Variant report

Variant	nsv872492
Chromosome Location	chr1:161009523-161013152
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:259)
CpG islands
(count:244)
Chromatin interactive
region (count:18)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:259 , 50 per page) page: 1 2 3 4 5 6

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BHLHE40	chr1:161011288-161011608	K562	blood:	n/a	n/a
2	BHLHE40	chr1:161011384-161011490	GM12878	blood:	n/a	n/a
3	CEBPB	chr1:161011375-161011561	Hela-S3	cervix:	n/a	n/a
4	CEBPB	chr1:161011430-161011537	K562	blood:	n/a	n/a
5	CEBPB	chr1:161011362-161011436	HepG2	liver:	n/a	n/a
6	CHD2	chr1:161011400-161011588	GM12878	blood:	n/a	n/a
7	CTCF	chr1:161011320-161011470	AG09319	gingival:	n/a	n/a
8	CTCF	chr1:161011330-161011558	LNCaP	prostate:	n/a	n/a
9	CTCF	chr1:161011316-161011576	MCF-7	breast:	n/a	n/a
10	CTCF	chr1:161011340-161011490	BE2_C	brain:	n/a	n/a
11	CTCF	chr1:161011272-161011572	Spleen_OC	spleen:	n/a	n/a
12	CTCF	chr1:161011380-161011530	HepG2	liver:	n/a	n/a
13	CTCF	chr1:161011940-161012090	GM12864	blood:	n/a	n/a
14	CTCF	chr1:161011080-161011230	GM12875	blood:	n/a	n/a
15	CTCF	chr1:161011360-161011510	HEK293	kidney:	n/a	n/a
16	CTCF	chr1:161011297-161011617	NHEK	skin:	n/a	n/a
17	CTCF	chr1:161010960-161011110	AG09319	gingival:	n/a	n/a
18	CTCF	chr1:161011360-161011510	SAEC	small airway:	n/a	n/a
19	CTCF	chr1:161011322-161011593	MCF-7	breast:	n/a	n/a
20	CTCF	chr1:161011302-161011610	Gliobla	brain:	n/a	n/a
21	CTCF	chr1:161011360-161011510	K562	blood:	n/a	n/a
22	CTCF	chr1:161011880-161012030	BJ	skin:	n/a	n/a
23	CTCF	chr1:161011322-161011601	MCF-7	breast:	n/a	n/a
24	CTCF	chr1:161011346-161011543	SK-N-SH_RA	brain:	n/a	n/a
25	CTCF	chr1:161011360-161011510	NHDF-neo	bronchial:	n/a	n/a
26	CTCF	chr1:161011360-161011510	Hela-S3	cervix:	n/a	n/a
27	CTCF	chr1:161011340-161011490	RPTEC	kidney:	n/a	n/a
28	CTCF	chr1:161011360-161011510	AG04450	lung:	n/a	n/a
29	CTCF	chr1:161013120-161013270	A549	lung:	n/a	n/a
30	CTCF	chr1:161011400-161011550	GM06990	blood:	n/a	n/a
31	CTCF	chr1:161011360-161011510	GM12864	blood:	n/a	n/a
32	CTCF	chr1:161011360-161011510	SK-N-SH_RA	brain:	n/a	n/a
33	CTCF	chr1:161011304-161011546	HepG2	liver:	n/a	n/a
34	CTCF	chr1:161011303-161011616	GM19239	blood:	n/a	n/a
35	CTCF	chr1:161011336-161011555	GM20000	blood:	n/a	n/a
36	CTCF	chr1:161011380-161011530	AoAF	blood vessel:	n/a	n/a
37	CTCF	chr1:161011261-161011649	IMR90	lung:	n/a	n/a
38	CTCF	chr1:161011347-161011571	A549	lung:	n/a	n/a
39	CTCF	chr1:161011340-161011490	HFF	foreskin:	n/a	n/a
40	CTCF	chr1:161011340-161011490	GM12869	blood:	n/a	n/a
41	CTCF	chr1:161011380-161011530	GM12878	blood:	n/a	n/a
42	CTCF	chr1:161011338-161011541	Pancreas_OC	pancreas:	n/a	n/a
43	CTCF	chr1:161011332-161011575	GM10248	blood:	n/a	n/a
44	CTCF	chr1:161011320-161011470	HMEC	breast:	n/a	n/a
45	CTCF	chr1:161011360-161011510	AG10803	skin:	n/a	n/a
46	CTCF	chr1:161011320-161011470	WI-38	lung:	n/a	n/a
47	CTCF	chr1:161011400-161011550	HRE	kidney:	n/a	n/a
48	CTCF	chr1:161011360-161011510	GM12873	blood:	n/a	n/a
49	CTCF	chr1:161011380-161011530	HRE	kidney:	n/a	n/a
50	CTCF	chr1:161011324-161011568	GM13977	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	chr1:161010071-161010121	AG04449	skin:	fetal
2	chr1:161009753-161009803	NH-A	brain:	n/a
3	chr1:161009644-161009694	HMEC	breast:	n/a
4	chr1:161010071-161010121	HepG2	liver:	n/a
5	chr1:161009753-161009803	HUVEC	blood vessel:	n/a
6	chr1:161009753-161009803	HRCEpiC	kidney:	n/a
7	chr1:161009753-161009803	Hepatocyte	liver:	n/a
8	chr1:161009644-161009694	PrEC	prostate:	n/a
9	chr1:161010071-161010121	H1-hESC	embryonic stem cell:	embryo
10	chr1:161010071-161010121	Caco-2	colon:	n/a
11	chr1:161009753-161009803	HCF	heart:	n/a
12	chr1:161010071-161010121	NHDF-neo	bronchial:	n/a
13	chr1:161011634-161011684	ovcar-3	ovarian:	n/a
14	chr1:161011634-161011684	HRE	kidney:	n/a
15	chr1:161009753-161009803	PFSK-1	brain:	n/a
16	chr1:161009644-161009694	ProgFib	skin:	n/a
17	chr1:161009644-161009694	HRCEpiC	kidney:	n/a
18	chr1:161009753-161009803	H1-hESC	embryonic stem cell:	embryo
19	chr1:161009753-161009803	GM19239	blood:	n/a
20	chr1:161009644-161009694	Hela-S3	cervix:	n/a
21	chr1:161011634-161011684	MCF-7	breast:	n/a
22	chr1:161011634-161011684	AoSMC	blood vessel:	n/a
23	chr1:161009753-161009803	SAEC	small airway:	n/a
24	chr1:161011634-161011684	HAEpiC	amniotic membrane:	n/a
25	chr1:161011634-161011684	SK-N-MC	brain:	n/a
26	chr1:161011634-161011684	NT2-D1	testis:	n/a
27	chr1:161010071-161010121	HCT-116	colon:	n/a
28	chr1:161011634-161011684	AG04450	lung:	fetal
29	chr1:161010071-161010121	GM12891	blood:	n/a
30	chr1:161011634-161011684	HPAEpiC	pulmonary alveolar:	n/a
31	chr1:161009644-161009694	GM12878	blood:	n/a
32	chr1:161009644-161009694	RPTEC	kidney:	n/a
33	chr1:161009644-161009694	HNPCEpiC	eye:	n/a
34	chr1:161009644-161009694	NHDF-neo	bronchial:	n/a
35	chr1:161010071-161010121	SKMC	muscle:	n/a
36	chr1:161011634-161011684	PrEC	prostate:	n/a
37	chr1:161011634-161011684	SK-N-SH	brain:	n/a
38	chr1:161009753-161009803	HAEpiC	amniotic membrane:	n/a
39	chr1:161009644-161009694	GM12891	blood:	n/a
40	chr1:161011634-161011684	Caco-2	colon:	n/a
41	chr1:161010071-161010121	AG09319	gingival:	n/a
42	chr1:161010071-161010121	Jurkat	blood:	n/a
43	chr1:161010071-161010121	U87	brain:	n/a
44	chr1:161011634-161011684	Hepatocyte	liver:	n/a
45	chr1:161010071-161010121	HL-60	blood:	n/a
46	chr1:161011634-161011684	Hela-S3	cervix:	n/a
47	chr1:161009753-161009803	Caco-2	colon:	n/a
48	chr1:161009644-161009694	AG04449	skin:	fetal
49	chr1:161010071-161010121	LNCaP	prostate:	n/a
50	chr1:161009753-161009803	NT2-D1	testis:	n/a

(count:18 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:160989663..160992818-chr1:161011844..161017868,15	MCF-7	breast:
2	chr1:160988819..160994033-chr1:161005548..161011188,8	MCF-7	breast:
3	chr1:161012196..161017661-chr1:161066183..161070852,8	MCF-7	breast:
4	chr1:161006846..161009787-chr1:161123441..161125743,2	MCF-7	breast:
5	chr1:161011414..161013032-chr1:161129851..161132212,2	K562	blood:
6	chr1:161011228..161012764-chr1:161122593..161124625,2	K562	blood:
7	chr1:161012288..161019472-chr1:161047717..161055328,13	MCF-7	breast:
8	chr1:161011663..161014033-chr1:161014079..161015803,2	K562	blood:
9	chr1:161006354..161009878-chr1:161042497..161045575,4	MCF-7	breast:
10	chr1:161007064..161010778-chr1:161101040..161104167,3	MCF-7	breast:
11	chr1:160989495..160995605-chr1:161004888..161010340,15	MCF-7	breast:
12	chr1:160988071..160992174-chr1:161007125..161014242,7	K562	blood:
13	chr1:161007165..161010190-chr1:161058502..161060475,3	MCF-7	breast:
14	chr1:161007801..161009697-chr1:161067796..161070375,2	K562	blood:
15	chr1:161005808..161012985-chr1:161064732..161070101,9	MCF-7	breast:
16	chr1:160988929..160992185-chr1:161012707..161018170,8	MCF-7	breast:
17	chr1:161007047..161009717-chr1:161100084..161102311,2	K562	blood:
18	chr1:160989087..160991942-chr1:161007144..161014242,6	K562	blood:

No data

Variant related genes	Relation type
ENSG00000270149	TF binding region
TSTD1	TF binding region
USF1	TF binding region
ENSG00000270149	CpG island
TSTD1	CpG island
USF1	CpG island
ENSG00000158773	chromatin interactions
ENSG00000158796	chromatin interactions
ENSG00000143217	chromatin interactions
ENSG00000143222	chromatin interactions
ENSG00000143258	chromatin interactions
ENSG00000162755	chromatin interactions
ENSG00000228917	chromatin interactions
ENSG00000158769	chromatin interactions

Extended variants
information (count: 166 )
Associated
traits (count: 114 )

Variant overlapped rSNPs/rCNVs (count:166 , 50 per page) page: 1 2 3 4

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs3737787	chr1:161009523-161009524	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region Chromatin interactive region	7 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs34985495	chr1:161009547-161009548	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
3	rs563337826	chr1:161009556-161009557	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
4	rs79449582	chr1:161009617-161009618	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
5	rs185784991	chr1:161009645-161009646	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
6	rs17181932	chr1:161009680-161009681	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	7 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs200506802	chr1:161009706-161009707	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
8	rs367551534	chr1:161009717-161009718	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
9	rs200060439	chr1:161009723-161009724	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
10	rs146372368	chr1:161009746-161009747	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
11	rs61559246	chr1:161009779-161009780	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
12	rs372202871	chr1:161009847-161009848	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
13	rs375230019	chr1:161009850-161009851	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
14	rs34768851	chr1:161009886-161009887	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
15	rs12072782	chr1:161009890-161009891	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
16	rs571476872	chr1:161009941-161009942	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
17	rs35366711	chr1:161009954-161009955	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
18	rs368456852	chr1:161009966-161009967	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
19	rs141478104	chr1:161010019-161010020	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
20	rs369815605	chr1:161010195-161010196	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs536819727	chr1:161010202-161010203	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs550376620	chr1:161010270-161010271	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
23	rs17215359	chr1:161010283-161010284	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
24	rs17175540	chr1:161010305-161010306	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs553237947	chr1:161010306-161010307	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
26	rs201864171	chr1:161010356-161010357	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
27	rs368917798	chr1:161010358-161010359	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
28	rs372940280	chr1:161010359-161010360	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
29	rs372068185	chr1:161010363-161010364	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
30	rs369207174	chr1:161010396-161010397	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
31	rs138288820	chr1:161010423-161010424	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
32	rs112811086	chr1:161010442-161010443	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
33	rs374446474	chr1:161010452-161010453	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
34	rs377459002	chr1:161010485-161010486	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
35	rs370235301	chr1:161010502-161010503	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
36	rs375339608	chr1:161010503-161010504	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
37	rs141965906	chr1:161010535-161010536	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
38	rs370847325	chr1:161010552-161010553	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
39	rs368066674	chr1:161010646-161010647	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
40	rs368360944	chr1:161010667-161010668	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
41	rs375380563	chr1:161010690-161010691	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
42	rs561471631	chr1:161010703-161010704	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
43	rs575135490	chr1:161010711-161010712	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
44	rs2073658	chr1:161010762-161010763	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
45	rs2516841	chr1:161010774-161010775	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
46	rs17175519	chr1:161010776-161010777	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs35841490	chr1:161010789-161010790	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs564800547	chr1:161010790-161010791	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs2073657	chr1:161010791-161010792	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
50	rs550313303	chr1:161010827-161010828	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:114)

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
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

Chromatin state (count:299 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:161007000-161013400	Strong transcription	Cortex derived primary cultured neurospheres	brain
2	chr1:161007400-161013400	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
3	chr1:161007400-161013400	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
4	chr1:161007400-161013400	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
5	chr1:161007400-161013400	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
6	chr1:161007600-161013400	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
7	chr1:161008000-161013200	Strong transcription	A549	lung
8	chr1:161008000-161013400	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
9	chr1:161008200-161013000	Strong transcription	NHLF	lung
10	chr1:161008600-161009600	Genic enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
11	chr1:161008600-161009800	Weak transcription	Fetal Heart	heart
12	chr1:161008600-161011400	Strong transcription	Foreskin Fibroblast Primary Cells skin02	Skin
13	chr1:161008800-161012600	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
14	chr1:161008800-161013000	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
15	chr1:161008800-161013400	Strong transcription	Brain Cingulate Gyrus	brain
16	chr1:161008800-161014000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
17	chr1:161009000-161009600	Genic enhancers	ES-UCSF4 Cell Line	embryonic stem cell
18	chr1:161009000-161009600	Genic enhancers	Primary neutrophils fromperipheralblood	blood
19	chr1:161009000-161009600	Genic enhancers	Placenta	Placenta
20	chr1:161009000-161009600	Genic enhancers	HSMM	muscle
21	chr1:161009000-161009600	Genic enhancers	Monocytes-CD14+_RO01746	blood
22	chr1:161009000-161009800	Genic enhancers	Primary hematopoietic stem cells short term culture	blood
23	chr1:161009000-161009800	Genic enhancers	Primary Natural Killer cells fromperipheralblood	blood
24	chr1:161009000-161009800	Genic enhancers	Skeletal Muscle Female	skeletal muscle
25	chr1:161009000-161010000	Genic enhancers	Colonic Mucosa	Colon
26	chr1:161009000-161010000	Weak transcription	Pancreatic Islets	Pancreatic Islet
27	chr1:161009000-161010000	Genic enhancers	Fetal Muscle Leg	muscle
28	chr1:161009000-161010000	Genic enhancers	Fetal Thymus	thymus
29	chr1:161009000-161010000	Weak transcription	Ovary	ovary
30	chr1:161009000-161010400	Genic enhancers	Spleen	Spleen
31	chr1:161009000-161011800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
32	chr1:161009000-161012400	Weak transcription	Psoas Muscle	Psoas
33	chr1:161009000-161012600	Strong transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
34	chr1:161009000-161012800	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
35	chr1:161009000-161012800	Strong transcription	Adipose Nuclei	Adipose
36	chr1:161009000-161013200	Strong transcription	Osteobl	bone
37	chr1:161009000-161013400	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
38	chr1:161009000-161013400	Strong transcription	Fetal Stomach	stomach
39	chr1:161009000-161014000	Genic enhancers	Primary B cells from peripheral blood	blood
40	chr1:161009200-161009600	Genic enhancers	H1 Cell Line	embryonic stem cell
41	chr1:161009200-161009600	Genic enhancers	Breast Myoepithelial Primary Cells	Breast
42	chr1:161009200-161009600	Transcr. at gene 5' and 3'	Primary T helper naive cells from peripheral blood	blood
43	chr1:161009200-161009600	Genic enhancers	Primary T regulatory cells fromperipheralblood	blood
44	chr1:161009200-161009600	Transcr. at gene 5' and 3'	Primary hematopoietic stem cells G-CSF-mobilized Male	--
45	chr1:161009200-161009600	Transcr. at gene 5' and 3'	Foreskin Keratinocyte Primary Cells skin02	Skin
46	chr1:161009200-161009600	Transcr. at gene 5' and 3'	Liver	Liver
47	chr1:161009200-161009600	Genic enhancers	Brain Germinal Matrix	brain
48	chr1:161009200-161009600	Genic enhancers	Fetal Intestine Large	intestine
49	chr1:161009200-161009600	Genic enhancers	Fetal Intestine Small	intestine
50	chr1:161009200-161009600	Genic enhancers	Fetal Muscle Trunk	muscle

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