Variant report

Variant	esv3438872
Chromosome Location	chr4:8237102-8239900
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:73)
CpG islands
(count:183)
Chromatin interactive
region (count:10)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:73 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CEBPB	chr4:8239710-8239910	H1-hESC	embryonic stem cell:	n/a	chr4:8239801-8239812
2	CEBPB	chr4:8239686-8239976	IMR90	lung:	n/a	chr4:8239801-8239812
3	CEBPB	chr4:8239726-8239919	K562	blood:	n/a	chr4:8239801-8239812
4	CEBPB	chr4:8239639-8239992	Hela-S3	cervix:	n/a	chr4:8239801-8239812
5	CEBPB	chr4:8239678-8239982	HepG2	liver:	n/a	chr4:8239801-8239812
6	CTCF	chr4:8237964-8238095	MCF-7	breast:	n/a	n/a
7	CTCF	chr4:8237888-8238204	K562	blood:	n/a	n/a
8	CTCF	chr4:8237928-8238157	K562	blood:	n/a	n/a
9	CTCF	chr4:8237928-8238131	K562	blood:	n/a	n/a
10	CTCF	chr4:8238260-8238410	SK-N-SH_RA	brain:	n/a	n/a
11	CTCF	chr4:8237981-8238087	MCF-7	breast:	n/a	n/a
12	CTCF	chr4:8237940-8238090	K562	blood:	n/a	n/a
13	CTCF	chr4:8237981-8238108	MCF-7	breast:	n/a	n/a
14	CTCF	chr4:8237955-8238112	H1-hESC	embryonic stem cell:	n/a	n/a
15	CTCF	chr4:8237976-8238118	Medullo	brain:	n/a	n/a
16	CTCF	chr4:8237779-8238290	K562	blood:	n/a	n/a
17	CTCF	chr4:8237833-8238223	K562	blood:	n/a	n/a
18	CUX1	chr4:8239772-8239861	K562	blood:	n/a	n/a
19	FOS	chr4:8239763-8239912	MCF10A-Er-Src	breast:	n/a	n/a
20	GTF2F1	chr4:8239795-8239915	Hela-S3	cervix:	n/a	n/a
21	JUND	chr4:8239262-8239462	HepG2	liver:	n/a	n/a
22	MAX	chr4:8239781-8240167	MCF-7	breast:	n/a	n/a
23	MAX	chr4:8237916-8237966	NB4	blood:	n/a	chr4:8237923-8237933
24	MAZ	chr4:8237955-8238130	K562	blood:	n/a	n/a
25	MXI1	chr4:8238068-8238742	SK-N-SH	brain:	n/a	n/a
26	MYC	chr4:8239813-8240009	MCF10A-Er-Src	breast:	n/a	n/a
27	POLR2A	chr4:8238730-8238797	HepG2	liver:	n/a	n/a
28	POLR2A	chr4:8235870-8237849	GM12878	blood:	n/a	n/a
29	POLR2A	chr4:8239456-8239470	HUVEC	blood vessel:	n/a	n/a
30	POLR2A	chr4:8237066-8237131	A549	lung:	n/a	n/a
31	POLR2A	chr4:8237390-8237753	HUVEC	blood vessel:	n/a	n/a
32	POLR2A	chr4:8236593-8237501	HepG2	liver:	n/a	n/a
33	POLR2A	chr4:8239077-8239204	GM12878	blood:	n/a	n/a
34	POLR2A	chr4:8238070-8238765	GM12878	blood:	n/a	n/a
35	POLR2A	chr4:8237455-8237464	GM12878	blood:	n/a	n/a
36	POLR2A	chr4:8237273-8237287	HUVEC	blood vessel:	n/a	n/a
37	POLR2A	chr4:8236666-8237224	HUVEC	blood vessel:	n/a	n/a
38	POLR2A	chr4:8239247-8239354	HepG2	liver:	n/a	n/a
39	POLR2A	chr4:8237556-8237583	HUVEC	blood vessel:	n/a	n/a
40	POLR2A	chr4:8239376-8239390	HUVEC	blood vessel:	n/a	n/a
41	POLR2A	chr4:8237123-8237987	PFSK-1	brain:	n/a	n/a
42	POLR2A	chr4:8237845-8238093	GM12878	blood:	n/a	n/a
43	POLR2A	chr4:8239802-8241426	HepG2	liver:	n/a	n/a
44	POLR2A	chr4:8238753-8239114	HUVEC	blood vessel:	n/a	n/a
45	POLR2A	chr4:8237329-8237428	HUVEC	blood vessel:	n/a	n/a
46	POLR2A	chr4:8238544-8238785	GM12878	blood:	n/a	n/a
47	POLR2A	chr4:8239858-8240169	HepG2	liver:	n/a	n/a
48	POLR2A	chr4:8237472-8237508	HUVEC	blood vessel:	n/a	n/a
49	POLR2A	chr4:8236693-8237262	GM12892	blood:	n/a	n/a
50	POLR2A	chr4:8236083-8237232	K562	blood:	n/a	n/a

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:8239254-8239304	NB4	blood:	n/a
2	chr4:8239254-8239304	Hepatocyte	liver:	n/a
3	chr4:8239220-8239270	AG10803	skin:	n/a
4	chr4:8239254-8239304	HRCEpiC	kidney:	n/a
5	chr4:8239303-8239353	HEEpiC	esophagus:	n/a
6	chr4:8239303-8239353	HRCEpiC	kidney:	n/a
7	chr4:8239220-8239270	ProgFib	skin:	n/a
8	chr4:8239303-8239353	BJ	skin:	n/a
9	chr4:8239303-8239353	HUVEC	blood vessel:	n/a
10	chr4:8239254-8239304	HepG2	liver:	n/a
11	chr4:8239220-8239270	HL-60	blood:	n/a
12	chr4:8239303-8239353	HNPCEpiC	eye:	n/a
13	chr4:8239303-8239353	A549	lung:	n/a
14	chr4:8239254-8239304	HUVEC	blood vessel:	n/a
15	chr4:8239303-8239353	MCF-7	breast:	n/a
16	chr4:8239220-8239270	CMK	blood:	n/a
17	chr4:8239220-8239270	Caco-2	colon:	n/a
18	chr4:8239254-8239304	HEEpiC	esophagus:	n/a
19	chr4:8239254-8239304	HCF	heart:	n/a
20	chr4:8239220-8239270	HNPCEpiC	eye:	n/a
21	chr4:8239303-8239353	HPAEpiC	pulmonary alveolar:	n/a
22	chr4:8239254-8239304	Jurkat	blood:	n/a
23	chr4:8239303-8239353	PANC-1	pancreas:	n/a
24	chr4:8239220-8239270	HRCEpiC	kidney:	n/a
25	chr4:8239220-8239270	HCM	heart:	n/a
26	chr4:8239254-8239304	CMK	blood:	n/a
27	chr4:8239254-8239304	PANC-1	pancreas:	n/a
28	chr4:8239220-8239270	SK-N-SH_RA	brain:	n/a
29	chr4:8239254-8239304	MCF-7	breast:	n/a
30	chr4:8239254-8239304	NH-A	brain:	n/a
31	chr4:8239254-8239304	SK-N-MC	brain:	n/a
32	chr4:8239254-8239304	AG10803	skin:	n/a
33	chr4:8239254-8239304	BE2_C	brain:	n/a
34	chr4:8239254-8239304	SK-N-SH_RA	brain:	n/a
35	chr4:8239303-8239353	Hela-S3	cervix:	n/a
36	chr4:8239254-8239304	HIPEpiC	eye:	n/a
37	chr4:8239254-8239304	HAEpiC	amniotic membrane:	n/a
38	chr4:8239303-8239353	SKMC	muscle:	n/a
39	chr4:8239254-8239304	MCF10A-Er-Src	breast:	n/a
40	chr4:8239254-8239304	GM12878	blood:	n/a
41	chr4:8239303-8239353	HEK293	kidney:	embryo
42	chr4:8239303-8239353	U87	brain:	n/a
43	chr4:8239303-8239353	GM19239	blood:	n/a
44	chr4:8239303-8239353	MCF10A-Er-Src	breast:	n/a
45	chr4:8239220-8239270	Hepatocyte	liver:	n/a
46	chr4:8239220-8239270	HIPEpiC	eye:	n/a
47	chr4:8239220-8239270	U87	brain:	n/a
48	chr4:8239254-8239304	AoSMC	blood vessel:	n/a
49	chr4:8239303-8239353	Caco-2	colon:	n/a
50	chr4:8239220-8239270	HAEpiC	amniotic membrane:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr4:8178131..8179114-chr4:8239846..8240964,9	MCF-7	breast:
2	chr4:8195725..8198126-chr4:8238876..8240631,2	MCF-7	breast:
3	chr4:8178298..8179365-chr4:8239616..8240695,4	MCF-7	breast:
4	chr4:8233606..8235264-chr4:8235764..8238250,2	MCF-7	breast:
5	chr4:8201531..8203736-chr4:8237028..8240221,3	MCF-7	breast:
6	chr4:8183544..8186316-chr4:8238695..8241218,2	MCF-7	breast:
7	chr4:8178683..8179355-chr4:8239861..8240827,2	K562	blood:
8	chr4:8236579..8238924-chr4:8243496..8245332,2	K562	blood:
9	chr4:8238966..8241301-chr4:8261569..8263591,2	MCF-7	breast:
10	chr4:8230516..8235728-chr4:8236550..8239148,4	MCF-7	breast:

No data

Variant related genes	Relation type
SH3TC1	TF binding region
SH3TC1	CpG island
ENSG00000125089	chromatin interactions

Extended variants
information (count: 218 )
Associated
traits (count: 54 )

Variant overlapped rSNPs/rCNVs (count:218 , 50 per page) page: 1 2 3 4 5

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs370331531	chr4:8237108-8237109	Strong transcription Weak transcription Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs370799486	chr4:8237109-8237110	Strong transcription Weak transcription Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs375612788	chr4:8237124-8237125	Strong transcription Weak transcription Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs199612522	chr4:8237126-8237127	Strong transcription Weak transcription Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs554581794	chr4:8237153-8237154	Strong transcription Weak transcription Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs368354347	chr4:8237174-8237175	Strong transcription Weak transcription Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs372744255	chr4:8237189-8237190	Strong transcription Weak transcription Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs377306484	chr4:8237215-8237216	Strong transcription Genic enhancers Weak transcription Bivalent Enhancer Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs141656771	chr4:8237216-8237217	Strong transcription Genic enhancers Weak transcription Bivalent Enhancer Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs201366758	chr4:8237221-8237222	Strong transcription Genic enhancers Weak transcription Bivalent Enhancer Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs116197207	chr4:8237222-8237223	Strong transcription Genic enhancers Weak transcription Bivalent Enhancer Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs140996511	chr4:8237233-8237234	Strong transcription Genic enhancers Weak transcription Bivalent Enhancer Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs146468350	chr4:8237240-8237241	Strong transcription Genic enhancers Weak transcription Bivalent Enhancer Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs57688695	chr4:8237255-8237256	Strong transcription Genic enhancers Weak transcription Bivalent Enhancer Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs147031511	chr4:8237256-8237257	Strong transcription Genic enhancers Weak transcription Bivalent Enhancer Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs555747393	chr4:8237268-8237269	Strong transcription Genic enhancers Weak transcription Bivalent Enhancer Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs201857215	chr4:8237273-8237274	Strong transcription Genic enhancers Weak transcription Bivalent Enhancer Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs574770936	chr4:8237280-8237281	Strong transcription Genic enhancers Weak transcription Bivalent Enhancer Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs374013419	chr4:8237281-8237282	Strong transcription Genic enhancers Weak transcription Bivalent Enhancer Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs376169474	chr4:8237306-8237307	Strong transcription Genic enhancers Weak transcription Bivalent Enhancer Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs533008310	chr4:8237318-8237319	Strong transcription Genic enhancers Weak transcription Bivalent Enhancer Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs200192489	chr4:8237320-8237321	Strong transcription Genic enhancers Weak transcription Bivalent Enhancer Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs369971727	chr4:8237321-8237322	Strong transcription Genic enhancers Weak transcription Bivalent Enhancer Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs552543002	chr4:8237325-8237326	Strong transcription Genic enhancers Weak transcription Bivalent Enhancer Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs564417489	chr4:8237359-8237360	Strong transcription Genic enhancers Weak transcription Bivalent Enhancer Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs528624816	chr4:8237368-8237369	Strong transcription Genic enhancers Weak transcription Bivalent Enhancer Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs547258228	chr4:8237370-8237371	Strong transcription Genic enhancers Weak transcription Bivalent Enhancer Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs565893676	chr4:8237383-8237384	Strong transcription Genic enhancers Weak transcription Bivalent Enhancer Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs536472060	chr4:8237385-8237386	Strong transcription Genic enhancers Weak transcription Bivalent Enhancer Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs548470846	chr4:8237386-8237387	Strong transcription Genic enhancers Weak transcription Bivalent Enhancer Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs569975020	chr4:8237387-8237388	Strong transcription Genic enhancers Weak transcription Bivalent Enhancer Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs537041173	chr4:8237419-8237420	Strong transcription Genic enhancers Weak transcription Bivalent Enhancer Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs207464254	chr4:8237422-8237423	Strong transcription Genic enhancers Weak transcription Bivalent Enhancer Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs193036743	chr4:8237423-8237424	Strong transcription Genic enhancers Weak transcription Bivalent Enhancer Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs558563500	chr4:8237425-8237426	Strong transcription Genic enhancers Weak transcription Bivalent Enhancer Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs185733719	chr4:8237433-8237434	Strong transcription Genic enhancers Weak transcription Bivalent Enhancer Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs370541301	chr4:8237445-8237446	Strong transcription Genic enhancers Weak transcription Bivalent Enhancer Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs372805129	chr4:8237448-8237449	Strong transcription Genic enhancers Weak transcription Bivalent Enhancer Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs145892287	chr4:8237451-8237452	Strong transcription Genic enhancers Weak transcription Bivalent Enhancer Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs547919964	chr4:8237472-8237473	Strong transcription Genic enhancers Weak transcription Bivalent Enhancer Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs552817094	chr4:8237497-8237498	Strong transcription Genic enhancers Weak transcription Bivalent Enhancer Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs574660180	chr4:8237508-8237509	Strong transcription Genic enhancers Weak transcription Bivalent Enhancer Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs138616312	chr4:8237585-8237586	Strong transcription Genic enhancers Weak transcription Bivalent Enhancer Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs562939382	chr4:8237607-8237608	Strong transcription Genic enhancers Weak transcription Bivalent Enhancer Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs575576598	chr4:8237619-8237620	Strong transcription Genic enhancers Weak transcription Bivalent Enhancer Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs55848134	chr4:8237649-8237650	Strong transcription Genic enhancers Weak transcription Bivalent Enhancer Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs545865874	chr4:8237655-8237656	Strong transcription Genic enhancers Weak transcription Bivalent Enhancer Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs564537758	chr4:8237668-8237669	Strong transcription Genic enhancers Weak transcription Bivalent Enhancer Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs528554335	chr4:8237685-8237686	Strong transcription Genic enhancers Weak transcription Bivalent Enhancer Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs376468076	chr4:8237701-8237702	Strong transcription Genic enhancers Weak transcription Bivalent Enhancer Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:54)

Disease	PMID	Source
Wilms tumour	21544195	CNVD
Melanoma	20688739	CNVD
Colorectal cancer	16272173	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17603634	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Colorectal cancer	19359472	CNVD
Neuroblastoma	17533364	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Cancer	21637783	CNVD
Melanoma	21693616	CNVD
Squamous cell cancer	21044232	CNVD
Colorectal cancer	20709793	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Non-small cell lung cancer	21044232	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	17387387	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Cervical cancer	21062161	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Glioblastoma multiforme	21080181	CNVD
Chordoma	21602918	CNVD
HIV/AIDS	22032296	CNVD
Neuroblastoma	18923191	CNVD
small cell lung cancer	20016488	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Prostate cancer	18632612	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Breast cancer	21785460	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Breast cancer	21509527	CNVD
Lung cancer	18438408	CNVD
Urothelial carcinoma	21177765	CNVD
Myelofibrosis	22110671	CNVD
Hirschsprung''s Disease	21712996	CNVD
Schizophrenia	22241247	CNVD
Autosomal-dominant microtia	18179897	CNVD
Glioma	17123091	CNVD
Colorectal cancer	20459617	CNVD
Breast cancer	17133270	CNVD
Sezary syndrome	18413736	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Oligozoospermia	20877625	CNVD

Chromatin state (count:158 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:8228400-8240400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
2	chr4:8228400-8240800	Weak transcription	H9 Cell Line	embryonic stem cell
3	chr4:8228400-8243800	Weak transcription	Duodenum Smooth Muscle	Duodenum
4	chr4:8228800-8244200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr4:8230600-8239400	Strong transcription	Fetal Intestine Small	intestine
6	chr4:8230600-8243800	Weak transcription	Colon Smooth Muscle	Colon
7	chr4:8230800-8237200	Weak transcription	Ovary	ovary
8	chr4:8230800-8238000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
9	chr4:8230800-8240400	Weak transcription	Placenta Amnion	Placenta Amnion
10	chr4:8230800-8242800	Weak transcription	NHLF	lung
11	chr4:8230800-8244200	Weak transcription	Brain Cingulate Gyrus	brain
12	chr4:8230800-8244200	Weak transcription	Left Ventricle	heart
13	chr4:8230800-8244200	Weak transcription	Right Atrium	heart
14	chr4:8231000-8239600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
15	chr4:8231000-8241000	Strong transcription	Monocytes-CD14+_RO01746	blood
16	chr4:8231000-8243800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
17	chr4:8231000-8243800	Weak transcription	Brain Angular Gyrus	brain
18	chr4:8231200-8239800	Weak transcription	A549	lung
19	chr4:8231400-8237800	Strong transcription	Primary hematopoietic stem cells short term culture	blood
20	chr4:8232000-8243600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
21	chr4:8232200-8244200	Strong transcription	HUVEC	blood vessel
22	chr4:8232400-8241400	Strong transcription	Primary monocytes fromperipheralblood	blood
23	chr4:8232600-8239200	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
24	chr4:8232600-8240000	Strong transcription	Placenta	Placenta
25	chr4:8232800-8239400	Strong transcription	Fetal Intestine Large	intestine
26	chr4:8232800-8241800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
27	chr4:8232800-8242000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
28	chr4:8232800-8243800	Strong transcription	Lung	lung
29	chr4:8232800-8244200	Strong transcription	HMEC	breast
30	chr4:8233000-8237600	Strong transcription	Breast Myoepithelial Primary Cells	Breast
31	chr4:8233000-8240200	Strong transcription	Gastric	stomach
32	chr4:8233000-8243400	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
33	chr4:8233000-8243800	Strong transcription	Liver	Liver
34	chr4:8233000-8244000	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
35	chr4:8233200-8243800	Strong transcription	Fetal Stomach	stomach
36	chr4:8233600-8237600	Genic enhancers	Fetal Thymus	thymus
37	chr4:8233800-8238000	Strong transcription	Primary hematopoietic stem cells	blood
38	chr4:8233800-8239400	Strong transcription	Spleen	Spleen
39	chr4:8234000-8237200	Strong transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
40	chr4:8234000-8237400	Strong transcription	NHEK	skin
41	chr4:8234000-8239400	Strong transcription	Esophagus	oesophagus
42	chr4:8234000-8241800	Strong transcription	Adipose Nuclei	Adipose
43	chr4:8234000-8243200	Strong transcription	Pancreas	Pancrea
44	chr4:8234200-8237200	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
45	chr4:8234200-8239600	Strong transcription	Primary T helper cells PMA-I stimulated	--
46	chr4:8234200-8240400	Strong transcription	Duodenum Mucosa	Duodenum
47	chr4:8234200-8241600	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--
48	chr4:8234200-8243800	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
49	chr4:8234400-8239400	Weak transcription	Fetal Brain Male	brain
50	chr4:8234400-8243400	Strong transcription	Right Ventricle	heart

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