Variant report

Variant	nsv819786
Chromosome Location	chr1:114444112-114446238
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:32)
CpG islands
(count:61)
Chromatin interactive
region (count:14)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:32 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CEBPB	chr1:114446129-114448738	MCF-7	breast:	n/a	n/a
2	CHD2	chr1:114446197-114446229	GM12878	blood:	n/a	n/a
3	E2F4	chr1:114445281-114445431	MCF10A-Er-Src	breast:	n/a	n/a
4	EBF1	chr1:114446221-114446975	GM12878	blood:	n/a	chr1:114446540-114446551
5	ELF1	chr1:114446225-114448742	MCF-7	breast:	n/a	n/a
6	EP300	chr1:114446179-114446465	GM12878	blood:	n/a	n/a
7	FOS	chr1:114445485-114445575	MCF10A-Er-Src	breast:	n/a	n/a
8	GABPA	chr1:114446004-114448722	MCF-7	breast:	n/a	n/a
9	HDAC2	chr1:114445980-114448756	MCF-7	breast:	n/a	n/a
10	JUN	chr1:114445974-114448749	K562	blood:	n/a	chr1:114446687-114446701
11	MAX	chr1:114445917-114448671	MCF-7	breast:	n/a	chr1:114448611-114448620 chr1:114447122-114447131
12	MAX	chr1:114446149-114448674	MCF-7	breast:	n/a	chr1:114448611-114448620 chr1:114447122-114447131
13	MAZ	chr1:114446193-114448140	GM12878	blood:	n/a	chr1:114447122-114447131
14	MXI1	chr1:114446101-114446301	GM12878	blood:	n/a	n/a
15	MXI1	chr1:114446060-114448767	SK-N-SH	brain:	n/a	n/a
16	NR2F2	chr1:114446024-114448746	MCF-7	breast:	n/a	n/a
17	PML	chr1:114446225-114448700	MCF-7	breast:	n/a	n/a
18	PML	chr1:114446232-114448498	GM12878	blood:	n/a	n/a
19	POLR2A	chr1:114446088-114448562	GM12891	blood:	n/a	n/a
20	POLR2A	chr1:114446026-114448464	GM12878	blood:	n/a	n/a
21	POLR2A	chr1:114446190-114448381	GM18505	blood:	n/a	n/a
22	RCOR1	chr1:114446180-114448135	GM12878	blood:	n/a	n/a
23	RELA	chr1:114446179-114448245	GM15510	blood:	n/a	n/a
24	SIN3AK20	chr1:114445935-114448789	MCF-7	breast:	n/a	n/a
25	SIN3AK20	chr1:114445852-114449210	MCF-7	breast:	n/a	n/a
26	SMC3	chr1:114446196-114446495	GM12878	blood:	n/a	n/a
27	SPI1	chr1:114446050-114446381	GM12891	blood:	n/a	n/a
28	SPI1	chr1:114446054-114446360	GM12878	blood:	n/a	n/a
29	SPI1	chr1:114445968-114446511	HL-60	blood:	n/a	n/a
30	STAT3	chr1:114446187-114446501	GM12878	blood:	n/a	n/a
31	TBP	chr1:114446235-114448108	GM12878	blood:	n/a	n/a
32	WRNIP1	chr1:114445368-114445549	GM12878	blood:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:114444754-114444804	AG10803	skin:	n/a
2	chr1:114444754-114444804	MCF-7	breast:	n/a
3	chr1:114444754-114444804	PANC-1	pancreas:	n/a
4	chr1:114444754-114444804	PFSK-1	brain:	n/a
5	chr1:114444754-114444804	AG09319	gingival:	n/a
6	chr1:114444754-114444804	AG04449	skin:	fetal
7	chr1:114444754-114444804	HUVEC	blood vessel:	n/a
8	chr1:114444754-114444804	HRCEpiC	kidney:	n/a
9	chr1:114444754-114444804	SK-N-SH_RA	brain:	n/a
10	chr1:114444754-114444804	SKMC	muscle:	n/a
11	chr1:114444754-114444804	NB4	blood:	n/a
12	chr1:114444754-114444804	CMK	blood:	n/a
13	chr1:114444754-114444804	GM12891	blood:	n/a
14	chr1:114444754-114444804	HepG2	liver:	n/a
15	chr1:114444754-114444804	HNPCEpiC	eye:	n/a
16	chr1:114444754-114444804	BJ	skin:	n/a
17	chr1:114444754-114444804	HL-60	blood:	n/a
18	chr1:114444754-114444804	ProgFib	skin:	n/a
19	chr1:114444754-114444804	AoSMC	blood vessel:	n/a
20	chr1:114444754-114444804	GM12878	blood:	n/a
21	chr1:114444754-114444804	H1-hESC	embryonic stem cell:	embryo
22	chr1:114444754-114444804	MCF10A-Er-Src	breast:	n/a
23	chr1:114444754-114444804	T-47D	breast:	n/a
24	chr1:114444754-114444804	AG04450	lung:	fetal
25	chr1:114444754-114444804	SK-N-MC	brain:	n/a
26	chr1:114444754-114444804	ovcar-3	ovarian:	n/a
27	chr1:114444754-114444804	GM12892	blood:	n/a
28	chr1:114444754-114444804	NHBE	bronchial:	n/a
29	chr1:114444754-114444804	SAEC	small airway:	n/a
30	chr1:114444754-114444804	SK-N-SH	brain:	n/a
31	chr1:114444754-114444804	HPAEpiC	pulmonary alveolar:	n/a
32	chr1:114444754-114444804	AG09309	skin:	n/a
33	chr1:114444754-114444804	HCF	heart:	n/a
34	chr1:114444754-114444804	RPTEC	kidney:	n/a
35	chr1:114444754-114444804	HAEpiC	amniotic membrane:	n/a
36	chr1:114444754-114444804	ECC-1	luminal epithelium:	n/a
37	chr1:114444754-114444804	LNCaP	prostate:	n/a
38	chr1:114444754-114444804	BE2_C	brain:	n/a
39	chr1:114444754-114444804	IMR90	lung:	fetal
40	chr1:114444754-114444804	A549	lung:	n/a
41	chr1:114444754-114444804	HRPEpiC	eye:	n/a
42	chr1:114444754-114444804	HCT-116	colon:	n/a
43	chr1:114444754-114444804	NH-A	brain:	n/a
44	chr1:114444754-114444804	HCM	heart:	n/a
45	chr1:114444754-114444804	HEK293	kidney:	embryo
46	chr1:114444754-114444804	Hepatocyte	liver:	n/a
47	chr1:114444754-114444804	HRE	kidney:	n/a
48	chr1:114444754-114444804	PrEC	prostate:	n/a
49	chr1:114444754-114444804	K562	blood:	n/a
50	chr1:114444754-114444804	HCPEpiC	choroid plexus:	n/a

(count:14 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:114353620..114357151-chr1:114445438..114449458,6	K562	blood:
2	chr1:114361850..114364464-chr1:114444259..114447022,2	MCF-7	breast:
3	chr1:114445771..114447458-chr9:132251917..132254040,2	MCF-7	breast:
4	chr1:114299428..114302166-chr1:114446012..114448303,2	K562	blood:
5	chr1:114300712..114302958-chr1:114446093..114449659,3	MCF-7	breast:
6	chr1:114446144..114448333-chr19:16187175..16189942,2	MCF-7	breast:
7	chr1:114445068..114448942-chr1:115050232..115055017,4	MCF-7	breast:
8	chr1:114446008..114448199-chr1:114495493..114497584,2	MCF-7	breast:
9	chr1:114300422..114303875-chr1:114445198..114448512,7	MCF-7	breast:
10	chr1:114446165..114448738-chr1:115053730..115055909,2	MCF-7	breast:
11	chr1:114444168..114452207-chr1:114466193..114476714,61	K562	blood:
12	chr1:114352306..114358140-chr1:114445806..114450844,18	MCF-7	breast:
13	chr1:114352137..114357235-chr1:114445065..114452395,18	MCF-7	breast:
14	chr1:114445859..114448805-chr17:42295421..42298283,3	MCF-7	breast:

No data

Variant related genes	Relation type
DCLRE1B	TF binding region
AP4B1	TF binding region
DCLRE1B	CpG island
AP4B1	CpG island
ENSG00000204054	chromatin interactions
ENSG00000167460	chromatin interactions
ENSG00000235527	chromatin interactions
ENSG00000197323	chromatin interactions
ENSG00000116793	chromatin interactions
ENSG00000163349	chromatin interactions
ENSG00000081019	chromatin interactions
ENSG00000134242	chromatin interactions
ENSG00000231128	chromatin interactions
ENSG00000108312	chromatin interactions

Extended variants
information (count: 99 )
Associated
traits (count: 101 )

Variant overlapped rSNPs/rCNVs (count:99 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs79534272	chr1:114444144-114444145	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs77831247	chr1:114444154-114444155	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs554274805	chr1:114444184-114444185	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs557191782	chr1:114444200-114444201	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs143683107	chr1:114444299-114444300	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs542693038	chr1:114444302-114444303	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs559212401	chr1:114444314-114444315	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs78563784	chr1:114444322-114444323	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs185948622	chr1:114444328-114444329	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs368146491	chr1:114444339-114444340	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs549396865	chr1:114444348-114444349	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs34751342	chr1:114444444-114444445	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs147043117	chr1:114444457-114444458	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs550100552	chr1:114444458-114444459	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs143769705	chr1:114444473-114444474	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs371683713	chr1:114444477-114444478	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs75117963	chr1:114444484-114444485	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs138880168	chr1:114444488-114444489	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs375975068	chr1:114444496-114444497	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs529490243	chr1:114444522-114444523	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs549574613	chr1:114444547-114444548	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs573648846	chr1:114444574-114444575	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs12079716	chr1:114444594-114444595	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Active TSS	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	disease
24	rs377159938	chr1:114444598-114444599	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs551755388	chr1:114444615-114444616	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs369892580	chr1:114444640-114444641	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs74706689	chr1:114444656-114444657	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs189259390	chr1:114444682-114444683	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs557328961	chr1:114444724-114444725	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs573758056	chr1:114444754-114444755	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Active TSS	CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
31	rs536032288	chr1:114444761-114444762	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Active TSS	CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
32	rs553149311	chr1:114444770-114444771	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Active TSS	CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
33	rs112059103	chr1:114444773-114444774	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Active TSS	CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
34	rs544750052	chr1:114444840-114444841	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs564528571	chr1:114444867-114444868	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs574928114	chr1:114444895-114444896	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs543685230	chr1:114444909-114444910	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs112921678	chr1:114444914-114444915	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs374609197	chr1:114444948-114444949	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs77493246	chr1:114444975-114444976	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs376516195	chr1:114444997-114444998	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs563798493	chr1:114445004-114445005	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs529603033	chr1:114445030-114445031	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs549267856	chr1:114445056-114445057	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs182216995	chr1:114445098-114445099	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Active TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
46	rs528594952	chr1:114445119-114445120	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Active TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
47	rs551948046	chr1:114445145-114445146	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Active TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
48	rs187229500	chr1:114445201-114445202	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
49	rs368872641	chr1:114445236-114445237	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
50	rs537405509	chr1:114445237-114445238	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:101)

Disease	PMID	Source
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
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
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17393978	CNVD
Medulloblastoma	21979893	CNVD
Cervical cancer	21062161	CNVD
Cancer	21183584	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21364760	CNVD
Rett syndrome	21593744	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ovarian cancer	21720365	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Pancreatic endocrine tumor	17639061	CNVD
small cell lung cancer	20016488	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Multiple myeloma	17550852	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Asthma	20841430	CNVD
Aetanephric adenomas	20802469	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Multiple myeloma	16616336	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Systemic lupus erythematosus	21956041	CNVD
Cancer	20164920	CNVD
Myelofibrosis	22110671	CNVD
Gastric adenocarcinoma	19115996	CNVD
Ovarian neoplasms	16753589	CNVD
Prostate cancer	16573809	CNVD
Glioma	17123091	CNVD
Lung cancer	16773561	CNVD
Breast cancer	17899364	CNVD
Cutaneous malignant melanoma	17690212	CNVD
Melanoma	19671679	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Bipolar disorder	19114987	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:324 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:114415000-114447000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
2	chr1:114420200-114446400	Weak transcription	Aorta	Aorta
3	chr1:114431800-114445400	Weak transcription	Stomach Mucosa	stomach
4	chr1:114434800-114446200	Weak transcription	Fetal Heart	heart
5	chr1:114435600-114446200	Weak transcription	H1 Cell Line	embryonic stem cell
6	chr1:114435600-114446400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
7	chr1:114435800-114444400	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
8	chr1:114436000-114444600	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
9	chr1:114436000-114446800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
10	chr1:114436200-114444600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
11	chr1:114436200-114444600	Strong transcription	Stomach Smooth Muscle	stomach
12	chr1:114436200-114445200	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
13	chr1:114436200-114446600	Weak transcription	H9 Cell Line	embryonic stem cell
14	chr1:114436200-114446600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
15	chr1:114436400-114444200	Strong transcription	Primary T cells fromperipheralblood	blood
16	chr1:114436400-114444600	Strong transcription	Primary T cells from cord blood	blood
17	chr1:114436400-114445000	Strong transcription	Liver	Liver
18	chr1:114436400-114445200	Strong transcription	Brain Anterior Caudate	brain
19	chr1:114436400-114445600	Strong transcription	Breast Myoepithelial Primary Cells	Breast
20	chr1:114436600-114444600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
21	chr1:114436600-114445600	Strong transcription	Fetal Thymus	thymus
22	chr1:114436800-114444400	Strong transcription	Dnd41	blood
23	chr1:114436800-114445200	Strong transcription	Skeletal Muscle Female	skeletal muscle
24	chr1:114436800-114445600	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
25	chr1:114436800-114445600	Strong transcription	Osteobl	bone
26	chr1:114436800-114446400	Strong transcription	Fetal Muscle Trunk	muscle
27	chr1:114437000-114444600	Strong transcription	Thymus	Thymus
28	chr1:114437000-114445600	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
29	chr1:114437000-114445600	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
30	chr1:114437000-114445600	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
31	chr1:114437200-114444400	Strong transcription	Sigmoid Colon	Sigmoid Colon
32	chr1:114437200-114444600	Strong transcription	HUES64 Cell Line	embryonic stem cell
33	chr1:114437200-114445600	Strong transcription	Fetal Muscle Leg	muscle
34	chr1:114437400-114444200	Strong transcription	Skeletal Muscle Male	skeletal muscle
35	chr1:114437400-114444400	Strong transcription	Placenta	Placenta
36	chr1:114437400-114445200	Strong transcription	Primary hematopoietic stem cells short term culture	blood
37	chr1:114437400-114445400	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
38	chr1:114437400-114445600	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
39	chr1:114437600-114444600	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
40	chr1:114437600-114446400	Weak transcription	Pancreatic Islets	Pancreatic Islet
41	chr1:114437800-114444400	Strong transcription	Cortex derived primary cultured neurospheres	brain
42	chr1:114437800-114445400	Strong transcription	Brain Germinal Matrix	brain
43	chr1:114437800-114445400	Strong transcription	Brain Hippocampus Middle	brain
44	chr1:114437800-114445400	Strong transcription	Left Ventricle	heart
45	chr1:114438800-114445200	Strong transcription	Brain Dorsolateral Prefrontal Cortex	brain
46	chr1:114439200-114446400	Weak transcription	Placenta Amnion	Placenta Amnion
47	chr1:114439400-114444400	Strong transcription	NH-A	brain
48	chr1:114440200-114445200	Strong transcription	K562	blood
49	chr1:114440200-114445400	Strong transcription	Primary hematopoietic stem cells	blood
50	chr1:114440400-114444600	Strong transcription	NHLF	lung

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