Variant report

Variant	nsv830603
Chromosome Location	chr1:93003657-93172206
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1048)
CpG islands
(count:61)
Chromatin interactive
region (count:37)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1048 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:93003665-93003865	HepG2	liver:	n/a	n/a
2	ARID3A	chr1:93170866-93171250	K562	blood:	n/a	n/a
3	ARID3A	chr1:93166804-93167004	K562	blood:	n/a	n/a
4	ARID3A	chr1:93010203-93010659	K562	blood:	n/a	n/a
5	ARID3A	chr1:93120890-93121035	HepG2	liver:	n/a	n/a
6	ARID3A	chr1:93166432-93166438	K562	blood:	n/a	n/a
7	ARID3A	chr1:93088811-93089050	K562	blood:	n/a	n/a
8	ATF1	chr1:93010226-93010719	K562	blood:	n/a	n/a
9	ATF1	chr1:93147755-93147985	K562	blood:	n/a	n/a
10	ATF1	chr1:93088911-93089075	K562	blood:	n/a	n/a
11	ATF1	chr1:93166705-93166957	K562	blood:	n/a	n/a
12	ATF2	chr1:93003504-93004675	GM12878	blood:	n/a	n/a
13	ATF2	chr1:93003523-93004631	GM12878	blood:	n/a	n/a
14	ATF2	chr1:93049835-93050460	GM12878	blood:	n/a	n/a
15	ATF2	chr1:93052940-93053482	GM12878	blood:	n/a	n/a
16	ATF2	chr1:93049269-93049816	GM12878	blood:	n/a	n/a
17	ATF2	chr1:93049329-93050426	GM12878	blood:	n/a	n/a
18	ATF2	chr1:93052866-93053483	GM12878	blood:	n/a	n/a
19	ATF2	chr1:93028878-93029464	GM12878	blood:	n/a	n/a
20	ATF3	chr1:93010277-93010640	K562	blood:	n/a	n/a
21	BACH1	chr1:93119744-93119935	K562	blood:	n/a	n/a
22	BACH1	chr1:93167070-93167279	K562	blood:	n/a	n/a
23	BATF	chr1:93049920-93050305	GM12878	blood:	n/a	chr1:93050185-93050195
24	BATF	chr1:93053051-93053397	GM12878	blood:	n/a	n/a
25	BATF	chr1:93157496-93157732	GM12878	blood:	n/a	n/a
26	BATF	chr1:93003587-93003947	GM12878	blood:	n/a	n/a
27	BATF	chr1:93049462-93049729	GM12878	blood:	n/a	n/a
28	BATF	chr1:93050000-93050266	GM12878	blood:	n/a	chr1:93050185-93050195
29	BATF	chr1:93085113-93085316	GM12878	blood:	n/a	chr1:93085164-93085175
30	BATF	chr1:93004217-93004611	GM12878	blood:	n/a	n/a
31	BATF	chr1:93075641-93075836	GM12878	blood:	n/a	chr1:93075720-93075731
32	BATF	chr1:93004020-93004631	GM12878	blood:	n/a	n/a
33	BATF	chr1:93053049-93053391	GM12878	blood:	n/a	n/a
34	BATF	chr1:93157523-93157814	GM12878	blood:	n/a	n/a
35	BCL11A	chr1:93004234-93004554	GM12878	blood:	n/a	n/a
36	BCL11A	chr1:93053071-93053399	GM12878	blood:	n/a	n/a
37	BCL11A	chr1:93049426-93049685	GM12878	blood:	n/a	n/a
38	BCL11A	chr1:93049857-93050284	GM12878	blood:	n/a	chr1:93050184-93050193 chr1:93050234-93050241
39	BCL11A	chr1:93052959-93053476	GM12878	blood:	n/a	n/a
40	BCL11A	chr1:93049964-93050273	GM12878	blood:	n/a	chr1:93050184-93050193 chr1:93050234-93050241
41	BCL11A	chr1:93029038-93029400	GM12878	blood:	n/a	n/a
42	BCL11A	chr1:93004201-93004655	GM12878	blood:	n/a	n/a
43	BCL3	chr1:93052972-93053425	GM12878	blood:	n/a	n/a
44	BCL3	chr1:93049974-93050329	GM12878	blood:	n/a	chr1:93050184-93050193 chr1:93050234-93050241
45	BCLAF1	chr1:93049800-93050322	GM12878	blood:	n/a	chr1:93050184-93050193 chr1:93050234-93050241
46	BCLAF1	chr1:93049895-93050287	GM12878	blood:	n/a	chr1:93050184-93050193 chr1:93050234-93050241
47	BCLAF1	chr1:93028991-93029470	GM12878	blood:	n/a	n/a
48	BCLAF1	chr1:93053056-93053449	GM12878	blood:	n/a	n/a
49	BHLHE40	chr1:93003536-93004537	GM12878	blood:	n/a	n/a
50	BHLHE40	chr1:93147752-93148026	K562	blood:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:93101184-93101234	NT2-D1	testis:	n/a
2	chr1:93101184-93101234	HL-60	blood:	n/a
3	chr1:93101184-93101234	AG09309	skin:	n/a
4	chr1:93101184-93101234	NB4	blood:	n/a
5	chr1:93101184-93101234	ECC-1	luminal epithelium:	n/a
6	chr1:93101184-93101234	SAEC	small airway:	n/a
7	chr1:93101184-93101234	HNPCEpiC	eye:	n/a
8	chr1:93101184-93101234	AoSMC	blood vessel:	n/a
9	chr1:93101184-93101234	SK-N-SH	brain:	n/a
10	chr1:93101184-93101234	AG04449	skin:	fetal
11	chr1:93101184-93101234	SKMC	muscle:	n/a
12	chr1:93101184-93101234	Hela-S3	cervix:	n/a
13	chr1:93101184-93101234	MCF-7	breast:	n/a
14	chr1:93101184-93101234	PANC-1	pancreas:	n/a
15	chr1:93101184-93101234	AG09319	gingival:	n/a
16	chr1:93101184-93101234	HRCEpiC	kidney:	n/a
17	chr1:93101184-93101234	MCF10A-Er-Src	breast:	n/a
18	chr1:93101184-93101234	U87	brain:	n/a
19	chr1:93101184-93101234	GM12891	blood:	n/a
20	chr1:93101184-93101234	SK-N-MC	brain:	n/a
21	chr1:93101184-93101234	GM12878	blood:	n/a
22	chr1:93101184-93101234	Hepatocyte	liver:	n/a
23	chr1:93101184-93101234	LNCaP	prostate:	n/a
24	chr1:93101184-93101234	PrEC	prostate:	n/a
25	chr1:93101184-93101234	HEK293	kidney:	embryo
26	chr1:93101184-93101234	ovcar-3	ovarian:	n/a
27	chr1:93101184-93101234	HIPEpiC	eye:	n/a
28	chr1:93101184-93101234	SK-N-SH_RA	brain:	n/a
29	chr1:93101184-93101234	ProgFib	skin:	n/a
30	chr1:93101184-93101234	H1-hESC	embryonic stem cell:	embryo
31	chr1:93101184-93101234	Jurkat	blood:	n/a
32	chr1:93101184-93101234	BJ	skin:	n/a
33	chr1:93101184-93101234	HRPEpiC	eye:	n/a
34	chr1:93101184-93101234	HAEpiC	amniotic membrane:	n/a
35	chr1:93101184-93101234	CMK	blood:	n/a
36	chr1:93101184-93101234	IMR90	lung:	fetal
37	chr1:93101184-93101234	NHBE	bronchial:	n/a
38	chr1:93101184-93101234	RPTEC	kidney:	n/a
39	chr1:93101184-93101234	HCT-116	colon:	n/a
40	chr1:93101184-93101234	HUVEC	blood vessel:	n/a
41	chr1:93101184-93101234	HEEpiC	esophagus:	n/a
42	chr1:93101184-93101234	PFSK-1	brain:	n/a
43	chr1:93101184-93101234	T-47D	breast:	n/a
44	chr1:93101184-93101234	HCPEpiC	choroid plexus:	n/a
45	chr1:93101184-93101234	HPAEpiC	pulmonary alveolar:	n/a
46	chr1:93101184-93101234	BE2_C	brain:	n/a
47	chr1:93101184-93101234	HMEC	breast:	n/a
48	chr1:93101184-93101234	HCF	heart:	n/a
49	chr1:93101184-93101234	A549	lung:	n/a
50	chr1:93101184-93101234	K562	blood:	n/a

(count:37 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:93167180..93169532-chr1:93173013..93175472,3	K562	blood:
2	chr1:92987883..92989891-chr1:93008621..93010399,2	K562	blood:
3	chr1:93037475..93039657-chr1:93040585..93042175,2	K562	blood:
4	chr1:93164366..93166063-chr1:93176534..93179501,2	K562	blood:
5	chr1:92762843..92765397-chr1:93103121..93105425,2	K562	blood:
6	chr1:93168714..93171281-chr1:93175586..93177919,2	K562	blood:
7	chr1:93110037..93112267-chr1:93116205..93118057,2	K562	blood:
8	chr1:93037475..93039657-chr1:93040585..93042175,2	K562	blood:
9	chr1:93125325..93128274-chr1:93138494..93140203,2	K562	blood:
10	chr1:93066748..93068619-chr1:93086339..93088517,2	K562	blood:
11	chr1:93119617..93122057-chr1:93123545..93126419,2	K562	blood:
12	chr1:93155607..93158060-chr1:93158648..93160493,3	K562	blood:
13	chr1:93119617..93122057-chr1:93123545..93126419,2	K562	blood:
14	chr1:93027014..93029326-chr1:93048258..93050872,2	K562	blood:
15	chr1:93038487..93040567-chr1:93043443..93045326,2	K562	blood:
16	chr1:93008775..93011605-chr1:93017435..93019676,2	K562	blood:
17	chr1:93109943..93111571-chr1:93248352..93250763,2	MCF-7	breast:
18	chr1:92775257..92776314-chr1:93064696..93065442,3	MCF-7	breast:
19	chr1:93165676..93168735-chr1:93171801..93174880,3	K562	blood:
20	chr1:93125325..93128274-chr1:93138494..93140203,2	K562	blood:
21	chr1:92762166..92764342-chr1:93135404..93137126,2	K562	blood:
22	chr1:93110037..93112267-chr1:93116205..93118057,2	K562	blood:
23	chr1:93038487..93040567-chr1:93043443..93045326,2	K562	blood:
24	chr1:93107293..93109350-chr1:93297737..93299752,2	K562	blood:
25	chr1:93072009..93073923-chr1:93074325..93077014,2	K562	blood:
26	chr1:93154026..93155990-chr1:93160380..93162982,2	K562	blood:
27	chr1:93134530..93136643-chr1:93142430..93144187,2	K562	blood:
28	chr1:93155607..93158060-chr1:93158648..93160493,3	K562	blood:
29	chr1:93072009..93073923-chr1:93074325..93077014,2	K562	blood:
30	chr1:93154026..93155990-chr1:93160380..93162982,2	K562	blood:
31	chr1:93027014..93029326-chr1:93048258..93050872,2	K562	blood:
32	chr1:93114313..93117003-chr1:93124509..93127384,2	K562	blood:
33	chr1:93066748..93068619-chr1:93086339..93088517,2	K562	blood:
34	chr1:93134641..93136643-chr1:93142209..93143930,2	K562	blood:
35	chr1:93008775..93011605-chr1:93017435..93019676,2	K562	blood:
36	chr1:92763317..92764881-chr1:93069205..93071027,2	K562	blood:
37	chr1:93114313..93117003-chr1:93124509..93127384,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FAM69A-2	chr1:93170112-93170301	NONHSAT004463
2	lnc-GFI1-2	chr1:93046033-93046378	NONHSAT004461
3	lnc-FAM69A-2	chr1:93169415-93169478	NONHSAT004463

No data

Variant related genes	Relation type
ENSG00000223787	TF binding region
EVI5	TF binding region
RNU4-59P	TF binding region
HMGB3P9	TF binding region
ENSG00000223787	CpG island
EVI5	CpG island
RNU4-59P	CpG island
HMGB3P9	CpG island
ENSG00000122484	chromatin interactions
ENSG00000122406	chromatin interactions
ENSG00000174842	chromatin interactions
ENSG00000201317	chromatin interactions
ENSG00000067208	chromatin interactions

Extended variants
information (count: 6412 )
Associated
traits (count: 105 )

Variant overlapped rSNPs/rCNVs (count:6412 , 50 per page) page: 1 2 3 4 5 6 7 ... 129

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs544851144	chr1:93003664-93003665	Enhancers Flanking Active TSS Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
2	rs560298299	chr1:93003666-93003667	Enhancers Flanking Active TSS Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs192157928	chr1:93003692-93003693	Enhancers Flanking Active TSS Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs34049819	chr1:93003712-93003713	Enhancers Flanking Active TSS Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs35199577	chr1:93003721-93003722	Enhancers Flanking Active TSS Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs542950542	chr1:93003733-93003734	Enhancers Flanking Active TSS Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs139209754	chr1:93003805-93003806	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs531360754	chr1:93003870-93003871	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs565443228	chr1:93003938-93003939	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs149950737	chr1:93003948-93003949	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs2151576	chr1:93003949-93003950	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs370208654	chr1:93003996-93003997	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs549885953	chr1:93004032-93004033	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs565569859	chr1:93004042-93004043	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs184937156	chr1:93004068-93004069	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs144681304	chr1:93004106-93004107	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs187907518	chr1:93004177-93004178	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs572594674	chr1:93004183-93004184	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs553863815	chr1:93004195-93004196	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs2151577	chr1:93004219-93004220	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs555685055	chr1:93004276-93004277	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs192266930	chr1:93004321-93004322	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs567523868	chr1:93004353-93004354	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs184513236	chr1:93004354-93004355	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs536659400	chr1:93004362-93004363	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs189618506	chr1:93004384-93004385	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs564329117	chr1:93004385-93004386	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs578002053	chr1:93004400-93004401	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs545493523	chr1:93004491-93004492	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs7513775	chr1:93004497-93004498	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
31	rs572252879	chr1:93004498-93004499	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs139829351	chr1:93004504-93004505	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs181947226	chr1:93004525-93004526	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs74101190	chr1:93004537-93004538	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs184734626	chr1:93004546-93004547	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs564877151	chr1:93004551-93004552	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs532066618	chr1:93004571-93004572	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs547507863	chr1:93004597-93004598	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs189540897	chr1:93004621-93004622	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs180741459	chr1:93004669-93004670	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs562970149	chr1:93004775-93004776	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs145493414	chr1:93004788-93004789	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs373593757	chr1:93004793-93004794	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs72964704	chr1:93004817-93004818	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs538154698	chr1:93004822-93004823	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs556099051	chr1:93004826-93004827	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs147692984	chr1:93004837-93004838	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs376623429	chr1:93004972-93004973	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs6658734	chr1:93004992-93004993	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs10735778	chr1:93005006-93005007	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:105)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Wilms tumour	21544195	CNVD
Coronary Disease	20032323	CNVD
Prostate cancer	21965145	CNVD
Glioblastoma multiforme	21080181	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
Papillary thyroid carcinoma	21436994	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
Breast cancer	17603634	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
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
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
Breast cancer	21785460	CNVD
Breast cancer	21364760	CNVD
Rett syndrome	21593744	CNVD
Prostate cancer	16573809	CNVD
Breast cancer	16608533	CNVD
Ovarian cancer	21720365	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Ewing''s sarcoma	17952124	CNVD
Cancer	22429812	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Breast cancer	17133270	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Multiple myeloma	17550852	CNVD
Breast cancer	16397240	CNVD
Esophageal adenocarcinoma	18820669	CNVD
small cell lung cancer	20016488	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Glioblastoma multiforme	21922591	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Myelofibrosis	22110671	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Prostate cancer	19156837	CNVD
Autism	17483303	CNVD
Malignant melanoma	17260012	CNVD
Lung adenocarcinoma	21935476	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Glioma	20126413	CNVD
Diamond-Blackfan anemia	22689679	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:1834 , 50 per page) page: 1 2 3 4 5 6 7 ... 37

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:92968200-93042800	Weak transcription	HSMM	muscle
2	chr1:92972600-93013400	Weak transcription	Ovary	ovary
3	chr1:92976400-93042400	Weak transcription	Fetal Stomach	stomach
4	chr1:92977600-93010600	Weak transcription	Sigmoid Colon	Sigmoid Colon
5	chr1:92977600-93013200	Weak transcription	Duodenum Smooth Muscle	Duodenum
6	chr1:92981800-93004000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
7	chr1:92981800-93033400	Weak transcription	NHEK	skin
8	chr1:92983600-93066200	Weak transcription	Adipose Nuclei	Adipose
9	chr1:92990800-93003800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
10	chr1:92993000-93007400	Weak transcription	Left Ventricle	heart
11	chr1:92993800-93007200	Weak transcription	Monocytes-CD14+_RO01746	blood
12	chr1:92994600-93066000	Weak transcription	Placenta	Placenta
13	chr1:92999400-93016600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
14	chr1:93001400-93004000	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
15	chr1:93001400-93024200	Weak transcription	Psoas Muscle	Psoas
16	chr1:93001600-93004600	Enhancers	Primary T killer naive cells fromperipheralblood	blood
17	chr1:93001600-93004600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
18	chr1:93001800-93004600	Enhancers	Primary hematopoietic stem cells short term culture	blood
19	chr1:93001800-93004600	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
20	chr1:93001800-93004600	Enhancers	HepG2	liver
21	chr1:93001800-93004800	Enhancers	HUVEC	blood vessel
22	chr1:93002200-93004200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
23	chr1:93002200-93004400	Enhancers	Primary hematopoietic stem cells	blood
24	chr1:93002200-93004800	Enhancers	NH-A	brain
25	chr1:93002400-93003800	Enhancers	Primary T helper naive cells fromperipheralblood	blood
26	chr1:93002400-93003800	Flanking Active TSS	Primary T regulatory cells fromperipheralblood	blood
27	chr1:93002400-93004000	Enhancers	Primary T helper cells PMA-I stimulated	--
28	chr1:93002400-93004800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
29	chr1:93002600-93003800	Enhancers	Muscle Satellite Cultured Cells	--
30	chr1:93002600-93004600	Enhancers	Osteobl	bone
31	chr1:93002800-93004000	Weak transcription	Primary B cells from peripheral blood	blood
32	chr1:93002800-93004000	Flanking Active TSS	Primary T cells from cord blood	blood
33	chr1:93002800-93004000	Weak transcription	Fetal Thymus	thymus
34	chr1:93002800-93004000	Weak transcription	Thymus	Thymus
35	chr1:93002800-93004800	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
36	chr1:93002800-93007400	Weak transcription	Primary monocytes fromperipheralblood	blood
37	chr1:93003400-93003800	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
38	chr1:93003400-93003800	Active TSS	Primary Natural Killer cells fromperipheralblood	blood
39	chr1:93003400-93003800	Enhancers	A549	lung
40	chr1:93003400-93003800	Flanking Active TSS	Dnd41	blood
41	chr1:93003400-93003800	Active TSS	GM12878-XiMat	blood
42	chr1:93003400-93004000	Active TSS	Primary T cells fromperipheralblood	blood
43	chr1:93003400-93004000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
44	chr1:93003400-93004200	Enhancers	Duodenum Mucosa	Duodenum
45	chr1:93003600-93003800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
46	chr1:93003600-93003800	Flanking Active TSS	Liver	Liver
47	chr1:93003600-93003800	Enhancers	Fetal Intestine Small	intestine
48	chr1:93003600-93004000	Active TSS	Primary T killer memory cells from peripheral blood	blood
49	chr1:93003600-93004000	Flanking Active TSS	Pancreatic Islets	Pancreatic Islet
50	chr1:93003600-93004400	Enhancers	Primary neutrophils fromperipheralblood	blood

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Variant report

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