Variant report

Variant	nsv878176
Chromosome Location	chr3:195926234-195959924
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:858)
CpG islands
(count:2014)
Chromatin interactive
region (count:47)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:858 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr3:195954641-195954826	HepG2	liver:	n/a	n/a
2	ARID3A	chr3:195941873-195942167	HepG2	liver:	n/a	n/a
3	ATF2	chr3:195959200-195959859	GM12878	blood:	n/a	n/a
4	ATF2	chr3:195959357-195959732	GM12878	blood:	n/a	n/a
5	ATF3	chr3:195935158-195935369	K562	blood:	n/a	n/a
6	ATF3	chr3:195934713-195934988	K562	blood:	n/a	n/a
7	BACH1	chr3:195933888-195934343	H1-hESC	embryonic stem cell:	n/a	n/a
8	BATF	chr3:195959765-195960161	GM12878	blood:	n/a	n/a
9	BATF	chr3:195959356-195959721	GM12878	blood:	n/a	n/a
10	BCL3	chr3:195946516-195946940	GM12878	blood:	n/a	n/a
11	BHLHE40	chr3:195941773-195942762	HepG2	liver:	n/a	chr3:195941846-195941862
12	BHLHE40	chr3:195929562-195929642	K562	blood:	n/a	n/a
13	BHLHE40	chr3:195935191-195935424	K562	blood:	n/a	n/a
14	BHLHE40	chr3:195946147-195946748	GM12878	blood:	n/a	n/a
15	BRCA1	chr3:195959266-195959342	GM12878	blood:	n/a	n/a
16	BRCA1	chr3:195929588-195929631	HepG2	liver:	n/a	n/a
17	BRCA1	chr3:195954649-195954670	HepG2	liver:	n/a	n/a
18	CBX3	chr3:195931986-195932441	HCT-116	colon:	n/a	n/a
19	CBX3	chr3:195934028-195934433	K562	blood:	n/a	n/a
20	CBX3	chr3:195935061-195935503	K562	blood:	n/a	n/a
21	CCNT2	chr3:195935230-195935267	K562	blood:	n/a	n/a
22	CEBPB	chr3:195946212-195946790	IMR90	lung:	n/a	n/a
23	CEBPB	chr3:195956005-195956141	K562	blood:	n/a	n/a
24	CEBPB	chr3:195929441-195929618	HepG2	liver:	n/a	n/a
25	CEBPB	chr3:195946582-195946893	HepG2	liver:	n/a	n/a
26	CEBPB	chr3:195932283-195933051	Hela-S3	cervix:	n/a	chr3:195932506-195932517
27	CEBPB	chr3:195932443-195932935	A549	lung:	n/a	chr3:195932506-195932517
28	CEBPB	chr3:195935358-195935438	HepG2	liver:	n/a	n/a
29	CEBPB	chr3:195947840-195948176	ECC-1	luminal epithelium:	n/a	n/a
30	CEBPB	chr3:195929388-195929727	HepG2	liver:	n/a	n/a
31	CEBPB	chr3:195926379-195926429	Hela-S3	cervix:	n/a	n/a
32	CEBPB	chr3:195941856-195942090	HepG2	liver:	n/a	n/a
33	CEBPB	chr3:195932341-195932660	K562	blood:	n/a	chr3:195932506-195932517
34	CEBPB	chr3:195932828-195933027	IMR90	lung:	n/a	n/a
35	CEBPB	chr3:195932341-195932923	HepG2	liver:	n/a	chr3:195932506-195932517
36	CEBPB	chr3:195936866-195937089	K562	blood:	n/a	n/a
37	CEBPD	chr3:195941700-195942049	HepG2	liver:	n/a	n/a
38	CHD1	chr3:195946518-195946606	GM12878	blood:	n/a	n/a
39	CHD2	chr3:195935517-195935584	HepG2	liver:	n/a	n/a
40	CHD2	chr3:195954612-195954656	HepG2	liver:	n/a	n/a
41	CHD2	chr3:195946790-195946792	HepG2	liver:	n/a	n/a
42	CHD2	chr3:195946307-195946566	GM12878	blood:	n/a	n/a
43	CHD2	chr3:195935307-195935343	K562	blood:	n/a	n/a
44	CHD2	chr3:195941889-195942059	HepG2	liver:	n/a	n/a
45	CTCF	chr3:195946380-195946530	BJ	skin:	n/a	n/a
46	CTCF	chr3:195926400-195926550	SK-N-SH_RA	brain:	n/a	n/a
47	CTCF	chr3:195934259-195934397	K562	blood:	n/a	n/a
48	CTCF	chr3:195926247-195926568	SK-N-SH	brain:	n/a	n/a
49	CTCF	chr3:195946420-195946570	GM12873	blood:	n/a	n/a
50	CTCF	chr3:195934191-195934468	K562	blood:	n/a	n/a

(count:2014 , 50 per page) page: 1 2 3 4 5 6 7 ... 41

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:195938668-195938718	HAEpiC	amniotic membrane:	n/a
2	chr3:195938668-195938718	HAEpiC	amniotic membrane:	n/a
3	chr3:195929492-195929542	HCM	heart:	n/a
4	chr3:195938436-195938486	AG09319	gingival:	n/a
5	chr3:195938048-195938098	HCM	heart:	n/a
6	chr3:195929544-195929594	AG09309	skin:	n/a
7	chr3:195943198-195943248	ProgFib	skin:	n/a
8	chr3:195943366-195943416	GM06990	blood:	n/a
9	chr3:195938436-195938486	BJ	skin:	n/a
10	chr3:195934604-195934654	HL-60	blood:	n/a
11	chr3:195934057-195934107	GM19239	blood:	n/a
12	chr3:195934355-195934405	AG04450	lung:	fetal
13	chr3:195954098-195954148	T-47D	breast:	n/a
14	chr3:195943713-195943763	AG04449	skin:	fetal
15	chr3:195942717-195942767	U87	brain:	n/a
16	chr3:195938048-195938098	HRPEpiC	eye:	n/a
17	chr3:195938668-195938718	GM12878	blood:	n/a
18	chr3:195940856-195940906	PFSK-1	brain:	n/a
19	chr3:195929544-195929594	GM12878	blood:	n/a
20	chr3:195943444-195943494	PFSK-1	brain:	n/a
21	chr3:195939310-195939360	AG10803	skin:	n/a
22	chr3:195934213-195934263	AG04449	skin:	fetal
23	chr3:195934411-195934461	MCF10A-Er-Src	breast:	n/a
24	chr3:195943366-195943416	U87	brain:	n/a
25	chr3:195929389-195929439	NH-A	brain:	n/a
26	chr3:195930486-195930536	GM12891	blood:	n/a
27	chr3:195934411-195934461	AG04450	lung:	fetal
28	chr3:195943366-195943416	AG09309	skin:	n/a
29	chr3:195939612-195939662	HIPEpiC	eye:	n/a
30	chr3:195929544-195929594	NHDF-neo	bronchial:	n/a
31	chr3:195939612-195939662	U87	brain:	n/a
32	chr3:195934350-195934400	HRE	kidney:	n/a
33	chr3:195946851-195946901	HEEpiC	esophagus:	n/a
34	chr3:195947062-195947112	HAEpiC	amniotic membrane:	n/a
35	chr3:195929389-195929439	Jurkat	blood:	n/a
36	chr3:195929544-195929594	PFSK-1	brain:	n/a
37	chr3:195938436-195938486	T-47D	breast:	n/a
38	chr3:195929389-195929439	AoSMC	blood vessel:	n/a
39	chr3:195943149-195943199	HEEpiC	esophagus:	n/a
40	chr3:195929492-195929542	A549	lung:	n/a
41	chr3:195939310-195939360	HUVEC	blood vessel:	n/a
42	chr3:195947062-195947112	SK-N-SH_RA	brain:	n/a
43	chr3:195929544-195929594	MCF10A-Er-Src	breast:	n/a
44	chr3:195940674-195940724	HCT-116	colon:	n/a
45	chr3:195943636-195943686	ovcar-3	ovarian:	n/a
46	chr3:195954098-195954148	GM19239	blood:	n/a
47	chr3:195943713-195943763	ECC-1	luminal epithelium:	n/a
48	chr3:195947062-195947112	SAEC	small airway:	n/a
49	chr3:195943444-195943494	HMEC	breast:	n/a
50	chr3:195939612-195939662	AG09309	skin:	n/a

(count:47 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:121484245..121485425-chr3:195957373..195958374,3	MCF-7	breast:
2	chr3:195952367..195954245-chr3:195957237..195960071,2	K562	blood:
3	chr3:195804970..195807492-chr3:195930599..195932477,2	K562	blood:
4	chr3:195921230..195923242-chr3:195932657..195935379,3	K562	blood:
5	chr3:195931871..195932800-chr3:196246135..196246657,2	K562	blood:
6	chr3:195786462..195788147-chr3:195930755..195932479,2	K562	blood:
7	chr3:195941305..195943379-chr3:195955106..195957288,2	K562	blood:
8	chr3:195793504..195812987-chr3:195901613..195938073,113	K562	blood:
9	chr1:121484917..121485731-chr3:195957374..195958374,2	MCF-7	breast:
10	chr3:195951103..195953764-chr3:195954363..195955891,2	K562	blood:
11	chr3:195819342..195820879-chr3:195934319..195935878,2	MCF-7	breast:
12	chr3:195942995..195944795-chr3:195945273..195947923,2	MCF-7	breast:
13	chr3:195945138..195947988-chr3:195949670..195951213,2	MCF-7	breast:
14	chr3:195770109..195772936-chr3:195923383..195926412,3	K562	blood:
15	chr3:195934199..195936662-chr3:196249592..196251250,2	K562	blood:
16	chr3:195807479..195809245-chr3:195949684..195952002,2	MCF-7	breast:
17	chr3:195806834..195810300-chr3:195921968..195927592,7	MCF-7	breast:
18	chr3:195805990..195808883-chr3:195933159..195936246,3	K562	blood:
19	chr3:195933131..195935157-chr3:196159454..196161102,2	K562	blood:
20	chr3:195933308..195935063-chr3:196012646..196014729,2	K562	blood:
21	chr3:195952367..195954245-chr3:195957237..195960071,2	K562	blood:
22	chr3:195785800..195787817-chr3:195933272..195935251,2	K562	blood:
23	chr3:195935114..195937817-chr3:195940401..195943040,3	K562	blood:
24	chr3:195952863..195955052-chr3:195973498..195975966,2	K562	blood:
25	chr3:195933778..195935330-chr3:195950925..195952641,2	MCF-7	breast:
26	chr3:195941305..195943379-chr3:195955106..195957288,2	K562	blood:
27	chr3:195935861..195938211-chr3:196064110..196066388,2	K562	blood:
28	chr3:195951103..195953764-chr3:195954363..195955891,2	K562	blood:
29	chr3:195932805..195936731-chr3:195940753..195943412,3	MCF-7	breast:
30	chr3:195932381..195937980-chr3:195939061..195944688,8	K562	blood:
31	chr3:195796379..195810322-chr3:195910077..195926320,43	MCF-7	breast:
32	chr3:195807469..195810377-chr3:195942089..195944693,4	MCF-7	breast:
33	chr3:195933623..195937361-chr3:196062207..196065610,4	K562	blood:
34	chr3:195807633..195809874-chr3:195932027..195934415,2	MCF-7	breast:
35	chr3:195958884..195960424-chr3:195972113..195974415,2	K562	blood:
36	chr3:195871532..195873508-chr3:195933763..195935660,2	K562	blood:
37	chr3:195933778..195935330-chr3:195950925..195952641,2	MCF-7	breast:
38	chr3:195927182..195928702-chr3:196245885..196247775,2	K562	blood:
39	chr3:195928850..195930702-chr3:195933758..195935376,2	K562	blood:
40	chr3:195807839..195810116-chr3:195932911..195935811,2	MCF-7	breast:
41	chr3:195945138..195947988-chr3:195949670..195951213,2	MCF-7	breast:
42	chr3:195934241..195936316-chr3:196228788..196231012,3	K562	blood:
43	chr3:195935114..195937817-chr3:195940401..195943040,3	K562	blood:
44	chr3:195947010..195950626-chr3:195954155..195955751,3	K562	blood:
45	chr3:195943354..195945789-chr3:195947655..195950538,2	K562	blood:
46	chr3:195793504..195812415-chr3:195915832..195927942,46	K562	blood:
47	chr3:195957001..195958662-chr3:195962028..195964022,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AC069257.9.1-8	chr3:195929220-195929681	l_2563_chr3:195910484-195920505_testes

No data

Variant related genes	Relation type
ENSG00000222335	TF binding region
ZDHHC19	TF binding region
SLC51A	TF binding region
ENSG00000222335	CpG island
ZDHHC19	CpG island
SLC51A	CpG island
ENSG00000145107	chromatin interactions
ENSG00000072274	chromatin interactions
ENSG00000228413	chromatin interactions
ENSG00000163961	chromatin interactions
ENSG00000273331	chromatin interactions
ENSG00000163959	chromatin interactions
ENSG00000161217	chromatin interactions
ENSG00000222335	chromatin interactions
ENSG00000252174	chromatin interactions

Extended variants
information (count: 1755 )
Associated
traits (count: 83 )

Variant overlapped rSNPs/rCNVs (count:1755 , 50 per page) page: 1 2 3 4 5 6 7 ... 36

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs939892	chr3:195926234-195926235	Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs372223614	chr3:195926240-195926241	Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
3	rs370034193	chr3:195926248-195926249	Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
4	rs60526982	chr3:195926288-195926289	Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
5	rs187342536	chr3:195926293-195926294	Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
6	rs35763359	chr3:195926294-195926295	Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
7	rs201605481	chr3:195926303-195926304	Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
8	rs11925607	chr3:195926310-195926311	Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
9	rs117786667	chr3:195926311-195926312	Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
10	rs117197592	chr3:195926315-195926316	Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
11	rs576933272	chr3:195926317-195926318	Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
12	rs544200127	chr3:195926352-195926353	Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
13	rs372878044	chr3:195926378-195926379	Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
14	rs76934383	chr3:195926387-195926388	Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
15	rs529758025	chr3:195926448-195926449	Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
16	rs548205335	chr3:195926466-195926467	Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
17	rs560143452	chr3:195926482-195926483	Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
18	rs577054742	chr3:195926500-195926501	Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
19	rs527394741	chr3:195926527-195926528	Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
20	rs541026656	chr3:195926528-195926529	Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
21	rs570980565	chr3:195926536-195926537	Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
22	rs538414994	chr3:195926537-195926538	Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
23	rs550239197	chr3:195926545-195926546	Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
24	rs386670145	chr3:195926552-195926553	Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
25	rs146281017	chr3:195926554-195926555	Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
26	rs112899967	chr3:195926589-195926590	Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
27	rs574746029	chr3:195926610-195926611	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
28	rs139190629	chr3:195926612-195926613	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
29	rs149468329	chr3:195926614-195926615	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
30	rs563627266	chr3:195926620-195926621	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
31	rs530601499	chr3:195926635-195926636	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
32	rs576999650	chr3:195926636-195926637	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
33	rs544386861	chr3:195926637-195926638	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
34	rs192641223	chr3:195926640-195926641	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
35	rs556561701	chr3:195926643-195926644	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs184624865	chr3:195926644-195926645	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs190532269	chr3:195926673-195926674	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs11922691	chr3:195926677-195926678	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs34898770	chr3:195926680-195926681	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs564190981	chr3:195926683-195926684	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs548346552	chr3:195926684-195926685	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs7622459	chr3:195926685-195926686	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs568266057	chr3:195926686-195926687	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs372912420	chr3:195926688-195926689	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs547649623	chr3:195926689-195926690	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs565756388	chr3:195926693-195926694	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs113772451	chr3:195926695-195926696	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs570132514	chr3:195926696-195926697	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs537103446	chr3:195926704-195926705	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs550973393	chr3:195926708-195926709	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:83)

Disease	PMID	Source
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Glioblastoma multiforme	21080181	CNVD
Retinoblastoma	21504564	CNVD
Medulloblastoma	21979893	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
Squamous cell cancer	20885788	CNVD
Melanoma	18172304	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	16461572	CNVD
Neuroblastoma	17533364	CNVD
Cervical Cancer	21857958	CNVD
Melanoma	21693616	CNVD
Lung cancer	21426551	CNVD
Cancer	21637783	CNVD
Cervical cancer	21063398	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Oral cancer	21386901	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	22065749	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Basal cell lymphoma	21115979	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Myelodysplastic syndrome	21251322	CNVD
Breast cancer	16608533	CNVD
Acute myeloid leukemia	20729466	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21785460	CNVD
Breast cancer	17133270	CNVD
Cancer	16751803	CNVD
abnormal development	18461090	CNVD
Autism	19653912	CNVD
small cell lung cancer	20016488	CNVD
Cancer	20164920	CNVD
Prostate cancer	18632612	CNVD
Cervical cancer	21062161	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Austim spectrum disorder	21302340	CNVD
Colorectal cancer	16272173	CNVD
Breast cancer	16397240	CNVD
Epilepsy	20736978	CNVD
Mental retardation	20736978	CNVD
speech impairment	20736978	CNVD
Intracranial aneurysm	16715129	CNVD
Esophageal squamous carcinoma	17470683	CNVD
Mental retardation	17124404	CNVD
Congenital anomalies of the kidney and urinary tract	20299530	CNVD
Developmental delay	21147756	CNVD
Breast cancer	21509527	CNVD
Cancer	21129771	CNVD
Myelofibrosis	22110671	CNVD
Neurodevelopmental disorder	16760732	CNVD
Schizophrenia	22118685	CNVD
Schizophrenia	22958593	CNVD
Schizophrenia	21285140	CNVD
Schizophrenia	20970697	CNVD
Mental retardation	19951919	CNVD
Autism	20970697	CNVD
Developmental delay	18471269	CNVD
Intellectual disability	22045946	CNVD
Breast cancer	21045282	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Ovarian cancer	20844748	CNVD
Adenocarcinoma	19607727	CNVD
Squamous cell cancer	19607727	CNVD
Uveal melanoma	20484589	CNVD
3q29 microdeletion syndrome	20500065	CNVD
Biliary cancer	20453639	CNVD
3q29 microdeletion syndrome	22283845	CNVD
3q29 microdeletion syndrome	21626679	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Ovarian cancer	21720365	CNVD
Breast cancer	21364760	CNVD
Urothelial carcinoma	21177765	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:1243 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:195919400-195929400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr3:195920000-195929400	Weak transcription	HUES6 Cell Line	embryonic stem cell
3	chr3:195920200-195930400	Weak transcription	Esophagus	oesophagus
4	chr3:195920200-195930600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
5	chr3:195921000-195928800	Weak transcription	Stomach Smooth Muscle	stomach
6	chr3:195921200-195929400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
7	chr3:195921400-195929000	Weak transcription	Primary B cells from cord blood	blood
8	chr3:195921400-195929600	Weak transcription	Brain Anterior Caudate	brain
9	chr3:195921600-195929200	Weak transcription	Fetal Muscle Leg	muscle
10	chr3:195921600-195934000	Weak transcription	Right Atrium	heart
11	chr3:195921800-195929400	Weak transcription	Rectal Mucosa Donor 29	rectum
12	chr3:195922000-195934200	Weak transcription	Right Ventricle	heart
13	chr3:195923600-195928800	Weak transcription	Monocytes-CD14+_RO01746	blood
14	chr3:195923600-195929000	Weak transcription	Primary monocytes fromperipheralblood	blood
15	chr3:195923600-195929000	Weak transcription	K562	blood
16	chr3:195923600-195929400	Weak transcription	Cortex derived primary cultured neurospheres	brain
17	chr3:195923600-195929600	Weak transcription	Rectal Mucosa Donor 31	rectum
18	chr3:195923600-195930200	Weak transcription	Duodenum Mucosa	Duodenum
19	chr3:195923800-195930200	Weak transcription	Spleen	Spleen
20	chr3:195923800-195934200	Weak transcription	Thymus	Thymus
21	chr3:195924000-195929200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
22	chr3:195924200-195927000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
23	chr3:195924200-195929000	Weak transcription	Primary B cells from peripheral blood	blood
24	chr3:195924400-195926400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
25	chr3:195924400-195929000	Weak transcription	Placenta	Placenta
26	chr3:195924600-195929400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
27	chr3:195925600-195926400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
28	chr3:195925600-195926400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
29	chr3:195925600-195926400	Enhancers	Ovary	ovary
30	chr3:195925800-195926600	Bivalent Enhancer	HepG2	liver
31	chr3:195925800-195928800	Weak transcription	Primary neutrophils fromperipheralblood	blood
32	chr3:195926200-195929000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
33	chr3:195926200-195929200	Weak transcription	Adipose Nuclei	Adipose
34	chr3:195926400-195929400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
35	chr3:195926400-195929400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
36	chr3:195926400-195929400	Weak transcription	Ovary	ovary
37	chr3:195927000-195929200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
38	chr3:195928600-195928800	Enhancers	Duodenum Smooth Muscle	Duodenum
39	chr3:195928800-195929200	Enhancers	Primary neutrophils fromperipheralblood	blood
40	chr3:195928800-195929200	Enhancers	Stomach Smooth Muscle	stomach
41	chr3:195928800-195929200	Enhancers	Monocytes-CD14+_RO01746	blood
42	chr3:195928800-195929600	Weak transcription	Colonic Mucosa	Colon
43	chr3:195929000-195929200	Enhancers	HepG2	liver
44	chr3:195929000-195929800	Enhancers	K562	blood
45	chr3:195929000-195930400	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
46	chr3:195929000-195930800	Enhancers	Placenta	Placenta
47	chr3:195929000-195931600	Enhancers	Primary B cells from cord blood	blood
48	chr3:195929000-195931600	Enhancers	Primary B cells from peripheral blood	blood
49	chr3:195929000-195932000	Enhancers	Primary monocytes fromperipheralblood	blood
50	chr3:195929200-195929400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived

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