Variant report

Variant	nsv1009708
Chromosome Location	chr4:55440944-55513275
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:256)
CpG islands
(count:306)
Chromatin interactive
region (count:28)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:256 , 50 per page) page: 1 2 3 4 5 6

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:55452430-55452826	K562	blood:	n/a	n/a
2	ARID3A	chr4:55454394-55455108	K562	blood:	n/a	n/a
3	ARID3A	chr4:55451642-55452190	K562	blood:	n/a	n/a
4	ATF1	chr4:55451820-55452249	K562	blood:	n/a	n/a
5	ATF3	chr4:55451714-55452065	K562	blood:	n/a	n/a
6	BHLHE40	chr4:55451901-55452642	K562	blood:	n/a	n/a
7	BHLHE40	chr4:55452884-55453067	K562	blood:	n/a	n/a
8	BHLHE40	chr4:55481802-55481953	K562	blood:	n/a	n/a
9	BHLHE40	chr4:55454595-55455217	K562	blood:	n/a	n/a
10	BRCA1	chr4:55442943-55443080	Hela-S3	cervix:	n/a	n/a
11	CCNT2	chr4:55451641-55452101	K562	blood:	n/a	n/a
12	CCNT2	chr4:55454457-55454926	K562	blood:	n/a	chr4:55454690-55454710
13	CEBPB	chr4:55487970-55488194	K562	blood:	n/a	n/a
14	CEBPB	chr4:55480277-55480651	IMR90	lung:	n/a	chr4:55480456-55480467
15	CEBPB	chr4:55480250-55480626	MCF-7	breast:	n/a	chr4:55480456-55480467
16	CEBPB	chr4:55480333-55480704	MCF-7	breast:	n/a	chr4:55480456-55480467
17	CEBPB	chr4:55480297-55480591	A549	lung:	n/a	chr4:55480456-55480467
18	CEBPB	chr4:55480277-55480655	K562	blood:	n/a	chr4:55480456-55480467
19	CEBPB	chr4:55487007-55487179	K562	blood:	n/a	n/a
20	CEBPB	chr4:55452578-55452765	IMR90	lung:	n/a	n/a
21	CEBPB	chr4:55442091-55442393	H1-hESC	embryonic stem cell:	n/a	n/a
22	CEBPB	chr4:55491744-55491864	H1-hESC	embryonic stem cell:	n/a	n/a
23	CEBPB	chr4:55442054-55442374	K562	blood:	n/a	n/a
24	CEBPB	chr4:55480285-55480648	HepG2	liver:	n/a	chr4:55480456-55480467
25	CEBPB	chr4:55486081-55486233	K562	blood:	n/a	n/a
26	CEBPB	chr4:55463042-55463257	IMR90	lung:	n/a	n/a
27	CEBPB	chr4:55480387-55480632	Hela-S3	cervix:	n/a	chr4:55480456-55480467
28	CEBPB	chr4:55480323-55480618	K562	blood:	n/a	chr4:55480456-55480467
29	CEBPB	chr4:55480337-55480621	ECC-1	luminal epithelium:	n/a	chr4:55480456-55480467
30	CEBPB	chr4:55480281-55480639	H1-hESC	embryonic stem cell:	n/a	chr4:55480456-55480467
31	CEBPB	chr4:55487969-55488142	H1-hESC	embryonic stem cell:	n/a	n/a
32	CEBPB	chr4:55487953-55488193	K562	blood:	n/a	n/a
33	CEBPB	chr4:55480285-55480623	ECC-1	luminal epithelium:	n/a	chr4:55480456-55480467
34	CEBPD	chr4:55454429-55454953	K562	blood:	n/a	n/a
35	CEBPD	chr4:55454456-55454975	K562	blood:	n/a	n/a
36	CHD2	chr4:55451564-55451677	K562	blood:	n/a	n/a
37	CTCF	chr4:55512820-55512970	HepG2	liver:	n/a	n/a
38	CTCF	chr4:55512720-55512870	HBMEC	blood vessel:	n/a	n/a
39	CTCF	chr4:55451707-55452048	K562	blood:	n/a	n/a
40	CTCF	chr4:55512760-55512910	GM12873	blood:	n/a	n/a
41	CTCF	chr4:55512740-55512890	NHDF-neo	bronchial:	n/a	n/a
42	CTCF	chr4:55468616-55468686	GM10248	blood:	n/a	n/a
43	CTCF	chr4:55442280-55442430	NHEK	skin:	n/a	n/a
44	CTCF	chr4:55471147-55471348	K562	blood:	n/a	n/a
45	CTCF	chr4:55471140-55471290	HAc	cerebellar:	n/a	n/a
46	CTCF	chr4:55489050-55489087	Lung_OC	lung:	n/a	n/a
47	CTCF	chr4:55499046-55499190	H1-hESC	embryonic stem cell:	n/a	n/a
48	CTCF	chr4:55471180-55471330	HepG2	liver:	n/a	n/a
49	CTCF	chr4:55471320-55471470	HRPEpiC	eye:	n/a	n/a
50	CTCF	chr4:55449076-55449112	Lung_OC	lung:	n/a	n/a

(count:306 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:55510632-55510682	HepG2	liver:	n/a
2	chr4:55510632-55510682	HepG2	liver:	n/a
3	chr4:55442371-55442421	SK-N-SH_RA	brain:	n/a
4	chr4:55499029-55499079	NHDF-neo	bronchial:	n/a
5	chr4:55499029-55499079	AG09309	skin:	n/a
6	chr4:55499029-55499079	AG04449	skin:	fetal
7	chr4:55499029-55499079	HRE	kidney:	n/a
8	chr4:55499029-55499079	BE2_C	brain:	n/a
9	chr4:55510632-55510682	HCF	heart:	n/a
10	chr4:55499384-55499434	HCF	heart:	n/a
11	chr4:55442371-55442421	BJ	skin:	n/a
12	chr4:55442371-55442421	NHDF-neo	bronchial:	n/a
13	chr4:55510632-55510682	NHBE	bronchial:	n/a
14	chr4:55510632-55510682	PANC-1	pancreas:	n/a
15	chr4:55499029-55499079	A549	lung:	n/a
16	chr4:55510632-55510682	AG09309	skin:	n/a
17	chr4:55442371-55442421	MCF10A-Er-Src	breast:	n/a
18	chr4:55510632-55510682	IMR90	lung:	fetal
19	chr4:55442371-55442421	AG09309	skin:	n/a
20	chr4:55442371-55442421	HL-60	blood:	n/a
21	chr4:55499684-55499734	PANC-1	pancreas:	n/a
22	chr4:55499384-55499434	NB4	blood:	n/a
23	chr4:55510632-55510682	AG09319	gingival:	n/a
24	chr4:55499684-55499734	Caco-2	colon:	n/a
25	chr4:55442371-55442421	NT2-D1	testis:	n/a
26	chr4:55499029-55499079	RPTEC	kidney:	n/a
27	chr4:55510632-55510682	BJ	skin:	n/a
28	chr4:55510632-55510682	NB4	blood:	n/a
29	chr4:55510632-55510682	HRCEpiC	kidney:	n/a
30	chr4:55499384-55499434	Hela-S3	cervix:	n/a
31	chr4:55499684-55499734	HMEC	breast:	n/a
32	chr4:55499384-55499434	PFSK-1	brain:	n/a
33	chr4:55499029-55499079	NH-A	brain:	n/a
34	chr4:55499029-55499079	U87	brain:	n/a
35	chr4:55499384-55499434	GM12878	blood:	n/a
36	chr4:55510632-55510682	GM06990	blood:	n/a
37	chr4:55499029-55499079	ovcar-3	ovarian:	n/a
38	chr4:55499029-55499079	HIPEpiC	eye:	n/a
39	chr4:55499384-55499434	SAEC	small airway:	n/a
40	chr4:55499384-55499434	SK-N-SH_RA	brain:	n/a
41	chr4:55510632-55510682	ProgFib	skin:	n/a
42	chr4:55510632-55510682	H1-hESC	embryonic stem cell:	embryo
43	chr4:55442371-55442421	AG10803	skin:	n/a
44	chr4:55499684-55499734	HCF	heart:	n/a
45	chr4:55499029-55499079	HCPEpiC	choroid plexus:	n/a
46	chr4:55499384-55499434	HPAEpiC	pulmonary alveolar:	n/a
47	chr4:55499684-55499734	GM12892	blood:	n/a
48	chr4:55442371-55442421	K562	blood:	n/a
49	chr4:55442371-55442421	U87	brain:	n/a
50	chr4:55499384-55499434	HepG2	liver:	n/a

(count:28 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:55445449..55448428-chr4:55450519..55452386,2	K562	blood:
2	chr4:55500450..55502781-chr4:55503910..55506040,3	K562	blood:
3	chr4:55502404..55505387-chr4:55506992..55509953,2	MCF-7	breast:
4	chr4:55440360..55442966-chr4:55443376..55446145,3	K562	blood:
5	chr4:55440360..55442966-chr4:55443376..55446145,3	K562	blood:
6	chr4:55459508..55460256-chr4:55524686..55525285,2	MCF-7	breast:
7	chr4:55437428..55440063-chr4:55440436..55443276,2	K562	blood:
8	chr4:55437669..55439693-chr4:55458499..55461313,2	K562	blood:
9	chr4:55453068..55455873-chr4:55797216..55798753,2	MCF-7	breast:
10	chr4:55451154..55453615-chr4:55461278..55463785,2	MCF-7	breast:
11	chr4:55454057..55456596-chr4:55458841..55461034,2	K562	blood:
12	chr4:55503201..55504980-chr4:55510390..55512353,2	K562	blood:
13	chr4:55503201..55504980-chr4:55510390..55512353,2	K562	blood:
14	chr4:55412214..55414847-chr4:55443164..55445591,2	K562	blood:
15	chr4:55445449..55448428-chr4:55450519..55452386,2	K562	blood:
16	chr4:55454057..55456596-chr4:55458841..55461034,2	K562	blood:
17	chr4:55502404..55505387-chr4:55506992..55509953,2	MCF-7	breast:
18	chr4:55481868..55484293-chr4:55528991..55530564,2	K562	blood:
19	chr4:55500450..55502781-chr4:55503910..55506040,3	K562	blood:
20	chr4:55451154..55453615-chr4:55461278..55463785,2	MCF-7	breast:
21	chr4:55444047..55449090-chr4:55449528..55453666,5	K562	blood:
22	chr4:55455740..55458184-chr4:55518555..55520404,2	K562	blood:
23	chr4:55452869..55453638-chr4:55708509..55709111,2	MCF-7	breast:
24	chr4:55436094..55437601-chr4:55449957..55451605,2	K562	blood:
25	chr4:55444047..55449090-chr4:55449528..55453666,5	K562	blood:
26	chr4:55440530..55442966-chr4:55443376..55445604,2	K562	blood:
27	chr4:55440530..55442966-chr4:55443376..55445604,2	K562	blood:
28	chr20:52457233..52457942-chr4:55449043..55449853,2	MCF-7	breast:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-KDR-2	chr4:55473050-55473298	XLOC_003949
2	lnc-KDR-2	chr4:55469378-55471344	ENSG00000250456
3	lnc-KDR-2	chr4:55473050-55473298	ENSG00000250456
4	lnc-KDR-2	chr4:55469380-55471344	XLOC_003949

No data

Variant related genes	Relation type
ENSG00000250456	TF binding region
ENSG00000250456	CpG island
LITAF	miRNA target sites

Extended variants
information (count: 2133 )
Associated
traits (count: 94 )

Variant overlapped rSNPs/rCNVs (count:2133 , 50 per page) page: 1 2 3 4 5 6 7 ... 43

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs563807435	chr4:55440954-55440955	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs532767914	chr4:55440955-55440956	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs542972574	chr4:55441006-55441007	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs563127307	chr4:55441019-55441020	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs529639052	chr4:55441035-55441036	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs569687798	chr4:55441147-55441148	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs73150435	chr4:55441197-55441198	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs569085382	chr4:55441219-55441220	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs566298066	chr4:55441220-55441221	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs147185188	chr4:55441243-55441244	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs140483276	chr4:55441260-55441261	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs41377746	chr4:55441280-55441281	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs537454135	chr4:55441290-55441291	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs557434461	chr4:55441307-55441308	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs567527941	chr4:55441310-55441311	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs535773071	chr4:55441319-55441320	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs555337362	chr4:55441320-55441321	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs73234229	chr4:55441338-55441339	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs534463584	chr4:55441405-55441406	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs371256097	chr4:55441450-55441451	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs147428457	chr4:55441455-55441456	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs543109755	chr4:55441502-55441503	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs376536827	chr4:55441577-55441578	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs563324739	chr4:55441599-55441600	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs532401127	chr4:55441609-55441610	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs543322401	chr4:55441610-55441611	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs550548693	chr4:55441638-55441639	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs559769626	chr4:55441660-55441661	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs76724688	chr4:55441724-55441725	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs551966230	chr4:55441757-55441758	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs77181360	chr4:55441773-55441774	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs114722982	chr4:55441784-55441785	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs550779227	chr4:55441844-55441845	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs192393970	chr4:55441852-55441853	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs149866313	chr4:55441872-55441873	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs372655720	chr4:55441896-55441897	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs565794155	chr4:55441921-55441922	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs567011356	chr4:55441925-55441926	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs377271588	chr4:55442112-55442113	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs183794218	chr4:55442127-55442128	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs536784676	chr4:55442157-55442158	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs534119786	chr4:55442159-55442160	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs556749034	chr4:55442170-55442171	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs112466671	chr4:55442171-55442172	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs542214664	chr4:55442197-55442198	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs560005578	chr4:55442285-55442286	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs11732772	chr4:55442290-55442291	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs189332876	chr4:55442293-55442294	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs565510064	chr4:55442309-55442310	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs34106577	chr4:55442310-55442311	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:94)

Disease	PMID	Source
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Glioblastoma multiforme	21080181	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Chordoma	21602918	CNVD
HIV/AIDS	22032296	CNVD
Medulloblastoma	21979893	CNVD
Neuroblastoma	18923191	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Autism	22495311	CNVD
Breast cancer	21858162	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Gastric cancer	21586687	CNVD
lymphocytic leukemia	21291569	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Non-small cell lung cancer	21829676	CNVD
Melanoma	22183965	CNVD
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Lung cancer	18438408	CNVD
Renal cell carcinoma	18194544	CNVD
Breast cancer	17603634	CNVD
Glioblastoma multiforme	21922591	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Parkinson disease	21956041	CNVD
Mental retardation	20522426	CNVD
delayed speech	20522426	CNVD
growth disorder	20522426	CNVD
Hepatocellular carcinoma	16750200	CNVD
Myxofibrosarcoma	16751306	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Acute myeloid leukemia	20729466	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Parkinson disease	18923514	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Cancer	21183584	CNVD
Breast cancer	16272173	CNVD
Glioblastoma multiforme	19435819	CNVD
Multiple myeloma	16616336	CNVD
Colorectal cancer	19359472	CNVD
Malignant mesothelioma	18160781	CNVD
Medulloblastoma	18056178	CNVD
Multiple myeloma	17077331	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
4q-syndrome	17576883	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Colorectal cancer	20709793	CNVD
Muscular dystrophy	21149563	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Cervical cancer	21062161	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	22286061	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Ovarian neoplasms	16753589	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	16608533	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Glioblastoma multiforme	21569311	CNVD
Glioblastoma	17504929	CNVD
Glioblastoma	16823502	CNVD
Melanoma	16908931	CNVD
Glioblastoma	20031968	CNVD
Medulloblastoma	19270706	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Olfactory neuroblastoma	18408657	CNVD
Basal cell lymphoma	19029149	CNVD
Diffuse large b-cell lymphoma	19029149	CNVD
Esophageal squamous carcinoma	17470683	CNVD
Rhabdomyosarcoma	16790082	CNVD
Gastrointestinal stromal cancer	17438095	CNVD
Colorectal cancer	16272173	CNVD
Lung cancer	19208797	CNVD
small cell lung cancer	20016488	CNVD
Glioblastoma multiforme	19115005	CNVD
Wilms tumour	21544195	CNVD
Glioblastoma multiforme	21138945	CNVD
Cancer	20164920	CNVD
Cancer	22183965	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Cancer	17440070	CNVD

Chromatin state (count:160 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:55438200-55441600	Enhancers	K562	blood
2	chr4:55438400-55442400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
3	chr4:55441600-55442000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
4	chr4:55441600-55450600	Weak transcription	K562	blood
5	chr4:55442000-55442200	Enhancers	iPS-15b Cell Line	embryonic stem cell
6	chr4:55442000-55442800	Enhancers	HUES64 Cell Line	embryonic stem cell
7	chr4:55442000-55442800	Enhancers	iPS-20b Cell Line	embryonic stem cell
8	chr4:55442000-55443000	Enhancers	iPS-18 Cell Line	embryonic stem cell
9	chr4:55442200-55442400	Enhancers	H9 Cell Line	embryonic stem cell
10	chr4:55442200-55442400	Enhancers	HUES48 Cell Line	embryonic stem cell
11	chr4:55442200-55442600	Enhancers	H1 Cell Line	embryonic stem cell
12	chr4:55442400-55442800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
13	chr4:55448400-55449200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
14	chr4:55449200-55452000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
15	chr4:55450600-55451400	Enhancers	K562	blood
16	chr4:55451400-55452200	Enhancers	Duodenum Mucosa	Duodenum
17	chr4:55451400-55452200	Flanking Active TSS	K562	blood
18	chr4:55451400-55453200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
19	chr4:55451400-55453800	Enhancers	Fetal Intestine Large	intestine
20	chr4:55451400-55454000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
21	chr4:55451800-55452400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
22	chr4:55451800-55452600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
23	chr4:55451800-55453200	Enhancers	NHDF-Ad	bronchial
24	chr4:55452000-55452600	Enhancers	Osteobl	bone
25	chr4:55452000-55453000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
26	chr4:55452000-55453000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
27	chr4:55452000-55453600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
28	chr4:55452000-55453800	Enhancers	Fetal Intestine Small	intestine
29	chr4:55452000-55453800	Enhancers	Sigmoid Colon	Sigmoid Colon
30	chr4:55452000-55454000	Enhancers	Rectal Mucosa Donor 31	rectum
31	chr4:55452000-55455400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
32	chr4:55452000-55455400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
33	chr4:55452000-55455800	Enhancers	HMEC	breast
34	chr4:55452000-55457200	Enhancers	NHEK	skin
35	chr4:55452000-55457600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
36	chr4:55452200-55452600	Flanking Active TSS	Duodenum Mucosa	Duodenum
37	chr4:55452200-55453000	Enhancers	Rectal Mucosa Donor 29	rectum
38	chr4:55452200-55453200	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
39	chr4:55452200-55455400	Enhancers	K562	blood
40	chr4:55452400-55452800	Enhancers	NH-A	brain
41	chr4:55452400-55453000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
42	chr4:55452400-55453000	Enhancers	Muscle Satellite Cultured Cells	--
43	chr4:55452400-55453000	Enhancers	Lung	lung
44	chr4:55452400-55453000	Enhancers	NHLF	lung
45	chr4:55452400-55453800	Enhancers	Esophagus	oesophagus
46	chr4:55452400-55453800	Enhancers	Placenta	Placenta
47	chr4:55452400-55454000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
48	chr4:55452600-55453800	Enhancers	Duodenum Mucosa	Duodenum
49	chr4:55453000-55453400	Enhancers	Stomach Mucosa	stomach
50	chr4:55453200-55454400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin

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