Variant report

Variant	nsv546163
Chromosome Location	chr1:46808042-46809782
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:63)
CpG islands
(count:61)
Chromatin interactive
region (count:6)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:63 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr1:46807601-46808132	GM12878	blood:	n/a	n/a
2	ATF2	chr1:46807715-46808136	GM12878	blood:	n/a	n/a
3	BHLHE40	chr1:46808011-46808054	K562	blood:	n/a	n/a
4	CHD2	chr1:46807465-46808224	GM12878	blood:	n/a	n/a
5	CTCF	chr1:46807697-46808186	GM12878	blood:	n/a	n/a
6	CTCF	chr1:46807900-46808050	NB4	blood:	n/a	n/a
7	CTCF	chr1:46807900-46808050	WERI-Rb-1	eye:	n/a	n/a
8	CTCF	chr1:46807636-46808222	A549	lung:	n/a	n/a
9	CTCF	chr1:46807721-46808051	H1-hESC	embryonic stem cell:	n/a	n/a
10	CTCF	chr1:46807900-46808050	GM12870	blood:	n/a	n/a
11	CTCF	chr1:46808060-46808210	NHLF	lung:	n/a	n/a
12	CTCF	chr1:46809200-46809350	GM12864	blood:	n/a	n/a
13	CTCF	chr1:46807731-46808085	IMR90	lung:	n/a	n/a
14	CTCF	chr1:46807960-46808110	BE2_C	brain:	n/a	n/a
15	CTCF	chr1:46808200-46808350	HPAF	blood vessel:	n/a	n/a
16	CTCF	chr1:46807920-46808070	HEEpiC	esophagus:	n/a	n/a
17	CTCF	chr1:46809360-46809510	GM12864	blood:	n/a	n/a
18	CTCF	chr1:46807734-46808084	K562	blood:	n/a	n/a
19	CTCF	chr1:46807784-46808190	K562	blood:	n/a	n/a
20	CUX1	chr1:46807674-46808494	GM12878	blood:	n/a	n/a
21	EBF1	chr1:46807424-46809213	GM12878	blood:	n/a	n/a
22	EBF1	chr1:46807741-46808762	GM12878	blood:	n/a	n/a
23	EBF1	chr1:46807754-46808386	GM12878	blood:	n/a	n/a
24	HEY1	chr1:46807364-46808174	K562	blood:	n/a	n/a
25	HEY1	chr1:46808354-46809141	K562	blood:	n/a	n/a
26	IRF4	chr1:46807910-46808406	GM12878	blood:	n/a	n/a
27	MAZ	chr1:46807767-46808124	GM12878	blood:	n/a	n/a
28	MAZ	chr1:46807607-46808223	IMR90	lung:	n/a	n/a
29	MTA3	chr1:46807670-46808299	GM12878	blood:	n/a	n/a
30	MXI1	chr1:46805301-46808164	SK-N-SH	brain:	n/a	n/a
31	MXI1	chr1:46805992-46808104	IMR90	lung:	n/a	n/a
32	PAX5	chr1:46807815-46808095	GM12878	blood:	n/a	n/a
33	POLR2A	chr1:46808341-46808710	HepG2	liver:	n/a	n/a
34	POLR2A	chr1:46809286-46809347	GM12878	blood:	n/a	n/a
35	POLR2A	chr1:46807922-46808581	Hela-S3	cervix:	n/a	n/a
36	POLR2A	chr1:46807477-46808169	K562	blood:	n/a	n/a
37	POLR2A	chr1:46809059-46809485	Hela-S3	cervix:	n/a	n/a
38	POLR2A	chr1:46809484-46809587	MCF10A-Er-Src	breast:	n/a	n/a
39	POLR2A	chr1:46808517-46808695	K562	blood:	n/a	n/a
40	POLR2A	chr1:46809018-46809693	K562	blood:	n/a	n/a
41	POLR2A	chr1:46809579-46809892	GM12878	blood:	n/a	n/a
42	POLR2A	chr1:46809447-46809822	K562	blood:	n/a	n/a
43	POLR2A	chr1:46807995-46808349	K562	blood:	n/a	n/a
44	POLR2A	chr1:46809537-46809781	HepG2	liver:	n/a	n/a
45	POLR2A	chr1:46809601-46809605	MCF10A-Er-Src	breast:	n/a	n/a
46	POLR2A	chr1:46809539-46809886	K562	blood:	n/a	n/a
47	POLR2A	chr1:46805002-46809990	K562	blood:	n/a	n/a
48	POLR2A	chr1:46805856-46808690	GM12878	blood:	n/a	n/a
49	POLR2A	chr1:46808184-46809855	K562	blood:	n/a	n/a
50	POLR2A	chr1:46808178-46808256	K562	blood:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:46809349-46809399	HPAEpiC	pulmonary alveolar:	n/a
2	chr1:46809349-46809399	SK-N-MC	brain:	n/a
3	chr1:46809349-46809399	ovcar-3	ovarian:	n/a
4	chr1:46809349-46809399	SK-N-SH_RA	brain:	n/a
5	chr1:46809349-46809399	PFSK-1	brain:	n/a
6	chr1:46809349-46809399	AG04450	lung:	fetal
7	chr1:46809349-46809399	A549	lung:	n/a
8	chr1:46809349-46809399	AG09319	gingival:	n/a
9	chr1:46809349-46809399	LNCaP	prostate:	n/a
10	chr1:46809349-46809399	NH-A	brain:	n/a
11	chr1:46809349-46809399	HMEC	breast:	n/a
12	chr1:46809349-46809399	HCPEpiC	choroid plexus:	n/a
13	chr1:46809349-46809399	HNPCEpiC	eye:	n/a
14	chr1:46809349-46809399	NT2-D1	testis:	n/a
15	chr1:46809349-46809399	NB4	blood:	n/a
16	chr1:46809349-46809399	K562	blood:	n/a
17	chr1:46809349-46809399	GM12891	blood:	n/a
18	chr1:46809349-46809399	NHBE	bronchial:	n/a
19	chr1:46809349-46809399	SKMC	muscle:	n/a
20	chr1:46809349-46809399	ECC-1	luminal epithelium:	n/a
21	chr1:46809349-46809399	HL-60	blood:	n/a
22	chr1:46809349-46809399	Hela-S3	cervix:	n/a
23	chr1:46809349-46809399	HIPEpiC	eye:	n/a
24	chr1:46809349-46809399	GM06990	blood:	n/a
25	chr1:46809349-46809399	Caco-2	colon:	n/a
26	chr1:46809349-46809399	IMR90	lung:	fetal
27	chr1:46809349-46809399	HRCEpiC	kidney:	n/a
28	chr1:46809349-46809399	SK-N-SH	brain:	n/a
29	chr1:46809349-46809399	ProgFib	skin:	n/a
30	chr1:46809349-46809399	BE2_C	brain:	n/a
31	chr1:46809349-46809399	HEK293	kidney:	embryo
32	chr1:46809349-46809399	H1-hESC	embryonic stem cell:	embryo
33	chr1:46809349-46809399	GM19239	blood:	n/a
34	chr1:46809349-46809399	PANC-1	pancreas:	n/a
35	chr1:46809349-46809399	HCF	heart:	n/a
36	chr1:46809349-46809399	NHDF-neo	bronchial:	n/a
37	chr1:46809349-46809399	Hepatocyte	liver:	n/a
38	chr1:46809349-46809399	MCF-7	breast:	n/a
39	chr1:46809349-46809399	SAEC	small airway:	n/a
40	chr1:46809349-46809399	GM12878	blood:	n/a
41	chr1:46809349-46809399	HepG2	liver:	n/a
42	chr1:46809349-46809399	GM12892	blood:	n/a
43	chr1:46809349-46809399	Jurkat	blood:	n/a
44	chr1:46809349-46809399	MCF10A-Er-Src	breast:	n/a
45	chr1:46809349-46809399	HCT-116	colon:	n/a
46	chr1:46809349-46809399	AG10803	skin:	n/a
47	chr1:46809349-46809399	HCM	heart:	n/a
48	chr1:46809349-46809399	BJ	skin:	n/a
49	chr1:46809349-46809399	AG04449	skin:	fetal
50	chr1:46809349-46809399	HEEpiC	esophagus:	n/a

(count:6 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:46775398..46777226-chr1:46806955..46809185,2	K562	blood:
2	chr1:46711376..46714616-chr1:46809094..46811770,3	K562	blood:
3	chr1:46711990..46716191-chr1:46804369..46808176,4	K562	blood:
4	chr1:46649178..46652657-chr1:46804646..46808340,3	K562	blood:
5	chr1:46763061..46775715-chr1:46803221..46815018,50	K562	blood:
6	chr1:46763061..46775205-chr1:46803159..46817121,53	K562	blood:

No data

Variant related genes	Relation type
NSUN4	TF binding region
NSUN4	CpG island
ENSG00000117472	chromatin interactions
ENSG00000085999	chromatin interactions
ENSG00000173660	chromatin interactions
ENSG00000132128	chromatin interactions

Extended variants
information (count: 60 )
Associated
traits (count: 95 )

Variant overlapped rSNPs/rCNVs (count:60 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs12563610	chr1:46808042-46808043	Weak transcription Strong transcription Genic enhancers Enhancers Active TSS Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs78467752	chr1:46808055-46808056	Weak transcription Strong transcription Genic enhancers Enhancers Active TSS Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
3	rs529886729	chr1:46808060-46808061	Weak transcription Strong transcription Genic enhancers Enhancers Active TSS Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
4	rs575227693	chr1:46808093-46808094	Weak transcription Strong transcription Genic enhancers Enhancers Active TSS Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
5	rs548351406	chr1:46808180-46808181	Weak transcription Strong transcription Genic enhancers Enhancers Active TSS Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
6	rs367782847	chr1:46808194-46808195	Weak transcription Strong transcription Genic enhancers Enhancers Active TSS Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
7	rs149294298	chr1:46808200-46808201	Weak transcription Strong transcription Genic enhancers Enhancers Active TSS Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
8	rs144564318	chr1:46808221-46808222	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
9	rs56909107	chr1:46808224-46808225	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
10	rs537804421	chr1:46808242-46808243	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
11	rs374806217	chr1:46808252-46808253	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
12	rs368232702	chr1:46808253-46808254	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
13	rs556429600	chr1:46808278-46808279	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
14	rs568534036	chr1:46808292-46808293	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
15	rs536861203	chr1:46808296-46808297	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
16	rs114109092	chr1:46808363-46808364	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs182979897	chr1:46808377-46808378	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs41293285	chr1:46808426-46808427	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
19	rs572640617	chr1:46808431-46808432	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs17357628	chr1:46808462-46808463	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
21	rs188991877	chr1:46808509-46808510	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs368046158	chr1:46808518-46808519	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs576960161	chr1:46808527-46808528	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs148461706	chr1:46808564-46808565	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs17357635	chr1:46808668-46808669	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
26	rs68191463	chr1:46808695-46808696	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
27	rs376289843	chr1:46808727-46808728	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs559931346	chr1:46808769-46808770	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs527443539	chr1:46808772-46808773	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs552059721	chr1:46808783-46808784	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs34752107	chr1:46808818-46808819	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs41293287	chr1:46808852-46808853	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
33	rs76976909	chr1:46808858-46808859	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs56126529	chr1:46808860-46808861	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
35	rs71572611	chr1:46808868-46808869	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs550125544	chr1:46808876-46808877	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs369313619	chr1:46808909-46808910	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs184451539	chr1:46808939-46808940	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs535957314	chr1:46808955-46808956	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs547868548	chr1:46809012-46809013	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs11802856	chr1:46809016-46809017	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs7525309	chr1:46809025-46809026	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
43	rs187597617	chr1:46809086-46809087	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs144132611	chr1:46809140-46809141	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
45	rs191638634	chr1:46809161-46809162	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
46	rs537473168	chr1:46809170-46809171	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
47	rs556146916	chr1:46809248-46809249	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
48	rs76008820	chr1:46809271-46809272	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
49	rs541918905	chr1:46809283-46809284	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
50	rs7548675	chr1:46809321-46809322	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance

Variant related diseases (count:95)

Disease	PMID	Source
Glioblastoma multiforme	21080181	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	17603634	CNVD
Soft tissue tumor	16732325	CNVD
Papillary thyroid carcinoma	21436994	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Colorectal cancer	16272173	CNVD
Wilms tumour	21544195	CNVD
Coronary Disease	20032323	CNVD
Prostate cancer	21965145	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Stargardt''s disease	17277736	CNVD
Neuroblastoma	17897457	CNVD
Uveal melanoma	21693616	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	21484798	CNVD
Non-syndromic sensorineural hearing loss	22290220	CNVD
Liposarcoma	21253554	CNVD
Breast cancer	21264507	CNVD
Acute myeloid leukemia	16864856	CNVD
Astrocytoma	17387387	CNVD
Cancer	21499728	CNVD
Glioblastoma multiforme	17387387	CNVD
Oligodendroglial tumors	17285580	CNVD
Neuroblastoma	17535989	CNVD
Pheochromocytoma	17535989	CNVD
Prostate cancer	16705090	CNVD
Astrocytoma	17934521	CNVD
Colorectal cancer	19359472	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Neuroblastoma	17533364	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Chronic myeloid leukemia	21384125	CNVD
Prostate cancer	18632612	CNVD
Autism	22495311	CNVD
Non-small cell lung cancer	21385341	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Chordoma	21602918	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Melanoma	18172304	CNVD
Multiple myeloma	16461302	CNVD
Melanoma	17363583	CNVD
Cancer	21129771	CNVD
Autosomal dominant nocturnal frontal lobe epilepsy	18472482	CNVD
Hirschsprung''s Disease	21712996	CNVD
Non-small cell lung cancer	20864512	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Thrombocytopenia-absent radius syndrome	21933853	CNVD
Psychiatric disorder	22848183	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	20409316	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Lung cancer	18438408	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17393978	CNVD
Cervical cancer	21062161	CNVD
Cancer	21183584	CNVD
Muscle-eye-brain disease	21572526	CNVD
Breast cancer	21785460	CNVD
Myelofibrosis	22110671	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21364760	CNVD
Neuroblastoma	21899760	CNVD
Uveal melanoma	20484589	CNVD
Malignant fibrous histiocytomas	21085701	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	22522925	CNVD
Glioblastoma	20031968	CNVD
Leukemia	18688285	CNVD

Chromatin state (count:223 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:46805600-46808200	Active TSS	iPS-15b Cell Line	embryonic stem cell
2	chr1:46807000-46808800	Genic enhancers	Primary B cells from peripheral blood	blood
3	chr1:46807000-46810000	Enhancers	Fetal Heart	heart
4	chr1:46807000-46827200	Weak transcription	Fetal Brain Male	brain
5	chr1:46807200-46808200	Enhancers	Primary T helper naive cells fromperipheralblood	blood
6	chr1:46807200-46808400	Weak transcription	Primary T cells from cord blood	blood
7	chr1:46807200-46808400	Enhancers	Primary T cells fromperipheralblood	blood
8	chr1:46807200-46808400	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
9	chr1:46807200-46808400	Transcr. at gene 5' and 3'	Foreskin Fibroblast Primary Cells skin01	Skin
10	chr1:46807200-46808600	Flanking Active TSS	GM12878-XiMat	blood
11	chr1:46807200-46808800	Weak transcription	Ovary	ovary
12	chr1:46807200-46809400	Enhancers	Left Ventricle	heart
13	chr1:46807200-46809400	Weak transcription	Thymus	Thymus
14	chr1:46807200-46810200	Weak transcription	Aorta	Aorta
15	chr1:46807200-46810600	Weak transcription	Fetal Kidney	kidney
16	chr1:46807200-46818400	Weak transcription	Small Intestine	intestine
17	chr1:46807200-46827600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
18	chr1:46807400-46808200	Enhancers	Right Ventricle	heart
19	chr1:46807400-46808400	Weak transcription	Lung	lung
20	chr1:46807400-46808800	Genic enhancers	Placenta	Placenta
21	chr1:46807400-46809200	Weak transcription	Placenta Amnion	Placenta Amnion
22	chr1:46807400-46809400	Genic enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
23	chr1:46807400-46809400	Genic enhancers	Fetal Muscle Trunk	muscle
24	chr1:46807400-46809400	Genic enhancers	Fetal Muscle Leg	muscle
25	chr1:46807400-46809400	Weak transcription	Rectal Mucosa Donor 31	rectum
26	chr1:46807400-46810200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
27	chr1:46807400-46810200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
28	chr1:46807400-46810600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
29	chr1:46807400-46813200	Weak transcription	Primary neutrophils fromperipheralblood	blood
30	chr1:46807400-46815200	Weak transcription	Pancreatic Islets	Pancreatic Islet
31	chr1:46807400-46820400	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
32	chr1:46807400-46831800	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
33	chr1:46807400-46832200	Strong transcription	Fetal Stomach	stomach
34	chr1:46807600-46808200	Strong transcription	H9 Cell Line	embryonic stem cell
35	chr1:46807600-46808200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
36	chr1:46807600-46808200	Transcr. at gene 5' and 3'	K562	blood
37	chr1:46807600-46808200	Enhancers	NH-A	brain
38	chr1:46807600-46808400	Weak transcription	Sigmoid Colon	Sigmoid Colon
39	chr1:46807600-46808400	Genic enhancers	Skeletal Muscle Female	skeletal muscle
40	chr1:46807600-46808400	Transcr. at gene 5' and 3'	Dnd41	blood
41	chr1:46807600-46808400	Enhancers	HMEC	breast
42	chr1:46807600-46808600	Genic enhancers	Primary hematopoietic stem cells short term culture	blood
43	chr1:46807600-46808800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
44	chr1:46807600-46808800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
45	chr1:46807600-46808800	Weak transcription	Rectal Smooth Muscle	rectum
46	chr1:46807600-46809200	Weak transcription	Rectal Mucosa Donor 29	rectum
47	chr1:46807600-46809400	Weak transcription	Fetal Brain Female	brain
48	chr1:46807600-46809600	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
49	chr1:46807600-46809600	Weak transcription	Brain Germinal Matrix	brain
50	chr1:46807600-46809600	Weak transcription	Brain Substantia Nigra	brain

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