Variant report

Variant	nsv998973
Chromosome Location	chr4:10178168-10236142
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:712)
CpG islands
(count:0)
Chromatin interactive
region (count:88)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:712 , 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	chr4:10182036-10184108	K562	blood:	n/a	n/a
2	ARID3A	chr4:10202441-10202778	K562	blood:	n/a	n/a
3	ARID3A	chr4:10206944-10207053	HepG2	liver:	n/a	n/a
4	ARID3A	chr4:10206912-10207070	K562	blood:	n/a	n/a
5	ARID3A	chr4:10185222-10185607	K562	blood:	n/a	chr4:10185454-10185470
6	ARID3A	chr4:10188308-10188961	K562	blood:	n/a	n/a
7	ARID3A	chr4:10186847-10188023	K562	blood:	n/a	n/a
8	ATF1	chr4:10187244-10187892	K562	blood:	n/a	n/a
9	ATF1	chr4:10184693-10185042	K562	blood:	n/a	n/a
10	ATF1	chr4:10199601-10200004	K562	blood:	n/a	n/a
11	ATF1	chr4:10188186-10188661	K562	blood:	n/a	n/a
12	ATF1	chr4:10182216-10183403	K562	blood:	n/a	n/a
13	ATF3	chr4:10187352-10187768	K562	blood:	n/a	n/a
14	ATF3	chr4:10182376-10183375	K562	blood:	n/a	n/a
15	BACH1	chr4:10182278-10183266	K562	blood:	n/a	n/a
16	BACH1	chr4:10187292-10187596	K562	blood:	n/a	n/a
17	BACH1	chr4:10185169-10185293	K562	blood:	n/a	n/a
18	BACH1	chr4:10203548-10203807	K562	blood:	n/a	n/a
19	BATF	chr4:10182721-10182989	GM12878	blood:	n/a	n/a
20	BCL3	chr4:10182602-10183425	K562	blood:	n/a	chr4:10182894-10182903
21	BCL3	chr4:10206907-10207282	GM12878	blood:	n/a	n/a
22	BCL3	chr4:10191805-10192054	GM12878	blood:	n/a	n/a
23	BCLAF1	chr4:10182260-10183432	K562	blood:	n/a	chr4:10182894-10182903
24	BHLHE40	chr4:10205400-10206307	K562	blood:	n/a	n/a
25	BHLHE40	chr4:10184623-10185411	K562	blood:	n/a	n/a
26	BHLHE40	chr4:10202450-10202808	K562	blood:	n/a	n/a
27	BHLHE40	chr4:10181734-10182063	K562	blood:	n/a	n/a
28	BHLHE40	chr4:10207080-10207159	K562	blood:	n/a	n/a
29	BHLHE40	chr4:10182270-10183899	K562	blood:	n/a	n/a
30	BHLHE40	chr4:10193880-10194273	K562	blood:	n/a	n/a
31	BHLHE40	chr4:10187295-10189374	K562	blood:	n/a	n/a
32	BHLHE40	chr4:10186281-10186687	K562	blood:	n/a	n/a
33	BHLHE40	chr4:10199645-10199963	K562	blood:	n/a	n/a
34	BHLHE40	chr4:10215328-10215399	K562	blood:	n/a	n/a
35	BHLHE40	chr4:10189767-10190685	K562	blood:	n/a	n/a
36	CBX3	chr4:10187113-10188136	K562	blood:	n/a	n/a
37	CBX3	chr4:10182158-10184114	K562	blood:	n/a	n/a
38	CBX3	chr4:10202326-10202914	K562	blood:	n/a	n/a
39	CBX3	chr4:10190221-10190615	K562	blood:	n/a	n/a
40	CBX3	chr4:10182206-10184538	K562	blood:	n/a	n/a
41	CBX3	chr4:10199584-10200081	K562	blood:	n/a	n/a
42	CBX3	chr4:10205085-10205934	K562	blood:	n/a	n/a
43	CBX3	chr4:10215024-10215411	K562	blood:	n/a	n/a
44	CBX3	chr4:10188167-10188696	K562	blood:	n/a	n/a
45	CCNT2	chr4:10184361-10184938	K562	blood:	n/a	n/a
46	CCNT2	chr4:10205478-10205881	K562	blood:	n/a	n/a
47	CCNT2	chr4:10182296-10183917	K562	blood:	n/a	n/a
48	CCNT2	chr4:10187286-10188667	K562	blood:	n/a	n/a
49	CCNT2	chr4:10181104-10181327	K562	blood:	n/a	n/a
50	CEBPB	chr4:10185418-10186134	K562	blood:	n/a	n/a

No data

(count:88 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr4:10211963..10215052-chr4:10219787..10222880,4	K562	blood:
2	chr4:10182377..10185038-chr4:10453503..10456156,2	K562	blood:
3	chr4:10180539..10184306-chr4:10401076..10403855,3	K562	blood:
4	chr4:10116403..10118365-chr4:10196419..10198714,2	K562	blood:
5	chr4:10181898..10186356-chr4:10317430..10320755,4	K562	blood:
6	chr4:10109894..10126876-chr4:10164648..10190106,79	K562	blood:
7	chr4:10186739..10189194-chr4:10403510..10406450,4	K562	blood:
8	chr4:10226621..10229156-chr4:10309809..10312332,2	K562	blood:
9	chr4:10182716..10185413-chr4:10249318..10252021,2	K562	blood:
10	chr4:10187984..10188890-chr4:10405320..10406071,3	MCF-7	breast:
11	chr4:10194015..10194637-chr4:10405680..10406337,2	MCF-7	breast:
12	chr4:10121764..10123838-chr4:10222085..10224894,2	K562	blood:
13	chr4:10203874..10205718-chr4:10217408..10219978,2	K562	blood:
14	chr4:10231830..10233378-chr4:10235064..10237402,2	K562	blood:
15	chr4:10182377..10184143-chr4:10453503..10455042,2	K562	blood:
16	chr4:10181069..10182933-chr4:10345413..10347984,3	K562	blood:
17	chr4:10116716..10122622-chr4:10178049..10187480,27	K562	blood:
18	chr4:10179301..10181367-chr4:10408418..10410454,2	K562	blood:
19	chr4:10216891..10218631-chr4:10223510..10225830,2	K562	blood:
20	chr4:10216891..10218631-chr4:10223510..10225830,2	K562	blood:
21	chr4:10193717..10194647-chr4:10527846..10528670,2	MCF-7	breast:
22	chr4:10175247..10177327-chr4:10228151..10230198,2	K562	blood:
23	chr4:10118560..10120526-chr4:10203986..10206288,3	K562	blood:
24	chr4:10206033..10207589-chr4:10220077..10222198,2	K562	blood:
25	chr4:10199615..10202739-chr4:10203951..10206560,3	K562	blood:
26	chr4:10210284..10212005-chr4:10213695..10216562,2	K562	blood:
27	chr4:10124578..10127302-chr4:10186119..10188725,2	K562	blood:
28	chr4:10187220..10189194-chr4:10403510..10406450,3	K562	blood:
29	chr4:10231830..10233378-chr4:10235064..10237402,2	K562	blood:
30	chr4:10118162..10120785-chr4:10200742..10203933,4	K562	blood:
31	chr4:10211963..10215052-chr4:10219787..10222880,4	K562	blood:
32	chr4:10112946..10115430-chr4:10181535..10185097,4	K562	blood:
33	chr4:10180991..10182787-chr4:10327240..10329402,2	K562	blood:
34	chr4:10175466..10178390-chr4:10458313..10460581,2	K562	blood:
35	chr4:10234367..10237486-chr4:10239791..10244033,5	K562	blood:
36	chr4:10218238..10220165-chr4:10231013..10232714,2	K562	blood:
37	chr4:10185102..10187379-chr4:10256972..10258730,2	K562	blood:
38	chr4:10218238..10220165-chr4:10231013..10232714,2	K562	blood:
39	chr4:10119371..10120949-chr4:10187732..10190413,2	K562	blood:
40	chr4:10179915..10182843-chr4:10450700..10452839,2	K562	blood:
41	chr4:10185450..10187184-chr4:10401056..10402949,2	K562	blood:
42	chr4:10120021..10122735-chr4:10225048..10229120,3	K562	blood:
43	chr4:10171114..10171975-chr4:10185300..10186046,2	K562	blood:
44	chr4:10181386..10184366-chr4:10364568..10366943,2	K562	blood:
45	chr4:10210505..10213622-chr4:10215055..10217234,4	K562	blood:
46	chr4:10137227..10139603-chr4:10183343..10185587,3	K562	blood:
47	chr4:10119416..10121988-chr4:10218168..10219976,2	K562	blood:
48	chr4:10210505..10213622-chr4:10215055..10217234,4	K562	blood:
49	chr4:10181802..10184742-chr4:10401642..10403855,2	K562	blood:
50	chr4:10179643..10181436-chr4:10389855..10391388,2	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
ENSG00000071127	chromatin interactions
ENSG00000109787	chromatin interactions
ENSG00000271544	chromatin interactions
ENSG00000250040	chromatin interactions
ENSG00000178163	chromatin interactions
ENSG00000223086	chromatin interactions
ENSG00000231160	chromatin interactions
ENSG00000196355	chromatin interactions

Extended variants
information (count: 3303 )
Associated
traits (count: 56 )

Variant overlapped rSNPs/rCNVs (count:3303 , 50 per page) page: 1 2 3 4 5 6 7 ... 67

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs17385872	chr4:10178168-10178169	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs116189390	chr4:10178169-10178170	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs145403431	chr4:10178179-10178180	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs16894579	chr4:10178217-10178218	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
5	rs73089941	chr4:10178228-10178229	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs73089942	chr4:10178235-10178236	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs536054207	chr4:10178246-10178247	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs116117572	chr4:10178255-10178256	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs575455778	chr4:10178256-10178257	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs78675759	chr4:10178261-10178262	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs557824282	chr4:10178320-10178321	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs572778219	chr4:10178325-10178326	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs539820094	chr4:10178329-10178330	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs76677388	chr4:10178331-10178332	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs148800041	chr4:10178335-10178336	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs116778774	chr4:10178338-10178339	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs375282436	chr4:10178345-10178346	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs562340901	chr4:10178357-10178358	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs142248387	chr4:10178365-10178366	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs79815151	chr4:10178375-10178376	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs77735513	chr4:10178376-10178377	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs76457587	chr4:10178400-10178401	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs62285981	chr4:10178421-10178422	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs546634764	chr4:10178466-10178467	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs568737012	chr4:10178489-10178490	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs535768138	chr4:10178522-10178523	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs10033955	chr4:10178556-10178557	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
28	rs573282378	chr4:10178564-10178565	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs147882637	chr4:10178586-10178587	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs9291661	chr4:10178622-10178623	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
31	rs141613134	chr4:10178624-10178625	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs76174358	chr4:10178654-10178655	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs555016674	chr4:10178666-10178667	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs573925534	chr4:10178677-10178678	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs544086117	chr4:10178689-10178690	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs113149464	chr4:10178706-10178707	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs568149257	chr4:10178720-10178721	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs369946460	chr4:10178726-10178727	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs114361276	chr4:10178729-10178730	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs147058049	chr4:10178770-10178771	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs529159103	chr4:10178778-10178779	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs370638423	chr4:10178785-10178786	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs79380179	chr4:10178800-10178801	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs547015951	chr4:10178801-10178802	Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs550896914	chr4:10178814-10178815	Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs562316638	chr4:10178818-10178819	Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs192987909	chr4:10178831-10178832	Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs529628616	chr4:10178832-10178833	Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs182854303	chr4:10178838-10178839	Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs569544939	chr4:10178872-10178873	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:289 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:10172800-10178400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
2	chr4:10174000-10178200	Enhancers	HSMMtube	muscle
3	chr4:10175200-10189000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr4:10176000-10178800	Enhancers	Fetal Heart	heart
5	chr4:10176000-10181400	Weak transcription	Primary hematopoietic stem cells	blood
6	chr4:10176200-10183600	Weak transcription	Right Atrium	heart
7	chr4:10176400-10180800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
8	chr4:10176400-10182600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
9	chr4:10176600-10181000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
10	chr4:10176800-10182600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
11	chr4:10177000-10180400	Genic enhancers	K562	blood
12	chr4:10177400-10181600	Weak transcription	Muscle Satellite Cultured Cells	--
13	chr4:10177600-10178200	Enhancers	HMEC	breast
14	chr4:10177600-10178200	Enhancers	NHEK	skin
15	chr4:10177800-10178600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
16	chr4:10177800-10181200	Weak transcription	HSMM	muscle
17	chr4:10177800-10182400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
18	chr4:10177800-10186400	Weak transcription	Right Ventricle	heart
19	chr4:10178000-10181200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
20	chr4:10178000-10181600	Weak transcription	Osteobl	bone
21	chr4:10178000-10181800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
22	chr4:10178000-10182600	Weak transcription	Placenta	Placenta
23	chr4:10178200-10181400	Weak transcription	HSMMtube	muscle
24	chr4:10178200-10182200	Weak transcription	HMEC	breast
25	chr4:10178800-10180800	Weak transcription	Fetal Heart	heart
26	chr4:10180400-10181000	Enhancers	K562	blood
27	chr4:10180600-10180800	Enhancers	Left Ventricle	heart
28	chr4:10180800-10181400	Weak transcription	Left Ventricle	heart
29	chr4:10180800-10182200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
30	chr4:10180800-10182200	Enhancers	Fetal Heart	heart
31	chr4:10181000-10182200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
32	chr4:10181000-10182800	Flanking Active TSS	K562	blood
33	chr4:10181200-10182600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
34	chr4:10181200-10186800	Enhancers	Primary hematopoietic stem cells short term culture	blood
35	chr4:10181200-10189000	Enhancers	HSMM	muscle
36	chr4:10181400-10182800	Enhancers	Left Ventricle	heart
37	chr4:10181400-10183800	Enhancers	HSMMtube	muscle
38	chr4:10181400-10186600	Enhancers	Primary hematopoietic stem cells	blood
39	chr4:10181600-10182200	Enhancers	Primary neutrophils fromperipheralblood	blood
40	chr4:10181600-10184000	Enhancers	Muscle Satellite Cultured Cells	--
41	chr4:10181600-10184000	Enhancers	Osteobl	bone
42	chr4:10181600-10185000	Enhancers	NHDF-Ad	bronchial
43	chr4:10181600-10186400	Enhancers	Primary monocytes fromperipheralblood	blood
44	chr4:10181800-10182200	Enhancers	Monocytes-CD14+_RO01746	blood
45	chr4:10181800-10182800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
46	chr4:10181800-10182800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
47	chr4:10181800-10183800	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
48	chr4:10181800-10184000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
49	chr4:10181800-10184000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
50	chr4:10182000-10183000	Enhancers	Primary B cells from cord blood	blood

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