Variant report

Variant	esv3325388
Chromosome Location	chr2:97559400-97561723
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:134)
CpG islands
(count:61)
Chromatin interactive
region (count:10)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:134 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:97560767-97561191	K562	blood:	n/a	n/a
2	BHLHE40	chr2:97560766-97561389	K562	blood:	n/a	n/a
3	BHLHE40	chr2:97559703-97559928	K562	blood:	n/a	n/a
4	CBX3	chr2:97560740-97561220	K562	blood:	n/a	n/a
5	CBX3	chr2:97560634-97561364	K562	blood:	n/a	n/a
6	CCNT2	chr2:97560755-97561372	K562	blood:	n/a	chr2:97561146-97561155
7	CCNT2	chr2:97559054-97559855	K562	blood:	n/a	n/a
8	CEBPB	chr2:97560778-97561237	K562	blood:	n/a	n/a
9	CEBPB	chr2:97560736-97561181	K562	blood:	n/a	n/a
10	CEBPB	chr2:97561525-97561685	K562	blood:	n/a	n/a
11	CEBPD	chr2:97560672-97561287	K562	blood:	n/a	n/a
12	CEBPD	chr2:97560641-97561296	K562	blood:	n/a	n/a
13	CHD2	chr2:97560725-97561535	K562	blood:	n/a	n/a
14	CTCF	chr2:97560677-97560886	T-47D	breast:	n/a	n/a
15	CTCF	chr2:97559380-97559530	WERI-Rb-1	eye:	n/a	n/a
16	CUX1	chr2:97559761-97559851	K562	blood:	n/a	n/a
17	CUX1	chr2:97560761-97561267	K562	blood:	n/a	n/a
18	E2F6	chr2:97560662-97561585	K562	blood:	n/a	chr2:97560863-97560874
19	E2F6	chr2:97560726-97560902	K562	blood:	n/a	chr2:97560863-97560874
20	E2F6	chr2:97560649-97561094	K562	blood:	n/a	chr2:97560863-97560874
21	E2F6	chr2:97560617-97561755	H1-hESC	embryonic stem cell:	n/a	chr2:97560863-97560874
22	E2F6	chr2:97561093-97561304	K562	blood:	n/a	n/a
23	EGR1	chr2:97560856-97561195	K562	blood:	n/a	n/a
24	EGR1	chr2:97559824-97560820	K562	blood:	n/a	n/a
25	EGR1	chr2:97559878-97560767	K562	blood:	n/a	n/a
26	ELK1	chr2:97559928-97560021	K562	blood:	n/a	n/a
27	EP300	chr2:97559558-97559826	T-47D	breast:	n/a	n/a
28	EP300	chr2:97560781-97561281	K562	blood:	n/a	n/a
29	EP300	chr2:97560675-97561645	K562	blood:	n/a	chr2:97561402-97561415
30	EP300	chr2:97560889-97561191	GM12878	blood:	n/a	n/a
31	FOS	chr2:97561253-97561736	MCF10A-Er-Src	breast:	n/a	chr2:97561556-97561565 chr2:97561555-97561565 chr2:97561555-97561564
32	FOS	chr2:97561129-97561726	MCF10A-Er-Src	breast:	n/a	chr2:97561556-97561565 chr2:97561555-97561565 chr2:97561555-97561564
33	FOS	chr2:97560974-97561112	MCF10A-Er-Src	breast:	n/a	n/a
34	FOS	chr2:97561392-97561725	MCF10A-Er-Src	breast:	n/a	chr2:97561556-97561565 chr2:97561555-97561565 chr2:97561555-97561564
35	FOS	chr2:97561407-97561722	MCF10A-Er-Src	breast:	n/a	chr2:97561556-97561565 chr2:97561555-97561565 chr2:97561555-97561564
36	FOSL1	chr2:97561369-97561645	K562	blood:	n/a	chr2:97561556-97561565 chr2:97561555-97561565 chr2:97561555-97561564
37	FOSL2	chr2:97561202-97561857	MCF-7	breast:	n/a	chr2:97561556-97561565 chr2:97561555-97561565 chr2:97561555-97561564
38	GATA1	chr2:97560619-97562368	K562	blood:	n/a	n/a
39	GATA1	chr2:97560650-97561599	PBDE	blood:	n/a	n/a
40	GATA2	chr2:97560715-97561222	K562	blood:	n/a	n/a
41	GATA2	chr2:97560709-97561273	K562	blood:	n/a	n/a
42	GATA2	chr2:97560683-97561252	K562	blood:	n/a	n/a
43	GATA3	chr2:97561184-97561981	MCF-7	breast:	n/a	n/a
44	GTF2F1	chr2:97560723-97561467	K562	blood:	n/a	n/a
45	HCFC1	chr2:97560841-97561299	K562	blood:	n/a	n/a
46	HDAC2	chr2:97560585-97560899	K562	blood:	n/a	n/a
47	HDAC2	chr2:97560936-97561616	K562	blood:	n/a	n/a
48	HEY1	chr2:97560613-97560944	K562	blood:	n/a	n/a
49	HMGN3	chr2:97560874-97561933	K562	blood:	n/a	chr2:97561554-97561563
50	HMGN3	chr2:97559400-97559580	K562	blood:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:97561669-97561719	PrEC	prostate:	n/a
2	chr2:97561669-97561719	NT2-D1	testis:	n/a
3	chr2:97561669-97561719	HRE	kidney:	n/a
4	chr2:97561669-97561719	ProgFib	skin:	n/a
5	chr2:97561669-97561719	MCF-7	breast:	n/a
6	chr2:97561669-97561719	Jurkat	blood:	n/a
7	chr2:97561669-97561719	SK-N-SH_RA	brain:	n/a
8	chr2:97561669-97561719	HCM	heart:	n/a
9	chr2:97561669-97561719	K562	blood:	n/a
10	chr2:97561669-97561719	SK-N-SH	brain:	n/a
11	chr2:97561669-97561719	PANC-1	pancreas:	n/a
12	chr2:97561669-97561719	GM06990	blood:	n/a
13	chr2:97561669-97561719	AG10803	skin:	n/a
14	chr2:97561669-97561719	SK-N-MC	brain:	n/a
15	chr2:97561669-97561719	GM19239	blood:	n/a
16	chr2:97561669-97561719	AG09319	gingival:	n/a
17	chr2:97561669-97561719	HEK293	kidney:	embryo
18	chr2:97561669-97561719	LNCaP	prostate:	n/a
19	chr2:97561669-97561719	BE2_C	brain:	n/a
20	chr2:97561669-97561719	CMK	blood:	n/a
21	chr2:97561669-97561719	Hepatocyte	liver:	n/a
22	chr2:97561669-97561719	HEEpiC	esophagus:	n/a
23	chr2:97561669-97561719	AG09309	skin:	n/a
24	chr2:97561669-97561719	U87	brain:	n/a
25	chr2:97561669-97561719	HCF	heart:	n/a
26	chr2:97561669-97561719	H1-hESC	embryonic stem cell:	embryo
27	chr2:97561669-97561719	HIPEpiC	eye:	n/a
28	chr2:97561669-97561719	HNPCEpiC	eye:	n/a
29	chr2:97561669-97561719	HPAEpiC	pulmonary alveolar:	n/a
30	chr2:97561669-97561719	HMEC	breast:	n/a
31	chr2:97561669-97561719	HRPEpiC	eye:	n/a
32	chr2:97561669-97561719	ovcar-3	ovarian:	n/a
33	chr2:97561669-97561719	HRCEpiC	kidney:	n/a
34	chr2:97561669-97561719	HCPEpiC	choroid plexus:	n/a
35	chr2:97561669-97561719	SAEC	small airway:	n/a
36	chr2:97561669-97561719	SKMC	muscle:	n/a
37	chr2:97561669-97561719	AG04449	skin:	fetal
38	chr2:97561669-97561719	HUVEC	blood vessel:	n/a
39	chr2:97561669-97561719	HepG2	liver:	n/a
40	chr2:97561669-97561719	GM12891	blood:	n/a
41	chr2:97561669-97561719	ECC-1	luminal epithelium:	n/a
42	chr2:97561669-97561719	T-47D	breast:	n/a
43	chr2:97561669-97561719	PFSK-1	brain:	n/a
44	chr2:97561669-97561719	RPTEC	kidney:	n/a
45	chr2:97561669-97561719	Hela-S3	cervix:	n/a
46	chr2:97561669-97561719	IMR90	lung:	fetal
47	chr2:97561669-97561719	GM12892	blood:	n/a
48	chr2:97561669-97561719	A549	lung:	n/a
49	chr2:97561669-97561719	NHDF-neo	bronchial:	n/a
50	chr2:97561669-97561719	AoSMC	blood vessel:	n/a

(count:10 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:97557941..97560811-chr2:97624763..97627667,2	MCF-7	breast:
2	chr2:97490386..97492773-chr2:97557628..97559451,2	MCF-7	breast:
3	chr2:97481114..97483138-chr2:97559703..97563563,4	MCF-7	breast:
4	chr2:97545881..97548014-chr2:97558703..97560346,2	K562	blood:
5	chr2:97530555..97533487-chr2:97558228..97559890,3	K562	blood:
6	chr2:97558219..97561795-chr2:97617145..97620359,3	K562	blood:
7	chr2:97530555..97532219-chr2:97558372..97559890,2	K562	blood:
8	chr2:97531702..97533612-chr2:97560749..97562713,2	K562	blood:
9	chr2:97557540..97561219-chr2:97615825..97618671,3	MCF-7	breast:
10	chr2:97522291..97526078-chr2:97561305..97564829,3	K562	blood:

No data

Variant related genes	Relation type
FAM178B	TF binding region
FAM178B	CpG island
ENSG00000168754	chromatin interactions
ENSG00000213337	chromatin interactions
ENSG00000163126	chromatin interactions
ENSG00000168758	chromatin interactions
ENSG00000168763	chromatin interactions

Extended variants
information (count: 87 )
Associated
traits (count: 52 )

Variant overlapped rSNPs/rCNVs (count:87 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs555276584	chr2:97559443-97559444	Weak transcription Enhancers Genic enhancers Bivalent Enhancer Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
2	rs548918543	chr2:97559451-97559452	Weak transcription Enhancers Genic enhancers Bivalent Enhancer Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs143178853	chr2:97559457-97559458	Weak transcription Enhancers Genic enhancers Bivalent Enhancer Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs534854920	chr2:97559464-97559465	Weak transcription Enhancers Genic enhancers Bivalent Enhancer Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs148310093	chr2:97559469-97559470	Weak transcription Enhancers Genic enhancers Bivalent Enhancer Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs141955998	chr2:97559471-97559472	Weak transcription Enhancers Genic enhancers Bivalent Enhancer Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs537064790	chr2:97559482-97559483	Weak transcription Enhancers Genic enhancers Bivalent Enhancer Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs146287890	chr2:97559483-97559484	Weak transcription Enhancers Genic enhancers Bivalent Enhancer Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs573997698	chr2:97559510-97559511	Weak transcription Enhancers Genic enhancers Bivalent Enhancer Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs35352216	chr2:97559550-97559551	Weak transcription Enhancers Genic enhancers Bivalent Enhancer Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs543295888	chr2:97559602-97559603	Weak transcription Enhancers Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs34913145	chr2:97559616-97559617	Weak transcription Enhancers Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs200012479	chr2:97559627-97559628	Weak transcription Enhancers Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs201571176	chr2:97559632-97559633	Weak transcription Enhancers Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs540801170	chr2:97559641-97559642	Weak transcription Enhancers Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs147523420	chr2:97559735-97559736	Weak transcription Enhancers Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs564185157	chr2:97559737-97559738	Weak transcription Enhancers Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs145520273	chr2:97559743-97559744	Weak transcription Enhancers Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs543442848	chr2:97559750-97559751	Weak transcription Enhancers Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs11677797	chr2:97559759-97559760	Weak transcription Enhancers Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs376034495	chr2:97559772-97559773	Weak transcription Enhancers Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs369630987	chr2:97559773-97559774	Weak transcription Enhancers Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs529247829	chr2:97559780-97559781	Weak transcription Enhancers Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs373884209	chr2:97559808-97559809	Weak transcription Enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs549259876	chr2:97559851-97559852	Weak transcription Enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs565767321	chr2:97559926-97559927	Weak transcription Enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs374140903	chr2:97559946-97559947	Weak transcription Enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs528275707	chr2:97559984-97559985	Weak transcription Enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs551253594	chr2:97560022-97560023	Weak transcription Enhancers Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs571430629	chr2:97560031-97560032	Weak transcription Enhancers Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs537100486	chr2:97560034-97560035	Weak transcription Enhancers Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs556976624	chr2:97560057-97560058	Weak transcription Enhancers Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs551229029	chr2:97560059-97560060	Weak transcription Enhancers Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs57675226	chr2:97560137-97560138	Weak transcription Enhancers Active TSS	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs111608917	chr2:97560157-97560158	Weak transcription Enhancers Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs186552734	chr2:97560164-97560165	Weak transcription Enhancers Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs150671924	chr2:97560230-97560231	Weak transcription Enhancers Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs553613273	chr2:97560234-97560235	Weak transcription Enhancers Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs139857959	chr2:97560263-97560264	Weak transcription Enhancers Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs191328602	chr2:97560402-97560403	Weak transcription Enhancers Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs57632006	chr2:97560450-97560451	Weak transcription Enhancers Active TSS	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs183843349	chr2:97560490-97560491	Weak transcription Enhancers Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	mRNA abundance
43	rs558098103	chr2:97560573-97560574	Weak transcription Enhancers Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs568482485	chr2:97560625-97560626	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs13421275	chr2:97560629-97560630	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs368042394	chr2:97560661-97560662	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs371962076	chr2:97560678-97560679	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs577818919	chr2:97560684-97560685	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs375861410	chr2:97560703-97560704	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs80341479	chr2:97560801-97560802	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	3 gene(s)	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
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
Breast cancer	22522925	CNVD

Chromatin state (count:213 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:97552600-97560800	Weak transcription	Hela-S3	cervix
2	chr2:97554200-97560800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
3	chr2:97554400-97561000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
4	chr2:97554400-97563400	Weak transcription	Cortex derived primary cultured neurospheres	brain
5	chr2:97554600-97563400	Weak transcription	Fetal Heart	heart
6	chr2:97554800-97561200	Weak transcription	Fetal Brain Female	brain
7	chr2:97555000-97560800	Weak transcription	Fetal Brain Male	brain
8	chr2:97555000-97561200	Weak transcription	Pancreas	Pancrea
9	chr2:97555600-97559800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
10	chr2:97555800-97559800	Enhancers	Primary T helper naive cells fromperipheralblood	blood
11	chr2:97556000-97559400	Enhancers	Lung	lung
12	chr2:97556000-97560000	Transcr. at gene 5' and 3'	K562	blood
13	chr2:97556000-97560200	Enhancers	Primary T helper cells fromperipheralblood	blood
14	chr2:97556000-97560200	Enhancers	Brain Hippocampus Middle	brain
15	chr2:97556000-97562200	Enhancers	Brain Anterior Caudate	brain
16	chr2:97556200-97559600	Enhancers	Primary T killer memory cells from peripheral blood	blood
17	chr2:97556200-97559800	Enhancers	Primary T helper cells PMA-I stimulated	--
18	chr2:97556200-97560000	Enhancers	Primary T cells fromperipheralblood	blood
19	chr2:97556200-97560000	Enhancers	Psoas Muscle	Psoas
20	chr2:97556200-97560200	Enhancers	Primary T cells from cord blood	blood
21	chr2:97556200-97560200	Enhancers	Brain Angular Gyrus	brain
22	chr2:97556200-97560200	Enhancers	Brain Substantia Nigra	brain
23	chr2:97556200-97562200	Enhancers	Brain Cingulate Gyrus	brain
24	chr2:97556200-97562400	Enhancers	Skeletal Muscle Female	skeletal muscle
25	chr2:97556400-97559400	Enhancers	Spleen	Spleen
26	chr2:97556400-97559800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
27	chr2:97556400-97560200	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
28	chr2:97556400-97565200	Enhancers	Breast Myoepithelial Primary Cells	Breast
29	chr2:97556600-97559400	Enhancers	Primary T helper naive cells from peripheral blood	blood
30	chr2:97556600-97566000	Enhancers	Fetal Thymus	thymus
31	chr2:97556800-97562600	Enhancers	Brain Inferior Temporal Lobe	brain
32	chr2:97557000-97561000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
33	chr2:97557200-97560000	Bivalent Enhancer	Fetal Muscle Trunk	muscle
34	chr2:97557200-97561200	Weak transcription	Thymus	Thymus
35	chr2:97557400-97560800	Weak transcription	HUES48 Cell Line	embryonic stem cell
36	chr2:97557400-97560800	Weak transcription	HUES64 Cell Line	embryonic stem cell
37	chr2:97557400-97561000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
38	chr2:97557400-97561000	Weak transcription	Duodenum Smooth Muscle	Duodenum
39	chr2:97557600-97560800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
40	chr2:97557600-97561000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
41	chr2:97557600-97561000	Weak transcription	Rectal Smooth Muscle	rectum
42	chr2:97557600-97561200	Weak transcription	H9 Cell Line	embryonic stem cell
43	chr2:97557600-97561200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
44	chr2:97557800-97560200	Enhancers	Placenta	Placenta
45	chr2:97557800-97560800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
46	chr2:97557800-97560800	Weak transcription	Small Intestine	intestine
47	chr2:97557800-97560800	Weak transcription	A549	lung
48	chr2:97557800-97561000	Weak transcription	Primary hematopoietic stem cells	blood
49	chr2:97557800-97561200	Weak transcription	H1 Cell Line	embryonic stem cell
50	chr2:97557800-97561200	Weak transcription	Gastric	stomach

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