Variant report

Variant	esv1810277
Chromosome Location	chr15:34698843-34889691
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2652)
CpG islands
(count:2934)
Chromatin interactive
region (count:59)
LncRNA
region (count:15)
Mature miRNA
region (count: 2)
miRNA target
sites (count:2)

(count:2652 , 50 per page) page: 1 2 3 4 5 6 7 ... 54

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr15:34781246-34781587	K562	blood:	n/a	n/a
2	ARID3A	chr15:34880295-34880915	K562	blood:	n/a	n/a
3	ARID3A	chr15:34880209-34880840	HepG2	liver:	n/a	n/a
4	ARID3A	chr15:34869965-34870045	HepG2	liver:	n/a	n/a
5	ARID3A	chr15:34731584-34731600	K562	blood:	n/a	n/a
6	ARID3A	chr15:34875226-34875237	K562	blood:	n/a	n/a
7	ARID3A	chr15:34886706-34886742	K562	blood:	n/a	n/a
8	ATF1	chr15:34761374-34761389	K562	blood:	n/a	n/a
9	ATF1	chr15:34870112-34870339	K562	blood:	n/a	n/a
10	ATF1	chr15:34880295-34880819	K562	blood:	n/a	n/a
11	ATF1	chr15:34807442-34807640	K562	blood:	n/a	n/a
12	ATF1	chr15:34808283-34808324	K562	blood:	n/a	n/a
13	ATF2	chr15:34880089-34880894	GM12878	blood:	n/a	n/a
14	ATF2	chr15:34880485-34880875	H1-hESC	embryonic stem cell:	n/a	n/a
15	ATF2	chr15:34880257-34880906	GM12878	blood:	n/a	n/a
16	ATF3	chr15:34781262-34781502	K562	blood:	n/a	n/a
17	BACH1	chr15:34806578-34807213	H1-hESC	embryonic stem cell:	n/a	n/a
18	BACH1	chr15:34729369-34729390	H1-hESC	embryonic stem cell:	n/a	n/a
19	BACH1	chr15:34876822-34876846	K562	blood:	n/a	n/a
20	BATF	chr15:34815930-34816436	GM12878	blood:	n/a	n/a
21	BATF	chr15:34841482-34841862	GM12878	blood:	n/a	n/a
22	BATF	chr15:34762243-34762455	GM12878	blood:	n/a	n/a
23	BATF	chr15:34842238-34842949	GM12878	blood:	n/a	n/a
24	BATF	chr15:34808073-34808311	GM12878	blood:	n/a	n/a
25	BATF	chr15:34842337-34842744	GM12878	blood:	n/a	n/a
26	BATF	chr15:34841508-34841849	GM12878	blood:	n/a	n/a
27	BCL11A	chr15:34841554-34841859	GM12878	blood:	n/a	n/a
28	BCL11A	chr15:34816077-34816245	GM12878	blood:	n/a	chr15:34816149-34816162
29	BCL11A	chr15:34875680-34875925	GM12878	blood:	n/a	chr15:34875720-34875733 chr15:34875761-34875774
30	BCL11A	chr15:34842236-34842734	GM12878	blood:	n/a	n/a
31	BCLAF1	chr15:34729841-34730371	GM12878	blood:	n/a	n/a
32	BCLAF1	chr15:34729008-34729495	GM12878	blood:	n/a	chr15:34729354-34729367 chr15:34729445-34729458
33	BCLAF1	chr15:34874945-34875255	GM12878	blood:	n/a	n/a
34	BCLAF1	chr15:34875682-34876567	GM12878	blood:	n/a	chr15:34876318-34876331 chr15:34876075-34876088 chr15:34876322-34876335 chr15:34875720-34875733 chr15:34875761-34875774
35	BHLHE40	chr15:34729879-34730508	K562	blood:	n/a	n/a
36	BHLHE40	chr15:34875706-34876104	K562	blood:	n/a	chr15:34875930-34875946 chr15:34875736-34875752 chr15:34876078-34876094
37	BHLHE40	chr15:34728512-34728697	K562	blood:	n/a	n/a
38	BHLHE40	chr15:34806954-34807627	HepG2	liver:	n/a	chr15:34807373-34807389
39	BHLHE40	chr15:34875059-34875165	K562	blood:	n/a	n/a
40	BHLHE40	chr15:34806536-34807767	K562	blood:	n/a	chr15:34807373-34807389 chr15:34806722-34806738
41	BHLHE40	chr15:34804947-34805071	K562	blood:	n/a	chr15:34805006-34805019 chr15:34805002-34805023
42	BHLHE40	chr15:34781166-34781584	K562	blood:	n/a	n/a
43	BHLHE40	chr15:34806518-34806718	GM12878	blood:	n/a	n/a
44	BHLHE40	chr15:34807389-34807610	GM12878	blood:	n/a	n/a
45	BHLHE40	chr15:34729886-34730498	GM12878	blood:	n/a	n/a
46	BHLHE40	chr15:34875613-34876036	GM12878	blood:	n/a	chr15:34875930-34875946 chr15:34875736-34875752
47	BHLHE40	chr15:34729075-34729345	K562	blood:	n/a	n/a
48	BHLHE40	chr15:34875060-34875257	GM12878	blood:	n/a	n/a
49	BHLHE40	chr15:34754120-34754185	K562	blood:	n/a	n/a
50	BHLHE40	chr15:34880263-34880926	K562	blood:	n/a	n/a

(count:2934 , 50 per page) page: 1 2 3 4 5 6 7 ... 59

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:34817982-34818032	HPAEpiC	pulmonary alveolar:	n/a
2	chr15:34730071-34730121	A549	lung:	n/a
3	chr15:34781891-34781941	BJ	skin:	n/a
4	chr15:34781705-34781755	HAEpiC	amniotic membrane:	n/a
5	chr15:34782820-34782870	Hepatocyte	liver:	n/a
6	chr15:34807679-34807729	SK-N-SH	brain:	n/a
7	chr15:34817982-34818032	HPAEpiC	pulmonary alveolar:	n/a
8	chr15:34730071-34730121	A549	lung:	n/a
9	chr15:34781891-34781941	BJ	skin:	n/a
10	chr15:34781705-34781755	HAEpiC	amniotic membrane:	n/a
11	chr15:34782820-34782870	Hepatocyte	liver:	n/a
12	chr15:34807679-34807729	SK-N-SH	brain:	n/a
13	chr15:34817982-34818032	HAEpiC	amniotic membrane:	n/a
14	chr15:34807050-34807100	NH-A	brain:	n/a
15	chr15:34874862-34874912	HPAEpiC	pulmonary alveolar:	n/a
16	chr15:34807143-34807193	SK-N-SH_RA	brain:	n/a
17	chr15:34880284-34880334	MCF-7	breast:	n/a
18	chr15:34785380-34785430	GM06990	blood:	n/a
19	chr15:34874183-34874233	AG10803	skin:	n/a
20	chr15:34807221-34807271	SK-N-MC	brain:	n/a
21	chr15:34782820-34782870	PFSK-1	brain:	n/a
22	chr15:34872733-34872783	HRPEpiC	eye:	n/a
23	chr15:34787400-34787450	HCF	heart:	n/a
24	chr15:34730071-34730121	BJ	skin:	n/a
25	chr15:34791564-34791614	PrEC	prostate:	n/a
26	chr15:34806810-34806860	MCF10A-Er-Src	breast:	n/a
27	chr15:34875117-34875167	HNPCEpiC	eye:	n/a
28	chr15:34875250-34875300	GM12892	blood:	n/a
29	chr15:34817982-34818032	U87	brain:	n/a
30	chr15:34875930-34875980	PANC-1	pancreas:	n/a
31	chr15:34875250-34875300	ovcar-3	ovarian:	n/a
32	chr15:34876396-34876446	NB4	blood:	n/a
33	chr15:34700272-34700322	ovcar-3	ovarian:	n/a
34	chr15:34877407-34877457	MCF-7	breast:	n/a
35	chr15:34806810-34806860	T-47D	breast:	n/a
36	chr15:34875945-34875995	NHBE	bronchial:	n/a
37	chr15:34730071-34730121	NHBE	bronchial:	n/a
38	chr15:34880284-34880334	RPTEC	kidney:	n/a
39	chr15:34781969-34782019	HMEC	breast:	n/a
40	chr15:34877407-34877457	NHDF-neo	bronchial:	n/a
41	chr15:34876347-34876397	MCF-7	breast:	n/a
42	chr15:34781891-34781941	AG04449	skin:	fetal
43	chr15:34876283-34876333	HepG2	liver:	n/a
44	chr15:34876396-34876446	HEEpiC	esophagus:	n/a
45	chr15:34876283-34876333	HCT-116	colon:	n/a
46	chr15:34875138-34875188	PANC-1	pancreas:	n/a
47	chr15:34806349-34806399	SK-N-SH	brain:	n/a
48	chr15:34700272-34700322	LNCaP	prostate:	n/a
49	chr15:34876471-34876521	LNCaP	prostate:	n/a
50	chr15:34781891-34781941	PANC-1	pancreas:	n/a

(count:59 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr15:34632776..34635331-chr15:34879472..34881728,2	K562	blood:
2	chr15:34728131..34733225-chr15:34735717..34740218,7	K562	blood:
3	chr15:34727581..34729084-chr15:34874171..34876472,2	MCF-7	breast:
4	chr15:34873722..34878608-chr15:34878671..34882990,11	K562	blood:
5	chr15:34790196..34793794-chr15:34794467..34797662,3	K562	blood:
6	chr15:34658214..34660711-chr15:34806608..34809602,2	K562	blood:
7	chr15:34869058..34871895-chr15:34873883..34875893,3	K562	blood:
8	chr15:34658082..34661057-chr15:34874863..34877414,3	MCF-7	breast:
9	chr15:34728531..34731203-chr15:34733693..34737649,5	K562	blood:
10	chr15:34875152..34877762-chr15:34886558..34889393,2	MCF-7	breast:
11	chr15:34875762..34878300-chr15:34879087..34881803,6	K562	blood:
12	chr15:34729318..34730097-chr5:1799590..1800354,2	Hela-S3	cervix:
13	chr15:34868472..34871070-chr15:34876144..34878325,2	K562	blood:
14	chr15:34783968..34786265-chr15:34799018..34801586,2	K562	blood:
15	chr15:34518743..34520763-chr15:34876016..34878611,2	MCF-7	breast:
16	chr15:34727095..34731466-chr15:34878887..34881950,4	K562	blood:
17	chr15:34770080..34772217-chr15:34772786..34775252,2	K562	blood:
18	chr15:34875762..34878300-chr15:34879087..34881803,6	K562	blood:
19	chr15:34728587..34731061-chr15:34780506..34783189,2	K562	blood:
20	chr15:34868472..34871070-chr15:34876144..34878325,2	K562	blood:
21	chr15:34726561..34729987-chr15:34871215..34874723,3	K562	blood:
22	chr15:34659566..34660339-chr15:34879136..34879733,2	MCF-7	breast:
23	chr15:34761476..34764376-chr15:34768521..34770931,2	K562	blood:
24	chr15:34774551..34776237-chr15:34779411..34782082,2	K562	blood:
25	chr15:34786049..34786720-chr7:5632277..5632906,2	NB4	blood:
26	chr15:34727095..34731466-chr15:34878887..34881950,4	K562	blood:
27	chr15:34876102..34877627-chr15:34879229..34881136,2	MCF-7	breast:
28	chr15:34727885..34731466-chr15:34878887..34881950,4	K562	blood:
29	chr15:34330963..34332496-chr15:34876229..34877827,2	K562	blood:
30	chr15:34769198..34772919-chr15:34774454..34777192,3	K562	blood:
31	chr15:34727885..34731466-chr15:34878887..34881950,4	K562	blood:
32	chr15:34759701..34761289-chr15:34761464..34762969,2	K562	blood:
33	chr15:34727667..34729400-chr15:34875206..34876777,2	K562	blood:
34	chr15:34769198..34772919-chr15:34774454..34777192,3	K562	blood:
35	chr15:34774551..34776237-chr15:34779411..34782082,2	K562	blood:
36	chr15:34759701..34761289-chr15:34761464..34762969,2	K562	blood:
37	chr15:34633931..34636680-chr15:34728775..34730381,2	K562	blood:
38	chr15:34513565..34517614-chr15:34877827..34881077,3	K562	blood:
39	chr15:34786054..34786721-chr7:5632299..5632821,2	HCT-116	colon:
40	chr15:34790342..34793794-chr15:34793900..34797346,3	K562	blood:
41	chr15:34728587..34731061-chr15:34780506..34783189,3	K562	blood:
42	chr15:34659441..34662117-chr15:34875107..34877933,3	K562	blood:
43	chr15:34867657..34871070-chr15:34876144..34878325,3	K562	blood:
44	chr15:34790196..34793794-chr15:34794467..34797662,3	K562	blood:
45	chr15:34867657..34871070-chr15:34876144..34878325,3	K562	blood:
46	chr15:34770080..34772217-chr15:34772786..34775252,2	K562	blood:
47	chr15:34728587..34731061-chr15:34780506..34783189,2	K562	blood:
48	chr15:34873722..34878608-chr15:34878671..34882990,11	K562	blood:
49	chr15:34728066..34730668-chr15:34791069..34792682,2	K562	blood:
50	chr15:34783968..34786265-chr15:34799018..34801586,2	K562	blood:

(count:15 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GOLGA8B-1	chr15:34752685-34752950	uc_384_-
2	lnc-C15orf55-4	chr15:34752685-34752950	uc_384_+
3	lnc-GJD2-4	chr15:34845174-34845292	NONHSAT041596
4	lnc-GJD2-4	chr15:34843392-34843477	NONHSAT140232
5	lnc-GJD2-3	chr15:34874951-34875061	NONHSAT041597
6	lnc-LPCAT4-1	chr15:34698878-34699071	NONHSAT041586
7	lnc-GJD2-4	chr15:34845946-34846157	NONHSAT041596
8	lnc-GJD2-3	chr15:34858091-34858674	NONHSAT041597
9	lnc-LPCAT4-1	chr15:34699777-34699936	NONHSAT041586
10	lnc-GJD2-4	chr15:34867026-34867115	NONHSAT041596
11	lnc-LPCAT4-1	chr15:34720816-34721126	NONHSAT041586
12	lnc-GJD2-4	chr15:34845946-34846157	NONHSAT140232
13	lnc-GJD2-4	chr15:34845096-34845292	NONHSAT140232
14	lnc-GJD2-4	chr15:34873667-34873700	NONHSAT140232
15	lnc-GJD2-4	chr15:34875717-34875835	NONHSAT041596

miRNA name	Chromosome Location	mirBase accession
hsa-miR-1233-5p	chr15:34820548-34820569	MIMAT0022943_1
hsa-miR-1233-3p	chr15:34820491-34820510	MIMAT0005588_1

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	GOLGA8B	hsa-miR-15a-5p	chr15:34817527-34817548
2	GOLGA8B	hsa-miR-32-5p	chr15:34818291-34818311

Variant related genes	Relation type
MIR1233-2	TF binding region
ENSG00000259892	TF binding region
GOLGA8A	TF binding region
ENSG00000261081	TF binding region
ENSG00000261559	TF binding region
HNRNPLP2	TF binding region
GOLGA8B	TF binding region
MIR1233-2	CpG island
ENSG00000259892	CpG island
GOLGA8A	CpG island
ENSG00000261081	CpG island
ENSG00000261559	CpG island
HNRNPLP2	CpG island
GOLGA8B	CpG island
ENSG00000128463	chromatin interactions
ENSG00000184507	chromatin interactions
ENSG00000176454	chromatin interactions
ENSG00000215252	chromatin interactions
ENSG00000075618	chromatin interactions
ENSG00000175265	chromatin interactions
ENSG00000169857	chromatin interactions
ENSG00000198146	chromatin interactions
ENSG00000259917	chromatin interactions
ENSG00000171421	chromatin interactions
ENSG00000182117	chromatin interactions
ENSG00000140199	chromatin interactions

Extended variants
information (count: 5713 )
Associated
traits (count: 69 )

Variant overlapped rSNPs/rCNVs (count:5713 , 50 per page) page: 1 2 3 4 5 6 7 ... 115

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs375649980	chr15:34698887-34698888	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
2	rs535530825	chr15:34698909-34698910	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
3	rs547890771	chr15:34698949-34698950	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
4	rs566636858	chr15:34698950-34698951	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
5	rs534011161	chr15:34699006-34699007	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
6	rs368585651	chr15:34699381-34699382	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs112854206	chr15:34699444-34699445	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs372007211	chr15:34699449-34699450	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs375102923	chr15:34699755-34699756	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs62018291	chr15:34700001-34700002	Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
11	rs367713488	chr15:34700286-34700287	Weak transcription	TF binding region CpG island	2 gene(s)	Overlapped CNVs	n/a
12	rs77092095	chr15:34700297-34700298	Weak transcription	TF binding region CpG island	2 gene(s)	Overlapped CNVs	n/a
13	rs371205018	chr15:34700373-34700374	Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
14	rs201455393	chr15:34700808-34700809	Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
15	rs151045682	chr15:34700816-34700817	Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
16	rs202104272	chr15:34700852-34700853	Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
17	rs558869311	chr15:34700853-34700854	Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
18	rs577257490	chr15:34700867-34700868	Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
19	rs537832970	chr15:34700870-34700871	Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
20	rs555845523	chr15:34700893-34700894	Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
21	rs369278143	chr15:34701203-34701204	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs371506109	chr15:34701248-34701249	Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
23	rs527805903	chr15:34701253-34701254	Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
24	rs372055416	chr15:34701275-34701276	Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
25	rs75522640	chr15:34701293-34701294	Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
26	rs574379119	chr15:34701298-34701299	Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
27	rs79902072	chr15:34701312-34701313	Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
28	rs541534448	chr15:34701377-34701378	Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
29	rs62018292	chr15:34701385-34701386	Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
30	rs201937116	chr15:34701396-34701397	Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
31	rs372180359	chr15:34701482-34701483	Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
32	rs410397	chr15:34701498-34701499	Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
33	rs374954367	chr15:34701595-34701596	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs367266	chr15:34701614-34701615	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs401767	chr15:34701622-34701623	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs431030	chr15:34701641-34701642	Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
37	rs572292229	chr15:34701796-34701797	Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
38	rs546016991	chr15:34701799-34701800	Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
39	rs564427752	chr15:34701841-34701842	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs143252354	chr15:34701867-34701868	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs531842705	chr15:34701874-34701875	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs61741726	chr15:34701914-34701915	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs544096247	chr15:34701935-34701936	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs561902932	chr15:34701942-34701943	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs148922122	chr15:34701977-34701978	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs1692061	chr15:34702035-34702036	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs143712422	chr15:34702083-34702084	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs151052544	chr15:34702170-34702171	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs142424567	chr15:34702185-34702186	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs146863285	chr15:34702203-34702204	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:69)

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
Acute lymphoblastic leukemia	18458336	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
lymphocytic leukemia	21291569	CNVD

Chromatin state (count:2195 , 50 per page) page: 1 2 3 4 5 6 7 ... 44

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:34662800-34723600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
2	chr15:34695200-34722600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
3	chr15:34695400-34699400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
4	chr15:34706000-34710600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
5	chr15:34706800-34724200	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
6	chr15:34707800-34710600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr15:34709000-34721800	Weak transcription	GM12878-XiMat	blood
8	chr15:34709000-34724200	Weak transcription	Fetal Stomach	stomach
9	chr15:34709200-34715400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
10	chr15:34709200-34715800	Weak transcription	Fetal Muscle Trunk	muscle
11	chr15:34709200-34721800	Weak transcription	Stomach Smooth Muscle	stomach
12	chr15:34709400-34718200	Weak transcription	Fetal Muscle Leg	muscle
13	chr15:34709400-34720200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
14	chr15:34709600-34724200	Weak transcription	Hela-S3	cervix
15	chr15:34709600-34728000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
16	chr15:34709800-34728600	Weak transcription	Gastric	stomach
17	chr15:34710200-34718200	Weak transcription	Brain Anterior Caudate	brain
18	chr15:34710400-34724400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
19	chr15:34710600-34710800	Enhancers	H1 Cell Line	embryonic stem cell
20	chr15:34710600-34710800	Weak transcription	Primary T cells from cord blood	blood
21	chr15:34710600-34710800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
22	chr15:34710600-34710800	Weak transcription	Duodenum Mucosa	Duodenum
23	chr15:34710600-34711000	Enhancers	HUES6 Cell Line	embryonic stem cell
24	chr15:34710600-34711000	Enhancers	iPS-20b Cell Line	embryonic stem cell
25	chr15:34710600-34711000	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
26	chr15:34710600-34711200	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
27	chr15:34710600-34711200	Enhancers	Primary T cells fromperipheralblood	blood
28	chr15:34710600-34711200	Genic enhancers	Primary hematopoietic stem cells short term culture	blood
29	chr15:34710600-34711200	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
30	chr15:34710800-34711000	Enhancers	Primary T cells from cord blood	blood
31	chr15:34710800-34711000	Enhancers	Primary T helper naive cells fromperipheralblood	blood
32	chr15:34710800-34711000	Enhancers	Primary T helper cells PMA-I stimulated	--
33	chr15:34710800-34711000	Enhancers	Duodenum Mucosa	Duodenum
34	chr15:34710800-34711200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
35	chr15:34710800-34711200	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
36	chr15:34710800-34716000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
37	chr15:34711000-34720200	Weak transcription	Primary T helper cells PMA-I stimulated	--
38	chr15:34711000-34722000	Weak transcription	Primary T cells from cord blood	blood
39	chr15:34711000-34723800	Weak transcription	Duodenum Mucosa	Duodenum
40	chr15:34711000-34724400	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
41	chr15:34711000-34726800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
42	chr15:34711200-34718000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
43	chr15:34711200-34721800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
44	chr15:34711200-34724000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
45	chr15:34711200-34727800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
46	chr15:34711600-34713200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
47	chr15:34711600-34728600	Weak transcription	H9 Cell Line	embryonic stem cell
48	chr15:34711800-34724400	Weak transcription	HSMMtube	muscle
49	chr15:34712000-34722000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
50	chr15:34712000-34727800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood

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