Variant report

Variant	nsv884524
Chromosome Location	chr6:31947359-32003881
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:683)
CpG islands
(count:2259)
Chromatin interactive
region (count:5)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:2)

(count:683 , 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	chr6:31947365-31947781	K562	blood:	n/a	n/a
2	BHLHE40	chr6:31970701-31971047	HepG2	liver:	n/a	n/a
3	BHLHE40	chr6:31947116-31947502	K562	blood:	n/a	n/a
4	BHLHE40	chr6:31982297-31982618	HepG2	liver:	n/a	n/a
5	BHLHE40	chr6:31949559-31949880	HepG2	liver:	n/a	n/a
6	BHLHE40	chr6:32003438-32003784	HepG2	liver:	n/a	n/a
7	CBX3	chr6:31980155-31981063	K562	blood:	n/a	n/a
8	CBX3	chr6:31946996-31947474	K562	blood:	n/a	n/a
9	CBX3	chr6:31965417-31965721	K562	blood:	n/a	n/a
10	CBX3	chr6:31990799-31991208	K562	blood:	n/a	n/a
11	CBX3	chr6:31957963-31958493	K562	blood:	n/a	n/a
12	CBX3	chr6:32003260-32004138	K562	blood:	n/a	n/a
13	CBX3	chr6:31970603-31971015	K562	blood:	n/a	n/a
14	CBX3	chr6:32003387-32003757	K562	blood:	n/a	n/a
15	CBX3	chr6:31982302-31982628	K562	blood:	n/a	n/a
16	CBX3	chr6:31958022-31958441	K562	blood:	n/a	n/a
17	CBX3	chr6:31985480-31985931	K562	blood:	n/a	n/a
18	CBX3	chr6:31985535-31985921	K562	blood:	n/a	n/a
19	CBX3	chr6:31990712-31991199	K562	blood:	n/a	n/a
20	CBX3	chr6:31989858-31990273	K562	blood:	n/a	n/a
21	CBX3	chr6:31970387-31971162	K562	blood:	n/a	n/a
22	CBX3	chr6:31989920-31990157	K562	blood:	n/a	n/a
23	CBX3	chr6:31952664-31953239	K562	blood:	n/a	n/a
24	CBX3	chr6:31952793-31953135	K562	blood:	n/a	n/a
25	CCNT2	chr6:31947256-31947610	K562	blood:	n/a	n/a
26	CEBPB	chr6:32003276-32004129	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	CEBPD	chr6:31970600-31971236	K562	blood:	n/a	n/a
31	CEBPD	chr6:31980664-31980987	K562	blood:	n/a	n/a
32	CEBPD	chr6:31972233-31972447	HepG2	liver:	n/a	n/a
33	CEBPD	chr6:32003343-32003982	K562	blood:	n/a	n/a
34	CHD2	chr6:31947206-31947389	K562	blood:	n/a	n/a
35	CTCF	chr6:31947360-31947510	GM12873	blood:	n/a	n/a
36	CTCF	chr6:31957624-31957654	MCF-7	breast:	n/a	n/a
37	CTCF	chr6:31973425-31973542	H1-hESC	embryonic stem cell:	n/a	n/a
38	CTCF	chr6:31990379-31990406	GM12892	blood:	n/a	n/a
39	CTCF	chr6:31989985-31990211	K562	blood:	n/a	n/a
40	CTCF	chr6:31964104-31964114	MCF-7	breast:	n/a	n/a
41	CTCF	chr6:31984864-31984882	GM10266	blood:	n/a	n/a
42	CTCF	chr6:31957606-31957675	GM12892	blood:	n/a	n/a
43	CTCF	chr6:31973422-31973567	MCF-7	breast:	n/a	n/a
44	CTCF	chr6:31957163-31957472	K562	blood:	n/a	n/a
45	CTCF	chr6:31989973-31990183	MCF-7	breast:	n/a	n/a
46	CTCF	chr6:31950381-31950434	LNCaP	prostate:	n/a	n/a
47	CTCF	chr6:31950070-31950231	GM19238	blood:	n/a	n/a
48	CTCF	chr6:31971107-31971165	GM10266	blood:	n/a	n/a
49	CTCF	chr6:31975032-31975152	HepG2	liver:	n/a	n/a
50	CTCF	chr6:31957268-31957413	MCF-7	breast:	n/a	n/a

(count:2259 , 50 per page) page: 1 2 3 4 5 6 7 ... 46

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:31964754-31964804	Hepatocyte	liver:	n/a
2	chr6:31973255-31973305	AG09319	gingival:	n/a
3	chr6:31964754-31964804	Hepatocyte	liver:	n/a
4	chr6:31973255-31973305	AG09319	gingival:	n/a
5	chr6:31963526-31963576	NT2-D1	testis:	n/a
6	chr6:31977443-31977493	NHBE	bronchial:	n/a
7	chr6:31964274-31964324	HCPEpiC	choroid plexus:	n/a
8	chr6:31977443-31977493	HIPEpiC	eye:	n/a
9	chr6:31973345-31973395	HRCEpiC	kidney:	n/a
10	chr6:31980043-31980093	HNPCEpiC	eye:	n/a
11	chr6:31973180-31973230	ovcar-3	ovarian:	n/a
12	chr6:31973051-31973101	ProgFib	skin:	n/a
13	chr6:31963912-31963962	AoSMC	blood vessel:	n/a
14	chr6:31980856-31980906	RPTEC	kidney:	n/a
15	chr6:31996931-31996981	HCPEpiC	choroid plexus:	n/a
16	chr6:31963919-31963969	NT2-D1	testis:	n/a
17	chr6:31973162-31973212	Jurkat	blood:	n/a
18	chr6:31963526-31963576	RPTEC	kidney:	n/a
19	chr6:31973180-31973230	SK-N-SH	brain:	n/a
20	chr6:31963526-31963576	HEEpiC	esophagus:	n/a
21	chr6:31980046-31980096	ProgFib	skin:	n/a
22	chr6:31997059-31997109	HCF	heart:	n/a
23	chr6:31964193-31964243	Hela-S3	cervix:	n/a
24	chr6:31978789-31978839	SKMC	muscle:	n/a
25	chr6:31996931-31996981	GM12891	blood:	n/a
26	chr6:31997059-31997109	Caco-2	colon:	n/a
27	chr6:31980856-31980906	GM06990	blood:	n/a
28	chr6:31976687-31976737	BE2_C	brain:	n/a
29	chr6:31980043-31980093	HIPEpiC	eye:	n/a
30	chr6:31973345-31973395	LNCaP	prostate:	n/a
31	chr6:31976687-31976737	HEK293	kidney:	embryo
32	chr6:31996657-31996707	HCT-116	colon:	n/a
33	chr6:31964754-31964804	SKMC	muscle:	n/a
34	chr6:31973051-31973101	SAEC	small airway:	n/a
35	chr6:31997491-31997541	ECC-1	luminal epithelium:	n/a
36	chr6:31973051-31973101	NHBE	bronchial:	n/a
37	chr6:31973051-31973101	HRPEpiC	eye:	n/a
38	chr6:31964274-31964324	PANC-1	pancreas:	n/a
39	chr6:31978789-31978839	A549	lung:	n/a
40	chr6:31980845-31980895	AG09319	gingival:	n/a
41	chr6:31996931-31996981	Hela-S3	cervix:	n/a
42	chr6:31963912-31963962	HEEpiC	esophagus:	n/a
43	chr6:31978789-31978839	NHBE	bronchial:	n/a
44	chr6:31976548-31976598	MCF10A-Er-Src	breast:	n/a
45	chr6:31973255-31973305	U87	brain:	n/a
46	chr6:31997059-31997109	U87	brain:	n/a
47	chr6:31963912-31963962	HCT-116	colon:	n/a
48	chr6:31997026-31997076	HCPEpiC	choroid plexus:	n/a
49	chr6:31980052-31980102	T-47D	breast:	n/a
50	chr6:31974906-31974956	HRE	kidney:	n/a

(count:5 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:31868623..31870778-chr6:31945874..31948322,2	K562	blood:
2	chr6:31935647..31937211-chr6:31946410..31948036,2	K562	blood:
3	chr6:31912743..31916758-chr6:31944927..31949257,3	K562	blood:
4	chr6:31938987..31942159-chr6:31944563..31949146,6	MCF-7	breast:
5	chr6:31937794..31943427-chr6:31944150..31949640,18	K562	blood:

(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-DOM3Z-2	chr6:31970797-31971298	ENSG00000233627.2
3	lnc-TNXB-6	chr6:32003534-32004035	ENSG00000229776.1
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
CYP21A2	TF binding region
STK19	TF binding region
CYP21A1P	TF binding region
ENSG00000268923	TF binding region
C4A-AS1	TF binding region
C4A	TF binding region
C4B	TF binding region
TNXA	CpG island
STK19P	CpG island
CYP21A2	CpG island
STK19	CpG island
CYP21A1P	CpG island
ENSG00000268923	CpG island
C4A-AS1	CpG island
C4A	CpG island
C4B	CpG island
ENSG00000204348	chromatin interactions
ENSG00000204351	chromatin interactions
ENSG00000204366	chromatin interactions
ENSG00000204344	chromatin interactions
ENSG00000243649	chromatin interactions
ENSG00000166278	chromatin interactions

Extended variants
information (count: 691 )
Associated
traits (count: 137 )

Variant overlapped rSNPs/rCNVs (count:691 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs56291783	chr6:31947359-31947360	Strong transcription Weak transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
2	rs535571273	chr6:31947367-31947368	Strong transcription Weak transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
3	rs547172921	chr6:31947410-31947411	Strong transcription Weak transcription Enhancers Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
4	rs557301089	chr6:31947447-31947448	Strong transcription Weak transcription Enhancers Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
5	rs575582378	chr6:31947457-31947458	Strong transcription Weak transcription Enhancers Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
6	rs389883	chr6:31947460-31947461	Strong transcription Weak transcription Enhancers Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	8 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
7	rs389512	chr6:31947594-31947595	Strong transcription Weak transcription Enhancers Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	8 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
8	rs551245949	chr6:31947634-31947635	Strong transcription Weak transcription Enhancers Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
9	rs573578869	chr6:31947652-31947653	Strong transcription Weak transcription Enhancers Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
10	rs368999420	chr6:31947683-31947684	Strong transcription Weak transcription Enhancers Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
11	rs147233808	chr6:31947692-31947693	Strong transcription Weak transcription Enhancers Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
12	rs562280820	chr6:31947706-31947707	Strong transcription Weak transcription Enhancers Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
13	rs574554664	chr6:31947748-31947749	Strong transcription Weak transcription Enhancers Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
14	rs116196017	chr6:31947804-31947805	Strong transcription Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
15	rs377573133	chr6:31947890-31947891	Strong transcription Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
16	rs533783241	chr6:31947901-31947902	Strong transcription Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
17	rs114632474	chr6:31947917-31947918	Strong transcription Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
18	rs551482064	chr6:31948006-31948007	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
19	rs530467043	chr6:31948016-31948017	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
20	rs118178906	chr6:31948022-31948023	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
21	rs6904886	chr6:31948029-31948030	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
22	rs563992443	chr6:31948060-31948061	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
23	rs140857097	chr6:31948091-31948092	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
24	rs9391732	chr6:31948097-31948098	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
25	rs190486403	chr6:31948107-31948108	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
26	rs533747654	chr6:31948131-31948132	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
27	rs182148351	chr6:31948155-31948156	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
28	rs569231522	chr6:31948201-31948202	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
29	rs376107079	chr6:31948202-31948203	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
30	rs558139309	chr6:31948217-31948218	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
31	rs369081587	chr6:31948226-31948227	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
32	rs573540461	chr6:31948255-31948256	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
33	rs373414495	chr6:31948256-31948257	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
34	rs534517982	chr6:31948260-31948261	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
35	rs151183324	chr6:31948272-31948273	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
36	rs140503088	chr6:31948275-31948276	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
37	rs267600972	chr6:31948278-31948279	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
38	rs200696149	chr6:31948311-31948312	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
39	rs28441225	chr6:31948400-31948401	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs200620398	chr6:31948422-31948423	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs70990293	chr6:31948425-31948426	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs201442394	chr6:31948433-31948434	Weak transcription Strong transcription Genic enhancers	CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
43	rs371041447	chr6:31948452-31948453	Weak transcription Strong transcription Genic enhancers	CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
44	rs142791776	chr6:31948473-31948474	Weak transcription Strong transcription Genic enhancers	CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
45	rs41267122	chr6:31948474-31948475	Weak transcription Strong transcription Genic enhancers	CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
46	rs201134143	chr6:31948502-31948503	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs561534965	chr6:31948507-31948508	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs529123063	chr6:31948524-31948525	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs550753928	chr6:31948533-31948534	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs569210209	chr6:31948542-31948543	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 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:269 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:31941000-31947600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
2	chr6:31941000-31949600	Weak transcription	Right Ventricle	heart
3	chr6:31941000-31949800	Weak transcription	Gastric	stomach
4	chr6:31941200-31947400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
5	chr6:31941200-31949200	Weak transcription	HUES64 Cell Line	embryonic stem cell
6	chr6:31941200-31949400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
7	chr6:31941200-31949400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
8	chr6:31941200-31950000	Weak transcription	Rectal Smooth Muscle	rectum
9	chr6:31941400-31947400	Weak transcription	Rectal Mucosa Donor 31	rectum
10	chr6:31941400-31947600	Weak transcription	Sigmoid Colon	Sigmoid Colon
11	chr6:31941400-31949000	Weak transcription	Colonic Mucosa	Colon
12	chr6:31941400-31949400	Weak transcription	Primary B cells from cord blood	blood
13	chr6:31941400-31949400	Weak transcription	NH-A	brain
14	chr6:31941400-31950000	Weak transcription	Fetal Kidney	kidney
15	chr6:31941600-31947600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
16	chr6:31941600-31947600	Weak transcription	Brain Cingulate Gyrus	brain
17	chr6:31941600-31947800	Weak transcription	Fetal Lung	lung
18	chr6:31941600-31948000	Weak transcription	Hela-S3	cervix
19	chr6:31941600-31949200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
20	chr6:31941600-31949200	Weak transcription	Colon Smooth Muscle	Colon
21	chr6:31941600-31950000	Weak transcription	Skeletal Muscle Female	skeletal muscle
22	chr6:31941800-31948600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
23	chr6:31941800-31950000	Weak transcription	Dnd41	blood
24	chr6:31943200-31947400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
25	chr6:31944800-31948400	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
26	chr6:31945400-31948400	Strong transcription	Fetal Muscle Leg	muscle
27	chr6:31945800-31947400	Enhancers	Primary T helper cells fromperipheralblood	blood
28	chr6:31945800-31947800	Enhancers	Primary T cells from cord blood	blood
29	chr6:31945800-31947800	Enhancers	Primary T helper naive cells fromperipheralblood	blood
30	chr6:31945800-31948400	Strong transcription	Breast Myoepithelial Primary Cells	Breast
31	chr6:31945800-31948400	Strong transcription	Fetal Brain Female	brain
32	chr6:31946000-31947400	Enhancers	Primary T killer naive cells fromperipheralblood	blood
33	chr6:31946000-31947800	Enhancers	Primary T helper naive cells from peripheral blood	blood
34	chr6:31946000-31947800	Enhancers	Primary T helper cells PMA-I stimulated	--
35	chr6:31946000-31948200	Enhancers	Primary T killer memory cells from peripheral blood	blood
36	chr6:31946000-31948200	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
37	chr6:31946200-31947400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
38	chr6:31946400-31948200	Strong transcription	Placenta	Placenta
39	chr6:31946400-31948400	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
40	chr6:31946400-31948400	Strong transcription	Brain Germinal Matrix	brain
41	chr6:31946400-31948400	Strong transcription	Brain Hippocampus Middle	brain
42	chr6:31946400-31948400	Strong transcription	Duodenum Smooth Muscle	Duodenum
43	chr6:31946400-31948400	Strong transcription	Rectal Mucosa Donor 29	rectum
44	chr6:31946600-31947400	Genic enhancers	Primary hematopoietic stem cells short term culture	blood
45	chr6:31946600-31947400	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
46	chr6:31946600-31947800	Strong transcription	Foreskin Fibroblast Primary Cells skin02	Skin
47	chr6:31946600-31948200	Strong transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
48	chr6:31946600-31948200	Strong transcription	Cortex derived primary cultured neurospheres	brain
49	chr6:31946600-31948400	Strong transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
50	chr6:31946600-31948400	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived

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