Variant report

Variant	esv1839005
Chromosome Location	chr2:96613136-96674509
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:96658477-96658815	K562	blood:	n/a	n/a
2	ARID3A	chr2:96658478-96658839	HepG2	liver:	n/a	n/a
3	ARID3A	chr2:96657356-96657461	HepG2	liver:	n/a	n/a
4	BATF	chr2:96658613-96658920	GM12878	blood:	n/a	n/a
5	BATF	chr2:96657475-96657892	GM12878	blood:	n/a	n/a
6	BATF	chr2:96658639-96658882	GM12878	blood:	n/a	n/a
7	BCL11A	chr2:96657495-96657685	GM12878	blood:	n/a	n/a
8	BCL11A	chr2:96657716-96658282	GM12878	blood:	n/a	chr2:96658121-96658134 chr2:96658034-96658047
9	BCL3	chr2:96662608-96662859	GM12878	blood:	n/a	n/a
10	BCL3	chr2:96662691-96662929	GM12878	blood:	n/a	n/a
11	BHLHE40	chr2:96658011-96658260	HepG2	liver:	n/a	chr2:96658035-96658051
12	BHLHE40	chr2:96658621-96658806	GM12878	blood:	n/a	n/a
13	BHLHE40	chr2:96657453-96657904	HepG2	liver:	n/a	n/a
14	BRCA1	chr2:96657456-96657485	Hela-S3	cervix:	n/a	n/a
15	CBX3	chr2:96657325-96658290	K562	blood:	n/a	n/a
16	CBX3	chr2:96658432-96658923	K562	blood:	n/a	n/a
17	CEBPB	chr2:96646282-96646304	K562	blood:	n/a	n/a
18	CEBPB	chr2:96663348-96663438	H1-hESC	embryonic stem cell:	n/a	chr2:96663356-96663367
19	CEBPB	chr2:96663278-96663518	A549	lung:	n/a	chr2:96663356-96663367
20	CEBPB	chr2:96636977-96637167	IMR90	lung:	n/a	n/a
21	CEBPB	chr2:96636977-96637166	HepG2	liver:	n/a	n/a
22	CEBPB	chr2:96663246-96663537	K562	blood:	n/a	chr2:96663356-96663367
23	CEBPB	chr2:96658611-96658827	Hela-S3	cervix:	n/a	n/a
24	CEBPB	chr2:96663252-96663535	IMR90	lung:	n/a	chr2:96663356-96663367
25	CEBPB	chr2:96663255-96663506	Hela-S3	cervix:	n/a	chr2:96663356-96663367
26	CEBPB	chr2:96658508-96658906	K562	blood:	n/a	n/a
27	CEBPB	chr2:96636979-96637158	K562	blood:	n/a	n/a
28	CEBPB	chr2:96663273-96663531	HepG2	liver:	n/a	chr2:96663356-96663367
29	CEBPB	chr2:96658614-96658651	K562	blood:	n/a	n/a
30	CEBPD	chr2:96657560-96657977	K562	blood:	n/a	n/a
31	CHD1	chr2:96658785-96658800	GM12878	blood:	n/a	n/a
32	CHD1	chr2:96657191-96657571	IMR90	lung:	n/a	n/a
33	CHD2	chr2:96657404-96657454	Hela-S3	cervix:	n/a	n/a
34	CTCF	chr2:96658556-96658840	MCF-7	breast:	n/a	chr2:96658689-96658697 chr2:96658684-96658702 chr2:96658753-96658769 chr2:96658686-96658707 chr2:96658752-96658770 chr2:96658754-96658775
35	CTCF	chr2:96658520-96658670	HPAF	blood vessel:	n/a	n/a
36	CTCF	chr2:96657584-96657712	A549	lung:	n/a	n/a
37	CTCF	chr2:96658472-96658883	ECC-1	luminal epithelium:	n/a	chr2:96658689-96658697 chr2:96658684-96658702 chr2:96658753-96658769 chr2:96658686-96658707 chr2:96658752-96658770 chr2:96658754-96658775
38	CTCF	chr2:96657890-96658228	MCF-7	breast:	n/a	chr2:96658205-96658218 chr2:96658100-96658113
39	CTCF	chr2:96658620-96658770	HUVEC	blood vessel:	n/a	chr2:96658689-96658697 chr2:96658684-96658702 chr2:96658753-96658769 chr2:96658686-96658707 chr2:96658752-96658770
40	CTCF	chr2:96658520-96658670	AG09319	gingival:	n/a	n/a
41	CTCF	chr2:96615120-96615270	NHLF	lung:	n/a	chr2:96615185-96615203 chr2:96615187-96615200
42	CTCF	chr2:96658520-96658670	NHEK	skin:	n/a	n/a
43	CTCF	chr2:96657940-96658238	GM19240	blood:	n/a	chr2:96658205-96658218 chr2:96658100-96658113
44	CTCF	chr2:96657500-96657824	K562	blood:	n/a	n/a
45	CTCF	chr2:96658523-96658910	Lung_OC	lung:	n/a	chr2:96658689-96658697 chr2:96658684-96658702 chr2:96658753-96658769 chr2:96658686-96658707 chr2:96658752-96658770 chr2:96658754-96658775
46	CTCF	chr2:96657630-96657673	GM12892	blood:	n/a	n/a
47	CTCF	chr2:96662939-96662986	GM13976	blood:	n/a	n/a
48	CTCF	chr2:96658260-96658410	Hela-S3	cervix:	n/a	n/a
49	CTCF	chr2:96658313-96659032	A549	lung:	n/a	chr2:96658689-96658697 chr2:96658684-96658702 chr2:96658753-96658769 chr2:96658686-96658707 chr2:96658752-96658770 chr2:96658754-96658775
50	CTCF	chr2:96657880-96658030	HAc	cerebellar:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:96658324-96658374	HCT-116	colon:	n/a
2	chr2:96657403-96657453	U87	brain:	n/a
3	chr2:96673978-96674028	NHBE	bronchial:	n/a
4	chr2:96658648-96658698	PFSK-1	brain:	n/a
5	chr2:96662438-96662488	LNCaP	prostate:	n/a
6	chr2:96657403-96657453	GM19239	blood:	n/a
7	chr2:96658324-96658374	MCF-7	breast:	n/a
8	chr2:96658324-96658374	AG10803	skin:	n/a
9	chr2:96662438-96662488	AG10803	skin:	n/a
10	chr2:96662438-96662488	HEEpiC	esophagus:	n/a
11	chr2:96657403-96657453	NHDF-neo	bronchial:	n/a
12	chr2:96658648-96658698	Caco-2	colon:	n/a
13	chr2:96662438-96662488	HCF	heart:	n/a
14	chr2:96657499-96657549	Hepatocyte	liver:	n/a
15	chr2:96658020-96658070	ProgFib	skin:	n/a
16	chr2:96658020-96658070	GM19239	blood:	n/a
17	chr2:96673978-96674028	SK-N-MC	brain:	n/a
18	chr2:96658324-96658374	AG04450	lung:	fetal
19	chr2:96658324-96658374	H1-hESC	embryonic stem cell:	embryo
20	chr2:96657403-96657453	A549	lung:	n/a
21	chr2:96657403-96657453	MCF-7	breast:	n/a
22	chr2:96658648-96658698	AG04449	skin:	fetal
23	chr2:96673978-96674028	BJ	skin:	n/a
24	chr2:96657499-96657549	CMK	blood:	n/a
25	chr2:96657499-96657549	AG09309	skin:	n/a
26	chr2:96673978-96674028	HCM	heart:	n/a
27	chr2:96658648-96658698	MCF-7	breast:	n/a
28	chr2:96658020-96658070	ovcar-3	ovarian:	n/a
29	chr2:96658020-96658070	HCT-116	colon:	n/a
30	chr2:96658020-96658070	NHDF-neo	bronchial:	n/a
31	chr2:96657403-96657453	SAEC	small airway:	n/a
32	chr2:96662438-96662488	NB4	blood:	n/a
33	chr2:96662438-96662488	SKMC	muscle:	n/a
34	chr2:96662438-96662488	HIPEpiC	eye:	n/a
35	chr2:96662438-96662488	HAEpiC	amniotic membrane:	n/a
36	chr2:96658020-96658070	HL-60	blood:	n/a
37	chr2:96658020-96658070	AG04449	skin:	fetal
38	chr2:96658324-96658374	U87	brain:	n/a
39	chr2:96658324-96658374	HCM	heart:	n/a
40	chr2:96662438-96662488	ProgFib	skin:	n/a
41	chr2:96657403-96657453	ProgFib	skin:	n/a
42	chr2:96657499-96657549	PFSK-1	brain:	n/a
43	chr2:96657403-96657453	SK-N-SH_RA	brain:	n/a
44	chr2:96658020-96658070	SK-N-MC	brain:	n/a
45	chr2:96658324-96658374	HNPCEpiC	eye:	n/a
46	chr2:96657403-96657453	HMEC	breast:	n/a
47	chr2:96657499-96657549	H1-hESC	embryonic stem cell:	embryo
48	chr2:96657403-96657453	HRE	kidney:	n/a
49	chr2:96673978-96674028	MCF-7	breast:	n/a
50	chr2:96658020-96658070	HepG2	liver:	n/a

No.	Distal block	Cell Line	Cell type
1	chr2:96656872..96660081-chr2:96874473..96876452,3	MCF-7	breast:
2	chr2:96658288..96659130-chr2:96839638..96840848,4	MCF-7	breast:
3	chr2:96673991..96676008-chr2:96873030..96875575,2	MCF-7	breast:
4	chr2:96658361..96659117-chr2:98208510..98209019,2	MCF-7	breast:
5	chr2:96656483..96658831-chr2:96781728..96784486,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GPAT2-1	chr2:96626387-96626412	XLOC_002209
2	lnc-GPAT2-3	chr2:96646496-96646533	NONHSAT072524
3	lnc-GPAT2-1	chr2:96616497-96616527	XLOC_002209
4	lnc-GPAT2-1	chr2:96619687-96619753	XLOC_002209
5	lnc-GPAT2-3	chr2:96652506-96652587	NONHSAT072524
6	lnc-GPAT2-3	chr2:96648004-96648112	NONHSAT072524
7	lnc-GPAT2-1	chr2:96622534-96622564	XLOC_002209
8	lnc-GPAT2-1	chr2:96614278-96614344	XLOC_002209
9	lnc-GPAT2-1	chr2:96617096-96617156	XLOC_002209
10	lnc-GPAT2-1	chr2:96624339-96624411	XLOC_002209
11	lnc-GPAT2-3	chr2:96643875-96643937	NONHSAT072524
12	lnc-ANKRD36C-3	chr2:96670313-96670601	NONHSAT072529

Variant related genes	Relation type
RN7SL210P	TF binding region
FAHD2CP	TF binding region
ANKRD36C	TF binding region
RN7SL210P	CpG island
FAHD2CP	CpG island
ANKRD36C	CpG island
ENSG00000084090	chromatin interactions
ENSG00000204685	chromatin interactions
ENSG00000222040	chromatin interactions
B4GALT1	miRNA target sites
BACE1	miRNA target sites

Extended variants
information (count: 2035 )
Associated
traits (count: 52 )

Variant overlapped rSNPs/rCNVs (count:2035 , 50 per page) page: 1 2 3 4 5 6 7 ... 41

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs575433506	chr2:96613144-96613145	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs72935817	chr2:96613151-96613152	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs201893854	chr2:96613196-96613197	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs557142643	chr2:96613207-96613208	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs186672201	chr2:96613258-96613259	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs191483140	chr2:96613262-96613263	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs542702384	chr2:96613326-96613327	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs536207794	chr2:96613365-96613366	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs572963620	chr2:96613389-96613390	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs200207401	chr2:96613462-96613463	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs544990953	chr2:96613465-96613466	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs565170715	chr2:96613500-96613501	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs115855833	chr2:96613514-96613515	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs201162231	chr2:96613515-96613516	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs116148989	chr2:96613520-96613521	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs373056985	chr2:96613579-96613580	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs187659475	chr2:96613601-96613602	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs202065707	chr2:96613634-96613635	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs560906892	chr2:96613635-96613636	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs200538795	chr2:96613655-96613656	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs192896602	chr2:96613672-96613673	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs201154086	chr2:96613716-96613717	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs201634379	chr2:96613731-96613732	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs200181966	chr2:96613736-96613737	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs201257526	chr2:96613766-96613767	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs201842125	chr2:96613785-96613786	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs200278326	chr2:96613786-96613787	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs369546088	chr2:96613817-96613818	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs201613647	chr2:96613835-96613836	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs373134811	chr2:96613843-96613844	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs566967815	chr2:96613845-96613846	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs199570097	chr2:96613853-96613854	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs200294486	chr2:96613889-96613890	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs201429567	chr2:96613895-96613896	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs539210489	chr2:96613903-96613904	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs552625159	chr2:96613923-96613924	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs569531625	chr2:96613930-96613931	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs72492181	chr2:96613941-96613942	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs79994507	chr2:96613958-96613959	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs77759848	chr2:96613972-96613973	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs537086061	chr2:96613975-96613976	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs78161527	chr2:96613992-96613993	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs201919879	chr2:96614015-96614016	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs371300991	chr2:96614017-96614018	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs184614492	chr2:96614026-96614027	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs567222638	chr2:96614030-96614031	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs75362494	chr2:96614074-96614075	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs12105535	chr2:96614089-96614090	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs4243789	chr2:96614092-96614093	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	mRNA abundance
50	rs139182099	chr2:96614105-96614106	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:52)

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
Neuroblastoma	18574593	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
Epilepsy	22083797	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD

Chromatin state (count:517 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:96502800-96616600	Weak transcription	Fetal Stomach	stomach
2	chr2:96556200-96645000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
3	chr2:96556400-96628600	Weak transcription	Sigmoid Colon	Sigmoid Colon
4	chr2:96556400-96645000	Weak transcription	Primary monocytes fromperipheralblood	blood
5	chr2:96557400-96656800	Weak transcription	Primary hematopoietic stem cells	blood
6	chr2:96574200-96629600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
7	chr2:96574600-96627600	Weak transcription	HSMM	muscle
8	chr2:96576800-96616200	Weak transcription	Brain Germinal Matrix	brain
9	chr2:96577800-96647800	Weak transcription	NHDF-Ad	bronchial
10	chr2:96577800-96651000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
11	chr2:96577800-96656600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
12	chr2:96578000-96645000	Weak transcription	NH-A	brain
13	chr2:96581400-96617000	Weak transcription	Pancreas	Pancrea
14	chr2:96582800-96656400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
15	chr2:96584000-96624600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
16	chr2:96584400-96621600	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
17	chr2:96585200-96649000	Weak transcription	Brain Inferior Temporal Lobe	brain
18	chr2:96585400-96616600	Weak transcription	Fetal Muscle Leg	muscle
19	chr2:96585600-96615400	Weak transcription	Fetal Muscle Trunk	muscle
20	chr2:96585600-96627400	Weak transcription	Left Ventricle	heart
21	chr2:96586000-96657200	Weak transcription	Ovary	ovary
22	chr2:96587800-96656600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
23	chr2:96588200-96649000	Weak transcription	Fetal Intestine Large	intestine
24	chr2:96589000-96616000	Weak transcription	Fetal Lung	lung
25	chr2:96589000-96631200	Weak transcription	Muscle Satellite Cultured Cells	--
26	chr2:96589000-96645400	Weak transcription	Skeletal Muscle Female	skeletal muscle
27	chr2:96591200-96616200	Weak transcription	Fetal Thymus	thymus
28	chr2:96593600-96616200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
29	chr2:96593600-96645000	Weak transcription	Adipose Nuclei	Adipose
30	chr2:96594400-96617600	Weak transcription	Primary T helper cells PMA-I stimulated	--
31	chr2:96594600-96623800	Weak transcription	Primary T cells fromperipheralblood	blood
32	chr2:96600600-96657200	Weak transcription	Duodenum Smooth Muscle	Duodenum
33	chr2:96600800-96617600	Weak transcription	Fetal Brain Male	brain
34	chr2:96600800-96621400	Weak transcription	A549	lung
35	chr2:96600800-96625600	Weak transcription	Rectal Mucosa Donor 29	rectum
36	chr2:96600800-96645000	Weak transcription	Primary T cells from cord blood	blood
37	chr2:96602600-96616000	Weak transcription	Fetal Brain Female	brain
38	chr2:96604200-96616800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
39	chr2:96604600-96616000	Weak transcription	Monocytes-CD14+_RO01746	blood
40	chr2:96605400-96644800	Weak transcription	Brain Anterior Caudate	brain
41	chr2:96605600-96655000	Weak transcription	HUVEC	blood vessel
42	chr2:96606000-96616200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
43	chr2:96606000-96635000	Weak transcription	Fetal Intestine Small	intestine
44	chr2:96606400-96657200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
45	chr2:96607400-96644600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
46	chr2:96607400-96657200	Weak transcription	Brain Hippocampus Middle	brain
47	chr2:96608400-96635000	Weak transcription	Thymus	Thymus
48	chr2:96609000-96616200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
49	chr2:96609000-96625800	Weak transcription	Rectal Mucosa Donor 31	rectum
50	chr2:96609200-96614400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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