Variant report

Variant	nsv933192
Chromosome Location	chr3:121544496-121575871
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:822)
CpG islands
(count:977)
Chromatin interactive
region (count:37)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:822 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr3:121553892-121554340	HepG2	liver:	n/a	n/a
2	ARID3A	chr3:121553786-121554196	K562	blood:	n/a	n/a
3	ARID3A	chr3:121555327-121555897	K562	blood:	n/a	n/a
4	ATF2	chr3:121553346-121554690	GM12878	blood:	n/a	n/a
5	ATF2	chr3:121553559-121554147	GM12878	blood:	n/a	n/a
6	BACH1	chr3:121553761-121554262	H1-hESC	embryonic stem cell:	n/a	n/a
7	BACH1	chr3:121554053-121554074	K562	blood:	n/a	n/a
8	BATF	chr3:121553976-121554220	GM12878	blood:	n/a	n/a
9	BATF	chr3:121553884-121554288	GM12878	blood:	n/a	n/a
10	BCLAF1	chr3:121553367-121554432	GM12878	blood:	n/a	chr3:121553872-121553885 chr3:121553949-121553958
11	BCLAF1	chr3:121553167-121554413	GM12878	blood:	n/a	chr3:121553872-121553885 chr3:121553949-121553958
12	BHLHE40	chr3:121553728-121554278	GM12878	blood:	n/a	n/a
13	BHLHE40	chr3:121553722-121554638	K562	blood:	n/a	n/a
14	BRCA1	chr3:121554068-121554078	H1-hESC	embryonic stem cell:	n/a	n/a
15	BRCA1	chr3:121553701-121553956	HepG2	liver:	n/a	n/a
16	BRCA1	chr3:121553955-121554379	GM12878	blood:	n/a	n/a
17	BRCA1	chr3:121553336-121554583	Hela-S3	cervix:	n/a	n/a
18	CBX3	chr3:121553593-121554309	K562	blood:	n/a	n/a
19	CCNT2	chr3:121554572-121554734	K562	blood:	n/a	n/a
20	CCNT2	chr3:121553632-121554314	K562	blood:	n/a	n/a
21	CEBPB	chr3:121552894-121553455	HepG2	liver:	n/a	chr3:121553081-121553092
22	CEBPB	chr3:121553773-121554239	H1-hESC	embryonic stem cell:	n/a	chr3:121553973-121553981
23	CEBPB	chr3:121575385-121575502	K562	blood:	n/a	n/a
24	CEBPB	chr3:121552889-121553289	HepG2	liver:	n/a	chr3:121553081-121553092
25	CEBPB	chr3:121552665-121553617	MCF-7	breast:	n/a	chr3:121553081-121553092
26	CEBPB	chr3:121552888-121554080	IMR90	lung:	n/a	chr3:121553973-121553981 chr3:121553081-121553092
27	CEBPB	chr3:121565391-121565426	H1-hESC	embryonic stem cell:	n/a	n/a
28	CEBPB	chr3:121552599-121554117	Hela-S3	cervix:	n/a	chr3:121553973-121553981 chr3:121553081-121553092
29	CEBPB	chr3:121552769-121553424	ECC-1	luminal epithelium:	n/a	chr3:121553081-121553092
30	CEBPB	chr3:121552725-121553541	HCT-116	colon:	n/a	chr3:121553081-121553092
31	CEBPB	chr3:121553617-121553886	HepG2	liver:	n/a	n/a
32	CEBPB	chr3:121552777-121553554	A549	lung:	n/a	chr3:121553081-121553092
33	CEBPB	chr3:121552818-121553328	H1-hESC	embryonic stem cell:	n/a	chr3:121553081-121553092
34	CEBPB	chr3:121552902-121553198	K562	blood:	n/a	chr3:121553081-121553092
35	CEBPB	chr3:121552820-121553281	HepG2	liver:	n/a	chr3:121553081-121553092
36	CEBPB	chr3:121552753-121553459	MCF-7	breast:	n/a	chr3:121553081-121553092
37	CEBPB	chr3:121552776-121553319	A549	lung:	n/a	chr3:121553081-121553092
38	CEBPB	chr3:121552889-121553361	A549	lung:	n/a	chr3:121553081-121553092
39	CEBPB	chr3:121552803-121553404	HCT-116	colon:	n/a	chr3:121553081-121553092
40	CEBPB	chr3:121552942-121553212	HepG2	liver:	n/a	chr3:121553081-121553092
41	CEBPB	chr3:121552749-121553502	ECC-1	luminal epithelium:	n/a	chr3:121553081-121553092
42	CEBPB	chr3:121553669-121553934	K562	blood:	n/a	n/a
43	CEBPB	chr3:121552693-121553904	K562	blood:	n/a	chr3:121553081-121553092
44	CEBPB	chr3:121552806-121553326	K562	blood:	n/a	chr3:121553081-121553092
45	CEBPB	chr3:121556651-121556878	HepG2	liver:	n/a	chr3:121556793-121556804
46	CEBPB	chr3:121553565-121554796	GM12878	blood:	n/a	chr3:121553973-121553981
47	CEBPB	chr3:121556656-121556974	K562	blood:	n/a	chr3:121556793-121556804
48	CEBPD	chr3:121553592-121554212	HepG2	liver:	n/a	n/a
49	CEBPD	chr3:121552953-121553194	HepG2	liver:	n/a	chr3:121553082-121553093
50	CHD1	chr3:121553655-121555123	GM12878	blood:	n/a	chr3:121554351-121554361

(count:977 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:121553721-121553771	HepG2	liver:	n/a
2	chr3:121553721-121553771	HepG2	liver:	n/a
3	chr3:121554459-121554509	BJ	skin:	n/a
4	chr3:121553940-121553990	HUVEC	blood vessel:	n/a
5	chr3:121556543-121556593	GM12892	blood:	n/a
6	chr3:121555186-121555236	K562	blood:	n/a
7	chr3:121553361-121553411	GM12891	blood:	n/a
8	chr3:121554094-121554144	HIPEpiC	eye:	n/a
9	chr3:121553821-121553871	HRCEpiC	kidney:	n/a
10	chr3:121554169-121554219	HCM	heart:	n/a
11	chr3:121554094-121554144	IMR90	lung:	fetal
12	chr3:121554094-121554144	GM19239	blood:	n/a
13	chr3:121554169-121554219	AG09309	skin:	n/a
14	chr3:121553821-121553871	HIPEpiC	eye:	n/a
15	chr3:121553992-121554042	GM06990	blood:	n/a
16	chr3:121556543-121556593	HRPEpiC	eye:	n/a
17	chr3:121553940-121553990	A549	lung:	n/a
18	chr3:121553721-121553771	HRCEpiC	kidney:	n/a
19	chr3:121553821-121553871	H1-hESC	embryonic stem cell:	embryo
20	chr3:121554012-121554062	MCF-7	breast:	n/a
21	chr3:121555186-121555236	Caco-2	colon:	n/a
22	chr3:121553821-121553871	PrEC	prostate:	n/a
23	chr3:121554015-121554065	HCPEpiC	choroid plexus:	n/a
24	chr3:121554459-121554509	AG10803	skin:	n/a
25	chr3:121556543-121556593	HCT-116	colon:	n/a
26	chr3:121554166-121554216	HCM	heart:	n/a
27	chr3:121553721-121553771	NT2-D1	testis:	n/a
28	chr3:121553821-121553871	HRE	kidney:	n/a
29	chr3:121553940-121553990	HEK293	kidney:	embryo
30	chr3:121554012-121554062	HCM	heart:	n/a
31	chr3:121553985-121554035	AG04449	skin:	fetal
32	chr3:121554459-121554509	AG09309	skin:	n/a
33	chr3:121553586-121553636	RPTEC	kidney:	n/a
34	chr3:121553821-121553871	AoSMC	blood vessel:	n/a
35	chr3:121554019-121554069	BE2_C	brain:	n/a
36	chr3:121554015-121554065	HepG2	liver:	n/a
37	chr3:121555186-121555236	HEEpiC	esophagus:	n/a
38	chr3:121554015-121554065	HCF	heart:	n/a
39	chr3:121554012-121554062	HUVEC	blood vessel:	n/a
40	chr3:121553940-121553990	MCF-7	breast:	n/a
41	chr3:121553940-121553990	ovcar-3	ovarian:	n/a
42	chr3:121554094-121554144	HPAEpiC	pulmonary alveolar:	n/a
43	chr3:121554019-121554069	Jurkat	blood:	n/a
44	chr3:121553721-121553771	LNCaP	prostate:	n/a
45	chr3:121554019-121554069	HPAEpiC	pulmonary alveolar:	n/a
46	chr3:121553985-121554035	T-47D	breast:	n/a
47	chr3:121554012-121554062	SK-N-SH_RA	brain:	n/a
48	chr3:121556543-121556593	HepG2	liver:	n/a
49	chr3:121553586-121553636	SK-N-SH	brain:	n/a
50	chr3:121553821-121553871	GM12891	blood:	n/a

(count:37 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr3:121552701..121555986-chr3:121566308..121570556,4	MCF-7	breast:
2	chr3:121574320..121575023-chr3:121811100..121811983,4	MCF-7	breast:
3	chr3:121559897..121561834-chr3:121567497..121569683,2	MCF-7	breast:
4	chr3:121540007..121542032-chr3:121549979..121552263,2	K562	blood:
5	chr3:121553730..121556319-chr3:121561378..121563069,2	MCF-7	breast:
6	chr3:121574042..121575089-chr3:121714066..121715464,7	MCF-7	breast:
7	chr3:121557805..121560130-chr3:121563669..121566331,2	MCF-7	breast:
8	chr3:121377179..121379153-chr3:121573085..121574882,2	MCF-7	breast:
9	chr3:121566038..121567568-chr3:121569275..121571033,2	K562	blood:
10	chr3:121552093..121553677-chr3:122102440..122104911,2	K562	blood:
11	chr3:121553807..121555677-chr3:121556073..121558919,2	K562	blood:
12	chr3:121541912..121545321-chr3:121545405..121548683,3	MCF-7	breast:
13	chr19:58897685..58898333-chr3:121553940..121554762,2	NB4	blood:
14	chr3:121552695..121555483-chr3:122101751..122103619,2	MCF-7	breast:
15	chr3:121547606..121551491-chr3:121552024..121556641,8	K562	blood:
16	chr3:121571415..121571970-chr3:121831459..121832214,2	MCF-7	breast:
17	chr3:121573144..121575640-chr3:121713880..121715602,2	MCF-7	breast:
18	chr3:121574242..121575122-chr3:121708627..121709453,3	MCF-7	breast:
19	chr3:121574545..121575050-chr3:121977317..121977833,2	MCF-7	breast:
20	chr3:121554035..121556344-chr3:121572170..121574848,2	MCF-7	breast:
21	chr3:121541912..121545321-chr3:121545405..121548683,3	MCF-7	breast:
22	chr3:121544640..121546526-chr3:121557877..121559785,2	MCF-7	breast:
23	chr3:121544640..121546526-chr3:121557877..121559785,2	MCF-7	breast:
24	chr3:121559897..121561834-chr3:121567497..121569683,2	MCF-7	breast:
25	chr3:121537691..121539463-chr3:121547054..121549794,2	K562	blood:
26	chr3:121547116..121548952-chr3:121552697..121555325,4	MCF-7	breast:
27	chr3:121465799..121468529-chr3:121552939..121555166,2	MCF-7	breast:
28	chr3:121552749..121555082-chr3:121555544..121558140,3	MCF-7	breast:
29	chr3:121552259..121553812-chr3:121688554..121691121,2	MCF-7	breast:
30	chr3:121535928..121538474-chr3:121548099..121550812,2	K562	blood:
31	chr3:121466624..121468797-chr3:121553319..121555550,2	MCF-7	breast:
32	chr3:121557805..121560130-chr3:121563669..121566331,2	MCF-7	breast:
33	chr3:121542094..121547034-chr3:121547487..121555799,13	K562	blood:
34	chr3:121566038..121567568-chr3:121569275..121571033,2	K562	blood:
35	chr3:121574539..121575065-chr3:121708863..121709385,3	MCF-7	breast:
36	chr3:121552768..121555553-chr3:121556073..121559770,4	K562	blood:
37	chr3:121523456..121525541-chr3:121550635..121553696,3	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GOLGB1-3	chr3:121553813-121553839	NONHSAT091482
2	lnc-GOLGB1-3	chr3:121552783-121553326	NONHSAT091482

No data

Variant related genes	Relation type
IQCB1	TF binding region
EAF2	TF binding region
IQCB1	CpG island
EAF2	CpG island
ENSG00000173226	chromatin interactions
ENSG00000083845	chromatin interactions
ENSG00000145088	chromatin interactions
ENSG00000173230	chromatin interactions
ENSG00000114023	chromatin interactions
ENSG00000266640	chromatin interactions
ENSG00000160124	chromatin interactions

Extended variants
information (count: 1059 )
Associated
traits (count: 57 )

Variant overlapped rSNPs/rCNVs (count:1059 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs116922465	chr3:121544504-121544505	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs540039233	chr3:121544511-121544512	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs187937387	chr3:121544532-121544533	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs34142001	chr3:121544610-121544611	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs114162900	chr3:121544623-121544624	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs368018257	chr3:121544632-121544633	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs9857271	chr3:121544688-121544689	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs146228286	chr3:121544765-121544766	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs546830888	chr3:121544767-121544768	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs548274268	chr3:121544792-121544793	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs568172136	chr3:121544797-121544798	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs527842453	chr3:121544846-121544847	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs534325743	chr3:121544847-121544848	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs369407077	chr3:121544883-121544884	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs139299149	chr3:121544943-121544944	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs369191532	chr3:121544964-121544965	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs146580215	chr3:121544969-121544970	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs376703708	chr3:121545003-121545004	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs370233738	chr3:121545019-121545020	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs199800276	chr3:121545037-121545038	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs376353341	chr3:121545039-121545040	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs569996040	chr3:121545044-121545045	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs115133919	chr3:121545048-121545049	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs371889279	chr3:121545070-121545071	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs555393018	chr3:121545104-121545105	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs192049433	chr3:121545144-121545145	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs144117502	chr3:121545160-121545161	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs553969510	chr3:121545161-121545162	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs371857548	chr3:121545205-121545206	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs78742442	chr3:121545235-121545236	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs546053137	chr3:121545260-121545261	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs562656405	chr3:121545301-121545302	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs75133035	chr3:121545367-121545368	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs375099509	chr3:121545445-121545446	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs184369561	chr3:121545530-121545531	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs547575259	chr3:121545551-121545552	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs189665380	chr3:121545552-121545553	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs4505751	chr3:121545661-121545662	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
39	rs192744120	chr3:121545674-121545675	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs567741267	chr3:121545675-121545676	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs115142078	chr3:121545686-121545687	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs533374121	chr3:121545696-121545697	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs373524402	chr3:121545732-121545733	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs184297707	chr3:121545738-121545739	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs370958643	chr3:121545845-121545846	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs146512331	chr3:121545861-121545862	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs555384715	chr3:121545878-121545879	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs556848007	chr3:121545928-121545929	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs148697740	chr3:121545954-121545955	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs534821862	chr3:121545976-121545977	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:57)

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
Cancer	21183584	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Bipolar disorder	20877625	CNVD
Bipolar disorder	21956041	CNVD
Bipolar disorder	22241247	CNVD
Biliary cancer	18923514	CNVD
Prostate cancer	21965145	CNVD
Cancer	21129771	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Cervical cancer	21062161	CNVD
Squamous cell cancer	20885788	CNVD
Melanoma	18172304	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Bipolar disorder	18458673	CNVD
Breast cancer	22032731	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Breast cancer	16461572	CNVD
Neuroblastoma	17533364	CNVD
microdeletion syndrome	22180640	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
Breast cancer	16608533	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Developmental delay	22180640	CNVD
Multiple myeloma	17550852	CNVD
Basal cell lymphoma	21115979	CNVD
Ovarian cancer	22174824	CNVD
lymphocytic leukemia	21291569	CNVD
small cell lung cancer	20016488	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Autism	22241247	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:955 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:121491600-121552600	Weak transcription	NHLF	lung
2	chr3:121507000-121545400	Weak transcription	Fetal Heart	heart
3	chr3:121528000-121553000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
4	chr3:121530800-121552200	Weak transcription	Small Intestine	intestine
5	chr3:121530800-121552400	Weak transcription	Brain Cingulate Gyrus	brain
6	chr3:121530800-121552800	Weak transcription	HSMMtube	muscle
7	chr3:121530800-121553000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr3:121530800-121553200	Weak transcription	Esophagus	oesophagus
9	chr3:121531000-121552800	Weak transcription	Fetal Stomach	stomach
10	chr3:121531000-121552800	Weak transcription	Pancreas	Pancrea
11	chr3:121531000-121552800	Weak transcription	Right Ventricle	heart
12	chr3:121531000-121552800	Weak transcription	Spleen	Spleen
13	chr3:121531200-121549600	Weak transcription	Brain Angular Gyrus	brain
14	chr3:121534200-121544600	Weak transcription	Brain Substantia Nigra	brain
15	chr3:121535400-121551200	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
16	chr3:121535600-121545200	ZNF genes & repeats	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
17	chr3:121536000-121551600	Strong transcription	Fetal Thymus	thymus
18	chr3:121536200-121552800	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
19	chr3:121536400-121548000	Strong transcription	Rectal Mucosa Donor 29	rectum
20	chr3:121537200-121552600	Weak transcription	Rectal Smooth Muscle	rectum
21	chr3:121537400-121552800	Weak transcription	H9 Cell Line	embryonic stem cell
22	chr3:121538400-121552000	Weak transcription	Gastric	stomach
23	chr3:121539200-121547000	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
24	chr3:121539600-121548200	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
25	chr3:121539800-121547400	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
26	chr3:121539800-121548200	Strong transcription	Liver	Liver
27	chr3:121539800-121552600	Strong transcription	HUES48 Cell Line	embryonic stem cell
28	chr3:121539800-121552600	Strong transcription	HSMM	muscle
29	chr3:121540000-121547200	ZNF genes & repeats	GM12878-XiMat	blood
30	chr3:121540000-121547400	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
31	chr3:121540000-121547400	Strong transcription	Rectal Mucosa Donor 31	rectum
32	chr3:121540000-121547400	Strong transcription	Hela-S3	cervix
33	chr3:121540000-121548200	Strong transcription	Primary monocytes fromperipheralblood	blood
34	chr3:121540000-121552000	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
35	chr3:121540200-121544800	Strong transcription	Primary T helper naive cells from peripheral blood	blood
36	chr3:121540200-121547400	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--
37	chr3:121540200-121549000	Strong transcription	Placenta	Placenta
38	chr3:121541000-121548200	Strong transcription	Skeletal Muscle Female	skeletal muscle
39	chr3:121541200-121547400	Strong transcription	Primary T killer naive cells fromperipheralblood	blood
40	chr3:121541200-121553000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
41	chr3:121541400-121546400	Strong transcription	Primary T killer memory cells from peripheral blood	blood
42	chr3:121541400-121548400	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
43	chr3:121541400-121552800	Weak transcription	Aorta	Aorta
44	chr3:121541600-121546400	Strong transcription	Osteobl	bone
45	chr3:121541600-121550000	Weak transcription	Psoas Muscle	Psoas
46	chr3:121541600-121552800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
47	chr3:121541800-121545200	Strong transcription	NHEK	skin
48	chr3:121542200-121552800	Weak transcription	Left Ventricle	heart
49	chr3:121542400-121544600	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
50	chr3:121542400-121546600	Strong transcription	Primary T helper memory cells from peripheral blood 1	blood

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