Variant report

Variant	esv3359258
Chromosome Location	chr3:67589615-67828274
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1960)
CpG islands
(count:1282)
Chromatin interactive
region (count:70)
LncRNA
region (count:25)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1960 , 50 per page) page: 1 2 3 4 5 6 7 ... 40

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr3:67661892-67662146	HepG2	liver:	n/a	n/a
2	ARID3A	chr3:67704355-67704636	HepG2	liver:	n/a	n/a
3	ARID3A	chr3:67590641-67590915	HepG2	liver:	n/a	n/a
4	ARID3A	chr3:67700651-67700719	K562	blood:	n/a	n/a
5	ARID3A	chr3:67674684-67674851	HepG2	liver:	n/a	n/a
6	ARID3A	chr3:67660880-67661161	HepG2	liver:	n/a	n/a
7	ARID3A	chr3:67645957-67646226	HepG2	liver:	n/a	n/a
8	ARID3A	chr3:67697613-67699132	HepG2	liver:	n/a	n/a
9	ATF1	chr3:67816061-67816270	K562	blood:	n/a	n/a
10	ATF2	chr3:67703602-67704684	GM12878	blood:	n/a	n/a
11	ATF2	chr3:67705875-67706696	GM12878	blood:	n/a	n/a
12	ATF2	chr3:67609491-67610034	GM12878	blood:	n/a	n/a
13	ATF2	chr3:67703532-67704260	GM12878	blood:	n/a	n/a
14	ATF2	chr3:67705980-67706580	GM12878	blood:	n/a	n/a
15	ATF2	chr3:67735890-67736348	GM12878	blood:	n/a	n/a
16	ATF3	chr3:67697659-67698348	A549	lung:	n/a	n/a
17	ATF3	chr3:67697628-67698306	A549	lung:	n/a	n/a
18	BACH1	chr3:67637854-67637890	K562	blood:	n/a	n/a
19	BATF	chr3:67735954-67736214	GM12878	blood:	n/a	n/a
20	BATF	chr3:67691889-67692087	GM12878	blood:	n/a	n/a
21	BATF	chr3:67705950-67706326	GM12878	blood:	n/a	n/a
22	BATF	chr3:67705916-67706474	GM12878	blood:	n/a	n/a
23	BCL11A	chr3:67703945-67704174	GM12878	blood:	n/a	n/a
24	BCL11A	chr3:67705928-67706647	GM12878	blood:	n/a	n/a
25	BCL11A	chr3:67706288-67706603	GM12878	blood:	n/a	n/a
26	BCL3	chr3:67697742-67698369	A549	lung:	n/a	n/a
27	BCL3	chr3:67704760-67705150	GM12878	blood:	n/a	n/a
28	BCL3	chr3:67649711-67649960	GM12878	blood:	n/a	n/a
29	BCL3	chr3:67697182-67698486	A549	lung:	n/a	chr3:67697209-67697218
30	BCL3	chr3:67649604-67650002	GM12878	blood:	n/a	n/a
31	BCLAF1	chr3:67705883-67706721	GM12878	blood:	n/a	n/a
32	BCLAF1	chr3:67705939-67706624	GM12878	blood:	n/a	n/a
33	BCLAF1	chr3:67735803-67736390	GM12878	blood:	n/a	chr3:67736181-67736190 chr3:67736175-67736184
34	BHLHE40	chr3:67697679-67698327	HepG2	liver:	n/a	n/a
35	BHLHE40	chr3:67592929-67593210	HepG2	liver:	n/a	n/a
36	BHLHE40	chr3:67691490-67691539	GM12878	blood:	n/a	n/a
37	BHLHE40	chr3:67735959-67736284	GM12878	blood:	n/a	n/a
38	BHLHE40	chr3:67668012-67668248	GM12878	blood:	n/a	n/a
39	BHLHE40	chr3:67703349-67705323	GM12878	blood:	n/a	chr3:67704778-67704794 chr3:67704889-67704905 chr3:67704881-67704897 chr3:67704875-67704891 chr3:67704716-67704732 chr3:67704724-67704740 chr3:67704897-67704913
40	BHLHE40	chr3:67706029-67706854	GM12878	blood:	n/a	n/a
41	BHLHE40	chr3:67704199-67705234	K562	blood:	n/a	chr3:67704778-67704794 chr3:67704889-67704905 chr3:67704881-67704897 chr3:67704875-67704891 chr3:67704716-67704732 chr3:67704724-67704740 chr3:67704897-67704913
42	BHLHE40	chr3:67704306-67705271	HepG2	liver:	n/a	chr3:67704778-67704794 chr3:67704889-67704905 chr3:67704881-67704897 chr3:67704875-67704891 chr3:67704716-67704732 chr3:67704724-67704740 chr3:67704897-67704913
43	BHLHE40	chr3:67825040-67825316	HepG2	liver:	n/a	n/a
44	BHLHE40	chr3:67682225-67682331	GM12878	blood:	n/a	n/a
45	BRCA1	chr3:67703993-67704482	Hela-S3	cervix:	n/a	n/a
46	BRCA1	chr3:67697772-67698247	Hela-S3	cervix:	n/a	n/a
47	BRCA1	chr3:67704914-67705118	HepG2	liver:	n/a	n/a
48	BRCA1	chr3:67705494-67705621	HepG2	liver:	n/a	n/a
49	CBX3	chr3:67697746-67698356	HCT-116	colon:	n/a	n/a
50	CBX3	chr3:67697733-67698356	HCT-116	colon:	n/a	n/a

(count:1282 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:67704629-67704679	CMK	blood:	n/a
2	chr3:67704629-67704679	CMK	blood:	n/a
3	chr3:67705222-67705272	SK-N-MC	brain:	n/a
4	chr3:67701995-67702045	HRPEpiC	eye:	n/a
5	chr3:67705285-67705335	GM19239	blood:	n/a
6	chr3:67706352-67706402	GM12891	blood:	n/a
7	chr3:67706352-67706402	Caco-2	colon:	n/a
8	chr3:67754377-67754427	GM12878	blood:	n/a
9	chr3:67754377-67754427	MCF10A-Er-Src	breast:	n/a
10	chr3:67705048-67705098	GM12891	blood:	n/a
11	chr3:67699305-67699355	HRCEpiC	kidney:	n/a
12	chr3:67706047-67706097	BE2_C	brain:	n/a
13	chr3:67705228-67705278	AG04449	skin:	fetal
14	chr3:67706352-67706402	ovcar-3	ovarian:	n/a
15	chr3:67701995-67702045	HEEpiC	esophagus:	n/a
16	chr3:67704970-67705020	Caco-2	colon:	n/a
17	chr3:67704244-67704294	A549	lung:	n/a
18	chr3:67706320-67706370	A549	lung:	n/a
19	chr3:67706500-67706550	NHDF-neo	bronchial:	n/a
20	chr3:67705285-67705335	GM06990	blood:	n/a
21	chr3:67706047-67706097	HNPCEpiC	eye:	n/a
22	chr3:67691965-67692015	AG09309	skin:	n/a
23	chr3:67706352-67706402	HIPEpiC	eye:	n/a
24	chr3:67747930-67747980	Jurkat	blood:	n/a
25	chr3:67704244-67704294	NHDF-neo	bronchial:	n/a
26	chr3:67774792-67774842	NH-A	brain:	n/a
27	chr3:67699305-67699355	HepG2	liver:	n/a
28	chr3:67704244-67704294	SKMC	muscle:	n/a
29	chr3:67706500-67706550	H1-hESC	embryonic stem cell:	embryo
30	chr3:67705048-67705098	H1-hESC	embryonic stem cell:	embryo
31	chr3:67707729-67707779	GM12878	blood:	n/a
32	chr3:67706320-67706370	HIPEpiC	eye:	n/a
33	chr3:67707729-67707779	PANC-1	pancreas:	n/a
34	chr3:67705048-67705098	GM19239	blood:	n/a
35	chr3:67704970-67705020	GM06990	blood:	n/a
36	chr3:67706352-67706402	AG04449	skin:	fetal
37	chr3:67705228-67705278	ProgFib	skin:	n/a
38	chr3:67698057-67698107	IMR90	lung:	fetal
39	chr3:67704970-67705020	U87	brain:	n/a
40	chr3:67707729-67707779	AG10803	skin:	n/a
41	chr3:67701995-67702045	GM12892	blood:	n/a
42	chr3:67754377-67754427	Jurkat	blood:	n/a
43	chr3:67704629-67704679	HCF	heart:	n/a
44	chr3:67698057-67698107	HEK293	kidney:	embryo
45	chr3:67705222-67705272	Jurkat	blood:	n/a
46	chr3:67754377-67754427	BJ	skin:	n/a
47	chr3:67691965-67692015	NH-A	brain:	n/a
48	chr3:67704244-67704294	GM12891	blood:	n/a
49	chr3:67774792-67774842	H1-hESC	embryonic stem cell:	embryo
50	chr3:67704629-67704679	SK-N-SH	brain:	n/a

(count:70 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr3:67658685..67661216-chr3:67677241..67680010,2	MCF-7	breast:
2	chr3:67703511..67705950-chr3:67707757..67710828,3	MCF-7	breast:
3	chr3:67703980..67705927-chr3:67710153..67712028,2	K562	blood:
4	chr3:67687185..67689279-chr3:67695824..67697834,2	K562	blood:
5	chr3:67693669..67696019-chr3:67696200..67698241,3	MCF-7	breast:
6	chr3:67689171..67691000-chr3:67691714..67693901,2	MCF-7	breast:
7	chr3:67707583..67709942-chr3:67710022..67712395,2	K562	blood:
8	chr3:67693692..67697649-chr3:67698032..67705100,9	K562	blood:
9	chr3:67622636..67625253-chr3:67625381..67627788,2	MCF-7	breast:
10	chr3:67685734..67687537-chr3:67689590..67691378,2	K562	blood:
11	chr3:67703884..67706794-chr3:67715765..67717905,2	MCF-7	breast:
12	chr3:67658685..67661216-chr3:67677241..67680010,2	MCF-7	breast:
13	chr3:67697874..67699560-chr3:67705440..67708186,2	K562	blood:
14	chr3:67693746..67699726-chr3:67701571..67705130,8	K562	blood:
15	chr3:67683377..67686449-chr3:67703484..67706242,3	K562	blood:
16	chr3:67669767..67672572-chr3:67674238..67677122,3	K562	blood:
17	chr2:43448399..43449108-chr3:67720703..67721562,2	MCF-7	breast:
18	chr3:67794644..67797573-chr3:67799794..67802421,2	K562	blood:
19	chr3:67646494..67648769-chr3:67650220..67652674,2	MCF-7	breast:
20	chr3:67690704..67693010-chr3:67695548..67697113,2	K562	blood:
21	chr3:67635502..67637336-chr3:67638611..67641074,2	K562	blood:
22	chr3:67686748..67688794-chr3:67696396..67698121,2	MCF-7	breast:
23	chr3:67697874..67699560-chr3:67705440..67708186,2	K562	blood:
24	chr3:67690704..67693010-chr3:67695548..67697113,2	K562	blood:
25	chr3:67701996..67704573-chr3:67817178..67820032,3	MCF-7	breast:
26	chr3:67661874..67664225-chr3:67709456..67711334,2	MCF-7	breast:
27	chr3:67696995..67702204-chr3:67702925..67706326,7	MCF-7	breast:
28	chr3:67701996..67704573-chr3:67817178..67820032,3	MCF-7	breast:
29	chr3:67639021..67641563-chr3:67644439..67647690,3	K562	blood:
30	chr3:67626314..67629227-chr3:67636253..67638089,2	MCF-7	breast:
31	chr3:67680927..67683054-chr3:67703449..67705056,2	MCF-7	breast:
32	chr3:67635502..67637336-chr3:67638611..67641074,2	K562	blood:
33	chr3:67821892..67822812-chr3:67840239..67841219,2	K562	blood:
34	chr3:67707583..67709942-chr3:67710022..67712395,2	K562	blood:
35	chr3:67644182..67646267-chr3:67702951..67705002,2	MCF-7	breast:
36	chr3:67794644..67797573-chr3:67799794..67802421,2	K562	blood:
37	chr3:67646494..67648769-chr3:67650220..67652674,2	MCF-7	breast:
38	chr3:67669767..67672572-chr3:67674238..67677122,3	K562	blood:
39	chr3:67686165..67687924-chr3:67690754..67692327,2	K562	blood:
40	chr3:67639021..67641563-chr3:67644439..67647690,3	K562	blood:
41	chr3:67661740..67663579-chr3:67665104..67667136,2	K562	blood:
42	chr3:67603334..67606300-chr3:67607954..67610100,2	K562	blood:
43	chr3:67685734..67687537-chr3:67689590..67691378,2	K562	blood:
44	chr3:67673373..67676039-chr3:67678094..67679786,2	K562	blood:
45	chr3:67644182..67646267-chr3:67702951..67705002,2	MCF-7	breast:
46	chr16:47239252..47239752-chr3:67770876..67771427,2	Hela-S3	cervix:
47	chr3:67686165..67687924-chr3:67690754..67692327,2	K562	blood:
48	chr3:67661740..67663579-chr3:67665104..67667136,2	K562	blood:
49	chr3:67661874..67664225-chr3:67709456..67711334,2	MCF-7	breast:
50	chr3:67692723..67696784-chr3:67696803..67701487,5	K562	blood:

(count:25 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FAM19A1-1	chr3:67720240-67720333	NR_109992
2	lnc-FAM19A1-1	chr3:67800277-67800394	ENSG00000241316
3	lnc-FAM19A1-1	chr3:67705182-67705526	ENSG00000241316
4	lnc-FAM19A1-1	chr3:67721253-67721428	NR_109992
5	lnc-FAM19A1-1	chr3:67718671-67718701	ENSG00000241316
6	lnc-FAM19A1-1	chr3:67720240-67720333	ENSG00000241316
7	lnc-FAM19A1-3	chr3:67717729-67717836	NONHSAT090322
8	lnc-FAM19A1-1	chr3:67705121-67705526	ENSG00000241316
9	lnc-FAM19A1-1	chr3:67797195-67799050	NONHSAT090319
10	lnc-FAM19A1-1	chr3:67720240-67720333	ENSG00000241316
11	lnc-FAM19A1-1	chr3:67721306-67721428	ENSG00000241316
12	lnc-FAM19A1-2	chr3:67803943-67804118	l_2384_chr3:67787798-67880076_thyroid
13	lnc-FAM19A1-1	chr3:67721253-67721428	ENSG00000241316
14	lnc-FAM19A1-2	chr3:67802930-67803023	l_2384_chr3:67787798-67880076_thyroid
15	lnc-FAM19A1-1	chr3:67705121-67705526	NR_109992
16	lnc-FAM19A1-1	chr3:67720240-67720333	ENSG00000241316
17	lnc-FAM19A1-1	chr3:67705040-67705526	NONHSAT090319
18	lnc-FAM19A1-2	chr3:67787799-67788216	l_2384_chr3:67787798-67880076_thyroid
19	lnc-FAM19A1-1	chr3:67721253-67721428	ENSG00000241316
20	lnc-FAM19A1-2	chr3:67801340-67801391	l_2384_chr3:67787798-67880076_thyroid
21	lnc-FAM19A1-1	chr3:67797195-67797381	ENSG00000241316
22	lnc-FAM19A1-1	chr3:67800838-67801093	ENSG00000241316
23	lnc-FAM19A1-3	chr3:67717423-67717621	NONHSAT090322
24	lnc-FAM19A1-1	chr3:67797195-67797534	ENSG00000241316
25	lnc-FAM19A1-1	chr3:67720240-67721428	NONHSAT090319

No data

Variant related genes	Relation type
ENSG00000241316	TF binding region
SUCLG2	TF binding region
ENSG00000241316	CpG island
SUCLG2	CpG island
ENSG00000185246	chromatin interactions
ENSG00000241316	chromatin interactions
ENSG00000163377	chromatin interactions
ENSG00000103852	chromatin interactions
ENSG00000249163	chromatin interactions
ENSG00000131669	chromatin interactions
ENSG00000168904	chromatin interactions
ENSG00000172340	chromatin interactions
ENSG00000260233	chromatin interactions

Extended variants
information (count: 8781 )
Associated
traits (count: 84 )

Variant overlapped rSNPs/rCNVs (count:8781 , 50 per page) page: 1 2 3 4 5 6 7 ... 176

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs528611340	chr3:67589684-67589685	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs138180965	chr3:67589690-67589691	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs149133626	chr3:67589695-67589696	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs530924148	chr3:67589717-67589718	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs550953813	chr3:67589721-67589722	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs143400170	chr3:67589764-67589765	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs148369046	chr3:67589775-67589776	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs549215414	chr3:67589776-67589777	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs565853690	chr3:67589779-67589780	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs541037303	chr3:67589792-67589793	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs544999759	chr3:67589832-67589833	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs557833593	chr3:67589843-67589844	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs6774766	chr3:67589850-67589851	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs536660754	chr3:67589851-67589852	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs556495220	chr3:67589857-67589858	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs142144537	chr3:67589878-67589879	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs146350356	chr3:67589911-67589912	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs138405273	chr3:67589919-67589920	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs190201056	chr3:67589952-67589953	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs545211018	chr3:67590013-67590014	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs182699501	chr3:67590030-67590031	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs141689109	chr3:67590061-67590062	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs186599785	chr3:67590064-67590065	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs150739154	chr3:67590066-67590067	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs139058230	chr3:67590067-67590068	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs191509884	chr3:67590080-67590081	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs185419781	chr3:67590081-67590082	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs528282057	chr3:67590155-67590156	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs551249261	chr3:67590166-67590167	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs571324603	chr3:67590190-67590191	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs149869225	chr3:67590225-67590226	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs144168837	chr3:67590270-67590271	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs566898428	chr3:67590283-67590284	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs536593927	chr3:67590367-67590368	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs188985800	chr3:67590409-67590410	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs573416576	chr3:67590437-67590438	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs545585685	chr3:67590438-67590439	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs140562555	chr3:67590444-67590445	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs371528659	chr3:67590532-67590533	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs544410548	chr3:67590545-67590546	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs561100760	chr3:67590650-67590651	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs144423381	chr3:67590678-67590679	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs193126802	chr3:67590716-67590717	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs542986401	chr3:67590724-67590725	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs566969488	chr3:67590739-67590740	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs559609523	chr3:67590742-67590743	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs528330151	chr3:67590757-67590758	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs551578285	chr3:67590764-67590765	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs564912592	chr3:67590787-67590788	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs72924913	chr3:67590822-67590823	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:84)

Disease	PMID	Source
Melanoma	18172304	CNVD
Cervical cancer	21062161	CNVD
Hirschsprung''s Disease	21712996	CNVD
Acute myeloid leukemia	20729466	CNVD
Glioblastoma multiforme	21080181	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Insulin resistance	16721378	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	21484798	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Oral cancer	19627613	CNVD
Renal cell carcinoma	19461508	CNVD
Epithelial cancer	22065749	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Acute myeloid leukemia	16864856	CNVD
Liposarcoma	21253554	CNVD
Basal cell lymphoma	21115979	CNVD
Endometrial cancer	22040021	CNVD
Pancreatic endocrine tumor	20981439	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	17387387	CNVD
Oral cancer	21386901	CNVD
Cutaneous squamous cell carcinomas	19131950	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Retinoblastoma	21504564	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Renal cell carcinoma	21668985	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Lung cancer	18438408	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	17603634	CNVD
Esophageal cancer	20955586	CNVD
Breast cancer	17133270	CNVD
Uveal melanoma	20484589	CNVD
Autism	22495311	CNVD
Acute myeloid leukemia	21251322	CNVD
Hepatocellular carcinoma	16750200	CNVD
Cancer	21183584	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Bipolar disorder	20877625	CNVD
Bipolar disorder	21956041	CNVD
Bipolar disorder	22241247	CNVD
Biliary cancer	18923514	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Squamous cell cancer	20885788	CNVD
Breast cancer	16608533	CNVD
Prostate cancer	21965145	CNVD
Cancer	21129771	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	19490591	CNVD
Autism	18414403	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Non-small cell lung cancer	20864512	CNVD
Metastatic melanoma	17975146	CNVD
Breast cancer	21509527	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Autism	22102821	CNVD
Myelofibrosis	22110671	CNVD
Mental retardation	21062444	CNVD
Prostate cancer	17217626	CNVD
Urothelial cell carcinoma	18451213	CNVD
Alzheimer''s disease	22166940	CNVD
Mental retardation	20848658	CNVD
Breast cancer	17142309	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
Breast cancer	21364760	CNVD
lymphocytic leukemia	21291569	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:3371 , 50 per page) page: 1 2 3 4 5 6 7 ... 68

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:67560600-67620800	Weak transcription	Esophagus	oesophagus
2	chr3:67565600-67595800	Weak transcription	Fetal Kidney	kidney
3	chr3:67568000-67590600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr3:67578200-67600400	Weak transcription	Lung	lung
5	chr3:67578200-67612400	Weak transcription	Spleen	Spleen
6	chr3:67578200-67634600	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
7	chr3:67578400-67593800	Weak transcription	Fetal Intestine Small	intestine
8	chr3:67578600-67601800	Weak transcription	Left Ventricle	heart
9	chr3:67579200-67603400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
10	chr3:67579200-67608800	Weak transcription	Sigmoid Colon	Sigmoid Colon
11	chr3:67579200-67620600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
12	chr3:67579400-67590800	Weak transcription	Fetal Stomach	stomach
13	chr3:67579400-67591000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
14	chr3:67579400-67598200	Weak transcription	Aorta	Aorta
15	chr3:67579400-67600600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
16	chr3:67579400-67623000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
17	chr3:67579400-67633800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
18	chr3:67579400-67657600	Weak transcription	Pancreas	Pancrea
19	chr3:67579600-67601000	Weak transcription	Duodenum Mucosa	Duodenum
20	chr3:67579600-67601800	Weak transcription	Fetal Intestine Large	intestine
21	chr3:67579600-67601800	Weak transcription	Ovary	ovary
22	chr3:67580000-67606400	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
23	chr3:67580600-67591200	Weak transcription	Primary T cells from cord blood	blood
24	chr3:67580800-67620200	Weak transcription	GM12878-XiMat	blood
25	chr3:67582000-67590800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
26	chr3:67582000-67601600	Weak transcription	Rectal Mucosa Donor 31	rectum
27	chr3:67582200-67637000	Weak transcription	Rectal Smooth Muscle	rectum
28	chr3:67582400-67596400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
29	chr3:67582400-67609000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
30	chr3:67582400-67620400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
31	chr3:67582600-67612000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
32	chr3:67584400-67601600	Weak transcription	A549	lung
33	chr3:67586000-67591000	Weak transcription	Psoas Muscle	Psoas
34	chr3:67586200-67597600	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
35	chr3:67587000-67593600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
36	chr3:67587000-67620200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
37	chr3:67587400-67628000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
38	chr3:67588800-67602200	Weak transcription	Primary T helper cells fromperipheralblood	blood
39	chr3:67589000-67593600	Weak transcription	Primary T cells fromperipheralblood	blood
40	chr3:67589000-67603000	Weak transcription	Primary T helper cells PMA-I stimulated	--
41	chr3:67589800-67615000	Weak transcription	HSMMtube	muscle
42	chr3:67590000-67590400	Enhancers	Liver	Liver
43	chr3:67590200-67590600	Enhancers	HepG2	liver
44	chr3:67590400-67591600	Flanking Active TSS	Liver	Liver
45	chr3:67590600-67591000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
46	chr3:67590600-67591400	Enhancers	iPS-18 Cell Line	embryonic stem cell
47	chr3:67590600-67591400	Flanking Active TSS	HepG2	liver
48	chr3:67590800-67591200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
49	chr3:67590800-67591200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
50	chr3:67590800-67591200	ZNF genes & repeats	Fetal Stomach	stomach

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