Variant report

Variant	nsv1024414
Chromosome Location	chr6:3862744-3898734
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:692)
CpG islands
(count:489)
Chromatin interactive
region (count:31)
LncRNA
region (count:16)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:692 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:3887338-3887833	HepG2	liver:	n/a	n/a
2	ARID3A	chr6:3872700-3873183	HepG2	liver:	n/a	n/a
3	ARID3A	chr6:3870006-3870777	HepG2	liver:	n/a	n/a
4	ARID3A	chr6:3891596-3891635	HepG2	liver:	n/a	n/a
5	BACH1	chr6:3886084-3886094	H1-hESC	embryonic stem cell:	n/a	n/a
6	BHLHE40	chr6:3885938-3886219	HepG2	liver:	n/a	n/a
7	BHLHE40	chr6:3871777-3872059	HepG2	liver:	n/a	n/a
8	BHLHE40	chr6:3896148-3896245	K562	blood:	n/a	n/a
9	BHLHE40	chr6:3872647-3873023	HepG2	liver:	n/a	n/a
10	BRCA1	chr6:3887657-3888016	Hela-S3	cervix:	n/a	n/a
11	CEBPB	chr6:3870126-3870625	HepG2	liver:	n/a	chr6:3870433-3870444
12	CEBPB	chr6:3888736-3889421	A549	lung:	n/a	chr6:3889099-3889110 chr6:3889128-3889139 chr6:3889041-3889052
13	CEBPB	chr6:3869998-3870713	A549	lung:	n/a	chr6:3870433-3870444
14	CEBPB	chr6:3884753-3884988	K562	blood:	n/a	chr6:3884865-3884876
15	CEBPB	chr6:3883201-3883467	HepG2	liver:	n/a	n/a
16	CEBPB	chr6:3883250-3883361	Hela-S3	cervix:	n/a	n/a
17	CEBPB	chr6:3872818-3873063	HepG2	liver:	n/a	n/a
18	CEBPB	chr6:3884755-3884949	HepG2	liver:	n/a	chr6:3884865-3884876
19	CEBPB	chr6:3888942-3889320	A549	lung:	n/a	chr6:3889099-3889110 chr6:3889128-3889139 chr6:3889041-3889052
20	CEBPB	chr6:3871826-3872130	HepG2	liver:	n/a	n/a
21	CEBPB	chr6:3888967-3889277	IMR90	lung:	n/a	chr6:3889099-3889110 chr6:3889128-3889139 chr6:3889041-3889052
22	CEBPB	chr6:3884741-3884943	HepG2	liver:	n/a	chr6:3884865-3884876
23	CEBPB	chr6:3884636-3885007	HepG2	liver:	n/a	chr6:3884865-3884876
24	CEBPB	chr6:3870290-3870528	HepG2	liver:	n/a	chr6:3870433-3870444
25	CEBPB	chr6:3889014-3889237	K562	blood:	n/a	chr6:3889099-3889110 chr6:3889128-3889139 chr6:3889041-3889052
26	CEBPB	chr6:3870076-3870649	A549	lung:	n/a	chr6:3870433-3870444
27	CEBPB	chr6:3871870-3872022	HepG2	liver:	n/a	n/a
28	CEBPB	chr6:3871794-3872106	HepG2	liver:	n/a	n/a
29	CEBPB	chr6:3888961-3889286	HepG2	liver:	n/a	chr6:3889099-3889110 chr6:3889128-3889139 chr6:3889041-3889052
30	CEBPB	chr6:3870209-3870626	A549	lung:	n/a	chr6:3870433-3870444
31	CEBPB	chr6:3883132-3883502	IMR90	lung:	n/a	n/a
32	CEBPB	chr6:3888932-3889288	Hela-S3	cervix:	n/a	chr6:3889099-3889110 chr6:3889128-3889139 chr6:3889041-3889052
33	CEBPB	chr6:3887441-3887742	HepG2	liver:	n/a	n/a
34	CEBPB	chr6:3884751-3884951	IMR90	lung:	n/a	chr6:3884865-3884876
35	CEBPB	chr6:3870040-3870543	HepG2	liver:	n/a	chr6:3870433-3870444
36	CEBPB	chr6:3870079-3870592	HepG2	liver:	n/a	chr6:3870433-3870444
37	CTCF	chr6:3885795-3886263	HepG2	liver:	n/a	chr6:3886038-3886051 chr6:3886038-3886046
38	CTCF	chr6:3887702-3887921	SK-N-SH_RA	brain:	n/a	n/a
39	CTCF	chr6:3885860-3886010	WI-38	lung:	n/a	n/a
40	CTCF	chr6:3887760-3887910	HVMF	connective:	n/a	n/a
41	CTCF	chr6:3885920-3886070	GM06990	blood:	n/a	chr6:3886038-3886051 chr6:3886038-3886046
42	CTCF	chr6:3885840-3885990	GM12865	blood:	n/a	n/a
43	CTCF	chr6:3885980-3886130	AG04449	skin:	n/a	chr6:3886038-3886051 chr6:3886038-3886046
44	CTCF	chr6:3885917-3886166	MCF-7	breast:	n/a	chr6:3886038-3886051 chr6:3886038-3886046
45	CTCF	chr6:3887760-3887910	HCPEpiC	choroid plexus:	n/a	n/a
46	CTCF	chr6:3887780-3887930	BE2_C	brain:	n/a	n/a
47	CTCF	chr6:3885920-3886070	AG10803	skin:	n/a	chr6:3886038-3886051 chr6:3886038-3886046
48	CTCF	chr6:3885940-3886090	GM12878	blood:	n/a	chr6:3886038-3886051 chr6:3886038-3886046
49	CTCF	chr6:3887780-3887930	AoAF	blood vessel:	n/a	n/a
50	CTCF	chr6:3885960-3886110	BE2_C	brain:	n/a	chr6:3886038-3886051 chr6:3886038-3886046

(count:489 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:3884445-3884495	HEEpiC	esophagus:	n/a
2	chr6:3884445-3884495	HEEpiC	esophagus:	n/a
3	chr6:3895506-3895556	HEK293	kidney:	embryo
4	chr6:3879941-3879991	HRCEpiC	kidney:	n/a
5	chr6:3884445-3884495	MCF10A-Er-Src	breast:	n/a
6	chr6:3884445-3884495	AG04449	skin:	fetal
7	chr6:3895506-3895556	HL-60	blood:	n/a
8	chr6:3869142-3869192	CMK	blood:	n/a
9	chr6:3880016-3880066	HL-60	blood:	n/a
10	chr6:3867369-3867419	SK-N-SH	brain:	n/a
11	chr6:3879941-3879991	HPAEpiC	pulmonary alveolar:	n/a
12	chr6:3879941-3879991	LNCaP	prostate:	n/a
13	chr6:3884445-3884495	HAEpiC	amniotic membrane:	n/a
14	chr6:3869142-3869192	Jurkat	blood:	n/a
15	chr6:3895506-3895556	HNPCEpiC	eye:	n/a
16	chr6:3879941-3879991	HL-60	blood:	n/a
17	chr6:3880154-3880204	Hela-S3	cervix:	n/a
18	chr6:3879941-3879991	NH-A	brain:	n/a
19	chr6:3880016-3880066	HRE	kidney:	n/a
20	chr6:3880154-3880204	MCF10A-Er-Src	breast:	n/a
21	chr6:3866461-3866511	SK-N-SH_RA	brain:	n/a
22	chr6:3869142-3869192	HCF	heart:	n/a
23	chr6:3869142-3869192	AG04450	lung:	fetal
24	chr6:3867369-3867419	ovcar-3	ovarian:	n/a
25	chr6:3884445-3884495	NHBE	bronchial:	n/a
26	chr6:3884445-3884495	GM12878	blood:	n/a
27	chr6:3895506-3895556	GM12892	blood:	n/a
28	chr6:3867369-3867419	ECC-1	luminal epithelium:	n/a
29	chr6:3866461-3866511	Jurkat	blood:	n/a
30	chr6:3866461-3866511	GM12892	blood:	n/a
31	chr6:3880016-3880066	GM12891	blood:	n/a
32	chr6:3895506-3895556	SKMC	muscle:	n/a
33	chr6:3879941-3879991	PrEC	prostate:	n/a
34	chr6:3880016-3880066	PANC-1	pancreas:	n/a
35	chr6:3867369-3867419	SAEC	small airway:	n/a
36	chr6:3880016-3880066	AG04449	skin:	fetal
37	chr6:3884445-3884495	HRCEpiC	kidney:	n/a
38	chr6:3869142-3869192	GM12891	blood:	n/a
39	chr6:3869142-3869192	GM12892	blood:	n/a
40	chr6:3895506-3895556	NHBE	bronchial:	n/a
41	chr6:3880016-3880066	HEK293	kidney:	embryo
42	chr6:3880154-3880204	HCT-116	colon:	n/a
43	chr6:3867369-3867419	Caco-2	colon:	n/a
44	chr6:3869142-3869192	SAEC	small airway:	n/a
45	chr6:3866461-3866511	AG09309	skin:	n/a
46	chr6:3879941-3879991	ProgFib	skin:	n/a
47	chr6:3880016-3880066	U87	brain:	n/a
48	chr6:3879941-3879991	GM12878	blood:	n/a
49	chr6:3869142-3869192	HRCEpiC	kidney:	n/a
50	chr6:3866461-3866511	HCF	heart:	n/a

(count:31 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:3897113..3898647-chr6:3908931..3910649,2	K562	blood:
2	chr6:3887694..3888205-chr6:3933337..3933919,2	MCF-7	breast:
3	chr6:3868137..3869646-chr6:4018398..4020880,2	K562	blood:
4	chr6:3871880..3874802-chr6:3880122..3882754,2	K562	blood:
5	chr6:3888924..3890734-chr6:3899675..3901360,2	K562	blood:
6	chr6:3886153..3887670-chr6:3930448..3932083,2	MCF-7	breast:
7	chr6:3885866..3888171-chr6:3928064..3930488,2	K562	blood:
8	chr6:3885565..3889777-chr6:3889921..3893040,4	K562	blood:
9	chr6:3742444..3743185-chr6:3885595..3886459,4	MCF-7	breast:
10	chr6:3748211..3749200-chr6:3870044..3870745,2	MCF-7	breast:
11	chr6:3849059..3849875-chr6:3887505..3888067,2	MCF-7	breast:
12	chr6:3894615..3896177-chr6:3901415..3904288,2	K562	blood:
13	chr6:3897113..3898789-chr6:3908137..3910649,3	K562	blood:
14	chr6:3835181..3835842-chr6:3885672..3886503,2	MCF-7	breast:
15	chr6:3884903..3886478-chr6:3933004..3934024,8	MCF-7	breast:
16	chr6:3752245..3754417-chr6:3884478..3887237,2	MCF-7	breast:
17	chr6:3885956..3886617-chr6:3978023..3978718,2	MCF-7	breast:
18	chr6:3867578..3871255-chr6:3875568..3878363,3	MCF-7	breast:
19	chr6:3885071..3886983-chr6:3976362..3978692,2	MCF-7	breast:
20	chr6:3897909..3902594-chr6:3909814..3914054,5	MCF-7	breast:
21	chr6:3851436..3854128-chr6:3866055..3868031,2	K562	blood:
22	chr6:3871880..3874802-chr6:3880122..3882754,2	K562	blood:
23	chr6:3885578..3886792-chr6:3932972..3933948,3	K562	blood:
24	chr14:31126982..31127513-chr6:3887375..3888256,2	MCF-7	breast:
25	chr6:3867578..3871255-chr6:3875568..3878363,3	MCF-7	breast:
26	chr6:3885637..3886297-chr6:3933085..3933964,3	MCF-7	breast:
27	chr6:3884416..3886270-chr6:3912454..3915389,2	MCF-7	breast:
28	chr6:3856672..3859374-chr6:3861006..3863463,3	K562	blood:
29	chr6:3885565..3889777-chr6:3889921..3893040,4	K562	blood:
30	chr6:3748208..3748986-chr6:3887304..3888731,4	MCF-7	breast:
31	chr6:3896820..3898525-chr6:3975512..3978304,2	K562	blood:

(count:16 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FAM50B-2	chr6:3894074-3894524	ENSG00000233068
2	lnc-FAM50B-2	chr6:3894272-3894524	NONHSAT107238
3	lnc-PXDC1-12	chr6:3865233-3865272	NONHSAT107222
4	lnc-PXDC1-13	chr6:3864672-3864953	NONHSAT107226
5	lnc-PXDC1-15	chr6:3887292-3887558	NONHSAT107235
6	lnc-PXDC1-15	chr6:3887315-3887572	NONHSAT107236
7	lnc-PXDC1-15	chr6:3887291-3887572	NONHSAT107234
8	lnc-C6orf146-3	chr6:3898392-3899699	NONHSAT107241
9	lnc-PXDC1-15	chr6:3887290-3887558	NONHSAT107231
10	lnc-PXDC1-15	chr6:3884439-3884551	NONHSAT107231
11	lnc-FAM50B-2	chr6:3893359-3893485	NONHSAT107238
12	lnc-FAM50B-2	chr6:3893713-3893776	NONHSAT107238
13	lnc-PXDC1-15	chr6:3897123-3897162	NONHSAT107231
14	lnc-FAM50B-2	chr6:3894273-3894524	XLOC_005137
15	lnc-FAM50B-2	chr6:3893714-3893776	XLOC_005137
16	lnc-FAM50B-2	chr6:3893360-3893485	XLOC_005137

No data

Variant related genes	Relation type
ENSG00000233068	TF binding region
ENSG00000233068	CpG island
ENSG00000219992	chromatin interactions
ENSG00000145945	chromatin interactions
ENSG00000216657	chromatin interactions
ENSG00000260604	chromatin interactions
ENSG00000272248	chromatin interactions
ENSG00000168994	chromatin interactions
ENSG00000218472	chromatin interactions

Extended variants
information (count: 1509 )
Associated
traits (count: 91 )

Variant overlapped rSNPs/rCNVs (count:1509 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs527366554	chr6:3862750-3862751	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs547217666	chr6:3862782-3862783	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs567051976	chr6:3862887-3862888	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs139887155	chr6:3862917-3862918	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs558738191	chr6:3862928-3862929	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs569177577	chr6:3862971-3862972	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs114721698	chr6:3862985-3862986	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs9392531	chr6:3863025-3863026	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs190382500	chr6:3863026-3863027	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs369939163	chr6:3863030-3863031	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs540717000	chr6:3863053-3863054	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs181920753	chr6:3863118-3863119	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs564581088	chr6:3863123-3863124	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs138107251	chr6:3863135-3863136	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs201500036	chr6:3863139-3863140	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs150242928	chr6:3863140-3863141	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs138840905	chr6:3863147-3863148	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs10675981	chr6:3863150-3863151	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs77746454	chr6:3863151-3863152	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs543961557	chr6:3863172-3863173	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs530313883	chr6:3863181-3863182	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs545985273	chr6:3863182-3863183	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs373094208	chr6:3863183-3863184	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs547358323	chr6:3863184-3863185	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs115077611	chr6:3863227-3863228	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs531613506	chr6:3863259-3863260	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs369037349	chr6:3863316-3863317	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs371523792	chr6:3863320-3863321	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs541791389	chr6:3863322-3863323	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs560753754	chr6:3863332-3863333	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs367805854	chr6:3863391-3863392	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs11327062	chr6:3863392-3863393	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs398000216	chr6:3863409-3863410	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs201040197	chr6:3863419-3863420	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs547373268	chr6:3863429-3863430	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs11242887	chr6:3863470-3863471	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs549255069	chr6:3863473-3863474	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs532881578	chr6:3863498-3863499	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs566077902	chr6:3863523-3863524	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs552327211	chr6:3863540-3863541	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs569138922	chr6:3863568-3863569	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs538518946	chr6:3863575-3863576	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs200137323	chr6:3863587-3863588	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs555008317	chr6:3863624-3863625	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs534569455	chr6:3863636-3863637	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs568736852	chr6:3863638-3863639	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs533898348	chr6:3863721-3863722	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs554151920	chr6:3863874-3863875	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs577384374	chr6:3863877-3863878	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs546345973	chr6:3863911-3863912	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:91)

Disease	PMID	Source
Developmental delay	19490664	CNVD
Cancer	21183584	CNVD
Multiple Epiphyseal Dysplasia	20877625	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Glaucoma	18694899	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Prostate cancer	16573809	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	17603634	CNVD
Cancer	20164920	CNVD
Colorectal cancer	21297112	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Follicular lymphoma	20505157	CNVD
Glioblastoma multiforme	21080181	CNVD
Ewing''s sarcoma	21437220	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Leukemia	21518781	CNVD
Cancer	21637783	CNVD
Facial dysmorphism	22105932	CNVD
Medulloblastoma	21979893	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Endometrial cancer	22040021	CNVD
Acute myeloid leukemia	16864856	CNVD
Breast cancer	21264507	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	16751803	CNVD
Bladder cancer	19088036	CNVD
Wilms tumour	21544195	CNVD
Uveal melanoma	21693616	CNVD
Biliary cancer	19435499	CNVD
Malaria	21533027	CNVD
Retinoblastoma	19183342	CNVD
Acute myeloid leukemia	20729466	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Prostate cancer	18632612	CNVD
Myelodysplastic syndrome	21251322	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Breast cancer	21858162	CNVD
Lung cancer	18438408	CNVD
Bladder cancer	21909424	CNVD
Multiple myeloma	17550852	CNVD
Ewing''s sarcoma	17952124	CNVD
Breast cancer	21364760	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Gastric cancer	16891809	CNVD
Ovarian cancer	21781307	CNVD
Autism	22495311	CNVD
Autism	21448237	CNVD
Cancer	20164919	CNVD
Myelofibrosis	22110671	CNVD
Uveal melanoma	20484589	CNVD
Melanoma	18172304	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Breast cancer	22844521	CNVD
HIV/AIDS	22844521	CNVD
Ovarian cancer	22844521	CNVD
Prostate cancer	22844521	CNVD
Psoriasis	22844521	CNVD
Rheumatoid arthritis	22844521	CNVD
Sclerosis systemic	22844521	CNVD
Systemic lupus erythematosus	22844521	CNVD
Breast cancer	22522925	CNVD
Breast cancer	21552322	CNVD
Immune disease	21076436	CNVD
Autoimmune disease	19135723	CNVD
Systemic lupus erythematosus	17953491	CNVD
Recurrent Infections	22737222	CNVD
Systemic lupus erythematosus	21904924	CNVD
Ependymoma	19289631	CNVD
small cell lung cancer	20016488	CNVD
Gestational infection	22844521	CNVD
Head circumference	22844521	CNVD
Infertility	22844521	CNVD
Recurrent birth weight diabetes	22844521	CNVD
Obesity	22844521	CNVD
Recurrent pregnancy loss	22844521	CNVD
Intellectual disability	21811512	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:649 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:3855000-3869600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr6:3861400-3862800	Enhancers	HUES6 Cell Line	embryonic stem cell
3	chr6:3861400-3863000	Enhancers	iPS-18 Cell Line	embryonic stem cell
4	chr6:3861600-3862800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
5	chr6:3862000-3862800	Enhancers	iPS-20b Cell Line	embryonic stem cell
6	chr6:3862000-3863000	Enhancers	H1 Cell Line	embryonic stem cell
7	chr6:3862000-3865000	Weak transcription	HepG2	liver
8	chr6:3862200-3862800	Enhancers	HUES64 Cell Line	embryonic stem cell
9	chr6:3862200-3863000	Enhancers	HUES48 Cell Line	embryonic stem cell
10	chr6:3862200-3868600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
11	chr6:3862400-3867400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
12	chr6:3862600-3867400	Weak transcription	NHEK	skin
13	chr6:3862800-3867200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
14	chr6:3865000-3865200	Enhancers	HepG2	liver
15	chr6:3865800-3866000	Active TSS	Gastric	stomach
16	chr6:3866000-3869600	Weak transcription	Gastric	stomach
17	chr6:3867200-3867400	Enhancers	Fetal Muscle Trunk	muscle
18	chr6:3867200-3867600	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
19	chr6:3867200-3868200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
20	chr6:3867200-3868200	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
21	chr6:3867200-3868600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
22	chr6:3867200-3869600	Enhancers	Fetal Intestine Large	intestine
23	chr6:3867200-3869600	Enhancers	Fetal Intestine Small	intestine
24	chr6:3867200-3871400	Enhancers	Stomach Mucosa	stomach
25	chr6:3867400-3867600	Enhancers	Esophagus	oesophagus
26	chr6:3867400-3868800	Enhancers	NHEK	skin
27	chr6:3867400-3869200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
28	chr6:3867600-3867800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
29	chr6:3867600-3867800	Flanking Active TSS	Primary T helper 17 cells PMA-I stimulated	--
30	chr6:3867600-3868000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
31	chr6:3867600-3868000	Enhancers	Osteobl	bone
32	chr6:3867600-3868200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
33	chr6:3867600-3868200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
34	chr6:3867600-3868200	Enhancers	Muscle Satellite Cultured Cells	--
35	chr6:3867600-3868200	Enhancers	NHDF-Ad	bronchial
36	chr6:3867600-3869200	Enhancers	Small Intestine	intestine
37	chr6:3867600-3870200	Enhancers	Fetal Muscle Leg	muscle
38	chr6:3867600-3870600	Enhancers	Primary T regulatory cells fromperipheralblood	blood
39	chr6:3867600-3871200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
40	chr6:3867800-3868200	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
41	chr6:3867800-3868800	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
42	chr6:3867800-3868800	Enhancers	Primary T helper naive cells from peripheral blood	blood
43	chr6:3867800-3869200	Enhancers	HMEC	breast
44	chr6:3867800-3869400	Enhancers	Brain Hippocampus Middle	brain
45	chr6:3868000-3868200	Enhancers	Brain Germinal Matrix	brain
46	chr6:3868000-3868200	Enhancers	Rectal Mucosa Donor 31	rectum
47	chr6:3868000-3868600	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
48	chr6:3868000-3869000	Flanking Active TSS	Osteobl	bone
49	chr6:3868000-3869600	Enhancers	A549	lung
50	chr6:3868000-3869800	Enhancers	Cortex derived primary cultured neurospheres	brain

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