Variant report

Variant	nsv833615
Chromosome Location	chr18:29008396-29192976
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2778)
CpG islands
(count:1405)
Chromatin interactive
region (count:88)
LncRNA
region (count:10)
Mature miRNA
region (count: 0)
miRNA target
sites (count:7)

(count:2778 , 50 per page) page: 1 2 3 4 5 6 7 ... 56

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr18:29077614-29077727	K562	blood:	n/a	n/a
2	ARID3A	chr18:29176005-29176447	HepG2	liver:	n/a	n/a
3	ARID3A	chr18:29079137-29079444	HepG2	liver:	n/a	chr18:29079218-29079234
4	ARID3A	chr18:29089591-29090755	HepG2	liver:	n/a	n/a
5	ARID3A	chr18:29171157-29172132	HepG2	liver:	n/a	n/a
6	ARID3A	chr18:29147012-29147181	HepG2	liver:	n/a	n/a
7	ARID3A	chr18:29166577-29167110	HepG2	liver:	n/a	chr18:29166636-29166652
8	ARID3A	chr18:29135862-29136374	HepG2	liver:	n/a	n/a
9	ARID3A	chr18:29016896-29016955	HepG2	liver:	n/a	n/a
10	ARID3A	chr18:29113255-29113630	HepG2	liver:	n/a	n/a
11	ARID3A	chr18:29187408-29187649	HepG2	liver:	n/a	n/a
12	ARID3A	chr18:29167488-29167920	HepG2	liver:	n/a	n/a
13	ARID3A	chr18:29077601-29077799	HepG2	liver:	n/a	n/a
14	ARID3A	chr18:29186073-29186697	HepG2	liver:	n/a	n/a
15	ARID3A	chr18:29092091-29092828	HepG2	liver:	n/a	n/a
16	ARID3A	chr18:29080008-29080113	K562	blood:	n/a	n/a
17	ARID3A	chr18:29175473-29175517	HepG2	liver:	n/a	n/a
18	ARID3A	chr18:29135876-29136268	K562	blood:	n/a	n/a
19	ATF1	chr18:29043383-29043412	K562	blood:	n/a	n/a
20	ATF1	chr18:29092424-29092788	K562	blood:	n/a	n/a
21	ATF2	chr18:29073140-29073511	GM12878	blood:	n/a	n/a
22	ATF2	chr18:29070287-29070762	GM12878	blood:	n/a	n/a
23	ATF2	chr18:29018291-29018807	GM12878	blood:	n/a	n/a
24	ATF2	chr18:29073036-29073485	GM12878	blood:	n/a	n/a
25	ATF2	chr18:29080076-29080707	GM12878	blood:	n/a	n/a
26	ATF2	chr18:29018383-29018706	GM12878	blood:	n/a	n/a
27	ATF2	chr18:29079992-29080785	GM12878	blood:	n/a	n/a
28	ATF2	chr18:29070180-29070762	GM12878	blood:	n/a	n/a
29	ATF3	chr18:29092268-29092710	K562	blood:	n/a	chr18:29092605-29092620
30	BACH1	chr18:29134021-29134028	H1-hESC	embryonic stem cell:	n/a	n/a
31	BACH1	chr18:29077568-29078114	H1-hESC	embryonic stem cell:	n/a	n/a
32	BATF	chr18:29073201-29073632	GM12878	blood:	n/a	n/a
33	BATF	chr18:29080141-29080742	GM12878	blood:	n/a	n/a
34	BATF	chr18:29018420-29018737	GM12878	blood:	n/a	n/a
35	BATF	chr18:29018346-29018766	GM12878	blood:	n/a	n/a
36	BATF	chr18:29070334-29070694	GM12878	blood:	n/a	chr18:29070370-29070379
37	BATF	chr18:29070300-29070704	GM12878	blood:	n/a	chr18:29070370-29070379
38	BCL11A	chr18:29080431-29080697	GM12878	blood:	n/a	n/a
39	BCL11A	chr18:29018405-29018782	GM12878	blood:	n/a	n/a
40	BCL11A	chr18:29073158-29073654	GM12878	blood:	n/a	n/a
41	BCL11A	chr18:29073153-29073684	GM12878	blood:	n/a	n/a
42	BCL3	chr18:29018340-29018768	GM12878	blood:	n/a	n/a
43	BCL3	chr18:29073162-29073518	GM12878	blood:	n/a	n/a
44	BCLAF1	chr18:29079961-29080791	GM12878	blood:	n/a	n/a
45	BCLAF1	chr18:29073175-29073475	GM12878	blood:	n/a	n/a
46	BHLHE40	chr18:29092249-29092709	K562	blood:	n/a	n/a
47	BHLHE40	chr18:29077653-29078647	K562	blood:	n/a	n/a
48	BHLHE40	chr18:29092079-29092767	HepG2	liver:	n/a	n/a
49	BHLHE40	chr18:29063800-29063895	GM12878	blood:	n/a	n/a
50	BHLHE40	chr18:29092114-29092564	HepG2	liver:	n/a	n/a

(count:1405 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr18:29077698-29077748	HUVEC	blood vessel:	n/a
2	chr18:29178942-29178992	BE2_C	brain:	n/a
3	chr18:29077698-29077748	HUVEC	blood vessel:	n/a
4	chr18:29178942-29178992	BE2_C	brain:	n/a
5	chr18:29027701-29027751	AoSMC	blood vessel:	n/a
6	chr18:29026301-29026351	SK-N-SH_RA	brain:	n/a
7	chr18:29076604-29076654	ovcar-3	ovarian:	n/a
8	chr18:29171878-29171928	GM06990	blood:	n/a
9	chr18:29027885-29027935	AG04450	lung:	fetal
10	chr18:29077863-29077913	LNCaP	prostate:	n/a
11	chr18:29027658-29027708	HMEC	breast:	n/a
12	chr18:29078241-29078291	HEK293	kidney:	embryo
13	chr18:29078565-29078615	Hepatocyte	liver:	n/a
14	chr18:29027658-29027708	AoSMC	blood vessel:	n/a
15	chr18:29027885-29027935	BJ	skin:	n/a
16	chr18:29077698-29077748	SK-N-SH	brain:	n/a
17	chr18:29170928-29170978	SK-N-SH_RA	brain:	n/a
18	chr18:29027885-29027935	HRPEpiC	eye:	n/a
19	chr18:29026303-29026353	Caco-2	colon:	n/a
20	chr18:29170928-29170978	LNCaP	prostate:	n/a
21	chr18:29171977-29172027	HepG2	liver:	n/a
22	chr18:29026303-29026353	SKMC	muscle:	n/a
23	chr18:29171545-29171595	HEK293	kidney:	embryo
24	chr18:29078241-29078291	RPTEC	kidney:	n/a
25	chr18:29080595-29080645	GM12891	blood:	n/a
26	chr18:29170604-29170654	NH-A	brain:	n/a
27	chr18:29171878-29171928	SK-N-MC	brain:	n/a
28	chr18:29080265-29080315	HUVEC	blood vessel:	n/a
29	chr18:29027885-29027935	HPAEpiC	pulmonary alveolar:	n/a
30	chr18:29078565-29078615	Caco-2	colon:	n/a
31	chr18:29026301-29026351	T-47D	breast:	n/a
32	chr18:29170928-29170978	GM06990	blood:	n/a
33	chr18:29178454-29178504	HRE	kidney:	n/a
34	chr18:29027658-29027708	HRCEpiC	kidney:	n/a
35	chr18:29027701-29027751	NH-A	brain:	n/a
36	chr18:29078241-29078291	PFSK-1	brain:	n/a
37	chr18:29026303-29026353	CMK	blood:	n/a
38	chr18:29026301-29026351	PrEC	prostate:	n/a
39	chr18:29170928-29170978	PANC-1	pancreas:	n/a
40	chr18:29077863-29077913	HAEpiC	amniotic membrane:	n/a
41	chr18:29178942-29178992	H1-hESC	embryonic stem cell:	embryo
42	chr18:29171545-29171595	HRCEpiC	kidney:	n/a
43	chr18:29171545-29171595	BE2_C	brain:	n/a
44	chr18:29026303-29026353	AG04450	lung:	fetal
45	chr18:29178454-29178504	SK-N-SH_RA	brain:	n/a
46	chr18:29078565-29078615	HepG2	liver:	n/a
47	chr18:29077698-29077748	Hela-S3	cervix:	n/a
48	chr18:29127091-29127141	HRCEpiC	kidney:	n/a
49	chr18:29076604-29076654	HRCEpiC	kidney:	n/a
50	chr18:29171977-29172027	SKMC	muscle:	n/a

(count:88 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr18:29070302..29073813-chr18:29076378..29079026,4	MCF-7	breast:
2	chr18:29062010..29063666-chr18:29066941..29068808,2	K562	blood:
3	chr18:29070292..29073847-chr18:29075738..29079463,4	K562	blood:
4	chr18:29062010..29063666-chr18:29066941..29068808,2	K562	blood:
5	chr18:29003994..29005325-chr18:29086073..29087125,6	MCF-7	breast:
6	chr18:29098189..29101114-chr18:29103613..29106437,2	MCF-7	breast:
7	chr18:29065171..29067797-chr18:29078950..29080712,2	K562	blood:
8	chr18:29078512..29082072-chr18:29089360..29094851,6	K562	blood:
9	chr18:29068168..29070784-chr18:29076048..29078147,2	K562	blood:
10	chr18:29082210..29085319-chr18:29089707..29093199,4	K562	blood:
11	chr18:29004154..29005000-chr18:29143490..29144004,2	K562	blood:
12	chr18:28846335..28847118-chr18:29086087..29086880,3	MCF-7	breast:
13	chr18:29003997..29005002-chr18:29143774..29144455,3	MCF-7	breast:
14	chr18:29079215..29080950-chr18:29081744..29084257,2	MCF-7	breast:
15	chr18:29058662..29063697-chr18:29063884..29065891,5	K562	blood:
16	chr18:29077257..29078903-chr18:29144506..29147477,2	MCF-7	breast:
17	chr18:29056016..29057570-chr18:29059465..29061281,2	K562	blood:
18	chr18:29033071..29035215-chr18:29036604..29039421,3	K562	blood:
19	chr18:29080297..29083464-chr18:29083547..29086345,4	K562	blood:
20	chr18:29112621..29114426-chr18:29114667..29118167,3	K562	blood:
21	chr18:29135862..29136519-chr5:43095462..43095982,3	MCF-7	breast:
22	chr18:29135071..29136376-chr18:29302039..29303290,3	MCF-7	breast:
23	chr18:29076737..29079716-chr18:29083540..29087403,5	K562	blood:
24	chr18:29077877..29084482-chr18:29088955..29095937,13	K562	blood:
25	chr18:29056016..29057570-chr18:29059465..29061281,2	K562	blood:
26	chr18:29062053..29064443-chr18:29081495..29083582,3	K562	blood:
27	chr18:29068752..29071565-chr18:29076556..29079913,5	MCF-7	breast:
28	chr11:71823410..71824011-chr18:29077781..29078468,2	Hela-S3	cervix:
29	chr18:29066393..29069517-chr18:29071339..29073369,4	K562	blood:
30	chr18:29089902..29091907-chr18:29103774..29106283,2	MCF-7	breast:
31	chr18:29038496..29040369-chr18:29042094..29044336,2	K562	blood:
32	chr18:28932546..28935472-chr18:29078101..29080400,2	K562	blood:
33	chr18:28820916..28822485-chr18:29145187..29146692,2	K562	blood:
34	chr18:29058662..29063697-chr18:29063884..29065891,5	K562	blood:
35	chr18:29079737..29082965-chr18:29084557..29087491,4	K562	blood:
36	chr18:29114657..29116282-chr18:29138733..29141609,2	K562	blood:
37	chr18:29042545..29045965-chr18:29077171..29079744,3	K562	blood:
38	chr18:29065343..29067294-chr18:29076148..29078028,2	MCF-7	breast:
39	chr18:28680816..28682711-chr18:29076315..29078384,2	K562	blood:
40	chr18:29033071..29035215-chr18:29036604..29039421,3	K562	blood:
41	chr18:29003931..29004668-chr18:29134416..29135171,2	MCF-7	breast:
42	chr18:29089738..29092422-chr18:29128090..29130094,2	MCF-7	breast:
43	chr18:29065798..29067835-chr18:29072600..29075052,2	K562	blood:
44	chr18:29145542..29146264-chr18:29205706..29207014,3	MCF-7	breast:
45	chr18:29077683..29079249-chr18:29092433..29094661,2	MCF-7	breast:
46	chr18:28786778..28788708-chr18:29017378..29018896,2	MCF-7	breast:
47	chr18:29007636..29009624-chr18:29016577..29018951,2	MCF-7	breast:
48	chr18:29038234..29040822-chr18:29041279..29043976,2	MCF-7	breast:
49	chr18:29076759..29079471-chr18:29120956..29123046,2	K562	blood:
50	chr18:29080297..29083464-chr18:29083547..29086345,4	K562	blood:

(count:10 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-B4GALT6-2	chr18:29065357-29065747	XLOC_012803
2	lnc-B4GALT6-1	chr18:29130095-29130322	ENSG00000264859.1
3	lnc-B4GALT6-1	chr18:29122222-29122284	NONHSAT058824
4	lnc-B4GALT6-1	chr18:29123065-29123360	NONHSAT058824
5	lnc-B4GALT6-2	chr18:29076934-29076959	XLOC_012803
6	lnc-B4GALT6-2	chr18:29076608-29076815	ENSG00000266521.1
7	lnc-B4GALT6-1	chr18:29135926-29136084	ENSG00000264859.1
8	lnc-B4GALT6-1	chr18:29134605-29134678	ENSG00000264859.1
9	lnc-B4GALT6-1	chr18:29136520-29136868	ENSG00000264859.1
10	lnc-B4GALT6-2	chr18:29076934-29077158	ENSG00000266521.1

No data

(count:7 , 50 per page) page: 1

No.	miRNA target gene	miRNA name	Chromosome Location
1	DSG2	hsa-miR-30a-5p	chr18:29128479-29128503
2	DSG2	hsa-miR-30a-5p	chr18:29127961-29127982
3	DSG2	hsa-miR-155-5p	chr18:29127332-29127354
4	DSG2	hsa-miR-15b-5p	chr18:29126914-29126935
5	DSG2	hsa-miR-124-3p	chr18:29126938-29126944
6	DSG2	hsa-miR-155-5p	chr18:29127653-29127675
7	DSG2	hsa-miR-124-3p	chr18:29126926-29126945

Variant related genes	Relation type
DSG2	TF binding region
TTR	TF binding region
ENSG00000264859	TF binding region
DSG3	TF binding region
ENSG00000266521	TF binding region
ENSG00000266729	TF binding region
DSG2	CpG island
TTR	CpG island
ENSG00000264859	CpG island
DSG3	CpG island
ENSG00000266521	CpG island
ENSG00000266729	CpG island
ENSG00000264859	chromatin interactions
ENSG00000110200	chromatin interactions
ENSG00000265888	chromatin interactions
ENSG00000046604	chromatin interactions
ENSG00000266521	chromatin interactions
ENSG00000134755	chromatin interactions
ENSG00000266729	chromatin interactions
FPGS	miRNA target sites
FRAS1	miRNA target sites

Extended variants
information (count: 7349 )
Associated
traits (count: 73 )

Variant overlapped rSNPs/rCNVs (count:7349 , 50 per page) page: 1 2 3 4 5 6 7 ... 147

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs532806183	chr18:29008400-29008401	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs557344920	chr18:29008411-29008412	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs117282627	chr18:29008485-29008486	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs543308440	chr18:29008487-29008488	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs371213077	chr18:29008589-29008590	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs117618570	chr18:29008594-29008595	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs539986000	chr18:29008595-29008596	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs2613140	chr18:29008626-29008627	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs564981542	chr18:29008669-29008670	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs116882228	chr18:29008674-29008675	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs2613139	chr18:29008684-29008685	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs375152885	chr18:29008746-29008747	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs180923157	chr18:29008762-29008763	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs78446343	chr18:29008835-29008836	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs116157932	chr18:29008840-29008841	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs560962634	chr18:29008911-29008912	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs185977288	chr18:29008941-29008942	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs566584180	chr18:29008963-29008964	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs141895152	chr18:29008984-29008985	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs146080266	chr18:29008997-29008998	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs540216725	chr18:29008999-29009000	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs140074496	chr18:29009001-29009002	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs539093312	chr18:29009018-29009019	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs557407780	chr18:29009023-29009024	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs190261800	chr18:29009061-29009062	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs4485444	chr18:29009076-29009077	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs57165896	chr18:29009129-29009130	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs368652401	chr18:29009145-29009146	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs372712356	chr18:29009163-29009164	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs540826939	chr18:29009175-29009176	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs114271811	chr18:29009239-29009240	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs532096378	chr18:29009278-29009279	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs112998509	chr18:29009286-29009287	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs77249630	chr18:29009317-29009318	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs111677540	chr18:29009341-29009342	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs369423376	chr18:29009354-29009355	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs143823386	chr18:29009389-29009390	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs112941140	chr18:29009396-29009397	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs12961029	chr18:29009409-29009410	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs146359281	chr18:29009459-29009460	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs557827981	chr18:29009497-29009498	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs570519735	chr18:29009517-29009518	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs539156266	chr18:29009563-29009564	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs531279149	chr18:29009608-29009609	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs570150471	chr18:29009628-29009629	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs182537022	chr18:29009652-29009653	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs72929966	chr18:29009675-29009676	Enhancers Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs186259788	chr18:29009694-29009695	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs139417809	chr18:29009705-29009706	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs555808715	chr18:29009719-29009720	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:73)

Disease	PMID	Source
Esophageal squamous carcinoma	18350619	CNVD
Follicular lymphoma	20505157	CNVD
Chordoma	21602918	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	18923191	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Cancer	21637783	CNVD
Medulloblastoma	21979893	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Trisomy 18 syndrome	17576883	CNVD
lymphocytic leukemia	21291569	CNVD
Barrett''s syndrome	19417022	CNVD
Ewing''s sarcoma	17952124	CNVD
Multiple myeloma	17550852	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Glioblastoma multiforme	21922591	CNVD
Melanoma	18172304	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Lung cancer	18438408	CNVD
18q deletion syndrome	19533772	CNVD
Acute myeloid leukemia	16864856	CNVD
Colorectal cancer	21102417	CNVD
Colorectal cancer	20709793	CNVD
Pancreatic cancer	21811562	CNVD
Basal cell lymphoma	21115979	CNVD
Mucosa-associated lymphoid tissue lymphomas	21459788	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Oligodendroglial tumors	17285580	CNVD
colon cancer	17210682	CNVD
Breast cancer	21785460	CNVD
Hepatocellular carcinoma	16750200	CNVD
Prostate cancer	16573809	CNVD
Autism	16446308	CNVD
Colorectal cancer	19359472	CNVD
Colorectal cancer	16272173	CNVD
Human rectal carcinomas	16397240	CNVD
Medulloblastoma	18056178	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Cancer	16751803	CNVD
Metanephric adenoma	20802469	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	17133270	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Colorectal cancer	16774939	CNVD
Colorectal cancer	21297112	CNVD
Myelofibrosis	22110671	CNVD
Colorectal cancer	21645411	CNVD
Glioblastoma multiforme	17002787	CNVD
Cancer	21183584	CNVD
Breast cancer	17603634	CNVD
Thyroid cancer	19087340	CNVD
Urothelial carcinoma	21177765	CNVD
Oral cancer	21386901	CNVD
Colorectal cancer	16912164	CNVD
Renal cell carcinoma	19150565	CNVD
Multiple myeloma	16616336	CNVD
Colorectal cancer	19150955	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	21364760	CNVD
Pancreatic cancer	21811587	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Prostate cancer	22341455	CNVD
early-passage human iPS cells	21368824	CNVD

Chromatin state (count:1984 , 50 per page) page: 1 2 3 4 5 6 7 ... 40

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr18:29004400-29009200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
2	chr18:29006600-29010600	Enhancers	Placenta Amnion	Placenta Amnion
3	chr18:29007200-29008800	Weak transcription	HMEC	breast
4	chr18:29007200-29010800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
5	chr18:29007400-29008400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
6	chr18:29007400-29010800	Enhancers	NHEK	skin
7	chr18:29008200-29010600	Enhancers	Stomach Mucosa	stomach
8	chr18:29008200-29010800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
9	chr18:29008400-29009800	Enhancers	Breast Myoepithelial Primary Cells	Breast
10	chr18:29008400-29010600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
11	chr18:29008800-29009600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
12	chr18:29008800-29010600	Enhancers	HMEC	breast
13	chr18:29009000-29009400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
14	chr18:29009000-29010400	Enhancers	Rectal Mucosa Donor 31	rectum
15	chr18:29009200-29009400	Enhancers	Small Intestine	intestine
16	chr18:29009200-29010200	Enhancers	iPS-15b Cell Line	embryonic stem cell
17	chr18:29009200-29010200	Enhancers	Fetal Intestine Large	intestine
18	chr18:29009200-29010400	Enhancers	ES-I3 Cell Line	embryonic stem cell
19	chr18:29009200-29010600	Enhancers	Hela-S3	cervix
20	chr18:29009400-29009800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
21	chr18:29009400-29010400	Enhancers	HUES6 Cell Line	embryonic stem cell
22	chr18:29009600-29010200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
23	chr18:29009800-29010200	Enhancers	ES-WA7 Cell Line	embryonic stem cell
24	chr18:29009800-29010400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
25	chr18:29010000-29010200	Enhancers	Small Intestine	intestine
26	chr18:29010200-29010400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
27	chr18:29010600-29012200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
28	chr18:29010800-29019800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
29	chr18:29012200-29012600	ZNF genes & repeats	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
30	chr18:29012600-29016800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
31	chr18:29016800-29017400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
32	chr18:29017200-29017400	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
33	chr18:29019600-29020400	Enhancers	Primary monocytes fromperipheralblood	blood
34	chr18:29019800-29020200	Enhancers	Monocytes-CD14+_RO01746	blood
35	chr18:29019800-29020600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
36	chr18:29019800-29020800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
37	chr18:29019800-29020800	Enhancers	NHEK	skin
38	chr18:29020400-29022400	Weak transcription	Primary monocytes fromperipheralblood	blood
39	chr18:29020600-29021000	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
40	chr18:29020800-29021800	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
41	chr18:29020800-29021800	Flanking Active TSS	NHEK	skin
42	chr18:29021000-29021400	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
43	chr18:29021400-29021800	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
44	chr18:29021800-29022200	Enhancers	NHEK	skin
45	chr18:29021800-29026800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
46	chr18:29022200-29022600	Weak transcription	NHEK	skin
47	chr18:29022400-29023000	Enhancers	Primary monocytes fromperipheralblood	blood
48	chr18:29022600-29022800	Enhancers	NHEK	skin
49	chr18:29022800-29026600	Weak transcription	NHEK	skin
50	chr18:29024400-29024800	Enhancers	Esophagus	oesophagus

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