Variant report

Variant	nsv1045367
Chromosome Location	chr15:99781626-99892182
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2021)
CpG islands
(count:1221)
Chromatin interactive
region (count:56)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:1)

(count:2021 , 50 per page) page: 1 2 3 4 5 6 7 ... 41

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr15:99852295-99853142	K562	blood:	n/a	n/a
2	ARID3A	chr15:99846228-99846789	HepG2	liver:	n/a	chr15:99846306-99846322
3	ARID3A	chr15:99813243-99813446	K562	blood:	n/a	n/a
4	ARID3A	chr15:99883375-99883659	HepG2	liver:	n/a	n/a
5	ARID3A	chr15:99790922-99791899	HepG2	liver:	n/a	n/a
6	ARID3A	chr15:99880457-99880856	HepG2	liver:	n/a	chr15:99880645-99880661
7	ARID3A	chr15:99826755-99826938	HepG2	liver:	n/a	n/a
8	ARID3A	chr15:99791850-99792363	K562	blood:	n/a	n/a
9	ARID3A	chr15:99797553-99797840	HepG2	liver:	n/a	n/a
10	ARID3A	chr15:99808749-99809017	HepG2	liver:	n/a	n/a
11	ATF1	chr15:99798217-99798327	K562	blood:	n/a	n/a
12	ATF1	chr15:99791001-99791616	K562	blood:	n/a	n/a
13	ATF1	chr15:99850971-99851292	K562	blood:	n/a	n/a
14	ATF1	chr15:99829160-99829174	K562	blood:	n/a	n/a
15	ATF1	chr15:99813211-99813447	K562	blood:	n/a	n/a
16	ATF1	chr15:99864437-99864834	K562	blood:	n/a	n/a
17	ATF1	chr15:99852443-99852972	K562	blood:	n/a	n/a
18	ATF2	chr15:99791049-99791639	GM12878	blood:	n/a	n/a
19	ATF2	chr15:99864341-99864893	GM12878	blood:	n/a	n/a
20	ATF2	chr15:99864284-99864957	GM12878	blood:	n/a	n/a
21	ATF2	chr15:99791241-99791627	H1-hESC	embryonic stem cell:	n/a	n/a
22	ATF2	chr15:99790825-99791768	GM12878	blood:	n/a	n/a
23	ATF2	chr15:99791342-99791717	H1-hESC	embryonic stem cell:	n/a	n/a
24	ATF3	chr15:99864085-99864956	A549	lung:	n/a	n/a
25	ATF3	chr15:99864139-99865019	HCT-116	colon:	n/a	n/a
26	ATF3	chr15:99863947-99864628	A549	lung:	n/a	n/a
27	ATF3	chr15:99790726-99791552	A549	lung:	n/a	n/a
28	BACH1	chr15:99792247-99792257	K562	blood:	n/a	n/a
29	BACH1	chr15:99791217-99792087	H1-hESC	embryonic stem cell:	n/a	n/a
30	BACH1	chr15:99856134-99856158	H1-hESC	embryonic stem cell:	n/a	n/a
31	BATF	chr15:99888611-99888876	GM12878	blood:	n/a	n/a
32	BATF	chr15:99864228-99864489	GM12878	blood:	n/a	chr15:99864364-99864375
33	BATF	chr15:99888678-99888879	GM12878	blood:	n/a	n/a
34	BCL3	chr15:99864031-99864882	A549	lung:	n/a	n/a
35	BCL3	chr15:99790815-99791656	A549	lung:	n/a	n/a
36	BCL3	chr15:99790928-99791629	A549	lung:	n/a	n/a
37	BCL3	chr15:99863946-99865300	A549	lung:	n/a	n/a
38	BCLAF1	chr15:99826592-99827059	GM12878	blood:	n/a	n/a
39	BCLAF1	chr15:99790674-99791521	GM12878	blood:	n/a	n/a
40	BCLAF1	chr15:99790744-99791594	GM12878	blood:	n/a	n/a
41	BCLAF1	chr15:99864343-99864871	GM12878	blood:	n/a	n/a
42	BHLHE40	chr15:99813351-99813378	K562	blood:	n/a	n/a
43	BHLHE40	chr15:99884108-99884275	HepG2	liver:	n/a	n/a
44	BHLHE40	chr15:99850957-99851553	K562	blood:	n/a	n/a
45	BHLHE40	chr15:99880229-99880429	K562	blood:	n/a	n/a
46	BHLHE40	chr15:99852526-99852941	K562	blood:	n/a	n/a
47	BHLHE40	chr15:99790978-99792068	K562	blood:	n/a	chr15:99791430-99791446
48	BHLHE40	chr15:99791121-99791990	GM12878	blood:	n/a	chr15:99791430-99791446
49	BRCA1	chr15:99791015-99791880	Hela-S3	cervix:	n/a	n/a
50	BRCA1	chr15:99789357-99790269	Hela-S3	cervix:	n/a	n/a

(count:1221 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:99789661-99789711	HRCEpiC	kidney:	n/a
2	chr15:99789661-99789711	HRCEpiC	kidney:	n/a
3	chr15:99790901-99790951	HRCEpiC	kidney:	n/a
4	chr15:99791569-99791619	RPTEC	kidney:	n/a
5	chr15:99791496-99791546	HEK293	kidney:	embryo
6	chr15:99789777-99789827	HMEC	breast:	n/a
7	chr15:99789637-99789687	HUVEC	blood vessel:	n/a
8	chr15:99795399-99795449	AG04449	skin:	fetal
9	chr15:99791485-99791535	HEK293	kidney:	embryo
10	chr15:99789855-99789905	GM12891	blood:	n/a
11	chr15:99791496-99791546	H1-hESC	embryonic stem cell:	embryo
12	chr15:99791508-99791558	HRCEpiC	kidney:	n/a
13	chr15:99789622-99789672	NH-A	brain:	n/a
14	chr15:99791282-99791332	RPTEC	kidney:	n/a
15	chr15:99791508-99791558	HepG2	liver:	n/a
16	chr15:99792144-99792194	BJ	skin:	n/a
17	chr15:99864059-99864109	GM19239	blood:	n/a
18	chr15:99789637-99789687	PFSK-1	brain:	n/a
19	chr15:99791485-99791535	Hela-S3	cervix:	n/a
20	chr15:99791485-99791535	Caco-2	colon:	n/a
21	chr15:99864059-99864109	Hepatocyte	liver:	n/a
22	chr15:99791282-99791332	HMEC	breast:	n/a
23	chr15:99789777-99789827	HIPEpiC	eye:	n/a
24	chr15:99789777-99789827	HPAEpiC	pulmonary alveolar:	n/a
25	chr15:99791336-99791386	K562	blood:	n/a
26	chr15:99789855-99789905	NHBE	bronchial:	n/a
27	chr15:99789661-99789711	NB4	blood:	n/a
28	chr15:99791569-99791619	BE2_C	brain:	n/a
29	chr15:99789622-99789672	H1-hESC	embryonic stem cell:	embryo
30	chr15:99791485-99791535	CMK	blood:	n/a
31	chr15:99791569-99791619	A549	lung:	n/a
32	chr15:99792144-99792194	U87	brain:	n/a
33	chr15:99791496-99791546	HepG2	liver:	n/a
34	chr15:99792144-99792194	AG04449	skin:	fetal
35	chr15:99789637-99789687	SK-N-SH	brain:	n/a
36	chr15:99789637-99789687	HRPEpiC	eye:	n/a
37	chr15:99789622-99789672	GM12878	blood:	n/a
38	chr15:99788558-99788608	GM06990	blood:	n/a
39	chr15:99791508-99791558	K562	blood:	n/a
40	chr15:99836575-99836625	IMR90	lung:	fetal
41	chr15:99790901-99790951	AG04450	lung:	fetal
42	chr15:99791546-99791596	SKMC	muscle:	n/a
43	chr15:99791485-99791535	HCPEpiC	choroid plexus:	n/a
44	chr15:99789777-99789827	HCT-116	colon:	n/a
45	chr15:99790901-99790951	NT2-D1	testis:	n/a
46	chr15:99791282-99791332	HEK293	kidney:	embryo
47	chr15:99791546-99791596	Hela-S3	cervix:	n/a
48	chr15:99795399-99795449	MCF10A-Er-Src	breast:	n/a
49	chr15:99791336-99791386	Hela-S3	cervix:	n/a
50	chr15:99791109-99791159	GM12878	blood:	n/a

(count:56 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr15:45003258..45003898-chr15:99790871..99791766,2	NB4	blood:
2	chr15:99791130..99791720-chr17:41465594..41466467,2	Hela-S3	cervix:
3	chr15:99789846..99791808-chr15:100272487..100274799,2	MCF-7	breast:
4	chr15:99788127..99791108-chr15:99792243..99793962,2	K562	blood:
5	chr15:99791300..99794285-chr15:99798721..99800765,2	K562	blood:
6	chr15:99813138..99813798-chr15:100269841..100270582,3	MCF-7	breast:
7	chr15:99856389..99859314-chr15:99863031..99866195,3	MCF-7	breast:
8	chr15:99846877..99849995-chr15:99854925..99857345,3	MCF-7	breast:
9	chr15:99807323..99810075-chr15:100272302..100274258,2	MCF-7	breast:
10	chr15:99856565..99859133-chr15:99884132..99886600,2	MCF-7	breast:
11	chr15:99813197..99813935-chr20:33427071..33428071,2	MCF-7	breast:
12	chr15:99882409..99885385-chr15:99887042..99889200,2	MCF-7	breast:
13	chr15:99884303..99885875-chr15:99888389..99890129,2	K562	blood:
14	chr15:99820578..99822487-chr15:99824198..99826248,2	MCF-7	breast:
15	chr15:99791079..99791792-chr22:24236535..24237112,2	HCT-116	colon:
16	chr15:99777851..99781932-chr15:99788506..99792058,4	MCF-7	breast:
17	chr1:37939783..37940413-chr15:99790980..99791738,2	Hela-S3	cervix:
18	chr15:99784175..99787630-chr15:99790166..99793752,4	K562	blood:
19	chr15:99812878..99813498-chr15:100243248..100244206,2	MCF-7	breast:
20	chr15:99889586..99891460-chr15:99894406..99897341,2	K562	blood:
21	chr15:99790531..99793156-chr15:100244093..100247016,2	MCF-7	breast:
22	chr15:99856389..99859314-chr15:99863031..99866195,3	MCF-7	breast:
23	chr15:99776229..99778768-chr15:99786778..99789073,2	K562	blood:
24	chr15:99846877..99849995-chr15:99854925..99857345,3	MCF-7	breast:
25	chr15:99788127..99790475-chr15:99792462..99794073,2	K562	blood:
26	chr15:99647521..99649996-chr15:99837108..99838795,2	MCF-7	breast:
27	chr15:99791782..99793591-chr15:99794191..99796456,2	K562	blood:
28	chr15:99804185..99806716-chr15:99808711..99810346,2	MCF-7	breast:
29	chr12:45609214..45609830-chr15:99790871..99791410,2	NB4	blood:
30	chr15:99826798..99828339-chr15:100272977..100274878,2	MCF-7	breast:
31	chr15:99790997..99791604-chr17:79368586..79369422,2	HCT-116	colon:
32	chr15:99883899..99884477-chr15:100244392..100244959,2	MCF-7	breast:
33	chr15:99875104..99877834-chr15:99882696..99885261,2	K562	blood:
34	chr15:99856565..99859133-chr15:99884132..99886600,2	MCF-7	breast:
35	chr15:99790234..99792055-chr2:242088635..242090209,2	MCF-7	breast:
36	chr15:99812901..99813825-chr15:100295748..100296397,4	K562	blood:
37	chr15:99643812..99646594-chr15:99789555..99792592,4	MCF-7	breast:
38	chr15:99883235..99885875-chr15:99888389..99889955,2	K562	blood:
39	chr15:99882409..99885385-chr15:99887042..99889200,2	MCF-7	breast:
40	chr15:99875104..99877834-chr15:99882696..99885261,2	K562	blood:
41	chr15:99644709..99645388-chr15:99791744..99792284,2	MCF-7	breast:
42	chr15:99828116..99830742-chr15:99902664..99904284,2	MCF-7	breast:
43	chr15:99826876..99828722-chr15:100104864..100106375,2	MCF-7	breast:
44	chr15:99845791..99847734-chr15:99849228..99852501,3	K562	blood:
45	chr15:99812628..99814196-chr15:100244285..100245248,5	K562	blood:
46	chr15:99883235..99885875-chr15:99888389..99889955,2	K562	blood:
47	chr15:99884303..99885875-chr15:99888389..99890129,2	K562	blood:
48	chr15:99762009..99765655-chr15:99790108..99792308,4	MCF-7	breast:
49	chr15:99846693..99847599-chr2:219395068..219395705,2	MCF-7	breast:
50	chr15:99788657..99793033-chr15:100273651..100276844,5	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-MEF2A-7	chr15:99848897-99851046	l_1246_chr15:99847899-99851046_liver
2	lnc-MEF2A-6	chr15:99878062-99878686	NONHSAT050865
3	lnc-MEF2A-7	chr15:99847900-99848768	l_1246_chr15:99847899-99851046_liver

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	LRRC28	hsa-miR-34a-5p	chr15:99874260-99874282

Variant related genes	Relation type
ENSG00000264771	TF binding region
LRRC28	TF binding region
HSP90B2P	TF binding region
HNRNPA1P62	TF binding region
ENSG00000268730	TF binding region
ENSG00000259257	TF binding region
TTC23	TF binding region
ENSG00000264771	CpG island
LRRC28	CpG island
HSP90B2P	CpG island
HNRNPA1P62	CpG island
ENSG00000268730	CpG island
ENSG00000259257	CpG island
TTC23	CpG island
ENSG00000115685	chromatin interactions
ENSG00000263053	chromatin interactions
ENSG00000103852	chromatin interactions
ENSG00000259228	chromatin interactions
ENSG00000134297	chromatin interactions
ENSG00000163874	chromatin interactions
ENSG00000166710	chromatin interactions
ENSG00000177119	chromatin interactions
ENSG00000115687	chromatin interactions
ENSG00000188825	chromatin interactions
ENSG00000197903	chromatin interactions
ENSG00000233621	chromatin interactions
ENSG00000184825	chromatin interactions
ENSG00000221511	chromatin interactions
ENSG00000168904	chromatin interactions
ENSG00000183060	chromatin interactions
ENSG00000229474	chromatin interactions
ENSG00000068305	chromatin interactions
ENSG00000240972	chromatin interactions
ENSG00000259475	chromatin interactions
ENSG00000182253	chromatin interactions

Extended variants
information (count: 4226 )
Associated
traits (count: 68 )

Variant overlapped rSNPs/rCNVs (count:4226 , 50 per page) page: 1 2 3 4 5 6 7 ... 85

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs144532592	chr15:99781775-99781776	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs574315106	chr15:99781816-99781817	Strong transcription Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs182222545	chr15:99781827-99781828	Strong transcription Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs62025702	chr15:99781841-99781842	Strong transcription Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs186650386	chr15:99781855-99781856	Strong transcription Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs148462764	chr15:99781934-99781935	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs142838044	chr15:99781964-99781965	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs192670853	chr15:99782052-99782053	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs146103434	chr15:99782067-99782068	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs184655258	chr15:99782110-99782111	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs72756894	chr15:99782112-99782113	Strong transcription Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs117073787	chr15:99782146-99782147	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs568803578	chr15:99782169-99782170	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs532825588	chr15:99782176-99782177	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs551481210	chr15:99782183-99782184	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs566618657	chr15:99782196-99782197	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs534384105	chr15:99782209-99782210	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs555957071	chr15:99782240-99782241	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs140023286	chr15:99782241-99782242	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs75401770	chr15:99782254-99782255	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs188775971	chr15:99782291-99782292	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs35988389	chr15:99782339-99782340	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs1223951	chr15:99782387-99782388	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
24	rs577952575	chr15:99782444-99782445	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs143540336	chr15:99782446-99782447	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs12911898	chr15:99782595-99782596	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
27	rs192949297	chr15:99782611-99782612	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs199866805	chr15:99782661-99782662	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs1223950	chr15:99782662-99782663	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs368967686	chr15:99782703-99782704	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs561895019	chr15:99782929-99782930	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs529094979	chr15:99782993-99782994	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs544480696	chr15:99782994-99782995	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs34693158	chr15:99783001-99783002	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs185144762	chr15:99783030-99783031	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs553544192	chr15:99783048-99783049	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs189610865	chr15:99783074-99783075	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs567470050	chr15:99783075-99783076	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs181267753	chr15:99783077-99783078	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs34375755	chr15:99783115-99783116	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs551437007	chr15:99783118-99783119	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs376451341	chr15:99783126-99783127	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs372467955	chr15:99783178-99783179	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs566482544	chr15:99783196-99783197	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs527334549	chr15:99783224-99783225	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
46	rs151250637	chr15:99783251-99783252	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
47	rs567811992	chr15:99783254-99783255	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
48	rs538088411	chr15:99783278-99783279	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
49	rs550425313	chr15:99783281-99783282	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
50	rs571891094	chr15:99783314-99783315	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:68)

Disease	PMID	Source
Ewing''s sarcoma	21437220	CNVD
Schizophrenia	19415332	CNVD
Breast cancer	22522925	CNVD
Wilms tumour	21544195	CNVD
cataract	16735990	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Medulloblastoma	21979893	CNVD
spastic paraplegia with thinning of corpus callosum	19105190	CNVD
Schizophrenia	21324950	CNVD
Astrocytoma	17387387	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Disease	21824424	CNVD
Melanoma	18172304	CNVD
Gastric cancer	17167181	CNVD
Neuroblastoma	19435921	CNVD
Colorectal cancer	19359472	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Colorectal cancer	16272173	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Multiple myeloma	17550852	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute myeloid leukemia	20729466	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Multiple myeloma	20724749	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Cancer	16751803	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Lung cancer	18438408	CNVD
Acute myeloid leukemia	16864856	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
small cell lung cancer	20016488	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Sudden cardiac death	19188705	CNVD
Intellectual disability	22102821	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Ovarian cancer	21720365	CNVD
Developmental delay	21147756	CNVD
Hepatocellular carcinoma	16750200	CNVD
Central neurocytomas	17123091	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Burkitt''s lymphoma	19759907	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Breast cancer	17133270	CNVD
Myelofibrosis	22110671	CNVD
Mental retardation	20811773	CNVD
Glioblastoma multiforme	22286061	CNVD
Breast cancer	21364760	CNVD
Breast cancer	20409316	CNVD
Emphysema	19352772	CNVD
Pilocytic astrocytoma	18622384	CNVD
Pilomyxoid astrocytoma	18622384	CNVD
Prostate cancer	18632612	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Breast cancer	17142309	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Renal cell carcinoma	21215367	CNVD
Schizophrenia	23813976	CNVD

Chromatin state (count:2363 , 50 per page) page: 1 2 3 4 5 6 7 ... 48

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:99673200-99789400	Weak transcription	Small Intestine	intestine
2	chr15:99733400-99787400	Weak transcription	NHEK	skin
3	chr15:99749800-99789400	Weak transcription	Brain Cingulate Gyrus	brain
4	chr15:99750000-99789400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
5	chr15:99756600-99789400	Weak transcription	Monocytes-CD14+_RO01746	blood
6	chr15:99758600-99789400	Weak transcription	Brain Substantia Nigra	brain
7	chr15:99759200-99788400	Weak transcription	Fetal Thymus	thymus
8	chr15:99759400-99781800	Weak transcription	Spleen	Spleen
9	chr15:99759400-99788600	Weak transcription	H9 Cell Line	embryonic stem cell
10	chr15:99759400-99788600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
11	chr15:99761400-99781800	Weak transcription	Pancreas	Pancrea
12	chr15:99761400-99788400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
13	chr15:99762600-99789400	Weak transcription	Gastric	stomach
14	chr15:99765400-99784000	Weak transcription	Hela-S3	cervix
15	chr15:99765600-99789400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
16	chr15:99765800-99789400	Weak transcription	Lung	lung
17	chr15:99768200-99788600	Weak transcription	Colonic Mucosa	Colon
18	chr15:99768200-99789200	Weak transcription	Brain Hippocampus Middle	brain
19	chr15:99768600-99787200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
20	chr15:99768600-99787200	Weak transcription	Duodenum Mucosa	Duodenum
21	chr15:99768600-99787200	Weak transcription	Skeletal Muscle Male	skeletal muscle
22	chr15:99768600-99787200	Weak transcription	HepG2	liver
23	chr15:99768600-99788400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
24	chr15:99768600-99788400	Weak transcription	Ovary	ovary
25	chr15:99768800-99783200	Weak transcription	Fetal Heart	heart
26	chr15:99768800-99787400	Weak transcription	Colon Smooth Muscle	Colon
27	chr15:99768800-99787400	Weak transcription	Rectal Smooth Muscle	rectum
28	chr15:99768800-99788200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
29	chr15:99768800-99788200	Weak transcription	NHLF	lung
30	chr15:99768800-99789400	Weak transcription	Sigmoid Colon	Sigmoid Colon
31	chr15:99769000-99787200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
32	chr15:99769000-99787400	Weak transcription	NHDF-Ad	bronchial
33	chr15:99769000-99788400	Weak transcription	HSMMtube	muscle
34	chr15:99769000-99788400	Weak transcription	NH-A	brain
35	chr15:99769200-99788200	Weak transcription	Fetal Kidney	kidney
36	chr15:99770200-99787400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
37	chr15:99773400-99788400	Weak transcription	HUES64 Cell Line	embryonic stem cell
38	chr15:99773600-99788400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
39	chr15:99773600-99788400	Weak transcription	HUES6 Cell Line	embryonic stem cell
40	chr15:99775000-99781800	Strong transcription	Fetal Lung	lung
41	chr15:99775400-99784400	Weak transcription	HSMM	muscle
42	chr15:99776600-99788800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
43	chr15:99777000-99788400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
44	chr15:99777800-99782000	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
45	chr15:99778400-99782200	Strong transcription	Fetal Muscle Leg	muscle
46	chr15:99778600-99782200	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
47	chr15:99778800-99788400	Weak transcription	Primary hematopoietic stem cells	blood
48	chr15:99779400-99787200	Weak transcription	Muscle Satellite Cultured Cells	--
49	chr15:99779800-99782200	Strong transcription	Fetal Muscle Trunk	muscle
50	chr15:99780000-99781800	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin

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