Variant report

Variant	nsv1061489
Chromosome Location	chr17:19654704-19705026
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1354)
CpG islands
(count:183)
Chromatin interactive
region (count:52)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1354 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr17:19669870-19670061	HepG2	liver:	n/a	n/a
2	ARID3A	chr17:19684890-19685276	HepG2	liver:	n/a	n/a
3	ARID3A	chr17:19665881-19666126	HepG2	liver:	n/a	n/a
4	ATF2	chr17:19658022-19658493	GM12878	blood:	n/a	n/a
5	ATF3	chr17:19656201-19656926	A549	lung:	n/a	n/a
6	ATF3	chr17:19657083-19657608	A549	lung:	n/a	n/a
7	ATF3	chr17:19669755-19670183	H1-hESC	embryonic stem cell:	n/a	chr17:19669960-19669969
8	ATF3	chr17:19655686-19657537	A549	lung:	n/a	n/a
9	BACH1	chr17:19682268-19682386	H1-hESC	embryonic stem cell:	n/a	n/a
10	BACH1	chr17:19657204-19657396	H1-hESC	embryonic stem cell:	n/a	n/a
11	BACH1	chr17:19656327-19656687	H1-hESC	embryonic stem cell:	n/a	n/a
12	BATF	chr17:19659137-19659427	GM12878	blood:	n/a	n/a
13	BCL11A	chr17:19659127-19659464	GM12878	blood:	n/a	n/a
14	BCL11A	chr17:19658028-19658373	GM12878	blood:	n/a	n/a
15	BCL3	chr17:19659031-19659510	GM12878	blood:	n/a	n/a
16	BCL3	chr17:19655518-19657605	A549	lung:	n/a	n/a
17	BCL3	chr17:19669652-19670266	A549	lung:	n/a	n/a
18	BCL3	chr17:19655354-19657717	A549	lung:	n/a	n/a
19	BCLAF1	chr17:19669814-19670148	GM12878	blood:	n/a	n/a
20	BHLHE40	chr17:19655484-19656735	A549	lung:	n/a	n/a
21	BHLHE40	chr17:19669850-19670095	K562	blood:	n/a	chr17:19670009-19670025
22	BRCA1	chr17:19656321-19657468	Hela-S3	cervix:	n/a	n/a
23	BRCA1	chr17:19669791-19670002	HepG2	liver:	n/a	n/a
24	CBX3	chr17:19699803-19700104	K562	blood:	n/a	n/a
25	CEBPB	chr17:19655194-19655497	ECC-1	luminal epithelium:	n/a	n/a
26	CEBPB	chr17:19673348-19673677	IMR90	lung:	n/a	n/a
27	CEBPB	chr17:19684843-19685211	HepG2	liver:	n/a	chr17:19685026-19685037 chr17:19685024-19685035
28	CEBPB	chr17:19656310-19656824	ECC-1	luminal epithelium:	n/a	n/a
29	CEBPB	chr17:19678003-19678209	A549	lung:	n/a	chr17:19678118-19678129
30	CEBPB	chr17:19655093-19655469	Hela-S3	cervix:	n/a	n/a
31	CEBPB	chr17:19684871-19685082	A549	lung:	n/a	chr17:19685026-19685037 chr17:19685024-19685035
32	CEBPB	chr17:19655207-19655486	ECC-1	luminal epithelium:	n/a	n/a
33	CEBPB	chr17:19678081-19678242	HepG2	liver:	n/a	chr17:19678118-19678129
34	CEBPB	chr17:19684882-19685159	K562	blood:	n/a	chr17:19685026-19685037 chr17:19685024-19685035
35	CEBPB	chr17:19655106-19655389	A549	lung:	n/a	n/a
36	CEBPB	chr17:19684853-19685205	Hela-S3	cervix:	n/a	chr17:19685026-19685037 chr17:19685024-19685035
37	CEBPB	chr17:19655733-19657520	Hela-S3	cervix:	n/a	n/a
38	CEBPB	chr17:19688554-19688615	A549	lung:	n/a	n/a
39	CEBPB	chr17:19673407-19673617	Hela-S3	cervix:	n/a	n/a
40	CEBPB	chr17:19684806-19685210	MCF-7	breast:	n/a	chr17:19685026-19685037 chr17:19685024-19685035
41	CHD1	chr17:19665934-19666012	GM12878	blood:	n/a	n/a
42	CHD2	chr17:19669995-19670016	K562	blood:	n/a	n/a
43	CHD2	chr17:19656207-19657517	Hela-S3	cervix:	n/a	n/a
44	CHD2	chr17:19669804-19670143	Hela-S3	cervix:	n/a	n/a
45	CHD2	chr17:19669913-19670057	HepG2	liver:	n/a	n/a
46	CREB1	chr17:19656980-19657466	A549	lung:	n/a	n/a
47	CREB1	chr17:19655590-19656108	A549	lung:	n/a	n/a
48	CREB1	chr17:19665762-19666234	A549	lung:	n/a	n/a
49	CREB1	chr17:19669744-19670211	A549	lung:	n/a	n/a
50	CREB1	chr17:19656124-19656814	A549	lung:	n/a	n/a

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr17:19674148-19674198	PFSK-1	brain:	n/a
2	chr17:19675785-19675835	A549	lung:	n/a
3	chr17:19656554-19656604	Caco-2	colon:	n/a
4	chr17:19656554-19656604	SAEC	small airway:	n/a
5	chr17:19656554-19656604	HRE	kidney:	n/a
6	chr17:19675785-19675835	NT2-D1	testis:	n/a
7	chr17:19656554-19656604	BE2_C	brain:	n/a
8	chr17:19675785-19675835	GM19239	blood:	n/a
9	chr17:19674148-19674198	BE2_C	brain:	n/a
10	chr17:19656554-19656604	AG10803	skin:	n/a
11	chr17:19674148-19674198	GM12892	blood:	n/a
12	chr17:19656554-19656604	HL-60	blood:	n/a
13	chr17:19656554-19656604	A549	lung:	n/a
14	chr17:19674148-19674198	A549	lung:	n/a
15	chr17:19674148-19674198	GM06990	blood:	n/a
16	chr17:19656554-19656604	GM12878	blood:	n/a
17	chr17:19674148-19674198	HRE	kidney:	n/a
18	chr17:19656554-19656604	HCF	heart:	n/a
19	chr17:19675785-19675835	HAEpiC	amniotic membrane:	n/a
20	chr17:19674148-19674198	K562	blood:	n/a
21	chr17:19675785-19675835	MCF10A-Er-Src	breast:	n/a
22	chr17:19674148-19674198	HepG2	liver:	n/a
23	chr17:19675785-19675835	AG04450	lung:	fetal
24	chr17:19656554-19656604	GM06990	blood:	n/a
25	chr17:19675785-19675835	H1-hESC	embryonic stem cell:	embryo
26	chr17:19656554-19656604	ovcar-3	ovarian:	n/a
27	chr17:19674148-19674198	MCF-7	breast:	n/a
28	chr17:19656554-19656604	RPTEC	kidney:	n/a
29	chr17:19674148-19674198	HAEpiC	amniotic membrane:	n/a
30	chr17:19675785-19675835	Jurkat	blood:	n/a
31	chr17:19656554-19656604	PrEC	prostate:	n/a
32	chr17:19656554-19656604	PANC-1	pancreas:	n/a
33	chr17:19656554-19656604	SKMC	muscle:	n/a
34	chr17:19674148-19674198	HPAEpiC	pulmonary alveolar:	n/a
35	chr17:19656554-19656604	AG09309	skin:	n/a
36	chr17:19674148-19674198	NHBE	bronchial:	n/a
37	chr17:19674148-19674198	HCM	heart:	n/a
38	chr17:19675785-19675835	BJ	skin:	n/a
39	chr17:19656554-19656604	HIPEpiC	eye:	n/a
40	chr17:19656554-19656604	ECC-1	luminal epithelium:	n/a
41	chr17:19656554-19656604	SK-N-MC	brain:	n/a
42	chr17:19674148-19674198	ECC-1	luminal epithelium:	n/a
43	chr17:19675785-19675835	Hela-S3	cervix:	n/a
44	chr17:19674148-19674198	Hela-S3	cervix:	n/a
45	chr17:19674148-19674198	GM12878	blood:	n/a
46	chr17:19656554-19656604	HNPCEpiC	eye:	n/a
47	chr17:19656554-19656604	AG04449	skin:	fetal
48	chr17:19675785-19675835	HNPCEpiC	eye:	n/a
49	chr17:19675785-19675835	HUVEC	blood vessel:	n/a
50	chr17:19656554-19656604	NHBE	bronchial:	n/a

(count:52 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr17:19416908..19417958-chr17:19669541..19670560,5	K562	blood:
2	chr11:67397857..67399603-chr17:19654494..19656370,2	MCF-7	breast:
3	chr17:19264651..19266325-chr17:19665635..19668474,2	MCF-7	breast:
4	chr11:67397006..67400354-chr17:19655005..19658242,3	MCF-7	breast:
5	chr11:67407271..67408048-chr17:19655503..19656398,3	MCF-7	breast:
6	chr17:19449914..19450512-chr17:19669552..19670133,2	MCF-7	breast:
7	chr17:19417328..19417882-chr17:19669379..19670090,2	MCF-7	breast:
8	chr11:67382088..67384067-chr17:19655991..19658673,2	MCF-7	breast:
9	chr17:19649191..19653636-chr17:19654131..19659903,8	MCF-7	breast:
10	chr17:19665481..19667354-chr17:19668063..19669957,3	MCF-7	breast:
11	chr17:19700984..19703943-chr17:19714098..19715864,2	MCF-7	breast:
12	chr17:19416820..19417560-chr17:19665539..19666441,2	MCF-7	breast:
13	chr17:19657020..19657638-chr17:19669487..19670405,2	MCF-7	breast:
14	chr17:19656623..19657451-chr17:19665588..19666274,2	MCF-7	breast:
15	chr11:67380849..67383590-chr17:19654631..19658826,3	MCF-7	breast:
16	chr17:19414307..19417515-chr17:19668492..19670965,3	MCF-7	breast:
17	chr17:19676715..19677229-chr17:19913049..19913859,2	MCF-7	breast:
18	chr11:67398077..67399002-chr17:19665643..19666146,2	MCF-7	breast:
19	chr17:19679774..19681757-chr17:19685256..19686882,2	MCF-7	breast:
20	chr17:19627605..19629507-chr17:19658894..19661026,2	MCF-7	breast:
21	chr17:19647019..19648897-chr17:19661200..19664189,2	MCF-7	breast:
22	chr11:67139722..67141643-chr17:19656038..19657945,2	MCF-7	breast:
23	chr11:67396737..67399523-chr17:19660165..19662735,2	MCF-7	breast:
24	chr17:19656684..19658708-chr17:19659226..19661401,3	MCF-7	breast:
25	chr11:67405096..67409176-chr17:19654881..19658832,8	MCF-7	breast:
26	chr17:19662944..19666237-chr17:19667873..19670439,4	MCF-7	breast:
27	chr11:67395858..67398649-chr17:19668230..19671876,3	MCF-7	breast:
28	chr17:19685995..19688527-chr17:19689304..19691590,2	K562	blood:
29	chr17:19654497..19661140-chr17:19661473..19671609,12	MCF-7	breast:
30	chr17:19657133..19657845-chr20:45802558..45803277,2	MCF-7	breast:
31	chr11:67149008..67150613-chr17:19656460..19658061,2	MCF-7	breast:
32	chr11:67396418..67397288-chr17:19669617..19670437,3	MCF-7	breast:
33	chr17:19264857..19267680-chr17:19664329..19666250,2	K562	blood:
34	chr17:19669950..19670557-chr17:19681270..19681904,2	K562	blood:
35	chr17:19656623..19657451-chr17:19665588..19666274,2	MCF-7	breast:
36	chr17:19678434..19679096-chr3:131689247..131689840,2	MCF-7	breast:
37	chr11:67396022..67398380-chr17:19664074..19665583,2	MCF-7	breast:
38	chr17:19657020..19657638-chr17:19669487..19670405,2	MCF-7	breast:
39	chr11:67406449..67409216-chr17:19654457..19656822,7	MCF-7	breast:
40	chr17:19622195..19622792-chr17:19656909..19657524,3	MCF-7	breast:
41	chr17:19697847..19700203-chr17:19701124..19704038,2	K562	blood:
42	chr11:67397884..67398710-chr17:19656962..19657673,2	MCF-7	breast:
43	chr17:19665481..19667354-chr17:19668063..19669957,3	MCF-7	breast:
44	chr17:19641453..19644108-chr17:19654195..19656369,2	MCF-7	breast:
45	chr17:19688891..19689853-chr17:20019794..20020671,3	MCF-7	breast:
46	chr17:19669950..19670557-chr17:19681270..19681904,2	K562	blood:
47	chr17:19662944..19666237-chr17:19667873..19670439,4	MCF-7	breast:
48	chr17:19688998..19689701-chr17:19715846..19716392,2	MCF-7	breast:
49	chr17:19621105..19622742-chr17:19656130..19658211,2	MCF-7	breast:
50	chr11:67397793..67398676-chr17:19669612..19670394,2	MCF-7	breast:

(count:3 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ULK2-3	chr17:19673034-19673078	NONHSAT146526
2	lnc-ULK2-2	chr17:19674142-19677237	NONHSAT146527
3	lnc-ULK2-3	chr17:19669462-19669834	NONHSAT146526

No data

Variant related genes	Relation type
ENSG00000230607	TF binding region
ULK2	TF binding region
ALDH3A1	TF binding region
ENSG00000230607	CpG island
ULK2	CpG island
ALDH3A1	CpG island
ENSG00000083290	chromatin interactions
ENSG00000128487	chromatin interactions
ENSG00000175505	chromatin interactions
ENSG00000262681	chromatin interactions
ENSG00000231793	chromatin interactions
ENSG00000256514	chromatin interactions
ENSG00000167799	chromatin interactions
ENSG00000108602	chromatin interactions
ENSG00000180638	chromatin interactions
ENSG00000167800	chromatin interactions
ENSG00000230607	chromatin interactions
ENSG00000108641	chromatin interactions

Extended variants
information (count: 2052 )
Associated
traits (count: 157 )

Variant overlapped rSNPs/rCNVs (count:2052 , 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	rs540066535	chr17:19654796-19654797	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
2	rs77278457	chr17:19654797-19654798	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
3	rs76591829	chr17:19654798-19654799	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
4	rs76431136	chr17:19654799-19654800	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
5	rs182338495	chr17:19654817-19654818	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
6	rs529005054	chr17:19654818-19654819	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
7	rs548552116	chr17:19654819-19654820	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
8	rs115556068	chr17:19654855-19654856	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
9	rs557120328	chr17:19654859-19654860	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
10	rs141359480	chr17:19654887-19654888	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
11	rs569608101	chr17:19654908-19654909	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
12	rs187467445	chr17:19654928-19654929	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
13	rs377454152	chr17:19654945-19654946	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
14	rs540154459	chr17:19654959-19654960	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
15	rs546924647	chr17:19654972-19654973	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs566936833	chr17:19654997-19654998	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
17	rs193256847	chr17:19655001-19655002	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
18	rs555914347	chr17:19655068-19655069	Weak transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
19	rs143756200	chr17:19655077-19655078	Weak transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
20	rs538248535	chr17:19655089-19655090	Weak transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
21	rs183741379	chr17:19655123-19655124	Weak transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
22	rs577903161	chr17:19655146-19655147	Weak transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
23	rs540397349	chr17:19655165-19655166	Weak transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
24	rs553715881	chr17:19655179-19655180	Weak transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
25	rs553105151	chr17:19655245-19655246	Weak transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
26	rs78963582	chr17:19655305-19655306	Weak transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
27	rs374665637	chr17:19655308-19655309	Weak transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
28	rs398041582	chr17:19655326-19655327	Weak transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
29	rs60679113	chr17:19655327-19655328	Weak transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
30	rs374968958	chr17:19655338-19655339	Weak transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
31	rs542285270	chr17:19655339-19655340	Weak transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
32	rs562245196	chr17:19655345-19655346	Weak transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
33	rs76509440	chr17:19655375-19655376	Weak transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
34	rs544645152	chr17:19655382-19655383	Weak transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
35	rs564797926	chr17:19655394-19655395	Weak transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
36	rs561595234	chr17:19655398-19655399	Weak transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
37	rs533485418	chr17:19655445-19655446	Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
38	rs547156263	chr17:19655447-19655448	Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
39	rs201418379	chr17:19655448-19655449	Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
40	rs566917834	chr17:19655467-19655468	Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
41	rs75275533	chr17:19655475-19655476	Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
42	rs529533652	chr17:19655486-19655487	Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
43	rs188731909	chr17:19655532-19655533	Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
44	rs558463666	chr17:19655535-19655536	Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
45	rs569385716	chr17:19655587-19655588	Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
46	rs538236339	chr17:19655616-19655617	Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
47	rs558233533	chr17:19655619-19655620	Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
48	rs571500782	chr17:19655696-19655697	Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
49	rs369039229	chr17:19655706-19655707	Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
50	rs533808616	chr17:19655707-19655708	Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:157)

Disease	PMID	Source
Burkitt''s lymphoma	19759907	CNVD
Wilms tumour	21544195	CNVD
Esophageal adenocarcinoma	18519675	CNVD
lymphocytic leukemia	21291569	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Melanoma	18172304	CNVD
Medulloblastoma	21979893	CNVD
Breast cancer	16608533	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Chordoma	21602918	CNVD
Miller-Dieker syndrome	22283845	CNVD
Non-syndromic sensorineural hearing loss	17457615	CNVD
Cancer	22429812	CNVD
Chronic lymphocytic leukemia	21795749	CNVD
Ewing''s sarcoma	21437220	CNVD
Follicular lymphoma	19010834	CNVD
Colorectal cancer	20709793	CNVD
Acute myeloid leukemia	16864856	CNVD
Endometrial cancer	22040021	CNVD
Paraganglioma	21461997	CNVD
Pheochromocytoma	21461997	CNVD
Breast cancer	22028636	CNVD
Breast cancer	20837533	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Hepatocellular carcinoma	22174799	CNVD
Medulloblastoma	21292688	CNVD
colon cancer	17210682	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Basal cell lymphoma	17053054	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Cancer	16751803	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Colorectal cancer	19359472	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Chronic lymphocytic leukemia	17971485	CNVD
Basal cell lymphoma	17170743	CNVD
Breast cancer	16461572	CNVD
Colorectal cancer	16272173	CNVD
Follicular lymphoma	17170743	CNVD
Human rectal carcinomas	16397240	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Breast cancer	17133270	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
Ovarian cancer	22174824	CNVD
Moyamoya disease	22323933	CNVD
small cell lung cancer	20016488	CNVD
Acute myeloid leukemia	20729466	CNVD
Acute promyelocytic leukemia	19109227	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Urothelial carcinoma	21177765	CNVD
Acute myeloid leukemia	21251322	CNVD
Myelodysplastic syndrome	21251322	CNVD
Cancer	20164919	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Acute myeloid leukemia	20724749	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
Acute myeloid leukemia	17237825	CNVD
Colorectal cancer	21645411	CNVD
HIV/AIDS	22844521	CNVD
Psoriasis	22844521	CNVD
Rheumatoid arthritis	22844521	CNVD
Sclerosis systemic	22844521	CNVD
Systemic lupus erythematosus	22844521	CNVD
HIV/AIDS	17953491	CNVD
HIV/AIDS	20877625	CNVD
Immune disease	21076436	CNVD
Rheumatoid arthritis	17953491	CNVD
Type 1 diabetes	17953491	CNVD
HIV/AIDS	15637236	CNVD
Prostate cancer	18632612	CNVD
Lung cancer	18438408	CNVD
Ovarian cancer	21781307	CNVD
Autism	22495311	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Neurofibromatosis	18196300	CNVD
Colorectal cancer	16774939	CNVD
Breast cancer	17001317	CNVD
Rhabdomyosarcoma	16790082	CNVD
Charcot-marie-tooth disease	16463004	CNVD
Osteosarcoma	22292074	CNVD
Breast cancer	17603634	CNVD
Charcot	16760730	CNVD
Mental retardation	17901693	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
ovarian endometriomas	16273235	CNVD
Smith-Magenis syndrome	18923513	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	16272173	CNVD
Austim spectrum disorder	21302340	CNVD
Autism	22492990	CNVD
Congenital abnormalities	21549014	CNVD
Developmental delay	18414209	CNVD
Developmental delay	21549014	CNVD
Epilepsy	20970697	CNVD
Mental retardation	18414209	CNVD
Mental retardation	21549014	CNVD
Smith-Magenis syndrome	21981782	CNVD
Smith-Magenis syndrome	20188345	CNVD
Smith-Magenis syndrome	16775514	CNVD
Smith-Magenis syndrome	22585170	CNVD
Smith-Magenis syndrome	22241247	CNVD
Autism	20970697	CNVD
Mental retardation	19951919	CNVD
Potocki-Lupski syndrome	21271655	CNVD
Potocki-lupski syndrome	17357070	CNVD
Potocki-lupski syndrome	20110824	CNVD
Potocki-lupski syndrome	18923514	CNVD
Potocki-lupski syndrome	22241247	CNVD
Potocki-lupski syndrome	20188345	CNVD
Schizophrenia	21399695	CNVD
Mental retardation	16773131	CNVD
Adenocarcinoma	19607727	CNVD
Squamous cell cancer	19607727	CNVD
Non-small cell lung cancer	21829676	CNVD
Glioblastoma multiforme	17002787	CNVD
Charcot-marie-tooth disease	22470819	CNVD
Neurofibromatosis	22470819	CNVD
Neuropathy	22470819	CNVD
Smith-Magenis syndrome	18301319	CNVD
Smith-Magenis syndrome	17357070	CNVD
Smith-Magenis syndrome	18469339	CNVD
Smith-Magenis syndrome	22241097	CNVD
Smith-Magenis syndrome	22470819	CNVD
Tourette syndrome	18923514	CNVD
Type 1 diabetes	22470819	CNVD
Potocki-lupski syndrome	18469339	CNVD
Follicular lymphoma	20505157	CNVD
T-cell lymphomas	19863542	CNVD
Neuropathy	17597781	CNVD
Hepatocellular carcinoma	16750200	CNVD
Neurodevelopmental disorder	17015230	CNVD
Smith-Magenis syndrome	17597781	CNVD
Potocki-lupski syndrome	18059269	CNVD
Potocki-lupski syndrome	17597781	CNVD
Mental retardation	17847001	CNVD
Multiple myeloma	16616336	CNVD
Breast cancer	20409316	CNVD
Autism	22543975	CNVD
Sezary syndrome	18413736	CNVD
Cancer	20164920	CNVD
Lung adenocarcinoma	21935476	CNVD
Melanoma	20877625	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:1508 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr17:19648800-19656200	Weak transcription	Aorta	Aorta
2	chr17:19648800-19657000	Weak transcription	Spleen	Spleen
3	chr17:19649000-19656400	Weak transcription	Right Atrium	heart
4	chr17:19649200-19656200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
5	chr17:19650200-19656800	Enhancers	Breast Myoepithelial Primary Cells	Breast
6	chr17:19650600-19657000	Enhancers	HMEC	breast
7	chr17:19650600-19657600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
8	chr17:19651000-19656200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
9	chr17:19651600-19654800	Enhancers	Esophagus	oesophagus
10	chr17:19652000-19655400	Weak transcription	HSMMtube	muscle
11	chr17:19652000-19655800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
12	chr17:19652200-19655800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
13	chr17:19652200-19655800	Weak transcription	Brain Angular Gyrus	brain
14	chr17:19652200-19656000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
15	chr17:19652200-19656000	Weak transcription	Cortex derived primary cultured neurospheres	brain
16	chr17:19652200-19656000	Weak transcription	Osteobl	bone
17	chr17:19652400-19655400	Weak transcription	Muscle Satellite Cultured Cells	--
18	chr17:19652400-19655400	Weak transcription	Brain Substantia Nigra	brain
19	chr17:19652400-19655600	Weak transcription	Adipose Nuclei	Adipose
20	chr17:19652400-19655600	Weak transcription	Brain Inferior Temporal Lobe	brain
21	chr17:19652400-19655800	Weak transcription	Brain Anterior Caudate	brain
22	chr17:19652400-19655800	Weak transcription	Brain Cingulate Gyrus	brain
23	chr17:19652400-19655800	Weak transcription	Skeletal Muscle Female	skeletal muscle
24	chr17:19652400-19656200	Weak transcription	Rectal Mucosa Donor 29	rectum
25	chr17:19652400-19656400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
26	chr17:19652400-19656600	Weak transcription	Pancreas	Pancrea
27	chr17:19652600-19655400	Weak transcription	Duodenum Mucosa	Duodenum
28	chr17:19652600-19655400	Weak transcription	Stomach Smooth Muscle	stomach
29	chr17:19652600-19655400	Enhancers	Hela-S3	cervix
30	chr17:19652600-19655400	Weak transcription	NHDF-Ad	bronchial
31	chr17:19652600-19655600	Weak transcription	Brain Hippocampus Middle	brain
32	chr17:19652600-19655800	Weak transcription	Colonic Mucosa	Colon
33	chr17:19652600-19656000	Weak transcription	Rectal Mucosa Donor 31	rectum
34	chr17:19652600-19656200	Weak transcription	HUES6 Cell Line	embryonic stem cell
35	chr17:19652600-19656600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
36	chr17:19652800-19654800	Enhancers	GM12878-XiMat	blood
37	chr17:19653400-19655400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
38	chr17:19653400-19657400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
39	chr17:19654200-19654800	Enhancers	Gastric	stomach
40	chr17:19654200-19654800	Enhancers	HSMM	muscle
41	chr17:19654200-19655000	Enhancers	HUVEC	blood vessel
42	chr17:19654400-19654800	Enhancers	HepG2	liver
43	chr17:19654400-19655800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
44	chr17:19654400-19658600	Enhancers	Stomach Mucosa	stomach
45	chr17:19654600-19654800	Flanking Active TSS	A549	lung
46	chr17:19654600-19654800	Enhancers	NHEK	skin
47	chr17:19654600-19655800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
48	chr17:19654600-19656000	Weak transcription	Sigmoid Colon	Sigmoid Colon
49	chr17:19654600-19656400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
50	chr17:19654600-19656400	Weak transcription	Lung	lung

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