Variant report

Variant	esv3338881
Chromosome Location	chr1:228674354-228676902
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:675)
CpG islands
(count:672)
Chromatin interactive
region (count:20)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:675 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:228674601-228675035	K562	blood:	n/a	n/a
2	ARID3A	chr1:228674400-228674494	HepG2	liver:	n/a	n/a
3	ARID3A	chr1:228676599-228676669	K562	blood:	n/a	n/a
4	ATF1	chr1:228674430-228675080	K562	blood:	n/a	n/a
5	ATF2	chr1:228674483-228675022	H1-hESC	embryonic stem cell:	n/a	n/a
6	ATF2	chr1:228674256-228675042	GM12878	blood:	n/a	n/a
7	ATF2	chr1:228674527-228675088	H1-hESC	embryonic stem cell:	n/a	n/a
8	ATF2	chr1:228674284-228675029	GM12878	blood:	n/a	n/a
9	ATF3	chr1:228674224-228674960	A549	lung:	n/a	n/a
10	ATF3	chr1:228674546-228674994	K562	blood:	n/a	n/a
11	ATF3	chr1:228674496-228675012	A549	lung:	n/a	n/a
12	BACH1	chr1:228674278-228675008	K562	blood:	n/a	n/a
13	BACH1	chr1:228674184-228675065	H1-hESC	embryonic stem cell:	n/a	n/a
14	BCL3	chr1:228674197-228675191	A549	lung:	n/a	chr1:228675176-228675189 chr1:228674539-228674548 chr1:228675169-228675182
15	BCLAF1	chr1:228674201-228675044	GM12878	blood:	n/a	chr1:228674539-228674548
16	BHLHE40	chr1:228674301-228675258	HepG2	liver:	n/a	chr1:228675174-228675190 chr1:228675171-228675187
17	BHLHE40	chr1:228674214-228675144	K562	blood:	n/a	n/a
18	BHLHE40	chr1:228674301-228675052	GM12878	blood:	n/a	n/a
19	BHLHE40	chr1:228675520-228675720	K562	blood:	n/a	n/a
20	BHLHE40	chr1:228676504-228676617	K562	blood:	n/a	n/a
21	BHLHE40	chr1:228675520-228675780	GM12878	blood:	n/a	n/a
22	BHLHE40	chr1:228674596-228674998	A549	lung:	n/a	n/a
23	BRCA1	chr1:228674719-228675019	GM12878	blood:	n/a	n/a
24	BRCA1	chr1:228674287-228674462	GM12878	blood:	n/a	n/a
25	BRCA1	chr1:228674408-228675027	Hela-S3	cervix:	n/a	n/a
26	BRCA1	chr1:228674631-228674993	H1-hESC	embryonic stem cell:	n/a	n/a
27	CBX3	chr1:228674087-228675164	K562	blood:	n/a	n/a
28	CBX3	chr1:228674507-228675085	K562	blood:	n/a	n/a
29	CCNT2	chr1:228676216-228676468	K562	blood:	n/a	chr1:228676247-228676256
30	CCNT2	chr1:228674260-228675827	K562	blood:	n/a	n/a
31	CEBPB	chr1:228674416-228675259	Hela-S3	cervix:	n/a	n/a
32	CEBPB	chr1:228674634-228675016	H1-hESC	embryonic stem cell:	n/a	n/a
33	CEBPB	chr1:228674306-228674991	K562	blood:	n/a	n/a
34	CEBPB	chr1:228674196-228675004	GM12878	blood:	n/a	n/a
35	CEBPD	chr1:228674969-228675256	HepG2	liver:	n/a	n/a
36	CEBPD	chr1:228674364-228675205	K562	blood:	n/a	n/a
37	CHD1	chr1:228675177-228675371	GM12878	blood:	n/a	n/a
38	CHD1	chr1:228674573-228674885	H1-hESC	embryonic stem cell:	n/a	n/a
39	CHD1	chr1:228674193-228674928	GM12878	blood:	n/a	n/a
40	CHD2	chr1:228674363-228675032	H1-hESC	embryonic stem cell:	n/a	n/a
41	CHD2	chr1:228674325-228674359	HepG2	liver:	n/a	n/a
42	CHD2	chr1:228675826-228676011	GM12878	blood:	n/a	n/a
43	CHD2	chr1:228674216-228675146	GM12878	blood:	n/a	n/a
44	CHD2	chr1:228675713-228676039	Hela-S3	cervix:	n/a	n/a
45	CHD2	chr1:228674248-228675305	Hela-S3	cervix:	n/a	n/a
46	CHD2	chr1:228674233-228675027	K562	blood:	n/a	n/a
47	CHD2	chr1:228674595-228674960	HepG2	liver:	n/a	n/a
48	CREB1	chr1:228674189-228675344	A549	lung:	n/a	n/a
49	CREB1	chr1:228674101-228675188	HepG2	liver:	n/a	n/a
50	CREB1	chr1:228674393-228675159	ECC-1	luminal epithelium:	n/a	n/a

(count:672 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:228675139-228675189	HNPCEpiC	eye:	n/a
2	chr1:228675139-228675189	HNPCEpiC	eye:	n/a
3	chr1:228675901-228675951	HepG2	liver:	n/a
4	chr1:228676532-228676582	NB4	blood:	n/a
5	chr1:228675901-228675951	U87	brain:	n/a
6	chr1:228674907-228674957	GM12891	blood:	n/a
7	chr1:228675670-228675720	SK-N-MC	brain:	n/a
8	chr1:228675670-228675720	HAEpiC	amniotic membrane:	n/a
9	chr1:228674880-228674930	ECC-1	luminal epithelium:	n/a
10	chr1:228674907-228674957	ovcar-3	ovarian:	n/a
11	chr1:228675123-228675173	BJ	skin:	n/a
12	chr1:228674594-228674644	NB4	blood:	n/a
13	chr1:228675123-228675173	HNPCEpiC	eye:	n/a
14	chr1:228674880-228674930	Jurkat	blood:	n/a
15	chr1:228674909-228674959	GM06990	blood:	n/a
16	chr1:228674909-228674959	AG10803	skin:	n/a
17	chr1:228674966-228675016	BE2_C	brain:	n/a
18	chr1:228675901-228675951	NH-A	brain:	n/a
19	chr1:228674817-228674867	Jurkat	blood:	n/a
20	chr1:228674966-228675016	AoSMC	blood vessel:	n/a
21	chr1:228675901-228675951	NT2-D1	testis:	n/a
22	chr1:228675139-228675189	HCT-116	colon:	n/a
23	chr1:228674966-228675016	HCF	heart:	n/a
24	chr1:228675123-228675173	T-47D	breast:	n/a
25	chr1:228674909-228674959	Hela-S3	cervix:	n/a
26	chr1:228674966-228675016	SK-N-MC	brain:	n/a
27	chr1:228675670-228675720	SK-N-SH	brain:	n/a
28	chr1:228675123-228675173	CMK	blood:	n/a
29	chr1:228675670-228675720	NT2-D1	testis:	n/a
30	chr1:228674966-228675016	LNCaP	prostate:	n/a
31	chr1:228674909-228674959	ovcar-3	ovarian:	n/a
32	chr1:228674880-228674930	MCF10A-Er-Src	breast:	n/a
33	chr1:228674880-228674930	A549	lung:	n/a
34	chr1:228676532-228676582	HEEpiC	esophagus:	n/a
35	chr1:228674966-228675016	BJ	skin:	n/a
36	chr1:228674966-228675016	Jurkat	blood:	n/a
37	chr1:228676532-228676582	Jurkat	blood:	n/a
38	chr1:228675901-228675951	HEEpiC	esophagus:	n/a
39	chr1:228674907-228674957	SKMC	muscle:	n/a
40	chr1:228674880-228674930	HAEpiC	amniotic membrane:	n/a
41	chr1:228676532-228676582	GM06990	blood:	n/a
42	chr1:228674907-228674957	GM12878	blood:	n/a
43	chr1:228675901-228675951	GM12892	blood:	n/a
44	chr1:228674907-228674957	HIPEpiC	eye:	n/a
45	chr1:228674817-228674867	AG04449	skin:	fetal
46	chr1:228674594-228674644	H1-hESC	embryonic stem cell:	embryo
47	chr1:228675139-228675189	AoSMC	blood vessel:	n/a
48	chr1:228674594-228674644	MCF10A-Er-Src	breast:	n/a
49	chr1:228674817-228674867	AG10803	skin:	n/a
50	chr1:228675901-228675951	GM19239	blood:	n/a

(count:20 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:228642342..228647806-chr1:228672380..228678428,13	MCF-7	breast:
2	chr1:228675436..228678007-chr1:228697619..228700594,3	MCF-7	breast:
3	chr1:228672968..228678350-chr1:228679226..228685848,20	MCF-7	breast:
4	chr1:228645158..228646173-chr1:228673944..228674999,3	Hela-S3	cervix:
5	chr1:228673229..228674751-chr9:33024497..33026836,2	MCF-7	breast:
6	chr1:228487271..228488896-chr1:228674554..228676402,2	K562	blood:
7	chr1:228290240..228293064-chr1:228675062..228676582,2	K562	blood:
8	chr1:228673889..228674721-chr17:79935373..79935994,2	HCT-116	colon:
9	chr1:228671614..228676496-chr1:228676543..228681096,6	MCF-7	breast:
10	chr1:24285294..24286180-chr1:228675458..228676219,2	HCT-116	colon:
11	chr1:228671614..228676496-chr1:228676543..228681096,6	MCF-7	breast:
12	chr1:228674038..228674538-chr12:77157330..77158605,3	HCT-116	colon:
13	chr1:228592366..228594573-chr1:228675027..228676697,3	MCF-7	breast:
14	chr1:228643230..228649256-chr1:228671672..228678578,15	MCF-7	breast:
15	chr1:228321585..228323850-chr1:228673376..228675624,2	K562	blood:
16	chr1:228566145..228566967-chr1:228675038..228675653,2	MCF-7	breast:
17	chr1:228645191..228645823-chr1:228674602..228675559,2	K562	blood:
18	chr1:228400032..228401961-chr1:228675104..228677391,2	MCF-7	breast:
19	chr1:11967567..11969704-chr1:228673208..228675906,2	MCF-7	breast:
20	chr1:228674158..228676652-chr1:228698714..228701340,3	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RP5-915N17.9.1-2	chr1:228673895-228674821	NONHSAT010027

No data

Variant related genes	Relation type
RNF187	TF binding region
RNF187	CpG island
ENSG00000162913	chromatin interactions
ENSG00000154370	chromatin interactions
ENSG00000154358	chromatin interactions
ENSG00000196890	chromatin interactions
ENSG00000215811	chromatin interactions
ENSG00000086061	chromatin interactions
ENSG00000169696	chromatin interactions
ENSG00000143793	chromatin interactions
ENSG00000137074	chromatin interactions
ENSG00000189266	chromatin interactions
ENSG00000186908	chromatin interactions
ENSG00000188822	chromatin interactions
ENSG00000181218	chromatin interactions
ENSG00000199347	chromatin interactions
ENSG00000227625	chromatin interactions
ENSG00000168159	chromatin interactions

Extended variants
information (count: 101 )
Associated
traits (count: 91 )

Variant overlapped rSNPs/rCNVs (count:101 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs527785251	chr1:228674376-228674377	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region Chromatin interactive region lncRNA	11 gene(s)	Overlapped CNVs	n/a
2	rs113654288	chr1:228674384-228674385	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region Chromatin interactive region lncRNA	11 gene(s)	Overlapped CNVs	n/a
3	rs188183585	chr1:228674404-228674405	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region Chromatin interactive region lncRNA	11 gene(s)	Overlapped CNVs	n/a
4	rs567414907	chr1:228674429-228674430	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region Chromatin interactive region lncRNA	11 gene(s)	Overlapped CNVs	n/a
5	rs77508003	chr1:228674440-228674441	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region Chromatin interactive region lncRNA	11 gene(s)	Overlapped CNVs	n/a
6	rs192928462	chr1:228674443-228674444	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region Chromatin interactive region lncRNA	11 gene(s)	Overlapped CNVs	n/a
7	rs550327191	chr1:228674476-228674477	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region Chromatin interactive region lncRNA	11 gene(s)	Overlapped CNVs	n/a
8	rs4233233	chr1:228674518-228674519	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region Chromatin interactive region lncRNA	11 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs77493240	chr1:228674562-228674563	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region Chromatin interactive region lncRNA	11 gene(s)	Overlapped CNVs	n/a
10	rs527954265	chr1:228674572-228674573	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region Chromatin interactive region lncRNA	11 gene(s)	Overlapped CNVs	n/a
11	rs6684355	chr1:228674574-228674575	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region Chromatin interactive region lncRNA	11 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs144065794	chr1:228674588-228674589	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region Chromatin interactive region lncRNA	11 gene(s)	Overlapped CNVs	n/a
13	rs115141040	chr1:228674602-228674603	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	Overlapped CNVs	n/a
14	rs374257289	chr1:228674631-228674632	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	Overlapped CNVs	n/a
15	rs368970297	chr1:228674713-228674714	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region lncRNA	11 gene(s)	Overlapped CNVs	n/a
16	rs116220656	chr1:228674728-228674729	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region lncRNA	10 gene(s)	Overlapped CNVs	n/a
17	rs376622376	chr1:228674731-228674732	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region lncRNA	10 gene(s)	Overlapped CNVs	n/a
18	rs556294310	chr1:228674735-228674736	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region lncRNA	10 gene(s)	Overlapped CNVs	n/a
19	rs576271199	chr1:228674763-228674764	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region lncRNA	8 gene(s)	Overlapped CNVs	n/a
20	rs544858036	chr1:228674764-228674765	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region lncRNA	8 gene(s)	Overlapped CNVs	n/a
21	rs201367208	chr1:228674778-228674779	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region lncRNA	8 gene(s)	Overlapped CNVs	n/a
22	rs77412960	chr1:228674843-228674844	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
23	rs371700463	chr1:228674852-228674853	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
24	rs541014006	chr1:228674881-228674882	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
25	rs561253466	chr1:228674894-228674895	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
26	rs530181879	chr1:228674901-228674902	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
27	rs550124539	chr1:228674948-228674949	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
28	rs114220466	chr1:228674969-228674970	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
29	rs372162441	chr1:228674978-228674979	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
30	rs184610117	chr1:228674982-228674983	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
31	rs566366748	chr1:228674988-228674989	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
32	rs201911505	chr1:228675034-228675035	Active TSS Bivalent/Poised TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
33	rs188369530	chr1:228675065-228675066	Active TSS Bivalent/Poised TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
34	rs547392168	chr1:228675078-228675079	Active TSS Bivalent/Poised TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
35	rs567268935	chr1:228675130-228675131	Active TSS Bivalent/Poised TSS Flanking Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
36	rs536308340	chr1:228675246-228675247	Active TSS Bivalent/Poised TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
37	rs374893017	chr1:228675528-228675529	Active TSS Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
38	rs61827301	chr1:228675570-228675571	Active TSS Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	13 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs538439362	chr1:228675624-228675625	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
40	rs558459926	chr1:228675653-228675654	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
41	rs191528091	chr1:228675690-228675691	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region CpG island Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
42	rs571988188	chr1:228675718-228675719	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region CpG island Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
43	rs541048830	chr1:228675723-228675724	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
44	rs561302314	chr1:228675725-228675726	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
45	rs372128197	chr1:228675748-228675749	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
46	rs543850660	chr1:228675768-228675769	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
47	rs563626646	chr1:228675779-228675780	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
48	rs569004517	chr1:228675781-228675782	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
49	rs532794734	chr1:228675807-228675808	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
50	rs376912307	chr1:228675822-228675823	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:91)

Disease	PMID	Source
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Autism	22495311	CNVD
Melanoma	18172304	CNVD
Rett syndrome	21593744	CNVD
Medulloblastoma	21979893	CNVD
Cancer	20164919	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	CNVD
Non-small cell lung cancer	21044232	CNVD
Cervical cancer	21063398	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	20632083	CNVD
Endometrial cancer	22040021	CNVD
Ewing''s sarcoma	21437220	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	21080181	CNVD
Hepatocellular carcinoma	22174799	CNVD
Medulloblastoma	21292688	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	21264507	CNVD
Liposarcoma	21253554	CNVD
Multiple myeloma	21628407	CNVD
Cancer	16751803	CNVD
Prostate cancer	16705090	CNVD
Neuroblastoma	19435921	CNVD
Breast cancer	17850661	CNVD
Breast cancer	16461572	CNVD
Intracranial tumor	16823260	CNVD
Medulloblastoma	18056178	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Colorectal cancer	16272173	CNVD
Breast cancer	17603634	CNVD
Neuroblastoma	21899760	CNVD
Breast cancer	21858162	CNVD
Non-small cell lung cancer	21385341	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	16608533	CNVD
Ewing''s sarcoma	22429812	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17001317	CNVD
Acute myeloid leukemia	21251322	CNVD
Multiple myeloma	17550852	CNVD
Prostate cancer	18632612	CNVD
Acute myeloid leukemia	20729466	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Testicular germ cell tumor	18059402	CNVD
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
Neuroblastoma	18923191	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Breast cancer	21509527	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Urothelial carcinoma	21177765	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Chordoma	18071362	CNVD
T-cell lymphomas	19863542	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hepatocellular carcinoma	18803288	CNVD
Urothelial tumor	18831757	CNVD
Lung cancer	18438408	CNVD
Medulloblastoma	16783165	CNVD
Basal cell lymphoma	17170743	CNVD
Mental retardation	19951919	CNVD
Non-syndromic sensorineural hearing loss	17873649	CNVD
Basal cell lymphoma	17053054	CNVD
Autism	14699429	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Fumarase deficiency	21572526	CNVD
Autism	17483303	CNVD
Kartagener syndrome	16639409	CNVD
Congenital abnormalities	21549014	CNVD
Developmental delay	21549014	CNVD
Mental retardation	21549014	CNVD
small cell lung cancer	20016488	CNVD
Glioblastoma multiforme	21138945	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Cancer	20164920	CNVD
Cancer	17060936	CNVD
Myelofibrosis	22110671	CNVD
abnormal development	18461090	CNVD
Breast cancer	21364760	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Melanoma	17363583	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:460 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:228673600-228674600	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr1:228673600-228675800	Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
3	chr1:228673600-228675800	Active TSS	K562	blood
4	chr1:228673600-228676000	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
5	chr1:228673600-228676000	Active TSS	HUES6 Cell Line	embryonic stem cell
6	chr1:228673600-228676000	Active TSS	A549	lung
7	chr1:228673600-228676000	Active TSS	Hela-S3	cervix
8	chr1:228673600-228676200	Active TSS	H9 Cell Line	embryonic stem cell
9	chr1:228673800-228674400	Flanking Active TSS	Primary T cells fromperipheralblood	blood
10	chr1:228673800-228674400	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
11	chr1:228673800-228674400	Flanking Active TSS	Primary Natural Killer cells fromperipheralblood	blood
12	chr1:228673800-228674400	Active TSS	Brain Germinal Matrix	brain
13	chr1:228673800-228674400	Active TSS	Right Atrium	heart
14	chr1:228673800-228674400	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
15	chr1:228673800-228674400	Active TSS	NH-A	brain
16	chr1:228673800-228674600	Flanking Active TSS	Primary monocytes fromperipheralblood	blood
17	chr1:228673800-228674800	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
18	chr1:228673800-228675600	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
19	chr1:228673800-228675800	Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
20	chr1:228673800-228675800	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
21	chr1:228673800-228675800	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
22	chr1:228673800-228675800	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
23	chr1:228673800-228675800	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
24	chr1:228673800-228675800	Active TSS	Brain Hippocampus Middle	brain
25	chr1:228673800-228675800	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
26	chr1:228673800-228675800	Active TSS	Fetal Muscle Leg	muscle
27	chr1:228673800-228675800	Active TSS	GM12878-XiMat	blood
28	chr1:228673800-228676000	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
29	chr1:228673800-228676000	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
30	chr1:228673800-228676000	Active TSS	Breast Myoepithelial Primary Cells	Breast
31	chr1:228673800-228676000	Active TSS	Primary T cells from cord blood	blood
32	chr1:228673800-228676000	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
33	chr1:228673800-228676000	Active TSS	Muscle Satellite Cultured Cells	--
34	chr1:228673800-228676000	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
35	chr1:228673800-228676000	Active TSS	Aorta	Aorta
36	chr1:228673800-228676000	Active TSS	Brain Cingulate Gyrus	brain
37	chr1:228673800-228676000	Active TSS	Brain Inferior Temporal Lobe	brain
38	chr1:228673800-228676000	Active TSS	Colon Smooth Muscle	Colon
39	chr1:228673800-228676000	Active TSS	Duodenum Smooth Muscle	Duodenum
40	chr1:228673800-228676000	Active TSS	Fetal Intestine Large	intestine
41	chr1:228673800-228676000	Active TSS	Psoas Muscle	Psoas
42	chr1:228673800-228676000	Active TSS	Rectal Mucosa Donor 29	rectum
43	chr1:228673800-228676000	Active TSS	Rectal Smooth Muscle	rectum
44	chr1:228673800-228676000	Active TSS	NHEK	skin
45	chr1:228673800-228676200	Active TSS	Brain Angular Gyrus	brain
46	chr1:228673800-228676200	Active TSS	HSMM	muscle
47	chr1:228673800-228676200	Active TSS	NHLF	lung
48	chr1:228673800-228676600	Active TSS	HUES64 Cell Line	embryonic stem cell
49	chr1:228673800-228676600	Active TSS	iPS-18 Cell Line	embryonic stem cell
50	chr1:228673800-228676800	Active TSS	iPS-20b Cell Line	embryonic stem cell

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