Variant report

Variant	nsv1040053
Chromosome Location	chr15:76197988-76314542
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1165)
CpG islands
(count:857)
Chromatin interactive
region (count:81)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:3)

(count:1165 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr15:76305159-76305311	K562	blood:	n/a	n/a
2	ARID3A	chr15:76214100-76214463	K562	blood:	n/a	n/a
3	ARID3A	chr15:76222206-76222367	K562	blood:	n/a	n/a
4	ARID3A	chr15:76304405-76304909	K562	blood:	n/a	n/a
5	ATF1	chr15:76214159-76214601	K562	blood:	n/a	n/a
6	ATF1	chr15:76208798-76208847	K562	blood:	n/a	n/a
7	BACH1	chr15:76232998-76233284	K562	blood:	n/a	n/a
8	BACH1	chr15:76304558-76304885	K562	blood:	n/a	n/a
9	BACH1	chr15:76201756-76201909	K562	blood:	n/a	n/a
10	BACH1	chr15:76223369-76223448	K562	blood:	n/a	n/a
11	BCL11A	chr15:76238344-76238511	GM12878	blood:	n/a	n/a
12	BCL3	chr15:76235462-76236031	A549	lung:	n/a	n/a
13	BCL3	chr15:76236159-76237297	A549	lung:	n/a	chr15:76236250-76236259
14	BHLHE40	chr15:76304627-76304947	A549	lung:	n/a	n/a
15	BHLHE40	chr15:76311751-76311967	K562	blood:	n/a	n/a
16	BHLHE40	chr15:76214218-76214547	K562	blood:	n/a	n/a
17	BHLHE40	chr15:76304585-76305004	K562	blood:	n/a	n/a
18	BRCA1	chr15:76198161-76198162	H1-hESC	embryonic stem cell:	n/a	n/a
19	CEBPB	chr15:76258369-76258827	IMR90	lung:	n/a	n/a
20	CEBPB	chr15:76258358-76258798	A549	lung:	n/a	n/a
21	CEBPB	chr15:76226630-76226773	A549	lung:	n/a	n/a
22	CEBPB	chr15:76253654-76254005	Hela-S3	cervix:	n/a	chr15:76253826-76253835 chr15:76253826-76253835 chr15:76253824-76253837 chr15:76253826-76253835
23	CEBPB	chr15:76253646-76254010	IMR90	lung:	n/a	chr15:76253826-76253835 chr15:76253826-76253835 chr15:76253824-76253837 chr15:76253826-76253835
24	CEBPB	chr15:76278357-76278728	Hela-S3	cervix:	n/a	n/a
25	CEBPB	chr15:76298785-76299034	K562	blood:	n/a	chr15:76298947-76298958 chr15:76298948-76298957
26	CEBPB	chr15:76220972-76221332	A549	lung:	n/a	n/a
27	CEBPB	chr15:76253590-76254108	A549	lung:	n/a	chr15:76253826-76253835 chr15:76253826-76253835 chr15:76253824-76253837 chr15:76253826-76253835
28	CEBPB	chr15:76253675-76253956	H1-hESC	embryonic stem cell:	n/a	chr15:76253826-76253835 chr15:76253826-76253835 chr15:76253824-76253837 chr15:76253826-76253835
29	CEBPB	chr15:76241350-76241551	H1-hESC	embryonic stem cell:	n/a	chr15:76241438-76241449
30	CEBPB	chr15:76226003-76226203	K562	blood:	n/a	chr15:76226114-76226125
31	CEBPB	chr15:76241304-76241563	K562	blood:	n/a	chr15:76241438-76241449
32	CEBPB	chr15:76241325-76241525	Hela-S3	cervix:	n/a	chr15:76241438-76241449
33	CEBPB	chr15:76295482-76295656	K562	blood:	n/a	n/a
34	CEBPB	chr15:76304480-76304890	K562	blood:	n/a	n/a
35	CEBPB	chr15:76253603-76254088	MCF-7	breast:	n/a	chr15:76253826-76253835 chr15:76253826-76253835 chr15:76253824-76253837 chr15:76253826-76253835
36	CEBPB	chr15:76241253-76241608	HepG2	liver:	n/a	chr15:76241438-76241449
37	CEBPB	chr15:76298744-76299140	ECC-1	luminal epithelium:	n/a	chr15:76298947-76298958 chr15:76298948-76298957
38	CEBPB	chr15:76277193-76277346	Hela-S3	cervix:	n/a	chr15:76277241-76277252
39	CEBPB	chr15:76241290-76241577	IMR90	lung:	n/a	chr15:76241438-76241449
40	CEBPB	chr15:76241268-76241609	A549	lung:	n/a	chr15:76241438-76241449
41	CEBPB	chr15:76226077-76226217	IMR90	lung:	n/a	chr15:76226114-76226125
42	CEBPB	chr15:76277232-76277321	HepG2	liver:	n/a	chr15:76277241-76277252
43	CEBPB	chr15:76237928-76238718	IMR90	lung:	n/a	n/a
44	CEBPB	chr15:76298780-76299109	IMR90	lung:	n/a	chr15:76298947-76298958 chr15:76298948-76298957
45	CEBPB	chr15:76253639-76254005	HepG2	liver:	n/a	chr15:76253826-76253835 chr15:76253826-76253835 chr15:76253824-76253837 chr15:76253826-76253835
46	CEBPB	chr15:76298817-76299045	HepG2	liver:	n/a	chr15:76298947-76298958 chr15:76298948-76298957
47	CEBPB	chr15:76298753-76299143	Hela-S3	cervix:	n/a	chr15:76298947-76298958 chr15:76298948-76298957
48	CEBPB	chr15:76253603-76254009	MCF-7	breast:	n/a	chr15:76253826-76253835 chr15:76253826-76253835 chr15:76253824-76253837 chr15:76253826-76253835
49	CEBPB	chr15:76305541-76305650	K562	blood:	n/a	n/a
50	CEBPB	chr15:76298767-76299136	HepG2	liver:	n/a	chr15:76298947-76298958 chr15:76298948-76298957

(count:857 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:76218542-76218592	Caco-2	colon:	n/a
2	chr15:76287483-76287533	HRPEpiC	eye:	n/a
3	chr15:76304843-76304893	HUVEC	blood vessel:	n/a
4	chr15:76218542-76218592	Caco-2	colon:	n/a
5	chr15:76287483-76287533	HRPEpiC	eye:	n/a
6	chr15:76304843-76304893	HUVEC	blood vessel:	n/a
7	chr15:76225808-76225858	AG04449	skin:	fetal
8	chr15:76225330-76225380	HRPEpiC	eye:	n/a
9	chr15:76304531-76304581	GM12892	blood:	n/a
10	chr15:76304796-76304846	AG04450	lung:	fetal
11	chr15:76304546-76304596	Hela-S3	cervix:	n/a
12	chr15:76200166-76200216	HCT-116	colon:	n/a
13	chr15:76225808-76225858	NHBE	bronchial:	n/a
14	chr15:76222477-76222527	CMK	blood:	n/a
15	chr15:76304865-76304915	HRE	kidney:	n/a
16	chr15:76304531-76304581	NT2-D1	testis:	n/a
17	chr15:76287483-76287533	U87	brain:	n/a
18	chr15:76222477-76222527	K562	blood:	n/a
19	chr15:76218542-76218592	GM12878	blood:	n/a
20	chr15:76304796-76304846	SK-N-MC	brain:	n/a
21	chr15:76225330-76225380	MCF10A-Er-Src	breast:	n/a
22	chr15:76304865-76304915	HIPEpiC	eye:	n/a
23	chr15:76225330-76225380	ECC-1	luminal epithelium:	n/a
24	chr15:76218542-76218592	GM19239	blood:	n/a
25	chr15:76218542-76218592	HIPEpiC	eye:	n/a
26	chr15:76225330-76225380	LNCaP	prostate:	n/a
27	chr15:76225808-76225858	Hela-S3	cervix:	n/a
28	chr15:76304531-76304581	HPAEpiC	pulmonary alveolar:	n/a
29	chr15:76297890-76297940	SKMC	muscle:	n/a
30	chr15:76226687-76226737	SK-N-SH_RA	brain:	n/a
31	chr15:76222477-76222527	AoSMC	blood vessel:	n/a
32	chr15:76225808-76225858	RPTEC	kidney:	n/a
33	chr15:76304546-76304596	ovcar-3	ovarian:	n/a
34	chr15:76304531-76304581	AG09309	skin:	n/a
35	chr15:76297890-76297940	HPAEpiC	pulmonary alveolar:	n/a
36	chr15:76287483-76287533	SAEC	small airway:	n/a
37	chr15:76225330-76225380	HNPCEpiC	eye:	n/a
38	chr15:76304796-76304846	HEEpiC	esophagus:	n/a
39	chr15:76225808-76225858	PANC-1	pancreas:	n/a
40	chr15:76214616-76214666	MCF10A-Er-Src	breast:	n/a
41	chr15:76304843-76304893	ProgFib	skin:	n/a
42	chr15:76225330-76225380	U87	brain:	n/a
43	chr15:76304865-76304915	BE2_C	brain:	n/a
44	chr15:76222477-76222527	Jurkat	blood:	n/a
45	chr15:76304546-76304596	GM19239	blood:	n/a
46	chr15:76218542-76218592	SAEC	small airway:	n/a
47	chr15:76225330-76225380	PFSK-1	brain:	n/a
48	chr15:76225330-76225380	NH-A	brain:	n/a
49	chr15:76218542-76218592	HCM	heart:	n/a
50	chr15:76297890-76297940	HCF	heart:	n/a

(count:81 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr12:98909260..98909777-chr15:76304548..76305292,2	Hela-S3	cervix:
2	chr15:76133681..76139746-chr15:76193985..76199740,23	MCF-7	breast:
3	chr15:76273857..76276988-chr15:76280414..76283734,4	K562	blood:
4	chr1:121484265..121485133-chr15:76258560..76259558,2	MCF-7	breast:
5	chr15:76194745..76198135-chr15:76223912..76227637,3	MCF-7	breast:
6	chr15:76277087..76279426-chr15:76280170..76283503,3	K562	blood:
7	chr15:76225604..76228102-chr15:76229975..76232639,2	MCF-7	breast:
8	chr15:76231213..76235489-chr15:76235646..76238510,7	K562	blood:
9	chr15:76234349..76236125-chr15:76276845..76279711,2	K562	blood:
10	chr15:76273857..76276988-chr15:76280414..76283734,4	K562	blood:
11	chr15:76273577..76275608-chr15:76284248..76285874,2	K562	blood:
12	chr15:76196710..76199163-chr15:76204144..76205756,2	MCF-7	breast:
13	chr15:76102059..76103151-chr15:76213899..76214766,4	MCF-7	breast:
14	chr15:76230088..76234622-chr15:76234992..76238934,7	K562	blood:
15	chr15:76194745..76198135-chr15:76223912..76227637,3	MCF-7	breast:
16	chr15:76042074..76044891-chr15:76197743..76199352,2	K562	blood:
17	chr15:76196519..76198808-chr15:76210180..76211825,2	MCF-7	breast:
18	chr15:76230095..76231887-chr15:76232023..76234158,2	K562	blood:
19	chr15:76134186..76138083-chr15:76192925..76200499,13	K562	blood:
20	chr15:76220909..76222483-chr15:76431367..76432547,6	MCF-7	breast:
21	chr15:76231213..76235489-chr15:76235646..76238510,7	K562	blood:
22	chr15:76211169..76212903-chr15:76216124..76218574,2	K562	blood:
23	chr15:76198419..76200279-chr15:76206976..76209395,2	MCF-7	breast:
24	chr15:76230095..76231887-chr15:76232023..76234158,2	K562	blood:
25	chr15:76235823..76238133-chr15:76240535..76242101,2	K562	blood:
26	chr15:76256479..76258531-chr15:76292949..76295388,2	K562	blood:
27	chr15:76195569..76197871-chr15:76205442..76207733,2	K562	blood:
28	chr15:76221299..76222193-chr15:76443491..76444002,2	MCF-7	breast:
29	chr15:76194938..76197869-chr15:76206105..76209095,4	MCF-7	breast:
30	chr15:76228613..76230905-chr15:76232150..76235048,3	MCF-7	breast:
31	chr15:76197909..76200277-chr15:76201455..76203414,2	MCF-7	breast:
32	chr1:121484292..121485419-chr15:76258560..76259078,3	MCF-7	breast:
33	chr15:76135493..76137289-chr15:76195431..76198634,3	MCF-7	breast:
34	chr15:76240565..76242407-chr15:76245195..76247516,2	K562	blood:
35	chr15:76043391..76046153-chr15:76197743..76199339,2	K562	blood:
36	chr15:76195569..76197871-chr15:76204617..76208764,4	K562	blood:
37	chr15:76196239..76198362-chr15:76207161..76208693,2	MCF-7	breast:
38	chr15:76240565..76242407-chr15:76245195..76247516,2	K562	blood:
39	chr15:76196519..76198808-chr15:76210180..76211825,2	MCF-7	breast:
40	chr15:76238474..76241248-chr15:76241585..76243858,2	K562	blood:
41	chr15:76100272..76101901-chr15:76213487..76215015,2	MCF-7	breast:
42	chr15:76235823..76238133-chr15:76240535..76242101,2	K562	blood:
43	chr15:76301816..76304344-chr15:76313829..76315747,2	K562	blood:
44	chr15:76206066..76207638-chr15:76207776..76210184,2	K562	blood:
45	chr15:76256479..76258531-chr15:76292949..76295388,2	K562	blood:
46	chr15:76197876..76200191-chr15:76201024..76203742,3	K562	blood:
47	chr15:76273577..76275608-chr15:76284248..76285874,2	K562	blood:
48	chr15:76195364..76197764-chr15:76200093..76201997,3	K562	blood:
49	chr15:76286599..76288465-chr15:76289865..76291672,2	K562	blood:
50	chr15:76195434..76197797-chr15:76257193..76258703,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-NRG4-1	chr15:76235913-76235995	NONHSAT047388
2	lnc-NRG4-1	chr15:76238099-76238186	NONHSAT047388
3	lnc-NRG4-1	chr15:76228310-76228651	NONHSAT047388
4	lnc-NRG4-1	chr15:76228310-76228651	NONHSAT047387
5	lnc-NRG4-1	chr15:76234979-76235113	NONHSAT047387

No data

(count:3 , 50 per page) page: 1

No.	miRNA target gene	miRNA name	Chromosome Location
1	FBXO22	hsa-miR-1	chr15:76222492-76222513
2	FBXO22	hsa-miR-1	chr15:76225787-76225793
3	FBXO22	hsa-miR-1	chr15:76225772-76225794

Variant related genes	Relation type
ENSG00000260685	TF binding region
FBXO22	TF binding region
NRG4	TF binding region
ENSG00000260685	CpG island
FBXO22	CpG island
NRG4	CpG island
ENSG00000167196	chromatin interactions
ENSG00000260685	chromatin interactions
ENSG00000140367	chromatin interactions
ENSG00000169752	chromatin interactions
ENSG00000120802	chromatin interactions

Extended variants
information (count: 3223 )
Associated
traits (count: 56 )

Variant overlapped rSNPs/rCNVs (count:3223 , 50 per page) page: 1 2 3 4 5 6 7 ... 65

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs554195819	chr15:76198012-76198013	Genic enhancers Weak transcription Strong transcription Transcr. at gene 5' and 3' Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs574391541	chr15:76198021-76198022	Genic enhancers Weak transcription Strong transcription Transcr. at gene 5' and 3' Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs528361133	chr15:76198022-76198023	Genic enhancers Weak transcription Strong transcription Transcr. at gene 5' and 3' Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs76636379	chr15:76198065-76198066	Genic enhancers Weak transcription Strong transcription Transcr. at gene 5' and 3' Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs542272179	chr15:76198066-76198067	Genic enhancers Weak transcription Strong transcription Transcr. at gene 5' and 3' Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs560895903	chr15:76198090-76198091	Genic enhancers Weak transcription Strong transcription Transcr. at gene 5' and 3' Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs371755802	chr15:76198094-76198095	Genic enhancers Weak transcription Strong transcription Transcr. at gene 5' and 3' Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs575945531	chr15:76198166-76198167	Genic enhancers Weak transcription Strong transcription Transcr. at gene 5' and 3' Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs181602173	chr15:76198302-76198303	Genic enhancers Weak transcription Strong transcription Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs147574665	chr15:76198326-76198327	Genic enhancers Weak transcription Strong transcription Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs185324971	chr15:76198339-76198340	Genic enhancers Weak transcription Strong transcription Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs190124049	chr15:76198367-76198368	Genic enhancers Weak transcription Strong transcription Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs139502637	chr15:76198376-76198377	Genic enhancers Weak transcription Strong transcription Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs78531351	chr15:76198430-76198431	Strong transcription Weak transcription Transcr. at gene 5' and 3' Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs535259752	chr15:76198520-76198521	Strong transcription Weak transcription Transcr. at gene 5' and 3' Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs180852836	chr15:76198569-76198570	Strong transcription Weak transcription Transcr. at gene 5' and 3' Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs567696519	chr15:76198585-76198586	Strong transcription Weak transcription Transcr. at gene 5' and 3' Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs75552790	chr15:76198655-76198656	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs368069379	chr15:76198661-76198662	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs571386153	chr15:76198682-76198683	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs1699263	chr15:76198708-76198709	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
22	rs554307257	chr15:76198784-76198785	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs186257054	chr15:76198787-76198788	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs545857307	chr15:76198828-76198829	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs191922185	chr15:76198909-76198910	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs184164566	chr15:76199005-76199006	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs148868806	chr15:76199027-76199028	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs543424214	chr15:76199036-76199037	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs368080698	chr15:76199039-76199040	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs74024018	chr15:76199129-76199130	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs1699264	chr15:76199132-76199133	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs80197160	chr15:76199192-76199193	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs548524923	chr15:76199238-76199239	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs145456922	chr15:76199257-76199258	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs559207436	chr15:76199260-76199261	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs574621362	chr15:76199291-76199292	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs559450750	chr15:76199299-76199300	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs565345366	chr15:76199460-76199461	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs187982805	chr15:76199490-76199491	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs547668889	chr15:76199505-76199506	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs561593459	chr15:76199581-76199582	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs542145728	chr15:76199630-76199631	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs78909156	chr15:76199672-76199673	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs531623488	chr15:76199696-76199697	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs549736579	chr15:76199745-76199746	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs79022260	chr15:76199767-76199768	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs532427418	chr15:76199812-76199813	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs547572923	chr15:76199897-76199898	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs566304143	chr15:76199956-76199957	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs190505745	chr15:76200002-76200003	Strong transcription Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:56)

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
Breast cancer	21364760	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
Pancreatic cancer	17952125	CNVD
Renal cell carcinoma	21215367	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:1745 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:76195800-76198200	Active TSS	iPS-15b Cell Line	embryonic stem cell
2	chr15:76197000-76200600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr15:76197000-76200600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
4	chr15:76197000-76200600	Weak transcription	Left Ventricle	heart
5	chr15:76197000-76205800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr15:76197000-76206200	Weak transcription	Brain Cingulate Gyrus	brain
7	chr15:76197000-76210800	Weak transcription	Aorta	Aorta
8	chr15:76197000-76214600	Weak transcription	Small Intestine	intestine
9	chr15:76197200-76198000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
10	chr15:76197200-76198000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
11	chr15:76197200-76198000	Weak transcription	Primary B cells from cord blood	blood
12	chr15:76197200-76198000	Enhancers	Primary T helper naive cells from peripheral blood	blood
13	chr15:76197200-76198000	Enhancers	Colon Smooth Muscle	Colon
14	chr15:76197200-76198000	Enhancers	Fetal Brain Male	brain
15	chr15:76197200-76198000	Enhancers	Rectal Mucosa Donor 31	rectum
16	chr15:76197200-76198000	Enhancers	Skeletal Muscle Female	skeletal muscle
17	chr15:76197200-76198000	Enhancers	HUVEC	blood vessel
18	chr15:76197200-76198200	Enhancers	Primary T helper naive cells fromperipheralblood	blood
19	chr15:76197200-76198200	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
20	chr15:76197200-76198400	Enhancers	Primary T killer naive cells fromperipheralblood	blood
21	chr15:76197200-76200000	Weak transcription	Fetal Stomach	stomach
22	chr15:76197200-76200600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
23	chr15:76197200-76200600	Weak transcription	Fetal Intestine Small	intestine
24	chr15:76197200-76202200	Weak transcription	Fetal Lung	lung
25	chr15:76197200-76205400	Weak transcription	Primary neutrophils fromperipheralblood	blood
26	chr15:76197200-76205400	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
27	chr15:76197200-76205400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
28	chr15:76197200-76205400	Weak transcription	Brain Germinal Matrix	brain
29	chr15:76197200-76205400	Weak transcription	Rectal Smooth Muscle	rectum
30	chr15:76197200-76205600	Weak transcription	Ovary	ovary
31	chr15:76197200-76206000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
32	chr15:76197200-76206000	Weak transcription	Brain Angular Gyrus	brain
33	chr15:76197200-76206200	Weak transcription	Skeletal Muscle Male	skeletal muscle
34	chr15:76197200-76206600	Weak transcription	Thymus	Thymus
35	chr15:76197200-76216800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
36	chr15:76197200-76216800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
37	chr15:76197400-76198000	Transcr. at gene 5' and 3'	ES-I3 Cell Line	embryonic stem cell
38	chr15:76197400-76198000	Transcr. at gene 5' and 3'	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
39	chr15:76197400-76198000	Genic enhancers	Brain Inferior Temporal Lobe	brain
40	chr15:76197400-76198000	Flanking Active TSS	Hela-S3	cervix
41	chr15:76197400-76198200	Transcr. at gene 5' and 3'	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
42	chr15:76197400-76198200	Genic enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
43	chr15:76197400-76198200	Enhancers	Pancreatic Islets	Pancreatic Islet
44	chr15:76197400-76198200	Enhancers	Gastric	stomach
45	chr15:76197400-76198200	Genic enhancers	Sigmoid Colon	Sigmoid Colon
46	chr15:76197400-76198400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
47	chr15:76197400-76198400	Transcr. at gene 5' and 3'	HepG2	liver
48	chr15:76197400-76198400	Transcr. at gene 5' and 3'	HMEC	breast
49	chr15:76197400-76198600	Transcr. at gene 5' and 3'	H9 Derived Neuron Cultured Cells	ES cell derived
50	chr15:76197400-76198600	Transcr. at gene 5' and 3'	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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