Variant report

Variant	nsv875621
Chromosome Location	chr2:191117120-191177131
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:475)
CpG islands
(count:61)
Chromatin interactive
region (count:34)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:475 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:191142015-191142597	K562	blood:	n/a	n/a
2	ARID3A	chr2:191136383-191137472	K562	blood:	n/a	n/a
3	ARID3A	chr2:191134968-191135472	HepG2	liver:	n/a	n/a
4	ARID3A	chr2:191131139-191131320	HepG2	liver:	n/a	n/a
5	ARID3A	chr2:191132127-191132228	K562	blood:	n/a	n/a
6	ATF1	chr2:191168425-191168730	K562	blood:	n/a	n/a
7	ATF3	chr2:191132046-191132330	K562	blood:	n/a	n/a
8	ATF3	chr2:191134901-191135405	A549	lung:	n/a	n/a
9	BATF	chr2:191169145-191169422	GM12878	blood:	n/a	n/a
10	BCL3	chr2:191134947-191135458	A549	lung:	n/a	n/a
11	BCL3	chr2:191134952-191135398	A549	lung:	n/a	n/a
12	BCLAF1	chr2:191136875-191137459	K562	blood:	n/a	n/a
13	BCLAF1	chr2:191136937-191137527	K562	blood:	n/a	n/a
14	BHLHE40	chr2:191135082-191135356	HepG2	liver:	n/a	n/a
15	BHLHE40	chr2:191177007-191177305	K562	blood:	n/a	n/a
16	CBX3	chr2:191131875-191132508	HCT-116	colon:	n/a	n/a
17	CBX3	chr2:191131909-191132433	HCT-116	colon:	n/a	n/a
18	CCNT2	chr2:191136454-191136983	K562	blood:	n/a	n/a
19	CCNT2	chr2:191177059-191177259	K562	blood:	n/a	chr2:191177139-191177159
20	CEBPB	chr2:191156381-191156501	K562	blood:	n/a	n/a
21	CEBPB	chr2:191136528-191136802	K562	blood:	n/a	n/a
22	CEBPB	chr2:191135012-191135394	A549	lung:	n/a	n/a
23	CEBPB	chr2:191131974-191132356	IMR90	lung:	n/a	n/a
24	CEBPB	chr2:191131935-191132391	A549	lung:	n/a	n/a
25	CEBPB	chr2:191169261-191169326	A549	lung:	n/a	n/a
26	CEBPB	chr2:191136420-191136908	K562	blood:	n/a	n/a
27	CEBPB	chr2:191142356-191142593	K562	blood:	n/a	n/a
28	CEBPB	chr2:191136516-191136914	K562	blood:	n/a	n/a
29	CEBPB	chr2:191134956-191135473	A549	lung:	n/a	n/a
30	CEBPD	chr2:191177033-191177376	K562	blood:	n/a	n/a
31	CEBPD	chr2:191136429-191137096	K562	blood:	n/a	n/a
32	CEBPD	chr2:191136412-191137042	K562	blood:	n/a	n/a
33	CREB1	chr2:191136401-191136978	K562	blood:	n/a	n/a
34	CTCF	chr2:191141809-191142567	HCT-116	colon:	n/a	chr2:191142134-191142155 chr2:191142139-191142157 chr2:191142140-191142156
35	CTCF	chr2:191141996-191142329	MCF-7	breast:	n/a	chr2:191142134-191142155 chr2:191142139-191142157 chr2:191142140-191142156
36	CTCF	chr2:191142120-191142270	GM12869	blood:	n/a	chr2:191142134-191142155 chr2:191142139-191142157 chr2:191142140-191142156
37	CTCF	chr2:191142027-191142265	Spleen_OC	spleen:	n/a	chr2:191142134-191142155 chr2:191142139-191142157 chr2:191142140-191142156
38	CTCF	chr2:191142320-191142470	GM12873	blood:	n/a	n/a
39	CTCF	chr2:191142480-191142630	HPF	lung:	n/a	n/a
40	CTCF	chr2:191142160-191142310	HFF-Myc	foreskin:	n/a	n/a
41	CTCF	chr2:191142080-191142230	HRPEpiC	eye:	n/a	chr2:191142134-191142155 chr2:191142139-191142157 chr2:191142140-191142156
42	CTCF	chr2:191142040-191142190	HPF	lung:	n/a	chr2:191142134-191142155 chr2:191142139-191142157 chr2:191142140-191142156
43	CTCF	chr2:191142052-191142187	SK-N-SH_RA	brain:	n/a	chr2:191142134-191142155 chr2:191142139-191142157 chr2:191142140-191142156
44	CTCF	chr2:191142280-191142550	AoAF	blood vessel:	n/a	n/a
45	CTCF	chr2:191142000-191142150	HAc	cerebellar:	n/a	n/a
46	CTCF	chr2:191142014-191142370	MCF-7	breast:	n/a	chr2:191142134-191142155 chr2:191142139-191142157 chr2:191142140-191142156
47	CTCF	chr2:191141980-191142130	RPTEC	kidney:	n/a	n/a
48	CTCF	chr2:191142060-191142210	WERI-Rb-1	eye:	n/a	chr2:191142134-191142155 chr2:191142139-191142157 chr2:191142140-191142156
49	CTCF	chr2:191142080-191142230	AG10803	skin:	n/a	chr2:191142134-191142155 chr2:191142139-191142157 chr2:191142140-191142156
50	CTCF	chr2:191142040-191142190	GM12865	blood:	n/a	chr2:191142134-191142155 chr2:191142139-191142157 chr2:191142140-191142156

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:191164962-191165012	GM19239	blood:	n/a
2	chr2:191164962-191165012	CMK	blood:	n/a
3	chr2:191164962-191165012	AG09319	gingival:	n/a
4	chr2:191164962-191165012	AG04450	lung:	fetal
5	chr2:191164962-191165012	NHDF-neo	bronchial:	n/a
6	chr2:191164962-191165012	SK-N-SH_RA	brain:	n/a
7	chr2:191164962-191165012	H1-hESC	embryonic stem cell:	embryo
8	chr2:191164962-191165012	HCPEpiC	choroid plexus:	n/a
9	chr2:191164962-191165012	AG10803	skin:	n/a
10	chr2:191164962-191165012	Jurkat	blood:	n/a
11	chr2:191164962-191165012	HRCEpiC	kidney:	n/a
12	chr2:191164962-191165012	HMEC	breast:	n/a
13	chr2:191164962-191165012	GM12878	blood:	n/a
14	chr2:191164962-191165012	ECC-1	luminal epithelium:	n/a
15	chr2:191164962-191165012	MCF10A-Er-Src	breast:	n/a
16	chr2:191164962-191165012	Caco-2	colon:	n/a
17	chr2:191164962-191165012	NHBE	bronchial:	n/a
18	chr2:191164962-191165012	NB4	blood:	n/a
19	chr2:191164962-191165012	SK-N-MC	brain:	n/a
20	chr2:191164962-191165012	NH-A	brain:	n/a
21	chr2:191164962-191165012	A549	lung:	n/a
22	chr2:191164962-191165012	IMR90	lung:	fetal
23	chr2:191164962-191165012	SK-N-SH	brain:	n/a
24	chr2:191164962-191165012	SKMC	muscle:	n/a
25	chr2:191164962-191165012	K562	blood:	n/a
26	chr2:191164962-191165012	HepG2	liver:	n/a
27	chr2:191164962-191165012	HPAEpiC	pulmonary alveolar:	n/a
28	chr2:191164962-191165012	Hepatocyte	liver:	n/a
29	chr2:191164962-191165012	AoSMC	blood vessel:	n/a
30	chr2:191164962-191165012	HCF	heart:	n/a
31	chr2:191164962-191165012	HIPEpiC	eye:	n/a
32	chr2:191164962-191165012	RPTEC	kidney:	n/a
33	chr2:191164962-191165012	MCF-7	breast:	n/a
34	chr2:191164962-191165012	GM12892	blood:	n/a
35	chr2:191164962-191165012	HCT-116	colon:	n/a
36	chr2:191164962-191165012	HEEpiC	esophagus:	n/a
37	chr2:191164962-191165012	HRE	kidney:	n/a
38	chr2:191164962-191165012	T-47D	breast:	n/a
39	chr2:191164962-191165012	SAEC	small airway:	n/a
40	chr2:191164962-191165012	PFSK-1	brain:	n/a
41	chr2:191164962-191165012	HAEpiC	amniotic membrane:	n/a
42	chr2:191164962-191165012	PrEC	prostate:	n/a
43	chr2:191164962-191165012	ovcar-3	ovarian:	n/a
44	chr2:191164962-191165012	HUVEC	blood vessel:	n/a
45	chr2:191164962-191165012	GM06990	blood:	n/a
46	chr2:191164962-191165012	GM12891	blood:	n/a
47	chr2:191164962-191165012	HL-60	blood:	n/a
48	chr2:191164962-191165012	HRPEpiC	eye:	n/a
49	chr2:191164962-191165012	HCM	heart:	n/a
50	chr2:191164962-191165012	PANC-1	pancreas:	n/a

(count:34 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:191170524..191172788-chr2:191180838..191183387,2	K562	blood:
2	chr2:191121741..191124203-chr2:191135219..191137552,2	K562	blood:
3	chr2:191170524..191173911-chr2:191180343..191183387,4	K562	blood:
4	chr2:191130413..191132382-chr2:191136325..191138036,2	K562	blood:
5	chr2:191155862..191157478-chr2:191161113..191163862,2	K562	blood:
6	chr2:191140158..191142645-chr2:191177150..191178829,2	K562	blood:
7	chr2:191139673..191142084-chr2:191144127..191146923,2	K562	blood:
8	chr2:191160275..191162665-chr2:191211268..191214230,2	K562	blood:
9	chr2:191155862..191157478-chr2:191161113..191163862,2	K562	blood:
10	chr2:191120109..191122683-chr2:191126215..191128270,2	K562	blood:
11	chr2:191176802..191182284-chr2:191182793..191185787,7	MCF-7	breast:
12	chr2:191156936..191159599-chr2:191165960..191167883,2	MCF-7	breast:
13	chr2:191130413..191132382-chr2:191136325..191138036,2	K562	blood:
14	chr2:191173738..191175735-chr2:191400654..191403444,2	K562	blood:
15	chr2:191135876..191138298-chr2:191182929..191184673,2	K562	blood:
16	chr2:191146808..191148999-chr2:191158646..191161593,2	K562	blood:
17	chr2:191172155..191173728-chr2:191183578..191185110,2	MCF-7	breast:
18	chr2:191156936..191159599-chr2:191165960..191167883,2	MCF-7	breast:
19	chr2:190986611..190987448-chr2:191141496..191142224,3	MCF-7	breast:
20	chr2:191164735..191167364-chr2:191183015..191185017,2	MCF-7	breast:
21	chr2:190953738..190954653-chr2:191141632..191142493,2	MCF-7	breast:
22	chr2:191135269..191137265-chr2:191140643..191144192,4	K562	blood:
23	chr2:191067344..191068056-chr2:191141661..191142510,2	MCF-7	breast:
24	chr2:191121741..191124203-chr2:191135219..191137552,2	K562	blood:
25	chr2:191120109..191122683-chr2:191126215..191128270,2	K562	blood:
26	chr2:191135877..191138606-chr2:191182929..191184673,3	K562	blood:
27	chr2:191130994..191133022-chr2:191136196..191138667,2	K562	blood:
28	chr2:191146808..191148999-chr2:191158646..191161593,2	K562	blood:
29	chr2:191047911..191048684-chr2:191141877..191142603,2	MCF-7	breast:
30	chr2:191166103..191167855-chr2:191169721..191172192,2	K562	blood:
31	chr2:191135269..191137265-chr2:191140643..191144192,4	K562	blood:
32	chr2:191130994..191133022-chr2:191136196..191138667,2	K562	blood:
33	chr2:191166103..191167855-chr2:191169721..191172192,2	K562	blood:
34	chr2:191094730..191097098-chr2:191136539..191139119,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C2orf88-3	chr2:191146325-191146379	l_2008_chr2:191107785-191141547_brain
2	lnc-C2orf88-3	chr2:191141042-191141599	l_2008_chr2:191107785-191141547_brain

No data

Variant related genes	Relation type
HIBCH	TF binding region
HIBCH	CpG island
ENSG00000187699	chromatin interactions
ENSG00000198130	chromatin interactions

Extended variants
information (count: 2396 )
Associated
traits (count: 48 )

Variant overlapped rSNPs/rCNVs (count:2396 , 50 per page) page: 1 2 3 4 5 6 7 ... 48

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs291401	chr2:191117120-191117121	Weak transcription Strong transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs573689761	chr2:191117163-191117164	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs291402	chr2:191117206-191117207	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
4	rs544817629	chr2:191117208-191117209	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs75477856	chr2:191117293-191117294	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs182935941	chr2:191117294-191117295	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs542916026	chr2:191117309-191117310	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs562954930	chr2:191117311-191117312	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs560365695	chr2:191117334-191117335	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs533280219	chr2:191117340-191117341	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs576793405	chr2:191117360-191117361	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs545108933	chr2:191117401-191117402	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs150849416	chr2:191117403-191117404	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs184920172	chr2:191117425-191117426	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs528315188	chr2:191117427-191117428	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs372017916	chr2:191117433-191117434	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs561476548	chr2:191117440-191117441	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs190906467	chr2:191117467-191117468	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs549986054	chr2:191117471-191117472	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs115911068	chr2:191117479-191117480	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs532319515	chr2:191117493-191117494	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs150948695	chr2:191117504-191117505	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs183228590	chr2:191117524-191117525	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs546841960	chr2:191117527-191117528	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs536294809	chr2:191117606-191117607	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs139474808	chr2:191117621-191117622	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs187516723	chr2:191117638-191117639	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs291403	chr2:191117640-191117641	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
29	rs532682294	chr2:191117641-191117642	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs550795755	chr2:191117642-191117643	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs558592311	chr2:191117643-191117644	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs139264050	chr2:191117644-191117645	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs291404	chr2:191117653-191117654	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
34	rs527516144	chr2:191117678-191117679	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs545546882	chr2:191117692-191117693	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs183110437	chr2:191117701-191117702	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs554082076	chr2:191117705-191117706	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs572400230	chr2:191117707-191117708	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs145636046	chr2:191117772-191117773	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs543702662	chr2:191117818-191117819	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs374516154	chr2:191117830-191117831	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs188338951	chr2:191117839-191117840	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs113383585	chr2:191117840-191117841	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs369435680	chr2:191117841-191117842	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs543576121	chr2:191117852-191117853	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs565336016	chr2:191117859-191117860	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs532357190	chr2:191117867-191117868	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs547605094	chr2:191117877-191117878	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs531283724	chr2:191117954-191117955	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs145506735	chr2:191117969-191117970	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:48)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	21979893	CNVD
Ependymoma	16718352	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Melanoma	18172304	CNVD
Cancer	16751803	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Testicular germ cell tumor	18059402	CNVD
Breast cancer	16272173	CNVD
Ewing''s sarcoma	17952124	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Autism	16446308	CNVD
Autism	19401682	CNVD
Colorectal cancer	16272173	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Lung cancer	18438408	CNVD
Glioblastoma	21080181	CNVD
Prostate cancer	18632612	CNVD
Acute myeloid leukemia	20729466	CNVD
small cell lung cancer	20016488	CNVD
Facial dysmorphism	20548289	CNVD
Mental retardation	20548289	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Hirschsprung''s Disease	21712996	CNVD
Cancer	21183584	CNVD
Ovarian cancer	21720365	CNVD
Immune disease	21076436	CNVD
Immune disease	21042300	CNVD
Colorectal cancer	16912164	CNVD
Breast cancer	21364760	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:1442 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:191056800-191124600	Weak transcription	Pancreatic Islets	Pancreatic Islet
2	chr2:191056800-191131800	Weak transcription	NHEK	skin
3	chr2:191060800-191180000	Weak transcription	Small Intestine	intestine
4	chr2:191089000-191128800	Weak transcription	Gastric	stomach
5	chr2:191096800-191117400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
6	chr2:191099400-191131800	Weak transcription	HMEC	breast
7	chr2:191100000-191122400	Weak transcription	Colonic Mucosa	Colon
8	chr2:191100000-191150400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
9	chr2:191100400-191128000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
10	chr2:191104400-191151000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
11	chr2:191105000-191180000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
12	chr2:191106000-191117200	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
13	chr2:191106200-191117200	Strong transcription	Liver	Liver
14	chr2:191106200-191117400	Strong transcription	Adipose Nuclei	Adipose
15	chr2:191106200-191132200	Weak transcription	Hela-S3	cervix
16	chr2:191106600-191117200	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
17	chr2:191106600-191131800	Weak transcription	NHLF	lung
18	chr2:191106800-191117200	Strong transcription	Breast Myoepithelial Primary Cells	Breast
19	chr2:191106800-191118000	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
20	chr2:191107000-191122400	Strong transcription	Primary B cells from cord blood	blood
21	chr2:191107400-191122800	Weak transcription	HSMMtube	muscle
22	chr2:191107400-191150600	Weak transcription	Rectal Smooth Muscle	rectum
23	chr2:191107600-191117200	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
24	chr2:191107800-191125600	Weak transcription	Placenta Amnion	Placenta Amnion
25	chr2:191108000-191129400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
26	chr2:191108200-191122400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
27	chr2:191108200-191129200	Weak transcription	Spleen	Spleen
28	chr2:191108200-191135400	Weak transcription	Right Ventricle	heart
29	chr2:191108200-191180000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
30	chr2:191108800-191118200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
31	chr2:191108800-191124600	Weak transcription	H9 Cell Line	embryonic stem cell
32	chr2:191109000-191122400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
33	chr2:191109200-191119800	Weak transcription	Left Ventricle	heart
34	chr2:191109600-191120000	Weak transcription	Colon Smooth Muscle	Colon
35	chr2:191109600-191120400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
36	chr2:191109600-191122200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
37	chr2:191109600-191122400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
38	chr2:191109600-191122400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
39	chr2:191109600-191122400	Weak transcription	Fetal Brain Male	brain
40	chr2:191109600-191122400	Weak transcription	Lung	lung
41	chr2:191109600-191122400	Weak transcription	Thymus	Thymus
42	chr2:191109600-191123200	Weak transcription	Muscle Satellite Cultured Cells	--
43	chr2:191109600-191124000	Weak transcription	Esophagus	oesophagus
44	chr2:191109600-191126600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
45	chr2:191109600-191128000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
46	chr2:191109600-191135800	Weak transcription	Fetal Brain Female	brain
47	chr2:191109800-191118200	Weak transcription	NH-A	brain
48	chr2:191109800-191121600	Weak transcription	A549	lung
49	chr2:191109800-191122400	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
50	chr2:191109800-191122400	Weak transcription	Placenta	Placenta

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