Variant report

Variant	nsv1013242
Chromosome Location	chr3:158275578-158305894
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:415)
CpG islands
(count:855)
Chromatin interactive
region (count:15)
LncRNA
region (count:18)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:415 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr3:158288831-158289023	HepG2	liver:	n/a	n/a
2	ATF1	chr3:158288707-158289119	K562	blood:	n/a	chr3:158288896-158288910
3	ATF1	chr3:158277971-158278165	K562	blood:	n/a	n/a
4	ATF3	chr3:158288798-158289061	K562	blood:	n/a	chr3:158288900-158288908 chr3:158288899-158288910 chr3:158288899-158288907 chr3:158288896-158288909 chr3:158288888-158288908 chr3:158288896-158288911 chr3:158288940-158288954 chr3:158288900-158288910 chr3:158288897-158288907 chr3:158288900-158288910 chr3:158288900-158288907 chr3:158288897-158288910 chr3:158288898-158288909 chr3:158288896-158288907
5	BHLHE40	chr3:158288656-158289396	K562	blood:	n/a	n/a
6	BHLHE40	chr3:158296588-158296601	GM12878	blood:	n/a	n/a
7	BRCA1	chr3:158288767-158289388	H1-hESC	embryonic stem cell:	n/a	n/a
8	BRCA1	chr3:158288631-158289011	HepG2	liver:	n/a	n/a
9	BRCA1	chr3:158288820-158289092	GM12878	blood:	n/a	n/a
10	BRCA1	chr3:158288446-158288534	H1-hESC	embryonic stem cell:	n/a	n/a
11	CBX3	chr3:158288527-158289669	K562	blood:	n/a	n/a
12	CBX3	chr3:158291568-158291926	K562	blood:	n/a	n/a
13	CBX3	chr3:158289746-158290237	K562	blood:	n/a	n/a
14	CBX3	chr3:158288743-158289150	K562	blood:	n/a	n/a
15	CCNT2	chr3:158288723-158289095	K562	blood:	n/a	n/a
16	CEBPB	chr3:158288740-158288969	HepG2	liver:	n/a	n/a
17	CEBPB	chr3:158288723-158289071	IMR90	lung:	n/a	n/a
18	CEBPB	chr3:158286171-158286386	K562	blood:	n/a	n/a
19	CEBPB	chr3:158288697-158289043	H1-hESC	embryonic stem cell:	n/a	n/a
20	CEBPB	chr3:158288740-158289047	K562	blood:	n/a	n/a
21	CEBPB	chr3:158296234-158296460	A549	lung:	n/a	n/a
22	CHD2	chr3:158288874-158289010	HepG2	liver:	n/a	n/a
23	CHD2	chr3:158288645-158289280	H1-hESC	embryonic stem cell:	n/a	n/a
24	CHD2	chr3:158289990-158290115	K562	blood:	n/a	n/a
25	CHD2	chr3:158288762-158289135	GM12878	blood:	n/a	n/a
26	CHD2	chr3:158288608-158289399	K562	blood:	n/a	n/a
27	CREB1	chr3:158288638-158289201	ECC-1	luminal epithelium:	n/a	chr3:158288897-158288910
28	CREB1	chr3:158288549-158289377	K562	blood:	n/a	chr3:158288897-158288910
29	CREB1	chr3:158288607-158289288	K562	blood:	n/a	chr3:158288897-158288910
30	CREB1	chr3:158288652-158289242	GM12878	blood:	n/a	chr3:158288897-158288910
31	CREB1	chr3:158288626-158289183	HepG2	liver:	n/a	chr3:158288897-158288910
32	CREB1	chr3:158288651-158289182	H1-hESC	embryonic stem cell:	n/a	chr3:158288897-158288910
33	CREB1	chr3:158288713-158289167	HepG2	liver:	n/a	chr3:158288897-158288910
34	CREB1	chr3:158288664-158289137	ECC-1	luminal epithelium:	n/a	chr3:158288897-158288910
35	CREB1	chr3:158288642-158289327	H1-hESC	embryonic stem cell:	n/a	chr3:158288897-158288910
36	CREB1	chr3:158288619-158289272	A549	lung:	n/a	chr3:158288897-158288910
37	CREB1	chr3:158288708-158289020	A549	lung:	n/a	chr3:158288897-158288910
38	CTCF	chr3:158291706-158291811	ProgFib	skin:	n/a	n/a
39	CTCF	chr3:158291640-158291790	HCFaa	heart:	n/a	n/a
40	CTCF	chr3:158291601-158291841	MCF-7	breast:	n/a	n/a
41	CTCF	chr3:158291568-158291855	K562	blood:	n/a	n/a
42	CTCF	chr3:158291680-158291830	HCT-116	colon:	n/a	n/a
43	CTCF	chr3:158288860-158289010	SAEC	small airway:	n/a	n/a
44	CTCF	chr3:158291680-158291830	HFF-Myc	foreskin:	n/a	n/a
45	CTCF	chr3:158291620-158291770	GM12873	blood:	n/a	n/a
46	CTCF	chr3:158291627-158291804	MCF-7	breast:	n/a	n/a
47	CTCF	chr3:158288932-158288936	GM19239	blood:	n/a	n/a
48	CTCF	chr3:158291680-158291830	A549	lung:	n/a	n/a
49	CTCF	chr3:158291666-158291766	GM12892	blood:	n/a	n/a
50	CTCF	chr3:158288951-158289029	Pancreas_OC	pancreas:	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	chr3:158288887-158288937	ECC-1	luminal epithelium:	n/a
2	chr3:158288887-158288937	ECC-1	luminal epithelium:	n/a
3	chr3:158289160-158289210	RPTEC	kidney:	n/a
4	chr3:158288695-158288745	K562	blood:	n/a
5	chr3:158288872-158288922	BE2_C	brain:	n/a
6	chr3:158288892-158288942	T-47D	breast:	n/a
7	chr3:158286552-158286602	NH-A	brain:	n/a
8	chr3:158290728-158290778	HUVEC	blood vessel:	n/a
9	chr3:158288872-158288922	AG04449	skin:	fetal
10	chr3:158289061-158289111	PrEC	prostate:	n/a
11	chr3:158288837-158288887	GM12891	blood:	n/a
12	chr3:158289160-158289210	ProgFib	skin:	n/a
13	chr3:158289160-158289210	T-47D	breast:	n/a
14	chr3:158288892-158288942	HPAEpiC	pulmonary alveolar:	n/a
15	chr3:158288944-158288994	K562	blood:	n/a
16	chr3:158288837-158288887	NHBE	bronchial:	n/a
17	chr3:158288892-158288942	U87	brain:	n/a
18	chr3:158290728-158290778	BJ	skin:	n/a
19	chr3:158288706-158288756	AG10803	skin:	n/a
20	chr3:158288706-158288756	SK-N-SH_RA	brain:	n/a
21	chr3:158288958-158289008	ECC-1	luminal epithelium:	n/a
22	chr3:158288887-158288937	HUVEC	blood vessel:	n/a
23	chr3:158288680-158288730	SAEC	small airway:	n/a
24	chr3:158289160-158289210	AG09319	gingival:	n/a
25	chr3:158288695-158288745	HAEpiC	amniotic membrane:	n/a
26	chr3:158288680-158288730	NHBE	bronchial:	n/a
27	chr3:158288892-158288942	Jurkat	blood:	n/a
28	chr3:158288695-158288745	IMR90	lung:	fetal
29	chr3:158290728-158290778	SK-N-SH	brain:	n/a
30	chr3:158288872-158288922	AG04450	lung:	fetal
31	chr3:158288872-158288922	NHDF-neo	bronchial:	n/a
32	chr3:158288706-158288756	GM12878	blood:	n/a
33	chr3:158288903-158288953	HCPEpiC	choroid plexus:	n/a
34	chr3:158288680-158288730	IMR90	lung:	fetal
35	chr3:158288706-158288756	RPTEC	kidney:	n/a
36	chr3:158288958-158289008	AoSMC	blood vessel:	n/a
37	chr3:158288958-158289008	HepG2	liver:	n/a
38	chr3:158288958-158289008	BE2_C	brain:	n/a
39	chr3:158290728-158290778	HL-60	blood:	n/a
40	chr3:158288872-158288922	ProgFib	skin:	n/a
41	chr3:158289160-158289210	HNPCEpiC	eye:	n/a
42	chr3:158288944-158288994	MCF-7	breast:	n/a
43	chr3:158288892-158288942	HEK293	kidney:	embryo
44	chr3:158288680-158288730	AoSMC	blood vessel:	n/a
45	chr3:158288837-158288887	H1-hESC	embryonic stem cell:	embryo
46	chr3:158290728-158290778	GM19239	blood:	n/a
47	chr3:158288872-158288922	HIPEpiC	eye:	n/a
48	chr3:158286552-158286602	SK-N-SH	brain:	n/a
49	chr3:158288944-158288994	MCF10A-Er-Src	breast:	n/a
50	chr3:158288903-158288953	BE2_C	brain:	n/a

(count:15 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr3:158284750..158291147-chr3:158359832..158364955,8	K562	blood:
2	chr3:158258697..158261392-chr3:158281959..158283679,2	K562	blood:
3	chr3:158305166..158306746-chr3:158311851..158313623,2	K562	blood:
4	chr3:158278970..158280911-chr3:158284194..158285901,2	K562	blood:
5	chr3:158257580..158259389-chr3:158289106..158290845,2	K562	blood:
6	chr3:158291924..158294331-chr3:158300946..158303373,2	K562	blood:
7	chr3:158269405..158273514-chr3:158275272..158279409,4	K562	blood:
8	chr3:158305166..158306893-chr3:158310417..158313351,2	K562	blood:
9	chr3:158291924..158294331-chr3:158300946..158303373,2	K562	blood:
10	chr3:158278970..158280911-chr3:158284194..158285901,2	K562	blood:
11	chr3:158289477..158292573-chr3:158361739..158363921,4	K562	blood:
12	chr3:158280301..158281909-chr3:158440883..158442429,2	MCF-7	breast:
13	chr3:158291274..158292230-chr3:158361860..158362583,3	MCF-7	breast:
14	chr3:158257580..158259170-chr3:158289106..158290622,2	K562	blood:
15	chr3:158298751..158301229-chr3:158359663..158362148,3	K562	blood:

(count:18 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-LXN-1	chr3:158287960-158288855	ENSG00000243150
2	lnc-LXN-1	chr3:158285749-158285845	NONHSAT092927
3	lnc-LXN-1	chr3:158279186-158279294	ENSG00000243150
4	lnc-LXN-1	chr3:158285749-158285845	ENSG00000243150
5	lnc-LXN-3	chr3:158282151-158283758	ucscGeneNc_uc003fbc_2
6	lnc-LXN-1	chr3:158279186-158279294	NONHSAT092927
7	lnc-LXN-1	chr3:158285749-158285845	NONHSAT092926
8	lnc-LXN-3	chr3:158302418-158302575	ucscGeneNc_uc003fbc_2
9	lnc-LXN-3	chr3:158303841-158303962	ucscGeneNc_uc003fbc_2
10	lnc-MLF1-1	chr3:158282277-158283401	l_2517_chr3:158282276-158289024_testes
11	lnc-RSRC1-1	chr3:158301149-158301620	l_2518_chr3:158290245-158301620_heart
12	lnc-LXN-1	chr3:158288558-158288858	NONHSAT092927
13	lnc-RSRC1-1	chr3:158299962-158300064	l_2518_chr3:158290245-158301620_heart
14	lnc-LXN-1	chr3:158287960-158288012	NONHSAT092927
15	lnc-MLF1-1	chr3:158288770-158289024	l_2517_chr3:158282276-158289024_testes
16	lnc-MLF1-1	chr3:158288342-158288499	l_2517_chr3:158282276-158289024_testes
17	lnc-RSRC1-1	chr3:158290246-158290605	l_2518_chr3:158290245-158301620_heart
18	lnc-LXN-1	chr3:158287960-158288130	NONHSAT092926

No data

Variant related genes	Relation type
ENSG00000243150	TF binding region
MLF1	TF binding region
ENSG00000243150	CpG island
MLF1	CpG island
ENSG00000168827	chromatin interactions
MDM4	miRNA target sites
PHTF1	miRNA target sites
RAB8B	miRNA target sites

Extended variants
information (count: 1083 )
Associated
traits (count: 50 )

Variant overlapped rSNPs/rCNVs (count:1083 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs149947716	chr3:158275605-158275606	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs567086529	chr3:158275628-158275629	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs568262942	chr3:158275640-158275641	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs191131123	chr3:158275648-158275649	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs145112339	chr3:158275649-158275650	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs570150155	chr3:158275708-158275709	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs537121677	chr3:158275761-158275762	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs558602214	chr3:158275781-158275782	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs55720154	chr3:158275810-158275811	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
10	rs1435641	chr3:158275921-158275922	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
11	rs553296923	chr3:158275924-158275925	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs182550730	chr3:158275925-158275926	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs542426844	chr3:158275986-158275987	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs117142873	chr3:158276005-158276006	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs373382756	chr3:158276026-158276027	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs189256595	chr3:158276028-158276029	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs545956283	chr3:158276034-158276035	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs376279839	chr3:158276037-158276038	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs1656370	chr3:158276050-158276051	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs528141724	chr3:158276141-158276142	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs546574576	chr3:158276151-158276152	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs568351745	chr3:158276218-158276219	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs529140760	chr3:158276288-158276289	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs550773938	chr3:158276299-158276300	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs568985069	chr3:158276341-158276342	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs190717526	chr3:158276350-158276351	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs148651912	chr3:158276364-158276365	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs570607047	chr3:158276394-158276395	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs142171453	chr3:158276423-158276424	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs568750972	chr3:158276472-158276473	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs553060263	chr3:158276489-158276490	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs537991042	chr3:158276622-158276623	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs114469175	chr3:158276623-158276624	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs567505190	chr3:158276629-158276630	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs557617688	chr3:158276640-158276641	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs374049231	chr3:158276670-158276671	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs147795139	chr3:158276699-158276700	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs555781147	chr3:158276787-158276788	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs557838690	chr3:158276799-158276800	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs546417504	chr3:158276804-158276805	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs141279275	chr3:158276813-158276814	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs572933729	chr3:158276865-158276866	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs540248032	chr3:158276882-158276883	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs146925646	chr3:158276883-158276884	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs182922356	chr3:158276887-158276888	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs147571477	chr3:158276893-158276894	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs562789318	chr3:158276899-158276900	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs73154340	chr3:158276914-158276915	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
49	rs551112815	chr3:158276926-158276927	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs140724100	chr3:158276936-158276937	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:50)

Disease	PMID	Source
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Glioblastoma multiforme	21080181	CNVD
Retinoblastoma	21504564	CNVD
Medulloblastoma	21979893	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
Squamous cell cancer	20885788	CNVD
Melanoma	18172304	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	22032731	CNVD
Breast cancer	16461572	CNVD
Neuroblastoma	17533364	CNVD
Cervical Cancer	21857958	CNVD
Melanoma	21693616	CNVD
Lung cancer	21426551	CNVD
Cancer	21637783	CNVD
Cervical cancer	21063398	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Oral cancer	21386901	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	22065749	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Basal cell lymphoma	21115979	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Hepatocellular carcinoma	16750200	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Myelodysplastic syndrome	21251322	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Basal cell lymphoma	17170743	CNVD
Breast cancer	16608533	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute myeloid leukemia	20729466	CNVD
Non-small cell lung cancer	19010865	CNVD
abnormal development	18461090	CNVD
Prostate cancer	18632612	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Colorectal cancer	16272173	CNVD
Prostate cancer	16547154	CNVD
Breast cancer	21364760	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:457 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:158256600-158280000	Weak transcription	K562	blood
2	chr3:158260000-158279200	Weak transcription	Left Ventricle	heart
3	chr3:158276800-158277000	Enhancers	Psoas Muscle	Psoas
4	chr3:158277000-158278000	Weak transcription	Psoas Muscle	Psoas
5	chr3:158277400-158279400	Enhancers	Skeletal Muscle Female	skeletal muscle
6	chr3:158278000-158279400	Enhancers	Psoas Muscle	Psoas
7	chr3:158278200-158279400	Enhancers	Skeletal Muscle Male	skeletal muscle
8	chr3:158278600-158280200	Enhancers	Fetal Heart	heart
9	chr3:158278800-158279400	Enhancers	Right Atrium	heart
10	chr3:158279200-158279400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
11	chr3:158279200-158279600	Enhancers	Left Ventricle	heart
12	chr3:158279400-158286200	Weak transcription	Skeletal Muscle Female	skeletal muscle
13	chr3:158279600-158279800	Weak transcription	Left Ventricle	heart
14	chr3:158279800-158280600	Enhancers	Left Ventricle	heart
15	chr3:158280000-158280800	Enhancers	K562	blood
16	chr3:158280200-158280400	Flanking Active TSS	Fetal Heart	heart
17	chr3:158280400-158280600	Enhancers	Fetal Heart	heart
18	chr3:158280600-158280800	Flanking Active TSS	Fetal Heart	heart
19	chr3:158280800-158282400	Enhancers	Fetal Heart	heart
20	chr3:158282400-158285000	Weak transcription	Fetal Heart	heart
21	chr3:158284000-158284400	Enhancers	NHEK	skin
22	chr3:158284200-158284600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
23	chr3:158284200-158284600	Enhancers	Psoas Muscle	Psoas
24	chr3:158284400-158288000	Weak transcription	Brain Angular Gyrus	brain
25	chr3:158284400-158288400	Weak transcription	NHEK	skin
26	chr3:158284600-158288400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
27	chr3:158284600-158288400	Weak transcription	Psoas Muscle	Psoas
28	chr3:158285000-158288400	Enhancers	Fetal Heart	heart
29	chr3:158286200-158286400	Enhancers	Skeletal Muscle Female	skeletal muscle
30	chr3:158286200-158286400	Enhancers	HUVEC	blood vessel
31	chr3:158286400-158287600	Weak transcription	Skeletal Muscle Female	skeletal muscle
32	chr3:158286600-158288400	Weak transcription	HUVEC	blood vessel
33	chr3:158286800-158287000	Enhancers	A549	lung
34	chr3:158286800-158287800	Enhancers	Right Ventricle	heart
35	chr3:158287000-158288200	Enhancers	Skeletal Muscle Male	skeletal muscle
36	chr3:158287200-158288200	Weak transcription	A549	lung
37	chr3:158287600-158287800	Enhancers	Fetal Muscle Trunk	muscle
38	chr3:158287600-158287800	Enhancers	Left Ventricle	heart
39	chr3:158287600-158288400	Enhancers	Fetal Muscle Leg	muscle
40	chr3:158287600-158288400	Enhancers	Skeletal Muscle Female	skeletal muscle
41	chr3:158287600-158288400	Enhancers	K562	blood
42	chr3:158287800-158288200	Enhancers	Brain Hippocampus Middle	brain
43	chr3:158287800-158288200	Enhancers	Ovary	ovary
44	chr3:158287800-158288400	Enhancers	Breast Myoepithelial Primary Cells	Breast
45	chr3:158287800-158288400	Enhancers	Fetal Lung	lung
46	chr3:158287800-158288400	Weak transcription	Right Ventricle	heart
47	chr3:158287800-158288600	Weak transcription	Left Ventricle	heart
48	chr3:158288000-158288200	Enhancers	Brain Anterior Caudate	brain
49	chr3:158288000-158288200	Enhancers	Colon Smooth Muscle	Colon
50	chr3:158288000-158288200	Enhancers	Stomach Smooth Muscle	stomach

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links