Variant report

Variant	esv2763581
Chromosome Location	chr1:92068967-92203803
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1843)
CpG islands
(count:1222)
Chromatin interactive
region (count:114)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:8)

(count:1843 , 50 per page) page: 1 2 3 4 5 6 7 ... 37

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:92072259-92072583	HepG2	liver:	n/a	n/a
2	ARID3A	chr1:92191604-92191892	HepG2	liver:	n/a	n/a
3	ARID3A	chr1:92163141-92163300	K562	blood:	n/a	n/a
4	ARID3A	chr1:92197761-92198425	K562	blood:	n/a	n/a
5	ARID3A	chr1:92190309-92190531	K562	blood:	n/a	n/a
6	ARID3A	chr1:92181905-92182533	K562	blood:	n/a	n/a
7	ARID3A	chr1:92171705-92172336	K562	blood:	n/a	n/a
8	ARID3A	chr1:92196941-92197327	K562	blood:	n/a	chr1:92197183-92197199
9	ARID3A	chr1:92202453-92203118	HepG2	liver:	n/a	n/a
10	ATF1	chr1:92181927-92182317	K562	blood:	n/a	n/a
11	ATF1	chr1:92171779-92172334	K562	blood:	n/a	n/a
12	ATF1	chr1:92178624-92179281	K562	blood:	n/a	n/a
13	ATF1	chr1:92196313-92196636	K562	blood:	n/a	n/a
14	ATF1	chr1:92197884-92198458	K562	blood:	n/a	n/a
15	ATF2	chr1:92110452-92110814	H1-hESC	embryonic stem cell:	n/a	n/a
16	ATF2	chr1:92178671-92179395	GM12878	blood:	n/a	n/a
17	ATF3	chr1:92196237-92196599	K562	blood:	n/a	n/a
18	ATF3	chr1:92197931-92198501	K562	blood:	n/a	n/a
19	ATF3	chr1:92198028-92198372	K562	blood:	n/a	n/a
20	BACH1	chr1:92197491-92198200	K562	blood:	n/a	n/a
21	BACH1	chr1:92069256-92069294	K562	blood:	n/a	n/a
22	BACH1	chr1:92179079-92179250	H1-hESC	embryonic stem cell:	n/a	n/a
23	BACH1	chr1:92172316-92172596	K562	blood:	n/a	n/a
24	BACH1	chr1:92183826-92183910	K562	blood:	n/a	n/a
25	BATF	chr1:92162962-92163345	GM12878	blood:	n/a	n/a
26	BATF	chr1:92068907-92069264	GM12878	blood:	n/a	n/a
27	BATF	chr1:92178946-92179304	GM12878	blood:	n/a	n/a
28	BATF	chr1:92162955-92163389	GM12878	blood:	n/a	n/a
29	BCL3	chr1:92197385-92197844	A549	lung:	n/a	chr1:92197586-92197595
30	BCL3	chr1:92197333-92197701	GM12878	blood:	n/a	chr1:92197586-92197595
31	BCL3	chr1:92197434-92197789	A549	lung:	n/a	chr1:92197586-92197595
32	BCLAF1	chr1:92178690-92179438	GM12878	blood:	n/a	chr1:92179162-92179171 chr1:92179161-92179170
33	BCLAF1	chr1:92175696-92176195	GM12878	blood:	n/a	n/a
34	BHLHE40	chr1:92117159-92117406	K562	blood:	n/a	n/a
35	BHLHE40	chr1:92191192-92191235	K562	blood:	n/a	n/a
36	BHLHE40	chr1:92178632-92179229	K562	blood:	n/a	n/a
37	BHLHE40	chr1:92180324-92181000	K562	blood:	n/a	n/a
38	BHLHE40	chr1:92195148-92195280	K562	blood:	n/a	n/a
39	BHLHE40	chr1:92171698-92172130	K562	blood:	n/a	n/a
40	BHLHE40	chr1:92202481-92202959	HepG2	liver:	n/a	n/a
41	BHLHE40	chr1:92181837-92182347	K562	blood:	n/a	n/a
42	BHLHE40	chr1:92202555-92202860	A549	lung:	n/a	n/a
43	BHLHE40	chr1:92196306-92198601	K562	blood:	n/a	n/a
44	BHLHE40	chr1:92179668-92179800	GM12878	blood:	n/a	chr1:92179708-92179721
45	BRCA1	chr1:92202431-92202939	Hela-S3	cervix:	n/a	n/a
46	BRCA1	chr1:92200064-92200100	GM12878	blood:	n/a	n/a
47	BRCA1	chr1:92083235-92083374	Hela-S3	cervix:	n/a	n/a
48	BRCA1	chr1:92079175-92079817	Hela-S3	cervix:	n/a	n/a
49	BRCA1	chr1:92076916-92077359	Hela-S3	cervix:	n/a	n/a
50	CBX3	chr1:92121412-92122078	K562	blood:	n/a	n/a

(count:1222 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:92191625-92191675	NH-A	brain:	n/a
2	chr1:92154087-92154137	HMEC	breast:	n/a
3	chr1:92191625-92191675	NH-A	brain:	n/a
4	chr1:92154087-92154137	HMEC	breast:	n/a
5	chr1:92102055-92102105	HPAEpiC	pulmonary alveolar:	n/a
6	chr1:92179761-92179811	HUVEC	blood vessel:	n/a
7	chr1:92100082-92100132	BJ	skin:	n/a
8	chr1:92154087-92154137	SK-N-SH_RA	brain:	n/a
9	chr1:92179761-92179811	GM12891	blood:	n/a
10	chr1:92171309-92171359	HCF	heart:	n/a
11	chr1:92101219-92101269	HNPCEpiC	eye:	n/a
12	chr1:92149139-92149189	HNPCEpiC	eye:	n/a
13	chr1:92149139-92149189	HAEpiC	amniotic membrane:	n/a
14	chr1:92099858-92099908	SAEC	small airway:	n/a
15	chr1:92203667-92203717	AG09319	gingival:	n/a
16	chr1:92197531-92197581	PANC-1	pancreas:	n/a
17	chr1:92149139-92149189	HCT-116	colon:	n/a
18	chr1:92203667-92203717	HRCEpiC	kidney:	n/a
19	chr1:92110813-92110863	PFSK-1	brain:	n/a
20	chr1:92135648-92135698	SAEC	small airway:	n/a
21	chr1:92171309-92171359	Caco-2	colon:	n/a
22	chr1:92191625-92191675	AoSMC	blood vessel:	n/a
23	chr1:92102055-92102105	NT2-D1	testis:	n/a
24	chr1:92083173-92083223	GM19239	blood:	n/a
25	chr1:92154087-92154137	HCT-116	colon:	n/a
26	chr1:92154087-92154137	HPAEpiC	pulmonary alveolar:	n/a
27	chr1:92099858-92099908	HMEC	breast:	n/a
28	chr1:92135648-92135698	Hela-S3	cervix:	n/a
29	chr1:92099528-92099578	PANC-1	pancreas:	n/a
30	chr1:92099528-92099578	Hepatocyte	liver:	n/a
31	chr1:92099528-92099578	PFSK-1	brain:	n/a
32	chr1:92110813-92110863	NB4	blood:	n/a
33	chr1:92135648-92135698	HCPEpiC	choroid plexus:	n/a
34	chr1:92171309-92171359	HEEpiC	esophagus:	n/a
35	chr1:92102055-92102105	NB4	blood:	n/a
36	chr1:92171309-92171359	HAEpiC	amniotic membrane:	n/a
37	chr1:92135648-92135698	PANC-1	pancreas:	n/a
38	chr1:92083173-92083223	NT2-D1	testis:	n/a
39	chr1:92100082-92100132	AG10803	skin:	n/a
40	chr1:92110813-92110863	HAEpiC	amniotic membrane:	n/a
41	chr1:92099858-92099908	A549	lung:	n/a
42	chr1:92149139-92149189	HRCEpiC	kidney:	n/a
43	chr1:92191625-92191675	NHDF-neo	bronchial:	n/a
44	chr1:92117004-92117054	Hepatocyte	liver:	n/a
45	chr1:92135648-92135698	HEK293	kidney:	embryo
46	chr1:92154087-92154137	HIPEpiC	eye:	n/a
47	chr1:92117004-92117054	SKMC	muscle:	n/a
48	chr1:92075595-92075645	GM06990	blood:	n/a
49	chr1:92101219-92101269	MCF10A-Er-Src	breast:	n/a
50	chr1:92099858-92099908	PANC-1	pancreas:	n/a

(count:114 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr1:92189655..92191426-chr1:92192587..92194510,2	K562	blood:
2	chr1:92151670..92153207-chr1:92161456..92163644,2	K562	blood:
3	chr1:92081027..92084138-chr1:92090096..92093775,3	K562	blood:
4	chr1:92171556..92174319-chr1:92192044..92194001,2	K562	blood:
5	chr1:92121261..92123994-chr1:92125259..92127576,2	K562	blood:
6	chr1:92180489..92182487-chr1:92191711..92193965,2	K562	blood:
7	chr1:92094905..92097332-chr1:92098172..92099750,2	K562	blood:
8	chr1:92114681..92117340-chr1:92119147..92120914,2	K562	blood:
9	chr1:92143583..92146461-chr1:92147900..92150725,3	K562	blood:
10	chr1:92177009..92179682-chr1:92195748..92197642,2	K562	blood:
11	chr1:92182554..92184890-chr1:92189322..92192184,2	K562	blood:
12	chr1:92082816..92083446-chr1:92348571..92349551,5	MCF-7	breast:
13	chr1:92111029..92113050-chr1:92113299..92116260,2	K562	blood:
14	chr1:92067249..92070219-chr1:92074709..92076906,3	K562	blood:
15	chr1:92162419..92166265-chr1:92170255..92173059,5	K562	blood:
16	chr1:92093633..92096261-chr1:92193421..92196106,2	K562	blood:
17	chr1:92111551..92113673-chr1:92116483..92118232,2	K562	blood:
18	chr1:92196960..92199922-chr1:92201744..92205146,4	K562	blood:
19	chr1:92196718..92198594-chr1:92235219..92237131,2	K562	blood:
20	chr1:92067249..92070219-chr1:92074709..92076665,2	K562	blood:
21	chr1:92196960..92199922-chr1:92201744..92205146,4	K562	blood:
22	chr1:92194536..92198402-chr1:92243329..92245903,3	K562	blood:
23	chr1:92155914..92157539-chr1:92165115..92168054,2	K562	blood:
24	chr1:92181357..92183863-chr1:92196120..92197770,2	K562	blood:
25	chr1:92196725..92200248-chr1:92206849..92210560,4	K562	blood:
26	chr1:92162441..92164446-chr1:92195933..92198118,2	K562	blood:
27	chr1:92154030..92157001-chr1:92158555..92160542,2	K562	blood:
28	chr1:92197202..92203288-chr1:92206365..92210533,5	K562	blood:
29	chr1:92100975..92102811-chr1:92111120..92112791,2	K562	blood:
30	chr1:92160729..92163460-chr1:92181543..92183054,2	K562	blood:
31	chr1:92178299..92180371-chr1:92198181..92200886,2	K562	blood:
32	chr1:92166312..92168639-chr1:92169592..92172203,2	K562	blood:
33	chr1:92161234..92163653-chr1:92164578..92167182,3	K562	blood:
34	chr1:92162441..92164446-chr1:92195933..92198118,2	K562	blood:
35	chr1:92189258..92193188-chr1:92194522..92196591,3	K562	blood:
36	chr1:92160729..92163460-chr1:92181543..92183054,2	K562	blood:
37	chr1:92143583..92146461-chr1:92147900..92150725,3	K562	blood:
38	chr1:92097267..92098889-chr1:92337688..92339607,2	K562	blood:
39	chr1:92067249..92070219-chr1:92074709..92076906,3	K562	blood:
40	chr1:92059728..92061441-chr1:92068842..92071690,2	K562	blood:
41	chr1:92162419..92165412-chr1:92170320..92173271,4	K562	blood:
42	chr1:92171820..92173594-chr1:92174594..92176348,2	K562	blood:
43	chr1:92170602..92173339-chr1:92193646..92196655,3	K562	blood:
44	chr1:92085074..92086910-chr1:92278209..92279900,2	K562	blood:
45	chr1:92171317..92173686-chr1:92182060..92185039,2	K562	blood:
46	chr1:92116629..92119391-chr1:92121529..92123186,2	K562	blood:
47	chr1:92198271..92200616-chr1:92212506..92214595,2	MCF-7	breast:
48	chr1:92198152..92200213-chr1:92201193..92206399,7	K562	blood:
49	chr1:92189258..92193188-chr1:92194522..92196591,3	K562	blood:
50	chr1:92100975..92102811-chr1:92111120..92112791,2	K562	blood:

No data

(count:8 , 50 per page) page: 1

No.	miRNA target gene	miRNA name	Chromosome Location
1	TGFBR3	hsa-miR-101-3p	chr1:92146310-92146303
2	TGFBR3	hsa-miR-21-5p	chr1:92147733-92147755
3	TGFBR3	hsa-miR-101-3p	chr1:92146304-92146323
4	TGFBR3	hsa-miR-101-3p	chr1:92147198-92147219
5	TGFBR3	hsa-miR-193b-3p	chr1:92146036-92146057
6	TGFBR3	hsa-miR-181a-5p	chr1:92147377-92147371
7	TGFBR3	hsa-miR-21-5p	chr1:92148000-92148022
8	TGFBR3	hsa-miR-193b-3p	chr1:92146042-92146036

Variant related genes	Relation type
HSP90B3P	TF binding region
TGFBR3	TF binding region
HSP90B3P	CpG island
TGFBR3	CpG island
ENSG00000069702	chromatin interactions

Extended variants
information (count: 5253 )
Associated
traits (count: 102 )

Variant overlapped rSNPs/rCNVs (count:5253 , 50 per page) page: 1 2 3 4 5 6 7 ... 106

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1192404	chr1:92068967-92068968	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs529629071	chr1:92069041-92069042	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs193111263	chr1:92069071-92069072	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs185514008	chr1:92069079-92069080	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs530066579	chr1:92069113-92069114	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs374424672	chr1:92069114-92069115	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs532612409	chr1:92069133-92069134	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs189362333	chr1:92069135-92069136	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs80309284	chr1:92069153-92069154	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs12564910	chr1:92069157-92069158	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs1192405	chr1:92069172-92069173	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs4658244	chr1:92069188-92069189	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs552202072	chr1:92069250-92069251	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs537764166	chr1:92069271-92069272	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs565851639	chr1:92069293-92069294	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs558843215	chr1:92069343-92069344	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs138851200	chr1:92069401-92069402	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs534410690	chr1:92069461-92069462	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs1192406	chr1:92069466-92069467	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs574080008	chr1:92069477-92069478	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs535133977	chr1:92069519-92069520	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs74535710	chr1:92069533-92069534	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs117144645	chr1:92069637-92069638	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs12724439	chr1:92069663-92069664	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs1192407	chr1:92069689-92069690	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs192692012	chr1:92069718-92069719	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs184115518	chr1:92069731-92069732	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs559912003	chr1:92069756-92069757	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs375954736	chr1:92069821-92069822	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs567721064	chr1:92069853-92069854	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs188464859	chr1:92069874-92069875	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs1192408	chr1:92069892-92069893	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs369018881	chr1:92069906-92069907	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs531065174	chr1:92069923-92069924	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs376991484	chr1:92069932-92069933	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs1192409	chr1:92069939-92069940	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs570702924	chr1:92069948-92069949	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs1192410	chr1:92069964-92069965	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs539306121	chr1:92069976-92069977	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs181090519	chr1:92069980-92069981	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs567790781	chr1:92070047-92070048	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs12031900	chr1:92070093-92070094	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs55882031	chr1:92070141-92070142	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs575200189	chr1:92070186-92070187	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs552412608	chr1:92070207-92070208	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs185923544	chr1:92070227-92070228	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs116155597	chr1:92070258-92070259	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs541301130	chr1:92070262-92070263	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs373522794	chr1:92070280-92070281	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs144790464	chr1:92070328-92070329	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:102)

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
Breast cancer	22522925	CNVD
Lung adenocarcinoma	21935476	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
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:2808 , 50 per page) page: 1 2 3 4 5 6 7 ... 57

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:92055800-92076400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr1:92057200-92070400	Weak transcription	Psoas Muscle	Psoas
3	chr1:92060600-92070200	Weak transcription	Right Ventricle	heart
4	chr1:92060800-92070200	Weak transcription	Rectal Smooth Muscle	rectum
5	chr1:92061200-92070000	Weak transcription	Ovary	ovary
6	chr1:92062400-92074200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
7	chr1:92064000-92070000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
8	chr1:92066000-92069200	Enhancers	NHDF-Ad	bronchial
9	chr1:92066400-92069000	Weak transcription	Fetal Kidney	kidney
10	chr1:92066800-92069000	Weak transcription	Right Atrium	heart
11	chr1:92067600-92071600	Weak transcription	Spleen	Spleen
12	chr1:92067800-92070000	Weak transcription	Stomach Smooth Muscle	stomach
13	chr1:92067800-92070400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
14	chr1:92068000-92069000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
15	chr1:92068200-92070000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
16	chr1:92068200-92070000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
17	chr1:92068200-92070000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
18	chr1:92068200-92070000	Weak transcription	Fetal Stomach	stomach
19	chr1:92068200-92070000	Weak transcription	Left Ventricle	heart
20	chr1:92068200-92071800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
21	chr1:92068200-92083800	Weak transcription	Fetal Lung	lung
22	chr1:92068400-92069400	Weak transcription	Fetal Heart	heart
23	chr1:92068400-92070200	Weak transcription	Adipose Nuclei	Adipose
24	chr1:92068600-92070000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
25	chr1:92068600-92070000	Weak transcription	Fetal Muscle Trunk	muscle
26	chr1:92068800-92069600	Enhancers	GM12878-XiMat	blood
27	chr1:92068800-92070000	Weak transcription	Fetal Muscle Leg	muscle
28	chr1:92068800-92074400	Weak transcription	Placenta	Placenta
29	chr1:92069000-92069200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
30	chr1:92069000-92069200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
31	chr1:92069000-92069600	Enhancers	Fetal Kidney	kidney
32	chr1:92069000-92069600	Enhancers	Right Atrium	heart
33	chr1:92069200-92070000	Weak transcription	NHDF-Ad	bronchial
34	chr1:92069200-92072000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
35	chr1:92069400-92072800	Enhancers	Fetal Heart	heart
36	chr1:92069600-92070000	Weak transcription	Right Atrium	heart
37	chr1:92069600-92074400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
38	chr1:92070000-92070200	Enhancers	Right Atrium	heart
39	chr1:92070000-92070200	Enhancers	Stomach Smooth Muscle	stomach
40	chr1:92070000-92070600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
41	chr1:92070000-92070600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
42	chr1:92070000-92070600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
43	chr1:92070000-92070600	Enhancers	Left Ventricle	heart
44	chr1:92070000-92070600	Enhancers	Hela-S3	cervix
45	chr1:92070000-92070800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
46	chr1:92070000-92070800	Enhancers	Muscle Satellite Cultured Cells	--
47	chr1:92070000-92070800	Enhancers	Ovary	ovary
48	chr1:92070000-92070800	Enhancers	HSMM	muscle
49	chr1:92070000-92070800	Enhancers	HSMMtube	muscle
50	chr1:92070000-92070800	Enhancers	NHDF-Ad	bronchial

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