Variant report

Variant	nsv967728
Chromosome Location	chr4:16229943-16232845
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:16230039-16230251	K562	blood:	n/a	n/a
2	CEBPB	chr4:16231245-16231592	HepG2	liver:	n/a	chr4:16231420-16231431 chr4:16231420-16231433 chr4:16231422-16231431 chr4:16231422-16231431 chr4:16231422-16231431 chr4:16231356-16231367 chr4:16231354-16231367
3	CEBPB	chr4:16231254-16231592	A549	lung:	n/a	chr4:16231420-16231431 chr4:16231420-16231433 chr4:16231422-16231431 chr4:16231422-16231431 chr4:16231422-16231431 chr4:16231356-16231367 chr4:16231354-16231367
4	CEBPB	chr4:16231287-16231559	H1-hESC	embryonic stem cell:	n/a	chr4:16231420-16231431 chr4:16231420-16231433 chr4:16231422-16231431 chr4:16231422-16231431 chr4:16231422-16231431 chr4:16231356-16231367 chr4:16231354-16231367
5	CEBPB	chr4:16231225-16231606	K562	blood:	n/a	chr4:16231420-16231431 chr4:16231420-16231433 chr4:16231422-16231431 chr4:16231422-16231431 chr4:16231422-16231431 chr4:16231356-16231367 chr4:16231354-16231367
6	CEBPB	chr4:16231302-16231579	Hela-S3	cervix:	n/a	chr4:16231420-16231431 chr4:16231420-16231433 chr4:16231422-16231431 chr4:16231422-16231431 chr4:16231422-16231431 chr4:16231356-16231367 chr4:16231354-16231367
7	CEBPB	chr4:16231235-16231605	IMR90	lung:	n/a	chr4:16231420-16231431 chr4:16231420-16231433 chr4:16231422-16231431 chr4:16231422-16231431 chr4:16231422-16231431 chr4:16231356-16231367 chr4:16231354-16231367
8	E2F4	chr4:16231216-16231419	MCF10A-Er-Src	breast:	n/a	n/a
9	EP300	chr4:16230359-16230545	K562	blood:	n/a	n/a
10	EP300	chr4:16232745-16232788	K562	blood:	n/a	n/a
11	HEY1	chr4:16229732-16230063	K562	blood:	n/a	n/a
12	IRF1	chr4:16230236-16230642	K562	blood:	n/a	chr4:16230440-16230457
13	IRF1	chr4:16232800-16233610	K562	blood:	n/a	n/a
14	IRF1	chr4:16231118-16231285	K562	blood:	n/a	n/a
15	JUND	chr4:16230274-16230577	K562	blood:	n/a	n/a
16	MAFF	chr4:16232727-16232731	K562	blood:	n/a	n/a
17	MAFK	chr4:16230494-16230581	K562	blood:	n/a	n/a
18	MAZ	chr4:16230399-16230575	K562	blood:	n/a	n/a
19	MYC	chr4:16230055-16230113	K562	blood:	n/a	n/a
20	POLR2A	chr4:16231006-16231037	HepG2	liver:	n/a	n/a
21	POLR2A	chr4:16230218-16230244	MCF10A-Er-Src	breast:	n/a	n/a
22	POLR2A	chr4:16232660-16233905	MCF10A-Er-Src	breast:	n/a	n/a
23	POLR2A	chr4:16226783-16230420	Raji	blood:	n/a	n/a
24	POLR2A	chr4:16229922-16230322	K562	blood:	n/a	n/a
25	POLR2A	chr4:16230612-16230949	MCF10A-Er-Src	breast:	n/a	n/a
26	POLR2A	chr4:16231166-16231524	MCF10A-Er-Src	breast:	n/a	n/a
27	POLR2A	chr4:16230368-16230507	K562	blood:	n/a	n/a
28	POLR2A	chr4:16232075-16232240	MCF10A-Er-Src	breast:	n/a	n/a
29	POLR2A	chr4:16231131-16231494	GM12878	blood:	n/a	n/a
30	POLR2A	chr4:16232234-16232430	HepG2	liver:	n/a	n/a
31	POLR2A	chr4:16226639-16229966	PBDE	blood:	n/a	n/a
32	POLR2A	chr4:16228635-16234024	K562	blood:	n/a	n/a
33	POLR2A	chr4:16230349-16232360	MCF10A-Er-Src	breast:	n/a	n/a
34	POLR2A	chr4:16231811-16231828	MCF10A-Er-Src	breast:	n/a	n/a
35	POLR2A	chr4:16229991-16230145	K562	blood:	n/a	n/a
36	POLR2A	chr4:16226421-16229959	MCF10A-Er-Src	breast:	n/a	n/a
37	RCOR1	chr4:16230338-16230513	K562	blood:	n/a	n/a
38	RCOR1	chr4:16229879-16230079	K562	blood:	n/a	n/a
39	RFX5	chr4:16230717-16230777	K562	blood:	n/a	n/a
40	SPI1	chr4:16230156-16230549	HL-60	blood:	n/a	n/a
41	SPI1	chr4:16230316-16230445	K562	blood:	n/a	n/a
42	TBL1XR1	chr4:16230613-16230809	K562	blood:	n/a	n/a
43	TBP	chr4:16229823-16230428	K562	blood:	n/a	n/a
44	UBTF	chr4:16227439-16230550	K562	blood:	n/a	n/a
45	YY1	chr4:16229994-16230312	K562	blood:	n/a	n/a
46	YY1	chr4:16229964-16230325	K562	blood:	n/a	n/a
47	YY1	chr4:16230338-16230479	GM12878	blood:	n/a	n/a
48	ZNF384	chr4:16230193-16230559	GM12878	blood:	n/a	n/a
49	ZNF384	chr4:16229881-16230885	K562	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:16230109-16230159	SAEC	small airway:	n/a
2	chr4:16230109-16230159	HRCEpiC	kidney:	n/a
3	chr4:16230109-16230159	HRE	kidney:	n/a
4	chr4:16230109-16230159	Jurkat	blood:	n/a
5	chr4:16232771-16232821	HRE	kidney:	n/a
6	chr4:16230109-16230159	SK-N-SH_RA	brain:	n/a
7	chr4:16232771-16232821	ovcar-3	ovarian:	n/a
8	chr4:16232771-16232821	HL-60	blood:	n/a
9	chr4:16230109-16230159	PrEC	prostate:	n/a
10	chr4:16232771-16232821	SK-N-MC	brain:	n/a
11	chr4:16232771-16232821	MCF-7	breast:	n/a
12	chr4:16230109-16230159	HCT-116	colon:	n/a
13	chr4:16230109-16230159	IMR90	lung:	fetal
14	chr4:16230109-16230159	HUVEC	blood vessel:	n/a
15	chr4:16230109-16230159	LNCaP	prostate:	n/a
16	chr4:16230109-16230159	RPTEC	kidney:	n/a
17	chr4:16232771-16232821	MCF10A-Er-Src	breast:	n/a
18	chr4:16230109-16230159	Caco-2	colon:	n/a
19	chr4:16230109-16230159	AG09309	skin:	n/a
20	chr4:16232771-16232821	AG09309	skin:	n/a
21	chr4:16230109-16230159	ProgFib	skin:	n/a
22	chr4:16232771-16232821	GM19239	blood:	n/a
23	chr4:16230109-16230159	HCPEpiC	choroid plexus:	n/a
24	chr4:16230109-16230159	HEEpiC	esophagus:	n/a
25	chr4:16230109-16230159	HepG2	liver:	n/a
26	chr4:16230109-16230159	AG04449	skin:	fetal
27	chr4:16232771-16232821	AG10803	skin:	n/a
28	chr4:16232771-16232821	HNPCEpiC	eye:	n/a
29	chr4:16232771-16232821	HCPEpiC	choroid plexus:	n/a
30	chr4:16230109-16230159	HMEC	breast:	n/a
31	chr4:16232771-16232821	PANC-1	pancreas:	n/a
32	chr4:16230109-16230159	HNPCEpiC	eye:	n/a
33	chr4:16232771-16232821	HCF	heart:	n/a
34	chr4:16232771-16232821	H1-hESC	embryonic stem cell:	embryo
35	chr4:16230109-16230159	NHBE	bronchial:	n/a
36	chr4:16232771-16232821	GM06990	blood:	n/a
37	chr4:16230109-16230159	ovcar-3	ovarian:	n/a
38	chr4:16230109-16230159	MCF10A-Er-Src	breast:	n/a
39	chr4:16232771-16232821	LNCaP	prostate:	n/a
40	chr4:16232771-16232821	HepG2	liver:	n/a
41	chr4:16232771-16232821	BJ	skin:	n/a
42	chr4:16230109-16230159	Hepatocyte	liver:	n/a
43	chr4:16232771-16232821	HEK293	kidney:	embryo
44	chr4:16232771-16232821	GM12892	blood:	n/a
45	chr4:16230109-16230159	HIPEpiC	eye:	n/a
46	chr4:16232771-16232821	HCM	heart:	n/a
47	chr4:16232771-16232821	HRCEpiC	kidney:	n/a
48	chr4:16230109-16230159	NT2-D1	testis:	n/a
49	chr4:16230109-16230159	T-47D	breast:	n/a
50	chr4:16232771-16232821	ECC-1	luminal epithelium:	n/a

No.	Distal block	Cell Line	Cell type
1	chr4:16230982..16233844-chr4:16235259..16238422,3	MCF-7	breast:
2	chr4:15002785..15006911-chr4:16226901..16230678,5	K562	blood:
3	chr4:16230488..16232179-chr4:16234227..16236390,2	MCF-7	breast:
4	chr4:16227416..16229454-chr4:16230827..16235422,5	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CD38-2	chr4:16228286-16230207	ENSG00000263327.2

Variant related genes	Relation type
TAPT1	TF binding region
TAPT1	CpG island
ENSG00000169762	chromatin interactions
ENSG00000263327	chromatin interactions
ENSG00000137449	chromatin interactions
ENSG00000247624	chromatin interactions

Extended variants
information (count: 114 )
Associated
traits (count: 52 )

Variant overlapped rSNPs/rCNVs (count:114 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs201992726	chr4:16229946-16229947	Active TSS Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
2	rs35777961	chr4:16229983-16229984	Active TSS Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS	TF binding region Chromatin interactive region lncRNA	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs12645055	chr4:16230002-16230003	Active TSS Weak transcription Enhancers Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region lncRNA	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs189113350	chr4:16230005-16230006	Active TSS Weak transcription Enhancers Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
5	rs575811889	chr4:16230017-16230018	Active TSS Weak transcription Enhancers Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
6	rs112833301	chr4:16230018-16230019	Active TSS Weak transcription Enhancers Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
7	rs542434680	chr4:16230021-16230022	Active TSS Weak transcription Enhancers Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
8	rs562403135	chr4:16230024-16230025	Active TSS Weak transcription Enhancers Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
9	rs10939657	chr4:16230037-16230038	Active TSS Weak transcription Enhancers Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region lncRNA	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs544949454	chr4:16230055-16230056	Active TSS Weak transcription Enhancers Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
11	rs145233279	chr4:16230070-16230071	Active TSS Weak transcription Enhancers Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
12	rs184001772	chr4:16230081-16230082	Active TSS Weak transcription Enhancers Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
13	rs547438721	chr4:16230084-16230085	Active TSS Weak transcription Enhancers Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
14	rs533538372	chr4:16230096-16230097	Active TSS Weak transcription Enhancers Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
15	rs78541211	chr4:16230121-16230122	Active TSS Weak transcription Enhancers Flanking Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
16	rs9684049	chr4:16230131-16230132	Active TSS Weak transcription Enhancers Flanking Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
17	rs529459370	chr4:16230140-16230141	Active TSS Weak transcription Enhancers Flanking Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
18	rs549605066	chr4:16230173-16230174	Active TSS Weak transcription Enhancers Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
19	rs149169344	chr4:16230212-16230213	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs180978049	chr4:16230234-16230235	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs543229266	chr4:16230255-16230256	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs571599844	chr4:16230274-16230275	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs573309171	chr4:16230281-16230282	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs371522479	chr4:16230283-16230284	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs76538414	chr4:16230319-16230320	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs535952171	chr4:16230330-16230331	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs6854630	chr4:16230335-16230336	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs368123063	chr4:16230336-16230337	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs111884199	chr4:16230370-16230371	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs71179689	chr4:16230374-16230375	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs115859686	chr4:16230375-16230376	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs200627682	chr4:16230378-16230379	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs554210999	chr4:16230400-16230401	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs186102269	chr4:16230420-16230421	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs556245558	chr4:16230422-16230423	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs118005165	chr4:16230454-16230455	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs143230413	chr4:16230477-16230478	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs544889843	chr4:16230480-16230481	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs112879911	chr4:16230526-16230527	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs565177040	chr4:16230541-16230542	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs565049702	chr4:16230545-16230546	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs571982578	chr4:16230551-16230552	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs114844702	chr4:16230591-16230592	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs80000630	chr4:16230641-16230642	Flanking Active TSS Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs529801312	chr4:16230681-16230682	Flanking Active TSS Weak transcription Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs549947306	chr4:16230684-16230685	Flanking Active TSS Weak transcription Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs563048208	chr4:16230726-16230727	Flanking Active TSS Weak transcription Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs140394592	chr4:16230816-16230817	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs551550230	chr4:16230827-16230828	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs530132286	chr4:16230940-16230941	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:52)

Disease	PMID	Source
Oral squamous cell carcinoma	17134496	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Wilms tumour	21544195	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
T-cell prolymphocytic leukemia	19278963	CNVD
Hodgkin''s lymphoma	17606441	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
Breast cancer	21858162	CNVD
small cell lung cancer	20016488	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Cancer	21183584	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Gastric cancer	21586687	CNVD
Breast cancer	17133270	CNVD
lymphocytic leukemia	21291569	CNVD
Breast cancer	16608533	CNVD
Non-small cell lung cancer	21829676	CNVD
Melanoma	20877625	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
early-passage human iPS cells	21368824	CNVD

Chromatin state (count:181 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:16225600-16230800	Active TSS	A549	lung
2	chr4:16225800-16230000	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
3	chr4:16226400-16230600	Active TSS	GM12878-XiMat	blood
4	chr4:16226600-16230000	Active TSS	Pancreatic Islets	Pancreatic Islet
5	chr4:16226600-16230800	Active TSS	K562	blood
6	chr4:16226800-16230000	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
7	chr4:16226800-16230600	Active TSS	Brain Anterior Caudate	brain
8	chr4:16227000-16230000	Active TSS	HUES6 Cell Line	embryonic stem cell
9	chr4:16227000-16230000	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
10	chr4:16227000-16230600	Active TSS	ES-I3 Cell Line	embryonic stem cell
11	chr4:16227000-16230600	Active TSS	Brain Cingulate Gyrus	brain
12	chr4:16227000-16230800	Active TSS	Rectal Mucosa Donor 29	rectum
13	chr4:16227200-16230600	Active TSS	Colonic Mucosa	Colon
14	chr4:16228600-16230600	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
15	chr4:16228800-16230000	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
16	chr4:16228800-16230600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
17	chr4:16228800-16230800	Flanking Active TSS	Primary B cells from cord blood	blood
18	chr4:16229000-16230000	Flanking Active TSS	Brain Inferior Temporal Lobe	brain
19	chr4:16229000-16230000	Flanking Active TSS	Duodenum Mucosa	Duodenum
20	chr4:16229200-16230200	Flanking Active TSS	Primary monocytes fromperipheralblood	blood
21	chr4:16229200-16230200	Flanking Active TSS	Primary B cells from peripheral blood	blood
22	chr4:16229200-16230200	Flanking Active TSS	Primary hematopoietic stem cells	blood
23	chr4:16229200-16230200	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
24	chr4:16229200-16230200	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
25	chr4:16229200-16230200	Flanking Active TSS	Brain Angular Gyrus	brain
26	chr4:16229200-16231000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
27	chr4:16229400-16230000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
28	chr4:16229400-16230200	Enhancers	Primary T cells fromperipheralblood	blood
29	chr4:16229400-16230200	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
30	chr4:16229400-16230600	Enhancers	Primary T killer memory cells from peripheral blood	blood
31	chr4:16229400-16231600	Weak transcription	Sigmoid Colon	Sigmoid Colon
32	chr4:16229400-16241000	Weak transcription	Aorta	Aorta
33	chr4:16229600-16230000	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
34	chr4:16229600-16230000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
35	chr4:16229600-16230000	Active TSS	Fetal Brain Female	brain
36	chr4:16229600-16230000	Enhancers	Fetal Heart	heart
37	chr4:16229600-16230000	Bivalent Enhancer	Fetal Thymus	thymus
38	chr4:16229600-16230000	Enhancers	Dnd41	blood
39	chr4:16229600-16230200	Enhancers	Breast Myoepithelial Primary Cells	Breast
40	chr4:16229600-16230200	Enhancers	Primary T killer naive cells fromperipheralblood	blood
41	chr4:16229600-16230200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
42	chr4:16229600-16230200	Active TSS	Primary mononuclear cells fromperipheralblood	Blood
43	chr4:16229600-16230200	Enhancers	Fetal Brain Male	brain
44	chr4:16229600-16230200	Enhancers	Placenta	Placenta
45	chr4:16229600-16230200	Bivalent/Poised TSS	Thymus	Thymus
46	chr4:16229600-16230600	Enhancers	Liver	Liver
47	chr4:16229600-16233000	Weak transcription	Colon Smooth Muscle	Colon
48	chr4:16229600-16233200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
49	chr4:16229600-16233400	Weak transcription	Cortex derived primary cultured neurospheres	brain
50	chr4:16229600-16233400	Weak transcription	Right Atrium	heart

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