Variant report

Variant	nsv549271
Chromosome Location	chr1:227411003-227581017
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2653)
CpG islands
(count:1099)
Chromatin interactive
region (count:206)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2653 , 50 per page) page: 1 2 3 4 5 6 7 ... 54

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:227486272-227486537	K562	blood:	n/a	n/a
2	ARID3A	chr1:227458311-227458510	HepG2	liver:	n/a	n/a
3	ARID3A	chr1:227531951-227532315	K562	blood:	n/a	n/a
4	ARID3A	chr1:227544445-227545868	K562	blood:	n/a	n/a
5	ARID3A	chr1:227488495-227488560	K562	blood:	n/a	n/a
6	ARID3A	chr1:227505270-227505548	K562	blood:	n/a	chr1:227505460-227505468
7	ARID3A	chr1:227501798-227501846	K562	blood:	n/a	n/a
8	ARID3A	chr1:227486766-227487801	K562	blood:	n/a	n/a
9	ARID3A	chr1:227558501-227558605	K562	blood:	n/a	n/a
10	ARID3A	chr1:227495580-227495729	K562	blood:	n/a	n/a
11	ARID3A	chr1:227487094-227487329	HepG2	liver:	n/a	n/a
12	ARID3A	chr1:227448086-227448709	K562	blood:	n/a	n/a
13	ARID3A	chr1:227440024-227440227	K562	blood:	n/a	n/a
14	ARID3A	chr1:227477912-227478203	K562	blood:	n/a	n/a
15	ARID3A	chr1:227442315-227443017	K562	blood:	n/a	n/a
16	ARID3A	chr1:227431984-227432281	K562	blood:	n/a	n/a
17	ARID3A	chr1:227439352-227439739	K562	blood:	n/a	n/a
18	ARID3A	chr1:227422651-227423074	HepG2	liver:	n/a	n/a
19	ARID3A	chr1:227444491-227444687	K562	blood:	n/a	n/a
20	ARID3A	chr1:227430754-227432410	HepG2	liver:	n/a	n/a
21	ARID3A	chr1:227506629-227507137	HepG2	liver:	n/a	n/a
22	ARID3A	chr1:227503786-227504345	HepG2	liver:	n/a	n/a
23	ARID3A	chr1:227500985-227501452	K562	blood:	n/a	chr1:227501334-227501350
24	ARID3A	chr1:227523285-227523658	K562	blood:	n/a	n/a
25	ARID3A	chr1:227506004-227506081	HepG2	liver:	n/a	n/a
26	ARID3A	chr1:227505277-227505568	HepG2	liver:	n/a	chr1:227505460-227505468
27	ARID3A	chr1:227427968-227429251	K562	blood:	n/a	n/a
28	ARID3A	chr1:227567093-227567253	K562	blood:	n/a	n/a
29	ARID3A	chr1:227502071-227502929	K562	blood:	n/a	n/a
30	ARID3A	chr1:227422657-227423113	K562	blood:	n/a	n/a
31	ARID3A	chr1:227556858-227558235	K562	blood:	n/a	n/a
32	ARID3A	chr1:227505968-227506203	K562	blood:	n/a	n/a
33	ARID3A	chr1:227503185-227505058	K562	blood:	n/a	n/a
34	ARID3A	chr1:227431450-227431696	K562	blood:	n/a	n/a
35	ATF1	chr1:227487647-227487797	K562	blood:	n/a	n/a
36	ATF1	chr1:227498051-227498328	K562	blood:	n/a	n/a
37	ATF1	chr1:227470502-227470569	K562	blood:	n/a	n/a
38	ATF1	chr1:227500371-227500640	K562	blood:	n/a	n/a
39	ATF1	chr1:227566906-227567233	K562	blood:	n/a	n/a
40	ATF1	chr1:227523126-227523751	K562	blood:	n/a	n/a
41	ATF1	chr1:227413464-227413737	K562	blood:	n/a	n/a
42	ATF1	chr1:227544834-227545648	K562	blood:	n/a	n/a
43	ATF2	chr1:227506792-227507198	H1-hESC	embryonic stem cell:	n/a	n/a
44	ATF3	chr1:227544924-227545499	A549	lung:	n/a	n/a
45	ATF3	chr1:227511607-227511867	K562	blood:	n/a	n/a
46	ATF3	chr1:227544891-227545503	A549	lung:	n/a	n/a
47	ATF3	chr1:227505126-227505503	K562	blood:	n/a	n/a
48	ATF3	chr1:227544772-227545504	K562	blood:	n/a	n/a
49	BACH1	chr1:227530170-227530431	K562	blood:	n/a	n/a
50	BACH1	chr1:227486974-227486983	K562	blood:	n/a	n/a

(count:1099 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:227505845-227505895	Hela-S3	cervix:	n/a
2	chr1:227505845-227505895	Hela-S3	cervix:	n/a
3	chr1:227506868-227506918	AG04449	skin:	fetal
4	chr1:227506021-227506071	HNPCEpiC	eye:	n/a
5	chr1:227506526-227506576	HMEC	breast:	n/a
6	chr1:227506526-227506576	LNCaP	prostate:	n/a
7	chr1:227506021-227506071	NT2-D1	testis:	n/a
8	chr1:227565776-227565826	HNPCEpiC	eye:	n/a
9	chr1:227505916-227505966	Hela-S3	cervix:	n/a
10	chr1:227505447-227505497	ECC-1	luminal epithelium:	n/a
11	chr1:227505854-227505904	SK-N-MC	brain:	n/a
12	chr1:227506868-227506918	HNPCEpiC	eye:	n/a
13	chr1:227506639-227506689	Jurkat	blood:	n/a
14	chr1:227504721-227504771	PrEC	prostate:	n/a
15	chr1:227505916-227505966	HUVEC	blood vessel:	n/a
16	chr1:227506019-227506069	K562	blood:	n/a
17	chr1:227506513-227506563	Hepatocyte	liver:	n/a
18	chr1:227509201-227509251	ovcar-3	ovarian:	n/a
19	chr1:227557617-227557667	HCPEpiC	choroid plexus:	n/a
20	chr1:227505845-227505895	SAEC	small airway:	n/a
21	chr1:227509201-227509251	MCF-7	breast:	n/a
22	chr1:227505447-227505497	AG10803	skin:	n/a
23	chr1:227505598-227505648	Jurkat	blood:	n/a
24	chr1:227565776-227565826	A549	lung:	n/a
25	chr1:227505598-227505648	H1-hESC	embryonic stem cell:	embryo
26	chr1:227544540-227544590	U87	brain:	n/a
27	chr1:227505598-227505648	HMEC	breast:	n/a
28	chr1:227504721-227504771	AG04450	lung:	fetal
29	chr1:227557617-227557667	NB4	blood:	n/a
30	chr1:227505854-227505904	U87	brain:	n/a
31	chr1:227505916-227505966	HMEC	breast:	n/a
32	chr1:227565776-227565826	GM12892	blood:	n/a
33	chr1:227506868-227506918	Hela-S3	cervix:	n/a
34	chr1:227544540-227544590	HRE	kidney:	n/a
35	chr1:227504721-227504771	LNCaP	prostate:	n/a
36	chr1:227505916-227505966	MCF10A-Er-Src	breast:	n/a
37	chr1:227464259-227464309	HUVEC	blood vessel:	n/a
38	chr1:227505910-227505960	AG09309	skin:	n/a
39	chr1:227506019-227506069	NT2-D1	testis:	n/a
40	chr1:227506021-227506071	HEEpiC	esophagus:	n/a
41	chr1:227506526-227506576	PrEC	prostate:	n/a
42	chr1:227506868-227506918	IMR90	lung:	fetal
43	chr1:227506021-227506071	HUVEC	blood vessel:	n/a
44	chr1:227506526-227506576	T-47D	breast:	n/a
45	chr1:227505854-227505904	GM19239	blood:	n/a
46	chr1:227464259-227464309	ovcar-3	ovarian:	n/a
47	chr1:227504721-227504771	IMR90	lung:	fetal
48	chr1:227506526-227506576	HRPEpiC	eye:	n/a
49	chr1:227544540-227544590	A549	lung:	n/a
50	chr1:227505845-227505895	MCF10A-Er-Src	breast:	n/a

(count:206 , 50 per page) page: 1 2 3 4 5

No.	Distal block	Cell Line	Cell type
1	chr1:227422402..227423241-chr1:227624998..227625702,5	MCF-7	breast:
2	chr1:227545277..227548710-chr1:227557152..227561579,4	K562	blood:
3	chr1:227500962..227504758-chr1:227504964..227507747,3	MCF-7	breast:
4	chr1:227503449..227507598-chr1:227555312..227559110,4	K562	blood:
5	chr1:227504519..227508787-chr1:227521188..227524866,7	K562	blood:
6	chr1:227438042..227439910-chr1:227506389..227508258,2	K562	blood:
7	chr1:227490028..227493033-chr1:227499168..227502183,4	K562	blood:
8	chr1:227461159..227463186-chr1:227466378..227468211,2	MCF-7	breast:
9	chr1:227505544..227508414-chr1:227579779..227582450,2	MCF-7	breast:
10	chr1:227505014..227506615-chr1:227519753..227521661,2	MCF-7	breast:
11	chr1:227510624..227512509-chr1:227521394..227523406,2	K562	blood:
12	chr1:227505771..227506271-chr20:57464151..57464682,2	HCT-116	colon:
13	chr1:227461391..227464005-chr1:227469962..227472348,2	K562	blood:
14	chr1:227505963..227507872-chr1:227540665..227542517,2	MCF-7	breast:
15	chr1:227504778..227506670-chr1:227579538..227582289,3	K562	blood:
16	chr1:227505582..227506201-chr3:119217404..119218268,2	Hela-S3	cervix:
17	chr1:227486302..227488328-chr1:227502025..227504666,2	K562	blood:
18	chr1:227530004..227531829-chr1:227543637..227545711,2	K562	blood:
19	chr1:227461391..227464005-chr1:227469962..227472348,2	K562	blood:
20	chr1:227441285..227444497-chr1:227452902..227455834,3	K562	blood:
21	chr1:227484375..227486737-chr1:227489822..227491362,2	K562	blood:
22	chr1:227483357..227485572-chr1:227486057..227488627,3	K562	blood:
23	chr1:227411051..227412753-chr1:227415183..227417286,2	MCF-7	breast:
24	chr1:227461718..227464574-chr1:227466542..227468149,2	K562	blood:
25	chr1:227528855..227531423-chr1:227534318..227537216,2	K562	blood:
26	chr1:227477234..227482232-chr1:227484947..227488828,5	K562	blood:
27	chr1:227561575..227564648-chr1:227564855..227568643,5	K562	blood:
28	chr1:227457997..227462821-chr1:227486670..227490328,4	K562	blood:
29	chr1:227486106..227489054-chr1:227504943..227506984,3	K562	blood:
30	chr1:227485938..227488164-chr1:227505473..227507925,2	MCF-7	breast:
31	chr1:227515846..227518082-chr1:227521897..227524697,2	MCF-7	breast:
32	chr1:227505349..227507259-chr17:61552926..61555906,2	MCF-7	breast:
33	chr1:227365298..227367002-chr1:227505047..227506997,2	K562	blood:
34	chr1:227491263..227493925-chr1:227500068..227502093,2	MCF-7	breast:
35	chr1:227545277..227548710-chr1:227557152..227561579,4	K562	blood:
36	chr1:227441285..227444497-chr1:227452902..227455834,3	K562	blood:
37	chr1:227504495..227506250-chr1:227537255..227539048,2	K562	blood:
38	chr1:227578119..227581046-chr11:66042464..66044320,2	MCF-7	breast:
39	chr1:227480441..227495625-chr1:227496855..227507828,32	K562	blood:
40	chr1:227459873..227461681-chr1:227504938..227506698,2	MCF-7	breast:
41	chr1:227538792..227542003-chr1:227542964..227545271,3	K562	blood:
42	chr1:227573402..227580584-chr1:227581981..227587587,10	K562	blood:
43	chr1:227487011..227489287-chr1:227501111..227503917,2	MCF-7	breast:
44	chr1:227505566..227506340-chr10:95653162..95653749,2	HCT-116	colon:
45	chr1:227447102..227448619-chr1:227452855..227454756,2	K562	blood:
46	chr1:227484375..227486737-chr1:227489822..227491362,2	K562	blood:
47	chr1:227504024..227506366-chr1:227550798..227554388,3	MCF-7	breast:
48	chr1:227453182..227454826-chr1:227468013..227470218,2	MCF-7	breast:
49	chr1:227411051..227412753-chr1:227415183..227417286,2	MCF-7	breast:
50	chr1:227460250..227462821-chr1:227486670..227489514,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZNF678-5	chr1:227469373-227472002	l_204_chr1:227466302-227471954_brain
2	lnc-ADCK3-6	chr1:227421970-227422486	NONHSAT009917
3	lnc-ADCK3-6	chr1:227422753-227423056	NONHSAT009917
4	lnc-ZNF678-5	chr1:227466303-227468235	l_204_chr1:227466302-227471954_brain
5	lnc-JMJD4-6	chr1:227429631-227429932	NONHSAT009918
6	lnc-JMJD4-6	chr1:227425831-227426320	NONHSAT009918

No data

Variant related genes	Relation type
ENSG00000234277	TF binding region
CDC42BPA	TF binding region
ENSG00000228729	TF binding region
ENSG00000236636	TF binding region
ENSG00000234277	CpG island
CDC42BPA	CpG island
ENSG00000228729	CpG island
ENSG00000236636	CpG island
ENSG00000234277	chromatin interactions
ENSG00000120063	chromatin interactions
ENSG00000228625	chromatin interactions
ENSG00000117450	chromatin interactions
ENSG00000176273	chromatin interactions
ENSG00000087460	chromatin interactions
ENSG00000261501	chromatin interactions
ENSG00000242757	chromatin interactions
ENSG00000138686	chromatin interactions
ENSG00000181873	chromatin interactions
ENSG00000236636	chromatin interactions
ENSG00000159640	chromatin interactions
ENSG00000143776	chromatin interactions
ENSG00000203684	chromatin interactions
ENSG00000163050	chromatin interactions
ENSG00000113845	chromatin interactions
ENSG00000228729	chromatin interactions

Extended variants
information (count: 6507 )
Associated
traits (count: 93 )

Variant overlapped rSNPs/rCNVs (count:6507 , 50 per page) page: 1 2 3 4 5 6 7 ... 131

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2203278	chr1:227411003-227411004	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs185722134	chr1:227411016-227411017	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs537271537	chr1:227411017-227411018	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs551547398	chr1:227411040-227411041	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs566865881	chr1:227411074-227411075	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs570846196	chr1:227411086-227411087	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs191669416	chr1:227411141-227411142	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs552998342	chr1:227411151-227411152	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs574744601	chr1:227411172-227411173	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs535802233	chr1:227411181-227411182	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs143178593	chr1:227411205-227411206	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs181193384	chr1:227411207-227411208	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs72755348	chr1:227411229-227411230	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs546054408	chr1:227411303-227411304	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs186488806	chr1:227411325-227411326	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs12565666	chr1:227411328-227411329	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs540533773	chr1:227411333-227411334	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs74659063	chr1:227411361-227411362	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs372845713	chr1:227411362-227411363	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs368660166	chr1:227411387-227411388	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs191002373	chr1:227411392-227411393	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs528900572	chr1:227411398-227411399	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs550525730	chr1:227411434-227411435	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs572090907	chr1:227411435-227411436	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs201229295	chr1:227411446-227411447	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs10799408	chr1:227411477-227411478	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs574399112	chr1:227411483-227411484	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs72755351	chr1:227411497-227411498	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs142802897	chr1:227411509-227411510	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs570709336	chr1:227411531-227411532	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs534842427	chr1:227411547-227411548	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs138349989	chr1:227411577-227411578	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs546898919	chr1:227411600-227411601	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs534133610	chr1:227411637-227411638	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs182493650	chr1:227411656-227411657	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs556141028	chr1:227411690-227411691	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs557306717	chr1:227411749-227411750	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs373047038	chr1:227411770-227411771	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs115808983	chr1:227411771-227411772	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs557397478	chr1:227411805-227411806	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs373085780	chr1:227411810-227411811	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs558235530	chr1:227411860-227411861	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs7540618	chr1:227411863-227411864	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs540392222	chr1:227411867-227411868	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs113833866	chr1:227411937-227411938	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs555398716	chr1:227411992-227411993	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs531744898	chr1:227412001-227412002	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs186811552	chr1:227412024-227412025	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs574380659	chr1:227412078-227412079	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs562497510	chr1:227412081-227412082	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:93)

Disease	PMID	Source
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Autism	22495311	CNVD
Melanoma	18172304	CNVD
Rett syndrome	21593744	CNVD
Medulloblastoma	21979893	CNVD
Cancer	20164919	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
Acute lymphoblastic leukemia	21098271	CNVD
Breast cancer	17603634	CNVD
Neuroblastoma	21899760	CNVD
Breast cancer	21858162	CNVD
Non-small cell lung cancer	21385341	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	16608533	CNVD
Ewing''s sarcoma	22429812	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17001317	CNVD
Acute myeloid leukemia	21251322	CNVD
Multiple myeloma	17550852	CNVD
Prostate cancer	18632612	CNVD
Acute myeloid leukemia	20729466	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Testicular germ cell tumor	18059402	CNVD
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
Neuroblastoma	18923191	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Breast cancer	21509527	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Urothelial carcinoma	21177765	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Chordoma	18071362	CNVD
T-cell lymphomas	19863542	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hepatocellular carcinoma	18803288	CNVD
Urothelial tumor	18831757	CNVD
Lung cancer	18438408	CNVD
Medulloblastoma	16783165	CNVD
Basal cell lymphoma	17170743	CNVD
Mental retardation	19951919	CNVD
Non-syndromic sensorineural hearing loss	17873649	CNVD
Basal cell lymphoma	17053054	CNVD
Autism	14699429	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Fumarase deficiency	21572526	CNVD
Autism	17483303	CNVD
Kartagener syndrome	16639409	CNVD
Congenital abnormalities	21549014	CNVD
Developmental delay	21549014	CNVD
Mental retardation	21549014	CNVD
small cell lung cancer	20016488	CNVD
Glioblastoma multiforme	21138945	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Cancer	20164920	CNVD
Cancer	17060936	CNVD
Myelofibrosis	22110671	CNVD
abnormal development	18461090	CNVD
Breast cancer	21364760	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:2531 , 50 per page) page: 1 2 3 4 5 6 7 ... 51

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:227348200-227412200	Weak transcription	Fetal Muscle Leg	muscle
2	chr1:227370000-227413600	Weak transcription	HUES6 Cell Line	embryonic stem cell
3	chr1:227376600-227412600	Weak transcription	Fetal Lung	lung
4	chr1:227380200-227421800	Weak transcription	Ovary	ovary
5	chr1:227382000-227414000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
6	chr1:227383600-227421800	Weak transcription	Stomach Smooth Muscle	stomach
7	chr1:227386200-227433400	Weak transcription	Fetal Stomach	stomach
8	chr1:227386400-227413800	Weak transcription	Brain Anterior Caudate	brain
9	chr1:227387000-227413600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
10	chr1:227387400-227414000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
11	chr1:227390600-227413600	Weak transcription	Small Intestine	intestine
12	chr1:227396800-227413600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
13	chr1:227398200-227413600	Weak transcription	NHLF	lung
14	chr1:227398800-227411200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
15	chr1:227398800-227413800	Weak transcription	HUES64 Cell Line	embryonic stem cell
16	chr1:227399400-227411200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
17	chr1:227399400-227415400	Weak transcription	Cortex derived primary cultured neurospheres	brain
18	chr1:227399600-227413200	Weak transcription	HSMM	muscle
19	chr1:227400400-227413000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
20	chr1:227400400-227413000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
21	chr1:227400400-227426800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
22	chr1:227400600-227413000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
23	chr1:227400600-227413000	Weak transcription	NHEK	skin
24	chr1:227400800-227412800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
25	chr1:227401600-227413400	Weak transcription	A549	lung
26	chr1:227402400-227430600	Weak transcription	Pancreas	Pancrea
27	chr1:227403800-227412800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
28	chr1:227404000-227413800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
29	chr1:227404400-227412800	Weak transcription	Muscle Satellite Cultured Cells	--
30	chr1:227405600-227421800	Weak transcription	Gastric	stomach
31	chr1:227406400-227417200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
32	chr1:227407200-227411200	Weak transcription	Brain Cingulate Gyrus	brain
33	chr1:227407200-227413400	Weak transcription	NHDF-Ad	bronchial
34	chr1:227407200-227432400	Weak transcription	Right Ventricle	heart
35	chr1:227407800-227411400	Weak transcription	Brain Inferior Temporal Lobe	brain
36	chr1:227407800-227412600	Weak transcription	Pancreatic Islets	Pancreatic Islet
37	chr1:227408000-227413000	Weak transcription	Primary hematopoietic stem cells	blood
38	chr1:227408000-227413600	Weak transcription	Left Ventricle	heart
39	chr1:227408400-227415200	Weak transcription	Fetal Kidney	kidney
40	chr1:227409200-227412800	Weak transcription	Stomach Mucosa	stomach
41	chr1:227410200-227411600	Enhancers	Fetal Intestine Large	intestine
42	chr1:227410600-227411600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
43	chr1:227410600-227411600	Enhancers	Rectal Mucosa Donor 31	rectum
44	chr1:227410600-227411800	Enhancers	Fetal Intestine Small	intestine
45	chr1:227410800-227411200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
46	chr1:227410800-227411200	Enhancers	Brain Substantia Nigra	brain
47	chr1:227410800-227411400	Enhancers	HepG2	liver
48	chr1:227410800-227411600	Enhancers	Brain Angular Gyrus	brain
49	chr1:227410800-227411800	Enhancers	Brain Hippocampus Middle	brain
50	chr1:227410800-227411800	Enhancers	Duodenum Mucosa	Duodenum

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