Variant report

Variant	nsv481981
Chromosome Location	chr6:161829077-162215745
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2661)
CpG islands
(count:1712)
Chromatin interactive
region (count:98)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2661 , 50 per page) page: 1 2 3 4 5 6 7 ... 54

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:162005585-162005674	K562	blood:	n/a	n/a
2	ARID3A	chr6:161852467-161852474	K562	blood:	n/a	n/a
3	ATF1	chr6:161971326-161971631	K562	blood:	n/a	n/a
4	ATF1	chr6:162004714-162004819	K562	blood:	n/a	n/a
5	ATF1	chr6:161999566-161999833	K562	blood:	n/a	n/a
6	ATF1	chr6:162140696-162140749	K562	blood:	n/a	n/a
7	ATF1	chr6:161860090-161860611	K562	blood:	n/a	n/a
8	ATF1	chr6:162206880-162206984	K562	blood:	n/a	n/a
9	ATF1	chr6:161954475-161954797	K562	blood:	n/a	n/a
10	ATF1	chr6:162131444-162131661	K562	blood:	n/a	n/a
11	ATF1	chr6:161955575-161955847	K562	blood:	n/a	n/a
12	ATF1	chr6:162132283-162132287	K562	blood:	n/a	n/a
13	ATF1	chr6:161865538-161865833	K562	blood:	n/a	n/a
14	ATF2	chr6:161964957-161965386	GM12878	blood:	n/a	n/a
15	ATF2	chr6:161957239-161957535	GM12878	blood:	n/a	n/a
16	ATF3	chr6:161971276-161971680	K562	blood:	n/a	n/a
17	ATF3	chr6:161860005-161860389	K562	blood:	n/a	n/a
18	ATF3	chr6:161860142-161860371	K562	blood:	n/a	n/a
19	ATF3	chr6:162040045-162040462	K562	blood:	n/a	n/a
20	BACH1	chr6:162051173-162051178	K562	blood:	n/a	n/a
21	BACH1	chr6:162062267-162062596	H1-hESC	embryonic stem cell:	n/a	n/a
22	BACH1	chr6:162053102-162053295	H1-hESC	embryonic stem cell:	n/a	chr6:162053163-162053177
23	BACH1	chr6:162104075-162104373	H1-hESC	embryonic stem cell:	n/a	n/a
24	BACH1	chr6:161839504-161839725	H1-hESC	embryonic stem cell:	n/a	n/a
25	BATF	chr6:161965025-161965281	GM12878	blood:	n/a	chr6:161965148-161965158 chr6:161965147-161965158
26	BATF	chr6:161939758-161939960	GM12878	blood:	n/a	chr6:161939861-161939872
27	BATF	chr6:162161546-162161747	GM12878	blood:	n/a	n/a
28	BATF	chr6:161965002-161965288	GM12878	blood:	n/a	chr6:161965148-161965158 chr6:161965147-161965158
29	BCL11A	chr6:162148231-162148386	H1-hESC	embryonic stem cell:	n/a	n/a
30	BCL3	chr6:161833358-161834046	GM12878	blood:	n/a	n/a
31	BCL3	chr6:161833444-161833985	GM12878	blood:	n/a	n/a
32	BCL3	chr6:161832620-161832893	GM12878	blood:	n/a	n/a
33	BCL3	chr6:161832537-161832911	GM12878	blood:	n/a	n/a
34	BCL3	chr6:162184127-162184365	GM12878	blood:	n/a	n/a
35	BCL3	chr6:162184122-162184349	GM12878	blood:	n/a	n/a
36	BHLHE40	chr6:161836360-161836625	K562	blood:	n/a	n/a
37	BHLHE40	chr6:161860021-161860772	K562	blood:	n/a	n/a
38	BHLHE40	chr6:162164901-162165154	GM12878	blood:	n/a	n/a
39	BHLHE40	chr6:161865581-161865839	K562	blood:	n/a	n/a
40	CBX3	chr6:161954377-161954650	K562	blood:	n/a	n/a
41	CBX3	chr6:161832226-161832544	K562	blood:	n/a	n/a
42	CBX3	chr6:161832165-161832599	K562	blood:	n/a	n/a
43	CBX3	chr6:161865525-161865845	K562	blood:	n/a	n/a
44	CCNT2	chr6:161860175-161860516	K562	blood:	n/a	n/a
45	CEBPB	chr6:162004561-162004927	HepG2	liver:	n/a	chr6:162004733-162004744
46	CEBPB	chr6:162073884-162074194	A549	lung:	n/a	n/a
47	CEBPB	chr6:161919461-161919792	H1-hESC	embryonic stem cell:	n/a	n/a
48	CEBPB	chr6:162039972-162040478	A549	lung:	n/a	chr6:162040293-162040304 chr6:162040292-162040305
49	CEBPB	chr6:162157945-162158265	H1-hESC	embryonic stem cell:	n/a	chr6:162158110-162158121
50	CEBPB	chr6:161971294-161971642	K562	blood:	n/a	n/a

(count:1712 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:162068382-162068432	BE2_C	brain:	n/a
2	chr6:162067177-162067227	SK-N-SH_RA	brain:	n/a
3	chr6:161863721-161863771	SKMC	muscle:	n/a
4	chr6:162065571-162065621	HPAEpiC	pulmonary alveolar:	n/a
5	chr6:162068382-162068432	BE2_C	brain:	n/a
6	chr6:162067177-162067227	SK-N-SH_RA	brain:	n/a
7	chr6:161863721-161863771	SKMC	muscle:	n/a
8	chr6:162065571-162065621	HPAEpiC	pulmonary alveolar:	n/a
9	chr6:161995369-161995419	MCF-7	breast:	n/a
10	chr6:161836665-161836715	NH-A	brain:	n/a
11	chr6:162067688-162067738	T-47D	breast:	n/a
12	chr6:161995302-161995352	Caco-2	colon:	n/a
13	chr6:161864557-161864607	Hela-S3	cervix:	n/a
14	chr6:161837218-161837268	ECC-1	luminal epithelium:	n/a
15	chr6:161860635-161860685	BE2_C	brain:	n/a
16	chr6:162066927-162066977	HL-60	blood:	n/a
17	chr6:161837387-161837437	NT2-D1	testis:	n/a
18	chr6:161995302-161995352	SKMC	muscle:	n/a
19	chr6:161863721-161863771	ProgFib	skin:	n/a
20	chr6:161836665-161836715	MCF-7	breast:	n/a
21	chr6:161836946-161836996	H1-hESC	embryonic stem cell:	embryo
22	chr6:161860203-161860253	GM19239	blood:	n/a
23	chr6:161836525-161836575	HCPEpiC	choroid plexus:	n/a
24	chr6:161836946-161836996	HL-60	blood:	n/a
25	chr6:162066927-162066977	MCF-7	breast:	n/a
26	chr6:162071140-162071190	AG09309	skin:	n/a
27	chr6:162071140-162071190	GM12892	blood:	n/a
28	chr6:161836665-161836715	SK-N-MC	brain:	n/a
29	chr6:161995337-161995387	GM19239	blood:	n/a
30	chr6:162068382-162068432	HCPEpiC	choroid plexus:	n/a
31	chr6:162060886-162060936	MCF-7	breast:	n/a
32	chr6:161864557-161864607	HRE	kidney:	n/a
33	chr6:162064339-162064389	HUVEC	blood vessel:	n/a
34	chr6:161860359-161860409	AoSMC	blood vessel:	n/a
35	chr6:161860359-161860409	AG09319	gingival:	n/a
36	chr6:162068382-162068432	PFSK-1	brain:	n/a
37	chr6:161863721-161863771	PANC-1	pancreas:	n/a
38	chr6:162066927-162066977	MCF10A-Er-Src	breast:	n/a
39	chr6:162064339-162064389	HCF	heart:	n/a
40	chr6:161864488-161864538	AG04449	skin:	fetal
41	chr6:162064339-162064389	ProgFib	skin:	n/a
42	chr6:161864557-161864607	CMK	blood:	n/a
43	chr6:161863721-161863771	MCF10A-Er-Src	breast:	n/a
44	chr6:161995369-161995419	SK-N-SH	brain:	n/a
45	chr6:161837218-161837268	Caco-2	colon:	n/a
46	chr6:161836946-161836996	LNCaP	prostate:	n/a
47	chr6:161836946-161836996	MCF10A-Er-Src	breast:	n/a
48	chr6:161836525-161836575	GM12891	blood:	n/a
49	chr6:162067688-162067738	Caco-2	colon:	n/a
50	chr6:161860263-161860313	BE2_C	brain:	n/a

(count:98 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr6:162000857..162002528-chr6:162026039..162027693,2	K562	blood:
2	chr6:162057469..162059362-chr6:162068678..162070292,2	K562	blood:
3	chr6:161855223..161857273-chr6:161905432..161907491,2	MCF-7	breast:
4	chr6:162135808..162138276-chr6:162142475..162145172,2	K562	blood:
5	chr6:162041107..162043997-chr6:162053743..162055556,2	K562	blood:
6	chr6:162212614..162214396-chr6:162214709..162217609,2	MCF-7	breast:
7	chr6:162064140..162064803-chr7:123198816..123199394,2	MCF-7	breast:
8	chr6:161839408..161840069-chr6:161919484..161920171,3	K562	blood:
9	chr6:161827499..161830369-chr6:161855859..161857703,2	MCF-7	breast:
10	chr6:161848154..161849846-chr6:161859403..161861110,2	MCF-7	breast:
11	chr6:161848154..161849846-chr6:161859403..161861110,2	MCF-7	breast:
12	chr6:161850736..161851659-chr6:161919208..161919887,3	K562	blood:
13	chr6:161859122..161861758-chr6:161866811..161869668,2	MCF-7	breast:
14	chr6:161845580..161847353-chr6:161848998..161851271,2	MCF-7	breast:
15	chr6:161860070..161861572-chr6:161862140..161863792,2	MCF-7	breast:
16	chr6:162039551..162040468-chr6:162115665..162116674,7	MCF-7	breast:
17	chr6:162075282..162077598-chr6:162078551..162080758,2	K562	blood:
18	chr6:161962166..161963929-chr6:161965968..161968206,2	K562	blood:
19	chr6:161845580..161847353-chr6:161848998..161851271,2	MCF-7	breast:
20	chr6:162000857..162002528-chr6:162026039..162027693,2	K562	blood:
21	chr5:153090609..153093589-chr6:161855798..161858427,3	MCF-7	breast:
22	chr6:161966825..161970007-chr6:161974073..161976606,3	K562	blood:
23	chr6:162211723..162213448-chr6:162215614..162217575,2	K562	blood:
24	chr6:161855223..161857273-chr6:161905432..161907491,2	MCF-7	breast:
25	chr6:162211723..162213448-chr6:162215614..162217575,2	K562	blood:
26	chr6:161839144..161840001-chr6:161919199..161919993,2	MCF-7	breast:
27	chr6:162052847..162055292-chr6:162059575..162062461,2	MCF-7	breast:
28	chr6:161920614..161923541-chr6:161940128..161942185,2	K562	blood:
29	chr6:162052847..162055292-chr6:162059575..162062461,2	MCF-7	breast:
30	chr6:161859122..161861758-chr6:161866811..161869668,2	MCF-7	breast:
31	chr6:161827498..161831035-chr6:161833776..161838096,4	K562	blood:
32	chr6:161826891..161829319-chr6:161893488..161895593,2	K562	blood:
33	chr6:161827499..161830369-chr6:161855859..161857703,2	MCF-7	breast:
34	chr6:161855024..161858360-chr6:161858723..161860898,4	MCF-7	breast:
35	chr6:161864849..161867369-chr6:162020785..162023410,2	K562	blood:
36	chr6:161850853..161851797-chr6:161918921..161919717,2	MCF-7	breast:
37	chr6:162041107..162043997-chr6:162053743..162055556,2	K562	blood:
38	chr6:161850853..161851797-chr6:161918921..161919717,2	MCF-7	breast:
39	chr6:161814672..161815385-chr6:161919205..161920148,2	MCF-7	breast:
40	chr19:35885081..35886581-chr6:162062521..162064392,2	K562	blood:
41	chr6:162001523..162004451-chr6:162007412..162009361,2	K562	blood:
42	chr6:162057469..162059362-chr6:162068678..162070292,2	K562	blood:
43	chr6:162111336..162114011-chr6:162137192..162139483,2	K562	blood:
44	chr6:161836595..161839567-chr6:161842900..161844597,2	K562	blood:
45	chr6:162056640..162058918-chr6:162062226..162064429,2	K562	blood:
46	chr6:162075282..162077598-chr6:162078551..162080758,2	K562	blood:
47	chr6:161831270..161834160-chr6:161834412..161837720,3	K562	blood:
48	chr6:161850736..161851659-chr6:161919208..161919887,3	K562	blood:
49	chr6:161874908..161877099-chr6:161907040..161908685,2	K562	blood:
50	chr6:161948248..161953523-chr6:161953771..161956538,5	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AGPAT4-2	chr6:161984667-161986399	NONHSAT115940

No data

Variant related genes	Relation type
ENSG00000221021	TF binding region
ENSG00000221021	CpG island
ENSG00000196542	chromatin interactions

Extended variants
information (count: 14334 )
Associated
traits (count: 98 )

Variant overlapped rSNPs/rCNVs (count:14334 , 50 per page) page: 1 2 3 4 5 6 7 ... 287

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs192181937	chr6:161829099-161829100	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
2	rs571041933	chr6:161829132-161829133	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs565133229	chr6:161829152-161829153	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs138349963	chr6:161829156-161829157	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs370646620	chr6:161829208-161829209	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs16892499	chr6:161829209-161829210	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs547536336	chr6:161829213-161829214	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs536503579	chr6:161829277-161829278	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs553643448	chr6:161829294-161829295	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs570763156	chr6:161829307-161829308	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs567050507	chr6:161829309-161829310	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs539271177	chr6:161829311-161829312	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs575958373	chr6:161829350-161829351	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs35131999	chr6:161829366-161829367	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs568986859	chr6:161829367-161829368	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs559085098	chr6:161829410-161829411	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs575854773	chr6:161829420-161829421	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs10945750	chr6:161829428-161829429	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
19	rs11964719	chr6:161829457-161829458	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs200376387	chr6:161829475-161829476	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs184347040	chr6:161829489-161829490	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs11313718	chr6:161829515-161829516	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs564235807	chr6:161829529-161829530	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs77742136	chr6:161829532-161829533	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs149294333	chr6:161829564-161829565	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs559624926	chr6:161829582-161829583	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs190468567	chr6:161829712-161829713	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs4708906	chr6:161829724-161829725	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs564632792	chr6:161829804-161829805	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs115850312	chr6:161829819-161829820	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs370233593	chr6:161829864-161829865	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs144571251	chr6:161829876-161829877	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs117921853	chr6:161829877-161829878	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs529712944	chr6:161829886-161829887	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs546963685	chr6:161829897-161829898	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs60815343	chr6:161829943-161829944	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs368743748	chr6:161830027-161830028	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs535576814	chr6:161830044-161830045	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs148058876	chr6:161830087-161830088	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs368178350	chr6:161830145-161830146	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs141760738	chr6:161830178-161830179	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs569485835	chr6:161830213-161830214	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs537920582	chr6:161830217-161830218	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs182240816	chr6:161830218-161830219	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs60847850	chr6:161830226-161830227	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs534230206	chr6:161830236-161830237	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs147220893	chr6:161830271-161830272	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs140259093	chr6:161830272-161830273	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs144224583	chr6:161830314-161830315	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs187128528	chr6:161830357-161830358	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:98)

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
Non-syndromic sensorineural hearing loss	22037309	CNVD
Cancer	20164919	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Bipolar disorder	19114987	CNVD
Ovarian cancer	21720365	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Schizophrenia	20967226	CNVD

Chromatin state (count:1921 , 50 per page) page: 1 2 3 4 5 6 7 ... 39

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:161780600-161835800	Weak transcription	Right Atrium	heart
2	chr6:161821800-161834000	Weak transcription	Fetal Muscle Trunk	muscle
3	chr6:161826800-161829200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr6:161826800-161829200	Enhancers	HMEC	breast
5	chr6:161826800-161829400	Enhancers	NHDF-Ad	bronchial
6	chr6:161826800-161829400	Enhancers	NHLF	lung
7	chr6:161826800-161831000	Enhancers	Muscle Satellite Cultured Cells	--
8	chr6:161827000-161829800	Enhancers	HSMMtube	muscle
9	chr6:161827400-161829200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
10	chr6:161827400-161829200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
11	chr6:161827400-161829200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
12	chr6:161827400-161829400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
13	chr6:161827400-161829400	Enhancers	NH-A	brain
14	chr6:161827400-161829400	Enhancers	Osteobl	bone
15	chr6:161827600-161829200	Enhancers	GM12878-XiMat	blood
16	chr6:161827600-161829800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
17	chr6:161827600-161829800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
18	chr6:161827600-161829800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
19	chr6:161827600-161831400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
20	chr6:161827600-161831400	Enhancers	Fetal Muscle Leg	muscle
21	chr6:161827800-161829200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
22	chr6:161827800-161829200	Enhancers	Skeletal Muscle Male	skeletal muscle
23	chr6:161827800-161829600	Weak transcription	A549	lung
24	chr6:161828400-161829400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
25	chr6:161828600-161830400	Weak transcription	Fetal Brain Male	brain
26	chr6:161828600-161831200	Enhancers	HSMM	muscle
27	chr6:161828800-161830400	Weak transcription	Brain Substantia Nigra	brain
28	chr6:161828800-161830400	Weak transcription	Skeletal Muscle Female	skeletal muscle
29	chr6:161828800-161834000	Weak transcription	Psoas Muscle	Psoas
30	chr6:161828800-161834200	Weak transcription	Brain Anterior Caudate	brain
31	chr6:161829000-161829200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
32	chr6:161829000-161829200	Flanking Active TSS	K562	blood
33	chr6:161829000-161832600	Weak transcription	Pancreas	Pancrea
34	chr6:161829200-161829600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
35	chr6:161829200-161830000	Enhancers	K562	blood
36	chr6:161829200-161830200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
37	chr6:161829200-161830400	Weak transcription	Skeletal Muscle Male	skeletal muscle
38	chr6:161829200-161830600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
39	chr6:161829200-161831000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
40	chr6:161829400-161830200	Weak transcription	NHDF-Ad	bronchial
41	chr6:161829400-161830400	Weak transcription	NHLF	lung
42	chr6:161829400-161831000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
43	chr6:161829600-161829800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
44	chr6:161829600-161829800	Enhancers	A549	lung
45	chr6:161829800-161831000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
46	chr6:161829800-161834000	Weak transcription	HSMMtube	muscle
47	chr6:161830000-161830600	Weak transcription	K562	blood
48	chr6:161830200-161830400	Enhancers	NHDF-Ad	bronchial
49	chr6:161830200-161830800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
50	chr6:161830400-161830600	Enhancers	Brain Substantia Nigra	brain

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