Variant report

Variant	nsv539029
Chromosome Location	chr7:96749866-96850819
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:809)
CpG islands
(count:246)
Chromatin interactive
region (count:71)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:809 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:96758215-96758225	K562	blood:	n/a	n/a
2	ARID3A	chr7:96755990-96756047	K562	blood:	n/a	n/a
3	ARID3A	chr7:96774381-96774695	HepG2	liver:	n/a	n/a
4	ARID3A	chr7:96827708-96828274	K562	blood:	n/a	n/a
5	ARID3A	chr7:96808791-96809102	K562	blood:	n/a	n/a
6	ARID3A	chr7:96808875-96809032	HepG2	liver:	n/a	n/a
7	ARID3A	chr7:96750393-96750727	K562	blood:	n/a	n/a
8	ARID3A	chr7:96763215-96763471	HepG2	liver:	n/a	n/a
9	ARID3A	chr7:96774354-96774703	K562	blood:	n/a	n/a
10	ATF1	chr7:96827959-96828206	K562	blood:	n/a	n/a
11	ATF1	chr7:96755793-96756101	K562	blood:	n/a	n/a
12	ATF3	chr7:96759761-96760043	K562	blood:	n/a	n/a
13	ATF3	chr7:96755798-96756175	K562	blood:	n/a	n/a
14	ATF3	chr7:96755837-96756175	K562	blood:	n/a	n/a
15	BACH1	chr7:96755802-96756103	H1-hESC	embryonic stem cell:	n/a	n/a
16	BACH1	chr7:96807240-96807249	K562	blood:	n/a	n/a
17	BACH1	chr7:96755845-96756129	K562	blood:	n/a	n/a
18	BACH1	chr7:96759823-96759861	K562	blood:	n/a	n/a
19	BACH1	chr7:96831647-96831728	H1-hESC	embryonic stem cell:	n/a	n/a
20	BHLHE40	chr7:96751953-96752089	K562	blood:	n/a	n/a
21	BHLHE40	chr7:96827790-96827857	K562	blood:	n/a	n/a
22	BHLHE40	chr7:96759739-96760464	K562	blood:	n/a	chr7:96759808-96759824
23	BHLHE40	chr7:96774566-96774587	GM12878	blood:	n/a	n/a
24	BHLHE40	chr7:96845068-96845175	K562	blood:	n/a	n/a
25	BHLHE40	chr7:96808945-96808968	K562	blood:	n/a	n/a
26	BHLHE40	chr7:96755834-96756513	K562	blood:	n/a	n/a
27	CBX3	chr7:96755668-96756204	K562	blood:	n/a	n/a
28	CBX3	chr7:96770772-96771281	K562	blood:	n/a	n/a
29	CBX3	chr7:96768250-96769041	K562	blood:	n/a	n/a
30	CBX3	chr7:96759741-96760182	K562	blood:	n/a	n/a
31	CBX3	chr7:96759642-96760433	K562	blood:	n/a	n/a
32	CBX3	chr7:96770298-96770477	K562	blood:	n/a	n/a
33	CBX3	chr7:96768373-96768762	K562	blood:	n/a	n/a
34	CBX3	chr7:96770179-96770629	K562	blood:	n/a	n/a
35	CCNT2	chr7:96844963-96845163	K562	blood:	n/a	n/a
36	CCNT2	chr7:96756424-96756624	K562	blood:	n/a	n/a
37	CCNT2	chr7:96827772-96828272	K562	blood:	n/a	n/a
38	CEBPB	chr7:96808820-96808988	K562	blood:	n/a	n/a
39	CEBPB	chr7:96756171-96756612	K562	blood:	n/a	n/a
40	CEBPB	chr7:96831286-96831570	HepG2	liver:	n/a	n/a
41	CEBPB	chr7:96827982-96828289	K562	blood:	n/a	n/a
42	CEBPB	chr7:96803699-96803935	IMR90	lung:	n/a	n/a
43	CEBPB	chr7:96795410-96795696	H1-hESC	embryonic stem cell:	n/a	n/a
44	CEBPB	chr7:96776066-96776260	H1-hESC	embryonic stem cell:	n/a	n/a
45	CEBPB	chr7:96755968-96755974	K562	blood:	n/a	n/a
46	CEBPB	chr7:96756219-96756598	K562	blood:	n/a	n/a
47	CEBPB	chr7:96795414-96795693	K562	blood:	n/a	n/a
48	CEBPB	chr7:96771220-96771438	H1-hESC	embryonic stem cell:	n/a	chr7:96771323-96771334
49	CEBPB	chr7:96793675-96793788	K562	blood:	n/a	n/a
50	CEBPD	chr7:96755684-96756177	K562	blood:	n/a	n/a

(count:246 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:96770912-96770962	A549	lung:	n/a
2	chr7:96789745-96789795	BE2_C	brain:	n/a
3	chr7:96770912-96770962	A549	lung:	n/a
4	chr7:96789745-96789795	BE2_C	brain:	n/a
5	chr7:96770912-96770962	RPTEC	kidney:	n/a
6	chr7:96762818-96762868	HepG2	liver:	n/a
7	chr7:96762818-96762868	GM12878	blood:	n/a
8	chr7:96789745-96789795	H1-hESC	embryonic stem cell:	embryo
9	chr7:96762818-96762868	HUVEC	blood vessel:	n/a
10	chr7:96762818-96762868	GM19239	blood:	n/a
11	chr7:96770912-96770962	NH-A	brain:	n/a
12	chr7:96770912-96770962	HCT-116	colon:	n/a
13	chr7:96789745-96789795	NT2-D1	testis:	n/a
14	chr7:96762818-96762868	HPAEpiC	pulmonary alveolar:	n/a
15	chr7:96789745-96789795	SAEC	small airway:	n/a
16	chr7:96762818-96762868	LNCaP	prostate:	n/a
17	chr7:96770912-96770962	NHBE	bronchial:	n/a
18	chr7:96770912-96770962	SK-N-SH_RA	brain:	n/a
19	chr7:96770912-96770962	HCF	heart:	n/a
20	chr7:96789745-96789795	K562	blood:	n/a
21	chr7:96770912-96770962	GM12878	blood:	n/a
22	chr7:96789745-96789795	PANC-1	pancreas:	n/a
23	chr7:96770912-96770962	HUVEC	blood vessel:	n/a
24	chr7:96770912-96770962	HPAEpiC	pulmonary alveolar:	n/a
25	chr7:96750500-96750550	HPAEpiC	pulmonary alveolar:	n/a
26	chr7:96750500-96750550	NHDF-neo	bronchial:	n/a
27	chr7:96750500-96750550	GM12891	blood:	n/a
28	chr7:96750500-96750550	SK-N-SH	brain:	n/a
29	chr7:96789745-96789795	IMR90	lung:	fetal
30	chr7:96750500-96750550	MCF10A-Er-Src	breast:	n/a
31	chr7:96789745-96789795	AoSMC	blood vessel:	n/a
32	chr7:96789745-96789795	NHDF-neo	bronchial:	n/a
33	chr7:96789745-96789795	HEEpiC	esophagus:	n/a
34	chr7:96789745-96789795	NHBE	bronchial:	n/a
35	chr7:96770912-96770962	HNPCEpiC	eye:	n/a
36	chr7:96750500-96750550	HEK293	kidney:	embryo
37	chr7:96762818-96762868	AG09319	gingival:	n/a
38	chr7:96770912-96770962	PFSK-1	brain:	n/a
39	chr7:96762818-96762868	AG04450	lung:	fetal
40	chr7:96770912-96770962	CMK	blood:	n/a
41	chr7:96789745-96789795	AG04449	skin:	fetal
42	chr7:96762818-96762868	HMEC	breast:	n/a
43	chr7:96770912-96770962	HL-60	blood:	n/a
44	chr7:96770912-96770962	Jurkat	blood:	n/a
45	chr7:96789745-96789795	GM19239	blood:	n/a
46	chr7:96770912-96770962	H1-hESC	embryonic stem cell:	embryo
47	chr7:96762818-96762868	ECC-1	luminal epithelium:	n/a
48	chr7:96750500-96750550	HRCEpiC	kidney:	n/a
49	chr7:96750500-96750550	CMK	blood:	n/a
50	chr7:96750500-96750550	HRPEpiC	eye:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr7:96752164..96755225-chr7:96755419..96757960,4	K562	blood:
2	chr7:96774472..96776990-chr7:96778997..96783154,4	K562	blood:
3	chr7:96774660..96775254-chr7:96808529..96809221,2	MCF-7	breast:
4	chr7:96748725..96750557-chr7:96827125..96829431,2	K562	blood:
5	chr7:96815488..96818084-chr7:96818414..96821704,4	K562	blood:
6	chr7:96802770..96806214-chr7:96807512..96809959,3	K562	blood:
7	chr7:96761601..96763207-chr7:96781480..96783225,2	K562	blood:
8	chr7:96759320..96762416-chr7:96764442..96769272,6	K562	blood:
9	chr7:96774346..96775064-chr7:97011084..97011839,3	MCF-7	breast:
10	chr7:96765006..96767658-chr7:96799778..96802504,2	K562	blood:
11	chr7:96791280..96793153-chr7:96799755..96801973,2	K562	blood:
12	chr7:96806850..96809005-chr7:97600117..97602483,2	MCF-7	breast:
13	chr7:96747720..96750174-chr7:96767579..96769561,2	K562	blood:
14	chr7:96722317..96724979-chr7:96765637..96768618,2	MCF-7	breast:
15	chr7:96746815..96748527-chr7:96774401..96776566,2	K562	blood:
16	chr7:96767307..96769566-chr7:96804209..96806523,2	K562	blood:
17	chr7:96784450..96786338-chr7:96788596..96790706,2	K562	blood:
18	chr7:96794189..96796264-chr7:96799436..96802402,4	K562	blood:
19	chr7:96774152..96774968-chr7:96808489..96809426,2	K562	blood:
20	chr7:96801538..96803188-chr7:96810156..96813004,2	K562	blood:
21	chr7:96761601..96763207-chr7:96781480..96783225,2	K562	blood:
22	chr7:96733723..96734557-chr7:96808564..96809069,3	MCF-7	breast:
23	chr7:96815194..96818084-chr7:96819394..96821737,4	K562	blood:
24	chr7:96756033..96757904-chr7:96764300..96767170,3	K562	blood:
25	chr7:96755308..96757076-chr7:96769182..96771029,2	K562	blood:
26	chr7:96748869..96751979-chr7:96758718..96762589,5	K562	blood:
27	chr7:96774113..96775121-chr7:97464719..97465350,5	MCF-7	breast:
28	chr7:96748869..96751979-chr7:96758718..96762589,5	K562	blood:
29	chr7:96767307..96769566-chr7:96804209..96806523,2	K562	blood:
30	chr7:96779781..96781668-chr7:96787687..96790024,2	K562	blood:
31	chr11:65266389..65266952-chr7:96765475..96765975,2	Hela-S3	cervix:
32	chr7:96755308..96757076-chr7:96769182..96771029,2	K562	blood:
33	chr7:96745635..96748497-chr7:96798834..96800388,2	K562	blood:
34	chr7:96733720..96734656-chr7:96808486..96809428,8	K562	blood:
35	chr7:96791280..96793153-chr7:96799755..96801973,2	K562	blood:
36	chr7:96775014..96778181-chr7:96779788..96783154,4	K562	blood:
37	chr7:96779781..96781668-chr7:96787687..96790024,2	K562	blood:
38	chr7:96775014..96778181-chr7:96779788..96783154,4	K562	blood:
39	chr7:96756335..96758399-chr7:96773893..96776868,2	K562	blood:
40	chr7:96756335..96758399-chr7:96773893..96776868,2	K562	blood:
41	chr7:96774088..96774631-chr7:96808530..96809389,2	MCF-7	breast:
42	chr7:96815194..96818084-chr7:96819394..96821737,4	K562	blood:
43	chr7:96745279..96751948-chr7:96754118..96758350,11	K562	blood:
44	chr7:96802770..96806214-chr7:96807512..96809959,3	K562	blood:
45	chr7:96815072..96817361-chr7:96821955..96824089,2	K562	blood:
46	chr7:96757705..96760493-chr7:96778782..96780656,2	K562	blood:
47	chr7:96759570..96761270-chr7:96764442..96766982,2	K562	blood:
48	chr7:96757705..96760493-chr7:96778782..96780656,2	K562	blood:
49	chr7:96733732..96734563-chr7:96808460..96809316,2	MCF-7	breast:
50	chr7:96746484..96749915-chr7:96785838..96788939,4	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-DLX5-5	chr7:96764327-96764873	NONHSAT122140
2	lnc-DLX6-2	chr7:96771985-96772147	NONHSAT122139

No data

Variant related genes	Relation type
HMGB3P21	TF binding region
ACN9	TF binding region
ENSG00000224475	TF binding region
HMGB3P21	CpG island
ACN9	CpG island
ENSG00000224475	CpG island
ENSG00000251562	chromatin interactions
ENSG00000243554	chromatin interactions
ENSG00000196636	chromatin interactions
ENSG00000224551	chromatin interactions

Extended variants
information (count: 3228 )
Associated
traits (count: 80 )

Variant overlapped rSNPs/rCNVs (count:3228 , 50 per page) page: 1 2 3 4 5 6 7 ... 65

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs185611435	chr7:96749901-96749902	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
2	rs190517146	chr7:96749906-96749907	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs577041773	chr7:96749951-96749952	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs539757364	chr7:96749960-96749961	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs536659323	chr7:96749965-96749966	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs539500501	chr7:96749979-96749980	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs556051610	chr7:96750007-96750008	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs28693735	chr7:96750011-96750012	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs181607458	chr7:96750016-96750017	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs555055426	chr7:96750037-96750038	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs147732756	chr7:96750067-96750068	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs571851034	chr7:96750102-96750103	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs540669228	chr7:96750134-96750135	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs78854657	chr7:96750141-96750142	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs573903652	chr7:96750145-96750146	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs373155048	chr7:96750180-96750181	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs532677205	chr7:96750227-96750228	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs185930791	chr7:96750234-96750235	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs151110846	chr7:96750257-96750258	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs531944421	chr7:96750265-96750266	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs188826219	chr7:96750341-96750342	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs568556496	chr7:96750356-96750357	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs527815532	chr7:96750401-96750402	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs143984542	chr7:96750404-96750405	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs146410484	chr7:96750441-96750442	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs140804517	chr7:96750455-96750456	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs144643411	chr7:96750466-96750467	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs73708859	chr7:96750473-96750474	Weak transcription Enhancers Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs181262298	chr7:96750487-96750488	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs145520555	chr7:96750525-96750526	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs555192221	chr7:96750575-96750576	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs571784250	chr7:96750652-96750653	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs559158704	chr7:96750711-96750712	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs13226221	chr7:96750712-96750713	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs186189673	chr7:96750721-96750722	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs557433337	chr7:96750808-96750809	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs577586302	chr7:96750829-96750830	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs531369213	chr7:96750838-96750839	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs148871986	chr7:96750864-96750865	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs563183286	chr7:96750878-96750879	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs528154074	chr7:96750882-96750883	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs13239188	chr7:96750897-96750898	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs544743146	chr7:96750918-96750919	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs532084381	chr7:96750924-96750925	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs369976120	chr7:96750955-96750956	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs190850642	chr7:96751004-96751005	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs553831217	chr7:96751064-96751065	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs60114973	chr7:96751084-96751085	Weak transcription Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs7789931	chr7:96751120-96751121	Weak transcription Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs182711356	chr7:96751152-96751153	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:80)

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
Stenocardia	21860640	CNVD
Vasospasm	21860640	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
Glioblastoma multiforme	21750150	CNVD
Cancer	21183584	CNVD
Hepatocellular carcinoma	16750200	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
Metanephric adenoma	20802469	CNVD
abortions and stillbirths	19751515	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Acute myeloid leukemia	20729466	CNVD
Lung cancer	18438408	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Schizophrenia	17879154	CNVD
Prostate cancer	16573809	CNVD
Prostate cancer	16461572	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Autism	20858243	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Burkitt''s lymphoma	19759907	CNVD
Malignant melanoma	17260012	CNVD
Myoclonus-dystonia	17898012	CNVD
Myelodysplastic syndrome	21251322	CNVD
Cancer	20164920	CNVD
abnormal development	18461090	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	21785460	CNVD
Myelofibrosis	22110671	CNVD
Prostate cancer	22341455	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:728 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:96746800-96751800	Active TSS	K562	blood
2	chr7:96747400-96759800	Weak transcription	Spleen	Spleen
3	chr7:96747600-96753000	Weak transcription	Small Intestine	intestine
4	chr7:96747600-96759000	Weak transcription	Esophagus	oesophagus
5	chr7:96747600-96768200	Weak transcription	Sigmoid Colon	Sigmoid Colon
6	chr7:96747800-96768200	Weak transcription	Aorta	Aorta
7	chr7:96748000-96759000	Weak transcription	Left Ventricle	heart
8	chr7:96748200-96759800	Weak transcription	Fetal Intestine Small	intestine
9	chr7:96748400-96750600	Enhancers	Primary neutrophils fromperipheralblood	blood
10	chr7:96748400-96767200	Weak transcription	Fetal Stomach	stomach
11	chr7:96748400-96768200	Weak transcription	Right Ventricle	heart
12	chr7:96748400-96768400	Weak transcription	Psoas Muscle	Psoas
13	chr7:96748600-96755800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
14	chr7:96748600-96756000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
15	chr7:96748600-96759200	Weak transcription	HMEC	breast
16	chr7:96749000-96750200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
17	chr7:96749000-96750200	Enhancers	HepG2	liver
18	chr7:96749000-96755400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
19	chr7:96749000-96768200	Weak transcription	Right Atrium	heart
20	chr7:96749200-96750400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
21	chr7:96749200-96750600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
22	chr7:96749200-96752000	Weak transcription	Primary T helper cells fromperipheralblood	blood
23	chr7:96749200-96752800	Weak transcription	Fetal Kidney	kidney
24	chr7:96749200-96755800	Weak transcription	HUES64 Cell Line	embryonic stem cell
25	chr7:96749200-96759800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
26	chr7:96749200-96768000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
27	chr7:96749400-96750200	Enhancers	Dnd41	blood
28	chr7:96749400-96750400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
29	chr7:96749400-96751800	Weak transcription	HUES48 Cell Line	embryonic stem cell
30	chr7:96749400-96755600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
31	chr7:96749400-96768000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
32	chr7:96749400-96768200	Weak transcription	Primary T cells from cord blood	blood
33	chr7:96750200-96752000	Weak transcription	Dnd41	blood
34	chr7:96750400-96750600	Enhancers	Primary T killer memory cells from peripheral blood	blood
35	chr7:96750400-96750600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
36	chr7:96750600-96750800	Enhancers	Primary hematopoietic stem cells short term culture	blood
37	chr7:96751800-96752200	Flanking Active TSS	K562	blood
38	chr7:96751800-96752400	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
39	chr7:96752200-96754800	Weak transcription	K562	blood
40	chr7:96752400-96766000	Weak transcription	HUES48 Cell Line	embryonic stem cell
41	chr7:96753600-96759000	Weak transcription	Primary T cells fromperipheralblood	blood
42	chr7:96754800-96755200	Enhancers	K562	blood
43	chr7:96755000-96756600	Enhancers	iPS-15b Cell Line	embryonic stem cell
44	chr7:96755000-96766800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
45	chr7:96755000-96768000	Weak transcription	Adipose Nuclei	Adipose
46	chr7:96755200-96755800	Enhancers	iPS-18 Cell Line	embryonic stem cell
47	chr7:96755200-96755800	Flanking Active TSS	K562	blood
48	chr7:96755200-96756400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
49	chr7:96755400-96755600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
50	chr7:96755400-96755600	Enhancers	HUES6 Cell Line	embryonic stem cell

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