Variant report

Variant	esv3342589
Chromosome Location	chr2:98205045-98208093
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	ARID3A	chr2:98207279-98207593	K562	blood:	n/a	n/a
2	ARID3A	chr2:98207224-98207615	HepG2	liver:	n/a	n/a
3	ATF1	chr2:98207276-98207536	K562	blood:	n/a	n/a
4	ATF3	chr2:98207210-98207581	K562	blood:	n/a	n/a
5	BATF	chr2:98207309-98207641	GM12878	blood:	n/a	n/a
6	BATF	chr2:98206887-98207071	GM12878	blood:	n/a	n/a
7	BATF	chr2:98206281-98206755	GM12878	blood:	n/a	n/a
8	BATF	chr2:98207363-98207686	GM12878	blood:	n/a	n/a
9	BCL11A	chr2:98206444-98207010	GM12878	blood:	n/a	chr2:98206849-98206862 chr2:98206762-98206775
10	BCL11A	chr2:98207352-98207590	GM12878	blood:	n/a	chr2:98207572-98207579
11	BCL11A	chr2:98205341-98205570	GM12878	blood:	n/a	n/a
12	BCLAF1	chr2:98207201-98207637	GM12878	blood:	n/a	chr2:98207572-98207579
13	BHLHE40	chr2:98206265-98206289	GM12878	blood:	n/a	n/a
14	BHLHE40	chr2:98206228-98206632	HepG2	liver:	n/a	n/a
15	BHLHE40	chr2:98207280-98207592	GM12878	blood:	n/a	n/a
16	BHLHE40	chr2:98206179-98206453	K562	blood:	n/a	n/a
17	BRCA1	chr2:98207285-98207646	Hela-S3	cervix:	n/a	n/a
18	CBX3	chr2:98207164-98207600	K562	blood:	n/a	n/a
19	CBX3	chr2:98206107-98207533	K562	blood:	n/a	n/a
20	CBX3	chr2:98206082-98206466	K562	blood:	n/a	n/a
21	CCNT2	chr2:98206271-98206359	K562	blood:	n/a	n/a
22	CEBPD	chr2:98206159-98206391	HepG2	liver:	n/a	n/a
23	CHD1	chr2:98207385-98207408	GM12878	blood:	n/a	n/a
24	CHD2	chr2:98207250-98207471	HepG2	liver:	n/a	n/a
25	CHD2	chr2:98206243-98206454	K562	blood:	n/a	n/a
26	CHD2	chr2:98206306-98206498	Hela-S3	cervix:	n/a	n/a
27	CHD2	chr2:98207321-98207531	GM12878	blood:	n/a	n/a
28	CHD2	chr2:98206316-98206476	HepG2	liver:	n/a	n/a
29	CTCF	chr2:98207227-98207595	H1-hESC	embryonic stem cell:	n/a	chr2:98207475-98207496 chr2:98207416-98207437 chr2:98207473-98207491 chr2:98207419-98207427 chr2:98207474-98207490 chr2:98207414-98207432
30	CTCF	chr2:98206689-98206995	GM13977	blood:	n/a	chr2:98206933-98206946 chr2:98206828-98206841
31	CTCF	chr2:98206681-98206919	K562	blood:	n/a	chr2:98206828-98206841
32	CTCF	chr2:98206620-98206770	HFF	foreskin:	n/a	n/a
33	CTCF	chr2:98207400-98207550	HepG2	liver:	n/a	chr2:98207475-98207496 chr2:98207416-98207437 chr2:98207473-98207491 chr2:98207419-98207427 chr2:98207474-98207490 chr2:98207414-98207432
34	CTCF	chr2:98206747-98206918	LNCaP	prostate:	n/a	chr2:98206828-98206841
35	CTCF	chr2:98206560-98206710	GM12878	blood:	n/a	n/a
36	CTCF	chr2:98207320-98207470	GM12801	blood:	n/a	chr2:98207416-98207437 chr2:98207419-98207427 chr2:98207414-98207432
37	CTCF	chr2:98207380-98207530	HPF	lung:	n/a	chr2:98207475-98207496 chr2:98207416-98207437 chr2:98207473-98207491 chr2:98207419-98207427 chr2:98207474-98207490 chr2:98207414-98207432
38	CTCF	chr2:98207380-98207530	AG04449	skin:	n/a	chr2:98207475-98207496 chr2:98207416-98207437 chr2:98207473-98207491 chr2:98207419-98207427 chr2:98207474-98207490 chr2:98207414-98207432
39	CTCF	chr2:98206683-98207112	LNCaP	prostate:	n/a	chr2:98206933-98206946 chr2:98206828-98206841
40	CTCF	chr2:98207300-98207450	BE2_C	brain:	n/a	chr2:98207416-98207437 chr2:98207419-98207427 chr2:98207414-98207432
41	CTCF	chr2:98206669-98206947	MCF-7	breast:	n/a	chr2:98206933-98206946 chr2:98206828-98206841
42	CTCF	chr2:98207380-98207530	GM12871	blood:	n/a	chr2:98207475-98207496 chr2:98207416-98207437 chr2:98207473-98207491 chr2:98207419-98207427 chr2:98207474-98207490 chr2:98207414-98207432
43	CTCF	chr2:98207320-98207470	SK-N-SH_RA	brain:	n/a	chr2:98207416-98207437 chr2:98207419-98207427 chr2:98207414-98207432
44	CTCF	chr2:98207400-98207550	GM12875	blood:	n/a	chr2:98207475-98207496 chr2:98207416-98207437 chr2:98207473-98207491 chr2:98207419-98207427 chr2:98207474-98207490 chr2:98207414-98207432
45	CTCF	chr2:98206980-98207130	WI-38	lung:	n/a	n/a
46	CTCF	chr2:98206663-98207012	GM10248	blood:	n/a	chr2:98206933-98206946 chr2:98206828-98206841
47	CTCF	chr2:98206775-98206872	HUVEC	blood vessel:	n/a	chr2:98206828-98206841
48	CTCF	chr2:98207380-98207530	HBMEC	blood vessel:	n/a	chr2:98207475-98207496 chr2:98207416-98207437 chr2:98207473-98207491 chr2:98207419-98207427 chr2:98207474-98207490 chr2:98207414-98207432
49	CTCF	chr2:98207320-98207470	GM12865	blood:	n/a	chr2:98207416-98207437 chr2:98207419-98207427 chr2:98207414-98207432
50	CTCF	chr2:98207259-98207604	HUVEC	blood vessel:	n/a	chr2:98207475-98207496 chr2:98207416-98207437 chr2:98207473-98207491 chr2:98207419-98207427 chr2:98207474-98207490 chr2:98207414-98207432

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:98206249-98206299	HRE	kidney:	n/a
2	chr2:98206249-98206299	HRE	kidney:	n/a
3	chr2:98207378-98207428	HCM	heart:	n/a
4	chr2:98207190-98207240	RPTEC	kidney:	n/a
5	chr2:98205903-98205953	GM06990	blood:	n/a
6	chr2:98206249-98206299	Caco-2	colon:	n/a
7	chr2:98207190-98207240	Jurkat	blood:	n/a
8	chr2:98207378-98207428	PFSK-1	brain:	n/a
9	chr2:98207190-98207240	ECC-1	luminal epithelium:	n/a
10	chr2:98207378-98207428	Jurkat	blood:	n/a
11	chr2:98206733-98206783	H1-hESC	embryonic stem cell:	embryo
12	chr2:98205903-98205953	NHDF-neo	bronchial:	n/a
13	chr2:98206095-98206145	CMK	blood:	n/a
14	chr2:98206702-98206752	HCPEpiC	choroid plexus:	n/a
15	chr2:98206175-98206225	K562	blood:	n/a
16	chr2:98206249-98206299	IMR90	lung:	fetal
17	chr2:98205903-98205953	ECC-1	luminal epithelium:	n/a
18	chr2:98206733-98206783	A549	lung:	n/a
19	chr2:98207190-98207240	HRPEpiC	eye:	n/a
20	chr2:98206095-98206145	HIPEpiC	eye:	n/a
21	chr2:98206249-98206299	HEK293	kidney:	embryo
22	chr2:98205903-98205953	IMR90	lung:	fetal
23	chr2:98205903-98205953	NB4	blood:	n/a
24	chr2:98205903-98205953	HL-60	blood:	n/a
25	chr2:98206702-98206752	SK-N-SH_RA	brain:	n/a
26	chr2:98206249-98206299	NHDF-neo	bronchial:	n/a
27	chr2:98206175-98206225	HMEC	breast:	n/a
28	chr2:98207378-98207428	H1-hESC	embryonic stem cell:	embryo
29	chr2:98206702-98206752	HMEC	breast:	n/a
30	chr2:98206702-98206752	H1-hESC	embryonic stem cell:	embryo
31	chr2:98206702-98206752	PrEC	prostate:	n/a
32	chr2:98205903-98205953	Hela-S3	cervix:	n/a
33	chr2:98206702-98206752	AG10803	skin:	n/a
34	chr2:98205903-98205953	SAEC	small airway:	n/a
35	chr2:98207190-98207240	U87	brain:	n/a
36	chr2:98207190-98207240	MCF10A-Er-Src	breast:	n/a
37	chr2:98207190-98207240	NB4	blood:	n/a
38	chr2:98207190-98207240	GM06990	blood:	n/a
39	chr2:98206733-98206783	HEK293	kidney:	embryo
40	chr2:98206249-98206299	HUVEC	blood vessel:	n/a
41	chr2:98206702-98206752	GM12891	blood:	n/a
42	chr2:98206733-98206783	PrEC	prostate:	n/a
43	chr2:98206095-98206145	Caco-2	colon:	n/a
44	chr2:98206175-98206225	LNCaP	prostate:	n/a
45	chr2:98206095-98206145	PFSK-1	brain:	n/a
46	chr2:98206095-98206145	Hela-S3	cervix:	n/a
47	chr2:98205903-98205953	HUVEC	blood vessel:	n/a
48	chr2:98207378-98207428	IMR90	lung:	fetal
49	chr2:98206249-98206299	ProgFib	skin:	n/a
50	chr2:98206733-98206783	CMK	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr2:98206110..98207769-chr2:98279652..98281540,2	K562	blood:
2	chr2:98205848..98207835-chr2:98279004..98283186,3	MCF-7	breast:
3	chr2:98204043..98208769-chr2:98260858..98263741,4	MCF-7	breast:
4	chr2:98207030..98207867-chr2:98316437..98317264,2	MCF-7	breast:
5	chr2:98207000..98207853-chr2:219712161..219712679,2	MCF-7	breast:
6	chr2:98207030..98207891-chr2:98316572..98317381,2	K562	blood:
7	chr2:98206925..98207973-chr2:98313358..98314529,26	K562	blood:
8	chr2:98207335..98207918-chr2:98313479..98314662,4	MCF-7	breast:
9	chr2:98206838..98208035-chr2:98280277..98281403,5	MCF-7	breast:
10	chr2:98207345..98207911-chr2:98364591..98365105,3	K562	blood:
11	chr2:98207043..98207962-chr2:98341661..98342410,2	MCF-7	breast:
12	chr2:98206697..98208046-chr2:98313463..98314373,16	MCF-7	breast:
13	chr2:98205832..98206585-chr20:2450969..2451709,2	NB4	blood:

Variant related genes	Relation type
ANKRD36B	TF binding region
ANKRD36B	CpG island
ENSG00000201806	chromatin interactions
ENSG00000135940	chromatin interactions
ENSG00000115073	chromatin interactions
ENSG00000125835	chromatin interactions
ENSG00000228486	chromatin interactions

Extended variants
information (count: 96 )
Associated
traits (count: 52 )

Variant overlapped rSNPs/rCNVs (count:96 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs201917219	chr2:98205243-98205244	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs3866780	chr2:98205416-98205417	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs1809113	chr2:98205724-98205725	Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs1814508	chr2:98205744-98205745	Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs563999457	chr2:98205799-98205800	Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs2924068	chr2:98205859-98205860	Active TSS Weak transcription	Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
7	rs144857350	chr2:98205882-98205883	Active TSS Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	mRNA abundance
8	rs528964047	chr2:98205887-98205888	Active TSS Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
9	rs74177639	chr2:98205924-98205925	Active TSS Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	mRNA abundance
10	rs542767678	chr2:98205925-98205926	Active TSS Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
11	rs185401750	chr2:98206012-98206013	Active TSS Flanking Active TSS Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
12	rs188661236	chr2:98206013-98206014	Active TSS Flanking Active TSS Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
13	rs367931009	chr2:98206050-98206051	Active TSS Flanking Active TSS Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
14	rs2309264	chr2:98206060-98206061	Active TSS Flanking Active TSS Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
15	rs4069655	chr2:98206105-98206106	Active TSS Flanking Active TSS Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
16	rs2309265	chr2:98206106-98206107	Active TSS Flanking Active TSS Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
17	rs2309266	chr2:98206110-98206111	Active TSS Flanking Active TSS Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
18	rs551779525	chr2:98206158-98206159	Active TSS Flanking Active TSS Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
19	rs2871168	chr2:98206172-98206173	Active TSS Flanking Active TSS Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
20	rs571958025	chr2:98206176-98206177	Active TSS Flanking Active TSS Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
21	rs2309267	chr2:98206183-98206184	Active TSS Flanking Active TSS Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
22	rs1868445	chr2:98206188-98206189	Active TSS Flanking Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
23	rs117911431	chr2:98206189-98206190	Active TSS Flanking Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
24	rs181403494	chr2:98206193-98206194	Active TSS Flanking Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
25	rs553051845	chr2:98206216-98206217	Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
26	rs565696308	chr2:98206220-98206221	Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
27	rs537026595	chr2:98206243-98206244	Active TSS Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
28	rs28415903	chr2:98206282-98206283	Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
29	rs185739345	chr2:98206283-98206284	Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
30	rs375849557	chr2:98206284-98206285	Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
31	rs1814506	chr2:98206289-98206290	Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
32	rs76987115	chr2:98206291-98206292	Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
33	rs1814505	chr2:98206293-98206294	Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
34	rs3896685	chr2:98206320-98206321	Active TSS Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
35	rs368969039	chr2:98206355-98206356	Active TSS Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
36	rs573684603	chr2:98206381-98206382	Active TSS Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
37	rs370546211	chr2:98206408-98206409	Active TSS Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
38	rs3866776	chr2:98206429-98206430	Active TSS Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
39	rs573357099	chr2:98206459-98206460	Active TSS Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
40	rs545608093	chr2:98206478-98206479	Active TSS Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
41	rs377058746	chr2:98206546-98206547	Active TSS Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
42	rs4069656	chr2:98206563-98206564	Active TSS Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
43	rs4069657	chr2:98206621-98206622	Active TSS Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
44	rs531073896	chr2:98206646-98206647	Active TSS Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
45	rs550882097	chr2:98206660-98206661	Active TSS Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
46	rs560900526	chr2:98206695-98206696	Active TSS Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
47	rs188099446	chr2:98206705-98206706	Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
48	rs111575284	chr2:98206951-98206952	Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
49	rs546678628	chr2:98206960-98206961	Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
50	rs567001012	chr2:98206981-98206982	Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:52)

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
Chronic lymphocytic leukemia	21546498	CNVD
Tetralogy of Fallot	22912587	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:218 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:98143600-98205600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
2	chr2:98156200-98205600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
3	chr2:98160200-98205800	Weak transcription	K562	blood
4	chr2:98166400-98205600	Weak transcription	Brain Germinal Matrix	brain
5	chr2:98168400-98205800	Weak transcription	Fetal Lung	lung
6	chr2:98168400-98205800	Weak transcription	Fetal Muscle Trunk	muscle
7	chr2:98168600-98206000	Weak transcription	NHDF-Ad	bronchial
8	chr2:98169600-98205800	Weak transcription	Fetal Intestine Large	intestine
9	chr2:98171600-98205800	Weak transcription	Primary B cells from peripheral blood	blood
10	chr2:98172200-98205600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
11	chr2:98172200-98205800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
12	chr2:98172200-98205800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
13	chr2:98172200-98205800	Weak transcription	Duodenum Mucosa	Duodenum
14	chr2:98172200-98206000	Weak transcription	Brain Cingulate Gyrus	brain
15	chr2:98172400-98206000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
16	chr2:98173400-98205600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
17	chr2:98173400-98205800	Weak transcription	Primary monocytes fromperipheralblood	blood
18	chr2:98173400-98206000	Weak transcription	Primary T cells from cord blood	blood
19	chr2:98175000-98205800	Weak transcription	Adipose Nuclei	Adipose
20	chr2:98175200-98205600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
21	chr2:98175200-98205600	Weak transcription	Monocytes-CD14+_RO01746	blood
22	chr2:98175200-98206000	Weak transcription	Skeletal Muscle Female	skeletal muscle
23	chr2:98176200-98205800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
24	chr2:98176400-98205600	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
25	chr2:98177000-98205800	Weak transcription	HUES64 Cell Line	embryonic stem cell
26	chr2:98177000-98205800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
27	chr2:98177200-98205800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
28	chr2:98187400-98206000	Weak transcription	Brain Anterior Caudate	brain
29	chr2:98188600-98205600	Weak transcription	Fetal Stomach	stomach
30	chr2:98193800-98205800	Weak transcription	Brain Inferior Temporal Lobe	brain
31	chr2:98193800-98205800	Weak transcription	Stomach Smooth Muscle	stomach
32	chr2:98193800-98205800	Weak transcription	NH-A	brain
33	chr2:98194000-98205800	Weak transcription	HSMM	muscle
34	chr2:98194800-98205800	Weak transcription	HUES48 Cell Line	embryonic stem cell
35	chr2:98195000-98205800	Weak transcription	HepG2	liver
36	chr2:98196600-98205800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
37	chr2:98196800-98205600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
38	chr2:98196800-98205800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
39	chr2:98197000-98205800	Weak transcription	Primary T cells fromperipheralblood	blood
40	chr2:98197000-98205800	Weak transcription	Rectal Mucosa Donor 29	rectum
41	chr2:98199800-98205800	Weak transcription	NHEK	skin
42	chr2:98204800-98205600	Weak transcription	Primary T helper cells PMA-I stimulated	--
43	chr2:98204800-98205600	Weak transcription	Fetal Brain Female	brain
44	chr2:98204800-98205800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
45	chr2:98204800-98205800	Weak transcription	Primary T helper cells fromperipheralblood	blood
46	chr2:98204800-98206000	Weak transcription	Primary neutrophils fromperipheralblood	blood
47	chr2:98204800-98206000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
48	chr2:98204800-98207000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
49	chr2:98205000-98205200	Active TSS	Dnd41	blood
50	chr2:98205000-98205600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--

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