Variant report

Variant	esv3375806
Chromosome Location	chr1:45189190-45191738
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:64)
CpG islands
(count:428)
Chromatin interactive
region (count:21)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:64 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr1:45189058-45189512	GM12878	blood:	n/a	n/a
2	ATF2	chr1:45188971-45189598	GM12878	blood:	n/a	n/a
3	BCLAF1	chr1:45188995-45189628	GM12878	blood:	n/a	chr1:45189390-45189399
4	EBF1	chr1:45189025-45189516	GM12878	blood:	n/a	n/a
5	EBF1	chr1:45189131-45189477	GM12878	blood:	n/a	n/a
6	EBF1	chr1:45189131-45189417	GM12878	blood:	n/a	n/a
7	EGR1	chr1:45190272-45190475	K562	blood:	n/a	chr1:45190394-45190404 chr1:45190395-45190404 chr1:45190356-45190369 chr1:45190394-45190407 chr1:45190394-45190407 chr1:45190394-45190407
8	EGR1	chr1:45190181-45190532	K562	blood:	n/a	chr1:45190394-45190404 chr1:45190395-45190404 chr1:45190356-45190369 chr1:45190394-45190407 chr1:45190394-45190407 chr1:45190394-45190407
9	EGR1	chr1:45189228-45189469	GM12878	blood:	n/a	n/a
10	ELF1	chr1:45189052-45189405	K562	blood:	n/a	n/a
11	ELF1	chr1:45188873-45189573	GM12878	blood:	n/a	n/a
12	ELK1	chr1:45189103-45189358	GM12878	blood:	n/a	n/a
13	EP300	chr1:45189253-45189345	GM12878	blood:	n/a	n/a
14	EP300	chr1:45188982-45189501	GM12878	blood:	n/a	n/a
15	ETS1	chr1:45189135-45189591	GM12878	blood:	n/a	chr1:45189390-45189403
16	FOXA1	chr1:45191093-45191432	HepG2	liver:	n/a	n/a
17	FOXM1	chr1:45189090-45189575	GM12878	blood:	n/a	n/a
18	HMGN3	chr1:45190306-45190323	K562	blood:	n/a	n/a
19	IKZF1	chr1:45188964-45189609	GM12878	blood:	n/a	n/a
20	IRF4	chr1:45188984-45189595	GM12878	blood:	n/a	n/a
21	IRF4	chr1:45189080-45189575	GM12878	blood:	n/a	n/a
22	MAX	chr1:45188846-45190776	NB4	blood:	n/a	n/a
23	MAX	chr1:45189012-45189460	GM12878	blood:	n/a	n/a
24	MEF2A	chr1:45189088-45189508	GM12878	blood:	n/a	chr1:45189392-45189400
25	MTA3	chr1:45188740-45189665	GM12878	blood:	n/a	n/a
26	MTA3	chr1:45188712-45189730	GM12878	blood:	n/a	n/a
27	MYC	chr1:45188879-45190790	NB4	blood:	n/a	n/a
28	NFIC	chr1:45188916-45189579	GM12878	blood:	n/a	n/a
29	NFIC	chr1:45189012-45189600	GM12878	blood:	n/a	n/a
30	NFYB	chr1:45189212-45189412	GM12878	blood:	n/a	n/a
31	PML	chr1:45189133-45189462	GM12878	blood:	n/a	n/a
32	PML	chr1:45188815-45189701	GM12878	blood:	n/a	n/a
33	POLR2A	chr1:45188941-45190728	NB4	blood:	n/a	n/a
34	POLR2A	chr1:45188746-45191415	HL-60	blood:	n/a	n/a
35	POLR2A	chr1:45188772-45191165	HL-60	blood:	n/a	n/a
36	POLR2A	chr1:45188846-45189598	GM12891	blood:	n/a	n/a
37	POLR2A	chr1:45189287-45189374	GM12878	blood:	n/a	n/a
38	POU2F2	chr1:45188864-45189506	GM12891	blood:	n/a	n/a
39	RCOR1	chr1:45188943-45189499	GM12878	blood:	n/a	n/a
40	RELA	chr1:45188946-45189552	GM19099	blood:	n/a	n/a
41	REST	chr1:45189056-45189387	Hela-S3	cervix:	n/a	n/a
42	RUNX3	chr1:45188731-45189576	GM12878	blood:	n/a	n/a
43	RUNX3	chr1:45188798-45189628	GM12878	blood:	n/a	n/a
44	SP1	chr1:45189107-45189528	GM12878	blood:	n/a	chr1:45189398-45189411
45	SP1	chr1:45189047-45189478	GM12878	blood:	n/a	chr1:45189398-45189411
46	SPI1	chr1:45188977-45189585	GM12891	blood:	n/a	chr1:45189379-45189392
47	SPI1	chr1:45188683-45189779	GM12878	blood:	n/a	chr1:45189379-45189392
48	SPI1	chr1:45188870-45189680	HL-60	blood:	n/a	chr1:45189379-45189392
49	SPI1	chr1:45188939-45189517	HL-60	blood:	n/a	chr1:45189379-45189392
50	SPI1	chr1:45188994-45189515	GM12878	blood:	n/a	chr1:45189379-45189392

(count:428 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:45189875-45189925	ProgFib	skin:	n/a
2	chr1:45189875-45189925	ProgFib	skin:	n/a
3	chr1:45191110-45191160	NT2-D1	testis:	n/a
4	chr1:45190912-45190962	MCF10A-Er-Src	breast:	n/a
5	chr1:45190297-45190347	SKMC	muscle:	n/a
6	chr1:45189743-45189793	IMR90	lung:	fetal
7	chr1:45190912-45190962	AG04450	lung:	fetal
8	chr1:45189743-45189793	MCF10A-Er-Src	breast:	n/a
9	chr1:45190519-45190569	MCF-7	breast:	n/a
10	chr1:45190297-45190347	IMR90	lung:	fetal
11	chr1:45190262-45190312	Caco-2	colon:	n/a
12	chr1:45189743-45189793	NHDF-neo	bronchial:	n/a
13	chr1:45190297-45190347	HIPEpiC	eye:	n/a
14	chr1:45190519-45190569	BE2_C	brain:	n/a
15	chr1:45191110-45191160	Jurkat	blood:	n/a
16	chr1:45191110-45191160	Caco-2	colon:	n/a
17	chr1:45190519-45190569	U87	brain:	n/a
18	chr1:45190519-45190569	PFSK-1	brain:	n/a
19	chr1:45189875-45189925	HEEpiC	esophagus:	n/a
20	chr1:45190297-45190347	AG09319	gingival:	n/a
21	chr1:45189875-45189925	AoSMC	blood vessel:	n/a
22	chr1:45189743-45189793	HCPEpiC	choroid plexus:	n/a
23	chr1:45190519-45190569	SAEC	small airway:	n/a
24	chr1:45190297-45190347	Hepatocyte	liver:	n/a
25	chr1:45189743-45189793	HCM	heart:	n/a
26	chr1:45189875-45189925	BJ	skin:	n/a
27	chr1:45189875-45189925	HRCEpiC	kidney:	n/a
28	chr1:45190912-45190962	HMEC	breast:	n/a
29	chr1:45190262-45190312	U87	brain:	n/a
30	chr1:45191110-45191160	NB4	blood:	n/a
31	chr1:45190912-45190962	HCF	heart:	n/a
32	chr1:45190519-45190569	GM12892	blood:	n/a
33	chr1:45190519-45190569	PANC-1	pancreas:	n/a
34	chr1:45190297-45190347	AoSMC	blood vessel:	n/a
35	chr1:45190519-45190569	AoSMC	blood vessel:	n/a
36	chr1:45190912-45190962	Caco-2	colon:	n/a
37	chr1:45190297-45190347	Jurkat	blood:	n/a
38	chr1:45190519-45190569	T-47D	breast:	n/a
39	chr1:45189875-45189925	NHBE	bronchial:	n/a
40	chr1:45189875-45189925	NH-A	brain:	n/a
41	chr1:45190262-45190312	Hela-S3	cervix:	n/a
42	chr1:45190912-45190962	HCM	heart:	n/a
43	chr1:45189743-45189793	GM19239	blood:	n/a
44	chr1:45191110-45191160	NHBE	bronchial:	n/a
45	chr1:45189875-45189925	HPAEpiC	pulmonary alveolar:	n/a
46	chr1:45191110-45191160	SK-N-SH	brain:	n/a
47	chr1:45190912-45190962	LNCaP	prostate:	n/a
48	chr1:45190912-45190962	Hela-S3	cervix:	n/a
49	chr1:45190262-45190312	Hepatocyte	liver:	n/a
50	chr1:45190912-45190962	CMK	blood:	n/a

(count:21 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:45190717..45192920-chr1:45241630..45243711,3	MCF-7	breast:
2	chr1:45184334..45189289-chr1:45475449..45480431,12	K562	blood:
3	chr1:45187273..45189411-chr14:24581564..24584245,2	MCF-7	breast:
4	chr1:45185676..45189343-chr1:46151396..46155571,4	K562	blood:
5	chr1:45184712..45189957-chr1:45986029..45989344,7	K562	blood:
6	chr1:45186940..45189725-chr3:64007164..64009117,2	MCF-7	breast:
7	chr1:45184399..45189674-chr1:45270870..45279135,15	MCF-7	breast:
8	chr1:45187439..45189397-chr1:145382385..145384052,2	K562	blood:
9	chr1:45187577..45189400-chr1:45255993..45258974,2	MCF-7	breast:
10	chr1:45178001..45208867-chr1:45262751..45305400,520	K562	blood:
11	chr1:45178748..45209946-chr1:45262890..45299284,515	K562	blood:
12	chr1:44494778..44496381-chr1:45187720..45189290,2	K562	blood:
13	chr1:45184864..45189212-chr1:45804136..45808316,8	K562	blood:
14	chr1:45179633..45191596-chr1:45283435..45288613,20	MCF-7	breast:
15	chr1:45184334..45189303-chr1:45475138..45480545,18	K562	blood:
16	chr1:45095364..45099259-chr1:45185766..45189852,13	K562	blood:
17	chr1:45190324..45200952-chr1:45272085..45288310,59	MCF-7	breast:
18	chr1:45187347..45189576-chr18:3253847..3255947,2	K562	blood:
19	chr1:45086647..45106769-chr1:45179099..45192041,56	K562	blood:
20	chr1:45186381..45189343-chr12:121198720..121200674,2	K562	blood:
21	chr1:45183794..45190315-chr1:45281186..45287888,32	MCF-7	breast:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-KIF2C-3	chr1:45189467-45189578	NONHSAT002888
2	lnc-KIF2C-3	chr1:45189503-45189578	NONHSAT002889
3	lnc-KIF2C-3	chr1:45189657-45190034	NONHSAT002889
4	lnc-KIF2C-3	chr1:45189794-45189976	NONHSAT002888

No data

Variant related genes	Relation type
C1orf228	TF binding region
RNU5F-1	TF binding region
C1orf228	CpG island
RNU5F-1	CpG island
ENSG00000201558	chromatin interactions
ENSG00000200913	chromatin interactions
ENSG00000222009	chromatin interactions
ENSG00000159592	chromatin interactions
ENSG00000202031	chromatin interactions
ENSG00000255946	chromatin interactions
ENSG00000132781	chromatin interactions
ENSG00000202444	chromatin interactions
ENSG00000100897	chromatin interactions
ENSG00000233396	chromatin interactions
ENSG00000129535	chromatin interactions
ENSG00000126107	chromatin interactions
ENSG00000187147	chromatin interactions
ENSG00000163636	chromatin interactions
ENSG00000188396	chromatin interactions
ENSG00000159596	chromatin interactions
ENSG00000142937	chromatin interactions
ENSG00000173846	chromatin interactions
ENSG00000126088	chromatin interactions
ENSG00000117425	chromatin interactions
ENSG00000101608	chromatin interactions
ENSG00000117450	chromatin interactions
ENSG00000132773	chromatin interactions

Extended variants
information (count: 94 )
Associated
traits (count: 89 )

Variant overlapped rSNPs/rCNVs (count:94 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs562574690	chr1:45189234-45189235	Weak transcription Flanking Active TSS Enhancers Active TSS	TF binding region Chromatin interactive region	20 gene(s)	Overlapped CNVs	n/a
2	rs187955642	chr1:45189238-45189239	Weak transcription Flanking Active TSS Enhancers Active TSS	TF binding region Chromatin interactive region	20 gene(s)	Overlapped CNVs	n/a
3	rs551282967	chr1:45189266-45189267	Weak transcription Flanking Active TSS Enhancers Active TSS	TF binding region Chromatin interactive region	20 gene(s)	Overlapped CNVs	n/a
4	rs571321906	chr1:45189284-45189285	Weak transcription Flanking Active TSS Enhancers Active TSS	TF binding region Chromatin interactive region	20 gene(s)	Overlapped CNVs	n/a
5	rs527492930	chr1:45189328-45189329	Weak transcription Flanking Active TSS Enhancers Active TSS	TF binding region Chromatin interactive region	18 gene(s)	Overlapped CNVs	n/a
6	rs548721047	chr1:45189336-45189337	Weak transcription Flanking Active TSS Enhancers Active TSS	TF binding region Chromatin interactive region	18 gene(s)	Overlapped CNVs	n/a
7	rs575614180	chr1:45189388-45189389	Weak transcription Flanking Active TSS Enhancers Active TSS	TF binding region Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
8	rs577567936	chr1:45189440-45189441	Weak transcription Flanking Active TSS Enhancers Bivalent/Poised TSS Active TSS	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
9	rs567354611	chr1:45189504-45189505	Weak transcription Flanking Active TSS Enhancers Bivalent/Poised TSS Active TSS	TF binding region Chromatin interactive region lncRNA	11 gene(s)	Overlapped CNVs	n/a
10	rs568596385	chr1:45189522-45189523	Weak transcription Flanking Active TSS Enhancers Bivalent/Poised TSS Active TSS	TF binding region Chromatin interactive region lncRNA	11 gene(s)	Overlapped CNVs	n/a
11	rs370624862	chr1:45189579-45189580	Weak transcription Flanking Active TSS Enhancers Bivalent/Poised TSS Active TSS	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
12	rs556180153	chr1:45189586-45189587	Weak transcription Flanking Active TSS Enhancers Bivalent/Poised TSS Active TSS	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
13	rs544394542	chr1:45189611-45189612	Weak transcription Genic enhancers Flanking Active TSS Enhancers Active TSS	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
14	rs538513163	chr1:45189630-45189631	Weak transcription Genic enhancers Flanking Active TSS Enhancers Active TSS	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
15	rs558436090	chr1:45189687-45189688	Weak transcription Genic enhancers Flanking Active TSS Enhancers Active TSS	TF binding region Chromatin interactive region lncRNA	10 gene(s)	Overlapped CNVs	n/a
16	rs544735608	chr1:45189744-45189745	Weak transcription Genic enhancers Flanking Active TSS Enhancers Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	Overlapped CNVs	n/a
17	rs182464303	chr1:45189748-45189749	Weak transcription Genic enhancers Flanking Active TSS Enhancers Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	Overlapped CNVs	n/a
18	rs540817051	chr1:45189762-45189763	Weak transcription Genic enhancers Flanking Active TSS Enhancers Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	Overlapped CNVs	n/a
19	rs554111946	chr1:45189765-45189766	Weak transcription Genic enhancers Flanking Active TSS Enhancers Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	Overlapped CNVs	n/a
20	rs563411984	chr1:45189784-45189785	Weak transcription Genic enhancers Flanking Active TSS Enhancers Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	Overlapped CNVs	n/a
21	rs573777475	chr1:45189788-45189789	Weak transcription Genic enhancers Flanking Active TSS Enhancers Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	Overlapped CNVs	n/a
22	rs542737828	chr1:45189807-45189808	Weak transcription Genic enhancers Flanking Active TSS Enhancers Active TSS	TF binding region Chromatin interactive region lncRNA	9 gene(s)	Overlapped CNVs	n/a
23	rs562513670	chr1:45189811-45189812	Weak transcription Genic enhancers Flanking Active TSS Enhancers Active TSS	TF binding region Chromatin interactive region lncRNA	9 gene(s)	Overlapped CNVs	n/a
24	rs75696348	chr1:45189817-45189818	Weak transcription Genic enhancers Flanking Active TSS Enhancers Active TSS	TF binding region Chromatin interactive region lncRNA	9 gene(s)	Overlapped CNVs	n/a
25	rs544864126	chr1:45189820-45189821	Weak transcription Genic enhancers Flanking Active TSS Enhancers Active TSS	TF binding region Chromatin interactive region lncRNA	9 gene(s)	Overlapped CNVs	n/a
26	rs565190051	chr1:45189838-45189839	Weak transcription Genic enhancers Flanking Active TSS Enhancers Active TSS	TF binding region Chromatin interactive region lncRNA	9 gene(s)	Overlapped CNVs	n/a
27	rs149200146	chr1:45189855-45189856	Weak transcription Genic enhancers Flanking Active TSS Enhancers Active TSS	TF binding region Chromatin interactive region lncRNA	9 gene(s)	Overlapped CNVs	n/a
28	rs547562733	chr1:45189856-45189857	Weak transcription Genic enhancers Flanking Active TSS Enhancers Active TSS	TF binding region Chromatin interactive region lncRNA	9 gene(s)	Overlapped CNVs	n/a
29	rs372851998	chr1:45189877-45189878	Weak transcription Genic enhancers Flanking Active TSS Enhancers Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	Overlapped CNVs	n/a
30	rs376130625	chr1:45189921-45189922	Weak transcription Genic enhancers Flanking Active TSS Enhancers Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	Overlapped CNVs	n/a
31	rs369915668	chr1:45189951-45189952	Weak transcription Genic enhancers Flanking Active TSS Enhancers Active TSS	TF binding region Chromatin interactive region lncRNA	9 gene(s)	Overlapped CNVs	n/a
32	rs529793074	chr1:45189975-45189976	Weak transcription Genic enhancers Flanking Active TSS Enhancers Active TSS	TF binding region Chromatin interactive region lncRNA	8 gene(s)	Overlapped CNVs	n/a
33	rs549924932	chr1:45190044-45190045	Weak transcription Genic enhancers Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
34	rs1135319	chr1:45190093-45190094	Weak transcription Genic enhancers Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	8 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs374549433	chr1:45190123-45190124	Weak transcription Genic enhancers Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
36	rs538640801	chr1:45190277-45190278	Weak transcription Genic enhancers Enhancers Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
37	rs561084606	chr1:45190279-45190280	Weak transcription Genic enhancers Enhancers Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
38	rs143381915	chr1:45190385-45190386	Weak transcription Genic enhancers Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
39	rs12740046	chr1:45190407-45190408	Weak transcription Genic enhancers Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
40	rs534258310	chr1:45190431-45190432	Weak transcription Genic enhancers Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
41	rs185415192	chr1:45190563-45190564	Weak transcription Genic enhancers Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
42	rs573916633	chr1:45190652-45190653	Weak transcription Genic enhancers Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
43	rs536311607	chr1:45190699-45190700	Weak transcription Genic enhancers Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
44	rs111547555	chr1:45190720-45190721	Weak transcription Genic enhancers Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
45	rs556250455	chr1:45190750-45190751	Weak transcription Genic enhancers Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
46	rs575984276	chr1:45190757-45190758	Weak transcription Genic enhancers Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
47	rs545385133	chr1:45190760-45190761	Weak transcription Genic enhancers Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
48	rs370156304	chr1:45190836-45190837	Weak transcription Enhancers Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
49	rs374716973	chr1:45190837-45190838	Weak transcription Enhancers Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
50	rs190381026	chr1:45190843-45190844	Weak transcription Enhancers Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:89)

Disease	PMID	Source
Acute lymphoblastic leukemia	20067559	CNVD
Melanoma	18172304	CNVD
Glioblastoma multiforme	21080181	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	17603634	CNVD
Soft tissue tumor	16732325	CNVD
Papillary thyroid carcinoma	21436994	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Colorectal cancer	16272173	CNVD
Wilms tumour	21544195	CNVD
Coronary Disease	20032323	CNVD
Prostate cancer	21965145	CNVD
Stargardt''s disease	17277736	CNVD
Neuroblastoma	17897457	CNVD
Uveal melanoma	21693616	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	21484798	CNVD
Non-syndromic sensorineural hearing loss	22290220	CNVD
Liposarcoma	21253554	CNVD
Breast cancer	21264507	CNVD
Acute myeloid leukemia	16864856	CNVD
Astrocytoma	17387387	CNVD
Cancer	21499728	CNVD
Glioblastoma multiforme	17387387	CNVD
Oligodendroglial tumors	17285580	CNVD
Neuroblastoma	17535989	CNVD
Pheochromocytoma	17535989	CNVD
Prostate cancer	16705090	CNVD
Astrocytoma	17934521	CNVD
Colorectal cancer	19359472	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Neuroblastoma	17533364	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Chronic myeloid leukemia	21384125	CNVD
Prostate cancer	18632612	CNVD
Autism	22495311	CNVD
Non-small cell lung cancer	21385341	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Chordoma	21602918	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Multiple myeloma	16461302	CNVD
Melanoma	17363583	CNVD
Cancer	21129771	CNVD
Autosomal dominant nocturnal frontal lobe epilepsy	18472482	CNVD
Hirschsprung''s Disease	21712996	CNVD
Non-small cell lung cancer	20864512	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Thrombocytopenia-absent radius syndrome	21933853	CNVD
Psychiatric disorder	22848183	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	20409316	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Lung cancer	18438408	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17393978	CNVD
Cervical cancer	21062161	CNVD
Cancer	21183584	CNVD
Uveal melanoma	20484589	CNVD
Ovarian cancer	22174824	CNVD
Muscle-eye-brain disease	21572526	CNVD
Breast cancer	21785460	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	21364760	CNVD
Breast cancer	20680643	CNVD
Colorectal cancer	19287155	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:152 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:45174400-45190400	Weak transcription	Lung	lung
2	chr1:45181200-45194800	Weak transcription	Brain Anterior Caudate	brain
3	chr1:45184000-45189200	Weak transcription	Sigmoid Colon	Sigmoid Colon
4	chr1:45184000-45191000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr1:45185200-45189200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
6	chr1:45185200-45190600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
7	chr1:45185200-45192400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
8	chr1:45185600-45192200	Weak transcription	NHDF-Ad	bronchial
9	chr1:45185600-45194800	Weak transcription	Dnd41	blood
10	chr1:45186000-45189600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
11	chr1:45186000-45190200	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
12	chr1:45186200-45192400	Weak transcription	HSMM	muscle
13	chr1:45187800-45189200	Enhancers	Primary T regulatory cells fromperipheralblood	blood
14	chr1:45187800-45189400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
15	chr1:45187800-45196200	Weak transcription	Right Atrium	heart
16	chr1:45188000-45189200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
17	chr1:45188000-45189400	Enhancers	K562	blood
18	chr1:45188000-45190800	Weak transcription	HUES6 Cell Line	embryonic stem cell
19	chr1:45188000-45191000	Weak transcription	HepG2	liver
20	chr1:45188000-45192400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
21	chr1:45188000-45192400	Weak transcription	Muscle Satellite Cultured Cells	--
22	chr1:45188000-45192400	Weak transcription	A549	lung
23	chr1:45188000-45192400	Weak transcription	Osteobl	bone
24	chr1:45188000-45195800	Weak transcription	H1 Cell Line	embryonic stem cell
25	chr1:45188200-45189400	Enhancers	Colonic Mucosa	Colon
26	chr1:45188200-45190800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
27	chr1:45188600-45190800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
28	chr1:45188600-45190800	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
29	chr1:45188800-45189400	Flanking Active TSS	Duodenum Mucosa	Duodenum
30	chr1:45188800-45189400	Flanking Active TSS	Thymus	Thymus
31	chr1:45188800-45189600	Flanking Active TSS	Primary T killer memory cells from peripheral blood	blood
32	chr1:45188800-45189600	Enhancers	Placenta	Placenta
33	chr1:45188800-45189600	Active TSS	Rectal Smooth Muscle	rectum
34	chr1:45188800-45189800	Flanking Active TSS	Primary B cells from cord blood	blood
35	chr1:45188800-45189800	Flanking Active TSS	Primary hematopoietic stem cells	blood
36	chr1:45188800-45189800	Flanking Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
37	chr1:45188800-45189800	Flanking Active TSS	Primary mononuclear cells fromperipheralblood	Blood
38	chr1:45188800-45189800	Enhancers	Liver	Liver
39	chr1:45188800-45189800	Active TSS	Rectal Mucosa Donor 29	rectum
40	chr1:45188800-45190000	Flanking Active TSS	Primary monocytes fromperipheralblood	blood
41	chr1:45188800-45190000	Flanking Active TSS	Primary T cells from cord blood	blood
42	chr1:45188800-45190000	Flanking Active TSS	Primary T cells fromperipheralblood	blood
43	chr1:45188800-45190000	Flanking Active TSS	Primary T helper 17 cells PMA-I stimulated	--
44	chr1:45188800-45190000	Flanking Active TSS	GM12878-XiMat	blood
45	chr1:45188800-45190200	Flanking Active TSS	Primary T helper naive cells fromperipheralblood	blood
46	chr1:45188800-45190200	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
47	chr1:45188800-45190200	Flanking Active TSS	Primary T killer naive cells fromperipheralblood	blood
48	chr1:45188800-45190600	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
49	chr1:45188800-45190800	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
50	chr1:45188800-45190800	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--

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