Variant report

Variant	nsv973438
Chromosome Location	chr9:140605557-140618202
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:502)
CpG islands
(count:427)
Chromatin interactive
region (count:8)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:502 , 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	ATF2	chr9:140615735-140616429	GM12878	blood:	n/a	n/a
2	ATF2	chr9:140615932-140616395	GM12878	blood:	n/a	n/a
3	BACH1	chr9:140610803-140610830	K562	blood:	n/a	n/a
4	BATF	chr9:140615522-140615833	GM12878	blood:	n/a	n/a
5	BATF	chr9:140610468-140611052	GM12878	blood:	n/a	n/a
6	BATF	chr9:140615504-140615792	GM12878	blood:	n/a	n/a
7	BATF	chr9:140610458-140611042	GM12878	blood:	n/a	n/a
8	BCL11A	chr9:140615461-140615880	GM12878	blood:	n/a	n/a
9	BCL11A	chr9:140610385-140611128	GM12878	blood:	n/a	n/a
10	BCL11A	chr9:140610384-140611091	GM12878	blood:	n/a	n/a
11	BCL3	chr9:140615844-140616336	GM12878	blood:	n/a	n/a
12	BCL3	chr9:140615753-140616334	GM12878	blood:	n/a	n/a
13	BCL3	chr9:140613611-140613872	GM12878	blood:	n/a	n/a
14	BHLHE40	chr9:140610467-140611054	HepG2	liver:	n/a	n/a
15	BHLHE40	chr9:140615531-140615811	HepG2	liver:	n/a	n/a
16	BRCA1	chr9:140610638-140610691	Hela-S3	cervix:	n/a	n/a
17	BRCA1	chr9:140615519-140615856	Hela-S3	cervix:	n/a	n/a
18	CBX3	chr9:140615473-140615838	K562	blood:	n/a	n/a
19	CBX3	chr9:140615543-140615836	K562	blood:	n/a	n/a
20	CBX3	chr9:140612298-140612850	K562	blood:	n/a	n/a
21	CBX3	chr9:140610334-140611181	K562	blood:	n/a	n/a
22	CBX3	chr9:140610397-140611092	K562	blood:	n/a	n/a
23	CEBPB	chr9:140615685-140615706	Hela-S3	cervix:	n/a	n/a
24	CEBPB	chr9:140610498-140611040	GM12878	blood:	n/a	n/a
25	CEBPB	chr9:140610445-140611185	GM12878	blood:	n/a	n/a
26	CEBPD	chr9:140610462-140611106	K562	blood:	n/a	n/a
27	CHD2	chr9:140615510-140615878	Hela-S3	cervix:	n/a	n/a
28	CHD2	chr9:140610816-140610819	Hela-S3	cervix:	n/a	n/a
29	CHD2	chr9:140615525-140615579	GM12878	blood:	n/a	n/a
30	CTCF	chr9:140616500-140616650	GM12873	blood:	n/a	n/a
31	CTCF	chr9:140610720-140610870	RPTEC	kidney:	n/a	n/a
32	CTCF	chr9:140606160-140606310	GM12874	blood:	n/a	n/a
33	CTCF	chr9:140615560-140615710	Hela-S3	cervix:	n/a	n/a
34	CTCF	chr9:140616440-140616649	Spleen_OC	spleen:	n/a	n/a
35	CTCF	chr9:140610519-140611025	K562	blood:	n/a	n/a
36	CTCF	chr9:140616535-140616559	GM10248	blood:	n/a	n/a
37	CTCF	chr9:140616400-140616550	HRPEpiC	eye:	n/a	n/a
38	CTCF	chr9:140616534-140616592	LNCaP	prostate:	n/a	n/a
39	CTCF	chr9:140615651-140615747	GM10248	blood:	n/a	n/a
40	CTCF	chr9:140616465-140616467	Kidney_OC	kidney:	n/a	n/a
41	CTCF	chr9:140616473-140616601	Kidney_OC	kidney:	n/a	n/a
42	CTCF	chr9:140616535-140616589	HUVEC	blood vessel:	n/a	n/a
43	CTCF	chr9:140606100-140606250	Hela-S3	cervix:	n/a	n/a
44	CTCF	chr9:140606200-140606247	GM19240	blood:	n/a	n/a
45	CTCF	chr9:140615560-140615710	HEEpiC	esophagus:	n/a	n/a
46	CTCF	chr9:140610740-140610890	AG09309	skin:	n/a	n/a
47	CTCF	chr9:140616523-140616559	K562	blood:	n/a	n/a
48	CTCF	chr9:140616468-140616628	GM12878	blood:	n/a	n/a
49	CTCF	chr9:140616495-140616553	GM10266	blood:	n/a	n/a
50	CTCF	chr9:140606169-140606247	MCF-7	breast:	n/a	n/a

(count:427 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:140611316-140611366	GM12891	blood:	n/a
2	chr9:140615230-140615280	Hela-S3	cervix:	n/a
3	chr9:140612442-140612492	SAEC	small airway:	n/a
4	chr9:140612442-140612492	HCPEpiC	choroid plexus:	n/a
5	chr9:140615230-140615280	Caco-2	colon:	n/a
6	chr9:140612442-140612492	MCF-7	breast:	n/a
7	chr9:140615546-140615596	T-47D	breast:	n/a
8	chr9:140612549-140612599	HCF	heart:	n/a
9	chr9:140612442-140612492	AG10803	skin:	n/a
10	chr9:140612549-140612599	HEEpiC	esophagus:	n/a
11	chr9:140612549-140612599	HRPEpiC	eye:	n/a
12	chr9:140605874-140605924	NT2-D1	testis:	n/a
13	chr9:140615230-140615280	SK-N-MC	brain:	n/a
14	chr9:140613912-140613962	SK-N-SH	brain:	n/a
15	chr9:140615230-140615280	AG09319	gingival:	n/a
16	chr9:140605874-140605924	Jurkat	blood:	n/a
17	chr9:140612549-140612599	AG09319	gingival:	n/a
18	chr9:140615230-140615280	GM12878	blood:	n/a
19	chr9:140615546-140615596	Caco-2	colon:	n/a
20	chr9:140613912-140613962	HPAEpiC	pulmonary alveolar:	n/a
21	chr9:140605874-140605924	PANC-1	pancreas:	n/a
22	chr9:140615230-140615280	AoSMC	blood vessel:	n/a
23	chr9:140605874-140605924	IMR90	lung:	fetal
24	chr9:140612442-140612492	GM12891	blood:	n/a
25	chr9:140615230-140615280	BE2_C	brain:	n/a
26	chr9:140612549-140612599	SK-N-SH	brain:	n/a
27	chr9:140615230-140615280	GM12891	blood:	n/a
28	chr9:140613912-140613962	HepG2	liver:	n/a
29	chr9:140611316-140611366	HCF	heart:	n/a
30	chr9:140611316-140611366	Hela-S3	cervix:	n/a
31	chr9:140612549-140612599	HCM	heart:	n/a
32	chr9:140612549-140612599	H1-hESC	embryonic stem cell:	embryo
33	chr9:140612442-140612492	AG09319	gingival:	n/a
34	chr9:140615546-140615596	PFSK-1	brain:	n/a
35	chr9:140612549-140612599	HIPEpiC	eye:	n/a
36	chr9:140612442-140612492	SK-N-SH	brain:	n/a
37	chr9:140613912-140613962	MCF-7	breast:	n/a
38	chr9:140615546-140615596	AG04450	lung:	fetal
39	chr9:140605874-140605924	HEEpiC	esophagus:	n/a
40	chr9:140612442-140612492	IMR90	lung:	fetal
41	chr9:140605874-140605924	K562	blood:	n/a
42	chr9:140611316-140611366	HAEpiC	amniotic membrane:	n/a
43	chr9:140615546-140615596	Hela-S3	cervix:	n/a
44	chr9:140613912-140613962	HCPEpiC	choroid plexus:	n/a
45	chr9:140605874-140605924	BJ	skin:	n/a
46	chr9:140615230-140615280	U87	brain:	n/a
47	chr9:140612549-140612599	BJ	skin:	n/a
48	chr9:140612549-140612599	AG04449	skin:	fetal
49	chr9:140615230-140615280	HRE	kidney:	n/a
50	chr9:140615230-140615280	HUVEC	blood vessel:	n/a

(count:8 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr9:140616597..140619590-chr9:140626319..140628863,2	K562	blood:
2	chr9:140610530..140612311-chr9:140612330..140615282,2	K562	blood:
3	chr9:140598819..140601234-chr9:140602896..140605674,2	K562	blood:
4	chr9:140603940..140605598-chr9:140612744..140614733,2	K562	blood:
5	chr9:140603940..140605598-chr9:140612744..140614733,2	K562	blood:
6	chr9:140571698..140574262-chr9:140609421..140611418,2	K562	blood:
7	chr9:140611220..140613659-chr9:140615717..140618487,3	K562	blood:
8	chr9:140611220..140612891-chr9:140615717..140617300,2	K562	blood:

No data

Variant related genes	Relation type
EHMT1	TF binding region
EHMT1	CpG island
ENSG00000181090	chromatin interactions

Extended variants
information (count: 741 )
Associated
traits (count: 20 )

Variant overlapped rSNPs/rCNVs (count:741 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs537973610	chr9:140605567-140605568	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs191662832	chr9:140605568-140605569	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs7036085	chr9:140605605-140605606	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs533982309	chr9:140605644-140605645	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs565122544	chr9:140605667-140605668	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs113668788	chr9:140605676-140605677	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs181644825	chr9:140605685-140605686	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs527896605	chr9:140605721-140605722	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs547657189	chr9:140605788-140605789	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs572264677	chr9:140605794-140605795	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs185735554	chr9:140605812-140605813	Weak transcription Genic enhancers Strong transcription Enhancers ZNF genes & repeats Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs190058713	chr9:140605826-140605827	Weak transcription Genic enhancers Strong transcription Enhancers ZNF genes & repeats Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs529811480	chr9:140605848-140605849	Weak transcription Genic enhancers Strong transcription Enhancers ZNF genes & repeats Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs182666207	chr9:140605855-140605856	Weak transcription Genic enhancers Strong transcription Enhancers ZNF genes & repeats Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs560055764	chr9:140605907-140605908	Weak transcription Genic enhancers Strong transcription Enhancers ZNF genes & repeats Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs555175036	chr9:140605910-140605911	Weak transcription Genic enhancers Strong transcription Enhancers ZNF genes & repeats Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs146794508	chr9:140605916-140605917	Weak transcription Genic enhancers Strong transcription Enhancers ZNF genes & repeats Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs186945954	chr9:140605938-140605939	Weak transcription Genic enhancers Strong transcription Enhancers ZNF genes & repeats Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs190952114	chr9:140605969-140605970	Weak transcription Genic enhancers Strong transcription Enhancers ZNF genes & repeats Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs4631547	chr9:140605996-140605997	Weak transcription Genic enhancers Strong transcription Enhancers ZNF genes & repeats Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs140477307	chr9:140605999-140606000	Weak transcription Genic enhancers Strong transcription Enhancers ZNF genes & repeats Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs577711657	chr9:140606011-140606012	Weak transcription Genic enhancers Strong transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
23	rs568216890	chr9:140606025-140606026	Weak transcription Genic enhancers Strong transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
24	rs117590310	chr9:140606040-140606041	Weak transcription Genic enhancers Strong transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
25	rs553893408	chr9:140606044-140606045	Weak transcription Genic enhancers Strong transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
26	rs577140157	chr9:140606087-140606088	Weak transcription Genic enhancers Strong transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
27	rs563382497	chr9:140606095-140606096	Weak transcription Genic enhancers Strong transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
28	rs183975601	chr9:140606105-140606106	Weak transcription Genic enhancers Strong transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
29	rs113064462	chr9:140606108-140606109	Weak transcription Genic enhancers Strong transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
30	rs372123043	chr9:140606131-140606132	Weak transcription Genic enhancers Strong transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
31	rs188919085	chr9:140606151-140606152	Weak transcription Genic enhancers Strong transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
32	rs542489354	chr9:140606166-140606167	Weak transcription Genic enhancers Strong transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
33	rs562218021	chr9:140606169-140606170	Weak transcription Genic enhancers Strong transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
34	rs115685693	chr9:140606173-140606174	Weak transcription Genic enhancers Strong transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
35	rs138672188	chr9:140606184-140606185	Weak transcription Genic enhancers Strong transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
36	rs559917300	chr9:140606187-140606188	Weak transcription Genic enhancers Strong transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
37	rs532163224	chr9:140606209-140606210	Weak transcription Genic enhancers Strong transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
38	rs551873337	chr9:140606210-140606211	Weak transcription Genic enhancers Strong transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
39	rs149321021	chr9:140606217-140606218	Weak transcription Genic enhancers Strong transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
40	rs192922828	chr9:140606248-140606249	Weak transcription Genic enhancers Strong transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
41	rs184187330	chr9:140606258-140606259	Weak transcription Genic enhancers Strong transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
42	rs143554587	chr9:140606279-140606280	Weak transcription Genic enhancers Strong transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
43	rs73669134	chr9:140606282-140606283	Weak transcription Genic enhancers Strong transcription Enhancers ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs547896865	chr9:140606283-140606284	Weak transcription Genic enhancers Strong transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
45	rs187364019	chr9:140606324-140606325	Weak transcription Genic enhancers Strong transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
46	rs114668574	chr9:140606337-140606338	Weak transcription Genic enhancers Strong transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
47	rs556594098	chr9:140606364-140606365	Weak transcription Genic enhancers Strong transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
48	rs35115918	chr9:140606374-140606375	Weak transcription Genic enhancers Strong transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
49	rs570368272	chr9:140606424-140606425	Weak transcription Strong transcription ZNF genes & repeats Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs548065524	chr9:140606425-140606426	Weak transcription Strong transcription ZNF genes & repeats Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:20)

Disease	PMID	Source
Leukemia	17361228	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Glioblastoma	16823260	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Cardiac fibroma	18329553	CNVD
Lung cancer	19147751	CNVD
Cervical cancer	17311676	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Gastric cancer	17908304	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Salivary gland adenoid cystic carcinoma	17545515	CNVD
Chordoma	18071362	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Sudden cardiac death	19188705	CNVD
Myoepithelioma	18604193	CNVD
Tuberous sclerosis	19566914	CNVD
Multiple myeloma	16616336	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Mantle cell lymphoma	19029149	CNVD
Breast cancer	21509527	CNVD

Chromatin state (count:903 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:140573000-140638400	Weak transcription	Small Intestine	intestine
2	chr9:140590200-140606000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
3	chr9:140591000-140605600	Weak transcription	Duodenum Smooth Muscle	Duodenum
4	chr9:140594400-140605800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
5	chr9:140594600-140609400	Weak transcription	Pancreatic Islets	Pancreatic Islet
6	chr9:140594800-140605600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
7	chr9:140597200-140605800	Weak transcription	Rectal Mucosa Donor 31	rectum
8	chr9:140597600-140605600	Weak transcription	Brain Angular Gyrus	brain
9	chr9:140597600-140611400	Weak transcription	Colonic Mucosa	Colon
10	chr9:140597600-140618000	Weak transcription	NH-A	brain
11	chr9:140597800-140605600	Weak transcription	Hela-S3	cervix
12	chr9:140597800-140605800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
13	chr9:140597800-140605800	Weak transcription	Brain Inferior Temporal Lobe	brain
14	chr9:140597800-140605800	Weak transcription	Fetal Intestine Large	intestine
15	chr9:140597800-140606800	Weak transcription	HSMM	muscle
16	chr9:140598000-140605800	Weak transcription	NHLF	lung
17	chr9:140598400-140605800	Weak transcription	Fetal Muscle Leg	muscle
18	chr9:140598600-140605800	Weak transcription	Aorta	Aorta
19	chr9:140598800-140605800	Weak transcription	Psoas Muscle	Psoas
20	chr9:140598800-140606000	Weak transcription	Brain Anterior Caudate	brain
21	chr9:140598800-140649800	Weak transcription	Stomach Mucosa	stomach
22	chr9:140599000-140605800	Weak transcription	Muscle Satellite Cultured Cells	--
23	chr9:140599000-140605800	Weak transcription	HSMMtube	muscle
24	chr9:140600000-140605800	Enhancers	Breast Myoepithelial Primary Cells	Breast
25	chr9:140600200-140608800	Weak transcription	Fetal Brain Male	brain
26	chr9:140600200-140610400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
27	chr9:140600400-140605600	Weak transcription	HUES48 Cell Line	embryonic stem cell
28	chr9:140600400-140605600	Weak transcription	Primary neutrophils fromperipheralblood	blood
29	chr9:140600400-140605600	Weak transcription	Duodenum Mucosa	Duodenum
30	chr9:140600400-140605800	Weak transcription	H9 Cell Line	embryonic stem cell
31	chr9:140600400-140606200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
32	chr9:140600400-140608600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
33	chr9:140600400-140618200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
34	chr9:140600800-140608600	Weak transcription	K562	blood
35	chr9:140601000-140605600	Weak transcription	Primary hematopoietic stem cells	blood
36	chr9:140601000-140605600	Weak transcription	Adipose Nuclei	Adipose
37	chr9:140601000-140606000	Weak transcription	Fetal Thymus	thymus
38	chr9:140601000-140606400	Weak transcription	GM12878-XiMat	blood
39	chr9:140601000-140612800	Weak transcription	Fetal Kidney	kidney
40	chr9:140601800-140608000	Strong transcription	Monocytes-CD14+_RO01746	blood
41	chr9:140602000-140605600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
42	chr9:140602000-140605600	Weak transcription	Brain Substantia Nigra	brain
43	chr9:140602000-140611200	Weak transcription	Placenta Amnion	Placenta Amnion
44	chr9:140602000-140611400	Weak transcription	Brain Hippocampus Middle	brain
45	chr9:140602200-140611600	Weak transcription	Colon Smooth Muscle	Colon
46	chr9:140602400-140605600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
47	chr9:140602400-140605600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
48	chr9:140603000-140605800	Enhancers	Ovary	ovary
49	chr9:140603200-140606200	Strong transcription	Primary hematopoietic stem cells short term culture	blood
50	chr9:140603200-140608600	Strong transcription	Fetal Intestine Small	intestine

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