Variant report

Variant	nsv1031881
Chromosome Location	chr5:75917033-75946265
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:387)
CpG islands
(count:430)
Chromatin interactive
region (count:22)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:387 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr5:75918808-75918857	K562	blood:	n/a	n/a
2	ATF1	chr5:75921493-75921693	K562	blood:	n/a	n/a
3	BACH1	chr5:75919062-75919399	H1-hESC	embryonic stem cell:	n/a	chr5:75919255-75919269
4	BHLHE40	chr5:75921359-75921598	K562	blood:	n/a	n/a
5	BRCA1	chr5:75936794-75936839	GM12878	blood:	n/a	n/a
6	CBX3	chr5:75945721-75946038	K562	blood:	n/a	n/a
7	CCNT2	chr5:75921389-75921620	K562	blood:	n/a	n/a
8	CEBPB	chr5:75919012-75919469	IMR90	lung:	n/a	chr5:75919083-75919096
9	CEBPB	chr5:75919008-75919438	A549	lung:	n/a	chr5:75919083-75919096
10	CEBPB	chr5:75928718-75928908	A549	lung:	n/a	chr5:75928880-75928893
11	CEBPB	chr5:75918911-75919556	A549	lung:	n/a	chr5:75919083-75919096
12	CEBPB	chr5:75921361-75921566	K562	blood:	n/a	n/a
13	CEBPB	chr5:75919119-75919434	Hela-S3	cervix:	n/a	n/a
14	CEBPD	chr5:75921215-75921671	K562	blood:	n/a	n/a
15	CEBPD	chr5:75921323-75921764	K562	blood:	n/a	n/a
16	CTCF	chr5:75937420-75937570	HA-sp	spinal cord:	n/a	chr5:75937530-75937546
17	CTCF	chr5:75937421-75937656	HepG2	liver:	n/a	chr5:75937530-75937546
18	CTCF	chr5:75937480-75937630	AG09309	skin:	n/a	chr5:75937530-75937546
19	CTCF	chr5:75937460-75937610	AoAF	blood vessel:	n/a	chr5:75937530-75937546
20	CTCF	chr5:75937440-75937590	GM06990	blood:	n/a	chr5:75937530-75937546
21	CTCF	chr5:75937409-75937581	SK-N-SH_RA	brain:	n/a	chr5:75937530-75937546
22	CTCF	chr5:75937411-75937675	K562	blood:	n/a	chr5:75937530-75937546
23	CTCF	chr5:75936540-75936690	HFF	foreskin:	n/a	n/a
24	CTCF	chr5:75937480-75937630	NHDF-neo	bronchial:	n/a	chr5:75937530-75937546
25	CTCF	chr5:75937480-75937630	K562	blood:	n/a	chr5:75937530-75937546
26	CTCF	chr5:75937437-75937652	ProgFib	skin:	n/a	chr5:75937530-75937546
27	CTCF	chr5:75937061-75937990	SK-N-SH	brain:	n/a	chr5:75937530-75937546
28	CTCF	chr5:75937480-75937630	HEK293	kidney:	n/a	chr5:75937530-75937546
29	CTCF	chr5:75937264-75937797	K562	blood:	n/a	chr5:75937530-75937546
30	CTCF	chr5:75937500-75937650	GM12868	blood:	n/a	chr5:75937530-75937546
31	CTCF	chr5:75937480-75937630	GM12864	blood:	n/a	chr5:75937530-75937546
32	CTCF	chr5:75937440-75937590	AoAF	blood vessel:	n/a	chr5:75937530-75937546
33	CTCF	chr5:75938000-75938150	HPAF	blood vessel:	n/a	n/a
34	CTCF	chr5:75937447-75937693	T-47D	breast:	n/a	chr5:75937530-75937546
35	CTCF	chr5:75937420-75937570	GM12864	blood:	n/a	chr5:75937530-75937546
36	CTCF	chr5:75937288-75937722	T-47D	breast:	n/a	chr5:75937530-75937546
37	CTCF	chr5:75937420-75937570	HL-60	blood:	n/a	chr5:75937530-75937546
38	CTCF	chr5:75937455-75937610	GM19239	blood:	n/a	chr5:75937530-75937546
39	CTCF	chr5:75937414-75937660	GM13977	blood:	n/a	chr5:75937530-75937546
40	CTCF	chr5:75937460-75937610	GM06990	blood:	n/a	chr5:75937530-75937546
41	CTCF	chr5:75937395-75937628	HepG2	liver:	n/a	chr5:75937530-75937546
42	CTCF	chr5:75937481-75937575	GM19238	blood:	n/a	chr5:75937530-75937546
43	CTCF	chr5:75937760-75937910	HVMF	connective:	n/a	n/a
44	CTCF	chr5:75937460-75937610	HMEC	breast:	n/a	chr5:75937530-75937546
45	CTCF	chr5:75937420-75937570	HFF-Myc	foreskin:	n/a	chr5:75937530-75937546
46	CTCF	chr5:75937500-75937650	NHEK	skin:	n/a	chr5:75937530-75937546
47	CTCF	chr5:75937440-75937590	HFF-Myc	foreskin:	n/a	chr5:75937530-75937546
48	CTCF	chr5:75937303-75937912	IMR90	lung:	n/a	chr5:75937530-75937546
49	CTCF	chr5:75937440-75937590	GM12871	blood:	n/a	chr5:75937530-75937546
50	CTCF	chr5:75930645-75930716	HUVEC	blood vessel:	n/a	chr5:75930671-75930687 chr5:75930665-75930686

(count:430 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:75919481-75919531	IMR90	lung:	fetal
2	chr5:75918112-75918162	SKMC	muscle:	n/a
3	chr5:75919850-75919900	IMR90	lung:	fetal
4	chr5:75919481-75919531	IMR90	lung:	fetal
5	chr5:75918112-75918162	SKMC	muscle:	n/a
6	chr5:75919850-75919900	IMR90	lung:	fetal
7	chr5:75919242-75919292	HepG2	liver:	n/a
8	chr5:75919242-75919292	HMEC	breast:	n/a
9	chr5:75938513-75938563	PrEC	prostate:	n/a
10	chr5:75938513-75938563	NHDF-neo	bronchial:	n/a
11	chr5:75919850-75919900	AG09319	gingival:	n/a
12	chr5:75919850-75919900	Hela-S3	cervix:	n/a
13	chr5:75919850-75919900	NH-A	brain:	n/a
14	chr5:75919850-75919900	NHBE	bronchial:	n/a
15	chr5:75919188-75919238	U87	brain:	n/a
16	chr5:75919850-75919900	PFSK-1	brain:	n/a
17	chr5:75919281-75919331	BE2_C	brain:	n/a
18	chr5:75918112-75918162	LNCaP	prostate:	n/a
19	chr5:75919242-75919292	HEEpiC	esophagus:	n/a
20	chr5:75919242-75919292	HCM	heart:	n/a
21	chr5:75919188-75919238	PrEC	prostate:	n/a
22	chr5:75938513-75938563	BE2_C	brain:	n/a
23	chr5:75938513-75938563	HIPEpiC	eye:	n/a
24	chr5:75919850-75919900	Caco-2	colon:	n/a
25	chr5:75938513-75938563	NH-A	brain:	n/a
26	chr5:75919281-75919331	Jurkat	blood:	n/a
27	chr5:75938513-75938563	ECC-1	luminal epithelium:	n/a
28	chr5:75919188-75919238	LNCaP	prostate:	n/a
29	chr5:75919281-75919331	AG10803	skin:	n/a
30	chr5:75918112-75918162	HL-60	blood:	n/a
31	chr5:75919188-75919238	HCM	heart:	n/a
32	chr5:75938513-75938563	BJ	skin:	n/a
33	chr5:75938513-75938563	HCT-116	colon:	n/a
34	chr5:75919242-75919292	MCF10A-Er-Src	breast:	n/a
35	chr5:75919188-75919238	SKMC	muscle:	n/a
36	chr5:75919281-75919331	HCPEpiC	choroid plexus:	n/a
37	chr5:75919281-75919331	U87	brain:	n/a
38	chr5:75919281-75919331	PFSK-1	brain:	n/a
39	chr5:75918112-75918162	AG04449	skin:	fetal
40	chr5:75938513-75938563	HAEpiC	amniotic membrane:	n/a
41	chr5:75918112-75918162	NH-A	brain:	n/a
42	chr5:75919188-75919238	HCT-116	colon:	n/a
43	chr5:75919281-75919331	T-47D	breast:	n/a
44	chr5:75919281-75919331	NHDF-neo	bronchial:	n/a
45	chr5:75918112-75918162	Caco-2	colon:	n/a
46	chr5:75919850-75919900	Hepatocyte	liver:	n/a
47	chr5:75919242-75919292	LNCaP	prostate:	n/a
48	chr5:75919281-75919331	GM06990	blood:	n/a
49	chr5:75919481-75919531	BJ	skin:	n/a
50	chr5:75938513-75938563	HCF	heart:	n/a

(count:22 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr5:75921709..75924206-chr5:75928955..75931942,2	K562	blood:
2	chr5:75914946..75917081-chr5:75935923..75937441,2	K562	blood:
3	chr5:75927707..75929227-chr5:75935967..75938203,2	K562	blood:
4	chr5:75925160..75926957-chr5:75929982..75931882,2	MCF-7	breast:
5	chr5:75926553..75929296-chr5:75932910..75934652,2	K562	blood:
6	chr5:75926553..75929296-chr5:75932910..75934652,2	K562	blood:
7	chr5:75896478..75897915-chr5:75936605..75938172,9	MCF-7	breast:
8	chr5:75921709..75924206-chr5:75928955..75931942,2	K562	blood:
9	chr5:75914946..75917081-chr5:75935923..75937441,2	K562	blood:
10	chr5:75903037..75905690-chr5:75932365..75935110,2	K562	blood:
11	chr5:75934487..75936821-chr5:75943605..75946585,2	MCF-7	breast:
12	chr5:75927707..75929227-chr5:75935967..75938203,2	K562	blood:
13	chr5:75896964..75897974-chr5:75936696..75938042,13	K562	blood:
14	chr5:75897979..75898810-chr5:75937080..75938018,3	K562	blood:
15	chr5:75897714..75898323-chr5:75934762..75935296,2	MCF-7	breast:
16	chr5:75910340..75912765-chr5:75915221..75917269,3	K562	blood:
17	chr5:75937138..75939935-chr5:76031767..76034422,2	K562	blood:
18	chr5:75897975..75898494-chr5:75937296..75938025,2	MCF-7	breast:
19	chr5:75934487..75936821-chr5:75943605..75946585,2	MCF-7	breast:
20	chr5:75633387..75634022-chr5:75937052..75937701,2	K562	blood:
21	chr5:75925160..75926957-chr5:75929982..75931882,2	MCF-7	breast:
22	chr5:75897247..75898569-chr5:75937033..75938017,10	MCF-7	breast:

No data

Variant related genes	Relation type
F2RL2	TF binding region
IQGAP2	TF binding region
F2RL2	CpG island
IQGAP2	CpG island
ENSG00000145703	chromatin interactions
ENSG00000249713	chromatin interactions

Extended variants
information (count: 1204 )
Associated
traits (count: 86 )

Variant overlapped rSNPs/rCNVs (count:1204 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2069697	chr5:75917033-75917034	Weak transcription Active TSS Enhancers Strong transcription Genic enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs571289488	chr5:75917035-75917036	Weak transcription Active TSS Enhancers Strong transcription Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs114754575	chr5:75917036-75917037	Weak transcription Active TSS Enhancers Strong transcription Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs2069659	chr5:75917052-75917053	Weak transcription Active TSS Enhancers Strong transcription Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs140884155	chr5:75917058-75917059	Weak transcription Active TSS Enhancers Strong transcription Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs541198924	chr5:75917088-75917089	Weak transcription Active TSS Enhancers Strong transcription Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs150178893	chr5:75917089-75917090	Weak transcription Active TSS Enhancers Strong transcription Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs537392890	chr5:75917109-75917110	Weak transcription Active TSS Enhancers Strong transcription Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs533255293	chr5:75917126-75917127	Weak transcription Active TSS Enhancers Strong transcription Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs2069658	chr5:75917302-75917303	Enhancers Weak transcription Active TSS Strong transcription Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	mRNA abundance
11	rs138522234	chr5:75917339-75917340	Enhancers Weak transcription Active TSS Strong transcription Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs574183719	chr5:75917366-75917367	Enhancers Weak transcription Active TSS Strong transcription Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs2069657	chr5:75917368-75917369	Enhancers Weak transcription Active TSS Strong transcription Genic enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs7702757	chr5:75917384-75917385	Enhancers Weak transcription Active TSS Strong transcription Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs555139737	chr5:75917413-75917414	Enhancers Weak transcription Active TSS Strong transcription Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs141564806	chr5:75917421-75917422	Enhancers Weak transcription Active TSS Strong transcription Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs3797397	chr5:75917519-75917520	Enhancers Weak transcription Active TSS Strong transcription Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs565786418	chr5:75917520-75917521	Enhancers Weak transcription Active TSS Strong transcription Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs533617849	chr5:75917539-75917540	Enhancers Weak transcription Active TSS Strong transcription Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs137949468	chr5:75917543-75917544	Enhancers Weak transcription Active TSS Strong transcription Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs2069656	chr5:75917633-75917634	Enhancers Weak transcription Active TSS Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs190246632	chr5:75917644-75917645	Enhancers Weak transcription Active TSS Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs537302614	chr5:75917659-75917660	Enhancers Weak transcription Active TSS Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs557242643	chr5:75917660-75917661	Enhancers Weak transcription Active TSS Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs567289537	chr5:75917661-75917662	Enhancers Weak transcription Active TSS Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs149395279	chr5:75917665-75917666	Enhancers Weak transcription Active TSS Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs553121440	chr5:75917672-75917673	Enhancers Weak transcription Active TSS Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs573272915	chr5:75917674-75917675	Enhancers Weak transcription Active TSS Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs545211098	chr5:75917677-75917678	Enhancers Weak transcription Active TSS Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs144792318	chr5:75917699-75917700	Enhancers Weak transcription Active TSS Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs148154724	chr5:75917703-75917704	Enhancers Weak transcription Active TSS Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs2069655	chr5:75917720-75917721	Enhancers Weak transcription Active TSS Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	mRNA abundance
33	rs543699685	chr5:75917801-75917802	Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs543380555	chr5:75917829-75917830	Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs528853631	chr5:75917851-75917852	Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs370292915	chr5:75917968-75917969	Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs563484087	chr5:75917982-75917983	Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs2069654	chr5:75917993-75917994	Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs397833008	chr5:75917994-75917995	Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs181983610	chr5:75917995-75917996	Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs2069653	chr5:75918000-75918001	Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs80016717	chr5:75918027-75918028	Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs2069652	chr5:75918032-75918033	Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs551067860	chr5:75918042-75918043	Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs367859520	chr5:75918047-75918048	Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs2069651	chr5:75918048-75918049	Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs184983502	chr5:75918090-75918091	Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs114137579	chr5:75918096-75918097	Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs2069650	chr5:75918113-75918114	Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs567927991	chr5:75918117-75918118	Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:86)

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
Myeloproliferative neoplasm	20015882	CNVD
Breast cancer	17603634	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Melanoma	18172304	CNVD
Glioma	20126413	CNVD
Breast cancer	22032731	CNVD
Prostate cancer	21965145	CNVD
Spinal muscular atrophy	21762474	CNVD
Esophageal cancer	20955586	CNVD
Congenital anomalies of the kidney and urinary tract	18694510	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
Hepatocellular carcinoma	16750200	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
Neurodevelopmental disorder	22521361	CNVD
Prostate cancer	18632612	CNVD
Spinal muscular atrophy	15981080	CNVD
Spinal muscular atrophy	18839960	CNVD
Spinal muscular atrophy	19716110	CNVD
Glioblastoma multiforme	22286061	CNVD
craniofacial dysmorphism	21918468	CNVD
Multiple myeloma	16616336	CNVD
Prostate cancer	16461572	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
Myelofibrosis	22110671	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Schizophrenia	23813976	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:656 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:75879000-75917600	Weak transcription	Fetal Thymus	thymus
2	chr5:75879000-75934000	Weak transcription	Small Intestine	intestine
3	chr5:75879200-75919000	Weak transcription	H9 Cell Line	embryonic stem cell
4	chr5:75880200-75933400	Strong transcription	Monocytes-CD14+_RO01746	blood
5	chr5:75882600-75969400	Weak transcription	Stomach Mucosa	stomach
6	chr5:75884400-75919200	Strong transcription	Primary monocytes fromperipheralblood	blood
7	chr5:75884400-75919400	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
8	chr5:75902600-75919200	Strong transcription	Primary T cells from cord blood	blood
9	chr5:75903600-75917800	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
10	chr5:75903800-75917800	Weak transcription	Rectal Smooth Muscle	rectum
11	chr5:75903800-75918800	Weak transcription	Fetal Kidney	kidney
12	chr5:75903800-75918800	Weak transcription	Stomach Smooth Muscle	stomach
13	chr5:75903800-75936200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
14	chr5:75903800-75943600	Weak transcription	Spleen	Spleen
15	chr5:75905200-75919000	Weak transcription	Cortex derived primary cultured neurospheres	brain
16	chr5:75907600-75923000	Weak transcription	Placenta	Placenta
17	chr5:75907800-75934600	Weak transcription	Rectal Mucosa Donor 31	rectum
18	chr5:75908000-75918000	Weak transcription	Duodenum Smooth Muscle	Duodenum
19	chr5:75908000-75918800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
20	chr5:75908000-75919000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
21	chr5:75908000-75919000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
22	chr5:75908000-75928000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
23	chr5:75909000-75923200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
24	chr5:75909200-75923000	Weak transcription	Lung	lung
25	chr5:75910200-75917400	Weak transcription	Fetal Intestine Small	intestine
26	chr5:75910200-75919000	Weak transcription	HUES6 Cell Line	embryonic stem cell
27	chr5:75910200-75921200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
28	chr5:75911200-75923000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
29	chr5:75911800-75918200	Strong transcription	Primary hematopoietic stem cells short term culture	blood
30	chr5:75912000-75917800	Weak transcription	Rectal Mucosa Donor 29	rectum
31	chr5:75913400-75934600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
32	chr5:75913600-75917200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
33	chr5:75914000-75919000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
34	chr5:75914000-75921800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
35	chr5:75914200-75917200	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
36	chr5:75914200-75917400	Weak transcription	NH-A	brain
37	chr5:75914200-75918000	Weak transcription	Fetal Intestine Large	intestine
38	chr5:75914200-75919600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
39	chr5:75914200-75953800	Weak transcription	Colonic Mucosa	Colon
40	chr5:75914400-75917200	Weak transcription	Fetal Stomach	stomach
41	chr5:75914400-75917800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
42	chr5:75914400-75919000	Weak transcription	Pancreas	Pancrea
43	chr5:75914400-75922600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
44	chr5:75914400-75922600	Weak transcription	Gastric	stomach
45	chr5:75914400-75922800	Weak transcription	Sigmoid Colon	Sigmoid Colon
46	chr5:75914400-75932800	Weak transcription	HepG2	liver
47	chr5:75914800-75919000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
48	chr5:75915000-75919400	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
49	chr5:75915000-75923000	Weak transcription	Duodenum Mucosa	Duodenum
50	chr5:75915000-75923200	Weak transcription	Primary neutrophils fromperipheralblood	blood

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