Variant report

Variant	nsv881310
Chromosome Location	chr4:172633978-172751522
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:315)
CpG islands
(count:795)
Chromatin interactive
region (count:18)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:315 , 50 per page) page: 1 2 3 4 5 6 7

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr4:172687302-172687374	K562	blood:	n/a	n/a
2	BACH1	chr4:172734531-172735200	H1-hESC	embryonic stem cell:	n/a	n/a
3	BCL11A	chr4:172672697-172672963	GM12878	blood:	n/a	n/a
4	BHLHE40	chr4:172672890-172673043	GM12878	blood:	n/a	n/a
5	CEBPB	chr4:172704852-172705072	A549	lung:	n/a	chr4:172704975-172704986
6	CEBPB	chr4:172636835-172637035	HepG2	liver:	n/a	chr4:172636946-172636957
7	CEBPB	chr4:172704898-172705046	H1-hESC	embryonic stem cell:	n/a	chr4:172704975-172704986
8	CEBPB	chr4:172641991-172642184	HepG2	liver:	n/a	n/a
9	CEBPB	chr4:172737988-172738245	HepG2	liver:	n/a	n/a
10	CEBPB	chr4:172704826-172705051	HepG2	liver:	n/a	chr4:172704975-172704986
11	CEBPB	chr4:172704807-172705157	IMR90	lung:	n/a	chr4:172704975-172704986
12	CEBPB	chr4:172704930-172704947	K562	blood:	n/a	n/a
13	CHD2	chr4:172734519-172734523	H1-hESC	embryonic stem cell:	n/a	n/a
14	CTBP2	chr4:172733621-172735351	H1-hESC	embryonic stem cell:	n/a	n/a
15	CTCF	chr4:172706620-172706770	GM12864	blood:	n/a	n/a
16	CTCF	chr4:172734640-172734790	SK-N-SH_RA	brain:	n/a	n/a
17	CTCF	chr4:172715871-172715909	MCF-7	breast:	n/a	n/a
18	CTCF	chr4:172706640-172706790	HBMEC	blood vessel:	n/a	n/a
19	CTCF	chr4:172734591-172734682	GM19239	blood:	n/a	n/a
20	CTCF	chr4:172706640-172706790	HRPEpiC	eye:	n/a	n/a
21	CTCF	chr4:172706654-172706834	LNCaP	prostate:	n/a	n/a
22	CTCF	chr4:172706620-172706770	WERI-Rb-1	eye:	n/a	n/a
23	CTCF	chr4:172715764-172716039	GM12878	blood:	n/a	n/a
24	CTCF	chr4:172706654-172706788	Spleen_OC	spleen:	n/a	n/a
25	CTCF	chr4:172715780-172715930	BE2_C	brain:	n/a	n/a
26	CTCF	chr4:172715720-172715870	HCT-116	colon:	n/a	n/a
27	CTCF	chr4:172715780-172715930	HEK293	kidney:	n/a	n/a
28	CTCF	chr4:172697500-172697650	HepG2	liver:	n/a	n/a
29	CTCF	chr4:172734221-172734317	MCF-7	breast:	n/a	n/a
30	CTCF	chr4:172706680-172706830	HMEC	breast:	n/a	n/a
31	CTCF	chr4:172734573-172734740	MCF-7	breast:	n/a	n/a
32	CTCF	chr4:172706698-172706794	GM10266	blood:	n/a	n/a
33	CTCF	chr4:172723038-172723065	GM20000	blood:	n/a	n/a
34	CTCF	chr4:172715875-172715938	MCF-7	breast:	n/a	n/a
35	CTCF	chr4:172734600-172734750	HCPEpiC	choroid plexus:	n/a	n/a
36	CTCF	chr4:172734607-172734703	MCF-7	breast:	n/a	n/a
37	CTCF	chr4:172706666-172706817	GM12878	blood:	n/a	n/a
38	CTCF	chr4:172706670-172706828	GM13977	blood:	n/a	n/a
39	CTCF	chr4:172706640-172706790	GM12871	blood:	n/a	n/a
40	CTCF	chr4:172734880-172735030	SK-N-SH_RA	brain:	n/a	n/a
41	CTCF	chr4:172706620-172706770	MCF-7	breast:	n/a	n/a
42	CTCF	chr4:172715820-172715970	WERI-Rb-1	eye:	n/a	n/a
43	CTCF	chr4:172661649-172661768	GM12878	blood:	n/a	n/a
44	CTCF	chr4:172729864-172729953	GM13976	blood:	n/a	n/a
45	CTCF	chr4:172706680-172706830	SK-N-SH_RA	brain:	n/a	n/a
46	CTCF	chr4:172715880-172715943	GM19240	blood:	n/a	n/a
47	CTCF	chr4:172706640-172706790	GM12873	blood:	n/a	n/a
48	CTCF	chr4:172706640-172706790	MCF-7	breast:	n/a	n/a
49	CTCF	chr4:172706640-172706790	AG04449	skin:	n/a	n/a
50	CTCF	chr4:172734140-172734290	AG04449	skin:	n/a	n/a

(count:795 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:172733566-172733616	NHBE	bronchial:	n/a
2	chr4:172735924-172735974	HCPEpiC	choroid plexus:	n/a
3	chr4:172733566-172733616	NHBE	bronchial:	n/a
4	chr4:172735924-172735974	HCPEpiC	choroid plexus:	n/a
5	chr4:172733566-172733616	LNCaP	prostate:	n/a
6	chr4:172734843-172734893	Hela-S3	cervix:	n/a
7	chr4:172734514-172734564	AG10803	skin:	n/a
8	chr4:172734031-172734081	MCF-7	breast:	n/a
9	chr4:172734266-172734316	PrEC	prostate:	n/a
10	chr4:172734843-172734893	HEK293	kidney:	embryo
11	chr4:172735924-172735974	NT2-D1	testis:	n/a
12	chr4:172734843-172734893	NHDF-neo	bronchial:	n/a
13	chr4:172734031-172734081	NHBE	bronchial:	n/a
14	chr4:172734776-172734826	HepG2	liver:	n/a
15	chr4:172734431-172734481	PFSK-1	brain:	n/a
16	chr4:172734431-172734481	SAEC	small airway:	n/a
17	chr4:172735924-172735974	NHBE	bronchial:	n/a
18	chr4:172735924-172735974	GM12878	blood:	n/a
19	chr4:172733760-172733810	SKMC	muscle:	n/a
20	chr4:172734266-172734316	SK-N-SH	brain:	n/a
21	chr4:172734276-172734326	NHBE	bronchial:	n/a
22	chr4:172734718-172734768	AG10803	skin:	n/a
23	chr4:172733566-172733616	IMR90	lung:	fetal
24	chr4:172734431-172734481	AG04449	skin:	fetal
25	chr4:172734266-172734316	NB4	blood:	n/a
26	chr4:172734843-172734893	HUVEC	blood vessel:	n/a
27	chr4:172734347-172734397	Jurkat	blood:	n/a
28	chr4:172734276-172734326	AoSMC	blood vessel:	n/a
29	chr4:172734507-172734557	BE2_C	brain:	n/a
30	chr4:172734718-172734768	GM12891	blood:	n/a
31	chr4:172734843-172734893	SK-N-MC	brain:	n/a
32	chr4:172734514-172734564	NH-A	brain:	n/a
33	chr4:172733760-172733810	HEK293	kidney:	embryo
34	chr4:172735924-172735974	RPTEC	kidney:	n/a
35	chr4:172734718-172734768	HIPEpiC	eye:	n/a
36	chr4:172734276-172734326	MCF10A-Er-Src	breast:	n/a
37	chr4:172734431-172734481	LNCaP	prostate:	n/a
38	chr4:172733760-172733810	HRCEpiC	kidney:	n/a
39	chr4:172734718-172734768	HEEpiC	esophagus:	n/a
40	chr4:172735924-172735974	HCM	heart:	n/a
41	chr4:172735924-172735974	HNPCEpiC	eye:	n/a
42	chr4:172733566-172733616	HUVEC	blood vessel:	n/a
43	chr4:172734276-172734326	HEK293	kidney:	embryo
44	chr4:172733760-172733810	NT2-D1	testis:	n/a
45	chr4:172734718-172734768	U87	brain:	n/a
46	chr4:172734718-172734768	H1-hESC	embryonic stem cell:	embryo
47	chr4:172734266-172734316	PANC-1	pancreas:	n/a
48	chr4:172734776-172734826	HCF	heart:	n/a
49	chr4:172734507-172734557	LNCaP	prostate:	n/a
50	chr4:172734347-172734397	SK-N-MC	brain:	n/a

(count:18 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:172729259..172730915-chr4:172731105..172733924,2	K562	blood:
2	chr4:172716048..172718001-chr4:172718061..172719826,2	K562	blood:
3	chr4:172716048..172718001-chr4:172718061..172719826,2	K562	blood:
4	chr4:172745393..172747896-chr4:172751501..172753836,2	K562	blood:
5	chr4:172734039..172736053-chr4:172737867..172739575,2	K562	blood:
6	chr4:172730871..172733159-chr4:172740265..172743202,2	K562	blood:
7	chr4:172745393..172747896-chr4:172751501..172753836,2	K562	blood:
8	chr4:172747937..172749943-chr4:172754889..172757555,2	K562	blood:
9	chr4:172734686..172736547-chr4:172736629..172739246,2	MCF-7	breast:
10	chr4:172734686..172736547-chr4:172736629..172739246,2	MCF-7	breast:
11	chr4:171797098..171797633-chr4:172706232..172706905,2	MCF-7	breast:
12	chr4:172736542..172738357-chr4:172740358..172742651,2	K562	blood:
13	chr4:171911858..171912761-chr4:172706205..172707181,4	MCF-7	breast:
14	chr4:172736542..172738357-chr4:172740358..172742651,2	K562	blood:
15	chr4:172107475..172108527-chr4:172706281..172707121,4	MCF-7	breast:
16	chr4:172729094..172730915-chr4:172731105..172733720,2	K562	blood:
17	chr4:171180937..171181444-chr4:172706313..172707200,2	MCF-7	breast:
18	chr4:172730871..172733159-chr4:172740265..172743202,2	K562	blood:

(count:3 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GALNT7-4	chr4:172734674-172735141	NONHSAT099205
2	lnc-GALNT7-4	chr4:172737189-172737342	NONHSAT099205
3	lnc-GALNT7-4	chr4:172735563-172735869	NONHSAT099205

No data

Variant related genes	Relation type
GALNTL6	TF binding region
GALNTL6	CpG island
ENSG00000174473	chromatin interactions

Extended variants
information (count: 1657 )
Associated
traits (count: 75 )

Variant overlapped rSNPs/rCNVs (count:1657 , 50 per page) page: 1 2 3 4 5 6 7 ... 34

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs9993484	chr4:172633978-172633979	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs548628388	chr4:172634053-172634054	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs189957755	chr4:172634090-172634091	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs142381387	chr4:172634101-172634102	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs117290721	chr4:172634191-172634192	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs570924990	chr4:172634218-172634219	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs146372527	chr4:172634221-172634222	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs551540692	chr4:172634250-172634251	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs117580480	chr4:172634251-172634252	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs567411754	chr4:172634305-172634306	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs536046347	chr4:172634325-172634326	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs545142196	chr4:172634347-172634348	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs556446820	chr4:172634355-172634356	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs576586348	chr4:172634379-172634380	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs539172358	chr4:172634418-172634419	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs565136275	chr4:172634469-172634470	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs558960232	chr4:172634476-172634477	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs571328540	chr4:172634480-172634481	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs2643420	chr4:172634547-172634548	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs2643419	chr4:172634554-172634555	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs561434049	chr4:172634568-172634569	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs370635849	chr4:172634585-172634586	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs575118204	chr4:172634606-172634607	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs562904881	chr4:172634611-172634612	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs543587513	chr4:172634745-172634746	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs563574533	chr4:172634785-172634786	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs531271629	chr4:172634829-172634830	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs181330949	chr4:172634858-172634859	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs116621205	chr4:172634901-172634902	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs185922427	chr4:172634904-172634905	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs527297026	chr4:172634908-172634909	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs547408042	chr4:172634913-172634914	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs567442138	chr4:172634951-172634952	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs188294223	chr4:172634982-172634983	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs549987801	chr4:172635001-172635002	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs372781062	chr4:172635004-172635005	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs370393229	chr4:172635005-172635006	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs569883208	chr4:172635035-172635036	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs181913270	chr4:172635067-172635068	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs186558448	chr4:172635073-172635074	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs138996635	chr4:172635078-172635079	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs141798120	chr4:172635084-172635085	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs554995124	chr4:172635099-172635100	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs114266644	chr4:172635101-172635102	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs567722390	chr4:172635110-172635111	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs190567963	chr4:172635142-172635143	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs557103427	chr4:172635153-172635154	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs577023405	chr4:172635154-172635155	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs544661627	chr4:172635176-172635177	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs150160832	chr4:172635180-172635181	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:75)

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
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
Wilms tumour	21544195	CNVD
Lung cancer	18438408	CNVD
Cancer	22429812	CNVD
Acute lymphoblastic leukemia	20435627	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
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
Ewing''s sarcoma	17952124	CNVD
Breast cancer	21633010	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Cancer	20581869	CNVD
Hepatocellular carcinoma	16750200	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
abnormal development	18461090	CNVD
Esophageal squamous carcinoma	17470683	CNVD
Neuroblastoma	16790693	CNVD
Schizophrenia	23813976	CNVD
Lung cancer	16773561	CNVD
Colorectal cancer	16774939	CNVD
Myelofibrosis	22110671	CNVD
Developmental delay	22127048	CNVD
Glioblastoma multiforme	22286061	CNVD
Neuroblastoma	21899760	CNVD
Gastric adenocarcinoma	19115996	CNVD
Urothelial carcinoma	21177765	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Prostate cancer	22341455	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:344 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:172631000-172636000	Weak transcription	Gastric	stomach
2	chr4:172632400-172642600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
3	chr4:172636000-172637400	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
4	chr4:172636000-172637400	ZNF genes & repeats	Gastric	stomach
5	chr4:172636200-172636800	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
6	chr4:172639200-172639600	Enhancers	Breast Myoepithelial Primary Cells	Breast
7	chr4:172639400-172640200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
8	chr4:172639800-172640400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
9	chr4:172653800-172654000	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
10	chr4:172654000-172654400	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
11	chr4:172654400-172654600	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
12	chr4:172663200-172663800	Enhancers	Brain Hippocampus Middle	brain
13	chr4:172677200-172678400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
14	chr4:172680200-172680600	Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
15	chr4:172680400-172680600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
16	chr4:172688600-172689000	Enhancers	HUES48 Cell Line	embryonic stem cell
17	chr4:172695600-172695800	Enhancers	Fetal Brain Male	brain
18	chr4:172695800-172696600	Weak transcription	Fetal Brain Male	brain
19	chr4:172696600-172697400	Enhancers	Fetal Brain Male	brain
20	chr4:172701200-172704200	Weak transcription	Right Atrium	heart
21	chr4:172704200-172704400	ZNF genes & repeats	Right Atrium	heart
22	chr4:172704200-172705200	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
23	chr4:172714600-172714800	Enhancers	Pancreatic Islets	Pancreatic Islet
24	chr4:172714600-172715000	Enhancers	Skeletal Muscle Male	skeletal muscle
25	chr4:172715000-172715600	Weak transcription	Pancreatic Islets	Pancreatic Islet
26	chr4:172715600-172715800	Enhancers	Pancreatic Islets	Pancreatic Islet
27	chr4:172715800-172719400	Weak transcription	Pancreatic Islets	Pancreatic Islet
28	chr4:172725800-172726200	Enhancers	ES-I3 Cell Line	embryonic stem cell
29	chr4:172731400-172732400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
30	chr4:172733000-172733400	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
31	chr4:172733000-172734000	Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
32	chr4:172733200-172733400	Bivalent/Poised TSS	Primary hematopoietic stem cells	blood
33	chr4:172733200-172733400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
34	chr4:172733200-172733600	Active TSS	Brain Anterior Caudate	brain
35	chr4:172733200-172737200	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
36	chr4:172733400-172733600	Bivalent/Poised TSS	H1 Cell Line	embryonic stem cell
37	chr4:172733400-172733600	Bivalent Enhancer	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
38	chr4:172733400-172733600	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
39	chr4:172733400-172733600	Flanking Bivalent TSS/Enh	HUES64 Cell Line	embryonic stem cell
40	chr4:172733400-172733600	Flanking Bivalent TSS/Enh	iPS-15b Cell Line	embryonic stem cell
41	chr4:172733400-172733600	Flanking Bivalent TSS/Enh	iPS-18 Cell Line	embryonic stem cell
42	chr4:172733400-172733600	Active TSS	Primary B cells from cord blood	blood
43	chr4:172733400-172733600	Bivalent/Poised TSS	Ganglion Eminence derived primary cultured neurospheres	brain
44	chr4:172733400-172733600	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
45	chr4:172733400-172733600	Bivalent Enhancer	Adipose Nuclei	Adipose
46	chr4:172733400-172733600	Active TSS	Brain Angular Gyrus	brain
47	chr4:172733400-172733600	Active TSS	Brain Cingulate Gyrus	brain
48	chr4:172733400-172733600	Active TSS	Brain Inferior Temporal Lobe	brain
49	chr4:172733400-172733600	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
50	chr4:172733400-172733600	Flanking Bivalent TSS/Enh	Fetal Kidney	kidney

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