Variant report

Variant	nsv1009313
Chromosome Location	chr1:169661299-169680173
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr1:169666839-169667373	GM12878	blood:	n/a	n/a
2	BATF	chr1:169668150-169668460	GM12878	blood:	n/a	n/a
3	BATF	chr1:169666902-169667269	GM12878	blood:	n/a	n/a
4	BHLHE40	chr1:169661404-169662555	GM12878	blood:	n/a	n/a
5	CHD1	chr1:169663513-169663645	GM12878	blood:	n/a	n/a
6	CTCF	chr1:169663440-169663852	MCF-7	breast:	n/a	chr1:169663577-169663585 chr1:169663572-169663590 chr1:169663567-169663588
7	CTCF	chr1:169669017-169669198	Medullo	brain:	n/a	n/a
8	CTCF	chr1:169663512-169663659	GM12878	blood:	n/a	chr1:169663577-169663585 chr1:169663572-169663590 chr1:169663567-169663588
9	CTCF	chr1:169663560-169663710	SAEC	small airway:	n/a	chr1:169663577-169663585 chr1:169663572-169663590 chr1:169663567-169663588
10	CTCF	chr1:169663493-169663708	MCF-7	breast:	n/a	chr1:169663577-169663585 chr1:169663572-169663590 chr1:169663567-169663588
11	CTCF	chr1:169663480-169663630	HMEC	breast:	n/a	chr1:169663577-169663585 chr1:169663572-169663590 chr1:169663567-169663588
12	CTCF	chr1:169663354-169663771	HCT-116	colon:	n/a	chr1:169663577-169663585 chr1:169663572-169663590 chr1:169663567-169663588
13	CTCF	chr1:169669040-169669190	Caco-2	colon:	n/a	n/a
14	CTCF	chr1:169663562-169663585	Lung_OC	lung:	n/a	chr1:169663577-169663585
15	CTCF	chr1:169663480-169663630	GM12867	blood:	n/a	chr1:169663577-169663585 chr1:169663572-169663590 chr1:169663567-169663588
16	CTCF	chr1:169663460-169663610	A549	lung:	n/a	chr1:169663577-169663585 chr1:169663572-169663590 chr1:169663567-169663588
17	CTCF	chr1:169663520-169663670	RPTEC	kidney:	n/a	chr1:169663577-169663585 chr1:169663572-169663590 chr1:169663567-169663588
18	CTCF	chr1:169663560-169663710	GM12873	blood:	n/a	chr1:169663577-169663585 chr1:169663572-169663590 chr1:169663567-169663588
19	CTCF	chr1:169669022-169669139	GM12878	blood:	n/a	n/a
20	CTCF	chr1:169669055-169669142	LNCaP	prostate:	n/a	n/a
21	CTCF	chr1:169663580-169663730	GM12865	blood:	n/a	n/a
22	CTCF	chr1:169663500-169663650	GM12866	blood:	n/a	chr1:169663577-169663585 chr1:169663572-169663590 chr1:169663567-169663588
23	CTCF	chr1:169669040-169669190	MCF-7	breast:	n/a	n/a
24	CTCF	chr1:169669120-169669270	GM06990	blood:	n/a	n/a
25	CTCF	chr1:169663520-169663670	GM12874	blood:	n/a	chr1:169663577-169663585 chr1:169663572-169663590 chr1:169663567-169663588
26	CTCF	chr1:169663620-169663770	GM12864	blood:	n/a	n/a
27	CTCF	chr1:169663570-169663627	K562	blood:	n/a	chr1:169663577-169663585 chr1:169663572-169663590
28	CTCF	chr1:169669122-169669176	GM12878	blood:	n/a	n/a
29	CTCF	chr1:169663470-169663675	H1-hESC	embryonic stem cell:	n/a	chr1:169663577-169663585 chr1:169663572-169663590 chr1:169663567-169663588
30	CTCF	chr1:169663540-169663690	MCF-7	breast:	n/a	chr1:169663577-169663585 chr1:169663572-169663590 chr1:169663567-169663588
31	CTCF	chr1:169663540-169663690	GM12865	blood:	n/a	chr1:169663577-169663585 chr1:169663572-169663590 chr1:169663567-169663588
32	CTCF	chr1:169663573-169663640	GM10266	blood:	n/a	chr1:169663577-169663585
33	CTCF	chr1:169663480-169663630	GM12872	blood:	n/a	chr1:169663577-169663585 chr1:169663572-169663590 chr1:169663567-169663588
34	CTCF	chr1:169668620-169668770	GM12874	blood:	n/a	n/a
35	CTCF	chr1:169663520-169663670	GM12869	blood:	n/a	chr1:169663577-169663585 chr1:169663572-169663590 chr1:169663567-169663588
36	CTCF	chr1:169663495-169663702	LNCaP	prostate:	n/a	chr1:169663577-169663585 chr1:169663572-169663590 chr1:169663567-169663588
37	CTCF	chr1:169663513-169663648	HUVEC	blood vessel:	n/a	chr1:169663577-169663585 chr1:169663572-169663590 chr1:169663567-169663588
38	CTCF	chr1:169668910-169669291	HCT-116	colon:	n/a	n/a
39	CTCF	chr1:169663540-169663690	HPAF	blood vessel:	n/a	chr1:169663577-169663585 chr1:169663572-169663590 chr1:169663567-169663588
40	CTCF	chr1:169663586-169663627	Lung_OC	lung:	n/a	n/a
41	CTCF	chr1:169663304-169663811	MCF-7	breast:	n/a	chr1:169663577-169663585 chr1:169663572-169663590 chr1:169663567-169663588
42	CTCF	chr1:169668978-169669282	MCF-7	breast:	n/a	n/a
43	CTCF	chr1:169669120-169669270	GM12873	blood:	n/a	n/a
44	CTCF	chr1:169663560-169663710	GM12872	blood:	n/a	chr1:169663577-169663585 chr1:169663572-169663590 chr1:169663567-169663588
45	CTCF	chr1:169669042-169669194	Hela-S3	cervix:	n/a	n/a
46	CTCF	chr1:169663540-169663690	GM12873	blood:	n/a	chr1:169663577-169663585 chr1:169663572-169663590 chr1:169663567-169663588
47	CTCF	chr1:169663400-169663690	GM12871	blood:	n/a	chr1:169663577-169663585 chr1:169663572-169663590 chr1:169663567-169663588
48	CTCF	chr1:169669060-169669210	MCF-7	breast:	n/a	n/a
49	CTCF	chr1:169663440-169663590	GM12878	blood:	n/a	chr1:169663577-169663585 chr1:169663572-169663590 chr1:169663567-169663588
50	CTCF	chr1:169669028-169669214	A549	lung:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:169671116-169671166	GM12878	blood:	n/a
2	chr1:169671116-169671166	AoSMC	blood vessel:	n/a
3	chr1:169671116-169671166	H1-hESC	embryonic stem cell:	embryo
4	chr1:169671116-169671166	HIPEpiC	eye:	n/a
5	chr1:169679199-169679249	U87	brain:	n/a
6	chr1:169671116-169671166	ovcar-3	ovarian:	n/a
7	chr1:169679199-169679249	HMEC	breast:	n/a
8	chr1:169679199-169679249	LNCaP	prostate:	n/a
9	chr1:169671116-169671166	NT2-D1	testis:	n/a
10	chr1:169679199-169679249	AG04449	skin:	fetal
11	chr1:169671116-169671166	SK-N-MC	brain:	n/a
12	chr1:169679199-169679249	NT2-D1	testis:	n/a
13	chr1:169679199-169679249	K562	blood:	n/a
14	chr1:169679199-169679249	HEK293	kidney:	embryo
15	chr1:169679199-169679249	CMK	blood:	n/a
16	chr1:169671116-169671166	AG04450	lung:	fetal
17	chr1:169671116-169671166	Hepatocyte	liver:	n/a
18	chr1:169679199-169679249	SKMC	muscle:	n/a
19	chr1:169671116-169671166	GM12891	blood:	n/a
20	chr1:169679199-169679249	HepG2	liver:	n/a
21	chr1:169671116-169671166	BJ	skin:	n/a
22	chr1:169679199-169679249	GM06990	blood:	n/a
23	chr1:169671116-169671166	HRPEpiC	eye:	n/a
24	chr1:169679199-169679249	HUVEC	blood vessel:	n/a
25	chr1:169679199-169679249	HIPEpiC	eye:	n/a
26	chr1:169671116-169671166	AG10803	skin:	n/a
27	chr1:169671116-169671166	HUVEC	blood vessel:	n/a
28	chr1:169679199-169679249	HPAEpiC	pulmonary alveolar:	n/a
29	chr1:169671116-169671166	HCM	heart:	n/a
30	chr1:169671116-169671166	GM06990	blood:	n/a
31	chr1:169671116-169671166	MCF-7	breast:	n/a
32	chr1:169679199-169679249	BE2_C	brain:	n/a
33	chr1:169671116-169671166	HCT-116	colon:	n/a
34	chr1:169679199-169679249	AG10803	skin:	n/a
35	chr1:169671116-169671166	SAEC	small airway:	n/a
36	chr1:169671116-169671166	HAEpiC	amniotic membrane:	n/a
37	chr1:169679199-169679249	HCPEpiC	choroid plexus:	n/a
38	chr1:169671116-169671166	HCF	heart:	n/a
39	chr1:169679199-169679249	GM12892	blood:	n/a
40	chr1:169671116-169671166	HRCEpiC	kidney:	n/a
41	chr1:169679199-169679249	NB4	blood:	n/a
42	chr1:169671116-169671166	GM19239	blood:	n/a
43	chr1:169679199-169679249	Hepatocyte	liver:	n/a
44	chr1:169679199-169679249	AG09319	gingival:	n/a
45	chr1:169671116-169671166	SKMC	muscle:	n/a
46	chr1:169671116-169671166	HNPCEpiC	eye:	n/a
47	chr1:169679199-169679249	GM12891	blood:	n/a
48	chr1:169679199-169679249	HRE	kidney:	n/a
49	chr1:169679199-169679249	GM19239	blood:	n/a
50	chr1:169679199-169679249	GM12878	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr1:169668678..169669639-chr1:169778642..169779434,3	MCF-7	breast:
2	chr1:169669179..169671320-chr1:169675894..169677671,2	K562	blood:
3	chr1:169570098..169571225-chr1:169663167..169664353,5	MCF-7	breast:
4	chr1:169674141..169677050-chr1:169763005..169764633,2	MCF-7	breast:
5	chr1:169669179..169671320-chr1:169675894..169677671,2	K562	blood:
6	chr1:169663115..169663861-chr1:169679931..169680901,2	MCF-7	breast:
7	chr1:169668675..169669722-chr1:169778297..169779287,4	MCF-7	breast:
8	chr1:169679878..169683283-chr1:169762041..169765464,5	MCF-7	breast:
9	chr1:169658516..169660936-chr1:169662078..169664299,2	K562	blood:
10	chr1:169519013..169520404-chr1:169662765..169663989,4	MCF-7	breast:
11	chr1:169555471..169556167-chr1:169663467..169664121,3	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SELE-1	chr1:169672396-169672470	NONHSAT007471
2	lnc-SELE-1	chr1:169665676-169665694	NONHSAT007471

Variant related genes	Relation type
SELL	TF binding region
SELL	CpG island
ENSG00000171806	chromatin interactions
ENSG00000198734	chromatin interactions
ENSG00000188404	chromatin interactions
ENSG00000000460	chromatin interactions

Extended variants
information (count: 757 )
Associated
traits (count: 92 )

Variant overlapped rSNPs/rCNVs (count:757 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4987379	chr1:169661299-169661300	Genic enhancers Enhancers Weak transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs186509542	chr1:169661300-169661301	Genic enhancers Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs4987378	chr1:169661333-169661334	Genic enhancers Enhancers Weak transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs372010449	chr1:169661346-169661347	Genic enhancers Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs112634318	chr1:169661353-169661354	Genic enhancers Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs369726645	chr1:169661366-169661367	Genic enhancers Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs201860477	chr1:169661383-169661384	Genic enhancers Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs67942205	chr1:169661384-169661385	Genic enhancers Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs386368682	chr1:169661385-169661386	Genic enhancers Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs60301674	chr1:169661387-169661388	Genic enhancers Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs138330083	chr1:169661388-169661389	Genic enhancers Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs372823788	chr1:169661389-169661390	Genic enhancers Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs148522917	chr1:169661390-169661391	Genic enhancers Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs376307984	chr1:169661391-169661392	Genic enhancers Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs12120772	chr1:169661393-169661394	Genic enhancers Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs58434075	chr1:169661394-169661395	Genic enhancers Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs577483998	chr1:169661436-169661437	Genic enhancers Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs191351185	chr1:169661437-169661438	Genic enhancers Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs139369009	chr1:169661452-169661453	Genic enhancers Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs572107464	chr1:169661453-169661454	Genic enhancers Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs542711802	chr1:169661474-169661475	Genic enhancers Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs4987405	chr1:169661489-169661490	Genic enhancers Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs4987377	chr1:169661500-169661501	Genic enhancers Enhancers Flanking Active TSS Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs4987376	chr1:169661501-169661502	Genic enhancers Enhancers Flanking Active TSS Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs113598168	chr1:169661542-169661543	Genic enhancers Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs4987375	chr1:169661555-169661556	Genic enhancers Enhancers Flanking Active TSS Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
27	rs4987374	chr1:169661639-169661640	Genic enhancers Enhancers Flanking Active TSS Weak transcription Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
28	rs559997545	chr1:169661640-169661641	Genic enhancers Enhancers Flanking Active TSS Weak transcription Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
29	rs188388429	chr1:169661645-169661646	Genic enhancers Enhancers Flanking Active TSS Weak transcription Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
30	rs549595938	chr1:169661657-169661658	Genic enhancers Enhancers Flanking Active TSS Weak transcription Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
31	rs548758412	chr1:169661730-169661731	Genic enhancers Enhancers Flanking Active TSS Weak transcription Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
32	rs192878961	chr1:169661911-169661912	Genic enhancers Enhancers Active TSS Flanking Active TSS Weak transcription Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
33	rs4987373	chr1:169661936-169661937	Genic enhancers Enhancers Active TSS Flanking Active TSS Weak transcription Transcr. at gene 5' and 3'	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs537535066	chr1:169661977-169661978	Genic enhancers Enhancers Active TSS Flanking Active TSS Weak transcription Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
35	rs538385075	chr1:169662026-169662027	Weak transcription Genic enhancers Flanking Active TSS Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs371655770	chr1:169662043-169662044	Weak transcription Genic enhancers Flanking Active TSS Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs552178117	chr1:169662078-169662079	Weak transcription Genic enhancers Flanking Active TSS Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs570482204	chr1:169662149-169662150	Weak transcription Genic enhancers Flanking Active TSS Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs538557836	chr1:169662214-169662215	Weak transcription Genic enhancers Flanking Active TSS Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs553605651	chr1:169662222-169662223	Weak transcription Genic enhancers Flanking Active TSS Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs185465951	chr1:169662230-169662231	Weak transcription Genic enhancers Flanking Active TSS Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs536100087	chr1:169662246-169662247	Weak transcription Genic enhancers Flanking Active TSS Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs371384008	chr1:169662277-169662278	Weak transcription Genic enhancers Flanking Active TSS Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs576085916	chr1:169662288-169662289	Weak transcription Genic enhancers Flanking Active TSS Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs551431904	chr1:169662308-169662309	Weak transcription Genic enhancers Flanking Active TSS Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs76182681	chr1:169662309-169662310	Weak transcription Genic enhancers Flanking Active TSS Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs571285932	chr1:169662311-169662312	Weak transcription Genic enhancers Flanking Active TSS Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs76349673	chr1:169662321-169662322	Weak transcription Genic enhancers Flanking Active TSS Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs74676253	chr1:169662322-169662323	Weak transcription Genic enhancers Flanking Active TSS Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs111305299	chr1:169662323-169662324	Weak transcription Genic enhancers Flanking Active TSS Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:92)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Autism	22495311	CNVD
Hepatocellular carcinoma	16750200	CNVD
Liposarcoma	21253554	CNVD
Burkitt''s lymphoma	18698080	CNVD
Melanoma	18172304	CNVD
Glioblastoma multiforme	21080181	CNVD
Cancer	21183584	CNVD
Multiple myeloma	16461302	CNVD
Rett syndrome	21593744	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Medulloblastoma	21979893	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
Bladder cancer	19088036	CNVD
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17002787	CNVD
Breast cancer	21858162	CNVD
Retinoblastoma	19183342	CNVD
Non-small cell lung cancer	21385341	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	16608533	CNVD
Ewing''s sarcoma	22429812	CNVD
Acute promyelocytic leukemia	19109227	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
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
Breast cancer	21611746	CNVD
Neuroblastoma	18923191	CNVD
Soft tissue tumor	16732325	CNVD
Cancer	17060936	CNVD
Lung cancer	16740712	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Ewing''s sarcoma	17952124	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Williams-beuren syndrome	16971481	CNVD
Developmental delay	21147756	CNVD
Burkitt''s lymphoma	20823134	CNVD
small cell lung cancer	20016488	CNVD
Myelofibrosis	22110671	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Lung cancer	18438408	CNVD
Cancer	20164920	CNVD

Chromatin state (count:440 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:169653200-169671600	Weak transcription	Spleen	Spleen
2	chr1:169656800-169662600	Enhancers	Primary T killer naive cells fromperipheralblood	blood
3	chr1:169657000-169661800	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
4	chr1:169658400-169666200	Enhancers	Thymus	Thymus
5	chr1:169659000-169661600	Genic enhancers	Primary B cells from peripheral blood	blood
6	chr1:169659200-169661400	Genic enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
7	chr1:169659600-169661800	Genic enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
8	chr1:169660000-169661400	Genic enhancers	Primary hematopoietic stem cells	blood
9	chr1:169660200-169661600	Genic enhancers	Monocytes-CD14+_RO01746	blood
10	chr1:169660400-169661800	Enhancers	Primary T helper naive cells fromperipheralblood	blood
11	chr1:169660400-169662800	Genic enhancers	Primary neutrophils fromperipheralblood	blood
12	chr1:169660600-169663600	Enhancers	Primary T helper cells fromperipheralblood	blood
13	chr1:169660600-169664000	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
14	chr1:169660800-169661400	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
15	chr1:169660800-169661800	Flanking Active TSS	Dnd41	blood
16	chr1:169660800-169662400	Enhancers	Primary T helper naive cells from peripheral blood	blood
17	chr1:169660800-169663000	Enhancers	Primary hematopoietic stem cells short term culture	blood
18	chr1:169660800-169664200	Enhancers	Primary T regulatory cells fromperipheralblood	blood
19	chr1:169660800-169665200	Genic enhancers	Primary monocytes fromperipheralblood	blood
20	chr1:169661000-169661600	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
21	chr1:169661200-169661400	Genic enhancers	Primary T cells from cord blood	blood
22	chr1:169661200-169661600	Enhancers	Primary T cells fromperipheralblood	blood
23	chr1:169661200-169661600	Enhancers	Primary T helper cells PMA-I stimulated	--
24	chr1:169661200-169661600	Enhancers	Primary T killer memory cells from peripheral blood	blood
25	chr1:169661200-169661600	Enhancers	GM12878-XiMat	blood
26	chr1:169661200-169662000	Enhancers	Primary B cells from cord blood	blood
27	chr1:169661200-169662400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
28	chr1:169661200-169663200	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
29	chr1:169661200-169664000	Enhancers	Fetal Thymus	thymus
30	chr1:169661200-169665400	Weak transcription	Sigmoid Colon	Sigmoid Colon
31	chr1:169661400-169661600	Enhancers	Primary T cells from cord blood	blood
32	chr1:169661400-169661600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
33	chr1:169661400-169662000	Flanking Active TSS	Primary T helper 17 cells PMA-I stimulated	--
34	chr1:169661400-169662400	Enhancers	Primary hematopoietic stem cells	blood
35	chr1:169661600-169661800	Flanking Active TSS	Primary T cells from cord blood	blood
36	chr1:169661600-169661800	Flanking Active TSS	Primary T cells fromperipheralblood	blood
37	chr1:169661600-169662000	Flanking Active TSS	Primary T helper memory cells from peripheral blood 2	blood
38	chr1:169661600-169662000	Flanking Active TSS	Primary T killer memory cells from peripheral blood	blood
39	chr1:169661600-169662000	Transcr. at gene 5' and 3'	Monocytes-CD14+_RO01746	blood
40	chr1:169661600-169662400	Enhancers	Primary B cells from peripheral blood	blood
41	chr1:169661600-169662800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
42	chr1:169661600-169663600	Flanking Active TSS	GM12878-XiMat	blood
43	chr1:169661600-169664000	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
44	chr1:169661800-169662200	Flanking Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
45	chr1:169661800-169662400	Active TSS	Primary T cells from cord blood	blood
46	chr1:169661800-169662400	Enhancers	Primary T cells fromperipheralblood	blood
47	chr1:169661800-169662400	Enhancers	Dnd41	blood
48	chr1:169661800-169663000	Flanking Active TSS	Primary T helper naive cells fromperipheralblood	blood
49	chr1:169661800-169663800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
50	chr1:169662000-169662400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood

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