Variant report

Variant	nsv437213
Chromosome Location	chr1:160652730-160681836
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:634)
CpG islands
(count:244)
Chromatin interactive
region (count:9)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:634 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr1:160680967-160682290	GM12878	blood:	n/a	n/a
2	ATF2	chr1:160680144-160682239	GM12878	blood:	n/a	n/a
3	ATF2	chr1:160677062-160678428	GM12878	blood:	n/a	n/a
4	ATF2	chr1:160677585-160678898	GM12878	blood:	n/a	n/a
5	ATF2	chr1:160678525-160679568	GM12878	blood:	n/a	n/a
6	BATF	chr1:160677787-160678311	GM12878	blood:	n/a	n/a
7	BCL3	chr1:160681263-160682064	GM12878	blood:	n/a	n/a
8	BCLAF1	chr1:160680208-160682107	GM12878	blood:	n/a	n/a
9	BCLAF1	chr1:160676988-160678199	GM12878	blood:	n/a	chr1:160678110-160678119
10	BCLAF1	chr1:160678282-160679891	GM12878	blood:	n/a	chr1:160678848-160678857
11	BCLAF1	chr1:160676147-160682296	GM12878	blood:	n/a	chr1:160678848-160678857 chr1:160678110-160678119
12	BHLHE40	chr1:160681395-160681985	GM12878	blood:	n/a	n/a
13	BHLHE40	chr1:160662231-160662418	K562	blood:	n/a	n/a
14	BHLHE40	chr1:160678653-160679219	GM12878	blood:	n/a	n/a
15	BRCA1	chr1:160675256-160675313	GM12878	blood:	n/a	n/a
16	BRCA1	chr1:160652993-160653167	GM12878	blood:	n/a	n/a
17	CEBPB	chr1:160674237-160674443	A549	lung:	n/a	chr1:160674314-160674325
18	CEBPB	chr1:160674168-160674454	HepG2	liver:	n/a	chr1:160674314-160674325
19	CEBPB	chr1:160674197-160674427	Hela-S3	cervix:	n/a	chr1:160674314-160674325
20	CEBPB	chr1:160674159-160674377	IMR90	lung:	n/a	chr1:160674314-160674325
21	CEBPB	chr1:160680820-160681947	GM12878	blood:	n/a	chr1:160681630-160681642
22	CEBPB	chr1:160677438-160679216	GM12878	blood:	n/a	n/a
23	CEBPD	chr1:160662182-160662581	K562	blood:	n/a	n/a
24	CHD1	chr1:160673771-160673867	GM12878	blood:	n/a	n/a
25	CHD1	chr1:160676954-160682062	GM12878	blood:	n/a	n/a
26	CHD1	chr1:160674347-160674478	GM12878	blood:	n/a	n/a
27	CHD1	chr1:160676583-160676718	GM12878	blood:	n/a	n/a
28	CHD1	chr1:160674738-160674840	GM12878	blood:	n/a	n/a
29	CHD1	chr1:160675377-160675849	GM12878	blood:	n/a	n/a
30	CHD2	chr1:160654977-160655035	GM12878	blood:	n/a	n/a
31	CHD2	chr1:160681410-160681961	GM12878	blood:	n/a	n/a
32	CTCF	chr1:160662299-160662605	GM12878	blood:	n/a	n/a
33	CTCF	chr1:160675320-160675470	NB4	blood:	n/a	n/a
34	CTCF	chr1:160662340-160662490	GM12864	blood:	n/a	n/a
35	CTCF	chr1:160675560-160675710	GM12865	blood:	n/a	n/a
36	CTCF	chr1:160675600-160675750	GM12871	blood:	n/a	n/a
37	CTCF	chr1:160675300-160675450	GM12873	blood:	n/a	n/a
38	CTCF	chr1:160664752-160664800	K562	blood:	n/a	n/a
39	CTCF	chr1:160662367-160662455	GM19238	blood:	n/a	n/a
40	CTCF	chr1:160662342-160662523	MCF-7	breast:	n/a	n/a
41	CTCF	chr1:160679200-160679350	GM12869	blood:	n/a	n/a
42	CTCF	chr1:160662360-160662510	BE2_C	brain:	n/a	n/a
43	CTCF	chr1:160675520-160675670	GM12874	blood:	n/a	n/a
44	CTCF	chr1:160675520-160675670	GM12864	blood:	n/a	n/a
45	CTCF	chr1:160662373-160662542	Spleen_OC	spleen:	n/a	n/a
46	CTCF	chr1:160675579-160675718	MCF-7	breast:	n/a	n/a
47	CTCF	chr1:160662340-160662490	HRPEpiC	eye:	n/a	n/a
48	CTCF	chr1:160675500-160675650	MCF-7	breast:	n/a	n/a
49	CTCF	chr1:160662204-160662590	H1-hESC	embryonic stem cell:	n/a	n/a
50	CTCF	chr1:160675619-160675703	GM12892	blood:	n/a	n/a

(count:244 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:160681530-160681580	AG10803	skin:	n/a
2	chr1:160677398-160677448	HPAEpiC	pulmonary alveolar:	n/a
3	chr1:160681760-160681810	GM12891	blood:	n/a
4	chr1:160677398-160677448	Hela-S3	cervix:	n/a
5	chr1:160681404-160681454	MCF10A-Er-Src	breast:	n/a
6	chr1:160677398-160677448	NH-A	brain:	n/a
7	chr1:160681530-160681580	H1-hESC	embryonic stem cell:	embryo
8	chr1:160681530-160681580	HIPEpiC	eye:	n/a
9	chr1:160681760-160681810	BJ	skin:	n/a
10	chr1:160681404-160681454	HRPEpiC	eye:	n/a
11	chr1:160681760-160681810	K562	blood:	n/a
12	chr1:160677398-160677448	HCT-116	colon:	n/a
13	chr1:160677398-160677448	HAEpiC	amniotic membrane:	n/a
14	chr1:160681530-160681580	AoSMC	blood vessel:	n/a
15	chr1:160681404-160681454	AG04449	skin:	fetal
16	chr1:160681530-160681580	HL-60	blood:	n/a
17	chr1:160681404-160681454	AG10803	skin:	n/a
18	chr1:160681760-160681810	HPAEpiC	pulmonary alveolar:	n/a
19	chr1:160681760-160681810	HMEC	breast:	n/a
20	chr1:160677398-160677448	AG04449	skin:	fetal
21	chr1:160681530-160681580	SK-N-MC	brain:	n/a
22	chr1:160681530-160681580	BE2_C	brain:	n/a
23	chr1:160681530-160681580	Hela-S3	cervix:	n/a
24	chr1:160681760-160681810	AG09309	skin:	n/a
25	chr1:160681760-160681810	NHBE	bronchial:	n/a
26	chr1:160681760-160681810	H1-hESC	embryonic stem cell:	embryo
27	chr1:160677398-160677448	ProgFib	skin:	n/a
28	chr1:160681760-160681810	GM06990	blood:	n/a
29	chr1:160681530-160681580	HepG2	liver:	n/a
30	chr1:160677398-160677448	AG09319	gingival:	n/a
31	chr1:160681760-160681810	BE2_C	brain:	n/a
32	chr1:160681760-160681810	HCT-116	colon:	n/a
33	chr1:160681760-160681810	RPTEC	kidney:	n/a
34	chr1:160681404-160681454	HepG2	liver:	n/a
35	chr1:160681404-160681454	HCT-116	colon:	n/a
36	chr1:160681530-160681580	SK-N-SH_RA	brain:	n/a
37	chr1:160681530-160681580	RPTEC	kidney:	n/a
38	chr1:160681530-160681580	AG09309	skin:	n/a
39	chr1:160681404-160681454	HIPEpiC	eye:	n/a
40	chr1:160677398-160677448	HIPEpiC	eye:	n/a
41	chr1:160681404-160681454	SK-N-SH	brain:	n/a
42	chr1:160677398-160677448	BE2_C	brain:	n/a
43	chr1:160681760-160681810	HRCEpiC	kidney:	n/a
44	chr1:160681530-160681580	Caco-2	colon:	n/a
45	chr1:160681404-160681454	Hela-S3	cervix:	n/a
46	chr1:160677398-160677448	HCM	heart:	n/a
47	chr1:160677398-160677448	GM19239	blood:	n/a
48	chr1:160677398-160677448	PFSK-1	brain:	n/a
49	chr1:160681404-160681454	HMEC	breast:	n/a
50	chr1:160677398-160677448	K562	blood:	n/a

(count:9 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:160645135..160646248-chr1:160661915..160662860,3	MCF-7	breast:
2	chr1:160557184..160557879-chr1:160661976..160662561,2	MCF-7	breast:
3	chr1:160648911..160653245-chr1:160654061..160656331,4	K562	blood:
4	chr1:160655760..160657407-chr1:160694604..160697508,2	K562	blood:
5	chr1:160675860..160678038-chr1:160680233..160682705,2	K562	blood:
6	chr1:160645151..160645969-chr1:160668420..160668927,2	MCF-7	breast:
7	chr1:160648911..160653245-chr1:160654061..160656331,4	K562	blood:
8	chr1:160650970..160651890-chr1:160662246..160662875,3	MCF-7	breast:
9	chr1:160672794..160675348-chr1:161062304..161065279,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SLAMF7-2	chr1:160653389-160653698	ENSG00000228863.4
2	lnc-SLAMF7-2	chr1:160653389-160653612	ENSG00000228863.4
3	lnc-SLAMF7-6	chr1:160667984-160668001	NONHSAT007072
4	lnc-SLAMF7-8	chr1:160654221-160655316	NONHSAT007071
5	lnc-SLAMF7-6	chr1:160667760-160667978	NONHSAT007072
6	lnc-SLAMF7-2	chr1:160653389-160653612	ENSG00000228863.1

No data

Variant related genes	Relation type
CD48	TF binding region
ENSG00000227239	TF binding region
CD48	CpG island
ENSG00000227239	CpG island
ENSG00000117091	chromatin interactions

Extended variants
information (count: 1390 )
Associated
traits (count: 107 )

Variant overlapped rSNPs/rCNVs (count:1390 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs3796502	chr1:160652730-160652731	Weak transcription Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs573519356	chr1:160652732-160652733	Weak transcription Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs536351613	chr1:160652738-160652739	Weak transcription Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs552841674	chr1:160652769-160652770	Weak transcription Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs147380199	chr1:160652816-160652817	Weak transcription Genic enhancers Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs545249467	chr1:160652852-160652853	Weak transcription Genic enhancers Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs139413958	chr1:160652875-160652876	Weak transcription Genic enhancers Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs575622634	chr1:160652908-160652909	Weak transcription Genic enhancers Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs142530645	chr1:160652971-160652972	Weak transcription Genic enhancers Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs561337284	chr1:160653002-160653003	Weak transcription Enhancers Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs77471921	chr1:160653017-160653018	Weak transcription Enhancers Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs77232475	chr1:160653019-160653020	Weak transcription Enhancers Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs79798282	chr1:160653020-160653021	Weak transcription Enhancers Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs76099875	chr1:160653021-160653022	Weak transcription Enhancers Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs530085634	chr1:160653072-160653073	Weak transcription Enhancers Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs367719325	chr1:160653087-160653088	Weak transcription Enhancers Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs151008538	chr1:160653093-160653094	Weak transcription Enhancers Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs75869846	chr1:160653206-160653207	Weak transcription Genic enhancers Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs532447855	chr1:160653238-160653239	Weak transcription Genic enhancers Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs139644120	chr1:160653241-160653242	Weak transcription Genic enhancers Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs569077571	chr1:160653245-160653246	Weak transcription Genic enhancers Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs538543675	chr1:160653253-160653254	Weak transcription Genic enhancers Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs184404680	chr1:160653262-160653263	Weak transcription Genic enhancers Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs371473463	chr1:160653268-160653269	Weak transcription Genic enhancers Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs79281455	chr1:160653298-160653299	Weak transcription Genic enhancers Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs66994511	chr1:160653299-160653300	Weak transcription Genic enhancers Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs374949771	chr1:160653308-160653309	Weak transcription Genic enhancers Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs549934666	chr1:160653309-160653310	Weak transcription Genic enhancers Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs552910084	chr1:160653324-160653325	Weak transcription Genic enhancers Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs368080311	chr1:160653325-160653326	Weak transcription Genic enhancers Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs78934591	chr1:160653329-160653330	Weak transcription Genic enhancers Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs538701574	chr1:160653392-160653393	Weak transcription Genic enhancers Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
33	rs75100621	chr1:160653407-160653408	Weak transcription Genic enhancers Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
34	rs80110046	chr1:160653408-160653409	Weak transcription Genic enhancers Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
35	rs16832317	chr1:160653453-160653454	Weak transcription Genic enhancers Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs116437679	chr1:160653484-160653485	Weak transcription Genic enhancers Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
37	rs146715476	chr1:160653490-160653491	Weak transcription Genic enhancers Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
38	rs544390238	chr1:160653497-160653498	Weak transcription Genic enhancers Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
39	rs188650793	chr1:160653504-160653505	Weak transcription Genic enhancers Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
40	rs12139411	chr1:160653567-160653568	Weak transcription Genic enhancers Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs113981173	chr1:160653570-160653571	Weak transcription Genic enhancers Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
42	rs146819264	chr1:160653653-160653654	Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3' Flanking Active TSS Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
43	rs114499754	chr1:160653654-160653655	Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3' Flanking Active TSS Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
44	rs370991178	chr1:160653691-160653692	Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3' Flanking Active TSS Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
45	rs73012288	chr1:160653716-160653717	Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3' Flanking Active TSS Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs562750239	chr1:160653730-160653731	Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3' Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs200841796	chr1:160653757-160653758	Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3' Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs531859511	chr1:160653832-160653833	Weak transcription Genic enhancers Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs148928411	chr1:160653856-160653857	Weak transcription Genic enhancers Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs544309481	chr1:160653895-160653896	Weak transcription Genic enhancers Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:107)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Liposarcoma	21253554	CNVD
Non-small cell lung cancer	21385341	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	18698080	CNVD
Melanoma	18172304	CNVD
Cervical cancer	21062161	CNVD
Glioblastoma multiforme	21080181	CNVD
Cancer	21183584	CNVD
Multiple myeloma	16461302	CNVD
Lung cancer	18438408	CNVD
Rett syndrome	21593744	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Medulloblastoma	21979893	CNVD
Systemic lupus erythematosus	21956041	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	CNVD
Non-small cell lung cancer	21829676	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Non-small cell lung cancer	21044232	CNVD
Cervical cancer	21063398	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	20632083	CNVD
Endometrial cancer	22040021	CNVD
Ewing''s sarcoma	21437220	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Medulloblastoma	21292688	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	21264507	CNVD
Multiple myeloma	21628407	CNVD
Cancer	16751803	CNVD
Prostate cancer	16705090	CNVD
Neuroblastoma	19435921	CNVD
Breast cancer	17850661	CNVD
Breast cancer	16461572	CNVD
Intracranial tumor	16823260	CNVD
Medulloblastoma	18056178	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Colorectal cancer	16272173	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Neuroblastoma	21899760	CNVD
Breast cancer	17899364	CNVD
Bladder cancer	19088036	CNVD
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17002787	CNVD
Breast cancer	21858162	CNVD
Retinoblastoma	19183342	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	16608533	CNVD
Ewing''s sarcoma	22429812	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Type 2 diabetes	19141583	CNVD
Chordoma	18071362	CNVD
Hepatocellular carcinoma	18803288	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17001317	CNVD
Urothelial carcinoma	21177765	CNVD
Burkitt''s lymphoma	19759907	CNVD
Acute myeloid leukemia	21251322	CNVD
Multiple myeloma	17550852	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21509527	CNVD
Bladder cancer	21909424	CNVD
Acute myeloid leukemia	20729466	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Testicular germ cell tumor	18059402	CNVD
Trisomy 5 syndrome	21098271	CNVD
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Breast cancer	21611746	CNVD
Neuroblastoma	18923191	CNVD
Systemic lupus erythematosus	19220326	CNVD
Systemic lupus erythematosus	19287148	CNVD
Glomerulonephritis	19341492	CNVD
Systemic lupus erythematosus	18559452	CNVD
Systemic autoimmune disease	17597778	CNVD
Glomerulonephritis	17008540	CNVD
Glomerulonephritis	16482158	CNVD
Soft tissue tumor	16732325	CNVD
Cancer	17060936	CNVD
Lung cancer	16740712	CNVD
Breast cancer	21045282	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Ewing''s sarcoma	17952124	CNVD
Follicular lymphoma	18703704	CNVD
Myelofibrosis	22110671	CNVD
Intracranial ependymoma	16609018	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	20409316	CNVD
Mental retardation	17847001	CNVD
Idiopathic thrombocytopenic purpura	17827395	CNVD

Chromatin state (count:609 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:160643400-160655200	Weak transcription	Colonic Mucosa	Colon
2	chr1:160644600-160655800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
3	chr1:160645800-160653600	Weak transcription	Fetal Intestine Small	intestine
4	chr1:160646000-160653000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
5	chr1:160646000-160653000	Weak transcription	Rectal Mucosa Donor 31	rectum
6	chr1:160650400-160655600	Genic enhancers	Fetal Thymus	thymus
7	chr1:160650600-160656400	Genic enhancers	Primary T cells fromperipheralblood	blood
8	chr1:160650800-160652800	Genic enhancers	Primary T helper memory cells from peripheral blood 1	blood
9	chr1:160650800-160653000	Genic enhancers	Primary T killer naive cells fromperipheralblood	blood
10	chr1:160650800-160655200	Genic enhancers	Primary Natural Killer cells fromperipheralblood	blood
11	chr1:160651000-160653000	Genic enhancers	Primary T killer memory cells from peripheral blood	blood
12	chr1:160651000-160653200	Weak transcription	Lung	lung
13	chr1:160651000-160656400	Genic enhancers	Primary B cells from peripheral blood	blood
14	chr1:160651000-160656400	Genic enhancers	Primary T helper cells fromperipheralblood	blood
15	chr1:160651200-160652800	Weak transcription	Primary hematopoietic stem cells	blood
16	chr1:160651200-160653000	Genic enhancers	Primary T helper naive cells from peripheral blood	blood
17	chr1:160651200-160653200	Genic enhancers	Primary T regulatory cells fromperipheralblood	blood
18	chr1:160651200-160655000	Genic enhancers	Primary T helper naive cells fromperipheralblood	blood
19	chr1:160651200-160655800	Genic enhancers	Primary hematopoietic stem cells short term culture	blood
20	chr1:160651400-160656000	Genic enhancers	Primary B cells from cord blood	blood
21	chr1:160651600-160653800	Genic enhancers	GM12878-XiMat	blood
22	chr1:160651600-160655400	Genic enhancers	Primary mononuclear cells fromperipheralblood	Blood
23	chr1:160651600-160655400	Genic enhancers	Dnd41	blood
24	chr1:160651600-160656400	Genic enhancers	Primary T cells from cord blood	blood
25	chr1:160651600-160656600	Genic enhancers	Primary monocytes fromperipheralblood	blood
26	chr1:160651800-160653400	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
27	chr1:160651800-160653400	Enhancers	Duodenum Mucosa	Duodenum
28	chr1:160651800-160654200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
29	chr1:160651800-160654800	Strong transcription	Thymus	Thymus
30	chr1:160652200-160654200	Enhancers	Small Intestine	intestine
31	chr1:160652400-160653200	Flanking Active TSS	Primary T helper memory cells from peripheral blood 2	blood
32	chr1:160652400-160653200	Enhancers	Sigmoid Colon	Sigmoid Colon
33	chr1:160652600-160652800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
34	chr1:160652600-160653000	Weak transcription	Spleen	Spleen
35	chr1:160652600-160653200	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
36	chr1:160652600-160653600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
37	chr1:160652600-160653800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
38	chr1:160652600-160654000	Transcr. at gene 5' and 3'	Primary T helper cells PMA-I stimulated	--
39	chr1:160652600-160655000	Transcr. at gene 5' and 3'	Monocytes-CD14+_RO01746	blood
40	chr1:160652600-160655400	Transcr. at gene 5' and 3'	Primary T helper 17 cells PMA-I stimulated	--
41	chr1:160652600-160656000	Enhancers	Rectal Mucosa Donor 29	rectum
42	chr1:160652800-160653600	Flanking Active TSS	Primary T helper memory cells from peripheral blood 1	blood
43	chr1:160652800-160654000	Enhancers	Primary hematopoietic stem cells	blood
44	chr1:160653000-160653200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
45	chr1:160653000-160653200	Enhancers	Primary T killer memory cells from peripheral blood	blood
46	chr1:160653000-160653200	Enhancers	Rectal Mucosa Donor 31	rectum
47	chr1:160653000-160653200	Enhancers	Spleen	Spleen
48	chr1:160653000-160653400	Flanking Active TSS	Primary T helper naive cells from peripheral blood	blood
49	chr1:160653000-160653600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
50	chr1:160653000-160654200	Enhancers	Primary T killer naive cells fromperipheralblood	blood

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