Variant report

Variant	nsv582697
Chromosome Location	chr2:111386233-111451816
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1216)
CpG islands
(count:1466)
Chromatin interactive
region (count:41)
LncRNA
region (count:8)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1216 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:111435595-111436162	K562	blood:	n/a	n/a
2	ARID3A	chr2:111398827-111398870	K562	blood:	n/a	n/a
3	ARID3A	chr2:111449523-111449771	K562	blood:	n/a	n/a
4	ARID3A	chr2:111436844-111437360	K562	blood:	n/a	n/a
5	ARID3A	chr2:111399730-111399777	K562	blood:	n/a	n/a
6	ARID3A	chr2:111435637-111436086	HepG2	liver:	n/a	n/a
7	ARID3A	chr2:111439309-111439638	K562	blood:	n/a	n/a
8	ATF2	chr2:111432549-111433311	GM12878	blood:	n/a	n/a
9	ATF2	chr2:111432529-111433344	GM12878	blood:	n/a	n/a
10	ATF2	chr2:111446053-111446757	H1-hESC	embryonic stem cell:	n/a	n/a
11	ATF2	chr2:111445053-111445743	H1-hESC	embryonic stem cell:	n/a	n/a
12	ATF2	chr2:111435601-111436191	GM12878	blood:	n/a	n/a
13	ATF2	chr2:111446020-111446786	H1-hESC	embryonic stem cell:	n/a	n/a
14	BACH1	chr2:111445373-111445724	H1-hESC	embryonic stem cell:	n/a	n/a
15	BACH1	chr2:111435648-111436284	H1-hESC	embryonic stem cell:	n/a	n/a
16	BACH1	chr2:111436880-111437064	H1-hESC	embryonic stem cell:	n/a	n/a
17	BACH1	chr2:111446533-111446748	K562	blood:	n/a	n/a
18	BACH1	chr2:111436617-111437068	K562	blood:	n/a	n/a
19	BACH1	chr2:111446125-111446893	H1-hESC	embryonic stem cell:	n/a	n/a
20	BACH1	chr2:111435876-111436193	K562	blood:	n/a	n/a
21	BATF	chr2:111428447-111428749	GM12878	blood:	n/a	n/a
22	BATF	chr2:111432845-111433121	GM12878	blood:	n/a	n/a
23	BCL11A	chr2:111445375-111445632	H1-hESC	embryonic stem cell:	n/a	n/a
24	BCL11A	chr2:111446354-111446724	H1-hESC	embryonic stem cell:	n/a	n/a
25	BCL11A	chr2:111446360-111446648	H1-hESC	embryonic stem cell:	n/a	n/a
26	BCL11A	chr2:111432811-111433138	GM12878	blood:	n/a	n/a
27	BCL11A	chr2:111432864-111433140	GM12878	blood:	n/a	n/a
28	BCL11A	chr2:111445368-111445654	H1-hESC	embryonic stem cell:	n/a	n/a
29	BCL3	chr2:111428458-111428841	GM12878	blood:	n/a	chr2:111428519-111428528 chr2:111428619-111428628
30	BCLAF1	chr2:111432538-111433169	GM12878	blood:	n/a	n/a
31	BCLAF1	chr2:111435670-111436542	GM12878	blood:	n/a	n/a
32	BCLAF1	chr2:111432762-111433388	GM12878	blood:	n/a	n/a
33	BCLAF1	chr2:111433232-111433528	GM12878	blood:	n/a	n/a
34	BHLHE40	chr2:111432375-111433239	GM12878	blood:	n/a	n/a
35	BHLHE40	chr2:111449506-111449706	K562	blood:	n/a	n/a
36	BHLHE40	chr2:111432660-111433136	K562	blood:	n/a	n/a
37	BHLHE40	chr2:111435601-111437823	K562	blood:	n/a	n/a
38	BHLHE40	chr2:111435201-111436778	GM12878	blood:	n/a	n/a
39	BHLHE40	chr2:111449120-111449246	K562	blood:	n/a	n/a
40	BHLHE40	chr2:111415216-111415736	GM12878	blood:	n/a	n/a
41	BRCA1	chr2:111435695-111436084	HepG2	liver:	n/a	n/a
42	BRCA1	chr2:111443644-111443658	GM12878	blood:	n/a	n/a
43	BRCA1	chr2:111435536-111435923	Hela-S3	cervix:	n/a	n/a
44	BRCA1	chr2:111436059-111436449	GM12878	blood:	n/a	n/a
45	BRCA1	chr2:111435667-111435904	H1-hESC	embryonic stem cell:	n/a	n/a
46	CBX3	chr2:111449098-111449940	K562	blood:	n/a	n/a
47	CBX3	chr2:111444910-111445253	K562	blood:	n/a	n/a
48	CBX3	chr2:111435277-111436075	K562	blood:	n/a	n/a
49	CCNT2	chr2:111434970-111436202	K562	blood:	n/a	chr2:111435521-111435530 chr2:111435503-111435512
50	CCNT2	chr2:111405920-111406156	K562	blood:	n/a	n/a

(count:1466 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:111436307-111436357	HCT-116	colon:	n/a
2	chr2:111435583-111435633	ovcar-3	ovarian:	n/a
3	chr2:111436307-111436357	HCT-116	colon:	n/a
4	chr2:111435583-111435633	ovcar-3	ovarian:	n/a
5	chr2:111436559-111436609	HMEC	breast:	n/a
6	chr2:111436326-111436376	HCPEpiC	choroid plexus:	n/a
7	chr2:111437634-111437684	AG04449	skin:	fetal
8	chr2:111435449-111435499	T-47D	breast:	n/a
9	chr2:111447255-111447305	HRCEpiC	kidney:	n/a
10	chr2:111444640-111444690	Hela-S3	cervix:	n/a
11	chr2:111444640-111444690	AoSMC	blood vessel:	n/a
12	chr2:111435858-111435908	HAEpiC	amniotic membrane:	n/a
13	chr2:111440239-111440289	HAEpiC	amniotic membrane:	n/a
14	chr2:111435449-111435499	NT2-D1	testis:	n/a
15	chr2:111438170-111438220	GM12891	blood:	n/a
16	chr2:111446533-111446583	HCM	heart:	n/a
17	chr2:111435817-111435867	HL-60	blood:	n/a
18	chr2:111435611-111435661	A549	lung:	n/a
19	chr2:111435943-111435993	HRPEpiC	eye:	n/a
20	chr2:111440239-111440289	AG09319	gingival:	n/a
21	chr2:111435828-111435878	Caco-2	colon:	n/a
22	chr2:111435850-111435900	NH-A	brain:	n/a
23	chr2:111436326-111436376	HRPEpiC	eye:	n/a
24	chr2:111435943-111435993	GM12891	blood:	n/a
25	chr2:111446533-111446583	HAEpiC	amniotic membrane:	n/a
26	chr2:111438170-111438220	HCM	heart:	n/a
27	chr2:111435850-111435900	HUVEC	blood vessel:	n/a
28	chr2:111442452-111442502	T-47D	breast:	n/a
29	chr2:111438170-111438220	MCF10A-Er-Src	breast:	n/a
30	chr2:111437634-111437684	HEEpiC	esophagus:	n/a
31	chr2:111436326-111436376	HIPEpiC	eye:	n/a
32	chr2:111435449-111435499	ovcar-3	ovarian:	n/a
33	chr2:111435449-111435499	HCT-116	colon:	n/a
34	chr2:111435943-111435993	Hela-S3	cervix:	n/a
35	chr2:111436428-111436478	SKMC	muscle:	n/a
36	chr2:111435611-111435661	ECC-1	luminal epithelium:	n/a
37	chr2:111435817-111435867	MCF-7	breast:	n/a
38	chr2:111435850-111435900	LNCaP	prostate:	n/a
39	chr2:111435611-111435661	Hepatocyte	liver:	n/a
40	chr2:111435850-111435900	T-47D	breast:	n/a
41	chr2:111442452-111442502	NT2-D1	testis:	n/a
42	chr2:111440239-111440289	HCM	heart:	n/a
43	chr2:111442452-111442502	HAEpiC	amniotic membrane:	n/a
44	chr2:111436428-111436478	AoSMC	blood vessel:	n/a
45	chr2:111447255-111447305	Hela-S3	cervix:	n/a
46	chr2:111435583-111435633	HRE	kidney:	n/a
47	chr2:111435943-111435993	AoSMC	blood vessel:	n/a
48	chr2:111435723-111435773	AG09309	skin:	n/a
49	chr2:111436428-111436478	GM06990	blood:	n/a
50	chr2:111442452-111442502	A549	lung:	n/a

(count:41 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:111435925..111437576-chr2:111510345..111513033,2	MCF-7	breast:
2	chr2:111410514..111412334-chr2:111420425..111422233,2	K562	blood:
3	chr2:111450177..111452870-chr2:111458026..111461829,3	K562	blood:
4	chr2:111412529..111415499-chr2:111427252..111428761,2	K562	blood:
5	chr2:111417412..111419778-chr2:111421877..111423912,2	MCF-7	breast:
6	chr2:111447915..111450882-chr2:111451091..111454468,3	K562	blood:
7	chr2:111393512..111396339-chr2:111405905..111409103,3	K562	blood:
8	chr2:111426617..111428514-chr2:111432222..111433753,2	MCF-7	breast:
9	chr2:111434545..111436988-chr2:111439574..111441655,2	MCF-7	breast:
10	chr2:111404628..111406815-chr2:111414817..111418033,3	K562	blood:
11	chr2:111410330..111414018-chr2:111416096..111419092,4	K562	blood:
12	chr2:111409847..111412405-chr2:111435701..111437237,2	K562	blood:
13	chr2:111409847..111412405-chr2:111435701..111437237,2	K562	blood:
14	chr2:111447507..111449060-chr2:111488043..111489984,2	MCF-7	breast:
15	chr2:111393886..111396195-chr2:111397054..111399333,2	K562	blood:
16	chr2:111410330..111414018-chr2:111416096..111419092,4	K562	blood:
17	chr2:111450205..111452160-chr2:111469242..111471005,2	MCF-7	breast:
18	chr2:111439653..111442427-chr2:111447618..111449255,2	MCF-7	breast:
19	chr2:111395384..111398078-chr2:111408788..111411158,2	K562	blood:
20	chr2:111422527..111426501-chr2:111427034..111430366,4	K562	blood:
21	chr2:111412036..111414353-chr2:111428995..111431302,2	K562	blood:
22	chr2:111435750..111438683-chr2:111457735..111460578,3	K562	blood:
23	chr2:111404628..111406815-chr2:111414817..111418033,3	K562	blood:
24	chr2:111434111..111436826-chr2:111878321..111880919,2	K562	blood:
25	chr2:111412036..111414353-chr2:111428995..111431302,2	K562	blood:
26	chr2:111426617..111428514-chr2:111432222..111433753,2	MCF-7	breast:
27	chr2:111447915..111450882-chr2:111451091..111454468,3	K562	blood:
28	chr2:111417412..111419778-chr2:111421877..111423912,2	MCF-7	breast:
29	chr2:111395384..111398078-chr2:111408788..111411158,2	K562	blood:
30	chr2:111412529..111415499-chr2:111427252..111428761,2	K562	blood:
31	chr2:111422527..111426501-chr2:111427034..111430366,4	K562	blood:
32	chr2:111439653..111442427-chr2:111447618..111449255,2	MCF-7	breast:
33	chr2:111449352..111451677-chr2:111460329..111462604,2	K562	blood:
34	chr2:111412529..111421605-chr2:111423929..111428761,11	K562	blood:
35	chr2:111399412..111401364-chr2:111406078..111408025,2	K562	blood:
36	chr2:111422408..111425230-chr2:111426380..111428328,2	K562	blood:
37	chr2:111393886..111396195-chr2:111397054..111399333,2	K562	blood:
38	chr2:111410514..111412334-chr2:111420425..111422233,2	K562	blood:
39	chr2:111422408..111425230-chr2:111426380..111428328,2	K562	blood:
40	chr2:111417148..111420155-chr2:111422664..111426427,4	K562	blood:
41	chr2:111434937..111436976-chr2:111438707..111440679,2	MCF-7	breast:

(count:8 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-BUB1-2	chr2:111450096-111450363	NONHSAT073422
2	lnc-ACOXL-3	chr2:111435835-111436174	NONHSAT073229
3	lnc-RGPD6-1	chr2:111408123-111408316	NONHSAT073226
4	lnc-ACOXL-3	chr2:111439990-111440038	NONHSAT073229
5	lnc-RGPD6-1	chr2:111406394-111406954	NONHSAT073226
6	lnc-ACOXL-3	chr2:111450096-111450964	NONHSAT073228
7	lnc-BUB1-2	chr2:111450756-111451158	NONHSAT073422
8	lnc-ACOXL-3	chr2:111435835-111436174	NONHSAT073228

No data

Variant related genes	Relation type
BUB1	TF binding region
ENSG00000216867	TF binding region
BUB1	CpG island
ENSG00000216867	CpG island
ENSG00000169679	chromatin interactions
ENSG00000153094	chromatin interactions

Extended variants
information (count: 2096 )
Associated
traits (count: 72 )

Variant overlapped rSNPs/rCNVs (count:2096 , 50 per page) page: 1 2 3 4 5 6 7 ... 42

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs112202418	chr2:111386233-111386234	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs542666114	chr2:111386268-111386269	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs562417126	chr2:111386278-111386279	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs531519751	chr2:111386380-111386381	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs199970169	chr2:111386421-111386422	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs564741248	chr2:111386485-111386486	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs559589490	chr2:111386536-111386537	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs547616819	chr2:111386605-111386606	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs367547292	chr2:111386639-111386640	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs528520745	chr2:111386654-111386655	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs567636763	chr2:111386744-111386745	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs536223366	chr2:111386801-111386802	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs550213951	chr2:111387004-111387005	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs570322812	chr2:111387173-111387174	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs539342744	chr2:111387260-111387261	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs559190145	chr2:111387265-111387266	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs201133485	chr2:111387311-111387312	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs533868118	chr2:111387383-111387384	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs553612626	chr2:111387609-111387610	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs79383267	chr2:111387619-111387620	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs571929378	chr2:111387674-111387675	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs55821241	chr2:111387676-111387677	Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs116647513	chr2:111387687-111387688	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs566239868	chr2:111387713-111387714	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs575889153	chr2:111387751-111387752	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs544949223	chr2:111387845-111387846	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs565082416	chr2:111387856-111387857	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs527528319	chr2:111387887-111387888	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs547849543	chr2:111387903-111387904	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs568718618	chr2:111388093-111388094	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs561189890	chr2:111388120-111388121	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs112117569	chr2:111388292-111388293	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs530220285	chr2:111388386-111388387	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs12999402	chr2:111388480-111388481	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs531193307	chr2:111388499-111388500	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs200221428	chr2:111388527-111388528	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs550152539	chr2:111388561-111388562	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs570112276	chr2:111388615-111388616	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs532843483	chr2:111388632-111388633	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs140541720	chr2:111388675-111388676	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs566239740	chr2:111388690-111388691	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs534879207	chr2:111388702-111388703	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs555162603	chr2:111388781-111388782	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs567211675	chr2:111388793-111388794	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs187593035	chr2:111388855-111388856	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs202083652	chr2:111388925-111388926	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs150048391	chr2:111388926-111388927	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs145243778	chr2:111388960-111388961	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs558607503	chr2:111388963-111388964	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs377458382	chr2:111388993-111388994	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:72)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Breast cancer	17603634	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Ependymoma	16718352	CNVD
Prostate cancer	18632612	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Autism	17483303	CNVD
Autism	22495311	CNVD
Autism	18522746	CNVD
Neurodevelopmental disorder	22521361	CNVD
Melanoma	18172304	CNVD
Cancer	16751803	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Seminomas	18059402	CNVD
Testicular germ cell tumor	18059402	CNVD
Myxofibrosarcoma	16751306	CNVD
Breast cancer	16272173	CNVD
Ovarian cancer	21781307	CNVD
Lung cancer	18438408	CNVD
Mowat-Wilson syndrome	21572526	CNVD
Disorders of sex development	21048976	CNVD
epilepsy	18472482	CNVD
Ewing''s sarcoma	17952124	CNVD
Hepatocellular carcinoma	16750200	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
lymphocytic leukemia	21291569	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Colorectal cancer	16272173	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
myoclonus epilepsy	18472482	CNVD
Benign familial neonatal-infantile seizures	18472482	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Astrocytoma	22246337	CNVD
Myelofibrosis	22110671	CNVD
Ocular motor apraxia	21572526	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Congenital abnormalities	21549014	CNVD
Developmental delay	21549014	CNVD
Idiopathic chronic pancreatitis	21549014	CNVD
Mental retardation	21549014	CNVD
Maculopathy	20981449	CNVD
Nephronophthisis	22470819	CNVD
Colorectal cancer	16912164	CNVD
Ischaemic stroke	16980335	CNVD
Acute myeloid leukemia	18000384	CNVD
Nephronophthisis	17901113	CNVD
small cell lung cancer	20016488	CNVD
Schizophrenia	23813976	CNVD
Developmental delay	21147756	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Autism	20808228	CNVD
Clear cell renal cell carcinoma	18791270	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD

Chromatin state (count:1663 , 50 per page) page: 1 2 3 4 5 6 7 ... 34

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:111377600-111392000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
2	chr2:111384200-111410200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
3	chr2:111385200-111391800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr2:111385400-111392000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
5	chr2:111385400-111396000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr2:111386200-111392000	Weak transcription	Dnd41	blood
7	chr2:111386200-111395400	Weak transcription	HMEC	breast
8	chr2:111387000-111392000	Weak transcription	A549	lung
9	chr2:111388000-111392200	Weak transcription	Fetal Thymus	thymus
10	chr2:111389000-111394400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
11	chr2:111390200-111392000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
12	chr2:111390200-111392000	Weak transcription	HUES6 Cell Line	embryonic stem cell
13	chr2:111390200-111392000	Weak transcription	HUES64 Cell Line	embryonic stem cell
14	chr2:111390200-111392000	Weak transcription	Primary neutrophils fromperipheralblood	blood
15	chr2:111390200-111392000	Weak transcription	Thymus	Thymus
16	chr2:111390200-111392000	Weak transcription	Monocytes-CD14+_RO01746	blood
17	chr2:111390400-111392000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
18	chr2:111390400-111392000	Weak transcription	Primary hematopoietic stem cells	blood
19	chr2:111390400-111392000	Weak transcription	Muscle Satellite Cultured Cells	--
20	chr2:111390400-111392000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
21	chr2:111390400-111392000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
22	chr2:111390400-111392000	Weak transcription	Fetal Stomach	stomach
23	chr2:111390400-111392000	Weak transcription	GM12878-XiMat	blood
24	chr2:111390400-111392200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
25	chr2:111390400-111392200	Weak transcription	HUES48 Cell Line	embryonic stem cell
26	chr2:111390400-111392200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
27	chr2:111390400-111392200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
28	chr2:111390400-111392200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
29	chr2:111390400-111392200	Weak transcription	HUVEC	blood vessel
30	chr2:111390600-111392200	Weak transcription	H1 Cell Line	embryonic stem cell
31	chr2:111390600-111392200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
32	chr2:111390600-111392200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
33	chr2:111390600-111392200	Weak transcription	Cortex derived primary cultured neurospheres	brain
34	chr2:111390600-111392200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
35	chr2:111390600-111392200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
36	chr2:111390600-111392200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
37	chr2:111390600-111392200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
38	chr2:111390600-111392200	Weak transcription	HepG2	liver
39	chr2:111390600-111392200	Weak transcription	NHDF-Ad	bronchial
40	chr2:111390600-111394400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
41	chr2:111390600-111394400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
42	chr2:111390600-111394400	Weak transcription	Primary monocytes fromperipheralblood	blood
43	chr2:111390600-111394400	Weak transcription	NH-A	brain
44	chr2:111390600-111394400	Weak transcription	Osteobl	bone
45	chr2:111390600-111396000	Weak transcription	Fetal Muscle Trunk	muscle
46	chr2:111390600-111396400	Weak transcription	Fetal Intestine Large	intestine
47	chr2:111390600-111397000	Weak transcription	Fetal Lung	lung
48	chr2:111390600-111397200	Weak transcription	NHEK	skin
49	chr2:111390800-111392200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
50	chr2:111390800-111394600	Weak transcription	HSMM	muscle

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links