Variant report

Variant	nsv574752
Chromosome Location	chr17:33731764-33760166
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr17:33760159-33760921	H1-hESC	embryonic stem cell:	n/a	n/a
2	ATF2	chr17:33760160-33760916	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr17:33759792-33760985	H1-hESC	embryonic stem cell:	n/a	chr17:33760771-33760785
4	CEBPB	chr17:33759330-33759655	H1-hESC	embryonic stem cell:	n/a	n/a
5	CHD1	chr17:33759931-33760304	H1-hESC	embryonic stem cell:	n/a	n/a
6	CHD2	chr17:33759459-33759810	GM12878	blood:	n/a	n/a
7	CTCF	chr17:33760160-33760310	HAc	cerebellar:	n/a	n/a
8	CTCF	chr17:33747700-33747910	GM12868	blood:	n/a	n/a
9	CTCF	chr17:33734653-33734762	H1-hESC	embryonic stem cell:	n/a	n/a
10	E2F4	chr17:33759495-33759712	MCF10A-Er-Src	breast:	n/a	n/a
11	E2F4	chr17:33750880-33751174	MCF10A-Er-Src	breast:	n/a	n/a
12	EBF1	chr17:33759494-33760161	GM12878	blood:	n/a	chr17:33760040-33760050 chr17:33760038-33760049
13	EBF1	chr17:33756317-33756546	GM12878	blood:	n/a	chr17:33756457-33756470
14	ELF1	chr17:33759722-33760644	GM12878	blood:	n/a	n/a
15	ELK1	chr17:33760128-33760441	GM12878	blood:	n/a	chr17:33760281-33760290 chr17:33760281-33760290
16	ELK1	chr17:33734530-33734560	GM12878	blood:	n/a	n/a
17	EP300	chr17:33759331-33759804	T-47D	breast:	n/a	n/a
18	EP300	chr17:33760124-33761012	H1-hESC	embryonic stem cell:	n/a	chr17:33760282-33760289 chr17:33760774-33760783 chr17:33760773-33760782
19	EP300	chr17:33760040-33761163	SK-N-SH	brain:	n/a	chr17:33760282-33760289 chr17:33760774-33760783 chr17:33760773-33760782
20	FOS	chr17:33759385-33759912	MCF10A-Er-Src	breast:	n/a	n/a
21	FOS	chr17:33759472-33761028	HUVEC	blood vessel:	n/a	chr17:33760392-33760404 chr17:33760774-33760782 chr17:33760772-33760784 chr17:33760393-33760403 chr17:33760772-33760783 chr17:33760773-33760782 chr17:33760394-33760402 chr17:33760773-33760783 chr17:33760774-33760783 chr17:33760395-33760406 chr17:33760774-33760781
22	FOS	chr17:33760144-33760992	MCF10A-Er-Src	breast:	n/a	chr17:33760392-33760404 chr17:33760774-33760782 chr17:33760772-33760784 chr17:33760393-33760403 chr17:33760772-33760783 chr17:33760773-33760782 chr17:33760394-33760402 chr17:33760773-33760783 chr17:33760774-33760783 chr17:33760395-33760406 chr17:33760774-33760781
23	FOS	chr17:33759474-33759860	MCF10A-Er-Src	breast:	n/a	n/a
24	FOS	chr17:33759538-33759657	MCF10A-Er-Src	breast:	n/a	n/a
25	FOS	chr17:33759502-33759795	MCF10A-Er-Src	breast:	n/a	n/a
26	FOS	chr17:33750847-33751106	MCF10A-Er-Src	breast:	n/a	n/a
27	FOS	chr17:33750862-33751171	MCF10A-Er-Src	breast:	n/a	n/a
28	FOS	chr17:33750862-33751167	MCF10A-Er-Src	breast:	n/a	n/a
29	FOS	chr17:33750866-33751107	MCF10A-Er-Src	breast:	n/a	n/a
30	FOSL1	chr17:33760152-33761118	HCT-116	colon:	n/a	chr17:33760392-33760404 chr17:33760774-33760782 chr17:33760772-33760784 chr17:33760772-33760783 chr17:33760393-33760403 chr17:33760773-33760782 chr17:33760394-33760402 chr17:33760773-33760783 chr17:33760774-33760783 chr17:33760395-33760406 chr17:33760774-33760781
31	FOSL2	chr17:33760065-33761126	SK-N-SH	brain:	n/a	chr17:33760392-33760404 chr17:33760774-33760782 chr17:33760772-33760784 chr17:33760393-33760403 chr17:33760773-33760782 chr17:33760394-33760402 chr17:33760771-33760782 chr17:33760773-33760783 chr17:33760774-33760783 chr17:33760395-33760406 chr17:33760774-33760781
32	FOXA1	chr17:33759396-33759762	T-47D	breast:	n/a	n/a
33	FOXA1	chr17:33759288-33759729	T-47D	breast:	n/a	n/a
34	GATA3	chr17:33760027-33761101	SK-N-SH	brain:	n/a	n/a
35	GTF2F1	chr17:33759440-33759876	H1-hESC	embryonic stem cell:	n/a	n/a
36	HDAC2	chr17:33760136-33760999	H1-hESC	embryonic stem cell:	n/a	chr17:33760946-33760960
37	IKZF1	chr17:33755471-33755647	GM12878	blood:	n/a	n/a
38	IRF1	chr17:33759212-33759466	K562	blood:	n/a	n/a
39	JUND	chr17:33759460-33761054	H1-hESC	embryonic stem cell:	n/a	chr17:33760392-33760404 chr17:33760774-33760782 chr17:33760772-33760784 chr17:33760393-33760403 chr17:33760773-33760782 chr17:33760394-33760402 chr17:33760773-33760783 chr17:33760774-33760783 chr17:33760395-33760406 chr17:33760774-33760781 chr17:33760772-33760783
40	JUND	chr17:33758698-33761144	SK-N-SH	brain:	n/a	chr17:33760392-33760404 chr17:33760774-33760782 chr17:33760772-33760784 chr17:33760393-33760403 chr17:33760773-33760782 chr17:33760394-33760402 chr17:33760773-33760783 chr17:33760774-33760783 chr17:33760395-33760406 chr17:33760774-33760781 chr17:33760772-33760783
41	JUND	chr17:33760027-33761125	SK-N-SH	brain:	n/a	chr17:33760392-33760404 chr17:33760774-33760782 chr17:33760772-33760784 chr17:33760393-33760403 chr17:33760773-33760782 chr17:33760394-33760402 chr17:33760773-33760783 chr17:33760774-33760783 chr17:33760395-33760406 chr17:33760774-33760781 chr17:33760772-33760783
42	JUND	chr17:33760061-33761112	SK-N-SH	brain:	n/a	chr17:33760392-33760404 chr17:33760774-33760782 chr17:33760772-33760784 chr17:33760393-33760403 chr17:33760773-33760782 chr17:33760394-33760402 chr17:33760773-33760783 chr17:33760774-33760783 chr17:33760395-33760406 chr17:33760774-33760781 chr17:33760772-33760783
43	MAFK	chr17:33741351-33741475	Hela-S3	cervix:	n/a	chr17:33741452-33741467
44	MAFK	chr17:33741329-33741622	HepG2	liver:	n/a	chr17:33741452-33741467
45	MAFK	chr17:33741354-33741611	IMR90	lung:	n/a	chr17:33741452-33741467
46	MAFK	chr17:33741334-33741588	HepG2	liver:	n/a	chr17:33741452-33741467
47	MAX	chr17:33759546-33760128	H1-hESC	embryonic stem cell:	n/a	n/a
48	MAX	chr17:33760103-33760336	GM12878	blood:	n/a	n/a
49	MAX	chr17:33760058-33761050	SK-N-SH	brain:	n/a	chr17:33760774-33760783 chr17:33760773-33760782
50	MAX	chr17:33760085-33760865	H1-hESC	embryonic stem cell:	n/a	chr17:33760774-33760783 chr17:33760773-33760782

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr17:33759929-33759979	IMR90	lung:	fetal
2	chr17:33734481-33734531	SK-N-SH	brain:	n/a
3	chr17:33734847-33734897	SAEC	small airway:	n/a
4	chr17:33734481-33734531	HCM	heart:	n/a
5	chr17:33759929-33759979	T-47D	breast:	n/a
6	chr17:33759957-33760007	HUVEC	blood vessel:	n/a
7	chr17:33759929-33759979	HMEC	breast:	n/a
8	chr17:33734481-33734531	NH-A	brain:	n/a
9	chr17:33759965-33760015	AoSMC	blood vessel:	n/a
10	chr17:33734664-33734714	MCF10A-Er-Src	breast:	n/a
11	chr17:33759573-33759623	HCT-116	colon:	n/a
12	chr17:33759573-33759623	HepG2	liver:	n/a
13	chr17:33759573-33759623	PFSK-1	brain:	n/a
14	chr17:33759929-33759979	HepG2	liver:	n/a
15	chr17:33759957-33760007	GM12878	blood:	n/a
16	chr17:33759573-33759623	HEK293	kidney:	embryo
17	chr17:33759484-33759534	AG04449	skin:	fetal
18	chr17:33759957-33760007	NT2-D1	testis:	n/a
19	chr17:33738370-33738420	ECC-1	luminal epithelium:	n/a
20	chr17:33738370-33738420	AG10803	skin:	n/a
21	chr17:33734481-33734531	U87	brain:	n/a
22	chr17:33759512-33759562	AG10803	skin:	n/a
23	chr17:33759648-33759698	IMR90	lung:	fetal
24	chr17:33734847-33734897	HCF	heart:	n/a
25	chr17:33738370-33738420	U87	brain:	n/a
26	chr17:33738370-33738420	PANC-1	pancreas:	n/a
27	chr17:33759573-33759623	AG10803	skin:	n/a
28	chr17:33759573-33759623	NH-A	brain:	n/a
29	chr17:33734481-33734531	GM12891	blood:	n/a
30	chr17:33759957-33760007	NB4	blood:	n/a
31	chr17:33759512-33759562	Jurkat	blood:	n/a
32	chr17:33759484-33759534	T-47D	breast:	n/a
33	chr17:33738370-33738420	ovcar-3	ovarian:	n/a
34	chr17:33734847-33734897	SK-N-SH	brain:	n/a
35	chr17:33759965-33760015	HRE	kidney:	n/a
36	chr17:33759986-33760036	Hela-S3	cervix:	n/a
37	chr17:33734847-33734897	GM12892	blood:	n/a
38	chr17:33734847-33734897	HCT-116	colon:	n/a
39	chr17:33759484-33759534	AG09319	gingival:	n/a
40	chr17:33759986-33760036	PANC-1	pancreas:	n/a
41	chr17:33734664-33734714	T-47D	breast:	n/a
42	chr17:33759573-33759623	HPAEpiC	pulmonary alveolar:	n/a
43	chr17:33759929-33759979	Hepatocyte	liver:	n/a
44	chr17:33734847-33734897	HepG2	liver:	n/a
45	chr17:33759965-33760015	SKMC	muscle:	n/a
46	chr17:33759648-33759698	PANC-1	pancreas:	n/a
47	chr17:33759484-33759534	Hela-S3	cervix:	n/a
48	chr17:33734664-33734714	ProgFib	skin:	n/a
49	chr17:33734481-33734531	HEEpiC	esophagus:	n/a
50	chr17:33759965-33760015	PFSK-1	brain:	n/a

No.	Distal block	Cell Line	Cell type
1	chr17:33729515..33731700-chr17:33736981..33738686,2	K562	blood:
2	chr17:33749302..33751373-chr17:33754505..33756544,2	K562	blood:
3	chr17:33749302..33751373-chr17:33754505..33756544,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SLFN12-1	chr17:33736621-33737247	NONHSAT053094
2	lnc-SLFN12-1	chr17:33733703-33734610	ENSG00000267745.1
3	lnc-SLFN12-1	chr17:33733967-33734837	NONHSAT053093
4	lnc-SLFN13-1	chr17:33758902-33759093	NONHSAT053095
5	lnc-SLFN13-1	chr17:33759924-33760184	NONHSAT053095
6	lnc-SLFN13-1	chr17:33759207-33759276	NONHSAT053095
7	lnc-SLFN12-1	chr17:33736484-33736787	ENSG00000267745.1

Variant related genes	Relation type
ENSG00000267547	TF binding region
SLFN12	TF binding region
ENSG00000267745	TF binding region
ENSG00000267648	TF binding region
ENSG00000267711	TF binding region
ENSG00000267102	TF binding region
ENSG00000267547	CpG island
SLFN12	CpG island
ENSG00000267745	CpG island
ENSG00000267648	CpG island
ENSG00000267711	CpG island
ENSG00000267102	CpG island
ENSG00000267547	chromatin interactions
ENSG00000267711	chromatin interactions

Extended variants
information (count: 1136 )
Associated
traits (count: 115 )

Variant overlapped rSNPs/rCNVs (count:1136 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2671828	chr17:33731764-33731765	Weak transcription Enhancers	TF binding region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs547375952	chr17:33731782-33731783	Weak transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
3	rs570369616	chr17:33731801-33731802	Weak transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
4	rs12937141	chr17:33731895-33731896	Weak transcription Enhancers	TF binding region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs68145461	chr17:33731931-33731932	Weak transcription Enhancers	TF binding region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
6	rs368499286	chr17:33731979-33731980	Weak transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
7	rs146468647	chr17:33732000-33732001	Weak transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
8	rs193126302	chr17:33732009-33732010	Weak transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
9	rs375826531	chr17:33732049-33732050	Weak transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
10	rs568853594	chr17:33732105-33732106	Weak transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
11	rs555020889	chr17:33732139-33732140	Weak transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
12	rs574939184	chr17:33732144-33732145	Weak transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
13	rs184841888	chr17:33732158-33732159	Weak transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
14	rs560659929	chr17:33732170-33732171	Weak transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
15	rs533087831	chr17:33732174-33732175	Weak transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
16	rs139133635	chr17:33732186-33732187	Weak transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
17	rs187554637	chr17:33732237-33732238	Weak transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
18	rs192032506	chr17:33732284-33732285	Weak transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
19	rs531300064	chr17:33732310-33732311	Weak transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
20	rs2671827	chr17:33732330-33732331	Weak transcription Enhancers	TF binding region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
21	rs143159931	chr17:33732366-33732367	Weak transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
22	rs147452321	chr17:33732370-33732371	Weak transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
23	rs547607573	chr17:33732417-33732418	Weak transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
24	rs576401187	chr17:33732484-33732485	Weak transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
25	rs148096743	chr17:33732488-33732489	Weak transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
26	rs141982341	chr17:33732502-33732503	Weak transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
27	rs150698579	chr17:33732514-33732515	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs568925049	chr17:33732526-33732527	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs35588365	chr17:33732548-33732549	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs184187076	chr17:33732567-33732568	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs200476217	chr17:33732577-33732578	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs574917964	chr17:33732581-33732582	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs66646145	chr17:33732582-33732583	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
34	rs369811080	chr17:33732593-33732594	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs79930506	chr17:33732600-33732601	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs577499952	chr17:33732658-33732659	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs546537832	chr17:33732692-33732693	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs139834358	chr17:33732693-33732694	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs35896700	chr17:33732730-33732731	Weak transcription Strong transcription	TF binding region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs376051735	chr17:33732746-33732747	Weak transcription Strong transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
41	rs541765824	chr17:33732752-33732753	Weak transcription Strong transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
42	rs143809238	chr17:33732799-33732800	Weak transcription Strong transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
43	rs527427253	chr17:33732817-33732818	Weak transcription Strong transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
44	rs146378239	chr17:33732893-33732894	Weak transcription Strong transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
45	rs563973561	chr17:33732895-33732896	Weak transcription Strong transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
46	rs17548645	chr17:33732932-33732933	Weak transcription Strong transcription	TF binding region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
47	rs549669244	chr17:33732933-33732934	Weak transcription Strong transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
48	rs2681074	chr17:33732944-33732945	Weak transcription Strong transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
49	rs545790794	chr17:33732962-33732963	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs529165165	chr17:33732998-33732999	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:115)

Disease	PMID	Source
Melanoma	18172304	CNVD
Wilms tumour	21544195	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Ewing''s sarcoma	21437220	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
Ovarian cancer	22174824	CNVD
Moyamoya disease	22323933	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Cancer	20164919	CNVD
Ovarian cancer	21781307	CNVD
Colorectal cancer	21645411	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Medulloblastoma	21979893	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Hodgkin''s lymphoma	17606441	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute myeloid leukemia	20729466	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Breast cancer	17603634	CNVD
T-cell lymphomas	19863542	CNVD
Cancer	16751803	CNVD
Chordoma	21602918	CNVD
Neurofibromatosis	20686819	CNVD
Peripheral nerve sheath tumors	20686819	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Cancer	21499728	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Medulloblastoma	21292688	CNVD
Neuroblastoma	18923524	CNVD
Neuroblastoma	17897457	CNVD
Neuroblastoma	17327916	CNVD
Breast cancer	21264507	CNVD
Endometrial cancer	22040021	CNVD
Neuroblastoma	21484798	CNVD
Breast cancer	22028636	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute myeloid leukemia	20724749	CNVD
Breast cancer	21858162	CNVD
Breast cancer	16397240	CNVD
Myxofibrosarcoma	16751306	CNVD
lymphocytic leukemia	21291569	CNVD
Breast cancer	17001317	CNVD
Breast cancer	17157792	CNVD
Bladder cancer	19088036	CNVD
Gastric cancer	17167181	CNVD
Breast cancer	19287154	CNVD
Leukemia	20874852	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Neuroblastoma	18664255	CNVD
Neuroblastoma	17533364	CNVD
Human rectal carcinomas	16397240	CNVD
Meningioma	19431122	CNVD
Neurocytoma	17123091	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Lung cancer	21911935	CNVD
Breast cancer	22048815	CNVD
Cervical cancer	21062161	CNVD
Colorectal cancer	22860045	CNVD
Ductal carcinoma	18381933	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	16417655	CNVD
Renal cysts	20603712	CNVD
Epilepsy	21858020	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
Autism	20587423	CNVD
Renal cysts	20587423	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Cancer	21183584	CNVD
Ovarian cancer	20844748	CNVD
Mayer-Rokitansky-Kuster-Hauser syndrome	19889212	CNVD
Endometrial cancer	23636398	CNVD
Urothelial cell carcinoma	18451213	CNVD
Gastric cancer	24379144	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	16608533	CNVD
Gastric cancer	18160780	CNVD
Hepatocellular carcinoma	16785998	CNVD
Breast cancer	17850661	CNVD
Primary lung adenocarcinoma	16799635	CNVD
HIV/AIDS	18848619	CNVD
Rheumatoid arthritis	19220326	CNVD
Rheumatoid arthritis	18848619	CNVD
Systemic lupus erythematosus	19220326	CNVD
Systemic lupus erythematosus	18848619	CNVD
Type 1 diabetes	19220326	CNVD
HIV/AIDS	17330138	CNVD
Basal cell lymphoma	17053054	CNVD
Autism	19955444	CNVD
Schizophrenia	19955444	CNVD
Acute monocytic leukemia	16498392	CNVD
Breast cancer	20409316	CNVD
Myelodysplastic syndrome	18663149	CNVD
Breast cancer	17457667	CNVD
Breast cancer	16951389	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Lung cancer	19153074	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	21785460	CNVD
Breast cancer	20932292	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Breast cancer	21364760	CNVD
small cell lung cancer	20016488	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Lung cancer	18438408	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:932 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr17:33717200-33732600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
2	chr17:33721200-33733800	Weak transcription	Monocytes-CD14+_RO01746	blood
3	chr17:33721400-33732800	Weak transcription	Primary monocytes fromperipheralblood	blood
4	chr17:33725400-33734400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr17:33727400-33734000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
6	chr17:33727600-33734000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
7	chr17:33727600-33736800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
8	chr17:33728200-33734200	Weak transcription	HSMM	muscle
9	chr17:33728600-33733600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
10	chr17:33729800-33734000	Weak transcription	HUVEC	blood vessel
11	chr17:33730000-33733800	Weak transcription	NHLF	lung
12	chr17:33730000-33734400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
13	chr17:33730000-33736200	Weak transcription	Fetal Kidney	kidney
14	chr17:33730200-33733800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
15	chr17:33730200-33736800	Weak transcription	HUES48 Cell Line	embryonic stem cell
16	chr17:33730800-33733400	Weak transcription	HUES6 Cell Line	embryonic stem cell
17	chr17:33731000-33732600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
18	chr17:33731000-33733800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
19	chr17:33731000-33734000	Weak transcription	Sigmoid Colon	Sigmoid Colon
20	chr17:33731000-33734200	Weak transcription	Fetal Muscle Trunk	muscle
21	chr17:33731000-33734400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
22	chr17:33731200-33731800	Enhancers	Primary T killer memory cells from peripheral blood	blood
23	chr17:33731200-33732000	Enhancers	Primary T killer naive cells fromperipheralblood	blood
24	chr17:33731200-33733800	Weak transcription	Fetal Lung	lung
25	chr17:33731200-33734000	Weak transcription	Placenta	Placenta
26	chr17:33731200-33734000	Weak transcription	Left Ventricle	heart
27	chr17:33731200-33736800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
28	chr17:33731400-33731800	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
29	chr17:33731400-33731800	Enhancers	Primary T helper naive cells from peripheral blood	blood
30	chr17:33731400-33731800	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
31	chr17:33731400-33732600	Enhancers	Dnd41	blood
32	chr17:33731400-33735800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
33	chr17:33731400-33736400	Weak transcription	Duodenum Mucosa	Duodenum
34	chr17:33731400-33736800	Weak transcription	Rectal Mucosa Donor 31	rectum
35	chr17:33731400-33754800	Weak transcription	Primary T helper cells PMA-I stimulated	--
36	chr17:33731600-33731800	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
37	chr17:33731600-33731800	Enhancers	Primary T helper cells fromperipheralblood	blood
38	chr17:33731800-33734600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
39	chr17:33731800-33735800	Weak transcription	HUES64 Cell Line	embryonic stem cell
40	chr17:33731800-33736800	Weak transcription	Primary T helper cells fromperipheralblood	blood
41	chr17:33731800-33754600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
42	chr17:33731800-33755200	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
43	chr17:33732000-33733600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
44	chr17:33732000-33734000	Weak transcription	Fetal Muscle Leg	muscle
45	chr17:33732000-33736800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
46	chr17:33732000-33736800	Weak transcription	NHDF-Ad	bronchial
47	chr17:33732000-33737000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
48	chr17:33732000-33737600	Weak transcription	Muscle Satellite Cultured Cells	--
49	chr17:33732200-33733800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
50	chr17:33732200-33733800	Weak transcription	NH-A	brain

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