Variant report

Variant	nsv964930
Chromosome Location	chr5:118301974-118317943
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:127)
CpG islands
(count:428)
Chromatin interactive
region (count:7)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:127 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BATF	chr5:118309656-118309802	GM12878	blood:	n/a	n/a
2	BCL11A	chr5:118309390-118309588	GM12878	blood:	n/a	n/a
3	BCL11A	chr5:118309262-118309620	GM12878	blood:	n/a	n/a
4	BCL11A	chr5:118309651-118309813	GM12878	blood:	n/a	n/a
5	CEBPB	chr5:118302496-118303264	MCF-7	breast:	n/a	n/a
6	CTCF	chr5:118315414-118315479	GM13976	blood:	n/a	n/a
7	CTCF	chr5:118312700-118312850	A549	lung:	n/a	n/a
8	E2F4	chr5:118317544-118317842	MCF10A-Er-Src	breast:	n/a	n/a
9	E2F6	chr5:118304213-118304722	H1-hESC	embryonic stem cell:	n/a	n/a
10	EBF1	chr5:118309757-118310098	GM12878	blood:	n/a	n/a
11	EBF1	chr5:118309724-118310058	GM12878	blood:	n/a	n/a
12	EGR1	chr5:118302803-118303199	MCF-7	breast:	n/a	n/a
13	ELF1	chr5:118302734-118303352	MCF-7	breast:	n/a	n/a
14	EP300	chr5:118304285-118304335	HepG2	liver:	n/a	n/a
15	EP300	chr5:118309593-118309822	GM12878	blood:	n/a	n/a
16	FOS	chr5:118317515-118317867	MCF10A-Er-Src	breast:	n/a	n/a
17	FOS	chr5:118317515-118317890	MCF10A-Er-Src	breast:	n/a	n/a
18	FOS	chr5:118317517-118317867	MCF10A-Er-Src	breast:	n/a	n/a
19	FOS	chr5:118317532-118317869	MCF10A-Er-Src	breast:	n/a	n/a
20	FOSL2	chr5:118309258-118309519	HepG2	liver:	n/a	n/a
21	GATA2	chr5:118309383-118309693	K562	blood:	n/a	n/a
22	GATA3	chr5:118302759-118303225	T-47D	breast:	n/a	n/a
23	GATA3	chr5:118302755-118303248	MCF-7	breast:	n/a	n/a
24	GATA3	chr5:118302398-118303490	MCF-7	breast:	n/a	n/a
25	GATA3	chr5:118302574-118303364	MCF-7	breast:	n/a	n/a
26	GATA3	chr5:118302794-118303299	MCF-7	breast:	n/a	n/a
27	GATA3	chr5:118302881-118303296	T-47D	breast:	n/a	n/a
28	HDAC2	chr5:118302832-118303212	MCF-7	breast:	n/a	n/a
29	HDAC2	chr5:118302599-118303378	MCF-7	breast:	n/a	n/a
30	HEY1	chr5:118309173-118309643	HepG2	liver:	n/a	n/a
31	HEY1	chr5:118310080-118310543	K562	blood:	n/a	n/a
32	HEY1	chr5:118309191-118309618	K562	blood:	n/a	n/a
33	HEY1	chr5:118309209-118309537	HepG2	liver:	n/a	n/a
34	HEY1	chr5:118309179-118310062	K562	blood:	n/a	n/a
35	HEY1	chr5:118310164-118310476	HepG2	liver:	n/a	n/a
36	IRF1	chr5:118316258-118316270	K562	blood:	n/a	n/a
37	KAP1	chr5:118302508-118303214	U2OS	brain:	n/a	n/a
38	KAP1	chr5:118302579-118303340	HEK293	kidney:	n/a	n/a
39	MAFF	chr5:118316090-118316417	HepG2	liver:	n/a	chr5:118316266-118316284
40	MAFK	chr5:118314025-118314111	HepG2	liver:	n/a	n/a
41	MAFK	chr5:118316155-118316439	HepG2	liver:	n/a	chr5:118316267-118316282
42	MAFK	chr5:118316139-118316388	IMR90	lung:	n/a	chr5:118316267-118316282
43	MAFK	chr5:118316102-118316429	HepG2	liver:	n/a	chr5:118316267-118316282
44	MAX	chr5:118304372-118304412	HepG2	liver:	n/a	n/a
45	MYC	chr5:118317517-118317773	MCF10A-Er-Src	breast:	n/a	n/a
46	MYC	chr5:118317458-118317741	MCF10A-Er-Src	breast:	n/a	n/a
47	NR2F2	chr5:118302395-118303379	MCF-7	breast:	n/a	n/a
48	NR2F2	chr5:118302705-118303363	MCF-7	breast:	n/a	n/a
49	PAX5	chr5:118309705-118310044	GM12878	blood:	n/a	n/a
50	PBX3	chr5:118309337-118309470	GM12878	blood:	n/a	n/a

(count:428 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:118309333-118309383	HepG2	liver:	n/a
2	chr5:118309333-118309383	HepG2	liver:	n/a
3	chr5:118309460-118309510	RPTEC	kidney:	n/a
4	chr5:118312966-118313016	HEEpiC	esophagus:	n/a
5	chr5:118309902-118309952	ProgFib	skin:	n/a
6	chr5:118312966-118313016	A549	lung:	n/a
7	chr5:118309333-118309383	SK-N-SH	brain:	n/a
8	chr5:118308850-118308900	T-47D	breast:	n/a
9	chr5:118309333-118309383	CMK	blood:	n/a
10	chr5:118309902-118309952	HRE	kidney:	n/a
11	chr5:118309460-118309510	K562	blood:	n/a
12	chr5:118312966-118313016	T-47D	breast:	n/a
13	chr5:118309902-118309952	Jurkat	blood:	n/a
14	chr5:118309460-118309510	SAEC	small airway:	n/a
15	chr5:118312966-118313016	AG09309	skin:	n/a
16	chr5:118309902-118309952	HL-60	blood:	n/a
17	chr5:118308850-118308900	HCM	heart:	n/a
18	chr5:118309902-118309952	HCM	heart:	n/a
19	chr5:118308850-118308900	HUVEC	blood vessel:	n/a
20	chr5:118306150-118306200	T-47D	breast:	n/a
21	chr5:118308850-118308900	NT2-D1	testis:	n/a
22	chr5:118312966-118313016	MCF10A-Er-Src	breast:	n/a
23	chr5:118306150-118306200	PANC-1	pancreas:	n/a
24	chr5:118309939-118309989	T-47D	breast:	n/a
25	chr5:118309333-118309383	AG04449	skin:	fetal
26	chr5:118306150-118306200	AG04450	lung:	fetal
27	chr5:118306150-118306200	HL-60	blood:	n/a
28	chr5:118308850-118308900	AG04450	lung:	fetal
29	chr5:118309460-118309510	PFSK-1	brain:	n/a
30	chr5:118309333-118309383	HEEpiC	esophagus:	n/a
31	chr5:118309939-118309989	HUVEC	blood vessel:	n/a
32	chr5:118312966-118313016	GM06990	blood:	n/a
33	chr5:118309939-118309989	HCPEpiC	choroid plexus:	n/a
34	chr5:118309460-118309510	HL-60	blood:	n/a
35	chr5:118309333-118309383	Hepatocyte	liver:	n/a
36	chr5:118309939-118309989	HCF	heart:	n/a
37	chr5:118309460-118309510	PrEC	prostate:	n/a
38	chr5:118306150-118306200	GM12892	blood:	n/a
39	chr5:118312966-118313016	HAEpiC	amniotic membrane:	n/a
40	chr5:118312966-118313016	NT2-D1	testis:	n/a
41	chr5:118309460-118309510	IMR90	lung:	fetal
42	chr5:118309939-118309989	NT2-D1	testis:	n/a
43	chr5:118308850-118308900	HNPCEpiC	eye:	n/a
44	chr5:118309939-118309989	MCF-7	breast:	n/a
45	chr5:118309939-118309989	AoSMC	blood vessel:	n/a
46	chr5:118309460-118309510	U87	brain:	n/a
47	chr5:118309460-118309510	NHBE	bronchial:	n/a
48	chr5:118312966-118313016	HL-60	blood:	n/a
49	chr5:118312966-118313016	SKMC	muscle:	n/a
50	chr5:118312966-118313016	Caco-2	colon:	n/a

(count:7 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr5:118315933..118319835-chr5:118323303..118326680,3	MCF-7	breast:
2	chr5:118311467..118314093-chr5:118314485..118317147,2	K562	blood:
3	chr5:118302817..118305365-chr5:118322521..118324091,2	MCF-7	breast:
4	chr5:118311467..118314093-chr5:118314485..118317147,2	K562	blood:
5	chr5:118315876..118318901-chr5:118321943..118324259,3	MCF-7	breast:
6	chr5:118315792..118320529-chr5:118321733..118325729,5	K562	blood:
7	chr5:118302138..118305564-chr5:118322264..118325147,4	K562	blood:

No data

Variant related genes	Relation type
PTMAP2	TF binding region
PTMAP2	CpG island
ENSG00000169570	chromatin interactions

Extended variants
information (count: 718 )
Associated
traits (count: 73 )

Variant overlapped rSNPs/rCNVs (count:718 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs575173279	chr5:118301987-118301988	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs558492504	chr5:118301989-118301990	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs151191117	chr5:118302015-118302016	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs577925144	chr5:118302020-118302021	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs187274294	chr5:118302023-118302024	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs560365960	chr5:118302035-118302036	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs573417464	chr5:118302054-118302055	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs10463707	chr5:118302142-118302143	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs561944406	chr5:118302147-118302148	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs535115956	chr5:118302149-118302150	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs534429078	chr5:118302200-118302201	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs74641087	chr5:118302239-118302240	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs571900281	chr5:118302250-118302251	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs542446955	chr5:118302254-118302255	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs140323100	chr5:118302265-118302266	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs115002919	chr5:118302300-118302301	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs561014822	chr5:118302311-118302312	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs533424824	chr5:118302327-118302328	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs557106875	chr5:118302343-118302344	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs75744913	chr5:118302355-118302356	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs192064648	chr5:118302356-118302357	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs535242387	chr5:118302394-118302395	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs549016137	chr5:118302450-118302451	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs568769521	chr5:118302494-118302495	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs537811113	chr5:118302507-118302508	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs299200	chr5:118302517-118302518	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs112258616	chr5:118302523-118302524	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs554058143	chr5:118302524-118302525	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs573735434	chr5:118302553-118302554	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs113052643	chr5:118302554-118302555	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs145767444	chr5:118302561-118302562	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs575571927	chr5:118302570-118302571	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs6872295	chr5:118302585-118302586	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs183414210	chr5:118302587-118302588	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs533487950	chr5:118302588-118302589	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs187420032	chr5:118302659-118302660	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs6872652	chr5:118302677-118302678	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs146961885	chr5:118302678-118302679	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs148343182	chr5:118302689-118302690	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs73240707	chr5:118302696-118302697	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs373997522	chr5:118302738-118302739	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs113213191	chr5:118302752-118302753	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs537522148	chr5:118302757-118302758	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs77035042	chr5:118302765-118302766	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs79458658	chr5:118302766-118302767	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs551428900	chr5:118302779-118302780	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs571262044	chr5:118302793-118302794	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs141522154	chr5:118302847-118302848	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs534084069	chr5:118302867-118302868	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs190646210	chr5:118302897-118302898	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:73)

Disease	PMID	Source
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
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
Bipolar disorder	18458673	CNVD
Thyroid cancer	19087340	CNVD
Breast cancer	21785460	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
Cancer	20164920	CNVD
Myelodysplastic syndrome	21251322	CNVD
Colorectal cancer	16272173	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Multiple myeloma	17550852	CNVD
Ovarian cancer	21720365	CNVD
Salivary gland tumor	18059337	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Renal cell carcinoma	19377443	CNVD
Prostate cancer	16461572	CNVD
Myelofibrosis	22110671	CNVD
Esophageal squamous carcinoma	17470683	CNVD
Glaucoma	21310917	CNVD
Glioblastoma multiforme	22286061	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Prostate cancer	22341455	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:120 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:118259600-118305000	Weak transcription	Stomach Smooth Muscle	stomach
2	chr5:118263000-118306000	Weak transcription	Primary T cells from cord blood	blood
3	chr5:118263400-118304000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
4	chr5:118282200-118304200	Weak transcription	Right Atrium	heart
5	chr5:118294400-118304200	Weak transcription	Left Ventricle	heart
6	chr5:118296800-118314400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
7	chr5:118299400-118304600	Weak transcription	Skeletal Muscle Female	skeletal muscle
8	chr5:118299800-118304200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
9	chr5:118301000-118304200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
10	chr5:118301200-118304000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
11	chr5:118301800-118304000	Enhancers	Hela-S3	cervix
12	chr5:118302600-118302800	Enhancers	Pancreas	Pancrea
13	chr5:118302600-118304000	Enhancers	HepG2	liver
14	chr5:118302600-118304200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
15	chr5:118302800-118305000	Weak transcription	Pancreas	Pancrea
16	chr5:118303000-118303200	Enhancers	K562	blood
17	chr5:118303400-118304000	Weak transcription	K562	blood
18	chr5:118304000-118304200	Enhancers	Primary T helper naive cells from peripheral blood	blood
19	chr5:118304000-118304200	Enhancers	K562	blood
20	chr5:118304000-118304400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
21	chr5:118304000-118304400	Enhancers	Primary B cells from peripheral blood	blood
22	chr5:118304000-118304400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
23	chr5:118304000-118304400	Enhancers	Primary T helper cells PMA-I stimulated	--
24	chr5:118304000-118304600	Enhancers	Primary T helper naive cells fromperipheralblood	blood
25	chr5:118304000-118304800	Weak transcription	Hela-S3	cervix
26	chr5:118304000-118305400	Enhancers	HUES6 Cell Line	embryonic stem cell
27	chr5:118304000-118305400	Flanking Active TSS	HepG2	liver
28	chr5:118304200-118304400	Enhancers	Right Atrium	heart
29	chr5:118304200-118304600	Enhancers	Primary T cells fromperipheralblood	blood
30	chr5:118304200-118304800	Weak transcription	K562	blood
31	chr5:118304200-118305000	Strong transcription	Foreskin Melanocyte Primary Cells skin01	Skin
32	chr5:118304200-118305200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
33	chr5:118304200-118305200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
34	chr5:118304200-118305200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
35	chr5:118304200-118305200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
36	chr5:118304200-118305200	Enhancers	Left Ventricle	heart
37	chr5:118304200-118305400	Enhancers	Right Ventricle	heart
38	chr5:118304400-118304600	Flanking Active TSS	Primary B cells from peripheral blood	blood
39	chr5:118304400-118304800	Enhancers	H1 Cell Line	embryonic stem cell
40	chr5:118304400-118304800	Weak transcription	Right Atrium	heart
41	chr5:118304400-118305200	Enhancers	Fetal Muscle Trunk	muscle
42	chr5:118304400-118305400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
43	chr5:118304400-118305400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
44	chr5:118304400-118305400	Enhancers	Adipose Nuclei	Adipose
45	chr5:118304400-118311200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
46	chr5:118304600-118304800	ZNF genes & repeats	Fetal Stomach	stomach
47	chr5:118304600-118305400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
48	chr5:118304600-118305400	Enhancers	Fetal Muscle Leg	muscle
49	chr5:118304600-118305400	Enhancers	Skeletal Muscle Female	skeletal muscle
50	chr5:118304600-118321600	Weak transcription	Primary T helper naive cells fromperipheralblood	blood

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