Variant report

Variant	nsv606706
Chromosome Location	chr7:40018693-40133044
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:798)
CpG islands
(count:184)
Chromatin interactive
region (count:71)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:798 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:40110475-40110675	K562	blood:	n/a	n/a
2	ARID3A	chr7:40092188-40092405	HepG2	liver:	n/a	n/a
3	ARID3A	chr7:40048432-40048455	K562	blood:	n/a	n/a
4	ARID3A	chr7:40098322-40098610	K562	blood:	n/a	n/a
5	ATF1	chr7:40117561-40117768	K562	blood:	n/a	n/a
6	ATF3	chr7:40096977-40097167	K562	blood:	n/a	n/a
7	BACH1	chr7:40098271-40098628	H1-hESC	embryonic stem cell:	n/a	n/a
8	BACH1	chr7:40078099-40078178	K562	blood:	n/a	n/a
9	BACH1	chr7:40098245-40098605	K562	blood:	n/a	n/a
10	BHLHE40	chr7:40096875-40097314	K562	blood:	n/a	n/a
11	BHLHE40	chr7:40098417-40098988	K562	blood:	n/a	n/a
12	BHLHE40	chr7:40092120-40092431	GM12878	blood:	n/a	n/a
13	BRCA1	chr7:40030603-40030622	Hela-S3	cervix:	n/a	n/a
14	CBX3	chr7:40096872-40097273	K562	blood:	n/a	n/a
15	CEBPB	chr7:40047754-40048150	IMR90	lung:	n/a	n/a
16	CEBPB	chr7:40124115-40124426	HepG2	liver:	n/a	chr7:40124257-40124268
17	CEBPB	chr7:40023284-40023561	A549	lung:	n/a	chr7:40023439-40023450
18	CEBPB	chr7:40082093-40082233	K562	blood:	n/a	chr7:40082133-40082144
19	CEBPB	chr7:40052756-40053137	K562	blood:	n/a	chr7:40052935-40052946
20	CEBPB	chr7:40114247-40114475	H1-hESC	embryonic stem cell:	n/a	chr7:40114370-40114381
21	CEBPB	chr7:40046274-40046386	K562	blood:	n/a	n/a
22	CEBPB	chr7:40104587-40104830	K562	blood:	n/a	chr7:40104687-40104700 chr7:40104689-40104698 chr7:40104687-40104698 chr7:40104687-40104700 chr7:40104689-40104698 chr7:40104689-40104698 chr7:40104689-40104698 chr7:40104686-40104703 chr7:40104688-40104699
23	CEBPB	chr7:40028548-40028593	IMR90	lung:	n/a	n/a
24	CEBPB	chr7:40114217-40114443	A549	lung:	n/a	chr7:40114370-40114381
25	CEBPB	chr7:40117500-40117833	K562	blood:	n/a	n/a
26	CEBPB	chr7:40023285-40023485	HepG2	liver:	n/a	chr7:40023439-40023450
27	CEBPB	chr7:40117525-40117828	A549	lung:	n/a	n/a
28	CEBPB	chr7:40028089-40028276	HepG2	liver:	n/a	n/a
29	CEBPB	chr7:40019391-40019644	H1-hESC	embryonic stem cell:	n/a	n/a
30	CEBPB	chr7:40082068-40082213	HepG2	liver:	n/a	chr7:40082133-40082144
31	CEBPB	chr7:40040422-40040696	IMR90	lung:	n/a	n/a
32	CEBPB	chr7:40104549-40104819	IMR90	lung:	n/a	chr7:40104687-40104700 chr7:40104689-40104698 chr7:40104687-40104698 chr7:40104687-40104700 chr7:40104689-40104698 chr7:40104689-40104698 chr7:40104689-40104698 chr7:40104686-40104703 chr7:40104688-40104699
33	CEBPB	chr7:40028537-40028686	K562	blood:	n/a	n/a
34	CEBPB	chr7:40052800-40053114	IMR90	lung:	n/a	chr7:40052935-40052946
35	CEBPB	chr7:40028054-40028261	A549	lung:	n/a	n/a
36	CEBPB	chr7:40117519-40117821	Hela-S3	cervix:	n/a	n/a
37	CEBPB	chr7:40047766-40048133	Hela-S3	cervix:	n/a	n/a
38	CEBPB	chr7:40082049-40082293	HepG2	liver:	n/a	chr7:40082133-40082144
39	CEBPB	chr7:40052781-40053133	A549	lung:	n/a	chr7:40052935-40052946
40	CEBPB	chr7:40117557-40117777	H1-hESC	embryonic stem cell:	n/a	n/a
41	CEBPB	chr7:40117514-40117763	K562	blood:	n/a	n/a
42	CEBPB	chr7:40117497-40117807	HepG2	liver:	n/a	n/a
43	CEBPB	chr7:40052763-40053118	HepG2	liver:	n/a	chr7:40052935-40052946
44	CEBPB	chr7:40114299-40114406	Hela-S3	cervix:	n/a	chr7:40114370-40114381
45	CEBPB	chr7:40104584-40104827	A549	lung:	n/a	chr7:40104687-40104700 chr7:40104689-40104698 chr7:40104687-40104698 chr7:40104687-40104700 chr7:40104689-40104698 chr7:40104689-40104698 chr7:40104689-40104698 chr7:40104686-40104703 chr7:40104688-40104699
46	CEBPB	chr7:40114213-40114488	IMR90	lung:	n/a	chr7:40114370-40114381
47	CEBPB	chr7:40117517-40117829	IMR90	lung:	n/a	n/a
48	CEBPB	chr7:40117544-40117798	K562	blood:	n/a	n/a
49	CEBPB	chr7:40023284-40023543	K562	blood:	n/a	chr7:40023439-40023450
50	CEBPB	chr7:40028039-40028275	IMR90	lung:	n/a	n/a

(count:184 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:40047674-40047724	PFSK-1	brain:	n/a
2	chr7:40047674-40047724	PFSK-1	brain:	n/a
3	chr7:40098119-40098169	HAEpiC	amniotic membrane:	n/a
4	chr7:40047674-40047724	HMEC	breast:	n/a
5	chr7:40026390-40026440	SK-N-MC	brain:	n/a
6	chr7:40098119-40098169	K562	blood:	n/a
7	chr7:40026390-40026440	LNCaP	prostate:	n/a
8	chr7:40026390-40026440	NB4	blood:	n/a
9	chr7:40047674-40047724	NB4	blood:	n/a
10	chr7:40047674-40047724	Hela-S3	cervix:	n/a
11	chr7:40047674-40047724	NH-A	brain:	n/a
12	chr7:40026390-40026440	IMR90	lung:	fetal
13	chr7:40098119-40098169	SAEC	small airway:	n/a
14	chr7:40047674-40047724	Hepatocyte	liver:	n/a
15	chr7:40026390-40026440	MCF10A-Er-Src	breast:	n/a
16	chr7:40098119-40098169	SKMC	muscle:	n/a
17	chr7:40098119-40098169	SK-N-SH	brain:	n/a
18	chr7:40047674-40047724	SAEC	small airway:	n/a
19	chr7:40047674-40047724	MCF-7	breast:	n/a
20	chr7:40047674-40047724	AoSMC	blood vessel:	n/a
21	chr7:40098119-40098169	HL-60	blood:	n/a
22	chr7:40098119-40098169	NB4	blood:	n/a
23	chr7:40098119-40098169	NHDF-neo	bronchial:	n/a
24	chr7:40047674-40047724	AG10803	skin:	n/a
25	chr7:40047674-40047724	HRPEpiC	eye:	n/a
26	chr7:40098119-40098169	PFSK-1	brain:	n/a
27	chr7:40047674-40047724	ProgFib	skin:	n/a
28	chr7:40098119-40098169	HMEC	breast:	n/a
29	chr7:40047674-40047724	GM06990	blood:	n/a
30	chr7:40026390-40026440	CMK	blood:	n/a
31	chr7:40098119-40098169	Jurkat	blood:	n/a
32	chr7:40047674-40047724	AG09319	gingival:	n/a
33	chr7:40047674-40047724	K562	blood:	n/a
34	chr7:40047674-40047724	GM19239	blood:	n/a
35	chr7:40098119-40098169	H1-hESC	embryonic stem cell:	embryo
36	chr7:40026390-40026440	AoSMC	blood vessel:	n/a
37	chr7:40047674-40047724	MCF10A-Er-Src	breast:	n/a
38	chr7:40098119-40098169	BE2_C	brain:	n/a
39	chr7:40047674-40047724	HCPEpiC	choroid plexus:	n/a
40	chr7:40098119-40098169	HCF	heart:	n/a
41	chr7:40047674-40047724	HRCEpiC	kidney:	n/a
42	chr7:40098119-40098169	Hela-S3	cervix:	n/a
43	chr7:40026390-40026440	RPTEC	kidney:	n/a
44	chr7:40098119-40098169	AG04450	lung:	fetal
45	chr7:40026390-40026440	HEK293	kidney:	embryo
46	chr7:40047674-40047724	GM12878	blood:	n/a
47	chr7:40098119-40098169	U87	brain:	n/a
48	chr7:40098119-40098169	AG04449	skin:	fetal
49	chr7:40026390-40026440	BE2_C	brain:	n/a
50	chr7:40047674-40047724	ECC-1	luminal epithelium:	n/a

(count:71 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr7:40080571..40083008-chr7:40084879..40087447,2	MCF-7	breast:
2	chr7:40109257..40111529-chr7:40116739..40118703,2	K562	blood:
3	chr7:39784501..39786932-chr7:40060004..40061750,2	MCF-7	breast:
4	chr7:40030873..40032517-chr7:40032744..40035272,2	MCF-7	breast:
5	chr7:39987662..39991169-chr7:40080646..40083080,4	MCF-7	breast:
6	chr7:40080571..40083008-chr7:40084879..40087447,2	MCF-7	breast:
7	chr7:39995562..39997587-chr7:40034318..40036710,2	MCF-7	breast:
8	chr7:40048646..40050601-chr7:40053388..40055304,2	K562	blood:
9	chr7:39987353..39988943-chr7:40114287..40116137,2	K562	blood:
10	chr7:40030873..40032517-chr7:40032744..40035272,2	MCF-7	breast:
11	chr7:40098014..40099578-chr7:40101201..40104032,2	K562	blood:
12	chr7:40031268..40032823-chr7:40035953..40037510,2	MCF-7	breast:
13	chr7:39988550..39991713-chr7:40061558..40063608,3	K562	blood:
14	chr7:39988360..39989993-chr7:40043124..40045978,3	MCF-7	breast:
15	chr7:39935762..39936421-chr7:40091763..40092363,2	K562	blood:
16	chr7:39988782..39993568-chr7:40089798..40094373,7	MCF-7	breast:
17	chr7:40084390..40086552-chr7:40091089..40093935,3	K562	blood:
18	chr7:40055192..40057711-chr7:40058795..40061552,3	K562	blood:
19	chr7:39992705..39994767-chr7:40040920..40043283,2	K562	blood:
20	chr7:40132356..40134649-chr7:40137450..40139023,2	K562	blood:
21	chr7:40059026..40061512-chr7:40062237..40065156,2	MCF-7	breast:
22	chr7:40088024..40089904-chr7:40091053..40093923,2	MCF-7	breast:
23	chr7:40016185..40017725-chr7:40028366..40031128,2	K562	blood:
24	chr7:40084993..40087566-chr7:40090698..40092927,2	K562	blood:
25	chr7:40038038..40041383-chr7:40051581..40055589,3	K562	blood:
26	chr7:40115479..40117853-chr7:40121950..40124630,2	MCF-7	breast:
27	chr7:40084390..40086552-chr7:40091089..40093935,3	K562	blood:
28	chr7:39987621..39991955-chr7:40089379..40093722,6	MCF-7	breast:
29	chr7:39986728..39990828-chr7:40016183..40019996,4	MCF-7	breast:
30	chr7:39987746..39990922-chr7:40055976..40057979,3	K562	blood:
31	chr7:40090602..40093136-chr7:40095056..40097125,2	K562	blood:
32	chr7:39619647..39620204-chr7:40092201..40092766,2	K562	blood:
33	chr7:40025445..40027288-chr7:40029164..40032016,2	K562	blood:
34	chr7:40109167..40111821-chr7:40114946..40117693,2	K562	blood:
35	chr7:39986663..39989008-chr7:40035472..40037902,2	K562	blood:
36	chr7:40025445..40027288-chr7:40029164..40032016,2	K562	blood:
37	chr7:39988014..39992779-chr7:40016991..40021232,5	K562	blood:
38	chr7:40038956..40041383-chr7:40052873..40055589,2	K562	blood:
39	chr7:40059026..40061512-chr7:40062237..40065156,2	MCF-7	breast:
40	chr7:40093916..40096892-chr7:40098882..40101191,2	K562	blood:
41	chr7:40048549..40051232-chr7:40060255..40062264,2	K562	blood:
42	chr7:40115479..40117853-chr7:40121950..40124630,2	MCF-7	breast:
43	chr17:59501958..59502789-chr7:40112228..40112887,2	MCF-7	breast:
44	chr7:39988605..39990899-chr7:40070252..40072464,2	K562	blood:
45	chr7:39987767..39989590-chr7:40096379..40098788,2	K562	blood:
46	chr7:40031268..40032823-chr7:40035953..40037510,2	MCF-7	breast:
47	chr7:39987287..39990526-chr7:40030076..40032814,4	MCF-7	breast:
48	chr7:40084993..40087566-chr7:40090698..40092927,2	K562	blood:
49	chr7:39988482..39990728-chr7:40029986..40032615,2	MCF-7	breast:
50	chr7:40105682..40108224-chr7:40109570..40112415,2	K562	blood:

No data

Variant related genes	Relation type
CDK13	TF binding region
CDK13	CpG island
ENSG00000110063	chromatin interactions
ENSG00000259826	chromatin interactions
ENSG00000065883	chromatin interactions

Extended variants
information (count: 4427 )
Associated
traits (count: 84 )

Variant overlapped rSNPs/rCNVs (count:4427 , 50 per page) page: 1 2 3 4 5 6 7 ... 89

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10275367	chr7:40018693-40018694	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs545914611	chr7:40018697-40018698	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs555872019	chr7:40018714-40018715	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs188054350	chr7:40018744-40018745	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs116775379	chr7:40018751-40018752	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs561254150	chr7:40018789-40018790	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs193083260	chr7:40018793-40018794	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs113468967	chr7:40018811-40018812	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs370997296	chr7:40018815-40018816	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs113388540	chr7:40018816-40018817	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs372063206	chr7:40018820-40018821	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs11979592	chr7:40018821-40018822	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs150030435	chr7:40018845-40018846	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs529034575	chr7:40018932-40018933	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs557497008	chr7:40018976-40018977	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs532484728	chr7:40018978-40018979	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs144958658	chr7:40018987-40018988	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs569153004	chr7:40019109-40019110	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs531735291	chr7:40019124-40019125	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs185531274	chr7:40019145-40019146	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs568379525	chr7:40019174-40019175	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs533947009	chr7:40019193-40019194	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs142028052	chr7:40019219-40019220	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs570661475	chr7:40019238-40019239	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs373908724	chr7:40019246-40019247	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs554075400	chr7:40019297-40019298	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs187910281	chr7:40019299-40019300	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs145777534	chr7:40019317-40019318	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs541437272	chr7:40019376-40019377	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs376857452	chr7:40019377-40019378	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs192052495	chr7:40019557-40019558	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs574770536	chr7:40019612-40019613	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs540558820	chr7:40019613-40019614	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs371489801	chr7:40019677-40019678	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs532786923	chr7:40019685-40019686	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs545931464	chr7:40019711-40019712	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs563011349	chr7:40019712-40019713	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs147759077	chr7:40019739-40019740	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs548625761	chr7:40019745-40019746	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs568497342	chr7:40019889-40019890	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs527571257	chr7:40019935-40019936	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs374731015	chr7:40019946-40019947	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs184601678	chr7:40019957-40019958	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs17171636	chr7:40019969-40019970	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs542751812	chr7:40019985-40019986	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs11981251	chr7:40020026-40020027	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs567310220	chr7:40020032-40020033	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs555949620	chr7:40020041-40020042	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs188627456	chr7:40020050-40020051	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs535199686	chr7:40020110-40020111	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:84)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Lynch syndrome	18415027	CNVD
Biliary cancer	19435499	CNVD
Cancer	16751803	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Wilms tumour	21544195	CNVD
Glioblastoma multiforme	17387387	CNVD
Astrocytoma	17387387	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	18923191	CNVD
Glioma	21971842	CNVD
Glioblastoma multiforme	21080181	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Oral cancer	21386901	CNVD
colon cancer	17210682	CNVD
Lung adenocarcinoma	21810691	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Colorectal cancer	19359472	CNVD
Hypothalamic hamartomas	18252217	CNVD
Human rectal carcinomas	16397240	CNVD
Peripheral t-cell lymphoma	19118030	CNVD
Medulloblastoma	18056178	CNVD
Basal cell lymphoma	17170743	CNVD
Ewing''s sarcoma	21437220	CNVD
Thyroid cancer	19087340	CNVD
Seminomas	18059402	CNVD
Testicular cancer	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	19415332	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
Stenocardia	21860640	CNVD
Vasospasm	21860640	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Lung cancer	18438408	CNVD
lymphocytic leukemia	21291569	CNVD
Autism	22495311	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Cancer	21637783	CNVD
Squamous cell cancer	20885788	CNVD
Breast cancer	16397240	CNVD
Non-small cell lung cancer	21829676	CNVD
Glioblastoma multiforme	17002787	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Glioblastoma multiforme	18628472	CNVD
Cancer	21183584	CNVD
Breast cancer	21785460	CNVD
Follicular lymphoma	20505157	CNVD
Williams-beuren syndrome	22470819	CNVD
Renal cell carcinoma	18765545	CNVD
Breast cancer	21364760	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute myeloid leukemia	21251322	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Multiple myeloma	16461302	CNVD
Glioblastoma multiforme	21750150	CNVD
Hepatocellular carcinoma	16750200	CNVD
Prostate cancer	18632612	CNVD
Acute myeloid leukemia	17237825	CNVD
Breast cancer	17899364	CNVD
Breast cancer	20409316	CNVD
Acute monocytic leukemia	16498392	CNVD
Myelofibrosis	22110671	CNVD
Colorectal cancer	21645411	CNVD
Colorectal cancer	19455253	CNVD
Glioblastoma multiforme	22286061	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Gastric cancer	24379144	CNVD
small cell lung cancer	20016488	CNVD
abnormal development	18461090	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Bladder cancer	21909424	CNVD
Breast cancer	22522925	CNVD
Schizophrenia	21346763	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:2925 , 50 per page) page: 1 2 3 4 5 6 7 ... 59

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:39993600-40048200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
2	chr7:39994200-40027200	Weak transcription	HSMM	muscle
3	chr7:39995200-40042600	Weak transcription	K562	blood
4	chr7:39997800-40027400	Weak transcription	Duodenum Mucosa	Duodenum
5	chr7:39998000-40027200	Weak transcription	Hela-S3	cervix
6	chr7:40005600-40021000	Enhancers	Primary T helper cells PMA-I stimulated	--
7	chr7:40005600-40021000	Enhancers	Primary T helper cells fromperipheralblood	blood
8	chr7:40006600-40019800	Enhancers	Primary B cells from peripheral blood	blood
9	chr7:40006800-40031200	Weak transcription	Fetal Stomach	stomach
10	chr7:40007200-40027200	Weak transcription	Cortex derived primary cultured neurospheres	brain
11	chr7:40007600-40027200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
12	chr7:40009400-40020800	Enhancers	Primary T killer naive cells fromperipheralblood	blood
13	chr7:40009400-40027200	Weak transcription	Rectal Mucosa Donor 29	rectum
14	chr7:40009400-40027400	Weak transcription	Osteobl	bone
15	chr7:40009600-40027400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
16	chr7:40009800-40027200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
17	chr7:40010000-40024600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
18	chr7:40010000-40026800	Weak transcription	NHEK	skin
19	chr7:40010200-40025000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
20	chr7:40010400-40027200	Weak transcription	Esophagus	oesophagus
21	chr7:40011000-40021000	Enhancers	Primary T regulatory cells fromperipheralblood	blood
22	chr7:40011200-40023600	Weak transcription	Lung	lung
23	chr7:40011200-40025400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
24	chr7:40011400-40027400	Weak transcription	Fetal Muscle Trunk	muscle
25	chr7:40014200-40021200	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
26	chr7:40014800-40021200	Enhancers	Primary T helper naive cells from peripheral blood	blood
27	chr7:40015000-40023600	Weak transcription	Fetal Intestine Small	intestine
28	chr7:40015800-40019200	Enhancers	Breast Myoepithelial Primary Cells	Breast
29	chr7:40015800-40019200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
30	chr7:40016000-40019000	Weak transcription	Pancreas	Pancrea
31	chr7:40016000-40021000	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
32	chr7:40016200-40020200	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
33	chr7:40016400-40019600	Enhancers	Primary T cells fromperipheralblood	blood
34	chr7:40016400-40020200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
35	chr7:40016600-40019400	Enhancers	Brain Substantia Nigra	brain
36	chr7:40016600-40019400	Enhancers	Dnd41	blood
37	chr7:40016600-40019600	Enhancers	Brain Angular Gyrus	brain
38	chr7:40016600-40019800	Enhancers	Brain Hippocampus Middle	brain
39	chr7:40016600-40020400	Enhancers	Colon Smooth Muscle	Colon
40	chr7:40016600-40021000	Enhancers	H1 Cell Line	embryonic stem cell
41	chr7:40016800-40018800	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
42	chr7:40016800-40019200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
43	chr7:40016800-40020000	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
44	chr7:40016800-40027200	Weak transcription	A549	lung
45	chr7:40017200-40018800	Enhancers	Primary B cells from cord blood	blood
46	chr7:40017200-40019400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
47	chr7:40017200-40019800	Enhancers	Skeletal Muscle Female	skeletal muscle
48	chr7:40017400-40018800	Flanking Active TSS	HUES64 Cell Line	embryonic stem cell
49	chr7:40017400-40018800	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
50	chr7:40017400-40018800	Enhancers	Primary hematopoietic stem cells short term culture	blood

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