Variant report

Variant	esv3449126
Chromosome Location	chr14:37678250-37700597
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr14:37699852-37700129	K562	blood:	n/a	n/a
2	ARID3A	chr14:37699763-37700208	HepG2	liver:	n/a	n/a
3	CBX3	chr14:37694473-37694666	K562	blood:	n/a	n/a
4	CBX3	chr14:37694370-37694773	K562	blood:	n/a	n/a
5	CEBPB	chr14:37693071-37693428	MCF-7	breast:	n/a	n/a
6	CTCF	chr14:37699778-37700093	K562	blood:	n/a	chr14:37699980-37699996 chr14:37699981-37700002 chr14:37699982-37699995 chr14:37699982-37699995 chr14:37699979-37699997
7	CTCF	chr14:37699940-37700090	GM12875	blood:	n/a	chr14:37699980-37699996 chr14:37699981-37700002 chr14:37699982-37699995 chr14:37699982-37699995 chr14:37699979-37699997
8	CTCF	chr14:37683806-37684143	A549	lung:	n/a	n/a
9	CTCF	chr14:37699880-37700030	GM12866	blood:	n/a	chr14:37699980-37699996 chr14:37699981-37700002 chr14:37699982-37699995 chr14:37699982-37699995 chr14:37699979-37699997
10	CTCF	chr14:37699880-37700030	AG09309	skin:	n/a	chr14:37699980-37699996 chr14:37699981-37700002 chr14:37699982-37699995 chr14:37699982-37699995 chr14:37699979-37699997
11	CTCF	chr14:37699160-37699310	RPTEC	kidney:	n/a	n/a
12	CTCF	chr14:37699617-37699682	Medullo	brain:	n/a	n/a
13	CTCF	chr14:37699790-37700177	K562	blood:	n/a	chr14:37699980-37699996 chr14:37699981-37700002 chr14:37699982-37699995 chr14:37699982-37699995 chr14:37699979-37699997
14	CTCF	chr14:37699872-37700102	K562	blood:	n/a	chr14:37699980-37699996 chr14:37699981-37700002 chr14:37699982-37699995 chr14:37699982-37699995 chr14:37699979-37699997
15	CTCF	chr14:37699940-37700090	AoAF	blood vessel:	n/a	chr14:37699980-37699996 chr14:37699981-37700002 chr14:37699982-37699995 chr14:37699982-37699995 chr14:37699979-37699997
16	CTCF	chr14:37699914-37700088	MCF-7	breast:	n/a	chr14:37699980-37699996 chr14:37699981-37700002 chr14:37699982-37699995 chr14:37699982-37699995 chr14:37699979-37699997
17	CTCF	chr14:37699900-37700050	AG09319	gingival:	n/a	chr14:37699980-37699996 chr14:37699981-37700002 chr14:37699982-37699995 chr14:37699982-37699995 chr14:37699979-37699997
18	CTCF	chr14:37700000-37700150	A549	lung:	n/a	n/a
19	CTCF	chr14:37699920-37700070	HPAF	blood vessel:	n/a	chr14:37699980-37699996 chr14:37699981-37700002 chr14:37699982-37699995 chr14:37699982-37699995 chr14:37699979-37699997
20	CTCF	chr14:37683911-37684048	Gliobla	brain:	n/a	n/a
21	CTCF	chr14:37699717-37700207	MCF-7	breast:	n/a	chr14:37699980-37699996 chr14:37699981-37700002 chr14:37699982-37699995 chr14:37699982-37699995 chr14:37699979-37699997
22	CTCF	chr14:37699887-37700101	MCF-7	breast:	n/a	chr14:37699980-37699996 chr14:37699981-37700002 chr14:37699982-37699995 chr14:37699982-37699995 chr14:37699979-37699997
23	CTCF	chr14:37699900-37700050	NHDF-neo	bronchial:	n/a	chr14:37699980-37699996 chr14:37699981-37700002 chr14:37699982-37699995 chr14:37699982-37699995 chr14:37699979-37699997
24	CTCF	chr14:37699920-37700070	GM12868	blood:	n/a	chr14:37699980-37699996 chr14:37699981-37700002 chr14:37699982-37699995 chr14:37699982-37699995 chr14:37699979-37699997
25	CTCF	chr14:37699885-37700092	GM13976	blood:	n/a	chr14:37699980-37699996 chr14:37699981-37700002 chr14:37699982-37699995 chr14:37699982-37699995 chr14:37699979-37699997
26	CTCF	chr14:37698419-37698486	ProgFib	skin:	n/a	n/a
27	CTCF	chr14:37700080-37700230	GM12865	blood:	n/a	n/a
28	CTCF	chr14:37699780-37700166	T-47D	breast:	n/a	chr14:37699980-37699996 chr14:37699981-37700002 chr14:37699982-37699995 chr14:37699982-37699995 chr14:37699979-37699997
29	CTCF	chr14:37700220-37700370	GM12871	blood:	n/a	n/a
30	CTCF	chr14:37699781-37700093	A549	lung:	n/a	chr14:37699980-37699996 chr14:37699981-37700002 chr14:37699982-37699995 chr14:37699982-37699995 chr14:37699979-37699997
31	CTCF	chr14:37699920-37700070	HCT-116	colon:	n/a	chr14:37699980-37699996 chr14:37699981-37700002 chr14:37699982-37699995 chr14:37699982-37699995 chr14:37699979-37699997
32	CTCF	chr14:37699900-37700050	HVMF	connective:	n/a	chr14:37699980-37699996 chr14:37699981-37700002 chr14:37699982-37699995 chr14:37699982-37699995 chr14:37699979-37699997
33	CTCF	chr14:37700133-37700134	HUVEC	blood vessel:	n/a	n/a
34	CTCF	chr14:37699851-37700140	Medullo	brain:	n/a	chr14:37699980-37699996 chr14:37699981-37700002 chr14:37699982-37699995 chr14:37699982-37699995 chr14:37699979-37699997
35	CTCF	chr14:37699900-37700050	AG04449	skin:	n/a	chr14:37699980-37699996 chr14:37699981-37700002 chr14:37699982-37699995 chr14:37699982-37699995 chr14:37699979-37699997
36	CTCF	chr14:37699920-37700070	AG09319	gingival:	n/a	chr14:37699980-37699996 chr14:37699981-37700002 chr14:37699982-37699995 chr14:37699982-37699995 chr14:37699979-37699997
37	CTCF	chr14:37699920-37700070	GM12873	blood:	n/a	chr14:37699980-37699996 chr14:37699981-37700002 chr14:37699982-37699995 chr14:37699982-37699995 chr14:37699979-37699997
38	CTCF	chr14:37699889-37700041	T-47D	breast:	n/a	chr14:37699980-37699996 chr14:37699981-37700002 chr14:37699982-37699995 chr14:37699982-37699995 chr14:37699979-37699997
39	CTCF	chr14:37699900-37700050	GM12867	blood:	n/a	chr14:37699980-37699996 chr14:37699981-37700002 chr14:37699982-37699995 chr14:37699982-37699995 chr14:37699979-37699997
40	CTCF	chr14:37699900-37700050	MCF-7	breast:	n/a	chr14:37699980-37699996 chr14:37699981-37700002 chr14:37699982-37699995 chr14:37699982-37699995 chr14:37699979-37699997
41	CTCF	chr14:37699600-37699750	HMEC	breast:	n/a	n/a
42	CTCF	chr14:37699920-37700070	GM12869	blood:	n/a	chr14:37699980-37699996 chr14:37699981-37700002 chr14:37699982-37699995 chr14:37699982-37699995 chr14:37699979-37699997
43	CTCF	chr14:37699840-37700128	HUVEC	blood vessel:	n/a	chr14:37699980-37699996 chr14:37699981-37700002 chr14:37699982-37699995 chr14:37699982-37699995 chr14:37699979-37699997
44	CTCF	chr14:37699940-37700090	HAc	cerebellar:	n/a	chr14:37699980-37699996 chr14:37699981-37700002 chr14:37699982-37699995 chr14:37699982-37699995 chr14:37699979-37699997
45	CTCF	chr14:37699920-37700070	HepG2	liver:	n/a	chr14:37699980-37699996 chr14:37699981-37700002 chr14:37699982-37699995 chr14:37699982-37699995 chr14:37699979-37699997
46	CTCF	chr14:37699860-37700010	HCM	heart:	n/a	chr14:37699980-37699996 chr14:37699981-37700002 chr14:37699982-37699995 chr14:37699982-37699995 chr14:37699979-37699997
47	CTCF	chr14:37699880-37700030	HVMF	connective:	n/a	chr14:37699980-37699996 chr14:37699981-37700002 chr14:37699982-37699995 chr14:37699982-37699995 chr14:37699979-37699997
48	CTCF	chr14:37699920-37700070	BJ	skin:	n/a	chr14:37699980-37699996 chr14:37699981-37700002 chr14:37699982-37699995 chr14:37699982-37699995 chr14:37699979-37699997
49	CTCF	chr14:37699940-37700090	HA-sp	spinal cord:	n/a	chr14:37699980-37699996 chr14:37699981-37700002 chr14:37699982-37699995 chr14:37699982-37699995 chr14:37699979-37699997
50	CTCF	chr14:37699880-37700030	HCT-116	colon:	n/a	chr14:37699980-37699996 chr14:37699981-37700002 chr14:37699982-37699995 chr14:37699982-37699995 chr14:37699979-37699997

No.	Distal block	Cell Line	Cell type
1	chr14:37697269..37708885-chr14:38056043..38068163,30	MCF-7	breast:
2	chr14:37667188..37668774-chr14:37681989..37684290,2	K562	blood:
3	chr14:37678368..37681315-chr14:38062170..38064330,2	K562	blood:
4	chr14:37679446..37681161-chr14:37683959..37685641,2	MCF-7	breast:
5	chr14:37697471..37699396-chr14:38051501..38053443,2	MCF-7	breast:
6	chr14:37696817..37699280-chr14:37707291..37710248,2	MCF-7	breast:
7	chr14:37667206..37669688-chr14:37686290..37688720,2	K562	blood:
8	chr14:37680569..37683226-chr14:37683414..37685864,2	MCF-7	breast:
9	chr14:37699430..37701952-chr14:37706278..37708031,2	MCF-7	breast:
10	chr14:37666447..37670165-chr14:37687994..37691286,5	MCF-7	breast:
11	chr14:37699926..37700451-chr14:38063417..38063967,2	MCF-7	breast:
12	chr14:37688211..37691178-chr9:38067581..38070359,2	MCF-7	breast:
13	chr14:37697987..37700834-chr14:38057234..38059879,2	MCF-7	breast:
14	chr14:37688098..37689873-chr14:37692378..37694206,2	MCF-7	breast:
15	chr14:37680569..37683226-chr14:37683414..37685864,2	MCF-7	breast:
16	chr14:37697487..37699947-chr14:38052550..38054920,2	MCF-7	breast:
17	chr14:37640266..37643741-chr14:37700089..37702308,3	MCF-7	breast:
18	chr14:37668579..37671562-chr14:37686406..37688160,2	MCF-7	breast:
19	chr14:37670963..37671524-chr14:37682927..37683529,2	MCF-7	breast:
20	chr14:37672188..37673767-chr14:37677538..37679060,2	K562	blood:
21	chr14:37641268..37642823-chr14:37697545..37700025,2	MCF-7	breast:
22	chr14:37679446..37681161-chr14:37683959..37685641,2	MCF-7	breast:
23	chr14:37698096..37705480-chr14:38061309..38066013,13	MCF-7	breast:
24	chr14:37667088..37669471-chr14:37678201..37679725,2	K562	blood:
25	chr14:37699123..37701373-chr14:37712703..37714358,2	K562	blood:
26	chr14:37619444..37620212-chr14:37699781..37700486,2	MCF-7	breast:
27	chr14:37691512..37693036-chr14:38063542..38065340,2	MCF-7	breast:
28	chr14:37619842..37620362-chr14:37699681..37700515,2	K562	blood:

Variant related genes	Relation type
MIPOL1	TF binding region
ENSG00000183032	chromatin interactions
ENSG00000139865	chromatin interactions
ENSG00000129514	chromatin interactions
ENSG00000107338	chromatin interactions
ENSG00000151338	chromatin interactions
ENSG00000258708	chromatin interactions
ENSG00000255872	chromatin interactions

Extended variants
information (count: 893 )
Associated
traits (count: 59 )

Variant overlapped rSNPs/rCNVs (count:893 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs550974850	chr14:37678251-37678252	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs144249634	chr14:37678280-37678281	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs180817023	chr14:37678315-37678316	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs185257109	chr14:37678344-37678345	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs552164910	chr14:37678404-37678405	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs535600251	chr14:37678430-37678431	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs146551538	chr14:37678444-37678445	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs534498254	chr14:37678464-37678465	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs547938561	chr14:37678479-37678480	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs567840046	chr14:37678578-37678579	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs536717009	chr14:37678616-37678617	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs140921326	chr14:37678629-37678630	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs576743266	chr14:37678679-37678680	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs60907347	chr14:37678708-37678709	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs57286495	chr14:37678709-37678710	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs60047292	chr14:37678719-37678720	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs553381870	chr14:37678724-37678725	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs150187500	chr14:37678729-37678730	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs60533834	chr14:37678738-37678739	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs58677264	chr14:37678745-37678746	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs555969267	chr14:37678747-37678748	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs575823718	chr14:37678748-37678749	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs58249685	chr14:37678770-37678771	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs58674459	chr14:37678776-37678777	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs59665906	chr14:37678779-37678780	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs149005271	chr14:37678780-37678781	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs533169046	chr14:37678806-37678807	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs147101176	chr14:37678816-37678817	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs557527256	chr14:37678821-37678822	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs559228816	chr14:37678857-37678858	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs35293661	chr14:37678954-37678955	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs528320299	chr14:37678972-37678973	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs547999670	chr14:37678987-37678988	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs567900914	chr14:37679005-37679006	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs530661485	chr14:37679016-37679017	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs550402154	chr14:37679021-37679022	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs372174353	chr14:37679059-37679060	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs74509944	chr14:37679095-37679096	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs74724082	chr14:37679097-37679098	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs546320751	chr14:37679153-37679154	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs561422680	chr14:37679186-37679187	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs57054655	chr14:37679205-37679206	Weak transcription ZNF genes & repeats Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs539071849	chr14:37679209-37679210	Weak transcription ZNF genes & repeats Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs34288919	chr14:37679264-37679265	Weak transcription ZNF genes & repeats Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs372318248	chr14:37679268-37679269	Weak transcription ZNF genes & repeats Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs9322975	chr14:37679274-37679275	Weak transcription ZNF genes & repeats Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs371453629	chr14:37679290-37679291	Weak transcription ZNF genes & repeats Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs536121242	chr14:37679291-37679292	Weak transcription ZNF genes & repeats Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs111588762	chr14:37679297-37679298	Weak transcription ZNF genes & repeats Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs556028982	chr14:37679311-37679312	Weak transcription ZNF genes & repeats Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:59)

Disease	PMID	Source
Esophageal cancer	21851588	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Retinoblastoma	21504564	CNVD
High-proliferative meningiomas	17937814	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	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
Colorectal cancer	16774939	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
Endometrioid adenocarcinoma	16974079	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Renal cell carcinoma	21668985	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Chronic myeloid leukemia	20724749	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Wilms tumour	21544195	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Burkitt''s lymphoma	19759907	CNVD
Lung cancer	18438408	CNVD
Urothelial carcinoma	21177765	CNVD
Multiple myeloma	17550852	CNVD
Breast cancer	21785460	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Lung cancer	17925434	CNVD
Colorectal cancer	16272173	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21364760	CNVD
small cell lung cancer	20016488	CNVD
abnormal development	18461090	CNVD
Prostate cancer	21298110	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	21858162	CNVD
Lung cancer	20031968	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Myelofibrosis	22110671	CNVD
Intellectual disability	22045946	CNVD
Hirschsprung''s Disease	21712996	CNVD
Cancer	21183584	CNVD
Prostate cancer	21147910	CNVD

Chromatin state (count:129 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:37667800-37680400	Weak transcription	Right Ventricle	heart
2	chr14:37668200-37682800	Weak transcription	Hela-S3	cervix
3	chr14:37668200-37686000	Weak transcription	Stomach Smooth Muscle	stomach
4	chr14:37671400-37685600	Weak transcription	Psoas Muscle	Psoas
5	chr14:37675200-37681800	Weak transcription	Aorta	Aorta
6	chr14:37675600-37681400	Weak transcription	Gastric	stomach
7	chr14:37675600-37690400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
8	chr14:37675800-37680800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
9	chr14:37675800-37681400	Weak transcription	Brain Angular Gyrus	brain
10	chr14:37675800-37693600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
11	chr14:37676000-37680600	Weak transcription	Pancreas	Pancrea
12	chr14:37676000-37681000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
13	chr14:37676000-37681800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
14	chr14:37676000-37681800	Weak transcription	Esophagus	oesophagus
15	chr14:37676000-37683000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
16	chr14:37676000-37688200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
17	chr14:37676000-37695600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
18	chr14:37676600-37681000	Weak transcription	Fetal Lung	lung
19	chr14:37676600-37688600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
20	chr14:37676600-37699400	Weak transcription	A549	lung
21	chr14:37678000-37679000	Weak transcription	Right Atrium	heart
22	chr14:37678200-37679200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
23	chr14:37679000-37679600	Enhancers	HepG2	liver
24	chr14:37679200-37680000	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
25	chr14:37679400-37679600	Enhancers	Right Atrium	heart
26	chr14:37679400-37680000	ZNF genes & repeats	Fetal Intestine Small	intestine
27	chr14:37679400-37682200	Enhancers	HUVEC	blood vessel
28	chr14:37679600-37679800	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
29	chr14:37679600-37680000	Genic enhancers	HepG2	liver
30	chr14:37679600-37680800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
31	chr14:37679800-37680000	Enhancers	Lung	lung
32	chr14:37679800-37680000	Enhancers	K562	blood
33	chr14:37680000-37680600	Weak transcription	Fetal Intestine Small	intestine
34	chr14:37680000-37682000	Strong transcription	HepG2	liver
35	chr14:37680000-37683800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
36	chr14:37680000-37693600	Weak transcription	K562	blood
37	chr14:37680200-37681000	Weak transcription	Lung	lung
38	chr14:37680200-37683200	Weak transcription	Adipose Nuclei	Adipose
39	chr14:37680600-37681000	Strong transcription	Pancreas	Pancrea
40	chr14:37680600-37682000	ZNF genes & repeats	Fetal Intestine Small	intestine
41	chr14:37680800-37681000	ZNF genes & repeats	Fetal Stomach	stomach
42	chr14:37680800-37682000	Strong transcription	Breast Myoepithelial Primary Cells	Breast
43	chr14:37680800-37685800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
44	chr14:37681000-37681400	ZNF genes & repeats	Fetal Lung	lung
45	chr14:37681000-37681400	Enhancers	Lung	lung
46	chr14:37681000-37681800	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
47	chr14:37681000-37682000	Strong transcription	Fetal Stomach	stomach
48	chr14:37681000-37694200	Weak transcription	Pancreas	Pancrea
49	chr14:37681400-37682000	Strong transcription	Gastric	stomach
50	chr14:37681400-37693400	Weak transcription	Brain Anterior Caudate	brain

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