Variant report

Variant	nsv534953
Chromosome Location	chr1:46969626-47023671
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2485)
CpG islands
(count:2198)
Chromatin interactive
region (count:146)
LncRNA
region (count:10)
Mature miRNA
region (count: 0)
miRNA target
sites (count:1)

(count:2485 , 50 per page) page: 1 2 3 4 5 6 7 ... 50

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:46987788-46988524	K562	blood:	n/a	n/a
2	ARID3A	chr1:46972101-46972482	K562	blood:	n/a	n/a
3	ARID3A	chr1:46971554-46971754	K562	blood:	n/a	n/a
4	ARID3A	chr1:46982952-46983183	K562	blood:	n/a	n/a
5	ARID3A	chr1:46993569-46993932	K562	blood:	n/a	n/a
6	ATF1	chr1:46972163-46972502	K562	blood:	n/a	n/a
7	ATF1	chr1:46987878-46988860	K562	blood:	n/a	n/a
8	ATF1	chr1:46993520-46994021	K562	blood:	n/a	n/a
9	ATF1	chr1:47002262-47002458	K562	blood:	n/a	n/a
10	ATF1	chr1:47010421-47010912	K562	blood:	n/a	n/a
11	ATF3	chr1:46974451-46974702	K562	blood:	n/a	n/a
12	ATF3	chr1:46974460-46974788	K562	blood:	n/a	n/a
13	ATF3	chr1:47010592-47010880	K562	blood:	n/a	chr1:47010767-47010777
14	ATF3	chr1:46987796-46988568	K562	blood:	n/a	n/a
15	BACH1	chr1:46974512-46974750	H1-hESC	embryonic stem cell:	n/a	chr1:46974605-46974619
16	BACH1	chr1:46998548-46999206	H1-hESC	embryonic stem cell:	n/a	n/a
17	BACH1	chr1:46993894-46993937	H1-hESC	embryonic stem cell:	n/a	n/a
18	BACH1	chr1:46987833-46988484	K562	blood:	n/a	n/a
19	BACH1	chr1:46974498-46974756	K562	blood:	n/a	chr1:46974605-46974619
20	BHLHE40	chr1:47000791-47001167	K562	blood:	n/a	n/a
21	BHLHE40	chr1:47010390-47011163	K562	blood:	n/a	n/a
22	BHLHE40	chr1:46993094-46993096	K562	blood:	n/a	n/a
23	BHLHE40	chr1:47004234-47004311	K562	blood:	n/a	n/a
24	BHLHE40	chr1:46996624-46996672	K562	blood:	n/a	n/a
25	BHLHE40	chr1:47013382-47014007	K562	blood:	n/a	n/a
26	BHLHE40	chr1:47022464-47022843	K562	blood:	n/a	n/a
27	BHLHE40	chr1:46987738-46988761	K562	blood:	n/a	n/a
28	BHLHE40	chr1:46985759-46986670	K562	blood:	n/a	n/a
29	BHLHE40	chr1:46974578-46974689	K562	blood:	n/a	n/a
30	BHLHE40	chr1:46993723-46993978	GM12878	blood:	n/a	n/a
31	BHLHE40	chr1:46992642-46992851	K562	blood:	n/a	n/a
32	BHLHE40	chr1:46993479-46994050	K562	blood:	n/a	n/a
33	BHLHE40	chr1:46999116-46999160	GM12878	blood:	n/a	n/a
34	BHLHE40	chr1:46982920-46982961	K562	blood:	n/a	n/a
35	BHLHE40	chr1:46972228-46972471	K562	blood:	n/a	n/a
36	BHLHE40	chr1:46972740-46972748	K562	blood:	n/a	n/a
37	BRCA1	chr1:46982357-46983241	Hela-S3	cervix:	n/a	n/a
38	BRCA1	chr1:46987719-46988503	Hela-S3	cervix:	n/a	chr1:46988129-46988136
39	BRCA1	chr1:46993702-46994024	Hela-S3	cervix:	n/a	n/a
40	BRCA1	chr1:47013743-47014000	Hela-S3	cervix:	n/a	n/a
41	BRCA1	chr1:46993744-46993913	GM12878	blood:	n/a	n/a
42	BRCA1	chr1:46993803-46994022	H1-hESC	embryonic stem cell:	n/a	n/a
43	CBX3	chr1:46985623-46986360	K562	blood:	n/a	n/a
44	CBX3	chr1:47010306-47011153	K562	blood:	n/a	n/a
45	CBX3	chr1:46974407-46974812	K562	blood:	n/a	n/a
46	CBX3	chr1:46987632-46988897	K562	blood:	n/a	n/a
47	CBX3	chr1:46984677-46985260	K562	blood:	n/a	n/a
48	CBX3	chr1:46972035-46972533	K562	blood:	n/a	n/a
49	CBX3	chr1:46993073-46994045	K562	blood:	n/a	n/a
50	CBX3	chr1:46987800-46988569	K562	blood:	n/a	n/a

(count:2198 , 50 per page) page: 1 2 3 4 5 6 7 ... 44

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:47010131-47010181	Caco-2	colon:	n/a
2	chr1:46999211-46999261	PrEC	prostate:	n/a
3	chr1:47010131-47010181	Caco-2	colon:	n/a
4	chr1:46999211-46999261	PrEC	prostate:	n/a
5	chr1:47009527-47009577	GM12878	blood:	n/a
6	chr1:47017388-47017438	HMEC	breast:	n/a
7	chr1:46989301-46989351	HCF	heart:	n/a
8	chr1:46972470-46972520	T-47D	breast:	n/a
9	chr1:47018319-47018369	GM12891	blood:	n/a
10	chr1:46993347-46993397	Jurkat	blood:	n/a
11	chr1:46999248-46999298	SK-N-SH_RA	brain:	n/a
12	chr1:47023134-47023184	AG09309	skin:	n/a
13	chr1:47010223-47010273	NHDF-neo	bronchial:	n/a
14	chr1:46999211-46999261	AG10803	skin:	n/a
15	chr1:47009809-47009859	Hela-S3	cervix:	n/a
16	chr1:47018072-47018122	HPAEpiC	pulmonary alveolar:	n/a
17	chr1:46999248-46999298	GM12891	blood:	n/a
18	chr1:47003244-47003294	BE2_C	brain:	n/a
19	chr1:47016917-47016967	ECC-1	luminal epithelium:	n/a
20	chr1:46972736-46972786	MCF-7	breast:	n/a
21	chr1:47010105-47010155	SK-N-MC	brain:	n/a
22	chr1:46982889-46982939	HRE	kidney:	n/a
23	chr1:46999348-46999398	BJ	skin:	n/a
24	chr1:47016749-47016799	HL-60	blood:	n/a
25	chr1:46998715-46998765	LNCaP	prostate:	n/a
26	chr1:47015494-47015544	H1-hESC	embryonic stem cell:	embryo
27	chr1:47013178-47013228	NHBE	bronchial:	n/a
28	chr1:46972470-46972520	AG04450	lung:	fetal
29	chr1:47010105-47010155	HCF	heart:	n/a
30	chr1:47005728-47005778	PFSK-1	brain:	n/a
31	chr1:46998715-46998765	HUVEC	blood vessel:	n/a
32	chr1:47023134-47023184	AG10803	skin:	n/a
33	chr1:47015494-47015544	HCPEpiC	choroid plexus:	n/a
34	chr1:46998792-46998842	GM06990	blood:	n/a
35	chr1:47018177-47018227	AG09309	skin:	n/a
36	chr1:47016749-47016799	AG09309	skin:	n/a
37	chr1:47016917-47016967	AG04449	skin:	fetal
38	chr1:46997184-46997234	U87	brain:	n/a
39	chr1:47018072-47018122	A549	lung:	n/a
40	chr1:47005728-47005778	SK-N-MC	brain:	n/a
41	chr1:46999248-46999298	AG09309	skin:	n/a
42	chr1:46999211-46999261	ovcar-3	ovarian:	n/a
43	chr1:47016749-47016799	RPTEC	kidney:	n/a
44	chr1:46999211-46999261	NB4	blood:	n/a
45	chr1:47023134-47023184	Hela-S3	cervix:	n/a
46	chr1:46999348-46999398	BE2_C	brain:	n/a
47	chr1:47016114-47016164	K562	blood:	n/a
48	chr1:47018072-47018122	HNPCEpiC	eye:	n/a
49	chr1:47009527-47009577	HRE	kidney:	n/a
50	chr1:46997184-46997234	LNCaP	prostate:	n/a

(count:146 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr1:46908197..46910490-chr1:46990739..46993641,3	K562	blood:
2	chr1:46912494..46913218-chr1:47000111..47001290,4	MCF-7	breast:
3	chr1:46948519..46951026-chr1:47010382..47012141,2	K562	blood:
4	chr1:46908155..46911848-chr1:46987375..46989663,3	K562	blood:
5	chr1:46995449..46997636-chr1:47000610..47003037,2	K562	blood:
6	chr1:46981951..46984222-chr1:46986722..46989512,3	MCF-7	breast:
7	chr1:46991343..46993867-chr1:46999372..47001574,2	K562	blood:
8	chr1:46937960..46939481-chr1:46992013..46994117,2	K562	blood:
9	chr1:46954136..46954641-chr1:46993665..46994197,2	MCF-7	breast:
10	chr1:46995357..46997930-chr1:46998172..47001101,2	K562	blood:
11	chr1:46913820..46916720-chr1:47006698..47008452,2	K562	blood:
12	chr1:46902494..46904557-chr1:47010678..47013224,2	K562	blood:
13	chr1:46950640..46959255-chr1:46986389..46991936,15	K562	blood:
14	chr1:46907829..46908706-chr1:46998510..46999437,3	K562	blood:
15	chr1:46991986..46993647-chr1:47009898..47012752,2	K562	blood:
16	chr1:46946374..46948781-chr1:47004652..47006176,2	MCF-7	breast:
17	chr1:46981951..46984222-chr1:46986722..46989512,3	MCF-7	breast:
18	chr1:47013364..47014237-chr1:47190848..47191491,2	MCF-7	breast:
19	chr1:47015863..47022104-chr1:47022936..47029939,8	K562	blood:
20	chr1:46942785..46943861-chr1:46992873..46994875,44	K562	blood:
21	chr1:47012476..47015680-chr1:47016269..47019098,3	K562	blood:
22	chr1:46974014..46977516-chr1:46977707..46980613,4	K562	blood:
23	chr1:46957824..46960090-chr1:46991984..46994701,2	K562	blood:
24	chr1:46943865..46944889-chr1:46993729..46994414,5	K562	blood:
25	chr1:46872033..46872647-chr1:47000499..47001417,2	K562	blood:
26	chr1:47000463..47001603-chr1:47013528..47014314,3	K562	blood:
27	chr1:46956868..46959415-chr1:46973779..46975325,2	K562	blood:
28	chr1:46999703..47001765-chr1:47004931..47007448,2	K562	blood:
29	chr1:46974244..46975223-chr1:46982794..46983742,2	K562	blood:
30	chr1:46947988..46950035-chr1:46973534..46976017,2	K562	blood:
31	chr1:47008125..47011332-chr1:47013107..47016538,3	K562	blood:
32	chr1:46979573..46981984-chr1:46991626..46994560,2	K562	blood:
33	chr1:46991986..46993647-chr1:47009898..47012752,2	K562	blood:
34	chr1:46872939..46873670-chr1:47013367..47013915,2	K562	blood:
35	chr1:46956753..46958368-chr1:46973825..46976244,2	K562	blood:
36	chr1:46911278..46913612-chr1:46993367..46994439,12	MCF-7	breast:
37	chr1:46943210..46943796-chr1:46988470..46989208,2	K562	blood:
38	chr1:46993019..46995124-chr1:46997207..47000193,2	K562	blood:
39	chr1:46942850..46943359-chr1:47013489..47014125,2	MCF-7	breast:
40	chr1:47006434..47008326-chr1:47012216..47013817,2	K562	blood:
41	chr1:46920354..46923380-chr1:47007793..47010498,3	K562	blood:
42	chr1:46992642..46995559-chr1:47183422..47185520,2	MCF-7	breast:
43	chr1:46960989..46962798-chr1:46967712..46970240,2	K562	blood:
44	chr1:46870622..46873242-chr1:47000885..47003124,2	K562	blood:
45	chr1:46996193..46996882-chr1:47013438..47014244,2	MCF-7	breast:
46	chr1:46977403..46980726-chr1:46981041..46983666,4	K562	blood:
47	chr1:46913874..46916850-chr1:46987729..46989869,4	K562	blood:
48	chr1:47023201..47026031-chr1:47173277..47176114,2	K562	blood:
49	chr1:46995449..46997636-chr1:47000610..47003037,2	K562	blood:
50	chr1:46953215..46954128-chr1:46993388..46994317,4	MCF-7	breast:

(count:10 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-DMBX1-3	chr1:47003237-47003360	NONHSAT003017
2	lnc-DMBX1-3	chr1:46996534-46996634	NONHSAT003017
3	lnc-DMBX1-2	chr1:47004368-47004466	ENSG00000235894
4	lnc-DMBX1-2	chr1:47006602-47006681	ENSG00000269956.1
5	lnc-DMBX1-2	chr1:47009366-47009440	ENSG00000269956.1
6	lnc-DMBX1-2	chr1:47004368-47004466	ENSG00000269956.1
7	lnc-DMBX1-2	chr1:47006602-47006681	ENSG00000235894
8	lnc-DMBX1-3	chr1:47003944-47004102	NONHSAT003017
9	lnc-DMBX1-2	chr1:47009366-47009440	ENSG00000235894
10	lnc-DMBX1-3	chr1:47005784-47005887	NONHSAT003017

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	KNCN	hsa-miR-1	chr1:47012638-47012659

Variant related genes	Relation type
MKNK1-AS1	TF binding region
KNCN	TF binding region
DMBX1	TF binding region
MKNK1-AS1	CpG island
KNCN	CpG island
DMBX1	CpG island
ENSG00000224863	chromatin interactions
ENSG00000117480	chromatin interactions
ENSG00000225667	chromatin interactions
ENSG00000162456	chromatin interactions
ENSG00000269956	chromatin interactions
ENSG00000079277	chromatin interactions
ENSG00000197587	chromatin interactions
ENSG00000159658	chromatin interactions
CYP1B1	miRNA target sites
PPP1R15B	miRNA target sites

Extended variants
information (count: 2191 )
Associated
traits (count: 92 )

Variant overlapped rSNPs/rCNVs (count:2191 , 50 per page) page: 1 2 3 4 5 6 7 ... 44

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs201965734	chr1:46969641-46969642	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs527911385	chr1:46969652-46969653	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs552726322	chr1:46969653-46969654	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs534145955	chr1:46969655-46969656	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs371340038	chr1:46969657-46969658	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs187884040	chr1:46969678-46969679	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs191000411	chr1:46969681-46969682	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs568528663	chr1:46969686-46969687	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs74802410	chr1:46969687-46969688	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs182765985	chr1:46969715-46969716	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs376200463	chr1:46969766-46969767	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs566547757	chr1:46969891-46969892	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs374449607	chr1:46969894-46969895	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs369671491	chr1:46969943-46969944	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs558716512	chr1:46969960-46969961	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs576919797	chr1:46970001-46970002	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs538149576	chr1:46970004-46970005	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs556465191	chr1:46970013-46970014	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs574912208	chr1:46970101-46970102	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs542225653	chr1:46970104-46970105	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs560606944	chr1:46970105-46970106	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs572497562	chr1:46970259-46970260	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs545929381	chr1:46970297-46970298	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs35452063	chr1:46970400-46970401	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs36074980	chr1:46970428-46970429	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs564710670	chr1:46970648-46970649	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs373283193	chr1:46970677-46970678	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs188088569	chr1:46970716-46970717	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs61783063	chr1:46970766-46970767	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs61783064	chr1:46970790-46970791	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs531777259	chr1:46970865-46970866	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs200424051	chr1:46970985-46970986	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs562022920	chr1:46971003-46971004	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs529675595	chr1:46971020-46971021	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs55929143	chr1:46971165-46971166	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs370276856	chr1:46971189-46971190	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs376046881	chr1:46971279-46971280	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs558250569	chr1:46971289-46971290	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs11803425	chr1:46971342-46971343	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs61783065	chr1:46971369-46971370	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs570644829	chr1:46971372-46971373	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs538014227	chr1:46971429-46971430	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs192731676	chr1:46971431-46971432	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs546381652	chr1:46971442-46971443	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs71572613	chr1:46971458-46971459	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs398049252	chr1:46971471-46971472	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs115473181	chr1:46971482-46971483	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs75120915	chr1:46971555-46971556	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs373742511	chr1:46971564-46971565	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs554137653	chr1:46971612-46971613	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:92)

Disease	PMID	Source
Glioblastoma multiforme	21080181	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	17603634	CNVD
Soft tissue tumor	16732325	CNVD
Papillary thyroid carcinoma	21436994	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Colorectal cancer	16272173	CNVD
Wilms tumour	21544195	CNVD
Coronary Disease	20032323	CNVD
Prostate cancer	21965145	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Stargardt''s disease	17277736	CNVD
Neuroblastoma	17897457	CNVD
Uveal melanoma	21693616	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	21484798	CNVD
Non-syndromic sensorineural hearing loss	22290220	CNVD
Liposarcoma	21253554	CNVD
Breast cancer	21264507	CNVD
Acute myeloid leukemia	16864856	CNVD
Astrocytoma	17387387	CNVD
Cancer	21499728	CNVD
Glioblastoma multiforme	17387387	CNVD
Oligodendroglial tumors	17285580	CNVD
Neuroblastoma	17535989	CNVD
Pheochromocytoma	17535989	CNVD
Prostate cancer	16705090	CNVD
Astrocytoma	17934521	CNVD
Colorectal cancer	19359472	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Neuroblastoma	17533364	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Chronic myeloid leukemia	21384125	CNVD
Prostate cancer	18632612	CNVD
Autism	22495311	CNVD
Non-small cell lung cancer	21385341	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Chordoma	21602918	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Melanoma	18172304	CNVD
Multiple myeloma	16461302	CNVD
Melanoma	17363583	CNVD
Cancer	21129771	CNVD
Autosomal dominant nocturnal frontal lobe epilepsy	18472482	CNVD
Hirschsprung''s Disease	21712996	CNVD
Non-small cell lung cancer	20864512	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Thrombocytopenia-absent radius syndrome	21933853	CNVD
Psychiatric disorder	22848183	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	20409316	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Lung cancer	18438408	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17393978	CNVD
Cervical cancer	21062161	CNVD
Cancer	21183584	CNVD
Muscle-eye-brain disease	21572526	CNVD
Breast cancer	21785460	CNVD
Myelofibrosis	22110671	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21364760	CNVD
Neuroblastoma	21899760	CNVD
Uveal melanoma	20484589	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Glioblastoma	20031968	CNVD
Leukemia	18688285	CNVD
Rett syndrome	21593744	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:1414 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:46969400-46972600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr1:46969600-46971400	Weak transcription	K562	blood
3	chr1:46969600-46972600	Weak transcription	Right Atrium	heart
4	chr1:46971400-46975600	Enhancers	K562	blood
5	chr1:46972200-46973200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
6	chr1:46972200-46973200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
7	chr1:46972600-46972800	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell
8	chr1:46972600-46972800	Flanking Active TSS	Cortex derived primary cultured neurospheres	brain
9	chr1:46972600-46972800	Strong transcription	Right Atrium	heart
10	chr1:46972600-46973000	Enhancers	H1 Cell Line	embryonic stem cell
11	chr1:46972600-46973000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
12	chr1:46972600-46973000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
13	chr1:46972600-46973200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
14	chr1:46972600-46973200	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
15	chr1:46972600-46973400	Bivalent Enhancer	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
16	chr1:46972600-46974000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
17	chr1:46972600-46974200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
18	chr1:46972800-46973200	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell
19	chr1:46972800-46973200	Enhancers	iPS-18 Cell Line	embryonic stem cell
20	chr1:46972800-46974000	Enhancers	Cortex derived primary cultured neurospheres	brain
21	chr1:46972800-46986000	Weak transcription	Right Atrium	heart
22	chr1:46973000-46974000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
23	chr1:46973000-46977200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
24	chr1:46973200-46975200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
25	chr1:46973800-46974000	Bivalent Enhancer	Fetal Muscle Trunk	muscle
26	chr1:46974000-46974400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
27	chr1:46974400-46976000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
28	chr1:46974600-46974800	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
29	chr1:46974800-46975400	Enhancers	Osteobl	bone
30	chr1:46975200-46975400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
31	chr1:46976000-46979600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
32	chr1:46976600-46977000	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin01	Skin
33	chr1:46976600-46978400	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
34	chr1:46976800-46977800	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
35	chr1:46976800-46979400	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell
36	chr1:46976800-46979400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
37	chr1:46977000-46977200	Bivalent Enhancer	ES-I3 Cell Line	embryonic stem cell
38	chr1:46977000-46978400	Bivalent Enhancer	ES-WA7 Cell Line	embryonic stem cell
39	chr1:46977200-46977400	Bivalent Enhancer	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
40	chr1:46977200-46977800	Bivalent Enhancer	HUES64 Cell Line	embryonic stem cell
41	chr1:46977200-46977800	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
42	chr1:46977200-46978200	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin01	Skin
43	chr1:46977200-46979200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
44	chr1:46977400-46977800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
45	chr1:46977600-46978400	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell
46	chr1:46977800-46981800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
47	chr1:46978600-46979400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
48	chr1:46978800-46979200	Bivalent Enhancer	ES-I3 Cell Line	embryonic stem cell
49	chr1:46979000-46979200	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
50	chr1:46979000-46979400	Bivalent Enhancer	HepG2	liver

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