Variant report

Variant	nsv878692
Chromosome Location	chr4:10042160-10099333
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1943)
CpG islands
(count:1221)
Chromatin interactive
region (count:50)
LncRNA
region (count:7)
Mature miRNA
region (count: 1)
miRNA target
sites (count:0)

(count:1943 , 50 per page) page: 1 2 3 4 5 6 7 ... 39

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:10046913-10047474	HepG2	liver:	n/a	n/a
2	ARID3A	chr4:10076206-10076636	HepG2	liver:	n/a	n/a
3	ARID3A	chr4:10048100-10048213	HepG2	liver:	n/a	n/a
4	ATF1	chr4:10097806-10098386	K562	blood:	n/a	n/a
5	ATF2	chr4:10074819-10075282	GM12878	blood:	n/a	n/a
6	ATF2	chr4:10073951-10074707	GM12878	blood:	n/a	n/a
7	ATF2	chr4:10097507-10098531	GM12878	blood:	n/a	n/a
8	ATF2	chr4:10065076-10065700	H1-hESC	embryonic stem cell:	n/a	n/a
9	ATF2	chr4:10097610-10098628	GM12878	blood:	n/a	n/a
10	ATF3	chr4:10065432-10065612	K562	blood:	n/a	n/a
11	ATF3	chr4:10065333-10065626	K562	blood:	n/a	n/a
12	ATF3	chr4:10076299-10076674	K562	blood:	n/a	n/a
13	BACH1	chr4:10097797-10098067	K562	blood:	n/a	n/a
14	BACH1	chr4:10065380-10065672	H1-hESC	embryonic stem cell:	n/a	n/a
15	BCL11A	chr4:10065092-10065386	H1-hESC	embryonic stem cell:	n/a	n/a
16	BCL3	chr4:10074254-10074871	K562	blood:	n/a	n/a
17	BCLAF1	chr4:10075541-10075846	GM12878	blood:	n/a	n/a
18	BCLAF1	chr4:10073951-10074727	GM12878	blood:	n/a	n/a
19	BCLAF1	chr4:10097634-10098303	GM12878	blood:	n/a	n/a
20	BCLAF1	chr4:10073797-10074545	GM12878	blood:	n/a	n/a
21	BHLHE40	chr4:10072883-10073011	K562	blood:	n/a	n/a
22	BHLHE40	chr4:10098006-10098224	GM12878	blood:	n/a	n/a
23	BHLHE40	chr4:10097838-10098171	K562	blood:	n/a	n/a
24	BRCA1	chr4:10065236-10065323	HepG2	liver:	n/a	n/a
25	BRCA1	chr4:10085296-10085313	HepG2	liver:	n/a	n/a
26	CBX3	chr4:10097750-10098072	K562	blood:	n/a	n/a
27	CBX3	chr4:10047117-10047557	HCT-116	colon:	n/a	n/a
28	CBX3	chr4:10044299-10044537	K562	blood:	n/a	n/a
29	CBX3	chr4:10044228-10044589	K562	blood:	n/a	n/a
30	CBX3	chr4:10046976-10047593	HCT-116	colon:	n/a	n/a
31	CCNT2	chr4:10098530-10098848	K562	blood:	n/a	n/a
32	CEBPB	chr4:10055775-10055917	HepG2	liver:	n/a	chr4:10055872-10055883
33	CEBPB	chr4:10046448-10046748	HepG2	liver:	n/a	chr4:10046600-10046611
34	CEBPB	chr4:10067503-10067657	HepG2	liver:	n/a	chr4:10067602-10067613
35	CEBPB	chr4:10091336-10091621	IMR90	lung:	n/a	n/a
36	CEBPB	chr4:10052869-10053177	IMR90	lung:	n/a	chr4:10053009-10053020
37	CEBPB	chr4:10091312-10091618	HepG2	liver:	n/a	n/a
38	CEBPB	chr4:10091307-10091571	K562	blood:	n/a	n/a
39	CEBPB	chr4:10091277-10091625	A549	lung:	n/a	n/a
40	CEBPB	chr4:10047086-10047402	A549	lung:	n/a	n/a
41	CEBPB	chr4:10051143-10051431	K562	blood:	n/a	n/a
42	CEBPB	chr4:10063339-10063704	IMR90	lung:	n/a	chr4:10063514-10063525
43	CEBPB	chr4:10095325-10095705	IMR90	lung:	n/a	n/a
44	CEBPB	chr4:10067501-10067762	HepG2	liver:	n/a	chr4:10067602-10067613
45	CEBPB	chr4:10097786-10098503	IMR90	lung:	n/a	n/a
46	CEBPB	chr4:10076326-10076562	K562	blood:	n/a	n/a
47	CEBPB	chr4:10067535-10067758	A549	lung:	n/a	chr4:10067602-10067613
48	CEBPB	chr4:10097742-10098540	GM12878	blood:	n/a	n/a
49	CEBPB	chr4:10047036-10047675	HCT-116	colon:	n/a	n/a
50	CEBPB	chr4:10067543-10067719	K562	blood:	n/a	chr4:10067602-10067613

(count:1221 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:10084747-10084797	Hepatocyte	liver:	n/a
2	chr4:10084747-10084797	Hepatocyte	liver:	n/a
3	chr4:10089839-10089889	NB4	blood:	n/a
4	chr4:10095183-10095233	U87	brain:	n/a
5	chr4:10084680-10084730	AG09309	skin:	n/a
6	chr4:10042842-10042892	AG04449	skin:	fetal
7	chr4:10095183-10095233	GM06990	blood:	n/a
8	chr4:10079421-10079471	GM12878	blood:	n/a
9	chr4:10079421-10079471	AG04450	lung:	fetal
10	chr4:10086450-10086500	PANC-1	pancreas:	n/a
11	chr4:10079364-10079414	H1-hESC	embryonic stem cell:	embryo
12	chr4:10084747-10084797	HCPEpiC	choroid plexus:	n/a
13	chr4:10086450-10086500	PFSK-1	brain:	n/a
14	chr4:10086483-10086533	HRCEpiC	kidney:	n/a
15	chr4:10089839-10089889	SK-N-SH_RA	brain:	n/a
16	chr4:10065218-10065268	HCM	heart:	n/a
17	chr4:10079364-10079414	NHBE	bronchial:	n/a
18	chr4:10079421-10079471	U87	brain:	n/a
19	chr4:10042449-10042499	T-47D	breast:	n/a
20	chr4:10095183-10095233	HEEpiC	esophagus:	n/a
21	chr4:10076546-10076596	GM19239	blood:	n/a
22	chr4:10086483-10086533	LNCaP	prostate:	n/a
23	chr4:10082415-10082465	AG09319	gingival:	n/a
24	chr4:10079364-10079414	NT2-D1	testis:	n/a
25	chr4:10084747-10084797	H1-hESC	embryonic stem cell:	embryo
26	chr4:10086450-10086500	AG09309	skin:	n/a
27	chr4:10052335-10052385	NB4	blood:	n/a
28	chr4:10042449-10042499	PrEC	prostate:	n/a
29	chr4:10086483-10086533	HPAEpiC	pulmonary alveolar:	n/a
30	chr4:10082415-10082465	AoSMC	blood vessel:	n/a
31	chr4:10079364-10079414	U87	brain:	n/a
32	chr4:10084747-10084797	SK-N-MC	brain:	n/a
33	chr4:10042198-10042248	Caco-2	colon:	n/a
34	chr4:10084680-10084730	PFSK-1	brain:	n/a
35	chr4:10086450-10086500	BJ	skin:	n/a
36	chr4:10042449-10042499	NB4	blood:	n/a
37	chr4:10089839-10089889	MCF10A-Er-Src	breast:	n/a
38	chr4:10095183-10095233	GM19239	blood:	n/a
39	chr4:10077759-10077809	SK-N-SH_RA	brain:	n/a
40	chr4:10077759-10077809	NB4	blood:	n/a
41	chr4:10042449-10042499	HAEpiC	amniotic membrane:	n/a
42	chr4:10089919-10089969	IMR90	lung:	fetal
43	chr4:10086483-10086533	NHBE	bronchial:	n/a
44	chr4:10077759-10077809	ECC-1	luminal epithelium:	n/a
45	chr4:10077759-10077809	HL-60	blood:	n/a
46	chr4:10079364-10079414	SAEC	small airway:	n/a
47	chr4:10082415-10082465	ECC-1	luminal epithelium:	n/a
48	chr4:10082415-10082465	HEK293	kidney:	embryo
49	chr4:10082415-10082465	AG04450	lung:	fetal
50	chr4:10079364-10079414	Hepatocyte	liver:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr4:10065208..10068130-chr4:10069826..10072455,2	MCF-7	breast:
2	chr4:10073732..10076710-chr4:10079365..10080876,2	K562	blood:
3	chr4:10088244..10091996-chr4:10094895..10098032,3	MCF-7	breast:
4	chr4:10068642..10070302-chr4:10116560..10118469,2	K562	blood:
5	chr4:10081093..10083162-chr4:10083280..10086160,2	MCF-7	breast:
6	chr4:10089641..10094747-chr4:10094922..10099608,4	MCF-7	breast:
7	chr4:10099001..10100865-chr4:10100880..10102425,2	MCF-7	breast:
8	chr4:10098588..10100912-chr4:10117777..10119598,3	MCF-7	breast:
9	chr4:10083462..10086704-chr4:10090004..10092862,3	MCF-7	breast:
10	chr4:10097932..10101732-chr4:10116626..10120469,5	MCF-7	breast:
11	chr4:10063533..10065556-chr4:10116961..10119928,2	K562	blood:
12	chr4:10008558..10010473-chr4:10063451..10065782,2	MCF-7	breast:
13	chr4:10043237..10045316-chr4:10079369..10081759,2	K562	blood:
14	chr4:10079005..10081896-chr4:10084564..10086556,3	K562	blood:
15	chr4:10081223..10082723-chr4:10086537..10088286,2	MCF-7	breast:
16	chr4:10073732..10076710-chr4:10079365..10080876,2	K562	blood:
17	chr4:10053096..10055486-chr4:10058375..10060110,2	K562	blood:
18	chr4:10080904..10082503-chr4:10086648..10088570,2	K562	blood:
19	chr4:10080904..10082503-chr4:10086648..10088570,2	K562	blood:
20	chr4:10080344..10083261-chr4:10099505..10101850,2	MCF-7	breast:
21	chr4:10075241..10078261-chr4:10115554..10118749,4	MCF-7	breast:
22	chr4:10089838..10092130-chr4:10112314..10114162,2	MCF-7	breast:
23	chr4:10060964..10064937-chr4:10066932..10071092,4	K562	blood:
24	chr4:10092915..10094624-chr4:10096149..10098338,2	MCF-7	breast:
25	chr4:10060964..10064937-chr4:10066932..10071092,4	K562	blood:
26	chr4:10095456..10100275-chr4:10105163..10110395,7	MCF-7	breast:
27	chr4:10081223..10082723-chr4:10086537..10088286,2	MCF-7	breast:
28	chr4:10081093..10083162-chr4:10083280..10086160,2	MCF-7	breast:
29	chr4:10019482..10021014-chr4:10065089..10066567,17	MCF-7	breast:
30	chr4:10020071..10021146-chr4:10064556..10066056,33	MCF-7	breast:
31	chr4:10061810..10065204-chr4:10068602..10071736,4	MCF-7	breast:
32	chr4:10083462..10086704-chr4:10090004..10092862,3	MCF-7	breast:
33	chr4:10088625..10091657-chr4:10117426..10119862,3	MCF-7	breast:
34	chr4:10043077..10045943-chr4:10118148..10121673,3	K562	blood:
35	chr4:10085861..10088252-chr4:10117616..10120085,2	MCF-7	breast:
36	chr4:10089641..10094747-chr4:10094922..10099608,4	MCF-7	breast:
37	chr4:10091716..10096918-chr4:10117039..10120240,5	MCF-7	breast:
38	chr4:10079908..10083086-chr4:10118111..10120743,3	MCF-7	breast:
39	chr4:9766486..9767204-chr4:10064960..10065893,2	MCF-7	breast:
40	chr4:10083243..10085127-chr4:10085254..10087510,2	K562	blood:
41	chr4:10050227..10052553-chr4:10054498..10056882,2	K562	blood:
42	chr4:10083243..10085127-chr4:10085254..10087510,2	K562	blood:
43	chr4:10065208..10068130-chr4:10069826..10072455,2	MCF-7	breast:
44	chr4:10061810..10065204-chr4:10068602..10071736,4	MCF-7	breast:
45	chr4:10080509..10086191-chr4:10116536..10120345,7	MCF-7	breast:
46	chr3:78594989..78595560-chr4:10084887..10085729,2	MCF-7	breast:
47	chr4:10092915..10094624-chr4:10096149..10098338,2	MCF-7	breast:
48	chr4:10088339..10092907-chr4:10114333..10120002,8	MCF-7	breast:
49	chr4:10053096..10055486-chr4:10058375..10060110,2	K562	blood:
50	chr4:10094579..10097244-chr4:10117506..10119251,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-DRD5-3	chr4:10069734-10071453	XLOC_003449
2	lnc-DRD5-3	chr4:10072875-10073254	XLOC_003449
3	lnc-WDR1-1	chr4:10069715-10071448	ENSG00000249822
4	lnc-WDR1-1	chr4:10069713-10071448	ENSG00000261490.1
5	lnc-WDR1-1	chr4:10072870-10074643	ENSG00000249822
6	lnc-SLC2A9-3	chr4:10075968-10076289	NONHSAT095158
7	lnc-WDR1-1	chr4:10072870-10074643	ENSG00000261490.1

miRNA name	Chromosome Location	mirBase accession
hsa-miR-3138	chr4:10080246-10080269	MIMAT0015006

No data

Variant related genes	Relation type
MIR3138	TF binding region
WDR1	TF binding region
ENSG00000261490	TF binding region
SLC2A9	TF binding region
MIR3138	CpG island
WDR1	CpG island
ENSG00000261490	CpG island
SLC2A9	CpG island
ENSG00000261490	chromatin interactions
ENSG00000109667	chromatin interactions
ENSG00000264931	chromatin interactions
ENSG00000223086	chromatin interactions
ENSG00000071127	chromatin interactions
ZFHX3	miRNA target sites
KIF5B	miRNA target sites

Extended variants
information (count: 2864 )
Associated
traits (count: 57 )

Variant overlapped rSNPs/rCNVs (count:2864 , 50 per page) page: 1 2 3 4 5 6 7 ... 58

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7679916	chr4:10042160-10042161	Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs376079223	chr4:10042194-10042195	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs564794644	chr4:10042200-10042201	Weak transcription Enhancers	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
4	rs532288193	chr4:10042224-10042225	Weak transcription Enhancers	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
5	rs61446121	chr4:10042242-10042243	Weak transcription Enhancers	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
6	rs371248246	chr4:10042248-10042249	Weak transcription Enhancers	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
7	rs534022513	chr4:10042249-10042250	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs549499266	chr4:10042274-10042275	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs112840815	chr4:10042284-10042285	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs116281574	chr4:10042310-10042311	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs192921166	chr4:10042416-10042417	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs372283675	chr4:10042420-10042421	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs556607708	chr4:10042427-10042428	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs74491687	chr4:10042450-10042451	Weak transcription Enhancers	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
15	rs141899952	chr4:10042458-10042459	Weak transcription Enhancers	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
16	rs184585777	chr4:10042476-10042477	Weak transcription Enhancers	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
17	rs572639768	chr4:10042500-10042501	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs542355696	chr4:10042512-10042513	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs541510472	chr4:10042538-10042539	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs115250951	chr4:10042556-10042557	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs7349721	chr4:10042562-10042563	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs189520054	chr4:10042581-10042582	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs532253684	chr4:10042587-10042588	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs547324027	chr4:10042604-10042605	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs559115240	chr4:10042649-10042650	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs372111556	chr4:10042668-10042669	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs61476037	chr4:10042673-10042674	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs75245044	chr4:10042686-10042687	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs180736486	chr4:10042691-10042692	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs531728395	chr4:10042733-10042734	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs559447363	chr4:10042780-10042781	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs368619294	chr4:10042825-10042826	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs571701349	chr4:10042826-10042827	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs13137074	chr4:10042842-10042843	Weak transcription Enhancers	CpG island	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs554552755	chr4:10042843-10042844	Weak transcription Enhancers	CpG island	1 gene(s)	Overlapped CNVs	n/a
36	rs7685958	chr4:10042850-10042851	Weak transcription Enhancers	CpG island	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs13101785	chr4:10042915-10042916	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs16892534	chr4:10042938-10042939	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs536311325	chr4:10042973-10042974	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs79763149	chr4:10042974-10042975	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs576057936	chr4:10042978-10042979	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs184994201	chr4:10042987-10042988	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs138322155	chr4:10043003-10043004	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs13137343	chr4:10043028-10043029	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs540926293	chr4:10043041-10043042	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs559175174	chr4:10043062-10043063	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs78201117	chr4:10043165-10043166	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs116479950	chr4:10043188-10043189	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs563361068	chr4:10043217-10043218	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs531815837	chr4:10043249-10043250	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:57)

Disease	PMID	Source
Colorectal cancer	16272173	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17603634	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Colorectal cancer	19359472	CNVD
Neuroblastoma	17533364	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Cancer	21637783	CNVD
Melanoma	21693616	CNVD
Squamous cell cancer	21044232	CNVD
Colorectal cancer	20709793	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Non-small cell lung cancer	21044232	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	17387387	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Cervical cancer	21062161	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Glioblastoma multiforme	21080181	CNVD
Chordoma	21602918	CNVD
HIV/AIDS	22032296	CNVD
Neuroblastoma	18923191	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Prostate cancer	18632612	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Breast cancer	21785460	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Breast cancer	21509527	CNVD
Lung cancer	18438408	CNVD
Myelofibrosis	22110671	CNVD
Hirschsprung''s Disease	21712996	CNVD
Schizophrenia	22241247	CNVD
Autosomal-dominant microtia	18179897	CNVD
Glioma	17123091	CNVD
Colorectal cancer	20459617	CNVD
Breast cancer	17133270	CNVD
Sezary syndrome	18413736	CNVD
Breast cancer	21858162	CNVD
small cell lung cancer	20016488	CNVD
Neuroblastoma	20406844	CNVD
Schizophrenia	23813976	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Breast cancer	22522925	CNVD
early-passage human iPS cells	21368824	CNVD

Chromatin state (count:1477 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:10035200-10047400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
2	chr4:10035200-10065600	Weak transcription	Primary T helper cells PMA-I stimulated	--
3	chr4:10035400-10049000	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
4	chr4:10035400-10065200	Weak transcription	Right Ventricle	heart
5	chr4:10035600-10046600	Weak transcription	Gastric	stomach
6	chr4:10035800-10044000	Weak transcription	Primary T cells from cord blood	blood
7	chr4:10035800-10068400	Weak transcription	Aorta	Aorta
8	chr4:10036000-10042600	Weak transcription	Psoas Muscle	Psoas
9	chr4:10036200-10048600	Weak transcription	Right Atrium	heart
10	chr4:10036200-10049800	Weak transcription	Lung	lung
11	chr4:10037000-10043800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
12	chr4:10037000-10052400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
13	chr4:10037000-10056000	Weak transcription	Brain Cingulate Gyrus	brain
14	chr4:10039400-10044000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
15	chr4:10041000-10065000	Weak transcription	Stomach Smooth Muscle	stomach
16	chr4:10041400-10043200	Enhancers	Skeletal Muscle Female	skeletal muscle
17	chr4:10041600-10043200	Enhancers	Skeletal Muscle Male	skeletal muscle
18	chr4:10042000-10043200	Enhancers	Fetal Muscle Leg	muscle
19	chr4:10042000-10050000	Weak transcription	Pancreas	Pancrea
20	chr4:10042200-10044200	Weak transcription	Primary T cells fromperipheralblood	blood
21	chr4:10042600-10043200	Enhancers	Psoas Muscle	Psoas
22	chr4:10043200-10044200	Weak transcription	Psoas Muscle	Psoas
23	chr4:10044000-10044600	ZNF genes & repeats	Primary T helper naive cells fromperipheralblood	blood
24	chr4:10044000-10044800	ZNF genes & repeats	Primary T cells from cord blood	blood
25	chr4:10044200-10044600	ZNF genes & repeats	Monocytes-CD14+_RO01746	blood
26	chr4:10044200-10044800	ZNF genes & repeats	Psoas Muscle	Psoas
27	chr4:10044400-10044600	ZNF genes & repeats	Primary T cells fromperipheralblood	blood
28	chr4:10044400-10044800	ZNF genes & repeats	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
29	chr4:10044400-10044800	ZNF genes & repeats	Primary T helper cells fromperipheralblood	blood
30	chr4:10044600-10045200	Weak transcription	Monocytes-CD14+_RO01746	blood
31	chr4:10044600-10049600	Weak transcription	Primary T cells fromperipheralblood	blood
32	chr4:10044600-10064800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
33	chr4:10044800-10047200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
34	chr4:10044800-10048000	Weak transcription	Primary T cells from cord blood	blood
35	chr4:10044800-10056800	Weak transcription	Psoas Muscle	Psoas
36	chr4:10044800-10058800	Weak transcription	Primary T helper cells fromperipheralblood	blood
37	chr4:10045200-10045600	Enhancers	Monocytes-CD14+_RO01746	blood
38	chr4:10045200-10051200	Enhancers	Primary monocytes fromperipheralblood	blood
39	chr4:10045600-10046600	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
40	chr4:10046000-10046600	Enhancers	Primary hematopoietic stem cells short term culture	blood
41	chr4:10046200-10046600	Enhancers	Primary neutrophils fromperipheralblood	blood
42	chr4:10046400-10046800	Enhancers	Primary B cells from peripheral blood	blood
43	chr4:10046400-10047400	Enhancers	HepG2	liver
44	chr4:10046600-10046800	Enhancers	Monocytes-CD14+_RO01746	blood
45	chr4:10046600-10048400	Weak transcription	Primary neutrophils fromperipheralblood	blood
46	chr4:10046800-10047000	Weak transcription	Primary B cells from peripheral blood	blood
47	chr4:10046800-10047400	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
48	chr4:10046800-10048600	Enhancers	HMEC	breast
49	chr4:10046800-10048800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
50	chr4:10046800-10048800	Enhancers	NHEK	skin

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