Variant report

Variant	nsv599489
Chromosome Location	chr5:117042759-117120444
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:185)
CpG islands
(count:123)
Chromatin interactive
region (count:9)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:185 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CBX3	chr5:117049291-117049655	K562	blood:	n/a	n/a
2	CBX3	chr5:117049184-117049819	HCT-116	colon:	n/a	n/a
3	CBX3	chr5:117049274-117049666	K562	blood:	n/a	n/a
4	CBX3	chr5:117049153-117049707	HCT-116	colon:	n/a	n/a
5	CEBPB	chr5:117067971-117068479	ECC-1	luminal epithelium:	n/a	n/a
6	CEBPZ	chr5:117049337-117049629	HepG2	liver:	n/a	n/a
7	CTCF	chr5:117070660-117070810	AG09319	gingival:	n/a	n/a
8	CTCF	chr5:117070660-117070810	HPAF	blood vessel:	n/a	n/a
9	CTCF	chr5:117103172-117103228	K562	blood:	n/a	n/a
10	CTCF	chr5:117070620-117070770	AG04449	skin:	n/a	n/a
11	CTCF	chr5:117109043-117109065	MCF-7	breast:	n/a	n/a
12	CTCF	chr5:117071892-117071897	GM12878	blood:	n/a	n/a
13	CTCF	chr5:117070720-117070870	NHDF-neo	bronchial:	n/a	n/a
14	CTCF	chr5:117070600-117070750	HPF	lung:	n/a	n/a
15	CTCF	chr5:117105540-117105630	GM13976	blood:	n/a	n/a
16	CTCF	chr5:117070580-117070730	NHDF-neo	bronchial:	n/a	n/a
17	CTCF	chr5:117070640-117070790	HPAF	blood vessel:	n/a	n/a
18	CTCF	chr5:117070740-117070890	MCF-7	breast:	n/a	n/a
19	CTCF	chr5:117068480-117068630	Caco-2	colon:	n/a	n/a
20	CTCF	chr5:117070760-117070910	HEK293	kidney:	n/a	n/a
21	CTCF	chr5:117070620-117070770	AG09319	gingival:	n/a	n/a
22	CTCF	chr5:117070640-117070790	BJ	skin:	n/a	n/a
23	CTCF	chr5:117070620-117070770	SK-N-SH_RA	brain:	n/a	n/a
24	CTCF	chr5:117070540-117070690	WI-38	lung:	n/a	n/a
25	CTCF	chr5:117049440-117049590	NHEK	skin:	n/a	n/a
26	E2F4	chr5:117066785-117067006	MCF10A-Er-Src	breast:	n/a	n/a
27	E2F4	chr5:117069844-117070117	MCF10A-Er-Src	breast:	n/a	n/a
28	E2F4	chr5:117049850-117050028	MCF10A-Er-Src	breast:	n/a	n/a
29	E2F4	chr5:117085588-117085772	MCF10A-Er-Src	breast:	n/a	n/a
30	E2F4	chr5:117043607-117043713	MCF10A-Er-Src	breast:	n/a	n/a
31	EBF1	chr5:117069780-117069874	GM12878	blood:	n/a	n/a
32	ELF1	chr5:117049201-117049754	HCT-116	colon:	n/a	n/a
33	EP300	chr5:117067081-117067620	ECC-1	luminal epithelium:	n/a	chr5:117067371-117067381
34	EP300	chr5:117112787-117112865	GM12878	blood:	n/a	n/a
35	EP300	chr5:117049312-117049533	SK-N-SH_RA	brain:	n/a	n/a
36	EP300	chr5:117084083-117084410	H1-hESC	embryonic stem cell:	n/a	n/a
37	EP300	chr5:117049313-117049626	ECC-1	luminal epithelium:	n/a	n/a
38	EP300	chr5:117049218-117049689	ECC-1	luminal epithelium:	n/a	n/a
39	EP300	chr5:117049356-117049650	K562	blood:	n/a	n/a
40	EP300	chr5:117067754-117068606	ECC-1	luminal epithelium:	n/a	n/a
41	EP300	chr5:117049410-117049602	GM12878	blood:	n/a	n/a
42	FOS	chr5:117049389-117049401	MCF10A-Er-Src	breast:	n/a	n/a
43	FOSL2	chr5:117108967-117109179	HepG2	liver:	n/a	n/a
44	FOXA1	chr5:117097409-117097872	HepG2	liver:	n/a	chr5:117097627-117097639
45	FOXA1	chr5:117067205-117067487	ECC-1	luminal epithelium:	n/a	chr5:117067366-117067381 chr5:117067368-117067380
46	FOXA1	chr5:117067125-117067515	ECC-1	luminal epithelium:	n/a	chr5:117067366-117067381 chr5:117067368-117067380
47	FOXA1	chr5:117067259-117067490	T-47D	breast:	n/a	chr5:117067366-117067381 chr5:117067368-117067380
48	FOXA1	chr5:117097521-117097739	HepG2	liver:	n/a	chr5:117097627-117097639
49	FOXA1	chr5:117077605-117077799	T-47D	breast:	n/a	n/a
50	FOXM1	chr5:117067842-117068587	ECC-1	luminal epithelium:	n/a	n/a

(count:123 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:117098484-117098534	U87	brain:	n/a
2	chr5:117098484-117098534	U87	brain:	n/a
3	chr5:117084231-117084281	HepG2	liver:	n/a
4	chr5:117084231-117084281	HCF	heart:	n/a
5	chr5:117098484-117098534	PFSK-1	brain:	n/a
6	chr5:117098484-117098534	GM12892	blood:	n/a
7	chr5:117084231-117084281	NB4	blood:	n/a
8	chr5:117084231-117084281	AG09319	gingival:	n/a
9	chr5:117084231-117084281	NT2-D1	testis:	n/a
10	chr5:117084231-117084281	MCF10A-Er-Src	breast:	n/a
11	chr5:117098484-117098534	AoSMC	blood vessel:	n/a
12	chr5:117084231-117084281	CMK	blood:	n/a
13	chr5:117084231-117084281	AoSMC	blood vessel:	n/a
14	chr5:117084231-117084281	K562	blood:	n/a
15	chr5:117098484-117098534	LNCaP	prostate:	n/a
16	chr5:117084231-117084281	SK-N-MC	brain:	n/a
17	chr5:117098484-117098534	SK-N-SH	brain:	n/a
18	chr5:117084231-117084281	LNCaP	prostate:	n/a
19	chr5:117084231-117084281	MCF-7	breast:	n/a
20	chr5:117084231-117084281	AG04449	skin:	fetal
21	chr5:117098484-117098534	Caco-2	colon:	n/a
22	chr5:117084231-117084281	PFSK-1	brain:	n/a
23	chr5:117084231-117084281	Hela-S3	cervix:	n/a
24	chr5:117084231-117084281	AG09309	skin:	n/a
25	chr5:117098484-117098534	MCF10A-Er-Src	breast:	n/a
26	chr5:117098484-117098534	IMR90	lung:	fetal
27	chr5:117084231-117084281	Hepatocyte	liver:	n/a
28	chr5:117084231-117084281	GM19239	blood:	n/a
29	chr5:117084231-117084281	PANC-1	pancreas:	n/a
30	chr5:117084231-117084281	BJ	skin:	n/a
31	chr5:117084231-117084281	GM12892	blood:	n/a
32	chr5:117098484-117098534	HCM	heart:	n/a
33	chr5:117084231-117084281	HAEpiC	amniotic membrane:	n/a
34	chr5:117084231-117084281	NH-A	brain:	n/a
35	chr5:117084231-117084281	SAEC	small airway:	n/a
36	chr5:117098484-117098534	NHDF-neo	bronchial:	n/a
37	chr5:117084231-117084281	HMEC	breast:	n/a
38	chr5:117084231-117084281	HCPEpiC	choroid plexus:	n/a
39	chr5:117098484-117098534	HL-60	blood:	n/a
40	chr5:117098484-117098534	SKMC	muscle:	n/a
41	chr5:117098484-117098534	HCT-116	colon:	n/a
42	chr5:117084231-117084281	HCT-116	colon:	n/a
43	chr5:117098484-117098534	HEEpiC	esophagus:	n/a
44	chr5:117084231-117084281	HEEpiC	esophagus:	n/a
45	chr5:117098484-117098534	Jurkat	blood:	n/a
46	chr5:117084231-117084281	SK-N-SH	brain:	n/a
47	chr5:117098484-117098534	HUVEC	blood vessel:	n/a
48	chr5:117098484-117098534	AG09319	gingival:	n/a
49	chr5:117098484-117098534	PrEC	prostate:	n/a
50	chr5:117098484-117098534	MCF-7	breast:	n/a

(count:9 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr5:117089885..117092759-chr5:117093000..117095939,2	MCF-7	breast:
2	chr5:117072184..117074866-chr5:118040239..118042048,2	MCF-7	breast:
3	chr5:117050991..117053069-chr5:117068100..117070459,2	MCF-7	breast:
4	chr5:117089885..117092759-chr5:117093000..117095939,2	MCF-7	breast:
5	chr5:117050991..117053069-chr5:117068100..117070459,2	MCF-7	breast:
6	chr5:117080321..117081196-chr8:117848296..117848880,2	MCF-7	breast:
7	chr5:117077570..117079876-chr5:117081896..117084183,2	MCF-7	breast:
8	chr5:117112749..117115394-chr5:117119190..117122198,3	K562	blood:
9	chr5:117077570..117079876-chr5:117081896..117084183,2	MCF-7	breast:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-DTWD2-12	chr5:117114521-117115227	NONHSAT103390
2	lnc-DMXL1-4	chr5:117066056-117066103	NR_104997
3	lnc-DTWD2-13	chr5:117057573-117057792	NONHSAT103389
4	lnc-DTWD2-13	chr5:117054935-117055640	NONHSAT103389

No data

Variant related genes	Relation type
RPL7L1P4	TF binding region
ENSG00000251477	TF binding region
RPL7L1P4	CpG island
ENSG00000251477	CpG island
ENSG00000249582	chromatin interactions

Extended variants
information (count: 1527 )
Associated
traits (count: 73 )

Variant overlapped rSNPs/rCNVs (count:1527 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs377463163	chr5:117054938-117054939	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
2	rs572312627	chr5:117054982-117054983	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
3	rs547311749	chr5:117054985-117054986	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
4	rs80182302	chr5:117054986-117054987	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
5	rs17142939	chr5:117055037-117055038	Inactive region	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs181727019	chr5:117055041-117055042	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
7	rs186289535	chr5:117055042-117055043	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
8	rs189945738	chr5:117055110-117055111	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
9	rs1358226	chr5:117055145-117055146	Inactive region	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs546133938	chr5:117055182-117055183	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
11	rs531042906	chr5:117055192-117055193	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
12	rs368675304	chr5:117055218-117055219	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
13	rs180753660	chr5:117055219-117055220	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
14	rs569632580	chr5:117055223-117055224	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
15	rs562110389	chr5:117055230-117055231	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
16	rs531047800	chr5:117055263-117055264	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
17	rs536666305	chr5:117055264-117055265	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
18	rs551076451	chr5:117055323-117055324	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
19	rs113234958	chr5:117055359-117055360	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
20	rs147683826	chr5:117055364-117055365	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
21	rs539834826	chr5:117055419-117055420	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
22	rs546977013	chr5:117055428-117055429	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
23	rs186139561	chr5:117055431-117055432	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
24	rs79119598	chr5:117055439-117055440	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
25	rs113513408	chr5:117055482-117055483	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
26	rs190727875	chr5:117055525-117055526	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
27	rs148719030	chr5:117055557-117055558	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
28	rs368592231	chr5:117055604-117055605	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
29	rs536778196	chr5:117055615-117055616	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
30	rs183262809	chr5:117055636-117055637	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
31	rs545008366	chr5:117057575-117057576	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
32	rs564909079	chr5:117057646-117057647	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
33	rs376813371	chr5:117057658-117057659	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
34	rs577876793	chr5:117057663-117057664	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
35	rs540506145	chr5:117057685-117057686	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
36	rs184127124	chr5:117057708-117057709	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
37	rs529082689	chr5:117057710-117057711	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
38	rs549139881	chr5:117057722-117057723	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
39	rs562579472	chr5:117057750-117057751	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
40	rs147272712	chr5:117057753-117057754	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
41	rs188149446	chr5:117057755-117057756	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
42	rs139770388	chr5:117057762-117057763	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
43	rs116137276	chr5:117057782-117057783	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
44	rs548045306	chr5:117057785-117057786	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
45	rs562626926	chr5:117066085-117066086	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
46	rs185877618	chr5:117066103-117066104	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
47	rs548615562	chr5:117066225-117066226	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs568448343	chr5:117066229-117066230	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs115300885	chr5:117066258-117066259	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs182712326	chr5:117066262-117066263	Enhancers	n/a	n/a	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
Breast cancer	21509527	CNVD
Autism	22543975	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:64 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:117066200-117069200	Enhancers	Fetal Lung	lung
2	chr5:117066400-117068400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
3	chr5:117066600-117067400	Enhancers	Rectal Smooth Muscle	rectum
4	chr5:117067000-117067600	Enhancers	Fetal Stomach	stomach
5	chr5:117067000-117067800	Enhancers	Fetal Intestine Small	intestine
6	chr5:117067000-117068600	Enhancers	Colon Smooth Muscle	Colon
7	chr5:117067200-117068200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr5:117067400-117067800	Enhancers	Fetal Brain Male	brain
9	chr5:117067400-117068200	Enhancers	Stomach Smooth Muscle	stomach
10	chr5:117067400-117068400	Weak transcription	Rectal Smooth Muscle	rectum
11	chr5:117067800-117069200	Weak transcription	Fetal Intestine Small	intestine
12	chr5:117068000-117069400	Enhancers	Ovary	ovary
13	chr5:117068200-117068600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
14	chr5:117068600-117068800	Enhancers	Lung	lung
15	chr5:117068600-117068800	Enhancers	Rectal Smooth Muscle	rectum
16	chr5:117068600-117069000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
17	chr5:117069200-117069600	Enhancers	Fetal Intestine Small	intestine
18	chr5:117069200-117069600	Weak transcription	Fetal Lung	lung
19	chr5:117069600-117069800	Enhancers	Fetal Lung	lung
20	chr5:117069600-117070600	Weak transcription	Fetal Intestine Small	intestine
21	chr5:117069800-117071800	Weak transcription	Fetal Lung	lung
22	chr5:117070600-117070800	Enhancers	Fetal Intestine Large	intestine
23	chr5:117070800-117071000	Enhancers	Fetal Intestine Small	intestine
24	chr5:117071800-117072200	Enhancers	Fetal Lung	lung
25	chr5:117072200-117073800	Weak transcription	Fetal Lung	lung
26	chr5:117073800-117074000	Enhancers	Fetal Lung	lung
27	chr5:117074600-117075800	Enhancers	Brain Germinal Matrix	brain
28	chr5:117074800-117076000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
29	chr5:117075400-117076200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
30	chr5:117075600-117076000	Enhancers	Brain Substantia Nigra	brain
31	chr5:117077000-117078400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
32	chr5:117077400-117077600	Enhancers	Right Atrium	heart
33	chr5:117077600-117078400	Enhancers	Ovary	ovary
34	chr5:117078200-117078400	Enhancers	Right Atrium	heart
35	chr5:117083800-117085200	Enhancers	HUES64 Cell Line	embryonic stem cell
36	chr5:117083800-117085600	Enhancers	ES-I3 Cell Line	embryonic stem cell
37	chr5:117084000-117084400	Enhancers	HUES6 Cell Line	embryonic stem cell
38	chr5:117084000-117085000	Enhancers	HUES48 Cell Line	embryonic stem cell
39	chr5:117084000-117085200	Enhancers	iPS-18 Cell Line	embryonic stem cell
40	chr5:117084400-117084800	Active TSS	HUES6 Cell Line	embryonic stem cell
41	chr5:117084400-117085200	Enhancers	iPS-15b Cell Line	embryonic stem cell
42	chr5:117084800-117085000	Enhancers	HUES6 Cell Line	embryonic stem cell
43	chr5:117095000-117095600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
44	chr5:117095000-117099000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
45	chr5:117095600-117095800	Enhancers	Small Intestine	intestine
46	chr5:117095600-117096200	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
47	chr5:117095600-117098800	Enhancers	Primary hematopoietic stem cells short term culture	blood
48	chr5:117096200-117098800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
49	chr5:117097000-117097600	Enhancers	Primary monocytes fromperipheralblood	blood
50	chr5:117097600-117097800	Enhancers	Brain Hippocampus Middle	brain

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links