Variant report

Variant	esv1800732
Chromosome Location	chr2:38951608-38973837
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:995)
CpG islands
(count:123)
Chromatin interactive
region (count:75)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:12)

(count:995 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:38968085-38968382	K562	blood:	n/a	n/a
2	ARID3A	chr2:38969026-38969567	HepG2	liver:	n/a	n/a
3	ARID3A	chr2:38953213-38953354	K562	blood:	n/a	n/a
4	ARID3A	chr2:38968049-38968417	HepG2	liver:	n/a	n/a
5	ARID3A	chr2:38957567-38957767	HepG2	liver:	n/a	n/a
6	ARID3A	chr2:38960583-38960998	HepG2	liver:	n/a	n/a
7	ARID3A	chr2:38958825-38959337	HepG2	liver:	n/a	n/a
8	ATF2	chr2:38970329-38971016	H1-hESC	embryonic stem cell:	n/a	n/a
9	ATF2	chr2:38971052-38971500	H1-hESC	embryonic stem cell:	n/a	n/a
10	ATF2	chr2:38969791-38970170	H1-hESC	embryonic stem cell:	n/a	n/a
11	ATF2	chr2:38953102-38953411	GM12878	blood:	n/a	n/a
12	ATF3	chr2:38966713-38966989	K562	blood:	n/a	n/a
13	BCL3	chr2:38970097-38971823	K562	blood:	n/a	n/a
14	BCL3	chr2:38967993-38968638	A549	lung:	n/a	n/a
15	BCL3	chr2:38970620-38971557	A549	lung:	n/a	n/a
16	BCL3	chr2:38969826-38970596	A549	lung:	n/a	n/a
17	BCL3	chr2:38970314-38970670	K562	blood:	n/a	n/a
18	BCL3	chr2:38968167-38968631	A549	lung:	n/a	n/a
19	BCLAF1	chr2:38969864-38970331	GM12878	blood:	n/a	n/a
20	BCLAF1	chr2:38969857-38970244	GM12878	blood:	n/a	n/a
21	BCLAF1	chr2:38969877-38971863	K562	blood:	n/a	n/a
22	BCLAF1	chr2:38970745-38971762	K562	blood:	n/a	n/a
23	BHLHE40	chr2:38957732-38957923	HepG2	liver:	n/a	n/a
24	BHLHE40	chr2:38970388-38970677	K562	blood:	n/a	n/a
25	BRCA1	chr2:38968158-38968358	Hela-S3	cervix:	n/a	n/a
26	CBX3	chr2:38966528-38967101	K562	blood:	n/a	n/a
27	CBX3	chr2:38966627-38967081	K562	blood:	n/a	n/a
28	CBX3	chr2:38967982-38968397	K562	blood:	n/a	n/a
29	CCNT2	chr2:38970132-38970513	K562	blood:	n/a	n/a
30	CEBPB	chr2:38971156-38971289	K562	blood:	n/a	n/a
31	CEBPB	chr2:38970083-38970592	Hela-S3	cervix:	n/a	chr2:38970438-38970449 chr2:38970222-38970233
32	CEBPB	chr2:38970072-38970600	A549	lung:	n/a	chr2:38970438-38970449 chr2:38970222-38970233
33	CEBPB	chr2:38970063-38970499	K562	blood:	n/a	chr2:38970438-38970449 chr2:38970222-38970233
34	CEBPB	chr2:38960788-38961059	HepG2	liver:	n/a	n/a
35	CEBPB	chr2:38960835-38961036	HepG2	liver:	n/a	n/a
36	CEBPB	chr2:38970114-38970254	HepG2	liver:	n/a	chr2:38970222-38970233
37	CEBPB	chr2:38970095-38970305	H1-hESC	embryonic stem cell:	n/a	chr2:38970222-38970233
38	CEBPB	chr2:38964278-38964893	ECC-1	luminal epithelium:	n/a	n/a
39	CEBPB	chr2:38970089-38970536	IMR90	lung:	n/a	chr2:38970438-38970449 chr2:38970222-38970233
40	CEBPB	chr2:38964265-38964887	ECC-1	luminal epithelium:	n/a	n/a
41	CEBPB	chr2:38964006-38964062	K562	blood:	n/a	n/a
42	CEBPB	chr2:38970069-38970331	HepG2	liver:	n/a	chr2:38970222-38970233
43	CEBPB	chr2:38969926-38970577	K562	blood:	n/a	chr2:38970438-38970449 chr2:38970222-38970233
44	CHD1	chr2:38970531-38970922	H1-hESC	embryonic stem cell:	n/a	n/a
45	CHD2	chr2:38958888-38959088	HepG2	liver:	n/a	n/a
46	CHD2	chr2:38970934-38971927	H1-hESC	embryonic stem cell:	n/a	n/a
47	CHD2	chr2:38973426-38973591	H1-hESC	embryonic stem cell:	n/a	n/a
48	CTCF	chr2:38968190-38968264	LNCaP	prostate:	n/a	chr2:38968192-38968210 chr2:38968193-38968209
49	CTCF	chr2:38968032-38968356	Spleen_OC	spleen:	n/a	chr2:38968192-38968210 chr2:38968187-38968208 chr2:38968193-38968209
50	CTCF	chr2:38953160-38953310	BE2_C	brain:	n/a	n/a

(count:123 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:38970936-38970986	HNPCEpiC	eye:	n/a
2	chr2:38970936-38970986	HNPCEpiC	eye:	n/a
3	chr2:38961590-38961640	IMR90	lung:	fetal
4	chr2:38961590-38961640	K562	blood:	n/a
5	chr2:38961590-38961640	AG04449	skin:	fetal
6	chr2:38961590-38961640	BJ	skin:	n/a
7	chr2:38961590-38961640	ProgFib	skin:	n/a
8	chr2:38961590-38961640	GM12878	blood:	n/a
9	chr2:38961590-38961640	GM12892	blood:	n/a
10	chr2:38970936-38970986	NT2-D1	testis:	n/a
11	chr2:38970936-38970986	GM12892	blood:	n/a
12	chr2:38970936-38970986	AG04450	lung:	fetal
13	chr2:38970936-38970986	NB4	blood:	n/a
14	chr2:38961590-38961640	PrEC	prostate:	n/a
15	chr2:38970936-38970986	HCPEpiC	choroid plexus:	n/a
16	chr2:38970936-38970986	PANC-1	pancreas:	n/a
17	chr2:38970936-38970986	HEEpiC	esophagus:	n/a
18	chr2:38970936-38970986	SK-N-MC	brain:	n/a
19	chr2:38961590-38961640	ECC-1	luminal epithelium:	n/a
20	chr2:38961590-38961640	NHBE	bronchial:	n/a
21	chr2:38970936-38970986	HCM	heart:	n/a
22	chr2:38961590-38961640	MCF10A-Er-Src	breast:	n/a
23	chr2:38961590-38961640	CMK	blood:	n/a
24	chr2:38961590-38961640	HCPEpiC	choroid plexus:	n/a
25	chr2:38970936-38970986	HepG2	liver:	n/a
26	chr2:38970936-38970986	Hepatocyte	liver:	n/a
27	chr2:38970936-38970986	ECC-1	luminal epithelium:	n/a
28	chr2:38961590-38961640	NT2-D1	testis:	n/a
29	chr2:38970936-38970986	A549	lung:	n/a
30	chr2:38970936-38970986	H1-hESC	embryonic stem cell:	embryo
31	chr2:38970936-38970986	HL-60	blood:	n/a
32	chr2:38961590-38961640	HIPEpiC	eye:	n/a
33	chr2:38961590-38961640	AG10803	skin:	n/a
34	chr2:38970936-38970986	IMR90	lung:	fetal
35	chr2:38961590-38961640	RPTEC	kidney:	n/a
36	chr2:38961590-38961640	HCM	heart:	n/a
37	chr2:38970936-38970986	BJ	skin:	n/a
38	chr2:38961590-38961640	SK-N-SH	brain:	n/a
39	chr2:38961590-38961640	Hepatocyte	liver:	n/a
40	chr2:38961590-38961640	AoSMC	blood vessel:	n/a
41	chr2:38970936-38970986	HAEpiC	amniotic membrane:	n/a
42	chr2:38961590-38961640	HRCEpiC	kidney:	n/a
43	chr2:38961590-38961640	NB4	blood:	n/a
44	chr2:38961590-38961640	NH-A	brain:	n/a
45	chr2:38970936-38970986	PFSK-1	brain:	n/a
46	chr2:38970936-38970986	U87	brain:	n/a
47	chr2:38970936-38970986	SK-N-SH_RA	brain:	n/a
48	chr2:38970936-38970986	MCF-7	breast:	n/a
49	chr2:38970936-38970986	HEK293	kidney:	embryo
50	chr2:38970936-38970986	GM06990	blood:	n/a

(count:75 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr2:38969744..38972668-chr2:39079063..39081917,2	K562	blood:
2	chr2:38821957..38830238-chr2:38965333..38974515,17	K562	blood:
3	chr2:38971477..38974181-chr2:39070212..39071979,2	K562	blood:
4	chr2:38797642..38800500-chr2:38970154..38972893,3	K562	blood:
5	chr2:38806248..38808565-chr2:38954475..38956582,2	K562	blood:
6	chr2:38973415..38975366-chr2:39100938..39103537,2	K562	blood:
7	chr2:38973025..38976072-chr2:38989424..38992491,3	MCF-7	breast:
8	chr2:38890926..38894484-chr2:38966717..38969696,3	K562	blood:
9	chr2:38824026..38825901-chr2:38962946..38965190,2	K562	blood:
10	chr2:38825865..38831347-chr2:38967441..38973263,7	MCF-7	breast:
11	chr2:38948167..38950183-chr2:38951156..38954719,3	MCF-7	breast:
12	chr2:38951822..38954678-chr2:38974984..38978674,3	MCF-7	breast:
13	chr2:38970433..38973202-chr2:39101561..39103426,2	K562	blood:
14	chr2:38777342..38780101-chr2:38971109..38972812,2	K562	blood:
15	chr2:38782788..38784491-chr2:38951489..38953190,2	K562	blood:
16	chr2:38966114..38968421-chr2:39005419..39007550,2	MCF-7	breast:
17	chr2:38842870..38845739-chr2:38968254..38970613,2	K562	blood:
18	chr2:38957599..38960532-chr2:38963906..38966818,3	MCF-7	breast:
19	chr2:38761989..38764024-chr2:38963798..38966475,2	K562	blood:
20	chr2:38749544..38751613-chr2:38963489..38965052,2	K562	blood:
21	chr2:38892250..38893779-chr2:38950404..38953319,2	MCF-7	breast:
22	chr2:38952964..38955147-chr2:38962662..38964178,2	K562	blood:
23	chr2:38763105..38763665-chr2:38968175..38968815,2	MCF-7	breast:
24	chr2:38800582..38805538-chr2:38967531..38972325,7	K562	blood:
25	chr2:38812717..38814581-chr2:38964015..38965559,2	K562	blood:
26	chr2:38764868..38766444-chr2:38970080..38972434,2	K562	blood:
27	chr2:38754021..38756013-chr2:38969685..38972568,2	K562	blood:
28	chr2:38968077..38970035-chr2:38995563..38997615,2	K562	blood:
29	chr2:38539761..38541976-chr2:38970662..38973423,3	K562	blood:
30	chr2:38806174..38811270-chr2:38966687..38973672,10	K562	blood:
31	chr2:38816516..38836019-chr2:38963690..38980163,62	K562	blood:
32	chr2:38761614..38763492-chr2:38966918..38968538,2	K562	blood:
33	chr2:38783818..38787523-chr2:38967718..38971056,4	K562	blood:
34	chr2:38748674..38751613-chr2:38962125..38964989,2	K562	blood:
35	chr2:38824669..38828895-chr2:38950792..38955552,5	K562	blood:
36	chr2:38830274..38832898-chr2:38967361..38970126,3	K562	blood:
37	chr2:38949315..38952552-chr2:38977196..38979499,3	K562	blood:
38	chr2:38968273..38972141-chr2:39003625..39007051,4	MCF-7	breast:
39	chr2:38827236..38831286-chr2:38946528..38952512,8	K562	blood:
40	chr2:38803779..38806486-chr2:38953077..38954678,2	MCF-7	breast:
41	chr2:38806614..38812442-chr2:38966843..38970976,5	K562	blood:
42	chr2:38958596..38960601-chr2:38963108..38966299,3	K562	blood:
43	chr2:38824718..38826820-chr2:38951264..38953232,2	K562	blood:
44	chr2:38828482..38830081-chr2:38959059..38962249,3	MCF-7	breast:
45	chr2:38807538..38810280-chr2:38962388..38964852,2	K562	blood:
46	chr2:38968377..38971030-chr2:39036081..39038951,2	K562	blood:
47	chr2:38754116..38756013-chr2:38969900..38972568,2	K562	blood:
48	chr2:38776554..38778945-chr2:38971889..38973441,2	K562	blood:
49	chr2:38521502..38523654-chr2:38961697..38963293,2	K562	blood:
50	chr2:38957599..38960532-chr2:38963906..38966818,3	MCF-7	breast:

No data

(count:12 , 50 per page) page: 1

No.	miRNA target gene	miRNA name	Chromosome Location
1	SRSF7	hsa-miR-421	chr2:38972112-38972106
2	SFRS7	hsa-miR-374b-5p	chr2:38972223-38972244
3	SRSF7	hsa-miR-181a-5p	chr2:38972109-38972102
4	SFRS7	hsa-miR-130b-3p	chr2:38970816-38970838
5	SFRS7	hsa-miR-374b-5p	chr2:38972118-38972140
6	SRSF7	hsa-miR-130b-3p	chr2:38970822-38970816
7	SFRS7	hsa-miR-130b-3p	chr2:38971609-38971632
8	SFRS7	hsa-miR-181a-5p	chr2:38972103-38972125
9	SRSF7	hsa-miR-374b-5p	chr2:38972229-38972222
10	SFRS7	hsa-miR-421	chr2:38970819-38970838
11	SFRS7	hsa-miR-421	chr2:38972107-38972130
12	SFRS7	hsa-miR-22-3p	chr2:38970833-38970855

Variant related genes	Relation type
GEMIN6	TF binding region
GEMIN6	CpG island
ENSG00000119787	chromatin interactions
ENSG00000188010	chromatin interactions
ENSG00000271443	chromatin interactions
ENSG00000152147	chromatin interactions
ENSG00000143891	chromatin interactions
ENSG00000235586	chromatin interactions
ENSG00000227238	chromatin interactions
ENSG00000232114	chromatin interactions
ENSG00000223922	chromatin interactions
ENSG00000143889	chromatin interactions
ENSG00000163214	chromatin interactions
ENSG00000115875	chromatin interactions

Extended variants
information (count: 1073 )
Associated
traits (count: 61 )

Variant overlapped rSNPs/rCNVs (count:1073 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs552604011	chr2:38951654-38951655	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
2	rs1997377	chr2:38951666-38951667	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
3	rs368246935	chr2:38951680-38951681	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
4	rs565211675	chr2:38951681-38951682	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
5	rs538303481	chr2:38951723-38951724	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
6	rs146795729	chr2:38951751-38951752	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
7	rs551839230	chr2:38951776-38951777	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
8	rs201340639	chr2:38951834-38951835	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
9	rs115014586	chr2:38951937-38951938	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
10	rs536025449	chr2:38951950-38951951	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
11	rs554201863	chr2:38951963-38951964	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
12	rs140494653	chr2:38952028-38952029	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
13	rs115608560	chr2:38952048-38952049	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
14	rs79324535	chr2:38952074-38952075	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
15	rs75150586	chr2:38952081-38952082	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
16	rs543076836	chr2:38952089-38952090	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
17	rs561802239	chr2:38952239-38952240	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
18	rs565534492	chr2:38952284-38952285	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
19	rs573791086	chr2:38952295-38952296	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
20	rs55750629	chr2:38952306-38952307	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
21	rs35270252	chr2:38952318-38952319	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
22	rs146635174	chr2:38952408-38952409	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
23	rs559437445	chr2:38952424-38952425	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
24	rs369477554	chr2:38952488-38952489	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
25	rs533216783	chr2:38952595-38952596	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
26	rs141074430	chr2:38952636-38952637	Weak transcription Enhancers Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
27	rs564440592	chr2:38952654-38952655	Weak transcription Enhancers Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
28	rs372977323	chr2:38952655-38952656	Weak transcription Enhancers Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
29	rs10201210	chr2:38952667-38952668	Weak transcription Enhancers Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
30	rs375841134	chr2:38952669-38952670	Weak transcription Enhancers Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
31	rs3112141	chr2:38952673-38952674	Weak transcription Enhancers Strong transcription	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs142684432	chr2:38952689-38952690	Weak transcription Enhancers Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
33	rs112827171	chr2:38952691-38952692	Weak transcription Enhancers Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
34	rs34350782	chr2:38952692-38952693	Weak transcription Enhancers Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
35	rs373831260	chr2:38952693-38952694	Weak transcription Enhancers Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
36	rs568525800	chr2:38952697-38952698	Weak transcription Enhancers Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
37	rs188423752	chr2:38952707-38952708	Weak transcription Enhancers Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
38	rs376401856	chr2:38952708-38952709	Weak transcription Enhancers Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
39	rs369241371	chr2:38952709-38952710	Weak transcription Enhancers Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
40	rs547965440	chr2:38952748-38952749	Weak transcription Enhancers Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
41	rs114774838	chr2:38952790-38952791	Weak transcription Enhancers Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
42	rs539701783	chr2:38952798-38952799	Weak transcription Enhancers Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
43	rs142522432	chr2:38952811-38952812	Weak transcription Enhancers Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
44	rs28412370	chr2:38952848-38952849	Weak transcription Enhancers Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
45	rs557344555	chr2:38952909-38952910	Weak transcription Enhancers Strong transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
46	rs138876003	chr2:38952930-38952931	Weak transcription Enhancers Strong transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
47	rs536638109	chr2:38952946-38952947	Weak transcription Enhancers Strong transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
48	rs3112144	chr2:38953000-38953001	Weak transcription Enhancers Strong transcription	Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs369191040	chr2:38953010-38953011	Weak transcription Enhancers Strong transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
50	rs573680055	chr2:38953037-38953038	Weak transcription Enhancers Strong transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:61)

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
T-cell lymphomas	22341440	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:968 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:38894400-38960600	Weak transcription	Brain Substantia Nigra	brain
2	chr2:38909400-38960600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
3	chr2:38918600-38956800	Weak transcription	Sigmoid Colon	Sigmoid Colon
4	chr2:38927600-38957000	Weak transcription	Brain Hippocampus Middle	brain
5	chr2:38928800-38971600	Weak transcription	Small Intestine	intestine
6	chr2:38930000-38956600	Weak transcription	Rectal Mucosa Donor 31	rectum
7	chr2:38930600-38965000	Weak transcription	Gastric	stomach
8	chr2:38932800-38956800	Weak transcription	Brain Inferior Temporal Lobe	brain
9	chr2:38936400-38957200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
10	chr2:38936400-38960600	Weak transcription	H9 Cell Line	embryonic stem cell
11	chr2:38936400-38968400	Weak transcription	Colonic Mucosa	Colon
12	chr2:38937200-38956600	Weak transcription	Fetal Brain Female	brain
13	chr2:38937600-38970400	Weak transcription	Placenta Amnion	Placenta Amnion
14	chr2:38939000-38956600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
15	chr2:38939200-38958600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
16	chr2:38943600-38956000	Weak transcription	Rectal Mucosa Donor 29	rectum
17	chr2:38943600-38958600	Weak transcription	Aorta	Aorta
18	chr2:38946400-38957000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
19	chr2:38947800-38953200	Enhancers	Primary T helper cells fromperipheralblood	blood
20	chr2:38948000-38952400	Weak transcription	HepG2	liver
21	chr2:38948000-38953400	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
22	chr2:38948000-38955800	Weak transcription	Fetal Intestine Large	intestine
23	chr2:38948000-38958600	Weak transcription	Cortex derived primary cultured neurospheres	brain
24	chr2:38948200-38956600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
25	chr2:38948200-38956600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
26	chr2:38948200-38956600	Weak transcription	Rectal Smooth Muscle	rectum
27	chr2:38948200-38957000	Weak transcription	Spleen	Spleen
28	chr2:38948200-38958600	Weak transcription	Esophagus	oesophagus
29	chr2:38948200-38968200	Weak transcription	Stomach Mucosa	stomach
30	chr2:38948400-38952800	Weak transcription	K562	blood
31	chr2:38948400-38956600	Weak transcription	HUES6 Cell Line	embryonic stem cell
32	chr2:38948400-38958600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
33	chr2:38948400-38958800	Weak transcription	Colon Smooth Muscle	Colon
34	chr2:38948400-38964400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
35	chr2:38948400-38964600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
36	chr2:38948400-38970600	Weak transcription	NHEK	skin
37	chr2:38948600-38956600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
38	chr2:38948600-38956800	Weak transcription	Brain Anterior Caudate	brain
39	chr2:38948600-38957000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
40	chr2:38948600-38959600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
41	chr2:38948600-38970200	Weak transcription	NHDF-Ad	bronchial
42	chr2:38948600-38971200	Weak transcription	Fetal Kidney	kidney
43	chr2:38948800-38956600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
44	chr2:38948800-38956600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
45	chr2:38948800-38956800	Weak transcription	Brain Cingulate Gyrus	brain
46	chr2:38948800-38957000	Weak transcription	Lung	lung
47	chr2:38948800-38960200	Weak transcription	Hela-S3	cervix
48	chr2:38948800-38960600	Weak transcription	Brain Angular Gyrus	brain
49	chr2:38948800-38964600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
50	chr2:38949000-38956800	Weak transcription	Ovary	ovary

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