Variant report

Variant	esv3422247
Chromosome Location	chr4:166247552-166250050
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:567)
CpG islands
(count:1039)
Chromatin interactive
region (count:7)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:567 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:166248161-166249019	K562	blood:	n/a	n/a
2	ARID3A	chr4:166247191-166247569	HepG2	liver:	n/a	n/a
3	ARID3A	chr4:166248780-166249032	HepG2	liver:	n/a	n/a
4	ARID3A	chr4:166248159-166248461	HepG2	liver:	n/a	n/a
5	ARID3A	chr4:166247006-166247696	K562	blood:	n/a	n/a
6	ARID3A	chr4:166249958-166250246	HepG2	liver:	n/a	n/a
7	ATF1	chr4:166248249-166248915	K562	blood:	n/a	n/a
8	ATF2	chr4:166247997-166248824	GM12878	blood:	n/a	n/a
9	ATF2	chr4:166248110-166248579	H1-hESC	embryonic stem cell:	n/a	n/a
10	ATF3	chr4:166248957-166249286	A549	lung:	n/a	n/a
11	BACH1	chr4:166246628-166247753	K562	blood:	n/a	n/a
12	BACH1	chr4:166246888-166249025	H1-hESC	embryonic stem cell:	n/a	n/a
13	BCLAF1	chr4:166248701-166249299	GM12878	blood:	n/a	n/a
14	BHLHE40	chr4:166248423-166249216	HepG2	liver:	n/a	chr4:166248691-166248707
15	BHLHE40	chr4:166248084-166249474	K562	blood:	n/a	chr4:166248691-166248707
16	BHLHE40	chr4:166248159-166249202	GM12878	blood:	n/a	chr4:166248691-166248707
17	BRCA1	chr4:166248437-166249213	HepG2	liver:	n/a	n/a
18	BRCA1	chr4:166248271-166249058	Hela-S3	cervix:	n/a	n/a
19	BRCA1	chr4:166248648-166249063	H1-hESC	embryonic stem cell:	n/a	n/a
20	CBX3	chr4:166246619-166247821	HCT-116	colon:	n/a	n/a
21	CBX3	chr4:166248212-166249213	K562	blood:	n/a	n/a
22	CBX3	chr4:166246426-166247773	HCT-116	colon:	n/a	n/a
23	CCNT2	chr4:166248147-166249431	K562	blood:	n/a	n/a
24	CEBPB	chr4:166247959-166248843	HepG2	liver:	n/a	n/a
25	CEBPB	chr4:166248925-166249018	H1-hESC	embryonic stem cell:	n/a	n/a
26	CEBPB	chr4:166247931-166248886	Hela-S3	cervix:	n/a	n/a
27	CEBPB	chr4:166248007-166249501	IMR90	lung:	n/a	n/a
28	CEBPB	chr4:166247951-166248303	MCF-7	breast:	n/a	n/a
29	CEBPB	chr4:166246917-166247683	K562	blood:	n/a	n/a
30	CEBPB	chr4:166246905-166247594	IMR90	lung:	n/a	n/a
31	CEBPB	chr4:166247921-166249109	HepG2	liver:	n/a	n/a
32	CEBPB	chr4:166247965-166248769	K562	blood:	n/a	n/a
33	CEBPB	chr4:166247983-166248553	K562	blood:	n/a	n/a
34	CEBPB	chr4:166247944-166248764	A549	lung:	n/a	n/a
35	CEBPB	chr4:166248030-166248214	HepG2	liver:	n/a	n/a
36	CEBPD	chr4:166248708-166249106	HepG2	liver:	n/a	n/a
37	CEBPZ	chr4:166248576-166248844	HepG2	liver:	n/a	n/a
38	CHD1	chr4:166249526-166249624	H1-hESC	embryonic stem cell:	n/a	n/a
39	CHD1	chr4:166248878-166249279	H1-hESC	embryonic stem cell:	n/a	n/a
40	CHD1	chr4:166247763-166249723	GM12878	blood:	n/a	n/a
41	CHD2	chr4:166248091-166249418	GM12878	blood:	n/a	n/a
42	CHD2	chr4:166248116-166249243	Hela-S3	cervix:	n/a	n/a
43	CHD2	chr4:166248155-166249216	H1-hESC	embryonic stem cell:	n/a	n/a
44	CHD2	chr4:166248227-166249383	K562	blood:	n/a	n/a
45	CHD2	chr4:166248239-166249439	HepG2	liver:	n/a	n/a
46	CREB1	chr4:166248347-166249240	A549	lung:	n/a	n/a
47	CREB1	chr4:166248300-166249225	HepG2	liver:	n/a	n/a
48	CREB1	chr4:166247971-166249261	K562	blood:	n/a	n/a
49	CREB1	chr4:166248523-166248905	A549	lung:	n/a	n/a
50	CREB1	chr4:166248412-166249050	ECC-1	luminal epithelium:	n/a	n/a

(count:1039 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:166248715-166248765	AG04450	lung:	fetal
2	chr4:166248057-166248107	HMEC	breast:	n/a
3	chr4:166248715-166248765	AG04450	lung:	fetal
4	chr4:166248057-166248107	HMEC	breast:	n/a
5	chr4:166248625-166248675	AG04449	skin:	fetal
6	chr4:166248625-166248675	CMK	blood:	n/a
7	chr4:166248820-166248870	HL-60	blood:	n/a
8	chr4:166248467-166248517	BE2_C	brain:	n/a
9	chr4:166248625-166248675	HEK293	kidney:	embryo
10	chr4:166248625-166248675	AG10803	skin:	n/a
11	chr4:166248399-166248449	AoSMC	blood vessel:	n/a
12	chr4:166248713-166248763	Hepatocyte	liver:	n/a
13	chr4:166248625-166248675	HCPEpiC	choroid plexus:	n/a
14	chr4:166248124-166248174	GM12878	blood:	n/a
15	chr4:166248713-166248763	U87	brain:	n/a
16	chr4:166248715-166248765	BJ	skin:	n/a
17	chr4:166248219-166248269	HIPEpiC	eye:	n/a
18	chr4:166248713-166248763	AG09319	gingival:	n/a
19	chr4:166248219-166248269	NB4	blood:	n/a
20	chr4:166248713-166248763	ECC-1	luminal epithelium:	n/a
21	chr4:166248675-166248725	H1-hESC	embryonic stem cell:	embryo
22	chr4:166248219-166248269	GM06990	blood:	n/a
23	chr4:166248219-166248269	SK-N-SH	brain:	n/a
24	chr4:166248124-166248174	CMK	blood:	n/a
25	chr4:166248713-166248763	PANC-1	pancreas:	n/a
26	chr4:166248675-166248725	HNPCEpiC	eye:	n/a
27	chr4:166248618-166248668	HepG2	liver:	n/a
28	chr4:166248675-166248725	NH-A	brain:	n/a
29	chr4:166248820-166248870	BJ	skin:	n/a
30	chr4:166248618-166248668	SK-N-MC	brain:	n/a
31	chr4:166249239-166249289	GM06990	blood:	n/a
32	chr4:166248715-166248765	GM06990	blood:	n/a
33	chr4:166249014-166249064	BE2_C	brain:	n/a
34	chr4:166248675-166248725	ProgFib	skin:	n/a
35	chr4:166248219-166248269	SKMC	muscle:	n/a
36	chr4:166248675-166248725	MCF-7	breast:	n/a
37	chr4:166249203-166249253	K562	blood:	n/a
38	chr4:166248467-166248517	Hepatocyte	liver:	n/a
39	chr4:166248713-166248763	K562	blood:	n/a
40	chr4:166248399-166248449	HAEpiC	amniotic membrane:	n/a
41	chr4:166248625-166248675	AG09319	gingival:	n/a
42	chr4:166248715-166248765	NHBE	bronchial:	n/a
43	chr4:166249203-166249253	GM12892	blood:	n/a
44	chr4:166248807-166248857	Hela-S3	cervix:	n/a
45	chr4:166248713-166248763	HMEC	breast:	n/a
46	chr4:166249239-166249289	SK-N-SH	brain:	n/a
47	chr4:166248057-166248107	BJ	skin:	n/a
48	chr4:166249203-166249253	GM12891	blood:	n/a
49	chr4:166248675-166248725	HIPEpiC	eye:	n/a
50	chr4:166248124-166248174	SK-N-MC	brain:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr4:166127276..166130366-chr4:166247405..166250443,3	K562	blood:
2	chr4:166127386..166130072-chr4:166247171..166250406,6	MCF-7	breast:
3	chr4:166249129..166252121-chr4:166265324..166266921,2	K562	blood:
4	chr4:166033415..166035712-chr4:166248207..166249791,2	MCF-7	breast:
5	chr4:166033254..166035775-chr4:166247057..166248909,2	MCF-7	breast:
6	chr4:166128531..166130929-chr4:166246215..166249595,5	MCF-7	breast:
7	chr4:166126308..166130366-chr4:166247405..166251145,5	K562	blood:

No data

Variant related genes	Relation type
MSMO1	TF binding region
MSMO1	CpG island
ENSG00000109466	chromatin interactions
ENSG00000170088	chromatin interactions

Extended variants
information (count: 110 )
Associated
traits (count: 74 )

Variant overlapped rSNPs/rCNVs (count:110 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs544429556	chr4:166247571-166247572	Flanking Active TSS Enhancers Weak transcription Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
2	rs551295279	chr4:166247583-166247584	Flanking Active TSS Enhancers Weak transcription Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs144034830	chr4:166247584-166247585	Flanking Active TSS Enhancers Weak transcription Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs181628678	chr4:166247649-166247650	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs184279682	chr4:166247650-166247651	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs560479938	chr4:166247654-166247655	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs145368061	chr4:166247661-166247662	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs527725404	chr4:166247712-166247713	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs375078648	chr4:166247722-166247723	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs567985458	chr4:166247729-166247730	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs374600324	chr4:166247797-166247798	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs531799737	chr4:166247811-166247812	Active TSS Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs550316994	chr4:166247818-166247819	Active TSS Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs369071765	chr4:166247866-166247867	Active TSS Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs571771333	chr4:166247871-166247872	Active TSS Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs539474063	chr4:166247909-166247910	Active TSS Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs557441382	chr4:166247932-166247933	Active TSS Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs566122563	chr4:166247978-166247979	Active TSS Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs533590215	chr4:166248023-166248024	Active TSS Flanking Active TSS ZNF genes & repeats Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs35597788	chr4:166248035-166248036	Active TSS Flanking Active TSS ZNF genes & repeats Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs550552519	chr4:166248040-166248041	Active TSS Flanking Active TSS ZNF genes & repeats Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs57337930	chr4:166248041-166248042	Active TSS Flanking Active TSS ZNF genes & repeats Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs200285409	chr4:166248054-166248055	Active TSS Flanking Active TSS ZNF genes & repeats Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs372281580	chr4:166248080-166248081	Active TSS Flanking Active TSS ZNF genes & repeats Weak transcription	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs555220814	chr4:166248089-166248090	Active TSS Flanking Active TSS ZNF genes & repeats Weak transcription	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs115131331	chr4:166248100-166248101	Active TSS Flanking Active TSS ZNF genes & repeats Weak transcription	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs544200139	chr4:166248116-166248117	Active TSS Flanking Active TSS ZNF genes & repeats Weak transcription	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs368045793	chr4:166248120-166248121	Active TSS Flanking Active TSS ZNF genes & repeats Weak transcription	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs556276060	chr4:166248188-166248189	Active TSS Flanking Active TSS ZNF genes & repeats Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs10009994	chr4:166248202-166248203	Active TSS Flanking Active TSS ZNF genes & repeats Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
31	rs149197858	chr4:166248206-166248207	Active TSS Flanking Active TSS ZNF genes & repeats Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs560612980	chr4:166248213-166248214	Active TSS Flanking Active TSS ZNF genes & repeats Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs527662047	chr4:166248241-166248242	Active TSS Flanking Active TSS ZNF genes & repeats Weak transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs188702281	chr4:166248297-166248298	Active TSS Flanking Active TSS ZNF genes & repeats Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs557023356	chr4:166248445-166248446	Active TSS ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs561285363	chr4:166248468-166248469	Active TSS ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs532005800	chr4:166248481-166248482	Active TSS ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs550212490	chr4:166248487-166248488	Active TSS ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs75102336	chr4:166248499-166248500	Active TSS ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs373856204	chr4:166248508-166248509	Active TSS ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs369091120	chr4:166248520-166248521	Active TSS ZNF genes & repeats Bivalent/Poised TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs571772884	chr4:166248550-166248551	Active TSS ZNF genes & repeats Bivalent/Poised TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs3836623	chr4:166248552-166248553	Active TSS ZNF genes & repeats Bivalent/Poised TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs397841172	chr4:166248555-166248556	Active TSS ZNF genes & repeats Bivalent/Poised TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs200045172	chr4:166248556-166248557	Active TSS ZNF genes & repeats Bivalent/Poised TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs367695562	chr4:166248579-166248580	Active TSS ZNF genes & repeats Bivalent/Poised TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs532637317	chr4:166248583-166248584	Active TSS ZNF genes & repeats Bivalent/Poised TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs551059585	chr4:166248618-166248619	Active TSS ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs34072687	chr4:166248621-166248622	Active TSS ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs9998426	chr4:166248623-166248624	Active TSS ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:74)

Disease	PMID	Source
Acute lymphoblastic leukemia	22237106	CNVD
Glioblastoma multiforme	21080181	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Chordoma	21602918	CNVD
HIV/AIDS	22032296	CNVD
Medulloblastoma	21979893	CNVD
Neuroblastoma	18923191	CNVD
Breast cancer	21858162	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Gastric cancer	21586687	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17603634	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Colorectal cancer	19359472	CNVD
Malignant mesothelioma	18160781	CNVD
Medulloblastoma	18056178	CNVD
Multiple myeloma	17077331	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Oral squamous cell carcinoma	17134496	CNVD
4q-syndrome	17576883	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Colorectal cancer	20709793	CNVD
Muscular dystrophy	21149563	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Cervical cancer	21062161	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	16608533	CNVD
Lung cancer	19208797	CNVD
Wilms tumour	21544195	CNVD
Lung cancer	18438408	CNVD
Cancer	22429812	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
primary effusion lymphomas	17116491	CNVD
Breast cancer	16272173	CNVD
Breast cancer	17133270	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Congenital anomalies of the kidney and urinary tract	20505237	CNVD
Breast cancer	17393978	CNVD
Testicular germ cell tumor	18059402	CNVD
Ovarian cancer	22174824	CNVD
Olfactory neuroblastoma	18408657	CNVD
Breast cancer	21785460	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Hodgkin''s lymphoma	17606441	CNVD
small cell lung cancer	20016488	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Ewing''s sarcoma	17952124	CNVD
Breast cancer	21633010	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Cancer	20581869	CNVD
Glioblastoma multiforme	22286061	CNVD
Basal cell lymphoma	17053054	CNVD
Hepatocellular carcinoma	16750200	CNVD
Colorectal cancer	16774939	CNVD
Esophageal squamous carcinoma	17470683	CNVD
Myelofibrosis	22110671	CNVD
intellectual deficit	22127048	CNVD
abnormal development	18461090	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:429 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:166220000-166247800	Weak transcription	Right Ventricle	heart
2	chr4:166223400-166247600	Weak transcription	Thymus	Thymus
3	chr4:166223400-166247800	Weak transcription	Aorta	Aorta
4	chr4:166223400-166248000	Weak transcription	Gastric	stomach
5	chr4:166223600-166247600	Weak transcription	Fetal Lung	lung
6	chr4:166223800-166247600	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
7	chr4:166224200-166247600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
8	chr4:166224400-166247600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
9	chr4:166233000-166248000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
10	chr4:166233400-166247600	Weak transcription	Adipose Nuclei	Adipose
11	chr4:166233400-166247800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
12	chr4:166233400-166248000	Weak transcription	Left Ventricle	heart
13	chr4:166234000-166247600	Weak transcription	Rectal Mucosa Donor 29	rectum
14	chr4:166241000-166247800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
15	chr4:166241800-166247600	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
16	chr4:166245400-166247600	Enhancers	HMEC	breast
17	chr4:166245800-166247600	Enhancers	Fetal Intestine Large	intestine
18	chr4:166246400-166247600	Enhancers	iPS-15b Cell Line	embryonic stem cell
19	chr4:166246600-166247600	Enhancers	Primary neutrophils fromperipheralblood	blood
20	chr4:166246600-166247600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
21	chr4:166246600-166247600	Enhancers	Psoas Muscle	Psoas
22	chr4:166246600-166247800	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
23	chr4:166246600-166247800	Enhancers	Esophagus	oesophagus
24	chr4:166246600-166248000	Enhancers	Placenta	Placenta
25	chr4:166246600-166248000	Enhancers	Pancreas	Pancrea
26	chr4:166246800-166247600	Enhancers	Primary T cells fromperipheralblood	blood
27	chr4:166246800-166247800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
28	chr4:166246800-166247800	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
29	chr4:166246800-166247800	Enhancers	Primary monocytes fromperipheralblood	blood
30	chr4:166246800-166247800	Enhancers	Ovary	ovary
31	chr4:166246800-166247800	Flanking Active TSS	K562	blood
32	chr4:166246800-166248000	Enhancers	Placenta Amnion	Placenta Amnion
33	chr4:166246800-166248000	Enhancers	Sigmoid Colon	Sigmoid Colon
34	chr4:166246800-166248200	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
35	chr4:166247000-166247600	Enhancers	Primary B cells from cord blood	blood
36	chr4:166247000-166247600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
37	chr4:166247000-166247600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
38	chr4:166247000-166247800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
39	chr4:166247000-166247800	Enhancers	Spleen	Spleen
40	chr4:166247000-166247800	Flanking Active TSS	HepG2	liver
41	chr4:166247000-166248000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
42	chr4:166247000-166248000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
43	chr4:166247000-166248000	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
44	chr4:166247000-166248000	Flanking Active TSS	Muscle Satellite Cultured Cells	--
45	chr4:166247000-166248000	Flanking Active TSS	Hela-S3	cervix
46	chr4:166247000-166248000	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
47	chr4:166247000-166251600	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
48	chr4:166247200-166247600	Flanking Active TSS	ES-I3 Cell Line	embryonic stem cell
49	chr4:166247200-166247600	Enhancers	Cortex derived primary cultured neurospheres	brain
50	chr4:166247200-166247600	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin

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