Variant report

Variant	nsv878674
Chromosome Location	chr4:9797703-9900314
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:623)
CpG islands
(count:122)
Chromatin interactive
region (count:11)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:623 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

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	chr4:9809744-9810072	GM12878	blood:	n/a	n/a
3	ATF2	chr4:9814641-9815054	GM12878	blood:	n/a	n/a
4	ATF3	chr4:9849946-9850297	K562	blood:	n/a	n/a
5	BACH1	chr4:9885168-9885286	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr4:9806067-9806321	H1-hESC	embryonic stem cell:	n/a	n/a
7	BATF	chr4:9814742-9814999	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	chr4:9813621-9813815	GM12878	blood:	n/a	n/a
11	BCL11A	chr4:9814677-9815008	GM12878	blood:	n/a	n/a
12	BCL11A	chr4:9809752-9810069	GM12878	blood:	n/a	n/a
13	BCL11A	chr4:9809742-9810117	GM12878	blood:	n/a	n/a
14	BCL11A	chr4:9814557-9814998	GM12878	blood:	n/a	n/a
15	BCL11A	chr4:9851100-9851523	GM12878	blood:	n/a	n/a
16	BCL11A	chr4:9851148-9851550	GM12878	blood:	n/a	n/a
17	BCL3	chr4:9826836-9827129	GM12878	blood:	n/a	n/a
18	BHLHE40	chr4:9872224-9872359	K562	blood:	n/a	n/a
19	BHLHE40	chr4:9809778-9810107	GM12878	blood:	n/a	n/a
20	BHLHE40	chr4:9809308-9809346	GM12878	blood:	n/a	n/a
21	BHLHE40	chr4:9867363-9867483	K562	blood:	n/a	n/a
22	BHLHE40	chr4:9882590-9882646	K562	blood:	n/a	n/a
23	BHLHE40	chr4:9802635-9802910	GM12878	blood:	n/a	n/a
24	BHLHE40	chr4:9851061-9851588	GM12878	blood:	n/a	n/a
25	BHLHE40	chr4:9814583-9815072	GM12878	blood:	n/a	n/a
26	BRCA1	chr4:9829608-9829617	H1-hESC	embryonic stem cell:	n/a	n/a
27	BRCA1	chr4:9871086-9871272	GM12878	blood:	n/a	n/a
28	CCNT2	chr4:9895028-9895704	K562	blood:	n/a	n/a
29	CEBPB	chr4:9849953-9850289	Hela-S3	cervix:	n/a	chr4:9850045-9850056 chr4:9850120-9850131
30	CEBPB	chr4:9849913-9850318	K562	blood:	n/a	chr4:9850045-9850056 chr4:9850120-9850131
31	CEBPB	chr4:9900230-9900797	H1-hESC	embryonic stem cell:	n/a	n/a
32	CEBPB	chr4:9867161-9867312	HepG2	liver:	n/a	chr4:9867238-9867249
33	CEBPB	chr4:9876127-9876348	HepG2	liver:	n/a	chr4:9876241-9876252
34	CEBPB	chr4:9849993-9850301	A549	lung:	n/a	chr4:9850045-9850056 chr4:9850120-9850131
35	CEBPB	chr4:9849980-9850299	H1-hESC	embryonic stem cell:	n/a	chr4:9850045-9850056 chr4:9850120-9850131
36	CEBPB	chr4:9849994-9850220	MCF-7	breast:	n/a	chr4:9850045-9850056 chr4:9850120-9850131
37	CEBPB	chr4:9849949-9850302	HepG2	liver:	n/a	chr4:9850045-9850056 chr4:9850120-9850131
38	CEBPB	chr4:9876209-9876280	K562	blood:	n/a	chr4:9876241-9876252
39	CEBPB	chr4:9895305-9895547	K562	blood:	n/a	n/a
40	CEBPB	chr4:9895337-9895676	K562	blood:	n/a	n/a
41	CEBPB	chr4:9849869-9850308	HCT-116	colon:	n/a	chr4:9850045-9850056 chr4:9850120-9850131
42	CEBPB	chr4:9849942-9850300	IMR90	lung:	n/a	chr4:9850045-9850056 chr4:9850120-9850131
43	CEBPB	chr4:9849824-9850326	HCT-116	colon:	n/a	chr4:9850045-9850056 chr4:9850120-9850131
44	CEBPB	chr4:9849998-9850279	K562	blood:	n/a	chr4:9850045-9850056 chr4:9850120-9850131
45	CEBPB	chr4:9849900-9850296	K562	blood:	n/a	chr4:9850045-9850056 chr4:9850120-9850131
46	CEBPB	chr4:9888675-9888963	HepG2	liver:	n/a	n/a
47	CEBPB	chr4:9876089-9876404	IMR90	lung:	n/a	chr4:9876241-9876252
48	CEBPD	chr4:9895295-9895750	K562	blood:	n/a	chr4:9895425-9895436
49	CEBPD	chr4:9895204-9895804	K562	blood:	n/a	chr4:9895425-9895436
50	CHD2	chr4:9809751-9810119	GM12878	blood:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:9884128-9884178	CMK	blood:	n/a
2	chr4:9892887-9892937	NT2-D1	testis:	n/a
3	chr4:9892887-9892937	HEK293	kidney:	embryo
4	chr4:9892887-9892937	A549	lung:	n/a
5	chr4:9892887-9892937	NH-A	brain:	n/a
6	chr4:9892887-9892937	AG04449	skin:	fetal
7	chr4:9892887-9892937	HCPEpiC	choroid plexus:	n/a
8	chr4:9884128-9884178	HL-60	blood:	n/a
9	chr4:9892887-9892937	HCT-116	colon:	n/a
10	chr4:9892887-9892937	HEEpiC	esophagus:	n/a
11	chr4:9884128-9884178	AG10803	skin:	n/a
12	chr4:9892887-9892937	HRPEpiC	eye:	n/a
13	chr4:9892887-9892937	H1-hESC	embryonic stem cell:	embryo
14	chr4:9892887-9892937	HepG2	liver:	n/a
15	chr4:9892887-9892937	MCF10A-Er-Src	breast:	n/a
16	chr4:9892887-9892937	PrEC	prostate:	n/a
17	chr4:9884128-9884178	NHBE	bronchial:	n/a
18	chr4:9892887-9892937	HPAEpiC	pulmonary alveolar:	n/a
19	chr4:9892887-9892937	GM06990	blood:	n/a
20	chr4:9884128-9884178	HPAEpiC	pulmonary alveolar:	n/a
21	chr4:9884128-9884178	HCF	heart:	n/a
22	chr4:9892887-9892937	IMR90	lung:	fetal
23	chr4:9892887-9892937	BE2_C	brain:	n/a
24	chr4:9884128-9884178	AG09309	skin:	n/a
25	chr4:9892887-9892937	GM12891	blood:	n/a
26	chr4:9884128-9884178	HRPEpiC	eye:	n/a
27	chr4:9892887-9892937	HCF	heart:	n/a
28	chr4:9884128-9884178	BE2_C	brain:	n/a
29	chr4:9892887-9892937	T-47D	breast:	n/a
30	chr4:9884128-9884178	PANC-1	pancreas:	n/a
31	chr4:9892887-9892937	ECC-1	luminal epithelium:	n/a
32	chr4:9892887-9892937	K562	blood:	n/a
33	chr4:9884128-9884178	ovcar-3	ovarian:	n/a
34	chr4:9884128-9884178	ProgFib	skin:	n/a
35	chr4:9884128-9884178	U87	brain:	n/a
36	chr4:9884128-9884178	HCT-116	colon:	n/a
37	chr4:9892887-9892937	Caco-2	colon:	n/a
38	chr4:9892887-9892937	ovcar-3	ovarian:	n/a
39	chr4:9884128-9884178	PFSK-1	brain:	n/a
40	chr4:9884128-9884178	AG04450	lung:	fetal
41	chr4:9884128-9884178	K562	blood:	n/a
42	chr4:9884128-9884178	HAEpiC	amniotic membrane:	n/a
43	chr4:9892887-9892937	LNCaP	prostate:	n/a
44	chr4:9884128-9884178	AG09319	gingival:	n/a
45	chr4:9884128-9884178	Hepatocyte	liver:	n/a
46	chr4:9892887-9892937	NHDF-neo	bronchial:	n/a
47	chr4:9884128-9884178	Hela-S3	cervix:	n/a
48	chr4:9892887-9892937	HNPCEpiC	eye:	n/a
49	chr4:9884128-9884178	SK-N-SH_RA	brain:	n/a
50	chr4:9892887-9892937	SK-N-SH	brain:	n/a

(count:11 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:9827283..9829135-chr4:9829200..9831465,2	K562	blood:
2	chr4:9869830..9872812-chr4:9880250..9882960,2	K562	blood:
3	chr4:9766226..9767390-chr4:9899951..9901032,8	MCF-7	breast:
4	chr4:9764792..9765537-chr4:9899989..9900954,5	MCF-7	breast:
5	chr4:9869830..9872812-chr4:9880250..9882960,2	K562	blood:
6	chr4:9865151..9867306-chr4:9868074..9870913,3	MCF-7	breast:
7	chr4:9898528..9900449-chr4:10019179..10021130,2	MCF-7	breast:
8	chr4:9841356..9843538-chr4:9847251..9848935,2	K562	blood:
9	chr4:9841356..9843538-chr4:9847251..9848935,2	K562	blood:
10	chr4:9766848..9767385-chr4:9900038..9900893,4	MCF-7	breast:
11	chr4:9865151..9867306-chr4:9868074..9870913,3	MCF-7	breast:

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

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

No data

Variant related genes	Relation type
RNA5SP154	TF binding region
SLC2A9	TF binding region
RNA5SP154	CpG island
SLC2A9	CpG island
ENSG00000109667	chromatin interactions

Extended variants
information (count: 4614 )
Associated
traits (count: 67 )

Variant overlapped rSNPs/rCNVs (count:4614 , 50 per page) page: 1 2 3 4 5 6 7 ... 93

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs13106539	chr4:9797703-9797704	Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs527476094	chr4:9797706-9797707	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs548916550	chr4:9797750-9797751	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs190391101	chr4:9797768-9797769	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs182272137	chr4:9797771-9797772	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs550917924	chr4:9797772-9797773	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs569258776	chr4:9797810-9797811	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs539869009	chr4:9797813-9797814	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs558486106	chr4:9797823-9797824	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs567210567	chr4:9797824-9797825	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs534361600	chr4:9797888-9797889	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs555682551	chr4:9797889-9797890	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs141183770	chr4:9797916-9797917	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs184387875	chr4:9797919-9797920	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs552068620	chr4:9798015-9798016	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs556255403	chr4:9798027-9798028	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs189070632	chr4:9798030-9798031	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs146955774	chr4:9798079-9798080	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs559976332	chr4:9798085-9798086	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs2139240	chr4:9798092-9798093	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs181452584	chr4:9798098-9798099	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs138052838	chr4:9798126-9798127	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs113406918	chr4:9798139-9798140	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs550775065	chr4:9798164-9798165	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs569420851	chr4:9798179-9798180	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs377529549	chr4:9798196-9798197	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs2867389	chr4:9798201-9798202	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs554272228	chr4:9798220-9798221	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs533354134	chr4:9798222-9798223	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs2867390	chr4:9798237-9798238	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs2867391	chr4:9798246-9798247	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs2867392	chr4:9798248-9798249	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs185646091	chr4:9798257-9798258	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs3060762	chr4:9798260-9798261	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs567121521	chr4:9798290-9798291	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs10015812	chr4:9798316-9798317	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs377537223	chr4:9798354-9798355	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs555892702	chr4:9798372-9798373	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs150463413	chr4:9798395-9798396	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs138311708	chr4:9798519-9798520	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs58691214	chr4:9798557-9798558	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs149644486	chr4:9798566-9798567	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs577330300	chr4:9798569-9798570	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs544559200	chr4:9798597-9798598	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs61020282	chr4:9798604-9798605	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs6449000	chr4:9798612-9798613	Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs35800794	chr4:9798645-9798646	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs555175537	chr4:9798646-9798647	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs367672511	chr4:9798651-9798652	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs547597979	chr4:9798665-9798666	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:67)

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
Urothelial carcinoma	21177765	CNVD
Neuroblastoma	20406844	CNVD
early-passage human iPS cells	21368824	CNVD
Sinonasal adenocarcinoma	21360264	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Ependymoma	20639864	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:514 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:9794400-9798000	Weak transcription	HMEC	breast
2	chr4:9794600-9805800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
3	chr4:9794600-9812600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr4:9797200-9806400	Weak transcription	HepG2	liver
5	chr4:9798200-9799200	Enhancers	HMEC	breast
6	chr4:9798800-9815000	Weak transcription	Lung	lung
7	chr4:9799200-9802000	Weak transcription	Liver	Liver
8	chr4:9799200-9819600	Weak transcription	HMEC	breast
9	chr4:9802400-9803400	Enhancers	Thymus	Thymus
10	chr4:9802600-9803800	Enhancers	Fetal Thymus	thymus
11	chr4:9803200-9803800	Enhancers	Fetal Muscle Trunk	muscle
12	chr4:9803200-9803800	Enhancers	Fetal Muscle Leg	muscle
13	chr4:9804600-9808800	Weak transcription	Primary monocytes fromperipheralblood	blood
14	chr4:9805800-9807000	Strong transcription	Breast Myoepithelial Primary Cells	Breast
15	chr4:9806000-9806800	Enhancers	HUES64 Cell Line	embryonic stem cell
16	chr4:9806000-9807000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
17	chr4:9806200-9806600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
18	chr4:9806200-9806800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
19	chr4:9806200-9807000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
20	chr4:9806200-9821200	Weak transcription	Fetal Intestine Small	intestine
21	chr4:9806400-9807200	Enhancers	Placenta	Placenta
22	chr4:9806400-9807400	Strong transcription	HepG2	liver
23	chr4:9806600-9807000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
24	chr4:9806800-9807000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
25	chr4:9807000-9808800	Weak transcription	Monocytes-CD14+_RO01746	blood
26	chr4:9807000-9809400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
27	chr4:9807000-9810400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
28	chr4:9807000-9819800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
29	chr4:9807200-9807600	Weak transcription	Placenta	Placenta
30	chr4:9807400-9808600	Weak transcription	HepG2	liver
31	chr4:9807600-9808200	Enhancers	Placenta	Placenta
32	chr4:9808200-9809600	ZNF genes & repeats	Placenta	Placenta
33	chr4:9808200-9832000	Weak transcription	Duodenum Mucosa	Duodenum
34	chr4:9808400-9809400	Enhancers	Fetal Stomach	stomach
35	chr4:9808600-9813400	Strong transcription	HepG2	liver
36	chr4:9808800-9810800	Strong transcription	Primary monocytes fromperipheralblood	blood
37	chr4:9808800-9813200	Strong transcription	Monocytes-CD14+_RO01746	blood
38	chr4:9808800-9834400	Weak transcription	NHEK	skin
39	chr4:9809400-9810000	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
40	chr4:9809600-9810000	Enhancers	Fetal Muscle Trunk	muscle
41	chr4:9809600-9810000	Enhancers	Placenta	Placenta
42	chr4:9809600-9810400	Enhancers	Fetal Muscle Leg	muscle
43	chr4:9810000-9830600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
44	chr4:9810400-9811000	Strong transcription	Breast Myoepithelial Primary Cells	Breast
45	chr4:9810800-9811600	Weak transcription	Primary monocytes fromperipheralblood	blood
46	chr4:9811000-9827000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
47	chr4:9811600-9813000	Strong transcription	Primary monocytes fromperipheralblood	blood
48	chr4:9812600-9813600	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
49	chr4:9813000-9813800	Weak transcription	Primary monocytes fromperipheralblood	blood
50	chr4:9813000-9814600	Enhancers	Primary neutrophils fromperipheralblood	blood

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