Variant report

Variant	nsv471425
Chromosome Location	chr3:49721381-49726196
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:339)
CpG islands
(count:366)
Chromatin interactive
region (count:21)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:339 , 50 per page) page: 1 2 3 4 5 6 7

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BCL11A	chr3:49722968-49723129	GM12878	blood:	n/a	n/a
2	BRCA1	chr3:49726122-49726173	HepG2	liver:	n/a	n/a
3	CBX3	chr3:49725844-49727257	K562	blood:	n/a	n/a
4	CBX3	chr3:49723474-49724174	K562	blood:	n/a	n/a
5	CEBPB	chr3:49725999-49726205	K562	blood:	n/a	chr3:49726131-49726142
6	CEBPB	chr3:49725976-49726336	HepG2	liver:	n/a	chr3:49726131-49726142
7	CEBPB	chr3:49725976-49726402	HepG2	liver:	n/a	chr3:49726131-49726142
8	CEBPB	chr3:49725936-49727036	K562	blood:	n/a	chr3:49726131-49726142
9	CEBPB	chr3:49726094-49726245	HepG2	liver:	n/a	chr3:49726131-49726142
10	CEBPB	chr3:49726073-49726639	K562	blood:	n/a	chr3:49726131-49726142
11	CEBPD	chr3:49726024-49726402	HepG2	liver:	n/a	chr3:49726130-49726141
12	CEBPD	chr3:49726053-49727801	K562	blood:	n/a	chr3:49726130-49726141
13	CEBPD	chr3:49726080-49726365	HepG2	liver:	n/a	chr3:49726130-49726141
14	CHD2	chr3:49726138-49726277	HepG2	liver:	n/a	n/a
15	CTCF	chr3:49721937-49722113	MCF-7	breast:	n/a	n/a
16	CTCF	chr3:49721979-49722107	MCF-7	breast:	n/a	n/a
17	CTCF	chr3:49721940-49722090	GM12867	blood:	n/a	n/a
18	CTCF	chr3:49721980-49722130	HBMEC	blood vessel:	n/a	n/a
19	CTCF	chr3:49721985-49722053	Hela-S3	cervix:	n/a	n/a
20	CTCF	chr3:49721980-49722091	MCF-7	breast:	n/a	n/a
21	CTCF	chr3:49721900-49722050	GM12875	blood:	n/a	n/a
22	CTCF	chr3:49723880-49724030	HRE	kidney:	n/a	n/a
23	CTCF	chr3:49721880-49722030	RPTEC	kidney:	n/a	n/a
24	CTCF	chr3:49721980-49722130	GM12864	blood:	n/a	n/a
25	CTCF	chr3:49721974-49722093	MCF-7	breast:	n/a	n/a
26	CTCF	chr3:49722018-49722021	K562	blood:	n/a	n/a
27	CTCF	chr3:49722060-49722210	GM06990	blood:	n/a	n/a
28	CTCF	chr3:49722040-49722190	HMEC	breast:	n/a	n/a
29	CTCF	chr3:49723989-49724021	LNCaP	prostate:	n/a	n/a
30	CTCF	chr3:49721900-49722050	GM12864	blood:	n/a	n/a
31	CTCF	chr3:49724131-49724133	Pancreas_OC	pancreas:	n/a	n/a
32	CTCF	chr3:49722016-49722026	Kidney_OC	kidney:	n/a	n/a
33	CTCF	chr3:49723875-49723931	H1-hESC	embryonic stem cell:	n/a	n/a
34	CTCF	chr3:49722024-49722044	K562	blood:	n/a	n/a
35	CTCF	chr3:49724134-49724172	Pancreas_OC	pancreas:	n/a	n/a
36	CTCF	chr3:49721918-49722121	H1-hESC	embryonic stem cell:	n/a	n/a
37	CTCF	chr3:49721872-49722139	K562	blood:	n/a	n/a
38	CTCF	chr3:49723860-49724010	SK-N-SH_RA	brain:	n/a	n/a
39	CTCF	chr3:49722770-49722862	GM10266	blood:	n/a	n/a
40	CTCF	chr3:49721997-49722088	GM12891	blood:	n/a	n/a
41	CTCF	chr3:49721821-49722162	K562	blood:	n/a	n/a
42	CTCF	chr3:49721988-49722077	MCF-7	breast:	n/a	n/a
43	CTCF	chr3:49721966-49722092	HepG2	liver:	n/a	n/a
44	CTCF	chr3:49722011-49722064	GM10248	blood:	n/a	n/a
45	CTCF	chr3:49721857-49722316	K562	blood:	n/a	n/a
46	CTCF	chr3:49722508-49722574	GM13976	blood:	n/a	n/a
47	CTCF	chr3:49721900-49722050	HepG2	liver:	n/a	n/a
48	CTCF	chr3:49721900-49722050	HEK293	kidney:	n/a	n/a
49	CTCF	chr3:49722008-49722053	A549	lung:	n/a	n/a
50	CTCF	chr3:49724147-49724168	H1-hESC	embryonic stem cell:	n/a	n/a

(count:366 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:49722237-49722287	MCF10A-Er-Src	breast:	n/a
2	chr3:49722237-49722287	CMK	blood:	n/a
3	chr3:49722237-49722287	AG04450	lung:	fetal
4	chr3:49724291-49724341	MCF-7	breast:	n/a
5	chr3:49724291-49724341	HepG2	liver:	n/a
6	chr3:49726151-49726201	GM06990	blood:	n/a
7	chr3:49723245-49723295	HNPCEpiC	eye:	n/a
8	chr3:49724254-49724304	MCF-7	breast:	n/a
9	chr3:49724291-49724341	K562	blood:	n/a
10	chr3:49723245-49723295	AG09319	gingival:	n/a
11	chr3:49724291-49724341	NT2-D1	testis:	n/a
12	chr3:49722237-49722287	HAEpiC	amniotic membrane:	n/a
13	chr3:49723245-49723295	Hepatocyte	liver:	n/a
14	chr3:49723245-49723295	NH-A	brain:	n/a
15	chr3:49722237-49722287	HCM	heart:	n/a
16	chr3:49724291-49724341	GM12878	blood:	n/a
17	chr3:49724291-49724341	BE2_C	brain:	n/a
18	chr3:49726151-49726201	HepG2	liver:	n/a
19	chr3:49726151-49726201	Hela-S3	cervix:	n/a
20	chr3:49723245-49723295	SK-N-SH	brain:	n/a
21	chr3:49724254-49724304	T-47D	breast:	n/a
22	chr3:49723947-49723997	SK-N-SH	brain:	n/a
23	chr3:49723245-49723295	HRPEpiC	eye:	n/a
24	chr3:49724291-49724341	SK-N-SH_RA	brain:	n/a
25	chr3:49724254-49724304	HEEpiC	esophagus:	n/a
26	chr3:49726151-49726201	NH-A	brain:	n/a
27	chr3:49723245-49723295	SKMC	muscle:	n/a
28	chr3:49723245-49723295	HepG2	liver:	n/a
29	chr3:49724254-49724304	HL-60	blood:	n/a
30	chr3:49726151-49726201	AG04450	lung:	fetal
31	chr3:49724254-49724304	MCF10A-Er-Src	breast:	n/a
32	chr3:49722237-49722287	LNCaP	prostate:	n/a
33	chr3:49723947-49723997	HRPEpiC	eye:	n/a
34	chr3:49724291-49724341	HL-60	blood:	n/a
35	chr3:49723947-49723997	Jurkat	blood:	n/a
36	chr3:49723947-49723997	LNCaP	prostate:	n/a
37	chr3:49726151-49726201	ECC-1	luminal epithelium:	n/a
38	chr3:49726151-49726201	LNCaP	prostate:	n/a
39	chr3:49726151-49726201	HCT-116	colon:	n/a
40	chr3:49726151-49726201	HL-60	blood:	n/a
41	chr3:49723947-49723997	Hela-S3	cervix:	n/a
42	chr3:49723947-49723997	GM06990	blood:	n/a
43	chr3:49722237-49722287	MCF-7	breast:	n/a
44	chr3:49724254-49724304	NH-A	brain:	n/a
45	chr3:49724291-49724341	NH-A	brain:	n/a
46	chr3:49724254-49724304	ECC-1	luminal epithelium:	n/a
47	chr3:49724254-49724304	BE2_C	brain:	n/a
48	chr3:49726151-49726201	GM12878	blood:	n/a
49	chr3:49723947-49723997	AG04449	skin:	fetal
50	chr3:49723947-49723997	HNPCEpiC	eye:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr1:16969549..16972758-chr3:49725610..49728945,8	K562	blood:
2	chr3:49448668..49451033-chr3:49723995..49726731,2	MCF-7	breast:
3	chr3:49722536..49724153-chr3:49724898..49727146,2	MCF-7	breast:
4	chr1:17086818..17089262-chr3:49723617..49726310,2	MCF-7	breast:
5	chr3:49724739..49727802-chr3:49735823..49739048,3	MCF-7	breast:
6	chr3:49719726..49722448-chr3:49723596..49725872,2	K562	blood:
7	chr1:16964923..16974624-chr3:49722461..49732046,16	K562	blood:
8	chr3:49724349..49727675-chr3:49755739..49757510,3	MCF-7	breast:
9	chr3:49709764..49714141-chr3:49724462..49728582,8	MCF-7	breast:
10	chr3:49708866..49715375-chr3:49724746..49730407,6	K562	blood:
11	chr3:49719547..49721441-chr3:49726309..49728909,2	K562	blood:
12	chr1:16969769..16972744-chr3:49724987..49728952,10	MCF-7	breast:
13	chr3:49719726..49722448-chr3:49723596..49725872,2	K562	blood:
14	chr3:49720877..49722933-chr3:49723247..49725096,3	K562	blood:
15	chr3:49715211..49719699-chr3:49722366..49724649,4	K562	blood:
16	chr3:49724901..49726999-chr3:49761086..49763587,3	MCF-7	breast:
17	chr3:49711727..49717769-chr3:49722772..49726950,7	K562	blood:
18	chr3:49722536..49724153-chr3:49724898..49727146,2	MCF-7	breast:
19	chr3:49720877..49722933-chr3:49723247..49725096,3	K562	blood:
20	chr1:16968825..16972400-chr3:49724902..49730445,9	MCF-7	breast:
21	chr3:49710552..49715225-chr3:49718907..49727364,14	MCF-7	breast:

No data

Variant related genes	Relation type
RNF123	TF binding region
ENSG00000259970	TF binding region
MST1	TF binding region
RNF123	CpG island
ENSG00000259970	CpG island
MST1	CpG island
ENSG00000173531	chromatin interactions
ENSG00000176020	chromatin interactions
ENSG00000067560	chromatin interactions
ENSG00000215908	chromatin interactions
ENSG00000186715	chromatin interactions
ENSG00000164062	chromatin interactions
ENSG00000145022	chromatin interactions
ENSG00000173540	chromatin interactions
ENSG00000259970	chromatin interactions
ENSG00000186301	chromatin interactions
ENSG00000164068	chromatin interactions

Extended variants
information (count: 344 )
Associated
traits (count: 99 )

Variant overlapped rSNPs/rCNVs (count:344 , 50 per page) page: 1 2 3 4 5 6 7

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs145946970	chr3:49721432-49721433	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
2	rs1057363	chr3:49721448-49721449	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs368191700	chr3:49721510-49721511	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs369736713	chr3:49721512-49721513	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs3197999	chr3:49721532-49721533	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance disease
6	rs201332029	chr3:49721533-49721534	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs397713690	chr3:49721542-49721543	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs397839869	chr3:49721550-49721551	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs370472291	chr3:49721554-49721555	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs1057319	chr3:49721561-49721562	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs397831743	chr3:49721571-49721572	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs373984021	chr3:49721572-49721573	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs536973531	chr3:49721588-49721589	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs141594671	chr3:49721592-49721593	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs138238101	chr3:49721606-49721607	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs143118019	chr3:49721607-49721608	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs141810913	chr3:49721611-49721612	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs137880382	chr3:49721614-49721615	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs200268600	chr3:49721622-49721623	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs371334584	chr3:49721623-49721624	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs577003673	chr3:49721652-49721653	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs201428113	chr3:49721653-49721654	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs545095311	chr3:49721663-49721664	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs375990239	chr3:49721717-49721718	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs150531640	chr3:49721755-49721756	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs572214141	chr3:49721766-49721767	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs542575850	chr3:49721767-49721768	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs193164866	chr3:49721773-49721774	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs144922761	chr3:49721781-49721782	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs142824153	chr3:49721789-49721790	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs112084304	chr3:49721792-49721793	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs199810403	chr3:49721797-49721798	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs13085791	chr3:49721798-49721799	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
34	rs201444451	chr3:49721800-49721801	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs111260825	chr3:49721805-49721806	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs138629762	chr3:49721809-49721810	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs138155786	chr3:49721811-49721812	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs142690032	chr3:49721812-49721813	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs545657574	chr3:49721830-49721831	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs17854561	chr3:49721837-49721838	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs371353612	chr3:49721866-49721867	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs375757574	chr3:49721877-49721878	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs532706844	chr3:49721883-49721884	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs548020547	chr3:49721891-49721892	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs564275433	chr3:49721991-49721992	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs531549210	chr3:49721995-49721996	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs565746554	chr3:49721997-49721998	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs368735314	chr3:49722006-49722007	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs141182115	chr3:49722014-49722015	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs372578885	chr3:49722024-49722025	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:99)

Disease	PMID	Source
Lynch syndrome	18415027	CNVD
Renal cell carcinoma	18592004	CNVD
Acute myeloid leukemia	20729466	CNVD
Urothelial carcinoma	18382360	CNVD
Melanoma	18172304	CNVD
Cervical cancer	21062161	CNVD
Hirschsprung''s Disease	21712996	CNVD
Glioblastoma multiforme	21080181	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Insulin resistance	16721378	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	21484798	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Oral cancer	19627613	CNVD
Renal cell carcinoma	19461508	CNVD
Epithelial cancer	22065749	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Acute myeloid leukemia	16864856	CNVD
Liposarcoma	21253554	CNVD
Basal cell lymphoma	21115979	CNVD
Endometrial cancer	22040021	CNVD
Pancreatic endocrine tumor	20981439	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	17387387	CNVD
Oral cancer	21386901	CNVD
Cutaneous squamous cell carcinomas	19131950	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Retinoblastoma	21504564	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Renal cell carcinoma	21668985	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Thoracic aortic aneurysm	21092924	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	17603634	CNVD
Esophageal cancer	20955586	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Breast cancer	17133270	CNVD
Uveal melanoma	20484589	CNVD
Autism	22495311	CNVD
Melanoma	20688739	CNVD
Acute myeloid leukemia	21251322	CNVD
Hepatocellular carcinoma	16750200	CNVD
Cancer	21183584	CNVD
Kartagener syndrome	16639409	CNVD
Biliary cancer	19435499	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Bipolar disorder	20877625	CNVD
Bipolar disorder	21956041	CNVD
Bipolar disorder	22241247	CNVD
Biliary cancer	18923514	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	16397240	CNVD
Breast cancer	22032731	CNVD
Non-small cell lung cancer	20864512	CNVD
Colorectal cancer	16912164	CNVD
Non-small cell lung cancer	19010865	CNVD
Colorectal cancer	16272173	CNVD
Non-muscle invasive bladder neoplasm	19445696	CNVD
Acute myeloid leukemia	17268525	CNVD
Salivary gland tumor	18059337	CNVD
Gastric cancer	16891809	CNVD
Night blindness	17160897	CNVD
Cancer	17160897	CNVD
Breast cancer	20409316	CNVD
Lung cancer	17297452	CNVD
Multiple myeloma	16616336	CNVD
Effusion lymphoma	18079361	CNVD
Neuroblastoma	20406844	CNVD
Breast cancer	21785460	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	21045282	CNVD
Urothelial cell carcinoma	18451213	CNVD
Neuroblastoma	17327916	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Medullary thyroid carcinoma	18765511	CNVD
abnormal development	18461090	CNVD
Developmental delay	21147756	CNVD
Urothelial carcinoma	21177765	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Adrenocortical carcinoma	18281524	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:649 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:49712200-49723800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
2	chr3:49712800-49722200	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
3	chr3:49712800-49722200	Strong transcription	Fetal Stomach	stomach
4	chr3:49712800-49723600	Weak transcription	Right Atrium	heart
5	chr3:49712800-49726200	Weak transcription	Small Intestine	intestine
6	chr3:49713000-49721400	Strong transcription	NHEK	skin
7	chr3:49713000-49721600	Strong transcription	iPS-18 Cell Line	embryonic stem cell
8	chr3:49713000-49721600	Strong transcription	Brain Substantia Nigra	brain
9	chr3:49713000-49721600	Strong transcription	NHLF	lung
10	chr3:49713000-49722000	Strong transcription	HUES48 Cell Line	embryonic stem cell
11	chr3:49713000-49722000	Strong transcription	Stomach Smooth Muscle	stomach
12	chr3:49713000-49722200	Strong transcription	Duodenum Smooth Muscle	Duodenum
13	chr3:49713000-49722400	Strong transcription	H9 Cell Line	embryonic stem cell
14	chr3:49713000-49722400	Strong transcription	Cortex derived primary cultured neurospheres	brain
15	chr3:49713000-49722600	Strong transcription	HUES6 Cell Line	embryonic stem cell
16	chr3:49713000-49722800	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
17	chr3:49713000-49722800	Strong transcription	Thymus	Thymus
18	chr3:49713000-49723200	Weak transcription	Stomach Mucosa	stomach
19	chr3:49713000-49723400	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
20	chr3:49713000-49723800	Weak transcription	Fetal Heart	heart
21	chr3:49713200-49721400	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
22	chr3:49713200-49721400	Strong transcription	Colon Smooth Muscle	Colon
23	chr3:49713200-49721400	Strong transcription	Left Ventricle	heart
24	chr3:49713200-49721600	Strong transcription	Rectal Smooth Muscle	rectum
25	chr3:49713200-49721800	Strong transcription	H1 Cell Line	embryonic stem cell
26	chr3:49713200-49721800	Strong transcription	Primary monocytes fromperipheralblood	blood
27	chr3:49713200-49722000	Strong transcription	iPS DF 6.9 Cell Line	embryonic stem cell
28	chr3:49713200-49722000	Strong transcription	Brain Inferior Temporal Lobe	brain
29	chr3:49713200-49722000	Strong transcription	Rectal Mucosa Donor 29	rectum
30	chr3:49713200-49722200	Strong transcription	HUES64 Cell Line	embryonic stem cell
31	chr3:49713200-49722200	Strong transcription	iPS-15b Cell Line	embryonic stem cell
32	chr3:49713200-49722200	Strong transcription	Placenta	Placenta
33	chr3:49713200-49722400	Strong transcription	iPS-20b Cell Line	embryonic stem cell
34	chr3:49713200-49722400	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
35	chr3:49713200-49722400	Strong transcription	Primary hematopoietic stem cells short term culture	blood
36	chr3:49713200-49722400	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
37	chr3:49713200-49722400	Strong transcription	Monocytes-CD14+_RO01746	blood
38	chr3:49713200-49722600	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
39	chr3:49713200-49722600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
40	chr3:49713200-49722600	Strong transcription	Brain Germinal Matrix	brain
41	chr3:49713200-49722800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
42	chr3:49713200-49723000	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
43	chr3:49713200-49723000	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
44	chr3:49713400-49721400	Strong transcription	Aorta	Aorta
45	chr3:49713400-49721400	Strong transcription	Hela-S3	cervix
46	chr3:49713400-49721600	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
47	chr3:49713400-49721600	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--
48	chr3:49713400-49721600	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
49	chr3:49713400-49721600	Strong transcription	Fetal Lung	lung
50	chr3:49713400-49722000	Strong transcription	Brain Anterior Caudate	brain

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