Variant report

Variant	rs6781311
Chromosome Location	chr3:195145704-195145705
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr3:195138714..195141452-chr3:195144940..195147582,4	K562	blood:
2	chr3:195145080..195147347-chr3:195150908..195152978,2	K562	blood:
3	chr3:195145480..195148513-chr3:195161599..195165057,3	K562	blood:

Variant related genes	Relation type
ENSG00000114331	Chromatin interaction
ENSG00000207368	Chromatin interaction

Extended variants
information (count: 156 )
Associated
traits (count: 2 )

rSNPs within LD-proxies of this variant (count:133)

rs_ID	r²[population]
rs10439946	0.85[AFR][1000 genomes];0.85[EUR][1000 genomes]
rs10439947	0.85[AFR][1000 genomes];0.85[EUR][1000 genomes]
rs10439948	0.82[AFR][1000 genomes];0.85[EUR][1000 genomes]
rs10439949	0.85[AFR][1000 genomes];0.85[EUR][1000 genomes]
rs11706218	0.86[EUR][1000 genomes]
rs11718226	0.86[EUR][1000 genomes]
rs12054139	0.86[EUR][1000 genomes]
rs12054333	0.83[EUR][1000 genomes]
rs12054406	0.84[EUR][1000 genomes]
rs12629884	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12630009	0.84[EUR][1000 genomes]
rs13316914	0.92[EUR][1000 genomes]
rs13317705	0.85[EUR][1000 genomes]
rs13317782	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs13320698	0.92[AMR][1000 genomes];0.91[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs13325966	0.85[EUR][1000 genomes]
rs1353133	0.86[AFR][1000 genomes];0.95[AMR][1000 genomes];0.95[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1538768	0.85[EUR][1000 genomes]
rs1826584	0.87[EUR][1000 genomes]
rs1890853	0.83[AFR][1000 genomes];0.95[AMR][1000 genomes];0.93[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs1994880	0.87[EUR][1000 genomes]
rs1994881	0.82[AFR][1000 genomes];0.87[EUR][1000 genomes]
rs2000052	0.81[AMR][1000 genomes]
rs2029708	0.91[AFR][1000 genomes];0.98[AMR][1000 genomes];0.95[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2050806	0.98[AMR][1000 genomes];0.93[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs2066154	0.84[EUR][1000 genomes]
rs2131685	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs2275518	0.86[EUR][1000 genomes]
rs2410792	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs4677668	0.84[EUR][1000 genomes]
rs4677669	0.86[EUR][1000 genomes]
rs4677826	0.86[EUR][1000 genomes]
rs4677827	0.86[EUR][1000 genomes]
rs4677828	0.95[AMR][1000 genomes];0.93[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs4677829	0.85[EUR][1000 genomes]
rs4677832	0.85[AFR][1000 genomes];0.85[EUR][1000 genomes]
rs4677833	0.86[EUR][1000 genomes]
rs4677837	0.87[EUR][1000 genomes]
rs4677838	0.87[EUR][1000 genomes]
rs4677839	0.85[AFR][1000 genomes];0.95[AMR][1000 genomes];0.95[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs4677840	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs4677842	0.87[EUR][1000 genomes]
rs4677843	0.87[EUR][1000 genomes]
rs4677844	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs57760978	0.86[EUR][1000 genomes]
rs58067895	0.83[AFR][1000 genomes];0.98[AMR][1000 genomes];0.95[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs58178384	0.82[AFR][1000 genomes];0.87[EUR][1000 genomes]
rs59004692	0.87[AFR][1000 genomes];0.92[EUR][1000 genomes]
rs59551685	0.85[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs60100329	0.86[EUR][1000 genomes]
rs60177727	0.85[EUR][1000 genomes]
rs62287069	0.84[EUR][1000 genomes]
rs62287106	0.84[EUR][1000 genomes]
rs62287107	0.86[EUR][1000 genomes]
rs62287108	0.86[EUR][1000 genomes]
rs62287109	0.83[EUR][1000 genomes]
rs62287111	0.85[EUR][1000 genomes]
rs62287119	0.86[EUR][1000 genomes]
rs62288360	0.81[AFR][1000 genomes];0.85[EUR][1000 genomes]
rs62288364	0.87[EUR][1000 genomes]
rs62288365	0.87[EUR][1000 genomes]
rs62288367	0.86[EUR][1000 genomes]
rs62288369	0.87[EUR][1000 genomes]
rs62288441	0.92[EUR][1000 genomes]
rs62288442	0.90[EUR][1000 genomes]
rs6437373	0.84[EUR][1000 genomes]
rs6437375	0.85[AFR][1000 genomes];0.85[EUR][1000 genomes]
rs6437376	0.85[AFR][1000 genomes];0.95[AMR][1000 genomes];0.93[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs6437471	0.86[EUR][1000 genomes]
rs6763335	0.86[EUR][1000 genomes]
rs6763588	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs6771771	0.85[EUR][1000 genomes]
rs6778652	0.92[EUR][1000 genomes]
rs6785382	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs6788868	0.92[EUR][1000 genomes]
rs6791563	0.92[EUR][1000 genomes]
rs6794216	0.85[EUR][1000 genomes]
rs6800221	0.85[AFR][1000 genomes];0.90[EUR][1000 genomes]
rs6800562	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs6801007	0.87[EUR][1000 genomes]
rs6801315	0.85[EUR][1000 genomes]
rs6801750	0.85[AFR][1000 genomes];0.98[AMR][1000 genomes];0.95[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs6803477	0.88[AFR][1000 genomes];0.89[EUR][1000 genomes]
rs6803763	0.83[AFR][1000 genomes];0.86[EUR][1000 genomes]
rs6806850	0.85[AFR][1000 genomes];0.86[EUR][1000 genomes]
rs716898	0.98[AMR][1000 genomes];0.92[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs73208931	0.90[EUR][1000 genomes]
rs7430205	0.86[EUR][1000 genomes]
rs7611090	0.81[EUR][1000 genomes]
rs7616598	0.87[EUR][1000 genomes]
rs7617936	0.98[AMR][1000 genomes];0.92[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs7618499	0.86[EUR][1000 genomes]
rs7621133	0.83[AFR][1000 genomes];0.87[EUR][1000 genomes]
rs7623135	0.83[AFR][1000 genomes];0.95[AMR][1000 genomes];0.93[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs7627054	0.86[EUR][1000 genomes]
rs7627671	0.83[AFR][1000 genomes];0.98[AMR][1000 genomes];0.93[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs7635603	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7635906	0.85[EUR][1000 genomes]
rs7636824	0.84[EUR][1000 genomes]
rs7639146	0.83[AFR][1000 genomes];0.86[EUR][1000 genomes]
rs7641810	0.86[EUR][1000 genomes]
rs7650623	0.85[AFR][1000 genomes];0.85[EUR][1000 genomes]
rs7652612	0.82[EUR][1000 genomes]
rs7653406	0.84[EUR][1000 genomes]
rs9288744	0.98[AMR][1000 genomes];0.93[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs9288746	0.91[AFR][1000 genomes];0.98[AMR][1000 genomes];0.97[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs9681021	0.98[AMR][1000 genomes];0.94[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs9809730	0.86[EUR][1000 genomes]
rs9812506	0.98[AMR][1000 genomes];0.92[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs9813425	0.90[AFR][1000 genomes];0.95[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs9814214	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs9814344	0.86[EUR][1000 genomes]
rs9817672	0.87[EUR][1000 genomes]
rs9821765	0.87[AFR][1000 genomes];0.92[EUR][1000 genomes]
rs9826999	0.81[AFR][1000 genomes];0.87[EUR][1000 genomes]
rs9836665	0.87[EUR][1000 genomes]
rs9844354	0.98[AMR][1000 genomes];0.92[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs9846555	0.86[EUR][1000 genomes]
rs9847544	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs9848201	0.87[EUR][1000 genomes]
rs9848473	0.86[EUR][1000 genomes]
rs9854941	0.85[EUR][1000 genomes]
rs9855453	0.85[EUR][1000 genomes]
rs9859279	0.95[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs9859902	0.84[EUR][1000 genomes]
rs9860798	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs9862710	0.84[EUR][1000 genomes]
rs9864603	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs9866537	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs9868768	0.80[AFR][1000 genomes];0.94[AMR][1000 genomes];0.93[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs9870236	0.87[EUR][1000 genomes]
rs9876967	0.90[EUR][1000 genomes]
rs9879305	0.85[EUR][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	nsv1014826	chr3:194834615-195631793	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	73 gene(s)	inside rSNPs	diseases
2	nsv536876	chr3:194834615-195631793	Strong transcription Flanking Active TSS Weak transcription Enhancers Active TSS ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	73 gene(s)	inside rSNPs	diseases
3	nsv533904	chr3:194868329-195438728	Enhancers Weak transcription Flanking Active TSS Strong transcription Genic enhancers Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	65 gene(s)	inside rSNPs	diseases
4	esv1832781	chr3:194902818-195528226	Strong transcription Enhancers Weak transcription Flanking Active TSS Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	62 gene(s)	inside rSNPs	diseases
5	nsv432508	chr3:194916131-195478861	Strong transcription Enhancers Weak transcription Genic enhancers Active TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	59 gene(s)	inside rSNPs	diseases
6	nsv432510	chr3:194935314-195478861	Weak transcription Enhancers Strong transcription Active TSS Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	59 gene(s)	inside rSNPs	diseases
7	nsv1005519	chr3:194964301-195340515	Active TSS Flanking Active TSS Weak transcription Enhancers Bivalent Enhancer Strong transcription ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	41 gene(s)	inside rSNPs	diseases
8	nsv432511	chr3:194986167-195479748	Weak transcription Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Genic enhancers Active TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	57 gene(s)	inside rSNPs	diseases
9	nsv432512	chr3:195007260-195475989	Enhancers Weak transcription Active TSS Genic enhancers Strong transcription ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	54 gene(s)	inside rSNPs	diseases
10	nsv878138	chr3:195057001-195477791	Enhancers Active TSS Genic enhancers Flanking Active TSS Strong transcription Weak transcription Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	53 gene(s)	inside rSNPs	diseases
11	nsv878139	chr3:195058837-195158031	Enhancers Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
12	esv1799680	chr3:195060129-195154361	Enhancers Weak transcription Flanking Active TSS Genic enhancers Strong transcription ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	n/a
13	nsv878141	chr3:195065255-195158031	Enhancers Weak transcription Strong transcription ZNF genes & repeats Flanking Active TSS Genic enhancers Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
14	nsv1006229	chr3:195071421-195474751	Weak transcription Flanking Active TSS Active TSS Genic enhancers Enhancers Strong transcription ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	53 gene(s)	inside rSNPs	diseases
15	esv2754364	chr3:195102703-195553690	Enhancers Weak transcription Genic enhancers Bivalent Enhancer Active TSS Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	54 gene(s)	inside rSNPs	diseases
16	esv2757028	chr3:195102787-195479748	Active TSS Enhancers Strong transcription Flanking Active TSS Bivalent Enhancer Weak transcription Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	53 gene(s)	inside rSNPs	diseases
17	esv2759213	chr3:195102787-196071593	Active TSS Weak transcription Flanking Active TSS Strong transcription Enhancers Bivalent Enhancer Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	144 gene(s)	inside rSNPs	diseases
18	nsv878143	chr3:195115229-195158031	Weak transcription Enhancers ZNF genes & repeats Strong transcription Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
19	nsv878144	chr3:195120090-195158031	Weak transcription Enhancers Strong transcription Genic enhancers ZNF genes & repeats Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
20	nsv432513	chr3:195121072-195478861	Strong transcription Weak transcription Active TSS Enhancers Bivalent Enhancer Genic enhancers Flanking Active TSS 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	52 gene(s)	inside rSNPs	diseases
21	nsv432514	chr3:195121110-195478861	Bivalent Enhancer Weak transcription Flanking Active TSS Enhancers Active TSS Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	52 gene(s)	inside rSNPs	diseases
22	nsv432515	chr3:195121110-195528226	Weak transcription Enhancers Strong transcription Bivalent Enhancer ZNF genes & repeats Genic enhancers 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	54 gene(s)	inside rSNPs	diseases
23	nsv829824	chr3:195131067-195286698	Weak transcription Active TSS Strong transcription Genic enhancers Enhancers Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	30 gene(s)	inside rSNPs	diseases

mRNA abundance (count:2)

SNP	Gene	Cis/trans	Tissue	Source
rs6781311	XXYLT1	cis	Esophagus Mucosa	GTEx
rs6781311	XXYLT1	cis	Skin Sun Exposed Lower leg	GTEx

Chromatin state (count:49 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:195088600-195146800	Weak transcription	Spleen	Spleen
2	chr3:195094800-195161200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
3	chr3:195095200-195161800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
4	chr3:195116400-195147600	Weak transcription	Fetal Intestine Small	intestine
5	chr3:195123800-195146400	Weak transcription	Pancreatic Islets	Pancreatic Islet
6	chr3:195125000-195147600	Weak transcription	Left Ventricle	heart
7	chr3:195127000-195149800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
8	chr3:195131600-195146800	Weak transcription	Primary B cells from peripheral blood	blood
9	chr3:195131800-195154800	Weak transcription	Cortex derived primary cultured neurospheres	brain
10	chr3:195131800-195160600	Weak transcription	Hela-S3	cervix
11	chr3:195132000-195148000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
12	chr3:195132000-195161200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
13	chr3:195132200-195147800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
14	chr3:195132600-195147800	Weak transcription	Primary B cells from cord blood	blood
15	chr3:195133000-195146000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
16	chr3:195133800-195161000	Weak transcription	NHDF-Ad	bronchial
17	chr3:195138200-195146800	Weak transcription	NHEK	skin
18	chr3:195138400-195146600	Weak transcription	Thymus	Thymus
19	chr3:195138600-195146800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
20	chr3:195138600-195157200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
21	chr3:195139200-195146000	Weak transcription	Primary T cells from cord blood	blood
22	chr3:195139200-195146200	Weak transcription	Primary hematopoietic stem cells	blood
23	chr3:195139400-195146200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
24	chr3:195140000-195146600	Weak transcription	Ovary	ovary
25	chr3:195140200-195146600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
26	chr3:195140200-195146600	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
27	chr3:195140600-195146200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
28	chr3:195141200-195146600	Weak transcription	Primary monocytes fromperipheralblood	blood
29	chr3:195142400-195146800	Weak transcription	Brain Substantia Nigra	brain
30	chr3:195142600-195146200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
31	chr3:195143000-195146200	Weak transcription	Primary neutrophils fromperipheralblood	blood
32	chr3:195143000-195146800	Weak transcription	Brain Inferior Temporal Lobe	brain
33	chr3:195143600-195146600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
34	chr3:195143600-195149200	Weak transcription	Aorta	Aorta
35	chr3:195143800-195146400	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
36	chr3:195144200-195146200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
37	chr3:195144400-195146800	Weak transcription	Right Atrium	heart
38	chr3:195144400-195149800	Weak transcription	Psoas Muscle	Psoas
39	chr3:195144600-195146200	Weak transcription	Primary T helper cells fromperipheralblood	blood
40	chr3:195144600-195146600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
41	chr3:195144800-195145800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
42	chr3:195144800-195146600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
43	chr3:195144800-195161200	Weak transcription	Sigmoid Colon	Sigmoid Colon
44	chr3:195145000-195146800	Weak transcription	HSMM	muscle
45	chr3:195145000-195155000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
46	chr3:195145200-195148200	Enhancers	Primary T helper cells PMA-I stimulated	--
47	chr3:195145400-195154600	Weak transcription	Primary T cells fromperipheralblood	blood
48	chr3:195145600-195145800	Enhancers	Adipose Nuclei	Adipose
49	chr3:195145600-195162400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links