Variant report

Variant	nsv1044270
Chromosome Location	chr15:77534919-77611256
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr15:77574341-77574376	K562	blood:	n/a	n/a
2	ARID3A	chr15:77574443-77575153	HepG2	liver:	n/a	n/a
3	ARID3A	chr15:77598099-77599185	K562	blood:	n/a	n/a
4	ARID3A	chr15:77586248-77586518	HepG2	liver:	n/a	n/a
5	ARID3A	chr15:77585572-77585679	K562	blood:	n/a	n/a
6	BACH1	chr15:77598380-77598705	K562	blood:	n/a	n/a
7	BACH1	chr15:77559153-77559386	H1-hESC	embryonic stem cell:	n/a	n/a
8	BACH1	chr15:77574640-77575108	H1-hESC	embryonic stem cell:	n/a	chr15:77574731-77574745
9	BHLHE40	chr15:77598630-77598824	K562	blood:	n/a	n/a
10	CEBPB	chr15:77581561-77581805	A549	lung:	n/a	chr15:77581652-77581663 chr15:77581652-77581665 chr15:77581652-77581665
11	CEBPB	chr15:77587890-77588137	A549	lung:	n/a	n/a
12	CEBPB	chr15:77577701-77577947	A549	lung:	n/a	chr15:77577814-77577823 chr15:77577812-77577823
13	CEBPB	chr15:77603379-77603699	A549	lung:	n/a	chr15:77603554-77603567 chr15:77603554-77603565 chr15:77603554-77603567 chr15:77603555-77603566
14	CEBPB	chr15:77547734-77548064	IMR90	lung:	n/a	chr15:77547908-77547919
15	CEBPB	chr15:77577724-77577924	Hela-S3	cervix:	n/a	chr15:77577814-77577823 chr15:77577812-77577823
16	CEBPB	chr15:77603328-77603755	A549	lung:	n/a	chr15:77603554-77603567 chr15:77603554-77603565 chr15:77603554-77603567 chr15:77603555-77603566
17	CEBPB	chr15:77581603-77581739	K562	blood:	n/a	chr15:77581652-77581663 chr15:77581652-77581665 chr15:77581652-77581665
18	CEBPB	chr15:77604090-77604233	HepG2	liver:	n/a	n/a
19	CEBPB	chr15:77581534-77581794	IMR90	lung:	n/a	chr15:77581652-77581663 chr15:77581652-77581665 chr15:77581652-77581665
20	CEBPB	chr15:77547747-77548074	Hela-S3	cervix:	n/a	chr15:77547908-77547919
21	CEBPB	chr15:77547698-77548119	A549	lung:	n/a	chr15:77547908-77547919
22	CEBPB	chr15:77603375-77603734	K562	blood:	n/a	chr15:77603554-77603567 chr15:77603554-77603565 chr15:77603554-77603567 chr15:77603555-77603566
23	CEBPB	chr15:77608802-77609159	IMR90	lung:	n/a	n/a
24	CEBPB	chr15:77603434-77603663	H1-hESC	embryonic stem cell:	n/a	chr15:77603554-77603567 chr15:77603554-77603565 chr15:77603554-77603567 chr15:77603555-77603566
25	CEBPB	chr15:77547734-77548069	HepG2	liver:	n/a	chr15:77547908-77547919
26	CEBPB	chr15:77580077-77580250	K562	blood:	n/a	n/a
27	CEBPB	chr15:77604066-77604298	HepG2	liver:	n/a	n/a
28	CEBPB	chr15:77587814-77588227	IMR90	lung:	n/a	n/a
29	CEBPB	chr15:77577695-77577957	IMR90	lung:	n/a	chr15:77577814-77577823 chr15:77577812-77577823
30	CEBPB	chr15:77547746-77548072	A549	lung:	n/a	chr15:77547908-77547919
31	CEBPB	chr15:77581543-77581794	HepG2	liver:	n/a	chr15:77581652-77581663 chr15:77581652-77581665 chr15:77581652-77581665
32	CEBPB	chr15:77603402-77603735	Hela-S3	cervix:	n/a	chr15:77603554-77603567 chr15:77603554-77603565 chr15:77603554-77603567 chr15:77603555-77603566
33	CEBPB	chr15:77603377-77603740	HepG2	liver:	n/a	chr15:77603554-77603567 chr15:77603554-77603565 chr15:77603554-77603567 chr15:77603555-77603566
34	CEBPB	chr15:77603375-77603725	IMR90	lung:	n/a	chr15:77603554-77603567 chr15:77603554-77603565 chr15:77603554-77603567 chr15:77603555-77603566
35	CEBPB	chr15:77547740-77548098	K562	blood:	n/a	chr15:77547908-77547919
36	CEBPB	chr15:77547764-77548057	H1-hESC	embryonic stem cell:	n/a	chr15:77547908-77547919
37	CEBPB	chr15:77603453-77603666	MCF-7	breast:	n/a	chr15:77603554-77603567 chr15:77603554-77603565 chr15:77603554-77603567 chr15:77603555-77603566
38	CEBPB	chr15:77577696-77577953	HepG2	liver:	n/a	chr15:77577814-77577823 chr15:77577812-77577823
39	CEBPB	chr15:77603356-77603717	MCF-7	breast:	n/a	chr15:77603554-77603567 chr15:77603554-77603565 chr15:77603554-77603567 chr15:77603555-77603566
40	CTCF	chr15:77604097-77604167	H1-hESC	embryonic stem cell:	n/a	n/a
41	CTCF	chr15:77590006-77590080	MCF-7	breast:	n/a	n/a
42	CTCF	chr15:77604020-77604170	GM12874	blood:	n/a	n/a
43	CTCF	chr15:77604107-77604165	A549	lung:	n/a	n/a
44	CTCF	chr15:77567239-77567276	GM10248	blood:	n/a	n/a
45	CTCF	chr15:77590004-77590093	MCF-7	breast:	n/a	n/a
46	CTCF	chr15:77603983-77604261	HepG2	liver:	n/a	n/a
47	CTCF	chr15:77604980-77605130	AG10803	skin:	n/a	n/a
48	CTCF	chr15:77604180-77604330	A549	lung:	n/a	n/a
49	CTCF	chr15:77604096-77604242	GM12878	blood:	n/a	n/a
50	CTCF	chr15:77604044-77604223	MCF-7	breast:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:77570797-77570847	HPAEpiC	pulmonary alveolar:	n/a
2	chr15:77570797-77570847	HPAEpiC	pulmonary alveolar:	n/a
3	chr15:77577621-77577671	HCT-116	colon:	n/a
4	chr15:77577621-77577671	HRPEpiC	eye:	n/a
5	chr15:77570797-77570847	ProgFib	skin:	n/a
6	chr15:77599761-77599811	SAEC	small airway:	n/a
7	chr15:77577533-77577583	HCPEpiC	choroid plexus:	n/a
8	chr15:77601643-77601693	Hela-S3	cervix:	n/a
9	chr15:77577621-77577671	LNCaP	prostate:	n/a
10	chr15:77601643-77601693	GM19239	blood:	n/a
11	chr15:77599761-77599811	HCT-116	colon:	n/a
12	chr15:77570797-77570847	MCF10A-Er-Src	breast:	n/a
13	chr15:77570797-77570847	HEEpiC	esophagus:	n/a
14	chr15:77568977-77569027	GM12878	blood:	n/a
15	chr15:77599761-77599811	Caco-2	colon:	n/a
16	chr15:77568977-77569027	HNPCEpiC	eye:	n/a
17	chr15:77601643-77601693	HMEC	breast:	n/a
18	chr15:77574588-77574638	HCPEpiC	choroid plexus:	n/a
19	chr15:77570797-77570847	HRPEpiC	eye:	n/a
20	chr15:77577621-77577671	SKMC	muscle:	n/a
21	chr15:77577533-77577583	PANC-1	pancreas:	n/a
22	chr15:77568977-77569027	HPAEpiC	pulmonary alveolar:	n/a
23	chr15:77601643-77601693	HAEpiC	amniotic membrane:	n/a
24	chr15:77577655-77577705	HL-60	blood:	n/a
25	chr15:77574588-77574638	HNPCEpiC	eye:	n/a
26	chr15:77577491-77577541	AG10803	skin:	n/a
27	chr15:77577491-77577541	PANC-1	pancreas:	n/a
28	chr15:77577621-77577671	U87	brain:	n/a
29	chr15:77568977-77569027	AG04450	lung:	fetal
30	chr15:77577621-77577671	GM06990	blood:	n/a
31	chr15:77577491-77577541	SKMC	muscle:	n/a
32	chr15:77577491-77577541	GM12891	blood:	n/a
33	chr15:77574588-77574638	PANC-1	pancreas:	n/a
34	chr15:77599761-77599811	MCF10A-Er-Src	breast:	n/a
35	chr15:77577655-77577705	AoSMC	blood vessel:	n/a
36	chr15:77601643-77601693	NT2-D1	testis:	n/a
37	chr15:77574588-77574638	SKMC	muscle:	n/a
38	chr15:77577491-77577541	GM12892	blood:	n/a
39	chr15:77577655-77577705	HMEC	breast:	n/a
40	chr15:77570797-77570847	HMEC	breast:	n/a
41	chr15:77577491-77577541	LNCaP	prostate:	n/a
42	chr15:77577621-77577671	PrEC	prostate:	n/a
43	chr15:77577621-77577671	T-47D	breast:	n/a
44	chr15:77599761-77599811	T-47D	breast:	n/a
45	chr15:77577655-77577705	K562	blood:	n/a
46	chr15:77599761-77599811	ProgFib	skin:	n/a
47	chr15:77577655-77577705	NHBE	bronchial:	n/a
48	chr15:77577533-77577583	ovcar-3	ovarian:	n/a
49	chr15:77577621-77577671	NHDF-neo	bronchial:	n/a
50	chr15:77577655-77577705	Hela-S3	cervix:	n/a

No.	Distal block	Cell Line	Cell type
1	chr15:77533789..77536624-chr15:77711955..77714562,2	MCF-7	breast:
2	chr15:77580009..77582319-chr15:77583158..77585492,2	K562	blood:
3	chr15:77583990..77586060-chr15:77594625..77596162,2	K562	blood:
4	chr15:77587677..77589850-chr15:77710277..77712592,2	K562	blood:
5	chr15:77585431..77587225-chr15:77589534..77592219,2	K562	blood:
6	chr15:77546340..77548071-chr15:77585201..77587700,2	K562	blood:
7	chr15:77540244..77541923-chr15:77546088..77547627,2	K562	blood:
8	chr15:77573695..77576435-chr15:77580239..77581887,3	K562	blood:
9	chr15:77567760..77570371-chr15:77619185..77622166,2	MCF-7	breast:
10	chr15:77583990..77586060-chr15:77594625..77596162,2	K562	blood:
11	chr15:77587941..77589755-chr15:77592690..77595045,2	K562	blood:
12	chr15:76134586..76136640-chr15:77552323..77554009,2	MCF-7	breast:
13	chr15:77597221..77600603-chr15:77601241..77604606,4	K562	blood:
14	chr15:77567007..77569663-chr15:77575337..77577656,2	K562	blood:
15	chr15:77603476..77605050-chr15:77627091..77629724,2	K562	blood:
16	chr15:77585431..77587225-chr15:77589534..77592219,2	K562	blood:
17	chr15:77571666..77575195-chr15:77579317..77581859,3	K562	blood:
18	chr15:77362704..77365166-chr15:77609983..77612900,2	K562	blood:
19	chr15:77587941..77589755-chr15:77592690..77595045,2	K562	blood:
20	chr15:77571666..77575195-chr15:77579317..77581859,3	K562	blood:
21	chr15:77587934..77589441-chr15:77592568..77594190,2	K562	blood:
22	chr15:77597221..77600603-chr15:77601241..77604606,4	K562	blood:
23	chr15:77540244..77541923-chr15:77546088..77547627,2	K562	blood:
24	chr15:77576555..77578246-chr15:77578519..77580387,2	K562	blood:
25	chr15:77573695..77576435-chr15:77580239..77581887,3	K562	blood:
26	chr15:77587934..77589441-chr15:77592568..77594190,2	K562	blood:
27	chr15:77540284..77542372-chr15:77710056..77712718,2	K562	blood:
28	chr15:77543946..77545839-chr15:77577547..77579797,2	MCF-7	breast:
29	chr15:77580009..77582319-chr15:77583158..77585492,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PEAK1.1-1	chr15:77578764-77578846	XLOC_011535
2	lnc-PEAK1.1-1	chr15:77544841-77544868	NONHSAT047432
3	lnc-PEAK1.1-1	chr15:77576104-77576372	NONHSAT047435
4	lnc-PEAK1.1-1	chr15:77578765-77578846	NONHSAT047432
5	lnc-PEAK1.1-1	chr15:77577300-77577397	NONHSAT047431
6	lnc-PEAK1.1-1	chr15:77576225-77576372	NONHSAT047431
7	lnc-PEAK1.1-1	chr15:77577300-77577442	NONHSAT047435
8	lnc-PEAK1.1-1	chr15:77577300-77577420	NONHSAT047427
9	lnc-PEAK1.1-1	chr15:77578765-77578846	NONHSAT047431
10	lnc-PEAK1.1-1	chr15:77578765-77578846	NONHSAT047430
11	lnc-PEAK1.1-1	chr15:77578760-77578846	XLOC_011535
12	lnc-PEAK1.1-1	chr15:77544709-77544868	NONHSAT047427
13	lnc-PEAK1.1-1	chr15:77544764-77544868	NONHSAT047430
14	lnc-PEAK1.1-1	chr15:77576225-77576372	NONHSAT047432
15	lnc-PEAK1.1-1	chr15:77577300-77577420	NONHSAT047430
16	lnc-PEAK1.1-1	chr15:77577300-77577420	NONHSAT047432
17	lnc-PEAK1.1-1	chr15:77576225-77576372	NONHSAT047430
18	lnc-PEAK1.1-1	chr15:77544821-77544868	NONHSAT047431
19	lnc-PEAK1.1-1	chr15:77578765-77578846	NONHSAT047427

Variant related genes	Relation type
PEAK1	TF binding region
ENSG00000230459	TF binding region
PEAK1	CpG island
ENSG00000230459	CpG island
ENSG00000140382	chromatin interactions
ENSG00000173517	chromatin interactions
ENSG00000140367	chromatin interactions
ENSG00000140391	chromatin interactions
B4GALT1	miRNA target sites

Extended variants
information (count: 2758 )
Associated
traits (count: 53 )

Variant overlapped rSNPs/rCNVs (count:2758 , 50 per page) page: 1 2 3 4 5 6 7 ... 56

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs530753945	chr15:77535194-77535195	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs552443562	chr15:77535211-77535212	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs570604705	chr15:77535238-77535239	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs371990223	chr15:77535248-77535249	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs562513485	chr15:77535260-77535261	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs552714200	chr15:77535301-77535302	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs376270914	chr15:77535365-77535366	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs529902821	chr15:77535399-77535400	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs369225751	chr15:77535518-77535519	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs372751036	chr15:77535752-77535753	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs16968730	chr15:77535785-77535786	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
12	rs576377943	chr15:77535789-77535790	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs145016846	chr15:77535798-77535799	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs559207075	chr15:77535900-77535901	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs184840583	chr15:77535901-77535902	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs189350645	chr15:77535923-77535924	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs559960699	chr15:77535924-77535925	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs138708206	chr15:77535995-77535996	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs180993236	chr15:77536004-77536005	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs563184053	chr15:77536029-77536030	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs530530100	chr15:77536036-77536037	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs149381466	chr15:77536076-77536077	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs577812244	chr15:77536101-77536102	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs544863641	chr15:77536164-77536165	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs368825297	chr15:77536178-77536179	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs201836895	chr15:77536179-77536180	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs528340706	chr15:77536182-77536183	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs546418959	chr15:77536196-77536197	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs560901162	chr15:77536207-77536208	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs536388698	chr15:77536264-77536265	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs566829498	chr15:77536316-77536317	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs555043762	chr15:77536341-77536342	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs75888851	chr15:77536347-77536348	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs114693086	chr15:77536361-77536362	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs115253120	chr15:77536379-77536380	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs186208926	chr15:77536406-77536407	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs144587220	chr15:77536449-77536450	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs541729211	chr15:77536450-77536451	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs553641828	chr15:77536498-77536499	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs114091762	chr15:77536500-77536501	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs571483965	chr15:77536502-77536503	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs373439534	chr15:77536528-77536529	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs189496557	chr15:77536572-77536573	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs111658507	chr15:77536668-77536669	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs563406494	chr15:77536816-77536817	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs530488351	chr15:77536860-77536861	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs144717599	chr15:77536918-77536919	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs549893726	chr15:77536933-77536934	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs77411941	chr15:77536948-77536949	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs148141647	chr15:77536953-77536954	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:53)

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
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
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
small cell lung cancer	20016488	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:841 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:77492400-77544000	Weak transcription	Skeletal Muscle Female	skeletal muscle
2	chr15:77505800-77559400	Weak transcription	Psoas Muscle	Psoas
3	chr15:77508000-77543400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr15:77511200-77541800	Weak transcription	Sigmoid Colon	Sigmoid Colon
5	chr15:77517400-77559000	Weak transcription	Ovary	ovary
6	chr15:77517600-77543200	Weak transcription	HSMM	muscle
7	chr15:77517600-77545800	Weak transcription	Primary T helper cells fromperipheralblood	blood
8	chr15:77517800-77535400	Weak transcription	Brain Hippocampus Middle	brain
9	chr15:77517800-77544200	Weak transcription	NHLF	lung
10	chr15:77519400-77551800	Weak transcription	Duodenum Smooth Muscle	Duodenum
11	chr15:77519600-77551800	Weak transcription	Skeletal Muscle Male	skeletal muscle
12	chr15:77519800-77557200	Weak transcription	Rectal Mucosa Donor 31	rectum
13	chr15:77520000-77540000	Weak transcription	HUVEC	blood vessel
14	chr15:77520200-77578800	Weak transcription	Small Intestine	intestine
15	chr15:77523200-77544000	Weak transcription	Pancreas	Pancrea
16	chr15:77526400-77547600	Weak transcription	Liver	Liver
17	chr15:77526600-77538600	Weak transcription	Osteobl	bone
18	chr15:77527000-77559000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
19	chr15:77527000-77576200	Weak transcription	Monocytes-CD14+_RO01746	blood
20	chr15:77528200-77544200	Weak transcription	NH-A	brain
21	chr15:77528400-77553000	Weak transcription	Aorta	Aorta
22	chr15:77528600-77535600	Weak transcription	Fetal Brain Female	brain
23	chr15:77528600-77544000	Weak transcription	Placenta	Placenta
24	chr15:77528800-77559200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
25	chr15:77528800-77571400	Weak transcription	Right Ventricle	heart
26	chr15:77528800-77574400	Weak transcription	HepG2	liver
27	chr15:77528800-77577200	Weak transcription	Spleen	Spleen
28	chr15:77528800-77579200	Weak transcription	Brain Angular Gyrus	brain
29	chr15:77529000-77540800	Weak transcription	Cortex derived primary cultured neurospheres	brain
30	chr15:77529000-77543800	Weak transcription	HSMMtube	muscle
31	chr15:77529000-77544200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
32	chr15:77529000-77544200	Weak transcription	Primary B cells from peripheral blood	blood
33	chr15:77529000-77548600	Weak transcription	Gastric	stomach
34	chr15:77529200-77535400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
35	chr15:77529200-77538600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
36	chr15:77529200-77540600	Weak transcription	Primary neutrophils fromperipheralblood	blood
37	chr15:77529200-77540800	Weak transcription	Rectal Mucosa Donor 29	rectum
38	chr15:77529200-77541200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
39	chr15:77529200-77544000	Weak transcription	Duodenum Mucosa	Duodenum
40	chr15:77529200-77544000	Weak transcription	Fetal Lung	lung
41	chr15:77529200-77545800	Weak transcription	Primary monocytes fromperipheralblood	blood
42	chr15:77529200-77546400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
43	chr15:77529200-77546800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
44	chr15:77529200-77561400	Weak transcription	Primary T cells from cord blood	blood
45	chr15:77529400-77535400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
46	chr15:77529400-77536000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
47	chr15:77529400-77538400	Weak transcription	Fetal Intestine Small	intestine
48	chr15:77529400-77538600	Weak transcription	Fetal Stomach	stomach
49	chr15:77529400-77539800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
50	chr15:77529400-77540400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell

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