Variant report

Variant	nsv215431
Chromosome Location	chr2:85860999-85866615
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	BCLAF1	chr2:85864540-85864976	GM12878	blood:	n/a	n/a
2	BHLHE40	chr2:85864670-85864880	K562	blood:	n/a	n/a
3	BRCA1	chr2:85864637-85864874	Hela-S3	cervix:	n/a	n/a
4	CEBPB	chr2:85861611-85861802	IMR90	lung:	n/a	n/a
5	CEBPB	chr2:85861610-85861702	A549	lung:	n/a	n/a
6	CEBPB	chr2:85864720-85864920	Hela-S3	cervix:	n/a	n/a
7	CTCF	chr2:85864720-85864870	AG04449	skin:	n/a	chr2:85864779-85864795 chr2:85864778-85864796 chr2:85864781-85864794 chr2:85864780-85864801 chr2:85864782-85864789
8	CTCF	chr2:85864681-85864871	ECC-1	luminal epithelium:	n/a	chr2:85864779-85864795 chr2:85864778-85864796 chr2:85864781-85864794 chr2:85864780-85864801 chr2:85864782-85864789
9	CTCF	chr2:85864700-85864850	GM12872	blood:	n/a	chr2:85864779-85864795 chr2:85864778-85864796 chr2:85864781-85864794 chr2:85864780-85864801 chr2:85864782-85864789
10	CTCF	chr2:85864700-85864850	GM12878	blood:	n/a	chr2:85864779-85864795 chr2:85864778-85864796 chr2:85864781-85864794 chr2:85864780-85864801 chr2:85864782-85864789
11	CTCF	chr2:85864621-85864976	MCF-7	breast:	n/a	chr2:85864779-85864795 chr2:85864778-85864796 chr2:85864781-85864794 chr2:85864780-85864801 chr2:85864782-85864789
12	CTCF	chr2:85864575-85865024	K562	blood:	n/a	chr2:85864779-85864795 chr2:85864778-85864796 chr2:85864781-85864794 chr2:85864780-85864801 chr2:85864782-85864789
13	CTCF	chr2:85864614-85865014	HepG2	liver:	n/a	chr2:85864779-85864795 chr2:85864778-85864796 chr2:85864781-85864794 chr2:85864780-85864801 chr2:85864782-85864789
14	CTCF	chr2:85864636-85864953	Fibrobl	skin:	n/a	chr2:85864779-85864795 chr2:85864778-85864796 chr2:85864781-85864794 chr2:85864780-85864801 chr2:85864782-85864789
15	CTCF	chr2:85864680-85864830	WI-38	lung:	n/a	chr2:85864779-85864795 chr2:85864778-85864796 chr2:85864781-85864794 chr2:85864780-85864801 chr2:85864782-85864789
16	CTCF	chr2:85864720-85864870	HFF-Myc	foreskin:	n/a	chr2:85864779-85864795 chr2:85864778-85864796 chr2:85864781-85864794 chr2:85864780-85864801 chr2:85864782-85864789
17	CTCF	chr2:85864720-85864870	BJ	skin:	n/a	chr2:85864779-85864795 chr2:85864778-85864796 chr2:85864781-85864794 chr2:85864780-85864801 chr2:85864782-85864789
18	CTCF	chr2:85864000-85864150	AoAF	blood vessel:	n/a	n/a
19	CTCF	chr2:85864805-85864928	H1-hESC	embryonic stem cell:	n/a	n/a
20	CTCF	chr2:85864669-85864978	MCF-7	breast:	n/a	chr2:85864779-85864795 chr2:85864778-85864796 chr2:85864781-85864794 chr2:85864780-85864801 chr2:85864782-85864789
21	CTCF	chr2:85864720-85864870	SAEC	small airway:	n/a	chr2:85864779-85864795 chr2:85864778-85864796 chr2:85864781-85864794 chr2:85864780-85864801 chr2:85864782-85864789
22	CTCF	chr2:85864637-85864923	Pancreas_OC	pancreas:	n/a	chr2:85864779-85864795 chr2:85864778-85864796 chr2:85864781-85864794 chr2:85864780-85864801 chr2:85864782-85864789
23	CTCF	chr2:85864575-85865031	MCF-7	breast:	n/a	chr2:85864779-85864795 chr2:85864778-85864796 chr2:85864781-85864794 chr2:85864780-85864801 chr2:85864782-85864789
24	CTCF	chr2:85864439-85865038	MCF-7	breast:	n/a	chr2:85864779-85864795 chr2:85864778-85864796 chr2:85864781-85864794 chr2:85864780-85864801 chr2:85864782-85864789
25	CTCF	chr2:85864680-85864830	HRE	kidney:	n/a	chr2:85864779-85864795 chr2:85864778-85864796 chr2:85864781-85864794 chr2:85864780-85864801 chr2:85864782-85864789
26	CTCF	chr2:85864600-85864750	HAc	cerebellar:	n/a	n/a
27	CTCF	chr2:85864660-85864810	GM12875	blood:	n/a	chr2:85864779-85864795 chr2:85864778-85864796 chr2:85864781-85864794 chr2:85864780-85864801 chr2:85864782-85864789
28	CTCF	chr2:85864700-85864850	GM12865	blood:	n/a	chr2:85864779-85864795 chr2:85864778-85864796 chr2:85864781-85864794 chr2:85864780-85864801 chr2:85864782-85864789
29	CTCF	chr2:85864652-85864926	GM19239	blood:	n/a	chr2:85864779-85864795 chr2:85864778-85864796 chr2:85864781-85864794 chr2:85864780-85864801 chr2:85864782-85864789
30	CTCF	chr2:85864680-85864964	MCF-7	breast:	n/a	chr2:85864779-85864795 chr2:85864778-85864796 chr2:85864781-85864794 chr2:85864780-85864801 chr2:85864782-85864789
31	CTCF	chr2:85864720-85864870	HepG2	liver:	n/a	chr2:85864779-85864795 chr2:85864778-85864796 chr2:85864781-85864794 chr2:85864780-85864801 chr2:85864782-85864789
32	CTCF	chr2:85864700-85864850	A549	lung:	n/a	chr2:85864779-85864795 chr2:85864778-85864796 chr2:85864781-85864794 chr2:85864780-85864801 chr2:85864782-85864789
33	CTCF	chr2:85864720-85864870	GM12801	blood:	n/a	chr2:85864779-85864795 chr2:85864778-85864796 chr2:85864781-85864794 chr2:85864780-85864801 chr2:85864782-85864789
34	CTCF	chr2:85864542-85864947	K562	blood:	n/a	chr2:85864779-85864795 chr2:85864778-85864796 chr2:85864781-85864794 chr2:85864780-85864801 chr2:85864782-85864789
35	CTCF	chr2:85864760-85864910	GM12869	blood:	n/a	chr2:85864779-85864795 chr2:85864778-85864796 chr2:85864781-85864794 chr2:85864780-85864801 chr2:85864782-85864789
36	CTCF	chr2:85864720-85864870	HUVEC	blood vessel:	n/a	chr2:85864779-85864795 chr2:85864778-85864796 chr2:85864781-85864794 chr2:85864780-85864801 chr2:85864782-85864789
37	CTCF	chr2:85864380-85864530	AG09309	skin:	n/a	n/a
38	CTCF	chr2:85864720-85864870	WERI-Rb-1	eye:	n/a	chr2:85864779-85864795 chr2:85864778-85864796 chr2:85864781-85864794 chr2:85864780-85864801 chr2:85864782-85864789
39	CTCF	chr2:85864280-85864430	HCM	heart:	n/a	n/a
40	CTCF	chr2:85864614-85864931	SK-N-SH_RA	brain:	n/a	chr2:85864779-85864795 chr2:85864778-85864796 chr2:85864781-85864794 chr2:85864780-85864801 chr2:85864782-85864789
41	CTCF	chr2:85864637-85864919	NHEK	skin:	n/a	chr2:85864779-85864795 chr2:85864778-85864796 chr2:85864781-85864794 chr2:85864780-85864801 chr2:85864782-85864789
42	CTCF	chr2:85864628-85864949	HepG2	liver:	n/a	chr2:85864779-85864795 chr2:85864778-85864796 chr2:85864781-85864794 chr2:85864780-85864801 chr2:85864782-85864789
43	CTCF	chr2:85864720-85864870	Caco-2	colon:	n/a	chr2:85864779-85864795 chr2:85864778-85864796 chr2:85864781-85864794 chr2:85864780-85864801 chr2:85864782-85864789
44	CTCF	chr2:85864637-85864904	SK-N-SH_RA	brain:	n/a	chr2:85864779-85864795 chr2:85864778-85864796 chr2:85864781-85864794 chr2:85864780-85864801 chr2:85864782-85864789
45	CTCF	chr2:85864654-85864958	Lung_OC	lung:	n/a	chr2:85864779-85864795 chr2:85864778-85864796 chr2:85864781-85864794 chr2:85864780-85864801 chr2:85864782-85864789
46	CTCF	chr2:85864720-85864870	AG10803	skin:	n/a	chr2:85864779-85864795 chr2:85864778-85864796 chr2:85864781-85864794 chr2:85864780-85864801 chr2:85864782-85864789
47	CTCF	chr2:85864720-85864870	GM12865	blood:	n/a	chr2:85864779-85864795 chr2:85864778-85864796 chr2:85864781-85864794 chr2:85864780-85864801 chr2:85864782-85864789
48	CTCF	chr2:85864040-85864190	GM12873	blood:	n/a	n/a
49	CTCF	chr2:85864537-85865067	A549	lung:	n/a	chr2:85864779-85864795 chr2:85864778-85864796 chr2:85864781-85864794 chr2:85864780-85864801 chr2:85864782-85864789
50	CTCF	chr2:85864720-85864870	GM12874	blood:	n/a	chr2:85864779-85864795 chr2:85864778-85864796 chr2:85864781-85864794 chr2:85864780-85864801 chr2:85864782-85864789

No.	Distal block	Cell Line	Cell type
1	chr2:85845054..85846904-chr2:85859258..85861801,2	MCF-7	breast:
2	chr2:85837890..85840693-chr2:85862564..85864246,2	K562	blood:
3	chr2:85646486..85648346-chr2:85864156..85866210,2	MCF-7	breast:
4	chr2:85828725..85830430-chr2:85863230..85865489,2	MCF-7	breast:
5	chr2:85804448..85806570-chr2:85864637..85866204,2	MCF-7	breast:
6	chr2:85864326..85865205-chr2:86031487..86032048,2	K562	blood:
7	chr2:85765276..85767700-chr2:85863355..85867135,3	MCF-7	breast:
8	chr2:85863255..85866624-chr2:85867202..85869540,4	K562	blood:
9	chr2:85864268..85866624-chr2:85868016..85871094,4	K562	blood:
10	chr2:85855008..85857612-chr2:85860725..85862403,3	MCF-7	breast:
11	chr2:85860109..85864294-chr2:85864823..85868002,4	K562	blood:
12	chr2:85766440..85769334-chr2:85864127..85866072,2	K562	blood:
13	chr2:85864338..85865140-chr2:85944938..85945570,2	K562	blood:
14	chr2:85860109..85864294-chr2:85864823..85868002,4	K562	blood:

Variant related genes	Relation type
USP39	TF binding region
ENSG00000168887	chromatin interactions
ENSG00000168883	chromatin interactions
ENSG00000152292	chromatin interactions
ENSG00000168906	chromatin interactions
ENSG00000118640	chromatin interactions
ENSG00000168890	chromatin interactions

Extended variants
information (count: 246 )
Associated
traits (count: 49 )

Variant overlapped rSNPs/rCNVs (count:246 , 50 per page) page: 1 2 3 4 5

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7594258	chr2:85860999-85861000	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs62166777	chr2:85861007-85861008	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs549178003	chr2:85861030-85861031	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs375969166	chr2:85861053-85861054	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs535704324	chr2:85861106-85861107	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs7609380	chr2:85861142-85861143	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs561446848	chr2:85861161-85861162	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs529059356	chr2:85861166-85861167	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs185592069	chr2:85861179-85861180	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs565637092	chr2:85861182-85861183	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs112619517	chr2:85861204-85861205	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs191578293	chr2:85861207-85861208	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs569264252	chr2:85861236-85861237	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs371281884	chr2:85861253-85861254	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs112178272	chr2:85861256-85861257	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs567389366	chr2:85861289-85861290	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs115235685	chr2:85861325-85861326	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs566071791	chr2:85861351-85861352	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs116635400	chr2:85861379-85861380	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs557761921	chr2:85861421-85861422	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs375424295	chr2:85861437-85861438	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs545668804	chr2:85861438-85861439	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs146742240	chr2:85861462-85861463	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs575673516	chr2:85861477-85861478	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs140454238	chr2:85861531-85861532	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs144092800	chr2:85861554-85861555	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs373300624	chr2:85861569-85861570	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs537162822	chr2:85861570-85861571	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs146497594	chr2:85861574-85861575	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs62166778	chr2:85861630-85861631	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs183831222	chr2:85861688-85861689	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs532965372	chr2:85861689-85861690	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs549048172	chr2:85861696-85861697	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs569631517	chr2:85861698-85861699	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs116224920	chr2:85861754-85861755	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs548991723	chr2:85861800-85861801	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs72923062	chr2:85861829-85861830	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs541270220	chr2:85861844-85861845	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs534674128	chr2:85861890-85861891	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs140767319	chr2:85861950-85861951	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs577899331	chr2:85861954-85861955	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs72923064	chr2:85862052-85862053	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs188580881	chr2:85862131-85862132	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs557669064	chr2:85862138-85862139	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs575919764	chr2:85862174-85862175	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs542655021	chr2:85862186-85862187	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs150107410	chr2:85862211-85862212	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs573168031	chr2:85862231-85862232	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs531197950	chr2:85862252-85862253	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs72923066	chr2:85862275-85862276	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:49)

Disease	PMID	Source
Chronic lymphocytic leukemia	21546498	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
Follicular lymphoma	20505157	CNVD
Autism	17483303	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Medulloblastoma	20607354	CNVD
Autism	22495311	CNVD
Autism	18522746	CNVD
Neurodevelopmental disorder	22521361	CNVD
Lung cancer	18438408	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
small cell lung cancer	20016488	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	16272173	CNVD
Breast cancer	20409316	CNVD
Breast cancer	21990379	CNVD
Astrocytoma	22246337	CNVD
Papillary thyroid carcinoma	22161024	CNVD
Myelofibrosis	22110671	CNVD
Schizophrenia	21399695	CNVD
Breast cancer	21364760	CNVD
Glioblastoma multiforme	19115005	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:248 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:85843800-85876000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
2	chr2:85844800-85862600	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
3	chr2:85844800-85881600	Strong transcription	HUES48 Cell Line	embryonic stem cell
4	chr2:85845000-85876000	Weak transcription	Right Atrium	heart
5	chr2:85845000-85879800	Strong transcription	iPS-18 Cell Line	embryonic stem cell
6	chr2:85845000-85880000	Strong transcription	iPS-20b Cell Line	embryonic stem cell
7	chr2:85845000-85880800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
8	chr2:85845000-85881400	Strong transcription	HUES6 Cell Line	embryonic stem cell
9	chr2:85845000-85881800	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
10	chr2:85845000-85883600	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
11	chr2:85845400-85864600	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
12	chr2:85845400-85879800	Strong transcription	Lung	lung
13	chr2:85845400-85881000	Strong transcription	Primary hematopoietic stem cells short term culture	blood
14	chr2:85845400-85881400	Strong transcription	Breast Myoepithelial Primary Cells	Breast
15	chr2:85845400-85886400	Strong transcription	Fetal Muscle Leg	muscle
16	chr2:85845600-85881800	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
17	chr2:85845600-85882200	Strong transcription	Fetal Muscle Trunk	muscle
18	chr2:85845800-85865000	Strong transcription	NH-A	brain
19	chr2:85845800-85881400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
20	chr2:85845800-85881600	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
21	chr2:85845800-85881800	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
22	chr2:85846000-85875600	Strong transcription	Primary hematopoietic stem cells	blood
23	chr2:85846000-85880800	Strong transcription	Sigmoid Colon	Sigmoid Colon
24	chr2:85846000-85881400	Strong transcription	Fetal Stomach	stomach
25	chr2:85846000-85881400	Strong transcription	Fetal Thymus	thymus
26	chr2:85846000-85887000	Strong transcription	Liver	Liver
27	chr2:85846000-85887400	Strong transcription	Fetal Intestine Small	intestine
28	chr2:85846200-85864200	Strong transcription	Brain Germinal Matrix	brain
29	chr2:85846200-85871600	Strong transcription	Skeletal Muscle Male	skeletal muscle
30	chr2:85846200-85874600	Strong transcription	Primary monocytes fromperipheralblood	blood
31	chr2:85846200-85874600	Strong transcription	Monocytes-CD14+_RO01746	blood
32	chr2:85846200-85875000	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
33	chr2:85846200-85875200	Strong transcription	Placenta	Placenta
34	chr2:85846200-85879400	Strong transcription	Cortex derived primary cultured neurospheres	brain
35	chr2:85846200-85879400	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
36	chr2:85846200-85880000	Strong transcription	HUES64 Cell Line	embryonic stem cell
37	chr2:85846200-85880000	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
38	chr2:85846200-85880000	Strong transcription	Stomach Smooth Muscle	stomach
39	chr2:85846200-85880600	Strong transcription	H1 Cell Line	embryonic stem cell
40	chr2:85846200-85881200	Strong transcription	Primary neutrophils fromperipheralblood	blood
41	chr2:85846200-85881400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
42	chr2:85846200-85881400	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
43	chr2:85846200-85882000	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
44	chr2:85846200-85889400	Strong transcription	Thymus	Thymus
45	chr2:85846400-85864600	Strong transcription	Primary T cells fromperipheralblood	blood
46	chr2:85846400-85864800	Strong transcription	Primary B cells from cord blood	blood
47	chr2:85846400-85869200	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
48	chr2:85846400-85879600	Strong transcription	Fetal Intestine Large	intestine
49	chr2:85846400-85880600	Strong transcription	H9 Cell Line	embryonic stem cell
50	chr2:85846600-85861600	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin

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