Variant report

Variant	esv992827
Chromosome Location	chr15:34672823-34872439
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1834)
CpG islands
(count:1773)
Chromatin interactive
region (count:40)
LncRNA
region (count:12)
Mature miRNA
region (count: 4)
miRNA target
sites (count:2)

(count:1834 , 50 per page) page: 1 2 3 4 5 6 7 ... 37

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	chr15:34731584-34731600	K562	blood:	n/a	n/a
3	ARID3A	chr15:34869965-34870045	HepG2	liver:	n/a	n/a
4	ATF1	chr15:34870112-34870339	K562	blood:	n/a	n/a
5	ATF1	chr15:34761374-34761389	K562	blood:	n/a	n/a
6	ATF1	chr15:34807442-34807640	K562	blood:	n/a	n/a
7	ATF1	chr15:34808283-34808324	K562	blood:	n/a	n/a
8	ATF3	chr15:34781262-34781502	K562	blood:	n/a	n/a
9	BACH1	chr15:34806578-34807213	H1-hESC	embryonic stem cell:	n/a	n/a
10	BACH1	chr15:34729369-34729390	H1-hESC	embryonic stem cell:	n/a	n/a
11	BATF	chr15:34696017-34696728	GM12878	blood:	n/a	n/a
12	BATF	chr15:34696116-34696523	GM12878	blood:	n/a	n/a
13	BATF	chr15:34762243-34762455	GM12878	blood:	n/a	n/a
14	BATF	chr15:34808073-34808311	GM12878	blood:	n/a	n/a
15	BATF	chr15:34842337-34842744	GM12878	blood:	n/a	n/a
16	BATF	chr15:34841508-34841849	GM12878	blood:	n/a	n/a
17	BATF	chr15:34842238-34842949	GM12878	blood:	n/a	n/a
18	BATF	chr15:34695287-34695628	GM12878	blood:	n/a	n/a
19	BATF	chr15:34695261-34695641	GM12878	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	BCL11A	chr15:34695333-34695638	GM12878	blood:	n/a	n/a
23	BCL11A	chr15:34816077-34816245	GM12878	blood:	n/a	chr15:34816149-34816162
24	BCL11A	chr15:34842236-34842734	GM12878	blood:	n/a	n/a
25	BCL11A	chr15:34841554-34841859	GM12878	blood:	n/a	n/a
26	BCL11A	chr15:34696015-34696513	GM12878	blood:	n/a	n/a
27	BCLAF1	chr15:34729008-34729495	GM12878	blood:	n/a	chr15:34729354-34729367 chr15:34729445-34729458
28	BCLAF1	chr15:34729841-34730371	GM12878	blood:	n/a	n/a
29	BHLHE40	chr15:34729903-34730377	HepG2	liver:	n/a	n/a
30	BHLHE40	chr15:34807389-34807610	GM12878	blood:	n/a	n/a
31	BHLHE40	chr15:34728512-34728697	K562	blood:	n/a	n/a
32	BHLHE40	chr15:34869080-34869387	K562	blood:	n/a	n/a
33	BHLHE40	chr15:34781166-34781584	K562	blood:	n/a	n/a
34	BHLHE40	chr15:34807981-34808415	GM12878	blood:	n/a	n/a
35	BHLHE40	chr15:34729879-34730508	K562	blood:	n/a	n/a
36	BHLHE40	chr15:34806536-34807767	K562	blood:	n/a	chr15:34807373-34807389 chr15:34806722-34806738
37	BHLHE40	chr15:34804947-34805071	K562	blood:	n/a	chr15:34805006-34805019 chr15:34805002-34805023
38	BHLHE40	chr15:34754120-34754185	K562	blood:	n/a	n/a
39	BHLHE40	chr15:34808048-34808404	K562	blood:	n/a	n/a
40	BHLHE40	chr15:34729075-34729345	K562	blood:	n/a	n/a
41	BHLHE40	chr15:34729886-34730498	GM12878	blood:	n/a	n/a
42	BHLHE40	chr15:34806954-34807627	HepG2	liver:	n/a	chr15:34807373-34807389
43	BHLHE40	chr15:34806518-34806718	GM12878	blood:	n/a	n/a
44	CBX3	chr15:34732091-34732455	K562	blood:	n/a	n/a
45	CBX3	chr15:34729841-34730369	K562	blood:	n/a	n/a
46	CBX3	chr15:34729889-34730257	K562	blood:	n/a	n/a
47	CBX3	chr15:34781179-34781807	K562	blood:	n/a	n/a
48	CBX3	chr15:34729907-34730280	HCT-116	colon:	n/a	n/a
49	CBX3	chr15:34807187-34807674	K562	blood:	n/a	n/a
50	CCNT2	chr15:34729140-34729519	K562	blood:	n/a	n/a

(count:1773 , 50 per page) page: 1 2 3 4 5 6 7 ... 36

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:34806349-34806399	Hela-S3	cervix:	n/a
2	chr15:34781705-34781755	NB4	blood:	n/a
3	chr15:34807679-34807729	HIPEpiC	eye:	n/a
4	chr15:34787420-34787470	AG10803	skin:	n/a
5	chr15:34806349-34806399	Hela-S3	cervix:	n/a
6	chr15:34781705-34781755	NB4	blood:	n/a
7	chr15:34807679-34807729	HIPEpiC	eye:	n/a
8	chr15:34787420-34787470	AG10803	skin:	n/a
9	chr15:34700272-34700322	U87	brain:	n/a
10	chr15:34817982-34818032	AG09319	gingival:	n/a
11	chr15:34726650-34726700	Hepatocyte	liver:	n/a
12	chr15:34812400-34812450	HPAEpiC	pulmonary alveolar:	n/a
13	chr15:34786594-34786644	A549	lung:	n/a
14	chr15:34807221-34807271	HRE	kidney:	n/a
15	chr15:34782167-34782217	RPTEC	kidney:	n/a
16	chr15:34782167-34782217	K562	blood:	n/a
17	chr15:34730071-34730121	HIPEpiC	eye:	n/a
18	chr15:34817982-34818032	NT2-D1	testis:	n/a
19	chr15:34786594-34786644	HPAEpiC	pulmonary alveolar:	n/a
20	chr15:34807221-34807271	SKMC	muscle:	n/a
21	chr15:34782820-34782870	K562	blood:	n/a
22	chr15:34786594-34786644	Jurkat	blood:	n/a
23	chr15:34729026-34729076	HPAEpiC	pulmonary alveolar:	n/a
24	chr15:34700272-34700322	MCF10A-Er-Src	breast:	n/a
25	chr15:34788847-34788897	HCF	heart:	n/a
26	chr15:34806349-34806399	AoSMC	blood vessel:	n/a
27	chr15:34781891-34781941	NT2-D1	testis:	n/a
28	chr15:34807143-34807193	HepG2	liver:	n/a
29	chr15:34729115-34729165	HUVEC	blood vessel:	n/a
30	chr15:34782167-34782217	GM12878	blood:	n/a
31	chr15:34729115-34729165	MCF10A-Er-Src	breast:	n/a
32	chr15:34787420-34787470	ProgFib	skin:	n/a
33	chr15:34812400-34812450	HCF	heart:	n/a
34	chr15:34787420-34787470	GM12892	blood:	n/a
35	chr15:34787400-34787450	GM12892	blood:	n/a
36	chr15:34807143-34807193	BJ	skin:	n/a
37	chr15:34807050-34807100	PANC-1	pancreas:	n/a
38	chr15:34817982-34818032	GM12878	blood:	n/a
39	chr15:34726650-34726700	SK-N-SH_RA	brain:	n/a
40	chr15:34729026-34729076	HMEC	breast:	n/a
41	chr15:34730071-34730121	SAEC	small airway:	n/a
42	chr15:34781891-34781941	IMR90	lung:	fetal
43	chr15:34787920-34787970	ovcar-3	ovarian:	n/a
44	chr15:34787420-34787470	HRCEpiC	kidney:	n/a
45	chr15:34788847-34788897	AG04450	lung:	fetal
46	chr15:34788017-34788067	GM06990	blood:	n/a
47	chr15:34729310-34729360	AG09309	skin:	n/a
48	chr15:34817982-34818032	SK-N-SH_RA	brain:	n/a
49	chr15:34785380-34785430	HCM	heart:	n/a
50	chr15:34806592-34806642	AG04450	lung:	fetal

(count:40 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr15:34727885..34731466-chr15:34878887..34881950,4	K562	blood:
2	chr15:34728587..34731061-chr15:34780506..34783189,3	K562	blood:
3	chr15:34759701..34761289-chr15:34761464..34762969,2	K562	blood:
4	chr15:34770080..34772217-chr15:34772786..34775252,2	K562	blood:
5	chr15:34728587..34731061-chr15:34780506..34783189,2	K562	blood:
6	chr15:34726561..34729987-chr15:34871215..34874723,3	K562	blood:
7	chr15:34770080..34772217-chr15:34772786..34775252,2	K562	blood:
8	chr15:34761476..34764376-chr15:34768521..34770931,2	K562	blood:
9	chr15:34783968..34786265-chr15:34799018..34801586,2	K562	blood:
10	chr15:34761476..34764376-chr15:34768521..34770931,2	K562	blood:
11	chr15:34728066..34730668-chr15:34791069..34792682,2	K562	blood:
12	chr15:34867657..34871070-chr15:34876144..34878325,3	K562	blood:
13	chr15:34720616..34722466-chr15:34725764..34728714,2	K562	blood:
14	chr15:34869058..34871895-chr15:34873883..34875893,3	K562	blood:
15	chr15:34786049..34786720-chr7:5632277..5632906,2	NB4	blood:
16	chr15:34729318..34730097-chr5:1799590..1800354,2	Hela-S3	cervix:
17	chr15:34774551..34776237-chr15:34779411..34782082,2	K562	blood:
18	chr15:34774551..34776237-chr15:34779411..34782082,2	K562	blood:
19	chr15:34769198..34772919-chr15:34774454..34777192,3	K562	blood:
20	chr15:34658214..34660711-chr15:34806608..34809602,2	K562	blood:
21	chr15:34762215..34765168-chr15:34878877..34880750,2	K562	blood:
22	chr15:34790342..34793794-chr15:34793900..34797346,3	K562	blood:
23	chr15:34728587..34731061-chr15:34780506..34783189,3	K562	blood:
24	chr15:34790196..34793794-chr15:34794467..34797662,3	K562	blood:
25	chr15:34728131..34733225-chr15:34735717..34740218,7	K562	blood:
26	chr15:34790196..34793794-chr15:34794467..34797662,3	K562	blood:
27	chr15:34633931..34636680-chr15:34728775..34730381,2	K562	blood:
28	chr15:34726561..34729987-chr15:34871215..34874723,3	K562	blood:
29	chr15:34727581..34729084-chr15:34874171..34876472,2	MCF-7	breast:
30	chr15:34790342..34793794-chr15:34793900..34797346,3	K562	blood:
31	chr15:34868472..34871070-chr15:34876144..34878325,2	K562	blood:
32	chr15:34728587..34731061-chr15:34780506..34783189,2	K562	blood:
33	chr15:34759701..34761289-chr15:34761464..34762969,2	K562	blood:
34	chr15:34783968..34786265-chr15:34799018..34801586,2	K562	blood:
35	chr15:34728531..34731203-chr15:34733693..34737649,5	K562	blood:
36	chr15:34769198..34772919-chr15:34774454..34777192,3	K562	blood:
37	chr15:34786054..34786721-chr7:5632299..5632821,2	HCT-116	colon:
38	chr15:34870217..34872096-chr15:35279333..35281998,2	K562	blood:
39	chr15:34727667..34729400-chr15:34875206..34876777,2	K562	blood:
40	chr15:34727095..34731466-chr15:34878887..34881950,4	K562	blood:

(count:12 , 50 per page) page: 1

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

miRNA name	Chromosome Location	mirBase accession
hsa-miR-1233-3p	chr15:34674270-34674289	MIMAT0005588
hsa-miR-1233-3p	chr15:34820491-34820510	MIMAT0005588_1
hsa-miR-1233-5p	chr15:34674327-34674348	MIMAT0022943
hsa-miR-1233-5p	chr15:34820548-34820569	MIMAT0022943_1

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

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

Variant related genes	Relation type
MIR1233-2	TF binding region
ENSG00000259892	TF binding region
GOLGA8A	TF binding region
MIR1233-1	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
MIR1233-1	CpG island
ENSG00000261081	CpG island
ENSG00000261559	CpG island
ENSG00000260639	CpG island
HNRNPLP2	CpG island
GOLGA8B	CpG island
ENSG00000075618	chromatin interactions
ENSG00000182117	chromatin interactions
ENSG00000184507	chromatin interactions
ENSG00000171421	chromatin interactions
ENSG00000176454	chromatin interactions
ENSG00000198146	chromatin interactions
ENSG00000215252	chromatin interactions
ENSG00000259917	chromatin interactions
ENSG00000175265	chromatin interactions

Extended variants
information (count: 5326 )
Associated
traits (count: 68 )

Variant overlapped rSNPs/rCNVs (count:5326 , 50 per page) page: 1 2 3 4 5 6 7 ... 107

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs546434195	chr15:34672823-34672824	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs77038074	chr15:34672835-34672836	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs142779697	chr15:34672842-34672843	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs541495431	chr15:34672852-34672853	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs535523016	chr15:34672856-34672857	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs146047009	chr15:34672896-34672897	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs556972450	chr15:34672899-34672900	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs572093224	chr15:34672913-34672914	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs139410850	chr15:34672957-34672958	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs182790630	chr15:34672977-34672978	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs531808051	chr15:34672991-34672992	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs149956153	chr15:34673008-34673009	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs562078072	chr15:34673010-34673011	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs78731837	chr15:34673058-34673059	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs149231939	chr15:34673059-34673060	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs547519364	chr15:34673072-34673073	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs3175608	chr15:34673079-34673080	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs142129811	chr15:34673085-34673086	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs3169220	chr15:34673092-34673093	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs570635538	chr15:34673095-34673096	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs188256329	chr15:34673099-34673100	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs556481648	chr15:34673117-34673118	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs574671769	chr15:34673124-34673125	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs535429793	chr15:34673128-34673129	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs16973707	chr15:34673154-34673155	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs190912077	chr15:34673161-34673162	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs182740795	chr15:34673190-34673191	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs369421183	chr15:34673231-34673232	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs1059869	chr15:34673255-34673256	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs576213831	chr15:34673264-34673265	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs543633986	chr15:34673334-34673335	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs562039062	chr15:34673341-34673342	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs529598200	chr15:34673359-34673360	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs78955581	chr15:34673376-34673377	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs187840524	chr15:34673389-34673390	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs201118538	chr15:34673401-34673402	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs555646016	chr15:34673420-34673421	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs145037938	chr15:34673448-34673449	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs192360931	chr15:34673466-34673467	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs570200845	chr15:34673524-34673525	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs575500147	chr15:34673542-34673543	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs538016723	chr15:34673546-34673547	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs550047232	chr15:34673548-34673549	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs568335392	chr15:34673554-34673555	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs535348771	chr15:34673578-34673579	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs368554203	chr15:34673588-34673589	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs199882260	chr15:34673595-34673596	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs554055734	chr15:34673621-34673622	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs371596478	chr15:34673660-34673661	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs571911651	chr15:34673676-34673677	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:68)

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

Chromatin state (count:1490 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:34660800-34674200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
2	chr15:34660800-34674400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr15:34660800-34674400	Weak transcription	Fetal Lung	lung
4	chr15:34660800-34674800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
5	chr15:34661000-34673800	Weak transcription	Duodenum Mucosa	Duodenum
6	chr15:34661000-34678000	Weak transcription	Primary T cells from cord blood	blood
7	chr15:34661200-34679600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
8	chr15:34661200-34680800	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
9	chr15:34661600-34674600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
10	chr15:34662600-34675400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
11	chr15:34662800-34723600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
12	chr15:34663000-34674800	Weak transcription	GM12878-XiMat	blood
13	chr15:34663400-34674600	Weak transcription	HSMM	muscle
14	chr15:34665400-34675200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
15	chr15:34666000-34674600	Weak transcription	Fetal Muscle Trunk	muscle
16	chr15:34666800-34674200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
17	chr15:34667200-34691600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
18	chr15:34667400-34674600	Weak transcription	Adipose Nuclei	Adipose
19	chr15:34669400-34673800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
20	chr15:34669600-34674800	Weak transcription	Brain Hippocampus Middle	brain
21	chr15:34670600-34674800	Weak transcription	Ovary	ovary
22	chr15:34670800-34674600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
23	chr15:34671200-34673600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
24	chr15:34672000-34680400	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
25	chr15:34672200-34675600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
26	chr15:34672600-34673400	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
27	chr15:34672800-34673000	Enhancers	Esophagus	oesophagus
28	chr15:34672800-34673000	Enhancers	Left Ventricle	heart
29	chr15:34672800-34673200	Strong transcription	Primary T cells fromperipheralblood	blood
30	chr15:34673000-34675200	Weak transcription	Left Ventricle	heart
31	chr15:34673200-34676200	Weak transcription	Primary T cells fromperipheralblood	blood
32	chr15:34673400-34678200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
33	chr15:34673600-34673800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
34	chr15:34685200-34686000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
35	chr15:34689600-34689800	Enhancers	Primary T cells fromperipheralblood	blood
36	chr15:34689600-34690400	Enhancers	Primary hematopoietic stem cells short term culture	blood
37	chr15:34689600-34690400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
38	chr15:34689600-34690400	Enhancers	Primary T helper cells PMA-I stimulated	--
39	chr15:34689600-34690400	Enhancers	NHEK	skin
40	chr15:34689600-34691200	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
41	chr15:34689600-34691200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
42	chr15:34689800-34690600	Weak transcription	Primary T cells fromperipheralblood	blood
43	chr15:34695200-34722600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
44	chr15:34695400-34699400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
45	chr15:34706000-34710600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
46	chr15:34706800-34724200	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
47	chr15:34707800-34710600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
48	chr15:34709000-34721800	Weak transcription	GM12878-XiMat	blood
49	chr15:34709000-34724200	Weak transcription	Fetal Stomach	stomach
50	chr15:34709200-34715400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin

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