Variant report

Variant	nsv568917
Chromosome Location	chr15:33167171-33304172
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1567)
CpG islands
(count:1040)
Chromatin interactive
region (count:50)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1567 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr15:33287094-33287423	K562	blood:	n/a	n/a
2	ATF1	chr15:33172177-33172299	K562	blood:	n/a	n/a
3	ATF1	chr15:33218767-33218893	K562	blood:	n/a	n/a
4	ATF2	chr15:33191373-33191925	H1-hESC	embryonic stem cell:	n/a	n/a
5	ATF2	chr15:33191348-33191883	H1-hESC	embryonic stem cell:	n/a	n/a
6	ATF2	chr15:33200491-33201087	GM12878	blood:	n/a	n/a
7	BACH1	chr15:33175656-33175900	H1-hESC	embryonic stem cell:	n/a	n/a
8	BACH1	chr15:33221160-33221387	H1-hESC	embryonic stem cell:	n/a	n/a
9	BACH1	chr15:33248180-33248533	H1-hESC	embryonic stem cell:	n/a	n/a
10	BACH1	chr15:33173812-33174063	H1-hESC	embryonic stem cell:	n/a	n/a
11	BACH1	chr15:33175154-33175210	H1-hESC	embryonic stem cell:	n/a	n/a
12	BATF	chr15:33216573-33216893	GM12878	blood:	n/a	n/a
13	BATF	chr15:33216580-33216867	GM12878	blood:	n/a	n/a
14	BATF	chr15:33200675-33201039	GM12878	blood:	n/a	n/a
15	BCL11A	chr15:33216557-33216912	GM12878	blood:	n/a	n/a
16	BCL11A	chr15:33200755-33201026	GM12878	blood:	n/a	chr15:33200826-33200835
17	BCL11A	chr15:33200637-33201056	GM12878	blood:	n/a	chr15:33200826-33200835
18	BCL11A	chr15:33191394-33191852	H1-hESC	embryonic stem cell:	n/a	chr15:33191642-33191655
19	BCL11A	chr15:33191354-33191789	H1-hESC	embryonic stem cell:	n/a	chr15:33191642-33191655
20	BCLAF1	chr15:33200479-33201139	GM12878	blood:	n/a	chr15:33200826-33200835
21	BCLAF1	chr15:33216507-33216804	GM12878	blood:	n/a	n/a
22	BHLHE40	chr15:33200447-33201288	GM12878	blood:	n/a	n/a
23	BHLHE40	chr15:33191303-33191733	GM12878	blood:	n/a	n/a
24	BHLHE40	chr15:33216326-33216884	GM12878	blood:	n/a	n/a
25	BHLHE40	chr15:33297971-33297975	GM12878	blood:	n/a	n/a
26	BHLHE40	chr15:33247941-33248082	K562	blood:	n/a	n/a
27	CEBPB	chr15:33280725-33280887	HepG2	liver:	n/a	chr15:33280786-33280797
28	CEBPB	chr15:33219348-33219678	K562	blood:	n/a	chr15:33219513-33219524
29	CEBPB	chr15:33219343-33219706	A549	lung:	n/a	chr15:33219513-33219524
30	CEBPB	chr15:33246407-33246724	IMR90	lung:	n/a	chr15:33246558-33246569 chr15:33246558-33246571 chr15:33246558-33246571
31	CEBPB	chr15:33219349-33219704	IMR90	lung:	n/a	chr15:33219513-33219524
32	CEBPB	chr15:33221400-33221585	A549	lung:	n/a	n/a
33	CEBPB	chr15:33246445-33246700	HepG2	liver:	n/a	chr15:33246558-33246569 chr15:33246558-33246571 chr15:33246558-33246571
34	CEBPB	chr15:33242331-33242577	IMR90	lung:	n/a	n/a
35	CEBPB	chr15:33197305-33197615	HepG2	liver:	n/a	chr15:33197414-33197427 chr15:33197414-33197427
36	CEBPB	chr15:33276846-33277157	IMR90	lung:	n/a	chr15:33277005-33277016
37	CEBPB	chr15:33266920-33267199	A549	lung:	n/a	chr15:33267062-33267073 chr15:33267033-33267045
38	CEBPB	chr15:33266880-33267254	IMR90	lung:	n/a	chr15:33267062-33267073 chr15:33267033-33267045
39	CEBPB	chr15:33194527-33194734	IMR90	lung:	n/a	chr15:33194585-33194596 chr15:33194585-33194598 chr15:33194585-33194598 chr15:33194585-33194596
40	CEBPB	chr15:33195815-33196158	HepG2	liver:	n/a	n/a
41	CEBPB	chr15:33266895-33267256	ECC-1	luminal epithelium:	n/a	chr15:33267062-33267073 chr15:33267033-33267045
42	CEBPB	chr15:33258823-33259097	Hela-S3	cervix:	n/a	chr15:33258951-33258964 chr15:33258952-33258963
43	CEBPB	chr15:33195841-33196135	K562	blood:	n/a	n/a
44	CEBPB	chr15:33258909-33259085	H1-hESC	embryonic stem cell:	n/a	chr15:33258951-33258964 chr15:33258952-33258963
45	CEBPB	chr15:33195807-33196154	IMR90	lung:	n/a	n/a
46	CEBPB	chr15:33219345-33219673	H1-hESC	embryonic stem cell:	n/a	chr15:33219513-33219524
47	CEBPB	chr15:33236366-33236651	K562	blood:	n/a	chr15:33236518-33236531 chr15:33236518-33236529 chr15:33236518-33236531 chr15:33236637-33236649 chr15:33236519-33236530
48	CEBPB	chr15:33242858-33243087	A549	lung:	n/a	n/a
49	CEBPB	chr15:33210029-33210280	K562	blood:	n/a	chr15:33210196-33210209 chr15:33210196-33210207
50	CEBPB	chr15:33195831-33196118	A549	lung:	n/a	n/a

(count:1040 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:33177867-33177917	RPTEC	kidney:	n/a
2	chr15:33266926-33266976	PANC-1	pancreas:	n/a
3	chr15:33179514-33179564	SK-N-MC	brain:	n/a
4	chr15:33177867-33177917	RPTEC	kidney:	n/a
5	chr15:33266926-33266976	PANC-1	pancreas:	n/a
6	chr15:33179514-33179564	SK-N-MC	brain:	n/a
7	chr15:33278159-33278209	HPAEpiC	pulmonary alveolar:	n/a
8	chr15:33177867-33177917	Caco-2	colon:	n/a
9	chr15:33191698-33191748	HepG2	liver:	n/a
10	chr15:33220732-33220782	Hepatocyte	liver:	n/a
11	chr15:33259575-33259625	RPTEC	kidney:	n/a
12	chr15:33251279-33251329	LNCaP	prostate:	n/a
13	chr15:33259575-33259625	IMR90	lung:	fetal
14	chr15:33179514-33179564	Jurkat	blood:	n/a
15	chr15:33200866-33200916	SKMC	muscle:	n/a
16	chr15:33278159-33278209	HCPEpiC	choroid plexus:	n/a
17	chr15:33259575-33259625	SK-N-SH_RA	brain:	n/a
18	chr15:33245281-33245331	HRPEpiC	eye:	n/a
19	chr15:33177867-33177917	SK-N-SH	brain:	n/a
20	chr15:33188759-33188809	HRCEpiC	kidney:	n/a
21	chr15:33171339-33171389	NT2-D1	testis:	n/a
22	chr15:33266926-33266976	SK-N-SH	brain:	n/a
23	chr15:33178652-33178702	PrEC	prostate:	n/a
24	chr15:33220732-33220782	HEEpiC	esophagus:	n/a
25	chr15:33188759-33188809	SK-N-SH_RA	brain:	n/a
26	chr15:33188759-33188809	SAEC	small airway:	n/a
27	chr15:33195247-33195297	HPAEpiC	pulmonary alveolar:	n/a
28	chr15:33235802-33235852	ProgFib	skin:	n/a
29	chr15:33191698-33191748	Hepatocyte	liver:	n/a
30	chr15:33220732-33220782	HMEC	breast:	n/a
31	chr15:33178652-33178702	H1-hESC	embryonic stem cell:	embryo
32	chr15:33191698-33191748	HCM	heart:	n/a
33	chr15:33300472-33300522	GM12891	blood:	n/a
34	chr15:33171339-33171389	SK-N-SH	brain:	n/a
35	chr15:33188759-33188809	RPTEC	kidney:	n/a
36	chr15:33235802-33235852	A549	lung:	n/a
37	chr15:33220732-33220782	GM06990	blood:	n/a
38	chr15:33245281-33245331	SK-N-MC	brain:	n/a
39	chr15:33191698-33191748	NB4	blood:	n/a
40	chr15:33300472-33300522	HIPEpiC	eye:	n/a
41	chr15:33278159-33278209	ovcar-3	ovarian:	n/a
42	chr15:33211107-33211157	HEK293	kidney:	embryo
43	chr15:33251279-33251329	K562	blood:	n/a
44	chr15:33220732-33220782	GM19239	blood:	n/a
45	chr15:33191698-33191748	PFSK-1	brain:	n/a
46	chr15:33195247-33195297	HEK293	kidney:	embryo
47	chr15:33300472-33300522	HRE	kidney:	n/a
48	chr15:33259575-33259625	GM12878	blood:	n/a
49	chr15:33266926-33266976	A549	lung:	n/a
50	chr15:33300472-33300522	Caco-2	colon:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr15:33300871..33303669-chr15:33360060..33362322,2	MCF-7	breast:
2	chr15:33244172..33246376-chr15:33247943..33250082,2	K562	blood:
3	chr15:32943540..32944373-chr15:33286720..33287432,3	MCF-7	breast:
4	chr15:32954517..32955503-chr15:33228158..33229122,2	MCF-7	breast:
5	chr15:33136574..33137426-chr15:33228228..33228738,2	K562	blood:
6	chr15:33301497..33303169-chr15:33347240..33349716,2	MCF-7	breast:
7	chr15:33298305..33300128-chr15:33304629..33307307,2	MCF-7	breast:
8	chr15:33264165..33266280-chr15:33277864..33279978,2	MCF-7	breast:
9	chr15:32954530..32955477-chr15:33288087..33289002,2	K562	blood:
10	chr15:33244808..33246374-chr15:33249318..33251534,2	MCF-7	breast:
11	chr15:33299875..33302830-chr15:33303027..33306565,4	MCF-7	breast:
12	chr15:33244172..33246376-chr15:33247943..33250082,2	K562	blood:
13	chr15:33244592..33247228-chr15:33248722..33251718,2	MCF-7	breast:
14	chr15:33276577..33278445-chr15:33292733..33295082,2	MCF-7	breast:
15	chr15:33244592..33247228-chr15:33248722..33251718,2	MCF-7	breast:
16	chr15:33177002..33179276-chr15:33196689..33199398,2	K562	blood:
17	chr15:33194367..33197072-chr15:33201375..33203984,2	MCF-7	breast:
18	chr15:33264165..33266280-chr15:33277864..33279978,2	MCF-7	breast:
19	chr15:33264185..33265845-chr15:33271129..33273337,2	MCF-7	breast:
20	chr15:33191578..33193662-chr15:33205151..33207936,2	MCF-7	breast:
21	chr15:33177002..33179276-chr15:33196689..33199398,2	K562	blood:
22	chr15:32954026..32955488-chr15:33286759..33287801,5	K562	blood:
23	chr15:33136039..33136889-chr15:33228248..33228998,3	MCF-7	breast:
24	chr15:33269846..33272331-chr15:33277220..33279147,3	K562	blood:
25	chr15:33203701..33205590-chr15:33205602..33207495,2	MCF-7	breast:
26	chr15:33269846..33272331-chr15:33277220..33279147,3	K562	blood:
27	chr15:33264185..33265845-chr15:33271129..33273337,2	MCF-7	breast:
28	chr15:32954901..32955435-chr15:33286799..33287653,2	MCF-7	breast:
29	chr15:33287991..33290554-chr15:33293399..33295008,2	K562	blood:
30	chr15:33289408..33292508-chr15:33359912..33362781,5	MCF-7	breast:
31	chr15:33276577..33278445-chr15:33292733..33295082,2	MCF-7	breast:
32	chr15:33232993..33235695-chr15:33238081..33239940,2	K562	blood:
33	chr15:33194367..33197072-chr15:33201375..33203984,2	MCF-7	breast:
34	chr15:33136011..33136698-chr15:33286980..33287655,2	K562	blood:
35	chr15:33297830..33309224-chr15:33355310..33362883,25	MCF-7	breast:
36	chr15:33245362..33248334-chr15:33358852..33360940,3	MCF-7	breast:
37	chr15:33237429..33239397-chr15:33241975..33243636,2	MCF-7	breast:
38	chr15:33191297..33193263-chr15:33193347..33195988,2	K562	blood:
39	chr15:32954601..32955459-chr15:33247920..33248524,2	MCF-7	breast:
40	chr15:33203701..33205590-chr15:33205602..33207495,2	MCF-7	breast:
41	chr15:33299011..33299669-chr15:33424327..33425140,2	MCF-7	breast:
42	chr15:33244808..33246374-chr15:33249318..33251534,2	MCF-7	breast:
43	chr15:32931325..32933308-chr15:33284072..33286426,2	K562	blood:
44	chr15:32941628..32942202-chr15:33286760..33287625,2	MCF-7	breast:
45	chr15:33237429..33239397-chr15:33241975..33243636,2	MCF-7	breast:
46	chr15:33232993..33235695-chr15:33238081..33239940,2	K562	blood:
47	chr15:33287991..33290554-chr15:33293399..33295008,2	K562	blood:
48	chr15:33159839..33162457-chr15:33167259..33169460,2	K562	blood:
49	chr15:33191578..33193662-chr15:33205151..33207936,2	MCF-7	breast:
50	chr15:33298321..33300066-chr15:33361018..33362893,2	MCF-7	breast:

No data

Variant related genes	Relation type
HNRNPA1P71	TF binding region
ENSG00000212415	TF binding region
FMN1	TF binding region
ENSG00000238342	TF binding region
HNRNPA1P71	CpG island
ENSG00000212415	CpG island
FMN1	CpG island
ENSG00000238342	CpG island
ENSG00000259686	chromatin interactions
ENSG00000248905	chromatin interactions

Extended variants
information (count: 6814 )
Associated
traits (count: 90 )

Variant overlapped rSNPs/rCNVs (count:6814 , 50 per page) page: 1 2 3 4 5 6 7 ... 137

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs12595789	chr15:33167171-33167172	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs571464769	chr15:33167208-33167209	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs532343470	chr15:33167219-33167220	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs386782738	chr15:33167229-33167230	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs143688853	chr15:33167230-33167231	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs536385730	chr15:33167282-33167283	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs554859541	chr15:33167329-33167330	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs567080555	chr15:33167343-33167344	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs181691173	chr15:33167360-33167361	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs534212320	chr15:33167392-33167393	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs559172218	chr15:33167433-33167434	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs577636081	chr15:33167453-33167454	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs544976443	chr15:33167454-33167455	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs187155644	chr15:33167489-33167490	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs189388053	chr15:33167490-33167491	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs62001318	chr15:33167503-33167504	Weak transcription Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs1451891	chr15:33167511-33167512	Weak transcription Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs1451890	chr15:33167529-33167530	Weak transcription Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
19	rs540077153	chr15:33167573-33167574	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs542865543	chr15:33167598-33167599	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs572919412	chr15:33167650-33167651	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs565139928	chr15:33167660-33167661	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs532281856	chr15:33167663-33167664	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs151064434	chr15:33167686-33167687	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs142328841	chr15:33167799-33167800	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs376411944	chr15:33167804-33167805	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs146401958	chr15:33167814-33167815	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs79626564	chr15:33167817-33167818	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs1562933	chr15:33167830-33167831	Enhancers Weak transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs117885069	chr15:33167861-33167862	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs77121487	chr15:33167863-33167864	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs181408244	chr15:33167886-33167887	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs185176479	chr15:33167914-33167915	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs1562932	chr15:33167931-33167932	Enhancers Weak transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs538579662	chr15:33168000-33168001	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs556993757	chr15:33168019-33168020	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs1562931	chr15:33168034-33168035	Weak transcription Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs1562930	chr15:33168043-33168044	Weak transcription Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
39	rs554619887	chr15:33168065-33168066	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs1562929	chr15:33168075-33168076	Weak transcription Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs75069164	chr15:33168082-33168083	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs75007698	chr15:33168085-33168086	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs576720184	chr15:33168127-33168128	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs116174059	chr15:33168132-33168133	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs1562928	chr15:33168140-33168141	Weak transcription Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs530004216	chr15:33168153-33168154	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs370831782	chr15:33168159-33168160	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs548315383	chr15:33168180-33168181	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs560590003	chr15:33168187-33168188	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs527794131	chr15:33168215-33168216	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:90)

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
Autism	17322880	CNVD
Prader-willi syndrome	19329560	CNVD
Autism	17999366	CNVD
Autism	17901113	CNVD
Neurodevelopmental disorder	17015230	CNVD
Autism	18414403	CNVD
Neurocytoma	17123091	CNVD
Mental retardation	18923513	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
Breast cancer	21509527	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
Autism	19521722	CNVD
Bipolar disorder	19114987	CNVD
Epilepsy	19521722	CNVD
Mental retardation	19521722	CNVD
Schizophrenia	19521646	CNVD
Autism	19050728	CNVD
Schizophrenia	19348701	CNVD
Schizophrenia	18668039	CNVD
Schizophrenia	18990708	CNVD
Schizophrenia	19571808	CNVD
Velocardiofacial syndrome	19329560	CNVD
Schizophrenia	19443537	CNVD
Epilepsy	20923578	CNVD
Autism	19955444	CNVD
Autism	20964600	CNVD
Schizophrenia	19955444	CNVD
Olfactory neuroblastoma	18408657	CNVD
Legius syndrome	19443465	CNVD
Holoprosencephaly	21359414	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	22286061	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:1482 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:33138800-33190600	Weak transcription	Thymus	Thymus
2	chr15:33139600-33190600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
3	chr15:33142600-33168200	Genic enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
4	chr15:33147000-33191400	Weak transcription	Lung	lung
5	chr15:33149000-33202000	Weak transcription	Primary T helper cells fromperipheralblood	blood
6	chr15:33149600-33169600	Weak transcription	Placenta Amnion	Placenta Amnion
7	chr15:33153800-33173200	Weak transcription	Primary T helper cells PMA-I stimulated	--
8	chr15:33154400-33173800	Weak transcription	Placenta	Placenta
9	chr15:33154400-33192800	Weak transcription	Colonic Mucosa	Colon
10	chr15:33154400-33216800	Weak transcription	Fetal Thymus	thymus
11	chr15:33155000-33208200	Weak transcription	Fetal Kidney	kidney
12	chr15:33159800-33169400	Weak transcription	HUVEC	blood vessel
13	chr15:33160000-33201800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
14	chr15:33162000-33168200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
15	chr15:33162000-33178400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
16	chr15:33162200-33176400	Weak transcription	Rectal Mucosa Donor 29	rectum
17	chr15:33162200-33202400	Weak transcription	Gastric	stomach
18	chr15:33163400-33169600	Weak transcription	NH-A	brain
19	chr15:33163400-33174400	Weak transcription	Rectal Mucosa Donor 31	rectum
20	chr15:33163800-33167400	Enhancers	Fetal Stomach	stomach
21	chr15:33164000-33168600	Enhancers	Pancreatic Islets	Pancreatic Islet
22	chr15:33164400-33167400	Enhancers	Colon Smooth Muscle	Colon
23	chr15:33165000-33171600	Weak transcription	Aorta	Aorta
24	chr15:33165400-33170600	Weak transcription	Duodenum Smooth Muscle	Duodenum
25	chr15:33165600-33169000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
26	chr15:33165600-33178600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
27	chr15:33165800-33170200	Weak transcription	Rectal Smooth Muscle	rectum
28	chr15:33165800-33171600	Weak transcription	Adipose Nuclei	Adipose
29	chr15:33166000-33167200	Enhancers	Stomach Smooth Muscle	stomach
30	chr15:33166000-33169800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
31	chr15:33166000-33170000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
32	chr15:33166000-33170200	Weak transcription	NHLF	lung
33	chr15:33166000-33170400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
34	chr15:33166000-33170400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
35	chr15:33166000-33170400	Weak transcription	Sigmoid Colon	Sigmoid Colon
36	chr15:33166000-33170800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
37	chr15:33166000-33175400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
38	chr15:33166000-33202400	Weak transcription	Pancreas	Pancrea
39	chr15:33166200-33169600	Weak transcription	NHDF-Ad	bronchial
40	chr15:33166200-33169600	Weak transcription	Osteobl	bone
41	chr15:33166200-33169800	Weak transcription	HSMM	muscle
42	chr15:33166200-33211800	Weak transcription	HSMMtube	muscle
43	chr15:33166600-33167400	Enhancers	Liver	Liver
44	chr15:33166600-33167400	Strong transcription	Monocytes-CD14+_RO01746	blood
45	chr15:33166600-33167600	Enhancers	Stomach Mucosa	stomach
46	chr15:33166800-33167200	Enhancers	HepG2	liver
47	chr15:33166800-33169600	Weak transcription	Muscle Satellite Cultured Cells	--
48	chr15:33167000-33167400	Enhancers	A549	lung
49	chr15:33167200-33170000	Weak transcription	Stomach Smooth Muscle	stomach
50	chr15:33167400-33170400	Weak transcription	Colon Smooth Muscle	Colon

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