Variant report

Variant	esv2757924
Chromosome Location	chr4:21873204-21980559
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr4:21949958-21950354	H1-hESC	embryonic stem cell:	n/a	n/a
2	BHLHE40	chr4:21954226-21954407	GM12878	blood:	n/a	n/a
3	BHLHE40	chr4:21889774-21889826	GM12878	blood:	n/a	n/a
4	CEBPB	chr4:21889772-21890188	IMR90	lung:	n/a	chr4:21889952-21889965
5	CEBPB	chr4:21964808-21965023	H1-hESC	embryonic stem cell:	n/a	chr4:21964939-21964950
6	CEBPB	chr4:21899779-21900104	HepG2	liver:	n/a	chr4:21899942-21899953
7	CEBPB	chr4:21964793-21965076	HepG2	liver:	n/a	chr4:21964939-21964950
8	CEBPB	chr4:21899762-21900114	A549	lung:	n/a	chr4:21899942-21899953
9	CEBPB	chr4:21917207-21917372	HepG2	liver:	n/a	chr4:21917324-21917335
10	CEBPB	chr4:21899910-21900079	K562	blood:	n/a	chr4:21899942-21899953
11	CEBPB	chr4:21886891-21887197	IMR90	lung:	n/a	chr4:21887024-21887037 chr4:21887026-21887037 chr4:21887026-21887037 chr4:21887024-21887037
12	CEBPB	chr4:21899776-21900121	H1-hESC	embryonic stem cell:	n/a	chr4:21899942-21899953
13	CEBPB	chr4:21964849-21965102	IMR90	lung:	n/a	chr4:21964939-21964950
14	CEBPB	chr4:21899766-21900120	IMR90	lung:	n/a	chr4:21899942-21899953
15	CHD2	chr4:21962848-21962867	H1-hESC	embryonic stem cell:	n/a	n/a
16	CHD2	chr4:21954213-21954397	GM12878	blood:	n/a	n/a
17	CHD2	chr4:21949928-21950234	H1-hESC	embryonic stem cell:	n/a	n/a
18	CTBP2	chr4:21950634-21951259	H1-hESC	embryonic stem cell:	n/a	n/a
19	CTCF	chr4:21950100-21950250	HBMEC	blood vessel:	n/a	n/a
20	CTCF	chr4:21880990-21881149	HepG2	liver:	n/a	chr4:21881058-21881079 chr4:21881063-21881081 chr4:21881065-21881078
21	CTCF	chr4:21881000-21881150	HCPEpiC	choroid plexus:	n/a	chr4:21881058-21881079 chr4:21881063-21881081 chr4:21881065-21881078
22	CTCF	chr4:21949895-21951210	SK-N-SH	brain:	n/a	chr4:21950602-21950620 chr4:21950604-21950617
23	CTCF	chr4:21881035-21881126	GM19238	blood:	n/a	chr4:21881058-21881079 chr4:21881063-21881081 chr4:21881065-21881078
24	CTCF	chr4:21950082-21950250	Fibrobl	skin:	n/a	n/a
25	CTCF	chr4:21950243-21950532	H1-hESC	embryonic stem cell:	n/a	n/a
26	CTCF	chr4:21880970-21881179	HepG2	liver:	n/a	chr4:21881058-21881079 chr4:21881063-21881081 chr4:21881065-21881078
27	CTCF	chr4:21907954-21908048	ProgFib	skin:	n/a	n/a
28	CTCF	chr4:21880980-21881130	AG04450	lung:	n/a	chr4:21881058-21881079 chr4:21881063-21881081 chr4:21881065-21881078
29	CTCF	chr4:21881005-21881113	NHEK	skin:	n/a	chr4:21881058-21881079 chr4:21881063-21881081 chr4:21881065-21881078
30	CTCF	chr4:21880978-21881143	MCF-7	breast:	n/a	chr4:21881058-21881079 chr4:21881063-21881081 chr4:21881065-21881078
31	CTCF	chr4:21880937-21881200	H1-hESC	embryonic stem cell:	n/a	chr4:21881058-21881079 chr4:21881063-21881081 chr4:21881065-21881078
32	CTCF	chr4:21950260-21950488	Fibrobl	skin:	n/a	n/a
33	CTCF	chr4:21881020-21881170	AG09319	gingival:	n/a	chr4:21881058-21881079 chr4:21881063-21881081 chr4:21881065-21881078
34	CTCF	chr4:21881020-21881170	HCPEpiC	choroid plexus:	n/a	chr4:21881058-21881079 chr4:21881063-21881081 chr4:21881065-21881078
35	CTCF	chr4:21881020-21881170	HRE	kidney:	n/a	chr4:21881058-21881079 chr4:21881063-21881081 chr4:21881065-21881078
36	CTCF	chr4:21950320-21950470	HepG2	liver:	n/a	n/a
37	CTCF	chr4:21950360-21950510	HMEC	breast:	n/a	n/a
38	CTCF	chr4:21950312-21950567	H1-hESC	embryonic stem cell:	n/a	n/a
39	CTCF	chr4:21880980-21881130	HMF	breast:	n/a	chr4:21881058-21881079 chr4:21881063-21881081 chr4:21881065-21881078
40	CTCF	chr4:21950346-21950479	ProgFib	skin:	n/a	n/a
41	CTCF	chr4:21950120-21950270	AG04449	skin:	n/a	n/a
42	CTCF	chr4:21950160-21950310	RPTEC	kidney:	n/a	n/a
43	CTCF	chr4:21950140-21950290	AoAF	blood vessel:	n/a	n/a
44	CTCF	chr4:21962740-21962890	GM12867	blood:	n/a	n/a
45	CTCF	chr4:21881040-21881310	HCT-116	colon:	n/a	chr4:21881058-21881079 chr4:21881063-21881081 chr4:21881065-21881078
46	CTCF	chr4:21950300-21950450	AG09319	gingival:	n/a	n/a
47	CTCF	chr4:21880928-21881204	Gliobla	brain:	n/a	chr4:21881058-21881079 chr4:21881063-21881081 chr4:21881065-21881078
48	CTCF	chr4:21880980-21881130	A549	lung:	n/a	chr4:21881058-21881079 chr4:21881063-21881081 chr4:21881065-21881078
49	CTCF	chr4:21950300-21950450	HRPEpiC	eye:	n/a	n/a
50	CTCF	chr4:21950433-21950450	HepG2	liver:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:21950952-21951002	LNCaP	prostate:	n/a
2	chr4:21951046-21951096	K562	blood:	n/a
3	chr4:21950864-21950914	GM12891	blood:	n/a
4	chr4:21974932-21974982	PrEC	prostate:	n/a
5	chr4:21974932-21974982	GM19239	blood:	n/a
6	chr4:21950155-21950205	HEK293	kidney:	embryo
7	chr4:21951046-21951096	AoSMC	blood vessel:	n/a
8	chr4:21949853-21949903	HEEpiC	esophagus:	n/a
9	chr4:21950952-21951002	GM12891	blood:	n/a
10	chr4:21950722-21950772	RPTEC	kidney:	n/a
11	chr4:21953738-21953788	CMK	blood:	n/a
12	chr4:21949853-21949903	SK-N-SH_RA	brain:	n/a
13	chr4:21953738-21953788	Hepatocyte	liver:	n/a
14	chr4:21950766-21950816	LNCaP	prostate:	n/a
15	chr4:21950567-21950617	AoSMC	blood vessel:	n/a
16	chr4:21951046-21951096	IMR90	lung:	fetal
17	chr4:21950173-21950223	HL-60	blood:	n/a
18	chr4:21950722-21950772	NHBE	bronchial:	n/a
19	chr4:21950952-21951002	AG04450	lung:	fetal
20	chr4:21949853-21949903	H1-hESC	embryonic stem cell:	embryo
21	chr4:21953738-21953788	PFSK-1	brain:	n/a
22	chr4:21950173-21950223	GM06990	blood:	n/a
23	chr4:21950155-21950205	U87	brain:	n/a
24	chr4:21951046-21951096	ProgFib	skin:	n/a
25	chr4:21949853-21949903	LNCaP	prostate:	n/a
26	chr4:21950173-21950223	HNPCEpiC	eye:	n/a
27	chr4:21953738-21953788	ovcar-3	ovarian:	n/a
28	chr4:21950864-21950914	NHDF-neo	bronchial:	n/a
29	chr4:21950722-21950772	HCF	heart:	n/a
30	chr4:21950864-21950914	HUVEC	blood vessel:	n/a
31	chr4:21950952-21951002	HepG2	liver:	n/a
32	chr4:21950173-21950223	SK-N-SH_RA	brain:	n/a
33	chr4:21974932-21974982	IMR90	lung:	fetal
34	chr4:21950722-21950772	HRPEpiC	eye:	n/a
35	chr4:21951046-21951096	Jurkat	blood:	n/a
36	chr4:21951046-21951096	NH-A	brain:	n/a
37	chr4:21953738-21953788	HCT-116	colon:	n/a
38	chr4:21950155-21950205	HCPEpiC	choroid plexus:	n/a
39	chr4:21974932-21974982	HRCEpiC	kidney:	n/a
40	chr4:21950952-21951002	GM19239	blood:	n/a
41	chr4:21951046-21951096	GM12878	blood:	n/a
42	chr4:21950766-21950816	H1-hESC	embryonic stem cell:	embryo
43	chr4:21950766-21950816	HRCEpiC	kidney:	n/a
44	chr4:21950864-21950914	SAEC	small airway:	n/a
45	chr4:21950155-21950205	HAEpiC	amniotic membrane:	n/a
46	chr4:21974932-21974982	GM06990	blood:	n/a
47	chr4:21950952-21951002	NB4	blood:	n/a
48	chr4:21947400-21947450	HEEpiC	esophagus:	n/a
49	chr4:21950864-21950914	ECC-1	luminal epithelium:	n/a
50	chr4:21950155-21950205	HRE	kidney:	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr2:186966503..186967236-chr4:21954917..21955427,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PACRGL-5	chr4:21950638-21951082	ENSG00000250039.2
2	lnc-PACRGL-5	chr4:21950638-21951082	ENSG00000250039.3

Variant related genes	Relation type
ENSG00000250039	TF binding region
KCNIP4	TF binding region
ENSG00000250039	CpG island
KCNIP4	CpG island

Extended variants
information (count: 1764 )
Associated
traits (count: 60 )

Variant overlapped rSNPs/rCNVs (count:1764 , 50 per page) page: 1 2 3 4 5 6 7 ... 36

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs545156203	chr4:21873305-21873306	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs563324387	chr4:21873413-21873414	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs113113241	chr4:21873449-21873450	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs530764806	chr4:21873502-21873503	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs373397644	chr4:21873556-21873557	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs376920051	chr4:21873607-21873608	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs377422610	chr4:21873609-21873610	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs201010094	chr4:21873651-21873652	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs529209438	chr4:21873677-21873678	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs547391430	chr4:21873710-21873711	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs185481948	chr4:21873722-21873723	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs537604587	chr4:21873738-21873739	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs370194352	chr4:21873822-21873823	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs566005958	chr4:21873877-21873878	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs190783921	chr4:21873891-21873892	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs558450818	chr4:21873899-21873900	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs182173879	chr4:21873969-21873970	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs537691410	chr4:21874017-21874018	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs550405924	chr4:21874024-21874025	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs555459396	chr4:21874059-21874060	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs28600835	chr4:21874077-21874078	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs532861398	chr4:21874078-21874079	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs552255129	chr4:21874105-21874106	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs115449953	chr4:21874125-21874126	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs553017975	chr4:21874150-21874151	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs377435570	chr4:21874165-21874166	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs34008037	chr4:21874166-21874167	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs544954477	chr4:21874193-21874194	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs183517599	chr4:21874334-21874335	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs150085612	chr4:21874368-21874369	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs542817681	chr4:21874385-21874386	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs13110177	chr4:21874398-21874399	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs529369817	chr4:21874413-21874414	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs548323207	chr4:21874452-21874453	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs188160248	chr4:21874464-21874465	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs559299436	chr4:21874470-21874471	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs533409840	chr4:21874579-21874580	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs551777191	chr4:21874617-21874618	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs181049470	chr4:21874643-21874644	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs537198892	chr4:21874685-21874686	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs549617385	chr4:21874750-21874751	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs117774203	chr4:21874775-21874776	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs567116679	chr4:21874842-21874843	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs536003874	chr4:21874850-21874851	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs555944603	chr4:21874889-21874890	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs553134445	chr4:21874918-21874919	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs370513630	chr4:21875027-21875028	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs538672069	chr4:21875031-21875032	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs556935461	chr4:21875057-21875058	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs573514070	chr4:21875065-21875066	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:60)

Disease	PMID	Source
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
Oral squamous cell carcinoma	17134496	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
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
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	16608533	CNVD
Non-small cell lung cancer	21829676	CNVD
Melanoma	22183965	CNVD
Multiple myeloma	17550852	CNVD
Prostate cancer	18632612	CNVD
Olfactory neuroblastoma	18408657	CNVD
Burkitt''s lymphoma	20823134	CNVD
Burkitt''s lymphoma	19759907	CNVD
Myelofibrosis	22110671	CNVD
Colorectal cancer	16774939	CNVD
Cancer	22183965	CNVD
Gastric cancer	16891809	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:385 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:21862600-21875000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr4:21872400-21873400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
3	chr4:21872400-21873600	Weak transcription	Fetal Heart	heart
4	chr4:21872400-21873800	Weak transcription	HUES48 Cell Line	embryonic stem cell
5	chr4:21873600-21873800	Enhancers	iPS-20b Cell Line	embryonic stem cell
6	chr4:21873600-21874000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
7	chr4:21873600-21874400	Enhancers	Fetal Heart	heart
8	chr4:21873800-21874000	Enhancers	HUES48 Cell Line	embryonic stem cell
9	chr4:21874000-21875600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
10	chr4:21874400-21879200	Weak transcription	Fetal Heart	heart
11	chr4:21874600-21875600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
12	chr4:21874600-21876000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
13	chr4:21874800-21875800	Enhancers	Muscle Satellite Cultured Cells	--
14	chr4:21875000-21875600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
15	chr4:21875200-21875400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
16	chr4:21875600-21876000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
17	chr4:21875600-21880800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
18	chr4:21875800-21880600	Weak transcription	Muscle Satellite Cultured Cells	--
19	chr4:21879200-21879400	Enhancers	Fetal Heart	heart
20	chr4:21880600-21881200	Enhancers	Muscle Satellite Cultured Cells	--
21	chr4:21880600-21881200	Enhancers	Osteobl	bone
22	chr4:21880800-21881200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
23	chr4:21881000-21881200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
24	chr4:21881200-21883200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
25	chr4:21881200-21883400	Weak transcription	Muscle Satellite Cultured Cells	--
26	chr4:21881200-21883800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
27	chr4:21881200-21886400	Weak transcription	Osteobl	bone
28	chr4:21882400-21882600	Enhancers	HMEC	breast
29	chr4:21882800-21884200	Weak transcription	HMEC	breast
30	chr4:21883200-21884400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
31	chr4:21883400-21884200	Enhancers	Muscle Satellite Cultured Cells	--
32	chr4:21883600-21883800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
33	chr4:21883600-21884000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
34	chr4:21883600-21884600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
35	chr4:21883800-21884000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
36	chr4:21883800-21884400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
37	chr4:21883800-21886400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
38	chr4:21884000-21886400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
39	chr4:21884000-21888800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
40	chr4:21884200-21885200	Enhancers	HMEC	breast
41	chr4:21884200-21886600	Weak transcription	Muscle Satellite Cultured Cells	--
42	chr4:21884400-21886200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
43	chr4:21884600-21888800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
44	chr4:21885200-21888800	Weak transcription	HMEC	breast
45	chr4:21886200-21891600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
46	chr4:21886400-21887200	Enhancers	Osteobl	bone
47	chr4:21886400-21887600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
48	chr4:21886400-21887800	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
49	chr4:21886600-21888000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
50	chr4:21886600-21890200	Enhancers	Muscle Satellite Cultured Cells	--

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