Variant report

Variant	nsv830412
Chromosome Location	chr5:96427305-96606619
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2092)
CpG islands
(count:1347)
Chromatin interactive
region (count:93)
LncRNA
region (count:7)
Mature miRNA
region (count: 0)
miRNA target
sites (count:2)

(count:2092 , 50 per page) page: 1 2 3 4 5 6 7 ... 42

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr5:96517984-96519784	HepG2	liver:	n/a	n/a
2	ARID3A	chr5:96518910-96519735	K562	blood:	n/a	n/a
3	ARID3A	chr5:96517679-96517912	K562	blood:	n/a	n/a
4	ARID3A	chr5:96559836-96560263	HepG2	liver:	n/a	n/a
5	ATF1	chr5:96465539-96465890	K562	blood:	n/a	n/a
6	ATF1	chr5:96463534-96463724	K562	blood:	n/a	n/a
7	ATF1	chr5:96466940-96467134	K562	blood:	n/a	n/a
8	ATF1	chr5:96566806-96567076	K562	blood:	n/a	n/a
9	ATF1	chr5:96518777-96519693	K562	blood:	n/a	n/a
10	ATF2	chr5:96518622-96519567	H1-hESC	embryonic stem cell:	n/a	n/a
11	ATF2	chr5:96503022-96503427	GM12878	blood:	n/a	n/a
12	ATF2	chr5:96470286-96470816	H1-hESC	embryonic stem cell:	n/a	n/a
13	ATF2	chr5:96518742-96519762	GM12878	blood:	n/a	n/a
14	ATF2	chr5:96518562-96519502	GM12878	blood:	n/a	n/a
15	ATF2	chr5:96503064-96503603	GM12878	blood:	n/a	n/a
16	ATF2	chr5:96430546-96431435	GM12878	blood:	n/a	n/a
17	ATF2	chr5:96518721-96519407	H1-hESC	embryonic stem cell:	n/a	n/a
18	ATF2	chr5:96430604-96431433	GM12878	blood:	n/a	n/a
19	ATF3	chr5:96485448-96485735	K562	blood:	n/a	n/a
20	ATF3	chr5:96518727-96519094	K562	blood:	n/a	n/a
21	ATF3	chr5:96518763-96519118	H1-hESC	embryonic stem cell:	n/a	n/a
22	ATF3	chr5:96518699-96519160	H1-hESC	embryonic stem cell:	n/a	n/a
23	ATF3	chr5:96518726-96519630	A549	lung:	n/a	n/a
24	ATF3	chr5:96518734-96519068	HepG2	liver:	n/a	n/a
25	ATF3	chr5:96518715-96519226	GM12878	blood:	n/a	n/a
26	ATF3	chr5:96518825-96519741	A549	lung:	n/a	n/a
27	BACH1	chr5:96441064-96441157	K562	blood:	n/a	n/a
28	BACH1	chr5:96518703-96519565	K562	blood:	n/a	n/a
29	BACH1	chr5:96600161-96600267	H1-hESC	embryonic stem cell:	n/a	n/a
30	BACH1	chr5:96514726-96514765	K562	blood:	n/a	n/a
31	BATF	chr5:96528640-96528915	GM12878	blood:	n/a	n/a
32	BATF	chr5:96430639-96431326	GM12878	blood:	n/a	chr5:96430968-96430978 chr5:96430967-96430978 chr5:96430947-96430958
33	BATF	chr5:96503162-96503595	GM12878	blood:	n/a	chr5:96503383-96503394
34	BATF	chr5:96430694-96431298	GM12878	blood:	n/a	chr5:96430968-96430978 chr5:96430967-96430978 chr5:96430947-96430958
35	BATF	chr5:96503177-96503536	GM12878	blood:	n/a	chr5:96503383-96503394
36	BCL11A	chr5:96470502-96470707	H1-hESC	embryonic stem cell:	n/a	n/a
37	BCL11A	chr5:96430751-96431093	GM12878	blood:	n/a	chr5:96430902-96430911
38	BCL11A	chr5:96470396-96470707	H1-hESC	embryonic stem cell:	n/a	n/a
39	BCL11A	chr5:96528575-96528962	GM12878	blood:	n/a	n/a
40	BCL11A	chr5:96528568-96528924	GM12878	blood:	n/a	n/a
41	BCL11A	chr5:96430693-96431212	GM12878	blood:	n/a	chr5:96430902-96430911
42	BCL3	chr5:96430753-96431143	GM12878	blood:	n/a	chr5:96430902-96430911
43	BCL3	chr5:96518637-96519903	A549	lung:	n/a	n/a
44	BCLAF1	chr5:96519046-96519886	GM12878	blood:	n/a	n/a
45	BCLAF1	chr5:96430534-96431334	GM12878	blood:	n/a	chr5:96430902-96430911
46	BCLAF1	chr5:96503107-96503654	GM12878	blood:	n/a	n/a
47	BCLAF1	chr5:96430683-96431174	GM12878	blood:	n/a	chr5:96430902-96430911
48	BHLHE40	chr5:96518655-96519736	HepG2	liver:	n/a	n/a
49	BHLHE40	chr5:96518708-96519746	GM12878	blood:	n/a	n/a
50	BHLHE40	chr5:96518681-96519779	K562	blood:	n/a	n/a

(count:1347 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:96497888-96497938	Hepatocyte	liver:	n/a
2	chr5:96432518-96432568	HCF	heart:	n/a
3	chr5:96519465-96519515	HAEpiC	amniotic membrane:	n/a
4	chr5:96522767-96522817	ProgFib	skin:	n/a
5	chr5:96497888-96497938	HepG2	liver:	n/a
6	chr5:96497888-96497938	Hepatocyte	liver:	n/a
7	chr5:96432518-96432568	HCF	heart:	n/a
8	chr5:96519465-96519515	HAEpiC	amniotic membrane:	n/a
9	chr5:96522767-96522817	ProgFib	skin:	n/a
10	chr5:96497888-96497938	HepG2	liver:	n/a
11	chr5:96478514-96478564	GM12891	blood:	n/a
12	chr5:96517289-96517339	MCF10A-Er-Src	breast:	n/a
13	chr5:96479253-96479303	SK-N-SH	brain:	n/a
14	chr5:96477502-96477552	PANC-1	pancreas:	n/a
15	chr5:96479253-96479303	SAEC	small airway:	n/a
16	chr5:96519401-96519451	MCF10A-Er-Src	breast:	n/a
17	chr5:96519566-96519616	HPAEpiC	pulmonary alveolar:	n/a
18	chr5:96519010-96519060	HMEC	breast:	n/a
19	chr5:96452274-96452324	HAEpiC	amniotic membrane:	n/a
20	chr5:96479253-96479303	A549	lung:	n/a
21	chr5:96478495-96478545	AG09319	gingival:	n/a
22	chr5:96519005-96519055	HUVEC	blood vessel:	n/a
23	chr5:96478514-96478564	HUVEC	blood vessel:	n/a
24	chr5:96518721-96518771	HUVEC	blood vessel:	n/a
25	chr5:96519005-96519055	HCM	heart:	n/a
26	chr5:96519005-96519055	GM12878	blood:	n/a
27	chr5:96471792-96471842	BE2_C	brain:	n/a
28	chr5:96471792-96471842	Jurkat	blood:	n/a
29	chr5:96477502-96477552	Hepatocyte	liver:	n/a
30	chr5:96430437-96430487	AG04450	lung:	fetal
31	chr5:96519465-96519515	K562	blood:	n/a
32	chr5:96519548-96519598	A549	lung:	n/a
33	chr5:96497888-96497938	NH-A	brain:	n/a
34	chr5:96478573-96478623	HL-60	blood:	n/a
35	chr5:96471792-96471842	HRCEpiC	kidney:	n/a
36	chr5:96519010-96519060	ECC-1	luminal epithelium:	n/a
37	chr5:96519010-96519060	HepG2	liver:	n/a
38	chr5:96518721-96518771	ovcar-3	ovarian:	n/a
39	chr5:96430437-96430487	HCPEpiC	choroid plexus:	n/a
40	chr5:96519401-96519451	HAEpiC	amniotic membrane:	n/a
41	chr5:96477502-96477552	HUVEC	blood vessel:	n/a
42	chr5:96479253-96479303	SK-N-SH_RA	brain:	n/a
43	chr5:96478573-96478623	HPAEpiC	pulmonary alveolar:	n/a
44	chr5:96519010-96519060	HRE	kidney:	n/a
45	chr5:96471792-96471842	H1-hESC	embryonic stem cell:	embryo
46	chr5:96477502-96477552	HEEpiC	esophagus:	n/a
47	chr5:96519548-96519598	CMK	blood:	n/a
48	chr5:96519005-96519055	MCF10A-Er-Src	breast:	n/a
49	chr5:96471792-96471842	AoSMC	blood vessel:	n/a
50	chr5:96471792-96471842	PFSK-1	brain:	n/a

(count:93 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr5:96440291..96443005-chr5:96446128..96448616,2	K562	blood:
2	chr5:96078120..96080024-chr5:96498248..96500707,2	K562	blood:
3	chr5:96533022..96535910-chr5:96537589..96540065,2	K562	blood:
4	chr5:96484050..96486367-chr5:96488023..96491599,3	K562	blood:
5	chr5:95949882..95950863-chr5:96497777..96498341,2	K562	blood:
6	chr5:96520831..96523398-chr5:96524932..96527174,2	MCF-7	breast:
7	chr5:96513279..96516622-chr5:96517923..96519975,3	MCF-7	breast:
8	chr5:96521057..96523981-chr5:96536109..96539029,2	K562	blood:
9	chr5:96087099..96087726-chr5:96498883..96499456,2	MCF-7	breast:
10	chr5:96431878..96433663-chr5:96441346..96442854,2	K562	blood:
11	chr5:96513470..96515096-chr5:96518937..96520609,2	MCF-7	breast:
12	chr5:96533022..96535910-chr5:96537589..96540065,2	K562	blood:
13	chr5:96447006..96449161-chr5:96454353..96456736,3	K562	blood:
14	chr5:96087427..96088455-chr5:96497429..96498297,3	MCF-7	breast:
15	chr5:96271154..96273754-chr5:96462535..96464231,2	K562	blood:
16	chr5:96505549..96507976-chr5:96519747..96521338,2	MCF-7	breast:
17	chr5:96549287..96551402-chr5:96556377..96559080,2	K562	blood:
18	chr5:96454080..96455959-chr5:96463185..96466174,2	MCF-7	breast:
19	chr5:96454080..96455959-chr5:96463185..96466174,2	MCF-7	breast:
20	chr11:62608625..62609592-chr5:96518540..96519360,2	Hela-S3	cervix:
21	chr1:21112901..21113842-chr5:96518449..96519338,2	Hela-S3	cervix:
22	chr5:96461333..96463342-chr5:96466148..96468249,2	K562	blood:
23	chr5:96508014..96513294-chr5:96513654..96520413,9	K562	blood:
24	chr5:96447147..96449161-chr5:96455236..96457694,2	K562	blood:
25	chr5:96452324..96455301-chr5:96461206..96463835,3	K562	blood:
26	chr5:96449374..96451547-chr5:96453007..96458409,4	K562	blood:
27	chr5:96521334..96524159-chr5:96530024..96533344,3	K562	blood:
28	chr5:96517585..96519769-chr5:96537536..96540052,2	MCF-7	breast:
29	chr5:96087839..96088456-chr5:96497483..96498165,2	MCF-7	breast:
30	chr5:96270867..96272370-chr5:96475978..96478536,2	MCF-7	breast:
31	chr5:96440291..96443005-chr5:96446128..96448616,2	K562	blood:
32	chr5:96518600..96520567-chr5:96529112..96530644,2	MCF-7	breast:
33	chr5:96381723..96383480-chr5:96500362..96502420,2	K562	blood:
34	chr5:96566532..96567370-chr5:96632847..96633430,3	MCF-7	breast:
35	chr5:96087837..96088851-chr5:96497370..96499403,9	K562	blood:
36	chr5:96203527..96205559-chr5:96508441..96510333,2	K562	blood:
37	chr5:96508014..96513294-chr5:96513654..96520413,9	K562	blood:
38	chr5:96517922..96519748-chr5:96562831..96564407,2	MCF-7	breast:
39	chr5:96422481..96423221-chr5:96497763..96498668,2	K562	blood:
40	chr5:96452324..96455301-chr5:96461206..96463835,3	K562	blood:
41	chr5:96534501..96536985-chr5:96538534..96540888,2	MCF-7	breast:
42	chr5:96381504..96384488-chr5:96474189..96476207,2	K562	blood:
43	chr5:96431878..96433663-chr5:96441346..96442854,2	K562	blood:
44	chr5:96517585..96519769-chr5:96537536..96540052,2	MCF-7	breast:
45	chr5:96142588..96144739-chr5:96517628..96519299,2	MCF-7	breast:
46	chr5:96142348..96145031-chr5:96516210..96518138,3	K562	blood:
47	chr5:96566460..96567205-chr5:96869494..96870442,2	MCF-7	breast:
48	chr5:96269896..96271438-chr5:96517931..96519494,2	MCF-7	breast:
49	chr5:96469286..96471593-chr5:96474372..96477073,2	K562	blood:
50	chr5:96549287..96551402-chr5:96556377..96559080,2	K562	blood:

(count:7 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RIOK2-1	chr5:96523794-96523947	ENSG00000248758.1
2	lnc-LIX1-2	chr5:96518830-96518864	NONHSAT102923
3	lnc-LIX1-2	chr5:96514534-96514897	NONHSAT102923
4	lnc-RIOK2-2	chr5:96563572-96563661	XLOC_004934
5	lnc-CTD-2215E18.1.1-1	chr5:96519303-96519373	ENSG00000251513.1
6	lnc-RIOK2-1	chr5:96537546-96537584	ENSG00000248758.1
7	lnc-RIOK2-2	chr5:96559075-96559398	XLOC_004934

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	RIOK2	hsa-miR-101-3p	chr5:96498716-96498737
2	RIOK2	hsa-miR-155-5p	chr5:96498413-96498438

Variant related genes	Relation type
ENSG00000251054	TF binding region
ENSG00000251513	TF binding region
ENSG00000248758	TF binding region
LIX1	TF binding region
RNU1-73P	TF binding region
RIOK2	TF binding region
ENSG00000251054	CpG island
ENSG00000251513	CpG island
ENSG00000248758	CpG island
LIX1	CpG island
RNU1-73P	CpG island
RIOK2	CpG island
ENSG00000251606	chromatin interactions
ENSG00000246763	chromatin interactions
ENSG00000123975	chromatin interactions
ENSG00000248758	chromatin interactions
ENSG00000251054	chromatin interactions
ENSG00000249180	chromatin interactions
ENSG00000113441	chromatin interactions
ENSG00000058729	chromatin interactions
ENSG00000251513	chromatin interactions
ENSG00000153113	chromatin interactions
ENSG00000265112	chromatin interactions
ENSG00000174136	chromatin interactions
ENSG00000206698	chromatin interactions
ENSG00000145721	chromatin interactions
ENSG00000127483	chromatin interactions
ENSG00000133316	chromatin interactions
ENSG00000164307	chromatin interactions
ENSG00000247121	chromatin interactions

Extended variants
information (count: 5736 )
Associated
traits (count: 83 )

Variant overlapped rSNPs/rCNVs (count:5736 , 50 per page) page: 1 2 3 4 5 6 7 ... 115

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs76229328	chr5:96427412-96427413	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs569595492	chr5:96427457-96427458	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs530822874	chr5:96427459-96427460	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs34417930	chr5:96427481-96427482	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs567432361	chr5:96427519-96427520	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs534527877	chr5:96427527-96427528	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs546652011	chr5:96427543-96427544	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs532593937	chr5:96427559-96427560	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs571414659	chr5:96427583-96427584	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs113472630	chr5:96427608-96427609	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs316233	chr5:96427624-96427625	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
12	rs556929486	chr5:96427634-96427635	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs575586203	chr5:96427655-96427656	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs536931832	chr5:96427674-96427675	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs316234	chr5:96427698-96427699	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
16	rs573352454	chr5:96427739-96427740	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs17630580	chr5:96427776-96427777	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs559444483	chr5:96427811-96427812	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs577810717	chr5:96427821-96427822	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs200865154	chr5:96427853-96427854	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs545163420	chr5:96427892-96427893	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs568483085	chr5:96428015-96428016	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs150038487	chr5:96428100-96428101	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs78763426	chr5:96428111-96428112	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs431298	chr5:96428118-96428119	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs186380846	chr5:96428142-96428143	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs192132285	chr5:96428165-96428166	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs534077953	chr5:96428178-96428179	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs554138155	chr5:96428220-96428221	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs376754986	chr5:96428238-96428239	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs549231488	chr5:96428243-96428244	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs530650811	chr5:96428248-96428249	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs552022120	chr5:96428274-96428275	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs571122700	chr5:96428329-96428330	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs182828037	chr5:96428367-96428368	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs187467807	chr5:96428375-96428376	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs546390351	chr5:96428394-96428395	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs571151746	chr5:96428397-96428398	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs144473023	chr5:96428472-96428473	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs76103423	chr5:96428551-96428552	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs569208178	chr5:96428556-96428557	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs536265975	chr5:96428647-96428648	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs117082285	chr5:96428660-96428661	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs573582896	chr5:96428808-96428809	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs534546445	chr5:96428821-96428822	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs559184373	chr5:96428827-96428828	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs191049861	chr5:96428885-96428886	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs545102202	chr5:96428992-96428993	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs563261745	chr5:96429055-96429056	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs182436125	chr5:96429122-96429123	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:83)

Disease	PMID	Source
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Metanephric adenoma	20802469	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Medulloblastoma	21979893	CNVD
Phyllodes tumor	17334353	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Cancer	16751803	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	17603634	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Melanoma	18172304	CNVD
Glioma	20126413	CNVD
Breast cancer	17393978	CNVD
Cancer	21359685	CNVD
Non-small cell lung cancer	21829676	CNVD
adenomatous polyposis	22470819	CNVD
Cancer	22429812	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Liposarcoma	21253554	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Breast cancer	21858162	CNVD
Leukemia	17361228	CNVD
Myelodysplastic syndrome	18508791	CNVD
5q-syndrome	17576883	CNVD
Gastric cancer	17908304	CNVD
Lung cancer	16740712	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Urothelial carcinoma	21177765	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Barrett''s syndrome	19417022	CNVD
Lung cancer	18438408	CNVD
Retinoblastoma	22278416	CNVD
Bipolar disorder	18458673	CNVD
Thyroid cancer	19087340	CNVD
Breast cancer	21785460	CNVD
Merkel cell carcinoma	19020549	CNVD
Squamous cell cancer	20885788	CNVD
Hepatocellular carcinoma	16750200	CNVD
Neurodevelopmental disorder	22521361	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	17133270	CNVD
Acute myeloid leukemia	20729466	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Acute myeloid leukemia	21251322	CNVD
lymphocytic leukemia	21291569	CNVD
Testicular cancer	18059402	CNVD
Colorectal cancer	16272173	CNVD
Prostate cancer	16573809	CNVD
Basal cell lymphoma	17053054	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Mental retardation	19471318	CNVD
Renal cell carcinoma	18194544	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Cancer	20164920	CNVD
Myelodysplastic syndrome	21251322	CNVD
abnormal development	18461090	CNVD
Myelofibrosis	22110671	CNVD
Colorectal cancer	16774939	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Multiple myeloma	17550852	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Bipolar disorder	19114987	CNVD

Chromatin state (count:2366 , 50 per page) page: 1 2 3 4 5 6 7 ... 48

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:96423200-96430200	Weak transcription	Fetal Muscle Leg	muscle
2	chr5:96425200-96437000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr5:96425400-96428200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
4	chr5:96425600-96430200	Weak transcription	Primary B cells from cord blood	blood
5	chr5:96425600-96430600	Weak transcription	Monocytes-CD14+_RO01746	blood
6	chr5:96425800-96430600	Weak transcription	Primary monocytes fromperipheralblood	blood
7	chr5:96426400-96437200	Weak transcription	Primary B cells from peripheral blood	blood
8	chr5:96426600-96427800	Weak transcription	Primary neutrophils fromperipheralblood	blood
9	chr5:96426800-96430200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
10	chr5:96427000-96427400	Active TSS	K562	blood
11	chr5:96427000-96428800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
12	chr5:96427000-96430200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr5:96427400-96428400	Enhancers	K562	blood
14	chr5:96427400-96429200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
15	chr5:96427800-96429000	Enhancers	Primary neutrophils fromperipheralblood	blood
16	chr5:96428200-96432600	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
17	chr5:96428400-96440000	Weak transcription	K562	blood
18	chr5:96428800-96430800	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
19	chr5:96429000-96432000	Weak transcription	Primary neutrophils fromperipheralblood	blood
20	chr5:96429200-96431000	Strong transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
21	chr5:96429200-96431400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
22	chr5:96429400-96431600	Weak transcription	HUES64 Cell Line	embryonic stem cell
23	chr5:96430000-96434600	Enhancers	Breast Myoepithelial Primary Cells	Breast
24	chr5:96430200-96430600	Enhancers	GM12878-XiMat	blood
25	chr5:96430200-96430800	Genic enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
26	chr5:96430200-96431000	Strong transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
27	chr5:96430200-96431200	Strong transcription	Fetal Muscle Leg	muscle
28	chr5:96430200-96432800	Strong transcription	Primary B cells from cord blood	blood
29	chr5:96430400-96430600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
30	chr5:96430400-96430800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
31	chr5:96430400-96430800	Enhancers	Fetal Thymus	thymus
32	chr5:96430400-96431200	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
33	chr5:96430400-96431400	Enhancers	Dnd41	blood
34	chr5:96430600-96431000	Enhancers	Primary monocytes fromperipheralblood	blood
35	chr5:96430600-96431200	Enhancers	Monocytes-CD14+_RO01746	blood
36	chr5:96430600-96432200	Flanking Active TSS	GM12878-XiMat	blood
37	chr5:96430600-96438000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
38	chr5:96430800-96431400	Enhancers	Primary T helper cells PMA-I stimulated	--
39	chr5:96430800-96434600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
40	chr5:96430800-96438200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
41	chr5:96431000-96431200	Enhancers	Duodenum Mucosa	Duodenum
42	chr5:96431000-96431800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
43	chr5:96431000-96432000	Weak transcription	Primary monocytes fromperipheralblood	blood
44	chr5:96431000-96432200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
45	chr5:96431200-96431400	Enhancers	Brain Substantia Nigra	brain
46	chr5:96431200-96432000	Weak transcription	Fetal Muscle Leg	muscle
47	chr5:96431200-96432200	Weak transcription	Monocytes-CD14+_RO01746	blood
48	chr5:96431200-96433600	Enhancers	HUES48 Cell Line	embryonic stem cell
49	chr5:96431400-96432400	Weak transcription	Brain Substantia Nigra	brain
50	chr5:96431400-96433000	Enhancers	iPS-18 Cell Line	embryonic stem cell

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