Variant report

Variant	esv3344704
Chromosome Location	chr2:37192448-37195146
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:659)
CpG islands
(count:488)
Chromatin interactive
region (count:18)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:659 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:37194557-37195345	HepG2	liver:	n/a	n/a
2	ARID3A	chr2:37193591-37194171	HepG2	liver:	n/a	n/a
3	ARID3A	chr2:37194875-37195389	K562	blood:	n/a	n/a
4	ARID3A	chr2:37192499-37192734	K562	blood:	n/a	n/a
5	ATF1	chr2:37193621-37194184	K562	blood:	n/a	n/a
6	ATF2	chr2:37193513-37194453	GM12878	blood:	n/a	n/a
7	ATF2	chr2:37193657-37194244	GM12878	blood:	n/a	n/a
8	ATF3	chr2:37193618-37193918	K562	blood:	n/a	chr2:37193733-37193742
9	ATF3	chr2:37193339-37193621	HepG2	liver:	n/a	n/a
10	BACH1	chr2:37193057-37193778	H1-hESC	embryonic stem cell:	n/a	n/a
11	BACH1	chr2:37193979-37194421	H1-hESC	embryonic stem cell:	n/a	n/a
12	BCL3	chr2:37193785-37194419	A549	lung:	n/a	chr2:37194170-37194183
13	BCLAF1	chr2:37193440-37194364	GM12878	blood:	n/a	chr2:37193645-37193654 chr2:37194170-37194183 chr2:37193640-37193653 chr2:37193633-37193646 chr2:37193686-37193695
14	BCLAF1	chr2:37193449-37194144	K562	blood:	n/a	chr2:37193645-37193654 chr2:37193640-37193653 chr2:37193633-37193646 chr2:37193686-37193695
15	BCLAF1	chr2:37193508-37194370	K562	blood:	n/a	chr2:37193645-37193654 chr2:37194170-37194183 chr2:37193640-37193653 chr2:37193633-37193646 chr2:37193686-37193695
16	BHLHE40	chr2:37193393-37194433	GM12878	blood:	n/a	chr2:37193635-37193651
17	BHLHE40	chr2:37195124-37195308	K562	blood:	n/a	n/a
18	BHLHE40	chr2:37192887-37193122	GM12878	blood:	n/a	n/a
19	BHLHE40	chr2:37193439-37194400	K562	blood:	n/a	chr2:37193635-37193651
20	BHLHE40	chr2:37194689-37195186	HepG2	liver:	n/a	n/a
21	BHLHE40	chr2:37192822-37193156	K562	blood:	n/a	n/a
22	BHLHE40	chr2:37193589-37194382	HepG2	liver:	n/a	chr2:37193635-37193651
23	BRCA1	chr2:37193601-37193856	Hela-S3	cervix:	n/a	n/a
24	CBX3	chr2:37193501-37194576	K562	blood:	n/a	n/a
25	CBX3	chr2:37194631-37196191	K562	blood:	n/a	n/a
26	CCNT2	chr2:37193342-37194335	K562	blood:	n/a	n/a
27	CEBPB	chr2:37193710-37193766	H1-hESC	embryonic stem cell:	n/a	n/a
28	CEBPB	chr2:37193573-37194192	A549	lung:	n/a	n/a
29	CEBPB	chr2:37193685-37194091	HepG2	liver:	n/a	n/a
30	CEBPB	chr2:37192408-37192722	Hela-S3	cervix:	n/a	chr2:37192570-37192581 chr2:37192570-37192583
31	CEBPB	chr2:37192449-37192702	IMR90	lung:	n/a	chr2:37192570-37192581 chr2:37192570-37192583
32	CEBPB	chr2:37193799-37193897	K562	blood:	n/a	n/a
33	CEBPB	chr2:37192399-37192723	K562	blood:	n/a	chr2:37192570-37192581 chr2:37192570-37192583
34	CEBPB	chr2:37193601-37194223	Hela-S3	cervix:	n/a	n/a
35	CEBPD	chr2:37193429-37193869	HepG2	liver:	n/a	n/a
36	CEBPD	chr2:37193631-37194074	HepG2	liver:	n/a	n/a
37	CHD1	chr2:37194122-37194378	H1-hESC	embryonic stem cell:	n/a	n/a
38	CHD1	chr2:37194086-37194286	GM12878	blood:	n/a	n/a
39	CHD1	chr2:37192535-37192539	GM12878	blood:	n/a	n/a
40	CHD2	chr2:37193531-37194319	K562	blood:	n/a	n/a
41	CHD2	chr2:37193088-37194472	GM12878	blood:	n/a	chr2:37193311-37193321
42	CHD2	chr2:37192766-37194390	Hela-S3	cervix:	n/a	chr2:37193311-37193321
43	CHD2	chr2:37193215-37193285	HepG2	liver:	n/a	n/a
44	CHD2	chr2:37193017-37193421	H1-hESC	embryonic stem cell:	n/a	chr2:37193311-37193321
45	CHD2	chr2:37193079-37193322	K562	blood:	n/a	chr2:37193311-37193321
46	CHD2	chr2:37193532-37194035	HepG2	liver:	n/a	n/a
47	CHD2	chr2:37193641-37194060	H1-hESC	embryonic stem cell:	n/a	n/a
48	CHD2	chr2:37194943-37195295	K562	blood:	n/a	chr2:37195134-37195144
49	CHD2	chr2:37194897-37195202	HepG2	liver:	n/a	chr2:37195134-37195144
50	CREB1	chr2:37193467-37194569	K562	blood:	n/a	n/a

(count:488 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:37192797-37192847	HNPCEpiC	eye:	n/a
2	chr2:37194071-37194121	H1-hESC	embryonic stem cell:	embryo
3	chr2:37194155-37194205	HCPEpiC	choroid plexus:	n/a
4	chr2:37194155-37194205	HNPCEpiC	eye:	n/a
5	chr2:37193060-37193110	AG09319	gingival:	n/a
6	chr2:37193060-37193110	NB4	blood:	n/a
7	chr2:37193690-37193740	U87	brain:	n/a
8	chr2:37193358-37193408	AoSMC	blood vessel:	n/a
9	chr2:37194155-37194205	HRPEpiC	eye:	n/a
10	chr2:37193690-37193740	K562	blood:	n/a
11	chr2:37193358-37193408	AG04450	lung:	fetal
12	chr2:37193060-37193110	HRE	kidney:	n/a
13	chr2:37194155-37194205	NT2-D1	testis:	n/a
14	chr2:37193481-37193531	AG10803	skin:	n/a
15	chr2:37192797-37192847	H1-hESC	embryonic stem cell:	embryo
16	chr2:37193481-37193531	GM06990	blood:	n/a
17	chr2:37194155-37194205	GM12878	blood:	n/a
18	chr2:37192797-37192847	SAEC	small airway:	n/a
19	chr2:37193358-37193408	ECC-1	luminal epithelium:	n/a
20	chr2:37194071-37194121	SK-N-SH_RA	brain:	n/a
21	chr2:37194356-37194406	A549	lung:	n/a
22	chr2:37194071-37194121	AoSMC	blood vessel:	n/a
23	chr2:37192797-37192847	AoSMC	blood vessel:	n/a
24	chr2:37193690-37193740	HMEC	breast:	n/a
25	chr2:37193358-37193408	SK-N-SH	brain:	n/a
26	chr2:37193481-37193531	BJ	skin:	n/a
27	chr2:37192797-37192847	CMK	blood:	n/a
28	chr2:37193690-37193740	AG09309	skin:	n/a
29	chr2:37193358-37193408	HCPEpiC	choroid plexus:	n/a
30	chr2:37193481-37193531	AG04449	skin:	fetal
31	chr2:37193358-37193408	SAEC	small airway:	n/a
32	chr2:37193358-37193408	NB4	blood:	n/a
33	chr2:37193481-37193531	PANC-1	pancreas:	n/a
34	chr2:37193481-37193531	Jurkat	blood:	n/a
35	chr2:37193358-37193408	Caco-2	colon:	n/a
36	chr2:37193358-37193408	A549	lung:	n/a
37	chr2:37194155-37194205	HAEpiC	amniotic membrane:	n/a
38	chr2:37193481-37193531	NHDF-neo	bronchial:	n/a
39	chr2:37192797-37192847	SK-N-SH_RA	brain:	n/a
40	chr2:37194356-37194406	HUVEC	blood vessel:	n/a
41	chr2:37193060-37193110	PANC-1	pancreas:	n/a
42	chr2:37193060-37193110	AG04450	lung:	fetal
43	chr2:37194155-37194205	AoSMC	blood vessel:	n/a
44	chr2:37194155-37194205	SK-N-SH_RA	brain:	n/a
45	chr2:37193358-37193408	GM19239	blood:	n/a
46	chr2:37193060-37193110	HIPEpiC	eye:	n/a
47	chr2:37192797-37192847	GM12878	blood:	n/a
48	chr2:37193358-37193408	GM06990	blood:	n/a
49	chr2:37193358-37193408	NH-A	brain:	n/a
50	chr2:37194071-37194121	AG09309	skin:	n/a

(count:18 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:37183661..37187179-chr2:37192061..37194972,3	MCF-7	breast:
2	chr2:37193659..37195188-chr2:37231958..37233613,2	MCF-7	breast:
3	chr17:79478375..79479269-chr2:37193649..37194542,2	HCT-116	colon:
4	chr2:37194252..37196693-chr2:37198973..37200836,2	MCF-7	breast:
5	chr2:37194557..37197275-chr2:37197696..37199511,3	K562	blood:
6	chr2:37194247..37196675-chr2:37203224..37205629,3	K562	blood:
7	chr2:37193543..37195604-chr2:37419400..37421969,2	K562	blood:
8	chr2:37193759..37194604-chr6:30294819..30295525,2	Hela-S3	cervix:
9	chr11:67141563..67142093-chr2:37193174..37193824,2	Hela-S3	cervix:
10	chr2:37186145..37190956-chr2:37191183..37194668,5	K562	blood:
11	chr2:37114816..37116390-chr2:37191550..37193356,2	MCF-7	breast:
12	chr2:37192443..37195662-chr2:37309226..37313144,4	K562	blood:
13	chr2:37194014..37195839-chr2:37202260..37204776,2	MCF-7	breast:
14	chr2:37170595..37172882-chr2:37190992..37193264,2	K562	blood:
15	chr16:20752849..20753363-chr2:37192986..37193858,2	HCT-116	colon:
16	chr2:37194465..37196285-chr2:37212369..37214230,2	K562	blood:
17	chr2:37191677..37193362-chr2:37233119..37235779,2	K562	blood:
18	chr2:37181946..37184586-chr2:37193992..37195533,2	K562	blood:

No data

Variant related genes	Relation type
STRN	TF binding region
STRN	CpG island
ENSG00000066654	chromatin interactions
ENSG00000231074	chromatin interactions
ENSG00000175505	chromatin interactions
ENSG00000184009	chromatin interactions
ENSG00000252518	chromatin interactions
ENSG00000152133	chromatin interactions
ENSG00000008869	chromatin interactions
ENSG00000233159	chromatin interactions
ENSG00000204599	chromatin interactions

Extended variants
information (count: 92 )
Associated
traits (count: 65 )

Variant overlapped rSNPs/rCNVs (count:92 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs543807940	chr2:37192471-37192472	Active TSS Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
2	rs3770774	chr2:37192495-37192496	Active TSS Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
3	rs547730845	chr2:37192505-37192506	Active TSS Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs548027187	chr2:37192519-37192520	Active TSS Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs151277576	chr2:37192533-37192534	Active TSS Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs140521043	chr2:37192541-37192542	Active TSS Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs190605242	chr2:37192550-37192551	Active TSS Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs3770773	chr2:37192561-37192562	Active TSS Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs571187408	chr2:37192601-37192602	Active TSS Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs3770772	chr2:37192607-37192608	Active TSS Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs556585663	chr2:37192670-37192671	Active TSS Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs3770771	chr2:37192768-37192769	Active TSS Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs535919540	chr2:37192843-37192844	Active TSS Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs13416935	chr2:37192860-37192861	Active TSS Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs3770770	chr2:37192866-37192867	Active TSS Flanking Active TSS	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
16	rs572957666	chr2:37192930-37192931	Active TSS Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs540077156	chr2:37192952-37192953	Active TSS Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs558383859	chr2:37192967-37192968	Active TSS Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs576736572	chr2:37192969-37192970	Active TSS Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs544141709	chr2:37192981-37192982	Active TSS Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs373629573	chr2:37193028-37193029	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
22	rs145208570	chr2:37193051-37193052	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
23	rs559922136	chr2:37193054-37193055	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
24	rs541894653	chr2:37193061-37193062	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
25	rs3770769	chr2:37193075-37193076	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
26	rs146907807	chr2:37193083-37193084	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
27	rs552811333	chr2:37193086-37193087	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
28	rs548623849	chr2:37193137-37193138	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
29	rs571093230	chr2:37193156-37193157	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
30	rs532037872	chr2:37193198-37193199	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
31	rs550521181	chr2:37193237-37193238	Active TSS Transcr. at gene 5' and 3' Weak transcription Bivalent/Poised TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
32	rs568425295	chr2:37193257-37193258	Active TSS Transcr. at gene 5' and 3' Weak transcription Bivalent/Poised TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
33	rs367721265	chr2:37193403-37193404	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Weak transcription Bivalent/Poised TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
34	rs371321067	chr2:37193424-37193425	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Weak transcription Bivalent/Poised TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
35	rs376191070	chr2:37193425-37193426	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Weak transcription Bivalent/Poised TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
36	rs535495726	chr2:37193627-37193628	Active TSS Weak transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
37	rs554211047	chr2:37193637-37193638	Active TSS Weak transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
38	rs569327763	chr2:37193648-37193649	Active TSS Weak transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
39	rs566042948	chr2:37193649-37193650	Active TSS Weak transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
40	rs533948442	chr2:37193676-37193677	Active TSS Weak transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
41	rs566785343	chr2:37193707-37193708	Active TSS Weak transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
42	rs558321934	chr2:37193793-37193794	Active TSS Weak transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
43	rs534051022	chr2:37193794-37193795	Active TSS Weak transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
44	rs182892849	chr2:37193925-37193926	Active TSS Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
45	rs537726942	chr2:37193961-37193962	Active TSS Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
46	rs139316650	chr2:37193962-37193963	Active TSS Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
47	rs574341705	chr2:37193988-37193989	Active TSS Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
48	rs143213742	chr2:37193998-37193999	Active TSS Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
49	rs560149811	chr2:37194001-37194002	Active TSS Bivalent/Poised TSS Flanking Active TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
50	rs6736165	chr2:37194037-37194038	Active TSS Bivalent/Poised TSS Flanking Active TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:65)

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
Breast cancer	21364760	CNVD
Wilms tumour	21544195	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
T-cell lymphomas	22341440	CNVD
Breast cancer	22522925	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD

Chromatin state (count:435 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:37179200-37192800	Weak transcription	Lung	lung
2	chr2:37186600-37192600	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
3	chr2:37187400-37192600	Weak transcription	Fetal Muscle Trunk	muscle
4	chr2:37189200-37192600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
5	chr2:37190200-37192800	Enhancers	Sigmoid Colon	Sigmoid Colon
6	chr2:37191000-37192600	Enhancers	Primary B cells from peripheral blood	blood
7	chr2:37191000-37192600	Enhancers	Small Intestine	intestine
8	chr2:37191000-37192800	Enhancers	Spleen	Spleen
9	chr2:37191200-37192800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
10	chr2:37191200-37192800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
11	chr2:37191400-37192800	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
12	chr2:37191600-37192600	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
13	chr2:37191600-37192600	Enhancers	Primary T cells fromperipheralblood	blood
14	chr2:37191600-37192600	Flanking Active TSS	Rectal Mucosa Donor 29	rectum
15	chr2:37191600-37192800	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
16	chr2:37191600-37192800	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
17	chr2:37191600-37193200	Flanking Active TSS	Dnd41	blood
18	chr2:37191600-37194600	Active TSS	HUES6 Cell Line	embryonic stem cell
19	chr2:37191600-37194600	Active TSS	NHLF	lung
20	chr2:37191800-37192600	Enhancers	Primary monocytes fromperipheralblood	blood
21	chr2:37191800-37192600	Enhancers	Primary B cells from cord blood	blood
22	chr2:37191800-37192600	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
23	chr2:37191800-37192600	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
24	chr2:37191800-37192600	Flanking Active TSS	Muscle Satellite Cultured Cells	--
25	chr2:37191800-37192600	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
26	chr2:37191800-37192600	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
27	chr2:37191800-37192600	Enhancers	Brain Substantia Nigra	brain
28	chr2:37191800-37192600	Flanking Active TSS	A549	lung
29	chr2:37191800-37192800	Flanking Active TSS	Primary T helper 17 cells PMA-I stimulated	--
30	chr2:37191800-37192800	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
31	chr2:37191800-37193000	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
32	chr2:37191800-37193000	Active TSS	Right Atrium	heart
33	chr2:37191800-37193200	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
34	chr2:37191800-37193200	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
35	chr2:37191800-37193200	Flanking Active TSS	Rectal Mucosa Donor 31	rectum
36	chr2:37191800-37194000	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
37	chr2:37191800-37194400	Active TSS	Esophagus	oesophagus
38	chr2:37191800-37194600	Active TSS	H9 Cell Line	embryonic stem cell
39	chr2:37191800-37194600	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
40	chr2:37191800-37194600	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
41	chr2:37191800-37194600	Active TSS	Left Ventricle	heart
42	chr2:37191800-37195000	Active TSS	NHDF-Ad	bronchial
43	chr2:37192000-37192600	Enhancers	Liver	Liver
44	chr2:37192000-37192600	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
45	chr2:37192000-37192600	Flanking Active TSS	Stomach Smooth Muscle	stomach
46	chr2:37192000-37192800	Flanking Active TSS	Breast Myoepithelial Primary Cells	Breast
47	chr2:37192000-37192800	Flanking Active TSS	Primary T cells from cord blood	blood
48	chr2:37192000-37192800	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
49	chr2:37192000-37192800	Flanking Active TSS	Hela-S3	cervix
50	chr2:37192000-37192800	Flanking Active TSS	HUVEC	blood vessel

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