Variant report

Variant	nsv427802
Chromosome Location	chr7:120749159-120935856
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1414)
CpG islands
(count:244)
Chromatin interactive
region (count:168)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1414 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:120918377-120919048	K562	blood:	n/a	n/a
2	ARID3A	chr7:120927612-120927751	K562	blood:	n/a	n/a
3	ARID3A	chr7:120800023-120800487	K562	blood:	n/a	n/a
4	ARID3A	chr7:120889642-120889728	K562	blood:	n/a	n/a
5	ARID3A	chr7:120778432-120778625	K562	blood:	n/a	n/a
6	ATF1	chr7:120918481-120919023	K562	blood:	n/a	n/a
7	ATF1	chr7:120778322-120778731	K562	blood:	n/a	n/a
8	ATF1	chr7:120799677-120800576	K562	blood:	n/a	n/a
9	ATF2	chr7:120918387-120919501	GM12878	blood:	n/a	n/a
10	ATF2	chr7:120820349-120820987	GM12878	blood:	n/a	n/a
11	ATF2	chr7:120820324-120820939	GM12878	blood:	n/a	n/a
12	ATF2	chr7:120778277-120778721	GM12878	blood:	n/a	n/a
13	ATF2	chr7:120918303-120919570	GM12878	blood:	n/a	n/a
14	ATF2	chr7:120778230-120778840	GM12878	blood:	n/a	n/a
15	ATF3	chr7:120778265-120778713	K562	blood:	n/a	n/a
16	ATF3	chr7:120918333-120919103	K562	blood:	n/a	n/a
17	ATF3	chr7:120800134-120800510	K562	blood:	n/a	n/a
18	BACH1	chr7:120808205-120808275	H1-hESC	embryonic stem cell:	n/a	n/a
19	BACH1	chr7:120779259-120779282	K562	blood:	n/a	n/a
20	BACH1	chr7:120830804-120830897	K562	blood:	n/a	n/a
21	BACH1	chr7:120869574-120869602	K562	blood:	n/a	n/a
22	BACH1	chr7:120918605-120919146	K562	blood:	n/a	n/a
23	BACH1	chr7:120771434-120771460	K562	blood:	n/a	n/a
24	BATF	chr7:120918321-120919159	GM12878	blood:	n/a	n/a
25	BATF	chr7:120912071-120912364	GM12878	blood:	n/a	chr7:120912190-120912201
26	BATF	chr7:120912001-120912317	GM12878	blood:	n/a	chr7:120912190-120912201
27	BATF	chr7:120820490-120820786	GM12878	blood:	n/a	n/a
28	BATF	chr7:120918686-120919199	GM12878	blood:	n/a	n/a
29	BCL11A	chr7:120918441-120919239	GM12878	blood:	n/a	n/a
30	BCL11A	chr7:120820486-120820825	GM12878	blood:	n/a	n/a
31	BCL11A	chr7:120918711-120919133	GM12878	blood:	n/a	n/a
32	BCL3	chr7:120820455-120820804	GM12878	blood:	n/a	n/a
33	BCL3	chr7:120918738-120919171	GM12878	blood:	n/a	n/a
34	BCLAF1	chr7:120820473-120821033	GM12878	blood:	n/a	n/a
35	BCLAF1	chr7:120918697-120919169	GM12878	blood:	n/a	n/a
36	BCLAF1	chr7:120918588-120919282	GM12878	blood:	n/a	n/a
37	BHLHE40	chr7:120777877-120777906	K562	blood:	n/a	n/a
38	BHLHE40	chr7:120800243-120800443	K562	blood:	n/a	n/a
39	BHLHE40	chr7:120851610-120851680	K562	blood:	n/a	n/a
40	BHLHE40	chr7:120820459-120820914	GM12878	blood:	n/a	n/a
41	BHLHE40	chr7:120778337-120778832	GM12878	blood:	n/a	n/a
42	BHLHE40	chr7:120918488-120918877	K562	blood:	n/a	n/a
43	BHLHE40	chr7:120918625-120919615	GM12878	blood:	n/a	n/a
44	BHLHE40	chr7:120778436-120778667	K562	blood:	n/a	n/a
45	BRCA1	chr7:120763041-120763396	Hela-S3	cervix:	n/a	n/a
46	BRCA1	chr7:120766937-120767255	Hela-S3	cervix:	n/a	n/a
47	BRCA1	chr7:120760594-120761193	Hela-S3	cervix:	n/a	n/a
48	BRCA1	chr7:120916258-120916947	Hela-S3	cervix:	n/a	n/a
49	BRCA1	chr7:120844643-120844790	Hela-S3	cervix:	n/a	n/a
50	BRCA1	chr7:120900492-120900623	Hela-S3	cervix:	n/a	n/a

(count:244 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:120935804-120935854	HMEC	breast:	n/a
2	chr7:120852287-120852337	HAEpiC	amniotic membrane:	n/a
3	chr7:120903952-120904002	HEEpiC	esophagus:	n/a
4	chr7:120935804-120935854	AG10803	skin:	n/a
5	chr7:120903952-120904002	PrEC	prostate:	n/a
6	chr7:120903952-120904002	HL-60	blood:	n/a
7	chr7:120852287-120852337	SK-N-MC	brain:	n/a
8	chr7:120903952-120904002	ovcar-3	ovarian:	n/a
9	chr7:120852287-120852337	NB4	blood:	n/a
10	chr7:120903952-120904002	HRPEpiC	eye:	n/a
11	chr7:120903952-120904002	HMEC	breast:	n/a
12	chr7:120852287-120852337	SKMC	muscle:	n/a
13	chr7:120935804-120935854	A549	lung:	n/a
14	chr7:120918492-120918542	AG09319	gingival:	n/a
15	chr7:120935804-120935854	NHBE	bronchial:	n/a
16	chr7:120918492-120918542	NH-A	brain:	n/a
17	chr7:120935804-120935854	GM12892	blood:	n/a
18	chr7:120935804-120935854	MCF-7	breast:	n/a
19	chr7:120852287-120852337	HUVEC	blood vessel:	n/a
20	chr7:120935804-120935854	SK-N-SH_RA	brain:	n/a
21	chr7:120903952-120904002	MCF-7	breast:	n/a
22	chr7:120903952-120904002	HRE	kidney:	n/a
23	chr7:120903952-120904002	T-47D	breast:	n/a
24	chr7:120852287-120852337	AG09319	gingival:	n/a
25	chr7:120903952-120904002	GM19239	blood:	n/a
26	chr7:120852287-120852337	Caco-2	colon:	n/a
27	chr7:120918492-120918542	HepG2	liver:	n/a
28	chr7:120935804-120935854	LNCaP	prostate:	n/a
29	chr7:120918492-120918542	HCT-116	colon:	n/a
30	chr7:120935804-120935854	HCPEpiC	choroid plexus:	n/a
31	chr7:120852287-120852337	ProgFib	skin:	n/a
32	chr7:120935804-120935854	GM12878	blood:	n/a
33	chr7:120903952-120904002	ProgFib	skin:	n/a
34	chr7:120852287-120852337	HRE	kidney:	n/a
35	chr7:120918492-120918542	NT2-D1	testis:	n/a
36	chr7:120918492-120918542	GM12891	blood:	n/a
37	chr7:120852287-120852337	GM12892	blood:	n/a
38	chr7:120852287-120852337	Hepatocyte	liver:	n/a
39	chr7:120935804-120935854	Hepatocyte	liver:	n/a
40	chr7:120918492-120918542	GM12892	blood:	n/a
41	chr7:120903952-120904002	HNPCEpiC	eye:	n/a
42	chr7:120852287-120852337	BE2_C	brain:	n/a
43	chr7:120852287-120852337	BJ	skin:	n/a
44	chr7:120918492-120918542	Jurkat	blood:	n/a
45	chr7:120852287-120852337	K562	blood:	n/a
46	chr7:120918492-120918542	SAEC	small airway:	n/a
47	chr7:120918492-120918542	A549	lung:	n/a
48	chr7:120852287-120852337	SK-N-SH_RA	brain:	n/a
49	chr7:120935804-120935854	RPTEC	kidney:	n/a
50	chr7:120903952-120904002	NHDF-neo	bronchial:	n/a

(count:168 , 50 per page) page: 1 2 3 4

No.	Distal block	Cell Line	Cell type
1	chr7:120848908..120852746-chr7:120854048..120856854,5	K562	blood:
2	chr7:120775298..120777729-chr7:120784980..120787236,2	K562	blood:
3	chr7:120776773..120780025-chr7:120780036..120783879,5	K562	blood:
4	chr7:120826513..120828364-chr7:120831445..120833082,2	K562	blood:
5	chr7:120868481..120870338-chr7:120872297..120875239,2	K562	blood:
6	chr7:120776773..120780025-chr7:120780036..120783879,5	K562	blood:
7	chr7:120836283..120838682-chr7:120872699..120875576,2	K562	blood:
8	chr7:120795773..120797824-chr7:120798929..120800429,2	K562	blood:
9	chr7:120748117..120751439-chr7:120760191..120762453,3	K562	blood:
10	chr7:120748117..120751439-chr7:120760191..120762453,3	K562	blood:
11	chr7:120778509..120781370-chr7:120785067..120788347,3	K562	blood:
12	chr7:120896920..120901012-chr7:120903839..120905762,5	K562	blood:
13	chr7:120589479..120591049-chr7:120760761..120762508,2	MCF-7	breast:
14	chr7:120841468..120846547-chr7:120846758..120854034,8	K562	blood:
15	chr7:120795773..120797824-chr7:120798929..120800429,2	K562	blood:
16	chr7:120903478..120907349-chr7:120909613..120913573,4	K562	blood:
17	chr7:120783598..120786251-chr7:120808569..120811529,2	K562	blood:
18	chr7:120787470..120791175-chr7:120804388..120809200,4	K562	blood:
19	chr7:120858530..120860172-chr7:120865997..120868025,2	K562	blood:
20	chr7:120853643..120855944-chr7:120855960..120858802,3	K562	blood:
21	chr7:120831876..120833803-chr7:120835458..120837128,2	K562	blood:
22	chr7:120902142..120904309-chr7:120913749..120915446,2	K562	blood:
23	chr7:120778509..120781370-chr7:120785067..120788347,3	K562	blood:
24	chr7:120853643..120855944-chr7:120855960..120858802,3	K562	blood:
25	chr7:120896920..120901012-chr7:120903839..120905762,5	K562	blood:
26	chr7:120765203..120766976-chr7:120768801..120771594,2	K562	blood:
27	chr7:120879517..120881082-chr7:120883141..120886021,2	K562	blood:
28	chr7:120651629..120654433-chr7:120773346..120775726,2	K562	blood:
29	chr7:120598328..120601764-chr7:120747067..120750480,4	K562	blood:
30	chr7:120788426..120790789-chr7:120791125..120793163,2	K562	blood:
31	chr7:120879517..120881994-chr7:120882337..120885417,3	K562	blood:
32	chr7:120903478..120907349-chr7:120909613..120913573,4	K562	blood:
33	chr7:120841468..120846547-chr7:120846758..120854034,8	K562	blood:
34	chr7:120770037..120772769-chr7:120796157..120798436,2	K562	blood:
35	chr7:120821041..120822740-chr7:120822872..120826535,3	K562	blood:
36	chr7:117822911..117825721-chr7:120917974..120920146,2	K562	blood:
37	chr7:120921526..120923763-chr7:120928697..120931385,3	K562	blood:
38	chr7:120753655..120756147-chr7:120756373..120757912,2	K562	blood:
39	chr7:120817633..120820415-chr7:120824937..120827209,2	K562	blood:
40	chr7:120892571..120894403-chr7:120897763..120901002,3	K562	blood:
41	chr7:120865059..120868027-chr7:120873539..120876045,2	K562	blood:
42	chr7:120628746..120630644-chr7:120748164..120750985,2	K562	blood:
43	chr7:120873011..120874844-chr7:120878339..120881386,3	K562	blood:
44	chr7:120856242..120858668-chr7:120894112..120895725,2	K562	blood:
45	chr7:120626686..120628740-chr7:120746587..120749245,2	K562	blood:
46	chr7:120836283..120838682-chr7:120872699..120875576,2	K562	blood:
47	chr7:120854329..120856810-chr7:120876127..120877752,2	K562	blood:
48	chr7:120910860..120914129-chr7:120914551..120916811,3	K562	blood:
49	chr7:120811226..120812887-chr7:120837406..120839127,2	K562	blood:
50	chr7:120741938..120744145-chr7:120762816..120764575,2	K562	blood:

No data

Variant related genes	Relation type
RNU6-517P	TF binding region
CPED1	TF binding region
RNU6-517P	CpG island
CPED1	CpG island
ENSG00000071243	chromatin interactions
ENSG00000207090	chromatin interactions
ENSG00000196937	chromatin interactions
ENSG00000106034	chromatin interactions
ENSG00000128534	chromatin interactions

Extended variants
information (count: 6643 )
Associated
traits (count: 96 )

Variant overlapped rSNPs/rCNVs (count:6643 , 50 per page) page: 1 2 3 4 5 6 7 ... 133

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs187825818	chr7:120749175-120749176	Enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs139108433	chr7:120749182-120749183	Enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs74405429	chr7:120749199-120749200	Enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs530645231	chr7:120749251-120749252	Enhancers Flanking Active TSS Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs550662579	chr7:120749265-120749266	Enhancers Flanking Active TSS Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs191529913	chr7:120749302-120749303	Enhancers Flanking Active TSS Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs183675385	chr7:120749339-120749340	Enhancers Flanking Active TSS Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs188729124	chr7:120749351-120749352	Enhancers Flanking Active TSS Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs145030563	chr7:120749360-120749361	Enhancers Flanking Active TSS Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs181120425	chr7:120749431-120749432	Enhancers Flanking Active TSS Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs528731427	chr7:120749438-120749439	Enhancers Flanking Active TSS Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs558548594	chr7:120749511-120749512	Enhancers Flanking Active TSS Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs568874884	chr7:120749522-120749523	Enhancers Flanking Active TSS Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs539013152	chr7:120749565-120749566	Enhancers Flanking Active TSS Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs79035321	chr7:120749572-120749573	Enhancers Flanking Active TSS Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs369587229	chr7:120749581-120749582	Enhancers Flanking Active TSS Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs185182056	chr7:120749603-120749604	Enhancers Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs142168082	chr7:120749614-120749615	Enhancers Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs144523072	chr7:120749629-120749630	Enhancers Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs573179364	chr7:120749653-120749654	Enhancers Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs190418583	chr7:120749655-120749656	Enhancers Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs147840164	chr7:120749679-120749680	Enhancers Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs181692672	chr7:120749698-120749699	Enhancers Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs548158786	chr7:120749736-120749737	Enhancers Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs560819726	chr7:120749742-120749743	Enhancers Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs530361607	chr7:120749837-120749838	Enhancers Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs374426122	chr7:120749848-120749849	Enhancers Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs546879786	chr7:120749873-120749874	Enhancers Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs116227728	chr7:120749967-120749968	Enhancers Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs186385445	chr7:120749986-120749987	Enhancers Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs190787622	chr7:120749987-120749988	Enhancers Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs552859401	chr7:120750002-120750003	Enhancers Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs568938991	chr7:120750043-120750044	Enhancers Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs17626220	chr7:120750159-120750160	Enhancers Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs142351586	chr7:120750168-120750169	Enhancers Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs116118218	chr7:120750174-120750175	Enhancers Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs180905708	chr7:120750182-120750183	Enhancers Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs143224436	chr7:120750271-120750272	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs573041270	chr7:120750278-120750279	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs535207782	chr7:120750284-120750285	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs538970098	chr7:120750325-120750326	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs558871523	chr7:120750406-120750407	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs374841745	chr7:120750429-120750430	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs530975534	chr7:120750464-120750465	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs377372596	chr7:120750465-120750466	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs543857688	chr7:120750501-120750502	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs560901844	chr7:120750517-120750518	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs574467646	chr7:120750532-120750533	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs540285523	chr7:120750560-120750561	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs148294126	chr7:120750595-120750596	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:96)

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
Autism	22495311	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
Metanephric adenoma	20802469	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Burkitt''s lymphoma	19759907	CNVD
Myelodysplastic syndrome	21251322	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
Biliary cancer	19435499	CNVD
Non-small cell lung cancer	21829676	CNVD
Ovarian neoplasms	16753589	CNVD
Prostate cancer	23792589	CNVD
Adenocarcinoma	21044232	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Non-small cell lung cancer	19889201	CNVD
Acute myeloid leukemia	18000384	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Metastatic melanoma	18483359	CNVD
Autism	18414403	CNVD
Autism	19401682	CNVD
Autism	19546859	CNVD
Schizophrenia	19546859	CNVD
Tourette syndrome	19546859	CNVD
Melanoma	19188590	CNVD
Glioblastoma multiforme	22286061	CNVD
Glioblastoma multiforme	21922591	CNVD
Hepatocellular carcinoma	16785998	CNVD
Glioblastoma multiforme	18628472	CNVD
Myelofibrosis	22110671	CNVD
Renal cell carcinoma	18194544	CNVD
Basal cell lymphoma	21115979	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21509527	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Cancer	20164919	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Breast cancer	22522925	CNVD
Melanoma	20877625	CNVD
Ovarian cancer	21781307	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Splenic marginal zone lymphoma	18492102	CNVD
Barrett''s adenocarcinoma	18663352	CNVD

Chromatin state (count:1241 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:120711400-120790600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
2	chr7:120725800-120761800	Weak transcription	Fetal Stomach	stomach
3	chr7:120727800-120756400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
4	chr7:120735400-120784000	Weak transcription	Right Ventricle	heart
5	chr7:120738200-120749200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
6	chr7:120740400-120753000	Weak transcription	Osteobl	bone
7	chr7:120740600-120758800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
8	chr7:120740800-120786000	Weak transcription	Fetal Lung	lung
9	chr7:120741400-120782200	Weak transcription	Duodenum Smooth Muscle	Duodenum
10	chr7:120741800-120765600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
11	chr7:120742000-120810000	Weak transcription	Psoas Muscle	Psoas
12	chr7:120742800-120752000	Weak transcription	Aorta	Aorta
13	chr7:120742800-120765000	Weak transcription	NHDF-Ad	bronchial
14	chr7:120742800-120771800	Weak transcription	Stomach Smooth Muscle	stomach
15	chr7:120743000-120750600	Weak transcription	Ovary	ovary
16	chr7:120743000-120765400	Weak transcription	Left Ventricle	heart
17	chr7:120743000-120784200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
18	chr7:120743400-120778200	Strong transcription	K562	blood
19	chr7:120743600-120752800	Weak transcription	HMEC	breast
20	chr7:120743800-120753200	Weak transcription	HSMMtube	muscle
21	chr7:120743800-120765600	Weak transcription	Skeletal Muscle Female	skeletal muscle
22	chr7:120745600-120749200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
23	chr7:120746200-120768000	Weak transcription	Skeletal Muscle Male	skeletal muscle
24	chr7:120746200-120777800	Weak transcription	Rectal Smooth Muscle	rectum
25	chr7:120746400-120750200	Weak transcription	NHLF	lung
26	chr7:120747400-120752000	Weak transcription	Liver	Liver
27	chr7:120748000-120749800	Enhancers	iPS-20b Cell Line	embryonic stem cell
28	chr7:120748000-120750000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
29	chr7:120748200-120749200	Weak transcription	Muscle Satellite Cultured Cells	--
30	chr7:120748200-120752600	Weak transcription	Adipose Nuclei	Adipose
31	chr7:120748800-120749200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
32	chr7:120748800-120749600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
33	chr7:120748800-120750200	Enhancers	ES-I3 Cell Line	embryonic stem cell
34	chr7:120748800-120755000	Strong transcription	HSMM	muscle
35	chr7:120749000-120749400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
36	chr7:120749000-120749400	Enhancers	Brain Cingulate Gyrus	brain
37	chr7:120749000-120749600	Enhancers	iPS-18 Cell Line	embryonic stem cell
38	chr7:120749200-120749600	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
39	chr7:120749200-120749600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
40	chr7:120749200-120749600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
41	chr7:120749200-120749800	Enhancers	HUES64 Cell Line	embryonic stem cell
42	chr7:120749200-120750200	Enhancers	Muscle Satellite Cultured Cells	--
43	chr7:120749600-120750200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
44	chr7:120749600-120752800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
45	chr7:120750200-120751200	Strong transcription	NHLF	lung
46	chr7:120750200-120753200	Weak transcription	Muscle Satellite Cultured Cells	--
47	chr7:120750600-120753400	Strong transcription	Ovary	ovary
48	chr7:120751200-120756000	Weak transcription	NHLF	lung
49	chr7:120752000-120752200	ZNF genes & repeats	Aorta	Aorta
50	chr7:120752000-120752800	Strong transcription	Liver	Liver

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