Variant report

Variant	esv1812470
Chromosome Location	chr15:34685677-34889491
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2721)
CpG islands
(count:2930)
Chromatin interactive
region (count:59)
LncRNA
region (count:15)
Mature miRNA
region (count: 2)
miRNA target
sites (count:2)

(count:2721 , 50 per page) page: 1 2 3 4 5 6 7 ... 55

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	chr15:34869965-34870045	HepG2	liver:	n/a	n/a
3	ARID3A	chr15:34875226-34875237	K562	blood:	n/a	n/a
4	ARID3A	chr15:34880295-34880915	K562	blood:	n/a	n/a
5	ARID3A	chr15:34880209-34880840	HepG2	liver:	n/a	n/a
6	ARID3A	chr15:34731584-34731600	K562	blood:	n/a	n/a
7	ARID3A	chr15:34886706-34886742	K562	blood:	n/a	n/a
8	ATF1	chr15:34870112-34870339	K562	blood:	n/a	n/a
9	ATF1	chr15:34807442-34807640	K562	blood:	n/a	n/a
10	ATF1	chr15:34808283-34808324	K562	blood:	n/a	n/a
11	ATF1	chr15:34761374-34761389	K562	blood:	n/a	n/a
12	ATF1	chr15:34880295-34880819	K562	blood:	n/a	n/a
13	ATF2	chr15:34880257-34880906	GM12878	blood:	n/a	n/a
14	ATF2	chr15:34880485-34880875	H1-hESC	embryonic stem cell:	n/a	n/a
15	ATF2	chr15:34880089-34880894	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	chr15:34876822-34876846	K562	blood:	n/a	n/a
19	BACH1	chr15:34729369-34729390	H1-hESC	embryonic stem cell:	n/a	n/a
20	BATF	chr15:34695261-34695641	GM12878	blood:	n/a	n/a
21	BATF	chr15:34696017-34696728	GM12878	blood:	n/a	n/a
22	BATF	chr15:34808073-34808311	GM12878	blood:	n/a	n/a
23	BATF	chr15:34815930-34816436	GM12878	blood:	n/a	n/a
24	BATF	chr15:34842337-34842744	GM12878	blood:	n/a	n/a
25	BATF	chr15:34841482-34841862	GM12878	blood:	n/a	n/a
26	BATF	chr15:34695287-34695628	GM12878	blood:	n/a	n/a
27	BATF	chr15:34696116-34696523	GM12878	blood:	n/a	n/a
28	BATF	chr15:34762243-34762455	GM12878	blood:	n/a	n/a
29	BATF	chr15:34841508-34841849	GM12878	blood:	n/a	n/a
30	BATF	chr15:34842238-34842949	GM12878	blood:	n/a	n/a
31	BCL11A	chr15:34842236-34842734	GM12878	blood:	n/a	n/a
32	BCL11A	chr15:34816077-34816245	GM12878	blood:	n/a	chr15:34816149-34816162
33	BCL11A	chr15:34696015-34696513	GM12878	blood:	n/a	n/a
34	BCL11A	chr15:34875680-34875925	GM12878	blood:	n/a	chr15:34875720-34875733 chr15:34875761-34875774
35	BCL11A	chr15:34841554-34841859	GM12878	blood:	n/a	n/a
36	BCL11A	chr15:34695333-34695638	GM12878	blood:	n/a	n/a
37	BCLAF1	chr15:34874945-34875255	GM12878	blood:	n/a	n/a
38	BCLAF1	chr15:34729841-34730371	GM12878	blood:	n/a	n/a
39	BCLAF1	chr15:34875682-34876567	GM12878	blood:	n/a	chr15:34876318-34876331 chr15:34876075-34876088 chr15:34876322-34876335 chr15:34875720-34875733 chr15:34875761-34875774
40	BCLAF1	chr15:34729008-34729495	GM12878	blood:	n/a	chr15:34729354-34729367 chr15:34729445-34729458
41	BHLHE40	chr15:34875060-34875257	GM12878	blood:	n/a	n/a
42	BHLHE40	chr15:34875613-34876036	GM12878	blood:	n/a	chr15:34875930-34875946 chr15:34875736-34875752
43	BHLHE40	chr15:34729879-34730508	K562	blood:	n/a	n/a
44	BHLHE40	chr15:34869080-34869387	K562	blood:	n/a	n/a
45	BHLHE40	chr15:34729903-34730377	HepG2	liver:	n/a	n/a
46	BHLHE40	chr15:34754120-34754185	K562	blood:	n/a	n/a
47	BHLHE40	chr15:34808048-34808404	K562	blood:	n/a	n/a
48	BHLHE40	chr15:34875059-34875165	K562	blood:	n/a	n/a
49	BHLHE40	chr15:34807981-34808415	GM12878	blood:	n/a	n/a
50	BHLHE40	chr15:34729886-34730498	GM12878	blood:	n/a	n/a

(count:2930 , 50 per page) page: 1 2 3 4 5 6 7 ... 59

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:34875138-34875188	HUVEC	blood vessel:	n/a
2	chr15:34806349-34806399	IMR90	lung:	fetal
3	chr15:34875138-34875188	HUVEC	blood vessel:	n/a
4	chr15:34806349-34806399	IMR90	lung:	fetal
5	chr15:34875250-34875300	SAEC	small airway:	n/a
6	chr15:34880284-34880334	PrEC	prostate:	n/a
7	chr15:34729115-34729165	HRE	kidney:	n/a
8	chr15:34876295-34876345	HCT-116	colon:	n/a
9	chr15:34786594-34786644	Hepatocyte	liver:	n/a
10	chr15:34787400-34787450	RPTEC	kidney:	n/a
11	chr15:34872733-34872783	PFSK-1	brain:	n/a
12	chr15:34872733-34872783	Hela-S3	cervix:	n/a
13	chr15:34807221-34807271	HCT-116	colon:	n/a
14	chr15:34807221-34807271	SKMC	muscle:	n/a
15	chr15:34781969-34782019	A549	lung:	n/a
16	chr15:34875250-34875300	GM12878	blood:	n/a
17	chr15:34786594-34786644	PANC-1	pancreas:	n/a
18	chr15:34875138-34875188	Hela-S3	cervix:	n/a
19	chr15:34700272-34700322	GM12878	blood:	n/a
20	chr15:34791564-34791614	HUVEC	blood vessel:	n/a
21	chr15:34791564-34791614	GM12878	blood:	n/a
22	chr15:34875250-34875300	GM12891	blood:	n/a
23	chr15:34877407-34877457	RPTEC	kidney:	n/a
24	chr15:34875945-34875995	AG09309	skin:	n/a
25	chr15:34787420-34787470	NHDF-neo	bronchial:	n/a
26	chr15:34875117-34875167	ProgFib	skin:	n/a
27	chr15:34807143-34807193	HepG2	liver:	n/a
28	chr15:34787920-34787970	HRCEpiC	kidney:	n/a
29	chr15:34786594-34786644	HAEpiC	amniotic membrane:	n/a
30	chr15:34806810-34806860	PFSK-1	brain:	n/a
31	chr15:34787400-34787450	Caco-2	colon:	n/a
32	chr15:34782167-34782217	Caco-2	colon:	n/a
33	chr15:34787420-34787470	SK-N-MC	brain:	n/a
34	chr15:34791564-34791614	HIPEpiC	eye:	n/a
35	chr15:34781705-34781755	HEEpiC	esophagus:	n/a
36	chr15:34807143-34807193	SKMC	muscle:	n/a
37	chr15:34812400-34812450	HIPEpiC	eye:	n/a
38	chr15:34782167-34782217	ECC-1	luminal epithelium:	n/a
39	chr15:34788847-34788897	MCF-7	breast:	n/a
40	chr15:34787400-34787450	HAEpiC	amniotic membrane:	n/a
41	chr15:34788847-34788897	SKMC	muscle:	n/a
42	chr15:34806349-34806399	PANC-1	pancreas:	n/a
43	chr15:34875825-34875875	HPAEpiC	pulmonary alveolar:	n/a
44	chr15:34875945-34875995	ovcar-3	ovarian:	n/a
45	chr15:34876295-34876345	BE2_C	brain:	n/a
46	chr15:34874183-34874233	PFSK-1	brain:	n/a
47	chr15:34875937-34875987	HRE	kidney:	n/a
48	chr15:34875930-34875980	Jurkat	blood:	n/a
49	chr15:34785380-34785430	HRE	kidney:	n/a
50	chr15:34817982-34818032	SAEC	small airway:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr15:34729318..34730097-chr5:1799590..1800354,2	Hela-S3	cervix:
2	chr15:34761476..34764376-chr15:34768521..34770931,2	K562	blood:
3	chr15:34628679..34631455-chr15:34874185..34875808,2	K562	blood:
4	chr15:34873722..34878608-chr15:34878671..34882990,11	K562	blood:
5	chr15:34759701..34761289-chr15:34761464..34762969,2	K562	blood:
6	chr15:34351759..34355755-chr15:34876768..34880095,3	K562	blood:
7	chr15:34790342..34793794-chr15:34793900..34797346,3	K562	blood:
8	chr15:34790196..34793794-chr15:34794467..34797662,3	K562	blood:
9	chr15:34759701..34761289-chr15:34761464..34762969,2	K562	blood:
10	chr15:34867657..34871070-chr15:34876144..34878325,3	K562	blood:
11	chr15:34728587..34731061-chr15:34780506..34783189,2	K562	blood:
12	chr15:34513565..34517614-chr15:34877827..34881077,3	K562	blood:
13	chr15:34761476..34764376-chr15:34768521..34770931,2	K562	blood:
14	chr15:34786049..34786720-chr7:5632277..5632906,2	NB4	blood:
15	chr15:34633931..34636680-chr15:34728775..34730381,2	K562	blood:
16	chr15:34869058..34871895-chr15:34873883..34875893,3	K562	blood:
17	chr15:34867657..34871070-chr15:34876144..34878325,3	K562	blood:
18	chr15:34727095..34731466-chr15:34878887..34881950,4	K562	blood:
19	chr15:34770080..34772217-chr15:34772786..34775252,2	K562	blood:
20	chr15:34659566..34660339-chr15:34879136..34879733,2	MCF-7	breast:
21	chr15:34870217..34872096-chr15:35279333..35281998,2	K562	blood:
22	chr15:34770080..34772217-chr15:34772786..34775252,2	K562	blood:
23	chr15:34728587..34731061-chr15:34780506..34783189,2	K562	blood:
24	chr15:34875762..34878300-chr15:34879087..34881803,6	K562	blood:
25	chr15:34873722..34878608-chr15:34878671..34882990,11	K562	blood:
26	chr15:34790342..34793794-chr15:34793900..34797346,3	K562	blood:
27	chr15:34727667..34729400-chr15:34875206..34876777,2	K562	blood:
28	chr15:34726561..34729987-chr15:34871215..34874723,3	K562	blood:
29	chr15:34875152..34877762-chr15:34886558..34889393,2	MCF-7	breast:
30	chr15:34876102..34877627-chr15:34879229..34881136,2	MCF-7	breast:
31	chr15:34727885..34731466-chr15:34878887..34881950,4	K562	blood:
32	chr15:34783968..34786265-chr15:34799018..34801586,2	K562	blood:
33	chr15:34518743..34520763-chr15:34876016..34878611,2	MCF-7	breast:
34	chr15:34790196..34793794-chr15:34794467..34797662,3	K562	blood:
35	chr15:34769198..34772919-chr15:34774454..34777192,3	K562	blood:
36	chr15:34728587..34731061-chr15:34780506..34783189,3	K562	blood:
37	chr15:34774551..34776237-chr15:34779411..34782082,2	K562	blood:
38	chr15:34728531..34731203-chr15:34733693..34737649,5	K562	blood:
39	chr15:34720616..34722466-chr15:34725764..34728714,2	K562	blood:
40	chr15:34786054..34786721-chr7:5632299..5632821,2	HCT-116	colon:
41	chr15:34868472..34871070-chr15:34876144..34878325,2	K562	blood:
42	chr15:34769198..34772919-chr15:34774454..34777192,3	K562	blood:
43	chr15:34728131..34733225-chr15:34735717..34740218,7	K562	blood:
44	chr15:34762215..34765168-chr15:34878877..34880750,2	K562	blood:
45	chr15:34783968..34786265-chr15:34799018..34801586,2	K562	blood:
46	chr15:34875762..34878300-chr15:34879087..34881803,6	K562	blood:
47	chr15:34868472..34871070-chr15:34876144..34878325,2	K562	blood:
48	chr15:34727581..34729084-chr15:34874171..34876472,2	MCF-7	breast:
49	chr15:34658082..34661057-chr15:34874863..34877414,3	MCF-7	breast:
50	chr15:34330963..34332496-chr15:34876229..34877827,2	K562	blood:

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

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

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
ENSG00000260639	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
ENSG00000260639	CpG island
HNRNPLP2	CpG island
GOLGA8B	CpG island
ENSG00000171421	chromatin interactions
ENSG00000169857	chromatin interactions
ENSG00000140199	chromatin interactions
ENSG00000075618	chromatin interactions
ENSG00000215252	chromatin interactions
ENSG00000182117	chromatin interactions
ENSG00000184507	chromatin interactions
ENSG00000175265	chromatin interactions
ENSG00000128463	chromatin interactions
ENSG00000198146	chromatin interactions
ENSG00000176454	chromatin interactions
ENSG00000259917	chromatin interactions

Extended variants
information (count: 5880 )
Associated
traits (count: 69 )

Variant overlapped rSNPs/rCNVs (count:5880 , 50 per page) page: 1 2 3 4 5 6 7 ... 118

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs62018279	chr15:34685685-34685686	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs559620152	chr15:34685776-34685777	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs571843194	chr15:34685798-34685799	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs539268906	chr15:34685906-34685907	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs348318	chr15:34686789-34686790	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs62018280	chr15:34686861-34686862	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs62018281	chr15:34686960-34686961	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs532775304	chr15:34687019-34687020	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs62018282	chr15:34687089-34687090	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs347870	chr15:34687357-34687358	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs138900416	chr15:34687504-34687505	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs62018283	chr15:34687591-34687592	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs62018284	chr15:34687843-34687844	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs574170524	chr15:34688185-34688186	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs347872	chr15:34688609-34688610	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs62018286	chr15:34688989-34688990	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs142765346	chr15:34689325-34689326	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs147297767	chr15:34689334-34689335	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs557663033	chr15:34689454-34689455	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs576052140	chr15:34689485-34689486	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs536239643	chr15:34689519-34689520	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs554909475	chr15:34689571-34689572	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs62018287	chr15:34689615-34689616	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs573157622	chr15:34689682-34689683	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs540693146	chr15:34689849-34689850	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs565052960	chr15:34689850-34689851	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs577400943	chr15:34689888-34689889	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs544833144	chr15:34689897-34689898	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs563239558	chr15:34689901-34689902	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs530874926	chr15:34689957-34689958	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs202149269	chr15:34689971-34689972	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs147318884	chr15:34690090-34690091	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs140302180	chr15:34690091-34690092	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs528098806	chr15:34690120-34690121	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs551341247	chr15:34690314-34690315	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs546657570	chr15:34690373-34690374	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs563610447	chr15:34690384-34690385	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs571392380	chr15:34690392-34690393	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs539229730	chr15:34690591-34690592	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs144159590	chr15:34690629-34690630	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs551234356	chr15:34690633-34690634	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs569481984	chr15:34690646-34690647	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs200035598	chr15:34690657-34690658	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs371969724	chr15:34690679-34690680	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs347873	chr15:34690798-34690799	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs201652669	chr15:34691037-34691038	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs145843448	chr15:34691211-34691212	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs138144152	chr15:34691244-34691245	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs554983917	chr15:34691254-34691255	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs566822643	chr15:34691255-34691256	Weak transcription	n/a	n/a	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:2205 , 50 per page) page: 1 2 3 4 5 6 7 ... 45

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:34662800-34723600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
2	chr15:34667200-34691600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
3	chr15:34685200-34686000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
4	chr15:34689600-34689800	Enhancers	Primary T cells fromperipheralblood	blood
5	chr15:34689600-34690400	Enhancers	Primary hematopoietic stem cells short term culture	blood
6	chr15:34689600-34690400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
7	chr15:34689600-34690400	Enhancers	Primary T helper cells PMA-I stimulated	--
8	chr15:34689600-34690400	Enhancers	NHEK	skin
9	chr15:34689600-34691200	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
10	chr15:34689600-34691200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
11	chr15:34689800-34690600	Weak transcription	Primary T cells fromperipheralblood	blood
12	chr15:34695200-34722600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
13	chr15:34695400-34699400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
14	chr15:34706000-34710600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
15	chr15:34706800-34724200	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
16	chr15:34707800-34710600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
17	chr15:34709000-34721800	Weak transcription	GM12878-XiMat	blood
18	chr15:34709000-34724200	Weak transcription	Fetal Stomach	stomach
19	chr15:34709200-34715400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
20	chr15:34709200-34715800	Weak transcription	Fetal Muscle Trunk	muscle
21	chr15:34709200-34721800	Weak transcription	Stomach Smooth Muscle	stomach
22	chr15:34709400-34718200	Weak transcription	Fetal Muscle Leg	muscle
23	chr15:34709400-34720200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
24	chr15:34709600-34724200	Weak transcription	Hela-S3	cervix
25	chr15:34709600-34728000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
26	chr15:34709800-34728600	Weak transcription	Gastric	stomach
27	chr15:34710200-34718200	Weak transcription	Brain Anterior Caudate	brain
28	chr15:34710400-34724400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
29	chr15:34710600-34710800	Enhancers	H1 Cell Line	embryonic stem cell
30	chr15:34710600-34710800	Weak transcription	Primary T cells from cord blood	blood
31	chr15:34710600-34710800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
32	chr15:34710600-34710800	Weak transcription	Duodenum Mucosa	Duodenum
33	chr15:34710600-34711000	Enhancers	HUES6 Cell Line	embryonic stem cell
34	chr15:34710600-34711000	Enhancers	iPS-20b Cell Line	embryonic stem cell
35	chr15:34710600-34711000	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
36	chr15:34710600-34711200	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
37	chr15:34710600-34711200	Enhancers	Primary T cells fromperipheralblood	blood
38	chr15:34710600-34711200	Genic enhancers	Primary hematopoietic stem cells short term culture	blood
39	chr15:34710600-34711200	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
40	chr15:34710800-34711000	Enhancers	Primary T cells from cord blood	blood
41	chr15:34710800-34711000	Enhancers	Primary T helper naive cells fromperipheralblood	blood
42	chr15:34710800-34711000	Enhancers	Primary T helper cells PMA-I stimulated	--
43	chr15:34710800-34711000	Enhancers	Duodenum Mucosa	Duodenum
44	chr15:34710800-34711200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
45	chr15:34710800-34711200	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
46	chr15:34710800-34716000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
47	chr15:34711000-34720200	Weak transcription	Primary T helper cells PMA-I stimulated	--
48	chr15:34711000-34722000	Weak transcription	Primary T cells from cord blood	blood
49	chr15:34711000-34723800	Weak transcription	Duodenum Mucosa	Duodenum
50	chr15:34711000-34724400	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--

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