Variant report

Variant	nsv461645
Chromosome Location	chr4:133160255-133293122
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	chr4:133266134-133266306	K562	blood:	n/a	n/a
2	BATF	chr4:133162291-133162510	GM12878	blood:	n/a	n/a
3	BATF	chr4:133162320-133162585	GM12878	blood:	n/a	n/a
4	BHLHE40	chr4:133265695-133265813	K562	blood:	n/a	n/a
5	BHLHE40	chr4:133264871-133264883	K562	blood:	n/a	n/a
6	BHLHE40	chr4:133266102-133266846	K562	blood:	n/a	n/a
7	BRCA1	chr4:133266159-133266384	Hela-S3	cervix:	n/a	n/a
8	CBX3	chr4:133265310-133265941	K562	blood:	n/a	n/a
9	CBX3	chr4:133266054-133266694	K562	blood:	n/a	n/a
10	CCNT2	chr4:133266111-133266381	K562	blood:	n/a	n/a
11	CEBPB	chr4:133254850-133255208	Hela-S3	cervix:	n/a	n/a
12	CEBPB	chr4:133240140-133240393	HepG2	liver:	n/a	chr4:133240209-133240220 chr4:133240188-133240199 chr4:133240209-133240222
13	CEBPB	chr4:133266193-133266232	K562	blood:	n/a	n/a
14	CEBPB	chr4:133254553-133255549	IMR90	lung:	n/a	chr4:133254713-133254724 chr4:133254713-133254726
15	CEBPB	chr4:133278703-133278936	ECC-1	luminal epithelium:	n/a	chr4:133278842-133278859
16	CEBPB	chr4:133234404-133234637	HepG2	liver:	n/a	n/a
17	CEBPB	chr4:133228257-133228566	HepG2	liver:	n/a	chr4:133228409-133228420
18	CEBPB	chr4:133246117-133246325	HepG2	liver:	n/a	chr4:133246262-133246273 chr4:133246273-133246286 chr4:133246273-133246284
19	CEBPB	chr4:133240156-133240388	A549	lung:	n/a	chr4:133240209-133240220 chr4:133240188-133240199 chr4:133240209-133240222
20	CEBPB	chr4:133228262-133228577	IMR90	lung:	n/a	chr4:133228409-133228420
21	CEBPB	chr4:133234391-133234624	IMR90	lung:	n/a	n/a
22	CEBPB	chr4:133223604-133223874	HepG2	liver:	n/a	chr4:133223742-133223753 chr4:133223743-133223754 chr4:133223742-133223755
23	CEBPB	chr4:133223702-133223847	H1-hESC	embryonic stem cell:	n/a	chr4:133223742-133223753 chr4:133223743-133223754 chr4:133223742-133223755
24	CEBPB	chr4:133234378-133234608	A549	lung:	n/a	n/a
25	CEBPB	chr4:133240074-133240372	K562	blood:	n/a	chr4:133240209-133240220 chr4:133240188-133240199 chr4:133240209-133240222
26	CHD2	chr4:133266055-133266671	K562	blood:	n/a	n/a
27	CHD2	chr4:133265720-133266696	Hela-S3	cervix:	n/a	n/a
28	CTCF	chr4:133289520-133289670	WERI-Rb-1	eye:	n/a	n/a
29	CTCF	chr4:133254260-133254410	BE2_C	brain:	n/a	chr4:133254290-133254299
30	CTCF	chr4:133254080-133254230	A549	lung:	n/a	n/a
31	CTCF	chr4:133254180-133254330	HCFaa	heart:	n/a	chr4:133254290-133254299
32	CTCF	chr4:133253840-133253990	BE2_C	brain:	n/a	n/a
33	CTCF	chr4:133254420-133254570	BJ	skin:	n/a	n/a
34	CTCF	chr4:133254200-133254350	AG04449	skin:	n/a	chr4:133254290-133254299
35	CTCF	chr4:133254180-133254330	HAc	cerebellar:	n/a	chr4:133254290-133254299
36	CTCF	chr4:133254104-133254450	GM12878	blood:	n/a	chr4:133254290-133254299
37	CTCF	chr4:133287320-133287470	GM12866	blood:	n/a	n/a
38	CTCF	chr4:133254154-133254401	Medullo	brain:	n/a	chr4:133254290-133254299
39	CTCF	chr4:133254176-133254416	LNCaP	prostate:	n/a	chr4:133254290-133254299
40	CTCF	chr4:133254111-133254502	HCT-116	colon:	n/a	chr4:133254290-133254299
41	CTCF	chr4:133254220-133254370	HCT-116	colon:	n/a	chr4:133254290-133254299
42	CTCF	chr4:133254235-133254351	GM10248	blood:	n/a	chr4:133254290-133254299
43	CTCF	chr4:133254300-133254450	A549	lung:	n/a	n/a
44	CTCF	chr4:133254240-133254390	HCT-116	colon:	n/a	chr4:133254290-133254299
45	CTCF	chr4:133253952-133254048	HUVEC	blood vessel:	n/a	n/a
46	CTCF	chr4:133254147-133254421	HUVEC	blood vessel:	n/a	chr4:133254290-133254299
47	CTCF	chr4:133254260-133254410	Hela-S3	cervix:	n/a	chr4:133254290-133254299
48	CTCF	chr4:133254200-133254350	AoAF	blood vessel:	n/a	chr4:133254290-133254299
49	CTCF	chr4:133254199-133254333	SK-N-SH_RA	brain:	n/a	chr4:133254290-133254299
50	CTCF	chr4:133254180-133254330	A549	lung:	n/a	chr4:133254290-133254299

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:133266193-133266243	GM12892	blood:	n/a
2	chr4:133266193-133266243	GM19239	blood:	n/a
3	chr4:133266193-133266243	PrEC	prostate:	n/a
4	chr4:133266322-133266372	HPAEpiC	pulmonary alveolar:	n/a
5	chr4:133266193-133266243	PFSK-1	brain:	n/a
6	chr4:133266193-133266243	HCF	heart:	n/a
7	chr4:133266322-133266372	GM12878	blood:	n/a
8	chr4:133266193-133266243	T-47D	breast:	n/a
9	chr4:133266322-133266372	ProgFib	skin:	n/a
10	chr4:133266322-133266372	HAEpiC	amniotic membrane:	n/a
11	chr4:133266322-133266372	HRE	kidney:	n/a
12	chr4:133266322-133266372	NH-A	brain:	n/a
13	chr4:133266322-133266372	GM12892	blood:	n/a
14	chr4:133266193-133266243	AG10803	skin:	n/a
15	chr4:133266193-133266243	ECC-1	luminal epithelium:	n/a
16	chr4:133266193-133266243	Hela-S3	cervix:	n/a
17	chr4:133266322-133266372	LNCaP	prostate:	n/a
18	chr4:133266193-133266243	U87	brain:	n/a
19	chr4:133266193-133266243	HIPEpiC	eye:	n/a
20	chr4:133266322-133266372	PrEC	prostate:	n/a
21	chr4:133266193-133266243	NHDF-neo	bronchial:	n/a
22	chr4:133266193-133266243	GM12891	blood:	n/a
23	chr4:133266322-133266372	SK-N-MC	brain:	n/a
24	chr4:133266322-133266372	HMEC	breast:	n/a
25	chr4:133266322-133266372	GM19239	blood:	n/a
26	chr4:133266322-133266372	CMK	blood:	n/a
27	chr4:133266193-133266243	HMEC	breast:	n/a
28	chr4:133266193-133266243	HUVEC	blood vessel:	n/a
29	chr4:133266193-133266243	HRCEpiC	kidney:	n/a
30	chr4:133266193-133266243	SKMC	muscle:	n/a
31	chr4:133266322-133266372	ECC-1	luminal epithelium:	n/a
32	chr4:133266193-133266243	SK-N-SH_RA	brain:	n/a
33	chr4:133266322-133266372	SK-N-SH_RA	brain:	n/a
34	chr4:133266193-133266243	CMK	blood:	n/a
35	chr4:133266322-133266372	AG04449	skin:	fetal
36	chr4:133266322-133266372	AG04450	lung:	fetal
37	chr4:133266322-133266372	GM06990	blood:	n/a
38	chr4:133266193-133266243	AG09309	skin:	n/a
39	chr4:133266193-133266243	A549	lung:	n/a
40	chr4:133266322-133266372	ovcar-3	ovarian:	n/a
41	chr4:133266193-133266243	NHBE	bronchial:	n/a
42	chr4:133266322-133266372	Hepatocyte	liver:	n/a
43	chr4:133266322-133266372	AG09319	gingival:	n/a
44	chr4:133266322-133266372	U87	brain:	n/a
45	chr4:133266193-133266243	Caco-2	colon:	n/a
46	chr4:133266193-133266243	HNPCEpiC	eye:	n/a
47	chr4:133266322-133266372	T-47D	breast:	n/a
48	chr4:133266193-133266243	HRE	kidney:	n/a
49	chr4:133266322-133266372	HEK293	kidney:	embryo
50	chr4:133266193-133266243	RPTEC	kidney:	n/a

No.	Distal block	Cell Line	Cell type
1	chr4:133264521..133268108-chr4:133268991..133272057,6	K562	blood:
2	chr4:133246638..133249812-chr4:133265864..133268563,3	K562	blood:
3	chr4:133264521..133268108-chr4:133268991..133272057,6	K562	blood:
4	chr4:133263144..133265552-chr4:133295032..133296835,2	K562	blood:
5	chr4:133265507..133268108-chr4:133268991..133271558,3	K562	blood:
6	chr4:133254539..133258188-chr4:133265340..133266888,3	K562	blood:
7	chr4:133246638..133249812-chr4:133265864..133268563,3	K562	blood:
8	chr4:133265507..133268108-chr4:133268991..133271558,3	K562	blood:
9	chr4:133254539..133258188-chr4:133265340..133266888,3	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RP11-62N21.1.1-11	chr4:133288941-133289634	NONHSAT098333

Variant related genes	Relation type
ELL2P2	TF binding region
ELL2P2	CpG island

Extended variants
information (count: 1809 )
Associated
traits (count: 76 )

Variant overlapped rSNPs/rCNVs (count:1809 , 50 per page) page: 1 2 3 4 5 6 7 ... 37

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs9997674	chr4:133160255-133160256	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs189614027	chr4:133160269-133160270	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs147461454	chr4:133160270-133160271	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs529690914	chr4:133160276-133160277	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs565723691	chr4:133160288-133160289	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs374044715	chr4:133160337-133160338	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs9997695	chr4:133160380-133160381	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs538845743	chr4:133160396-133160397	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs139841561	chr4:133160397-133160398	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs569271412	chr4:133160413-133160414	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs181944135	chr4:133160454-133160455	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs554748981	chr4:133160495-133160496	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs574825756	chr4:133160507-133160508	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs533925766	chr4:133160516-133160517	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs145457907	chr4:133160520-133160521	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs577078815	chr4:133160571-133160572	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs184722330	chr4:133160630-133160631	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs150638504	chr4:133160637-133160638	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs576545490	chr4:133160640-133160641	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs188829041	chr4:133160641-133160642	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs560815866	chr4:133160653-133160654	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs529756092	chr4:133160668-133160669	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs368241528	chr4:133160683-133160684	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs139930155	chr4:133160705-133160706	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs1499324	chr4:133160737-133160738	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs181591989	chr4:133160769-133160770	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs186004096	chr4:133160782-133160783	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs531405517	chr4:133160786-133160787	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs548705318	chr4:133160805-133160806	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs568178628	chr4:133160810-133160811	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs1499323	chr4:133160840-133160841	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs1499322	chr4:133160849-133160850	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs570825740	chr4:133160871-133160872	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs540161378	chr4:133160901-133160902	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs556559495	chr4:133160907-133160908	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs576623032	chr4:133160929-133160930	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs542046912	chr4:133161004-133161005	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs554658730	chr4:133161015-133161016	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs574538068	chr4:133161101-133161102	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs370199276	chr4:133161130-133161131	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs540251817	chr4:133161132-133161133	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs560153393	chr4:133161167-133161168	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs374445175	chr4:133161251-133161252	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs532128557	chr4:133161276-133161277	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs149818963	chr4:133161327-133161328	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs368609679	chr4:133161330-133161331	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs531543900	chr4:133161354-133161355	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs28493696	chr4:133161361-133161362	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs145882766	chr4:133161396-133161397	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs189487794	chr4:133161457-133161458	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:76)

Disease	PMID	Source
Acute lymphoblastic leukemia	22237106	CNVD
Glioblastoma multiforme	21080181	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Chordoma	21602918	CNVD
HIV/AIDS	22032296	CNVD
Medulloblastoma	21979893	CNVD
Neuroblastoma	18923191	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	21858162	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Gastric cancer	21586687	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Breast cancer	16272173	CNVD
Colorectal cancer	19359472	CNVD
Malignant mesothelioma	18160781	CNVD
Medulloblastoma	18056178	CNVD
Multiple myeloma	17077331	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Oral squamous cell carcinoma	17134496	CNVD
4q-syndrome	17576883	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Colorectal cancer	20709793	CNVD
Muscular dystrophy	21149563	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Cervical cancer	21062161	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	16608533	CNVD
Lung cancer	19208797	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	21785460	CNVD
Lung cancer	18438408	CNVD
Cancer	22429812	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	21183584	CNVD
primary effusion lymphomas	17116491	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17133270	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Congenital anomalies of the kidney and urinary tract	20505237	CNVD
Breast cancer	17393978	CNVD
Esophageal cancer	21851588	CNVD
Colorectal cancer	16272173	CNVD
Testicular germ cell tumor	18059402	CNVD
Ovarian cancer	22174824	CNVD
Neuroblastoma	21899760	CNVD
Renal cell carcinoma	18194544	CNVD
Olfactory neuroblastoma	18408657	CNVD
Hepatocellular carcinoma	16750200	CNVD
Acute myeloid leukemia	16864856	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Hodgkin''s lymphoma	17606441	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Colorectal cancer	20459617	CNVD
Lung squamous cell carcinoma	22363434	CNVD
Mental retardation	17847001	CNVD
Myelofibrosis	22110671	CNVD
Autism	18923514	CNVD
Autism	22241247	CNVD
Mental retardation	17901693	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
small cell lung cancer	20016488	CNVD

Chromatin state (count:92 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:133159400-133160400	Enhancers	Stomach Mucosa	stomach
2	chr4:133159800-133160400	Enhancers	Fetal Intestine Large	intestine
3	chr4:133159800-133161600	Enhancers	Fetal Intestine Small	intestine
4	chr4:133160000-133160600	Enhancers	Duodenum Mucosa	Duodenum
5	chr4:133160000-133160600	Enhancers	Gastric	stomach
6	chr4:133160400-133161400	Weak transcription	Fetal Intestine Large	intestine
7	chr4:133160400-133165600	Weak transcription	Stomach Mucosa	stomach
8	chr4:133160600-133165000	Weak transcription	Duodenum Mucosa	Duodenum
9	chr4:133160800-133161600	Enhancers	HUVEC	blood vessel
10	chr4:133161200-133161600	Enhancers	Dnd41	blood
11	chr4:133161400-133161600	Enhancers	Fetal Intestine Large	intestine
12	chr4:133161600-133165600	Weak transcription	Fetal Intestine Small	intestine
13	chr4:133165400-133167000	Enhancers	Pancreatic Islets	Pancreatic Islet
14	chr4:133165600-133166200	Enhancers	Stomach Mucosa	stomach
15	chr4:133165600-133167000	Enhancers	Fetal Intestine Small	intestine
16	chr4:133165800-133167000	Enhancers	Fetal Lung	lung
17	chr4:133166600-133166800	Enhancers	Duodenum Mucosa	Duodenum
18	chr4:133167000-133169600	Weak transcription	Fetal Intestine Small	intestine
19	chr4:133183000-133184800	Weak transcription	Fetal Thymus	thymus
20	chr4:133184000-133190000	Enhancers	Dnd41	blood
21	chr4:133184800-133185600	Enhancers	Fetal Lung	lung
22	chr4:133184800-133185600	Enhancers	Fetal Thymus	thymus
23	chr4:133185000-133185600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
24	chr4:133185600-133187600	Weak transcription	Fetal Lung	lung
25	chr4:133185600-133187800	Weak transcription	Fetal Thymus	thymus
26	chr4:133187400-133188600	Enhancers	Primary T cells from cord blood	blood
27	chr4:133187600-133188000	Enhancers	Fetal Lung	lung
28	chr4:133187600-133188400	Enhancers	Primary B cells from cord blood	blood
29	chr4:133187800-133188600	Enhancers	Fetal Thymus	thymus
30	chr4:133188200-133188800	Enhancers	Thymus	Thymus
31	chr4:133188600-133190000	Weak transcription	Fetal Thymus	thymus
32	chr4:133190000-133190400	Weak transcription	Dnd41	blood
33	chr4:133190000-133190800	ZNF genes & repeats	Fetal Thymus	thymus
34	chr4:133190400-133191000	ZNF genes & repeats	Dnd41	blood
35	chr4:133190600-133190800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
36	chr4:133190600-133191000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
37	chr4:133200000-133200400	Weak transcription	H9 Cell Line	embryonic stem cell
38	chr4:133201200-133201600	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
39	chr4:133201600-133205600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
40	chr4:133204200-133204600	Enhancers	HUES48 Cell Line	embryonic stem cell
41	chr4:133204200-133204600	Enhancers	iPS-15b Cell Line	embryonic stem cell
42	chr4:133204600-133205800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
43	chr4:133205600-133206400	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
44	chr4:133205600-133207400	ZNF genes & repeats	Dnd41	blood
45	chr4:133205800-133206000	ZNF genes & repeats	iPS-15b Cell Line	embryonic stem cell
46	chr4:133205800-133206200	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
47	chr4:133217600-133218200	Active TSS	Primary B cells from cord blood	blood
48	chr4:133217600-133219200	Enhancers	Fetal Lung	lung
49	chr4:133217800-133218200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
50	chr4:133218200-133218800	Weak transcription	Primary B cells from cord blood	blood

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