Variant report

Variant	nsv1037404
Chromosome Location	chr10:428193-467917
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:432)
CpG islands
(count:3845)
Chromatin interactive
region (count:21)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:1)

(count:432 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BCL3	chr10:457507-457860	GM12878	blood:	n/a	chr10:457805-457812
2	BCL3	chr10:457469-457868	GM12878	blood:	n/a	chr10:457805-457812
3	BHLHE40	chr10:463351-463604	K562	blood:	n/a	chr10:463495-463516 chr10:463499-463512
4	BHLHE40	chr10:462084-462386	K562	blood:	n/a	n/a
5	BHLHE40	chr10:441786-441817	GM12878	blood:	n/a	n/a
6	BHLHE40	chr10:434185-434571	HepG2	liver:	n/a	n/a
7	BHLHE40	chr10:434271-434474	HepG2	liver:	n/a	n/a
8	BHLHE40	chr10:443592-443640	GM12878	blood:	n/a	n/a
9	BHLHE40	chr10:434285-434521	HepG2	liver:	n/a	n/a
10	CEBPB	chr10:450132-450673	IMR90	lung:	n/a	n/a
11	CEBPB	chr10:439635-439740	K562	blood:	n/a	n/a
12	CEBPB	chr10:440489-440526	K562	blood:	n/a	n/a
13	CEBPB	chr10:440151-440583	H1-hESC	embryonic stem cell:	n/a	n/a
14	CEBPB	chr10:434271-434623	HepG2	liver:	n/a	chr10:434443-434454
15	CEBPB	chr10:440486-440520	A549	lung:	n/a	n/a
16	CEBPB	chr10:440178-440611	HepG2	liver:	n/a	n/a
17	CEBPB	chr10:434368-434546	HepG2	liver:	n/a	chr10:434443-434454
18	CHD2	chr10:461975-462254	H1-hESC	embryonic stem cell:	n/a	n/a
19	CTCF	chr10:461960-462110	HMF	breast:	n/a	n/a
20	CTCF	chr10:461982-462298	GM12878	blood:	n/a	chr10:462136-462154 chr10:462138-462159 chr10:462139-462152
21	CTCF	chr10:445140-445168	Hela-S3	cervix:	n/a	n/a
22	CTCF	chr10:440239-440325	GM13976	blood:	n/a	n/a
23	CTCF	chr10:462005-462312	MCF-7	breast:	n/a	chr10:462136-462154 chr10:462138-462159 chr10:462139-462152
24	CTCF	chr10:443508-443677	GM12892	blood:	n/a	n/a
25	CTCF	chr10:440494-440640	MCF-7	breast:	n/a	n/a
26	CTCF	chr10:445040-445190	MCF-7	breast:	n/a	n/a
27	CTCF	chr10:462015-462278	H1-hESC	embryonic stem cell:	n/a	chr10:462136-462154 chr10:462138-462159 chr10:462139-462152
28	CTCF	chr10:462000-462150	HA-sp	spinal cord:	n/a	n/a
29	CTCF	chr10:462036-462229	A549	lung:	n/a	chr10:462136-462154 chr10:462138-462159 chr10:462139-462152
30	CTCF	chr10:431634-431780	H1-hESC	embryonic stem cell:	n/a	chr10:431677-431690
31	CTCF	chr10:440260-440410	GM12875	blood:	n/a	n/a
32	CTCF	chr10:462040-462190	GM12878	blood:	n/a	chr10:462136-462154 chr10:462138-462159 chr10:462139-462152
33	CTCF	chr10:462220-462370	A549	lung:	n/a	n/a
34	CTCF	chr10:445114-445208	K562	blood:	n/a	n/a
35	CTCF	chr10:463767-463960	GM10266	blood:	n/a	n/a
36	CTCF	chr10:443501-443668	MCF-7	breast:	n/a	n/a
37	CTCF	chr10:467320-467470	HCPEpiC	choroid plexus:	n/a	chr10:467342-467363 chr10:467347-467365
38	CTCF	chr10:441491-441638	GM12878	blood:	n/a	n/a
39	CTCF	chr10:462020-462170	AoAF	blood vessel:	n/a	chr10:462136-462154 chr10:462138-462159 chr10:462139-462152
40	CTCF	chr10:440624-440687	Pancreas_OC	pancreas:	n/a	n/a
41	CTCF	chr10:445080-445230	HepG2	liver:	n/a	n/a
42	CTCF	chr10:462040-462190	GM12867	blood:	n/a	chr10:462136-462154 chr10:462138-462159 chr10:462139-462152
43	CTCF	chr10:463800-463950	HEK293	kidney:	n/a	n/a
44	CTCF	chr10:434280-434430	Caco-2	colon:	n/a	chr10:434379-434387
45	CTCF	chr10:462040-462190	GM12868	blood:	n/a	chr10:462136-462154 chr10:462138-462159 chr10:462139-462152
46	CTCF	chr10:462067-462211	Hela-S3	cervix:	n/a	chr10:462136-462154 chr10:462138-462159 chr10:462139-462152
47	CTCF	chr10:462200-462350	HAc	cerebellar:	n/a	n/a
48	CTCF	chr10:467249-467462	HUVEC	blood vessel:	n/a	chr10:467342-467363 chr10:467347-467365
49	CTCF	chr10:445149-445184	MCF-7	breast:	n/a	n/a
50	CTCF	chr10:443506-443507	GM12892	blood:	n/a	n/a

(count:3845 , 50 per page) page: 1 2 3 4 5 6 7 ... 77

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:461847-461897	HNPCEpiC	eye:	n/a
2	chr10:465584-465634	ovcar-3	ovarian:	n/a
3	chr10:461847-461897	HNPCEpiC	eye:	n/a
4	chr10:465584-465634	ovcar-3	ovarian:	n/a
5	chr10:443029-443079	HCM	heart:	n/a
6	chr10:443029-443079	SK-N-SH_RA	brain:	n/a
7	chr10:453118-453168	HRPEpiC	eye:	n/a
8	chr10:436626-436676	LNCaP	prostate:	n/a
9	chr10:431095-431145	LNCaP	prostate:	n/a
10	chr10:459697-459747	NH-A	brain:	n/a
11	chr10:435744-435794	AG09319	gingival:	n/a
12	chr10:466825-466875	HAEpiC	amniotic membrane:	n/a
13	chr10:466878-466928	MCF10A-Er-Src	breast:	n/a
14	chr10:461992-462042	GM12878	blood:	n/a
15	chr10:465366-465416	HRPEpiC	eye:	n/a
16	chr10:464965-465015	GM06990	blood:	n/a
17	chr10:466232-466282	AG04449	skin:	fetal
18	chr10:459908-459958	ovcar-3	ovarian:	n/a
19	chr10:464225-464275	HNPCEpiC	eye:	n/a
20	chr10:433089-433139	HRE	kidney:	n/a
21	chr10:465796-465846	HCPEpiC	choroid plexus:	n/a
22	chr10:429943-429993	GM12891	blood:	n/a
23	chr10:461847-461897	HEEpiC	esophagus:	n/a
24	chr10:464965-465015	Caco-2	colon:	n/a
25	chr10:443029-443079	GM12878	blood:	n/a
26	chr10:465796-465846	AG09309	skin:	n/a
27	chr10:453318-453368	GM12891	blood:	n/a
28	chr10:467839-467889	T-47D	breast:	n/a
29	chr10:431934-431984	HPAEpiC	pulmonary alveolar:	n/a
30	chr10:431491-431541	ovcar-3	ovarian:	n/a
31	chr10:441309-441359	A549	lung:	n/a
32	chr10:465366-465416	PANC-1	pancreas:	n/a
33	chr10:438661-438711	HL-60	blood:	n/a
34	chr10:463644-463694	NB4	blood:	n/a
35	chr10:429979-430029	SK-N-MC	brain:	n/a
36	chr10:464452-464502	GM12891	blood:	n/a
37	chr10:438227-438277	IMR90	lung:	fetal
38	chr10:466232-466282	HMEC	breast:	n/a
39	chr10:467839-467889	SK-N-SH_RA	brain:	n/a
40	chr10:464042-464092	A549	lung:	n/a
41	chr10:436477-436527	HepG2	liver:	n/a
42	chr10:467839-467889	HCT-116	colon:	n/a
43	chr10:438517-438567	HNPCEpiC	eye:	n/a
44	chr10:458528-458578	NHDF-neo	bronchial:	n/a
45	chr10:464965-465015	NB4	blood:	n/a
46	chr10:464452-464502	NB4	blood:	n/a
47	chr10:432066-432116	AG09319	gingival:	n/a
48	chr10:435953-436003	ovcar-3	ovarian:	n/a
49	chr10:445130-445180	HUVEC	blood vessel:	n/a
50	chr10:466825-466875	A549	lung:	n/a

(count:21 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr10:382961..385780-chr10:450030..452279,2	MCF-7	breast:
2	chr10:461824..462560-chr10:834643..835579,2	MCF-7	breast:
3	chr10:450870..453541-chr10:454338..458477,5	MCF-7	breast:
4	chr10:415244..418215-chr10:463219..466142,2	MCF-7	breast:
5	chr10:461858..462407-chr10:481646..482609,2	MCF-7	breast:
6	chr10:454564..456430-chr10:464308..466702,2	MCF-7	breast:
7	chr10:460256..464183-chr10:464558..467613,6	MCF-7	breast:
8	chr10:461634..462240-chr10:481924..482823,2	MCF-7	breast:
9	chr10:454564..456430-chr10:464308..466702,2	MCF-7	breast:
10	chr10:461373..464644-chr10:474177..477326,3	MCF-7	breast:
11	chr10:456178..457890-chr10:852622..854288,2	MCF-7	breast:
12	chr10:461779..462665-chr10:840464..841138,2	MCF-7	breast:
13	chr10:460256..464183-chr10:464558..467613,6	MCF-7	breast:
14	chr10:450799..453680-chr10:480575..483479,3	MCF-7	breast:
15	chr10:429914..432466-chr10:434304..435827,2	MCF-7	breast:
16	chr10:414936..417865-chr10:461204..463108,2	MCF-7	breast:
17	chr10:429914..432466-chr10:434304..435827,2	MCF-7	breast:
18	chr10:432437..434689-chr10:436427..439345,2	MCF-7	breast:
19	chr10:450870..453541-chr10:454338..458477,5	MCF-7	breast:
20	chr10:426509..428082-chr10:439441..441586,2	MCF-7	breast:
21	chr10:460205..463295-chr10:478508..482551,4	MCF-7	breast:

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	DIP2C	hsa-miR-335-5p	chr10:428374-428397

Variant related genes	Relation type
DIP2C	TF binding region
DIP2C	CpG island
ENSG00000239822	chromatin interactions
ENSG00000151240	chromatin interactions

Extended variants
information (count: 2489 )
Associated
traits (count: 55 )

Variant overlapped rSNPs/rCNVs (count:2489 , 50 per page) page: 1 2 3 4 5 6 7 ... 50

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs549795202	chr10:428199-428200	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs564735775	chr10:428205-428206	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs575285661	chr10:428231-428232	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs184532081	chr10:428280-428281	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs148263257	chr10:428281-428282	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs530346108	chr10:428282-428283	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs540469824	chr10:428299-428300	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs141280609	chr10:428331-428332	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs111623268	chr10:428351-428352	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs77449932	chr10:428366-428367	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs530266345	chr10:428382-428383	Weak transcription Strong transcription Genic enhancers Enhancers	miRNA target site	1 gene(s)	Overlapped CNVs	n/a
12	rs79643961	chr10:428383-428384	Weak transcription Strong transcription Genic enhancers Enhancers	miRNA target site	1 gene(s)	Overlapped CNVs	n/a
13	rs113779520	chr10:428389-428390	Weak transcription Strong transcription Genic enhancers Enhancers	miRNA target site	1 gene(s)	Overlapped CNVs	n/a
14	rs189307199	chr10:428420-428421	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs565754595	chr10:428437-428438	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs200361132	chr10:428447-428448	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs536087650	chr10:428463-428464	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs150344966	chr10:428479-428480	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs367916470	chr10:428482-428483	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs4881200	chr10:428503-428504	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs180809240	chr10:428523-428524	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs137969620	chr10:428530-428531	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs368101108	chr10:428556-428557	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs372202240	chr10:428564-428565	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs374887683	chr10:428565-428566	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs369283403	chr10:428575-428576	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs148470628	chr10:428601-428602	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs142691003	chr10:428616-428617	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs202022109	chr10:428652-428653	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs372296939	chr10:428655-428656	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs150975809	chr10:428660-428661	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs140993934	chr10:428679-428680	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs199979813	chr10:428709-428710	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs200912485	chr10:428717-428718	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs375412200	chr10:428743-428744	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs368710374	chr10:428745-428746	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs41289249	chr10:428764-428765	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs373187934	chr10:428767-428768	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs75275792	chr10:428781-428782	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs142448956	chr10:428816-428817	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs145957260	chr10:428943-428944	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs556534999	chr10:428971-428972	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs546193377	chr10:428984-428985	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs371559919	chr10:428986-428987	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs374880310	chr10:428996-428997	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs112207122	chr10:429020-429021	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs74786061	chr10:429059-429060	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs568254073	chr10:429078-429079	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs527791953	chr10:429109-429110	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs576765567	chr10:429130-429131	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:55)

Disease	PMID	Source
Cancer	20164920	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	20409316	CNVD
Gastric adenocarcinoma	19115996	CNVD
Pilocytic astrocytoma	18622384	CNVD
Pilomyxoid astrocytoma	18622384	CNVD
Breast cancer	17133270	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Cancer	21129771	CNVD
Sudden cardiac death	19188705	CNVD
Digeorge syndrome	22283845	CNVD
Colorectal cancer	20709793	CNVD
Wilms tumour	19047088	CNVD
Hepatocellular carcinoma	16750200	CNVD
Acute myeloid leukemia	16864856	CNVD
Cancer	21183584	CNVD
Barakat syndrome	22470819	CNVD
Melanoma	18172304	CNVD
Ovarian cancer	21720365	CNVD
Autism	18414403	CNVD
Malignant melanoma	18718029	CNVD
Breast cancer	22032731	CNVD
Medulloblastoma	16783165	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	17603634	CNVD
Endometrial cancer	22040021	CNVD
Glioblastoma multiforme	21080181	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Phyllodes tumor	17334353	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Gastric cancer	17908304	CNVD
Chordoma	21602918	CNVD
Ewing''s sarcoma	21437220	CNVD
Medulloblastoma	21979893	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Melanoma	17363583	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Ewing''s sarcoma	17952124	CNVD
Oral cancer	21386901	CNVD
Breast cancer	21785460	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Breast cancer	21509527	CNVD
Prostate cancer	18632612	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Glioblastoma multiforme	21525872	CNVD
Breast cancer	22522925	CNVD
Breast cancer	21858162	CNVD
Obesity	19966786	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:1220 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:383800-433000	Weak transcription	HUES48 Cell Line	embryonic stem cell
2	chr10:394600-435400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
3	chr10:395800-489400	Weak transcription	Stomach Mucosa	stomach
4	chr10:399000-428400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
5	chr10:408800-435400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
6	chr10:409200-428200	Weak transcription	HUES64 Cell Line	embryonic stem cell
7	chr10:414800-435400	Weak transcription	H1 Cell Line	embryonic stem cell
8	chr10:415600-453800	Weak transcription	Primary T helper cells fromperipheralblood	blood
9	chr10:418400-458400	Weak transcription	Small Intestine	intestine
10	chr10:419000-436000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
11	chr10:419800-435400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
12	chr10:420000-435400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
13	chr10:420000-442600	Weak transcription	Psoas Muscle	Psoas
14	chr10:420200-453200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
15	chr10:420600-432800	Strong transcription	Fetal Muscle Trunk	muscle
16	chr10:420600-433200	Strong transcription	Fetal Muscle Leg	muscle
17	chr10:420600-446200	Strong transcription	Fetal Stomach	stomach
18	chr10:420800-437000	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
19	chr10:421000-437600	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
20	chr10:421200-437600	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
21	chr10:421400-428200	Weak transcription	NH-A	brain
22	chr10:421600-430600	Strong transcription	Foreskin Melanocyte Primary Cells skin01	Skin
23	chr10:421600-436000	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
24	chr10:421600-461800	Weak transcription	A549	lung
25	chr10:421800-432400	Strong transcription	Brain Hippocampus Middle	brain
26	chr10:421800-440200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
27	chr10:422000-437800	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
28	chr10:422800-428400	Strong transcription	Gastric	stomach
29	chr10:422800-438200	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
30	chr10:423200-428600	Strong transcription	Foreskin Fibroblast Primary Cells skin02	Skin
31	chr10:423200-436400	Strong transcription	Brain Substantia Nigra	brain
32	chr10:423200-436400	Strong transcription	HSMMtube	muscle
33	chr10:423400-436200	Weak transcription	Primary T helper cells PMA-I stimulated	--
34	chr10:423600-480200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
35	chr10:424000-429400	Strong transcription	NHDF-Ad	bronchial
36	chr10:424000-433400	Strong transcription	Brain Anterior Caudate	brain
37	chr10:424000-436600	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
38	chr10:424000-436800	Strong transcription	Skeletal Muscle Female	skeletal muscle
39	chr10:424000-437000	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
40	chr10:424000-437000	Strong transcription	Brain Inferior Temporal Lobe	brain
41	chr10:424200-429000	Strong transcription	Pancreas	Pancrea
42	chr10:424200-433000	Strong transcription	Adipose Nuclei	Adipose
43	chr10:424200-433400	Strong transcription	Brain Angular Gyrus	brain
44	chr10:424200-434200	Strong transcription	Brain Cingulate Gyrus	brain
45	chr10:424200-437000	Weak transcription	Primary B cells from peripheral blood	blood
46	chr10:424400-428600	Strong transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
47	chr10:424400-433400	Strong transcription	Brain Dorsolateral Prefrontal Cortex	brain
48	chr10:424400-436800	Strong transcription	Brain Germinal Matrix	brain
49	chr10:424600-428200	Weak transcription	Sigmoid Colon	Sigmoid Colon
50	chr10:424600-437800	Strong transcription	Cortex derived primary cultured neurospheres	brain

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