Variant report

Variant	nsv1013161
Chromosome Location	chr4:3903702-4026777
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1956)
CpG islands
(count:855)
Chromatin interactive
region (count:4)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1956 , 50 per page) page: 1 2 3 4 5 6 7 ... 40

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:3956277-3956631	K562	blood:	n/a	n/a
2	ARID3A	chr4:3956305-3956527	HepG2	liver:	n/a	n/a
3	ATF1	chr4:3939560-3939786	K562	blood:	n/a	n/a
4	ATF1	chr4:3957144-3957802	K562	blood:	n/a	n/a
5	ATF1	chr4:3956318-3956561	K562	blood:	n/a	n/a
6	ATF2	chr4:4008103-4008392	H1-hESC	embryonic stem cell:	n/a	n/a
7	ATF2	chr4:4008126-4008444	H1-hESC	embryonic stem cell:	n/a	n/a
8	ATF3	chr4:3956235-3956568	K562	blood:	n/a	n/a
9	ATF3	chr4:4008194-4008377	H1-hESC	embryonic stem cell:	n/a	n/a
10	BATF	chr4:4010229-4010487	GM12878	blood:	n/a	n/a
11	BATF	chr4:3951669-3951946	GM12878	blood:	n/a	n/a
12	BATF	chr4:3939526-3939933	GM12878	blood:	n/a	n/a
13	BATF	chr4:3986555-3986823	GM12878	blood:	n/a	n/a
14	BATF	chr4:3939612-3939927	GM12878	blood:	n/a	n/a
15	BATF	chr4:3986537-3986888	GM12878	blood:	n/a	n/a
16	BATF	chr4:4010220-4010483	GM12878	blood:	n/a	n/a
17	BATF	chr4:3956028-3956299	GM12878	blood:	n/a	n/a
18	BATF	chr4:3956920-3957168	GM12878	blood:	n/a	n/a
19	BATF	chr4:3955991-3956766	GM12878	blood:	n/a	chr4:3956402-3956413 chr4:3956403-3956413
20	BATF	chr4:3941568-3941786	GM12878	blood:	n/a	n/a
21	BATF	chr4:3944161-3944477	GM12878	blood:	n/a	n/a
22	BCL11A	chr4:4010216-4010510	GM12878	blood:	n/a	n/a
23	BCL11A	chr4:3958038-3958427	GM12878	blood:	n/a	n/a
24	BCL11A	chr4:3955392-3955609	GM12878	blood:	n/a	n/a
25	BCL11A	chr4:3951507-3951709	GM12878	blood:	n/a	n/a
26	BCL11A	chr4:3956280-3957206	GM12878	blood:	n/a	chr4:3956853-3956866 chr4:3956401-3956410
27	BCL11A	chr4:3956023-3956272	GM12878	blood:	n/a	n/a
28	BCL11A	chr4:3944113-3944431	GM12878	blood:	n/a	n/a
29	BCL11A	chr4:3986488-3986892	GM12878	blood:	n/a	n/a
30	BCL11A	chr4:3955287-3955742	GM12878	blood:	n/a	n/a
31	BCL11A	chr4:3986608-3986813	GM12878	blood:	n/a	n/a
32	BCL11A	chr4:3956304-3956707	GM12878	blood:	n/a	chr4:3956401-3956410
33	BCL11A	chr4:3939576-3939881	GM12878	blood:	n/a	n/a
34	BCL11A	chr4:3939555-3939890	GM12878	blood:	n/a	n/a
35	BCL11A	chr4:3955998-3956176	GM12878	blood:	n/a	n/a
36	BCL11A	chr4:3956884-3957181	GM12878	blood:	n/a	n/a
37	BCL3	chr4:3912758-3913585	GM12878	blood:	n/a	n/a
38	BCL3	chr4:3912562-3913632	GM12878	blood:	n/a	n/a
39	BHLHE40	chr4:3956985-3956993	K562	blood:	n/a	n/a
40	BHLHE40	chr4:3956981-3957101	HepG2	liver:	n/a	n/a
41	BHLHE40	chr4:3956851-3957841	GM12878	blood:	n/a	n/a
42	BHLHE40	chr4:3956379-3956630	HepG2	liver:	n/a	n/a
43	BHLHE40	chr4:3957474-3957790	HepG2	liver:	n/a	n/a
44	BHLHE40	chr4:3986619-3986903	HepG2	liver:	n/a	n/a
45	BHLHE40	chr4:3956769-3957235	HepG2	liver:	n/a	n/a
46	BHLHE40	chr4:3957428-3957835	K562	blood:	n/a	n/a
47	BHLHE40	chr4:3944248-3944417	GM12878	blood:	n/a	n/a
48	BHLHE40	chr4:3957596-3957797	HepG2	liver:	n/a	n/a
49	BHLHE40	chr4:3956449-3956467	GM12878	blood:	n/a	n/a
50	BHLHE40	chr4:3937661-3937846	K562	blood:	n/a	n/a

(count:855 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:3957584-3957634	AG09319	gingival:	n/a
2	chr4:3957584-3957634	AG09319	gingival:	n/a
3	chr4:3960266-3960316	IMR90	lung:	fetal
4	chr4:3953675-3953725	NB4	blood:	n/a
5	chr4:3960332-3960382	HCPEpiC	choroid plexus:	n/a
6	chr4:3958437-3958487	NHBE	bronchial:	n/a
7	chr4:3956448-3956498	CMK	blood:	n/a
8	chr4:3956448-3956498	HMEC	breast:	n/a
9	chr4:3956448-3956498	GM12878	blood:	n/a
10	chr4:3949662-3949712	GM06990	blood:	n/a
11	chr4:3949662-3949712	AG09309	skin:	n/a
12	chr4:3957584-3957634	HEEpiC	esophagus:	n/a
13	chr4:3948578-3948628	HCPEpiC	choroid plexus:	n/a
14	chr4:3953675-3953725	U87	brain:	n/a
15	chr4:4022850-4022900	IMR90	lung:	fetal
16	chr4:3956963-3957013	HRCEpiC	kidney:	n/a
17	chr4:3958437-3958487	HCM	heart:	n/a
18	chr4:3948578-3948628	Hepatocyte	liver:	n/a
19	chr4:4022850-4022900	HRCEpiC	kidney:	n/a
20	chr4:3956772-3956822	Caco-2	colon:	n/a
21	chr4:3949662-3949712	SK-N-SH_RA	brain:	n/a
22	chr4:3958437-3958487	AG04449	skin:	fetal
23	chr4:3956772-3956822	H1-hESC	embryonic stem cell:	embryo
24	chr4:3948578-3948628	NH-A	brain:	n/a
25	chr4:3960266-3960316	HPAEpiC	pulmonary alveolar:	n/a
26	chr4:3949662-3949712	HCM	heart:	n/a
27	chr4:3948537-3948587	ovcar-3	ovarian:	n/a
28	chr4:3957672-3957722	GM06990	blood:	n/a
29	chr4:4022850-4022900	AG09309	skin:	n/a
30	chr4:3948578-3948628	CMK	blood:	n/a
31	chr4:3948537-3948587	AG09319	gingival:	n/a
32	chr4:4022850-4022900	SKMC	muscle:	n/a
33	chr4:3957665-3957715	AG09319	gingival:	n/a
34	chr4:4022850-4022900	HEEpiC	esophagus:	n/a
35	chr4:3956963-3957013	GM12878	blood:	n/a
36	chr4:3960266-3960316	Hepatocyte	liver:	n/a
37	chr4:3949662-3949712	MCF-7	breast:	n/a
38	chr4:3957665-3957715	HUVEC	blood vessel:	n/a
39	chr4:3960266-3960316	HRE	kidney:	n/a
40	chr4:3957672-3957722	HIPEpiC	eye:	n/a
41	chr4:3956448-3956498	BE2_C	brain:	n/a
42	chr4:3948578-3948628	AG10803	skin:	n/a
43	chr4:3958437-3958487	SK-N-SH_RA	brain:	n/a
44	chr4:3956963-3957013	HMEC	breast:	n/a
45	chr4:3957584-3957634	GM06990	blood:	n/a
46	chr4:3948578-3948628	AoSMC	blood vessel:	n/a
47	chr4:3960266-3960316	LNCaP	prostate:	n/a
48	chr4:3949662-3949712	K562	blood:	n/a
49	chr4:3949662-3949712	H1-hESC	embryonic stem cell:	embryo
50	chr4:3960266-3960316	HAEpiC	amniotic membrane:	n/a

(count:4 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:3952456..3954287-chr4:3955011..3957167,2	MCF-7	breast:
2	chr4:3481517..3483185-chr4:3946552..3949445,2	MCF-7	breast:
3	chr11:67572608..67573347-chr4:3956745..3957344,2	Hela-S3	cervix:
4	chr16:88717065..88717765-chr4:3956553..3957490,2	HCT-116	colon:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-OTOP1-6	chr4:3944759-3945099	NONHSAT094909
2	lnc-OTOP1-6	chr4:3956687-3956728	NONHSAT094909
3	lnc-ADRA2C-1	chr4:3912010-3912331	NONHSAT094899
4	lnc-OTOP1-6	chr4:3952866-3952946	NONHSAT094909
5	lnc-OTOP1-6	chr4:3954838-3954900	NONHSAT094909

No data

Variant related genes	Relation type
ENSG00000253917	TF binding region
ENSG00000249522	TF binding region
ENSG00000271977	TF binding region
FAM86EP	TF binding region
ENPP7P9	TF binding region
OR7E162P	TF binding region
ALG1L7P	TF binding region
ENSG00000253917	CpG island
ENSG00000249522	CpG island
ENSG00000271977	CpG island
FAM86EP	CpG island
ENPP7P9	CpG island
OR7E162P	CpG island
ALG1L7P	CpG island
ENSG00000160172	chromatin interactions
ENSG00000251669	chromatin interactions
ENSG00000253917	chromatin interactions
ENSG00000051523	chromatin interactions

Extended variants
information (count: 6465 )
Associated
traits (count: 57 )

Variant overlapped rSNPs/rCNVs (count:6465 , 50 per page) page: 1 2 3 4 5 6 7 ... 130

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs183566215	chr4:3903726-3903727	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs34027495	chr4:3903746-3903747	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs111824065	chr4:3903776-3903777	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs202141937	chr4:3903777-3903778	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs74202114	chr4:3903814-3903815	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs375061747	chr4:3903815-3903816	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs529833460	chr4:3903844-3903845	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs546272616	chr4:3903867-3903868	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs147310755	chr4:3903885-3903886	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs539294496	chr4:3903919-3903920	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs187912459	chr4:3903922-3903923	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs569443776	chr4:3903936-3903937	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs62289210	chr4:3903945-3903946	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs143346061	chr4:3903961-3903962	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs574827067	chr4:3903968-3903969	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs534349193	chr4:3904017-3904018	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs113583775	chr4:3904046-3904047	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs193213770	chr4:3904057-3904058	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs185234537	chr4:3904063-3904064	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs147542371	chr4:3904081-3904082	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs564859706	chr4:3904086-3904087	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs575187976	chr4:3904099-3904100	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs543988912	chr4:3904112-3904113	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs190142056	chr4:3904117-3904118	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs529753011	chr4:3904118-3904119	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs546680014	chr4:3904122-3904123	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs559856523	chr4:3904130-3904131	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs377052196	chr4:3904148-3904149	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs148391731	chr4:3904159-3904160	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs35928099	chr4:3904183-3904184	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs367903023	chr4:3904190-3904191	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs150956079	chr4:3904195-3904196	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs577302287	chr4:3904216-3904217	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs541103404	chr4:3904217-3904218	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs370601749	chr4:3904219-3904220	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs548494494	chr4:3904248-3904249	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs192766846	chr4:3904283-3904284	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs376401334	chr4:3904304-3904305	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs554257999	chr4:3904305-3904306	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs183937737	chr4:3904331-3904332	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs72502000	chr4:3904359-3904360	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs556173081	chr4:3904363-3904364	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs575179160	chr4:3904442-3904443	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs559716679	chr4:3904470-3904471	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs554422735	chr4:3904486-3904487	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs574587054	chr4:3904517-3904518	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs539919704	chr4:3904519-3904520	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs143359221	chr4:3904526-3904527	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs542914056	chr4:3904539-3904540	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs565546274	chr4:3904550-3904551	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:57)

Disease	PMID	Source
Retinitis pigmentosa	18421352	CNVD
Wolf-Hirschhorn syndrome	19259404	CNVD
Bladder cancer	19242612	CNVD
Breast cancer	19242612	CNVD
Congenital anomalies of the kidney and urinary tract	19242612	CNVD
abnormal development	18461090	CNVD
Olfactory neuroblastoma	18408657	CNVD
Wilms tumour	21544195	CNVD
Melanoma	20688739	CNVD
Colorectal cancer	16272173	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	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
small cell lung cancer	20016488	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Urothelial carcinoma	21177765	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Prostate cancer	18632612	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Breast cancer	21785460	CNVD
Myelofibrosis	22110671	CNVD
Schizophrenia	21399695	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Breast cancer	21509527	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Lung cancer	18438408	CNVD
Ependymoma	20639864	CNVD
Schizophrenia	20967226	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:911 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:3896000-3905000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr4:3897200-3903800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr4:3898200-3906400	Weak transcription	Placenta	Placenta
4	chr4:3898600-3906400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
5	chr4:3903600-3904200	Enhancers	NHDF-Ad	bronchial
6	chr4:3903600-3904800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
7	chr4:3903800-3904200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
8	chr4:3903800-3904200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
9	chr4:3904200-3905000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
10	chr4:3904200-3906400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
11	chr4:3904200-3906400	Weak transcription	NHDF-Ad	bronchial
12	chr4:3904800-3905600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
13	chr4:3905000-3905200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
14	chr4:3905000-3905200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
15	chr4:3905000-3906400	Enhancers	Muscle Satellite Cultured Cells	--
16	chr4:3905000-3907200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
17	chr4:3905200-3906400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
18	chr4:3905200-3907200	Enhancers	Osteobl	bone
19	chr4:3905200-3913000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
20	chr4:3905600-3906400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
21	chr4:3905600-3906400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
22	chr4:3905600-3906800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
23	chr4:3905600-3907000	Enhancers	HSMMtube	muscle
24	chr4:3905600-3907600	Enhancers	HSMM	muscle
25	chr4:3906400-3906600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
26	chr4:3906400-3906800	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
27	chr4:3906400-3906800	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
28	chr4:3906400-3906800	Enhancers	Breast Myoepithelial Primary Cells	Breast
29	chr4:3906400-3906800	Flanking Active TSS	Muscle Satellite Cultured Cells	--
30	chr4:3906400-3907000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
31	chr4:3906400-3907000	Bivalent Enhancer	Skeletal Muscle Female	skeletal muscle
32	chr4:3906400-3907200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
33	chr4:3906400-3907200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
34	chr4:3906400-3907200	Enhancers	Placenta	Placenta
35	chr4:3906400-3907200	Enhancers	NH-A	brain
36	chr4:3906400-3907200	Enhancers	NHDF-Ad	bronchial
37	chr4:3906600-3906800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
38	chr4:3906600-3906800	Enhancers	Adipose Nuclei	Adipose
39	chr4:3906800-3907200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
40	chr4:3906800-3907200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
41	chr4:3906800-3907200	Enhancers	Muscle Satellite Cultured Cells	--
42	chr4:3906800-3907400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
43	chr4:3907200-3911200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
44	chr4:3907200-3911200	Weak transcription	NHDF-Ad	bronchial
45	chr4:3907200-3911800	Weak transcription	Placenta	Placenta
46	chr4:3907200-3912800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
47	chr4:3907400-3912000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
48	chr4:3911200-3912000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
49	chr4:3911200-3913600	Enhancers	NHDF-Ad	bronchial
50	chr4:3911400-3912200	Enhancers	Fetal Adrenal Gland	Adrenal Gland

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