Variant report

Variant	esv2759108
Chromosome Location	chr2:188380042-188503185
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2564)
CpG islands
(count:551)
Chromatin interactive
region (count:92)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2564 , 50 per page) page: 1 2 3 4 5 6 7 ... 52

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:188441711-188441904	K562	blood:	n/a	n/a
2	ARID3A	chr2:188411457-188411585	K562	blood:	n/a	n/a
3	ARID3A	chr2:188394446-188395361	HepG2	liver:	n/a	n/a
4	ARID3A	chr2:188445260-188446786	K562	blood:	n/a	n/a
5	ARID3A	chr2:188417779-188418437	HepG2	liver:	n/a	n/a
6	ARID3A	chr2:188411998-188413154	K562	blood:	n/a	n/a
7	ARID3A	chr2:188414115-188414413	HepG2	liver:	n/a	n/a
8	ARID3A	chr2:188391976-188392625	HepG2	liver:	n/a	n/a
9	ARID3A	chr2:188410134-188410334	HepG2	liver:	n/a	n/a
10	ARID3A	chr2:188414692-188415523	HepG2	liver:	n/a	n/a
11	ARID3A	chr2:188412186-188412528	HepG2	liver:	n/a	n/a
12	ARID3A	chr2:188382504-188382798	HepG2	liver:	n/a	n/a
13	ARID3A	chr2:188459686-188459815	K562	blood:	n/a	n/a
14	ARID3A	chr2:188417188-188419388	K562	blood:	n/a	n/a
15	ARID3A	chr2:188416243-188416679	K562	blood:	n/a	n/a
16	ARID3A	chr2:188439872-188439983	K562	blood:	n/a	n/a
17	ARID3A	chr2:188405710-188407124	HepG2	liver:	n/a	n/a
18	ARID3A	chr2:188445189-188446578	HepG2	liver:	n/a	n/a
19	ATF1	chr2:188451755-188452052	K562	blood:	n/a	n/a
20	ATF1	chr2:188412101-188412457	K562	blood:	n/a	n/a
21	ATF1	chr2:188381359-188381631	K562	blood:	n/a	n/a
22	ATF1	chr2:188461274-188461426	K562	blood:	n/a	n/a
23	ATF1	chr2:188417828-188418218	K562	blood:	n/a	n/a
24	ATF3	chr2:188417772-188418260	K562	blood:	n/a	n/a
25	ATF3	chr2:188445228-188445831	K562	blood:	n/a	n/a
26	ATF3	chr2:188412053-188412480	K562	blood:	n/a	n/a
27	ATF3	chr2:188412011-188412662	HCT-116	colon:	n/a	n/a
28	ATF3	chr2:188445322-188445922	A549	lung:	n/a	n/a
29	ATF3	chr2:188412092-188412532	A549	lung:	n/a	n/a
30	ATF3	chr2:188406218-188406907	A549	lung:	n/a	n/a
31	ATF3	chr2:188412150-188412417	K562	blood:	n/a	n/a
32	ATF3	chr2:188394594-188395445	A549	lung:	n/a	n/a
33	ATF3	chr2:188406176-188407188	A549	lung:	n/a	n/a
34	ATF3	chr2:188404393-188405200	HCT-116	colon:	n/a	chr2:188404612-188404623 chr2:188404614-188404622
35	ATF3	chr2:188412043-188412645	HCT-116	colon:	n/a	n/a
36	BACH1	chr2:188417841-188418170	K562	blood:	n/a	n/a
37	BACH1	chr2:188395959-188396172	K562	blood:	n/a	n/a
38	BACH1	chr2:188412142-188412526	K562	blood:	n/a	n/a
39	BACH1	chr2:188411517-188411587	K562	blood:	n/a	n/a
40	BACH1	chr2:188407802-188407916	K562	blood:	n/a	n/a
41	BACH1	chr2:188445366-188445738	K562	blood:	n/a	n/a
42	BATF	chr2:188417919-188418121	GM12878	blood:	n/a	chr2:188418061-188418071 chr2:188418045-188418056 chr2:188418034-188418043 chr2:188418060-188418071
43	BATF	chr2:188417889-188418168	GM12878	blood:	n/a	chr2:188418061-188418071 chr2:188418045-188418056 chr2:188418034-188418043 chr2:188418060-188418071
44	BCL3	chr2:188411972-188412666	A549	lung:	n/a	n/a
45	BCL3	chr2:188394493-188395370	A549	lung:	n/a	n/a
46	BCL3	chr2:188406093-188406881	A549	lung:	n/a	n/a
47	BCL3	chr2:188394124-188395257	A549	lung:	n/a	n/a
48	BCL3	chr2:188417712-188418398	A549	lung:	n/a	n/a
49	BCL3	chr2:188405887-188407122	A549	lung:	n/a	n/a
50	BCL3	chr2:188409053-188409807	A549	lung:	n/a	chr2:188409532-188409539

(count:551 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:188391145-188391195	GM06990	blood:	n/a
2	chr2:188483530-188483580	GM12891	blood:	n/a
3	chr2:188391145-188391195	GM06990	blood:	n/a
4	chr2:188483530-188483580	GM12891	blood:	n/a
5	chr2:188483530-188483580	AG04450	lung:	fetal
6	chr2:188406934-188406984	U87	brain:	n/a
7	chr2:188420266-188420316	K562	blood:	n/a
8	chr2:188483530-188483580	HEK293	kidney:	embryo
9	chr2:188419830-188419880	H1-hESC	embryonic stem cell:	embryo
10	chr2:188483530-188483580	HepG2	liver:	n/a
11	chr2:188419830-188419880	MCF10A-Er-Src	breast:	n/a
12	chr2:188420266-188420316	GM12892	blood:	n/a
13	chr2:188420266-188420316	HRCEpiC	kidney:	n/a
14	chr2:188419830-188419880	HEEpiC	esophagus:	n/a
15	chr2:188483530-188483580	LNCaP	prostate:	n/a
16	chr2:188481707-188481757	HCF	heart:	n/a
17	chr2:188420266-188420316	U87	brain:	n/a
18	chr2:188419830-188419880	AG09319	gingival:	n/a
19	chr2:188483530-188483580	GM06990	blood:	n/a
20	chr2:188420266-188420316	RPTEC	kidney:	n/a
21	chr2:188406934-188406984	GM19239	blood:	n/a
22	chr2:188419830-188419880	HCF	heart:	n/a
23	chr2:188391145-188391195	IMR90	lung:	fetal
24	chr2:188481707-188481757	ECC-1	luminal epithelium:	n/a
25	chr2:188419568-188419618	BE2_C	brain:	n/a
26	chr2:188420266-188420316	GM12878	blood:	n/a
27	chr2:188481707-188481757	HEEpiC	esophagus:	n/a
28	chr2:188391145-188391195	NHDF-neo	bronchial:	n/a
29	chr2:188481707-188481757	BJ	skin:	n/a
30	chr2:188483530-188483580	K562	blood:	n/a
31	chr2:188406934-188406984	NB4	blood:	n/a
32	chr2:188419568-188419618	GM12892	blood:	n/a
33	chr2:188419830-188419880	AG10803	skin:	n/a
34	chr2:188419830-188419880	HRPEpiC	eye:	n/a
35	chr2:188419087-188419137	PFSK-1	brain:	n/a
36	chr2:188481707-188481757	K562	blood:	n/a
37	chr2:188419830-188419880	HEK293	kidney:	embryo
38	chr2:188419087-188419137	NHDF-neo	bronchial:	n/a
39	chr2:188481707-188481757	Jurkat	blood:	n/a
40	chr2:188419830-188419880	SAEC	small airway:	n/a
41	chr2:188483530-188483580	Hela-S3	cervix:	n/a
42	chr2:188419087-188419137	Caco-2	colon:	n/a
43	chr2:188406934-188406984	T-47D	breast:	n/a
44	chr2:188419087-188419137	SAEC	small airway:	n/a
45	chr2:188481707-188481757	ovcar-3	ovarian:	n/a
46	chr2:188481707-188481757	HCT-116	colon:	n/a
47	chr2:188481707-188481757	HRPEpiC	eye:	n/a
48	chr2:188419830-188419880	HMEC	breast:	n/a
49	chr2:188483530-188483580	AG04449	skin:	fetal
50	chr2:188419830-188419880	HPAEpiC	pulmonary alveolar:	n/a

(count:92 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr2:188449920..188452608-chr2:188452638..188454975,2	K562	blood:
2	chr16:73088044..73089636-chr2:188441847..188444162,2	MCF-7	breast:
3	chr2:188389696..188391580-chr2:188402374..188405162,2	K562	blood:
4	chr2:188445350..188448050-chr2:188450278..188452976,4	K562	blood:
5	chr2:188440946..188443688-chr2:188443875..188445768,2	MCF-7	breast:
6	chr2:188350155..188352503-chr2:188415198..188418799,3	K562	blood:
7	chr2:188395046..188397968-chr2:188414786..188417959,4	K562	blood:
8	chr2:188473165..188475172-chr2:188477640..188480014,2	K562	blood:
9	chr2:188393262..188398014-chr2:188414587..188419751,6	K562	blood:
10	chr2:188480199..188482146-chr2:188486058..188487606,2	K562	blood:
11	chr1:146713788..146714307-chr2:188445941..188446637,2	MCF-7	breast:
12	chr2:188404419..188406273-chr2:188410816..188412480,2	MCF-7	breast:
13	chr2:188398970..188401688-chr2:188404214..188406089,3	K562	blood:
14	chr2:188395046..188397968-chr2:188414786..188417959,4	K562	blood:
15	chr2:188445112..188445612-chr2:223767773..223768610,2	K562	blood:
16	chr2:188433750..188436567-chr2:188440064..188442739,2	K562	blood:
17	chr2:188440243..188443082-chr2:188444632..188448024,3	K562	blood:
18	chr2:188480199..188482146-chr2:188486058..188487606,2	K562	blood:
19	chr2:188460269..188463083-chr2:188643990..188646491,2	K562	blood:
20	chr2:188445350..188448050-chr2:188450278..188452976,4	K562	blood:
21	chr2:188362271..188363016-chr2:188446864..188447543,2	MCF-7	breast:
22	chr2:188363950..188366399-chr2:188445083..188446553,13	MCF-7	breast:
23	chr2:188395123..188398204-chr2:188399307..188403080,4	K562	blood:
24	chr2:188349831..188352709-chr2:188404428..188405999,2	K562	blood:
25	chr2:188478443..188481336-chr2:188482033..188484662,2	K562	blood:
26	chr2:188467603..188470192-chr2:188473529..188476139,3	K562	blood:
27	chr2:188408868..188410387-chr2:188412786..188414991,2	MCF-7	breast:
28	chr2:188364663..188366800-chr2:188416557..188418283,2	K562	blood:
29	chr2:188363929..188365341-chr2:188444758..188446502,16	K562	blood:
30	chr2:188390916..188392593-chr2:188395484..188396999,2	K562	blood:
31	chr2:263068..264963-chr2:188441341..188443685,2	MCF-7	breast:
32	chr2:188392650..188395033-chr2:188412614..188414418,2	K562	blood:
33	chr2:188440946..188443688-chr2:188443875..188445768,2	MCF-7	breast:
34	chr2:188446227..188446782-chr2:189376811..189377413,2	K562	blood:
35	chr2:188415101..188417280-chr2:188445536..188447377,2	K562	blood:
36	chr2:188398970..188401688-chr2:188404214..188406089,3	K562	blood:
37	chr2:188478254..188481614-chr2:188483978..188486883,3	K562	blood:
38	chr2:188390916..188392593-chr2:188395484..188396999,2	K562	blood:
39	chr2:188366744..188369184-chr2:188446137..188447850,2	K562	blood:
40	chr2:188415101..188417280-chr2:188445536..188447377,2	K562	blood:
41	chr2:188411707..188414780-chr2:188445119..188447288,3	K562	blood:
42	chr2:188362272..188363211-chr2:188445966..188446643,3	MCF-7	breast:
43	chr2:188480221..188482587-chr2:188496790..188498507,2	K562	blood:
44	chr2:188473583..188475657-chr2:188480041..188481763,2	K562	blood:
45	chr2:187749024..187750695-chr2:188416544..188418279,2	K562	blood:
46	chr2:188410825..188412949-chr2:190475105..190477931,2	K562	blood:
47	chr2:188408868..188410387-chr2:188412786..188414991,2	MCF-7	breast:
48	chr2:188382405..188385031-chr2:188403850..188405817,2	K562	blood:
49	chr2:188387495..188389336-chr2:188392022..188394869,2	MCF-7	breast:
50	chr2:188478254..188481614-chr2:188483978..188486883,3	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FAM171B-1	chr2:188419304-188419390	ENSG00000224063.1
2	lnc-FAM171B-1	chr2:188419003-188419120	ENSG00000224063.1
3	lnc-FAM171B-1	chr2:188418876-188418918	ENSG00000224063.1

No data

Variant related genes	Relation type
TFPI	TF binding region
ENSG00000224063	TF binding region
TFPI	CpG island
ENSG00000224063	CpG island
ENSG00000035115	chromatin interactions
ENSG00000143727	chromatin interactions
ENSG00000131778	chromatin interactions
ENSG00000224063	chromatin interactions
ENSG00000003436	chromatin interactions

Extended variants
information (count: 3648 )
Associated
traits (count: 50 )

Variant overlapped rSNPs/rCNVs (count:3648 , 50 per page) page: 1 2 3 4 5 6 7 ... 73

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs536661867	chr2:188380092-188380093	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs180697029	chr2:188380110-188380111	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs548564546	chr2:188380163-188380164	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs185134781	chr2:188380214-188380215	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs565479887	chr2:188380229-188380230	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs539159093	chr2:188380241-188380242	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs113506049	chr2:188380243-188380244	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs369729884	chr2:188380278-188380279	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs149421357	chr2:188380287-188380288	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs34442590	chr2:188380321-188380322	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs532339576	chr2:188380337-188380338	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs538371723	chr2:188380348-188380349	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs138459634	chr2:188380379-188380380	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs571772085	chr2:188380395-188380396	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs144041138	chr2:188380442-188380443	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs560674547	chr2:188380443-188380444	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs191867142	chr2:188380461-188380462	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs112887396	chr2:188380479-188380480	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs565502940	chr2:188380487-188380488	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs2080345	chr2:188380523-188380524	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs118137565	chr2:188380536-188380537	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs536480796	chr2:188380541-188380542	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs147375549	chr2:188380581-188380582	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs530172300	chr2:188380613-188380614	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs114237320	chr2:188380646-188380647	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs187354678	chr2:188380649-188380650	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs538177801	chr2:188380656-188380657	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs191800079	chr2:188380668-188380669	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs571488453	chr2:188380683-188380684	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs183628109	chr2:188380689-188380690	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs553507693	chr2:188380742-188380743	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs555718309	chr2:188380747-188380748	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs571810872	chr2:188380767-188380768	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs186995758	chr2:188380889-188380890	Weak transcription ZNF genes & repeats Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs190286391	chr2:188380950-188380951	Weak transcription ZNF genes & repeats Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs575931772	chr2:188381034-188381035	Weak transcription ZNF genes & repeats Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs182149618	chr2:188381047-188381048	Weak transcription ZNF genes & repeats Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs543378152	chr2:188381055-188381056	Weak transcription ZNF genes & repeats Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs186887418	chr2:188381245-188381246	Weak transcription ZNF genes & repeats Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs577573687	chr2:188381253-188381254	Weak transcription ZNF genes & repeats Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs573960856	chr2:188381290-188381291	Weak transcription ZNF genes & repeats Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs192445394	chr2:188381356-188381357	Weak transcription ZNF genes & repeats Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs185638754	chr2:188381362-188381363	Weak transcription ZNF genes & repeats Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs537132435	chr2:188381363-188381364	Weak transcription ZNF genes & repeats Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs62172421	chr2:188381367-188381368	Weak transcription ZNF genes & repeats Genic enhancers Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs72906213	chr2:188381374-188381375	Weak transcription ZNF genes & repeats Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs375629398	chr2:188381377-188381378	Weak transcription ZNF genes & repeats Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs10205380	chr2:188381402-188381403	ZNF genes & repeats Weak transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs77176227	chr2:188381434-188381435	ZNF genes & repeats Weak transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs73050518	chr2:188381437-188381438	ZNF genes & repeats Weak transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:50)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	21979893	CNVD
Ependymoma	16718352	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Melanoma	18172304	CNVD
Cancer	16751803	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Testicular germ cell tumor	18059402	CNVD
Breast cancer	16272173	CNVD
Ewing''s sarcoma	17952124	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Autism	16446308	CNVD
Autism	19401682	CNVD
Colorectal cancer	16272173	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Lung cancer	18438408	CNVD
Glioblastoma	21080181	CNVD
Prostate cancer	18632612	CNVD
Acute myeloid leukemia	20729466	CNVD
small cell lung cancer	20016488	CNVD
Facial dysmorphism	20548289	CNVD
Mental retardation	20548289	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Breast cancer	21364760	CNVD
Myelofibrosis	22110671	CNVD
Hirschsprung''s Disease	21712996	CNVD
Cancer	21183584	CNVD
Sudden cardiac death	19188705	CNVD
Autism	19329560	CNVD
Urothelial carcinoma	21177765	CNVD
Intellectual disability	22102821	CNVD
Tetralogy of Fallot	22912587	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:1821 , 50 per page) page: 1 2 3 4 5 6 7 ... 37

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:188360600-188391600	Weak transcription	Psoas Muscle	Psoas
2	chr2:188367200-188383800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
3	chr2:188367600-188381600	Weak transcription	Muscle Satellite Cultured Cells	--
4	chr2:188368400-188383800	Weak transcription	Osteobl	bone
5	chr2:188370000-188389800	Weak transcription	NHDF-Ad	bronchial
6	chr2:188370400-188390000	Weak transcription	Hela-S3	cervix
7	chr2:188374000-188383800	Weak transcription	Liver	Liver
8	chr2:188374400-188384000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
9	chr2:188375000-188384000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
10	chr2:188375200-188400000	Weak transcription	Duodenum Mucosa	Duodenum
11	chr2:188376000-188380400	Weak transcription	Cortex derived primary cultured neurospheres	brain
12	chr2:188376000-188383800	Weak transcription	Placenta Amnion	Placenta Amnion
13	chr2:188376000-188384000	Weak transcription	HUVEC	blood vessel
14	chr2:188376000-188384200	Weak transcription	Left Ventricle	heart
15	chr2:188376000-188385000	Weak transcription	Gastric	stomach
16	chr2:188376400-188383400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
17	chr2:188376400-188383400	Weak transcription	HSMMtube	muscle
18	chr2:188376600-188381400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
19	chr2:188376600-188381400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
20	chr2:188376600-188383400	Weak transcription	HSMM	muscle
21	chr2:188376600-188383800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
22	chr2:188376600-188384000	Weak transcription	Lung	lung
23	chr2:188376800-188381600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
24	chr2:188377000-188384000	Weak transcription	Placenta	Placenta
25	chr2:188377000-188384800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
26	chr2:188378600-188387400	Genic enhancers	HepG2	liver
27	chr2:188378800-188380800	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
28	chr2:188379400-188384000	Weak transcription	NHLF	lung
29	chr2:188379800-188380200	Weak transcription	Fetal Intestine Small	intestine
30	chr2:188379800-188380800	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
31	chr2:188380200-188380800	ZNF genes & repeats	K562	blood
32	chr2:188380400-188380800	ZNF genes & repeats	Cortex derived primary cultured neurospheres	brain
33	chr2:188380800-188381600	Enhancers	K562	blood
34	chr2:188380800-188383800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
35	chr2:188380800-188385400	ZNF genes & repeats	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
36	chr2:188381400-188381800	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
37	chr2:188381400-188381800	ZNF genes & repeats	IMR90 fetal lung fibroblasts Cell Line	lung
38	chr2:188381400-188381800	ZNF genes & repeats	Fetal Intestine Small	intestine
39	chr2:188381600-188381800	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
40	chr2:188381600-188381800	ZNF genes & repeats	Aorta	Aorta
41	chr2:188381600-188382000	Flanking Active TSS	K562	blood
42	chr2:188381600-188388200	Strong transcription	Muscle Satellite Cultured Cells	--
43	chr2:188381800-188382200	Weak transcription	A549	lung
44	chr2:188381800-188384000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
45	chr2:188381800-188385000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
46	chr2:188381800-188406000	Weak transcription	Small Intestine	intestine
47	chr2:188381800-188406600	Weak transcription	Aorta	Aorta
48	chr2:188382000-188382600	Enhancers	K562	blood
49	chr2:188382000-188384200	Weak transcription	Esophagus	oesophagus
50	chr2:188382400-188383000	Weak transcription	A549	lung

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