Variant report

Variant	nsv912591
Chromosome Location	chr20:1283523-1296811
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr20:1284914-1285109	K562	blood:	n/a	n/a
2	ATF3	chr20:1289968-1290275	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr20:1294067-1294472	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr20:1289999-1290199	H1-hESC	embryonic stem cell:	n/a	n/a
5	BHLHE40	chr20:1294180-1294466	GM12878	blood:	n/a	n/a
6	BHLHE40	chr20:1285433-1285717	K562	blood:	n/a	n/a
7	BHLHE40	chr20:1294195-1294496	K562	blood:	n/a	n/a
8	BRCA1	chr20:1294333-1294360	GM12878	blood:	n/a	n/a
9	BRCA1	chr20:1294316-1294516	HepG2	liver:	n/a	n/a
10	CEBPB	chr20:1294202-1294446	H1-hESC	embryonic stem cell:	n/a	n/a
11	CHD1	chr20:1294284-1294436	H1-hESC	embryonic stem cell:	n/a	n/a
12	CHD1	chr20:1294308-1294363	GM12878	blood:	n/a	n/a
13	CHD2	chr20:1294131-1294336	Hela-S3	cervix:	n/a	n/a
14	CHD2	chr20:1291122-1291228	HepG2	liver:	n/a	n/a
15	CHD2	chr20:1290127-1290213	H1-hESC	embryonic stem cell:	n/a	n/a
16	CHD2	chr20:1294106-1294254	HepG2	liver:	n/a	n/a
17	CHD2	chr20:1294008-1294452	H1-hESC	embryonic stem cell:	n/a	n/a
18	CTCF	chr20:1294240-1294390	HL-60	blood:	n/a	chr20:1294318-1294328 chr20:1294315-1294336 chr20:1294314-1294330 chr20:1294316-1294325 chr20:1294313-1294331
19	CTCF	chr20:1294220-1294370	AG04450	lung:	n/a	chr20:1294318-1294328 chr20:1294315-1294336 chr20:1294314-1294330 chr20:1294316-1294325 chr20:1294313-1294331
20	CTCF	chr20:1294000-1294584	K562	blood:	n/a	chr20:1294318-1294328 chr20:1294149-1294162 chr20:1294315-1294336 chr20:1294151-1294161 chr20:1294314-1294330 chr20:1294146-1294164 chr20:1294316-1294325 chr20:1294313-1294331
21	CTCF	chr20:1294136-1294445	GM19239	blood:	n/a	chr20:1294318-1294328 chr20:1294149-1294162 chr20:1294315-1294336 chr20:1294151-1294161 chr20:1294314-1294330 chr20:1294146-1294164 chr20:1294316-1294325 chr20:1294313-1294331
22	CTCF	chr20:1290080-1290230	WERI-Rb-1	eye:	n/a	chr20:1290141-1290162 chr20:1290146-1290164
23	CTCF	chr20:1294260-1294410	HPF	lung:	n/a	chr20:1294318-1294328 chr20:1294315-1294336 chr20:1294314-1294330 chr20:1294316-1294325 chr20:1294313-1294331
24	CTCF	chr20:1294240-1294390	GM12874	blood:	n/a	chr20:1294318-1294328 chr20:1294315-1294336 chr20:1294314-1294330 chr20:1294316-1294325 chr20:1294313-1294331
25	CTCF	chr20:1294073-1294527	Spleen_OC	spleen:	n/a	chr20:1294318-1294328 chr20:1294149-1294162 chr20:1294315-1294336 chr20:1294151-1294161 chr20:1294314-1294330 chr20:1294146-1294164 chr20:1294316-1294325 chr20:1294313-1294331
26	CTCF	chr20:1294260-1294410	AG09309	skin:	n/a	chr20:1294318-1294328 chr20:1294315-1294336 chr20:1294314-1294330 chr20:1294316-1294325 chr20:1294313-1294331
27	CTCF	chr20:1293540-1293690	GM12866	blood:	n/a	n/a
28	CTCF	chr20:1293979-1294462	GM19240	blood:	n/a	chr20:1294318-1294328 chr20:1294149-1294162 chr20:1294315-1294336 chr20:1294151-1294161 chr20:1294314-1294330 chr20:1294146-1294164 chr20:1294316-1294325 chr20:1294313-1294331
29	CTCF	chr20:1293964-1294457	GM12892	blood:	n/a	chr20:1294318-1294328 chr20:1294149-1294162 chr20:1294315-1294336 chr20:1294151-1294161 chr20:1294314-1294330 chr20:1294146-1294164 chr20:1294316-1294325 chr20:1294313-1294331
30	CTCF	chr20:1293998-1294436	MCF-7	breast:	n/a	chr20:1294318-1294328 chr20:1294149-1294162 chr20:1294315-1294336 chr20:1294151-1294161 chr20:1294314-1294330 chr20:1294146-1294164 chr20:1294316-1294325 chr20:1294313-1294331
31	CTCF	chr20:1294182-1294451	HUVEC	blood vessel:	n/a	chr20:1294318-1294328 chr20:1294315-1294336 chr20:1294314-1294330 chr20:1294316-1294325 chr20:1294313-1294331
32	CTCF	chr20:1294220-1294370	GM12869	blood:	n/a	chr20:1294318-1294328 chr20:1294315-1294336 chr20:1294314-1294330 chr20:1294316-1294325 chr20:1294313-1294331
33	CTCF	chr20:1294260-1294410	HBMEC	blood vessel:	n/a	chr20:1294318-1294328 chr20:1294315-1294336 chr20:1294314-1294330 chr20:1294316-1294325 chr20:1294313-1294331
34	CTCF	chr20:1294260-1294410	A549	lung:	n/a	chr20:1294318-1294328 chr20:1294315-1294336 chr20:1294314-1294330 chr20:1294316-1294325 chr20:1294313-1294331
35	CTCF	chr20:1294240-1294390	Hela-S3	cervix:	n/a	chr20:1294318-1294328 chr20:1294315-1294336 chr20:1294314-1294330 chr20:1294316-1294325 chr20:1294313-1294331
36	CTCF	chr20:1290116-1290225	Fibrobl	skin:	n/a	chr20:1290141-1290162 chr20:1290146-1290164
37	CTCF	chr20:1294159-1294452	MCF-7	breast:	n/a	chr20:1294318-1294328 chr20:1294315-1294336 chr20:1294314-1294330 chr20:1294316-1294325 chr20:1294313-1294331
38	CTCF	chr20:1294260-1294410	GM12865	blood:	n/a	chr20:1294318-1294328 chr20:1294315-1294336 chr20:1294314-1294330 chr20:1294316-1294325 chr20:1294313-1294331
39	CTCF	chr20:1290180-1290330	HRE	kidney:	n/a	n/a
40	CTCF	chr20:1294240-1294390	HRE	kidney:	n/a	chr20:1294318-1294328 chr20:1294315-1294336 chr20:1294314-1294330 chr20:1294316-1294325 chr20:1294313-1294331
41	CTCF	chr20:1294240-1294390	NHDF-neo	bronchial:	n/a	chr20:1294318-1294328 chr20:1294315-1294336 chr20:1294314-1294330 chr20:1294316-1294325 chr20:1294313-1294331
42	CTCF	chr20:1294240-1294390	HEEpiC	esophagus:	n/a	chr20:1294318-1294328 chr20:1294315-1294336 chr20:1294314-1294330 chr20:1294316-1294325 chr20:1294313-1294331
43	CTCF	chr20:1285440-1285590	K562	blood:	n/a	n/a
44	CTCF	chr20:1294260-1294410	GM12873	blood:	n/a	chr20:1294318-1294328 chr20:1294315-1294336 chr20:1294314-1294330 chr20:1294316-1294325 chr20:1294313-1294331
45	CTCF	chr20:1294220-1294370	GM12868	blood:	n/a	chr20:1294318-1294328 chr20:1294315-1294336 chr20:1294314-1294330 chr20:1294316-1294325 chr20:1294313-1294331
46	CTCF	chr20:1294178-1294439	Hela-S3	cervix:	n/a	chr20:1294318-1294328 chr20:1294315-1294336 chr20:1294314-1294330 chr20:1294316-1294325 chr20:1294313-1294331
47	CTCF	chr20:1294240-1294390	K562	blood:	n/a	chr20:1294318-1294328 chr20:1294315-1294336 chr20:1294314-1294330 chr20:1294316-1294325 chr20:1294313-1294331
48	CTCF	chr20:1294187-1294436	LNCaP	prostate:	n/a	chr20:1294318-1294328 chr20:1294315-1294336 chr20:1294314-1294330 chr20:1294316-1294325 chr20:1294313-1294331
49	CTCF	chr20:1293972-1294439	MCF-7	breast:	n/a	chr20:1294318-1294328 chr20:1294149-1294162 chr20:1294315-1294336 chr20:1294151-1294161 chr20:1294314-1294330 chr20:1294146-1294164 chr20:1294316-1294325 chr20:1294313-1294331
50	CTCF	chr20:1294016-1294508	H1-hESC	embryonic stem cell:	n/a	chr20:1294318-1294328 chr20:1294149-1294162 chr20:1294315-1294336 chr20:1294151-1294161 chr20:1294314-1294330 chr20:1294146-1294164 chr20:1294316-1294325 chr20:1294313-1294331

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr20:1294858-1294908	RPTEC	kidney:	n/a
2	chr20:1294858-1294908	RPTEC	kidney:	n/a
3	chr20:1289571-1289621	RPTEC	kidney:	n/a
4	chr20:1294311-1294361	HL-60	blood:	n/a
5	chr20:1294313-1294363	AG04450	lung:	fetal
6	chr20:1294301-1294351	NB4	blood:	n/a
7	chr20:1293560-1293610	GM12892	blood:	n/a
8	chr20:1285816-1285866	NB4	blood:	n/a
9	chr20:1294376-1294426	MCF10A-Er-Src	breast:	n/a
10	chr20:1285816-1285866	HCT-116	colon:	n/a
11	chr20:1289571-1289621	GM12878	blood:	n/a
12	chr20:1293560-1293610	HIPEpiC	eye:	n/a
13	chr20:1286630-1286680	NHBE	bronchial:	n/a
14	chr20:1286630-1286680	AG09309	skin:	n/a
15	chr20:1289571-1289621	K562	blood:	n/a
16	chr20:1294311-1294361	NHDF-neo	bronchial:	n/a
17	chr20:1294376-1294426	HL-60	blood:	n/a
18	chr20:1294361-1294411	AoSMC	blood vessel:	n/a
19	chr20:1286630-1286680	HEEpiC	esophagus:	n/a
20	chr20:1293560-1293610	MCF10A-Er-Src	breast:	n/a
21	chr20:1294311-1294361	IMR90	lung:	fetal
22	chr20:1287050-1287100	MCF10A-Er-Src	breast:	n/a
23	chr20:1286558-1286608	SK-N-SH_RA	brain:	n/a
24	chr20:1287050-1287100	CMK	blood:	n/a
25	chr20:1286558-1286608	NB4	blood:	n/a
26	chr20:1286558-1286608	BE2_C	brain:	n/a
27	chr20:1293560-1293610	GM12878	blood:	n/a
28	chr20:1293560-1293610	U87	brain:	n/a
29	chr20:1294311-1294361	MCF10A-Er-Src	breast:	n/a
30	chr20:1293682-1293732	PANC-1	pancreas:	n/a
31	chr20:1289571-1289621	ECC-1	luminal epithelium:	n/a
32	chr20:1289571-1289621	HRCEpiC	kidney:	n/a
33	chr20:1293682-1293732	NT2-D1	testis:	n/a
34	chr20:1294311-1294361	A549	lung:	n/a
35	chr20:1286558-1286608	Hela-S3	cervix:	n/a
36	chr20:1286558-1286608	GM12892	blood:	n/a
37	chr20:1294311-1294361	CMK	blood:	n/a
38	chr20:1294311-1294361	H1-hESC	embryonic stem cell:	embryo
39	chr20:1294021-1294071	HRCEpiC	kidney:	n/a
40	chr20:1286630-1286680	NH-A	brain:	n/a
41	chr20:1290724-1290774	SK-N-SH_RA	brain:	n/a
42	chr20:1294814-1294864	GM19239	blood:	n/a
43	chr20:1289571-1289621	BJ	skin:	n/a
44	chr20:1293560-1293610	ProgFib	skin:	n/a
45	chr20:1285816-1285866	Jurkat	blood:	n/a
46	chr20:1294021-1294071	NH-A	brain:	n/a
47	chr20:1294376-1294426	AG04449	skin:	fetal
48	chr20:1294376-1294426	GM19239	blood:	n/a
49	chr20:1293560-1293610	HRE	kidney:	n/a
50	chr20:1285816-1285866	GM19239	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr20:1292210..1295153-chr20:1372716..1374404,2	MCF-7	breast:
2	chr20:1296607..1299079-chr20:1367748..1369670,2	K562	blood:
3	chr20:1282248..1284954-chr20:1288783..1291101,2	MCF-7	breast:
4	chr20:1280644..1283563-chr20:1283914..1285559,2	MCF-7	breast:
5	chr20:1283698..1286846-chr20:1286878..1289632,3	K562	blood:
6	chr20:1296232..1299079-chr20:1367748..1370124,3	K562	blood:
7	chr20:1285641..1287786-chr20:1289716..1291902,2	K562	blood:
8	chr20:1283698..1286846-chr20:1286878..1289632,3	K562	blood:
9	chr20:1280644..1283563-chr20:1283914..1285559,2	MCF-7	breast:
10	chr20:1281423..1283535-chr20:1306063..1308157,2	K562	blood:
11	chr20:1286013..1291003-chr20:1304965..1309000,4	K562	blood:
12	chr20:1282248..1284954-chr20:1288783..1291101,2	MCF-7	breast:
13	chr20:1205295..1208138-chr20:1282456..1285112,2	K562	blood:
14	chr20:1279418..1283217-chr20:1283449..1287758,5	K562	blood:
15	chr20:1293745..1297831-chr20:1304825..1308186,3	MCF-7	breast:
16	chr20:1205252..1207423-chr20:1288622..1291157,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SNPH-3	chr20:1291041-1291229	NONHSAT078097
2	lnc-SNPH-3	chr20:1290266-1290556	NONHSAT078097

Variant related genes	Relation type
SDCBP2	TF binding region
SDCBP2	CpG island
ENSG00000234684	chromatin interactions
ENSG00000125775	chromatin interactions
ENSG00000244588	chromatin interactions
ENSG00000088832	chromatin interactions

Extended variants
information (count: 684 )
Associated
traits (count: 62 )

Variant overlapped rSNPs/rCNVs (count:684 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7354385	chr20:1283523-1283524	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs570464307	chr20:1283549-1283550	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs565976147	chr20:1283560-1283561	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs78239680	chr20:1283611-1283612	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs557958941	chr20:1283657-1283658	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs12624336	chr20:1283682-1283683	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs543607395	chr20:1283755-1283756	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs542719811	chr20:1283768-1283769	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs184697981	chr20:1283785-1283786	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs542615359	chr20:1283788-1283789	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs559074754	chr20:1283816-1283817	Weak transcription Genic enhancers Strong transcription ZNF genes & repeats Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs528033659	chr20:1283937-1283938	Weak transcription Genic enhancers Strong transcription ZNF genes & repeats Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs140474998	chr20:1283940-1283941	Weak transcription Genic enhancers Strong transcription ZNF genes & repeats Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs8125418	chr20:1283985-1283986	Weak transcription Genic enhancers Strong transcription ZNF genes & repeats Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs79723411	chr20:1284062-1284063	Weak transcription Genic enhancers Strong transcription ZNF genes & repeats Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs545271097	chr20:1284092-1284093	Weak transcription Genic enhancers Strong transcription ZNF genes & repeats Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs549937520	chr20:1284118-1284119	Weak transcription Genic enhancers Strong transcription ZNF genes & repeats Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs563444973	chr20:1284140-1284141	Weak transcription Genic enhancers Strong transcription ZNF genes & repeats Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs565268123	chr20:1284141-1284142	Weak transcription Genic enhancers Strong transcription ZNF genes & repeats Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs144917220	chr20:1284236-1284237	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs549399253	chr20:1284246-1284247	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs528119793	chr20:1284252-1284253	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs144865645	chr20:1284253-1284254	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs565938138	chr20:1284266-1284267	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs11906749	chr20:1284273-1284274	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs551714457	chr20:1284275-1284276	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs571538496	chr20:1284328-1284329	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs78602328	chr20:1284345-1284346	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs138746370	chr20:1284409-1284410	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs371250381	chr20:1284410-1284411	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs75971998	chr20:1284455-1284456	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs76077319	chr20:1284461-1284462	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs188676544	chr20:1284462-1284463	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs552963221	chr20:1284486-1284487	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs572736910	chr20:1284502-1284503	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs181295464	chr20:1284528-1284529	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs4814089	chr20:1284579-1284580	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs577869085	chr20:1284603-1284604	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs543617819	chr20:1284638-1284639	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs568450062	chr20:1284645-1284646	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs529436923	chr20:1284649-1284650	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs376801076	chr20:1284687-1284688	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs143556506	chr20:1284694-1284695	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs559763111	chr20:1284698-1284699	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs189507372	chr20:1284699-1284700	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs551753191	chr20:1284741-1284742	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs571572684	chr20:1284746-1284747	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs537330464	chr20:1284768-1284769	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs148022091	chr20:1284771-1284772	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs567325458	chr20:1284773-1284774	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:62)

Disease	PMID	Source
Hodgkin''s lymphoma	18641027	CNVD
Myelofibrosis	22110671	CNVD
Intellectual disability	22045946	CNVD
Glioblastoma multiforme	22286061	CNVD
Hepatocellular carcinoma	22174799	CNVD
Colorectal cancer	19455253	CNVD
Ovarian cancer	20844748	CNVD
Breast cancer	17603634	CNVD
Colorectal cancer	19359472	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Intracranial aneurysm	16715129	CNVD
Colorectal cancer	16774939	CNVD
Autism	18414403	CNVD
Neurocytoma	17123091	CNVD
Medulloblastoma	21979893	CNVD
Breast cancer	16397240	CNVD
abortions and stillbirths	19751515	CNVD
Wilms tumour	21544195	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	16272173	CNVD
Melanoma	18172304	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Oral cancer	19627613	CNVD
colon cancer	17210682	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	21080181	CNVD
Thyroid cancer	19087340	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	16751803	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Human rectal carcinomas	16397240	CNVD
Olfactory neuroblastoma	18408657	CNVD
Central neurocytomas	17123091	CNVD
Colorectal cancer	16272173	CNVD
Gastric cancer	17908304	CNVD
Urothelial carcinoma	21177765	CNVD
lymphocytic leukemia	21291569	CNVD
Acute myeloid leukemia	20729466	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Ewing''s sarcoma	17952124	CNVD
Oral cancer	21386901	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Lung cancer	18438408	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Colorectal cancer	21645411	CNVD
small cell lung cancer	20016488	CNVD
Melanoma	17363583	CNVD

Chromatin state (count:522 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr20:1253800-1285400	Weak transcription	Aorta	Aorta
2	chr20:1266400-1284800	Weak transcription	Brain Germinal Matrix	brain
3	chr20:1269200-1283600	Weak transcription	Right Ventricle	heart
4	chr20:1272200-1285400	Weak transcription	Adipose Nuclei	Adipose
5	chr20:1272200-1285400	Weak transcription	Left Ventricle	heart
6	chr20:1272200-1286000	Weak transcription	Sigmoid Colon	Sigmoid Colon
7	chr20:1272400-1285800	Weak transcription	Fetal Muscle Leg	muscle
8	chr20:1272600-1294000	Weak transcription	Rectal Smooth Muscle	rectum
9	chr20:1273000-1294000	Weak transcription	Skeletal Muscle Female	skeletal muscle
10	chr20:1274800-1288200	Weak transcription	Fetal Intestine Small	intestine
11	chr20:1275000-1289400	Weak transcription	Rectal Mucosa Donor 29	rectum
12	chr20:1275400-1284000	Weak transcription	Pancreas	Pancrea
13	chr20:1275800-1285400	Weak transcription	Duodenum Mucosa	Duodenum
14	chr20:1275800-1293800	Weak transcription	Brain Substantia Nigra	brain
15	chr20:1276600-1289800	Weak transcription	Pancreatic Islets	Pancreatic Islet
16	chr20:1278200-1294000	Weak transcription	Colon Smooth Muscle	Colon
17	chr20:1278800-1283600	Weak transcription	Fetal Brain Female	brain
18	chr20:1280600-1294000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
19	chr20:1281400-1289800	Weak transcription	Colonic Mucosa	Colon
20	chr20:1281600-1285600	Weak transcription	Brain Cingulate Gyrus	brain
21	chr20:1281600-1285600	Weak transcription	Brain Inferior Temporal Lobe	brain
22	chr20:1281600-1285800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
23	chr20:1281600-1290000	Weak transcription	Brain Hippocampus Middle	brain
24	chr20:1281800-1283600	Weak transcription	Cortex derived primary cultured neurospheres	brain
25	chr20:1281800-1283600	Weak transcription	Gastric	stomach
26	chr20:1281800-1285200	Weak transcription	Lung	lung
27	chr20:1281800-1294000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
28	chr20:1282000-1283600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
29	chr20:1282000-1283600	Weak transcription	HSMM	muscle
30	chr20:1282000-1283800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
31	chr20:1282000-1284000	Weak transcription	Brain Anterior Caudate	brain
32	chr20:1282000-1284600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
33	chr20:1282000-1284600	Weak transcription	Fetal Stomach	stomach
34	chr20:1282000-1285800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
35	chr20:1282000-1285800	Weak transcription	Muscle Satellite Cultured Cells	--
36	chr20:1282000-1289000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
37	chr20:1282000-1293800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
38	chr20:1282000-1293800	Weak transcription	H9 Cell Line	embryonic stem cell
39	chr20:1282000-1294000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
40	chr20:1282000-1294400	Weak transcription	Stomach Mucosa	stomach
41	chr20:1282000-1298200	Weak transcription	A549	lung
42	chr20:1282200-1283600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
43	chr20:1282200-1283600	Weak transcription	Stomach Smooth Muscle	stomach
44	chr20:1282200-1284200	Weak transcription	Skeletal Muscle Male	skeletal muscle
45	chr20:1282200-1284400	Weak transcription	K562	blood
46	chr20:1282200-1285000	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
47	chr20:1282200-1285000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
48	chr20:1282200-1285400	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
49	chr20:1282200-1285400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
50	chr20:1282200-1285400	Weak transcription	Duodenum Smooth Muscle	Duodenum

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