Variant report

Variant	nsv548397
Chromosome Location	chr1:185104842-185123630
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:152)
CpG islands
(count:61)
Chromatin interactive
region (count:31)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:152 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:185120426-185120752	K562	blood:	n/a	n/a
2	CEBPB	chr1:185114410-185114717	K562	blood:	n/a	chr1:185114557-185114568 chr1:185114555-185114568 chr1:185114555-185114568
3	CTCF	chr1:185123020-185123170	GM12865	blood:	n/a	n/a
4	CTCF	chr1:185122960-185123110	HVMF	connective:	n/a	n/a
5	CTCF	chr1:185123143-185123167	Medullo	brain:	n/a	n/a
6	CTCF	chr1:185123140-185123290	HRPEpiC	eye:	n/a	n/a
7	CTCF	chr1:185123100-185123250	NHLF	lung:	n/a	n/a
8	CTCF	chr1:185123063-185123241	A549	lung:	n/a	n/a
9	CTCF	chr1:185123080-185123230	GM12867	blood:	n/a	n/a
10	CTCF	chr1:185123060-185123210	HRE	kidney:	n/a	n/a
11	CTCF	chr1:185123100-185123250	GM12872	blood:	n/a	n/a
12	CTCF	chr1:185123080-185123230	HMEC	breast:	n/a	n/a
13	CTCF	chr1:185122990-185123350	GM12878	blood:	n/a	n/a
14	CTCF	chr1:185123140-185123290	AG09319	gingival:	n/a	n/a
15	CTCF	chr1:185123100-185123250	GM12866	blood:	n/a	n/a
16	CTCF	chr1:185123100-185123250	GM12878	blood:	n/a	n/a
17	CTCF	chr1:185123142-185123231	GM12878	blood:	n/a	n/a
18	CTCF	chr1:185123040-185123190	GM12869	blood:	n/a	n/a
19	CTCF	chr1:185122995-185123367	K562	blood:	n/a	n/a
20	CTCF	chr1:185123160-185123310	BE2_C	brain:	n/a	n/a
21	CTCF	chr1:185123060-185123210	HCPEpiC	choroid plexus:	n/a	n/a
22	CTCF	chr1:185123080-185123230	K562	blood:	n/a	n/a
23	CTCF	chr1:185123120-185123270	GM12801	blood:	n/a	n/a
24	CTCF	chr1:185123100-185123250	HBMEC	blood vessel:	n/a	n/a
25	CTCF	chr1:185123160-185123310	A549	lung:	n/a	n/a
26	CTCF	chr1:185123080-185123230	HPAF	blood vessel:	n/a	n/a
27	CTCF	chr1:185123040-185123190	NHDF-neo	bronchial:	n/a	n/a
28	CTCF	chr1:185123110-185123220	GM13976	blood:	n/a	n/a
29	CTCF	chr1:185123040-185123190	HCT-116	colon:	n/a	n/a
30	CTCF	chr1:185123082-185123245	K562	blood:	n/a	n/a
31	CTCF	chr1:185123120-185123270	AG10803	skin:	n/a	n/a
32	CTCF	chr1:185123080-185123230	SK-N-SH_RA	brain:	n/a	n/a
33	CTCF	chr1:185123140-185123224	Spleen_OC	spleen:	n/a	n/a
34	CTCF	chr1:185123060-185123210	HMEC	breast:	n/a	n/a
35	CTCF	chr1:185123120-185123270	GM12873	blood:	n/a	n/a
36	CTCF	chr1:185123113-185123187	GM13977	blood:	n/a	n/a
37	CTCF	chr1:185123060-185123210	RPTEC	kidney:	n/a	n/a
38	CTCF	chr1:185123100-185123250	GM12873	blood:	n/a	n/a
39	CTCF	chr1:185123080-185123230	GM12875	blood:	n/a	n/a
40	CTCF	chr1:185123080-185123230	GM12864	blood:	n/a	n/a
41	CTCF	chr1:185122960-185123110	HFF-Myc	foreskin:	n/a	n/a
42	CTCF	chr1:185123060-185123210	SK-N-SH_RA	brain:	n/a	n/a
43	CTCF	chr1:185123140-185123290	HA-sp	spinal cord:	n/a	n/a
44	CTCF	chr1:185123120-185123270	NB4	blood:	n/a	n/a
45	CTCF	chr1:185123100-185123250	HFF	foreskin:	n/a	n/a
46	CTCF	chr1:185122900-185123050	HCT-116	colon:	n/a	n/a
47	CTCF	chr1:185123098-185123239	Hela-S3	cervix:	n/a	n/a
48	CTCF	chr1:185123140-185123290	GM06990	blood:	n/a	n/a
49	CTCF	chr1:185123040-185123190	AG04450	lung:	n/a	n/a
50	CTCF	chr1:185123089-185123190	HepG2	liver:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:185113945-185113995	Hela-S3	cervix:	n/a
2	chr1:185113945-185113995	MCF10A-Er-Src	breast:	n/a
3	chr1:185113945-185113995	AG09309	skin:	n/a
4	chr1:185113945-185113995	NT2-D1	testis:	n/a
5	chr1:185113945-185113995	GM06990	blood:	n/a
6	chr1:185113945-185113995	RPTEC	kidney:	n/a
7	chr1:185113945-185113995	SAEC	small airway:	n/a
8	chr1:185113945-185113995	AG10803	skin:	n/a
9	chr1:185113945-185113995	HCF	heart:	n/a
10	chr1:185113945-185113995	HRCEpiC	kidney:	n/a
11	chr1:185113945-185113995	HEEpiC	esophagus:	n/a
12	chr1:185113945-185113995	HEK293	kidney:	embryo
13	chr1:185113945-185113995	BJ	skin:	n/a
14	chr1:185113945-185113995	HUVEC	blood vessel:	n/a
15	chr1:185113945-185113995	AG04449	skin:	fetal
16	chr1:185113945-185113995	HCPEpiC	choroid plexus:	n/a
17	chr1:185113945-185113995	NHBE	bronchial:	n/a
18	chr1:185113945-185113995	HCM	heart:	n/a
19	chr1:185113945-185113995	HRPEpiC	eye:	n/a
20	chr1:185113945-185113995	HL-60	blood:	n/a
21	chr1:185113945-185113995	Caco-2	colon:	n/a
22	chr1:185113945-185113995	PrEC	prostate:	n/a
23	chr1:185113945-185113995	NHDF-neo	bronchial:	n/a
24	chr1:185113945-185113995	Jurkat	blood:	n/a
25	chr1:185113945-185113995	SKMC	muscle:	n/a
26	chr1:185113945-185113995	NH-A	brain:	n/a
27	chr1:185113945-185113995	AG04450	lung:	fetal
28	chr1:185113945-185113995	SK-N-SH	brain:	n/a
29	chr1:185113945-185113995	LNCaP	prostate:	n/a
30	chr1:185113945-185113995	HPAEpiC	pulmonary alveolar:	n/a
31	chr1:185113945-185113995	SK-N-SH_RA	brain:	n/a
32	chr1:185113945-185113995	CMK	blood:	n/a
33	chr1:185113945-185113995	HRE	kidney:	n/a
34	chr1:185113945-185113995	IMR90	lung:	fetal
35	chr1:185113945-185113995	PFSK-1	brain:	n/a
36	chr1:185113945-185113995	SK-N-MC	brain:	n/a
37	chr1:185113945-185113995	HAEpiC	amniotic membrane:	n/a
38	chr1:185113945-185113995	H1-hESC	embryonic stem cell:	embryo
39	chr1:185113945-185113995	HepG2	liver:	n/a
40	chr1:185113945-185113995	ovcar-3	ovarian:	n/a
41	chr1:185113945-185113995	NB4	blood:	n/a
42	chr1:185113945-185113995	MCF-7	breast:	n/a
43	chr1:185113945-185113995	GM12891	blood:	n/a
44	chr1:185113945-185113995	GM12892	blood:	n/a
45	chr1:185113945-185113995	K562	blood:	n/a
46	chr1:185113945-185113995	U87	brain:	n/a
47	chr1:185113945-185113995	GM12878	blood:	n/a
48	chr1:185113945-185113995	AoSMC	blood vessel:	n/a
49	chr1:185113945-185113995	T-47D	breast:	n/a
50	chr1:185113945-185113995	ECC-1	luminal epithelium:	n/a

(count:31 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:185104278..185107115-chr1:185121320..185123089,2	K562	blood:
2	chr1:185121566..185123829-chr1:185138646..185140537,2	K562	blood:
3	chr1:185115388..185115967-chr12:81272400..81273262,2	MCF-7	breast:
4	chr1:185122329..185126145-chr1:185137203..185141899,4	K562	blood:
5	chr1:185097360..185099907-chr1:185110020..185112748,3	K562	blood:
6	chr1:185110219..185112548-chr1:185124480..185127523,3	MCF-7	breast:
7	chr1:185104278..185107115-chr1:185121320..185123089,2	K562	blood:
8	chr1:185122996..185124550-chr1:185124586..185126416,2	K562	blood:
9	chr1:185118743..185122593-chr1:185123034..185127983,12	K562	blood:
10	chr1:185118825..185122081-chr1:185134391..185138048,3	K562	blood:
11	chr1:185114068..185116270-chr1:185124385..185126877,5	MCF-7	breast:
12	chr1:185112895..185116881-chr1:185123287..185126781,5	K562	blood:
13	chr1:185013290..185015307-chr1:185120002..185123053,3	MCF-7	breast:
14	chr1:185116622..185122065-chr1:185122168..185128175,9	MCF-7	breast:
15	chr1:185113029..185115978-chr1:185116966..185118773,2	K562	blood:
16	chr1:185122925..185124653-chr20:52755101..52757157,2	MCF-7	breast:
17	chr1:185111010..185114000-chr1:185116930..185118963,2	MCF-7	breast:
18	chr1:185112945..185115248-chr1:185120909..185123637,2	MCF-7	breast:
19	chr1:185113319..185116352-chr1:185124187..185127216,4	MCF-7	breast:
20	chr1:185112945..185115248-chr1:185120909..185123637,2	MCF-7	breast:
21	chr1:185014501..185017888-chr1:185123055..185126846,5	MCF-7	breast:
22	chr1:185099798..185103088-chr1:185104012..185107773,3	K562	blood:
23	chr1:185035986..185038971-chr1:185111907..185115590,3	MCF-7	breast:
24	chr1:185012738..185017820-chr1:185123187..185127311,9	K562	blood:
25	chr1:185114176..185116855-chr1:185120494..185122664,2	K562	blood:
26	chr1:185014410..185016846-chr1:185107860..185109945,2	K562	blood:
27	chr1:185073065..185075023-chr1:185121004..185123409,2	MCF-7	breast:
28	chr1:185111010..185114000-chr1:185116930..185118963,2	MCF-7	breast:
29	chr1:185014401..185016308-chr1:185117123..185120089,2	MCF-7	breast:
30	chr1:185113029..185115978-chr1:185116966..185118773,2	K562	blood:
31	chr1:185114176..185116855-chr1:185120494..185122664,2	K562	blood:

No data

Variant related genes	Relation type
TRMT1L	TF binding region
SWT1	TF binding region
TRMT1L	CpG island
SWT1	CpG island
ENSG00000116668	chromatin interactions
ENSG00000121481	chromatin interactions
ENSG00000121486	chromatin interactions
ENSG00000231084	chromatin interactions

Extended variants
information (count: 691 )
Associated
traits (count: 92 )

Variant overlapped rSNPs/rCNVs (count:691 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6685215	chr1:185104842-185104843	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs545562735	chr1:185104867-185104868	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs563763974	chr1:185104885-185104886	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs530621686	chr1:185104898-185104899	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs548853236	chr1:185104953-185104954	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs187676173	chr1:185104974-185104975	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs191754070	chr1:185105003-185105004	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs575807201	chr1:185105207-185105208	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs367848383	chr1:185105227-185105228	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs546471929	chr1:185105309-185105310	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs544735232	chr1:185105313-185105314	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs184006864	chr1:185105353-185105354	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs188692869	chr1:185105369-185105370	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs370453590	chr1:185105398-185105399	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs565041887	chr1:185105424-185105425	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs550712850	chr1:185105433-185105434	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs78034856	chr1:185105486-185105487	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs537551469	chr1:185105512-185105513	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs150999409	chr1:185105518-185105519	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs11806751	chr1:185105544-185105545	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs536343145	chr1:185105551-185105552	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs192586008	chr1:185105553-185105554	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs370578414	chr1:185105563-185105564	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs553426048	chr1:185105567-185105568	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs578241269	chr1:185105618-185105619	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs184488823	chr1:185105621-185105622	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs557481181	chr1:185105662-185105663	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs575793604	chr1:185105684-185105685	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs542695416	chr1:185105744-185105745	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs560681551	chr1:185105753-185105754	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs528052248	chr1:185105774-185105775	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs190543044	chr1:185105787-185105788	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs547866683	chr1:185105812-185105813	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs532391895	chr1:185105855-185105856	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs550649586	chr1:185105858-185105859	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs12404644	chr1:185105892-185105893	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs529882620	chr1:185105912-185105913	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs549478134	chr1:185105933-185105934	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs182324241	chr1:185105945-185105946	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs186922790	chr1:185105948-185105949	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs535138274	chr1:185105960-185105961	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs726335	chr1:185106004-185106005	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs188774333	chr1:185106017-185106018	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs5779243	chr1:185106126-185106127	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs539314577	chr1:185106131-185106132	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs541080390	chr1:185106169-185106170	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs1407554	chr1:185106267-185106268	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs181554553	chr1:185106297-185106298	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs544126827	chr1:185106315-185106316	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs570232417	chr1:185106321-185106322	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:92)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Autism	22495311	CNVD
Liposarcoma	21253554	CNVD
Burkitt''s lymphoma	18698080	CNVD
Melanoma	18172304	CNVD
Rett syndrome	21593744	CNVD
Cancer	20164919	CNVD
Medulloblastoma	21979893	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Non-small cell lung cancer	21044232	CNVD
Cervical cancer	21063398	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	20632083	CNVD
Endometrial cancer	22040021	CNVD
Ewing''s sarcoma	21437220	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	21080181	CNVD
Hepatocellular carcinoma	22174799	CNVD
Medulloblastoma	21292688	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	21264507	CNVD
Multiple myeloma	21628407	CNVD
Cancer	16751803	CNVD
Prostate cancer	16705090	CNVD
Neuroblastoma	19435921	CNVD
Breast cancer	17850661	CNVD
Breast cancer	16461572	CNVD
Intracranial tumor	16823260	CNVD
Medulloblastoma	18056178	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Colorectal cancer	16272173	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Neuroblastoma	21899760	CNVD
Bladder cancer	19088036	CNVD
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17002787	CNVD
Breast cancer	21858162	CNVD
Non-small cell lung cancer	21385341	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	16608533	CNVD
Ewing''s sarcoma	22429812	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Hepatocellular carcinoma	18803288	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17001317	CNVD
Urothelial carcinoma	21177765	CNVD
Acute myeloid leukemia	21251322	CNVD
Multiple myeloma	17550852	CNVD
Prostate cancer	18632612	CNVD
Acute myeloid leukemia	20729466	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Testicular germ cell tumor	18059402	CNVD
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
Neuroblastoma	18923191	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Ewing''s sarcoma	17952124	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Hepatocellular carcinoma	16750200	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21509527	CNVD
Glioblastoma multiforme	17369134	CNVD
Cancer	17440070	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Metanephric adenoma	20802469	CNVD
Renal cell carcinoma	18765545	CNVD
Nephroblastoma	17189400	CNVD
Melanoma	20688739	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21611746	CNVD
Myelofibrosis	22110671	CNVD
primary effusion lymphomas	17116491	CNVD
Breast cancer	17393978	CNVD
Barrett''s syndrome	19417022	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Breast cancer	22522925	CNVD
Schizophrenia	19197363	CNVD

Chromatin state (count:581 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:185056200-185124200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
2	chr1:185059000-185124800	Weak transcription	H9 Cell Line	embryonic stem cell
3	chr1:185068400-185110200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
4	chr1:185073600-185115000	Weak transcription	NH-A	brain
5	chr1:185082600-185125400	Weak transcription	Spleen	Spleen
6	chr1:185084200-185124400	Weak transcription	Right Ventricle	heart
7	chr1:185085000-185121400	Weak transcription	NHEK	skin
8	chr1:185085400-185125000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
9	chr1:185086000-185107000	Strong transcription	Liver	Liver
10	chr1:185086000-185120200	Strong transcription	Primary neutrophils fromperipheralblood	blood
11	chr1:185087000-185125000	Weak transcription	Gastric	stomach
12	chr1:185087600-185117000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
13	chr1:185088000-185107800	Strong transcription	Primary T helper cells fromperipheralblood	blood
14	chr1:185088200-185120600	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
15	chr1:185088600-185106400	Strong transcription	Primary T helper cells PMA-I stimulated	--
16	chr1:185089400-185124400	Weak transcription	Colonic Mucosa	Colon
17	chr1:185089600-185121400	Weak transcription	Stomach Mucosa	stomach
18	chr1:185091200-185121400	Weak transcription	Fetal Heart	heart
19	chr1:185093800-185113400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
20	chr1:185093800-185117400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
21	chr1:185094000-185110800	Weak transcription	Brain Angular Gyrus	brain
22	chr1:185094000-185113000	Weak transcription	Colon Smooth Muscle	Colon
23	chr1:185094200-185116600	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
24	chr1:185094200-185118400	Weak transcription	H1 Cell Line	embryonic stem cell
25	chr1:185096600-185121400	Weak transcription	Hela-S3	cervix
26	chr1:185100000-185110800	Weak transcription	NHLF	lung
27	chr1:185100400-185105600	Strong transcription	HUES6 Cell Line	embryonic stem cell
28	chr1:185100400-185106400	Strong transcription	Cortex derived primary cultured neurospheres	brain
29	chr1:185100800-185105800	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
30	chr1:185100800-185111200	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
31	chr1:185101000-185105400	Strong transcription	Skeletal Muscle Male	skeletal muscle
32	chr1:185101000-185105600	Strong transcription	Thymus	Thymus
33	chr1:185101000-185106200	Strong transcription	Duodenum Mucosa	Duodenum
34	chr1:185101000-185121000	Strong transcription	Primary monocytes fromperipheralblood	blood
35	chr1:185101200-185106600	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
36	chr1:185101200-185107000	Strong transcription	Fetal Muscle Trunk	muscle
37	chr1:185101400-185107000	Strong transcription	iPS-18 Cell Line	embryonic stem cell
38	chr1:185101400-185108600	Strong transcription	Primary T cells fromperipheralblood	blood
39	chr1:185101600-185105200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
40	chr1:185101600-185105200	Weak transcription	Psoas Muscle	Psoas
41	chr1:185101600-185105800	Strong transcription	Fetal Thymus	thymus
42	chr1:185101600-185125200	Weak transcription	Esophagus	oesophagus
43	chr1:185101800-185120200	Strong transcription	Adipose Nuclei	Adipose
44	chr1:185101800-185120800	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
45	chr1:185102000-185120800	Strong transcription	Placenta	Placenta
46	chr1:185102200-185105200	Weak transcription	Rectal Mucosa Donor 29	rectum
47	chr1:185102200-185109200	Strong transcription	HUES64 Cell Line	embryonic stem cell
48	chr1:185102400-185108800	Strong transcription	Left Ventricle	heart
49	chr1:185102400-185110600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
50	chr1:185102400-185113400	Weak transcription	HUVEC	blood vessel

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