Variant report

Variant	nsv1039595
Chromosome Location	chr15:76431374-76483342
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1839)
CpG islands
(count:1099)
Chromatin interactive
region (count:74)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1839 , 50 per page) page: 1 2 3 4 5 6 7 ... 37

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr15:76443358-76443550	HepG2	liver:	n/a	n/a
2	ARID3A	chr15:76478041-76478258	HepG2	liver:	n/a	n/a
3	ARID3A	chr15:76443498-76443553	K562	blood:	n/a	n/a
4	ARID3A	chr15:76483064-76483427	HepG2	liver:	n/a	n/a
5	ATF2	chr15:76473823-76474454	GM12878	blood:	n/a	n/a
6	ATF2	chr15:76443272-76443758	GM12878	blood:	n/a	n/a
7	ATF2	chr15:76483089-76483813	GM12878	blood:	n/a	n/a
8	ATF2	chr15:76473954-76474425	GM12878	blood:	n/a	n/a
9	ATF2	chr15:76443260-76443649	H1-hESC	embryonic stem cell:	n/a	n/a
10	ATF3	chr15:76461421-76461690	K562	blood:	n/a	n/a
11	ATF3	chr15:76461375-76461737	H1-hESC	embryonic stem cell:	n/a	n/a
12	ATF3	chr15:76461499-76461617	GM12878	blood:	n/a	n/a
13	ATF3	chr15:76461359-76461682	GM12878	blood:	n/a	n/a
14	BACH1	chr15:76483297-76483365	H1-hESC	embryonic stem cell:	n/a	n/a
15	BATF	chr15:76473923-76474319	GM12878	blood:	n/a	chr15:76474119-76474130
16	BATF	chr15:76443332-76443766	GM12878	blood:	n/a	chr15:76443610-76443620
17	BATF	chr15:76473865-76474455	GM12878	blood:	n/a	chr15:76474119-76474130
18	BATF	chr15:76443394-76443743	GM12878	blood:	n/a	chr15:76443610-76443620
19	BCL11A	chr15:76474032-76474320	GM12878	blood:	n/a	n/a
20	BCL11A	chr15:76443382-76443708	GM12878	blood:	n/a	n/a
21	BCL11A	chr15:76443407-76443717	GM12878	blood:	n/a	n/a
22	BCL11A	chr15:76473914-76474363	GM12878	blood:	n/a	n/a
23	BCL3	chr15:76482892-76483810	A549	lung:	n/a	n/a
24	BCLAF1	chr15:76443247-76443763	GM12878	blood:	n/a	n/a
25	BCLAF1	chr15:76473905-76474445	GM12878	blood:	n/a	n/a
26	BCLAF1	chr15:76473788-76474517	GM12878	blood:	n/a	n/a
27	BHLHE40	chr15:76483088-76483437	GM12878	blood:	n/a	n/a
28	BHLHE40	chr15:76482536-76482865	K562	blood:	n/a	n/a
29	BHLHE40	chr15:76443352-76443674	GM12878	blood:	n/a	n/a
30	BHLHE40	chr15:76472876-76472910	HepG2	liver:	n/a	n/a
31	BHLHE40	chr15:76443337-76443588	K562	blood:	n/a	n/a
32	BHLHE40	chr15:76469949-76470149	A549	lung:	n/a	n/a
33	BHLHE40	chr15:76483122-76483431	K562	blood:	n/a	n/a
34	BHLHE40	chr15:76472787-76472910	K562	blood:	n/a	n/a
35	BHLHE40	chr15:76455772-76455880	K562	blood:	n/a	n/a
36	BHLHE40	chr15:76440299-76440592	GM12878	blood:	n/a	n/a
37	BHLHE40	chr15:76473924-76474330	GM12878	blood:	n/a	n/a
38	BRCA1	chr15:76483097-76483525	Hela-S3	cervix:	n/a	chr15:76483441-76483448
39	BRCA1	chr15:76483134-76483378	H1-hESC	embryonic stem cell:	n/a	n/a
40	BRCA1	chr15:76483167-76483490	HepG2	liver:	n/a	chr15:76483441-76483448
41	BRCA1	chr15:76455813-76456207	Hela-S3	cervix:	n/a	n/a
42	BRCA1	chr15:76440353-76440459	HepG2	liver:	n/a	n/a
43	CBX3	chr15:76477995-76478351	K562	blood:	n/a	n/a
44	CEBPB	chr15:76482808-76483429	H1-hESC	embryonic stem cell:	n/a	n/a
45	CEBPB	chr15:76455736-76456063	K562	blood:	n/a	chr15:76455897-76455908 chr15:76455897-76455908
46	CEBPB	chr15:76441608-76442115	IMR90	lung:	n/a	n/a
47	CEBPB	chr15:76455721-76456129	ECC-1	luminal epithelium:	n/a	chr15:76455897-76455908 chr15:76455897-76455908
48	CEBPB	chr15:76455786-76456001	K562	blood:	n/a	chr15:76455897-76455908 chr15:76455897-76455908
49	CEBPB	chr15:76443302-76443706	Hela-S3	cervix:	n/a	n/a
50	CEBPB	chr15:76455684-76456090	IMR90	lung:	n/a	chr15:76455897-76455908 chr15:76455897-76455908

(count:1099 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:76440405-76440455	H1-hESC	embryonic stem cell:	embryo
2	chr15:76440405-76440455	H1-hESC	embryonic stem cell:	embryo
3	chr15:76461960-76462010	HL-60	blood:	n/a
4	chr15:76440405-76440455	NB4	blood:	n/a
5	chr15:76444525-76444575	GM12892	blood:	n/a
6	chr15:76461960-76462010	HCPEpiC	choroid plexus:	n/a
7	chr15:76483201-76483251	HCM	heart:	n/a
8	chr15:76483281-76483331	HCF	heart:	n/a
9	chr15:76483281-76483331	U87	brain:	n/a
10	chr15:76440443-76440493	T-47D	breast:	n/a
11	chr15:76458365-76458415	AG09309	skin:	n/a
12	chr15:76483201-76483251	ovcar-3	ovarian:	n/a
13	chr15:76442477-76442527	SKMC	muscle:	n/a
14	chr15:76440448-76440498	IMR90	lung:	fetal
15	chr15:76483201-76483251	GM12878	blood:	n/a
16	chr15:76478102-76478152	HCF	heart:	n/a
17	chr15:76458372-76458422	GM06990	blood:	n/a
18	chr15:76470979-76471029	GM06990	blood:	n/a
19	chr15:76442477-76442527	AoSMC	blood vessel:	n/a
20	chr15:76458279-76458329	HRPEpiC	eye:	n/a
21	chr15:76458365-76458415	RPTEC	kidney:	n/a
22	chr15:76444525-76444575	GM12891	blood:	n/a
23	chr15:76440405-76440455	HMEC	breast:	n/a
24	chr15:76483201-76483251	AG04450	lung:	fetal
25	chr15:76461960-76462010	AoSMC	blood vessel:	n/a
26	chr15:76444525-76444575	SAEC	small airway:	n/a
27	chr15:76458279-76458329	AoSMC	blood vessel:	n/a
28	chr15:76470979-76471029	NB4	blood:	n/a
29	chr15:76483201-76483251	H1-hESC	embryonic stem cell:	embryo
30	chr15:76455848-76455898	PFSK-1	brain:	n/a
31	chr15:76475969-76476019	ovcar-3	ovarian:	n/a
32	chr15:76483201-76483251	CMK	blood:	n/a
33	chr15:76462821-76462871	HCM	heart:	n/a
34	chr15:76470979-76471029	HRCEpiC	kidney:	n/a
35	chr15:76455848-76455898	NH-A	brain:	n/a
36	chr15:76440448-76440498	HMEC	breast:	n/a
37	chr15:76440405-76440455	GM12892	blood:	n/a
38	chr15:76431858-76431908	NHBE	bronchial:	n/a
39	chr15:76462821-76462871	HPAEpiC	pulmonary alveolar:	n/a
40	chr15:76440448-76440498	HUVEC	blood vessel:	n/a
41	chr15:76458365-76458415	HAEpiC	amniotic membrane:	n/a
42	chr15:76478102-76478152	GM12878	blood:	n/a
43	chr15:76458365-76458415	BJ	skin:	n/a
44	chr15:76455848-76455898	AoSMC	blood vessel:	n/a
45	chr15:76458365-76458415	ProgFib	skin:	n/a
46	chr15:76458372-76458422	Hela-S3	cervix:	n/a
47	chr15:76440405-76440455	HRCEpiC	kidney:	n/a
48	chr15:76440448-76440498	HIPEpiC	eye:	n/a
49	chr15:76458372-76458422	AG10803	skin:	n/a
50	chr15:76458365-76458415	HCT-116	colon:	n/a

(count:74 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr15:76460346..76463407-chr15:76465556..76467922,3	MCF-7	breast:
2	chr15:76435308..76438673-chr15:76443082..76445810,3	K562	blood:
3	chr15:76482846..76483696-chr15:76577399..76578194,4	MCF-7	breast:
4	chr15:76348835..76350888-chr15:76431511..76432728,13	MCF-7	breast:
5	chr15:76350898..76351807-chr15:76431306..76432503,7	MCF-7	breast:
6	chr15:76453448..76455028-chr15:76460465..76463377,2	K562	blood:
7	chr15:76436435..76439411-chr15:76454805..76456724,2	K562	blood:
8	chr15:76482924..76483751-chr15:76625816..76626899,5	MCF-7	breast:
9	chr15:76478149..76479732-chr15:76481760..76484387,3	K562	blood:
10	chr15:76478027..76479862-chr15:76483019..76485634,3	MCF-7	breast:
11	chr15:76467419..76469629-chr15:76476906..76478729,2	MCF-7	breast:
12	chr15:76220909..76222483-chr15:76431367..76432547,6	MCF-7	breast:
13	chr15:76431446..76432246-chr15:76440422..76441109,2	MCF-7	breast:
14	chr15:76440174..76440912-chr15:76625983..76626603,2	MCF-7	breast:
15	chr15:76472338..76474227-chr15:76482406..76484297,2	K562	blood:
16	chr15:76441645..76443484-chr15:76650484..76652153,2	K562	blood:
17	chr15:76405575..76406307-chr15:76431978..76432508,2	MCF-7	breast:
18	chr15:76481529..76484202-chr15:76633877..76636476,2	K562	blood:
19	chr15:76349376..76350531-chr15:76431524..76433402,8	MCF-7	breast:
20	chr15:76460184..76462752-chr15:76465404..76467904,2	K562	blood:
21	chr15:76435308..76438673-chr15:76443082..76445810,3	K562	blood:
22	chr15:76482740..76483457-chr15:76626133..76626814,2	MCF-7	breast:
23	chr15:76482829..76483665-chr15:77158796..77159907,4	MCF-7	breast:
24	chr15:76457780..76460448-chr15:76461142..76462656,2	K562	blood:
25	chr15:76483246..76483790-chr15:77158830..77159724,2	K562	blood:
26	chr15:76440836..76444169-chr15:76451014..76453553,3	MCF-7	breast:
27	chr15:76221299..76222193-chr15:76443491..76444002,2	MCF-7	breast:
28	chr15:76460184..76462752-chr15:76465404..76467904,2	K562	blood:
29	chr15:76446927..76448705-chr15:76450684..76453682,2	MCF-7	breast:
30	chr15:76467419..76469629-chr15:76476906..76478729,2	MCF-7	breast:
31	chr15:76476723..76478991-chr15:76480313..76482582,2	K562	blood:
32	chr15:76452254..76455049-chr15:76455599..76457140,2	K562	blood:
33	chr15:76436946..76439521-chr3:195163273..195165269,2	MCF-7	breast:
34	chr15:76472338..76474227-chr15:76482406..76484297,2	K562	blood:
35	chr15:76350662..76351851-chr15:76431467..76432496,4	MCF-7	breast:
36	chr15:76482702..76486394-chr15:76633656..76636389,3	K562	blood:
37	chr15:76457780..76460448-chr15:76461142..76462656,2	K562	blood:
38	chr15:76455415..76457030-chr15:76460537..76462743,2	K562	blood:
39	chr15:76431477..76432448-chr15:76439936..76440516,2	K562	blood:
40	chr15:76452254..76455049-chr15:76455599..76457140,2	K562	blood:
41	chr15:76102008..76102960-chr15:76431567..76432789,7	MCF-7	breast:
42	chr15:76483216..76483808-chr15:76625887..76626857,3	K562	blood:
43	chr15:76435308..76437788-chr15:76443138..76445810,3	K562	blood:
44	chr15:76453448..76455028-chr15:76460465..76463377,2	K562	blood:
45	chr15:76102073..76103015-chr15:76443067..76443572,2	MCF-7	breast:
46	chr15:76455415..76457030-chr15:76460537..76462743,2	K562	blood:
47	chr15:76442105..76446396-chr15:76447199..76450761,5	MCF-7	breast:
48	chr15:76452837..76455028-chr15:76460465..76463193,2	K562	blood:
49	chr15:76483023..76483731-chr15:76527305..76528242,4	MCF-7	breast:
50	chr15:76477747..76478594-chr15:76625784..76626375,2	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000259422	TF binding region
C15orf27	TF binding region
ENSG00000259422	CpG island
C15orf27	CpG island
ENSG00000159556	chromatin interactions
ENSG00000114331	chromatin interactions
ENSG00000167196	chromatin interactions
ENSG00000169758	chromatin interactions
ENSG00000259422	chromatin interactions
ENSG00000270036	chromatin interactions
ENSG00000169752	chromatin interactions
ENSG00000259514	chromatin interactions

Extended variants
information (count: 2056 )
Associated
traits (count: 55 )

Variant overlapped rSNPs/rCNVs (count:2056 , 50 per page) page: 1 2 3 4 5 6 7 ... 42

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs536588000	chr15:76431393-76431394	Enhancers Weak transcription Strong transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs554886722	chr15:76431460-76431461	Enhancers Weak transcription Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs559407501	chr15:76431472-76431473	Enhancers Weak transcription Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs576379246	chr15:76431523-76431524	Enhancers Weak transcription Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs34672237	chr15:76431565-76431566	Enhancers Weak transcription Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs544634728	chr15:76431602-76431603	Enhancers Weak transcription Bivalent Enhancer Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs77345971	chr15:76431705-76431706	Enhancers Weak transcription Bivalent Enhancer Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs578039120	chr15:76431774-76431775	Enhancers Weak transcription Bivalent Enhancer Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs545483339	chr15:76431785-76431786	Enhancers Weak transcription Bivalent Enhancer Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs535165080	chr15:76431786-76431787	Enhancers Weak transcription Bivalent Enhancer Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs560565046	chr15:76431799-76431800	Enhancers Weak transcription Bivalent Enhancer Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs115598648	chr15:76431857-76431858	Enhancers Bivalent Enhancer Weak transcription Active TSS Bivalent/Poised TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs188677742	chr15:76431873-76431874	Enhancers Bivalent Enhancer Weak transcription Active TSS Bivalent/Poised TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs561266457	chr15:76431879-76431880	Enhancers Bivalent Enhancer Weak transcription Active TSS Bivalent/Poised TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs531848699	chr15:76431885-76431886	Enhancers Bivalent Enhancer Weak transcription Active TSS Bivalent/Poised TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs191189213	chr15:76431908-76431909	Enhancers Bivalent Enhancer Weak transcription Active TSS Bivalent/Poised TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs183525405	chr15:76431910-76431911	Enhancers Bivalent Enhancer Weak transcription Active TSS Bivalent/Poised TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs571175513	chr15:76431911-76431912	Enhancers Bivalent Enhancer Weak transcription Active TSS Bivalent/Poised TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs554772689	chr15:76431924-76431925	Enhancers Bivalent Enhancer Weak transcription Active TSS Bivalent/Poised TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs547458867	chr15:76431935-76431936	Enhancers Bivalent Enhancer Weak transcription Active TSS Bivalent/Poised TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs527832947	chr15:76431943-76431944	Enhancers Bivalent Enhancer Weak transcription Active TSS Bivalent/Poised TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs536474298	chr15:76431949-76431950	Enhancers Bivalent Enhancer Weak transcription Active TSS Bivalent/Poised TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs16967901	chr15:76432032-76432033	Enhancers Flanking Active TSS Bivalent Enhancer Active TSS Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs188213835	chr15:76432063-76432064	Enhancers Flanking Active TSS Bivalent Enhancer Active TSS Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs537295210	chr15:76432072-76432073	Enhancers Flanking Active TSS Bivalent Enhancer Active TSS Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs3021425	chr15:76432089-76432090	Enhancers Flanking Active TSS Bivalent Enhancer Active TSS Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs529419827	chr15:76432090-76432091	Enhancers Flanking Active TSS Bivalent Enhancer Active TSS Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs556332026	chr15:76432171-76432172	Enhancers Flanking Active TSS Bivalent Enhancer Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs537756098	chr15:76432196-76432197	Enhancers Flanking Active TSS Bivalent Enhancer Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs74917523	chr15:76432211-76432212	Enhancers Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs545208717	chr15:76432218-76432219	Enhancers Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs138896097	chr15:76432229-76432230	Enhancers Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs572177406	chr15:76432341-76432342	Enhancers Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs77267240	chr15:76432367-76432368	Enhancers Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs561102580	chr15:76432433-76432434	Enhancers Active TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs531882661	chr15:76432500-76432501	Enhancers Active TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs141805922	chr15:76432503-76432504	Enhancers Active TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs564768280	chr15:76432506-76432507	Enhancers Active TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs557321796	chr15:76432570-76432571	Enhancers Active TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs374051795	chr15:76432573-76432574	Enhancers Active TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs182229310	chr15:76432617-76432618	Active TSS Enhancers Flanking Active TSS Bivalent Enhancer Weak transcription Bivalent/Poised TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs529774731	chr15:76432625-76432626	Active TSS Enhancers Flanking Active TSS Bivalent Enhancer Weak transcription Bivalent/Poised TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs61744092	chr15:76432629-76432630	Active TSS Enhancers Flanking Active TSS Bivalent Enhancer Weak transcription Bivalent/Poised TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs187193237	chr15:76432667-76432668	Active TSS Enhancers Flanking Active TSS Bivalent Enhancer Weak transcription Bivalent/Poised TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs537387318	chr15:76432671-76432672	Active TSS Enhancers Flanking Active TSS Bivalent Enhancer Weak transcription Bivalent/Poised TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs552433933	chr15:76432673-76432674	Active TSS Enhancers Flanking Active TSS Bivalent Enhancer Weak transcription Bivalent/Poised TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs372347394	chr15:76432688-76432689	Active TSS Enhancers Flanking Active TSS Bivalent Enhancer Weak transcription Bivalent/Poised TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs190232921	chr15:76432695-76432696	Active TSS Enhancers Flanking Active TSS Bivalent Enhancer Weak transcription Bivalent/Poised TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs181884065	chr15:76432728-76432729	Active TSS Enhancers Flanking Active TSS Bivalent Enhancer Weak transcription Bivalent/Poised TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs553844695	chr15:76432746-76432747	Active TSS Enhancers Flanking Active TSS Bivalent Enhancer Weak transcription Bivalent/Poised TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:55)

Disease	PMID	Source
Ewing''s sarcoma	21437220	CNVD
Schizophrenia	19415332	CNVD
Breast cancer	22522925	CNVD
Wilms tumour	21544195	CNVD
cataract	16735990	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Medulloblastoma	21979893	CNVD
spastic paraplegia with thinning of corpus callosum	19105190	CNVD
Schizophrenia	21324950	CNVD
Astrocytoma	17387387	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Disease	21824424	CNVD
Melanoma	18172304	CNVD
Gastric cancer	17167181	CNVD
Neuroblastoma	19435921	CNVD
Colorectal cancer	19359472	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Colorectal cancer	16272173	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Multiple myeloma	17550852	CNVD
Intellectual disability	22102821	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute myeloid leukemia	20729466	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Multiple myeloma	20724749	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Prostate cancer	18632612	CNVD
small cell lung cancer	20016488	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Cancer	16751803	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Breast cancer	17133270	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	17322880	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Lung cancer	18438408	CNVD
Multiple myeloma	16616336	CNVD
Myelofibrosis	22110671	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Papillary thyroid carcinoma	22161024	CNVD
Autism	21480499	CNVD
Breast cancer	17603634	CNVD
Acute myeloid leukemia	16864856	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Breast cancer	21364760	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Breast cancer	21611746	CNVD

Chromatin state (count:1315 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:76416600-76431600	Weak transcription	Pancreas	Pancrea
2	chr15:76426400-76432000	Weak transcription	Skeletal Muscle Male	skeletal muscle
3	chr15:76428200-76432000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
4	chr15:76429000-76432000	Weak transcription	Brain Hippocampus Middle	brain
5	chr15:76429400-76442800	Weak transcription	Brain Inferior Temporal Lobe	brain
6	chr15:76429600-76442800	Weak transcription	Brain Angular Gyrus	brain
7	chr15:76430600-76431400	Strong transcription	Skeletal Muscle Female	skeletal muscle
8	chr15:76430600-76431800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
9	chr15:76430600-76432400	Enhancers	HMEC	breast
10	chr15:76430600-76432800	Enhancers	Breast Myoepithelial Primary Cells	Breast
11	chr15:76430800-76431400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
12	chr15:76430800-76431400	Flanking Active TSS	NHEK	skin
13	chr15:76430800-76432000	Enhancers	Esophagus	oesophagus
14	chr15:76430800-76432400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
15	chr15:76431000-76432200	Enhancers	iPS-18 Cell Line	embryonic stem cell
16	chr15:76431000-76432600	Enhancers	ES-I3 Cell Line	embryonic stem cell
17	chr15:76431000-76433000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
18	chr15:76431200-76432000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
19	chr15:76431200-76432200	Enhancers	HUES64 Cell Line	embryonic stem cell
20	chr15:76431200-76432600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
21	chr15:76431200-76432600	Enhancers	Placenta	Placenta
22	chr15:76431200-76432800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
23	chr15:76431200-76432800	Enhancers	Primary neutrophils fromperipheralblood	blood
24	chr15:76431200-76432800	Enhancers	Primary hematopoietic stem cells short term culture	blood
25	chr15:76431200-76432800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
26	chr15:76431200-76432800	Enhancers	GM12878-XiMat	blood
27	chr15:76431400-76431600	Enhancers	iPS-20b Cell Line	embryonic stem cell
28	chr15:76431400-76431800	Weak transcription	Skeletal Muscle Female	skeletal muscle
29	chr15:76431400-76431800	Enhancers	NHEK	skin
30	chr15:76431400-76432000	Enhancers	iPS-15b Cell Line	embryonic stem cell
31	chr15:76431400-76432000	Active TSS	Hela-S3	cervix
32	chr15:76431400-76432200	Enhancers	HUES48 Cell Line	embryonic stem cell
33	chr15:76431600-76432000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
34	chr15:76431600-76432400	Enhancers	Pancreas	Pancrea
35	chr15:76431600-76432600	Enhancers	Fetal Thymus	thymus
36	chr15:76431600-76432800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
37	chr15:76431600-76433000	Enhancers	H1 Cell Line	embryonic stem cell
38	chr15:76431600-76433000	Bivalent Enhancer	Fetal Muscle Trunk	muscle
39	chr15:76431800-76432000	Bivalent Enhancer	H9 Derived Neuron Cultured Cells	ES cell derived
40	chr15:76431800-76432000	Enhancers	HUES6 Cell Line	embryonic stem cell
41	chr15:76431800-76432000	Enhancers	Adipose Nuclei	Adipose
42	chr15:76431800-76432000	Bivalent/Poised TSS	HepG2	liver
43	chr15:76431800-76432000	Flanking Active TSS	NHEK	skin
44	chr15:76431800-76432200	Enhancers	Primary T helper cells PMA-I stimulated	--
45	chr15:76431800-76432200	Bivalent Enhancer	Primary T helper 17 cells PMA-I stimulated	--
46	chr15:76431800-76432200	Bivalent Enhancer	Fetal Intestine Large	intestine
47	chr15:76431800-76432200	Enhancers	Rectal Mucosa Donor 29	rectum
48	chr15:76431800-76432400	Enhancers	Primary B cells from peripheral blood	blood
49	chr15:76431800-76432400	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
50	chr15:76431800-76432400	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin

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