Variant report

Variant	nsv1010383
Chromosome Location	chr4:10169535-10244955
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1075)
CpG islands
(count:0)
Chromatin interactive
region (count:115)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1075 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:10206912-10207070	K562	blood:	n/a	n/a
2	ARID3A	chr4:10182036-10184108	K562	blood:	n/a	n/a
3	ARID3A	chr4:10206944-10207053	HepG2	liver:	n/a	n/a
4	ARID3A	chr4:10242016-10242400	K562	blood:	n/a	n/a
5	ARID3A	chr4:10202441-10202778	K562	blood:	n/a	n/a
6	ARID3A	chr4:10185222-10185607	K562	blood:	n/a	chr4:10185454-10185470
7	ARID3A	chr4:10175936-10176225	K562	blood:	n/a	n/a
8	ARID3A	chr4:10186847-10188023	K562	blood:	n/a	n/a
9	ARID3A	chr4:10241023-10241142	K562	blood:	n/a	n/a
10	ARID3A	chr4:10174858-10175646	K562	blood:	n/a	n/a
11	ARID3A	chr4:10171356-10172376	K562	blood:	n/a	n/a
12	ARID3A	chr4:10172580-10173201	K562	blood:	n/a	n/a
13	ARID3A	chr4:10188308-10188961	K562	blood:	n/a	n/a
14	ATF1	chr4:10172681-10173016	K562	blood:	n/a	n/a
15	ATF1	chr4:10184693-10185042	K562	blood:	n/a	n/a
16	ATF1	chr4:10241521-10242349	K562	blood:	n/a	n/a
17	ATF1	chr4:10182216-10183403	K562	blood:	n/a	n/a
18	ATF1	chr4:10188186-10188661	K562	blood:	n/a	n/a
19	ATF1	chr4:10199601-10200004	K562	blood:	n/a	n/a
20	ATF1	chr4:10174911-10175439	K562	blood:	n/a	n/a
21	ATF1	chr4:10187244-10187892	K562	blood:	n/a	n/a
22	ATF1	chr4:10171263-10171804	K562	blood:	n/a	n/a
23	ATF3	chr4:10187352-10187768	K562	blood:	n/a	n/a
24	ATF3	chr4:10182376-10183375	K562	blood:	n/a	n/a
25	ATF3	chr4:10241484-10241931	K562	blood:	n/a	chr4:10241683-10241696
26	ATF3	chr4:10174879-10175394	K562	blood:	n/a	n/a
27	BACH1	chr4:10174334-10174335	K562	blood:	n/a	n/a
28	BACH1	chr4:10182278-10183266	K562	blood:	n/a	n/a
29	BACH1	chr4:10185169-10185293	K562	blood:	n/a	n/a
30	BACH1	chr4:10203548-10203807	K562	blood:	n/a	n/a
31	BACH1	chr4:10174959-10175395	K562	blood:	n/a	n/a
32	BACH1	chr4:10236419-10236458	K562	blood:	n/a	n/a
33	BACH1	chr4:10187292-10187596	K562	blood:	n/a	n/a
34	BATF	chr4:10182721-10182989	GM12878	blood:	n/a	n/a
35	BCL3	chr4:10182602-10183425	K562	blood:	n/a	chr4:10182894-10182903
36	BCL3	chr4:10191805-10192054	GM12878	blood:	n/a	n/a
37	BCL3	chr4:10206907-10207282	GM12878	blood:	n/a	n/a
38	BCLAF1	chr4:10182260-10183432	K562	blood:	n/a	chr4:10182894-10182903
39	BHLHE40	chr4:10215328-10215399	K562	blood:	n/a	n/a
40	BHLHE40	chr4:10182270-10183899	K562	blood:	n/a	n/a
41	BHLHE40	chr4:10187295-10189374	K562	blood:	n/a	n/a
42	BHLHE40	chr4:10205400-10206307	K562	blood:	n/a	n/a
43	BHLHE40	chr4:10202450-10202808	K562	blood:	n/a	n/a
44	BHLHE40	chr4:10173956-10174337	K562	blood:	n/a	n/a
45	BHLHE40	chr4:10241629-10242291	K562	blood:	n/a	n/a
46	BHLHE40	chr4:10181734-10182063	K562	blood:	n/a	n/a
47	BHLHE40	chr4:10193880-10194273	K562	blood:	n/a	n/a
48	BHLHE40	chr4:10207080-10207159	K562	blood:	n/a	n/a
49	BHLHE40	chr4:10174617-10175572	K562	blood:	n/a	n/a
50	BHLHE40	chr4:10189767-10190685	K562	blood:	n/a	n/a

No data

(count:115 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr4:10177971..10181867-chr4:10459708..10464611,4	K562	blood:
2	chr4:10132922..10135214-chr4:10181103..10182859,2	K562	blood:
3	chr4:10182073..10186416-chr4:10457121..10461088,7	K562	blood:
4	chr4:10181802..10184742-chr4:10401642..10403855,2	K562	blood:
5	chr4:10186571..10188279-chr4:10316070..10319056,2	K562	blood:
6	chr4:10204306..10206166-chr4:10241229..10242983,2	K562	blood:
7	chr4:10118276..10120462-chr4:10220218..10222885,3	K562	blood:
8	chr4:10211963..10215052-chr4:10219787..10222880,4	K562	blood:
9	chr4:10234367..10236533-chr4:10242137..10244033,2	K562	blood:
10	chr4:10182435..10184114-chr4:10441654..10444481,2	K562	blood:
11	chr4:10182452..10185153-chr4:10405566..10407454,2	K562	blood:
12	chr4:10182154..10184410-chr4:10456824..10459646,5	K562	blood:
13	chr4:10226621..10229156-chr4:10309809..10312332,2	K562	blood:
14	chr4:10202106..10207051-chr4:10207371..10210794,7	K562	blood:
15	chr4:10187220..10189194-chr4:10403510..10406450,3	K562	blood:
16	chr4:10173856..10175564-chr8:118809117..118811670,2	MCF-7	breast:
17	chr4:10242448..10244811-chr4:10340269..10342798,2	K562	blood:
18	chr4:10182494..10184635-chr4:10284696..10287291,2	K562	blood:
19	chr4:10119416..10121988-chr4:10218168..10219976,2	K562	blood:
20	chr4:10182491..10184302-chr4:10237283..10239761,2	K562	blood:
21	chr4:10124578..10127302-chr4:10186119..10188725,2	K562	blood:
22	chr4:10180991..10184001-chr4:10327240..10329402,3	K562	blood:
23	chr4:10179301..10181367-chr4:10408418..10410454,2	K562	blood:
24	chr4:10203874..10205718-chr4:10217408..10219978,2	K562	blood:
25	chr4:10182377..10184143-chr4:10453503..10455042,2	K562	blood:
26	chr4:10175247..10177327-chr4:10228151..10230198,2	K562	blood:
27	chr4:10137227..10139603-chr4:10183343..10185587,3	K562	blood:
28	chr4:10210505..10213622-chr4:10215055..10217234,4	K562	blood:
29	chr4:10180113..10182537-chr4:10415151..10418343,3	K562	blood:
30	chr4:10171114..10171975-chr4:10185300..10186046,2	K562	blood:
31	chr4:10117378..10119328-chr4:10192047..10193702,2	K562	blood:
32	chr4:10109894..10126876-chr4:10164648..10190106,79	K562	blood:
33	chr4:10206033..10207589-chr4:10220077..10222198,2	K562	blood:
34	chr4:10117656..10120785-chr4:10200069..10203011,5	K562	blood:
35	chr4:10119371..10120949-chr4:10187732..10190413,2	K562	blood:
36	chr4:10234367..10237486-chr4:10239791..10244033,5	K562	blood:
37	chr4:10206033..10207589-chr4:10220077..10222198,2	K562	blood:
38	chr4:10194345..10195861-chr4:10210275..10213111,2	K562	blood:
39	chr4:10119817..10121406-chr4:10243789..10245878,2	K562	blood:
40	chr4:10180539..10184306-chr4:10401076..10403855,3	K562	blood:
41	chr4:10181426..10184302-chr4:10237283..10239761,3	K562	blood:
42	chr4:10181898..10186356-chr4:10317430..10320755,4	K562	blood:
43	chr4:10171115..10173658-chr4:10254307..10257090,2	K562	blood:
44	chr4:10236259..10238046-chr4:10240029..10241603,2	K562	blood:
45	chr4:10203874..10205718-chr4:10217408..10219978,2	K562	blood:
46	chr4:10155458..10156959-chr4:10169942..10172746,2	K562	blood:
47	chr4:10218238..10220165-chr4:10231013..10232714,2	K562	blood:
48	chr4:10231830..10233378-chr4:10235064..10237402,2	K562	blood:
49	chr4:10244335..10247662-chr4:10255817..10258798,3	K562	blood:
50	chr4:10174527..10176209-chr4:10240126..10241692,2	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
ENSG00000251296	TF binding region
ENSG00000109787	chromatin interactions
ENSG00000250040	chromatin interactions
ENSG00000196355	chromatin interactions
ENSG00000248777	chromatin interactions
ENSG00000071127	chromatin interactions
ENSG00000223086	chromatin interactions
ENSG00000231160	chromatin interactions
ENSG00000271544	chromatin interactions
ENSG00000178163	chromatin interactions

Extended variants
information (count: 4605 )
Associated
traits (count: 56 )

Variant overlapped rSNPs/rCNVs (count:4605 , 50 per page) page: 1 2 3 4 5 6 7 ... 93

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1990471	chr4:10169535-10169536	Enhancers Weak transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
2	rs62288888	chr4:10169545-10169546	Enhancers Weak transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs12506543	chr4:10169547-10169548	Enhancers Weak transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs181091334	chr4:10169551-10169552	Enhancers Weak transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs140370426	chr4:10169597-10169598	Enhancers Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs533313856	chr4:10169603-10169604	Enhancers Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs34216420	chr4:10169642-10169643	Enhancers Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs186259968	chr4:10169729-10169730	Enhancers Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs145136916	chr4:10169735-10169736	Enhancers Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs111737370	chr4:10169738-10169739	Enhancers Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs4697946	chr4:10169744-10169745	Enhancers Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
12	rs535516856	chr4:10169748-10169749	Enhancers Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs556938060	chr4:10169761-10169762	Enhancers Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs575229259	chr4:10169767-10169768	Enhancers Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs73218783	chr4:10169771-10169772	Enhancers Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs112150188	chr4:10169772-10169773	Enhancers Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs79238763	chr4:10169775-10169776	Enhancers Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs149890822	chr4:10169776-10169777	Enhancers Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs75331428	chr4:10169777-10169778	Enhancers Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs573410063	chr4:10169779-10169780	Enhancers Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs547727212	chr4:10169803-10169804	Enhancers Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs78868507	chr4:10169823-10169824	Enhancers Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs575109750	chr4:10169883-10169884	Enhancers Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs147308858	chr4:10169887-10169888	Enhancers Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs562228051	chr4:10169889-10169890	Enhancers Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs529005886	chr4:10169894-10169895	Enhancers Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs544323282	chr4:10169900-10169901	Enhancers Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs562510243	chr4:10169901-10169902	Enhancers Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs532944078	chr4:10169902-10169903	Enhancers Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs551684375	chr4:10169918-10169919	Enhancers Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs6850146	chr4:10169936-10169937	Enhancers Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
32	rs372387449	chr4:10169974-10169975	Enhancers Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs182540864	chr4:10169976-10169977	Enhancers Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs143044167	chr4:10169977-10169978	Enhancers Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs187667357	chr4:10169978-10169979	Enhancers Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs372885120	chr4:10169982-10169983	Enhancers Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs535599403	chr4:10170002-10170003	Enhancers Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs75562179	chr4:10170005-10170006	Enhancers Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs11940795	chr4:10170019-10170020	Enhancers Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs573120640	chr4:10170038-10170039	Enhancers Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs7692419	chr4:10170045-10170046	Enhancers Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
42	rs191799134	chr4:10170063-10170064	Enhancers Weak transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs573471886	chr4:10170084-10170085	Enhancers Weak transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs370160384	chr4:10170094-10170095	Enhancers Weak transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs7679297	chr4:10170105-10170106	Enhancers Weak transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
46	rs183075766	chr4:10170117-10170118	Enhancers Weak transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs113922469	chr4:10170118-10170119	Enhancers Weak transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs187407921	chr4:10170123-10170124	Enhancers Weak transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs190340439	chr4:10170137-10170138	Enhancers Weak transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs182784478	chr4:10170138-10170139	Enhancers Weak transcription Genic enhancers	TF binding region 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:501 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:10159800-10172600	Weak transcription	NHEK	skin
2	chr4:10164200-10169600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
3	chr4:10164800-10169600	Weak transcription	Sigmoid Colon	Sigmoid Colon
4	chr4:10165000-10174000	Weak transcription	Gastric	stomach
5	chr4:10165200-10173800	Weak transcription	Rectal Mucosa Donor 31	rectum
6	chr4:10165400-10172600	Weak transcription	Stomach Mucosa	stomach
7	chr4:10165600-10169800	Weak transcription	Fetal Intestine Small	intestine
8	chr4:10166000-10169600	Weak transcription	Right Atrium	heart
9	chr4:10166000-10175400	Weak transcription	Pancreas	Pancrea
10	chr4:10166200-10174000	Weak transcription	Left Ventricle	heart
11	chr4:10166600-10169800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
12	chr4:10167000-10169600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
13	chr4:10167000-10169600	Weak transcription	Fetal Heart	heart
14	chr4:10167000-10172400	Weak transcription	HMEC	breast
15	chr4:10167000-10172600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
16	chr4:10167200-10174400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
17	chr4:10167800-10171400	Genic enhancers	K562	blood
18	chr4:10168400-10170200	Enhancers	Fetal Thymus	thymus
19	chr4:10168400-10170400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
20	chr4:10169200-10171000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
21	chr4:10169200-10173600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
22	chr4:10169400-10169800	Weak transcription	Fetal Intestine Large	intestine
23	chr4:10169400-10170400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
24	chr4:10169600-10170000	Enhancers	Placenta	Placenta
25	chr4:10169600-10170200	Enhancers	Right Atrium	heart
26	chr4:10169600-10170400	Enhancers	Sigmoid Colon	Sigmoid Colon
27	chr4:10169600-10170600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
28	chr4:10169600-10170800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
29	chr4:10169600-10171000	Enhancers	Fetal Heart	heart
30	chr4:10169800-10170200	Enhancers	Primary hematopoietic stem cells short term culture	blood
31	chr4:10169800-10170400	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
32	chr4:10169800-10170400	Enhancers	Fetal Intestine Large	intestine
33	chr4:10169800-10170400	Enhancers	Fetal Intestine Small	intestine
34	chr4:10169800-10173400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
35	chr4:10170000-10170200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
36	chr4:10170000-10170200	Enhancers	Adipose Nuclei	Adipose
37	chr4:10170000-10171600	Weak transcription	Placenta	Placenta
38	chr4:10170200-10174000	Weak transcription	Fetal Thymus	thymus
39	chr4:10170200-10174000	Weak transcription	Right Atrium	heart
40	chr4:10170200-10174200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
41	chr4:10170400-10171400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
42	chr4:10170400-10172400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
43	chr4:10170400-10172600	Weak transcription	Fetal Intestine Large	intestine
44	chr4:10170400-10172600	Weak transcription	Fetal Intestine Small	intestine
45	chr4:10170400-10173800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
46	chr4:10170400-10174000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
47	chr4:10170600-10172600	Weak transcription	Adipose Nuclei	Adipose
48	chr4:10170600-10173600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
49	chr4:10170800-10172400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
50	chr4:10171000-10171400	Weak transcription	Fetal Heart	heart

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