Variant report

Variant	nsv2778
Chromosome Location	chr2:73596272-73615138
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:709)
CpG islands
(count:794)
Chromatin interactive
region (count:24)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:709 , 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	chr2:73612269-73612787	HepG2	liver:	n/a	n/a
2	ATF1	chr2:73595903-73596308	K562	blood:	n/a	n/a
3	ATF3	chr2:73613299-73613512	K562	blood:	n/a	chr2:73613391-73613411
4	BACH1	chr2:73612687-73612801	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr2:73613214-73613488	H1-hESC	embryonic stem cell:	n/a	n/a
6	BCLAF1	chr2:73612999-73613606	GM12878	blood:	n/a	chr2:73613474-73613487
7	BCLAF1	chr2:73612475-73612934	GM12878	blood:	n/a	n/a
8	BCLAF1	chr2:73613068-73613624	GM12878	blood:	n/a	chr2:73613474-73613487
9	BHLHE40	chr2:73613882-73613924	K562	blood:	n/a	n/a
10	BHLHE40	chr2:73612356-73613588	GM12878	blood:	n/a	chr2:73613468-73613484
11	BHLHE40	chr2:73612356-73613640	K562	blood:	n/a	chr2:73613468-73613484
12	BRCA1	chr2:73613504-73613637	GM12878	blood:	n/a	n/a
13	BRCA1	chr2:73612613-73612855	H1-hESC	embryonic stem cell:	n/a	n/a
14	BRCA1	chr2:73612380-73613740	Hela-S3	cervix:	n/a	n/a
15	BRCA1	chr2:73612527-73612693	HepG2	liver:	n/a	n/a
16	CBX3	chr2:73612575-73613612	K562	blood:	n/a	n/a
17	CCNT2	chr2:73612619-73613655	K562	blood:	n/a	n/a
18	CEBPB	chr2:73595897-73596293	K562	blood:	n/a	n/a
19	CEBPB	chr2:73601577-73601752	HepG2	liver:	n/a	chr2:73601590-73601601
20	CEBPB	chr2:73598725-73598880	A549	lung:	n/a	n/a
21	CEBPB	chr2:73601518-73601590	IMR90	lung:	n/a	n/a
22	CEBPB	chr2:73612635-73612993	Hela-S3	cervix:	n/a	n/a
23	CEBPB	chr2:73595878-73596295	K562	blood:	n/a	n/a
24	CEBPD	chr2:73595870-73596334	K562	blood:	n/a	n/a
25	CEBPD	chr2:73613189-73613518	HepG2	liver:	n/a	n/a
26	CEBPD	chr2:73612954-73613186	HepG2	liver:	n/a	n/a
27	CHD1	chr2:73613854-73614182	H1-hESC	embryonic stem cell:	n/a	n/a
28	CHD1	chr2:73613115-73613651	H1-hESC	embryonic stem cell:	n/a	n/a
29	CHD1	chr2:73613195-73613673	GM12878	blood:	n/a	n/a
30	CHD2	chr2:73612387-73613725	GM12878	blood:	n/a	chr2:73612779-73612789
31	CHD2	chr2:73612655-73613577	HepG2	liver:	n/a	chr2:73612779-73612789
32	CHD2	chr2:73612647-73612887	H1-hESC	embryonic stem cell:	n/a	chr2:73612779-73612789
33	CHD2	chr2:73612569-73613587	K562	blood:	n/a	chr2:73612779-73612789
34	CHD2	chr2:73613500-73613519	H1-hESC	embryonic stem cell:	n/a	n/a
35	CHD2	chr2:73612546-73613562	Hela-S3	cervix:	n/a	chr2:73612779-73612789
36	CHD2	chr2:73613847-73613877	K562	blood:	n/a	n/a
37	CHD2	chr2:73613127-73613153	H1-hESC	embryonic stem cell:	n/a	n/a
38	CREB1	chr2:73612531-73613711	GM12878	blood:	n/a	n/a
39	CREB1	chr2:73613339-73613610	A549	lung:	n/a	n/a
40	CREB1	chr2:73612585-73613685	K562	blood:	n/a	n/a
41	CREB1	chr2:73612936-73613216	A549	lung:	n/a	n/a
42	CREB1	chr2:73612531-73613891	A549	lung:	n/a	n/a
43	CREB1	chr2:73612552-73613523	H1-hESC	embryonic stem cell:	n/a	n/a
44	CREB1	chr2:73612375-73613792	HepG2	liver:	n/a	n/a
45	CREB1	chr2:73612552-73613986	HepG2	liver:	n/a	n/a
46	CTCF	chr2:73613320-73613470	GM12873	blood:	n/a	n/a
47	CTCF	chr2:73613360-73613369	Kidney_OC	kidney:	n/a	n/a
48	CTCF	chr2:73613359-73613498	MCF-7	breast:	n/a	n/a
49	CTCF	chr2:73613320-73613470	GM12871	blood:	n/a	n/a
50	CTCF	chr2:73613380-73613530	HRE	kidney:	n/a	n/a

(count:794 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:73612707-73612757	K562	blood:	n/a
2	chr2:73612707-73612757	K562	blood:	n/a
3	chr2:73612302-73612352	HEEpiC	esophagus:	n/a
4	chr2:73612788-73612838	ProgFib	skin:	n/a
5	chr2:73612757-73612807	NH-A	brain:	n/a
6	chr2:73613564-73613614	HCF	heart:	n/a
7	chr2:73612889-73612939	BE2_C	brain:	n/a
8	chr2:73612302-73612352	AG09319	gingival:	n/a
9	chr2:73612712-73612762	Caco-2	colon:	n/a
10	chr2:73612656-73612706	IMR90	lung:	fetal
11	chr2:73612707-73612757	NHDF-neo	bronchial:	n/a
12	chr2:73612788-73612838	LNCaP	prostate:	n/a
13	chr2:73612893-73612943	HCF	heart:	n/a
14	chr2:73612889-73612939	HEK293	kidney:	embryo
15	chr2:73612889-73612939	HNPCEpiC	eye:	n/a
16	chr2:73612788-73612838	AG09309	skin:	n/a
17	chr2:73612893-73612943	HIPEpiC	eye:	n/a
18	chr2:73613564-73613614	AG10803	skin:	n/a
19	chr2:73612302-73612352	AG04450	lung:	fetal
20	chr2:73613845-73613895	HCT-116	colon:	n/a
21	chr2:73612673-73612723	AG10803	skin:	n/a
22	chr2:73612656-73612706	Caco-2	colon:	n/a
23	chr2:73612889-73612939	RPTEC	kidney:	n/a
24	chr2:73608838-73608888	AoSMC	blood vessel:	n/a
25	chr2:73612302-73612352	HRCEpiC	kidney:	n/a
26	chr2:73612656-73612706	SAEC	small airway:	n/a
27	chr2:73613564-73613614	PrEC	prostate:	n/a
28	chr2:73612302-73612352	HCT-116	colon:	n/a
29	chr2:73612712-73612762	AoSMC	blood vessel:	n/a
30	chr2:73612302-73612352	SK-N-SH_RA	brain:	n/a
31	chr2:73613845-73613895	GM12892	blood:	n/a
32	chr2:73608838-73608888	MCF10A-Er-Src	breast:	n/a
33	chr2:73612656-73612706	SKMC	muscle:	n/a
34	chr2:73612673-73612723	HAEpiC	amniotic membrane:	n/a
35	chr2:73613587-73613637	SK-N-MC	brain:	n/a
36	chr2:73613564-73613614	HAEpiC	amniotic membrane:	n/a
37	chr2:73612757-73612807	GM12878	blood:	n/a
38	chr2:73612712-73612762	HL-60	blood:	n/a
39	chr2:73612889-73612939	H1-hESC	embryonic stem cell:	embryo
40	chr2:73612707-73612757	AG10803	skin:	n/a
41	chr2:73612302-73612352	SK-N-MC	brain:	n/a
42	chr2:73612673-73612723	GM12891	blood:	n/a
43	chr2:73612656-73612706	U87	brain:	n/a
44	chr2:73612656-73612706	T-47D	breast:	n/a
45	chr2:73612302-73612352	GM12891	blood:	n/a
46	chr2:73612302-73612352	GM12892	blood:	n/a
47	chr2:73612893-73612943	HRPEpiC	eye:	n/a
48	chr2:73612302-73612352	AG10803	skin:	n/a
49	chr2:73612302-73612352	MCF-7	breast:	n/a
50	chr2:73612673-73612723	HMEC	breast:	n/a

(count:24 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:198125724..198126412-chr2:73612666..73613508,2	Hela-S3	cervix:
2	chr2:73590790..73592935-chr2:73594185..73596507,2	K562	blood:
3	chr2:73494646..73496647-chr2:73610262..73612844,2	MCF-7	breast:
4	chr2:73603553..73605160-chr2:73611586..73613395,2	MCF-7	breast:
5	chr19:49121875..49122578-chr2:73612539..73613302,2	Hela-S3	cervix:
6	chr2:73612640..73613510-chr9:100684147..100685046,2	Hela-S3	cervix:
7	chr2:73605670..73609629-chr2:73611404..73613842,4	K562	blood:
8	chr2:73612210..73615081-chr2:73714696..73716979,2	MCF-7	breast:
9	chr2:73511465..73512045-chr2:73612502..73613373,2	K562	blood:
10	chr1:153508450..153509207-chr2:73613075..73613614,2	Hela-S3	cervix:
11	chr2:73460503..73462797-chr2:73611325..73612830,2	MCF-7	breast:
12	chr10:103911747..103912466-chr2:73612539..73613400,2	Hela-S3	cervix:
13	chr2:73597000..73599124-chr2:73599512..73601523,2	K562	blood:
14	chr2:73605602..73610192-chr2:73611523..73615241,7	K562	blood:
15	chr2:73613233..73615069-chr2:73661651..73663882,2	MCF-7	breast:
16	chr2:73605402..73609183-chr2:73611183..73613614,6	MCF-7	breast:
17	chr2:73590985..73593218-chr2:73601136..73602952,2	MCF-7	breast:
18	chr2:73596191..73598481-chr2:73612504..73614239,2	K562	blood:
19	chr2:73550358..73552721-chr2:73600201..73602328,2	MCF-7	breast:
20	chr2:73497659..73500414-chr2:73612511..73614881,2	MCF-7	breast:
21	chr2:73596191..73598481-chr2:73612504..73614239,2	K562	blood:
22	chr2:73460084..73462978-chr2:73611729..73614401,3	K562	blood:
23	chr2:73606604..73608316-chr2:73620841..73623295,2	K562	blood:
24	chr2:73597856..73600814-chr2:73611443..73614137,4	MCF-7	breast:

No data

Variant related genes	Relation type
ALMS1	TF binding region
ENSG00000214484	TF binding region
ALMS1	CpG island
ENSG00000214484	CpG island
ENSG00000135624	chromatin interactions
ENSG00000166197	chromatin interactions
ENSG00000116127	chromatin interactions
ENSG00000135617	chromatin interactions
ENSG00000063177	chromatin interactions
ENSG00000197956	chromatin interactions
ENSG00000151414	chromatin interactions
ENSG00000063176	chromatin interactions
ENSG00000221087	chromatin interactions
ENSG00000214484	chromatin interactions
ENSG00000163013	chromatin interactions
ENSG00000136932	chromatin interactions

Extended variants
information (count: 520 )
Associated
traits (count: 52 )

Variant overlapped rSNPs/rCNVs (count:520 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs55924008	chr2:73596290-73596291	Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs570981822	chr2:73596357-73596358	Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs554514219	chr2:73596439-73596440	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs187021576	chr2:73596521-73596522	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs151145873	chr2:73596547-73596548	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs367978374	chr2:73596571-73596572	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs370745847	chr2:73596582-73596583	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs553967435	chr2:73596583-73596584	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs111722105	chr2:73596594-73596595	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs191860109	chr2:73596597-73596598	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs376661430	chr2:73596602-73596603	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs7567343	chr2:73596605-73596606	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
13	rs140058858	chr2:73596633-73596634	Inactive region	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs543036164	chr2:73596678-73596679	Inactive region	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs532036428	chr2:73596689-73596690	Inactive region	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs183943771	chr2:73596715-73596716	Inactive region	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs532107912	chr2:73596749-73596750	Inactive region	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs540745535	chr2:73596751-73596752	Inactive region	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs550255942	chr2:73596753-73596754	Inactive region	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs10184301	chr2:73596765-73596766	Inactive region	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs188300474	chr2:73596832-73596833	Inactive region	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs11126398	chr2:73596951-73596952	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs77231634	chr2:73596972-73596973	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs531205706	chr2:73596990-73596991	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs552619521	chr2:73597018-73597019	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs2901437	chr2:73597024-73597025	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
27	rs535151883	chr2:73597057-73597058	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs572664384	chr2:73597142-73597143	Inactive region	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs185647361	chr2:73597157-73597158	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs568500589	chr2:73597165-73597166	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs536059485	chr2:73597175-73597176	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs554720336	chr2:73597177-73597178	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs575946240	chr2:73597210-73597211	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs545438484	chr2:73597211-73597212	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs558156388	chr2:73597217-73597218	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs576424933	chr2:73597244-73597245	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs541160045	chr2:73597262-73597263	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs559194045	chr2:73597303-73597304	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs574429769	chr2:73597305-73597306	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs558901535	chr2:73597332-73597333	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs190505285	chr2:73597345-73597346	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs531266289	chr2:73597371-73597372	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs116727109	chr2:73597467-73597468	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs534079428	chr2:73597474-73597475	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs564519179	chr2:73597488-73597489	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs371433983	chr2:73597489-73597490	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs528487176	chr2:73597501-73597502	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs181754317	chr2:73597504-73597505	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs568481966	chr2:73597505-73597506	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs535908552	chr2:73597526-73597527	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:52)

Disease	PMID	Source
Chronic lymphocytic leukemia	21546498	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17387387	CNVD
Neuroblastoma	17533364	CNVD
Neuroblastoma	18923191	CNVD
Endometrial cancer	22040021	CNVD
Adrenal tumor	17535989	CNVD
Breast cancer	21264507	CNVD
Basal cell lymphoma	17053054	CNVD
Medulloblastoma	17522785	CNVD
Cancer	23418310	CNVD
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
Hodgkin''s lymphoma	18641027	CNVD
Follicular lymphoma	20505157	CNVD
Autism	17483303	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Medulloblastoma	20607354	CNVD
Autism	22495311	CNVD
Autism	18522746	CNVD
Lung cancer	18438408	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
Developmental delay	21147756	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Seminomas	18059402	CNVD
Testicular germ cell tumor	18059402	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Hepatocellular carcinoma	16750200	CNVD
Renal cell carcinoma	18765545	CNVD
Myxofibrosarcoma	16751306	CNVD
small cell lung cancer	20016488	CNVD
Acute myeloid leukemia	21251322	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:511 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:73595800-73596600	Enhancers	K562	blood
2	chr2:73597600-73598000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr2:73600600-73600800	Enhancers	K562	blood
4	chr2:73600600-73601000	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
5	chr2:73609000-73610000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
6	chr2:73610000-73612000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
7	chr2:73610400-73610800	Bivalent Enhancer	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
8	chr2:73610400-73610800	Bivalent Enhancer	HepG2	liver
9	chr2:73610600-73610800	Bivalent Enhancer	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
10	chr2:73610800-73611400	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
11	chr2:73611400-73611800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
12	chr2:73611600-73612000	Enhancers	Dnd41	blood
13	chr2:73611600-73612000	Bivalent Enhancer	HepG2	liver
14	chr2:73611600-73612000	Enhancers	K562	blood
15	chr2:73611600-73612200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
16	chr2:73611600-73612200	Enhancers	Fetal Intestine Small	intestine
17	chr2:73611800-73612000	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
18	chr2:73612000-73612200	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
19	chr2:73612000-73612200	Flanking Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
20	chr2:73612000-73612200	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
21	chr2:73612000-73612200	Active TSS	HUES6 Cell Line	embryonic stem cell
22	chr2:73612000-73612200	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
23	chr2:73612000-73612200	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
24	chr2:73612000-73612200	Enhancers	Breast Myoepithelial Primary Cells	Breast
25	chr2:73612000-73612200	Enhancers	Primary T cells from cord blood	blood
26	chr2:73612000-73612200	Enhancers	Primary hematopoietic stem cells short term culture	blood
27	chr2:73612000-73612200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
28	chr2:73612000-73612200	Enhancers	Primary T helper naive cells from peripheral blood	blood
29	chr2:73612000-73612200	Enhancers	Primary T helper naive cells fromperipheralblood	blood
30	chr2:73612000-73612200	Enhancers	Primary T helper cells PMA-I stimulated	--
31	chr2:73612000-73612200	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
32	chr2:73612000-73612200	Enhancers	Primary T helper cells fromperipheralblood	blood
33	chr2:73612000-73612200	Enhancers	Primary T killer memory cells from peripheral blood	blood
34	chr2:73612000-73612200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
35	chr2:73612000-73612200	Enhancers	Muscle Satellite Cultured Cells	--
36	chr2:73612000-73612200	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
37	chr2:73612000-73612200	Enhancers	Adipose Nuclei	Adipose
38	chr2:73612000-73612200	Enhancers	Liver	Liver
39	chr2:73612000-73612200	Enhancers	Brain Angular Gyrus	brain
40	chr2:73612000-73612200	Enhancers	Brain Anterior Caudate	brain
41	chr2:73612000-73612200	Flanking Active TSS	Brain Cingulate Gyrus	brain
42	chr2:73612000-73612200	Enhancers	Brain Hippocampus Middle	brain
43	chr2:73612000-73612200	Enhancers	Brain Inferior Temporal Lobe	brain
44	chr2:73612000-73612200	Enhancers	Brain Substantia Nigra	brain
45	chr2:73612000-73612200	Enhancers	Duodenum Mucosa	Duodenum
46	chr2:73612000-73612200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
47	chr2:73612000-73612200	Enhancers	Fetal Heart	heart
48	chr2:73612000-73612200	Enhancers	Fetal Intestine Large	intestine
49	chr2:73612000-73612200	Enhancers	Pancreatic Islets	Pancreatic Islet
50	chr2:73612000-73612200	Enhancers	Fetal Lung	lung

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