Variant report

Variant	nsv538212
Chromosome Location	chr6:44925393-45152912
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1030)
CpG islands
(count:183)
Chromatin interactive
region (count:58)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1030 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:45017618-45017640	K562	blood:	n/a	n/a
2	ARID3A	chr6:45151435-45151460	K562	blood:	n/a	n/a
3	ARID3A	chr6:44942228-44942585	K562	blood:	n/a	n/a
4	ARID3A	chr6:45011822-45012263	HepG2	liver:	n/a	n/a
5	ARID3A	chr6:44934203-44935340	K562	blood:	n/a	n/a
6	ARID3A	chr6:45081891-45082077	HepG2	liver:	n/a	n/a
7	ARID3A	chr6:45090824-45091007	HepG2	liver:	n/a	n/a
8	ARID3A	chr6:45017086-45017200	HepG2	liver:	n/a	n/a
9	ARID3A	chr6:45025490-45025613	HepG2	liver:	n/a	n/a
10	ARID3A	chr6:44928633-44929024	HepG2	liver:	n/a	n/a
11	ARID3A	chr6:45152902-45153360	K562	blood:	n/a	n/a
12	ATF1	chr6:45025523-45025589	K562	blood:	n/a	n/a
13	ATF1	chr6:44934477-44934865	K562	blood:	n/a	n/a
14	ATF1	chr6:45123102-45123463	K562	blood:	n/a	n/a
15	ATF1	chr6:45123857-45124210	K562	blood:	n/a	n/a
16	ATF1	chr6:45016978-45017291	K562	blood:	n/a	n/a
17	ATF2	chr6:44966735-44967151	GM12878	blood:	n/a	n/a
18	ATF2	chr6:44966734-44967257	GM12878	blood:	n/a	n/a
19	ATF3	chr6:44934407-44934925	K562	blood:	n/a	n/a
20	BACH1	chr6:44965357-44965412	K562	blood:	n/a	n/a
21	BATF	chr6:44966841-44967148	GM12878	blood:	n/a	n/a
22	BATF	chr6:45139181-45139443	GM12878	blood:	n/a	chr6:45139321-45139331
23	BATF	chr6:45139190-45139394	GM12878	blood:	n/a	chr6:45139321-45139331
24	BATF	chr6:44947204-44947474	GM12878	blood:	n/a	n/a
25	BATF	chr6:44977334-44977648	GM12878	blood:	n/a	chr6:44977540-44977551
26	BATF	chr6:44966783-44967196	GM12878	blood:	n/a	n/a
27	BATF	chr6:45132110-45132459	GM12878	blood:	n/a	n/a
28	BATF	chr6:44977286-44977716	GM12878	blood:	n/a	chr6:44977540-44977551
29	BCL3	chr6:44934546-44934913	K562	blood:	n/a	n/a
30	BCL3	chr6:45132117-45132509	GM12878	blood:	n/a	n/a
31	BHLHE40	chr6:45086708-45086783	K562	blood:	n/a	n/a
32	BHLHE40	chr6:44969459-44969727	GM12878	blood:	n/a	n/a
33	BHLHE40	chr6:44928669-44928955	GM12878	blood:	n/a	n/a
34	BHLHE40	chr6:45131714-45131723	GM12878	blood:	n/a	n/a
35	BHLHE40	chr6:45123836-45124198	GM12878	blood:	n/a	n/a
36	BHLHE40	chr6:45016926-45017297	K562	blood:	n/a	n/a
37	BHLHE40	chr6:44934500-44934832	K562	blood:	n/a	n/a
38	BRCA1	chr6:45011813-45011861	Hela-S3	cervix:	n/a	n/a
39	CBX3	chr6:45132012-45132577	HCT-116	colon:	n/a	n/a
40	CBX3	chr6:45016920-45017304	K562	blood:	n/a	n/a
41	CBX3	chr6:44934371-44934913	HCT-116	colon:	n/a	n/a
42	CBX3	chr6:44940439-44940814	K562	blood:	n/a	n/a
43	CBX3	chr6:44934407-44934915	K562	blood:	n/a	n/a
44	CBX3	chr6:44940388-44940854	K562	blood:	n/a	n/a
45	CBX3	chr6:45109178-45109415	K562	blood:	n/a	n/a
46	CBX3	chr6:44934470-44934850	K562	blood:	n/a	n/a
47	CBX3	chr6:44928552-44929041	HCT-116	colon:	n/a	n/a
48	CBX3	chr6:44934427-44934905	HCT-116	colon:	n/a	n/a
49	CCNT2	chr6:45003117-45003383	K562	blood:	n/a	n/a
50	CCNT2	chr6:44934499-44934885	K562	blood:	n/a	n/a

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:45079679-45079729	HCPEpiC	choroid plexus:	n/a
2	chr6:45143980-45144030	K562	blood:	n/a
3	chr6:45079679-45079729	GM12891	blood:	n/a
4	chr6:45143980-45144030	NHDF-neo	bronchial:	n/a
5	chr6:45079679-45079729	PrEC	prostate:	n/a
6	chr6:45143980-45144030	Jurkat	blood:	n/a
7	chr6:45030454-45030504	K562	blood:	n/a
8	chr6:45143980-45144030	GM12892	blood:	n/a
9	chr6:45030454-45030504	NHBE	bronchial:	n/a
10	chr6:45079679-45079729	RPTEC	kidney:	n/a
11	chr6:45079679-45079729	HEEpiC	esophagus:	n/a
12	chr6:45143980-45144030	AG09309	skin:	n/a
13	chr6:45030454-45030504	Hela-S3	cervix:	n/a
14	chr6:45030454-45030504	BJ	skin:	n/a
15	chr6:45030454-45030504	HUVEC	blood vessel:	n/a
16	chr6:45079679-45079729	HRPEpiC	eye:	n/a
17	chr6:45030454-45030504	HCPEpiC	choroid plexus:	n/a
18	chr6:45030454-45030504	HepG2	liver:	n/a
19	chr6:45030454-45030504	NH-A	brain:	n/a
20	chr6:45030454-45030504	Hepatocyte	liver:	n/a
21	chr6:45143980-45144030	HepG2	liver:	n/a
22	chr6:45079679-45079729	BJ	skin:	n/a
23	chr6:45143980-45144030	ECC-1	luminal epithelium:	n/a
24	chr6:45079679-45079729	Jurkat	blood:	n/a
25	chr6:45079679-45079729	HCF	heart:	n/a
26	chr6:45143980-45144030	HNPCEpiC	eye:	n/a
27	chr6:45143980-45144030	HAEpiC	amniotic membrane:	n/a
28	chr6:45079679-45079729	HPAEpiC	pulmonary alveolar:	n/a
29	chr6:45143980-45144030	PANC-1	pancreas:	n/a
30	chr6:45030454-45030504	HCF	heart:	n/a
31	chr6:45030454-45030504	HEK293	kidney:	embryo
32	chr6:45143980-45144030	RPTEC	kidney:	n/a
33	chr6:45079679-45079729	HL-60	blood:	n/a
34	chr6:45030454-45030504	T-47D	breast:	n/a
35	chr6:45079679-45079729	GM06990	blood:	n/a
36	chr6:45079679-45079729	AG09319	gingival:	n/a
37	chr6:45079679-45079729	BE2_C	brain:	n/a
38	chr6:45079679-45079729	PANC-1	pancreas:	n/a
39	chr6:45143980-45144030	AoSMC	blood vessel:	n/a
40	chr6:45143980-45144030	GM19239	blood:	n/a
41	chr6:45143980-45144030	HRPEpiC	eye:	n/a
42	chr6:45030454-45030504	HRPEpiC	eye:	n/a
43	chr6:45030454-45030504	RPTEC	kidney:	n/a
44	chr6:45030454-45030504	SK-N-MC	brain:	n/a
45	chr6:45079679-45079729	NB4	blood:	n/a
46	chr6:45143980-45144030	A549	lung:	n/a
47	chr6:45030454-45030504	CMK	blood:	n/a
48	chr6:45143980-45144030	IMR90	lung:	fetal
49	chr6:45030454-45030504	PrEC	prostate:	n/a
50	chr6:45030454-45030504	HEEpiC	esophagus:	n/a

(count:58 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr6:45008781..45011238-chr6:45015698..45018079,2	MCF-7	breast:
2	chr6:45008781..45011238-chr6:45015698..45018079,2	MCF-7	breast:
3	chr6:45071425..45074350-chr6:45080859..45082948,2	MCF-7	breast:
4	chr6:45003285..45005012-chr6:45007518..45010080,2	K562	blood:
5	chr6:45091825..45094517-chr6:45344694..45347186,2	MCF-7	breast:
6	chr6:44987589..44991130-chr6:44992558..44996333,3	K562	blood:
7	chr6:44949240..44952197-chr6:44957383..44960219,3	K562	blood:
8	chr6:45049112..45051418-chr6:45052257..45055062,3	K562	blood:
9	chr6:45061664..45064501-chr6:45066770..45068668,2	K562	blood:
10	chr6:45119653..45122627-chr6:45134013..45136661,2	MCF-7	breast:
11	chr6:44949240..44952197-chr6:44957383..44960219,3	K562	blood:
12	chr6:45120420..45122464-chr6:45122631..45125594,2	K562	blood:
13	chr12:48357281..48357866-chr6:45012051..45012551,2	Hela-S3	cervix:
14	chr6:44996729..44999425-chr6:45119837..45121459,2	K562	blood:
15	chr6:44962823..44965402-chr6:44970662..44972612,2	K562	blood:
16	chr6:44963271..44965402-chr6:44968999..44972162,3	K562	blood:
17	chr6:45038976..45040613-chr6:45043879..45046271,2	K562	blood:
18	chr6:45093713..45096382-chr6:45127644..45129447,2	K562	blood:
19	chr6:44972423..44974259-chr6:44978944..44980911,2	K562	blood:
20	chr6:44924333..44926933-chr6:44928218..44930920,2	K562	blood:
21	chr6:45093713..45096382-chr6:45127644..45129447,2	K562	blood:
22	chr6:44987108..44989743-chr6:44993654..44995647,2	K562	blood:
23	chr6:44996729..44999425-chr6:45119837..45121459,2	K562	blood:
24	chr6:44987108..44989743-chr6:44993654..44995647,2	K562	blood:
25	chr6:45071425..45074350-chr6:45080859..45082948,2	MCF-7	breast:
26	chr6:44935484..44938452-chr6:44939240..44940813,2	K562	blood:
27	chr6:45061664..45064501-chr6:45066770..45068668,2	K562	blood:
28	chr6:44963271..44965402-chr6:44968999..44972162,3	K562	blood:
29	chr6:44928658..44930221-chr6:45326668..45328264,2	K562	blood:
30	chr6:45128101..45130973-chr6:45345066..45347922,2	K562	blood:
31	chr6:45092014..45095175-chr6:45095501..45098870,4	K562	blood:
32	chr6:44443174..44444085-chr6:45053756..45054587,2	MCF-7	breast:
33	chr6:45049112..45051418-chr6:45052257..45055062,3	K562	blood:
34	chr6:44917939..44922059-chr6:44925666..44928514,3	K562	blood:
35	chr6:45092014..45095175-chr6:45095501..45098870,4	K562	blood:
36	chr6:44962823..44965402-chr6:44970662..44972612,2	K562	blood:
37	chr6:44924333..44926933-chr6:44928218..44930920,2	K562	blood:
38	chr6:45054220..45054815-chr6:45386791..45387562,3	MCF-7	breast:
39	chr6:44972423..44974259-chr6:44978944..44980911,2	K562	blood:
40	chr6:45083331..45086142-chr6:45155794..45158780,2	K562	blood:
41	chr6:44987589..44991130-chr6:44992558..44996333,3	K562	blood:
42	chr19:27731523..27732363-chr6:45117749..45118249,2	MCF-7	breast:
43	chr6:45038976..45040613-chr6:45043879..45046271,2	K562	blood:
44	chr6:45003285..45005012-chr6:45007518..45010080,2	K562	blood:
45	chr6:44974489..44977160-chr6:44980461..44983338,2	K562	blood:
46	chr6:45126389..45128813-chr6:45129445..45131831,2	K562	blood:
47	chr6:45124236..45126557-chr6:45137066..45139205,2	MCF-7	breast:
48	chr6:45117043..45119503-chr6:45122120..45124121,2	K562	blood:
49	chr6:45120420..45122464-chr6:45122631..45125594,2	K562	blood:
50	chr6:45138020..45139823-chr6:45139972..45141878,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RUNX2-4	chr6:45126607-45127248	NONHSAT112972

No data

Variant related genes	Relation type
SUPT3H	TF binding region
ENSG00000219384	TF binding region
SUPT3H	CpG island
ENSG00000219384	CpG island
ENSG00000219384	chromatin interactions
ENSG00000134291	chromatin interactions
ENSG00000196284	chromatin interactions

Extended variants
information (count: 7634 )
Associated
traits (count: 100 )

Variant overlapped rSNPs/rCNVs (count:7634 , 50 per page) page: 1 2 3 4 5 6 7 ... 153

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs111577607	chr6:44925409-44925410	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs150750371	chr6:44925411-44925412	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs115778690	chr6:44925426-44925427	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs137963567	chr6:44925432-44925433	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs544520421	chr6:44925440-44925441	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs191498826	chr6:44925444-44925445	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs550730581	chr6:44925479-44925480	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs199771399	chr6:44925505-44925506	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs73735273	chr6:44925550-44925551	Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs542398519	chr6:44925563-44925564	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs183290851	chr6:44925583-44925584	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs564286	chr6:44925662-44925663	Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs367562818	chr6:44925668-44925669	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs558278240	chr6:44925706-44925707	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs592240	chr6:44925736-44925737	Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs188789161	chr6:44925773-44925774	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs190797564	chr6:44925776-44925777	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs183451309	chr6:44925819-44925820	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs3799987	chr6:44925834-44925835	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
20	rs3799988	chr6:44925848-44925849	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs147147035	chr6:44925861-44925862	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs114500922	chr6:44925884-44925885	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs186627796	chr6:44925927-44925928	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs558593730	chr6:44925930-44925931	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs570515129	chr6:44925931-44925932	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs538198489	chr6:44926031-44926032	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs556622764	chr6:44926123-44926124	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs575074002	chr6:44926133-44926134	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs555353649	chr6:44926137-44926138	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs191135746	chr6:44926139-44926140	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs554389493	chr6:44926141-44926142	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs572639064	chr6:44926166-44926167	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs540349077	chr6:44926174-44926175	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs564929723	chr6:44926211-44926212	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs10948188	chr6:44926212-44926213	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
36	rs544187522	chr6:44926235-44926236	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs12212190	chr6:44926271-44926272	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
38	rs376587473	chr6:44926280-44926281	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs34240217	chr6:44926317-44926318	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs144965278	chr6:44926319-44926320	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs369901439	chr6:44926323-44926324	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs371008478	chr6:44926352-44926353	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs182875717	chr6:44926353-44926354	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs9472409	chr6:44926431-44926432	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
45	rs570602861	chr6:44926437-44926438	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs144817945	chr6:44926451-44926452	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs550125550	chr6:44926463-44926464	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs61444470	chr6:44926472-44926473	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs546593204	chr6:44926502-44926503	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs549424324	chr6:44926520-44926521	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:100)

Disease	PMID	Source
Follicular lymphoma	20505157	CNVD
Glioblastoma multiforme	21080181	CNVD
Ewing''s sarcoma	21437220	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Leukemia	21518781	CNVD
Cancer	21637783	CNVD
Facial dysmorphism	22105932	CNVD
Medulloblastoma	21979893	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Endometrial cancer	22040021	CNVD
Acute myeloid leukemia	16864856	CNVD
Breast cancer	21264507	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	16751803	CNVD
Bladder cancer	19088036	CNVD
Wilms tumour	21544195	CNVD
Uveal melanoma	21693616	CNVD
Biliary cancer	19435499	CNVD
Malaria	21533027	CNVD
Retinoblastoma	19183342	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21858162	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	21448237	CNVD
Melanoma	18172304	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Hepatocellular carcinoma	16750200	CNVD
Autism	22495311	CNVD
Cancer	16790693	CNVD
Cervical cancer	21062161	CNVD
Systemic lupus erythematosus	17503323	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Urothelial carcinoma	18382360	CNVD
Cancer	21183584	CNVD
Hodgkin''s lymphoma	17606441	CNVD
small cell lung cancer	20016488	CNVD
Gastric cancer	17908304	CNVD
Metanephric adenoma	20802469	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Neuroblastoma	16790693	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Cleidocranial dysplasia	18696259	CNVD
Holoprosencephaly	21359414	CNVD
Liposarcoma	21253554	CNVD
Uveal melanoma	20484589	CNVD
Fibroblasts	20926602	CNVD
Osteosarcoma	16790693	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
Lung cancer	18438408	CNVD
Ovarian cancer	21720365	CNVD
Osteosarcoma	21197465	CNVD
Gastric cancer	24379144	CNVD
Neuroblastoma	18923191	CNVD
abnormal development	18461090	CNVD
Breast cancer	17603634	CNVD
Breast cancer	21364760	CNVD
Colorectal cancer	16790693	CNVD
Congenital adrenal hyperplasia	18478071	CNVD
Congenital anomalies of the kidney and urinary tract	18316590	CNVD
Systemic lupus erythematosus	19287148	CNVD
Colorectal cancer	19359472	CNVD
Multiple myeloma	16616336	CNVD
Chordoma	18071362	CNVD
Follicular lymphoma	16790693	CNVD
Osteosarcoma	19286668	CNVD
Neurocytoma	17123091	CNVD
Myelofibrosis	22110671	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Ovarian cancer	20844748	CNVD
lymphocytic leukemia	21291569	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Pancreatic cancer	17952125	CNVD
Bipolar disorder	19114987	CNVD
Schizophrenia	23813976	CNVD

Chromatin state (count:986 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:44913400-44930000	Weak transcription	Pancreas	Pancrea
2	chr6:44913600-44928600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
3	chr6:44915400-44932800	Weak transcription	Left Ventricle	heart
4	chr6:44918000-44926600	Weak transcription	Esophagus	oesophagus
5	chr6:44918000-44928400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
6	chr6:44918200-44928400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
7	chr6:44919600-44925400	Weak transcription	Ovary	ovary
8	chr6:44919600-44927600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
9	chr6:44919600-44943200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
10	chr6:44919800-44928600	Weak transcription	HepG2	liver
11	chr6:44920600-44937600	Weak transcription	Primary hematopoietic stem cells	blood
12	chr6:44923400-44935000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
13	chr6:44923600-44926200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
14	chr6:44926200-44926400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
15	chr6:44927400-44930400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
16	chr6:44928400-44928800	Enhancers	Muscle Satellite Cultured Cells	--
17	chr6:44928400-44929000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
18	chr6:44928400-44929200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
19	chr6:44928400-44930800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
20	chr6:44928600-44929000	Enhancers	GM12878-XiMat	blood
21	chr6:44928600-44929000	Enhancers	NHDF-Ad	bronchial
22	chr6:44928600-44929000	Enhancers	NHLF	lung
23	chr6:44928600-44929200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
24	chr6:44928600-44929200	Enhancers	HepG2	liver
25	chr6:44928800-44929200	Weak transcription	Primary B cells from cord blood	blood
26	chr6:44928800-44933800	Weak transcription	Muscle Satellite Cultured Cells	--
27	chr6:44929000-44933800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
28	chr6:44929200-44933800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
29	chr6:44929200-44934600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
30	chr6:44930400-44932400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
31	chr6:44930800-44934200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
32	chr6:44932400-44933800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
33	chr6:44932800-44933000	Enhancers	Left Ventricle	heart
34	chr6:44933400-44933800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
35	chr6:44933600-44933800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
36	chr6:44933600-44934000	Enhancers	Primary T killer naive cells fromperipheralblood	blood
37	chr6:44933600-44934800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
38	chr6:44933600-44934800	Enhancers	Brain Hippocampus Middle	brain
39	chr6:44933600-44935400	Enhancers	NH-A	brain
40	chr6:44933600-44935400	Enhancers	NHEK	skin
41	chr6:44933600-44937800	Enhancers	Fetal Heart	heart
42	chr6:44933800-44934000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
43	chr6:44933800-44934600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
44	chr6:44933800-44934600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
45	chr6:44933800-44934600	Enhancers	Hela-S3	cervix
46	chr6:44933800-44935400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
47	chr6:44933800-44935400	Enhancers	Muscle Satellite Cultured Cells	--
48	chr6:44933800-44935800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
49	chr6:44934000-44934400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
50	chr6:44934000-44939800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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