Variant report

Variant	nsv970677
Chromosome Location	chr6:31020994-31026537
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:302)
CpG islands
(count:1650)
Chromatin interactive
region (count:10)
LncRNA
region (count:15)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:302 , 50 per page) page: 1 2 3 4 5 6 7

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:31026101-31026439	HepG2	liver:	n/a	n/a
2	ATF3	chr6:31025932-31026501	HCT-116	colon:	n/a	n/a
3	ATF3	chr6:31025978-31026399	K562	blood:	n/a	n/a
4	BACH1	chr6:31026186-31026404	H1-hESC	embryonic stem cell:	n/a	n/a
5	BATF	chr6:31020952-31021149	GM12878	blood:	n/a	n/a
6	BATF	chr6:31025904-31026384	GM12878	blood:	n/a	n/a
7	BHLHE40	chr6:31026151-31026353	HepG2	liver:	n/a	n/a
8	CEBPB	chr6:31025766-31026408	Hela-S3	cervix:	n/a	n/a
9	CEBPB	chr6:31025817-31026348	IMR90	lung:	n/a	n/a
10	CTCF	chr6:31026204-31026309	NHEK	skin:	n/a	n/a
11	CTCF	chr6:31026140-31026290	NHEK	skin:	n/a	n/a
12	CTCF	chr6:31026101-31026388	T-47D	breast:	n/a	n/a
13	CTCF	chr6:31026140-31026290	HRE	kidney:	n/a	n/a
14	CTCF	chr6:31026067-31026338	H1-hESC	embryonic stem cell:	n/a	n/a
15	CTCF	chr6:31026040-31026480	K562	blood:	n/a	n/a
16	CTCF	chr6:31026240-31026390	HFF-Myc	foreskin:	n/a	n/a
17	CTCF	chr6:31026180-31026330	GM12878	blood:	n/a	n/a
18	CTCF	chr6:31026180-31026330	BE2_C	brain:	n/a	n/a
19	CTCF	chr6:31026220-31026370	GM12870	blood:	n/a	n/a
20	CTCF	chr6:31026180-31026330	GM12873	blood:	n/a	n/a
21	CTCF	chr6:31026151-31026344	A549	lung:	n/a	n/a
22	CTCF	chr6:31025993-31026496	MCF-7	breast:	n/a	n/a
23	CTCF	chr6:31026220-31026370	BE2_C	brain:	n/a	n/a
24	CTCF	chr6:31026140-31026290	GM12875	blood:	n/a	n/a
25	CTCF	chr6:31026133-31026392	Hela-S3	cervix:	n/a	n/a
26	CTCF	chr6:31026180-31026330	HCT-116	colon:	n/a	n/a
27	CTCF	chr6:31026200-31026350	BJ	skin:	n/a	n/a
28	CTCF	chr6:31026160-31026310	GM12866	blood:	n/a	n/a
29	CTCF	chr6:31026220-31026370	HRE	kidney:	n/a	n/a
30	CTCF	chr6:31026180-31026330	HPF	lung:	n/a	n/a
31	CTCF	chr6:31026220-31026370	AoAF	blood vessel:	n/a	n/a
32	CTCF	chr6:31026160-31026310	HA-sp	spinal cord:	n/a	n/a
33	CTCF	chr6:31026180-31026330	NHEK	skin:	n/a	n/a
34	CTCF	chr6:31026180-31026330	GM12868	blood:	n/a	n/a
35	CTCF	chr6:31026164-31026341	Gliobla	brain:	n/a	n/a
36	CTCF	chr6:31025220-31025370	HAc	cerebellar:	n/a	n/a
37	CTCF	chr6:31026206-31026332	A549	lung:	n/a	n/a
38	CTCF	chr6:31026180-31026330	GM06990	blood:	n/a	n/a
39	CTCF	chr6:31026220-31026370	GM12864	blood:	n/a	n/a
40	CTCF	chr6:31026160-31026310	HVMF	connective:	n/a	n/a
41	CTCF	chr6:31026120-31026270	GM12873	blood:	n/a	n/a
42	CTCF	chr6:31026240-31026390	A549	lung:	n/a	n/a
43	CTCF	chr6:31026200-31026350	GM12865	blood:	n/a	n/a
44	CTCF	chr6:31026180-31026330	HCPEpiC	choroid plexus:	n/a	n/a
45	CTCF	chr6:31026200-31026350	SAEC	small airway:	n/a	n/a
46	CTCF	chr6:31026099-31026441	GM12878	blood:	n/a	n/a
47	CTCF	chr6:31026110-31026436	HUVEC	blood vessel:	n/a	n/a
48	CTCF	chr6:31026180-31026330	GM12801	blood:	n/a	n/a
49	CTCF	chr6:31026220-31026370	AG04450	lung:	n/a	n/a
50	CTCF	chr6:31026180-31026330	HUVEC	blood vessel:	n/a	n/a

(count:1650 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:31023763-31023813	MCF10A-Er-Src	breast:	n/a
2	chr6:31023286-31023336	AG09319	gingival:	n/a
3	chr6:31026215-31026265	IMR90	lung:	fetal
4	chr6:31023763-31023813	MCF10A-Er-Src	breast:	n/a
5	chr6:31023286-31023336	AG09319	gingival:	n/a
6	chr6:31026215-31026265	IMR90	lung:	fetal
7	chr6:31021957-31022007	BJ	skin:	n/a
8	chr6:31021744-31021794	PrEC	prostate:	n/a
9	chr6:31023763-31023813	HEEpiC	esophagus:	n/a
10	chr6:31021275-31021325	SAEC	small airway:	n/a
11	chr6:31025933-31025983	SK-N-SH_RA	brain:	n/a
12	chr6:31021796-31021846	GM19239	blood:	n/a
13	chr6:31026287-31026337	CMK	blood:	n/a
14	chr6:31024501-31024551	NT2-D1	testis:	n/a
15	chr6:31022286-31022336	AoSMC	blood vessel:	n/a
16	chr6:31024990-31025040	SK-N-SH_RA	brain:	n/a
17	chr6:31023763-31023813	AG04449	skin:	fetal
18	chr6:31025014-31025064	AG09309	skin:	n/a
19	chr6:31021826-31021876	NB4	blood:	n/a
20	chr6:31026105-31026155	T-47D	breast:	n/a
21	chr6:31024191-31024241	SK-N-SH_RA	brain:	n/a
22	chr6:31021134-31021184	HAEpiC	amniotic membrane:	n/a
23	chr6:31021422-31021472	H1-hESC	embryonic stem cell:	embryo
24	chr6:31023286-31023336	SK-N-SH	brain:	n/a
25	chr6:31023257-31023307	HRE	kidney:	n/a
26	chr6:31021275-31021325	HepG2	liver:	n/a
27	chr6:31025933-31025983	HEK293	kidney:	embryo
28	chr6:31022286-31022336	SK-N-MC	brain:	n/a
29	chr6:31023592-31023642	CMK	blood:	n/a
30	chr6:31021275-31021325	HCT-116	colon:	n/a
31	chr6:31023257-31023307	HPAEpiC	pulmonary alveolar:	n/a
32	chr6:31025967-31026017	NHDF-neo	bronchial:	n/a
33	chr6:31021957-31022007	Jurkat	blood:	n/a
34	chr6:31023286-31023336	T-47D	breast:	n/a
35	chr6:31023592-31023642	HCT-116	colon:	n/a
36	chr6:31022598-31022648	HepG2	liver:	n/a
37	chr6:31024501-31024551	HepG2	liver:	n/a
38	chr6:31024501-31024551	HEEpiC	esophagus:	n/a
39	chr6:31023709-31023759	MCF10A-Er-Src	breast:	n/a
40	chr6:31021275-31021325	Hela-S3	cervix:	n/a
41	chr6:31021365-31021415	PFSK-1	brain:	n/a
42	chr6:31021744-31021794	BJ	skin:	n/a
43	chr6:31026105-31026155	HRCEpiC	kidney:	n/a
44	chr6:31025949-31025999	HCF	heart:	n/a
45	chr6:31025933-31025983	PFSK-1	brain:	n/a
46	chr6:31026215-31026265	Caco-2	colon:	n/a
47	chr6:31023286-31023336	HUVEC	blood vessel:	n/a
48	chr6:31025933-31025983	BJ	skin:	n/a
49	chr6:31021744-31021794	HUVEC	blood vessel:	n/a
50	chr6:31023770-31023820	Caco-2	colon:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr6:30710166..30712547-chr6:31022395..31024749,2	MCF-7	breast:
2	chr6:31025998..31026666-chr6:31047275..31048136,2	K562	blood:
3	chr6:31018538..31021131-chr6:31024335..31025981,2	K562	blood:
4	chr6:30852059..30854208-chr6:31023741..31026311,2	MCF-7	breast:
5	chr6:31010860..31013816-chr6:31025922..31027807,2	K562	blood:
6	chr6:31018538..31021131-chr6:31024335..31025981,2	K562	blood:
7	chr6:31026121..31026747-chr6:31038216..31039119,3	MCF-7	breast:
8	chr6:30883366..30884420-chr6:31026193..31027023,3	MCF-7	breast:
9	chr6:30920933..30923487-chr6:31026519..31028176,2	K562	blood:
10	chr6:31025808..31026599-chr6:31047303..31047806,2	MCF-7	breast:

(count:15 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-MUC22-1	chr6:31023589-31023778	ENSG00000228789.2
2	lnc-MUC22-1	chr6:31021984-31027653	XLOC_005243
3	lnc-MUC22-1	chr6:31023487-31024687	ENSG00000228789
4	lnc-MUC22-1	chr6:31021984-31022293	ENSG00000228789
5	lnc-MUC22-1	chr6:31021979-31022293	ENSG00000228789.2
6	lnc-MUC22-1	chr6:31021984-31022282	ENSG00000228789.2
7	lnc-MUC22-1	chr6:31021262-31021308	NONHSAT108711
8	lnc-MUC22-1	chr6:31023487-31024251	ENSG00000228789.2
9	lnc-MUC22-1	chr6:31021277-31021308	ENSG00000228789.2
10	lnc-MUC22-1	chr6:31021877-31022293	ENSG00000228789.2
11	lnc-MUC22-1	chr6:31021227-31021308	NONHSAT108710
12	lnc-MUC22-1	chr6:31021227-31021308	ENSG00000228789.2
13	lnc-MUC22-1	chr6:31021877-31022293	NONHSAT108710
14	lnc-MUC22-1	chr6:31023487-31024687	NONHSAT108710
15	lnc-MUC22-1	chr6:31023995-31024687	ENSG00000228789.2

No data

Variant related genes	Relation type
HCG22	TF binding region
HCG22	CpG island
ENSG00000137331	chromatin interactions
ENSG00000272273	chromatin interactions
ENSG00000204580	chromatin interactions
ENSG00000137411	chromatin interactions
ENSG00000137312	chromatin interactions
ENSG00000233529	chromatin interactions

Extended variants
information (count: 232 )
Associated
traits (count: 120 )

Variant overlapped rSNPs/rCNVs (count:232 , 50 per page) page: 1 2 3 4 5

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs559598934	chr6:31021009-31021010	Weak transcription Enhancers ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs4713429	chr6:31021017-31021018	Weak transcription Enhancers ZNF genes & repeats	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
3	rs548395150	chr6:31021030-31021031	Weak transcription Enhancers ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs531092627	chr6:31021110-31021111	Weak transcription Enhancers ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs552499532	chr6:31021156-31021157	Weak transcription Enhancers ZNF genes & repeats	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
6	rs9262615	chr6:31021161-31021162	Weak transcription Enhancers ZNF genes & repeats	TF binding region CpG island	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
7	rs113489016	chr6:31021266-31021267	Weak transcription Enhancers Bivalent Enhancer ZNF genes & repeats	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
8	rs572644321	chr6:31021274-31021275	Weak transcription Enhancers Bivalent Enhancer ZNF genes & repeats	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
9	rs553784319	chr6:31021275-31021276	Weak transcription Enhancers Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island lncRNA	1 gene(s)	Overlapped CNVs	n/a
10	rs565662144	chr6:31021276-31021277	Weak transcription Enhancers Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island lncRNA	1 gene(s)	Overlapped CNVs	n/a
11	rs2428516	chr6:31021325-31021326	Weak transcription Enhancers Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
12	rs561402321	chr6:31021416-31021417	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs528906826	chr6:31021428-31021429	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
14	rs2523857	chr6:31021504-31021505	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer ZNF genes & repeats	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
15	rs142899109	chr6:31021527-31021528	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
16	rs117803081	chr6:31021542-31021543	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
17	rs180734937	chr6:31021546-31021547	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
18	rs2517527	chr6:31021547-31021548	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
19	rs541068945	chr6:31021559-31021560	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
20	rs376583522	chr6:31021574-31021575	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
21	rs559769480	chr6:31021576-31021577	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
22	rs2523856	chr6:31021630-31021631	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
23	rs541953313	chr6:31021656-31021657	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs147747618	chr6:31021659-31021660	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs566660794	chr6:31021697-31021698	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs531051679	chr6:31021718-31021719	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs552413020	chr6:31021728-31021729	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs571061632	chr6:31021745-31021746	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
29	rs532106972	chr6:31021773-31021774	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
30	rs545069670	chr6:31021783-31021784	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
31	rs565705576	chr6:31021790-31021791	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
32	rs142664255	chr6:31021831-31021832	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
33	rs184777175	chr6:31021839-31021840	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
34	rs537250344	chr6:31021863-31021864	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
35	rs146228541	chr6:31021873-31021874	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
36	rs558767585	chr6:31021886-31021887	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
37	rs577084597	chr6:31021901-31021902	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
38	rs532863594	chr6:31021913-31021914	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
39	rs553074849	chr6:31021935-31021936	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
40	rs117264051	chr6:31021957-31021958	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats	TF binding region CpG island lncRNA	1 gene(s)	Overlapped CNVs	n/a
41	rs147109000	chr6:31021996-31021997	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats	lncRNA	n/a	Overlapped CNVs	n/a
42	rs371277367	chr6:31022040-31022041	Enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS Active TSS Bivalent Enhancer ZNF genes & repeats	lncRNA	n/a	Overlapped CNVs	n/a
43	rs528690898	chr6:31022061-31022062	Enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS Active TSS Bivalent Enhancer ZNF genes & repeats	lncRNA	n/a	Overlapped CNVs	n/a
44	rs147569343	chr6:31022100-31022101	Enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS Active TSS Bivalent Enhancer ZNF genes & repeats	lncRNA	n/a	Overlapped CNVs	n/a
45	rs3873352	chr6:31022113-31022114	Enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS Active TSS Bivalent Enhancer ZNF genes & repeats	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
46	rs2523855	chr6:31022158-31022159	Enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS Active TSS Bivalent Enhancer ZNF genes & repeats	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
47	rs564769502	chr6:31022161-31022162	Enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS Active TSS Bivalent Enhancer ZNF genes & repeats	lncRNA	n/a	Overlapped CNVs	n/a
48	rs141943201	chr6:31022196-31022197	Enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS Active TSS Bivalent Enhancer ZNF genes & repeats	lncRNA	n/a	Overlapped CNVs	n/a
49	rs189139528	chr6:31022228-31022229	Weak transcription Enhancers Active TSS ZNF genes & repeats	lncRNA	n/a	Overlapped CNVs	n/a
50	rs3915966	chr6:31022274-31022275	Weak transcription Enhancers Active TSS ZNF genes & repeats	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:120)

Disease	PMID	Source
Acute lymphoblastic leukemia	22237106	CNVD
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	22844521	CNVD
HIV/AIDS	22844521	CNVD
Ovarian cancer	22844521	CNVD
Prostate cancer	22844521	CNVD
Psoriasis	22844521	CNVD
Rheumatoid arthritis	22844521	CNVD
Sclerosis systemic	22844521	CNVD
Systemic lupus erythematosus	22844521	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
Gestational infection	22844521	CNVD
Head circumference	22844521	CNVD
Infertility	22844521	CNVD
Recurrent birth weight diabetes	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
Hodgkin''s lymphoma	18641027	CNVD
lymphocytic leukemia	21291569	CNVD

Chromatin state (count:136 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:31009600-31027400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr6:31010600-31021600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr6:31013800-31021600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
4	chr6:31016200-31021600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr6:31020800-31021400	Enhancers	Primary B cells from peripheral blood	blood
6	chr6:31020800-31021400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
7	chr6:31020800-31021600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
8	chr6:31020800-31022200	Enhancers	Fetal Heart	heart
9	chr6:31020800-31022400	Enhancers	Cortex derived primary cultured neurospheres	brain
10	chr6:31020800-31022400	ZNF genes & repeats	GM12878-XiMat	blood
11	chr6:31021200-31021600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
12	chr6:31021200-31021600	Enhancers	Brain Germinal Matrix	brain
13	chr6:31021200-31022000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
14	chr6:31021200-31022200	Bivalent Enhancer	Fetal Stomach	stomach
15	chr6:31021400-31021600	Enhancers	Fetal Kidney	kidney
16	chr6:31021400-31022000	Enhancers	Fetal Brain Male	brain
17	chr6:31021400-31022200	Enhancers	Primary hematopoietic stem cells	blood
18	chr6:31021400-31022200	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
19	chr6:31021600-31021800	Bivalent Enhancer	H9 Derived Neuron Cultured Cells	ES cell derived
20	chr6:31021600-31021800	Bivalent Enhancer	IMR90 fetal lung fibroblasts Cell Line	lung
21	chr6:31021600-31021800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
22	chr6:31021600-31021800	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
23	chr6:31021600-31021800	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin03	Skin
24	chr6:31021600-31021800	Enhancers	Fetal Lung	lung
25	chr6:31021600-31021800	Bivalent/Poised TSS	Fetal Muscle Leg	muscle
26	chr6:31021600-31021800	Bivalent Enhancer	Fetal Thymus	thymus
27	chr6:31021600-31022000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
28	chr6:31021600-31022000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
29	chr6:31021600-31022000	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin
30	chr6:31021600-31022000	Flanking Active TSS	Brain Germinal Matrix	brain
31	chr6:31021600-31022000	Flanking Bivalent TSS/Enh	Fetal Muscle Trunk	muscle
32	chr6:31021600-31022200	Enhancers	H1 Cell Line	embryonic stem cell
33	chr6:31021600-31022200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
34	chr6:31021600-31022200	Enhancers	HUES64 Cell Line	embryonic stem cell
35	chr6:31021600-31022200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
36	chr6:31021600-31022200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
37	chr6:31021600-31022400	Active TSS	Brain Anterior Caudate	brain
38	chr6:31021800-31022000	Flanking Bivalent TSS/Enh	Foreskin Fibroblast Primary Cells skin02	Skin
39	chr6:31021800-31022000	Bivalent Enhancer	Primary mononuclear cells fromperipheralblood	Blood
40	chr6:31021800-31022200	Enhancers	Primary hematopoietic stem cells short term culture	blood
41	chr6:31021800-31022200	Bivalent Enhancer	Fetal Muscle Leg	muscle
42	chr6:31022000-31022200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
43	chr6:31022000-31022200	Bivalent/Poised TSS	Foreskin Fibroblast Primary Cells skin01	Skin
44	chr6:31022000-31022200	Enhancers	Brain Germinal Matrix	brain
45	chr6:31022000-31022200	Bivalent Enhancer	Fetal Muscle Trunk	muscle
46	chr6:31022000-31022600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
47	chr6:31022000-31023800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
48	chr6:31022200-31022400	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
49	chr6:31022200-31024600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
50	chr6:31022200-31024800	Weak transcription	Brain Germinal Matrix	brain

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