Variant report

Variant	nsv566197
Chromosome Location	chr14:105780507-105784680
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:366)
CpG islands
(count:610)
Chromatin interactive
region (count:7)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:366 , 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	ATF3	chr14:105780701-105780901	K562	blood:	n/a	n/a
2	BHLHE40	chr14:105780749-105780943	GM12878	blood:	n/a	n/a
3	CCNT2	chr14:105780628-105781015	K562	blood:	n/a	n/a
4	CEBPB	chr14:105781963-105781971	K562	blood:	n/a	n/a
5	CEBPD	chr14:105780640-105780906	HepG2	liver:	n/a	n/a
6	CHD2	chr14:105780643-105780936	GM12878	blood:	n/a	n/a
7	CHD2	chr14:105780621-105781022	Hela-S3	cervix:	n/a	n/a
8	CREB1	chr14:105780630-105781137	A549	lung:	n/a	n/a
9	CREB1	chr14:105781217-105781485	A549	lung:	n/a	n/a
10	CREB1	chr14:105780289-105781183	HepG2	liver:	n/a	n/a
11	CTCF	chr14:105784060-105784210	HMF	breast:	n/a	n/a
12	CTCF	chr14:105784040-105784190	AG09319	gingival:	n/a	n/a
13	CTCF	chr14:105780420-105780570	GM12872	blood:	n/a	n/a
14	CTCF	chr14:105781699-105782031	GM12891	blood:	n/a	chr14:105781945-105781958
15	CTCF	chr14:105784000-105784150	AG04450	lung:	n/a	n/a
16	CTCF	chr14:105780480-105780630	GM12867	blood:	n/a	n/a
17	CTCF	chr14:105781702-105781875	GM12892	blood:	n/a	n/a
18	CTCF	chr14:105781660-105781810	GM12874	blood:	n/a	n/a
19	CTCF	chr14:105784090-105784144	GM12891	blood:	n/a	n/a
20	CTCF	chr14:105784000-105784150	AG10803	skin:	n/a	n/a
21	CTCF	chr14:105781738-105781819	Spleen_OC	spleen:	n/a	n/a
22	CTCF	chr14:105784040-105784190	HepG2	liver:	n/a	n/a
23	CTCF	chr14:105784020-105784170	HAc	cerebellar:	n/a	n/a
24	CTCF	chr14:105784020-105784170	HEEpiC	esophagus:	n/a	n/a
25	CTCF	chr14:105784020-105784170	HPF	lung:	n/a	n/a
26	CTCF	chr14:105780341-105780524	GM12892	blood:	n/a	n/a
27	CTCF	chr14:105784020-105784170	HMF	breast:	n/a	n/a
28	CTCF	chr14:105781700-105781850	SK-N-SH_RA	brain:	n/a	n/a
29	CTCF	chr14:105783960-105784110	HCFaa	heart:	n/a	n/a
30	CTCF	chr14:105784040-105784190	NHEK	skin:	n/a	n/a
31	CTCF	chr14:105781887-105781965	NHEK	skin:	n/a	chr14:105781945-105781958
32	CTCF	chr14:105781983-105782041	Spleen_OC	spleen:	n/a	n/a
33	CTCF	chr14:105781712-105781865	GM19238	blood:	n/a	n/a
34	CTCF	chr14:105781720-105781745	H1-hESC	embryonic stem cell:	n/a	n/a
35	CTCF	chr14:105781845-105781973	MCF-7	breast:	n/a	chr14:105781945-105781958
36	CTCF	chr14:105784000-105784150	HPAF	blood vessel:	n/a	n/a
37	CTCF	chr14:105784040-105784190	BJ	skin:	n/a	n/a
38	CTCF	chr14:105784000-105784150	SAEC	small airway:	n/a	n/a
39	CTCF	chr14:105781720-105781870	GM12864	blood:	n/a	n/a
40	CTCF	chr14:105781868-105781989	MCF-7	breast:	n/a	chr14:105781945-105781958
41	CTCF	chr14:105780360-105780510	GM12869	blood:	n/a	n/a
42	CTCF	chr14:105783980-105784130	NHDF-neo	bronchial:	n/a	n/a
43	CTCF	chr14:105784000-105784150	BJ	skin:	n/a	n/a
44	CTCF	chr14:105784079-105784115	ProgFib	skin:	n/a	n/a
45	CTCF	chr14:105781707-105781983	MCF-7	breast:	n/a	chr14:105781945-105781958
46	CTCF	chr14:105783880-105784030	HFF	foreskin:	n/a	n/a
47	CTCF	chr14:105781802-105781814	GM12878	blood:	n/a	n/a
48	CTCF	chr14:105781900-105782050	SAEC	small airway:	n/a	chr14:105781945-105781958
49	CTCF	chr14:105784000-105784150	AG09319	gingival:	n/a	n/a
50	CTCF	chr14:105781765-105781827	GM19240	blood:	n/a	n/a

(count:610 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:105784090-105784140	NHBE	bronchial:	n/a
2	chr14:105781308-105781358	Jurkat	blood:	n/a
3	chr14:105781366-105781416	IMR90	lung:	fetal
4	chr14:105781366-105781416	NH-A	brain:	n/a
5	chr14:105782817-105782867	RPTEC	kidney:	n/a
6	chr14:105783536-105783586	NHBE	bronchial:	n/a
7	chr14:105781946-105781996	SK-N-SH	brain:	n/a
8	chr14:105781308-105781358	HUVEC	blood vessel:	n/a
9	chr14:105781312-105781362	NHDF-neo	bronchial:	n/a
10	chr14:105781366-105781416	SK-N-SH_RA	brain:	n/a
11	chr14:105781946-105781996	NB4	blood:	n/a
12	chr14:105783687-105783737	MCF-7	breast:	n/a
13	chr14:105781366-105781416	H1-hESC	embryonic stem cell:	embryo
14	chr14:105784090-105784140	Hepatocyte	liver:	n/a
15	chr14:105783687-105783737	HCPEpiC	choroid plexus:	n/a
16	chr14:105781946-105781996	IMR90	lung:	fetal
17	chr14:105781312-105781362	ECC-1	luminal epithelium:	n/a
18	chr14:105784090-105784140	HNPCEpiC	eye:	n/a
19	chr14:105783627-105783677	Caco-2	colon:	n/a
20	chr14:105781366-105781416	HRPEpiC	eye:	n/a
21	chr14:105780695-105780745	BJ	skin:	n/a
22	chr14:105782817-105782867	PANC-1	pancreas:	n/a
23	chr14:105780695-105780745	HCF	heart:	n/a
24	chr14:105781366-105781416	PFSK-1	brain:	n/a
25	chr14:105783687-105783737	SAEC	small airway:	n/a
26	chr14:105783687-105783737	RPTEC	kidney:	n/a
27	chr14:105783687-105783737	AG04450	lung:	fetal
28	chr14:105781366-105781416	BJ	skin:	n/a
29	chr14:105783687-105783737	U87	brain:	n/a
30	chr14:105783627-105783677	A549	lung:	n/a
31	chr14:105781312-105781362	Caco-2	colon:	n/a
32	chr14:105784090-105784140	AG10803	skin:	n/a
33	chr14:105781946-105781996	HAEpiC	amniotic membrane:	n/a
34	chr14:105781308-105781358	IMR90	lung:	fetal
35	chr14:105783536-105783586	PANC-1	pancreas:	n/a
36	chr14:105782817-105782867	SK-N-SH	brain:	n/a
37	chr14:105780695-105780745	K562	blood:	n/a
38	chr14:105781308-105781358	HCF	heart:	n/a
39	chr14:105781312-105781362	HEK293	kidney:	embryo
40	chr14:105784090-105784140	GM12892	blood:	n/a
41	chr14:105782817-105782867	Jurkat	blood:	n/a
42	chr14:105781312-105781362	BJ	skin:	n/a
43	chr14:105780695-105780745	Caco-2	colon:	n/a
44	chr14:105783687-105783737	AG09319	gingival:	n/a
45	chr14:105781366-105781416	AG09309	skin:	n/a
46	chr14:105781308-105781358	A549	lung:	n/a
47	chr14:105783627-105783677	ovcar-3	ovarian:	n/a
48	chr14:105781946-105781996	Hela-S3	cervix:	n/a
49	chr14:105783687-105783737	PFSK-1	brain:	n/a
50	chr14:105783627-105783677	SK-N-MC	brain:	n/a

(count:7 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr14:105779526..105781902-chr14:105955293..105957927,2	MCF-7	breast:
2	chr14:105765307..105769571-chr14:105774220..105784135,13	K562	blood:
3	chr14:105778405..105782273-chr14:105864844..105868439,3	K562	blood:
4	chr14:105765282..105769482-chr14:105778355..105784135,18	K562	blood:
5	chr14:105647226..105648734-chr14:105780236..105782314,2	MCF-7	breast:
6	chr14:105647019..105649589-chr14:105780411..105782070,2	MCF-7	breast:
7	chr14:105778878..105784143-chr14:105784229..105795178,22	MCF-7	breast:

No data

Variant related genes	Relation type
BRF1	TF binding region
PACS2	TF binding region
BRF1	CpG island
PACS2	CpG island
ENSG00000257622	chromatin interactions
ENSG00000183828	chromatin interactions
ENSG00000185024	chromatin interactions
ENSG00000179364	chromatin interactions
ENSG00000226174	chromatin interactions
ENSG00000185347	chromatin interactions

Extended variants
information (count: 132 )
Associated
traits (count: 106 )

Variant overlapped rSNPs/rCNVs (count:132 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs368620678	chr14:105780514-105780515	Active TSS Flanking Active TSS Bivalent/Poised TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
2	rs113540988	chr14:105780544-105780545	Active TSS Flanking Active TSS Bivalent/Poised TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
3	rs192761952	chr14:105780564-105780565	Active TSS Flanking Active TSS Bivalent/Poised TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
4	rs587627808	chr14:105780616-105780617	Weak transcription Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
5	rs144325169	chr14:105780654-105780655	Weak transcription Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
6	rs587740748	chr14:105780800-105780801	Weak transcription Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
7	rs587611670	chr14:105780801-105780802	Weak transcription Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
8	rs587618288	chr14:105780804-105780805	Weak transcription Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
9	rs587695943	chr14:105780873-105780874	Weak transcription Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
10	rs587751332	chr14:105781256-105781257	Weak transcription Active TSS Bivalent/Poised TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
11	rs587613193	chr14:105781257-105781258	Weak transcription Active TSS Bivalent/Poised TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
12	rs587698346	chr14:105781288-105781289	Weak transcription Active TSS Bivalent/Poised TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
13	rs587752605	chr14:105781412-105781413	Weak transcription Active TSS Bivalent/Poised TSS Flanking Active TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
14	rs587675129	chr14:105781450-105781451	Weak transcription Active TSS Bivalent/Poised TSS Flanking Active TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
15	rs183686378	chr14:105781562-105781563	Weak transcription Active TSS Bivalent/Poised TSS Flanking Active TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
16	rs188351899	chr14:105781735-105781736	Bivalent/Poised TSS Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription Flanking Bivalent TSS/Enh	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
17	rs181795615	chr14:105781780-105781781	Bivalent/Poised TSS Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription Flanking Bivalent TSS/Enh	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
18	rs587746155	chr14:105781887-105781888	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
19	rs375484605	chr14:105781900-105781901	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
20	rs587594311	chr14:105781915-105781916	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
21	rs587663661	chr14:105781938-105781939	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
22	rs587704862	chr14:105781941-105781942	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
23	rs146576316	chr14:105781961-105781962	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
24	rs587663156	chr14:105781999-105782000	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
25	rs587741159	chr14:105782010-105782011	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
26	rs587618349	chr14:105782011-105782012	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
27	rs369553680	chr14:105782015-105782016	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
28	rs587675341	chr14:105782083-105782084	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
29	rs587738576	chr14:105782112-105782113	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
30	rs371924110	chr14:105782140-105782141	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
31	rs587695320	chr14:105782163-105782164	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
32	rs587733301	chr14:105782178-105782179	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
33	rs587654016	chr14:105782182-105782183	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
34	rs113896520	chr14:105782185-105782186	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
35	rs587776172	chr14:105782192-105782193	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
36	rs190571012	chr14:105782229-105782230	Bivalent/Poised TSS Active TSS Flanking Active TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
37	rs587692412	chr14:105782237-105782238	Bivalent/Poised TSS Active TSS Flanking Active TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
38	rs587744439	chr14:105782243-105782244	Bivalent/Poised TSS Active TSS Flanking Active TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
39	rs587650220	chr14:105782286-105782287	Bivalent/Poised TSS Active TSS Flanking Active TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
40	rs587699591	chr14:105782377-105782378	Bivalent/Poised TSS Active TSS Flanking Active TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs368663980	chr14:105782388-105782389	Bivalent/Poised TSS Active TSS Flanking Active TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs587607493	chr14:105782391-105782392	Bivalent/Poised TSS Active TSS Flanking Active TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs587640961	chr14:105782464-105782465	Bivalent/Poised TSS Enhancers Flanking Active TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs141260195	chr14:105782465-105782466	Bivalent/Poised TSS Enhancers Flanking Active TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs61996226	chr14:105782503-105782504	Bivalent/Poised TSS Enhancers Flanking Active TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs587609782	chr14:105782521-105782522	Bivalent/Poised TSS Enhancers Flanking Active TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs181792551	chr14:105782527-105782528	Bivalent/Poised TSS Enhancers Flanking Active TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs587745555	chr14:105782537-105782538	Bivalent/Poised TSS Enhancers Flanking Active TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs587598455	chr14:105782547-105782548	Bivalent/Poised TSS Enhancers Flanking Active TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs35669521	chr14:105782570-105782571	Bivalent/Poised TSS Enhancers Flanking Active TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:106)

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
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	18451855	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

Chromatin state (count:619 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:105779200-105780600	Flanking Active TSS	Stomach Smooth Muscle	stomach
2	chr14:105779400-105780600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
3	chr14:105779400-105780600	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
4	chr14:105779400-105780600	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
5	chr14:105779400-105780600	Enhancers	Spleen	Spleen
6	chr14:105779600-105780600	Flanking Active TSS	Brain Germinal Matrix	brain
7	chr14:105779600-105780600	Flanking Active TSS	Colonic Mucosa	Colon
8	chr14:105779600-105780600	Enhancers	Fetal Brain Male	brain
9	chr14:105779800-105780600	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
10	chr14:105779800-105780800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
11	chr14:105779800-105780800	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
12	chr14:105779800-105782400	Active TSS	Fetal Kidney	kidney
13	chr14:105780000-105780600	Flanking Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
14	chr14:105780000-105780600	Flanking Active TSS	Primary T helper naive cells fromperipheralblood	blood
15	chr14:105780000-105780600	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
16	chr14:105780000-105780600	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
17	chr14:105780000-105780600	Flanking Active TSS	Fetal Brain Female	brain
18	chr14:105780000-105780600	Flanking Active TSS	Dnd41	blood
19	chr14:105780000-105781800	Active TSS	iPS-20b Cell Line	embryonic stem cell
20	chr14:105780000-105782800	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
21	chr14:105780200-105780600	Active TSS	ES-WA7 Cell Line	embryonic stem cell
22	chr14:105780200-105780600	Flanking Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
23	chr14:105780200-105780600	Flanking Active TSS	Primary B cells from cord blood	blood
24	chr14:105780200-105780600	Flanking Active TSS	Primary T cells fromperipheralblood	blood
25	chr14:105780200-105780600	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
26	chr14:105780200-105780600	Flanking Active TSS	Primary T helper 17 cells PMA-I stimulated	--
27	chr14:105780200-105780600	Flanking Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
28	chr14:105780200-105780600	Flanking Active TSS	Primary Natural Killer cells fromperipheralblood	blood
29	chr14:105780200-105780600	Flanking Active TSS	Cortex derived primary cultured neurospheres	brain
30	chr14:105780200-105780600	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
31	chr14:105780200-105780600	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
32	chr14:105780200-105780600	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
33	chr14:105780200-105780600	Flanking Active TSS	Fetal Adrenal Gland	Adrenal Gland
34	chr14:105780200-105780600	Flanking Active TSS	Fetal Muscle Trunk	muscle
35	chr14:105780200-105780600	Flanking Active TSS	Fetal Thymus	thymus
36	chr14:105780200-105780600	Flanking Active TSS	HMEC	breast
37	chr14:105780200-105780800	Flanking Active TSS	Primary hematopoietic stem cells	blood
38	chr14:105780200-105781600	Active TSS	HUES64 Cell Line	embryonic stem cell
39	chr14:105780200-105781800	Active TSS	iPS-18 Cell Line	embryonic stem cell
40	chr14:105780200-105781800	Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
41	chr14:105780200-105781800	Active TSS	K562	blood
42	chr14:105780200-105782000	Active TSS	iPS-15b Cell Line	embryonic stem cell
43	chr14:105780200-105782000	Active TSS	Breast Myoepithelial Primary Cells	Breast
44	chr14:105780200-105782000	Active TSS	Left Ventricle	heart
45	chr14:105780200-105782000	Active TSS	Hela-S3	cervix
46	chr14:105780200-105782200	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
47	chr14:105780200-105782200	Active TSS	Ovary	ovary
48	chr14:105780200-105782200	Active TSS	Right Atrium	heart
49	chr14:105780200-105782200	Active TSS	HepG2	liver
50	chr14:105780200-105782400	Active TSS	H9 Cell Line	embryonic stem cell

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