Variant report

Variant	esv1817634
Chromosome Location	chr4:10186760-10246264
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:566)
CpG islands
(count:0)
Chromatin interactive
region (count:69)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:566 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:10186847-10188023	K562	blood:	n/a	n/a
2	ARID3A	chr4:10206944-10207053	HepG2	liver:	n/a	n/a
3	ARID3A	chr4:10202441-10202778	K562	blood:	n/a	n/a
4	ARID3A	chr4:10206912-10207070	K562	blood:	n/a	n/a
5	ARID3A	chr4:10242016-10242400	K562	blood:	n/a	n/a
6	ARID3A	chr4:10188308-10188961	K562	blood:	n/a	n/a
7	ARID3A	chr4:10241023-10241142	K562	blood:	n/a	n/a
8	ATF1	chr4:10187244-10187892	K562	blood:	n/a	n/a
9	ATF1	chr4:10188186-10188661	K562	blood:	n/a	n/a
10	ATF1	chr4:10199601-10200004	K562	blood:	n/a	n/a
11	ATF1	chr4:10241521-10242349	K562	blood:	n/a	n/a
12	ATF3	chr4:10187352-10187768	K562	blood:	n/a	n/a
13	ATF3	chr4:10241484-10241931	K562	blood:	n/a	chr4:10241683-10241696
14	BACH1	chr4:10187292-10187596	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	BCL3	chr4:10191805-10192054	GM12878	blood:	n/a	n/a
18	BCL3	chr4:10206907-10207282	GM12878	blood:	n/a	n/a
19	BHLHE40	chr4:10189767-10190685	K562	blood:	n/a	n/a
20	BHLHE40	chr4:10239996-10240058	K562	blood:	n/a	n/a
21	BHLHE40	chr4:10205400-10206307	K562	blood:	n/a	n/a
22	BHLHE40	chr4:10207080-10207159	K562	blood:	n/a	n/a
23	BHLHE40	chr4:10241629-10242291	K562	blood:	n/a	n/a
24	BHLHE40	chr4:10202450-10202808	K562	blood:	n/a	n/a
25	BHLHE40	chr4:10187295-10189374	K562	blood:	n/a	n/a
26	BHLHE40	chr4:10193880-10194273	K562	blood:	n/a	n/a
27	BHLHE40	chr4:10215328-10215399	K562	blood:	n/a	n/a
28	BHLHE40	chr4:10199645-10199963	K562	blood:	n/a	n/a
29	CBX3	chr4:10199584-10200081	K562	blood:	n/a	n/a
30	CBX3	chr4:10215024-10215411	K562	blood:	n/a	n/a
31	CBX3	chr4:10190221-10190615	K562	blood:	n/a	n/a
32	CBX3	chr4:10187113-10188136	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	chr4:10188167-10188696	K562	blood:	n/a	n/a
36	CCNT2	chr4:10205478-10205881	K562	blood:	n/a	n/a
37	CCNT2	chr4:10241954-10242255	K562	blood:	n/a	n/a
38	CCNT2	chr4:10187286-10188667	K562	blood:	n/a	n/a
39	CEBPB	chr4:10187475-10188067	K562	blood:	n/a	n/a
40	CEBPB	chr4:10195806-10195900	HepG2	liver:	n/a	n/a
41	CEBPB	chr4:10202340-10202672	K562	blood:	n/a	n/a
42	CEBPB	chr4:10204944-10205268	HepG2	liver:	n/a	chr4:10205110-10205121
43	CEBPB	chr4:10204959-10205937	K562	blood:	n/a	chr4:10205836-10205844 chr4:10205110-10205121
44	CEBPB	chr4:10187279-10187809	K562	blood:	n/a	n/a
45	CEBPB	chr4:10195735-10195985	A549	lung:	n/a	n/a
46	CEBPB	chr4:10205485-10205827	K562	blood:	n/a	n/a
47	CEBPB	chr4:10207049-10207196	HepG2	liver:	n/a	n/a
48	CEBPD	chr4:10187228-10187887	K562	blood:	n/a	n/a
49	CEBPD	chr4:10241894-10242416	K562	blood:	n/a	n/a
50	CEBPD	chr4:10241866-10242444	K562	blood:	n/a	n/a

No data

(count:69 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr4:10118238..10121011-chr4:10211759..10213607,2	K562	blood:
2	chr4:10199615..10202739-chr4:10203951..10206560,3	K562	blood:
3	chr4:10110816..10113089-chr4:10186992..10189110,2	K562	blood:
4	chr4:10210284..10212005-chr4:10213695..10216562,2	K562	blood:
5	chr4:10202106..10207051-chr4:10207371..10210794,7	K562	blood:
6	chr4:10203874..10205718-chr4:10217408..10219978,2	K562	blood:
7	chr4:10185450..10187184-chr4:10401056..10402949,2	K562	blood:
8	chr4:10184632..10187184-chr4:10400763..10402949,2	K562	blood:
9	chr4:10119371..10120949-chr4:10187732..10190413,2	K562	blood:
10	chr4:10204306..10206166-chr4:10241229..10242983,2	K562	blood:
11	chr4:10226621..10229156-chr4:10309809..10312332,2	K562	blood:
12	chr4:10231830..10233378-chr4:10235064..10237402,2	K562	blood:
13	chr4:10116716..10122622-chr4:10178049..10187480,27	K562	blood:
14	chr4:10119817..10122040-chr4:10243013..10245878,2	K562	blood:
15	chr4:10211963..10215052-chr4:10219787..10222880,4	K562	blood:
16	chr4:10216891..10218631-chr4:10223510..10225830,2	K562	blood:
17	chr4:10187984..10188890-chr4:10405320..10406071,3	MCF-7	breast:
18	chr4:10174527..10176209-chr4:10240126..10241692,2	K562	blood:
19	chr4:10216891..10218631-chr4:10223510..10225830,2	K562	blood:
20	chr4:10203874..10205718-chr4:10217408..10219978,2	K562	blood:
21	chr4:10236259..10238046-chr4:10240029..10241603,2	K562	blood:
22	chr4:10207125..10208799-chr4:10284967..10286577,2	K562	blood:
23	chr4:10118560..10120526-chr4:10203986..10206288,3	K562	blood:
24	chr4:10175247..10177327-chr4:10228151..10230198,2	K562	blood:
25	chr4:10186739..10189194-chr4:10403510..10406450,4	K562	blood:
26	chr4:10186685..10189037-chr4:10459555..10461188,2	K562	blood:
27	chr4:10234367..10237486-chr4:10239791..10244033,5	K562	blood:
28	chr4:10239005..10240530-chr4:10240711..10243694,2	K562	blood:
29	chr4:10218238..10220165-chr4:10231013..10232714,2	K562	blood:
30	chr4:10210284..10212005-chr4:10213695..10216562,2	K562	blood:
31	chr4:10194015..10194637-chr4:10405680..10406337,2	MCF-7	breast:
32	chr4:10200377..10202730-chr4:10225143..10227711,2	K562	blood:
33	chr4:10204306..10206166-chr4:10241229..10242983,2	K562	blood:
34	chr4:10194345..10195861-chr4:10210275..10213111,2	K562	blood:
35	chr4:10118276..10120462-chr4:10220218..10222885,3	K562	blood:
36	chr4:10187220..10189194-chr4:10403510..10406450,3	K562	blood:
37	chr4:10244335..10247662-chr4:10255817..10258798,3	K562	blood:
38	chr4:10185102..10187379-chr4:10256972..10258730,2	K562	blood:
39	chr4:10186571..10188279-chr4:10316070..10319056,2	K562	blood:
40	chr4:10183994..10188822-chr4:10326557..10329780,4	K562	blood:
41	chr4:10240628..10243680-chr4:10247596..10249776,3	K562	blood:
42	chr4:10124578..10127302-chr4:10186119..10188725,2	K562	blood:
43	chr4:10210505..10213622-chr4:10215055..10217234,4	K562	blood:
44	chr4:10117656..10120785-chr4:10200069..10203011,5	K562	blood:
45	chr4:10194345..10195861-chr4:10210275..10213111,2	K562	blood:
46	chr4:10234367..10236533-chr4:10242137..10244033,2	K562	blood:
47	chr4:10118162..10120785-chr4:10200742..10203933,4	K562	blood:
48	chr4:10210505..10213622-chr4:10215055..10217234,4	K562	blood:
49	chr4:10119416..10121988-chr4:10218168..10219976,2	K562	blood:
50	chr4:10234367..10236533-chr4:10242137..10244033,2	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
ENSG00000271544	TF binding region
ENSG00000223086	chromatin interactions
ENSG00000248777	chromatin interactions
ENSG00000271544	chromatin interactions
ENSG00000250040	chromatin interactions
ENSG00000071127	chromatin interactions

Extended variants
information (count: 3326 )
Associated
traits (count: 56 )

Variant overlapped rSNPs/rCNVs (count:3326 , 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	rs530699699	chr4:10186761-10186762	Enhancers Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
2	rs575257301	chr4:10186764-10186765	Enhancers Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs145125901	chr4:10186765-10186766	Enhancers Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs570430066	chr4:10186779-10186780	Enhancers Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs531225275	chr4:10186795-10186796	Enhancers Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs11722345	chr4:10186799-10186800	Enhancers Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
7	rs564997770	chr4:10186804-10186805	Enhancers Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs374926126	chr4:10186842-10186843	Enhancers Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs377429453	chr4:10186843-10186844	Enhancers Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs547383065	chr4:10186845-10186846	Enhancers Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs144903738	chr4:10186863-10186864	Enhancers Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs536530132	chr4:10186875-10186876	Enhancers Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs548793561	chr4:10186887-10186888	Enhancers Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs570177169	chr4:10186901-10186902	Enhancers Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs537618374	chr4:10186905-10186906	Enhancers Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs560243958	chr4:10186921-10186922	Enhancers Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs535550099	chr4:10186939-10186940	Enhancers Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs57247752	chr4:10186956-10186957	Enhancers Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs576968611	chr4:10186958-10186959	Enhancers Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs534654406	chr4:10186959-10186960	Enhancers Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs552997414	chr4:10186982-10186983	Enhancers Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs574702666	chr4:10187010-10187011	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs554814843	chr4:10187034-10187035	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs549416016	chr4:10187070-10187071	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs567858336	chr4:10187074-10187075	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs545297280	chr4:10187078-10187079	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs190378688	chr4:10187081-10187082	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs535290959	chr4:10187088-10187089	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs565083083	chr4:10187103-10187104	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs181700632	chr4:10187110-10187111	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs62285984	chr4:10187114-10187115	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
32	rs114358761	chr4:10187121-10187122	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs530077977	chr4:10187141-10187142	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs548618627	chr4:10187158-10187159	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs116361751	chr4:10187168-10187169	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs531016497	chr4:10187169-10187170	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs58099252	chr4:10187181-10187182	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs570603687	chr4:10187188-10187189	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs186758514	chr4:10187191-10187192	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs547598889	chr4:10187206-10187207	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs142024104	chr4:10187238-10187239	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs13118647	chr4:10187241-10187242	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs371405979	chr4:10187245-10187246	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs556978116	chr4:10187251-10187252	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs145852028	chr4:10187254-10187255	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs4697960	chr4:10187263-10187264	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
47	rs79708682	chr4:10187267-10187268	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs576953529	chr4:10187286-10187287	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs147810917	chr4:10187288-10187289	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs559388621	chr4:10187289-10187290	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	3 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:165 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:10175200-10189000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr4:10181200-10186800	Enhancers	Primary hematopoietic stem cells short term culture	blood
3	chr4:10181200-10189000	Enhancers	HSMM	muscle
4	chr4:10182800-10187400	Weak transcription	Left Ventricle	heart
5	chr4:10183400-10187200	Weak transcription	Sigmoid Colon	Sigmoid Colon
6	chr4:10183400-10190600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
7	chr4:10184000-10187000	Transcr. at gene 5' and 3'	K562	blood
8	chr4:10184000-10187400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
9	chr4:10184000-10187400	Weak transcription	HUVEC	blood vessel
10	chr4:10184000-10189200	Weak transcription	Right Atrium	heart
11	chr4:10184000-10190600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
12	chr4:10184000-10194200	Weak transcription	HMEC	breast
13	chr4:10185000-10187200	Weak transcription	NHDF-Ad	bronchial
14	chr4:10185800-10187800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
15	chr4:10186200-10186800	Enhancers	Lung	lung
16	chr4:10186200-10187400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
17	chr4:10186200-10187400	Weak transcription	HSMMtube	muscle
18	chr4:10186200-10187800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
19	chr4:10186400-10187400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
20	chr4:10186400-10187600	Weak transcription	Muscle Satellite Cultured Cells	--
21	chr4:10186400-10187600	Weak transcription	Osteobl	bone
22	chr4:10186400-10187800	Enhancers	Fetal Heart	heart
23	chr4:10186600-10187000	Weak transcription	Right Ventricle	heart
24	chr4:10186800-10187400	Weak transcription	Lung	lung
25	chr4:10187000-10188200	Flanking Active TSS	K562	blood
26	chr4:10187000-10188600	Enhancers	Right Ventricle	heart
27	chr4:10187200-10188400	Enhancers	Sigmoid Colon	Sigmoid Colon
28	chr4:10187200-10188400	Enhancers	NHDF-Ad	bronchial
29	chr4:10187200-10188600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
30	chr4:10187400-10187600	Enhancers	Lung	lung
31	chr4:10187400-10187800	Enhancers	HUVEC	blood vessel
32	chr4:10187400-10188400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
33	chr4:10187400-10188600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
34	chr4:10187400-10188800	Enhancers	HSMMtube	muscle
35	chr4:10187400-10189200	Enhancers	Left Ventricle	heart
36	chr4:10187400-10191800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
37	chr4:10187600-10187800	Enhancers	Muscle Satellite Cultured Cells	--
38	chr4:10187600-10188200	Enhancers	Osteobl	bone
39	chr4:10187800-10188000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
40	chr4:10187800-10188000	Flanking Active TSS	Fetal Heart	heart
41	chr4:10187800-10189200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
42	chr4:10188000-10188200	Enhancers	Fetal Heart	heart
43	chr4:10188200-10188400	Flanking Active TSS	Fetal Heart	heart
44	chr4:10188200-10190400	Enhancers	K562	blood
45	chr4:10188400-10188600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
46	chr4:10188400-10188800	Enhancers	Fetal Heart	heart
47	chr4:10188600-10190800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
48	chr4:10188800-10194000	Weak transcription	Fetal Heart	heart
49	chr4:10189000-10189200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
50	chr4:10189200-10189400	Enhancers	Right Atrium	heart

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links