Variant report

Variant	nsv1012621
Chromosome Location	chr4:9456977-9802366
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2798)
CpG islands
(count:6665)
Chromatin interactive
region (count:40)
LncRNA
region (count:11)
Mature miRNA
region (count: 1)
miRNA target
sites (count:0)

(count:2798 , 50 per page) page: 1 2 3 4 5 6 7 ... 56

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:9764889-9764976	K562	blood:	n/a	n/a
2	ARID3A	chr4:9705188-9705304	HepG2	liver:	n/a	n/a
3	ATF1	chr4:9693437-9693703	K562	blood:	n/a	n/a
4	ATF1	chr4:9758253-9758343	K562	blood:	n/a	n/a
5	ATF2	chr4:9764713-9765001	GM12878	blood:	n/a	n/a
6	BACH1	chr4:9689846-9689882	H1-hESC	embryonic stem cell:	n/a	n/a
7	BACH1	chr4:9605857-9606056	H1-hESC	embryonic stem cell:	n/a	n/a
8	BACH1	chr4:9784048-9784153	H1-hESC	embryonic stem cell:	n/a	n/a
9	BACH1	chr4:9533750-9534097	H1-hESC	embryonic stem cell:	n/a	n/a
10	BATF	chr4:9697635-9697868	GM12878	blood:	n/a	n/a
11	BATF	chr4:9456872-9457051	GM12878	blood:	n/a	n/a
12	BATF	chr4:9496997-9497347	GM12878	blood:	n/a	n/a
13	BATF	chr4:9605704-9606128	GM12878	blood:	n/a	n/a
14	BATF	chr4:9511904-9512243	GM12878	blood:	n/a	n/a
15	BATF	chr4:9709608-9710002	GM12878	blood:	n/a	n/a
16	BATF	chr4:9560693-9560899	GM12878	blood:	n/a	n/a
17	BATF	chr4:9661377-9661663	GM12878	blood:	n/a	n/a
18	BATF	chr4:9606281-9606749	GM12878	blood:	n/a	n/a
19	BATF	chr4:9609924-9610228	GM12878	blood:	n/a	n/a
20	BATF	chr4:9560631-9560870	GM12878	blood:	n/a	n/a
21	BATF	chr4:9511928-9512224	GM12878	blood:	n/a	n/a
22	BATF	chr4:9637521-9637725	GM12878	blood:	n/a	n/a
23	BATF	chr4:9582796-9583040	GM12878	blood:	n/a	n/a
24	BATF	chr4:9609959-9610276	GM12878	blood:	n/a	n/a
25	BATF	chr4:9661312-9661676	GM12878	blood:	n/a	n/a
26	BATF	chr4:9582818-9583030	GM12878	blood:	n/a	n/a
27	BATF	chr4:9709684-9709950	GM12878	blood:	n/a	n/a
28	BATF	chr4:9481131-9481403	GM12878	blood:	n/a	n/a
29	BATF	chr4:9715614-9715953	GM12878	blood:	n/a	n/a
30	BATF	chr4:9779146-9779367	GM12878	blood:	n/a	n/a
31	BATF	chr4:9547853-9548038	GM12878	blood:	n/a	n/a
32	BATF	chr4:9481132-9481453	GM12878	blood:	n/a	n/a
33	BATF	chr4:9606359-9606745	GM12878	blood:	n/a	n/a
34	BCL11A	chr4:9497025-9497432	GM12878	blood:	n/a	chr4:9497121-9497129
35	BCL11A	chr4:9709736-9710003	GM12878	blood:	n/a	n/a
36	BCL11A	chr4:9605779-9606088	GM12878	blood:	n/a	n/a
37	BCL11A	chr4:9693955-9694191	GM12878	blood:	n/a	n/a
38	BCL11A	chr4:9709714-9709970	GM12878	blood:	n/a	n/a
39	BCL11A	chr4:9637557-9637806	GM12878	blood:	n/a	n/a
40	BCL11A	chr4:9547498-9547747	GM12878	blood:	n/a	n/a
41	BCL11A	chr4:9661303-9661712	GM12878	blood:	n/a	n/a
42	BCL11A	chr4:9606478-9606683	GM12878	blood:	n/a	n/a
43	BCL11A	chr4:9609991-9610319	GM12878	blood:	n/a	n/a
44	BCL11A	chr4:9779122-9779297	GM12878	blood:	n/a	n/a
45	BCL11A	chr4:9609970-9610277	GM12878	blood:	n/a	n/a
46	BCL11A	chr4:9605814-9606174	GM12878	blood:	n/a	n/a
47	BCL11A	chr4:9606348-9606693	GM12878	blood:	n/a	n/a
48	BCL3	chr4:9747374-9747670	GM12878	blood:	n/a	n/a
49	BCL3	chr4:9747263-9747923	GM12878	blood:	n/a	n/a
50	BHLHE40	chr4:9693135-9693538	HepG2	liver:	n/a	chr4:9693155-9693171

(count:6665 , 50 per page) page: 1 2 3 4 5 6 7 ... 134

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:9523653-9523703	K562	blood:	n/a
2	chr4:9534366-9534416	U87	brain:	n/a
3	chr4:9508177-9508227	IMR90	lung:	fetal
4	chr4:9495454-9495504	U87	brain:	n/a
5	chr4:9484735-9484785	NHDF-neo	bronchial:	n/a
6	chr4:9661405-9661455	GM19239	blood:	n/a
7	chr4:9762166-9762216	H1-hESC	embryonic stem cell:	embryo
8	chr4:9510286-9510336	HRCEpiC	kidney:	n/a
9	chr4:9783953-9784003	NT2-D1	testis:	n/a
10	chr4:9457537-9457587	Caco-2	colon:	n/a
11	chr4:9514840-9514890	RPTEC	kidney:	n/a
12	chr4:9604432-9604482	HEK293	kidney:	embryo
13	chr4:9500465-9500515	ovcar-3	ovarian:	n/a
14	chr4:9693516-9693566	U87	brain:	n/a
15	chr4:9604340-9604390	SK-N-SH_RA	brain:	n/a
16	chr4:9783192-9783242	ECC-1	luminal epithelium:	n/a
17	chr4:9523653-9523703	K562	blood:	n/a
18	chr4:9534366-9534416	U87	brain:	n/a
19	chr4:9508177-9508227	IMR90	lung:	fetal
20	chr4:9495454-9495504	U87	brain:	n/a
21	chr4:9484735-9484785	NHDF-neo	bronchial:	n/a
22	chr4:9661405-9661455	GM19239	blood:	n/a
23	chr4:9762166-9762216	H1-hESC	embryonic stem cell:	embryo
24	chr4:9510286-9510336	HRCEpiC	kidney:	n/a
25	chr4:9783953-9784003	NT2-D1	testis:	n/a
26	chr4:9457537-9457587	Caco-2	colon:	n/a
27	chr4:9514840-9514890	RPTEC	kidney:	n/a
28	chr4:9604432-9604482	HEK293	kidney:	embryo
29	chr4:9500465-9500515	ovcar-3	ovarian:	n/a
30	chr4:9693516-9693566	U87	brain:	n/a
31	chr4:9604340-9604390	SK-N-SH_RA	brain:	n/a
32	chr4:9783192-9783242	ECC-1	luminal epithelium:	n/a
33	chr4:9787734-9787784	HEEpiC	esophagus:	n/a
34	chr4:9762166-9762216	AG09309	skin:	n/a
35	chr4:9783965-9784015	U87	brain:	n/a
36	chr4:9499367-9499417	PrEC	prostate:	n/a
37	chr4:9503404-9503454	AG09309	skin:	n/a
38	chr4:9782243-9782293	GM12891	blood:	n/a
39	chr4:9505764-9505814	GM12878	blood:	n/a
40	chr4:9783198-9783248	NH-A	brain:	n/a
41	chr4:9693516-9693566	PrEC	prostate:	n/a
42	chr4:9693764-9693814	HUVEC	blood vessel:	n/a
43	chr4:9696916-9696966	HAEpiC	amniotic membrane:	n/a
44	chr4:9604432-9604482	NT2-D1	testis:	n/a
45	chr4:9696916-9696966	HCF	heart:	n/a
46	chr4:9601996-9602046	AG10803	skin:	n/a
47	chr4:9494487-9494537	GM12892	blood:	n/a
48	chr4:9693312-9693362	Caco-2	colon:	n/a
49	chr4:9505698-9505748	GM06990	blood:	n/a
50	chr4:9494907-9494957	HEK293	kidney:	embryo

(count:40 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:9764792..9765537-chr4:9899989..9900954,5	MCF-7	breast:
2	chr2:91816400..91817015-chr4:9766701..9767270,2	MCF-7	breast:
3	chr4:9763456..9766236-chr4:10014004..10016919,3	K562	blood:
4	chr4:9764793..9765717-chr4:10015113..10016017,3	MCF-7	breast:
5	chr4:4147469..4148009-chr4:9497278..9497791,2	MCF-7	breast:
6	chr2:91816088..91820118-chr4:9765029..9767622,10	MCF-7	breast:
7	chr4:9764428..9765300-chr4:10016550..10017565,3	K562	blood:
8	chr2:91815622..91818416-chr4:9765055..9766802,2	K562	blood:
9	chr4:9766485..9767197-chr4:10016698..10017481,2	MCF-7	breast:
10	chr4:9766226..9767390-chr4:9899951..9901032,8	MCF-7	breast:
11	chr4:9764445..9765327-chr4:10020033..10020988,3	K562	blood:
12	chr4:9699934..9701585-chr4:10019007..10021805,2	K562	blood:
13	chr4:9704873..9705750-chr4:10016280..10017221,3	K562	blood:
14	chr4:4147498..4148004-chr4:9497288..9497793,2	MCF-7	breast:
15	chr1:149221736..149225365-chr4:9763717..9766826,4	MCF-7	breast:
16	chr4:9764866..9765415-chr4:9928949..9929492,2	MCF-7	breast:
17	chr4:9764417..9765133-chr4:10016121..10017439,5	MCF-7	breast:
18	chr2:91815162..91820044-chr4:9763391..9768700,25	MCF-7	breast:
19	chr2:91816443..91817305-chr4:9764390..9765414,6	MCF-7	breast:
20	chr2:91818108..91819097-chr4:9766527..9767180,2	K562	blood:
21	chr2:91818675..91820415-chr4:9765033..9768552,3	K562	blood:
22	chr2:91817635..91819182-chr4:9766044..9767255,9	MCF-7	breast:
23	chr4:9705037..9705657-chr4:9778184..9778690,2	K562	blood:
24	chr2:91818363..91818948-chr4:9766445..9767270,6	MCF-7	breast:
25	chr4:9705037..9705657-chr4:9778184..9778690,2	K562	blood:
26	chr4:9765483..9767943-chr4:10007316..10009788,2	MCF-7	breast:
27	chr4:9533415..9534346-chr4:9660887..9661684,2	MCF-7	breast:
28	chr4:9761130..9763005-chr4:9988480..9990175,2	K562	blood:
29	chr4:9764437..9765430-chr4:10020023..10020916,6	MCF-7	breast:
30	chr4:9764370..9765339-chr4:10015197..10016013,4	MCF-7	breast:
31	chr4:9705013..9706114-chr4:10020117..10020881,3	MCF-7	breast:
32	chr4:9766550..9767471-chr4:10020110..10020837,2	MCF-7	breast:
33	chr4:9533415..9534346-chr4:9660887..9661684,2	MCF-7	breast:
34	chr1:149220703..149225113-chr4:9764948..9767069,4	MCF-7	breast:
35	chr4:9704779..9705714-chr4:10015117..10016069,5	MCF-7	breast:
36	chr2:91816303..91817383-chr4:9764391..9765414,6	MCF-7	breast:
37	chr4:9766486..9767204-chr4:10064960..10065893,2	MCF-7	breast:
38	chr4:9770192..9773137-chr4:10024212..10026749,2	K562	blood:
39	chr2:91815178..91817122-chr4:9765055..9766792,2	K562	blood:
40	chr4:9766848..9767385-chr4:9900038..9900893,4	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-DRD5-15	chr4:9680112-9680551	l_2602_chr4:9680111-9682135_thyroid
2	lnc-DEFB131-1	chr4:9470746-9471694	NONHSAT095133
3	lnc-DRD5-16	chr4:9678932-9679558	NONHSAT095141
4	lnc-SLC2A9-1	chr4:9691882-9692319	XLOC_003881
5	lnc-SLC2A9-2	chr4:9693361-9693365	XLOC_003880
6	lnc-SLC2A9-6	chr4:9681968-9682164	l_2603_chr4:9680179-9682164_kidney
7	lnc-SLC2A9-2	chr4:9682416-9682671	XLOC_003880
8	lnc-SLC2A9-6	chr4:9680180-9680546	l_2603_chr4:9680179-9682164_kidney
9	lnc-SLC2A9-1	chr4:9686325-9686330	XLOC_003881
10	lnc-DRD5-15	chr4:9681973-9682135	l_2602_chr4:9680111-9682135_thyroid
11	lnc-RP11-1396O13.13.1-3	chr4:9555234-9555605	NONHSAT095137

miRNA name	Chromosome Location	mirBase accession
hsa-miR-548i	chr4:9557878-9557899	MIMAT0005935_1

No data

Variant related genes	Relation type
OR7E85P	TF binding region
ENSG00000266246	TF binding region
RNA5SP154	TF binding region
ENSG00000249799	TF binding region
DRD5	TF binding region
ENPP7P11	TF binding region
OR7E84P	TF binding region
OR7E86P	TF binding region
MIR548I2	TF binding region
FAM86MP	TF binding region
ENSG00000249443	TF binding region
UNC93B7	TF binding region
ENSG00000249563	TF binding region
OR7E83P	TF binding region
ALG1L3P	TF binding region
ENSG00000265901	TF binding region
ENSG00000242034	TF binding region
OR7E35P	TF binding region
ENSG00000244004	TF binding region
OR7E85P	CpG island
ENSG00000266246	CpG island
RNA5SP154	CpG island
ENSG00000249799	CpG island
DRD5	CpG island
ENPP7P11	CpG island
OR7E84P	CpG island
OR7E86P	CpG island
MIR548I2	CpG island
FAM86MP	CpG island
ENSG00000249443	CpG island
UNC93B7	CpG island
ENSG00000249563	CpG island
OR7E83P	CpG island
ALG1L3P	CpG island
ENSG00000265901	CpG island
ENSG00000242034	CpG island
OR7E35P	CpG island
ENSG00000244004	CpG island
ENSG00000109667	chromatin interactions
ENSG00000250413	chromatin interactions
ENSG00000206737	chromatin interactions
FBXW7	miRNA target sites

Extended variants
information (count: 20563 )
Associated
traits (count: 63 )

Variant overlapped rSNPs/rCNVs (count:20563 , 50 per page) page: 1 2 3 4 5 6 7 ... 412

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs12501535	chr4:9456977-9456978	Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs148084632	chr4:9456987-9456988	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs112448371	chr4:9456993-9456994	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs201217796	chr4:9457016-9457017	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs534489056	chr4:9457029-9457030	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs192902673	chr4:9457032-9457033	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs574406079	chr4:9457038-9457039	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs146148035	chr4:9457039-9457040	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs113703134	chr4:9457056-9457057	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs369746682	chr4:9457057-9457058	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs577765764	chr4:9457076-9457077	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs544818224	chr4:9457088-9457089	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs553918592	chr4:9457113-9457114	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs552348521	chr4:9457129-9457130	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs571808268	chr4:9457151-9457152	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs369281128	chr4:9457164-9457165	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs10005081	chr4:9457173-9457174	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs560817333	chr4:9457198-9457199	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs551836620	chr4:9457538-9457539	Inactive region	CpG island	1 gene(s)	Overlapped CNVs	n/a
20	rs185441645	chr4:9457540-9457541	Inactive region	CpG island	1 gene(s)	Overlapped CNVs	n/a
21	rs144554416	chr4:9457541-9457542	Inactive region	CpG island	1 gene(s)	Overlapped CNVs	n/a
22	rs113720810	chr4:9457545-9457546	Inactive region	CpG island	1 gene(s)	Overlapped CNVs	n/a
23	rs111477150	chr4:9457551-9457552	Inactive region	CpG island	1 gene(s)	Overlapped CNVs	n/a
24	rs554337241	chr4:9457554-9457555	Inactive region	CpG island	1 gene(s)	Overlapped CNVs	n/a
25	rs189057728	chr4:9457681-9457682	Inactive region	CpG island	1 gene(s)	Overlapped CNVs	n/a
26	rs560542514	chr4:9457682-9457683	Inactive region	CpG island	1 gene(s)	Overlapped CNVs	n/a
27	rs192817960	chr4:9457712-9457713	Inactive region	CpG island	1 gene(s)	Overlapped CNVs	n/a
28	rs75906948	chr4:9466884-9466885	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs56284605	chr4:9469079-9469080	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
30	rs374043619	chr4:9469088-9469089	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
31	rs113641007	chr4:9469119-9469120	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
32	rs567260757	chr4:9469121-9469122	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
33	rs377096777	chr4:9469148-9469149	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
34	rs182031336	chr4:9469247-9469248	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
35	rs540275549	chr4:9469255-9469256	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
36	rs372702553	chr4:9469260-9469261	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
37	rs555783922	chr4:9469303-9469304	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
38	rs7682004	chr4:9469336-9469337	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
39	rs574096519	chr4:9469354-9469355	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
40	rs544810321	chr4:9469365-9469366	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
41	rs563109112	chr4:9469376-9469377	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
42	rs186270472	chr4:9469386-9469387	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
43	rs371668016	chr4:9469396-9469397	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
44	rs554855624	chr4:9469413-9469414	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
45	rs113048535	chr4:9469513-9469514	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
46	rs188784714	chr4:9469525-9469526	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
47	rs560639371	chr4:9469534-9469535	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
48	rs575202102	chr4:9469535-9469536	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
49	rs7673463	chr4:9469572-9469573	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	mRNA abundance
50	rs548706706	chr4:9469573-9469574	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:63)

Disease	PMID	Source
Wilms tumour	21544195	CNVD
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
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
Non-syndromic sensorineural hearing loss	17122850	CNVD
Breast cancer	21858162	CNVD
small cell lung cancer	20016488	CNVD
Urothelial carcinoma	21177765	CNVD
Neuroblastoma	20406844	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Schizophrenia	23813976	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Sinonasal adenocarcinoma	21360264	CNVD
Ependymoma	20639864	CNVD
Breast cancer	17142309	CNVD

Chromatin state (count:1563 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:9453600-9457200	Enhancers	Stomach Mucosa	stomach
2	chr4:9455200-9457200	Enhancers	Duodenum Mucosa	Duodenum
3	chr4:9455800-9457200	Enhancers	Rectal Mucosa Donor 31	rectum
4	chr4:9456400-9457200	Enhancers	Gastric	stomach
5	chr4:9476200-9477000	Bivalent Enhancer	Fetal Brain Male	brain
6	chr4:9476600-9477000	Bivalent/Poised TSS	HUES6 Cell Line	embryonic stem cell
7	chr4:9476600-9477000	Bivalent Enhancer	Fetal Muscle Trunk	muscle
8	chr4:9476600-9477000	Bivalent Enhancer	Fetal Muscle Leg	muscle
9	chr4:9477000-9477400	Enhancers	Brain Inferior Temporal Lobe	brain
10	chr4:9481600-9482000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
11	chr4:9481600-9482000	Enhancers	Rectal Mucosa Donor 31	rectum
12	chr4:9481800-9482000	Enhancers	Duodenum Mucosa	Duodenum
13	chr4:9484800-9503800	Weak transcription	Right Atrium	heart
14	chr4:9495800-9496800	Enhancers	Fetal Thymus	thymus
15	chr4:9496200-9496800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
16	chr4:9496200-9496800	Enhancers	Thymus	Thymus
17	chr4:9496200-9497000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
18	chr4:9496400-9496600	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
19	chr4:9496400-9496800	Enhancers	Primary hematopoietic stem cells	blood
20	chr4:9496600-9499000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
21	chr4:9496800-9499600	Weak transcription	Primary hematopoietic stem cells	blood
22	chr4:9499000-9499200	Bivalent Enhancer	ES-I3 Cell Line	embryonic stem cell
23	chr4:9499000-9499200	Flanking Bivalent TSS/Enh	iPS-15b Cell Line	embryonic stem cell
24	chr4:9499000-9499600	Enhancers	Liver	Liver
25	chr4:9499000-9500400	Bivalent/Poised TSS	iPS-20b Cell Line	embryonic stem cell
26	chr4:9499000-9500600	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
27	chr4:9499200-9499400	Bivalent Enhancer	Fetal Thymus	thymus
28	chr4:9499200-9499600	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Male	--
29	chr4:9499200-9499800	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Female	--
30	chr4:9499200-9499800	Bivalent/Poised TSS	Brain Inferior Temporal Lobe	brain
31	chr4:9499200-9500200	Bivalent Enhancer	Primary hematopoietic stem cells short term culture	blood
32	chr4:9499200-9500200	Bivalent Enhancer	Adipose Nuclei	Adipose
33	chr4:9499200-9500400	Bivalent/Poised TSS	HUES48 Cell Line	embryonic stem cell
34	chr4:9499200-9500400	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
35	chr4:9499200-9500600	Active TSS	H9 Cell Line	embryonic stem cell
36	chr4:9499200-9500600	Bivalent/Poised TSS	HUES6 Cell Line	embryonic stem cell
37	chr4:9499200-9500600	Bivalent/Poised TSS	HUES64 Cell Line	embryonic stem cell
38	chr4:9499200-9500600	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
39	chr4:9499200-9500600	Active TSS	Breast Myoepithelial Primary Cells	Breast
40	chr4:9499400-9499600	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
41	chr4:9499400-9499600	Bivalent/Poised TSS	Foreskin Fibroblast Primary Cells skin02	Skin
42	chr4:9499400-9499600	Active TSS	Brain Germinal Matrix	brain
43	chr4:9499400-9499600	Enhancers	Colonic Mucosa	Colon
44	chr4:9499400-9499600	Active TSS	Fetal Brain Female	brain
45	chr4:9499400-9499800	Bivalent/Poised TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
46	chr4:9499400-9499800	Enhancers	Lung	lung
47	chr4:9499400-9500200	Bivalent/Poised TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
48	chr4:9499400-9500400	Bivalent/Poised TSS	iPS-18 Cell Line	embryonic stem cell
49	chr4:9499400-9500400	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
50	chr4:9499400-9500600	Bivalent/Poised TSS	H1 Cell Line	embryonic stem cell

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