Variant report

Variant	esv1821473
Chromosome Location	chr14:105779305-105784680
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:398)
CpG islands
(count:1161)
Chromatin interactive
region (count:7)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:398 , 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	CHD2	chr14:105780426-105780462	H1-hESC	embryonic stem cell:	n/a	n/a
9	CREB1	chr14:105780289-105781183	HepG2	liver:	n/a	n/a
10	CREB1	chr14:105780630-105781137	A549	lung:	n/a	n/a
11	CREB1	chr14:105781217-105781485	A549	lung:	n/a	n/a
12	CTCF	chr14:105780240-105780390	AG10803	skin:	n/a	n/a
13	CTCF	chr14:105784000-105784150	AG04450	lung:	n/a	n/a
14	CTCF	chr14:105784000-105784150	AG09319	gingival:	n/a	n/a
15	CTCF	chr14:105784060-105784210	HMF	breast:	n/a	n/a
16	CTCF	chr14:105783980-105784130	NHDF-neo	bronchial:	n/a	n/a
17	CTCF	chr14:105784040-105784190	HepG2	liver:	n/a	n/a
18	CTCF	chr14:105781900-105782050	SAEC	small airway:	n/a	chr14:105781945-105781958
19	CTCF	chr14:105781720-105781870	GM12864	blood:	n/a	n/a
20	CTCF	chr14:105781800-105781950	GM12875	blood:	n/a	n/a
21	CTCF	chr14:105783980-105784130	HCPEpiC	choroid plexus:	n/a	n/a
22	CTCF	chr14:105784200-105784350	GM06990	blood:	n/a	n/a
23	CTCF	chr14:105781720-105781870	GM12873	blood:	n/a	n/a
24	CTCF	chr14:105783920-105784190	NHEK	skin:	n/a	n/a
25	CTCF	chr14:105780474-105780478	GM19240	blood:	n/a	n/a
26	CTCF	chr14:105781712-105781865	GM19238	blood:	n/a	n/a
27	CTCF	chr14:105781707-105781983	MCF-7	breast:	n/a	chr14:105781945-105781958
28	CTCF	chr14:105784020-105784170	HEEpiC	esophagus:	n/a	n/a
29	CTCF	chr14:105780440-105780590	HMEC	breast:	n/a	n/a
30	CTCF	chr14:105781868-105781989	MCF-7	breast:	n/a	chr14:105781945-105781958
31	CTCF	chr14:105780482-105780493	GM19240	blood:	n/a	n/a
32	CTCF	chr14:105784060-105784210	AG04450	lung:	n/a	n/a
33	CTCF	chr14:105780320-105780470	SK-N-SH_RA	brain:	n/a	n/a
34	CTCF	chr14:105780380-105780530	AG04449	skin:	n/a	n/a
35	CTCF	chr14:105781660-105781810	GM12874	blood:	n/a	n/a
36	CTCF	chr14:105781700-105781850	AG04449	skin:	n/a	n/a
37	CTCF	chr14:105784020-105784170	HMF	breast:	n/a	n/a
38	CTCF	chr14:105780340-105780490	GM12864	blood:	n/a	n/a
39	CTCF	chr14:105781983-105782041	Spleen_OC	spleen:	n/a	n/a
40	CTCF	chr14:105783960-105784110	RPTEC	kidney:	n/a	n/a
41	CTCF	chr14:105780340-105780490	GM12871	blood:	n/a	n/a
42	CTCF	chr14:105780341-105780524	GM12892	blood:	n/a	n/a
43	CTCF	chr14:105781764-105781769	Fibrobl	skin:	n/a	n/a
44	CTCF	chr14:105781845-105781973	MCF-7	breast:	n/a	chr14:105781945-105781958
45	CTCF	chr14:105780360-105780510	GM12873	blood:	n/a	n/a
46	CTCF	chr14:105780280-105780430	GM12878	blood:	n/a	n/a
47	CTCF	chr14:105784040-105784190	AoAF	blood vessel:	n/a	n/a
48	CTCF	chr14:105783960-105784110	HCFaa	heart:	n/a	n/a
49	CTCF	chr14:105781887-105781965	NHEK	skin:	n/a	chr14:105781945-105781958
50	CTCF	chr14:105783980-105784130	HMEC	breast:	n/a	n/a

(count:1161 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:105780431-105780481	K562	blood:	n/a
2	chr14:105781308-105781358	U87	brain:	n/a
3	chr14:105780431-105780481	K562	blood:	n/a
4	chr14:105781308-105781358	U87	brain:	n/a
5	chr14:105781366-105781416	HCPEpiC	choroid plexus:	n/a
6	chr14:105779910-105779960	SKMC	muscle:	n/a
7	chr14:105783687-105783737	HCT-116	colon:	n/a
8	chr14:105783536-105783586	K562	blood:	n/a
9	chr14:105781308-105781358	NB4	blood:	n/a
10	chr14:105784090-105784140	RPTEC	kidney:	n/a
11	chr14:105783536-105783586	AoSMC	blood vessel:	n/a
12	chr14:105783536-105783586	Hela-S3	cervix:	n/a
13	chr14:105779952-105780002	NHDF-neo	bronchial:	n/a
14	chr14:105779826-105779876	NHBE	bronchial:	n/a
15	chr14:105779794-105779844	H1-hESC	embryonic stem cell:	embryo
16	chr14:105779532-105779582	LNCaP	prostate:	n/a
17	chr14:105781312-105781362	ProgFib	skin:	n/a
18	chr14:105781312-105781362	NB4	blood:	n/a
19	chr14:105781312-105781362	HEEpiC	esophagus:	n/a
20	chr14:105782817-105782867	Caco-2	colon:	n/a
21	chr14:105780695-105780745	HRPEpiC	eye:	n/a
22	chr14:105779952-105780002	SAEC	small airway:	n/a
23	chr14:105781366-105781416	K562	blood:	n/a
24	chr14:105780340-105780390	SKMC	muscle:	n/a
25	chr14:105783536-105783586	AG04450	lung:	fetal
26	chr14:105780431-105780481	MCF-7	breast:	n/a
27	chr14:105781312-105781362	K562	blood:	n/a
28	chr14:105779826-105779876	GM12878	blood:	n/a
29	chr14:105781312-105781362	T-47D	breast:	n/a
30	chr14:105780695-105780745	HRE	kidney:	n/a
31	chr14:105780431-105780481	Hepatocyte	liver:	n/a
32	chr14:105783627-105783677	RPTEC	kidney:	n/a
33	chr14:105781366-105781416	MCF10A-Er-Src	breast:	n/a
34	chr14:105780340-105780390	GM12878	blood:	n/a
35	chr14:105780340-105780390	GM19239	blood:	n/a
36	chr14:105779952-105780002	HEEpiC	esophagus:	n/a
37	chr14:105780137-105780187	HL-60	blood:	n/a
38	chr14:105781946-105781996	HepG2	liver:	n/a
39	chr14:105780431-105780481	ProgFib	skin:	n/a
40	chr14:105781312-105781362	HepG2	liver:	n/a
41	chr14:105780695-105780745	HMEC	breast:	n/a
42	chr14:105783536-105783586	HCM	heart:	n/a
43	chr14:105780137-105780187	U87	brain:	n/a
44	chr14:105781312-105781362	HPAEpiC	pulmonary alveolar:	n/a
45	chr14:105783687-105783737	A549	lung:	n/a
46	chr14:105783687-105783737	SAEC	small airway:	n/a
47	chr14:105780340-105780390	RPTEC	kidney:	n/a
48	chr14:105781312-105781362	NHBE	bronchial:	n/a
49	chr14:105784090-105784140	Jurkat	blood:	n/a
50	chr14:105780431-105780481	Caco-2	colon:	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	chr14:105765282..105769482-chr14:105778355..105784135,18	K562	blood:
3	chr14:105778405..105782273-chr14:105864844..105868439,3	K562	blood:
4	chr14:105778878..105784143-chr14:105784229..105795178,22	MCF-7	breast:
5	chr14:105647226..105648734-chr14:105780236..105782314,2	MCF-7	breast:
6	chr14:105765307..105769571-chr14:105774220..105784135,13	K562	blood:
7	chr14:105647019..105649589-chr14:105780411..105782070,2	MCF-7	breast:

No data

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

Extended variants
information (count: 167 )
Associated
traits (count: 106 )

Variant overlapped rSNPs/rCNVs (count:167 , 50 per page) page: 1 2 3 4

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11847295	chr14:105779305-105779306	Weak transcription Genic enhancers Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs587743225	chr14:105779310-105779311	Weak transcription Genic enhancers Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
3	rs148025879	chr14:105779336-105779337	Weak transcription Genic enhancers Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
4	rs587716383	chr14:105779347-105779348	Weak transcription Genic enhancers Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
5	rs143538133	chr14:105779394-105779395	Weak transcription Genic enhancers Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
6	rs193154199	chr14:105779415-105779416	Weak transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
7	rs147161847	chr14:105779433-105779434	Weak transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
8	rs587706520	chr14:105779441-105779442	Weak transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
9	rs185342349	chr14:105779463-105779464	Weak transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
10	rs587676138	chr14:105779535-105779536	Weak transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
11	rs587756088	chr14:105779550-105779551	Weak transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
12	rs116735128	chr14:105779551-105779552	Weak transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
13	rs587684862	chr14:105779577-105779578	Weak transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
14	rs188202047	chr14:105779609-105779610	Weak transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
15	rs587623882	chr14:105779630-105779631	Weak transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
16	rs140324261	chr14:105779631-105779632	Weak transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
17	rs587735307	chr14:105779644-105779645	Weak transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
18	rs144196917	chr14:105779659-105779660	Weak transcription Enhancers Genic enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
19	rs376903973	chr14:105779767-105779768	Weak transcription Enhancers Genic enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
20	rs150703123	chr14:105779794-105779795	Weak transcription Enhancers Genic enhancers Flanking Active TSS	CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
21	rs139995749	chr14:105779811-105779812	Weak transcription Enhancers Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Active TSS	CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
22	rs587614160	chr14:105779826-105779827	Weak transcription Enhancers Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Active TSS	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
23	rs201530963	chr14:105779848-105779849	Weak transcription Enhancers Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Active TSS	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
24	rs149839207	chr14:105779932-105779933	Weak transcription Enhancers Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Active TSS	CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
25	rs112243624	chr14:105779968-105779969	Weak transcription Enhancers Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Active TSS	CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
26	rs113722440	chr14:105779974-105779975	Weak transcription Enhancers Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Active TSS	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
27	rs587650475	chr14:105780001-105780002	Bivalent Enhancer Flanking Active TSS Enhancers Weak transcription Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
28	rs145821978	chr14:105780048-105780049	Bivalent Enhancer Flanking Active TSS Enhancers Weak transcription Active TSS Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
29	rs587755385	chr14:105780066-105780067	Bivalent Enhancer Flanking Active TSS Enhancers Weak transcription Active TSS Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
30	rs114638134	chr14:105780168-105780169	Bivalent Enhancer Flanking Active TSS Enhancers Weak transcription Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
31	rs34626097	chr14:105780292-105780293	Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
32	rs587731483	chr14:105780439-105780440	Active TSS Flanking Active TSS Bivalent/Poised TSS Weak transcription Enhancers	TF binding region CpG island Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
33	rs587627693	chr14:105780456-105780457	Active TSS Flanking Active TSS Bivalent/Poised TSS Weak transcription Enhancers	TF binding region CpG island Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
34	rs587688914	chr14:105780490-105780491	Active TSS Flanking Active TSS Bivalent/Poised TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
35	rs374452568	chr14:105780506-105780507	Active TSS Flanking Active TSS Bivalent/Poised TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
36	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
37	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
38	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
39	rs587627808	chr14:105780616-105780617	Weak transcription Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
40	rs144325169	chr14:105780654-105780655	Weak transcription Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
41	rs587740748	chr14:105780800-105780801	Weak transcription Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
42	rs587611670	chr14:105780801-105780802	Weak transcription Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
43	rs587618288	chr14:105780804-105780805	Weak transcription Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
44	rs587695943	chr14:105780873-105780874	Weak transcription Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
45	rs587751332	chr14:105781256-105781257	Weak transcription Active TSS Bivalent/Poised TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
46	rs587613193	chr14:105781257-105781258	Weak transcription Active TSS Bivalent/Poised TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
47	rs587698346	chr14:105781288-105781289	Weak transcription Active TSS Bivalent/Poised TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
48	rs587752605	chr14:105781412-105781413	Weak transcription Active TSS Bivalent/Poised TSS Flanking Active TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
49	rs587675129	chr14:105781450-105781451	Weak transcription Active TSS Bivalent/Poised TSS Flanking Active TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
50	rs183686378	chr14:105781562-105781563	Weak transcription Active TSS Bivalent/Poised TSS Flanking Active TSS	Chromatin interactive region	6 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:837 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:105768200-105779400	Weak transcription	Colonic Mucosa	Colon
2	chr14:105768200-105779400	Weak transcription	Thymus	Thymus
3	chr14:105768200-105779600	Weak transcription	GM12878-XiMat	blood
4	chr14:105768200-105779800	Weak transcription	NHLF	lung
5	chr14:105768200-105780000	Weak transcription	NHDF-Ad	bronchial
6	chr14:105768200-105780200	Weak transcription	Gastric	stomach
7	chr14:105768200-105780200	Weak transcription	Right Atrium	heart
8	chr14:105768400-105779400	Weak transcription	Skeletal Muscle Male	skeletal muscle
9	chr14:105768400-105779800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
10	chr14:105768400-105779800	Weak transcription	Lung	lung
11	chr14:105768400-105780200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
12	chr14:105770800-105779600	Weak transcription	Rectal Mucosa Donor 29	rectum
13	chr14:105771400-105780200	Weak transcription	Sigmoid Colon	Sigmoid Colon
14	chr14:105771600-105780000	Weak transcription	K562	blood
15	chr14:105772200-105779800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
16	chr14:105772200-105780000	Weak transcription	Primary T cells from cord blood	blood
17	chr14:105772400-105779400	Weak transcription	Spleen	Spleen
18	chr14:105772400-105779800	Weak transcription	Primary T cells fromperipheralblood	blood
19	chr14:105772400-105779800	Weak transcription	Primary T helper cells fromperipheralblood	blood
20	chr14:105772600-105779400	Weak transcription	Fetal Thymus	thymus
21	chr14:105773800-105779800	Weak transcription	Fetal Intestine Small	intestine
22	chr14:105774000-105779400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
23	chr14:105774200-105780000	Weak transcription	HUES48 Cell Line	embryonic stem cell
24	chr14:105774200-105780200	Weak transcription	H9 Cell Line	embryonic stem cell
25	chr14:105776000-105780000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
26	chr14:105776000-105780000	Weak transcription	NHEK	skin
27	chr14:105776200-105780000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
28	chr14:105776200-105780000	Weak transcription	HMEC	breast
29	chr14:105777400-105779800	Weak transcription	Dnd41	blood
30	chr14:105777600-105779600	Enhancers	Brain Hippocampus Middle	brain
31	chr14:105777600-105779800	Enhancers	Brain Cingulate Gyrus	brain
32	chr14:105777800-105779600	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
33	chr14:105778000-105779400	Enhancers	Brain Anterior Caudate	brain
34	chr14:105778000-105779400	Enhancers	Brain Inferior Temporal Lobe	brain
35	chr14:105778000-105779800	Enhancers	Brain Substantia Nigra	brain
36	chr14:105778000-105780200	Genic enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
37	chr14:105778000-105780200	Enhancers	Fetal Stomach	stomach
38	chr14:105778200-105779800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
39	chr14:105778200-105780000	Enhancers	Fetal Muscle Leg	muscle
40	chr14:105778200-105780200	Enhancers	Fetal Muscle Trunk	muscle
41	chr14:105778400-105779800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
42	chr14:105778400-105780200	Weak transcription	Right Ventricle	heart
43	chr14:105778600-105779400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
44	chr14:105778600-105779800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
45	chr14:105778600-105779800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
46	chr14:105778600-105779800	Weak transcription	Pancreas	Pancrea
47	chr14:105778600-105780000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
48	chr14:105778600-105780000	Enhancers	Brain Angular Gyrus	brain
49	chr14:105778600-105780200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
50	chr14:105778800-105779400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--

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