Variant report

Variant	nsv527211
Chromosome Location	chr4:9912101-9944650
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:346)
CpG islands
(count:306)
Chromatin interactive
region (count:10)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:346 , 50 per page) page: 1 2 3 4 5 6 7

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr4:9927280-9927595	K562	blood:	n/a	n/a
2	ATF1	chr4:9929162-9929613	K562	blood:	n/a	n/a
3	BHLHE40	chr4:9920641-9920828	K562	blood:	n/a	n/a
4	BHLHE40	chr4:9937928-9938023	K562	blood:	n/a	n/a
5	CCNT2	chr4:9937760-9938130	K562	blood:	n/a	n/a
6	CEBPB	chr4:9915458-9915692	H1-hESC	embryonic stem cell:	n/a	n/a
7	CEBPB	chr4:9927304-9927536	K562	blood:	n/a	n/a
8	CEBPB	chr4:9927280-9927588	K562	blood:	n/a	n/a
9	CEBPD	chr4:9937797-9938134	K562	blood:	n/a	n/a
10	CHD2	chr4:9943574-9943627	HepG2	liver:	n/a	n/a
11	CHD2	chr4:9944317-9944387	H1-hESC	embryonic stem cell:	n/a	n/a
12	CTCF	chr4:9929420-9929570	HCM	heart:	n/a	n/a
13	CTCF	chr4:9931340-9931490	GM12878	blood:	n/a	n/a
14	CTCF	chr4:9920290-9920322	MCF-7	breast:	n/a	n/a
15	CTCF	chr4:9915642-9915693	H1-hESC	embryonic stem cell:	n/a	n/a
16	CTCF	chr4:9920700-9920850	HMEC	breast:	n/a	n/a
17	CTCF	chr4:9915400-9915550	NHEK	skin:	n/a	n/a
18	CTCF	chr4:9929380-9929530	MCF-7	breast:	n/a	n/a
19	CTCF	chr4:9920720-9920870	WERI-Rb-1	eye:	n/a	n/a
20	CTCF	chr4:9920242-9920367	GM12878	blood:	n/a	n/a
21	CTCF	chr4:9915560-9915710	GM12865	blood:	n/a	n/a
22	CTCF	chr4:9944640-9944790	K562	blood:	n/a	n/a
23	CTCF	chr4:9915641-9915693	GM12891	blood:	n/a	n/a
24	CTCF	chr4:9931300-9931450	GM12875	blood:	n/a	n/a
25	CTCF	chr4:9929361-9929528	MCF-7	breast:	n/a	n/a
26	CTCF	chr4:9929380-9929530	GM12873	blood:	n/a	n/a
27	CTCF	chr4:9915560-9915710	GM12878	blood:	n/a	n/a
28	CTCF	chr4:9915640-9915653	MCF-7	breast:	n/a	n/a
29	CTCF	chr4:9929400-9929550	HRE	kidney:	n/a	n/a
30	CTCF	chr4:9929340-9929490	GM12866	blood:	n/a	n/a
31	CTCF	chr4:9929408-9929509	NHEK	skin:	n/a	n/a
32	CTCF	chr4:9929351-9929504	T-47D	breast:	n/a	n/a
33	CTCF	chr4:9929295-9929620	GM12878	blood:	n/a	n/a
34	CTCF	chr4:9915540-9915690	GM12875	blood:	n/a	n/a
35	CTCF	chr4:9929367-9929535	MCF-7	breast:	n/a	n/a
36	CTCF	chr4:9915600-9915716	GM12892	blood:	n/a	n/a
37	CTCF	chr4:9915240-9915390	GM12871	blood:	n/a	chr4:9915301-9915314
38	CTCF	chr4:9929320-9929470	GM12874	blood:	n/a	n/a
39	CTCF	chr4:9920780-9920930	HEK293	kidney:	n/a	n/a
40	CTCF	chr4:9929340-9929490	AG10803	skin:	n/a	n/a
41	CTCF	chr4:9929380-9929530	HepG2	liver:	n/a	n/a
42	CTCF	chr4:9931382-9931453	LNCaP	prostate:	n/a	n/a
43	CTCF	chr4:9929375-9929539	K562	blood:	n/a	n/a
44	CTCF	chr4:9929410-9929464	HepG2	liver:	n/a	n/a
45	CTCF	chr4:9929374-9929536	GM12878	blood:	n/a	n/a
46	CTCF	chr4:9915540-9915690	GM12874	blood:	n/a	n/a
47	CTCF	chr4:9931340-9931490	HCPEpiC	choroid plexus:	n/a	n/a
48	CTCF	chr4:9929389-9929506	H1-hESC	embryonic stem cell:	n/a	n/a
49	CTCF	chr4:9920740-9920890	K562	blood:	n/a	n/a
50	CTCF	chr4:9915580-9915730	GM12866	blood:	n/a	n/a

(count:306 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:9922462-9922512	MCF-7	breast:	n/a
2	chr4:9922462-9922512	MCF-7	breast:	n/a
3	chr4:9922462-9922512	Hepatocyte	liver:	n/a
4	chr4:9917839-9917889	AG10803	skin:	n/a
5	chr4:9940566-9940616	PrEC	prostate:	n/a
6	chr4:9940566-9940616	BE2_C	brain:	n/a
7	chr4:9926439-9926489	AG04450	lung:	fetal
8	chr4:9922462-9922512	HMEC	breast:	n/a
9	chr4:9922462-9922512	Caco-2	colon:	n/a
10	chr4:9940566-9940616	HCT-116	colon:	n/a
11	chr4:9922462-9922512	HEK293	kidney:	embryo
12	chr4:9940566-9940616	AG09319	gingival:	n/a
13	chr4:9917839-9917889	Hela-S3	cervix:	n/a
14	chr4:9926439-9926489	LNCaP	prostate:	n/a
15	chr4:9922462-9922512	ECC-1	luminal epithelium:	n/a
16	chr4:9926439-9926489	AG10803	skin:	n/a
17	chr4:9940566-9940616	PFSK-1	brain:	n/a
18	chr4:9940566-9940616	ovcar-3	ovarian:	n/a
19	chr4:9940566-9940616	BJ	skin:	n/a
20	chr4:9922462-9922512	HIPEpiC	eye:	n/a
21	chr4:9940566-9940616	HRPEpiC	eye:	n/a
22	chr4:9937674-9937724	SK-N-SH_RA	brain:	n/a
23	chr4:9917839-9917889	HIPEpiC	eye:	n/a
24	chr4:9937674-9937724	HRCEpiC	kidney:	n/a
25	chr4:9940566-9940616	HCPEpiC	choroid plexus:	n/a
26	chr4:9940566-9940616	AG04449	skin:	fetal
27	chr4:9922462-9922512	GM06990	blood:	n/a
28	chr4:9926439-9926489	HCT-116	colon:	n/a
29	chr4:9917839-9917889	HCT-116	colon:	n/a
30	chr4:9937674-9937724	HCM	heart:	n/a
31	chr4:9922462-9922512	HRE	kidney:	n/a
32	chr4:9940566-9940616	NT2-D1	testis:	n/a
33	chr4:9917839-9917889	H1-hESC	embryonic stem cell:	embryo
34	chr4:9940566-9940616	HCM	heart:	n/a
35	chr4:9926439-9926489	HMEC	breast:	n/a
36	chr4:9940566-9940616	NH-A	brain:	n/a
37	chr4:9940566-9940616	AG04450	lung:	fetal
38	chr4:9926439-9926489	GM12878	blood:	n/a
39	chr4:9922462-9922512	PrEC	prostate:	n/a
40	chr4:9926439-9926489	SK-N-MC	brain:	n/a
41	chr4:9922462-9922512	ovcar-3	ovarian:	n/a
42	chr4:9937674-9937724	MCF10A-Er-Src	breast:	n/a
43	chr4:9940566-9940616	HIPEpiC	eye:	n/a
44	chr4:9940566-9940616	CMK	blood:	n/a
45	chr4:9922462-9922512	HRPEpiC	eye:	n/a
46	chr4:9922462-9922512	PANC-1	pancreas:	n/a
47	chr4:9922462-9922512	HCM	heart:	n/a
48	chr4:9937674-9937724	MCF-7	breast:	n/a
49	chr4:9926439-9926489	Hela-S3	cervix:	n/a
50	chr4:9937674-9937724	SAEC	small airway:	n/a

(count:10 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:9929005..9929948-chr4:10015148..10015863,2	MCF-7	breast:
2	chr4:9924672..9926796-chr4:10008145..10009788,2	MCF-7	breast:
3	chr4:9764866..9765415-chr4:9928949..9929492,2	MCF-7	breast:
4	chr4:9931197..9931753-chr4:10016553..10017073,2	MCF-7	breast:
5	chr4:9931454..9932279-chr4:10015120..10015668,2	MCF-7	breast:
6	chr4:9920436..9923282-chr4:9925910..9928355,2	MCF-7	breast:
7	chr4:9920436..9923282-chr4:9925910..9928355,2	MCF-7	breast:
8	chr4:9903730..9906582-chr4:9912941..9915065,2	MCF-7	breast:
9	chr4:9920609..9921128-chr4:10020066..10020974,2	K562	blood:
10	chr4:9918331..9921142-chr4:10116868..10118418,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-DRD5-1	chr4:9925400-9925770	ENSG00000249219.1
2	lnc-DRD5-1	chr4:9924438-9924574	ENSG00000249219.1

No data

Variant related genes	Relation type
ENSG00000249219	TF binding region
SLC2A9	TF binding region
ENSG00000249219	CpG island
SLC2A9	CpG island
ENSG00000223086	chromatin interactions
ENSG00000109667	chromatin interactions
ENSG00000071127	chromatin interactions

Extended variants
information (count: 1426 )
Associated
traits (count: 57 )

Variant overlapped rSNPs/rCNVs (count:1426 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11934363	chr4:9912101-9912102	Strong transcription Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs115146357	chr4:9912135-9912136	Strong transcription Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs192118297	chr4:9912136-9912137	Strong transcription Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs112469934	chr4:9912137-9912138	Strong transcription Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs552106966	chr4:9912170-9912171	Strong transcription Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs570399254	chr4:9912212-9912213	Strong transcription Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs528245301	chr4:9912221-9912222	Strong transcription Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs528378110	chr4:9912262-9912263	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs546862312	chr4:9912264-9912265	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs6840984	chr4:9912274-9912275	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs148849107	chr4:9912295-9912296	Strong transcription Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs556745806	chr4:9912302-9912303	Strong transcription Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs570084872	chr4:9912336-9912337	Strong transcription Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs376641818	chr4:9912349-9912350	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs537194940	chr4:9912390-9912391	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs184241681	chr4:9912489-9912490	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs575847768	chr4:9912490-9912491	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs577200424	chr4:9912498-9912499	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs551307036	chr4:9912516-9912517	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs541721404	chr4:9912562-9912563	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs553676667	chr4:9912586-9912587	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs76647638	chr4:9912604-9912605	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs542403637	chr4:9912605-9912606	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs143519156	chr4:9912609-9912610	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs6449110	chr4:9912625-9912626	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs374399894	chr4:9912628-9912629	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs188043032	chr4:9912645-9912646	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs1878278	chr4:9912648-9912649	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs528105002	chr4:9912671-9912672	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs112914228	chr4:9912690-9912691	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs546203130	chr4:9912707-9912708	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs567972490	chr4:9912710-9912711	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs529153727	chr4:9912722-9912723	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs571554841	chr4:9912732-9912733	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs552663101	chr4:9912767-9912768	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs73225881	chr4:9912825-9912826	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs537535070	chr4:9912844-9912845	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs192983406	chr4:9912880-9912881	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs367901944	chr4:9912884-9912885	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs148346852	chr4:9912889-9912890	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs566993465	chr4:9912897-9912898	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs553414172	chr4:9912909-9912910	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs372155844	chr4:9912910-9912911	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs575141744	chr4:9912962-9912963	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs141536201	chr4:9912983-9912984	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs28643326	chr4:9912993-9912994	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs575783844	chr4:9913104-9913105	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs147528810	chr4:9913107-9913108	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs549209329	chr4:9913117-9913118	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs572902430	chr4:9913133-9913134	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:57)

Disease	PMID	Source
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
Wilms tumour	21544195	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
Breast cancer	17142309	CNVD
Schizophrenia	23813976	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:323 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:9894000-9917800	Weak transcription	Lung	lung
2	chr4:9897000-9924600	Strong transcription	Breast Myoepithelial Primary Cells	Breast
3	chr4:9903400-9923200	Strong transcription	HepG2	liver
4	chr4:9903600-9916000	Strong transcription	Fetal Intestine Large	intestine
5	chr4:9903600-9928600	Strong transcription	Primary monocytes fromperipheralblood	blood
6	chr4:9903600-9929000	Strong transcription	Monocytes-CD14+_RO01746	blood
7	chr4:9906000-9912800	Weak transcription	Sigmoid Colon	Sigmoid Colon
8	chr4:9907000-9918400	Weak transcription	Left Ventricle	heart
9	chr4:9907200-9919400	Weak transcription	Esophagus	oesophagus
10	chr4:9907400-9916600	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
11	chr4:9907400-9923200	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
12	chr4:9907800-9912200	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
13	chr4:9908000-9943000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
14	chr4:9910000-9914400	Weak transcription	HMEC	breast
15	chr4:9911000-9913000	Weak transcription	Duodenum Mucosa	Duodenum
16	chr4:9911000-9916600	Strong transcription	NHEK	skin
17	chr4:9911400-9912200	Weak transcription	Fetal Intestine Small	intestine
18	chr4:9911400-9916000	Weak transcription	Liver	Liver
19	chr4:9911400-9919400	Weak transcription	Aorta	Aorta
20	chr4:9911400-9920200	Weak transcription	Stomach Smooth Muscle	stomach
21	chr4:9911400-9979800	Weak transcription	Duodenum Smooth Muscle	Duodenum
22	chr4:9912200-9914000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
23	chr4:9912200-9915200	Strong transcription	Fetal Intestine Small	intestine
24	chr4:9912800-9913000	Enhancers	Sigmoid Colon	Sigmoid Colon
25	chr4:9913000-9914400	Strong transcription	Duodenum Mucosa	Duodenum
26	chr4:9913200-9918000	Weak transcription	Right Atrium	heart
27	chr4:9914000-9915000	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
28	chr4:9914000-9917800	Weak transcription	Skeletal Muscle Female	skeletal muscle
29	chr4:9914200-9926000	Weak transcription	Spleen	Spleen
30	chr4:9914400-9919400	Weak transcription	Duodenum Mucosa	Duodenum
31	chr4:9914400-9922800	Strong transcription	HMEC	breast
32	chr4:9915000-9915800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
33	chr4:9915200-9915400	Weak transcription	Fetal Intestine Small	intestine
34	chr4:9915400-9928000	Strong transcription	Fetal Intestine Small	intestine
35	chr4:9915800-9917400	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
36	chr4:9916000-9919600	Weak transcription	Fetal Intestine Large	intestine
37	chr4:9916000-9921200	Strong transcription	Liver	Liver
38	chr4:9916600-9916800	Weak transcription	NHEK	skin
39	chr4:9916600-9917400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
40	chr4:9916800-9918200	Strong transcription	NHEK	skin
41	chr4:9917000-9922600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
42	chr4:9917400-9919600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
43	chr4:9917400-9923400	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
44	chr4:9917600-9918600	Enhancers	Primary neutrophils fromperipheralblood	blood
45	chr4:9917800-9918600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
46	chr4:9917800-9918600	Enhancers	Skeletal Muscle Female	skeletal muscle
47	chr4:9917800-9918800	Enhancers	Lung	lung
48	chr4:9917800-9918800	Enhancers	HSMMtube	muscle
49	chr4:9918000-9918800	Enhancers	Skeletal Muscle Male	skeletal muscle
50	chr4:9918000-9920400	Enhancers	Right Atrium	heart

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