Variant report

Variant	nsv432577
Chromosome Location	chr4:10174139-10285348
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1178)
CpG islands
(count:0)
Chromatin interactive
region (count:142)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1178 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

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	chr4:10175936-10176225	K562	blood:	n/a	n/a
3	ARID3A	chr4:10202441-10202778	K562	blood:	n/a	n/a
4	ARID3A	chr4:10188308-10188961	K562	blood:	n/a	n/a
5	ARID3A	chr4:10242016-10242400	K562	blood:	n/a	n/a
6	ARID3A	chr4:10174858-10175646	K562	blood:	n/a	n/a
7	ARID3A	chr4:10241023-10241142	K562	blood:	n/a	n/a
8	ARID3A	chr4:10182036-10184108	K562	blood:	n/a	n/a
9	ARID3A	chr4:10185222-10185607	K562	blood:	n/a	chr4:10185454-10185470
10	ARID3A	chr4:10206944-10207053	HepG2	liver:	n/a	n/a
11	ARID3A	chr4:10206912-10207070	K562	blood:	n/a	n/a
12	ARID3A	chr4:10258670-10258802	K562	blood:	n/a	n/a
13	ATF1	chr4:10184693-10185042	K562	blood:	n/a	n/a
14	ATF1	chr4:10199601-10200004	K562	blood:	n/a	n/a
15	ATF1	chr4:10182216-10183403	K562	blood:	n/a	n/a
16	ATF1	chr4:10241521-10242349	K562	blood:	n/a	n/a
17	ATF1	chr4:10174911-10175439	K562	blood:	n/a	n/a
18	ATF1	chr4:10188186-10188661	K562	blood:	n/a	n/a
19	ATF1	chr4:10187244-10187892	K562	blood:	n/a	n/a
20	ATF3	chr4:10241484-10241931	K562	blood:	n/a	chr4:10241683-10241696
21	ATF3	chr4:10187352-10187768	K562	blood:	n/a	n/a
22	ATF3	chr4:10182376-10183375	K562	blood:	n/a	n/a
23	ATF3	chr4:10174879-10175394	K562	blood:	n/a	n/a
24	BACH1	chr4:10185169-10185293	K562	blood:	n/a	n/a
25	BACH1	chr4:10277398-10277423	K562	blood:	n/a	n/a
26	BACH1	chr4:10174959-10175395	K562	blood:	n/a	n/a
27	BACH1	chr4:10187292-10187596	K562	blood:	n/a	n/a
28	BACH1	chr4:10174334-10174335	K562	blood:	n/a	n/a
29	BACH1	chr4:10236419-10236458	K562	blood:	n/a	n/a
30	BACH1	chr4:10203548-10203807	K562	blood:	n/a	n/a
31	BACH1	chr4:10182278-10183266	K562	blood:	n/a	n/a
32	BACH1	chr4:10258150-10258286	K562	blood:	n/a	n/a
33	BATF	chr4:10182721-10182989	GM12878	blood:	n/a	n/a
34	BCL3	chr4:10182602-10183425	K562	blood:	n/a	chr4:10182894-10182903
35	BCL3	chr4:10206907-10207282	GM12878	blood:	n/a	n/a
36	BCL3	chr4:10191805-10192054	GM12878	blood:	n/a	n/a
37	BCLAF1	chr4:10182260-10183432	K562	blood:	n/a	chr4:10182894-10182903
38	BHLHE40	chr4:10177050-10177337	K562	blood:	n/a	n/a
39	BHLHE40	chr4:10189767-10190685	K562	blood:	n/a	n/a
40	BHLHE40	chr4:10173956-10174337	K562	blood:	n/a	n/a
41	BHLHE40	chr4:10186281-10186687	K562	blood:	n/a	n/a
42	BHLHE40	chr4:10205400-10206307	K562	blood:	n/a	n/a
43	BHLHE40	chr4:10174617-10175572	K562	blood:	n/a	n/a
44	BHLHE40	chr4:10239996-10240058	K562	blood:	n/a	n/a
45	BHLHE40	chr4:10187295-10189374	K562	blood:	n/a	n/a
46	BHLHE40	chr4:10181734-10182063	K562	blood:	n/a	n/a
47	BHLHE40	chr4:10184623-10185411	K562	blood:	n/a	n/a
48	BHLHE40	chr4:10199645-10199963	K562	blood:	n/a	n/a
49	BHLHE40	chr4:10215328-10215399	K562	blood:	n/a	n/a
50	BHLHE40	chr4:10202450-10202808	K562	blood:	n/a	n/a

No data

(count:142 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr4:10181426..10184302-chr4:10237283..10239761,3	K562	blood:
2	chr4:10250648..10253943-chr4:10254760..10258340,4	K562	blood:
3	chr4:10109894..10126876-chr4:10164648..10190106,79	K562	blood:
4	chr4:10116403..10118365-chr4:10196419..10198714,2	K562	blood:
5	chr4:10181426..10184302-chr4:10237283..10239761,3	K562	blood:
6	chr4:10181069..10182933-chr4:10345413..10347984,3	K562	blood:
7	chr4:10117842..10119536-chr4:10257217..10259311,2	K562	blood:
8	chr4:10173721..10176602-chr4:10326116..10328946,2	K562	blood:
9	chr4:10211963..10215052-chr4:10219787..10222880,4	K562	blood:
10	chr4:10117656..10120785-chr4:10200069..10203011,5	K562	blood:
11	chr4:10274788..10276860-chr4:10285063..10286717,2	K562	blood:
12	chr4:10181386..10184366-chr4:10364568..10366943,2	K562	blood:
13	chr4:10262775..10265010-chr4:10265780..10268025,2	K562	blood:
14	chr4:10184632..10187184-chr4:10400763..10402949,2	K562	blood:
15	chr4:10171114..10171975-chr4:10185300..10186046,2	K562	blood:
16	chr4:10249783..10252189-chr4:10254326..10257178,3	K562	blood:
17	chr4:10194015..10194637-chr4:10405680..10406337,2	MCF-7	breast:
18	chr4:10266281..10269337-chr4:10269908..10272870,3	K562	blood:
19	chr4:10266886..10269236-chr4:10273082..10275523,2	K562	blood:
20	chr4:10210284..10212005-chr4:10213695..10216562,2	K562	blood:
21	chr4:10175247..10177327-chr4:10228151..10230198,2	K562	blood:
22	chr4:10182494..10184635-chr4:10284696..10287291,2	K562	blood:
23	chr4:10210505..10213622-chr4:10215055..10217234,4	K562	blood:
24	chr4:10266886..10269236-chr4:10273082..10275523,2	K562	blood:
25	chr4:10207125..10208799-chr4:10284967..10286577,2	K562	blood:
26	chr4:10249783..10252189-chr4:10254326..10257178,3	K562	blood:
27	chr4:10182154..10184410-chr4:10456824..10459646,5	K562	blood:
28	chr4:10182494..10184107-chr4:10284696..10287149,2	K562	blood:
29	chr4:10254662..10256804-chr4:10260995..10262728,2	K562	blood:
30	chr4:10124578..10127302-chr4:10186119..10188725,2	K562	blood:
31	chr4:10204306..10206166-chr4:10241229..10242983,2	K562	blood:
32	chr4:10206033..10207589-chr4:10220077..10222198,2	K562	blood:
33	chr4:10114665..10116599-chr4:10227448..10229354,2	K562	blood:
34	chr4:10234367..10236533-chr4:10242137..10244033,2	K562	blood:
35	chr4:10182716..10185413-chr4:10249318..10252021,2	K562	blood:
36	chr4:10175466..10178390-chr4:10458313..10460581,2	K562	blood:
37	chr4:10204306..10206166-chr4:10241229..10242983,2	K562	blood:
38	chr4:10182716..10185413-chr4:10249318..10252021,2	K562	blood:
39	chr4:10210284..10212005-chr4:10213695..10216562,2	K562	blood:
40	chr4:10262775..10265010-chr4:10265780..10268025,2	K562	blood:
41	chr4:10181799..10184639-chr4:10262185..10264664,2	K562	blood:
42	chr4:10156172..10158401-chr4:10178392..10179954,2	K562	blood:
43	chr4:10171115..10173658-chr4:10254307..10257090,2	K562	blood:
44	chr4:10121764..10123838-chr4:10222085..10224894,2	K562	blood:
45	chr4:10194345..10195861-chr4:10210275..10213111,2	K562	blood:
46	chr4:10271663..10274322-chr4:10278537..10280895,2	K562	blood:
47	chr4:10114162..10115900-chr4:10186432..10189186,2	K562	blood:
48	chr4:10242448..10244811-chr4:10340269..10342798,2	K562	blood:
49	chr4:10180113..10182537-chr4:10415151..10418343,3	K562	blood:
50	chr4:10181292..10183606-chr4:10239969..10241672,2	K562	blood:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-WDR1-10	chr4:10261069-10261762	NONHSAT095491
2	lnc-WDR1-11	chr4:10269519-10269855	NONHSAT095492
3	lnc-WDR1-9	chr4:10256550-10258245	NONHSAT095490
4	lnc-WDR1-7	chr4:10201447-10202296	NONHSAT095488

No data

Variant related genes	Relation type
ENSG00000248777	TF binding region
ENSG00000271544	TF binding region
ENSG00000250040	TF binding region
ENSG00000251296	TF binding region
ENSG00000250074	TF binding region
ENSG00000250573	TF binding region
ENSG00000250040	chromatin interactions
ENSG00000248777	chromatin interactions
ENSG00000109787	chromatin interactions
ENSG00000178163	chromatin interactions
ENSG00000223086	chromatin interactions
ENSG00000250573	chromatin interactions
ENSG00000231160	chromatin interactions
ENSG00000196355	chromatin interactions
ENSG00000071127	chromatin interactions
ENSG00000271544	chromatin interactions

Extended variants
information (count: 7038 )
Associated
traits (count: 57 )

Variant overlapped rSNPs/rCNVs (count:7038 , 50 per page) page: 1 2 3 4 5 6 7 ... 141

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	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
2	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
3	rs577039175	chr4:10174180-10174181	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs534830087	chr4:10174189-10174190	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	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
6	rs558672936	chr4:10174203-10174204	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs188401313	chr4:10174211-10174212	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs4697721	chr4:10174217-10174218	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
9	rs560313435	chr4:10174233-10174234	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs576341903	chr4:10174237-10174238	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs532867763	chr4:10174239-10174240	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs35185744	chr4:10174262-10174263	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs397723653	chr4:10174272-10174273	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs565458838	chr4:10174310-10174311	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs532631768	chr4:10174350-10174351	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs180819233	chr4:10174363-10174364	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs368624956	chr4:10174364-10174365	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs372313809	chr4:10174384-10174385	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs56838074	chr4:10174403-10174404	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs201074316	chr4:10174405-10174406	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs202205545	chr4:10174406-10174407	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs529785653	chr4:10174412-10174413	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs186581537	chr4:10174441-10174442	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs569663578	chr4:10174445-10174446	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs571732442	chr4:10174460-10174461	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs374249801	chr4:10174516-10174517	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs552117146	chr4:10174522-10174523	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs4697954	chr4:10174529-10174530	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
29	rs75987279	chr4:10174544-10174545	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs200963702	chr4:10174574-10174575	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs386671612	chr4:10174575-10174576	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs202153104	chr4:10174584-10174585	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs190841282	chr4:10174588-10174589	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs568249487	chr4:10174606-10174607	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs548281274	chr4:10174608-10174609	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs112941531	chr4:10174613-10174614	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs554556050	chr4:10174665-10174666	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs143831311	chr4:10174692-10174693	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs76294065	chr4:10174718-10174719	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs181966982	chr4:10174738-10174739	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs569487013	chr4:10174761-10174762	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs146874150	chr4:10174778-10174779	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs6449338	chr4:10174781-10174782	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
44	rs558870152	chr4:10174787-10174788	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs552383363	chr4:10174816-10174817	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs570636299	chr4:10174823-10174824	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs186592789	chr4:10174830-10174831	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs115454882	chr4:10174839-10174840	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs140727462	chr4:10174844-10174845	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs375280046	chr4:10174849-10174850	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:57)

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
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:579 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:10166000-10175400	Weak transcription	Pancreas	Pancrea
2	chr4:10167200-10174400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
3	chr4:10170200-10174200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
4	chr4:10171400-10175600	Enhancers	Fetal Heart	heart
5	chr4:10171600-10176400	Flanking Active TSS	K562	blood
6	chr4:10172400-10174200	Weak transcription	Colon Smooth Muscle	Colon
7	chr4:10172400-10174800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
8	chr4:10172400-10175400	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
9	chr4:10172400-10176400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
10	chr4:10172400-10176600	Enhancers	HMEC	breast
11	chr4:10172600-10174800	Enhancers	Fetal Intestine Small	intestine
12	chr4:10172600-10176400	Enhancers	Duodenum Mucosa	Duodenum
13	chr4:10172600-10176400	Enhancers	NHEK	skin
14	chr4:10172800-10178400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
15	chr4:10173200-10174400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
16	chr4:10173400-10174400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
17	chr4:10173400-10175600	Weak transcription	Rectal Mucosa Donor 29	rectum
18	chr4:10173400-10176400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
19	chr4:10173600-10174200	Enhancers	H1 Cell Line	embryonic stem cell
20	chr4:10173600-10175800	Enhancers	Cortex derived primary cultured neurospheres	brain
21	chr4:10173600-10175800	Enhancers	HUVEC	blood vessel
22	chr4:10173600-10176400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
23	chr4:10173600-10178000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
24	chr4:10173800-10174200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
25	chr4:10173800-10174200	Enhancers	Colonic Mucosa	Colon
26	chr4:10173800-10174400	Enhancers	Fetal Muscle Trunk	muscle
27	chr4:10173800-10174400	Enhancers	Psoas Muscle	Psoas
28	chr4:10173800-10174600	Enhancers	iPS-18 Cell Line	embryonic stem cell
29	chr4:10173800-10174800	Enhancers	Sigmoid Colon	Sigmoid Colon
30	chr4:10173800-10175000	Weak transcription	Stomach Mucosa	stomach
31	chr4:10173800-10176000	Enhancers	Fetal Lung	lung
32	chr4:10173800-10176600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
33	chr4:10173800-10177200	Enhancers	Fetal Muscle Leg	muscle
34	chr4:10173800-10178000	Enhancers	Placenta	Placenta
35	chr4:10174000-10174200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
36	chr4:10174000-10174200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
37	chr4:10174000-10174200	Enhancers	Aorta	Aorta
38	chr4:10174000-10174400	Flanking Active TSS	Breast Myoepithelial Primary Cells	Breast
39	chr4:10174000-10174400	Weak transcription	Rectal Mucosa Donor 31	rectum
40	chr4:10174000-10174800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
41	chr4:10174000-10175200	Enhancers	Skeletal Muscle Male	skeletal muscle
42	chr4:10174000-10176000	Enhancers	Muscle Satellite Cultured Cells	--
43	chr4:10174000-10176200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
44	chr4:10174000-10176200	Enhancers	Right Atrium	heart
45	chr4:10174000-10176400	Enhancers	Lung	lung
46	chr4:10174000-10177000	Enhancers	Rectal Smooth Muscle	rectum
47	chr4:10174000-10177200	Enhancers	Gastric	stomach
48	chr4:10174000-10177200	Enhancers	Skeletal Muscle Female	skeletal muscle
49	chr4:10174000-10177400	Enhancers	Fetal Thymus	thymus
50	chr4:10174000-10177600	Enhancers	Adipose Nuclei	Adipose

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