Variant report

Variant	nsv999736
Chromosome Location	chr2:98706669-98811075
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:668)
CpG islands
(count:732)
Chromatin interactive
region (count:31)
LncRNA
region (count:8)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:668 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr2:98716824-98717232	K562	blood:	n/a	n/a
2	ATF1	chr2:98707651-98707822	K562	blood:	n/a	n/a
3	ATF1	chr2:98751199-98751430	K562	blood:	n/a	n/a
4	ATF2	chr2:98750612-98751042	GM12878	blood:	n/a	n/a
5	ATF2	chr2:98750595-98751083	GM12878	blood:	n/a	n/a
6	ATF3	chr2:98751111-98751462	K562	blood:	n/a	n/a
7	BACH1	chr2:98793964-98794164	H1-hESC	embryonic stem cell:	n/a	n/a
8	BCL11A	chr2:98750707-98751062	GM12878	blood:	n/a	n/a
9	BCLAF1	chr2:98750539-98751000	GM12878	blood:	n/a	n/a
10	BHLHE40	chr2:98765949-98765950	K562	blood:	n/a	n/a
11	BHLHE40	chr2:98750670-98750926	GM12878	blood:	n/a	n/a
12	BRCA1	chr2:98720913-98720924	HepG2	liver:	n/a	n/a
13	BRCA1	chr2:98722843-98722939	Hela-S3	cervix:	n/a	n/a
14	BRCA1	chr2:98732644-98732672	HepG2	liver:	n/a	n/a
15	CEBPB	chr2:98787614-98787707	Hela-S3	cervix:	n/a	n/a
16	CEBPB	chr2:98785690-98785899	IMR90	lung:	n/a	n/a
17	CEBPB	chr2:98747407-98747485	K562	blood:	n/a	chr2:98747416-98747427
18	CEBPB	chr2:98809265-98809585	HepG2	liver:	n/a	chr2:98809401-98809412
19	CEBPB	chr2:98806677-98806963	A549	lung:	n/a	n/a
20	CEBPB	chr2:98747289-98747555	A549	lung:	n/a	chr2:98747416-98747427
21	CEBPB	chr2:98785677-98785917	HepG2	liver:	n/a	n/a
22	CEBPB	chr2:98765693-98766173	HepG2	liver:	n/a	n/a
23	CEBPB	chr2:98805344-98805518	K562	blood:	n/a	chr2:98805433-98805444
24	CEBPB	chr2:98745813-98746013	H1-hESC	embryonic stem cell:	n/a	n/a
25	CEBPB	chr2:98805164-98805675	MCF-7	breast:	n/a	chr2:98805433-98805444
26	CEBPB	chr2:98805261-98805649	ECC-1	luminal epithelium:	n/a	chr2:98805433-98805444
27	CEBPB	chr2:98809227-98809538	H1-hESC	embryonic stem cell:	n/a	chr2:98809401-98809412
28	CEBPB	chr2:98806657-98806993	HepG2	liver:	n/a	n/a
29	CEBPB	chr2:98805285-98805622	ECC-1	luminal epithelium:	n/a	chr2:98805433-98805444
30	CEBPB	chr2:98805147-98805703	MCF-7	breast:	n/a	chr2:98805433-98805444
31	CEBPB	chr2:98805296-98805562	H1-hESC	embryonic stem cell:	n/a	chr2:98805433-98805444
32	CEBPB	chr2:98805296-98805582	HepG2	liver:	n/a	chr2:98805433-98805444
33	CEBPB	chr2:98765828-98766099	K562	blood:	n/a	n/a
34	CEBPB	chr2:98747262-98747586	HepG2	liver:	n/a	chr2:98747416-98747427
35	CEBPB	chr2:98805273-98805558	Hela-S3	cervix:	n/a	chr2:98805433-98805444
36	CEBPB	chr2:98747247-98747562	IMR90	lung:	n/a	chr2:98747416-98747427
37	CEBPD	chr2:98746665-98746998	K562	blood:	n/a	n/a
38	CHD2	chr2:98750687-98751228	GM12878	blood:	n/a	n/a
39	CREB1	chr2:98750595-98751157	GM12878	blood:	n/a	n/a
40	CREB1	chr2:98750605-98751143	GM12878	blood:	n/a	n/a
41	CTCF	chr2:98805191-98805294	Medullo	brain:	n/a	chr2:98805226-98805247
42	CTCF	chr2:98716738-98716827	NHEK	skin:	n/a	n/a
43	CTCF	chr2:98774070-98774337	H1-hESC	embryonic stem cell:	n/a	n/a
44	CTCF	chr2:98774128-98774297	GM19239	blood:	n/a	n/a
45	CTCF	chr2:98792420-98792570	GM12874	blood:	n/a	n/a
46	CTCF	chr2:98792404-98792594	Spleen_OC	spleen:	n/a	chr2:98792419-98792427
47	CTCF	chr2:98805200-98805350	SAEC	small airway:	n/a	chr2:98805226-98805247
48	CTCF	chr2:98792480-98792630	HVMF	connective:	n/a	n/a
49	CTCF	chr2:98774143-98774255	GM13977	blood:	n/a	n/a
50	CTCF	chr2:98805183-98805334	MCF-7	breast:	n/a	chr2:98805226-98805247

(count:732 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:98809261-98809311	SKMC	muscle:	n/a
2	chr2:98755852-98755902	AG04449	skin:	fetal
3	chr2:98802898-98802948	PrEC	prostate:	n/a
4	chr2:98756447-98756497	AG09309	skin:	n/a
5	chr2:98808005-98808055	HMEC	breast:	n/a
6	chr2:98808005-98808055	SK-N-SH_RA	brain:	n/a
7	chr2:98793396-98793446	AoSMC	blood vessel:	n/a
8	chr2:98707797-98707847	H1-hESC	embryonic stem cell:	embryo
9	chr2:98808005-98808055	NHDF-neo	bronchial:	n/a
10	chr2:98794267-98794317	HNPCEpiC	eye:	n/a
11	chr2:98802898-98802948	Caco-2	colon:	n/a
12	chr2:98794267-98794317	LNCaP	prostate:	n/a
13	chr2:98803109-98803159	GM12878	blood:	n/a
14	chr2:98809261-98809311	HEEpiC	esophagus:	n/a
15	chr2:98809287-98809337	RPTEC	kidney:	n/a
16	chr2:98793396-98793446	SK-N-SH	brain:	n/a
17	chr2:98756447-98756497	HPAEpiC	pulmonary alveolar:	n/a
18	chr2:98802868-98802918	SKMC	muscle:	n/a
19	chr2:98794267-98794317	H1-hESC	embryonic stem cell:	embryo
20	chr2:98707797-98707847	BJ	skin:	n/a
21	chr2:98802898-98802948	HNPCEpiC	eye:	n/a
22	chr2:98793396-98793446	HCPEpiC	choroid plexus:	n/a
23	chr2:98808235-98808285	HL-60	blood:	n/a
24	chr2:98809287-98809337	NHBE	bronchial:	n/a
25	chr2:98707797-98707847	MCF-7	breast:	n/a
26	chr2:98808235-98808285	Caco-2	colon:	n/a
27	chr2:98755852-98755902	MCF-7	breast:	n/a
28	chr2:98707797-98707847	HAEpiC	amniotic membrane:	n/a
29	chr2:98802898-98802948	HCT-116	colon:	n/a
30	chr2:98707797-98707847	HCF	heart:	n/a
31	chr2:98808005-98808055	Jurkat	blood:	n/a
32	chr2:98756447-98756497	SKMC	muscle:	n/a
33	chr2:98803109-98803159	IMR90	lung:	fetal
34	chr2:98803109-98803159	ProgFib	skin:	n/a
35	chr2:98756447-98756497	NT2-D1	testis:	n/a
36	chr2:98802898-98802948	HPAEpiC	pulmonary alveolar:	n/a
37	chr2:98802898-98802948	SK-N-SH	brain:	n/a
38	chr2:98755852-98755902	U87	brain:	n/a
39	chr2:98802898-98802948	HEK293	kidney:	embryo
40	chr2:98808235-98808285	GM12892	blood:	n/a
41	chr2:98809287-98809337	HCM	heart:	n/a
42	chr2:98802868-98802918	Jurkat	blood:	n/a
43	chr2:98802898-98802948	NH-A	brain:	n/a
44	chr2:98809287-98809337	HepG2	liver:	n/a
45	chr2:98756447-98756497	IMR90	lung:	fetal
46	chr2:98809287-98809337	LNCaP	prostate:	n/a
47	chr2:98755852-98755902	HRCEpiC	kidney:	n/a
48	chr2:98808235-98808285	K562	blood:	n/a
49	chr2:98707797-98707847	Caco-2	colon:	n/a
50	chr2:98793396-98793446	AG04450	lung:	fetal

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

No.	Distal block	Cell Line	Cell type
1	chr2:98758686..98760901-chr2:98772249..98774966,2	K562	blood:
2	chr2:98774522..98776569-chr2:98782191..98784432,2	K562	blood:
3	chr2:98705628..98707141-chr2:98772756..98775686,2	MCF-7	breast:
4	chr2:98758686..98760901-chr2:98772249..98774966,2	K562	blood:
5	chr2:98732440..98734489-chr2:98736889..98739713,2	K562	blood:
6	chr2:98774522..98776569-chr2:98782191..98784432,2	K562	blood:
7	chr2:98790192..98791719-chr2:98794432..98797427,2	K562	blood:
8	chr2:98611064..98613202-chr2:98773939..98776742,2	MCF-7	breast:
9	chr2:98790192..98791719-chr2:98794432..98797427,2	K562	blood:
10	chr2:98742448..98743166-chr2:140398071..140398801,2	MCF-7	breast:
11	chr2:98611501..98613824-chr2:98798072..98800088,2	MCF-7	breast:
12	chr2:98773639..98775254-chr2:98778952..98780537,2	K562	blood:
13	chr2:98600951..98603752-chr2:98713774..98716598,2	K562	blood:
14	chr2:98773639..98775254-chr2:98778952..98780537,2	K562	blood:
15	chr2:98610743..98612687-chr2:98718237..98721068,2	MCF-7	breast:
16	chr2:98766384..98769751-chr2:98776231..98780220,5	K562	blood:
17	chr2:98726208..98727848-chr2:98729692..98732563,2	K562	blood:
18	chr2:98766384..98769751-chr2:98776231..98780220,5	K562	blood:
19	chr2:98739471..98741169-chr2:98745863..98748204,2	MCF-7	breast:
20	chr2:98732440..98734489-chr2:98736889..98739713,2	K562	blood:
21	chr2:98422884..98423763-chr2:98773660..98774512,4	MCF-7	breast:
22	chr2:98726208..98727848-chr2:98729692..98732563,2	K562	blood:
23	chr2:98766384..98768153-chr2:98776231..98777799,2	K562	blood:
24	chr2:98316436..98317291-chr2:98804719..98805446,2	MCF-7	breast:
25	chr2:98702427..98705157-chr2:98705401..98707639,3	MCF-7	breast:
26	chr2:98766384..98768153-chr2:98776231..98777799,2	K562	blood:
27	chr2:98739471..98741169-chr2:98745863..98748204,2	MCF-7	breast:
28	chr2:98423370..98423923-chr2:98792023..98792988,2	K562	blood:
29	chr2:98748644..98750375-chr2:98752119..98754106,2	MCF-7	breast:
30	chr2:98705628..98707141-chr2:98772756..98775686,2	MCF-7	breast:
31	chr2:98748644..98750375-chr2:98752119..98754106,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TMEM131-3	chr2:98751856-98751941	NONHSAT072694
2	lnc-CNGA3-3	chr2:98709524-98709751	NONHSAT072691
3	lnc-TMEM131-3	chr2:98754514-98754975	NONHSAT072694
4	lnc-CNGA3-3	chr2:98732115-98732209	NONHSAT072691
5	lnc-TMEM131-3	chr2:98744833-98745473	NONHSAT072693
6	lnc-TMEM131-3	chr2:98751506-98751681	NONHSAT072693
7	lnc-CNGA3-3	chr2:98750287-98750360	NONHSAT072691
8	lnc-TMEM131-3	chr2:98751797-98751905	NONHSAT072693

No data

Variant related genes	Relation type
VWA3B	TF binding region
VWA3B	CpG island
ENSG00000075568	chromatin interactions
ENSG00000168658	chromatin interactions

Extended variants
information (count: 3701 )
Associated
traits (count: 54 )

Variant overlapped rSNPs/rCNVs (count:3701 , 50 per page) page: 1 2 3 4 5 6 7 ... 75

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs138370942	chr2:98706676-98706677	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs549186516	chr2:98706687-98706688	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs36109664	chr2:98706693-98706694	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs565872816	chr2:98706708-98706709	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs543728859	chr2:98706731-98706732	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs111678041	chr2:98706867-98706868	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs551707073	chr2:98706901-98706902	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs185380929	chr2:98706902-98706903	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs573898058	chr2:98706904-98706905	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs369438280	chr2:98706975-98706976	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs537059529	chr2:98706984-98706985	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs148830996	chr2:98707019-98707020	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs13427118	chr2:98707052-98707053	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs189093967	chr2:98707070-98707071	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs143600289	chr2:98707085-98707086	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs573110735	chr2:98707101-98707102	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs559222033	chr2:98707109-98707110	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs142626921	chr2:98707137-98707138	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs545150655	chr2:98707162-98707163	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs74423367	chr2:98707218-98707219	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs79067532	chr2:98707220-98707221	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs148070864	chr2:98707238-98707239	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs533029331	chr2:98707283-98707284	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs370061888	chr2:98707300-98707301	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs544625931	chr2:98707354-98707355	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs544704866	chr2:98707365-98707366	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs77029584	chr2:98707386-98707387	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs78123215	chr2:98707388-98707389	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs143584188	chr2:98707429-98707430	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs540382912	chr2:98707443-98707444	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs560526716	chr2:98707451-98707452	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs528319460	chr2:98707460-98707461	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs551568693	chr2:98707472-98707473	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs147193425	chr2:98707487-98707488	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs374567685	chr2:98707496-98707497	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs192043732	chr2:98707507-98707508	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs139112147	chr2:98707547-98707548	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs560015242	chr2:98707557-98707558	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs60888966	chr2:98707583-98707584	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs143093897	chr2:98707587-98707588	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs566202220	chr2:98707628-98707629	Weak transcription Active TSS Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs538860524	chr2:98707635-98707636	Weak transcription Active TSS Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs370818451	chr2:98707653-98707654	Weak transcription Active TSS Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs563292645	chr2:98707724-98707725	Weak transcription Active TSS Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs13012128	chr2:98707746-98707747	Weak transcription Active TSS Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs12996060	chr2:98707767-98707768	Weak transcription Active TSS Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs376190409	chr2:98707768-98707769	Weak transcription Active TSS Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs13012145	chr2:98707773-98707774	Weak transcription Active TSS Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs530481331	chr2:98707776-98707777	Weak transcription Active TSS Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs572006470	chr2:98707798-98707799	Weak transcription Active TSS Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:54)

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
Medulloblastoma	20607354	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
Breast cancer	21509527	CNVD
small cell lung cancer	20016488	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Myelofibrosis	22110671	CNVD
Intellectual disability	22045946	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
Glioblastoma multiforme	21138945	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD

Chromatin state (count:893 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:98704200-98707200	Weak transcription	Gastric	stomach
2	chr2:98704200-98709800	Enhancers	Primary monocytes fromperipheralblood	blood
3	chr2:98704400-98709000	Enhancers	Primary B cells from cord blood	blood
4	chr2:98704600-98707400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
5	chr2:98704800-98707400	Weak transcription	Primary hematopoietic stem cells	blood
6	chr2:98705200-98708200	Enhancers	Primary neutrophils fromperipheralblood	blood
7	chr2:98705400-98707800	Enhancers	Breast Myoepithelial Primary Cells	Breast
8	chr2:98705600-98707000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
9	chr2:98705600-98708000	Weak transcription	Adipose Nuclei	Adipose
10	chr2:98706000-98707800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
11	chr2:98706200-98708800	Enhancers	Primary B cells from peripheral blood	blood
12	chr2:98706400-98707000	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
13	chr2:98706600-98708800	Enhancers	Primary hematopoietic stem cells short term culture	blood
14	chr2:98707000-98707400	Enhancers	Monocytes-CD14+_RO01746	blood
15	chr2:98707000-98707600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
16	chr2:98707200-98708000	Enhancers	Gastric	stomach
17	chr2:98707400-98707800	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
18	chr2:98707400-98708800	Enhancers	Primary hematopoietic stem cells	blood
19	chr2:98707400-98708800	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
20	chr2:98707600-98707800	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
21	chr2:98707600-98707800	Enhancers	Fetal Muscle Leg	muscle
22	chr2:98707800-98708200	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
23	chr2:98707800-98708600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
24	chr2:98707800-98708800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
25	chr2:98707800-98708800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
26	chr2:98708200-98708400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
27	chr2:98708200-98708600	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
28	chr2:98708200-98708600	Enhancers	Fetal Muscle Leg	muscle
29	chr2:98708400-98708600	Enhancers	Adipose Nuclei	Adipose
30	chr2:98708400-98710800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
31	chr2:98708600-98709800	Enhancers	Primary neutrophils fromperipheralblood	blood
32	chr2:98708600-98710200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
33	chr2:98708800-98709800	Enhancers	Monocytes-CD14+_RO01746	blood
34	chr2:98709400-98710000	Enhancers	Fetal Thymus	thymus
35	chr2:98710200-98710400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
36	chr2:98710800-98712400	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
37	chr2:98715600-98715800	Enhancers	Primary monocytes fromperipheralblood	blood
38	chr2:98715600-98717000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
39	chr2:98715800-98716600	Enhancers	Monocytes-CD14+_RO01746	blood
40	chr2:98716400-98716600	Enhancers	Primary monocytes fromperipheralblood	blood
41	chr2:98716600-98717000	Enhancers	Fetal Heart	heart
42	chr2:98716600-98717200	Enhancers	Gastric	stomach
43	chr2:98716600-98717200	Enhancers	Left Ventricle	heart
44	chr2:98716600-98717200	Enhancers	Right Ventricle	heart
45	chr2:98716600-98717400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
46	chr2:98716800-98717200	Enhancers	Skeletal Muscle Female	skeletal muscle
47	chr2:98716800-98717400	Enhancers	Pancreas	Pancrea
48	chr2:98716800-98717400	Enhancers	Skeletal Muscle Male	skeletal muscle
49	chr2:98717200-98720800	Weak transcription	Gastric	stomach
50	chr2:98719000-98720800	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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