Variant report

Variant	nsv1002437
Chromosome Location	chr2:97732771-97857915
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1494)
CpG islands
(count:1774)
Chromatin interactive
region (count:11)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1494 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:97778081-97778339	HepG2	liver:	n/a	n/a
2	ARID3A	chr2:97778120-97778444	K562	blood:	n/a	n/a
3	ARID3A	chr2:97778807-97778948	HepG2	liver:	n/a	n/a
4	ARID3A	chr2:97778812-97778979	K562	blood:	n/a	n/a
5	ATF1	chr2:97778135-97778323	K562	blood:	n/a	n/a
6	ATF1	chr2:97760434-97760794	K562	blood:	n/a	n/a
7	ATF1	chr2:97807805-97807929	K562	blood:	n/a	n/a
8	ATF3	chr2:97778756-97778914	K562	blood:	n/a	n/a
9	ATF3	chr2:97778056-97778311	GM12878	blood:	n/a	n/a
10	BACH1	chr2:97831358-97831389	H1-hESC	embryonic stem cell:	n/a	n/a
11	BACH1	chr2:97778797-97778986	H1-hESC	embryonic stem cell:	n/a	n/a
12	BATF	chr2:97777979-97778283	GM12878	blood:	n/a	n/a
13	BATF	chr2:97779034-97779410	GM12878	blood:	n/a	n/a
14	BATF	chr2:97760489-97760619	GM12878	blood:	n/a	n/a
15	BATF	chr2:97759887-97760164	GM12878	blood:	n/a	n/a
16	BCL11A	chr2:97759908-97760372	GM12878	blood:	n/a	n/a
17	BCL11A	chr2:97778042-97778304	GM12878	blood:	n/a	chr2:97778076-97778083
18	BCL11A	chr2:97780056-97780285	GM12878	blood:	n/a	n/a
19	BCL11A	chr2:97778616-97779385	GM12878	blood:	n/a	chr2:97778799-97778812 chr2:97778886-97778899
20	BCLAF1	chr2:97778704-97779122	GM12878	blood:	n/a	chr2:97778799-97778812 chr2:97778886-97778899
21	BHLHE40	chr2:97778670-97778987	GM12878	blood:	n/a	chr2:97778882-97778898
22	BHLHE40	chr2:97778996-97779445	HepG2	liver:	n/a	n/a
23	BHLHE40	chr2:97778115-97778317	GM12878	blood:	n/a	n/a
24	BHLHE40	chr2:97778783-97778959	K562	blood:	n/a	chr2:97778882-97778898
25	BRCA1	chr2:97779217-97779560	Hela-S3	cervix:	n/a	chr2:97779322-97779329
26	BRCA1	chr2:97778112-97778312	Hela-S3	cervix:	n/a	n/a
27	BRCA1	chr2:97760435-97760807	Hela-S3	cervix:	n/a	n/a
28	CBX3	chr2:97778007-97778486	K562	blood:	n/a	n/a
29	CBX3	chr2:97779000-97779465	K562	blood:	n/a	n/a
30	CBX3	chr2:97760424-97760767	K562	blood:	n/a	n/a
31	CBX3	chr2:97764654-97764925	K562	blood:	n/a	n/a
32	CBX3	chr2:97778594-97779624	K562	blood:	n/a	n/a
33	CEBPB	chr2:97773446-97773645	IMR90	lung:	n/a	chr2:97773565-97773576
34	CEBPB	chr2:97778777-97779401	Hela-S3	cervix:	n/a	n/a
35	CEBPB	chr2:97799578-97799766	HepG2	liver:	n/a	chr2:97799651-97799662
36	CEBPB	chr2:97773450-97773635	HepG2	liver:	n/a	chr2:97773565-97773576
37	CEBPB	chr2:97773431-97773709	K562	blood:	n/a	chr2:97773565-97773576
38	CEBPB	chr2:97779104-97779603	K562	blood:	n/a	n/a
39	CEBPB	chr2:97773440-97773636	K562	blood:	n/a	chr2:97773565-97773576
40	CEBPD	chr2:97778701-97779156	K562	blood:	n/a	n/a
41	CEBPD	chr2:97778691-97779170	HepG2	liver:	n/a	n/a
42	CHD2	chr2:97760599-97760634	Hela-S3	cervix:	n/a	n/a
43	CHD2	chr2:97778828-97779405	HepG2	liver:	n/a	chr2:97779346-97779356
44	CHD2	chr2:97778673-97779488	Hela-S3	cervix:	n/a	chr2:97779346-97779356
45	CHD2	chr2:97778790-97779380	GM12878	blood:	n/a	chr2:97779346-97779356
46	CREB1	chr2:97778691-97779100	A549	lung:	n/a	n/a
47	CREB1	chr2:97760524-97760708	A549	lung:	n/a	n/a
48	CREB1	chr2:97760499-97760714	A549	lung:	n/a	n/a
49	CREB1	chr2:97760530-97760694	H1-hESC	embryonic stem cell:	n/a	n/a
50	CTCF	chr2:97778740-97778890	GM12871	blood:	n/a	chr2:97778820-97778833

(count:1774 , 50 per page) page: 1 2 3 4 5 6 7 ... 36

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:97760745-97760795	HRPEpiC	eye:	n/a
2	chr2:97760610-97760660	HIPEpiC	eye:	n/a
3	chr2:97761334-97761384	PrEC	prostate:	n/a
4	chr2:97778470-97778520	HCPEpiC	choroid plexus:	n/a
5	chr2:97760612-97760662	NH-A	brain:	n/a
6	chr2:97760745-97760795	HRPEpiC	eye:	n/a
7	chr2:97760610-97760660	HIPEpiC	eye:	n/a
8	chr2:97761334-97761384	PrEC	prostate:	n/a
9	chr2:97778470-97778520	HCPEpiC	choroid plexus:	n/a
10	chr2:97760612-97760662	NH-A	brain:	n/a
11	chr2:97778912-97778962	SAEC	small airway:	n/a
12	chr2:97783139-97783189	HUVEC	blood vessel:	n/a
13	chr2:97778927-97778977	HCT-116	colon:	n/a
14	chr2:97778817-97778867	HNPCEpiC	eye:	n/a
15	chr2:97779411-97779461	K562	blood:	n/a
16	chr2:97760610-97760660	GM06990	blood:	n/a
17	chr2:97778608-97778658	AG04450	lung:	fetal
18	chr2:97778470-97778520	ECC-1	luminal epithelium:	n/a
19	chr2:97778817-97778867	T-47D	breast:	n/a
20	chr2:97778174-97778224	MCF-7	breast:	n/a
21	chr2:97779044-97779094	HCT-116	colon:	n/a
22	chr2:97760745-97760795	PANC-1	pancreas:	n/a
23	chr2:97756352-97756402	U87	brain:	n/a
24	chr2:97760610-97760660	Hela-S3	cervix:	n/a
25	chr2:97760726-97760776	ECC-1	luminal epithelium:	n/a
26	chr2:97778927-97778977	IMR90	lung:	fetal
27	chr2:97778608-97778658	GM12878	blood:	n/a
28	chr2:97760610-97760660	Hepatocyte	liver:	n/a
29	chr2:97760610-97760660	HRPEpiC	eye:	n/a
30	chr2:97776919-97776969	HepG2	liver:	n/a
31	chr2:97779044-97779094	PrEC	prostate:	n/a
32	chr2:97759501-97759551	HEK293	kidney:	embryo
33	chr2:97779565-97779615	HRE	kidney:	n/a
34	chr2:97761843-97761893	GM12878	blood:	n/a
35	chr2:97759501-97759551	AG09309	skin:	n/a
36	chr2:97778927-97778977	HIPEpiC	eye:	n/a
37	chr2:97761354-97761404	IMR90	lung:	fetal
38	chr2:97760749-97760799	PrEC	prostate:	n/a
39	chr2:97778608-97778658	GM12891	blood:	n/a
40	chr2:97760610-97760660	ovcar-3	ovarian:	n/a
41	chr2:97779411-97779461	SK-N-SH_RA	brain:	n/a
42	chr2:97779519-97779569	HRE	kidney:	n/a
43	chr2:97759501-97759551	SK-N-MC	brain:	n/a
44	chr2:97776919-97776969	HRCEpiC	kidney:	n/a
45	chr2:97760745-97760795	GM12892	blood:	n/a
46	chr2:97761843-97761893	SK-N-MC	brain:	n/a
47	chr2:97779784-97779834	T-47D	breast:	n/a
48	chr2:97779519-97779569	HIPEpiC	eye:	n/a
49	chr2:97760612-97760662	MCF-7	breast:	n/a
50	chr2:97778927-97778977	HMEC	breast:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr2:97522364..97524649-chr2:97747761..97749583,2	MCF-7	breast:
2	chr2:97523665..97525724-chr2:97777402..97779360,2	MCF-7	breast:
3	chr2:97777932..97778642-chr2:114147602..114148330,3	MCF-7	breast:
4	chr2:97480158..97482561-chr2:97778545..97780856,2	MCF-7	breast:
5	chr2:97778139..97778659-chr2:114147598..114148210,2	K562	blood:
6	chr2:97405027..97406967-chr2:97777321..97779642,2	K562	blood:
7	chr2:97778136..97778658-chr2:114147633..114148424,9	MCF-7	breast:
8	chr2:97522570..97524502-chr2:97776940..97779479,2	MCF-7	breast:
9	chr2:97625836..97626837-chr2:97777734..97778610,3	MCF-7	breast:
10	chr2:97677657..97678211-chr2:97777841..97778623,2	K562	blood:
11	chr2:97753095..97754963-chr2:97759459..97762136,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ANKRD36-5	chr2:97747330-97748385	NONHSAT072606
2	lnc-ANKRD36-3	chr2:97766321-97766609	NONHSAT072609

No data

Variant related genes	Relation type
ENSG00000188383	TF binding region
FAHD2B	TF binding region
RN7SL313P	TF binding region
ANKRD36	TF binding region
ENSG00000188383	CpG island
FAHD2B	CpG island
RN7SL313P	CpG island
ANKRD36	CpG island
ENSG00000213337	chromatin interactions
ENSG00000114988	chromatin interactions
ENSG00000144199	chromatin interactions
ENSG00000163126	chromatin interactions
ENSG00000168763	chromatin interactions

Extended variants
information (count: 4881 )
Associated
traits (count: 58 )

Variant overlapped rSNPs/rCNVs (count:4881 , 50 per page) page: 1 2 3 4 5 6 7 ... 98

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs79843497	chr2:97732785-97732786	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs562196277	chr2:97732786-97732787	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs75165896	chr2:97732788-97732789	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs78676202	chr2:97732812-97732813	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs112928392	chr2:97732821-97732822	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs3028097	chr2:97732822-97732823	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs35326451	chr2:97732823-97732824	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs58986769	chr2:97732825-97732826	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs146139242	chr2:97732826-97732827	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs527983231	chr2:97732867-97732868	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs79634170	chr2:97732872-97732873	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs77903986	chr2:97732900-97732901	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs77646349	chr2:97732911-97732912	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs547815057	chr2:97732912-97732913	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs144002938	chr2:97732950-97732951	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs371320483	chr2:97732990-97732991	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs550271500	chr2:97732995-97732996	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs62155534	chr2:97733022-97733023	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs570178571	chr2:97733057-97733058	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs537998301	chr2:97733098-97733099	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs62155535	chr2:97733115-97733116	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs548409933	chr2:97733183-97733184	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs62155536	chr2:97733203-97733204	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs568213658	chr2:97733244-97733245	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs534087214	chr2:97733269-97733270	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs79530734	chr2:97733295-97733296	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs553818150	chr2:97733300-97733301	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs576742285	chr2:97733302-97733303	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs72945135	chr2:97733318-97733319	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs539060505	chr2:97733322-97733323	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs1148580	chr2:97733335-97733336	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
32	rs575732955	chr2:97733339-97733340	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs368023801	chr2:97733340-97733341	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs541570683	chr2:97733363-97733364	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs562299042	chr2:97733371-97733372	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs62155537	chr2:97733384-97733385	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs572585113	chr2:97733417-97733418	ZNF genes & repeats Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
38	rs62155538	chr2:97733429-97733430	ZNF genes & repeats Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
39	rs541688149	chr2:97733452-97733453	ZNF genes & repeats Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
40	rs369755950	chr2:97733454-97733455	ZNF genes & repeats Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
41	rs62155539	chr2:97733470-97733471	ZNF genes & repeats Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
42	rs117052612	chr2:97733514-97733515	ZNF genes & repeats Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
43	rs550208135	chr2:97733520-97733521	ZNF genes & repeats Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
44	rs62155540	chr2:97733524-97733525	ZNF genes & repeats Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
45	rs77981723	chr2:97733602-97733603	ZNF genes & repeats Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs386648407	chr2:97733606-97733607	ZNF genes & repeats Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs77295427	chr2:97733608-97733609	ZNF genes & repeats Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs188562693	chr2:97733609-97733610	ZNF genes & repeats Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs75178649	chr2:97733620-97733621	ZNF genes & repeats Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs75297061	chr2:97733626-97733627	ZNF genes & repeats Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:58)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Breast cancer	17603634	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Ependymoma	16718352	CNVD
Prostate cancer	18632612	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Autism	17483303	CNVD
Medulloblastoma	20607354	CNVD
Autism	22495311	CNVD
Autism	18522746	CNVD
Neurodevelopmental disorder	22521361	CNVD
Melanoma	18172304	CNVD
Cancer	16751803	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Seminomas	18059402	CNVD
Testicular germ cell tumor	18059402	CNVD
Myxofibrosarcoma	16751306	CNVD
Breast cancer	16272173	CNVD
Ovarian cancer	21781307	CNVD
Lung cancer	18438408	CNVD
Mowat-Wilson syndrome	21572526	CNVD
Disorders of sex development	21048976	CNVD
epilepsy	18472482	CNVD
Ewing''s sarcoma	17952124	CNVD
Hepatocellular carcinoma	16750200	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Autism	16446308	CNVD
Autism	19401682	CNVD
lymphocytic leukemia	21291569	CNVD
Breast cancer	21509527	CNVD
small cell lung cancer	20016488	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Myelofibrosis	22110671	CNVD
Intellectual disability	22045946	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
Glioblastoma multiforme	21138945	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-small cell lung cancer	16651412	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD

Chromatin state (count:1181 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:97732200-97733200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr2:97732200-97733400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr2:97732600-97734800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
4	chr2:97733200-97733800	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin01	Skin
5	chr2:97733200-97734000	ZNF genes & repeats	Gastric	stomach
6	chr2:97733200-97734200	ZNF genes & repeats	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
7	chr2:97733400-97733800	Bivalent Enhancer	Skeletal Muscle Female	skeletal muscle
8	chr2:97733400-97734000	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
9	chr2:97733400-97734000	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
10	chr2:97733600-97733800	Bivalent Enhancer	Primary hematopoietic stem cells short term culture	blood
11	chr2:97733600-97734000	Enhancers	Brain Germinal Matrix	brain
12	chr2:97733800-97734000	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin
13	chr2:97733800-97734200	Enhancers	Skeletal Muscle Female	skeletal muscle
14	chr2:97734200-97738600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
15	chr2:97738600-97738800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
16	chr2:97744800-97745000	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
17	chr2:97745000-97760600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
18	chr2:97746600-97759800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
19	chr2:97747000-97760600	Weak transcription	Fetal Muscle Leg	muscle
20	chr2:97747200-97760800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
21	chr2:97747400-97749200	Weak transcription	Fetal Stomach	stomach
22	chr2:97747600-97748600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
23	chr2:97747600-97749600	Enhancers	Esophagus	oesophagus
24	chr2:97747600-97759800	Weak transcription	Stomach Smooth Muscle	stomach
25	chr2:97747800-97748000	Enhancers	Brain Hippocampus Middle	brain
26	chr2:97748000-97749400	Weak transcription	Brain Hippocampus Middle	brain
27	chr2:97748000-97759800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
28	chr2:97748000-97760400	Weak transcription	Ovary	ovary
29	chr2:97748000-97760400	Weak transcription	Right Ventricle	heart
30	chr2:97748000-97760600	Weak transcription	Skeletal Muscle Male	skeletal muscle
31	chr2:97748000-97760800	Weak transcription	Brain Substantia Nigra	brain
32	chr2:97748600-97756200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
33	chr2:97748600-97760800	Weak transcription	Brain Cingulate Gyrus	brain
34	chr2:97748600-97761000	Weak transcription	Primary T cells from cord blood	blood
35	chr2:97748800-97760600	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
36	chr2:97749200-97750800	Strong transcription	Fetal Stomach	stomach
37	chr2:97749400-97750200	Strong transcription	Brain Hippocampus Middle	brain
38	chr2:97749800-97759600	Weak transcription	Fetal Brain Female	brain
39	chr2:97750200-97758800	Weak transcription	Brain Hippocampus Middle	brain
40	chr2:97750200-97760800	Weak transcription	Brain Anterior Caudate	brain
41	chr2:97750400-97759600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
42	chr2:97750400-97759800	Weak transcription	Skeletal Muscle Female	skeletal muscle
43	chr2:97750400-97760000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
44	chr2:97750400-97760400	Weak transcription	Left Ventricle	heart
45	chr2:97750600-97759800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
46	chr2:97750600-97760400	Weak transcription	Fetal Muscle Trunk	muscle
47	chr2:97750600-97761400	Weak transcription	Lung	lung
48	chr2:97750800-97757000	Weak transcription	Fetal Stomach	stomach
49	chr2:97750800-97759800	Weak transcription	H9 Cell Line	embryonic stem cell
50	chr2:97750800-97760400	Weak transcription	Primary T regulatory cells fromperipheralblood	blood

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