Variant report

Variant	nsv968910
Chromosome Location	chr5:49961360-49980983
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:649)
CpG islands
(count:855)
Chromatin interactive
region (count:11)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:649 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr5:49963625-49963798	HepG2	liver:	n/a	n/a
2	ATF2	chr5:49963638-49964245	GM12878	blood:	n/a	n/a
3	ATF2	chr5:49963313-49964267	GM12878	blood:	n/a	n/a
4	BACH1	chr5:49962169-49962903	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr5:49963175-49963321	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr5:49963742-49963776	H1-hESC	embryonic stem cell:	n/a	n/a
7	BATF	chr5:49961424-49962086	GM12878	blood:	n/a	n/a
8	BATF	chr5:49980862-49981362	GM12878	blood:	n/a	n/a
9	BATF	chr5:49963795-49964158	GM12878	blood:	n/a	n/a
10	BATF	chr5:49980938-49981231	GM12878	blood:	n/a	n/a
11	BATF	chr5:49961434-49961901	GM12878	blood:	n/a	n/a
12	BATF	chr5:49963191-49964388	GM12878	blood:	n/a	n/a
13	BATF	chr5:49962882-49963112	GM12878	blood:	n/a	n/a
14	BCL11A	chr5:49963147-49964513	GM12878	blood:	n/a	chr5:49963441-49963454 chr5:49963662-49963671
15	BCL11A	chr5:49963190-49963807	GM12878	blood:	n/a	chr5:49963441-49963454 chr5:49963662-49963671
16	BCL11A	chr5:49962597-49963034	GM12878	blood:	n/a	n/a
17	BCL11A	chr5:49963838-49964265	GM12878	blood:	n/a	n/a
18	BCL11A	chr5:49961450-49961802	GM12878	blood:	n/a	chr5:49961720-49961729
19	BCL11A	chr5:49961472-49961950	GM12878	blood:	n/a	chr5:49961720-49961729
20	BCL11A	chr5:49980916-49981312	GM12878	blood:	n/a	n/a
21	BCL11A	chr5:49962570-49962983	GM12878	blood:	n/a	n/a
22	BCL11A	chr5:49980852-49981333	GM12878	blood:	n/a	n/a
23	BCL3	chr5:49963498-49963956	GM12878	blood:	n/a	chr5:49963662-49963671
24	BCLAF1	chr5:49962387-49962943	GM12878	blood:	n/a	chr5:49962434-49962447 chr5:49962538-49962551 chr5:49962542-49962555 chr5:49962441-49962454
25	BCLAF1	chr5:49963087-49964265	GM12878	blood:	n/a	chr5:49963441-49963454 chr5:49963662-49963671 chr5:49963090-49963103
26	BHLHE40	chr5:49961650-49961980	GM12878	blood:	n/a	n/a
27	BHLHE40	chr5:49962310-49962966	GM12878	blood:	n/a	chr5:49962437-49962453 chr5:49962350-49962366 chr5:49962434-49962450 chr5:49962398-49962414 chr5:49962351-49962367 chr5:49962358-49962374
28	BHLHE40	chr5:49963184-49964201	GM12878	blood:	n/a	chr5:49963349-49963365
29	BRCA1	chr5:49963479-49963679	GM12878	blood:	n/a	n/a
30	BRCA1	chr5:49963601-49963771	H1-hESC	embryonic stem cell:	n/a	n/a
31	CEBPB	chr5:49963183-49964132	HepG2	liver:	n/a	n/a
32	CEBPB	chr5:49962527-49962687	HepG2	liver:	n/a	n/a
33	CEBPB	chr5:49961899-49961967	HepG2	liver:	n/a	n/a
34	CEBPB	chr5:49963187-49963458	HepG2	liver:	n/a	n/a
35	CEBPB	chr5:49963628-49964419	GM12878	blood:	n/a	n/a
36	CEBPB	chr5:49963065-49963619	A549	lung:	n/a	n/a
37	CEBPB	chr5:49963790-49964272	Hela-S3	cervix:	n/a	n/a
38	CEBPB	chr5:49963170-49963575	HepG2	liver:	n/a	n/a
39	CEBPB	chr5:49962596-49962783	H1-hESC	embryonic stem cell:	n/a	n/a
40	CEBPB	chr5:49963291-49963498	HepG2	liver:	n/a	n/a
41	CEBPB	chr5:49963010-49964128	H1-hESC	embryonic stem cell:	n/a	n/a
42	CEBPB	chr5:49963167-49963458	A549	lung:	n/a	n/a
43	CEBPB	chr5:49963251-49963503	K562	blood:	n/a	n/a
44	CEBPB	chr5:49963071-49963619	MCF-7	breast:	n/a	n/a
45	CEBPB	chr5:49963029-49963481	MCF-7	breast:	n/a	n/a
46	CEBPB	chr5:49963280-49963440	K562	blood:	n/a	n/a
47	CEBPB	chr5:49963037-49963612	ECC-1	luminal epithelium:	n/a	n/a
48	CEBPB	chr5:49962793-49963570	Hela-S3	cervix:	n/a	n/a
49	CEBPB	chr5:49963169-49963482	ECC-1	luminal epithelium:	n/a	n/a
50	CEBPB	chr5:49963185-49963549	A549	lung:	n/a	n/a

(count:855 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:49962729-49962779	BE2_C	brain:	n/a
2	chr5:49962729-49962779	BE2_C	brain:	n/a
3	chr5:49962507-49962557	NB4	blood:	n/a
4	chr5:49963156-49963206	MCF10A-Er-Src	breast:	n/a
5	chr5:49964166-49964216	U87	brain:	n/a
6	chr5:49963156-49963206	GM06990	blood:	n/a
7	chr5:49963156-49963206	K562	blood:	n/a
8	chr5:49962954-49963004	ProgFib	skin:	n/a
9	chr5:49961846-49961896	PFSK-1	brain:	n/a
10	chr5:49966777-49966827	AG09319	gingival:	n/a
11	chr5:49961381-49961431	H1-hESC	embryonic stem cell:	embryo
12	chr5:49963580-49963630	GM12891	blood:	n/a
13	chr5:49962729-49962779	BJ	skin:	n/a
14	chr5:49962977-49963027	GM12878	blood:	n/a
15	chr5:49961846-49961896	HPAEpiC	pulmonary alveolar:	n/a
16	chr5:49962613-49962663	GM06990	blood:	n/a
17	chr5:49966777-49966827	HRE	kidney:	n/a
18	chr5:49961846-49961896	Hepatocyte	liver:	n/a
19	chr5:49963801-49963851	PANC-1	pancreas:	n/a
20	chr5:49961846-49961896	BJ	skin:	n/a
21	chr5:49962977-49963027	HMEC	breast:	n/a
22	chr5:49961846-49961896	NB4	blood:	n/a
23	chr5:49963801-49963851	GM06990	blood:	n/a
24	chr5:49962613-49962663	Jurkat	blood:	n/a
25	chr5:49962509-49962559	HL-60	blood:	n/a
26	chr5:49961381-49961431	AG09309	skin:	n/a
27	chr5:49962507-49962557	AG09309	skin:	n/a
28	chr5:49963156-49963206	HPAEpiC	pulmonary alveolar:	n/a
29	chr5:49963801-49963851	NHDF-neo	bronchial:	n/a
30	chr5:49961381-49961431	AG04449	skin:	fetal
31	chr5:49963156-49963206	HCF	heart:	n/a
32	chr5:49961846-49961896	RPTEC	kidney:	n/a
33	chr5:49961381-49961431	Hela-S3	cervix:	n/a
34	chr5:49963801-49963851	MCF-7	breast:	n/a
35	chr5:49964166-49964216	NB4	blood:	n/a
36	chr5:49962954-49963004	Hela-S3	cervix:	n/a
37	chr5:49962954-49963004	HEK293	kidney:	embryo
38	chr5:49962613-49962663	HL-60	blood:	n/a
39	chr5:49963580-49963630	PrEC	prostate:	n/a
40	chr5:49963580-49963630	Jurkat	blood:	n/a
41	chr5:49962729-49962779	AG04450	lung:	fetal
42	chr5:49961846-49961896	ProgFib	skin:	n/a
43	chr5:49962954-49963004	AG04450	lung:	fetal
44	chr5:49962977-49963027	IMR90	lung:	fetal
45	chr5:49962613-49962663	CMK	blood:	n/a
46	chr5:49962977-49963027	HIPEpiC	eye:	n/a
47	chr5:49962977-49963027	ECC-1	luminal epithelium:	n/a
48	chr5:49961381-49961431	AG04450	lung:	fetal
49	chr5:49962613-49962663	PrEC	prostate:	n/a
50	chr5:49963580-49963630	AG09319	gingival:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr5:49963990..49965571-chr5:49984249..49987060,2	MCF-7	breast:
2	chr20:9344139..9345018-chr5:49970141..49970936,2	MCF-7	breast:
3	chr5:49966970..49969642-chr5:50045524..50047649,2	MCF-7	breast:
4	chr5:49973996..49976524-chr5:49985360..49987243,2	MCF-7	breast:
5	chr5:49962787..49964612-chr5:49967934..49969609,2	MCF-7	breast:
6	chr5:49965470..49967570-chr5:49976528..49979367,2	MCF-7	breast:
7	chr5:49970649..49973265-chr5:49975299..49977722,2	MCF-7	breast:
8	chr5:49976617..49978344-chr5:49983964..49986828,2	MCF-7	breast:
9	chr5:49979801..49982370-chr5:49986606..49988193,2	MCF-7	breast:
10	chr5:49965470..49967570-chr5:49976528..49979367,2	MCF-7	breast:
11	chr5:49970649..49973265-chr5:49975299..49977722,2	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000271752	TF binding region
PARP8	TF binding region
ENSG00000271752	CpG island
PARP8	CpG island
ENSG00000151883	chromatin interactions

Extended variants
information (count: 735 )
Associated
traits (count: 82 )

Variant overlapped rSNPs/rCNVs (count:735 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs113005760	chr5:49961360-49961361	Weak transcription Enhancers Flanking Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
2	rs552988277	chr5:49961432-49961433	Enhancers Weak transcription Flanking Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
3	rs572897708	chr5:49961495-49961496	Enhancers Weak transcription Flanking Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
4	rs528575920	chr5:49961506-49961507	Enhancers Weak transcription Flanking Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
5	rs545297842	chr5:49961507-49961508	Enhancers Weak transcription Flanking Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
6	rs565197093	chr5:49961581-49961582	Enhancers Weak transcription Flanking Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
7	rs190092544	chr5:49961636-49961637	Bivalent Enhancer Enhancers Active TSS Bivalent/Poised TSS Flanking Active TSS Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
8	rs544763422	chr5:49961673-49961674	Bivalent Enhancer Enhancers Active TSS Bivalent/Poised TSS Flanking Active TSS Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
9	rs534863102	chr5:49961679-49961680	Bivalent Enhancer Enhancers Active TSS Bivalent/Poised TSS Flanking Active TSS Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
10	rs141221352	chr5:49961724-49961725	Bivalent Enhancer Enhancers Active TSS Bivalent/Poised TSS Flanking Active TSS Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
11	rs529831497	chr5:49961822-49961823	Bivalent/Poised TSS Active TSS Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
12	rs546709764	chr5:49961831-49961832	Bivalent/Poised TSS Active TSS Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
13	rs370184319	chr5:49961915-49961916	Bivalent/Poised TSS Active TSS Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
14	rs560238061	chr5:49961922-49961923	Bivalent/Poised TSS Active TSS Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
15	rs200457673	chr5:49961942-49961943	Bivalent/Poised TSS Active TSS Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
16	rs552512337	chr5:49961955-49961956	Bivalent/Poised TSS Active TSS Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
17	rs182740008	chr5:49961982-49961983	Bivalent/Poised TSS Active TSS Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
18	rs557432899	chr5:49961984-49961985	Bivalent/Poised TSS Active TSS Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
19	rs548396119	chr5:49962006-49962007	Active TSS Enhancers Bivalent/Poised TSS Flanking Active TSS Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
20	rs115596628	chr5:49962054-49962055	Active TSS Enhancers Bivalent/Poised TSS Flanking Active TSS Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
21	rs536797897	chr5:49962069-49962070	Active TSS Enhancers Bivalent/Poised TSS Flanking Active TSS Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
22	rs147732631	chr5:49962137-49962138	Active TSS Enhancers Bivalent/Poised TSS Flanking Active TSS Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
23	rs185972727	chr5:49962138-49962139	Active TSS Enhancers Bivalent/Poised TSS Flanking Active TSS Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
24	rs75813288	chr5:49962142-49962143	Active TSS Enhancers Bivalent/Poised TSS Flanking Active TSS Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
25	rs66912405	chr5:49962166-49962167	Active TSS Enhancers Bivalent/Poised TSS Flanking Active TSS Weak transcription	TF binding region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
26	rs78868018	chr5:49962174-49962175	Active TSS Enhancers Bivalent/Poised TSS Flanking Active TSS Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
27	rs62366936	chr5:49962179-49962180	Active TSS Enhancers Bivalent/Poised TSS Flanking Active TSS Weak transcription	TF binding region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs575916226	chr5:49962238-49962239	Active TSS Bivalent/Poised TSS Flanking Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
29	rs116605114	chr5:49962257-49962258	Active TSS Bivalent/Poised TSS Flanking Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
30	rs561599013	chr5:49962304-49962305	Active TSS Bivalent/Poised TSS Flanking Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
31	rs114041400	chr5:49962308-49962309	Active TSS Bivalent/Poised TSS Flanking Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
32	rs574888064	chr5:49962325-49962326	Active TSS Bivalent/Poised TSS Flanking Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
33	rs540374016	chr5:49962354-49962355	Active TSS Bivalent/Poised TSS Flanking Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
34	rs560278149	chr5:49962391-49962392	Active TSS Bivalent/Poised TSS Flanking Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
35	rs147551224	chr5:49962409-49962410	Active TSS Flanking Active TSS Bivalent/Poised TSS	TF binding region	2 gene(s)	Overlapped CNVs	mRNA abundance
36	rs545791317	chr5:49962432-49962433	Active TSS Flanking Active TSS Bivalent/Poised TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
37	rs569523277	chr5:49962515-49962516	Active TSS Flanking Active TSS Bivalent/Poised TSS	TF binding region CpG island	2 gene(s)	Overlapped CNVs	n/a
38	rs550473029	chr5:49962537-49962538	Active TSS Flanking Active TSS Bivalent/Poised TSS	TF binding region CpG island	2 gene(s)	Overlapped CNVs	n/a
39	rs373355771	chr5:49962538-49962539	Active TSS Flanking Active TSS Bivalent/Poised TSS	TF binding region CpG island	2 gene(s)	Overlapped CNVs	n/a
40	rs562314379	chr5:49962556-49962557	Active TSS Flanking Active TSS Bivalent/Poised TSS	TF binding region CpG island	2 gene(s)	Overlapped CNVs	n/a
41	rs531645619	chr5:49962573-49962574	Active TSS Flanking Active TSS Bivalent/Poised TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
42	rs548141298	chr5:49962636-49962637	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island	2 gene(s)	Overlapped CNVs	n/a
43	rs4324624	chr5:49962666-49962667	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs376847175	chr5:49962685-49962686	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region	2 gene(s)	Overlapped CNVs	n/a
45	rs546725286	chr5:49962687-49962688	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region	2 gene(s)	Overlapped CNVs	n/a
46	rs151280834	chr5:49962737-49962738	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island	2 gene(s)	Overlapped CNVs	n/a
47	rs566605770	chr5:49962795-49962796	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region	2 gene(s)	Overlapped CNVs	n/a
48	rs188943275	chr5:49962808-49962809	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region	2 gene(s)	Overlapped CNVs	n/a
49	rs558924820	chr5:49962826-49962827	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region	2 gene(s)	Overlapped CNVs	n/a
50	rs569116015	chr5:49962832-49962833	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:82)

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
Colorectal cancer	21645411	CNVD
Gastric cancer	22152101	CNVD
Oesophago-gastric ulcer	22152101	CNVD
Ovarian cancer	21781307	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Multiple myeloma	17550852	CNVD
Thoracic aortic aneurysm	21092924	CNVD
DNA damage stimulus	22844521	CNVD
DNA repair	22844521	CNVD
Breast cancer	21785460	CNVD
Spinal muscular atrophy	22422766	CNVD
Spinal muscular atrophy	22558076	CNVD
Spinal muscular atrophy	21320981	CNVD
Spinal muscular atrophy	21762474	CNVD
Cancer	16751803	CNVD
Autism	22495311	CNVD
Intellectual disability	22102821	CNVD
Prostate cancer	21965145	CNVD
Cancer	21183584	CNVD
Ovarian cancer	20844748	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Breast cancer	17603634	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Melanoma	18172304	CNVD
Glioma	20126413	CNVD
Non-small cell lung cancer	21829676	CNVD
Breast cancer	22032731	CNVD
Esophageal cancer	20955586	CNVD
Congenital anomalies of the kidney and urinary tract	18694510	CNVD
Breast cancer	17393978	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Acute myeloid leukemia	20729466	CNVD
Cancer	21359685	CNVD
adenomatous polyposis	22470819	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Myelofibrosis	22110671	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
Acute myeloid leukemia	21251322	CNVD
Breast cancer	21364760	CNVD
Oral cancer	21386901	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:875 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:49949800-49961600	Weak transcription	H9 Cell Line	embryonic stem cell
2	chr5:49953000-49961800	Weak transcription	Esophagus	oesophagus
3	chr5:49958800-49961800	Enhancers	Primary monocytes fromperipheralblood	blood
4	chr5:49959200-49961600	Enhancers	Primary neutrophils fromperipheralblood	blood
5	chr5:49959200-49961800	Enhancers	Primary hematopoietic stem cells short term culture	blood
6	chr5:49959400-49961400	Enhancers	Primary T cells from cord blood	blood
7	chr5:49959400-49961400	Enhancers	Primary T killer memory cells from peripheral blood	blood
8	chr5:49959400-49961600	Enhancers	Primary T killer naive cells fromperipheralblood	blood
9	chr5:49959600-49961400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
10	chr5:49959600-49961600	Enhancers	Primary T helper naive cells from peripheral blood	blood
11	chr5:49959600-49961600	Enhancers	Primary T helper cells fromperipheralblood	blood
12	chr5:49959600-49961600	Weak transcription	Brain Inferior Temporal Lobe	brain
13	chr5:49959600-49961800	Weak transcription	Small Intestine	intestine
14	chr5:49959600-49962200	Weak transcription	Left Ventricle	heart
15	chr5:49959800-49962200	Weak transcription	Lung	lung
16	chr5:49959800-49962200	Weak transcription	Spleen	Spleen
17	chr5:49960000-49961600	Enhancers	Primary T helper cells PMA-I stimulated	--
18	chr5:49960000-49961800	Weak transcription	Adipose Nuclei	Adipose
19	chr5:49960000-49961800	Weak transcription	Placenta	Placenta
20	chr5:49960400-49961600	Weak transcription	Fetal Lung	lung
21	chr5:49960400-49961600	Enhancers	Stomach Mucosa	stomach
22	chr5:49960600-49961600	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
23	chr5:49960800-49961400	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
24	chr5:49960800-49961600	Enhancers	Primary T cells fromperipheralblood	blood
25	chr5:49961000-49961400	Enhancers	Primary T regulatory cells fromperipheralblood	blood
26	chr5:49961000-49961400	Enhancers	Duodenum Mucosa	Duodenum
27	chr5:49961000-49961600	Enhancers	Primary B cells from cord blood	blood
28	chr5:49961000-49961600	Enhancers	Primary B cells from peripheral blood	blood
29	chr5:49961000-49961600	Enhancers	Primary hematopoietic stem cells	blood
30	chr5:49961000-49961600	Enhancers	Primary T helper naive cells fromperipheralblood	blood
31	chr5:49961000-49961600	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
32	chr5:49961000-49961600	Enhancers	Brain Substantia Nigra	brain
33	chr5:49961000-49961600	Enhancers	Stomach Smooth Muscle	stomach
34	chr5:49961000-49961800	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
35	chr5:49961000-49961800	Enhancers	Fetal Thymus	thymus
36	chr5:49961000-49961800	Enhancers	Rectal Mucosa Donor 31	rectum
37	chr5:49961000-49961800	Enhancers	Dnd41	blood
38	chr5:49961200-49961600	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
39	chr5:49961200-49961600	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
40	chr5:49961200-49961600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
41	chr5:49961200-49961600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
42	chr5:49961200-49961600	Flanking Active TSS	GM12878-XiMat	blood
43	chr5:49961200-49962000	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
44	chr5:49961200-49962200	Weak transcription	Pancreas	Pancrea
45	chr5:49961400-49961600	Flanking Active TSS	Primary T cells from cord blood	blood
46	chr5:49961400-49961600	Flanking Active TSS	Primary T helper memory cells from peripheral blood 1	blood
47	chr5:49961400-49961600	Enhancers	Brain Anterior Caudate	brain
48	chr5:49961400-49961600	Flanking Active TSS	Duodenum Mucosa	Duodenum
49	chr5:49961400-49961600	Enhancers	NHEK	skin
50	chr5:49961400-49961800	Enhancers	Breast Myoepithelial Primary Cells	Breast

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