Variant report

Variant	nsv1009794
Chromosome Location	chr4:10173696-10184002
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:384)
CpG islands
(count:0)
Chromatin interactive
region (count:44)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:384 , 50 per page) page: 1 2 3 4 5 6 7 8

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	chr4:10174858-10175646	K562	blood:	n/a	n/a
3	ARID3A	chr4:10175936-10176225	K562	blood:	n/a	n/a
4	ATF1	chr4:10182216-10183403	K562	blood:	n/a	n/a
5	ATF1	chr4:10174911-10175439	K562	blood:	n/a	n/a
6	ATF3	chr4:10182376-10183375	K562	blood:	n/a	n/a
7	ATF3	chr4:10174879-10175394	K562	blood:	n/a	n/a
8	BACH1	chr4:10174334-10174335	K562	blood:	n/a	n/a
9	BACH1	chr4:10174959-10175395	K562	blood:	n/a	n/a
10	BACH1	chr4:10182278-10183266	K562	blood:	n/a	n/a
11	BATF	chr4:10182721-10182989	GM12878	blood:	n/a	n/a
12	BCL3	chr4:10182602-10183425	K562	blood:	n/a	chr4:10182894-10182903
13	BCLAF1	chr4:10182260-10183432	K562	blood:	n/a	chr4:10182894-10182903
14	BHLHE40	chr4:10173956-10174337	K562	blood:	n/a	n/a
15	BHLHE40	chr4:10182270-10183899	K562	blood:	n/a	n/a
16	BHLHE40	chr4:10174617-10175572	K562	blood:	n/a	n/a
17	BHLHE40	chr4:10175935-10175937	K562	blood:	n/a	n/a
18	BHLHE40	chr4:10181734-10182063	K562	blood:	n/a	n/a
19	BHLHE40	chr4:10177050-10177337	K562	blood:	n/a	n/a
20	CBX3	chr4:10182158-10184114	K562	blood:	n/a	n/a
21	CBX3	chr4:10174481-10175493	K562	blood:	n/a	n/a
22	CBX3	chr4:10182206-10184538	K562	blood:	n/a	n/a
23	CCNT2	chr4:10174708-10175366	K562	blood:	n/a	n/a
24	CCNT2	chr4:10173523-10174275	K562	blood:	n/a	n/a
25	CCNT2	chr4:10182296-10183917	K562	blood:	n/a	n/a
26	CCNT2	chr4:10181104-10181327	K562	blood:	n/a	n/a
27	CCNT2	chr4:10176073-10176380	K562	blood:	n/a	n/a
28	CEBPB	chr4:10175016-10175532	K562	blood:	n/a	n/a
29	CEBPB	chr4:10174841-10175497	K562	blood:	n/a	n/a
30	CEBPB	chr4:10183343-10183757	IMR90	lung:	n/a	n/a
31	CEBPB	chr4:10182244-10183976	K562	blood:	n/a	n/a
32	CEBPB	chr4:10182703-10183002	K562	blood:	n/a	n/a
33	CEBPB	chr4:10181400-10181729	K562	blood:	n/a	chr4:10181570-10181583
34	CEBPB	chr4:10182153-10184069	K562	blood:	n/a	n/a
35	CEBPD	chr4:10174956-10175446	K562	blood:	n/a	n/a
36	CEBPD	chr4:10182224-10183672	K562	blood:	n/a	n/a
37	CEBPD	chr4:10182152-10183632	K562	blood:	n/a	n/a
38	CHD2	chr4:10180631-10180669	K562	blood:	n/a	n/a
39	CHD2	chr4:10174744-10175406	K562	blood:	n/a	n/a
40	CHD2	chr4:10182381-10183874	K562	blood:	n/a	n/a
41	CREB1	chr4:10182146-10183616	K562	blood:	n/a	n/a
42	CREB1	chr4:10182330-10183370	K562	blood:	n/a	n/a
43	CTCF	chr4:10175040-10175190	HUVEC	blood vessel:	n/a	n/a
44	CTCF	chr4:10175025-10175216	NHEK	skin:	n/a	n/a
45	CTCF	chr4:10175040-10175190	HCT-116	colon:	n/a	n/a
46	CTCF	chr4:10175009-10175215	MCF-7	breast:	n/a	n/a
47	CTCF	chr4:10175060-10175210	AG10803	skin:	n/a	n/a
48	CTCF	chr4:10175020-10175170	RPTEC	kidney:	n/a	n/a
49	CTCF	chr4:10175020-10175170	AoAF	blood vessel:	n/a	n/a
50	CTCF	chr4:10175060-10175210	HMEC	breast:	n/a	n/a

No data

(count:44 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:10180113..10182537-chr4:10415151..10418343,3	K562	blood:
2	chr4:10181898..10186356-chr4:10317430..10320755,4	K562	blood:
3	chr4:10112946..10115430-chr4:10181535..10185097,4	K562	blood:
4	chr4:10182491..10184302-chr4:10237283..10239761,2	K562	blood:
5	chr4:10181292..10183606-chr4:10239969..10241672,2	K562	blood:
6	chr4:10159584..10164126-chr4:10173679..10176923,6	K562	blood:
7	chr4:10181802..10184742-chr4:10401642..10403855,2	K562	blood:
8	chr4:10175466..10178390-chr4:10458313..10460581,2	K562	blood:
9	chr4:10137227..10139603-chr4:10183343..10185587,3	K562	blood:
10	chr4:10182452..10185153-chr4:10405566..10407454,2	K562	blood:
11	chr4:10182435..10184114-chr4:10441654..10444481,2	K562	blood:
12	chr4:10156172..10158401-chr4:10178392..10179954,2	K562	blood:
13	chr4:10182073..10186416-chr4:10457121..10461088,7	K562	blood:
14	chr4:10109894..10126876-chr4:10164648..10190106,79	K562	blood:
15	chr4:10182154..10184410-chr4:10456824..10459646,5	K562	blood:
16	chr4:10173514..10177541-chr4:10443857..10446930,3	K562	blood:
17	chr4:10183994..10188822-chr4:10326557..10329780,4	K562	blood:
18	chr4:10173856..10175564-chr8:118809117..118811670,2	MCF-7	breast:
19	chr4:10179301..10181367-chr4:10408418..10410454,2	K562	blood:
20	chr4:10180991..10184001-chr4:10327240..10329402,3	K562	blood:
21	chr4:10180539..10184306-chr4:10401076..10403855,3	K562	blood:
22	chr4:10116325..10123199-chr4:10169149..10177855,21	K562	blood:
23	chr4:10160663..10163901-chr4:10177399..10182680,5	K562	blood:
24	chr4:10181426..10184302-chr4:10237283..10239761,3	K562	blood:
25	chr4:10177971..10181867-chr4:10459708..10464611,4	K562	blood:
26	chr4:10182494..10184635-chr4:10284696..10287291,2	K562	blood:
27	chr4:10116716..10122622-chr4:10178049..10187480,27	K562	blood:
28	chr4:10181069..10182933-chr4:10345413..10347984,3	K562	blood:
29	chr4:10181502..10184182-chr4:38665329..38667544,2	K562	blood:
30	chr4:10175247..10177327-chr4:10228151..10230198,2	K562	blood:
31	chr4:10171484..10174076-chr4:10483105..10485442,2	K562	blood:
32	chr4:10181799..10184639-chr4:10262185..10264664,2	K562	blood:
33	chr4:10179915..10182843-chr4:10450700..10452839,2	K562	blood:
34	chr4:10180991..10182787-chr4:10327240..10329402,2	K562	blood:
35	chr4:10182716..10185413-chr4:10249318..10252021,2	K562	blood:
36	chr4:10181386..10184366-chr4:10364568..10366943,2	K562	blood:
37	chr4:10173721..10176602-chr4:10326116..10328946,2	K562	blood:
38	chr4:10182494..10184107-chr4:10284696..10287149,2	K562	blood:
39	chr4:10182377..10185038-chr4:10453503..10456156,2	K562	blood:
40	chr4:10174527..10176209-chr4:10240126..10241692,2	K562	blood:
41	chr4:10132922..10135214-chr4:10181103..10182859,2	K562	blood:
42	chr4:10182377..10184143-chr4:10453503..10455042,2	K562	blood:
43	chr4:10179643..10181436-chr4:10389855..10391388,2	K562	blood:
44	chr4:10172802..10175283-chr4:10404131..10407127,2	K562	blood:

No data

Variant related genes	Relation type
ENSG00000251296	TF binding region
ENSG00000196355	chromatin interactions
ENSG00000223086	chromatin interactions
ENSG00000071127	chromatin interactions
ENSG00000109787	chromatin interactions
ENSG00000178163	chromatin interactions
ENSG00000231160	chromatin interactions

Extended variants
information (count: 797 )
Associated
traits (count: 54 )

Variant overlapped rSNPs/rCNVs (count:797 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10034405	chr4:10173696-10173697	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs547971324	chr4:10173697-10173698	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs148105257	chr4:10173707-10173708	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs571695925	chr4:10173716-10173717	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs542545064	chr4:10173731-10173732	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs184578027	chr4:10173741-10173742	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs112669048	chr4:10173743-10173744	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs4697953	chr4:10173753-10173754	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs564889859	chr4:10173767-10173768	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs533515831	chr4:10173778-10173779	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs545511213	chr4:10173789-10173790	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs150550975	chr4:10173790-10173791	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs114748506	chr4:10173798-10173799	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs138582429	chr4:10173808-10173809	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs375761057	chr4:10173811-10173812	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs531871423	chr4:10173819-10173820	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs142837402	chr4:10173829-10173830	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs147425151	chr4:10173832-10173833	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs376298469	chr4:10173846-10173847	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs139801749	chr4:10173865-10173866	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs373790071	chr4:10173885-10173886	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs55760253	chr4:10173889-10173890	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
23	rs535865844	chr4:10173923-10173924	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs549916177	chr4:10173936-10173937	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs570393490	chr4:10173937-10173938	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs112228019	chr4:10173947-10173948	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs76903922	chr4:10173951-10173952	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs115188329	chr4:10173954-10173955	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs114231310	chr4:10173964-10173965	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs143883619	chr4:10173975-10173976	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs560590566	chr4:10173992-10173993	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs114656953	chr4:10173995-10173996	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs77093467	chr4:10173996-10173997	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs148625865	chr4:10174013-10174014	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs142119452	chr4:10174022-10174023	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs79714536	chr4:10174035-10174036	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs550196225	chr4:10174060-10174061	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs541988993	chr4:10174078-10174079	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs151180417	chr4:10174091-10174092	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs532543326	chr4:10174092-10174093	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs547556119	chr4:10174101-10174102	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs565453132	chr4:10174113-10174114	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs112967961	chr4:10174114-10174115	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs548169768	chr4:10174117-10174118	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs569542092	chr4:10174135-10174136	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs4697718	chr4:10174139-10174140	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
47	rs4697719	chr4:10174158-10174159	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
48	rs577039175	chr4:10174180-10174181	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs534830087	chr4:10174189-10174190	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs4697720	chr4:10174190-10174191	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance

Variant related diseases (count:54)

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

Chromatin state (count:270 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:10165000-10174000	Weak transcription	Gastric	stomach
2	chr4:10165200-10173800	Weak transcription	Rectal Mucosa Donor 31	rectum
3	chr4:10166000-10175400	Weak transcription	Pancreas	Pancrea
4	chr4:10166200-10174000	Weak transcription	Left Ventricle	heart
5	chr4:10167200-10174400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
6	chr4:10170200-10174000	Weak transcription	Fetal Thymus	thymus
7	chr4:10170200-10174000	Weak transcription	Right Atrium	heart
8	chr4:10170200-10174200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
9	chr4:10170400-10173800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
10	chr4:10170400-10174000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
11	chr4:10171000-10174000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
12	chr4:10171400-10175600	Enhancers	Fetal Heart	heart
13	chr4:10171600-10176400	Flanking Active TSS	K562	blood
14	chr4:10172400-10174200	Weak transcription	Colon Smooth Muscle	Colon
15	chr4:10172400-10174800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
16	chr4:10172400-10175400	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
17	chr4:10172400-10176400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
18	chr4:10172400-10176600	Enhancers	HMEC	breast
19	chr4:10172600-10173800	Enhancers	Stomach Mucosa	stomach
20	chr4:10172600-10174800	Enhancers	Fetal Intestine Small	intestine
21	chr4:10172600-10176400	Enhancers	Duodenum Mucosa	Duodenum
22	chr4:10172600-10176400	Enhancers	NHEK	skin
23	chr4:10172800-10173800	Weak transcription	Placenta	Placenta
24	chr4:10172800-10173800	Weak transcription	Sigmoid Colon	Sigmoid Colon
25	chr4:10172800-10174000	Weak transcription	HSMM	muscle
26	chr4:10172800-10178400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
27	chr4:10173000-10174000	Weak transcription	Adipose Nuclei	Adipose
28	chr4:10173200-10174400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
29	chr4:10173400-10174400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
30	chr4:10173400-10175600	Weak transcription	Rectal Mucosa Donor 29	rectum
31	chr4:10173400-10176400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
32	chr4:10173600-10174000	Enhancers	Breast Myoepithelial Primary Cells	Breast
33	chr4:10173600-10174200	Enhancers	H1 Cell Line	embryonic stem cell
34	chr4:10173600-10175800	Enhancers	Cortex derived primary cultured neurospheres	brain
35	chr4:10173600-10175800	Enhancers	HUVEC	blood vessel
36	chr4:10173600-10176400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
37	chr4:10173600-10178000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
38	chr4:10173800-10174000	Enhancers	Rectal Mucosa Donor 31	rectum
39	chr4:10173800-10174200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
40	chr4:10173800-10174200	Enhancers	Colonic Mucosa	Colon
41	chr4:10173800-10174400	Enhancers	Fetal Muscle Trunk	muscle
42	chr4:10173800-10174400	Enhancers	Psoas Muscle	Psoas
43	chr4:10173800-10174600	Enhancers	iPS-18 Cell Line	embryonic stem cell
44	chr4:10173800-10174800	Enhancers	Sigmoid Colon	Sigmoid Colon
45	chr4:10173800-10175000	Weak transcription	Stomach Mucosa	stomach
46	chr4:10173800-10176000	Enhancers	Fetal Lung	lung
47	chr4:10173800-10176600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
48	chr4:10173800-10177200	Enhancers	Fetal Muscle Leg	muscle
49	chr4:10173800-10178000	Enhancers	Placenta	Placenta
50	chr4:10174000-10174200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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