Variant report

Variant	nsv830300
Chromosome Location	chr5:54056300-54257344
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2808)
CpG islands
(count:1466)
Chromatin interactive
region (count:86)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2808 , 50 per page) page: 1 2 3 4 5 6 7 ... 57

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr5:54163171-54163635	K562	blood:	n/a	n/a
2	ARID3A	chr5:54141069-54141336	HepG2	liver:	n/a	n/a
3	ARID3A	chr5:54240181-54240429	K562	blood:	n/a	chr5:54240308-54240324
4	ARID3A	chr5:54081457-54081768	K562	blood:	n/a	n/a
5	ARID3A	chr5:54062620-54062957	K562	blood:	n/a	n/a
6	ARID3A	chr5:54163180-54163404	HepG2	liver:	n/a	n/a
7	ARID3A	chr5:54240127-54240428	HepG2	liver:	n/a	chr5:54240308-54240324
8	ATF1	chr5:54095291-54095307	K562	blood:	n/a	n/a
9	ATF1	chr5:54240049-54240331	K562	blood:	n/a	n/a
10	ATF1	chr5:54081478-54082382	K562	blood:	n/a	n/a
11	ATF1	chr5:54188412-54188612	K562	blood:	n/a	n/a
12	ATF2	chr5:54164326-54164643	GM12878	blood:	n/a	n/a
13	ATF2	chr5:54198506-54199048	GM12878	blood:	n/a	n/a
14	ATF2	chr5:54164266-54164685	GM12878	blood:	n/a	n/a
15	ATF2	chr5:54198533-54198986	GM12878	blood:	n/a	n/a
16	ATF3	chr5:54179196-54179602	H1-hESC	embryonic stem cell:	n/a	chr5:54179411-54179431 chr5:54179447-54179456
17	ATF3	chr5:54179296-54179548	K562	blood:	n/a	chr5:54179411-54179431 chr5:54179447-54179456
18	ATF3	chr5:54179214-54179669	H1-hESC	embryonic stem cell:	n/a	chr5:54179411-54179431 chr5:54179447-54179456
19	BACH1	chr5:54228762-54228850	H1-hESC	embryonic stem cell:	n/a	n/a
20	BACH1	chr5:54201807-54201837	K562	blood:	n/a	n/a
21	BACH1	chr5:54095442-54095467	K562	blood:	n/a	n/a
22	BATF	chr5:54089964-54090196	GM12878	blood:	n/a	n/a
23	BATF	chr5:54198619-54199016	GM12878	blood:	n/a	n/a
24	BATF	chr5:54198532-54199194	GM12878	blood:	n/a	n/a
25	BATF	chr5:54164293-54164657	GM12878	blood:	n/a	n/a
26	BATF	chr5:54164217-54164685	GM12878	blood:	n/a	n/a
27	BCL11A	chr5:54164314-54164520	GM12878	blood:	n/a	n/a
28	BCL11A	chr5:54081995-54082281	GM12878	blood:	n/a	chr5:54082188-54082195
29	BCL11A	chr5:54198560-54199063	GM12878	blood:	n/a	n/a
30	BCL11A	chr5:54164196-54164719	GM12878	blood:	n/a	n/a
31	BCL3	chr5:54198590-54198945	GM12878	blood:	n/a	n/a
32	BCLAF1	chr5:54198526-54199057	GM12878	blood:	n/a	n/a
33	BCLAF1	chr5:54198542-54198991	GM12878	blood:	n/a	n/a
34	BHLHE40	chr5:54198600-54199018	GM12878	blood:	n/a	n/a
35	BHLHE40	chr5:54158004-54158136	K562	blood:	n/a	n/a
36	BHLHE40	chr5:54070898-54070984	K562	blood:	n/a	n/a
37	BHLHE40	chr5:54082143-54082487	GM12878	blood:	n/a	n/a
38	BHLHE40	chr5:54081473-54082749	K562	blood:	n/a	n/a
39	BHLHE40	chr5:54117988-54118047	K562	blood:	n/a	n/a
40	BHLHE40	chr5:54141030-54141280	GM12878	blood:	n/a	n/a
41	BHLHE40	chr5:54201990-54201992	HepG2	liver:	n/a	n/a
42	BHLHE40	chr5:54179239-54179609	K562	blood:	n/a	chr5:54179421-54179430 chr5:54179422-54179431 chr5:54179422-54179431 chr5:54179420-54179433
43	BRCA1	chr5:54185729-54186121	Hela-S3	cervix:	n/a	chr5:54186019-54186026
44	BRCA1	chr5:54206194-54206208	HepG2	liver:	n/a	n/a
45	BRCA1	chr5:54180821-54180901	Hela-S3	cervix:	n/a	n/a
46	BRCA1	chr5:54103286-54103657	Hela-S3	cervix:	n/a	n/a
47	BRCA1	chr5:54170238-54170757	Hela-S3	cervix:	n/a	n/a
48	CBX3	chr5:54081449-54081952	K562	blood:	n/a	n/a
49	CBX3	chr5:54082002-54082503	K562	blood:	n/a	n/a
50	CCNT2	chr5:54082048-54082434	K562	blood:	n/a	chr5:54082185-54082205

(count:1466 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:54081633-54081683	MCF-7	breast:	n/a
2	chr5:54162153-54162203	HEEpiC	esophagus:	n/a
3	chr5:54081633-54081683	MCF-7	breast:	n/a
4	chr5:54162153-54162203	HEEpiC	esophagus:	n/a
5	chr5:54162153-54162203	AoSMC	blood vessel:	n/a
6	chr5:54179305-54179355	HMEC	breast:	n/a
7	chr5:54117761-54117811	MCF10A-Er-Src	breast:	n/a
8	chr5:54177306-54177356	HRE	kidney:	n/a
9	chr5:54179671-54179721	H1-hESC	embryonic stem cell:	embryo
10	chr5:54179570-54179620	NB4	blood:	n/a
11	chr5:54180079-54180129	GM19239	blood:	n/a
12	chr5:54179305-54179355	HCT-116	colon:	n/a
13	chr5:54131694-54131744	RPTEC	kidney:	n/a
14	chr5:54185940-54185990	HCT-116	colon:	n/a
15	chr5:54140068-54140118	ovcar-3	ovarian:	n/a
16	chr5:54179537-54179587	SK-N-MC	brain:	n/a
17	chr5:54133279-54133329	PrEC	prostate:	n/a
18	chr5:54179671-54179721	NB4	blood:	n/a
19	chr5:54180254-54180304	SKMC	muscle:	n/a
20	chr5:54173814-54173864	PFSK-1	brain:	n/a
21	chr5:54183619-54183669	NB4	blood:	n/a
22	chr5:54117761-54117811	AoSMC	blood vessel:	n/a
23	chr5:54179537-54179587	HCM	heart:	n/a
24	chr5:54081633-54081683	HCM	heart:	n/a
25	chr5:54179671-54179721	GM19239	blood:	n/a
26	chr5:54183619-54183669	Caco-2	colon:	n/a
27	chr5:54162153-54162203	AG10803	skin:	n/a
28	chr5:54183619-54183669	GM12878	blood:	n/a
29	chr5:54140068-54140118	NHBE	bronchial:	n/a
30	chr5:54180079-54180129	HEEpiC	esophagus:	n/a
31	chr5:54117761-54117811	GM06990	blood:	n/a
32	chr5:54179305-54179355	HepG2	liver:	n/a
33	chr5:54128677-54128727	PrEC	prostate:	n/a
34	chr5:54162153-54162203	HepG2	liver:	n/a
35	chr5:54173814-54173864	AG10803	skin:	n/a
36	chr5:54206061-54206111	SK-N-MC	brain:	n/a
37	chr5:54131694-54131744	HCM	heart:	n/a
38	chr5:54180254-54180304	GM12878	blood:	n/a
39	chr5:54179671-54179721	NHBE	bronchial:	n/a
40	chr5:54162153-54162203	GM12892	blood:	n/a
41	chr5:54131694-54131744	U87	brain:	n/a
42	chr5:54206061-54206111	HRCEpiC	kidney:	n/a
43	chr5:54128677-54128727	HUVEC	blood vessel:	n/a
44	chr5:54180170-54180220	NHBE	bronchial:	n/a
45	chr5:54157713-54157763	PrEC	prostate:	n/a
46	chr5:54140068-54140118	HCT-116	colon:	n/a
47	chr5:54179537-54179587	AG09309	skin:	n/a
48	chr5:54179537-54179587	K562	blood:	n/a
49	chr5:54179671-54179721	SK-N-MC	brain:	n/a
50	chr5:54185940-54185990	NH-A	brain:	n/a

(count:86 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr5:54200958..54202481-chr5:54231844..54234321,2	MCF-7	breast:
2	chr5:54187867..54189823-chr5:54194606..54196812,2	K562	blood:
3	chr5:54122100..54123880-chr5:54124518..54126459,2	MCF-7	breast:
4	chr5:53809805..53810607-chr5:54163206..54163801,2	MCF-7	breast:
5	chr5:54036001..54038527-chr5:54062839..54065440,2	MCF-7	breast:
6	chr5:54201807..54203525-chr5:54204934..54206969,2	K562	blood:
7	chr5:53813072..53814349-chr5:54064617..54065503,4	MCF-7	breast:
8	chr5:53813533..53814116-chr5:54191276..54191789,2	MCF-7	breast:
9	chr5:54233030..54235046-chr5:54238189..54240308,2	K562	blood:
10	chr5:54147700..54150094-chr5:54150454..54152173,2	MCF-7	breast:
11	chr5:54239886..54240728-chr5:54255208..54255750,2	MCF-7	breast:
12	chr5:54224711..54226545-chr5:54227369..54230054,2	K562	blood:
13	chr5:54158673..54160817-chr5:54181128..54182793,2	K562	blood:
14	chr5:54131587..54134276-chr5:54135808..54138723,2	K562	blood:
15	chr5:54141228..54143207-chr5:54145045..54147892,2	K562	blood:
16	chr5:54224711..54226545-chr5:54227369..54230054,2	K562	blood:
17	chr5:54201538..54202383-chr5:54442173..54442949,2	MCF-7	breast:
18	chr5:54123243..54126071-chr5:54126953..54129428,2	K562	blood:
19	chr5:54187867..54189823-chr5:54194606..54196812,2	K562	blood:
20	chr5:54240236..54240755-chr5:54442413..54442981,2	K562	blood:
21	chr5:53813794..53815703-chr5:54138497..54141381,2	K562	blood:
22	chr5:53809845..53810748-chr5:54141094..54141605,2	MCF-7	breast:
23	chr5:54061560..54063270-chr5:54063643..54065154,2	K562	blood:
24	chr5:53812974..53814247-chr5:54140692..54141615,7	MCF-7	breast:
25	chr5:54193608..54196298-chr5:54200026..54202116,2	K562	blood:
26	chr5:54061560..54063270-chr5:54063643..54065154,2	K562	blood:
27	chr5:53811747..53814242-chr5:54144763..54147305,2	MCF-7	breast:
28	chr11:130183938..130184879-chr5:54175807..54176307,3	Hela-S3	cervix:
29	chr5:54122100..54123880-chr5:54124518..54126459,2	MCF-7	breast:
30	chr5:54200958..54202481-chr5:54231844..54234321,2	MCF-7	breast:
31	chr5:54131587..54134276-chr5:54135808..54138723,2	K562	blood:
32	chr5:54233030..54235046-chr5:54238189..54240308,2	K562	blood:
33	chr5:54146367..54148886-chr5:54162857..54164996,2	K562	blood:
34	chr5:53813350..53815474-chr5:54061824..54064648,2	MCF-7	breast:
35	chr5:54066799..54068824-chr5:54069202..54071627,2	K562	blood:
36	chr5:54049724..54052539-chr5:54057510..54059343,2	K562	blood:
37	chr5:54053223..54055714-chr5:54058237..54060813,3	K562	blood:
38	chr5:54240119..54240626-chr5:54442148..54443056,2	MCF-7	breast:
39	chr5:54058549..54060576-chr5:54060806..54063597,3	K562	blood:
40	chr5:53813063..53813889-chr5:54199937..54200836,3	K562	blood:
41	chr5:54013909..54016441-chr5:54127667..54129605,2	K562	blood:
42	chr5:54193608..54196298-chr5:54200026..54202116,2	K562	blood:
43	chr5:54201140..54202428-chr5:54255300..54256152,3	MCF-7	breast:
44	chr5:54201490..54202443-chr5:54441779..54443043,5	K562	blood:
45	chr5:53719508..53722499-chr5:54137600..54140313,3	K562	blood:
46	chr5:54240219..54240748-chr5:54455263..54456074,2	MCF-7	breast:
47	chr5:53812465..53813906-chr5:54162875..54163886,10	K562	blood:
48	chr5:54238679..54239586-chr5:54442120..54443036,2	MCF-7	breast:
49	chr5:54123243..54126071-chr5:54126953..54129428,2	K562	blood:
50	chr5:54200140..54200747-chr5:54455224..54456168,2	MCF-7	breast:

(count:5 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GZMK-3	chr5:54153100-54154319	NONHSAT101457
2	lnc-GZMK-3	chr5:54198880-54199047	NONHSAT101456
3	lnc-RP11-45H22.3.1-2	chr5:54162396-54162890	NONHSAT101458
4	lnc-GZMK-3	chr5:54152968-54153294	NONHSAT101456
5	lnc-GZMK-3	chr5:54162398-54162859	NONHSAT101456

No data

Variant related genes	Relation type
ENSG00000221073	TF binding region
ENSG00000226810	TF binding region
ENSG00000232517	TF binding region
ENSG00000249843	TF binding region
ENSG00000249016	TF binding region
ENSG00000221073	CpG island
ENSG00000226810	CpG island
ENSG00000232517	CpG island
ENSG00000249843	CpG island
ENSG00000249016	CpG island
ENSG00000178996	chromatin interactions
ENSG00000196323	chromatin interactions
ENSG00000249843	chromatin interactions
ENSG00000164294	chromatin interactions
ENSG00000221073	chromatin interactions
ENSG00000175309	chromatin interactions

Extended variants
information (count: 6490 )
Associated
traits (count: 92 )

Variant overlapped rSNPs/rCNVs (count:6490 , 50 per page) page: 1 2 3 4 5 6 7 ... 130

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs563706485	chr5:54056316-54056317	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
2	rs183054074	chr5:54056318-54056319	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs546106707	chr5:54056332-54056333	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs564402283	chr5:54056348-54056349	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs146537462	chr5:54056376-54056377	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs369094147	chr5:54056378-54056379	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs188010483	chr5:54056382-54056383	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs532233200	chr5:54056430-54056431	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs150682158	chr5:54056438-54056439	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs113728147	chr5:54056469-54056470	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs62354975	chr5:54056472-54056473	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs80019159	chr5:54056473-54056474	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs79707430	chr5:54056481-54056482	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs537202020	chr5:54056482-54056483	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs377355609	chr5:54056483-54056484	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs183194515	chr5:54056494-54056495	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs116840264	chr5:54056499-54056500	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs114509401	chr5:54056527-54056528	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs79242882	chr5:54056540-54056541	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs7710436	chr5:54056541-54056542	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs145722218	chr5:54056652-54056653	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs556981675	chr5:54056655-54056656	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs575761860	chr5:54056685-54056686	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs374318545	chr5:54056710-54056711	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs75229880	chr5:54056770-54056771	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs187803647	chr5:54056778-54056779	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs7447858	chr5:54056796-54056797	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs192623930	chr5:54056809-54056810	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs184971098	chr5:54056819-54056820	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs148529406	chr5:54056849-54056850	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs540265994	chr5:54056856-54056857	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs561913443	chr5:54056875-54056876	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs529259582	chr5:54056878-54056879	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs144259906	chr5:54056918-54056919	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs146584708	chr5:54056962-54056963	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs562954615	chr5:54056979-54056980	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs186680176	chr5:54056985-54056986	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs140317650	chr5:54057049-54057050	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs370239593	chr5:54057054-54057055	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs145464008	chr5:54057059-54057060	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs192338993	chr5:54057088-54057089	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs546842449	chr5:54057096-54057097	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs567976102	chr5:54057109-54057110	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs184721579	chr5:54057116-54057117	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs189764549	chr5:54057142-54057143	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs556786109	chr5:54057189-54057190	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs151007984	chr5:54057232-54057233	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs539687469	chr5:54057239-54057240	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs557916826	chr5:54057249-54057250	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs573230896	chr5:54057264-54057265	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:92)

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
Cancer	21359685	CNVD
adenomatous polyposis	22470819	CNVD
Acute myeloid leukemia	20729466	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
Lung cancer	18438408	CNVD
Urothelial carcinoma	21177765	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	21364760	CNVD
Oral cancer	21386901	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Bladder cancer	21909424	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Barrett''s syndrome	19417022	CNVD
small cell lung cancer	20016488	CNVD
Myelofibrosis	22110671	CNVD
Lung cancer	21911935	CNVD
Breast cancer	17133270	CNVD
Breast cancer	19602461	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Renal cell carcinoma	18194544	CNVD
abnormal development	18461090	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:1618 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:54049200-54057000	Weak transcription	Fetal Heart	heart
2	chr5:54049400-54056400	Weak transcription	Left Ventricle	heart
3	chr5:54052200-54059800	Weak transcription	Fetal Muscle Leg	muscle
4	chr5:54052600-54058600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
5	chr5:54052600-54058800	Enhancers	NHDF-Ad	bronchial
6	chr5:54053200-54057000	Weak transcription	Ovary	ovary
7	chr5:54053800-54056600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
8	chr5:54054400-54056600	Weak transcription	NH-A	brain
9	chr5:54055000-54057200	Enhancers	Primary monocytes fromperipheralblood	blood
10	chr5:54055000-54058400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
11	chr5:54055000-54058600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
12	chr5:54055200-54056800	Enhancers	Osteobl	bone
13	chr5:54055200-54057200	Enhancers	Aorta	Aorta
14	chr5:54055200-54058600	Enhancers	NHLF	lung
15	chr5:54055400-54058600	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
16	chr5:54055400-54061000	Weak transcription	Pancreas	Pancrea
17	chr5:54055600-54059600	Weak transcription	Primary B cells from cord blood	blood
18	chr5:54056000-54056600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
19	chr5:54056000-54056800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
20	chr5:54056000-54057200	Enhancers	Brain Hippocampus Middle	brain
21	chr5:54056000-54057400	Enhancers	HMEC	breast
22	chr5:54056000-54057600	Weak transcription	Right Atrium	heart
23	chr5:54056000-54057800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
24	chr5:54056000-54057800	Enhancers	HSMM	muscle
25	chr5:54056000-54058400	Enhancers	HSMMtube	muscle
26	chr5:54056200-54056600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
27	chr5:54056200-54057200	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
28	chr5:54056200-54057800	Enhancers	Muscle Satellite Cultured Cells	--
29	chr5:54056400-54057600	Enhancers	Adipose Nuclei	Adipose
30	chr5:54056400-54057600	Enhancers	HUVEC	blood vessel
31	chr5:54056400-54057800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
32	chr5:54056400-54057800	Enhancers	Left Ventricle	heart
33	chr5:54056600-54056800	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
34	chr5:54056600-54057400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
35	chr5:54056600-54057400	Enhancers	Hela-S3	cervix
36	chr5:54056600-54057800	Enhancers	NH-A	brain
37	chr5:54056600-54060000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
38	chr5:54056800-54057000	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
39	chr5:54056800-54057000	Flanking Active TSS	Osteobl	bone
40	chr5:54056800-54057600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
41	chr5:54056800-54057800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
42	chr5:54057000-54057200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
43	chr5:54057000-54057200	Enhancers	Osteobl	bone
44	chr5:54057000-54057400	Enhancers	Fetal Kidney	kidney
45	chr5:54057000-54057600	Enhancers	Fetal Heart	heart
46	chr5:54057000-54057800	Enhancers	Ovary	ovary
47	chr5:54057200-54057400	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
48	chr5:54057200-54057400	Flanking Active TSS	Osteobl	bone
49	chr5:54057200-54057600	Weak transcription	Aorta	Aorta
50	chr5:54057200-54057800	Enhancers	Monocytes-CD14+_RO01746	blood

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