Variant report

Variant	nsv884521
Chromosome Location	chr6:31941767-32010262
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:799)
CpG islands
(count:3543)
Chromatin interactive
region (count:26)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:2)

(count:799 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:31947365-31947781	K562	blood:	n/a	n/a
2	BHLHE40	chr6:31970701-31971047	HepG2	liver:	n/a	n/a
3	BHLHE40	chr6:32003438-32003784	HepG2	liver:	n/a	n/a
4	BHLHE40	chr6:31949559-31949880	HepG2	liver:	n/a	n/a
5	BHLHE40	chr6:32007706-32008062	HepG2	liver:	n/a	n/a
6	BHLHE40	chr6:31947116-31947502	K562	blood:	n/a	n/a
7	BHLHE40	chr6:31982297-31982618	HepG2	liver:	n/a	n/a
8	CBX3	chr6:31957963-31958493	K562	blood:	n/a	n/a
9	CBX3	chr6:31952793-31953135	K562	blood:	n/a	n/a
10	CBX3	chr6:31990712-31991199	K562	blood:	n/a	n/a
11	CBX3	chr6:31965417-31965721	K562	blood:	n/a	n/a
12	CBX3	chr6:31980155-31981063	K562	blood:	n/a	n/a
13	CBX3	chr6:31970603-31971015	K562	blood:	n/a	n/a
14	CBX3	chr6:31958022-31958441	K562	blood:	n/a	n/a
15	CBX3	chr6:31982302-31982628	K562	blood:	n/a	n/a
16	CBX3	chr6:31989920-31990157	K562	blood:	n/a	n/a
17	CBX3	chr6:31970387-31971162	K562	blood:	n/a	n/a
18	CBX3	chr6:32003387-32003757	K562	blood:	n/a	n/a
19	CBX3	chr6:32003260-32004138	K562	blood:	n/a	n/a
20	CBX3	chr6:31985480-31985931	K562	blood:	n/a	n/a
21	CBX3	chr6:31985535-31985921	K562	blood:	n/a	n/a
22	CBX3	chr6:31946996-31947474	K562	blood:	n/a	n/a
23	CBX3	chr6:31952664-31953239	K562	blood:	n/a	n/a
24	CBX3	chr6:31989858-31990273	K562	blood:	n/a	n/a
25	CBX3	chr6:31990799-31991208	K562	blood:	n/a	n/a
26	CCNT2	chr6:31947256-31947610	K562	blood:	n/a	n/a
27	CEBPB	chr6:32003420-32003920	K562	blood:	n/a	n/a
28	CEBPB	chr6:31970725-31971176	K562	blood:	n/a	n/a
29	CEBPB	chr6:31970574-31971273	K562	blood:	n/a	n/a
30	CEBPB	chr6:32003276-32004129	K562	blood:	n/a	n/a
31	CEBPD	chr6:31980664-31980987	K562	blood:	n/a	n/a
32	CEBPD	chr6:31970600-31971236	K562	blood:	n/a	n/a
33	CEBPD	chr6:32003343-32003982	K562	blood:	n/a	n/a
34	CEBPD	chr6:31972233-31972447	HepG2	liver:	n/a	n/a
35	CHD2	chr6:31947206-31947389	K562	blood:	n/a	n/a
36	CTCF	chr6:31990010-31990190	Kidney_OC	kidney:	n/a	n/a
37	CTCF	chr6:31962371-31962431	GM10248	blood:	n/a	n/a
38	CTCF	chr6:31975120-31975270	HCPEpiC	choroid plexus:	n/a	n/a
39	CTCF	chr6:32006160-32006257	MCF-7	breast:	n/a	n/a
40	CTCF	chr6:31972451-31972500	GM20000	blood:	n/a	n/a
41	CTCF	chr6:32007726-32007926	HepG2	liver:	n/a	n/a
42	CTCF	chr6:31957355-31957374	Spleen_OC	spleen:	n/a	n/a
43	CTCF	chr6:31990002-31990111	A549	lung:	n/a	n/a
44	CTCF	chr6:31976010-31976131	Hela-S3	cervix:	n/a	n/a
45	CTCF	chr6:31973400-31973550	SAEC	small airway:	n/a	n/a
46	CTCF	chr6:32007860-32008010	HepG2	liver:	n/a	n/a
47	CTCF	chr6:31957276-31957380	Fibrobl	skin:	n/a	n/a
48	CTCF	chr6:31973400-31973550	HEK293	kidney:	n/a	n/a
49	CTCF	chr6:32006197-32006263	MCF-7	breast:	n/a	n/a
50	CTCF	chr6:31957591-31957672	MCF-7	breast:	n/a	n/a

(count:3543 , 50 per page) page: 1 2 3 4 5 6 7 ... 71

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:31976548-31976598	A549	lung:	n/a
2	chr6:31943512-31943562	HL-60	blood:	n/a
3	chr6:31980856-31980906	GM12891	blood:	n/a
4	chr6:31996931-31996981	Jurkat	blood:	n/a
5	chr6:31943267-31943317	GM12892	blood:	n/a
6	chr6:31976548-31976598	A549	lung:	n/a
7	chr6:31943512-31943562	HL-60	blood:	n/a
8	chr6:31980856-31980906	GM12891	blood:	n/a
9	chr6:31996931-31996981	Jurkat	blood:	n/a
10	chr6:31943267-31943317	GM12892	blood:	n/a
11	chr6:31980046-31980096	K562	blood:	n/a
12	chr6:31973255-31973305	RPTEC	kidney:	n/a
13	chr6:31997067-31997117	SK-N-MC	brain:	n/a
14	chr6:32005786-32005836	PFSK-1	brain:	n/a
15	chr6:31943512-31943562	NHDF-neo	bronchial:	n/a
16	chr6:31964288-31964338	ProgFib	skin:	n/a
17	chr6:31977506-31977556	AG04450	lung:	fetal
18	chr6:32007642-32007692	ProgFib	skin:	n/a
19	chr6:31980052-31980102	AG09319	gingival:	n/a
20	chr6:31947212-31947262	NT2-D1	testis:	n/a
21	chr6:31980052-31980102	LNCaP	prostate:	n/a
22	chr6:31964315-31964365	ProgFib	skin:	n/a
23	chr6:32009283-32009333	PFSK-1	brain:	n/a
24	chr6:31964754-31964804	HAEpiC	amniotic membrane:	n/a
25	chr6:31996657-31996707	RPTEC	kidney:	n/a
26	chr6:31943273-31943323	HRE	kidney:	n/a
27	chr6:31977443-31977493	A549	lung:	n/a
28	chr6:31997059-31997109	LNCaP	prostate:	n/a
29	chr6:31964193-31964243	HCF	heart:	n/a
30	chr6:31976687-31976737	AoSMC	blood vessel:	n/a
31	chr6:32009283-32009333	Caco-2	colon:	n/a
32	chr6:31973051-31973101	U87	brain:	n/a
33	chr6:31977506-31977556	GM06990	blood:	n/a
34	chr6:31947212-31947262	A549	lung:	n/a
35	chr6:31973051-31973101	Hepatocyte	liver:	n/a
36	chr6:31943267-31943317	RPTEC	kidney:	n/a
37	chr6:31978789-31978839	HIPEpiC	eye:	n/a
38	chr6:31978789-31978839	HEEpiC	esophagus:	n/a
39	chr6:31964391-31964441	AG04449	skin:	fetal
40	chr6:32005786-32005836	GM06990	blood:	n/a
41	chr6:31964288-31964338	HNPCEpiC	eye:	n/a
42	chr6:31980845-31980895	PANC-1	pancreas:	n/a
43	chr6:31980043-31980093	Jurkat	blood:	n/a
44	chr6:31977599-31977649	HAEpiC	amniotic membrane:	n/a
45	chr6:31944187-31944237	SK-N-MC	brain:	n/a
46	chr6:31944187-31944237	U87	brain:	n/a
47	chr6:31997564-31997614	NHDF-neo	bronchial:	n/a
48	chr6:31973180-31973230	HRCEpiC	kidney:	n/a
49	chr6:32007916-32007966	GM12878	blood:	n/a
50	chr6:31943512-31943562	NT2-D1	testis:	n/a

(count:26 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:31938465..31944613-chr6:32012205..32018958,7	K562	blood:
2	chr6:31758779..31760923-chr6:31939769..31942169,2	K562	blood:
3	chr6:31942872..31944995-chr6:31945602..31947242,2	MCF-7	breast:
4	chr6:31942872..31944995-chr6:31945602..31947242,2	MCF-7	breast:
5	chr6:31801345..31802956-chr6:31941361..31943630,2	K562	blood:
6	chr6:31763649..31765429-chr6:31938517..31942129,4	K562	blood:
7	chr6:31508285..31510798-chr6:31940056..31942252,2	K562	blood:
8	chr6:31697890..31700450-chr6:31939330..31941948,2	K562	blood:
9	chr6:31830500..31832979-chr6:31939876..31941891,3	K562	blood:
10	chr6:31935647..31937211-chr6:31946410..31948036,2	K562	blood:
11	chr6:31912743..31916758-chr6:31944927..31949257,3	K562	blood:
12	chr6:31938785..31941869-chr6:32936192..32938386,3	MCF-7	breast:
13	chr6:31937794..31943427-chr6:31944150..31949640,18	K562	blood:
14	chr6:31830505..31832934-chr6:31940391..31942572,2	K562	blood:
15	chr6:31631495..31634660-chr6:31935613..31943206,9	K562	blood:
16	chr6:31938987..31942159-chr6:31944563..31949146,6	MCF-7	breast:
17	chr6:31938987..31942159-chr6:31944563..31949146,6	MCF-7	breast:
18	chr6:31868623..31870778-chr6:31945874..31948322,2	K562	blood:
19	chr6:31867614..31871926-chr6:31937988..31942087,9	K562	blood:
20	chr6:31507859..31509785-chr6:31940752..31943113,2	K562	blood:
21	chr6:31743176..31746587-chr6:31939802..31942689,4	K562	blood:
22	chr6:31868706..31872478-chr6:31938286..31942065,5	MCF-7	breast:
23	chr6:31939757..31942101-chr6:31945170..31946681,2	MCF-7	breast:
24	chr6:31937794..31943427-chr6:31944150..31949640,18	K562	blood:
25	chr6:31863628..31867852-chr6:31937946..31941812,10	MCF-7	breast:
26	chr6:31864068..31872693-chr6:31934470..31941847,12	MCF-7	breast:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-DOM3Z-2	chr6:31967753-31969345	ENSG00000233627.2
2	lnc-TNXB-6	chr6:32003534-32004035	ENSG00000229776.1
3	lnc-DOM3Z-2	chr6:31970797-31971298	ENSG00000233627.2
4	lnc-TNXB-6	chr6:32000490-32002082	ENSG00000229776.1

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	STK19	hsa-miR-29c-3p	chr6:31981823-31981843
2	STK19	hsa-miR-29c-3p	chr6:31949085-31949105

Variant related genes	Relation type
TNXA	TF binding region
STK19P	TF binding region
CYP21A1P	TF binding region
C4B	TF binding region
C4B-AS1	TF binding region
DXO	TF binding region
CYP21A2	TF binding region
STK19	TF binding region
ENSG00000268923	TF binding region
C4A-AS1	TF binding region
C4A	TF binding region
TNXA	CpG island
STK19P	CpG island
CYP21A1P	CpG island
C4B	CpG island
C4B-AS1	CpG island
DXO	CpG island
CYP21A2	CpG island
STK19	CpG island
ENSG00000268923	CpG island
C4A-AS1	CpG island
C4A	CpG island
ENSG00000204387	chromatin interactions
ENSG00000198563	chromatin interactions
ENSG00000204435	chromatin interactions
ENSG00000204348	chromatin interactions
ENSG00000204386	chromatin interactions
ENSG00000263020	chromatin interactions
ENSG00000204366	chromatin interactions
ENSG00000204396	chromatin interactions
ENSG00000204371	chromatin interactions
ENSG00000204438	chromatin interactions
ENSG00000166278	chromatin interactions
ENSG00000204257	chromatin interactions
ENSG00000213722	chromatin interactions
ENSG00000204394	chromatin interactions
ENSG00000168477	chromatin interactions
ENSG00000243649	chromatin interactions
ENSG00000204344	chromatin interactions
ENSG00000204385	chromatin interactions
ENSG00000204256	chromatin interactions
ENSG00000204351	chromatin interactions
ENSG00000265236	chromatin interactions
ENSG00000234006	chromatin interactions
ENSG00000223837	chromatin interactions

Extended variants
information (count: 1179 )
Associated
traits (count: 137 )

Variant overlapped rSNPs/rCNVs (count:1179 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs55633728	chr6:31941767-31941768	Weak transcription Enhancers Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	21 gene(s)	Overlapped CNVs	n/a
2	rs2284179	chr6:31941891-31941892	Weak transcription Enhancers Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	17 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs572896294	chr6:31941904-31941905	Weak transcription Enhancers Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	17 gene(s)	Overlapped CNVs	n/a
4	rs539802744	chr6:31941970-31941971	Weak transcription Enhancers Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	16 gene(s)	Overlapped CNVs	n/a
5	rs114695784	chr6:31942016-31942017	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	16 gene(s)	Overlapped CNVs	n/a
6	rs543182385	chr6:31942057-31942058	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	16 gene(s)	Overlapped CNVs	n/a
7	rs11404431	chr6:31942075-31942076	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	16 gene(s)	Overlapped CNVs	n/a
8	rs528844112	chr6:31942149-31942150	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
9	rs550679985	chr6:31942171-31942172	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
10	rs550487303	chr6:31942521-31942522	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers	Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
11	rs180745878	chr6:31942550-31942551	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers	Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
12	rs537667450	chr6:31942557-31942558	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers	Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
13	rs55712638	chr6:31942732-31942733	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
14	rs533017897	chr6:31942752-31942753	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
15	rs551852142	chr6:31942810-31942811	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
16	rs534300566	chr6:31942933-31942934	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
17	rs141346672	chr6:31943008-31943009	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
18	rs567685785	chr6:31943010-31943011	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
19	rs186003115	chr6:31943035-31943036	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
20	rs556932520	chr6:31943066-31943067	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
21	rs578117850	chr6:31943128-31943129	Weak transcription Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
22	rs538809404	chr6:31943170-31943171	Weak transcription Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
23	rs189913727	chr6:31943206-31943207	Weak transcription ZNF genes & repeats Strong transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
24	rs41315812	chr6:31943232-31943233	Weak transcription ZNF genes & repeats Strong transcription	TF binding region Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs376438222	chr6:31943267-31943268	Weak transcription ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
26	rs139246408	chr6:31943268-31943269	Weak transcription ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
27	rs182507103	chr6:31943299-31943300	Weak transcription ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
28	rs573333973	chr6:31943327-31943328	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs113799993	chr6:31943335-31943336	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs149975056	chr6:31943363-31943364	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs545393101	chr6:31943419-31943420	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs571166373	chr6:31943436-31943437	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs562689172	chr6:31943452-31943453	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs533262984	chr6:31943515-31943516	Weak transcription ZNF genes & repeats Strong transcription	CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
35	rs2734326	chr6:31943585-31943586	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs374248365	chr6:31943624-31943625	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs368452197	chr6:31943634-31943635	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs553695069	chr6:31943658-31943659	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs568493156	chr6:31943678-31943679	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs537923331	chr6:31943689-31943690	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs369033535	chr6:31943690-31943691	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs549527310	chr6:31943707-31943708	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs567650100	chr6:31943711-31943712	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs370657799	chr6:31943758-31943759	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs550152017	chr6:31943770-31943771	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs571806003	chr6:31943794-31943795	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs539334816	chr6:31943802-31943803	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs554044122	chr6:31943807-31943808	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs565959002	chr6:31943808-31943809	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs533624801	chr6:31943809-31943810	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:137)

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	21552322	CNVD
Immune disease	21076436	CNVD
Autoimmune disease	19135723	CNVD
Systemic lupus erythematosus	17953491	CNVD
Recurrent Infections	22737222	CNVD
Systemic lupus erythematosus	21904924	CNVD
Ovarian cancer	21781307	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
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
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
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
Cancer	22183965	CNVD
Melanoma	22183965	CNVD
Myelofibrosis	22110671	CNVD
Incontinentia Pigmenti	22033527	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Encephalopathy	20692195	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Melanoma	20877625	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD

Chromatin state (count:474 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:31940400-31941800	Flanking Active TSS	Dnd41	blood
2	chr6:31940400-31942000	Flanking Active TSS	K562	blood
3	chr6:31941000-31941800	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
4	chr6:31941000-31941800	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
5	chr6:31941000-31941800	Enhancers	Primary T helper cells fromperipheralblood	blood
6	chr6:31941000-31941800	Enhancers	Liver	Liver
7	chr6:31941000-31941800	Enhancers	Small Intestine	intestine
8	chr6:31941000-31944000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
9	chr6:31941000-31946600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
10	chr6:31941000-31946600	Weak transcription	Left Ventricle	heart
11	chr6:31941000-31946600	Weak transcription	Lung	lung
12	chr6:31941000-31947200	Weak transcription	Esophagus	oesophagus
13	chr6:31941000-31947200	Weak transcription	Ovary	ovary
14	chr6:31941000-31947200	Weak transcription	Placenta Amnion	Placenta Amnion
15	chr6:31941000-31947600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
16	chr6:31941000-31949600	Weak transcription	Right Ventricle	heart
17	chr6:31941000-31949800	Weak transcription	Gastric	stomach
18	chr6:31941200-31941800	Enhancers	Breast Myoepithelial Primary Cells	Breast
19	chr6:31941200-31941800	Enhancers	Fetal Brain Male	brain
20	chr6:31941200-31941800	Enhancers	Fetal Intestine Large	intestine
21	chr6:31941200-31942000	Weak transcription	Fetal Muscle Trunk	muscle
22	chr6:31941200-31942200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
23	chr6:31941200-31942200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
24	chr6:31941200-31942400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
25	chr6:31941200-31944400	Weak transcription	H1 Cell Line	embryonic stem cell
26	chr6:31941200-31945400	Weak transcription	Fetal Muscle Leg	muscle
27	chr6:31941200-31945800	Weak transcription	Primary T cells fromperipheralblood	blood
28	chr6:31941200-31946200	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
29	chr6:31941200-31946400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
30	chr6:31941200-31946400	Weak transcription	Placenta	Placenta
31	chr6:31941200-31946400	Weak transcription	Rectal Mucosa Donor 29	rectum
32	chr6:31941200-31946600	Weak transcription	Primary B cells from peripheral blood	blood
33	chr6:31941200-31946600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
34	chr6:31941200-31947000	Weak transcription	Pancreas	Pancrea
35	chr6:31941200-31947200	Weak transcription	HUES48 Cell Line	embryonic stem cell
36	chr6:31941200-31947200	Weak transcription	Primary neutrophils fromperipheralblood	blood
37	chr6:31941200-31947200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
38	chr6:31941200-31947200	Weak transcription	Spleen	Spleen
39	chr6:31941200-31947400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
40	chr6:31941200-31949200	Weak transcription	HUES64 Cell Line	embryonic stem cell
41	chr6:31941200-31949400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
42	chr6:31941200-31949400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
43	chr6:31941200-31950000	Weak transcription	Rectal Smooth Muscle	rectum
44	chr6:31941400-31941800	Enhancers	Primary T helper cells PMA-I stimulated	--
45	chr6:31941400-31941800	Enhancers	Muscle Satellite Cultured Cells	--
46	chr6:31941400-31941800	Enhancers	Brain Inferior Temporal Lobe	brain
47	chr6:31941400-31941800	Enhancers	HepG2	liver
48	chr6:31941400-31942000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
49	chr6:31941400-31942200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
50	chr6:31941400-31942200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain

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