Variant report

Variant	esv1841124
Chromosome Location	chr5:77937453-77944988
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:579)
CpG islands
(count:366)
Chromatin interactive
region (count:11)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:579 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr5:77936515-77937515	HepG2	liver:	n/a	n/a
2	ARID3A	chr5:77943837-77943868	HepG2	liver:	n/a	n/a
3	BACH1	chr5:77943329-77944203	H1-hESC	embryonic stem cell:	n/a	n/a
4	BCL11A	chr5:77943622-77943980	GM12878	blood:	n/a	chr5:77943877-77943886
5	BCLAF1	chr5:77943183-77944315	GM12878	blood:	n/a	chr5:77944064-77944077 chr5:77943877-77943886 chr5:77944281-77944294 chr5:77944068-77944081 chr5:77944068-77944081
6	BCLAF1	chr5:77943246-77944248	GM12878	blood:	n/a	chr5:77944064-77944077 chr5:77943877-77943886 chr5:77944068-77944081 chr5:77944068-77944081
7	BHLHE40	chr5:77944778-77944985	GM12878	blood:	n/a	chr5:77944890-77944906 chr5:77944895-77944911
8	BHLHE40	chr5:77943801-77943895	K562	blood:	n/a	n/a
9	BHLHE40	chr5:77943290-77943993	GM12878	blood:	n/a	n/a
10	BHLHE40	chr5:77944357-77944668	HepG2	liver:	n/a	n/a
11	BRCA1	chr5:77943089-77943306	Hela-S3	cervix:	n/a	n/a
12	BRCA1	chr5:77943784-77944110	Hela-S3	cervix:	n/a	n/a
13	CCNT2	chr5:77943698-77945144	K562	blood:	n/a	n/a
14	CEBPB	chr5:77941179-77941490	IMR90	lung:	n/a	chr5:77941327-77941340 chr5:77941327-77941338
15	CEBPB	chr5:77944302-77944476	Hela-S3	cervix:	n/a	n/a
16	CEBPB	chr5:77941151-77941463	HepG2	liver:	n/a	chr5:77941327-77941340 chr5:77941327-77941338
17	CEBPB	chr5:77943833-77944035	Hela-S3	cervix:	n/a	n/a
18	CEBPB	chr5:77943605-77943692	H1-hESC	embryonic stem cell:	n/a	n/a
19	CEBPB	chr5:77941177-77941480	A549	lung:	n/a	chr5:77941327-77941340 chr5:77941327-77941338
20	CEBPB	chr5:77941255-77941472	K562	blood:	n/a	chr5:77941327-77941340 chr5:77941327-77941338
21	CEBPD	chr5:77944264-77944761	HepG2	liver:	n/a	n/a
22	CHD1	chr5:77942547-77945482	IMR90	lung:	n/a	n/a
23	CHD1	chr5:77944979-77945152	GM12878	blood:	n/a	n/a
24	CHD1	chr5:77944075-77944256	H1-hESC	embryonic stem cell:	n/a	n/a
25	CHD1	chr5:77943257-77944553	GM12878	blood:	n/a	n/a
26	CHD1	chr5:77943445-77943775	H1-hESC	embryonic stem cell:	n/a	n/a
27	CHD2	chr5:77944483-77944673	HepG2	liver:	n/a	n/a
28	CHD2	chr5:77942841-77942912	GM12878	blood:	n/a	n/a
29	CHD2	chr5:77938531-77938574	K562	blood:	n/a	n/a
30	CHD2	chr5:77944340-77945022	GM12878	blood:	n/a	n/a
31	CHD2	chr5:77943939-77944073	GM12878	blood:	n/a	n/a
32	CHD2	chr5:77944946-77944949	HepG2	liver:	n/a	n/a
33	CHD2	chr5:77943828-77944774	Hela-S3	cervix:	n/a	n/a
34	CHD2	chr5:77944170-77944205	HepG2	liver:	n/a	n/a
35	CHD2	chr5:77938743-77938943	HepG2	liver:	n/a	n/a
36	CREB1	chr5:77943166-77943528	A549	lung:	n/a	n/a
37	CREB1	chr5:77944031-77945157	A549	lung:	n/a	n/a
38	CTBP2	chr5:77943776-77945110	H1-hESC	embryonic stem cell:	n/a	n/a
39	CTCF	chr5:77943960-77944110	GM12864	blood:	n/a	n/a
40	CTCF	chr5:77944520-77944670	GM12873	blood:	n/a	n/a
41	CTCF	chr5:77943914-77944132	GM19238	blood:	n/a	n/a
42	CTCF	chr5:77943980-77944130	AG09309	skin:	n/a	n/a
43	CTCF	chr5:77943940-77944090	SK-N-SH_RA	brain:	n/a	n/a
44	CTCF	chr5:77944300-77944450	AG04449	skin:	n/a	n/a
45	CTCF	chr5:77943700-77943850	RPTEC	kidney:	n/a	n/a
46	CTCF	chr5:77943940-77944090	GM12864	blood:	n/a	n/a
47	CTCF	chr5:77943980-77944130	HMF	breast:	n/a	n/a
48	CTCF	chr5:77943940-77944090	HCFaa	heart:	n/a	n/a
49	CTCF	chr5:77943660-77943810	RPTEC	kidney:	n/a	n/a
50	CTCF	chr5:77943970-77944075	Hela-S3	cervix:	n/a	n/a

(count:366 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:77943417-77943467	Hepatocyte	liver:	n/a
2	chr5:77943869-77943919	RPTEC	kidney:	n/a
3	chr5:77944343-77944393	GM12892	blood:	n/a
4	chr5:77940704-77940754	AG09309	skin:	n/a
5	chr5:77943869-77943919	NH-A	brain:	n/a
6	chr5:77943417-77943467	H1-hESC	embryonic stem cell:	embryo
7	chr5:77940704-77940754	GM12878	blood:	n/a
8	chr5:77940704-77940754	A549	lung:	n/a
9	chr5:77944343-77944393	HEK293	kidney:	embryo
10	chr5:77943786-77943836	H1-hESC	embryonic stem cell:	embryo
11	chr5:77944343-77944393	SKMC	muscle:	n/a
12	chr5:77944851-77944901	AG10803	skin:	n/a
13	chr5:77943869-77943919	T-47D	breast:	n/a
14	chr5:77940704-77940754	SK-N-MC	brain:	n/a
15	chr5:77943786-77943836	SKMC	muscle:	n/a
16	chr5:77940704-77940754	Caco-2	colon:	n/a
17	chr5:77940704-77940754	PFSK-1	brain:	n/a
18	chr5:77943417-77943467	ECC-1	luminal epithelium:	n/a
19	chr5:77944851-77944901	Hela-S3	cervix:	n/a
20	chr5:77940704-77940754	SK-N-SH	brain:	n/a
21	chr5:77944851-77944901	HL-60	blood:	n/a
22	chr5:77943417-77943467	GM19239	blood:	n/a
23	chr5:77943417-77943467	SK-N-SH_RA	brain:	n/a
24	chr5:77940704-77940754	HAEpiC	amniotic membrane:	n/a
25	chr5:77943417-77943467	IMR90	lung:	fetal
26	chr5:77944851-77944901	HNPCEpiC	eye:	n/a
27	chr5:77944851-77944901	HCF	heart:	n/a
28	chr5:77943417-77943467	SK-N-MC	brain:	n/a
29	chr5:77943417-77943467	HAEpiC	amniotic membrane:	n/a
30	chr5:77943417-77943467	AoSMC	blood vessel:	n/a
31	chr5:77943417-77943467	SAEC	small airway:	n/a
32	chr5:77944343-77944393	HRE	kidney:	n/a
33	chr5:77944851-77944901	AG04449	skin:	fetal
34	chr5:77944343-77944393	HCPEpiC	choroid plexus:	n/a
35	chr5:77940704-77940754	HRPEpiC	eye:	n/a
36	chr5:77943786-77943836	HEK293	kidney:	embryo
37	chr5:77943869-77943919	PFSK-1	brain:	n/a
38	chr5:77943417-77943467	HMEC	breast:	n/a
39	chr5:77943417-77943467	AG09309	skin:	n/a
40	chr5:77943786-77943836	Hela-S3	cervix:	n/a
41	chr5:77940704-77940754	SAEC	small airway:	n/a
42	chr5:77943869-77943919	NB4	blood:	n/a
43	chr5:77944343-77944393	SAEC	small airway:	n/a
44	chr5:77943869-77943919	HPAEpiC	pulmonary alveolar:	n/a
45	chr5:77944851-77944901	K562	blood:	n/a
46	chr5:77943786-77943836	HMEC	breast:	n/a
47	chr5:77940704-77940754	LNCaP	prostate:	n/a
48	chr5:77944343-77944393	PrEC	prostate:	n/a
49	chr5:77940704-77940754	SK-N-SH_RA	brain:	n/a
50	chr5:77943869-77943919	SKMC	muscle:	n/a

(count:11 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr5:77940516..77942352-chr5:77943015..77944536,2	MCF-7	breast:
2	chr5:77784933..77786634-chr5:77938068..77939590,2	K562	blood:
3	chr5:77936618..77938171-chr5:77943031..77945738,2	K562	blood:
4	chr5:77932938..77939935-chr5:77942023..77946135,10	MCF-7	breast:
5	chr5:77943376..77944358-chr9:107509480..107510026,2	Hela-S3	cervix:
6	chr5:77935729..77937549-chr5:77939132..77942017,2	K562	blood:
7	chr5:77940516..77942352-chr5:77943015..77944536,2	MCF-7	breast:
8	chr5:77938307..77940817-chr5:77941408..77943351,3	K562	blood:
9	chr5:77932938..77939935-chr5:77942023..77946135,10	MCF-7	breast:
10	chr5:77936618..77938171-chr5:77943031..77945738,2	K562	blood:
11	chr5:77944860..77948164-chr5:77958771..77961486,4	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ARSB-3	chr5:77937833-77937985	NONHSAT102334

No data

Variant related genes	Relation type
HMGB1P21	TF binding region
LHFPL2	TF binding region
HMGB1P21	CpG island
LHFPL2	CpG island
ENSG00000145685	chromatin interactions
ENSG00000248909	chromatin interactions
ENSG00000136783	chromatin interactions

Extended variants
information (count: 263 )
Associated
traits (count: 80 )

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	rs341930	chr5:77937453-77937454	Weak transcription Enhancers Transcr. at gene 5' and 3' Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs73769041	chr5:77937460-77937461	Weak transcription Enhancers Transcr. at gene 5' and 3' Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs531456896	chr5:77937558-77937559	Weak transcription Enhancers Transcr. at gene 5' and 3' Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs115132175	chr5:77937620-77937621	Weak transcription Active TSS Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs530224597	chr5:77937689-77937690	Weak transcription Active TSS Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs114167194	chr5:77937713-77937714	Weak transcription Active TSS Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs398109068	chr5:77937730-77937731	Weak transcription Active TSS Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs141791269	chr5:77937747-77937748	Weak transcription Active TSS Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs559207925	chr5:77937755-77937756	Weak transcription Active TSS Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs57178643	chr5:77937760-77937761	Weak transcription Active TSS Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs71001118	chr5:77937761-77937762	Weak transcription Active TSS Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs57050495	chr5:77937764-77937765	Weak transcription Active TSS Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs548078911	chr5:77937838-77937839	Weak transcription Enhancers Active TSS Strong transcription Genic enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
14	rs114608552	chr5:77937863-77937864	Weak transcription Enhancers Active TSS Strong transcription Genic enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
15	rs140180094	chr5:77937890-77937891	Weak transcription Enhancers Active TSS Strong transcription Genic enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
16	rs562058491	chr5:77937898-77937899	Weak transcription Enhancers Active TSS Strong transcription Genic enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
17	rs559077931	chr5:77937924-77937925	Weak transcription Enhancers Active TSS Strong transcription Genic enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
18	rs569221920	chr5:77937932-77937933	Weak transcription Enhancers Active TSS Strong transcription Genic enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
19	rs191771995	chr5:77937994-77937995	Weak transcription Enhancers Active TSS Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs554143373	chr5:77938004-77938005	Weak transcription Active TSS Strong transcription Genic enhancers Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs370278483	chr5:77938006-77938007	Weak transcription Active TSS Strong transcription Genic enhancers Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs371259648	chr5:77938079-77938080	Weak transcription Active TSS Strong transcription Genic enhancers Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs78051860	chr5:77938095-77938096	Weak transcription Active TSS Strong transcription Genic enhancers Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs576848104	chr5:77938096-77938097	Weak transcription Active TSS Strong transcription Genic enhancers Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs184693588	chr5:77938098-77938099	Weak transcription Active TSS Strong transcription Genic enhancers Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs573168406	chr5:77938142-77938143	Weak transcription Active TSS Strong transcription Genic enhancers Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs531648332	chr5:77938143-77938144	Weak transcription Active TSS Strong transcription Genic enhancers Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs527278633	chr5:77938149-77938150	Weak transcription Active TSS Strong transcription Genic enhancers Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs74510210	chr5:77938160-77938161	Weak transcription Active TSS Strong transcription Genic enhancers Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs561963804	chr5:77938163-77938164	Weak transcription Active TSS Strong transcription Genic enhancers Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs76393772	chr5:77938185-77938186	Weak transcription Active TSS Strong transcription Genic enhancers Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs530159627	chr5:77938188-77938189	Weak transcription Active TSS Strong transcription Genic enhancers Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs546959140	chr5:77938199-77938200	Weak transcription Active TSS Strong transcription Genic enhancers Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs116464201	chr5:77938204-77938205	Weak transcription Enhancers Active TSS Strong transcription Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs532602530	chr5:77938257-77938258	Weak transcription Enhancers Active TSS Strong transcription Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs187470002	chr5:77938261-77938262	Weak transcription Enhancers Active TSS Strong transcription Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs569059484	chr5:77938272-77938273	Weak transcription Enhancers Active TSS Strong transcription Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs538043593	chr5:77938278-77938279	Weak transcription Enhancers Active TSS Strong transcription Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs143861211	chr5:77938285-77938286	Weak transcription Enhancers Active TSS Strong transcription Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs115947689	chr5:77938296-77938297	Weak transcription Enhancers Active TSS Strong transcription Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs146394450	chr5:77938297-77938298	Weak transcription Enhancers Active TSS Strong transcription Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs192609171	chr5:77938327-77938328	Weak transcription Enhancers Active TSS Strong transcription Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs139484609	chr5:77938329-77938330	Weak transcription Enhancers Active TSS Strong transcription Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs553698834	chr5:77938396-77938397	Weak transcription Enhancers Active TSS Strong transcription Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs185647519	chr5:77938405-77938406	Weak transcription Enhancers Genic enhancers Active TSS Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs190507001	chr5:77938420-77938421	Weak transcription Enhancers Genic enhancers Active TSS Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs556397572	chr5:77938421-77938422	Weak transcription Enhancers Genic enhancers Active TSS Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs202083786	chr5:77938448-77938449	Weak transcription Enhancers Genic enhancers Active TSS Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs142811359	chr5:77938524-77938525	Weak transcription Enhancers Genic enhancers Active TSS Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs151058558	chr5:77938570-77938571	Weak transcription Enhancers Genic enhancers Active TSS Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:80)

Disease	PMID	Source
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Metanephric adenoma	20802469	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Medulloblastoma	21979893	CNVD
Phyllodes tumor	17334353	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Cancer	16751803	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	17603634	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Melanoma	18172304	CNVD
Glioma	20126413	CNVD
Breast cancer	22032731	CNVD
Congenital anomalies of the kidney and urinary tract	18694510	CNVD
Prostate cancer	21965145	CNVD
Ovarian cancer	20844748	CNVD
Breast cancer	17393978	CNVD
Cancer	21359685	CNVD
Non-small cell lung cancer	21829676	CNVD
adenomatous polyposis	22470819	CNVD
Cancer	22429812	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Liposarcoma	21253554	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Breast cancer	21858162	CNVD
Leukemia	17361228	CNVD
Myelodysplastic syndrome	18508791	CNVD
5q-syndrome	17576883	CNVD
Gastric cancer	17908304	CNVD
Lung cancer	16740712	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Urothelial carcinoma	21177765	CNVD
Oral cancer	21386901	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Barrett''s syndrome	19417022	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Breast cancer	19602461	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Retinoblastoma	22278416	CNVD
Bipolar disorder	18458673	CNVD
Thyroid cancer	19087340	CNVD
Breast cancer	21785460	CNVD
Merkel cell carcinoma	19020549	CNVD
Squamous cell cancer	20885788	CNVD
Hepatocellular carcinoma	16750200	CNVD
Neurodevelopmental disorder	22521361	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	17133270	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Acute myeloid leukemia	20729466	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Ovarian cancer	21720365	CNVD
Acute myeloid leukemia	21251322	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Myelofibrosis	22110671	CNVD
craniofacial dysmorphism	21918468	CNVD
lymphocytic leukemia	21291569	CNVD
Lung cancer	16773561	CNVD
Multiple myeloma	16616336	CNVD
Testicular cancer	18059402	CNVD
Colorectal cancer	16272173	CNVD
Prostate cancer	16573809	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:671 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:77928200-77942400	Weak transcription	Primary B cells from cord blood	blood
2	chr5:77930600-77938000	Enhancers	Breast Myoepithelial Primary Cells	Breast
3	chr5:77931000-77942800	Weak transcription	K562	blood
4	chr5:77932200-77937800	Enhancers	Fetal Intestine Small	intestine
5	chr5:77932400-77938600	Enhancers	Fetal Intestine Large	intestine
6	chr5:77932800-77938200	Enhancers	HMEC	breast
7	chr5:77933800-77938000	Enhancers	Fetal Muscle Leg	muscle
8	chr5:77933800-77940600	Weak transcription	Placenta	Placenta
9	chr5:77933800-77941400	Weak transcription	Right Atrium	heart
10	chr5:77933800-77943200	Weak transcription	Esophagus	oesophagus
11	chr5:77934600-77940600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
12	chr5:77934600-77942400	Weak transcription	Colonic Mucosa	Colon
13	chr5:77934800-77937600	Transcr. at gene 5' and 3'	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
14	chr5:77935000-77938400	Weak transcription	Fetal Muscle Trunk	muscle
15	chr5:77935200-77940400	Weak transcription	Brain Inferior Temporal Lobe	brain
16	chr5:77935200-77942000	Weak transcription	Right Ventricle	heart
17	chr5:77935200-77942600	Weak transcription	Placenta Amnion	Placenta Amnion
18	chr5:77935400-77942000	Weak transcription	Skeletal Muscle Male	skeletal muscle
19	chr5:77935400-77942600	Weak transcription	Rectal Mucosa Donor 29	rectum
20	chr5:77936000-77942600	Weak transcription	Fetal Brain Female	brain
21	chr5:77936400-77937600	Transcr. at gene 5' and 3'	A549	lung
22	chr5:77936600-77937600	Genic enhancers	iPS-18 Cell Line	embryonic stem cell
23	chr5:77936600-77937600	Genic enhancers	Fetal Lung	lung
24	chr5:77936600-77939000	Enhancers	Duodenum Mucosa	Duodenum
25	chr5:77936600-77939000	Enhancers	Pancreas	Pancrea
26	chr5:77936800-77937600	Flanking Active TSS	GM12878-XiMat	blood
27	chr5:77936800-77940400	Weak transcription	Brain Anterior Caudate	brain
28	chr5:77936800-77940600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
29	chr5:77936800-77940800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
30	chr5:77937000-77937600	Enhancers	ES-WA7 Cell Line	embryonic stem cell
31	chr5:77937000-77938200	Weak transcription	Thymus	Thymus
32	chr5:77937000-77939000	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
33	chr5:77937000-77940400	Weak transcription	Hela-S3	cervix
34	chr5:77937000-77940600	Weak transcription	Aorta	Aorta
35	chr5:77937000-77942600	Weak transcription	Left Ventricle	heart
36	chr5:77937000-77942600	Weak transcription	Skeletal Muscle Female	skeletal muscle
37	chr5:77937000-77943200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
38	chr5:77937000-77943200	Weak transcription	Psoas Muscle	Psoas
39	chr5:77937200-77937600	Enhancers	Fetal Kidney	kidney
40	chr5:77937200-77937800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
41	chr5:77937200-77937800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
42	chr5:77937200-77938000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
43	chr5:77937200-77938000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
44	chr5:77937200-77938000	Weak transcription	Primary B cells from peripheral blood	blood
45	chr5:77937200-77938200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
46	chr5:77937200-77938200	Weak transcription	Fetal Thymus	thymus
47	chr5:77937200-77938400	Weak transcription	H9 Cell Line	embryonic stem cell
48	chr5:77937200-77938400	Weak transcription	Fetal Stomach	stomach
49	chr5:77937200-77938600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
50	chr5:77937200-77938600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell

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