Variant report

Variant	nsv551839
Chromosome Location	chr10:90334835-90422136
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr10:90342487-90343358	GM12878	blood:	n/a	n/a
2	ATF3	chr10:90342497-90342885	GM12878	blood:	n/a	chr10:90342650-90342670 chr10:90342661-90342670
3	ATF3	chr10:90342553-90342782	GM12878	blood:	n/a	chr10:90342650-90342670 chr10:90342661-90342670
4	ATF3	chr10:90342556-90342930	H1-hESC	embryonic stem cell:	n/a	chr10:90342650-90342670 chr10:90342661-90342670
5	ATF3	chr10:90342558-90342841	H1-hESC	embryonic stem cell:	n/a	chr10:90342650-90342670 chr10:90342661-90342670
6	BACH1	chr10:90342738-90343061	H1-hESC	embryonic stem cell:	n/a	n/a
7	BATF	chr10:90367779-90368459	GM12878	blood:	n/a	n/a
8	BATF	chr10:90368087-90368480	GM12878	blood:	n/a	n/a
9	BCL11A	chr10:90367910-90368124	GM12878	blood:	n/a	n/a
10	BCLAF1	chr10:90342505-90343467	GM12878	blood:	n/a	chr10:90343114-90343127
11	BCLAF1	chr10:90357695-90358200	GM12878	blood:	n/a	n/a
12	BHLHE40	chr10:90342352-90343314	GM12878	blood:	n/a	chr10:90342661-90342670 chr10:90342661-90342670 chr10:90342659-90342672 chr10:90342662-90342671
13	BHLHE40	chr10:90343183-90343272	K562	blood:	n/a	n/a
14	BHLHE40	chr10:90367891-90368463	GM12878	blood:	n/a	n/a
15	BHLHE40	chr10:90342539-90342866	K562	blood:	n/a	chr10:90342661-90342670 chr10:90342661-90342670 chr10:90342659-90342672 chr10:90342662-90342671
16	BRCA1	chr10:90401867-90403141	Hela-S3	cervix:	n/a	n/a
17	BRCA1	chr10:90404716-90404862	Hela-S3	cervix:	n/a	n/a
18	BRCA1	chr10:90410717-90411361	Hela-S3	cervix:	n/a	n/a
19	CEBPB	chr10:90358937-90359032	A549	lung:	n/a	n/a
20	CEBPB	chr10:90408798-90408922	Hela-S3	cervix:	n/a	n/a
21	CEBPB	chr10:90408756-90408868	IMR90	lung:	n/a	n/a
22	CEBPB	chr10:90410814-90411177	A549	lung:	n/a	n/a
23	CEBPB	chr10:90380766-90381020	IMR90	lung:	n/a	n/a
24	CEBPB	chr10:90410765-90411472	A549	lung:	n/a	n/a
25	CEBPB	chr10:90410758-90411411	Hela-S3	cervix:	n/a	n/a
26	CEBPB	chr10:90410835-90411199	A549	lung:	n/a	n/a
27	CEBPB	chr10:90402797-90403142	IMR90	lung:	n/a	chr10:90402976-90402989
28	CEBPB	chr10:90401845-90402554	Hela-S3	cervix:	n/a	n/a
29	CEBPB	chr10:90402825-90403140	A549	lung:	n/a	chr10:90402976-90402989
30	CEBPB	chr10:90417750-90418055	IMR90	lung:	n/a	n/a
31	CEBPB	chr10:90419406-90419735	IMR90	lung:	n/a	n/a
32	CEBPB	chr10:90410729-90411362	IMR90	lung:	n/a	n/a
33	CEBPB	chr10:90402768-90403182	Hela-S3	cervix:	n/a	chr10:90402976-90402989
34	CEBPB	chr10:90402871-90403263	A549	lung:	n/a	chr10:90402976-90402989
35	CEBPB	chr10:90402871-90403134	A549	lung:	n/a	chr10:90402976-90402989
36	CHD1	chr10:90342031-90342069	GM12878	blood:	n/a	n/a
37	CHD1	chr10:90342766-90343148	GM12878	blood:	n/a	n/a
38	CHD2	chr10:90342562-90343360	H1-hESC	embryonic stem cell:	n/a	n/a
39	CHD2	chr10:90342545-90343324	GM12878	blood:	n/a	n/a
40	CREB1	chr10:90357833-90358294	GM12878	blood:	n/a	n/a
41	CREB1	chr10:90342493-90343248	H1-hESC	embryonic stem cell:	n/a	n/a
42	CREB1	chr10:90342512-90343170	A549	lung:	n/a	n/a
43	CREB1	chr10:90357784-90358402	GM12878	blood:	n/a	n/a
44	CREB1	chr10:90342484-90343348	H1-hESC	embryonic stem cell:	n/a	n/a
45	CTCF	chr10:90342917-90343225	Lung_OC	lung:	n/a	chr10:90343091-90343109 chr10:90343094-90343107
46	CTCF	chr10:90342952-90343170	HepG2	liver:	n/a	chr10:90343091-90343109 chr10:90343094-90343107
47	CTCF	chr10:90343011-90343174	HepG2	liver:	n/a	chr10:90343091-90343109 chr10:90343094-90343107
48	CTCF	chr10:90343020-90343170	HA-sp	spinal cord:	n/a	chr10:90343091-90343109 chr10:90343094-90343107
49	CTCF	chr10:90343020-90343170	HEEpiC	esophagus:	n/a	chr10:90343091-90343109 chr10:90343094-90343107
50	CTCF	chr10:90342840-90343228	H1-hESC	embryonic stem cell:	n/a	chr10:90343091-90343109 chr10:90343094-90343107

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:90341959-90342009	A549	lung:	n/a
2	chr10:90341959-90342009	A549	lung:	n/a
3	chr10:90343208-90343258	NHBE	bronchial:	n/a
4	chr10:90343435-90343485	MCF-7	breast:	n/a
5	chr10:90345860-90345910	AG04450	lung:	fetal
6	chr10:90346597-90346647	PFSK-1	brain:	n/a
7	chr10:90345860-90345910	K562	blood:	n/a
8	chr10:90339186-90339236	AoSMC	blood vessel:	n/a
9	chr10:90343285-90343335	SK-N-SH_RA	brain:	n/a
10	chr10:90346597-90346647	GM06990	blood:	n/a
11	chr10:90364671-90364721	HPAEpiC	pulmonary alveolar:	n/a
12	chr10:90345356-90345406	SK-N-SH_RA	brain:	n/a
13	chr10:90339186-90339236	GM06990	blood:	n/a
14	chr10:90343166-90343216	HL-60	blood:	n/a
15	chr10:90345170-90345220	H1-hESC	embryonic stem cell:	embryo
16	chr10:90342814-90342864	AG10803	skin:	n/a
17	chr10:90420117-90420167	HRPEpiC	eye:	n/a
18	chr10:90345170-90345220	HRPEpiC	eye:	n/a
19	chr10:90343641-90343691	CMK	blood:	n/a
20	chr10:90343220-90343270	Hepatocyte	liver:	n/a
21	chr10:90343208-90343258	BJ	skin:	n/a
22	chr10:90343641-90343691	ProgFib	skin:	n/a
23	chr10:90345860-90345910	HEEpiC	esophagus:	n/a
24	chr10:90343208-90343258	Caco-2	colon:	n/a
25	chr10:90343435-90343485	Hela-S3	cervix:	n/a
26	chr10:90343641-90343691	Caco-2	colon:	n/a
27	chr10:90346479-90346529	NB4	blood:	n/a
28	chr10:90345170-90345220	Hepatocyte	liver:	n/a
29	chr10:90343174-90343224	AG09309	skin:	n/a
30	chr10:90341959-90342009	NHBE	bronchial:	n/a
31	chr10:90342899-90342949	ProgFib	skin:	n/a
32	chr10:90342899-90342949	GM06990	blood:	n/a
33	chr10:90345356-90345406	SKMC	muscle:	n/a
34	chr10:90342899-90342949	SKMC	muscle:	n/a
35	chr10:90346597-90346647	SK-N-MC	brain:	n/a
36	chr10:90420117-90420167	U87	brain:	n/a
37	chr10:90343192-90343242	AG09309	skin:	n/a
38	chr10:90343192-90343242	HRE	kidney:	n/a
39	chr10:90346479-90346529	BE2_C	brain:	n/a
40	chr10:90343220-90343270	PFSK-1	brain:	n/a
41	chr10:90342738-90342788	AoSMC	blood vessel:	n/a
42	chr10:90346479-90346529	SAEC	small airway:	n/a
43	chr10:90346597-90346647	AG10803	skin:	n/a
44	chr10:90420117-90420167	HAEpiC	amniotic membrane:	n/a
45	chr10:90343641-90343691	ECC-1	luminal epithelium:	n/a
46	chr10:90343174-90343224	AG04450	lung:	fetal
47	chr10:90345170-90345220	HNPCEpiC	eye:	n/a
48	chr10:90343435-90343485	HNPCEpiC	eye:	n/a
49	chr10:90345860-90345910	NHDF-neo	bronchial:	n/a
50	chr10:90345356-90345406	AG04450	lung:	fetal

No.	Distal block	Cell Line	Cell type
1	chr10:89623284..89624802-chr10:90333156..90335627,2	MCF-7	breast:
2	chr10:90363656..90365156-chr2:88314680..88316316,2	MCF-7	breast:
3	chr10:90341555..90343479-chr10:90350862..90352924,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-LIPJ-2	chr10:90343084-90344727	NONHSAT015473
2	lnc-RNLS-2	chr10:90377980-90378691	NONHSAT015476

Variant related genes	Relation type
ENSG00000201548	TF binding region
LIPJ	TF binding region
RNLS	TF binding region
RPL7P34	TF binding region
LIPF	TF binding region
ENSG00000201548	CpG island
LIPJ	CpG island
RNLS	CpG island
RPL7P34	CpG island
LIPF	CpG island
ENSG00000171862	chromatin interactions
ENSG00000222724	chromatin interactions
ENSG00000184719	chromatin interactions

Extended variants
information (count: 1917 )
Associated
traits (count: 95 )

Variant overlapped rSNPs/rCNVs (count:1917 , 50 per page) page: 1 2 3 4 5 6 7 ... 39

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2477958	chr10:90334835-90334836	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs139780037	chr10:90334869-90334870	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs373883273	chr10:90334911-90334912	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs67949156	chr10:90334912-90334913	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs367776961	chr10:90334913-90334914	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs375572767	chr10:90334917-90334918	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs7906052	chr10:90334918-90334919	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs201891717	chr10:90334938-90334939	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs377248573	chr10:90334954-90334955	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs368178662	chr10:90334960-90334961	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs369672109	chr10:90334961-90334962	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs11595396	chr10:90334963-90334964	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs10887833	chr10:90334965-90334966	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs111766573	chr10:90334971-90334972	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs368630535	chr10:90334972-90334973	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs10887834	chr10:90334973-90334974	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs10887835	chr10:90334975-90334976	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs28631536	chr10:90334990-90334991	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs28401683	chr10:90334994-90334995	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs572104128	chr10:90335021-90335022	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs113818151	chr10:90335023-90335024	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs534423514	chr10:90335039-90335040	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs369328719	chr10:90335040-90335041	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs189888859	chr10:90335041-90335042	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs539327791	chr10:90335069-90335070	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs74147234	chr10:90335074-90335075	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs180831992	chr10:90335090-90335091	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs111846521	chr10:90335136-90335137	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs555192612	chr10:90335168-90335169	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs74147235	chr10:90335175-90335176	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs542091636	chr10:90335178-90335179	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs184582751	chr10:90335211-90335212	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs74799701	chr10:90335228-90335229	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs141057449	chr10:90335290-90335291	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs150106030	chr10:90335379-90335380	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs149044736	chr10:90335468-90335469	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs528495366	chr10:90335496-90335497	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs540596926	chr10:90335500-90335501	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs562059992	chr10:90335506-90335507	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs145517823	chr10:90335528-90335529	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs557883256	chr10:90335562-90335563	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs34272895	chr10:90335563-90335564	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs550532753	chr10:90335569-90335570	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs562341213	chr10:90335570-90335571	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs141075827	chr10:90335596-90335597	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs556439241	chr10:90335664-90335665	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs114991483	chr10:90335678-90335679	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs533569112	chr10:90335692-90335693	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs577039173	chr10:90335751-90335752	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs575233749	chr10:90335783-90335784	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:95)

Disease	PMID	Source
Gastric cancer	17908304	CNVD
Chordoma	21602918	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	21979893	CNVD
Melanoma	18172304	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
Ewing''s sarcoma	17952124	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	20724749	CNVD
Autism	22495311	CNVD
Prostate cancer	18632612	CNVD
Cockayne syndrome	18421352	CNVD
Glioblastoma	16823260	CNVD
Medulloblastoma	16968546	CNVD
Neuroblastoma	17533364	CNVD
Squamous cell cancer	21044232	CNVD
Glioma	21971842	CNVD
Cancer	21637783	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Colorectal cancer	20709793	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Lung cancer	18438408	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Usher syndrome	20538994	CNVD
Medulloblastoma	16783165	CNVD
Breast cancer	21785460	CNVD
Acute myeloid leukemia	20729466	CNVD
Prostate cancer	16573809	CNVD
Paraganglioma	17535989	CNVD
Submicroscopic aberration syndrome	21292638	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Pulmonary chondroma	17535989	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Colorectal cancer	18645599	CNVD
Polyposis syndrome	18645599	CNVD
Prostate cancer	17245344	CNVD
Glioblastoma multiforme	17369134	CNVD
Glioblastoma multiforme	21750150	CNVD
Breast cancer	22032731	CNVD
Ovarian cancer	20844748	CNVD
Glioblastoma multiforme	17002787	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	17603634	CNVD
Glioblastoma multiforme	17387387	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Breast cancer	21364760	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Wilms tumour	21544195	CNVD
Cancer	20164919	CNVD
small cell lung cancer	20016488	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Urothelial carcinoma	21177765	CNVD
Cancer	20164920	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Colorectal cancer	19359472	CNVD
Neurocytoma	17123091	CNVD
Prostate cancer	16461572	CNVD
Basal-like breast cancer	18066063	CNVD
Effusion lymphoma	18079361	CNVD
Melanoma	17363583	CNVD
Prostate cancer	21147910	CNVD
Lung cancer	21911935	CNVD
Myelofibrosis	22110671	CNVD
Prostate cancer	21088497	CNVD
Breast cancer	22048815	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Glioblastoma multiforme	22291905	CNVD
Glioblastoma multiforme	19435819	CNVD
Glioblastoma multiforme	22286061	CNVD
Intracranial ependymoma	16609018	CNVD
Breast cancer	16397240	CNVD
Chronic lymphocytic leukemia	21049055	CNVD
Cervical cancer	21062161	CNVD
Non-small cell lung cancer	21829676	CNVD
Melanoma	24453001	CNVD
Breast cancer	16608533	CNVD
Ependymoma	20639864	CNVD
Breast cancer	22522925	CNVD
Bipolar disorder	19114987	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Amyotrophic lateral sclerosis	20685689	CNVD
Pancreatic cancer	17952125	CNVD
T-cell lymphomas	22341440	CNVD
Cancer	17440070	CNVD

Chromatin state (count:518 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:90312200-90342400	Weak transcription	Ovary	ovary
2	chr10:90315400-90342400	Weak transcription	Aorta	Aorta
3	chr10:90317800-90341800	Weak transcription	Adipose Nuclei	Adipose
4	chr10:90319200-90342000	Weak transcription	Pancreas	Pancrea
5	chr10:90321000-90342000	Weak transcription	Duodenum Smooth Muscle	Duodenum
6	chr10:90326800-90342400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
7	chr10:90331000-90341800	Weak transcription	Skeletal Muscle Female	skeletal muscle
8	chr10:90331000-90342400	Weak transcription	Psoas Muscle	Psoas
9	chr10:90331400-90342400	Weak transcription	Left Ventricle	heart
10	chr10:90331600-90342400	Weak transcription	Esophagus	oesophagus
11	chr10:90331800-90342000	Weak transcription	Gastric	stomach
12	chr10:90336200-90337800	Enhancers	Pancreatic Islets	Pancreatic Islet
13	chr10:90337800-90341800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
14	chr10:90337800-90341800	Weak transcription	Pancreatic Islets	Pancreatic Islet
15	chr10:90339600-90342200	Weak transcription	Rectal Mucosa Donor 29	rectum
16	chr10:90340400-90341000	Weak transcription	NHDF-Ad	bronchial
17	chr10:90341800-90342000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
18	chr10:90341800-90342000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
19	chr10:90341800-90342000	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
20	chr10:90341800-90342000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
21	chr10:90341800-90342000	Enhancers	Brain Cingulate Gyrus	brain
22	chr10:90341800-90342000	Enhancers	Pancreatic Islets	Pancreatic Islet
23	chr10:90341800-90342000	Enhancers	Small Intestine	intestine
24	chr10:90341800-90342000	Enhancers	Spleen	Spleen
25	chr10:90341800-90342000	Weak transcription	NHDF-Ad	bronchial
26	chr10:90341800-90342200	Enhancers	Primary T helper naive cells from peripheral blood	blood
27	chr10:90341800-90342200	Enhancers	Adipose Nuclei	Adipose
28	chr10:90341800-90342200	Enhancers	Brain Anterior Caudate	brain
29	chr10:90341800-90342200	Enhancers	Brain Inferior Temporal Lobe	brain
30	chr10:90341800-90342200	Enhancers	Brain Substantia Nigra	brain
31	chr10:90341800-90342200	Enhancers	Colon Smooth Muscle	Colon
32	chr10:90341800-90342200	Enhancers	Osteobl	bone
33	chr10:90341800-90342400	Enhancers	Primary T helper cells PMA-I stimulated	--
34	chr10:90341800-90342400	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
35	chr10:90341800-90342400	Enhancers	Liver	Liver
36	chr10:90341800-90342400	Flanking Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
37	chr10:90341800-90343600	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
38	chr10:90341800-90343800	Active TSS	Skeletal Muscle Female	skeletal muscle
39	chr10:90341800-90343800	Active TSS	Stomach Smooth Muscle	stomach
40	chr10:90342000-90342200	Enhancers	iPS-18 Cell Line	embryonic stem cell
41	chr10:90342000-90342200	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
42	chr10:90342000-90342200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
43	chr10:90342000-90342200	Flanking Active TSS	Duodenum Smooth Muscle	Duodenum
44	chr10:90342000-90342200	Enhancers	Fetal Brain Female	brain
45	chr10:90342000-90342200	Enhancers	Gastric	stomach
46	chr10:90342000-90342200	Enhancers	NHDF-Ad	bronchial
47	chr10:90342000-90342400	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
48	chr10:90342000-90342400	Enhancers	Primary T helper naive cells fromperipheralblood	blood
49	chr10:90342000-90342400	Enhancers	Primary T helper cells fromperipheralblood	blood
50	chr10:90342000-90342400	Enhancers	Primary T killer naive cells fromperipheralblood	blood

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