Variant report

Variant	esv3387612
Chromosome Location	chr4:715777-718325
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:61)
CpG islands
(count:427)
Chromatin interactive
region (count:7)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:61 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BCL3	chr4:716688-717009	GM12878	blood:	n/a	n/a
2	BCL3	chr4:716063-716428	GM12878	blood:	n/a	n/a
3	BCL3	chr4:716760-717113	GM12878	blood:	n/a	n/a
4	CTCF	chr4:718070-718260	HepG2	liver:	n/a	chr4:718218-718231
5	CTCF	chr4:718100-718250	HepG2	liver:	n/a	chr4:718218-718231
6	CTCF	chr4:718080-718230	HepG2	liver:	n/a	n/a
7	CTCF	chr4:716661-716711	Spleen_OC	spleen:	n/a	n/a
8	EGR1	chr4:715488-715873	K562	blood:	n/a	n/a
9	FOXA1	chr4:718062-718383	HepG2	liver:	n/a	chr4:718280-718292
10	FOXA1	chr4:718108-718388	HepG2	liver:	n/a	chr4:718280-718292
11	GABPA	chr4:716524-716766	GM12878	blood:	n/a	n/a
12	HNF4A	chr4:718121-718391	HepG2	liver:	n/a	chr4:718264-718279 chr4:718264-718279 chr4:718264-718279 chr4:718264-718279 chr4:718264-718279
13	HNF4A	chr4:718092-718313	HepG2	liver:	n/a	chr4:718264-718279 chr4:718264-718279 chr4:718264-718279 chr4:718264-718279 chr4:718264-718279
14	MAZ	chr4:718187-718285	HepG2	liver:	n/a	n/a
15	MXI1	chr4:718191-718202	HepG2	liver:	n/a	n/a
16	MYC	chr4:716392-716626	MCF-7	breast:	n/a	n/a
17	PAX5	chr4:716458-716837	GM12878	blood:	n/a	n/a
18	PBX3	chr4:716495-716773	GM12878	blood:	n/a	n/a
19	PBX3	chr4:716246-716974	GM12878	blood:	n/a	n/a
20	POLR2A	chr4:717567-717679	K562	blood:	n/a	n/a
21	POLR2A	chr4:715599-715896	K562	blood:	n/a	n/a
22	POLR2A	chr4:716431-716907	GM12878	blood:	n/a	n/a
23	POLR2A	chr4:716499-716873	GM12891	blood:	n/a	n/a
24	POLR2A	chr4:716311-716971	GM12891	blood:	n/a	n/a
25	POLR2A	chr4:717916-718163	GM12878	blood:	n/a	n/a
26	POLR2A	chr4:716255-716324	MCF-7	breast:	n/a	n/a
27	POLR2A	chr4:717930-718016	HepG2	liver:	n/a	n/a
28	POLR2A	chr4:717686-717688	K562	blood:	n/a	n/a
29	POLR2A	chr4:716469-716771	A549	lung:	n/a	n/a
30	POLR2A	chr4:717614-717832	GM12878	blood:	n/a	n/a
31	POLR2A	chr4:717546-717879	GM12892	blood:	n/a	n/a
32	POLR2A	chr4:717045-718006	SK-N-MC	brain:	n/a	n/a
33	POLR2A	chr4:715800-715882	GM12878	blood:	n/a	n/a
34	POLR2A	chr4:716243-717022	GM12878	blood:	n/a	n/a
35	POLR2A	chr4:716348-716993	GM12892	blood:	n/a	n/a
36	POLR2A	chr4:716796-716962	A549	lung:	n/a	n/a
37	POLR2A	chr4:717543-717594	K562	blood:	n/a	n/a
38	POLR2A	chr4:718175-718229	H1-hESC	embryonic stem cell:	n/a	n/a
39	POLR2A	chr4:715755-715944	HepG2	liver:	n/a	n/a
40	POLR2A	chr4:716335-716915	GM12891	blood:	n/a	n/a
41	POLR2A	chr4:717920-718343	GM12878	blood:	n/a	n/a
42	POLR2A	chr4:716472-716744	A549	lung:	n/a	n/a
43	POLR2A	chr4:716340-717023	GM12892	blood:	n/a	n/a
44	POLR2A	chr4:716396-716894	H1-hESC	embryonic stem cell:	n/a	n/a
45	POLR2A	chr4:716244-717062	GM12878	blood:	n/a	n/a
46	POLR2A	chr4:716249-716254	MCF-7	breast:	n/a	n/a
47	POLR2A	chr4:716205-716937	GM12878	blood:	n/a	n/a
48	POU2F2	chr4:716435-716943	GM12891	blood:	n/a	n/a
49	POU2F2	chr4:716438-716978	GM12891	blood:	n/a	n/a
50	RAD21	chr4:718019-718362	HepG2	liver:	n/a	n/a

(count:427 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:716883-716933	H1-hESC	embryonic stem cell:	embryo
2	chr4:715950-716000	NB4	blood:	n/a
3	chr4:716282-716332	HRCEpiC	kidney:	n/a
4	chr4:715865-715915	HepG2	liver:	n/a
5	chr4:715872-715922	ovcar-3	ovarian:	n/a
6	chr4:715872-715922	HRCEpiC	kidney:	n/a
7	chr4:716657-716707	Hepatocyte	liver:	n/a
8	chr4:716282-716332	Jurkat	blood:	n/a
9	chr4:716883-716933	Hepatocyte	liver:	n/a
10	chr4:716883-716933	NH-A	brain:	n/a
11	chr4:715872-715922	AoSMC	blood vessel:	n/a
12	chr4:715872-715922	Hepatocyte	liver:	n/a
13	chr4:716657-716707	HIPEpiC	eye:	n/a
14	chr4:717040-717090	GM12892	blood:	n/a
15	chr4:716657-716707	SAEC	small airway:	n/a
16	chr4:716883-716933	SAEC	small airway:	n/a
17	chr4:716657-716707	ovcar-3	ovarian:	n/a
18	chr4:716282-716332	MCF-7	breast:	n/a
19	chr4:717040-717090	HIPEpiC	eye:	n/a
20	chr4:715872-715922	HIPEpiC	eye:	n/a
21	chr4:715950-716000	Caco-2	colon:	n/a
22	chr4:716282-716332	HCPEpiC	choroid plexus:	n/a
23	chr4:715872-715922	Hela-S3	cervix:	n/a
24	chr4:716657-716707	HPAEpiC	pulmonary alveolar:	n/a
25	chr4:717040-717090	HCF	heart:	n/a
26	chr4:715950-716000	HNPCEpiC	eye:	n/a
27	chr4:716657-716707	MCF10A-Er-Src	breast:	n/a
28	chr4:715865-715915	ovcar-3	ovarian:	n/a
29	chr4:716883-716933	GM19239	blood:	n/a
30	chr4:716282-716332	LNCaP	prostate:	n/a
31	chr4:715950-716000	IMR90	lung:	fetal
32	chr4:715872-715922	NH-A	brain:	n/a
33	chr4:715865-715915	HCF	heart:	n/a
34	chr4:715865-715915	IMR90	lung:	fetal
35	chr4:715865-715915	AG10803	skin:	n/a
36	chr4:715865-715915	RPTEC	kidney:	n/a
37	chr4:717040-717090	Hepatocyte	liver:	n/a
38	chr4:716282-716332	AG09309	skin:	n/a
39	chr4:715950-716000	HCF	heart:	n/a
40	chr4:717040-717090	SAEC	small airway:	n/a
41	chr4:717040-717090	NHDF-neo	bronchial:	n/a
42	chr4:715950-716000	H1-hESC	embryonic stem cell:	embryo
43	chr4:717040-717090	PrEC	prostate:	n/a
44	chr4:715950-716000	HL-60	blood:	n/a
45	chr4:716657-716707	PANC-1	pancreas:	n/a
46	chr4:715872-715922	MCF10A-Er-Src	breast:	n/a
47	chr4:715865-715915	MCF10A-Er-Src	breast:	n/a
48	chr4:716282-716332	BJ	skin:	n/a
49	chr4:715950-716000	HPAEpiC	pulmonary alveolar:	n/a
50	chr4:715950-716000	AG09319	gingival:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr4:682540..684982-chr4:715450..717204,2	K562	blood:
2	chr4:673516..676298-chr4:715248..717225,2	K562	blood:
3	chr4:715145..716657-chr4:716815..719761,2	MCF-7	breast:
4	chr4:715797..718296-chr4:723930..726819,3	K562	blood:
5	chr4:707355..710100-chr4:713683..715798,2	MCF-7	breast:
6	chr4:713177..716700-chr4:718880..722359,3	MCF-7	breast:
7	chr4:699453..701203-chr4:715716..717348,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-MFSD7-1	chr4:716064-716226	ENSG00000248416.1
2	lnc-MFSD7-1	chr4:717418-717823	ENSG00000248416.1
3	lnc-MFSD7-1	chr4:716034-716226	NONHSAT094606
4	lnc-MFSD7-1	chr4:717418-717823	NONHSAT094606

No data

Variant related genes	Relation type
PCGF3	TF binding region
ENSG00000248416	TF binding region
PCGF3	CpG island
ENSG00000248416	CpG island
ENSG00000185619	chromatin interactions
ENSG00000215375	chromatin interactions
ENSG00000248416	chromatin interactions
ENSG00000169026	chromatin interactions

Extended variants
information (count: 160 )
Associated
traits (count: 66 )

Variant overlapped rSNPs/rCNVs (count:160 , 50 per page) page: 1 2 3 4

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs189659751	chr4:715801-715802	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
2	rs139685879	chr4:715802-715803	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
3	rs539992378	chr4:715833-715834	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
4	rs558338550	chr4:715842-715843	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
5	rs373811575	chr4:715844-715845	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
6	rs192794522	chr4:715860-715861	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
7	rs576691525	chr4:715872-715873	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
8	rs142590641	chr4:715873-715874	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
9	rs184422321	chr4:715876-715877	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
10	rs529697353	chr4:715918-715919	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
11	rs374081942	chr4:715920-715921	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
12	rs541906698	chr4:715928-715929	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
13	rs373693143	chr4:715958-715959	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers Transcr. at gene 5' and 3' Flanking Active TSS	CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
14	rs150959199	chr4:716005-716006	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers Transcr. at gene 5' and 3' Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
15	rs527394174	chr4:716013-716014	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers Transcr. at gene 5' and 3' Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
16	rs567278896	chr4:716091-716092	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers Transcr. at gene 5' and 3' Active TSS	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
17	rs547183347	chr4:716092-716093	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers Transcr. at gene 5' and 3' Active TSS	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
18	rs188409329	chr4:716102-716103	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers Transcr. at gene 5' and 3' Active TSS	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
19	rs181854759	chr4:716148-716149	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers Transcr. at gene 5' and 3' Active TSS	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
20	rs551328663	chr4:716152-716153	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers Transcr. at gene 5' and 3' Active TSS	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
21	rs569224174	chr4:716162-716163	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers Transcr. at gene 5' and 3' Active TSS	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
22	rs536294381	chr4:716176-716177	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers Transcr. at gene 5' and 3' Active TSS	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
23	rs554951905	chr4:716187-716188	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers Transcr. at gene 5' and 3' Active TSS	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
24	rs149692524	chr4:716198-716199	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers Transcr. at gene 5' and 3' Active TSS	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
25	rs534043049	chr4:716200-716201	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers Transcr. at gene 5' and 3' Active TSS	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
26	rs558301717	chr4:716203-716204	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
27	rs10452329	chr4:716248-716249	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	TF binding region Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
28	rs544091785	chr4:716263-716264	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
29	rs556231883	chr4:716264-716265	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
30	rs368376168	chr4:716272-716273	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
31	rs541421924	chr4:716286-716287	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
32	rs545717888	chr4:716292-716293	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
33	rs560112314	chr4:716299-716300	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
34	rs527355241	chr4:716302-716303	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
35	rs545940132	chr4:716306-716307	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
36	rs148811166	chr4:716314-716315	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
37	rs565459914	chr4:716315-716316	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
38	rs532792814	chr4:716325-716326	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
39	rs111979588	chr4:716327-716328	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	mRNA abundance
40	rs562993517	chr4:716379-716380	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
41	rs184794562	chr4:716380-716381	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
42	rs530430331	chr4:716381-716382	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
43	rs548254501	chr4:716387-716388	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
44	rs113162348	chr4:716392-716393	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
45	rs377210969	chr4:716399-716400	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
46	rs112681541	chr4:716400-716401	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
47	rs35232439	chr4:716421-716422	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
48	rs566880222	chr4:716428-716429	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
49	rs113600723	chr4:716454-716455	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
50	rs75901702	chr4:716463-716464	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:66)

Disease	PMID	Source
Myelofibrosis	22110671	CNVD
Wolf-Hirschhorn syndrome	21549014	CNVD
Breast cancer	21806811	CNVD
Wolf-Hirschhorn syndrome	22283845	CNVD
Wolf-Hirschhorn syndrome	16773131	CNVD
Mental retardation	16773131	CNVD
Wolf-Hirschhorn syndrome	22470819	CNVD
Wolf-Hirschhorn syndrome	18541967	CNVD
sporadic birth defects	19047251	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Retinitis pigmentosa	18421352	CNVD
Wolf-Hirschhorn syndrome	19259404	CNVD
Bladder cancer	19242612	CNVD
Breast cancer	19242612	CNVD
Congenital anomalies of the kidney and urinary tract	19242612	CNVD
abnormal development	18461090	CNVD
Olfactory neuroblastoma	18408657	CNVD
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
Breast cancer	17142309	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Developmental delay	21147756	CNVD
Urothelial carcinoma	21177765	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Lung cancer	18438408	CNVD
Prostate cancer	18632612	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Breast cancer	21509527	CNVD
Pancreatic cancer	17952125	CNVD
Type 2 diabetes	21754918	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:292 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:701200-724400	Weak transcription	Aorta	Aorta
2	chr4:701400-724400	Weak transcription	HUES64 Cell Line	embryonic stem cell
3	chr4:701400-724800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
4	chr4:701600-716800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
5	chr4:702200-754800	Weak transcription	Hela-S3	cervix
6	chr4:702400-720000	Weak transcription	Brain Substantia Nigra	brain
7	chr4:702400-720200	Weak transcription	NH-A	brain
8	chr4:702600-715800	Weak transcription	Liver	Liver
9	chr4:702600-716800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
10	chr4:702600-724400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
11	chr4:702800-726600	Weak transcription	Primary B cells from cord blood	blood
12	chr4:703000-716600	Weak transcription	Fetal Lung	lung
13	chr4:703400-717800	Weak transcription	Rectal Smooth Muscle	rectum
14	chr4:703400-724800	Weak transcription	Primary T helper cells fromperipheralblood	blood
15	chr4:703400-726800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
16	chr4:703600-727200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
17	chr4:703800-724400	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
18	chr4:704000-724400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
19	chr4:704200-715800	Weak transcription	H1 Cell Line	embryonic stem cell
20	chr4:704400-721200	Weak transcription	Small Intestine	intestine
21	chr4:704400-721400	Weak transcription	A549	lung
22	chr4:704600-727600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
23	chr4:704800-724600	Weak transcription	HUES48 Cell Line	embryonic stem cell
24	chr4:705000-724400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
25	chr4:708200-736400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
26	chr4:708600-716000	Weak transcription	Fetal Thymus	thymus
27	chr4:708600-716600	Weak transcription	Duodenum Smooth Muscle	Duodenum
28	chr4:708600-719400	Weak transcription	Osteobl	bone
29	chr4:708800-715800	Weak transcription	HUES6 Cell Line	embryonic stem cell
30	chr4:708800-717800	Weak transcription	Rectal Mucosa Donor 29	rectum
31	chr4:709200-715800	Weak transcription	Stomach Smooth Muscle	stomach
32	chr4:709200-724400	Weak transcription	Primary T cells fromperipheralblood	blood
33	chr4:709200-726200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
34	chr4:709200-726200	Weak transcription	Primary T helper cells PMA-I stimulated	--
35	chr4:710600-717400	Strong transcription	Fetal Intestine Small	intestine
36	chr4:711200-718400	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
37	chr4:711200-718800	ZNF genes & repeats	Fetal Stomach	stomach
38	chr4:711400-716000	Enhancers	Fetal Muscle Leg	muscle
39	chr4:711800-724400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
40	chr4:713000-715800	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
41	chr4:713000-718200	ZNF genes & repeats	Brain Germinal Matrix	brain
42	chr4:713200-717200	Genic enhancers	Spleen	Spleen
43	chr4:713200-718000	Strong transcription	Dnd41	blood
44	chr4:713200-719400	ZNF genes & repeats	H9 Derived Neuron Cultured Cells	ES cell derived
45	chr4:713400-716200	Enhancers	Right Ventricle	heart
46	chr4:713400-717400	Genic enhancers	Fetal Muscle Trunk	muscle
47	chr4:713400-717600	Strong transcription	H9 Cell Line	embryonic stem cell
48	chr4:713400-718600	Strong transcription	Primary hematopoietic stem cells short term culture	blood
49	chr4:713400-727600	Weak transcription	Pancreatic Islets	Pancreatic Islet
50	chr4:713600-716000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--

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