Variant report

Variant	esv3323401
Chromosome Location	chr2:100935920-100940518
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:281)
CpG islands
(count:733)
Chromatin interactive
region (count:23)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:281 , 50 per page) page: 1 2 3 4 5 6

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr2:100937869-100938194	H1-hESC	embryonic stem cell:	n/a	n/a
2	BACH1	chr2:100938639-100939098	H1-hESC	embryonic stem cell:	n/a	n/a
3	BHLHE40	chr2:100938971-100939090	K562	blood:	n/a	chr2:100939035-100939051
4	BHLHE40	chr2:100937897-100938024	K562	blood:	n/a	n/a
5	CBX3	chr2:100937749-100938093	K562	blood:	n/a	n/a
6	CCNT2	chr2:100937796-100939124	K562	blood:	n/a	n/a
7	CEBPB	chr2:100937413-100937708	IMR90	lung:	n/a	n/a
8	CEBPB	chr2:100936592-100936792	K562	blood:	n/a	n/a
9	CEBPB	chr2:100938836-100938861	H1-hESC	embryonic stem cell:	n/a	n/a
10	CEBPB	chr2:100937398-100937733	H1-hESC	embryonic stem cell:	n/a	n/a
11	CEBPB	chr2:100937372-100937722	K562	blood:	n/a	n/a
12	CEBPB	chr2:100936567-100936755	HepG2	liver:	n/a	n/a
13	CEBPB	chr2:100937382-100937725	HepG2	liver:	n/a	n/a
14	CEBPB	chr2:100938866-100938977	K562	blood:	n/a	n/a
15	CHD2	chr2:100938845-100938960	K562	blood:	n/a	n/a
16	CREB1	chr2:100937804-100938081	A549	lung:	n/a	n/a
17	CTBP2	chr2:100938406-100939157	H1-hESC	embryonic stem cell:	n/a	n/a
18	CTBP2	chr2:100937494-100938186	H1-hESC	embryonic stem cell:	n/a	n/a
19	CTCF	chr2:100937700-100937850	RPTEC	kidney:	n/a	n/a
20	CTCF	chr2:100937880-100938030	RPTEC	kidney:	n/a	n/a
21	CTCF	chr2:100937803-100938045	MCF-7	breast:	n/a	n/a
22	CTCF	chr2:100937840-100937990	HBMEC	blood vessel:	n/a	n/a
23	CTCF	chr2:100937800-100937950	HFF-Myc	foreskin:	n/a	n/a
24	CTCF	chr2:100937820-100937970	HRPEpiC	eye:	n/a	n/a
25	CTCF	chr2:100938639-100938652	MCF-7	breast:	n/a	n/a
26	CTCF	chr2:100937820-100937970	AG09319	gingival:	n/a	n/a
27	CTCF	chr2:100937619-100938237	K562	blood:	n/a	n/a
28	CTCF	chr2:100937798-100938068	MCF-7	breast:	n/a	n/a
29	CTCF	chr2:100938890-100938978	A549	lung:	n/a	n/a
30	CTCF	chr2:100937860-100938010	HUVEC	blood vessel:	n/a	n/a
31	CTCF	chr2:100937820-100937970	HCFaa	heart:	n/a	n/a
32	CTCF	chr2:100937900-100938050	GM12871	blood:	n/a	n/a
33	CTCF	chr2:100937730-100938100	K562	blood:	n/a	n/a
34	CTCF	chr2:100937783-100938083	H1-hESC	embryonic stem cell:	n/a	n/a
35	CTCF	chr2:100938580-100938730	SK-N-SH_RA	brain:	n/a	n/a
36	CTCF	chr2:100937860-100938010	HRPEpiC	eye:	n/a	n/a
37	CTCF	chr2:100937860-100938010	BE2_C	brain:	n/a	n/a
38	CTCF	chr2:100937842-100937973	NHEK	skin:	n/a	n/a
39	CTCF	chr2:100937846-100937942	Lung_OC	lung:	n/a	n/a
40	CTCF	chr2:100937920-100938070	GM12867	blood:	n/a	n/a
41	CTCF	chr2:100937817-100937996	Kidney_OC	kidney:	n/a	n/a
42	CTCF	chr2:100937800-100937950	MCF-7	breast:	n/a	n/a
43	CTCF	chr2:100937780-100937930	NHEK	skin:	n/a	n/a
44	CTCF	chr2:100937800-100937950	GM12866	blood:	n/a	n/a
45	CTCF	chr2:100937840-100937990	HEK293	kidney:	n/a	n/a
46	CTCF	chr2:100937860-100938010	HAc	cerebellar:	n/a	n/a
47	CTCF	chr2:100937860-100938010	HCM	heart:	n/a	n/a
48	CTCF	chr2:100937903-100938008	LNCaP	prostate:	n/a	n/a
49	CTCF	chr2:100937800-100937950	AG04449	skin:	n/a	n/a
50	CTCF	chr2:100937840-100937990	HPAF	blood vessel:	n/a	n/a

(count:733 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:100937944-100937994	ProgFib	skin:	n/a
2	chr2:100937944-100937994	ProgFib	skin:	n/a
3	chr2:100938903-100938953	HMEC	breast:	n/a
4	chr2:100937584-100937634	H1-hESC	embryonic stem cell:	embryo
5	chr2:100939284-100939334	ProgFib	skin:	n/a
6	chr2:100939477-100939527	AG09319	gingival:	n/a
7	chr2:100937505-100937555	HCM	heart:	n/a
8	chr2:100937584-100937634	NT2-D1	testis:	n/a
9	chr2:100937944-100937994	HCT-116	colon:	n/a
10	chr2:100939477-100939527	PANC-1	pancreas:	n/a
11	chr2:100938813-100938863	NH-A	brain:	n/a
12	chr2:100938444-100938494	GM12892	blood:	n/a
13	chr2:100937072-100937122	HL-60	blood:	n/a
14	chr2:100937584-100937634	BE2_C	brain:	n/a
15	chr2:100939045-100939095	HCT-116	colon:	n/a
16	chr2:100937584-100937634	PFSK-1	brain:	n/a
17	chr2:100939477-100939527	GM19239	blood:	n/a
18	chr2:100938799-100938849	PFSK-1	brain:	n/a
19	chr2:100938813-100938863	IMR90	lung:	fetal
20	chr2:100938903-100938953	BJ	skin:	n/a
21	chr2:100939477-100939527	HMEC	breast:	n/a
22	chr2:100937584-100937634	NHDF-neo	bronchial:	n/a
23	chr2:100939045-100939095	GM06990	blood:	n/a
24	chr2:100938813-100938863	GM12891	blood:	n/a
25	chr2:100938799-100938849	LNCaP	prostate:	n/a
26	chr2:100937584-100937634	HCF	heart:	n/a
27	chr2:100939477-100939527	SK-N-SH_RA	brain:	n/a
28	chr2:100938813-100938863	HCT-116	colon:	n/a
29	chr2:100939477-100939527	GM06990	blood:	n/a
30	chr2:100937584-100937634	IMR90	lung:	fetal
31	chr2:100937944-100937994	NT2-D1	testis:	n/a
32	chr2:100937072-100937122	HEEpiC	esophagus:	n/a
33	chr2:100938903-100938953	U87	brain:	n/a
34	chr2:100937796-100937846	PFSK-1	brain:	n/a
35	chr2:100939477-100939527	HRE	kidney:	n/a
36	chr2:100937944-100937994	SK-N-SH_RA	brain:	n/a
37	chr2:100938903-100938953	HCF	heart:	n/a
38	chr2:100937796-100937846	HEK293	kidney:	embryo
39	chr2:100938813-100938863	U87	brain:	n/a
40	chr2:100937505-100937555	ECC-1	luminal epithelium:	n/a
41	chr2:100937505-100937555	HRPEpiC	eye:	n/a
42	chr2:100938813-100938863	Hepatocyte	liver:	n/a
43	chr2:100937796-100937846	HIPEpiC	eye:	n/a
44	chr2:100937796-100937846	MCF10A-Er-Src	breast:	n/a
45	chr2:100938799-100938849	HCM	heart:	n/a
46	chr2:100937505-100937555	GM19239	blood:	n/a
47	chr2:100937505-100937555	CMK	blood:	n/a
48	chr2:100937796-100937846	HL-60	blood:	n/a
49	chr2:100939284-100939334	CMK	blood:	n/a
50	chr2:100937584-100937634	HIPEpiC	eye:	n/a

(count:23 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:100939441..100941644-chr2:100962482..100964041,2	K562	blood:
2	chr2:100933404..100936260-chr2:100953487..100956115,2	K562	blood:
3	chr2:100939645..100941794-chr2:101040138..101041675,2	MCF-7	breast:
4	chr2:100104533..100107300-chr2:100936927..100940750,3	MCF-7	breast:
5	chr2:100937545..100939086-chr2:100943164..100946090,2	K562	blood:
6	chr2:100936794..100939483-chr2:101033248..101035645,2	K562	blood:
7	chr2:100924962..100929454-chr2:100936842..100940898,4	K562	blood:
8	chr2:100908542..100909110-chr2:100937511..100938311,3	MCF-7	breast:
9	chr2:100937085..100941836-chr2:101033510..101036438,4	MCF-7	breast:
10	chr2:100919515..100922139-chr2:100935944..100938623,2	K562	blood:
11	chr2:100940179..100941697-chr2:100950006..100952146,2	MCF-7	breast:
12	chr2:100940171..100942134-chr2:100989571..100992092,2	MCF-7	breast:
13	chr2:100930355..100933148-chr2:100933747..100936603,2	K562	blood:
14	chr2:100877863..100879986-chr2:100936694..100939073,4	MCF-7	breast:
15	chr2:100908492..100909141-chr2:100938432..100939141,2	MCF-7	breast:
16	chr2:100936347..100938622-chr2:101175344..101178245,2	K562	blood:
17	chr2:100937836..100939384-chr2:100985447..100988278,2	K562	blood:
18	chr2:100907864..100908724-chr2:100937511..100938051,2	MCF-7	breast:
19	chr2:100920038..100923906-chr2:100937053..100939083,4	MCF-7	breast:
20	chr2:100629972..100631740-chr2:100936209..100938926,2	MCF-7	breast:
21	chr2:100936567..100938994-chr2:101033479..101035726,2	MCF-7	breast:
22	chr2:100924962..100929082-chr2:100936842..100940898,4	K562	blood:
23	chr2:100940073..100942309-chr2:101029977..101032288,2	K562	blood:

No data

Variant related genes	Relation type
LONRF2	TF binding region
LONRF2	CpG island
ENSG00000170500	chromatin interactions
ENSG00000269383	chromatin interactions
ENSG00000135945	chromatin interactions
ENSG00000115526	chromatin interactions

Extended variants
information (count: 148 )
Associated
traits (count: 55 )

Variant overlapped rSNPs/rCNVs (count:148 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs572012586	chr2:100935957-100935958	Weak transcription Active TSS Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs531246456	chr2:100935965-100935966	Weak transcription Active TSS Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs111852934	chr2:100935985-100935986	Weak transcription Active TSS Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs567867273	chr2:100936100-100936101	Weak transcription Active TSS Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs535930108	chr2:100936104-100936105	Weak transcription Active TSS Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs13391540	chr2:100936124-100936125	Weak transcription Active TSS Flanking Active TSS Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs189130350	chr2:100936162-100936163	Weak transcription Active TSS Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs115565695	chr2:100936165-100936166	Weak transcription Active TSS Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs558419040	chr2:100936168-100936169	Weak transcription Active TSS Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs181543334	chr2:100936175-100936176	Weak transcription Active TSS Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs185808555	chr2:100936202-100936203	Weak transcription Active TSS Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs11123826	chr2:100936276-100936277	Weak transcription Active TSS Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
13	rs574610128	chr2:100936319-100936320	Weak transcription Active TSS Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs73968812	chr2:100936357-100936358	Weak transcription Active TSS Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs75152355	chr2:100936369-100936370	Weak transcription Active TSS Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs528487348	chr2:100936432-100936433	Weak transcription Active TSS Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs553995110	chr2:100936502-100936503	Weak transcription Active TSS Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs565285564	chr2:100936544-100936545	Weak transcription Active TSS Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs143047442	chr2:100936550-100936551	Weak transcription Active TSS Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs11694700	chr2:100936637-100936638	Weak transcription Active TSS Flanking Active TSS Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs551270214	chr2:100936691-100936692	Weak transcription Active TSS Flanking Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs572467643	chr2:100936701-100936702	Weak transcription Active TSS Flanking Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs567740834	chr2:100936716-100936717	Weak transcription Active TSS Flanking Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs148377774	chr2:100936808-100936809	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs368031540	chr2:100936815-100936816	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs115547337	chr2:100936941-100936942	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs371549323	chr2:100936948-100936949	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs34160005	chr2:100936964-100936965	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs538355232	chr2:100936980-100936981	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs551709287	chr2:100937002-100937003	Bivalent Enhancer Enhancers Flanking Active TSS Bivalent/Poised TSS Active TSS Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs568856819	chr2:100937013-100937014	Bivalent Enhancer Enhancers Flanking Active TSS Bivalent/Poised TSS Active TSS Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs537734542	chr2:100937062-100937063	Bivalent Enhancer Enhancers Flanking Active TSS Bivalent/Poised TSS Active TSS Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs536259779	chr2:100937085-100937086	Bivalent Enhancer Enhancers Flanking Active TSS Bivalent/Poised TSS Active TSS Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs182720420	chr2:100937094-100937095	Bivalent Enhancer Enhancers Flanking Active TSS Bivalent/Poised TSS Active TSS Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs574545267	chr2:100937131-100937132	Bivalent Enhancer Enhancers Flanking Active TSS Bivalent/Poised TSS Active TSS Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs114766847	chr2:100937182-100937183	Bivalent Enhancer Enhancers Flanking Active TSS Bivalent/Poised TSS Active TSS Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs141601340	chr2:100937185-100937186	Bivalent Enhancer Enhancers Flanking Active TSS Bivalent/Poised TSS Active TSS Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs573328924	chr2:100937215-100937216	Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs371904246	chr2:100937280-100937281	Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs145889824	chr2:100937299-100937300	Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs575626120	chr2:100937311-100937312	Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs138443005	chr2:100937327-100937328	Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs554900714	chr2:100937332-100937333	Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs7582424	chr2:100937407-100937408	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Active TSS Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs374381953	chr2:100937435-100937436	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Active TSS Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs546749275	chr2:100937444-100937445	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Active TSS Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs560316200	chr2:100937451-100937452	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Active TSS Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs532049216	chr2:100937459-100937460	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Active TSS Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs576356379	chr2:100937465-100937466	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Active TSS Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs540418345	chr2:100937467-100937468	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Active TSS Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:55)

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
T-cell prolymphocytic leukemia	17713554	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Melanoma	20877625	CNVD
Breast cancer	22522925	CNVD
Schizophrenia	23813976	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:326 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:100901000-100937000	Weak transcription	Fetal Brain Male	brain
2	chr2:100918200-100937600	Weak transcription	Aorta	Aorta
3	chr2:100924200-100936800	Weak transcription	Brain Cingulate Gyrus	brain
4	chr2:100924600-100936000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
5	chr2:100929800-100937000	Weak transcription	Pancreas	Pancrea
6	chr2:100930800-100937000	Weak transcription	Brain Hippocampus Middle	brain
7	chr2:100935000-100936000	Weak transcription	Brain Angular Gyrus	brain
8	chr2:100935200-100936000	Weak transcription	Brain Anterior Caudate	brain
9	chr2:100935200-100936000	Weak transcription	A549	lung
10	chr2:100935200-100936200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
11	chr2:100935200-100937000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
12	chr2:100935200-100937000	Weak transcription	Ovary	ovary
13	chr2:100935200-100937000	Weak transcription	K562	blood
14	chr2:100935600-100936600	Weak transcription	Cortex derived primary cultured neurospheres	brain
15	chr2:100935800-100936400	Flanking Active TSS	Pancreatic Islets	Pancreatic Islet
16	chr2:100935800-100937000	Enhancers	Skeletal Muscle Male	skeletal muscle
17	chr2:100935800-100937400	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
18	chr2:100935800-100939400	Active TSS	Brain Inferior Temporal Lobe	brain
19	chr2:100936000-100936200	Flanking Active TSS	Brain Angular Gyrus	brain
20	chr2:100936000-100936800	Active TSS	Brain Anterior Caudate	brain
21	chr2:100936000-100938800	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
22	chr2:100936000-100939400	Active TSS	A549	lung
23	chr2:100936200-100936400	Enhancers	Duodenum Smooth Muscle	Duodenum
24	chr2:100936200-100936400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
25	chr2:100936200-100936400	Enhancers	Fetal Brain Female	brain
26	chr2:100936200-100937000	Active TSS	Brain Angular Gyrus	brain
27	chr2:100936400-100936600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
28	chr2:100936400-100936600	Active TSS	Pancreatic Islets	Pancreatic Islet
29	chr2:100936400-100937800	Flanking Active TSS	Fetal Brain Female	brain
30	chr2:100936600-100936800	Flanking Active TSS	Pancreatic Islets	Pancreatic Islet
31	chr2:100936600-100937000	Active TSS	Cortex derived primary cultured neurospheres	brain
32	chr2:100936600-100937400	Active TSS	Fetal Adrenal Gland	Adrenal Gland
33	chr2:100936800-100937000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
34	chr2:100936800-100937000	Enhancers	Brain Germinal Matrix	brain
35	chr2:100936800-100937200	Flanking Active TSS	Brain Anterior Caudate	brain
36	chr2:100936800-100937600	Flanking Active TSS	Brain Cingulate Gyrus	brain
37	chr2:100936800-100939400	Active TSS	Pancreatic Islets	Pancreatic Islet
38	chr2:100937000-100937200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
39	chr2:100937000-100937200	Flanking Active TSS	Brain Hippocampus Middle	brain
40	chr2:100937000-100937200	Active TSS	Brain Substantia Nigra	brain
41	chr2:100937000-100937200	Enhancers	Right Atrium	heart
42	chr2:100937000-100937200	Active TSS	Skeletal Muscle Female	skeletal muscle
43	chr2:100937000-100937400	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
44	chr2:100937000-100937400	Flanking Active TSS	Brain Angular Gyrus	brain
45	chr2:100937000-100937400	Active TSS	Duodenum Smooth Muscle	Duodenum
46	chr2:100937000-100937400	Active TSS	Pancreas	Pancrea
47	chr2:100937000-100937400	Active TSS	Stomach Mucosa	stomach
48	chr2:100937000-100937600	Flanking Active TSS	Colon Smooth Muscle	Colon
49	chr2:100937000-100937600	Active TSS	Fetal Brain Male	brain
50	chr2:100937000-100937600	Flanking Active TSS	K562	blood

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