Variant report

Variant	nsv888828
Chromosome Location	chr7:101921289-101939759
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1386)
CpG islands
(count:1283)
Chromatin interactive
region (count:79)
LncRNA
region (count:0)
Mature miRNA
region (count: 1)
miRNA target
sites (count:0)

(count:1386 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr7:101934447-101935309	GM12878	blood:	n/a	n/a
2	ATF2	chr7:101932194-101932667	GM12878	blood:	n/a	n/a
3	ATF2	chr7:101933023-101933334	H1-hESC	embryonic stem cell:	n/a	n/a
4	ATF2	chr7:101932966-101933741	GM12878	blood:	n/a	n/a
5	ATF2	chr7:101934617-101935095	GM12878	blood:	n/a	n/a
6	ATF2	chr7:101927669-101928058	GM12878	blood:	n/a	n/a
7	ATF2	chr7:101927721-101928042	GM12878	blood:	n/a	n/a
8	BACH1	chr7:101922731-101923023	H1-hESC	embryonic stem cell:	n/a	n/a
9	BACH1	chr7:101933088-101933320	H1-hESC	embryonic stem cell:	n/a	n/a
10	BACH1	chr7:101929768-101929916	K562	blood:	n/a	n/a
11	BACH1	chr7:101935061-101935073	H1-hESC	embryonic stem cell:	n/a	n/a
12	BACH1	chr7:101930205-101930668	H1-hESC	embryonic stem cell:	n/a	n/a
13	BACH1	chr7:101929546-101929960	H1-hESC	embryonic stem cell:	n/a	n/a
14	BATF	chr7:101934842-101935198	GM12878	blood:	n/a	n/a
15	BATF	chr7:101927734-101927953	GM12878	blood:	n/a	n/a
16	BCL11A	chr7:101934677-101935276	GM12878	blood:	n/a	chr7:101934935-101934944
17	BCL3	chr7:101934706-101935237	GM12878	blood:	n/a	chr7:101934935-101934944
18	BCLAF1	chr7:101932078-101932752	GM12878	blood:	n/a	chr7:101932316-101932325
19	BCLAF1	chr7:101934439-101935371	GM12878	blood:	n/a	chr7:101934935-101934944
20	BCLAF1	chr7:101934466-101935271	GM12878	blood:	n/a	chr7:101934935-101934944
21	BHLHE40	chr7:101927982-101928018	K562	blood:	n/a	n/a
22	BHLHE40	chr7:101922753-101923087	GM12878	blood:	n/a	chr7:101923056-101923072 chr7:101923050-101923066
23	BHLHE40	chr7:101922115-101922233	GM12878	blood:	n/a	n/a
24	BHLHE40	chr7:101922853-101923135	K562	blood:	n/a	chr7:101923056-101923072 chr7:101923050-101923066
25	BHLHE40	chr7:101927712-101928121	GM12878	blood:	n/a	n/a
26	BHLHE40	chr7:101929495-101929593	GM12878	blood:	n/a	n/a
27	BHLHE40	chr7:101934687-101935239	GM12878	blood:	n/a	n/a
28	BHLHE40	chr7:101930201-101930310	K562	blood:	n/a	n/a
29	BHLHE40	chr7:101930107-101930614	GM12878	blood:	n/a	chr7:101930365-101930381
30	BRCA1	chr7:101930871-101930876	Hela-S3	cervix:	n/a	n/a
31	BRCA1	chr7:101930490-101930573	GM12878	blood:	n/a	n/a
32	BRCA1	chr7:101929779-101929787	Hela-S3	cervix:	n/a	n/a
33	CBX3	chr7:101930109-101930402	K562	blood:	n/a	n/a
34	CBX3	chr7:101929398-101929943	K562	blood:	n/a	n/a
35	CBX3	chr7:101933049-101933338	K562	blood:	n/a	n/a
36	CBX3	chr7:101933036-101933344	K562	blood:	n/a	n/a
37	CCNT2	chr7:101922897-101923118	K562	blood:	n/a	n/a
38	CCNT2	chr7:101929388-101930765	K562	blood:	n/a	chr7:101929765-101929774 chr7:101930660-101930669 chr7:101930021-101930030
39	CEBPB	chr7:101934485-101934750	HepG2	liver:	n/a	n/a
40	CEBPB	chr7:101929446-101929820	A549	lung:	n/a	n/a
41	CEBPB	chr7:101929431-101929985	HepG2	liver:	n/a	n/a
42	CEBPB	chr7:101934672-101935291	GM12878	blood:	n/a	n/a
43	CEBPB	chr7:101929485-101929756	HepG2	liver:	n/a	n/a
44	CEBPB	chr7:101922834-101923034	H1-hESC	embryonic stem cell:	n/a	n/a
45	CEBPB	chr7:101929427-101929955	K562	blood:	n/a	n/a
46	CEBPB	chr7:101934541-101934677	K562	blood:	n/a	n/a
47	CEBPB	chr7:101929289-101930001	MCF-7	breast:	n/a	n/a
48	CEBPB	chr7:101929314-101930057	A549	lung:	n/a	n/a
49	CEBPB	chr7:101929317-101929913	K562	blood:	n/a	n/a
50	CEBPB	chr7:101929254-101929994	MCF-7	breast:	n/a	n/a

(count:1283 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:101923726-101923776	SKMC	muscle:	n/a
2	chr7:101936318-101936368	MCF10A-Er-Src	breast:	n/a
3	chr7:101923726-101923776	SKMC	muscle:	n/a
4	chr7:101936318-101936368	MCF10A-Er-Src	breast:	n/a
5	chr7:101930855-101930905	HepG2	liver:	n/a
6	chr7:101926568-101926618	HRCEpiC	kidney:	n/a
7	chr7:101931088-101931138	AG04449	skin:	fetal
8	chr7:101936527-101936577	CMK	blood:	n/a
9	chr7:101931088-101931138	AG09309	skin:	n/a
10	chr7:101926568-101926618	AG09319	gingival:	n/a
11	chr7:101934892-101934942	HRCEpiC	kidney:	n/a
12	chr7:101936362-101936412	A549	lung:	n/a
13	chr7:101938115-101938165	AG09319	gingival:	n/a
14	chr7:101931088-101931138	IMR90	lung:	fetal
15	chr7:101926568-101926618	HRPEpiC	eye:	n/a
16	chr7:101928206-101928256	NHDF-neo	bronchial:	n/a
17	chr7:101936362-101936412	GM12878	blood:	n/a
18	chr7:101934892-101934942	HRE	kidney:	n/a
19	chr7:101927973-101928023	HPAEpiC	pulmonary alveolar:	n/a
20	chr7:101928206-101928256	HCM	heart:	n/a
21	chr7:101930855-101930905	A549	lung:	n/a
22	chr7:101934892-101934942	HIPEpiC	eye:	n/a
23	chr7:101930366-101930416	NH-A	brain:	n/a
24	chr7:101934892-101934942	HepG2	liver:	n/a
25	chr7:101936362-101936412	LNCaP	prostate:	n/a
26	chr7:101930855-101930905	SK-N-MC	brain:	n/a
27	chr7:101936230-101936280	PANC-1	pancreas:	n/a
28	chr7:101936527-101936577	HepG2	liver:	n/a
29	chr7:101927904-101927954	HEEpiC	esophagus:	n/a
30	chr7:101936430-101936480	ECC-1	luminal epithelium:	n/a
31	chr7:101922985-101923035	HUVEC	blood vessel:	n/a
32	chr7:101936230-101936280	SK-N-SH	brain:	n/a
33	chr7:101922985-101923035	HMEC	breast:	n/a
34	chr7:101923726-101923776	HL-60	blood:	n/a
35	chr7:101928560-101928610	MCF10A-Er-Src	breast:	n/a
36	chr7:101930366-101930416	SK-N-MC	brain:	n/a
37	chr7:101936230-101936280	ProgFib	skin:	n/a
38	chr7:101936362-101936412	HNPCEpiC	eye:	n/a
39	chr7:101929626-101929676	SAEC	small airway:	n/a
40	chr7:101936362-101936412	NH-A	brain:	n/a
41	chr7:101932902-101932952	HCM	heart:	n/a
42	chr7:101930855-101930905	Caco-2	colon:	n/a
43	chr7:101927904-101927954	HepG2	liver:	n/a
44	chr7:101931088-101931138	NB4	blood:	n/a
45	chr7:101936362-101936412	T-47D	breast:	n/a
46	chr7:101936527-101936577	HUVEC	blood vessel:	n/a
47	chr7:101932902-101932952	PFSK-1	brain:	n/a
48	chr7:101932902-101932952	ECC-1	luminal epithelium:	n/a
49	chr7:101934892-101934942	SK-N-SH	brain:	n/a
50	chr7:101931734-101931784	NH-A	brain:	n/a

(count:79 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr7:101922803..101925073-chr7:102029717..102032176,2	K562	blood:
2	chr7:101933755..101935437-chr7:101946466..101948365,2	K562	blood:
3	chr7:101921891..101926717-chr7:102108345..102112477,4	MCF-7	breast:
4	chr7:101913664..101916452-chr7:101928530..101931361,3	MCF-7	breast:
5	chr7:101928787..101931103-chr7:102068697..102071521,3	MCF-7	breast:
6	chr7:101928479..101930967-chr7:101967385..101968999,2	MCF-7	breast:
7	chr3:25824746..25825695-chr7:101929432..101929994,2	Hela-S3	cervix:
8	chr7:101922445..101923602-chr7:102030821..102031873,18	MCF-7	breast:
9	chr7:101922960..101924635-chr7:102029793..102032435,2	MCF-7	breast:
10	chr7:101928063..101931419-chr7:102036448..102039604,3	K562	blood:
11	chr7:101922722..101923289-chr7:102036073..102036657,2	MCF-7	breast:
12	chr7:101168305..101170280-chr7:101929643..101931645,2	K562	blood:
13	chr7:101930945..101933458-chr7:101949436..101952380,2	K562	blood:
14	chr7:101929055..101931888-chr7:101946195..101949468,3	MCF-7	breast:
15	chr7:101930001..101933436-chr7:101942768..101945617,4	MCF-7	breast:
16	chr7:101928656..101931104-chr7:102073505..102075200,3	MCF-7	breast:
17	chr7:101922927..101925086-chr7:101959740..101962497,2	K562	blood:
18	chr7:101929481..101931029-chr7:101947545..101949971,2	MCF-7	breast:
19	chr7:101929851..101931493-chr7:102106221..102107741,2	MCF-7	breast:
20	chr5:139486844..139487633-chr7:101929656..101930297,2	Hela-S3	cervix:
21	chr7:101931067..101932687-chr7:101942906..101945348,2	MCF-7	breast:
22	chr7:101928798..101932445-chr7:101950032..101952249,4	MCF-7	breast:
23	chr7:101928402..101930093-chr7:102073347..102075211,2	K562	blood:
24	chr5:11784634..11787064-chr7:101928617..101931405,2	MCF-7	breast:
25	chr7:101929484..101930470-chr9:115983303..115983803,2	MCF-7	breast:
26	chr7:101921316..101924542-chr7:102043674..102045753,3	MCF-7	breast:
27	chr7:101922644..101923376-chr7:102090423..102091348,2	MCF-7	breast:
28	chr7:101914536..101919891-chr7:101927361..101932016,8	MCF-7	breast:
29	chr7:101927893..101931251-chr7:102072337..102075849,4	MCF-7	breast:
30	chr7:101928482..101930196-chr7:102103795..102105466,2	MCF-7	breast:
31	chr7:101929651..101930349-chr8:142425451..142425971,2	HCT-116	colon:
32	chr7:101929723..101930292-chr9:115983304..115983823,2	MCF-7	breast:
33	chr7:101924860..101932400-chr7:102029531..102038487,21	MCF-7	breast:
34	chr7:101929371..101932604-chr7:101956316..101959591,3	MCF-7	breast:
35	chr7:101931459..101933316-chr7:102074143..102076023,2	K562	blood:
36	chr7:101933934..101936298-chr7:101951581..101953703,2	MCF-7	breast:
37	chr2:62932638..62933327-chr7:101929432..101930129,2	Hela-S3	cervix:
38	chr7:101928285..101931151-chr7:101931936..101935513,3	K562	blood:
39	chr7:101922653..101924580-chr7:101925750..101927618,2	K562	blood:
40	chr7:101931480..101934447-chr7:101940162..101942129,3	MCF-7	breast:
41	chr7:101921464..101924386-chr7:102034255..102038288,3	MCF-7	breast:
42	chr7:101933901..101936240-chr7:101942791..101945477,2	MCF-7	breast:
43	chr7:101935058..101937626-chr7:102103527..102105838,2	MCF-7	breast:
44	chr7:101935291..101937717-chr7:101943304..101946108,2	K562	blood:
45	chr2:38977978..38978650-chr7:101929677..101930517,2	Hela-S3	cervix:
46	chr7:101937279..101939356-chr7:102035077..102036831,2	MCF-7	breast:
47	chr7:101929038..101929614-chr7:102030921..102031723,2	MCF-7	breast:
48	chr7:101457570..101460867-chr7:101928374..101931760,6	MCF-7	breast:
49	chr16:74734498..74735318-chr7:101929629..101930391,2	Hela-S3	cervix:
50	chr7:101921111..101923633-chr7:101957670..101959670,2	MCF-7	breast:

No data

miRNA name	Chromosome Location	mirBase accession
hsa-miR-4285	chr7:101936379-101936396	MIMAT0016913

No data

Variant related genes	Relation type
SH2B2	TF binding region
MIR4285	TF binding region
SH2B2	CpG island
MIR4285	CpG island
ENSG00000119321	chromatin interactions
ENSG00000152944	chromatin interactions
ENSG00000136868	chromatin interactions
ENSG00000212195	chromatin interactions
ENSG00000245146	chromatin interactions
ENSG00000151092	chromatin interactions
ENSG00000160993	chromatin interactions
ENSG00000185129	chromatin interactions
ENSG00000239969	chromatin interactions
ENSG00000160999	chromatin interactions
ENSG00000264471	chromatin interactions
ENSG00000260430	chromatin interactions
ENSG00000161036	chromatin interactions
ENSG00000059804	chromatin interactions
ENSG00000115875	chromatin interactions
ENSG00000257923	chromatin interactions
ENSG00000115504	chromatin interactions
ENSG00000128563	chromatin interactions
ENSG00000239480	chromatin interactions
ENSG00000168404	chromatin interactions
ENSG00000239486	chromatin interactions
ENSG00000160991	chromatin interactions

Extended variants
information (count: 845 )
Associated
traits (count: 94 )

Variant overlapped rSNPs/rCNVs (count:845 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2230103	chr7:101921289-101921290	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs118010189	chr7:101921292-101921293	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs373393100	chr7:101921315-101921316	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs144393643	chr7:101921334-101921335	Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs148760130	chr7:101921335-101921336	Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs372364721	chr7:101921372-101921373	Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs375054514	chr7:101921375-101921376	Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs202079615	chr7:101921377-101921378	Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs369617020	chr7:101921383-101921384	Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs76291147	chr7:101921413-101921414	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs562778935	chr7:101921418-101921419	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs377165504	chr7:101921472-101921473	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs533297576	chr7:101921485-101921486	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs551724504	chr7:101921520-101921521	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs803086	chr7:101921522-101921523	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs533989074	chr7:101921539-101921540	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs547064345	chr7:101921544-101921545	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs370354726	chr7:101921557-101921558	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs535820565	chr7:101921589-101921590	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs557112572	chr7:101921626-101921627	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs183330153	chr7:101921635-101921636	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs570466001	chr7:101921643-101921644	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs58887432	chr7:101921690-101921691	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs186964513	chr7:101921694-101921695	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs376977365	chr7:101921719-101921720	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs138157548	chr7:101921720-101921721	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs535419068	chr7:101921777-101921778	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs189747882	chr7:101921778-101921779	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs573679340	chr7:101921794-101921795	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs547219644	chr7:101921812-101921813	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs56132647	chr7:101921851-101921852	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs188359696	chr7:101921895-101921896	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs201139444	chr7:101921931-101921932	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs112803681	chr7:101921938-101921939	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs28414936	chr7:101921945-101921946	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs28433949	chr7:101921948-101921949	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs587699006	chr7:101921949-101921950	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs71559451	chr7:101921952-101921953	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs201062424	chr7:101922063-101922064	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs560476448	chr7:101922104-101922105	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs192546920	chr7:101922105-101922106	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs185327986	chr7:101922115-101922116	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs539118779	chr7:101922123-101922124	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs111346629	chr7:101922159-101922160	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs535546105	chr7:101922197-101922198	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs557549056	chr7:101922203-101922204	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs575806854	chr7:101922206-101922207	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs536980088	chr7:101922228-101922229	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs551077099	chr7:101922353-101922354	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs568864581	chr7:101922387-101922388	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:94)

Disease	PMID	Source
Basal cell lymphoma	17170743	CNVD
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
Non-small cell lung cancer	21829676	CNVD
Gastric cancer	24379144	CNVD
Glioblastoma multiforme	17002787	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Lissencephaly	21572526	CNVD
Breast cancer	17603634	CNVD
Liposarcoma	21253554	CNVD
Breast cancer	16397240	CNVD
Acute myeloid leukemia	16864856	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
small cell lung cancer	20016488	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
Prostate cancer	16461572	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Burkitt''s lymphoma	19759907	CNVD
Malignant melanoma	17260012	CNVD
Myelodysplastic syndrome	21251322	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	21785460	CNVD
Chronic myeloid leukemia	21384125	CNVD
Bladder cancer	21909424	CNVD
Biliary cancer	19435499	CNVD
Myelofibrosis	22110671	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	16608533	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Liver carcinoma	19366792	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Adenocarcinoma	19607727	CNVD
Multiple myeloma	16461302	CNVD
Breast cancer	21858162	CNVD
Emphysema	19352772	CNVD
Effusion lymphoma	18079361	CNVD
Medulloblastoma	17653508	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Autism	19401682	CNVD
Neuroticism	17667963	CNVD
Prostate cancer	18632612	CNVD
Urothelial carcinoma	21177765	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Breast cancer	21364760	CNVD
Cancer	19907438	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Breast cancer	21509527	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
Breast cancer	22522925	CNVD
Cancer	20164919	CNVD
Congenital anomalies of the kidney and urinary tract	18316590	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:1160 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:101892800-101928000	Weak transcription	Esophagus	oesophagus
2	chr7:101892800-101928400	Weak transcription	Right Ventricle	heart
3	chr7:101897600-101928000	Weak transcription	Primary T cells from cord blood	blood
4	chr7:101898000-101928200	Weak transcription	Stomach Smooth Muscle	stomach
5	chr7:101898200-101922600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
6	chr7:101899800-101922800	Weak transcription	Right Atrium	heart
7	chr7:101904600-101922800	Weak transcription	Colon Smooth Muscle	Colon
8	chr7:101904600-101928200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
9	chr7:101908000-101929200	Weak transcription	Gastric	stomach
10	chr7:101908400-101922600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
11	chr7:101910200-101928400	Weak transcription	Liver	Liver
12	chr7:101912200-101922600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr7:101912400-101922600	Weak transcription	Fetal Thymus	thymus
14	chr7:101914200-101923000	Weak transcription	Fetal Brain Female	brain
15	chr7:101914400-101923000	Weak transcription	Brain Hippocampus Middle	brain
16	chr7:101915600-101922600	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
17	chr7:101915600-101922600	Weak transcription	Skeletal Muscle Male	skeletal muscle
18	chr7:101915600-101922800	Weak transcription	Adipose Nuclei	Adipose
19	chr7:101915600-101923000	Weak transcription	HUES6 Cell Line	embryonic stem cell
20	chr7:101915600-101923000	Weak transcription	Brain Cingulate Gyrus	brain
21	chr7:101915800-101928000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
22	chr7:101915800-101929000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
23	chr7:101916000-101922600	Weak transcription	Fetal Muscle Leg	muscle
24	chr7:101916000-101922600	Weak transcription	Placenta	Placenta
25	chr7:101916000-101922600	Weak transcription	Skeletal Muscle Female	skeletal muscle
26	chr7:101916000-101924800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
27	chr7:101917400-101922600	Weak transcription	Fetal Muscle Trunk	muscle
28	chr7:101917400-101929400	Weak transcription	HMEC	breast
29	chr7:101917600-101922600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
30	chr7:101917600-101922600	Weak transcription	HSMM	muscle
31	chr7:101917600-101923000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
32	chr7:101917600-101923000	Weak transcription	K562	blood
33	chr7:101917600-101928000	Weak transcription	Colonic Mucosa	Colon
34	chr7:101917800-101922600	Weak transcription	A549	lung
35	chr7:101917800-101922800	Weak transcription	Rectal Mucosa Donor 31	rectum
36	chr7:101917800-101923000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
37	chr7:101917800-101923000	Weak transcription	Placenta Amnion	Placenta Amnion
38	chr7:101918000-101922600	Weak transcription	HepG2	liver
39	chr7:101918000-101922800	Weak transcription	Fetal Intestine Large	intestine
40	chr7:101918200-101922600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
41	chr7:101918200-101922600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
42	chr7:101918200-101922600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
43	chr7:101918600-101922600	Weak transcription	Duodenum Mucosa	Duodenum
44	chr7:101918800-101929000	Weak transcription	Stomach Mucosa	stomach
45	chr7:101919000-101922600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
46	chr7:101919000-101922600	Weak transcription	Fetal Intestine Small	intestine
47	chr7:101919000-101922600	Weak transcription	Fetal Stomach	stomach
48	chr7:101919000-101928200	Weak transcription	Lung	lung
49	chr7:101920000-101922600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
50	chr7:101920600-101922600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung

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