Variant report

Variant	nsv879492
Chromosome Location	chr4:76088845-76154064
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:172)
CpG islands
(count:62)
Chromatin interactive
region (count:2)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:172 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr4:76097665-76098276	GM12878	blood:	n/a	n/a
2	ATF2	chr4:76097733-76098242	GM12878	blood:	n/a	n/a
3	BATF	chr4:76097783-76098119	GM12878	blood:	n/a	chr4:76097965-76097976
4	BATF	chr4:76097808-76098155	GM12878	blood:	n/a	chr4:76097965-76097976
5	BCL11A	chr4:76097809-76098050	GM12878	blood:	n/a	n/a
6	BCL3	chr4:76097780-76098198	GM12878	blood:	n/a	n/a
7	BCLAF1	chr4:76097714-76098283	GM12878	blood:	n/a	n/a
8	BHLHE40	chr4:76097826-76098078	GM12878	blood:	n/a	n/a
9	BRCA1	chr4:76106466-76106496	GM12878	blood:	n/a	n/a
10	CEBPB	chr4:76115753-76115953	HepG2	liver:	n/a	chr4:76115809-76115820
11	CHD2	chr4:76106489-76106715	GM12878	blood:	n/a	n/a
12	CREB1	chr4:76097705-76098333	GM12878	blood:	n/a	n/a
13	CTCF	chr4:76106464-76106549	H1-hESC	embryonic stem cell:	n/a	n/a
14	CTCF	chr4:76106840-76106990	GM12875	blood:	n/a	n/a
15	CTCF	chr4:76106440-76106590	HepG2	liver:	n/a	n/a
16	CTCF	chr4:76106480-76106630	GM12870	blood:	n/a	n/a
17	CTCF	chr4:76106540-76106690	GM12867	blood:	n/a	n/a
18	CTCF	chr4:76106440-76106590	GM06990	blood:	n/a	n/a
19	CTCF	chr4:76118940-76119090	GM12866	blood:	n/a	n/a
20	CTCF	chr4:76106160-76106310	GM06990	blood:	n/a	n/a
21	CTCF	chr4:76106560-76106710	GM12874	blood:	n/a	n/a
22	CTCF	chr4:76106840-76106990	GM12873	blood:	n/a	n/a
23	CTCF	chr4:76106340-76106490	GM12873	blood:	n/a	n/a
24	CTCF	chr4:76106480-76106630	GM12871	blood:	n/a	n/a
25	CTCF	chr4:76108810-76108873	GM20000	blood:	n/a	n/a
26	CTCF	chr4:76106620-76106770	GM12864	blood:	n/a	n/a
27	CTCF	chr4:76151314-76151358	LNCaP	prostate:	n/a	n/a
28	CTCF	chr4:76135760-76135910	GM12865	blood:	n/a	n/a
29	CTCF	chr4:76106240-76106390	GM12870	blood:	n/a	n/a
30	CTCF	chr4:76108243-76108287	GM13977	blood:	n/a	n/a
31	CTCF	chr4:76106240-76106390	GM12868	blood:	n/a	n/a
32	CTCF	chr4:76106520-76106670	GM12865	blood:	n/a	n/a
33	CTCF	chr4:76106460-76106610	GM12864	blood:	n/a	n/a
34	CTCF	chr4:76106240-76106390	GM12864	blood:	n/a	n/a
35	CTCF	chr4:76106540-76106690	GM12868	blood:	n/a	n/a
36	CTCF	chr4:76101639-76101698	GM13976	blood:	n/a	n/a
37	CTCF	chr4:76106440-76106590	GM12872	blood:	n/a	n/a
38	CUX1	chr4:76131561-76131571	GM12878	blood:	n/a	n/a
39	CUX1	chr4:76097844-76098229	GM12878	blood:	n/a	n/a
40	EBF1	chr4:76106065-76106855	GM12878	blood:	n/a	chr4:76106479-76106490
41	EBF1	chr4:76106268-76106670	GM12878	blood:	n/a	chr4:76106479-76106490
42	EBF1	chr4:76097736-76098390	GM12878	blood:	n/a	n/a
43	EBF1	chr4:76106206-76106939	GM12878	blood:	n/a	chr4:76106479-76106490
44	EBF1	chr4:76097814-76098091	GM12878	blood:	n/a	n/a
45	EGR1	chr4:76106358-76106805	HCT-116	colon:	n/a	n/a
46	EGR1	chr4:76106404-76106710	K562	blood:	n/a	n/a
47	EGR1	chr4:76106224-76106798	HCT-116	colon:	n/a	n/a
48	EGR1	chr4:76106360-76106705	K562	blood:	n/a	n/a
49	EP300	chr4:76094400-76095203	ECC-1	luminal epithelium:	n/a	n/a
50	EP300	chr4:76106408-76106603	GM12878	blood:	n/a	n/a

(count:62 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:76094406-76094456	PrEC	prostate:	n/a
2	chr4:76094406-76094456	PrEC	prostate:	n/a
3	chr4:76094406-76094456	GM12892	blood:	n/a
4	chr4:76094406-76094456	AG10803	skin:	n/a
5	chr4:76094406-76094456	HEK293	kidney:	embryo
6	chr4:76094406-76094456	ovcar-3	ovarian:	n/a
7	chr4:76094406-76094456	HNPCEpiC	eye:	n/a
8	chr4:76094406-76094456	A549	lung:	n/a
9	chr4:76094406-76094456	SK-N-SH	brain:	n/a
10	chr4:76094406-76094456	PANC-1	pancreas:	n/a
11	chr4:76094406-76094456	SK-N-MC	brain:	n/a
12	chr4:76094406-76094456	HEEpiC	esophagus:	n/a
13	chr4:76094406-76094456	MCF-7	breast:	n/a
14	chr4:76094406-76094456	AG09309	skin:	n/a
15	chr4:76094406-76094456	AG09319	gingival:	n/a
16	chr4:76094406-76094456	SAEC	small airway:	n/a
17	chr4:76094406-76094456	CMK	blood:	n/a
18	chr4:76094406-76094456	HIPEpiC	eye:	n/a
19	chr4:76094406-76094456	ECC-1	luminal epithelium:	n/a
20	chr4:76094406-76094456	NHDF-neo	bronchial:	n/a
21	chr4:76094406-76094456	PFSK-1	brain:	n/a
22	chr4:76094406-76094456	Hela-S3	cervix:	n/a
23	chr4:76094406-76094456	Hepatocyte	liver:	n/a
24	chr4:76094406-76094456	H1-hESC	embryonic stem cell:	embryo
25	chr4:76094406-76094456	MCF10A-Er-Src	breast:	n/a
26	chr4:76094406-76094456	SKMC	muscle:	n/a
27	chr4:76094406-76094456	GM12878	blood:	n/a
28	chr4:76094406-76094456	GM06990	blood:	n/a
29	chr4:76094406-76094456	AoSMC	blood vessel:	n/a
30	chr4:76094406-76094456	GM19239	blood:	n/a
31	chr4:76094406-76094456	T-47D	breast:	n/a
32	chr4:76094406-76094456	HPAEpiC	pulmonary alveolar:	n/a
33	chr4:76094406-76094456	AG04450	lung:	fetal
34	chr4:76094406-76094456	NHBE	bronchial:	n/a
35	chr4:76094406-76094456	HepG2	liver:	n/a
36	chr4:76094406-76094456	IMR90	lung:	fetal
37	chr4:76094406-76094456	NT2-D1	testis:	n/a
38	chr4:76094406-76094456	NH-A	brain:	n/a
39	chr4:76094406-76094456	Jurkat	blood:	n/a
40	chr4:76094406-76094456	HAEpiC	amniotic membrane:	n/a
41	chr4:76094406-76094456	HMEC	breast:	n/a
42	chr4:76094406-76094456	HCT-116	colon:	n/a
43	chr4:76094406-76094456	HL-60	blood:	n/a
44	chr4:76094406-76094456	SK-N-SH_RA	brain:	n/a
45	chr4:76094406-76094456	GM12891	blood:	n/a
46	chr4:76094406-76094456	RPTEC	kidney:	n/a
47	chr4:76094406-76094456	Caco-2	colon:	n/a
48	chr4:76094406-76094456	BJ	skin:	n/a
49	chr4:76094406-76094456	LNCaP	prostate:	n/a
50	chr4:76094406-76094456	HCF	heart:	n/a

(count:2 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr4:76115478..76117516-chr4:76118088..76119671,2	MCF-7	breast:
2	chr4:76115478..76117516-chr4:76118088..76119671,2	MCF-7	breast:

(count:5 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RCHY1-7	chr4:76113725-76113875	ucscGeneNc_uc003hii_2
2	lnc-RCHY1-7	chr4:76110978-76111910	ucscGeneNc_uc003hii_2
3	lnc-PARM1-5	chr4:76120077-76120289	NONHSAT096914
4	lnc-RCHY1-7	chr4:76100209-76101593	ucscGeneNc_uc003hii_2
5	lnc-RCHY1-7	chr4:76114521-76114596	ucscGeneNc_uc003hii_2

No data

Variant related genes	Relation type
ENSG00000250560	TF binding region
ENSG00000250560	CpG island

Extended variants
information (count: 788 )
Associated
traits (count: 80 )

Variant overlapped rSNPs/rCNVs (count:788 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs568236945	chr4:76092421-76092422	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs183226275	chr4:76092423-76092424	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs188708267	chr4:76092474-76092475	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs554119814	chr4:76092492-76092493	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs140747626	chr4:76092519-76092520	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs545528915	chr4:76092530-76092531	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs557727406	chr4:76092598-76092599	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs538627522	chr4:76092609-76092610	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs576091702	chr4:76092621-76092622	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs371621853	chr4:76092637-76092638	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs543483588	chr4:76092643-76092644	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs144640852	chr4:76092670-76092671	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs76446851	chr4:76092686-76092687	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs541978045	chr4:76092707-76092708	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs184980114	chr4:76092746-76092747	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs548368946	chr4:76092767-76092768	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs57079087	chr4:76092806-76092807	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs147445131	chr4:76092814-76092815	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs80061927	chr4:76092841-76092842	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs61165124	chr4:76092925-76092926	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs188096646	chr4:76092969-76092970	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs568180484	chr4:76093002-76093003	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs191622339	chr4:76093049-76093050	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs76693691	chr4:76093066-76093067	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs6854125	chr4:76093074-76093075	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs535652963	chr4:76093078-76093079	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs34469188	chr4:76093087-76093088	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs566021953	chr4:76093143-76093144	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs564765738	chr4:76093161-76093162	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs183764296	chr4:76093180-76093181	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs369395491	chr4:76093183-76093184	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs12642121	chr4:76093188-76093189	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs576010697	chr4:76093227-76093228	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs12512069	chr4:76093228-76093229	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs555051434	chr4:76093244-76093245	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs540861090	chr4:76093255-76093256	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs150007426	chr4:76093272-76093273	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs181887995	chr4:76093278-76093279	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs560303763	chr4:76093289-76093290	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs572681888	chr4:76093357-76093358	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs185396757	chr4:76093365-76093366	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs564594004	chr4:76093371-76093372	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs558662725	chr4:76093374-76093375	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs531743731	chr4:76093375-76093376	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs904086	chr4:76093436-76093437	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs190297088	chr4:76093457-76093458	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs529399353	chr4:76093505-76093506	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs547648529	chr4:76093531-76093532	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs565860354	chr4:76093671-76093672	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs370050743	chr4:76093695-76093696	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:80)

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
Autism	22495311	CNVD
Breast cancer	21858162	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Gastric cancer	21586687	CNVD
lymphocytic leukemia	21291569	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Non-small cell lung cancer	21829676	CNVD
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	17603634	CNVD
Glioblastoma multiforme	21922591	CNVD
Parkinson disease	21956041	CNVD
Mental retardation	20522426	CNVD
delayed speech	20522426	CNVD
growth disorder	20522426	CNVD
Hepatocellular carcinoma	16750200	CNVD
Myxofibrosarcoma	16751306	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Parkinson disease	18923514	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Cancer	21183584	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
Colorectal cancer	16272173	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Lung cancer	19208797	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	21785460	CNVD
Prostate cancer	16573809	CNVD
Osteoporosis	18992858	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Myelodysplastic syndrome	21251322	CNVD
Multiple myeloma	17550852	CNVD
Congenital anomalies of the kidney and urinary tract	18316590	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Myelofibrosis	22110671	CNVD
Abnormal phenotypes	18644119	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Cancer	22429812	CNVD
Intracranial aneurysm	16715129	CNVD
Multiple myeloma	16616336	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	20932292	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:111 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:76092400-76092600	Enhancers	iPS-20b Cell Line	embryonic stem cell
2	chr4:76092600-76093200	Enhancers	HUES64 Cell Line	embryonic stem cell
3	chr4:76092600-76093400	Enhancers	H9 Cell Line	embryonic stem cell
4	chr4:76092600-76093400	Enhancers	Fetal Muscle Leg	muscle
5	chr4:76092600-76094200	Enhancers	iPS-18 Cell Line	embryonic stem cell
6	chr4:76092800-76093000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
7	chr4:76092800-76095000	Enhancers	iPS-15b Cell Line	embryonic stem cell
8	chr4:76093000-76093200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
9	chr4:76093000-76093400	Enhancers	ES-I3 Cell Line	embryonic stem cell
10	chr4:76093200-76093400	Enhancers	H1 Cell Line	embryonic stem cell
11	chr4:76093200-76094000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
12	chr4:76093200-76094200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
13	chr4:76093200-76094200	Weak transcription	HUES64 Cell Line	embryonic stem cell
14	chr4:76093400-76093800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
15	chr4:76093400-76094400	Weak transcription	H1 Cell Line	embryonic stem cell
16	chr4:76093400-76097800	Weak transcription	Fetal Muscle Leg	muscle
17	chr4:76093600-76094600	Enhancers	HUES6 Cell Line	embryonic stem cell
18	chr4:76093600-76095000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
19	chr4:76093800-76094000	Enhancers	HUES48 Cell Line	embryonic stem cell
20	chr4:76093800-76094000	Active TSS	iPS-20b Cell Line	embryonic stem cell
21	chr4:76093800-76095600	Enhancers	ES-I3 Cell Line	embryonic stem cell
22	chr4:76094000-76094600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
23	chr4:76094000-76094800	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
24	chr4:76094000-76094800	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
25	chr4:76094000-76095200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
26	chr4:76094200-76094600	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell
27	chr4:76094200-76095200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
28	chr4:76094200-76095200	Enhancers	HUES64 Cell Line	embryonic stem cell
29	chr4:76094400-76095000	Enhancers	H1 Cell Line	embryonic stem cell
30	chr4:76094400-76095000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
31	chr4:76094600-76095000	Enhancers	iPS-18 Cell Line	embryonic stem cell
32	chr4:76094800-76095400	Enhancers	HUES48 Cell Line	embryonic stem cell
33	chr4:76094800-76095400	Enhancers	iPS-20b Cell Line	embryonic stem cell
34	chr4:76095200-76095400	Enhancers	H9 Cell Line	embryonic stem cell
35	chr4:76095400-76096400	Weak transcription	HUES48 Cell Line	embryonic stem cell
36	chr4:76096400-76096600	Enhancers	HUES48 Cell Line	embryonic stem cell
37	chr4:76097800-76098000	Enhancers	Fetal Muscle Leg	muscle
38	chr4:76097800-76098400	Enhancers	GM12878-XiMat	blood
39	chr4:76104600-76105000	Enhancers	Rectal Mucosa Donor 31	rectum
40	chr4:76105000-76105600	Active TSS	Rectal Mucosa Donor 31	rectum
41	chr4:76105600-76105800	Enhancers	Placenta	Placenta
42	chr4:76105600-76106200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
43	chr4:76105600-76106200	Flanking Active TSS	Rectal Mucosa Donor 31	rectum
44	chr4:76105600-76107000	Active TSS	Duodenum Mucosa	Duodenum
45	chr4:76105600-76107200	Active TSS	Rectal Mucosa Donor 29	rectum
46	chr4:76105800-76106000	Enhancers	Primary B cells from peripheral blood	blood
47	chr4:76105800-76106000	Flanking Active TSS	Adipose Nuclei	Adipose
48	chr4:76105800-76106400	Flanking Active TSS	Placenta	Placenta
49	chr4:76105800-76106600	Enhancers	Stomach Mucosa	stomach
50	chr4:76105800-76106600	Active TSS	HepG2	liver

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