Variant report

Variant	nsv874278
Chromosome Location	chr2:73870010-73931971
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:959)
CpG islands
(count:1161)
Chromatin interactive
region (count:19)
LncRNA
region (count:8)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:959 , 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	chr2:73869857-73870120	HepG2	liver:	n/a	n/a
2	ARID3A	chr2:73907394-73907641	K562	blood:	n/a	n/a
3	ARID3A	chr2:73907372-73907682	HepG2	liver:	n/a	n/a
4	ATF1	chr2:73928292-73928546	K562	blood:	n/a	n/a
5	ATF2	chr2:73901924-73902346	GM12878	blood:	n/a	n/a
6	ATF3	chr2:73903390-73903706	K562	blood:	n/a	n/a
7	BACH1	chr2:73907465-73907526	H1-hESC	embryonic stem cell:	n/a	n/a
8	BATF	chr2:73911582-73911820	GM12878	blood:	n/a	chr2:73911707-73911718
9	BATF	chr2:73901924-73902350	GM12878	blood:	n/a	n/a
10	BATF	chr2:73901777-73902343	GM12878	blood:	n/a	n/a
11	BATF	chr2:73917830-73918048	GM12878	blood:	n/a	n/a
12	BCL11A	chr2:73901938-73902290	GM12878	blood:	n/a	chr2:73902211-73902220 chr2:73902210-73902219
13	BCL11A	chr2:73915732-73916019	GM12878	blood:	n/a	n/a
14	BHLHE40	chr2:73871815-73871977	K562	blood:	n/a	n/a
15	BHLHE40	chr2:73928154-73928613	K562	blood:	n/a	n/a
16	BHLHE40	chr2:73917955-73917976	K562	blood:	n/a	n/a
17	CBX3	chr2:73928047-73928946	K562	blood:	n/a	n/a
18	CBX3	chr2:73925299-73925547	K562	blood:	n/a	n/a
19	CBX3	chr2:73925209-73925579	K562	blood:	n/a	n/a
20	CEBPB	chr2:73903414-73903663	A549	lung:	n/a	chr2:73903539-73903550
21	CEBPB	chr2:73877771-73878092	Hela-S3	cervix:	n/a	n/a
22	CEBPB	chr2:73869936-73870184	HepG2	liver:	n/a	n/a
23	CEBPB	chr2:73900813-73900977	K562	blood:	n/a	chr2:73900873-73900886
24	CEBPB	chr2:73927189-73927886	MCF-7	breast:	n/a	chr2:73927522-73927535
25	CEBPB	chr2:73903437-73903637	H1-hESC	embryonic stem cell:	n/a	chr2:73903539-73903550
26	CEBPB	chr2:73903369-73903615	HepG2	liver:	n/a	chr2:73903539-73903550
27	CEBPB	chr2:73903410-73903643	K562	blood:	n/a	chr2:73903539-73903550
28	CEBPB	chr2:73900871-73900878	A549	lung:	n/a	n/a
29	CEBPB	chr2:73903402-73903602	Hela-S3	cervix:	n/a	chr2:73903539-73903550
30	CEBPB	chr2:73877646-73878600	HepG2	liver:	n/a	chr2:73878449-73878460
31	CEBPB	chr2:73877660-73878170	IMR90	lung:	n/a	n/a
32	CEBPB	chr2:73877667-73878169	A549	lung:	n/a	n/a
33	CEBPB	chr2:73903357-73903734	K562	blood:	n/a	chr2:73903539-73903550
34	CEBPB	chr2:73926566-73926627	A549	lung:	n/a	n/a
35	CEBPB	chr2:73927361-73927552	HepG2	liver:	n/a	chr2:73927522-73927535
36	CEBPB	chr2:73903375-73903643	IMR90	lung:	n/a	chr2:73903539-73903550
37	CEBPB	chr2:73877993-73878055	K562	blood:	n/a	n/a
38	CEBPB	chr2:73903365-73903683	K562	blood:	n/a	chr2:73903539-73903550
39	CEBPB	chr2:73927206-73927852	MCF-7	breast:	n/a	chr2:73927522-73927535
40	CHD2	chr2:73869804-73870074	HepG2	liver:	n/a	n/a
41	CTCF	chr2:73917883-73918111	H1-hESC	embryonic stem cell:	n/a	chr2:73917996-73918014 chr2:73917998-73918019 chr2:73917997-73918013 chr2:73918001-73918009 chr2:73917999-73918012
42	CTCF	chr2:73907640-73907790	GM12875	blood:	n/a	n/a
43	CTCF	chr2:73874960-73875110	RPTEC	kidney:	n/a	n/a
44	CTCF	chr2:73907240-73907390	AG09309	skin:	n/a	n/a
45	CTCF	chr2:73912260-73912410	SAEC	small airway:	n/a	n/a
46	CTCF	chr2:73912180-73912330	HFF-Myc	foreskin:	n/a	n/a
47	CTCF	chr2:73907415-73907630	MCF-7	breast:	n/a	chr2:73907497-73907513 chr2:73907499-73907512 chr2:73907498-73907519 chr2:73907496-73907514
48	CTCF	chr2:73907409-73907614	GM19239	blood:	n/a	chr2:73907497-73907513 chr2:73907499-73907512 chr2:73907498-73907519 chr2:73907496-73907514
49	CTCF	chr2:73917924-73918088	H1-hESC	embryonic stem cell:	n/a	chr2:73917996-73918014 chr2:73917998-73918019 chr2:73917997-73918013 chr2:73918001-73918009 chr2:73917999-73918012
50	CTCF	chr2:73907420-73907570	HRE	kidney:	n/a	chr2:73907497-73907513 chr2:73907499-73907512 chr2:73907498-73907519 chr2:73907496-73907514

(count:1161 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:73871942-73871992	BJ	skin:	n/a
2	chr2:73871855-73871905	AG09309	skin:	n/a
3	chr2:73871942-73871992	BJ	skin:	n/a
4	chr2:73871855-73871905	AG09309	skin:	n/a
5	chr2:73870653-73870703	U87	brain:	n/a
6	chr2:73871942-73871992	HL-60	blood:	n/a
7	chr2:73869966-73870016	GM06990	blood:	n/a
8	chr2:73871849-73871899	HEK293	kidney:	embryo
9	chr2:73870653-73870703	PFSK-1	brain:	n/a
10	chr2:73907327-73907377	ovcar-3	ovarian:	n/a
11	chr2:73929765-73929815	K562	blood:	n/a
12	chr2:73870294-73870344	MCF-7	breast:	n/a
13	chr2:73871309-73871359	HRPEpiC	eye:	n/a
14	chr2:73871309-73871359	NHBE	bronchial:	n/a
15	chr2:73870105-73870155	HepG2	liver:	n/a
16	chr2:73928348-73928398	HRPEpiC	eye:	n/a
17	chr2:73871942-73871992	AG10803	skin:	n/a
18	chr2:73928500-73928550	HL-60	blood:	n/a
19	chr2:73928348-73928398	AG04449	skin:	fetal
20	chr2:73929892-73929942	CMK	blood:	n/a
21	chr2:73871230-73871280	Hela-S3	cervix:	n/a
22	chr2:73871782-73871832	Caco-2	colon:	n/a
23	chr2:73871915-73871965	HCM	heart:	n/a
24	chr2:73929892-73929942	GM19239	blood:	n/a
25	chr2:73927710-73927760	HMEC	breast:	n/a
26	chr2:73871942-73871992	BE2_C	brain:	n/a
27	chr2:73928348-73928398	HEEpiC	esophagus:	n/a
28	chr2:73871915-73871965	GM12892	blood:	n/a
29	chr2:73927710-73927760	HEEpiC	esophagus:	n/a
30	chr2:73928492-73928542	CMK	blood:	n/a
31	chr2:73871942-73871992	GM12892	blood:	n/a
32	chr2:73929892-73929942	Hepatocyte	liver:	n/a
33	chr2:73871855-73871905	RPTEC	kidney:	n/a
34	chr2:73929765-73929815	GM12891	blood:	n/a
35	chr2:73870105-73870155	HCM	heart:	n/a
36	chr2:73871849-73871899	PFSK-1	brain:	n/a
37	chr2:73871849-73871899	HPAEpiC	pulmonary alveolar:	n/a
38	chr2:73871942-73871992	IMR90	lung:	fetal
39	chr2:73928492-73928542	AG10803	skin:	n/a
40	chr2:73870653-73870703	AG09319	gingival:	n/a
41	chr2:73870294-73870344	GM12891	blood:	n/a
42	chr2:73928500-73928550	T-47D	breast:	n/a
43	chr2:73928500-73928550	AG04449	skin:	fetal
44	chr2:73871309-73871359	NHDF-neo	bronchial:	n/a
45	chr2:73907327-73907377	Hela-S3	cervix:	n/a
46	chr2:73871782-73871832	SKMC	muscle:	n/a
47	chr2:73929634-73929684	GM06990	blood:	n/a
48	chr2:73928348-73928398	HUVEC	blood vessel:	n/a
49	chr2:73871942-73871992	PANC-1	pancreas:	n/a
50	chr2:73871230-73871280	LNCaP	prostate:	n/a

(count:19 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:73907051..73907568-chr2:74006793..74007607,2	MCF-7	breast:
2	chr2:73857783..73858474-chr2:73917561..73918197,2	MCF-7	breast:
3	chr2:73878117..73880708-chr2:73881565..73884435,2	K562	blood:
4	chr2:73931503..73934295-chr2:73936024..73937687,2	MCF-7	breast:
5	chr2:73927692..73931050-chr2:73931884..73934947,3	K562	blood:
6	chr2:73880223..73882700-chr2:73884731..73886778,2	K562	blood:
7	chr2:73920861..73923082-chr2:73929614..73932212,2	K562	blood:
8	chr2:73850004..73850829-chr2:73907369..73907993,2	K562	blood:
9	chr2:73878117..73880708-chr2:73881565..73884435,2	K562	blood:
10	chr2:73888338..73891192-chr2:73900081..73901857,2	K562	blood:
11	chr2:73906056..73907836-chr2:74356105..74358909,2	MCF-7	breast:
12	chr2:73880223..73882700-chr2:73884731..73886778,2	K562	blood:
13	chr2:73846810..73847325-chr2:73907451..73907990,3	K562	blood:
14	chr2:73888338..73891192-chr2:73900081..73901857,2	K562	blood:
15	chr2:73846839..73847625-chr2:73907303..73907990,2	MCF-7	breast:
16	chr2:73868945..73872912-chr2:73927731..73932752,4	MCF-7	breast:
17	chr2:73907073..73907951-chr2:74066396..74067279,2	MCF-7	breast:
18	chr2:73868945..73872912-chr2:73927731..73932752,4	MCF-7	breast:
19	chr2:73920861..73923082-chr2:73929614..73932212,2	K562	blood:

(count:8 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ALMS1-3	chr2:73900940-73901123	NR_003683
2	lnc-ALMS1-3	chr2:73872046-73872281	NR_003683
3	lnc-C2orf78-1	chr2:73927556-73928129	ENSG00000251346
4	lnc-ALMS1-3	chr2:73912088-73912694	NR_003683
5	lnc-ALMS1-3	chr2:73901969-73902032	NR_003683
6	lnc-ALMS1-3	chr2:73899935-73900177	NR_003683
7	lnc-ALMS1-3	chr2:73899436-73899622	NR_003683
8	lnc-ALMS1-3	chr2:73898207-73898277	NR_003683

No data

Variant related genes	Relation type
ALMS1P	TF binding region
ENSG00000204872	TF binding region
NAT8	TF binding region
ALMS1P	CpG island
ENSG00000204872	CpG island
NAT8	CpG island
ENSG00000144035	chromatin interactions
ENSG00000144048	chromatin interactions
ENSG00000204872	chromatin interactions
ENSG00000163016	chromatin interactions
UBE2I	miRNA target sites

Extended variants
information (count: 2306 )
Associated
traits (count: 62 )

Variant overlapped rSNPs/rCNVs (count:2306 , 50 per page) page: 1 2 3 4 5 6 7 ... 47

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4852954	chr2:73870010-73870011	ZNF genes & repeats Enhancers Flanking Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs566384203	chr2:73870028-73870029	ZNF genes & repeats Enhancers Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs533884340	chr2:73870062-73870063	ZNF genes & repeats Enhancers Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs1879661	chr2:73870071-73870072	ZNF genes & repeats Enhancers Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs555134792	chr2:73870072-73870073	ZNF genes & repeats Enhancers Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs543840678	chr2:73870074-73870075	ZNF genes & repeats Enhancers Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs543951835	chr2:73870082-73870083	ZNF genes & repeats Enhancers Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs562040480	chr2:73870105-73870106	ZNF genes & repeats Enhancers Flanking Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs192713385	chr2:73870111-73870112	ZNF genes & repeats Enhancers Flanking Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs35749858	chr2:73870143-73870144	ZNF genes & repeats Enhancers Flanking Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs397843506	chr2:73870206-73870207	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs529392923	chr2:73870210-73870211	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs2947846	chr2:73870221-73870222	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs76502288	chr2:73870234-73870235	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs527986816	chr2:73870237-73870238	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs543381355	chr2:73870263-73870264	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs561449229	chr2:73870296-73870297	Enhancers Weak transcription Flanking Active TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs531959932	chr2:73870299-73870300	Enhancers Weak transcription Flanking Active TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs375811360	chr2:73870324-73870325	Enhancers Weak transcription Flanking Active TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs571676954	chr2:73870340-73870341	Enhancers Weak transcription Flanking Active TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs532505226	chr2:73870382-73870383	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs139909119	chr2:73870515-73870516	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs565778899	chr2:73870532-73870533	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs114029547	chr2:73870573-73870574	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs555270041	chr2:73870610-73870611	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs28576012	chr2:73870697-73870698	Weak transcription Enhancers	CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs141773463	chr2:73870836-73870837	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs538011437	chr2:73870843-73870844	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs185045903	chr2:73870846-73870847	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs552083047	chr2:73870858-73870859	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs544822686	chr2:73870865-73870866	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs553793076	chr2:73870867-73870868	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs572102872	chr2:73870880-73870881	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs543318699	chr2:73870900-73870901	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs4852311	chr2:73870929-73870930	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs576677733	chr2:73870934-73870935	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs373104227	chr2:73870940-73870941	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs76220488	chr2:73870958-73870959	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs147942097	chr2:73870960-73870961	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs57018765	chr2:73870961-73870962	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs188488294	chr2:73870963-73870964	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs543951278	chr2:73870985-73870986	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs397834868	chr2:73871012-73871013	Bivalent Enhancer Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs189556640	chr2:73871019-73871020	Bivalent Enhancer Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs532632243	chr2:73871032-73871033	Bivalent Enhancer Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs547521380	chr2:73871065-73871066	Bivalent Enhancer Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs114513719	chr2:73871069-73871070	Bivalent Enhancer Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs72913482	chr2:73871076-73871077	Bivalent Enhancer Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs370916533	chr2:73871082-73871083	Bivalent Enhancer Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs567510011	chr2:73871120-73871121	Bivalent Enhancer Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:62)

Disease	PMID	Source
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
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
Hodgkin''s lymphoma	18641027	CNVD
Follicular lymphoma	20505157	CNVD
Autism	17483303	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Medulloblastoma	20607354	CNVD
Autism	22495311	CNVD
Autism	18522746	CNVD
Lung cancer	18438408	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
Developmental delay	21147756	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Seminomas	18059402	CNVD
Testicular germ cell tumor	18059402	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Hepatocellular carcinoma	16750200	CNVD
Renal cell carcinoma	18765545	CNVD
Myxofibrosarcoma	16751306	CNVD
small cell lung cancer	20016488	CNVD
Acute myeloid leukemia	21251322	CNVD
Myelofibrosis	22110671	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Melanoma	20877625	CNVD

Chromatin state (count:292 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:73866200-73870600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
2	chr2:73866400-73871200	Enhancers	Fetal Lung	lung
3	chr2:73867000-73872200	Enhancers	Ovary	ovary
4	chr2:73867400-73870200	Flanking Active TSS	Liver	Liver
5	chr2:73867400-73870200	Enhancers	Fetal Intestine Large	intestine
6	chr2:73867600-73872200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
7	chr2:73868400-73871000	Weak transcription	Spleen	Spleen
8	chr2:73868400-73871400	Enhancers	Primary hematopoietic stem cells	blood
9	chr2:73868600-73877000	Weak transcription	Gastric	stomach
10	chr2:73869000-73870200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
11	chr2:73869000-73870200	Flanking Active TSS	Fetal Adrenal Gland	Adrenal Gland
12	chr2:73869000-73870400	Flanking Active TSS	HepG2	liver
13	chr2:73869400-73870200	Enhancers	Primary hematopoietic stem cells short term culture	blood
14	chr2:73869600-73870200	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
15	chr2:73869600-73870200	Enhancers	Fetal Kidney	kidney
16	chr2:73869600-73872000	Enhancers	Lung	lung
17	chr2:73869800-73870200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
18	chr2:73869800-73870200	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
19	chr2:73869800-73870200	Enhancers	Sigmoid Colon	Sigmoid Colon
20	chr2:73869800-73870200	Enhancers	A549	lung
21	chr2:73869800-73870400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
22	chr2:73869800-73870400	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
23	chr2:73870000-73870200	Enhancers	Brain Anterior Caudate	brain
24	chr2:73870000-73870200	Enhancers	Pancreas	Pancrea
25	chr2:73870000-73871000	Weak transcription	Placenta	Placenta
26	chr2:73870000-73872200	Weak transcription	Left Ventricle	heart
27	chr2:73870200-73871200	Enhancers	Liver	Liver
28	chr2:73870200-73871200	Weak transcription	Sigmoid Colon	Sigmoid Colon
29	chr2:73870200-73871600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
30	chr2:73870200-73872200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
31	chr2:73870200-73874600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
32	chr2:73870400-73871800	Enhancers	HepG2	liver
33	chr2:73870600-73873800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
34	chr2:73871000-73871200	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
35	chr2:73871000-73871200	Enhancers	Spleen	Spleen
36	chr2:73871000-73871400	Bivalent Enhancer	H1 Derived Mesenchymal Stem Cells	ES cell derived
37	chr2:73871000-73871400	Enhancers	Placenta	Placenta
38	chr2:73871000-73872200	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
39	chr2:73871200-73871400	Enhancers	Sigmoid Colon	Sigmoid Colon
40	chr2:73871200-73871800	Weak transcription	Spleen	Spleen
41	chr2:73871200-73878800	Weak transcription	Liver	Liver
42	chr2:73871800-73872000	Enhancers	Primary hematopoietic stem cells short term culture	blood
43	chr2:73871800-73872000	Bivalent Enhancer	HepG2	liver
44	chr2:73874600-73876000	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
45	chr2:73875000-73875200	Bivalent Enhancer	H1 Derived Mesenchymal Stem Cells	ES cell derived
46	chr2:73876000-73880800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
47	chr2:73876200-73876400	Enhancers	Fetal Lung	lung
48	chr2:73876400-73877800	Weak transcription	Fetal Lung	lung
49	chr2:73877800-73878600	Enhancers	Fetal Lung	lung
50	chr2:73878200-73878800	Enhancers	Monocytes-CD14+_RO01746	blood

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