Variant report

Variant	nsv999436
Chromosome Location	chr4:16335379-16375164
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:68)
CpG islands
(count:488)
Chromatin interactive
region (count:13)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:68 , 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	CTCF	chr4:16374276-16374380	LNCaP	prostate:	n/a	n/a
3	E2F4	chr4:16366375-16366575	MCF10A-Er-Src	breast:	n/a	n/a
4	E2F4	chr4:16339574-16339817	MCF10A-Er-Src	breast:	n/a	n/a
5	E2F4	chr4:16363661-16363799	MCF10A-Er-Src	breast:	n/a	n/a
6	E2F4	chr4:16360641-16360852	MCF10A-Er-Src	breast:	n/a	n/a
7	E2F6	chr4:16362597-16362767	K562	blood:	n/a	n/a
8	ELF1	chr4:16362289-16362761	MCF-7	breast:	n/a	n/a
9	ELF1	chr4:16362212-16362798	MCF-7	breast:	n/a	n/a
10	EP300	chr4:16339578-16340079	ECC-1	luminal epithelium:	n/a	chr4:16339606-16339615
11	FAM48A	chr4:16336792-16336988	GM12878	blood:	n/a	n/a
12	FOS	chr4:16339529-16339883	MCF10A-Er-Src	breast:	n/a	chr4:16339607-16339615 chr4:16339605-16339617 chr4:16339607-16339615 chr4:16339608-16339615
13	FOS	chr4:16339477-16339919	MCF10A-Er-Src	breast:	n/a	chr4:16339607-16339615 chr4:16339605-16339617 chr4:16339607-16339615 chr4:16339608-16339615
14	FOS	chr4:16339471-16339936	MCF10A-Er-Src	breast:	n/a	chr4:16339607-16339615 chr4:16339605-16339617 chr4:16339607-16339615 chr4:16339608-16339615
15	FOS	chr4:16339479-16339925	MCF10A-Er-Src	breast:	n/a	chr4:16339607-16339615 chr4:16339605-16339617 chr4:16339607-16339615 chr4:16339608-16339615
16	HA-E2F1	chr4:16362306-16363059	MCF-7	breast:	n/a	n/a
17	IRF1	chr4:16357311-16357460	K562	blood:	n/a	n/a
18	MAFF	chr4:16348525-16348762	HepG2	liver:	n/a	n/a
19	MAFK	chr4:16348561-16348761	HepG2	liver:	n/a	n/a
20	MAFK	chr4:16346479-16346552	HepG2	liver:	n/a	n/a
21	MAFK	chr4:16367690-16367765	HepG2	liver:	n/a	n/a
22	MAFK	chr4:16348552-16348793	HepG2	liver:	n/a	n/a
23	MAX	chr4:16362445-16362769	MCF-7	breast:	n/a	n/a
24	MAX	chr4:16354947-16355115	NB4	blood:	n/a	chr4:16354987-16354997
25	MAX	chr4:16362167-16362522	K562	blood:	n/a	n/a
26	MYC	chr4:16362417-16362669	MCF-7	breast:	n/a	n/a
27	MYC	chr4:16362427-16362723	MCF-7	breast:	n/a	n/a
28	MYC	chr4:16362408-16362824	MCF-7	breast:	n/a	n/a
29	MYC	chr4:16339630-16339719	MCF10A-Er-Src	breast:	n/a	n/a
30	MYC	chr4:16362429-16362626	H1-hESC	embryonic stem cell:	n/a	n/a
31	MYC	chr4:16345444-16345447	MCF10A-Er-Src	breast:	n/a	n/a
32	PML	chr4:16362453-16362761	MCF-7	breast:	n/a	n/a
33	POLR2A	chr4:16338940-16338946	MCF10A-Er-Src	breast:	n/a	n/a
34	POLR2A	chr4:16353183-16353327	MCF10A-Er-Src	breast:	n/a	n/a
35	POLR2A	chr4:16362107-16362125	MCF-7	breast:	n/a	n/a
36	POLR2A	chr4:16362271-16362913	MCF-7	breast:	n/a	n/a
37	POLR2A	chr4:16368672-16368763	MCF10A-Er-Src	breast:	n/a	n/a
38	POLR2A	chr4:16362267-16362328	K562	blood:	n/a	n/a
39	POLR2A	chr4:16362130-16363282	MCF-7	breast:	n/a	n/a
40	POLR2A	chr4:16362561-16362776	ProgFib	skin:	n/a	n/a
41	POLR2A	chr4:16336236-16336684	SK-N-MC	brain:	n/a	n/a
42	POLR2A	chr4:16362252-16362898	MCF-7	breast:	n/a	n/a
43	POLR2A	chr4:16359970-16360061	K562	blood:	n/a	n/a
44	POLR2A	chr4:16366829-16367151	H1-neurons	neurons:	n/a	n/a
45	POLR2A	chr4:16362334-16362650	K562	blood:	n/a	n/a
46	POLR2A	chr4:16344102-16344244	MCF10A-Er-Src	breast:	n/a	n/a
47	POLR2A	chr4:16354902-16355014	ProgFib	skin:	n/a	n/a
48	POLR2A	chr4:16362508-16362535	ProgFib	skin:	n/a	n/a
49	POLR2A	chr4:16338261-16338296	MCF10A-Er-Src	breast:	n/a	n/a
50	POLR2A	chr4:16365781-16365862	MCF10A-Er-Src	breast:	n/a	n/a

(count:488 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:16363266-16363316	HRPEpiC	eye:	n/a
2	chr4:16366593-16366643	AG04449	skin:	fetal
3	chr4:16366593-16366643	SK-N-MC	brain:	n/a
4	chr4:16362584-16362634	NT2-D1	testis:	n/a
5	chr4:16362664-16362714	AoSMC	blood vessel:	n/a
6	chr4:16362666-16362716	SKMC	muscle:	n/a
7	chr4:16363266-16363316	HRE	kidney:	n/a
8	chr4:16366593-16366643	AoSMC	blood vessel:	n/a
9	chr4:16362422-16362472	ECC-1	luminal epithelium:	n/a
10	chr4:16362340-16362390	ovcar-3	ovarian:	n/a
11	chr4:16362666-16362716	HAEpiC	amniotic membrane:	n/a
12	chr4:16362664-16362714	HAEpiC	amniotic membrane:	n/a
13	chr4:16362584-16362634	AG09319	gingival:	n/a
14	chr4:16366593-16366643	HRCEpiC	kidney:	n/a
15	chr4:16362666-16362716	AG09309	skin:	n/a
16	chr4:16362584-16362634	NB4	blood:	n/a
17	chr4:16362422-16362472	Hepatocyte	liver:	n/a
18	chr4:16362340-16362390	CMK	blood:	n/a
19	chr4:16363266-16363316	RPTEC	kidney:	n/a
20	chr4:16362666-16362716	T-47D	breast:	n/a
21	chr4:16366593-16366643	GM06990	blood:	n/a
22	chr4:16362584-16362634	HCPEpiC	choroid plexus:	n/a
23	chr4:16363266-16363316	HPAEpiC	pulmonary alveolar:	n/a
24	chr4:16362664-16362714	Hela-S3	cervix:	n/a
25	chr4:16362584-16362634	H1-hESC	embryonic stem cell:	embryo
26	chr4:16362340-16362390	ECC-1	luminal epithelium:	n/a
27	chr4:16362422-16362472	SKMC	muscle:	n/a
28	chr4:16362422-16362472	H1-hESC	embryonic stem cell:	embryo
29	chr4:16363266-16363316	AG10803	skin:	n/a
30	chr4:16359846-16359896	AG09309	skin:	n/a
31	chr4:16362664-16362714	HEEpiC	esophagus:	n/a
32	chr4:16362584-16362634	NHDF-neo	bronchial:	n/a
33	chr4:16363266-16363316	SAEC	small airway:	n/a
34	chr4:16362422-16362472	BJ	skin:	n/a
35	chr4:16363266-16363316	AG09319	gingival:	n/a
36	chr4:16362666-16362716	PFSK-1	brain:	n/a
37	chr4:16362666-16362716	HCM	heart:	n/a
38	chr4:16362340-16362390	PrEC	prostate:	n/a
39	chr4:16362664-16362714	HUVEC	blood vessel:	n/a
40	chr4:16359846-16359896	HRCEpiC	kidney:	n/a
41	chr4:16362340-16362390	IMR90	lung:	fetal
42	chr4:16359846-16359896	RPTEC	kidney:	n/a
43	chr4:16359846-16359896	HUVEC	blood vessel:	n/a
44	chr4:16363266-16363316	HEEpiC	esophagus:	n/a
45	chr4:16359846-16359896	AG09319	gingival:	n/a
46	chr4:16366593-16366643	IMR90	lung:	fetal
47	chr4:16366593-16366643	Caco-2	colon:	n/a
48	chr4:16362584-16362634	NH-A	brain:	n/a
49	chr4:16359846-16359896	K562	blood:	n/a
50	chr4:16359846-16359896	MCF10A-Er-Src	breast:	n/a

(count:13 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:16258640..16260295-chr4:16352186..16354704,2	K562	blood:
2	chr4:16355756..16359124-chr4:16361383..16363978,4	MCF-7	breast:
3	chr4:16363037..16365847-chr4:16366056..16368462,2	K562	blood:
4	chr4:16320021..16320816-chr4:16349710..16350236,2	MCF-7	breast:
5	chr4:16331798..16335655-chr4:16340723..16344531,3	K562	blood:
6	chr4:16360973..16364086-chr4:16365820..16368451,4	MCF-7	breast:
7	chr4:16360699..16362829-chr4:16383139..16385452,2	MCF-7	breast:
8	chr4:16355873..16357763-chr4:16357802..16360791,2	MCF-7	breast:
9	chr19:56161626..56162436-chr4:16357679..16358532,2	MCF-7	breast:
10	chr4:16364655..16366735-chr4:16377619..16379236,2	K562	blood:
11	chr4:16331798..16335655-chr4:16340723..16344531,3	K562	blood:
12	chr4:16355873..16357763-chr4:16357802..16360791,2	MCF-7	breast:
13	chr4:16361224..16363467-chr4:16364801..16367359,3	MCF-7	breast:

(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	chr4:16357242-16357365	NONHSAT095684
3	lnc-CD38-2	chr4:16357243-16357365	XLOC_003469

No data

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

Extended variants
information (count: 990 )
Associated
traits (count: 51 )

Variant overlapped rSNPs/rCNVs (count:990 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11736183	chr4:16335379-16335380	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs546286181	chr4:16335404-16335405	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs560902384	chr4:16335407-16335408	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs574503163	chr4:16335408-16335409	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs34253907	chr4:16335421-16335422	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs548175361	chr4:16335436-16335437	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs543474988	chr4:16335490-16335491	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs76750891	chr4:16335509-16335510	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs190219407	chr4:16335674-16335675	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs375897675	chr4:16335690-16335691	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs370531635	chr4:16335713-16335714	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs149934553	chr4:16335724-16335725	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs569704825	chr4:16335739-16335740	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs569552084	chr4:16335748-16335749	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs556548298	chr4:16335765-16335766	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs548506100	chr4:16335793-16335794	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs568018367	chr4:16335798-16335799	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs537067419	chr4:16335882-16335883	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs550625768	chr4:16335894-16335895	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs570438862	chr4:16336007-16336008	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs2041538	chr4:16336013-16336014	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
22	rs143931604	chr4:16336037-16336038	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs566269648	chr4:16336075-16336076	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs534947429	chr4:16336082-16336083	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs554860623	chr4:16336212-16336213	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs574462057	chr4:16336277-16336278	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs148647896	chr4:16336303-16336304	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs181313793	chr4:16336341-16336342	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs73798737	chr4:16336347-16336348	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs546324467	chr4:16336396-16336397	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs559234386	chr4:16336411-16336412	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs185135223	chr4:16336412-16336413	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs542117888	chr4:16336420-16336421	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs73239725	chr4:16336444-16336445	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs530861009	chr4:16336459-16336460	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs550297787	chr4:16336500-16336501	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs191122581	chr4:16336609-16336610	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs571393456	chr4:16336628-16336629	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs532844220	chr4:16336640-16336641	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs546686071	chr4:16336655-16336656	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs565903213	chr4:16336665-16336666	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs534907993	chr4:16336691-16336692	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs146680329	chr4:16336715-16336716	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs140237375	chr4:16336719-16336720	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs568395638	chr4:16336739-16336740	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs111965123	chr4:16336750-16336751	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs113249567	chr4:16336759-16336760	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs143861640	chr4:16336804-16336805	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs73127519	chr4:16336847-16336848	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs577172676	chr4:16336855-16336856	Weak transcription Enhancers	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:58 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:16331600-16336000	Weak transcription	Fetal Kidney	kidney
2	chr4:16335400-16338400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
3	chr4:16336000-16337200	Enhancers	Fetal Kidney	kidney
4	chr4:16338400-16338600	ZNF genes & repeats	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
5	chr4:16338600-16353200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
6	chr4:16339800-16340200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
7	chr4:16339800-16340200	Enhancers	NH-A	brain
8	chr4:16339800-16340200	Enhancers	NHEK	skin
9	chr4:16339800-16341000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
10	chr4:16349800-16350000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
11	chr4:16350000-16352800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
12	chr4:16350200-16350600	Enhancers	Spleen	Spleen
13	chr4:16351400-16351600	Enhancers	iPS-20b Cell Line	embryonic stem cell
14	chr4:16351400-16354000	Enhancers	HUES64 Cell Line	embryonic stem cell
15	chr4:16351600-16351800	Enhancers	HUES48 Cell Line	embryonic stem cell
16	chr4:16351600-16351800	Enhancers	HUES6 Cell Line	embryonic stem cell
17	chr4:16351600-16351800	Enhancers	iPS-18 Cell Line	embryonic stem cell
18	chr4:16351600-16352200	Enhancers	iPS-15b Cell Line	embryonic stem cell
19	chr4:16351600-16352200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
20	chr4:16351800-16352800	Weak transcription	HUES48 Cell Line	embryonic stem cell
21	chr4:16351800-16353000	Weak transcription	HUES6 Cell Line	embryonic stem cell
22	chr4:16352000-16353000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
23	chr4:16352200-16352600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
24	chr4:16352200-16353000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
25	chr4:16352200-16353200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
26	chr4:16352200-16353800	Enhancers	Brain Germinal Matrix	brain
27	chr4:16352600-16355000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
28	chr4:16352800-16353800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
29	chr4:16352800-16353800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
30	chr4:16352800-16353800	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
31	chr4:16352800-16353800	Enhancers	HUES48 Cell Line	embryonic stem cell
32	chr4:16352800-16353800	Enhancers	Fetal Brain Female	brain
33	chr4:16353000-16353600	Enhancers	iPS-18 Cell Line	embryonic stem cell
34	chr4:16353000-16353800	Enhancers	HUES6 Cell Line	embryonic stem cell
35	chr4:16353000-16353800	Enhancers	iPS-20b Cell Line	embryonic stem cell
36	chr4:16353000-16353800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
37	chr4:16353000-16353800	Enhancers	Cortex derived primary cultured neurospheres	brain
38	chr4:16353000-16353800	Enhancers	Brain Cingulate Gyrus	brain
39	chr4:16353200-16353400	Enhancers	iPS-15b Cell Line	embryonic stem cell
40	chr4:16353200-16353800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
41	chr4:16353200-16353800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
42	chr4:16353200-16353800	Enhancers	Brain Substantia Nigra	brain
43	chr4:16353400-16353800	Enhancers	Brain Hippocampus Middle	brain
44	chr4:16353800-16354600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
45	chr4:16353800-16355000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
46	chr4:16354800-16355000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
47	chr4:16355000-16355200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
48	chr4:16357200-16358400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
49	chr4:16359200-16359600	Enhancers	Fetal Stomach	stomach
50	chr4:16362200-16362600	Active TSS	K562	blood

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