Variant report

Variant	nsv539065
Chromosome Location	chr7:110839832-111194657
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2693)
CpG islands
(count:305)
Chromatin interactive
region (count:305)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2693 , 50 per page) page: 1 2 3 4 5 6 7 ... 54

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:110966486-110967469	K562	blood:	n/a	n/a
2	ARID3A	chr7:110946747-110946768	K562	blood:	n/a	n/a
3	ARID3A	chr7:110869353-110869485	K562	blood:	n/a	n/a
4	ARID3A	chr7:111077670-111079453	K562	blood:	n/a	chr7:111078420-111078436 chr7:111078560-111078576
5	ARID3A	chr7:110895612-110896118	K562	blood:	n/a	n/a
6	ARID3A	chr7:111114444-111116392	K562	blood:	n/a	chr7:111115784-111115800 chr7:111114896-111114912 chr7:111114897-111114913
7	ARID3A	chr7:111157885-111158000	HepG2	liver:	n/a	n/a
8	ARID3A	chr7:110967767-110967878	K562	blood:	n/a	n/a
9	ARID3A	chr7:111150377-111150555	K562	blood:	n/a	n/a
10	ARID3A	chr7:111100636-111100911	K562	blood:	n/a	chr7:111100841-111100857
11	ARID3A	chr7:111181171-111181430	HepG2	liver:	n/a	n/a
12	ARID3A	chr7:110997534-110997571	K562	blood:	n/a	n/a
13	ARID3A	chr7:110968691-110969273	K562	blood:	n/a	n/a
14	ARID3A	chr7:111021038-111021344	HepG2	liver:	n/a	n/a
15	ARID3A	chr7:111170171-111170509	HepG2	liver:	n/a	n/a
16	ARID3A	chr7:111024781-111024793	K562	blood:	n/a	n/a
17	ARID3A	chr7:111126639-111126960	HepG2	liver:	n/a	n/a
18	ARID3A	chr7:111172220-111172476	K562	blood:	n/a	n/a
19	ARID3A	chr7:111116731-111117824	K562	blood:	n/a	n/a
20	ARID3A	chr7:111099362-111100398	K562	blood:	n/a	n/a
21	ARID3A	chr7:110953154-110953413	K562	blood:	n/a	n/a
22	ARID3A	chr7:111118669-111118974	K562	blood:	n/a	n/a
23	ARID3A	chr7:111008626-111008764	K562	blood:	n/a	n/a
24	ARID3A	chr7:111126348-111127214	K562	blood:	n/a	n/a
25	ARID3A	chr7:110969611-110970170	K562	blood:	n/a	n/a
26	ARID3A	chr7:111064774-111065198	HepG2	liver:	n/a	n/a
27	ARID3A	chr7:110968080-110968421	K562	blood:	n/a	n/a
28	ARID3A	chr7:110863537-110864343	K562	blood:	n/a	chr7:110863547-110863563 chr7:110863548-110863564
29	ATF1	chr7:111115090-111115592	K562	blood:	n/a	n/a
30	ATF1	chr7:111126656-111126990	K562	blood:	n/a	n/a
31	ATF1	chr7:111054516-111054769	K562	blood:	n/a	n/a
32	ATF1	chr7:111012802-111012930	K562	blood:	n/a	n/a
33	ATF1	chr7:110863987-110864363	K562	blood:	n/a	n/a
34	ATF1	chr7:110895660-110895855	K562	blood:	n/a	n/a
35	ATF1	chr7:111116070-111116343	K562	blood:	n/a	n/a
36	ATF1	chr7:111172136-111172453	K562	blood:	n/a	n/a
37	ATF1	chr7:111175451-111175458	K562	blood:	n/a	n/a
38	ATF1	chr7:110889894-110890092	K562	blood:	n/a	n/a
39	ATF1	chr7:111163232-111163327	K562	blood:	n/a	n/a
40	ATF1	chr7:111078600-111078973	K562	blood:	n/a	n/a
41	ATF1	chr7:111139180-111139448	K562	blood:	n/a	n/a
42	ATF2	chr7:111167522-111167997	GM12878	blood:	n/a	n/a
43	ATF2	chr7:111053704-111054218	H1-hESC	embryonic stem cell:	n/a	n/a
44	ATF2	chr7:111167450-111168045	GM12878	blood:	n/a	n/a
45	ATF3	chr7:110872430-110873085	A549	lung:	n/a	n/a
46	ATF3	chr7:111116052-111116358	K562	blood:	n/a	n/a
47	ATF3	chr7:111138963-111139597	A549	lung:	n/a	n/a
48	ATF3	chr7:111078506-111078989	K562	blood:	n/a	n/a
49	ATF3	chr7:111156585-111157142	A549	lung:	n/a	chr7:111156907-111156914 chr7:111156904-111156914 chr7:111156906-111156917 chr7:111156906-111156920 chr7:111156904-111156917 chr7:111156904-111156915
50	ATF3	chr7:111156586-111157138	A549	lung:	n/a	chr7:111156907-111156914 chr7:111156904-111156914 chr7:111156906-111156917 chr7:111156906-111156920 chr7:111156904-111156917 chr7:111156904-111156915

(count:305 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:110879415-110879465	HNPCEpiC	eye:	n/a
2	chr7:111079100-111079150	ovcar-3	ovarian:	n/a
3	chr7:111033064-111033114	SK-N-SH_RA	brain:	n/a
4	chr7:110879415-110879465	CMK	blood:	n/a
5	chr7:110879415-110879465	PrEC	prostate:	n/a
6	chr7:111033064-111033114	U87	brain:	n/a
7	chr7:111086055-111086105	MCF-7	breast:	n/a
8	chr7:111033064-111033114	HCPEpiC	choroid plexus:	n/a
9	chr7:111079100-111079150	H1-hESC	embryonic stem cell:	embryo
10	chr7:111079100-111079150	GM12891	blood:	n/a
11	chr7:111079100-111079150	PrEC	prostate:	n/a
12	chr7:111086055-111086105	ProgFib	skin:	n/a
13	chr7:111079100-111079150	GM06990	blood:	n/a
14	chr7:111079100-111079150	NHBE	bronchial:	n/a
15	chr7:111033064-111033114	HMEC	breast:	n/a
16	chr7:111033064-111033114	BE2_C	brain:	n/a
17	chr7:111033064-111033114	AG09319	gingival:	n/a
18	chr7:111033064-111033114	ProgFib	skin:	n/a
19	chr7:111079100-111079150	HRE	kidney:	n/a
20	chr7:111079100-111079150	SKMC	muscle:	n/a
21	chr7:110906785-110906835	Hela-S3	cervix:	n/a
22	chr7:111033064-111033114	HRCEpiC	kidney:	n/a
23	chr7:110906785-110906835	PANC-1	pancreas:	n/a
24	chr7:110906785-110906835	A549	lung:	n/a
25	chr7:110906785-110906835	T-47D	breast:	n/a
26	chr7:111079100-111079150	AG09319	gingival:	n/a
27	chr7:110906785-110906835	HIPEpiC	eye:	n/a
28	chr7:110879415-110879465	PANC-1	pancreas:	n/a
29	chr7:110906785-110906835	NH-A	brain:	n/a
30	chr7:110906785-110906835	U87	brain:	n/a
31	chr7:110879415-110879465	NH-A	brain:	n/a
32	chr7:110879415-110879465	HAEpiC	amniotic membrane:	n/a
33	chr7:111086055-111086105	AG04450	lung:	fetal
34	chr7:111033064-111033114	SK-N-MC	brain:	n/a
35	chr7:111079100-111079150	SAEC	small airway:	n/a
36	chr7:111079100-111079150	SK-N-SH	brain:	n/a
37	chr7:110906785-110906835	CMK	blood:	n/a
38	chr7:110879415-110879465	GM06990	blood:	n/a
39	chr7:111079100-111079150	GM19239	blood:	n/a
40	chr7:110879415-110879465	NHDF-neo	bronchial:	n/a
41	chr7:111086055-111086105	PANC-1	pancreas:	n/a
42	chr7:111033064-111033114	HCT-116	colon:	n/a
43	chr7:111086055-111086105	NHDF-neo	bronchial:	n/a
44	chr7:110906785-110906835	HRCEpiC	kidney:	n/a
45	chr7:111033064-111033114	NT2-D1	testis:	n/a
46	chr7:110906785-110906835	SAEC	small airway:	n/a
47	chr7:110879415-110879465	NHBE	bronchial:	n/a
48	chr7:111086055-111086105	HCPEpiC	choroid plexus:	n/a
49	chr7:110879415-110879465	HCM	heart:	n/a
50	chr7:111086055-111086105	HEEpiC	esophagus:	n/a

(count:305 , 50 per page) page: 1 2 3 4 5 6 7

No.	Distal block	Cell Line	Cell type
1	chr7:110924432..110926999-chr7:110933691..110937635,4	K562	blood:
2	chr7:110729634..110730189-chr7:110952732..110953606,2	MCF-7	breast:
3	chr7:110941905..110944454-chr7:110944620..110946786,2	K562	blood:
4	chr7:110924808..110925532-chr7:111126328..111127072,2	MCF-7	breast:
5	chr7:110890356..110892390-chr7:110893967..110896589,2	K562	blood:
6	chr7:111111427..111114620-chr7:111124257..111128153,3	K562	blood:
7	chr7:110969503..110970311-chr7:111375483..111376413,3	K562	blood:
8	chr7:110873178..110876028-chr7:110879023..110881102,2	K562	blood:
9	chr7:110985007..110987369-chr7:110994363..110996141,2	K562	blood:
10	chr6:31639869..31641695-chr7:111180406..111182806,2	MCF-7	breast:
11	chr7:111025105..111026879-chr7:111027995..111029881,2	K562	blood:
12	chr7:111075731..111078683-chr7:111110429..111113130,2	K562	blood:
13	chr7:110864193..110867019-chr7:110872692..110875184,2	K562	blood:
14	chr7:111149997..111152577-chr7:111162240..111165050,2	K562	blood:
15	chr7:110924432..110929578-chr7:110932859..110937635,6	K562	blood:
16	chr7:111186407..111189009-chr7:111189104..111191721,2	K562	blood:
17	chr7:110890356..110892390-chr7:110893967..110896589,2	K562	blood:
18	chr7:110985007..110987369-chr7:110994363..110996141,2	K562	blood:
19	chr7:110935982..110938365-chr7:110942817..110944691,2	K562	blood:
20	chr7:111050112..111052168-chr7:111053965..111056674,3	K562	blood:
21	chr7:110858722..110860508-chr7:110869419..110871427,2	K562	blood:
22	chr7:111178493..111181177-chr7:111184776..111187564,2	K562	blood:
23	chr7:111160191..111162473-chr7:111166967..111168569,3	K562	blood:
24	chr7:110904002..110906677-chr7:110908987..110911839,2	K562	blood:
25	chr7:110975243..110978153-chr7:110979724..110981495,2	K562	blood:
26	chr7:111031028..111033164-chr7:111033658..111035591,2	K562	blood:
27	chr7:110876830..110878652-chr7:110880390..110881983,2	K562	blood:
28	chr7:110843078..110846205-chr7:110849161..110854141,4	K562	blood:
29	chr7:110843665..110845702-chr7:110845783..110848771,2	K562	blood:
30	chr7:110846458..110850024-chr7:110851219..110853852,3	MCF-7	breast:
31	chr7:111150770..111153588-chr7:111154725..111157322,3	K562	blood:
32	chr7:110978869..110982048-chr7:110982767..110985792,3	K562	blood:
33	chr7:110729473..110730895-chr7:111126285..111127252,5	MCF-7	breast:
34	chr7:110730162..110730849-chr7:111126372..111127229,2	MCF-7	breast:
35	chr7:111079252..111081356-chr7:111081507..111084110,2	K562	blood:
36	chr7:111099278..111101723-chr7:111102972..111106150,5	K562	blood:
37	chr7:110946449..110947994-chr7:110949688..110952187,2	K562	blood:
38	chr7:110843078..110844596-chr7:110851457..110854141,2	K562	blood:
39	chr7:111164432..111166766-chr7:111167043..111169484,2	MCF-7	breast:
40	chr7:111132543..111134860-chr7:111136175..111139021,3	K562	blood:
41	chr7:110858379..110861216-chr7:110867269..110869936,2	MCF-7	breast:
42	chr7:110991909..110993941-chr7:110997470..110999246,2	K562	blood:
43	chr7:110958175..110962470-chr7:110967524..110970471,4	K562	blood:
44	chr7:111123975..111126506-chr7:111135381..111138359,2	K562	blood:
45	chr7:110934094..110935861-chr7:110939196..110941083,3	K562	blood:
46	chr6:31619932..31621913-chr7:111169935..111172752,2	K562	blood:
47	chr7:110907955..110909675-chr7:110912861..110914751,2	K562	blood:
48	chr7:111134697..111137160-chr7:111200355..111203674,3	K562	blood:
49	chr7:111164149..111166792-chr7:111174165..111176807,3	K562	blood:
50	chr7:110959334..110960882-chr7:110965813..110967484,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-DOCK4-7	chr7:110902289-110902553	expReg_chr7_8342_-

No data

Variant related genes	Relation type
ENSG00000227948	TF binding region
ENSG00000243621	TF binding region
IMMP2L	TF binding region
ENSG00000227948	CpG island
ENSG00000243621	CpG island
IMMP2L	CpG island
ENSG00000243621	chromatin interactions
ENSG00000184903	chromatin interactions
ENSG00000136856	chromatin interactions
ENSG00000173409	chromatin interactions
ENSG00000227948	chromatin interactions
ENSG00000173114	chromatin interactions
ENSG00000188825	chromatin interactions
ENSG00000240053	chromatin interactions
ENSG00000204463	chromatin interactions
ENSG00000143643	chromatin interactions
ENSG00000204444	chromatin interactions

Extended variants
information (count: 12364 )
Associated
traits (count: 101 )

Variant overlapped rSNPs/rCNVs (count:12364 , 50 per page) page: 1 2 3 4 5 6 7 ... 248

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs191946417	chr7:110839856-110839857	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs542566383	chr7:110839864-110839865	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs77082357	chr7:110839867-110839868	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs566963388	chr7:110839886-110839887	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs544787865	chr7:110839896-110839897	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs564476007	chr7:110839921-110839922	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs116101749	chr7:110839922-110839923	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs532252029	chr7:110839962-110839963	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs560143731	chr7:110840025-110840026	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs529236035	chr7:110840040-110840041	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs548909274	chr7:110840154-110840155	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs568810846	chr7:110840158-110840159	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs214454	chr7:110840236-110840237	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
14	rs184780695	chr7:110840306-110840307	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs189149673	chr7:110840307-110840308	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs115415939	chr7:110840341-110840342	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs533907101	chr7:110840371-110840372	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs372165309	chr7:110840435-110840436	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs553561874	chr7:110840544-110840545	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs375337896	chr7:110840584-110840585	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs567302607	chr7:110840601-110840602	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs180898794	chr7:110840628-110840629	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs536244178	chr7:110840636-110840637	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs80172100	chr7:110840637-110840638	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs547244356	chr7:110840651-110840652	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs35319082	chr7:110840660-110840661	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs200108865	chr7:110840664-110840665	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs71988348	chr7:110840665-110840666	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs58274613	chr7:110840671-110840672	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs374681042	chr7:110840672-110840673	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs544537546	chr7:110840673-110840674	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs368560155	chr7:110840674-110840675	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs558352383	chr7:110840682-110840683	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs113781103	chr7:110840794-110840795	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs578094568	chr7:110840804-110840805	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs145585495	chr7:110840811-110840812	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs113508148	chr7:110840825-110840826	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs371103247	chr7:110840827-110840828	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs148427985	chr7:110840847-110840848	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs529297307	chr7:110840856-110840857	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs574604902	chr7:110840863-110840864	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs542617233	chr7:110840875-110840876	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs145158311	chr7:110840906-110840907	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs531647278	chr7:110840956-110840957	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs184651159	chr7:110840971-110840972	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs571445604	chr7:110841002-110841003	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs527477601	chr7:110841083-110841084	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs147557643	chr7:110841100-110841101	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs534076057	chr7:110841265-110841266	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs60182421	chr7:110841275-110841276	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:101)

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
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
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
Acute myeloid leukemia	21251322	CNVD
Breast cancer	21785460	CNVD
Chronic myeloid leukemia	21384125	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Breast cancer	21364760	CNVD
lymphocytic leukemia	21291569	CNVD
Basal cell lymphoma	17053054	CNVD
Prostate cancer	16573809	CNVD
Medulloblastoma	16783165	CNVD
Melanoma	17363583	CNVD
Myelofibrosis	22110671	CNVD
Squamous cell cancer	20885788	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Breast cancer	16397240	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
Autism	19401682	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	19546859	CNVD
Schizophrenia	19546859	CNVD
Tourette syndrome	19546859	CNVD
Melanoma	19188590	CNVD
small cell lung cancer	20016488	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Dyslexia	22102821	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Attention deficit hyperactivity disorder	19546859	CNVD
Schizophrenia	23813976	CNVD
Autism	20531469	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Breast cancer	21509527	CNVD
Glioma	20126413	CNVD
early-passage human iPS cells	21368824	CNVD
Pancreatic cancer	17952125	CNVD
T-cell lymphomas	22341440	CNVD
Autism	20841430	CNVD
Autism	20685689	CNVD
Melanoma	20877625	CNVD

Chromatin state (count:1908 , 50 per page) page: 1 2 3 4 5 6 7 ... 39

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:110837400-110840000	Enhancers	Muscle Satellite Cultured Cells	--
2	chr7:110837600-110840000	Enhancers	Osteobl	bone
3	chr7:110838200-110846600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr7:110838400-110840200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
5	chr7:110838800-110864000	Weak transcription	Skeletal Muscle Female	skeletal muscle
6	chr7:110839600-110840000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
7	chr7:110842400-110842600	ZNF genes & repeats	Breast Myoepithelial Primary Cells	Breast
8	chr7:110842600-110852000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
9	chr7:110844400-110853000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
10	chr7:110845800-110846000	Enhancers	Left Ventricle	heart
11	chr7:110846000-110864000	Weak transcription	Left Ventricle	heart
12	chr7:110848400-110853000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
13	chr7:110850000-110851800	Enhancers	Muscle Satellite Cultured Cells	--
14	chr7:110850400-110851800	Enhancers	Osteobl	bone
15	chr7:110850800-110851400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
16	chr7:110850800-110851600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
17	chr7:110850800-110851600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
18	chr7:110851000-110851800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
19	chr7:110851000-110851800	Enhancers	HUVEC	blood vessel
20	chr7:110851200-110851600	Enhancers	ES-I3 Cell Line	embryonic stem cell
21	chr7:110851200-110851600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
22	chr7:110851200-110851600	Enhancers	HUES64 Cell Line	embryonic stem cell
23	chr7:110851200-110851600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
24	chr7:110851200-110851600	Enhancers	NH-A	brain
25	chr7:110851600-110854800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
26	chr7:110852000-110852400	ZNF genes & repeats	Breast Myoepithelial Primary Cells	Breast
27	chr7:110852000-110853000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
28	chr7:110852000-110853400	Weak transcription	Pancreas	Pancrea
29	chr7:110852400-110853000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
30	chr7:110852400-110853200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
31	chr7:110852400-110853400	Weak transcription	Fetal Intestine Small	intestine
32	chr7:110852800-110853800	Weak transcription	Cortex derived primary cultured neurospheres	brain
33	chr7:110853000-110853200	Enhancers	Spleen	Spleen
34	chr7:110853000-110853400	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
35	chr7:110853000-110853600	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
36	chr7:110853000-110853600	ZNF genes & repeats	Fetal Stomach	stomach
37	chr7:110853000-110853800	Genic enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
38	chr7:110853000-110853800	Enhancers	Placenta	Placenta
39	chr7:110853000-110854000	Strong transcription	Foreskin Melanocyte Primary Cells skin01	Skin
40	chr7:110853200-110853600	ZNF genes & repeats	Lung	lung
41	chr7:110853200-110853800	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
42	chr7:110853200-110853800	Strong transcription	Breast Myoepithelial Primary Cells	Breast
43	chr7:110853200-110853800	ZNF genes & repeats	Spleen	Spleen
44	chr7:110853400-110853600	Genic enhancers	Pancreas	Pancrea
45	chr7:110853400-110853800	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
46	chr7:110853400-110853800	ZNF genes & repeats	Fetal Intestine Small	intestine
47	chr7:110853600-110854400	Weak transcription	Pancreas	Pancrea
48	chr7:110853600-110855000	Weak transcription	Fetal Stomach	stomach
49	chr7:110853600-110857000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
50	chr7:110853800-110854200	Weak transcription	Spleen	Spleen

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