Variant report

Variant	nsv981132
Chromosome Location	chr6:34150971-34162650
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:34157946-34158194	K562	blood:	n/a	n/a
2	ATF2	chr6:34150365-34151392	GM12878	blood:	n/a	n/a
3	ATF3	chr6:34157942-34158246	K562	blood:	n/a	n/a
4	ATF3	chr6:34150419-34151039	GM12878	blood:	n/a	chr6:34150585-34150594
5	BHLHE40	chr6:34158070-34158140	K562	blood:	n/a	n/a
6	CBX3	chr6:34150514-34150974	K562	blood:	n/a	n/a
7	CEBPB	chr6:34150338-34150990	GM12878	blood:	n/a	n/a
8	CTCF	chr6:34158620-34158770	SAEC	small airway:	n/a	chr6:34158686-34158707 chr6:34158698-34158706 chr6:34158691-34158709
9	CTCF	chr6:34158674-34158745	GM19239	blood:	n/a	chr6:34158686-34158707 chr6:34158698-34158706 chr6:34158691-34158709
10	CTCF	chr6:34158620-34158770	GM12865	blood:	n/a	chr6:34158686-34158707 chr6:34158698-34158706 chr6:34158691-34158709
11	CTCF	chr6:34158018-34158197	HepG2	liver:	n/a	n/a
12	CTCF	chr6:34158015-34158237	Spleen_OC	spleen:	n/a	n/a
13	CTCF	chr6:34157980-34158130	K562	blood:	n/a	n/a
14	CTCF	chr6:34158640-34158790	MCF-7	breast:	n/a	chr6:34158686-34158707 chr6:34158698-34158706 chr6:34158691-34158709
15	CTCF	chr6:34158349-34158491	GM10248	blood:	n/a	n/a
16	CTCF	chr6:34158700-34158850	HL-60	blood:	n/a	n/a
17	CTCF	chr6:34158480-34158858	HepG2	liver:	n/a	chr6:34158686-34158707 chr6:34158698-34158706 chr6:34158691-34158709
18	CTCF	chr6:34158013-34158171	GM19238	blood:	n/a	n/a
19	CTCF	chr6:34158620-34158770	Hela-S3	cervix:	n/a	chr6:34158686-34158707 chr6:34158698-34158706 chr6:34158691-34158709
20	CTCF	chr6:34162600-34162750	WI-38	lung:	n/a	chr6:34162732-34162750 chr6:34162733-34162749
21	CTCF	chr6:34158640-34158790	HCPEpiC	choroid plexus:	n/a	chr6:34158686-34158707 chr6:34158698-34158706 chr6:34158691-34158709
22	CTCF	chr6:34158380-34158530	GM06990	blood:	n/a	n/a
23	CTCF	chr6:34158645-34158765	GM19238	blood:	n/a	chr6:34158686-34158707 chr6:34158698-34158706 chr6:34158691-34158709
24	CTCF	chr6:34158740-34158890	GM06990	blood:	n/a	n/a
25	CTCF	chr6:34158020-34158170	GM12874	blood:	n/a	n/a
26	CTCF	chr6:34162620-34162770	Hela-S3	cervix:	n/a	chr6:34162734-34162755 chr6:34162732-34162750 chr6:34162733-34162749
27	CTCF	chr6:34158600-34158750	AG04449	skin:	n/a	chr6:34158686-34158707 chr6:34158698-34158706 chr6:34158691-34158709
28	CTCF	chr6:34158000-34158150	GM12875	blood:	n/a	n/a
29	CTCF	chr6:34158580-34158730	K562	blood:	n/a	chr6:34158686-34158707 chr6:34158698-34158706 chr6:34158691-34158709
30	CTCF	chr6:34162560-34162710	MCF-7	breast:	n/a	n/a
31	CTCF	chr6:34158660-34158810	GM12875	blood:	n/a	chr6:34158686-34158707 chr6:34158698-34158706 chr6:34158691-34158709
32	CTCF	chr6:34158063-34158117	GM10248	blood:	n/a	n/a
33	CTCF	chr6:34158040-34158190	GM12871	blood:	n/a	n/a
34	CTCF	chr6:34158657-34158772	GM12878	blood:	n/a	chr6:34158686-34158707 chr6:34158698-34158706 chr6:34158691-34158709
35	CTCF	chr6:34158680-34158830	HEEpiC	esophagus:	n/a	chr6:34158686-34158707 chr6:34158698-34158706 chr6:34158691-34158709
36	CTCF	chr6:34158554-34158837	MCF-7	breast:	n/a	chr6:34158686-34158707 chr6:34158698-34158706 chr6:34158691-34158709
37	CTCF	chr6:34157985-34158184	HepG2	liver:	n/a	n/a
38	CTCF	chr6:34159509-34159561	GM20000	blood:	n/a	n/a
39	CTCF	chr6:34157978-34158245	GM12878	blood:	n/a	n/a
40	CTCF	chr6:34158620-34158770	HEK293	kidney:	n/a	chr6:34158686-34158707 chr6:34158698-34158706 chr6:34158691-34158709
41	CTCF	chr6:34158007-34158175	MCF-7	breast:	n/a	n/a
42	CTCF	chr6:34158116-34158168	LNCaP	prostate:	n/a	n/a
43	CTCF	chr6:34158663-34158751	GM19240	blood:	n/a	chr6:34158686-34158707 chr6:34158698-34158706 chr6:34158691-34158709
44	CTCF	chr6:34158626-34158781	GM12892	blood:	n/a	chr6:34158686-34158707 chr6:34158698-34158706 chr6:34158691-34158709
45	CTCF	chr6:34157960-34158110	GM12864	blood:	n/a	n/a
46	CTCF	chr6:34162628-34162846	H1-hESC	embryonic stem cell:	n/a	chr6:34162734-34162755 chr6:34162732-34162750 chr6:34162733-34162749
47	CTCF	chr6:34162600-34162750	GM12874	blood:	n/a	chr6:34162732-34162750 chr6:34162733-34162749
48	CTCF	chr6:34158020-34158170	GM12870	blood:	n/a	n/a
49	CTCF	chr6:34158040-34158190	GM12867	blood:	n/a	n/a
50	CTCF	chr6:34158660-34158810	HepG2	liver:	n/a	chr6:34158686-34158707 chr6:34158698-34158706 chr6:34158691-34158709

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:34162022-34162072	H1-hESC	embryonic stem cell:	embryo
2	chr6:34162022-34162072	AG09319	gingival:	n/a
3	chr6:34162022-34162072	T-47D	breast:	n/a
4	chr6:34162022-34162072	MCF10A-Er-Src	breast:	n/a
5	chr6:34162022-34162072	K562	blood:	n/a
6	chr6:34162022-34162072	A549	lung:	n/a
7	chr6:34162022-34162072	HL-60	blood:	n/a
8	chr6:34162022-34162072	NHDF-neo	bronchial:	n/a
9	chr6:34162022-34162072	ECC-1	luminal epithelium:	n/a
10	chr6:34162022-34162072	SAEC	small airway:	n/a
11	chr6:34162022-34162072	IMR90	lung:	fetal
12	chr6:34162022-34162072	NT2-D1	testis:	n/a
13	chr6:34162022-34162072	HRE	kidney:	n/a
14	chr6:34162022-34162072	MCF-7	breast:	n/a
15	chr6:34162022-34162072	GM12891	blood:	n/a
16	chr6:34162022-34162072	HMEC	breast:	n/a
17	chr6:34162022-34162072	HCT-116	colon:	n/a
18	chr6:34162022-34162072	RPTEC	kidney:	n/a
19	chr6:34162022-34162072	HCF	heart:	n/a
20	chr6:34162022-34162072	NB4	blood:	n/a
21	chr6:34162022-34162072	GM06990	blood:	n/a
22	chr6:34162022-34162072	HCM	heart:	n/a
23	chr6:34162022-34162072	Jurkat	blood:	n/a
24	chr6:34162022-34162072	SK-N-SH	brain:	n/a
25	chr6:34162022-34162072	BE2_C	brain:	n/a
26	chr6:34162022-34162072	Caco-2	colon:	n/a
27	chr6:34162022-34162072	AG04449	skin:	fetal
28	chr6:34162022-34162072	HEEpiC	esophagus:	n/a
29	chr6:34162022-34162072	HepG2	liver:	n/a
30	chr6:34162022-34162072	ProgFib	skin:	n/a
31	chr6:34162022-34162072	GM12878	blood:	n/a
32	chr6:34162022-34162072	PFSK-1	brain:	n/a
33	chr6:34162022-34162072	PrEC	prostate:	n/a
34	chr6:34162022-34162072	NHBE	bronchial:	n/a
35	chr6:34162022-34162072	HNPCEpiC	eye:	n/a
36	chr6:34162022-34162072	HRCEpiC	kidney:	n/a
37	chr6:34162022-34162072	NH-A	brain:	n/a
38	chr6:34162022-34162072	SKMC	muscle:	n/a
39	chr6:34162022-34162072	HUVEC	blood vessel:	n/a
40	chr6:34162022-34162072	Hela-S3	cervix:	n/a
41	chr6:34162022-34162072	HCPEpiC	choroid plexus:	n/a
42	chr6:34162022-34162072	AG10803	skin:	n/a
43	chr6:34162022-34162072	CMK	blood:	n/a
44	chr6:34162022-34162072	HRPEpiC	eye:	n/a
45	chr6:34162022-34162072	PANC-1	pancreas:	n/a
46	chr6:34162022-34162072	LNCaP	prostate:	n/a
47	chr6:34162022-34162072	HEK293	kidney:	embryo
48	chr6:34162022-34162072	AG09309	skin:	n/a
49	chr6:34162022-34162072	HPAEpiC	pulmonary alveolar:	n/a
50	chr6:34162022-34162072	GM12892	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr6:34151735..34154399-chr6:34204156..34206128,3	K562	blood:
2	chr6:34148396..34153571-chr6:34214119..34217193,5	K562	blood:
3	chr6:34162251..34164138-chr6:34203896..34205992,2	MCF-7	breast:
4	chr6:34161256..34167016-chr6:34189422..34193988,6	K562	blood:
5	chr6:34149535..34152923-chr6:34209211..34212151,3	K562	blood:
6	chr6:34162257..34164398-chr6:34358966..34361141,2	MCF-7	breast:
7	chr6:34161256..34164388-chr6:34359301..34361572,4	K562	blood:
8	chr6:34151434..34153235-chr6:34202763..34205656,2	K562	blood:
9	chr6:34148072..34149993-chr6:34151430..34154400,2	MCF-7	breast:
10	chr6:34149447..34151035-chr6:34209957..34212126,2	K562	blood:
11	chr6:34150462..34152968-chr6:34158772..34160911,3	K562	blood:
12	chr6:34162021..34165758-chr6:34380623..34387316,6	K562	blood:
13	chr6:34156179..34158888-chr6:34205822..34208269,2	K562	blood:
14	chr6:34162046..34166050-chr6:34204269..34209042,4	MCF-7	breast:
15	chr6:34144149..34151334-chr6:34201235..34205815,9	K562	blood:
16	chr6:34146922..34150986-chr6:34202891..34205942,5	K562	blood:
17	chr6:34151042..34151656-chr8:137407906..137408806,2	MCF-7	breast:
18	chr6:34151808..34154685-chr6:34360088..34362675,2	K562	blood:
19	chr6:34161815..34164629-chr6:34383451..34385385,2	MCF-7	breast:
20	chr6:34150462..34152968-chr6:34158772..34160911,3	K562	blood:
21	chr6:34131296..34132263-chr6:34158158..34158863,4	MCF-7	breast:
22	chr6:34151306..34154507-chr6:34162844..34165811,3	K562	blood:
23	chr6:34160739..34183165-chr6:34199874..34216980,124	K562	blood:
24	chr6:34131271..34132268-chr6:34158042..34159125,4	MCF-7	breast:

Variant related genes	Relation type
KRT18P9	TF binding region
KRT18P9	CpG island
ENSG00000137309	chromatin interactions
ENSG00000272325	chromatin interactions
ENSG00000186577	chromatin interactions

Extended variants
information (count: 546 )
Associated
traits (count: 105 )

Variant overlapped rSNPs/rCNVs (count:546 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs533752481	chr6:34151022-34151023	Weak transcription Flanking Active TSS Enhancers Active TSS ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs79956201	chr6:34151023-34151024	Weak transcription Flanking Active TSS Enhancers Active TSS ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs555041089	chr6:34151037-34151038	Weak transcription Flanking Active TSS Enhancers Active TSS ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs551133916	chr6:34151046-34151047	Weak transcription Flanking Active TSS Enhancers Active TSS ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs571039081	chr6:34151052-34151053	Weak transcription Flanking Active TSS Enhancers Active TSS ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs558675025	chr6:34151083-34151084	Weak transcription Flanking Active TSS Enhancers Active TSS ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs112288494	chr6:34151135-34151136	Weak transcription Flanking Active TSS Enhancers Active TSS ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs370758802	chr6:34151185-34151186	Weak transcription Flanking Active TSS Enhancers Active TSS ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs141399874	chr6:34151194-34151195	Weak transcription Flanking Active TSS Enhancers Active TSS ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs202220843	chr6:34151196-34151197	Weak transcription Flanking Active TSS Enhancers Active TSS ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs200504846	chr6:34151198-34151199	Weak transcription Flanking Active TSS Enhancers Active TSS ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs58944776	chr6:34151199-34151200	Weak transcription Flanking Active TSS Enhancers Active TSS ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs200092145	chr6:34151200-34151201	Weak transcription Flanking Active TSS Enhancers Active TSS ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs201018400	chr6:34151201-34151202	Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs9469734	chr6:34151206-34151207	Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs374244024	chr6:34151355-34151356	Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs199776000	chr6:34151385-34151386	Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs139599289	chr6:34151395-34151396	Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs185988455	chr6:34151429-34151430	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs142889624	chr6:34151514-34151515	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs191702356	chr6:34151553-34151554	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs10807135	chr6:34151564-34151565	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs540660269	chr6:34151582-34151583	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs561923441	chr6:34151583-34151584	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs372166447	chr6:34151755-34151756	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs544669043	chr6:34151762-34151763	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs563081156	chr6:34151805-34151806	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs533530258	chr6:34151806-34151807	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs551807993	chr6:34151857-34151858	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs375560617	chr6:34151860-34151861	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs367599972	chr6:34151862-34151863	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs371852089	chr6:34151870-34151871	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs35147500	chr6:34151890-34151891	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs549010219	chr6:34151893-34151894	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs151034135	chr6:34151901-34151902	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs374800697	chr6:34151924-34151925	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs13212862	chr6:34151935-34151936	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs536733968	chr6:34151940-34151941	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs369184854	chr6:34151944-34151945	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs538476126	chr6:34151946-34151947	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs11969452	chr6:34151947-34151948	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs9394196	chr6:34151952-34151953	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs375538485	chr6:34151960-34151961	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs191022931	chr6:34151963-34151964	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs555732997	chr6:34151964-34151965	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs574040564	chr6:34151970-34151971	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs544734817	chr6:34151992-34151993	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs374063946	chr6:34152016-34152017	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs578129181	chr6:34152023-34152024	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs545618104	chr6:34152029-34152030	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:105)

Disease	PMID	Source
Follicular lymphoma	20505157	CNVD
Glioblastoma multiforme	21080181	CNVD
Ewing''s sarcoma	21437220	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Leukemia	21518781	CNVD
Cancer	21637783	CNVD
Facial dysmorphism	22105932	CNVD
Medulloblastoma	21979893	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Endometrial cancer	22040021	CNVD
Acute myeloid leukemia	16864856	CNVD
Breast cancer	21264507	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	16751803	CNVD
Bladder cancer	19088036	CNVD
Wilms tumour	21544195	CNVD
Uveal melanoma	21693616	CNVD
Biliary cancer	19435499	CNVD
Malaria	21533027	CNVD
Retinoblastoma	19183342	CNVD
Acute myeloid leukemia	20729466	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21858162	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	21448237	CNVD
Melanoma	18172304	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Hepatocellular carcinoma	16750200	CNVD
Autism	22495311	CNVD
Cancer	16790693	CNVD
Cervical cancer	21062161	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Systemic lupus erythematosus	17503323	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Urothelial carcinoma	18382360	CNVD
Cancer	21183584	CNVD
Hodgkin''s lymphoma	17606441	CNVD
small cell lung cancer	20016488	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Gastric cancer	17908304	CNVD
Metanephric adenoma	20802469	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Schizophrenia	19571808	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Neuroblastoma	16790693	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Breast cancer	16397240	CNVD
Retinoblastoma	22278416	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Systemic lupus erythematosus	20877625	CNVD
Cleidocranial dysplasia	18696259	CNVD
Holoprosencephaly	21359414	CNVD
Liposarcoma	21253554	CNVD
Uveal melanoma	20484589	CNVD
Fibroblasts	20926602	CNVD
Systemic lupus erythematosus	19279649	CNVD
Retinoblastoma	16790693	CNVD
Acute myocardial infarction	18032375	CNVD
Renal cell carcinoma	19150565	CNVD
Systemic lupus erythematosus	19591781	CNVD
Attention deficit hyperactivity disorder	19287146	CNVD
Autism	19287146	CNVD
Erythema nodosum in leprosy	19287146	CNVD
Henoch-schoenlein purpura	19287146	CNVD
Liver cirrhosis	19287146	CNVD
Systemic lupus erythematosus	19287146	CNVD
Autoimmune disease	19135723	CNVD
Congenital adrenal hyperplasia	18478071	CNVD
Systemic lupus erythematosus	19287147	CNVD
Osteosarcoma	16790693	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
Cancer	22183965	CNVD
Melanoma	22183965	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Lung cancer	18438408	CNVD
Glioblastoma multiforme	21138945	CNVD
Breast cancer	21364760	CNVD
Urothelial carcinoma	21177765	CNVD
Basal cell lymphoma	19029149	CNVD
Diffuse large b-cell lymphoma	19029149	CNVD
Myelofibrosis	22110671	CNVD
Liver carcinoma	19366792	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:106 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:34147400-34162800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr6:34149400-34151800	Enhancers	Primary T killer naive cells fromperipheralblood	blood
3	chr6:34149600-34151200	Enhancers	Primary T regulatory cells fromperipheralblood	blood
4	chr6:34149600-34151400	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
5	chr6:34149800-34151400	Enhancers	Primary hematopoietic stem cells short term culture	blood
6	chr6:34149800-34151600	ZNF genes & repeats	GM12878-XiMat	blood
7	chr6:34150000-34151000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
8	chr6:34150200-34151000	Active TSS	Rectal Mucosa Donor 29	rectum
9	chr6:34150200-34151200	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
10	chr6:34150200-34151600	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
11	chr6:34150400-34151400	Flanking Active TSS	Primary B cells from peripheral blood	blood
12	chr6:34150400-34151400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
13	chr6:34150600-34151000	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
14	chr6:34150600-34151200	Flanking Active TSS	Primary B cells from cord blood	blood
15	chr6:34150600-34151200	Flanking Active TSS	Primary T cells from cord blood	blood
16	chr6:34150600-34151200	Flanking Active TSS	Primary T cells fromperipheralblood	blood
17	chr6:34150600-34151200	Flanking Active TSS	Primary T helper memory cells from peripheral blood 2	blood
18	chr6:34150600-34151200	Flanking Active TSS	Primary T helper memory cells from peripheral blood 1	blood
19	chr6:34150600-34151200	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
20	chr6:34150600-34151200	Flanking Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
21	chr6:34150600-34151200	Flanking Active TSS	Primary Natural Killer cells fromperipheralblood	blood
22	chr6:34150600-34151200	Flanking Active TSS	Primary T killer memory cells from peripheral blood	blood
23	chr6:34150600-34151200	Active TSS	Duodenum Mucosa	Duodenum
24	chr6:34150600-34151200	Flanking Active TSS	Fetal Thymus	thymus
25	chr6:34150600-34151200	Flanking Active TSS	Thymus	Thymus
26	chr6:34150600-34151400	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
27	chr6:34150600-34151400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
28	chr6:34150600-34151400	Flanking Active TSS	Dnd41	blood
29	chr6:34150800-34151200	Flanking Active TSS	Primary monocytes fromperipheralblood	blood
30	chr6:34150800-34151200	Flanking Active TSS	Primary T helper naive cells fromperipheralblood	blood
31	chr6:34150800-34151200	Enhancers	HUVEC	blood vessel
32	chr6:34150800-34151400	Flanking Active TSS	Primary T helper naive cells from peripheral blood	blood
33	chr6:34151000-34151200	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
34	chr6:34151000-34151200	Flanking Active TSS	Rectal Mucosa Donor 29	rectum
35	chr6:34151000-34163800	Weak transcription	Right Atrium	heart
36	chr6:34151200-34151400	Active TSS	Primary neutrophils fromperipheralblood	blood
37	chr6:34151200-34151400	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
38	chr6:34151200-34151400	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
39	chr6:34151200-34151400	Enhancers	Primary T killer memory cells from peripheral blood	blood
40	chr6:34151200-34151400	Enhancers	Fetal Thymus	thymus
41	chr6:34151200-34151400	Enhancers	Thymus	Thymus
42	chr6:34151200-34151600	Enhancers	Primary T cells from cord blood	blood
43	chr6:34151200-34151800	Enhancers	Primary monocytes fromperipheralblood	blood
44	chr6:34151200-34151800	Enhancers	Primary B cells from cord blood	blood
45	chr6:34151200-34151800	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
46	chr6:34151200-34151800	Enhancers	Primary T helper cells fromperipheralblood	blood
47	chr6:34151200-34151800	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
48	chr6:34151200-34152000	Enhancers	Primary T cells fromperipheralblood	blood
49	chr6:34151200-34152800	Enhancers	Primary T helper naive cells fromperipheralblood	blood
50	chr6:34151200-34163800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood

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