms tumour	21544195	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Squamous cell cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Astrocytoma	17387387	CNVD
Glioblastoma multiforme	17387387	CNVD
Low-grade fibromyxoid sarcoma	0	CNVD
Oligodendroglial tumors	17285580	CNVD
Endometrial cancer	22040021	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	21264507	CNVD
Shwachman-Diamond syndrome	22934832	CNVD
Colorectal cancer	19359472	CNVD
Cutaneous malignant melanoma	17690212	CNVD
Leukemia	17361228	CNVD
Breast cancer	16461572	CNVD
Peripheral t-cell lymphoma	19118030	CNVD
Malignant melanoma	17690212	CNVD
Renal cell carcinoma	18592004	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Multiple myeloma	17550852	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Neurodevelopmental disorder	22521361	CNVD
abortions and stillbirths	19751515	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Acute myeloid leukemia	20729466	CNVD
Lung cancer	18438408	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Burkitt''s lymphoma	19759907	CNVD
Chronic myeloid leukemia	21384125	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
lymphocytic leukemia	21291569	CNVD
Acute myeloid leukemia	21251322	CNVD
Prostate cancer	16573809	CNVD
Medulloblastoma	16783165	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Melanoma	19188590	CNVD
Glioblastoma multiforme	18628472	CNVD
abnormal development	18461090	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Malignant melanoma	17260012	CNVD
Coffin-Siris syndrome	21572526	CNVD
Papillary thyroid carcinoma	21436994	CNVD
small cell lung cancer	20016488	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Hodgkin''s lymphoma	18179710	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Breast cancer	16272173	CNVD
Myxofibrosarcoma	16751306	CNVD
Stuttering	21108403	CNVD
Breast cancer	17603634	CNVD
Urothelial carcinoma	18382360	CNVD
Myelodysplastic syndrome	17634407	CNVD
Cancer	21129771	CNVD
Myelofibrosis	22110671	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
T-cell acute lymphoblastic leukemia	16673021	CNVD
Cancer	21183584	CNVD
Intracranial ependymoma	16609018	CNVD
Non-small cell lung cancer	21829676	CNVD
Developmental delay	19490664	CNVD
Pancreatitis	20877625	CNVD
Multiple myeloma	16461302	CNVD
Neuroblastoma	18923191	CNVD
Low-grade astrocytoma	19016743	CNVD
Medulloblastoma	16968546	CNVD
Pilocytic astrocytoma	18408760	CNVD
Idiopathic chronic pancreatitis	19584086	CNVD
Pediatric low-grade astrocytoma	19016743	CNVD
Acute lymphoblastic leukemia	17315016	CNVD
Gastric cancer	16891809	CNVD
Cancer	17440070	CNVD
Astrocytoma	18398503	CNVD
Melanoma	19671679	CNVD
Lung adenocarcinoma	19525976	CNVD
Lung cancer	19525976	CNVD
Breast cancer	17133270	CNVD
Schizophrenia	17646849	CNVD
Glioblastoma multiforme	21525872	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:2522 , 50 per page) page: 1 2 3 4 5 6 7 ... 51

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:140397600-140407400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
2	chr7:140397800-140405800	Weak transcription	Aorta	Aorta
3	chr7:140397800-140406800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr7:140398000-140406000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
5	chr7:140398000-140406800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
6	chr7:140398000-140408800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
7	chr7:140398000-140419400	Weak transcription	Primary neutrophils fromperipheralblood	blood
8	chr7:140398000-140466600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
9	chr7:140398200-140406000	Weak transcription	Fetal Lung	lung
10	chr7:140398200-140406000	Weak transcription	HSMM	muscle
11	chr7:140398200-140473800	Weak transcription	Rectal Smooth Muscle	rectum
12	chr7:140398200-140492600	Weak transcription	Colonic Mucosa	Colon
13	chr7:140398400-140405400	Weak transcription	Muscle Satellite Cultured Cells	--
14	chr7:140398400-140405800	Weak transcription	Fetal Kidney	kidney
15	chr7:140398400-140406000	Weak transcription	Stomach Mucosa	stomach
16	chr7:140398400-140408400	Weak transcription	NHDF-Ad	bronchial
17	chr7:140398400-140422000	Weak transcription	Pancreatic Islets	Pancreatic Islet
18	chr7:140398400-140432200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
19	chr7:140398600-140405400	Weak transcription	NH-A	brain
20	chr7:140398600-140414800	Weak transcription	Small Intestine	intestine
21	chr7:140398600-140459400	Weak transcription	Brain Germinal Matrix	brain
22	chr7:140398600-140491800	Weak transcription	Fetal Brain Male	brain
23	chr7:140399400-140405400	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
24	chr7:140399400-140407000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
25	chr7:140399400-140414200	Weak transcription	Gastric	stomach
26	chr7:140399400-140468200	Weak transcription	Right Ventricle	heart
27	chr7:140399600-140408000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
28	chr7:140399600-140443800	Weak transcription	Fetal Heart	heart
29	chr7:140400000-140474000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
30	chr7:140401200-140407000	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
31	chr7:140402200-140405000	Strong transcription	Cortex derived primary cultured neurospheres	brain
32	chr7:140402200-140407200	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
33	chr7:140402200-140407200	Strong transcription	Primary T cells from cord blood	blood
34	chr7:140402200-140407200	Strong transcription	Primary T helper cells fromperipheralblood	blood
35	chr7:140402400-140405200	Strong transcription	Rectal Mucosa Donor 31	rectum
36	chr7:140402400-140407000	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
37	chr7:140402400-140407200	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
38	chr7:140402400-140407200	Strong transcription	Duodenum Mucosa	Duodenum
39	chr7:140402400-140408200	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
40	chr7:140402600-140405000	Strong transcription	Foreskin Fibroblast Primary Cells skin02	Skin
41	chr7:140402600-140405200	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
42	chr7:140402600-140406600	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
43	chr7:140402600-140406800	Strong transcription	Liver	Liver
44	chr7:140402600-140407200	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
45	chr7:140402600-140407200	Strong transcription	HUES6 Cell Line	embryonic stem cell
46	chr7:140402600-140407200	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
47	chr7:140402600-140407200	Strong transcription	Primary hematopoietic stem cells short term culture	blood
48	chr7:140402600-140407200	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
49	chr7:140402600-140407200	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
50	chr7:140402600-140407200	Strong transcription	Fetal Adrenal Gland	Adrenal Gland

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