Variant report

Variant	rs7147450
Chromosome Location	chr14:105488819-105488820
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:20)
CpG islands
(count:0)
Chromatin interactive
region (count:16)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:20 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	FOSL2	chr14:105488513-105489004	A549	lung:	n/a	n/a
2	POLR2A	chr14:105485371-105492836	U87	brain:	n/a	n/a
3	POLR2A	chr14:105487046-105490796	U87	brain:	n/a	n/a
4	STAT3	chr14:105487978-105488909	MCF10A-Er-Src	breast:	n/a	chr14:105488214-105488225
5	POLR2A	chr14:105486906-105489115	HepG2	liver:	n/a	n/a
6	POLR2A	chr14:105487058-105490796	U87	brain:	n/a	n/a
7	MYC	chr14:105486499-105489196	A549	lung:	n/a	chr14:105487772-105487781 chr14:105487761-105487777 chr14:105488011-105488018 chr14:105487769-105487779 chr14:105488235-105488244 chr14:105487768-105487777 chr14:105487029-105487038 chr14:105488007-105488020
8	RCOR1	chr14:105488729-105488860	K562	blood:	n/a	n/a
9	CTCF	chr14:105488792-105488861	LNCaP	prostate:	n/a	n/a
10	POLR2A	chr14:105486986-105488995	MCF10A-Er-Src	breast:	n/a	n/a
11	MXI1	chr14:105485485-105488889	IMR90	lung:	n/a	chr14:105487771-105487780 chr14:105487769-105487778
12	POLR2A	chr14:105487045-105489018	PANC-1	pancreas:	n/a	n/a
13	POLR2A	chr14:105487668-105488960	GM12878	blood:	n/a	n/a
14	POLR2A	chr14:105486315-105488995	SK-N-MC	brain:	n/a	n/a
15	FOS	chr14:105488696-105488933	MCF10A-Er-Src	breast:	n/a	n/a
16	POLR2A	chr14:105487680-105488830	GM12892	blood:	n/a	n/a
17	FOS	chr14:105488727-105488978	MCF10A-Er-Src	breast:	n/a	n/a
18	JUND	chr14:105488646-105488918	K562	blood:	n/a	n/a
19	POLR2A	chr14:105487644-105492830	U87	brain:	n/a	n/a
20	POLR2A	chr14:105487632-105489041	GM12892	blood:	n/a	n/a

No data

(count:16 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr14:105448840..105458160-chr14:105477229..105492100,32	MCF-7	breast:
2	chr14:105486497..105489125-chr17:57923024..57925819,2	MCF-7	breast:
3	chr1:32478407..32481120-chr14:105486396..105489029,2	MCF-7	breast:
4	chr14:105487916..105489481-chr16:89626019..89628336,2	MCF-7	breast:
5	chr14:105486934..105489265-chr14:106372865..106374868,2	MCF-7	breast:
6	chr14:105440890..105445623-chr14:105485614..105489562,6	MCF-7	breast:
7	chr14:105487778..105490193-chr14:105767272..105770165,2	MCF-7	breast:
8	chr14:105487751..105489658-chr14:105685991..105688181,2	MCF-7	breast:
9	chr14:105346758..105349135-chr14:105488164..105490065,2	MCF-7	breast:
10	chr14:105452399..105454814-chr14:105486903..105489011,2	K562	blood:
11	chr14:105488320..105490306-chr14:105542807..105544380,2	MCF-7	breast:
12	chr14:105487558..105490083-chr14:105516106..105518275,3	MCF-7	breast:
13	chr14:105433937..105458439-chr14:105476653..105492775,70	MCF-7	breast:
14	chr14:105486944..105489300-chr14:105953502..105956286,2	MCF-7	breast:
15	chr14:105487927..105490765-chr17:57920099..57922115,2	MCF-7	breast:
16	chr14:105329781..105332832-chr14:105486734..105489071,3	MCF-7	breast:

No data

Variant related genes	Relation type
CDCA4	TF binding region
ENSG00000185347	Chromatin interaction
ENSG00000121774	Chromatin interaction
ENSG00000185024	Chromatin interaction
ENSG00000167526	Chromatin interaction
ENSG00000140104	Chromatin interaction
ENSG00000099814	Chromatin interaction
ENSG00000257341	Chromatin interaction
ENSG00000185567	Chromatin interaction
ENSG00000201524	Chromatin interaction
ENSG00000213145	Chromatin interaction
ENSG00000200084	Chromatin interaction
ENSG00000211925	Chromatin interaction

Extended variants
information (count: 64 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:41)

rs_ID	r²[population]
rs10131315	0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10137513	0.92[ASN][1000 genomes]
rs10138381	0.93[ASN][1000 genomes]
rs10150848	0.90[CHB][hapmap];0.98[CHD][hapmap];1.00[JPT][hapmap];0.92[ASN][1000 genomes]
rs10873553	0.94[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.84[AMR][1000 genomes];0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs11160829	0.94[CEU][hapmap];1.00[CHB][hapmap];0.94[GIH][hapmap];1.00[JPT][hapmap];0.94[MEX][hapmap];0.95[TSI][hapmap];0.89[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11160830	0.94[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.94[MEX][hapmap];1.00[TSI][hapmap];0.89[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11628851	0.88[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs11845745	0.86[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12896131	0.88[AMR][1000 genomes];0.94[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2241867	1.00[CHB][hapmap];0.90[JPT][hapmap];0.94[ASN][1000 genomes]
rs2247140	0.91[AMR][1000 genomes];0.94[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2582567	0.94[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.84[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2582568	0.89[AMR][1000 genomes];0.94[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2582569	0.89[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs3204172	0.94[CEU][hapmap];1.00[CHB][hapmap];0.98[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.94[MEX][hapmap];0.95[TSI][hapmap];0.89[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3204173	0.94[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.94[MEX][hapmap];1.00[TSI][hapmap];0.89[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3923887	0.89[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4073652	0.94[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.91[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4075086	0.89[AMR][1000 genomes];0.96[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4077684	0.81[AMR][1000 genomes];0.80[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs4267250	0.94[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4309336	0.94[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.89[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4344668	0.89[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4354858	0.88[AMR][1000 genomes];0.94[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4429223	0.94[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6420941	1.00[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.89[AMR][1000 genomes];0.94[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6576065	0.86[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs6576066	0.86[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs6576068	0.89[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7141972	0.93[AMR][1000 genomes];0.96[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7150384	0.95[AFR][1000 genomes];0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7155932	0.92[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7157046	0.88[AMR][1000 genomes];0.91[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs8010080	0.94[AMR][1000 genomes];0.96[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs8011377	0.94[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.89[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs8016434	0.82[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs8017794	0.89[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs8022294	0.94[CEU][hapmap];1.00[CHB][hapmap];0.98[CHD][hapmap];0.92[GIH][hapmap];1.00[JPT][hapmap];0.86[LWK][hapmap];0.94[MEX][hapmap];1.00[TSI][hapmap];0.90[AMR][1000 genomes];0.97[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs894039	0.94[CEU][hapmap];1.00[CHB][hapmap];0.93[CHD][hapmap];0.92[GIH][hapmap];1.00[JPT][hapmap];0.94[MEX][hapmap];1.00[TSI][hapmap];0.89[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs9652406	0.83[AMR][1000 genomes];0.88[EUR][1000 genomes];0.92[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:23 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv1828345	chr14:105100787-105803170	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	165 gene(s)	inside rSNPs	diseases
2	nsv542225	chr14:105133688-105803170	Enhancers Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Weak transcription Active TSS Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	165 gene(s)	inside rSNPs	diseases
3	nsv542227	chr14:105157572-105803170	Enhancers Flanking Active TSS Genic enhancers Weak transcription Active TSS Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	147 gene(s)	inside rSNPs	diseases
4	nsv917106	chr14:105339195-105803170	Enhancers Flanking Active TSS Weak transcription Active TSS Bivalent Enhancer Bivalent/Poised TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	94 gene(s)	inside rSNPs	diseases
5	nsv902419	chr14:105381763-105494262	Bivalent Enhancer Weak transcription Flanking Active TSS Active TSS Strong transcription Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	59 gene(s)	inside rSNPs	diseases
6	nsv456457	chr14:105404384-105555396	Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Strong transcription Weak transcription Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	63 gene(s)	inside rSNPs	diseases
7	nsv566141	chr14:105404384-105555396	Weak transcription Flanking Bivalent TSS/Enh Active TSS Enhancers Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	63 gene(s)	inside rSNPs	diseases
8	nsv902420	chr14:105410183-105494262	Enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	56 gene(s)	inside rSNPs	diseases
9	nsv902421	chr14:105410183-105574843	Weak transcription Enhancers Genic enhancers Active TSS Flanking Active TSS Strong transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	73 gene(s)	inside rSNPs	diseases
10	nsv902422	chr14:105420215-105803170	Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Active TSS Genic enhancers ZNF genes & repeats Strong transcription Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	88 gene(s)	inside rSNPs	diseases
11	nsv1052190	chr14:105423761-105722653	Weak transcription Enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	81 gene(s)	inside rSNPs	diseases
12	nsv902423	chr14:105430890-105803170	Enhancers Bivalent Enhancer Flanking Active TSS Weak transcription Strong transcription Genic enhancers Active TSS ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	88 gene(s)	inside rSNPs	diseases
13	nsv1042303	chr14:105435649-105633544	Bivalent Enhancer Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Weak transcription Active TSS ZNF genes & repeats Strong transcription Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	73 gene(s)	inside rSNPs	diseases
14	nsv456458	chr14:105435649-105690092	Flanking Active TSS Weak transcription Enhancers Bivalent Enhancer Strong transcription Active TSS Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	77 gene(s)	inside rSNPs	diseases
15	nsv566150	chr14:105435649-105690092	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Active TSS Genic enhancers Flanking Bivalent TSS/Enh Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	77 gene(s)	inside rSNPs	diseases
16	nsv902424	chr14:105436222-105803170	Genic enhancers Weak transcription Enhancers Bivalent Enhancer Strong transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	86 gene(s)	inside rSNPs	diseases
17	nsv566151	chr14:105459140-105555396	Flanking Active TSS Weak transcription Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Active TSS Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	43 gene(s)	inside rSNPs	diseases
18	nsv456459	chr14:105459140-105617891	Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers Active TSS Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	55 gene(s)	inside rSNPs	diseases
19	nsv566152	chr14:105459140-105617891	Weak transcription Bivalent Enhancer Genic enhancers Strong transcription Enhancers Active TSS ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	55 gene(s)	inside rSNPs	diseases
20	nsv902425	chr14:105463936-105690092	Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Weak transcription ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	60 gene(s)	inside rSNPs	diseases
21	nsv983941	chr14:105485574-105534240	Enhancers Active TSS Flanking Active TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	37 gene(s)	inside rSNPs	diseases
22	esv3437595	chr14:105486432-105489280	Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Weak transcription Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	32 gene(s)	inside rSNPs	diseases
23	esv3416622	chr14:105486557-105488955	Flanking Active TSS Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	32 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:78 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:105485800-105489000	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr14:105486000-105489000	Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr14:105486000-105489000	Active TSS	GM12878-XiMat	blood
4	chr14:105486200-105489000	Active TSS	HUES64 Cell Line	embryonic stem cell
5	chr14:105486800-105489200	Active TSS	A549	lung
6	chr14:105487800-105489000	Flanking Active TSS	Muscle Satellite Cultured Cells	--
7	chr14:105487800-105489000	Flanking Active TSS	Dnd41	blood
8	chr14:105487800-105489000	Flanking Active TSS	NH-A	brain
9	chr14:105488000-105489000	Flanking Active TSS	Primary T cells from cord blood	blood
10	chr14:105488000-105489200	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
11	chr14:105488200-105489000	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
12	chr14:105488200-105489000	Flanking Active TSS	Hela-S3	cervix
13	chr14:105488400-105489000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
14	chr14:105488400-105489000	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
15	chr14:105488400-105489000	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
16	chr14:105488400-105489000	Enhancers	Brain Angular Gyrus	brain
17	chr14:105488400-105489000	Enhancers	Fetal Heart	heart
18	chr14:105488400-105492000	Enhancers	Monocytes-CD14+_RO01746	blood
19	chr14:105488400-105494000	Enhancers	Primary monocytes fromperipheralblood	blood
20	chr14:105488400-105496600	Weak transcription	Esophagus	oesophagus
21	chr14:105488400-105497400	Weak transcription	Gastric	stomach
22	chr14:105488600-105489000	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
23	chr14:105488600-105489000	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
24	chr14:105488600-105489000	Enhancers	Primary T helper naive cells from peripheral blood	blood
25	chr14:105488600-105489000	Enhancers	Primary T helper cells PMA-I stimulated	--
26	chr14:105488600-105489000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
27	chr14:105488600-105489000	Enhancers	Adipose Nuclei	Adipose
28	chr14:105488600-105489000	Enhancers	Duodenum Smooth Muscle	Duodenum
29	chr14:105488600-105489000	Enhancers	Fetal Intestine Large	intestine
30	chr14:105488600-105489000	Enhancers	Fetal Intestine Small	intestine
31	chr14:105488600-105489000	Enhancers	Fetal Thymus	thymus
32	chr14:105488600-105489000	ZNF genes & repeats	HUVEC	blood vessel
33	chr14:105488600-105489600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
34	chr14:105488600-105490400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
35	chr14:105488600-105490800	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
36	chr14:105488600-105491200	Weak transcription	Left Ventricle	heart
37	chr14:105488600-105491800	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
38	chr14:105488600-105491800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
39	chr14:105488600-105492400	Enhancers	NHDF-Ad	bronchial
40	chr14:105488600-105499200	Weak transcription	Rectal Smooth Muscle	rectum
41	chr14:105488600-105499200	Weak transcription	Sigmoid Colon	Sigmoid Colon
42	chr14:105488800-105489000	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
43	chr14:105488800-105489000	Active TSS	iPS-20b Cell Line	embryonic stem cell
44	chr14:105488800-105489000	Enhancers	Breast Myoepithelial Primary Cells	Breast
45	chr14:105488800-105489000	Enhancers	Primary hematopoietic stem cells short term culture	blood
46	chr14:105488800-105489000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
47	chr14:105488800-105489000	Enhancers	Duodenum Mucosa	Duodenum
48	chr14:105488800-105489000	Enhancers	Fetal Lung	lung
49	chr14:105488800-105489000	Enhancers	HepG2	liver
50	chr14:105488800-105489200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin

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