Variant report

Variant	nsv459989
Chromosome Location	chr2:188308640-188318187
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	chr2:188317827-188318187	K562	blood:	n/a	n/a
2	ATF2	chr2:188312809-188313314	H1-hESC	embryonic stem cell:	n/a	n/a
3	BCLAF1	chr2:188312648-188313438	GM12878	blood:	n/a	n/a
4	BCLAF1	chr2:188312732-188313340	GM12878	blood:	n/a	n/a
5	BHLHE40	chr2:188312812-188313323	GM12878	blood:	n/a	n/a
6	BRCA1	chr2:188313072-188313272	GM12878	blood:	n/a	n/a
7	CBX3	chr2:188312772-188313268	K562	blood:	n/a	n/a
8	CBX3	chr2:188312808-188313187	HCT-116	colon:	n/a	n/a
9	CBX3	chr2:188312818-188313395	HCT-116	colon:	n/a	n/a
10	CEBPB	chr2:188312869-188313236	IMR90	lung:	n/a	n/a
11	CEBPB	chr2:188314794-188314995	K562	blood:	n/a	chr2:188314843-188314854
12	CEBPB	chr2:188312799-188313229	ECC-1	luminal epithelium:	n/a	n/a
13	CEBPB	chr2:188314779-188314995	IMR90	lung:	n/a	chr2:188314843-188314854
14	CEBPB	chr2:188312883-188313212	K562	blood:	n/a	n/a
15	CEBPB	chr2:188312878-188313270	H1-hESC	embryonic stem cell:	n/a	n/a
16	CEBPB	chr2:188312895-188313248	Hela-S3	cervix:	n/a	n/a
17	CEBPB	chr2:188314715-188314989	A549	lung:	n/a	chr2:188314843-188314854 chr2:188314745-188314757
18	CEBPB	chr2:188312961-188313147	K562	blood:	n/a	n/a
19	CEBPB	chr2:188314800-188314996	HepG2	liver:	n/a	chr2:188314843-188314854
20	CEBPB	chr2:188312955-188313166	MCF-7	breast:	n/a	n/a
21	CEBPB	chr2:188312901-188313183	HepG2	liver:	n/a	n/a
22	CEBPB	chr2:188312856-188313215	K562	blood:	n/a	n/a
23	CHD1	chr2:188312848-188313460	GM12878	blood:	n/a	n/a
24	CHD2	chr2:188312761-188313306	GM12878	blood:	n/a	n/a
25	CREB1	chr2:188312779-188313289	H1-hESC	embryonic stem cell:	n/a	n/a
26	CREB1	chr2:188312758-188313327	GM12878	blood:	n/a	n/a
27	CREB1	chr2:188312721-188313388	GM12878	blood:	n/a	n/a
28	CTCF	chr2:188317860-188318109	HUVEC	blood vessel:	n/a	chr2:188317981-188317999 chr2:188317976-188317997 chr2:188317982-188317998 chr2:188317986-188317994
29	CTCF	chr2:188317847-188318142	K562	blood:	n/a	chr2:188317981-188317999 chr2:188317976-188317997 chr2:188317982-188317998 chr2:188317986-188317994
30	CTCF	chr2:188312880-188313030	HCPEpiC	choroid plexus:	n/a	n/a
31	CTCF	chr2:188317920-188318070	SAEC	small airway:	n/a	chr2:188317981-188317999 chr2:188317976-188317997 chr2:188317982-188317998 chr2:188317986-188317994
32	CTCF	chr2:188317900-188318050	GM12867	blood:	n/a	chr2:188317981-188317999 chr2:188317976-188317997 chr2:188317982-188317998 chr2:188317986-188317994
33	CTCF	chr2:188317779-188318198	MCF-7	breast:	n/a	chr2:188317981-188317999 chr2:188317976-188317997 chr2:188317982-188317998 chr2:188317986-188317994
34	CTCF	chr2:188312891-188313096	GM12878	blood:	n/a	n/a
35	CTCF	chr2:188317900-188318050	HVMF	connective:	n/a	chr2:188317981-188317999 chr2:188317976-188317997 chr2:188317982-188317998 chr2:188317986-188317994
36	CTCF	chr2:188318160-188318310	HPF	lung:	n/a	n/a
37	CTCF	chr2:188312840-188312990	HPF	lung:	n/a	n/a
38	CTCF	chr2:188312980-188313130	AoAF	blood vessel:	n/a	n/a
39	CTCF	chr2:188313000-188313150	AG10803	skin:	n/a	n/a
40	CTCF	chr2:188313040-188313190	HRE	kidney:	n/a	n/a
41	CTCF	chr2:188317820-188317970	RPTEC	kidney:	n/a	n/a
42	CTCF	chr2:188313060-188313210	NHEK	skin:	n/a	n/a
43	CTCF	chr2:188317900-188318050	HMF	breast:	n/a	chr2:188317981-188317999 chr2:188317976-188317997 chr2:188317982-188317998 chr2:188317986-188317994
44	CTCF	chr2:188317920-188318070	HRE	kidney:	n/a	chr2:188317981-188317999 chr2:188317976-188317997 chr2:188317982-188317998 chr2:188317986-188317994
45	CTCF	chr2:188317789-188318139	HepG2	liver:	n/a	chr2:188317981-188317999 chr2:188317976-188317997 chr2:188317982-188317998 chr2:188317986-188317994
46	CTCF	chr2:188317920-188318060	LNCaP	prostate:	n/a	chr2:188317981-188317999 chr2:188317976-188317997 chr2:188317982-188317998 chr2:188317986-188317994
47	CTCF	chr2:188313000-188313150	HEK293	kidney:	n/a	n/a
48	CTCF	chr2:188312940-188313090	WERI-Rb-1	eye:	n/a	n/a
49	CTCF	chr2:188312771-188313251	GM12878	blood:	n/a	n/a
50	CTCF	chr2:188312943-188312991	GM13976	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:188312833-188312883	AG10803	skin:	n/a
2	chr2:188312833-188312883	HUVEC	blood vessel:	n/a
3	chr2:188312833-188312883	HCM	heart:	n/a
4	chr2:188312833-188312883	HEEpiC	esophagus:	n/a
5	chr2:188312833-188312883	HCPEpiC	choroid plexus:	n/a
6	chr2:188312833-188312883	U87	brain:	n/a
7	chr2:188312833-188312883	MCF10A-Er-Src	breast:	n/a
8	chr2:188312833-188312883	HCT-116	colon:	n/a
9	chr2:188312833-188312883	IMR90	lung:	fetal
10	chr2:188312833-188312883	SK-N-SH	brain:	n/a
11	chr2:188312833-188312883	NHBE	bronchial:	n/a
12	chr2:188312833-188312883	BE2_C	brain:	n/a
13	chr2:188312833-188312883	Hela-S3	cervix:	n/a
14	chr2:188312833-188312883	HMEC	breast:	n/a
15	chr2:188312833-188312883	NB4	blood:	n/a
16	chr2:188312833-188312883	HEK293	kidney:	embryo
17	chr2:188312833-188312883	SK-N-MC	brain:	n/a
18	chr2:188312833-188312883	NT2-D1	testis:	n/a
19	chr2:188312833-188312883	T-47D	breast:	n/a
20	chr2:188312833-188312883	GM19239	blood:	n/a
21	chr2:188312833-188312883	HPAEpiC	pulmonary alveolar:	n/a
22	chr2:188312833-188312883	K562	blood:	n/a
23	chr2:188312833-188312883	AG04449	skin:	fetal
24	chr2:188312833-188312883	HNPCEpiC	eye:	n/a
25	chr2:188312833-188312883	ECC-1	luminal epithelium:	n/a
26	chr2:188312833-188312883	Caco-2	colon:	n/a
27	chr2:188312833-188312883	LNCaP	prostate:	n/a
28	chr2:188312833-188312883	AG09319	gingival:	n/a
29	chr2:188312833-188312883	SAEC	small airway:	n/a
30	chr2:188312833-188312883	GM12891	blood:	n/a
31	chr2:188312833-188312883	PANC-1	pancreas:	n/a
32	chr2:188312833-188312883	AG04450	lung:	fetal
33	chr2:188312833-188312883	BJ	skin:	n/a
34	chr2:188312833-188312883	HCF	heart:	n/a
35	chr2:188312833-188312883	SKMC	muscle:	n/a
36	chr2:188312833-188312883	HAEpiC	amniotic membrane:	n/a
37	chr2:188312833-188312883	HRPEpiC	eye:	n/a
38	chr2:188312833-188312883	GM06990	blood:	n/a
39	chr2:188312833-188312883	HL-60	blood:	n/a
40	chr2:188312833-188312883	RPTEC	kidney:	n/a
41	chr2:188312833-188312883	MCF-7	breast:	n/a
42	chr2:188312833-188312883	CMK	blood:	n/a
43	chr2:188312833-188312883	HepG2	liver:	n/a
44	chr2:188312833-188312883	HRE	kidney:	n/a
45	chr2:188312833-188312883	SK-N-SH_RA	brain:	n/a
46	chr2:188312833-188312883	NHDF-neo	bronchial:	n/a
47	chr2:188312833-188312883	A549	lung:	n/a
48	chr2:188312833-188312883	GM12892	blood:	n/a
49	chr2:188312833-188312883	NH-A	brain:	n/a
50	chr2:188312833-188312883	Jurkat	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr2:188316887..188320656-chr2:188322905..188325832,3	K562	blood:
2	chr2:188307594..188309818-chr2:188311954..188314639,2	K562	blood:
3	chr2:187727496..187728175-chr2:188317935..188318450,2	K562	blood:
4	chr2:188313751..188315339-chr2:188318942..188321717,2	K562	blood:
5	chr2:188163616..188164504-chr2:188317553..188318396,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TFPI-1	chr2:188312766-188312873	NONHSAT076019
2	lnc-TFPI-1	chr2:188312766-188312979	NONHSAT076015
3	lnc-TFPI-1	chr2:188312766-188312979	NONHSAT076017
4	lnc-TFPI-1	chr2:188312766-188312980	NONHSAT076016

Variant related genes	Relation type
CALCRL	TF binding region
CALCRL	CpG island
ENSG00000064989	chromatin interactions

Extended variants
information (count: 278 )
Associated
traits (count: 50 )

Variant overlapped rSNPs/rCNVs (count:278 , 50 per page) page: 1 2 3 4 5 6

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs3771063	chr2:188308640-188308641	Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs193261028	chr2:188308642-188308643	Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs185043287	chr2:188308715-188308716	Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs111678343	chr2:188308726-188308727	Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs7595610	chr2:188308741-188308742	Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs114829206	chr2:188308751-188308752	Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs557027136	chr2:188308780-188308781	Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs569975062	chr2:188308797-188308798	Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs537305301	chr2:188308826-188308827	Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs41393945	chr2:188308853-188308854	Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs577136805	chr2:188308882-188308883	Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs141124130	chr2:188308941-188308942	Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs553081747	chr2:188309015-188309016	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs574404843	chr2:188309067-188309068	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs541821159	chr2:188309068-188309069	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs114260125	chr2:188309154-188309155	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs531132343	chr2:188309171-188309172	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs546116890	chr2:188309202-188309203	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs189031754	chr2:188309228-188309229	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs528702887	chr2:188309254-188309255	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs181638617	chr2:188309255-188309256	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs568543438	chr2:188309373-188309374	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs375934801	chr2:188309407-188309408	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs550966556	chr2:188309409-188309410	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs185419264	chr2:188309431-188309432	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs188707488	chr2:188309472-188309473	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs180846698	chr2:188309514-188309515	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs558922772	chr2:188309545-188309546	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs534140919	chr2:188309571-188309572	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs558589289	chr2:188309675-188309676	Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs116429980	chr2:188309709-188309710	Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs186100907	chr2:188309730-188309731	Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs537872968	chr2:188309746-188309747	Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs115814384	chr2:188309750-188309751	Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs574493668	chr2:188309799-188309800	Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs541532385	chr2:188309808-188309809	Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs1912850	chr2:188309875-188309876	Weak transcription Flanking Active TSS Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs191827329	chr2:188309877-188309878	Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs370803241	chr2:188309913-188309914	Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs564487131	chr2:188309947-188309948	Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs573410269	chr2:188309979-188309980	Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs184124921	chr2:188310094-188310095	Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs1912849	chr2:188310118-188310119	Weak transcription Active TSS Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs35805822	chr2:188310189-188310190	Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs145073552	chr2:188310200-188310201	Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs551119775	chr2:188310219-188310220	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs541950471	chr2:188310255-188310256	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs1912848	chr2:188310305-188310306	Weak transcription Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
49	rs373384407	chr2:188310357-188310358	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs551755170	chr2:188310493-188310494	Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:50)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	21979893	CNVD
Ependymoma	16718352	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Melanoma	18172304	CNVD
Cancer	16751803	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Testicular germ cell tumor	18059402	CNVD
Breast cancer	16272173	CNVD
Ewing''s sarcoma	17952124	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Autism	16446308	CNVD
Autism	19401682	CNVD
Colorectal cancer	16272173	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Lung cancer	18438408	CNVD
Glioblastoma	21080181	CNVD
Prostate cancer	18632612	CNVD
Acute myeloid leukemia	20729466	CNVD
small cell lung cancer	20016488	CNVD
Facial dysmorphism	20548289	CNVD
Mental retardation	20548289	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Breast cancer	21364760	CNVD
Myelofibrosis	22110671	CNVD
Hirschsprung''s Disease	21712996	CNVD
Cancer	21183584	CNVD
Sudden cardiac death	19188705	CNVD
Autism	19329560	CNVD
Urothelial carcinoma	21177765	CNVD
Intellectual disability	22102821	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Tetralogy of Fallot	22912587	CNVD

Chromatin state (count:235 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:188269600-188309800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
2	chr2:188295200-188309600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
3	chr2:188299200-188311800	Weak transcription	Left Ventricle	heart
4	chr2:188300200-188312200	Weak transcription	NHLF	lung
5	chr2:188302200-188309000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
6	chr2:188303800-188310800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr2:188304000-188308800	Weak transcription	Adipose Nuclei	Adipose
8	chr2:188304200-188311200	Weak transcription	Ovary	ovary
9	chr2:188305800-188310800	Weak transcription	Fetal Kidney	kidney
10	chr2:188306600-188309600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
11	chr2:188307800-188310800	Weak transcription	Right Atrium	heart
12	chr2:188307800-188313200	Active TSS	Pancreatic Islets	Pancreatic Islet
13	chr2:188308400-188309000	Enhancers	Primary hematopoietic stem cells	blood
14	chr2:188308600-188309000	Transcr. at gene 5' and 3'	HUVEC	blood vessel
15	chr2:188308600-188313000	Active TSS	Fetal Muscle Leg	muscle
16	chr2:188308800-188309600	Enhancers	Adipose Nuclei	Adipose
17	chr2:188309000-188309400	Weak transcription	Primary hematopoietic stem cells	blood
18	chr2:188309000-188309400	Flanking Active TSS	HUVEC	blood vessel
19	chr2:188309000-188309600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
20	chr2:188309000-188310800	Weak transcription	Monocytes-CD14+_RO01746	blood
21	chr2:188309400-188309600	Enhancers	Primary hematopoietic stem cells	blood
22	chr2:188309400-188313000	Active TSS	HUVEC	blood vessel
23	chr2:188309600-188309800	Active TSS	Adipose Nuclei	Adipose
24	chr2:188309600-188310000	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
25	chr2:188309600-188310000	Flanking Active TSS	Primary hematopoietic stem cells	blood
26	chr2:188309600-188310000	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
27	chr2:188309600-188310000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
28	chr2:188309800-188310000	Flanking Active TSS	Adipose Nuclei	Adipose
29	chr2:188309800-188310200	Active TSS	Duodenum Smooth Muscle	Duodenum
30	chr2:188309800-188312800	Active TSS	Primary hematopoietic stem cells short term culture	blood
31	chr2:188310000-188310200	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
32	chr2:188310000-188310400	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
33	chr2:188310000-188310800	Active TSS	Primary hematopoietic stem cells	blood
34	chr2:188310000-188310800	Active TSS	Adipose Nuclei	Adipose
35	chr2:188310000-188311600	Weak transcription	Brain Inferior Temporal Lobe	brain
36	chr2:188310000-188313000	Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
37	chr2:188310200-188310400	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
38	chr2:188310200-188311000	Weak transcription	Duodenum Smooth Muscle	Duodenum
39	chr2:188310400-188310600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
40	chr2:188310400-188311200	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
41	chr2:188310400-188313200	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
42	chr2:188310600-188310800	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
43	chr2:188310800-188311000	Flanking Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
44	chr2:188310800-188311000	Flanking Active TSS	Primary hematopoietic stem cells	blood
45	chr2:188310800-188311000	Flanking Active TSS	Adipose Nuclei	Adipose
46	chr2:188310800-188311000	Enhancers	Monocytes-CD14+_RO01746	blood
47	chr2:188310800-188311600	Enhancers	Primary T cells from cord blood	blood
48	chr2:188310800-188312400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
49	chr2:188310800-188313000	Active TSS	Fetal Kidney	kidney
50	chr2:188310800-188313200	Active TSS	Brain Anterior Caudate	brain

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