Variant report

Variant	nsv1013204
Chromosome Location	chr4:15762970-15836237
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1239)
CpG islands
(count:1159)
Chromatin interactive
region (count:26)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:1)

(count:1239 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

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	chr4:15773002-15773456	GM12878	blood:	n/a	n/a
3	ATF2	chr4:15779668-15780168	GM12878	blood:	n/a	n/a
4	ATF2	chr4:15780482-15781013	GM12878	blood:	n/a	n/a
5	ATF2	chr4:15767768-15768355	GM12878	blood:	n/a	n/a
6	ATF2	chr4:15810600-15811189	GM12878	blood:	n/a	n/a
7	ATF2	chr4:15796567-15797029	GM12878	blood:	n/a	n/a
8	ATF2	chr4:15783255-15783690	GM12878	blood:	n/a	n/a
9	ATF2	chr4:15786511-15787117	GM12878	blood:	n/a	n/a
10	ATF2	chr4:15786611-15786945	GM12878	blood:	n/a	n/a
11	ATF2	chr4:15810602-15811009	GM12878	blood:	n/a	n/a
12	ATF2	chr4:15783177-15783743	GM12878	blood:	n/a	n/a
13	BATF	chr4:15796641-15796857	GM12878	blood:	n/a	n/a
14	BATF	chr4:15810669-15810937	GM12878	blood:	n/a	n/a
15	BATF	chr4:15773003-15773428	GM12878	blood:	n/a	n/a
16	BATF	chr4:15783261-15783699	GM12878	blood:	n/a	n/a
17	BATF	chr4:15786622-15786889	GM12878	blood:	n/a	n/a
18	BATF	chr4:15773053-15773367	GM12878	blood:	n/a	n/a
19	BATF	chr4:15780602-15780822	GM12878	blood:	n/a	n/a
20	BATF	chr4:15810574-15811109	GM12878	blood:	n/a	n/a
21	BATF	chr4:15783150-15783781	GM12878	blood:	n/a	n/a
22	BATF	chr4:15786518-15786925	GM12878	blood:	n/a	n/a
23	BCL11A	chr4:15783198-15783725	GM12878	blood:	n/a	n/a
24	BCL11A	chr4:15786525-15786942	GM12878	blood:	n/a	chr4:15786784-15786793 chr4:15786727-15786736
25	BCL11A	chr4:15810592-15811057	GM12878	blood:	n/a	n/a
26	BCL11A	chr4:15834755-15834971	GM12878	blood:	n/a	n/a
27	BCL11A	chr4:15810571-15811023	GM12878	blood:	n/a	n/a
28	BCL11A	chr4:15786619-15786864	GM12878	blood:	n/a	chr4:15786784-15786793 chr4:15786727-15786736
29	BCL11A	chr4:15780532-15780916	GM12878	blood:	n/a	n/a
30	BCL11A	chr4:15780529-15780822	GM12878	blood:	n/a	n/a
31	BCL3	chr4:15796609-15796941	GM12878	blood:	n/a	n/a
32	BCL3	chr4:15786543-15786895	GM12878	blood:	n/a	chr4:15786784-15786793 chr4:15786727-15786736
33	BCLAF1	chr4:15779745-15780156	GM12878	blood:	n/a	n/a
34	BCLAF1	chr4:15786466-15787092	GM12878	blood:	n/a	chr4:15786784-15786793 chr4:15786727-15786736
35	BCLAF1	chr4:15780410-15781105	GM12878	blood:	n/a	chr4:15780473-15780486
36	BCLAF1	chr4:15783161-15783754	GM12878	blood:	n/a	n/a
37	BCLAF1	chr4:15779712-15780256	GM12878	blood:	n/a	n/a
38	BCLAF1	chr4:15780383-15780981	GM12878	blood:	n/a	chr4:15780473-15780486
39	BHLHE40	chr4:15807497-15807543	K562	blood:	n/a	n/a
40	BHLHE40	chr4:15834966-15834971	GM12878	blood:	n/a	n/a
41	BHLHE40	chr4:15779676-15781114	GM12878	blood:	n/a	chr4:15780312-15780328
42	BHLHE40	chr4:15773057-15773402	GM12878	blood:	n/a	n/a
43	BHLHE40	chr4:15810619-15811261	GM12878	blood:	n/a	n/a
44	BHLHE40	chr4:15783253-15783720	GM12878	blood:	n/a	n/a
45	BHLHE40	chr4:15796707-15796891	GM12878	blood:	n/a	n/a
46	BHLHE40	chr4:15767864-15768326	GM12878	blood:	n/a	n/a
47	BHLHE40	chr4:15786540-15786922	GM12878	blood:	n/a	n/a
48	CCNT2	chr4:15780287-15780560	K562	blood:	n/a	n/a
49	CEBPB	chr4:15781009-15781855	A549	lung:	n/a	chr4:15781248-15781259
50	CEBPB	chr4:15780494-15781031	GM12878	blood:	n/a	n/a

(count:1159 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:15780011-15780061	NHDF-neo	bronchial:	n/a
2	chr4:15780728-15780778	PFSK-1	brain:	n/a
3	chr4:15780849-15780899	SK-N-SH_RA	brain:	n/a
4	chr4:15784659-15784709	CMK	blood:	n/a
5	chr4:15776675-15776725	HCPEpiC	choroid plexus:	n/a
6	chr4:15779392-15779442	H1-hESC	embryonic stem cell:	embryo
7	chr4:15779642-15779692	HRPEpiC	eye:	n/a
8	chr4:15788633-15788683	K562	blood:	n/a
9	chr4:15788740-15788790	SAEC	small airway:	n/a
10	chr4:15780238-15780288	PFSK-1	brain:	n/a
11	chr4:15780728-15780778	GM12892	blood:	n/a
12	chr4:15780728-15780778	PANC-1	pancreas:	n/a
13	chr4:15776675-15776725	ProgFib	skin:	n/a
14	chr4:15779999-15780049	ProgFib	skin:	n/a
15	chr4:15779392-15779442	BE2_C	brain:	n/a
16	chr4:15780728-15780778	MCF-7	breast:	n/a
17	chr4:15780011-15780061	Hela-S3	cervix:	n/a
18	chr4:15779999-15780049	HRE	kidney:	n/a
19	chr4:15779999-15780049	HRPEpiC	eye:	n/a
20	chr4:15779392-15779442	NB4	blood:	n/a
21	chr4:15780728-15780778	ProgFib	skin:	n/a
22	chr4:15776675-15776725	A549	lung:	n/a
23	chr4:15789397-15789447	MCF-7	breast:	n/a
24	chr4:15779642-15779692	HUVEC	blood vessel:	n/a
25	chr4:15780306-15780356	Hela-S3	cervix:	n/a
26	chr4:15780849-15780899	HCPEpiC	choroid plexus:	n/a
27	chr4:15779879-15779929	GM12892	blood:	n/a
28	chr4:15780849-15780899	HL-60	blood:	n/a
29	chr4:15780306-15780356	BJ	skin:	n/a
30	chr4:15780238-15780288	MCF-7	breast:	n/a
31	chr4:15779709-15779759	Jurkat	blood:	n/a
32	chr4:15788740-15788790	AG09319	gingival:	n/a
33	chr4:15780306-15780356	NHDF-neo	bronchial:	n/a
34	chr4:15780728-15780778	SK-N-SH	brain:	n/a
35	chr4:15779879-15779929	AG09319	gingival:	n/a
36	chr4:15779999-15780049	SK-N-MC	brain:	n/a
37	chr4:15776675-15776725	SK-N-MC	brain:	n/a
38	chr4:15789251-15789301	AG09319	gingival:	n/a
39	chr4:15784659-15784709	NHDF-neo	bronchial:	n/a
40	chr4:15779642-15779692	HCPEpiC	choroid plexus:	n/a
41	chr4:15788633-15788683	BE2_C	brain:	n/a
42	chr4:15779999-15780049	NHBE	bronchial:	n/a
43	chr4:15784659-15784709	SKMC	muscle:	n/a
44	chr4:15779392-15779442	LNCaP	prostate:	n/a
45	chr4:15789251-15789301	AoSMC	blood vessel:	n/a
46	chr4:15784659-15784709	HUVEC	blood vessel:	n/a
47	chr4:15781202-15781252	HRPEpiC	eye:	n/a
48	chr4:15776675-15776725	HNPCEpiC	eye:	n/a
49	chr4:15788740-15788790	HCT-116	colon:	n/a
50	chr4:15780849-15780899	NT2-D1	testis:	n/a

(count:26 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:15480370..15481153-chr4:15806963..15807469,2	K562	blood:
2	chr4:15481667..15484454-chr4:15772642..15775403,2	MCF-7	breast:
3	chr4:15806938..15808731-chr4:15956942..15959100,23	MCF-7	breast:
4	chr4:15807510..15808449-chr4:16002625..16003288,4	MCF-7	breast:
5	chr4:15807387..15808181-chr4:15965507..15966376,2	MCF-7	breast:
6	chr4:15807425..15808029-chr4:15884349..15884905,2	MCF-7	breast:
7	chr4:15806892..15808411-chr4:15957025..15958377,7	MCF-7	breast:
8	chr4:15826370..15828037-chr4:15841878..15844425,2	K562	blood:
9	chr4:15807414..15807927-chr4:16266396..16267022,2	K562	blood:
10	chr4:15807303..15808035-chr4:16206943..16207548,2	MCF-7	breast:
11	chr4:15480670..15481284-chr4:15807016..15807786,2	MCF-7	breast:
12	chr4:15807385..15808050-chr4:15955550..15956370,2	MCF-7	breast:
13	chr4:15771423..15774001-chr4:15776022..15777670,2	K562	blood:
14	chr4:15826917..15827917-chr8:136455043..136455804,2	MCF-7	breast:
15	chr4:15807924..15808450-chr4:15957421..15958125,3	K562	blood:
16	chr4:15807264..15808022-chr4:16200416..16201272,3	MCF-7	breast:
17	chr4:15834749..15838947-chr4:15851334..15854904,3	K562	blood:
18	chr4:15832292..15833949-chr4:15839001..15841851,2	MCF-7	breast:
19	chr4:15807943..15808473-chr4:15883958..15884923,2	K562	blood:
20	chr4:15771423..15774001-chr4:15776022..15777670,2	K562	blood:
21	chr4:15806718..15807918-chr4:15957577..15958542,9	K562	blood:
22	chr4:15745915..15748047-chr4:15772262..15775120,2	MCF-7	breast:
23	chr4:15809317..15811696-chr4:15960415..15963386,3	MCF-7	breast:
24	chr4:15655671..15657885-chr4:15800456..15802439,2	MCF-7	breast:
25	chr4:15480282..15481134-chr4:15806986..15807971,3	MCF-7	breast:
26	chr4:15731707..15732212-chr4:15806910..15807470,2	K562	blood:

(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: 2798 )
Associated
traits (count: 50 )

Variant overlapped rSNPs/rCNVs (count:2798 , 50 per page) page: 1 2 3 4 5 6 7 ... 56

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs16892391	chr4:15762970-15762971	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs548062620	chr4:15763083-15763084	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs561419774	chr4:15763101-15763102	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs140803198	chr4:15763135-15763136	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs7681005	chr4:15763167-15763168	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs570992568	chr4:15763221-15763222	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs567621705	chr4:15763271-15763272	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs538386085	chr4:15763394-15763395	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs189035365	chr4:15763438-15763439	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs150142156	chr4:15763471-15763472	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs192653278	chr4:15763475-15763476	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs565294680	chr4:15763532-15763533	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs138716865	chr4:15763545-15763546	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs554891687	chr4:15763551-15763552	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs556748731	chr4:15763570-15763571	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs574631363	chr4:15763573-15763574	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs537283091	chr4:15763598-15763599	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs184271994	chr4:15763602-15763603	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs113721048	chr4:15763647-15763648	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs556849656	chr4:15763689-15763690	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs376475177	chr4:15763705-15763706	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs76162627	chr4:15763809-15763810	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs10601665	chr4:15763840-15763841	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs376097841	chr4:15763841-15763842	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs142777025	chr4:15763908-15763909	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs545478705	chr4:15763921-15763922	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs201305423	chr4:15763936-15763937	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs10601666	chr4:15763939-15763940	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs200051433	chr4:15763940-15763941	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs11470387	chr4:15763948-15763949	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs565283668	chr4:15763959-15763960	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs552813605	chr4:15763962-15763963	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs539334366	chr4:15763965-15763966	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs572518602	chr4:15763981-15763982	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs559023824	chr4:15764045-15764046	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs7340802	chr4:15764049-15764050	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs187475148	chr4:15764086-15764087	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs561659527	chr4:15764120-15764121	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs115357644	chr4:15764147-15764148	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs550368032	chr4:15764157-15764158	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs563694288	chr4:15764167-15764168	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs147346386	chr4:15764240-15764241	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs191562549	chr4:15764253-15764254	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs565430159	chr4:15764260-15764261	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs558498131	chr4:15764294-15764295	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs547857508	chr4:15764340-15764341	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs137941047	chr4:15764377-15764378	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs536913492	chr4:15764385-15764386	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs74469889	chr4:15764410-15764411	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs577067188	chr4:15764453-15764454	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:50)

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
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:1157 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:15752600-15767600	Weak transcription	Fetal Intestine Small	intestine
2	chr4:15759200-15765400	Weak transcription	Thymus	Thymus
3	chr4:15759200-15765600	Enhancers	Dnd41	blood
4	chr4:15759200-15766400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
5	chr4:15759200-15767800	Weak transcription	Primary monocytes fromperipheralblood	blood
6	chr4:15759400-15763400	Weak transcription	Primary hematopoietic stem cells	blood
7	chr4:15759600-15763000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
8	chr4:15759600-15763400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
9	chr4:15759800-15766200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
10	chr4:15760000-15767200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
11	chr4:15760000-15767400	Weak transcription	Primary T helper cells PMA-I stimulated	--
12	chr4:15760200-15767200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
13	chr4:15761000-15767200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
14	chr4:15761200-15763000	Weak transcription	Primary T cells from cord blood	blood
15	chr4:15762000-15764200	Weak transcription	Primary neutrophils fromperipheralblood	blood
16	chr4:15762000-15767800	Weak transcription	Monocytes-CD14+_RO01746	blood
17	chr4:15762800-15763800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
18	chr4:15762800-15766200	Weak transcription	Fetal Thymus	thymus
19	chr4:15763000-15763400	Enhancers	Primary T cells from cord blood	blood
20	chr4:15763000-15769800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
21	chr4:15763400-15763600	Enhancers	GM12878-XiMat	blood
22	chr4:15763400-15763800	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
23	chr4:15763400-15764000	Enhancers	Primary hematopoietic stem cells	blood
24	chr4:15763400-15766400	Weak transcription	Primary T cells from cord blood	blood
25	chr4:15763600-15767000	Weak transcription	GM12878-XiMat	blood
26	chr4:15763800-15764200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
27	chr4:15763800-15766200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
28	chr4:15764000-15766200	Weak transcription	Primary hematopoietic stem cells	blood
29	chr4:15764200-15764400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
30	chr4:15764200-15764800	Strong transcription	Primary neutrophils fromperipheralblood	blood
31	chr4:15764400-15764600	Enhancers	Primary T regulatory cells fromperipheralblood	blood
32	chr4:15764400-15765400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
33	chr4:15764600-15767400	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
34	chr4:15764800-15775800	Weak transcription	Primary neutrophils fromperipheralblood	blood
35	chr4:15765400-15767000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
36	chr4:15765400-15767200	Enhancers	Thymus	Thymus
37	chr4:15765600-15765800	Enhancers	Fetal Lung	lung
38	chr4:15765600-15768000	Flanking Active TSS	Dnd41	blood
39	chr4:15766200-15766400	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
40	chr4:15766200-15767800	Enhancers	Fetal Thymus	thymus
41	chr4:15766200-15769000	Enhancers	Primary hematopoietic stem cells	blood
42	chr4:15766200-15769800	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
43	chr4:15766400-15767200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
44	chr4:15766400-15767200	Enhancers	Spleen	Spleen
45	chr4:15766400-15768200	Enhancers	Primary T cells from cord blood	blood
46	chr4:15766400-15769000	Enhancers	Primary hematopoietic stem cells short term culture	blood
47	chr4:15766600-15767200	Enhancers	Left Ventricle	heart
48	chr4:15766800-15768800	Enhancers	Primary B cells from peripheral blood	blood
49	chr4:15766800-15770000	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
50	chr4:15766800-15771000	Enhancers	Primary T helper cells fromperipheralblood	blood

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