Variant report

Variant	nsv508274
Chromosome Location	chr4:10179291-10239403
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:716)
CpG islands
(count:0)
Chromatin interactive
region (count:90)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:716 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:10188308-10188961	K562	blood:	n/a	n/a
2	ARID3A	chr4:10185222-10185607	K562	blood:	n/a	chr4:10185454-10185470
3	ARID3A	chr4:10206944-10207053	HepG2	liver:	n/a	n/a
4	ARID3A	chr4:10206912-10207070	K562	blood:	n/a	n/a
5	ARID3A	chr4:10182036-10184108	K562	blood:	n/a	n/a
6	ARID3A	chr4:10186847-10188023	K562	blood:	n/a	n/a
7	ARID3A	chr4:10202441-10202778	K562	blood:	n/a	n/a
8	ATF1	chr4:10188186-10188661	K562	blood:	n/a	n/a
9	ATF1	chr4:10187244-10187892	K562	blood:	n/a	n/a
10	ATF1	chr4:10184693-10185042	K562	blood:	n/a	n/a
11	ATF1	chr4:10199601-10200004	K562	blood:	n/a	n/a
12	ATF1	chr4:10182216-10183403	K562	blood:	n/a	n/a
13	ATF3	chr4:10182376-10183375	K562	blood:	n/a	n/a
14	ATF3	chr4:10187352-10187768	K562	blood:	n/a	n/a
15	BACH1	chr4:10203548-10203807	K562	blood:	n/a	n/a
16	BACH1	chr4:10236419-10236458	K562	blood:	n/a	n/a
17	BACH1	chr4:10182278-10183266	K562	blood:	n/a	n/a
18	BACH1	chr4:10187292-10187596	K562	blood:	n/a	n/a
19	BACH1	chr4:10185169-10185293	K562	blood:	n/a	n/a
20	BATF	chr4:10182721-10182989	GM12878	blood:	n/a	n/a
21	BCL3	chr4:10191805-10192054	GM12878	blood:	n/a	n/a
22	BCL3	chr4:10206907-10207282	GM12878	blood:	n/a	n/a
23	BCL3	chr4:10182602-10183425	K562	blood:	n/a	chr4:10182894-10182903
24	BCLAF1	chr4:10182260-10183432	K562	blood:	n/a	chr4:10182894-10182903
25	BHLHE40	chr4:10189767-10190685	K562	blood:	n/a	n/a
26	BHLHE40	chr4:10202450-10202808	K562	blood:	n/a	n/a
27	BHLHE40	chr4:10184623-10185411	K562	blood:	n/a	n/a
28	BHLHE40	chr4:10193880-10194273	K562	blood:	n/a	n/a
29	BHLHE40	chr4:10215328-10215399	K562	blood:	n/a	n/a
30	BHLHE40	chr4:10199645-10199963	K562	blood:	n/a	n/a
31	BHLHE40	chr4:10181734-10182063	K562	blood:	n/a	n/a
32	BHLHE40	chr4:10207080-10207159	K562	blood:	n/a	n/a
33	BHLHE40	chr4:10187295-10189374	K562	blood:	n/a	n/a
34	BHLHE40	chr4:10186281-10186687	K562	blood:	n/a	n/a
35	BHLHE40	chr4:10182270-10183899	K562	blood:	n/a	n/a
36	BHLHE40	chr4:10205400-10206307	K562	blood:	n/a	n/a
37	CBX3	chr4:10205085-10205934	K562	blood:	n/a	n/a
38	CBX3	chr4:10199584-10200081	K562	blood:	n/a	n/a
39	CBX3	chr4:10188167-10188696	K562	blood:	n/a	n/a
40	CBX3	chr4:10202326-10202914	K562	blood:	n/a	n/a
41	CBX3	chr4:10187113-10188136	K562	blood:	n/a	n/a
42	CBX3	chr4:10182206-10184538	K562	blood:	n/a	n/a
43	CBX3	chr4:10190221-10190615	K562	blood:	n/a	n/a
44	CBX3	chr4:10182158-10184114	K562	blood:	n/a	n/a
45	CBX3	chr4:10215024-10215411	K562	blood:	n/a	n/a
46	CCNT2	chr4:10182296-10183917	K562	blood:	n/a	n/a
47	CCNT2	chr4:10184361-10184938	K562	blood:	n/a	n/a
48	CCNT2	chr4:10205478-10205881	K562	blood:	n/a	n/a
49	CCNT2	chr4:10181104-10181327	K562	blood:	n/a	n/a
50	CCNT2	chr4:10187286-10188667	K562	blood:	n/a	n/a

No data

(count:90 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr4:10160663..10163901-chr4:10177399..10182680,5	K562	blood:
2	chr4:10109894..10126876-chr4:10164648..10190106,79	K562	blood:
3	chr4:10181386..10184366-chr4:10364568..10366943,2	K562	blood:
4	chr4:10194345..10195861-chr4:10210275..10213111,2	K562	blood:
5	chr4:10186739..10189194-chr4:10403510..10406450,4	K562	blood:
6	chr4:10182452..10185153-chr4:10405566..10407454,2	K562	blood:
7	chr4:10114162..10115900-chr4:10186432..10189186,2	K562	blood:
8	chr4:10185450..10187184-chr4:10401056..10402949,2	K562	blood:
9	chr4:10118276..10120462-chr4:10220218..10222885,3	K562	blood:
10	chr4:10182377..10184143-chr4:10453503..10455042,2	K562	blood:
11	chr4:10210284..10212005-chr4:10213695..10216562,2	K562	blood:
12	chr4:10181292..10183606-chr4:10239969..10241672,2	K562	blood:
13	chr4:10182435..10184114-chr4:10441654..10444481,2	K562	blood:
14	chr4:10206033..10207589-chr4:10220077..10222198,2	K562	blood:
15	chr4:10116403..10118365-chr4:10196419..10198714,2	K562	blood:
16	chr4:10132922..10135214-chr4:10181103..10182859,2	K562	blood:
17	chr4:10203874..10205718-chr4:10217408..10219978,2	K562	blood:
18	chr4:10171114..10171975-chr4:10185300..10186046,2	K562	blood:
19	chr4:10179643..10181436-chr4:10389855..10391388,2	K562	blood:
20	chr4:10210284..10212005-chr4:10213695..10216562,2	K562	blood:
21	chr4:10211963..10215052-chr4:10219787..10222880,4	K562	blood:
22	chr4:10216891..10218631-chr4:10223510..10225830,2	K562	blood:
23	chr4:10194345..10195861-chr4:10210275..10213111,2	K562	blood:
24	chr4:10110816..10113089-chr4:10186992..10189110,2	K562	blood:
25	chr4:10193717..10194647-chr4:10527846..10528670,2	MCF-7	breast:
26	chr4:10112946..10115430-chr4:10181535..10185097,4	K562	blood:
27	chr4:10120021..10122735-chr4:10225048..10229120,3	K562	blood:
28	chr4:10118162..10120785-chr4:10200742..10203933,4	K562	blood:
29	chr4:10181502..10184182-chr4:38665329..38667544,2	K562	blood:
30	chr4:10177971..10181867-chr4:10459708..10464611,4	K562	blood:
31	chr4:10204306..10206166-chr4:10241229..10242983,2	K562	blood:
32	chr4:10175247..10177327-chr4:10228151..10230198,2	K562	blood:
33	chr4:10118560..10120526-chr4:10203986..10206288,3	K562	blood:
34	chr4:10218238..10220165-chr4:10231013..10232714,2	K562	blood:
35	chr4:10234367..10237486-chr4:10239791..10244033,5	K562	blood:
36	chr4:10231830..10233378-chr4:10235064..10237402,2	K562	blood:
37	chr4:10156172..10158401-chr4:10178392..10179954,2	K562	blood:
38	chr4:10206033..10207589-chr4:10220077..10222198,2	K562	blood:
39	chr4:10194015..10194637-chr4:10405680..10406337,2	MCF-7	breast:
40	chr4:10118238..10121011-chr4:10211759..10213607,2	K562	blood:
41	chr4:10182154..10184410-chr4:10456824..10459646,5	K562	blood:
42	chr4:10184632..10187184-chr4:10400763..10402949,2	K562	blood:
43	chr4:10180113..10182537-chr4:10415151..10418343,3	K562	blood:
44	chr4:10187220..10189194-chr4:10403510..10406450,3	K562	blood:
45	chr4:10179915..10182843-chr4:10450700..10452839,2	K562	blood:
46	chr4:10226621..10229156-chr4:10309809..10312332,2	K562	blood:
47	chr4:10216891..10218631-chr4:10223510..10225830,2	K562	blood:
48	chr4:10218238..10220165-chr4:10231013..10232714,2	K562	blood:
49	chr4:10210505..10213622-chr4:10215055..10217234,4	K562	blood:
50	chr4:10179301..10181367-chr4:10408418..10410454,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-WDR1-7	chr4:10201447-10202296	NONHSAT095488

No data

Variant related genes	Relation type
ENSG00000248777	TF binding region
ENSG00000248777	chromatin interactions
ENSG00000109787	chromatin interactions
ENSG00000223086	chromatin interactions
ENSG00000071127	chromatin interactions
ENSG00000231160	chromatin interactions
ENSG00000178163	chromatin interactions
ENSG00000250040	chromatin interactions
ENSG00000271544	chromatin interactions
ENSG00000196355	chromatin interactions

Extended variants
information (count: 3433 )
Associated
traits (count: 56 )

Variant overlapped rSNPs/rCNVs (count:3433 , 50 per page) page: 1 2 3 4 5 6 7 ... 69

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs573363683	chr4:10179299-10179300	Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs551860511	chr4:10179302-10179303	Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs7657551	chr4:10179309-10179310	Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
4	rs542782938	chr4:10179314-10179315	Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs534445390	chr4:10179333-10179334	Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs555552919	chr4:10179348-10179349	Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs573902915	chr4:10179349-10179350	Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs185710333	chr4:10179354-10179355	Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs62285982	chr4:10179374-10179375	Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs56099802	chr4:10179379-10179380	Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs544622086	chr4:10179478-10179479	Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs562787082	chr4:10179519-10179520	Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs114263197	chr4:10179535-10179536	Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs145208772	chr4:10179538-10179539	Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs6449341	chr4:10179542-10179543	Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs535231871	chr4:10179543-10179544	Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs527895203	chr4:10179555-10179556	Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs549513462	chr4:10179557-10179558	Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs567024474	chr4:10179560-10179561	Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs557235872	chr4:10179584-10179585	Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs376636899	chr4:10179615-10179616	Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs549405480	chr4:10179654-10179655	Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs575419478	chr4:10179692-10179693	Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs137876924	chr4:10179702-10179703	Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs142384547	chr4:10179703-10179704	Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs145969544	chr4:10179707-10179708	Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs115718740	chr4:10179710-10179711	Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs375830800	chr4:10179722-10179723	Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs139888373	chr4:10179739-10179740	Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs190621007	chr4:10179762-10179763	Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs544987596	chr4:10179763-10179764	Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs6449342	chr4:10179769-10179770	Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
33	rs556629996	chr4:10179798-10179799	Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs35936546	chr4:10179804-10179805	Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs527347384	chr4:10179811-10179812	Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs35167028	chr4:10179816-10179817	Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs578055717	chr4:10179819-10179820	Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs181737149	chr4:10179825-10179826	Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs548673414	chr4:10179839-10179840	Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs560629523	chr4:10179841-10179842	Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs527939034	chr4:10179857-10179858	Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs372774095	chr4:10179868-10179869	Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs542896299	chr4:10179873-10179874	Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs185712758	chr4:10179874-10179875	Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs59680614	chr4:10179879-10179880	Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs549440612	chr4:10179882-10179883	Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs188607749	chr4:10179909-10179910	Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs529463899	chr4:10179913-10179914	Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs550918419	chr4:10179946-10179947	Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs374802106	chr4:10179947-10179948	Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:56)

Disease	PMID	Source
Colorectal cancer	16272173	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
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
Prostate cancer	18632612	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
Myelofibrosis	22110671	CNVD
Hirschsprung''s Disease	21712996	CNVD
Schizophrenia	22241247	CNVD
Autosomal-dominant microtia	18179897	CNVD
Glioma	17123091	CNVD
Colorectal cancer	20459617	CNVD
Breast cancer	17133270	CNVD
Sezary syndrome	18413736	CNVD
Breast cancer	21858162	CNVD
small cell lung cancer	20016488	CNVD
Neuroblastoma	20406844	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:285 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:10175200-10189000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr4:10176000-10181400	Weak transcription	Primary hematopoietic stem cells	blood
3	chr4:10176200-10183600	Weak transcription	Right Atrium	heart
4	chr4:10176400-10180800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
5	chr4:10176400-10182600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
6	chr4:10176600-10181000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
7	chr4:10176800-10182600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
8	chr4:10177000-10180400	Genic enhancers	K562	blood
9	chr4:10177400-10181600	Weak transcription	Muscle Satellite Cultured Cells	--
10	chr4:10177800-10181200	Weak transcription	HSMM	muscle
11	chr4:10177800-10182400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
12	chr4:10177800-10186400	Weak transcription	Right Ventricle	heart
13	chr4:10178000-10181200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
14	chr4:10178000-10181600	Weak transcription	Osteobl	bone
15	chr4:10178000-10181800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
16	chr4:10178000-10182600	Weak transcription	Placenta	Placenta
17	chr4:10178200-10181400	Weak transcription	HSMMtube	muscle
18	chr4:10178200-10182200	Weak transcription	HMEC	breast
19	chr4:10178800-10180800	Weak transcription	Fetal Heart	heart
20	chr4:10180400-10181000	Enhancers	K562	blood
21	chr4:10180600-10180800	Enhancers	Left Ventricle	heart
22	chr4:10180800-10181400	Weak transcription	Left Ventricle	heart
23	chr4:10180800-10182200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
24	chr4:10180800-10182200	Enhancers	Fetal Heart	heart
25	chr4:10181000-10182200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
26	chr4:10181000-10182800	Flanking Active TSS	K562	blood
27	chr4:10181200-10182600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
28	chr4:10181200-10186800	Enhancers	Primary hematopoietic stem cells short term culture	blood
29	chr4:10181200-10189000	Enhancers	HSMM	muscle
30	chr4:10181400-10182800	Enhancers	Left Ventricle	heart
31	chr4:10181400-10183800	Enhancers	HSMMtube	muscle
32	chr4:10181400-10186600	Enhancers	Primary hematopoietic stem cells	blood
33	chr4:10181600-10182200	Enhancers	Primary neutrophils fromperipheralblood	blood
34	chr4:10181600-10184000	Enhancers	Muscle Satellite Cultured Cells	--
35	chr4:10181600-10184000	Enhancers	Osteobl	bone
36	chr4:10181600-10185000	Enhancers	NHDF-Ad	bronchial
37	chr4:10181600-10186400	Enhancers	Primary monocytes fromperipheralblood	blood
38	chr4:10181800-10182200	Enhancers	Monocytes-CD14+_RO01746	blood
39	chr4:10181800-10182800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
40	chr4:10181800-10182800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
41	chr4:10181800-10183800	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
42	chr4:10181800-10184000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
43	chr4:10181800-10184000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
44	chr4:10182000-10183000	Enhancers	Primary B cells from cord blood	blood
45	chr4:10182200-10182600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
46	chr4:10182200-10183800	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
47	chr4:10182200-10183800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
48	chr4:10182200-10184000	Enhancers	HMEC	breast
49	chr4:10182200-10184000	Enhancers	HUVEC	blood vessel
50	chr4:10182200-10184000	Flanking Active TSS	Monocytes-CD14+_RO01746	blood

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