Variant report

Variant	nsv885789
Chromosome Location	chr6:34474939-34546560
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1919)
CpG islands
(count:2628)
Chromatin interactive
region (count:175)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1919 , 50 per page) page: 1 2 3 4 5 6 7 ... 39

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:34485472-34485719	K562	blood:	n/a	n/a
2	ARID3A	chr6:34537168-34537342	K562	blood:	n/a	n/a
3	ARID3A	chr6:34528420-34528567	HepG2	liver:	n/a	n/a
4	ARID3A	chr6:34528321-34529035	K562	blood:	n/a	n/a
5	ARID3A	chr6:34530717-34531006	K562	blood:	n/a	n/a
6	ARID3A	chr6:34494959-34495288	HepG2	liver:	n/a	n/a
7	ARID3A	chr6:34494652-34494762	K562	blood:	n/a	n/a
8	ARID3A	chr6:34495041-34495171	K562	blood:	n/a	n/a
9	ARID3A	chr6:34535143-34535361	HepG2	liver:	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	chr6:34485205-34485489	K562	blood:	n/a	n/a
15	BACH1	chr6:34525098-34525122	K562	blood:	n/a	n/a
16	BACH1	chr6:34494673-34494811	K562	blood:	n/a	n/a
17	BACH1	chr6:34528081-34528565	K562	blood:	n/a	n/a
18	BCL3	chr6:34522693-34523062	GM12878	blood:	n/a	n/a
19	BCL3	chr6:34522720-34523036	GM12878	blood:	n/a	n/a
20	BCL3	chr6:34541372-34541610	GM12878	blood:	n/a	n/a
21	BCL3	chr6:34543140-34543668	K562	blood:	n/a	chr6:34543350-34543359
22	BCLAF1	chr6:34494974-34495328	GM12878	blood:	n/a	n/a
23	BHLHE40	chr6:34495040-34495240	GM12878	blood:	n/a	n/a
24	BHLHE40	chr6:34535821-34536274	HepG2	liver:	n/a	n/a
25	BHLHE40	chr6:34526077-34526348	K562	blood:	n/a	n/a
26	BHLHE40	chr6:34481627-34482576	K562	blood:	n/a	n/a
27	BHLHE40	chr6:34527683-34529135	K562	blood:	n/a	n/a
28	BHLHE40	chr6:34531305-34531454	K562	blood:	n/a	n/a
29	BHLHE40	chr6:34498559-34498914	K562	blood:	n/a	n/a
30	BHLHE40	chr6:34525097-34525230	K562	blood:	n/a	n/a
31	BHLHE40	chr6:34535812-34536294	K562	blood:	n/a	n/a
32	BHLHE40	chr6:34528358-34529016	HepG2	liver:	n/a	n/a
33	BHLHE40	chr6:34512632-34512964	K562	blood:	n/a	n/a
34	BHLHE40	chr6:34494998-34495331	K562	blood:	n/a	n/a
35	BHLHE40	chr6:34530292-34531071	K562	blood:	n/a	n/a
36	BRCA1	chr6:34495142-34495167	HepG2	liver:	n/a	n/a
37	BRCA1	chr6:34528383-34528433	HepG2	liver:	n/a	n/a
38	BRCA1	chr6:34528656-34528787	HepG2	liver:	n/a	n/a
39	BRCA1	chr6:34534813-34534889	H1-hESC	embryonic stem cell:	n/a	n/a
40	BRCA1	chr6:34539475-34539630	HepG2	liver:	n/a	n/a
41	BRCA1	chr6:34495129-34495249	GM12878	blood:	n/a	n/a
42	CBX3	chr6:34540358-34540680	K562	blood:	n/a	n/a
43	CBX3	chr6:34504717-34505022	K562	blood:	n/a	n/a
44	CBX3	chr6:34512311-34513045	K562	blood:	n/a	n/a
45	CBX3	chr6:34530537-34531593	K562	blood:	n/a	n/a
46	CBX3	chr6:34499300-34499739	K562	blood:	n/a	n/a
47	CBX3	chr6:34536960-34537774	K562	blood:	n/a	n/a
48	CBX3	chr6:34529829-34530430	K562	blood:	n/a	n/a
49	CBX3	chr6:34525886-34526725	K562	blood:	n/a	n/a
50	CBX3	chr6:34528147-34529296	K562	blood:	n/a	n/a

(count:2628 , 50 per page) page: 1 2 3 4 5 6 7 ... 53

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:34523925-34523975	HNPCEpiC	eye:	n/a
2	chr6:34492115-34492165	NHBE	bronchial:	n/a
3	chr6:34524095-34524145	AG10803	skin:	n/a
4	chr6:34511514-34511564	HRE	kidney:	n/a
5	chr6:34535602-34535652	PANC-1	pancreas:	n/a
6	chr6:34523925-34523975	HNPCEpiC	eye:	n/a
7	chr6:34492115-34492165	NHBE	bronchial:	n/a
8	chr6:34524095-34524145	AG10803	skin:	n/a
9	chr6:34511514-34511564	HRE	kidney:	n/a
10	chr6:34535602-34535652	PANC-1	pancreas:	n/a
11	chr6:34502119-34502169	U87	brain:	n/a
12	chr6:34495124-34495174	U87	brain:	n/a
13	chr6:34494976-34495026	GM12878	blood:	n/a
14	chr6:34524290-34524340	HCPEpiC	choroid plexus:	n/a
15	chr6:34514887-34514937	HCT-116	colon:	n/a
16	chr6:34495292-34495342	K562	blood:	n/a
17	chr6:34495124-34495174	NHBE	bronchial:	n/a
18	chr6:34524597-34524647	PrEC	prostate:	n/a
19	chr6:34524097-34524147	HL-60	blood:	n/a
20	chr6:34511514-34511564	HL-60	blood:	n/a
21	chr6:34514887-34514937	NT2-D1	testis:	n/a
22	chr6:34489623-34489673	HRPEpiC	eye:	n/a
23	chr6:34482479-34482529	NHBE	bronchial:	n/a
24	chr6:34494976-34495026	NB4	blood:	n/a
25	chr6:34504890-34504940	HIPEpiC	eye:	n/a
26	chr6:34495308-34495358	H1-hESC	embryonic stem cell:	embryo
27	chr6:34489552-34489602	SK-N-SH_RA	brain:	n/a
28	chr6:34525026-34525076	HRPEpiC	eye:	n/a
29	chr6:34511514-34511564	IMR90	lung:	fetal
30	chr6:34508820-34508870	NB4	blood:	n/a
31	chr6:34524698-34524748	HEK293	kidney:	embryo
32	chr6:34524097-34524147	MCF-7	breast:	n/a
33	chr6:34494976-34495026	MCF10A-Er-Src	breast:	n/a
34	chr6:34499488-34499538	HEK293	kidney:	embryo
35	chr6:34495292-34495342	HCT-116	colon:	n/a
36	chr6:34492115-34492165	IMR90	lung:	fetal
37	chr6:34511514-34511564	U87	brain:	n/a
38	chr6:34495054-34495104	Jurkat	blood:	n/a
39	chr6:34525026-34525076	BE2_C	brain:	n/a
40	chr6:34495292-34495342	HRCEpiC	kidney:	n/a
41	chr6:34498714-34498764	GM12892	blood:	n/a
42	chr6:34524597-34524647	PFSK-1	brain:	n/a
43	chr6:34528827-34528877	Hela-S3	cervix:	n/a
44	chr6:34523925-34523975	SK-N-MC	brain:	n/a
45	chr6:34495393-34495443	SK-N-SH	brain:	n/a
46	chr6:34524698-34524748	H1-hESC	embryonic stem cell:	embryo
47	chr6:34524290-34524340	HEK293	kidney:	embryo
48	chr6:34504890-34504940	RPTEC	kidney:	n/a
49	chr6:34495308-34495358	AoSMC	blood vessel:	n/a
50	chr6:34524766-34524816	K562	blood:	n/a

(count:175 , 50 per page) page: 1 2 3 4

No.	Distal block	Cell Line	Cell type
1	chr6:34528981..34530580-chr6:34530582..34532257,2	MCF-7	breast:
2	chr6:34527129..34529225-chr6:34531595..34533511,2	K562	blood:
3	chr6:34502654..34506400-chr6:34510960..34515406,9	MCF-7	breast:
4	chr18:50300436..50303454-chr6:34521553..34523812,3	MCF-7	breast:
5	chr6:34509583..34511363-chr6:34518250..34520010,2	K562	blood:
6	chr6:34497164..34498159-chr6:34514567..34515376,2	MCF-7	breast:
7	chr6:34494680..34495634-chr6:34577124..34578035,2	MCF-7	breast:
8	chr6:34392344..34394131-chr6:34485515..34488152,2	MCF-7	breast:
9	chr6:34527055..34529917-chr6:34543453..34544974,2	MCF-7	breast:
10	chr6:34498077..34501386-chr6:34521162..34524580,5	MCF-7	breast:
11	chr6:34494873..34497912-chr6:34521168..34524393,3	MCF-7	breast:
12	chr6:34522370..34525112-chr6:34541822..34544372,2	MCF-7	breast:
13	chr6:34467900..34469881-chr6:34479800..34481611,2	K562	blood:
14	chr6:34503128..34505845-chr6:34536309..34539232,2	K562	blood:
15	chr6:33686485..33689308-chr6:34514444..34516167,2	MCF-7	breast:
16	chr6:34508361..34510823-chr6:34510978..34513076,2	MCF-7	breast:
17	chr6:34435937..34438924-chr6:34520705..34523320,2	MCF-7	breast:
18	chr6:34193853..34195785-chr6:34492922..34495154,2	K562	blood:
19	chr6:34508152..34511012-chr6:34535080..34537020,2	K562	blood:
20	chr6:34497164..34498159-chr6:34514567..34515376,2	MCF-7	breast:
21	chr6:34514736..34516500-chr6:34519380..34521095,2	K562	blood:
22	chr6:34216948..34217455-chr6:34494244..34495154,2	K562	blood:
23	chr6:34392122..34394769-chr6:34484258..34486881,2	K562	blood:
24	chr6:34392363..34395361-chr6:34495918..34498856,2	K562	blood:
25	chr6:34502654..34506400-chr6:34510960..34515406,9	MCF-7	breast:
26	chr6:34481304..34483971-chr6:34501598..34503855,2	K562	blood:
27	chr6:34494545..34497462-chr6:34498275..34503019,6	MCF-7	breast:
28	chr6:34536153..34538160-chr6:34545936..34548526,2	MCF-7	breast:
29	chr6:34527602..34533050-chr6:34533572..34539589,8	K562	blood:
30	chr6:34511760..34514306-chr6:34515453..34517552,2	K562	blood:
31	chr6:34506980..34511719-chr6:34518115..34520438,4	K562	blood:
32	chr6:34189603..34191937-chr6:34485538..34487216,2	MCF-7	breast:
33	chr6:34475212..34479816-chr6:34480006..34482829,5	K562	blood:
34	chr6:34480102..34483166-chr6:34493351..34495807,3	MCF-7	breast:
35	chr6:34527129..34530623-chr6:34530939..34533511,3	K562	blood:
36	chr6:34508607..34511346-chr6:34567639..34570139,2	K562	blood:
37	chr6:34528906..34533005-chr6:34533870..34536568,4	MCF-7	breast:
38	chr6:34265209..34267014-chr6:34530646..34533613,2	K562	blood:
39	chr6:34473007..34475169-chr6:34486448..34488656,2	K562	blood:
40	chr6:34504144..34505003-chr6:34514225..34514901,2	MCF-7	breast:
41	chr6:34521648..34524118-chr6:34538318..34540666,2	MCF-7	breast:
42	chr6:34514887..34517520-chr6:34540730..34542846,2	MCF-7	breast:
43	chr6:34483206..34485571-chr6:34540552..34542756,2	K562	blood:
44	chr6:34503128..34505845-chr6:34536309..34539232,2	K562	blood:
45	chr6:34391920..34394016-chr6:34508628..34510815,2	MCF-7	breast:
46	chr6:34525385..34526922-chr6:34526989..34528671,2	K562	blood:
47	chr6:34501160..34503078-chr6:34510332..34511859,2	K562	blood:
48	chr6:34500365..34503301-chr6:34563391..34565656,2	K562	blood:
49	chr6:34528981..34530580-chr6:34530582..34532257,2	MCF-7	breast:
50	chr6:34490944..34493717-chr6:34499736..34502529,2	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
ENSG00000124507	chromatin interactions
ENSG00000186577	chromatin interactions
ENSG00000270800	chromatin interactions
ENSG00000221635	chromatin interactions
ENSG00000137309	chromatin interactions
ENSG00000223837	chromatin interactions
ENSG00000204257	chromatin interactions
ENSG00000124664	chromatin interactions
ENSG00000124614	chromatin interactions
ENSG00000196114	chromatin interactions
ENSG00000204256	chromatin interactions

Extended variants
information (count: 3048 )
Associated
traits (count: 107 )

Variant overlapped rSNPs/rCNVs (count:3048 , 50 per page) page: 1 2 3 4 5 6 7 ... 61

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4713807	chr6:34474939-34474940	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs189066399	chr6:34474986-34474987	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs577067224	chr6:34474997-34474998	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs534836497	chr6:34475048-34475049	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs554205141	chr6:34475082-34475083	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs572432998	chr6:34475100-34475101	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs181462848	chr6:34475114-34475115	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs4711394	chr6:34475118-34475119	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs114695975	chr6:34475119-34475120	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs186353578	chr6:34475139-34475140	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs565239601	chr6:34475168-34475169	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs144535939	chr6:34475185-34475186	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs547686895	chr6:34475187-34475188	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs190474579	chr6:34475194-34475195	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs73407704	chr6:34475224-34475225	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs565889042	chr6:34475295-34475296	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs548308668	chr6:34475323-34475324	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs374878133	chr6:34475328-34475329	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs57453362	chr6:34475334-34475335	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs56658381	chr6:34475339-34475340	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs397959229	chr6:34475340-34475341	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs552473863	chr6:34475359-34475360	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs528705813	chr6:34475442-34475443	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs553657552	chr6:34475443-34475444	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs570775834	chr6:34475454-34475455	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs190747806	chr6:34475465-34475466	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs151212004	chr6:34475510-34475511	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs574622588	chr6:34475556-34475557	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs60793757	chr6:34475576-34475577	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs182805223	chr6:34475606-34475607	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs562646000	chr6:34475612-34475613	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs575980477	chr6:34475740-34475741	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs140301561	chr6:34475770-34475771	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs185624129	chr6:34475778-34475779	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs577103080	chr6:34475796-34475797	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs541735300	chr6:34475797-34475798	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs12197759	chr6:34475822-34475823	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs530328233	chr6:34475833-34475834	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs547931175	chr6:34475842-34475843	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs201359226	chr6:34475875-34475876	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs145011394	chr6:34475877-34475878	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs376206893	chr6:34475878-34475879	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs572198482	chr6:34475882-34475883	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs373870498	chr6:34475883-34475884	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs374870464	chr6:34475897-34475898	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs530485734	chr6:34475902-34475903	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs150362769	chr6:34475911-34475912	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs570489802	chr6:34475914-34475915	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs190734885	chr6:34475916-34475917	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs546913918	chr6:34475961-34475962	Weak transcription	Chromatin interactive region	1 gene(s)	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
Non-syndromic sensorineural hearing loss	17122850	CNVD
Amyotrophic lateral sclerosis	20685689	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:1471 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:34441400-34494000	Weak transcription	Right Atrium	heart
2	chr6:34474000-34475200	Enhancers	ES-WA7 Cell Line	embryonic stem cell
3	chr6:34474400-34475000	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
4	chr6:34474400-34475200	Enhancers	iPS-15b Cell Line	embryonic stem cell
5	chr6:34474400-34475200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
6	chr6:34474400-34475200	Enhancers	HSMMtube	muscle
7	chr6:34474600-34475000	Enhancers	ES-I3 Cell Line	embryonic stem cell
8	chr6:34474600-34475200	Enhancers	iPS-18 Cell Line	embryonic stem cell
9	chr6:34474600-34475600	Enhancers	K562	blood
10	chr6:34474800-34475200	Enhancers	HUES64 Cell Line	embryonic stem cell
11	chr6:34474800-34479600	Weak transcription	H1 Cell Line	embryonic stem cell
12	chr6:34474800-34481400	Weak transcription	HUES6 Cell Line	embryonic stem cell
13	chr6:34474800-34481600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
14	chr6:34475000-34475400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
15	chr6:34475000-34479800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
16	chr6:34475200-34475400	Weak transcription	HSMMtube	muscle
17	chr6:34475200-34479600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
18	chr6:34475200-34480400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
19	chr6:34475200-34480600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
20	chr6:34475200-34480800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
21	chr6:34475400-34475600	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
22	chr6:34475600-34480400	Weak transcription	K562	blood
23	chr6:34475600-34480800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
24	chr6:34479000-34479600	Enhancers	Brain Germinal Matrix	brain
25	chr6:34479000-34480600	Enhancers	Cortex derived primary cultured neurospheres	brain
26	chr6:34479000-34480600	Enhancers	Brain Inferior Temporal Lobe	brain
27	chr6:34479000-34485200	Enhancers	Fetal Brain Male	brain
28	chr6:34479400-34480400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
29	chr6:34479600-34479800	Enhancers	ES-WA7 Cell Line	embryonic stem cell
30	chr6:34479600-34479800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
31	chr6:34479600-34479800	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
32	chr6:34479600-34479800	Enhancers	Brain Anterior Caudate	brain
33	chr6:34479600-34480000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
34	chr6:34479600-34480000	Flanking Active TSS	Brain Germinal Matrix	brain
35	chr6:34479600-34480200	Enhancers	Fetal Brain Female	brain
36	chr6:34479600-34482000	Enhancers	H1 Cell Line	embryonic stem cell
37	chr6:34479600-34482000	Enhancers	Brain Angular Gyrus	brain
38	chr6:34479600-34482400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
39	chr6:34479800-34480400	Enhancers	Fetal Muscle Trunk	muscle
40	chr6:34479800-34480600	Enhancers	ES-I3 Cell Line	embryonic stem cell
41	chr6:34479800-34480600	Weak transcription	Brain Anterior Caudate	brain
42	chr6:34479800-34481200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
43	chr6:34479800-34481800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
44	chr6:34480000-34482200	Enhancers	Brain Germinal Matrix	brain
45	chr6:34480200-34480400	Weak transcription	HUES64 Cell Line	embryonic stem cell
46	chr6:34480200-34480600	Weak transcription	Fetal Brain Female	brain
47	chr6:34480400-34480600	Enhancers	HUES64 Cell Line	embryonic stem cell
48	chr6:34480400-34480600	Enhancers	iPS-15b Cell Line	embryonic stem cell
49	chr6:34480400-34482200	Enhancers	HUES48 Cell Line	embryonic stem cell
50	chr6:34480400-34482200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain

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