Variant report

Variant	rs12673450
Chromosome Location	chr7:66009220-66009221
allele	A/G
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	POLR2A	chr7:66007626-66009542	K562	blood:	n/a	n/a
2	POLR2A	chr7:66008872-66009487	K562	blood:	n/a	n/a

Variant related genes	Relation type
ENSG00000229180	TF binding region

Extended variants
information (count: 149 )
Associated
traits (count: 21 )

rSNPs within LD-proxies of this variant (count:138)

rs_ID	r²[population]
rs10107	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.91[AFR][1000 genomes];0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10233806	0.89[CEU][hapmap];0.94[YRI][hapmap]
rs10244498	0.89[CEU][hapmap];0.83[CHB][hapmap];0.94[YRI][hapmap]
rs10265311	0.88[AMR][1000 genomes];0.88[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs10271548	0.84[ASN][1000 genomes]
rs10274883	0.90[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs10278014	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.84[AFR][1000 genomes];0.86[AMR][1000 genomes];0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10281499	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs10807704	0.83[AFR][1000 genomes]
rs10950043	0.86[AFR][1000 genomes];0.93[AMR][1000 genomes];0.95[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs10950046	0.83[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs11761542	0.86[EUR][1000 genomes]
rs11763189	0.85[AFR][1000 genomes];0.80[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs11765791	0.80[AFR][1000 genomes];0.84[AMR][1000 genomes];0.86[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs11765965	0.83[CEU][hapmap]
rs11769079	0.93[YRI][hapmap]
rs11772819	0.86[EUR][1000 genomes]
rs11772884	0.85[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs11773628	0.83[AFR][1000 genomes];0.80[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs12333370	0.92[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs12532998	0.89[CEU][hapmap]
rs12668005	0.83[AFR][1000 genomes];0.84[AMR][1000 genomes];0.81[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs12698520	0.88[CEU][hapmap]
rs12698522	0.83[AFR][1000 genomes];0.92[AMR][1000 genomes];0.87[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs12698526	0.83[AFR][1000 genomes];0.92[AMR][1000 genomes];0.88[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs13226170	0.93[AFR][1000 genomes];0.93[AMR][1000 genomes];0.96[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs13232191	0.88[AFR][1000 genomes];0.93[AMR][1000 genomes];0.95[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs13240501	0.88[AFR][1000 genomes];0.86[AMR][1000 genomes];0.93[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs13242290	0.90[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs13308803	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.87[EUR][1000 genomes]
rs13536	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.91[AFR][1000 genomes];0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1638735	0.81[YRI][hapmap]
rs1695820	1.00[CEU][hapmap];0.95[YRI][hapmap]
rs17747530	0.92[AFR][1000 genomes];0.93[AMR][1000 genomes];0.94[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1860469	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.92[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs1860472	0.92[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1968126	0.84[AMR][1000 genomes];0.90[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1968225	0.89[CEU][hapmap]
rs2003300	0.94[YRI][hapmap]
rs2013908	1.00[CEU][hapmap];0.96[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.90[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs2024192	0.86[AFR][1000 genomes];0.86[AMR][1000 genomes];0.94[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2077593	0.89[CEU][hapmap]
rs2109295	0.81[AFR][1000 genomes];0.88[AMR][1000 genomes];0.92[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs2109297	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.90[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs2420608	0.81[AFR][1000 genomes];0.82[EUR][1000 genomes]
rs2420610	0.95[AFR][1000 genomes];0.93[AMR][1000 genomes];0.95[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2420611	0.93[AFR][1000 genomes];0.93[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2659890	0.87[EUR][1000 genomes]
rs2659891	0.87[EUR][1000 genomes]
rs2659892	0.96[CEU][hapmap];0.87[EUR][1000 genomes]
rs2659893	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.87[EUR][1000 genomes]
rs2659896	0.85[EUR][1000 genomes]
rs2659898	0.87[EUR][1000 genomes]
rs2659901	0.87[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs2659907	0.89[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs2659908	0.89[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs2707824	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.87[EUR][1000 genomes]
rs2707837	0.86[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs2707847	0.87[EUR][1000 genomes]
rs2707851	0.81[YRI][hapmap]
rs28431318	0.81[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs28480509	0.91[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs28617601	0.83[AMR][1000 genomes];0.83[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs28714531	0.83[AFR][1000 genomes];0.93[AMR][1000 genomes];0.88[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs28731376	0.88[AFR][1000 genomes];0.89[AMR][1000 genomes];0.93[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2901209	0.83[AFR][1000 genomes];0.90[EUR][1000 genomes]
rs35378740	0.88[AFR][1000 genomes];0.93[AMR][1000 genomes];0.95[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs3735148	0.89[CEU][hapmap]
rs3846973	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.90[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs3857685	0.80[AFR][1000 genomes];0.86[AMR][1000 genomes];0.86[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs3926380	0.81[AFR][1000 genomes];0.81[AMR][1000 genomes];0.92[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs4506088	0.85[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs4717315	0.87[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs4718377	0.84[AFR][1000 genomes];0.86[AMR][1000 genomes];0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4718383	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.90[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs57739047	0.82[AFR][1000 genomes];0.80[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs58347342	0.86[EUR][1000 genomes]
rs61348003	0.84[AFR][1000 genomes];0.88[AMR][1000 genomes];0.95[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs6460292	0.89[CEU][hapmap]
rs6460293	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.89[YRI][hapmap]
rs6460296	0.89[CEU][hapmap]
rs6460301	0.83[AFR][1000 genomes]
rs6460302	1.00[CEU][hapmap];0.95[YRI][hapmap];0.83[AFR][1000 genomes];0.83[EUR][1000 genomes]
rs6460303	0.83[AFR][1000 genomes];0.93[AMR][1000 genomes];0.88[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs6460304	1.00[CEU][hapmap];0.95[YRI][hapmap];0.83[AFR][1000 genomes];0.80[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs6460307	1.00[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs66981195	0.81[AMR][1000 genomes];0.91[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs6945019	0.89[CEU][hapmap]
rs6945032	0.89[CEU][hapmap]
rs6945775	0.83[AFR][1000 genomes]
rs6947339	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[YRI][hapmap]
rs6950137	1.00[CEU][hapmap];1.00[YRI][hapmap]
rs6951302	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.89[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs6951946	0.81[AFR][1000 genomes];0.86[AMR][1000 genomes];0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs6955837	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.86[AFR][1000 genomes];0.86[AMR][1000 genomes];0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs6958200	0.81[AFR][1000 genomes]
rs6959268	1.00[CEU][hapmap];0.83[YRI][hapmap]
rs6962717	1.00[CEU][hapmap];0.95[YRI][hapmap]
rs6963228	0.82[ASN][1000 genomes]
rs6971059	0.80[AFR][1000 genomes];0.86[AMR][1000 genomes];0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs6973249	0.81[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs6976714	0.88[YRI][hapmap];0.81[AFR][1000 genomes]
rs6978028	0.85[ASN][1000 genomes]
rs6978178	0.90[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs6980451	0.83[EUR][1000 genomes]
rs709595	0.89[CEU][hapmap]
rs721717	0.84[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs7384021	0.80[AMR][1000 genomes];0.91[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7385102	0.81[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs7778322	0.83[AFR][1000 genomes]
rs7782587	0.88[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs778697	1.00[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];0.94[YRI][hapmap]
rs778702	1.00[CEU][hapmap]
rs778706	0.89[CEU][hapmap]
rs778711	1.00[CEU][hapmap];0.95[YRI][hapmap]
rs778720	1.00[CEU][hapmap];1.00[YRI][hapmap]
rs778722	0.92[CEU][hapmap]
rs778734	1.00[CEU][hapmap];0.85[YRI][hapmap]
rs778736	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[YRI][hapmap]
rs7789615	0.82[ASN][1000 genomes]
rs7789768	0.89[CEU][hapmap]
rs7792762	0.85[AFR][1000 genomes]
rs7793723	0.83[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7800620	0.86[EUR][1000 genomes]
rs7805152	0.85[EUR][1000 genomes]
rs7808013	0.80[AMR][1000 genomes];0.92[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs801194	0.87[AFR][1000 genomes];0.86[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs801195	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.89[AFR][1000 genomes];0.90[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs801202	0.91[AFR][1000 genomes];0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs801203	0.91[AFR][1000 genomes];0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs801204	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.83[AFR][1000 genomes];0.92[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs801206	0.91[AFR][1000 genomes];0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs801208	0.89[AFR][1000 genomes];0.90[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs801209	0.91[AFR][1000 genomes];0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs801215	0.81[AFR][1000 genomes];0.89[AMR][1000 genomes];0.88[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs881285	0.89[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs9791712	0.92[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs9791713	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.92[EUR][1000 genomes];0.90[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:11 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv532124	chr7:65371521-66234730	Enhancers Strong transcription Active TSS Weak transcription Flanking Active TSS Genic enhancers ZNF genes & repeats 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	125 gene(s)	inside rSNPs	diseases
2	nsv1026559	chr7:65617368-66370805	Weak transcription Enhancers Flanking Active TSS Strong transcription Active TSS ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	116 gene(s)	inside rSNPs	diseases
3	nsv1035107	chr7:65814901-66114919	Genic enhancers Strong transcription ZNF genes & repeats Enhancers Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	69 gene(s)	inside rSNPs	diseases
4	nsv538909	chr7:65814901-66114919	Strong transcription Weak transcription Bivalent Enhancer Active TSS Enhancers Flanking Active TSS Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	69 gene(s)	inside rSNPs	diseases
5	nsv888326	chr7:65825257-66066999	Weak transcription Flanking Active TSS Strong transcription Enhancers Genic enhancers Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	41 gene(s)	inside rSNPs	diseases
6	nsv482441	chr7:65885824-66061788	Strong transcription Weak transcription Enhancers Genic enhancers Flanking Active TSS Bivalent/Poised TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	37 gene(s)	inside rSNPs	diseases
7	esv3447484	chr7:65909457-66033145	Weak transcription Flanking Active TSS Strong transcription Enhancers Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	29 gene(s)	inside rSNPs	diseases
8	esv3377926	chr7:65934493-66051484	Strong transcription Weak transcription Active TSS Flanking Active TSS Enhancers Genic enhancers Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	30 gene(s)	inside rSNPs	diseases
9	nsv888327	chr7:65938980-66029429	Active TSS Strong transcription Weak transcription Flanking Active TSS Enhancers Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	29 gene(s)	inside rSNPs	diseases
10	esv3423847	chr7:65941210-66054107	Flanking Active TSS Weak transcription Strong transcription Active TSS Enhancers Genic enhancers Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	29 gene(s)	inside rSNPs	diseases
11	nsv967444	chr7:65992587-66013934	Strong transcription Weak transcription Enhancers Genic enhancers Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

mRNA abundance (count:21)

SNP	Gene	Cis/trans	Tissue	Source
rs12673450	GS1-124K5.4	cis	Stomach	GTEx
rs12673450	GS1-124K5.4	cis	Skin Sun Exposed Lower leg	GTEx
rs12673450	RP4-756H11.3	cis	Nerve Tibial	GTEx
rs12673450	GS1-124K5.4	cis	Esophagus Mucosa	GTEx
rs12673450	RP4-756H11.3	cis	Artery Tibial	GTEx
rs12673450	RP4-756H11.3	cis	Adipose Subcutaneous	GTEx
rs12673450	LINC00174	cis	Thyroid	GTEx
rs12673450	RP4-756H11.3	cis	Heart Left Ventricle	GTEx
rs12673450	RP4-756H11.3	cis	Muscle Skeletal	GTEx
rs12673450	GS1-124K5.2	cis	Whole Blood	GTEx
rs12673450	RP4-756H11.3	cis	Thyroid	GTEx
rs12673450	ASL	Cis_1M	lymphoblastoid	RTeQTL
rs12673450	GS1-124K5.11	cis	Thyroid	GTEx
rs12673450	RP4-756H11.3	cis	Esophagus Mucosa	GTEx
rs12673450	LOC493754	cis	normal skin	skin_eQTL
rs12673450	RP4-756H11.3	cis	lung	GTEx
rs12673450	RP4-756H11.3	cis	Skin Sun Exposed Lower leg	GTEx
rs12673450	GS1-124K5.4	cis	Artery Aorta	GTEx
rs12673450	GTF2IRD1P1	cis	Thyroid	GTEx
rs12673450	RNU6-96P	cis	Thyroid	GTEx
rs12673450	RP4-756H11.3	cis	Esophagus Muscularis	GTEx

Chromatin state (count:124 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:65991200-66009800	Weak transcription	Small Intestine	intestine
2	chr7:65993600-66009400	Weak transcription	HSMM	muscle
3	chr7:65994000-66014400	Weak transcription	Colon Smooth Muscle	Colon
4	chr7:65995000-66010000	Weak transcription	Fetal Lung	lung
5	chr7:65995000-66017200	Weak transcription	Primary hematopoietic stem cells	blood
6	chr7:65999800-66022400	Strong transcription	Fetal Stomach	stomach
7	chr7:66000600-66019200	Weak transcription	Fetal Kidney	kidney
8	chr7:66000800-66016600	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
9	chr7:66001200-66014400	Weak transcription	A549	lung
10	chr7:66001400-66022400	Weak transcription	Stomach Mucosa	stomach
11	chr7:66002800-66016000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
12	chr7:66003600-66018800	Weak transcription	GM12878-XiMat	blood
13	chr7:66003800-66022200	Strong transcription	Stomach Smooth Muscle	stomach
14	chr7:66003800-66022800	Strong transcription	Fetal Intestine Small	intestine
15	chr7:66004200-66010000	Weak transcription	H1 Cell Line	embryonic stem cell
16	chr7:66004200-66012400	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
17	chr7:66004400-66010400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
18	chr7:66004400-66011000	Strong transcription	Spleen	Spleen
19	chr7:66004400-66052600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
20	chr7:66004600-66016600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
21	chr7:66004800-66015400	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
22	chr7:66004800-66019200	Weak transcription	HUVEC	blood vessel
23	chr7:66004800-66037200	Weak transcription	Psoas Muscle	Psoas
24	chr7:66005000-66010000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
25	chr7:66005000-66014400	Weak transcription	HUES48 Cell Line	embryonic stem cell
26	chr7:66005000-66016800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
27	chr7:66005200-66016600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
28	chr7:66005200-66022400	Strong transcription	Fetal Muscle Trunk	muscle
29	chr7:66005800-66016800	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
30	chr7:66006000-66020000	Strong transcription	Sigmoid Colon	Sigmoid Colon
31	chr7:66006000-66022200	Strong transcription	Breast Myoepithelial Primary Cells	Breast
32	chr7:66006200-66010200	Strong transcription	Right Ventricle	heart
33	chr7:66006200-66010800	Strong transcription	Fetal Brain Female	brain
34	chr7:66006200-66010800	Strong transcription	Gastric	stomach
35	chr7:66006200-66010800	Strong transcription	Skeletal Muscle Female	skeletal muscle
36	chr7:66006200-66011000	Strong transcription	Primary neutrophils fromperipheralblood	blood
37	chr7:66006200-66011000	Strong transcription	Primary T cells from cord blood	blood
38	chr7:66006200-66011000	Strong transcription	Placenta	Placenta
39	chr7:66006200-66011600	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
40	chr7:66006200-66011800	Strong transcription	Pancreas	Pancrea
41	chr7:66006200-66011800	Strong transcription	Dnd41	blood
42	chr7:66006200-66013800	Strong transcription	Duodenum Smooth Muscle	Duodenum
43	chr7:66006200-66019400	Strong transcription	Adipose Nuclei	Adipose
44	chr7:66006200-66021000	Strong transcription	Fetal Intestine Large	intestine
45	chr7:66006200-66022200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
46	chr7:66006200-66022400	Strong transcription	Lung	lung
47	chr7:66006200-66022600	Strong transcription	Cortex derived primary cultured neurospheres	brain
48	chr7:66006200-66024400	Strong transcription	Fetal Muscle Leg	muscle
49	chr7:66006200-66024400	Strong transcription	Thymus	Thymus
50	chr7:66006400-66022800	Strong transcription	Brain Germinal Matrix	brain

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