Variant report

Variant	nsv1000149
Chromosome Location	chr4:10183420-10231486
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:634)
CpG islands
(count:0)
Chromatin interactive
region (count:73)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:634 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:10206944-10207053	HepG2	liver:	n/a	n/a
2	ARID3A	chr4:10182036-10184108	K562	blood:	n/a	n/a
3	ARID3A	chr4:10206912-10207070	K562	blood:	n/a	n/a
4	ARID3A	chr4:10185222-10185607	K562	blood:	n/a	chr4:10185454-10185470
5	ARID3A	chr4:10188308-10188961	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	chr4:10199601-10200004	K562	blood:	n/a	n/a
11	ATF1	chr4:10184693-10185042	K562	blood:	n/a	n/a
12	ATF3	chr4:10187352-10187768	K562	blood:	n/a	n/a
13	BACH1	chr4:10185169-10185293	K562	blood:	n/a	n/a
14	BACH1	chr4:10203548-10203807	K562	blood:	n/a	n/a
15	BACH1	chr4:10187292-10187596	K562	blood:	n/a	n/a
16	BCL3	chr4:10182602-10183425	K562	blood:	n/a	chr4:10182894-10182903
17	BCL3	chr4:10206907-10207282	GM12878	blood:	n/a	n/a
18	BCL3	chr4:10191805-10192054	GM12878	blood:	n/a	n/a
19	BCLAF1	chr4:10182260-10183432	K562	blood:	n/a	chr4:10182894-10182903
20	BHLHE40	chr4:10193880-10194273	K562	blood:	n/a	n/a
21	BHLHE40	chr4:10187295-10189374	K562	blood:	n/a	n/a
22	BHLHE40	chr4:10205400-10206307	K562	blood:	n/a	n/a
23	BHLHE40	chr4:10207080-10207159	K562	blood:	n/a	n/a
24	BHLHE40	chr4:10182270-10183899	K562	blood:	n/a	n/a
25	BHLHE40	chr4:10199645-10199963	K562	blood:	n/a	n/a
26	BHLHE40	chr4:10189767-10190685	K562	blood:	n/a	n/a
27	BHLHE40	chr4:10215328-10215399	K562	blood:	n/a	n/a
28	BHLHE40	chr4:10184623-10185411	K562	blood:	n/a	n/a
29	BHLHE40	chr4:10202450-10202808	K562	blood:	n/a	n/a
30	BHLHE40	chr4:10186281-10186687	K562	blood:	n/a	n/a
31	CBX3	chr4:10199584-10200081	K562	blood:	n/a	n/a
32	CBX3	chr4:10188167-10188696	K562	blood:	n/a	n/a
33	CBX3	chr4:10202326-10202914	K562	blood:	n/a	n/a
34	CBX3	chr4:10205085-10205934	K562	blood:	n/a	n/a
35	CBX3	chr4:10187113-10188136	K562	blood:	n/a	n/a
36	CBX3	chr4:10190221-10190615	K562	blood:	n/a	n/a
37	CBX3	chr4:10182158-10184114	K562	blood:	n/a	n/a
38	CBX3	chr4:10182206-10184538	K562	blood:	n/a	n/a
39	CBX3	chr4:10215024-10215411	K562	blood:	n/a	n/a
40	CCNT2	chr4:10184361-10184938	K562	blood:	n/a	n/a
41	CCNT2	chr4:10205478-10205881	K562	blood:	n/a	n/a
42	CCNT2	chr4:10187286-10188667	K562	blood:	n/a	n/a
43	CCNT2	chr4:10182296-10183917	K562	blood:	n/a	n/a
44	CEBPB	chr4:10204959-10205937	K562	blood:	n/a	chr4:10205836-10205844 chr4:10205110-10205121
45	CEBPB	chr4:10207049-10207196	HepG2	liver:	n/a	n/a
46	CEBPB	chr4:10195735-10195985	A549	lung:	n/a	n/a
47	CEBPB	chr4:10183343-10183757	IMR90	lung:	n/a	n/a
48	CEBPB	chr4:10204944-10205268	HepG2	liver:	n/a	chr4:10205110-10205121
49	CEBPB	chr4:10195806-10195900	HepG2	liver:	n/a	n/a
50	CEBPB	chr4:10185605-10186142	IMR90	lung:	n/a	n/a

No data

(count:73 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr4:10182154..10184410-chr4:10456824..10459646,5	K562	blood:
2	chr4:10210284..10212005-chr4:10213695..10216562,2	K562	blood:
3	chr4:10181799..10184639-chr4:10262185..10264664,2	K562	blood:
4	chr4:10186685..10189037-chr4:10459555..10461188,2	K562	blood:
5	chr4:10117656..10120785-chr4:10200069..10203011,5	K562	blood:
6	chr4:10226621..10229156-chr4:10309809..10312332,2	K562	blood:
7	chr4:10120021..10122735-chr4:10225048..10229120,3	K562	blood:
8	chr4:10118276..10120462-chr4:10220218..10222885,3	K562	blood:
9	chr4:10109894..10126876-chr4:10164648..10190106,79	K562	blood:
10	chr4:10182716..10185413-chr4:10249318..10252021,2	K562	blood:
11	chr4:10210505..10213622-chr4:10215055..10217234,4	K562	blood:
12	chr4:10116403..10118365-chr4:10196419..10198714,2	K562	blood:
13	chr4:10207125..10208799-chr4:10284967..10286577,2	K562	blood:
14	chr4:10210505..10213622-chr4:10215055..10217234,4	K562	blood:
15	chr4:10114162..10115900-chr4:10186432..10189186,2	K562	blood:
16	chr4:10210284..10212005-chr4:10213695..10216562,2	K562	blood:
17	chr4:10185102..10187379-chr4:10256972..10258730,2	K562	blood:
18	chr4:10193717..10194647-chr4:10527846..10528670,2	MCF-7	breast:
19	chr4:10118162..10120785-chr4:10200742..10203933,4	K562	blood:
20	chr4:10119416..10121988-chr4:10218168..10219976,2	K562	blood:
21	chr4:10202106..10207051-chr4:10207371..10210794,7	K562	blood:
22	chr4:10204306..10206166-chr4:10241229..10242983,2	K562	blood:
23	chr4:10119371..10120949-chr4:10187732..10190413,2	K562	blood:
24	chr4:10211963..10215052-chr4:10219787..10222880,4	K562	blood:
25	chr4:10171114..10171975-chr4:10185300..10186046,2	K562	blood:
26	chr4:10118238..10121011-chr4:10211759..10213607,2	K562	blood:
27	chr4:10184632..10187184-chr4:10400763..10402949,2	K562	blood:
28	chr4:10182452..10185153-chr4:10405566..10407454,2	K562	blood:
29	chr4:10181502..10184182-chr4:38665329..38667544,2	K562	blood:
30	chr4:10114665..10116599-chr4:10227448..10229354,2	K562	blood:
31	chr4:10118560..10120526-chr4:10203986..10206288,3	K562	blood:
32	chr4:10186739..10189194-chr4:10403510..10406450,4	K562	blood:
33	chr4:10137227..10139603-chr4:10183343..10185587,3	K562	blood:
34	chr4:10218238..10220165-chr4:10231013..10232714,2	K562	blood:
35	chr4:10211963..10215052-chr4:10219787..10222880,4	K562	blood:
36	chr4:10181386..10184366-chr4:10364568..10366943,2	K562	blood:
37	chr4:10203874..10205718-chr4:10217408..10219978,2	K562	blood:
38	chr4:10182377..10184143-chr4:10453503..10455042,2	K562	blood:
39	chr4:10194345..10195861-chr4:10210275..10213111,2	K562	blood:
40	chr4:10182073..10186416-chr4:10457121..10461088,7	K562	blood:
41	chr4:10186571..10188279-chr4:10316070..10319056,2	K562	blood:
42	chr4:10206033..10207589-chr4:10220077..10222198,2	K562	blood:
43	chr4:10112946..10115430-chr4:10181535..10185097,4	K562	blood:
44	chr4:10180539..10184306-chr4:10401076..10403855,3	K562	blood:
45	chr4:10187220..10189194-chr4:10403510..10406450,3	K562	blood:
46	chr4:10181898..10186356-chr4:10317430..10320755,4	K562	blood:
47	chr4:10181292..10183606-chr4:10239969..10241672,2	K562	blood:
48	chr4:10180991..10184001-chr4:10327240..10329402,3	K562	blood:
49	chr4:10182491..10184302-chr4:10237283..10239761,2	K562	blood:
50	chr4:10181802..10184742-chr4:10401642..10403855,2	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
ENSG00000109787	chromatin interactions
ENSG00000248777	chromatin interactions
ENSG00000196355	chromatin interactions
ENSG00000178163	chromatin interactions
ENSG00000071127	chromatin interactions
ENSG00000223086	chromatin interactions
ENSG00000231160	chromatin interactions
ENSG00000250040	chromatin interactions

Extended variants
information (count: 2712 )
Associated
traits (count: 56 )

Variant overlapped rSNPs/rCNVs (count:2712 , 50 per page) page: 1 2 3 4 5 6 7 ... 55

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10489081	chr4:10183420-10183421	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs561135018	chr4:10183433-10183434	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
3	rs182000061	chr4:10183437-10183438	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
4	rs186387476	chr4:10183444-10183445	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
5	rs536148418	chr4:10183453-10183454	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
6	rs554094351	chr4:10183456-10183457	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
7	rs564803115	chr4:10183465-10183466	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
8	rs532152588	chr4:10183480-10183481	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
9	rs117056332	chr4:10183508-10183509	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
10	rs559688777	chr4:10183509-10183510	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
11	rs530014537	chr4:10183521-10183522	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
12	rs887730	chr4:10183566-10183567	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs115724407	chr4:10183590-10183591	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
14	rs887729	chr4:10183611-10183612	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
15	rs114918688	chr4:10183622-10183623	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
16	rs80168802	chr4:10183640-10183641	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
17	rs190791374	chr4:10183687-10183688	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
18	rs183028796	chr4:10183691-10183692	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
19	rs553356592	chr4:10183702-10183703	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
20	rs566069927	chr4:10183709-10183710	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
21	rs6812510	chr4:10183725-10183726	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs554772621	chr4:10183728-10183729	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
23	rs148197812	chr4:10183731-10183732	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
24	rs187991704	chr4:10183759-10183760	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
25	rs558631387	chr4:10183764-10183765	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
26	rs191265325	chr4:10183774-10183775	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
27	rs182633285	chr4:10183789-10183790	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
28	rs559382838	chr4:10183795-10183796	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
29	rs887728	chr4:10183798-10183799	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
30	rs150317611	chr4:10183815-10183816	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
31	rs887727	chr4:10183819-10183820	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
32	rs187763373	chr4:10183827-10183828	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
33	rs138006189	chr4:10183832-10183833	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
34	rs571756383	chr4:10183857-10183858	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
35	rs887726	chr4:10183869-10183870	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs191197556	chr4:10183891-10183892	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
37	rs184828662	chr4:10183892-10183893	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
38	rs887725	chr4:10183895-10183896	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
39	rs554860622	chr4:10183896-10183897	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
40	rs570216065	chr4:10183945-10183946	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
41	rs143199986	chr4:10183946-10183947	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
42	rs147512266	chr4:10183947-10183948	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
43	rs527950124	chr4:10183962-10183963	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
44	rs16894728	chr4:10183982-10183983	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
45	rs553034169	chr4:10184001-10184002	Weak transcription Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
46	rs372653943	chr4:10184002-10184003	Weak transcription Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
47	rs574499434	chr4:10184004-10184005	Weak transcription Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
48	rs549697304	chr4:10184010-10184011	Weak transcription Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
49	rs551576814	chr4:10184025-10184026	Weak transcription Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
50	rs187734231	chr4:10184048-10184049	Weak transcription Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	6 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:222 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:10175200-10189000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr4:10176200-10183600	Weak transcription	Right Atrium	heart
3	chr4:10177800-10186400	Weak transcription	Right Ventricle	heart
4	chr4:10181200-10186800	Enhancers	Primary hematopoietic stem cells short term culture	blood
5	chr4:10181200-10189000	Enhancers	HSMM	muscle
6	chr4:10181400-10183800	Enhancers	HSMMtube	muscle
7	chr4:10181400-10186600	Enhancers	Primary hematopoietic stem cells	blood
8	chr4:10181600-10184000	Enhancers	Muscle Satellite Cultured Cells	--
9	chr4:10181600-10184000	Enhancers	Osteobl	bone
10	chr4:10181600-10185000	Enhancers	NHDF-Ad	bronchial
11	chr4:10181600-10186400	Enhancers	Primary monocytes fromperipheralblood	blood
12	chr4:10181800-10183800	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
13	chr4:10181800-10184000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
14	chr4:10181800-10184000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
15	chr4:10182200-10183800	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
16	chr4:10182200-10183800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
17	chr4:10182200-10184000	Enhancers	HMEC	breast
18	chr4:10182200-10184000	Enhancers	HUVEC	blood vessel
19	chr4:10182200-10184000	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
20	chr4:10182200-10186400	Weak transcription	Fetal Heart	heart
21	chr4:10182400-10184000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
22	chr4:10182400-10184000	Enhancers	NHEK	skin
23	chr4:10182400-10185200	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
24	chr4:10182600-10183600	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
25	chr4:10182600-10183800	Enhancers	Placenta	Placenta
26	chr4:10182600-10184000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
27	chr4:10182600-10184000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
28	chr4:10182600-10184000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
29	chr4:10182600-10186400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
30	chr4:10182800-10187400	Weak transcription	Left Ventricle	heart
31	chr4:10183200-10184000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
32	chr4:10183200-10184000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
33	chr4:10183200-10184000	Flanking Active TSS	K562	blood
34	chr4:10183200-10184200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
35	chr4:10183200-10184400	Weak transcription	Primary T cells from cord blood	blood
36	chr4:10183200-10184400	Weak transcription	Primary T helper cells PMA-I stimulated	--
37	chr4:10183200-10184600	Enhancers	Primary B cells from cord blood	blood
38	chr4:10183200-10184600	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
39	chr4:10183200-10185000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
40	chr4:10183200-10185000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
41	chr4:10183400-10184600	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
42	chr4:10183400-10184600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
43	chr4:10183400-10185600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
44	chr4:10183400-10187200	Weak transcription	Sigmoid Colon	Sigmoid Colon
45	chr4:10183400-10190600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
46	chr4:10183600-10184000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
47	chr4:10183600-10184000	Enhancers	Lung	lung
48	chr4:10183600-10184000	Enhancers	Right Atrium	heart
49	chr4:10183800-10185800	Weak transcription	HSMMtube	muscle
50	chr4:10183800-10186400	Enhancers	Primary neutrophils fromperipheralblood	blood

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