Variant report

Variant	esv2763640
Chromosome Location	chr2:38954419-38977371
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1112)
CpG islands
(count:366)
Chromatin interactive
region (count:117)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:12)

(count:1112 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

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	chr2:38958825-38959337	HepG2	liver:	n/a	n/a
3	ARID3A	chr2:38968049-38968417	HepG2	liver:	n/a	n/a
4	ARID3A	chr2:38960583-38960998	HepG2	liver:	n/a	n/a
5	ARID3A	chr2:38957567-38957767	HepG2	liver:	n/a	n/a
6	ARID3A	chr2:38969026-38969567	HepG2	liver:	n/a	n/a
7	ATF2	chr2:38975924-38976359	H1-hESC	embryonic stem cell:	n/a	n/a
8	ATF2	chr2:38971052-38971500	H1-hESC	embryonic stem cell:	n/a	n/a
9	ATF2	chr2:38976904-38977503	H1-hESC	embryonic stem cell:	n/a	n/a
10	ATF2	chr2:38970329-38971016	H1-hESC	embryonic stem cell:	n/a	n/a
11	ATF2	chr2:38969791-38970170	H1-hESC	embryonic stem cell:	n/a	n/a
12	ATF3	chr2:38966713-38966989	K562	blood:	n/a	n/a
13	BACH1	chr2:38974736-38974871	K562	blood:	n/a	n/a
14	BACH1	chr2:38976689-38978674	K562	blood:	n/a	n/a
15	BCL3	chr2:38968167-38968631	A549	lung:	n/a	n/a
16	BCL3	chr2:38970314-38970670	K562	blood:	n/a	n/a
17	BCL3	chr2:38970620-38971557	A549	lung:	n/a	n/a
18	BCL3	chr2:38969826-38970596	A549	lung:	n/a	n/a
19	BCL3	chr2:38970097-38971823	K562	blood:	n/a	n/a
20	BCL3	chr2:38967993-38968638	A549	lung:	n/a	n/a
21	BCLAF1	chr2:38969877-38971863	K562	blood:	n/a	n/a
22	BCLAF1	chr2:38969857-38970244	GM12878	blood:	n/a	n/a
23	BCLAF1	chr2:38970745-38971762	K562	blood:	n/a	n/a
24	BCLAF1	chr2:38977246-38978879	GM12878	blood:	n/a	chr2:38977752-38977761 chr2:38977730-38977743 chr2:38978222-38978231
25	BCLAF1	chr2:38969864-38970331	GM12878	blood:	n/a	n/a
26	BHLHE40	chr2:38970388-38970677	K562	blood:	n/a	n/a
27	BHLHE40	chr2:38976783-38976828	HepG2	liver:	n/a	n/a
28	BHLHE40	chr2:38957732-38957923	HepG2	liver:	n/a	n/a
29	BHLHE40	chr2:38976741-38976822	K562	blood:	n/a	n/a
30	BHLHE40	chr2:38976277-38976859	GM12878	blood:	n/a	n/a
31	BRCA1	chr2:38976139-38976194	GM12878	blood:	n/a	n/a
32	BRCA1	chr2:38968158-38968358	Hela-S3	cervix:	n/a	n/a
33	CBX3	chr2:38966627-38967081	K562	blood:	n/a	n/a
34	CBX3	chr2:38967982-38968397	K562	blood:	n/a	n/a
35	CBX3	chr2:38966528-38967101	K562	blood:	n/a	n/a
36	CCNT2	chr2:38970132-38970513	K562	blood:	n/a	n/a
37	CEBPB	chr2:38964265-38964887	ECC-1	luminal epithelium:	n/a	n/a
38	CEBPB	chr2:38970095-38970305	H1-hESC	embryonic stem cell:	n/a	chr2:38970222-38970233
39	CEBPB	chr2:38970089-38970536	IMR90	lung:	n/a	chr2:38970438-38970449 chr2:38970222-38970233
40	CEBPB	chr2:38964006-38964062	K562	blood:	n/a	n/a
41	CEBPB	chr2:38970063-38970499	K562	blood:	n/a	chr2:38970438-38970449 chr2:38970222-38970233
42	CEBPB	chr2:38964278-38964893	ECC-1	luminal epithelium:	n/a	n/a
43	CEBPB	chr2:38971156-38971289	K562	blood:	n/a	n/a
44	CEBPB	chr2:38970114-38970254	HepG2	liver:	n/a	chr2:38970222-38970233
45	CEBPB	chr2:38974499-38974719	IMR90	lung:	n/a	n/a
46	CEBPB	chr2:38977274-38978779	Hela-S3	cervix:	n/a	n/a
47	CEBPB	chr2:38970072-38970600	A549	lung:	n/a	chr2:38970438-38970449 chr2:38970222-38970233
48	CEBPB	chr2:38960788-38961059	HepG2	liver:	n/a	n/a
49	CEBPB	chr2:38974466-38974756	K562	blood:	n/a	n/a
50	CEBPB	chr2:38969926-38970577	K562	blood:	n/a	chr2:38970438-38970449 chr2:38970222-38970233

(count:366 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:38970936-38970986	SKMC	muscle:	n/a
2	chr2:38961590-38961640	HMEC	breast:	n/a
3	chr2:38961590-38961640	NT2-D1	testis:	n/a
4	chr2:38976250-38976300	HPAEpiC	pulmonary alveolar:	n/a
5	chr2:38961590-38961640	SK-N-SH	brain:	n/a
6	chr2:38970936-38970986	BE2_C	brain:	n/a
7	chr2:38970936-38970986	ProgFib	skin:	n/a
8	chr2:38970936-38970986	Hepatocyte	liver:	n/a
9	chr2:38976250-38976300	NB4	blood:	n/a
10	chr2:38976288-38976338	PFSK-1	brain:	n/a
11	chr2:38970936-38970986	HRE	kidney:	n/a
12	chr2:38976250-38976300	H1-hESC	embryonic stem cell:	embryo
13	chr2:38976409-38976459	H1-hESC	embryonic stem cell:	embryo
14	chr2:38977301-38977351	HRPEpiC	eye:	n/a
15	chr2:38961590-38961640	IMR90	lung:	fetal
16	chr2:38977301-38977351	HNPCEpiC	eye:	n/a
17	chr2:38976250-38976300	GM19239	blood:	n/a
18	chr2:38976250-38976300	ovcar-3	ovarian:	n/a
19	chr2:38976250-38976300	HCF	heart:	n/a
20	chr2:38976288-38976338	HCPEpiC	choroid plexus:	n/a
21	chr2:38970936-38970986	ECC-1	luminal epithelium:	n/a
22	chr2:38970936-38970986	NH-A	brain:	n/a
23	chr2:38976250-38976300	ProgFib	skin:	n/a
24	chr2:38970936-38970986	GM12891	blood:	n/a
25	chr2:38977301-38977351	AoSMC	blood vessel:	n/a
26	chr2:38976288-38976338	AG04450	lung:	fetal
27	chr2:38977301-38977351	GM19239	blood:	n/a
28	chr2:38976409-38976459	MCF-7	breast:	n/a
29	chr2:38970936-38970986	AG04450	lung:	fetal
30	chr2:38970936-38970986	SK-N-MC	brain:	n/a
31	chr2:38976288-38976338	HRPEpiC	eye:	n/a
32	chr2:38961590-38961640	RPTEC	kidney:	n/a
33	chr2:38961590-38961640	SK-N-SH_RA	brain:	n/a
34	chr2:38976409-38976459	Hepatocyte	liver:	n/a
35	chr2:38976288-38976338	HRE	kidney:	n/a
36	chr2:38976250-38976300	SKMC	muscle:	n/a
37	chr2:38976250-38976300	NHDF-neo	bronchial:	n/a
38	chr2:38976288-38976338	HPAEpiC	pulmonary alveolar:	n/a
39	chr2:38970936-38970986	U87	brain:	n/a
40	chr2:38976409-38976459	GM06990	blood:	n/a
41	chr2:38976288-38976338	NT2-D1	testis:	n/a
42	chr2:38976409-38976459	HPAEpiC	pulmonary alveolar:	n/a
43	chr2:38976250-38976300	NT2-D1	testis:	n/a
44	chr2:38976288-38976338	HUVEC	blood vessel:	n/a
45	chr2:38976409-38976459	ProgFib	skin:	n/a
46	chr2:38976409-38976459	T-47D	breast:	n/a
47	chr2:38977301-38977351	RPTEC	kidney:	n/a
48	chr2:38976250-38976300	HCM	heart:	n/a
49	chr2:38976288-38976338	HRCEpiC	kidney:	n/a
50	chr2:38976409-38976459	AG04450	lung:	fetal

(count:117 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr2:38800582..38805538-chr2:38967531..38972325,7	K562	blood:
2	chr2:38970433..38973202-chr2:39101561..39103426,2	K562	blood:
3	chr2:38977048..38979806-chr2:39045778..39047764,3	MCF-7	breast:
4	chr2:38974982..38979904-chr2:39002191..39014206,31	MCF-7	breast:
5	chr2:38764868..38766444-chr2:38970080..38972434,2	K562	blood:
6	chr2:38539761..38541976-chr2:38970662..38973423,2	K562	blood:
7	chr2:38966114..38968421-chr2:39005419..39007550,2	MCF-7	breast:
8	chr2:38973415..38975366-chr2:39100938..39103537,2	K562	blood:
9	chr2:37457826..37459742-chr2:38976926..38979723,2	K562	blood:
10	chr2:38742460..38744108-chr2:38976998..38978688,2	MCF-7	breast:
11	chr2:38968077..38970035-chr2:38995563..38997615,2	K562	blood:
12	chr2:38825865..38831347-chr2:38967441..38973263,7	MCF-7	breast:
13	chr2:38968377..38971030-chr2:39036081..39038951,2	K562	blood:
14	chr2:38977033..38979904-chr2:47402717..47404547,2	K562	blood:
15	chr2:38760428..38762981-chr2:38976976..38979591,3	K562	blood:
16	chr19:5689960..5691696-chr2:38976849..38978490,2	K562	blood:
17	chr2:38948167..38950183-chr2:38951156..38954719,3	MCF-7	breast:
18	chr2:38763105..38763665-chr2:38968175..38968815,2	MCF-7	breast:
19	chr2:38976573..38978521-chr7:139025166..139027666,2	MCF-7	breast:
20	chr2:38776916..38778592-chr2:38969344..38970967,2	K562	blood:
21	chr2:38977319..38978523-chr5:32312613..32313523,3	Hela-S3	cervix:
22	chr2:38824074..38831950-chr2:38975822..38980618,12	MCF-7	breast:
23	chr2:38749544..38751613-chr2:38963489..38965052,2	K562	blood:
24	chr2:38890926..38894484-chr2:38966717..38969696,3	K562	blood:
25	chr2:38759757..38767880-chr2:38967038..38973617,12	K562	blood:
26	chr2:38601699..38605766-chr2:38977040..38979128,3	MCF-7	breast:
27	chr2:38977028..38978558-chr3:149686195..149689135,2	MCF-7	breast:
28	chr2:38973025..38976072-chr2:38989424..38992491,3	MCF-7	breast:
29	chr2:38976218..38980921-chr2:39003670..39007764,15	K562	blood:
30	chr2:38952964..38955147-chr2:38962662..38964178,2	K562	blood:
31	chr2:38976457..38978515-chr2:39347011..39349138,2	K562	blood:
32	chr2:38762042..38765801-chr2:38976684..38979922,4	MCF-7	breast:
33	chr2:38892007..38895113-chr2:38976994..38979857,4	K562	blood:
34	chr2:38957599..38960532-chr2:38963906..38966818,3	MCF-7	breast:
35	chr18:77866823..77867548-chr2:38977208..38978100,2	Hela-S3	cervix:
36	chr2:38976877..38979785-chr2:39100480..39105632,13	K562	blood:
37	chr2:38976891..38979056-chr2:39028521..39033921,5	MCF-7	breast:
38	chr2:38806614..38812442-chr2:38966843..38970976,5	K562	blood:
39	chr2:38761989..38764024-chr2:38963798..38966475,2	K562	blood:
40	chr2:38891654..38895079-chr2:38966717..38969696,3	K562	blood:
41	chr2:38819128..38833161-chr2:38974716..38980003,37	K562	blood:
42	chr2:38778308..38780052-chr2:38967008..38969234,2	K562	blood:
43	chr2:38977027..38978972-chr2:39249720..39251575,2	K562	blood:
44	chr2:38975535..38978590-chr2:39035789..39038871,3	MCF-7	breast:
45	chr15:72409880..72410484-chr2:38976828..38977720,2	Hela-S3	cervix:
46	chr2:38975839..38978922-chr2:47400598..47403972,4	K562	blood:
47	chr2:38776554..38778945-chr2:38971889..38973441,2	K562	blood:
48	chr2:38812622..38815204-chr2:38976239..38979096,3	K562	blood:
49	chr2:38842870..38845739-chr2:38968254..38970613,2	K562	blood:
50	chr2:38976938..38979508-chr2:39454441..39457000,2	K562	blood:

No data

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

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

Variant related genes	Relation type
GEMIN6	TF binding region
SRSF7	TF binding region
GEMIN6	CpG island
SRSF7	CpG island
ENSG00000143891	chromatin interactions
ENSG00000223922	chromatin interactions
ENSG00000231367	chromatin interactions
ENSG00000168298	chromatin interactions
ENSG00000163214	chromatin interactions
ENSG00000212628	chromatin interactions
ENSG00000164898	chromatin interactions
ENSG00000070087	chromatin interactions
ENSG00000269955	chromatin interactions
ENSG00000235586	chromatin interactions
ENSG00000120738	chromatin interactions
ENSG00000130255	chromatin interactions
ENSG00000143889	chromatin interactions
ENSG00000138061	chromatin interactions
ENSG00000010626	chromatin interactions
ENSG00000150712	chromatin interactions
ENSG00000227238	chromatin interactions
ENSG00000268175	chromatin interactions
ENSG00000168906	chromatin interactions
ENSG00000101544	chromatin interactions
ENSG00000205111	chromatin interactions
ENSG00000232114	chromatin interactions
ENSG00000119787	chromatin interactions
ENSG00000003509	chromatin interactions
ENSG00000271443	chromatin interactions
ENSG00000115875	chromatin interactions
ENSG00000233396	chromatin interactions
ENSG00000158373	chromatin interactions
ENSG00000232973	chromatin interactions
ENSG00000168993	chromatin interactions
ENSG00000201558	chromatin interactions
ENSG00000188010	chromatin interactions
ENSG00000115816	chromatin interactions
ENSG00000115904	chromatin interactions
ENSG00000143933	chromatin interactions
ENSG00000165416	chromatin interactions
ENSG00000152147	chromatin interactions
ENSG00000066933	chromatin interactions

Extended variants
information (count: 1177 )
Associated
traits (count: 61 )

Variant overlapped rSNPs/rCNVs (count:1177 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11124646	chr2:38954419-38954420	Weak transcription Enhancers Strong transcription	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs532611907	chr2:38954490-38954491	Weak transcription Enhancers Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs545208044	chr2:38954505-38954506	Weak transcription Enhancers Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs547672860	chr2:38954565-38954566	Weak transcription Enhancers Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs181293546	chr2:38954593-38954594	Weak transcription Enhancers Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs138939314	chr2:38954600-38954601	Weak transcription Enhancers Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs560001464	chr2:38954608-38954609	Weak transcription Enhancers Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs112066395	chr2:38954619-38954620	Weak transcription Enhancers Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs561407800	chr2:38954644-38954645	Weak transcription Enhancers Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs529608753	chr2:38954653-38954654	Weak transcription Enhancers Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs546615669	chr2:38954666-38954667	Weak transcription Enhancers Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs571367002	chr2:38954675-38954676	Weak transcription Enhancers Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs375328583	chr2:38954711-38954712	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs538695802	chr2:38954762-38954763	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs548190042	chr2:38954764-38954765	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs149978657	chr2:38954810-38954811	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs569004862	chr2:38954822-38954823	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs3112156	chr2:38954865-38954866	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs565518448	chr2:38954867-38954868	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs79988749	chr2:38954868-38954869	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs185599245	chr2:38954879-38954880	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs573053404	chr2:38954909-38954910	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs535024420	chr2:38954958-38954959	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs189912817	chr2:38955044-38955045	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs139136169	chr2:38955115-38955116	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs545072752	chr2:38955116-38955117	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs7603676	chr2:38955129-38955130	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
28	rs6727533	chr2:38955153-38955154	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs149807829	chr2:38955168-38955169	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs146330536	chr2:38955176-38955177	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs570658337	chr2:38955202-38955203	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs567001956	chr2:38955206-38955207	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs528731214	chr2:38955219-38955220	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs7603821	chr2:38955258-38955259	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
35	rs386645149	chr2:38955261-38955262	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs532264789	chr2:38955345-38955346	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs189911638	chr2:38955365-38955366	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs182240059	chr2:38955419-38955420	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs369881625	chr2:38955426-38955427	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs7604054	chr2:38955451-38955452	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs553746583	chr2:38955455-38955456	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs7604132	chr2:38955468-38955469	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs548035273	chr2:38955472-38955473	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs373566678	chr2:38955525-38955526	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs377334655	chr2:38955527-38955528	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs528393893	chr2:38955534-38955535	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs11464719	chr2:38955535-38955536	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs200016092	chr2:38955544-38955545	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs397943735	chr2:38955546-38955547	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs200412595	chr2:38955547-38955548	Weak transcription	Chromatin interactive region	2 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:1278 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

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	chr2:38948000-38955800	Weak transcription	Fetal Intestine Large	intestine
20	chr2:38948000-38958600	Weak transcription	Cortex derived primary cultured neurospheres	brain
21	chr2:38948200-38956600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
22	chr2:38948200-38956600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
23	chr2:38948200-38956600	Weak transcription	Rectal Smooth Muscle	rectum
24	chr2:38948200-38957000	Weak transcription	Spleen	Spleen
25	chr2:38948200-38958600	Weak transcription	Esophagus	oesophagus
26	chr2:38948200-38968200	Weak transcription	Stomach Mucosa	stomach
27	chr2:38948400-38956600	Weak transcription	HUES6 Cell Line	embryonic stem cell
28	chr2:38948400-38958600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
29	chr2:38948400-38958800	Weak transcription	Colon Smooth Muscle	Colon
30	chr2:38948400-38964400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
31	chr2:38948400-38964600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
32	chr2:38948400-38970600	Weak transcription	NHEK	skin
33	chr2:38948600-38956600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
34	chr2:38948600-38956800	Weak transcription	Brain Anterior Caudate	brain
35	chr2:38948600-38957000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
36	chr2:38948600-38959600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
37	chr2:38948600-38970200	Weak transcription	NHDF-Ad	bronchial
38	chr2:38948600-38971200	Weak transcription	Fetal Kidney	kidney
39	chr2:38948800-38956600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
40	chr2:38948800-38956600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
41	chr2:38948800-38956800	Weak transcription	Brain Cingulate Gyrus	brain
42	chr2:38948800-38957000	Weak transcription	Lung	lung
43	chr2:38948800-38960200	Weak transcription	Hela-S3	cervix
44	chr2:38948800-38960600	Weak transcription	Brain Angular Gyrus	brain
45	chr2:38948800-38964600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
46	chr2:38949000-38956800	Weak transcription	Ovary	ovary
47	chr2:38949000-38958600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
48	chr2:38949000-38965000	Weak transcription	Right Ventricle	heart
49	chr2:38949600-38956800	Weak transcription	Osteobl	bone
50	chr2:38949800-38956600	Weak transcription	Adipose Nuclei	Adipose

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