Variant report

Variant	nsv881732
Chromosome Location	chr5:61811970-62063366
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1620)
CpG islands
(count:488)
Chromatin interactive
region (count:78)
LncRNA
region (count:12)
Mature miRNA
region (count: 0)
miRNA target
sites (count:1)

(count:1620 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr5:61884567-61884909	HepG2	liver:	n/a	n/a
2	ARID3A	chr5:61948019-61948444	HepG2	liver:	n/a	n/a
3	ARID3A	chr5:61953771-61953952	HepG2	liver:	n/a	n/a
4	ARID3A	chr5:61976936-61977433	HepG2	liver:	n/a	n/a
5	ARID3A	chr5:61834143-61834798	K562	blood:	n/a	n/a
6	ARID3A	chr5:62037767-62038406	HepG2	liver:	n/a	n/a
7	ARID3A	chr5:61896465-61897039	HepG2	liver:	n/a	n/a
8	ARID3A	chr5:61889247-61889447	K562	blood:	n/a	n/a
9	ARID3A	chr5:61881564-61882083	K562	blood:	n/a	n/a
10	ATF1	chr5:61881568-61881851	K562	blood:	n/a	n/a
11	ATF1	chr5:62004400-62004644	K562	blood:	n/a	n/a
12	ATF1	chr5:61834328-61834785	K562	blood:	n/a	n/a
13	ATF2	chr5:61870304-61870858	GM12878	blood:	n/a	n/a
14	ATF3	chr5:62015871-62016064	K562	blood:	n/a	n/a
15	BACH1	chr5:61889249-61889500	K562	blood:	n/a	chr5:61889372-61889386
16	BACH1	chr5:61917202-61917344	K562	blood:	n/a	n/a
17	BACH1	chr5:61823230-61823237	K562	blood:	n/a	n/a
18	BACH1	chr5:61986215-61986345	K562	blood:	n/a	n/a
19	BACH1	chr5:61847461-61847507	K562	blood:	n/a	n/a
20	BACH1	chr5:61865990-61866018	K562	blood:	n/a	n/a
21	BACH1	chr5:61834564-61834771	K562	blood:	n/a	n/a
22	BACH1	chr5:61833258-61833381	K562	blood:	n/a	n/a
23	BATF	chr5:61865376-61865608	GM12878	blood:	n/a	chr5:61865577-61865585
24	BATF	chr5:61870405-61870771	GM12878	blood:	n/a	n/a
25	BATF	chr5:61870477-61870741	GM12878	blood:	n/a	n/a
26	BCL3	chr5:61890237-61890608	GM12878	blood:	n/a	n/a
27	BCL3	chr5:62056284-62056836	GM12878	blood:	n/a	n/a
28	BCLAF1	chr5:61870371-61870825	GM12878	blood:	n/a	n/a
29	BHLHE40	chr5:61945436-61945510	K562	blood:	n/a	n/a
30	BHLHE40	chr5:61872555-61872604	K562	blood:	n/a	n/a
31	BHLHE40	chr5:61927952-61927976	K562	blood:	n/a	n/a
32	BHLHE40	chr5:61889303-61889559	K562	blood:	n/a	n/a
33	BHLHE40	chr5:61884498-61884971	HepG2	liver:	n/a	n/a
34	BHLHE40	chr5:62015797-62016298	GM12878	blood:	n/a	n/a
35	BHLHE40	chr5:61834289-61834768	K562	blood:	n/a	n/a
36	BHLHE40	chr5:61888807-61888814	K562	blood:	n/a	n/a
37	BHLHE40	chr5:62015830-62016143	K562	blood:	n/a	n/a
38	BHLHE40	chr5:61917176-61917369	K562	blood:	n/a	n/a
39	BHLHE40	chr5:62015848-62016138	HepG2	liver:	n/a	n/a
40	BHLHE40	chr5:62058497-62058551	GM12878	blood:	n/a	n/a
41	BHLHE40	chr5:61884632-61884843	HepG2	liver:	n/a	n/a
42	BRCA1	chr5:61968131-61968149	GM12878	blood:	n/a	n/a
43	BRCA1	chr5:61834474-61834740	Hela-S3	cervix:	n/a	n/a
44	CBX3	chr5:61863976-61864361	K562	blood:	n/a	n/a
45	CBX3	chr5:61863983-61864320	K562	blood:	n/a	n/a
46	CBX3	chr5:61834280-61834852	K562	blood:	n/a	n/a
47	CBX3	chr5:62004057-62004283	K562	blood:	n/a	n/a
48	CBX3	chr5:61917097-61917474	K562	blood:	n/a	n/a
49	CCNT2	chr5:61834507-61834787	K562	blood:	n/a	n/a
50	CCNT2	chr5:61876573-61876767	K562	blood:	n/a	n/a

(count:488 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:61874017-61874067	HRE	kidney:	n/a
2	chr5:62014804-62014854	LNCaP	prostate:	n/a
3	chr5:61876634-61876684	HEEpiC	esophagus:	n/a
4	chr5:61890255-61890305	HAEpiC	amniotic membrane:	n/a
5	chr5:61923204-61923254	HCT-116	colon:	n/a
6	chr5:61844855-61844905	Caco-2	colon:	n/a
7	chr5:61923204-61923254	BJ	skin:	n/a
8	chr5:61844855-61844905	NHBE	bronchial:	n/a
9	chr5:61876634-61876684	HCF	heart:	n/a
10	chr5:61874017-61874067	Hepatocyte	liver:	n/a
11	chr5:61844855-61844905	AG09319	gingival:	n/a
12	chr5:61844855-61844905	SK-N-SH	brain:	n/a
13	chr5:61917363-61917413	HCT-116	colon:	n/a
14	chr5:61874017-61874067	HCM	heart:	n/a
15	chr5:61890255-61890305	AoSMC	blood vessel:	n/a
16	chr5:61876634-61876684	GM12891	blood:	n/a
17	chr5:61890255-61890305	GM19239	blood:	n/a
18	chr5:61923204-61923254	IMR90	lung:	fetal
19	chr5:61890255-61890305	HMEC	breast:	n/a
20	chr5:61874017-61874067	GM12891	blood:	n/a
21	chr5:62014804-62014854	SKMC	muscle:	n/a
22	chr5:61874017-61874067	BJ	skin:	n/a
23	chr5:61876634-61876684	IMR90	lung:	fetal
24	chr5:61917363-61917413	AG04450	lung:	fetal
25	chr5:61890255-61890305	SAEC	small airway:	n/a
26	chr5:61923204-61923254	SK-N-MC	brain:	n/a
27	chr5:61818801-61818851	HNPCEpiC	eye:	n/a
28	chr5:62014804-62014854	NHBE	bronchial:	n/a
29	chr5:61890255-61890305	SK-N-MC	brain:	n/a
30	chr5:61890255-61890305	PANC-1	pancreas:	n/a
31	chr5:61923204-61923254	BE2_C	brain:	n/a
32	chr5:61923204-61923254	Jurkat	blood:	n/a
33	chr5:61917363-61917413	HUVEC	blood vessel:	n/a
34	chr5:61818801-61818851	Hepatocyte	liver:	n/a
35	chr5:61923204-61923254	MCF10A-Er-Src	breast:	n/a
36	chr5:61874017-61874067	SK-N-SH	brain:	n/a
37	chr5:61890255-61890305	AG09309	skin:	n/a
38	chr5:62014804-62014854	U87	brain:	n/a
39	chr5:61818801-61818851	MCF10A-Er-Src	breast:	n/a
40	chr5:62014804-62014854	AG09319	gingival:	n/a
41	chr5:61844855-61844905	HUVEC	blood vessel:	n/a
42	chr5:61876634-61876684	HIPEpiC	eye:	n/a
43	chr5:61844855-61844905	HAEpiC	amniotic membrane:	n/a
44	chr5:61844855-61844905	HL-60	blood:	n/a
45	chr5:61917363-61917413	BJ	skin:	n/a
46	chr5:61923204-61923254	H1-hESC	embryonic stem cell:	embryo
47	chr5:61874017-61874067	HNPCEpiC	eye:	n/a
48	chr5:61844855-61844905	HCM	heart:	n/a
49	chr5:61818801-61818851	AG04450	lung:	fetal
50	chr5:61923204-61923254	AG04449	skin:	fetal

(count:78 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr5:61826046..61828158-chr5:61830735..61833492,2	K562	blood:
2	chr5:61897835..61900758-chr5:61901696..61904448,2	K562	blood:
3	chr5:61827589..61829469-chr5:61829575..61831772,2	MCF-7	breast:
4	chr5:61882277..61887456-chr5:61887734..61891517,4	K562	blood:
5	chr5:62036443..62039207-chr5:62041195..62044511,3	K562	blood:
6	chr5:61875725..61878816-chr5:61880010..61882591,3	MCF-7	breast:
7	chr5:62030684..62032945-chr5:62039649..62042488,2	MCF-7	breast:
8	chr5:61886664..61889076-chr5:61892678..61895496,2	MCF-7	breast:
9	chr5:61886779..61891355-chr5:61892416..61896612,4	K562	blood:
10	chr5:61940617..61943358-chr5:61943464..61946144,3	K562	blood:
11	chr5:61909872..61912743-chr5:61916842..61918403,2	MCF-7	breast:
12	chr5:61892474..61895061-chr5:61895378..61897729,2	K562	blood:
13	chr5:61886779..61891355-chr5:61892416..61896612,4	K562	blood:
14	chr5:61822169..61825461-chr5:61826034..61828796,3	K562	blood:
15	chr5:61915873..61918235-chr5:61922517..61925303,2	K562	blood:
16	chr5:61936086..61938123-chr5:61944668..61946794,2	K562	blood:
17	chr5:62018815..62021360-chr5:62022661..62025357,2	K562	blood:
18	chr5:61833161..61835046-chr5:61842892..61845396,3	K562	blood:
19	chr5:61897835..61900758-chr5:61901696..61904448,2	K562	blood:
20	chr5:61872292..61875048-chr5:61884712..61886255,2	K562	blood:
21	chr5:61893060..61895061-chr5:61895378..61897801,2	K562	blood:
22	chr5:62061013..62063521-chr5:62063661..62066191,2	K562	blood:
23	chr5:61513831..61515618-chr5:61821739..61824122,2	K562	blood:
24	chr5:61827589..61829469-chr5:61829575..61831772,2	MCF-7	breast:
25	chr5:61978360..61980328-chr5:61986158..61988132,2	K562	blood:
26	chr5:62018815..62021360-chr5:62022661..62025357,2	K562	blood:
27	chr5:61833675..61836577-chr5:61862911..61865153,3	K562	blood:
28	chr5:61881611..61886681-chr5:61887454..61890458,4	K562	blood:
29	chr5:61915873..61918235-chr5:61922517..61925303,2	K562	blood:
30	chr5:61820977..61823095-chr5:61832322..61835003,2	MCF-7	breast:
31	chr5:61929416..61931059-chr5:61937366..61939285,2	K562	blood:
32	chr5:61905876..61908467-chr5:61910449..61913197,3	K562	blood:
33	chr5:62017098..62019061-chr5:62042354..62044460,2	K562	blood:
34	chr5:62030684..62032945-chr5:62039649..62042488,2	MCF-7	breast:
35	chr5:61898028..61900560-chr5:61910431..61912053,2	MCF-7	breast:
36	chr5:62017098..62019061-chr5:62042354..62044460,2	K562	blood:
37	chr5:61822169..61825461-chr5:61826034..61828796,3	K562	blood:
38	chr5:61925893..61927703-chr5:61935030..61937549,2	K562	blood:
39	chr5:61912906..61915006-chr5:61917150..61920034,2	K562	blood:
40	chr5:61875507..61877206-chr5:61878546..61880725,2	K562	blood:
41	chr5:61886664..61889076-chr5:61892678..61895496,2	MCF-7	breast:
42	chr5:61905876..61908467-chr5:61910449..61913197,3	K562	blood:
43	chr5:61898028..61900560-chr5:61910431..61912053,2	MCF-7	breast:
44	chr5:61875507..61877206-chr5:61878546..61880725,2	K562	blood:
45	chr5:62000604..62002658-chr5:62007528..62009304,2	K562	blood:
46	chr5:61881611..61886681-chr5:61887454..61890458,4	K562	blood:
47	chr5:61925893..61927703-chr5:61935030..61937549,2	K562	blood:
48	chr5:61909872..61912743-chr5:61916842..61918403,2	MCF-7	breast:
49	chr5:62036443..62039207-chr5:62041195..62044511,3	K562	blood:
50	chr5:61882277..61887456-chr5:61887734..61891517,4	K562	blood:

(count:12 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-LRRC70-1	chr5:61887404-61887477	NONHSAT101713
2	lnc-LRRC70-1	chr5:61856523-61856832	NONHSAT101713
3	lnc-IPO11-2	chr5:61963594-61963682	NONHSAT101718
4	lnc-IPO11-2	chr5:61957255-61957780	NONHSAT101718
5	lnc-DIMT1-3	chr5:61938348-61938891	NONHSAT101717
6	lnc-LRRC70-1	chr5:61874664-61874762	NONHSAT101716
7	lnc-LRRC70-1	chr5:61876281-61877269	NONHSAT101716
8	lnc-DIMT1-1	chr5:61857686-61858043	NONHSAT101714
9	lnc-DIMT1-2	chr5:61871778-61872098	NONHSAT101715
10	lnc-DIMT1-3	chr5:61937940-61938054	NONHSAT101717
11	lnc-LRRC70-1	chr5:61875228-61875310	NONHSAT101716
12	lnc-LRRC70-1	chr5:61856963-61857084	NONHSAT101713

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	IPO11	hsa-miR-16-5p	chr5:61923396-61923417

Variant related genes	Relation type
ENSG00000241991	TF binding region
LRRC70	TF binding region
ENSG00000268942	TF binding region
IPO11	TF binding region
ENSG00000240436	TF binding region
ENSG00000241991	CpG island
LRRC70	CpG island
ENSG00000268942	CpG island
IPO11	CpG island
ENSG00000240436	CpG island
ENSG00000186105	chromatin interactions
ENSG00000086200	chromatin interactions

Extended variants
information (count: 7810 )
Associated
traits (count: 96 )

Variant overlapped rSNPs/rCNVs (count:7810 , 50 per page) page: 1 2 3 4 5 6 7 ... 157

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6875068	chr5:61811970-61811971	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs185544190	chr5:61812065-61812066	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs368698584	chr5:61812070-61812071	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs557031870	chr5:61812107-61812108	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs141110252	chr5:61812119-61812120	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs571525280	chr5:61812147-61812148	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs150278982	chr5:61812151-61812152	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs558594944	chr5:61812158-61812159	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs32189	chr5:61812183-61812184	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs540946126	chr5:61812232-61812233	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs554784059	chr5:61812240-61812241	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs574677403	chr5:61812276-61812277	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs543591090	chr5:61812368-61812369	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs190402023	chr5:61812401-61812402	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs532157361	chr5:61812412-61812413	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs542549673	chr5:61812414-61812415	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs181755492	chr5:61812446-61812447	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs559060719	chr5:61812456-61812457	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs186784431	chr5:61812499-61812500	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs540142459	chr5:61812521-61812522	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs190198410	chr5:61812527-61812528	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs565862909	chr5:61812537-61812538	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs538495877	chr5:61812566-61812567	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs531413197	chr5:61812592-61812593	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs181083328	chr5:61812626-61812627	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs185216613	chr5:61812640-61812641	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs570576523	chr5:61812641-61812642	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs552323175	chr5:61812681-61812682	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs563852129	chr5:61812683-61812684	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs539470711	chr5:61812716-61812717	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs189641794	chr5:61812761-61812762	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs566738686	chr5:61812792-61812793	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs371560272	chr5:61812802-61812803	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs183436645	chr5:61812850-61812851	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs111406049	chr5:61812853-61812854	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs528561254	chr5:61812854-61812855	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs574689448	chr5:61812885-61812886	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs543605175	chr5:61812886-61812887	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs557110234	chr5:61812892-61812893	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs577038452	chr5:61812894-61812895	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs549512378	chr5:61812938-61812939	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs559339339	chr5:61812966-61812967	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs34562047	chr5:61812979-61812980	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs138401054	chr5:61812980-61812981	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs372957565	chr5:61812982-61812983	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs71617437	chr5:61812994-61812995	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs71590889	chr5:61813004-61813005	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs200717906	chr5:61813025-61813026	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs75156068	chr5:61813034-61813035	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs547706034	chr5:61813045-61813046	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:96)

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
Intellectual disability	22102821	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
Prostate cancer	21965145	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
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
Acute myeloid leukemia	20729466	CNVD
Acute myeloid leukemia	21251322	CNVD
Oral cancer	21386901	CNVD
Bladder cancer	21909424	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Barrett''s syndrome	19417022	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Breast cancer	17133270	CNVD
Breast cancer	19602461	CNVD
Renal cell carcinoma	18194544	CNVD
abnormal development	18461090	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Retinoblastoma	22278416	CNVD
Bipolar disorder	18458673	CNVD
Thyroid cancer	19087340	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	21364760	CNVD
Colorectal cancer	16774939	CNVD
Myelofibrosis	22110671	CNVD
Neuroticism	17667963	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:2385 , 50 per page) page: 1 2 3 4 5 6 7 ... 48

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:61728800-61838200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
2	chr5:61730000-61834200	Weak transcription	Gastric	stomach
3	chr5:61739200-61862800	Weak transcription	Brain Substantia Nigra	brain
4	chr5:61744800-61838600	Weak transcription	Colonic Mucosa	Colon
5	chr5:61748000-61862800	Weak transcription	Right Ventricle	heart
6	chr5:61758800-61890000	Weak transcription	Small Intestine	intestine
7	chr5:61759000-61834200	Weak transcription	Esophagus	oesophagus
8	chr5:61760800-61847200	Weak transcription	Rectal Smooth Muscle	rectum
9	chr5:61764000-61833800	Weak transcription	Fetal Brain Female	brain
10	chr5:61764000-61858200	Weak transcription	Placenta	Placenta
11	chr5:61764200-61818000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
12	chr5:61764200-61821200	Weak transcription	Aorta	Aorta
13	chr5:61764200-61826600	Weak transcription	Brain Hippocampus Middle	brain
14	chr5:61764200-61827000	Weak transcription	Thymus	Thymus
15	chr5:61764200-61830000	Weak transcription	Brain Angular Gyrus	brain
16	chr5:61764200-61895800	Weak transcription	Pancreas	Pancrea
17	chr5:61766200-61849800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
18	chr5:61771200-61864800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
19	chr5:61771400-61863000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
20	chr5:61772200-61850800	Weak transcription	HSMMtube	muscle
21	chr5:61772600-61842000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
22	chr5:61773600-61813400	Weak transcription	NHDF-Ad	bronchial
23	chr5:61774200-61827000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
24	chr5:61775200-61829200	Weak transcription	Brain Germinal Matrix	brain
25	chr5:61781600-61867600	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
26	chr5:61787200-61836000	Weak transcription	Colon Smooth Muscle	Colon
27	chr5:61787400-61818600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
28	chr5:61787400-61829000	Weak transcription	Brain Anterior Caudate	brain
29	chr5:61787400-61866800	Weak transcription	Skeletal Muscle Male	skeletal muscle
30	chr5:61788800-61827000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
31	chr5:61789400-61835400	Weak transcription	Fetal Brain Male	brain
32	chr5:61792600-61826800	Weak transcription	Hela-S3	cervix
33	chr5:61793200-61813200	Weak transcription	Fetal Thymus	thymus
34	chr5:61793600-61818600	Weak transcription	H1 Cell Line	embryonic stem cell
35	chr5:61793600-61905000	Weak transcription	NHEK	skin
36	chr5:61795000-61834000	Weak transcription	Ovary	ovary
37	chr5:61795200-61850600	Weak transcription	Fetal Intestine Small	intestine
38	chr5:61795800-61814800	Weak transcription	Primary hematopoietic stem cells	blood
39	chr5:61795800-61826600	Weak transcription	Skeletal Muscle Female	skeletal muscle
40	chr5:61796400-61822000	Weak transcription	Rectal Mucosa Donor 29	rectum
41	chr5:61796400-61826400	Weak transcription	Stomach Smooth Muscle	stomach
42	chr5:61796600-61813000	Weak transcription	Fetal Stomach	stomach
43	chr5:61796600-61827000	Weak transcription	Fetal Muscle Leg	muscle
44	chr5:61796600-61866600	Weak transcription	Osteobl	bone
45	chr5:61796800-61815600	Weak transcription	Left Ventricle	heart
46	chr5:61796800-61825800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
47	chr5:61796800-61899000	Weak transcription	Rectal Mucosa Donor 31	rectum
48	chr5:61797000-61813200	Weak transcription	Brain Inferior Temporal Lobe	brain
49	chr5:61797000-61815400	Weak transcription	Cortex derived primary cultured neurospheres	brain
50	chr5:61797000-61825600	Weak transcription	HepG2	liver

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