Variant report

Variant	esv3388703
Chromosome Location	chr6:163833387-163836135
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:700)
CpG islands
(count:610)
Chromatin interactive
region (count:10)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:700 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:163834674-163835193	K562	blood:	n/a	n/a
2	ARID3A	chr6:163833393-163835195	HepG2	liver:	n/a	n/a
3	ATF1	chr6:163833475-163833658	K562	blood:	n/a	n/a
4	ATF2	chr6:163834078-163834503	GM12878	blood:	n/a	n/a
5	ATF2	chr6:163833939-163834675	GM12878	blood:	n/a	n/a
6	ATF2	chr6:163834922-163835269	GM12878	blood:	n/a	n/a
7	ATF2	chr6:163834688-163835329	GM12878	blood:	n/a	n/a
8	ATF3	chr6:163834850-163835290	GM12878	blood:	n/a	n/a
9	ATF3	chr6:163835011-163835162	GM12878	blood:	n/a	n/a
10	ATF3	chr6:163834928-163835250	K562	blood:	n/a	n/a
11	ATF3	chr6:163834927-163835263	H1-hESC	embryonic stem cell:	n/a	n/a
12	ATF3	chr6:163834976-163835190	H1-hESC	embryonic stem cell:	n/a	n/a
13	ATF3	chr6:163834904-163835255	HepG2	liver:	n/a	n/a
14	ATF3	chr6:163834816-163835317	HepG2	liver:	n/a	n/a
15	ATF3	chr6:163834497-163834859	K562	blood:	n/a	n/a
16	BACH1	chr6:163834314-163835318	H1-hESC	embryonic stem cell:	n/a	n/a
17	BACH1	chr6:163833884-163835210	K562	blood:	n/a	n/a
18	BCLAF1	chr6:163834193-163835293	GM12878	blood:	n/a	chr6:163834831-163834840
19	BCLAF1	chr6:163834461-163835301	K562	blood:	n/a	chr6:163834831-163834840 chr6:163835287-163835300
20	BCLAF1	chr6:163835600-163835941	GM12878	blood:	n/a	chr6:163835760-163835773 chr6:163835781-163835790 chr6:163835779-163835792
21	BCLAF1	chr6:163834227-163835276	GM12878	blood:	n/a	chr6:163834831-163834840
22	BHLHE40	chr6:163834536-163834943	A549	lung:	n/a	n/a
23	BHLHE40	chr6:163835608-163835832	GM12878	blood:	n/a	chr6:163835760-163835776 chr6:163835757-163835773
24	BHLHE40	chr6:163835658-163835902	K562	blood:	n/a	chr6:163835760-163835776 chr6:163835757-163835773
25	BHLHE40	chr6:163834242-163835307	K562	blood:	n/a	n/a
26	BHLHE40	chr6:163833621-163835329	GM12878	blood:	n/a	n/a
27	BHLHE40	chr6:163834344-163835354	HepG2	liver:	n/a	n/a
28	BRCA1	chr6:163834833-163835219	GM12878	blood:	n/a	n/a
29	BRCA1	chr6:163834883-163835128	HepG2	liver:	n/a	n/a
30	BRCA1	chr6:163834975-163835254	Hela-S3	cervix:	n/a	n/a
31	CBX3	chr6:163834088-163835319	K562	blood:	n/a	n/a
32	CBX3	chr6:163834516-163834893	K562	blood:	n/a	n/a
33	CCNT2	chr6:163833862-163837213	K562	blood:	n/a	chr6:163837081-163837090
34	CEBPB	chr6:163834963-163835288	A549	lung:	n/a	n/a
35	CEBPB	chr6:163834971-163835239	HepG2	liver:	n/a	n/a
36	CEBPB	chr6:163835037-163835191	H1-hESC	embryonic stem cell:	n/a	n/a
37	CEBPB	chr6:163833837-163834672	HepG2	liver:	n/a	n/a
38	CEBPB	chr6:163834232-163835874	HepG2	liver:	n/a	n/a
39	CEBPB	chr6:163834965-163835311	Hela-S3	cervix:	n/a	n/a
40	CEBPB	chr6:163834947-163835336	IMR90	lung:	n/a	n/a
41	CEBPB	chr6:163834959-163835331	A549	lung:	n/a	n/a
42	CEBPB	chr6:163833449-163834753	K562	blood:	n/a	n/a
43	CEBPB	chr6:163834953-163835326	K562	blood:	n/a	n/a
44	CEBPB	chr6:163834962-163835251	K562	blood:	n/a	n/a
45	CEBPB	chr6:163834950-163835319	HepG2	liver:	n/a	n/a
46	CEBPD	chr6:163835562-163836037	HepG2	liver:	n/a	n/a
47	CEBPD	chr6:163834632-163835556	HepG2	liver:	n/a	n/a
48	CEBPD	chr6:163834681-163835222	HepG2	liver:	n/a	n/a
49	CEBPD	chr6:163834692-163835178	K562	blood:	n/a	n/a
50	CHD1	chr6:163835594-163839152	IMR90	lung:	n/a	n/a

(count:610 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:163834924-163834974	HRPEpiC	eye:	n/a
2	chr6:163834176-163834226	GM12891	blood:	n/a
3	chr6:163835251-163835301	HL-60	blood:	n/a
4	chr6:163835395-163835445	SK-N-SH	brain:	n/a
5	chr6:163835117-163835167	HRCEpiC	kidney:	n/a
6	chr6:163835251-163835301	NH-A	brain:	n/a
7	chr6:163834924-163834974	HRCEpiC	kidney:	n/a
8	chr6:163835395-163835445	HUVEC	blood vessel:	n/a
9	chr6:163835117-163835167	AG09319	gingival:	n/a
10	chr6:163834924-163834974	IMR90	lung:	fetal
11	chr6:163834158-163834208	CMK	blood:	n/a
12	chr6:163835251-163835301	Jurkat	blood:	n/a
13	chr6:163834903-163834953	AoSMC	blood vessel:	n/a
14	chr6:163835582-163835632	ECC-1	luminal epithelium:	n/a
15	chr6:163834872-163834922	Hela-S3	cervix:	n/a
16	chr6:163835582-163835632	A549	lung:	n/a
17	chr6:163834924-163834974	GM19239	blood:	n/a
18	chr6:163835395-163835445	GM12891	blood:	n/a
19	chr6:163834176-163834226	AG04450	lung:	fetal
20	chr6:163835251-163835301	SAEC	small airway:	n/a
21	chr6:163835117-163835167	HL-60	blood:	n/a
22	chr6:163835395-163835445	Caco-2	colon:	n/a
23	chr6:163834872-163834922	BJ	skin:	n/a
24	chr6:163834924-163834974	NH-A	brain:	n/a
25	chr6:163835117-163835167	HNPCEpiC	eye:	n/a
26	chr6:163834176-163834226	HepG2	liver:	n/a
27	chr6:163834924-163834974	SK-N-SH_RA	brain:	n/a
28	chr6:163835251-163835301	NHDF-neo	bronchial:	n/a
29	chr6:163834176-163834226	NT2-D1	testis:	n/a
30	chr6:163834872-163834922	K562	blood:	n/a
31	chr6:163834872-163834922	SK-N-SH_RA	brain:	n/a
32	chr6:163834924-163834974	NHDF-neo	bronchial:	n/a
33	chr6:163835582-163835632	GM12892	blood:	n/a
34	chr6:163834176-163834226	MCF10A-Er-Src	breast:	n/a
35	chr6:163834158-163834208	HAEpiC	amniotic membrane:	n/a
36	chr6:163834158-163834208	NHBE	bronchial:	n/a
37	chr6:163834452-163834502	PFSK-1	brain:	n/a
38	chr6:163835582-163835632	H1-hESC	embryonic stem cell:	embryo
39	chr6:163834176-163834226	CMK	blood:	n/a
40	chr6:163834924-163834974	HIPEpiC	eye:	n/a
41	chr6:163835251-163835301	HEEpiC	esophagus:	n/a
42	chr6:163835251-163835301	K562	blood:	n/a
43	chr6:163835395-163835445	PrEC	prostate:	n/a
44	chr6:163835117-163835167	HepG2	liver:	n/a
45	chr6:163835251-163835301	Hepatocyte	liver:	n/a
46	chr6:163834158-163834208	IMR90	lung:	fetal
47	chr6:163834924-163834974	T-47D	breast:	n/a
48	chr6:163834176-163834226	NH-A	brain:	n/a
49	chr6:163834872-163834922	AG10803	skin:	n/a
50	chr6:163834872-163834922	IMR90	lung:	fetal

(count:10 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:163832712..163834333-chr6:164408971..164410917,2	K562	blood:
2	chr6:163707215..163709135-chr6:163832836..163834940,2	MCF-7	breast:
3	chr6:163834433..163837014-chr6:163986395..163988827,2	K562	blood:
4	chr6:163833988..163836212-chr6:163848529..163850044,2	MCF-7	breast:
5	chr5:34007852..34008601-chr6:163834316..163835107,2	Hela-S3	cervix:
6	chr6:163680711..163682973-chr6:163830679..163833543,2	K562	blood:
7	chr6:163832850..163838270-chr6:163950827..163956360,5	K562	blood:
8	chr6:163831740..163833588-chr6:164102782..164105266,2	K562	blood:
9	chr6:163725918..163727720-chr6:163831906..163834070,2	K562	blood:
10	chr17:8075909..8076789-chr6:163834187..163834895,2	Hela-S3	cervix:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-QKI-6	chr6:163833646-163833771	NONHSAT115961

No data

Variant related genes	Relation type
CAHM	TF binding region
QKI	TF binding region
CAHM	CpG island
QKI	CpG island
ENSG00000112531	chromatin interactions
ENSG00000242110	chromatin interactions

Extended variants
information (count: 93 )
Associated
traits (count: 87 )

Variant overlapped rSNPs/rCNVs (count:93 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs183665852	chr6:163833434-163833435	Active TSS Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs562929030	chr6:163833436-163833437	Active TSS Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs76658962	chr6:163833446-163833447	Active TSS Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs546197285	chr6:163833449-163833450	Active TSS Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs561709415	chr6:163833500-163833501	Active TSS Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs372490761	chr6:163833524-163833525	Active TSS Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs2784865	chr6:163833535-163833536	Active TSS Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
8	rs367888242	chr6:163833551-163833552	Active TSS Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs140751713	chr6:163833563-163833564	Active TSS Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs539003138	chr6:163833566-163833567	Active TSS Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs144624465	chr6:163833568-163833569	Active TSS Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs569353366	chr6:163833582-163833583	Active TSS Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs528901297	chr6:163833602-163833603	Active TSS Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs61407976	chr6:163833609-163833610	Active TSS Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs3857504	chr6:163833610-163833611	Active TSS Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
16	rs146762380	chr6:163833612-163833613	Active TSS Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs61385143	chr6:163833671-163833672	Active TSS Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
18	rs147863667	chr6:163833698-163833699	Active TSS Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
19	rs116737180	chr6:163833703-163833704	Active TSS Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
20	rs182205741	chr6:163833717-163833718	Active TSS Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
21	rs576291870	chr6:163833745-163833746	Active TSS Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
22	rs140074751	chr6:163833777-163833778	Active TSS Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs373449640	chr6:163833831-163833832	Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs34367606	chr6:163833868-163833869	Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs141668582	chr6:163833919-163833920	Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs554122316	chr6:163833927-163833928	Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs201296387	chr6:163833940-163833941	Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs375721238	chr6:163833941-163833942	Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs577621415	chr6:163833959-163833960	Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs546560300	chr6:163833970-163833971	Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs562864010	chr6:163833971-163833972	Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs73244749	chr6:163834006-163834007	Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs369962945	chr6:163834107-163834108	Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs113717867	chr6:163834113-163834114	Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs562225159	chr6:163834117-163834118	Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs532862483	chr6:163834124-163834125	Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs73013596	chr6:163834157-163834158	Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs151203705	chr6:163834232-163834233	Active TSS Bivalent/Poised TSS Flanking Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs564187821	chr6:163834247-163834248	Active TSS Bivalent/Poised TSS Flanking Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs533051591	chr6:163834261-163834262	Active TSS Bivalent/Poised TSS Flanking Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs549712105	chr6:163834306-163834307	Active TSS Bivalent/Poised TSS Flanking Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs187174998	chr6:163834308-163834309	Active TSS Bivalent/Poised TSS Flanking Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs569786899	chr6:163834326-163834327	Active TSS Bivalent/Poised TSS Flanking Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs535116045	chr6:163834333-163834334	Active TSS Bivalent/Poised TSS Flanking Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs548773798	chr6:163834360-163834361	Active TSS Bivalent/Poised TSS Flanking Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs192477025	chr6:163834374-163834375	Active TSS Bivalent/Poised TSS Flanking Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs181490435	chr6:163834384-163834385	Active TSS Bivalent/Poised TSS Flanking Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs554333887	chr6:163834407-163834408	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs373888063	chr6:163834435-163834436	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs547161027	chr6:163834444-163834445	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:87)

Disease	PMID	Source
Uveal melanoma	21693616	CNVD
Glioblastoma multiforme	21080181	CNVD
Biliary cancer	19435499	CNVD
Medulloblastoma	21979893	CNVD
Malaria	21533027	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Ewing''s sarcoma	17952124	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Neuroblastoma	18923191	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Melanoma	18172304	CNVD
Cancer	21637783	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Follicular lymphoma	19010834	CNVD
Non-small cell lung cancer	21044232	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	16608533	CNVD
Non-small cell lung cancer	21385341	CNVD
Prostate cancer	16705090	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Colorectal cancer	16272173	CNVD
Ependymoma	16718352	CNVD
Gastric cancer	17908304	CNVD
High-proliferative meningiomas	17937814	CNVD
Intracranial tumor	16823260	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	16272173	CNVD
Wilms tumour	21544195	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Malignant melanoma	18718029	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Breast cancer	21858162	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	17603634	CNVD
Developmental delay	19490664	CNVD
Burkitt''s lymphoma	18698080	CNVD
Neurodevelopmental disorder	22521361	CNVD
small cell lung cancer	20016488	CNVD
Adenoid cystic carcinoma	18698036	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Leukemia	18688285	CNVD
Renal cell carcinoma	18592004	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Prostate cancer	18632612	CNVD
Lung cancer	18438408	CNVD
Burkitt''s lymphoma	19759907	CNVD
Esophageal cancer	21851588	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Breast cancer	17133270	CNVD
Testicular germ cell tumor	18059402	CNVD
Developmental delay	21147756	CNVD
Chordoma	18071362	CNVD
Myelofibrosis	22110671	CNVD
Autism	22241247	CNVD
Breast cancer	16397240	CNVD
Atherosclerosis	21956041	CNVD
Maculopathy	20981449	CNVD
Retinoblastoma	22278416	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Ovarian cancer	20844748	CNVD
Uveal melanoma	20484589	CNVD
Glioblastoma multiforme	19435819	CNVD
Astrocytoma	16205629	CNVD
Parkinson disease	17160897	CNVD
Ovarian cancer	21720365	CNVD
Glioblastoma multiforme	21138945	CNVD
Ovarian cancer	22355333	CNVD
abnormal development	18461090	CNVD
Breast cancer	22522925	CNVD
Epilepsy	22083797	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:347 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:163827200-163833600	Weak transcription	H1 Cell Line	embryonic stem cell
2	chr6:163827200-163833600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
3	chr6:163827200-163833800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr6:163827200-163834200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
5	chr6:163827200-163834200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
6	chr6:163827200-163834200	Weak transcription	Spleen	Spleen
7	chr6:163827400-163833400	Weak transcription	HSMM	muscle
8	chr6:163827400-163833600	Weak transcription	Psoas Muscle	Psoas
9	chr6:163827400-163833600	Weak transcription	Right Atrium	heart
10	chr6:163827400-163833800	Weak transcription	Aorta	Aorta
11	chr6:163827600-163833400	Weak transcription	HUES6 Cell Line	embryonic stem cell
12	chr6:163827600-163833400	Weak transcription	HUES64 Cell Line	embryonic stem cell
13	chr6:163827600-163833400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
14	chr6:163827600-163833400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
15	chr6:163827600-163833400	Weak transcription	Fetal Lung	lung
16	chr6:163827600-163833400	Weak transcription	Fetal Stomach	stomach
17	chr6:163827600-163833400	Weak transcription	NHLF	lung
18	chr6:163827600-163833800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
19	chr6:163827800-163833400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
20	chr6:163827800-163833400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
21	chr6:163827800-163833400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
22	chr6:163827800-163833400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
23	chr6:163827800-163833400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
24	chr6:163828000-163833600	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
25	chr6:163828200-163833400	Weak transcription	Liver	Liver
26	chr6:163828200-163833400	Weak transcription	Duodenum Smooth Muscle	Duodenum
27	chr6:163828200-163833400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
28	chr6:163828200-163833400	Weak transcription	Right Ventricle	heart
29	chr6:163828200-163833400	Weak transcription	GM12878-XiMat	blood
30	chr6:163828200-163833600	Weak transcription	Primary T helper cells fromperipheralblood	blood
31	chr6:163828800-163833400	Weak transcription	NHDF-Ad	bronchial
32	chr6:163830600-163833600	Weak transcription	Pancreatic Islets	Pancreatic Islet
33	chr6:163831200-163833400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
34	chr6:163831200-163833400	Enhancers	HepG2	liver
35	chr6:163831200-163834200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
36	chr6:163832400-163833400	Enhancers	Primary monocytes fromperipheralblood	blood
37	chr6:163832600-163833400	Enhancers	Primary B cells from cord blood	blood
38	chr6:163832600-163833400	Enhancers	Primary hematopoietic stem cells	blood
39	chr6:163832600-163833400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
40	chr6:163832600-163833400	Weak transcription	Muscle Satellite Cultured Cells	--
41	chr6:163832600-163833400	Weak transcription	Brain Angular Gyrus	brain
42	chr6:163832600-163833400	Weak transcription	Brain Germinal Matrix	brain
43	chr6:163832600-163833400	Weak transcription	Brain Substantia Nigra	brain
44	chr6:163832600-163833400	Weak transcription	Osteobl	bone
45	chr6:163832600-163834000	Weak transcription	Lung	lung
46	chr6:163832600-163834200	Weak transcription	Gastric	stomach
47	chr6:163832600-163841400	Active TSS	Skeletal Muscle Male	skeletal muscle
48	chr6:163832800-163833400	Weak transcription	HUES48 Cell Line	embryonic stem cell
49	chr6:163832800-163833400	Weak transcription	Skeletal Muscle Female	skeletal muscle
50	chr6:163832800-163833600	Weak transcription	Placenta	Placenta

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