Variant report

Variant	esv3345187
Chromosome Location	chr2:98204545-98207093
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	BATF	chr2:98206281-98206755	GM12878	blood:	n/a	n/a
2	BATF	chr2:98206887-98207071	GM12878	blood:	n/a	n/a
3	BCL11A	chr2:98206444-98207010	GM12878	blood:	n/a	chr2:98206849-98206862 chr2:98206762-98206775
4	BCL11A	chr2:98205341-98205570	GM12878	blood:	n/a	n/a
5	BHLHE40	chr2:98206265-98206289	GM12878	blood:	n/a	n/a
6	BHLHE40	chr2:98206179-98206453	K562	blood:	n/a	n/a
7	BHLHE40	chr2:98206228-98206632	HepG2	liver:	n/a	n/a
8	CBX3	chr2:98206107-98207533	K562	blood:	n/a	n/a
9	CBX3	chr2:98206082-98206466	K562	blood:	n/a	n/a
10	CCNT2	chr2:98206271-98206359	K562	blood:	n/a	n/a
11	CEBPD	chr2:98206159-98206391	HepG2	liver:	n/a	n/a
12	CHD2	chr2:98206306-98206498	Hela-S3	cervix:	n/a	n/a
13	CHD2	chr2:98206243-98206454	K562	blood:	n/a	n/a
14	CHD2	chr2:98206316-98206476	HepG2	liver:	n/a	n/a
15	CTCF	chr2:98206689-98206995	GM13977	blood:	n/a	chr2:98206933-98206946 chr2:98206828-98206841
16	CTCF	chr2:98206620-98206770	GM12873	blood:	n/a	n/a
17	CTCF	chr2:98206683-98207112	LNCaP	prostate:	n/a	chr2:98206933-98206946 chr2:98206828-98206841
18	CTCF	chr2:98207080-98207230	AG04449	skin:	n/a	n/a
19	CTCF	chr2:98206628-98206979	K562	blood:	n/a	chr2:98206933-98206946 chr2:98206828-98206841
20	CTCF	chr2:98206237-98207868	A549	lung:	n/a	chr2:98207475-98207496 chr2:98206933-98206946 chr2:98207416-98207437 chr2:98207473-98207491 chr2:98206828-98206841 chr2:98207419-98207427 chr2:98207474-98207490 chr2:98207414-98207432
21	CTCF	chr2:98206653-98207055	Spleen_OC	spleen:	n/a	chr2:98206933-98206946 chr2:98206828-98206841
22	CTCF	chr2:98206713-98206940	GM13976	blood:	n/a	chr2:98206828-98206841
23	CTCF	chr2:98207000-98207150	RPTEC	kidney:	n/a	n/a
24	CTCF	chr2:98206614-98206957	GM12892	blood:	n/a	chr2:98206933-98206946 chr2:98206828-98206841
25	CTCF	chr2:98206705-98206933	GM12878	blood:	n/a	chr2:98206828-98206841
26	CTCF	chr2:98206980-98207130	WI-38	lung:	n/a	n/a
27	CTCF	chr2:98207080-98207230	Caco-2	colon:	n/a	n/a
28	CTCF	chr2:98207090-98207614	GM10266	blood:	n/a	chr2:98207475-98207496 chr2:98207416-98207437 chr2:98207473-98207491 chr2:98207419-98207427 chr2:98207474-98207490 chr2:98207414-98207432
29	CTCF	chr2:98206663-98207012	GM10248	blood:	n/a	chr2:98206933-98206946 chr2:98206828-98206841
30	CTCF	chr2:98206648-98206955	GM12891	blood:	n/a	chr2:98206933-98206946 chr2:98206828-98206841
31	CTCF	chr2:98207059-98207624	Gliobla	brain:	n/a	chr2:98207475-98207496 chr2:98207416-98207437 chr2:98207473-98207491 chr2:98207419-98207427 chr2:98207474-98207490 chr2:98207414-98207432
32	CTCF	chr2:98207003-98207009	Kidney_OC	kidney:	n/a	n/a
33	CTCF	chr2:98206705-98206960	Pancreas_OC	pancreas:	n/a	chr2:98206933-98206946 chr2:98206828-98206841
34	CTCF	chr2:98206681-98206954	MCF-7	breast:	n/a	chr2:98206933-98206946 chr2:98206828-98206841
35	CTCF	chr2:98206227-98207748	K562	blood:	n/a	chr2:98207475-98207496 chr2:98206933-98206946 chr2:98207416-98207437 chr2:98207473-98207491 chr2:98206828-98206841 chr2:98207419-98207427 chr2:98207474-98207490 chr2:98207414-98207432
36	CTCF	chr2:98206711-98206945	Lung_OC	lung:	n/a	chr2:98206828-98206841
37	CTCF	chr2:98206657-98206956	GM19240	blood:	n/a	chr2:98206933-98206946 chr2:98206828-98206841
38	CTCF	chr2:98206968-98207791	A549	lung:	n/a	chr2:98207475-98207496 chr2:98207416-98207437 chr2:98207473-98207491 chr2:98207419-98207427 chr2:98207474-98207490 chr2:98207414-98207432
39	CTCF	chr2:98207080-98207230	SK-N-SH_RA	brain:	n/a	n/a
40	CTCF	chr2:98206560-98206710	GM12866	blood:	n/a	n/a
41	CTCF	chr2:98207060-98207210	SK-N-SH_RA	brain:	n/a	n/a
42	CTCF	chr2:98206747-98206918	LNCaP	prostate:	n/a	chr2:98206828-98206841
43	CTCF	chr2:98207020-98207170	GM12870	blood:	n/a	n/a
44	CTCF	chr2:98206650-98206960	MCF-7	breast:	n/a	chr2:98206933-98206946 chr2:98206828-98206841
45	CTCF	chr2:98206775-98206872	HUVEC	blood vessel:	n/a	chr2:98206828-98206841
46	CTCF	chr2:98206601-98206989	A549	lung:	n/a	chr2:98206933-98206946 chr2:98206828-98206841
47	CTCF	chr2:98206740-98206881	HepG2	liver:	n/a	chr2:98206828-98206841
48	CTCF	chr2:98206608-98206984	Gliobla	brain:	n/a	chr2:98206933-98206946 chr2:98206828-98206841
49	CTCF	chr2:98206668-98206965	GM19238	blood:	n/a	chr2:98206933-98206946 chr2:98206828-98206841
50	CTCF	chr2:98206671-98206936	NHEK	skin:	n/a	chr2:98206828-98206841

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:98206249-98206299	AG04450	lung:	fetal
2	chr2:98206175-98206225	GM12892	blood:	n/a
3	chr2:98206249-98206299	HNPCEpiC	eye:	n/a
4	chr2:98206095-98206145	HAEpiC	amniotic membrane:	n/a
5	chr2:98206095-98206145	PrEC	prostate:	n/a
6	chr2:98206175-98206225	HCT-116	colon:	n/a
7	chr2:98206249-98206299	GM06990	blood:	n/a
8	chr2:98206733-98206783	AG10803	skin:	n/a
9	chr2:98206249-98206299	HAEpiC	amniotic membrane:	n/a
10	chr2:98206095-98206145	SK-N-SH	brain:	n/a
11	chr2:98206702-98206752	Caco-2	colon:	n/a
12	chr2:98206095-98206145	BE2_C	brain:	n/a
13	chr2:98206175-98206225	Caco-2	colon:	n/a
14	chr2:98206733-98206783	Jurkat	blood:	n/a
15	chr2:98206095-98206145	SK-N-MC	brain:	n/a
16	chr2:98206249-98206299	NH-A	brain:	n/a
17	chr2:98206095-98206145	HUVEC	blood vessel:	n/a
18	chr2:98205903-98205953	Hepatocyte	liver:	n/a
19	chr2:98205903-98205953	HEEpiC	esophagus:	n/a
20	chr2:98206095-98206145	GM19239	blood:	n/a
21	chr2:98205903-98205953	MCF10A-Er-Src	breast:	n/a
22	chr2:98206095-98206145	CMK	blood:	n/a
23	chr2:98206733-98206783	NHBE	bronchial:	n/a
24	chr2:98206733-98206783	BJ	skin:	n/a
25	chr2:98206702-98206752	Jurkat	blood:	n/a
26	chr2:98205903-98205953	PrEC	prostate:	n/a
27	chr2:98206702-98206752	CMK	blood:	n/a
28	chr2:98206249-98206299	SAEC	small airway:	n/a
29	chr2:98206733-98206783	HCPEpiC	choroid plexus:	n/a
30	chr2:98205903-98205953	HCT-116	colon:	n/a
31	chr2:98206175-98206225	NT2-D1	testis:	n/a
32	chr2:98206733-98206783	PANC-1	pancreas:	n/a
33	chr2:98206702-98206752	BJ	skin:	n/a
34	chr2:98206175-98206225	CMK	blood:	n/a
35	chr2:98206175-98206225	IMR90	lung:	fetal
36	chr2:98205903-98205953	NT2-D1	testis:	n/a
37	chr2:98206733-98206783	H1-hESC	embryonic stem cell:	embryo
38	chr2:98206175-98206225	NHDF-neo	bronchial:	n/a
39	chr2:98206175-98206225	HCPEpiC	choroid plexus:	n/a
40	chr2:98206175-98206225	BE2_C	brain:	n/a
41	chr2:98206733-98206783	Hepatocyte	liver:	n/a
42	chr2:98206249-98206299	HRE	kidney:	n/a
43	chr2:98206733-98206783	HMEC	breast:	n/a
44	chr2:98205903-98205953	CMK	blood:	n/a
45	chr2:98205903-98205953	LNCaP	prostate:	n/a
46	chr2:98206733-98206783	CMK	blood:	n/a
47	chr2:98206702-98206752	AG09319	gingival:	n/a
48	chr2:98206095-98206145	HEEpiC	esophagus:	n/a
49	chr2:98206175-98206225	MCF-7	breast:	n/a
50	chr2:98206095-98206145	NT2-D1	testis:	n/a

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

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

Extended variants
information (count: 72 )
Associated
traits (count: 52 )

Variant overlapped rSNPs/rCNVs (count:72 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs201946806	chr2:98204559-98204560	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs199998089	chr2:98204572-98204573	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs566293237	chr2:98204594-98204595	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs528753647	chr2:98204629-98204630	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs552055454	chr2:98204656-98204657	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs565647615	chr2:98204674-98204675	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs368727350	chr2:98204695-98204696	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs571513448	chr2:98204726-98204727	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs537496405	chr2:98204766-98204767	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs557029654	chr2:98204769-98204770	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs191301882	chr2:98204786-98204787	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs185446281	chr2:98204801-98204802	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs142370364	chr2:98204806-98204807	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs555106568	chr2:98204823-98204824	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs572225654	chr2:98204842-98204843	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs80029003	chr2:98204864-98204865	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs200943224	chr2:98204941-98204942	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs558041109	chr2:98205012-98205013	Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs577556188	chr2:98205016-98205017	Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs547812742	chr2:98205019-98205020	Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs201917219	chr2:98205243-98205244	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs3866780	chr2:98205416-98205417	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs1809113	chr2:98205724-98205725	Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs1814508	chr2:98205744-98205745	Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs563999457	chr2:98205799-98205800	Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs2924068	chr2:98205859-98205860	Active TSS Weak transcription	Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
27	rs144857350	chr2:98205882-98205883	Active TSS Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	mRNA abundance
28	rs528964047	chr2:98205887-98205888	Active TSS Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
29	rs74177639	chr2:98205924-98205925	Active TSS Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	mRNA abundance
30	rs542767678	chr2:98205925-98205926	Active TSS Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
31	rs185401750	chr2:98206012-98206013	Active TSS Flanking Active TSS Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
32	rs188661236	chr2:98206013-98206014	Active TSS Flanking Active TSS Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
33	rs367931009	chr2:98206050-98206051	Active TSS Flanking Active TSS Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
34	rs2309264	chr2:98206060-98206061	Active TSS Flanking Active TSS Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
35	rs4069655	chr2:98206105-98206106	Active TSS Flanking Active TSS Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
36	rs2309265	chr2:98206106-98206107	Active TSS Flanking Active TSS Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
37	rs2309266	chr2:98206110-98206111	Active TSS Flanking Active TSS Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
38	rs551779525	chr2:98206158-98206159	Active TSS Flanking Active TSS Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
39	rs2871168	chr2:98206172-98206173	Active TSS Flanking Active TSS Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
40	rs571958025	chr2:98206176-98206177	Active TSS Flanking Active TSS Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
41	rs2309267	chr2:98206183-98206184	Active TSS Flanking Active TSS Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
42	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
43	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
44	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
45	rs553051845	chr2:98206216-98206217	Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
46	rs565696308	chr2:98206220-98206221	Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
47	rs537026595	chr2:98206243-98206244	Active TSS Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
48	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
49	rs185739345	chr2:98206283-98206284	Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
50	rs375849557	chr2:98206284-98206285	Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	6 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:221 , 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	chr2:98164000-98204600	Weak transcription	A549	lung
5	chr2:98166400-98205600	Weak transcription	Brain Germinal Matrix	brain
6	chr2:98168400-98205800	Weak transcription	Fetal Lung	lung
7	chr2:98168400-98205800	Weak transcription	Fetal Muscle Trunk	muscle
8	chr2:98168600-98206000	Weak transcription	NHDF-Ad	bronchial
9	chr2:98169600-98205800	Weak transcription	Fetal Intestine Large	intestine
10	chr2:98171600-98205800	Weak transcription	Primary B cells from peripheral blood	blood
11	chr2:98172200-98205600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
12	chr2:98172200-98205800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
13	chr2:98172200-98205800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
14	chr2:98172200-98205800	Weak transcription	Duodenum Mucosa	Duodenum
15	chr2:98172200-98206000	Weak transcription	Brain Cingulate Gyrus	brain
16	chr2:98172400-98204600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
17	chr2:98172400-98206000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
18	chr2:98173400-98205600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
19	chr2:98173400-98205800	Weak transcription	Primary monocytes fromperipheralblood	blood
20	chr2:98173400-98206000	Weak transcription	Primary T cells from cord blood	blood
21	chr2:98175000-98205800	Weak transcription	Adipose Nuclei	Adipose
22	chr2:98175200-98205600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
23	chr2:98175200-98205600	Weak transcription	Monocytes-CD14+_RO01746	blood
24	chr2:98175200-98206000	Weak transcription	Skeletal Muscle Female	skeletal muscle
25	chr2:98176200-98205800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
26	chr2:98176400-98205600	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
27	chr2:98177000-98204600	Weak transcription	Muscle Satellite Cultured Cells	--
28	chr2:98177000-98205800	Weak transcription	HUES64 Cell Line	embryonic stem cell
29	chr2:98177000-98205800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
30	chr2:98177200-98205800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
31	chr2:98187400-98206000	Weak transcription	Brain Anterior Caudate	brain
32	chr2:98188600-98205600	Weak transcription	Fetal Stomach	stomach
33	chr2:98193800-98205800	Weak transcription	Brain Inferior Temporal Lobe	brain
34	chr2:98193800-98205800	Weak transcription	Stomach Smooth Muscle	stomach
35	chr2:98193800-98205800	Weak transcription	NH-A	brain
36	chr2:98194000-98205800	Weak transcription	HSMM	muscle
37	chr2:98194600-98204600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
38	chr2:98194800-98205800	Weak transcription	HUES48 Cell Line	embryonic stem cell
39	chr2:98195000-98205800	Weak transcription	HepG2	liver
40	chr2:98196600-98205800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
41	chr2:98196800-98204600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
42	chr2:98196800-98205600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
43	chr2:98196800-98205800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
44	chr2:98197000-98205800	Weak transcription	Primary T cells fromperipheralblood	blood
45	chr2:98197000-98205800	Weak transcription	Rectal Mucosa Donor 29	rectum
46	chr2:98199800-98205800	Weak transcription	NHEK	skin
47	chr2:98203800-98205000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
48	chr2:98203800-98205000	Active TSS	HUVEC	blood vessel
49	chr2:98204200-98204600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
50	chr2:98204200-98204800	Enhancers	Primary T helper memory cells from peripheral blood 2	blood

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