Variant report

Variant	rs4875958
Chromosome Location	chr8:1721090-1721091
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	KAP1	chr8:1720855-1721432	HEK293	kidney:	n/a	chr8:1721359-1721367
2	POLR2A	chr8:1720956-1723024	HepG2	liver:	n/a	n/a
3	ZNF263	chr8:1720988-1721561	HEK293-T-REx	kidney:	n/a	n/a
4	GATA3	chr8:1720891-1721373	MCF-7	breast:	n/a	n/a
5	KAP1	chr8:1720934-1721388	U2OS	brain:	n/a	chr8:1721359-1721367
6	NR2F2	chr8:1720924-1721369	MCF-7	breast:	n/a	n/a

Variant related genes	Relation type
CLN8	TF binding region

Extended variants
information (count: 120 )
Associated
traits (count: 4 )

rSNPs within LD-proxies of this variant (count:97)

rs_ID	r²[population]
rs10087654	0.91[ASN][1000 genomes]
rs10089222	0.92[AMR][1000 genomes];0.83[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs10097891	0.93[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];0.89[GIH][hapmap];0.94[JPT][hapmap];0.92[LWK][hapmap];0.96[MEX][hapmap];0.92[MKK][hapmap];0.92[TSI][hapmap];0.87[AFR][1000 genomes];0.99[AMR][1000 genomes];0.97[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs10100341	0.87[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];0.93[GIH][hapmap];0.94[JPT][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];0.93[MKK][hapmap];1.00[TSI][hapmap];0.91[YRI][hapmap];0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs10102731	0.91[ASN][1000 genomes]
rs10105317	0.88[CHB][hapmap];0.82[GIH][hapmap];0.94[JPT][hapmap];0.85[ASN][1000 genomes]
rs10106153	0.85[ASN][1000 genomes]
rs10113471	0.80[ASN][1000 genomes]
rs10481354	0.88[CHB][hapmap];0.82[GIH][hapmap];1.00[JPT][hapmap];0.91[MEX][hapmap];0.81[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs11136421	0.81[CHB][hapmap];0.82[GIH][hapmap];0.94[JPT][hapmap];0.81[ASN][1000 genomes]
rs11136422	0.81[ASN][1000 genomes]
rs11136424	0.81[CEU][hapmap];1.00[CHB][hapmap];0.85[GIH][hapmap];1.00[JPT][hapmap];0.96[MEX][hapmap];0.83[TSI][hapmap];0.93[AMR][1000 genomes];0.89[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1137514	0.81[AMR][1000 genomes]
rs11778824	0.94[CHB][hapmap];0.89[JPT][hapmap];0.91[ASN][1000 genomes]
rs12335115	0.85[ASN][1000 genomes]
rs12674711	0.83[ASN][1000 genomes]
rs13251071	0.81[ASN][1000 genomes]
rs13256424	0.96[AMR][1000 genomes];0.94[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs13261755	0.82[ASN][1000 genomes]
rs13282161	0.82[ASN][1000 genomes]
rs13540	0.90[ASN][1000 genomes]
rs2293977	0.94[CHB][hapmap];0.94[JPT][hapmap];0.89[ASN][1000 genomes]
rs28376731	0.84[ASN][1000 genomes]
rs2957085	0.81[CHB][hapmap];0.82[GIH][hapmap];0.94[JPT][hapmap];0.81[ASN][1000 genomes]
rs35062922	0.81[ASN][1000 genomes]
rs3812477	0.94[CHB][hapmap];1.00[JPT][hapmap];0.88[AMR][1000 genomes];0.81[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs4242538	0.86[CHB][hapmap];0.94[JPT][hapmap];0.82[ASN][1000 genomes]
rs4242539	0.81[CHB][hapmap];0.94[JPT][hapmap]
rs4370560	0.94[CHB][hapmap];1.00[JPT][hapmap];0.90[ASN][1000 genomes]
rs4372027	0.90[ASN][1000 genomes]
rs4595147	0.88[CHB][hapmap];1.00[JPT][hapmap];0.96[MEX][hapmap];0.86[ASN][1000 genomes]
rs4639549	0.91[CHB][hapmap];1.00[JPT][hapmap];0.90[ASN][1000 genomes]
rs4875806	0.96[ASN][1000 genomes]
rs4875889	0.80[ASN][1000 genomes]
rs4875957	0.96[ASN][1000 genomes]
rs6558518	0.84[ASN][1000 genomes]
rs6558520	0.88[CHB][hapmap];0.82[GIH][hapmap];0.94[JPT][hapmap];0.84[ASN][1000 genomes]
rs6558521	0.88[CHB][hapmap];0.82[GIH][hapmap];0.94[JPT][hapmap];0.85[ASN][1000 genomes]
rs6558522	0.88[CHB][hapmap];0.82[GIH][hapmap];0.94[JPT][hapmap];0.85[ASN][1000 genomes]
rs6558523	0.87[CHB][hapmap];0.93[JPT][hapmap];0.85[ASN][1000 genomes]
rs6558524	0.85[ASN][1000 genomes]
rs6558525	0.88[CHB][hapmap];0.94[JPT][hapmap];0.85[ASN][1000 genomes]
rs6558526	0.84[ASN][1000 genomes]
rs6558527	0.81[CHB][hapmap];0.94[JPT][hapmap];0.85[ASN][1000 genomes]
rs6558528	0.84[ASN][1000 genomes]
rs6558530	0.81[ASN][1000 genomes]
rs6558531	0.90[ASN][1000 genomes]
rs6558532	0.90[ASN][1000 genomes]
rs6558533	0.94[CHB][hapmap];0.82[GIH][hapmap];1.00[JPT][hapmap];0.91[ASN][1000 genomes]
rs6558534	0.90[CHB][hapmap];1.00[JPT][hapmap];0.92[ASN][1000 genomes]
rs6558535	0.92[ASN][1000 genomes]
rs6558538	0.85[ASN][1000 genomes]
rs6981804	0.85[ASN][1000 genomes]
rs6982516	0.96[ASN][1000 genomes]
rs6984632	0.83[ASN][1000 genomes]
rs6986102	0.87[CHB][hapmap];1.00[JPT][hapmap];0.84[ASN][1000 genomes]
rs6991773	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs6991783	0.94[ASN][1000 genomes]
rs6993706	0.94[CHB][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.96[ASN][1000 genomes]
rs7000162	0.89[AMR][1000 genomes];0.87[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7001282	0.85[ASN][1000 genomes]
rs7005592	0.81[CHB][hapmap];0.82[GIH][hapmap];0.94[JPT][hapmap];0.85[ASN][1000 genomes]
rs7005699	0.86[CHB][hapmap];0.94[JPT][hapmap];0.85[ASN][1000 genomes]
rs7008465	0.94[CHB][hapmap];0.96[GIH][hapmap];0.94[JPT][hapmap];0.95[ASN][1000 genomes]
rs7010616	0.84[ASN][1000 genomes]
rs7013835	0.81[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs7013841	0.83[ASN][1000 genomes]
rs7014327	0.93[ASW][hapmap];0.96[CEU][hapmap];1.00[CHB][hapmap];0.92[GIH][hapmap];0.94[JPT][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.83[YRI][hapmap];0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7014823	0.94[ASN][1000 genomes]
rs7015858	0.96[CEU][hapmap];1.00[CHB][hapmap];0.94[JPT][hapmap];0.96[AMR][1000 genomes];0.93[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs71499040	0.91[ASN][1000 genomes]
rs730377	0.82[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs730379	0.81[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs7341635	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7459507	0.83[ASN][1000 genomes]
rs7460230	0.82[ASN][1000 genomes]
rs7460287	0.93[CHB][hapmap];1.00[JPT][hapmap];0.90[ASN][1000 genomes]
rs7460365	0.84[ASN][1000 genomes]
rs7460866	0.85[ASN][1000 genomes]
rs7460972	0.93[JPT][hapmap];0.90[ASN][1000 genomes]
rs7461159	0.81[CEU][hapmap];1.00[CHB][hapmap];0.82[GIH][hapmap];1.00[JPT][hapmap];0.96[MEX][hapmap];0.83[TSI][hapmap];0.93[AMR][1000 genomes];0.89[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7461259	0.82[ASN][1000 genomes]
rs7461600	0.91[AMR][1000 genomes];0.85[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7463876	0.89[ASN][1000 genomes]
rs7463879	0.87[ASN][1000 genomes]
rs7465178	0.93[ASN][1000 genomes]
rs7818406	0.87[CHB][hapmap];0.94[JPT][hapmap];0.85[ASN][1000 genomes]
rs7822816	0.89[ASN][1000 genomes]
rs7827009	0.94[CHB][hapmap];1.00[JPT][hapmap];0.92[ASN][1000 genomes]
rs7827285	0.94[CHB][hapmap];1.00[JPT][hapmap];0.92[ASN][1000 genomes]
rs7828950	0.89[ASN][1000 genomes]
rs7838456	0.90[ASN][1000 genomes]
rs7842425	0.88[CHB][hapmap];0.82[GIH][hapmap];1.00[JPT][hapmap];0.91[MEX][hapmap];0.81[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs7844748	0.88[CHB][hapmap];0.81[GIH][hapmap];0.94[JPT][hapmap];0.85[ASN][1000 genomes]
rs7845723	0.87[CHB][hapmap];0.82[GIH][hapmap];0.89[JPT][hapmap]
rs7846610	0.88[CHB][hapmap];0.82[GIH][hapmap];1.00[JPT][hapmap];0.91[MEX][hapmap];0.89[ASN][1000 genomes]
rs9022	0.89[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	nsv889697	chr8:1238564-1861971	Flanking Active TSS Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Weak transcription Enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	17 gene(s)	inside rSNPs	diseases
2	nsv1031375	chr8:1320657-1722050	Enhancers Weak transcription Strong transcription Bivalent Enhancer Active TSS Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
3	nsv889704	chr8:1563904-1965389	Flanking Active TSS Enhancers Genic enhancers Strong transcription Weak transcription Active TSS ZNF genes & repeats Bivalent Enhancer 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	18 gene(s)	inside rSNPs	diseases
4	nsv889707	chr8:1581839-1920461	Enhancers Active TSS Weak transcription Genic enhancers Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
5	nsv889708	chr8:1581839-1965389	Genic enhancers Strong transcription Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	17 gene(s)	inside rSNPs	diseases
6	nsv889709	chr8:1581839-1965389	Active TSS Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	17 gene(s)	inside rSNPs	diseases
7	nsv889711	chr8:1591412-1904157	Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	14 gene(s)	inside rSNPs	diseases
8	nsv889712	chr8:1591412-2337777	Weak transcription Active TSS Strong transcription Enhancers ZNF genes & repeats Bivalent Enhancer Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	22 gene(s)	inside rSNPs	diseases
9	nsv889714	chr8:1616718-1965389	Enhancers Weak transcription Strong transcription Bivalent/Poised TSS Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	17 gene(s)	inside rSNPs	diseases
10	nsv934075	chr8:1626857-1736355	Weak transcription Enhancers Genic enhancers Flanking Active TSS Strong transcription Active TSS Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
11	nsv1034490	chr8:1654716-1782467	Strong transcription Enhancers Flanking Active TSS Weak transcription Active TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	10 gene(s)	inside rSNPs	diseases
12	nsv609527	chr8:1681733-1753497	Weak transcription Enhancers Genic enhancers Flanking Active TSS Active TSS Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	8 gene(s)	inside rSNPs	diseases
13	nsv870096	chr8:1682851-1767342	Strong transcription Enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	9 gene(s)	inside rSNPs	diseases
14	nsv465274	chr8:1685064-1728292	Flanking Active TSS Enhancers Active TSS Weak transcription Bivalent Enhancer Strong transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
15	nsv609528	chr8:1685064-1728292	Enhancers Weak transcription Active TSS Strong transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
16	nsv532892	chr8:1687433-1839578	Weak transcription Bivalent Enhancer Flanking Active TSS Enhancers Active TSS Strong transcription Genic enhancers 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	11 gene(s)	inside rSNPs	diseases
17	esv2755149	chr8:1689290-1755281	Enhancers Active TSS Strong transcription Flanking Active TSS Weak transcription Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	8 gene(s)	inside rSNPs	diseases
18	nsv465275	chr8:1697086-1768004	Weak transcription Flanking Active TSS Active TSS Genic enhancers Enhancers Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	9 gene(s)	inside rSNPs	diseases
19	nsv609529	chr8:1697086-1768004	Weak transcription Enhancers Genic enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Strong transcription Active TSS Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	9 gene(s)	inside rSNPs	diseases
20	nsv465276	chr8:1701432-1777571	Active TSS Enhancers Flanking Active TSS Weak transcription Genic enhancers Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	10 gene(s)	inside rSNPs	diseases
21	nsv609530	chr8:1701432-1777571	Active TSS Flanking Active TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Genic enhancers Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	10 gene(s)	inside rSNPs	diseases
22	nsv609531	chr8:1717036-1965389	Weak transcription Active TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Enhancers Strong transcription Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	12 gene(s)	inside rSNPs	diseases
23	nsv932825	chr8:1719042-1736355	Enhancers Weak transcription Genic enhancers Strong transcription ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases

mRNA abundance (count:4)

SNP	Gene	Cis/trans	Tissue	Source
rs4875958	CTD-2336O2.1	cis	Adipose Subcutaneous	GTEx
rs4875958	CTD-2336O2.1	cis	Nerve Tibial	GTEx
rs4875958	C8orf61	cis	multi-tissue	Pritchard
rs4875958	CLN8	cis	multi-tissue	Pritchard

Chromatin state (count:127 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:1713400-1727000	Weak transcription	NHDF-Ad	bronchial
2	chr8:1713400-1735800	Weak transcription	Fetal Brain Male	brain
3	chr8:1713600-1721400	Weak transcription	Rectal Smooth Muscle	rectum
4	chr8:1713600-1729600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
5	chr8:1714000-1728000	Weak transcription	Pancreatic Islets	Pancreatic Islet
6	chr8:1714000-1729800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
7	chr8:1714400-1729200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
8	chr8:1714800-1727000	Strong transcription	Fetal Intestine Small	intestine
9	chr8:1715400-1726800	Strong transcription	Fetal Stomach	stomach
10	chr8:1715400-1727800	Weak transcription	Small Intestine	intestine
11	chr8:1715400-1729200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
12	chr8:1715600-1725600	Strong transcription	Rectal Mucosa Donor 29	rectum
13	chr8:1716400-1726800	Strong transcription	Monocytes-CD14+_RO01746	blood
14	chr8:1716600-1723000	Strong transcription	Primary hematopoietic stem cells short term culture	blood
15	chr8:1716600-1725200	Strong transcription	Duodenum Mucosa	Duodenum
16	chr8:1716600-1727000	Strong transcription	Primary monocytes fromperipheralblood	blood
17	chr8:1716800-1721200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
18	chr8:1716800-1722000	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
19	chr8:1717000-1724600	Strong transcription	Primary T cells fromperipheralblood	blood
20	chr8:1717000-1724600	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
21	chr8:1717200-1722400	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
22	chr8:1717400-1728400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
23	chr8:1717600-1722000	Weak transcription	HSMMtube	muscle
24	chr8:1717600-1724600	Strong transcription	HMEC	breast
25	chr8:1717600-1726400	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
26	chr8:1717600-1731000	Weak transcription	Fetal Lung	lung
27	chr8:1717800-1722400	Strong transcription	NHEK	skin
28	chr8:1717800-1724600	Strong transcription	HUES6 Cell Line	embryonic stem cell
29	chr8:1717800-1725000	Weak transcription	HSMM	muscle
30	chr8:1717800-1725200	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
31	chr8:1717800-1726200	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
32	chr8:1717800-1726200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
33	chr8:1717800-1727800	Weak transcription	Stomach Mucosa	stomach
34	chr8:1718000-1721200	Weak transcription	Right Atrium	heart
35	chr8:1718000-1722000	Strong transcription	HepG2	liver
36	chr8:1718000-1722400	Strong transcription	HUES48 Cell Line	embryonic stem cell
37	chr8:1718000-1726000	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
38	chr8:1718000-1726600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
39	chr8:1718000-1727800	Weak transcription	Fetal Kidney	kidney
40	chr8:1718000-1728000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
41	chr8:1718000-1732400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
42	chr8:1718000-1732800	Weak transcription	Fetal Heart	heart
43	chr8:1718000-1736000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
44	chr8:1718200-1721400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
45	chr8:1718200-1721600	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
46	chr8:1718200-1724000	Weak transcription	Brain Angular Gyrus	brain
47	chr8:1718400-1724000	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
48	chr8:1718400-1725000	Strong transcription	Fetal Intestine Large	intestine
49	chr8:1718400-1733200	Weak transcription	Placenta Amnion	Placenta Amnion
50	chr8:1718800-1721800	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood

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