Variant report

Variant	nsv1001175
Chromosome Location	chr4:9805668-9897520
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:527)
CpG islands
(count:125)
Chromatin interactive
region (count:7)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:527 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr4:9850013-9850273	K562	blood:	n/a	n/a
2	ATF2	chr4:9814641-9815054	GM12878	blood:	n/a	n/a
3	ATF2	chr4:9809744-9810072	GM12878	blood:	n/a	n/a
4	ATF3	chr4:9849946-9850297	K562	blood:	n/a	n/a
5	BACH1	chr4:9806067-9806321	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr4:9885168-9885286	H1-hESC	embryonic stem cell:	n/a	n/a
7	BATF	chr4:9813621-9813815	GM12878	blood:	n/a	n/a
8	BATF	chr4:9814682-9815071	GM12878	blood:	n/a	n/a
9	BATF	chr4:9809777-9810086	GM12878	blood:	n/a	n/a
10	BATF	chr4:9814742-9814999	GM12878	blood:	n/a	n/a
11	BCL11A	chr4:9809742-9810117	GM12878	blood:	n/a	n/a
12	BCL11A	chr4:9814677-9815008	GM12878	blood:	n/a	n/a
13	BCL11A	chr4:9814557-9814998	GM12878	blood:	n/a	n/a
14	BCL11A	chr4:9809752-9810069	GM12878	blood:	n/a	n/a
15	BCL11A	chr4:9851148-9851550	GM12878	blood:	n/a	n/a
16	BCL11A	chr4:9851100-9851523	GM12878	blood:	n/a	n/a
17	BCL3	chr4:9826836-9827129	GM12878	blood:	n/a	n/a
18	BHLHE40	chr4:9851061-9851588	GM12878	blood:	n/a	n/a
19	BHLHE40	chr4:9814583-9815072	GM12878	blood:	n/a	n/a
20	BHLHE40	chr4:9809308-9809346	GM12878	blood:	n/a	n/a
21	BHLHE40	chr4:9872224-9872359	K562	blood:	n/a	n/a
22	BHLHE40	chr4:9882590-9882646	K562	blood:	n/a	n/a
23	BHLHE40	chr4:9867363-9867483	K562	blood:	n/a	n/a
24	BHLHE40	chr4:9809778-9810107	GM12878	blood:	n/a	n/a
25	BRCA1	chr4:9829608-9829617	H1-hESC	embryonic stem cell:	n/a	n/a
26	BRCA1	chr4:9871086-9871272	GM12878	blood:	n/a	n/a
27	CCNT2	chr4:9895028-9895704	K562	blood:	n/a	n/a
28	CEBPB	chr4:9849942-9850300	IMR90	lung:	n/a	chr4:9850045-9850056 chr4:9850120-9850131
29	CEBPB	chr4:9876127-9876348	HepG2	liver:	n/a	chr4:9876241-9876252
30	CEBPB	chr4:9867161-9867312	HepG2	liver:	n/a	chr4:9867238-9867249
31	CEBPB	chr4:9895337-9895676	K562	blood:	n/a	n/a
32	CEBPB	chr4:9849993-9850301	A549	lung:	n/a	chr4:9850045-9850056 chr4:9850120-9850131
33	CEBPB	chr4:9895305-9895547	K562	blood:	n/a	n/a
34	CEBPB	chr4:9849949-9850302	HepG2	liver:	n/a	chr4:9850045-9850056 chr4:9850120-9850131
35	CEBPB	chr4:9849913-9850318	K562	blood:	n/a	chr4:9850045-9850056 chr4:9850120-9850131
36	CEBPB	chr4:9849900-9850296	K562	blood:	n/a	chr4:9850045-9850056 chr4:9850120-9850131
37	CEBPB	chr4:9876209-9876280	K562	blood:	n/a	chr4:9876241-9876252
38	CEBPB	chr4:9849824-9850326	HCT-116	colon:	n/a	chr4:9850045-9850056 chr4:9850120-9850131
39	CEBPB	chr4:9849953-9850289	Hela-S3	cervix:	n/a	chr4:9850045-9850056 chr4:9850120-9850131
40	CEBPB	chr4:9876089-9876404	IMR90	lung:	n/a	chr4:9876241-9876252
41	CEBPB	chr4:9849869-9850308	HCT-116	colon:	n/a	chr4:9850045-9850056 chr4:9850120-9850131
42	CEBPB	chr4:9849998-9850279	K562	blood:	n/a	chr4:9850045-9850056 chr4:9850120-9850131
43	CEBPB	chr4:9888675-9888963	HepG2	liver:	n/a	n/a
44	CEBPB	chr4:9849980-9850299	H1-hESC	embryonic stem cell:	n/a	chr4:9850045-9850056 chr4:9850120-9850131
45	CEBPB	chr4:9849994-9850220	MCF-7	breast:	n/a	chr4:9850045-9850056 chr4:9850120-9850131
46	CEBPD	chr4:9895204-9895804	K562	blood:	n/a	chr4:9895425-9895436
47	CEBPD	chr4:9895295-9895750	K562	blood:	n/a	chr4:9895425-9895436
48	CHD2	chr4:9851191-9851526	GM12878	blood:	n/a	n/a
49	CHD2	chr4:9809751-9810119	GM12878	blood:	n/a	n/a
50	CHD2	chr4:9850691-9850877	GM12878	blood:	n/a	n/a

(count:125 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:9884128-9884178	HRCEpiC	kidney:	n/a
2	chr4:9892887-9892937	GM12891	blood:	n/a
3	chr4:9884128-9884178	HAEpiC	amniotic membrane:	n/a
4	chr4:9884128-9884178	HRCEpiC	kidney:	n/a
5	chr4:9892887-9892937	GM12891	blood:	n/a
6	chr4:9884128-9884178	HAEpiC	amniotic membrane:	n/a
7	chr4:9884128-9884178	PFSK-1	brain:	n/a
8	chr4:9892887-9892937	ovcar-3	ovarian:	n/a
9	chr4:9884128-9884178	ovcar-3	ovarian:	n/a
10	chr4:9892887-9892937	Hepatocyte	liver:	n/a
11	chr4:9892887-9892937	HNPCEpiC	eye:	n/a
12	chr4:9892887-9892937	PrEC	prostate:	n/a
13	chr4:9892887-9892937	H1-hESC	embryonic stem cell:	embryo
14	chr4:9884128-9884178	NT2-D1	testis:	n/a
15	chr4:9884128-9884178	AG09309	skin:	n/a
16	chr4:9892887-9892937	SK-N-SH	brain:	n/a
17	chr4:9884128-9884178	HCM	heart:	n/a
18	chr4:9884128-9884178	BE2_C	brain:	n/a
19	chr4:9884128-9884178	Caco-2	colon:	n/a
20	chr4:9884128-9884178	T-47D	breast:	n/a
21	chr4:9892887-9892937	ProgFib	skin:	n/a
22	chr4:9884128-9884178	AG09319	gingival:	n/a
23	chr4:9884128-9884178	GM12878	blood:	n/a
24	chr4:9892887-9892937	NB4	blood:	n/a
25	chr4:9884128-9884178	GM12892	blood:	n/a
26	chr4:9892887-9892937	AG09309	skin:	n/a
27	chr4:9884128-9884178	Hela-S3	cervix:	n/a
28	chr4:9892887-9892937	BJ	skin:	n/a
29	chr4:9884128-9884178	MCF-7	breast:	n/a
30	chr4:9884128-9884178	AG04449	skin:	fetal
31	chr4:9884128-9884178	IMR90	lung:	fetal
32	chr4:9892887-9892937	Hela-S3	cervix:	n/a
33	chr4:9892887-9892937	HPAEpiC	pulmonary alveolar:	n/a
34	chr4:9892887-9892937	HCF	heart:	n/a
35	chr4:9892887-9892937	RPTEC	kidney:	n/a
36	chr4:9884128-9884178	A549	lung:	n/a
37	chr4:9892887-9892937	HepG2	liver:	n/a
38	chr4:9892887-9892937	GM06990	blood:	n/a
39	chr4:9884128-9884178	Hepatocyte	liver:	n/a
40	chr4:9892887-9892937	AG10803	skin:	n/a
41	chr4:9892887-9892937	A549	lung:	n/a
42	chr4:9892887-9892937	MCF-7	breast:	n/a
43	chr4:9892887-9892937	U87	brain:	n/a
44	chr4:9892887-9892937	SAEC	small airway:	n/a
45	chr4:9884128-9884178	AoSMC	blood vessel:	n/a
46	chr4:9892887-9892937	GM12892	blood:	n/a
47	chr4:9884128-9884178	LNCaP	prostate:	n/a
48	chr4:9892887-9892937	NT2-D1	testis:	n/a
49	chr4:9892887-9892937	T-47D	breast:	n/a
50	chr4:9892887-9892937	HAEpiC	amniotic membrane:	n/a

(count:7 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:9841356..9843538-chr4:9847251..9848935,2	K562	blood:
2	chr4:9869830..9872812-chr4:9880250..9882960,2	K562	blood:
3	chr4:9865151..9867306-chr4:9868074..9870913,3	MCF-7	breast:
4	chr4:9827283..9829135-chr4:9829200..9831465,2	K562	blood:
5	chr4:9869830..9872812-chr4:9880250..9882960,2	K562	blood:
6	chr4:9865151..9867306-chr4:9868074..9870913,3	MCF-7	breast:
7	chr4:9841356..9843538-chr4:9847251..9848935,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-DRD5-13	chr4:9814207-9814604	NONHSAT095145
2	lnc-WDR1-12	chr4:9873428-9874487	NONHSAT095146
3	lnc-DRD5-13	chr4:9807330-9807762	NONHSAT095145
4	lnc-DRD5-13	chr4:9810799-9811038	NONHSAT095145
5	lnc-WDR1-12	chr4:9870401-9871383	NONHSAT095146

No data

Variant related genes	Relation type
SLC2A9	TF binding region
SLC2A9	CpG island
ENSG00000109667	chromatin interactions

Extended variants
information (count: 4143 )
Associated
traits (count: 65 )

Variant overlapped rSNPs/rCNVs (count:4143 , 50 per page) page: 1 2 3 4 5 6 7 ... 83

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs572705873	chr4:9805727-9805728	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs189944150	chr4:9805731-9805732	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs76257144	chr4:9805733-9805734	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs569972929	chr4:9805782-9805783	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs377399577	chr4:9805805-9805806	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs76519353	chr4:9805809-9805810	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs182210204	chr4:9805820-9805821	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs16888811	chr4:9805821-9805822	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs186546542	chr4:9805822-9805823	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs545463557	chr4:9805850-9805851	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs1519096	chr4:9805872-9805873	Strong transcription Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs191223205	chr4:9805873-9805874	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs542625052	chr4:9805941-9805942	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs61404533	chr4:9805945-9805946	Strong transcription Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs371007595	chr4:9805959-9805960	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs184165954	chr4:9805960-9805961	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs565460109	chr4:9805989-9805990	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs532623018	chr4:9806006-9806007	Enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs573908948	chr4:9806027-9806028	Enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs188762603	chr4:9806029-9806030	Enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs565678031	chr4:9806032-9806033	Enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs544404333	chr4:9806067-9806068	Enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs115124464	chr4:9806079-9806080	Enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs548209248	chr4:9806094-9806095	Enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs201420660	chr4:9806121-9806122	Enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs537356888	chr4:9806144-9806145	Enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs193197972	chr4:9806177-9806178	Enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs570624512	chr4:9806211-9806212	Enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs534557814	chr4:9806223-9806224	Enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs185021027	chr4:9806247-9806248	Enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs572450981	chr4:9806342-9806343	Enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs140726714	chr4:9806364-9806365	Enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs554560166	chr4:9806377-9806378	Enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs553470736	chr4:9806381-9806382	Enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs188698472	chr4:9806405-9806406	Enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs543685098	chr4:9806406-9806407	Enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs77759711	chr4:9806411-9806412	Enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs113723750	chr4:9806438-9806439	Enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs145618225	chr4:9806480-9806481	Enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs368596850	chr4:9806506-9806507	Enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs541274682	chr4:9806532-9806533	Enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs191687877	chr4:9806541-9806542	Enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs529833909	chr4:9806561-9806562	Enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs545931207	chr4:9806649-9806650	Enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs148088474	chr4:9806679-9806680	Enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs563256809	chr4:9806680-9806681	Enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs530570496	chr4:9806681-9806682	Enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs141865926	chr4:9806690-9806691	Enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs571871470	chr4:9806745-9806746	Enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs570666938	chr4:9806768-9806769	Enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:65)

Disease	PMID	Source
Wilms tumour	21544195	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
T-cell prolymphocytic leukemia	19278963	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
Chronic lymphocytic leukemia	20421269	CNVD
Breast cancer	21509527	CNVD
Lung cancer	18438408	CNVD
Myelofibrosis	22110671	CNVD
Hirschsprung''s Disease	21712996	CNVD
Schizophrenia	22241247	CNVD
Autosomal-dominant microtia	18179897	CNVD
Glioma	17123091	CNVD
Colorectal cancer	20459617	CNVD
Breast cancer	17133270	CNVD
Sezary syndrome	18413736	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Breast cancer	21858162	CNVD
small cell lung cancer	20016488	CNVD
Neuroblastoma	20406844	CNVD
early-passage human iPS cells	21368824	CNVD
Sinonasal adenocarcinoma	21360264	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Breast cancer	17142309	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Glioma	20126413	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Obesity	21131291	CNVD
Schizophrenia	23813976	CNVD
Hepatocellular carcinoma	22267523	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:482 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:9794600-9805800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
2	chr4:9794600-9812600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr4:9797200-9806400	Weak transcription	HepG2	liver
4	chr4:9798800-9815000	Weak transcription	Lung	lung
5	chr4:9799200-9819600	Weak transcription	HMEC	breast
6	chr4:9804600-9808800	Weak transcription	Primary monocytes fromperipheralblood	blood
7	chr4:9805800-9807000	Strong transcription	Breast Myoepithelial Primary Cells	Breast
8	chr4:9806000-9806800	Enhancers	HUES64 Cell Line	embryonic stem cell
9	chr4:9806000-9807000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
10	chr4:9806200-9806600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
11	chr4:9806200-9806800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
12	chr4:9806200-9807000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
13	chr4:9806200-9821200	Weak transcription	Fetal Intestine Small	intestine
14	chr4:9806400-9807200	Enhancers	Placenta	Placenta
15	chr4:9806400-9807400	Strong transcription	HepG2	liver
16	chr4:9806600-9807000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
17	chr4:9806800-9807000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
18	chr4:9807000-9808800	Weak transcription	Monocytes-CD14+_RO01746	blood
19	chr4:9807000-9809400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
20	chr4:9807000-9810400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
21	chr4:9807000-9819800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
22	chr4:9807200-9807600	Weak transcription	Placenta	Placenta
23	chr4:9807400-9808600	Weak transcription	HepG2	liver
24	chr4:9807600-9808200	Enhancers	Placenta	Placenta
25	chr4:9808200-9809600	ZNF genes & repeats	Placenta	Placenta
26	chr4:9808200-9832000	Weak transcription	Duodenum Mucosa	Duodenum
27	chr4:9808400-9809400	Enhancers	Fetal Stomach	stomach
28	chr4:9808600-9813400	Strong transcription	HepG2	liver
29	chr4:9808800-9810800	Strong transcription	Primary monocytes fromperipheralblood	blood
30	chr4:9808800-9813200	Strong transcription	Monocytes-CD14+_RO01746	blood
31	chr4:9808800-9834400	Weak transcription	NHEK	skin
32	chr4:9809400-9810000	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
33	chr4:9809600-9810000	Enhancers	Fetal Muscle Trunk	muscle
34	chr4:9809600-9810000	Enhancers	Placenta	Placenta
35	chr4:9809600-9810400	Enhancers	Fetal Muscle Leg	muscle
36	chr4:9810000-9830600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
37	chr4:9810400-9811000	Strong transcription	Breast Myoepithelial Primary Cells	Breast
38	chr4:9810800-9811600	Weak transcription	Primary monocytes fromperipheralblood	blood
39	chr4:9811000-9827000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
40	chr4:9811600-9813000	Strong transcription	Primary monocytes fromperipheralblood	blood
41	chr4:9812600-9813600	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
42	chr4:9813000-9813800	Weak transcription	Primary monocytes fromperipheralblood	blood
43	chr4:9813000-9814600	Enhancers	Primary neutrophils fromperipheralblood	blood
44	chr4:9813200-9813400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
45	chr4:9813200-9816000	Weak transcription	Monocytes-CD14+_RO01746	blood
46	chr4:9813400-9814200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
47	chr4:9813400-9826600	Weak transcription	HepG2	liver
48	chr4:9813600-9816000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
49	chr4:9813800-9814400	Enhancers	Primary monocytes fromperipheralblood	blood
50	chr4:9814000-9815000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links