Variant report

Variant	nsv883418
Chromosome Location	chr6:5307432-5501389
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2089)
CpG islands
(count:732)
Chromatin interactive
region (count:110)
LncRNA
region (count:7)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2089 , 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	chr6:5471245-5471536	K562	blood:	n/a	n/a
2	ARID3A	chr6:5333915-5334256	HepG2	liver:	n/a	n/a
3	ARID3A	chr6:5351954-5352010	K562	blood:	n/a	n/a
4	ARID3A	chr6:5380018-5380168	K562	blood:	n/a	n/a
5	ARID3A	chr6:5466765-5467343	K562	blood:	n/a	n/a
6	ARID3A	chr6:5329295-5329331	K562	blood:	n/a	n/a
7	ATF1	chr6:5398731-5399051	K562	blood:	n/a	n/a
8	ATF1	chr6:5329106-5329358	K562	blood:	n/a	n/a
9	ATF1	chr6:5400979-5401008	K562	blood:	n/a	n/a
10	ATF2	chr6:5335131-5335747	GM12878	blood:	n/a	n/a
11	ATF2	chr6:5486322-5486870	GM12878	blood:	n/a	n/a
12	ATF2	chr6:5338294-5338813	GM12878	blood:	n/a	n/a
13	ATF2	chr6:5486408-5486752	GM12878	blood:	n/a	n/a
14	BACH1	chr6:5466733-5467034	H1-hESC	embryonic stem cell:	n/a	n/a
15	BACH1	chr6:5472378-5472661	H1-hESC	embryonic stem cell:	n/a	n/a
16	BACH1	chr6:5380041-5380208	K562	blood:	n/a	n/a
17	BACH1	chr6:5309454-5309486	H1-hESC	embryonic stem cell:	n/a	n/a
18	BATF	chr6:5338444-5338732	GM12878	blood:	n/a	n/a
19	BATF	chr6:5486405-5486840	GM12878	blood:	n/a	n/a
20	BATF	chr6:5335214-5335580	GM12878	blood:	n/a	n/a
21	BATF	chr6:5338449-5338757	GM12878	blood:	n/a	n/a
22	BATF	chr6:5486359-5486772	GM12878	blood:	n/a	n/a
23	BATF	chr6:5335227-5335571	GM12878	blood:	n/a	n/a
24	BCL11A	chr6:5486472-5486770	GM12878	blood:	n/a	n/a
25	BCL11A	chr6:5439210-5439426	H1-hESC	embryonic stem cell:	n/a	n/a
26	BCL3	chr6:5486426-5486800	GM12878	blood:	n/a	n/a
27	BCLAF1	chr6:5335203-5335640	GM12878	blood:	n/a	chr6:5335547-5335556
28	BCLAF1	chr6:5486462-5486879	GM12878	blood:	n/a	n/a
29	BCLAF1	chr6:5486464-5486825	GM12878	blood:	n/a	n/a
30	BCLAF1	chr6:5338441-5338757	GM12878	blood:	n/a	chr6:5338528-5338537
31	BHLHE40	chr6:5379969-5380169	GM12878	blood:	n/a	n/a
32	BHLHE40	chr6:5329195-5329272	K562	blood:	n/a	n/a
33	BHLHE40	chr6:5475344-5475513	K562	blood:	n/a	n/a
34	BHLHE40	chr6:5471216-5471558	K562	blood:	n/a	n/a
35	BHLHE40	chr6:5467008-5467253	K562	blood:	n/a	n/a
36	BHLHE40	chr6:5486474-5486846	GM12878	blood:	n/a	n/a
37	BRCA1	chr6:5411934-5412037	Hela-S3	cervix:	n/a	n/a
38	CBX3	chr6:5324140-5324580	K562	blood:	n/a	n/a
39	CBX3	chr6:5324194-5324573	K562	blood:	n/a	n/a
40	CEBPB	chr6:5402661-5402938	K562	blood:	n/a	n/a
41	CEBPB	chr6:5471226-5471535	A549	lung:	n/a	chr6:5471398-5471409
42	CEBPB	chr6:5472487-5472649	H1-hESC	embryonic stem cell:	n/a	n/a
43	CEBPB	chr6:5444631-5444694	K562	blood:	n/a	n/a
44	CEBPB	chr6:5394541-5394893	IMR90	lung:	n/a	chr6:5394716-5394727
45	CEBPB	chr6:5351711-5352308	A549	lung:	n/a	chr6:5352011-5352020 chr6:5352011-5352020 chr6:5352009-5352020 chr6:5352011-5352020 chr6:5352009-5352022 chr6:5352011-5352020
46	CEBPB	chr6:5394513-5394800	K562	blood:	n/a	chr6:5394716-5394727
47	CEBPB	chr6:5351706-5352213	K562	blood:	n/a	chr6:5352011-5352020 chr6:5352011-5352020 chr6:5352009-5352020 chr6:5352011-5352020 chr6:5352009-5352022 chr6:5352011-5352020
48	CEBPB	chr6:5394537-5394883	HepG2	liver:	n/a	chr6:5394716-5394727
49	CEBPB	chr6:5471262-5471542	Hela-S3	cervix:	n/a	chr6:5471398-5471409
50	CEBPB	chr6:5479007-5479143	K562	blood:	n/a	n/a

(count:732 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:5439460-5439510	HCPEpiC	choroid plexus:	n/a
2	chr6:5404958-5405008	AoSMC	blood vessel:	n/a
3	chr6:5439460-5439510	GM12892	blood:	n/a
4	chr6:5442953-5443003	PFSK-1	brain:	n/a
5	chr6:5404958-5405008	Hepatocyte	liver:	n/a
6	chr6:5313645-5313695	BE2_C	brain:	n/a
7	chr6:5313645-5313695	HIPEpiC	eye:	n/a
8	chr6:5425832-5425882	HIPEpiC	eye:	n/a
9	chr6:5412087-5412137	MCF-7	breast:	n/a
10	chr6:5406020-5406070	AG04450	lung:	fetal
11	chr6:5404958-5405008	HRE	kidney:	n/a
12	chr6:5316922-5316972	AG04449	skin:	fetal
13	chr6:5439460-5439510	HIPEpiC	eye:	n/a
14	chr6:5463751-5463801	HPAEpiC	pulmonary alveolar:	n/a
15	chr6:5412087-5412137	BE2_C	brain:	n/a
16	chr6:5431669-5431719	HRE	kidney:	n/a
17	chr6:5313645-5313695	ProgFib	skin:	n/a
18	chr6:5313645-5313695	T-47D	breast:	n/a
19	chr6:5316922-5316972	NHBE	bronchial:	n/a
20	chr6:5463751-5463801	ProgFib	skin:	n/a
21	chr6:5404958-5405008	GM12878	blood:	n/a
22	chr6:5431669-5431719	CMK	blood:	n/a
23	chr6:5412087-5412137	LNCaP	prostate:	n/a
24	chr6:5431669-5431719	Jurkat	blood:	n/a
25	chr6:5316922-5316972	HepG2	liver:	n/a
26	chr6:5412087-5412137	AG09319	gingival:	n/a
27	chr6:5404958-5405008	GM12892	blood:	n/a
28	chr6:5425832-5425882	U87	brain:	n/a
29	chr6:5442953-5443003	HPAEpiC	pulmonary alveolar:	n/a
30	chr6:5463751-5463801	HRPEpiC	eye:	n/a
31	chr6:5378917-5378967	AG04449	skin:	fetal
32	chr6:5412087-5412137	Hela-S3	cervix:	n/a
33	chr6:5378917-5378967	NB4	blood:	n/a
34	chr6:5313645-5313695	H1-hESC	embryonic stem cell:	embryo
35	chr6:5404958-5405008	NHBE	bronchial:	n/a
36	chr6:5316922-5316972	PFSK-1	brain:	n/a
37	chr6:5378917-5378967	A549	lung:	n/a
38	chr6:5313645-5313695	MCF10A-Er-Src	breast:	n/a
39	chr6:5439460-5439510	PANC-1	pancreas:	n/a
40	chr6:5412087-5412137	Jurkat	blood:	n/a
41	chr6:5378917-5378967	ProgFib	skin:	n/a
42	chr6:5412087-5412137	HMEC	breast:	n/a
43	chr6:5463751-5463801	U87	brain:	n/a
44	chr6:5442953-5443003	HL-60	blood:	n/a
45	chr6:5404958-5405008	HEK293	kidney:	embryo
46	chr6:5472095-5472145	PFSK-1	brain:	n/a
47	chr6:5439460-5439510	PrEC	prostate:	n/a
48	chr6:5406020-5406070	NHBE	bronchial:	n/a
49	chr6:5378917-5378967	NT2-D1	testis:	n/a
50	chr6:5412087-5412137	CMK	blood:	n/a

(count:110 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr6:5485806..5488225-chr6:5489962..5492920,2	K562	blood:
2	chr6:5143575..5144138-chr6:5398465..5399339,2	K562	blood:
3	chr6:5323707..5326276-chr6:5329133..5331071,2	K562	blood:
4	chr6:5435025..5437230-chr6:5438877..5440438,2	MCF-7	breast:
5	chr6:5469656..5471454-chr6:5488519..5490118,2	K562	blood:
6	chr6:5354142..5357037-chr6:5358520..5360420,2	K562	blood:
7	chr6:5422309..5423241-chr6:6547390..6547945,3	MCF-7	breast:
8	chr6:5356672..5358762-chr6:5360755..5363627,2	K562	blood:
9	chr6:5422015..5424265-chr6:5433420..5435571,2	K562	blood:
10	chr6:5378846..5381566-chr6:5383901..5386296,2	K562	blood:
11	chr6:5471461..5471990-chr6:5766502..5767102,2	K562	blood:
12	chr6:5214746..5216032-chr6:5379652..5380557,3	K562	blood:
13	chr6:5337400..5339933-chr6:5352570..5354341,2	K562	blood:
14	chr6:5499395..5501300-chr6:5509807..5511478,2	K562	blood:
15	chr6:5056624..5057532-chr6:5398465..5398983,2	K562	blood:
16	chr6:5364063..5367061-chr6:5369428..5371092,2	K562	blood:
17	chr6:5364063..5366771-chr6:5369592..5371297,2	K562	blood:
18	chr6:5470888..5471844-chr6:6131906..6132435,2	MCF-7	breast:
19	chr6:5255894..5257705-chr6:5381224..5383041,2	K562	blood:
20	chr6:5324825..5326784-chr6:5328920..5331743,2	K562	blood:
21	chr6:5478279..5480478-chr6:5483218..5485001,2	K562	blood:
22	chr6:5485806..5488225-chr6:5489962..5492920,2	K562	blood:
23	chr6:5471238..5471818-chr6:5519987..5520960,2	K562	blood:
24	chr6:5263448..5265308-chr6:5346219..5348013,2	K562	blood:
25	chr6:5220721..5222969-chr6:5379273..5381024,2	K562	blood:
26	chr6:5356672..5358762-chr6:5360755..5363627,2	K562	blood:
27	chr6:5316219..5318124-chr6:5321436..5323216,2	K562	blood:
28	chr6:5455034..5457596-chr6:5459159..5460952,3	K562	blood:
29	chr6:5214686..5215658-chr6:5401229..5403280,10	K562	blood:
30	chr6:5351636..5353650-chr6:5354468..5356338,2	K562	blood:
31	chr6:5470498..5472871-chr6:6545581..6547972,2	MCF-7	breast:
32	chr6:5434559..5437034-chr6:5438817..5440512,2	MCF-7	breast:
33	chr6:5333079..5335354-chr6:5335769..5338319,2	K562	blood:
34	chr6:5478279..5480478-chr6:5483218..5485001,2	K562	blood:
35	chr6:5324825..5326784-chr6:5328920..5331743,2	K562	blood:
36	chr6:5431881..5436604-chr6:5436753..5441713,4	K562	blood:
37	chr6:5308485..5310755-chr6:5312679..5315010,2	K562	blood:
38	chr6:5424951..5427870-chr6:5732837..5734922,2	MCF-7	breast:
39	chr6:5422015..5424265-chr6:5433420..5435571,2	K562	blood:
40	chr6:5352377..5354120-chr6:5360443..5362372,2	K562	blood:
41	chr6:5323707..5326276-chr6:5329133..5331071,2	K562	blood:
42	chr6:5333079..5335354-chr6:5335769..5338319,2	K562	blood:
43	chr6:5434559..5437034-chr6:5438817..5440512,2	MCF-7	breast:
44	chr6:5327778..5330476-chr6:5350802..5353723,2	K562	blood:
45	chr6:5383058..5384884-chr6:5386592..5388274,2	K562	blood:
46	chr6:5445214..5446148-chr7:141145714..141146573,2	MCF-7	breast:
47	chr6:5473023..5474708-chr6:5475378..5477106,2	K562	blood:
48	chr6:5438413..5441149-chr6:5444124..5446462,2	K562	blood:
49	chr6:5473023..5474708-chr6:5475378..5477106,2	K562	blood:
50	chr6:5415440..5417820-chr6:5418569..5420285,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-LYRM4-3	chr6:5451916-5452990	ENSG00000269985.1
2	lnc-LYRM4-3	chr6:5458127-5458308	ENSG00000269985.1
3	lnc-LYRM4-3	chr6:5452701-5452990	ENSG00000269985.1
4	lnc-LYRM4-3	chr6:5458127-5458278	NONHSAT107520
5	lnc-LYRM4-3	chr6:5457186-5457261	ENSG00000269985.1
6	lnc-LYRM4-3	chr6:5457093-5457261	NONHSAT107520
7	lnc-LYRM4-3	chr6:5458127-5458266	ENSG00000269985.1

No data

Variant related genes	Relation type
FARS2	TF binding region
ENSG00000269985	TF binding region
FARS2	CpG island
ENSG00000269985	CpG island
ENSG00000214113	chromatin interactions
ENSG00000145982	chromatin interactions

Extended variants
information (count: 7894 )
Associated
traits (count: 102 )

Variant overlapped rSNPs/rCNVs (count:7894 , 50 per page) page: 1 2 3 4 5 6 7 ... 158

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs9392671	chr6:5307432-5307433	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs559615538	chr6:5307466-5307467	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs574821040	chr6:5307507-5307508	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs6926122	chr6:5307508-5307509	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs77183542	chr6:5307531-5307532	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs531359773	chr6:5307626-5307627	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs549567462	chr6:5307706-5307707	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs564984005	chr6:5307708-5307709	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs532340349	chr6:5307723-5307724	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs145194653	chr6:5307724-5307725	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs376552267	chr6:5307726-5307727	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs190731496	chr6:5307744-5307745	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs554113793	chr6:5307750-5307751	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs183435069	chr6:5307751-5307752	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs577512052	chr6:5307753-5307754	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs187136794	chr6:5307754-5307755	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs112548109	chr6:5307755-5307756	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs546548215	chr6:5307763-5307764	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs549580859	chr6:5307790-5307791	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs190052759	chr6:5307814-5307815	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs371051087	chr6:5307830-5307831	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs183058506	chr6:5307917-5307918	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs534868130	chr6:5307922-5307923	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs113397108	chr6:5307980-5307981	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs576125779	chr6:5308028-5308029	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs553184734	chr6:5308034-5308035	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs574709354	chr6:5308099-5308100	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs187394388	chr6:5308167-5308168	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs557639835	chr6:5308168-5308169	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs141393366	chr6:5308254-5308255	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs543449322	chr6:5308274-5308275	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs59798625	chr6:5308303-5308304	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs147016524	chr6:5308351-5308352	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs56667354	chr6:5308363-5308364	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs367939769	chr6:5308371-5308372	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs114213755	chr6:5308395-5308396	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs559560059	chr6:5308419-5308420	Weak transcription ZNF genes & repeats Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs529899911	chr6:5308451-5308452	Weak transcription ZNF genes & repeats Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs13197047	chr6:5308473-5308474	Weak transcription ZNF genes & repeats Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs142155737	chr6:5308504-5308505	Weak transcription ZNF genes & repeats Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs375766076	chr6:5308585-5308586	Weak transcription ZNF genes & repeats Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs530807792	chr6:5308593-5308594	Weak transcription ZNF genes & repeats Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs377714569	chr6:5308622-5308623	Weak transcription ZNF genes & repeats Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs116052455	chr6:5308625-5308626	Weak transcription ZNF genes & repeats Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs146042258	chr6:5308673-5308674	Weak transcription ZNF genes & repeats Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs148219719	chr6:5308718-5308719	Weak transcription ZNF genes & repeats Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs568515953	chr6:5308740-5308741	Weak transcription ZNF genes & repeats Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs536058193	chr6:5308772-5308773	Weak transcription ZNF genes & repeats Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs185469423	chr6:5308777-5308778	Weak transcription ZNF genes & repeats Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs575942469	chr6:5308787-5308788	Weak transcription ZNF genes & repeats Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:102)

Disease	PMID	Source
Developmental delay	19490664	CNVD
Cancer	21183584	CNVD
Multiple Epiphyseal Dysplasia	20877625	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Glaucoma	18694899	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Prostate cancer	16573809	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	17603634	CNVD
Cancer	20164920	CNVD
Colorectal cancer	21297112	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Follicular lymphoma	20505157	CNVD
Glioblastoma multiforme	21080181	CNVD
Ewing''s sarcoma	21437220	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Leukemia	21518781	CNVD
Cancer	21637783	CNVD
Facial dysmorphism	22105932	CNVD
Medulloblastoma	21979893	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Endometrial cancer	22040021	CNVD
Acute myeloid leukemia	16864856	CNVD
Breast cancer	21264507	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	16751803	CNVD
Bladder cancer	19088036	CNVD
Wilms tumour	21544195	CNVD
Uveal melanoma	21693616	CNVD
Biliary cancer	19435499	CNVD
Malaria	21533027	CNVD
Retinoblastoma	19183342	CNVD
Acute myeloid leukemia	20729466	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Prostate cancer	18632612	CNVD
Myelodysplastic syndrome	21251322	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Breast cancer	21858162	CNVD
Lung cancer	18438408	CNVD
Bladder cancer	21909424	CNVD
Multiple myeloma	17550852	CNVD
Ewing''s sarcoma	17952124	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Gastric cancer	16891809	CNVD
Ovarian cancer	21781307	CNVD
Autism	22495311	CNVD
Autism	21448237	CNVD
Cancer	20164919	CNVD
Melanoma	18172304	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Breast cancer	22844521	CNVD
HIV/AIDS	22844521	CNVD
Ovarian cancer	22844521	CNVD
Prostate cancer	22844521	CNVD
Psoriasis	22844521	CNVD
Rheumatoid arthritis	22844521	CNVD
Sclerosis systemic	22844521	CNVD
Systemic lupus erythematosus	22844521	CNVD
Breast cancer	22522925	CNVD
Breast cancer	21552322	CNVD
Immune disease	21076436	CNVD
Autoimmune disease	19135723	CNVD
Systemic lupus erythematosus	17953491	CNVD
Recurrent Infections	22737222	CNVD
Systemic lupus erythematosus	21904924	CNVD
Ependymoma	19289631	CNVD
small cell lung cancer	20016488	CNVD
Gestational infection	22844521	CNVD
Head circumference	22844521	CNVD
Infertility	22844521	CNVD
Recurrent birth weight diabetes	22844521	CNVD
Obesity	22844521	CNVD
Recurrent pregnancy loss	22844521	CNVD
Intellectual disability	21811512	CNVD
Congenital anomalies of the kidney and urinary tract	18694510	CNVD
Nasopharyngeal cancer	22815911	CNVD
dysmorphism	22105932	CNVD
psychomotor delay	22105932	CNVD
Ovarian cancer	19193619	CNVD
Osteosarcoma	16790693	CNVD
Hepatocellular carcinoma	16750200	CNVD
Basal cell lymphoma	21115979	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Breast cancer	21364760	CNVD
Pancreatic cancer	17952125	CNVD
Bipolar disorder	19114987	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:2548 , 50 per page) page: 1 2 3 4 5 6 7 ... 51

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:5280800-5308200	Weak transcription	Primary T cells from cord blood	blood
2	chr6:5287800-5313600	Weak transcription	H9 Cell Line	embryonic stem cell
3	chr6:5288000-5316200	Weak transcription	Fetal Stomach	stomach
4	chr6:5288400-5324000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
5	chr6:5288400-5331000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
6	chr6:5292800-5334400	Weak transcription	Rectal Smooth Muscle	rectum
7	chr6:5295200-5311600	Weak transcription	Small Intestine	intestine
8	chr6:5295400-5325000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
9	chr6:5296200-5316000	Weak transcription	Lung	lung
10	chr6:5301000-5315400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
11	chr6:5301800-5322200	Weak transcription	Ovary	ovary
12	chr6:5302000-5313000	Weak transcription	H1 Cell Line	embryonic stem cell
13	chr6:5302600-5316000	Weak transcription	Brain Inferior Temporal Lobe	brain
14	chr6:5302800-5319200	Weak transcription	Aorta	Aorta
15	chr6:5303000-5308400	Weak transcription	Cortex derived primary cultured neurospheres	brain
16	chr6:5303200-5316000	Weak transcription	Brain Hippocampus Middle	brain
17	chr6:5303200-5368800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
18	chr6:5303600-5310600	Weak transcription	Brain Cingulate Gyrus	brain
19	chr6:5303600-5313000	Weak transcription	K562	blood
20	chr6:5303600-5314400	Weak transcription	Psoas Muscle	Psoas
21	chr6:5303600-5316000	Weak transcription	Brain Anterior Caudate	brain
22	chr6:5303600-5317400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
23	chr6:5303600-5319000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
24	chr6:5303600-5332400	Weak transcription	Gastric	stomach
25	chr6:5303800-5308400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
26	chr6:5303800-5308400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
27	chr6:5303800-5308800	Weak transcription	Esophagus	oesophagus
28	chr6:5303800-5316000	Weak transcription	Stomach Smooth Muscle	stomach
29	chr6:5303800-5316200	Weak transcription	Left Ventricle	heart
30	chr6:5304000-5307800	Weak transcription	NHEK	skin
31	chr6:5304000-5308000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
32	chr6:5304000-5308000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
33	chr6:5304000-5313600	Weak transcription	Primary B cells from peripheral blood	blood
34	chr6:5304000-5320400	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
35	chr6:5304000-5325400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
36	chr6:5304000-5326000	Weak transcription	Primary T cells fromperipheralblood	blood
37	chr6:5304000-5337600	Weak transcription	Primary T helper cells fromperipheralblood	blood
38	chr6:5304200-5308000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
39	chr6:5304200-5308000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
40	chr6:5304200-5308000	Weak transcription	HMEC	breast
41	chr6:5304200-5311000	Weak transcription	Pancreatic Islets	Pancreatic Islet
42	chr6:5304200-5313000	Weak transcription	HUES48 Cell Line	embryonic stem cell
43	chr6:5304200-5314200	Weak transcription	GM12878-XiMat	blood
44	chr6:5304200-5316000	Weak transcription	Fetal Muscle Leg	muscle
45	chr6:5304200-5322800	Weak transcription	Pancreas	Pancrea
46	chr6:5304600-5313000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
47	chr6:5305800-5307800	Enhancers	Fetal Intestine Large	intestine
48	chr6:5306600-5307600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
49	chr6:5306600-5311200	Weak transcription	Skeletal Muscle Female	skeletal muscle
50	chr6:5306800-5308400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung

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