Variant report

Variant	nsv593779
Chromosome Location	chr4:16336013-16375164
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:12)
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	chr4:16339574-16339817	MCF10A-Er-Src	breast:	n/a	n/a
4	E2F4	chr4:16366375-16366575	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	chr4:16339477-16339919	MCF10A-Er-Src	breast:	n/a	chr4:16339607-16339615 chr4:16339605-16339617 chr4:16339607-16339615 chr4:16339608-16339615
13	FOS	chr4:16339479-16339925	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	chr4:16339529-16339883	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	chr4:16367690-16367765	HepG2	liver:	n/a	n/a
20	MAFK	chr4:16348552-16348793	HepG2	liver:	n/a	n/a
21	MAFK	chr4:16346479-16346552	HepG2	liver:	n/a	n/a
22	MAFK	chr4:16348561-16348761	HepG2	liver:	n/a	n/a
23	MAX	chr4:16362167-16362522	K562	blood:	n/a	n/a
24	MAX	chr4:16362445-16362769	MCF-7	breast:	n/a	n/a
25	MAX	chr4:16354947-16355115	NB4	blood:	n/a	chr4:16354987-16354997
26	MYC	chr4:16362408-16362824	MCF-7	breast:	n/a	n/a
27	MYC	chr4:16362417-16362669	MCF-7	breast:	n/a	n/a
28	MYC	chr4:16362427-16362723	MCF-7	breast:	n/a	n/a
29	MYC	chr4:16362429-16362626	H1-hESC	embryonic stem cell:	n/a	n/a
30	MYC	chr4:16339630-16339719	MCF10A-Er-Src	breast:	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	chr4:16362130-16363282	MCF-7	breast:	n/a	n/a
34	POLR2A	chr4:16353183-16353327	MCF10A-Er-Src	breast:	n/a	n/a
35	POLR2A	chr4:16362334-16362650	K562	blood:	n/a	n/a
36	POLR2A	chr4:16338940-16338946	MCF10A-Er-Src	breast:	n/a	n/a
37	POLR2A	chr4:16368672-16368763	MCF10A-Er-Src	breast:	n/a	n/a
38	POLR2A	chr4:16362508-16362535	ProgFib	skin:	n/a	n/a
39	POLR2A	chr4:16338261-16338296	MCF10A-Er-Src	breast:	n/a	n/a
40	POLR2A	chr4:16359970-16360061	K562	blood:	n/a	n/a
41	POLR2A	chr4:16336236-16336684	SK-N-MC	brain:	n/a	n/a
42	POLR2A	chr4:16362267-16362328	K562	blood:	n/a	n/a
43	POLR2A	chr4:16362561-16362776	ProgFib	skin:	n/a	n/a
44	POLR2A	chr4:16365781-16365862	MCF10A-Er-Src	breast:	n/a	n/a
45	POLR2A	chr4:16362107-16362125	MCF-7	breast:	n/a	n/a
46	POLR2A	chr4:16354902-16355014	ProgFib	skin:	n/a	n/a
47	POLR2A	chr4:16366829-16367151	H1-neurons	neurons:	n/a	n/a
48	POLR2A	chr4:16362271-16362913	MCF-7	breast:	n/a	n/a
49	POLR2A	chr4:16362252-16362898	MCF-7	breast:	n/a	n/a
50	POLR2A	chr4:16344102-16344244	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	chr4:16359846-16359896	NHDF-neo	bronchial:	n/a
2	chr4:16362664-16362714	Hepatocyte	liver:	n/a
3	chr4:16362666-16362716	HCPEpiC	choroid plexus:	n/a
4	chr4:16362666-16362716	GM12891	blood:	n/a
5	chr4:16362422-16362472	RPTEC	kidney:	n/a
6	chr4:16362422-16362472	HPAEpiC	pulmonary alveolar:	n/a
7	chr4:16362664-16362714	HEK293	kidney:	embryo
8	chr4:16363266-16363316	H1-hESC	embryonic stem cell:	embryo
9	chr4:16362584-16362634	SK-N-SH	brain:	n/a
10	chr4:16362664-16362714	IMR90	lung:	fetal
11	chr4:16362340-16362390	NHBE	bronchial:	n/a
12	chr4:16363266-16363316	ovcar-3	ovarian:	n/a
13	chr4:16362666-16362716	AG04450	lung:	fetal
14	chr4:16363266-16363316	SAEC	small airway:	n/a
15	chr4:16363266-16363316	HRCEpiC	kidney:	n/a
16	chr4:16362664-16362714	HL-60	blood:	n/a
17	chr4:16359846-16359896	MCF-7	breast:	n/a
18	chr4:16362664-16362714	GM12891	blood:	n/a
19	chr4:16362340-16362390	Caco-2	colon:	n/a
20	chr4:16363266-16363316	AG09309	skin:	n/a
21	chr4:16362584-16362634	HAEpiC	amniotic membrane:	n/a
22	chr4:16362666-16362716	PFSK-1	brain:	n/a
23	chr4:16362584-16362634	GM12878	blood:	n/a
24	chr4:16362340-16362390	H1-hESC	embryonic stem cell:	embryo
25	chr4:16359846-16359896	CMK	blood:	n/a
26	chr4:16366593-16366643	ProgFib	skin:	n/a
27	chr4:16362666-16362716	H1-hESC	embryonic stem cell:	embryo
28	chr4:16359846-16359896	H1-hESC	embryonic stem cell:	embryo
29	chr4:16363266-16363316	SKMC	muscle:	n/a
30	chr4:16359846-16359896	NB4	blood:	n/a
31	chr4:16362584-16362634	NHDF-neo	bronchial:	n/a
32	chr4:16359846-16359896	HL-60	blood:	n/a
33	chr4:16362422-16362472	AG09319	gingival:	n/a
34	chr4:16362340-16362390	GM19239	blood:	n/a
35	chr4:16362584-16362634	PrEC	prostate:	n/a
36	chr4:16362666-16362716	NH-A	brain:	n/a
37	chr4:16363266-16363316	T-47D	breast:	n/a
38	chr4:16362666-16362716	PrEC	prostate:	n/a
39	chr4:16362664-16362714	A549	lung:	n/a
40	chr4:16366593-16366643	LNCaP	prostate:	n/a
41	chr4:16366593-16366643	HPAEpiC	pulmonary alveolar:	n/a
42	chr4:16359846-16359896	AG09309	skin:	n/a
43	chr4:16359846-16359896	GM19239	blood:	n/a
44	chr4:16362666-16362716	ProgFib	skin:	n/a
45	chr4:16363266-16363316	GM06990	blood:	n/a
46	chr4:16363266-16363316	HPAEpiC	pulmonary alveolar:	n/a
47	chr4:16359846-16359896	MCF10A-Er-Src	breast:	n/a
48	chr4:16362422-16362472	BJ	skin:	n/a
49	chr4:16362666-16362716	HCT-116	colon:	n/a
50	chr4:16359846-16359896	HRPEpiC	eye:	n/a

(count:12 , 50 per page) page: 1

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

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CD38-2	chr4:16357243-16357365	XLOC_003469
2	lnc-TAPT1-3	chr4:16362507-16362611	NONHSAT095687
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: 970 )
Associated
traits (count: 51 )

Variant overlapped rSNPs/rCNVs (count:970 , 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	rs2041538	chr4:16336013-16336014	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs143931604	chr4:16336037-16336038	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs566269648	chr4:16336075-16336076	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs534947429	chr4:16336082-16336083	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs554860623	chr4:16336212-16336213	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs574462057	chr4:16336277-16336278	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs148647896	chr4:16336303-16336304	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs181313793	chr4:16336341-16336342	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs73798737	chr4:16336347-16336348	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs546324467	chr4:16336396-16336397	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs559234386	chr4:16336411-16336412	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs185135223	chr4:16336412-16336413	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs542117888	chr4:16336420-16336421	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs73239725	chr4:16336444-16336445	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs530861009	chr4:16336459-16336460	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs550297787	chr4:16336500-16336501	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs191122581	chr4:16336609-16336610	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs571393456	chr4:16336628-16336629	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs532844220	chr4:16336640-16336641	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs546686071	chr4:16336655-16336656	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs565903213	chr4:16336665-16336666	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs534907993	chr4:16336691-16336692	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs146680329	chr4:16336715-16336716	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs140237375	chr4:16336719-16336720	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs568395638	chr4:16336739-16336740	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs111965123	chr4:16336750-16336751	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs113249567	chr4:16336759-16336760	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs143861640	chr4:16336804-16336805	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs73127519	chr4:16336847-16336848	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs577172676	chr4:16336855-16336856	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs375940334	chr4:16336856-16336857	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs151330394	chr4:16336879-16336880	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs532320405	chr4:16336941-16336942	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs372776533	chr4:16336964-16336965	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs140536471	chr4:16337029-16337030	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs78274335	chr4:16337031-16337032	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs183711254	chr4:16337035-16337036	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs561906234	chr4:16337060-16337061	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs150463667	chr4:16337071-16337072	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs78234456	chr4:16337100-16337101	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs73127521	chr4:16337102-16337103	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs532961662	chr4:16337135-16337136	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs544579480	chr4:16337214-16337215	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs370642892	chr4:16337227-16337228	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs546352573	chr4:16337252-16337253	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs566206217	chr4:16337262-16337263	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs75252501	chr4:16337280-16337281	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs117729602	chr4:16337290-16337291	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs188995857	chr4:16337309-16337310	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs115995358	chr4:16337334-16337335	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:57 , 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	chr4:16336000-16337200	Enhancers	Fetal Kidney	kidney
3	chr4:16338400-16338600	ZNF genes & repeats	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
4	chr4:16338600-16353200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
5	chr4:16339800-16340200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
6	chr4:16339800-16340200	Enhancers	NH-A	brain
7	chr4:16339800-16340200	Enhancers	NHEK	skin
8	chr4:16339800-16341000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
9	chr4:16349800-16350000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
10	chr4:16350000-16352800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
11	chr4:16350200-16350600	Enhancers	Spleen	Spleen
12	chr4:16351400-16351600	Enhancers	iPS-20b Cell Line	embryonic stem cell
13	chr4:16351400-16354000	Enhancers	HUES64 Cell Line	embryonic stem cell
14	chr4:16351600-16351800	Enhancers	HUES48 Cell Line	embryonic stem cell
15	chr4:16351600-16351800	Enhancers	HUES6 Cell Line	embryonic stem cell
16	chr4:16351600-16351800	Enhancers	iPS-18 Cell Line	embryonic stem cell
17	chr4:16351600-16352200	Enhancers	iPS-15b Cell Line	embryonic stem cell
18	chr4:16351600-16352200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
19	chr4:16351800-16352800	Weak transcription	HUES48 Cell Line	embryonic stem cell
20	chr4:16351800-16353000	Weak transcription	HUES6 Cell Line	embryonic stem cell
21	chr4:16352000-16353000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
22	chr4:16352200-16352600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
23	chr4:16352200-16353000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
24	chr4:16352200-16353200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
25	chr4:16352200-16353800	Enhancers	Brain Germinal Matrix	brain
26	chr4:16352600-16355000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
27	chr4:16352800-16353800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
28	chr4:16352800-16353800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
29	chr4:16352800-16353800	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
30	chr4:16352800-16353800	Enhancers	HUES48 Cell Line	embryonic stem cell
31	chr4:16352800-16353800	Enhancers	Fetal Brain Female	brain
32	chr4:16353000-16353600	Enhancers	iPS-18 Cell Line	embryonic stem cell
33	chr4:16353000-16353800	Enhancers	HUES6 Cell Line	embryonic stem cell
34	chr4:16353000-16353800	Enhancers	iPS-20b Cell Line	embryonic stem cell
35	chr4:16353000-16353800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
36	chr4:16353000-16353800	Enhancers	Cortex derived primary cultured neurospheres	brain
37	chr4:16353000-16353800	Enhancers	Brain Cingulate Gyrus	brain
38	chr4:16353200-16353400	Enhancers	iPS-15b Cell Line	embryonic stem cell
39	chr4:16353200-16353800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
40	chr4:16353200-16353800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
41	chr4:16353200-16353800	Enhancers	Brain Substantia Nigra	brain
42	chr4:16353400-16353800	Enhancers	Brain Hippocampus Middle	brain
43	chr4:16353800-16354600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
44	chr4:16353800-16355000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
45	chr4:16354800-16355000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
46	chr4:16355000-16355200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
47	chr4:16357200-16358400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
48	chr4:16359200-16359600	Enhancers	Fetal Stomach	stomach
49	chr4:16362200-16362600	Active TSS	K562	blood
50	chr4:16362400-16363000	Active TSS	Placenta	Placenta

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