Variant report

Variant	esv3372859
Chromosome Location	chr5:97190949-97325577
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	ATF2	chr5:97224163-97224479	GM12878	blood:	n/a	n/a
2	ATF2	chr5:97224125-97224557	GM12878	blood:	n/a	n/a
3	BATF	chr5:97224123-97224497	GM12878	blood:	n/a	n/a
4	BATF	chr5:97224132-97224459	GM12878	blood:	n/a	n/a
5	BCL11A	chr5:97224140-97224399	GM12878	blood:	n/a	chr5:97224311-97224320
6	BCL11A	chr5:97259838-97260091	GM12878	blood:	n/a	n/a
7	BCL11A	chr5:97224159-97224505	GM12878	blood:	n/a	chr5:97224311-97224320
8	BCL3	chr5:97224086-97224486	GM12878	blood:	n/a	chr5:97224311-97224320
9	BHLHE40	chr5:97224143-97224411	GM12878	blood:	n/a	n/a
10	BRCA1	chr5:97205114-97205124	GM12878	blood:	n/a	n/a
11	CEBPB	chr5:97324370-97324626	HepG2	liver:	n/a	chr5:97324472-97324483
12	CEBPB	chr5:97227989-97228292	HepG2	liver:	n/a	chr5:97228176-97228188 chr5:97228138-97228151 chr5:97228138-97228151 chr5:97228138-97228149 chr5:97228139-97228150
13	CEBPB	chr5:97315569-97315781	IMR90	lung:	n/a	n/a
14	CEBPB	chr5:97205605-97205797	IMR90	lung:	n/a	chr5:97205715-97205726
15	CEBPB	chr5:97324361-97324490	H1-hESC	embryonic stem cell:	n/a	chr5:97324472-97324483
16	CEBPB	chr5:97256659-97256920	HepG2	liver:	n/a	n/a
17	CEBPB	chr5:97252072-97252272	A549	lung:	n/a	chr5:97252182-97252193
18	CEBPB	chr5:97227985-97228252	IMR90	lung:	n/a	chr5:97228176-97228188 chr5:97228138-97228151 chr5:97228138-97228151 chr5:97228138-97228149 chr5:97228139-97228150
19	CEBPB	chr5:97252040-97252324	HepG2	liver:	n/a	chr5:97252182-97252193
20	CEBPB	chr5:97252023-97252330	IMR90	lung:	n/a	chr5:97252182-97252193
21	CEBPB	chr5:97288323-97288547	HepG2	liver:	n/a	chr5:97288387-97288400 chr5:97288387-97288400 chr5:97288519-97288532
22	CEBPB	chr5:97325294-97325607	IMR90	lung:	n/a	n/a
23	CEBPB	chr5:97202094-97202237	IMR90	lung:	n/a	n/a
24	CEBPB	chr5:97324575-97324602	A549	lung:	n/a	n/a
25	CEBPB	chr5:97205594-97205877	HepG2	liver:	n/a	chr5:97205715-97205726
26	CHD2	chr5:97259772-97260470	GM12878	blood:	n/a	n/a
27	CTCF	chr5:97321940-97322090	GM12874	blood:	n/a	chr5:97322002-97322018 chr5:97321996-97322017 chr5:97322001-97322019
28	CTCF	chr5:97321920-97322070	HCPEpiC	choroid plexus:	n/a	chr5:97322002-97322018 chr5:97321996-97322017 chr5:97322001-97322019
29	CTCF	chr5:97321900-97322050	HA-sp	spinal cord:	n/a	chr5:97322002-97322018 chr5:97321996-97322017 chr5:97322001-97322019
30	CTCF	chr5:97321960-97322110	HA-sp	spinal cord:	n/a	chr5:97322002-97322018 chr5:97321996-97322017 chr5:97322001-97322019
31	CTCF	chr5:97213320-97213470	MCF-7	breast:	n/a	n/a
32	CTCF	chr5:97322020-97322170	HFF	foreskin:	n/a	n/a
33	CTCF	chr5:97213420-97213570	MCF-7	breast:	n/a	n/a
34	CTCF	chr5:97253934-97254010	GM20000	blood:	n/a	n/a
35	CTCF	chr5:97321869-97322189	GM12878	blood:	n/a	chr5:97322002-97322018 chr5:97321996-97322017 chr5:97322001-97322019
36	CTCF	chr5:97321948-97321996	GM19238	blood:	n/a	n/a
37	CTCF	chr5:97290420-97290570	NHEK	skin:	n/a	n/a
38	CTCF	chr5:97321920-97322070	HFF-Myc	foreskin:	n/a	chr5:97322002-97322018 chr5:97321996-97322017 chr5:97322001-97322019
39	CTCF	chr5:97321898-97322101	MCF-7	breast:	n/a	chr5:97322002-97322018 chr5:97321996-97322017 chr5:97322001-97322019
40	CTCF	chr5:97321940-97322090	AG10803	skin:	n/a	chr5:97322002-97322018 chr5:97321996-97322017 chr5:97322001-97322019
41	CTCF	chr5:97321940-97322090	AG09309	skin:	n/a	chr5:97322002-97322018 chr5:97321996-97322017 chr5:97322001-97322019
42	CTCF	chr5:97321954-97322068	LNCaP	prostate:	n/a	chr5:97322002-97322018 chr5:97321996-97322017 chr5:97322001-97322019
43	CTCF	chr5:97213380-97213530	HBMEC	blood vessel:	n/a	n/a
44	CTCF	chr5:97321921-97322114	Gliobla	brain:	n/a	chr5:97322002-97322018 chr5:97321996-97322017 chr5:97322001-97322019
45	CTCF	chr5:97321951-97322073	LNCaP	prostate:	n/a	chr5:97322002-97322018 chr5:97321996-97322017 chr5:97322001-97322019
46	CTCF	chr5:97321980-97322130	AG10803	skin:	n/a	chr5:97322002-97322018 chr5:97321996-97322017 chr5:97322001-97322019
47	CTCF	chr5:97321900-97322050	HCPEpiC	choroid plexus:	n/a	chr5:97322002-97322018 chr5:97321996-97322017 chr5:97322001-97322019
48	CTCF	chr5:97213445-97213511	GM19238	blood:	n/a	n/a
49	CTCF	chr5:97321860-97322010	GM12874	blood:	n/a	n/a
50	CTCF	chr5:97321962-97322037	GM19239	blood:	n/a	chr5:97322002-97322018 chr5:97321996-97322017 chr5:97322001-97322019

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:97315689-97315739	HCM	heart:	n/a
2	chr5:97315689-97315739	Jurkat	blood:	n/a
3	chr5:97315689-97315739	HAEpiC	amniotic membrane:	n/a
4	chr5:97191292-97191342	NHBE	bronchial:	n/a
5	chr5:97191292-97191342	Hepatocyte	liver:	n/a
6	chr5:97315689-97315739	LNCaP	prostate:	n/a
7	chr5:97315689-97315739	HRE	kidney:	n/a
8	chr5:97315689-97315739	HRPEpiC	eye:	n/a
9	chr5:97315689-97315739	NH-A	brain:	n/a
10	chr5:97315689-97315739	HCT-116	colon:	n/a
11	chr5:97315689-97315739	PFSK-1	brain:	n/a
12	chr5:97315689-97315739	NB4	blood:	n/a
13	chr5:97315689-97315739	AoSMC	blood vessel:	n/a
14	chr5:97191292-97191342	GM06990	blood:	n/a
15	chr5:97191292-97191342	A549	lung:	n/a
16	chr5:97191292-97191342	Jurkat	blood:	n/a
17	chr5:97191292-97191342	AG10803	skin:	n/a
18	chr5:97191292-97191342	PrEC	prostate:	n/a
19	chr5:97191292-97191342	AG04450	lung:	fetal
20	chr5:97191292-97191342	ovcar-3	ovarian:	n/a
21	chr5:97315689-97315739	GM19239	blood:	n/a
22	chr5:97315689-97315739	SK-N-SH_RA	brain:	n/a
23	chr5:97191292-97191342	NHDF-neo	bronchial:	n/a
24	chr5:97315689-97315739	ovcar-3	ovarian:	n/a
25	chr5:97191292-97191342	HIPEpiC	eye:	n/a
26	chr5:97191292-97191342	HMEC	breast:	n/a
27	chr5:97191292-97191342	BE2_C	brain:	n/a
28	chr5:97315689-97315739	HRCEpiC	kidney:	n/a
29	chr5:97315689-97315739	BJ	skin:	n/a
30	chr5:97315689-97315739	AG09309	skin:	n/a
31	chr5:97191292-97191342	AG04449	skin:	fetal
32	chr5:97315689-97315739	ECC-1	luminal epithelium:	n/a
33	chr5:97191292-97191342	ECC-1	luminal epithelium:	n/a
34	chr5:97191292-97191342	SK-N-SH_RA	brain:	n/a
35	chr5:97315689-97315739	HPAEpiC	pulmonary alveolar:	n/a
36	chr5:97191292-97191342	HUVEC	blood vessel:	n/a
37	chr5:97315689-97315739	MCF-7	breast:	n/a
38	chr5:97315689-97315739	HMEC	breast:	n/a
39	chr5:97191292-97191342	H1-hESC	embryonic stem cell:	embryo
40	chr5:97315689-97315739	K562	blood:	n/a
41	chr5:97191292-97191342	HPAEpiC	pulmonary alveolar:	n/a
42	chr5:97315689-97315739	MCF10A-Er-Src	breast:	n/a
43	chr5:97315689-97315739	CMK	blood:	n/a
44	chr5:97315689-97315739	ProgFib	skin:	n/a
45	chr5:97315689-97315739	U87	brain:	n/a
46	chr5:97191292-97191342	PANC-1	pancreas:	n/a
47	chr5:97315689-97315739	HCF	heart:	n/a
48	chr5:97191292-97191342	HepG2	liver:	n/a
49	chr5:97191292-97191342	HAEpiC	amniotic membrane:	n/a
50	chr5:97315689-97315739	PrEC	prostate:	n/a

No.	Distal block	Cell Line	Cell type
1	chr5:97207148..97208975-chr5:97213192..97214894,2	K562	blood:
2	chr5:97207148..97208975-chr5:97213192..97214894,2	K562	blood:
3	chr5:97203818..97206757-chr5:97208812..97211809,2	K562	blood:
4	chr5:97203818..97206757-chr5:97208812..97211809,2	K562	blood:
5	chr5:96987103..96987619-chr5:97253568..97254119,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CTD-2215E18.1.1-3	chr5:97217124-97217271	XLOC_004484
2	lnc-CTD-2215E18.1.1-3	chr5:97235342-97235457	XLOC_004484
3	lnc-CTD-2215E18.1.1-3	chr5:97217132-97217271	XLOC_004484
4	lnc-CTD-2215E18.1.1-3	chr5:97257835-97258399	XLOC_004484

Variant related genes	Relation type
ENSG00000248202	TF binding region
ENSG00000248202	CpG island
DNAJB12	miRNA target sites

Extended variants
information (count: 2107 )
Associated
traits (count: 82 )

Variant overlapped rSNPs/rCNVs (count:2107 , 50 per page) page: 1 2 3 4 5 6 7 ... 43

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs566601733	chr5:97190960-97190961	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
2	rs566219670	chr5:97190985-97190986	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs374905246	chr5:97190999-97191000	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs376454146	chr5:97191007-97191008	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs552217443	chr5:97191009-97191010	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs141595894	chr5:97191024-97191025	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs537819779	chr5:97191030-97191031	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs144274372	chr5:97191053-97191054	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs556532811	chr5:97191095-97191096	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs116780851	chr5:97191122-97191123	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs529722063	chr5:97191132-97191133	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs535693110	chr5:97191138-97191139	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs553693353	chr5:97191140-97191141	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs7729626	chr5:97191178-97191179	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs546002838	chr5:97191210-97191211	Enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs557806354	chr5:97191227-97191228	Enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs148391226	chr5:97191239-97191240	Enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs566054766	chr5:97191244-97191245	Enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs72781511	chr5:97191256-97191257	Enhancers Strong transcription Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs528809948	chr5:97191267-97191268	Enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs192988006	chr5:97191292-97191293	Enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs142743324	chr5:97191354-97191355	Enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs367773635	chr5:97191360-97191361	Enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs150587003	chr5:97191391-97191392	Enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs538729195	chr5:97191422-97191423	Strong transcription Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs72781512	chr5:97191431-97191432	Strong transcription Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs4419613	chr5:97191470-97191471	Strong transcription Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs570546755	chr5:97191541-97191542	Strong transcription Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs4419614	chr5:97191567-97191568	Strong transcription Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs549800263	chr5:97191660-97191661	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs568018319	chr5:97191710-97191711	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs535398881	chr5:97191739-97191740	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs139588453	chr5:97191747-97191748	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs144387788	chr5:97191780-97191781	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs550665469	chr5:97191793-97191794	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs567384001	chr5:97191820-97191821	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs147816993	chr5:97191864-97191865	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs539600859	chr5:97191877-97191878	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs185233332	chr5:97191954-97191955	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs570500381	chr5:97191955-97191956	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs199759797	chr5:97191992-97191993	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs386690319	chr5:97191995-97191996	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs72781514	chr5:97191997-97191998	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs555352320	chr5:97192017-97192018	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs72781515	chr5:97192044-97192045	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs541385131	chr5:97192049-97192050	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs559975637	chr5:97192084-97192085	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs188900496	chr5:97192097-97192098	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs201089734	chr5:97192153-97192154	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs193226046	chr5:97192197-97192198	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:82)

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
Breast cancer	21611746	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Glioblastoma multiforme	22286061	CNVD

Chromatin state (count:136 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:97187000-97196800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr5:97190000-97192600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
3	chr5:97190200-97191200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
4	chr5:97190200-97191200	Flanking Active TSS	Adipose Nuclei	Adipose
5	chr5:97190200-97191400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
6	chr5:97190200-97191400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
7	chr5:97190200-97191400	Enhancers	NHLF	lung
8	chr5:97190400-97191000	Enhancers	ES-WA7 Cell Line	embryonic stem cell
9	chr5:97190400-97191200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
10	chr5:97190400-97191200	Enhancers	Placenta Amnion	Placenta Amnion
11	chr5:97190400-97191400	Enhancers	Fetal Muscle Trunk	muscle
12	chr5:97190600-97191000	Enhancers	NH-A	brain
13	chr5:97190600-97191600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
14	chr5:97190800-97191200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
15	chr5:97191200-97191600	Strong transcription	iPS DF 19.11 Cell Line	embryonic stem cell
16	chr5:97191600-97193200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
17	chr5:97209800-97210000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
18	chr5:97210000-97210400	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
19	chr5:97210000-97210400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
20	chr5:97210000-97210600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
21	chr5:97210000-97210600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
22	chr5:97210000-97210800	Enhancers	Muscle Satellite Cultured Cells	--
23	chr5:97210000-97210800	Enhancers	NHDF-Ad	bronchial
24	chr5:97210200-97210600	Enhancers	HSMMtube	muscle
25	chr5:97210400-97210800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
26	chr5:97210800-97212800	Weak transcription	NHDF-Ad	bronchial
27	chr5:97210800-97213800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
28	chr5:97211400-97211800	Enhancers	Gastric	stomach
29	chr5:97211600-97212400	Enhancers	Stomach Mucosa	stomach
30	chr5:97212600-97213000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
31	chr5:97212800-97213600	Enhancers	NHDF-Ad	bronchial
32	chr5:97213200-97214000	Enhancers	Brain Inferior Temporal Lobe	brain
33	chr5:97213400-97213800	Enhancers	Adipose Nuclei	Adipose
34	chr5:97213600-97213800	Enhancers	Brain Substantia Nigra	brain
35	chr5:97213600-97214000	Enhancers	Brain Anterior Caudate	brain
36	chr5:97213600-97214000	Enhancers	Brain Hippocampus Middle	brain
37	chr5:97214400-97214800	Enhancers	Brain Germinal Matrix	brain
38	chr5:97215000-97215600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
39	chr5:97217600-97218200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
40	chr5:97224200-97224800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
41	chr5:97224200-97224800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
42	chr5:97235200-97238200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
43	chr5:97238200-97239000	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
44	chr5:97238600-97239000	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
45	chr5:97239600-97240800	ZNF genes & repeats	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
46	chr5:97240200-97240800	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
47	chr5:97240800-97245200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
48	chr5:97241400-97243400	Enhancers	iPS-15b Cell Line	embryonic stem cell
49	chr5:97241600-97241800	Enhancers	HUES48 Cell Line	embryonic stem cell
50	chr5:97241600-97241800	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell

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