Variant report

Variant	esv1796304
Chromosome Location	chr2:38766721-38790750
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:828)
CpG islands
(count:61)
Chromatin interactive
region (count:55)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:828 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:38782471-38782599	K562	blood:	n/a	n/a
2	ARID3A	chr2:38782437-38782683	HepG2	liver:	n/a	n/a
3	ARID3A	chr2:38768476-38769081	HepG2	liver:	n/a	n/a
4	ARID3A	chr2:38769998-38770403	K562	blood:	n/a	n/a
5	ARID3A	chr2:38767539-38767594	HepG2	liver:	n/a	n/a
6	ARID3A	chr2:38769688-38770404	HepG2	liver:	n/a	n/a
7	ARID3A	chr2:38779208-38779861	K562	blood:	n/a	n/a
8	ATF1	chr2:38769983-38770420	K562	blood:	n/a	n/a
9	ATF1	chr2:38783262-38783383	K562	blood:	n/a	n/a
10	ATF1	chr2:38779453-38779757	K562	blood:	n/a	n/a
11	ATF3	chr2:38779416-38779784	K562	blood:	n/a	n/a
12	BACH1	chr2:38767789-38767821	K562	blood:	n/a	n/a
13	BACH1	chr2:38779659-38779858	K562	blood:	n/a	n/a
14	BACH1	chr2:38769982-38770286	K562	blood:	n/a	n/a
15	BACH1	chr2:38782673-38782688	K562	blood:	n/a	n/a
16	BACH1	chr2:38769939-38770322	H1-hESC	embryonic stem cell:	n/a	n/a
17	BCL3	chr2:38783614-38783969	GM12878	blood:	n/a	n/a
18	BCL3	chr2:38769500-38770446	A549	lung:	n/a	n/a
19	BHLHE40	chr2:38770032-38770409	HepG2	liver:	n/a	n/a
20	BHLHE40	chr2:38779467-38779809	K562	blood:	n/a	n/a
21	BHLHE40	chr2:38782526-38782598	K562	blood:	n/a	n/a
22	BHLHE40	chr2:38770019-38770430	K562	blood:	n/a	n/a
23	CBX3	chr2:38779315-38779856	K562	blood:	n/a	n/a
24	CBX3	chr2:38769990-38770442	K562	blood:	n/a	n/a
25	CBX3	chr2:38769868-38770522	HCT-116	colon:	n/a	n/a
26	CBX3	chr2:38769414-38770581	HCT-116	colon:	n/a	n/a
27	CCNT2	chr2:38769921-38770349	K562	blood:	n/a	n/a
28	CCNT2	chr2:38776054-38776376	K562	blood:	n/a	n/a
29	CCNT2	chr2:38779134-38780012	K562	blood:	n/a	n/a
30	CCNT2	chr2:38784417-38784598	K562	blood:	n/a	n/a
31	CCNT2	chr2:38782227-38782796	K562	blood:	n/a	n/a
32	CEBPB	chr2:38770117-38770428	A549	lung:	n/a	n/a
33	CEBPB	chr2:38768870-38769267	ECC-1	luminal epithelium:	n/a	chr2:38769091-38769104
34	CEBPB	chr2:38770023-38770431	HepG2	liver:	n/a	n/a
35	CEBPB	chr2:38769969-38770390	HepG2	liver:	n/a	n/a
36	CEBPB	chr2:38769879-38770725	HCT-116	colon:	n/a	n/a
37	CEBPB	chr2:38769914-38770612	HCT-116	colon:	n/a	n/a
38	CEBPB	chr2:38770033-38770428	IMR90	lung:	n/a	n/a
39	CEBPB	chr2:38770051-38770432	HepG2	liver:	n/a	n/a
40	CEBPB	chr2:38769939-38770549	A549	lung:	n/a	n/a
41	CEBPB	chr2:38769969-38770550	K562	blood:	n/a	n/a
42	CEBPB	chr2:38779200-38779746	K562	blood:	n/a	n/a
43	CEBPB	chr2:38778436-38778633	HepG2	liver:	n/a	chr2:38778502-38778513
44	CEBPB	chr2:38769997-38770434	K562	blood:	n/a	n/a
45	CEBPB	chr2:38770035-38770422	Hela-S3	cervix:	n/a	n/a
46	CEBPB	chr2:38778371-38778656	K562	blood:	n/a	chr2:38778502-38778513
47	CEBPB	chr2:38770108-38770663	H1-hESC	embryonic stem cell:	n/a	n/a
48	CEBPB	chr2:38770061-38770439	K562	blood:	n/a	n/a
49	CEBPB	chr2:38770104-38770385	HepG2	liver:	n/a	n/a
50	CEBPD	chr2:38779253-38779886	K562	blood:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:38769204-38769254	SKMC	muscle:	n/a
2	chr2:38769204-38769254	Jurkat	blood:	n/a
3	chr2:38769204-38769254	HRCEpiC	kidney:	n/a
4	chr2:38769204-38769254	HEK293	kidney:	embryo
5	chr2:38769204-38769254	HNPCEpiC	eye:	n/a
6	chr2:38769204-38769254	SAEC	small airway:	n/a
7	chr2:38769204-38769254	HPAEpiC	pulmonary alveolar:	n/a
8	chr2:38769204-38769254	AoSMC	blood vessel:	n/a
9	chr2:38769204-38769254	Hepatocyte	liver:	n/a
10	chr2:38769204-38769254	SK-N-MC	brain:	n/a
11	chr2:38769204-38769254	HUVEC	blood vessel:	n/a
12	chr2:38769204-38769254	IMR90	lung:	fetal
13	chr2:38769204-38769254	HEEpiC	esophagus:	n/a
14	chr2:38769204-38769254	MCF10A-Er-Src	breast:	n/a
15	chr2:38769204-38769254	AG04449	skin:	fetal
16	chr2:38769204-38769254	NHBE	bronchial:	n/a
17	chr2:38769204-38769254	NHDF-neo	bronchial:	n/a
18	chr2:38769204-38769254	NB4	blood:	n/a
19	chr2:38769204-38769254	HRPEpiC	eye:	n/a
20	chr2:38769204-38769254	NT2-D1	testis:	n/a
21	chr2:38769204-38769254	SK-N-SH	brain:	n/a
22	chr2:38769204-38769254	AG09319	gingival:	n/a
23	chr2:38769204-38769254	ProgFib	skin:	n/a
24	chr2:38769204-38769254	GM12892	blood:	n/a
25	chr2:38769204-38769254	HAEpiC	amniotic membrane:	n/a
26	chr2:38769204-38769254	NH-A	brain:	n/a
27	chr2:38769204-38769254	HMEC	breast:	n/a
28	chr2:38769204-38769254	PFSK-1	brain:	n/a
29	chr2:38769204-38769254	CMK	blood:	n/a
30	chr2:38769204-38769254	HIPEpiC	eye:	n/a
31	chr2:38769204-38769254	GM12891	blood:	n/a
32	chr2:38769204-38769254	PANC-1	pancreas:	n/a
33	chr2:38769204-38769254	AG09309	skin:	n/a
34	chr2:38769204-38769254	Hela-S3	cervix:	n/a
35	chr2:38769204-38769254	RPTEC	kidney:	n/a
36	chr2:38769204-38769254	BE2_C	brain:	n/a
37	chr2:38769204-38769254	H1-hESC	embryonic stem cell:	embryo
38	chr2:38769204-38769254	ovcar-3	ovarian:	n/a
39	chr2:38769204-38769254	A549	lung:	n/a
40	chr2:38769204-38769254	PrEC	prostate:	n/a
41	chr2:38769204-38769254	LNCaP	prostate:	n/a
42	chr2:38769204-38769254	HCM	heart:	n/a
43	chr2:38769204-38769254	GM12878	blood:	n/a
44	chr2:38769204-38769254	GM19239	blood:	n/a
45	chr2:38769204-38769254	ECC-1	luminal epithelium:	n/a
46	chr2:38769204-38769254	K562	blood:	n/a
47	chr2:38769204-38769254	U87	brain:	n/a
48	chr2:38769204-38769254	HCPEpiC	choroid plexus:	n/a
49	chr2:38769204-38769254	Caco-2	colon:	n/a
50	chr2:38769204-38769254	HRE	kidney:	n/a

(count:55 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr2:38783037..38784703-chr2:38789757..38791472,2	K562	blood:
2	chr2:38788213..38790440-chr2:38791482..38793499,2	MCF-7	breast:
3	chr2:38781921..38784416-chr2:38785346..38789078,4	K562	blood:
4	chr2:38773369..38778839-chr2:38780028..38785171,8	K562	blood:
5	chr2:38778255..38779937-chr2:38819083..38821616,2	K562	blood:
6	chr2:38766439..38768320-chr2:38948180..38949983,2	K562	blood:
7	chr2:38761874..38764220-chr2:38767689..38769957,3	K562	blood:
8	chr2:38780198..38783785-chr2:38971693..38974497,3	K562	blood:
9	chr2:38768041..38770034-chr2:38779562..38781817,2	K562	blood:
10	chr2:38781921..38784416-chr2:38785346..38789078,4	K562	blood:
11	chr2:38771358..38773327-chr2:38795004..38797388,2	K562	blood:
12	chr2:38769946..38771644-chr2:38978190..38979713,2	MCF-7	breast:
13	chr2:38778308..38780052-chr2:38967008..38969234,2	K562	blood:
14	chr2:38741728..38744582-chr2:38773775..38776381,2	K562	blood:
15	chr2:38767365..38769438-chr2:38773461..38775183,2	MCF-7	breast:
16	chr2:38780413..38785333-chr2:38976910..38979938,6	K562	blood:
17	chr2:38773369..38778839-chr2:38780028..38785171,8	K562	blood:
18	chr2:38762206..38765447-chr2:38765522..38767637,3	K562	blood:
19	chr2:38778308..38782276-chr2:38966801..38969709,4	K562	blood:
20	chr2:38776554..38778945-chr2:38971889..38973441,2	K562	blood:
21	chr2:38777679..38779633-chr2:38893883..38895640,2	K562	blood:
22	chr2:38783818..38787523-chr2:38967718..38971056,4	K562	blood:
23	chr2:38788831..38791185-chr2:38805225..38808104,2	K562	blood:
24	chr2:38788017..38790362-chr2:38797831..38799646,2	K562	blood:
25	chr2:38772538..38776626-chr2:38827465..38831623,3	K562	blood:
26	chr2:38771801..38777092-chr2:38966712..38971904,5	K562	blood:
27	chr2:38767365..38769438-chr2:38773461..38775183,2	MCF-7	breast:
28	chr2:38786392..38790076-chr2:38975715..38979796,3	MCF-7	breast:
29	chr2:38779577..38781346-chr2:38785397..38787246,2	K562	blood:
30	chr2:38789671..38792493-chr2:38794014..38797710,4	K562	blood:
31	chr2:38776394..38779089-chr2:38793854..38796056,2	MCF-7	breast:
32	chr2:38751112..38753312-chr2:38768692..38771301,2	K562	blood:
33	chr2:38777342..38780101-chr2:38971109..38972812,2	K562	blood:
34	chr2:38766012..38769150-chr2:38977122..38980582,4	K562	blood:
35	chr2:38765872..38769105-chr2:38828205..38830691,3	MCF-7	breast:
36	chr2:38782096..38782773-chr2:39005282..39006019,3	MCF-7	breast:
37	chr2:38756770..38758760-chr2:38767027..38769567,2	K562	blood:
38	chr2:38782046..38785023-chr2:38977532..38979938,4	K562	blood:
39	chr2:38767755..38769303-chr2:38769457..38771424,2	K562	blood:
40	chr2:38779577..38781346-chr2:38785397..38787246,2	K562	blood:
41	chr2:38751052..38753238-chr2:38767165..38769647,2	MCF-7	breast:
42	chr2:38783037..38784703-chr2:38789757..38791472,2	K562	blood:
43	chr2:38770232..38774244-chr2:38976034..38979615,5	K562	blood:
44	chr2:38767755..38769303-chr2:38769457..38771424,2	K562	blood:
45	chr2:38786011..38787740-chr2:38976954..38979344,3	K562	blood:
46	chr2:38742072..38744914-chr2:38766653..38769930,3	K562	blood:
47	chr2:38601876..38603908-chr2:38779549..38781640,2	K562	blood:
48	chr2:38782788..38784491-chr2:38951489..38953190,2	K562	blood:
49	chr2:38768041..38770034-chr2:38779562..38781817,2	K562	blood:
50	chr2:38776916..38778592-chr2:38969344..38970967,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-HNRPLL-4	chr2:38787215-38789656	NONHSAT070189
2	lnc-HNRPLL-1	chr2:38767123-38768717	XLOC_002054
3	lnc-HNRPLL-1	chr2:38768888-38769283	XLOC_002054

No data

Variant related genes	Relation type
ENSG00000271443	TF binding region
ENSG00000271443	CpG island
ENSG00000231367	chromatin interactions
ENSG00000119787	chromatin interactions
ENSG00000152147	chromatin interactions
ENSG00000115875	chromatin interactions
ENSG00000235586	chromatin interactions
ENSG00000271443	chromatin interactions
ENSG00000143889	chromatin interactions

Extended variants
information (count: 1045 )
Associated
traits (count: 60 )

Variant overlapped rSNPs/rCNVs (count:1045 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs566500913	chr2:38766721-38766722	Weak transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
2	rs534013031	chr2:38766725-38766726	Weak transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
3	rs558541305	chr2:38766858-38766859	Weak transcription Enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
4	rs61141629	chr2:38766918-38766919	Weak transcription Enhancers	Chromatin interactive region	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs538627868	chr2:38766920-38766921	Weak transcription Enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
6	rs556984781	chr2:38766929-38766930	Weak transcription Enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
7	rs549333607	chr2:38766941-38766942	Weak transcription Enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
8	rs78434935	chr2:38766942-38766943	Weak transcription Enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
9	rs558465341	chr2:38766958-38766959	Weak transcription Enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
10	rs188927795	chr2:38767054-38767055	Weak transcription Enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
11	rs181291786	chr2:38767066-38767067	Weak transcription Enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
12	rs377580516	chr2:38767094-38767095	Weak transcription Enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
13	rs555064689	chr2:38767133-38767134	Weak transcription Enhancers	TF binding region Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a
14	rs17603675	chr2:38767134-38767135	Weak transcription Enhancers	TF binding region Chromatin interactive region lncRNA	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs7578342	chr2:38767148-38767149	Weak transcription Enhancers	TF binding region Chromatin interactive region lncRNA	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs565556225	chr2:38767216-38767217	Weak transcription Enhancers	TF binding region Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a
17	rs77203341	chr2:38767375-38767376	Weak transcription Enhancers	TF binding region Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a
18	rs183921959	chr2:38767383-38767384	Weak transcription Enhancers	TF binding region Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a
19	rs546310751	chr2:38767440-38767441	Weak transcription Enhancers	TF binding region Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a
20	rs562429009	chr2:38767464-38767465	Weak transcription Enhancers	TF binding region Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a
21	rs17421378	chr2:38767505-38767506	Weak transcription Enhancers	TF binding region Chromatin interactive region lncRNA	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs13388732	chr2:38767521-38767522	Weak transcription Enhancers	TF binding region Chromatin interactive region lncRNA	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs141751382	chr2:38767522-38767523	Weak transcription Enhancers	TF binding region Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a
24	rs74895229	chr2:38767554-38767555	Weak transcription Enhancers	TF binding region Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a
25	rs7605576	chr2:38767586-38767587	Weak transcription Enhancers	TF binding region Chromatin interactive region lncRNA	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs189721064	chr2:38767658-38767659	Weak transcription Enhancers	TF binding region Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a
27	rs367863281	chr2:38767715-38767716	Weak transcription Enhancers	TF binding region Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a
28	rs537790236	chr2:38767727-38767728	Weak transcription Enhancers	TF binding region Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a
29	rs78243567	chr2:38767809-38767810	Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a
30	rs568881175	chr2:38767824-38767825	Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a
31	rs536663254	chr2:38767835-38767836	Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a
32	rs150559152	chr2:38767855-38767856	Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a
33	rs180964512	chr2:38767928-38767929	Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a
34	rs76173670	chr2:38767960-38767961	Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a
35	rs185907409	chr2:38767972-38767973	Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a
36	rs368302755	chr2:38767985-38767986	Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a
37	rs74859787	chr2:38767986-38767987	Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a
38	rs578012740	chr2:38768003-38768004	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a
39	rs544873279	chr2:38768012-38768013	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a
40	rs78353523	chr2:38768019-38768020	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a
41	rs192001034	chr2:38768026-38768027	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a
42	rs111939868	chr2:38768063-38768064	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a
43	rs541847336	chr2:38768080-38768081	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a
44	rs372018250	chr2:38768180-38768181	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a
45	rs527429357	chr2:38768252-38768253	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a
46	rs551945440	chr2:38768270-38768271	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a
47	rs148420611	chr2:38768305-38768306	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a
48	rs78254185	chr2:38768358-38768359	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a
49	rs79748883	chr2:38768388-38768389	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a
50	rs6732743	chr2:38768464-38768465	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region lncRNA	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance

Variant related diseases (count:60)

Disease	PMID	Source
Breast cancer	17393978	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Breast cancer	17603634	CNVD
Medulloblastoma	21979893	CNVD
Lynch syndrome	18415027	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
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
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Ependymoma	16718352	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
lymphocytic leukemia	21291569	CNVD
Prostate cancer	18632612	CNVD
Bladder cancer	21909424	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Autism	22495311	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Follicular lymphoma	20505157	CNVD
Autism	17483303	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Medulloblastoma	20607354	CNVD
Leukemia	18628472	CNVD
Autism	19521722	CNVD
Autism	18522746	CNVD
Non-small cell lung cancer	18927303	CNVD
Breast cancer	21785460	CNVD
Lung cancer	18438408	CNVD
Prostate cancer	21965145	CNVD
Breast cancer	16397240	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	21508638	CNVD
Neurodevelopmental disorder	22521361	CNVD
Neurocytoma	17123091	CNVD
small cell lung cancer	20016488	CNVD
Melanoma	18172304	CNVD
Cancer	16751803	CNVD
Breast cancer	21364760	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Colorectal cancer	16272173	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:623 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:38763400-38768000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr2:38763600-38767200	Weak transcription	Esophagus	oesophagus
3	chr2:38763600-38767400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
4	chr2:38763600-38767600	Weak transcription	Rectal Mucosa Donor 29	rectum
5	chr2:38763600-38767800	Weak transcription	Stomach Mucosa	stomach
6	chr2:38763600-38768200	Weak transcription	H9 Cell Line	embryonic stem cell
7	chr2:38763600-38768200	Weak transcription	HUES48 Cell Line	embryonic stem cell
8	chr2:38763600-38768400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
9	chr2:38763600-38768800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
10	chr2:38763600-38769000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
11	chr2:38763600-38770200	Weak transcription	HSMMtube	muscle
12	chr2:38763600-38771000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
13	chr2:38763600-38809600	Weak transcription	Placenta Amnion	Placenta Amnion
14	chr2:38763800-38767200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
15	chr2:38763800-38767400	Weak transcription	Fetal Brain Female	brain
16	chr2:38763800-38767600	Weak transcription	Cortex derived primary cultured neurospheres	brain
17	chr2:38763800-38767600	Weak transcription	Colon Smooth Muscle	Colon
18	chr2:38763800-38767600	Weak transcription	Fetal Brain Male	brain
19	chr2:38763800-38767600	Weak transcription	Fetal Intestine Large	intestine
20	chr2:38763800-38767600	Weak transcription	Fetal Intestine Small	intestine
21	chr2:38763800-38767600	Weak transcription	Rectal Smooth Muscle	rectum
22	chr2:38763800-38767800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
23	chr2:38763800-38767800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
24	chr2:38763800-38767800	Weak transcription	Duodenum Smooth Muscle	Duodenum
25	chr2:38763800-38768400	Weak transcription	HUES64 Cell Line	embryonic stem cell
26	chr2:38763800-38768600	Weak transcription	Brain Anterior Caudate	brain
27	chr2:38763800-38769000	Weak transcription	Primary T helper cells PMA-I stimulated	--
28	chr2:38763800-38769400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
29	chr2:38763800-38769800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
30	chr2:38763800-38778800	Weak transcription	Skeletal Muscle Female	skeletal muscle
31	chr2:38764000-38767400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
32	chr2:38764200-38767400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
33	chr2:38764200-38768400	Weak transcription	Liver	Liver
34	chr2:38764200-38769600	Weak transcription	A549	lung
35	chr2:38765600-38768200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
36	chr2:38765600-38768400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
37	chr2:38765800-38768000	Enhancers	HepG2	liver
38	chr2:38766400-38766800	Enhancers	H1 Cell Line	embryonic stem cell
39	chr2:38766600-38767600	Weak transcription	HUES6 Cell Line	embryonic stem cell
40	chr2:38766600-38768200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
41	chr2:38766600-38768200	Weak transcription	Duodenum Mucosa	Duodenum
42	chr2:38766800-38768200	Weak transcription	H1 Cell Line	embryonic stem cell
43	chr2:38767200-38769400	Enhancers	Breast Myoepithelial Primary Cells	Breast
44	chr2:38767400-38768400	Enhancers	Fetal Brain Female	brain
45	chr2:38767400-38768400	Enhancers	Sigmoid Colon	Sigmoid Colon
46	chr2:38767400-38768600	Enhancers	Rectal Mucosa Donor 31	rectum
47	chr2:38767400-38768800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
48	chr2:38767400-38770000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
49	chr2:38767400-38773400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
50	chr2:38767600-38768400	Enhancers	Rectal Mucosa Donor 29	rectum

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