Variant report

Variant	nsv881472
Chromosome Location	chr4:187152142-187187005
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	chr4:187186808-187187453	HepG2	liver:	n/a	n/a
2	ARID3A	chr4:187171041-187171245	HepG2	liver:	n/a	n/a
3	ARID3A	chr4:187181380-187182509	HepG2	liver:	n/a	n/a
4	ATF2	chr4:187161672-187163517	H1-hESC	embryonic stem cell:	n/a	n/a
5	ATF2	chr4:187169713-187170235	H1-hESC	embryonic stem cell:	n/a	n/a
6	ATF2	chr4:187164423-187164838	H1-hESC	embryonic stem cell:	n/a	n/a
7	ATF2	chr4:187165329-187165708	H1-hESC	embryonic stem cell:	n/a	n/a
8	ATF2	chr4:187165144-187167561	H1-hESC	embryonic stem cell:	n/a	n/a
9	ATF2	chr4:187168595-187169103	H1-hESC	embryonic stem cell:	n/a	n/a
10	ATF2	chr4:187167865-187168978	H1-hESC	embryonic stem cell:	n/a	n/a
11	ATF2	chr4:187167786-187168560	H1-hESC	embryonic stem cell:	n/a	n/a
12	ATF2	chr4:187169367-187170182	H1-hESC	embryonic stem cell:	n/a	n/a
13	ATF2	chr4:187161516-187163596	H1-hESC	embryonic stem cell:	n/a	n/a
14	ATF2	chr4:187171045-187171934	H1-hESC	embryonic stem cell:	n/a	n/a
15	ATF2	chr4:187171143-187171925	H1-hESC	embryonic stem cell:	n/a	n/a
16	ATF2	chr4:187164166-187164972	H1-hESC	embryonic stem cell:	n/a	n/a
17	BACH1	chr4:187171005-187171725	H1-hESC	embryonic stem cell:	n/a	n/a
18	BACH1	chr4:187169575-187170178	H1-hESC	embryonic stem cell:	n/a	n/a
19	BCL11A	chr4:187169816-187170171	H1-hESC	embryonic stem cell:	n/a	n/a
20	BCL11A	chr4:187161578-187162735	H1-hESC	embryonic stem cell:	n/a	chr4:187162412-187162421 chr4:187161895-187161904
21	BHLHE40	chr4:187181692-187182406	HepG2	liver:	n/a	n/a
22	BRCA1	chr4:187171414-187171895	H1-hESC	embryonic stem cell:	n/a	n/a
23	CEBPB	chr4:187156190-187156343	H1-hESC	embryonic stem cell:	n/a	n/a
24	CEBPB	chr4:187171067-187171771	H1-hESC	embryonic stem cell:	n/a	chr4:187171133-187171144
25	CEBPB	chr4:187168912-187169588	H1-hESC	embryonic stem cell:	n/a	n/a
26	CEBPB	chr4:187181610-187182115	HepG2	liver:	n/a	chr4:187181863-187181874 chr4:187181884-187181895 chr4:187181883-187181896
27	CEBPB	chr4:187181710-187181921	HepG2	liver:	n/a	chr4:187181863-187181874 chr4:187181884-187181895 chr4:187181883-187181896
28	CEBPB	chr4:187172930-187173153	H1-hESC	embryonic stem cell:	n/a	n/a
29	CEBPB	chr4:187152903-187153108	HepG2	liver:	n/a	chr4:187153043-187153052 chr4:187153043-187153052 chr4:187153041-187153052 chr4:187153043-187153052 chr4:187153041-187153054 chr4:187153042-187153053 chr4:187153043-187153052
30	CEBPB	chr4:187152993-187153115	IMR90	lung:	n/a	chr4:187153043-187153052 chr4:187153043-187153052 chr4:187153041-187153052 chr4:187153043-187153052 chr4:187153041-187153054 chr4:187153042-187153053 chr4:187153043-187153052
31	CEBPB	chr4:187171043-187171232	A549	lung:	n/a	chr4:187171133-187171144
32	CEBPB	chr4:187179489-187179743	A549	lung:	n/a	chr4:187179598-187179609
33	CEBPB	chr4:187172830-187173086	A549	lung:	n/a	n/a
34	CEBPB	chr4:187186894-187187383	HepG2	liver:	n/a	n/a
35	CEBPB	chr4:187153022-187153058	A549	lung:	n/a	chr4:187153043-187153052 chr4:187153043-187153052 chr4:187153041-187153052 chr4:187153043-187153052 chr4:187153041-187153054 chr4:187153042-187153053 chr4:187153043-187153052
36	CEBPB	chr4:187170950-187171465	IMR90	lung:	n/a	chr4:187171133-187171144
37	CEBPB	chr4:187179425-187179787	HepG2	liver:	n/a	chr4:187179598-187179609
38	CEBPB	chr4:187175483-187175554	HepG2	liver:	n/a	chr4:187175512-187175523
39	CEBPB	chr4:187172826-187173166	HepG2	liver:	n/a	n/a
40	CEBPB	chr4:187152925-187153145	K562	blood:	n/a	chr4:187153043-187153052 chr4:187153043-187153052 chr4:187153041-187153052 chr4:187153043-187153052 chr4:187153041-187153054 chr4:187153042-187153053 chr4:187153043-187153052
41	CEBPB	chr4:187181738-187182008	IMR90	lung:	n/a	chr4:187181863-187181874 chr4:187181884-187181895 chr4:187181883-187181896
42	CEBPB	chr4:187172843-187173128	IMR90	lung:	n/a	n/a
43	CEBPB	chr4:187169039-187169120	A549	lung:	n/a	n/a
44	CEBPB	chr4:187157320-187157520	HepG2	liver:	n/a	n/a
45	CEBPB	chr4:187172954-187173126	K562	blood:	n/a	n/a
46	CHD1	chr4:187171070-187171475	H1-hESC	embryonic stem cell:	n/a	n/a
47	CHD1	chr4:187164273-187164920	H1-hESC	embryonic stem cell:	n/a	n/a
48	CHD1	chr4:187161706-187163174	H1-hESC	embryonic stem cell:	n/a	n/a
49	CHD1	chr4:187171682-187172114	H1-hESC	embryonic stem cell:	n/a	n/a
50	CHD1	chr4:187165142-187170727	H1-hESC	embryonic stem cell:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:187185716-187185766	HUVEC	blood vessel:	n/a
2	chr4:187185997-187186047	HCM	heart:	n/a
3	chr4:187185716-187185766	U87	brain:	n/a
4	chr4:187185716-187185766	NHDF-neo	bronchial:	n/a
5	chr4:187186265-187186315	HCPEpiC	choroid plexus:	n/a
6	chr4:187185716-187185766	Caco-2	colon:	n/a
7	chr4:187186953-187187003	NHDF-neo	bronchial:	n/a
8	chr4:187185716-187185766	SK-N-MC	brain:	n/a
9	chr4:187162262-187162312	HRCEpiC	kidney:	n/a
10	chr4:187185997-187186047	MCF-7	breast:	n/a
11	chr4:187186953-187187003	Hepatocyte	liver:	n/a
12	chr4:187186265-187186315	SAEC	small airway:	n/a
13	chr4:187186953-187187003	CMK	blood:	n/a
14	chr4:187185997-187186047	BJ	skin:	n/a
15	chr4:187186949-187186999	SAEC	small airway:	n/a
16	chr4:187185716-187185766	AG09319	gingival:	n/a
17	chr4:187181470-187181520	AG10803	skin:	n/a
18	chr4:187186953-187187003	NB4	blood:	n/a
19	chr4:187186265-187186315	PANC-1	pancreas:	n/a
20	chr4:187186265-187186315	GM19239	blood:	n/a
21	chr4:187181470-187181520	HNPCEpiC	eye:	n/a
22	chr4:187162262-187162312	HepG2	liver:	n/a
23	chr4:187162262-187162312	HEEpiC	esophagus:	n/a
24	chr4:187162262-187162312	AG09319	gingival:	n/a
25	chr4:187162262-187162312	HRE	kidney:	n/a
26	chr4:187185997-187186047	NHDF-neo	bronchial:	n/a
27	chr4:187181470-187181520	HPAEpiC	pulmonary alveolar:	n/a
28	chr4:187185997-187186047	GM12878	blood:	n/a
29	chr4:187181470-187181520	NT2-D1	testis:	n/a
30	chr4:187181470-187181520	RPTEC	kidney:	n/a
31	chr4:187186949-187186999	HMEC	breast:	n/a
32	chr4:187186949-187186999	BE2_C	brain:	n/a
33	chr4:187185716-187185766	Jurkat	blood:	n/a
34	chr4:187181470-187181520	ECC-1	luminal epithelium:	n/a
35	chr4:187186953-187187003	ovcar-3	ovarian:	n/a
36	chr4:187186953-187187003	HEEpiC	esophagus:	n/a
37	chr4:187186949-187186999	IMR90	lung:	fetal
38	chr4:187186949-187186999	GM12892	blood:	n/a
39	chr4:187181470-187181520	AG04449	skin:	fetal
40	chr4:187186953-187187003	GM12878	blood:	n/a
41	chr4:187162262-187162312	AG04449	skin:	fetal
42	chr4:187186265-187186315	HEEpiC	esophagus:	n/a
43	chr4:187186949-187186999	AoSMC	blood vessel:	n/a
44	chr4:187181470-187181520	SAEC	small airway:	n/a
45	chr4:187185997-187186047	SAEC	small airway:	n/a
46	chr4:187162262-187162312	HCPEpiC	choroid plexus:	n/a
47	chr4:187186265-187186315	BE2_C	brain:	n/a
48	chr4:187185997-187186047	NHBE	bronchial:	n/a
49	chr4:187181470-187181520	AoSMC	blood vessel:	n/a
50	chr4:187186265-187186315	NHBE	bronchial:	n/a

No.	Distal block	Cell Line	Cell type
1	chr4:187150164..187152191-chr4:187152887..187155596,2	K562	blood:
2	chr4:187150164..187152191-chr4:187152887..187155596,2	K562	blood:
3	chr4:187111874..187113781-chr4:187171263..187172793,2	MCF-7	breast:
4	chr4:187143055..187145709-chr4:187150430..187152573,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-F11-6	chr4:187173827-187173894	l_2815_chr4:187173826-187177044_heart
2	lnc-F11-6	chr4:187176601-187177044	l_2815_chr4:187173826-187177044_heart
3	lnc-F11-6	chr4:187175427-187175535	l_2815_chr4:187173826-187177044_heart

Variant related genes	Relation type
F11	TF binding region
KLKB1	TF binding region
F11	CpG island
KLKB1	CpG island
ENSG00000269302	chromatin interactions
ENSG00000145476	chromatin interactions

Extended variants
information (count: 1659 )
Associated
traits (count: 77 )

Variant overlapped rSNPs/rCNVs (count:1659 , 50 per page) page: 1 2 3 4 5 6 7 ... 34

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4241815	chr4:187152142-187152143	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs571909436	chr4:187152175-187152176	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs372623461	chr4:187152212-187152213	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs111601919	chr4:187152238-187152239	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs577813935	chr4:187152240-187152241	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs35425601	chr4:187152254-187152255	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs545238513	chr4:187152276-187152277	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs564625180	chr4:187152289-187152290	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs376885789	chr4:187152307-187152308	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs4241816	chr4:187152327-187152328	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	disease
11	rs563471357	chr4:187152356-187152357	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs115136459	chr4:187152359-187152360	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs4253337	chr4:187152368-187152369	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs566068194	chr4:187152386-187152387	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs528473375	chr4:187152420-187152421	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs547710196	chr4:187152482-187152483	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs188532305	chr4:187152484-187152485	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs150427307	chr4:187152490-187152491	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs28659787	chr4:187152548-187152549	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs149080348	chr4:187152552-187152553	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs34058869	chr4:187152567-187152568	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs374630623	chr4:187152621-187152622	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs4241817	chr4:187152658-187152659	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs193164085	chr4:187152676-187152677	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs561730597	chr4:187152712-187152713	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs79290868	chr4:187152718-187152719	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs572056415	chr4:187152720-187152721	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs534313561	chr4:187152768-187152769	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs558464611	chr4:187152884-187152885	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs578172479	chr4:187152899-187152900	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs543681085	chr4:187152916-187152917	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs528931591	chr4:187152928-187152929	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs563548109	chr4:187153022-187153023	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs544290141	chr4:187153025-187153026	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs35389013	chr4:187153068-187153069	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs573848787	chr4:187153099-187153100	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs562611827	chr4:187153204-187153205	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs370086908	chr4:187153239-187153240	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs533148132	chr4:187153242-187153243	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs542759899	chr4:187153251-187153252	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs369438768	chr4:187153252-187153253	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs148277206	chr4:187153290-187153291	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs138408657	chr4:187153327-187153328	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs576466131	chr4:187153328-187153329	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs528518519	chr4:187153357-187153358	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs374181790	chr4:187153393-187153394	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs142462112	chr4:187153432-187153433	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs114817536	chr4:187153453-187153454	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs201749287	chr4:187153461-187153462	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs369855039	chr4:187153463-187153464	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:77)

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
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
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
Wilms tumour	21544195	CNVD
Lung cancer	18438408	CNVD
Cancer	22429812	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Breast cancer	16272173	CNVD
Breast cancer	17133270	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Congenital anomalies of the kidney and urinary tract	20505237	CNVD
Testicular germ cell tumor	18059402	CNVD
Ovarian cancer	22174824	CNVD
Olfactory neuroblastoma	18408657	CNVD
Breast cancer	21785460	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Hodgkin''s lymphoma	17606441	CNVD
small cell lung cancer	20016488	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Ewing''s sarcoma	17952124	CNVD
Breast cancer	21633010	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Cancer	20581869	CNVD
Hepatocellular carcinoma	16750200	CNVD
abnormal development	18461090	CNVD
Neuroblastoma	16790693	CNVD
Colorectal cancer	16774939	CNVD
Congenital anomalies of the kidney and urinary tract	18316590	CNVD
Basal cell lymphoma	17053054	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Myelofibrosis	22110671	CNVD
Lung adenocarcinoma	17086460	CNVD
Facioscapulohumeral muscular dystrophy	21829175	CNVD
Disorders of sex development	21048976	CNVD
Ovarian cancer	20844748	CNVD
Autism	18414403	CNVD
Urothelial carcinoma	21177765	CNVD
Cancer	20164920	CNVD
Cancer	20164919	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	20409316	CNVD
Rhabdomyosarcoma	16790082	CNVD
Prostate cancer	22341455	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:420 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:187131800-187159000	Weak transcription	Skeletal Muscle Male	skeletal muscle
2	chr4:187131800-187181600	Weak transcription	Brain Hippocampus Middle	brain
3	chr4:187146400-187172800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
4	chr4:187147800-187162000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
5	chr4:187148000-187161600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
6	chr4:187148000-187173000	Weak transcription	Psoas Muscle	Psoas
7	chr4:187148200-187159400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
8	chr4:187148200-187179200	Weak transcription	Lung	lung
9	chr4:187148400-187162000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
10	chr4:187148400-187164600	Weak transcription	Right Ventricle	heart
11	chr4:187148400-187172600	Weak transcription	Brain Anterior Caudate	brain
12	chr4:187148400-187179400	Weak transcription	Pancreas	Pancrea
13	chr4:187149600-187159400	Weak transcription	Fetal Intestine Small	intestine
14	chr4:187149800-187181600	Weak transcription	Duodenum Mucosa	Duodenum
15	chr4:187149800-187186800	Weak transcription	Rectal Mucosa Donor 31	rectum
16	chr4:187150000-187161000	Weak transcription	Aorta	Aorta
17	chr4:187150000-187162000	Weak transcription	HUES48 Cell Line	embryonic stem cell
18	chr4:187150200-187187200	Weak transcription	Duodenum Smooth Muscle	Duodenum
19	chr4:187151000-187187200	Weak transcription	Colon Smooth Muscle	Colon
20	chr4:187151200-187153000	Enhancers	Liver	Liver
21	chr4:187151200-187161200	Weak transcription	Pancreatic Islets	Pancreatic Islet
22	chr4:187151800-187173000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
23	chr4:187152000-187179400	Weak transcription	Brain Inferior Temporal Lobe	brain
24	chr4:187152200-187169800	Weak transcription	Brain Substantia Nigra	brain
25	chr4:187153000-187156800	Genic enhancers	Liver	Liver
26	chr4:187154000-187182000	Weak transcription	Primary T cells from cord blood	blood
27	chr4:187156600-187156800	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
28	chr4:187156800-187158200	Enhancers	Liver	Liver
29	chr4:187156800-187179200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
30	chr4:187158000-187173000	Weak transcription	Left Ventricle	heart
31	chr4:187158200-187158600	Weak transcription	Liver	Liver
32	chr4:187158400-187181400	Weak transcription	Fetal Intestine Large	intestine
33	chr4:187158600-187160200	Strong transcription	Liver	Liver
34	chr4:187159000-187159800	Enhancers	iPS-18 Cell Line	embryonic stem cell
35	chr4:187159000-187159800	Strong transcription	Skeletal Muscle Male	skeletal muscle
36	chr4:187159400-187159600	ZNF genes & repeats	iPS DF 6.9 Cell Line	embryonic stem cell
37	chr4:187159400-187159800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
38	chr4:187159400-187159800	ZNF genes & repeats	Fetal Intestine Small	intestine
39	chr4:187159400-187160000	ZNF genes & repeats	Breast Myoepithelial Primary Cells	Breast
40	chr4:187159600-187162000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
41	chr4:187159800-187161800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
42	chr4:187159800-187161800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
43	chr4:187159800-187164800	Weak transcription	Fetal Intestine Small	intestine
44	chr4:187159800-187172600	Weak transcription	Skeletal Muscle Male	skeletal muscle
45	chr4:187160000-187160200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
46	chr4:187160200-187161000	Weak transcription	Liver	Liver
47	chr4:187161000-187165200	Strong transcription	Liver	Liver
48	chr4:187161200-187162600	Enhancers	Pancreatic Islets	Pancreatic Islet
49	chr4:187161600-187162600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
50	chr4:187161800-187162200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell

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