Variant report

Variant	nsv878689
Chromosome Location	chr4:9943185-10008305
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:727)
CpG islands
(count:244)
Chromatin interactive
region (count:9)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:727 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:9965207-9965232	HepG2	liver:	n/a	n/a
2	ARID3A	chr4:9952887-9953127	K562	blood:	n/a	n/a
3	ARID3A	chr4:10007887-10008235	HepG2	liver:	n/a	n/a
4	ARID3A	chr4:10004013-10004296	HepG2	liver:	n/a	n/a
5	ARID3A	chr4:9998163-9998719	HepG2	liver:	n/a	n/a
6	ATF2	chr4:10001424-10002312	GM12878	blood:	n/a	n/a
7	ATF2	chr4:9991905-9992354	GM12878	blood:	n/a	n/a
8	ATF2	chr4:10005306-10005725	GM12878	blood:	n/a	n/a
9	ATF2	chr4:10007851-10008196	GM12878	blood:	n/a	n/a
10	ATF2	chr4:10001436-10002278	GM12878	blood:	n/a	n/a
11	ATF2	chr4:10007760-10008278	GM12878	blood:	n/a	n/a
12	ATF2	chr4:9972118-9972587	GM12878	blood:	n/a	n/a
13	ATF3	chr4:10003452-10003631	K562	blood:	n/a	n/a
14	BATF	chr4:9972302-9972703	GM12878	blood:	n/a	n/a
15	BATF	chr4:10001742-10002251	GM12878	blood:	n/a	n/a
16	BATF	chr4:10005411-10005658	GM12878	blood:	n/a	chr4:10005512-10005523
17	BCL11A	chr4:9972312-9972693	GM12878	blood:	n/a	n/a
18	BCL11A	chr4:9972269-9972776	GM12878	blood:	n/a	n/a
19	BCL3	chr4:9991620-9991908	GM12878	blood:	n/a	n/a
20	BCL3	chr4:9989936-9990316	GM12878	blood:	n/a	n/a
21	BCL3	chr4:9991562-9991944	GM12878	blood:	n/a	n/a
22	BCL3	chr4:10005262-10005711	GM12878	blood:	n/a	n/a
23	BCL3	chr4:10007752-10008155	GM12878	blood:	n/a	n/a
24	BCL3	chr4:9989903-9990331	GM12878	blood:	n/a	n/a
25	BCLAF1	chr4:10007701-10008311	GM12878	blood:	n/a	n/a
26	BCLAF1	chr4:9972208-9972590	GM12878	blood:	n/a	n/a
27	BHLHE40	chr4:9972158-9972605	GM12878	blood:	n/a	n/a
28	BHLHE40	chr4:10003903-10004201	GM12878	blood:	n/a	n/a
29	BHLHE40	chr4:10007886-10008835	HepG2	liver:	n/a	n/a
30	BHLHE40	chr4:9964308-9964572	GM12878	blood:	n/a	n/a
31	BHLHE40	chr4:10007812-10009749	GM12878	blood:	n/a	n/a
32	BHLHE40	chr4:9962047-9962396	GM12878	blood:	n/a	n/a
33	BHLHE40	chr4:9983862-9984078	K562	blood:	n/a	n/a
34	BRCA1	chr4:9987308-9987348	GM12878	blood:	n/a	n/a
35	BRCA1	chr4:10008036-10008235	HepG2	liver:	n/a	n/a
36	CEBPB	chr4:10007880-10008127	HepG2	liver:	n/a	n/a
37	CEBPB	chr4:9954044-9954358	K562	blood:	n/a	chr4:9954213-9954224
38	CEBPB	chr4:9954045-9954390	K562	blood:	n/a	chr4:9954213-9954224
39	CEBPB	chr4:9954093-9954373	A549	lung:	n/a	chr4:9954213-9954224
40	CEBPB	chr4:10007842-10008822	HepG2	liver:	n/a	n/a
41	CEBPB	chr4:9964598-9964892	HepG2	liver:	n/a	chr4:9964756-9964767
42	CEBPB	chr4:9954066-9954414	HepG2	liver:	n/a	chr4:9954213-9954224
43	CEBPB	chr4:10007804-10008320	MCF-7	breast:	n/a	n/a
44	CEBPB	chr4:10007844-10008802	HepG2	liver:	n/a	n/a
45	CEBPB	chr4:9999158-9999354	HepG2	liver:	n/a	chr4:9999274-9999285
46	CEBPB	chr4:9954171-9954281	K562	blood:	n/a	chr4:9954213-9954224
47	CEBPB	chr4:10007707-10008323	A549	lung:	n/a	n/a
48	CEBPB	chr4:9954053-9954383	H1-hESC	embryonic stem cell:	n/a	chr4:9954213-9954224
49	CEBPB	chr4:10007854-10008195	A549	lung:	n/a	n/a
50	CEBPB	chr4:10007852-10008196	HepG2	liver:	n/a	n/a

(count:244 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:9990048-9990098	T-47D	breast:	n/a
2	chr4:9998017-9998067	GM12892	blood:	n/a
3	chr4:9990048-9990098	GM12891	blood:	n/a
4	chr4:9998017-9998067	K562	blood:	n/a
5	chr4:9950643-9950693	HCF	heart:	n/a
6	chr4:9950643-9950693	K562	blood:	n/a
7	chr4:9990048-9990098	A549	lung:	n/a
8	chr4:9990048-9990098	HepG2	liver:	n/a
9	chr4:9998017-9998067	U87	brain:	n/a
10	chr4:9998017-9998067	AG04449	skin:	fetal
11	chr4:9998017-9998067	GM19239	blood:	n/a
12	chr4:9998017-9998067	HEK293	kidney:	embryo
13	chr4:9981202-9981252	ovcar-3	ovarian:	n/a
14	chr4:9981202-9981252	SK-N-SH	brain:	n/a
15	chr4:9981202-9981252	HAEpiC	amniotic membrane:	n/a
16	chr4:9998017-9998067	HMEC	breast:	n/a
17	chr4:9990048-9990098	CMK	blood:	n/a
18	chr4:9950643-9950693	PANC-1	pancreas:	n/a
19	chr4:9981202-9981252	PFSK-1	brain:	n/a
20	chr4:9990048-9990098	Caco-2	colon:	n/a
21	chr4:9990048-9990098	SAEC	small airway:	n/a
22	chr4:9998017-9998067	Jurkat	blood:	n/a
23	chr4:9990048-9990098	GM19239	blood:	n/a
24	chr4:9998017-9998067	HEEpiC	esophagus:	n/a
25	chr4:9998017-9998067	AG04450	lung:	fetal
26	chr4:9990048-9990098	LNCaP	prostate:	n/a
27	chr4:9990048-9990098	IMR90	lung:	fetal
28	chr4:9990048-9990098	MCF10A-Er-Src	breast:	n/a
29	chr4:9950643-9950693	NHDF-neo	bronchial:	n/a
30	chr4:9990048-9990098	PFSK-1	brain:	n/a
31	chr4:9998017-9998067	HCPEpiC	choroid plexus:	n/a
32	chr4:9990048-9990098	HNPCEpiC	eye:	n/a
33	chr4:9998017-9998067	HUVEC	blood vessel:	n/a
34	chr4:9990048-9990098	U87	brain:	n/a
35	chr4:9990048-9990098	BE2_C	brain:	n/a
36	chr4:9950643-9950693	GM06990	blood:	n/a
37	chr4:9998017-9998067	AoSMC	blood vessel:	n/a
38	chr4:9990048-9990098	SKMC	muscle:	n/a
39	chr4:9998017-9998067	HL-60	blood:	n/a
40	chr4:9990048-9990098	SK-N-SH	brain:	n/a
41	chr4:9998017-9998067	SKMC	muscle:	n/a
42	chr4:9990048-9990098	Jurkat	blood:	n/a
43	chr4:9998017-9998067	PANC-1	pancreas:	n/a
44	chr4:9990048-9990098	ovcar-3	ovarian:	n/a
45	chr4:9990048-9990098	HCM	heart:	n/a
46	chr4:9998017-9998067	BJ	skin:	n/a
47	chr4:9950643-9950693	HEK293	kidney:	embryo
48	chr4:9990048-9990098	GM06990	blood:	n/a
49	chr4:9998017-9998067	GM12891	blood:	n/a
50	chr4:9950643-9950693	RPTEC	kidney:	n/a

(count:9 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:9957351..9959521-chr4:10008550..10011275,2	MCF-7	breast:
2	chr4:9999663..10002309-chr4:10003898..10006601,3	MCF-7	breast:
3	chr4:10003454..10005588-chr4:10009688..10011673,2	MCF-7	breast:
4	chr4:9959731..9961810-chr4:9971031..9973164,2	K562	blood:
5	chr4:9924672..9926796-chr4:10008145..10009788,2	MCF-7	breast:
6	chr4:9761130..9763005-chr4:9988480..9990175,2	K562	blood:
7	chr4:9959731..9961810-chr4:9971031..9973164,2	K562	blood:
8	chr4:9999663..10002309-chr4:10003898..10006601,3	MCF-7	breast:
9	chr4:9999925..10002392-chr4:10005670..10008448,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-DRD5-2	chr4:10008106-10008316	ENSG00000250413.1

No data

Variant related genes	Relation type
ENSG00000250413	TF binding region
ENSG00000250413	CpG island
ENSG00000250413	chromatin interactions

Extended variants
information (count: 3030 )
Associated
traits (count: 60 )

Variant overlapped rSNPs/rCNVs (count:3030 , 50 per page) page: 1 2 3 4 5 6 7 ... 61

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs13139970	chr4:9943185-9943186	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs146522945	chr4:9943228-9943229	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs577841427	chr4:9943241-9943242	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs545007117	chr4:9943278-9943279	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs560158623	chr4:9943281-9943282	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs571970928	chr4:9943282-9943283	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs542858548	chr4:9943309-9943310	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs552328083	chr4:9943331-9943332	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs561032585	chr4:9943334-9943335	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs113427439	chr4:9943336-9943337	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs531522616	chr4:9943356-9943357	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs188430508	chr4:9943386-9943387	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs113242350	chr4:9943394-9943395	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs549609959	chr4:9943409-9943410	Weak transcription Strong transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs2276965	chr4:9943475-9943476	Weak transcription Strong transcription ZNF genes & repeats Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs375223323	chr4:9943491-9943492	Weak transcription Strong transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs2276964	chr4:9943499-9943500	Weak transcription Strong transcription ZNF genes & repeats Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs373772605	chr4:9943516-9943517	Weak transcription Strong transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs376980125	chr4:9943522-9943523	Weak transcription Strong transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs566828973	chr4:9943527-9943528	Weak transcription Strong transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs373604491	chr4:9943529-9943530	Weak transcription Strong transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs116183067	chr4:9943542-9943543	Weak transcription Strong transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs549642411	chr4:9943555-9943556	Weak transcription Strong transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs112580274	chr4:9943556-9943557	Weak transcription Strong transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs150297497	chr4:9943560-9943561	Weak transcription Strong transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs137954097	chr4:9943573-9943574	Weak transcription Strong transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs367643471	chr4:9943581-9943582	Weak transcription Strong transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs371515376	chr4:9943594-9943595	Weak transcription Strong transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs148602165	chr4:9943618-9943619	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs149454410	chr4:9943624-9943625	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs147545113	chr4:9943625-9943626	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs138526800	chr4:9943629-9943630	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs376107700	chr4:9943635-9943636	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs201690966	chr4:9943674-9943675	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs200826534	chr4:9943695-9943696	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs556832594	chr4:9943698-9943699	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs4292327	chr4:9943700-9943701	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
38	rs373360600	chr4:9943701-9943702	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs538711646	chr4:9943757-9943758	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs142065199	chr4:9943766-9943767	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs571964271	chr4:9943847-9943848	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs76844041	chr4:9943853-9943854	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs369151157	chr4:9943897-9943898	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs112854058	chr4:9943921-9943922	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs536600701	chr4:9943929-9943930	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs77336068	chr4:9943946-9943947	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs543197417	chr4:9943976-9943977	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs151156660	chr4:9943977-9943978	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs532197252	chr4:9943978-9943979	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs558707247	chr4:9943999-9944000	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:60)

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
Glioma	20126413	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:824 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:9911400-9979800	Weak transcription	Duodenum Smooth Muscle	Duodenum
2	chr4:9918600-9948600	Weak transcription	Pancreas	Pancrea
3	chr4:9920200-9943400	Weak transcription	Aorta	Aorta
4	chr4:9926400-9951600	Weak transcription	Spleen	Spleen
5	chr4:9926800-9948000	Weak transcription	Skeletal Muscle Female	skeletal muscle
6	chr4:9927000-9948600	Weak transcription	Right Ventricle	heart
7	chr4:9927800-9948400	Strong transcription	HepG2	liver
8	chr4:9928000-9960000	Weak transcription	Esophagus	oesophagus
9	chr4:9929600-9948600	Weak transcription	Left Ventricle	heart
10	chr4:9929800-9944600	Strong transcription	HMEC	breast
11	chr4:9930600-9946200	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
12	chr4:9930800-9952200	Strong transcription	Primary monocytes fromperipheralblood	blood
13	chr4:9930800-9953800	Strong transcription	Monocytes-CD14+_RO01746	blood
14	chr4:9931000-9944200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
15	chr4:9931000-9946600	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
16	chr4:9931800-9943400	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
17	chr4:9933600-9951200	Strong transcription	Breast Myoepithelial Primary Cells	Breast
18	chr4:9934600-9944600	Strong transcription	Fetal Intestine Large	intestine
19	chr4:9937000-9945800	Strong transcription	Fetal Intestine Small	intestine
20	chr4:9937800-9943200	Weak transcription	Duodenum Mucosa	Duodenum
21	chr4:9938200-9957600	Weak transcription	Fetal Stomach	stomach
22	chr4:9938400-9943400	Weak transcription	Lung	lung
23	chr4:9939600-9956600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
24	chr4:9941000-9948800	Weak transcription	Liver	Liver
25	chr4:9941400-9944000	Strong transcription	NHEK	skin
26	chr4:9941400-9953200	Weak transcription	Stomach Smooth Muscle	stomach
27	chr4:9942000-9949400	Weak transcription	Ovary	ovary
28	chr4:9942200-9948800	Weak transcription	Gastric	stomach
29	chr4:9942600-9945400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
30	chr4:9943000-9944000	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
31	chr4:9943200-9944400	Strong transcription	Duodenum Mucosa	Duodenum
32	chr4:9943400-9943600	ZNF genes & repeats	Aorta	Aorta
33	chr4:9943400-9943600	Enhancers	Placenta Amnion	Placenta Amnion
34	chr4:9943400-9944000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
35	chr4:9943600-9944600	Weak transcription	Aorta	Aorta
36	chr4:9943600-9944600	Weak transcription	Placenta Amnion	Placenta Amnion
37	chr4:9943800-9944400	Weak transcription	Lung	lung
38	chr4:9944000-9944600	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
39	chr4:9944000-9946600	Weak transcription	NHEK	skin
40	chr4:9944000-9979400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
41	chr4:9944200-9944400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
42	chr4:9944400-9948600	Weak transcription	Duodenum Mucosa	Duodenum
43	chr4:9944600-9944800	Enhancers	Lung	lung
44	chr4:9944600-9944800	Enhancers	Placenta Amnion	Placenta Amnion
45	chr4:9944600-9946600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
46	chr4:9944600-9947200	Weak transcription	Fetal Intestine Large	intestine
47	chr4:9944600-9964400	Weak transcription	HMEC	breast
48	chr4:9944800-9945600	Weak transcription	Placenta Amnion	Placenta Amnion
49	chr4:9945400-9945600	Enhancers	Fetal Muscle Trunk	muscle
50	chr4:9945400-9945800	Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived

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