Variant report

Variant	esv3345981
Chromosome Location	chr1:247273879-247276577
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:351)
CpG islands
(count:915)
Chromatin interactive
region (count:12)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:351 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:247275900-247276723	HepG2	liver:	n/a	n/a
2	ARID3A	chr1:247273976-247274367	K562	blood:	n/a	n/a
3	ATF1	chr1:247273899-247274258	K562	blood:	n/a	n/a
4	BACH1	chr1:247275257-247275476	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr1:247275291-247275489	K562	blood:	n/a	n/a
6	BACH1	chr1:247274377-247274386	H1-hESC	embryonic stem cell:	n/a	n/a
7	BACH1	chr1:247274741-247274742	H1-hESC	embryonic stem cell:	n/a	n/a
8	BCLAF1	chr1:247273936-247274355	K562	blood:	n/a	n/a
9	BHLHE40	chr1:247275761-247275831	K562	blood:	n/a	n/a
10	BHLHE40	chr1:247274816-247275552	K562	blood:	n/a	n/a
11	BHLHE40	chr1:247276350-247276737	HepG2	liver:	n/a	n/a
12	BHLHE40	chr1:247273922-247274377	K562	blood:	n/a	n/a
13	BHLHE40	chr1:247274839-247275896	HepG2	liver:	n/a	chr1:247275614-247275630
14	BRCA1	chr1:247276484-247276640	HepG2	liver:	n/a	n/a
15	BRCA1	chr1:247275122-247275252	HepG2	liver:	n/a	n/a
16	BRCA1	chr1:247275738-247275926	HepG2	liver:	n/a	n/a
17	CBX3	chr1:247273868-247274371	K562	blood:	n/a	n/a
18	CBX3	chr1:247273762-247274572	K562	blood:	n/a	n/a
19	CBX3	chr1:247274963-247275912	K562	blood:	n/a	n/a
20	CCNT2	chr1:247273918-247275918	K562	blood:	n/a	n/a
21	CEBPB	chr1:247273913-247274328	K562	blood:	n/a	n/a
22	CEBPB	chr1:247274003-247274263	K562	blood:	n/a	n/a
23	CEBPD	chr1:247274982-247275541	HepG2	liver:	n/a	n/a
24	CEBPD	chr1:247276327-247276598	HepG2	liver:	n/a	n/a
25	CEBPD	chr1:247275082-247275591	K562	blood:	n/a	n/a
26	CEBPD	chr1:247273816-247274408	K562	blood:	n/a	n/a
27	CEBPD	chr1:247273827-247274410	K562	blood:	n/a	n/a
28	CHD1	chr1:247274697-247274777	H1-hESC	embryonic stem cell:	n/a	n/a
29	CHD2	chr1:247275082-247275678	HepG2	liver:	n/a	n/a
30	CHD2	chr1:247275222-247275495	K562	blood:	n/a	n/a
31	CHD2	chr1:247274611-247274669	K562	blood:	n/a	n/a
32	CHD2	chr1:247275334-247275404	H1-hESC	embryonic stem cell:	n/a	n/a
33	CHD2	chr1:247274012-247274212	K562	blood:	n/a	n/a
34	CTCF	chr1:247276477-247276543	HepG2	liver:	n/a	chr1:247276521-247276537 chr1:247276520-247276538 chr1:247276515-247276536
35	CTCF	chr1:247274980-247275130	WERI-Rb-1	eye:	n/a	n/a
36	CTCF	chr1:247276380-247276530	RPTEC	kidney:	n/a	n/a
37	CTCF	chr1:247274980-247275130	AG04449	skin:	n/a	n/a
38	CTCF	chr1:247276460-247276610	HepG2	liver:	n/a	chr1:247276521-247276537 chr1:247276520-247276538 chr1:247276515-247276536
39	CTCF	chr1:247276529-247276564	Gliobla	brain:	n/a	n/a
40	CUX1	chr1:247273995-247274540	K562	blood:	n/a	n/a
41	E2F6	chr1:247273892-247274249	K562	blood:	n/a	n/a
42	E2F6	chr1:247273891-247274152	K562	blood:	n/a	n/a
43	E2F6	chr1:247274248-247275874	K562	blood:	n/a	chr1:247275577-247275587 chr1:247275750-247275759
44	E2F6	chr1:247275000-247275587	A549	lung:	n/a	chr1:247275577-247275587
45	E2F6	chr1:247274556-247274925	K562	blood:	n/a	n/a
46	E2F6	chr1:247274949-247275662	A549	lung:	n/a	chr1:247275577-247275587
47	E2F6	chr1:247273922-247275849	K562	blood:	n/a	chr1:247275577-247275587 chr1:247275750-247275759
48	E2F6	chr1:247275037-247275388	K562	blood:	n/a	n/a
49	EGR1	chr1:247274423-247274837	K562	blood:	n/a	n/a
50	EGR1	chr1:247273902-247274307	K562	blood:	n/a	n/a

(count:915 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:247275872-247275922	GM06990	blood:	n/a
2	chr1:247275998-247276048	ProgFib	skin:	n/a
3	chr1:247275326-247275376	SK-N-MC	brain:	n/a
4	chr1:247275998-247276048	RPTEC	kidney:	n/a
5	chr1:247274454-247274504	NHDF-neo	bronchial:	n/a
6	chr1:247275469-247275519	HRE	kidney:	n/a
7	chr1:247275872-247275922	T-47D	breast:	n/a
8	chr1:247275542-247275592	HCF	heart:	n/a
9	chr1:247275872-247275922	H1-hESC	embryonic stem cell:	embryo
10	chr1:247275735-247275785	K562	blood:	n/a
11	chr1:247275735-247275785	AG09319	gingival:	n/a
12	chr1:247275542-247275592	Caco-2	colon:	n/a
13	chr1:247275469-247275519	BE2_C	brain:	n/a
14	chr1:247275326-247275376	HAEpiC	amniotic membrane:	n/a
15	chr1:247275735-247275785	HCPEpiC	choroid plexus:	n/a
16	chr1:247274709-247274759	SK-N-SH_RA	brain:	n/a
17	chr1:247274370-247274420	GM12892	blood:	n/a
18	chr1:247274777-247274827	ProgFib	skin:	n/a
19	chr1:247275808-247275858	AG04450	lung:	fetal
20	chr1:247274777-247274827	K562	blood:	n/a
21	chr1:247275872-247275922	HAEpiC	amniotic membrane:	n/a
22	chr1:247275872-247275922	MCF-7	breast:	n/a
23	chr1:247275808-247275858	ECC-1	luminal epithelium:	n/a
24	chr1:247274454-247274504	SAEC	small airway:	n/a
25	chr1:247275872-247275922	BE2_C	brain:	n/a
26	chr1:247274454-247274504	T-47D	breast:	n/a
27	chr1:247275344-247275394	AG09309	skin:	n/a
28	chr1:247275542-247275592	GM06990	blood:	n/a
29	chr1:247274454-247274504	K562	blood:	n/a
30	chr1:247275872-247275922	NHBE	bronchial:	n/a
31	chr1:247276096-247276146	AoSMC	blood vessel:	n/a
32	chr1:247274370-247274420	HL-60	blood:	n/a
33	chr1:247276096-247276146	PFSK-1	brain:	n/a
34	chr1:247275542-247275592	HL-60	blood:	n/a
35	chr1:247275542-247275592	Hepatocyte	liver:	n/a
36	chr1:247275469-247275519	AoSMC	blood vessel:	n/a
37	chr1:247275489-247275539	PFSK-1	brain:	n/a
38	chr1:247275872-247275922	SK-N-MC	brain:	n/a
39	chr1:247275998-247276048	BJ	skin:	n/a
40	chr1:247276096-247276146	ovcar-3	ovarian:	n/a
41	chr1:247275344-247275394	Caco-2	colon:	n/a
42	chr1:247274777-247274827	A549	lung:	n/a
43	chr1:247275542-247275592	HCT-116	colon:	n/a
44	chr1:247274777-247274827	IMR90	lung:	fetal
45	chr1:247274454-247274504	BJ	skin:	n/a
46	chr1:247274454-247274504	BE2_C	brain:	n/a
47	chr1:247275808-247275858	A549	lung:	n/a
48	chr1:247274777-247274827	GM06990	blood:	n/a
49	chr1:247275735-247275785	HRPEpiC	eye:	n/a
50	chr1:247275489-247275539	K562	blood:	n/a

(count:12 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:247261271..247263933-chr1:247276366..247278097,2	K562	blood:
2	chr1:247273239..247275061-chr1:247277041..247280302,3	K562	blood:
3	chr1:247241483..247244418-chr1:247273727..247276454,2	MCF-7	breast:
4	chr1:247092146..247096759-chr1:247274350..247278356,6	MCF-7	breast:
5	chr1:247274493..247276812-chr1:247371838..247375899,3	K562	blood:
6	chr1:247262370..247270931-chr1:247272613..247278774,19	MCF-7	breast:
7	chr1:247240305..247243596-chr1:247273338..247276480,4	K562	blood:
8	chr1:247236707..247239427-chr1:247272612..247275121,2	K562	blood:
9	chr1:247256992..247261249-chr1:247272069..247275489,5	K562	blood:
10	chr1:247271757..247273641-chr1:247273728..247275536,3	MCF-7	breast:
11	chr1:247276067..247278651-chr1:247493890..247496062,2	MCF-7	breast:
12	chr1:247275409..247277041-chr1:247418740..247421372,2	K562	blood:

No data

Variant related genes	Relation type
C1orf229	TF binding region
C1orf229	CpG island
ENSG00000197617	chromatin interactions
ENSG00000153207	chromatin interactions
ENSG00000188295	chromatin interactions
ENSG00000162714	chromatin interactions
ENSG00000227671	chromatin interactions
ENSG00000135747	chromatin interactions

Extended variants
information (count: 94 )
Associated
traits (count: 30 )

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	rs577800297	chr1:247273885-247273886	Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs201871095	chr1:247273890-247273891	Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs74163730	chr1:247273897-247273898	Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs533816806	chr1:247273902-247273903	Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs139504369	chr1:247273920-247273921	Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs375111634	chr1:247273976-247273977	Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs116304437	chr1:247274016-247274017	Flanking Bivalent TSS/Enh Bivalent/Poised TSS Enhancers Flanking Active TSS Active TSS Bivalent Enhancer Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs373161230	chr1:247274024-247274025	Flanking Bivalent TSS/Enh Bivalent/Poised TSS Enhancers Flanking Active TSS Active TSS Bivalent Enhancer Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs539567869	chr1:247274054-247274055	Flanking Bivalent TSS/Enh Bivalent/Poised TSS Enhancers Flanking Active TSS Active TSS Bivalent Enhancer Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs114913481	chr1:247274055-247274056	Flanking Bivalent TSS/Enh Bivalent/Poised TSS Enhancers Flanking Active TSS Active TSS Bivalent Enhancer Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs576015586	chr1:247274067-247274068	Flanking Bivalent TSS/Enh Bivalent/Poised TSS Enhancers Flanking Active TSS Active TSS Bivalent Enhancer Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs541812750	chr1:247274104-247274105	Flanking Bivalent TSS/Enh Bivalent/Poised TSS Enhancers Flanking Active TSS Active TSS Bivalent Enhancer Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs369902233	chr1:247274133-247274134	Flanking Bivalent TSS/Enh Bivalent/Poised TSS Enhancers Flanking Active TSS Active TSS Bivalent Enhancer Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs542484228	chr1:247274158-247274159	Flanking Bivalent TSS/Enh Bivalent/Poised TSS Enhancers Flanking Active TSS Active TSS Bivalent Enhancer Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs575095580	chr1:247274191-247274192	Flanking Bivalent TSS/Enh Bivalent/Poised TSS Enhancers Flanking Active TSS Active TSS Bivalent Enhancer Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs540511950	chr1:247274193-247274194	Flanking Bivalent TSS/Enh Bivalent/Poised TSS Enhancers Flanking Active TSS Active TSS Bivalent Enhancer Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs138275002	chr1:247274200-247274201	Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Enhancers Flanking Active TSS Active TSS Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs74152930	chr1:247274215-247274216	Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs552290535	chr1:247274293-247274294	Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs12140983	chr1:247274351-247274352	Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs531658373	chr1:247274354-247274355	Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs149613325	chr1:247274359-247274360	Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs568328177	chr1:247274379-247274380	Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs372844861	chr1:247274409-247274410	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs73135914	chr1:247274484-247274485	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs181391973	chr1:247274516-247274517	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Enhancers Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
27	rs539655573	chr1:247274527-247274528	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Enhancers Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
28	rs113338290	chr1:247274540-247274541	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Enhancers Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
29	rs556349106	chr1:247274575-247274576	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Enhancers Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
30	rs569755137	chr1:247274576-247274577	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Enhancers Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
31	rs547457449	chr1:247274588-247274589	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Enhancers Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
32	rs114948365	chr1:247274638-247274639	Bivalent/Poised TSS Active TSS Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
33	rs12031553	chr1:247274701-247274702	Bivalent/Poised TSS Active TSS Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
34	rs571928030	chr1:247274740-247274741	Bivalent/Poised TSS Active TSS Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
35	rs540573120	chr1:247274753-247274754	Bivalent/Poised TSS Active TSS Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
36	rs554036898	chr1:247274770-247274771	Bivalent/Poised TSS Active TSS Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
37	rs143099468	chr1:247274839-247274840	Bivalent/Poised TSS Active TSS Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
38	rs545987988	chr1:247274854-247274855	Bivalent/Poised TSS Active TSS Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
39	rs562909507	chr1:247274861-247274862	Bivalent/Poised TSS Active TSS Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
40	rs531848129	chr1:247274873-247274874	Bivalent/Poised TSS Active TSS Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
41	rs369865565	chr1:247274883-247274884	Bivalent/Poised TSS Active TSS Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
42	rs73135916	chr1:247274899-247274900	Bivalent/Poised TSS Active TSS Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
43	rs562139376	chr1:247274987-247274988	Bivalent/Poised TSS Active TSS Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
44	rs527682577	chr1:247275000-247275001	Bivalent/Poised TSS Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
45	rs551464466	chr1:247275013-247275014	Bivalent/Poised TSS Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
46	rs547773966	chr1:247275054-247275055	Bivalent/Poised TSS Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
47	rs570763569	chr1:247275068-247275069	Bivalent/Poised TSS Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
48	rs533235929	chr1:247275083-247275084	Bivalent/Poised TSS Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
49	rs377558360	chr1:247275091-247275092	Bivalent/Poised TSS Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
50	rs549965032	chr1:247275208-247275209	Bivalent/Poised TSS Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:30)

Disease	PMID	Source
Breast cancer	17133270	CNVD
Acute lymphoblastic leukemia	20435627	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
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17001317	CNVD
Neuroblastoma	18923191	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Breast cancer	21509527	CNVD
Hepatocellular carcinoma	18803288	CNVD
Urothelial tumor	18831757	CNVD
Basal cell lymphoma	17170743	CNVD
Basal cell lymphoma	17053054	CNVD
Cancer	17060936	CNVD
Multiple myeloma	16616336	CNVD
Cutaneous malignant melanoma	18794153	CNVD
Astrocytoma	17934521	CNVD
Neurocytoma	17123091	CNVD
Central neurocytomas	17123091	CNVD
Breast cancer	20409316	CNVD
Fibroblasts	17951408	CNVD
Lung cancer	17951408	CNVD

Chromatin state (count:450 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:247268400-247274000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
2	chr1:247268400-247274000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
3	chr1:247268400-247274000	Weak transcription	Fetal Brain Female	brain
4	chr1:247268400-247275600	Weak transcription	Fetal Heart	heart
5	chr1:247268600-247274000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
6	chr1:247268600-247274000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
7	chr1:247268600-247274000	Weak transcription	Brain Angular Gyrus	brain
8	chr1:247268600-247274000	Weak transcription	Brain Cingulate Gyrus	brain
9	chr1:247268600-247274000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
10	chr1:247268600-247274000	Weak transcription	Duodenum Smooth Muscle	Duodenum
11	chr1:247268600-247274000	Weak transcription	Right Atrium	heart
12	chr1:247268600-247274000	Weak transcription	NH-A	brain
13	chr1:247268600-247274000	Weak transcription	NHDF-Ad	bronchial
14	chr1:247268600-247274200	Weak transcription	Right Ventricle	heart
15	chr1:247268800-247274000	Weak transcription	Brain Hippocampus Middle	brain
16	chr1:247268800-247274000	Weak transcription	Colonic Mucosa	Colon
17	chr1:247268800-247274000	Weak transcription	Ovary	ovary
18	chr1:247268800-247274000	Weak transcription	Skeletal Muscle Male	skeletal muscle
19	chr1:247268800-247274000	Weak transcription	Stomach Smooth Muscle	stomach
20	chr1:247268800-247274000	Weak transcription	HepG2	liver
21	chr1:247268800-247274000	Weak transcription	Osteobl	bone
22	chr1:247269000-247274000	Weak transcription	H9 Cell Line	embryonic stem cell
23	chr1:247271200-247274000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
24	chr1:247271400-247274000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
25	chr1:247272200-247274000	Weak transcription	Brain Substantia Nigra	brain
26	chr1:247273000-247274000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
27	chr1:247273000-247274000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
28	chr1:247273400-247274000	Enhancers	Fetal Muscle Leg	muscle
29	chr1:247273600-247274000	Enhancers	Fetal Muscle Trunk	muscle
30	chr1:247273800-247274000	Bivalent Enhancer	Primary hematopoietic stem cells	blood
31	chr1:247273800-247274000	Bivalent Enhancer	Primary T helper naive cells fromperipheralblood	blood
32	chr1:247273800-247274000	Bivalent/Poised TSS	Primary T helper memory cells from peripheral blood 1	blood
33	chr1:247273800-247274000	Bivalent Enhancer	Primary T helper cells PMA-I stimulated	--
34	chr1:247273800-247274000	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
35	chr1:247273800-247274000	Bivalent Enhancer	Primary T helper cells fromperipheralblood	blood
36	chr1:247273800-247274000	Bivalent Enhancer	Primary T killer memory cells from peripheral blood	blood
37	chr1:247273800-247274000	Enhancers	Cortex derived primary cultured neurospheres	brain
38	chr1:247273800-247274000	Enhancers	Adipose Nuclei	Adipose
39	chr1:247273800-247274000	Enhancers	Colon Smooth Muscle	Colon
40	chr1:247273800-247274000	Weak transcription	Esophagus	oesophagus
41	chr1:247273800-247274000	Enhancers	Fetal Lung	lung
42	chr1:247273800-247274000	Bivalent Enhancer	Fetal Stomach	stomach
43	chr1:247273800-247274000	Enhancers	Psoas Muscle	Psoas
44	chr1:247273800-247274000	Active TSS	Rectal Mucosa Donor 29	rectum
45	chr1:247273800-247274000	Enhancers	Rectal Mucosa Donor 31	rectum
46	chr1:247273800-247274000	Enhancers	Skeletal Muscle Female	skeletal muscle
47	chr1:247273800-247274200	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
48	chr1:247273800-247274200	Bivalent Enhancer	Primary B cells from peripheral blood	blood
49	chr1:247273800-247274200	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
50	chr1:247273800-247274200	Bivalent Enhancer	Primary Natural Killer cells fromperipheralblood	blood

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