Variant report

Variant	nsv882412
Chromosome Location	chr5:97796120-97953719
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	chr5:97840348-97840659	HepG2	liver:	n/a	n/a
2	BHLHE40	chr5:97913597-97913623	GM12878	blood:	n/a	n/a
3	BHLHE40	chr5:97912432-97912625	K562	blood:	n/a	n/a
4	CEBPB	chr5:97810486-97810843	Hela-S3	cervix:	n/a	chr5:97810648-97810659
5	CEBPB	chr5:97810499-97810836	H1-hESC	embryonic stem cell:	n/a	chr5:97810648-97810659
6	CEBPB	chr5:97939819-97940054	HepG2	liver:	n/a	chr5:97939901-97939912
7	CEBPB	chr5:97801334-97801412	HepG2	liver:	n/a	n/a
8	CEBPB	chr5:97934761-97935081	Hela-S3	cervix:	n/a	chr5:97934933-97934946 chr5:97934933-97934944 chr5:97934935-97934944 chr5:97934933-97934946 chr5:97934935-97934944 chr5:97934934-97934945 chr5:97934935-97934944 chr5:97934935-97934944
9	CEBPB	chr5:97810587-97810749	HepG2	liver:	n/a	chr5:97810648-97810659
10	CEBPB	chr5:97797189-97797660	A549	lung:	n/a	n/a
11	CEBPB	chr5:97810486-97810851	ECC-1	luminal epithelium:	n/a	chr5:97810648-97810659
12	CEBPB	chr5:97810464-97810843	IMR90	lung:	n/a	chr5:97810648-97810659
13	CEBPB	chr5:97807135-97807430	IMR90	lung:	n/a	chr5:97807290-97807301
14	CEBPB	chr5:97807160-97807430	HepG2	liver:	n/a	chr5:97807290-97807301
15	CEBPB	chr5:97900102-97900172	A549	lung:	n/a	chr5:97900113-97900124
16	CEBPB	chr5:97810475-97810832	A549	lung:	n/a	chr5:97810648-97810659
17	CEBPB	chr5:97874291-97874538	HepG2	liver:	n/a	chr5:97874401-97874412
18	CEBPB	chr5:97892415-97892773	IMR90	lung:	n/a	n/a
19	CEBPB	chr5:97810464-97810846	HepG2	liver:	n/a	chr5:97810648-97810659
20	CEBPB	chr5:97810456-97810914	A549	lung:	n/a	chr5:97810648-97810659
21	CEBPB	chr5:97934708-97935043	MCF-7	breast:	n/a	chr5:97934933-97934946 chr5:97934933-97934944 chr5:97934935-97934944 chr5:97934933-97934946 chr5:97934935-97934944 chr5:97934934-97934945 chr5:97934935-97934944 chr5:97934935-97934944
22	CEBPB	chr5:97934734-97935106	HepG2	liver:	n/a	chr5:97934933-97934946 chr5:97934933-97934944 chr5:97935095-97935103 chr5:97934935-97934944 chr5:97934933-97934946 chr5:97934935-97934944 chr5:97934934-97934945 chr5:97934935-97934944 chr5:97934935-97934944
23	CEBPB	chr5:97810520-97810893	MCF-7	breast:	n/a	chr5:97810648-97810659
24	CEBPB	chr5:97934745-97935054	A549	lung:	n/a	chr5:97934933-97934946 chr5:97934933-97934944 chr5:97934935-97934944 chr5:97934933-97934946 chr5:97934935-97934944 chr5:97934934-97934945 chr5:97934935-97934944 chr5:97934935-97934944
25	CEBPB	chr5:97797235-97797557	IMR90	lung:	n/a	n/a
26	CEBPB	chr5:97797272-97797669	HepG2	liver:	n/a	n/a
27	CEBPB	chr5:97934750-97935110	A549	lung:	n/a	chr5:97934933-97934946 chr5:97934933-97934944 chr5:97935095-97935103 chr5:97934935-97934944 chr5:97934933-97934946 chr5:97934935-97934944 chr5:97934934-97934945 chr5:97934935-97934944 chr5:97934935-97934944
28	CEBPB	chr5:97810486-97810835	K562	blood:	n/a	chr5:97810648-97810659
29	CEBPB	chr5:97934743-97935117	IMR90	lung:	n/a	chr5:97934933-97934946 chr5:97934933-97934944 chr5:97935095-97935103 chr5:97934935-97934944 chr5:97934933-97934946 chr5:97934935-97934944 chr5:97934934-97934945 chr5:97934935-97934944 chr5:97934935-97934944
30	CEBPB	chr5:97934752-97935098	H1-hESC	embryonic stem cell:	n/a	chr5:97934933-97934946 chr5:97934933-97934944 chr5:97934935-97934944 chr5:97934933-97934946 chr5:97934935-97934944 chr5:97934934-97934945 chr5:97934935-97934944 chr5:97934935-97934944
31	CEBPB	chr5:97900029-97900266	HepG2	liver:	n/a	chr5:97900113-97900124
32	CEBPB	chr5:97900586-97900903	IMR90	lung:	n/a	chr5:97900726-97900737 chr5:97900724-97900737
33	CEBPB	chr5:97810441-97810814	HepG2	liver:	n/a	chr5:97810648-97810659
34	CEBPB	chr5:97934775-97935102	K562	blood:	n/a	chr5:97934933-97934946 chr5:97934933-97934944 chr5:97934935-97934944 chr5:97934933-97934946 chr5:97934935-97934944 chr5:97934934-97934945 chr5:97934935-97934944 chr5:97934935-97934944
35	CHD2	chr5:97913543-97913562	GM12878	blood:	n/a	n/a
36	CTCF	chr5:97836500-97836650	HCM	heart:	n/a	n/a
37	CTCF	chr5:97912515-97912683	HepG2	liver:	n/a	n/a
38	CTCF	chr5:97912400-97912550	HA-sp	spinal cord:	n/a	n/a
39	CTCF	chr5:97850100-97850250	NHLF	lung:	n/a	n/a
40	CTCF	chr5:97839360-97839510	HAc	cerebellar:	n/a	n/a
41	CTCF	chr5:97912440-97912590	GM12874	blood:	n/a	n/a
42	CTCF	chr5:97912440-97912590	HBMEC	blood vessel:	n/a	n/a
43	CTCF	chr5:97940920-97941070	HCPEpiC	choroid plexus:	n/a	chr5:97941006-97941024 chr5:97941008-97941029 chr5:97941009-97941017
44	CTCF	chr5:97831933-97831992	LNCaP	prostate:	n/a	n/a
45	CTCF	chr5:97912480-97912630	GM12867	blood:	n/a	n/a
46	CTCF	chr5:97912320-97912470	GM12873	blood:	n/a	n/a
47	CTCF	chr5:97912087-97912136	MCF-7	breast:	n/a	n/a
48	CTCF	chr5:97948600-97948750	HEEpiC	esophagus:	n/a	n/a
49	CTCF	chr5:97820160-97820310	BE2_C	brain:	n/a	n/a
50	CTCF	chr5:97912398-97912784	Medullo	brain:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:97949352-97949402	Hepatocyte	liver:	n/a
2	chr5:97873389-97873439	T-47D	breast:	n/a
3	chr5:97839561-97839611	GM19239	blood:	n/a
4	chr5:97912653-97912703	U87	brain:	n/a
5	chr5:97912185-97912235	PFSK-1	brain:	n/a
6	chr5:97949352-97949402	Hepatocyte	liver:	n/a
7	chr5:97873389-97873439	T-47D	breast:	n/a
8	chr5:97839561-97839611	GM19239	blood:	n/a
9	chr5:97912653-97912703	U87	brain:	n/a
10	chr5:97912185-97912235	PFSK-1	brain:	n/a
11	chr5:97833812-97833862	NHBE	bronchial:	n/a
12	chr5:97882639-97882689	GM12878	blood:	n/a
13	chr5:97882690-97882740	AG10803	skin:	n/a
14	chr5:97839561-97839611	SAEC	small airway:	n/a
15	chr5:97912653-97912703	BE2_C	brain:	n/a
16	chr5:97903451-97903501	H1-hESC	embryonic stem cell:	embryo
17	chr5:97912653-97912703	A549	lung:	n/a
18	chr5:97882639-97882689	PrEC	prostate:	n/a
19	chr5:97833812-97833862	NB4	blood:	n/a
20	chr5:97912440-97912490	AG10803	skin:	n/a
21	chr5:97873389-97873439	BJ	skin:	n/a
22	chr5:97949352-97949402	HL-60	blood:	n/a
23	chr5:97912931-97912981	AG09309	skin:	n/a
24	chr5:97912440-97912490	HEK293	kidney:	embryo
25	chr5:97882639-97882689	AG09309	skin:	n/a
26	chr5:97892898-97892948	BJ	skin:	n/a
27	chr5:97949352-97949402	Hela-S3	cervix:	n/a
28	chr5:97912440-97912490	NHBE	bronchial:	n/a
29	chr5:97903451-97903501	Jurkat	blood:	n/a
30	chr5:97892898-97892948	K562	blood:	n/a
31	chr5:97839561-97839611	Jurkat	blood:	n/a
32	chr5:97839561-97839611	AG10803	skin:	n/a
33	chr5:97903451-97903501	HL-60	blood:	n/a
34	chr5:97912440-97912490	HCT-116	colon:	n/a
35	chr5:97892898-97892948	HUVEC	blood vessel:	n/a
36	chr5:97949352-97949402	GM12878	blood:	n/a
37	chr5:97882690-97882740	HPAEpiC	pulmonary alveolar:	n/a
38	chr5:97949352-97949402	HRE	kidney:	n/a
39	chr5:97833812-97833862	GM12878	blood:	n/a
40	chr5:97949352-97949402	BE2_C	brain:	n/a
41	chr5:97833812-97833862	HepG2	liver:	n/a
42	chr5:97882690-97882740	GM19239	blood:	n/a
43	chr5:97833812-97833862	HCT-116	colon:	n/a
44	chr5:97912653-97912703	HCM	heart:	n/a
45	chr5:97873389-97873439	HRCEpiC	kidney:	n/a
46	chr5:97903451-97903501	NHBE	bronchial:	n/a
47	chr5:97873389-97873439	LNCaP	prostate:	n/a
48	chr5:97882690-97882740	AoSMC	blood vessel:	n/a
49	chr5:97912185-97912235	SK-N-SH_RA	brain:	n/a
50	chr5:97912185-97912235	AG09319	gingival:	n/a

No.	Distal block	Cell Line	Cell type
1	chr5:97947803..97949307-chr5:97953669..97956460,2	K562	blood:
2	chr5:97899000..97899520-chr6:119558658..119559166,2	MCF-7	breast:
3	chr5:97927782..97929943-chr5:97931809..97933564,2	K562	blood:
4	chr5:97927404..97929282-chr5:97932064..97934664,2	K562	blood:
5	chr5:97947803..97949307-chr5:97953669..97956460,2	K562	blood:
6	chr5:97849489..97851225-chr5:97851628..97853211,2	MCF-7	breast:
7	chr5:97927782..97929943-chr5:97931809..97933564,2	K562	blood:
8	chr5:97849489..97851225-chr5:97851628..97853211,2	MCF-7	breast:
9	chr5:97880735..97882855-chr5:98107997..98110735,2	MCF-7	breast:
10	chr5:97927404..97929282-chr5:97932064..97934664,2	K562	blood:

Variant related genes	Relation type
CTBP2P4	TF binding region
CTBP2P4	CpG island
ENSG00000174136	chromatin interactions
ENSG00000246763	chromatin interactions

Extended variants
information (count: 5859 )
Associated
traits (count: 84 )

Variant overlapped rSNPs/rCNVs (count:5859 , 50 per page) page: 1 2 3 4 5 6 7 ... 118

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10463709	chr5:97796120-97796121	Strong transcription Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs558745205	chr5:97796166-97796167	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs114743000	chr5:97796224-97796225	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs538011476	chr5:97796302-97796303	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs184144940	chr5:97796313-97796314	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs144170267	chr5:97796384-97796385	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs187677455	chr5:97796440-97796441	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs191970593	chr5:97796467-97796468	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs541893154	chr5:97796622-97796623	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs149319052	chr5:97796695-97796696	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs144561865	chr5:97796731-97796732	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs545889241	chr5:97796746-97796747	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs564178699	chr5:97796802-97796803	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs148033977	chr5:97796806-97796807	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs74644282	chr5:97796832-97796833	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs575220767	chr5:97796846-97796847	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs73772950	chr5:97796892-97796893	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs529536879	chr5:97796908-97796909	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs553730997	chr5:97796910-97796911	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs142450675	chr5:97796917-97796918	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs564039151	chr5:97796935-97796936	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs143936295	chr5:97796956-97796957	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs555882730	chr5:97797037-97797038	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs533129829	chr5:97797051-97797052	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs551600118	chr5:97797064-97797065	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs376072897	chr5:97797117-97797118	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs147275434	chr5:97797118-97797119	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs537646486	chr5:97797124-97797125	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs556320878	chr5:97797130-97797131	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs200562701	chr5:97797190-97797191	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs535729162	chr5:97797194-97797195	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs553828023	chr5:97797245-97797246	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs572090731	chr5:97797279-97797280	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs545747144	chr5:97797289-97797290	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs557572178	chr5:97797333-97797334	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs376994508	chr5:97797360-97797361	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs576086546	chr5:97797377-97797378	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs140769044	chr5:97797437-97797438	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs562295211	chr5:97797448-97797449	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs529571269	chr5:97797456-97797457	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs541347889	chr5:97797465-97797466	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs559586096	chr5:97797515-97797516	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs533165703	chr5:97797598-97797599	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs113389056	chr5:97797639-97797640	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs144640920	chr5:97797647-97797648	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs10463714	chr5:97797651-97797652	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs549743964	chr5:97797666-97797667	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs568236946	chr5:97797685-97797686	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs112934688	chr5:97797711-97797712	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs370124377	chr5:97797714-97797715	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:84)

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
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
Glioblastoma multiforme	22286061	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Breast cancer	21611746	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:965 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:97790600-97799200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr5:97791600-97797600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
3	chr5:97791600-97797800	Enhancers	NHDF-Ad	bronchial
4	chr5:97791800-97799000	Weak transcription	HMEC	breast
5	chr5:97794800-97800400	Weak transcription	NHLF	lung
6	chr5:97795000-97804200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
7	chr5:97795400-97796400	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
8	chr5:97795600-97796400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
9	chr5:97795600-97797000	Enhancers	Osteobl	bone
10	chr5:97795800-97796800	Enhancers	HSMM	muscle
11	chr5:97795800-97796800	Enhancers	HSMMtube	muscle
12	chr5:97795800-97797000	Enhancers	Muscle Satellite Cultured Cells	--
13	chr5:97795800-97797400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
14	chr5:97796000-97796400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
15	chr5:97796000-97797200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
16	chr5:97796000-97800200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
17	chr5:97796400-97799600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
18	chr5:97796400-97800000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
19	chr5:97796400-97802400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
20	chr5:97796800-97797200	Weak transcription	HSMMtube	muscle
21	chr5:97797000-97800000	Weak transcription	Osteobl	bone
22	chr5:97797000-97802800	Weak transcription	Muscle Satellite Cultured Cells	--
23	chr5:97797200-97797400	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
24	chr5:97797200-97797400	Enhancers	HSMMtube	muscle
25	chr5:97797400-97800200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
26	chr5:97797400-97803400	Weak transcription	HSMMtube	muscle
27	chr5:97797400-97804400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
28	chr5:97797600-97799800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
29	chr5:97797800-97799600	Weak transcription	NHDF-Ad	bronchial
30	chr5:97799000-97800000	Enhancers	HMEC	breast
31	chr5:97799200-97799800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
32	chr5:97799200-97800000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
33	chr5:97799200-97800000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
34	chr5:97799200-97800000	Enhancers	NHEK	skin
35	chr5:97799600-97800200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
36	chr5:97799600-97800400	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
37	chr5:97799600-97802600	Enhancers	NHDF-Ad	bronchial
38	chr5:97799800-97800400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
39	chr5:97799800-97800800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
40	chr5:97800000-97800200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
41	chr5:97800000-97800600	Enhancers	Osteobl	bone
42	chr5:97800000-97803200	Weak transcription	HMEC	breast
43	chr5:97800000-97803400	Weak transcription	NHEK	skin
44	chr5:97800000-97803600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
45	chr5:97800000-97804400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
46	chr5:97800200-97800400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
47	chr5:97800200-97800400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
48	chr5:97800200-97801200	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
49	chr5:97800200-97801200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
50	chr5:97800400-97800800	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived

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