Variant report

Variant	esv3421353
Chromosome Location	chr4:723402-725900
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:56)
CpG islands
(count:183)
Chromatin interactive
region (count:7)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:56 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CBX3	chr4:725085-726034	K562	blood:	n/a	n/a
2	CCNT2	chr4:724844-724857	K562	blood:	n/a	n/a
3	CCNT2	chr4:725207-725407	K562	blood:	n/a	n/a
4	CEBPD	chr4:725545-726059	K562	blood:	n/a	n/a
5	CHD2	chr4:725067-725083	K562	blood:	n/a	n/a
6	EGR1	chr4:725155-725505	K562	blood:	n/a	n/a
7	EGR1	chr4:725738-726092	K562	blood:	n/a	n/a
8	EGR1	chr4:725751-726098	K562	blood:	n/a	n/a
9	EGR1	chr4:725181-725413	K562	blood:	n/a	n/a
10	ELF1	chr4:724272-724583	GM12878	blood:	n/a	chr4:724375-724384
11	ELF1	chr4:723585-723975	GM12878	blood:	n/a	n/a
12	GABPA	chr4:725499-725737	Hela-S3	cervix:	n/a	n/a
13	GABPA	chr4:725263-726093	Hela-S3	cervix:	n/a	n/a
14	HDAC2	chr4:725160-725371	K562	blood:	n/a	n/a
15	HDAC2	chr4:725732-725900	K562	blood:	n/a	n/a
16	HMGN3	chr4:724858-725278	K562	blood:	n/a	n/a
17	IRF1	chr4:725773-726147	K562	blood:	n/a	n/a
18	IRF1	chr4:725114-725548	K562	blood:	n/a	n/a
19	MAX	chr4:725162-725424	K562	blood:	n/a	n/a
20	MAX	chr4:725274-725469	K562	blood:	n/a	n/a
21	MAX	chr4:725731-726057	K562	blood:	n/a	n/a
22	MAX	chr4:725068-725514	K562	blood:	n/a	n/a
23	MAX	chr4:725749-725955	K562	blood:	n/a	n/a
24	MAX	chr4:725794-726096	K562	blood:	n/a	n/a
25	MAZ	chr4:725187-725471	K562	blood:	n/a	n/a
26	MAZ	chr4:725786-726187	K562	blood:	n/a	n/a
27	MYC	chr4:725829-726010	K562	blood:	n/a	n/a
28	NR2F2	chr4:725489-725840	K562	blood:	n/a	n/a
29	POLR2A	chr4:725475-726009	GM12892	blood:	n/a	n/a
30	POLR2A	chr4:725451-725943	GM12891	blood:	n/a	n/a
31	POLR2A	chr4:723599-724119	SK-N-MC	brain:	n/a	n/a
32	POLR2A	chr4:724802-725002	K562	blood:	n/a	n/a
33	POLR2A	chr4:725461-725834	H1-hESC	embryonic stem cell:	n/a	n/a
34	POLR2A	chr4:723823-723986	GM12878	blood:	n/a	n/a
35	POLR2A	chr4:724370-724387	K562	blood:	n/a	n/a
36	POLR2A	chr4:724522-724540	ProgFib	skin:	n/a	n/a
37	POLR2A	chr4:725472-725976	GM12878	blood:	n/a	n/a
38	POLR2A	chr4:723616-724010	K562	blood:	n/a	n/a
39	POLR2A	chr4:724279-724309	K562	blood:	n/a	n/a
40	POLR2A	chr4:724567-724646	ProgFib	skin:	n/a	n/a
41	POLR2A	chr4:724407-724416	K562	blood:	n/a	n/a
42	POLR2A	chr4:724180-724210	HUVEC	blood vessel:	n/a	n/a
43	POLR2A	chr4:725356-726008	GM12878	blood:	n/a	n/a
44	REST	chr4:725440-725677	PANC-1	pancreas:	n/a	n/a
45	SIN3AK20	chr4:725740-726029	K562	blood:	n/a	n/a
46	SIN3AK20	chr4:725230-725437	K562	blood:	n/a	n/a
47	SP1	chr4:725368-725962	A549	lung:	n/a	n/a
48	SP1	chr4:725165-726080	K562	blood:	n/a	n/a
49	SP1	chr4:725379-725784	GM12878	blood:	n/a	n/a
50	TCF3	chr4:725445-725919	GM12878	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	chr4:725095-725145	HUVEC	blood vessel:	n/a
2	chr4:725336-725386	BJ	skin:	n/a
3	chr4:725095-725145	GM19239	blood:	n/a
4	chr4:725336-725386	HRE	kidney:	n/a
5	chr4:725095-725145	U87	brain:	n/a
6	chr4:725095-725145	IMR90	lung:	fetal
7	chr4:725336-725386	AG10803	skin:	n/a
8	chr4:725336-725386	NHBE	bronchial:	n/a
9	chr4:725336-725386	T-47D	breast:	n/a
10	chr4:724723-724773	ovcar-3	ovarian:	n/a
11	chr4:724723-724773	NT2-D1	testis:	n/a
12	chr4:725095-725145	NH-A	brain:	n/a
13	chr4:724723-724773	BJ	skin:	n/a
14	chr4:724723-724773	SK-N-MC	brain:	n/a
15	chr4:724723-724773	LNCaP	prostate:	n/a
16	chr4:725095-725145	MCF10A-Er-Src	breast:	n/a
17	chr4:725336-725386	AoSMC	blood vessel:	n/a
18	chr4:725336-725386	HPAEpiC	pulmonary alveolar:	n/a
19	chr4:724723-724773	MCF10A-Er-Src	breast:	n/a
20	chr4:725336-725386	NB4	blood:	n/a
21	chr4:724723-724773	GM06990	blood:	n/a
22	chr4:725095-725145	NHBE	bronchial:	n/a
23	chr4:725336-725386	ProgFib	skin:	n/a
24	chr4:724723-724773	NH-A	brain:	n/a
25	chr4:725095-725145	AG09309	skin:	n/a
26	chr4:725336-725386	PFSK-1	brain:	n/a
27	chr4:725336-725386	BE2_C	brain:	n/a
28	chr4:725336-725386	HRPEpiC	eye:	n/a
29	chr4:724723-724773	AG10803	skin:	n/a
30	chr4:725095-725145	AoSMC	blood vessel:	n/a
31	chr4:725095-725145	HRCEpiC	kidney:	n/a
32	chr4:724723-724773	BE2_C	brain:	n/a
33	chr4:725336-725386	NH-A	brain:	n/a
34	chr4:725336-725386	HRCEpiC	kidney:	n/a
35	chr4:725095-725145	NT2-D1	testis:	n/a
36	chr4:725095-725145	CMK	blood:	n/a
37	chr4:725095-725145	HCPEpiC	choroid plexus:	n/a
38	chr4:725095-725145	NB4	blood:	n/a
39	chr4:724723-724773	HRE	kidney:	n/a
40	chr4:725336-725386	SK-N-SH	brain:	n/a
41	chr4:725336-725386	ECC-1	luminal epithelium:	n/a
42	chr4:725095-725145	AG04449	skin:	fetal
43	chr4:725336-725386	HEK293	kidney:	embryo
44	chr4:724723-724773	HCT-116	colon:	n/a
45	chr4:725336-725386	K562	blood:	n/a
46	chr4:725336-725386	IMR90	lung:	fetal
47	chr4:725095-725145	SKMC	muscle:	n/a
48	chr4:725095-725145	SK-N-SH	brain:	n/a
49	chr4:725095-725145	HL-60	blood:	n/a
50	chr4:725095-725145	HMEC	breast:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr4:701224..703407-chr4:720806..724106,3	K562	blood:
2	chr4:725258..728014-chr4:756169..758632,2	MCF-7	breast:
3	chr4:718839..721866-chr4:723337..725230,5	K562	blood:
4	chr4:718846..721970-chr4:722068..726476,6	K562	blood:
5	chr4:676118..678375-chr4:722491..724316,2	K562	blood:
6	chr4:723040..724822-chr4:760521..763494,2	K562	blood:
7	chr4:715797..718296-chr4:723930..726819,3	K562	blood:

No data

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

Extended variants
information (count: 147 )
Associated
traits (count: 66 )

Variant overlapped rSNPs/rCNVs (count:147 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs114047292	chr4:723468-723469	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs535609964	chr4:723552-723553	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs149712460	chr4:723575-723576	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs572374587	chr4:723578-723579	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs116194160	chr4:723662-723663	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs78838194	chr4:723665-723666	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs146214559	chr4:723672-723673	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs543896630	chr4:723703-723704	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs562119831	chr4:723718-723719	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs574191418	chr4:723719-723720	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs541194450	chr4:723728-723729	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs564879416	chr4:723744-723745	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs370929915	chr4:723776-723777	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs532219965	chr4:723781-723782	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs12513163	chr4:723785-723786	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs139155358	chr4:723805-723806	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs551427025	chr4:723857-723858	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs4317149	chr4:723882-723883	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
19	rs144037789	chr4:723884-723885	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs146438620	chr4:723912-723913	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs566986102	chr4:723928-723929	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs528193370	chr4:723931-723932	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs185668153	chr4:723940-723941	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs566174101	chr4:723973-723974	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs368645698	chr4:723998-723999	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs190730596	chr4:724029-724030	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs570333233	chr4:724030-724031	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs11735280	chr4:724061-724062	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
29	rs555815950	chr4:724063-724064	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs574154439	chr4:724067-724068	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs373580118	chr4:724069-724070	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs372587652	chr4:724097-724098	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs541567358	chr4:724121-724122	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs12500281	chr4:724167-724168	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs553193923	chr4:724168-724169	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs577807195	chr4:724202-724203	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs545190776	chr4:724224-724225	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs563395264	chr4:724236-724237	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs530847730	chr4:724255-724256	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs191949839	chr4:724259-724260	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs560575207	chr4:724263-724264	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs11932342	chr4:724323-724324	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs546332904	chr4:724353-724354	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs367720175	chr4:724388-724389	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs533320274	chr4:724446-724447	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs551963134	chr4:724449-724450	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs570220233	chr4:724464-724465	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs142464906	chr4:724475-724476	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs371546177	chr4:724476-724477	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs375390826	chr4:724493-724494	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	3 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:272 , 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	chr4:702200-754800	Weak transcription	Hela-S3	cervix
5	chr4:702600-724400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
6	chr4:702800-726600	Weak transcription	Primary B cells from cord blood	blood
7	chr4:703400-724800	Weak transcription	Primary T helper cells fromperipheralblood	blood
8	chr4:703400-726800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
9	chr4:703600-727200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
10	chr4:703800-724400	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
11	chr4:704000-724400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
12	chr4:704600-727600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
13	chr4:704800-724600	Weak transcription	HUES48 Cell Line	embryonic stem cell
14	chr4:705000-724400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
15	chr4:708200-736400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
16	chr4:709200-724400	Weak transcription	Primary T cells fromperipheralblood	blood
17	chr4:709200-726200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
18	chr4:709200-726200	Weak transcription	Primary T helper cells PMA-I stimulated	--
19	chr4:711800-724400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
20	chr4:713400-727600	Weak transcription	Pancreatic Islets	Pancreatic Islet
21	chr4:714200-726200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
22	chr4:715200-724400	Weak transcription	Primary B cells from peripheral blood	blood
23	chr4:715200-726200	Weak transcription	HMEC	breast
24	chr4:715600-750200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
25	chr4:716200-724400	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
26	chr4:716400-724600	Weak transcription	NHEK	skin
27	chr4:716800-724800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
28	chr4:717000-724200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
29	chr4:717000-724400	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
30	chr4:717200-724200	Weak transcription	Primary T cells from cord blood	blood
31	chr4:717200-724400	Weak transcription	GM12878-XiMat	blood
32	chr4:717600-724400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
33	chr4:717600-724400	Weak transcription	H9 Cell Line	embryonic stem cell
34	chr4:717800-723600	Weak transcription	Placenta Amnion	Placenta Amnion
35	chr4:717800-723800	Weak transcription	Primary monocytes fromperipheralblood	blood
36	chr4:717800-723800	Weak transcription	Primary neutrophils fromperipheralblood	blood
37	chr4:717800-724400	Weak transcription	H1 Cell Line	embryonic stem cell
38	chr4:717800-724400	Weak transcription	Duodenum Smooth Muscle	Duodenum
39	chr4:718000-724600	Weak transcription	Fetal Lung	lung
40	chr4:718200-723800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
41	chr4:718200-723800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
42	chr4:718200-724600	Weak transcription	Rectal Smooth Muscle	rectum
43	chr4:718400-735400	Weak transcription	Fetal Heart	heart
44	chr4:718600-732600	Weak transcription	Stomach Mucosa	stomach
45	chr4:718800-724600	Weak transcription	HepG2	liver
46	chr4:719000-733000	Strong transcription	Fetal Intestine Small	intestine
47	chr4:719400-724400	Weak transcription	Rectal Mucosa Donor 29	rectum
48	chr4:719800-724600	Weak transcription	Colonic Mucosa	Colon
49	chr4:720000-724400	Weak transcription	Rectal Mucosa Donor 31	rectum
50	chr4:720000-738400	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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