Variant report

Variant	nsv590206
Chromosome Location	chr3:46873957-46935527
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1703)
CpG islands
(count:3358)
Chromatin interactive
region (count:85)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1703 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr3:46877277-46877491	HepG2	liver:	n/a	n/a
2	ATF1	chr3:46935250-46935556	K562	blood:	n/a	n/a
3	ATF2	chr3:46886936-46887233	H1-hESC	embryonic stem cell:	n/a	n/a
4	ATF2	chr3:46935193-46935460	GM12878	blood:	n/a	n/a
5	ATF2	chr3:46935197-46935498	GM12878	blood:	n/a	n/a
6	ATF3	chr3:46876622-46876818	K562	blood:	n/a	n/a
7	ATF3	chr3:46876621-46876818	K562	blood:	n/a	n/a
8	ATF3	chr3:46935295-46935534	K562	blood:	n/a	n/a
9	BACH1	chr3:46886905-46888178	H1-hESC	embryonic stem cell:	n/a	n/a
10	BACH1	chr3:46933604-46934151	H1-hESC	embryonic stem cell:	n/a	n/a
11	BATF	chr3:46908306-46908463	GM12878	blood:	n/a	n/a
12	BHLHE40	chr3:46908281-46908558	GM12878	blood:	n/a	n/a
13	BHLHE40	chr3:46920347-46920695	GM12878	blood:	n/a	chr3:46920629-46920645
14	BHLHE40	chr3:46933586-46934024	GM12878	blood:	n/a	chr3:46933653-46933666
15	BHLHE40	chr3:46887011-46887611	GM12878	blood:	n/a	n/a
16	BHLHE40	chr3:46916049-46916314	GM12878	blood:	n/a	n/a
17	BHLHE40	chr3:46910968-46911286	K562	blood:	n/a	n/a
18	BHLHE40	chr3:46935299-46935304	GM12878	blood:	n/a	n/a
19	BHLHE40	chr3:46931712-46931927	K562	blood:	n/a	chr3:46931753-46931769
20	BHLHE40	chr3:46876585-46876919	K562	blood:	n/a	n/a
21	BHLHE40	chr3:46890068-46890315	K562	blood:	n/a	n/a
22	BHLHE40	chr3:46933640-46933993	A549	lung:	n/a	chr3:46933653-46933666
23	BHLHE40	chr3:46887699-46887844	K562	blood:	n/a	n/a
24	BHLHE40	chr3:46910992-46911290	GM12878	blood:	n/a	n/a
25	BHLHE40	chr3:46933330-46934052	K562	blood:	n/a	chr3:46933653-46933666
26	BHLHE40	chr3:46908311-46908663	K562	blood:	n/a	n/a
27	BHLHE40	chr3:46933523-46934086	HepG2	liver:	n/a	chr3:46933653-46933666
28	BHLHE40	chr3:46886933-46886936	K562	blood:	n/a	n/a
29	BRCA1	chr3:46930823-46930843	GM12878	blood:	n/a	n/a
30	BRCA1	chr3:46908315-46908492	GM12878	blood:	n/a	n/a
31	CBX3	chr3:46881875-46882432	HCT-116	colon:	n/a	n/a
32	CBX3	chr3:46881952-46882386	HCT-116	colon:	n/a	n/a
33	CBX3	chr3:46935173-46935468	K562	blood:	n/a	n/a
34	CBX3	chr3:46887146-46888067	K562	blood:	n/a	n/a
35	CBX3	chr3:46879790-46880135	K562	blood:	n/a	n/a
36	CBX3	chr3:46881973-46882315	K562	blood:	n/a	n/a
37	CBX3	chr3:46889974-46890395	K562	blood:	n/a	n/a
38	CBX3	chr3:46930945-46931127	K562	blood:	n/a	n/a
39	CBX3	chr3:46881972-46882321	K562	blood:	n/a	n/a
40	CBX3	chr3:46901723-46902115	K562	blood:	n/a	n/a
41	CCNT2	chr3:46923951-46924441	K562	blood:	n/a	chr3:46923962-46923971
42	CCNT2	chr3:46923207-46923400	K562	blood:	n/a	n/a
43	CCNT2	chr3:46887173-46887937	K562	blood:	n/a	n/a
44	CEBPB	chr3:46886710-46886785	K562	blood:	n/a	chr3:46886730-46886741
45	CEBPB	chr3:46923360-46923502	H1-hESC	embryonic stem cell:	n/a	n/a
46	CEBPB	chr3:46931913-46932113	K562	blood:	n/a	n/a
47	CEBPB	chr3:46916991-46917191	HepG2	liver:	n/a	n/a
48	CEBPB	chr3:46906680-46906931	IMR90	lung:	n/a	chr3:46906796-46906807
49	CEBPB	chr3:46886732-46886750	HepG2	liver:	n/a	n/a
50	CEBPB	chr3:46886581-46886869	H1-hESC	embryonic stem cell:	n/a	chr3:46886730-46886741

(count:3358 , 50 per page) page: 1 2 3 4 5 6 7 ... 68

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:46874907-46874957	HCM	heart:	n/a
2	chr3:46933864-46933914	HIPEpiC	eye:	n/a
3	chr3:46924768-46924818	NHBE	bronchial:	n/a
4	chr3:46874907-46874957	HCM	heart:	n/a
5	chr3:46933864-46933914	HIPEpiC	eye:	n/a
6	chr3:46924768-46924818	NHBE	bronchial:	n/a
7	chr3:46919454-46919504	AG04449	skin:	fetal
8	chr3:46922486-46922536	A549	lung:	n/a
9	chr3:46925081-46925131	HCT-116	colon:	n/a
10	chr3:46875872-46875922	HepG2	liver:	n/a
11	chr3:46927386-46927436	AG10803	skin:	n/a
12	chr3:46887449-46887499	HRPEpiC	eye:	n/a
13	chr3:46925524-46925574	HCF	heart:	n/a
14	chr3:46933808-46933858	HCF	heart:	n/a
15	chr3:46933782-46933832	PFSK-1	brain:	n/a
16	chr3:46875872-46875922	NB4	blood:	n/a
17	chr3:46918266-46918316	ovcar-3	ovarian:	n/a
18	chr3:46874907-46874957	NHDF-neo	bronchial:	n/a
19	chr3:46875768-46875818	NHDF-neo	bronchial:	n/a
20	chr3:46919066-46919116	SAEC	small airway:	n/a
21	chr3:46904643-46904693	AG10803	skin:	n/a
22	chr3:46887918-46887968	SK-N-SH	brain:	n/a
23	chr3:46874897-46874947	IMR90	lung:	fetal
24	chr3:46887918-46887968	SAEC	small airway:	n/a
25	chr3:46887195-46887245	H1-hESC	embryonic stem cell:	embryo
26	chr3:46924768-46924818	NHDF-neo	bronchial:	n/a
27	chr3:46918266-46918316	SKMC	muscle:	n/a
28	chr3:46906323-46906373	NT2-D1	testis:	n/a
29	chr3:46918356-46918406	HUVEC	blood vessel:	n/a
30	chr3:46924768-46924818	SK-N-SH	brain:	n/a
31	chr3:46875360-46875410	SK-N-SH_RA	brain:	n/a
32	chr3:46925181-46925231	HAEpiC	amniotic membrane:	n/a
33	chr3:46906323-46906373	GM19239	blood:	n/a
34	chr3:46875872-46875922	AG09319	gingival:	n/a
35	chr3:46919454-46919504	RPTEC	kidney:	n/a
36	chr3:46875436-46875486	HL-60	blood:	n/a
37	chr3:46924401-46924451	AG10803	skin:	n/a
38	chr3:46923546-46923596	K562	blood:	n/a
39	chr3:46875436-46875486	HEEpiC	esophagus:	n/a
40	chr3:46906385-46906435	AG04450	lung:	fetal
41	chr3:46875768-46875818	HUVEC	blood vessel:	n/a
42	chr3:46918266-46918316	HCPEpiC	choroid plexus:	n/a
43	chr3:46890144-46890194	HCF	heart:	n/a
44	chr3:46933864-46933914	A549	lung:	n/a
45	chr3:46925524-46925574	HEK293	kidney:	embryo
46	chr3:46923546-46923596	ECC-1	luminal epithelium:	n/a
47	chr3:46899455-46899505	T-47D	breast:	n/a
48	chr3:46887918-46887968	AG04450	lung:	fetal
49	chr3:46923068-46923118	GM06990	blood:	n/a
50	chr3:46906118-46906168	HL-60	blood:	n/a

(count:85 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr3:46888247..46890216-chr3:46894396..46896152,2	MCF-7	breast:
2	chr3:46901151..46902377-chr3:46936316..46937419,4	MCF-7	breast:
3	chr3:46905362..46907252-chr3:46950757..46952265,2	K562	blood:
4	chr3:46929163..46931629-chr3:46932279..46935009,2	K562	blood:
5	chr3:46707887..46708803-chr3:46920018..46920840,3	MCF-7	breast:
6	chr3:46907889..46909004-chr3:46936396..46937326,9	K562	blood:
7	chr3:46888493..46890387-chr3:46908192..46909889,2	K562	blood:
8	chr3:46882754..46884665-chr3:46886091..46888357,2	K562	blood:
9	chr3:46899974..46902852-chr3:46912143..46913911,3	K562	blood:
10	chr3:46901904..46902437-chr3:46950749..46951710,2	K562	blood:
11	chr3:46819637..46822469-chr3:46912934..46914923,2	K562	blood:
12	chr3:46906899..46908825-chr3:46935706..46937551,2	K562	blood:
13	chr17:41464813..41467414-chr3:46877462..46878983,3	K562	blood:
14	chr3:46905861..46908182-chr3:46909321..46912349,4	K562	blood:
15	chr3:46917376..46920621-chr3:46922888..46926605,5	K562	blood:
16	chr3:46888374..46889993-chr3:46908092..46909889,2	K562	blood:
17	chr3:46658701..46661042-chr3:46905477..46908148,2	MCF-7	breast:
18	chr3:46908049..46912169-chr3:46912978..46916098,5	K562	blood:
19	chr3:46899691..46902444-chr3:46923833..46927826,3	K562	blood:
20	chr3:46909467..46911881-chr3:46954858..46956855,2	K562	blood:
21	chr3:46926904..46929286-chr3:46949430..46951210,2	K562	blood:
22	chr3:46908943..46910828-chr3:46926732..46928602,2	K562	blood:
23	chr3:46875780..46877893-chr3:46878771..46880887,2	MCF-7	breast:
24	chr3:46908049..46912169-chr3:46912978..46916098,5	K562	blood:
25	chr3:46907987..46908617-chr3:47365202..47365982,2	K562	blood:
26	chr3:46893593..46896051-chr3:46906062..46908471,2	K562	blood:
27	chr3:46923291..46931131-chr3:46931662..46935716,9	K562	blood:
28	chr3:46892495..46894250-chr3:46920570..46922341,2	K562	blood:
29	chr3:46901375..46902381-chr3:46935997..46937249,3	K562	blood:
30	chr3:46927679..46930570-chr3:46933189..46935656,3	MCF-7	breast:
31	chr3:46888493..46890387-chr3:46908192..46909889,2	K562	blood:
32	chr3:46905861..46908182-chr3:46909321..46912349,4	K562	blood:
33	chr3:46923291..46931131-chr3:46931662..46935716,9	K562	blood:
34	chr3:46875780..46877893-chr3:46878771..46880887,2	MCF-7	breast:
35	chr3:46873969..46876010-chr3:46883057..46884646,2	K562	blood:
36	chr3:46915275..46917060-chr3:46923765..46925773,2	K562	blood:
37	chr3:46911199..46912719-chr3:46917160..46918725,2	MCF-7	breast:
38	chr3:46911199..46912719-chr3:46917160..46918725,2	MCF-7	breast:
39	chr3:46907898..46909023-chr3:46936371..46937303,3	MCF-7	breast:
40	chr3:46917885..46923537-chr3:46925586..46931315,6	MCF-7	breast:
41	chr3:46746642..46747266-chr3:46889901..46890658,2	MCF-7	breast:
42	chr3:46917885..46923537-chr3:46925586..46931315,6	MCF-7	breast:
43	chr3:46929163..46931629-chr3:46932279..46935009,2	K562	blood:
44	chr3:46798748..46799515-chr3:46907913..46908649,2	K562	blood:
45	chr17:41399072..41402668-chr3:46875963..46877484,6	K562	blood:
46	chr3:46907930..46908808-chr3:46950756..46951658,3	K562	blood:
47	chr3:46917376..46920621-chr3:46922888..46926605,5	K562	blood:
48	chr3:46893160..46895979-chr3:46900062..46901985,2	K562	blood:
49	chr3:46919067..46921668-chr3:46922191..46925334,3	K562	blood:
50	chr3:46899974..46902852-chr3:46912143..46913911,3	K562	blood:

(count:5 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PTH1R-1	chr3:46914185-46914431	NONHSAT089463
2	lnc-PRSS42-1	chr3:46876675-46877693	XLOC_003111
3	lnc-PRSS42-1	chr3:46885628-46885758	XLOC_003111
4	lnc-PRSS42-1	chr3:46888287-46888307	XLOC_003111
5	lnc-PTH1R-1	chr3:46916657-46917160	NONHSAT089463

No data

Variant related genes	Relation type
MYL3	TF binding region
PTH1R	TF binding region
PRSS42	TF binding region
ENSG00000268537	TF binding region
MYL3	CpG island
PTH1R	CpG island
PRSS42	CpG island
ENSG00000268537	CpG island
ENSG00000160801	chromatin interactions
ENSG00000178055	chromatin interactions
ENSG00000268537	chromatin interactions
ENSG00000160796	chromatin interactions
ENSG00000188825	chromatin interactions
ENSG00000160808	chromatin interactions
ENSG00000178038	chromatin interactions

Extended variants
information (count: 2122 )
Associated
traits (count: 109 )

Variant overlapped rSNPs/rCNVs (count:2122 , 50 per page) page: 1 2 3 4 5 6 7 ... 43

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7636089	chr3:46873957-46873958	Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs553229405	chr3:46873988-46873989	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs574513221	chr3:46873990-46873991	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs541785634	chr3:46874009-46874010	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs78573672	chr3:46874011-46874012	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs148877159	chr3:46874042-46874043	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs34130054	chr3:46874073-46874074	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs545978554	chr3:46874107-46874108	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs565127810	chr3:46874114-46874115	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs532333671	chr3:46874126-46874127	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs547744140	chr3:46874142-46874143	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs565953978	chr3:46874144-46874145	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs146487195	chr3:46874247-46874248	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs371004657	chr3:46874281-46874282	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs528661411	chr3:46874282-46874283	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs548119689	chr3:46874302-46874303	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs535420967	chr3:46874305-46874306	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs549146042	chr3:46874341-46874342	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs186113871	chr3:46874398-46874399	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs570738558	chr3:46874422-46874423	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs200786285	chr3:46874427-46874428	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs370252644	chr3:46874440-46874441	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs200671288	chr3:46874483-46874484	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs374513051	chr3:46874499-46874500	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs368789002	chr3:46874515-46874516	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs553266199	chr3:46874548-46874549	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs574752472	chr3:46874569-46874570	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs371034598	chr3:46874570-46874571	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs374184659	chr3:46874577-46874578	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs199822832	chr3:46874578-46874579	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs368580769	chr3:46874635-46874636	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs371639873	chr3:46874638-46874639	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs376248488	chr3:46874702-46874703	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs557373974	chr3:46874745-46874746	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs367672739	chr3:46874748-46874749	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs190192716	chr3:46874871-46874872	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs546316117	chr3:46874886-46874887	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs564405052	chr3:46874908-46874909	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs577135184	chr3:46874936-46874937	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs371844321	chr3:46874961-46874962	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs541194601	chr3:46874998-46874999	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs559686751	chr3:46875031-46875032	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs530062069	chr3:46875048-46875049	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs548176624	chr3:46875058-46875059	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs563327023	chr3:46875065-46875066	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs376588546	chr3:46875067-46875068	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs369788308	chr3:46875074-46875075	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs373961979	chr3:46875084-46875085	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs147909501	chr3:46875111-46875112	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs369861617	chr3:46875117-46875118	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:109)

Disease	PMID	Source
Lynch syndrome	18415027	CNVD
Renal cell carcinoma	18592004	CNVD
Acute myeloid leukemia	20729466	CNVD
Urothelial carcinoma	18382360	CNVD
Melanoma	18172304	CNVD
Cervical cancer	21062161	CNVD
Hirschsprung''s Disease	21712996	CNVD
Glioblastoma multiforme	21080181	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Insulin resistance	16721378	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	21484798	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Oral cancer	19627613	CNVD
Renal cell carcinoma	19461508	CNVD
Epithelial cancer	22065749	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Acute myeloid leukemia	16864856	CNVD
Liposarcoma	21253554	CNVD
Basal cell lymphoma	21115979	CNVD
Endometrial cancer	22040021	CNVD
Pancreatic endocrine tumor	20981439	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	17387387	CNVD
Oral cancer	21386901	CNVD
Cutaneous squamous cell carcinomas	19131950	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Retinoblastoma	21504564	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Renal cell carcinoma	21668985	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Thoracic aortic aneurysm	21092924	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	17603634	CNVD
Esophageal cancer	20955586	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Breast cancer	17133270	CNVD
Uveal melanoma	20484589	CNVD
Autism	22495311	CNVD
Melanoma	20688739	CNVD
Acute myeloid leukemia	21251322	CNVD
Hepatocellular carcinoma	16750200	CNVD
Cancer	21183584	CNVD
Kartagener syndrome	16639409	CNVD
Biliary cancer	19435499	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Bipolar disorder	20877625	CNVD
Bipolar disorder	21956041	CNVD
Bipolar disorder	22241247	CNVD
Biliary cancer	18923514	CNVD
Breast cancer	21509527	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	16397240	CNVD
Breast cancer	22032731	CNVD
Non-small cell lung cancer	20864512	CNVD
Colorectal cancer	16912164	CNVD
Non-small cell lung cancer	19010865	CNVD
Colorectal cancer	16272173	CNVD
Non-muscle invasive bladder neoplasm	19445696	CNVD
Acute myeloid leukemia	17268525	CNVD
Salivary gland tumor	18059337	CNVD
Gastric cancer	16891809	CNVD
Night blindness	17160897	CNVD
Cancer	17160897	CNVD
Breast cancer	20409316	CNVD
Lung cancer	17297452	CNVD
Multiple myeloma	16616336	CNVD
Effusion lymphoma	18079361	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Neuroblastoma	20406844	CNVD
Breast cancer	21785460	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	21045282	CNVD
Urothelial cell carcinoma	18451213	CNVD
Neuroblastoma	17327916	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Melanoma	17363583	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Adrenocortical carcinoma	18281524	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD

Chromatin state (count:2279 , 50 per page) page: 1 2 3 4 5 6 7 ... 46

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:46854200-46874800	Weak transcription	Psoas Muscle	Psoas
2	chr3:46867800-46877200	Weak transcription	Fetal Muscle Leg	muscle
3	chr3:46869400-46875600	Strong transcription	Skeletal Muscle Male	skeletal muscle
4	chr3:46870400-46876000	Strong transcription	Right Ventricle	heart
5	chr3:46870400-46886600	Weak transcription	Placenta Amnion	Placenta Amnion
6	chr3:46870600-46878800	Strong transcription	Left Ventricle	heart
7	chr3:46871400-46879400	Weak transcription	Fetal Heart	heart
8	chr3:46871800-46880200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
9	chr3:46872000-46874000	Weak transcription	GM12878-XiMat	blood
10	chr3:46872600-46874200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
11	chr3:46872800-46876800	Strong transcription	Skeletal Muscle Female	skeletal muscle
12	chr3:46873400-46877200	Weak transcription	Fetal Stomach	stomach
13	chr3:46873800-46879000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
14	chr3:46874000-46874400	Enhancers	GM12878-XiMat	blood
15	chr3:46874200-46875800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
16	chr3:46874400-46877200	Weak transcription	Fetal Intestine Small	intestine
17	chr3:46875600-46877400	Genic enhancers	Skeletal Muscle Male	skeletal muscle
18	chr3:46875800-46878400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
19	chr3:46876000-46877400	Weak transcription	Right Ventricle	heart
20	chr3:46876200-46876800	Enhancers	Pancreas	Pancrea
21	chr3:46876400-46876600	Enhancers	Duodenum Mucosa	Duodenum
22	chr3:46876600-46877600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
23	chr3:46876800-46877600	Weak transcription	Skeletal Muscle Female	skeletal muscle
24	chr3:46877200-46877400	Enhancers	Duodenum Mucosa	Duodenum
25	chr3:46877200-46877400	Enhancers	Fetal Brain Male	brain
26	chr3:46877200-46877400	Enhancers	Fetal Stomach	stomach
27	chr3:46877200-46877400	Enhancers	A549	lung
28	chr3:46877200-46877400	Flanking Bivalent TSS/Enh	K562	blood
29	chr3:46877200-46877600	Enhancers	Fetal Intestine Small	intestine
30	chr3:46877200-46877600	Enhancers	Fetal Muscle Trunk	muscle
31	chr3:46877200-46877600	Enhancers	Fetal Muscle Leg	muscle
32	chr3:46877400-46877600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
33	chr3:46877400-46877600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
34	chr3:46877400-46877800	Strong transcription	Right Ventricle	heart
35	chr3:46877400-46879400	Weak transcription	Skeletal Muscle Male	skeletal muscle
36	chr3:46877600-46879000	Strong transcription	Skeletal Muscle Female	skeletal muscle
37	chr3:46877800-46886600	Weak transcription	Right Ventricle	heart
38	chr3:46878800-46879200	Weak transcription	Left Ventricle	heart
39	chr3:46879000-46881800	Weak transcription	Skeletal Muscle Female	skeletal muscle
40	chr3:46879200-46879400	ZNF genes & repeats	Left Ventricle	heart
41	chr3:46879400-46880600	ZNF genes & repeats	Fetal Heart	heart
42	chr3:46879400-46880800	Strong transcription	Skeletal Muscle Male	skeletal muscle
43	chr3:46879400-46886600	Weak transcription	Left Ventricle	heart
44	chr3:46880600-46880800	Genic enhancers	Fetal Heart	heart
45	chr3:46880800-46882000	Enhancers	Fetal Heart	heart
46	chr3:46880800-46882000	Weak transcription	Skeletal Muscle Male	skeletal muscle
47	chr3:46881800-46882400	ZNF genes & repeats	Skeletal Muscle Female	skeletal muscle
48	chr3:46882000-46882200	Flanking Active TSS	Fetal Heart	heart
49	chr3:46882000-46882600	Strong transcription	Skeletal Muscle Male	skeletal muscle
50	chr3:46882200-46882400	Active TSS	Fetal Heart	heart

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