Variant report

Variant	nsv1041609
Chromosome Location	chr15:33148035-33355999
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2534)
CpG islands
(count:1712)
Chromatin interactive
region (count:86)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2534 , 50 per page) page: 1 2 3 4 5 6 7 ... 51

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr15:33159576-33159767	K562	blood:	n/a	n/a
2	ARID3A	chr15:33287094-33287423	K562	blood:	n/a	n/a
3	ATF1	chr15:33162681-33163010	K562	blood:	n/a	n/a
4	ATF1	chr15:33218767-33218893	K562	blood:	n/a	n/a
5	ATF1	chr15:33172177-33172299	K562	blood:	n/a	n/a
6	ATF2	chr15:33200491-33201087	GM12878	blood:	n/a	n/a
7	ATF2	chr15:33191348-33191883	H1-hESC	embryonic stem cell:	n/a	n/a
8	ATF2	chr15:33191373-33191925	H1-hESC	embryonic stem cell:	n/a	n/a
9	ATF3	chr15:33162589-33163012	K562	blood:	n/a	n/a
10	BACH1	chr15:33159494-33159789	H1-hESC	embryonic stem cell:	n/a	n/a
11	BACH1	chr15:33221160-33221387	H1-hESC	embryonic stem cell:	n/a	n/a
12	BACH1	chr15:33173812-33174063	H1-hESC	embryonic stem cell:	n/a	n/a
13	BACH1	chr15:33248180-33248533	H1-hESC	embryonic stem cell:	n/a	n/a
14	BACH1	chr15:33175154-33175210	H1-hESC	embryonic stem cell:	n/a	n/a
15	BACH1	chr15:33165863-33166308	H1-hESC	embryonic stem cell:	n/a	n/a
16	BACH1	chr15:33175656-33175900	H1-hESC	embryonic stem cell:	n/a	n/a
17	BACH1	chr15:33164881-33164895	K562	blood:	n/a	n/a
18	BACH1	chr15:33165875-33166293	K562	blood:	n/a	n/a
19	BATF	chr15:33216580-33216867	GM12878	blood:	n/a	n/a
20	BATF	chr15:33200675-33201039	GM12878	blood:	n/a	n/a
21	BATF	chr15:33162674-33163028	GM12878	blood:	n/a	chr15:33162820-33162831
22	BATF	chr15:33162661-33162960	GM12878	blood:	n/a	chr15:33162820-33162831
23	BATF	chr15:33216573-33216893	GM12878	blood:	n/a	n/a
24	BCL11A	chr15:33191354-33191789	H1-hESC	embryonic stem cell:	n/a	chr15:33191642-33191655
25	BCL11A	chr15:33162643-33162955	GM12878	blood:	n/a	n/a
26	BCL11A	chr15:33162608-33162974	GM12878	blood:	n/a	n/a
27	BCL11A	chr15:33200755-33201026	GM12878	blood:	n/a	chr15:33200826-33200835
28	BCL11A	chr15:33216557-33216912	GM12878	blood:	n/a	n/a
29	BCL11A	chr15:33200637-33201056	GM12878	blood:	n/a	chr15:33200826-33200835
30	BCL11A	chr15:33191394-33191852	H1-hESC	embryonic stem cell:	n/a	chr15:33191642-33191655
31	BCL3	chr15:33158768-33159753	A549	lung:	n/a	n/a
32	BCL3	chr15:33158650-33159539	A549	lung:	n/a	n/a
33	BCLAF1	chr15:33200479-33201139	GM12878	blood:	n/a	chr15:33200826-33200835
34	BCLAF1	chr15:33216507-33216804	GM12878	blood:	n/a	n/a
35	BHLHE40	chr15:33247941-33248082	K562	blood:	n/a	n/a
36	BHLHE40	chr15:33200447-33201288	GM12878	blood:	n/a	n/a
37	BHLHE40	chr15:33216326-33216884	GM12878	blood:	n/a	n/a
38	BHLHE40	chr15:33162181-33162900	K562	blood:	n/a	n/a
39	BHLHE40	chr15:33191303-33191733	GM12878	blood:	n/a	n/a
40	BHLHE40	chr15:33159651-33159697	K562	blood:	n/a	n/a
41	BHLHE40	chr15:33297971-33297975	GM12878	blood:	n/a	n/a
42	BRCA1	chr15:33314097-33314500	Hela-S3	cervix:	n/a	n/a
43	CBX3	chr15:33148028-33148433	HCT-116	colon:	n/a	n/a
44	CBX3	chr15:33340492-33340828	HCT-116	colon:	n/a	n/a
45	CBX3	chr15:33305905-33306560	HCT-116	colon:	n/a	n/a
46	CCNT2	chr15:33162693-33162976	K562	blood:	n/a	n/a
47	CEBPB	chr15:33164686-33165549	IMR90	lung:	n/a	n/a
48	CEBPB	chr15:33219343-33219706	A549	lung:	n/a	chr15:33219513-33219524
49	CEBPB	chr15:33245348-33245587	IMR90	lung:	n/a	n/a
50	CEBPB	chr15:33266880-33267254	IMR90	lung:	n/a	chr15:33267062-33267073 chr15:33267033-33267045

(count:1712 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:33259575-33259625	HUVEC	blood vessel:	n/a
2	chr15:33177867-33177917	ovcar-3	ovarian:	n/a
3	chr15:33259575-33259625	PFSK-1	brain:	n/a
4	chr15:33311980-33312030	U87	brain:	n/a
5	chr15:33259575-33259625	HUVEC	blood vessel:	n/a
6	chr15:33177867-33177917	ovcar-3	ovarian:	n/a
7	chr15:33259575-33259625	PFSK-1	brain:	n/a
8	chr15:33311980-33312030	U87	brain:	n/a
9	chr15:33245281-33245331	ProgFib	skin:	n/a
10	chr15:33310931-33310981	Caco-2	colon:	n/a
11	chr15:33311031-33311081	NHDF-neo	bronchial:	n/a
12	chr15:33310931-33310981	GM06990	blood:	n/a
13	chr15:33311738-33311788	T-47D	breast:	n/a
14	chr15:33235802-33235852	HPAEpiC	pulmonary alveolar:	n/a
15	chr15:33310931-33310981	Jurkat	blood:	n/a
16	chr15:33165563-33165613	AG10803	skin:	n/a
17	chr15:33191698-33191748	MCF-7	breast:	n/a
18	chr15:33162876-33162926	HNPCEpiC	eye:	n/a
19	chr15:33200866-33200916	SK-N-SH	brain:	n/a
20	chr15:33220732-33220782	HCF	heart:	n/a
21	chr15:33311906-33311956	HRE	kidney:	n/a
22	chr15:33235802-33235852	HRPEpiC	eye:	n/a
23	chr15:33165563-33165613	SKMC	muscle:	n/a
24	chr15:33162876-33162926	Hela-S3	cervix:	n/a
25	chr15:33178652-33178702	HepG2	liver:	n/a
26	chr15:33162876-33162926	ovcar-3	ovarian:	n/a
27	chr15:33311980-33312030	PFSK-1	brain:	n/a
28	chr15:33154262-33154312	U87	brain:	n/a
29	chr15:33191698-33191748	Hela-S3	cervix:	n/a
30	chr15:33311906-33311956	GM06990	blood:	n/a
31	chr15:33311031-33311081	HCPEpiC	choroid plexus:	n/a
32	chr15:33220732-33220782	LNCaP	prostate:	n/a
33	chr15:33211107-33211157	SK-N-MC	brain:	n/a
34	chr15:33320928-33320978	T-47D	breast:	n/a
35	chr15:33300472-33300522	AG04450	lung:	fetal
36	chr15:33307322-33307372	LNCaP	prostate:	n/a
37	chr15:33171339-33171389	HRCEpiC	kidney:	n/a
38	chr15:33179514-33179564	CMK	blood:	n/a
39	chr15:33200866-33200916	HRCEpiC	kidney:	n/a
40	chr15:33245281-33245331	HCM	heart:	n/a
41	chr15:33200866-33200916	PFSK-1	brain:	n/a
42	chr15:33307322-33307372	ECC-1	luminal epithelium:	n/a
43	chr15:33200866-33200916	HAEpiC	amniotic membrane:	n/a
44	chr15:33195247-33195297	GM12878	blood:	n/a
45	chr15:33245281-33245331	HIPEpiC	eye:	n/a
46	chr15:33245281-33245331	HL-60	blood:	n/a
47	chr15:33307322-33307372	Jurkat	blood:	n/a
48	chr15:33177867-33177917	HEEpiC	esophagus:	n/a
49	chr15:33310931-33310981	AG04449	skin:	fetal
50	chr15:33251279-33251329	BE2_C	brain:	n/a

(count:86 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr15:33312296..33313936-chr15:33357129..33359638,2	MCF-7	breast:
2	chr15:33326348..33328698-chr15:33332357..33334887,2	K562	blood:
3	chr15:33299875..33302830-chr15:33303027..33306565,4	MCF-7	breast:
4	chr15:33264185..33265845-chr15:33271129..33273337,2	MCF-7	breast:
5	chr15:33136574..33137426-chr15:33228228..33228738,2	K562	blood:
6	chr15:33276577..33278445-chr15:33292733..33295082,2	MCF-7	breast:
7	chr15:33313534..33314713-chr15:33367097..33367829,3	MCF-7	breast:
8	chr15:33321737..33324344-chr15:33359757..33362339,3	MCF-7	breast:
9	chr15:33194367..33197072-chr15:33201375..33203984,2	MCF-7	breast:
10	chr15:33203701..33205590-chr15:33205602..33207495,2	MCF-7	breast:
11	chr15:33237429..33239397-chr15:33241975..33243636,2	MCF-7	breast:
12	chr15:33298321..33300066-chr15:33361018..33362893,2	MCF-7	breast:
13	chr15:33191578..33193662-chr15:33205151..33207936,2	MCF-7	breast:
14	chr15:33317383..33320256-chr15:33356914..33360831,5	MCF-7	breast:
15	chr15:33159839..33162457-chr15:33167259..33169460,2	K562	blood:
16	chr15:33245362..33248334-chr15:33358852..33360940,3	MCF-7	breast:
17	chr15:33312479..33313997-chr15:33367303..33369166,2	MCF-7	breast:
18	chr15:33244172..33246376-chr15:33247943..33250082,2	K562	blood:
19	chr15:33289408..33292508-chr15:33359912..33362781,5	MCF-7	breast:
20	chr15:33305189..33307511-chr15:33365399..33368264,2	MCF-7	breast:
21	chr15:33310761..33317010-chr15:33354777..33361874,13	MCF-7	breast:
22	chr15:33340912..33343018-chr15:33358850..33361195,3	MCF-7	breast:
23	chr15:33177002..33179276-chr15:33196689..33199398,2	K562	blood:
24	chr15:33244592..33247228-chr15:33248722..33251718,2	MCF-7	breast:
25	chr15:33298305..33300128-chr15:33304629..33307307,2	MCF-7	breast:
26	chr15:33326108..33328482-chr15:33330757..33332929,2	MCF-7	breast:
27	chr15:33244172..33246376-chr15:33247943..33250082,2	K562	blood:
28	chr15:33203701..33205590-chr15:33205602..33207495,2	MCF-7	breast:
29	chr15:32954517..32955503-chr15:33228158..33229122,2	MCF-7	breast:
30	chr15:33299011..33299669-chr15:33424327..33425140,2	MCF-7	breast:
31	chr15:32943540..32944373-chr15:33286720..33287432,3	MCF-7	breast:
32	chr15:33300871..33303669-chr15:33360060..33362322,2	MCF-7	breast:
33	chr15:33326108..33328482-chr15:33330757..33332929,2	MCF-7	breast:
34	chr15:33312970..33316208-chr15:33320262..33322865,3	MCF-7	breast:
35	chr15:33313321..33315541-chr15:33363936..33365487,2	MCF-7	breast:
36	chr15:33287991..33290554-chr15:33293399..33295008,2	K562	blood:
37	chr15:32954026..32955488-chr15:33286759..33287801,5	K562	blood:
38	chr15:33191578..33193662-chr15:33205151..33207936,2	MCF-7	breast:
39	chr15:33191297..33193263-chr15:33193347..33195988,2	K562	blood:
40	chr15:33334051..33336029-chr15:33358668..33360282,2	MCF-7	breast:
41	chr15:33237429..33239397-chr15:33241975..33243636,2	MCF-7	breast:
42	chr15:33304810..33307499-chr15:33358975..33362023,4	MCF-7	breast:
43	chr15:33353607..33355965-chr15:33358462..33361026,3	MCF-7	breast:
44	chr15:33232993..33235695-chr15:33238081..33239940,2	K562	blood:
45	chr15:33276577..33278445-chr15:33292733..33295082,2	MCF-7	breast:
46	chr15:33312970..33316208-chr15:33320262..33322865,3	MCF-7	breast:
47	chr15:33264185..33265845-chr15:33271129..33273337,2	MCF-7	breast:
48	chr15:33264165..33266280-chr15:33277864..33279978,2	MCF-7	breast:
49	chr15:33244592..33247228-chr15:33248722..33251718,2	MCF-7	breast:
50	chr15:33232993..33235695-chr15:33238081..33239940,2	K562	blood:

No data

Variant related genes	Relation type
HNRNPA1P71	TF binding region
ENSG00000212415	TF binding region
FMN1	TF binding region
ENSG00000238342	TF binding region
HNRNPA1P71	CpG island
ENSG00000212415	CpG island
FMN1	CpG island
ENSG00000238342	CpG island
ENSG00000259686	chromatin interactions
ENSG00000248905	chromatin interactions

Extended variants
information (count: 10570 )
Associated
traits (count: 92 )

Variant overlapped rSNPs/rCNVs (count:10570 , 50 per page) page: 1 2 3 4 5 6 7 ... 212

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs544131134	chr15:33148059-33148060	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs367588758	chr15:33148119-33148120	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs34907509	chr15:33148129-33148130	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs375136100	chr15:33148131-33148132	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs10519756	chr15:33148207-33148208	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
6	rs147102052	chr15:33148209-33148210	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs541902787	chr15:33148219-33148220	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs560016605	chr15:33148245-33148246	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs184784729	chr15:33148295-33148296	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs527464265	chr15:33148299-33148300	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs552060846	chr15:33148312-33148313	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs570317863	chr15:33148321-33148322	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs190506530	chr15:33148337-33148338	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs181786288	chr15:33148402-33148403	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs568112258	chr15:33148404-33148405	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs552413729	chr15:33148415-33148416	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs535510003	chr15:33148464-33148465	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs554225424	chr15:33148523-33148524	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs566007432	chr15:33148568-33148569	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs539943847	chr15:33148596-33148597	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs558335617	chr15:33148599-33148600	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs576719105	chr15:33148603-33148604	Enhancers Weak transcription Strong transcription Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs570781699	chr15:33148664-33148665	Enhancers Weak transcription Strong transcription Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs186959192	chr15:33148697-33148698	Enhancers Weak transcription Strong transcription Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs574351080	chr15:33148712-33148713	Enhancers Weak transcription Strong transcription Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs189656202	chr15:33148716-33148717	Enhancers Weak transcription Strong transcription Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs560118216	chr15:33148737-33148738	Enhancers Weak transcription Strong transcription Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs138564185	chr15:33148867-33148868	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs545506571	chr15:33148897-33148898	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs563932395	chr15:33148911-33148912	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs531450437	chr15:33148914-33148915	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs549642842	chr15:33148949-33148950	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs553778492	chr15:33148976-33148977	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs561869893	chr15:33148996-33148997	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs529204388	chr15:33149004-33149005	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs540579543	chr15:33149010-33149011	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs547446808	chr15:33149054-33149055	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs8034124	chr15:33149059-33149060	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs8032931	chr15:33149087-33149088	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
40	rs551945721	chr15:33149133-33149134	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs570256276	chr15:33149141-33149142	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs75668978	chr15:33149152-33149153	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs556077850	chr15:33149161-33149162	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs574214730	chr15:33149169-33149170	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs370762225	chr15:33149170-33149171	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs374027347	chr15:33149172-33149173	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs367606290	chr15:33149175-33149176	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs541502365	chr15:33149186-33149187	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs371401743	chr15:33149187-33149188	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs1451888	chr15:33149196-33149197	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:92)

Disease	PMID	Source
HDAC8	0	CNVD
NIPBL	0	CNVD
RAD21	0	CNVD
SMC1A	0	CNVD
SMC3	0	CNVD
Ewing''s sarcoma	21437220	CNVD
Schizophrenia	19415332	CNVD
Breast cancer	22522925	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
Angelman syndrome	16183798	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Testicular germ cell tumor	18059402	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
Hodgkin''s lymphoma	18641027	CNVD
Melanoma	18172304	CNVD
Autism	17322880	CNVD
Prader-willi syndrome	19329560	CNVD
Autism	17999366	CNVD
Autism	17901113	CNVD
Neurodevelopmental disorder	17015230	CNVD
Autism	18414403	CNVD
Neurocytoma	17123091	CNVD
Mental retardation	18923513	CNVD
Colorectal cancer	16774939	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
Hodgkin''s lymphoma	17606441	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	21509527	CNVD
Acute myeloid leukemia	20729466	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Breast cancer	17133270	CNVD
Prostate cancer	16573809	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Multiple myeloma	20724749	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21858162	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	21785460	CNVD
Abnormal corpus callosum	21572526	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Autism	19204725	CNVD
Schizophrenia	19204725	CNVD
Schizophrenia	19149910	CNVD
Ovarian cancer	22174824	CNVD
Prostate cancer	18632612	CNVD
small cell lung cancer	20016488	CNVD
Autism	19521722	CNVD
Bipolar disorder	19114987	CNVD
Epilepsy	19521722	CNVD
Mental retardation	19521722	CNVD
Schizophrenia	19521646	CNVD
Autism	19050728	CNVD
Schizophrenia	19348701	CNVD
Schizophrenia	18668039	CNVD
Schizophrenia	18990708	CNVD
Schizophrenia	19571808	CNVD
Velocardiofacial syndrome	19329560	CNVD
Schizophrenia	19443537	CNVD
Epilepsy	20923578	CNVD
Autism	19955444	CNVD
Autism	20964600	CNVD
Schizophrenia	19955444	CNVD
Olfactory neuroblastoma	18408657	CNVD
Legius syndrome	19443465	CNVD
Holoprosencephaly	21359414	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	22286061	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:2664 , 50 per page) page: 1 2 3 4 5 6 7 ... 54

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:33096200-33154000	Weak transcription	Rectal Mucosa Donor 29	rectum
2	chr15:33096400-33159000	Weak transcription	Rectal Mucosa Donor 31	rectum
3	chr15:33118600-33159000	Weak transcription	Gastric	stomach
4	chr15:33131200-33153800	Weak transcription	Fetal Kidney	kidney
5	chr15:33131800-33164800	Weak transcription	Pancreas	Pancrea
6	chr15:33132000-33148600	Weak transcription	Stomach Mucosa	stomach
7	chr15:33132400-33154000	Weak transcription	Brain Inferior Temporal Lobe	brain
8	chr15:33132800-33154000	Weak transcription	Brain Angular Gyrus	brain
9	chr15:33133000-33148200	Weak transcription	Esophagus	oesophagus
10	chr15:33133000-33150400	Weak transcription	Duodenum Smooth Muscle	Duodenum
11	chr15:33135800-33148200	Weak transcription	Sigmoid Colon	Sigmoid Colon
12	chr15:33137800-33153600	Weak transcription	Fetal Thymus	thymus
13	chr15:33138800-33190600	Weak transcription	Thymus	Thymus
14	chr15:33139600-33190600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
15	chr15:33142600-33168200	Genic enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
16	chr15:33143200-33148600	Weak transcription	Placenta	Placenta
17	chr15:33143400-33150000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
18	chr15:33144000-33153600	Weak transcription	Primary monocytes fromperipheralblood	blood
19	chr15:33145800-33148600	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
20	chr15:33145800-33148600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
21	chr15:33146200-33148600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
22	chr15:33146200-33148600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
23	chr15:33146200-33149000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
24	chr15:33146600-33148200	Weak transcription	H1 Cell Line	embryonic stem cell
25	chr15:33146600-33148600	Weak transcription	Primary T helper cells fromperipheralblood	blood
26	chr15:33147000-33148800	Enhancers	HSMMtube	muscle
27	chr15:33147000-33191400	Weak transcription	Lung	lung
28	chr15:33147200-33149200	Enhancers	HUES64 Cell Line	embryonic stem cell
29	chr15:33147200-33150200	Enhancers	ES-I3 Cell Line	embryonic stem cell
30	chr15:33147400-33148600	Enhancers	NH-A	brain
31	chr15:33147400-33148600	Enhancers	NHDF-Ad	bronchial
32	chr15:33147400-33148800	Flanking Active TSS	A549	lung
33	chr15:33147400-33149200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
34	chr15:33147400-33149400	Enhancers	HUVEC	blood vessel
35	chr15:33147400-33150200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
36	chr15:33147400-33150400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
37	chr15:33147400-33150400	Enhancers	Osteobl	bone
38	chr15:33147400-33150600	Enhancers	HMEC	breast
39	chr15:33147400-33150800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
40	chr15:33147400-33150800	Enhancers	Muscle Satellite Cultured Cells	--
41	chr15:33147400-33150800	Enhancers	NHEK	skin
42	chr15:33147400-33151200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
43	chr15:33147400-33152200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
44	chr15:33147600-33149000	Enhancers	iPS-20b Cell Line	embryonic stem cell
45	chr15:33147600-33149400	Enhancers	HUES48 Cell Line	embryonic stem cell
46	chr15:33147600-33149400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
47	chr15:33147600-33149600	Strong transcription	Monocytes-CD14+_RO01746	blood
48	chr15:33147600-33150400	Genic enhancers	HSMM	muscle
49	chr15:33147600-33150400	Enhancers	NHLF	lung
50	chr15:33147800-33148400	Enhancers	Colon Smooth Muscle	Colon

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