Variant report

Variant	nsv540623
Chromosome Location	chr10:49805087-49819765
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:416)
CpG islands
(count:1161)
Chromatin interactive
region (count:22)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:416 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr10:49811814-49811882	K562	blood:	n/a	n/a
2	BACH1	chr10:49812923-49813113	H1-hESC	embryonic stem cell:	n/a	n/a
3	BATF	chr10:49817447-49817735	GM12878	blood:	n/a	chr10:49817613-49817624
4	BHLHE40	chr10:49816207-49816497	K562	blood:	n/a	n/a
5	BHLHE40	chr10:49814656-49814773	K562	blood:	n/a	n/a
6	CEBPB	chr10:49815028-49815209	HepG2	liver:	n/a	n/a
7	CEBPB	chr10:49814986-49815341	Hela-S3	cervix:	n/a	n/a
8	CEBPB	chr10:49810472-49810745	IMR90	lung:	n/a	n/a
9	CEBPB	chr10:49814650-49815462	IMR90	lung:	n/a	n/a
10	CEBPB	chr10:49814966-49815229	K562	blood:	n/a	n/a
11	CEBPB	chr10:49814976-49815261	MCF-7	breast:	n/a	n/a
12	CEBPB	chr10:49814997-49815192	K562	blood:	n/a	n/a
13	CEBPB	chr10:49815003-49815291	A549	lung:	n/a	n/a
14	CEBPB	chr10:49814997-49815283	K562	blood:	n/a	n/a
15	CTCF	chr10:49816240-49816390	HA-sp	spinal cord:	n/a	n/a
16	CTCF	chr10:49816280-49816430	HFF-Myc	foreskin:	n/a	n/a
17	CTCF	chr10:49816259-49816492	HepG2	liver:	n/a	n/a
18	CTCF	chr10:49815997-49816074	GM19238	blood:	n/a	n/a
19	CTCF	chr10:49816320-49816470	K562	blood:	n/a	n/a
20	CTCF	chr10:49816300-49816450	Caco-2	colon:	n/a	n/a
21	CTCF	chr10:49816340-49816490	GM12865	blood:	n/a	n/a
22	CTCF	chr10:49816667-49816728	K562	blood:	n/a	n/a
23	CTCF	chr10:49816300-49816450	HEEpiC	esophagus:	n/a	n/a
24	CTCF	chr10:49816280-49816430	NHLF	lung:	n/a	n/a
25	CTCF	chr10:49816280-49816430	HMEC	breast:	n/a	n/a
26	CTCF	chr10:49816219-49816529	GM12891	blood:	n/a	n/a
27	CTCF	chr10:49816340-49816490	HFF-Myc	foreskin:	n/a	n/a
28	CTCF	chr10:49816610-49816742	GM19240	blood:	n/a	n/a
29	CTCF	chr10:49816200-49816350	HFF	foreskin:	n/a	n/a
30	CTCF	chr10:49816300-49816450	SAEC	small airway:	n/a	n/a
31	CTCF	chr10:49816300-49816450	BE2_C	brain:	n/a	n/a
32	CTCF	chr10:49815860-49816010	HBMEC	blood vessel:	n/a	n/a
33	CTCF	chr10:49815140-49815290	HCPEpiC	choroid plexus:	n/a	n/a
34	CTCF	chr10:49816130-49816547	K562	blood:	n/a	n/a
35	CTCF	chr10:49815680-49815830	HMF	breast:	n/a	n/a
36	CTCF	chr10:49816280-49816430	NB4	blood:	n/a	n/a
37	CTCF	chr10:49816280-49816430	GM12864	blood:	n/a	n/a
38	CTCF	chr10:49816620-49816770	GM12866	blood:	n/a	n/a
39	CTCF	chr10:49816280-49816430	RPTEC	kidney:	n/a	n/a
40	CTCF	chr10:49816162-49816484	ECC-1	luminal epithelium:	n/a	n/a
41	CTCF	chr10:49816261-49816432	A549	lung:	n/a	n/a
42	CTCF	chr10:49816320-49816470	HRE	kidney:	n/a	n/a
43	CTCF	chr10:49815600-49815750	GM12874	blood:	n/a	n/a
44	CTCF	chr10:49814840-49814990	K562	blood:	n/a	n/a
45	CTCF	chr10:49816093-49816101	GM12878	blood:	n/a	n/a
46	CTCF	chr10:49816251-49816471	GM13976	blood:	n/a	n/a
47	CTCF	chr10:49816280-49816430	Caco-2	colon:	n/a	n/a
48	CTCF	chr10:49815380-49815530	HBMEC	blood vessel:	n/a	n/a
49	CTCF	chr10:49816320-49816470	AoAF	blood vessel:	n/a	n/a
50	CTCF	chr10:49815740-49815890	AG04449	skin:	n/a	n/a

(count:1161 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:49812686-49812736	HCPEpiC	choroid plexus:	n/a
2	chr10:49813128-49813178	Hela-S3	cervix:	n/a
3	chr10:49812686-49812736	HCPEpiC	choroid plexus:	n/a
4	chr10:49813128-49813178	Hela-S3	cervix:	n/a
5	chr10:49812867-49812917	PFSK-1	brain:	n/a
6	chr10:49813307-49813357	NB4	blood:	n/a
7	chr10:49815243-49815293	T-47D	breast:	n/a
8	chr10:49812963-49813013	GM12892	blood:	n/a
9	chr10:49812258-49812308	GM12892	blood:	n/a
10	chr10:49815243-49815293	MCF-7	breast:	n/a
11	chr10:49807993-49808043	HRCEpiC	kidney:	n/a
12	chr10:49815243-49815293	HUVEC	blood vessel:	n/a
13	chr10:49812867-49812917	HRE	kidney:	n/a
14	chr10:49813142-49813192	PANC-1	pancreas:	n/a
15	chr10:49813265-49813315	HRCEpiC	kidney:	n/a
16	chr10:49813208-49813258	PFSK-1	brain:	n/a
17	chr10:49812258-49812308	HNPCEpiC	eye:	n/a
18	chr10:49816684-49816734	T-47D	breast:	n/a
19	chr10:49812867-49812917	BJ	skin:	n/a
20	chr10:49812963-49813013	MCF-7	breast:	n/a
21	chr10:49813128-49813178	Hepatocyte	liver:	n/a
22	chr10:49812867-49812917	HMEC	breast:	n/a
23	chr10:49815243-49815293	HRPEpiC	eye:	n/a
24	chr10:49816684-49816734	SAEC	small airway:	n/a
25	chr10:49810606-49810656	HNPCEpiC	eye:	n/a
26	chr10:49810606-49810656	ECC-1	luminal epithelium:	n/a
27	chr10:49813128-49813178	BE2_C	brain:	n/a
28	chr10:49813142-49813192	AoSMC	blood vessel:	n/a
29	chr10:49813307-49813357	NHBE	bronchial:	n/a
30	chr10:49813371-49813421	MCF-7	breast:	n/a
31	chr10:49813142-49813192	HCPEpiC	choroid plexus:	n/a
32	chr10:49807993-49808043	SK-N-SH_RA	brain:	n/a
33	chr10:49813208-49813258	HEEpiC	esophagus:	n/a
34	chr10:49813434-49813484	HUVEC	blood vessel:	n/a
35	chr10:49813208-49813258	H1-hESC	embryonic stem cell:	embryo
36	chr10:49812686-49812736	HUVEC	blood vessel:	n/a
37	chr10:49813208-49813258	U87	brain:	n/a
38	chr10:49813142-49813192	HRE	kidney:	n/a
39	chr10:49815243-49815293	NHDF-neo	bronchial:	n/a
40	chr10:49811797-49811847	K562	blood:	n/a
41	chr10:49812686-49812736	PFSK-1	brain:	n/a
42	chr10:49813434-49813484	SK-N-SH_RA	brain:	n/a
43	chr10:49812258-49812308	SK-N-SH_RA	brain:	n/a
44	chr10:49813371-49813421	IMR90	lung:	fetal
45	chr10:49813296-49813346	HUVEC	blood vessel:	n/a
46	chr10:49810606-49810656	SK-N-MC	brain:	n/a
47	chr10:49813128-49813178	NHDF-neo	bronchial:	n/a
48	chr10:49813128-49813178	NH-A	brain:	n/a
49	chr10:49813265-49813315	SK-N-SH	brain:	n/a
50	chr10:49813128-49813178	ProgFib	skin:	n/a

(count:22 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr10:49812643..49815279-chr10:49817934..49821454,3	K562	blood:
2	chr10:49815968..49816808-chr10:49864279..49864833,3	K562	blood:
3	chr10:49815968..49816895-chr10:49863852..49864729,3	MCF-7	breast:
4	chr10:49807954..49810165-chr10:49813805..49816263,2	K562	blood:
5	chr10:49807563..49809582-chr10:49811052..49813456,2	K562	blood:
6	chr10:49814889..49815804-chr10:49864121..49864723,2	MCF-7	breast:
7	chr10:49815515..49817850-chr10:49821567..49823368,2	K562	blood:
8	chr10:49814646..49816346-chr10:49859751..49862442,2	MCF-7	breast:
9	chr10:49803449..49806328-chr10:49810436..49812286,2	K562	blood:
10	chr10:49816362..49818003-chr10:49818843..49820950,2	K562	blood:
11	chr10:49815980..49816521-chr5:30063610..30064465,2	MCF-7	breast:
12	chr10:49698335..49701028-chr10:49818067..49819689,2	K562	blood:
13	chr10:49759598..49760543-chr10:49815964..49816843,2	MCF-7	breast:
14	chr10:49816362..49818003-chr10:49818843..49820950,2	K562	blood:
15	chr10:49804967..49805487-chr18:43382414..43383035,2	MCF-7	breast:
16	chr10:49815976..49817103-chr10:49863928..49864923,9	MCF-7	breast:
17	chr10:49804878..49807273-chr10:49811904..49814201,2	MCF-7	breast:
18	chr10:49784932..49786991-chr10:49803496..49805915,2	K562	blood:
19	chr10:49814485..49816162-chr10:49819695..49822517,2	MCF-7	breast:
20	chr10:49807954..49810165-chr10:49813805..49816263,2	K562	blood:
21	chr10:49814485..49816162-chr10:49819695..49822517,2	MCF-7	breast:
22	chr10:49803449..49806328-chr10:49810436..49812286,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-WDFY4-2	chr10:49812817-49813142	ENSG00000250000

No data

Variant related genes	Relation type
ARHGAP22	TF binding region
ARHGAP22	CpG island
ENSG00000128805	chromatin interactions
GSK3B	miRNA target sites

Extended variants
information (count: 569 )
Associated
traits (count: 71 )

Variant overlapped rSNPs/rCNVs (count:569 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs372633880	chr10:49805089-49805090	Weak transcription Genic enhancers Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs571906269	chr10:49805105-49805106	Weak transcription Genic enhancers Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs140113383	chr10:49805127-49805128	Weak transcription Genic enhancers Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs191654540	chr10:49805145-49805146	Weak transcription Genic enhancers Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs568399955	chr10:49805148-49805149	Weak transcription Genic enhancers Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs79351541	chr10:49805177-49805178	Weak transcription Genic enhancers Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs111425347	chr10:49805192-49805193	Weak transcription Genic enhancers Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs186477340	chr10:49805197-49805198	Weak transcription Genic enhancers Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs11101394	chr10:49805216-49805217	Weak transcription Enhancers Genic enhancers Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs150303952	chr10:49805235-49805236	Weak transcription Enhancers Genic enhancers Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs137887068	chr10:49805255-49805256	Weak transcription Enhancers Genic enhancers Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs111333231	chr10:49805304-49805305	Weak transcription Enhancers Genic enhancers Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs10776628	chr10:49805368-49805369	Weak transcription Enhancers Genic enhancers Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs113918162	chr10:49805426-49805427	Weak transcription Enhancers Genic enhancers Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs11101395	chr10:49805511-49805512	Weak transcription Enhancers Genic enhancers Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs11101396	chr10:49805553-49805554	Weak transcription Enhancers Genic enhancers Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs376401175	chr10:49805556-49805557	Weak transcription Enhancers Genic enhancers Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs540680942	chr10:49805565-49805566	Weak transcription Enhancers Genic enhancers Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs369961337	chr10:49805567-49805568	Weak transcription Enhancers Genic enhancers Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs12246089	chr10:49805575-49805576	Weak transcription Enhancers Genic enhancers Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs142701364	chr10:49805598-49805599	Weak transcription Enhancers Genic enhancers Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs17010927	chr10:49805605-49805606	Weak transcription Genic enhancers Strong transcription Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs550412878	chr10:49805657-49805658	Weak transcription Genic enhancers Strong transcription Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs146029067	chr10:49805664-49805665	Weak transcription Genic enhancers Strong transcription Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs7915604	chr10:49805670-49805671	Weak transcription Genic enhancers Strong transcription Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs547457410	chr10:49805682-49805683	Weak transcription Genic enhancers Strong transcription Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs566118197	chr10:49805684-49805685	Weak transcription Genic enhancers Strong transcription Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs79682764	chr10:49805694-49805695	Weak transcription Genic enhancers Strong transcription Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs185425624	chr10:49805703-49805704	Weak transcription Genic enhancers Strong transcription Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs190726977	chr10:49805723-49805724	Weak transcription Genic enhancers Strong transcription Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs544093174	chr10:49805754-49805755	Weak transcription Genic enhancers Strong transcription Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs536872453	chr10:49805766-49805767	Weak transcription Genic enhancers Strong transcription Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs4838631	chr10:49805799-49805800	Weak transcription Genic enhancers Strong transcription Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs193129044	chr10:49805814-49805815	Weak transcription Genic enhancers Strong transcription Transcr. at gene 5' and 3' Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs115765943	chr10:49805873-49805874	Weak transcription Genic enhancers Strong transcription Transcr. at gene 5' and 3' Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs35127054	chr10:49805902-49805903	Weak transcription Genic enhancers Strong transcription Transcr. at gene 5' and 3' Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs552548368	chr10:49805920-49805921	Weak transcription Genic enhancers Strong transcription Transcr. at gene 5' and 3' Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs185223342	chr10:49805957-49805958	Weak transcription Genic enhancers Strong transcription Transcr. at gene 5' and 3' Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs544661720	chr10:49805990-49805991	Weak transcription Genic enhancers Strong transcription Transcr. at gene 5' and 3' Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs563056970	chr10:49806010-49806011	Weak transcription Enhancers Genic enhancers Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs576548684	chr10:49806017-49806018	Weak transcription Enhancers Genic enhancers Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs189231264	chr10:49806052-49806053	Weak transcription Enhancers Genic enhancers Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs181268988	chr10:49806105-49806106	Weak transcription Enhancers Genic enhancers Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs536777965	chr10:49806107-49806108	Weak transcription Enhancers Genic enhancers Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs548155270	chr10:49806112-49806113	Weak transcription Enhancers Genic enhancers Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs542484533	chr10:49806162-49806163	Weak transcription Enhancers Genic enhancers Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs11101397	chr10:49806169-49806170	Weak transcription Enhancers Genic enhancers Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs533381117	chr10:49806212-49806213	Weak transcription Enhancers Genic enhancers Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs7916314	chr10:49806232-49806233	Weak transcription Enhancers Genic enhancers Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs11101398	chr10:49806242-49806243	Weak transcription Enhancers Genic enhancers Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:71)

Disease	PMID	Source
Pancreatic endocrine tumor	17639061	CNVD
Gastric cancer	17908304	CNVD
Chordoma	21602918	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	21979893	CNVD
Melanoma	18172304	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Ewing''s sarcoma	17952124	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	20724749	CNVD
Autism	22495311	CNVD
Esophageal cancer	21851588	CNVD
Prostate cancer	18632612	CNVD
Autism	18414403	CNVD
Cockayne syndrome	18421352	CNVD
Glioblastoma	16823260	CNVD
Medulloblastoma	16968546	CNVD
Neuroblastoma	17533364	CNVD
Cancer	21183584	CNVD
T-cell lymphomas	19863542	CNVD
Testicular germ cell tumor	18059402	CNVD
Squamous cell cancer	21044232	CNVD
Glioma	21971842	CNVD
Cancer	21637783	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Colorectal cancer	20709793	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Papillary thyroid carcinoma	21436994	CNVD
Hirschsprung''s Disease	21712996	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Obesity	21956041	CNVD
Renal cell carcinoma	18765545	CNVD
Developmental delay	21948486	CNVD
Dysmorphic features	21948486	CNVD
Epilepsy	21948486	CNVD
Breast cancer	21785460	CNVD
Intellectual disability	21948486	CNVD
Schizophrenia	23813976	CNVD
Acute myeloid leukemia	19651601	CNVD
Breast cancer	20409316	CNVD
Breast cancer	21990379	CNVD
Myelofibrosis	22110671	CNVD
Rett syndrome	21593744	CNVD
Glioblastoma multiforme	22286061	CNVD
Neuroblastoma	21899760	CNVD
Intellectual disability	22045946	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Autism	21948486	CNVD
cleft palate	21948486	CNVD
Encephalopathy	21948486	CNVD
Lung cancer	18438408	CNVD
T-cell primary immunodeficiency	21948486	CNVD
Autism	22543975	CNVD
Breast cancer	21364760	CNVD
Developmental delay	21147756	CNVD
small cell lung cancer	20016488	CNVD
skeletal anomalies	21948486	CNVD
speech delay	21948486	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:616 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:49794400-49810600	Enhancers	Brain Substantia Nigra	brain
2	chr10:49797400-49812200	Weak transcription	Right Atrium	heart
3	chr10:49798600-49805600	Weak transcription	HSMMtube	muscle
4	chr10:49798800-49806000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
5	chr10:49798800-49806800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
6	chr10:49798800-49808200	Weak transcription	HMEC	breast
7	chr10:49799400-49808000	Weak transcription	HUVEC	blood vessel
8	chr10:49799400-49808800	Weak transcription	NH-A	brain
9	chr10:49800600-49809400	Enhancers	Brain Inferior Temporal Lobe	brain
10	chr10:49800800-49807800	Weak transcription	Ovary	ovary
11	chr10:49803000-49807400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
12	chr10:49803400-49807400	Strong transcription	Osteobl	bone
13	chr10:49803600-49805200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
14	chr10:49803800-49809600	Transcr. at gene 5' and 3'	Foreskin Fibroblast Primary Cells skin01	Skin
15	chr10:49804000-49807800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
16	chr10:49804000-49808400	Genic enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
17	chr10:49804200-49807000	Strong transcription	NHLF	lung
18	chr10:49804200-49807400	Genic enhancers	HSMM	muscle
19	chr10:49804200-49809600	Enhancers	Brain Hippocampus Middle	brain
20	chr10:49804400-49810800	Weak transcription	Gastric	stomach
21	chr10:49804600-49809200	Enhancers	Brain Anterior Caudate	brain
22	chr10:49804800-49805200	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
23	chr10:49804800-49805200	Transcr. at gene 5' and 3'	Foreskin Fibroblast Primary Cells skin02	Skin
24	chr10:49804800-49805400	Genic enhancers	NHDF-Ad	bronchial
25	chr10:49804800-49806200	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
26	chr10:49804800-49806400	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
27	chr10:49804800-49807600	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
28	chr10:49804800-49808200	Genic enhancers	Muscle Satellite Cultured Cells	--
29	chr10:49804800-49809200	Genic enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
30	chr10:49804800-49809400	Enhancers	Brain Cingulate Gyrus	brain
31	chr10:49805000-49806600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
32	chr10:49805000-49807400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
33	chr10:49805000-49809200	Enhancers	Brain Angular Gyrus	brain
34	chr10:49805200-49805600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
35	chr10:49805200-49805600	Genic enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
36	chr10:49805400-49806000	Weak transcription	NHDF-Ad	bronchial
37	chr10:49805600-49805800	Transcr. at gene 5' and 3'	Foreskin Fibroblast Primary Cells skin02	Skin
38	chr10:49805600-49807000	Enhancers	HSMMtube	muscle
39	chr10:49805600-49811000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
40	chr10:49805800-49806200	Genic enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
41	chr10:49805800-49806200	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
42	chr10:49806000-49806800	Enhancers	Fetal Muscle Leg	muscle
43	chr10:49806000-49807000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
44	chr10:49806000-49807000	Bivalent Enhancer	Fetal Muscle Trunk	muscle
45	chr10:49806000-49810000	Enhancers	NHDF-Ad	bronchial
46	chr10:49806200-49808800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
47	chr10:49806200-49809400	Transcr. at gene 5' and 3'	Foreskin Fibroblast Primary Cells skin02	Skin
48	chr10:49806400-49806800	Bivalent Enhancer	Ganglion Eminence derived primary cultured neurospheres	brain
49	chr10:49806400-49807600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
50	chr10:49806600-49808000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell

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