Variant report

Variant	nsv882747
Chromosome Location	chr5:115566636-115662510
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:545)
CpG islands
(count:122)
Chromatin interactive
region (count:14)
LncRNA
region (count:10)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:545 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr5:115567073-115567351	HepG2	liver:	n/a	n/a
2	ATF1	chr5:115614176-115614178	K562	blood:	n/a	n/a
3	BACH1	chr5:115573174-115573254	H1-hESC	embryonic stem cell:	n/a	n/a
4	BATF	chr5:115609206-115609493	GM12878	blood:	n/a	chr5:115609356-115609366 chr5:115609352-115609362 chr5:115609355-115609366
5	BATF	chr5:115609200-115609492	GM12878	blood:	n/a	chr5:115609356-115609366 chr5:115609352-115609362 chr5:115609355-115609366
6	CBX3	chr5:115612653-115612965	K562	blood:	n/a	n/a
7	CBX3	chr5:115612735-115612979	K562	blood:	n/a	n/a
8	CBX3	chr5:115612612-115613059	HCT-116	colon:	n/a	n/a
9	CBX3	chr5:115644136-115644420	K562	blood:	n/a	n/a
10	CBX3	chr5:115644032-115644480	HCT-116	colon:	n/a	n/a
11	CBX3	chr5:115644114-115644421	K562	blood:	n/a	n/a
12	CEBPB	chr5:115612611-115612811	A549	lung:	n/a	n/a
13	CEBPB	chr5:115658782-115659034	HepG2	liver:	n/a	chr5:115658862-115658873
14	CEBPB	chr5:115608357-115608659	A549	lung:	n/a	chr5:115608483-115608494
15	CEBPB	chr5:115584119-115584488	MCF-7	breast:	n/a	chr5:115584298-115584309 chr5:115584300-115584311
16	CEBPB	chr5:115584226-115584373	HepG2	liver:	n/a	chr5:115584298-115584309 chr5:115584300-115584311
17	CEBPB	chr5:115608311-115608872	IMR90	lung:	n/a	chr5:115608483-115608494
18	CEBPB	chr5:115658862-115658938	A549	lung:	n/a	chr5:115658862-115658873
19	CEBPB	chr5:115601292-115601498	HepG2	liver:	n/a	n/a
20	CEBPB	chr5:115632480-115632726	HepG2	liver:	n/a	n/a
21	CEBPB	chr5:115635639-115636210	MCF-7	breast:	n/a	chr5:115635913-115635925
22	CEBPB	chr5:115608269-115608767	MCF-7	breast:	n/a	chr5:115608483-115608494
23	CEBPB	chr5:115615956-115616164	HepG2	liver:	n/a	n/a
24	CEBPB	chr5:115608381-115608622	HepG2	liver:	n/a	chr5:115608483-115608494
25	CEBPB	chr5:115608227-115608718	MCF-7	breast:	n/a	chr5:115608483-115608494
26	CEBPB	chr5:115584254-115584389	K562	blood:	n/a	chr5:115584298-115584309 chr5:115584300-115584311
27	CEBPB	chr5:115584135-115584482	HepG2	liver:	n/a	chr5:115584298-115584309 chr5:115584300-115584311
28	CHD2	chr5:115609186-115609453	GM12878	blood:	n/a	n/a
29	CHD2	chr5:115608466-115608624	GM12878	blood:	n/a	n/a
30	CTCF	chr5:115636920-115637070	GM12873	blood:	n/a	chr5:115637008-115637021 chr5:115637005-115637023 chr5:115637007-115637028
31	CTCF	chr5:115608340-115608490	AG09309	skin:	n/a	n/a
32	CTCF	chr5:115573740-115573890	NHLF	lung:	n/a	n/a
33	CTCF	chr5:115573720-115573870	BE2_C	brain:	n/a	n/a
34	CTCF	chr5:115573740-115573890	NHDF-neo	bronchial:	n/a	n/a
35	CTCF	chr5:115633280-115633430	HepG2	liver:	n/a	n/a
36	CTCF	chr5:115573700-115573850	HEK293	kidney:	n/a	n/a
37	CTCF	chr5:115625180-115625330	GM06990	blood:	n/a	n/a
38	CTCF	chr5:115608387-115608561	MCF-7	breast:	n/a	n/a
39	CTCF	chr5:115573740-115573890	HVMF	connective:	n/a	n/a
40	CTCF	chr5:115625120-115625270	MCF-7	breast:	n/a	chr5:115625169-115625182
41	CTCF	chr5:115625129-115625224	HUVEC	blood vessel:	n/a	chr5:115625169-115625182
42	CTCF	chr5:115641760-115641910	HCPEpiC	choroid plexus:	n/a	chr5:115641778-115641786
43	CTCF	chr5:115573751-115573867	HUVEC	blood vessel:	n/a	n/a
44	CTCF	chr5:115625120-115625270	HCPEpiC	choroid plexus:	n/a	chr5:115625169-115625182
45	CTCF	chr5:115573660-115573810	NHEK	skin:	n/a	n/a
46	CTCF	chr5:115625100-115625250	GM12868	blood:	n/a	chr5:115625169-115625182
47	CTCF	chr5:115608320-115608470	HFF	foreskin:	n/a	n/a
48	CTCF	chr5:115633220-115633370	Caco-2	colon:	n/a	n/a
49	CTCF	chr5:115608409-115608558	Kidney_OC	kidney:	n/a	n/a
50	CTCF	chr5:115608380-115608530	HPAF	blood vessel:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:115639617-115639667	AG04449	skin:	fetal
2	chr5:115639617-115639667	NH-A	brain:	n/a
3	chr5:115599680-115599730	NHDF-neo	bronchial:	n/a
4	chr5:115599680-115599730	U87	brain:	n/a
5	chr5:115599680-115599730	BE2_C	brain:	n/a
6	chr5:115639617-115639667	HRE	kidney:	n/a
7	chr5:115639617-115639667	HIPEpiC	eye:	n/a
8	chr5:115599680-115599730	HepG2	liver:	n/a
9	chr5:115599680-115599730	HEK293	kidney:	embryo
10	chr5:115639617-115639667	HCF	heart:	n/a
11	chr5:115599680-115599730	HPAEpiC	pulmonary alveolar:	n/a
12	chr5:115639617-115639667	HMEC	breast:	n/a
13	chr5:115639617-115639667	GM06990	blood:	n/a
14	chr5:115639617-115639667	MCF10A-Er-Src	breast:	n/a
15	chr5:115639617-115639667	HEK293	kidney:	embryo
16	chr5:115639617-115639667	NB4	blood:	n/a
17	chr5:115599680-115599730	H1-hESC	embryonic stem cell:	embryo
18	chr5:115639617-115639667	HCPEpiC	choroid plexus:	n/a
19	chr5:115639617-115639667	SKMC	muscle:	n/a
20	chr5:115599680-115599730	GM12878	blood:	n/a
21	chr5:115599680-115599730	SK-N-SH	brain:	n/a
22	chr5:115639617-115639667	ProgFib	skin:	n/a
23	chr5:115599680-115599730	AG09309	skin:	n/a
24	chr5:115639617-115639667	HCM	heart:	n/a
25	chr5:115599680-115599730	GM06990	blood:	n/a
26	chr5:115599680-115599730	SAEC	small airway:	n/a
27	chr5:115639617-115639667	AG09319	gingival:	n/a
28	chr5:115599680-115599730	HCF	heart:	n/a
29	chr5:115639617-115639667	ECC-1	luminal epithelium:	n/a
30	chr5:115599680-115599730	GM19239	blood:	n/a
31	chr5:115599680-115599730	AoSMC	blood vessel:	n/a
32	chr5:115599680-115599730	PANC-1	pancreas:	n/a
33	chr5:115599680-115599730	ovcar-3	ovarian:	n/a
34	chr5:115639617-115639667	AG04450	lung:	fetal
35	chr5:115599680-115599730	T-47D	breast:	n/a
36	chr5:115639617-115639667	H1-hESC	embryonic stem cell:	embryo
37	chr5:115639617-115639667	RPTEC	kidney:	n/a
38	chr5:115639617-115639667	Hela-S3	cervix:	n/a
39	chr5:115599680-115599730	IMR90	lung:	fetal
40	chr5:115599680-115599730	HRE	kidney:	n/a
41	chr5:115599680-115599730	NHBE	bronchial:	n/a
42	chr5:115639617-115639667	AoSMC	blood vessel:	n/a
43	chr5:115639617-115639667	SAEC	small airway:	n/a
44	chr5:115639617-115639667	HAEpiC	amniotic membrane:	n/a
45	chr5:115599680-115599730	BJ	skin:	n/a
46	chr5:115599680-115599730	PrEC	prostate:	n/a
47	chr5:115599680-115599730	HNPCEpiC	eye:	n/a
48	chr5:115599680-115599730	AG09319	gingival:	n/a
49	chr5:115599680-115599730	AG04450	lung:	fetal
50	chr5:115639617-115639667	HRPEpiC	eye:	n/a

(count:14 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr5:115473058..115473763-chr5:115624723..115625238,2	MCF-7	breast:
2	chr5:115647669..115649812-chr5:115683571..115685304,2	K562	blood:
3	chr5:115573428..115574084-chr5:115607901..115608709,2	MCF-7	breast:
4	chr5:115632385..115634405-chr5:115635053..115637473,2	K562	blood:
5	chr5:115607181..115609929-chr5:115613382..115615949,2	K562	blood:
6	chr5:115573428..115574084-chr5:115607901..115608709,2	MCF-7	breast:
7	chr5:115611187..115613784-chr5:115614610..115617269,2	MCF-7	breast:
8	chr5:115473639..115474170-chr5:115607611..115608509,2	MCF-7	breast:
9	chr5:115632385..115634405-chr5:115635053..115637473,2	K562	blood:
10	chr5:115611187..115613784-chr5:115614610..115617269,2	MCF-7	breast:
11	chr5:115607181..115609929-chr5:115613382..115615949,2	K562	blood:
12	chr5:115630950..115633524-chr5:115633964..115636710,2	MCF-7	breast:
13	chr5:115630950..115633524-chr5:115633964..115636710,2	MCF-7	breast:
14	chr20:47537809..47538621-chr5:115628215..115629028,2	MCF-7	breast:

(count:10 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-LVRN.1-4	chr5:115637354-115638100	NONHSAT103359
2	lnc-COMMD10-6	chr5:115661716-115661988	l_3000_chr5:115661715-115668338_thyroid
3	lnc-LVRN.1-4	chr5:115632111-115632653	NONHSAT103359
4	lnc-LVRN.1-4	chr5:115633944-115634089	NONHSAT103359
5	lnc-LVRN.1-4	chr5:115628154-115628257	NONHSAT103358
6	lnc-LVRN.1-4	chr5:115643332-115643482	NONHSAT103359
7	lnc-LVRN.1-4	chr5:115641553-115642622	NONHSAT103359
8	lnc-LVRN.1-4	chr5:115639227-115639380	NONHSAT103358
9	lnc-LVRN.1-4	chr5:115638966-115639380	NONHSAT103359
10	lnc-LVRN.1-4	chr5:115633944-115634089	NONHSAT103358

No data

Variant related genes	Relation type
COMMD10	TF binding region
ENSG00000250015	TF binding region
COMMD10	CpG island
ENSG00000250015	CpG island
ENSG00000124198	chromatin interactions

Extended variants
information (count: 4838 )
Associated
traits (count: 75 )

Variant overlapped rSNPs/rCNVs (count:4838 , 50 per page) page: 1 2 3 4 5 6 7 ... 97

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6594958	chr5:115566636-115566637	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs533784493	chr5:115566661-115566662	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs369734956	chr5:115566669-115566670	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs535705906	chr5:115566701-115566702	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs553760549	chr5:115566712-115566713	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs574032723	chr5:115566747-115566748	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs148835161	chr5:115566763-115566764	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs370368148	chr5:115566765-115566766	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs562737392	chr5:115566772-115566773	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs576134788	chr5:115566849-115566850	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs143601568	chr5:115566861-115566862	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs549318994	chr5:115566931-115566932	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs113340692	chr5:115566954-115566955	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs527741065	chr5:115566955-115566956	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs541032386	chr5:115566976-115566977	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs187624310	chr5:115566986-115566987	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs191900107	chr5:115566989-115566990	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs550817110	chr5:115567017-115567018	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs141793492	chr5:115567021-115567022	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs147184376	chr5:115567024-115567025	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs570256481	chr5:115567039-115567040	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs371635118	chr5:115567050-115567051	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs114439527	chr5:115567078-115567079	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs552703562	chr5:115567100-115567101	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs568145219	chr5:115567132-115567133	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs111251903	chr5:115567147-115567148	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs183050922	chr5:115567172-115567173	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs143902986	chr5:115567177-115567178	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs186767132	chr5:115567197-115567198	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs190294256	chr5:115567236-115567237	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs147281152	chr5:115567248-115567249	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs113646903	chr5:115567272-115567273	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs558285503	chr5:115567281-115567282	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs572251261	chr5:115567282-115567283	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs143396161	chr5:115567293-115567294	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs376958826	chr5:115567298-115567299	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs182563204	chr5:115567356-115567357	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs541116128	chr5:115567358-115567359	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs376600906	chr5:115567362-115567363	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs58404617	chr5:115567376-115567377	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs58889682	chr5:115567414-115567415	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs543770607	chr5:115567415-115567416	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs542087997	chr5:115567427-115567428	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs6872739	chr5:115567444-115567445	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
45	rs371062717	chr5:115567446-115567447	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs559535031	chr5:115567458-115567459	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs143364440	chr5:115567478-115567479	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs149783695	chr5:115567496-115567497	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs187554512	chr5:115567509-115567510	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs527417601	chr5:115567528-115567529	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:75)

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
Sezary syndrome	18413736	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
Schizophrenia	23813976	CNVD

Chromatin state (count:1293 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:115551800-115576400	Weak transcription	Primary T helper cells fromperipheralblood	blood
2	chr5:115557400-115580800	Weak transcription	Primary T helper cells PMA-I stimulated	--
3	chr5:115557400-115583200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
4	chr5:115559200-115578400	Weak transcription	Fetal Lung	lung
5	chr5:115560400-115570400	Weak transcription	Primary B cells from peripheral blood	blood
6	chr5:115560400-115572600	Weak transcription	Fetal Intestine Small	intestine
7	chr5:115560400-115581000	Weak transcription	Primary T cells from cord blood	blood
8	chr5:115560400-115610600	Weak transcription	Left Ventricle	heart
9	chr5:115560600-115567600	Weak transcription	Primary hematopoietic stem cells	blood
10	chr5:115561400-115569400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
11	chr5:115561400-115580000	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
12	chr5:115561800-115586400	Weak transcription	Monocytes-CD14+_RO01746	blood
13	chr5:115562400-115572000	Weak transcription	Primary monocytes fromperipheralblood	blood
14	chr5:115562400-115589000	Weak transcription	Ovary	ovary
15	chr5:115563400-115571000	Weak transcription	Primary B cells from cord blood	blood
16	chr5:115565200-115569200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
17	chr5:115565600-115567000	Enhancers	Fetal Heart	heart
18	chr5:115566600-115567400	Enhancers	HepG2	liver
19	chr5:115568400-115578800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
20	chr5:115569200-115569400	Enhancers	Fetal Heart	heart
21	chr5:115569200-115569800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
22	chr5:115569400-115569600	Enhancers	Fetal Kidney	kidney
23	chr5:115569400-115569800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
24	chr5:115569600-115577600	Weak transcription	Fetal Kidney	kidney
25	chr5:115569800-115582200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
26	chr5:115571000-115573000	Strong transcription	Primary B cells from cord blood	blood
27	chr5:115571400-115572000	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
28	chr5:115572000-115580400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
29	chr5:115573000-115578800	Weak transcription	Primary B cells from cord blood	blood
30	chr5:115573400-115575000	Enhancers	Colon Smooth Muscle	Colon
31	chr5:115574000-115580000	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
32	chr5:115575000-115578200	Weak transcription	Colon Smooth Muscle	Colon
33	chr5:115576200-115576400	Enhancers	Adipose Nuclei	Adipose
34	chr5:115576200-115576600	Enhancers	HUVEC	blood vessel
35	chr5:115577600-115579600	Enhancers	Fetal Kidney	kidney
36	chr5:115577800-115578800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
37	chr5:115578000-115578800	Enhancers	Adipose Nuclei	Adipose
38	chr5:115578200-115578600	Enhancers	Liver	Liver
39	chr5:115578200-115578800	Enhancers	Colon Smooth Muscle	Colon
40	chr5:115578200-115579000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
41	chr5:115578400-115578600	Enhancers	Fetal Lung	lung
42	chr5:115578800-115579000	Enhancers	Primary T helper naive cells from peripheral blood	blood
43	chr5:115578800-115579600	Strong transcription	Primary B cells from cord blood	blood
44	chr5:115578800-115586000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
45	chr5:115579600-115581800	Weak transcription	Fetal Intestine Large	intestine
46	chr5:115579600-115610600	Weak transcription	Primary B cells from cord blood	blood
47	chr5:115580400-115580800	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
48	chr5:115581000-115581200	Strong transcription	Primary T cells from cord blood	blood
49	chr5:115581200-115581400	ZNF genes & repeats	Primary T cells from cord blood	blood
50	chr5:115581400-115591600	Weak transcription	Primary T cells from cord blood	blood

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