Variant report

Variant	nsv593207
Chromosome Location	chr4:629437-645300
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:80)
CpG islands
(count:795)
Chromatin interactive
region (count:21)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:80 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF3	chr4:631450-631647	K562	blood:	n/a	n/a
2	BHLHE40	chr4:641442-641466	HepG2	liver:	n/a	n/a
3	BHLHE40	chr4:631420-631748	K562	blood:	n/a	n/a
4	CBX3	chr4:640330-640691	K562	blood:	n/a	n/a
5	CTCF	chr4:643180-643330	WERI-Rb-1	eye:	n/a	chr4:643281-643294
6	CTCF	chr4:640260-640410	BE2_C	brain:	n/a	n/a
7	CTCF	chr4:640300-640450	HVMF	connective:	n/a	n/a
8	CTCF	chr4:640460-640610	K562	blood:	n/a	n/a
9	CTCF	chr4:642883-643005	K562	blood:	n/a	n/a
10	CTCF	chr4:640372-640639	K562	blood:	n/a	n/a
11	CTCF	chr4:640373-640604	K562	blood:	n/a	n/a
12	CTCF	chr4:640440-640590	BE2_C	brain:	n/a	n/a
13	CTCF	chr4:640320-640470	HMEC	breast:	n/a	n/a
14	CTCF	chr4:642340-642490	WERI-Rb-1	eye:	n/a	chr4:642369-642382 chr4:642376-642389
15	CTCF	chr4:642907-642979	K562	blood:	n/a	n/a
16	CTCF	chr4:640424-640550	Spleen_OC	spleen:	n/a	n/a
17	CTCF	chr4:640380-640530	HMF	breast:	n/a	n/a
18	CTCF	chr4:642820-642970	WERI-Rb-1	eye:	n/a	n/a
19	CTCF	chr4:640426-640588	K562	blood:	n/a	n/a
20	CTCF	chr4:640358-640586	K562	blood:	n/a	n/a
21	CTCF	chr4:642840-642990	WERI-Rb-1	eye:	n/a	n/a
22	CTCF	chr4:640460-640610	HMEC	breast:	n/a	n/a
23	CTCFL	chr4:640392-640616	K562	blood:	n/a	n/a
24	CTCFL	chr4:640371-640569	K562	blood:	n/a	n/a
25	E2F4	chr4:640167-640261	MCF10A-Er-Src	breast:	n/a	n/a
26	E2F6	chr4:631471-631569	K562	blood:	n/a	n/a
27	E2F6	chr4:642137-642282	K562	blood:	n/a	n/a
28	E2F6	chr4:640298-640599	K562	blood:	n/a	n/a
29	EGR1	chr4:640257-640599	K562	blood:	n/a	n/a
30	EGR1	chr4:640196-640554	K562	blood:	n/a	n/a
31	ELF1	chr4:640316-640598	K562	blood:	n/a	chr4:640522-640535 chr4:640524-640535 chr4:640495-640504
32	ELF1	chr4:640301-640720	K562	blood:	n/a	chr4:640522-640535 chr4:640524-640535 chr4:640495-640504
33	FOXA1	chr4:644781-645158	HepG2	liver:	n/a	n/a
34	FOXA1	chr4:644686-645187	HepG2	liver:	n/a	n/a
35	FOXA1	chr4:644734-644994	HepG2	liver:	n/a	n/a
36	FOXA2	chr4:644822-645107	HepG2	liver:	n/a	n/a
37	GABPA	chr4:645281-645660	H1-hESC	embryonic stem cell:	n/a	n/a
38	GABPA	chr4:640245-640710	K562	blood:	n/a	n/a
39	HCFC1	chr4:640322-640646	K562	blood:	n/a	n/a
40	HEY1	chr4:640430-640633	K562	blood:	n/a	n/a
41	HMGN3	chr4:640393-640530	K562	blood:	n/a	n/a
42	HMGN3	chr4:642557-642694	K562	blood:	n/a	n/a
43	IRF1	chr4:641935-642218	K562	blood:	n/a	chr4:642054-642071 chr4:642057-642069
44	JUND	chr4:640394-640658	K562	blood:	n/a	n/a
45	JUND	chr4:635924-636353	HepG2	liver:	n/a	n/a
46	MAX	chr4:641999-642094	HepG2	liver:	n/a	chr4:642029-642038 chr4:642027-642040 chr4:642029-642036 chr4:642027-642040
47	MAX	chr4:641941-642096	K562	blood:	n/a	chr4:642029-642038 chr4:642027-642040 chr4:642029-642036 chr4:642027-642040
48	MAX	chr4:641844-642214	K562	blood:	n/a	chr4:642029-642038 chr4:642027-642040 chr4:642029-642036 chr4:642027-642040
49	MAX	chr4:642452-642833	K562	blood:	n/a	n/a
50	MAX	chr4:640377-640585	K562	blood:	n/a	chr4:640462-640472

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:644805-644855	NT2-D1	testis:	n/a
2	chr4:642765-642815	A549	lung:	n/a
3	chr4:644805-644855	NT2-D1	testis:	n/a
4	chr4:642765-642815	A549	lung:	n/a
5	chr4:644572-644622	ECC-1	luminal epithelium:	n/a
6	chr4:644973-645023	CMK	blood:	n/a
7	chr4:631579-631629	HCM	heart:	n/a
8	chr4:642765-642815	LNCaP	prostate:	n/a
9	chr4:631579-631629	SKMC	muscle:	n/a
10	chr4:642885-642935	NHDF-neo	bronchial:	n/a
11	chr4:631579-631629	AG09319	gingival:	n/a
12	chr4:642765-642815	AG10803	skin:	n/a
13	chr4:644973-645023	LNCaP	prostate:	n/a
14	chr4:645256-645306	AG09309	skin:	n/a
15	chr4:640503-640553	HRE	kidney:	n/a
16	chr4:642885-642935	PANC-1	pancreas:	n/a
17	chr4:631734-631784	PFSK-1	brain:	n/a
18	chr4:640503-640553	K562	blood:	n/a
19	chr4:640594-640644	NH-A	brain:	n/a
20	chr4:645256-645306	CMK	blood:	n/a
21	chr4:640503-640553	H1-hESC	embryonic stem cell:	embryo
22	chr4:629434-629484	Hepatocyte	liver:	n/a
23	chr4:629434-629484	U87	brain:	n/a
24	chr4:640594-640644	HIPEpiC	eye:	n/a
25	chr4:642885-642935	LNCaP	prostate:	n/a
26	chr4:644572-644622	HEK293	kidney:	embryo
27	chr4:644805-644855	Jurkat	blood:	n/a
28	chr4:640348-640398	GM06990	blood:	n/a
29	chr4:642885-642935	HRE	kidney:	n/a
30	chr4:631579-631629	HUVEC	blood vessel:	n/a
31	chr4:645256-645306	HPAEpiC	pulmonary alveolar:	n/a
32	chr4:629434-629484	K562	blood:	n/a
33	chr4:640348-640398	HEK293	kidney:	embryo
34	chr4:645256-645306	PFSK-1	brain:	n/a
35	chr4:642765-642815	ProgFib	skin:	n/a
36	chr4:645256-645306	BJ	skin:	n/a
37	chr4:629434-629484	HL-60	blood:	n/a
38	chr4:631734-631784	HCPEpiC	choroid plexus:	n/a
39	chr4:640348-640398	NHDF-neo	bronchial:	n/a
40	chr4:640348-640398	HEEpiC	esophagus:	n/a
41	chr4:642691-642741	PrEC	prostate:	n/a
42	chr4:640348-640398	AG09309	skin:	n/a
43	chr4:640594-640644	GM06990	blood:	n/a
44	chr4:642691-642741	H1-hESC	embryonic stem cell:	embryo
45	chr4:645256-645306	PrEC	prostate:	n/a
46	chr4:644973-645023	HMEC	breast:	n/a
47	chr4:644572-644622	MCF10A-Er-Src	breast:	n/a
48	chr4:644572-644622	ProgFib	skin:	n/a
49	chr4:631734-631784	ECC-1	luminal epithelium:	n/a
50	chr4:642691-642741	K562	blood:	n/a

(count:21 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:615876..617771-chr4:628086..630978,3	K562	blood:
2	chr4:623895..625703-chr4:641254..643295,2	K562	blood:
3	chr4:642830..644425-chr4:665822..667972,2	K562	blood:
4	chr4:636743..639513-chr4:642400..644519,2	MCF-7	breast:
5	chr4:642166..643700-chr4:648904..650417,2	MCF-7	breast:
6	chr4:640175..641727-chr4:663332..665885,2	K562	blood:
7	chr4:640899..644048-chr4:645918..649470,4	K562	blood:
8	chr4:629516..632051-chr4:640070..643057,2	MCF-7	breast:
9	chr4:644054..646414-chr4:656838..659721,2	MCF-7	breast:
10	chr4:642255..644273-chr4:662905..665187,2	K562	blood:
11	chr4:642131..644821-chr4:649750..652284,2	MCF-7	breast:
12	chr4:636743..639513-chr4:642400..644519,2	MCF-7	breast:
13	chr4:629506..631102-chr4:666468..668539,2	K562	blood:
14	chr4:636643..638712-chr4:668092..669702,2	MCF-7	breast:
15	chr4:644808..646339-chr4:648173..650037,2	K562	blood:
16	chr4:629516..632051-chr4:640070..643057,2	MCF-7	breast:
17	chr4:514493..516331-chr4:631156..634018,2	K562	blood:
18	chr4:642559..644121-chr4:666907..669790,2	MCF-7	breast:
19	chr4:641525..644066-chr4:652058..654958,2	K562	blood:
20	chr4:626527..629135-chr4:629423..631548,2	MCF-7	breast:
21	chr4:644162..647846-chr4:649268..652076,4	MCF-7	breast:

No data

Variant related genes	Relation type
PDE6B	TF binding region
PDE6B	CpG island
ENSG00000174227	chromatin interactions
ENSG00000215375	chromatin interactions
ENSG00000169020	chromatin interactions
ENSG00000242686	chromatin interactions
ENSG00000133256	chromatin interactions

Extended variants
information (count: 721 )
Associated
traits (count: 68 )

Variant overlapped rSNPs/rCNVs (count:721 , 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	rs28538930	chr4:629437-629438	Weak transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs188885070	chr4:629481-629482	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
3	rs181634311	chr4:629482-629483	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
4	rs544289909	chr4:629483-629484	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
5	rs78918869	chr4:629493-629494	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
6	rs557220234	chr4:629548-629549	Weak transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs575477559	chr4:629576-629577	Weak transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs185260449	chr4:629582-629583	Weak transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs542519695	chr4:629583-629584	Weak transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs561255665	chr4:629595-629596	Weak transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs572857110	chr4:629609-629610	Weak transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs73056580	chr4:629610-629611	Weak transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs189710914	chr4:629616-629617	Weak transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs564637157	chr4:629644-629645	Weak transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs532105875	chr4:629645-629646	Weak transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs375116150	chr4:629680-629681	Weak transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs551545798	chr4:629681-629682	Weak transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs200664252	chr4:629698-629699	Weak transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs62295357	chr4:629702-629703	Weak transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs199674705	chr4:629710-629711	Weak transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs201584824	chr4:629729-629730	Weak transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs201593198	chr4:629741-629742	Weak transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs148264146	chr4:629746-629747	Weak transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs374915809	chr4:629747-629748	Weak transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs369318359	chr4:629748-629749	Weak transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs554692149	chr4:629749-629750	Weak transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs75543439	chr4:629753-629754	Weak transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs201100689	chr4:629768-629769	Weak transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs111340191	chr4:629769-629770	Weak transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs369780942	chr4:629790-629791	Weak transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs200202473	chr4:629792-629793	Weak transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs373926401	chr4:629808-629809	Weak transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs554561473	chr4:629816-629817	Weak transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs111666091	chr4:629829-629830	Weak transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs372750545	chr4:629891-629892	Weak transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs558166590	chr4:629941-629942	Weak transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs544329710	chr4:629960-629961	Weak transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs62295358	chr4:629992-629993	Weak transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs141270814	chr4:630038-630039	Weak transcription ZNF genes & repeats Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs562606802	chr4:630046-630047	Weak transcription ZNF genes & repeats Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs530971866	chr4:630079-630080	Weak transcription ZNF genes & repeats Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs375444694	chr4:630081-630082	Weak transcription ZNF genes & repeats Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs561419782	chr4:630101-630102	Weak transcription ZNF genes & repeats Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs528820745	chr4:630104-630105	Weak transcription ZNF genes & repeats Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs546999769	chr4:630148-630149	Weak transcription ZNF genes & repeats Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs571632922	chr4:630162-630163	Weak transcription ZNF genes & repeats Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs368803187	chr4:630180-630181	Weak transcription ZNF genes & repeats Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs550748556	chr4:630188-630189	Weak transcription ZNF genes & repeats Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs34953355	chr4:630192-630193	Weak transcription ZNF genes & repeats Bivalent Enhancer	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
50	rs112120206	chr4:630198-630199	Weak transcription ZNF genes & repeats Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:68)

Disease	PMID	Source
Myelofibrosis	22110671	CNVD
Wolf-Hirschhorn syndrome	21549014	CNVD
Breast cancer	21806811	CNVD
Wolf-Hirschhorn syndrome	22283845	CNVD
Wolf-Hirschhorn syndrome	16773131	CNVD
Mental retardation	16773131	CNVD
Wolf-Hirschhorn syndrome	22470819	CNVD
Wolf-Hirschhorn syndrome	18541967	CNVD
sporadic birth defects	19047251	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Retinitis pigmentosa	18421352	CNVD
Wolf-Hirschhorn syndrome	19259404	CNVD
Bladder cancer	19242612	CNVD
Breast cancer	19242612	CNVD
Congenital anomalies of the kidney and urinary tract	19242612	CNVD
abnormal development	18461090	CNVD
Olfactory neuroblastoma	18408657	CNVD
Wilms tumour	21544195	CNVD
Melanoma	20688739	CNVD
Colorectal cancer	16272173	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	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
small cell lung cancer	20016488	CNVD
Breast cancer	17142309	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Developmental delay	21147756	CNVD
Urothelial carcinoma	21177765	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Lung cancer	18438408	CNVD
Prostate cancer	18632612	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Pancreatic cancer	17952125	CNVD
Type 2 diabetes	21754918	CNVD
Breast cancer	22522925	CNVD
Breast cancer	21509527	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:138 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:624600-630400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
2	chr4:626400-642000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
3	chr4:626800-630400	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin01	Skin
4	chr4:627000-633000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
5	chr4:629400-630400	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
6	chr4:630000-631600	Bivalent Enhancer	Fetal Muscle Trunk	muscle
7	chr4:630200-630400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
8	chr4:630200-631000	Bivalent Enhancer	Fetal Stomach	stomach
9	chr4:630400-630600	Strong transcription	iPS DF 19.11 Cell Line	embryonic stem cell
10	chr4:630400-632000	Enhancers	Fetal Brain Male	brain
11	chr4:630600-630800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
12	chr4:630600-631400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
13	chr4:630600-631800	Bivalent Enhancer	Fetal Muscle Leg	muscle
14	chr4:630800-632000	Enhancers	Fetal Kidney	kidney
15	chr4:631400-631600	Bivalent Enhancer	Placenta	Placenta
16	chr4:631400-631800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
17	chr4:631400-631800	Active TSS	Brain Hippocampus Middle	brain
18	chr4:631400-631800	Enhancers	Brain Inferior Temporal Lobe	brain
19	chr4:631400-632000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
20	chr4:631400-632000	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin03	Skin
21	chr4:631400-632000	Active TSS	Fetal Brain Female	brain
22	chr4:631400-657000	Weak transcription	Right Atrium	heart
23	chr4:631800-632000	Enhancers	Brain Substantia Nigra	brain
24	chr4:640000-640200	Enhancers	Placenta	Placenta
25	chr4:640000-640400	Active TSS	Primary T cells from cord blood	blood
26	chr4:640000-640400	Active TSS	Primary T helper naive cells fromperipheralblood	blood
27	chr4:640000-640400	Active TSS	Primary T regulatory cells fromperipheralblood	blood
28	chr4:640000-640600	Active TSS	Primary T killer memory cells from peripheral blood	blood
29	chr4:640000-640600	Active TSS	HMEC	breast
30	chr4:640000-640800	Bivalent/Poised TSS	Brain Germinal Matrix	brain
31	chr4:640200-640400	Flanking Bivalent TSS/Enh	Primary hematopoietic stem cells	blood
32	chr4:640200-640400	Flanking Active TSS	Placenta	Placenta
33	chr4:640200-640600	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
34	chr4:640200-640600	Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
35	chr4:640200-640600	Bivalent Enhancer	Fetal Muscle Trunk	muscle
36	chr4:640200-640800	Flanking Bivalent TSS/Enh	Fetal Muscle Leg	muscle
37	chr4:640400-640600	Enhancers	Gastric	stomach
38	chr4:640400-643800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
39	chr4:640400-648400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
40	chr4:640600-642600	Weak transcription	Gastric	stomach
41	chr4:640800-642200	Bivalent Enhancer	Fetal Muscle Leg	muscle
42	chr4:641400-641600	Enhancers	ES-WA7 Cell Line	embryonic stem cell
43	chr4:641600-642200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
44	chr4:641800-642000	Enhancers	HepG2	liver
45	chr4:641800-642200	Enhancers	iPS-15b Cell Line	embryonic stem cell
46	chr4:641800-642800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
47	chr4:641800-657000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
48	chr4:642000-642200	Flanking Bivalent TSS/Enh	HepG2	liver
49	chr4:642000-642600	Enhancers	ES-I3 Cell Line	embryonic stem cell
50	chr4:642000-642600	Bivalent Enhancer	Fetal Muscle Trunk	muscle

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