Variant report

Variant	nsv464140
Chromosome Location	chr6:167426681-167492552
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:713)
CpG islands
(count:366)
Chromatin interactive
region (count:37)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:713 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr6:167469880-167470220	GM12878	blood:	n/a	n/a
2	ATF2	chr6:167460900-167461576	GM12878	blood:	n/a	n/a
3	ATF2	chr6:167461011-167461462	GM12878	blood:	n/a	n/a
4	BACH1	chr6:167440490-167440592	K562	blood:	n/a	n/a
5	BACH1	chr6:167438242-167438243	K562	blood:	n/a	n/a
6	BATF	chr6:167444821-167445080	GM12878	blood:	n/a	n/a
7	BATF	chr6:167469888-167470180	GM12878	blood:	n/a	chr6:167470148-167470158
8	BATF	chr6:167469899-167470221	GM12878	blood:	n/a	chr6:167470148-167470158
9	BATF	chr6:167461075-167461391	GM12878	blood:	n/a	n/a
10	BATF	chr6:167460966-167461486	GM12878	blood:	n/a	n/a
11	BCL11A	chr6:167461087-167461382	GM12878	blood:	n/a	n/a
12	BCL11A	chr6:167461029-167461436	GM12878	blood:	n/a	n/a
13	BCL11A	chr6:167469910-167470220	GM12878	blood:	n/a	n/a
14	BCL11A	chr6:167469903-167470188	GM12878	blood:	n/a	n/a
15	BCLAF1	chr6:167460917-167461504	GM12878	blood:	n/a	n/a
16	BCLAF1	chr6:167454620-167455156	GM12878	blood:	n/a	n/a
17	BHLHE40	chr6:167460597-167461438	GM12878	blood:	n/a	chr6:167460781-167460790
18	BHLHE40	chr6:167454756-167455139	K562	blood:	n/a	n/a
19	BHLHE40	chr6:167454726-167455208	GM12878	blood:	n/a	n/a
20	BHLHE40	chr6:167491115-167491316	HepG2	liver:	n/a	n/a
21	CEBPB	chr6:167479230-167479550	IMR90	lung:	n/a	chr6:167479379-167479390
22	CEBPB	chr6:167460854-167461567	GM12878	blood:	n/a	n/a
23	CEBPB	chr6:167459409-167459552	HepG2	liver:	n/a	n/a
24	CEBPB	chr6:167461929-167462140	A549	lung:	n/a	chr6:167461979-167461990
25	CEBPB	chr6:167479218-167479540	HepG2	liver:	n/a	chr6:167479379-167479390
26	CEBPB	chr6:167487306-167487449	H1-hESC	embryonic stem cell:	n/a	chr6:167487340-167487351
27	CEBPB	chr6:167459360-167459724	MCF-7	breast:	n/a	n/a
28	CEBPB	chr6:167445915-167446133	K562	blood:	n/a	n/a
29	CEBPB	chr6:167461917-167462126	HepG2	liver:	n/a	chr6:167461979-167461990
30	CEBPB	chr6:167479236-167479443	K562	blood:	n/a	chr6:167479379-167479390
31	CEBPB	chr6:167479281-167479541	A549	lung:	n/a	chr6:167479379-167479390
32	CEBPB	chr6:167457264-167457570	HepG2	liver:	n/a	n/a
33	CEBPB	chr6:167487230-167487495	HepG2	liver:	n/a	chr6:167487340-167487351
34	CHD1	chr6:167491818-167491826	GM12878	blood:	n/a	n/a
35	CHD1	chr6:167460409-167461483	GM12878	blood:	n/a	n/a
36	CHD1	chr6:167454747-167455089	GM12878	blood:	n/a	n/a
37	CHD2	chr6:167489899-167490084	HepG2	liver:	n/a	n/a
38	CHD2	chr6:167460837-167461471	GM12878	blood:	n/a	n/a
39	CHD2	chr6:167492252-167492258	GM12878	blood:	n/a	n/a
40	CREB1	chr6:167460867-167461525	GM12878	blood:	n/a	n/a
41	CREB1	chr6:167460871-167461646	GM12878	blood:	n/a	n/a
42	CTCF	chr6:167447780-167447930	HepG2	liver:	n/a	n/a
43	CTCF	chr6:167460532-167460541	GM10248	blood:	n/a	n/a
44	CTCF	chr6:167459461-167459588	LNCaP	prostate:	n/a	chr6:167459565-167459573
45	CTCF	chr6:167459440-167459590	GM12870	blood:	n/a	chr6:167459565-167459573
46	CTCF	chr6:167459460-167459610	HCFaa	heart:	n/a	chr6:167459565-167459573
47	CTCF	chr6:167459480-167459630	RPTEC	kidney:	n/a	chr6:167459565-167459573
48	CTCF	chr6:167459480-167459630	GM12873	blood:	n/a	chr6:167459565-167459573
49	CTCF	chr6:167458340-167458490	HepG2	liver:	n/a	n/a
50	CTCF	chr6:167454867-167454975	GM12892	blood:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:167453801-167453851	NT2-D1	testis:	n/a
2	chr6:167432504-167432554	MCF-7	breast:	n/a
3	chr6:167453801-167453851	HRPEpiC	eye:	n/a
4	chr6:167432531-167432581	Caco-2	colon:	n/a
5	chr6:167453801-167453851	HMEC	breast:	n/a
6	chr6:167432531-167432581	NHBE	bronchial:	n/a
7	chr6:167432504-167432554	MCF10A-Er-Src	breast:	n/a
8	chr6:167490870-167490920	NHDF-neo	bronchial:	n/a
9	chr6:167490870-167490920	PFSK-1	brain:	n/a
10	chr6:167490980-167491030	ECC-1	luminal epithelium:	n/a
11	chr6:167432504-167432554	ProgFib	skin:	n/a
12	chr6:167490870-167490920	HEK293	kidney:	embryo
13	chr6:167490980-167491030	Hepatocyte	liver:	n/a
14	chr6:167432531-167432581	SK-N-SH	brain:	n/a
15	chr6:167490870-167490920	GM06990	blood:	n/a
16	chr6:167490980-167491030	LNCaP	prostate:	n/a
17	chr6:167490870-167490920	Hela-S3	cervix:	n/a
18	chr6:167453801-167453851	HRE	kidney:	n/a
19	chr6:167432531-167432581	BE2_C	brain:	n/a
20	chr6:167490870-167490920	AG04450	lung:	fetal
21	chr6:167432531-167432581	HMEC	breast:	n/a
22	chr6:167453801-167453851	HL-60	blood:	n/a
23	chr6:167490870-167490920	T-47D	breast:	n/a
24	chr6:167432566-167432616	AG04450	lung:	fetal
25	chr6:167490980-167491030	BE2_C	brain:	n/a
26	chr6:167432504-167432554	AoSMC	blood vessel:	n/a
27	chr6:167432566-167432616	AG09309	skin:	n/a
28	chr6:167432566-167432616	HPAEpiC	pulmonary alveolar:	n/a
29	chr6:167432531-167432581	K562	blood:	n/a
30	chr6:167432566-167432616	Caco-2	colon:	n/a
31	chr6:167490980-167491030	NT2-D1	testis:	n/a
32	chr6:167432566-167432616	PANC-1	pancreas:	n/a
33	chr6:167453801-167453851	RPTEC	kidney:	n/a
34	chr6:167432531-167432581	PFSK-1	brain:	n/a
35	chr6:167432531-167432581	HRPEpiC	eye:	n/a
36	chr6:167432504-167432554	SK-N-SH_RA	brain:	n/a
37	chr6:167453801-167453851	MCF-7	breast:	n/a
38	chr6:167490980-167491030	NHBE	bronchial:	n/a
39	chr6:167432531-167432581	AoSMC	blood vessel:	n/a
40	chr6:167432504-167432554	AG04449	skin:	fetal
41	chr6:167432566-167432616	AG10803	skin:	n/a
42	chr6:167432566-167432616	SK-N-SH	brain:	n/a
43	chr6:167432566-167432616	ovcar-3	ovarian:	n/a
44	chr6:167490870-167490920	K562	blood:	n/a
45	chr6:167432531-167432581	ovcar-3	ovarian:	n/a
46	chr6:167453801-167453851	Hepatocyte	liver:	n/a
47	chr6:167432566-167432616	HAEpiC	amniotic membrane:	n/a
48	chr6:167490870-167490920	GM12878	blood:	n/a
49	chr6:167490870-167490920	AG10803	skin:	n/a
50	chr6:167432504-167432554	AG10803	skin:	n/a

(count:37 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:167382648..167385296-chr6:167441304..167444220,2	K562	blood:
2	chr6:167428569..167431228-chr6:167442588..167444802,2	K562	blood:
3	chr6:167441965..167443908-chr6:167444261..167446569,2	MCF-7	breast:
4	chr6:167433967..167440072-chr6:167441363..167445632,6	K562	blood:
5	chr6:167422410..167425516-chr6:167426454..167429181,4	K562	blood:
6	chr6:167446559..167451164-chr6:167453044..167456262,4	K562	blood:
7	chr6:167424149..167427118-chr6:167441953..167443823,2	K562	blood:
8	chr6:167453011..167457183-chr6:167458189..167461851,4	K562	blood:
9	chr6:167438329..167440773-chr6:167442829..167444419,2	K562	blood:
10	chr6:167420630..167423584-chr6:167426285..167427998,2	MCF-7	breast:
11	chr6:167423442..167425516-chr6:167426454..167430057,4	K562	blood:
12	chr6:167441965..167443908-chr6:167444261..167446569,2	MCF-7	breast:
13	chr6:167438895..167441335-chr6:167445093..167449039,4	K562	blood:
14	chr6:167442856..167445565-chr6:167449588..167451484,2	K562	blood:
15	chr6:167459004..167459905-chr6:167555024..167555917,3	MCF-7	breast:
16	chr6:167410797..167412644-chr6:167437633..167439150,2	MCF-7	breast:
17	chr6:167428569..167431228-chr6:167442588..167444802,2	K562	blood:
18	chr6:167438895..167441335-chr6:167445093..167449039,4	K562	blood:
19	chr6:167200327..167200836-chr6:167459295..167459843,2	K562	blood:
20	chr6:167438329..167440773-chr6:167442829..167444419,2	K562	blood:
21	chr6:167426218..167428514-chr6:167429903..167432841,2	K562	blood:
22	chr6:167188018..167188945-chr6:167458801..167459761,3	MCF-7	breast:
23	chr6:167426218..167428514-chr6:167429903..167432841,2	K562	blood:
24	chr6:167424149..167427118-chr6:167441953..167443823,2	K562	blood:
25	chr6:167150380..167152971-chr6:167466714..167468496,2	K562	blood:
26	chr6:167411246..167413456-chr6:167456024..167457540,2	K562	blood:
27	chr6:167368878..167371714-chr6:167425484..167428266,2	K562	blood:
28	chr6:167446559..167451164-chr6:167453044..167456262,4	K562	blood:
29	chr6:167442856..167445565-chr6:167449588..167451484,2	K562	blood:
30	chr6:167433511..167435298-chr6:167462855..167465719,2	K562	blood:
31	chr6:167410835..167412636-chr6:167439042..167441228,2	K562	blood:
32	chr6:167433967..167438012-chr6:167438507..167442863,4	K562	blood:
33	chr6:167487932..167489942-chr6:167492963..167495055,2	K562	blood:
34	chr6:167433511..167435298-chr6:167462855..167465719,2	K562	blood:
35	chr6:167454169..167455868-chr6:167473255..167476211,2	K562	blood:
36	chr6:167454169..167455868-chr6:167473255..167476211,2	K562	blood:
37	chr6:167453011..167457183-chr6:167458189..167461851,4	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FGFR1OP-8	chr6:167465448-167466347	NONHSAT116076

No data

Variant related genes	Relation type
FGFR1OP	TF binding region
FGFR1OP	CpG island
ENSG00000249141	chromatin interactions
ENSG00000227598	chromatin interactions
ENSG00000272980	chromatin interactions
ENSG00000213066	chromatin interactions
ENSG00000026297	chromatin interactions
ENSG00000265828	chromatin interactions

Extended variants
information (count: 2231 )
Associated
traits (count: 84 )

Variant overlapped rSNPs/rCNVs (count:2231 , 50 per page) page: 1 2 3 4 5 6 7 ... 45

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs9457250	chr6:167426681-167426682	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs372212157	chr6:167426702-167426703	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs9457251	chr6:167426707-167426708	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
4	rs77957971	chr6:167426870-167426871	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs539260729	chr6:167426884-167426885	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs562687993	chr6:167426902-167426903	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs368856649	chr6:167426937-167426938	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs371988305	chr6:167426953-167426954	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs376560264	chr6:167426959-167426960	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs530137260	chr6:167426976-167426977	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs182726034	chr6:167426985-167426986	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs369501965	chr6:167427022-167427023	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs373387476	chr6:167427034-167427035	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs377486279	chr6:167427035-167427036	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs34617108	chr6:167427045-167427046	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs73026233	chr6:167427080-167427081	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs369921670	chr6:167427089-167427090	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs144952423	chr6:167427106-167427107	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs370219340	chr6:167427127-167427128	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs554996802	chr6:167427199-167427200	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs576350331	chr6:167427200-167427201	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs75165982	chr6:167427232-167427233	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs142069305	chr6:167427331-167427332	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs151152251	chr6:167427334-167427335	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs191644840	chr6:167427359-167427360	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs559896628	chr6:167427375-167427376	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs527609376	chr6:167427378-167427379	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs549002370	chr6:167427388-167427389	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs576763569	chr6:167427448-167427449	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs74709214	chr6:167427478-167427479	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs531212734	chr6:167427507-167427508	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs552869270	chr6:167427512-167427513	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs549777647	chr6:167427560-167427561	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs571383330	chr6:167427588-167427589	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs571047770	chr6:167427598-167427599	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs532232150	chr6:167427647-167427648	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs538480119	chr6:167427687-167427688	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs548038792	chr6:167427735-167427736	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs75825898	chr6:167427769-167427770	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs140069700	chr6:167427779-167427780	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs554973781	chr6:167427782-167427783	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs556485865	chr6:167427790-167427791	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs537068979	chr6:167427807-167427808	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs377441805	chr6:167427808-167427809	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs558489029	chr6:167427816-167427817	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs568632065	chr6:167427819-167427820	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs162284	chr6:167427845-167427846	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs118137167	chr6:167427918-167427919	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs113333815	chr6:167427965-167427966	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs112081631	chr6:167427974-167427975	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:84)

Disease	PMID	Source
Uveal melanoma	21693616	CNVD
Glioblastoma multiforme	21080181	CNVD
Biliary cancer	19435499	CNVD
Medulloblastoma	21979893	CNVD
Malaria	21533027	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Ewing''s sarcoma	17952124	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
Acute lymphoblastic leukemia	22237106	CNVD
Neuroblastoma	18923191	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Melanoma	18172304	CNVD
Cancer	21637783	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Follicular lymphoma	19010834	CNVD
Non-small cell lung cancer	21044232	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	16608533	CNVD
Non-small cell lung cancer	21385341	CNVD
Prostate cancer	16705090	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Colorectal cancer	16272173	CNVD
Ependymoma	16718352	CNVD
Gastric cancer	17908304	CNVD
High-proliferative meningiomas	17937814	CNVD
Intracranial tumor	16823260	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	16272173	CNVD
Wilms tumour	21544195	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Malignant melanoma	18718029	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Breast cancer	21858162	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	17603634	CNVD
Developmental delay	19490664	CNVD
Burkitt''s lymphoma	18698080	CNVD
Neurodevelopmental disorder	22521361	CNVD
small cell lung cancer	20016488	CNVD
Adenoid cystic carcinoma	18698036	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Leukemia	18688285	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Prostate cancer	18632612	CNVD
Lung cancer	18438408	CNVD
Burkitt''s lymphoma	19759907	CNVD
Esophageal cancer	21851588	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Breast cancer	17133270	CNVD
Testicular germ cell tumor	18059402	CNVD
Chordoma	18071362	CNVD
Glioblastoma multiforme	19435819	CNVD
Developmental delay	21147756	CNVD
Ovarian cancer	21720365	CNVD
abnormal development	18461090	CNVD
Epilepsy	22083797	CNVD
Myelofibrosis	22110671	CNVD
chordoma	19801981	CNVD
Myxofibrosarcoma	16751306	CNVD
Autism	17483303	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Acute myeloid leukemia	19651601	CNVD
Sudden cardiac death	19188705	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD

Chromatin state (count:1428 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:167413600-167428600	Weak transcription	Aorta	Aorta
2	chr6:167413600-167428800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
3	chr6:167413600-167428800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr6:167413600-167438800	Weak transcription	Right Ventricle	heart
5	chr6:167413600-167449200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
6	chr6:167413600-167452400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
7	chr6:167413800-167436800	Weak transcription	HSMMtube	muscle
8	chr6:167414600-167428600	Weak transcription	Fetal Brain Male	brain
9	chr6:167414600-167429200	Strong transcription	HUES48 Cell Line	embryonic stem cell
10	chr6:167414600-167429200	Strong transcription	Primary B cells from cord blood	blood
11	chr6:167414600-167430400	Strong transcription	iPS-18 Cell Line	embryonic stem cell
12	chr6:167414600-167433200	Strong transcription	HUES6 Cell Line	embryonic stem cell
13	chr6:167414600-167440800	Strong transcription	iPS-20b Cell Line	embryonic stem cell
14	chr6:167414600-167441000	Weak transcription	Psoas Muscle	Psoas
15	chr6:167414600-167448000	Weak transcription	Small Intestine	intestine
16	chr6:167414600-167450200	Weak transcription	Stomach Mucosa	stomach
17	chr6:167415200-167440800	Strong transcription	HUES64 Cell Line	embryonic stem cell
18	chr6:167415400-167454000	Strong transcription	Fetal Thymus	thymus
19	chr6:167415400-167456600	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
20	chr6:167416000-167444600	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
21	chr6:167416200-167431800	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
22	chr6:167416200-167437400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
23	chr6:167417200-167455400	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
24	chr6:167417600-167443000	Strong transcription	Primary monocytes fromperipheralblood	blood
25	chr6:167417600-167446000	Strong transcription	Dnd41	blood
26	chr6:167417600-167454800	Strong transcription	Primary hematopoietic stem cells short term culture	blood
27	chr6:167417800-167429200	Strong transcription	Primary T cells fromperipheralblood	blood
28	chr6:167417800-167455200	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
29	chr6:167418800-167429200	Strong transcription	Osteobl	bone
30	chr6:167419200-167432800	Strong transcription	Fetal Muscle Leg	muscle
31	chr6:167419600-167431200	Weak transcription	Right Atrium	heart
32	chr6:167419600-167439000	Weak transcription	Colon Smooth Muscle	Colon
33	chr6:167419600-167440000	Weak transcription	Fetal Heart	heart
34	chr6:167420000-167436400	Weak transcription	Colonic Mucosa	Colon
35	chr6:167420200-167428800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
36	chr6:167420800-167428600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
37	chr6:167420800-167428600	Weak transcription	NHEK	skin
38	chr6:167420800-167447600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
39	chr6:167421000-167432400	Weak transcription	Skeletal Muscle Male	skeletal muscle
40	chr6:167422400-167433200	Strong transcription	Fetal Intestine Large	intestine
41	chr6:167422600-167428600	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
42	chr6:167423000-167446400	Strong transcription	HepG2	liver
43	chr6:167423000-167457600	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
44	chr6:167423400-167427200	Strong transcription	Rectal Mucosa Donor 29	rectum
45	chr6:167423400-167429200	Strong transcription	Primary hematopoietic stem cells	blood
46	chr6:167423400-167430200	Strong transcription	GM12878-XiMat	blood
47	chr6:167423400-167446400	Strong transcription	Liver	Liver
48	chr6:167423400-167452200	Strong transcription	Monocytes-CD14+_RO01746	blood
49	chr6:167423600-167427400	Strong transcription	Duodenum Mucosa	Duodenum
50	chr6:167423600-167430400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--

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