Variant report

Variant	nsv1000404
Chromosome Location	chr4:16338191-16363909
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:59)
CpG islands
(count:430)
Chromatin interactive
region (count:8)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:59 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CHD2	chr4:16362360-16362692	K562	blood:	n/a	n/a
2	E2F4	chr4:16363661-16363799	MCF10A-Er-Src	breast:	n/a	n/a
3	E2F4	chr4:16360641-16360852	MCF10A-Er-Src	breast:	n/a	n/a
4	E2F4	chr4:16339574-16339817	MCF10A-Er-Src	breast:	n/a	n/a
5	E2F6	chr4:16362597-16362767	K562	blood:	n/a	n/a
6	ELF1	chr4:16362212-16362798	MCF-7	breast:	n/a	n/a
7	ELF1	chr4:16362289-16362761	MCF-7	breast:	n/a	n/a
8	EP300	chr4:16339578-16340079	ECC-1	luminal epithelium:	n/a	chr4:16339606-16339615
9	FOS	chr4:16339471-16339936	MCF10A-Er-Src	breast:	n/a	chr4:16339607-16339615 chr4:16339605-16339617 chr4:16339607-16339615 chr4:16339608-16339615
10	FOS	chr4:16339479-16339925	MCF10A-Er-Src	breast:	n/a	chr4:16339607-16339615 chr4:16339605-16339617 chr4:16339607-16339615 chr4:16339608-16339615
11	FOS	chr4:16339529-16339883	MCF10A-Er-Src	breast:	n/a	chr4:16339607-16339615 chr4:16339605-16339617 chr4:16339607-16339615 chr4:16339608-16339615
12	FOS	chr4:16339477-16339919	MCF10A-Er-Src	breast:	n/a	chr4:16339607-16339615 chr4:16339605-16339617 chr4:16339607-16339615 chr4:16339608-16339615
13	HA-E2F1	chr4:16362306-16363059	MCF-7	breast:	n/a	n/a
14	IRF1	chr4:16357311-16357460	K562	blood:	n/a	n/a
15	MAFF	chr4:16348525-16348762	HepG2	liver:	n/a	n/a
16	MAFK	chr4:16348561-16348761	HepG2	liver:	n/a	n/a
17	MAFK	chr4:16346479-16346552	HepG2	liver:	n/a	n/a
18	MAFK	chr4:16348552-16348793	HepG2	liver:	n/a	n/a
19	MAX	chr4:16362445-16362769	MCF-7	breast:	n/a	n/a
20	MAX	chr4:16362167-16362522	K562	blood:	n/a	n/a
21	MAX	chr4:16354947-16355115	NB4	blood:	n/a	chr4:16354987-16354997
22	MYC	chr4:16339630-16339719	MCF10A-Er-Src	breast:	n/a	n/a
23	MYC	chr4:16362427-16362723	MCF-7	breast:	n/a	n/a
24	MYC	chr4:16362429-16362626	H1-hESC	embryonic stem cell:	n/a	n/a
25	MYC	chr4:16362408-16362824	MCF-7	breast:	n/a	n/a
26	MYC	chr4:16345444-16345447	MCF10A-Er-Src	breast:	n/a	n/a
27	MYC	chr4:16362417-16362669	MCF-7	breast:	n/a	n/a
28	PML	chr4:16362453-16362761	MCF-7	breast:	n/a	n/a
29	POLR2A	chr4:16362508-16362535	ProgFib	skin:	n/a	n/a
30	POLR2A	chr4:16338261-16338296	MCF10A-Er-Src	breast:	n/a	n/a
31	POLR2A	chr4:16362561-16362776	ProgFib	skin:	n/a	n/a
32	POLR2A	chr4:16362130-16363282	MCF-7	breast:	n/a	n/a
33	POLR2A	chr4:16362334-16362650	K562	blood:	n/a	n/a
34	POLR2A	chr4:16362271-16362913	MCF-7	breast:	n/a	n/a
35	POLR2A	chr4:16344102-16344244	MCF10A-Er-Src	breast:	n/a	n/a
36	POLR2A	chr4:16359970-16360061	K562	blood:	n/a	n/a
37	POLR2A	chr4:16362252-16362898	MCF-7	breast:	n/a	n/a
38	POLR2A	chr4:16338940-16338946	MCF10A-Er-Src	breast:	n/a	n/a
39	POLR2A	chr4:16354902-16355014	ProgFib	skin:	n/a	n/a
40	POLR2A	chr4:16362267-16362328	K562	blood:	n/a	n/a
41	POLR2A	chr4:16353183-16353327	MCF10A-Er-Src	breast:	n/a	n/a
42	POLR2A	chr4:16362107-16362125	MCF-7	breast:	n/a	n/a
43	SPI1	chr4:16351828-16352357	HL-60	blood:	n/a	chr4:16352067-16352076 chr4:16352065-16352078 chr4:16352066-16352079 chr4:16352068-16352075
44	SPI1	chr4:16351942-16352161	HL-60	blood:	n/a	chr4:16352067-16352076 chr4:16352065-16352078 chr4:16352066-16352079 chr4:16352068-16352075
45	SPI1	chr4:16351981-16352131	K562	blood:	n/a	chr4:16352067-16352076 chr4:16352065-16352078 chr4:16352066-16352079 chr4:16352068-16352075
46	SPI1	chr4:16350375-16350792	HL-60	blood:	n/a	n/a
47	STAT3	chr4:16346598-16346719	MCF10A-Er-Src	breast:	n/a	n/a
48	STAT3	chr4:16339530-16339894	MCF10A-Er-Src	breast:	n/a	n/a
49	STAT3	chr4:16339571-16339820	MCF10A-Er-Src	breast:	n/a	n/a
50	STAT3	chr4:16347199-16347317	MCF10A-Er-Src	breast:	n/a	n/a

(count:430 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:16362584-16362634	BJ	skin:	n/a
2	chr4:16362664-16362714	NHDF-neo	bronchial:	n/a
3	chr4:16363266-16363316	AoSMC	blood vessel:	n/a
4	chr4:16362584-16362634	BJ	skin:	n/a
5	chr4:16362664-16362714	NHDF-neo	bronchial:	n/a
6	chr4:16363266-16363316	AoSMC	blood vessel:	n/a
7	chr4:16359846-16359896	PANC-1	pancreas:	n/a
8	chr4:16362664-16362714	NHBE	bronchial:	n/a
9	chr4:16362340-16362390	H1-hESC	embryonic stem cell:	embryo
10	chr4:16362664-16362714	HAEpiC	amniotic membrane:	n/a
11	chr4:16362584-16362634	HCT-116	colon:	n/a
12	chr4:16362584-16362634	GM12892	blood:	n/a
13	chr4:16362584-16362634	HEK293	kidney:	embryo
14	chr4:16362422-16362472	HEK293	kidney:	embryo
15	chr4:16363266-16363316	Hepatocyte	liver:	n/a
16	chr4:16362584-16362634	GM19239	blood:	n/a
17	chr4:16362422-16362472	NHBE	bronchial:	n/a
18	chr4:16359846-16359896	HNPCEpiC	eye:	n/a
19	chr4:16362664-16362714	AG10803	skin:	n/a
20	chr4:16362666-16362716	SK-N-SH_RA	brain:	n/a
21	chr4:16362422-16362472	GM12892	blood:	n/a
22	chr4:16362584-16362634	IMR90	lung:	fetal
23	chr4:16362664-16362714	AG09319	gingival:	n/a
24	chr4:16362666-16362716	GM19239	blood:	n/a
25	chr4:16359846-16359896	Caco-2	colon:	n/a
26	chr4:16362340-16362390	Hela-S3	cervix:	n/a
27	chr4:16362584-16362634	HCPEpiC	choroid plexus:	n/a
28	chr4:16362340-16362390	T-47D	breast:	n/a
29	chr4:16362340-16362390	HUVEC	blood vessel:	n/a
30	chr4:16362664-16362714	HIPEpiC	eye:	n/a
31	chr4:16359846-16359896	ECC-1	luminal epithelium:	n/a
32	chr4:16362666-16362716	HRE	kidney:	n/a
33	chr4:16362664-16362714	HMEC	breast:	n/a
34	chr4:16362422-16362472	IMR90	lung:	fetal
35	chr4:16362666-16362716	AG09319	gingival:	n/a
36	chr4:16363266-16363316	NT2-D1	testis:	n/a
37	chr4:16362666-16362716	HCPEpiC	choroid plexus:	n/a
38	chr4:16362664-16362714	RPTEC	kidney:	n/a
39	chr4:16362664-16362714	HEEpiC	esophagus:	n/a
40	chr4:16362422-16362472	HRE	kidney:	n/a
41	chr4:16362664-16362714	Hela-S3	cervix:	n/a
42	chr4:16362666-16362716	ECC-1	luminal epithelium:	n/a
43	chr4:16362666-16362716	Hepatocyte	liver:	n/a
44	chr4:16362422-16362472	HAEpiC	amniotic membrane:	n/a
45	chr4:16359846-16359896	CMK	blood:	n/a
46	chr4:16363266-16363316	MCF-7	breast:	n/a
47	chr4:16362664-16362714	HEK293	kidney:	embryo
48	chr4:16362584-16362634	SAEC	small airway:	n/a
49	chr4:16362666-16362716	HAEpiC	amniotic membrane:	n/a
50	chr4:16362340-16362390	HNPCEpiC	eye:	n/a

(count:8 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:16360699..16362829-chr4:16383139..16385452,2	MCF-7	breast:
2	chr4:16355873..16357763-chr4:16357802..16360791,2	MCF-7	breast:
3	chr4:16355873..16357763-chr4:16357802..16360791,2	MCF-7	breast:
4	chr19:56161626..56162436-chr4:16357679..16358532,2	MCF-7	breast:
5	chr4:16320021..16320816-chr4:16349710..16350236,2	MCF-7	breast:
6	chr4:16355756..16359124-chr4:16361383..16363978,4	MCF-7	breast:
7	chr4:16331798..16335655-chr4:16340723..16344531,3	K562	blood:
8	chr4:16258640..16260295-chr4:16352186..16354704,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TAPT1-3	chr4:16362507-16362611	NONHSAT095687
2	lnc-CD38-2	chr4:16357243-16357365	XLOC_003469
3	lnc-CD38-2	chr4:16357242-16357365	NONHSAT095684

No data

Variant related genes	Relation type
ZEB2P1	TF binding region
ZEB2P1	CpG island
ENSG00000249506	chromatin interactions

Extended variants
information (count: 748 )
Associated
traits (count: 51 )

Variant overlapped rSNPs/rCNVs (count:748 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs148065491	chr4:16338223-16338224	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs192660019	chr4:16338241-16338242	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs542175242	chr4:16338244-16338245	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs141722684	chr4:16338261-16338262	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs540203303	chr4:16338323-16338324	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs372787581	chr4:16338330-16338331	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs535251778	chr4:16338349-16338350	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs559670636	chr4:16338370-16338371	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs150574016	chr4:16338411-16338412	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
10	rs73239730	chr4:16338447-16338448	ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs562265355	chr4:16338544-16338545	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
12	rs531341749	chr4:16338555-16338556	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
13	rs11736850	chr4:16338574-16338575	ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs564572993	chr4:16338576-16338577	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
15	rs533628303	chr4:16338577-16338578	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
16	rs184452659	chr4:16338581-16338582	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
17	rs566840306	chr4:16338653-16338654	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs529329720	chr4:16338692-16338693	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs550630979	chr4:16338721-16338722	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs549428784	chr4:16338843-16338844	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs372888721	chr4:16338847-16338848	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs190612489	chr4:16338852-16338853	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs578098807	chr4:16338857-16338858	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs112109792	chr4:16338873-16338874	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs537991597	chr4:16338908-16338909	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs557927917	chr4:16338962-16338963	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs182313567	chr4:16339020-16339021	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs73239731	chr4:16339033-16339034	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs62296749	chr4:16339038-16339039	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs560337776	chr4:16339066-16339067	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs184387165	chr4:16339078-16339079	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs189093545	chr4:16339180-16339181	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs181168817	chr4:16339189-16339190	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs146107063	chr4:16339234-16339235	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs4698469	chr4:16339238-16339239	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs56754521	chr4:16339242-16339243	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs555781110	chr4:16339249-16339250	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs73239732	chr4:16339293-16339294	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs544782110	chr4:16339342-16339343	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs373258867	chr4:16339350-16339351	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs189732594	chr4:16339368-16339369	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs180810895	chr4:16339399-16339400	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs533380024	chr4:16339406-16339407	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs372561193	chr4:16339416-16339417	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs374839504	chr4:16339418-16339419	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs369481456	chr4:16339419-16339420	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs386399367	chr4:16339427-16339428	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs397726314	chr4:16339428-16339429	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs141589361	chr4:16339432-16339433	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs567447171	chr4:16339442-16339443	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:51)

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

Chromatin state (count:51 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:16335400-16338400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr4:16338400-16338600	ZNF genes & repeats	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
3	chr4:16338600-16353200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
4	chr4:16339800-16340200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
5	chr4:16339800-16340200	Enhancers	NH-A	brain
6	chr4:16339800-16340200	Enhancers	NHEK	skin
7	chr4:16339800-16341000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
8	chr4:16349800-16350000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
9	chr4:16350000-16352800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
10	chr4:16350200-16350600	Enhancers	Spleen	Spleen
11	chr4:16351400-16351600	Enhancers	iPS-20b Cell Line	embryonic stem cell
12	chr4:16351400-16354000	Enhancers	HUES64 Cell Line	embryonic stem cell
13	chr4:16351600-16351800	Enhancers	HUES48 Cell Line	embryonic stem cell
14	chr4:16351600-16351800	Enhancers	HUES6 Cell Line	embryonic stem cell
15	chr4:16351600-16351800	Enhancers	iPS-18 Cell Line	embryonic stem cell
16	chr4:16351600-16352200	Enhancers	iPS-15b Cell Line	embryonic stem cell
17	chr4:16351600-16352200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
18	chr4:16351800-16352800	Weak transcription	HUES48 Cell Line	embryonic stem cell
19	chr4:16351800-16353000	Weak transcription	HUES6 Cell Line	embryonic stem cell
20	chr4:16352000-16353000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
21	chr4:16352200-16352600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
22	chr4:16352200-16353000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
23	chr4:16352200-16353200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
24	chr4:16352200-16353800	Enhancers	Brain Germinal Matrix	brain
25	chr4:16352600-16355000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
26	chr4:16352800-16353800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
27	chr4:16352800-16353800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
28	chr4:16352800-16353800	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
29	chr4:16352800-16353800	Enhancers	HUES48 Cell Line	embryonic stem cell
30	chr4:16352800-16353800	Enhancers	Fetal Brain Female	brain
31	chr4:16353000-16353600	Enhancers	iPS-18 Cell Line	embryonic stem cell
32	chr4:16353000-16353800	Enhancers	HUES6 Cell Line	embryonic stem cell
33	chr4:16353000-16353800	Enhancers	iPS-20b Cell Line	embryonic stem cell
34	chr4:16353000-16353800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
35	chr4:16353000-16353800	Enhancers	Cortex derived primary cultured neurospheres	brain
36	chr4:16353000-16353800	Enhancers	Brain Cingulate Gyrus	brain
37	chr4:16353200-16353400	Enhancers	iPS-15b Cell Line	embryonic stem cell
38	chr4:16353200-16353800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
39	chr4:16353200-16353800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
40	chr4:16353200-16353800	Enhancers	Brain Substantia Nigra	brain
41	chr4:16353400-16353800	Enhancers	Brain Hippocampus Middle	brain
42	chr4:16353800-16354600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
43	chr4:16353800-16355000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
44	chr4:16354800-16355000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
45	chr4:16355000-16355200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
46	chr4:16357200-16358400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
47	chr4:16359200-16359600	Enhancers	Fetal Stomach	stomach
48	chr4:16362200-16362600	Active TSS	K562	blood
49	chr4:16362400-16363000	Active TSS	Placenta	Placenta
50	chr4:16362400-16363200	ZNF genes & repeats	Pancreas	Pancrea

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