Variant report

Variant	esv3325187
Chromosome Location	chr17:38374651-38377199
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	ARID3A	chr17:38375292-38375569	HepG2	liver:	n/a	n/a
2	ARID3A	chr17:38375208-38375525	K562	blood:	n/a	n/a
3	ATF1	chr17:38374865-38375602	K562	blood:	n/a	n/a
4	ATF2	chr17:38374809-38375561	H1-hESC	embryonic stem cell:	n/a	n/a
5	ATF2	chr17:38374783-38375257	H1-hESC	embryonic stem cell:	n/a	n/a
6	ATF2	chr17:38374806-38375488	GM12878	blood:	n/a	n/a
7	ATF2	chr17:38374777-38375615	GM12878	blood:	n/a	n/a
8	ATF3	chr17:38374577-38375131	A549	lung:	n/a	chr17:38375030-38375040 chr17:38375032-38375043 chr17:38375032-38375040
9	ATF3	chr17:38374940-38375474	A549	lung:	n/a	chr17:38375030-38375040 chr17:38375032-38375043 chr17:38375032-38375040
10	BACH1	chr17:38374960-38376161	H1-hESC	embryonic stem cell:	n/a	n/a
11	BCL3	chr17:38375859-38376525	A549	lung:	n/a	chr17:38375908-38375917
12	BCL3	chr17:38375062-38375602	A549	lung:	n/a	n/a
13	BCL3	chr17:38374984-38375604	A549	lung:	n/a	n/a
14	BHLHE40	chr17:38375000-38375609	K562	blood:	n/a	n/a
15	BRCA1	chr17:38375349-38375549	HepG2	liver:	n/a	n/a
16	BRCA1	chr17:38375100-38375128	HepG2	liver:	n/a	n/a
17	CBX3	chr17:38375926-38376261	K562	blood:	n/a	n/a
18	CBX3	chr17:38374988-38375697	K562	blood:	n/a	n/a
19	CCNT2	chr17:38375510-38375658	K562	blood:	n/a	n/a
20	CEBPB	chr17:38374978-38375216	K562	blood:	n/a	n/a
21	CEBPD	chr17:38375272-38376242	HepG2	liver:	n/a	n/a
22	CHD2	chr17:38375296-38375526	HepG2	liver:	n/a	n/a
23	CHD2	chr17:38375341-38375649	Hela-S3	cervix:	n/a	n/a
24	CHD2	chr17:38375385-38375599	K562	blood:	n/a	n/a
25	CHD2	chr17:38374861-38375131	K562	blood:	n/a	n/a
26	CHD2	chr17:38374875-38375619	GM12878	blood:	n/a	n/a
27	CREB1	chr17:38374739-38375933	H1-hESC	embryonic stem cell:	n/a	n/a
28	CREB1	chr17:38375294-38375830	A549	lung:	n/a	n/a
29	CREB1	chr17:38375302-38375615	A549	lung:	n/a	n/a
30	CREB1	chr17:38374748-38375911	GM12878	blood:	n/a	n/a
31	CREB1	chr17:38374799-38375675	ECC-1	luminal epithelium:	n/a	n/a
32	CREB1	chr17:38374862-38375760	H1-hESC	embryonic stem cell:	n/a	n/a
33	CREB1	chr17:38374830-38376296	HepG2	liver:	n/a	n/a
34	CREB1	chr17:38374784-38375641	ECC-1	luminal epithelium:	n/a	n/a
35	CTCF	chr17:38375380-38375530	GM12873	blood:	n/a	chr17:38375470-38375488 chr17:38375473-38375486 chr17:38375471-38375487
36	CTCF	chr17:38375380-38375530	HMF	breast:	n/a	chr17:38375470-38375488 chr17:38375473-38375486 chr17:38375471-38375487
37	CTCF	chr17:38375341-38375617	Spleen_OC	spleen:	n/a	chr17:38375470-38375488 chr17:38375473-38375486 chr17:38375471-38375487
38	CTCF	chr17:38375384-38375567	Hela-S3	cervix:	n/a	chr17:38375470-38375488 chr17:38375473-38375486 chr17:38375471-38375487
39	CTCF	chr17:38375417-38375520	Gliobla	brain:	n/a	chr17:38375470-38375488 chr17:38375473-38375486 chr17:38375471-38375487
40	CTCF	chr17:38375400-38375550	HEK293	kidney:	n/a	chr17:38375470-38375488 chr17:38375473-38375486 chr17:38375471-38375487
41	CTCF	chr17:38375400-38375550	GM12865	blood:	n/a	chr17:38375470-38375488 chr17:38375473-38375486 chr17:38375471-38375487
42	CTCF	chr17:38375340-38375490	HA-sp	spinal cord:	n/a	chr17:38375470-38375488 chr17:38375473-38375486 chr17:38375471-38375487
43	CTCF	chr17:38375400-38375550	HPF	lung:	n/a	chr17:38375470-38375488 chr17:38375473-38375486 chr17:38375471-38375487
44	CTCF	chr17:38375460-38375610	GM12868	blood:	n/a	chr17:38375470-38375488 chr17:38375473-38375486 chr17:38375471-38375487
45	CTCF	chr17:38375400-38375550	GM12869	blood:	n/a	chr17:38375470-38375488 chr17:38375473-38375486 chr17:38375471-38375487
46	CTCF	chr17:38375280-38375430	GM12872	blood:	n/a	n/a
47	CTCF	chr17:38375400-38375550	AG04450	lung:	n/a	chr17:38375470-38375488 chr17:38375473-38375486 chr17:38375471-38375487
48	CTCF	chr17:38375400-38375550	AoAF	blood vessel:	n/a	chr17:38375470-38375488 chr17:38375473-38375486 chr17:38375471-38375487
49	CTCF	chr17:38376100-38376250	HCPEpiC	choroid plexus:	n/a	n/a
50	CTCF	chr17:38375339-38375587	H1-hESC	embryonic stem cell:	n/a	chr17:38375470-38375488 chr17:38375473-38375486 chr17:38375471-38375487

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr17:38374778-38374828	BE2_C	brain:	n/a
2	chr17:38374778-38374828	BE2_C	brain:	n/a
3	chr17:38375747-38375797	IMR90	lung:	fetal
4	chr17:38375747-38375797	GM19239	blood:	n/a
5	chr17:38376239-38376289	IMR90	lung:	fetal
6	chr17:38374778-38374828	HUVEC	blood vessel:	n/a
7	chr17:38375257-38375307	SK-N-SH	brain:	n/a
8	chr17:38375257-38375307	HRPEpiC	eye:	n/a
9	chr17:38375119-38375169	MCF10A-Er-Src	breast:	n/a
10	chr17:38374778-38374828	Hela-S3	cervix:	n/a
11	chr17:38374778-38374828	MCF10A-Er-Src	breast:	n/a
12	chr17:38375510-38375560	BE2_C	brain:	n/a
13	chr17:38376239-38376289	HCPEpiC	choroid plexus:	n/a
14	chr17:38376239-38376289	HPAEpiC	pulmonary alveolar:	n/a
15	chr17:38375257-38375307	PANC-1	pancreas:	n/a
16	chr17:38376239-38376289	MCF10A-Er-Src	breast:	n/a
17	chr17:38375413-38375463	CMK	blood:	n/a
18	chr17:38375459-38375509	MCF-7	breast:	n/a
19	chr17:38375459-38375509	HNPCEpiC	eye:	n/a
20	chr17:38375413-38375463	GM12892	blood:	n/a
21	chr17:38375510-38375560	SAEC	small airway:	n/a
22	chr17:38375199-38375249	AG09319	gingival:	n/a
23	chr17:38375119-38375169	GM19239	blood:	n/a
24	chr17:38375747-38375797	U87	brain:	n/a
25	chr17:38376239-38376289	BJ	skin:	n/a
26	chr17:38375119-38375169	HRPEpiC	eye:	n/a
27	chr17:38375510-38375560	SKMC	muscle:	n/a
28	chr17:38376239-38376289	H1-hESC	embryonic stem cell:	embryo
29	chr17:38376239-38376289	AG04450	lung:	fetal
30	chr17:38375747-38375797	NHBE	bronchial:	n/a
31	chr17:38375441-38375491	HCM	heart:	n/a
32	chr17:38374778-38374828	LNCaP	prostate:	n/a
33	chr17:38375413-38375463	HEK293	kidney:	embryo
34	chr17:38375747-38375797	GM12878	blood:	n/a
35	chr17:38375199-38375249	HEK293	kidney:	embryo
36	chr17:38375119-38375169	HCPEpiC	choroid plexus:	n/a
37	chr17:38375413-38375463	LNCaP	prostate:	n/a
38	chr17:38375441-38375491	RPTEC	kidney:	n/a
39	chr17:38375747-38375797	PANC-1	pancreas:	n/a
40	chr17:38375510-38375560	Hepatocyte	liver:	n/a
41	chr17:38375441-38375491	NT2-D1	testis:	n/a
42	chr17:38376239-38376289	HRE	kidney:	n/a
43	chr17:38374778-38374828	GM12891	blood:	n/a
44	chr17:38375510-38375560	GM06990	blood:	n/a
45	chr17:38375199-38375249	HPAEpiC	pulmonary alveolar:	n/a
46	chr17:38375441-38375491	HIPEpiC	eye:	n/a
47	chr17:38374778-38374828	Hepatocyte	liver:	n/a
48	chr17:38375413-38375463	T-47D	breast:	n/a
49	chr17:38375441-38375491	PFSK-1	brain:	n/a
50	chr17:38375441-38375491	HCF	heart:	n/a

No.	Distal block	Cell Line	Cell type
1	chr17:38374332..38376938-chr17:38443051..38445440,2	MCF-7	breast:
2	chr17:38373931..38375923-chr17:38445660..38448267,2	K562	blood:
3	chr17:38375087..38377704-chr17:38472815..38475239,3	MCF-7	breast:
4	chr17:38278214..38280293-chr17:38374121..38375969,2	K562	blood:
5	chr14:71374178..71375131-chr17:38377088..38378038,2	Hela-S3	cervix:
6	chr17:38374494..38376026-chr17:38472428..38474743,2	K562	blood:
7	chr17:38374494..38377034-chr17:38473243..38475629,2	K562	blood:
8	chr17:38374160..38377020-chr17:38442777..38445786,6	K562	blood:
9	chr17:38346506..38348012-chr17:38375510..38377087,2	MCF-7	breast:
10	chr17:38335879..38338134-chr17:38374200..38376894,2	MCF-7	breast:
11	chr17:38374207..38376996-chr17:38442281..38444578,5	K562	blood:
12	chr17:38375504..38376129-chr6:80713334..80714172,2	Hela-S3	cervix:

Variant related genes	Relation type
WIPF2	TF binding region
WIPF2	CpG island
ENSG00000094804	chromatin interactions
ENSG00000108352	chromatin interactions
ENSG00000188895	chromatin interactions
ENSG00000131759	chromatin interactions
ENSG00000112742	chromatin interactions
ENSG00000100731	chromatin interactions

Extended variants
information (count: 96 )
Associated
traits (count: 125 )

Variant overlapped rSNPs/rCNVs (count:96 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs545328350	chr17:38374657-38374658	Active TSS Enhancers Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
2	rs141881923	chr17:38374697-38374698	Active TSS Enhancers Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
3	rs527482839	chr17:38374703-38374704	Active TSS Enhancers Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
4	rs145639349	chr17:38374759-38374760	Active TSS Enhancers Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
5	rs185004526	chr17:38374761-38374762	Active TSS Enhancers Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
6	rs374050958	chr17:38374845-38374846	Active TSS Enhancers Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
7	rs550273580	chr17:38374852-38374853	Active TSS Enhancers Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
8	rs571660533	chr17:38374855-38374856	Active TSS Enhancers Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
9	rs538644761	chr17:38374859-38374860	Active TSS Enhancers Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
10	rs548075307	chr17:38374980-38374981	Active TSS Enhancers Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
11	rs566216888	chr17:38375015-38375016	Active TSS Enhancers Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
12	rs377676909	chr17:38375059-38375060	Active TSS Enhancers Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
13	rs35430178	chr17:38375122-38375123	Active TSS Enhancers Flanking Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
14	rs536467082	chr17:38375164-38375165	Active TSS Enhancers Flanking Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
15	rs540452342	chr17:38375171-38375172	Active TSS Enhancers Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
16	rs140101802	chr17:38375172-38375173	Active TSS Enhancers Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
17	rs539337351	chr17:38375181-38375182	Active TSS Enhancers Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
18	rs189075958	chr17:38375182-38375183	Active TSS Enhancers Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
19	rs114950975	chr17:38375250-38375251	Active TSS Enhancers Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
20	rs537596654	chr17:38375318-38375319	Active TSS Enhancers Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
21	rs555978013	chr17:38375376-38375377	Active TSS Enhancers Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
22	rs147729599	chr17:38375400-38375401	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
23	rs72836641	chr17:38375402-38375403	Active TSS Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs572575789	chr17:38375408-38375409	Active TSS Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
25	rs560418124	chr17:38375411-38375412	Active TSS Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
26	rs200198310	chr17:38375413-38375414	Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
27	rs572211646	chr17:38375417-38375418	Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
28	rs373976903	chr17:38375454-38375455	Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
29	rs542927293	chr17:38375471-38375472	Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
30	rs117369210	chr17:38375496-38375497	Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
31	rs531528101	chr17:38375545-38375546	Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
32	rs542122273	chr17:38375620-38375621	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
33	rs368567525	chr17:38375621-38375622	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
34	rs71152656	chr17:38375640-38375641	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
35	rs535395784	chr17:38375646-38375647	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
36	rs60253561	chr17:38375651-38375652	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
37	rs565192365	chr17:38375652-38375653	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
38	rs532561852	chr17:38375653-38375654	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
39	rs547441940	chr17:38375671-38375672	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
40	rs566052082	chr17:38375687-38375688	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
41	rs530357236	chr17:38375753-38375754	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	TF binding region CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
42	rs377384723	chr17:38375902-38375903	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
43	rs548470050	chr17:38375956-38375957	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
44	rs199736705	chr17:38375978-38375979	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
45	rs149190468	chr17:38376036-38376037	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
46	rs543110970	chr17:38376047-38376048	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
47	rs181913217	chr17:38376136-38376137	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs561352614	chr17:38376139-38376140	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs556228541	chr17:38376160-38376161	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs571225006	chr17:38376162-38376163	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:125)

Disease	PMID	Source
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
Melanoma	18172304	CNVD
Moyamoya disease	22323933	CNVD
Oral squamous cell carcinoma	17134496	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
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Hodgkin''s lymphoma	17606441	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute myeloid leukemia	20729466	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
lymphocytic leukemia	21291569	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
Chronic lymphocytic leukemia	21546498	CNVD
Gastric cancer	24379144	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	16608533	CNVD
Breast cancer	17457667	CNVD
Breast cancer	16951389	CNVD
Basal cell lymphoma	17053054	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Acute myeloid leukemia	21251322	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21364760	CNVD
Lung cancer	18438408	CNVD
Breast cancer	16620391	CNVD
Breast cancer	21509527	CNVD
Breast cancer	22048815	CNVD
Breast cancer	17603634	CNVD
Follicular lymphoma	20505157	CNVD
Non-small cell lung cancer	20864512	CNVD
Cancer	21183584	CNVD
Cervical cancer	21062161	CNVD
Breast cancer	20953835	CNVD
Thyroid cancer	19087340	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Sezary syndrome	18413736	CNVD
Urothelial carcinoma	21177765	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Myelofibrosis	22110671	CNVD
Disease	22962312	CNVD
Mental retardation	20152051	CNVD
Mental retardation	19951919	CNVD
Mental retardation	22817714	CNVD
Mental retardation	21956041	CNVD
Brain cancer	19584924	CNVD
Glioblastoma multiforme	22286061	CNVD
Schizophrenia	21399695	CNVD
Non-syndromic sensorineural hearing loss	19165922	CNVD
Prader-willi syndrome	20588305	CNVD
17q21.31 microdeletion syndrome	16940994	CNVD
Non-syndromic sensorineural hearing loss	21084979	CNVD
17q21.31 microdeletion syndrome	22283845	CNVD
Intellectual disability	22194194	CNVD
17q21.31 microdeletion syndrome	20606400	CNVD
17q21.31 microdeletion syndrome	18628315	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Hirschsprung''s Disease	21712996	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
TAR Syndrome	17847015	CNVD
Neuroblastoma	18923191	CNVD
Breast cancer	20409316	CNVD
HIV/AIDS	18360285	CNVD
HIV/AIDS	17330138	CNVD
Systemic lupus erythematosus	19287148	CNVD
Frontotemporal lobar degeneration	19640594	CNVD
HIV/AIDS	17008540	CNVD
Breast cancer	17850661	CNVD
Breast cancer	19261255	CNVD
Lung cancer	16773561	CNVD
Neurocytoma	17123091	CNVD
Central neurocytomas	17123091	CNVD
Basal-like breast cancer	18066063	CNVD
Breast cancer	20031965	CNVD
Colorectal cancer	19287155	CNVD
Hereditary breast	19566914	CNVD
Ovarian cancer	19047089	CNVD
Ovarian cancer	19566914	CNVD
Triple-negative breast cancer	18950515	CNVD
Breast cancer	16846527	CNVD
Lung cancer	21203850	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:486 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr17:38366800-38375000	Weak transcription	HSMM	muscle
2	chr17:38369600-38374800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
3	chr17:38373200-38374800	Weak transcription	Monocytes-CD14+_RO01746	blood
4	chr17:38373400-38374800	Weak transcription	Primary monocytes fromperipheralblood	blood
5	chr17:38374000-38375000	Enhancers	Cortex derived primary cultured neurospheres	brain
6	chr17:38374000-38375000	Enhancers	Placenta	Placenta
7	chr17:38374200-38374800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
8	chr17:38374200-38374800	Weak transcription	Spleen	Spleen
9	chr17:38374200-38375000	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
10	chr17:38374200-38375000	Enhancers	HepG2	liver
11	chr17:38374400-38374800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
12	chr17:38374400-38374800	Enhancers	Primary B cells from peripheral blood	blood
13	chr17:38374400-38374800	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
14	chr17:38374400-38375000	Flanking Active TSS	Brain Anterior Caudate	brain
15	chr17:38374400-38375000	Enhancers	Hela-S3	cervix
16	chr17:38374400-38375000	Enhancers	HMEC	breast
17	chr17:38374600-38374800	Enhancers	H9 Cell Line	embryonic stem cell
18	chr17:38374600-38374800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
19	chr17:38374600-38374800	Enhancers	HUES48 Cell Line	embryonic stem cell
20	chr17:38374600-38374800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
21	chr17:38374600-38374800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
22	chr17:38374600-38374800	Enhancers	Primary T cells from cord blood	blood
23	chr17:38374600-38374800	Enhancers	Primary T cells fromperipheralblood	blood
24	chr17:38374600-38374800	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
25	chr17:38374600-38374800	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
26	chr17:38374600-38374800	Enhancers	Primary T helper cells fromperipheralblood	blood
27	chr17:38374600-38374800	Enhancers	Primary T regulatory cells fromperipheralblood	blood
28	chr17:38374600-38374800	Enhancers	Primary T killer naive cells fromperipheralblood	blood
29	chr17:38374600-38374800	Enhancers	Primary T killer memory cells from peripheral blood	blood
30	chr17:38374600-38374800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
31	chr17:38374600-38374800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
32	chr17:38374600-38374800	Enhancers	Muscle Satellite Cultured Cells	--
33	chr17:38374600-38374800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
34	chr17:38374600-38374800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
35	chr17:38374600-38374800	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
36	chr17:38374600-38374800	Enhancers	Duodenum Smooth Muscle	Duodenum
37	chr17:38374600-38374800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
38	chr17:38374600-38374800	Enhancers	Fetal Brain Male	brain
39	chr17:38374600-38374800	Flanking Active TSS	Fetal Brain Female	brain
40	chr17:38374600-38374800	Flanking Active TSS	Pancreatic Islets	Pancreatic Islet
41	chr17:38374600-38374800	Enhancers	A549	lung
42	chr17:38374600-38374800	Enhancers	Dnd41	blood
43	chr17:38374600-38374800	Enhancers	GM12878-XiMat	blood
44	chr17:38374600-38374800	Enhancers	NH-A	brain
45	chr17:38374600-38374800	Enhancers	NHLF	lung
46	chr17:38374600-38375000	Flanking Active TSS	Primary T helper naive cells from peripheral blood	blood
47	chr17:38374600-38375000	Flanking Active TSS	Primary T helper naive cells fromperipheralblood	blood
48	chr17:38374600-38375000	Flanking Active TSS	Primary T helper memory cells from peripheral blood 1	blood
49	chr17:38374600-38375000	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
50	chr17:38374600-38375000	Flanking Active TSS	Brain Hippocampus Middle	brain

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