Variant report

Variant	nsv543321
Chromosome Location	chr17:34285312-34365313
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1429)
CpG islands
(count:1650)
Chromatin interactive
region (count:21)
LncRNA
region (count:23)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1429 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr17:34296546-34296837	HepG2	liver:	n/a	n/a
2	ARID3A	chr17:34296539-34296811	K562	blood:	n/a	n/a
3	ARID3A	chr17:34308475-34309426	HepG2	liver:	n/a	n/a
4	ARID3A	chr17:34328959-34329418	HepG2	liver:	n/a	n/a
5	ARID3A	chr17:34327658-34328409	HepG2	liver:	n/a	n/a
6	ARID3A	chr17:34334077-34334506	HepG2	liver:	n/a	n/a
7	ARID3A	chr17:34302631-34302635	HepG2	liver:	n/a	n/a
8	ARID3A	chr17:34299996-34301342	HepG2	liver:	n/a	n/a
9	ARID3A	chr17:34307009-34307334	HepG2	liver:	n/a	n/a
10	ARID3A	chr17:34303181-34303192	K562	blood:	n/a	n/a
11	ARID3A	chr17:34318006-34318439	HepG2	liver:	n/a	chr17:34318073-34318089
12	ATF1	chr17:34341720-34341879	K562	blood:	n/a	n/a
13	ATF1	chr17:34292558-34292617	K562	blood:	n/a	n/a
14	ATF1	chr17:34361855-34362036	K562	blood:	n/a	n/a
15	ATF1	chr17:34361266-34361504	K562	blood:	n/a	n/a
16	ATF2	chr17:34329572-34330112	GM12878	blood:	n/a	n/a
17	ATF2	chr17:34329668-34330078	GM12878	blood:	n/a	n/a
18	BATF	chr17:34361202-34361551	GM12878	blood:	n/a	n/a
19	BATF	chr17:34329548-34330108	GM12878	blood:	n/a	n/a
20	BATF	chr17:34329664-34330037	GM12878	blood:	n/a	n/a
21	BATF	chr17:34322349-34322661	GM12878	blood:	n/a	n/a
22	BATF	chr17:34361127-34361501	GM12878	blood:	n/a	n/a
23	BATF	chr17:34323534-34323954	GM12878	blood:	n/a	chr17:34323758-34323769
24	BATF	chr17:34328155-34328421	GM12878	blood:	n/a	n/a
25	BCL11A	chr17:34323577-34323941	GM12878	blood:	n/a	n/a
26	BCL11A	chr17:34361182-34361479	GM12878	blood:	n/a	n/a
27	BCL11A	chr17:34329596-34330102	GM12878	blood:	n/a	n/a
28	BCL11A	chr17:34304610-34304854	GM12878	blood:	n/a	n/a
29	BCL11A	chr17:34329665-34329981	GM12878	blood:	n/a	n/a
30	BCL11A	chr17:34361131-34361551	GM12878	blood:	n/a	n/a
31	BCL11A	chr17:34322415-34322588	GM12878	blood:	n/a	n/a
32	BCL3	chr17:34329660-34329979	GM12878	blood:	n/a	n/a
33	BHLHE40	chr17:34329682-34330135	GM12878	blood:	n/a	n/a
34	BHLHE40	chr17:34336354-34336581	K562	blood:	n/a	n/a
35	BHLHE40	chr17:34300106-34300772	HepG2	liver:	n/a	n/a
36	BHLHE40	chr17:34308959-34309395	HepG2	liver:	n/a	n/a
37	BHLHE40	chr17:34313471-34313719	K562	blood:	n/a	n/a
38	BHLHE40	chr17:34296561-34296772	K562	blood:	n/a	n/a
39	BHLHE40	chr17:34304652-34304849	GM12878	blood:	n/a	n/a
40	BHLHE40	chr17:34299616-34301201	HepG2	liver:	n/a	n/a
41	BHLHE40	chr17:34327796-34328088	HepG2	liver:	n/a	n/a
42	BHLHE40	chr17:34336322-34336547	HepG2	liver:	n/a	n/a
43	BHLHE40	chr17:34327737-34328022	HepG2	liver:	n/a	n/a
44	BHLHE40	chr17:34361203-34361578	GM12878	blood:	n/a	n/a
45	BHLHE40	chr17:34327631-34328115	HepG2	liver:	n/a	n/a
46	BHLHE40	chr17:34328950-34329391	HepG2	liver:	n/a	n/a
47	BRCA1	chr17:34296602-34296820	Hela-S3	cervix:	n/a	n/a
48	BRCA1	chr17:34328982-34329177	HepG2	liver:	n/a	n/a
49	CBX3	chr17:34336124-34336681	K562	blood:	n/a	n/a
50	CEBPB	chr17:34307064-34307263	HepG2	liver:	n/a	n/a

(count:1650 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr17:34329899-34329949	ECC-1	luminal epithelium:	n/a
2	chr17:34314768-34314818	AG09319	gingival:	n/a
3	chr17:34346381-34346431	A549	lung:	n/a
4	chr17:34329899-34329949	ECC-1	luminal epithelium:	n/a
5	chr17:34314768-34314818	AG09319	gingival:	n/a
6	chr17:34346381-34346431	A549	lung:	n/a
7	chr17:34329080-34329130	GM12892	blood:	n/a
8	chr17:34308465-34308515	GM12878	blood:	n/a
9	chr17:34344416-34344466	BJ	skin:	n/a
10	chr17:34344416-34344466	HUVEC	blood vessel:	n/a
11	chr17:34346381-34346431	SKMC	muscle:	n/a
12	chr17:34328396-34328446	MCF10A-Er-Src	breast:	n/a
13	chr17:34304462-34304512	BE2_C	brain:	n/a
14	chr17:34346433-34346483	GM12891	blood:	n/a
15	chr17:34308137-34308187	HRPEpiC	eye:	n/a
16	chr17:34346433-34346483	NT2-D1	testis:	n/a
17	chr17:34309129-34309179	HIPEpiC	eye:	n/a
18	chr17:34315074-34315124	RPTEC	kidney:	n/a
19	chr17:34314768-34314818	AG04450	lung:	fetal
20	chr17:34311861-34311911	LNCaP	prostate:	n/a
21	chr17:34309207-34309257	Caco-2	colon:	n/a
22	chr17:34330056-34330106	AG04450	lung:	fetal
23	chr17:34344995-34345045	HL-60	blood:	n/a
24	chr17:34314511-34314561	SK-N-SH_RA	brain:	n/a
25	chr17:34345136-34345186	HepG2	liver:	n/a
26	chr17:34309129-34309179	AG09309	skin:	n/a
27	chr17:34315074-34315124	HRPEpiC	eye:	n/a
28	chr17:34314511-34314561	HepG2	liver:	n/a
29	chr17:34308465-34308515	T-47D	breast:	n/a
30	chr17:34329201-34329251	HEK293	kidney:	embryo
31	chr17:34314511-34314561	SKMC	muscle:	n/a
32	chr17:34329899-34329949	HAEpiC	amniotic membrane:	n/a
33	chr17:34309577-34309627	MCF10A-Er-Src	breast:	n/a
34	chr17:34314768-34314818	HMEC	breast:	n/a
35	chr17:34308567-34308617	AoSMC	blood vessel:	n/a
36	chr17:34329201-34329251	CMK	blood:	n/a
37	chr17:34308465-34308515	NB4	blood:	n/a
38	chr17:34304462-34304512	AG04450	lung:	fetal
39	chr17:34345172-34345222	Hela-S3	cervix:	n/a
40	chr17:34314511-34314561	PFSK-1	brain:	n/a
41	chr17:34346433-34346483	H1-hESC	embryonic stem cell:	embryo
42	chr17:34308137-34308187	GM06990	blood:	n/a
43	chr17:34314511-34314561	AG04450	lung:	fetal
44	chr17:34309207-34309257	GM06990	blood:	n/a
45	chr17:34329201-34329251	Hela-S3	cervix:	n/a
46	chr17:34329080-34329130	HL-60	blood:	n/a
47	chr17:34308567-34308617	LNCaP	prostate:	n/a
48	chr17:34325375-34325425	SAEC	small airway:	n/a
49	chr17:34344995-34345045	T-47D	breast:	n/a
50	chr17:34345172-34345222	HEK293	kidney:	embryo

(count:21 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr17:34296176..34297342-chr17:34476096..34477335,5	MCF-7	breast:
2	chr17:34296213..34297122-chr17:34336462..34336967,2	K562	blood:
3	chr17:34303464..34306413-chr17:34309070..34311922,2	MCF-7	breast:
4	chr17:34311368..34313666-chr17:34316292..34318623,2	K562	blood:
5	chr17:34302946..34303533-chr17:34476286..34476890,2	MCF-7	breast:
6	chr17:34296279..34296828-chr17:34838515..34839445,2	MCF-7	breast:
7	chr17:34315914..34317851-chr17:34318503..34320854,2	K562	blood:
8	chr17:34339180..34340890-chr17:34344090..34346721,2	K562	blood:
9	chr17:34363677..34365239-chr17:34371843..34374735,2	K562	blood:
10	chr17:34339180..34340890-chr17:34344090..34346721,2	K562	blood:
11	chr17:34359094..34361696-chr17:34362624..34365203,2	K562	blood:
12	chr17:34298765..34300848-chr17:34316779..34319747,2	K562	blood:
13	chr17:34303464..34306413-chr17:34309070..34311922,2	MCF-7	breast:
14	chr17:34302700..34304055-chr17:34336077..34336605,4	K562	blood:
15	chr17:34274196..34274787-chr17:34302700..34303672,2	K562	blood:
16	chr17:34359094..34361696-chr17:34362624..34365203,2	K562	blood:
17	chr17:34298765..34300848-chr17:34316779..34319747,2	K562	blood:
18	chr17:34296429..34297161-chr17:34476008..34476598,8	K562	blood:
19	chr17:34309062..34309701-chr17:34476081..34477023,4	MCF-7	breast:
20	chr17:34315914..34317851-chr17:34318503..34320854,2	K562	blood:
21	chr17:34302767..34303445-chr17:34399612..34400175,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CCL15-1	chr17:34313607-34313740	NR_027922
2	lnc-CCL18-4	chr17:34339544-34339931	ENSG00000267431.1
3	lnc-CCL18-2	chr17:34313570-34317305	ENSG00000251502
4	lnc-CCL15-1	chr17:34324757-34324896	NR_027922
5	lnc-CCL15-1	chr17:34328456-34329084	NR_027921
6	lnc-CCL15-1	chr17:34311374-34311488	NR_027921
7	lnc-CCL15-1	chr17:34311374-34311488	NR_027922
8	lnc-CCL15-1	chr17:34310692-34310924	NR_027922
9	lnc-CCL23-1	chr17:34365072-34365175	XLOC_012449
10	lnc-CCL15-1	chr17:34324757-34324896	NR_027921
11	lnc-CCL15-1	chr17:34313607-34313740	NR_027921
12	lnc-CCL18-5	chr17:34337060-34337452	ENSG00000267566.1
13	lnc-CCL15-1	chr17:34325902-34325961	NR_027921
14	lnc-CCL15-1	chr17:34325902-34325961	NR_027922
15	lnc-CCL15-1	chr17:34312784-34312831	NR_027921
16	lnc-CCL15-1	chr17:34325316-34325427	NR_027921
17	lnc-CCL18-5	chr17:34337060-34338658	ENSG00000267566.1
18	lnc-CCL18-5	chr17:34328458-34328656	ENSG00000267566.1
19	lnc-CCL15-1	chr17:34328456-34329084	NR_027922
20	lnc-CCL15-1	chr17:34310692-34310924	NR_027921
21	lnc-CCL15-1	chr17:34325316-34325427	NR_027922
22	lnc-CCL18-5	chr17:34336602-34336723	ENSG00000267566.1
23	lnc-CCL18-2	chr17:34312626-34312761	ENSG00000251502

No data

Variant related genes	Relation type
ENSG00000267657	TF binding region
ENSG00000267431	TF binding region
CCL15	TF binding region
CCL23	TF binding region
ENSG00000266956	TF binding region
CCL16	TF binding region
ENSG00000267566	TF binding region
CCL15-CCL14	TF binding region
CCL14	TF binding region
ENSG00000267657	CpG island
ENSG00000267431	CpG island
CCL15	CpG island
CCL23	CpG island
ENSG00000266956	CpG island
CCL16	CpG island
ENSG00000267566	CpG island
CCL15-CCL14	CpG island
CCL14	CpG island
ENSG00000266956	chromatin interactions
ENSG00000161573	chromatin interactions
ENSG00000267566	chromatin interactions
ENSG00000167236	chromatin interactions
ENSG00000267431	chromatin interactions
AEBP2	miRNA target sites
TLE4	miRNA target sites

Extended variants
information (count: 3292 )
Associated
traits (count: 125 )

Variant overlapped rSNPs/rCNVs (count:3292 , 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	rs550914526	chr17:34285326-34285327	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs187272013	chr17:34285351-34285352	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs377509270	chr17:34285365-34285366	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs545524994	chr17:34285377-34285378	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs4796143	chr17:34285393-34285394	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
6	rs550622956	chr17:34285413-34285414	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs567580917	chr17:34285438-34285439	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs1719188	chr17:34285479-34285480	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs534049692	chr17:34285517-34285518	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs536436119	chr17:34285648-34285649	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs553246911	chr17:34285701-34285702	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs553687195	chr17:34285729-34285730	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs370652449	chr17:34285754-34285755	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs34342884	chr17:34285789-34285790	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs373761310	chr17:34285814-34285815	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs572571638	chr17:34285825-34285826	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs112685903	chr17:34285830-34285831	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs145114545	chr17:34285835-34285836	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs60040586	chr17:34285848-34285849	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs190777933	chr17:34285882-34285883	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs374524597	chr17:34285998-34285999	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs181810549	chr17:34286004-34286005	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs1734975	chr17:34286028-34286029	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs115458902	chr17:34286052-34286053	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs1734974	chr17:34286101-34286102	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs371802642	chr17:34286102-34286103	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs1734973	chr17:34286104-34286105	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs186050759	chr17:34286115-34286116	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs551076240	chr17:34286133-34286134	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs1719183	chr17:34286174-34286175	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs558606398	chr17:34286227-34286228	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs530403363	chr17:34286257-34286258	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs150320000	chr17:34286308-34286309	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs201090411	chr17:34286378-34286379	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs377599521	chr17:34286380-34286381	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs62078063	chr17:34286452-34286453	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs190472846	chr17:34286469-34286470	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs182570462	chr17:34286494-34286495	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs546772445	chr17:34286496-34286497	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs149118977	chr17:34286504-34286505	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs1617347	chr17:34286521-34286522	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs557947316	chr17:34286543-34286544	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs578071914	chr17:34286554-34286555	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs537039899	chr17:34286564-34286565	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs557370190	chr17:34286576-34286577	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs185288946	chr17:34286600-34286601	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs73286983	chr17:34286619-34286620	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs559486109	chr17:34286740-34286741	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs2526333	chr17:34286745-34286746	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs545612022	chr17:34286749-34286750	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:125)

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
Breast cancer	21364760	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Adrenocortical carcinoma	18281524	CNVD
Lung cancer	21569311	CNVD
Gastric cancer	21811585	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	16620391	CNVD
Prostate cancer	18632612	CNVD
Acute myeloid leukemia	20824076	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Breast cancer	21509527	CNVD
Cancer	17440070	CNVD
early-passage human iPS cells	21368824	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:549 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr17:34275000-34296600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
2	chr17:34295600-34302200	Enhancers	Liver	Liver
3	chr17:34295800-34299600	Enhancers	HepG2	liver
4	chr17:34296400-34297200	Enhancers	Fetal Kidney	kidney
5	chr17:34296600-34296800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr17:34296600-34297000	Enhancers	Primary T helper naive cells from peripheral blood	blood
7	chr17:34296600-34297200	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
8	chr17:34296600-34297400	Enhancers	Primary T cells fromperipheralblood	blood
9	chr17:34296600-34299800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
10	chr17:34296800-34297000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
11	chr17:34296800-34297000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
12	chr17:34296800-34297000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
13	chr17:34296800-34297000	Enhancers	Lung	lung
14	chr17:34296800-34297000	Enhancers	Right Atrium	heart
15	chr17:34296800-34297000	Enhancers	Sigmoid Colon	Sigmoid Colon
16	chr17:34296800-34297000	Enhancers	Spleen	Spleen
17	chr17:34296800-34297000	Enhancers	HUVEC	blood vessel
18	chr17:34296800-34297200	Enhancers	ES-I3 Cell Line	embryonic stem cell
19	chr17:34296800-34297200	Flanking Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
20	chr17:34296800-34297200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
21	chr17:34296800-34297200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
22	chr17:34296800-34297200	Enhancers	Adipose Nuclei	Adipose
23	chr17:34296800-34297200	Enhancers	Pancreas	Pancrea
24	chr17:34296800-34297200	Enhancers	Rectal Mucosa Donor 29	rectum
25	chr17:34296800-34297200	Enhancers	Rectal Mucosa Donor 31	rectum
26	chr17:34296800-34297200	Enhancers	Skeletal Muscle Male	skeletal muscle
27	chr17:34296800-34297400	Enhancers	iPS-15b Cell Line	embryonic stem cell
28	chr17:34296800-34297400	Enhancers	Duodenum Mucosa	Duodenum
29	chr17:34296800-34299400	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
30	chr17:34296800-34302800	Enhancers	Fetal Intestine Large	intestine
31	chr17:34296800-34303400	Enhancers	Fetal Intestine Small	intestine
32	chr17:34297000-34297200	Enhancers	Skeletal Muscle Female	skeletal muscle
33	chr17:34297000-34297200	Enhancers	Small Intestine	intestine
34	chr17:34297000-34298400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
35	chr17:34297000-34298400	Weak transcription	HUVEC	blood vessel
36	chr17:34297000-34299600	Weak transcription	Lung	lung
37	chr17:34297000-34300600	Weak transcription	Right Atrium	heart
38	chr17:34297000-34302600	Weak transcription	Spleen	Spleen
39	chr17:34297000-34316600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
40	chr17:34297200-34298400	Weak transcription	Adipose Nuclei	Adipose
41	chr17:34297200-34299600	Weak transcription	Sigmoid Colon	Sigmoid Colon
42	chr17:34297200-34299600	Weak transcription	Skeletal Muscle Male	skeletal muscle
43	chr17:34297200-34299800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
44	chr17:34297200-34299800	Weak transcription	Rectal Mucosa Donor 31	rectum
45	chr17:34297200-34300000	Weak transcription	Rectal Mucosa Donor 29	rectum
46	chr17:34297200-34300000	Weak transcription	Small Intestine	intestine
47	chr17:34297200-34300400	Weak transcription	Pancreas	Pancrea
48	chr17:34297200-34302600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
49	chr17:34297400-34297800	Weak transcription	Duodenum Mucosa	Duodenum
50	chr17:34297400-34299600	Weak transcription	Skeletal Muscle Female	skeletal muscle

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