Variant report

Variant	esv3349532
Chromosome Location	chr1:85154814-85157812
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:711)
CpG islands
(count:856)
Chromatin interactive
region (count:14)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:711 , 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	ARID3A	chr1:85155236-85155632	K562	blood:	n/a	n/a
2	ARID3A	chr1:85153651-85154912	K562	blood:	n/a	n/a
3	ARID3A	chr1:85157229-85157238	K562	blood:	n/a	n/a
4	ARID3A	chr1:85156098-85156204	K562	blood:	n/a	n/a
5	ATF1	chr1:85155413-85156571	K562	blood:	n/a	n/a
6	ATF3	chr1:85155852-85156197	K562	blood:	n/a	n/a
7	BACH1	chr1:85155050-85155317	K562	blood:	n/a	n/a
8	BACH1	chr1:85155464-85155790	H1-hESC	embryonic stem cell:	n/a	n/a
9	BACH1	chr1:85157074-85157185	K562	blood:	n/a	n/a
10	BACH1	chr1:85156270-85157052	H1-hESC	embryonic stem cell:	n/a	n/a
11	BCLAF1	chr1:85156203-85156654	GM12878	blood:	n/a	n/a
12	BHLHE40	chr1:85156157-85156595	HepG2	liver:	n/a	chr1:85156164-85156180
13	BHLHE40	chr1:85156023-85156774	GM12878	blood:	n/a	chr1:85156164-85156180
14	BHLHE40	chr1:85156025-85157255	K562	blood:	n/a	chr1:85156164-85156180
15	BRCA1	chr1:85156341-85156423	Hela-S3	cervix:	n/a	n/a
16	CBX3	chr1:85155941-85156577	K562	blood:	n/a	n/a
17	CCNT2	chr1:85155543-85156769	K562	blood:	n/a	chr1:85156184-85156193 chr1:85156503-85156512 chr1:85156473-85156482
18	CEBPB	chr1:85155489-85155881	Hela-S3	cervix:	n/a	n/a
19	CEBPB	chr1:85153886-85154897	K562	blood:	n/a	n/a
20	CEBPB	chr1:85153852-85154879	K562	blood:	n/a	n/a
21	CEBPB	chr1:85156123-85156572	Hela-S3	cervix:	n/a	n/a
22	CEBPD	chr1:85154227-85154850	K562	blood:	n/a	n/a
23	CEBPD	chr1:85154207-85154859	K562	blood:	n/a	n/a
24	CEBPD	chr1:85155801-85156626	HepG2	liver:	n/a	n/a
25	CHD1	chr1:85156596-85157143	H1-hESC	embryonic stem cell:	n/a	n/a
26	CHD1	chr1:85155175-85155778	H1-hESC	embryonic stem cell:	n/a	n/a
27	CHD2	chr1:85156157-85156615	HepG2	liver:	n/a	chr1:85156471-85156481
28	CHD2	chr1:85155398-85156648	Hela-S3	cervix:	n/a	chr1:85156471-85156481 chr1:85156140-85156150
29	CHD2	chr1:85155610-85156884	GM12878	blood:	n/a	chr1:85156471-85156481 chr1:85156140-85156150
30	CHD2	chr1:85155640-85156898	H1-hESC	embryonic stem cell:	n/a	chr1:85156471-85156481 chr1:85156140-85156150
31	CHD2	chr1:85155741-85155869	HepG2	liver:	n/a	n/a
32	CHD2	chr1:85155791-85156753	K562	blood:	n/a	chr1:85156471-85156481 chr1:85156140-85156150
33	CREB1	chr1:85155586-85156840	K562	blood:	n/a	n/a
34	CREB1	chr1:85155559-85156663	H1-hESC	embryonic stem cell:	n/a	n/a
35	CREB1	chr1:85155774-85156791	HepG2	liver:	n/a	n/a
36	CREB1	chr1:85155536-85156635	H1-hESC	embryonic stem cell:	n/a	n/a
37	CREB1	chr1:85155542-85156681	HepG2	liver:	n/a	n/a
38	CREB1	chr1:85155797-85156294	ECC-1	luminal epithelium:	n/a	n/a
39	CREB1	chr1:85155861-85156675	A549	lung:	n/a	n/a
40	CREB1	chr1:85155997-85156231	A549	lung:	n/a	n/a
41	CREB1	chr1:85153810-85154880	K562	blood:	n/a	n/a
42	CREB1	chr1:85155416-85156629	GM12878	blood:	n/a	n/a
43	CREB1	chr1:85155633-85156665	K562	blood:	n/a	n/a
44	CTCF	chr1:85155520-85155670	GM12873	blood:	n/a	n/a
45	CTCF	chr1:85155380-85155530	MCF-7	breast:	n/a	n/a
46	CTCF	chr1:85155556-85155686	GM10266	blood:	n/a	n/a
47	CTCF	chr1:85155520-85155670	HMF	breast:	n/a	n/a
48	CTCF	chr1:85155532-85155683	SK-N-SH_RA	brain:	n/a	n/a
49	CTCF	chr1:85155500-85155650	HPAF	blood vessel:	n/a	n/a
50	CTCF	chr1:85155520-85155670	AG09309	skin:	n/a	n/a

(count:856 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:85156638-85156688	AoSMC	blood vessel:	n/a
2	chr1:85156266-85156316	K562	blood:	n/a
3	chr1:85156638-85156688	AoSMC	blood vessel:	n/a
4	chr1:85156266-85156316	K562	blood:	n/a
5	chr1:85156797-85156847	PFSK-1	brain:	n/a
6	chr1:85155724-85155774	HIPEpiC	eye:	n/a
7	chr1:85156797-85156847	HEK293	kidney:	embryo
8	chr1:85156566-85156616	MCF-7	breast:	n/a
9	chr1:85156566-85156616	HPAEpiC	pulmonary alveolar:	n/a
10	chr1:85156430-85156480	RPTEC	kidney:	n/a
11	chr1:85157327-85157377	MCF-7	breast:	n/a
12	chr1:85157327-85157377	HepG2	liver:	n/a
13	chr1:85156430-85156480	HCPEpiC	choroid plexus:	n/a
14	chr1:85156430-85156480	NHBE	bronchial:	n/a
15	chr1:85156370-85156420	H1-hESC	embryonic stem cell:	embryo
16	chr1:85155548-85155598	AG10803	skin:	n/a
17	chr1:85155606-85155656	GM12891	blood:	n/a
18	chr1:85157183-85157233	HCT-116	colon:	n/a
19	chr1:85156187-85156237	U87	brain:	n/a
20	chr1:85156797-85156847	HCM	heart:	n/a
21	chr1:85156566-85156616	SK-N-SH	brain:	n/a
22	chr1:85157183-85157233	Hela-S3	cervix:	n/a
23	chr1:85156430-85156480	K562	blood:	n/a
24	chr1:85156797-85156847	SK-N-SH_RA	brain:	n/a
25	chr1:85156370-85156420	Hela-S3	cervix:	n/a
26	chr1:85155724-85155774	MCF-7	breast:	n/a
27	chr1:85156634-85156684	HRCEpiC	kidney:	n/a
28	chr1:85157327-85157377	GM12892	blood:	n/a
29	chr1:85156638-85156688	AG09309	skin:	n/a
30	chr1:85156638-85156688	HPAEpiC	pulmonary alveolar:	n/a
31	chr1:85157327-85157377	HPAEpiC	pulmonary alveolar:	n/a
32	chr1:85156566-85156616	PFSK-1	brain:	n/a
33	chr1:85156797-85156847	K562	blood:	n/a
34	chr1:85156638-85156688	SK-N-MC	brain:	n/a
35	chr1:85157327-85157377	SK-N-SH_RA	brain:	n/a
36	chr1:85155724-85155774	HEEpiC	esophagus:	n/a
37	chr1:85156638-85156688	H1-hESC	embryonic stem cell:	embryo
38	chr1:85156266-85156316	PANC-1	pancreas:	n/a
39	chr1:85155724-85155774	Hela-S3	cervix:	n/a
40	chr1:85155724-85155774	SAEC	small airway:	n/a
41	chr1:85155724-85155774	HRE	kidney:	n/a
42	chr1:85156566-85156616	HCPEpiC	choroid plexus:	n/a
43	chr1:85156370-85156420	PFSK-1	brain:	n/a
44	chr1:85156430-85156480	HUVEC	blood vessel:	n/a
45	chr1:85156797-85156847	Hepatocyte	liver:	n/a
46	chr1:85156266-85156316	CMK	blood:	n/a
47	chr1:85156638-85156688	PrEC	prostate:	n/a
48	chr1:85156326-85156376	ovcar-3	ovarian:	n/a
49	chr1:85156370-85156420	HIPEpiC	eye:	n/a
50	chr1:85157327-85157377	BE2_C	brain:	n/a

(count:14 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:85038587..85040484-chr1:85154316..85157145,3	K562	blood:
2	chr1:85155931..85156464-chr19:1268879..1269406,2	Hela-S3	cervix:
3	chr1:84970994..84973830-chr1:85154472..85157447,5	K562	blood:
4	chr1:85156633..85159408-chr1:85174909..85176958,2	MCF-7	breast:
5	chr1:85155836..85156616-chr9:34611353..34612328,2	NB4	blood:
6	chr1:78469181..78471632-chr1:85154975..85157700,2	K562	blood:
7	chr1:85152648..85155097-chr1:85155098..85157489,2	MCF-7	breast:
8	chr1:84969596..84972494-chr1:85154864..85156849,3	K562	blood:
9	chr1:85157179..85159526-chr1:85171730..85173430,2	K562	blood:
10	chr1:85153044..85155913-chr1:85168206..85170903,2	K562	blood:
11	chr1:85038984..85041113-chr1:85155645..85157338,2	K562	blood:
12	chr1:85155689..85156552-chr1:95392412..95393058,2	HCT-116	colon:
13	chr1:84542242..84543745-chr1:85154770..85157524,2	K562	blood:
14	chr1:85150908..85155231-chr1:85184814..85188587,5	K562	blood:

No data

Variant related genes	Relation type
SSX2IP	TF binding region
SSX2IP	CpG island
ENSG00000117155	chromatin interactions
ENSG00000117151	chromatin interactions
ENSG00000273338	chromatin interactions
ENSG00000117519	chromatin interactions
ENSG00000099622	chromatin interactions
ENSG00000162616	chromatin interactions
ENSG00000271576	chromatin interactions
ENSG00000122432	chromatin interactions
ENSG00000174021	chromatin interactions
ENSG00000164967	chromatin interactions

Extended variants
information (count: 97 )
Associated
traits (count: 95 )

Variant overlapped rSNPs/rCNVs (count:97 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs574718164	chr1:85154854-85154855	Active TSS Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
2	rs186843828	chr1:85154945-85154946	Active TSS Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
3	rs560757816	chr1:85154961-85154962	Active TSS Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
4	rs577658132	chr1:85155005-85155006	Active TSS Weak transcription Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
5	rs74098441	chr1:85155124-85155125	Active TSS Weak transcription Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh	Chromatin interactive region	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs367570062	chr1:85155136-85155137	Active TSS Weak transcription Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
7	rs531955866	chr1:85155145-85155146	Active TSS Weak transcription Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
8	rs553484710	chr1:85155183-85155184	Active TSS Weak transcription Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
9	rs573379615	chr1:85155184-85155185	Active TSS Weak transcription Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
10	rs58745132	chr1:85155195-85155196	Active TSS Weak transcription Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
11	rs370583285	chr1:85155247-85155248	Active TSS Flanking Active TSS Enhancers Weak transcription Bivalent/Poised TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
12	rs74098442	chr1:85155257-85155258	Active TSS Flanking Active TSS Enhancers Weak transcription Bivalent/Poised TSS	Chromatin interactive region	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs191726534	chr1:85155318-85155319	Active TSS Flanking Active TSS Enhancers Weak transcription Bivalent/Poised TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
14	rs527282063	chr1:85155319-85155320	Active TSS Flanking Active TSS Enhancers Weak transcription Bivalent/Poised TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
15	rs547418350	chr1:85155339-85155340	Active TSS Flanking Active TSS Enhancers Weak transcription Bivalent/Poised TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
16	rs570119546	chr1:85155365-85155366	Active TSS Flanking Active TSS Enhancers Weak transcription Bivalent/Poised TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
17	rs12404958	chr1:85155382-85155383	Active TSS Flanking Active TSS Enhancers Weak transcription Bivalent/Poised TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
18	rs549677575	chr1:85155422-85155423	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Bivalent/Poised TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
19	rs3768237	chr1:85155473-85155474	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Bivalent/Poised TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
20	rs535665140	chr1:85155476-85155477	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Bivalent/Poised TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
21	rs554747403	chr1:85155486-85155487	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Bivalent/Poised TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
22	rs574915982	chr1:85155532-85155533	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Bivalent/Poised TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
23	rs562568406	chr1:85155543-85155544	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Bivalent/Poised TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
24	rs113605145	chr1:85155644-85155645	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
25	rs554162377	chr1:85155649-85155650	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
26	rs74098443	chr1:85155652-85155653	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	Chromatin interactive region	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs546492795	chr1:85155672-85155673	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
28	rs193232602	chr1:85155712-85155713	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
29	rs1538848	chr1:85155719-85155720	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	Chromatin interactive region	7 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs374839208	chr1:85155787-85155788	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
31	rs561628603	chr1:85155839-85155840	Active TSS Bivalent/Poised TSS Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
32	rs527335867	chr1:85155862-85155863	Active TSS Bivalent/Poised TSS Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
33	rs540740011	chr1:85155901-85155902	Active TSS Bivalent/Poised TSS Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
34	rs563707430	chr1:85155903-85155904	Active TSS Bivalent/Poised TSS Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
35	rs556727198	chr1:85155920-85155921	Active TSS Bivalent/Poised TSS Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
36	rs545648789	chr1:85155971-85155972	Active TSS Bivalent/Poised TSS Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
37	rs549640593	chr1:85156074-85156075	Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
38	rs569648319	chr1:85156128-85156129	Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
39	rs11543164	chr1:85156134-85156135	Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
40	rs529067277	chr1:85156168-85156169	Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
41	rs549206729	chr1:85156200-85156201	Active TSS Flanking Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
42	rs565738709	chr1:85156205-85156206	Active TSS Flanking Active TSS Enhancers Weak transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
43	rs534258909	chr1:85156244-85156245	Active TSS Flanking Active TSS Enhancers Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
44	rs554322195	chr1:85156263-85156264	Active TSS Flanking Active TSS Enhancers Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
45	rs570838884	chr1:85156347-85156348	Active TSS Flanking Active TSS Enhancers Weak transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
46	rs543430300	chr1:85156361-85156362	Active TSS Flanking Active TSS Enhancers Weak transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
47	rs539876876	chr1:85156391-85156392	Active TSS Flanking Active TSS Enhancers Weak transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
48	rs556886962	chr1:85156402-85156403	Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
49	rs556887848	chr1:85156436-85156437	Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
50	rs372865948	chr1:85156474-85156475	Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:95)

Disease	PMID	Source
Colorectal cancer	16272173	CNVD
Medulloblastoma	21979893	CNVD
Wilms tumour	21544195	CNVD
Coronary Disease	20032323	CNVD
Prostate cancer	21965145	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Stargardt''s disease	17277736	CNVD
Neuroblastoma	17897457	CNVD
Uveal melanoma	21693616	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	21484798	CNVD
Non-syndromic sensorineural hearing loss	22290220	CNVD
Liposarcoma	21253554	CNVD
Breast cancer	21264507	CNVD
Acute myeloid leukemia	16864856	CNVD
Astrocytoma	17387387	CNVD
Cancer	21499728	CNVD
Glioblastoma multiforme	17387387	CNVD
Oligodendroglial tumors	17285580	CNVD
Papillary thyroid carcinoma	21436994	CNVD
Neuroblastoma	17535989	CNVD
Pheochromocytoma	17535989	CNVD
Prostate cancer	16705090	CNVD
Astrocytoma	17934521	CNVD
Colorectal cancer	19359472	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Neuroblastoma	17533364	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Autism	22495311	CNVD
Non-small cell lung cancer	21385341	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Chordoma	21602918	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Melanoma	18172304	CNVD
Multiple myeloma	16461302	CNVD
Cancer	21129771	CNVD
Autosomal dominant nocturnal frontal lobe epilepsy	18472482	CNVD
Hirschsprung''s Disease	21712996	CNVD
Non-small cell lung cancer	20864512	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Thrombocytopenia-absent radius syndrome	21933853	CNVD
Psychiatric disorder	22848183	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	20409316	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Lung cancer	18438408	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17393978	CNVD
Cervical cancer	21062161	CNVD
Cancer	21183584	CNVD
Breast cancer	21785460	CNVD
Breast cancer	21364760	CNVD
Rett syndrome	21593744	CNVD
Prostate cancer	16573809	CNVD
Breast cancer	16608533	CNVD
Ovarian cancer	21720365	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Ewing''s sarcoma	17952124	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Cancer	22429812	CNVD
Non-muscle invasive bladder neoplasm	19445696	CNVD
Breast cancer	17133270	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
small cell lung cancer	20016488	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Multiple myeloma	17550852	CNVD
Myelofibrosis	22110671	CNVD
Neuroblastoma	21899760	CNVD
Breast cancer	16397240	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Cancer	17440070	CNVD

Chromatin state (count:518 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:85106400-85155400	Weak transcription	Sigmoid Colon	Sigmoid Colon
2	chr1:85108000-85155000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
3	chr1:85126400-85155200	Weak transcription	Left Ventricle	heart
4	chr1:85138800-85155000	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
5	chr1:85152000-85155000	Active TSS	Brain Angular Gyrus	brain
6	chr1:85152600-85156800	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
7	chr1:85152800-85155200	Enhancers	Primary T killer naive cells fromperipheralblood	blood
8	chr1:85153000-85155000	Enhancers	Primary T helper naive cells fromperipheralblood	blood
9	chr1:85153200-85155000	Enhancers	Primary T helper cells PMA-I stimulated	--
10	chr1:85153200-85155200	Enhancers	Monocytes-CD14+_RO01746	blood
11	chr1:85153400-85155000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
12	chr1:85153600-85155000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
13	chr1:85153600-85155000	Enhancers	Fetal Heart	heart
14	chr1:85153600-85155200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
15	chr1:85153600-85157000	Active TSS	K562	blood
16	chr1:85153600-85157400	Active TSS	Stomach Smooth Muscle	stomach
17	chr1:85154000-85155000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
18	chr1:85154000-85155000	Enhancers	HSMM	muscle
19	chr1:85154000-85155200	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
20	chr1:85154000-85155600	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
21	chr1:85154000-85156800	Active TSS	GM12878-XiMat	blood
22	chr1:85154200-85155000	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
23	chr1:85154200-85155000	Enhancers	Primary T killer memory cells from peripheral blood	blood
24	chr1:85154200-85155200	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
25	chr1:85154200-85155200	Enhancers	Primary T helper naive cells from peripheral blood	blood
26	chr1:85154200-85155400	Enhancers	Primary monocytes fromperipheralblood	blood
27	chr1:85154200-85155400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
28	chr1:85154200-85155400	Flanking Active TSS	Thymus	Thymus
29	chr1:85154200-85155400	Flanking Active TSS	NHEK	skin
30	chr1:85154200-85155600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
31	chr1:85154400-85155000	Flanking Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
32	chr1:85154400-85155000	Enhancers	Breast Myoepithelial Primary Cells	Breast
33	chr1:85154400-85155000	Enhancers	Primary hematopoietic stem cells	blood
34	chr1:85154400-85155000	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
35	chr1:85154400-85155000	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
36	chr1:85154400-85155000	Enhancers	Brain Germinal Matrix	brain
37	chr1:85154400-85155000	Enhancers	Brain Substantia Nigra	brain
38	chr1:85154400-85155000	Enhancers	Fetal Stomach	stomach
39	chr1:85154400-85155000	Enhancers	Rectal Mucosa Donor 31	rectum
40	chr1:85154400-85155000	Enhancers	Stomach Mucosa	stomach
41	chr1:85154400-85155200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
42	chr1:85154400-85155200	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
43	chr1:85154400-85155200	Flanking Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
44	chr1:85154400-85155200	Flanking Active TSS	iPS-15b Cell Line	embryonic stem cell
45	chr1:85154400-85155200	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
46	chr1:85154400-85155200	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
47	chr1:85154400-85155200	Flanking Active TSS	Hela-S3	cervix
48	chr1:85154400-85155400	Enhancers	Primary neutrophils fromperipheralblood	blood
49	chr1:85154400-85155400	Flanking Active TSS	Fetal Kidney	kidney
50	chr1:85154400-85155400	Weak transcription	Small Intestine	intestine

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