Variant report

Variant	esv2422224
Chromosome Location	chr5:96889331-97015454
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	ATF1	chr5:96925354-96925372	K562	blood:	n/a	n/a
2	BCL3	chr5:96928285-96928637	GM12878	blood:	n/a	n/a
3	CEBPB	chr5:96984114-96984366	A549	lung:	n/a	chr5:96984229-96984240
4	CEBPB	chr5:96889557-96889904	HepG2	liver:	n/a	chr5:96889732-96889743 chr5:96889717-96889728
5	CEBPB	chr5:96889560-96889890	A549	lung:	n/a	chr5:96889732-96889743 chr5:96889717-96889728
6	CEBPB	chr5:96889595-96889861	Hela-S3	cervix:	n/a	chr5:96889732-96889743 chr5:96889717-96889728
7	CEBPB	chr5:96984131-96984412	HepG2	liver:	n/a	chr5:96984229-96984240
8	CEBPB	chr5:96958462-96958749	HepG2	liver:	n/a	chr5:96958584-96958595 chr5:96958604-96958615
9	CEBPB	chr5:96958443-96958670	A549	lung:	n/a	chr5:96958584-96958595 chr5:96958604-96958615
10	CEBPB	chr5:96930445-96930679	IMR90	lung:	n/a	n/a
11	CEBPB	chr5:96889795-96889802	K562	blood:	n/a	n/a
12	CEBPB	chr5:96889539-96889927	IMR90	lung:	n/a	chr5:96889732-96889743 chr5:96889717-96889728
13	CEBPB	chr5:96928194-96928475	HepG2	liver:	n/a	chr5:96928315-96928326
14	CEBPB	chr5:96984266-96984278	K562	blood:	n/a	n/a
15	CEBPB	chr5:96916250-96916433	HepG2	liver:	n/a	chr5:96916265-96916273
16	CTCF	chr5:96970920-96971070	HCT-116	colon:	n/a	n/a
17	CTCF	chr5:96893511-96893533	Fibrobl	skin:	n/a	n/a
18	CTCF	chr5:96931564-96931659	Spleen_OC	spleen:	n/a	n/a
19	CTCF	chr5:96971000-96971150	GM12864	blood:	n/a	chr5:96971076-96971094 chr5:96971079-96971088
20	CTCF	chr5:96970980-96971130	HEK293	kidney:	n/a	chr5:96971076-96971094 chr5:96971079-96971088
21	CTCF	chr5:96971040-96971190	MCF-7	breast:	n/a	chr5:96971076-96971094 chr5:96971079-96971088
22	CTCF	chr5:96970980-96971130	GM12874	blood:	n/a	chr5:96971076-96971094 chr5:96971079-96971088
23	CTCF	chr5:96890680-96890830	AG04449	skin:	n/a	n/a
24	CTCF	chr5:96971020-96971170	MCF-7	breast:	n/a	chr5:96971076-96971094 chr5:96971079-96971088
25	CTCF	chr5:96970960-96971110	HPAF	blood vessel:	n/a	chr5:96971076-96971094 chr5:96971079-96971088
26	CTCF	chr5:96971020-96971170	HPAF	blood vessel:	n/a	chr5:96971076-96971094 chr5:96971079-96971088
27	CTCF	chr5:96970920-96971070	GM12866	blood:	n/a	n/a
28	CTCF	chr5:96959280-96959430	Caco-2	colon:	n/a	n/a
29	CTCF	chr5:96973533-96973572	GM20000	blood:	n/a	n/a
30	CTCF	chr5:96970980-96971130	HBMEC	blood vessel:	n/a	chr5:96971076-96971094 chr5:96971079-96971088
31	CTCF	chr5:96959320-96959464	H1-hESC	embryonic stem cell:	n/a	n/a
32	CTCF	chr5:96970960-96971110	GM12875	blood:	n/a	chr5:96971076-96971094 chr5:96971079-96971088
33	CTCF	chr5:96971000-96971150	HCPEpiC	choroid plexus:	n/a	chr5:96971076-96971094 chr5:96971079-96971088
34	CTCF	chr5:96971020-96971170	HCPEpiC	choroid plexus:	n/a	chr5:96971076-96971094 chr5:96971079-96971088
35	CTCF	chr5:96971020-96971170	HepG2	liver:	n/a	chr5:96971076-96971094 chr5:96971079-96971088
36	CTCF	chr5:97013600-97013750	HEEpiC	esophagus:	n/a	n/a
37	CTCF	chr5:96971040-96971190	Hela-S3	cervix:	n/a	chr5:96971076-96971094 chr5:96971079-96971088
38	CTCF	chr5:96893520-96893570	ProgFib	skin:	n/a	n/a
39	CTCF	chr5:96931526-96931573	Lung_OC	lung:	n/a	n/a
40	CTCF	chr5:96970980-96971130	GM12872	blood:	n/a	chr5:96971076-96971094 chr5:96971079-96971088
41	CTCF	chr5:96971040-96971190	HCFaa	heart:	n/a	chr5:96971076-96971094 chr5:96971079-96971088
42	CTCF	chr5:96971000-96971150	HMF	breast:	n/a	chr5:96971076-96971094 chr5:96971079-96971088
43	CTCF	chr5:96971055-96971077	MCF-7	breast:	n/a	n/a
44	CTCF	chr5:96970940-96971090	GM12872	blood:	n/a	chr5:96971079-96971088
45	CTCF	chr5:96971069-96971129	HepG2	liver:	n/a	chr5:96971076-96971094 chr5:96971079-96971088
46	CTCF	chr5:96959212-96959530	H1-hESC	embryonic stem cell:	n/a	n/a
47	CTCF	chr5:96971020-96971170	GM12873	blood:	n/a	chr5:96971076-96971094 chr5:96971079-96971088
48	CTCF	chr5:96971015-96971096	MCF-7	breast:	n/a	chr5:96971076-96971094 chr5:96971079-96971088
49	CTCF	chr5:96971120-96971270	GM12873	blood:	n/a	n/a
50	CTCF	chr5:96971040-96971190	GM12872	blood:	n/a	chr5:96971076-96971094 chr5:96971079-96971088

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:96890257-96890307	SKMC	muscle:	n/a
2	chr5:96915770-96915820	GM12891	blood:	n/a
3	chr5:96915770-96915820	IMR90	lung:	fetal
4	chr5:96915770-96915820	HNPCEpiC	eye:	n/a
5	chr5:96915770-96915820	MCF10A-Er-Src	breast:	n/a
6	chr5:96890257-96890307	ovcar-3	ovarian:	n/a
7	chr5:96890257-96890307	SK-N-MC	brain:	n/a
8	chr5:96890257-96890307	T-47D	breast:	n/a
9	chr5:96890257-96890307	AG04449	skin:	fetal
10	chr5:96890257-96890307	MCF-7	breast:	n/a
11	chr5:96915770-96915820	PANC-1	pancreas:	n/a
12	chr5:96890257-96890307	HL-60	blood:	n/a
13	chr5:96915770-96915820	BJ	skin:	n/a
14	chr5:96915770-96915820	SKMC	muscle:	n/a
15	chr5:96890257-96890307	PANC-1	pancreas:	n/a
16	chr5:96890257-96890307	RPTEC	kidney:	n/a
17	chr5:96915770-96915820	ECC-1	luminal epithelium:	n/a
18	chr5:96890257-96890307	HMEC	breast:	n/a
19	chr5:96890257-96890307	CMK	blood:	n/a
20	chr5:96915770-96915820	GM19239	blood:	n/a
21	chr5:96915770-96915820	PFSK-1	brain:	n/a
22	chr5:96890257-96890307	GM12878	blood:	n/a
23	chr5:96890257-96890307	HEEpiC	esophagus:	n/a
24	chr5:96890257-96890307	HIPEpiC	eye:	n/a
25	chr5:96890257-96890307	IMR90	lung:	fetal
26	chr5:96915770-96915820	AG04449	skin:	fetal
27	chr5:96890257-96890307	NHDF-neo	bronchial:	n/a
28	chr5:96915770-96915820	SAEC	small airway:	n/a
29	chr5:96915770-96915820	SK-N-SH	brain:	n/a
30	chr5:96890257-96890307	HCF	heart:	n/a
31	chr5:96915770-96915820	HCF	heart:	n/a
32	chr5:96890257-96890307	HRE	kidney:	n/a
33	chr5:96890257-96890307	ECC-1	luminal epithelium:	n/a
34	chr5:96915770-96915820	AG09319	gingival:	n/a
35	chr5:96915770-96915820	HUVEC	blood vessel:	n/a
36	chr5:96915770-96915820	NT2-D1	testis:	n/a
37	chr5:96890257-96890307	HPAEpiC	pulmonary alveolar:	n/a
38	chr5:96890257-96890307	NB4	blood:	n/a
39	chr5:96890257-96890307	A549	lung:	n/a
40	chr5:96915770-96915820	HCM	heart:	n/a
41	chr5:96890257-96890307	NHBE	bronchial:	n/a
42	chr5:96890257-96890307	GM19239	blood:	n/a
43	chr5:96915770-96915820	Hela-S3	cervix:	n/a
44	chr5:96915770-96915820	U87	brain:	n/a
45	chr5:96915770-96915820	HIPEpiC	eye:	n/a
46	chr5:96890257-96890307	SK-N-SH_RA	brain:	n/a
47	chr5:96890257-96890307	HCT-116	colon:	n/a
48	chr5:96915770-96915820	Jurkat	blood:	n/a
49	chr5:96890257-96890307	PrEC	prostate:	n/a
50	chr5:96915770-96915820	HEEpiC	esophagus:	n/a

No.	Distal block	Cell Line	Cell type
1	chr5:96898495..96900851-chr5:96905056..96906917,2	K562	blood:
2	chr5:96902855..96905560-chr5:96907320..96909656,2	K562	blood:
3	chr5:96902855..96905560-chr5:96907320..96909656,2	K562	blood:
4	chr5:96898495..96900851-chr5:96905056..96906917,2	K562	blood:
5	chr5:96987103..96987619-chr5:97253568..97254119,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CTD-2215E18.1.1-2	chr5:97006297-97006750	NONHSAT102931
2	lnc-CTD-2215E18.1.1-2	chr5:97004255-97004366	XLOC_004483
3	lnc-CTD-2215E18.1.1-2	chr5:97006298-97006750	XLOC_004483
4	lnc-CTD-2215E18.1.1-2	chr5:97004254-97004366	NONHSAT102931
5	lnc-CTD-2215E18.1.1-2	chr5:97004255-97004366	NR_105028
6	lnc-CTD-2215E18.1.1-2	chr5:97006298-97006755	NR_105028

Variant related genes	Relation type
ENSG00000248931	TF binding region
ENSG00000248931	CpG island

Extended variants
information (count: 2254 )
Associated
traits (count: 80 )

Variant overlapped rSNPs/rCNVs (count:2254 , 50 per page) page: 1 2 3 4 5 6 7 ... 46

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs142098939	chr5:96889361-96889362	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs557694954	chr5:96889394-96889395	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs78349072	chr5:96889436-96889437	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs113283345	chr5:96889528-96889529	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs375359274	chr5:96889529-96889530	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs114920764	chr5:96889546-96889547	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs547394837	chr5:96889549-96889550	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs555359686	chr5:96889575-96889576	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs573517191	chr5:96889613-96889614	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs540799515	chr5:96889632-96889633	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs373165681	chr5:96889637-96889638	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs10039876	chr5:96889737-96889738	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs17087581	chr5:96889770-96889771	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs545164037	chr5:96889811-96889812	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs190405944	chr5:96889899-96889900	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs183801518	chr5:96889992-96889993	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs563750924	chr5:96890084-96890085	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs73779163	chr5:96890093-96890094	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs376304694	chr5:96890113-96890114	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs549683131	chr5:96890139-96890140	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs151163410	chr5:96890176-96890177	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs188734483	chr5:96890208-96890209	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs547168945	chr5:96890210-96890211	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs539263706	chr5:96890250-96890251	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs140125633	chr5:96890265-96890266	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs146927811	chr5:96890268-96890269	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs539560033	chr5:96890296-96890297	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs538398667	chr5:96890315-96890316	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs138236621	chr5:96890377-96890378	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs569668087	chr5:96890396-96890397	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs193297166	chr5:96890418-96890419	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs112676634	chr5:96890430-96890431	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs555656655	chr5:96890447-96890448	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs116250590	chr5:96890454-96890455	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs540838461	chr5:96890477-96890478	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs552791607	chr5:96890481-96890482	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs577415471	chr5:96890520-96890521	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs76179256	chr5:96890541-96890542	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs142227151	chr5:96890566-96890567	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs530947456	chr5:96890577-96890578	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs145983107	chr5:96890594-96890595	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs575825418	chr5:96890597-96890598	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs113595861	chr5:96890617-96890618	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs35077933	chr5:96890687-96890688	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs187705917	chr5:96890780-96890781	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs571731340	chr5:96890792-96890793	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs138793420	chr5:96890846-96890847	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs191479772	chr5:96890869-96890870	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs374031306	chr5:96890930-96890931	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs76867017	chr5:96890955-96890956	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:80)

Disease	PMID	Source
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Metanephric adenoma	20802469	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Medulloblastoma	21979893	CNVD
Phyllodes tumor	17334353	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Cancer	16751803	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	17603634	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Melanoma	18172304	CNVD
Glioma	20126413	CNVD
Breast cancer	17393978	CNVD
Cancer	21359685	CNVD
Non-small cell lung cancer	21829676	CNVD
adenomatous polyposis	22470819	CNVD
Cancer	22429812	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Liposarcoma	21253554	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Breast cancer	21858162	CNVD
Leukemia	17361228	CNVD
Myelodysplastic syndrome	18508791	CNVD
5q-syndrome	17576883	CNVD
Gastric cancer	17908304	CNVD
Lung cancer	16740712	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Urothelial carcinoma	21177765	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Barrett''s syndrome	19417022	CNVD
Lung cancer	18438408	CNVD
Retinoblastoma	22278416	CNVD
Bipolar disorder	18458673	CNVD
Thyroid cancer	19087340	CNVD
Breast cancer	21785460	CNVD
Merkel cell carcinoma	19020549	CNVD
Squamous cell cancer	20885788	CNVD
Hepatocellular carcinoma	16750200	CNVD
Neurodevelopmental disorder	22521361	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	17133270	CNVD
Acute myeloid leukemia	20729466	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Acute myeloid leukemia	21251322	CNVD
lymphocytic leukemia	21291569	CNVD
Testicular cancer	18059402	CNVD
Colorectal cancer	16272173	CNVD
Prostate cancer	16573809	CNVD
Basal cell lymphoma	17053054	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Mental retardation	19471318	CNVD
Renal cell carcinoma	18194544	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Cancer	20164920	CNVD
Myelodysplastic syndrome	21251322	CNVD
abnormal development	18461090	CNVD
Myelofibrosis	22110671	CNVD
Colorectal cancer	16774939	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Multiple myeloma	17550852	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:210 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:96881000-96890000	Weak transcription	Fetal Muscle Leg	muscle
2	chr5:96882000-96889400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
3	chr5:96884400-96890400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
4	chr5:96884800-96889600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
5	chr5:96886000-96889400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
6	chr5:96886200-96889600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
7	chr5:96886200-96889800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
8	chr5:96886400-96889400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
9	chr5:96886400-96889400	Weak transcription	HSMM	muscle
10	chr5:96886400-96889800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
11	chr5:96886400-96889800	Weak transcription	Muscle Satellite Cultured Cells	--
12	chr5:96886400-96889800	Weak transcription	NHEK	skin
13	chr5:96886400-96889800	Weak transcription	Osteobl	bone
14	chr5:96886400-96890000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
15	chr5:96886600-96889400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
16	chr5:96886800-96889400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
17	chr5:96886800-96889600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
18	chr5:96888400-96891600	Enhancers	Cortex derived primary cultured neurospheres	brain
19	chr5:96889200-96891800	Enhancers	NHDF-Ad	bronchial
20	chr5:96889400-96891600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
21	chr5:96889400-96891600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
22	chr5:96889400-96891600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
23	chr5:96889400-96891600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
24	chr5:96889400-96891600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
25	chr5:96889400-96891600	Enhancers	HSMM	muscle
26	chr5:96889400-96891600	Enhancers	NHLF	lung
27	chr5:96889600-96890400	Enhancers	Breast Myoepithelial Primary Cells	Breast
28	chr5:96889600-96890400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
29	chr5:96889600-96891600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
30	chr5:96889800-96890800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
31	chr5:96889800-96890800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
32	chr5:96889800-96891200	Enhancers	NH-A	brain
33	chr5:96889800-96891400	Enhancers	HSMMtube	muscle
34	chr5:96889800-96891600	Enhancers	Muscle Satellite Cultured Cells	--
35	chr5:96889800-96891600	Enhancers	HMEC	breast
36	chr5:96889800-96891600	Enhancers	NHEK	skin
37	chr5:96889800-96891600	Enhancers	Osteobl	bone
38	chr5:96890000-96890400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
39	chr5:96890000-96890400	Enhancers	Primary hematopoietic stem cells	blood
40	chr5:96890000-96890600	Enhancers	ES-WA7 Cell Line	embryonic stem cell
41	chr5:96890000-96891200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
42	chr5:96890000-96891200	Enhancers	Fetal Muscle Leg	muscle
43	chr5:96890000-96891600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
44	chr5:96890400-96890800	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
45	chr5:96890400-96891200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
46	chr5:96890400-96895600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
47	chr5:96890600-96891000	Enhancers	Primary hematopoietic stem cells	blood
48	chr5:96890800-96896000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
49	chr5:96891200-96892400	Enhancers	Breast Myoepithelial Primary Cells	Breast
50	chr5:96891600-96894600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin

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