Variant report

Variant	nsv456789
Chromosome Location	chr15:34034421-34426618
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:3549)
CpG islands
(count:2747)
Chromatin interactive
region (count:148)
LncRNA
region (count:16)
Mature miRNA
region (count: 0)
miRNA target
sites (count:13)

(count:3549 , 50 per page) page: 1 2 3 4 5 6 7 ... 71

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr15:34394020-34394474	K562	blood:	n/a	n/a
2	ARID3A	chr15:34402309-34402652	K562	blood:	n/a	n/a
3	ARID3A	chr15:34248257-34248412	K562	blood:	n/a	n/a
4	ARID3A	chr15:34353989-34354392	K562	blood:	n/a	n/a
5	ARID3A	chr15:34330215-34330630	HepG2	liver:	n/a	n/a
6	ARID3A	chr15:34248712-34248988	K562	blood:	n/a	n/a
7	ARID3A	chr15:34393681-34394773	HepG2	liver:	n/a	n/a
8	ARID3A	chr15:34403426-34403439	K562	blood:	n/a	n/a
9	ARID3A	chr15:34218510-34218807	HepG2	liver:	n/a	n/a
10	ARID3A	chr15:34204713-34204749	HepG2	liver:	n/a	n/a
11	ARID3A	chr15:34402362-34402600	HepG2	liver:	n/a	n/a
12	ARID3A	chr15:34354196-34354396	HepG2	liver:	n/a	n/a
13	ARID3A	chr15:34256399-34256618	K562	blood:	n/a	n/a
14	ARID3A	chr15:34425798-34426034	HepG2	liver:	n/a	n/a
15	ATF1	chr15:34248197-34248892	K562	blood:	n/a	n/a
16	ATF1	chr15:34102834-34102951	K562	blood:	n/a	n/a
17	ATF1	chr15:34339680-34340079	K562	blood:	n/a	n/a
18	ATF1	chr15:34144751-34144915	K562	blood:	n/a	n/a
19	ATF1	chr15:34393917-34394573	K562	blood:	n/a	n/a
20	ATF1	chr15:34258445-34258610	K562	blood:	n/a	n/a
21	ATF1	chr15:34372194-34372442	K562	blood:	n/a	n/a
22	ATF1	chr15:34071163-34071335	K562	blood:	n/a	n/a
23	ATF2	chr15:34414899-34415466	GM12878	blood:	n/a	n/a
24	ATF2	chr15:34393901-34394585	GM12878	blood:	n/a	n/a
25	ATF2	chr15:34393917-34394425	H1-hESC	embryonic stem cell:	n/a	n/a
26	ATF2	chr15:34393805-34394669	GM12878	blood:	n/a	n/a
27	ATF2	chr15:34393860-34394355	H1-hESC	embryonic stem cell:	n/a	n/a
28	ATF3	chr15:34393858-34394377	H1-hESC	embryonic stem cell:	n/a	n/a
29	ATF3	chr15:34393914-34394305	HepG2	liver:	n/a	n/a
30	ATF3	chr15:34393643-34394339	K562	blood:	n/a	n/a
31	ATF3	chr15:34393859-34394435	GM12878	blood:	n/a	n/a
32	ATF3	chr15:34339649-34340072	K562	blood:	n/a	n/a
33	ATF3	chr15:34393937-34394330	K562	blood:	n/a	n/a
34	ATF3	chr15:34393736-34394572	A549	lung:	n/a	n/a
35	ATF3	chr15:34393843-34394517	A549	lung:	n/a	n/a
36	ATF3	chr15:34393971-34394379	H1-hESC	embryonic stem cell:	n/a	n/a
37	ATF3	chr15:34394020-34394235	GM12878	blood:	n/a	n/a
38	ATF3	chr15:34393835-34394379	HepG2	liver:	n/a	n/a
39	BACH1	chr15:34339685-34339984	K562	blood:	n/a	n/a
40	BACH1	chr15:34394099-34394585	H1-hESC	embryonic stem cell:	n/a	n/a
41	BACH1	chr15:34330554-34331302	H1-hESC	embryonic stem cell:	n/a	n/a
42	BACH1	chr15:34152601-34152801	H1-hESC	embryonic stem cell:	n/a	n/a
43	BACH1	chr15:34127101-34127499	H1-hESC	embryonic stem cell:	n/a	n/a
44	BACH1	chr15:34391683-34391775	K562	blood:	n/a	n/a
45	BACH1	chr15:34394195-34394625	K562	blood:	n/a	n/a
46	BACH1	chr15:34060923-34060934	K562	blood:	n/a	n/a
47	BATF	chr15:34382088-34382251	GM12878	blood:	n/a	n/a
48	BATF	chr15:34394026-34394483	GM12878	blood:	n/a	chr15:34394119-34394132
49	BATF	chr15:34190306-34190556	GM12878	blood:	n/a	chr15:34190407-34190418
50	BATF	chr15:34331690-34332086	GM12878	blood:	n/a	n/a

(count:2747 , 50 per page) page: 1 2 3 4 5 6 7 ... 55

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:34333534-34333584	HL-60	blood:	n/a
2	chr15:34261172-34261222	HIPEpiC	eye:	n/a
3	chr15:34333534-34333584	HL-60	blood:	n/a
4	chr15:34261172-34261222	HIPEpiC	eye:	n/a
5	chr15:34394263-34394313	SKMC	muscle:	n/a
6	chr15:34393715-34393765	PANC-1	pancreas:	n/a
7	chr15:34394260-34394310	AG04450	lung:	fetal
8	chr15:34331198-34331248	AG10803	skin:	n/a
9	chr15:34260719-34260769	BE2_C	brain:	n/a
10	chr15:34330588-34330638	NT2-D1	testis:	n/a
11	chr15:34355300-34355350	HCPEpiC	choroid plexus:	n/a
12	chr15:34331198-34331248	GM19239	blood:	n/a
13	chr15:34376369-34376419	HEEpiC	esophagus:	n/a
14	chr15:34396248-34396298	ECC-1	luminal epithelium:	n/a
15	chr15:34331198-34331248	IMR90	lung:	fetal
16	chr15:34389967-34390017	HAEpiC	amniotic membrane:	n/a
17	chr15:34393959-34394009	GM06990	blood:	n/a
18	chr15:34158767-34158817	AG09319	gingival:	n/a
19	chr15:34394035-34394085	HNPCEpiC	eye:	n/a
20	chr15:34355300-34355350	K562	blood:	n/a
21	chr15:34331514-34331564	BJ	skin:	n/a
22	chr15:34332433-34332483	LNCaP	prostate:	n/a
23	chr15:34152971-34153021	BE2_C	brain:	n/a
24	chr15:34260956-34261006	HCPEpiC	choroid plexus:	n/a
25	chr15:34339800-34339850	NHDF-neo	bronchial:	n/a
26	chr15:34280002-34280052	Hepatocyte	liver:	n/a
27	chr15:34396328-34396378	NHDF-neo	bronchial:	n/a
28	chr15:34394376-34394426	Hela-S3	cervix:	n/a
29	chr15:34158767-34158817	NB4	blood:	n/a
30	chr15:34331198-34331248	HEEpiC	esophagus:	n/a
31	chr15:34331557-34331607	ovcar-3	ovarian:	n/a
32	chr15:34261172-34261222	T-47D	breast:	n/a
33	chr15:34331390-34331440	SK-N-SH	brain:	n/a
34	chr15:34394138-34394188	HEEpiC	esophagus:	n/a
35	chr15:34389967-34390017	HCPEpiC	choroid plexus:	n/a
36	chr15:34394218-34394268	HCPEpiC	choroid plexus:	n/a
37	chr15:34143840-34143890	HRCEpiC	kidney:	n/a
38	chr15:34394376-34394426	NH-A	brain:	n/a
39	chr15:34332433-34332483	SAEC	small airway:	n/a
40	chr15:34331198-34331248	H1-hESC	embryonic stem cell:	embryo
41	chr15:34396328-34396378	NH-A	brain:	n/a
42	chr15:34127219-34127269	SAEC	small airway:	n/a
43	chr15:34376369-34376419	SK-N-SH	brain:	n/a
44	chr15:34327794-34327844	MCF-7	breast:	n/a
45	chr15:34389967-34390017	SAEC	small airway:	n/a
46	chr15:34331390-34331440	AG04449	skin:	fetal
47	chr15:34331557-34331607	IMR90	lung:	fetal
48	chr15:34355300-34355350	HAEpiC	amniotic membrane:	n/a
49	chr15:34332433-34332483	HRE	kidney:	n/a
50	chr15:34394263-34394313	AG04450	lung:	fetal

(count:148 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr15:34402131..34404554-chr15:34408275..34409911,2	K562	blood:
2	chr15:34224044..34225662-chr15:34226786..34229394,2	MCF-7	breast:
3	chr15:34402458..34403052-chr15:34501962..34502479,2	MCF-7	breast:
4	chr15:34361453..34364220-chr15:34368679..34370797,2	K562	blood:
5	chr15:34308484..34310036-chr15:34321852..34323927,2	MCF-7	breast:
6	chr15:34392855..34396101-chr15:34515904..34518783,5	MCF-7	breast:
7	chr15:34314534..34316475-chr15:34330485..34333173,2	MCF-7	breast:
8	chr15:34030460..34032334-chr15:34033934..34035565,2	K562	blood:
9	chr15:34330374..34330923-chr15:34659512..34660213,2	K562	blood:
10	chr15:34402131..34404554-chr15:34408275..34409911,2	K562	blood:
11	chr15:34325247..34329253-chr15:34329844..34332256,3	MCF-7	breast:
12	chr15:34361453..34364220-chr15:34368679..34370797,2	K562	blood:
13	chr15:34391885..34395742-chr15:34500701..34502399,4	K562	blood:
14	chr15:34402115..34404646-chr15:34407237..34411184,3	K562	blood:
15	chr15:34401088..34402962-chr15:34501811..34503818,2	MCF-7	breast:
16	chr15:34397749..34399755-chr15:34409612..34411614,2	K562	blood:
17	chr15:34391943..34394373-chr15:34406757..34408689,2	K562	blood:
18	chr15:34330950..34333091-chr15:34501411..34503652,2	K562	blood:
19	chr15:34332870..34334555-chr15:34335095..34337616,2	MCF-7	breast:
20	chr15:34057550..34059117-chr15:34255937..34257253,6	MCF-7	breast:
21	chr15:34389075..34392114-chr15:34392453..34395895,3	K562	blood:
22	chr15:34389885..34392673-chr15:34392994..34394930,2	MCF-7	breast:
23	chr15:34402115..34404646-chr15:34407237..34411184,3	K562	blood:
24	chr15:34374878..34376788-chr15:34377498..34380301,3	K562	blood:
25	chr15:34391225..34395745-chr15:34498845..34504196,8	K562	blood:
26	chr15:34094725..34097105-chr15:34140341..34142261,2	K562	blood:
27	chr15:34402010..34402956-chr15:34659467..34660260,3	K562	blood:
28	chr15:34353917..34354774-chr15:34879983..34880925,3	MCF-7	breast:
29	chr15:34354339..34357870-chr15:34358322..34362266,6	K562	blood:
30	chr15:34101810..34104755-chr15:34112644..34114520,2	K562	blood:
31	chr15:34353900..34354754-chr15:34880301..34880822,2	K562	blood:
32	chr15:34027757..34028484-chr15:34286175..34286847,2	MCF-7	breast:
33	chr15:34331236..34333239-chr15:34415576..34418277,2	MCF-7	breast:
34	chr15:34299066..34301596-chr15:34326883..34329699,2	MCF-7	breast:
35	chr1:45987162..45987999-chr15:34330632..34331222,2	NB4	blood:
36	chr15:34215496..34217980-chr15:34219492..34221807,2	K562	blood:
37	chr15:34329343..34331465-chr15:34336277..34339020,2	MCF-7	breast:
38	chr15:34371878..34373674-chr15:34446162..34448935,2	K562	blood:
39	chr15:34376281..34379013-chr15:34384199..34386317,2	K562	blood:
40	chr15:34027979..34028642-chr15:34267350..34267863,2	MCF-7	breast:
41	chr15:34354339..34357870-chr15:34358322..34362266,6	K562	blood:
42	chr15:34351759..34355755-chr15:34876768..34880095,3	K562	blood:
43	chr15:34320977..34323643-chr15:34328767..34331333,2	MCF-7	breast:
44	chr15:34131010..34134235-chr15:34134372..34138936,4	K562	blood:
45	chr1:231003799..231004442-chr15:34330464..34331002,2	Hela-S3	cervix:
46	chr15:34410925..34412547-chr15:34416896..34419566,2	K562	blood:
47	chr15:34330614..34331132-chr22:21984221..21984750,2	NB4	blood:
48	chr15:34330893..34332620-chr15:34346063..34348142,2	MCF-7	breast:
49	chr15:34410925..34412547-chr15:34416896..34419566,2	K562	blood:
50	chr15:34393898..34395784-chr15:34415043..34417474,3	MCF-7	breast:

(count:16 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PGBD4-1	chr15:34283727-34284249	NONHSAT041560
2	lnc-CHRM5-1	chr15:34236644-34237538	l_1128_chr15:34188603-34237538_heart
3	lnc-CHRM5-1	chr15:34258907-34259306	l_1128_chr15:34188603-34237538_heart
4	lnc-C15orf24-3	chr15:34161849-34162094	NONHSAT041559
5	lnc-AVEN-2	chr15:34148514-34149010	ENSG00000259408.1
6	lnc-PGBD4-1	chr15:34282887-34283566	NONHSAT041560
7	lnc-C15orf24-1	chr15:34361591-34361954	NONHSAT041561
8	lnc-CHRM5-2	chr15:34128595-34129022	l_1127_chr15:34125499-34129001_testes
9	lnc-CHRM5-1	chr15:34188604-34188683	l_1128_chr15:34188603-34237538_heart
10	lnc-CHRM5-2	chr15:34125500-34125778	l_1127_chr15:34125499-34129001_testes
11	lnc-AVEN-2	chr15:34146115-34147146	NONHSAT041555
12	lnc-AVEN-2	chr15:34148514-34148786	NONHSAT041555
13	lnc-CHRM5-1	chr15:34259320-34259445	l_1128_chr15:34188603-34237538_heart
14	lnc-AVEN-1	chr15:34156958-34157026	ENSG00000259287.1
15	lnc-AVEN-1	chr15:34150918-34151295	ENSG00000259287.1
16	lnc-AVEN-2	chr15:34147101-34147146	ENSG00000259408.1

No data

(count:13 , 50 per page) page: 1

No.	miRNA target gene	miRNA name	Chromosome Location
1	RYR3	hsa-miR-26b-5p	chr15:34157779-34157799
2	AVEN	hsa-miR-30a-5p	chr15:34158513-34158534
3	AVEN	hsa-miR-30a-5p	chr15:34158519-34158512
4	AVEN	hsa-miR-98-5p	chr15:34158674-34158668
5	RYR3	hsa-miR-124-3p	chr15:34157961-34157980
6	RYR3	hsa-miR-124-3p	chr15:34157973-34157980
7	RYR3	hsa-miR-26b-5p	chr15:34158082-34158088
8	C15orf24	hsa-miR-192-5p	chr15:34376330-34376349
9	C15orf24	hsa-miR-192-5p	chr15:34376335-34376329
10	AVEN	hsa-miR-98-5p	chr15:34158668-34158687
11	AVEN	hsa-miR-30a-5p	chr15:34158531-34158553
12	C15orf24	hsa-miR-215-5p	chr15:34376335-34376329
13	C15orf24	hsa-miR-215-5p	chr15:34376330-34376349

Variant related genes	Relation type
ENSG00000259505	TF binding region
ENSG00000243094	TF binding region
PGBD4	TF binding region
ENSG00000259408	TF binding region
RYR3	TF binding region
EMC7	TF binding region
ENSG00000259287	TF binding region
CHRM5	TF binding region
AVEN	TF binding region
ENSG00000259505	CpG island
ENSG00000243094	CpG island
PGBD4	CpG island
ENSG00000259408	CpG island
RYR3	CpG island
EMC7	CpG island
ENSG00000259287	CpG island
CHRM5	CpG island
AVEN	CpG island
ENSG00000021776	chromatin interactions
ENSG00000182405	chromatin interactions
ENSG00000169857	chromatin interactions
ENSG00000140199	chromatin interactions
ENSG00000134153	chromatin interactions
ENSG00000103253	chromatin interactions
ENSG00000243094	chromatin interactions
ENSG00000180806	chromatin interactions
ENSG00000264395	chromatin interactions
ENSG00000128463	chromatin interactions
ENSG00000258738	chromatin interactions
ENSG00000258017	chromatin interactions
ENSG00000134152	chromatin interactions
ENSG00000161179	chromatin interactions
ENSG00000119280	chromatin interactions
ENSG00000123416	chromatin interactions
ENSG00000215252	chromatin interactions
ENSG00000176454	chromatin interactions
ENSG00000161847	chromatin interactions
ENSG00000198838	chromatin interactions
ENSG00000198604	chromatin interactions
ENSG00000173846	chromatin interactions
ENSG00000197757	chromatin interactions
ENSG00000117450	chromatin interactions
ENSG00000148335	chromatin interactions
ENSG00000259408	chromatin interactions

Extended variants
information (count: 16887 )
Associated
traits (count: 71 )

Variant overlapped rSNPs/rCNVs (count:16887 , 50 per page) page: 1 2 3 4 5 6 7 ... 338

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2288608	chr15:34034421-34034422	Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs2288609	chr15:34034446-34034447	Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs564820366	chr15:34034461-34034462	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs371935260	chr15:34034516-34034517	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs571010681	chr15:34034517-34034518	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs199944284	chr15:34034524-34034525	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs138414127	chr15:34034529-34034530	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs369786059	chr15:34034545-34034546	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs149242033	chr15:34034573-34034574	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs7165225	chr15:34034594-34034595	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs369629619	chr15:34034598-34034599	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs201310633	chr15:34034601-34034602	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs538327874	chr15:34034608-34034609	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs58775107	chr15:34034636-34034637	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs377219654	chr15:34034672-34034673	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs368987173	chr15:34034673-34034674	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs193112575	chr15:34034699-34034700	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs533750828	chr15:34034759-34034760	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs36115768	chr15:34034794-34034795	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs112810737	chr15:34034795-34034796	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs73379377	chr15:34034806-34034807	Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs577103931	chr15:34034809-34034810	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs544764470	chr15:34034811-34034812	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs55804668	chr15:34034817-34034818	Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs116507069	chr15:34034850-34034851	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs74005979	chr15:34034853-34034854	Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs138453532	chr15:34034856-34034857	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs116379145	chr15:34034866-34034867	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs34423282	chr15:34034873-34034874	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs56193977	chr15:34034945-34034946	Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs56089586	chr15:34034974-34034975	Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs11378841	chr15:34035004-34035005	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs376954992	chr15:34035006-34035007	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs55879601	chr15:34035007-34035008	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs201597942	chr15:34035016-34035017	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs4779642	chr15:34035036-34035037	Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs568597603	chr15:34035042-34035043	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs551919982	chr15:34035200-34035201	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs142979354	chr15:34035203-34035204	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs570403907	chr15:34035218-34035219	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs548121678	chr15:34035248-34035249	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs534655902	chr15:34035253-34035254	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs566663485	chr15:34035260-34035261	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs534136297	chr15:34035268-34035269	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs146111721	chr15:34035269-34035270	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs72715104	chr15:34035278-34035279	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs538020722	chr15:34035279-34035280	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs72715106	chr15:34035287-34035288	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs574844489	chr15:34035321-34035322	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs535226053	chr15:34035347-34035348	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:71)

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
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
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
Legius syndrome	19443465	CNVD
Holoprosencephaly	21359414	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	22286061	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Prader-willi syndrome	21504564	CNVD
Cancer	17440070	CNVD
Basal cell lymphoma	17053054	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Renal cell carcinoma	21215367	CNVD
Bipolar disorder	19114987	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:3968 , 50 per page) page: 1 2 3 4 5 6 7 ... 80

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:33993000-34034600	Weak transcription	Colon Smooth Muscle	Colon
2	chr15:34024200-34034800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
3	chr15:34025400-34035200	Weak transcription	Fetal Muscle Leg	muscle
4	chr15:34030400-34038000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
5	chr15:34030600-34038200	Weak transcription	Brain Cingulate Gyrus	brain
6	chr15:34030600-34038200	Weak transcription	Brain Inferior Temporal Lobe	brain
7	chr15:34030800-34034600	Weak transcription	Brain Substantia Nigra	brain
8	chr15:34030800-34035200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
9	chr15:34030800-34038200	Weak transcription	Brain Hippocampus Middle	brain
10	chr15:34030800-34040000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
11	chr15:34031000-34034600	Strong transcription	Aorta	Aorta
12	chr15:34031800-34034800	Weak transcription	Duodenum Smooth Muscle	Duodenum
13	chr15:34032400-34041000	Weak transcription	HUES6 Cell Line	embryonic stem cell
14	chr15:34033000-34035400	Weak transcription	Fetal Muscle Trunk	muscle
15	chr15:34034000-34034600	Weak transcription	Brain Anterior Caudate	brain
16	chr15:34034000-34034800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
17	chr15:34034200-34034800	Enhancers	Brain Germinal Matrix	brain
18	chr15:34034200-34035400	Enhancers	Fetal Brain Male	brain
19	chr15:34034200-34035400	Enhancers	Psoas Muscle	Psoas
20	chr15:34034200-34035600	Enhancers	Fetal Stomach	stomach
21	chr15:34034200-34035600	Enhancers	Skeletal Muscle Female	skeletal muscle
22	chr15:34034200-34035600	Enhancers	HSMMtube	muscle
23	chr15:34034200-34035800	Enhancers	Skeletal Muscle Male	skeletal muscle
24	chr15:34034400-34034800	Enhancers	Fetal Lung	lung
25	chr15:34034400-34035000	Enhancers	Rectal Smooth Muscle	rectum
26	chr15:34034400-34035000	Enhancers	Stomach Smooth Muscle	stomach
27	chr15:34034400-34035400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
28	chr15:34034400-34035400	Enhancers	Cortex derived primary cultured neurospheres	brain
29	chr15:34034400-34035400	Enhancers	Fetal Brain Female	brain
30	chr15:34034400-34035600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
31	chr15:34034600-34034800	Enhancers	Brain Substantia Nigra	brain
32	chr15:34034600-34034800	Enhancers	Colon Smooth Muscle	Colon
33	chr15:34034600-34035200	Enhancers	Brain Anterior Caudate	brain
34	chr15:34034600-34035600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
35	chr15:34034600-34048600	Weak transcription	Aorta	Aorta
36	chr15:34034800-34035000	Enhancers	Fetal Kidney	kidney
37	chr15:34034800-34035400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
38	chr15:34034800-34035400	Enhancers	Duodenum Smooth Muscle	Duodenum
39	chr15:34034800-34035600	Strong transcription	Breast Myoepithelial Primary Cells	Breast
40	chr15:34034800-34038000	Weak transcription	Brain Substantia Nigra	brain
41	chr15:34034800-34042200	Weak transcription	Brain Germinal Matrix	brain
42	chr15:34034800-34050400	Weak transcription	Colon Smooth Muscle	Colon
43	chr15:34035000-34035400	Enhancers	Fetal Lung	lung
44	chr15:34035000-34035800	Weak transcription	Stomach Smooth Muscle	stomach
45	chr15:34035200-34035600	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
46	chr15:34035200-34036000	Genic enhancers	Fetal Muscle Leg	muscle
47	chr15:34035200-34038400	Weak transcription	Brain Anterior Caudate	brain
48	chr15:34035400-34035600	Bivalent Enhancer	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
49	chr15:34035400-34035800	Strong transcription	Fetal Muscle Trunk	muscle
50	chr15:34035400-34042200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain

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