Variant report

Variant	nsv1007373
Chromosome Location	chr3:23367952-23710331
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2297)
CpG islands
(count:1099)
Chromatin interactive
region (count:81)
LncRNA
region (count:7)
Mature miRNA
region (count: 0)
miRNA target
sites (count:1)

(count:2297 , 50 per page) page: 1 2 3 4 5 6 7 ... 46

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr3:23632245-23632882	GM12878	blood:	n/a	n/a
2	ATF2	chr3:23694976-23695742	GM12878	blood:	n/a	n/a
3	ATF2	chr3:23382835-23383365	GM12878	blood:	n/a	n/a
4	ATF2	chr3:23632265-23632852	GM12878	blood:	n/a	n/a
5	ATF2	chr3:23691709-23692219	GM12878	blood:	n/a	n/a
6	ATF2	chr3:23691746-23692150	GM12878	blood:	n/a	n/a
7	ATF2	chr3:23472393-23472877	GM12878	blood:	n/a	n/a
8	ATF2	chr3:23694962-23696476	GM12878	blood:	n/a	n/a
9	ATF3	chr3:23709678-23710369	A549	lung:	n/a	n/a
10	BACH1	chr3:23533686-23533737	H1-hESC	embryonic stem cell:	n/a	n/a
11	BACH1	chr3:23642660-23642857	H1-hESC	embryonic stem cell:	n/a	n/a
12	BACH1	chr3:23647847-23647871	H1-hESC	embryonic stem cell:	n/a	n/a
13	BACH1	chr3:23585155-23585177	K562	blood:	n/a	n/a
14	BACH1	chr3:23636852-23637069	K562	blood:	n/a	n/a
15	BATF	chr3:23696049-23696315	GM12878	blood:	n/a	n/a
16	BATF	chr3:23436607-23436931	GM12878	blood:	n/a	chr3:23436755-23436764
17	BATF	chr3:23695123-23695549	GM12878	blood:	n/a	n/a
18	BATF	chr3:23480171-23480448	GM12878	blood:	n/a	n/a
19	BATF	chr3:23480155-23480444	GM12878	blood:	n/a	n/a
20	BATF	chr3:23696063-23696336	GM12878	blood:	n/a	n/a
21	BATF	chr3:23591928-23592183	GM12878	blood:	n/a	n/a
22	BATF	chr3:23710024-23710375	GM12878	blood:	n/a	chr3:23710257-23710267
23	BATF	chr3:23691776-23692121	GM12878	blood:	n/a	n/a
24	BATF	chr3:23463964-23464237	GM12878	blood:	n/a	n/a
25	BATF	chr3:23632471-23632803	GM12878	blood:	n/a	n/a
26	BATF	chr3:23581038-23581276	GM12878	blood:	n/a	n/a
27	BCL11A	chr3:23632511-23632777	GM12878	blood:	n/a	n/a
28	BCL11A	chr3:23632390-23632814	GM12878	blood:	n/a	n/a
29	BCL3	chr3:23708870-23709470	A549	lung:	n/a	chr3:23709205-23709214
30	BCL3	chr3:23694963-23695574	GM12878	blood:	n/a	chr3:23695235-23695244
31	BCL3	chr3:23632491-23632796	GM12878	blood:	n/a	n/a
32	BCL3	chr3:23708903-23710567	A549	lung:	n/a	chr3:23710256-23710265 chr3:23709205-23709214
33	BCL3	chr3:23644357-23644673	GM12878	blood:	n/a	n/a
34	BCL3	chr3:23621629-23622436	A549	lung:	n/a	n/a
35	BCL3	chr3:23709641-23710500	A549	lung:	n/a	chr3:23710256-23710265
36	BCL3	chr3:23617886-23618518	A549	lung:	n/a	n/a
37	BCLAF1	chr3:23695097-23695692	GM12878	blood:	n/a	chr3:23695235-23695244
38	BCLAF1	chr3:23696030-23696510	GM12878	blood:	n/a	n/a
39	BCLAF1	chr3:23632368-23632849	GM12878	blood:	n/a	n/a
40	BCLAF1	chr3:23694930-23695751	GM12878	blood:	n/a	chr3:23695235-23695244
41	BCLAF1	chr3:23591798-23592336	GM12878	blood:	n/a	n/a
42	BCLAF1	chr3:23632313-23632878	GM12878	blood:	n/a	n/a
43	BCLAF1	chr3:23463910-23464435	GM12878	blood:	n/a	n/a
44	BHLHE40	chr3:23429181-23429214	GM12878	blood:	n/a	n/a
45	BHLHE40	chr3:23665952-23665953	GM12878	blood:	n/a	n/a
46	BHLHE40	chr3:23694959-23695865	GM12878	blood:	n/a	n/a
47	BHLHE40	chr3:23609332-23609762	GM12878	blood:	n/a	n/a
48	BHLHE40	chr3:23632261-23632824	GM12878	blood:	n/a	n/a
49	BHLHE40	chr3:23691985-23692248	GM12878	blood:	n/a	n/a
50	BHLHE40	chr3:23700911-23701108	GM12878	blood:	n/a	n/a

(count:1099 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:23653462-23653512	HRCEpiC	kidney:	n/a
2	chr3:23653462-23653512	HRCEpiC	kidney:	n/a
3	chr3:23448023-23448073	Hepatocyte	liver:	n/a
4	chr3:23478304-23478354	HCT-116	colon:	n/a
5	chr3:23522396-23522446	SAEC	small airway:	n/a
6	chr3:23504894-23504944	SK-N-SH	brain:	n/a
7	chr3:23478304-23478354	K562	blood:	n/a
8	chr3:23504894-23504944	NB4	blood:	n/a
9	chr3:23687466-23687516	HCF	heart:	n/a
10	chr3:23478304-23478354	SK-N-SH_RA	brain:	n/a
11	chr3:23578676-23578726	GM06990	blood:	n/a
12	chr3:23632110-23632160	ovcar-3	ovarian:	n/a
13	chr3:23504894-23504944	Hela-S3	cervix:	n/a
14	chr3:23448023-23448073	HUVEC	blood vessel:	n/a
15	chr3:23632110-23632160	HCPEpiC	choroid plexus:	n/a
16	chr3:23548050-23548100	CMK	blood:	n/a
17	chr3:23496403-23496453	NT2-D1	testis:	n/a
18	chr3:23415040-23415090	BJ	skin:	n/a
19	chr3:23522396-23522446	HRE	kidney:	n/a
20	chr3:23567565-23567615	ProgFib	skin:	n/a
21	chr3:23691152-23691202	BE2_C	brain:	n/a
22	chr3:23687466-23687516	HEEpiC	esophagus:	n/a
23	chr3:23632110-23632160	AoSMC	blood vessel:	n/a
24	chr3:23631338-23631388	HUVEC	blood vessel:	n/a
25	chr3:23653462-23653512	PFSK-1	brain:	n/a
26	chr3:23448023-23448073	NB4	blood:	n/a
27	chr3:23578676-23578726	GM12878	blood:	n/a
28	chr3:23478304-23478354	PrEC	prostate:	n/a
29	chr3:23448023-23448073	NH-A	brain:	n/a
30	chr3:23504894-23504944	GM19239	blood:	n/a
31	chr3:23641714-23641764	T-47D	breast:	n/a
32	chr3:23641714-23641764	SKMC	muscle:	n/a
33	chr3:23631338-23631388	SAEC	small airway:	n/a
34	chr3:23504894-23504944	HCPEpiC	choroid plexus:	n/a
35	chr3:23567565-23567615	AoSMC	blood vessel:	n/a
36	chr3:23522396-23522446	HUVEC	blood vessel:	n/a
37	chr3:23496403-23496453	K562	blood:	n/a
38	chr3:23632110-23632160	T-47D	breast:	n/a
39	chr3:23650443-23650493	LNCaP	prostate:	n/a
40	chr3:23548050-23548100	SK-N-MC	brain:	n/a
41	chr3:23653462-23653512	HNPCEpiC	eye:	n/a
42	chr3:23496403-23496453	PANC-1	pancreas:	n/a
43	chr3:23691152-23691202	NT2-D1	testis:	n/a
44	chr3:23567565-23567615	HUVEC	blood vessel:	n/a
45	chr3:23504894-23504944	AG04449	skin:	fetal
46	chr3:23631338-23631388	PFSK-1	brain:	n/a
47	chr3:23641714-23641764	RPTEC	kidney:	n/a
48	chr3:23478304-23478354	AG10803	skin:	n/a
49	chr3:23578676-23578726	RPTEC	kidney:	n/a
50	chr3:23653462-23653512	K562	blood:	n/a

(count:81 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr3:23482059..23483566-chr3:23484032..23486053,2	MCF-7	breast:
2	chr3:23489983..23492292-chr3:23500438..23503341,2	MCF-7	breast:
3	chr3:23436371..23438292-chr3:23438375..23440407,2	MCF-7	breast:
4	chr3:23594511..23597259-chr3:23606854..23610185,3	MCF-7	breast:
5	chr3:23436579..23438931-chr3:23441202..23443899,2	K562	blood:
6	chr3:23370714..23373096-chr3:23375354..23377337,2	K562	blood:
7	chr3:23489983..23492292-chr3:23500438..23503341,2	MCF-7	breast:
8	chr3:23483538..23485535-chr3:23501695..23503485,2	K562	blood:
9	chr3:23442881..23445378-chr3:23445759..23448586,2	K562	blood:
10	chr3:23551036..23552990-chr3:23555167..23556922,2	MCF-7	breast:
11	chr3:23375136..23376980-chr3:23383143..23385276,2	MCF-7	breast:
12	chr3:23466052..23468838-chr3:23474911..23476655,2	MCF-7	breast:
13	chr3:23478332..23479926-chr3:23487725..23489400,2	MCF-7	breast:
14	chr3:23413992..23416641-chr3:23420982..23423774,2	MCF-7	breast:
15	chr3:23628866..23630661-chr3:23631573..23633341,2	MCF-7	breast:
16	chr3:23563683..23566443-chr3:23573278..23576217,2	MCF-7	breast:
17	chr3:23576275..23577975-chr3:23583689..23585549,2	K562	blood:
18	chr3:23443862..23447627-chr3:23449749..23452969,4	MCF-7	breast:
19	chr3:23398268..23400293-chr3:23402710..23405112,2	MCF-7	breast:
20	chr3:23447289..23448831-chr3:23450533..23452284,2	K562	blood:
21	chr3:23526588..23528958-chr3:23530661..23532883,2	K562	blood:
22	chr3:23543180..23548543-chr3:23549132..23552642,5	MCF-7	breast:
23	chr3:23370714..23373096-chr3:23375354..23377337,2	K562	blood:
24	chr3:23690692..23692551-chr3:23696388..23698714,2	MCF-7	breast:
25	chr3:23628100..23630491-chr3:23632731..23635658,2	K562	blood:
26	chr3:23466052..23468838-chr3:23474911..23476655,2	MCF-7	breast:
27	chr3:23477379..23479456-chr3:23479836..23482736,2	MCF-7	breast:
28	chr3:23398268..23400293-chr3:23402710..23405112,2	MCF-7	breast:
29	chr3:23690692..23692551-chr3:23696388..23698714,2	MCF-7	breast:
30	chr3:23533666..23536566-chr3:23556700..23559047,2	MCF-7	breast:
31	chr3:23576275..23577975-chr3:23583689..23585549,2	K562	blood:
32	chr3:23442881..23445228-chr3:23445484..23447259,2	K562	blood:
33	chr3:23669289..23670976-chr3:23675177..23676847,2	K562	blood:
34	chr3:23505766..23508563-chr3:23511877..23514869,2	K562	blood:
35	chr3:23506645..23508747-chr3:23509649..23511446,2	MCF-7	breast:
36	chr3:23551036..23552990-chr3:23555167..23556922,2	MCF-7	breast:
37	chr3:23566672..23568510-chr3:23579299..23582210,2	K562	blood:
38	chr3:23689967..23690811-chr3:23841951..23842865,3	MCF-7	breast:
39	chr3:23245352..23245950-chr3:23374735..23375546,2	MCF-7	breast:
40	chr3:23477632..23480027-chr3:23493781..23495810,2	MCF-7	breast:
41	chr3:23628100..23630491-chr3:23632731..23635658,2	K562	blood:
42	chr3:23670081..23672638-chr3:23684312..23686723,2	MCF-7	breast:
43	chr3:23652492..23654408-chr3:23659934..23662555,2	MCF-7	breast:
44	chr3:23483538..23485535-chr3:23501695..23503485,2	K562	blood:
45	chr3:23436371..23438292-chr3:23438375..23440407,2	MCF-7	breast:
46	chr3:23482059..23483566-chr3:23484032..23486053,2	MCF-7	breast:
47	chr3:23506645..23508747-chr3:23509649..23511446,2	MCF-7	breast:
48	chr3:23478332..23479926-chr3:23487725..23489400,2	MCF-7	breast:
49	chr3:23557942..23560310-chr3:23562476..23565287,2	K562	blood:
50	chr3:23442881..23445228-chr3:23445484..23447259,2	K562	blood:

(count:7 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-UBE2E2-1	chr3:23636612-23636741	XLOC_002597
2	lnc-UBE2E2-1	chr3:23634971-23637228	NONHSAT088673
3	lnc-UBE2E2-1	chr3:23643541-23643659	XLOC_002597
4	lnc-NKIRAS1-5	chr3:23431152-23431400	NONHSAT088668
5	lnc-UBE2E2-1	chr3:23636079-23636094	XLOC_002597
6	lnc-UBE2E2-1	chr3:23635941-23636094	XLOC_002597
7	lnc-UBE2E2-1	chr3:23636612-23636774	XLOC_002597

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	UBE2E2	hsa-miR-186-5p	chr3:23631701-23631722

Variant related genes	Relation type
RNU6-788P	TF binding region
ENSG00000221506	TF binding region
RNU6-922P	TF binding region
ENSG00000265645	TF binding region
ENSG00000228171	TF binding region
RNU6-788P	CpG island
ENSG00000221506	CpG island
RNU6-922P	CpG island
ENSG00000265645	CpG island
ENSG00000228171	CpG island
ENSG00000174748	chromatin interactions
ENSG00000197885	chromatin interactions
ENSG00000212269	chromatin interactions
UCK2	miRNA target sites
UBXN2A	miRNA target sites
UCP2	miRNA target sites

Extended variants
information (count: 14069 )
Associated
traits (count: 75 )

Variant overlapped rSNPs/rCNVs (count:14069 , 50 per page) page: 1 2 3 4 5 6 7 ... 282

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs138343286	chr3:23367982-23367983	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs183464316	chr3:23367993-23367994	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs540666843	chr3:23368014-23368015	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs559254125	chr3:23368023-23368024	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs574400224	chr3:23368074-23368075	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs200309171	chr3:23368203-23368204	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs572802712	chr3:23368212-23368213	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs188581492	chr3:23368234-23368235	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs181063841	chr3:23368236-23368237	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs542416646	chr3:23368258-23368259	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs562104275	chr3:23368262-23368263	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs550294095	chr3:23368271-23368272	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs565233042	chr3:23368281-23368282	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs532592469	chr3:23368288-23368289	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs575912429	chr3:23368321-23368322	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs566046255	chr3:23368336-23368337	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs186843190	chr3:23368340-23368341	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs191737765	chr3:23368371-23368372	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs147956539	chr3:23368377-23368378	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs537237892	chr3:23368385-23368386	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs558664229	chr3:23368395-23368396	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs576867213	chr3:23368399-23368400	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs534671148	chr3:23368433-23368434	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs552562803	chr3:23368470-23368471	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs182247579	chr3:23368524-23368525	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs57909730	chr3:23368532-23368533	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs563235419	chr3:23368577-23368578	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs11717397	chr3:23368583-23368584	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs545684225	chr3:23368623-23368624	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs149824399	chr3:23368629-23368630	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs532514737	chr3:23368642-23368643	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs201524331	chr3:23368673-23368674	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs187360040	chr3:23368702-23368703	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs559813286	chr3:23368713-23368714	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs530101664	chr3:23368755-23368756	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs9865602	chr3:23368772-23368773	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs200689270	chr3:23368794-23368795	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs549184240	chr3:23368797-23368798	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs570360320	chr3:23368850-23368851	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs140148987	chr3:23368908-23368909	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs190042140	chr3:23368928-23368929	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs115015521	chr3:23368941-23368942	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs534440334	chr3:23368991-23368992	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs6806387	chr3:23369029-23369030	Weak transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs554573717	chr3:23369032-23369033	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
46	rs567749647	chr3:23369047-23369048	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
47	rs535081398	chr3:23369055-23369056	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
48	rs182318801	chr3:23369075-23369076	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
49	rs185163391	chr3:23369084-23369085	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
50	rs368436816	chr3:23369093-23369094	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:75)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	17603634	CNVD
Neuroblastoma	17327916	CNVD
Glioblastoma multiforme	21080181	CNVD
Neuroblastoma	18923191	CNVD
Colorectal cancer	21297112	CNVD
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
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
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Retinoblastoma	21504564	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
lymphocytic leukemia	21291569	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Renal cell carcinoma	21668985	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Intellectual disability	22102821	CNVD
Esophageal cancer	20955586	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Myelofibrosis	22110671	CNVD
Gastric adenocarcinoma	19115996	CNVD
Squamous cell cancer	20885788	CNVD
Esophageal squamous carcinoma	17470683	CNVD
Breast cancer	17133270	CNVD
Uveal melanoma	20484589	CNVD
Autism	22495311	CNVD
Melanoma	20688739	CNVD
Melanoma	20877625	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:3222 , 50 per page) page: 1 2 3 4 5 6 7 ... 65

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:23357000-23378800	Weak transcription	Brain Angular Gyrus	brain
2	chr3:23363200-23371000	Weak transcription	Skeletal Muscle Female	skeletal muscle
3	chr3:23363800-23371000	Weak transcription	Brain Hippocampus Middle	brain
4	chr3:23365400-23368000	Enhancers	Primary B cells from cord blood	blood
5	chr3:23366000-23368000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
6	chr3:23366200-23371000	Weak transcription	Skeletal Muscle Male	skeletal muscle
7	chr3:23366400-23368000	Enhancers	Primary monocytes fromperipheralblood	blood
8	chr3:23366600-23372600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
9	chr3:23366800-23368000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
10	chr3:23366800-23368000	Enhancers	Primary B cells from peripheral blood	blood
11	chr3:23366800-23368000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
12	chr3:23366800-23368600	Weak transcription	NHLF	lung
13	chr3:23367000-23369000	Weak transcription	Primary hematopoietic stem cells	blood
14	chr3:23367000-23378800	Weak transcription	HSMMtube	muscle
15	chr3:23367200-23371000	Weak transcription	Monocytes-CD14+_RO01746	blood
16	chr3:23367200-23373000	Weak transcription	Brain Substantia Nigra	brain
17	chr3:23367400-23368000	Enhancers	HMEC	breast
18	chr3:23367400-23368000	Enhancers	NHEK	skin
19	chr3:23367400-23368200	Weak transcription	Brain Anterior Caudate	brain
20	chr3:23367400-23371200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
21	chr3:23367400-23391400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
22	chr3:23367600-23368000	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
23	chr3:23367800-23368000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
24	chr3:23367800-23368000	Enhancers	GM12878-XiMat	blood
25	chr3:23368000-23370800	Weak transcription	Primary monocytes fromperipheralblood	blood
26	chr3:23368000-23373000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
27	chr3:23368000-23374400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
28	chr3:23368000-23374600	Weak transcription	NHEK	skin
29	chr3:23368000-23391000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
30	chr3:23369000-23369400	ZNF genes & repeats	Primary hematopoietic stem cells	blood
31	chr3:23369400-23371200	Weak transcription	Primary hematopoietic stem cells	blood
32	chr3:23370800-23372200	Enhancers	Primary monocytes fromperipheralblood	blood
33	chr3:23371000-23371200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
34	chr3:23371000-23371200	Enhancers	Skeletal Muscle Male	skeletal muscle
35	chr3:23371000-23371400	Enhancers	Psoas Muscle	Psoas
36	chr3:23371000-23371400	Enhancers	Skeletal Muscle Female	skeletal muscle
37	chr3:23371000-23372000	Enhancers	Primary neutrophils fromperipheralblood	blood
38	chr3:23371000-23372000	Enhancers	Monocytes-CD14+_RO01746	blood
39	chr3:23371000-23372200	Enhancers	Brain Hippocampus Middle	brain
40	chr3:23371200-23371400	Enhancers	Primary hematopoietic stem cells	blood
41	chr3:23371200-23371600	Enhancers	Primary hematopoietic stem cells short term culture	blood
42	chr3:23371200-23374400	Weak transcription	Skeletal Muscle Male	skeletal muscle
43	chr3:23371400-23372000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
44	chr3:23371400-23372800	Weak transcription	Skeletal Muscle Female	skeletal muscle
45	chr3:23371400-23378400	Weak transcription	Psoas Muscle	Psoas
46	chr3:23372000-23372200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
47	chr3:23372000-23372200	Enhancers	iPS-15b Cell Line	embryonic stem cell
48	chr3:23372000-23372400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
49	chr3:23372000-23382000	Weak transcription	Monocytes-CD14+_RO01746	blood
50	chr3:23372200-23378200	Weak transcription	Brain Hippocampus Middle	brain

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