Variant report

Variant	nsv437503
Chromosome Location	chr6:33408542-33421577
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:239)
CpG islands
(count:1956)
Chromatin interactive
region (count:24)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:1)

(count:239 , 50 per page) page: 1 2 3 4 5

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BHLHE40	chr6:33408403-33408663	K562	blood:	n/a	n/a
2	CBX3	chr6:33421427-33422762	K562	blood:	n/a	chr6:33421765-33421776
3	CBX3	chr6:33408360-33408776	K562	blood:	n/a	n/a
4	CCNT2	chr6:33408504-33408719	K562	blood:	n/a	n/a
5	CEBPB	chr6:33415467-33415524	HepG2	liver:	n/a	chr6:33415482-33415493
6	CREB1	chr6:33421434-33422769	HepG2	liver:	n/a	n/a
7	CTCF	chr6:33419499-33419554	GM13976	blood:	n/a	n/a
8	CTCF	chr6:33415880-33416030	HepG2	liver:	n/a	n/a
9	CTCF	chr6:33415740-33415890	HEK293	kidney:	n/a	n/a
10	CTCF	chr6:33415780-33415930	WERI-Rb-1	eye:	n/a	n/a
11	E2F6	chr6:33408437-33408675	K562	blood:	n/a	n/a
12	ELF1	chr6:33408417-33408738	K562	blood:	n/a	n/a
13	ELF1	chr6:33408358-33408745	K562	blood:	n/a	n/a
14	EP300	chr6:33408471-33408713	K562	blood:	n/a	n/a
15	GABPA	chr6:33421478-33423029	MCF-7	breast:	n/a	chr6:33422309-33422318
16	GATA1	chr6:33421344-33422659	PBDE	blood:	n/a	chr6:33421824-33421835 chr6:33421720-33421732 chr6:33422578-33422599 chr6:33421829-33421839 chr6:33422585-33422592 chr6:33421726-33421733 chr6:33422585-33422592 chr6:33422585-33422592 chr6:33422584-33422594
17	HCFC1	chr6:33421311-33423096	Hela-S3	cervix:	n/a	n/a
18	HMGN3	chr6:33410911-33411108	K562	blood:	n/a	n/a
19	HMGN3	chr6:33408401-33408676	K562	blood:	n/a	n/a
20	IRF1	chr6:33421450-33422738	K562	blood:	n/a	chr6:33422253-33422262 chr6:33422290-33422299 chr6:33422228-33422242
21	JUN	chr6:33421247-33422990	K562	blood:	n/a	n/a
22	JUN	chr6:33408347-33408618	K562	blood:	n/a	n/a
23	JUN	chr6:33407549-33409035	K562	blood:	n/a	n/a
24	JUND	chr6:33413822-33413867	H1-hESC	embryonic stem cell:	n/a	n/a
25	JUND	chr6:33408398-33408778	K562	blood:	n/a	n/a
26	MAFF	chr6:33418873-33419157	HepG2	liver:	n/a	n/a
27	MAFK	chr6:33418860-33419122	HepG2	liver:	n/a	n/a
28	MAFK	chr6:33418959-33419064	Hela-S3	cervix:	n/a	n/a
29	MAX	chr6:33413215-33413400	NB4	blood:	n/a	n/a
30	MAX	chr6:33408400-33408750	K562	blood:	n/a	n/a
31	MAX	chr6:33407648-33408693	K562	blood:	n/a	n/a
32	MAX	chr6:33408410-33408636	K562	blood:	n/a	n/a
33	MAZ	chr6:33407791-33408825	K562	blood:	n/a	n/a
34	MAZ	chr6:33421350-33421510	K562	blood:	n/a	n/a
35	MXI1	chr6:33421333-33423155	IMR90	lung:	n/a	n/a
36	MXI1	chr6:33421139-33423543	SK-N-SH	brain:	n/a	n/a
37	MYC	chr6:33421537-33422618	NB4	blood:	n/a	n/a
38	MYC	chr6:33421507-33422811	K562	blood:	n/a	n/a
39	MYC	chr6:33407745-33408746	K562	blood:	n/a	n/a
40	MYC	chr6:33408513-33408544	K562	blood:	n/a	n/a
41	MYC	chr6:33408371-33408676	K562	blood:	n/a	n/a
42	MYC	chr6:33413292-33413346	NB4	blood:	n/a	n/a
43	MYC	chr6:33421563-33422591	MCF10A-Er-Src	breast:	n/a	n/a
44	NRF1	chr6:33408453-33408592	K562	blood:	n/a	n/a
45	PML	chr6:33421526-33422839	K562	blood:	n/a	n/a
46	PML	chr6:33421566-33422697	K562	blood:	n/a	n/a
47	POLR2A	chr6:33417598-33418944	K562	blood:	n/a	n/a
48	POLR2A	chr6:33412543-33412610	HepG2	liver:	n/a	n/a
49	POLR2A	chr6:33420362-33420605	H1-hESC	embryonic stem cell:	n/a	n/a
50	POLR2A	chr6:33419159-33419608	H1-hESC	embryonic stem cell:	n/a	n/a

(count:1956 , 50 per page) page: 1 2 3 4 5 6 7 ... 40

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:33419653-33419703	HCPEpiC	choroid plexus:	n/a
2	chr6:33418814-33418864	HCT-116	colon:	n/a
3	chr6:33421180-33421230	HMEC	breast:	n/a
4	chr6:33409448-33409498	HCF	heart:	n/a
5	chr6:33419653-33419703	HCPEpiC	choroid plexus:	n/a
6	chr6:33418814-33418864	HCT-116	colon:	n/a
7	chr6:33421180-33421230	HMEC	breast:	n/a
8	chr6:33409448-33409498	HCF	heart:	n/a
9	chr6:33420121-33420171	HEK293	kidney:	embryo
10	chr6:33418814-33418864	Hela-S3	cervix:	n/a
11	chr6:33419496-33419546	SK-N-MC	brain:	n/a
12	chr6:33418310-33418360	HepG2	liver:	n/a
13	chr6:33419510-33419560	AG09319	gingival:	n/a
14	chr6:33419646-33419696	AG09309	skin:	n/a
15	chr6:33421180-33421230	CMK	blood:	n/a
16	chr6:33415267-33415317	SAEC	small airway:	n/a
17	chr6:33419633-33419683	HIPEpiC	eye:	n/a
18	chr6:33409399-33409449	HL-60	blood:	n/a
19	chr6:33419766-33419816	HPAEpiC	pulmonary alveolar:	n/a
20	chr6:33419510-33419560	AG09309	skin:	n/a
21	chr6:33419140-33419190	U87	brain:	n/a
22	chr6:33421180-33421230	GM19239	blood:	n/a
23	chr6:33421476-33421526	Caco-2	colon:	n/a
24	chr6:33419573-33419623	HRPEpiC	eye:	n/a
25	chr6:33419512-33419562	HRCEpiC	kidney:	n/a
26	chr6:33419571-33419621	ECC-1	luminal epithelium:	n/a
27	chr6:33419573-33419623	RPTEC	kidney:	n/a
28	chr6:33419766-33419816	PrEC	prostate:	n/a
29	chr6:33419580-33419630	SK-N-SH	brain:	n/a
30	chr6:33419656-33419706	GM19239	blood:	n/a
31	chr6:33419766-33419816	PFSK-1	brain:	n/a
32	chr6:33419510-33419560	ECC-1	luminal epithelium:	n/a
33	chr6:33419571-33419621	AG09319	gingival:	n/a
34	chr6:33419653-33419703	U87	brain:	n/a
35	chr6:33414363-33414413	HNPCEpiC	eye:	n/a
36	chr6:33419353-33419403	RPTEC	kidney:	n/a
37	chr6:33418814-33418864	GM12892	blood:	n/a
38	chr6:33409448-33409498	LNCaP	prostate:	n/a
39	chr6:33420121-33420171	HCT-116	colon:	n/a
40	chr6:33421468-33421518	PrEC	prostate:	n/a
41	chr6:33419353-33419403	AG09309	skin:	n/a
42	chr6:33421468-33421518	ProgFib	skin:	n/a
43	chr6:33419633-33419683	PFSK-1	brain:	n/a
44	chr6:33419353-33419403	Hela-S3	cervix:	n/a
45	chr6:33419573-33419623	ProgFib	skin:	n/a
46	chr6:33419633-33419683	CMK	blood:	n/a
47	chr6:33421468-33421518	LNCaP	prostate:	n/a
48	chr6:33416652-33416702	Jurkat	blood:	n/a
49	chr6:33419573-33419623	CMK	blood:	n/a
50	chr6:33419656-33419706	AG09309	skin:	n/a

(count:24 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:33357200..33360290-chr6:33405779..33409122,3	K562	blood:
2	chr6:33402335..33405767-chr6:33416394..33418965,3	MCF-7	breast:
3	chr6:33407430..33409237-chr6:33415034..33417664,3	MCF-7	breast:
4	chr6:33357170..33359461-chr6:33419565..33421602,2	K562	blood:
5	chr6:33416427..33418165-chr6:33432976..33435399,2	K562	blood:
6	chr6:33385453..33389637-chr6:33419628..33424957,5	MCF-7	breast:
7	chr6:33398677..33403495-chr6:33419995..33423723,6	K562	blood:
8	chr6:33242343..33245009-chr6:33406887..33409853,3	K562	blood:
9	chr6:33399707..33401893-chr6:33408144..33410005,2	MCF-7	breast:
10	chr6:33409867..33413069-chr6:33413724..33418107,6	MCF-7	breast:
11	chr6:33393532..33395218-chr6:33409993..33412120,3	MCF-7	breast:
12	chr6:33406190..33414491-chr6:33419287..33424467,10	MCF-7	breast:
13	chr6:33245204..33246812-chr6:33420469..33423462,2	MCF-7	breast:
14	chr6:33392449..33400629-chr6:33419013..33424035,12	MCF-7	breast:
15	chr6:33407586..33409275-chr6:33483578..33485423,2	K562	blood:
16	chr6:33395899..33401993-chr6:33420102..33423796,11	MCF-7	breast:
17	chr6:33381847..33384907-chr6:33420236..33423106,3	MCF-7	breast:
18	chr6:33404069..33406750-chr6:33407909..33409800,2	MCF-7	breast:
19	chr6:33358627..33361285-chr6:33416169..33418601,2	MCF-7	breast:
20	chr6:33392146..33394863-chr6:33415963..33418099,3	MCF-7	breast:
21	chr6:33407430..33409237-chr6:33415034..33417664,3	MCF-7	breast:
22	chr17:57917402..57920135-chr6:33409836..33411745,2	MCF-7	breast:
23	chr19:5689875..5690838-chr6:33420626..33421397,2	Hela-S3	cervix:
24	chr6:33406190..33414491-chr6:33419287..33424467,10	MCF-7	breast:

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	SYNGAP1	hsa-miR-30c-5p	chr6:33421424-33421446

Variant related genes	Relation type
SYNGAP1	TF binding region
ZBTB9	TF binding region
SYNGAP1	CpG island
ZBTB9	CpG island
ENSG00000231500	chromatin interactions
ENSG00000197283	chromatin interactions
ENSG00000225644	chromatin interactions
ENSG00000130255	chromatin interactions
ENSG00000237649	chromatin interactions
ENSG00000199004	chromatin interactions
ENSG00000235863	chromatin interactions
ENSG00000264085	chromatin interactions
ENSG00000213588	chromatin interactions
ENSG00000112511	chromatin interactions
ENSG00000112514	chromatin interactions

Extended variants
information (count: 399 )
Associated
traits (count: 111 )

Variant overlapped rSNPs/rCNVs (count:399 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs411136	chr6:33408542-33408543	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers Flanking Active TSS	Chromatin interactive region	7 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs576589974	chr6:33408557-33408558	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers Flanking Active TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
3	rs121918316	chr6:33408564-33408565	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers Flanking Active TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
4	rs571865766	chr6:33408599-33408600	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers Flanking Active TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
5	rs150153477	chr6:33408605-33408606	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
6	rs77934848	chr6:33408632-33408633	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
7	rs149727287	chr6:33408641-33408642	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
8	rs532636247	chr6:33408657-33408658	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
9	rs75579703	chr6:33408680-33408681	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
10	rs140022772	chr6:33408713-33408714	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
11	rs192497085	chr6:33408717-33408718	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
12	rs572578854	chr6:33408764-33408765	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
13	rs199669547	chr6:33408778-33408779	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
14	rs541494835	chr6:33408810-33408811	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
15	rs567534561	chr6:33408844-33408845	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
16	rs564457900	chr6:33408859-33408860	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
17	rs369976170	chr6:33408864-33408865	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
18	rs146262788	chr6:33408871-33408872	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
19	rs531446172	chr6:33408886-33408887	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
20	rs541515697	chr6:33408890-33408891	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
21	rs376847674	chr6:33408891-33408892	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
22	rs377338011	chr6:33408900-33408901	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
23	rs139133669	chr6:33408902-33408903	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
24	rs368864415	chr6:33408905-33408906	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
25	rs571255450	chr6:33408906-33408907	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
26	rs561866153	chr6:33408915-33408916	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
27	rs538693715	chr6:33408918-33408919	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
28	rs145406441	chr6:33408971-33408972	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
29	rs373857862	chr6:33408998-33408999	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
30	rs372231550	chr6:33409008-33409009	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
31	rs572418133	chr6:33409029-33409030	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
32	rs57365292	chr6:33409052-33409053	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
33	rs147668681	chr6:33409083-33409084	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
34	rs536234142	chr6:33409085-33409086	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
35	rs375292597	chr6:33409134-33409135	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
36	rs376826632	chr6:33409176-33409177	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
37	rs371178528	chr6:33409254-33409255	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
38	rs542626097	chr6:33409257-33409258	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
39	rs372141222	chr6:33409263-33409264	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
40	rs113487504	chr6:33409266-33409267	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
41	rs185437254	chr6:33409328-33409329	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
42	rs374219418	chr6:33409335-33409336	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
43	rs149131236	chr6:33409360-33409361	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
44	rs143401233	chr6:33409363-33409364	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
45	rs543705054	chr6:33409367-33409368	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
46	rs559061651	chr6:33409399-33409400	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
47	rs577278005	chr6:33409442-33409443	Weak transcription Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
48	rs151334677	chr6:33409449-33409450	Weak transcription Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
49	rs377301201	chr6:33409484-33409485	Weak transcription Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
50	rs373755298	chr6:33409498-33409499	Weak transcription Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:111)

Disease	PMID	Source
Follicular lymphoma	20505157	CNVD
Glioblastoma multiforme	21080181	CNVD
Ewing''s sarcoma	21437220	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Leukemia	21518781	CNVD
Cancer	21637783	CNVD
Facial dysmorphism	22105932	CNVD
Medulloblastoma	21979893	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Endometrial cancer	22040021	CNVD
Acute myeloid leukemia	16864856	CNVD
Breast cancer	21264507	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	16751803	CNVD
Bladder cancer	19088036	CNVD
Wilms tumour	21544195	CNVD
Uveal melanoma	21693616	CNVD
Biliary cancer	19435499	CNVD
Malaria	21533027	CNVD
Retinoblastoma	19183342	CNVD
Acute myeloid leukemia	20729466	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21858162	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	21448237	CNVD
Melanoma	18172304	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Hepatocellular carcinoma	16750200	CNVD
Autism	22495311	CNVD
Cancer	16790693	CNVD
Cervical cancer	21062161	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Systemic lupus erythematosus	17503323	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Urothelial carcinoma	18382360	CNVD
Cancer	21183584	CNVD
Hodgkin''s lymphoma	17606441	CNVD
small cell lung cancer	20016488	CNVD
Renal cell carcinoma	18765545	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Gastric cancer	17908304	CNVD
Metanephric adenoma	20802469	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Schizophrenia	19571808	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Neuroblastoma	16790693	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
abnormal development	18461090	CNVD
Breast cancer	16397240	CNVD
Retinoblastoma	22278416	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Systemic lupus erythematosus	20877625	CNVD
Cleidocranial dysplasia	18696259	CNVD
Holoprosencephaly	21359414	CNVD
Liposarcoma	21253554	CNVD
Uveal melanoma	20484589	CNVD
Fibroblasts	20926602	CNVD
Systemic lupus erythematosus	19279649	CNVD
Retinoblastoma	16790693	CNVD
Acute myocardial infarction	18032375	CNVD
Renal cell carcinoma	19150565	CNVD
Systemic lupus erythematosus	19591781	CNVD
Attention deficit hyperactivity disorder	19287146	CNVD
Autism	19287146	CNVD
Erythema nodosum in leprosy	19287146	CNVD
Henoch-schoenlein purpura	19287146	CNVD
Liver cirrhosis	19287146	CNVD
Systemic lupus erythematosus	19287146	CNVD
Autoimmune disease	19135723	CNVD
Congenital adrenal hyperplasia	18478071	CNVD
Systemic lupus erythematosus	19287147	CNVD
Osteosarcoma	16790693	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Cancer	22183965	CNVD
Melanoma	22183965	CNVD
Myelofibrosis	22110671	CNVD
Incontinentia Pigmenti	22033527	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Encephalopathy	20692195	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Immune disease	17576883	CNVD
Multiple myeloma	16616336	CNVD
Lung cancer	18438408	CNVD
Glioblastoma multiforme	21138945	CNVD
Anaplastic thyroid cancer	18753363	CNVD
Breast cancer	21364760	CNVD
Urothelial carcinoma	21177765	CNVD
Autism	20964600	CNVD
Autism	20531469	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:587 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:33396600-33416000	Weak transcription	Pancreas	Pancrea
2	chr6:33399400-33421200	Weak transcription	HMEC	breast
3	chr6:33399400-33421600	Weak transcription	Stomach Mucosa	stomach
4	chr6:33399600-33409200	Weak transcription	Small Intestine	intestine
5	chr6:33399600-33421400	Weak transcription	HUVEC	blood vessel
6	chr6:33399800-33421400	Weak transcription	A549	lung
7	chr6:33400000-33412800	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
8	chr6:33400000-33418000	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
9	chr6:33400000-33420600	Strong transcription	Brain Germinal Matrix	brain
10	chr6:33400800-33412800	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--
11	chr6:33401200-33420800	Strong transcription	Fetal Brain Female	brain
12	chr6:33401400-33417600	Strong transcription	Primary T cells fromperipheralblood	blood
13	chr6:33401400-33418800	Strong transcription	Breast Myoepithelial Primary Cells	Breast
14	chr6:33401400-33421400	Weak transcription	Right Atrium	heart
15	chr6:33401600-33416600	Strong transcription	Cortex derived primary cultured neurospheres	brain
16	chr6:33402000-33417600	Strong transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
17	chr6:33402000-33418000	Strong transcription	Brain Dorsolateral Prefrontal Cortex	brain
18	chr6:33402000-33418000	Strong transcription	NHLF	lung
19	chr6:33402000-33418200	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
20	chr6:33402000-33420600	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
21	chr6:33402200-33417400	Strong transcription	Primary T helper cells fromperipheralblood	blood
22	chr6:33402200-33417400	Strong transcription	Thymus	Thymus
23	chr6:33402200-33418200	Strong transcription	Fetal Muscle Leg	muscle
24	chr6:33402200-33418600	Strong transcription	Dnd41	blood
25	chr6:33402200-33420000	Strong transcription	Fetal Thymus	thymus
26	chr6:33402200-33420800	Weak transcription	Skeletal Muscle Female	skeletal muscle
27	chr6:33402400-33420800	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
28	chr6:33402600-33417600	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
29	chr6:33402600-33420000	Strong transcription	HUES64 Cell Line	embryonic stem cell
30	chr6:33402600-33420400	Strong transcription	Fetal Stomach	stomach
31	chr6:33402600-33421400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
32	chr6:33402800-33411000	Strong transcription	Brain Hippocampus Middle	brain
33	chr6:33402800-33417200	Strong transcription	Fetal Intestine Small	intestine
34	chr6:33402800-33417400	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
35	chr6:33402800-33417600	Strong transcription	iPS DF 6.9 Cell Line	embryonic stem cell
36	chr6:33402800-33417600	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
37	chr6:33402800-33417600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
38	chr6:33402800-33417800	Strong transcription	Primary T cells from cord blood	blood
39	chr6:33402800-33417800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
40	chr6:33402800-33418400	Strong transcription	Primary hematopoietic stem cells short term culture	blood
41	chr6:33402800-33418600	Strong transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
42	chr6:33402800-33418600	Strong transcription	iPS-15b Cell Line	embryonic stem cell
43	chr6:33402800-33419000	Strong transcription	HUES48 Cell Line	embryonic stem cell
44	chr6:33402800-33420000	Strong transcription	H9 Cell Line	embryonic stem cell
45	chr6:33402800-33420000	Strong transcription	HUES6 Cell Line	embryonic stem cell
46	chr6:33402800-33420000	Strong transcription	iPS-18 Cell Line	embryonic stem cell
47	chr6:33402800-33420200	Strong transcription	H1 Cell Line	embryonic stem cell
48	chr6:33402800-33420200	Strong transcription	Fetal Muscle Trunk	muscle
49	chr6:33403000-33409800	Strong transcription	Placenta	Placenta
50	chr6:33403000-33410800	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain

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