Variant report

Variant	rs1881998
Chromosome Location	chr3:121614175-121614176
allele	C/T
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	CEBPB	chr3:121614037-121614251	IMR90	lung:	n/a	chr3:121614186-121614199 chr3:121614188-121614199 chr3:121614186-121614199 chr3:121614188-121614199 chr3:121614186-121614199 chr3:121614186-121614197
2	MYC	chr3:121614054-121614188	NB4	blood:	n/a	n/a
3	RAD21	chr3:121614064-121614210	HepG2	liver:	n/a	n/a
4	CEBPB	chr3:121614004-121614413	MCF-7	breast:	n/a	chr3:121614186-121614199 chr3:121614188-121614199 chr3:121614186-121614199 chr3:121614188-121614199 chr3:121614186-121614199 chr3:121614186-121614197
5	CEBPD	chr3:121614021-121614275	HepG2	liver:	n/a	chr3:121614187-121614198
6	STAT3	chr3:121614130-121614250	MCF10A-Er-Src	breast:	n/a	n/a
7	FOS	chr3:121614044-121614281	MCF10A-Er-Src	breast:	n/a	n/a
8	E2F4	chr3:121614106-121614178	MCF10A-Er-Src	breast:	n/a	n/a
9	CEBPB	chr3:121613996-121614436	ECC-1	luminal epithelium:	n/a	chr3:121614186-121614199 chr3:121614188-121614199 chr3:121614186-121614199 chr3:121614188-121614199 chr3:121614186-121614199 chr3:121614186-121614197
10	STAT3	chr3:121613935-121614214	MCF10A-Er-Src	breast:	n/a	n/a
11	CEBPB	chr3:121613988-121614305	MCF-7	breast:	n/a	chr3:121614186-121614199 chr3:121614188-121614199 chr3:121614186-121614199 chr3:121614188-121614199 chr3:121614186-121614199 chr3:121614186-121614197
12	MYC	chr3:121613854-121614232	H1-hESC	embryonic stem cell:	n/a	n/a
13	CEBPB	chr3:121613986-121614254	HepG2	liver:	n/a	chr3:121614186-121614199 chr3:121614188-121614199 chr3:121614186-121614199 chr3:121614188-121614199 chr3:121614186-121614199 chr3:121614186-121614197
14	CEBPB	chr3:121614027-121614314	K562	blood:	n/a	chr3:121614186-121614199 chr3:121614188-121614199 chr3:121614186-121614199 chr3:121614188-121614199 chr3:121614186-121614199 chr3:121614186-121614197
15	CEBPB	chr3:121613983-121614358	HepG2	liver:	n/a	chr3:121614186-121614199 chr3:121614188-121614199 chr3:121614186-121614199 chr3:121614188-121614199 chr3:121614186-121614199 chr3:121614186-121614197
16	CEBPB	chr3:121613996-121614364	H1-hESC	embryonic stem cell:	n/a	chr3:121614186-121614199 chr3:121614188-121614199 chr3:121614186-121614199 chr3:121614188-121614199 chr3:121614186-121614199 chr3:121614186-121614197
17	CEBPB	chr3:121614021-121614340	ECC-1	luminal epithelium:	n/a	chr3:121614186-121614199 chr3:121614188-121614199 chr3:121614186-121614199 chr3:121614188-121614199 chr3:121614186-121614199 chr3:121614186-121614197
18	FOS	chr3:121614022-121614333	MCF10A-Er-Src	breast:	n/a	n/a
19	CEBPB	chr3:121614085-121614249	HepG2	liver:	n/a	chr3:121614186-121614199 chr3:121614188-121614199 chr3:121614186-121614199 chr3:121614188-121614199 chr3:121614186-121614199 chr3:121614186-121614197
20	CTCF	chr3:121614154-121614179	LNCaP	prostate:	n/a	n/a
21	CTCF	chr3:121614100-121614250	HMEC	breast:	n/a	n/a
22	FOS	chr3:121614022-121614284	MCF10A-Er-Src	breast:	n/a	n/a
23	FOS	chr3:121614023-121614331	MCF10A-Er-Src	breast:	n/a	n/a
24	CEBPB	chr3:121613998-121614338	HepG2	liver:	n/a	chr3:121614186-121614199 chr3:121614188-121614199 chr3:121614186-121614199 chr3:121614188-121614199 chr3:121614186-121614199 chr3:121614186-121614197
25	CEBPB	chr3:121614031-121614294	A549	lung:	n/a	chr3:121614186-121614199 chr3:121614188-121614199 chr3:121614186-121614199 chr3:121614188-121614199 chr3:121614186-121614199 chr3:121614186-121614197
26	CEBPB	chr3:121613989-121614353	Hela-S3	cervix:	n/a	chr3:121614186-121614199 chr3:121614188-121614199 chr3:121614186-121614199 chr3:121614188-121614199 chr3:121614186-121614199 chr3:121614186-121614197

Variant related genes	Relation type
SLC15A2	TF binding region

Extended variants
information (count: 86 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:78)

rs_ID	r²[population]
rs10470411	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10470412	0.91[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.86[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10511407	0.91[CEU][hapmap];1.00[CHD][hapmap];0.89[GIH][hapmap];0.82[JPT][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.97[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs10934561	0.91[CEU][hapmap];0.82[JPT][hapmap];0.84[EUR][1000 genomes]
rs11713268	0.93[AFR][1000 genomes];0.95[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11919421	0.91[CEU][hapmap];0.90[GIH][hapmap];0.86[TSI][hapmap]
rs12486309	0.90[EUR][1000 genomes]
rs12486310	0.92[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs12486456	0.91[CEU][hapmap];0.82[JPT][hapmap];0.80[EUR][1000 genomes]
rs12487516	0.86[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12488692	0.86[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12489142	0.86[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12489686	0.91[CEU][hapmap];0.88[CHD][hapmap];0.89[GIH][hapmap];0.82[JPT][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.81[EUR][1000 genomes]
rs12491109	0.91[CEU][hapmap];0.88[CHD][hapmap];0.89[GIH][hapmap];0.82[JPT][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.81[EUR][1000 genomes]
rs12492214	0.90[CEU][hapmap];0.82[JPT][hapmap];0.84[EUR][1000 genomes]
rs12492861	0.90[CEU][hapmap];1.00[CHB][hapmap]
rs12493270	0.90[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12629720	0.91[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.90[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12634458	0.90[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12636562	0.91[CEU][hapmap]
rs12695417	0.90[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13100245	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13321798	0.93[ASW][hapmap];0.91[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.92[TSI][hapmap];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1881997	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.95[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1920307	1.00[ASW][hapmap];0.91[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];0.93[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1920310	1.00[CHB][hapmap];0.89[GIH][hapmap]
rs2222826	0.84[EUR][1000 genomes]
rs2293613	1.00[CHB][hapmap];0.89[GIH][hapmap]
rs2689274	0.86[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2689278	0.91[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2689279	0.90[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2689280	0.91[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs2689286	0.86[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2700412	0.90[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2700413	0.91[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.86[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2700414	1.00[CHB][hapmap];1.00[JPT][hapmap];0.90[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2700419	0.86[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28844130	0.84[EUR][1000 genomes]
rs34241542	0.84[EUR][1000 genomes]
rs35354585	0.84[EUR][1000 genomes]
rs35692621	0.90[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35723704	0.90[AMR][1000 genomes];0.94[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs3805125	0.91[CEU][hapmap];0.88[CHD][hapmap];0.89[GIH][hapmap];0.82[JPT][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.87[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs3805129	0.81[CEU][hapmap];0.82[JPT][hapmap];0.87[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs3805132	0.86[AMR][1000 genomes];0.98[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs4048630	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs41271411	0.86[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4602434	1.00[CHB][hapmap];0.89[GIH][hapmap]
rs4603998	0.86[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4610269	0.91[CEU][hapmap];0.82[JPT][hapmap];0.86[AMR][1000 genomes];0.97[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs4676760	0.86[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4676761	0.91[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.86[AMR][1000 genomes];0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs4676762	0.95[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs57365001	0.90[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs57473053	0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs58485759	0.84[EUR][1000 genomes]
rs59064186	0.84[EUR][1000 genomes]
rs61567016	0.90[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6438681	0.91[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.90[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6798575	0.82[CEU][hapmap];0.90[GIH][hapmap];0.86[TSI][hapmap]
rs72959293	0.90[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72961314	0.90[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7619918	0.90[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7620562	0.82[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.90[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7625960	0.88[CEU][hapmap];1.00[JPT][hapmap];0.86[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7626052	0.91[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7627291	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7643293	0.91[CEU][hapmap]
rs7647585	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7650341	0.91[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.90[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9818733	0.86[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9831798	0.90[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9832735	0.90[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9834185	0.91[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.90[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9865926	0.90[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9869891	0.91[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.90[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9877671	0.86[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9882841	0.81[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv432480	chr3:121355723-121629928	Enhancers Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	39 gene(s)	inside rSNPs	diseases
2	nsv432482	chr3:121364236-121629634	Weak transcription ZNF genes & repeats Strong transcription Active TSS Genic enhancers Enhancers Transcr. at gene 5' and 3' Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	39 gene(s)	inside rSNPs	diseases
3	nsv432481	chr3:121364236-121637178	Weak transcription Strong transcription Genic enhancers Enhancers Active TSS ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	40 gene(s)	inside rSNPs	diseases
4	nsv516233	chr3:121419301-121670405	Weak transcription Flanking Active TSS Strong transcription ZNF genes & repeats Enhancers Genic enhancers Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	37 gene(s)	inside rSNPs	diseases
5	nsv877383	chr3:121465220-121650736	Strong transcription Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	35 gene(s)	inside rSNPs	diseases
6	nsv432483	chr3:121488995-121629634	Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
7	esv33139	chr3:121500400-122091831	Strong transcription Weak transcription Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Active TSS Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	21 gene(s)	inside rSNPs	diseases
8	nsv877384	chr3:121601577-121659774	Strong transcription Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs1881998	PARP14	cis	cerebellum	SCAN

Chromatin state (count:59 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:121555800-121615600	Weak transcription	Primary T cells from cord blood	blood
2	chr3:121592800-121646800	Weak transcription	Rectal Mucosa Donor 29	rectum
3	chr3:121593000-121615400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
4	chr3:121593000-121632400	Weak transcription	Duodenum Mucosa	Duodenum
5	chr3:121610600-121621800	Strong transcription	Monocytes-CD14+_RO01746	blood
6	chr3:121612200-121614200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
7	chr3:121612400-121616000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
8	chr3:121612800-121614800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
9	chr3:121612800-121615000	Active TSS	Fetal Muscle Trunk	muscle
10	chr3:121613000-121614200	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
11	chr3:121613000-121614200	Flanking Active TSS	HUES64 Cell Line	embryonic stem cell
12	chr3:121613000-121614200	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell
13	chr3:121613000-121614200	Active TSS	Brain Anterior Caudate	brain
14	chr3:121613000-121614200	Active TSS	Brain Cingulate Gyrus	brain
15	chr3:121613000-121614200	Enhancers	Fetal Heart	heart
16	chr3:121613000-121614200	Enhancers	Fetal Lung	lung
17	chr3:121613000-121614200	Enhancers	Skeletal Muscle Male	skeletal muscle
18	chr3:121613000-121615000	Enhancers	H9 Cell Line	embryonic stem cell
19	chr3:121613000-121615200	Enhancers	Breast Myoepithelial Primary Cells	Breast
20	chr3:121613000-121615600	Enhancers	Skeletal Muscle Female	skeletal muscle
21	chr3:121613000-121616600	Strong transcription	Primary hematopoietic stem cells short term culture	blood
22	chr3:121613000-121616800	Strong transcription	GM12878-XiMat	blood
23	chr3:121613000-121620600	Strong transcription	Primary B cells from cord blood	blood
24	chr3:121613000-121621800	Strong transcription	Primary B cells from peripheral blood	blood
25	chr3:121613000-121622000	Strong transcription	Primary monocytes fromperipheralblood	blood
26	chr3:121613200-121614400	Flanking Active TSS	Cortex derived primary cultured neurospheres	brain
27	chr3:121613200-121619400	Strong transcription	Primary hematopoietic stem cells	blood
28	chr3:121613400-121614200	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
29	chr3:121613400-121614200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
30	chr3:121613400-121614200	Enhancers	Brain Germinal Matrix	brain
31	chr3:121613400-121614800	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
32	chr3:121613400-121615400	Weak transcription	Pancreas	Pancrea
33	chr3:121613400-121622000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
34	chr3:121613400-121626400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
35	chr3:121613600-121614200	Enhancers	Brain Angular Gyrus	brain
36	chr3:121613600-121614200	Active TSS	Brain Substantia Nigra	brain
37	chr3:121613600-121614600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
38	chr3:121613600-121614600	Weak transcription	Psoas Muscle	Psoas
39	chr3:121613600-121614800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
40	chr3:121613600-121614800	Weak transcription	Placenta Amnion	Placenta Amnion
41	chr3:121613600-121615200	Enhancers	iPS-15b Cell Line	embryonic stem cell
42	chr3:121613600-121617400	Weak transcription	Aorta	Aorta
43	chr3:121613800-121614200	Enhancers	ES-I3 Cell Line	embryonic stem cell
44	chr3:121613800-121614200	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
45	chr3:121613800-121614200	Enhancers	Adipose Nuclei	Adipose
46	chr3:121613800-121614200	Enhancers	Liver	Liver
47	chr3:121613800-121614800	Enhancers	ES-WA7 Cell Line	embryonic stem cell
48	chr3:121613800-121614800	Weak transcription	Placenta	Placenta
49	chr3:121613800-121615000	Enhancers	Primary neutrophils fromperipheralblood	blood
50	chr3:121613800-121615000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin

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