Variant report

Variant	nsv461193
Chromosome Location	chr4:7154743-7197393
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1202)
CpG islands
(count:1405)
Chromatin interactive
region (count:32)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1202 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:7187928-7188138	HepG2	liver:	n/a	n/a
2	BACH1	chr4:7194041-7194352	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr4:7194892-7195086	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr4:7195510-7195602	H1-hESC	embryonic stem cell:	n/a	n/a
5	BHLHE40	chr4:7158174-7158813	K562	blood:	n/a	n/a
6	BHLHE40	chr4:7157510-7157791	K562	blood:	n/a	n/a
7	BHLHE40	chr4:7169218-7169548	HepG2	liver:	n/a	n/a
8	CCNT2	chr4:7194155-7194325	K562	blood:	n/a	n/a
9	CEBPB	chr4:7166209-7166391	A549	lung:	n/a	n/a
10	CEBPB	chr4:7166191-7166447	HepG2	liver:	n/a	n/a
11	CEBPB	chr4:7186098-7186251	HepG2	liver:	n/a	n/a
12	CEBPZ	chr4:7172080-7172092	HepG2	liver:	n/a	n/a
13	CHD1	chr4:7193915-7194518	IMR90	lung:	n/a	n/a
14	CHD2	chr4:7193989-7194327	Hela-S3	cervix:	n/a	n/a
15	CREB1	chr4:7194040-7194391	A549	lung:	n/a	n/a
16	CREB1	chr4:7187886-7188118	A549	lung:	n/a	n/a
17	CTBP2	chr4:7194058-7194389	H1-hESC	embryonic stem cell:	n/a	n/a
18	CTCF	chr4:7189102-7189179	HepG2	liver:	n/a	chr4:7189128-7189141
19	CTCF	chr4:7194060-7194210	GM12875	blood:	n/a	n/a
20	CTCF	chr4:7187884-7188122	GM19238	blood:	n/a	chr4:7187933-7187946 chr4:7187937-7187946
21	CTCF	chr4:7187940-7188090	GM12873	blood:	n/a	n/a
22	CTCF	chr4:7191435-7191932	MCF-7	breast:	n/a	n/a
23	CTCF	chr4:7163580-7163730	AoAF	blood vessel:	n/a	n/a
24	CTCF	chr4:7194060-7194210	WI-38	lung:	n/a	n/a
25	CTCF	chr4:7158660-7158810	GM12868	blood:	n/a	n/a
26	CTCF	chr4:7158680-7158830	HMEC	breast:	n/a	n/a
27	CTCF	chr4:7196300-7196450	HA-sp	spinal cord:	n/a	chr4:7196329-7196342 chr4:7196327-7196343 chr4:7196326-7196344 chr4:7196328-7196349 chr4:7196329-7196338
28	CTCF	chr4:7158680-7158830	HPAF	blood vessel:	n/a	n/a
29	CTCF	chr4:7191645-7191754	Kidney_OC	kidney:	n/a	n/a
30	CTCF	chr4:7188984-7189227	K562	blood:	n/a	chr4:7189128-7189141 chr4:7189035-7189043
31	CTCF	chr4:7191664-7191762	GM12878	blood:	n/a	n/a
32	CTCF	chr4:7193976-7194360	K562	blood:	n/a	n/a
33	CTCF	chr4:7194035-7194330	GM12891	blood:	n/a	n/a
34	CTCF	chr4:7156080-7156230	GM12867	blood:	n/a	n/a
35	CTCF	chr4:7187891-7188089	MCF-7	breast:	n/a	chr4:7187933-7187946 chr4:7187937-7187946
36	CTCF	chr4:7158240-7158390	GM12872	blood:	n/a	n/a
37	CTCF	chr4:7187900-7188050	AoAF	blood vessel:	n/a	chr4:7187933-7187946 chr4:7187937-7187946
38	CTCF	chr4:7194057-7194332	Medullo	brain:	n/a	n/a
39	CTCF	chr4:7157180-7157330	HepG2	liver:	n/a	n/a
40	CTCF	chr4:7158672-7158863	HUVEC	blood vessel:	n/a	n/a
41	CTCF	chr4:7187900-7188050	WERI-Rb-1	eye:	n/a	chr4:7187933-7187946 chr4:7187937-7187946
42	CTCF	chr4:7196240-7196530	A549	lung:	n/a	chr4:7196329-7196342 chr4:7196327-7196343 chr4:7196326-7196344 chr4:7196328-7196349 chr4:7196329-7196338
43	CTCF	chr4:7194025-7194314	GM12892	blood:	n/a	n/a
44	CTCF	chr4:7187920-7188070	A549	lung:	n/a	chr4:7187933-7187946 chr4:7187937-7187946
45	CTCF	chr4:7195637-7195680	Hela-S3	cervix:	n/a	n/a
46	CTCF	chr4:7194080-7194230	HCM	heart:	n/a	n/a
47	CTCF	chr4:7169545-7169745	K562	blood:	n/a	chr4:7169658-7169679 chr4:7169606-7169619 chr4:7169664-7169680 chr4:7169663-7169681
48	CTCF	chr4:7169508-7169737	T-47D	breast:	n/a	chr4:7169658-7169679 chr4:7169606-7169619 chr4:7169664-7169680 chr4:7169663-7169681
49	CTCF	chr4:7196260-7196410	GM12870	blood:	n/a	chr4:7196329-7196342 chr4:7196327-7196343 chr4:7196326-7196344 chr4:7196328-7196349 chr4:7196329-7196338
50	CTCF	chr4:7196268-7196396	GM10248	blood:	n/a	chr4:7196329-7196342 chr4:7196327-7196343 chr4:7196326-7196344 chr4:7196328-7196349 chr4:7196329-7196338

(count:1405 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:7195466-7195516	SAEC	small airway:	n/a
2	chr4:7191910-7191960	RPTEC	kidney:	n/a
3	chr4:7195466-7195516	SAEC	small airway:	n/a
4	chr4:7191910-7191960	RPTEC	kidney:	n/a
5	chr4:7187328-7187378	AG04450	lung:	fetal
6	chr4:7193885-7193935	NHDF-neo	bronchial:	n/a
7	chr4:7185889-7185939	T-47D	breast:	n/a
8	chr4:7186138-7186188	SAEC	small airway:	n/a
9	chr4:7196466-7196516	PFSK-1	brain:	n/a
10	chr4:7164648-7164698	GM19239	blood:	n/a
11	chr4:7195002-7195052	NT2-D1	testis:	n/a
12	chr4:7195466-7195516	GM19239	blood:	n/a
13	chr4:7185889-7185939	AG09309	skin:	n/a
14	chr4:7184654-7184704	AG09319	gingival:	n/a
15	chr4:7192699-7192749	BJ	skin:	n/a
16	chr4:7195053-7195103	AG09309	skin:	n/a
17	chr4:7192699-7192749	NH-A	brain:	n/a
18	chr4:7191910-7191960	HL-60	blood:	n/a
19	chr4:7194519-7194569	A549	lung:	n/a
20	chr4:7158489-7158539	HepG2	liver:	n/a
21	chr4:7191910-7191960	HUVEC	blood vessel:	n/a
22	chr4:7164648-7164698	PANC-1	pancreas:	n/a
23	chr4:7187171-7187221	ProgFib	skin:	n/a
24	chr4:7164855-7164905	MCF-7	breast:	n/a
25	chr4:7187328-7187378	PrEC	prostate:	n/a
26	chr4:7185889-7185939	AG10803	skin:	n/a
27	chr4:7187171-7187221	HCM	heart:	n/a
28	chr4:7185889-7185939	AG09319	gingival:	n/a
29	chr4:7184654-7184704	AG04449	skin:	fetal
30	chr4:7193237-7193287	SK-N-SH_RA	brain:	n/a
31	chr4:7184654-7184704	AG09309	skin:	n/a
32	chr4:7185889-7185939	HUVEC	blood vessel:	n/a
33	chr4:7164855-7164905	HEEpiC	esophagus:	n/a
34	chr4:7158489-7158539	GM06990	blood:	n/a
35	chr4:7158489-7158539	HUVEC	blood vessel:	n/a
36	chr4:7192699-7192749	Jurkat	blood:	n/a
37	chr4:7184654-7184704	HIPEpiC	eye:	n/a
38	chr4:7194841-7194891	PANC-1	pancreas:	n/a
39	chr4:7164855-7164905	Hela-S3	cervix:	n/a
40	chr4:7186138-7186188	NB4	blood:	n/a
41	chr4:7193783-7193833	ovcar-3	ovarian:	n/a
42	chr4:7164742-7164792	AG04450	lung:	fetal
43	chr4:7187328-7187378	HNPCEpiC	eye:	n/a
44	chr4:7195053-7195103	IMR90	lung:	fetal
45	chr4:7193237-7193287	AG04450	lung:	fetal
46	chr4:7191910-7191960	ovcar-3	ovarian:	n/a
47	chr4:7194519-7194569	NHDF-neo	bronchial:	n/a
48	chr4:7185164-7185214	H1-hESC	embryonic stem cell:	embryo
49	chr4:7195466-7195516	HMEC	breast:	n/a
50	chr4:7187171-7187221	AG09319	gingival:	n/a

(count:32 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:7196671..7199411-chr4:7206730..7210883,4	MCF-7	breast:
2	chr4:7151546..7154999-chr4:7157110..7159286,3	K562	blood:
3	chr4:7170575..7172996-chr4:7179546..7181445,2	MCF-7	breast:
4	chr4:7179927..7181981-chr4:7190221..7193171,2	MCF-7	breast:
5	chr4:7153142..7154210-chr4:7169124..7170222,3	MCF-7	breast:
6	chr4:7195456..7197409-chr4:7586904..7589269,2	MCF-7	breast:
7	chr4:7155562..7157749-chr4:7159124..7161784,3	K562	blood:
8	chr4:7153303..7154007-chr4:7189364..7189997,2	MCF-7	breast:
9	chr4:7182824..7185399-chr4:7186079..7187991,2	K562	blood:
10	chr4:7195671..7196829-chr4:7297061..7298292,4	MCF-7	breast:
11	chr4:7196173..7199298-chr4:7297617..7300967,3	MCF-7	breast:
12	chr4:7193483..7194227-chr4:7652114..7653022,2	MCF-7	breast:
13	chr4:7156869..7158917-chr4:7168840..7170668,2	K562	blood:
14	chr4:7155562..7157749-chr4:7159124..7161784,3	K562	blood:
15	chr4:7151546..7154999-chr4:7157110..7159286,3	K562	blood:
16	chr4:7196017..7196563-chr4:7337188..7337952,2	MCF-7	breast:
17	chr4:7104610..7105501-chr4:7169229..7170131,2	MCF-7	breast:
18	chr4:7190742..7191404-chr4:7337213..7337934,2	MCF-7	breast:
19	chr4:7179927..7181981-chr4:7190221..7193171,2	MCF-7	breast:
20	chr4:7103774..7104291-chr4:7158329..7158835,2	MCF-7	breast:
21	chr4:7154359..7156507-chr4:7156687..7158772,2	MCF-7	breast:
22	chr4:7182824..7185399-chr4:7186079..7187991,2	K562	blood:
23	chr4:7194853..7196911-chr4:7197699..7199665,2	K562	blood:
24	chr4:7194397..7197077-chr4:7223002..7225801,2	MCF-7	breast:
25	chr4:7156869..7158917-chr4:7168840..7170668,2	K562	blood:
26	chr4:7170575..7172996-chr4:7179546..7181445,2	MCF-7	breast:
27	chr4:7153261..7154139-chr4:7187520..7188707,6	MCF-7	breast:
28	chr4:7103518..7105389-chr4:7163668..7165983,2	K562	blood:
29	chr4:7154359..7156507-chr4:7156687..7158772,2	MCF-7	breast:
30	chr4:7195636..7196730-chr4:7297372..7298445,9	MCF-7	breast:
31	chr4:7191464..7193621-chr4:7207783..7210598,2	MCF-7	breast:
32	chr4:7195064..7196941-chr4:7218562..7221333,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GRPEL1-6	chr4:7155896-7156005	l_2594_chr4:7147195-7156005_prostate

No data

Variant related genes	Relation type
SORCS2	TF binding region
SORCS2	CpG island
ENSG00000245468	chromatin interactions

Extended variants
information (count: 2103 )
Associated
traits (count: 56 )

Variant overlapped rSNPs/rCNVs (count:2103 , 50 per page) page: 1 2 3 4 5 6 7 ... 43

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs3915879	chr4:7154743-7154744	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs117006414	chr4:7154799-7154800	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs114009809	chr4:7154806-7154807	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs115388840	chr4:7154809-7154810	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs528301070	chr4:7154872-7154873	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs546860968	chr4:7154895-7154896	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs561878294	chr4:7154902-7154903	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs73077795	chr4:7154943-7154944	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs550732140	chr4:7154959-7154960	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs369820762	chr4:7154960-7154961	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs6831172	chr4:7154964-7154965	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs149691163	chr4:7154967-7154968	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs6831181	chr4:7154974-7154975	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs369253347	chr4:7155004-7155005	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs566683325	chr4:7155024-7155025	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs558522958	chr4:7155032-7155033	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs11731009	chr4:7155068-7155069	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs11725917	chr4:7155082-7155083	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs574281229	chr4:7155091-7155092	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs148392121	chr4:7155106-7155107	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs11725923	chr4:7155116-7155117	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs142512284	chr4:7155117-7155118	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs545883042	chr4:7155120-7155121	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs13110154	chr4:7155124-7155125	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs75002191	chr4:7155152-7155153	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs564942888	chr4:7155164-7155165	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs532359893	chr4:7155170-7155171	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs540104799	chr4:7155175-7155176	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs562007644	chr4:7155179-7155180	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs529136781	chr4:7155204-7155205	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs73077797	chr4:7155212-7155213	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs562515857	chr4:7155287-7155288	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs187168758	chr4:7155291-7155292	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs189872509	chr4:7155311-7155312	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs180773169	chr4:7155312-7155313	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs185573926	chr4:7155319-7155320	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs534400066	chr4:7155400-7155401	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs549351293	chr4:7155416-7155417	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs567855017	chr4:7155429-7155430	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs190181733	chr4:7155443-7155444	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs61522522	chr4:7155450-7155451	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs556914568	chr4:7155472-7155473	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs568857937	chr4:7155520-7155521	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs539471178	chr4:7155526-7155527	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs557277545	chr4:7155543-7155544	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs371557989	chr4:7155546-7155547	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs557885753	chr4:7155554-7155555	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs182823361	chr4:7155555-7155556	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs540334265	chr4:7155574-7155575	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs555225395	chr4:7155577-7155578	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:56)

Disease	PMID	Source
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
T-cell prolymphocytic leukemia	19278963	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Prostate cancer	18632612	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
Urothelial carcinoma	21177765	CNVD
Myelofibrosis	22110671	CNVD
Hirschsprung''s Disease	21712996	CNVD
Schizophrenia	22241247	CNVD
Autosomal-dominant microtia	18179897	CNVD
Glioma	17123091	CNVD
Colorectal cancer	20459617	CNVD
Breast cancer	17133270	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Cancer	20164919	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:626 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:7105800-7176000	Weak transcription	Right Atrium	heart
2	chr4:7150400-7157400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
3	chr4:7150400-7158800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
4	chr4:7151600-7155600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr4:7152000-7156800	Weak transcription	Colon Smooth Muscle	Colon
6	chr4:7155600-7158000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
7	chr4:7156000-7156600	Bivalent Enhancer	Fetal Muscle Trunk	muscle
8	chr4:7156400-7159400	Enhancers	Fetal Stomach	stomach
9	chr4:7156400-7159800	Enhancers	Fetal Muscle Leg	muscle
10	chr4:7156600-7158200	Enhancers	NHEK	skin
11	chr4:7156600-7159800	Enhancers	Fetal Muscle Trunk	muscle
12	chr4:7156800-7157400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
13	chr4:7156800-7159200	Enhancers	Colon Smooth Muscle	Colon
14	chr4:7157000-7157200	Enhancers	Brain Angular Gyrus	brain
15	chr4:7157000-7157200	Enhancers	Fetal Kidney	kidney
16	chr4:7157000-7157200	Enhancers	Fetal Lung	lung
17	chr4:7157000-7158000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
18	chr4:7157000-7158000	Enhancers	HMEC	breast
19	chr4:7157000-7158200	Enhancers	Skeletal Muscle Male	skeletal muscle
20	chr4:7157000-7158600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
21	chr4:7157000-7158600	Enhancers	K562	blood
22	chr4:7157000-7159000	Enhancers	Rectal Smooth Muscle	rectum
23	chr4:7157000-7159400	Enhancers	Breast Myoepithelial Primary Cells	Breast
24	chr4:7157000-7159800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
25	chr4:7157200-7157800	Enhancers	Rectal Mucosa Donor 31	rectum
26	chr4:7157200-7158000	Weak transcription	Fetal Lung	lung
27	chr4:7157200-7158000	Enhancers	Fetal Thymus	thymus
28	chr4:7157200-7158200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
29	chr4:7157200-7158200	Weak transcription	Fetal Kidney	kidney
30	chr4:7157200-7158400	Enhancers	Esophagus	oesophagus
31	chr4:7157200-7158400	Enhancers	Fetal Intestine Large	intestine
32	chr4:7157200-7158400	Enhancers	Fetal Intestine Small	intestine
33	chr4:7157200-7158400	Enhancers	Rectal Mucosa Donor 29	rectum
34	chr4:7157200-7158400	Enhancers	Skeletal Muscle Female	skeletal muscle
35	chr4:7157200-7158400	Enhancers	HUVEC	blood vessel
36	chr4:7157200-7158800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
37	chr4:7157200-7159200	Enhancers	Ovary	ovary
38	chr4:7157200-7159400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
39	chr4:7157400-7157600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
40	chr4:7157400-7157800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
41	chr4:7157400-7157800	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
42	chr4:7157400-7157800	Enhancers	NH-A	brain
43	chr4:7157400-7158200	Bivalent Enhancer	HepG2	liver
44	chr4:7157400-7159000	Enhancers	Stomach Smooth Muscle	stomach
45	chr4:7157600-7157800	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin
46	chr4:7157600-7157800	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
47	chr4:7157600-7157800	Bivalent Enhancer	Adipose Nuclei	Adipose
48	chr4:7157600-7157800	Enhancers	Spleen	Spleen
49	chr4:7157600-7158000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
50	chr4:7157600-7158000	Bivalent Enhancer	Placenta	Placenta

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