Variant report

Variant	nsv1010597
Chromosome Location	chr4:15776181-15836237
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1145)
CpG islands
(count:1162)
Chromatin interactive
region (count:23)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:1)

(count:1145 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:15781018-15781370	HepG2	liver:	n/a	n/a
2	ATF2	chr4:15779668-15780168	GM12878	blood:	n/a	n/a
3	ATF2	chr4:15786511-15787117	GM12878	blood:	n/a	n/a
4	ATF2	chr4:15810602-15811009	GM12878	blood:	n/a	n/a
5	ATF2	chr4:15783255-15783690	GM12878	blood:	n/a	n/a
6	ATF2	chr4:15810600-15811189	GM12878	blood:	n/a	n/a
7	ATF2	chr4:15780482-15781013	GM12878	blood:	n/a	n/a
8	ATF2	chr4:15786611-15786945	GM12878	blood:	n/a	n/a
9	ATF2	chr4:15783177-15783743	GM12878	blood:	n/a	n/a
10	ATF2	chr4:15796567-15797029	GM12878	blood:	n/a	n/a
11	BATF	chr4:15786518-15786925	GM12878	blood:	n/a	n/a
12	BATF	chr4:15810574-15811109	GM12878	blood:	n/a	n/a
13	BATF	chr4:15783150-15783781	GM12878	blood:	n/a	n/a
14	BATF	chr4:15783261-15783699	GM12878	blood:	n/a	n/a
15	BATF	chr4:15796641-15796857	GM12878	blood:	n/a	n/a
16	BATF	chr4:15780602-15780822	GM12878	blood:	n/a	n/a
17	BATF	chr4:15786622-15786889	GM12878	blood:	n/a	n/a
18	BATF	chr4:15810669-15810937	GM12878	blood:	n/a	n/a
19	BCL11A	chr4:15786619-15786864	GM12878	blood:	n/a	chr4:15786784-15786793 chr4:15786727-15786736
20	BCL11A	chr4:15834755-15834971	GM12878	blood:	n/a	n/a
21	BCL11A	chr4:15783198-15783725	GM12878	blood:	n/a	n/a
22	BCL11A	chr4:15810592-15811057	GM12878	blood:	n/a	n/a
23	BCL11A	chr4:15810571-15811023	GM12878	blood:	n/a	n/a
24	BCL11A	chr4:15780532-15780916	GM12878	blood:	n/a	n/a
25	BCL11A	chr4:15780529-15780822	GM12878	blood:	n/a	n/a
26	BCL11A	chr4:15786525-15786942	GM12878	blood:	n/a	chr4:15786784-15786793 chr4:15786727-15786736
27	BCL3	chr4:15786543-15786895	GM12878	blood:	n/a	chr4:15786784-15786793 chr4:15786727-15786736
28	BCL3	chr4:15796609-15796941	GM12878	blood:	n/a	n/a
29	BCLAF1	chr4:15783161-15783754	GM12878	blood:	n/a	n/a
30	BCLAF1	chr4:15779712-15780256	GM12878	blood:	n/a	n/a
31	BCLAF1	chr4:15779745-15780156	GM12878	blood:	n/a	n/a
32	BCLAF1	chr4:15780410-15781105	GM12878	blood:	n/a	chr4:15780473-15780486
33	BCLAF1	chr4:15786466-15787092	GM12878	blood:	n/a	chr4:15786784-15786793 chr4:15786727-15786736
34	BCLAF1	chr4:15780383-15780981	GM12878	blood:	n/a	chr4:15780473-15780486
35	BHLHE40	chr4:15786540-15786922	GM12878	blood:	n/a	n/a
36	BHLHE40	chr4:15796707-15796891	GM12878	blood:	n/a	n/a
37	BHLHE40	chr4:15779676-15781114	GM12878	blood:	n/a	chr4:15780312-15780328
38	BHLHE40	chr4:15783253-15783720	GM12878	blood:	n/a	n/a
39	BHLHE40	chr4:15810619-15811261	GM12878	blood:	n/a	n/a
40	BHLHE40	chr4:15834966-15834971	GM12878	blood:	n/a	n/a
41	BHLHE40	chr4:15807497-15807543	K562	blood:	n/a	n/a
42	CCNT2	chr4:15780287-15780560	K562	blood:	n/a	n/a
43	CEBPB	chr4:15799418-15799610	HepG2	liver:	n/a	n/a
44	CEBPB	chr4:15832206-15832400	H1-hESC	embryonic stem cell:	n/a	chr4:15832266-15832277
45	CEBPB	chr4:15832126-15832423	A549	lung:	n/a	chr4:15832266-15832277
46	CEBPB	chr4:15813738-15813925	HepG2	liver:	n/a	n/a
47	CEBPB	chr4:15799473-15799647	A549	lung:	n/a	n/a
48	CEBPB	chr4:15781009-15781855	A549	lung:	n/a	chr4:15781248-15781259
49	CEBPB	chr4:15780969-15781416	A549	lung:	n/a	chr4:15781248-15781259
50	CEBPB	chr4:15781028-15781805	HepG2	liver:	n/a	chr4:15781248-15781259

(count:1162 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:15780306-15780356	SK-N-SH	brain:	n/a
2	chr4:15779709-15779759	HRCEpiC	kidney:	n/a
3	chr4:15788633-15788683	GM12878	blood:	n/a
4	chr4:15780306-15780356	SK-N-SH	brain:	n/a
5	chr4:15779709-15779759	HRCEpiC	kidney:	n/a
6	chr4:15788633-15788683	GM12878	blood:	n/a
7	chr4:15779642-15779692	T-47D	breast:	n/a
8	chr4:15779999-15780049	AG09309	skin:	n/a
9	chr4:15788633-15788683	Caco-2	colon:	n/a
10	chr4:15776675-15776725	Caco-2	colon:	n/a
11	chr4:15779642-15779692	AG09309	skin:	n/a
12	chr4:15779709-15779759	HEK293	kidney:	embryo
13	chr4:15780728-15780778	HRPEpiC	eye:	n/a
14	chr4:15780011-15780061	HRPEpiC	eye:	n/a
15	chr4:15780306-15780356	GM06990	blood:	n/a
16	chr4:15779879-15779929	HEK293	kidney:	embryo
17	chr4:15779392-15779442	HCM	heart:	n/a
18	chr4:15780011-15780061	NT2-D1	testis:	n/a
19	chr4:15780238-15780288	GM12892	blood:	n/a
20	chr4:15779879-15779929	AG09319	gingival:	n/a
21	chr4:15780011-15780061	ProgFib	skin:	n/a
22	chr4:15788740-15788790	ovcar-3	ovarian:	n/a
23	chr4:15788633-15788683	AG10803	skin:	n/a
24	chr4:15780238-15780288	BE2_C	brain:	n/a
25	chr4:15779999-15780049	AG10803	skin:	n/a
26	chr4:15780522-15780572	GM06990	blood:	n/a
27	chr4:15779709-15779759	HCPEpiC	choroid plexus:	n/a
28	chr4:15781202-15781252	A549	lung:	n/a
29	chr4:15784659-15784709	HRPEpiC	eye:	n/a
30	chr4:15779642-15779692	IMR90	lung:	fetal
31	chr4:15788740-15788790	PFSK-1	brain:	n/a
32	chr4:15781095-15781145	IMR90	lung:	fetal
33	chr4:15779392-15779442	Hepatocyte	liver:	n/a
34	chr4:15779392-15779442	T-47D	breast:	n/a
35	chr4:15780849-15780899	NHBE	bronchial:	n/a
36	chr4:15784659-15784709	PANC-1	pancreas:	n/a
37	chr4:15779999-15780049	SKMC	muscle:	n/a
38	chr4:15780849-15780899	SK-N-MC	brain:	n/a
39	chr4:15781095-15781145	PANC-1	pancreas:	n/a
40	chr4:15789251-15789301	Hela-S3	cervix:	n/a
41	chr4:15779709-15779759	BE2_C	brain:	n/a
42	chr4:15779999-15780049	CMK	blood:	n/a
43	chr4:15779392-15779442	HEEpiC	esophagus:	n/a
44	chr4:15780306-15780356	PFSK-1	brain:	n/a
45	chr4:15780728-15780778	GM06990	blood:	n/a
46	chr4:15780728-15780778	AoSMC	blood vessel:	n/a
47	chr4:15780306-15780356	H1-hESC	embryonic stem cell:	embryo
48	chr4:15780238-15780288	HCPEpiC	choroid plexus:	n/a
49	chr4:15780728-15780778	ECC-1	luminal epithelium:	n/a
50	chr4:15789251-15789301	AG04449	skin:	fetal

(count:23 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:15731707..15732212-chr4:15806910..15807470,2	K562	blood:
2	chr4:15809317..15811696-chr4:15960415..15963386,3	MCF-7	breast:
3	chr4:15807303..15808035-chr4:16206943..16207548,2	MCF-7	breast:
4	chr4:15807924..15808450-chr4:15957421..15958125,3	K562	blood:
5	chr4:15806718..15807918-chr4:15957577..15958542,9	K562	blood:
6	chr4:15771423..15774001-chr4:15776022..15777670,2	K562	blood:
7	chr4:15480282..15481134-chr4:15806986..15807971,3	MCF-7	breast:
8	chr4:15807414..15807927-chr4:16266396..16267022,2	K562	blood:
9	chr4:15806938..15808731-chr4:15956942..15959100,23	MCF-7	breast:
10	chr4:15807425..15808029-chr4:15884349..15884905,2	MCF-7	breast:
11	chr4:15807943..15808473-chr4:15883958..15884923,2	K562	blood:
12	chr4:15480670..15481284-chr4:15807016..15807786,2	MCF-7	breast:
13	chr4:15807264..15808022-chr4:16200416..16201272,3	MCF-7	breast:
14	chr4:15480370..15481153-chr4:15806963..15807469,2	K562	blood:
15	chr4:15807510..15808449-chr4:16002625..16003288,4	MCF-7	breast:
16	chr4:15834749..15838947-chr4:15851334..15854904,3	K562	blood:
17	chr4:15832292..15833949-chr4:15839001..15841851,2	MCF-7	breast:
18	chr4:15826917..15827917-chr8:136455043..136455804,2	MCF-7	breast:
19	chr4:15655671..15657885-chr4:15800456..15802439,2	MCF-7	breast:
20	chr4:15826370..15828037-chr4:15841878..15844425,2	K562	blood:
21	chr4:15807385..15808050-chr4:15955550..15956370,2	MCF-7	breast:
22	chr4:15806892..15808411-chr4:15957025..15958377,7	MCF-7	breast:
23	chr4:15807387..15808181-chr4:15965507..15966376,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FBXL5-9	chr4:15779187-15780675	NONHSAT095646

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	CD38	hsa-miR-335-5p	chr4:15827318-15827342

Variant related genes	Relation type
CD38	TF binding region
CD38	CpG island
ENSG00000118564	chromatin interactions
ENSG00000048342	chromatin interactions

Extended variants
information (count: 2273 )
Associated
traits (count: 49 )

Variant overlapped rSNPs/rCNVs (count:2273 , 50 per page) page: 1 2 3 4 5 6 7 ... 46

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6831585	chr4:15776181-15776182	Strong transcription Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs145146576	chr4:15776195-15776196	Strong transcription Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs9637595	chr4:15776199-15776200	Strong transcription Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs576401028	chr4:15776295-15776296	Bivalent Enhancer Strong transcription Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs539010071	chr4:15776373-15776374	Bivalent Enhancer Strong transcription Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs142099513	chr4:15776434-15776435	Strong transcription Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs572668517	chr4:15776456-15776457	Strong transcription Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs566507218	chr4:15776459-15776460	Strong transcription Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs575050600	chr4:15776478-15776479	Strong transcription Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs115726192	chr4:15776514-15776515	Strong transcription Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs561102645	chr4:15776523-15776524	Strong transcription Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs574196641	chr4:15776529-15776530	Strong transcription Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs543158295	chr4:15776567-15776568	Strong transcription Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs563033234	chr4:15776581-15776582	Strong transcription Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs532044552	chr4:15776586-15776587	Strong transcription Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs552129127	chr4:15776601-15776602	Strong transcription Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs559403095	chr4:15776631-15776632	Strong transcription Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs542077545	chr4:15776653-15776654	Strong transcription Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs548409546	chr4:15776656-15776657	Strong transcription Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs568310467	chr4:15776683-15776684	Strong transcription Enhancers Weak transcription Flanking Active TSS	CpG island	1 gene(s)	Overlapped CNVs	n/a
21	rs537236031	chr4:15776776-15776777	Strong transcription Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs550334283	chr4:15776835-15776836	Strong transcription Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs66998564	chr4:15776861-15776862	Strong transcription Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
24	rs538682620	chr4:15776867-15776868	Strong transcription Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs558874100	chr4:15776974-15776975	Strong transcription Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs572657516	chr4:15777047-15777048	Strong transcription Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs185186959	chr4:15777060-15777061	Strong transcription Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs372174655	chr4:15777062-15777063	Strong transcription Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs574731376	chr4:15777067-15777068	Strong transcription Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs190074039	chr4:15777098-15777099	Strong transcription Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs146375561	chr4:15777165-15777166	Strong transcription Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs576838202	chr4:15777265-15777266	Strong transcription Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs114823994	chr4:15777292-15777293	Strong transcription Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs552164221	chr4:15777328-15777329	Strong transcription Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs181148901	chr4:15777387-15777388	Strong transcription Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs139304802	chr4:15777413-15777414	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs548544910	chr4:15777502-15777503	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs561950150	chr4:15777546-15777547	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs185500917	chr4:15777553-15777554	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs13105588	chr4:15777582-15777583	Weak transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
41	rs570064826	chr4:15777589-15777590	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs28429904	chr4:15777596-15777597	Weak transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs552289757	chr4:15777602-15777603	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs371751229	chr4:15777607-15777608	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs144224511	chr4:15777655-15777656	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs187961807	chr4:15777674-15777675	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs201508372	chr4:15777784-15777785	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs554876821	chr4:15777860-15777861	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs6449180	chr4:15777881-15777882	Weak transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs148707834	chr4:15777893-15777894	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:49)

Disease	PMID	Source
Oral squamous cell carcinoma	17134496	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17603634	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Colorectal cancer	19359472	CNVD
Neuroblastoma	17533364	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Cancer	21637783	CNVD
Melanoma	21693616	CNVD
Squamous cell cancer	21044232	CNVD
Colorectal cancer	20709793	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Non-small cell lung cancer	21044232	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	17387387	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Cervical cancer	21062161	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Glioblastoma multiforme	21080181	CNVD
Chordoma	21602918	CNVD
HIV/AIDS	22032296	CNVD
Neuroblastoma	18923191	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Breast cancer	21785460	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Breast cancer	21509527	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21858162	CNVD
small cell lung cancer	20016488	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Cancer	21183584	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Gastric cancer	21586687	CNVD
Breast cancer	17133270	CNVD
lymphocytic leukemia	21291569	CNVD
Breast cancer	16608533	CNVD
Non-small cell lung cancer	21829676	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:985 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:15767200-15779400	Weak transcription	Spleen	Spleen
2	chr4:15768200-15777200	Enhancers	Fetal Thymus	thymus
3	chr4:15769200-15778600	Weak transcription	Skeletal Muscle Female	skeletal muscle
4	chr4:15771200-15779400	Weak transcription	Primary T cells fromperipheralblood	blood
5	chr4:15772400-15776200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
6	chr4:15772400-15776600	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
7	chr4:15772800-15776200	Enhancers	Duodenum Mucosa	Duodenum
8	chr4:15772800-15778000	Flanking Active TSS	Dnd41	blood
9	chr4:15773600-15779200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
10	chr4:15774000-15779800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
11	chr4:15774400-15779400	Weak transcription	Primary hematopoietic stem cells	blood
12	chr4:15774400-15779600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
13	chr4:15774400-15780000	Weak transcription	Sigmoid Colon	Sigmoid Colon
14	chr4:15774400-15780000	Weak transcription	Small Intestine	intestine
15	chr4:15774600-15779200	Weak transcription	Primary T helper cells fromperipheralblood	blood
16	chr4:15774600-15779600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
17	chr4:15774800-15776400	Enhancers	Stomach Mucosa	stomach
18	chr4:15774800-15779000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
19	chr4:15775200-15779200	Weak transcription	Primary T helper cells PMA-I stimulated	--
20	chr4:15775400-15776200	Enhancers	GM12878-XiMat	blood
21	chr4:15775400-15776400	Enhancers	Hela-S3	cervix
22	chr4:15775400-15776600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
23	chr4:15775400-15776800	Enhancers	Primary T cells from cord blood	blood
24	chr4:15775600-15776200	Enhancers	Rectal Mucosa Donor 31	rectum
25	chr4:15775800-15776200	Bivalent Enhancer	HepG2	liver
26	chr4:15775800-15777400	Strong transcription	Primary neutrophils fromperipheralblood	blood
27	chr4:15775800-15779000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
28	chr4:15776000-15776200	Flanking Active TSS	A549	lung
29	chr4:15776000-15777400	Strong transcription	Monocytes-CD14+_RO01746	blood
30	chr4:15776000-15778600	Weak transcription	Thymus	Thymus
31	chr4:15776000-15779600	Weak transcription	Rectal Mucosa Donor 29	rectum
32	chr4:15776200-15776400	Bivalent Enhancer	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
33	chr4:15776200-15777400	Enhancers	A549	lung
34	chr4:15776200-15778600	Weak transcription	GM12878-XiMat	blood
35	chr4:15776200-15779000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
36	chr4:15776200-15779200	Weak transcription	Duodenum Mucosa	Duodenum
37	chr4:15776200-15779400	Weak transcription	Rectal Mucosa Donor 31	rectum
38	chr4:15776200-15780000	Weak transcription	Right Atrium	heart
39	chr4:15776600-15779600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
40	chr4:15776800-15777000	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin03	Skin
41	chr4:15776800-15779200	Weak transcription	Primary T cells from cord blood	blood
42	chr4:15777200-15778600	Weak transcription	Fetal Thymus	thymus
43	chr4:15777400-15779600	Weak transcription	A549	lung
44	chr4:15777400-15779600	Weak transcription	Monocytes-CD14+_RO01746	blood
45	chr4:15777400-15779800	Weak transcription	Primary neutrophils fromperipheralblood	blood
46	chr4:15778000-15778400	Enhancers	Dnd41	blood
47	chr4:15778400-15779800	Flanking Active TSS	Dnd41	blood
48	chr4:15778600-15778800	Enhancers	Thymus	Thymus
49	chr4:15778600-15779000	Enhancers	Skeletal Muscle Female	skeletal muscle
50	chr4:15778600-15779200	Enhancers	GM12878-XiMat	blood

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