Variant report

Variant	nsv884423
Chromosome Location	chr6:31593729-31615167
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:935)
CpG islands
(count:5865)
Chromatin interactive
region (count:23)
LncRNA
region (count:3)
Mature miRNA
region (count: 2)
miRNA target
sites (count:0)

(count:935 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr6:31600723-31600742	K562	blood:	n/a	n/a
2	BCL3	chr6:31605583-31606381	K562	blood:	n/a	n/a
3	BCL3	chr6:31605430-31607366	K562	blood:	n/a	n/a
4	BCLAF1	chr6:31606859-31607316	GM12878	blood:	n/a	n/a
5	BCLAF1	chr6:31605522-31606225	GM12878	blood:	n/a	n/a
6	BCLAF1	chr6:31605529-31605997	K562	blood:	n/a	n/a
7	BHLHE40	chr6:31605726-31605944	K562	blood:	n/a	n/a
8	CCNT2	chr6:31606995-31607060	K562	blood:	n/a	n/a
9	CCNT2	chr6:31599165-31599314	K562	blood:	n/a	n/a
10	CCNT2	chr6:31599555-31599762	K562	blood:	n/a	n/a
11	CCNT2	chr6:31603266-31603362	K562	blood:	n/a	n/a
12	CCNT2	chr6:31601091-31601095	K562	blood:	n/a	n/a
13	CCNT2	chr6:31600588-31600720	K562	blood:	n/a	n/a
14	CEBPB	chr6:31607661-31607907	A549	lung:	n/a	chr6:31607806-31607819 chr6:31607807-31607818
15	CEBPB	chr6:31610967-31611317	HepG2	liver:	n/a	chr6:31611147-31611158
16	CEBPB	chr6:31611004-31611215	HepG2	liver:	n/a	chr6:31611147-31611158
17	CEBPB	chr6:31611043-31611217	HepG2	liver:	n/a	chr6:31611147-31611158
18	CEBPB	chr6:31607668-31607985	HepG2	liver:	n/a	chr6:31607806-31607819 chr6:31607807-31607818
19	CEBPB	chr6:31607723-31607889	K562	blood:	n/a	chr6:31607806-31607819 chr6:31607807-31607818
20	CEBPB	chr6:31607628-31607976	IMR90	lung:	n/a	chr6:31607806-31607819 chr6:31607807-31607818
21	CEBPB	chr6:31610997-31611310	HepG2	liver:	n/a	chr6:31611147-31611158
22	CEBPD	chr6:31605554-31606139	K562	blood:	n/a	n/a
23	CEBPD	chr6:31605478-31606438	K562	blood:	n/a	n/a
24	CHD2	chr6:31603031-31603108	HepG2	liver:	n/a	n/a
25	CHD2	chr6:31600864-31600922	K562	blood:	n/a	n/a
26	CHD2	chr6:31601305-31601519	K562	blood:	n/a	n/a
27	CHD2	chr6:31605782-31605837	K562	blood:	n/a	n/a
28	CHD2	chr6:31605089-31605091	HepG2	liver:	n/a	n/a
29	CHD2	chr6:31600180-31600294	K562	blood:	n/a	n/a
30	CTCF	chr6:31602540-31602690	AG04449	skin:	n/a	n/a
31	CTCF	chr6:31602640-31602790	BJ	skin:	n/a	n/a
32	CTCF	chr6:31602560-31602710	HEK293	kidney:	n/a	n/a
33	CTCF	chr6:31602500-31602650	GM06990	blood:	n/a	n/a
34	CTCF	chr6:31602560-31602710	GM12874	blood:	n/a	n/a
35	CTCF	chr6:31602560-31602710	WERI-Rb-1	eye:	n/a	n/a
36	CTCF	chr6:31611969-31612015	A549	lung:	n/a	n/a
37	CTCF	chr6:31602540-31602690	HCT-116	colon:	n/a	n/a
38	CTCF	chr6:31602580-31602730	HPAF	blood vessel:	n/a	n/a
39	CTCF	chr6:31611880-31612030	MCF-7	breast:	n/a	n/a
40	CTCF	chr6:31602540-31602690	HMF	breast:	n/a	n/a
41	CTCF	chr6:31602540-31602690	GM12865	blood:	n/a	n/a
42	CTCF	chr6:31611740-31611890	HepG2	liver:	n/a	n/a
43	CTCF	chr6:31611900-31612050	HBMEC	blood vessel:	n/a	n/a
44	CTCF	chr6:31611889-31612067	MCF-7	breast:	n/a	n/a
45	CTCF	chr6:31602540-31602690	HCPEpiC	choroid plexus:	n/a	n/a
46	CTCF	chr6:31602580-31602730	HepG2	liver:	n/a	n/a
47	CTCF	chr6:31602560-31602710	HFF-Myc	foreskin:	n/a	n/a
48	CTCF	chr6:31611780-31611930	GM12870	blood:	n/a	n/a
49	CTCF	chr6:31611893-31612053	Hela-S3	cervix:	n/a	n/a
50	CTCF	chr6:31602500-31602650	GM12873	blood:	n/a	n/a

(count:5865 , 50 per page) page: 1 2 3 4 5 6 7 ... 118

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:31607648-31607698	HepG2	liver:	n/a
2	chr6:31597708-31597758	HepG2	liver:	n/a
3	chr6:31603011-31603061	Jurkat	blood:	n/a
4	chr6:31597160-31597210	HPAEpiC	pulmonary alveolar:	n/a
5	chr6:31600558-31600608	SK-N-MC	brain:	n/a
6	chr6:31599631-31599681	GM12892	blood:	n/a
7	chr6:31597580-31597630	HCM	heart:	n/a
8	chr6:31600453-31600503	K562	blood:	n/a
9	chr6:31599520-31599570	HepG2	liver:	n/a
10	chr6:31607648-31607698	HepG2	liver:	n/a
11	chr6:31597708-31597758	HepG2	liver:	n/a
12	chr6:31603011-31603061	Jurkat	blood:	n/a
13	chr6:31597160-31597210	HPAEpiC	pulmonary alveolar:	n/a
14	chr6:31600558-31600608	SK-N-MC	brain:	n/a
15	chr6:31599631-31599681	GM12892	blood:	n/a
16	chr6:31597580-31597630	HCM	heart:	n/a
17	chr6:31600453-31600503	K562	blood:	n/a
18	chr6:31599520-31599570	HepG2	liver:	n/a
19	chr6:31607340-31607390	HRE	kidney:	n/a
20	chr6:31607674-31607724	MCF10A-Er-Src	breast:	n/a
21	chr6:31599289-31599339	Jurkat	blood:	n/a
22	chr6:31600597-31600647	NHDF-neo	bronchial:	n/a
23	chr6:31595945-31595995	PrEC	prostate:	n/a
24	chr6:31599289-31599339	SK-N-SH	brain:	n/a
25	chr6:31607648-31607698	SK-N-MC	brain:	n/a
26	chr6:31601654-31601704	NT2-D1	testis:	n/a
27	chr6:31603535-31603585	HCF	heart:	n/a
28	chr6:31599904-31599954	HIPEpiC	eye:	n/a
29	chr6:31597831-31597881	NB4	blood:	n/a
30	chr6:31598424-31598474	HRPEpiC	eye:	n/a
31	chr6:31600348-31600398	SK-N-MC	brain:	n/a
32	chr6:31599904-31599954	Jurkat	blood:	n/a
33	chr6:31607340-31607390	PANC-1	pancreas:	n/a
34	chr6:31599904-31599954	GM06990	blood:	n/a
35	chr6:31599537-31599587	AG09309	skin:	n/a
36	chr6:31596913-31596963	HRPEpiC	eye:	n/a
37	chr6:31596847-31596897	HRCEpiC	kidney:	n/a
38	chr6:31597160-31597210	NH-A	brain:	n/a
39	chr6:31603476-31603526	HPAEpiC	pulmonary alveolar:	n/a
40	chr6:31599904-31599954	ECC-1	luminal epithelium:	n/a
41	chr6:31599646-31599696	HRCEpiC	kidney:	n/a
42	chr6:31596847-31596897	HCT-116	colon:	n/a
43	chr6:31597160-31597210	AG10803	skin:	n/a
44	chr6:31601226-31601276	HCT-116	colon:	n/a
45	chr6:31601157-31601207	HIPEpiC	eye:	n/a
46	chr6:31598379-31598429	NHDF-neo	bronchial:	n/a
47	chr6:31599532-31599582	HRE	kidney:	n/a
48	chr6:31600180-31600230	HepG2	liver:	n/a
49	chr6:31598424-31598474	HepG2	liver:	n/a
50	chr6:31595725-31595775	NH-A	brain:	n/a

(count:23 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:31601006..31603975-chr6:31604040..31605763,2	MCF-7	breast:
2	chr6:31514041..31516822-chr6:31607895..31609599,2	K562	blood:
3	chr6:31509522..31512324-chr6:31604128..31605952,2	K562	blood:
4	chr6:31507082..31510843-chr6:31599707..31603450,4	K562	blood:
5	chr6:31507710..31510101-chr6:31604073..31606097,3	K562	blood:
6	chr6:31511090..31513028-chr6:31593636..31596148,2	K562	blood:
7	chr6:31612905..31614877-chr6:31621124..31623765,2	MCF-7	breast:
8	chr6:31587269..31589939-chr6:31613609..31618007,4	MCF-7	breast:
9	chr6:31602610..31605344-chr6:31627504..31629558,2	MCF-7	breast:
10	chr6:31513227..31514963-chr6:31602419..31605642,3	K562	blood:
11	chr6:31513469..31517583-chr6:31596741..31599864,5	K562	blood:
12	chr19:11199794..11200296-chr6:31604491..31605393,2	NB4	blood:
13	chr6:31594287..31597004-chr6:31618520..31620536,2	MCF-7	breast:
14	chr6:31601006..31603975-chr6:31604040..31605763,2	MCF-7	breast:
15	chr6:31513697..31516891-chr6:31590663..31594798,6	K562	blood:
16	chr6:31506529..31508833-chr6:31606767..31610616,4	K562	blood:
17	chr6:31586074..31595285-chr6:31626460..31635395,11	MCF-7	breast:
18	chr6:31513053..31519210-chr6:31585987..31595406,29	K562	blood:
19	chr6:31513906..31516898-chr6:31598364..31600133,2	K562	blood:
20	chr6:31594249..31597266-chr6:31695833..31699351,4	MCF-7	breast:
21	chr6:31614786..31617251-chr6:31937528..31940475,2	MCF-7	breast:
22	chr6:31599461..31602010-chr6:31647062..31649518,2	MCF-7	breast:
23	chr6:31610323..31613172-chr6:31793267..31795561,2	MCF-7	breast:

(count:3 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AIF1-3	chr6:31603019-31603049	NONHSAT108803
2	lnc-AIF1-3	chr6:31603171-31603486	NONHSAT108803
3	lnc-C6orf47-2	chr6:31611915-31612240	expReg_chr6_2650_-

miRNA name	Chromosome Location	mirBase accession
hsa-miR-6832-3p	chr6:31601616-31601635	MIMAT0027565
hsa-miR-6832-5p	chr6:31601569-31601591	MIMAT0027564

No data

Variant related genes	Relation type
BAG6	TF binding region
PRRC2A	TF binding region
BAG6	CpG island
PRRC2A	CpG island
ENSG00000234006	chromatin interactions
ENSG00000204388	chromatin interactions
ENSG00000265236	chromatin interactions
ENSG00000204444	chromatin interactions
ENSG00000213760	chromatin interactions
ENSG00000263020	chromatin interactions
ENSG00000201207	chromatin interactions
ENSG00000204498	chromatin interactions
ENSG00000204469	chromatin interactions
ENSG00000204438	chromatin interactions
ENSG00000198563	chromatin interactions
ENSG00000204348	chromatin interactions
ENSG00000213722	chromatin interactions
ENSG00000130164	chromatin interactions
ENSG00000254870	chromatin interactions
ENSG00000204439	chromatin interactions
ENSG00000204463	chromatin interactions
ENSG00000204428	chromatin interactions
ENSG00000204435	chromatin interactions
ENSG00000204344	chromatin interactions

Extended variants
information (count: 1094 )
Associated
traits (count: 133 )

Variant overlapped rSNPs/rCNVs (count:1094 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs372557119	chr6:31593736-31593737	Strong transcription Weak transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
2	rs373572257	chr6:31593748-31593749	Strong transcription Weak transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
3	rs541387961	chr6:31593763-31593764	Strong transcription Weak transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
4	rs200630465	chr6:31593780-31593781	Strong transcription Weak transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
5	rs575401082	chr6:31593798-31593799	Strong transcription Weak transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
6	rs546085889	chr6:31593799-31593800	Strong transcription Weak transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
7	rs368679462	chr6:31593807-31593808	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
8	rs376264291	chr6:31593814-31593815	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
9	rs147717718	chr6:31593815-31593816	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
10	rs370604224	chr6:31593817-31593818	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
11	rs201317702	chr6:31593823-31593824	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
12	rs528285841	chr6:31593840-31593841	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
13	rs34633614	chr6:31593844-31593845	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
14	rs146950774	chr6:31593932-31593933	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
15	rs138104927	chr6:31593950-31593951	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
16	rs377484813	chr6:31593952-31593953	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
17	rs149105624	chr6:31593986-31593987	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
18	rs80219586	chr6:31594054-31594055	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
19	rs533420130	chr6:31594059-31594060	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
20	rs186504243	chr6:31594128-31594129	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
21	rs555613825	chr6:31594154-31594155	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
22	rs2844470	chr6:31594181-31594182	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	9 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
23	rs7751733	chr6:31594222-31594223	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	9 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs181859287	chr6:31594250-31594251	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
25	rs148302854	chr6:31594288-31594289	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
26	rs186928898	chr6:31594289-31594290	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
27	rs556497185	chr6:31594320-31594321	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
28	rs546682422	chr6:31594335-31594336	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
29	rs371120998	chr6:31594348-31594349	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
30	rs142956800	chr6:31594369-31594370	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
31	rs558009840	chr6:31594398-31594399	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
32	rs573088223	chr6:31594415-31594416	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
33	rs111992725	chr6:31594431-31594432	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
34	rs7769995	chr6:31594435-31594436	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	12 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs191359470	chr6:31594483-31594484	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
36	rs529360666	chr6:31594508-31594509	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
37	rs183277052	chr6:31594525-31594526	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
38	rs375095186	chr6:31594556-31594557	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
39	rs3130071	chr6:31594628-31594629	Strong transcription Weak transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region Chromatin interactive region	12 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs185300331	chr6:31594664-31594665	Strong transcription Weak transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
41	rs376815062	chr6:31594667-31594668	Strong transcription Weak transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
42	rs560826659	chr6:31594684-31594685	Strong transcription Weak transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
43	rs549309464	chr6:31594697-31594698	Strong transcription Weak transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
44	rs577305260	chr6:31594747-31594748	Strong transcription Weak transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
45	rs546061995	chr6:31594749-31594750	Strong transcription Weak transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
46	rs111658537	chr6:31594758-31594759	Strong transcription Weak transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
47	rs549116184	chr6:31594764-31594765	Strong transcription Weak transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
48	rs375614423	chr6:31594771-31594772	Strong transcription Weak transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
49	rs201503552	chr6:31594811-31594812	Strong transcription Weak transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
50	rs189765605	chr6:31594840-31594841	Strong transcription Weak transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:133)

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
Lung cancer	18438408	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
Breast cancer	22522925	CNVD
Ovarian cancer	21781307	CNVD
Breast cancer	21552322	CNVD
Immune disease	21076436	CNVD
Autoimmune disease	19135723	CNVD
Systemic lupus erythematosus	17953491	CNVD
Recurrent Infections	22737222	CNVD
Systemic lupus erythematosus	21904924	CNVD
Ependymoma	19289631	CNVD
Breast cancer	22844521	CNVD
Gestational infection	22844521	CNVD
HIV/AIDS	22844521	CNVD
Head circumference	22844521	CNVD
Infertility	22844521	CNVD
Ovarian cancer	22844521	CNVD
Prostate cancer	22844521	CNVD
Psoriasis	22844521	CNVD
Recurrent birth weight diabetes	22844521	CNVD
Rheumatoid arthritis	22844521	CNVD
Sclerosis systemic	22844521	CNVD
Systemic lupus erythematosus	22844521	CNVD
Obesity	22844521	CNVD
Recurrent pregnancy loss	22844521	CNVD
Intellectual disability	21811512	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Congenital anomalies of the kidney and urinary tract	18694510	CNVD
Nasopharyngeal cancer	22815911	CNVD
Hepatocellular carcinoma	16750200	CNVD
Basal cell lymphoma	21115979	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Autism	22495311	CNVD
Cancer	16790693	CNVD
Cervical cancer	21062161	CNVD
Breast cancer	21785460	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
Renal cell carcinoma	18765545	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
abnormal development	18461090	CNVD
Melanoma	17363583	CNVD
Myelofibrosis	22110671	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
Breast cancer	21364760	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
Congenital adrenal hyperplasia	18478071	CNVD
Systemic lupus erythematosus	19287147	CNVD
Osteosarcoma	16790693	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Non-syndromic sensorineural hearing loss	17289997	CNVD
Non-syndromic sensorineural hearing loss	17122850	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
Urothelial carcinoma	21177765	CNVD
Oral cancer	21386901	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:375 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:31589800-31619400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
2	chr6:31590200-31607000	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--
3	chr6:31590200-31617600	Strong transcription	iPS DF 6.9 Cell Line	embryonic stem cell
4	chr6:31590200-31618800	Strong transcription	Primary B cells from peripheral blood	blood
5	chr6:31590400-31617400	Strong transcription	Rectal Smooth Muscle	rectum
6	chr6:31590400-31617600	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
7	chr6:31590400-31618200	Strong transcription	Rectal Mucosa Donor 31	rectum
8	chr6:31590400-31618600	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
9	chr6:31590400-31618600	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
10	chr6:31590400-31618600	Strong transcription	Fetal Intestine Small	intestine
11	chr6:31590600-31598400	Strong transcription	Fetal Muscle Trunk	muscle
12	chr6:31590600-31599400	Strong transcription	Psoas Muscle	Psoas
13	chr6:31590600-31601200	Strong transcription	Primary T cells fromperipheralblood	blood
14	chr6:31590600-31605000	Strong transcription	A549	lung
15	chr6:31590600-31605200	Strong transcription	Primary T helper memory cells from peripheral blood 2	blood
16	chr6:31590600-31606200	Strong transcription	Primary hematopoietic stem cells	blood
17	chr6:31590600-31613200	Strong transcription	ES-I3 Cell Line	embryonic stem cell
18	chr6:31590600-31617200	Strong transcription	Rectal Mucosa Donor 29	rectum
19	chr6:31590600-31617400	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
20	chr6:31590600-31617400	Strong transcription	Right Ventricle	heart
21	chr6:31590600-31617600	Strong transcription	Sigmoid Colon	Sigmoid Colon
22	chr6:31590600-31617800	Strong transcription	H9 Cell Line	embryonic stem cell
23	chr6:31590600-31617800	Strong transcription	Left Ventricle	heart
24	chr6:31590600-31617800	Strong transcription	Thymus	Thymus
25	chr6:31590600-31618000	Strong transcription	Fetal Lung	lung
26	chr6:31590600-31618600	Strong transcription	H1 Cell Line	embryonic stem cell
27	chr6:31590600-31618600	Strong transcription	Primary hematopoietic stem cells short term culture	blood
28	chr6:31590600-31618800	Strong transcription	Fetal Stomach	stomach
29	chr6:31590800-31598800	Strong transcription	HSMM	muscle
30	chr6:31590800-31599600	Strong transcription	Primary T killer memory cells from peripheral blood	blood
31	chr6:31590800-31600600	Strong transcription	Liver	Liver
32	chr6:31590800-31602200	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
33	chr6:31590800-31604600	Strong transcription	Fetal Muscle Leg	muscle
34	chr6:31590800-31605600	Strong transcription	Skeletal Muscle Male	skeletal muscle
35	chr6:31590800-31607000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
36	chr6:31590800-31607000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
37	chr6:31590800-31607200	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
38	chr6:31590800-31609200	Strong transcription	Brain Anterior Caudate	brain
39	chr6:31590800-31617400	Strong transcription	Stomach Smooth Muscle	stomach
40	chr6:31590800-31617600	Strong transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
41	chr6:31590800-31617800	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
42	chr6:31590800-31617800	Strong transcription	Duodenum Mucosa	Duodenum
43	chr6:31590800-31618400	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
44	chr6:31590800-31618400	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
45	chr6:31590800-31618600	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
46	chr6:31590800-31618600	Strong transcription	HUES64 Cell Line	embryonic stem cell
47	chr6:31590800-31618600	Strong transcription	iPS-18 Cell Line	embryonic stem cell
48	chr6:31590800-31618600	Strong transcription	iPS-20b Cell Line	embryonic stem cell
49	chr6:31590800-31618800	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
50	chr6:31590800-31619000	Strong transcription	HUES48 Cell Line	embryonic stem cell

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