Variant report

Variant	esv1848625
Chromosome Location	chr4:20760089-20821762
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	ARID3A	chr4:20775077-20775342	HepG2	liver:	n/a	n/a
2	BACH1	chr4:20817391-20817392	H1-hESC	embryonic stem cell:	n/a	n/a
3	BHLHE40	chr4:20775048-20775386	HepG2	liver:	n/a	n/a
4	BHLHE40	chr4:20811465-20811810	HepG2	liver:	n/a	n/a
5	CEBPB	chr4:20814041-20814294	HepG2	liver:	n/a	chr4:20814155-20814166
6	CEBPB	chr4:20798521-20798728	HepG2	liver:	n/a	chr4:20798642-20798653
7	CEBPB	chr4:20797177-20797386	A549	lung:	n/a	chr4:20797259-20797272 chr4:20797259-20797270
8	CEBPB	chr4:20800556-20800817	HepG2	liver:	n/a	chr4:20800688-20800699 chr4:20800653-20800664
9	CEBPB	chr4:20788544-20788846	HepG2	liver:	n/a	chr4:20788712-20788723 chr4:20788714-20788723 chr4:20788713-20788724 chr4:20788714-20788723 chr4:20788714-20788723 chr4:20788714-20788723
10	CEBPB	chr4:20814036-20814312	IMR90	lung:	n/a	chr4:20814155-20814166
11	CEBPB	chr4:20797109-20797407	HepG2	liver:	n/a	chr4:20797259-20797272 chr4:20797259-20797270
12	CHD2	chr4:20775018-20775331	H1-hESC	embryonic stem cell:	n/a	n/a
13	CTCF	chr4:20775120-20775270	GM12868	blood:	n/a	chr4:20775211-20775232 chr4:20775212-20775225 chr4:20775209-20775227
14	CTCF	chr4:20761860-20762010	GM12873	blood:	n/a	chr4:20761860-20761876
15	CTCF	chr4:20761760-20761910	HVMF	connective:	n/a	chr4:20761860-20761876
16	CTCF	chr4:20775085-20775355	GM12878	blood:	n/a	chr4:20775211-20775232 chr4:20775212-20775225 chr4:20775209-20775227
17	CTCF	chr4:20775160-20775310	HPAF	blood vessel:	n/a	chr4:20775211-20775232 chr4:20775212-20775225 chr4:20775209-20775227
18	CTCF	chr4:20775160-20775310	NHDF-neo	bronchial:	n/a	chr4:20775211-20775232 chr4:20775212-20775225 chr4:20775209-20775227
19	CTCF	chr4:20768063-20768152	GM10248	blood:	n/a	n/a
20	CTCF	chr4:20775120-20775270	GM12864	blood:	n/a	chr4:20775211-20775232 chr4:20775212-20775225 chr4:20775209-20775227
21	CTCF	chr4:20775096-20775333	Kidney_OC	kidney:	n/a	chr4:20775211-20775232 chr4:20775212-20775225 chr4:20775209-20775227
22	CTCF	chr4:20775180-20775330	GM12878	blood:	n/a	chr4:20775211-20775232 chr4:20775212-20775225 chr4:20775209-20775227
23	CTCF	chr4:20775100-20775250	GM12864	blood:	n/a	chr4:20775211-20775232 chr4:20775212-20775225 chr4:20775209-20775227
24	CTCF	chr4:20775081-20775330	K562	blood:	n/a	chr4:20775211-20775232 chr4:20775212-20775225 chr4:20775209-20775227
25	CTCF	chr4:20775092-20775296	A549	lung:	n/a	chr4:20775211-20775232 chr4:20775212-20775225 chr4:20775209-20775227
26	CTCF	chr4:20775120-20775270	HCFaa	heart:	n/a	chr4:20775211-20775232 chr4:20775212-20775225 chr4:20775209-20775227
27	CTCF	chr4:20775160-20775310	AG10803	skin:	n/a	chr4:20775211-20775232 chr4:20775212-20775225 chr4:20775209-20775227
28	CTCF	chr4:20775160-20775310	GM12866	blood:	n/a	chr4:20775211-20775232 chr4:20775212-20775225 chr4:20775209-20775227
29	CTCF	chr4:20761841-20761890	GM10266	blood:	n/a	chr4:20761860-20761876
30	CTCF	chr4:20761820-20761970	RPTEC	kidney:	n/a	chr4:20761860-20761876
31	CTCF	chr4:20761780-20761930	BE2_C	brain:	n/a	chr4:20761860-20761876
32	CTCF	chr4:20761820-20761970	AG10803	skin:	n/a	chr4:20761860-20761876
33	CTCF	chr4:20761795-20761940	HepG2	liver:	n/a	chr4:20761860-20761876
34	CTCF	chr4:20775081-20775308	GM10248	blood:	n/a	chr4:20775211-20775232 chr4:20775212-20775225 chr4:20775209-20775227
35	CTCF	chr4:20774460-20774610	AG09319	gingival:	n/a	n/a
36	CTCF	chr4:20775480-20775630	GM12867	blood:	n/a	n/a
37	CTCF	chr4:20774971-20775417	GM12878	blood:	n/a	chr4:20775211-20775232 chr4:20775212-20775225 chr4:20775209-20775227
38	CTCF	chr4:20775100-20775250	HepG2	liver:	n/a	chr4:20775211-20775232 chr4:20775212-20775225 chr4:20775209-20775227
39	CTCF	chr4:20775140-20775290	Hela-S3	cervix:	n/a	chr4:20775211-20775232 chr4:20775212-20775225 chr4:20775209-20775227
40	CTCF	chr4:20761780-20761930	GM12868	blood:	n/a	chr4:20761860-20761876
41	CTCF	chr4:20775140-20775290	GM12874	blood:	n/a	chr4:20775211-20775232 chr4:20775212-20775225 chr4:20775209-20775227
42	CTCF	chr4:20761740-20761890	GM12878	blood:	n/a	chr4:20761860-20761876
43	CTCF	chr4:20761767-20761971	MCF-7	breast:	n/a	chr4:20761860-20761876
44	CTCF	chr4:20775140-20775290	NHEK	skin:	n/a	chr4:20775211-20775232 chr4:20775212-20775225 chr4:20775209-20775227
45	CTCF	chr4:20774966-20775452	MCF-7	breast:	n/a	chr4:20775211-20775232 chr4:20775212-20775225 chr4:20775209-20775227
46	CTCF	chr4:20775120-20775270	SAEC	small airway:	n/a	chr4:20775211-20775232 chr4:20775212-20775225 chr4:20775209-20775227
47	CTCF	chr4:20761760-20761910	HEK293	kidney:	n/a	chr4:20761860-20761876
48	CTCF	chr4:20761800-20761950	Caco-2	colon:	n/a	chr4:20761860-20761876
49	CTCF	chr4:20761760-20761910	Caco-2	colon:	n/a	chr4:20761860-20761876
50	CTCF	chr4:20775140-20775290	AG10803	skin:	n/a	chr4:20775211-20775232 chr4:20775212-20775225 chr4:20775209-20775227

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:20811042-20811092	HAEpiC	amniotic membrane:	n/a
2	chr4:20811042-20811092	U87	brain:	n/a
3	chr4:20811042-20811092	H1-hESC	embryonic stem cell:	embryo
4	chr4:20811042-20811092	PANC-1	pancreas:	n/a
5	chr4:20811042-20811092	MCF10A-Er-Src	breast:	n/a
6	chr4:20811042-20811092	NT2-D1	testis:	n/a
7	chr4:20811042-20811092	GM12891	blood:	n/a
8	chr4:20811042-20811092	HCT-116	colon:	n/a
9	chr4:20811042-20811092	NHBE	bronchial:	n/a
10	chr4:20811042-20811092	PrEC	prostate:	n/a
11	chr4:20811042-20811092	HRPEpiC	eye:	n/a
12	chr4:20811042-20811092	AG10803	skin:	n/a
13	chr4:20811042-20811092	Jurkat	blood:	n/a
14	chr4:20811042-20811092	HNPCEpiC	eye:	n/a
15	chr4:20811042-20811092	K562	blood:	n/a
16	chr4:20811042-20811092	Hela-S3	cervix:	n/a
17	chr4:20811042-20811092	RPTEC	kidney:	n/a
18	chr4:20811042-20811092	SK-N-SH	brain:	n/a
19	chr4:20811042-20811092	SAEC	small airway:	n/a
20	chr4:20811042-20811092	HEEpiC	esophagus:	n/a
21	chr4:20811042-20811092	SK-N-MC	brain:	n/a
22	chr4:20811042-20811092	HEK293	kidney:	embryo
23	chr4:20811042-20811092	IMR90	lung:	fetal
24	chr4:20811042-20811092	SK-N-SH_RA	brain:	n/a
25	chr4:20811042-20811092	LNCaP	prostate:	n/a
26	chr4:20811042-20811092	GM12892	blood:	n/a
27	chr4:20811042-20811092	AG09309	skin:	n/a
28	chr4:20811042-20811092	HCM	heart:	n/a
29	chr4:20811042-20811092	BJ	skin:	n/a
30	chr4:20811042-20811092	HCF	heart:	n/a
31	chr4:20811042-20811092	HIPEpiC	eye:	n/a
32	chr4:20811042-20811092	HRE	kidney:	n/a
33	chr4:20811042-20811092	PFSK-1	brain:	n/a
34	chr4:20811042-20811092	Hepatocyte	liver:	n/a
35	chr4:20811042-20811092	AG04449	skin:	fetal
36	chr4:20811042-20811092	ovcar-3	ovarian:	n/a
37	chr4:20811042-20811092	AG04450	lung:	fetal
38	chr4:20811042-20811092	AG09319	gingival:	n/a
39	chr4:20811042-20811092	A549	lung:	n/a
40	chr4:20811042-20811092	GM19239	blood:	n/a
41	chr4:20811042-20811092	AoSMC	blood vessel:	n/a
42	chr4:20811042-20811092	BE2_C	brain:	n/a
43	chr4:20811042-20811092	Caco-2	colon:	n/a
44	chr4:20811042-20811092	GM12878	blood:	n/a
45	chr4:20811042-20811092	HMEC	breast:	n/a
46	chr4:20811042-20811092	CMK	blood:	n/a
47	chr4:20811042-20811092	NB4	blood:	n/a
48	chr4:20811042-20811092	NH-A	brain:	n/a
49	chr4:20811042-20811092	HPAEpiC	pulmonary alveolar:	n/a
50	chr4:20811042-20811092	ProgFib	skin:	n/a

No.	Distal block	Cell Line	Cell type
1	chr4:20791958..20793489-chr4:20799634..20802311,2	K562	blood:
2	chr4:20791958..20793489-chr4:20799634..20802311,2	K562	blood:
3	chr4:20758225..20761110-chr4:20761707..20763289,2	MCF-7	breast:
4	chr4:20774939..20775520-chr4:21136553..21137202,2	MCF-7	breast:
5	chr4:20779088..20780993-chr4:20896835..20899396,2	K562	blood:
6	chr4:20756151..20758021-chr4:20765219..20767901,2	K562	blood:
7	chr4:20759824..20762284-chr4:20763447..20765411,2	K562	blood:
8	chr4:20776494..20778419-chr4:20785252..20787706,2	K562	blood:
9	chr4:20759824..20762284-chr4:20763447..20765411,2	K562	blood:
10	chr4:20758225..20761110-chr4:20761707..20763289,2	MCF-7	breast:
11	chr4:20776494..20778419-chr4:20785252..20787706,2	K562	blood:
12	chr4:20774749..20775678-chr4:21136384..21137379,5	MCF-7	breast:
13	chr4:20774692..20775734-chr4:21470776..21471557,3	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PACRGL-6	chr4:20768431-20768995	ENSG00000272995.1

Variant related genes	Relation type
ENSG00000272995	TF binding region
ENSG00000272995	CpG island

Extended variants
information (count: 1599 )
Associated
traits (count: 64 )

Variant overlapped rSNPs/rCNVs (count:1599 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4697177	chr4:20760089-20760090	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs573889413	chr4:20760118-20760119	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs540921778	chr4:20760120-20760121	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs188981999	chr4:20760123-20760124	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs550565068	chr4:20760186-20760187	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs532929539	chr4:20760237-20760238	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs6447982	chr4:20760238-20760239	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs563073588	chr4:20760264-20760265	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs530509956	chr4:20760273-20760274	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs548969424	chr4:20760355-20760356	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs139642771	chr4:20760387-20760388	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs370821396	chr4:20760412-20760413	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs149751928	chr4:20760414-20760415	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs372164547	chr4:20760417-20760418	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs200980103	chr4:20760422-20760423	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs77824213	chr4:20760424-20760425	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs571953101	chr4:20760438-20760439	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs367827327	chr4:20760453-20760454	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs373534338	chr4:20760481-20760482	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs148511080	chr4:20760520-20760521	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs200213619	chr4:20760521-20760522	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs75535060	chr4:20760540-20760541	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs536310590	chr4:20760544-20760545	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs554952304	chr4:20760551-20760552	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs573129011	chr4:20760552-20760553	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs540944595	chr4:20760553-20760554	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs559259503	chr4:20760559-20760560	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs577496333	chr4:20760595-20760596	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs57740160	chr4:20760644-20760645	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs570576735	chr4:20760682-20760683	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs17623902	chr4:20760683-20760684	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs548773644	chr4:20760705-20760706	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs146591398	chr4:20760732-20760733	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs528106787	chr4:20760785-20760786	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs546597227	chr4:20760802-20760803	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs572016659	chr4:20760815-20760816	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs193112688	chr4:20760835-20760836	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs551205935	chr4:20760851-20760852	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs141346106	chr4:20760853-20760854	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs184332207	chr4:20760859-20760860	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs112388861	chr4:20760869-20760870	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs74475192	chr4:20760870-20760871	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs554734683	chr4:20760892-20760893	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs566942722	chr4:20760903-20760904	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs189181866	chr4:20760909-20760910	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs558527629	chr4:20760921-20760922	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs143837218	chr4:20760940-20760941	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs544853729	chr4:20760979-20760980	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs557139736	chr4:20761022-20761023	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs181053891	chr4:20761027-20761028	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:64)

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
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	22183965	CNVD
Multiple myeloma	17550852	CNVD
Prostate cancer	18632612	CNVD
Ovarian cancer	17908972	CNVD
Olfactory neuroblastoma	18408657	CNVD
Burkitt''s lymphoma	20823134	CNVD
Burkitt''s lymphoma	19759907	CNVD
Myelofibrosis	22110671	CNVD
Colorectal cancer	16774939	CNVD
Breast cancer	22522925	CNVD
Breast cancer	22737080	CNVD
Lung squamous cell carcinoma	22363434	CNVD
Pancreatic cancer	17952125	CNVD
Cancer	20164919	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Glioma	20126413	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:103 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:20739200-20761200	Weak transcription	Fetal Heart	heart
2	chr4:20740600-20763600	Weak transcription	Brain Anterior Caudate	brain
3	chr4:20740800-20763600	Weak transcription	HSMMtube	muscle
4	chr4:20740800-20770600	Weak transcription	Brain Inferior Temporal Lobe	brain
5	chr4:20740800-20791200	Weak transcription	Ovary	ovary
6	chr4:20746800-20761400	Weak transcription	Aorta	Aorta
7	chr4:20746800-20775000	Weak transcription	Left Ventricle	heart
8	chr4:20749600-20763800	Weak transcription	Brain Germinal Matrix	brain
9	chr4:20753000-20760400	Weak transcription	Primary hematopoietic stem cells	blood
10	chr4:20755800-20761600	Weak transcription	Fetal Lung	lung
11	chr4:20757000-20763800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
12	chr4:20760400-20760600	Enhancers	Primary hematopoietic stem cells	blood
13	chr4:20761400-20761600	ZNF genes & repeats	Aorta	Aorta
14	chr4:20761600-20761800	Active TSS	Fetal Lung	lung
15	chr4:20761600-20762600	Weak transcription	Aorta	Aorta
16	chr4:20763600-20763800	Enhancers	Brain Anterior Caudate	brain
17	chr4:20774800-20775000	Weak transcription	Brain Angular Gyrus	brain
18	chr4:20774800-20775000	Active TSS	NHEK	skin
19	chr4:20775000-20775200	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Female	--
20	chr4:20775000-20775200	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Male	--
21	chr4:20775000-20775200	Enhancers	Muscle Satellite Cultured Cells	--
22	chr4:20775000-20775200	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
23	chr4:20775000-20775200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
24	chr4:20775000-20775200	Enhancers	Liver	Liver
25	chr4:20775000-20775200	Flanking Active TSS	Brain Angular Gyrus	brain
26	chr4:20775000-20775200	Enhancers	Brain Anterior Caudate	brain
27	chr4:20775000-20775200	Enhancers	Brain Hippocampus Middle	brain
28	chr4:20775000-20775200	Enhancers	Left Ventricle	heart
29	chr4:20775000-20775200	Enhancers	NH-A	brain
30	chr4:20775000-20775200	Flanking Active TSS	NHEK	skin
31	chr4:20775000-20775200	Enhancers	Osteobl	bone
32	chr4:20775000-20775400	Bivalent/Poised TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
33	chr4:20775000-20775400	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
34	chr4:20775000-20775400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
35	chr4:20775000-20775600	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
36	chr4:20775000-20775600	Enhancers	Primary T helper cells fromperipheralblood	blood
37	chr4:20775000-20775800	Enhancers	Primary T helper naive cells from peripheral blood	blood
38	chr4:20775000-20775800	Enhancers	Rectal Smooth Muscle	rectum
39	chr4:20775000-20775800	Enhancers	HUVEC	blood vessel
40	chr4:20775000-20776400	Enhancers	Colon Smooth Muscle	Colon
41	chr4:20775200-20775400	Active TSS	Brain Angular Gyrus	brain
42	chr4:20775800-20777800	Weak transcription	HUVEC	blood vessel
43	chr4:20776200-20776600	Enhancers	Fetal Kidney	kidney
44	chr4:20777800-20778200	Enhancers	HUVEC	blood vessel
45	chr4:20778200-20779200	Weak transcription	HUVEC	blood vessel
46	chr4:20779200-20781200	Enhancers	HUVEC	blood vessel
47	chr4:20781200-20781400	Weak transcription	HUVEC	blood vessel
48	chr4:20788600-20788800	Enhancers	Colon Smooth Muscle	Colon
49	chr4:20788800-20790000	Weak transcription	Colon Smooth Muscle	Colon
50	chr4:20789600-20790200	Enhancers	Brain Germinal Matrix	brain

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