Variant report

Variant	nsv549528
Chromosome Location	chr1:246303128-246708467
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:4995)
CpG islands
(count:3606)
Chromatin interactive
region (count:252)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:4995 , 50 per page) page: 1 2 3 4 5 6 7 ... 100

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:246587912-246588291	K562	blood:	n/a	n/a
2	ARID3A	chr1:246332132-246332717	K562	blood:	n/a	n/a
3	ARID3A	chr1:246345414-246346141	K562	blood:	n/a	n/a
4	ARID3A	chr1:246378134-246379212	K562	blood:	n/a	n/a
5	ARID3A	chr1:246306858-246307142	K562	blood:	n/a	n/a
6	ARID3A	chr1:246495436-246495765	K562	blood:	n/a	n/a
7	ARID3A	chr1:246305649-246306059	K562	blood:	n/a	n/a
8	ARID3A	chr1:246670516-246670577	HepG2	liver:	n/a	n/a
9	ARID3A	chr1:246303129-246303329	HepG2	liver:	n/a	n/a
10	ARID3A	chr1:246303013-246303421	K562	blood:	n/a	n/a
11	ARID3A	chr1:246536567-246536576	K562	blood:	n/a	n/a
12	ARID3A	chr1:246443886-246444158	K562	blood:	n/a	n/a
13	ARID3A	chr1:246383173-246383457	HepG2	liver:	n/a	n/a
14	ARID3A	chr1:246351173-246351659	K562	blood:	n/a	n/a
15	ARID3A	chr1:246364034-246364381	K562	blood:	n/a	n/a
16	ARID3A	chr1:246468839-246469426	K562	blood:	n/a	n/a
17	ARID3A	chr1:246333485-246334689	K562	blood:	n/a	n/a
18	ARID3A	chr1:246340416-246340426	K562	blood:	n/a	n/a
19	ARID3A	chr1:246378433-246378571	HepG2	liver:	n/a	n/a
20	ARID3A	chr1:246472537-246472962	K562	blood:	n/a	n/a
21	ARID3A	chr1:246339570-246339954	K562	blood:	n/a	n/a
22	ARID3A	chr1:246476713-246476913	K562	blood:	n/a	n/a
23	ARID3A	chr1:246329377-246329956	K562	blood:	n/a	n/a
24	ARID3A	chr1:246444896-246445377	HepG2	liver:	n/a	n/a
25	ARID3A	chr1:246469874-246470465	K562	blood:	n/a	n/a
26	ARID3A	chr1:246614048-246614417	K562	blood:	n/a	chr1:246614110-246614126
27	ARID3A	chr1:246660581-246660971	HepG2	liver:	n/a	n/a
28	ARID3A	chr1:246351102-246351709	HepG2	liver:	n/a	n/a
29	ARID3A	chr1:246409804-246409947	K562	blood:	n/a	n/a
30	ARID3A	chr1:246514223-246514241	K562	blood:	n/a	n/a
31	ARID3A	chr1:246591789-246592119	K562	blood:	n/a	n/a
32	ARID3A	chr1:246339492-246340117	HepG2	liver:	n/a	n/a
33	ARID3A	chr1:246315871-246317843	K562	blood:	n/a	n/a
34	ARID3A	chr1:246317239-246317589	HepG2	liver:	n/a	n/a
35	ARID3A	chr1:246660564-246660991	K562	blood:	n/a	n/a
36	ARID3A	chr1:246614088-246614383	HepG2	liver:	n/a	chr1:246614110-246614126
37	ATF1	chr1:246305671-246306307	K562	blood:	n/a	n/a
38	ATF1	chr1:246370614-246370654	K562	blood:	n/a	n/a
39	ATF1	chr1:246345391-246346206	K562	blood:	n/a	n/a
40	ATF1	chr1:246588435-246588914	K562	blood:	n/a	n/a
41	ATF1	chr1:246317155-246317561	K562	blood:	n/a	n/a
42	ATF1	chr1:246507966-246508030	K562	blood:	n/a	n/a
43	ATF1	chr1:246333942-246334272	K562	blood:	n/a	n/a
44	ATF1	chr1:246469981-246470295	K562	blood:	n/a	n/a
45	ATF1	chr1:246445017-246445192	K562	blood:	n/a	n/a
46	ATF1	chr1:246495450-246495686	K562	blood:	n/a	n/a
47	ATF1	chr1:246363474-246363487	K562	blood:	n/a	n/a
48	ATF1	chr1:246501515-246501774	K562	blood:	n/a	n/a
49	ATF1	chr1:246514087-246514345	K562	blood:	n/a	n/a
50	ATF1	chr1:246561390-246561724	K562	blood:	n/a	n/a

(count:3606 , 50 per page) page: 1 2 3 4 5 6 7 ... 73

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:246622633-246622683	HNPCEpiC	eye:	n/a
2	chr1:246518671-246518721	HCT-116	colon:	n/a
3	chr1:246518671-246518721	HEK293	kidney:	embryo
4	chr1:246451744-246451794	NH-A	brain:	n/a
5	chr1:246324811-246324861	MCF10A-Er-Src	breast:	n/a
6	chr1:246518620-246518670	LNCaP	prostate:	n/a
7	chr1:246622483-246622533	BE2_C	brain:	n/a
8	chr1:246622633-246622683	HNPCEpiC	eye:	n/a
9	chr1:246518671-246518721	HCT-116	colon:	n/a
10	chr1:246518671-246518721	HEK293	kidney:	embryo
11	chr1:246451744-246451794	NH-A	brain:	n/a
12	chr1:246324811-246324861	MCF10A-Er-Src	breast:	n/a
13	chr1:246518620-246518670	LNCaP	prostate:	n/a
14	chr1:246622483-246622533	BE2_C	brain:	n/a
15	chr1:246518620-246518670	SK-N-SH	brain:	n/a
16	chr1:246363697-246363747	HCT-116	colon:	n/a
17	chr1:246670940-246670990	AG10803	skin:	n/a
18	chr1:246580717-246580767	SK-N-SH	brain:	n/a
19	chr1:246592123-246592173	T-47D	breast:	n/a
20	chr1:246581705-246581755	HRE	kidney:	n/a
21	chr1:246446300-246446350	MCF10A-Er-Src	breast:	n/a
22	chr1:246672913-246672963	HEK293	kidney:	embryo
23	chr1:246667857-246667907	GM12891	blood:	n/a
24	chr1:246457244-246457294	HIPEpiC	eye:	n/a
25	chr1:246667857-246667907	GM12892	blood:	n/a
26	chr1:246664003-246664053	T-47D	breast:	n/a
27	chr1:246582116-246582166	K562	blood:	n/a
28	chr1:246414665-246414715	HNPCEpiC	eye:	n/a
29	chr1:246581705-246581755	GM12878	blood:	n/a
30	chr1:246415165-246415215	AG04449	skin:	fetal
31	chr1:246670859-246670909	SAEC	small airway:	n/a
32	chr1:246446300-246446350	HNPCEpiC	eye:	n/a
33	chr1:246446300-246446350	AG10803	skin:	n/a
34	chr1:246304208-246304258	H1-hESC	embryonic stem cell:	embryo
35	chr1:246622633-246622683	HEEpiC	esophagus:	n/a
36	chr1:246670217-246670267	SK-N-MC	brain:	n/a
37	chr1:246671665-246671715	HL-60	blood:	n/a
38	chr1:246670726-246670776	AG09319	gingival:	n/a
39	chr1:246580717-246580767	U87	brain:	n/a
40	chr1:246581705-246581755	NHBE	bronchial:	n/a
41	chr1:246415176-246415226	CMK	blood:	n/a
42	chr1:246363574-246363624	HRPEpiC	eye:	n/a
43	chr1:246363574-246363624	AG04450	lung:	fetal
44	chr1:246599230-246599280	CMK	blood:	n/a
45	chr1:246429789-246429839	CMK	blood:	n/a
46	chr1:246670199-246670249	HEK293	kidney:	embryo
47	chr1:246363574-246363624	HNPCEpiC	eye:	n/a
48	chr1:246670726-246670776	GM19239	blood:	n/a
49	chr1:246670726-246670776	HCPEpiC	choroid plexus:	n/a
50	chr1:246415214-246415264	ProgFib	skin:	n/a

(count:252 , 50 per page) page: 1 2 3 4 5 6

No.	Distal block	Cell Line	Cell type
1	chr1:246325662..246328463-chr1:246355771..246358059,2	K562	blood:
2	chr1:246664090..246667600-chr1:246667950..246670801,5	K562	blood:
3	chr1:246407877..246409674-chr1:246412098..246414077,2	K562	blood:
4	chr1:246553361..246555954-chr1:246559201..246561583,2	K562	blood:
5	chr1:246482242..246483844-chr1:246486769..246488361,2	MCF-7	breast:
6	chr1:246361048..246363741-chr1:246366833..246369637,3	K562	blood:
7	chr1:246357127..246361362-chr1:246362304..246364273,3	K562	blood:
8	chr1:246283420..246285442-chr1:246309239..246311230,2	K562	blood:
9	chr1:246331480..246335528-chr1:246374874..246378179,5	K562	blood:
10	chr1:246363848..246365407-chr1:246365927..246368390,2	K562	blood:
11	chr1:246304167..246305874-chr1:246388175..246390883,2	K562	blood:
12	chr1:246175301..246176197-chr1:246366037..246366781,3	MCF-7	breast:
13	chr1:246432947..246435481-chr1:246440603..246442462,2	MCF-7	breast:
14	chr1:246470110..246471825-chr1:246585890..246587442,2	K562	blood:
15	chr1:246660387..246663593-chr1:246664027..246666681,4	MCF-7	breast:
16	chr1:246343018..246344728-chr1:246345131..246347522,2	K562	blood:
17	chr1:246392871..246395828-chr1:246399439..246401491,2	K562	blood:
18	chr1:246576999..246579498-chr1:246580594..246582855,2	K562	blood:
19	chr1:246303201..246305225-chr1:246319673..246321317,2	MCF-7	breast:
20	chr1:246489256..246490981-chr1:246569694..246571729,2	K562	blood:
21	chr1:246297174..246299753-chr1:246320284..246323072,2	K562	blood:
22	chr1:246477291..246479573-chr1:246484385..246486637,2	K562	blood:
23	chr1:246432947..246435481-chr1:246440603..246442462,2	MCF-7	breast:
24	chr1:246521302..246522820-chr1:246527857..246530408,2	K562	blood:
25	chr1:246359779..246363741-chr1:246364321..246369637,8	K562	blood:
26	chr1:246318198..246320733-chr1:246329438..246331827,2	K562	blood:
27	chr1:246548799..246550495-chr1:246559308..246561111,2	K562	blood:
28	chr1:246331853..246336135-chr1:246348494..246351528,4	K562	blood:
29	chr1:246660387..246663593-chr1:246664027..246666681,4	MCF-7	breast:
30	chr1:246463275..246466123-chr1:246471236..246474164,2	MCF-7	breast:
31	chr1:246292574..246294808-chr1:246305134..246306846,2	K562	blood:
32	chr1:246313411..246315648-chr1:246336106..246337851,2	K562	blood:
33	chr1:246660320..246661257-chr1:246916886..246917830,4	K562	blood:
34	chr1:246314921..246318931-chr1:246320889..246326868,8	K562	blood:
35	chr1:246667355..246669348-chr1:246768936..246771912,2	K562	blood:
36	chr1:246458189..246460474-chr1:246462017..246465759,3	K562	blood:
37	chr1:246358405..246360090-chr1:246368790..246371523,2	K562	blood:
38	chr1:246618350..246620200-chr1:246622120..246624573,2	K562	blood:
39	chr1:246463275..246466123-chr1:246471236..246474164,2	MCF-7	breast:
40	chr1:246174027..246176471-chr1:246609850..246611898,2	K562	blood:
41	chr1:246323812..246327417-chr1:246344916..246347036,3	K562	blood:
42	chr1:246704378..246705938-chr1:246830141..246833108,2	K562	blood:
43	chr1:246635326..246636965-chr1:246661670..246663284,2	K562	blood:
44	chr1:246327940..246330525-chr1:246331503..246335844,5	K562	blood:
45	chr1:246643346..246644875-chr1:246651223..246652948,2	K562	blood:
46	chr1:246698102..246699613-chr1:246703690..246706174,2	K562	blood:
47	chr1:246308927..246313479-chr1:246313623..246318049,5	K562	blood:
48	chr1:246345857..246348884-chr1:246378191..246381575,3	K562	blood:
49	chr1:246280440..246281134-chr1:246613800..246614445,2	MCF-7	breast:
50	chr1:246464800..246467604-chr1:246470299..246472286,2	MCF-7	breast:

(count:6 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CNST-2	chr1:246691213-246691457	NONHSAT010708
2	lnc-CNST-2	chr1:246690332-246690503	NONHSAT010708
3	lnc-TFB2M-2	chr1:246485586-246485740	ENSG00000230184.1
4	lnc-TFB2M-2	chr1:246484965-246485170	ENSG00000230184.1
5	lnc-CNST-4	chr1:246342080-246342506	NONHSAT010702
6	lnc-TFB2M-3	chr1:246691864-246692143	NONHSAT010709

No data

Variant related genes	Relation type
ENSG00000227728	TF binding region
CHCHD4P5	TF binding region
ENSG00000229112	TF binding region
SMYD3	TF binding region
ENSG00000242042	TF binding region
SMYD3-IT1	TF binding region
ENSG00000230813	TF binding region
RNU6-1283P	TF binding region
ENSG00000207326	TF binding region
ENSG00000227728	CpG island
CHCHD4P5	CpG island
ENSG00000229112	CpG island
SMYD3	CpG island
ENSG00000242042	CpG island
SMYD3-IT1	CpG island
ENSG00000230813	CpG island
RNU6-1283P	CpG island
ENSG00000207326	CpG island
ENSG00000202184	chromatin interactions
ENSG00000185420	chromatin interactions
ENSG00000225300	chromatin interactions
ENSG00000162852	chromatin interactions
ENSG00000229112	chromatin interactions
ENSG00000166471	chromatin interactions
ENSG00000207326	chromatin interactions
ENSG00000162851	chromatin interactions
ENSG00000230813	chromatin interactions
ENSG00000162714	chromatin interactions
ENSG00000227728	chromatin interactions
ENSG00000230184	chromatin interactions

Extended variants
information (count: 16908 )
Associated
traits (count: 90 )

Variant overlapped rSNPs/rCNVs (count:16908 , 50 per page) page: 1 2 3 4 5 6 7 ... 339

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7551290	chr1:246303128-246303129	Weak transcription Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs548195906	chr1:246303151-246303152	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs567947239	chr1:246303168-246303169	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs184577126	chr1:246303181-246303182	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs543776532	chr1:246303185-246303186	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs547149390	chr1:246303203-246303204	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs79955116	chr1:246303215-246303216	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs7522774	chr1:246303281-246303282	Weak transcription Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs3845511	chr1:246303294-246303295	Weak transcription Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs376352824	chr1:246303327-246303328	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs146774878	chr1:246303350-246303351	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs538135965	chr1:246303381-246303382	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs554966449	chr1:246303400-246303401	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs574716184	chr1:246303417-246303418	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs140718892	chr1:246303423-246303424	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs111279613	chr1:246303433-246303434	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs188551977	chr1:246303456-246303457	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs546064939	chr1:246303530-246303531	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs145916858	chr1:246303541-246303542	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs528706086	chr1:246303549-246303550	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs7515622	chr1:246303561-246303562	Weak transcription Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs181355714	chr1:246303562-246303563	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs527239574	chr1:246303639-246303640	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs186479077	chr1:246303737-246303738	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs543389685	chr1:246303760-246303761	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs148162689	chr1:246303795-246303796	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs189395696	chr1:246303814-246303815	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs10802339	chr1:246303830-246303831	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs141960841	chr1:246303838-246303839	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs554920787	chr1:246303857-246303858	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs150237734	chr1:246303887-246303888	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs572282953	chr1:246303935-246303936	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs138474095	chr1:246303960-246303961	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs547227546	chr1:246303966-246303967	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs56773670	chr1:246303977-246303978	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs546302740	chr1:246304026-246304027	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs562687517	chr1:246304049-246304050	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs142729062	chr1:246304093-246304094	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs147352390	chr1:246304098-246304099	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs561874221	chr1:246304144-246304145	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs139501217	chr1:246304149-246304150	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs540699712	chr1:246304150-246304151	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs564996316	chr1:246304249-246304250	Weak transcription Enhancers Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs563724062	chr1:246304282-246304283	Weak transcription Enhancers Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs532881364	chr1:246304324-246304325	Weak transcription Enhancers Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs79829308	chr1:246304337-246304338	Weak transcription Enhancers Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs569114361	chr1:246304376-246304377	Weak transcription Enhancers Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs181041072	chr1:246304398-246304399	Weak transcription Enhancers Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs548751882	chr1:246304479-246304480	Weak transcription Enhancers Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs201780338	chr1:246304480-246304481	Weak transcription Enhancers Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:90)

Disease	PMID	Source
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Melanoma	18172304	CNVD
Rett syndrome	21593744	CNVD
Medulloblastoma	21979893	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	CNVD
Non-small cell lung cancer	21044232	CNVD
Cervical cancer	21063398	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	20632083	CNVD
Endometrial cancer	22040021	CNVD
Ewing''s sarcoma	21437220	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	21080181	CNVD
Hepatocellular carcinoma	22174799	CNVD
Medulloblastoma	21292688	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	21264507	CNVD
Liposarcoma	21253554	CNVD
Multiple myeloma	21628407	CNVD
Cancer	16751803	CNVD
Prostate cancer	16705090	CNVD
Neuroblastoma	19435921	CNVD
Breast cancer	17850661	CNVD
Breast cancer	16461572	CNVD
Intracranial tumor	16823260	CNVD
Medulloblastoma	18056178	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Colorectal cancer	16272173	CNVD
Neuroblastoma	21899760	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	16608533	CNVD
Ewing''s sarcoma	22429812	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17001317	CNVD
Acute myeloid leukemia	20729466	CNVD
Testicular germ cell tumor	18059402	CNVD
Neuroblastoma	18923191	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Breast cancer	21509527	CNVD
Urothelial carcinoma	21177765	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Hepatocellular carcinoma	18803288	CNVD
Urothelial tumor	18831757	CNVD
Lung cancer	18438408	CNVD
Medulloblastoma	16783165	CNVD
Basal cell lymphoma	17170743	CNVD
Basal cell lymphoma	17053054	CNVD
Congenital abnormalities	21549014	CNVD
Developmental delay	21549014	CNVD
Mental retardation	21549014	CNVD
small cell lung cancer	20016488	CNVD
Cancer	20164920	CNVD
Cancer	17060936	CNVD
abnormal development	18461090	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Non-small cell lung cancer	21829676	CNVD
Multiple myeloma	16616336	CNVD
Ovarian cancer	21720365	CNVD
Glioblastoma multiforme	22291905	CNVD
Myelofibrosis	22110671	CNVD
Disease	21936942	CNVD
laryngomalacia	21936942	CNVD
GLUT3 deficiency syndrome	20509907	CNVD
Developmental delay	21373258	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Developmental delay	19490664	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Cutaneous malignant melanoma	18794153	CNVD
Astrocytoma	17934521	CNVD
Neurocytoma	17123091	CNVD
Central neurocytomas	17123091	CNVD
Breast cancer	20409316	CNVD
Fibroblasts	17951408	CNVD
Lung cancer	17951408	CNVD
Schizophrenia	20967226	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Bipolar disorder	19114987	CNVD
Schizophrenia	19805367	CNVD
Non-syndromic sensorineural hearing loss	19036926	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Ovarian clear cell carcinoma	21343371	CNVD

Chromatin state (count:3444 , 50 per page) page: 1 2 3 4 5 6 7 ... 69

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:246272400-246312000	Weak transcription	Gastric	stomach
2	chr1:246277800-246327800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr1:246281000-246304000	Weak transcription	Primary T cells from cord blood	blood
4	chr1:246281200-246310800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
5	chr1:246281200-246311400	Weak transcription	Primary B cells from cord blood	blood
6	chr1:246281200-246311400	Weak transcription	Primary hematopoietic stem cells	blood
7	chr1:246281800-246306400	Weak transcription	Primary T helper cells fromperipheralblood	blood
8	chr1:246301400-246306600	Enhancers	NHLF	lung
9	chr1:246301600-246306600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
10	chr1:246302000-246306600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
11	chr1:246302000-246306600	Enhancers	HMEC	breast
12	chr1:246302200-246304000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
13	chr1:246302200-246304000	Enhancers	Placenta Amnion	Placenta Amnion
14	chr1:246302200-246304000	Enhancers	HSMM	muscle
15	chr1:246302200-246306000	Enhancers	Muscle Satellite Cultured Cells	--
16	chr1:246302200-246306200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
17	chr1:246302200-246306400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
18	chr1:246302200-246306400	Enhancers	NHEK	skin
19	chr1:246302200-246306600	Enhancers	A549	lung
20	chr1:246302200-246306600	Enhancers	NH-A	brain
21	chr1:246302200-246306600	Enhancers	NHDF-Ad	bronchial
22	chr1:246302200-246306600	Enhancers	Osteobl	bone
23	chr1:246302400-246303200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
24	chr1:246302400-246303400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
25	chr1:246302400-246304800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
26	chr1:246302400-246310200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
27	chr1:246302600-246303200	Weak transcription	Placenta	Placenta
28	chr1:246302600-246303400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
29	chr1:246302600-246303600	Enhancers	HUVEC	blood vessel
30	chr1:246302600-246303800	Enhancers	Hela-S3	cervix
31	chr1:246302600-246306200	Weak transcription	HepG2	liver
32	chr1:246302800-246303200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
33	chr1:246302800-246303600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
34	chr1:246302800-246303600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
35	chr1:246302800-246303800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
36	chr1:246303000-246303600	Genic enhancers	K562	blood
37	chr1:246303000-246311600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
38	chr1:246303200-246304400	Enhancers	Placenta	Placenta
39	chr1:246303200-246306400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
40	chr1:246303400-246304200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
41	chr1:246303400-246305200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
42	chr1:246303600-246304200	Enhancers	K562	blood
43	chr1:246303600-246304800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
44	chr1:246303600-246305400	Weak transcription	HUVEC	blood vessel
45	chr1:246303600-246306000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
46	chr1:246303800-246305800	Weak transcription	Hela-S3	cervix
47	chr1:246303800-246307800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
48	chr1:246304000-246304400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
49	chr1:246304000-246304400	Weak transcription	HSMM	muscle
50	chr1:246304000-246304800	Strong transcription	Primary T cells from cord blood	blood

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