Variant report

Variant	nsv965712
Chromosome Location	chr6:34177749-34192058
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:447)
CpG islands
(count:183)
Chromatin interactive
region (count:35)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:447 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr6:34191736-34192248	GM12878	blood:	n/a	n/a
2	ATF3	chr6:34191773-34192208	K562	blood:	n/a	chr6:34192082-34192096
3	ATF3	chr6:34191620-34192294	K562	blood:	n/a	chr6:34192082-34192096
4	BACH1	chr6:34191918-34192050	K562	blood:	n/a	chr6:34191918-34191932
5	BACH1	chr6:34191713-34192462	H1-hESC	embryonic stem cell:	n/a	chr6:34191918-34191932
6	BATF	chr6:34191828-34192143	GM12878	blood:	n/a	n/a
7	BCL11A	chr6:34191856-34192174	GM12878	blood:	n/a	chr6:34191929-34191938 chr6:34192112-34192125
8	BCL11A	chr6:34191827-34192175	GM12878	blood:	n/a	chr6:34191929-34191938 chr6:34192112-34192125
9	BCL3	chr6:34191695-34192206	A549	lung:	n/a	chr6:34191785-34191794 chr6:34191929-34191938 chr6:34192112-34192125
10	BCL3	chr6:34191706-34192266	GM12878	blood:	n/a	chr6:34191785-34191794 chr6:34191929-34191938 chr6:34192112-34192125
11	BCLAF1	chr6:34191814-34192221	GM12878	blood:	n/a	chr6:34191929-34191938 chr6:34192112-34192125
12	BCLAF1	chr6:34191735-34192304	GM12878	blood:	n/a	chr6:34191785-34191794 chr6:34191929-34191938 chr6:34192112-34192125
13	BHLHE40	chr6:34191677-34192202	HepG2	liver:	n/a	n/a
14	BHLHE40	chr6:34191720-34192605	GM12878	blood:	n/a	n/a
15	BHLHE40	chr6:34191605-34192553	K562	blood:	n/a	n/a
16	BRCA1	chr6:34191809-34192025	Hela-S3	cervix:	n/a	n/a
17	CBX3	chr6:34191140-34192412	K562	blood:	n/a	n/a
18	CCNT2	chr6:34191655-34192284	K562	blood:	n/a	n/a
19	CEBPB	chr6:34182851-34183040	K562	blood:	n/a	n/a
20	CEBPB	chr6:34191749-34192129	Hela-S3	cervix:	n/a	n/a
21	CEBPB	chr6:34182867-34183143	K562	blood:	n/a	n/a
22	CEBPB	chr6:34192038-34192090	HepG2	liver:	n/a	n/a
23	CHD1	chr6:34191980-34192401	GM12878	blood:	n/a	n/a
24	CHD2	chr6:34191980-34192399	HepG2	liver:	n/a	n/a
25	CHD2	chr6:34191657-34192194	Hela-S3	cervix:	n/a	n/a
26	CHD2	chr6:34191193-34192070	H1-hESC	embryonic stem cell:	n/a	chr6:34191477-34191487 chr6:34191282-34191292
27	CHD2	chr6:34191570-34192406	GM12878	blood:	n/a	n/a
28	CHD2	chr6:34191847-34192357	K562	blood:	n/a	n/a
29	CREB1	chr6:34191739-34192080	A549	lung:	n/a	n/a
30	CREB1	chr6:34191654-34192310	GM12878	blood:	n/a	n/a
31	CREB1	chr6:34191388-34192407	HepG2	liver:	n/a	chr6:34192314-34192327
32	CTCF	chr6:34191896-34191927	Pancreas_OC	pancreas:	n/a	n/a
33	CTCF	chr6:34191951-34191960	Spleen_OC	spleen:	n/a	n/a
34	CTCF	chr6:34191707-34191740	Lung_OC	lung:	n/a	n/a
35	CTCF	chr6:34191897-34191950	Spleen_OC	spleen:	n/a	n/a
36	CUX1	chr6:34191964-34192488	K562	blood:	n/a	n/a
37	E2F4	chr6:34191701-34192015	MCF10A-Er-Src	breast:	n/a	n/a
38	E2F4	chr6:34191316-34192421	K562	blood:	n/a	n/a
39	E2F6	chr6:34191746-34191974	K562	blood:	n/a	n/a
40	E2F6	chr6:34191359-34191631	K562	blood:	n/a	n/a
41	E2F6	chr6:34191986-34192195	K562	blood:	n/a	n/a
42	E2F6	chr6:34191335-34192467	K562	blood:	n/a	n/a
43	E2F6	chr6:34191705-34192448	K562	blood:	n/a	n/a
44	EBF1	chr6:34191587-34192240	GM12878	blood:	n/a	n/a
45	EBF1	chr6:34191646-34192099	GM12878	blood:	n/a	n/a
46	EBF1	chr6:34191619-34192258	GM12878	blood:	n/a	n/a
47	EGR1	chr6:34191797-34192198	GM12878	blood:	n/a	chr6:34192056-34192067 chr6:34192050-34192060 chr6:34192056-34192065 chr6:34192045-34192060 chr6:34192055-34192068 chr6:34192054-34192069 chr6:34192054-34192068
48	EGR1	chr6:34191754-34192265	ECC-1	luminal epithelium:	n/a	chr6:34192056-34192067 chr6:34192050-34192060 chr6:34192056-34192065 chr6:34192045-34192060 chr6:34192055-34192068 chr6:34192054-34192069 chr6:34192054-34192068
49	EGR1	chr6:34191817-34192286	ECC-1	luminal epithelium:	n/a	chr6:34192056-34192067 chr6:34192050-34192060 chr6:34192056-34192065 chr6:34192045-34192060 chr6:34192055-34192068 chr6:34192054-34192069 chr6:34192054-34192068
50	EGR1	chr6:34191674-34192200	GM12878	blood:	n/a	chr6:34192056-34192067 chr6:34192050-34192060 chr6:34192056-34192065 chr6:34192045-34192060 chr6:34192055-34192068 chr6:34192054-34192069 chr6:34192054-34192068

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:34191979-34192029	BE2_C	brain:	n/a
2	chr6:34191048-34191098	HCT-116	colon:	n/a
3	chr6:34191979-34192029	GM06990	blood:	n/a
4	chr6:34191048-34191098	IMR90	lung:	fetal
5	chr6:34192005-34192055	GM06990	blood:	n/a
6	chr6:34192005-34192055	GM19239	blood:	n/a
7	chr6:34191979-34192029	AG04449	skin:	fetal
8	chr6:34191048-34191098	CMK	blood:	n/a
9	chr6:34191979-34192029	AG10803	skin:	n/a
10	chr6:34192005-34192055	HCPEpiC	choroid plexus:	n/a
11	chr6:34191979-34192029	ProgFib	skin:	n/a
12	chr6:34191979-34192029	NB4	blood:	n/a
13	chr6:34191979-34192029	NT2-D1	testis:	n/a
14	chr6:34191048-34191098	GM12878	blood:	n/a
15	chr6:34191048-34191098	HRCEpiC	kidney:	n/a
16	chr6:34191048-34191098	NHBE	bronchial:	n/a
17	chr6:34191048-34191098	GM12891	blood:	n/a
18	chr6:34192005-34192055	Caco-2	colon:	n/a
19	chr6:34191979-34192029	SKMC	muscle:	n/a
20	chr6:34191048-34191098	ProgFib	skin:	n/a
21	chr6:34192005-34192055	MCF-7	breast:	n/a
22	chr6:34191979-34192029	LNCaP	prostate:	n/a
23	chr6:34191048-34191098	HNPCEpiC	eye:	n/a
24	chr6:34192005-34192055	NH-A	brain:	n/a
25	chr6:34191979-34192029	PANC-1	pancreas:	n/a
26	chr6:34191979-34192029	HRPEpiC	eye:	n/a
27	chr6:34191979-34192029	NHBE	bronchial:	n/a
28	chr6:34191048-34191098	T-47D	breast:	n/a
29	chr6:34192005-34192055	AoSMC	blood vessel:	n/a
30	chr6:34192005-34192055	HEK293	kidney:	embryo
31	chr6:34191048-34191098	ovcar-3	ovarian:	n/a
32	chr6:34191979-34192029	PFSK-1	brain:	n/a
33	chr6:34192005-34192055	Hela-S3	cervix:	n/a
34	chr6:34191979-34192029	BJ	skin:	n/a
35	chr6:34191979-34192029	ovcar-3	ovarian:	n/a
36	chr6:34191048-34191098	AG04450	lung:	fetal
37	chr6:34191048-34191098	NB4	blood:	n/a
38	chr6:34191048-34191098	SK-N-SH_RA	brain:	n/a
39	chr6:34192005-34192055	Hepatocyte	liver:	n/a
40	chr6:34191048-34191098	HPAEpiC	pulmonary alveolar:	n/a
41	chr6:34191048-34191098	GM19239	blood:	n/a
42	chr6:34191979-34192029	GM12892	blood:	n/a
43	chr6:34192005-34192055	ovcar-3	ovarian:	n/a
44	chr6:34191979-34192029	HL-60	blood:	n/a
45	chr6:34191979-34192029	K562	blood:	n/a
46	chr6:34192005-34192055	HRE	kidney:	n/a
47	chr6:34192005-34192055	SK-N-SH_RA	brain:	n/a
48	chr6:34191048-34191098	Caco-2	colon:	n/a
49	chr6:34192005-34192055	HRPEpiC	eye:	n/a
50	chr6:34191979-34192029	NHDF-neo	bronchial:	n/a

(count:35 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:34191465..34193341-chr6:34208084..34210074,2	MCF-7	breast:
2	chr6:34161256..34167016-chr6:34189422..34193988,6	K562	blood:
3	chr6:34173602..34176530-chr6:34190625..34192254,2	MCF-7	breast:
4	chr6:34190995..34193306-chr6:34193856..34195513,2	MCF-7	breast:
5	chr6:34172543..34174818-chr6:34176549..34178504,2	K562	blood:
6	chr6:34190218..34193662-chr6:34359296..34361712,5	MCF-7	breast:
7	chr6:34191402..34195529-chr6:34392087..34394261,4	MCF-7	breast:
8	chr6:34191835..34193562-chr6:34195845..34198625,2	MCF-7	breast:
9	chr6:34179251..34181367-chr6:34182622..34184716,2	K562	blood:
10	chr6:34179251..34181367-chr6:34182622..34184716,2	K562	blood:
11	chr6:34162948..34164566-chr6:34191693..34193324,2	MCF-7	breast:
12	chr6:34105117..34107025-chr6:34191466..34193901,2	K562	blood:
13	chr6:34167669..34170205-chr6:34175412..34177855,2	K562	blood:
14	chr6:34173652..34175726-chr6:34179204..34181498,2	MCF-7	breast:
15	chr6:34167374..34170140-chr6:34179886..34181492,2	K562	blood:
16	chr1:11967977..11968756-chr6:34191455..34192420,2	Hela-S3	cervix:
17	chr6:34191468..34193881-chr6:34392359..34395019,3	MCF-7	breast:
18	chr6:34176766..34178294-chr6:34387966..34390024,2	K562	blood:
19	chr6:34182735..34185425-chr6:34186291..34188532,2	K562	blood:
20	chr6:34190283..34196950-chr6:34202449..34206308,21	MCF-7	breast:
21	chr6:34184902..34188225-chr6:34189855..34191947,3	MCF-7	breast:
22	chr6:34127390..34129450-chr6:34190311..34192689,2	MCF-7	breast:
23	chr6:34190763..34192270-chr6:34389997..34392195,2	K562	blood:
24	chr2:174786139..174786641-chr6:34191900..34192438,2	NB4	blood:
25	chr6:34170593..34173037-chr6:34191454..34193047,2	MCF-7	breast:
26	chr6:34163985..34165499-chr6:34190823..34193399,2	MCF-7	breast:
27	chr6:34190794..34193339-chr6:34210453..34212412,2	MCF-7	breast:
28	chr6:34189603..34191937-chr6:34485538..34487216,2	MCF-7	breast:
29	chr6:34131628..34132318-chr6:34178038..34178559,3	MCF-7	breast:
30	chr12:6976303..6977166-chr6:34191919..34192632,2	Hela-S3	cervix:
31	chr6:34191327..34194039-chr6:34200124..34202308,2	MCF-7	breast:
32	chr6:34160739..34183165-chr6:34199874..34216980,124	K562	blood:
33	chr6:34190610..34193435-chr6:34214728..34218107,4	MCF-7	breast:
34	chr6:34167257..34169586-chr6:34191240..34193285,2	K562	blood:
35	chr6:34180181..34181957-chr6:34360562..34363257,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-HMGA1-4	chr6:34187216-34187482	NONHSAT112113
2	lnc-HMGA1-4	chr6:34187800-34187843	NONHSAT112113

No data

Variant related genes	Relation type
CYCSP55	TF binding region
CYCSP55	CpG island
ENSG00000214810	chromatin interactions
ENSG00000111669	chromatin interactions
ENSG00000124614	chromatin interactions
ENSG00000199347	chromatin interactions
ENSG00000137309	chromatin interactions
ENSG00000270800	chromatin interactions
ENSG00000272325	chromatin interactions
ENSG00000186577	chromatin interactions

Extended variants
information (count: 637 )
Associated
traits (count: 106 )

Variant overlapped rSNPs/rCNVs (count:637 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs561051140	chr6:34177781-34177782	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs148951425	chr6:34177789-34177790	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs543762783	chr6:34177819-34177820	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs185139895	chr6:34177853-34177854	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs9368802	chr6:34177860-34177861	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs369157646	chr6:34177898-34177899	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs533372517	chr6:34177928-34177929	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs190074511	chr6:34177949-34177950	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs113358699	chr6:34178040-34178041	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs371772719	chr6:34178042-34178043	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs373977172	chr6:34178051-34178052	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs551439546	chr6:34178056-34178057	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs560682073	chr6:34178057-34178058	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs138214220	chr6:34178081-34178082	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs111820854	chr6:34178097-34178098	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs74996937	chr6:34178101-34178102	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs528772387	chr6:34178111-34178112	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs115649820	chr6:34178128-34178129	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs182295170	chr6:34178211-34178212	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs9461963	chr6:34178230-34178231	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs386700051	chr6:34178264-34178265	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs79004765	chr6:34178265-34178266	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs553482004	chr6:34178321-34178322	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs572141858	chr6:34178340-34178341	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs186428039	chr6:34178385-34178386	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs554678351	chr6:34178401-34178402	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs576321883	chr6:34178412-34178413	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs188143655	chr6:34178464-34178465	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs565181411	chr6:34178465-34178466	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs180686322	chr6:34178474-34178475	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs370030036	chr6:34178499-34178500	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs185119140	chr6:34178502-34178503	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs373175831	chr6:34178515-34178516	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs10807136	chr6:34178558-34178559	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs138997002	chr6:34178593-34178594	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs191296658	chr6:34178621-34178622	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs551746052	chr6:34178757-34178758	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs28673163	chr6:34178764-34178765	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs561011353	chr6:34178855-34178856	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs531794785	chr6:34178856-34178857	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs549912922	chr6:34178861-34178862	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs571951858	chr6:34178866-34178867	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs181357213	chr6:34178902-34178903	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs547399901	chr6:34178923-34178924	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs28682332	chr6:34178928-34178929	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs536642454	chr6:34178939-34178940	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs565562952	chr6:34179009-34179010	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs536221739	chr6:34179012-34179013	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs376662873	chr6:34179034-34179035	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs554715156	chr6:34179055-34179056	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:106)

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
Urothelial carcinoma	21177765	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
Schizophrenia	23813976	CNVD

Chromatin state (count:377 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:34176000-34180200	Weak transcription	K562	blood
2	chr6:34176200-34190800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
3	chr6:34179200-34179400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
4	chr6:34180200-34180800	Enhancers	K562	blood
5	chr6:34180800-34181200	Weak transcription	K562	blood
6	chr6:34180800-34183000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
7	chr6:34181200-34183000	Enhancers	K562	blood
8	chr6:34183000-34191000	Weak transcription	K562	blood
9	chr6:34184000-34184200	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
10	chr6:34184200-34190000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
11	chr6:34186000-34186800	Enhancers	Primary T cells from cord blood	blood
12	chr6:34186200-34186400	Enhancers	Hela-S3	cervix
13	chr6:34186200-34186800	Enhancers	Primary T helper naive cells from peripheral blood	blood
14	chr6:34186400-34191000	Weak transcription	Hela-S3	cervix
15	chr6:34186800-34191000	Weak transcription	Primary T cells from cord blood	blood
16	chr6:34186800-34191000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
17	chr6:34187200-34187800	Enhancers	Primary B cells from cord blood	blood
18	chr6:34187200-34187800	Enhancers	Primary B cells from peripheral blood	blood
19	chr6:34187800-34188200	Weak transcription	Primary B cells from cord blood	blood
20	chr6:34187800-34188200	Weak transcription	Primary B cells from peripheral blood	blood
21	chr6:34188200-34188400	Enhancers	Primary B cells from cord blood	blood
22	chr6:34188200-34188400	Enhancers	Primary B cells from peripheral blood	blood
23	chr6:34188400-34191000	Weak transcription	Primary B cells from peripheral blood	blood
24	chr6:34188400-34191200	Weak transcription	Primary B cells from cord blood	blood
25	chr6:34189400-34189800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
26	chr6:34189800-34190800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
27	chr6:34190000-34190200	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
28	chr6:34190200-34190600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
29	chr6:34190600-34190800	Enhancers	HUES64 Cell Line	embryonic stem cell
30	chr6:34190600-34190800	Enhancers	iPS-15b Cell Line	embryonic stem cell
31	chr6:34190600-34190800	Enhancers	iPS-20b Cell Line	embryonic stem cell
32	chr6:34190600-34191000	Enhancers	ES-I3 Cell Line	embryonic stem cell
33	chr6:34190600-34191000	Enhancers	H1 Cell Line	embryonic stem cell
34	chr6:34190600-34191000	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
35	chr6:34190600-34191200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
36	chr6:34190800-34191000	Enhancers	HUES48 Cell Line	embryonic stem cell
37	chr6:34190800-34191000	Enhancers	HUES6 Cell Line	embryonic stem cell
38	chr6:34190800-34191000	Enhancers	iPS-18 Cell Line	embryonic stem cell
39	chr6:34190800-34191000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
40	chr6:34190800-34191000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
41	chr6:34190800-34191000	Enhancers	Breast Myoepithelial Primary Cells	Breast
42	chr6:34190800-34191000	Enhancers	Muscle Satellite Cultured Cells	--
43	chr6:34190800-34191000	Enhancers	Brain Angular Gyrus	brain
44	chr6:34190800-34191000	Enhancers	Brain Anterior Caudate	brain
45	chr6:34190800-34191000	Enhancers	Brain Cingulate Gyrus	brain
46	chr6:34190800-34191000	Enhancers	Brain Germinal Matrix	brain
47	chr6:34190800-34191000	Enhancers	Brain Hippocampus Middle	brain
48	chr6:34190800-34191000	Enhancers	Brain Inferior Temporal Lobe	brain
49	chr6:34190800-34191000	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
50	chr6:34190800-34191000	Enhancers	Brain Substantia Nigra	brain

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