Variant report

Variant	rs3758076
Chromosome Location	chr8:86375535-86375536
allele	C/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	CTCF	chr8:86375500-86375650	SK-N-SH_RA	brain:	n/a	chr8:86375565-86375578
2	CTCF	chr8:86375480-86375630	GM12865	blood:	n/a	chr8:86375565-86375578
3	POLR2A	chr8:86375317-86376565	HL-60	blood:	n/a	n/a
4	RAD21	chr8:86375302-86375777	HepG2	liver:	n/a	chr8:86375566-86375579
5	RAD21	chr8:86375431-86375637	K562	blood:	n/a	chr8:86375566-86375579
6	SMC3	chr8:86375371-86375759	K562	blood:	n/a	chr8:86375564-86375578
7	CTCF	chr8:86375500-86375650	HPAF	blood vessel:	n/a	chr8:86375565-86375578
8	RAD21	chr8:86375421-86375787	H1-hESC	embryonic stem cell:	n/a	chr8:86375566-86375579
9	CTCF	chr8:86375500-86375650	Hela-S3	cervix:	n/a	chr8:86375565-86375578
10	CTCF	chr8:86375403-86375736	GM19238	blood:	n/a	chr8:86375565-86375578
11	MAX	chr8:86375479-86375665	K562	blood:	n/a	n/a
12	GTF2F1	chr8:86375439-86375703	H1-hESC	embryonic stem cell:	n/a	n/a
13	YY1	chr8:86375426-86375701	GM12878	blood:	n/a	chr8:86375605-86375616
14	UBTF	chr8:86375474-86375638	K562	blood:	n/a	n/a
15	CTCF	chr8:86375520-86375670	GM12870	blood:	n/a	chr8:86375565-86375578
16	CTCF	chr8:86375500-86375650	HRE	kidney:	n/a	chr8:86375565-86375578
17	RAD21	chr8:86375365-86375895	H1-hESC	embryonic stem cell:	n/a	chr8:86375566-86375579
18	CTCF	chr8:86375460-86375610	NB4	blood:	n/a	chr8:86375565-86375578
19	CTCF	chr8:86375500-86375650	AG09319	gingival:	n/a	chr8:86375565-86375578
20	ZNF143	chr8:86375397-86375736	K562	blood:	n/a	chr8:86375718-86375728 chr8:86375517-86375535
21	MYC	chr8:86375519-86375588	K562	blood:	n/a	n/a
22	ZNF143	chr8:86375425-86375644	Hela-S3	cervix:	n/a	chr8:86375517-86375535
23	CTCF	chr8:86375520-86375670	NHLF	lung:	n/a	chr8:86375565-86375578
24	CTCF	chr8:86375520-86375670	AoAF	blood vessel:	n/a	chr8:86375565-86375578
25	CTCF	chr8:86375406-86375732	K562	blood:	n/a	chr8:86375565-86375578
26	POLR2A	chr8:86375385-86376733	HL-60	blood:	n/a	n/a
27	CTCF	chr8:86375520-86375670	HCM	heart:	n/a	chr8:86375565-86375578
28	RFX5	chr8:86375487-86375736	Hela-S3	cervix:	n/a	n/a
29	CTCF	chr8:86375460-86375610	GM12878	blood:	n/a	chr8:86375565-86375578
30	CTCF	chr8:86375500-86375650	GM12871	blood:	n/a	chr8:86375565-86375578
31	CTCF	chr8:86375229-86375897	MCF-7	breast:	n/a	chr8:86375565-86375578
32	RAD21	chr8:86375407-86375743	SK-N-SH_RA	brain:	n/a	chr8:86375566-86375579
33	CTCF	chr8:86375500-86375650	HEEpiC	esophagus:	n/a	chr8:86375565-86375578
34	CTCF	chr8:86375520-86375670	HFF-Myc	foreskin:	n/a	chr8:86375565-86375578
35	E2F4	chr8:86375447-86375689	MCF10A-Er-Src	breast:	n/a	n/a
36	ATF2	chr8:86375277-86375647	GM12878	blood:	n/a	n/a
37	CTCF	chr8:86375480-86375630	AoAF	blood vessel:	n/a	chr8:86375565-86375578
38	POLR2A	chr8:86375441-86376677	GM18951	blood:	n/a	n/a
39	YY1	chr8:86375424-86375596	A549	lung:	n/a	n/a
40	CTCF	chr8:86375500-86375650	GM06990	blood:	n/a	chr8:86375565-86375578
41	MAX	chr8:86375515-86375654	HepG2	liver:	n/a	n/a
42	FOXM1	chr8:86375386-86375739	GM12878	blood:	n/a	n/a
43	CTCF	chr8:86375480-86375630	AG04450	lung:	n/a	chr8:86375565-86375578
44	CTCF	chr8:86375520-86375670	HUVEC	blood vessel:	n/a	chr8:86375565-86375578
45	CTCF	chr8:86375389-86375729	SK-N-SH_RA	brain:	n/a	chr8:86375565-86375578
46	CTCF	chr8:86375437-86375703	Hela-S3	cervix:	n/a	chr8:86375565-86375578
47	POLR2A	chr8:86375494-86376625	GM19099	blood:	n/a	n/a
48	POLR2A	chr8:86375490-86376505	GM18526	blood:	n/a	n/a
49	JUND	chr8:86375413-86375745	K562	blood:	n/a	chr8:86375591-86375598
50	MAX	chr8:86375367-86375963	MCF-7	breast:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:86375501-86375551	PANC-1	pancreas:	n/a
2	chr8:86375501-86375551	HAEpiC	amniotic membrane:	n/a
3	chr8:86375501-86375551	Caco-2	colon:	n/a
4	chr8:86375501-86375551	GM12878	blood:	n/a
5	chr8:86375501-86375551	HRCEpiC	kidney:	n/a
6	chr8:86375501-86375551	AG04449	skin:	fetal
7	chr8:86375501-86375551	GM19239	blood:	n/a
8	chr8:86375501-86375551	HEK293	kidney:	embryo
9	chr8:86375501-86375551	AG09319	gingival:	n/a
10	chr8:86375501-86375551	PFSK-1	brain:	n/a
11	chr8:86375501-86375551	CMK	blood:	n/a
12	chr8:86375501-86375551	NT2-D1	testis:	n/a
13	chr8:86375501-86375551	Hepatocyte	liver:	n/a
14	chr8:86375501-86375551	AG04450	lung:	fetal
15	chr8:86375501-86375551	AG09309	skin:	n/a
16	chr8:86375501-86375551	RPTEC	kidney:	n/a
17	chr8:86375501-86375551	HL-60	blood:	n/a
18	chr8:86375501-86375551	HepG2	liver:	n/a
19	chr8:86375501-86375551	HCM	heart:	n/a
20	chr8:86375501-86375551	GM12891	blood:	n/a
21	chr8:86375501-86375551	SK-N-SH_RA	brain:	n/a
22	chr8:86375501-86375551	T-47D	breast:	n/a
23	chr8:86375501-86375551	SK-N-MC	brain:	n/a
24	chr8:86375501-86375551	HIPEpiC	eye:	n/a
25	chr8:86375501-86375551	Jurkat	blood:	n/a
26	chr8:86375501-86375551	NH-A	brain:	n/a
27	chr8:86375501-86375551	NHBE	bronchial:	n/a
28	chr8:86375501-86375551	HNPCEpiC	eye:	n/a
29	chr8:86375501-86375551	ovcar-3	ovarian:	n/a
30	chr8:86375501-86375551	MCF-7	breast:	n/a
31	chr8:86375501-86375551	H1-hESC	embryonic stem cell:	embryo
32	chr8:86375501-86375551	NB4	blood:	n/a
33	chr8:86375501-86375551	HPAEpiC	pulmonary alveolar:	n/a
34	chr8:86375501-86375551	HMEC	breast:	n/a
35	chr8:86375501-86375551	K562	blood:	n/a
36	chr8:86375501-86375551	AG10803	skin:	n/a
37	chr8:86375501-86375551	HRE	kidney:	n/a
38	chr8:86375501-86375551	HEEpiC	esophagus:	n/a
39	chr8:86375501-86375551	BJ	skin:	n/a
40	chr8:86375501-86375551	HCF	heart:	n/a
41	chr8:86375501-86375551	SKMC	muscle:	n/a
42	chr8:86375501-86375551	HRPEpiC	eye:	n/a
43	chr8:86375501-86375551	A549	lung:	n/a
44	chr8:86375501-86375551	PrEC	prostate:	n/a
45	chr8:86375501-86375551	HUVEC	blood vessel:	n/a
46	chr8:86375501-86375551	SK-N-SH	brain:	n/a
47	chr8:86375501-86375551	GM12892	blood:	n/a
48	chr8:86375501-86375551	GM06990	blood:	n/a
49	chr8:86375501-86375551	SAEC	small airway:	n/a
50	chr8:86375501-86375551	MCF10A-Er-Src	breast:	n/a

No.	Distal block	Cell Line	Cell type
1	chr1:144931784..144933992-chr8:86374827..86377261,2	MCF-7	breast:
2	chr8:86348746..86351284-chr8:86374911..86377490,2	MCF-7	breast:
3	chr8:86373793..86376899-chr8:86998896..87001584,3	MCF-7	breast:
4	chr22:36782277..36784307-chr8:86374266..86376495,2	MCF-7	breast:
5	chr8:86375382..86376006-chr8:87045172..87046083,3	MCF-7	breast:
6	chr8:86372229..86378702-chr8:86846475..86858080,32	MCF-7	breast:
7	chr8:86373353..86377706-chr8:86848632..86856784,15	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CA1-1	chr8:86375161-86375671	NONHSAT127527

Variant related genes	Relation type
CA2	TF binding region
ENSG00000253549	TF binding region
CA2	CpG island
ENSG00000253549	CpG island
ENSG00000100345	Chromatin interaction
ENSG00000178104	Chromatin interaction
ENSG00000147614	Chromatin interaction
ENSG00000253154	Chromatin interaction
ENSG00000164879	Chromatin interaction

Extended variants
information (count: 87 )
Associated
traits (count: 3 )

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

rs_ID	r²[population]
rs10087278	0.92[EUR][1000 genomes]
rs10088136	0.87[AMR][1000 genomes];0.91[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs10091566	0.92[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs10095352	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.90[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs10111039	0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs10504812	0.83[CHB][hapmap];0.95[JPT][hapmap];0.81[ASN][1000 genomes]
rs10504813	0.87[CHB][hapmap];1.00[JPT][hapmap];0.85[ASN][1000 genomes]
rs10907474	0.88[CEU][hapmap];0.95[JPT][hapmap];0.85[YRI][hapmap];0.85[AMR][1000 genomes];0.84[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs11261471	0.86[JPT][hapmap]
rs11261474	0.88[CEU][hapmap];0.86[CHB][hapmap];1.00[JPT][hapmap];0.82[EUR][1000 genomes]
rs11780285	0.81[ASN][1000 genomes]
rs11985029	0.92[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs11985733	1.00[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.92[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs12541445	0.86[JPT][hapmap]
rs12543256	0.83[JPT][hapmap]
rs12544332	0.82[CHB][hapmap];0.91[JPT][hapmap]
rs12550814	0.82[EUR][1000 genomes]
rs1303806	0.95[JPT][hapmap]
rs13252971	0.85[CEU][hapmap];0.91[CHB][hapmap];1.00[JPT][hapmap]
rs1390711	0.95[JPT][hapmap]
rs1390712	0.83[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs1493302	0.93[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.81[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs1496529	1.00[JPT][hapmap]
rs1496530	1.00[JPT][hapmap]
rs1496531	0.82[CHB][hapmap];0.91[JPT][hapmap]
rs1496532	0.82[CHB][hapmap];0.91[JPT][hapmap]
rs1532423	0.82[CHB][hapmap];0.95[JPT][hapmap]
rs1532424	0.88[CEU][hapmap];0.86[CHB][hapmap];1.00[JPT][hapmap];0.80[EUR][1000 genomes]
rs1543852	0.82[AMR][1000 genomes];0.93[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs1553015	0.95[JPT][hapmap]
rs16913721	0.91[JPT][hapmap]
rs17042	0.89[CEU][hapmap];0.95[JPT][hapmap]
rs1845253	0.82[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs1908075	0.92[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs1995056	0.90[JPT][hapmap]
rs1995057	0.86[JPT][hapmap]
rs1995058	0.95[JPT][hapmap]
rs2006767	0.91[JPT][hapmap]
rs2055077	0.95[JPT][hapmap]
rs20571	1.00[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.93[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs2072696	0.83[CHB][hapmap];1.00[JPT][hapmap]
rs2279701	0.87[JPT][hapmap]
rs2291787	0.86[JPT][hapmap]
rs2307075	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.91[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2403104	0.95[JPT][hapmap]
rs2548281	0.88[CEU][hapmap];0.95[JPT][hapmap]
rs2645049	0.95[JPT][hapmap]
rs3087782	0.95[JPT][hapmap]
rs3758077	0.91[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs3758078	0.80[CEU][hapmap];0.84[JPT][hapmap];0.86[AMR][1000 genomes];0.84[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs3808539	0.95[JPT][hapmap]
rs4566	1.00[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.86[AMR][1000 genomes];0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs4609189	0.83[JPT][hapmap]
rs4739700	0.91[JPT][hapmap]
rs4740049	0.95[JPT][hapmap]
rs55641432	0.82[ASN][1000 genomes]
rs55929157	0.82[ASN][1000 genomes]
rs58958691	0.81[ASN][1000 genomes]
rs67824746	0.82[ASN][1000 genomes]
rs6988475	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.97[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs6997458	0.82[CHB][hapmap];0.95[JPT][hapmap]
rs7001359	0.87[JPT][hapmap]
rs7011926	0.95[JPT][hapmap]
rs7016369	0.88[CEU][hapmap];0.95[JPT][hapmap];0.85[YRI][hapmap];0.84[AMR][1000 genomes];0.84[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs703	0.86[AMR][1000 genomes];0.94[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs725605	0.83[CEU][hapmap];0.82[CHB][hapmap];0.90[JPT][hapmap]
rs7386162	0.81[ASN][1000 genomes]
rs7818163	0.91[JPT][hapmap]
rs7824715	0.81[EUR][1000 genomes]
rs903895	0.95[JPT][hapmap]
rs903896	0.95[JPT][hapmap]
rs903897	0.95[JPT][hapmap]
rs9286249	0.90[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs931505	0.89[CEU][hapmap];0.95[JPT][hapmap]
rs955007	0.90[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs9969643	1.00[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.90[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs9987281	0.92[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.81[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs999466	0.81[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:9 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1018483	chr8:86142258-86547831	Weak transcription Strong transcription Enhancers Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
2	nsv1022463	chr8:86257031-86547831	Enhancers Weak transcription Strong transcription Bivalent Enhancer Bivalent/Poised TSS Active TSS Flanking Active TSS 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 target site	17 gene(s)	inside rSNPs	diseases
3	esv1804888	chr8:86263098-86986703	Enhancers Weak transcription Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Flanking Active TSS Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	26 gene(s)	inside rSNPs	diseases
4	nsv831377	chr8:86263107-86444141	Flanking Active TSS Enhancers Weak transcription Strong transcription Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	15 gene(s)	inside rSNPs	diseases
5	nsv1028148	chr8:86310570-86553130	Flanking Active TSS Enhancers Weak transcription Strong transcription Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
6	esv2761206	chr8:86310582-86468868	Enhancers Weak transcription Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Active TSS Flanking Active TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	15 gene(s)	inside rSNPs	diseases
7	esv3361413	chr8:86374200-86377398	Bivalent Enhancer Active TSS Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Weak transcription	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
8	esv3394177	chr8:86374925-86377473	Active TSS Flanking Active TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
9	esv3408824	chr8:86375225-86378073	Flanking Active TSS Bivalent Enhancer Enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Weak transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases

mRNA abundance (count:3)

SNP	Gene	Cis/trans	Tissue	Source
rs3758076	CA13	cis	Lymphoblastoid	GTEx
rs3758076	CA2	Cis_1M	lymphoblastoid	RTeQTL
rs3758076	CA2	cis	multi-tissue	Pritchard

Chromatin state (count:105 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:86358400-86375600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr8:86367600-86375600	Weak transcription	Gastric	stomach
3	chr8:86368600-86375600	Weak transcription	Esophagus	oesophagus
4	chr8:86374000-86375600	Enhancers	Stomach Mucosa	stomach
5	chr8:86374400-86375600	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
6	chr8:86375200-86375600	Bivalent/Poised TSS	H1 Cell Line	embryonic stem cell
7	chr8:86375200-86375600	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
8	chr8:86375200-86375600	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
9	chr8:86375200-86375600	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
10	chr8:86375200-86375600	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
11	chr8:86375200-86375600	Enhancers	GM12878-XiMat	blood
12	chr8:86375200-86375800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
13	chr8:86375200-86376200	Active TSS	Primary T helper cells PMA-I stimulated	--
14	chr8:86375200-86376400	Active TSS	ES-I3 Cell Line	embryonic stem cell
15	chr8:86375200-86376400	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
16	chr8:86375200-86376600	Active TSS	Colon Smooth Muscle	Colon
17	chr8:86375200-86376600	Active TSS	A549	lung
18	chr8:86375200-86376800	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
19	chr8:86375200-86376800	Active TSS	Skeletal Muscle Male	skeletal muscle
20	chr8:86375200-86377000	Active TSS	H9 Cell Line	embryonic stem cell
21	chr8:86375200-86377200	Active TSS	ES-WA7 Cell Line	embryonic stem cell
22	chr8:86375200-86377800	Active TSS	Stomach Smooth Muscle	stomach
23	chr8:86375200-86378000	Active TSS	Rectal Smooth Muscle	rectum
24	chr8:86375200-86380200	Active TSS	Rectal Mucosa Donor 29	rectum
25	chr8:86375400-86375600	Bivalent Enhancer	IMR90 fetal lung fibroblasts Cell Line	lung
26	chr8:86375400-86375600	Bivalent/Poised TSS	iPS-18 Cell Line	embryonic stem cell
27	chr8:86375400-86375600	Bivalent/Poised TSS	iPS-20b Cell Line	embryonic stem cell
28	chr8:86375400-86375600	Flanking Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
29	chr8:86375400-86375600	Flanking Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
30	chr8:86375400-86375600	Flanking Active TSS	Breast Myoepithelial Primary Cells	Breast
31	chr8:86375400-86375600	Flanking Active TSS	Primary monocytes fromperipheralblood	blood
32	chr8:86375400-86375600	Flanking Active TSS	Primary B cells from peripheral blood	blood
33	chr8:86375400-86375600	Flanking Active TSS	Primary T cells from cord blood	blood
34	chr8:86375400-86375600	Flanking Bivalent TSS/Enh	Primary T cells fromperipheralblood	blood
35	chr8:86375400-86375600	Flanking Active TSS	Primary T helper memory cells from peripheral blood 2	blood
36	chr8:86375400-86375600	Flanking Active TSS	Primary T helper naive cells from peripheral blood	blood
37	chr8:86375400-86375600	Flanking Active TSS	Primary T helper naive cells fromperipheralblood	blood
38	chr8:86375400-86375600	Flanking Active TSS	Primary T helper 17 cells PMA-I stimulated	--
39	chr8:86375400-86375600	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
40	chr8:86375400-86375600	Flanking Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
41	chr8:86375400-86375600	Flanking Active TSS	Primary Natural Killer cells fromperipheralblood	blood
42	chr8:86375400-86375600	Flanking Active TSS	Primary T killer naive cells fromperipheralblood	blood
43	chr8:86375400-86375600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
44	chr8:86375400-86375600	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
45	chr8:86375400-86375600	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
46	chr8:86375400-86375600	Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
47	chr8:86375400-86375600	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
48	chr8:86375400-86375600	Flanking Active TSS	Adipose Nuclei	Adipose
49	chr8:86375400-86375600	Flanking Active TSS	Liver	Liver
50	chr8:86375400-86375600	Flanking Active TSS	Duodenum Mucosa	Duodenum

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links