Variant report

Variant	esv2763960
Chromosome Location	chr6:162542479-163036223
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:162857639-162857816	HepG2	liver:	n/a	n/a
2	ARID3A	chr6:162910482-162910786	HepG2	liver:	n/a	n/a
3	ARID3A	chr6:162794306-162794665	HepG2	liver:	n/a	n/a
4	ARID3A	chr6:162671087-162671724	HepG2	liver:	n/a	n/a
5	ATF1	chr6:162782228-162782581	K562	blood:	n/a	n/a
6	ATF1	chr6:162812215-162812339	K562	blood:	n/a	n/a
7	ATF1	chr6:162784797-162785113	K562	blood:	n/a	n/a
8	ATF1	chr6:162812647-162812847	K562	blood:	n/a	n/a
9	ATF3	chr6:162784742-162785052	K562	blood:	n/a	n/a
10	BACH1	chr6:162975725-162976098	K562	blood:	n/a	n/a
11	BHLHE40	chr6:162599602-162599788	HepG2	liver:	n/a	chr6:162599639-162599660 chr6:162599645-162599654 chr6:162599645-162599654 chr6:162599643-162599656 chr6:162599644-162599653
12	BHLHE40	chr6:162899266-162899534	GM12878	blood:	n/a	n/a
13	BHLHE40	chr6:162578294-162578454	GM12878	blood:	n/a	n/a
14	BHLHE40	chr6:162576834-162576960	GM12878	blood:	n/a	n/a
15	BRCA1	chr6:162658617-162658742	Hela-S3	cervix:	n/a	n/a
16	BRCA1	chr6:162871740-162871751	H1-hESC	embryonic stem cell:	n/a	n/a
17	CBX3	chr6:162784775-162785143	K562	blood:	n/a	n/a
18	CBX3	chr6:162785538-162785848	K562	blood:	n/a	n/a
19	CCNT2	chr6:163001825-163002025	K562	blood:	n/a	n/a
20	CEBPB	chr6:162671554-162671904	HepG2	liver:	n/a	n/a
21	CEBPB	chr6:162871443-162871750	MCF-7	breast:	n/a	chr6:162871605-162871616
22	CEBPB	chr6:162871405-162871712	H1-hESC	embryonic stem cell:	n/a	chr6:162871605-162871616
23	CEBPB	chr6:162599813-162600021	Hela-S3	cervix:	n/a	chr6:162599866-162599877
24	CEBPB	chr6:162910493-162910789	HepG2	liver:	n/a	n/a
25	CEBPB	chr6:162876249-162876534	IMR90	lung:	n/a	n/a
26	CEBPB	chr6:162766353-162766628	IMR90	lung:	n/a	chr6:162766482-162766491 chr6:162766482-162766491 chr6:162766481-162766492 chr6:162766482-162766491 chr6:162766480-162766491 chr6:162766482-162766491 chr6:162766480-162766493
27	CEBPB	chr6:162784873-162785124	H1-hESC	embryonic stem cell:	n/a	chr6:162785029-162785040
28	CEBPB	chr6:162779076-162779247	A549	lung:	n/a	chr6:162779118-162779129
29	CEBPB	chr6:162857299-162857541	HepG2	liver:	n/a	chr6:162857420-162857431
30	CEBPB	chr6:162559772-162560081	HepG2	liver:	n/a	chr6:162559914-162559925
31	CEBPB	chr6:162779025-162779284	HepG2	liver:	n/a	chr6:162779118-162779129
32	CEBPB	chr6:162871496-162871684	HepG2	liver:	n/a	chr6:162871605-162871616
33	CEBPB	chr6:162784761-162785142	K562	blood:	n/a	chr6:162785029-162785040
34	CEBPB	chr6:163036076-163036363	H1-hESC	embryonic stem cell:	n/a	chr6:163036237-163036246 chr6:163036118-163036129 chr6:163036237-163036246 chr6:163036118-163036129 chr6:163036235-163036248 chr6:163036235-163036248 chr6:163036237-163036246 chr6:163036116-163036129 chr6:163036236-163036247
35	CEBPB	chr6:162671584-162671889	IMR90	lung:	n/a	n/a
36	CEBPB	chr6:162568836-162569161	K562	blood:	n/a	chr6:162568989-162568998 chr6:162568989-162568998 chr6:162568989-162568998 chr6:162568987-162569000 chr6:162568988-162568999 chr6:162568987-162569000
37	CEBPB	chr6:162871429-162871791	HepG2	liver:	n/a	chr6:162871605-162871616
38	CEBPB	chr6:162868765-162868950	HepG2	liver:	n/a	chr6:162868884-162868895
39	CEBPB	chr6:162857280-162857594	HepG2	liver:	n/a	chr6:162857420-162857431
40	CEBPB	chr6:162559819-162560075	A549	lung:	n/a	chr6:162559914-162559925
41	CEBPB	chr6:162656289-162656489	A549	lung:	n/a	n/a
42	CEBPB	chr6:162857291-162857590	HepG2	liver:	n/a	chr6:162857420-162857431
43	CEBPB	chr6:162961979-162962215	HepG2	liver:	n/a	chr6:162962080-162962091
44	CEBPB	chr6:162766332-162766577	H1-hESC	embryonic stem cell:	n/a	chr6:162766482-162766491 chr6:162766482-162766491 chr6:162766481-162766492 chr6:162766482-162766491 chr6:162766480-162766491 chr6:162766482-162766491 chr6:162766480-162766493
45	CEBPB	chr6:163036084-163036403	A549	lung:	n/a	chr6:163036237-163036246 chr6:163036118-163036129 chr6:163036237-163036246 chr6:163036118-163036129 chr6:163036235-163036248 chr6:163036235-163036248 chr6:163036237-163036246 chr6:163036116-163036129 chr6:163036236-163036247
46	CEBPB	chr6:162671564-162671902	A549	lung:	n/a	n/a
47	CEBPB	chr6:162896813-162896974	HepG2	liver:	n/a	chr6:162896839-162896850
48	CEBPB	chr6:162910460-162910714	HepG2	liver:	n/a	n/a
49	CEBPB	chr6:162672448-162672478	HepG2	liver:	n/a	n/a
50	CEBPB	chr6:162766327-162766640	HepG2	liver:	n/a	chr6:162766482-162766491 chr6:162766482-162766491 chr6:162766481-162766492 chr6:162766482-162766491 chr6:162766480-162766491 chr6:162766482-162766491 chr6:162766480-162766493

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:162964378-162964428	NHDF-neo	bronchial:	n/a
2	chr6:162865171-162865221	HPAEpiC	pulmonary alveolar:	n/a
3	chr6:162964378-162964428	NHDF-neo	bronchial:	n/a
4	chr6:162865171-162865221	HPAEpiC	pulmonary alveolar:	n/a
5	chr6:162864586-162864636	NB4	blood:	n/a
6	chr6:162683857-162683907	GM12891	blood:	n/a
7	chr6:162864586-162864636	K562	blood:	n/a
8	chr6:162683881-162683931	SK-N-MC	brain:	n/a
9	chr6:162865258-162865308	HRCEpiC	kidney:	n/a
10	chr6:162683961-162684011	GM12891	blood:	n/a
11	chr6:162831837-162831887	NHBE	bronchial:	n/a
12	chr6:162964378-162964428	AG04450	lung:	fetal
13	chr6:162683881-162683931	LNCaP	prostate:	n/a
14	chr6:162865171-162865221	NH-A	brain:	n/a
15	chr6:162684526-162684576	Jurkat	blood:	n/a
16	chr6:162865171-162865221	HCT-116	colon:	n/a
17	chr6:162964378-162964428	HEEpiC	esophagus:	n/a
18	chr6:162865171-162865221	AG04450	lung:	fetal
19	chr6:162683961-162684011	HUVEC	blood vessel:	n/a
20	chr6:162864586-162864636	CMK	blood:	n/a
21	chr6:162831837-162831887	GM12892	blood:	n/a
22	chr6:162964378-162964428	AG10803	skin:	n/a
23	chr6:163024624-163024674	SK-N-SH_RA	brain:	n/a
24	chr6:162683961-162684011	NB4	blood:	n/a
25	chr6:162865258-162865308	IMR90	lung:	fetal
26	chr6:162683857-162683907	Hela-S3	cervix:	n/a
27	chr6:162684526-162684576	AG09319	gingival:	n/a
28	chr6:162865258-162865308	MCF10A-Er-Src	breast:	n/a
29	chr6:162964378-162964428	ovcar-3	ovarian:	n/a
30	chr6:162683857-162683907	K562	blood:	n/a
31	chr6:162684441-162684491	PFSK-1	brain:	n/a
32	chr6:162684441-162684491	HRCEpiC	kidney:	n/a
33	chr6:162863505-162863555	MCF-7	breast:	n/a
34	chr6:162683961-162684011	Jurkat	blood:	n/a
35	chr6:162865258-162865308	RPTEC	kidney:	n/a
36	chr6:162864586-162864636	NHDF-neo	bronchial:	n/a
37	chr6:162863505-162863555	NHBE	bronchial:	n/a
38	chr6:162684441-162684491	BE2_C	brain:	n/a
39	chr6:162683881-162683931	PFSK-1	brain:	n/a
40	chr6:163024624-163024674	MCF10A-Er-Src	breast:	n/a
41	chr6:162684526-162684576	HEK293	kidney:	embryo
42	chr6:162683961-162684011	ovcar-3	ovarian:	n/a
43	chr6:162684526-162684576	A549	lung:	n/a
44	chr6:162684441-162684491	HRPEpiC	eye:	n/a
45	chr6:162683881-162683931	ovcar-3	ovarian:	n/a
46	chr6:162684441-162684491	ProgFib	skin:	n/a
47	chr6:162864586-162864636	ProgFib	skin:	n/a
48	chr6:162684441-162684491	MCF10A-Er-Src	breast:	n/a
49	chr6:162865258-162865308	BJ	skin:	n/a
50	chr6:162684526-162684576	HRE	kidney:	n/a

No.	Distal block	Cell Line	Cell type
1	chr6:162763017..162765353-chr6:162767098..162769301,2	K562	blood:
2	chr6:162666890..162668464-chr6:162670216..162671922,2	K562	blood:
3	chr6:162258059..162258779-chr6:162552660..162553528,2	MCF-7	breast:
4	chr6:162799485..162803733-chr6:162804296..162807777,5	K562	blood:
5	chr6:162553757..162556831-chr6:162558713..162560436,3	K562	blood:
6	chr6:162661286..162663139-chr6:162673530..162675376,2	K562	blood:
7	chr6:162721411..162723925-chr6:162726328..162729326,2	K562	blood:
8	chr6:162661286..162663139-chr6:162673530..162675376,2	K562	blood:
9	chr6:162613600..162615384-chr6:162617227..162618872,2	K562	blood:
10	chr6:162620407..162622935-chr6:162623040..162625617,2	K562	blood:
11	chr6:162960178..162962006-chr6:162962880..162965078,2	K562	blood:
12	chr6:162620407..162622935-chr6:162623040..162625617,2	K562	blood:
13	chr6:163002877..163005708-chr6:163021910..163024946,3	K562	blood:
14	chr6:163002877..163005708-chr6:163021910..163024946,3	K562	blood:
15	chr6:162902802..162905070-chr6:162905406..162907332,2	K562	blood:
16	chr6:162671180..162673472-chr6:162808694..162811227,2	K562	blood:
17	chr6:162643217..162645721-chr6:162646719..162648950,2	K562	blood:
18	chr6:162863367..162864320-chr6:163157771..163158572,4	MCF-7	breast:
19	chr6:162960178..162962006-chr6:162962880..162965078,2	K562	blood:
20	chr6:162768506..162770213-chr6:162786241..162788330,2	K562	blood:
21	chr6:162863816..162864618-chr6:163271757..163272511,2	MCF-7	breast:
22	chr6:162574333..162576032-chr6:162578404..162580150,2	K562	blood:
23	chr6:162721411..162723925-chr6:162726328..162729326,2	K562	blood:
24	chr6:162902802..162905070-chr6:162905406..162907332,2	K562	blood:
25	chr6:162666890..162668464-chr6:162670216..162671922,2	K562	blood:
26	chr6:162552000..162556573-chr6:162556763..162561114,5	K562	blood:
27	chr6:162553757..162556831-chr6:162558713..162560436,3	K562	blood:
28	chr6:162768506..162770213-chr6:162786241..162788330,2	K562	blood:
29	chr6:162671180..162673472-chr6:162808694..162811227,2	K562	blood:
30	chr6:162763017..162765353-chr6:162767098..162769301,2	K562	blood:
31	chr6:162820265..162823089-chr6:162827852..162829559,2	K562	blood:
32	chr6:162613600..162615384-chr6:162617227..162618872,2	K562	blood:
33	chr6:162574333..162576032-chr6:162578404..162580150,2	K562	blood:
34	chr6:162820265..162823089-chr6:162827852..162829559,2	K562	blood:
35	chr6:162799485..162803733-chr6:162804296..162807777,5	K562	blood:
36	chr6:162643217..162645721-chr6:162646719..162648950,2	K562	blood:
37	chr6:162552000..162556573-chr6:162556763..162561114,5	K562	blood:

Variant related genes	Relation type
KRT8P44	TF binding region
KRT8P44	CpG island

Extended variants
information (count: 20406 )
Associated
traits (count: 108 )

Variant overlapped rSNPs/rCNVs (count:20406 , 50 per page) page: 1 2 3 4 5 6 7 ... 409

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs9355981	chr6:162542479-162542480	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs553595894	chr6:162542491-162542492	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs573436178	chr6:162542637-162542638	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs545621976	chr6:162542641-162542642	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs565552479	chr6:162542666-162542667	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs576025711	chr6:162542677-162542678	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs536485402	chr6:162542703-162542704	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs551854583	chr6:162542738-162542739	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs543837857	chr6:162542742-162542743	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs560983919	chr6:162542782-162542783	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs183529308	chr6:162542796-162542797	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs187117589	chr6:162542807-162542808	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs559816975	chr6:162542808-162542809	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs192180866	chr6:162542828-162542829	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs34493917	chr6:162542829-162542830	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs141652811	chr6:162542838-162542839	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs150499361	chr6:162542851-162542852	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs538169641	chr6:162542877-162542878	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs111343379	chr6:162542891-162542892	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs116604799	chr6:162542899-162542900	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs567694193	chr6:162542917-162542918	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs368305995	chr6:162542966-162542967	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs1954921	chr6:162543008-162543009	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs139518744	chr6:162543083-162543084	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs78838724	chr6:162543205-162543206	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
26	rs118022863	chr6:162543304-162543305	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
27	rs6940203	chr6:162543349-162543350	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs535598491	chr6:162543415-162543416	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs80114747	chr6:162543436-162543437	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs544928316	chr6:162543444-162543445	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs182604276	chr6:162543473-162543474	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs574327252	chr6:162543539-162543540	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs12195520	chr6:162543542-162543543	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs539862439	chr6:162543580-162543581	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs559782373	chr6:162543621-162543622	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs532109913	chr6:162543721-162543722	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs551932922	chr6:162543739-162543740	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs377242926	chr6:162543748-162543749	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs112270112	chr6:162543749-162543750	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs71544924	chr6:162543791-162543792	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs562390663	chr6:162543820-162543821	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs539702491	chr6:162543836-162543837	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs531499202	chr6:162543893-162543894	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs187685778	chr6:162543897-162543898	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs191862018	chr6:162543925-162543926	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs182484445	chr6:162543949-162543950	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs547034806	chr6:162543951-162543952	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs566958422	chr6:162543953-162543954	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs539180473	chr6:162543981-162543982	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs187488006	chr6:162543994-162543995	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:108)

Disease	PMID	Source
Uveal melanoma	21693616	CNVD
Glioblastoma multiforme	21080181	CNVD
Biliary cancer	19435499	CNVD
Medulloblastoma	21979893	CNVD
Malaria	21533027	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Ewing''s sarcoma	17952124	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Neuroblastoma	18923191	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Melanoma	18172304	CNVD
Cancer	21637783	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Follicular lymphoma	19010834	CNVD
Non-small cell lung cancer	21044232	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	16608533	CNVD
Non-small cell lung cancer	21385341	CNVD
Prostate cancer	16705090	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Colorectal cancer	16272173	CNVD
Ependymoma	16718352	CNVD
Gastric cancer	17908304	CNVD
High-proliferative meningiomas	17937814	CNVD
Intracranial tumor	16823260	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	16272173	CNVD
Wilms tumour	21544195	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Malignant melanoma	18718029	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Breast cancer	21858162	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	17603634	CNVD
Developmental delay	19490664	CNVD
Burkitt''s lymphoma	18698080	CNVD
Neurodevelopmental disorder	22521361	CNVD
small cell lung cancer	20016488	CNVD
Adenoid cystic carcinoma	18698036	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Leukemia	18688285	CNVD
Renal cell carcinoma	18592004	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Prostate cancer	18632612	CNVD
Lung cancer	18438408	CNVD
Burkitt''s lymphoma	19759907	CNVD
Esophageal cancer	21851588	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Breast cancer	17133270	CNVD
Testicular germ cell tumor	18059402	CNVD
Developmental delay	21147756	CNVD
Chordoma	18071362	CNVD
Myelofibrosis	22110671	CNVD
Autism	22241247	CNVD
Breast cancer	16397240	CNVD
Atherosclerosis	21956041	CNVD
Maculopathy	20981449	CNVD
Retinoblastoma	22278416	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Ovarian cancer	20844748	CNVD
Uveal melanoma	20484589	CNVD
Glioblastoma multiforme	19435819	CNVD
Astrocytoma	16205629	CNVD
Parkinson disease	17160897	CNVD
Cancer	20164920	CNVD
Breast cancer	22522925	CNVD
Schizophrenia	20838587	CNVD
Early-onset parkinson disease	21993715	CNVD
Glioblastoma	18772890	CNVD
Pancreatic cancer	20981101	CNVD
Autism	21360662	CNVD
Melanoma	20877625	CNVD
Pancreatic cancer	17952125	CNVD
Intellectual disability	22102821	CNVD
Parkinson disease	0	CNVD
Cancer	20164919	CNVD
Ovarian cancer	21720365	CNVD
Parkinson disease	21829596	CNVD
Schizophrenia	23813976	CNVD
Gastric cancer	22315472	CNVD
Autism	19404257	CNVD
Schizophrenia	20967226	CNVD
Schizophrenia	21346763	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Attention deficit hyperactivity disorder	19546859	CNVD
Autism	22495309	CNVD
Glioblastoma multiforme	21138945	CNVD
Ovarian cancer	22355333	CNVD
Schizophrenia	19805367	CNVD
Bipolar disorder	19114987	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD

Chromatin state (count:1591 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:162536400-162543200	Weak transcription	Aorta	Aorta
2	chr6:162540200-162543400	Weak transcription	Brain Substantia Nigra	brain
3	chr6:162540800-162543200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
4	chr6:162540800-162543200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
5	chr6:162540800-162543200	Weak transcription	Psoas Muscle	Psoas
6	chr6:162540800-162545800	Weak transcription	Right Atrium	heart
7	chr6:162541000-162545000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
8	chr6:162541200-162545200	Weak transcription	HSMM	muscle
9	chr6:162543200-162543400	ZNF genes & repeats	Aorta	Aorta
10	chr6:162543200-162543400	Enhancers	Psoas Muscle	Psoas
11	chr6:162543200-162543600	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
12	chr6:162543200-162544000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
13	chr6:162543400-162543800	Enhancers	Brain Substantia Nigra	brain
14	chr6:162543800-162545200	Weak transcription	Brain Substantia Nigra	brain
15	chr6:162545000-162545400	Enhancers	Fetal Lung	lung
16	chr6:162545000-162546000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
17	chr6:162545000-162546200	Enhancers	NH-A	brain
18	chr6:162545200-162545600	Enhancers	Brain Substantia Nigra	brain
19	chr6:162545200-162546000	Enhancers	HSMM	muscle
20	chr6:162545800-162546200	Enhancers	Right Atrium	heart
21	chr6:162556600-162556800	Enhancers	Psoas Muscle	Psoas
22	chr6:162557400-162557800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
23	chr6:162560600-162561000	Enhancers	Monocytes-CD14+_RO01746	blood
24	chr6:162560600-162562200	Enhancers	Primary monocytes fromperipheralblood	blood
25	chr6:162560600-162572000	Weak transcription	Skeletal Muscle Male	skeletal muscle
26	chr6:162561000-162561800	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
27	chr6:162561800-162562000	Enhancers	Monocytes-CD14+_RO01746	blood
28	chr6:162562800-162563400	Enhancers	Skeletal Muscle Female	skeletal muscle
29	chr6:162563200-162563400	ZNF genes & repeats	Aorta	Aorta
30	chr6:162563200-162563400	Enhancers	Psoas Muscle	Psoas
31	chr6:162563400-162571400	Weak transcription	Psoas Muscle	Psoas
32	chr6:162563400-162574200	Weak transcription	Aorta	Aorta
33	chr6:162570600-162571000	Enhancers	H1 Cell Line	embryonic stem cell
34	chr6:162570600-162571000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
35	chr6:162570600-162571200	Enhancers	ES-I3 Cell Line	embryonic stem cell
36	chr6:162570600-162571200	Enhancers	iPS-15b Cell Line	embryonic stem cell
37	chr6:162570600-162571400	Enhancers	HUES64 Cell Line	embryonic stem cell
38	chr6:162570600-162571400	Enhancers	iPS-18 Cell Line	embryonic stem cell
39	chr6:162570600-162571400	Enhancers	iPS-20b Cell Line	embryonic stem cell
40	chr6:162570600-162571800	Enhancers	HUES48 Cell Line	embryonic stem cell
41	chr6:162570800-162573600	Enhancers	Primary hematopoietic stem cells short term culture	blood
42	chr6:162571000-162571600	Enhancers	Monocytes-CD14+_RO01746	blood
43	chr6:162571200-162573200	Enhancers	Primary monocytes fromperipheralblood	blood
44	chr6:162571400-162571600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
45	chr6:162571400-162571600	Enhancers	Psoas Muscle	Psoas
46	chr6:162571600-162572000	Weak transcription	Psoas Muscle	Psoas
47	chr6:162571600-162572000	Enhancers	NH-A	brain
48	chr6:162571600-162572600	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
49	chr6:162571600-162572800	Enhancers	HSMMtube	muscle
50	chr6:162571600-162573200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived

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