Variant report

Variant	esv3346898
Chromosome Location	chr17:33680445-33768671
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:889)
CpG islands
(count:2385)
Chromatin interactive
region (count:10)
LncRNA
region (count:17)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:889 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr17:33760648-33760943	K562	blood:	n/a	n/a
2	ATF2	chr17:33760159-33760921	H1-hESC	embryonic stem cell:	n/a	n/a
3	ATF2	chr17:33760160-33760916	H1-hESC	embryonic stem cell:	n/a	n/a
4	ATF3	chr17:33760267-33760589	H1-hESC	embryonic stem cell:	n/a	n/a
5	ATF3	chr17:33760631-33760858	K562	blood:	n/a	n/a
6	ATF3	chr17:33760190-33760966	H1-hESC	embryonic stem cell:	n/a	n/a
7	ATF3	chr17:33760593-33760991	K562	blood:	n/a	n/a
8	ATF3	chr17:33760478-33761048	A549	lung:	n/a	n/a
9	ATF3	chr17:33760640-33760960	H1-hESC	embryonic stem cell:	n/a	n/a
10	BACH1	chr17:33759792-33760985	H1-hESC	embryonic stem cell:	n/a	chr17:33760771-33760785
11	BACH1	chr17:33700735-33700996	H1-hESC	embryonic stem cell:	n/a	n/a
12	BATF	chr17:33760594-33760881	GM12878	blood:	n/a	chr17:33760774-33760785 chr17:33760775-33760785
13	BATF	chr17:33760581-33760913	GM12878	blood:	n/a	chr17:33760774-33760785 chr17:33760775-33760785
14	BCL3	chr17:33760474-33760983	A549	lung:	n/a	chr17:33760774-33760783 chr17:33760773-33760782
15	BCLAF1	chr17:33700435-33700893	GM12878	blood:	n/a	n/a
16	BHLHE40	chr17:33700507-33700933	GM12878	blood:	n/a	n/a
17	BHLHE40	chr17:33731448-33731557	GM12878	blood:	n/a	n/a
18	BHLHE40	chr17:33765638-33765645	HepG2	liver:	n/a	n/a
19	BRCA1	chr17:33700927-33700952	Hela-S3	cervix:	n/a	n/a
20	CEBPB	chr17:33717812-33718023	K562	blood:	n/a	chr17:33717904-33717917 chr17:33717904-33717917 chr17:33717905-33717916
21	CEBPB	chr17:33717720-33718093	IMR90	lung:	n/a	chr17:33717904-33717917 chr17:33717904-33717917 chr17:33717905-33717916
22	CEBPB	chr17:33760228-33761108	A549	lung:	n/a	chr17:33761021-33761029
23	CEBPB	chr17:33701339-33701878	Hela-S3	cervix:	n/a	n/a
24	CEBPB	chr17:33731395-33731702	A549	lung:	n/a	n/a
25	CEBPB	chr17:33717739-33718092	Hela-S3	cervix:	n/a	chr17:33717904-33717917 chr17:33717904-33717917 chr17:33717905-33717916
26	CEBPB	chr17:33717723-33718092	HepG2	liver:	n/a	chr17:33717904-33717917 chr17:33717904-33717917 chr17:33717905-33717916
27	CEBPB	chr17:33760651-33760906	K562	blood:	n/a	n/a
28	CEBPB	chr17:33717673-33718118	A549	lung:	n/a	chr17:33717904-33717917 chr17:33717904-33717917 chr17:33717905-33717916
29	CEBPB	chr17:33717731-33718093	A549	lung:	n/a	chr17:33717904-33717917 chr17:33717904-33717917 chr17:33717905-33717916
30	CEBPB	chr17:33681579-33681723	IMR90	lung:	n/a	chr17:33681650-33681661
31	CEBPB	chr17:33700361-33701097	GM12878	blood:	n/a	n/a
32	CEBPB	chr17:33717730-33718103	K562	blood:	n/a	chr17:33717904-33717917 chr17:33717904-33717917 chr17:33717905-33717916
33	CEBPB	chr17:33731440-33731698	IMR90	lung:	n/a	n/a
34	CEBPB	chr17:33760241-33760955	IMR90	lung:	n/a	n/a
35	CEBPB	chr17:33698339-33698621	HepG2	liver:	n/a	chr17:33698439-33698450
36	CEBPB	chr17:33681594-33681772	HepG2	liver:	n/a	chr17:33681650-33681661
37	CEBPB	chr17:33760621-33760983	A549	lung:	n/a	n/a
38	CEBPB	chr17:33698406-33698449	H1-hESC	embryonic stem cell:	n/a	n/a
39	CEBPB	chr17:33698317-33698552	A549	lung:	n/a	chr17:33698439-33698450
40	CEBPB	chr17:33717748-33718067	H1-hESC	embryonic stem cell:	n/a	chr17:33717904-33717917 chr17:33717904-33717917 chr17:33717905-33717916
41	CEBPB	chr17:33717804-33717994	MCF-7	breast:	n/a	chr17:33717904-33717917 chr17:33717904-33717917 chr17:33717905-33717916
42	CEBPB	chr17:33731441-33731629	K562	blood:	n/a	n/a
43	CEBPB	chr17:33760660-33760956	A549	lung:	n/a	n/a
44	CEBPB	chr17:33760228-33760918	H1-hESC	embryonic stem cell:	n/a	n/a
45	CEBPB	chr17:33759330-33759655	H1-hESC	embryonic stem cell:	n/a	n/a
46	CEBPB	chr17:33731382-33731714	HepG2	liver:	n/a	n/a
47	CEBPB	chr17:33717633-33718161	A549	lung:	n/a	chr17:33717904-33717917 chr17:33717904-33717917 chr17:33717905-33717916
48	CEBPB	chr17:33701311-33701959	IMR90	lung:	n/a	n/a
49	CEBPB	chr17:33760263-33760970	Hela-S3	cervix:	n/a	n/a
50	CEBPB	chr17:33700583-33700911	Hela-S3	cervix:	n/a	n/a

(count:2385 , 50 per page) page: 1 2 3 4 5 6 7 ... 48

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr17:33700745-33700795	T-47D	breast:	n/a
2	chr17:33734664-33734714	MCF10A-Er-Src	breast:	n/a
3	chr17:33734664-33734714	Jurkat	blood:	n/a
4	chr17:33700255-33700305	SKMC	muscle:	n/a
5	chr17:33701321-33701371	GM12891	blood:	n/a
6	chr17:33700295-33700345	ovcar-3	ovarian:	n/a
7	chr17:33700745-33700795	T-47D	breast:	n/a
8	chr17:33734664-33734714	MCF10A-Er-Src	breast:	n/a
9	chr17:33734664-33734714	Jurkat	blood:	n/a
10	chr17:33700255-33700305	SKMC	muscle:	n/a
11	chr17:33701321-33701371	GM12891	blood:	n/a
12	chr17:33700295-33700345	ovcar-3	ovarian:	n/a
13	chr17:33704726-33704776	NT2-D1	testis:	n/a
14	chr17:33759512-33759562	NHDF-neo	bronchial:	n/a
15	chr17:33700230-33700280	AG09309	skin:	n/a
16	chr17:33760419-33760469	BE2_C	brain:	n/a
17	chr17:33759986-33760036	ProgFib	skin:	n/a
18	chr17:33760230-33760280	AG09319	gingival:	n/a
19	chr17:33704726-33704776	HIPEpiC	eye:	n/a
20	chr17:33759512-33759562	AG04450	lung:	fetal
21	chr17:33759986-33760036	HRPEpiC	eye:	n/a
22	chr17:33759986-33760036	NH-A	brain:	n/a
23	chr17:33760419-33760469	RPTEC	kidney:	n/a
24	chr17:33700255-33700305	HRCEpiC	kidney:	n/a
25	chr17:33698288-33698338	GM12892	blood:	n/a
26	chr17:33734481-33734531	Hela-S3	cervix:	n/a
27	chr17:33734481-33734531	Caco-2	colon:	n/a
28	chr17:33738370-33738420	MCF-7	breast:	n/a
29	chr17:33759929-33759979	GM12878	blood:	n/a
30	chr17:33738370-33738420	AG04449	skin:	fetal
31	chr17:33759929-33759979	AG04449	skin:	fetal
32	chr17:33700255-33700305	U87	brain:	n/a
33	chr17:33698288-33698338	AG09309	skin:	n/a
34	chr17:33734847-33734897	H1-hESC	embryonic stem cell:	embryo
35	chr17:33734847-33734897	HMEC	breast:	n/a
36	chr17:33700255-33700305	IMR90	lung:	fetal
37	chr17:33700747-33700797	AG09309	skin:	n/a
38	chr17:33738370-33738420	GM12892	blood:	n/a
39	chr17:33700255-33700305	HCF	heart:	n/a
40	chr17:33700757-33700807	GM19239	blood:	n/a
41	chr17:33738370-33738420	AG09319	gingival:	n/a
42	chr17:33734481-33734531	HCPEpiC	choroid plexus:	n/a
43	chr17:33738370-33738420	Hela-S3	cervix:	n/a
44	chr17:33759648-33759698	HCPEpiC	choroid plexus:	n/a
45	chr17:33698288-33698338	HRCEpiC	kidney:	n/a
46	chr17:33700255-33700305	NHBE	bronchial:	n/a
47	chr17:33734847-33734897	GM19239	blood:	n/a
48	chr17:33760230-33760280	ProgFib	skin:	n/a
49	chr17:33734847-33734897	IMR90	lung:	fetal
50	chr17:33759929-33759979	GM12891	blood:	n/a

(count:10 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr17:33760769..33763748-chr17:33765471..33767342,2	MCF-7	breast:
2	chr17:33729515..33731700-chr17:33736981..33738686,2	K562	blood:
3	chr17:33726969..33729366-chr17:33731337..33733299,2	K562	blood:
4	chr17:33749302..33751373-chr17:33754505..33756544,2	K562	blood:
5	chr17:33729515..33731700-chr17:33736981..33738686,2	K562	blood:
6	chr17:33691774..33694475-chr17:33701256..33703274,2	K562	blood:
7	chr17:33749302..33751373-chr17:33754505..33756544,2	K562	blood:
8	chr17:33676876..33678377-chr17:33681878..33683602,2	K562	blood:
9	chr17:33760769..33763748-chr17:33765471..33767342,2	MCF-7	breast:
10	chr17:33700355..33701212-chr7:100026345..100027279,2	NB4	blood:

(count:17 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SLFN12-2	chr17:33730856-33731392	ENSG00000267547.1
2	lnc-SLFN12-1	chr17:33736484-33736787	ENSG00000267745.1
3	lnc-SLFN12-6	chr17:33687038-33687390	NONHSAT053086
4	lnc-SLFN12-1	chr17:33736621-33737247	NONHSAT053094
5	lnc-SLFN12-5	chr17:33690641-33690845	NONHSAT053087
6	lnc-SLFN12-5	chr17:33693966-33694313	NONHSAT053087
7	lnc-SLFN13-1	chr17:33759207-33759276	NONHSAT053095
8	lnc-SLFN13-1	chr17:33758902-33759093	NONHSAT053095
9	lnc-SLFN12-1	chr17:33733703-33734610	ENSG00000267745.1
10	lnc-SLFN12-5	chr17:33694285-33694719	NONHSAT053088
11	lnc-SLFN12-3	chr17:33727897-33728219	ENSG00000267711.1
12	lnc-SLFN13-1	chr17:33759924-33760184	NONHSAT053095
13	lnc-SLFN11-1	chr17:33704435-33704697	NONHSAT053089
14	lnc-SLFN12-5	chr17:33700493-33700639	NONHSAT053088
15	lnc-SLFN12-3	chr17:33729955-33730025	ENSG00000267711.1
16	lnc-SLFN12-6	chr17:33689786-33690011	NONHSAT053086
17	lnc-SLFN12-1	chr17:33733967-33734837	NONHSAT053093

No data

Variant related genes	Relation type
ENSG00000267547	TF binding region
SLFN11	TF binding region
ENSG00000267648	TF binding region
ENSG00000267711	TF binding region
ENSG00000267102	TF binding region
ENSG00000267315	TF binding region
SLFN12	TF binding region
ENSG00000267745	TF binding region
ENSG00000267547	CpG island
SLFN11	CpG island
ENSG00000267648	CpG island
ENSG00000267711	CpG island
ENSG00000267102	CpG island
ENSG00000267315	CpG island
SLFN12	CpG island
ENSG00000267745	CpG island
ENSG00000078487	chromatin interactions
ENSG00000146834	chromatin interactions
ENSG00000172716	chromatin interactions
ENSG00000267711	chromatin interactions
ENSG00000267547	chromatin interactions
ENSG00000267102	chromatin interactions

Extended variants
information (count: 3296 )
Associated
traits (count: 117 )

Variant overlapped rSNPs/rCNVs (count:3296 , 50 per page) page: 1 2 3 4 5 6 7 ... 66

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs545992592	chr17:33680483-33680484	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs112159604	chr17:33680507-33680508	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs146981586	chr17:33680508-33680509	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs560527012	chr17:33680512-33680513	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs532692465	chr17:33680570-33680571	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs201829415	chr17:33680586-33680587	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs200931694	chr17:33680600-33680601	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs531866797	chr17:33680610-33680611	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs200045726	chr17:33680615-33680616	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs202115057	chr17:33680710-33680711	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs527404230	chr17:33680744-33680745	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs547424777	chr17:33680754-33680755	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs200274296	chr17:33680758-33680759	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs570453246	chr17:33680761-33680762	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs201201253	chr17:33680762-33680763	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs112950063	chr17:33680783-33680784	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs200387434	chr17:33680803-33680804	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs9897352	chr17:33680807-33680808	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs9898983	chr17:33680811-33680812	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs139588310	chr17:33680812-33680813	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs138392474	chr17:33680818-33680819	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs149238570	chr17:33680822-33680823	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs28571667	chr17:33680840-33680841	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs374964852	chr17:33680859-33680860	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs554288625	chr17:33680921-33680922	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs144863903	chr17:33680941-33680942	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs148585532	chr17:33680942-33680943	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs150001025	chr17:33680945-33680946	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs199673490	chr17:33680956-33680957	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs371752176	chr17:33680959-33680960	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs562715364	chr17:33680960-33680961	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs200730458	chr17:33680962-33680963	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs369676057	chr17:33680968-33680969	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs146126445	chr17:33680970-33680971	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs140112516	chr17:33680980-33680981	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs200531063	chr17:33680981-33680982	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs374459913	chr17:33680990-33680991	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs143719018	chr17:33681007-33681008	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs542078013	chr17:33681010-33681011	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs561531075	chr17:33681023-33681024	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs200518229	chr17:33681061-33681062	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs111294630	chr17:33681074-33681075	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs199743554	chr17:33681111-33681112	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs527330366	chr17:33681160-33681161	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs79424832	chr17:33681190-33681191	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs539978889	chr17:33681210-33681211	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs114068739	chr17:33681229-33681230	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs564242722	chr17:33681244-33681245	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs144298062	chr17:33681290-33681291	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs188147386	chr17:33681299-33681300	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:117)

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
Lung cancer	18438408	CNVD
Recurrent pregnancy loss	19789632	CNVD
Breast cancer	21364760	CNVD
small cell lung cancer	20016488	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:2096 , 50 per page) page: 1 2 3 4 5 6 7 ... 42

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr17:33673800-33689800	Weak transcription	Gastric	stomach
2	chr17:33673800-33699800	Weak transcription	Ovary	ovary
3	chr17:33674000-33681600	Weak transcription	Duodenum Mucosa	Duodenum
4	chr17:33674000-33682600	Weak transcription	NHDF-Ad	bronchial
5	chr17:33674000-33686400	Weak transcription	Rectal Mucosa Donor 31	rectum
6	chr17:33674000-33695600	Weak transcription	Colonic Mucosa	Colon
7	chr17:33674000-33695600	Weak transcription	Placenta	Placenta
8	chr17:33674000-33698600	Weak transcription	Muscle Satellite Cultured Cells	--
9	chr17:33674200-33686000	Weak transcription	Brain Hippocampus Middle	brain
10	chr17:33674200-33699800	Weak transcription	Sigmoid Colon	Sigmoid Colon
11	chr17:33674400-33693600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
12	chr17:33674600-33694600	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
13	chr17:33674800-33683600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
14	chr17:33675000-33681400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
15	chr17:33675000-33686600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
16	chr17:33675000-33688400	Weak transcription	Colon Smooth Muscle	Colon
17	chr17:33675600-33684400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
18	chr17:33675800-33687800	Strong transcription	Dnd41	blood
19	chr17:33675800-33694000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
20	chr17:33675800-33699800	Weak transcription	Rectal Smooth Muscle	rectum
21	chr17:33676000-33687600	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
22	chr17:33676000-33689600	Weak transcription	Primary neutrophils fromperipheralblood	blood
23	chr17:33676000-33689600	Weak transcription	Stomach Smooth Muscle	stomach
24	chr17:33676400-33684800	Strong transcription	Primary hematopoietic stem cells short term culture	blood
25	chr17:33677600-33681600	Weak transcription	Duodenum Smooth Muscle	Duodenum
26	chr17:33677600-33684800	Strong transcription	Monocytes-CD14+_RO01746	blood
27	chr17:33677600-33691400	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
28	chr17:33677600-33691400	Strong transcription	Primary monocytes fromperipheralblood	blood
29	chr17:33677800-33684200	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
30	chr17:33678000-33681400	Weak transcription	HUES48 Cell Line	embryonic stem cell
31	chr17:33678200-33683000	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
32	chr17:33678200-33687800	Weak transcription	Skeletal Muscle Female	skeletal muscle
33	chr17:33678400-33681400	Weak transcription	Left Ventricle	heart
34	chr17:33678400-33700000	Weak transcription	Esophagus	oesophagus
35	chr17:33678600-33682800	Strong transcription	Primary T cells fromperipheralblood	blood
36	chr17:33678600-33687400	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
37	chr17:33678800-33684800	Strong transcription	Primary B cells from peripheral blood	blood
38	chr17:33679000-33683000	Strong transcription	Spleen	Spleen
39	chr17:33679200-33681400	Weak transcription	Liver	Liver
40	chr17:33679800-33681000	Weak transcription	Rectal Mucosa Donor 29	rectum
41	chr17:33679800-33681400	Weak transcription	Osteobl	bone
42	chr17:33679800-33684400	Strong transcription	Adipose Nuclei	Adipose
43	chr17:33680000-33681400	Weak transcription	NHLF	lung
44	chr17:33680000-33681800	Weak transcription	Primary B cells from cord blood	blood
45	chr17:33680000-33687600	Weak transcription	Thymus	Thymus
46	chr17:33680000-33689400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
47	chr17:33680000-33695600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
48	chr17:33680200-33681000	Weak transcription	Primary T helper cells PMA-I stimulated	--
49	chr17:33680200-33681400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
50	chr17:33680200-33681400	Weak transcription	Lung	lung

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