Variant report

Variant	esv3441716
Chromosome Location	chr1:179197554-179200302
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	ARID3A	chr1:179199136-179200040	K562	blood:	n/a	n/a
2	BACH1	chr1:179199014-179199144	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr1:179197999-179198219	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr1:179199309-179199782	K562	blood:	n/a	n/a
5	BATF	chr1:179197567-179197815	GM12878	blood:	n/a	n/a
6	BHLHE40	chr1:179199120-179199730	K562	blood:	n/a	n/a
7	BRCA1	chr1:179198569-179198595	Hela-S3	cervix:	n/a	n/a
8	CCNT2	chr1:179198363-179198791	K562	blood:	n/a	n/a
9	CCNT2	chr1:179199028-179199235	K562	blood:	n/a	n/a
10	CEBPB	chr1:179197798-179198105	IMR90	lung:	n/a	chr1:179197958-179197971
11	CEBPB	chr1:179197781-179198224	Hela-S3	cervix:	n/a	chr1:179197958-179197971
12	CEBPD	chr1:179198561-179198954	HepG2	liver:	n/a	n/a
13	CHD1	chr1:179198389-179198725	GM12878	blood:	n/a	n/a
14	CHD1	chr1:179198345-179198918	IMR90	lung:	n/a	chr1:179198754-179198764
15	CHD2	chr1:179198092-179198228	K562	blood:	n/a	chr1:179198200-179198210
16	CHD2	chr1:179198953-179199173	H1-hESC	embryonic stem cell:	n/a	n/a
17	CHD2	chr1:179197835-179199176	Hela-S3	cervix:	n/a	chr1:179198754-179198764 chr1:179198311-179198321 chr1:179198200-179198210
18	CHD2	chr1:179198028-179198235	GM12878	blood:	n/a	chr1:179198200-179198210
19	CHD2	chr1:179198461-179198574	H1-hESC	embryonic stem cell:	n/a	n/a
20	CTCF	chr1:179197987-179198069	GM10248	blood:	n/a	n/a
21	CTCF	chr1:179198480-179198630	SK-N-SH_RA	brain:	n/a	chr1:179198563-179198573
22	CTCF	chr1:179199120-179199270	Hela-S3	cervix:	n/a	n/a
23	CTCF	chr1:179198220-179198370	AG04449	skin:	n/a	chr1:179198234-179198244
24	E2F4	chr1:179199166-179199780	MCF10A-Er-Src	breast:	n/a	n/a
25	E2F6	chr1:179198930-179199402	H1-hESC	embryonic stem cell:	n/a	n/a
26	E2F6	chr1:179198936-179199456	H1-hESC	embryonic stem cell:	n/a	n/a
27	E2F6	chr1:179198320-179199289	K562	blood:	n/a	chr1:179198756-179198765 chr1:179198693-179198703 chr1:179198551-179198560
28	E2F6	chr1:179198092-179199280	K562	blood:	n/a	chr1:179198756-179198765 chr1:179198693-179198703 chr1:179198551-179198560
29	EBF1	chr1:179197652-179197964	GM12878	blood:	n/a	n/a
30	EBF1	chr1:179197559-179197856	GM12878	blood:	n/a	n/a
31	EBF1	chr1:179199049-179199271	GM12878	blood:	n/a	n/a
32	EBF1	chr1:179199089-179199243	GM12878	blood:	n/a	n/a
33	EGR1	chr1:179198424-179198695	K562	blood:	n/a	chr1:179198552-179198565
34	EGR1	chr1:179197972-179198539	K562	blood:	n/a	chr1:179198159-179198173 chr1:179198251-179198261 chr1:179198251-179198264 chr1:179198251-179198264 chr1:179198330-179198340
35	EGR1	chr1:179197806-179198481	HCT-116	colon:	n/a	chr1:179198159-179198173 chr1:179198251-179198261 chr1:179198251-179198264 chr1:179198251-179198264 chr1:179198330-179198340
36	EGR1	chr1:179198705-179199029	GM12878	blood:	n/a	chr1:179198879-179198893
37	EGR1	chr1:179198044-179198298	GM12878	blood:	n/a	chr1:179198159-179198173 chr1:179198251-179198261 chr1:179198251-179198264 chr1:179198251-179198264
38	EGR1	chr1:179197974-179198332	H1-hESC	embryonic stem cell:	n/a	chr1:179198159-179198173 chr1:179198251-179198261 chr1:179198251-179198264 chr1:179198251-179198264
39	EGR1	chr1:179198856-179199155	K562	blood:	n/a	chr1:179199054-179199069 chr1:179198879-179198893 chr1:179199055-179199068
40	EGR1	chr1:179197898-179198398	K562	blood:	n/a	chr1:179198159-179198173 chr1:179198251-179198261 chr1:179198251-179198264 chr1:179198251-179198264 chr1:179198330-179198340
41	EGR1	chr1:179198837-179199193	K562	blood:	n/a	chr1:179199054-179199069 chr1:179198879-179198893 chr1:179199055-179199068
42	ELF1	chr1:179198663-179199117	K562	blood:	n/a	n/a
43	ELF1	chr1:179198349-179199296	GM12878	blood:	n/a	chr1:179198589-179198601
44	EP300	chr1:179199495-179200290	K562	blood:	n/a	chr1:179199505-179199514
45	EP300	chr1:179198384-179199010	ECC-1	luminal epithelium:	n/a	chr1:179198684-179198700
46	EP300	chr1:179200010-179200065	GM12878	blood:	n/a	n/a
47	ETS1	chr1:179198127-179198830	K562	blood:	n/a	chr1:179198161-179198172
48	FOS	chr1:179199445-179199894	MCF10A-Er-Src	breast:	n/a	chr1:179199681-179199692
49	FOS	chr1:179199424-179199882	HUVEC	blood vessel:	n/a	chr1:179199681-179199692
50	FOS	chr1:179199471-179199856	MCF10A-Er-Src	breast:	n/a	chr1:179199681-179199692

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:179198414-179198464	Caco-2	colon:	n/a
2	chr1:179198400-179198450	GM12892	blood:	n/a
3	chr1:179198964-179199014	AoSMC	blood vessel:	n/a
4	chr1:179199939-179199989	AG09319	gingival:	n/a
5	chr1:179198950-179199000	HRPEpiC	eye:	n/a
6	chr1:179198414-179198464	H1-hESC	embryonic stem cell:	embryo
7	chr1:179198964-179199014	SAEC	small airway:	n/a
8	chr1:179198964-179199014	HAEpiC	amniotic membrane:	n/a
9	chr1:179199424-179199474	GM19239	blood:	n/a
10	chr1:179198414-179198464	AG09309	skin:	n/a
11	chr1:179198400-179198450	NB4	blood:	n/a
12	chr1:179198105-179198155	ECC-1	luminal epithelium:	n/a
13	chr1:179198105-179198155	Caco-2	colon:	n/a
14	chr1:179198950-179199000	Caco-2	colon:	n/a
15	chr1:179198400-179198450	K562	blood:	n/a
16	chr1:179198950-179199000	SKMC	muscle:	n/a
17	chr1:179199424-179199474	K562	blood:	n/a
18	chr1:179199092-179199142	HNPCEpiC	eye:	n/a
19	chr1:179199199-179199249	HRPEpiC	eye:	n/a
20	chr1:179199424-179199474	H1-hESC	embryonic stem cell:	embryo
21	chr1:179199939-179199989	AG04450	lung:	fetal
22	chr1:179198964-179199014	NH-A	brain:	n/a
23	chr1:179199424-179199474	BJ	skin:	n/a
24	chr1:179199613-179199663	NT2-D1	testis:	n/a
25	chr1:179198964-179199014	NB4	blood:	n/a
26	chr1:179198964-179199014	HepG2	liver:	n/a
27	chr1:179199613-179199663	HIPEpiC	eye:	n/a
28	chr1:179198356-179198406	HMEC	breast:	n/a
29	chr1:179199939-179199989	MCF-7	breast:	n/a
30	chr1:179198400-179198450	HPAEpiC	pulmonary alveolar:	n/a
31	chr1:179198950-179199000	PrEC	prostate:	n/a
32	chr1:179199092-179199142	LNCaP	prostate:	n/a
33	chr1:179198414-179198464	AG09319	gingival:	n/a
34	chr1:179198356-179198406	Hela-S3	cervix:	n/a
35	chr1:179198356-179198406	AG09309	skin:	n/a
36	chr1:179198356-179198406	GM19239	blood:	n/a
37	chr1:179199092-179199142	SK-N-SH	brain:	n/a
38	chr1:179198105-179198155	AG09319	gingival:	n/a
39	chr1:179198105-179198155	AoSMC	blood vessel:	n/a
40	chr1:179198105-179198155	HUVEC	blood vessel:	n/a
41	chr1:179198356-179198406	BE2_C	brain:	n/a
42	chr1:179199092-179199142	U87	brain:	n/a
43	chr1:179199939-179199989	HCF	heart:	n/a
44	chr1:179199613-179199663	HAEpiC	amniotic membrane:	n/a
45	chr1:179199424-179199474	Jurkat	blood:	n/a
46	chr1:179198964-179199014	K562	blood:	n/a
47	chr1:179199199-179199249	MCF-7	breast:	n/a
48	chr1:179199613-179199663	PrEC	prostate:	n/a
49	chr1:179198400-179198450	HAEpiC	amniotic membrane:	n/a
50	chr1:179198950-179199000	BE2_C	brain:	n/a

No.	Distal block	Cell Line	Cell type
1	chr1:179194698..179198189-chr1:179199454..179203395,4	K562	blood:
2	chr1:179194698..179198189-chr1:179199454..179203395,4	K562	blood:
3	chr1:179198544..179200421-chr1:179334252..179336417,2	MCF-7	breast:
4	chr1:179168461..179170793-chr1:179198127..179200126,2	MCF-7	breast:
5	chr1:179187242..179191261-chr1:179196503..179201085,5	MCF-7	breast:
6	chr1:179059594..179062253-chr1:179196494..179198412,2	MCF-7	breast:
7	chr1:179181952..179183733-chr1:179196308..179198150,2	K562	blood:
8	chr1:179188599..179190144-chr1:179197953..179200570,2	MCF-7	breast:
9	chr1:179188852..179191101-chr1:179195980..179198204,2	K562	blood:
10	chr1:179189295..179193775-chr1:179196197..179201101,5	K562	blood:

Variant related genes	Relation type
ABL2	TF binding region
ABL2	CpG island
ENSG00000162779	chromatin interactions
ENSG00000201619	chromatin interactions
ENSG00000225711	chromatin interactions

Extended variants
information (count: 84 )
Associated
traits (count: 91 )

Variant overlapped rSNPs/rCNVs (count:84 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs111702334	chr1:179197623-179197624	Flanking Active TSS Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs561826760	chr1:179197631-179197632	Flanking Active TSS Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs147837691	chr1:179197645-179197646	Flanking Active TSS Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs560458160	chr1:179197712-179197713	Flanking Active TSS Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs548177621	chr1:179197730-179197731	Flanking Active TSS Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs141551972	chr1:179197827-179197828	Flanking Active TSS Active TSS Enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs548658179	chr1:179197837-179197838	Flanking Active TSS Active TSS Enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs562542125	chr1:179197913-179197914	Flanking Active TSS Active TSS Enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs531303464	chr1:179197929-179197930	Flanking Active TSS Active TSS Enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs573500456	chr1:179197955-179197956	Flanking Active TSS Active TSS Enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs369067747	chr1:179198003-179198004	Active TSS Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs551090224	chr1:179198023-179198024	Active TSS Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs570695306	chr1:179198030-179198031	Active TSS Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs567917362	chr1:179198112-179198113	Active TSS Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs539611279	chr1:179198193-179198194	Active TSS Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs546813066	chr1:179198201-179198202	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs566776736	chr1:179198202-179198203	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs28991587	chr1:179198204-179198205	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs28991586	chr1:179198300-179198301	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs367630647	chr1:179198358-179198359	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs544043509	chr1:179198393-179198394	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs371765591	chr1:179198416-179198417	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs61821692	chr1:179198439-179198440	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs558319702	chr1:179198445-179198446	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs368448205	chr1:179198449-179198450	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs578157802	chr1:179198467-179198468	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs540380154	chr1:179198609-179198610	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
28	rs2306941	chr1:179198653-179198654	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs573842159	chr1:179198675-179198676	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
30	rs555665593	chr1:179198767-179198768	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
31	rs66666828	chr1:179198768-179198769	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
32	rs3046363	chr1:179198789-179198790	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
33	rs10157417	chr1:179198864-179198865	Active TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
34	rs3122377	chr1:179198876-179198877	Active TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
35	rs28991584	chr1:179198962-179198963	Active TSS Flanking Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs28991583	chr1:179199007-179199008	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs28991582	chr1:179199008-179199009	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs575328251	chr1:179199036-179199037	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
39	rs200869162	chr1:179199056-179199057	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
40	rs373295470	chr1:179199062-179199063	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
41	rs564610686	chr1:179199063-179199064	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
42	rs527389353	chr1:179199067-179199068	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
43	rs2636265	chr1:179199076-179199077	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
44	rs561352980	chr1:179199111-179199112	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
45	rs574705867	chr1:179199116-179199117	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
46	rs370951425	chr1:179199129-179199130	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
47	rs12145184	chr1:179199191-179199192	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs377690264	chr1:179199234-179199235	Active TSS Flanking Active TSS Enhancers	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
49	rs529560498	chr1:179199284-179199285	Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
50	rs549681318	chr1:179199302-179199303	Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:91)

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
Cancer	21183584	CNVD
Multiple myeloma	16461302	CNVD
Rett syndrome	21593744	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
Glioblastoma multiforme	21080181	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
Acute myeloid leukemia	21251322	CNVD
Multiple myeloma	17550852	CNVD
Prostate cancer	18632612	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
Neuroblastoma	18923191	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Ewing''s sarcoma	17952124	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21509527	CNVD
Glioblastoma multiforme	17369134	CNVD
Cancer	17440070	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	21611746	CNVD
Breast cancer	16397240	CNVD
Mental retardation	17847001	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	23248035	CNVD
Metanephric adenoma	20802469	CNVD
Bipolar disorder	19114987	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:540 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:179157400-179197600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
2	chr1:179176200-179197600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr1:179176400-179197600	Weak transcription	Left Ventricle	heart
4	chr1:179177000-179197600	Weak transcription	HSMMtube	muscle
5	chr1:179178000-179197600	Weak transcription	Gastric	stomach
6	chr1:179178400-179197600	Weak transcription	HUES64 Cell Line	embryonic stem cell
7	chr1:179178600-179197600	Weak transcription	HUES6 Cell Line	embryonic stem cell
8	chr1:179178600-179197600	Weak transcription	NH-A	brain
9	chr1:179180200-179197600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
10	chr1:179181600-179197600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
11	chr1:179184400-179197600	Weak transcription	Fetal Thymus	thymus
12	chr1:179184800-179197600	Weak transcription	HMEC	breast
13	chr1:179185600-179197600	Weak transcription	HUES48 Cell Line	embryonic stem cell
14	chr1:179185800-179197600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
15	chr1:179186600-179197600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
16	chr1:179187600-179197600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
17	chr1:179187600-179197600	Weak transcription	HSMM	muscle
18	chr1:179187800-179197600	Weak transcription	Muscle Satellite Cultured Cells	--
19	chr1:179187800-179197600	Weak transcription	HUVEC	blood vessel
20	chr1:179188000-179197600	Weak transcription	Brain Anterior Caudate	brain
21	chr1:179188000-179197600	Weak transcription	Right Ventricle	heart
22	chr1:179188000-179197600	Weak transcription	Skeletal Muscle Female	skeletal muscle
23	chr1:179188000-179197600	Weak transcription	NHDF-Ad	bronchial
24	chr1:179188200-179197600	Weak transcription	Primary B cells from peripheral blood	blood
25	chr1:179188200-179197600	Weak transcription	NHLF	lung
26	chr1:179188400-179197600	Weak transcription	Primary monocytes fromperipheralblood	blood
27	chr1:179188400-179197600	Weak transcription	Lung	lung
28	chr1:179188400-179197600	Weak transcription	Psoas Muscle	Psoas
29	chr1:179188600-179197600	Weak transcription	H1 Cell Line	embryonic stem cell
30	chr1:179188600-179197600	Weak transcription	Primary hematopoietic stem cells	blood
31	chr1:179190600-179197600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
32	chr1:179191400-179197600	Weak transcription	Primary B cells from cord blood	blood
33	chr1:179191400-179197600	Weak transcription	Primary T cells from cord blood	blood
34	chr1:179194000-179197600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
35	chr1:179194200-179197600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
36	chr1:179194400-179197600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
37	chr1:179194400-179197600	Weak transcription	Fetal Stomach	stomach
38	chr1:179194600-179197600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
39	chr1:179195000-179197600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
40	chr1:179195000-179197800	Weak transcription	Placenta	Placenta
41	chr1:179195800-179197600	Enhancers	Liver	Liver
42	chr1:179196000-179197600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
43	chr1:179196000-179197600	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
44	chr1:179196000-179197600	Enhancers	Primary T helper naive cells fromperipheralblood	blood
45	chr1:179196000-179197600	Enhancers	Primary T helper cells PMA-I stimulated	--
46	chr1:179196000-179197600	Enhancers	Primary T killer naive cells fromperipheralblood	blood
47	chr1:179196200-179197600	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
48	chr1:179196200-179197600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
49	chr1:179196400-179197600	Enhancers	Primary T regulatory cells fromperipheralblood	blood
50	chr1:179196400-179197600	Enhancers	Brain Cingulate Gyrus	brain

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