Variant report

Variant	nsv1011338
Chromosome Location	chr1:144015838-144337917
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1407)
CpG islands
(count:61)
Chromatin interactive
region (count:5)
LncRNA
region (count:48)
Mature miRNA
region (count: 0)
miRNA target
sites (count:3)

(count:1407 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BATF	chr1:144157512-144157961	GM12878	blood:	n/a	chr1:144157741-144157749
2	BATF	chr1:144328845-144329056	GM12878	blood:	n/a	n/a
3	BATF	chr1:144333842-144334072	GM12878	blood:	n/a	n/a
4	BATF	chr1:144335102-144335314	GM12878	blood:	n/a	n/a
5	BATF	chr1:144036890-144037115	GM12878	blood:	n/a	n/a
6	BATF	chr1:144320981-144321799	GM12878	blood:	n/a	chr1:144321317-144321326
7	BATF	chr1:144067068-144067372	GM12878	blood:	n/a	chr1:144067195-144067206
8	BATF	chr1:144309943-144310144	GM12878	blood:	n/a	n/a
9	BATF	chr1:144322789-144323057	GM12878	blood:	n/a	n/a
10	BATF	chr1:144094411-144095211	GM12878	blood:	n/a	chr1:144094595-144094605
11	BATF	chr1:144068660-144069151	GM12878	blood:	n/a	chr1:144068921-144068932
12	BATF	chr1:144335044-144335280	GM12878	blood:	n/a	n/a
13	BATF	chr1:144326880-144327091	GM12878	blood:	n/a	n/a
14	BATF	chr1:144325736-144326116	GM12878	blood:	n/a	n/a
15	BATF	chr1:144314152-144314409	GM12878	blood:	n/a	n/a
16	BATF	chr1:144091634-144091915	GM12878	blood:	n/a	n/a
17	BATF	chr1:144333140-144333410	GM12878	blood:	n/a	n/a
18	BATF	chr1:144327210-144327464	GM12878	blood:	n/a	n/a
19	BATF	chr1:144146857-144147088	GM12878	blood:	n/a	n/a
20	BATF	chr1:144068682-144069090	GM12878	blood:	n/a	chr1:144068921-144068932
21	BATF	chr1:144336769-144337135	GM12878	blood:	n/a	n/a
22	BATF	chr1:144078682-144078883	GM12878	blood:	n/a	n/a
23	BATF	chr1:144327848-144328102	GM12878	blood:	n/a	n/a
24	BATF	chr1:144312324-144312589	GM12878	blood:	n/a	n/a
25	BATF	chr1:144094860-144095134	GM12878	blood:	n/a	n/a
26	BATF	chr1:144310931-144311678	GM12878	blood:	n/a	n/a
27	BATF	chr1:144157508-144157950	GM12878	blood:	n/a	chr1:144157741-144157749
28	BATF	chr1:144321363-144321837	GM12878	blood:	n/a	n/a
29	BATF	chr1:144328809-144329030	GM12878	blood:	n/a	n/a
30	BATF	chr1:144067020-144067334	GM12878	blood:	n/a	chr1:144067195-144067206
31	BATF	chr1:144310715-144311748	GM12878	blood:	n/a	n/a
32	BCL11A	chr1:144334777-144334967	GM12878	blood:	n/a	n/a
33	BCL11A	chr1:144320994-144321225	GM12878	blood:	n/a	n/a
34	BCL11A	chr1:144321339-144321783	GM12878	blood:	n/a	n/a
35	BCL11A	chr1:144333094-144333330	GM12878	blood:	n/a	n/a
36	BCL11A	chr1:144068678-144069120	GM12878	blood:	n/a	chr1:144068891-144068900
37	BCL11A	chr1:144314194-144314432	GM12878	blood:	n/a	n/a
38	BCL11A	chr1:144310610-144311577	GM12878	blood:	n/a	chr1:144311394-144311403
39	BCL11A	chr1:144158386-144158606	GM12878	blood:	n/a	n/a
40	BCL11A	chr1:144094857-144095137	GM12878	blood:	n/a	chr1:144094981-144094994
41	BCL11A	chr1:144326934-144327192	GM12878	blood:	n/a	n/a
42	BCL11A	chr1:144321366-144321847	GM12878	blood:	n/a	n/a
43	BCL11A	chr1:144314167-144314436	GM12878	blood:	n/a	n/a
44	BCL11A	chr1:144336247-144336448	GM12878	blood:	n/a	n/a
45	BCL11A	chr1:144322758-144322986	GM12878	blood:	n/a	n/a
46	BCL11A	chr1:144331015-144331313	GM12878	blood:	n/a	n/a
47	BCL11A	chr1:144067064-144067392	GM12878	blood:	n/a	chr1:144067198-144067207 chr1:144067199-144067208
48	BCL11A	chr1:144146512-144146801	GM12878	blood:	n/a	n/a
49	BCL11A	chr1:144320862-144321088	GM12878	blood:	n/a	n/a
50	BCL11A	chr1:144312312-144312566	GM12878	blood:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:144044138-144044188	HNPCEpiC	eye:	n/a
2	chr1:144044138-144044188	RPTEC	kidney:	n/a
3	chr1:144044138-144044188	AG09319	gingival:	n/a
4	chr1:144044138-144044188	HMEC	breast:	n/a
5	chr1:144044138-144044188	T-47D	breast:	n/a
6	chr1:144044138-144044188	Hepatocyte	liver:	n/a
7	chr1:144044138-144044188	HCM	heart:	n/a
8	chr1:144044138-144044188	GM06990	blood:	n/a
9	chr1:144044138-144044188	HRPEpiC	eye:	n/a
10	chr1:144044138-144044188	SK-N-SH	brain:	n/a
11	chr1:144044138-144044188	GM12878	blood:	n/a
12	chr1:144044138-144044188	K562	blood:	n/a
13	chr1:144044138-144044188	HCF	heart:	n/a
14	chr1:144044138-144044188	HepG2	liver:	n/a
15	chr1:144044138-144044188	SK-N-SH_RA	brain:	n/a
16	chr1:144044138-144044188	AG10803	skin:	n/a
17	chr1:144044138-144044188	HAEpiC	amniotic membrane:	n/a
18	chr1:144044138-144044188	ProgFib	skin:	n/a
19	chr1:144044138-144044188	AG04449	skin:	fetal
20	chr1:144044138-144044188	MCF10A-Er-Src	breast:	n/a
21	chr1:144044138-144044188	Hela-S3	cervix:	n/a
22	chr1:144044138-144044188	HCT-116	colon:	n/a
23	chr1:144044138-144044188	H1-hESC	embryonic stem cell:	embryo
24	chr1:144044138-144044188	SKMC	muscle:	n/a
25	chr1:144044138-144044188	NT2-D1	testis:	n/a
26	chr1:144044138-144044188	NHDF-neo	bronchial:	n/a
27	chr1:144044138-144044188	HPAEpiC	pulmonary alveolar:	n/a
28	chr1:144044138-144044188	GM12892	blood:	n/a
29	chr1:144044138-144044188	AoSMC	blood vessel:	n/a
30	chr1:144044138-144044188	BE2_C	brain:	n/a
31	chr1:144044138-144044188	NH-A	brain:	n/a
32	chr1:144044138-144044188	CMK	blood:	n/a
33	chr1:144044138-144044188	GM19239	blood:	n/a
34	chr1:144044138-144044188	MCF-7	breast:	n/a
35	chr1:144044138-144044188	NB4	blood:	n/a
36	chr1:144044138-144044188	SK-N-MC	brain:	n/a
37	chr1:144044138-144044188	GM12891	blood:	n/a
38	chr1:144044138-144044188	SAEC	small airway:	n/a
39	chr1:144044138-144044188	Caco-2	colon:	n/a
40	chr1:144044138-144044188	HEK293	kidney:	embryo
41	chr1:144044138-144044188	AG04450	lung:	fetal
42	chr1:144044138-144044188	HEEpiC	esophagus:	n/a
43	chr1:144044138-144044188	HIPEpiC	eye:	n/a
44	chr1:144044138-144044188	PANC-1	pancreas:	n/a
45	chr1:144044138-144044188	A549	lung:	n/a
46	chr1:144044138-144044188	HRCEpiC	kidney:	n/a
47	chr1:144044138-144044188	ECC-1	luminal epithelium:	n/a
48	chr1:144044138-144044188	HCPEpiC	choroid plexus:	n/a
49	chr1:144044138-144044188	PrEC	prostate:	n/a
50	chr1:144044138-144044188	HL-60	blood:	n/a

(count:5 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:144010495..144012548-chr1:144014486..144017526,3	MCF-7	breast:
2	chr1:144011179..144012723-chr1:144016173..144018871,2	MCF-7	breast:
3	chr1:144007296..144010001-chr1:144014414..144016453,2	K562	blood:
4	chr1:144019336..144020898-chr1:206481705..206484114,2	MCF-7	breast:
5	chr1:144005391..144007992-chr1:144016509..144019128,2	MCF-7	breast:

(count:48 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FAM72D-1	chr1:144089214-144091251	ENSG00000224363
2	lnc-FAM72D-1	chr1:144093413-144093754	NONHSAT005764
3	lnc-FAM72D-1	chr1:144093413-144093719	NONHSAT005766
4	lnc-PPIAL4B-1	chr1:144300517-144300755	NR_024584
5	lnc-FAM72D-1	chr1:144091810-144091946	ENSG00000224363
6	lnc-FAM72D-1	chr1:144088374-144088668	NONHSAT005766
7	lnc-FAM72D-1	chr1:144087901-144088049	NONHSAT005764
8	lnc-PPIAL4B-1	chr1:144300514-144300755	NONHSAT005782
9	lnc-PPIAL4B-1	chr1:144300515-144301536	ENSG00000235398
10	lnc-PPIAL4B-1	chr1:144280383-144280629	ENSG00000235398
11	lnc-PPIAL4B-1	chr1:144301350-144301536	NR_109754
12	lnc-FAM72D-1	chr1:144089058-144089129	NONHSAT005765
13	lnc-AL592284.1-3	chr1:144212643-144213017	NONHSAT005770
14	lnc-FAM72D-3	chr1:144084411-144084864	NONHSAT005763
15	lnc-FAM72D-3	chr1:144083445-144085155	ucscGeneNc_uc001eng_1
16	lnc-PPIAL4B-1	chr1:144301398-144301536	ENSG00000235398.4
17	lnc-FAM72D-1	chr1:144087482-144087804	NONHSAT005764
18	lnc-PPIAL4B-1	chr1:144300512-144301536	NONHSAT005781
19	lnc-PPIAL4B-1	chr1:144301190-144301536	NR_024584
20	lnc-AL592284.1-4	chr1:144166564-144166933	NONHSAT005769
21	lnc-PPIAL4B-1	chr1:144281066-144281169	ENSG00000235398
22	lnc-PPIAL4B-1	chr1:144280730-144280868	ENSG00000235398
23	lnc-FAM72D-1	chr1:144088374-144088668	NONHSAT005765
24	lnc-PPIAL4B-1	chr1:144301325-144301536	ENSG00000235398
25	lnc-FAM72D-1	chr1:144088423-144088668	NONHSAT005767
26	lnc-PPIAL4B-1	chr1:144301190-144301536	ENSG00000235398
27	lnc-FAM72D-1	chr1:144087901-144088049	NONHSAT005766
28	lnc-PPIAL4B-1	chr1:144326026-144326185	ENSG00000235398
29	lnc-PPIAL4B-1	chr1:144326026-144326185	ENSG00000235398
30	lnc-AL592284.1-3	chr1:144215316-144215424	NONHSAT005770
31	lnc-PPIAL4B-1	chr1:144300512-144300755	NONHSAT005780
32	lnc-FAM72D-1	chr1:144089281-144089406	NONHSAT005767
33	lnc-AL592284.1-4	chr1:144167648-144167711	NONHSAT005769
34	lnc-PPIAL4B-1	chr1:144300512-144300755	ENSG00000235398
35	lnc-FAM72D-3	chr1:144086700-144086911	NONHSAT005763
36	lnc-PPIAL4B-1	chr1:144301190-144301536	NONHSAT005780
37	lnc-AL592284.1-3	chr1:144214429-144214601	NONHSAT005770
38	lnc-FAM72D-1	chr1:144087524-144087804	NONHSAT005765
39	lnc-PPIAL4B-4	chr1:144297622-144297896	expRegAs_chr1_13930_-
40	lnc-AL592284.1-3	chr1:144213727-144213778	NONHSAT005770
41	lnc-PPIAL4B-1	chr1:144301326-144301536	ENSG00000235398.4
42	lnc-PPIAL4B-1	chr1:144325552-144325673	ENSG00000235398
43	lnc-FAM72D-1	chr1:144087684-144087804	NONHSAT005766
44	lnc-PPIAL4B-1	chr1:144325839-144326185	ENSG00000235398
45	lnc-PPIAL4B-1	chr1:144300512-144300755	NR_109754
46	lnc-PPIAL4B-1	chr1:144301190-144301536	NONHSAT005782
47	lnc-FAM72D-2	chr1:144085156-144086051	ucscGeneNc_uc001enh_1
48	lnc-PPIAL4B-1	chr1:144336229-144336254	ENSG00000235398

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location
1	NBPF15	hsa-let-7b-5p	chr1:144199965-144199985
2	NBPF15	hsa-let-7b-5p	chr1:144166620-144166640
3	NBPF15	hsa-let-7b-5p	chr1:144174551-144174571

Variant related genes	Relation type
RNVU1-4	TF binding region
ENSG00000224363	TF binding region
NBPF8	TF binding region
ENSG00000271644	TF binding region
ENSG00000231360	TF binding region
LINC00623	TF binding region
RNVU1-4	CpG island
ENSG00000224363	CpG island
NBPF8	CpG island
ENSG00000271644	CpG island
ENSG00000231360	CpG island
LINC00623	CpG island

Extended variants
information (count: 2232 )
Associated
traits (count: 178 )

Variant overlapped rSNPs/rCNVs (count:2232 , 50 per page) page: 1 2 3 4 5 6 7 ... 45

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs587601875	chr1:144015862-144015863	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs1476380	chr1:144015863-144015864	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs587715687	chr1:144015864-144015865	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs587615079	chr1:144015888-144015889	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs369936381	chr1:144015950-144015951	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs587694706	chr1:144015953-144015954	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs1476379	chr1:144015980-144015981	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs587750206	chr1:144015987-144015988	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs587652101	chr1:144015997-144015998	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs373508137	chr1:144016005-144016006	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs1476378	chr1:144016042-144016043	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs587659498	chr1:144016104-144016105	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs587743623	chr1:144016118-144016119	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs587612915	chr1:144016127-144016128	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs587702542	chr1:144016161-144016162	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs587761707	chr1:144016165-144016166	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs587634500	chr1:144016178-144016179	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs587689935	chr1:144016182-144016183	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs587753512	chr1:144016186-144016187	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs4844766	chr1:144016222-144016223	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs201612263	chr1:144016229-144016230	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs4844765	chr1:144016245-144016246	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs4844764	chr1:144016280-144016281	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs587648458	chr1:144016345-144016346	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs587676329	chr1:144016364-144016365	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs587761107	chr1:144016375-144016376	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs201161413	chr1:144016387-144016388	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs587614969	chr1:144016417-144016418	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs587671003	chr1:144016420-144016421	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs587733576	chr1:144016433-144016434	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs587629453	chr1:144016462-144016463	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs4844762	chr1:144016493-144016494	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs202228059	chr1:144016494-144016495	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs587664972	chr1:144016603-144016604	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs587738436	chr1:144016671-144016672	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs4844761	chr1:144016698-144016699	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs587604482	chr1:144016748-144016749	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs587674408	chr1:144016749-144016750	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs587736959	chr1:144016773-144016774	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs587634435	chr1:144016776-144016777	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs587695901	chr1:144016777-144016778	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs6600693	chr1:144016790-144016791	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs4844759	chr1:144016820-144016821	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
44	rs587728828	chr1:144016822-144016823	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
45	rs4844758	chr1:144016830-144016831	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
46	rs12029152	chr1:144016858-144016859	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
47	rs68158918	chr1:144016872-144016873	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
48	rs72219922	chr1:144016873-144016874	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
49	rs587618740	chr1:144016893-144016894	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
50	rs6600692	chr1:144016898-144016899	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:178)

Disease	PMID	Source
Wilms tumour	21544195	CNVD
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Cancer	21129771	CNVD
Non-small cell lung cancer	21385341	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
Ewing''s sarcoma	21437220	CNVD
Liposarcoma	21253554	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	18698080	CNVD
Melanoma	18172304	CNVD
Breast cancer	20409316	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17393978	CNVD
Cervical cancer	21062161	CNVD
Glioblastoma multiforme	21080181	CNVD
Cancer	21183584	CNVD
Multiple myeloma	16461302	CNVD
Lung cancer	18438408	CNVD
Rett syndrome	21593744	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Medulloblastoma	21979893	CNVD
Systemic lupus erythematosus	21956041	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Breast cancer	17133270	CNVD
small cell lung cancer	20016488	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Non-small cell lung cancer	21829676	CNVD
Carcinoma ex pleomorphic adenoma	18828159	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
Gastrointestinal stromal cancer	20470368	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Medulloblastoma	21292688	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	21264507	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
Neuroblastoma	21899760	CNVD
Breast cancer	17899364	CNVD
Bladder cancer	19088036	CNVD
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17002787	CNVD
Breast cancer	21858162	CNVD
Breast cancer	21611746	CNVD
Retinoblastoma	19183342	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	21990379	CNVD
Myelofibrosis	22110671	CNVD
Schizophrenia	22499536	CNVD
Schizophrenia	18923514	CNVD
Neuroblastoma	21124317	CNVD
Autism	20970697	CNVD
Bipolar disorder	19114987	CNVD
Epilepsy	20970697	CNVD
Schizophrenia	22118685	CNVD
Schizophrenia	20587603	CNVD
Schizophrenia	21285140	CNVD
Schizophrenia	20553308	CNVD
Schizophrenia	21956041	CNVD
Schizophrenia	20970697	CNVD
Addison''s disease	21851588	CNVD
Heart disease	22199024	CNVD
Mental retardation	19951919	CNVD
Ovarian cancer	20844748	CNVD
Schizophrenia	21399695	CNVD
Prostate cancer	17217626	CNVD
Congenital heart defect	22199024	CNVD
TAR Syndrome	17847015	CNVD
Thrombocytopenia-absent radius syndrome	17236129	CNVD
Autism	18784092	CNVD
Congenital abnormalities	18784092	CNVD
Mental retardation	18784092	CNVD
Schizophrenia	19855392	CNVD
Ovarian cancer	22174824	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	16608533	CNVD
Ewing''s sarcoma	22429812	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	19521722	CNVD
Mental retardation	19521722	CNVD
Schizophrenia	19521646	CNVD
Neuroblastoma	19536264	CNVD
Epilepsy	20923578	CNVD
Mental retardation	17124404	CNVD
Schizophrenia	19348701	CNVD
Schizophrenia	18668039	CNVD
Schizophrenia	19443537	CNVD
Schizophrenia	19571808	CNVD
Velocardiofacial syndrome	19329560	CNVD
Autism	19955444	CNVD
Autism	20964600	CNVD
Schizophrenia	19955444	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Colorectal cancer	20459617	CNVD
Osteosarcoma	19286668	CNVD
Osteosarcoma	17242211	CNVD
Ovarian cancer	17242211	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Schizophrenia	18990708	CNVD
Sudden cardiac death	19188705	CNVD
Plasma-cell dyscrasia	16705089	CNVD
Myeloma	17024118	CNVD
Cancer	17060936	CNVD
Multiple myeloma	16616336	CNVD
Type 2 diabetes	19141583	CNVD
Chordoma	18071362	CNVD
Hepatocellular carcinoma	18803288	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17001317	CNVD
Urothelial carcinoma	21177765	CNVD
Burkitt''s lymphoma	19759907	CNVD
Breast cancer	17142309	CNVD
Acute myeloid leukemia	21251322	CNVD
Multiple myeloma	17550852	CNVD
Prostate cancer	18632612	CNVD
Follicular lymphoma	18703704	CNVD
Lung adenocarcinoma	17982442	CNVD
Breast cancer	21509527	CNVD
Williams Syndrome	20824207	CNVD
Tetralogy of Fallot	22912587	CNVD
Autism	18522746	CNVD
early-passage human iPS cells	21368824	CNVD
Schizophrenia	23813976	CNVD
Bladder cancer	21909424	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
Acute myeloid leukemia	20729466	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Schizophrenia	19197363	CNVD
Dyslexia	22102821	CNVD
Breast cancer	22522925	CNVD
Autism	20808228	CNVD
Schizophrenia	20838587	CNVD
Schizophrenia	19805367	CNVD
Lung adenocarcinoma	21935476	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Pancreatic cancer	17952125	CNVD
Schizophrenia	20967226	CNVD
Autism	20841430	CNVD

Chromatin state (count:829 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:144006400-144019400	Strong transcription	Primary T cells from cord blood	blood
2	chr1:144009000-144017600	Weak transcription	Colonic Mucosa	Colon
3	chr1:144010400-144019000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
4	chr1:144011600-144016400	Genic enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
5	chr1:144012000-144019400	Strong transcription	Primary B cells from cord blood	blood
6	chr1:144012200-144017800	Strong transcription	Primary hematopoietic stem cells	blood
7	chr1:144012600-144020600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
8	chr1:144012800-144017000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
9	chr1:144012800-144017600	Strong transcription	Primary B cells from peripheral blood	blood
10	chr1:144013600-144016400	Genic enhancers	NHDF-Ad	bronchial
11	chr1:144013600-144016400	Genic enhancers	NHEK	skin
12	chr1:144013600-144016800	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
13	chr1:144013600-144016800	Strong transcription	HepG2	liver
14	chr1:144013600-144017000	Strong transcription	GM12878-XiMat	blood
15	chr1:144013600-144017400	Strong transcription	Primary T helper cells PMA-I stimulated	--
16	chr1:144013600-144017400	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
17	chr1:144013600-144018800	Weak transcription	Pancreatic Islets	Pancreatic Islet
18	chr1:144013800-144016000	Strong transcription	H9 Cell Line	embryonic stem cell
19	chr1:144013800-144016000	Strong transcription	Rectal Mucosa Donor 31	rectum
20	chr1:144013800-144016000	Strong transcription	Small Intestine	intestine
21	chr1:144013800-144016200	Strong transcription	iPS-18 Cell Line	embryonic stem cell
22	chr1:144013800-144016200	Genic enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
23	chr1:144013800-144016200	Genic enhancers	Aorta	Aorta
24	chr1:144013800-144016200	Genic enhancers	Brain Dorsolateral Prefrontal Cortex	brain
25	chr1:144013800-144016200	Strong transcription	Duodenum Mucosa	Duodenum
26	chr1:144013800-144016200	Strong transcription	Fetal Intestine Large	intestine
27	chr1:144013800-144016400	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
28	chr1:144013800-144016400	Genic enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
29	chr1:144013800-144016400	Strong transcription	Thymus	Thymus
30	chr1:144013800-144016600	Strong transcription	Primary T cells fromperipheralblood	blood
31	chr1:144013800-144016600	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
32	chr1:144013800-144016800	Strong transcription	H1 Cell Line	embryonic stem cell
33	chr1:144013800-144016800	Strong transcription	HUES48 Cell Line	embryonic stem cell
34	chr1:144013800-144016800	Strong transcription	Primary T killer memory cells from peripheral blood	blood
35	chr1:144013800-144016800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
36	chr1:144013800-144016800	Strong transcription	Dnd41	blood
37	chr1:144013800-144017000	Strong transcription	Fetal Thymus	thymus
38	chr1:144013800-144017200	Strong transcription	Primary hematopoietic stem cells short term culture	blood
39	chr1:144013800-144017400	Strong transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
40	chr1:144013800-144017400	Strong transcription	HUES6 Cell Line	embryonic stem cell
41	chr1:144013800-144017400	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
42	chr1:144013800-144017400	Strong transcription	Primary neutrophils fromperipheralblood	blood
43	chr1:144013800-144017400	Strong transcription	Primary T helper cells fromperipheralblood	blood
44	chr1:144013800-144017400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
45	chr1:144013800-144017600	Strong transcription	iPS-20b Cell Line	embryonic stem cell
46	chr1:144013800-144017600	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
47	chr1:144013800-144017600	Strong transcription	Spleen	Spleen
48	chr1:144013800-144017800	Strong transcription	Liver	Liver
49	chr1:144013800-144017800	Strong transcription	Stomach Smooth Muscle	stomach
50	chr1:144013800-144018200	Strong transcription	Placenta	Placenta

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