Variant report

Variant	nsv160848
Chromosome Location	chr1:151789609-151796769
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	CEBPB	chr1:151792715-151793056	Hela-S3	cervix:	n/a	n/a
2	CTCF	chr1:151793700-151793850	Caco-2	colon:	n/a	n/a
3	E2F4	chr1:151792737-151792991	MCF10A-Er-Src	breast:	n/a	n/a
4	E2F6	chr1:151789920-151790265	H1-hESC	embryonic stem cell:	n/a	chr1:151790128-151790143 chr1:151790122-151790137
5	E2F6	chr1:151789842-151790332	H1-hESC	embryonic stem cell:	n/a	chr1:151790128-151790143 chr1:151790122-151790137
6	EGR1	chr1:151794831-151795173	K562	blood:	n/a	chr1:151795011-151795021
7	EGR1	chr1:151794871-151795093	K562	blood:	n/a	chr1:151795011-151795021
8	EGR1	chr1:151794935-151795097	GM12878	blood:	n/a	chr1:151795011-151795021
9	ELK1	chr1:151792788-151793027	Hela-S3	cervix:	n/a	n/a
10	ELK4	chr1:151792775-151793046	Hela-S3	cervix:	n/a	n/a
11	EP300	chr1:151794775-151796209	SK-N-SH	brain:	n/a	n/a
12	EP300	chr1:151792647-151794532	SK-N-SH	brain:	n/a	chr1:151793475-151793489 chr1:151793708-151793722
13	EP300	chr1:151792782-151792988	Hela-S3	cervix:	n/a	n/a
14	EP300	chr1:151793401-151793790	SK-N-SH_RA	brain:	n/a	chr1:151793475-151793489 chr1:151793708-151793722
15	EP300	chr1:151793372-151793872	SK-N-SH_RA	brain:	n/a	chr1:151793475-151793489 chr1:151793708-151793722
16	FOS	chr1:151789530-151789702	MCF10A-Er-Src	breast:	n/a	chr1:151789662-151789669
17	FOS	chr1:151792682-151793075	MCF10A-Er-Src	breast:	n/a	n/a
18	FOS	chr1:151789571-151789744	MCF10A-Er-Src	breast:	n/a	chr1:151789662-151789669
19	FOS	chr1:151792702-151793102	MCF10A-Er-Src	breast:	n/a	n/a
20	FOS	chr1:151789556-151789768	MCF10A-Er-Src	breast:	n/a	chr1:151789662-151789669
21	FOS	chr1:151792679-151793063	MCF10A-Er-Src	breast:	n/a	n/a
22	FOS	chr1:151789527-151789764	MCF10A-Er-Src	breast:	n/a	chr1:151789662-151789669
23	FOS	chr1:151792725-151793055	MCF10A-Er-Src	breast:	n/a	n/a
24	GATA2	chr1:151793232-151794451	SH-SY5Y	brain:	n/a	chr1:151793893-151793904
25	GATA3	chr1:151794316-151794358	SH-SY5Y	brain:	n/a	n/a
26	GATA3	chr1:151793312-151793975	SK-N-SH	brain:	n/a	chr1:151793893-151793904
27	GATA3	chr1:151793382-151793902	SK-N-SH	brain:	n/a	n/a
28	GATA3	chr1:151793224-151794002	SH-SY5Y	brain:	n/a	chr1:151793893-151793904
29	GTF2F1	chr1:151792835-151792949	Hela-S3	cervix:	n/a	n/a
30	JUND	chr1:151789513-151789660	K562	blood:	n/a	n/a
31	MAX	chr1:151792773-151793005	Hela-S3	cervix:	n/a	chr1:151792896-151792905
32	MAX	chr1:151789864-151790103	NB4	blood:	n/a	n/a
33	MAZ	chr1:151792823-151792992	Hela-S3	cervix:	n/a	chr1:151792896-151792905
34	MXI1	chr1:151794905-151796121	SK-N-SH	brain:	n/a	n/a
35	MYC	chr1:151789626-151789638	MCF10A-Er-Src	breast:	n/a	n/a
36	MYC	chr1:151792733-151793054	MCF10A-Er-Src	breast:	n/a	chr1:151792896-151792905
37	MYC	chr1:151792757-151793055	MCF10A-Er-Src	breast:	n/a	chr1:151792896-151792905
38	NFIC	chr1:151793290-151793936	SK-N-SH	brain:	n/a	chr1:151793647-151793675
39	NFIC	chr1:151793366-151793853	SK-N-SH	brain:	n/a	chr1:151793647-151793675
40	NFIC	chr1:151793534-151793869	ECC-1	luminal epithelium:	n/a	chr1:151793647-151793675
41	PBX3	chr1:151793483-151793869	SK-N-SH	brain:	n/a	n/a
42	POLR2A	chr1:151789323-151789737	H1-neurons	neurons:	n/a	n/a
43	POLR2A	chr1:151793452-151793786	SK-N-SH	brain:	n/a	n/a
44	POLR2A	chr1:151793487-151793745	SK-N-SH	brain:	n/a	n/a
45	POLR2A	chr1:151789433-151789739	H1-neurons	neurons:	n/a	n/a
46	RAD21	chr1:151793410-151793806	SK-N-SH_RA	brain:	n/a	n/a
47	RAD21	chr1:151793451-151793732	SK-N-SH_RA	brain:	n/a	n/a
48	RAD21	chr1:151792837-151792932	Hela-S3	cervix:	n/a	n/a
49	REST	chr1:151793501-151793790	SK-N-SH	brain:	n/a	chr1:151793682-151793691
50	REST	chr1:151793438-151793844	PFSK-1	brain:	n/a	chr1:151793682-151793691

No.	Distal block	Cell Line	Cell type
1	chr1:151729177..151730822-chr1:151791781..151793966,2	MCF-7	breast:
2	chr1:151786405..151788283-chr1:151795067..151797465,2	MCF-7	breast:
3	chr1:151763352..151764892-chr1:151792171..151794481,2	MCF-7	breast:
4	chr1:151782043..151784964-chr1:151791094..151793186,2	K562	blood:
5	chr1:151761172..151762786-chr1:151788164..151789988,2	MCF-7	breast:
6	chr1:151768081..151769884-chr1:151790238..151792555,2	MCF-7	breast:
7	chr1:151749151..151752129-chr1:151789791..151791884,2	MCF-7	breast:
8	chr1:151789315..151792282-chr1:151793123..151796667,3	MCF-7	breast:
9	chr1:151779245..151781251-chr1:151789971..151792071,2	K562	blood:
10	chr1:151782377..151784450-chr1:151790300..151792878,2	MCF-7	breast:
11	chr1:151734599..151737302-chr1:151792867..151794521,3	MCF-7	breast:
12	chr1:151788480..151790038-chr1:151792565..151794088,2	K562	blood:
13	chr1:151789925..151792025-chr1:151796878..151798485,2	K562	blood:
14	chr1:151789798..151791316-chr1:151791321..151793300,2	MCF-7	breast:
15	chr1:151795588..151797929-chr1:151801830..151803659,3	MCF-7	breast:
16	chr1:151732397..151736165-chr1:151791391..151794287,3	MCF-7	breast:
17	chr1:151786877..151789980-chr1:151790963..151794065,3	K562	blood:
18	chr1:151795525..151798477-chr1:151809091..151811611,2	MCF-7	breast:
19	chr1:151777634..151779857-chr1:151790173..151792393,2	MCF-7	breast:
20	chr1:151789315..151792282-chr1:151793123..151796667,3	MCF-7	breast:
21	chr1:151778487..151781437-chr1:151789485..151791157,2	K562	blood:
22	chr1:151789798..151791316-chr1:151791321..151793300,2	MCF-7	breast:
23	chr1:151795791..151798042-chr1:151801058..151802708,2	K562	blood:
24	chr1:151785706..151787587-chr1:151791618..151793620,2	MCF-7	breast:
25	chr1:151791300..151792118-chr18:74203868..74204679,2	HCT-116	colon:
26	chr1:151788480..151790038-chr1:151792565..151794088,2	K562	blood:
27	chr1:151762692..151764712-chr1:151794747..151796682,2	MCF-7	breast:
28	chr1:151789037..151791366-chr1:151802324..151804335,2	K562	blood:

Variant related genes	Relation type
RORC	TF binding region
ENSG00000213171	chromatin interactions
ENSG00000143365	chromatin interactions
ENSG00000203288	chromatin interactions
ENSG00000143450	chromatin interactions
ENSG00000236940	chromatin interactions
ENSG00000182134	chromatin interactions
ENSG00000143436	chromatin interactions

Extended variants
information (count: 263 )
Associated
traits (count: 117 )

Variant overlapped rSNPs/rCNVs (count:263 , 50 per page) page: 1 2 3 4 5 6

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs56273334	chr1:151789609-151789610	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
2	rs55841824	chr1:151789611-151789612	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs566041533	chr1:151789614-151789615	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs534955391	chr1:151789616-151789617	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs555168862	chr1:151789617-151789618	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs373945888	chr1:151789618-151789619	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs543540722	chr1:151789619-151789620	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs201459328	chr1:151789626-151789627	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs373236748	chr1:151789635-151789636	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs12144914	chr1:151789647-151789648	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs200661181	chr1:151789677-151789678	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs201387188	chr1:151789683-151789684	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs199749252	chr1:151789689-151789690	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs200606878	chr1:151789698-151789699	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs201478663	chr1:151789713-151789714	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs199920990	chr1:151789722-151789723	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs200735068	chr1:151789767-151789768	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs201827125	chr1:151789785-151789786	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs200049152	chr1:151789790-151789791	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs201029150	chr1:151789796-151789797	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs116467908	chr1:151789853-151789854	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs139073303	chr1:151789860-151789861	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs181577636	chr1:151789885-151789886	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs184719416	chr1:151789904-151789905	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs188606497	chr1:151789963-151789964	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs149883588	chr1:151789975-151789976	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs35557851	chr1:151789985-151789986	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs113229369	chr1:151789990-151789991	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs141952961	chr1:151790022-151790023	Weak transcription Strong transcription Enhancers Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs181426583	chr1:151790051-151790052	Weak transcription Strong transcription Enhancers Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs185831412	chr1:151790067-151790068	Weak transcription Strong transcription Enhancers Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs150688114	chr1:151790068-151790069	Weak transcription Strong transcription Enhancers Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs535015867	chr1:151790080-151790081	Weak transcription Strong transcription Enhancers Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs554951404	chr1:151790086-151790087	Weak transcription Strong transcription Enhancers Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs571842602	chr1:151790133-151790134	Weak transcription Strong transcription Enhancers Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs34914274	chr1:151790142-151790143	Weak transcription Strong transcription Enhancers Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs537243753	chr1:151790150-151790151	Weak transcription Strong transcription Enhancers Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs564125987	chr1:151790201-151790202	Weak transcription Strong transcription Enhancers Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs191033234	chr1:151790234-151790235	Weak transcription Strong transcription Enhancers Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs73009617	chr1:151790251-151790252	Weak transcription Strong transcription Enhancers Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs558056333	chr1:151790263-151790264	Weak transcription Strong transcription Enhancers Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs375608634	chr1:151790267-151790268	Weak transcription Strong transcription Enhancers Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs545876891	chr1:151790273-151790274	Weak transcription Strong transcription Enhancers Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs7540027	chr1:151790311-151790312	Weak transcription Strong transcription Enhancers Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs7540034	chr1:151790339-151790340	Weak transcription Strong transcription Enhancers Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs542141591	chr1:151790364-151790365	Weak transcription Strong transcription Enhancers Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs34818694	chr1:151790374-151790375	Weak transcription Strong transcription Enhancers Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs61815118	chr1:151790383-151790384	Weak transcription Strong transcription Enhancers Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs575450752	chr1:151790435-151790436	Weak transcription Strong transcription Enhancers Transcr. at gene 5' and 3' Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs79469888	chr1:151790511-151790512	Weak transcription Strong transcription Enhancers Transcr. at gene 5' and 3' Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:117)

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
Cancer	21129771	CNVD
Non-small cell lung cancer	21385341	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
Ewing''s sarcoma	21437220	CNVD
Liposarcoma	21253554	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	18698080	CNVD
Melanoma	18172304	CNVD
Breast cancer	20409316	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17393978	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
Acute lymphoblastic leukemia	17443227	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	CNVD
Esophageal squamous carcinoma	18350619	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
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
Breast cancer	21611746	CNVD
Retinoblastoma	19183342	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	16608533	CNVD
Ewing''s sarcoma	22429812	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Ewing''s sarcoma	17952124	CNVD
Osteosarcoma	17242211	CNVD
Ovarian cancer	17242211	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Schizophrenia	18990708	CNVD
Sudden cardiac death	19188705	CNVD
Plasma-cell dyscrasia	16705089	CNVD
Myeloma	17024118	CNVD
Cancer	17060936	CNVD
Multiple myeloma	16616336	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
Follicular lymphoma	18703704	CNVD
Breast cancer	21509527	CNVD
Bladder cancer	21909424	CNVD
Acute myeloid leukemia	20729466	CNVD
Hodgkin''s lymphoma	17606441	CNVD
small cell lung cancer	20016488	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Myelofibrosis	22110671	CNVD
Liver carcinoma	19366792	CNVD
Testicular germ cell tumor	18059402	CNVD
Trisomy 5 syndrome	21098271	CNVD
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
Gastrointestinal cancer	16790693	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Glioblastoma multiforme	21138945	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:257 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:151764200-151792800	Weak transcription	Lung	lung
2	chr1:151778400-151792800	Weak transcription	Left Ventricle	heart
3	chr1:151778600-151792000	Strong transcription	Breast Myoepithelial Primary Cells	Breast
4	chr1:151778600-151802400	Weak transcription	Pancreatic Islets	Pancreatic Islet
5	chr1:151780000-151793400	Weak transcription	Stomach Mucosa	stomach
6	chr1:151782000-151791000	Weak transcription	Sigmoid Colon	Sigmoid Colon
7	chr1:151782800-151790400	Strong transcription	Skeletal Muscle Male	skeletal muscle
8	chr1:151783600-151790800	Strong transcription	Pancreas	Pancrea
9	chr1:151783600-151791400	Weak transcription	Hela-S3	cervix
10	chr1:151783800-151792000	Weak transcription	Psoas Muscle	Psoas
11	chr1:151784400-151789800	Strong transcription	Skeletal Muscle Female	skeletal muscle
12	chr1:151784800-151794600	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
13	chr1:151784800-151794800	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
14	chr1:151786600-151791000	Strong transcription	Rectal Mucosa Donor 29	rectum
15	chr1:151786600-151793600	Enhancers	Primary T helper cells PMA-I stimulated	--
16	chr1:151786800-151793600	Enhancers	Primary T helper cells fromperipheralblood	blood
17	chr1:151786800-151795000	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
18	chr1:151787000-151790600	Enhancers	Primary hematopoietic stem cells short term culture	blood
19	chr1:151787000-151791600	Enhancers	Fetal Muscle Leg	muscle
20	chr1:151787200-151790400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
21	chr1:151787200-151790800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
22	chr1:151787400-151800000	Weak transcription	Spleen	Spleen
23	chr1:151787600-151790200	Enhancers	Primary T cells from cord blood	blood
24	chr1:151787600-151791000	Enhancers	Primary hematopoietic stem cells	blood
25	chr1:151788200-151789800	Weak transcription	Primary B cells from peripheral blood	blood
26	chr1:151788200-151793200	Transcr. at gene 5' and 3'	Thymus	Thymus
27	chr1:151788200-151796800	Transcr. at gene 5' and 3'	Fetal Thymus	thymus
28	chr1:151788600-151790000	Enhancers	Fetal Muscle Trunk	muscle
29	chr1:151788800-151790600	Enhancers	Primary T regulatory cells fromperipheralblood	blood
30	chr1:151788800-151792200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
31	chr1:151789000-151790000	Enhancers	Primary T killer naive cells fromperipheralblood	blood
32	chr1:151789000-151790200	Enhancers	Fetal Intestine Large	intestine
33	chr1:151789000-151790400	Enhancers	Primary T killer memory cells from peripheral blood	blood
34	chr1:151789000-151791000	Enhancers	Esophagus	oesophagus
35	chr1:151789000-151792000	Weak transcription	Rectal Mucosa Donor 31	rectum
36	chr1:151789000-151792400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
37	chr1:151789000-151793000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
38	chr1:151789200-151790000	Genic enhancers	Primary T helper 17 cells PMA-I stimulated	--
39	chr1:151789200-151790000	Enhancers	Fetal Intestine Small	intestine
40	chr1:151789200-151790200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
41	chr1:151789200-151790200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
42	chr1:151789200-151790200	Genic enhancers	Duodenum Mucosa	Duodenum
43	chr1:151789400-151790200	Enhancers	NHEK	skin
44	chr1:151789400-151790600	Flanking Active TSS	Dnd41	blood
45	chr1:151789400-151791600	Genic enhancers	Liver	Liver
46	chr1:151789400-151794400	Enhancers	Primary T cells fromperipheralblood	blood
47	chr1:151789400-151794600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
48	chr1:151789600-151790000	Enhancers	Monocytes-CD14+_RO01746	blood
49	chr1:151789600-151790400	Enhancers	Primary monocytes fromperipheralblood	blood
50	chr1:151789600-151792000	Weak transcription	Gastric	stomach

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