Variant report

Variant	esv1813536
Chromosome Location	chr6:34455242-34545123
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2021)
CpG islands
(count:2749)
Chromatin interactive
region (count:192)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2021 , 50 per page) page: 1 2 3 4 5 6 7 ... 41

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:34494959-34495288	HepG2	liver:	n/a	n/a
2	ARID3A	chr6:34535143-34535361	HepG2	liver:	n/a	n/a
3	ARID3A	chr6:34494652-34494762	K562	blood:	n/a	n/a
4	ARID3A	chr6:34485472-34485719	K562	blood:	n/a	n/a
5	ARID3A	chr6:34537168-34537342	K562	blood:	n/a	n/a
6	ARID3A	chr6:34528420-34528567	HepG2	liver:	n/a	n/a
7	ARID3A	chr6:34495041-34495171	K562	blood:	n/a	n/a
8	ARID3A	chr6:34530717-34531006	K562	blood:	n/a	n/a
9	ARID3A	chr6:34528321-34529035	K562	blood:	n/a	n/a
10	ATF1	chr6:34530640-34531020	K562	blood:	n/a	n/a
11	ATF1	chr6:34498693-34498808	K562	blood:	n/a	n/a
12	ATF1	chr6:34528256-34528770	K562	blood:	n/a	n/a
13	ATF2	chr6:34494984-34495307	H1-hESC	embryonic stem cell:	n/a	n/a
14	ATF3	chr6:34458829-34459117	K562	blood:	n/a	n/a
15	ATF3	chr6:34485205-34485489	K562	blood:	n/a	n/a
16	BACH1	chr6:34494673-34494811	K562	blood:	n/a	n/a
17	BACH1	chr6:34458877-34459076	K562	blood:	n/a	n/a
18	BACH1	chr6:34525098-34525122	K562	blood:	n/a	n/a
19	BACH1	chr6:34458837-34459209	H1-hESC	embryonic stem cell:	n/a	n/a
20	BACH1	chr6:34528081-34528565	K562	blood:	n/a	n/a
21	BCL3	chr6:34543140-34543668	K562	blood:	n/a	chr6:34543350-34543359
22	BCL3	chr6:34522720-34523036	GM12878	blood:	n/a	n/a
23	BCL3	chr6:34522693-34523062	GM12878	blood:	n/a	n/a
24	BCL3	chr6:34541372-34541610	GM12878	blood:	n/a	n/a
25	BCL3	chr6:34463889-34464156	GM12878	blood:	n/a	n/a
26	BCLAF1	chr6:34494974-34495328	GM12878	blood:	n/a	n/a
27	BHLHE40	chr6:34525097-34525230	K562	blood:	n/a	n/a
28	BHLHE40	chr6:34535821-34536274	HepG2	liver:	n/a	n/a
29	BHLHE40	chr6:34512632-34512964	K562	blood:	n/a	n/a
30	BHLHE40	chr6:34531305-34531454	K562	blood:	n/a	n/a
31	BHLHE40	chr6:34458903-34459141	K562	blood:	n/a	n/a
32	BHLHE40	chr6:34495040-34495240	GM12878	blood:	n/a	n/a
33	BHLHE40	chr6:34481627-34482576	K562	blood:	n/a	n/a
34	BHLHE40	chr6:34535812-34536294	K562	blood:	n/a	n/a
35	BHLHE40	chr6:34526077-34526348	K562	blood:	n/a	n/a
36	BHLHE40	chr6:34494998-34495331	K562	blood:	n/a	n/a
37	BHLHE40	chr6:34530292-34531071	K562	blood:	n/a	n/a
38	BHLHE40	chr6:34528358-34529016	HepG2	liver:	n/a	n/a
39	BHLHE40	chr6:34527683-34529135	K562	blood:	n/a	n/a
40	BHLHE40	chr6:34498559-34498914	K562	blood:	n/a	n/a
41	BRCA1	chr6:34534813-34534889	H1-hESC	embryonic stem cell:	n/a	n/a
42	BRCA1	chr6:34459183-34459214	HepG2	liver:	n/a	n/a
43	BRCA1	chr6:34528656-34528787	HepG2	liver:	n/a	n/a
44	BRCA1	chr6:34528383-34528433	HepG2	liver:	n/a	n/a
45	BRCA1	chr6:34495129-34495249	GM12878	blood:	n/a	n/a
46	BRCA1	chr6:34458193-34458291	HepG2	liver:	n/a	n/a
47	BRCA1	chr6:34495142-34495167	HepG2	liver:	n/a	n/a
48	BRCA1	chr6:34539475-34539630	HepG2	liver:	n/a	n/a
49	CBX3	chr6:34530537-34531593	K562	blood:	n/a	n/a
50	CBX3	chr6:34504717-34505022	K562	blood:	n/a	n/a

(count:2749 , 50 per page) page: 1 2 3 4 5 6 7 ... 55

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:34524095-34524145	Jurkat	blood:	n/a
2	chr6:34511514-34511564	RPTEC	kidney:	n/a
3	chr6:34489623-34489673	PrEC	prostate:	n/a
4	chr6:34525026-34525076	HL-60	blood:	n/a
5	chr6:34524095-34524145	Jurkat	blood:	n/a
6	chr6:34511514-34511564	RPTEC	kidney:	n/a
7	chr6:34489623-34489673	PrEC	prostate:	n/a
8	chr6:34525026-34525076	HL-60	blood:	n/a
9	chr6:34499314-34499364	SK-N-SH_RA	brain:	n/a
10	chr6:34499504-34499554	AoSMC	blood vessel:	n/a
11	chr6:34486129-34486179	HCF	heart:	n/a
12	chr6:34524766-34524816	ProgFib	skin:	n/a
13	chr6:34494976-34495026	NHDF-neo	bronchial:	n/a
14	chr6:34495124-34495174	HEK293	kidney:	embryo
15	chr6:34524698-34524748	HUVEC	blood vessel:	n/a
16	chr6:34523925-34523975	HRPEpiC	eye:	n/a
17	chr6:34524290-34524340	HCM	heart:	n/a
18	chr6:34482479-34482529	NH-A	brain:	n/a
19	chr6:34505610-34505660	AoSMC	blood vessel:	n/a
20	chr6:34495393-34495443	HEEpiC	esophagus:	n/a
21	chr6:34495054-34495104	AG04449	skin:	fetal
22	chr6:34464251-34464301	Hela-S3	cervix:	n/a
23	chr6:34498714-34498764	GM19239	blood:	n/a
24	chr6:34499488-34499538	NHDF-neo	bronchial:	n/a
25	chr6:34495393-34495443	A549	lung:	n/a
26	chr6:34524278-34524328	Caco-2	colon:	n/a
27	chr6:34458902-34458952	HRE	kidney:	n/a
28	chr6:34495393-34495443	MCF-7	breast:	n/a
29	chr6:34523925-34523975	HCT-116	colon:	n/a
30	chr6:34498714-34498764	U87	brain:	n/a
31	chr6:34512215-34512265	GM06990	blood:	n/a
32	chr6:34524095-34524145	Caco-2	colon:	n/a
33	chr6:34528827-34528877	CMK	blood:	n/a
34	chr6:34482411-34482461	HRCEpiC	kidney:	n/a
35	chr6:34512215-34512265	BJ	skin:	n/a
36	chr6:34489552-34489602	PANC-1	pancreas:	n/a
37	chr6:34495393-34495443	HCM	heart:	n/a
38	chr6:34498714-34498764	HCM	heart:	n/a
39	chr6:34499314-34499364	H1-hESC	embryonic stem cell:	embryo
40	chr6:34499389-34499439	HEK293	kidney:	embryo
41	chr6:34495308-34495358	Caco-2	colon:	n/a
42	chr6:34501193-34501243	HCPEpiC	choroid plexus:	n/a
43	chr6:34499389-34499439	NHBE	bronchial:	n/a
44	chr6:34524698-34524748	PrEC	prostate:	n/a
45	chr6:34543055-34543105	SK-N-MC	brain:	n/a
46	chr6:34512215-34512265	GM12892	blood:	n/a
47	chr6:34489785-34489835	HCT-116	colon:	n/a
48	chr6:34482479-34482529	MCF-7	breast:	n/a
49	chr6:34524290-34524340	NH-A	brain:	n/a
50	chr6:34523925-34523975	Caco-2	colon:	n/a

(count:192 , 50 per page) page: 1 2 3 4

No.	Distal block	Cell Line	Cell type
1	chr6:34511760..34514306-chr6:34515453..34517552,2	K562	blood:
2	chr6:34205000..34207351-chr6:34521778..34524214,3	MCF-7	breast:
3	chr6:34535538..34537048-chr6:34550660..34552218,2	K562	blood:
4	chr6:34495305..34497309-chr6:34500179..34501973,2	K562	blood:
5	chr6:34193853..34195785-chr6:34492922..34495154,2	K562	blood:
6	chr6:34439344..34441190-chr6:34462039..34464180,2	K562	blood:
7	chr6:34494831..34497738-chr6:34508657..34510396,2	MCF-7	breast:
8	chr6:34496972..34497706-chr6:34576720..34577905,3	MCF-7	breast:
9	chr6:34494831..34497738-chr6:34508657..34510396,2	MCF-7	breast:
10	chr6:34482918..34485421-chr6:35035460..35037570,2	K562	blood:
11	chr6:34467900..34469881-chr6:34479800..34481611,2	K562	blood:
12	chr20:52484501..52486317-chr6:34526583..34529198,2	MCF-7	breast:
13	chr6:34494608..34496228-chr6:34576974..34578003,14	K562	blood:
14	chr6:34509583..34511363-chr6:34518250..34520010,2	K562	blood:
15	chr6:34497164..34498159-chr6:34514567..34515376,2	MCF-7	breast:
16	chr6:34478801..34483587-chr6:34487248..34491572,6	K562	blood:
17	chr6:34480102..34483166-chr6:34493351..34495807,3	MCF-7	breast:
18	chr6:34473007..34475169-chr6:34486448..34488656,2	K562	blood:
19	chr6:34481114..34483145-chr6:34525090..34526631,2	K562	blood:
20	chr6:34473007..34475169-chr6:34486448..34488656,2	K562	blood:
21	chr6:34496034..34498791-chr6:34510835..34512433,2	K562	blood:
22	chr6:34493240..34495795-chr6:34548549..34550240,2	K562	blood:
23	chr6:34528981..34530580-chr6:34530582..34532257,2	MCF-7	breast:
24	chr6:34497164..34498159-chr6:34514567..34515376,2	MCF-7	breast:
25	chr6:34525385..34526922-chr6:34526989..34528671,2	K562	blood:
26	chr6:34514095..34516338-chr6:34543578..34545622,2	MCF-7	breast:
27	chr6:34497242..34499881-chr6:34564591..34566557,2	MCF-7	breast:
28	chr6:34508361..34510823-chr6:34510978..34513076,2	MCF-7	breast:
29	chr6:34496034..34498791-chr6:34510835..34512433,2	K562	blood:
30	chr6:34502654..34506400-chr6:34510960..34515406,9	MCF-7	breast:
31	chr6:34509583..34511363-chr6:34518250..34520010,2	K562	blood:
32	chr6:34501160..34503078-chr6:34510332..34511859,2	K562	blood:
33	chr6:34514887..34517520-chr6:34540730..34542846,2	MCF-7	breast:
34	chr6:34490255..34493000-chr6:34512065..34514942,2	K562	blood:
35	chr6:34496932..34498060-chr6:34528153..34529212,4	MCF-7	breast:
36	chr6:34479843..34482340-chr6:34557175..34560153,2	K562	blood:
37	chr6:34502860..34505153-chr6:34574324..34576111,2	MCF-7	breast:
38	chr6:34522438..34524089-chr6:34549801..34552822,3	MCF-7	breast:
39	chr6:34496932..34498060-chr6:34528153..34529212,4	MCF-7	breast:
40	chr6:34471689..34473248-chr6:34481488..34483012,2	K562	blood:
41	chr6:34531920..34532420-chr9:133836898..133837416,2	Hela-S3	cervix:
42	chr6:34514887..34517520-chr6:34540730..34542846,2	MCF-7	breast:
43	chr6:34500365..34503301-chr6:34563391..34565656,2	K562	blood:
44	chr6:34265209..34267014-chr6:34530646..34533613,2	K562	blood:
45	chr6:34430065..34432112-chr6:34462905..34465390,2	MCF-7	breast:
46	chr6:34439690..34441668-chr6:34462680..34464330,2	K562	blood:
47	chr6:34203553..34206354-chr6:34501121..34502681,2	K562	blood:
48	chr6:34527055..34529917-chr6:34543453..34544974,2	MCF-7	breast:
49	chr6:34502047..34504010-chr6:34512836..34514494,2	K562	blood:
50	chr6:34529337..34532289-chr6:34533729..34536883,4	K562	blood:

No data

Variant related genes	Relation type
ENSG00000196114	TF binding region
SPDEF	TF binding region
PACSIN1	TF binding region
ENSG00000196114	CpG island
SPDEF	CpG island
PACSIN1	CpG island
ENSG00000124614	chromatin interactions
ENSG00000221635	chromatin interactions
ENSG00000137309	chromatin interactions
ENSG00000270800	chromatin interactions
ENSG00000204257	chromatin interactions
ENSG00000124507	chromatin interactions
ENSG00000186577	chromatin interactions
ENSG00000196114	chromatin interactions
ENSG00000223837	chromatin interactions
ENSG00000124664	chromatin interactions
ENSG00000204256	chromatin interactions

Extended variants
information (count: 3711 )
Associated
traits (count: 107 )

Variant overlapped rSNPs/rCNVs (count:3711 , 50 per page) page: 1 2 3 4 5 6 7 ... 75

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs547435646	chr6:34455255-34455256	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs374265360	chr6:34455269-34455270	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs559693808	chr6:34455284-34455285	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs142661973	chr6:34455297-34455298	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs7748484	chr6:34455330-34455331	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs7748495	chr6:34455348-34455349	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs184142770	chr6:34455387-34455388	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs189867696	chr6:34455392-34455393	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs76439083	chr6:34455443-34455444	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs9380440	chr6:34455449-34455450	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs77767536	chr6:34455473-34455474	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs143383157	chr6:34455483-34455484	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs535480837	chr6:34455496-34455497	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs78380702	chr6:34455509-34455510	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs575632691	chr6:34455513-34455514	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs545634772	chr6:34455592-34455593	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs560807019	chr6:34455616-34455617	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs376241665	chr6:34455643-34455644	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs145914055	chr6:34455650-34455651	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs529287064	chr6:34455708-34455709	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs373991017	chr6:34455734-34455735	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs534604348	chr6:34455738-34455739	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs148356818	chr6:34455749-34455750	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs559625105	chr6:34455788-34455789	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs191877794	chr6:34455798-34455799	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs141503909	chr6:34455809-34455810	Weak transcription Enhancers Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs376065816	chr6:34455837-34455838	Weak transcription Enhancers Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs150117187	chr6:34455850-34455851	Weak transcription Enhancers Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs531117226	chr6:34455884-34455885	Weak transcription Enhancers Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs112280338	chr6:34455893-34455894	Weak transcription Enhancers Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs370407269	chr6:34455918-34455919	Weak transcription Enhancers Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs60214378	chr6:34455930-34455931	Weak transcription Enhancers Bivalent/Poised TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs141634736	chr6:34456046-34456047	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
34	rs183963496	chr6:34456087-34456088	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
35	rs189081256	chr6:34456100-34456101	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
36	rs568180183	chr6:34456121-34456122	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
37	rs535413497	chr6:34456123-34456124	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
38	rs556999670	chr6:34456165-34456166	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
39	rs569133392	chr6:34456181-34456182	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
40	rs539712410	chr6:34456206-34456207	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
41	rs547935100	chr6:34456253-34456254	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
42	rs146195780	chr6:34456358-34456359	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
43	rs572976752	chr6:34456393-34456394	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
44	rs139074981	chr6:34456431-34456432	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs568137090	chr6:34456438-34456439	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs553021168	chr6:34456456-34456457	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs181456643	chr6:34456526-34456527	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs541777724	chr6:34456539-34456540	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs187505195	chr6:34456567-34456568	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs530859231	chr6:34456617-34456618	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:107)

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
Acute myeloid leukemia	20729466	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
Esophageal adenocarcinoma	18820669	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
Oral squamous cell carcinoma	17134496	CNVD
Gastric cancer	17908304	CNVD
Metanephric adenoma	20802469	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Schizophrenia	19571808	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Neuroblastoma	16790693	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Breast cancer	16397240	CNVD
Retinoblastoma	22278416	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Systemic lupus erythematosus	20877625	CNVD
Cleidocranial dysplasia	18696259	CNVD
Holoprosencephaly	21359414	CNVD
Liposarcoma	21253554	CNVD
Uveal melanoma	20484589	CNVD
Fibroblasts	20926602	CNVD
Systemic lupus erythematosus	19279649	CNVD
Retinoblastoma	16790693	CNVD
Acute myocardial infarction	18032375	CNVD
Renal cell carcinoma	19150565	CNVD
Systemic lupus erythematosus	19591781	CNVD
Attention deficit hyperactivity disorder	19287146	CNVD
Autism	19287146	CNVD
Erythema nodosum in leprosy	19287146	CNVD
Henoch-schoenlein purpura	19287146	CNVD
Liver cirrhosis	19287146	CNVD
Systemic lupus erythematosus	19287146	CNVD
Autoimmune disease	19135723	CNVD
Congenital adrenal hyperplasia	18478071	CNVD
Systemic lupus erythematosus	19287147	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
Cancer	22183965	CNVD
Melanoma	22183965	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Lung cancer	18438408	CNVD
Glioblastoma multiforme	21138945	CNVD
Breast cancer	21364760	CNVD
Basal cell lymphoma	19029149	CNVD
Diffuse large b-cell lymphoma	19029149	CNVD
Myelofibrosis	22110671	CNVD
Liver carcinoma	19366792	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Amyotrophic lateral sclerosis	20685689	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:1575 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:34441400-34494000	Weak transcription	Right Atrium	heart
2	chr6:34444600-34468200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
3	chr6:34451000-34458800	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
4	chr6:34453200-34458400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
5	chr6:34453200-34458400	Weak transcription	HUES6 Cell Line	embryonic stem cell
6	chr6:34453400-34458200	Weak transcription	K562	blood
7	chr6:34454400-34455400	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
8	chr6:34454400-34455800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
9	chr6:34454400-34456000	Weak transcription	Primary hematopoietic stem cells	blood
10	chr6:34454400-34458200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
11	chr6:34454400-34458400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
12	chr6:34454400-34459000	Weak transcription	NHEK	skin
13	chr6:34454400-34461000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
14	chr6:34454400-34464800	Weak transcription	Thymus	Thymus
15	chr6:34454600-34455600	Weak transcription	Primary T helper cells PMA-I stimulated	--
16	chr6:34454600-34455800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
17	chr6:34455000-34455800	Weak transcription	Primary T cells fromperipheralblood	blood
18	chr6:34455000-34458400	Weak transcription	Fetal Thymus	thymus
19	chr6:34455200-34459800	Enhancers	Primary hematopoietic stem cells short term culture	blood
20	chr6:34455400-34456200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
21	chr6:34455600-34455800	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
22	chr6:34455600-34455800	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
23	chr6:34455800-34456000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
24	chr6:34455800-34456000	Enhancers	Primary T cells fromperipheralblood	blood
25	chr6:34455800-34456000	Enhancers	Primary T helper cells PMA-I stimulated	--
26	chr6:34455800-34456000	Bivalent/Poised TSS	Foreskin Fibroblast Primary Cells skin02	Skin
27	chr6:34455800-34456400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
28	chr6:34455800-34456400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
29	chr6:34456000-34456200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
30	chr6:34456000-34456400	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
31	chr6:34456000-34456600	Enhancers	Primary hematopoietic stem cells	blood
32	chr6:34456000-34457200	Weak transcription	Primary T cells fromperipheralblood	blood
33	chr6:34456000-34458800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
34	chr6:34456200-34458400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
35	chr6:34456200-34459200	Weak transcription	Right Ventricle	heart
36	chr6:34456400-34458200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
37	chr6:34456400-34458800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
38	chr6:34456600-34458400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
39	chr6:34456600-34458400	Weak transcription	Primary hematopoietic stem cells	blood
40	chr6:34457200-34457400	Enhancers	Primary T cells fromperipheralblood	blood
41	chr6:34457400-34458600	Weak transcription	H1 Cell Line	embryonic stem cell
42	chr6:34457800-34458200	Enhancers	Skeletal Muscle Male	skeletal muscle
43	chr6:34458000-34458400	Enhancers	HSMM	muscle
44	chr6:34458000-34459400	Enhancers	Fetal Muscle Leg	muscle
45	chr6:34458000-34459600	Enhancers	Fetal Stomach	stomach
46	chr6:34458200-34458400	Enhancers	Muscle Satellite Cultured Cells	--
47	chr6:34458200-34458400	Enhancers	Skeletal Muscle Female	skeletal muscle
48	chr6:34458200-34458600	Enhancers	Ovary	ovary
49	chr6:34458200-34459000	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
50	chr6:34458200-34459000	Enhancers	K562	blood

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