Variant report

Variant	esv3391943
Chromosome Location	chr16:30758851-30761899
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:535)
CpG islands
(count:733)
Chromatin interactive
region (count:23)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:535 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr16:30759462-30759790	HepG2	liver:	n/a	n/a
2	ATF1	chr16:30759381-30759784	K562	blood:	n/a	n/a
3	ATF2	chr16:30758876-30759618	GM12878	blood:	n/a	n/a
4	ATF3	chr16:30759346-30759534	GM12878	blood:	n/a	n/a
5	ATF3	chr16:30759286-30759643	HepG2	liver:	n/a	n/a
6	ATF3	chr16:30759232-30759711	H1-hESC	embryonic stem cell:	n/a	n/a
7	ATF3	chr16:30759256-30759656	GM12878	blood:	n/a	n/a
8	ATF3	chr16:30759328-30759844	K562	blood:	n/a	n/a
9	ATF3	chr16:30759342-30759559	H1-hESC	embryonic stem cell:	n/a	n/a
10	BACH1	chr16:30758819-30759059	K562	blood:	n/a	n/a
11	BCL3	chr16:30758733-30759881	A549	lung:	n/a	n/a
12	BCL3	chr16:30759163-30759978	A549	lung:	n/a	n/a
13	BCL3	chr16:30759243-30759884	GM12878	blood:	n/a	n/a
14	BCLAF1	chr16:30759104-30759607	GM12878	blood:	n/a	n/a
15	BHLHE40	chr16:30759153-30759765	GM12878	blood:	n/a	n/a
16	BHLHE40	chr16:30759066-30759818	K562	blood:	n/a	n/a
17	BHLHE40	chr16:30759224-30759894	HepG2	liver:	n/a	n/a
18	BHLHE40	chr16:30759230-30759628	HepG2	liver:	n/a	n/a
19	BHLHE40	chr16:30758984-30759627	A549	lung:	n/a	n/a
20	BRCA1	chr16:30759750-30759806	HepG2	liver:	n/a	n/a
21	BRCA1	chr16:30759409-30759778	Hela-S3	cervix:	n/a	n/a
22	CBX3	chr16:30759062-30759714	K562	blood:	n/a	n/a
23	CCNT2	chr16:30759369-30759810	K562	blood:	n/a	n/a
24	CEBPB	chr16:30759392-30759699	Hela-S3	cervix:	n/a	n/a
25	CEBPB	chr16:30759576-30759588	K562	blood:	n/a	n/a
26	CEBPD	chr16:30759237-30759953	HepG2	liver:	n/a	n/a
27	CHD1	chr16:30759715-30759883	GM12878	blood:	n/a	n/a
28	CHD2	chr16:30759474-30759749	HepG2	liver:	n/a	n/a
29	CHD2	chr16:30759380-30759820	H1-hESC	embryonic stem cell:	n/a	n/a
30	CHD2	chr16:30759397-30759817	GM12878	blood:	n/a	n/a
31	CHD2	chr16:30759321-30759898	Hela-S3	cervix:	n/a	n/a
32	CHD2	chr16:30759494-30759702	K562	blood:	n/a	n/a
33	CREB1	chr16:30759295-30759709	A549	lung:	n/a	n/a
34	CREB1	chr16:30759990-30760355	H1-hESC	embryonic stem cell:	n/a	n/a
35	CREB1	chr16:30760028-30760269	A549	lung:	n/a	n/a
36	CREB1	chr16:30759340-30760362	H1-hESC	embryonic stem cell:	n/a	n/a
37	CREB1	chr16:30759095-30759960	GM12878	blood:	n/a	n/a
38	CREB1	chr16:30759243-30759975	H1-hESC	embryonic stem cell:	n/a	n/a
39	CREB1	chr16:30759303-30760367	K562	blood:	n/a	n/a
40	CREB1	chr16:30758811-30759996	HepG2	liver:	n/a	n/a
41	CREB1	chr16:30759171-30759950	A549	lung:	n/a	n/a
42	CTCF	chr16:30759740-30759890	HepG2	liver:	n/a	n/a
43	CTCF	chr16:30759440-30759590	AG04449	skin:	n/a	chr16:30759505-30759521 chr16:30759499-30759520 chr16:30759506-30759519 chr16:30759504-30759522
44	CTCF	chr16:30759260-30759410	NHLF	lung:	n/a	n/a
45	CTCF	chr16:30760474-30760516	Fibrobl	skin:	n/a	n/a
46	CTCF	chr16:30759660-30759810	AG04449	skin:	n/a	n/a
47	CTCF	chr16:30759453-30759588	Lung_OC	lung:	n/a	chr16:30759505-30759521 chr16:30759499-30759520 chr16:30759506-30759519 chr16:30759504-30759522
48	CTCF	chr16:30759600-30759750	GM12865	blood:	n/a	n/a
49	CTCF	chr16:30759280-30759430	HEEpiC	esophagus:	n/a	n/a
50	CTCF	chr16:30759422-30759679	Spleen_OC	spleen:	n/a	chr16:30759505-30759521 chr16:30759499-30759520 chr16:30759506-30759519 chr16:30759504-30759522

(count:733 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr16:30759178-30759228	PrEC	prostate:	n/a
2	chr16:30759178-30759228	PrEC	prostate:	n/a
3	chr16:30760815-30760865	SK-N-SH_RA	brain:	n/a
4	chr16:30759507-30759557	HRCEpiC	kidney:	n/a
5	chr16:30759507-30759557	K562	blood:	n/a
6	chr16:30760186-30760236	HepG2	liver:	n/a
7	chr16:30759608-30759658	Caco-2	colon:	n/a
8	chr16:30760815-30760865	SKMC	muscle:	n/a
9	chr16:30758831-30758881	HCPEpiC	choroid plexus:	n/a
10	chr16:30759703-30759753	HPAEpiC	pulmonary alveolar:	n/a
11	chr16:30758831-30758881	BJ	skin:	n/a
12	chr16:30759675-30759725	PANC-1	pancreas:	n/a
13	chr16:30759608-30759658	HRPEpiC	eye:	n/a
14	chr16:30759441-30759491	AG09319	gingival:	n/a
15	chr16:30759441-30759491	AG04449	skin:	fetal
16	chr16:30759507-30759557	HepG2	liver:	n/a
17	chr16:30760244-30760294	AG09309	skin:	n/a
18	chr16:30759703-30759753	Jurkat	blood:	n/a
19	chr16:30759703-30759753	AG09309	skin:	n/a
20	chr16:30758831-30758881	HCT-116	colon:	n/a
21	chr16:30760244-30760294	HRPEpiC	eye:	n/a
22	chr16:30759675-30759725	NH-A	brain:	n/a
23	chr16:30759441-30759491	SK-N-SH	brain:	n/a
24	chr16:30759310-30759360	CMK	blood:	n/a
25	chr16:30759703-30759753	ProgFib	skin:	n/a
26	chr16:30760244-30760294	HRE	kidney:	n/a
27	chr16:30760244-30760294	GM12892	blood:	n/a
28	chr16:30759703-30759753	Hela-S3	cervix:	n/a
29	chr16:30759675-30759725	SK-N-SH_RA	brain:	n/a
30	chr16:30760815-30760865	PANC-1	pancreas:	n/a
31	chr16:30759178-30759228	Jurkat	blood:	n/a
32	chr16:30759178-30759228	HEEpiC	esophagus:	n/a
33	chr16:30759573-30759623	AG09319	gingival:	n/a
34	chr16:30759675-30759725	HCM	heart:	n/a
35	chr16:30760244-30760294	AG10803	skin:	n/a
36	chr16:30759441-30759491	SK-N-SH_RA	brain:	n/a
37	chr16:30759573-30759623	AG09309	skin:	n/a
38	chr16:30759608-30759658	NH-A	brain:	n/a
39	chr16:30759310-30759360	RPTEC	kidney:	n/a
40	chr16:30759310-30759360	MCF-7	breast:	n/a
41	chr16:30759441-30759491	SAEC	small airway:	n/a
42	chr16:30759441-30759491	NHDF-neo	bronchial:	n/a
43	chr16:30760815-30760865	HPAEpiC	pulmonary alveolar:	n/a
44	chr16:30760186-30760236	AoSMC	blood vessel:	n/a
45	chr16:30760186-30760236	K562	blood:	n/a
46	chr16:30759703-30759753	T-47D	breast:	n/a
47	chr16:30759310-30759360	Hepatocyte	liver:	n/a
48	chr16:30759441-30759491	HRCEpiC	kidney:	n/a
49	chr16:30759675-30759725	HPAEpiC	pulmonary alveolar:	n/a
50	chr16:30759608-30759658	Hepatocyte	liver:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr16:30759018..30761215-chr16:30796843..30799156,2	MCF-7	breast:
2	chr16:30738148..30741438-chr16:30755814..30759116,3	K562	blood:
3	chr16:30757630..30759751-chr16:30932681..30935536,3	K562	blood:
4	chr16:30756860..30759445-chr16:30904243..30907032,3	K562	blood:
5	chr16:30669439..30671139-chr16:30758137..30761003,2	K562	blood:
6	chr16:30757885..30759765-chr16:30885602..30888334,3	MCF-7	breast:
7	chr16:30708929..30712034-chr16:30758251..30761730,4	K562	blood:
8	chr16:30749452..30756439-chr16:30756844..30761929,14	K562	blood:
9	chr16:30670863..30673913-chr16:30759873..30762559,3	MCF-7	breast:
10	chr16:30667897..30670733-chr16:30759554..30761748,2	K562	blood:
11	chr16:30759480..30761817-chr16:30958726..30961352,2	MCF-7	breast:
12	chr16:30671281..30672965-chr16:30757112..30759562,2	MCF-7	breast:
13	chr16:30757799..30759751-chr16:30933800..30935636,3	K562	blood:
14	chr16:30669453..30671146-chr16:30759344..30760999,2	MCF-7	breast:
15	chr16:30723735..30725867-chr16:30757899..30759500,2	MCF-7	breast:
16	chr16:30707181..30712037-chr16:30757231..30762842,12	MCF-7	breast:
17	chr16:30758787..30760683-chr16:30905572..30907460,2	MCF-7	breast:
18	chr16:30758359..30761183-chr16:30932981..30935164,3	MCF-7	breast:
19	chr1:64059379..64059995-chr16:30759447..30760265,2	Hela-S3	cervix:
20	chr16:30757305..30759426-chr16:30951863..30953472,2	MCF-7	breast:
21	chr16:30709802..30712559-chr16:30757474..30761628,7	MCF-7	breast:
22	chr16:30708001..30712248-chr16:30758568..30761366,5	K562	blood:
23	chr16:30759065..30761528-chr16:30906450..30908466,3	MCF-7	breast:

No data

Variant related genes	Relation type
PHKG2	TF binding region
PHKG2	CpG island
ENSG00000211591	chromatin interactions
ENSG00000142856	chromatin interactions
ENSG00000156860	chromatin interactions
ENSG00000260083	chromatin interactions
ENSG00000261840	chromatin interactions
ENSG00000262721	chromatin interactions
ENSG00000150281	chromatin interactions
ENSG00000261487	chromatin interactions
ENSG00000260899	chromatin interactions
ENSG00000079739	chromatin interactions
ENSG00000080603	chromatin interactions
ENSG00000099364	chromatin interactions
ENSG00000175938	chromatin interactions
ENSG00000260852	chromatin interactions
ENSG00000102870	chromatin interactions
ENSG00000265991	chromatin interactions
ENSG00000099385	chromatin interactions

Extended variants
information (count: 129 )
Associated
traits (count: 119 )

Variant overlapped rSNPs/rCNVs (count:129 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs184878388	chr16:30758920-30758921	Active TSS Weak transcription Enhancers Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
2	rs536863819	chr16:30758981-30758982	Active TSS Weak transcription Enhancers Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
3	rs554818943	chr16:30759016-30759017	Active TSS Flanking Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
4	rs144795626	chr16:30759018-30759019	Active TSS Flanking Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
5	rs540760148	chr16:30759043-30759044	Active TSS Flanking Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
6	rs552576978	chr16:30759045-30759046	Active TSS Flanking Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
7	rs113398868	chr16:30759126-30759127	Active TSS Flanking Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
8	rs544569398	chr16:30759134-30759135	Active TSS Flanking Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
9	rs568143928	chr16:30759158-30759159	Active TSS Flanking Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
10	rs148556572	chr16:30759216-30759217	Active TSS Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
11	rs35154691	chr16:30759243-30759244	Active TSS Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
12	rs563249865	chr16:30759255-30759256	Active TSS Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
13	rs540536836	chr16:30759267-30759268	Active TSS Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
14	rs34105831	chr16:30759292-30759293	Active TSS Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
15	rs552381358	chr16:30759328-30759329	Active TSS Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
16	rs530668751	chr16:30759341-30759342	Active TSS Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
17	rs12930519	chr16:30759388-30759389	Active TSS Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
18	rs12917856	chr16:30759389-30759390	Active TSS Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
19	rs542852510	chr16:30759441-30759442	Active TSS Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS Enhancers	TF binding region CpG island Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
20	rs113901228	chr16:30759449-30759450	Active TSS Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS Enhancers	TF binding region CpG island Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
21	rs535754778	chr16:30759470-30759471	Active TSS Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS Enhancers	TF binding region CpG island Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
22	rs546759178	chr16:30759500-30759501	Active TSS Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	17 gene(s)	Overlapped CNVs	n/a
23	rs571744992	chr16:30759519-30759520	Active TSS Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS Enhancers	TF binding region CpG island Chromatin interactive region	17 gene(s)	Overlapped CNVs	n/a
24	rs4889503	chr16:30759548-30759549	Active TSS Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS Enhancers	TF binding region CpG island Chromatin interactive region	17 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs550955974	chr16:30759579-30759580	Active TSS Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS Enhancers	TF binding region CpG island Chromatin interactive region	17 gene(s)	Overlapped CNVs	n/a
26	rs374629389	chr16:30759590-30759591	Active TSS Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS Enhancers	TF binding region CpG island Chromatin interactive region	17 gene(s)	Overlapped CNVs	n/a
27	rs569575367	chr16:30759610-30759611	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region CpG island Chromatin interactive region	17 gene(s)	Overlapped CNVs	n/a
28	rs536542470	chr16:30759684-30759685	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region CpG island Chromatin interactive region	17 gene(s)	Overlapped CNVs	n/a
29	rs11863277	chr16:30759716-30759717	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region CpG island Chromatin interactive region	17 gene(s)	Overlapped CNVs	n/a
30	rs566930196	chr16:30759721-30759722	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region CpG island Chromatin interactive region	17 gene(s)	Overlapped CNVs	n/a
31	rs112201430	chr16:30759779-30759780	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
32	rs556945561	chr16:30759802-30759803	Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
33	rs11547255	chr16:30759807-30759808	Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
34	rs534374752	chr16:30759809-30759810	Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
35	rs552665142	chr16:30759816-30759817	Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
36	rs577277206	chr16:30759836-30759837	Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
37	rs544606241	chr16:30759837-30759838	Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
38	rs575197046	chr16:30759878-30759879	Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
39	rs371557440	chr16:30759918-30759919	Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
40	rs575532264	chr16:30759922-30759923	Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
41	rs374019460	chr16:30760000-30760001	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Weak transcription	TF binding region Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
42	rs542539783	chr16:30760013-30760014	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
43	rs561168217	chr16:30760027-30760028	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
44	rs528299500	chr16:30760031-30760032	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
45	rs540396353	chr16:30760059-30760060	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
46	rs11547256	chr16:30760128-30760129	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
47	rs565389823	chr16:30760153-30760154	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
48	rs200427925	chr16:30760162-30760163	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
49	rs375063162	chr16:30760163-30760164	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
50	rs545856509	chr16:30760238-30760239	Active TSS Flanking Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:119)

Disease	PMID	Source
Hodgkin''s lymphoma	20651079	CNVD
Metanephric adenoma	20802469	CNVD
Melanoma	18172304	CNVD
Breast cancer	16608533	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17133270	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Lung adenocarcinoma	17086460	CNVD
Lung cancer	17086460	CNVD
Autism	22566537	CNVD
Intellectual disability	22566537	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Endometrial cancer	22040021	CNVD
Ewing''s sarcoma	21437220	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	17603634	CNVD
Breast cancer	21264507	CNVD
Cervical cancer	21063398	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Autism	19415332	CNVD
Medulloblastoma	21979893	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Schizophrenia	22958593	CNVD
Lung cancer	18438408	CNVD
Ductal carcinoma	22052326	CNVD
Breast cancer	21509527	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Hodgkin''s lymphoma	17606441	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	21858162	CNVD
Hepatocellular carcinoma	16750200	CNVD
Mental retardation	19951919	CNVD
Colorectal cancer	16272173	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Bladder cancer	21909424	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21785460	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Breast cancer	21990379	CNVD
Astrocytoma	22246337	CNVD
Myelofibrosis	22110671	CNVD
Epilepsy	22499536	CNVD
Attention deficit hyperactivity disorder	21324949	CNVD
Austim spectrum disorder	21302340	CNVD
Autism	22513405	CNVD
Autism	22958593	CNVD
Autism	18184952	CNVD
Autism	19966786	CNVD
Autism	21394203	CNVD
Autism	21969575	CNVD
Autism	22241247	CNVD
Autism	20970697	CNVD
Autism	20942916	CNVD
Epilepsy	20970697	CNVD
Intellectual disability	22045946	CNVD
Mental retardation	19966786	CNVD
Developmental delay	20808231	CNVD
Obesity	20808231	CNVD
Autism	18923514	CNVD
Obesity	21881559	CNVD
Obesity	21956041	CNVD
Autism	20659124	CNVD
Mental retardation	21062444	CNVD
Schizophrenia	20587603	CNVD
Schizophrenia	21285140	CNVD
Schizophrenia	22885689	CNVD
Schizophrenia	20553308	CNVD
Schizophrenia	20970697	CNVD
Schizophrenia	20433910	CNVD
Schizophrenia	22241247	CNVD
Autism	19242545	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Intracranial ependymoma	16609018	CNVD
Schizophrenia	21399695	CNVD
Autism	21956041	CNVD
Disorders of sex development	21048976	CNVD
Autism	22067053	CNVD
Autism	18156158	CNVD
Mental retardation	20152051	CNVD
Autism	19218893	CNVD
Autism	21289514	CNVD
Schizophrenia	19855392	CNVD
neurodevelopmental Syndrome	20503337	CNVD
Benign familial neonatal-infantile seizures	21060786	CNVD
Low-grade fibromyxoid sarcoma	0	CNVD
Cancer	21183584	CNVD
Low-grade fibromyxoid sarcoma	21536545	CNVD
Breast cancer	21045282	CNVD
Neuroblastoma	20406844	CNVD
Autism	19050728	CNVD
Epilepsy	20923578	CNVD
Psychiatric disorder	19050728	CNVD
Schizophrenia	19348701	CNVD
Attention deficit hyperactivity disorder	19097825	CNVD
Autism	20964600	CNVD
Schizophrenia	19955444	CNVD
Schizophrenia	18990708	CNVD
Schizophrenia	19571808	CNVD
Breast cancer	20409316	CNVD
Severe combined immunodeficiency	19097825	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Autism	18522746	CNVD
Urothelial carcinoma	21177765	CNVD
Chronic myeloid leukemia	21384125	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:616 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:30741000-30759000	Weak transcription	Fetal Brain Male	brain
2	chr16:30749800-30759000	Weak transcription	Pancreatic Islets	Pancreatic Islet
3	chr16:30750600-30759000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
4	chr16:30751000-30759000	Weak transcription	H9 Cell Line	embryonic stem cell
5	chr16:30751000-30759000	Weak transcription	Small Intestine	intestine
6	chr16:30751200-30759000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
7	chr16:30752400-30759000	Weak transcription	Fetal Kidney	kidney
8	chr16:30753200-30759000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
9	chr16:30753200-30759000	Weak transcription	Aorta	Aorta
10	chr16:30753400-30759200	Weak transcription	Gastric	stomach
11	chr16:30753800-30759000	Weak transcription	Right Ventricle	heart
12	chr16:30755600-30759000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
13	chr16:30755600-30759200	Weak transcription	Ovary	ovary
14	chr16:30755800-30759000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
15	chr16:30755800-30759000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
16	chr16:30755800-30759000	Weak transcription	Lung	lung
17	chr16:30755800-30759000	Weak transcription	Placenta Amnion	Placenta Amnion
18	chr16:30756600-30759000	Weak transcription	HUES6 Cell Line	embryonic stem cell
19	chr16:30756600-30759000	Weak transcription	HUES64 Cell Line	embryonic stem cell
20	chr16:30756600-30759000	Weak transcription	Cortex derived primary cultured neurospheres	brain
21	chr16:30756800-30759000	Weak transcription	H1 Cell Line	embryonic stem cell
22	chr16:30756800-30759000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
23	chr16:30756800-30759000	Weak transcription	Left Ventricle	heart
24	chr16:30757000-30759000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
25	chr16:30757000-30759000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
26	chr16:30757000-30759000	Weak transcription	HUES48 Cell Line	embryonic stem cell
27	chr16:30757000-30759000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
28	chr16:30757000-30759000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
29	chr16:30757000-30759000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
30	chr16:30757000-30759000	Weak transcription	Brain Inferior Temporal Lobe	brain
31	chr16:30757000-30759000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
32	chr16:30757000-30759000	Weak transcription	Fetal Lung	lung
33	chr16:30757000-30759000	Weak transcription	Fetal Muscle Trunk	muscle
34	chr16:30757000-30759000	Weak transcription	Placenta	Placenta
35	chr16:30757200-30759000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
36	chr16:30758000-30759000	Enhancers	Primary monocytes fromperipheralblood	blood
37	chr16:30758000-30759000	Enhancers	Muscle Satellite Cultured Cells	--
38	chr16:30758000-30759000	Enhancers	Liver	Liver
39	chr16:30758000-30759000	Enhancers	Duodenum Mucosa	Duodenum
40	chr16:30758000-30759000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
41	chr16:30758000-30759000	Enhancers	HMEC	breast
42	chr16:30758200-30759000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
43	chr16:30758200-30759000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
44	chr16:30758200-30759000	Enhancers	Primary neutrophils fromperipheralblood	blood
45	chr16:30758200-30759000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
46	chr16:30758200-30759000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
47	chr16:30758200-30759000	Enhancers	Osteobl	bone
48	chr16:30758600-30759000	Enhancers	Fetal Intestine Small	intestine
49	chr16:30758600-30759000	Enhancers	Stomach Mucosa	stomach
50	chr16:30758600-30759000	Enhancers	NH-A	brain

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