Variant report

Variant	nsv834468
Chromosome Location	chr2:179351116-179533625
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1245)
CpG islands
(count:1344)
Chromatin interactive
region (count:161)
LncRNA
region (count:10)
Mature miRNA
region (count: 0)
miRNA target
sites (count:3)

(count:1245 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:179362759-179363188	K562	blood:	n/a	n/a
2	ARID3A	chr2:179356423-179356717	K562	blood:	n/a	n/a
3	ARID3A	chr2:179387757-179387925	HepG2	liver:	n/a	n/a
4	ARID3A	chr2:179387494-179388091	K562	blood:	n/a	n/a
5	ATF1	chr2:179362905-179363251	K562	blood:	n/a	n/a
6	ATF1	chr2:179387611-179388555	K562	blood:	n/a	n/a
7	ATF1	chr2:179484133-179484152	K562	blood:	n/a	n/a
8	ATF2	chr2:179393899-179394318	GM12878	blood:	n/a	n/a
9	ATF2	chr2:179387522-179388185	GM12878	blood:	n/a	n/a
10	ATF2	chr2:179387574-179388128	H1-hESC	embryonic stem cell:	n/a	n/a
11	ATF2	chr2:179387575-179388106	H1-hESC	embryonic stem cell:	n/a	n/a
12	ATF2	chr2:179387561-179388154	GM12878	blood:	n/a	n/a
13	ATF2	chr2:179395108-179396236	GM12878	blood:	n/a	n/a
14	ATF2	chr2:179393813-179394341	GM12878	blood:	n/a	n/a
15	ATF2	chr2:179392303-179392821	GM12878	blood:	n/a	n/a
16	ATF2	chr2:179392255-179392901	GM12878	blood:	n/a	n/a
17	ATF2	chr2:179372095-179372565	GM12878	blood:	n/a	n/a
18	ATF2	chr2:179394891-179396186	GM12878	blood:	n/a	n/a
19	ATF3	chr2:179356364-179356608	K562	blood:	n/a	n/a
20	ATF3	chr2:179387592-179388089	K562	blood:	n/a	n/a
21	ATF3	chr2:179387701-179388051	K562	blood:	n/a	n/a
22	BACH1	chr2:179387720-179388047	H1-hESC	embryonic stem cell:	n/a	n/a
23	BACH1	chr2:179393880-179393974	K562	blood:	n/a	n/a
24	BATF	chr2:179379405-179379695	GM12878	blood:	n/a	chr2:179379500-179379511
25	BATF	chr2:179395174-179395863	GM12878	blood:	n/a	n/a
26	BATF	chr2:179372203-179372489	GM12878	blood:	n/a	n/a
27	BATF	chr2:179392498-179392872	GM12878	blood:	n/a	n/a
28	BATF	chr2:179355333-179355572	GM12878	blood:	n/a	n/a
29	BATF	chr2:179372200-179372417	GM12878	blood:	n/a	n/a
30	BATF	chr2:179395261-179395830	GM12878	blood:	n/a	n/a
31	BATF	chr2:179392222-179392892	GM12878	blood:	n/a	n/a
32	BCL11A	chr2:179395162-179395911	GM12878	blood:	n/a	n/a
33	BCL11A	chr2:179395225-179395856	GM12878	blood:	n/a	n/a
34	BCL3	chr2:179395262-179395880	GM12878	blood:	n/a	n/a
35	BCL3	chr2:179395365-179395837	GM12878	blood:	n/a	n/a
36	BCLAF1	chr2:179387586-179388239	GM12878	blood:	n/a	n/a
37	BCLAF1	chr2:179387566-179388269	GM12878	blood:	n/a	n/a
38	BCLAF1	chr2:179395028-179396123	GM12878	blood:	n/a	n/a
39	BCLAF1	chr2:179395119-179396036	GM12878	blood:	n/a	n/a
40	BHLHE40	chr2:179393902-179394333	GM12878	blood:	n/a	n/a
41	BHLHE40	chr2:179395075-179396058	GM12878	blood:	n/a	n/a
42	BHLHE40	chr2:179388430-179388672	GM12878	blood:	n/a	n/a
43	BHLHE40	chr2:179387471-179388546	K562	blood:	n/a	n/a
44	BHLHE40	chr2:179356548-179356577	K562	blood:	n/a	n/a
45	BHLHE40	chr2:179387613-179388138	GM12878	blood:	n/a	n/a
46	BRCA1	chr2:179387670-179388018	Hela-S3	cervix:	n/a	n/a
47	CBX3	chr2:179356313-179356817	K562	blood:	n/a	n/a
48	CBX3	chr2:179387374-179388067	K562	blood:	n/a	n/a
49	CBX3	chr2:179387202-179388625	K562	blood:	n/a	n/a
50	CCNT2	chr2:179449741-179449827	K562	blood:	n/a	n/a

(count:1344 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:179391695-179391745	HMEC	breast:	n/a
2	chr2:179396214-179396264	HCF	heart:	n/a
3	chr2:179391695-179391745	HMEC	breast:	n/a
4	chr2:179396214-179396264	HCF	heart:	n/a
5	chr2:179396214-179396264	HMEC	breast:	n/a
6	chr2:179428333-179428383	SK-N-SH	brain:	n/a
7	chr2:179391695-179391745	SK-N-SH	brain:	n/a
8	chr2:179440846-179440896	HMEC	breast:	n/a
9	chr2:179428333-179428383	IMR90	lung:	fetal
10	chr2:179397513-179397563	GM19239	blood:	n/a
11	chr2:179395885-179395935	SK-N-SH_RA	brain:	n/a
12	chr2:179396826-179396876	BE2_C	brain:	n/a
13	chr2:179395935-179395985	HNPCEpiC	eye:	n/a
14	chr2:179395935-179395985	HCT-116	colon:	n/a
15	chr2:179428333-179428383	ECC-1	luminal epithelium:	n/a
16	chr2:179371342-179371392	SK-N-MC	brain:	n/a
17	chr2:179440846-179440896	LNCaP	prostate:	n/a
18	chr2:179428333-179428383	PrEC	prostate:	n/a
19	chr2:179397435-179397485	HEEpiC	esophagus:	n/a
20	chr2:179396214-179396264	K562	blood:	n/a
21	chr2:179397060-179397110	HNPCEpiC	eye:	n/a
22	chr2:179395912-179395962	HRE	kidney:	n/a
23	chr2:179388064-179388114	PFSK-1	brain:	n/a
24	chr2:179397513-179397563	HNPCEpiC	eye:	n/a
25	chr2:179396826-179396876	AG09309	skin:	n/a
26	chr2:179428333-179428383	HAEpiC	amniotic membrane:	n/a
27	chr2:179440846-179440896	HRPEpiC	eye:	n/a
28	chr2:179397483-179397533	HRPEpiC	eye:	n/a
29	chr2:179396688-179396738	Caco-2	colon:	n/a
30	chr2:179396750-179396800	A549	lung:	n/a
31	chr2:179387853-179387903	HUVEC	blood vessel:	n/a
32	chr2:179395885-179395935	AG04450	lung:	fetal
33	chr2:179397060-179397110	NHDF-neo	bronchial:	n/a
34	chr2:179397513-179397563	PFSK-1	brain:	n/a
35	chr2:179397060-179397110	HEK293	kidney:	embryo
36	chr2:179440846-179440896	T-47D	breast:	n/a
37	chr2:179395885-179395935	PrEC	prostate:	n/a
38	chr2:179387853-179387903	HRE	kidney:	n/a
39	chr2:179397483-179397533	NB4	blood:	n/a
40	chr2:179397008-179397058	HMEC	breast:	n/a
41	chr2:179395912-179395962	Hepatocyte	liver:	n/a
42	chr2:179371342-179371392	SK-N-SH_RA	brain:	n/a
43	chr2:179397483-179397533	MCF10A-Er-Src	breast:	n/a
44	chr2:179387853-179387903	HMEC	breast:	n/a
45	chr2:179397483-179397533	GM12891	blood:	n/a
46	chr2:179397483-179397533	HPAEpiC	pulmonary alveolar:	n/a
47	chr2:179397483-179397533	HNPCEpiC	eye:	n/a
48	chr2:179397060-179397110	Caco-2	colon:	n/a
49	chr2:179388064-179388114	LNCaP	prostate:	n/a
50	chr2:179395912-179395962	SKMC	muscle:	n/a

(count:161 , 50 per page) page: 1 2 3 4

No.	Distal block	Cell Line	Cell type
1	chr2:179386627..179389310-chr2:179394176..179396606,2	MCF-7	breast:
2	chr2:179442770..179444803-chr2:179445864..179448821,2	K562	blood:
3	chr2:179359085..179362406-chr2:179364736..179367288,3	MCF-7	breast:
4	chr2:179354662..179357562-chr2:179362398..179365537,4	K562	blood:
5	chr2:179418405..179420692-chr2:179421306..179423003,2	K562	blood:
6	chr2:179315026..179317909-chr2:179421262..179423691,2	K562	blood:
7	chr2:179371835..179375204-chr2:179376533..179381203,4	K562	blood:
8	chr2:179356489..179359180-chr2:179374513..179376046,2	K562	blood:
9	chr2:178934356..178936456-chr2:179417127..179418784,2	K562	blood:
10	chr2:179344389..179346577-chr2:179386170..179387840,3	K562	blood:
11	chr2:179342456..179345399-chr2:179459226..179461256,2	K562	blood:
12	chr2:179375119..179377100-chr2:179387989..179390246,2	K562	blood:
13	chr2:179434791..179437308-chr2:179438130..179440341,2	K562	blood:
14	chr2:179313562..179315842-chr2:179413934..179415577,2	K562	blood:
15	chr2:179532392..179535244-chr2:179536264..179538357,2	K562	blood:
16	chr2:179347333..179349438-chr2:179354619..179356582,3	MCF-7	breast:
17	chr2:179432790..179436322-chr2:179437819..179441282,4	MCF-7	breast:
18	chr2:179411316..179413406-chr2:179423053..179424886,2	K562	blood:
19	chr2:179350604..179352787-chr2:179436385..179438002,2	K562	blood:
20	chr2:179422561..179427533-chr2:179432302..179436598,7	K562	blood:
21	chr2:179315613..179317763-chr2:179416456..179418128,2	K562	blood:
22	chr2:179355382..179358080-chr2:179358228..179361281,3	K562	blood:
23	chr2:179422059..179424305-chr2:179427109..179429987,2	K562	blood:
24	chr2:179368753..179371424-chr2:179372285..179374100,2	MCF-7	breast:
25	chr2:179425306..179427533-chr2:179432261..179435221,2	K562	blood:
26	chr2:179406739..179408388-chr2:179412036..179413753,2	K562	blood:
27	chr2:179315022..179316850-chr2:179386187..179387838,2	MCF-7	breast:
28	chr2:179371911..179375204-chr2:179378551..179381975,3	K562	blood:
29	chr2:179356489..179359180-chr2:179374513..179376046,2	K562	blood:
30	chr2:179478844..179481420-chr2:179485516..179488514,3	K562	blood:
31	chr2:179368753..179371424-chr2:179372285..179374100,2	MCF-7	breast:
32	chr2:179341858..179343792-chr2:179500377..179502025,2	K562	blood:
33	chr2:179395770..179398427-chr2:179417927..179420746,2	K562	blood:
34	chr2:179373268..179374889-chr2:179377479..179379778,2	MCF-7	breast:
35	chr2:179395497..179400266-chr2:179412543..179417721,4	K562	blood:
36	chr2:179349410..179352916-chr2:179365424..179367731,3	K562	blood:
37	chr2:179414832..179418077-chr2:179421948..179424136,3	K562	blood:
38	chr2:179349895..179352198-chr2:179353151..179354853,2	K562	blood:
39	chr2:179440588..179442582-chr2:179446121..179449484,3	K562	blood:
40	chr2:179413558..179416652-chr2:179422354..179425366,4	K562	blood:
41	chr2:179361307..179367061-chr2:179369825..179374602,5	K562	blood:
42	chr2:179434791..179437308-chr2:179438130..179440341,2	K562	blood:
43	chr2:179342985..179345666-chr2:179370869..179373805,2	MCF-7	breast:
44	chr2:179312948..179315940-chr2:179423067..179424603,2	K562	blood:
45	chr2:179377244..179379642-chr2:179381924..179384722,3	K562	blood:
46	chr2:179421259..179423141-chr2:179424971..179426948,2	K562	blood:
47	chr2:179406083..179407672-chr2:179433537..179435073,2	K562	blood:
48	chr2:179462491..179465326-chr2:179473182..179475653,2	K562	blood:
49	chr2:179410068..179413369-chr2:179416784..179418965,3	K562	blood:
50	chr2:179343119..179348103-chr2:179349634..179353347,6	MCF-7	breast:

(count:10 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PLEKHA3-1	chr2:179465285-179465394	ENSG00000237298.4
2	lnc-PLEKHA3-2	chr2:179510454-179510650	ENSG00000234483.1
3	lnc-PLEKHA3-1	chr2:179388284-179388363	ENSG00000237298.4
4	lnc-PLEKHA3-1	chr2:179509021-179509228	ENSG00000237298.4
5	lnc-PLEKHA3-1	chr2:179391923-179392104	ENSG00000237298.4
6	lnc-PLEKHA3-2	chr2:179501287-179501425	ENSG00000234483.1
7	lnc-PLEKHA3-13	chr2:179481308-179481850	ENSG00000271141.1
8	lnc-PLEKHA3-2	chr2:179509021-179509228	ENSG00000234483.1
9	lnc-PLEKHA3-1	chr2:179388814-179388950	ENSG00000237298.4
10	lnc-PLEKHA3-15	chr2:179509444-179509906	ENSG00000271401.1

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location
1	PLEKHA3	hsa-miR-133a-3p	chr2:179369006-179369026
2	PLEKHA3	hsa-miR-375	chr2:179368836-179368857
3	PLEKHA3	hsa-miR-375	chr2:179369577-179369598

Variant related genes	Relation type
PLEKHA3	TF binding region
ENSG00000270277	TF binding region
TTN	TF binding region
ENSG00000270574	TF binding region
TTN-AS1	TF binding region
ENSG00000271141	TF binding region
ENSG00000270956	TF binding region
ENSG00000271011	TF binding region
ENSG00000271401	TF binding region
PLEKHA3	CpG island
ENSG00000270277	CpG island
TTN	CpG island
ENSG00000270574	CpG island
TTN-AS1	CpG island
ENSG00000271141	CpG island
ENSG00000270956	CpG island
ENSG00000271011	CpG island
ENSG00000271401	CpG island
ENSG00000204311	chromatin interactions
ENSG00000271011	chromatin interactions
ENSG00000180228	chromatin interactions
ENSG00000155657	chromatin interactions
ENSG00000270574	chromatin interactions
ENSG00000116095	chromatin interactions
ENSG00000271141	chromatin interactions
ENSG00000270277	chromatin interactions
ENSG00000079150	chromatin interactions
ENSG00000237298	chromatin interactions
ENSG00000270956	chromatin interactions
ENSG00000271401	chromatin interactions

Extended variants
information (count: 7898 )
Associated
traits (count: 57 )

Variant overlapped rSNPs/rCNVs (count:7898 , 50 per page) page: 1 2 3 4 5 6 7 ... 158

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs535413988	chr2:179351139-179351140	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
2	rs555656934	chr2:179351148-179351149	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
3	rs546921723	chr2:179351169-179351170	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
4	rs572237349	chr2:179351209-179351210	Weak transcription Strong transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
5	rs145560289	chr2:179351321-179351322	Weak transcription Strong transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
6	rs199594076	chr2:179351322-179351323	Weak transcription Strong transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
7	rs80046425	chr2:179351324-179351325	Weak transcription Strong transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
8	rs534820894	chr2:179351360-179351361	Weak transcription Strong transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
9	rs558237609	chr2:179351378-179351379	Weak transcription Strong transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
10	rs62176135	chr2:179351409-179351410	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs12613303	chr2:179351565-179351566	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs563559894	chr2:179351587-179351588	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
13	rs573999135	chr2:179351608-179351609	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
14	rs200811484	chr2:179351610-179351611	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
15	rs62176136	chr2:179351633-179351634	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
16	rs542916325	chr2:179351691-179351692	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
17	rs59180759	chr2:179351746-179351747	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
18	rs377147402	chr2:179351825-179351826	Weak transcription Strong transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
19	rs374910568	chr2:179351828-179351829	Weak transcription Strong transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
20	rs551602959	chr2:179351850-179351851	Weak transcription Strong transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
21	rs369369603	chr2:179351857-179351858	Weak transcription Strong transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
22	rs372855648	chr2:179351996-179351997	Weak transcription Strong transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
23	rs370285374	chr2:179352018-179352019	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
24	rs374323136	chr2:179352074-179352075	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
25	rs374866997	chr2:179352110-179352111	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
26	rs145724082	chr2:179352141-179352142	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
27	rs201487129	chr2:179352148-179352149	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
28	rs199928282	chr2:179352149-179352150	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
29	rs374906553	chr2:179352153-179352154	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
30	rs200669543	chr2:179352175-179352176	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
31	rs532899986	chr2:179352197-179352198	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
32	rs549730269	chr2:179352235-179352236	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
33	rs111308939	chr2:179352239-179352240	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
34	rs535448842	chr2:179352251-179352252	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
35	rs189780416	chr2:179352292-179352293	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
36	rs565983937	chr2:179352305-179352306	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
37	rs73036330	chr2:179352362-179352363	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs558017259	chr2:179352364-179352365	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
39	rs571747126	chr2:179352377-179352378	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
40	rs537575037	chr2:179352379-179352380	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
41	rs375014295	chr2:179352409-179352410	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
42	rs557442186	chr2:179352418-179352419	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
43	rs573908392	chr2:179352432-179352433	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
44	rs7588593	chr2:179352450-179352451	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs553245790	chr2:179352492-179352493	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
46	rs74410041	chr2:179352507-179352508	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
47	rs182955652	chr2:179352513-179352514	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
48	rs370913332	chr2:179352619-179352620	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
49	rs565167008	chr2:179352631-179352632	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
50	rs531033183	chr2:179352698-179352699	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:57)

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
Intellectual disability	22102821	CNVD
Autism	18522746	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
Seminomas	18059402	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
Invasive pancreatic ductal carcinoma	16982739	CNVD
Prostate cancer	18632612	CNVD
Sudden cardiac death	19188705	CNVD
Acute myeloid leukemia	20729466	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
small cell lung cancer	20016488	CNVD
Myelofibrosis	22110671	CNVD
Schizophrenia	18923514	CNVD
Schizophrenia	22241247	CNVD
Mental retardation	21062444	CNVD
Facial dysmorphism	20548289	CNVD
Mental retardation	20548289	CNVD
Schizophrenia	19348701	CNVD
Muscular dystrophy	17160897	CNVD
Cardiomyopathy	17576883	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	22522925	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:3444 , 50 per page) page: 1 2 3 4 5 6 7 ... 69

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:179346000-179355800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr2:179346400-179355800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr2:179346400-179358600	Weak transcription	H9 Cell Line	embryonic stem cell
4	chr2:179346400-179387800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr2:179346600-179356200	Weak transcription	Colonic Mucosa	Colon
6	chr2:179346600-179358600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
7	chr2:179347200-179354400	Weak transcription	Placenta	Placenta
8	chr2:179347200-179355800	Weak transcription	HMEC	breast
9	chr2:179347200-179356000	Weak transcription	H1 Cell Line	embryonic stem cell
10	chr2:179347200-179356000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
11	chr2:179347200-179358600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
12	chr2:179347200-179358600	Weak transcription	NHEK	skin
13	chr2:179347200-179358800	Weak transcription	Placenta Amnion	Placenta Amnion
14	chr2:179347400-179354600	Weak transcription	Rectal Mucosa Donor 29	rectum
15	chr2:179347400-179355200	Weak transcription	Fetal Thymus	thymus
16	chr2:179347400-179356000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
17	chr2:179347400-179356000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
18	chr2:179347400-179363000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
19	chr2:179347400-179369400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
20	chr2:179347600-179351200	Weak transcription	HUES6 Cell Line	embryonic stem cell
21	chr2:179347600-179356000	Weak transcription	HUES48 Cell Line	embryonic stem cell
22	chr2:179347600-179356000	Weak transcription	Fetal Kidney	kidney
23	chr2:179347600-179358400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
24	chr2:179347600-179358600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
25	chr2:179347600-179371000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
26	chr2:179347800-179351600	Weak transcription	Fetal Stomach	stomach
27	chr2:179347800-179353000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
28	chr2:179347800-179355200	Weak transcription	HUES64 Cell Line	embryonic stem cell
29	chr2:179348000-179354000	Weak transcription	Primary neutrophils fromperipheralblood	blood
30	chr2:179348000-179356000	Weak transcription	Thymus	Thymus
31	chr2:179348800-179351800	Weak transcription	Sigmoid Colon	Sigmoid Colon
32	chr2:179348800-179355800	Weak transcription	Spleen	Spleen
33	chr2:179349600-179351800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
34	chr2:179349600-179351800	Weak transcription	Fetal Intestine Small	intestine
35	chr2:179349600-179355000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
36	chr2:179349600-179358600	Weak transcription	Esophagus	oesophagus
37	chr2:179349600-179361200	Strong transcription	Primary T cells from cord blood	blood
38	chr2:179349800-179351400	Weak transcription	Stomach Smooth Muscle	stomach
39	chr2:179349800-179351600	Weak transcription	Cortex derived primary cultured neurospheres	brain
40	chr2:179349800-179354400	Weak transcription	GM12878-XiMat	blood
41	chr2:179349800-179354800	Weak transcription	Left Ventricle	heart
42	chr2:179349800-179355200	Weak transcription	HSMMtube	muscle
43	chr2:179349800-179355400	Weak transcription	NHLF	lung
44	chr2:179349800-179356000	Weak transcription	Aorta	Aorta
45	chr2:179349800-179356000	Weak transcription	Brain Cingulate Gyrus	brain
46	chr2:179349800-179356000	Weak transcription	Ovary	ovary
47	chr2:179349800-179356000	Weak transcription	Psoas Muscle	Psoas
48	chr2:179349800-179356000	Weak transcription	Rectal Smooth Muscle	rectum
49	chr2:179349800-179356000	Weak transcription	Skeletal Muscle Male	skeletal muscle
50	chr2:179349800-179357400	Weak transcription	HUVEC	blood vessel

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