Variant report

Variant	nsv902468
Chromosome Location	chr14:105712091-105721808
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:379)
CpG islands
(count:1039)
Chromatin interactive
region (count:13)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:379 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr14:105714406-105715709	H1-hESC	embryonic stem cell:	n/a	n/a
2	BCLAF1	chr14:105714554-105714894	GM12878	blood:	n/a	chr14:105714818-105714831
3	BHLHE40	chr14:105714708-105714897	GM12878	blood:	n/a	chr14:105714722-105714738
4	BRCA1	chr14:105714311-105714507	H1-hESC	embryonic stem cell:	n/a	n/a
5	BRCA1	chr14:105714576-105714669	GM12878	blood:	n/a	n/a
6	CCNT2	chr14:105719576-105719641	K562	blood:	n/a	n/a
7	CEBPB	chr14:105711878-105712144	HepG2	liver:	n/a	chr14:105711997-105712008
8	CEBPB	chr14:105720824-105721085	Hela-S3	cervix:	n/a	n/a
9	CEBPB	chr14:105720892-105721012	K562	blood:	n/a	n/a
10	CEBPB	chr14:105720781-105721070	IMR90	lung:	n/a	n/a
11	CEBPB	chr14:105720811-105721087	A549	lung:	n/a	n/a
12	CHD1	chr14:105714496-105714696	GM12878	blood:	n/a	n/a
13	CHD2	chr14:105714688-105714896	Hela-S3	cervix:	n/a	chr14:105714767-105714777
14	CHD2	chr14:105714441-105714842	H1-hESC	embryonic stem cell:	n/a	chr14:105714767-105714777
15	CREB1	chr14:105714431-105715408	A549	lung:	n/a	n/a
16	CREB1	chr14:105714633-105714984	A549	lung:	n/a	n/a
17	CREB1	chr14:105714614-105715071	ECC-1	luminal epithelium:	n/a	n/a
18	CREB1	chr14:105714484-105715182	GM12878	blood:	n/a	n/a
19	CREB1	chr14:105714545-105715112	H1-hESC	embryonic stem cell:	n/a	n/a
20	CREB1	chr14:105714486-105715078	H1-hESC	embryonic stem cell:	n/a	n/a
21	CTCF	chr14:105714880-105715030	Hela-S3	cervix:	n/a	n/a
22	CTCF	chr14:105714974-105715078	Spleen_OC	spleen:	n/a	n/a
23	CTCF	chr14:105721740-105721890	HBMEC	blood vessel:	n/a	n/a
24	CTCF	chr14:105714640-105714790	GM12867	blood:	n/a	n/a
25	CTCF	chr14:105714950-105715007	Hela-S3	cervix:	n/a	n/a
26	CTCF	chr14:105714928-105715090	GM12892	blood:	n/a	n/a
27	CTCF	chr14:105715560-105715710	HCPEpiC	choroid plexus:	n/a	n/a
28	CTCF	chr14:105714900-105715050	GM12871	blood:	n/a	n/a
29	CTCF	chr14:105715393-105715408	GM10248	blood:	n/a	n/a
30	CTCF	chr14:105714940-105715090	HA-sp	spinal cord:	n/a	n/a
31	CTCF	chr14:105715480-105715630	GM12875	blood:	n/a	n/a
32	CTCF	chr14:105714939-105715086	GM19240	blood:	n/a	n/a
33	CTCF	chr14:105715360-105715510	SK-N-SH_RA	brain:	n/a	n/a
34	CTCF	chr14:105714920-105715070	GM12878	blood:	n/a	n/a
35	CTCF	chr14:105721780-105721847	MCF-7	breast:	n/a	n/a
36	CTCF	chr14:105714880-105715030	GM12871	blood:	n/a	n/a
37	CTCF	chr14:105714918-105715111	MCF-7	breast:	n/a	n/a
38	CTCF	chr14:105715392-105715423	Pancreas_OC	pancreas:	n/a	n/a
39	CTCF	chr14:105714782-105714866	LNCaP	prostate:	n/a	n/a
40	CTCF	chr14:105714956-105715086	GM19239	blood:	n/a	n/a
41	CTCF	chr14:105714867-105714993	SK-N-SH_RA	brain:	n/a	n/a
42	CTCF	chr14:105714900-105715050	GM12865	blood:	n/a	n/a
43	CTCF	chr14:105714940-105715090	NHEK	skin:	n/a	n/a
44	CTCF	chr14:105714991-105715066	Fibrobl	skin:	n/a	n/a
45	CTCF	chr14:105714860-105715010	GM12864	blood:	n/a	n/a
46	CTCF	chr14:105714940-105715090	HEK293	kidney:	n/a	n/a
47	CTCF	chr14:105714940-105715090	GM12865	blood:	n/a	n/a
48	CTCF	chr14:105714940-105715032	GM10248	blood:	n/a	n/a
49	CTCF	chr14:105715062-105715065	GM10266	blood:	n/a	n/a
50	CTCF	chr14:105714200-105714350	GM12873	blood:	n/a	n/a

(count:1039 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:105714404-105714454	IMR90	lung:	fetal
2	chr14:105714833-105714883	HMEC	breast:	n/a
3	chr14:105714404-105714454	IMR90	lung:	fetal
4	chr14:105714833-105714883	HMEC	breast:	n/a
5	chr14:105713866-105713916	NH-A	brain:	n/a
6	chr14:105715926-105715976	CMK	blood:	n/a
7	chr14:105718851-105718901	T-47D	breast:	n/a
8	chr14:105718851-105718901	AG04450	lung:	fetal
9	chr14:105713866-105713916	U87	brain:	n/a
10	chr14:105715741-105715791	H1-hESC	embryonic stem cell:	embryo
11	chr14:105715025-105715075	RPTEC	kidney:	n/a
12	chr14:105714846-105714896	LNCaP	prostate:	n/a
13	chr14:105714833-105714883	GM19239	blood:	n/a
14	chr14:105715025-105715075	NHDF-neo	bronchial:	n/a
15	chr14:105714400-105714450	Caco-2	colon:	n/a
16	chr14:105715025-105715075	K562	blood:	n/a
17	chr14:105714843-105714893	AG04449	skin:	fetal
18	chr14:105714400-105714450	HMEC	breast:	n/a
19	chr14:105715741-105715791	MCF-7	breast:	n/a
20	chr14:105715025-105715075	GM12892	blood:	n/a
21	chr14:105715025-105715075	GM19239	blood:	n/a
22	chr14:105718851-105718901	H1-hESC	embryonic stem cell:	embryo
23	chr14:105715025-105715075	HAEpiC	amniotic membrane:	n/a
24	chr14:105713866-105713916	Hepatocyte	liver:	n/a
25	chr14:105714843-105714893	Hela-S3	cervix:	n/a
26	chr14:105714404-105714454	PrEC	prostate:	n/a
27	chr14:105715926-105715976	SK-N-SH	brain:	n/a
28	chr14:105718851-105718901	HEEpiC	esophagus:	n/a
29	chr14:105715741-105715791	AoSMC	blood vessel:	n/a
30	chr14:105714589-105714639	Jurkat	blood:	n/a
31	chr14:105714153-105714203	H1-hESC	embryonic stem cell:	embryo
32	chr14:105713866-105713916	HIPEpiC	eye:	n/a
33	chr14:105715741-105715791	SK-N-SH	brain:	n/a
34	chr14:105714404-105714454	CMK	blood:	n/a
35	chr14:105715926-105715976	SK-N-SH_RA	brain:	n/a
36	chr14:105715741-105715791	NT2-D1	testis:	n/a
37	chr14:105714379-105714429	Caco-2	colon:	n/a
38	chr14:105715926-105715976	ProgFib	skin:	n/a
39	chr14:105715741-105715791	ProgFib	skin:	n/a
40	chr14:105714274-105714324	A549	lung:	n/a
41	chr14:105714404-105714454	ProgFib	skin:	n/a
42	chr14:105715741-105715791	U87	brain:	n/a
43	chr14:105713866-105713916	SAEC	small airway:	n/a
44	chr14:105715741-105715791	MCF10A-Er-Src	breast:	n/a
45	chr14:105716052-105716102	ECC-1	luminal epithelium:	n/a
46	chr14:105714404-105714454	LNCaP	prostate:	n/a
47	chr14:105718851-105718901	ovcar-3	ovarian:	n/a
48	chr14:105718851-105718901	MCF-7	breast:	n/a
49	chr14:105718851-105718901	HIPEpiC	eye:	n/a
50	chr14:105714274-105714324	AG09319	gingival:	n/a

(count:13 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr14:105717742..105719473-chr14:105729003..105731764,2	MCF-7	breast:
2	chr14:105718698..105721537-chr14:105739124..105741867,2	MCF-7	breast:
3	chr14:105721297..105724046-chr14:105725585..105727720,2	MCF-7	breast:
4	chr14:105713833..105716142-chr14:105716723..105718932,2	K562	blood:
5	chr14:105709578..105712149-chr14:105714194..105716568,3	MCF-7	breast:
6	chr11:62358871..62359665-chr14:105714579..105715245,2	Hela-S3	cervix:
7	chr14:105717555..105718335-chr3:138200943..138201661,2	MCF-7	breast:
8	chr14:105687326..105689962-chr14:105713390..105716265,3	MCF-7	breast:
9	chr14:105706521..105709177-chr14:105712711..105714374,2	MCF-7	breast:
10	chr14:105713379..105716522-chr14:105764463..105769159,4	MCF-7	breast:
11	chr14:105717901..105719933-chr14:105721820..105724297,3	MCF-7	breast:
12	chr14:105718161..105724247-chr14:105765636..105769156,6	MCF-7	breast:
13	chr14:105633069..105635536-chr14:105714407..105716304,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-BTBD6-2	chr14:105717014-105717436	NONHSAT040340

No data

Variant related genes	Relation type
BRF1	TF binding region
BTBD6	TF binding region
BRF1	CpG island
BTBD6	CpG island
ENSG00000185024	chromatin interactions
ENSG00000149016	chromatin interactions
ENSG00000184887	chromatin interactions
ENSG00000179364	chromatin interactions
ENSG00000255508	chromatin interactions
ENSG00000184916	chromatin interactions

Extended variants
information (count: 440 )
Associated
traits (count: 107 )

Variant overlapped rSNPs/rCNVs (count:440 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs8010223	chr14:105712091-105712092	Weak transcription Strong transcription ZNF genes & repeats Enhancers Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
2	rs587652772	chr14:105712097-105712098	Weak transcription Strong transcription ZNF genes & repeats Enhancers Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
3	rs187737837	chr14:105712100-105712101	Weak transcription Strong transcription ZNF genes & repeats Enhancers Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
4	rs191312633	chr14:105712102-105712103	Weak transcription Strong transcription ZNF genes & repeats Enhancers Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
5	rs587760858	chr14:105712153-105712154	Weak transcription Strong transcription ZNF genes & repeats Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs183066629	chr14:105712185-105712186	Weak transcription Strong transcription ZNF genes & repeats Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs79647077	chr14:105712251-105712252	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs587716033	chr14:105712259-105712260	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs117701419	chr14:105712316-105712317	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs146870758	chr14:105712328-105712329	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs587733847	chr14:105712331-105712332	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs187742938	chr14:105712333-105712334	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs587688999	chr14:105712335-105712336	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs139264059	chr14:105712351-105712352	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs587601699	chr14:105712366-105712367	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs587660583	chr14:105712411-105712412	Weak transcription Strong transcription Enhancers Active TSS Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs192653505	chr14:105712437-105712438	Weak transcription Strong transcription Enhancers Active TSS Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs375712224	chr14:105712469-105712470	Weak transcription Strong transcription Enhancers Active TSS Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs587616263	chr14:105712477-105712478	Weak transcription Strong transcription Enhancers Active TSS Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs2816652	chr14:105712493-105712494	Weak transcription Strong transcription Enhancers Active TSS Flanking Active TSS Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
21	rs143173019	chr14:105712494-105712495	Weak transcription Strong transcription Enhancers Active TSS Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs144748739	chr14:105712499-105712500	Weak transcription Strong transcription Enhancers Active TSS Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs35865531	chr14:105712557-105712558	Weak transcription Strong transcription Enhancers Active TSS Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs587681185	chr14:105712567-105712568	Weak transcription Strong transcription Enhancers Active TSS Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs587765662	chr14:105712630-105712631	Weak transcription Strong transcription Enhancers Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs587635386	chr14:105712664-105712665	Weak transcription Strong transcription Enhancers Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs587700330	chr14:105712675-105712676	Weak transcription Strong transcription Enhancers Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs587752680	chr14:105712699-105712700	Weak transcription Strong transcription Enhancers Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs2735823	chr14:105712733-105712734	Weak transcription Strong transcription Enhancers Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs2735822	chr14:105712734-105712735	Weak transcription Strong transcription Enhancers Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
31	rs185211223	chr14:105712739-105712740	Weak transcription Strong transcription Enhancers Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs587633373	chr14:105712741-105712742	Weak transcription Strong transcription Enhancers Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs2735821	chr14:105712745-105712746	Weak transcription Strong transcription Enhancers Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs587668709	chr14:105712763-105712764	Weak transcription Strong transcription Enhancers Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs587699476	chr14:105712780-105712781	Weak transcription Strong transcription Enhancers Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs148113337	chr14:105712829-105712830	Weak transcription Strong transcription Genic enhancers Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs587741236	chr14:105712841-105712842	Weak transcription Strong transcription Genic enhancers Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs2735820	chr14:105712856-105712857	Weak transcription Strong transcription Genic enhancers Enhancers Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
39	rs12889421	chr14:105712863-105712864	Weak transcription Strong transcription Genic enhancers Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs12889029	chr14:105712886-105712887	Weak transcription Strong transcription Genic enhancers Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs66737076	chr14:105712887-105712888	Weak transcription Strong transcription Genic enhancers Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs587675431	chr14:105712906-105712907	Weak transcription Strong transcription Genic enhancers Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs587732813	chr14:105712945-105712946	Weak transcription Strong transcription Genic enhancers Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs12889164	chr14:105712946-105712947	Weak transcription Strong transcription Genic enhancers Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs113556684	chr14:105712995-105712996	Weak transcription Strong transcription Genic enhancers Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs200577520	chr14:105713006-105713007	Weak transcription Strong transcription Genic enhancers Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs140000606	chr14:105713036-105713037	Weak transcription Strong transcription Genic enhancers Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs190087973	chr14:105713078-105713079	Weak transcription Strong transcription Genic enhancers Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs587621781	chr14:105713118-105713119	Weak transcription Strong transcription Genic enhancers Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs192850649	chr14:105713129-105713130	Weak transcription Strong transcription Genic enhancers Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:107)

Disease	PMID	Source
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Retinoblastoma	21504564	CNVD
High-proliferative meningiomas	17937814	CNVD
Non-small cell lung cancer	21044232	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Melanoma	18172304	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Medulloblastoma	21979893	CNVD
Oral cancer	21386901	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Hepatocellular carcinoma	22174799	CNVD
Neuroblastoma	19435921	CNVD
Colorectal cancer	19359472	CNVD
Breast cancer	17899364	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Renal cell carcinoma	21668985	CNVD
Chronic myeloid leukemia	20724749	CNVD
Wilms tumour	21544195	CNVD
Lung cancer	18438408	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Colorectal cancer	16774939	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Neuroblastoma	18923191	CNVD
Barrett''s syndrome	19417022	CNVD
cataract	16735990	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Developmental delay	21147756	CNVD
Cancer	20164920	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Biliary cancer	19435499	CNVD
Follicular lymphoma	20505157	CNVD
Acute lymphoblastic leukemia	20139093	CNVD
Hepatocellular carcinoma	16750200	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Glioblastoma multiforme	21922591	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Ovarian cancer	22174824	CNVD
Non-small cell lung cancer	18320023	CNVD
Melanoma	17363583	CNVD
Prostate cancer	18632612	CNVD
Congenital heart defect	22367666	CNVD
Developmental delay	22367666	CNVD
Genitourinary abnormalities	22367666	CNVD
Intellectual disability	22367666	CNVD
Microcephaly	22367666	CNVD
Muscularhypotonia	22367666	CNVD
Ocular coloboma	22367666	CNVD
Teratozoospermia	22367666	CNVD
Cervical cancer	21062161	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Breast cancer	21990379	CNVD
Breast cancer	16417655	CNVD
22q11 deletion syndrome	22511897	CNVD
Cancer	21129771	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	22286061	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Schizophrenia	21399695	CNVD
Intracranial ependymoma	16609018	CNVD
Lung adenocarcinoma	17086460	CNVD
Gastric adenocarcinoma	19115996	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
14q deletion syndrome	22511897	CNVD
Epilepsy	22083797	CNVD
Ovarian cancer	21720365	CNVD
Cancer	17440070	CNVD
Neurocytoma	17123091	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Central neurocytomas	17123091	CNVD
Acute lymphoblastic leukemia	17315016	CNVD
Lung cancer	17086460	CNVD
Mortal	21835882	CNVD
small cell lung cancer	17426248	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Schizophrenia	20967226	CNVD
early-passage human iPS cells	21368824	CNVD
Williams Syndrome	20824207	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Pancreatic cancer	17952125	CNVD
Schizophrenia	23813976	CNVD
lymphocytic leukemia	21291569	CNVD
Cancer	20164919	CNVD
small cell lung cancer	20016488	CNVD
Recurrent pregnancy loss	19789632	CNVD
Non-syndromic sensorineural hearing loss	17431168	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Breast cancer	20369283	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:1031 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:105668600-105714200	Weak transcription	HUVEC	blood vessel
2	chr14:105669800-105713800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
3	chr14:105672400-105713200	Weak transcription	Osteobl	bone
4	chr14:105673600-105713600	Weak transcription	Stomach Mucosa	stomach
5	chr14:105676800-105713800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
6	chr14:105679800-105714000	Weak transcription	NHDF-Ad	bronchial
7	chr14:105680600-105714000	Weak transcription	Psoas Muscle	Psoas
8	chr14:105681400-105714000	Weak transcription	HSMMtube	muscle
9	chr14:105681400-105714200	Weak transcription	HSMM	muscle
10	chr14:105687200-105714000	Weak transcription	Muscle Satellite Cultured Cells	--
11	chr14:105687400-105714200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
12	chr14:105688800-105713800	Weak transcription	NH-A	brain
13	chr14:105689800-105714000	Weak transcription	HUES6 Cell Line	embryonic stem cell
14	chr14:105690200-105713800	Weak transcription	NHEK	skin
15	chr14:105690400-105714000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
16	chr14:105690400-105721400	Weak transcription	K562	blood
17	chr14:105691600-105714000	Weak transcription	Primary hematopoietic stem cells	blood
18	chr14:105693000-105713600	Weak transcription	Rectal Smooth Muscle	rectum
19	chr14:105693200-105713400	Weak transcription	GM12878-XiMat	blood
20	chr14:105693200-105713400	Weak transcription	Hela-S3	cervix
21	chr14:105693200-105713800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
22	chr14:105693200-105714000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
23	chr14:105693400-105714000	Weak transcription	Primary neutrophils fromperipheralblood	blood
24	chr14:105693600-105713200	Weak transcription	Primary T helper cells fromperipheralblood	blood
25	chr14:105693600-105713800	Weak transcription	Colon Smooth Muscle	Colon
26	chr14:105694000-105714200	Weak transcription	Duodenum Smooth Muscle	Duodenum
27	chr14:105694200-105713600	Weak transcription	Primary T helper cells PMA-I stimulated	--
28	chr14:105694200-105714200	Weak transcription	Primary T cells from cord blood	blood
29	chr14:105703800-105714200	Weak transcription	HUES48 Cell Line	embryonic stem cell
30	chr14:105706200-105713200	Weak transcription	HUES64 Cell Line	embryonic stem cell
31	chr14:105707200-105713800	Weak transcription	Fetal Thymus	thymus
32	chr14:105707200-105714000	Strong transcription	Primary hematopoietic stem cells short term culture	blood
33	chr14:105707400-105713400	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
34	chr14:105707600-105714000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
35	chr14:105707800-105714000	Weak transcription	H1 Cell Line	embryonic stem cell
36	chr14:105708000-105713400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
37	chr14:105708200-105714000	Weak transcription	Placenta Amnion	Placenta Amnion
38	chr14:105708400-105712400	Weak transcription	Adipose Nuclei	Adipose
39	chr14:105708400-105713200	Weak transcription	NHLF	lung
40	chr14:105708400-105713400	Weak transcription	Stomach Smooth Muscle	stomach
41	chr14:105708400-105713600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
42	chr14:105708400-105713600	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
43	chr14:105708400-105713600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
44	chr14:105708400-105713800	Weak transcription	Rectal Mucosa Donor 29	rectum
45	chr14:105708400-105713800	Weak transcription	Right Ventricle	heart
46	chr14:105708400-105714000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
47	chr14:105708400-105714000	Weak transcription	Rectal Mucosa Donor 31	rectum
48	chr14:105708600-105712400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
49	chr14:105708600-105712600	Weak transcription	Primary T cells fromperipheralblood	blood
50	chr14:105708600-105712600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin

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