Variant report

Variant	nsv3214
Chromosome Location	chr2:234384436-234416949
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:520)
CpG islands
(count:854)
Chromatin interactive
region (count:63)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:520 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF3	chr2:234395477-234396276	A549	lung:	n/a	n/a
2	ATF3	chr2:234395387-234396312	A549	lung:	n/a	n/a
3	BATF	chr2:234412951-234413156	GM12878	blood:	n/a	n/a
4	BATF	chr2:234409842-234410163	GM12878	blood:	n/a	n/a
5	BCL3	chr2:234395190-234397404	A549	lung:	n/a	n/a
6	BCL3	chr2:234394913-234396277	A549	lung:	n/a	n/a
7	CEBPB	chr2:234397004-234397393	IMR90	lung:	n/a	n/a
8	CEBPB	chr2:234391033-234391065	A549	lung:	n/a	n/a
9	CEBPB	chr2:234409398-234410196	IMR90	lung:	n/a	chr2:234409826-234409837
10	CEBPB	chr2:234412393-234412697	HepG2	liver:	n/a	n/a
11	CEBPB	chr2:234398387-234398761	Hela-S3	cervix:	n/a	chr2:234398572-234398585
12	CEBPB	chr2:234412388-234412660	IMR90	lung:	n/a	n/a
13	CEBPB	chr2:234398358-234398787	IMR90	lung:	n/a	chr2:234398572-234398585
14	CEBPB	chr2:234394268-234394496	HepG2	liver:	n/a	chr2:234394349-234394360 chr2:234394347-234394360 chr2:234394347-234394358
15	CEBPB	chr2:234395419-234396484	A549	lung:	n/a	n/a
16	CEBPB	chr2:234409792-234409899	HepG2	liver:	n/a	chr2:234409826-234409837
17	CEBPB	chr2:234395679-234396241	MCF-7	breast:	n/a	n/a
18	CEBPB	chr2:234398478-234398752	A549	lung:	n/a	chr2:234398572-234398585
19	CEBPB	chr2:234395558-234396220	Hela-S3	cervix:	n/a	n/a
20	CEBPB	chr2:234400879-234401079	A549	lung:	n/a	n/a
21	CEBPB	chr2:234395553-234396167	A549	lung:	n/a	n/a
22	CEBPB	chr2:234395580-234396182	A549	lung:	n/a	n/a
23	CEBPB	chr2:234412418-234412622	A549	lung:	n/a	n/a
24	CREB1	chr2:234388677-234388927	A549	lung:	n/a	n/a
25	CREB1	chr2:234395357-234395835	A549	lung:	n/a	n/a
26	CREB1	chr2:234395597-234396050	A549	lung:	n/a	n/a
27	CTCF	chr2:234389160-234389310	WERI-Rb-1	eye:	n/a	chr2:234389251-234389267
28	CTCF	chr2:234389160-234389310	HMF	breast:	n/a	chr2:234389251-234389267
29	CTCF	chr2:234389106-234389399	GM12878	blood:	n/a	chr2:234389251-234389267
30	CTCF	chr2:234389619-234389745	GM12878	blood:	n/a	chr2:234389664-234389677
31	CTCF	chr2:234406918-234407012	GM13977	blood:	n/a	n/a
32	CTCF	chr2:234389521-234389801	NHEK	skin:	n/a	chr2:234389664-234389677
33	CTCF	chr2:234406880-234407030	GM12873	blood:	n/a	n/a
34	CTCF	chr2:234389197-234389284	ProgFib	skin:	n/a	chr2:234389251-234389267
35	CTCF	chr2:234389160-234389310	HRE	kidney:	n/a	chr2:234389251-234389267
36	CTCF	chr2:234389236-234389357	IMR90	lung:	n/a	chr2:234389251-234389267
37	CTCF	chr2:234388720-234388870	Hela-S3	cervix:	n/a	n/a
38	CTCF	chr2:234388746-234388878	NHEK	skin:	n/a	n/a
39	CTCF	chr2:234389160-234389310	BE2_C	brain:	n/a	chr2:234389251-234389267
40	CTCF	chr2:234388720-234388870	GM12871	blood:	n/a	n/a
41	CTCF	chr2:234389680-234389830	RPTEC	kidney:	n/a	n/a
42	CTCF	chr2:234389180-234389330	RPTEC	kidney:	n/a	chr2:234389251-234389267
43	CTCF	chr2:234389080-234389230	HAc	cerebellar:	n/a	n/a
44	CTCF	chr2:234389160-234389310	HPF	lung:	n/a	chr2:234389251-234389267
45	CTCF	chr2:234389068-234389359	MCF-7	breast:	n/a	chr2:234389251-234389267
46	CTCF	chr2:234389644-234389716	GM19240	blood:	n/a	chr2:234389664-234389677
47	CTCF	chr2:234389120-234389270	HEEpiC	esophagus:	n/a	chr2:234389251-234389267
48	CTCF	chr2:234389200-234389350	HBMEC	blood vessel:	n/a	chr2:234389251-234389267
49	CTCF	chr2:234389520-234389670	HBMEC	blood vessel:	n/a	n/a
50	CTCF	chr2:234389600-234389750	HCPEpiC	choroid plexus:	n/a	chr2:234389664-234389677

(count:854 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:234386471-234386521	CMK	blood:	n/a
2	chr2:234394478-234394528	AoSMC	blood vessel:	n/a
3	chr2:234394645-234394695	BJ	skin:	n/a
4	chr2:234384677-234384727	Jurkat	blood:	n/a
5	chr2:234389140-234389190	CMK	blood:	n/a
6	chr2:234394478-234394528	T-47D	breast:	n/a
7	chr2:234389140-234389190	Jurkat	blood:	n/a
8	chr2:234389140-234389190	A549	lung:	n/a
9	chr2:234386471-234386521	ovcar-3	ovarian:	n/a
10	chr2:234395837-234395887	PFSK-1	brain:	n/a
11	chr2:234390545-234390595	K562	blood:	n/a
12	chr2:234384950-234385000	ECC-1	luminal epithelium:	n/a
13	chr2:234394478-234394528	SK-N-SH	brain:	n/a
14	chr2:234394645-234394695	K562	blood:	n/a
15	chr2:234384677-234384727	T-47D	breast:	n/a
16	chr2:234386471-234386521	SKMC	muscle:	n/a
17	chr2:234386471-234386521	HIPEpiC	eye:	n/a
18	chr2:234384950-234385000	SK-N-SH	brain:	n/a
19	chr2:234389140-234389190	HEK293	kidney:	embryo
20	chr2:234386652-234386702	U87	brain:	n/a
21	chr2:234385625-234385675	ECC-1	luminal epithelium:	n/a
22	chr2:234394541-234394591	HEEpiC	esophagus:	n/a
23	chr2:234389140-234389190	SKMC	muscle:	n/a
24	chr2:234394645-234394695	IMR90	lung:	fetal
25	chr2:234394645-234394695	AoSMC	blood vessel:	n/a
26	chr2:234389140-234389190	GM19239	blood:	n/a
27	chr2:234384950-234385000	HNPCEpiC	eye:	n/a
28	chr2:234384677-234384727	HRCEpiC	kidney:	n/a
29	chr2:234394645-234394695	H1-hESC	embryonic stem cell:	embryo
30	chr2:234394645-234394695	U87	brain:	n/a
31	chr2:234390545-234390595	HRE	kidney:	n/a
32	chr2:234386652-234386702	NHDF-neo	bronchial:	n/a
33	chr2:234384950-234385000	K562	blood:	n/a
34	chr2:234386471-234386521	Hela-S3	cervix:	n/a
35	chr2:234390545-234390595	SK-N-SH_RA	brain:	n/a
36	chr2:234385625-234385675	BJ	skin:	n/a
37	chr2:234385359-234385409	AG10803	skin:	n/a
38	chr2:234385359-234385409	LNCaP	prostate:	n/a
39	chr2:234386055-234386105	ProgFib	skin:	n/a
40	chr2:234384677-234384727	SK-N-SH	brain:	n/a
41	chr2:234389140-234389190	NT2-D1	testis:	n/a
42	chr2:234385502-234385552	HCF	heart:	n/a
43	chr2:234390545-234390595	RPTEC	kidney:	n/a
44	chr2:234385359-234385409	AoSMC	blood vessel:	n/a
45	chr2:234394541-234394591	K562	blood:	n/a
46	chr2:234394478-234394528	HCT-116	colon:	n/a
47	chr2:234385359-234385409	HEEpiC	esophagus:	n/a
48	chr2:234389140-234389190	HRE	kidney:	n/a
49	chr2:234386652-234386702	AG09309	skin:	n/a
50	chr2:234395837-234395887	BJ	skin:	n/a

(count:63 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr2:234356161..234358499-chr2:234388405..234391243,2	MCF-7	breast:
2	chr2:234388753..234400184-chr2:234596527..234603213,35	MCF-7	breast:
3	chr2:234390637..234392583-chr2:234428412..234431131,2	K562	blood:
4	chr2:234384920..234387471-chr2:234750794..234752642,2	MCF-7	breast:
5	chr2:234377292..234380088-chr2:234386184..234389025,2	MCF-7	breast:
6	chr2:234404504..234406876-chr2:234739242..234740869,2	MCF-7	breast:
7	chr2:234402660..234404605-chr2:234407982..234410172,3	MCF-7	breast:
8	chr2:234378675..234382523-chr2:234390792..234394362,4	K562	blood:
9	chr2:234394199..234396835-chr2:234450285..234452802,2	MCF-7	breast:
10	chr2:234393680..234401613-chr2:234597738..234605139,18	MCF-7	breast:
11	chr2:234386214..234389809-chr2:234395089..234397205,3	MCF-7	breast:
12	chr2:234386026..234387769-chr2:234390744..234392267,2	K562	blood:
13	chr2:234379094..234382048-chr2:234385373..234387118,2	K562	blood:
14	chr2:234388813..234389712-chr2:234741180..234742155,6	MCF-7	breast:
15	chr2:234382718..234385306-chr2:234606454..234608053,2	MCF-7	breast:
16	chr2:234395375..234398231-chr2:234399551..234402111,5	MCF-7	breast:
17	chr2:234389092..234391362-chr2:234473035..234476486,3	MCF-7	breast:
18	chr2:234386808..234389018-chr2:234473935..234476194,3	MCF-7	breast:
19	chr2:234372522..234374797-chr2:234385082..234387543,2	MCF-7	breast:
20	chr2:234385429..234386965-chr2:234599786..234601809,2	MCF-7	breast:
21	chr2:234405752..234408399-chr2:234409710..234413994,3	K562	blood:
22	chr2:234381434..234384275-chr2:234387365..234389292,3	K562	blood:
23	chr2:234388450..234390817-chr2:234616855..234619470,2	MCF-7	breast:
24	chr2:234385374..234387769-chr2:234390767..234392853,2	K562	blood:
25	chr2:234386214..234389809-chr2:234395089..234397205,3	MCF-7	breast:
26	chr2:234395274..234395960-chr2:234608595..234609417,2	MCF-7	breast:
27	chr2:234395612..234396510-chr2:234608589..234609593,3	MCF-7	breast:
28	chr2:234357885..234360671-chr2:234393955..234395750,2	MCF-7	breast:
29	chr2:234393460..234398388-chr2:234612624..234620814,16	MCF-7	breast:
30	chr2:234382281..234385759-chr2:234386993..234388960,3	MCF-7	breast:
31	chr2:234398690..234402106-chr2:234407622..234410683,3	MCF-7	breast:
32	chr2:234395319..234396920-chr2:234593778..234595799,2	MCF-7	breast:
33	chr2:234412826..234415197-chr2:234600328..234602184,2	MCF-7	breast:
34	chr2:234400113..234401794-chr2:234403565..234406076,3	MCF-7	breast:
35	chr2:234389181..234390135-chr2:234619766..234620786,6	MCF-7	breast:
36	chr2:234395630..234397717-chr2:234604680..234606573,2	MCF-7	breast:
37	chr2:234402660..234404605-chr2:234407982..234410172,3	MCF-7	breast:
38	chr2:234395375..234398231-chr2:234399551..234402111,5	MCF-7	breast:
39	chr2:234385784..234388460-chr2:234396665..234399378,2	MCF-7	breast:
40	chr2:234392329..234394453-chr2:234472244..234475115,2	MCF-7	breast:
41	chr2:234400872..234402381-chr2:234473582..234476254,2	MCF-7	breast:
42	chr2:234387239..234389851-chr2:234760888..234763623,2	MCF-7	breast:
43	chr2:234377261..234380113-chr2:234384331..234386065,2	MCF-7	breast:
44	chr2:234406540..234408040-chr2:234435707..234437772,2	K562	blood:
45	chr2:234400113..234401794-chr2:234403565..234406076,3	MCF-7	breast:
46	chr2:234389632..234392009-chr2:234393676..234396865,6	MCF-7	breast:
47	chr2:234377166..234379474-chr2:234382800..234384518,2	K562	blood:
48	chr2:234416542..234418917-chr2:234598476..234600704,2	MCF-7	breast:
49	chr2:234387565..234390486-chr2:234761608..234763193,2	MCF-7	breast:
50	chr2:234395688..234396257-chr2:234608075..234608944,2	MCF-7	breast:

No data

Variant related genes	Relation type
USP40	TF binding region
USP40	CpG island
ENSG00000167165	chromatin interactions
ENSG00000085982	chromatin interactions
ENSG00000077044	chromatin interactions
ENSG00000224814	chromatin interactions
ENSG00000123485	chromatin interactions

Extended variants
information (count: 1407 )
Associated
traits (count: 64 )

Variant overlapped rSNPs/rCNVs (count:1407 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs78905498	chr2:234384496-234384497	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs557201552	chr2:234384510-234384511	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs79513093	chr2:234384518-234384519	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs113330823	chr2:234384524-234384525	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs112101112	chr2:234384582-234384583	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs571852785	chr2:234384593-234384594	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs7724	chr2:234384596-234384597	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs531084911	chr2:234384609-234384610	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs537611422	chr2:234384610-234384611	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs189645204	chr2:234384637-234384638	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs563929732	chr2:234384654-234384655	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs577539192	chr2:234384682-234384683	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs543368394	chr2:234384683-234384684	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs563610134	chr2:234384691-234384692	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs111903797	chr2:234384692-234384693	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs9941591	chr2:234384698-234384699	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs373111998	chr2:234384705-234384706	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs180855488	chr2:234384728-234384729	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs368536892	chr2:234384729-234384730	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs7567008	chr2:234384750-234384751	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs138330169	chr2:234384754-234384755	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs537415781	chr2:234384766-234384767	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs550544564	chr2:234384789-234384790	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs117629299	chr2:234384791-234384792	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs114101228	chr2:234384851-234384852	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs186231861	chr2:234384852-234384853	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs573340286	chr2:234384871-234384872	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs557639786	chr2:234384876-234384877	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs534442436	chr2:234384898-234384899	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs111949296	chr2:234384904-234384905	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs577650588	chr2:234384907-234384908	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs543469274	chr2:234384908-234384909	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs563268740	chr2:234384915-234384916	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs191081573	chr2:234384957-234384958	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs75668778	chr2:234384963-234384964	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs73997612	chr2:234384978-234384979	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs144084353	chr2:234385005-234385006	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs543051047	chr2:234385008-234385009	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs544490360	chr2:234385059-234385060	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs565411215	chr2:234385089-234385090	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs80139629	chr2:234385111-234385112	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs551905142	chr2:234385142-234385143	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs550602176	chr2:234385145-234385146	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs567283302	chr2:234385149-234385150	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs573029681	chr2:234385164-234385165	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs375704351	chr2:234385176-234385177	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs78991956	chr2:234385177-234385178	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs565005915	chr2:234385182-234385183	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs371787454	chr2:234385246-234385247	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs530642117	chr2:234385253-234385254	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:64)

Disease	PMID	Source
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	21979893	CNVD
Ependymoma	16718352	CNVD
Melanoma	18172304	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	17603634	CNVD
Breast cancer	16272173	CNVD
Ewing''s sarcoma	17952124	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Autism	16446308	CNVD
Autism	19401682	CNVD
Colorectal cancer	16272173	CNVD
Lung cancer	18438408	CNVD
Acute myeloid leukemia	20729466	CNVD
small cell lung cancer	20016488	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
Urothelial carcinoma	21177765	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Cervical cancer	21062161	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Chordoma	18071362	CNVD
Developmental delay	21147756	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Cancer	22429812	CNVD
Bladder cancer	21909424	CNVD
Renal cell carcinoma	21668985	CNVD
Breast cancer	21785460	CNVD
Prostate cancer	18632612	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Wilms tumour	21544195	CNVD
Esophageal adenocarcinoma	18519675	CNVD
prenatal diagnosis	22389664	CNVD
Myelofibrosis	22110671	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Mental retardation	20152051	CNVD
Cancer	21183584	CNVD
Albright''s disease	22277900	CNVD
Brachydactyly-Mental Retardation Syndrome	22470819	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Colorectal cancer	19359472	CNVD
Autism	18414403	CNVD
Chronic myeloid leukemia	21384125	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Congenital anomalies of the kidney and urinary tract	20605837	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:1249 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:234339600-234394200	Weak transcription	HUVEC	blood vessel
2	chr2:234339800-234391400	Weak transcription	NHDF-Ad	bronchial
3	chr2:234343000-234393000	Strong transcription	Primary T cells from cord blood	blood
4	chr2:234343000-234402200	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
5	chr2:234361200-234389800	Weak transcription	Fetal Kidney	kidney
6	chr2:234362400-234384600	Strong transcription	Spleen	Spleen
7	chr2:234363800-234390600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
8	chr2:234364000-234411200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
9	chr2:234365800-234393600	Weak transcription	Hela-S3	cervix
10	chr2:234373000-234392200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
11	chr2:234373000-234409800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
12	chr2:234373400-234391000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
13	chr2:234373800-234404400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
14	chr2:234375200-234388000	Strong transcription	Lung	lung
15	chr2:234375400-234411200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
16	chr2:234375600-234387400	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
17	chr2:234376000-234389400	Weak transcription	NH-A	brain
18	chr2:234376200-234390200	Weak transcription	Pancreatic Islets	Pancreatic Islet
19	chr2:234377800-234385600	Weak transcription	Aorta	Aorta
20	chr2:234377800-234391400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
21	chr2:234377800-234397200	Weak transcription	Small Intestine	intestine
22	chr2:234378000-234387000	Weak transcription	HSMM	muscle
23	chr2:234378200-234395000	Weak transcription	Right Atrium	heart
24	chr2:234378400-234388000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
25	chr2:234378400-234390200	Weak transcription	HUES6 Cell Line	embryonic stem cell
26	chr2:234378400-234390800	Weak transcription	H9 Cell Line	embryonic stem cell
27	chr2:234378400-234391000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
28	chr2:234378600-234391600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
29	chr2:234378800-234384800	Weak transcription	Muscle Satellite Cultured Cells	--
30	chr2:234378800-234391400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
31	chr2:234379000-234386600	Weak transcription	HepG2	liver
32	chr2:234379000-234391200	Weak transcription	HUES48 Cell Line	embryonic stem cell
33	chr2:234379400-234384600	Weak transcription	Brain Germinal Matrix	brain
34	chr2:234379400-234384600	Weak transcription	Fetal Lung	lung
35	chr2:234379400-234388400	Weak transcription	Stomach Mucosa	stomach
36	chr2:234379600-234386400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
37	chr2:234379800-234384800	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
38	chr2:234380200-234384600	Weak transcription	Psoas Muscle	Psoas
39	chr2:234380200-234384600	Weak transcription	Dnd41	blood
40	chr2:234380400-234390200	Weak transcription	HMEC	breast
41	chr2:234380800-234386000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
42	chr2:234380800-234395000	Strong transcription	Foreskin Fibroblast Primary Cells skin02	Skin
43	chr2:234381000-234384600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
44	chr2:234381200-234394800	Strong transcription	Pancreas	Pancrea
45	chr2:234381400-234384600	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
46	chr2:234381400-234389000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
47	chr2:234381600-234384600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
48	chr2:234381600-234385200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
49	chr2:234381600-234391000	Weak transcription	Primary T helper cells PMA-I stimulated	--
50	chr2:234381600-234393400	Weak transcription	Primary hematopoietic stem cells	blood

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