Variant report

Variant	esv1795575
Chromosome Location	chr17:37974075-38041762
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1249)
CpG islands
(count:795)
Chromatin interactive
region (count:23)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1249 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr17:37984640-37985086	HepG2	liver:	n/a	n/a
2	ARID3A	chr17:38028945-38029299	HepG2	liver:	n/a	n/a
3	ARID3A	chr17:38020428-38020582	HepG2	liver:	n/a	n/a
4	ARID3A	chr17:38008553-38008928	K562	blood:	n/a	n/a
5	ATF2	chr17:38023105-38024425	GM12878	blood:	n/a	n/a
6	ATF2	chr17:37999211-38000194	GM12878	blood:	n/a	n/a
7	ATF2	chr17:38021060-38022082	GM12878	blood:	n/a	n/a
8	ATF2	chr17:38020128-38021054	GM12878	blood:	n/a	n/a
9	ATF2	chr17:38021011-38022016	GM12878	blood:	n/a	n/a
10	ATF2	chr17:38020154-38020868	GM12878	blood:	n/a	n/a
11	ATF2	chr17:38020263-38020561	H1-hESC	embryonic stem cell:	n/a	n/a
12	ATF2	chr17:38022555-38024496	GM12878	blood:	n/a	n/a
13	BACH1	chr17:38006082-38006139	K562	blood:	n/a	n/a
14	BACH1	chr17:38020382-38020647	H1-hESC	embryonic stem cell:	n/a	n/a
15	BATF	chr17:37999747-38000074	GM12878	blood:	n/a	n/a
16	BATF	chr17:38021710-38022035	GM12878	blood:	n/a	n/a
17	BATF	chr17:38023205-38024346	GM12878	blood:	n/a	chr17:38023358-38023368
18	BATF	chr17:38021626-38022071	GM12878	blood:	n/a	n/a
19	BATF	chr17:38020268-38020634	GM12878	blood:	n/a	n/a
20	BATF	chr17:38023175-38023725	GM12878	blood:	n/a	chr17:38023358-38023368
21	BATF	chr17:38021134-38021514	GM12878	blood:	n/a	n/a
22	BCL11A	chr17:38020283-38020775	GM12878	blood:	n/a	n/a
23	BCL11A	chr17:38023812-38024186	GM12878	blood:	n/a	chr17:38023905-38023914
24	BCL11A	chr17:38023155-38024576	GM12878	blood:	n/a	chr17:38023905-38023914 chr17:38024227-38024236 chr17:38024411-38024424
25	BCL11A	chr17:38021611-38021996	GM12878	blood:	n/a	n/a
26	BCL11A	chr17:38021138-38021425	GM12878	blood:	n/a	n/a
27	BCL11A	chr17:38023373-38023765	GM12878	blood:	n/a	n/a
28	BCL3	chr17:38021272-38022083	GM12878	blood:	n/a	n/a
29	BCL3	chr17:38020312-38020683	GM12878	blood:	n/a	n/a
30	BCL3	chr17:38020213-38020792	GM12878	blood:	n/a	n/a
31	BCL3	chr17:38023200-38024490	GM12878	blood:	n/a	chr17:38023905-38023914 chr17:38024227-38024236 chr17:38024411-38024424
32	BCLAF1	chr17:38023174-38024636	GM12878	blood:	n/a	chr17:38023905-38023914 chr17:38024227-38024236 chr17:38024411-38024424
33	BCLAF1	chr17:38019864-38022044	GM12878	blood:	n/a	n/a
34	BCLAF1	chr17:38023108-38024567	GM12878	blood:	n/a	chr17:38023905-38023914 chr17:38024227-38024236 chr17:38024411-38024424
35	BCLAF1	chr17:37999571-38000078	GM12878	blood:	n/a	n/a
36	BCLAF1	chr17:38021114-38022005	GM12878	blood:	n/a	n/a
37	BCLAF1	chr17:37999056-38000188	GM12878	blood:	n/a	n/a
38	BCLAF1	chr17:38016785-38017269	GM12878	blood:	n/a	n/a
39	BCLAF1	chr17:38008392-38008990	GM12878	blood:	n/a	n/a
40	BCLAF1	chr17:38020136-38020892	GM12878	blood:	n/a	n/a
41	BHLHE40	chr17:38021185-38022065	GM12878	blood:	n/a	n/a
42	BHLHE40	chr17:38023169-38024618	GM12878	blood:	n/a	chr17:38024360-38024376 chr17:38024076-38024089 chr17:38024072-38024093
43	BHLHE40	chr17:38020305-38020614	HepG2	liver:	n/a	chr17:38020503-38020519
44	BHLHE40	chr17:38012492-38012854	GM12878	blood:	n/a	n/a
45	BHLHE40	chr17:38020320-38020646	K562	blood:	n/a	chr17:38020503-38020519
46	BHLHE40	chr17:37974643-37975121	GM12878	blood:	n/a	n/a
47	BHLHE40	chr17:38020161-38020755	GM12878	blood:	n/a	chr17:38020503-38020519
48	BRCA1	chr17:38022555-38022699	GM12878	blood:	n/a	n/a
49	BRCA1	chr17:38020442-38020635	H1-hESC	embryonic stem cell:	n/a	n/a
50	BRCA1	chr17:38023750-38023954	GM12878	blood:	n/a	n/a

(count:795 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr17:38024146-38024196	HRE	kidney:	n/a
2	chr17:38020644-38020694	Jurkat	blood:	n/a
3	chr17:38024146-38024196	HRE	kidney:	n/a
4	chr17:38020644-38020694	Jurkat	blood:	n/a
5	chr17:38023480-38023530	HAEpiC	amniotic membrane:	n/a
6	chr17:38021651-38021701	PrEC	prostate:	n/a
7	chr17:38024636-38024686	HL-60	blood:	n/a
8	chr17:38017814-38017864	GM12892	blood:	n/a
9	chr17:38021651-38021701	HUVEC	blood vessel:	n/a
10	chr17:38020667-38020717	HEEpiC	esophagus:	n/a
11	chr17:38024636-38024686	MCF10A-Er-Src	breast:	n/a
12	chr17:38024394-38024444	HCT-116	colon:	n/a
13	chr17:38024146-38024196	LNCaP	prostate:	n/a
14	chr17:38017814-38017864	ECC-1	luminal epithelium:	n/a
15	chr17:38020344-38020394	PFSK-1	brain:	n/a
16	chr17:38020344-38020394	AG04449	skin:	fetal
17	chr17:38023480-38023530	RPTEC	kidney:	n/a
18	chr17:38021651-38021701	NH-A	brain:	n/a
19	chr17:38020644-38020694	MCF-7	breast:	n/a
20	chr17:38024636-38024686	RPTEC	kidney:	n/a
21	chr17:38020606-38020656	ProgFib	skin:	n/a
22	chr17:38024636-38024686	SK-N-SH_RA	brain:	n/a
23	chr17:38024146-38024196	AG09319	gingival:	n/a
24	chr17:38024146-38024196	SK-N-SH_RA	brain:	n/a
25	chr17:38024394-38024444	HAEpiC	amniotic membrane:	n/a
26	chr17:38023679-38023729	U87	brain:	n/a
27	chr17:38020667-38020717	HCM	heart:	n/a
28	chr17:38020667-38020717	NH-A	brain:	n/a
29	chr17:38020644-38020694	SKMC	muscle:	n/a
30	chr17:38028394-38028444	AG04450	lung:	fetal
31	chr17:38020344-38020394	GM12892	blood:	n/a
32	chr17:38021651-38021701	HPAEpiC	pulmonary alveolar:	n/a
33	chr17:38028394-38028444	Jurkat	blood:	n/a
34	chr17:38023679-38023729	SK-N-MC	brain:	n/a
35	chr17:38028394-38028444	ProgFib	skin:	n/a
36	chr17:38028394-38028444	GM19239	blood:	n/a
37	chr17:38023480-38023530	HepG2	liver:	n/a
38	chr17:38023679-38023729	BE2_C	brain:	n/a
39	chr17:38020344-38020394	T-47D	breast:	n/a
40	chr17:38020606-38020656	HCT-116	colon:	n/a
41	chr17:38017814-38017864	HPAEpiC	pulmonary alveolar:	n/a
42	chr17:38024636-38024686	HIPEpiC	eye:	n/a
43	chr17:38023993-38024043	GM12891	blood:	n/a
44	chr17:38024636-38024686	HRCEpiC	kidney:	n/a
45	chr17:38020667-38020717	SAEC	small airway:	n/a
46	chr17:38028394-38028444	HMEC	breast:	n/a
47	chr17:38021651-38021701	HRPEpiC	eye:	n/a
48	chr17:38020344-38020394	HMEC	breast:	n/a
49	chr17:38020344-38020394	AG04450	lung:	fetal
50	chr17:38023679-38023729	NHBE	bronchial:	n/a

(count:23 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr17:38009036..38011369-chr17:38074696..38077048,2	K562	blood:
2	chr17:38031917..38033565-chr17:38036267..38038135,2	K562	blood:
3	chr17:38016485..38022109-chr17:38022345..38027890,7	K562	blood:
4	chr17:37980608..37984471-chr17:37984850..37987192,3	K562	blood:
5	chr17:38027089..38030727-chr17:38135584..38137903,4	MCF-7	breast:
6	chr17:38028899..38029611-chr17:38169830..38170569,2	MCF-7	breast:
7	chr17:38016485..38022109-chr17:38022345..38027890,7	K562	blood:
8	chr17:38031917..38033565-chr17:38036267..38038135,2	K562	blood:
9	chr17:37978424..37980112-chr17:38107868..38109558,2	K562	blood:
10	chr17:37997862..38000754-chr17:38065312..38067694,2	K562	blood:
11	chr17:37777964..37778788-chr17:38020511..38021070,2	MCF-7	breast:
12	chr17:37980608..37984471-chr17:37984850..37987192,3	K562	blood:
13	chr17:38039742..38042523-chr17:38137576..38139684,2	K562	blood:
14	chr17:37993320..37996437-chr17:37998688..38001239,3	K562	blood:
15	chr17:38028703..38029243-chr17:38136410..38137027,2	MCF-7	breast:
16	chr17:37777900..37778761-chr17:37991112..37991981,2	K562	blood:
17	chr17:37912256..37913081-chr17:38028636..38029533,2	MCF-7	breast:
18	chr17:38022690..38024941-chr17:38027177..38028935,2	K562	blood:
19	chr17:38016155..38020243-chr17:38021178..38026655,8	K562	blood:
20	chr17:38004767..38008555-chr17:38017604..38021491,3	K562	blood:
21	chr17:38027253..38029353-chr17:38058744..38061451,2	K562	blood:
22	chr17:37893210..37895843-chr17:38018530..38020744,2	MCF-7	breast:
23	chr17:38038617..38042523-chr17:38137576..38140223,3	K562	blood:

No data

Variant related genes	Relation type
ZPBP2	TF binding region
IKZF3	TF binding region
ENSG00000226117	TF binding region
KRT8P34	TF binding region
ZPBP2	CpG island
IKZF3	CpG island
ENSG00000226117	CpG island
KRT8P34	CpG island
ENSG00000226117	chromatin interactions
ENSG00000186075	chromatin interactions
ENSG00000161405	chromatin interactions
ENSG00000108344	chromatin interactions
ENSG00000073605	chromatin interactions
ENSG00000141738	chromatin interactions

Extended variants
information (count: 2089 )
Associated
traits (count: 128 )

Variant overlapped rSNPs/rCNVs (count:2089 , 50 per page) page: 1 2 3 4 5 6 7 ... 42

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs567207051	chr17:37974082-37974083	Strong transcription Genic enhancers Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs537465241	chr17:37974101-37974102	Strong transcription Genic enhancers Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs182409638	chr17:37974172-37974173	Strong transcription Genic enhancers Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs577846151	chr17:37974182-37974183	Strong transcription Genic enhancers Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs556760210	chr17:37974209-37974210	Strong transcription Genic enhancers Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs553550161	chr17:37974280-37974281	Strong transcription Genic enhancers Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs371422522	chr17:37974293-37974294	Strong transcription Genic enhancers Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs571916877	chr17:37974295-37974296	Strong transcription Genic enhancers Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs542663856	chr17:37974304-37974305	Strong transcription Genic enhancers Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs185152198	chr17:37974307-37974308	Strong transcription Genic enhancers Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs189920961	chr17:37974329-37974330	Strong transcription Genic enhancers Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs543435911	chr17:37974340-37974341	Strong transcription Genic enhancers Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs565307731	chr17:37974369-37974370	Strong transcription Genic enhancers Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs532691270	chr17:37974488-37974489	Strong transcription Genic enhancers Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs548148970	chr17:37974494-37974495	Strong transcription Genic enhancers Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs9913957	chr17:37974499-37974500	Strong transcription Genic enhancers Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
17	rs530322735	chr17:37974525-37974526	Strong transcription Genic enhancers Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs567089894	chr17:37974535-37974536	Strong transcription Genic enhancers Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs112274637	chr17:37974634-37974635	Genic enhancers Enhancers Weak transcription Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
20	rs181171089	chr17:37974652-37974653	Genic enhancers Enhancers Weak transcription Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
21	rs185626118	chr17:37974654-37974655	Genic enhancers Enhancers Weak transcription Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
22	rs532834948	chr17:37974685-37974686	Genic enhancers Enhancers Weak transcription Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
23	rs549492139	chr17:37974734-37974735	Genic enhancers Enhancers Weak transcription Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
24	rs146760210	chr17:37974745-37974746	Genic enhancers Enhancers Weak transcription Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
25	rs538539130	chr17:37974774-37974775	Genic enhancers Enhancers Weak transcription Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
26	rs553652892	chr17:37974807-37974808	Enhancers Transcr. at gene 5' and 3' Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs191566775	chr17:37974813-37974814	Enhancers Transcr. at gene 5' and 3' Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs552289920	chr17:37974828-37974829	Enhancers Transcr. at gene 5' and 3' Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs536054915	chr17:37974840-37974841	Enhancers Transcr. at gene 5' and 3' Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs575062871	chr17:37974876-37974877	Enhancers Transcr. at gene 5' and 3' Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs569189949	chr17:37974938-37974939	Enhancers Transcr. at gene 5' and 3' Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs538366863	chr17:37974983-37974984	Enhancers Transcr. at gene 5' and 3' Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs140386398	chr17:37975009-37975010	Enhancers Transcr. at gene 5' and 3' Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs543942922	chr17:37975012-37975013	Enhancers Transcr. at gene 5' and 3' Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs548729326	chr17:37975043-37975044	Enhancers Transcr. at gene 5' and 3' Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs368646217	chr17:37975109-37975110	Enhancers Transcr. at gene 5' and 3' Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs150358009	chr17:37975129-37975130	Enhancers Transcr. at gene 5' and 3' Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs577178730	chr17:37975169-37975170	Enhancers Transcr. at gene 5' and 3' Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs375560175	chr17:37975212-37975213	Enhancers Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
40	rs113765011	chr17:37975213-37975214	Enhancers Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
41	rs113897057	chr17:37975214-37975215	Enhancers Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
42	rs67447905	chr17:37975215-37975216	Enhancers Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
43	rs71152606	chr17:37975218-37975219	Enhancers Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
44	rs75427961	chr17:37975219-37975220	Enhancers Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
45	rs541699018	chr17:37975301-37975302	Enhancers Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
46	rs560111628	chr17:37975313-37975314	Enhancers Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
47	rs138034506	chr17:37975349-37975350	Enhancers Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
48	rs373634051	chr17:37975358-37975359	Enhancers Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
49	rs542429862	chr17:37975373-37975374	Enhancers Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
50	rs183415777	chr17:37975439-37975440	Enhancers Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:128)

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
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
Chronic lymphocytic leukemia	21546498	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
Acute myeloid leukemia	21251322	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21364760	CNVD
Lung cancer	18438408	CNVD
Breast cancer	16620391	CNVD
Prostate cancer	18632612	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
Cancer	20164920	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	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:924 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr17:37970400-37974600	Strong transcription	Primary B cells from cord blood	blood
2	chr17:37970400-37978600	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
3	chr17:37970600-37977600	Enhancers	Primary T helper cells PMA-I stimulated	--
4	chr17:37971000-37974800	Weak transcription	Fetal Thymus	thymus
5	chr17:37971400-37974200	Weak transcription	Thymus	Thymus
6	chr17:37971400-37974600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
7	chr17:37972600-37974800	Enhancers	Primary T helper naive cells fromperipheralblood	blood
8	chr17:37973200-37975000	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
9	chr17:37973200-37976800	Enhancers	Primary T helper cells fromperipheralblood	blood
10	chr17:37973200-37978200	Enhancers	Primary T killer memory cells from peripheral blood	blood
11	chr17:37973400-37974600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
12	chr17:37973400-37975200	Enhancers	Primary T cells from cord blood	blood
13	chr17:37973400-37978400	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
14	chr17:37973600-37976600	Enhancers	Primary T helper naive cells from peripheral blood	blood
15	chr17:37973800-37977600	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
16	chr17:37973800-37978400	Enhancers	Primary T killer naive cells fromperipheralblood	blood
17	chr17:37973800-37979200	Genic enhancers	Primary B cells from peripheral blood	blood
18	chr17:37974000-37974600	Weak transcription	Primary T cells fromperipheralblood	blood
19	chr17:37974000-37974600	Genic enhancers	GM12878-XiMat	blood
20	chr17:37974000-37977800	Enhancers	Primary T regulatory cells fromperipheralblood	blood
21	chr17:37974200-37975800	Enhancers	Thymus	Thymus
22	chr17:37974200-37976600	Enhancers	Dnd41	blood
23	chr17:37974600-37974800	Genic enhancers	Primary B cells from cord blood	blood
24	chr17:37974600-37976000	Enhancers	HMEC	breast
25	chr17:37974600-37976400	Transcr. at gene 5' and 3'	GM12878-XiMat	blood
26	chr17:37974600-37976400	Enhancers	NHEK	skin
27	chr17:37974600-37977000	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
28	chr17:37974600-37978400	Enhancers	Primary T cells fromperipheralblood	blood
29	chr17:37974600-37978400	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
30	chr17:37974800-37975000	Flanking Active TSS	Primary T helper naive cells fromperipheralblood	blood
31	chr17:37974800-37975200	Transcr. at gene 5' and 3'	Primary B cells from cord blood	blood
32	chr17:37974800-37975200	Genic enhancers	Fetal Thymus	thymus
33	chr17:37974800-37976000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
34	chr17:37974800-37977000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
35	chr17:37975000-37975200	Enhancers	Primary T helper naive cells fromperipheralblood	blood
36	chr17:37975000-37975400	Flanking Active TSS	Primary T helper 17 cells PMA-I stimulated	--
37	chr17:37975200-37975400	Flanking Active TSS	Primary T helper naive cells fromperipheralblood	blood
38	chr17:37975200-37975800	Flanking Active TSS	Primary T cells from cord blood	blood
39	chr17:37975200-37977200	Enhancers	Fetal Thymus	thymus
40	chr17:37975200-37978800	Genic enhancers	Primary B cells from cord blood	blood
41	chr17:37975400-37975600	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
42	chr17:37975400-37975600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
43	chr17:37975400-37976000	Enhancers	Primary hematopoietic stem cells	blood
44	chr17:37975400-37978200	Enhancers	Primary T helper naive cells fromperipheralblood	blood
45	chr17:37975600-37975800	Flanking Active TSS	Primary T helper 17 cells PMA-I stimulated	--
46	chr17:37975600-37975800	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
47	chr17:37975600-37975800	Enhancers	Duodenum Mucosa	Duodenum
48	chr17:37975600-37977200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
49	chr17:37975800-37976800	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
50	chr17:37975800-37978600	Enhancers	Primary T cells from cord blood	blood

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